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_0011531
Gene Symbol: SFPQ
Browse Associations

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr1:g.35189320G>A COSM1667389 HCC2998 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-7160-5p tCTCAGCAatggaag UGCUGAGG m7a Created HHHNA_678_SFPQ|NM_005066|exon_CDS|-7.77001842908859|0.776039154861503
hsa-miR-628-5p tcTCAGCAatggaag AUGCUGAC m6b Created HHHNA_678_SFPQ|NM_005066|exon_CDS|-7.77001842908859|0.776039154861503
hsa-miR-181a-3p tctcagCGATGGaag ACCAUCGA m6b Disrupted HHHNA_678_SFPQ|NM_005066|exon_CDS|-7.77001842908859|0.776039154861503
hsa-miR-7160-5p tCTCAGCAatggaag UGCUGAGG m7a Created HHHSA_678_SFPQ|NM_005066|exon_CDS|-7.77001842908859|0.776039154861503
hsa-miR-628-5p tcTCAGCAatggaag AUGCUGAC m6b Created HHHSA_678_SFPQ|NM_005066|exon_CDS|-7.77001842908859|0.776039154861503
hsa-miR-181a-3p tctcagCGATGGaag ACCAUCGA m6b Disrupted HHHSA_678_SFPQ|NM_005066|exon_CDS|-7.77001842908859|0.776039154861503

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35189270A>C COSM1342124 TCGA-AA-3510-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-19b-1-5p agttgaaCAAAACat AGUUUUGC m6b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-19b-2-5p agttgaaCAAAACat AGUUUUGC m6b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-335-3p agtTGAAAAAaacat UUUUUCAU m7a Disrupted HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-375 agttGAACAAAacat UUUGUUCG m7a Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-6739-3p agttGAACAAaacat AUUGUUCU m6b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-19a-5p agttgaaCAAAACat AGUUUUGC m6b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-1305 aGTTGAAAAaaacat UUUUCAAC m8a (m8a->m7a) HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-1305 aGTTGAAAAaaacat UUUUCAAC m8a (m8a->m7a) HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-19a-5p agttgaaCAAAACat AGUUUUGC m6b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-19b-1-5p agttgaaCAAAACat AGUUUUGC m6b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-19b-2-5p agttgaaCAAAACat AGUUUUGC m6b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-335-3p agtTGAAAAAaacat UUUUUCAU m7a Disrupted HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-375 agttGAACAAAacat UUUGUUCG m7a Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-6739-3p agttGAACAAaacat AUUGUUCU m6b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35189258G>A COSM168446 TCGA-AG-A002-01 [large_intestine][rectum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-33b-5p catgaaaAATGCAaa GUGCAUUG m6b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-33a-5p catgaaaAATGCAaa GUGCAUUG m6b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-335-3p cATGAAAAAtgcaaa UUUUUCAU m8a (m7a->m8a) HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-153-5p catgAAAAATGcaaa UCAUUUUU m7b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-335-3p cATGAAAAAtgcaaa UUUUUCAU m8a (m7a->m8a) HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-33a-5p catgaaaAATGCAaa GUGCAUUG m6b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-33b-5p catgaaaAATGCAaa GUGCAUUG m6b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-153-5p catgAAAAATGcaaa UCAUUUUU m7b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35189247C>T COSM908659 TCGA-AP-A0LT-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-511-5p caAAAGACAaattgg GUGUCUUU m7b (m7b->m6b) HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-6830-3p caAAAGACAaattgg UGUCUUUC m7a (m7a->m6a) HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-511-5p caAAAGACAaattgg GUGUCUUU m7b (m7b->m6b) HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-6830-3p caAAAGACAaattgg UGUCUUUC m7a (m7a->m6a) HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35189236G>A COSM1195101 H1155 [lung][NS][carcinoma][large_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1250-3p ttgGAAAATGaaatg ACAUUUUC m7b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-153-5p ttggAAAATGAaatg UCAUUUUU m7a Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-5696 ttggaAAATGAaatg CUCAUUUA m6b Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-579-3p ttggaAAATGAAatg UUCAUUUG m7a Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-664b-3p ttggaAAATGAAatg UUCAUUUG m7a Created HHHNA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-1250-3p ttgGAAAATGaaatg ACAUUUUC m7b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-153-5p ttggAAAATGAaatg UCAUUUUU m7a Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-5696 ttggaAAATGAaatg CUCAUUUA m6b Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-579-3p ttggaAAATGAAatg UUCAUUUG m7a Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596
hsa-miR-664b-3p ttggaAAATGAAatg UUCAUUUG m7a Created HHHSA_677_SFPQ|NM_005066|exon_CDS|-7.72243760443278|-0.871929107322596

