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_006988
Gene Symbol: ADAMTS1
Browse Associations

Somatic mutations that impact miRNA target sites


Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844571C>T COSM4659432 T2284 [large_intestine][rectum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-128-3p ccggCACTGTGAatg UCACAGUG m8a Created HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-216a-3p ccggCACTGTGAatg UCACAGUG m8a Created HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-27a-3p ccggcACTGTGAAtg UUCACAGU m8a Created HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-27b-3p ccggcACTGTGAAtg UUCACAGU m8a Created HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-3681-3p ccggCACTGTGaatg ACACAGUG m7b Created HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-371a-3p cCGGCACTgtgaatg AAGUGCCG m7b Created HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-128-3p ccggCACTGTGAatg UCACAGUG m8a Created HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-216a-3p ccggCACTGTGAatg UCACAGUG m8a Created HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-27a-3p ccggcACTGTGAAtg UUCACAGU m8a Created HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-27b-3p ccggcACTGTGAAtg UUCACAGU m8a Created HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-3681-3p ccggCACTGTGaatg ACACAGUG m7b Created HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-371a-3p cCGGCACTgtgaatg AAGUGCCG m7b Created HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844550G>A COSM4659431 T36 [kidney][NS][carcinoma][clear_cell_renal_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4663 ccaGCTCAGCTgccg AGCUGAGC m8a Created HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-4663 ccaGCTCAGCTgccg AGCUGAGC m8a Created HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844540C>G COSM4646269 LS180 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-7160-5p tgccgcCCTCAGCct UGCUGAGG m7b Disrupted HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-1226-5p tgccGCCCTCAgcct GUGAGGGC m7b Disrupted HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-3141 tgCCGCCCTCagcct GAGGGCGG m8a Disrupted HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-3616-3p tgccGCCCTCagcct CGAGGGCA m6b Disrupted HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-7160-5p tgccgcCCTCAGCct UGCUGAGG m7b Disrupted HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-1226-5p tgccGCCCTCAgcct GUGAGGGC m7b Disrupted HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-3141 tgCCGCCCTCagcct GAGGGCGG m8a Disrupted HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-3616-3p tgccGCCCTCagcct CGAGGGCA m6b Disrupted HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844532C>T COSM4100965 TCGA-BR-A4PD-01 [stomach][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2467-3p tcagCCTCTGCgagg AGCAGAGG m7b Disrupted HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-3929 TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-4419b TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-4478 TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-485-5p tCAGCCTCTgcgagg AGAGGCUG m8a (m8a->m7a) HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-6884-5p tCAGCCTCTgcgagg AGAGGCUG m8a (m8a->m7a) HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-2467-3p tcagCCTCTGCgagg AGCAGAGG m7b Disrupted HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-3929 TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-4419b TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-4478 TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-485-5p tCAGCCTCTgcgagg AGAGGCUG m8a (m8a->m7a) HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-6884-5p tCAGCCTCTgcgagg AGAGGCUG m8a (m8a->m7a) HHHNE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-2467-3p tcagCCTCTGCgagg AGCAGAGG m7b Disrupted HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-3929 TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-4419b TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-4478 TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-485-5p tCAGCCTCTgcgagg AGAGGCUG m8a (m8a->m7a) HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-6884-5p tCAGCCTCTgcgagg AGAGGCUG m8a (m8a->m7a) HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-2467-3p tcagCCTCTGCgagg AGCAGAGG m7b Disrupted HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-3929 TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-4419b TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-4478 TCAGCCTCtgcgagg GAGGCUGA m8a Disrupted HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-485-5p tCAGCCTCTgcgagg AGAGGCUG m8a (m8a->m7a) HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575
hsa-miR-6884-5p tCAGCCTCTgcgagg AGAGGCUG m8a (m8a->m7a) HHHSE_336_ADAMTS1|NM_006988|exon_CDS|-7.55546427916594|-0.247819629152575

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844523C>T COSM4624365 DLD1 [large_intestine][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6865-3p gcGAGGGTGTgcgcg ACACCCUC m8a Created HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-6865-3p gcGAGGGTGTgcgcg ACACCCUC m8a Created HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844522G>A COSM1413518 T3116 [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
chr21:g.26844493G>T COSM4646654 LS411 [large_intestine][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1281 tgggGGAGGCGtatt UCGCCUCC m7b Disrupted HHHNA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-324-5p tggGGGATGCGtatt CGCAUCCC m8a Created HHHNA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-6729-3p tgGGGGATGcgtatt UCAUCCCC m7b (m6b->m7b) HHHNA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-6778-3p tggGGGAGGCgtatt UGCCUCCC m7b Disrupted HHHNA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-1281 tgggGGAGGCGtatt UCGCCUCC m7b Disrupted HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-324-5p tggGGGATGCGtatt CGCAUCCC m8a Created HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-6729-3p tgGGGGATGcgtatt UCAUCCCC m7b (m6b->m7b) HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-6778-3p tggGGGAGGCgtatt UGCCUCCC m7b Disrupted HHHNE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-1281 tgggGGAGGCGtatt UCGCCUCC m7b Disrupted HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-324-5p tggGGGATGCGtatt CGCAUCCC m8a Created HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-6729-3p tgGGGGATGcgtatt UCAUCCCC m7b (m6b->m7b) HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-6778-3p tggGGGAGGCgtatt UGCCUCCC m7b Disrupted HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-1281 tgggGGAGGCGtatt UCGCCUCC m7b Disrupted HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-324-5p tggGGGATGCGtatt CGCAUCCC m8a Created HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-6729-3p tgGGGGATGcgtatt UCAUCCCC m7b (m6b->m7b) HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716
hsa-miR-6778-3p tggGGGAGGCgtatt UGCCUCCC m7b Disrupted HHHSE_335_ADAMTS1|NM_006988|exon_CDS|-7.93501268685064|0.0523159992979716

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844478G>A COSM3668510 CHC465T [liver][NS][carcinoma][hepatocellular_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1287-5p tcATCCAGCcgctgc UGCUGGAU m7b (m7b->m6b) HHHNA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-3652 tcaTCCAGCCGctgc CGGCUGGA m8a Disrupted HHHNA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-4430 tcaTCCAGCCgctgc AGGCUGGA m7b Disrupted HHHNA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-1287-5p tcATCCAGCcgctgc UGCUGGAU m7b (m7b->m6b) HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-3652 tcaTCCAGCCGctgc CGGCUGGA m8a Disrupted HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-4430 tcaTCCAGCCgctgc AGGCUGGA m7b Disrupted HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844451C>A COSM22809 NCI-H2009 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6069 agcgCCTAGCCaccg GGGCUAGG m7b Created HHHNA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-3197 aGCGCCTCgccaccg GGAGGCGC m7b Disrupted HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438
hsa-miR-6069 agcgCCTAGCCaccg GGGCUAGG m7b Created HHHSA_15104_ADAMTS1|NM_006988|exon_CDS|-7.72814104081767|-1.50852163554438

