PIAS1
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA156843430868434308+Missense_MutationSNPGGATCGA-DK-A6AW-01A-11D-A30E-08TCGA-DK-A6AW-10A-01D-A30H-08g.chr15:68434308G>Ac.494G>Ac.(493-495)cGa>cAap.R165Q
BLCA156846615168466151+Nonsense_MutationSNPCCTTCGA-DK-AA6L-01A-11D-A391-08TCGA-DK-AA6L-10A-01D-A394-08g.chr15:68466151C>Tc.1090C>Tc.(1090-1092)Cag>Tagp.Q364*
BLCA156846881968468819+Missense_MutationSNPGGCTCGA-FD-A6TC-01A-21D-A339-08TCGA-FD-A6TC-10A-21D-A339-08g.chr15:68468819G>Cc.1308G>Cc.(1306-1308)ttG>ttCp.L436F
BRCA156843893168438931+Missense_MutationSNPGGTTCGA-A2-A25A-01A-12D-A16D-09TCGA-A2-A25A-10A-01D-A16D-09g.chr15:68438931G>Tc.721G>Tc.(721-723)Gtg>Ttgp.V241L
BRCA156843894468438944+Missense_MutationSNPGGTTCGA-A2-A25A-01A-12D-A16D-09TCGA-A2-A25A-10A-01D-A16D-09g.chr15:68438944G>Tc.734G>Tc.(733-735)cGa>cTap.R245L
BRCA156846611868466118+Missense_MutationSNPCCTTCGA-C8-A26Y-01A-11D-A16D-09TCGA-C8-A26Y-10A-01D-A16D-09g.chr15:68466118C>Tc.1057C>Tc.(1057-1059)Cat>Tatp.H353Y
COAD156837869868378698+Missense_MutationSNPGGATCGA-AA-3947-01A-01W-0995-10TCGA-AA-3947-10A-01W-0995-10g.chr15:68378698G>Ac.79G>Ac.(79-81)Ggg>Aggp.G27R
COAD156837893368378933+Nonsense_MutationSNPCCATCGA-AA-3660-01A-01D-1719-10TCGA-AA-3660-11A-01D-1719-10g.chr15:68378933C>Ac.314C>Ac.(313-315)tCa>tAap.S105*
COAD156837902168379021+SilentSNPGGATCGA-AA-A01S-01A-21W-A096-10TCGA-AA-A01S-11A-21W-A096-10g.chr15:68379021G>Ac.402G>Ac.(400-402)ccG>ccAp.P134P
COAD156843429168434291+SilentSNPCCTTCGA-AU-6004-01A-11D-1719-10TCGA-AU-6004-10A-01D-1719-10g.chr15:68434291C>Tc.477C>Tc.(475-477)gaC>gaTp.D159D
COAD156843429168434291+SilentSNPCCTTCGA-D5-5540-01A-01D-1650-10TCGA-D5-5540-10A-01D-1650-10g.chr15:68434291C>Tc.477C>Tc.(475-477)gaC>gaTp.D159D
COAD156844593568445935+Missense_MutationSNPCCTTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr15:68445935C>Tc.836C>Tc.(835-837)tCc>tTcp.S279F
COAD156846610168466101+Missense_MutationSNPGGATCGA-AA-3715-01A-01W-0900-09TCGA-AA-3715-10A-01W-0900-09g.chr15:68466101G>Ac.1040G>Ac.(1039-1041)cGg>cAgp.R347Q
COAD156846892268468922+Nonsense_MutationSNPGGTTCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr15:68468922G>Tc.1411G>Tc.(1411-1413)Gag>Tagp.E471*
COADREAD156837869868378698+Missense_MutationSNPGGATCGA-AA-3947-01A-01W-0995-10TCGA-AA-3947-10A-01W-0995-10g.chr15:68378698G>Ac.79G>Ac.(79-81)Ggg>Aggp.G27R
COADREAD156837893368378933+Nonsense_MutationSNPCCATCGA-AA-3660-01A-01D-1719-10TCGA-AA-3660-11A-01D-1719-10g.chr15:68378933C>Ac.314C>Ac.(313-315)tCa>tAap.S105*
COADREAD156837902168379021+SilentSNPGGATCGA-AA-A01S-01A-21W-A096-10TCGA-AA-A01S-11A-21W-A096-10g.chr15:68379021G>Ac.402G>Ac.(400-402)ccG>ccAp.P134P
COADREAD156843429168434291+SilentSNPCCTTCGA-AU-6004-01A-11D-1719-10TCGA-AU-6004-10A-01D-1719-10g.chr15:68434291C>Tc.477C>Tc.(475-477)gaC>gaTp.D159D
COADREAD156843429168434291+SilentSNPCCTTCGA-D5-5540-01A-01D-1650-10TCGA-D5-5540-10A-01D-1650-10g.chr15:68434291C>Tc.477C>Tc.(475-477)gaC>gaTp.D159D
COADREAD156844593568445935+Missense_MutationSNPCCTTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr15:68445935C>Tc.836C>Tc.(835-837)tCc>tTcp.S279F
COADREAD156846610168466101+Missense_MutationSNPGGATCGA-AA-3715-01A-01W-0900-09TCGA-AA-3715-10A-01W-0900-09g.chr15:68466101G>Ac.1040G>Ac.(1039-1041)cGg>cAgp.R347Q
COADREAD156846892268468922+Nonsense_MutationSNPGGTTCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr15:68468922G>Tc.1411G>Tc.(1411-1413)Gag>Tagp.E471*
COADREAD156846898268468982+Missense_MutationSNPAACTCGA-AG-3892-01A-01W-1073-09TCGA-AG-3892-10A-01W-1073-09g.chr15:68468982A>Cc.1471A>Cc.(1471-1473)Aat>Catp.N491H
DLBC156847995968479959+Missense_MutationSNPTTCTCGA-GR-7353-01A-11D-2210-10TCGA-GR-7353-10A-01D-2210-10g.chr15:68479959T>Cc.1742T>Cc.(1741-1743)tTc>tCcp.F581S
ESCA156843429668434296+Missense_MutationSNPGGTTCGA-2H-A9GI-01A-11D-A37C-09TCGA-2H-A9GI-11A-11D-A37F-09g.chr15:68434296G>Tc.482G>Tc.(481-483)aGt>aTtp.S161I
ESCA156843893168438931+Missense_MutationSNPGGTTCGA-IG-A3YA-01A-11D-A247-09TCGA-IG-A3YA-10A-01D-A247-09g.chr15:68438931G>Tc.721G>Tc.(721-723)Gtg>Ttgp.V241L
ESCA156843893168438931+Missense_MutationSNPGGTTCGA-L5-A4OI-01A-11D-A27G-09TCGA-L5-A4OI-11A-11D-A27G-09g.chr15:68438931G>Tc.721G>Tc.(721-723)Gtg>Ttgp.V241L
ESCA156843894468438944+Missense_MutationSNPGGTTCGA-IG-A3YA-01A-11D-A247-09TCGA-IG-A3YA-10A-01D-A247-09g.chr15:68438944G>Tc.734G>Tc.(733-735)cGa>cTap.R245L
ESCA156843894468438944+Missense_MutationSNPGGTTCGA-IG-A4P3-01A-11D-A27G-09TCGA-IG-A4P3-10A-01D-A27G-09g.chr15:68438944G>Tc.734G>Tc.(733-735)cGa>cTap.R245L
ESCA156843894468438944+Missense_MutationSNPGGTTCGA-L5-A4OH-01A-11D-A27G-09TCGA-L5-A4OH-11A-11D-A27G-09g.chr15:68438944G>Tc.734G>Tc.(733-735)cGa>cTap.R245L
ESCA156843894468438944+Missense_MutationSNPGGTTCGA-L5-A4OI-01A-11D-A27G-09TCGA-L5-A4OI-11A-11D-A27G-09g.chr15:68438944G>Tc.734G>Tc.(733-735)cGa>cTap.R245L
GBM156846884168468841+Missense_MutationSNPGGTTCGA-06-0644-01A-02D-1492-08TCGA-06-0644-10A-01D-1492-08g.chr15:68468841G>Tc.1330G>Tc.(1330-1332)Gta>Ttap.V444L
GBMLGG156837874368378743+Missense_MutationSNPCCATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr15:68378743C>Ac.124C>Ac.(124-126)Ctg>Atgp.L42M
GBMLGG156846884168468841+Missense_MutationSNPGGTTCGA-06-0644-01A-02D-1492-08TCGA-06-0644-10A-01D-1492-08g.chr15:68468841G>Tc.1330G>Tc.(1330-1332)Gta>Ttap.V444L
GBMLGG156846889468468894+SilentSNPCCTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr15:68468894C>Tc.1383C>Tc.(1381-1383)gaC>gaTp.D461D
HNSC156847998468479984+Missense_MutationSNPTTGTCGA-BB-A5HY-01A-11D-A28R-08TCGA-BB-A5HY-10A-01D-A28U-08g.chr15:68479984T>Gc.1767T>Gc.(1765-1767)ttT>ttGp.F589L
KIPAN156843464468434644+Missense_MutationSNPAAGTCGA-A4-A5Y1-01A-11D-A28G-10TCGA-A4-A5Y1-11A-11D-A28G-10g.chr15:68434644A>Gc.571A>Gc.(571-573)Aaa>Gaap.K191E
KIPAN156843467568434675+Splice_SiteSNPGGATCGA-B0-5095-01A-01D-1421-08TCGA-B0-5095-11A-01D-1421-08g.chr15:68434675G>Ac.602G>Ac.(601-603)aGg>aAgp.R201K
KIPAN156844596668445966+SilentSNPCCTTCGA-AK-3451-01A-02D-1251-10TCGA-AK-3451-10A-01D-1251-10g.chr15:68445966C>Tc.867C>Tc.(865-867)tcC>tcTp.S289S
KIPAN156845709868457098+Missense_MutationSNPAAGTCGA-CZ-4859-01A-02D-1429-08TCGA-CZ-4859-11A-01D-1429-08g.chr15:68457098A>Gc.964A>Gc.(964-966)Agt>Ggtp.S322G
KIPAN156847999968479999+SilentSNPTTCTCGA-BQ-5876-01A-11D-1589-08TCGA-BQ-5876-11A-01D-1589-08g.chr15:68479999T>Cc.1782T>Cc.(1780-1782)agT>agCp.S594S
KIRC156843467568434675+Splice_SiteSNPGGATCGA-B0-5095-01A-01D-1421-08TCGA-B0-5095-11A-01D-1421-08g.chr15:68434675G>Ac.602G>Ac.(601-603)aGg>aAgp.R201K
KIRC156844596668445966+SilentSNPCCTTCGA-AK-3451-01A-02D-1251-10TCGA-AK-3451-10A-01D-1251-10g.chr15:68445966C>Tc.867C>Tc.(865-867)tcC>tcTp.S289S
KIRC156845709868457098+Missense_MutationSNPAAGTCGA-CZ-4859-01A-02D-1429-08TCGA-CZ-4859-11A-01D-1429-08g.chr15:68457098A>Gc.964A>Gc.(964-966)Agt>Ggtp.S322G
KIRP156843464468434644+Missense_MutationSNPAAGTCGA-A4-A5Y1-01A-11D-A28G-10TCGA-A4-A5Y1-11A-11D-A28G-10g.chr15:68434644A>Gc.571A>Gc.(571-573)Aaa>Gaap.K191E
KIRP156847999968479999+SilentSNPTTCTCGA-BQ-5876-01A-11D-1589-08TCGA-BQ-5876-11A-01D-1589-08g.chr15:68479999T>Cc.1782T>Cc.(1780-1782)agT>agCp.S594S
LGG156837874368378743+Missense_MutationSNPCCATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr15:68378743C>Ac.124C>Ac.(124-126)Ctg>Atgp.L42M
LGG156846889468468894+SilentSNPCCTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr15:68468894C>Tc.1383C>Tc.(1381-1383)gaC>gaTp.D461D
LUAD156837869568378695+Missense_MutationSNPGGTTCGA-44-3918-01A-01D-1105-08TCGA-44-3918-11A-01D-1105-08g.chr15:68378695G>Tc.76G>Tc.(76-78)Gcc>Tccp.A26S
LUAD156837869868378698+Frame_Shift_DelDELGG-TCGA-80-5611-01A-01D-1625-08TCGA-80-5611-10A-01D-1625-08g.chr15:68378698delGc.79delGc.(79-81)gggfsp.G27fs
LUSC156837891768378917+Missense_MutationSNPGGTTCGA-46-3768-01A-01D-0983-08TCGA-46-3768-10A-01D-0983-08g.chr15:68378917G>Tc.298G>Tc.(298-300)Gat>Tatp.D100Y
LUSC156843466968434669+Missense_MutationSNPAACTCGA-22-5492-01A-01D-1632-08TCGA-22-5492-11A-01D-1632-08g.chr15:68434669A>Cc.596A>Cc.(595-597)cAg>cCgp.Q199P
LUSC156846805868468058+Missense_MutationSNPCCTTCGA-56-6545-01A-11D-1817-08TCGA-56-6545-10A-01D-1817-08g.chr15:68468058C>Tc.1253C>Tc.(1252-1254)tCa>tTap.S418L
LUSC156846806868468068+Missense_MutationSNPAATTCGA-34-5231-01A-21D-1817-08TCGA-34-5231-10A-01D-1817-08g.chr15:68468068A>Tc.1263A>Tc.(1261-1263)gaA>gaTp.E421D
LUSC156847990468479904+Missense_MutationSNPGGTTCGA-63-5128-01A-01D-1441-08TCGA-63-5128-10A-01D-1441-08g.chr15:68479904G>Tc.1687G>Tc.(1687-1689)Gct>Tctp.A563S
OV156843429168434291+SilentSNPCCTTCGA-23-1022-01A-02W-0488-09TCGA-23-1022-10A-01W-0488-09g.chr15:68434291C>Tc.477C>Tc.(475-477)gaC>gaTp.D159D
PAAD156837908568379089+Splice_SiteDELCTAGGCTAGG-TCGA-3A-A9IV-01A-11D-A40W-08TCGA-3A-A9IV-10A-01D-A40W-08g.chr15:68379085_68379089delCTAGGc.466_469delCTAGGc.(466-471)ctaggc>gcp.LG156fs
PAAD156847993468479934+Missense_MutationSNPGGTTCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr15:68479934G>Tc.1717G>Tc.(1717-1719)Gac>Tacp.D573Y
PAAD156847997868479978+SilentSNPGGATCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr15:68479978G>Ac.1761G>Ac.(1759-1761)caG>caAp.Q587Q
READ156846898268468982+Missense_MutationSNPAACTCGA-AG-3892-01A-01W-1073-09TCGA-AG-3892-10A-01W-1073-09g.chr15:68468982A>Cc.1471A>Cc.(1471-1473)Aat>Catp.N491H
SARC156844600768446007+Missense_MutationSNPGGTTCGA-QQ-A5V2-01A-11D-A32I-09TCGA-QQ-A5V2-10A-01D-A32I-09g.chr15:68446007G>Tc.908G>Tc.(907-909)aGg>aTgp.R303M
