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_0069766
Gene Symbol: KIT
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Browse Pathways

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr4:g.54737210C>A COSM4755662 pfg073T [stomach][NS][carcinoma][diffuse_adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2909 gcagatcCCCTAAaa GUUAGGGC m6b Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4278 gcagatCCCCTAaaa CUAGGGGG m6b Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6509-5p gcagatcACCTAAaa AUUAGGUA m6b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6783-5p gcagaTCCCCTAaaa UAGGGGAA m7a Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6789-5p gcagatCCCCTAaaa GUAGGGGC m6b Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6800-5p gcagaTCACCTAaaa GUAGGUGA m7b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6802-5p gcagatCACCTAaaa CUAGGUGG m6b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6824-5p gcagaTCCCCTAaaa GUAGGGGA m7b Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-2909 gcagatcCCCTAAaa GUUAGGGC m6b Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4278 gcagatCCCCTAaaa CUAGGGGG m6b Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6509-5p gcagatcACCTAAaa AUUAGGUA m6b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6783-5p gcagaTCCCCTAaaa UAGGGGAA m7a Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6789-5p gcagatCCCCTAaaa GUAGGGGC m6b Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6800-5p gcagaTCACCTAaaa GUAGGUGA m7b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6802-5p gcagatCACCTAaaa CUAGGUGG m6b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6824-5p gcagaTCCCCTAaaa GUAGGGGA m7b Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-2909 gcagatcCCCTAAaa GUUAGGGC m6b Disrupted HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-4278 gcagatCCCCTAaaa CUAGGGGG m6b Disrupted HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6509-5p gcagatcACCTAAaa AUUAGGUA m6b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6783-5p gcagaTCCCCTAaaa UAGGGGAA m7a Disrupted HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6789-5p gcagatCCCCTAaaa GUAGGGGC m6b Disrupted HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6800-5p gcagaTCACCTAaaa GUAGGUGA m7b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6802-5p gcagatCACCTAaaa CUAGGUGG m6b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6824-5p gcagaTCCCCTAaaa GUAGGGGA m7b Disrupted HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54737208T>C COSM1430194 TCGA-CM-5862-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4278 atgcagaCCCCCTAa CUAGGGGG m7b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4527 atGCAGACCccctaa UGGUCUGC m7b (m6b->m7b) HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4716-3p atgcagaCCCCCTaa AAGGGGGA m6b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6503-5p atGCAGACCccctaa AGGUCUGC m7b (m6b->m7b) HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6732-5p atgcagACCCCCTAa UAGGGGGU m8a Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6783-5p atgcagaTCCCCTAa UAGGGGAA m7a Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6794-5p atgcagaCCCCCTaa CAGGGGGA m6b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6805-5p atgcagaCCCCCTAa UAGGGGGC m7a Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6824-5p atgcagaTCCCCTAa GUAGGGGA m7b Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6835-5p atgcagACCCCCTaa AGGGGGUA m7a Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4278 atgcagaCCCCCTAa CUAGGGGG m7b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4527 atGCAGACCccctaa UGGUCUGC m7b (m6b->m7b) HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4716-3p atgcagaCCCCCTaa AAGGGGGA m6b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6503-5p atGCAGACCccctaa AGGUCUGC m7b (m6b->m7b) HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6732-5p atgcagACCCCCTAa UAGGGGGU m8a Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6783-5p atgcagaTCCCCTAa UAGGGGAA m7a Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6794-5p atgcagaCCCCCTaa CAGGGGGA m6b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6805-5p atgcagaCCCCCTAa UAGGGGGC m7a Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6824-5p atgcagaTCCCCTAa GUAGGGGA m7b Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-6835-5p atgcagACCCCCTaa AGGGGGUA m7a Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4278 atgcagaCCCCCTAa