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: hsa_circ_0063404
Gene Symbol: TNRC6B
Browse Associations

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr22:g.40262171CA>C COSM1632609 RK065_C01 [liver][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-221-5p actgcGCCAGGTaagg ACCUGGCA m7a Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-619-3p actgcgCCAGGTaagg GACCUGGA m6b Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-6722-5p acTGCGCCaggtaagg AGGCGCAC m6b Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-7851-3p actgcgCCAGGTAagg UACCUGGG m7a Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-8073 actgcGCCAGGTaagg ACCUGGCA m7a Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-221-5p actgcGCCAGGTaagg ACCUGGCA m7a Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-619-3p actgcgCCAGGTaagg GACCUGGA m6b Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-6722-5p acTGCGCCaggtaagg AGGCGCAC m6b Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-7851-3p actgcgCCAGGTAagg UACCUGGG m7a Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-8073 actgcGCCAGGTaagg ACCUGGCA m7a Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-221-5p actgcGCCAGGTaagg ACCUGGCA m7a Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-619-3p actgcgCCAGGTaagg GACCUGGA m6b Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-6722-5p acTGCGCCaggtaagg AGGCGCAC m6b Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-7851-3p actgcgCCAGGTAagg UACCUGGG m7a Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-8073 actgcGCCAGGTaagg ACCUGGCA m7a Disrupted HHHNE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-221-5p actgcGCCAGGTaagg ACCUGGCA m7a Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-619-3p actgcgCCAGGTaagg GACCUGGA m6b Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-6722-5p acTGCGCCaggtaagg AGGCGCAC m6b Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-7851-3p actgcgCCAGGTAagg UACCUGGG m7a Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522
hsa-miR-8073 actgcGCCAGGTaagg ACCUGGCA m7a Disrupted HHHSE_19448_TNRC6B|NM_001162501|exon_CDS|-7.38955042331275|-1.29645064255522

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40262124C>T COSM4965361 PCSI_0328_Pa_P_526 [pancreas][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-147b caaacaaCGCACAag GUGUGCGG m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-210-3p caaacaACGCACAag CUGUGCGU m7b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-33a-5p caaaCAATGCACaag GUGCAUUG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-33b-5p caaaCAATGCACaag GUGCAUUG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-4289 caaACAATGCacaag GCAUUGUG m7a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-147b caaacaaCGCACAag GUGUGCGG m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-210-3p caaacaACGCACAag CUGUGCGU m7b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-33a-5p caaaCAATGCACaag GUGCAUUG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-33b-5p caaaCAATGCACaag GUGCAUUG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-4289 caaACAATGCacaag GCAUUGUG m7a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-147b caaacaaCGCACAag GUGUGCGG m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-210-3p caaacaACGCACAag CUGUGCGU m7b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-33a-5p caaaCAATGCACaag GUGCAUUG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-33b-5p caaaCAATGCACaag GUGCAUUG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-4289 caaACAATGCacaag GCAUUGUG m7a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40262097C>A COSM4882609 OSCC-GB_01060111 [upper_aerodigestive_tract][mouth][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-143-5p ctccCTGCACagcac GGUGCAGU m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-4270 CTCCCTGAacagcac UCAGGGAG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-6132 ctCCCTGCacagcac AGCAGGGC m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-143-5p ctccCTGCACagcac GGUGCAGU m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-4270 CTCCCTGAacagcac UCAGGGAG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-6132 ctCCCTGCacagcac AGCAGGGC m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-143-5p ctccCTGCACagcac GGUGCAGU m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-4270 CTCCCTGAacagcac UCAGGGAG m8a Created HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234
hsa-miR-6132 ctCCCTGCacagcac AGCAGGGC m6b Disrupted HHKTA_41698_NM_001162501|587|626|1.8172535241738|0.161288724932234