SARC156846808968468089+Frame_Shift_DelDELTT-TCGA-WK-A8XX-01A-11D-A37C-09TCGA-WK-A8XX-10A-01D-A37F-09g.chr15:68468089delTc.1284delTc.(1282-1284)tctfsp.S428fs
SKCM156837901668379016+Missense_MutationSNPCCTTCGA-D3-A3MR-06A-11D-A21A-08TCGA-D3-A3MR-10A-01D-A21A-08g.chr15:68379016C>Tc.397C>Tc.(397-399)Cat>Tatp.H133Y
SKCM156843463868434638+Missense_MutationSNPGGATCGA-EE-A2A6-06A-11D-A197-08TCGA-EE-A2A6-10A-01D-A199-08g.chr15:68434638G>Ac.565G>Ac.(565-567)Ggg>Aggp.G189R
SKCM156844597968445979+Missense_MutationSNPCCTTCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr15:68445979C>Tc.880C>Tc.(880-882)Ctt>Tttp.L294F
SKCM156844601868446018+Missense_MutationSNPCCTTCGA-D3-A5GL-06A-11D-A27K-08TCGA-D3-A5GL-10A-01D-A27N-08g.chr15:68446018C>Tc.919C>Tc.(919-921)Cat>Tatp.H307Y
SKCM156845709268457092+Missense_MutationSNPCCTTCGA-EE-A3JB-06A-11D-A21A-08TCGA-EE-A3JB-10A-01D-A21A-08g.chr15:68457092C>Tc.958C>Tc.(958-960)Cca>Tcap.P320S
SKCM156845709368457093+Missense_MutationSNPCCTTCGA-EE-A3JB-06A-11D-A21A-08TCGA-EE-A3JB-10A-01D-A21A-08g.chr15:68457093C>Tc.959C>Tc.(958-960)cCa>cTap.P320L
SKCM156846899168468991+Splice_SiteSNPGGATCGA-EE-A3JA-06A-11D-A20D-08TCGA-EE-A3JA-10A-01D-A20D-08g.chr15:68468991G>Ac.1480G>Ac.(1480-1482)Ggc>Agcp.G494S
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BOCA-FR156846807268468072single base substitutionCTstop_gainedQ423*1267C>T
BOCA-FR156846807268468072single base substitutionCTstop_gainedQ425*1273C>T
BOCA-FR156846807268468072single base substitutionCTupstream_gene_variant
BRCA-EU156834251668342516single base substitutionGAupstream_gene_variant
BRCA-EU156834299068342990single base substitutionTAupstream_gene_variant
BRCA-EU156834327468343274single base substitutionGCupstream_gene_variant
BRCA-EU156834672268346722single base substitutionGCintron_variant
BRCA-EU156834672268346722single base substitutionGCupstream_gene_variant
BRCA-EU156834775168347751single base substitutionCTintron_variant
BRCA-EU156834943368349433single base substitutionCGintron_variant
BRCA-EU156835300668353006single base substitutionAGintron_variant
BRCA-EU156835438168354381single base substitutionGAintron_variant
BRCA-EU156835489368354893single base substitutionCTintron_variant
BRCA-EU156835931668359316single base substitutionTCintron_variant
BRCA-EU156835943768359437single base substitutionCGintron_variant
BRCA-EU156836050968360509single base substitutionGCintron_variant
BRCA-EU156836052468360524single base substitutionGAintron_variant
BRCA-EU156836337868363378single base substitutionGAintron_variant
BRCA-EU156836429768364297single base substitutionACintron_variant
BRCA-EU156836598668365986single base substitutionGAintron_variant
BRCA-EU156836657368366573single base substitutionGAintron_variant
BRCA-EU156836697768366977single base substitutionCAintron_variant
BRCA-EU156836705968367059single base substitutionGAintron_variant
BRCA-EU156836765868367658single base substitutionAGintron_variant
BRCA-EU156836845668368456single base substitutionTCintron_variant
BRCA-EU156837018068370180single base substitutionCTintron_variant
BRCA-EU156837218168372181deletion of <=200bpT-intron_variant
BRCA-EU156837400668374006single base substitutionGCintron_variant
BRCA-EU156837658468376584deletion of <=200bpT-intron_variant
BRCA-EU156837687068376870single base substitutionACintron_variant
BRCA-EU156838124168381241single base substitutionGAintron_variant
BRCA-EU156838230468382304single base substitutionGTintron_variant
BRCA-EU156838476268384762single base substitutionCGintron_variant
BRCA-EU156838557968385579single base substitutionCGintron_variant
BRCA-EU156838565568385655single base substitutionAGintron_variant
BRCA-EU156838647168386472deletion of <=200bpTA-intron_variant
BRCA-EU156838890668388906deletion of <=200bpT-intron_variant
BRCA-EU156839262568392625single base substitutionTGintron_variant
BRCA-EU156839456568394565single base substitutionCTintron_variant
BRCA-EU156839635868396358single base substitutionCGintron_variant
BRCA-EU156839652468396524single base substitutionGCintron_variant
BRCA-EU156839857868398578single base substitutionTAintron_variant
BRCA-EU156839881368398813single base substitutionGAintron_variant
BRCA-EU156839953268399532single base substitutionTCintron_variant
BRCA-EU156839999468399994single base substitutionTCintron_variant
BRCA-EU156840042068400420single base substitutionGAintron_variant
BRCA-EU156840265168402651single base substitutionGAintron_variant
BRCA-EU156840356968403569single base substitutionTCintron_variant
BRCA-EU156840485268404852deletion of <=200bpA-intron_variant
BRCA-EU156840828768408287single base substitutionGCintron_variant
BRCA-EU156840902668409026deletion of <=200bpT-intron_variant
BRCA-EU156840943968409467deletion of <=200bpCTTGAGACAAAGTCTCATTCTGTCTTGCC-intron_variant
BRCA-EU156841176268411762single base substitutionAGintron_variant
BRCA-EU156841252768412527single base substitutionCAintron_variant
BRCA-EU156841341768413417single base substitutionTCintron_variant
BRCA-EU156841447768414477single base substitutionCAintron_variant
BRCA-EU156841749468417494single base substitutionCGintron_variant
BRCA-EU156841839768418397single base substitutionTCintron_variant
BRCA-EU156841884968418849single base substitutionTAintron_variant
BRCA-EU156841962168419621deletion of <=200bpT-intron_variant
BRCA-EU156842118568421185single base substitutionGAintron_variant
BRCA-EU156842144968421449single base substitutionGCintron_variant
BRCA-EU156842178568421785single base substitutionGAintron_variant
BRCA-EU156842233268422332single base substitutionGTintron_variant
BRCA-EU156842253868422538single base substitutionATintron_variant
BRCA-EU156842335468423354single base substitutionTGintron_variant
BRCA-EU156842397668423976single base substitutionTGintron_variant
BRCA-EU156842711668427116single base substitutionCTintron_variant
BRCA-EU156843158868431588single base substitutionGTintron_variant
BRCA-EU156843257168432571single base substitutionCTintron_variant
BRCA-EU156843290368432903single base substitutionAGintron_variant
BRCA-EU156843355668433556single base substitutionGTintron_variant
BRCA-EU156843677168436771single base substitutionTAdownstream_gene_variant
BRCA-EU156843677168436771single base substitutionTAintron_variant
BRCA-EU156843677168436771single base substitutionTAupstream_gene_variant
BRCA-EU156843743968437439single base substitutionGCdownstream_gene_variant
BRCA-EU156843743968437439single base substitutionGCintron_variant
BRCA-EU156843743968437439single base substitutionGCupstream_gene_variant
BRCA-EU156843771868437718single base substitutionGTdownstream_gene_variant
BRCA-EU156843771868437718single base substitutionGTintron_variant
BRCA-EU156843771868437718single base substitutionGTupstream_gene_variant
BRCA-EU156843883168438831deletion of <=200bpT-downstream_gene_variant
BRCA-EU156843883168438831deletion of <=200bpT-intron_variant
BRCA-EU156843883168438831deletion of <=200bpT-upstream_gene_variant
BRCA-EU156844110268441109deletion of <=200bpTATTTCTT-intron_variant
BRCA-EU156844150968441509single base substitutionGCintron_variant
BRCA-EU156844261068442610single base substitutionAGintron_variant
BRCA-EU156844461468444614single base substitutionCTintron_variant
BRCA-EU156844508268445082single base substitutionTGintron_variant
BRCA-EU156844603868446038single base substitutionGAexon_variant
BRCA-EU156844603868446038single base substitutionGAsplice_region_variant
BRCA-EU156844702768447027single base substitutionAGdownstream_gene_variant
BRCA-EU156844702768447027single base substitutionAGintron_variant
BRCA-EU156844704368447043single base substitutionGAdownstream_gene_variant
BRCA-EU156844704368447043single base substitutionGAintron_variant
BRCA-EU156844704468447044single base substitutionCTdownstream_gene_variant
BRCA-EU156844704468447044single base substitutionCTintron_variant
BRCA-EU156844789268447892single base substitutionGCdownstream_gene_variant
BRCA-EU156844789268447892single base substitutionGCintron_variant
BRCA-EU156844837368448373single base substitutionTCdownstream_gene_variant
BRCA-EU156844837368448373single base substitutionTCintron_variant
BRCA-EU156844983068449830single base substitutionTCdownstream_gene_variant
BRCA-EU156844983068449830single base substitutionTCintron_variant
BRCA-EU156845232168452321single base substitutionAGintron_variant
BRCA-EU156845500068455000single base substitutionCGintron_variant
BRCA-EU156845532068455320single base substitutionGCintron_variant
BRCA-EU156845568868455688insertion of <=200bp-Tintron_variant
BRCA-EU156845779868457798single base substitutionCGintron_variant
BRCA-EU156845851068458510single base substitutionCTintron_variant
BRCA-EU156845982368459823single base substitutionCTintron_variant
BRCA-EU156846206468462064single base substitutionCGintron_variant
BRCA-EU156846298868462988deletion of <=200bpT-intron_variant
BRCA-EU156846298868462988insertion of <=200bp-Tintron_variant
BRCA-EU156846300368463003single base substitutionGCintron_variant
BRCA-EU156846332568463325single base substitutionGCintron_variant
BRCA-EU156846742768467427single base substitutionTCintron_variant
BRCA-EU156846742768467427single base substitutionTCupstream_gene_variant
BRCA-EU156846986068469860single base substitutionCTintron_variant
BRCA-EU156846986068469860single base substitutionCTupstream_gene_variant
BRCA-EU156847060868470608deletion of <=200bpA-intron_variant
BRCA-EU156847060868470608deletion of <=200bpA-upstream_gene_variant
BRCA-EU156847104768471047single base substitutionCTintron_variant
