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_005563
Gene Symbol: STMN1
Browse Pathways

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr1:g.25903712C>T COSM3487431 TCGA-D3-A2JF-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1249-5p cctttcCCCTCCaaa AGGAGGGA m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-1270 cctttccTCTCCAaa CUGGAGAU m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-185-5p cctttcCTCTCCAaa UGGAGAGA m7a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-1914-3p cctttCCCCTCCaaa GGAGGGGU m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3125 cctTTCCTCTccaaa UAGAGGAA m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3153 cCTTTCCCCtccaaa GGGGAAAG m8a (m8a->m7a) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3916 cctTTCCTCTccaaa AAGAGGAA m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4306 cctttcCTCTCCAaa UGGAGAGA m7a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4443 cctttccCCTCCAAa UUGGAGGC m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4531 cctttccTCTCCAaa AUGGAGAA m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4644 cctttcCTCTCCAaa UGGAGAGA m7a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-5192 cctttcCTCTCCaaa AGGAGAGU m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-620 cctttccTCTCCAaa AUGGAGAU m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6515-5p cctttcCCCTCCAAa UUGGAGGG m8a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6733-5p cCTTTCCCctccaaa UGGGAAAG m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6739-5p cCTTTCCCctccaaa UGGGAAAG m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6783-5p cctTTCCCCTccaaa UAGGGGAA m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6797-5p cctttcCCCTCCaaa AGGAGGGA m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6859-5p cctTTCCTCTCcaaa GAGAGGAA m8a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-1249-5p cctttcCCCTCCaaa AGGAGGGA m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-1270 cctttccTCTCCAaa CUGGAGAU m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-185-5p cctttcCTCTCCAaa UGGAGAGA m7a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-1914-3p cctttCCCCTCCaaa GGAGGGGU m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3125 cctTTCCTCTccaaa UAGAGGAA m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3153 cCTTTCCCCtccaaa GGGGAAAG m8a (m8a->m7a) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3916 cctTTCCTCTccaaa AAGAGGAA m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4306 cctttcCTCTCCAaa UGGAGAGA m7a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4443 cctttccCCTCCAAa UUGGAGGC m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4531 cctttccTCTCCAaa AUGGAGAA m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4644 cctttcCTCTCCAaa UGGAGAGA m7a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-5192 cctttcCTCTCCaaa AGGAGAGU m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-620 cctttccTCTCCAaa AUGGAGAU m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6515-5p cctttcCCCTCCAAa UUGGAGGG m8a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6733-5p cCTTTCCCctccaaa UGGGAAAG m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6739-5p cCTTTCCCctccaaa UGGGAAAG m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6783-5p cctTTCCCCTccaaa UAGGGGAA m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6797-5p cctttcCCCTCCaaa AGGAGGGA m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6859-5p cctTTCCTCTCcaaa GAGAGGAA m8a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25903697G>A COSM366951 LUAD-F00282 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1248 gAAGAAGGatctttc ACCUUCUU m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4659a-3p gaAGAAGAAtctttc UUUCUUCU m7b (m6b->m7b) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4659b-3p gaAGAAGAAtctttc UUUCUUCU m7b (m6b->m7b) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4778-3p GAAGAAGAatctttc UCUUCUUC m8a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6868-3p gaAGAAGGAtctttc UUCCUUCU m7b (m7b->m6b) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25903687T>G COSM3487429 TCGA-EE-A3JA-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1247-3p cttTCCCGGGaggaa CCCCGGGA m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4532 ctttCCCGGGaggaa CCCCGGGG m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4685-5p ctttCCCTGGaggaa CCCAGGGC m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4691-5p ctttcccTGGAGGAa GUCCUCCA m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-5584-5p cTTTCCCTGgaggaa CAGGGAAA m8a (m8a->m7a) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6749-3p ctttcccGGGAGGAa CUCCUCCC m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6754-5p cttTCCCTGGaggaa CCAGGGAG m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6792-3p ctttcccTGGAGGAa CUCCUCCA m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6837-5p ctttCCCTGGaggaa ACCAGGGC m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-7113-5p cttTCCCTGGAggaa UCCAGGGA m8a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-1247-3p cttTCCCGGGaggaa CCCCGGGA m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4532 ctttCCCGGGaggaa CCCCGGGG m6b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4685-5p ctttCCCTGGaggaa CCCAGGGC m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4691-5p ctttcccTGGAGGAa GUCCUCCA m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-5584-5p cTTTCCCTGgaggaa CAGGGAAA m8a (m8a->m7a) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6749-3p ctttcccGGGAGGAa CUCCUCCC m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6754-5p cttTCCCTGGaggaa CCAGGGAG m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6792-3p ctttcccTGGAGGAa CUCCUCCA m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6837-5p ctttCCCTGGaggaa ACCAGGGC m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-7113-5p cttTCCCTGGAggaa UCCAGGGA m8a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25903655G>T COSM4655212 SW403 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1205 agCTGCAGAagaaag UCUGCAGG m7a (m7a->m6a) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3158-5p agCTGCAGaagaaag CCUGCAGA m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3182 agctgCAGAAGaaag GCUUCUGU m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4659a-3p agctgcAGAAGAAAg UUUCUUCU m8a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4659b-3p agctgcAGAAGAAAg UUUCUUCU m8a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-491-3p agcTGCATAAGaaag CUUAUGCA m8a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-544a agcTGCAGAAgaaag AUUCUGCA m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6738-3p agctGCAGAAGaaag CUUCUGCC m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6875-3p agctgcaGAAGAAag AUUCUUCC m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-1205 agCTGCAGAagaaag UCUGCAGG m7a (m7a->m6a) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3158-5p agCTGCAGaagaaag CCUGCAGA m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3182 agctgCAGAAGaaag GCUUCUGU m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4659a-3p agctgcAGAAGAAAg UUUCUUCU m8a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4659b-3p agctgcAGAAGAAAg UUUCUUCU m8a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-491-3p agcTGCATAAGaaag CUUAUGCA m8a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-544a agcTGCAGAAgaaag AUUCUGCA m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6738-3p agctGCAGAAGaaag CUUCUGCC m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6875-3p agctgcaGAAGAAag AUUCUUCC m6b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25903645G>A COSM4030915 TCGA-BR-4256-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1915-5p gaaagacGCAAGGTa ACCUUGCC m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3200-3p gaaagacGCAAGGTa CACCUUGC m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4711-3p gaAAGACACaaggta CGUGUCUU m7b (m6b->m7b) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-511-5p gAAAGACACaaggta GUGUCUUU m8a (m7a->m8a) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-581 gaaagACACAAGgta UCUUGUGU m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-599 gaaaGACACAAggta GUUGUGUC m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6830-3p GAAAGACAcaaggta UGUCUUUC m8a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6841-3p gaaagacGCAAGGTa ACCUUGCA m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-1915-5p gaaagacGCAAGGTa ACCUUGCC m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-3200-3p gaaagacGCAAGGTa CACCUUGC m7b Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-4711-3p gaAAGACACaaggta CGUGUCUU m7b (m6b->m7b) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-511-5p gAAAGACACaaggta GUGUCUUU m8a (m7a->m8a) HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-581 gaaagACACAAGgta UCUUGUGU m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-599 gaaaGACACAAggta GUUGUGUC m7b Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6830-3p GAAAGACAcaaggta UGUCUUUC m8a Created HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528
hsa-miR-6841-3p gaaagacGCAAGGTa ACCUUGCA m7a Disrupted HHHSH_3724_STMN1|NM_001145454|exon_CDS|-8.93776669054819|0.265542671435528