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35189046C>A COSM4599999 UM-SCC-47 [upper_aerodigestive_tract][mouth][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1257 ggaagaaATTCACaa AGUGAAUG m6b Created HHHNE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-148a-5p ggaAGAACTTcacaa AAAGUUCU m7b Disrupted HHHNE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-183-3p ggaagaAATTCACaa GUGAAUUA m7a Created HHHNE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-22-5p gGAAGAACTtcacaa AGUUCUUC m8a (m8a->m7a) HHHNE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-3611 ggaagaaCTTCACAa UUGUGAAG m7b Disrupted HHHNE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-5584-3p ggAAGAACTtcacaa UAGUUCUU m7b (m7b->m6b) HHHNE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-1257 ggaagaaATTCACaa AGUGAAUG m6b Created HHHSE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-148a-5p ggaAGAACTTcacaa AAAGUUCU m7b Disrupted HHHSE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-183-3p ggaagaAATTCACaa GUGAAUUA m7a Created HHHSE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-22-5p gGAAGAACTtcacaa AGUUCUUC m8a (m8a->m7a) HHHSE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-3611 ggaagaaCTTCACAa UUGUGAAG m7b Disrupted HHHSE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-5584-3p ggAAGAACTtcacaa UAGUUCUU m7b (m7b->m6b) HHHSE_16524_SFPQ|NM_005066|exon_CDS|-7.95014589970043|0.336415871163509
hsa-miR-1257 ggaagaaATTCACaa AGUGAAUG m6b Created HHKTA_51035_NM_005066|1718|1757|1.34130617260447|7.21304004917053
hsa-miR-148a-5p ggaAGAACTTcacaa AAAGUUCU m7b Disrupted HHKTA_51035_NM_005066|1718|1757|1.34130617260447|7.21304004917053
hsa-miR-183-3p ggaagaAATTCACaa GUGAAUUA m7a Created HHKTA_51035_NM_005066|1718|1757|1.34130617260447|7.21304004917053
hsa-miR-22-5p gGAAGAACTtcacaa AGUUCUUC m8a (m8a->m7a) HHKTA_51035_NM_005066|1718|1757|1.34130617260447|7.21304004917053
hsa-miR-3611 ggaagaaCTTCACAa UUGUGAAG m7b Disrupted HHKTA_51035_NM_005066|1718|1757|1.34130617260447|7.21304004917053
hsa-miR-5584-3p ggAAGAACTtcacaa UAGUUCUU m7b (m7b->m6b) HHKTA_51035_NM_005066|1718|1757|1.34130617260447|7.21304004917053

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35188077C>T COSM1225442 587278 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-598-3p ggaggaATGACGTAg UACGUCAU m8a Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-598-3p ggaggaATGACGTAg UACGUCAU m8a Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-598-3p ggaggaATGACGTAg UACGUCAU m8a Created HHKTA_10544_NM_005066|1791|1830|6.31711939355653|7.21304004917053