CUAGGGGG m7b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-4527 atGCAGACCccctaa UGGUCUGC m7b (m6b->m7b) HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-4716-3p atgcagaCCCCCTaa AAGGGGGA m6b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6503-5p atGCAGACCccctaa AGGUCUGC m7b (m6b->m7b) HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6732-5p atgcagACCCCCTAa UAGGGGGU m8a Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6783-5p atgcagaTCCCCTAa UAGGGGAA m7a Disrupted HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6794-5p atgcagaCCCCCTaa CAGGGGGA m6b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6805-5p atgcagaCCCCCTAa UAGGGGGC m7a Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6824-5p atgcagaTCCCCTAa GUAGGGGA m7b Disrupted HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-6835-5p atgcagACCCCCTaa AGGGGGUA m7a Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54737207A>G COSM1430193 TCGA-AZ-5403-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3144-5p gatgcaGGTCCCCTa AGGGGACC m8a Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-3649 gatgcAGGTCCCcta AGGGACCU m7b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4652-5p gatgcagGTCCCCTa AGGGGACU m7a Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-492 gatgCAGGTCCccta AGGACCUG m7b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-3144-5p gatgcaGGTCCCCTa AGGGGACC m8a Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-3649 gatgcAGGTCCCcta AGGGACCU m7b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4652-5p gatgcagGTCCCCTa AGGGGACU m7a Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-492 gatgCAGGTCCccta AGGACCUG m7b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-3144-5p gatgcaGGTCCCCTa AGGGGACC m8a Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-3649 gatgcAGGTCCCcta AGGGACCU m7b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-4652-5p gatgcagGTCCCCTa AGGGGACU m7a Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-492 gatgCAGGTCCccta AGGACCUG m7b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54737206G>T COSM29358 1196414 [haematopoietic_and_lymphoid_tissue][NS][haematopoietic_neoplasm][myeloproliferative_neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-20a-3p ggATGCAGatcccct ACUGCAUU m6b Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-3201 ggatgCATATCCCct GGGAUAUG m8a Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4791 ggatgCATATCCcct UGGAUAUG m7b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-20a-3p ggATGCAGatcccct ACUGCAUU m6b Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-3201 ggatgCATATCCCct GGGAUAUG m8a Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4791 ggatgCATATCCcct UGGAUAUG m7b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-20a-3p ggATGCAGatcccct ACUGCAUU m6b Disrupted HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-3201 ggatgCATATCCCct GGGAUAUG m8a Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184
hsa-miR-4791 ggatgCATATCCcct UGGAUAUG m7b Created HHKTA_42201_NM_000222|2814|2853|1.8172535241738|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54737188A>G COSM1430192 TCGA-DM-A1DA-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1264 cataatgAAGACTTg CAAGUCUU m7b Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-136-5p catAATGGAGacttg ACUCCAUU m7b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-3184-3p cataatgGAGACTTg AAAGUCUC m7b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4528 cATAATGAagacttg UCAUUAUA m7a Disrupted HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-1264 cataatgAAGACTTg CAAGUCUU m7b Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-136-5p catAATGGAGacttg ACUCCAUU m7b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-3184-3p cataatgGAGACTTg AAAGUCUC m7b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4528 cATAATGAagacttg UCAUUAUA m7a Disrupted HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54737187G>A COSM4844805 TCGA-IR-A3LA-01 [cervix][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4528 acATAATGAagactt UCAUUAUA m7a (m7a->m6a) HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4795-3p acATAATAaagactt AUAUUAUU m6b Created HHHNE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4528 acATAATGAagactt UCAUUAUA m7a (m7a->m6a) HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975
hsa-miR-4795-3p acATAATAaagactt AUAUUAUU m6b Created HHHSE_9508_KIT|NM_000222|exon_CDS|-5.06846077370125|-0.773698681829975

