SomamiR DB 2.0
Somatic mutations altering microRNA-ceRNA interactions
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PolymiRTS Database
Prediction criteria: TargetScan sites only     All 6mer or longer seed matches
Transcript ID: NM_002160
Gene Symbol: TNC
Browse Associations
Browse Pathways

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115091013G>A COSM3926042 TCGA-FW-A3R5-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2116-3p ccATGGGAGccatga CCUCCCAU m7b (m6b->m7b) HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-874-5p ccatgGGGGCCatga CGGCCCCA m6b Disrupted HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-2116-3p ccATGGGAGccatga CCUCCCAU m7b (m6b->m7b) HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-874-5p ccatgGGGGCCatga CGGCCCCA m6b Disrupted HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090974C>T COSM3653443 TCGA-EE-A29M-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-31-5p ttgctttTCTTGCCc AGGCAAGA m7b Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-651-3p ttgcTTTCCTTgccc AAAGGAAA m7b Disrupted HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6809-5p ttgctttCCTTGCCc UGGCAAGG m7b Disrupted HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6830-5p ttgctTTCCTTGccc CCAAGGAA m7b Disrupted HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-31-5p ttgctttTCTTGCCc AGGCAAGA m7b Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-651-3p ttgcTTTCCTTgccc AAAGGAAA m7b Disrupted HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6809-5p ttgctttCCTTGCCc UGGCAAGG m7b Disrupted HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6830-5p ttgctTTCCTTGccc CCAAGGAA m7b Disrupted HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090972T>G COSM1268196 ESO-0280 [oesophagus][lower_third][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-564 gctttCCGTGCCctc AGGCACGG m7b Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-651-3p gcTTTCCTTgccctc AAAGGAAA m7b (m7b->m6b) HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6809-5p gctttCCTTGCCctc UGGCAAGG m7b Disrupted HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6830-5p gctTTCCTTGccctc CCAAGGAA m7b Disrupted HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-564 gctttCCGTGCCctc AGGCACGG m7b Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-651-3p gcTTTCCTTgccctc AAAGGAAA m7b (m7b->m6b) HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6809-5p gctttCCTTGCCctc UGGCAAGG m7b Disrupted HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6830-5p gctTTCCTTGccctc CCAAGGAA m7b Disrupted HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090959C>T COSM3395518 8016470 [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-199a-3p tcgCTACTGaaggtg ACAGUAGU m6b Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-199b-3p tcgCTACTGaaggtg ACAGUAGU m6b Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-222-5p tcgCTACTGAaggtg CUCAGUAG m7b Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-3129-5p tcgCTACTGaaggtg GCAGUAGU m6b Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-936 tcgCTACTGaaggtg ACAGUAGA m6b Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-199a-3p tcgCTACTGaaggtg ACAGUAGU m6b Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-199b-3p tcgCTACTGaaggtg ACAGUAGU m6b Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-222-5p tcgCTACTGAaggtg CUCAGUAG m7b Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-3129-5p tcgCTACTGaaggtg GCAGUAGU m6b Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-936 tcgCTACTGaaggtg ACAGUAGA m6b Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090953T>G COSM3847468 TCGA-A2-A0T5-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1224-3p ccgaAGGTGGGGtcc CCCCACCU m8a Disrupted HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-3127-3p ccGAAGGGGgggtcc UCCCCUUC m7b (m6b->m7b) HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6756-3p ccGAAGGGGgggtcc UCCCCUUC m7b (m6b->m7b) HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6859-3p ccgaaggGGGGGTCc UGACCCCC m7b Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-1224-3p ccgaAGGTGGGGtcc CCCCACCU m8a Disrupted HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-3127-3p ccGAAGGGGgggtcc UCCCCUUC m7b (m6b->m7b) HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6756-3p ccGAAGGGGgggtcc UCCCCUUC m7b (m6b->m7b) HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-6859-3p ccgaaggGGGGGTCc UGACCCCC m7b Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090938A>T COSM751900 TCGA-22-4604-01 [lung][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4262 tcaaGAATGTCatcc GACAUUCA m7a Created HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-4262 tcaaGAATGTCatcc GACAUUCA m7a Created HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090927A>G COSM3664032 HX30T [liver][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3195 atCCGGCGCaagcga CGCGCCGG m7b (m6b->m7b) HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-550b-2-5p atccGGCACAagcga AUGUGCCU m6b Disrupted HHHNA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-3195 atCCGGCGCaagcga CGCGCCGG m7b (m6b->m7b) HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422
hsa-miR-550b-2-5p atccGGCACAagcga AUGUGCCU m6b Disrupted HHHSA_22281_TNC|NM_002160|exon_utr5|-7.23104912400915|1.0940425752422

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090893A>G COSM1459592 TCGA-AZ-6601-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4664-3p ccctgCCGGAAGaga CUUCCGGU m7a Created HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4720-5p cccTGCCAGaagaga CCUGGCAU m6b Disrupted HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4799-3p cccTGCCAGaagaga ACUGGCAU m6b Disrupted HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-5588-5p cccTGCCAGaagaga ACUGGCAU m6b Disrupted HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-6868-5p ccCTGCCAGaagaga ACUGGCAG m7b (m7b->m6b) HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-7150 cCCTGCCAGaagaga CUGGCAGG m8a (m8a->m7a) HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-1180-3p ccctGCCGGAAgaga UUUCCGGC m7b Created HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-1207-5p CCCTGCCAgaagaga UGGCAGGG m8a Disrupted HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-1236-3p ccctgccGGAAGAGa CCUCUUCC m7b Created HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-3128 cccTGCCAGAagaga UCUGGCAA m7a Disrupted HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-3182 ccctgcCAGAAGaga GCUUCUGU m6b Disrupted HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4664-3p ccctgCCGGAAGaga CUUCCGGU m7a Created HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4720-5p cccTGCCAGaagaga CCUGGCAU m6b Disrupted HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4799-3p cccTGCCAGaagaga ACUGGCAU m6b Disrupted HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-5588-5p cccTGCCAGaagaga ACUGGCAU m6b Disrupted HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-6868-5p ccCTGCCAGaagaga ACUGGCAG m7b (m7b->m6b) HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-7150 cCCTGCCAGaagaga CUGGCAGG m8a (m8a->m7a) HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-1180-3p ccctGCCGGAAgaga UUUCCGGC m7b Created HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-1207-5p CCCTGCCAgaagaga UGGCAGGG m8a Disrupted HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-1236-3p ccctgccGGAAGAGa CCUCUUCC m7b Created HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-3128 cccTGCCAGAagaga UCUGGCAA m7a Disrupted HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-3182 ccctgcCAGAAGaga GCUUCUGU m6b Disrupted HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090873T>C COSM3903462 TCGA-CG-5721-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-21-3p ccagTGGTGTTtaac CAACACCA m7b Disrupted HHFCT_158263_cluster-23497_17_12
hsa-miR-3591-3p ccagTGGTGTTTaac AAACACCA m8a Disrupted HHFCT_158263_cluster-23497_17_12
hsa-miR-4252 cCAGTGGCgtttaac GGCCACUG m7b Created HHFCT_158263_cluster-23497_17_12
hsa-miR-21-3p ccagTGGTGTTtaac CAACACCA m7b Disrupted HHHNE_19286_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-3591-3p ccagTGGTGTTTaac AAACACCA m8a Disrupted HHHNE_19286_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4252 cCAGTGGCgtttaac GGCCACUG m7b Created HHHNE_19286_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-21-3p ccagTGGTGTTtaac CAACACCA m7b Disrupted HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-3591-3p ccagTGGTGTTTaac AAACACCA m8a Disrupted HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4252 cCAGTGGCgtttaac GGCCACUG m7b Created HHHNE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-21-3p ccagTGGTGTTtaac CAACACCA m7b Disrupted HHHSE_19286_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-3591-3p ccagTGGTGTTTaac AAACACCA m8a Disrupted HHHSE_19286_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4252 cCAGTGGCgtttaac GGCCACUG m7b Created HHHSE_19286_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-21-3p ccagTGGTGTTtaac CAACACCA m7b Disrupted HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-3591-3p ccagTGGTGTTTaac AAACACCA m8a Disrupted HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-4252 cCAGTGGCgtttaac GGCCACUG m7b Created HHHSE_19287_TNC|NM_002160|exon_CDS|-8.43866880485331|-1.12427816906537
hsa-miR-21-3p ccagTGGTGTTtaac CAACACCA m7b Disrupted HHKTA_51677_NM_002160|501|540|1.29803823155271|0.103901125677711
hsa-miR-3591-3p ccagTGGTGTTTaac AAACACCA m8a Disrupted HHKTA_51677_NM_002160|501|540|1.29803823155271|0.103901125677711
hsa-miR-4252 cCAGTGGCgtttaac GGCCACUG m7b Created HHKTA_51677_NM_002160|501|540|1.29803823155271|0.103901125677711

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090840T>C COSM1459591 TCGA-CA-6718-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3156-3p ctgccAGTGGGAtcc CUCCCACU m7b Disrupted HHKTA_51677_NM_002160|501|540|1.29803823155271|0.103901125677711

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090783C>T COSM1459590 TCGA-F4-6703-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2682-5p ctggcACTGCCTtca CAGGCAGU m7b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-34a-5p ctggCACTGCCttca UGGCAGUG m7b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-34b-5p ctggcACTGCCTtca UAGGCAGU m7b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-34c-5p ctggCACTGCCTtca AGGCAGUG m8a Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-3714 ctggcaCTGCCTTCa GAAGGCAG m8a Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-449a ctggCACTGCCttca UGGCAGUG m7b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-449b-5p ctggCACTGCCTtca AGGCAGUG m8a Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-449c-5p ctggcACTGCCTtca UAGGCAGU m7b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-4746-3p ctgGCACCGCcttca AGCGGUGC m7b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-524-3p ctggcacCGCCTTCa GAAGGCGC m7a Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-525-3p ctggcacCGCCTTCa GAAGGCGC m7a Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-605-3p ctggcacTGCCTTCa AGAAGGCA m7b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-2682-5p ctggcACTGCCTtca CAGGCAGU m7b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-34a-5p ctggCACTGCCttca UGGCAGUG m7b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-34b-5p ctggcACTGCCTtca UAGGCAGU m7b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-34c-5p ctggCACTGCCTtca AGGCAGUG m8a Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-3714 ctggcaCTGCCTTCa GAAGGCAG m8a Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-449a ctggCACTGCCttca UGGCAGUG m7b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-449b-5p ctggCACTGCCTtca AGGCAGUG m8a Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-449c-5p ctggcACTGCCTtca UAGGCAGU m7b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-4746-3p ctgGCACCGCcttca AGCGGUGC m7b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-524-3p ctggcacCGCCTTCa GAAGGCGC m7a Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-525-3p ctggcacCGCCTTCa GAAGGCGC m7a Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-605-3p ctggcacTGCCTTCa AGAAGGCA m7b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090782G>A COSM300256 TCGA-AA-A01T-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4493 tggcaccGCCTTCag AGAAGGCC m6b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-4746-3p tgGCACCGCcttcag AGCGGUGC m7b (m7b->m6b) HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-524-3p tggcacCGCCTTCag GAAGGCGC m7a Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-525-3p tggcacCGCCTTCag GAAGGCGC m7a Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-605-3p tggcaccGCCTTCag AGAAGGCA m6b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6126 tggcaccGCCTTCAg GUGAAGGC m7b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-4493 tggcaccGCCTTCag AGAAGGCC m6b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-4746-3p tgGCACCGCcttcag AGCGGUGC m7b (m7b->m6b) HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-524-3p tggcacCGCCTTCag GAAGGCGC m7a Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-525-3p tggcacCGCCTTCag GAAGGCGC m7a Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-605-3p tggcaccGCCTTCag AGAAGGCA m6b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6126 tggcaccGCCTTCAg GUGAAGGC m7b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090769A>T COSM751902 TCGA-34-5231-01 [lung][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1909-3p agagCCCTGCGaaag CGCAGGGG m7a Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-378g agAGCCCAGcgaaag ACUGGGCU m7b (m7b->m6b) HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-4674 aGAGCCCAGcgaaag CUGGGCUC m8a (m8a->m7a) HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-5088-5p aGAGCCCTGcgaaag CAGGGCUC m8a (m7a->m8a) HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6132 agaGCCCTGCgaaag AGCAGGGC m7b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-639 agagccCAGCGAaag AUCGCUGC m6b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6836-5p agaGCCCTGCGaaag CGCAGGGC m8a Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-1909-3p agagCCCTGCGaaag CGCAGGGG m7a Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-378g agAGCCCAGcgaaag ACUGGGCU m7b (m7b->m6b) HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-4674 aGAGCCCAGcgaaag CUGGGCUC m8a (m8a->m7a) HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-5088-5p aGAGCCCTGcgaaag CAGGGCUC m8a (m7a->m8a) HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6132 agaGCCCTGCgaaag AGCAGGGC m7b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-639 agagccCAGCGAaag AUCGCUGC m6b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6836-5p agaGCCCTGCGaaag CGCAGGGC m8a Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090743G>A COSM150690 GC8_T [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1273g-3p acaCAGTGGatgggg ACCACUGC m6b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-181a-2-3p acaCAGTGGatgggg ACCACUGA m6b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6509-3p acaCAGTGGAtgggg UUCCACUG m7b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-1273g-3p acaCAGTGGatgggg ACCACUGC m6b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-181a-2-3p acaCAGTGGatgggg ACCACUGA m6b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6509-3p acaCAGTGGAtgggg UUCCACUG m7b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090739G>T COSM3675219 TCGA-G9-6342-01 [prostate][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2355-5p agtggaTGGGGAaaa AUCCCCAG m6b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-3679-3p agtggatGGGGAAaa CUUCCCCC m6b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-2355-5p agtggaTGGGGAaaa AUCCCCAG m6b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-3679-3p agtggatGGGGAAaa CUUCCCCC m6b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090720T>C COSM1104468 TCGA-BS-A0UV-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-644a attgtctCCACACat AGUGUGGC m6b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6818-5p attgtctTCACACAt UUGUGUGA m7b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6833-5p attgtcTCCACACat GUGUGGAA m7a Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-7847-3p attgtCTCCACacat CGUGGAGG m6b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-147a attgtctCCACACAt GUGUGUGG m7b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-3611 attgtCTTCACAcat UUGUGAAG m7b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-3911 attgtcTCCACACAt UGUGUGGA m8a Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-644a attgtctCCACACat AGUGUGGC m6b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6818-5p attgtctTCACACAt UUGUGUGA m7b Disrupted HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-6833-5p attgtcTCCACACat GUGUGGAA m7a Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-7847-3p attgtCTCCACacat CGUGGAGG m6b Created HHHSA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-147a attgtctCCACACAt GUGUGUGG m7b Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-3611 attgtCTTCACAcat UUGUGAAG m7b Disrupted HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411
hsa-miR-3911 attgtcTCCACACAt UGUGUGGA m8a Created HHHNA_22280_TNC|NM_002160|exon_CDS|-7.95286410989683|0.618785180718411