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35188067AAG>G COSM426152 TCGA-A1-A0SO-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1236-3p gacgtaGAAGAGaggaa CCUCUUCC m6b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-155-3p gacGTAGGAGaggaa CUCCUACA m7a Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-4279 gacgtAGGAGAGgaa CUCUCCUC m7a Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6845-3p gacgtAGGAGAGGaa CCUCUCCU m8a Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-7111-3p gacgtagGAGAGGAa AUCCUCUC m7b Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-1236-3p gacgtaGAAGAGaggaa CCUCUUCC m6b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-155-3p gacGTAGGAGaggaa CUCCUACA m7a Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4279 gacgtAGGAGAGgaa CUCUCCUC m7a Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6845-3p gacgtAGGAGAGGaa CCUCUCCU m8a Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-7111-3p gacgtagGAGAGGAa AUCCUCUC m7b Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-1236-3p gacgtaGAAGAGaggaa CCUCUUCC m6b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-155-3p gacGTAGGAGaggaa CUCCUACA m7a Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-4279 gacgtAGGAGAGgaa CUCUCCUC m7a Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6845-3p gacgtAGGAGAGGaa CCUCUCCU m8a Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-7111-3p gacgtagGAGAGGAa AUCCUCUC m7b Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-1236-3p gacgtaGAAGAGaggaa CCUCUUCC m6b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-155-3p gacGTAGGAGaggaa CUCCUACA m7a Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4279 gacgtAGGAGAGgaa CUCUCCUC m7a Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6845-3p gacgtAGGAGAGGaa CCUCUCCU m8a Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-7111-3p gacgtagGAGAGGAa AUCCUCUC m7b Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-1236-3p gacgtaGAAGAGaggaa CCUCUUCC m6b Disrupted HHKTA_10544_NM_005066|1791|1830|6.31711939355653|7.21304004917053
hsa-miR-155-3p gacGTAGGAGaggaa CUCCUACA m7a Created HHKTA_10544_NM_005066|1791|1830|6.31711939355653|7.21304004917053
hsa-miR-4279 gacgtAGGAGAGgaa CUCUCCUC m7a Created HHKTA_10544_NM_005066|1791|1830|6.31711939355653|7.21304004917053
hsa-miR-6845-3p gacgtAGGAGAGGaa CCUCUCCU m8a Created HHKTA_10544_NM_005066|1791|1830|6.31711939355653|7.21304004917053
hsa-miR-7111-3p gacgtagGAGAGGAa AUCCUCUC m7b Created HHKTA_10544_NM_005066|1791|1830|6.31711939355653|7.21304004917053

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35188047C>T COSM186342 TCGA-AA-3949-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-15b-3p gATGATTCGtcaacg CGAAUCAU m8a (m8a->m7a) HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-15b-3p gATGATTCGtcaacg CGAAUCAU m8a (m8a->m7a) HHHNE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-15b-3p gATGATTCGtcaacg CGAAUCAU m8a (m8a->m7a) HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-15b-3p gATGATTCGtcaacg CGAAUCAU m8a (m8a->m7a) HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-15b-3p gATGATTCGtcaacg CGAAUCAU m8a (m8a->m7a) HHHSE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-15b-3p gATGATTCGtcaacg CGAAUCAU m8a (m8a->m7a) HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-15b-3p gATGATTCGtcaacg CGAAUCAU m8a (m8a->m7a) HHKTA_20551_NM_005066|1831|1870|3.54797116624408|7.21304004917053