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54736573T>C COSM29359 1196420 [haematopoietic_and_lymphoid_tissue][NS][haematopoietic_neoplasm][myeloproliferative_neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1296-5p cgtctGGCCCTAtgg UUAGGGCC m7b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-4512 cgtctGGCCCTatgg CAGGGCCU m6b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-4640-5p cgtCTGGCCCtatgg UGGGCCAG m7b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-4726-5p cgtCTGGCCCTatgg AGGGCCAG m8a Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-6895-5p cgtcTGGCCCTatgg CAGGGCCA m7b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-7160-3p cgtctGGCCCTatgg CAGGGCCC m6b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-1296-5p cgtctGGCCCTAtgg UUAGGGCC m7b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-4512 cgtctGGCCCTatgg CAGGGCCU m6b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-4640-5p cgtCTGGCCCtatgg UGGGCCAG m7b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-4726-5p cgtCTGGCCCTatgg AGGGCCAG m8a Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-6895-5p cgtcTGGCCCTatgg CAGGGCCA m7b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-7160-3p cgtctGGCCCTatgg CAGGGCCC m6b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54736571G>A COSM133767 1609818 [skin][mucosal][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3117-3p gacgtctAGTCCTAt AUAGGACU m7b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-4759 gacgtcTAGTCCTAt UAGGACUA m8a Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-6503-3p gacgtCTAGTCCtat GGGACUAG m7b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-8083 gacgtctAGTCCTat CAGGACUU m6b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-3117-3p gacgtctAGTCCTAt AUAGGACU m7b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-4759 gacgtcTAGTCCTAt UAGGACUA m8a Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-6503-3p gacgtCTAGTCCtat GGGACUAG m7b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-8083 gacgtctAGTCCTat CAGGACUU m6b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
Mutation Mutation ID Sample Name Cancer Type
chr4:g.54736567G>A COSM1734911 ACINAR01 [pancreas][NS][carcinoma][acinar_carcinoma]
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
chr4:g.54736558G>T COSM133781 1610020 [skin][chronically_sun_exposed_site][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-424-3p cACGTTTTaaagtga CAAAACGU m7b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-548ad-3p caCGTTTTaaagtga GAAAACGA m6b Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-607 cacgTTTGAAagtga GUUCAAAU m6b Disrupted HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-6715b-3p cacGTTTGAaagtga CUCAAACC m6b Disrupted HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-424-3p cACGTTTTaaagtga CAAAACGU m7b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-548ad-3p caCGTTTTaaagtga GAAAACGA m6b Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-607 cacgTTTGAAagtga GUUCAAAU m6b Disrupted HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-6715b-3p cacGTTTGAaagtga CUCAAACC m6b Disrupted HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54736555T>C COSM133756 1609715 [skin][acral][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-498 atacacGCTTGAAAg UUUCAAGC m8a Created HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-607 atacacgTTTGAAag GUUCAAAU m6b Disrupted HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-6715b-3p atacacGTTTGAaag CUCAAACC m6b Disrupted HHHNE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-498 atacacGCTTGAAAg UUUCAAGC m8a Created HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-607 atacacgTTTGAAag GUUCAAAU m6b Disrupted HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898
hsa-miR-6715b-3p atacacGTTTGAaag CUCAAACC m6b Disrupted HHHSE_9507_KIT|NM_000222|exon_CDS|-4.35408453416683|-1.97452426216898