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844402C>G COSM116488 TCGA-25-2042-01 [ovary][NS][carcinoma][serous_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1286 gttccacGTCCTGCg UGCAGGAC m7b Created HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-3689d gttcCACCTCCtgcg GGGAGGUG m7b Disrupted HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-4459 gttccaCCTCCTGcg CCAGGAGG m7b Disrupted HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-4722-5p gttccacCTCCTGCg GGCAGGAG m7b Disrupted HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6134 gttCCACCTCctgcg UGAGGUGG m7b Disrupted HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6851-5p gttcCACCTCCTgcg AGGAGGUG m8a Disrupted HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-1286 gttccacGTCCTGCg UGCAGGAC m7b Created HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-3689d gttcCACCTCCtgcg GGGAGGUG m7b Disrupted HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-4459 gttccaCCTCCTGcg CCAGGAGG m7b Disrupted HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-4722-5p gttccacCTCCTGCg GGCAGGAG m7b Disrupted HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6134 gttCCACCTCctgcg UGAGGUGG m7b Disrupted HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6851-5p gttcCACCTCCTgcg AGGAGGUG m8a Disrupted HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844387C>T COSM1181826 587376 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-192-3p gcggaATTGGCAGgg CUGCCAAU m8a Created HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-4722-3p gcggaatTGGCAGGg ACCUGCCA m7b Created HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6727-3p gcggaatTGGCAGGg UCCUGCCA m7b Created HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-192-3p gcggaATTGGCAGgg CUGCCAAU m8a Created HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-4722-3p gcggaatTGGCAGGg ACCUGCCA m7b Created HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6727-3p gcggaatTGGCAGGg UCCUGCCA m7b Created HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844378G>A COSM4627870 Gp5D [large_intestine][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1181 gcagGGCGACGtcgg CCGUCGCC m7b Disrupted HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6726-3p gcAGGGCGAcgtcgg CUCGCCCU m7b (m7b->m6b) HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6799-3p GCAGGGCAacgtcgg UGCCCUGC m8a Created HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-7976 gCAGGGCAacgtcgg UGCCCUGA m7a Created HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-874-3p gCAGGGCAacgtcgg CUGCCCUG m7b Created HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-1181 gcagGGCGACGtcgg CCGUCGCC m7b Disrupted HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6726-3p gcAGGGCGAcgtcgg CUCGCCCU m7b (m7b->m6b) HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6799-3p GCAGGGCAacgtcgg UGCCCUGC m8a Created HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-7976 gCAGGGCAacgtcgg UGCCCUGA m7a Created HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-874-3p gCAGGGCAacgtcgg CUGCCCUG m7b Created HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844373C>A COSM3758814 TCGA-G4-6321-01 [large_intestine][caecum][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
chr21:g.26844365C>T COSM296444 TCGA-AA-3877-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-5589-3p ggcggCATGTGCggg UGCACAUG m7b Created HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6767-3p ggcgGCACGTGcggg CCACGUGC m7b Disrupted HHHNA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-5589-3p ggcggCATGTGCggg UGCACAUG m7b Created HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
hsa-miR-6767-3p ggcgGCACGTGcggg CCACGUGC m7b Disrupted HHHSA_15103_ADAMTS1|NM_006988|exon_CDS|-7.35246359028134|-0.79154669088431
Mutation Mutation ID Sample Name Cancer Type
chr21:g.26844355C>G COSM3758813 TCGA-D5-6537-01 [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
chr21:g.26844347A>G COSM4659430 T2940 [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
chr21:g.26838268C>A COSM444316 TCGA-AX-A05Z-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-144-5p tgGATATCatgatat GGAUAUCA m6b Disrupted HHKTA_46315_NM_006988|2670|2709|1.55764587786326|2.2823351383058
hsa-miR-382-3p tggatatAATGATat AAUCAUUC m6b Created HHKTA_46315_NM_006988|2670|2709|1.55764587786326|2.2823351383058
hsa-miR-433-3p tggatATCATGATat AUCAUGAU m8a Disrupted HHKTA_46315_NM_006988|2670|2709|1.55764587786326|2.2823351383058
hsa-miR-4528 tggaTATAATGAtat UCAUUAUA m8a Created HHKTA_46315_NM_006988|2670|2709|1.55764587786326|2.2823351383058
hsa-miR-6083 tgGATATAAtgatat CUUAUAUC m7b (m6b->m7b) HHKTA_46315_NM_006988|2670|2709|1.55764587786326|2.2823351383058
hsa-miR-96-3p tggatatCATGATat AAUCAUGU m6b Disrupted HHKTA_46315_NM_006988|2670|2709|1.55764587786326|2.2823351383058

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26838180T>G COSM4751746 pfg120T [stomach][NS][carcinoma][intestinal_adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-183-5p agctttcGTGCCATc UAUGGCAC m7b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-31-5p agcttTCTTGCCatc AGGCAAGA m7b Disrupted HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-564 agctttCGTGCCatc AGGCACGG m6b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-183-5p agctttcGTGCCATc UAUGGCAC m7b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-31-5p agcttTCTTGCCatc AGGCAAGA m7b Disrupted HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-564 agctttCGTGCCatc AGGCACGG m6b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26838177C>T COSM1632439 RK065_C01 [liver][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-31-5p ttTCTTGCCatcaaa AGGCAAGA m7b (m7b->m6b) HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-31-5p ttTCTTGCCatcaaa AGGCAAGA m7b (m7b->m6b) HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26838170A>C COSM1181824 587342 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-503-5p ccatcaaCGCTGCTg UAGCAGCG m7b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-646 ccatcaaAGCTGCTg AAGCAGCU m7b Disrupted HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-503-5p ccatcaaCGCTGCTg UAGCAGCG m7b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-646 ccatcaaAGCTGCTg AAGCAGCU m7b Disrupted HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26838169G>C COSM1578707 MN-290 [meninges][NS][meningioma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-214-3p catcaaaCCTGCTGa ACAGCAGG m7b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-3619-5p catcaaaCCTGCTGa UCAGCAGG m7b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-424-5p catcaaaGCTGCTGa CAGCAGCA m7a Disrupted HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-4464 catCAAACCTgctga AAGGUUUG m7b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-4748 catCAAACCTgctga GAGGUUUG m7b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-497-5p catcaaaGCTGCTGa CAGCAGCA m7a Disrupted HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-6165 catcaaaCCTGCTGa CAGCAGGA m7a Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-646 catcaaAGCTGCTga AAGCAGCU m7b Disrupted HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-6510-5p catcaaaCCTGCTGa CAGCAGGG m7a Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-657 catcaAACCTGCtga GGCAGGUU m7b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-761 catcaaaCCTGCTGa GCAGCAGG m7b Created HHHNE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-214-3p catcaaaCCTGCTGa ACAGCAGG m7b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-3619-5p catcaaaCCTGCTGa UCAGCAGG m7b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-424-5p catcaaaGCTGCTGa CAGCAGCA m7a Disrupted HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-4464 catCAAACCTgctga AAGGUUUG m7b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-4748 catCAAACCTgctga GAGGUUUG m7b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-497-5p catcaaaGCTGCTGa CAGCAGCA m7a Disrupted HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-6165 catcaaaCCTGCTGa CAGCAGGA m7a Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-646 catcaaAGCTGCTga AAGCAGCU m7b Disrupted HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-6510-5p catcaaaCCTGCTGa CAGCAGGG m7a Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-657 catcaAACCTGCtga GGCAGGUU m7b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796
hsa-miR-761 catcaaaCCTGCTGa GCAGCAGG m7b Created HHHSE_323_ADAMTS1|NM_006988|exon_CDS|-8.3427984121897|0.250842672511796