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090677C>T COSM1104467 TCGA-B5-A11E-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-103a-3p gctgTGCTGCagccc AGCAGCAU m6b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-107 gctgTGCTGCagccc AGCAGCAU m6b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-1184 gctgtGCTGCAGccc CCUGCAGC m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-604 gctgtgcCGCAGCCc AGGCUGCG m7b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-103a-3p gctgTGCTGCagccc AGCAGCAU m6b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-107 gctgTGCTGCagccc AGCAGCAU m6b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-1184 gctgtGCTGCAGccc CCUGCAGC m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-604 gctgtgcCGCAGCCc AGGCUGCG m7b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090676G>A COSM3382406 PCSI_0112_Pa_P [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3688-5p ctgTGCCACagcccc AGUGGCAA m6b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4675 ctgtgccACAGCCCc GGGGCUGU m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4741 ctgtgccACAGCCCc CGGGCUGU m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-604 ctgtgcCGCAGCCcc AGGCUGCG m7b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6829-5p ctgtgccGCAGCCCc UGGGCUGC m7b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-7974 ctgtgcCACAGCCcc AGGCUGUG m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-891a-3p ctGTGCCACagcccc AGUGGCAC m7b (m6b->m7b) HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-3688-5p ctgTGCCACagcccc AGUGGCAA m6b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4675 ctgtgccACAGCCCc GGGGCUGU m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4741 ctgtgccACAGCCCc CGGGCUGU m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-604 ctgtgcCGCAGCCcc AGGCUGCG m7b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6829-5p ctgtgccGCAGCCCc UGGGCUGC m7b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-7974 ctgtgcCACAGCCcc AGGCUGUG m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-891a-3p ctGTGCCACagcccc AGUGGCAC m7b (m6b->m7b) HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090672C>T COSM3382405 PCSI_0090_Pa_P [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1288-3p gccGCAGTCCctgat UGGACUGC m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-185-3p gccgCAGCCCCTgat AGGGGCUG m8a Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-211-3p gccgcaGTCCCTGat GCAGGGAC m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-3199 gccgCAGTCCCTgat AGGGACUG m8a Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4441 gccgcagTCCCTGat ACAGGGAG m6b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-604 gcCGCAGCCcctgat AGGCUGCG m7b (m7b->m6b) HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6085 gccgcAGCCCCTgat AAGGGGCU m7b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6754-5p gccgcagTCCCTGat CCAGGGAG m6b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6798-5p gccgcagCCCCTGat CCAGGGGG m6b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6813-5p gccgcAGCCCCTGat CAGGGGCU m8a Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6829-5p gccGCAGCCCctgat UGGGCUGC m7b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-8052 gccgCAGTCCCtgat CGGGACUG m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-1288-3p gccGCAGTCCctgat UGGACUGC m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-185-3p gccgCAGCCCCTgat AGGGGCUG m8a Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-211-3p gccgcaGTCCCTGat GCAGGGAC m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-3199 gccgCAGTCCCTgat AGGGACUG m8a Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4441 gccgcagTCCCTGat ACAGGGAG m6b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-604 gcCGCAGCCcctgat AGGCUGCG m7b (m7b->m6b) HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6085 gccgcAGCCCCTgat AAGGGGCU m7b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6754-5p gccgcagTCCCTGat CCAGGGAG m6b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6798-5p gccgcagCCCCTGat CCAGGGGG m6b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6813-5p gccgcAGCCCCTGat CAGGGGCU m8a Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6829-5p gccGCAGCCCctgat UGGGCUGC m7b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-8052 gccgCAGTCCCtgat CGGGACUG m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090671C>T COSM4489512 CSCC-20-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-185-3p ccgCAGCCCCTgatg AGGGGCUG m8a Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-28-5p ccgcAGCTCCTgatg AAGGAGCU m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-3139 ccgcAGCTCCTgatg UAGGAGCU m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4433a-3p ccgcagCTCCTGatg ACAGGAGU m6b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4459 ccgcagCTCCTGatg CCAGGAGG m6b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4768-3p ccgcagCTCCTGatg CCAGGAGA m6b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-558 ccGCAGCTCctgatg UGAGCUGC m7b (m6b->m7b) HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-604 cCGCAGCCcctgatg AGGCUGCG m7b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6085 ccgcAGCCCCTgatg AAGGGGCU m7b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6798-5p ccgcagCCCCTGatg CCAGGGGG m6b Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6813-5p ccgcAGCCCCTGatg CAGGGGCU m8a Disrupted HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6829-5p ccGCAGCCCctgatg UGGGCUGC m7b (m7b->m6b) HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-708-5p ccgcAGCTCCTgatg AAGGAGCU m7b Created HHHNE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-185-3p ccgCAGCCCCTgatg AGGGGCUG m8a Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-28-5p ccgcAGCTCCTgatg AAGGAGCU m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-3139 ccgcAGCTCCTgatg UAGGAGCU m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4433a-3p ccgcagCTCCTGatg ACAGGAGU m6b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4459 ccgcagCTCCTGatg CCAGGAGG m6b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-4768-3p ccgcagCTCCTGatg CCAGGAGA m6b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-558 ccGCAGCTCctgatg UGAGCUGC m7b (m6b->m7b) HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-604 cCGCAGCCcctgatg AGGCUGCG m7b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6085 ccgcAGCCCCTgatg AAGGGGCU m7b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6798-5p ccgcagCCCCTGatg CCAGGGGG m6b Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6813-5p ccgcAGCCCCTGatg CAGGGGCU m8a Disrupted HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-6829-5p ccGCAGCCCctgatg UGGGCUGC m7b (m7b->m6b) HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345
hsa-miR-708-5p ccgcAGCTCCTgatg AAGGAGCU m7b Created HHHSE_19285_TNC|NM_002160|exon_CDS|-7.91844067332968|0.35899525568345

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090656G>A COSM3653440 TCGA-D3-A2JF-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-584-3p ttaaGGAACTGctga UCAGUUCC m7b Created HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-646 ttaaggAGCTGCTga AAGCAGCU m7b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-6736-3p ttaaGGAGCTGctga UCAGCUCC m7b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-424-5p ttaaggaGCTGCTGa CAGCAGCA m7a Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4274 ttaaggaACTGCTGa CAGCAGUC m7a Created HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4448 ttAAGGAGCtgctga GGCUCCUU m7b (m7b->m6b) HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4519 ttaaggaACTGCTGa CAGCAGUG m7a Created HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4660 ttaagGAGCTGCtga UGCAGCUC m7b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-497-5p ttaaggaGCTGCTGa CAGCAGCA m7a Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-584-3p ttaaGGAACTGctga UCAGUUCC m7b Created HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-646 ttaaggAGCTGCTga AAGCAGCU m7b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-6736-3p ttaaGGAGCTGctga UCAGCUCC m7b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-424-5p ttaaggaGCTGCTGa CAGCAGCA m7a Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4274 ttaaggaACTGCTGa CAGCAGUC m7a Created HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4448 ttAAGGAGCtgctga GGCUCCUU m7b (m7b->m6b) HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4519 ttaaggaACTGCTGa CAGCAGUG m7a Created HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4660 ttaagGAGCTGCtga UGCAGCUC m7b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-497-5p ttaaggaGCTGCTGa CAGCAGCA m7a Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-584-3p ttaaGGAACTGctga UCAGUUCC m7b Created HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-646 ttaaggAGCTGCTga AAGCAGCU m7b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-6736-3p ttaaGGAGCTGctga UCAGCUCC m7b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-424-5p ttaaggaGCTGCTGa CAGCAGCA m7a Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4274 ttaaggaACTGCTGa CAGCAGUC m7a Created HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4448 ttAAGGAGCtgctga GGCUCCUU m7b (m7b->m6b) HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4519 ttaaggaACTGCTGa CAGCAGUG m7a Created HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4660 ttaagGAGCTGCtga UGCAGCUC m7b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-497-5p ttaaggaGCTGCTGa CAGCAGCA m7a Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-584-3p ttaaGGAACTGctga UCAGUUCC m7b Created HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-646 ttaaggAGCTGCTga AAGCAGCU m7b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-6736-3p ttaaGGAGCTGctga UCAGCUCC m7b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-424-5p ttaaggaGCTGCTGa CAGCAGCA m7a Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4274 ttaaggaACTGCTGa CAGCAGUC m7a Created HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4448 ttAAGGAGCtgctga GGCUCCUU m7b (m7b->m6b) HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4519 ttaaggaACTGCTGa CAGCAGUG m7a Created HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4660 ttaagGAGCTGCtga UGCAGCUC m7b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-497-5p ttaaggaGCTGCTGa CAGCAGCA m7a Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090653G>T COSM4734840 T3499 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-214-3p aggagCTGCTGagca ACAGCAGG m6b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-3928-5p agGAGCTTCtgagca UGAAGCUC m7b (m6b->m7b) HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-424-5p aggaGCTGCTGagca CAGCAGCA m7a Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4291 aggagCTGCTGAgca UUCAGCAG m7b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4660 agGAGCTGCtgagca UGCAGCUC m7b (m7b->m6b) HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-497-5p aggaGCTGCTGagca CAGCAGCA m7a Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-646 aggAGCTGCTgagca AAGCAGCU m7b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-6736-3p aGGAGCTGctgagca UCAGCUCC m7b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-6806-3p agGAGCTTCtgagca UGAAGCUC m7b (m6b->m7b) HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-761 aggagCTGCTGagca GCAGCAGG m6b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-922 aggagCTGCTGagca GCAGCAGA m6b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-214-3p aggagCTGCTGagca ACAGCAGG m6b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-3928-5p agGAGCTTCtgagca UGAAGCUC m7b (m6b->m7b) HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-424-5p aggaGCTGCTGagca CAGCAGCA m7a Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4291 aggagCTGCTGAgca UUCAGCAG m7b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4660 agGAGCTGCtgagca UGCAGCUC m7b (m7b->m6b) HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-497-5p aggaGCTGCTGagca CAGCAGCA m7a Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-646 aggAGCTGCTgagca AAGCAGCU m7b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-6736-3p aGGAGCTGctgagca UCAGCUCC m7b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-6806-3p agGAGCTTCtgagca UGAAGCUC m7b (m6b->m7b) HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-761 aggagCTGCTGagca GCAGCAGG m6b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-922 aggagCTGCTGagca GCAGCAGA m6b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-214-3p aggagCTGCTGagca ACAGCAGG m6b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-3928-5p agGAGCTTCtgagca UGAAGCUC m7b (m6b->m7b) HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-424-5p aggaGCTGCTGagca CAGCAGCA m7a Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4291 aggagCTGCTGAgca UUCAGCAG m7b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-4660 agGAGCTGCtgagca UGCAGCUC m7b (m7b->m6b) HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-497-5p aggaGCTGCTGagca CAGCAGCA m7a Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-646 aggAGCTGCTgagca AAGCAGCU m7b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-6736-3p aGGAGCTGctgagca UCAGCUCC m7b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-6806-3p agGAGCTTCtgagca UGAAGCUC m7b (m6b->m7b) HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-761 aggagCTGCTGagca GCAGCAGG m6b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-922 aggagCTGCTGagca GCAGCAGA m6b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-214-3p aggagCTGCTGagca ACAGCAGG m6b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-3928-5p agGAGCTTCtgagca UGAAGCUC m7b (m6b->m7b) HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-424-5p aggaGCTGCTGagca CAGCAGCA m7a Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4291 aggagCTGCTGAgca UUCAGCAG m7b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-4660 agGAGCTGCtgagca UGCAGCUC m7b (m7b->m6b) HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-497-5p aggaGCTGCTGagca CAGCAGCA m7a Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-646 aggAGCTGCTgagca AAGCAGCU m7b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-6736-3p aGGAGCTGctgagca UCAGCUCC m7b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-6806-3p agGAGCTTCtgagca UGAAGCUC m7b (m6b->m7b) HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-761 aggagCTGCTGagca GCAGCAGG m6b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-922 aggagCTGCTGagca GCAGCAGA m6b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090649A>T COSM1496982 TCGA-CJ-4869-01 [kidney][NS][carcinoma][clear_cell_renal_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3130-3p gctgctGTGCAGact GCUGCACC m6b Created HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-6828-3p gctgctGAGCAGAct AUCUGCUC m7b Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-767-3p gctgcTGAGCAGAct UCUGCUCA m8a Disrupted HHHNA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-3130-3p gctgctGTGCAGact GCUGCACC m6b Created HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-6828-3p gctgctGAGCAGAct AUCUGCUC m7b Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-767-3p gctgcTGAGCAGAct UCUGCUCA m8a Disrupted HHHNE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-3130-3p gctgctGTGCAGact GCUGCACC m6b Created HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-6828-3p gctgctGAGCAGAct AUCUGCUC m7b Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-767-3p gctgcTGAGCAGAct UCUGCUCA m8a Disrupted HHHSA_22279_TNC|NM_002160|exon_CDS|-7.77652423762806|-1.28231555011894
hsa-miR-3130-3p gctgctGTGCAGact GCUGCACC m6b Created HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-6828-3p gctgctGAGCAGAct AUCUGCUC m7b Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704
hsa-miR-767-3p gctgcTGAGCAGAct UCUGCUCA m8a Disrupted HHHSE_19284_TNC|NM_002160|exon_CDS|-8.04477855170355|0.106319498935704