BRCA-EU156847104768471047single base substitutionCTupstream_gene_variant
BRCA-EU156847180868471808single base substitutionTCintron_variant
BRCA-EU156847180868471808single base substitutionTCupstream_gene_variant
BRCA-EU156847829168478291single base substitutionGTdownstream_gene_variant
BRCA-EU156847829168478291single base substitutionGTintron_variant
BRCA-EU156847903768479037deletion of <=200bpT-downstream_gene_variant
BRCA-EU156847903768479037deletion of <=200bpT-intron_variant
BRCA-EU156848029668480296deletion of <=200bpT-3_prime_UTR_variant
BRCA-EU156848050668480506single base substitutionGA3_prime_UTR_variant
BRCA-EU156848050668480506single base substitutionGAdownstream_gene_variant
BRCA-EU156848123468481234deletion of <=200bpA-downstream_gene_variant
BRCA-EU156848123468481234deletion of <=200bpA-intron_variant
BRCA-EU156848127368481273single base substitutionTCdownstream_gene_variant
BRCA-EU156848127368481273single base substitutionTCintron_variant
BRCA-EU156848145968481459deletion of <=200bpT-downstream_gene_variant
BRCA-EU156848145968481459deletion of <=200bpT-intron_variant
BRCA-EU156848201668482016single base substitutionGCdownstream_gene_variant
BRCA-EU156848201668482016single base substitutionGCintron_variant
BRCA-EU156848343568483436deletion of <=200bpTC-downstream_gene_variant
BRCA-EU156848343968483439insertion of <=200bp-Tdownstream_gene_variant
BRCA-EU156848376968483769single base substitutionCGdownstream_gene_variant
BRCA-EU156848426968484269single base substitutionCGdownstream_gene_variant
BRCA-EU156848697368486973single base substitutionCGdownstream_gene_variant
BRCA-FR156835132668351326single base substitutionCGintron_variant
BRCA-FR156835707268357072single base substitutionCTintron_variant
BRCA-FR156838305468383054single base substitutionGAintron_variant
BRCA-FR156838924868389248single base substitutionGTintron_variant
BRCA-FR156839262568392625single base substitutionTGintron_variant
BRCA-FR156839627668396276single base substitutionCGintron_variant
BRCA-FR156842517568425175single base substitutionCGintron_variant
BRCA-FR156843257168432571single base substitutionCTintron_variant
BRCA-FR156845851068458510single base substitutionCTintron_variant
BRCA-FR156845870068458700single base substitutionCTintron_variant
BRCA-FR156848376968483769single base substitutionCGdownstream_gene_variant
BRCA-FR156848807968488079single base substitutionGCdownstream_gene_variant
BRCA-UK156834739268347392single base substitutionCG5_prime_UTR_premature_start_codon_gain_variant
BRCA-UK156834739268347392single base substitutionCGintron_variant
BRCA-UK156838924668389246single base substitutionTGintron_variant
BRCA-UK156846742768467427single base substitutionTCintron_variant
BRCA-UK156846742768467427single base substitutionTCupstream_gene_variant
BRCA-UK156847362568473625single base substitutionTGexon_variant
BRCA-UK156847362568473625single base substitutionTGmissense_variantI519M1557T>G
BRCA-UK156847362568473625single base substitutionTGmissense_variantI521M1563T>G
BRCA-UK156847996068479960single base substitutionCA3_prime_UTR_variant
BRCA-UK156847996068479960single base substitutionCAmissense_variantF581L1743C>A
BRCA-UK156847996068479960single base substitutionCAmissense_variantF583L1749C>A
BRCA-UK156848127368481273single base substitutionTCdownstream_gene_variant
BRCA-UK156848127368481273single base substitutionTCintron_variant
BRCA-US156843893168438931single base substitutionGTdownstream_gene_variant
BRCA-US156843893168438931single base substitutionGTmissense_variantV241L721G>T
BRCA-US156843893168438931single base substitutionGTmissense_variantV243L727G>T
BRCA-US156843893168438931single base substitutionGTupstream_gene_variant
BRCA-US156843894468438944single base substitutionGTdownstream_gene_variant
BRCA-US156843894468438944single base substitutionGTmissense_variantR245L734G>T
BRCA-US156843894468438944single base substitutionGTmissense_variantR247L740G>T
BRCA-US156843894468438944single base substitutionGTupstream_gene_variant
BRCA-US156846611868466118single base substitutionCTmissense_variantH353Y1057C>T
BRCA-US156846611868466118single base substitutionCTmissense_variantH355Y1063C>T
BRCA-US156846611868466118single base substitutionCTupstream_gene_variant
BTCA-JP156838019968380199single base substitutionCT3_prime_UTR_variant
BTCA-JP156838019968380199single base substitutionCTintron_variant
BTCA-JP156843430868434308single base substitutionGC3_prime_UTR_variant
BTCA-JP156843430868434308single base substitutionGCmissense_variantR165P494G>C
BTCA-JP156843430868434308single base substitutionGCmissense_variantR167P500G>C
BTCA-JP156843430868434308single base substitutionGCupstream_gene_variant
BTCA-JP156844604068446040single base substitutionAGexon_variant
BTCA-JP156844604068446040single base substitutionAGsplice_region_variant
BTCA-JP156847593168475931deletion of <=200bpT-downstream_gene_variant
BTCA-JP156847593168475931deletion of <=200bpT-intron_variant
BTCA-JP156848628368486283single base substitutionGTdownstream_gene_variant
CLLE-ES156834954268349542single base substitutionTCintron_variant
CLLE-ES156835444368354443single base substitutionTGintron_variant
CLLE-ES156837057568370575single base substitutionCAintron_variant
CLLE-ES156838179368381793single base substitutionTCintron_variant
CLLE-ES156839811168398111single base substitutionCAintron_variant
CLLE-ES156841280268412802single base substitutionCTintron_variant
CLLE-ES156841425768414264deletion of <=200bpAGTGTTTG-intron_variant
CLLE-ES156844558868445588single base substitutionGAintron_variant
CLLE-ES156845353068453530single base substitutionTCintron_variant
CLLE-ES156845722568457225single base substitutionTCintron_variant
CLLE-ES156846427268464272single base substitutionATintron_variant
CLLE-ES156846427268464272single base substitutionATupstream_gene_variant
CLLE-ES156847386468473864single base substitutionTCexon_variant
CLLE-ES156847386468473864single base substitutionTCintron_variant
COAD-US156837893368378933single base substitutionCA3_prime_UTR_variant
COAD-US156837893368378933single base substitutionCAexon_variant
COAD-US156837893368378933single base substitutionCAstop_gainedS105*314C>A
COAD-US156837893368378933single base substitutionCAstop_gainedS107*320C>A
COAD-US156843892168438921deletion of <=200bpA-downstream_gene_variant
COAD-US156843892168438921deletion of <=200bpA-frameshift_variantT237
COAD-US156843892168438921deletion of <=200bpA-frameshift_variantT239
COAD-US156843892168438921deletion of <=200bpA-upstream_gene_variant
COAD-US156844593568445935single base substitutionCTexon_variant
COAD-US156844593568445935single base substitutionCTmissense_variantS279F836C>T
COAD-US156844593568445935single base substitutionCTmissense_variantS281F842C>T
COCA-CN156834663668346636single base substitutionTC5_prime_UTR_variant
COCA-CN156834663668346636single base substitutionTCupstream_gene_variant
COCA-CN156834808668348086single base substitutionACintron_variant
COCA-CN156834810768348107single base substitutionTCintron_variant
COCA-CN156835457068354570single base substitutionCTintron_variant
COCA-CN156843422468434224single base substitutionGTintron_variant
COCA-CN156843422468434224single base substitutionGTupstream_gene_variant
COCA-CN156843434568434345single base substitutionAG3_prime_UTR_variant
COCA-CN156843434568434345single base substitutionAGsynonymous_variantQ177Q531A>G
COCA-CN156843434568434345single base substitutionAGsynonymous_variantQ179Q537A>G
COCA-CN156843434568434345single base substitutionAGupstream_gene_variant
COCA-CN156843440768434407single base substitutionGTintron_variant
COCA-CN156843440768434407single base substitutionGTupstream_gene_variant
COCA-CN156843810368438103single base substitutionAGdownstream_gene_variant
COCA-CN156843810368438103single base substitutionAGintron_variant
COCA-CN156843810368438103single base substitutionAGupstream_gene_variant
COCA-CN156843888168438881single base substitutionACdownstream_gene_variant
COCA-CN156843888168438881single base substitutionACintron_variant
COCA-CN156843888168438881single base substitutionACupstream_gene_variant
COCA-CN156844603768446037single base substitutionCTexon_variant
COCA-CN156844603768446037single base substitutionCTsplice_region_variant
COCA-CN156846622368466223single base substitutionAGmissense_variantI388V1162A>G
COCA-CN156846622368466223single base substitutionAGmissense_variantI390V1168A>G
COCA-CN156846622368466223single base substitutionAGupstream_gene_variant
COCA-CN156847986068479860single base substitutionCAintron_variant
EOPC-DE156838833768388337single base substitutionCTintron_variant
EOPC-DE156847408968474089single base substitutionCGexon_variant
EOPC-DE156847408968474089single base substitutionCGintron_variant
EOPC-DE156847787968477879single base substitutionGAdownstream_gene_variant
EOPC-DE156847787968477879single base substitutionGAintron_variant
ESAD-UK156834270768342707single base substitutionGAupstream_gene_variant
ESAD-UK156834621468346214single base substitutionCAupstream_gene_variant
ESAD-UK156834629168346291single base substitutionTCupstream_gene_variant
ESAD-UK156835055468350554single base substitutionCTintron_variant
ESAD-UK156835269368352693single base substitutionGTintron_variant
ESAD-UK156835270168352701single base substitutionCTintron_variant
ESAD-UK156835334568353345single base substitutionAGintron_variant
ESAD-UK156835341068353410single base substitutionATintron_variant