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54731897C>T COSM4937975 TCGA-DD-A11D-01 [liver][NS][carcinoma][hepatocellular_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1908-5p tgtgactCCCGCCat CGGCGGGG m6b Disrupted HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-224-5p tGTGACTTccgccat CAAGUCAC m7b Created HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-25-5p tgtgactTCCGCCat AGGCGGAG m6b Created HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-4730 tgtgactTCCGCCAt CUGGCGGA m7b Created HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-663a tgtgactCCCGCCat AGGCGGGG m6b Disrupted HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-1908-5p tgtgactCCCGCCat CGGCGGGG m6b Disrupted HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-224-5p tGTGACTTccgccat CAAGUCAC m7b Created HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-25-5p tgtgactTCCGCCat AGGCGGAG m6b Created HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-4730 tgtgactTCCGCCAt CUGGCGGA m7b Created HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-663a tgtgactCCCGCCat AGGCGGGG m6b Disrupted HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54731880T>C COSM19111 988233 [haematopoietic_and_lymphoid_tissue][NS][haematopoietic_neoplasm][acute_myeloid_leukaemia]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-223-5p tcATACACagaaaga CGUGUAUU m6b Created HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-3924 tcATACATAgaaaga AUAUGUAU m7b (m7b->m6b) HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-4652-3p tcatacACAGAAaga GUUCUGUU m6b Created HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-7159-3p tcataCATAGAAAga UUUCUAUG m8a Disrupted HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-223-5p tcATACACagaaaga CGUGUAUU m6b Created HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-3924 tcATACATAgaaaga AUAUGUAU m7b (m7b->m6b) HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-4652-3p tcatacACAGAAaga GUUCUGUU m6b Created HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-7159-3p tcataCATAGAAAga UUUCUAUG m8a Disrupted HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54731879A>G COSM1430175 TCGA-CK-5915-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-297 ctCATACATagaaag AUGUAUGU m7a (m7a->m6a) HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-3924 ctcATACATAgaaag AUAUGUAU m7b Disrupted HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-7159-3p ctcataCATAGAAAg UUUCUAUG m8a Disrupted HHHNE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-297 ctCATACATagaaag AUGUAUGU m7a (m7a->m6a) HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-3924 ctcATACATAgaaag AUAUGUAU m7b Disrupted HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525
hsa-miR-7159-3p ctcataCATAGAAAg UUUCUAUG m8a Disrupted HHHSE_9506_KIT|NM_000222|exon_CDS|-5.45806125264653|1.01544499994525