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090592G>T COSM3903461 TCGA-BR-8487-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1184 taCTGCAGGagcagg CCUGCAGC m7a (m7a->m6a) HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-17-3p tACTGCAGgagcagg ACUGCAGU m7b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-1976 tactGCAGGAGcagg CCUCCUGC m7b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-3158-5p taCTGCAGGagcagg CCUGCAGA m7a (m7a->m6a) HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4268 tactgcAGGAGCagg GGCUCCUC m6b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4448 tactgcAGGAGCagg GGCUCCUU m6b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-6772-3p tactgcAGGAGCAgg UUGCUCCU m7b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-6847-3p tactgCATGAGCagg GGCUCAUG m7b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-767-3p tactgcaTGAGCAGg UCUGCUCA m7b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-1184 taCTGCAGGagcagg CCUGCAGC m7a (m7a->m6a) HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-17-3p tACTGCAGgagcagg ACUGCAGU m7b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-1976 tactGCAGGAGcagg CCUCCUGC m7b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-3158-5p taCTGCAGGagcagg CCUGCAGA m7a (m7a->m6a) HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4268 tactgcAGGAGCagg GGCUCCUC m6b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4448 tactgcAGGAGCagg GGCUCCUU m6b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-6772-3p tactgcAGGAGCAgg UUGCUCCU m7b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-6847-3p tactgCATGAGCagg GGCUCAUG m7b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-767-3p tactgcaTGAGCAGg UCUGCUCA m7b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090582G>T COSM1288525 NB-1599 [autonomic_ganglia][NS][neuroblastoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-596 GCAGGCTTctgtctc AAGCCUGC m8a Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-596 GCAGGCTTctgtctc AAGCCUGC m8a Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090568G>A COSM1554129 TCGA-55-6987-01 [lung][right_lower_lobe][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4536-5p ccagcCTACCACAgg UGUGGUAG m8a Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4736 ccagCCTGCCacagg AGGCAGGU m6b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4763-3p ccagCCTGCCacagg AGGCAGGG m6b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-7150 ccagCCTGCCAcagg CUGGCAGG m7b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-891a-3p ccagccTGCCACagg AGUGGCAC m6b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-3688-5p ccagccTGCCACagg AGUGGCAA m6b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4536-5p ccagcCTACCACAgg UGUGGUAG m8a Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4736 ccagCCTGCCacagg AGGCAGGU m6b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4763-3p ccagCCTGCCacagg AGGCAGGG m6b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-7150 ccagCCTGCCAcagg CUGGCAGG m7b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-891a-3p ccagccTGCCACagg AGUGGCAC m6b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-3688-5p ccagccTGCCACagg AGUGGCAA m6b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090566C>T COSM1554130 TCGA-44-7661-01 [lung][right_lower_lobe][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3137 agcctGCTACAGgta UCUGUAGC m7b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-3688-5p agccTGCCACaggta AGUGGCAA m6b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4690-5p aGCCTGCTacaggta GAGCAGGC m7b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-6165 agCCTGCTacaggta CAGCAGGA m6b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-6510-5p agCCTGCTacaggta CAGCAGGG m6b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-7150 agCCTGCCAcaggta CUGGCAGG m7b (m7b->m6b) HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-891a-3p agccTGCCACaggta AGUGGCAC m6b Disrupted HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-3137 agcctGCTACAGgta UCUGUAGC m7b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-3688-5p agccTGCCACaggta AGUGGCAA m6b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-4690-5p aGCCTGCTacaggta GAGCAGGC m7b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-6165 agCCTGCTacaggta CAGCAGGA m6b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-6510-5p agCCTGCTacaggta CAGCAGGG m6b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-7150 agCCTGCCAcaggta CUGGCAGG m7b (m7b->m6b) HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-891a-3p agccTGCCACaggta AGUGGCAC m6b Disrupted HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090563A>G COSM3903460 TCGA-CD-A4MG-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-100-5p ctgccACGGGTatga AACCCGUA m6b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-132-5p ctGCCACGGgtatga ACCGUGGC m7b (m6b->m7b) HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-99a-5p ctgccACGGGTatga AACCCGUA m6b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-99b-5p ctgccACGGGTatga CACCCGUA m6b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-100-5p ctgccACGGGTatga AACCCGUA m6b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-132-5p ctGCCACGGgtatga ACCGUGGC m7b (m6b->m7b) HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-99a-5p ctgccACGGGTatga AACCCGUA m6b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-99b-5p ctgccACGGGTatga CACCCGUA m6b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115090562G>C COSM4548829 CSCC-41-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-644a tGCCACACgtatgag AGUGUGGC m7b Created HHHNA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109
hsa-miR-644a tGCCACACgtatgag AGUGUGGC m7b Created HHHSA_22278_TNC|NM_002160|exon_CDS|-7.98357704656974|0.511504457426109

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087260C>A COSM4628816 Gp2D [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2861 tggacacCAGGCCCt GGGGCCUG m7b Disrupted HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-3657 tGGACACAaggccct UGUGUCCC m7a Created HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-4312 tggacACAAGGCCct GGCCUUGU m8a Created HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-4669 tGGACACAaggccct UGUGUCCG m7a Created HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-581 tggACACAAGgccct UCUUGUGU m7b Created HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-599 tgGACACAAggccct GUUGUGUC m7b (m6b->m7b) HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-7978 tggACACCAGgccct UCUGGUGU m7b Disrupted HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-2861 tggacacCAGGCCCt GGGGCCUG m7b Disrupted HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-3657 tGGACACAaggccct UGUGUCCC m7a Created HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-4312 tggacACAAGGCCct GGCCUUGU m8a Created HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-4669 tGGACACAaggccct UGUGUCCG m7a Created HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-581 tggACACAAGgccct UCUUGUGU m7b Created HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-599 tgGACACAAggccct GUUGUGUC m7b (m6b->m7b) HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-7978 tggACACCAGgccct UCUGGUGU m7b Disrupted HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087241C>T COSM1104466 TCGA-B5-A0JY-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3189-5p tagcggtTGGGGCAa UGCCCCAU m7a Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4758-3p tagcggtTGGGGCAa UGCCCCAC m7a Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-5699-5p tagcggTTGGGGCAa UGCCCCAA m8a Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-6793-3p tagcgGTTGGGGcaa UCCCCAAC m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3189-5p tagcggtTGGGGCAa UGCCCCAU m7a Created HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-4758-3p tagcggtTGGGGCAa UGCCCCAC m7a Created HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-5699-5p tagcggTTGGGGCAa UGCCCCAA m8a Created HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-6793-3p tagcgGTTGGGGcaa UCCCCAAC m7b Created HHHNE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-3189-5p tagcggtTGGGGCAa UGCCCCAU m7a Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4758-3p tagcggtTGGGGCAa UGCCCCAC m7a Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-5699-5p tagcggTTGGGGCAa UGCCCCAA m8a Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-6793-3p tagcgGTTGGGGcaa UCCCCAAC m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3189-5p tagcggtTGGGGCAa UGCCCCAU m7a Created HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-4758-3p tagcggtTGGGGCAa UGCCCCAC m7a Created HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-5699-5p tagcggTTGGGGCAa UGCCCCAA m8a Created HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528
hsa-miR-6793-3p tagcgGTTGGGGcaa UCCCCAAC m7b Created HHHSE_19283_TNC|NM_002160|exon_CDS|-8.70218640832615|0.886005654560528

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087211T>G COSM1104465 TCGA-BS-A0UJ-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-449b-3p aTGTGGCTGtgtctg CAGCCACA m8a (m8a->m7a) HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4691-3p atGTGGCTGtgtctg CCAGCCAC m7b (m7b->m6b) HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-449b-3p aTGTGGCTGtgtctg CAGCCACA m8a (m8a->m7a) HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4691-3p atGTGGCTGtgtctg CCAGCCAC m7b (m7b->m6b) HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087209T>G COSM1236171 MM1S [haematopoietic_and_lymphoid_tissue][NS][lymphoid_neoplasm][plasma_cell_myeloma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3166 gtggctgTGTCTGCg CGCAGACA m7b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4691-3p GTGGCTGGgtctgcg CCAGCCAC m8a Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3166 gtggctgTGTCTGCg CGCAGACA m7b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4691-3p GTGGCTGGgtctgcg CCAGCCAC m8a Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087203C>T COSM287994 TCGA-HT-7688-01 [central_nervous_system][brain][glioma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3166 gTGTCTGCGaacctg CGCAGACA m8a (m8a->m7a) HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-6767-5p gtGTCTGCGAacctg UCGCAGAC m8a Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3166 gTGTCTGCGaacctg CGCAGACA m8a (m8a->m7a) HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-6767-5p gtGTCTGCGAacctg UCGCAGAC m8a Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087202G>A COSM3926041 TCGA-FW-A3R5-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4464 tgtctgCAAACCTgg AAGGUUUG m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4748 tgtctgCAAACCTgg GAGGUUUG m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-6767-5p tGTCTGCGAacctgg UCGCAGAC m8a (m8a->m7a) HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-1273h-3p tGTCTGCAaacctgg CUGCAGAC m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4464 tgtctgCAAACCTgg AAGGUUUG m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4748 tgtctgCAAACCTgg GAGGUUUG m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-6767-5p tGTCTGCGAacctgg UCGCAGAC m8a (m8a->m7a) HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087170G>A COSM4734839 T2944 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4437 gctcTGAGCCCgaat UGGGCUCA m7b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4750-5p gctctgaGCCCGAat CUCGGGCG m6b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-125b-1-3p gctctgAACCCGaat ACGGGUUA m6b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-24-3p gctCTGAGCCcgaat UGGCUCAG m7b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3181 gctctgaGCCCGAat AUCGGGCC m6b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3944-3p gctctgAGCCCGAAt UUCGGGCU m8a Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4437 gctcTGAGCCCgaat UGGGCUCA m7b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4750-5p gctctgaGCCCGAat CUCGGGCG m6b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-125b-1-3p gctctgAACCCGaat ACGGGUUA m6b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-24-3p gctCTGAGCCcgaat UGGCUCAG m7b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3181 gctctgaGCCCGAat AUCGGGCC m6b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3944-3p gctctgAGCCCGAAt UUCGGGCU m8a Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4437 gctcTGAGCCCgaat UGGGCUCA m7b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4750-5p gctctgaGCCCGAat CUCGGGCG m6b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-125b-1-3p gctctgAACCCGaat ACGGGUUA m6b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-24-3p gctCTGAGCCcgaat UGGCUCAG m7b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3181 gctctgaGCCCGAat AUCGGGCC m6b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3944-3p gctctgAGCCCGAAt UUCGGGCU m8a Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4437 gctcTGAGCCCgaat UGGGCUCA m7b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4750-5p gctctgaGCCCGAat CUCGGGCG m6b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-125b-1-3p gctctgAACCCGaat ACGGGUUA m6b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-24-3p gctCTGAGCCcgaat UGGCUCAG m7b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3181 gctctgaGCCCGAat AUCGGGCC m6b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3944-3p gctctgAGCCCGAAt UUCGGGCU m8a Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4437 gctcTGAGCCCgaat UGGGCUCA m7b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4750-5p gctctgaGCCCGAat CUCGGGCG m6b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-125b-1-3p gctctgAACCCGaat ACGGGUUA m6b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-24-3p gctCTGAGCCcgaat UGGCUCAG m7b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3181 gctctgaGCCCGAat AUCGGGCC m6b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3944-3p gctctgAGCCCGAAt UUCGGGCU m8a Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4437 gctcTGAGCCCgaat UGGGCUCA m7b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4750-5p gctctgaGCCCGAat CUCGGGCG m6b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-125b-1-3p gctctgAACCCGaat ACGGGUUA m6b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-24-3p gctCTGAGCCcgaat UGGCUCAG m7b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3181 gctctgaGCCCGAat AUCGGGCC m6b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3944-3p gctctgAGCCCGAAt UUCGGGCU m8a Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087167C>T COSM201994 TCGA-A6-2672-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-181a-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-181b-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-181c-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-181d-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3155a ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3155b ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3181 ctgaGCCCGAatgtc AUCGGGCC m6b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3944-3p ctgAGCCCGAAtgtc UUCGGGCU m8a Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4262 ctgagccTGAATGTc GACAUUCA m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4437 cTGAGCCCgaatgtc UGGGCUCA m7b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4750-5p ctgaGCCCGAatgtc CUCGGGCG m6b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-484 ctGAGCCTGAatgtc UCAGGCUC m8a Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-506-5p ctgagCCTGAATgtc UAUUCAGG m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-181a-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-181b-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-181c-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-181d-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3155a ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3155b ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3181 ctgaGCCCGAatgtc AUCGGGCC m6b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3944-3p ctgAGCCCGAAtgtc UUCGGGCU m8a Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4262 ctgagccTGAATGTc GACAUUCA m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4437 cTGAGCCCgaatgtc UGGGCUCA m7b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4750-5p ctgaGCCCGAatgtc CUCGGGCG m6b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-484 ctGAGCCTGAatgtc UCAGGCUC m8a Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-506-5p ctgagCCTGAATgtc UAUUCAGG m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-181a-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-181b-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-181c-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-181d-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3155a ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3155b ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3181 ctgaGCCCGAatgtc AUCGGGCC m6b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3944-3p ctgAGCCCGAAtgtc UUCGGGCU m8a Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4262 ctgagccTGAATGTc GACAUUCA m7b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4437 cTGAGCCCgaatgtc UGGGCUCA m7b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4750-5p ctgaGCCCGAatgtc CUCGGGCG m6b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-484 ctGAGCCTGAatgtc UCAGGCUC m8a Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-506-5p ctgagCCTGAATgtc UAUUCAGG m7b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-181a-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-181b-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-181c-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-181d-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3155a ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3155b ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3181 ctgaGCCCGAatgtc AUCGGGCC m6b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3944-3p ctgAGCCCGAAtgtc UUCGGGCU m8a Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4262 ctgagccTGAATGTc GACAUUCA m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4437 cTGAGCCCgaatgtc UGGGCUCA m7b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4750-5p ctgaGCCCGAatgtc CUCGGGCG m6b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-484 ctGAGCCTGAatgtc UCAGGCUC m8a Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-506-5p ctgagCCTGAATgtc UAUUCAGG m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-181a-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-181b-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-181c-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-181d-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3155a ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3155b ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3181 ctgaGCCCGAatgtc AUCGGGCC m6b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3944-3p ctgAGCCCGAAtgtc UUCGGGCU m8a Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4262 ctgagccTGAATGTc GACAUUCA m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4437 cTGAGCCCgaatgtc UGGGCUCA m7b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4750-5p ctgaGCCCGAatgtc CUCGGGCG m6b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-484 ctGAGCCTGAatgtc UCAGGCUC m8a Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-506-5p ctgagCCTGAATgtc UAUUCAGG m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-181a-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-181b-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-181c-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-181d-5p ctgagccTGAATGTc AACAUUCA m7b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3155a ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3155b ctGAGCCTGaatgtc CCAGGCUC m7b (m6b->m7b) HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3181 ctgaGCCCGAatgtc AUCGGGCC m6b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3944-3p ctgAGCCCGAAtgtc UUCGGGCU m8a Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4262 ctgagccTGAATGTc GACAUUCA m7b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4437 cTGAGCCCgaatgtc UGGGCUCA m7b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4750-5p ctgaGCCCGAatgtc CUCGGGCG m6b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-484 ctGAGCCTGAatgtc UCAGGCUC m8a Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-506-5p ctgagCCTGAATgtc UAUUCAGG m7b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087166G>A COSM288254 TCGA-AG-3726-01 [large_intestine][rectum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1587 tgAGCCCAAatgtcc UUGGGCUG m7a (m6a->m7a) HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3181 tgaGCCCGAatgtcc AUCGGGCC m6b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3620-5p tgAGCCCAaatgtcc GUGGGCUG m6b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3944-3p tgAGCCCGAAtgtcc UUCGGGCU m8a Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4437 TGAGCCCAaatgtcc UGGGCUCA m8a Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4674 tGAGCCCAaatgtcc CUGGGCUC m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4750-5p tgaGCCCGAatgtcc CUCGGGCG m6b Disrupted HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-1587 tgAGCCCAAatgtcc UUGGGCUG m7a (m6a->m7a) HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3181 tgaGCCCGAatgtcc AUCGGGCC m6b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3620-5p tgAGCCCAaatgtcc GUGGGCUG m6b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3944-3p tgAGCCCGAAtgtcc UUCGGGCU m8a Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4437 TGAGCCCAaatgtcc UGGGCUCA m8a Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4674 tGAGCCCAaatgtcc CUGGGCUC m7b Created HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4750-5p tgaGCCCGAatgtcc CUCGGGCG m6b Disrupted HHHNA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-1587 tgAGCCCAAatgtcc UUGGGCUG m7a (m6a->m7a) HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3181 tgaGCCCGAatgtcc AUCGGGCC m6b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3620-5p tgAGCCCAaatgtcc GUGGGCUG m6b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3944-3p tgAGCCCGAAtgtcc UUCGGGCU m8a Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4437 TGAGCCCAaatgtcc UGGGCUCA m8a Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4674 tGAGCCCAaatgtcc CUGGGCUC m7b Created HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4750-5p tgaGCCCGAatgtcc CUCGGGCG m6b Disrupted HHHNE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-1587 tgAGCCCAAatgtcc UUGGGCUG m7a (m6a->m7a) HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3181 tgaGCCCGAatgtcc AUCGGGCC m6b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3620-5p tgAGCCCAaatgtcc GUGGGCUG m6b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-3944-3p tgAGCCCGAAtgtcc UUCGGGCU m8a Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4437 TGAGCCCAaatgtcc UGGGCUCA m8a Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4674 tGAGCCCAaatgtcc CUGGGCUC m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4750-5p tgaGCCCGAatgtcc CUCGGGCG m6b Disrupted HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-1587 tgAGCCCAAatgtcc UUGGGCUG m7a (m6a->m7a) HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3181 tgaGCCCGAatgtcc AUCGGGCC m6b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3620-5p tgAGCCCAaatgtcc GUGGGCUG m6b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-3944-3p tgAGCCCGAAtgtcc UUCGGGCU m8a Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4437 TGAGCCCAaatgtcc UGGGCUCA m8a Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4674 tGAGCCCAaatgtcc CUGGGCUC m7b Created HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-4750-5p tgaGCCCGAatgtcc CUCGGGCG m6b Disrupted HHHSA_22277_TNC|NM_002160|exon_CDS|-7.33421473579754|0.326465495166006
hsa-miR-1587 tgAGCCCAAatgtcc UUGGGCUG m7a (m6a->m7a) HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3181 tgaGCCCGAatgtcc AUCGGGCC m6b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3620-5p tgAGCCCAaatgtcc GUGGGCUG m6b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-3944-3p tgAGCCCGAAtgtcc UUCGGGCU m8a Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4437 TGAGCCCAaatgtcc UGGGCUCA m8a Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4674 tGAGCCCAaatgtcc CUGGGCUC m7b Created HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602
hsa-miR-4750-5p tgaGCCCGAatgtcc CUCGGGCG m6b Disrupted HHHSE_19282_TNC|NM_002160|exon_CDS|-8.20643091779798|-1.58875394317602