ESAD-UK156835407468354074single base substitutionAGintron_variant
ESAD-UK156835871268358712single base substitutionGAintron_variant
ESAD-UK156836156568361565single base substitutionCGintron_variant
ESAD-UK156836160468361604single base substitutionCTintron_variant
ESAD-UK156836293868362938single base substitutionGAintron_variant
ESAD-UK156836436868364368single base substitutionGCintron_variant
ESAD-UK156836538268365382single base substitutionCTintron_variant
ESAD-UK156836699568366995insertion of <=200bp-Tintron_variant
ESAD-UK156836866168368661single base substitutionCTintron_variant
ESAD-UK156837031968370319single base substitutionTCintron_variant
ESAD-UK156837170768371707single base substitutionTAintron_variant
ESAD-UK156837663568376635deletion of <=200bpT-intron_variant
ESAD-UK156837691568376915single base substitutionAGintron_variant
ESAD-UK156838125468381254single base substitutionTGintron_variant
ESAD-UK156838314268383142single base substitutionATintron_variant
ESAD-UK156838543168385431single base substitutionTAintron_variant
ESAD-UK156838824168388241single base substitutionATintron_variant
ESAD-UK156838881868388818insertion of <=200bp-Gintron_variant
ESAD-UK156838905668389056single base substitutionTCintron_variant
ESAD-UK156838924868389248single base substitutionGTintron_variant
ESAD-UK156838977768389777single base substitutionTAintron_variant
ESAD-UK156839144568391445single base substitutionTCintron_variant
ESAD-UK156839201468392014single base substitutionGTintron_variant
ESAD-UK156839244868392448single base substitutionACintron_variant
ESAD-UK156839351868393518single base substitutionGAintron_variant
ESAD-UK156839592868395928single base substitutionCTintron_variant
ESAD-UK156839732468397324single base substitutionTCintron_variant
ESAD-UK156839814468398144deletion of <=200bpA-intron_variant
ESAD-UK156839815168398151single base substitutionATintron_variant
ESAD-UK156839945368399453single base substitutionGCintron_variant
ESAD-UK156840297068402970single base substitutionCTintron_variant
ESAD-UK156840386468403864single base substitutionAGintron_variant
ESAD-UK156840421868404218single base substitutionGAintron_variant
ESAD-UK156840421968404219single base substitutionCTintron_variant
ESAD-UK156840512668405126single base substitutionAGintron_variant
ESAD-UK156840602168406021single base substitutionAGintron_variant
ESAD-UK156840720668407206single base substitutionTGintron_variant
ESAD-UK156840814768408147deletion of <=200bpT-intron_variant
ESAD-UK156840939768409397single base substitutionTGintron_variant
ESAD-UK156841049068410490single base substitutionAGintron_variant
ESAD-UK156841384068413840single base substitutionGAintron_variant
ESAD-UK156842013568420135single base substitutionCGintron_variant
ESAD-UK156842183568421835single base substitutionATintron_variant
ESAD-UK156842328268423282single base substitutionTCintron_variant
ESAD-UK156842449268424492single base substitutionTAintron_variant
ESAD-UK156842571968425719single base substitutionCAintron_variant
ESAD-UK156843093068430930single base substitutionATintron_variant
ESAD-UK156843336068433360single base substitutionTAintron_variant
ESAD-UK156843336168433361single base substitutionATintron_variant
ESAD-UK156843421368434213single base substitutionTGintron_variant
ESAD-UK156843421368434213single base substitutionTGupstream_gene_variant
ESAD-UK156843963168439631single base substitutionCTdownstream_gene_variant
ESAD-UK156843963168439631single base substitutionCTintron_variant
ESAD-UK156844093568440935single base substitutionTGintron_variant
ESAD-UK156844101568441015single base substitutionGAintron_variant
ESAD-UK156844236868442368single base substitutionAGintron_variant
ESAD-UK156844297168442971single base substitutionTGintron_variant
ESAD-UK156844444968444449single base substitutionGAintron_variant
ESAD-UK156844591468445914single base substitutionCTintron_variant
ESAD-UK156844675568446755single base substitutionAGdownstream_gene_variant
ESAD-UK156844675568446755single base substitutionAGintron_variant
ESAD-UK156844844368448443single base substitutionAGdownstream_gene_variant
ESAD-UK156844844368448443single base substitutionAGintron_variant
ESAD-UK156845026768450270deletion of <=200bpTCTG-downstream_gene_variant
ESAD-UK156845026768450270deletion of <=200bpTCTG-intron_variant
ESAD-UK156845426768454267deletion of <=200bpA-intron_variant
ESAD-UK156845652468456524single base substitutionATintron_variant
ESAD-UK156845655468456554insertion of <=200bp-Aintron_variant
ESAD-UK156845771668457716single base substitutionCTintron_variant
ESAD-UK156845803268458032deletion of <=200bpA-intron_variant
ESAD-UK156846046568460470deletion of <=200bpACCTCC-intron_variant
ESAD-UK156846101868461018single base substitutionTAintron_variant
ESAD-UK156846422568464225single base substitutionTCintron_variant
ESAD-UK156846422568464225single base substitutionTCupstream_gene_variant
ESAD-UK156846657268466572single base substitutionGAintron_variant
ESAD-UK156846657268466572single base substitutionGAupstream_gene_variant
ESAD-UK156846714168467141single base substitutionGTintron_variant
ESAD-UK156846714168467141single base substitutionGTupstream_gene_variant
ESAD-UK156847047168470471single base substitutionGAintron_variant
ESAD-UK156847047168470471single base substitutionGAupstream_gene_variant
ESAD-UK156847113668471136single base substitutionTCintron_variant
ESAD-UK156847113668471136single base substitutionTCupstream_gene_variant
ESAD-UK156847118068471180single base substitutionCTintron_variant
ESAD-UK156847118068471180single base substitutionCTupstream_gene_variant
ESAD-UK156847373368473733single base substitutionAGintron_variant
ESAD-UK156847445668474456single base substitutionATdownstream_gene_variant
ESAD-UK156847445668474456single base substitutionATintron_variant
ESAD-UK156847613568476135single base substitutionCTdownstream_gene_variant
ESAD-UK156847613568476135single base substitutionCTintron_variant
ESAD-UK156847645968476459single base substitutionCTdownstream_gene_variant
ESAD-UK156847645968476459single base substitutionCTintron_variant
ESAD-UK156847774268477742single base substitutionTAdownstream_gene_variant
ESAD-UK156847774268477742single base substitutionTAintron_variant
ESAD-UK156848008168480081single base substitutionAC3_prime_UTR_variant
ESAD-UK156848008168480081single base substitutionACsynonymous_variantR622R1864A>C
ESAD-UK156848008168480081single base substitutionACsynonymous_variantR624R1870A>C
ESAD-UK156848296468482964single base substitutionCT3_prime_UTR_variant
ESAD-UK156848296468482964single base substitutionCTdownstream_gene_variant
ESAD-UK156848498168484981single base substitutionCTdownstream_gene_variant
ESAD-UK156848601168486011single base substitutionGTdownstream_gene_variant
ESAD-UK156848728268487282single base substitutionAGdownstream_gene_variant
ESCA-CN156843430168434301single base substitutionCT3_prime_UTR_variant
ESCA-CN156843430168434301single base substitutionCTmissense_variantR163C487C>T
ESCA-CN156843430168434301single base substitutionCTmissense_variantR165C493C>T
ESCA-CN156843430168434301single base substitutionCTupstream_gene_variant
ESCA-CN156848010168480101single base substitutionCG3_prime_UTR_variant
ESCA-CN156848010168480101single base substitutionCGsynonymous_variantT628T1884C>G
ESCA-CN156848010168480101single base substitutionCGsynonymous_variantT630T1890C>G
GBM-US156846884168468841single base substitutionGTmissense_variantV444L1330G>T
GBM-US156846884168468841single base substitutionGTmissense_variantV446L1336G>T
GBM-US156846884168468841single base substitutionGTupstream_gene_variant
KIRC-US156843467568434675single base substitutionGA3_prime_UTR_variant
KIRC-US156843467568434675single base substitutionGAmissense_variantR201K602G>A
KIRC-US156843467568434675single base substitutionGAmissense_variantR203K608G>A
KIRC-US156843467568434675single base substitutionGAupstream_gene_variant
KIRC-US156844596668445966single base substitutionCTexon_variant
KIRC-US156844596668445966single base substitutionCTsynonymous_variantS289S867C>T
KIRC-US156844596668445966single base substitutionCTsynonymous_variantS291S873C>T
KIRC-US156845709868457098single base substitutionAGmissense_variantS322G964A>G
KIRC-US156845709868457098single base substitutionAGmissense_variantS324G970A>G
KIRP-US156843464468434644single base substitutionAG3_prime_UTR_variant
KIRP-US156843464468434644single base substitutionAGmissense_variantK191E571A>G
KIRP-US156843464468434644single base substitutionAGmissense_variantK193E577A>G
KIRP-US156843464468434644single base substitutionAGupstream_gene_variant
KIRP-US156847999968479999single base substitutionTC3_prime_UTR_variant
KIRP-US156847999968479999single base substitutionTCsynonymous_variantS594S1782T>C
KIRP-US156847999968479999single base substitutionTCsynonymous_variantS596S1788T>C
LAML-KR156843422468434224single base substitutionGTintron_variant
LAML-KR156843422468434224single base substitutionGTupstream_gene_variant
LAML-KR156844591468445914single base substitutionCAintron_variant
LICA-CN156837883268378832single base substitutionGT3_prime_UTR_variant
LICA-CN156837883268378832single base substitutionGTexon_variant
LICA-CN156837883268378832single base substitutionGTsynonymous_variantT71T213G>T
LICA-CN156837883268378832single base substitutionGTsynonymous_variantT73T219G>T
LICA-CN156846608468466084single base substitutionGTsynonymous_variantR341R1023G>T
LICA-CN156846608468466084single base substitutionGTsynonymous_variantR343R1029G>T