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25901054G>T COSM175313 HT115 [large_intestine][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4320 gaacaaAGAATCCaa GGGAUUCU m7b Disrupted HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227
hsa-miR-6844 gaACAAAGAAtccaa UUCUUUGU m8a Disrupted HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25901050C>G COSM4816459 TCGA-IR-A3LK-01 [cervix][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-33a-5p aaagAATGCAaagac GUGCAUUG m6b Created HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227
hsa-miR-33b-5p aaagAATGCAaagac GUGCAUUG m6b Created HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227
hsa-miR-3680-3p aaagaATGCAAAgac UUUUGCAU m7b Created HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227
hsa-miR-4320 aaAGAATCCaaagac GGGAUUCU m7b (m7b->m6b) HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227
hsa-miR-5004-3p aaagAATCCAAagac CUUGGAUU m7b Disrupted HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25901033G>T COSM4930296 TCGA-MI-A75I-01 [liver][NS][carcinoma][hepatocellular_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-554 tgctGACTAGactga GCUAGUCC m6b Created HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25901029C>A COSM907547 TCGA-AP-A059-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-622 gacgAGACTGaagct ACAGUCUG m6b Disrupted HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25901016A>C COSM907546 TCGA-BS-A0UF-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3973 ctgacTACTTTGTtc ACAAAGUA m8a Created HHHSH_3722_STMN1|NM_005563|exon_utr3|-8.06355030688519|0.539025245641681
hsa-miR-7-1-3p ctgactaATTTGTTc CAACAAAU m7b Disrupted HHHSH_3722_STMN1|NM_005563|exon_utr3|-8.06355030688519|0.539025245641681
hsa-miR-7-2-3p ctgactaATTTGTTc CAACAAAU m7b Disrupted HHHSH_3722_STMN1|NM_005563|exon_utr3|-8.06355030688519|0.539025245641681
hsa-miR-3973 ctgacTACTTTGTtc ACAAAGUA m8a Created HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227
hsa-miR-7-1-3p ctgactaATTTGTTc CAACAAAU m7b Disrupted HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227
hsa-miR-7-2-3p ctgactaATTTGTTc CAACAAAU m7b Disrupted HHHSH_3723_STMN1|NM_005563|exon_CDS|-8.92441829710251|0.741905663638227

Mutation Mutation ID Sample Name Cancer Type
chr1:g.25900737T>C COSN7989665 PCSI_0083_Pa_P_526 [pancreas][NS][carcinoma][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.
*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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