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087142C>T COSM277742 YULAN [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-548m tcACCTTTGaggccg CAAAGGUA m7a (m6a->m7a) HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-548m tcACCTTTGaggccg CAAAGGUA m7a (m6a->m7a) HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087141G>A COSM3321507 T2950 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4635 cacCTTCAAGgccgg UCUUGAAG m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-493-3p cACCTTCAaggccgg UGAAGGUC m7a Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-6126 caCCTTCAaggccgg GUGAAGGC m6b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4635 cacCTTCAAGgccgg UCUUGAAG m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-493-3p cACCTTCAaggccgg UGAAGGUC m7a Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-6126 caCCTTCAaggccgg GUGAAGGC m6b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087104C>T COSM3903459 TCGA-BR-4188-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4786-3p gtgacgaTGGCTTCa UGAAGCCA m7b Created HHHNA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4786-3p gtgacgaTGGCTTCa UGAAGCCA m7b Created HHHNE_19280_TNC|NM_002160|exon_CDS|-8.31563418114246|0.467397895850381
hsa-miR-4786-3p gtgacgaTGGCTTCa UGAAGCCA m7b Created HHHSA_22276_TNC|NM_002160|exon_CDS|-7.27032638876576|-1.05492097779247
hsa-miR-4786-3p gtgacgaTGGCTTCa UGAAGCCA m7b Created HHHSE_19280_TNC|NM_002160|exon_CDS|-8.31563418114246|0.467397895850381

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087096C>T COSM751903 PARBRK [haematopoietic_and_lymphoid_tissue][NS][lymphoid_neoplasm][acute_lymphoblastic_B_cell_leukaemia]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4641 ggcttCATGGGCgag UGCCCAUG m7b Created HHHNE_19280_TNC|NM_002160|exon_CDS|-8.31563418114246|0.467397895850381
hsa-miR-8060 ggCTTCATGGgcgag CCAUGAAG m8a Created HHHNE_19280_TNC|NM_002160|exon_CDS|-8.31563418114246|0.467397895850381
hsa-miR-4641 ggcttCATGGGCgag UGCCCAUG m7b Created HHHSE_19280_TNC|NM_002160|exon_CDS|-8.31563418114246|0.467397895850381
hsa-miR-8060 ggCTTCATGGgcgag CCAUGAAG m8a Created HHHSE_19280_TNC|NM_002160|exon_CDS|-8.31563418114246|0.467397895850381
Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087035A>G COSM3763576 TCGA-AM-5820-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087014C>T COSM1104464 CSCC-49-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1323 tctGTTTTGAaggct UCAAAACU m7a Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-548o-3p tctGTTTTGaaggct CCAAAACU m6b Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-1323 tctGTTTTGAaggct UCAAAACU m7a Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-548o-3p tctGTTTTGaaggct CCAAAACU m6b Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115087013G>A COSM3653438 TCGA-EB-A5UN-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3614-3p ctgtttcGAAGGCTa UAGCCUUC m7b Disrupted HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-494-3p cTGTTTCAaaggcta UGAAACAU m7a Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-510-3p ctGTTTCAAaggcta AUUGAAAC m7b (m6b->m7b) HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-5581-5p ctgtttcGAAGGCTa AGCCUUCC m7a Disrupted HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-3614-3p ctgtttcGAAGGCTa UAGCCUUC m7b Disrupted HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-494-3p cTGTTTCAaaggcta UGAAACAU m7a Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-510-3p ctGTTTCAAaggcta AUUGAAAC m7b (m6b->m7b) HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-5581-5p ctgtttcGAAGGCTa AGCCUUCC m7a Disrupted HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086985G>A COSM4588398 CHEWS004 [bone][NS][Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-647 tGCAGCCAtgaaatc GUGGCUGC m7b Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-889-5p tgCAGCCATgaaatc AAUGGCUG m7b (m6b->m7b) HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-647 tGCAGCCAtgaaatc GUGGCUGC m7b Created HHHNE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-889-5p tgCAGCCATgaaatc AAUGGCUG m7b (m6b->m7b) HHHNE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-647 tGCAGCCAtgaaatc GUGGCUGC m7b Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-889-5p tgCAGCCATgaaatc AAUGGCUG m7b (m6b->m7b) HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-647 tGCAGCCAtgaaatc GUGGCUGC m7b Created HHHSE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-889-5p tgCAGCCATgaaatc AAUGGCUG m7b (m6b->m7b) HHHSE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086971G>T COSM1194067 H358 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1285-3p cTGCCCAGtgccctg UCUGGGCA m7b Disrupted HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-3187-5p cTGCCCAGtgccctg CCUGGGCA m7b Disrupted HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-5189-5p cTGCCCAGtgccctg UCUGGGCA m7b Disrupted HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-612 cTGCCCAGtgccctg GCUGGGCA m7b Disrupted HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-6860 cTGCCCAGTgccctg ACUGGGCA m8a (m8a->m7a) HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-1285-3p cTGCCCAGtgccctg UCUGGGCA m7b Disrupted HHHNE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-3187-5p cTGCCCAGtgccctg CCUGGGCA m7b Disrupted HHHNE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-5189-5p cTGCCCAGtgccctg UCUGGGCA m7b Disrupted HHHNE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-612 cTGCCCAGtgccctg GCUGGGCA m7b Disrupted HHHNE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-6860 cTGCCCAGTgccctg ACUGGGCA m8a (m8a->m7a) HHHNE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-1285-3p cTGCCCAGtgccctg UCUGGGCA m7b Disrupted HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-3187-5p cTGCCCAGtgccctg CCUGGGCA m7b Disrupted HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-5189-5p cTGCCCAGtgccctg UCUGGGCA m7b Disrupted HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-612 cTGCCCAGtgccctg GCUGGGCA m7b Disrupted HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-6860 cTGCCCAGTgccctg ACUGGGCA m8a (m8a->m7a) HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-1285-3p cTGCCCAGtgccctg UCUGGGCA m7b Disrupted HHHSE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-3187-5p cTGCCCAGtgccctg CCUGGGCA m7b Disrupted HHHSE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-5189-5p cTGCCCAGtgccctg UCUGGGCA m7b Disrupted HHHSE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-612 cTGCCCAGtgccctg GCUGGGCA m7b Disrupted HHHSE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223
hsa-miR-6860 cTGCCCAGTgccctg ACUGGGCA m8a (m8a->m7a) HHHSE_19279_TNC|NM_002160|exon_CDS|-8.96014659156959|-1.00607834200223

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086952A>G COSM4798994 BCM325T [liver][NS][carcinoma][hepatocellular_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3648 gaggagCGCGGCaca AGCCGCGG m6b Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-6772-3p gAGGAGCAcggcaca UUGCUCCU m7b Disrupted HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-6869-3p gaggaGCGCGGCaca CGCCGCGC m7b Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-3648 gaggagCGCGGCaca AGCCGCGG m6b Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-6772-3p gAGGAGCAcggcaca UUGCUCCU m7b Disrupted HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-6869-3p gaggaGCGCGGCaca CGCCGCGC m7b Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086951C>T COSM201993 TCGA-AA-3710-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1227-3p aggagcaTGGCACat CGUGCCAC m6b Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-4659a-5p aggagCATGGCAcat CUGCCAUG m7b Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-4659b-5p aggagCATGGCAcat UUGCCAUG m7b Created HHHNA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-1227-3p aggagcaTGGCACat CGUGCCAC m6b Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-4659a-5p aggagCATGGCAcat CUGCCAUG m7b Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321
hsa-miR-4659b-5p aggagCATGGCAcat UUGCCAUG m7b Created HHHSA_22275_TNC|NM_002160|exon_CDS|-7.84332051611088|1.21894919517321

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086922G>A COSM607205 TCGA-35-4122-01 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-150-3p tgtgTGTACCAcgat CUGGUACA m7b Created HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-8485 TGTGTGTGccacgat CACACACA m8a Disrupted HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-891a-3p tgtgtGTGCCACgat AGUGGCAC m7b Disrupted HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-150-3p tgtgTGTACCAcgat CUGGUACA m7b Created HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-8485 TGTGTGTGccacgat CACACACA m8a Disrupted HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-891a-3p tgtgtGTGCCACgat AGUGGCAC m7b Disrupted HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086921C>T COSM3903457 TCGA-D7-A4YV-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-642a-3p gtgTGTGTCacgatg AGACACAU m6b Created HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-642b-3p gtgTGTGTCacgatg AGACACAU m6b Created HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-891a-3p gtgtGTGCCACgatg AGUGGCAC m7b Disrupted HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-642a-3p gtgTGTGTCacgatg AGACACAU m6b Created HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-642b-3p gtgTGTGTCacgatg AGACACAU m6b Created HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-891a-3p gtgtGTGCCACgatg AGUGGCAC m7b Disrupted HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086902G>A COSM201992 TCGA-AA-3864-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4317 tgcaGGCAATGactg ACAUUGCC m7b Created HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-4763-5p tGCAGGCGatgactg CGCCUGCC m7a Disrupted HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-616-3p tgcaggCAATGACTg AGUCAUUG m8a Created HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-6785-3p tgcaGGCGATGactg ACAUCGCC m7b Disrupted HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-6894-3p tGCAGGCAAtgactg UUGCCUGC m8a (m7a->m8a) HHHNA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-4317 tgcaGGCAATGactg ACAUUGCC m7b Created HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-4763-5p tGCAGGCGatgactg CGCCUGCC m7a Disrupted HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-616-3p tgcaggCAATGACTg AGUCAUUG m8a Created HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-6785-3p tgcaGGCGATGactg ACAUCGCC m7b Disrupted HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796
hsa-miR-6894-3p tGCAGGCAAtgactg UUGCCUGC m8a (m7a->m8a) HHHSA_22274_TNC|NM_002160|exon_CDS|-7.88732137733122|0.269971707123796