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729455A>C COSM1235167 15D [haematopoietic_and_lymphoid_tissue][spleen][lymphoid_neoplasm][marginal_zone_lymphoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-340-5p CTTTATAAgaatctt UUAUAAAG m8a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729453T>C COSM3767902 RK176_C01 [liver][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-340-5p caCTTTATAAgaatc UUAUAAAG m8a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-5590-3p cACTTTATaagaatc AAUAAAGU m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-578 cactttACAAGAAtc CUUCUUGU m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-643 cacttTACAAGaatc ACUUGUAU m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-142-5p cACTTTATaagaatc CAUAAAGU m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-340-5p caCTTTATAAgaatc UUAUAAAG m8a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-5590-3p cACTTTATaagaatc AAUAAAGU m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-578 cactttACAAGAAtc CUUCUUGU m7b Created HPKTA_45387_G48906.1_55595608
hsa-miR-643 cacttTACAAGaatc ACUUGUAU m6b Created HPKTA_45387_G48906.1_55595608

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729446C>A COSM1581111 DLBCL799 [haematopoietic_and_lymphoid_tissue][NS][lymphoid_neoplasm][diffuse_large_B_cell_lymphoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-5000-5p gaagCTGAACTttat CAGUUCAG m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-5047 gaAGCTGCActttat UUGCAGCU m7b (m7b->m6b) HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-519a-3p gaagcTGCACTTTat AAAGUGCA m8a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-519b-3p gaagcTGCACTTTat AAAGUGCA m8a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-519c-3p gaagcTGCACTTTat AAAGUGCA m8a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-519d-3p gaagctGCACTTTat CAAAGUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-520a-3p gaagctGCACTTTat AAAGUGCU m7a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-520b gaagctGCACTTTat AAAGUGCU m7a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-520c-3p gaagctGCACTTTat AAAGUGCU m7a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-520d-3p gaagctGCACTTTat AAAGUGCU m7a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-520e gaagctGCACTTTat AAAGUGCU m7a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-526b-3p gaagctGCACTTTat GAAAGUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-548ah-5p gaagctgCACTTTat AAAAGUGA m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-548at-5p gaagctgAACTTTat AAAAGUUA m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-561-3p gaagctgAACTTTat CAAAGUUU m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-93-5p gaagctGCACTTTat CAAAGUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-106a-5p gaagctGCACTTTat AAAAGUGC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-106b-5p gaagctGCACTTTAt UAAAGUGC m8a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-1301-3p gaAGCTGCActttat UUGCAGCU m7b (m7b->m6b) HPKTA_45387_G48906.1_55595608
hsa-miR-148a-5p gaagctGAACTTTat AAAGUUCU m7a Created HPKTA_45387_G48906.1_55595608
hsa-miR-17-5p gaagctGCACTTTat CAAAGUGC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-20a-5p gaagctGCACTTTAt UAAAGUGC m8a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-20b-5p gaagctGCACTTTat CAAAGUGC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-3609 gaagctgCACTTTat CAAAGUGA m6b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-372-3p gaagctGCACTTTat AAAGUGCU m7a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-3944-5p gaaGCTGCACtttat UGUGCAGC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-5000-5p gaagCTGAACTttat CAGUUCAG m7b Created HPKTA_45387_G48906.1_55595608
hsa-miR-5047 gaAGCTGCActttat UUGCAGCU m7b (m7b->m6b) HPKTA_45387_G48906.1_55595608
hsa-miR-519a-3p gaagcTGCACTTTat AAAGUGCA m8a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-519b-3p gaagcTGCACTTTat AAAGUGCA m8a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-519c-3p gaagcTGCACTTTat AAAGUGCA m8a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-519d-3p gaagctGCACTTTat CAAAGUGC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-520a-3p gaagctGCACTTTat AAAGUGCU m7a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-520b gaagctGCACTTTat AAAGUGCU m7a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-520c-3p gaagctGCACTTTat AAAGUGCU m7a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-520d-3p gaagctGCACTTTat AAAGUGCU m7a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-520e gaagctGCACTTTat AAAGUGCU m7a Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-526b-3p gaagctGCACTTTat GAAAGUGC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-548ah-5p gaagctgCACTTTat AAAAGUGA m6b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-548at-5p gaagctgAACTTTat AAAAGUUA m6b Created HPKTA_45387_G48906.1_55595608
hsa-miR-561-3p gaagctgAACTTTat CAAAGUUU m6b Created HPKTA_45387_G48906.1_55595608
hsa-miR-93-5p gaagctGCACTTTat CAAAGUGC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-106a-5p gaagctGCACTTTat AAAAGUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-106b-5p gaagctGCACTTTAt UAAAGUGC m8a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-1301-3p gaAGCTGCActttat UUGCAGCU m7b (m7b->m6b) HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-148a-5p gaagctGAACTTTat AAAGUUCU m7a Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-17-5p gaagctGCACTTTat CAAAGUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-20a-5p gaagctGCACTTTAt UAAAGUGC m8a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-20b-5p gaagctGCACTTTat CAAAGUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3609 gaagctgCACTTTat CAAAGUGA m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-372-3p gaagctGCACTTTat AAAGUGCU m7a Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3944-5p gaaGCTGCACtttat UGUGCAGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729442G>T COSM1291927 CLL014 [haematopoietic_and_lymphoid_tissue][NS][lymphoid_neoplasm][chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-10b-3p tgcaGAATCTGcact ACAGAUUC m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-1301-3p tgcagaAGCTGCAct UUGCAGCU m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3944-5p tgcagaaGCTGCACt UGUGCAGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-5047 tgcagaAGCTGCAct UUGCAGCU m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-544a TGCAGAATctgcact AUUCUGCA m8a Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-10b-3p tgcaGAATCTGcact ACAGAUUC m7b Created HPKTA_45387_G48906.1_55595608
hsa-miR-1301-3p tgcagaAGCTGCAct UUGCAGCU m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-3944-5p tgcagaaGCTGCACt UGUGCAGC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-5047 tgcagaAGCTGCAct UUGCAGCU m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-544a TGCAGAATctgcact AUUCUGCA m8a Created HPKTA_45387_G48906.1_55595608