LICA-CN156846608468466084single base substitutionGTupstream_gene_variant
LICA-FR156835792768357927insertion of <=200bp-Aintron_variant
LICA-FR156836741668367416single base substitutionCTintron_variant
LICA-FR156836959968369599single base substitutionTCintron_variant
LICA-FR156838074768380747single base substitutionAGintron_variant
LICA-FR156838157568381575single base substitutionAGintron_variant
LICA-FR156838403468384034single base substitutionAGintron_variant
LICA-FR156838786668387866deletion of <=200bpT-intron_variant
LICA-FR156839159868391598deletion of <=200bpT-intron_variant
LICA-FR156839930868399313deletion of <=200bpTAGCAT-intron_variant
LICA-FR156842576068425760single base substitutionCTintron_variant
LICA-FR156844723168447231single base substitutionATdownstream_gene_variant
LICA-FR156844723168447231single base substitutionATintron_variant
LICA-FR156845641668456416single base substitutionATintron_variant
LICA-FR156845858568458585single base substitutionAGintron_variant
LICA-FR156847476368474763insertion of <=200bp-AGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCGGAGTTTTGCTCTTATTGCTCAGGCTGCGTGdownstream_gene_variant
LICA-FR156847476368474763insertion of <=200bp-AGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCGGAGTTTTGCTCTTATTGCTCAGGCTGCGTGintron_variant
LICA-FR156848068068480680single base substitutionAGdownstream_gene_variant
LICA-FR156848068068480680single base substitutionAGintron_variant
LINC-JP156834301668343016single base substitutionATupstream_gene_variant
LINC-JP156834314168343141single base substitutionGTupstream_gene_variant
LINC-JP156835684468356844single base substitutionACintron_variant
LINC-JP156836362568363625deletion of <=200bpG-intron_variant
LINC-JP156836546068365460single base substitutionTGintron_variant
LINC-JP156838044368380443single base substitutionGTintron_variant
LINC-JP156838598268385982single base substitutionAGintron_variant
LINC-JP156838910368389103single base substitutionATintron_variant
LINC-JP156840139468401394single base substitutionAGintron_variant
LINC-JP156841963268419632single base substitutionGTintron_variant
LINC-JP156841963368419633single base substitutionCTintron_variant
LINC-JP156843421268434213deletion of <=200bpTT-intron_variant
LINC-JP156843421268434213deletion of <=200bpTT-upstream_gene_variant
LINC-JP156843751368437513single base substitutionTAdownstream_gene_variant
LINC-JP156843751368437513single base substitutionTAintron_variant
LINC-JP156843751368437513single base substitutionTAupstream_gene_variant
LINC-JP156845691568456915single base substitutionAGintron_variant
LINC-JP156845933068459330single base substitutionATintron_variant
LINC-JP156846625268466252single base substitutionTGintron_variant
LINC-JP156846625268466252single base substitutionTGupstream_gene_variant
LINC-JP156846821768468217single base substitutionAGintron_variant
LINC-JP156846821768468217single base substitutionAGupstream_gene_variant
LINC-JP156846932268469322single base substitutionACintron_variant
LINC-JP156846932268469322single base substitutionACupstream_gene_variant
LINC-JP156846963668469636single base substitutionGAintron_variant
LINC-JP156846963668469636single base substitutionGAupstream_gene_variant
LINC-JP156847482868474828single base substitutionCTdownstream_gene_variant
LINC-JP156847482868474828single base substitutionCTintron_variant
LINC-JP156847832268478322single base substitutionACdownstream_gene_variant
LINC-JP156847832268478322single base substitutionACintron_variant
LINC-JP156847980768479807single base substitutionTAintron_variant
LINC-JP156848629468486294insertion of <=200bp-Adownstream_gene_variant
LINC-JP156848646168486461single base substitutionTGdownstream_gene_variant
LINC-JP156848651468486514single base substitutionTCdownstream_gene_variant
LIRI-JP156834315368343153single base substitutionCTupstream_gene_variant
LIRI-JP156834529168345291single base substitutionTCupstream_gene_variant
LIRI-JP156834823568348235single base substitutionAGintron_variant
LIRI-JP156834823568348235single base substitutionAGmissense_variantQ5R14A>G
LIRI-JP156834865568348655single base substitutionCGintron_variant
LIRI-JP156834896668348966single base substitutionATintron_variant
LIRI-JP156834921968349219single base substitutionATintron_variant
LIRI-JP156835048968350489single base substitutionGTintron_variant
LIRI-JP156835191368351913single base substitutionGTintron_variant
LIRI-JP156835427968354279single base substitutionCAintron_variant
LIRI-JP156835616768356167single base substitutionTGintron_variant
LIRI-JP156835632168356321single base substitutionAGintron_variant
LIRI-JP156835643668356436single base substitutionGAintron_variant
LIRI-JP156835701868357018single base substitutionCGintron_variant
LIRI-JP156836177768361777single base substitutionATintron_variant
LIRI-JP156836223068362230single base substitutionGAintron_variant
LIRI-JP156836435868364358single base substitutionACintron_variant
LIRI-JP156836467868364678single base substitutionCTintron_variant
LIRI-JP156836469068364690single base substitutionACintron_variant
LIRI-JP156836489068364890single base substitutionGAintron_variant
LIRI-JP156836490168364901single base substitutionTAintron_variant
LIRI-JP156836493168364931single base substitutionAGintron_variant
LIRI-JP156836719668367197deletion of <=200bpGC-intron_variant
LIRI-JP156836819368368193single base substitutionCTintron_variant
LIRI-JP156836915968369159single base substitutionAGintron_variant
LIRI-JP156837107068371070single base substitutionAGintron_variant
LIRI-JP156837270568372705single base substitutionACintron_variant
LIRI-JP156837461068374610single base substitutionAGintron_variant
LIRI-JP156837628568376285single base substitutionAGintron_variant
LIRI-JP156837747368377473single base substitutionAGintron_variant
LIRI-JP156837758368377583single base substitutionGAintron_variant
LIRI-JP156837833768378337deletion of <=200bpA-intron_variant
LIRI-JP156837871668378716single base substitutionCT3_prime_UTR_variant
LIRI-JP156837871668378716single base substitutionCTexon_variant
LIRI-JP156837871668378716single base substitutionCTmissense_variantR33C97C>T
LIRI-JP156837871668378716single base substitutionCTmissense_variantR35C103C>T
LIRI-JP156838137968381379deletion of <=200bpC-intron_variant
LIRI-JP156838266768382667single base substitutionAGintron_variant
LIRI-JP156838311668383116single base substitutionAGintron_variant
LIRI-JP156838582168385821single base substitutionTGintron_variant
LIRI-JP156838710068387100single base substitutionATintron_variant
LIRI-JP156838876368388763single base substitutionAGintron_variant
LIRI-JP156839785568397855single base substitutionAGintron_variant
LIRI-JP156839851968398519single base substitutionGAintron_variant
LIRI-JP156840014868400148single base substitutionCAintron_variant
LIRI-JP156840084968400849single base substitutionAGintron_variant
LIRI-JP156840355168403551single base substitutionAGintron_variant
LIRI-JP156840513168405131single base substitutionTCintron_variant
LIRI-JP156840566768405667single base substitutionAGintron_variant
LIRI-JP156840830568408305single base substitutionGTintron_variant
LIRI-JP156840996768409967single base substitutionATintron_variant
LIRI-JP156841065168410651single base substitutionTCintron_variant
LIRI-JP156841264168412641single base substitutionAGintron_variant
LIRI-JP156841832468418324single base substitutionAGintron_variant
LIRI-JP156841952068419520single base substitutionCTintron_variant
LIRI-JP156841964068419640single base substitutionAGintron_variant
LIRI-JP156842175068421750single base substitutionTAintron_variant
LIRI-JP156842179468421794single base substitutionAGintron_variant
LIRI-JP156842543668425436single base substitutionAGintron_variant
LIRI-JP156842990668429906single base substitutionAGintron_variant
LIRI-JP156843069468430694single base substitutionCTintron_variant
LIRI-JP156843208568432085single base substitutionCTintron_variant
LIRI-JP156843366868433668single base substitutionCAintron_variant
LIRI-JP156843437968434379single base substitutionGAintron_variant
LIRI-JP156843437968434379single base substitutionGAupstream_gene_variant
LIRI-JP156843523668435236single base substitutionTCdownstream_gene_variant
LIRI-JP156843523668435236single base substitutionTCintron_variant
LIRI-JP156843523668435236single base substitutionTCupstream_gene_variant
LIRI-JP156843537668435376single base substitutionAGdownstream_gene_variant
LIRI-JP156843537668435376single base substitutionAGintron_variant
LIRI-JP156843537668435376single base substitutionAGupstream_gene_variant
LIRI-JP156843612568436125single base substitutionGTdownstream_gene_variant
LIRI-JP156843612568436125single base substitutionGTintron_variant
LIRI-JP156843612568436125single base substitutionGTupstream_gene_variant
LIRI-JP156843852268438522single base substitutionAGdownstream_gene_variant
LIRI-JP156843852268438522single base substitutionAGintron_variant
LIRI-JP156843852268438522single base substitutionAGupstream_gene_variant
LIRI-JP156844206668442066single base substitutionTCintron_variant
LIRI-JP156844260168442601single base substitutionACintron_variant
LIRI-JP156844306268443062single base substitutionCGintron_variant
LIRI-JP156844338968443389single base substitutionAGintron_variant
LIRI-JP156844658168446581deletion of <=200bpG-downstream_gene_variant
LIRI-JP156844658168446581deletion of <=200bpG-intron_variant
LIRI-JP156844814168448141deletion of <=200bpA-downstream_gene_variant