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26838148C>T COSM4479541 CSCC-44-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3653-3p atataTTCTTAatgg CUAAGAAG m6b Disrupted HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-3658 atataTTCTTAAtgg UUUAAGAA m7b Disrupted HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-548c-3p atatATTTTTaatgg CAAAAAUC m6b Created HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-6507-5p ataTATTCTTaatgg GAAGAAUA m7b Disrupted HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26838123C>A COSM1534471 TCGA-69-7979-01 [lung][right_upper_lobe][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-382-5p ttgtcCAACTTagag GAAGUUGU m6b Created HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-4520-2-3p tTGTCCAActtagag UUUGGACA m7b Created HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-4521 ttgtccaCCTTAGag GCUAAGGA m6b Disrupted HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-4715-5p ttgtCCAACTTagag AAGUUGGC m7a Created HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-4735-3p ttgtcCACCTTagag AAAGGUGC m6b Disrupted HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-495-5p ttgtcCAACTTagag GAAGUUGC m6b Created HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-8071 ttGTCCACCttagag CGGUGGAC m7b (m7b->m6b) HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-382-5p ttgtcCAACTTagag GAAGUUGU m6b Created HPKTA_39552_G42541.1_28210445
hsa-miR-4520-2-3p tTGTCCAActtagag UUUGGACA m7b Created HPKTA_39552_G42541.1_28210445
hsa-miR-4521 ttgtccaCCTTAGag GCUAAGGA m6b Disrupted HPKTA_39552_G42541.1_28210445
hsa-miR-4715-5p ttgtCCAACTTagag AAGUUGGC m7a Created HPKTA_39552_G42541.1_28210445
hsa-miR-4735-3p ttgtcCACCTTagag AAAGGUGC m6b Disrupted HPKTA_39552_G42541.1_28210445
hsa-miR-495-5p ttgtcCAACTTagag GAAGUUGC m6b Created HPKTA_39552_G42541.1_28210445
hsa-miR-8071 ttGTCCACCttagag CGGUGGAC m7b (m7b->m6b) HPKTA_39552_G42541.1_28210445
hsa-miR-382-5p ttgtcCAACTTagag GAAGUUGU m6b Created HPRO6_50763_G60157.1_28210445
hsa-miR-4520-2-3p tTGTCCAActtagag UUUGGACA m7b Created HPRO6_50763_G60157.1_28210445
hsa-miR-4521 ttgtccaCCTTAGag GCUAAGGA m6b Disrupted HPRO6_50763_G60157.1_28210445
hsa-miR-4715-5p ttgtCCAACTTagag AAGUUGGC m7a Created HPRO6_50763_G60157.1_28210445
hsa-miR-4735-3p ttgtcCACCTTagag AAAGGUGC m6b Disrupted HPRO6_50763_G60157.1_28210445
hsa-miR-495-5p ttgtcCAACTTagag GAAGUUGC m6b Created HPRO6_50763_G60157.1_28210445
hsa-miR-8071 ttGTCCACCttagag CGGUGGAC m7b (m7b->m6b) HPRO6_50763_G60157.1_28210445

