SomamiR DB 2.0
Somatic mutations altering microRNA-ceRNA interactions
  Home Search Help Download  

PolymiRTS Database
Prediction criteria: TargetScan sites only     All 6mer or longer seed matches
Transcript ID: hsa_circ_0028136
Gene Symbol: UBE3B
Browse Associations
Browse Pathways

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr12:g.109499748G>C COSM691318 TCGA-21-1076-01 [lung][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3182 ctCAGAAGaagtcca GCUUCUGU m6b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4273 ctcAGAACAagtcca GUGUUCUC m6b Created HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4659a-3p ctcAGAAGAAgtcca UUUCUUCU m7b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4659b-3p ctcAGAAGAAgtcca UUUCUUCU m7b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4762-3p cTCAGAAGaagtcca CUUCUGAU m7a Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4778-3p ctcaGAAGAAGtcca UCUUCUUC m7b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-6505-3p ctcagaAGAAGTCca UGACUUCU m7b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-6739-3p ctcAGAACAAgtcca AUUGUUCU m7b Created HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-3182 ctCAGAAGaagtcca GCUUCUGU m6b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4273 ctcAGAACAagtcca GUGUUCUC m6b Created HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4659a-3p ctcAGAAGAAgtcca UUUCUUCU m7b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4659b-3p ctcAGAAGAAgtcca UUUCUUCU m7b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4762-3p cTCAGAAGaagtcca CUUCUGAU m7a Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4778-3p ctcaGAAGAAGtcca UCUUCUUC m7b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-6505-3p ctcagaAGAAGTCca UGACUUCU m7b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-6739-3p ctcAGAACAAgtcca AUUGUUCU m7b Created HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565

Mutation Mutation ID Sample Name Cancer Type
chr12:g.109499743C>T COSM3810951 TCGA-AC-A23H-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3182 tgtgtctCAGAAGaa GCUUCUGU m6b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-3617-5p tgTGTCTTagaagaa AAAGACAU m6b Created HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4251 tgtgTCTCAGaagaa CCUGAGAA m6b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4263 tgtgtCTTAGAAgaa AUUCUAAG m7b Created HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4329 tgtGTCTCAGaagaa CCUGAGAC m7b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4762-3p tgtgtcTCAGAAGaa CUUCUGAU m7a Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-641 tgTGTCTTagaagaa AAAGACAU m6b Created HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-6761-5p tgtgTCTCAGAagaa UCUGAGAG m7a Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-3182 tgtgtctCAGAAGaa GCUUCUGU m6b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-3617-5p tgTGTCTTagaagaa AAAGACAU m6b Created HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4251 tgtgTCTCAGaagaa CCUGAGAA m6b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4263 tgtgtCTTAGAAgaa AUUCUAAG m7b Created HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4329 tgtGTCTCAGaagaa CCUGAGAC m7b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4762-3p tgtgtcTCAGAAGaa CUUCUGAU m7a Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-641 tgTGTCTTagaagaa AAAGACAU m6b Created HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-6761-5p tgtgTCTCAGAagaa UCUGAGAG m7a Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-3182 tgtgtctCAGAAGaa GCUUCUGU m6b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-3617-5p tgTGTCTTagaagaa AAAGACAU m6b Created HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4251 tgtgTCTCAGaagaa CCUGAGAA m6b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4263 tgtgtCTTAGAAgaa AUUCUAAG m7b Created HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4329 tgtGTCTCAGaagaa CCUGAGAC m7b Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4762-3p tgtgtcTCAGAAGaa CUUCUGAU m7a Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-641 tgTGTCTTagaagaa AAAGACAU m6b Created HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-6761-5p tgtgTCTCAGAagaa UCUGAGAG m7a Disrupted HHHNE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-3182 tgtgtctCAGAAGaa GCUUCUGU m6b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-3617-5p tgTGTCTTagaagaa AAAGACAU m6b Created HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4251 tgtgTCTCAGaagaa CCUGAGAA m6b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4263 tgtgtCTTAGAAgaa AUUCUAAG m7b Created HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4329 tgtGTCTCAGaagaa CCUGAGAC m7b Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-4762-3p tgtgtcTCAGAAGaa CUUCUGAU m7a Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-641 tgTGTCTTagaagaa AAAGACAU m6b Created HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565
hsa-miR-6761-5p tgtgTCTCAGAagaa UCUGAGAG m7a Disrupted HHHSE_20211_UBE3B|NM_130466|exon_CDS|-5.56168013670765|-1.56172679168565