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40262014G>T COSM4998973 PDA_019 [pancreas][NS][carcinoma][ductal_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3692-5p CCAGCAGGaccacaa CCUGCUGG m8a Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-370-3p cCAGCAGGaccacaa GCCUGCUG m7b Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-4536-5p ccagcagTACCACAa UGUGGUAG m7a Created HPSLC_12509_G14808.1_40658019
hsa-miR-6893-3p cCAGCAGGaccacaa CCCUGCUG m7b Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-93-3p cCAGCAGTaccacaa ACUGCUGA m7a Created HPSLC_12509_G14808.1_40658019
hsa-miR-3692-5p CCAGCAGGaccacaa CCUGCUGG m8a Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-370-3p cCAGCAGGaccacaa GCCUGCUG m7b Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-4536-5p ccagcagTACCACAa UGUGGUAG m7a Created HPSLC_12509_G14808.1_40658019
hsa-miR-6893-3p cCAGCAGGaccacaa CCCUGCUG m7b Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-93-3p cCAGCAGTaccacaa ACUGCUGA m7a Created HPSLC_12509_G14808.1_40658019
hsa-miR-3692-5p CCAGCAGGaccacaa CCUGCUGG m8a Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-370-3p cCAGCAGGaccacaa GCCUGCUG m7b Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-4536-5p ccagcagTACCACAa UGUGGUAG m7a Created HPSLC_12509_G14808.1_40658019
hsa-miR-6893-3p cCAGCAGGaccacaa CCCUGCUG m7b Disrupted HPSLC_12509_G14808.1_40658019
hsa-miR-93-3p cCAGCAGTaccacaa ACUGCUGA m7a Created HPSLC_12509_G14808.1_40658019

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40246021G>A COSM1034343 TCGA-AP-A059-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1248 gagAGAAGGagcaag ACCUUCUU m6b Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-130b-5p gagaGAAAGAGcaag ACUCUUUC m7b Created HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-4268 gagagaAGGAGCaag GGCUCCUC m6b Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-4448 gagagAAGGAGCaag GGCUCCUU m7b Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-6772-3p gagagaAGGAGCAAg UUGCUCCU m8a Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-6868-3p gagAGAAGGAgcaag UUCCUUCU m7b Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-1248 gagAGAAGGagcaag ACCUUCUU m6b Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-130b-5p gagaGAAAGAGcaag ACUCUUUC m7b Created HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-4268 gagagaAGGAGCaag GGCUCCUC m6b Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-4448 gagagAAGGAGCaag GGCUCCUU m7b Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-6772-3p gagagaAGGAGCAAg UUGCUCCU m8a Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-6868-3p gagAGAAGGAgcaag UUCCUUCU m7b Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-1248 gagAGAAGGagcaag ACCUUCUU m6b Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-130b-5p gagaGAAAGAGcaag ACUCUUUC m7b Created HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-4268 gagagaAGGAGCaag GGCUCCUC m6b Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-4448 gagagAAGGAGCaag GGCUCCUU m7b Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-6772-3p gagagaAGGAGCAAg UUGCUCCU m8a Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-6868-3p gagAGAAGGAgcaag UUCCUUCU m7b Disrupted HHHNA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-1248 gagAGAAGGagcaag ACCUUCUU m6b Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-130b-5p gagaGAAAGAGcaag ACUCUUUC m7b Created HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-4268 gagagaAGGAGCaag GGCUCCUC m6b Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-4448 gagagAAGGAGCaag GGCUCCUU m7b Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-6772-3p gagagaAGGAGCAAg UUGCUCCU m8a Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487
hsa-miR-6868-3p gagAGAAGGAgcaag UUCCUUCU m7b Disrupted HHHSA_15786_TNRC6B|NM_001162501|exon_CDS|-5.97675517430101|1.20265697415487