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26838118G>C COSM3550014 TCGA-FS-A1ZK-06 [skin][NS][malignant_melanoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1301-5p cacctTAGAGCaaga CGCUCUAG m6b Disrupted HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-1537-5p caccTTACAGCaaga AGCUGUAA m7b Created HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-4521 caCCTTAGagcaaga GCUAAGGA m6b Disrupted HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-4718 cacctTACAGCaaga AGCUGUAC m6b Created HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-4999-5p cacctTACAGCAaga UGCUGUAU m7a Created HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-6502-5p cacctTAGAGCaaga AGCUCUAG m6b Disrupted HHKTA_33736_NM_006988|2780|2819|2.20666499363961|2.2823351383058
hsa-miR-1301-5p cacctTAGAGCaaga CGCUCUAG m6b Disrupted HPKTA_39552_G42541.1_28210445
hsa-miR-1537-5p caccTTACAGCaaga AGCUGUAA m7b Created HPKTA_39552_G42541.1_28210445
hsa-miR-4521 caCCTTAGagcaaga GCUAAGGA m6b Disrupted HPKTA_39552_G42541.1_28210445
hsa-miR-4718 cacctTACAGCaaga AGCUGUAC m6b Created HPKTA_39552_G42541.1_28210445
hsa-miR-4999-5p cacctTACAGCAaga UGCUGUAU m7a Created HPKTA_39552_G42541.1_28210445
hsa-miR-6502-5p cacctTAGAGCaaga AGCUCUAG m6b Disrupted HPKTA_39552_G42541.1_28210445
hsa-miR-1301-5p cacctTAGAGCaaga CGCUCUAG m6b Disrupted HPRO6_50763_G60157.1_28210445
hsa-miR-1537-5p caccTTACAGCaaga AGCUGUAA m7b Created HPRO6_50763_G60157.1_28210445
hsa-miR-4521 caCCTTAGagcaaga GCUAAGGA m6b Disrupted HPRO6_50763_G60157.1_28210445
hsa-miR-4718 cacctTACAGCaaga AGCUGUAC m6b Created HPRO6_50763_G60157.1_28210445
hsa-miR-4999-5p cacctTACAGCAaga UGCUGUAU m7a Created HPRO6_50763_G60157.1_28210445
hsa-miR-6502-5p cacctTAGAGCaaga AGCUCUAG m6b Disrupted HPRO6_50763_G60157.1_28210445
Mutation Mutation ID Sample Name Cancer Type
chr21:g.26838052A>T COSM1029664 TCGA-AP-A054-01 [endometrium][NS][carcinoma][endometrioid_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
chr21:g.26838049C>T COSM578768 TCGA-AZ-4681-01 [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
chr21:g.26837963C>T COSM40861 Br27P [central_nervous_system][brain][glioma][astrocytoma_Grade_IV]
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
chr21:g.26837960C>T COSM4659424 T578 [large_intestine][caecum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3973 ccTACTTTGTaaaga ACAAAGUA m8a Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-520d-5p cctaCTTTGTAaaga CUACAAAG m7b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-520g-3p cctACTTTGTaaaga ACAAAGUG m7a Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-520h cctACTTTGTaaaga ACAAAGUG m7a Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-524-5p cctaCTTTGTAaaga CUACAAAG m7b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-3973 ccTACTTTGTaaaga ACAAAGUA m8a Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-520d-5p cctaCTTTGTAaaga CUACAAAG m7b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-520g-3p cctACTTTGTaaaga ACAAAGUG m7a Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-520h cctACTTTGTaaaga ACAAAGUG m7a Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-524-5p cctaCTTTGTAaaga CUACAAAG m7b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837954G>A COSM4538287 CSCC-31-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-2681-5p tcGTAAAAaagaaga GUUUUACC m6b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4659a-3p tcgtaaAGAAGAAga UUUCUUCU m7b Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4659b-3p tcgtaaAGAAGAAga UUUCUUCU m7b Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4778-3p tcgtaAAGAAGAaga UCUUCUUC m7a Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-2681-5p tcGTAAAAaagaaga GUUUUACC m6b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4659a-3p tcgtaaAGAAGAAga UUUCUUCU m7b Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4659b-3p tcgtaaAGAAGAAga UUUCUUCU m7b Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4778-3p tcgtaAAGAAGAaga UCUUCUUC m7a Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837940C>A COSM1413508 TCGA-AA-3510-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-145-3p aAGGAATCtttcaat GGAUUCCU m7b Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-203a-3p aaggaatATTTCAat GUGAAAUG m6b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-145-3p aAGGAATCtttcaat GGAUUCCU m7b Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-203a-3p aaggaatATTTCAat GUGAAAUG m6b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837939T>C COSM1566112 TCGA-DC-6683-01 [large_intestine][rectum][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1252-5p aggaaTCCTTCaatg AGAAGGAA m6b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-541-5p aggAATCCTTcaatg AAAGGAUU m7b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-6126 aggaatCCTTCAatg GUGAAGGC m6b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-1252-5p aggaaTCCTTCaatg AGAAGGAA m6b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-541-5p aggAATCCTTcaatg AAAGGAUU m7b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-6126 aggaatCCTTCAatg GUGAAGGC m6b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837927C>G COSM3841676 TCGA-A2-A4S1-01 [breast][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1296-3p atgctatCCCCACTt GAGUGGGG m7b Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-3945 atgcTATGCCCactt AGGGCAUA m7b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4253 atgctATGCCCactt AGGGCAUG m6b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-491-5p atgctaTCCCCACTt AGUGGGGA m8a Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-6857-5p atgctATCCCCActt UUGGGGAU m7b Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-6862-5p atgctATGCCCactt CGGGCAUG m6b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-1296-3p atgctatCCCCACTt GAGUGGGG m7b Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-3945 atgcTATGCCCactt AGGGCAUA m7b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4253 atgctATGCCCactt AGGGCAUG m6b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-491-5p atgctaTCCCCACTt AGUGGGGA m8a Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-6857-5p atgctATCCCCActt UUGGGGAU m7b Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-6862-5p atgctATGCCCactt CGGGCAUG m6b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837910G>C COSM3963887 3093_T [lung][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1180-5p tcagcaTGGGTCatt GGACCCAC m6b Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-29c-5p tcagcATCGGTCAtt UGACCGAU m8a Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4728-3p TCAGCATGggtcatt CAUGCUGA m8a Disrupted HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-1180-5p tcagcaTGGGTCatt GGACCCAC m6b Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-29c-5p tcagcATCGGTCAtt UGACCGAU m8a Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4728-3p TCAGCATGggtcatt CAUGCUGA m8a Disrupted HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837906C>A COSM184285 TCGA-AA-3522-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4275 catggGTAATTGaag CCAAUUAC m7b Created HHHNA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696
hsa-miR-4275 catggGTAATTGaag CCAAUUAC m7b Created HHHSA_15093_ADAMTS1|NM_006988|exon_CDS|-6.97858086257819|-0.721580181167696