LIRI-JP156844814168448141deletion of <=200bpA-intron_variant
LIRI-JP156844986168449861single base substitutionAGdownstream_gene_variant
LIRI-JP156844986168449861single base substitutionAGintron_variant
LIRI-JP156845246168452461single base substitutionAGintron_variant
LIRI-JP156845617168456171single base substitutionTCintron_variant
LIRI-JP156845731568457315single base substitutionCGintron_variant
LIRI-JP156845862268458622single base substitutionTGintron_variant
LIRI-JP156845967168459671single base substitutionAGintron_variant
LIRI-JP156846427668464276single base substitutionAGintron_variant
LIRI-JP156846427668464276single base substitutionAGupstream_gene_variant
LIRI-JP156846965868469658single base substitutionAGintron_variant
LIRI-JP156846965868469658single base substitutionAGupstream_gene_variant
LIRI-JP156847157768471594deletion of <=200bpTAAATGTAAAACATTTTG-intron_variant
LIRI-JP156847157768471594deletion of <=200bpTAAATGTAAAACATTTTG-upstream_gene_variant
LIRI-JP156847250068472500single base substitutionTAintron_variant
LIRI-JP156847250068472500single base substitutionTAupstream_gene_variant
LIRI-JP156847337568473375single base substitutionAGintron_variant
LIRI-JP156847337568473375single base substitutionAGupstream_gene_variant
LIRI-JP156847350268473502single base substitutionAGintron_variant
LIRI-JP156847350268473502single base substitutionAGupstream_gene_variant
LIRI-JP156847507668475076single base substitutionCTdownstream_gene_variant
LIRI-JP156847507668475076single base substitutionCTintron_variant
LIRI-JP156847832268478322single base substitutionACdownstream_gene_variant
LIRI-JP156847832268478322single base substitutionACintron_variant
LIRI-JP156847930568479305single base substitutionGAintron_variant
LIRI-JP156848214768482147single base substitutionTCdownstream_gene_variant
LIRI-JP156848214768482147single base substitutionTCintron_variant
LIRI-JP156848446468484464single base substitutionAGdownstream_gene_variant
LIRI-JP156848535968485359single base substitutionCAdownstream_gene_variant
LIRI-JP156848614468486144single base substitutionTGdownstream_gene_variant
LIRI-JP156848637968486379single base substitutionTGdownstream_gene_variant
LIRI-JP156848793268487932single base substitutionACdownstream_gene_variant
LIRI-JP156848801768488017single base substitutionACdownstream_gene_variant
LUSC-KR156834210568342105single base substitutionCTupstream_gene_variant
LUSC-KR156834722468347224single base substitutionCG5_prime_UTR_variant
LUSC-KR156834722468347224single base substitutionCGintron_variant
LUSC-KR156835288368352883single base substitutionGAintron_variant
LUSC-KR156836634968366349single base substitutionATintron_variant
LUSC-KR156837475268374752single base substitutionACintron_variant
LUSC-KR156838269668382696single base substitutionATintron_variant
LUSC-KR156838425468384254single base substitutionCGintron_variant
LUSC-KR156839462568394625single base substitutionCGintron_variant
LUSC-KR156839928868399288single base substitutionTCintron_variant
LUSC-KR156840700768407007single base substitutionCTintron_variant
LUSC-KR156841133068411330single base substitutionGCintron_variant
LUSC-KR156841194268411942single base substitutionGTintron_variant
LUSC-KR156842725168427251single base substitutionGAintron_variant
LUSC-KR156842798968427989single base substitutionTCintron_variant
LUSC-KR156842805968428059single base substitutionCAintron_variant
LUSC-KR156843422468434224single base substitutionGTintron_variant
LUSC-KR156843422468434224single base substitutionGTupstream_gene_variant
LUSC-KR156843792468437924single base substitutionCTdownstream_gene_variant
LUSC-KR156843792468437924single base substitutionCTintron_variant
LUSC-KR156843792468437924single base substitutionCTupstream_gene_variant
LUSC-KR156844259268442592single base substitutionAGintron_variant
LUSC-KR156844433468444334single base substitutionCAintron_variant
LUSC-KR156845093468450934single base substitutionCTdownstream_gene_variant
LUSC-KR156845093468450934single base substitutionCTintron_variant
LUSC-KR156845529268455292single base substitutionATintron_variant
LUSC-KR156846722168467221single base substitutionCGintron_variant
LUSC-KR156846722168467221single base substitutionCGupstream_gene_variant
LUSC-KR156846725268467252single base substitutionCGintron_variant
LUSC-KR156846725268467252single base substitutionCGupstream_gene_variant
LUSC-KR156847004468470044single base substitutionAGintron_variant
LUSC-KR156847004468470044single base substitutionAGupstream_gene_variant
LUSC-KR156847214268472142single base substitutionCGintron_variant
LUSC-KR156847214268472142single base substitutionCGupstream_gene_variant
LUSC-KR156847549468475494single base substitutionTCdownstream_gene_variant
LUSC-KR156847549468475494single base substitutionTCintron_variant
LUSC-KR156847619168476191single base substitutionGAdownstream_gene_variant
LUSC-KR156847619168476191single base substitutionGAintron_variant
LUSC-KR156848439768484397single base substitutionCTdownstream_gene_variant
LUSC-US156837891768378917single base substitutionGT3_prime_UTR_variant
LUSC-US156837891768378917single base substitutionGTexon_variant
LUSC-US156837891768378917single base substitutionGTmissense_variantD100Y298G>T
LUSC-US156837891768378917single base substitutionGTmissense_variantD102Y304G>T
LUSC-US156843466968434669single base substitutionAC3_prime_UTR_variant
LUSC-US156843466968434669single base substitutionACmissense_variantQ199P596A>C
LUSC-US156843466968434669single base substitutionACmissense_variantQ201P602A>C
LUSC-US156843466968434669single base substitutionACupstream_gene_variant
LUSC-US156846805868468058single base substitutionCTmissense_variantS418L1253C>T
LUSC-US156846805868468058single base substitutionCTmissense_variantS420L1259C>T
LUSC-US156846805868468058single base substitutionCTupstream_gene_variant
LUSC-US156846806868468068single base substitutionATmissense_variantE421D1263A>T
LUSC-US156846806868468068single base substitutionATmissense_variantE423D1269A>T
LUSC-US156846806868468068single base substitutionATupstream_gene_variant
LUSC-US156847990468479904single base substitutionGTexon_variant
LUSC-US156847990468479904single base substitutionGTmissense_variantA563S1687G>T
LUSC-US156847990468479904single base substitutionGTmissense_variantA565S1693G>T
MALY-DE156834317268343172single base substitutionACupstream_gene_variant
MALY-DE156834841568348415single base substitutionTGintron_variant
MALY-DE156836078768360787single base substitutionGAintron_variant
MALY-DE156836945268369452single base substitutionATintron_variant
MALY-DE156837350068373500single base substitutionATintron_variant
MALY-DE156838040168380401single base substitutionTGintron_variant
MALY-DE156838383168383831single base substitutionCTintron_variant
MALY-DE156838924868389248single base substitutionGTintron_variant
MALY-DE156839067768390677single base substitutionTCintron_variant
MALY-DE156839069968390699single base substitutionTGintron_variant
MALY-DE156839071068390710single base substitutionTAintron_variant
MALY-DE156839699868396998single base substitutionACintron_variant
MALY-DE156839793768397937single base substitutionCTintron_variant
MALY-DE156840671768406717single base substitutionTGintron_variant
MALY-DE156840803268408032single base substitutionGAintron_variant
MALY-DE156840987868409878single base substitutionCTintron_variant
MALY-DE156842290368422903single base substitutionACintron_variant
MALY-DE156842317868423178single base substitutionCGintron_variant
MALY-DE156843076968430769single base substitutionTGintron_variant
MALY-DE156843343068433430single base substitutionAGintron_variant
MALY-DE156843869068438690single base substitutionTGdownstream_gene_variant
MALY-DE156843869068438690single base substitutionTGintron_variant
MALY-DE156843869068438690single base substitutionTGupstream_gene_variant
MALY-DE156843870268438702single base substitutionTAdownstream_gene_variant
MALY-DE156843870268438702single base substitutionTAintron_variant
MALY-DE156843870268438702single base substitutionTAupstream_gene_variant
MALY-DE156846687668466876single base substitutionTGintron_variant
MALY-DE156846687668466876single base substitutionTGupstream_gene_variant
MALY-DE156846924068469240single base substitutionTAintron_variant
MALY-DE156846924068469240single base substitutionTAupstream_gene_variant
MELA-AU156834181168341811single base substitutionGAupstream_gene_variant
MELA-AU156834218168342181single base substitutionCTupstream_gene_variant
MELA-AU156834261668342616single base substitutionCTupstream_gene_variant
MELA-AU156834280368342803single base substitutionAGupstream_gene_variant
MELA-AU156834281268342812single base substitutionCTupstream_gene_variant
MELA-AU156834283068342830single base substitutionTCupstream_gene_variant
MELA-AU156834283268342832single base substitutionCTupstream_gene_variant
MELA-AU156834284168342842multiple base substitution (>=2bp and <=200bp)GATCupstream_gene_variant
MELA-AU156834311068343110single base substitutionCTupstream_gene_variant
MELA-AU156834343768343437single base substitutionGAupstream_gene_variant
MELA-AU156834436768344367single base substitutionGAupstream_gene_variant
MELA-AU156834443168344431single base substitutionGAupstream_gene_variant
MELA-AU156834507568345075single base substitutionGAupstream_gene_variant
MELA-AU156834548168345481single base substitutionCTupstream_gene_variant
MELA-AU156834564568345645single base substitutionCTupstream_gene_variant