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40203171C>T COSN4785340 tumor_4121361 [haematopoietic_and_lymphoid_tissue][NS][lymphoid_neoplasm][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-203b-3p ctggtAGTTCAAaac UUGAACUG m7a Created HHRBL_9565_BCBL1-2of3-SCL_4344
hsa-miR-610 ctggTAGCTCAaaac UGAGCUAA m7a Disrupted HHRBL_9565_BCBL1-2of3-SCL_4344
hsa-miR-7158-3p ctggTAGTTCAaaac CUGAACUA m7b Created HHRBL_9565_BCBL1-2of3-SCL_4344
hsa-miR-8055 ctggtaGCTCAAAac CUUUGAGC m7b Disrupted HHRBL_9565_BCBL1-2of3-SCL_4344

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40178060A>AT COSN1262147 HCC39T [liver][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3646 agaaTTCATTTTttg AAAAUGAA m8a Disrupted HHFKP_94771_cluster-15333_3_37
hsa-miR-3662 agaatTCATTTTttg GAAAAUGA m7b Disrupted HHFKP_94771_cluster-15333_3_37
hsa-miR-3646 agaaTTCATTTTttg AAAAUGAA m8a Disrupted HHKTA_2862_NM_001162501|133|172|21.4176308206198|0.161288724932234
hsa-miR-3662 agaatTCATTTTttg GAAAAUGA m7b Disrupted HHKTA_2862_NM_001162501|133|172|21.4176308206198|0.161288724932234

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40156173A>C COSM3152536 SNU-C2B [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1273e ggtgaagCAAGCAAa UUGCUUGA m7a Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3160-5p ggtgaAGAAAGCaaa GGCUUUCU m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3977 ggTGAAGCAagcaaa GUGCUUCA m7b (m6b->m7b) HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4327 ggtgaaGCAAGCaaa GGCUUGCA m6b Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6754-3p GGTGAAGAaagcaaa UCUUCACC m8a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6875-3p ggtGAAGAAagcaaa AUUCUUCC m6b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1273e ggtgaagCAAGCAAa UUGCUUGA m7a Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3160-5p ggtgaAGAAAGCaaa GGCUUUCU m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3977 ggTGAAGCAagcaaa GUGCUUCA m7b (m6b->m7b) HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4327 ggtgaaGCAAGCaaa GGCUUGCA m6b Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6754-3p GGTGAAGAaagcaaa UCUUCACC m8a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6875-3p ggtGAAGAAagcaaa AUUCUUCC m6b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1273e ggtgaagCAAGCAAa UUGCUUGA m7a Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3160-5p ggtgaAGAAAGCaaa GGCUUUCU m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3977 ggTGAAGCAagcaaa GUGCUUCA m7b (m6b->m7b) HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4327 ggtgaaGCAAGCaaa GGCUUGCA m6b Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6754-3p GGTGAAGAaagcaaa UCUUCACC m8a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6875-3p ggtGAAGAAagcaaa AUUCUUCC m6b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1273e ggtgaagCAAGCAAa UUGCUUGA m7a Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3160-5p ggtgaAGAAAGCaaa GGCUUUCU m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3977 ggTGAAGCAagcaaa GUGCUUCA m7b (m6b->m7b) HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4327 ggtgaaGCAAGCaaa GGCUUGCA m6b Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6754-3p GGTGAAGAaagcaaa UCUUCACC m8a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6875-3p ggtGAAGAAagcaaa AUUCUUCC m6b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40156169G>A COSM1416386 TCGA-AD-6901-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1226-3p tcCTGGTGAagaaag UCACCAGC m7a (m7a->m6a) HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-412-3p tcctGGTGAAGaaag ACUUCACC m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4733-3p tCCTGGTGaagaaag CCACCAGG m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6753-5p tCCTGGTGaagaaag CACCAGGG m7a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6754-3p tcctGGTGAAGAaag UCUUCACC m8a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6837-3p tcctgGTGAAGaaag CCUUCACU m6b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6875-3p tcctggtGAAGAAag AUUCUUCC m6b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1226-3p tcCTGGTGAagaaag UCACCAGC m7a (m7a->m6a) HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1911-3p tCCTGGTGaagaaag CACCAGGC m7a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-412-3p tcctGGTGAAGaaag ACUUCACC m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4733-3p tCCTGGTGaagaaag CCACCAGG m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6753-5p tCCTGGTGaagaaag CACCAGGG m7a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6754-3p tcctGGTGAAGAaag UCUUCACC m8a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6837-3p tcctgGTGAAGaaag CCUUCACU m6b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6875-3p tcctggtGAAGAAag AUUCUUCC m6b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1226-3p tcCTGGTGAagaaag UCACCAGC m7a (m7a->m6a) HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1911-3p tCCTGGTGaagaaag CACCAGGC m7a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-412-3p tcctGGTGAAGaaag ACUUCACC m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4733-3p tCCTGGTGaagaaag CCACCAGG m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6753-5p tCCTGGTGaagaaag CACCAGGG m7a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6754-3p tcctGGTGAAGAaag UCUUCACC m8a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6837-3p tcctgGTGAAGaaag CCUUCACU m6b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6875-3p tcctggtGAAGAAag AUUCUUCC m6b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1226-3p tcCTGGTGAagaaag UCACCAGC m7a (m7a->m6a) HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-1911-3p tCCTGGTGaagaaag CACCAGGC m7a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-412-3p tcctGGTGAAGaaag ACUUCACC m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4733-3p tCCTGGTGaagaaag CCACCAGG m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6753-5p tCCTGGTGaagaaag CACCAGGG m7a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6754-3p tcctGGTGAAGAaag UCUUCACC m8a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6837-3p tcctgGTGAAGaaag CCUUCACU m6b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-6875-3p tcctggtGAAGAAag AUUCUUCC m6b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537