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837892G>T COSM318527 2334196 [lung][NS][carcinoma][small_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1180-5p gaGTGGGTCgaatgt GGACCCAC m7b (m6b->m7b) HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4286 gAGTGGGGcgaatgt ACCCCACU m7b Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4758-3p gaGTGGGGCgaatgt UGCCCCAC m7b (m7b->m6b) HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-551a gagTGGGTCGaatgt GCGACCCA m7b Created HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-551b-3p gagTGGGTCGaatgt GCGACCCA m7b Created HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-6726-3p gagtgGGGCGAatgt CUCGCCCU m6b Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-7114-3p gaGTGGGTCgaatgt UGACCCAC m7b (m6b->m7b) HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-1180-5p gaGTGGGTCgaatgt GGACCCAC m7b (m6b->m7b) HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4286 gAGTGGGGcgaatgt ACCCCACU m7b Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4758-3p gaGTGGGGCgaatgt UGCCCCAC m7b (m7b->m6b) HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-551a gagTGGGTCGaatgt GCGACCCA m7b Created HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-551b-3p gagTGGGTCGaatgt GCGACCCA m7b Created HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-6726-3p gagtgGGGCGAatgt CUCGCCCU m6b Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-7114-3p gaGTGGGTCgaatgt UGACCCAC m7b (m6b->m7b) HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837857A>C COSM1163290 PA285 [pancreas][NS][carcinoma][ductal_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-3191-5p ttggCAGAGAagact CUCUCUGG m6b Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-639 ttgGCAGCGAagact AUCGCUGC m7b Created HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-6728-3p ttgGCAGAGAagact UCUCUGCU m7a Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-6740-3p ttggcagAGAAGACt UGUCUUCU m7b Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-6809-3p ttggcAGAGAAGact CUUCUCUU m7a Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-942-5p ttggcAGAGAAGAct UCUUCUCU m8a Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-3191-5p ttggCAGAGAagact CUCUCUGG m6b Disrupted HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-639 ttgGCAGCGAagact AUCGCUGC m7b Created HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-6728-3p ttgGCAGAGAagact UCUCUGCU m7a Disrupted HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-6740-3p ttggcagAGAAGACt UGUCUUCU m7b Disrupted HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-6809-3p ttggcAGAGAAGact CUUCUCUU m7a Disrupted HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-942-5p ttggcAGAGAAGAct UCUUCUCU m8a Disrupted HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-3191-5p ttggCAGAGAagact CUCUCUGG m6b Disrupted HHHNH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-639 ttgGCAGCGAagact AUCGCUGC m7b Created HHHNH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-6728-3p ttgGCAGAGAagact UCUCUGCU m7a Disrupted HHHNH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-6740-3p ttggcagAGAAGACt UGUCUUCU m7b Disrupted HHHNH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-6809-3p ttggcAGAGAAGact CUUCUCUU m7a Disrupted HHHNH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-942-5p ttggcAGAGAAGAct UCUUCUCU m8a Disrupted HHHNH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-3191-5p ttggCAGAGAagact CUCUCUGG m6b Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-639 ttgGCAGCGAagact AUCGCUGC m7b Created HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-6728-3p ttgGCAGAGAagact UCUCUGCU m7a Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-6740-3p ttggcagAGAAGACt UGUCUUCU m7b Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-6809-3p ttggcAGAGAAGact CUUCUCUU m7a Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-942-5p ttggcAGAGAAGAct UCUUCUCU m8a Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-3191-5p ttggCAGAGAagact CUCUCUGG m6b Disrupted HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-639 ttgGCAGCGAagact AUCGCUGC m7b Created HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-6728-3p ttgGCAGAGAagact UCUCUGCU m7a Disrupted HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-6740-3p ttggcagAGAAGACt UGUCUUCU m7b Disrupted HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-6809-3p ttggcAGAGAAGact CUUCUCUU m7a Disrupted HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-942-5p ttggcAGAGAAGAct UCUUCUCU m8a Disrupted HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-3191-5p ttggCAGAGAagact CUCUCUGG m6b Disrupted HHHSH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-639 ttgGCAGCGAagact AUCGCUGC m7b Created HHHSH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-6728-3p ttgGCAGAGAagact UCUCUGCU m7a Disrupted HHHSH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-6740-3p ttggcagAGAAGACt UGUCUUCU m7b Disrupted HHHSH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-6809-3p ttggcAGAGAAGact CUUCUCUU m7a Disrupted HHHSH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642
hsa-miR-942-5p ttggcAGAGAAGAct UCUUCUCU m8a Disrupted HHHSH_57_ADAMTS1|NM_006988|exon_CDS|-8.93864640401146|0.353446114593642

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837846A>G COSM2841431 08-P1177 [bone][NS][Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4733-3p gaCTGGTGGaatgcc CCACCAGG m7a (m6a->m7a) HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-4733-3p gaCTGGTGGaatgcc CCACCAGG m7a (m6a->m7a) HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4733-3p gaCTGGTGGaatgcc CCACCAGG m7a (m6a->m7a) HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-4733-3p gaCTGGTGGaatgcc CCACCAGG m7a (m6a->m7a) HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837841G>T COSM1413507 TCGA-CM-6166-01 [large_intestine][colon][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1307-3p gtagaatGCCGAGac ACUCGGCG m6b Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-3917 gtagaatTCCGAGac GCUCGGAC m6b Created HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4304 gtagaATGCCGagac CCGGCAUG m6b Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4638-5p gtagaatGCCGAGac ACUCGGCU m6b Disrupted HHHNA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-1307-3p gtagaatGCCGAGac ACUCGGCG m6b Disrupted HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-3917 gtagaatTCCGAGac GCUCGGAC m6b Created HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-4304 gtagaATGCCGagac CCGGCAUG m6b Disrupted HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-4638-5p gtagaatGCCGAGac ACUCGGCU m6b Disrupted HHHNE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-1307-3p gtagaatGCCGAGac ACUCGGCG m6b Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-3917 gtagaatTCCGAGac GCUCGGAC m6b Created HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4304 gtagaATGCCGagac CCGGCAUG m6b Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-4638-5p gtagaatGCCGAGac ACUCGGCU m6b Disrupted HHHSA_15092_ADAMTS1|NM_006988|exon_CDS|-6.89886968519946|-1.1908417641979
hsa-miR-1307-3p gtagaatGCCGAGac ACUCGGCG m6b Disrupted HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-3917 gtagaatTCCGAGac GCUCGGAC m6b Created HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-4304 gtagaATGCCGagac CCGGCAUG m6b Disrupted HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945
hsa-miR-4638-5p gtagaatGCCGAGac ACUCGGCU m6b Disrupted HHHSE_320_ADAMTS1|NM_006988|exon_CDS|-7.41840105264201|-1.21955861416945

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837822G>T COSM1726457 186T [liver][NS][carcinoma][hepatocellular_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1265 atggACATCCTGctt CAGGAUGU m8a Created HHFCT_97525_uc002ymf.1_7_18
hsa-miR-219b-5p atGGACATCctgctt AGAUGUCC m7b (m6b->m7b) HHFCT_97525_uc002ymf.1_7_18
hsa-miR-3912-5p ATGGACATcctgctt AUGUCCAU m8a Created HHFCT_97525_uc002ymf.1_7_18
hsa-miR-4690-5p atggacaGCCTGCTt GAGCAGGC m7b Disrupted HHFCT_97525_uc002ymf.1_7_18
hsa-miR-6165 atggacaTCCTGCTt CAGCAGGA m7b Created HHFCT_97525_uc002ymf.1_7_18

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837814C>T COSM402229 LUAD-5V8LT [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6125 cctgCTTCCGagtgt GCGGAAGG m6b Disrupted HHFCT_97525_uc002ymf.1_7_18
hsa-miR-6828-5p ccTGCTTCCgagtgt AGGAAGCA m7b (m7b->m6b) HHFCT_97525_uc002ymf.1_7_18