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086865A>C COSM1559847 TCGA-06-0122-01 [central_nervous_system][brain][glioma][astrocytoma_Grade_IV]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4766-3p aATTGCTAcaaccgt AUAGCAAU m7b Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6081 aatTGCTCCaaccgt AGGAGCAG m6b Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6874-5p aattGCTCCAaccgt AUGGAGCU m6b Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-4766-3p aATTGCTAcaaccgt AUAGCAAU m7b Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6081 aatTGCTCCaaccgt AGGAGCAG m6b Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6874-5p aattGCTCCAaccgt AUGGAGCU m6b Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086854C>T COSM3784193 TCGA-EJ-7782-01 [prostate][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086853G>A COSM1229857 587342 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3912-5p cgTGGACAatgcgtg AUGUCCAU m6b Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-3912-5p cgTGGACAatgcgtg AUGUCCAU m6b Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086841A>G COSM165027 PD4100a [breast][NS][carcinoma][ductal_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6758-3p gtggaGAATGAGTgc ACUCAUUC m8a Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6794-3p gtggAGAGTGAGtgc CUCACUCU m8a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-3680-5p gtggagAGTGAGTgc GACUCACU m7b Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-4639-3p gtgGAGAGTGAgtgc UCACUCUC m8a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6758-3p gtggaGAATGAGTgc ACUCAUUC m8a Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6794-3p gtggAGAGTGAGtgc CUCACUCU m8a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-3680-5p gtggagAGTGAGTgc GACUCACU m7b Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-4639-3p gtgGAGAGTGAgtgc UCACUCUC m8a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086840T>C COSM3382404 PCSI_0083_Pa_P [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6758-3p tggaGAATGAGTgcg ACUCAUUC m8a Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6758-3p tggaGAATGAGTgcg ACUCAUUC m8a Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086834C>T COSM3903456 TCGA-F1-6177-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-521 atgAGTGCGTgtgtg AACGCACU m7b Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-603 atgAGTGTGTGtgtg CACACACU m8a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-8485 atgagTGTGTGTGtg CACACACA m8a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-521 atgAGTGCGTgtgtg AACGCACU m7b Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-603 atgAGTGTGTGtgtg CACACACU m8a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-8485 atgagTGTGTGTGtg CACACACA m8a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086809G>A COSM1104463 TCGA-AX-A0J0-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6726-3p cacGGGCGAagactg CUCGCCCU m6b Disrupted HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-6726-3p cacGGGCGAagactg CUCGCCCU m6b Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6726-3p cacGGGCGAagactg CUCGCCCU m6b Disrupted HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-6726-3p cacGGGCGAagactg CUCGCCCU m6b Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086799G>C COSM353622 LUAD_E00522 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1304-3p gactgCAGTGAGctc UCUCACUG m7b Disrupted HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-130a-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-130b-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-143-5p gACTGCACtgagctc GGUGCAGU m7b Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-148a-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-148b-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-152-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-17-3p gACTGCAGTgagctc ACUGCAGU m8a (m8a->m7a) HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-301a-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-301b-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-3666 gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-4295 gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-4418 gaCTGCAGTGagctc CACUGCAG m8a Disrupted HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-509-3-5p gaCTGCAGTgagctc UACUGCAG m7b (m7b->m6b) HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-509-5p gaCTGCAGTgagctc UACUGCAG m7b (m7b->m6b) HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-6807-3p gacTGCAGTGagctc CACUGCAU m7a Disrupted HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-6854-5p gactgcaCTGAGCTc AAGCUCAG m7b Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-6890-3p gactGCAGTGagctc CCACUGCC m6b Disrupted HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-1304-3p gactgCAGTGAGctc UCUCACUG m7b Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-130a-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-130b-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-143-5p gACTGCACtgagctc GGUGCAGU m7b Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-148a-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-148b-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-152-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-17-3p gACTGCAGTgagctc ACUGCAGU m8a (m8a->m7a) HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-301a-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-301b-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-3666 gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-4295 gacTGCACTGagctc CAGUGCAA m7a Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-4418 gaCTGCAGTGagctc CACUGCAG m8a Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-509-3-5p gaCTGCAGTgagctc UACUGCAG m7b (m7b->m6b) HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-509-5p gaCTGCAGTgagctc UACUGCAG m7b (m7b->m6b) HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6807-3p gacTGCAGTGagctc CACUGCAU m7a Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6854-5p gactgcaCTGAGCTc AAGCUCAG m7b Created HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6890-3p gactGCAGTGagctc CCACUGCC m6b Disrupted HHHNA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-1304-3p gactgCAGTGAGctc UCUCACUG m7b Disrupted HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-130a-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-130b-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-143-5p gACTGCACtgagctc GGUGCAGU m7b Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-148a-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-148b-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-152-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-17-3p gACTGCAGTgagctc ACUGCAGU m8a (m8a->m7a) HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-301a-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-301b-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-3666 gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-4295 gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-4418 gaCTGCAGTGagctc CACUGCAG m8a Disrupted HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-509-3-5p gaCTGCAGTgagctc UACUGCAG m7b (m7b->m6b) HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-509-5p gaCTGCAGTgagctc UACUGCAG m7b (m7b->m6b) HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-6807-3p gacTGCAGTGagctc CACUGCAU m7a Disrupted HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-6854-5p gactgcaCTGAGCTc AAGCUCAG m7b Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-6890-3p gactGCAGTGagctc CCACUGCC m6b Disrupted HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-1304-3p gactgCAGTGAGctc UCUCACUG m7b Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-130a-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-130b-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-143-5p gACTGCACtgagctc GGUGCAGU m7b Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-148a-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-148b-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-152-3p gacTGCACTGAgctc UCAGUGCA m8a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-17-3p gACTGCAGTgagctc ACUGCAGU m8a (m8a->m7a) HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-301a-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-301b-3p gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-3666 gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-4295 gacTGCACTGagctc CAGUGCAA m7a Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-4418 gaCTGCAGTGagctc CACUGCAG m8a Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-509-3-5p gaCTGCAGTgagctc UACUGCAG m7b (m7b->m6b) HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-509-5p gaCTGCAGTgagctc UACUGCAG m7b (m7b->m6b) HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6807-3p gacTGCAGTGagctc CACUGCAU m7a Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6854-5p gactgcaCTGAGCTc AAGCUCAG m7b Created HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224
hsa-miR-6890-3p gactGCAGTGagctc CCACUGCC m6b Disrupted HHHSA_22273_TNC|NM_002160|exon_CDS|-7.64586332963902|2.63064884725224

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086767C>T COSM218973 ICGC_0019 [pancreas][NS][carcinoma][ductal_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-874-5p cttcgacTGGGGCCg CGGCCCCA m7b Created HHHNA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-874-5p cttcgacTGGGGCCg CGGCCCCA m7b Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-874-5p cttcgacTGGGGCCg CGGCCCCA m7b Created HHHSA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-874-5p cttcgacTGGGGCCg CGGCCCCA m7b Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086762C>T COSM3903455 TCGA-HU-A4GU-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4670-5p accggGGTCGCTgca AAGCGACC m7b Created HHHNA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-4670-5p accggGGTCGCTgca AAGCGACC m7b Created HHHNA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675
hsa-miR-4670-5p accggGGTCGCTgca AAGCGACC m7b Created HHHSA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-4670-5p accggGGTCGCTgca AAGCGACC m7b Created HHHSA_22272_TNC|NM_002160|exon_CDS|-7.27488544801335|1.59183253699675

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086740T>G COSM421979 TCGA-BL-A0C8-01 [urinary_tract][bladder][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4690-5p caCCTGCTactgcga GAGCAGGC m6b Disrupted HHHSA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-6165 caCCTGCTactgcga CAGCAGGA m6b Disrupted HHHSA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-6510-5p caCCTGCTactgcga CAGCAGGG m6b Disrupted HHHSA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-4690-5p caCCTGCTactgcga GAGCAGGC m6b Disrupted HHHNA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-6165 caCCTGCTactgcga CAGCAGGA m6b Disrupted HHHNA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-6510-5p caCCTGCTactgcga CAGCAGGG m6b Disrupted HHHNA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086734G>A COSM1701578 YUKLAB [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4778-3p ctactgcGAAGAAGg UCUUCUUC m7b Disrupted HHHNA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-6516-5p ctACTGCAAAgaagg UUUGCAGU m8a Created HHHNA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-4778-3p ctactgcGAAGAAGg UCUUCUUC m7b Disrupted HHHSA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682
hsa-miR-6516-5p ctACTGCAAAgaagg UUUGCAGU m8a Created HHHSA_22271_TNC|NM_002160|exon_CDS|-7.11634039657073|1.15889072707682

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086678C>T COSM3847466 TCGA-EW-A423-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3688-5p ccTGCCACacccagg AGUGGCAA m6b Disrupted HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-4455 cctgcCACACCCagg AGGGUGUG m7b Disrupted HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-503-3p cctgccATACCCagg GGGGUAUU m6b Created HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-609 cctgccACACCCagg AGGGUGUU m6b Disrupted HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-644a cctGCCACACccagg AGUGUGGC m7b Disrupted HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-6776-5p cctgccaCACCCAGg UCUGGGUG m7b Disrupted HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-6861-5p cctgccaTACCCAGg ACUGGGUA m7b Created HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-891a-3p ccTGCCACacccagg AGUGGCAC m6b Disrupted HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-3688-5p ccTGCCACacccagg AGUGGCAA m6b Disrupted HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-4455 cctgcCACACCCagg AGGGUGUG m7b Disrupted HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-503-3p cctgccATACCCagg GGGGUAUU m6b Created HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-609 cctgccACACCCagg AGGGUGUU m6b Disrupted HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-644a cctGCCACACccagg AGUGUGGC m7b Disrupted HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-6776-5p cctgccaCACCCAGg UCUGGGUG m7b Disrupted HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-6861-5p cctgccaTACCCAGg ACUGGGUA m7b Created HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-891a-3p ccTGCCACacccagg AGUGGCAC m6b Disrupted HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086669C>T COSM3653437 TCGA-ER-A194-01 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1291 ccCAGGGCCggtgtg UGGCCCUG m7b (m7b->m6b) HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-4725-5p ccCAGGGTCggtgtg AGACCCUG m7b (m6b->m7b) HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-504-5p ccCAGGGTCggtgtg AGACCCUG m7b (m6b->m7b) HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-6775-3p ccCAGGGCCggtgtg AGGCCCUG m7b (m7b->m6b) HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-1291 ccCAGGGCCggtgtg UGGCCCUG m7b (m7b->m6b) HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-4725-5p ccCAGGGTCggtgtg AGACCCUG m7b (m6b->m7b) HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-504-5p ccCAGGGTCggtgtg AGACCCUG m7b (m6b->m7b) HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-6775-3p ccCAGGGCCggtgtg AGGCCCUG m7b (m7b->m6b) HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086668C>T COSM3321496 08-P8005 [bone][NS][Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1226-3p ccaggGCTGGTGtga UCACCAGC m7b Created HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-6775-3p cCAGGGCCggtgtga AGGCCCUG m7b Disrupted HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-1226-3p ccaggGCTGGTGtga UCACCAGC m7b Created HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-6775-3p cCAGGGCCggtgtga AGGCCCUG m7b Disrupted HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086666G>A COSM4734837 T3225 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-342-3p agggccgGTGTGAGg UCUCACAC m7b Disrupted HHHNE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
hsa-miR-342-3p agggccgGTGTGAGg UCUCACAC m7b Disrupted HHHSE_19278_TNC|NM_002160|exon_CDS|-8.09075387790653|-0.347555100803458
Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086628C>T COSM3653436 TCGA-EE-A29B-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086626G>A COSM3926040 TCGA-ER-A3EV-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3128 ctTTGCCAGtgtgga UCUGGCAA m7b (m6b->m7b) HHHNE_19276_TNC|NM_002160|exon_CDS|-8.42527515041273|-0.122567558676331
hsa-miR-6757-3p ctttgCCAGTGTgga AACACUGG m7b Created HHHNE_19276_TNC|NM_002160|exon_CDS|-8.42527515041273|-0.122567558676331
hsa-miR-3128 ctTTGCCAGtgtgga UCUGGCAA m7b (m6b->m7b) HHHNH_3939_TNC|NM_002160|exon_CDS|-9.04998123115572|0.183615908735132
hsa-miR-6757-3p ctttgCCAGTGTgga AACACUGG m7b Created HHHNH_3939_TNC|NM_002160|exon_CDS|-9.04998123115572|0.183615908735132
hsa-miR-3128 ctTTGCCAGtgtgga UCUGGCAA m7b (m6b->m7b) HHHSE_19276_TNC|NM_002160|exon_CDS|-8.42527515041273|-0.122567558676331
hsa-miR-6757-3p ctttgCCAGTGTgga AACACUGG m7b Created HHHSE_19276_TNC|NM_002160|exon_CDS|-8.42527515041273|-0.122567558676331
hsa-miR-3128 ctTTGCCAGtgtgga UCUGGCAA m7b (m6b->m7b) HHHSH_3939_TNC|NM_002160|exon_CDS|-9.04998123115572|0.183615908735132
hsa-miR-6757-3p ctttgCCAGTGTgga AACACUGG m7b Created HHHSH_3939_TNC|NM_002160|exon_CDS|-9.04998123115572|0.183615908735132

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086554G>T COSM1496983 TCGA-B0-5098-01 [kidney][NS][carcinoma][clear_cell_renal_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-21-3p gcGGTGTTagtgtga CAACACCA m6b Created HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-342-3p gcgGTGTGAGtgtga UCUCACAC m7b Disrupted HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-3591-3p gcGGTGTTagtgtga AAACACCA m6b Created HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-21-3p gcGGTGTTagtgtga CAACACCA m6b Created HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-342-3p gcgGTGTGAGtgtga UCUCACAC m7b Disrupted HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-3591-3p gcGGTGTTagtgtga AAACACCA m6b Created HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086552G>T COSM4856528 TCGA-C5-A7UE-01 [cervix][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-216b-3p ggtgtgAGTGTGatg ACACACUU m6b Disrupted HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-4705 ggtGTGATTGtgatg UCAAUCAC m7b Created HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-216b-3p ggtgtgAGTGTGatg ACACACUU m6b Disrupted HHHSE_19275_TNC|NM_002160|exon_CDS|-8.35083343131379|-0.0131152487263174
hsa-miR-4705 ggtGTGATTGtgatg UCAAUCAC m7b Created HHHSE_19275_TNC|NM_002160|exon_CDS|-8.35083343131379|-0.0131152487263174
hsa-miR-216b-3p ggtgtgAGTGTGatg ACACACUU m6b Disrupted HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-4705 ggtGTGATTGtgatg UCAAUCAC m7b Created HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-216b-3p ggtgtgAGTGTGatg ACACACUU m6b Disrupted HHHNE_19275_TNC|NM_002160|exon_CDS|-8.35083343131379|-0.0131152487263174
hsa-miR-4705 ggtGTGATTGtgatg UCAAUCAC m7b Created HHHNE_19275_TNC|NM_002160|exon_CDS|-8.35083343131379|-0.0131152487263174