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729438A>G COSM327109 TLE43 [haematopoietic_and_lymphoid_tissue][NS][lymphoid_neoplasm][acute_lymphoblastic_T_cell_leukaemia]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-20a-3p atcATGCAGaagctg ACUGCAUU m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-544a atcaTGCAGAAgctg AUUCUGCA m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-20a-3p atcATGCAGaagctg ACUGCAUU m6b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-544a atcaTGCAGAAgctg AUUCUGCA m7b Disrupted HPKTA_45387_G48906.1_55595608

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729435T>C COSM1430169 TCGA-DM-A285-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-20a-3p aagatcATGCAGaag ACUGCAUU m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-4520-5p aagatCACGCAGaag CCUGCGUG m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-544a aagatcaTGCAGAAg AUUCUGCA m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6076 aagaTCATGCagaag AGCAUGAC m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-20a-3p aagatcATGCAGaag ACUGCAUU m6b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-4520-5p aagatCACGCAGaag CCUGCGUG m7b Created HPKTA_45387_G48906.1_55595608
hsa-miR-544a aagatcaTGCAGAAg AUUCUGCA m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-6076 aagaTCATGCagaag AGCAUGAC m6b Disrupted HPKTA_45387_G48906.1_55595608

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729434A>G COSM1430168 TCGA-DM-A28E-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-20a-3p gaagatcATGCAGaa ACUGCAUU m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3130-3p gaagatcGTGCAGaa GCUGCACC m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-4793-3p gaagatcGTGCAGAa UCUGCACU m7a Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6076 gaagaTCATGCagaa AGCAUGAC m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-20a-3p gaagatcATGCAGaa ACUGCAUU m6b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-3130-3p gaagatcGTGCAGaa GCUGCACC m6b Created HPKTA_45387_G48906.1_55595608
hsa-miR-4793-3p gaagatcGTGCAGAa UCUGCACU m7a Created HPKTA_45387_G48906.1_55595608
hsa-miR-6076 gaagaTCATGCagaa AGCAUGAC m6b Disrupted HPKTA_45387_G48906.1_55595608

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729433C>T COSM36053 TCGA-DY-A0XA-01 [large_intestine][rectum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6076 ggaagaTCATGCaga AGCAUGAC m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6076 ggaagaTCATGCaga AGCAUGAC m6b Disrupted HPKTA_45387_G48906.1_55595608

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729433C>G COSM1430167 TCGA-A6-6654-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-141-5p GGAAGATGatgcaga CAUCUUCC m8a Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6076 ggaagaTCATGCaga AGCAUGAC m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-141-5p GGAAGATGatgcaga CAUCUUCC m8a Created HPKTA_45387_G48906.1_55595608
hsa-miR-6076 ggaagaTCATGCaga AGCAUGAC m6b Disrupted HPKTA_45387_G48906.1_55595608

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729432TC>T COSM29443 1194930 [soft_tissue][fibrous_tissue_and_uncertain_origin][gastrointestinal_stromal_tumour][spindle]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-153-3p aggaagaTATGCAga UUGCAUAG m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-448 aggaagATATGCAga UUGCAUAU m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6076 aggaagaTCATGCaga AGCAUGAC m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-141-5p aGGAAGATcatgcaga CAUCUUCC m7b Disrupted HPKTA_45387_G48906.1_55595608
hsa-miR-153-3p aggaagaTATGCAga UUGCAUAG m6b Created HPKTA_45387_G48906.1_55595608
hsa-miR-448 aggaagATATGCAga UUGCAUAU m7b Created HPKTA_45387_G48906.1_55595608
hsa-miR-6076 aggaagaTCATGCaga AGCAUGAC m6b Disrupted HPKTA_45387_G48906.1_55595608