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837757G>A COSM1029661 TCGA-D1-A0ZS-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1207-5p catCCCTGCCcccag UGGCAGGG m7b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-1237-5p catccctGCCCCCag CGGGGGCG m6b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-4488 catccctGCCCCCag AGGGGGCG m6b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-4697-5p catccctGCCCCCag AGGGGGCG m6b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-4763-3p catCCCTGCCcccag AGGCAGGG m7b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-486-3p catccCTGCCCCcag CGGGGCAG m7b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-6721-5p catcCCTGCCCccag UGGGCAGG m7b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-6751-5p catccctACCCCCAg UUGGGGGU m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-6752-5p catccctACCCCCag GGGGGGUG m6b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-6803-5p catccctACCCCCAg CUGGGGGU m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-6835-5p catcccTACCCCCag AGGGGGUA m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-1207-5p catCCCTGCCcccag UGGCAGGG m7b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-1237-5p catccctGCCCCCag CGGGGGCG m6b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4488 catccctGCCCCCag AGGGGGCG m6b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4697-5p catccctGCCCCCag AGGGGGCG m6b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4763-3p catCCCTGCCcccag AGGCAGGG m7b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-486-3p catccCTGCCCCcag CGGGGCAG m7b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6721-5p catcCCTGCCCccag UGGGCAGG m7b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6751-5p catccctACCCCCAg UUGGGGGU m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6752-5p catccctACCCCCag GGGGGGUG m6b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6803-5p catccctACCCCCAg CUGGGGGU m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6835-5p catcccTACCCCCag AGGGGGUA m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-1207-5p catCCCTGCCcccag UGGCAGGG m7b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-1237-5p catccctGCCCCCag CGGGGGCG m6b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4488 catccctGCCCCCag AGGGGGCG m6b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4697-5p catccctGCCCCCag AGGGGGCG m6b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4763-3p catCCCTGCCcccag AGGCAGGG m7b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-486-3p catccCTGCCCCcag CGGGGCAG m7b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6721-5p catcCCTGCCCccag UGGGCAGG m7b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6751-5p catccctACCCCCAg UUGGGGGU m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6752-5p catccctACCCCCag GGGGGGUG m6b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6803-5p catccctACCCCCAg CUGGGGGU m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6835-5p catcccTACCCCCag AGGGGGUA m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837754C>T COSM1179423 SWE-30 [prostate][NS][adenoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4763-3p CCCTGCCTccagtgg AGGCAGGG m8a Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-486-3p ccCTGCCCCcagtgg CGGGGCAG m7b (m7b->m6b) HHFKP_90797_uc002ymf.1_4_17
hsa-miR-637 ccctgCCCCCAGTgg ACUGGGGG m8a Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-650 cccTGCCTCCagtgg AGGAGGCA m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-6721-5p cCCTGCCCccagtgg UGGGCAGG m7b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-6808-5p cCCTGCCTccagtgg CAGGCAGG m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-6893-5p cCCTGCCTccagtgg CAGGCAGG m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-940 cCCTGCCTccagtgg AAGGCAGG m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-1237-5p ccctGCCCCCagtgg CGGGGGCG m6b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-1827 ccCTGCCTCcagtgg UGAGGCAG m7b (m6b->m7b) HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-3612 cccTGCCTCCagtgg AGGAGGCA m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4443 ccctGCCTCCAgtgg UUGGAGGC m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4488 ccctGCCCCCagtgg AGGGGGCG m6b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4697-5p ccctGCCCCCagtgg AGGGGGCG m6b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4763-3p CCCTGCCTccagtgg AGGCAGGG m8a Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-486-3p ccCTGCCCCcagtgg CGGGGCAG m7b (m7b->m6b) HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-637 ccctgCCCCCAGTgg ACUGGGGG m8a Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-650 cccTGCCTCCagtgg AGGAGGCA m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6721-5p cCCTGCCCccagtgg UGGGCAGG m7b Disrupted HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6808-5p cCCTGCCTccagtgg CAGGCAGG m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6893-5p cCCTGCCTccagtgg CAGGCAGG m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-940 cCCTGCCTccagtgg AAGGCAGG m7b Created HHHNA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-1237-5p ccctGCCCCCagtgg CGGGGGCG m6b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-1827 ccCTGCCTCcagtgg UGAGGCAG m7b (m6b->m7b) HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-3612 cccTGCCTCCagtgg AGGAGGCA m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4443 ccctGCCTCCAgtgg UUGGAGGC m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4488 ccctGCCCCCagtgg AGGGGGCG m6b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4697-5p ccctGCCCCCagtgg AGGGGGCG m6b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-4763-3p CCCTGCCTccagtgg AGGCAGGG m8a Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-486-3p ccCTGCCCCcagtgg CGGGGCAG m7b (m7b->m6b) HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-637 ccctgCCCCCAGTgg ACUGGGGG m8a Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-650 cccTGCCTCCagtgg AGGAGGCA m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6721-5p cCCTGCCCccagtgg UGGGCAGG m7b Disrupted HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6808-5p cCCTGCCTccagtgg CAGGCAGG m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-6893-5p cCCTGCCTccagtgg CAGGCAGG m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-940 cCCTGCCTccagtgg AAGGCAGG m7b Created HHHSA_15091_ADAMTS1|NM_006988|exon_CDS|-7.55820098449756|-0.747990226887369
hsa-miR-1237-5p ccctGCCCCCagtgg CGGGGGCG m6b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-1827 ccCTGCCTCcagtgg UGAGGCAG m7b (m6b->m7b) HHFKP_90797_uc002ymf.1_4_17
hsa-miR-3612 cccTGCCTCCagtgg AGGAGGCA m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-4443 ccctGCCTCCAgtgg UUGGAGGC m7b Created HHFKP_90797_uc002ymf.1_4_17
hsa-miR-4488 ccctGCCCCCagtgg AGGGGGCG m6b Disrupted HHFKP_90797_uc002ymf.1_4_17
hsa-miR-4697-5p ccctGCCCCCagtgg AGGGGGCG m6b Disrupted HHFKP_90797_uc002ymf.1_4_17