Mutation Mutation ID Sample Name Cancer Type
chr12:g.109491088C>T COSM3455865 TCGA-GN-A26C-01 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1261 tgtcTATCCAaaggc AUGGAUAA m6b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-5004-3p tgtctATCCAAaggc CUUGGAUU m6b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-5191 tgtCTATCCaaaggc AGGAUAGG m6b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-5585-3p tgtCTATTCAaaggc CUGAAUAG m7b Created HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-1261 tgtcTATCCAaaggc AUGGAUAA m6b Disrupted HPRO6_19371_G22575.1_109928895
hsa-miR-5004-3p tgtctATCCAAaggc CUUGGAUU m6b Disrupted HPRO6_19371_G22575.1_109928895
hsa-miR-5191 tgtCTATCCaaaggc AGGAUAGG m6b Disrupted HPRO6_19371_G22575.1_109928895
hsa-miR-5585-3p tgtCTATTCAaaggc CUGAAUAG m7b Created HPRO6_19371_G22575.1_109928895
hsa-miR-1261 tgtcTATCCAaaggc AUGGAUAA m6b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-5004-3p tgtctATCCAAaggc CUUGGAUU m6b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-5191 tgtCTATCCaaaggc AGGAUAGG m6b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-5585-3p tgtCTATTCAaaggc CUGAAUAG m7b Created HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-1261 tgtcTATCCAaaggc AUGGAUAA m6b Disrupted HPRO6_19371_G22575.1_109928895
hsa-miR-5004-3p tgtctATCCAAaggc CUUGGAUU m6b Disrupted HPRO6_19371_G22575.1_109928895
hsa-miR-5191 tgtCTATCCaaaggc AGGAUAGG m6b Disrupted HPRO6_19371_G22575.1_109928895
hsa-miR-5585-3p tgtCTATTCAaaggc CUGAAUAG m7b Created HPRO6_19371_G22575.1_109928895
Mutation Mutation ID Sample Name Cancer Type
chr12:g.109491082G>A COSM368564 LUAD-NYU1051S [lung][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
chr12:g.109491075C>T COSM4641614 LIM2405 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-8080 aagacccTGTCCTTg GAAGGACA m7b Created HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-1182 aAGACCCTgtccttg GAGGGUCU m7b Created HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-8080 aagacccTGTCCTTg GAAGGACA m7b Created HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544

Mutation Mutation ID Sample Name Cancer Type
chr12:g.109491066G>A COSM1492747 TCGA-A3-3346-01 [kidney][NS][carcinoma][clear_cell_renal_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1202 tggcCTGGCAagacc GUGCCAGC m6b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-1972 TGGCCTGAcaagacc UCAGGCCA m8a Created HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-3655 tggcctGACAAGacc GCUUGUCG m6b Created HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-3972 tggcCTGGCAagacc CUGCCAGC m6b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-431-5p tggcctgGCAAGACc UGUCUUGC m7b Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-4755-3p tgGCCTGGCaagacc AGCCAGGC m7b (m7b->m6b) HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-4776-3p tggccTGGCAAGacc CUUGCCAU m7a Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544
hsa-miR-5006-5p tggCCTGGCAAgacc UUGCCAGG m8a Disrupted HHKTA_41224_NM_130466|1254|1293|1.86052146522556|0.420657831355544

*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.

Genome Browser