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729429A>G COSM1430166 TCGA-AD-6901-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-141-5p agcaGGAAGATcatg CAUCUUCC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-1976 aGCAGGAGGatcatg CCUCCUGC m8a (m7a->m8a) HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3074-5p aGCAGGAAgatcatg GUUCCUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3653-5p agCAGGAGGatcatg CCUCCUGA m7a (m6a->m7a) HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-660-3p agCAGGAGGatcatg ACCUCCUG m7b (m6b->m7b) HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729428A>G COSM1430165 TCGA-CK-5915-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-141-5p aagcaGGAAGATcat CAUCUUCC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3074-5p aaGCAGGAAgatcat GUUCCUGC m7b (m7b->m6b) HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-4469 aagcAGGGAGatcat GCUCCCUC m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6867-3p aagcAGGGAGAtcat CUCUCCCU m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6893-3p aAGCAGGGagatcat CCCUGCUG m7a Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-7113-3p aagCAGGGAGatcat CCUCCCUG m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-7641 aagcaggGAGATCAt UUGAUCUC m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729427G>T COSM1056104 TCGA-BS-A0UF-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-141-5p aaagcaGGAAGATca CAUCUUCC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-200a-5p aaagcaGTAAGATca CAUCUUAC m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-200b-5p aaagcaGTAAGATca CAUCUUAC m7b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3074-5p aaaGCAGGAAgatca GUUCCUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-370-3p aaAGCAGGaagatca GCCUGCUG m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6893-3p aaAGCAGGaagatca CCCUGCUG m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729427G>A COSM96878 1516525 [soft_tissue][fibrous_tissue_and_uncertain_origin][gastrointestinal_stromal_tumour][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-141-5p aaagcaGGAAGATca CAUCUUCC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-3074-5p aaaGCAGGAAgatca GUUCCUGC m7b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-370-3p aaAGCAGGaagatca GCCUGCUG m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-544a aaaGCAGAAagatca AUUCUGCA m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6071 aaAGCAGAAagatca UUCUGCUG m7a (m6a->m7a) HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6738-3p aaaGCAGAAagatca CUUCUGCC m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6828-3p aaAGCAGAaagatca AUCUGCUC m6b Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-6893-3p aaAGCAGGaagatca CCCUGCUG m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729420A>G COSM1430164 TCGA-CK-5915-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1251-3p tttgttCAAAGCagg CGCUUUGC m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54729419C>T COSM96879 1516527 [soft_tissue][fibrous_tissue_and_uncertain_origin][gastrointestinal_stromal_tumour][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1251-3p atttgttCAAAGCag CGCUUUGC m6b Disrupted HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184
hsa-miR-495-3p aTTTGTTTaaagcag AAACAAAC m7a Created HHKTA_16792_NM_000222|2160|2199|4.28352616412395|0.120988641640184

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54727856T>A COSM734166 TCGA-85-6561-01 [lung][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-7159-5p gggaaggTTGTTGAg UUCAACAA m7b Disrupted HHHNE_9505_KIT|NM_000222|exon_CDS|-4.85198223275564|1.04953766028055
hsa-miR-7159-5p gggaaggTTGTTGAg UUCAACAA m7b Disrupted HHHSE_9505_KIT|NM_000222|exon_CDS|-4.85198223275564|1.04953766028055

Mutation Mutation ID Sample Name Cancer Type
chr4:g.54727848C>T COSM1179694 SWE-34 [prostate][NS][adenoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-186-3p gagctTTTGGGaagg GCCCAAAG m6b Created HHHNE_9505_KIT|NM_000222|exon_CDS|-4.85198223275564|1.04953766028055
hsa-miR-186-3p gagctTTTGGGaagg GCCCAAAG m6b Created HHHSE_9505_KIT|NM_000222|exon_CDS|-4.85198223275564|1.04953766028055

*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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