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35188016G>A COSM4007341 TCGA-BR-8361-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-566 atgAGGCGCCaaaga GGGCGCCU m7b Disrupted HHHNE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-668-5p atGAGGCGCcaaaga UGCGCCUC m7b (m7b->m6b) HHHNE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-6789-3p atgaGGCGCCaaaga CGGCGCCC m6b Disrupted HHHNE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-9-5p atgaggcACCAAAGa UCUUUGGU m7b Created HHHNE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-566 atgAGGCGCCaaaga GGGCGCCU m7b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-668-5p atGAGGCGCcaaaga UGCGCCUC m7b (m7b->m6b) HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6789-3p atgaGGCGCCaaaga CGGCGCCC m6b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-9-5p atgaggcACCAAAGa UCUUUGGU m7b Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-566 atgAGGCGCCaaaga GGGCGCCU m7b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-668-5p atGAGGCGCcaaaga UGCGCCUC m7b (m7b->m6b) HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6789-3p atgaGGCGCCaaaga CGGCGCCC m6b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-9-5p atgaggcACCAAAGa UCUUUGGU m7b Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-566 atgAGGCGCCaaaga GGGCGCCU m7b Disrupted HHHSE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-668-5p atGAGGCGCcaaaga UGCGCCUC m7b (m7b->m6b) HHHSE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-6789-3p atgaGGCGCCaaaga CGGCGCCC m6b Disrupted HHHSE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-9-5p atgaggcACCAAAGa UCUUUGGU m7b Created HHHSE_16523_SFPQ|NM_005066|exon_CDS|-7.32550960947095|1.62252397536141
hsa-miR-566 atgAGGCGCCaaaga GGGCGCCU m7b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-668-5p atGAGGCGCcaaaga UGCGCCUC m7b (m7b->m6b) HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6789-3p atgaGGCGCCaaaga CGGCGCCC m6b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-9-5p atgaggcACCAAAGa UCUUUGGU m7b Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-566 atgAGGCGCCaaaga GGGCGCCU m7b Disrupted HHKTA_20551_NM_005066|1831|1870|3.54797116624408|7.21304004917053
hsa-miR-668-5p atGAGGCGCcaaaga UGCGCCUC m7b (m7b->m6b) HHKTA_20551_NM_005066|1831|1870|3.54797116624408|7.21304004917053
hsa-miR-6789-3p atgaGGCGCCaaaga CGGCGCCC m6b Disrupted HHKTA_20551_NM_005066|1831|1870|3.54797116624408|7.21304004917053
hsa-miR-9-5p atgaggcACCAAAGa UCUUUGGU m7b Created HHKTA_20551_NM_005066|1831|1870|3.54797116624408|7.21304004917053
hsa-miR-566 atgAGGCGCCaaaga GGGCGCCU m7b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-668-5p atGAGGCGCcaaaga UGCGCCUC m7b (m7b->m6b) HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6789-3p atgaGGCGCCaaaga CGGCGCCC m6b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-9-5p atgaggcACCAAAGa UCUUUGGU m7b Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35188008G>C COSM164295 PD4603a [NS][NS][NS][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1238-3p ccaaagaGAGGAAag CUUCCUCG m6b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-3074-5p ccaaagaCAGGAAag GUUCCUGC m6b Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-3120-5p ccaaAGACAGGaaag CCUGUCUG m7a Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-3183 ccaaAGAGAGGaaag GCCUCUCU m7b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-4421 ccaaAGACAGGaaag ACCUGUCU m7b Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-4723-3p ccaaAGAGAGGaaag CCCUCUCU m7b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-4753-3p ccAAAGAGAggaaag UUCUCUUU m7b (m7b->m6b) HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-511-5p ccAAAGACAggaaag GUGUCUUU m7b (m6b->m7b) HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-5699-3p ccaaAGACAGGAaag UCCUGUCU m8a Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6748-3p ccaaaGACAGGAaag UCCUGUCC m7a Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6769b-3p ccaaAGAGAGGaaag CCCUCUCU m7b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6780a-3p ccaaagAGAGGAaag CUCCUCUG m6b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6881-3p ccaaagAGAGGAaag AUCCUCUU m6b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-7111-3p ccaaaGAGAGGAaag AUCCUCUC m7b Disrupted HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-7152-5p ccaaagACAGGAAAg UUUCCUGU m8a Created HHHNA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-1238-3p ccaaagaGAGGAAag CUUCCUCG m6b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-130b-5p ccAAAGAGaggaaag ACUCUUUC m6b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-3074-5p ccaaagaCAGGAAag GUUCCUGC m6b Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-3120-5p ccaaAGACAGGaaag CCUGUCUG m7a Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-3183 ccaaAGAGAGGaaag GCCUCUCU m7b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4421 ccaaAGACAGGaaag ACCUGUCU m7b Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4723-3p ccaaAGAGAGGaaag CCCUCUCU m7b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4753-3p ccAAAGAGAggaaag UUCUCUUU m7b (m7b->m6b) HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-511-5p ccAAAGACAggaaag GUGUCUUU m7b (m6b->m7b) HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-5699-3p ccaaAGACAGGAaag UCCUGUCU m8a Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6748-3p ccaaaGACAGGAaag UCCUGUCC m7a Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6769b-3p ccaaAGAGAGGaaag CCCUCUCU m7b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6780a-3p ccaaagAGAGGAaag CUCCUCUG m6b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6881-3p ccaaagAGAGGAaag AUCCUCUU m6b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-7111-3p ccaaaGAGAGGAaag AUCCUCUC m7b Disrupted HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-7152-5p ccaaagACAGGAAAg UUUCCUGU m8a Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-1238-3p ccaaagaGAGGAAag CUUCCUCG m6b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-130b-5p ccAAAGAGaggaaag ACUCUUUC m6b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-3074-5p ccaaagaCAGGAAag GUUCCUGC m6b Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-3120-5p ccaaAGACAGGaaag CCUGUCUG m7a Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-3183 ccaaAGAGAGGaaag GCCUCUCU m7b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-4421 ccaaAGACAGGaaag ACCUGUCU m7b Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-4723-3p ccaaAGAGAGGaaag CCCUCUCU m7b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-4753-3p ccAAAGAGAggaaag UUCUCUUU m7b (m7b->m6b) HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-511-5p ccAAAGACAggaaag GUGUCUUU m7b (m6b->m7b) HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-5699-3p ccaaAGACAGGAaag UCCUGUCU m8a Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6748-3p ccaaaGACAGGAaag UCCUGUCC m7a Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6769b-3p ccaaAGAGAGGaaag CCCUCUCU m7b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6780a-3p ccaaagAGAGGAaag CUCCUCUG m6b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-6881-3p ccaaagAGAGGAaag AUCCUCUU m6b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-7111-3p ccaaaGAGAGGAaag AUCCUCUC m7b Disrupted HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-7152-5p ccaaagACAGGAAAg UUUCCUGU m8a Created HHHSA_676_SFPQ|NM_005066|exon_CDS|-7.73195430127093|-0.211619248731406
hsa-miR-1238-3p ccaaagaGAGGAAag CUUCCUCG m6b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-130b-5p ccAAAGAGaggaaag ACUCUUUC m6b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-3074-5p ccaaagaCAGGAAag GUUCCUGC m6b Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-3120-5p ccaaAGACAGGaaag CCUGUCUG m7a Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-3183 ccaaAGAGAGGaaag GCCUCUCU m7b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4421 ccaaAGACAGGaaag ACCUGUCU m7b Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4723-3p ccaaAGAGAGGaaag CCCUCUCU m7b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4753-3p ccAAAGAGAggaaag UUCUCUUU m7b (m7b->m6b) HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-511-5p ccAAAGACAggaaag GUGUCUUU m7b (m6b->m7b) HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-5699-3p ccaaAGACAGGAaag UCCUGUCU m8a Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6748-3p ccaaaGACAGGAaag UCCUGUCC m7a Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6769b-3p ccaaAGAGAGGaaag CCCUCUCU m7b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6780a-3p ccaaagAGAGGAaag CUCCUCUG m6b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6881-3p ccaaagAGAGGAaag AUCCUCUU m6b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-7111-3p ccaaaGAGAGGAaag AUCCUCUC m7b Disrupted HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-7152-5p ccaaagACAGGAAAg UUUCCUGU m8a Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187992G>A COSM167615 TCGA-AG-A002-01 [large_intestine][rectum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4687-3p tACAGCCAaatgggc UGGCUGUU m7a Created HHHNA_675_SFPQ|NM_005066|exon_CDS|-8.29136414452522|0.718563733101108
hsa-miR-647 taCAGCCAaatgggc GUGGCUGC m6b Created HHHNA_675_SFPQ|NM_005066|exon_CDS|-8.29136414452522|0.718563733101108
hsa-miR-6842-3p taCAGCCAAatgggc UUGGCUGG m7a (m6a->m7a) HHHNA_675_SFPQ|NM_005066|exon_CDS|-8.29136414452522|0.718563733101108
hsa-miR-4687-3p tACAGCCAaatgggc UGGCUGUU m7a Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-647 taCAGCCAaatgggc GUGGCUGC m6b Created HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6842-3p taCAGCCAAatgggc UUGGCUGG m7a (m6a->m7a) HHHNH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4687-3p tACAGCCAaatgggc UGGCUGUU m7a Created HHHSA_675_SFPQ|NM_005066|exon_CDS|-8.29136414452522|0.718563733101108
hsa-miR-647 taCAGCCAaatgggc GUGGCUGC m6b Created HHHSA_675_SFPQ|NM_005066|exon_CDS|-8.29136414452522|0.718563733101108
hsa-miR-6842-3p taCAGCCAAatgggc UUGGCUGG m7a (m6a->m7a) HHHSA_675_SFPQ|NM_005066|exon_CDS|-8.29136414452522|0.718563733101108
hsa-miR-4687-3p tACAGCCAaatgggc UGGCUGUU m7a Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-647 taCAGCCAaatgggc GUGGCUGC m6b Created HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-6842-3p taCAGCCAAatgggc UUGGCUGG m7a (m6a->m7a) HHHSH_3372_SFPQ|NM_005066|exon_CDS|-9.15974704211505|0.421199858315141
hsa-miR-4687-3p tACAGCCAaatgggc UGGCUGUU m7a Created HPRO6_5909_G6875.1_35653592
hsa-miR-647 taCAGCCAaatgggc GUGGCUGC m6b Created HPRO6_5909_G6875.1_35653592
hsa-miR-6842-3p taCAGCCAAatgggc UUGGCUGG m7a (m6a->m7a) HPRO6_5909_G6875.1_35653592
hsa-miR-4687-3p tACAGCCAaatgggc UGGCUGUU m7a Created HPTA3_1439_G2221.1_35653592
hsa-miR-647 taCAGCCAaatgggc GUGGCUGC m6b Created HPTA3_1439_G2221.1_35653592
hsa-miR-6842-3p taCAGCCAAatgggc UUGGCUGG m7a (m6a->m7a) HPTA3_1439_G2221.1_35653592
hsa-miR-4687-3p tACAGCCAaatgggc UGGCUGUU m7a Created HPTK1_2272_G2688.1_35653592
hsa-miR-647 taCAGCCAaatgggc GUGGCUGC m6b Created HPTK1_2272_G2688.1_35653592
hsa-miR-6842-3p taCAGCCAAatgggc UUGGCUGG m7a (m6a->m7a) HPTK1_2272_G2688.1_35653592