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086499G>A COSM1104461 TCGA-AP-A0LM-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1184 cccaatgGCTGCAGt CCUGCAGC m7b Disrupted HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-17-3p cccaatgACTGCAGt ACUGCAGU m7b Created HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-616-3p ccCAATGACTgcagt AGUCAUUG m8a Created HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-7156-3p cccaatGGCTGCAGt CUGCAGCC m8a Disrupted HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-1184 cccaatgGCTGCAGt CCUGCAGC m7b Disrupted HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-17-3p cccaatgACTGCAGt ACUGCAGU m7b Created HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-616-3p ccCAATGACTgcagt AGUCAUUG m8a Created HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-7156-3p cccaatGGCTGCAGt CUGCAGCC m8a Disrupted HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-1184 cccaatgGCTGCAGt CCUGCAGC m7b Disrupted HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-17-3p cccaatgACTGCAGt ACUGCAGU m7b Created HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-616-3p ccCAATGACTgcagt AGUCAUUG m8a Created HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-7156-3p cccaatGGCTGCAGt CUGCAGCC m8a Disrupted HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-1184 cccaatgGCTGCAGt CCUGCAGC m7b Disrupted HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-17-3p cccaatgACTGCAGt ACUGCAGU m7b Created HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-616-3p ccCAATGACTgcagt AGUCAUUG m8a Created HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-7156-3p cccaatGGCTGCAGt CUGCAGCC m8a Disrupted HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086489C>T COSM1459587 TCGA-AZ-6598-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4252 gCAGTGGCCatggcc GGCCACUG m8a (m8a->m7a) HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-4701-5p gcaGTGGCCAtggcc UUGGCCAC m7b Disrupted HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-588 gcaGTGGCCAtggcc UUGGCCAC m7b Disrupted HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-1273g-3p GCAGTGGTcatggcc ACCACUGC m8a Created HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-4252 gCAGTGGCCatggcc GGCCACUG m8a (m8a->m7a) HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-4701-5p gcaGTGGCCAtggcc UUGGCCAC m7b Disrupted HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-588 gcaGTGGCCAtggcc UUGGCCAC m7b Disrupted HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-1273g-3p GCAGTGGTcatggcc ACCACUGC m8a Created HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-4252 gCAGTGGCCatggcc GGCCACUG m8a (m8a->m7a) HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-4701-5p gcaGTGGCCAtggcc UUGGCCAC m7b Disrupted HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-588 gcaGTGGCCAtggcc UUGGCCAC m7b Disrupted HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-1273g-3p GCAGTGGTcatggcc ACCACUGC m8a Created HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-4252 gCAGTGGCCatggcc GGCCACUG m8a (m8a->m7a) HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-4701-5p gcaGTGGCCAtggcc UUGGCCAC m7b Disrupted HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-588 gcaGTGGCCAtggcc UUGGCCAC m7b Disrupted HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086482C>G COSM3653435 TCGA-EE-A3J5-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6746-3p ccatGGCGGCTGtgt CAGCCGCC m8a Created HHHNA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-6746-3p ccatGGCGGCTGtgt CAGCCGCC m8a Created HHHNE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158
hsa-miR-6746-3p ccatGGCGGCTGtgt CAGCCGCC m8a Created HHHSA_22270_TNC|NM_002160|exon_CDS|-7.70552446602159|-0.354936458956949
hsa-miR-6746-3p ccatGGCGGCTGtgt CAGCCGCC m8a Created HHHSE_19274_TNC|NM_002160|exon_CDS|-7.58536916892715|-0.905434448154158

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086459G>A COSM1158819 8014777 [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-377-3p agtgtgTGTGTGATg AUCACACA m8a Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-3941 aGTGTGTAtgtgatg UUACACAC m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-603 AGTGTGTGtgtgatg CACACACU m8a Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-8485 agtgTGTGTGTGatg CACACACA m8a Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-377-3p agtgtgTGTGTGATg AUCACACA m8a Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-3941 aGTGTGTAtgtgatg UUACACAC m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-603 AGTGTGTGtgtgatg CACACACU m8a Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-8485 agtgTGTGTGTGatg CACACACA m8a Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086454A>TGA COSM1459586 TCGA-AY-6197-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-377-3p gTGTGTGATgagggc AUCACACA m8a (m8a->m7a) HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6072 gtgtgtGATGAGGgc UCCUCAUC m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6891-3p gtgtgtGATGAGGGc CCCUCAUC m8a Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-8485 gTGTGTGTGatgagggc CACACACA m8a (m7a->m8a) HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-377-3p gTGTGTGATgagggc AUCACACA m8a (m8a->m7a) HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6072 gtgtgtGATGAGGgc UCCUCAUC m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6891-3p gtgtgtGATGAGGGc CCCUCAUC m8a Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-8485 gTGTGTGTGatgagggc CACACACA m8a (m7a->m8a) HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086452G>A COSM455235 TCGA-B6-A0IK-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-129-1-3p gtgtgatAAGGGCTa AAGCCCUU m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-129-2-3p gtgtgatAAGGGCTa AAGCCCUU m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4687-5p gtgtgatGAGGGCTa CAGCCCUC m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6072 gtgtGATGAGGgcta UCCUCAUC m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6891-3p gtgtGATGAGGGcta CCCUCAUC m8a Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-938 gtgtgaTAAGGGCta UGCCCUUA m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-129-1-3p gtgtgatAAGGGCTa AAGCCCUU m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-129-2-3p gtgtgatAAGGGCTa AAGCCCUU m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4687-5p gtgtgatGAGGGCTa CAGCCCUC m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6072 gtgtGATGAGGgcta UCCUCAUC m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6891-3p gtgtGATGAGGGcta CCCUCAUC m8a Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-938 gtgtgaTAAGGGCta UGCCCUUA m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086451A>C COSM3903453 TCGA-HJ-7597-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-129-1-3p tgtgatgAGGGCTat AAGCCCUU m6b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-129-2-3p tgtgatgAGGGCTat AAGCCCUU m6b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-3940-3p tgtgatgCGGGCTat CAGCCCGG m6b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4687-5p tgtgatGAGGGCTat CAGCCCUC m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4707-3p tgtgatGCGGGCTat AGCCCGCC m7a Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6072 tgtGATGAGGgctat UCCUCAUC m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6779-3p tgtgatgAGGGCTat AAGCCCUG m6b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6891-3p tgtGATGAGGGctat CCCUCAUC m8a Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-7112-3p tGTGATGCgggctat UGCAUCAC m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-129-1-3p tgtgatgAGGGCTat AAGCCCUU m6b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-129-2-3p tgtgatgAGGGCTat AAGCCCUU m6b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-3940-3p tgtgatgCGGGCTat CAGCCCGG m6b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4687-5p tgtgatGAGGGCTat CAGCCCUC m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4707-3p tgtgatGCGGGCTat AGCCCGCC m7a Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6072 tgtGATGAGGgctat UCCUCAUC m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6779-3p tgtgatgAGGGCTat AAGCCCUG m6b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6891-3p tgtGATGAGGGctat CCCUCAUC m8a Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-7112-3p tGTGATGCgggctat UGCAUCAC m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086433A>G COSM751904 TCGA-66-2758-01 [lung][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-455-3p ggggaGGACTGCagc GCAGUCCA m7a Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-4687-5p gggGAGGGCTGcagc CAGCCCUC m8a Created HHFCT_158262_cluster-23497_16_8
hsa-miR-4690-3p ggggaGGGCTGCagc GCAGCCCA m7a Created HHFCT_158262_cluster-23497_16_8
hsa-miR-6749-3p gGGGAGGActgcagc CUCCUCCC m7b Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-7156-3p ggggagGGCTGCAGc CUGCAGCC m8a Created HHFCT_158262_cluster-23497_16_8
hsa-miR-1184 ggggaggGCTGCAGc CCUGCAGC m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-17-3p ggggaggACTGCAGc ACUGCAGU m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-1910-5p ggggAGGACTGcagc CCAGUCCU m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4290 ggGGAGGGCtgcagc UGCCCUCC m7b (m6b->m7b) HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-455-3p ggggaGGACTGCagc GCAGUCCA m7a Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4687-5p gggGAGGGCTGcagc CAGCCCUC m8a Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4690-3p ggggaGGGCTGCagc GCAGCCCA m7a Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6749-3p gGGGAGGActgcagc CUCCUCCC m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-7156-3p ggggagGGCTGCAGc CUGCAGCC m8a Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-1184 ggggaggGCTGCAGc CCUGCAGC m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-17-3p ggggaggACTGCAGc ACUGCAGU m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-1910-5p ggggAGGACTGcagc CCAGUCCU m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4290 ggGGAGGGCtgcagc UGCCCUCC m7b (m6b->m7b) HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-455-3p ggggaGGACTGCagc GCAGUCCA m7a Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4687-5p gggGAGGGCTGcagc CAGCCCUC m8a Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4690-3p ggggaGGGCTGCagc GCAGCCCA m7a Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6749-3p gGGGAGGActgcagc CUCCUCCC m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-7156-3p ggggagGGCTGCAGc CUGCAGCC m8a Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-1184 ggggaggGCTGCAGc CCUGCAGC m7b Created HHFCT_158262_cluster-23497_16_8
hsa-miR-17-3p ggggaggACTGCAGc ACUGCAGU m7b Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-1910-5p ggggAGGACTGcagc CCAGUCCU m7b Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-4290 ggGGAGGGCtgcagc UGCCCUCC m7b (m6b->m7b) HHFCT_158262_cluster-23497_16_8

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086428A>C COSM4760522 pfg034T [stomach][NS][carcinoma][mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-17-3p ggACTGCAGccagct ACUGCAGU m7b (m7b->m6b) HHFCT_158262_cluster-23497_16_8
hsa-miR-3064-5p ggactgCAGCCAGct UCUGGCUG m7b Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-5580-5p ggactgcAGCCAGCt UGCUGGCU m7b Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-604 ggactGCAGCCagct AGGCUGCG m6b Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-647 ggactGCAGCCAgct GUGGCUGC m7b Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-6504-5p ggactgCAGCCAGct UCUGGCUG m7b Disrupted HHFCT_158262_cluster-23497_16_8
hsa-miR-6770-3p ggactGCCGCCAGct CUGGCGGC m8a Created HHFCT_158262_cluster-23497_16_8
hsa-miR-6820-5p ggaCTGCCGCcagct UGCGGCAG m7b Created HHFCT_158262_cluster-23497_16_8
hsa-miR-17-3p ggACTGCAGccagct ACUGCAGU m7b (m7b->m6b) HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-3064-5p ggactgCAGCCAGct UCUGGCUG m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-5580-5p ggactgcAGCCAGCt UGCUGGCU m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-604 ggactGCAGCCagct AGGCUGCG m6b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-647 ggactGCAGCCAgct GUGGCUGC m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6504-5p ggactgCAGCCAGct UCUGGCUG m7b Disrupted HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6770-3p ggactGCCGCCAGct CUGGCGGC m8a Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6820-5p ggaCTGCCGCcagct UGCGGCAG m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-17-3p ggACTGCAGccagct ACUGCAGU m7b (m7b->m6b) HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-3064-5p ggactgCAGCCAGct UCUGGCUG m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-5580-5p ggactgcAGCCAGCt UGCUGGCU m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-604 ggactGCAGCCagct AGGCUGCG m6b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-647 ggactGCAGCCAgct GUGGCUGC m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6504-5p ggactgCAGCCAGct UCUGGCUG m7b Disrupted HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6770-3p ggactGCCGCCAGct CUGGCGGC m8a Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6820-5p ggaCTGCCGCcagct UGCGGCAG m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086419C>T COSM1459585 TCGA-AA-3492-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-593-5p ccagctaTGGTGCCc AGGCACCA m7b Created HHFCT_158262_cluster-23497_16_8
hsa-miR-767-5p ccagctATGGTGCcc UGCACCAU m7b Created HHFCT_158262_cluster-23497_16_8
hsa-miR-593-5p ccagctaTGGTGCCc AGGCACCA m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-767-5p ccagctATGGTGCcc UGCACCAU m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-593-5p ccagctaTGGTGCCc AGGCACCA m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-767-5p ccagctATGGTGCcc UGCACCAU m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086418G>A COSM1739539 M020 [haematopoietic_and_lymphoid_tissue][NS][lymphoid_neoplasm][mantle_cell_lymphoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1183 cagCTACAGTGcccc CACUGUAG m8a Created HHFCT_158262_cluster-23497_16_8
hsa-miR-3137 caGCTACAGtgcccc UCUGUAGC m7b (m6b->m7b) HHFCT_158262_cluster-23497_16_8
hsa-miR-1183 cagCTACAGTGcccc CACUGUAG m8a Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-3137 caGCTACAGtgcccc UCUGUAGC m7b (m6b->m7b) HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-1183 cagCTACAGTGcccc CACUGUAG m8a Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-3137 caGCTACAGtgcccc UCUGUAGC m7b (m6b->m7b) HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086394G>A COSM241954 WA16 [prostate][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1291 cacagtCAGGGCCgc UGGCCCUG m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4732-3p cacaGTCAGGGCcgc GCCCUGAC m8a Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6775-3p cacagtCAGGGCCgc AGGCCCUG m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-7976 cacagTCAGGGCcgc UGCCCUGA m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-943 cACAGTCAGggccgc CUGACUGU m8a (m7a->m8a) HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-1291 cacagtCAGGGCCgc UGGCCCUG m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4732-3p cacaGTCAGGGCcgc GCCCUGAC m8a Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6775-3p cacagtCAGGGCCgc AGGCCCUG m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-7976 cacagTCAGGGCcgc UGCCCUGA m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-943 cACAGTCAGggccgc CUGACUGU m8a (m7a->m8a) HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086389C>T COSM1559846 TCGA-06-0122-01 [central_nervous_system][brain][glioma][astrocytoma_Grade_IV]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086389C>G COSM328254 Capan-1 [pancreas][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4632-3p tcgGGGCGGCtgtgt UGCCGCCC m7b Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6746-3p tcggGGCGGCTGtgt CAGCCGCC m8a Created HHHNA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-4632-3p tcgGGGCGGCtgtgt UGCCGCCC m7b Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232
hsa-miR-6746-3p tcggGGCGGCTGtgt CAGCCGCC m8a Created HHHSA_22269_TNC|NM_002160|exon_CDS|-6.78940763283906|0.376462901408232