MELA-AU156834572668345726single base substitutionGAupstream_gene_variant
MELA-AU156834757668347576single base substitutionGAintron_variant
MELA-AU156834810868348108single base substitutionCTintron_variant
MELA-AU156834844068348440single base substitutionTCintron_variant
MELA-AU156834854768348547single base substitutionTCintron_variant
MELA-AU156835028668350286single base substitutionCTintron_variant
MELA-AU156835043968350439single base substitutionGAintron_variant
MELA-AU156835144468351444single base substitutionAGintron_variant
MELA-AU156835158568351585single base substitutionTGintron_variant
MELA-AU156835187568351875single base substitutionCTintron_variant
MELA-AU156835302368353023single base substitutionACintron_variant
MELA-AU156835323468353234single base substitutionTCintron_variant
MELA-AU156835355868353558single base substitutionCTintron_variant
MELA-AU156835360768353607insertion of <=200bp-CCATintron_variant
MELA-AU156835386868353868single base substitutionAGintron_variant
MELA-AU156835484368354843single base substitutionCTintron_variant
MELA-AU156835492768354928multiple base substitution (>=2bp and <=200bp)GCAAintron_variant
MELA-AU156835683768356837single base substitutionCTintron_variant
MELA-AU156835749168357491single base substitutionCTintron_variant
MELA-AU156835783068357830single base substitutionGAintron_variant
MELA-AU156835809568358095single base substitutionTCintron_variant
MELA-AU156835821468358214single base substitutionGAintron_variant
MELA-AU156835889768358897single base substitutionCTintron_variant
MELA-AU156835912368359123single base substitutionTAintron_variant
MELA-AU156835912768359127single base substitutionGAintron_variant
MELA-AU156835923268359232single base substitutionAGintron_variant
MELA-AU156836019768360197single base substitutionTCintron_variant
MELA-AU156836045168360451single base substitutionCTintron_variant
MELA-AU156836121668361216single base substitutionTCintron_variant
MELA-AU156836181268361812single base substitutionCTintron_variant
MELA-AU156836299968362999single base substitutionCTintron_variant
MELA-AU156836300068363000single base substitutionGAintron_variant
MELA-AU156836349668363496single base substitutionCTintron_variant
MELA-AU156836417168364171single base substitutionACintron_variant
MELA-AU156836479368364793single base substitutionGAintron_variant
MELA-AU156836510768365107single base substitutionCAintron_variant
MELA-AU156836537868365378single base substitutionGAintron_variant
MELA-AU156836600168366001single base substitutionCTintron_variant
MELA-AU156836640468366404single base substitutionGAintron_variant
MELA-AU156836676768366767single base substitutionGTintron_variant
MELA-AU156836797968367979single base substitutionGAintron_variant
MELA-AU156837075168370752multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU156837114368371143single base substitutionAGintron_variant
MELA-AU156837180968371809single base substitutionCTintron_variant
MELA-AU156837317068373170single base substitutionCTintron_variant
MELA-AU156837369768373697single base substitutionTAintron_variant
MELA-AU156837451168374512multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU156837462168374621single base substitutionGTintron_variant
MELA-AU156837513868375138single base substitutionGAintron_variant
MELA-AU156837571268375712single base substitutionCTintron_variant
MELA-AU156837593468375934single base substitutionCTintron_variant
MELA-AU156837593968375939single base substitutionCTintron_variant
MELA-AU156837700668377006single base substitutionCTintron_variant
MELA-AU156837722468377224single base substitutionTCintron_variant
MELA-AU156837728168377281single base substitutionTAintron_variant
MELA-AU156837741668377416single base substitutionCTintron_variant
MELA-AU156838029468380294single base substitutionCAintron_variant
MELA-AU156838051868380518single base substitutionAGintron_variant
MELA-AU156838184468381844single base substitutionCTintron_variant
MELA-AU156838189068381890single base substitutionATintron_variant
MELA-AU156838223268382232single base substitutionATintron_variant
MELA-AU156838254568382545single base substitutionTAintron_variant
MELA-AU156838292868382928single base substitutionGCintron_variant
MELA-AU156838314768383147single base substitutionCTintron_variant
MELA-AU156838341368383413single base substitutionGAintron_variant
MELA-AU156838355368383554multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU156838423268384232single base substitutionCAintron_variant
MELA-AU156838499668385010deletion of <=200bpCCTTATGGATGAGAT-intron_variant
MELA-AU156838525868385258single base substitutionCAintron_variant
MELA-AU156838547968385479single base substitutionCTintron_variant
MELA-AU156838662568386625single base substitutionCTintron_variant
MELA-AU156838694168386941single base substitutionCTintron_variant
MELA-AU156838856168388561single base substitutionGAintron_variant
MELA-AU156838866268388662single base substitutionCTintron_variant
MELA-AU156838888868388888single base substitutionGAintron_variant
MELA-AU156838989468389894single base substitutionCTintron_variant
MELA-AU156838996868389968single base substitutionCTintron_variant
MELA-AU156839008768390087single base substitutionTAintron_variant
MELA-AU156839013268390132single base substitutionCTintron_variant
MELA-AU156839035168390351single base substitutionCAintron_variant
MELA-AU156839076168390761single base substitutionGAintron_variant
MELA-AU156839162568391625single base substitutionCTintron_variant
MELA-AU156839200968392009single base substitutionTCintron_variant
MELA-AU156839326968393269single base substitutionTGintron_variant
MELA-AU156839334168393341single base substitutionCTintron_variant
MELA-AU156839373568393735single base substitutionCTintron_variant
MELA-AU156839411268394112single base substitutionTAintron_variant
MELA-AU156839417168394171single base substitutionCTintron_variant
MELA-AU156839503668395036single base substitutionCTintron_variant
MELA-AU156839604968396049single base substitutionATintron_variant
MELA-AU156839605768396058multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU156839638368396383single base substitutionCTintron_variant
MELA-AU156839670168396701single base substitutionGAintron_variant
MELA-AU156839735268397352single base substitutionCTintron_variant
MELA-AU156839753368397533single base substitutionCTintron_variant
MELA-AU156839761668397616single base substitutionAGintron_variant
MELA-AU156839778968397789single base substitutionCTintron_variant
MELA-AU156839904168399041single base substitutionCTintron_variant
MELA-AU156839915168399151single base substitutionTCintron_variant
MELA-AU156839935368399353single base substitutionCTintron_variant
MELA-AU156839948068399480single base substitutionTCintron_variant
MELA-AU156840024368400243single base substitutionCTintron_variant
MELA-AU156840080868400808single base substitutionCTintron_variant
MELA-AU156840151168401511single base substitutionCTintron_variant
MELA-AU156840293468402934single base substitutionCTintron_variant
MELA-AU156840348968403489single base substitutionCTintron_variant
MELA-AU156840404068404040single base substitutionCTintron_variant
MELA-AU156840471568404715single base substitutionCTintron_variant
MELA-AU156840477068404770single base substitutionGAintron_variant
MELA-AU156840483468404834single base substitutionAGintron_variant
MELA-AU156840487068404870single base substitutionCTintron_variant
MELA-AU156840773568407735single base substitutionGAintron_variant
MELA-AU156840800368408003single base substitutionCTintron_variant
MELA-AU156840844068408440single base substitutionTCintron_variant
MELA-AU156840883768408837single base substitutionGAintron_variant
MELA-AU156840943868409450deletion of <=200bpTCTTGAGACAAAG-intron_variant
MELA-AU156840952068409520single base substitutionGAintron_variant
MELA-AU156840964168409641single base substitutionCTintron_variant
MELA-AU156840994368409943single base substitutionCTintron_variant
MELA-AU156841019068410190single base substitutionCTintron_variant
MELA-AU156841052868410528single base substitutionGAintron_variant
MELA-AU156841054268410542single base substitutionCTintron_variant
MELA-AU156841058868410588single base substitutionGAintron_variant
MELA-AU156841151768411517single base substitutionCTintron_variant
MELA-AU156841282768412827single base substitutionCTintron_variant
MELA-AU156841561668415616single base substitutionCTintron_variant
MELA-AU156841595668415956single base substitutionCTintron_variant
MELA-AU156841710368417103single base substitutionATintron_variant
MELA-AU156841890568418905single base substitutionCTintron_variant
MELA-AU156841962068419620single base substitutionCTintron_variant
MELA-AU156842047268420472single base substitutionGAintron_variant
MELA-AU156842082268420822single base substitutionCTintron_variant
MELA-AU156842121368421213single base substitutionTAintron_variant
MELA-AU156842167968421679single base substitutionGAintron_variant
MELA-AU156842171668421716single base substitutionTCintron_variant
MELA-AU156842243668422436single base substitutionCTintron_variant
MELA-AU156842396968423969single base substitutionAGintron_variant
MELA-AU156842408768424087single base substitutionTCintron_variant
MELA-AU156842529968425299single base substitutionCTintron_variant
MELA-AU156842752668427526single base substitutionGAintron_variant
MELA-AU156842753868427538single base substitutionCTintron_variant