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187236C>T COSM4007340 TCGA-CD-8536-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-23a-3p agacATGTGAatggg AUCACAUU m6b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-23b-3p agacATGTGAatggg AUCACAUU m6b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-23c agacATGTGAatggg AUCACAUU m6b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4717-3p agaCATGTGaatggg ACACAUGG m6b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-23a-3p agacATGTGAatggg AUCACAUU m6b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-23b-3p agacATGTGAatggg AUCACAUU m6b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-23c agacATGTGAatggg AUCACAUU m6b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4717-3p agaCATGTGaatggg ACACAUGG m6b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187235G>A COSM277250 TCGA-AA-A00N-01 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3680-3p gacATGCAAAtgggt UUUUGCAU m7b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4666b gACATGCAAatgggt UUGCAUGU m8a (m7a->m8a) HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-5011-3p gaCATGCAaatgggt GUGCAUGG m6b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-3680-3p gacATGCAAAtgggt UUUUGCAU m7b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4666b gACATGCAAatgggt UUGCAUGU m8a (m7a->m8a) HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-5011-3p gaCATGCAaatgggt GUGCAUGG m6b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187225C>T COSM247277 TCGA-AP-A0LM-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4691-5p tgggtggTGGAGGAg GUCCUCCA m7b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-6084 tgggTGGCGGAggag UUCCGCCA m7b Disrupted HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-6792-3p tgggtggTGGAGGAg CUCCUCCA m7b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4691-5p tgggtggTGGAGGAg GUCCUCCA m7b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-6084 tgggTGGCGGAggag UUCCGCCA m7b Disrupted HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-6792-3p tgggtggTGGAGGAg CUCCUCCA m7b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187224G>A COSM908657 TCGA-BS-A0UF-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4715-3p gGGTGGCAgaggagc GUGCCACC m7b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4727-5p gggTGGCAGAggagc AUCUGCCA m7b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-6084 gggTGGCGGAggagc UUCCGCCA m7b Disrupted HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-6780a-3p gggtggCAGAGGAGc CUCCUCUG m8a Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4715-3p gGGTGGCAgaggagc GUGCCACC m7b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4727-5p gggTGGCAGAggagc AUCUGCCA m7b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-6084 gggTGGCGGAggagc UUCCGCCA m7b Disrupted HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-6780a-3p gggtggCAGAGGAGc CUCCUCUG m8a Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187206G>T COSM534783 TCGA-38-4632-01 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2116-3p gaacATGGGAGGtaa CCUCCCAU m8a Disrupted HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4717-3p gaaCATGTGaggtaa ACACAUGG m6b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4777-3p gaacatgTGAGGTAa AUACCUCA m7b Created HHHSA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-2116-3p gaacATGGGAGGtaa CCUCCCAU m8a Disrupted HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4717-3p gaaCATGTGaggtaa ACACAUGG m6b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711
hsa-miR-4777-3p gaacatgTGAGGTAa AUACCUCA m7b Created HHHNA_674_SFPQ|NM_005066|exon_CDS|-7.40667243095438|0.0960414503645711