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086310G>A COSM3952246 J90_T [lung][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4645-3p aatgACTGTCaccag AGACAGUA m6b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-542-3p aatgaCTGTCACcag UGUGACAG m7b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-4645-3p aatgACTGTCaccag AGACAGUA m6b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-542-3p aatgaCTGTCACcag UGUGACAG m7b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086299G>A COSM3367524 TCGA-CJ-4889-01 [kidney][NS][carcinoma][clear_cell_renal_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1199-3p ccagcaCGGCCGCtg UGCGGCCG m7b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-5008-3p ccAGCACAGccgctg CCUGUGCU m7b (m6b->m7b) HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6737-3p ccAGCACAGccgctg UCUGUGCU m7b (m6b->m7b) HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-7157-3p ccAGCACAGccgctg UCUGUGCU m7b (m6b->m7b) HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-7974 ccagCACAGCCgctg AGGCUGUG m7b Created HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-1199-3p ccagcaCGGCCGCtg UGCGGCCG m7b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-5008-3p ccAGCACAGccgctg CCUGUGCU m7b (m6b->m7b) HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6737-3p ccAGCACAGccgctg UCUGUGCU m7b (m6b->m7b) HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-7157-3p ccAGCACAGccgctg UCUGUGCU m7b (m6b->m7b) HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-7974 ccagCACAGCCgctg AGGCUGUG m7b Created HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086296C>T COSM3929763 TCGA-QH-A65V-01 [central_nervous_system][brain][glioma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1199-3p gcaCGGCCGCtgtgt UGCGGCCG m7b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-1199-3p gcaCGGCCGCtgtgt UGCGGCCG m7b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086254G>T COSM3903452 TCGA-BR-8361-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-331-3p ctacaCAGGGGaaga GCCCCUGG m6b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-3679-3p ctacacaGGGGAAGa CUUCCCCC m7a Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-511-3p cTACACATgggaaga AAUGUGUA m7b Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6801-3p ctacaCAGGGGaaga ACCCCUGC m6b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6810-3p ctacaCAGGGGAaga UCCCCUGC m7a Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6826-3p ctacacAGGGGAaga CUCCCCUC m6b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-331-3p ctacaCAGGGGaaga GCCCCUGG m6b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-3679-3p ctacacaGGGGAAGa CUUCCCCC m7a Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-511-3p cTACACATgggaaga AAUGUGUA m7b Created HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6801-3p ctacaCAGGGGaaga ACCCCUGC m6b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6810-3p ctacaCAGGGGAaga UCCCCUGC m7a Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6826-3p ctacacAGGGGAaga CUCCCCUC m6b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-331-3p ctacaCAGGGGaaga GCCCCUGG m6b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-3679-3p ctacacaGGGGAAGa CUUCCCCC m7a Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-511-3p cTACACATgggaaga AAUGUGUA m7b Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6801-3p ctacaCAGGGGaaga ACCCCUGC m6b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6810-3p ctacaCAGGGGAaga UCCCCUGC m7a Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6826-3p ctacacAGGGGAaga CUCCCCUC m6b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-331-3p ctacaCAGGGGaaga GCCCCUGG m6b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-3679-3p ctacacaGGGGAAGa CUUCCCCC m7a Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-511-3p cTACACATgggaaga AAUGUGUA m7b Created HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6801-3p ctacaCAGGGGaaga ACCCCUGC m6b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6810-3p ctacaCAGGGGAaga UCCCCUGC m7a Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6826-3p ctacacAGGGGAaga CUCCCCUC m6b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086252G>A COSM3653434 TCGA-GN-A266-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1976 acaCAGGAGaagact CCUCCUGC m6b Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-331-3p acaCAGGGGaagact GCCCCUGG m6b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-3653-5p acaCAGGAGaagact CCUCCUGA m6b Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-3679-3p acacaGGGGAAGact CUUCCCCC m7a Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-4279 acacAGGAGAagact CUCUCCUC m6b Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6740-3p acacaggAGAAGACt UGUCUUCU m7b Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6801-3p acaCAGGGGaagact ACCCCUGC m6b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6810-3p acaCAGGGGAagact UCCCCUGC m7a Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6826-3p acacAGGGGAagact CUCCCCUC m6b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-1976 acaCAGGAGaagact CCUCCUGC m6b Created HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-331-3p acaCAGGGGaagact GCCCCUGG m6b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-3653-5p acaCAGGAGaagact CCUCCUGA m6b Created HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-3679-3p acacaGGGGAAGact CUUCCCCC m7a Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-4279 acacAGGAGAagact CUCUCCUC m6b Created HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6740-3p acacaggAGAAGACt UGUCUUCU m7b Created HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6801-3p acaCAGGGGaagact ACCCCUGC m6b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6810-3p acaCAGGGGAagact UCCCCUGC m7a Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6826-3p acacAGGGGAagact CUCCCCUC m6b Disrupted HHHNA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-1976 acaCAGGAGaagact CCUCCUGC m6b Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-331-3p acaCAGGGGaagact GCCCCUGG m6b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-3653-5p acaCAGGAGaagact CCUCCUGA m6b Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-3679-3p acacaGGGGAAGact CUUCCCCC m7a Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-4279 acacAGGAGAagact CUCUCCUC m6b Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6740-3p acacaggAGAAGACt UGUCUUCU m7b Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6801-3p acaCAGGGGaagact ACCCCUGC m6b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6810-3p acaCAGGGGAagact UCCCCUGC m7a Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6826-3p acacAGGGGAagact CUCCCCUC m6b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-1976 acaCAGGAGaagact CCUCCUGC m6b Created HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-331-3p acaCAGGGGaagact GCCCCUGG m6b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-3653-5p acaCAGGAGaagact CCUCCUGA m6b Created HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-3679-3p acacaGGGGAAGact CUUCCCCC m7a Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-4279 acacAGGAGAagact CUCUCCUC m6b Created HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6740-3p acacaggAGAAGACt UGUCUUCU m7b Created HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6801-3p acaCAGGGGaagact ACCCCUGC m6b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6810-3p acaCAGGGGAagact UCCCCUGC m7a Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
hsa-miR-6826-3p acacAGGGGAagact CUCCCCUC m6b Disrupted HHHSA_22268_TNC|NM_002160|exon_CDS|-7.30354165589597|-1.45232236285406
Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086243C>T COSM4734836 T3064 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086242C>T COSM3903451 TCGA-BR-8363-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4274 aGACTGCTGggatcg CAGCAGUC m8a (m7a->m8a) HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-4530 agaCTGCTGGGatcg CCCAGCAG m8a Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-7977 agactGCTGGGAtcg UUCCCAGC m7b Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-4274 aGACTGCTGggatcg CAGCAGUC m8a (m7a->m8a) HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-4530 agaCTGCTGGGatcg CCCAGCAG m8a Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-7977 agactGCTGGGAtcg UUCCCAGC m7b Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086236C>T COSM4734835 T578 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-182-5p ccgggaTTGCCAAtg UUUGGCAA m7b Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6717-5p ccgggATCGCCaatg AGGCGAUG m6b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-8053 ccgggATCGCCAatg UGGCGAUU m7a Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-182-5p ccgggaTTGCCAAtg UUUGGCAA m7b Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6717-5p ccgggATCGCCaatg AGGCGAUG m6b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-8053 ccgggATCGCCAatg UGGCGAUU m7a Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086235G>A COSM35457 TCGA-02-0010-01 [central_nervous_system][brain][glioma][astrocytoma_Grade_IV]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6717-5p cgggATCGCCaatgc AGGCGAUG m6b Disrupted HHHNA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-8053 cgggATCGCCAatgc UGGCGAUU m7a Disrupted HHHNA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-6717-5p cgggATCGCCaatgc AGGCGAUG m6b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-8053 cgggATCGCCAatgc UGGCGAUU m7a Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-6717-5p cgggATCGCCaatgc AGGCGAUG m6b Disrupted HHHSA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-8053 cgggATCGCCAatgc UGGCGAUU m7a Disrupted HHHSA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-6717-5p cgggATCGCCaatgc AGGCGAUG m6b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-8053 cgggATCGCCAatgc UGGCGAUU m7a Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086232A>G COSM4940444 TCGA-DD-A11A-01 [liver][NS][carcinoma][hepatocellular_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4285 gaTCGCCGatgcccc GCGGCGAG m6b Created HHHNA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-8053 gATCGCCAatgcccc UGGCGAUU m7a Disrupted HHHNA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-1256 gatcgcCAATGCCcc AGGCAUUG m7b Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-4285 gaTCGCCGatgcccc GCGGCGAG m6b Created HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-8053 gATCGCCAatgcccc UGGCGAUU m7a Disrupted HHHNA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-1256 gatcgcCAATGCCcc AGGCAUUG m7b Disrupted HHHSA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-4285 gaTCGCCGatgcccc GCGGCGAG m6b Created HHHSA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-8053 gATCGCCAatgcccc UGGCGAUU m7a Disrupted HHHSA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657
hsa-miR-1256 gatcgcCAATGCCcc AGGCAUUG m7b Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-4285 gaTCGCCGatgcccc GCGGCGAG m6b Created HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-8053 gATCGCCAatgcccc UGGCGAUU m7a Disrupted HHHSA_22267_TNC|NM_002160|exon_CDS|-7.86979708613242|-0.319811502381157
hsa-miR-1256 gatcgcCAATGCCcc AGGCAUUG m7b Disrupted HHHNA_22266_TNC|NM_002160|exon_CDS|-8.15430507625848|0.901266732312657

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086161G>A COSM1624472 TCGA-BR-A4CS-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-138-5p cttCACCAGCcctga AGCUGGUG m7b Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-3918 cttcaccGGCCCTGa ACAGGGCC m7b Disrupted HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4299 ctTCACCAGCcctga GCUGGUGA m8a Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4446-3p cttcacCAGCCCTGa CAGGGCUG m8a Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4492 cttcaCCAGCCCtga GGGGCUGG m7b Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4498 cttcaCCAGCCCtga UGGGCUGG m7b Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4512 cttcaccGGCCCTGa CAGGGCCU m7a Disrupted HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-5001-5p cttcaCCAGCCCTga AGGGCUGG m8a Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-5088-5p cttcaccAGCCCTGa CAGGGCUC m7a Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-6781-5p cttcaCCGGCCCtga CGGGCCGG m7b Disrupted HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-6895-5p cttcaccGGCCCTGa CAGGGCCA m7a Disrupted HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-7160-3p cttcaccGGCCCTGa CAGGGCCC m7a Disrupted HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-762 cttcaCCAGCCCtga GGGGCUGG m7b Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-138-5p cttCACCAGCcctga AGCUGGUG m7b Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-3918 cttcaccGGCCCTGa ACAGGGCC m7b Disrupted HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4299 ctTCACCAGCcctga GCUGGUGA m8a Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4446-3p cttcacCAGCCCTGa CAGGGCUG m8a Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4492 cttcaCCAGCCCtga GGGGCUGG m7b Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4498 cttcaCCAGCCCtga UGGGCUGG m7b Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4512 cttcaccGGCCCTGa CAGGGCCU m7a Disrupted HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-5001-5p cttcaCCAGCCCTga AGGGCUGG m8a Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-5088-5p cttcaccAGCCCTGa CAGGGCUC m7a Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-6781-5p cttcaCCGGCCCtga CGGGCCGG m7b Disrupted HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-6895-5p cttcaccGGCCCTGa CAGGGCCA m7a Disrupted HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-7160-3p cttcaccGGCCCTGa CAGGGCCC m7a Disrupted HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-762 cttcaCCAGCCCtga GGGGCUGG m7b Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086156T>G COSM3699363 TCGA-G4-6320-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3127-5p ccgGCCCTGActgtg AUCAGGGC m7b Disrupted HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-3918 ccGGCCCTGactgtg ACAGGGCC m7b (m7b->m6b) HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4512 ccGGCCCTGactgtg CAGGGCCU m7a (m7a->m6a) HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-6781-5p CCGGCCCGgactgtg CGGGCCGG m8a Created HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-6895-5p ccGGCCCTGactgtg CAGGGCCA m7a (m7a->m6a) HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-7160-3p ccGGCCCTGactgtg CAGGGCCC m7a (m7a->m6a) HHHNE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-3127-5p ccgGCCCTGActgtg AUCAGGGC m7b Disrupted HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-3918 ccGGCCCTGactgtg ACAGGGCC m7b (m7b->m6b) HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-4512 ccGGCCCTGactgtg CAGGGCCU m7a (m7a->m6a) HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-6781-5p CCGGCCCGgactgtg CGGGCCGG m8a Created HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-6895-5p ccGGCCCTGactgtg CAGGGCCA m7a (m7a->m6a) HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934
hsa-miR-7160-3p ccGGCCCTGactgtg CAGGGCCC m7a (m7a->m6a) HHHSE_19273_TNC|NM_002160|exon_CDS|-8.53401104599103|-1.85834943315934