Mutation Mutation ID Sample Name Cancer Type
chr22:g.40156153G>A COSM3152531 KM12 [large_intestine][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-19a-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19b-1-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19b-2-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3198 atggcaaGACTCCAc GUGGAGUC m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4294 atggcaAGACTCCac GGGAGUCU m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4309 atggcaaGACTCCAc CUGGAGUC m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-431-5p atgGCAAGACtccac UGUCUUGC m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4776-3p ATGGCAAGactccac CUUGCCAU m8a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-924 atggcAAGACTCcac AGAGUCUU m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19a-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19b-1-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19b-2-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3198 atggcaaGACTCCAc GUGGAGUC m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4294 atggcaAGACTCCac GGGAGUCU m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4309 atggcaaGACTCCAc CUGGAGUC m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-431-5p atgGCAAGACtccac UGUCUUGC m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4776-3p ATGGCAAGactccac CUUGCCAU m8a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-924 atggcAAGACTCcac AGAGUCUU m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19a-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19b-1-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19b-2-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3198 atggcaaGACTCCAc GUGGAGUC m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4294 atggcaAGACTCCac GGGAGUCU m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4309 atggcaaGACTCCAc CUGGAGUC m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-431-5p atgGCAAGACtccac UGUCUUGC m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4776-3p ATGGCAAGactccac CUUGCCAU m8a Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-924 atggcAAGACTCcac AGAGUCUU m7b Disrupted HHHNA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19a-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19b-1-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-19b-2-5p atgGCAAAACTccac AGUUUUGC m8a Created HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-3198 atggcaaGACTCCAc GUGGAGUC m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4294 atggcaAGACTCCac GGGAGUCU m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4309 atggcaaGACTCCAc CUGGAGUC m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-431-5p atgGCAAGACtccac UGUCUUGC m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-4776-3p ATGGCAAGactccac CUUGCCAU m8a Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537
hsa-miR-924 atggcAAGACTCcac AGAGUCUU m7b Disrupted HHHSA_15784_TNRC6B|NM_001024843|exon_CDS|-7.25335235595057|1.30203680586537

*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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