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187089C>A COSM1166699 ID15 [haematopoietic_and_lymphoid_tissue][NS][haematopoietic_neoplasm][acute_myeloid_leukaemia]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4491 ttTCCACATctagga AAUGUGGA m7b (m6b->m7b) HHFCT_1702_cluster-1430_10_157
hsa-miR-4657 ttTCCACATctagga AAUGUGGA m7b (m6b->m7b) HHFCT_1702_cluster-1430_10_157
hsa-miR-520g-5p tttccaCCTCTAGga UCUAGAGG m7b Disrupted HHFCT_1702_cluster-1430_10_157
hsa-miR-576-3p tttcCACATCTagga AAGAUGUG m7b Created HHFCT_1702_cluster-1430_10_157
hsa-miR-6134 tttCCACCTCtagga UGAGGUGG m7b Disrupted HHFCT_1702_cluster-1430_10_157
hsa-miR-6833-5p tTTCCACAtctagga GUGUGGAA m7b Created HHFCT_1702_cluster-1430_10_157
hsa-miR-4491 ttTCCACATctagga AAUGUGGA m7b (m6b->m7b) HHFKP_1606_cluster-1430_14_190
hsa-miR-4657 ttTCCACATctagga AAUGUGGA m7b (m6b->m7b) HHFKP_1606_cluster-1430_14_190
hsa-miR-520g-5p tttccaCCTCTAGga UCUAGAGG m7b Disrupted HHFKP_1606_cluster-1430_14_190
hsa-miR-576-3p tttcCACATCTagga AAGAUGUG m7b Created HHFKP_1606_cluster-1430_14_190
hsa-miR-6134 tttCCACCTCtagga UGAGGUGG m7b Disrupted HHFKP_1606_cluster-1430_14_190
hsa-miR-6833-5p tTTCCACAtctagga GUGUGGAA m7b Created HHFKP_1606_cluster-1430_14_190