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086110C>T COSM201991 TCGA-AA-3977-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3120-3p ccagggTTGCTGTGt CACAGCAA m8a Created HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-4670-5p ccagGGTCGCTgtgt AAGCGACC m7b Disrupted HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-4725-5p cCAGGGTCgctgtgt AGACCCUG m7b Disrupted HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-504-5p cCAGGGTCgctgtgt AGACCCUG m7b Disrupted HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-6732-3p cCAGGGTTgctgtgt UAACCCUG m7b Created HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-3120-3p ccagggTTGCTGTGt CACAGCAA m8a Created HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-4670-5p ccagGGTCGCTgtgt AAGCGACC m7b Disrupted HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-4725-5p cCAGGGTCgctgtgt AGACCCUG m7b Disrupted HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-504-5p cCAGGGTCgctgtgt AGACCCUG m7b Disrupted HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-6732-3p cCAGGGTTgctgtgt UAACCCUG m7b Created HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-3120-3p ccagggTTGCTGTGt CACAGCAA m8a Created HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-4670-5p ccagGGTCGCTgtgt AAGCGACC m7b Disrupted HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-4725-5p cCAGGGTCgctgtgt AGACCCUG m7b Disrupted HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-504-5p cCAGGGTCgctgtgt AGACCCUG m7b Disrupted HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-6732-3p cCAGGGTTgctgtgt UAACCCUG m7b Created HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-3120-3p ccagggTTGCTGTGt CACAGCAA m8a Created HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-4670-5p ccagGGTCGCTgtgt AAGCGACC m7b Disrupted HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-4725-5p cCAGGGTCgctgtgt AGACCCUG m7b Disrupted HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-504-5p cCAGGGTCgctgtgt AGACCCUG m7b Disrupted HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-6732-3p cCAGGGTTgctgtgt UAACCCUG m7b Created HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086098G>A COSM3653433 TCGA-ER-A2ND-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086090C>T COSM1459583 TCGA-AD-6964-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-106b-3p ggCAGTGCGtgtgcc CCGCACUG m7b (m7b->m6b) HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-521 ggcAGTGCGTgtgcc AACGCACU m7b Disrupted HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-603 ggcAGTGTGTGtgcc CACACACU m8a Created HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-8485 ggcagTGTGTGTGcc CACACACA m8a Created HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-106b-3p ggCAGTGCGtgtgcc CCGCACUG m7b (m7b->m6b) HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-521 ggcAGTGCGTgtgcc AACGCACU m7b Disrupted HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-603 ggcAGTGTGTGtgcc CACACACU m8a Created HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-8485 ggcagTGTGTGTGcc CACACACA m8a Created HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-106b-3p ggCAGTGCGtgtgcc CCGCACUG m7b (m7b->m6b) HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-521 ggcAGTGCGTgtgcc AACGCACU m7b Disrupted HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-603 ggcAGTGTGTGtgcc CACACACU m8a Created HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-8485 ggcagTGTGTGTGcc CACACACA m8a Created HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-106b-3p ggCAGTGCGtgtgcc CCGCACUG m7b (m7b->m6b) HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-521 ggcAGTGCGTgtgcc AACGCACU m7b Disrupted HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-603 ggcAGTGTGTGtgcc CACACACU m8a Created HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-8485 ggcagTGTGTGTGcc CACACACA m8a Created HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086074T>G COSM1104459 TCGA-AX-A05Z-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4764-3p tgaaGGAGTTAtggg UUAACUCC m7b Created HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-500a-5p tgAAGGATTtatggg UAAUCCUU m7b (m7b->m6b) HHHNA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-4764-3p tgaaGGAGTTAtggg UUAACUCC m7b Created HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-500a-5p tgAAGGATTtatggg UAAUCCUU m7b (m7b->m6b) HHHNE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-4764-3p tgaaGGAGTTAtggg UUAACUCC m7b Created HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-500a-5p tgAAGGATTtatggg UAAUCCUU m7b (m7b->m6b) HHHSA_22265_TNC|NM_002160|exon_CDS|-7.95663895621028|0.226383980260863
hsa-miR-4764-3p tgaaGGAGTTAtggg UUAACUCC m7b Created HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265
hsa-miR-500a-5p tgAAGGATTtatggg UAAUCCUU m7b (m7b->m6b) HHHSE_19272_TNC|NM_002160|exon_CDS|-7.05735601868207|-1.5990059927265

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086034A>G COSM201990 TCGA-A6-2676-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4252 ccCAGTGGCtgtcat GGCCACUG m7b (m6b->m7b) HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4645-3p cccagtgACTGTCat AGACAGUA m6b Disrupted HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4691-3p cccaGTGGCTGtcat CCAGCCAC m7b Created HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4704-3p cccaGTGACTGtcat UCAGUCAC m7b Disrupted HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4252 ccCAGTGGCtgtcat GGCCACUG m7b (m6b->m7b) HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4645-3p cccagtgACTGTCat AGACAGUA m6b Disrupted HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4691-3p cccaGTGGCTGtcat CCAGCCAC m7b Created HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4704-3p cccaGTGACTGtcat UCAGUCAC m7b Disrupted HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086025G>A COSM3321484 SNU-175 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3187-3p tgtcATGGCCAgggc UUGGCCAU m7b Disrupted HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-3190-5p tgtcaTGGCCAGggc UCUGGCCA m7b Disrupted HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4529-5p tgtcATGGCCagggc AGGCCAUC m6b Disrupted HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-3187-3p tgtcATGGCCAgggc UUGGCCAU m7b Disrupted HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-3190-5p tgtcaTGGCCAGggc UCUGGCCA m7b Disrupted HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4529-5p tgtcATGGCCagggc AGGCCAUC m6b Disrupted HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115086008G>T COSM1624471 BN06T [liver][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3678-5p ctgcgTGTACGGcca UCCGUACA m7b Created HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-3678-5p ctgcgTGTACGGcca UCCGUACA m7b Created HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115085988C>G COSM4152006 AOCS-147-1-1 [ovary][NS][other][neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-221-5p tcTGCCAGGagggct ACCUGGCA m7b (m6b->m7b) HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4290 tctgccaGGAGGGCt UGCCCUCC m7b Created HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4655-3p tctgccACGAGGGct ACCCUCGU m7b Disrupted HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4667-3p tctgccAGGAGGGct UCCCUCCU m7b Created HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4720-5p tcTGCCAGGagggct CCUGGCAU m7a (m6a->m7a) HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-660-3p tctgcCAGGAGGgct ACCUCCUG m7b Created HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-6868-5p tCTGCCAGgagggct ACUGGCAG m7b Created HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-8073 tcTGCCAGGagggct ACCUGGCA m7b (m6b->m7b) HHHNA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-221-5p tcTGCCAGGagggct ACCUGGCA m7b (m6b->m7b) HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4290 tctgccaGGAGGGCt UGCCCUCC m7b Created HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4655-3p tctgccACGAGGGct ACCCUCGU m7b Disrupted HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4667-3p tctgccAGGAGGGct UCCCUCCU m7b Created HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-4720-5p tcTGCCAGGagggct CCUGGCAU m7a (m6a->m7a) HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-660-3p tctgcCAGGAGGgct ACCUCCUG m7b Created HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-6868-5p tCTGCCAGgagggct ACUGGCAG m7b Created HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077
hsa-miR-8073 tcTGCCAGGagggct ACCUGGCA m7b (m6b->m7b) HHHSA_22264_TNC|NM_002160|exon_CDS|-7.31139391804321|-0.314301785378077

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115084414C>T COSM3926039 TCGA-QB-A6FS-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1915-3p acctggCCTGGGaca CCCCAGGG m6b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-1972 accTGGCCTGggaca UCAGGCCA m7b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4726-3p acctggCCTGGGaca ACCCAGGU m6b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-6840-3p acctggCCTGGGaca GCCCAGGA m6b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-1915-3p acctggCCTGGGaca CCCCAGGG m6b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-1972 accTGGCCTGggaca UCAGGCCA m7b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4726-3p acctggCCTGGGaca ACCCAGGU m6b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-6840-3p acctggCCTGGGaca GCCCAGGA m6b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115084408C>A COSM140629 cSCCP8 [skin][ear][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1250-3p cctggGAAAATGaga ACAUUUUC m7b Created HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4289 cctgggACAATGaga GCAUUGUG m6b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4433a-5p ccTGGGACaatgaga CGUCCCAC m6b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4433b-5p ccTGGGACAatgaga AUGUCCCA m7b (m7b->m6b) HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4446-5p cctGGGAAAatgaga AUUUCCCU m6b Created HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4646-3p cctGGGACAATgaga AUUGUCCC m8a Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-5696 cctgggaAAATGAGa CUCAUUUA m7a Created HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-7977 cCTGGGAAaatgaga UUCCCAGC m7a Created HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-1250-3p cctggGAAAATGaga ACAUUUUC m7b Created HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4289 cctgggACAATGaga GCAUUGUG m6b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4433a-5p ccTGGGACaatgaga CGUCCCAC m6b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4433b-5p ccTGGGACAatgaga AUGUCCCA m7b (m7b->m6b) HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4446-5p cctGGGAAAatgaga AUUUCCCU m6b Created HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4646-3p cctGGGACAATgaga AUUGUCCC m8a Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-5696 cctgggaAAATGAGa CUCAUUUA m7a Created HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-7977 cCTGGGAAaatgaga UUCCCAGC m7a Created HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115084404G>A COSM3653432 TCGA-EE-A29B-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4289 ggACAATGagatgcg GCAUUGUG m6b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-5701 gGACAATAAgatgcg UUAUUGUC m8a (m7a->m8a) HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-6758-3p ggacAATGAGatgcg ACUCAUUC m6b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4289 ggACAATGagatgcg GCAUUGUG m6b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-5701 gGACAATAAgatgcg UUAUUGUC m8a (m7a->m8a) HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-6758-3p ggacAATGAGatgcg ACUCAUUC m6b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115084390A>T COSM1104458 TCGA-BK-A0C9-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3664-5p gggtcACAGAGTacc AACUCUGU m7b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4264 gggtcACTGAGTacc ACUCAGUC m7a Created HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4276 gggTCACTGAGtacc CUCAGUGA m8a Created HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4714-5p gggtcaCAGAGTacc AACUCUGA m6b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-512-5p gggtcaCTGAGTacc CACUCAGC m6b Created HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-5190 ggGTCACTGagtacc CCAGUGAC m7b (m6b->m7b) HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-6808-3p gGGTCACAgagtacc GUGUGACC m7b Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-7973 GGGTCACAgagtacc UGUGACCC m8a Disrupted HHHNE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-3664-5p gggtcACAGAGTacc AACUCUGU m7b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4264 gggtcACTGAGTacc ACUCAGUC m7a Created HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4276 gggTCACTGAGtacc CUCAGUGA m8a Created HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-4714-5p gggtcaCAGAGTacc AACUCUGA m6b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-512-5p gggtcaCTGAGTacc CACUCAGC m6b Created HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-5190 ggGTCACTGagtacc CCAGUGAC m7b (m6b->m7b) HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-6808-3p gGGTCACAgagtacc GUGUGACC m7b Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742
hsa-miR-7973 GGGTCACAgagtacc UGUGACCC m8a Disrupted HHHSE_19271_TNC|NM_002160|exon_CDS|-7.81204931475824|-1.09068348183742

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115081804G>C COSM4644883 LIM2551 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1538 aataccCCGGGCCct CGGCCCGG m7b Created HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-296-5p aatacccGGGGCCCt AGGGCCCC m7b Disrupted HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-4745-3p aataccCCGGGCCct UGGCCCGG m7b Created HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-503-3p AATACCCCgggccct GGGGUAUU m8a Created HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-5587-3p aataCCCGGGGCcct GCCCCGGG m8a Disrupted HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-1538 aataccCCGGGCCct CGGCCCGG m7b Created HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-296-5p aatacccGGGGCCCt AGGGCCCC m7b Disrupted HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-4745-3p aataccCCGGGCCct UGGCCCGG m7b Created HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-503-3p AATACCCCgggccct GGGGUAUU m8a Created HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-5587-3p aataCCCGGGGCcct GCCCCGGG m8a Disrupted HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-1538 aataccCCGGGCCct CGGCCCGG m7b Created HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-296-5p aatacccGGGGCCCt AGGGCCCC m7b Disrupted HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-4745-3p aataccCCGGGCCct UGGCCCGG m7b Created HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-503-3p AATACCCCgggccct GGGGUAUU m8a Created HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-5587-3p aataCCCGGGGCcct GCCCCGGG m8a Disrupted HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-1538 aataccCCGGGCCct CGGCCCGG m7b Created HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-296-5p aatacccGGGGCCCt AGGGCCCC m7b Disrupted HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-4745-3p aataccCCGGGCCct UGGCCCGG m7b Created HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-503-3p AATACCCCgggccct GGGGUAUU m8a Created HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-5587-3p aataCCCGGGGCcct GCCCCGGG m8a Disrupted HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821

Mutation Mutation ID Sample Name Cancer Type
chr9:g.115081802G>A COSM1701574 YUKLAB [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-296-5p tacccGGGGCCCTgg AGGGCCCC m8a Disrupted HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-3918 tacccggGGCCCTGg ACAGGGCC m7b Disrupted HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-5088-5p tacccgGAGCCCTGg CAGGGCUC m8a Created HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-5587-3p taCCCGGGGCcctgg GCCCCGGG m8a Disrupted HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-7160-3p tacccgGGGCCCTGg CAGGGCCC m8a Disrupted HHHNA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-296-5p tacccGGGGCCCTgg AGGGCCCC m8a Disrupted HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-3918 tacccggGGCCCTGg ACAGGGCC m7b Disrupted HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-5088-5p tacccgGAGCCCTGg CAGGGCUC m8a Created HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-5587-3p taCCCGGGGCcctgg GCCCCGGG m8a Disrupted HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-7160-3p tacccgGGGCCCTGg CAGGGCCC m8a Disrupted HHHNE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-296-5p tacccGGGGCCCTgg AGGGCCCC m8a Disrupted HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-3918 tacccggGGCCCTGg ACAGGGCC m7b Disrupted HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-5088-5p tacccgGAGCCCTGg CAGGGCUC m8a Created HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-5587-3p taCCCGGGGCcctgg GCCCCGGG m8a Disrupted HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-7160-3p tacccgGGGCCCTGg CAGGGCCC m8a Disrupted HHHSA_22263_TNC|NM_002160|exon_CDS|-8.02104251323174|1.37613134010852
hsa-miR-296-5p tacccGGGGCCCTgg AGGGCCCC m8a Disrupted HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-3918 tacccggGGCCCTGg ACAGGGCC m7b Disrupted HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-5088-5p tacccgGAGCCCTGg CAGGGCUC m8a Created HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-5587-3p taCCCGGGGCcctgg GCCCCGGG m8a Disrupted HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821
hsa-miR-7160-3p tacccgGGGCCCTGg CAGGGCCC m8a Disrupted HHHSE_19270_TNC|NM_002160|exon_CDS|-7.81652392377934|0.584147043715821

*By default, only target sites identified by TargetScan are displayed. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.

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