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837693A>C COSM4751745 pfg217T [stomach][NS][carcinoma][intestinal_adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-103a-2-5p acaaaaaAAGAAGCt AGCUUCUU m7b Disrupted HHHNE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-3182 acaaaaACAGAAGCt GCUUCUGU m8a Created HHHNE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-4652-3p acaaaAACAGAAgct GUUCUGUU m7b Created HHHNE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-103a-2-5p acaaaaaAAGAAGCt AGCUUCUU m7b Disrupted HHHSE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-3182 acaaaaACAGAAGCt GCUUCUGU m8a Created HHHSE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-4652-3p acaaaAACAGAAgct GUUCUGUU m7b Created HHHSE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837671C>T COSM578769 TCGA-64-1676-01 [lung][NS][carcinoma][adenocarcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1302 tcTGTCCCAtgatgg UUGGGACA m7b (m7b->m6b) HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-2681-3p tctgtcCCATGATgg UAUCAUGG m7b Disrupted HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-4298 tcTGTCCCAtgatgg CUGGGACA m7b (m7b->m6b) HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6871-5p tctgTCCCATGatgg CAUGGGAG m7a Disrupted HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-1302 tcTGTCCCAtgatgg UUGGGACA m7b (m7b->m6b) HHHNE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-2681-3p tctgtcCCATGATgg UAUCAUGG m7b Disrupted HHHNE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-4298 tcTGTCCCAtgatgg CUGGGACA m7b (m7b->m6b) HHHNE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-6871-5p tctgTCCCATGatgg CAUGGGAG m7a Disrupted HHHNE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-1302 tcTGTCCCAtgatgg UUGGGACA m7b (m7b->m6b) HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-2681-3p tctgtcCCATGATgg UAUCAUGG m7b Disrupted HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-4298 tcTGTCCCAtgatgg CUGGGACA m7b (m7b->m6b) HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6871-5p tctgTCCCATGatgg CAUGGGAG m7a Disrupted HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-1302 tcTGTCCCAtgatgg UUGGGACA m7b (m7b->m6b) HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-2681-3p tctgtcCCATGATgg UAUCAUGG m7b Disrupted HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-4298 tcTGTCCCAtgatgg CUGGGACA m7b (m7b->m6b) HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6871-5p tctgTCCCATGatgg CAUGGGAG m7a Disrupted HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-1302 tcTGTCCCAtgatgg UUGGGACA m7b (m7b->m6b) HHHSE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-2681-3p tctgtcCCATGATgg UAUCAUGG m7b Disrupted HHHSE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-4298 tcTGTCCCAtgatgg CUGGGACA m7b (m7b->m6b) HHHSE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-6871-5p tctgTCCCATGatgg CAUGGGAG m7a Disrupted HHHSE_319_ADAMTS1|NM_006988|exon_CDS|-8.29886040394044|-1.12772808854191
hsa-miR-1302 tcTGTCCCAtgatgg UUGGGACA m7b (m7b->m6b) HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-2681-3p tctgtcCCATGATgg UAUCAUGG m7b Disrupted HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-4298 tcTGTCCCAtgatgg CUGGGACA m7b (m7b->m6b) HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6871-5p tctgTCCCATGatgg CAUGGGAG m7a Disrupted HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-1302 tcTGTCCCAtgatgg UUGGGACA m7b (m7b->m6b) HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-2681-3p tctgtcCCATGATgg UAUCAUGG m7b Disrupted HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-4298 tcTGTCCCAtgatgg CUGGGACA m7b (m7b->m6b) HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-6871-5p tctgTCCCATGatgg CAUGGGAG m7a Disrupted HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837661G>A COSM1029659 TCGA-AX-A0J1-01 [endometrium][NS][carcinoma][endometrioid_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6800-3p gatgGAGAGGTGtta CACCUCUC m8a Created HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6887-3p gatGGAGGGGtgtta UCCCCUCC m7b Disrupted HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6800-3p gatgGAGAGGTGtta CACCUCUC m8a Created HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6887-3p gatGGAGGGGtgtta UCCCCUCC m7b Disrupted HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6800-3p gatgGAGAGGTGtta CACCUCUC m8a Created HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6887-3p gatGGAGGGGtgtta UCCCCUCC m7b Disrupted HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6800-3p gatgGAGAGGTGtta CACCUCUC m8a Created HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6887-3p gatGGAGGGGtgtta UCCCCUCC m7b Disrupted HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6800-3p gatgGAGAGGTGtta CACCUCUC m8a Created HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-6887-3p gatGGAGGGGtgtta UCCCCUCC m7b Disrupted HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837660G>A COSM4540324 CSCC-49-T [skin][head_neck][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-483-3p atggAGGAGTGttat UCACUCCU m7b Created HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6792-3p aTGGAGGAGtgttat CUCCUCCA m8a (m7a->m8a) HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6887-3p atGGAGGGGtgttat UCCCCUCC m7b (m7b->m6b) HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-21-3p atggaggGGTGTTat CAACACCA m6b Disrupted HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-3591-3p atggaggGGTGTTat AAACACCA m6b Disrupted HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-483-3p atggAGGAGTGttat UCACUCCU m7b Created HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6792-3p aTGGAGGAGtgttat CUCCUCCA m8a (m7a->m8a) HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6887-3p atGGAGGGGtgttat UCCCCUCC m7b (m7b->m6b) HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-21-3p atggaggGGTGTTat CAACACCA m6b Disrupted HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-3591-3p atggaggGGTGTTat AAACACCA m6b Disrupted HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-483-3p atggAGGAGTGttat UCACUCCU m7b Created HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6792-3p aTGGAGGAGtgttat CUCCUCCA m8a (m7a->m8a) HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6887-3p atGGAGGGGtgttat UCCCCUCC m7b (m7b->m6b) HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-21-3p atggaggGGTGTTat CAACACCA m6b Disrupted HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-3591-3p atggaggGGTGTTat AAACACCA m6b Disrupted HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-483-3p atggAGGAGTGttat UCACUCCU m7b Created HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-6792-3p aTGGAGGAGtgttat CUCCUCCA m8a (m7a->m8a) HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-6887-3p atGGAGGGGtgttat UCCCCUCC m7b (m7b->m6b) HHKTA_34535_NM_006988|3255|3294|2.16339705258786|2.2823351383058
hsa-miR-21-3p atggaggGGTGTTat CAACACCA m6b Disrupted HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-3591-3p atggaggGGTGTTat AAACACCA m6b Disrupted HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-483-3p atggAGGAGTGttat UCACUCCU m7b Created HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6792-3p aTGGAGGAGtgttat CUCCUCCA m8a (m7a->m8a) HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6887-3p atGGAGGGGtgttat UCCCCUCC m7b (m7b->m6b) HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-21-3p atggaggGGTGTTat CAACACCA m6b Disrupted HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-3591-3p atggaggGGTGTTat AAACACCA m6b Disrupted HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837641T>C COSM4973009 1N21-VS-1T21 [oesophagus][NS][carcinoma][squamous_cell_carcinoma]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-6741-3p tgAGAGCCGtgatcc UCGGCUCU m7b (m6b->m7b) HHHNA_15089_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6741-3p tgAGAGCCGtgatcc UCGGCUCU m7b (m6b->m7b) HHHNA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6741-3p tgAGAGCCGtgatcc UCGGCUCU m7b (m6b->m7b) HHHNH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6741-3p tgAGAGCCGtgatcc UCGGCUCU m7b (m6b->m7b) HHHSA_15089_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6741-3p tgAGAGCCGtgatcc UCGGCUCU m7b (m6b->m7b) HHHSA_15090_ADAMTS1|NM_006988|exon_CDS|-7.44796342140664|1.49310205655618
hsa-miR-6741-3p tgAGAGCCGtgatcc UCGGCUCU m7b (m6b->m7b) HHHSH_56_ADAMTS1|NM_006988|exon_CDS|-8.6749582253155|-0.993344394186994
hsa-miR-6741-3p tgAGAGCCGtgatcc UCGGCUCU m7b (m6b->m7b) HHKTA_46316_NM_006988|3295|3334|1.55764587786326|2.2823351383058