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187079AGGT>T COSM908656 TCGA-B5-A11H-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1306-5p ctctaGGAGGTGGtggtg CCACCUCC m8a Disrupted HHFCT_1702_cluster-1430_10_157
hsa-miR-1306-5p ctctaGGAGGTGGtggtg CCACCUCC m8a Disrupted HHFKP_1606_cluster-1430_14_190
Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187066G>C COSM4399391 TCGA-BF-A1PZ-01 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187048G>T COSM534784 TCGA-50-5931-01 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-541-5p tAATCCTTgcgttcc AAAGGAUU m7b Created HHFCT_1702_cluster-1430_10_157
hsa-miR-541-5p tAATCCTTgcgttcc AAAGGAUU m7b Created HHFKP_1606_cluster-1430_14_190
hsa-miR-541-5p tAATCCTTgcgttcc AAAGGAUU m7b Created HHHNE_16522_SFPQ|NM_005066|exon_CDS|-8.4089134750035|-0.10260232222441
hsa-miR-541-5p tAATCCTTgcgttcc AAAGGAUU m7b Created HHHSE_16522_SFPQ|NM_005066|exon_CDS|-8.4089134750035|-0.10260232222441
hsa-miR-541-5p tAATCCTTgcgttcc AAAGGAUU m7b Created HPRO6_5908_G6874.1_35652650
Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187047G>A COSM284935 TCGA-AA-A010-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
No TargetScan sites are altered. To display all potentially impacted target sites, select "All 6mer or longer seed matches" above.


Mutation Mutation ID Sample Name Cancer Type
chr1:g.35187031C>T COSM3865452 TCGA-FW-A3R5-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-218-2-3p cagcAACCATGagtg CAUGGUUC m7a Disrupted HHHNE_16522_SFPQ|NM_005066|exon_CDS|-8.4089134750035|-0.10260232222441
hsa-miR-758-5p cagCAACCATgagtg GAUGGUUG m7b Disrupted HHHNE_16522_SFPQ|NM_005066|exon_CDS|-8.4089134750035|-0.10260232222441
hsa-miR-218-2-3p cagcAACCATGagtg CAUGGUUC m7a Disrupted HHHSE_16522_SFPQ|NM_005066|exon_CDS|-8.4089134750035|-0.10260232222441
hsa-miR-758-5p cagCAACCATgagtg GAUGGUUG m7b Disrupted HHHSE_16522_SFPQ|NM_005066|exon_CDS|-8.4089134750035|-0.10260232222441

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35184565C>T COSM1342123 TCGA-BR-7851-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1228-3p ggAGGTGTGgggcct UCACACCU m7b (m6b->m7b) HHHNA_673_SFPQ|NM_005066|exon_CDS|-6.54329318789797|0.460768737425992
hsa-miR-4758-3p ggaggtGTGGGGCct UGCCCCAC m7b Created HHHNA_673_SFPQ|NM_005066|exon_CDS|-6.54329318789797|0.460768737425992
hsa-miR-874-5p ggaggtgTGGGGCCt CGGCCCCA m7b Created HHHNA_673_SFPQ|NM_005066|exon_CDS|-6.54329318789797|0.460768737425992
hsa-miR-1228-3p ggAGGTGTGgggcct UCACACCU m7b (m6b->m7b) HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-4758-3p ggaggtGTGGGGCct UGCCCCAC m7b Created HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-874-5p ggaggtgTGGGGCCt CGGCCCCA m7b Created HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-1228-3p ggAGGTGTGgggcct UCACACCU m7b (m6b->m7b) HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-4758-3p ggaggtGTGGGGCct UGCCCCAC m7b Created HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-874-5p ggaggtgTGGGGCCt CGGCCCCA m7b Created HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-1228-3p ggAGGTGTGgggcct UCACACCU m7b (m6b->m7b) HHHSA_673_SFPQ|NM_005066|exon_CDS|-6.54329318789797|0.460768737425992
hsa-miR-4758-3p ggaggtGTGGGGCct UGCCCCAC m7b Created HHHSA_673_SFPQ|NM_005066|exon_CDS|-6.54329318789797|0.460768737425992
hsa-miR-874-5p ggaggtgTGGGGCCt CGGCCCCA m7b Created HHHSA_673_SFPQ|NM_005066|exon_CDS|-6.54329318789797|0.460768737425992
hsa-miR-1228-3p ggAGGTGTGgggcct UCACACCU m7b (m6b->m7b) HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-4758-3p ggaggtGTGGGGCct UGCCCCAC m7b Created HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-874-5p ggaggtgTGGGGCCt CGGCCCCA m7b Created HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-1228-3p ggAGGTGTGgggcct UCACACCU m7b (m6b->m7b) HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-4758-3p ggaggtGTGGGGCct UGCCCCAC m7b Created HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-874-5p ggaggtgTGGGGCCt CGGCCCCA m7b Created HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076

Mutation Mutation ID Sample Name Cancer Type
chr1:g.35184564G>T COSM4127671 SS6003305 [oesophagus][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3065-3p gaGGTGCTGggcctg UCAGCACC m7b (m6b->m7b) HHHSA_673_SFPQ|NM_005066|exon_CDS|-6.54329318789797|0.460768737425992
hsa-miR-3065-3p gaGGTGCTGggcctg UCAGCACC m7b (m6b->m7b) HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-3065-3p gaGGTGCTGggcctg UCAGCACC m7b (m6b->m7b) HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-3065-3p gaGGTGCTGggcctg UCAGCACC m7b (m6b->m7b) HHHNA_673_SFPQ|NM_005066|exon_CDS|-6.54329318789797|0.460768737425992
hsa-miR-3065-3p gaGGTGCTGggcctg UCAGCACC m7b (m6b->m7b) HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-3065-3p gaGGTGCTGggcctg UCAGCACC m7b (m6b->m7b) HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
Mutation Mutation ID Sample Name Cancer Type
chr1:g.35184552T>G COSM3805032 TCGA-A8-A0A6-01 [breast][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.


Mutation Mutation ID Sample Name Cancer Type
chr1:g.35184516A>G COSM908655 TCGA-AP-A059-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHNA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHNA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHNA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHNA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHNA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHNA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHNA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHNA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHNA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHNA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHNE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHNE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHNE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHNE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHNE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHNE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHNH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHNH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHNH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHNH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHNH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHNH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHSA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHSA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHSA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHSA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHSA_671_SFPQ|NM_005066|exon_CDS|-6.27188767945231|0.765521241721138
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHSA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHSA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHSA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHSA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHSA_672_SFPQ|NM_005066|exon_CDS|-6.60922516867222|0.661770100226619
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHSE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHSE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHSE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHSE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHSE_16520_SFPQ|NM_005066|exon_CDS|-6.57161637042684|0.590411990547079
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHSE_16521_SFPQ|NM_005066|exon_CDS|-6.06236829702009|0.437932246124968
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHSH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHSH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHSH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHSH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHSH_3370_SFPQ|NM_005066|exon_CDS|-9.30061676954599|-1.03000021733927
hsa-miR-3135b gaaCTCCAGCaggat GGCUGGAG m7b Disrupted HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-3692-5p gaactCCAGCAGGat CCUGCUGG m8a Disrupted HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-370-3p gaactcCAGCAGGat GCCUGCUG m7b Disrupted HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-4722-3p gaactccGGCAGGat ACCUGCCA m6b Created HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076
hsa-miR-6893-3p gaactcCAGCAGGat CCCUGCUG m7b Disrupted HHHSH_3371_SFPQ|NM_005066|exon_CDS|-8.94104707769844|-0.260070476622076

*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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