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26837485G>T COSN5768513 HCC167T [liver][NS][carcinoma][NS]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-1243 gtatcttTCCAGTaa AACUGGAU m6b Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-193a-3p gtatcttGCCAGTaa AACUGGCC m6b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-193b-3p gtatcttGCCAGTaa AACUGGCC m6b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3128 gtatcTTGCCAGtaa UCUGGCAA m7b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-31-5p gtaTCTTGCCagtaa AGGCAAGA m7b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3654 gtatcttTCCAGTaa GACUGGAC m6b Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3978 gtatCTTTCCAgtaa GUGGAAAG m7b Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-4799-3p gtatctTGCCAGTaa ACUGGCAU m7a Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-5588-5p gtatctTGCCAGTaa ACUGGCAU m7a Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-6128 gtatctTTCCAGTaa ACUGGAAU m7a Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-6868-5p gtatctTGCCAGTaa ACUGGCAG m7a Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-875-3p gtatcTTTCCAGtaa CCUGGAAA m7b Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-892b gtatcttGCCAGTaa CACUGGCU m6b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-1243 gtatcttTCCAGTaa AACUGGAU m6b Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-193a-3p gtatcttGCCAGTaa AACUGGCC m6b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-193b-3p gtatcttGCCAGTaa AACUGGCC m6b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3128 gtatcTTGCCAGtaa UCUGGCAA m7b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-31-5p gtaTCTTGCCagtaa AGGCAAGA m7b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3654 gtatcttTCCAGTaa GACUGGAC m6b Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3978 gtatCTTTCCAgtaa GUGGAAAG m7b Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-4799-3p gtatctTGCCAGTaa ACUGGCAU m7a Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-5588-5p gtatctTGCCAGTaa ACUGGCAU m7a Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-6128 gtatctTTCCAGTaa ACUGGAAU m7a Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-6868-5p gtatctTGCCAGTaa ACUGGCAG m7a Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-875-3p gtatcTTTCCAGtaa CCUGGAAA m7b Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-892b gtatcttGCCAGTaa CACUGGCU m6b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-1243 gtatcttTCCAGTaa AACUGGAU m6b Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-193a-3p gtatcttGCCAGTaa AACUGGCC m6b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-193b-3p gtatcttGCCAGTaa AACUGGCC m6b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3128 gtatcTTGCCAGtaa UCUGGCAA m7b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-31-5p gtaTCTTGCCagtaa AGGCAAGA m7b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3654 gtatcttTCCAGTaa GACUGGAC m6b Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3978 gtatCTTTCCAgtaa GUGGAAAG m7b Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-4799-3p gtatctTGCCAGTaa ACUGGCAU m7a Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-5588-5p gtatctTGCCAGTaa ACUGGCAU m7a Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-6128 gtatctTTCCAGTaa ACUGGAAU m7a Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-6868-5p gtatctTGCCAGTaa ACUGGCAG m7a Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-875-3p gtatcTTTCCAGtaa CCUGGAAA m7b Created HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-892b gtatcttGCCAGTaa CACUGGCU m6b Disrupted HHHNE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-1243 gtatcttTCCAGTaa AACUGGAU m6b Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-193a-3p gtatcttGCCAGTaa AACUGGCC m6b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-193b-3p gtatcttGCCAGTaa AACUGGCC m6b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3128 gtatcTTGCCAGtaa UCUGGCAA m7b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-31-5p gtaTCTTGCCagtaa AGGCAAGA m7b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3654 gtatcttTCCAGTaa GACUGGAC m6b Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-3978 gtatCTTTCCAgtaa GUGGAAAG m7b Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-4799-3p gtatctTGCCAGTaa ACUGGCAU m7a Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-5588-5p gtatctTGCCAGTaa ACUGGCAU m7a Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-6128 gtatctTTCCAGTaa ACUGGAAU m7a Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-6868-5p gtatctTGCCAGTaa ACUGGCAG m7a Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-875-3p gtatcTTTCCAGtaa CCUGGAAA m7b Created HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402
hsa-miR-892b gtatcttGCCAGTaa CACUGGCU m6b Disrupted HHHSE_317_ADAMTS1|NM_006988|exon_utr3|-7.05703524470311|-0.231714156722402

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26836895T>G COSN9155143 AOCS-149-1-7 [ovary][NS][other][neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HHFCT_97522_uc002ymf.1_4_18
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HHHNA_15084_ADAMTS1|NM_006988|exon_utr3|-5.59525051500271|3.05163036755362
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HHHNE_312_ADAMTS1|NM_006988|exon_utr3|-7.19176276392884|-0.0256323648819231
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HHHNH_53_ADAMTS1|NM_006988|exon_utr3|-8.68240600021063|-0.5485743264538
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HHHSA_15084_ADAMTS1|NM_006988|exon_utr3|-5.59525051500271|3.05163036755362
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HHHSE_312_ADAMTS1|NM_006988|exon_utr3|-7.19176276392884|-0.0256323648819231
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HHHSH_53_ADAMTS1|NM_006988|exon_utr3|-8.68240600021063|-0.5485743264538
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HHKTA_4014_NM_006988|4026|4065|15.5331908375808|2.2823351383058
hsa-miR-5585-3p tattTATTCAagtgc CUGAAUAG m6b Disrupted HPKTA_39548_G42537.1_28209213

Mutation Mutation ID Sample Name Cancer Type
chr21:g.26836405T>G COSN9155142 AOCS-137-3-7 [ovary][NS][other][neoplasm]
miRNA Targets Table
miR ID miRSite miRSeed SeedClass FuncClass Cluster ID
hsa-miR-4803 tatTTATGTTtatac UAACAUAA m7b Created HPHES_5103_G6783.1_28208730
hsa-miR-548c-3p tatttATTTTTatac CAAAAAUC m6b Disrupted HPHES_5103_G6783.1_28208730
hsa-miR-4803 tatTTATGTTtatac UAACAUAA m7b Created HPKTA_39544_G42533.2_28208743
hsa-miR-548c-3p tatttATTTTTatac CAAAAAUC m6b Disrupted HPKTA_39544_G42533.2_28208743
hsa-miR-4803 tatTTATGTTtatac UAACAUAA m7b Created HPRO6_50755_G60148.2_28208714
hsa-miR-548c-3p tatttATTTTTatac CAAAAAUC m6b Disrupted HPRO6_50755_G60148.2_28208714

*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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