MELA-AU156842841968428419single base substitutionGAintron_variant
MELA-AU156842948168429481single base substitutionCTintron_variant
MELA-AU156842954068429540single base substitutionCTintron_variant
MELA-AU156842960668429606single base substitutionAGintron_variant
MELA-AU156843017668430176single base substitutionCTintron_variant
MELA-AU156843080968430809single base substitutionTAintron_variant
MELA-AU156843148268431482single base substitutionCTintron_variant
MELA-AU156843165568431655single base substitutionGAintron_variant
MELA-AU156843248068432480single base substitutionCTintron_variant
MELA-AU156843251068432510single base substitutionCTintron_variant
MELA-AU156843336168433361single base substitutionATintron_variant
MELA-AU156843396668433966single base substitutionCTintron_variant
MELA-AU156843421468434214single base substitutionTGintron_variant
MELA-AU156843421468434214single base substitutionTGupstream_gene_variant
MELA-AU156843540068435400single base substitutionCTdownstream_gene_variant
MELA-AU156843540068435400single base substitutionCTintron_variant
MELA-AU156843540068435400single base substitutionCTupstream_gene_variant
MELA-AU156843665268436652single base substitutionAGdownstream_gene_variant
MELA-AU156843665268436652single base substitutionAGintron_variant
MELA-AU156843665268436652single base substitutionAGupstream_gene_variant
MELA-AU156843705968437059single base substitutionCTdownstream_gene_variant
MELA-AU156843705968437059single base substitutionCTintron_variant
MELA-AU156843705968437059single base substitutionCTupstream_gene_variant
MELA-AU156843709468437094single base substitutionTAdownstream_gene_variant
MELA-AU156843709468437094single base substitutionTAintron_variant
MELA-AU156843709468437094single base substitutionTAupstream_gene_variant
MELA-AU156843710268437102single base substitutionCTdownstream_gene_variant
MELA-AU156843710268437102single base substitutionCTintron_variant
MELA-AU156843710268437102single base substitutionCTupstream_gene_variant
MELA-AU156843761868437618single base substitutionCTdownstream_gene_variant
MELA-AU156843761868437618single base substitutionCTintron_variant
MELA-AU156843761868437618single base substitutionCTupstream_gene_variant
MELA-AU156843795568437955single base substitutionAGdownstream_gene_variant
MELA-AU156843795568437955single base substitutionAGintron_variant
MELA-AU156843795568437955single base substitutionAGupstream_gene_variant
MELA-AU156843900568439005single base substitutionGAdownstream_gene_variant
MELA-AU156843900568439005single base substitutionGAexon_variant
MELA-AU156843900568439005single base substitutionGAsynonymous_variantT265T795G>A
MELA-AU156843900568439005single base substitutionGAsynonymous_variantT267T801G>A
MELA-AU156844156368441563single base substitutionATintron_variant
MELA-AU156844184768441847single base substitutionGTintron_variant
MELA-AU156844242168442421single base substitutionCTintron_variant
MELA-AU156844242168442422multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU156844267668442676single base substitutionCTintron_variant
MELA-AU156844401668444016single base substitutionACintron_variant
MELA-AU156844404368444043single base substitutionCAintron_variant
MELA-AU156844408568444085single base substitutionTCintron_variant
MELA-AU156844419368444193single base substitutionGAintron_variant
MELA-AU156844451468444514single base substitutionCTintron_variant
MELA-AU156844479268444792single base substitutionCTintron_variant
MELA-AU156844508768445087single base substitutionCTintron_variant
MELA-AU156844556268445562single base substitutionATintron_variant
MELA-AU156844560068445600single base substitutionCTintron_variant
MELA-AU156844580368445803single base substitutionGTintron_variant
MELA-AU156844650668446506single base substitutionCTdownstream_gene_variant
MELA-AU156844650668446506single base substitutionCTintron_variant
MELA-AU156844806768448067single base substitutionTCdownstream_gene_variant
MELA-AU156844806768448067single base substitutionTCintron_variant
MELA-AU156844839368448393single base substitutionCTdownstream_gene_variant
MELA-AU156844839368448393single base substitutionCTintron_variant
MELA-AU156844850268448502single base substitutionCTdownstream_gene_variant
MELA-AU156844850268448502single base substitutionCTintron_variant
MELA-AU156844887668448876single base substitutionCTdownstream_gene_variant
MELA-AU156844887668448876single base substitutionCTintron_variant
MELA-AU156844906168449061single base substitutionATdownstream_gene_variant
MELA-AU156844906168449061single base substitutionATintron_variant
MELA-AU156844917568449175single base substitutionTAdownstream_gene_variant
MELA-AU156844917568449175single base substitutionTAintron_variant
MELA-AU156844966168449661single base substitutionTCdownstream_gene_variant
MELA-AU156844966168449661single base substitutionTCintron_variant
MELA-AU156844994668449946single base substitutionTAdownstream_gene_variant
MELA-AU156844994668449946single base substitutionTAintron_variant
MELA-AU156845043068450430single base substitutionCTdownstream_gene_variant
MELA-AU156845043068450430single base substitutionCTintron_variant
MELA-AU156845043168450431single base substitutionCTdownstream_gene_variant
MELA-AU156845043168450431single base substitutionCTintron_variant
MELA-AU156845150768451507single base substitutionCTintron_variant
MELA-AU156845180368451803single base substitutionCTintron_variant
MELA-AU156845278968452789single base substitutionCTintron_variant
MELA-AU156845309168453091single base substitutionAGintron_variant
MELA-AU156845337168453371single base substitutionCTintron_variant
MELA-AU156845347368453473single base substitutionAGintron_variant
MELA-AU156845406168454061single base substitutionGTintron_variant
MELA-AU156845444868454448single base substitutionTAintron_variant
MELA-AU156845464868454648single base substitutionCTintron_variant
MELA-AU156845505668455056single base substitutionCTintron_variant
MELA-AU156845506368455063single base substitutionCTintron_variant
MELA-AU156845525668455256single base substitutionCTintron_variant
MELA-AU156845528168455281single base substitutionCTintron_variant
MELA-AU156845644768456447single base substitutionCTintron_variant
MELA-AU156846052668460526single base substitutionCTintron_variant
MELA-AU156846067468460674single base substitutionCTintron_variant
MELA-AU156846067968460679single base substitutionCTintron_variant
MELA-AU156846073868460738single base substitutionTCintron_variant
MELA-AU156846151568461515single base substitutionTCintron_variant
MELA-AU156846169868461698single base substitutionCTintron_variant
MELA-AU156846240968462409single base substitutionCTintron_variant
MELA-AU156846378768463787single base substitutionTCintron_variant
MELA-AU156846413368464133single base substitutionCTintron_variant
MELA-AU156846413368464133single base substitutionCTupstream_gene_variant
MELA-AU156846447068464470single base substitutionCTintron_variant
MELA-AU156846447068464470single base substitutionCTupstream_gene_variant
MELA-AU156846464968464649single base substitutionCTintron_variant
MELA-AU156846464968464649single base substitutionCTupstream_gene_variant
MELA-AU156846475668464756single base substitutionCAintron_variant
MELA-AU156846475668464756single base substitutionCAupstream_gene_variant
MELA-AU156846481768464817single base substitutionTCintron_variant
MELA-AU156846481768464817single base substitutionTCupstream_gene_variant
MELA-AU156846511868465119multiple base substitution (>=2bp and <=200bp)CTTCintron_variant
MELA-AU156846511868465119multiple base substitution (>=2bp and <=200bp)CTTCupstream_gene_variant
MELA-AU156846587268465872single base substitutionTCintron_variant
MELA-AU156846587268465872single base substitutionTCupstream_gene_variant
MELA-AU156846637968466379single base substitutionCTintron_variant
MELA-AU156846637968466379single base substitutionCTupstream_gene_variant
MELA-AU156846652368466523single base substitutionCTintron_variant
MELA-AU156846652368466523single base substitutionCTupstream_gene_variant
MELA-AU156846738968467389single base substitutionCTintron_variant
MELA-AU156846738968467389single base substitutionCTupstream_gene_variant
MELA-AU156846854968468549single base substitutionCTintron_variant
MELA-AU156846854968468549single base substitutionCTupstream_gene_variant
MELA-AU156846869368468693single base substitutionAGintron_variant
MELA-AU156846869368468693single base substitutionAGupstream_gene_variant
MELA-AU156846885668468856single base substitutionCTstop_gainedQ449*1345C>T
MELA-AU156846885668468856single base substitutionCTstop_gainedQ451*1351C>T
MELA-AU156846885668468856single base substitutionCTupstream_gene_variant
MELA-AU156846899168468991single base substitutionGAmissense_variantG494S1480G>A
MELA-AU156846899168468991single base substitutionGAmissense_variantG496S1486G>A
MELA-AU156846899168468991single base substitutionGAsplice_region_variant
MELA-AU156846899168468991single base substitutionGAupstream_gene_variant
MELA-AU156846953168469531single base substitutionCTintron_variant
MELA-AU156846953168469531single base substitutionCTupstream_gene_variant
MELA-AU156846958568469585single base substitutionCTintron_variant
MELA-AU156846958568469585single base substitutionCTupstream_gene_variant
MELA-AU156847034768470347single base substitutionGCintron_variant
MELA-AU156847034768470347single base substitutionGCupstream_gene_variant
MELA-AU156847093368470933single base substitutionCTintron_variant
MELA-AU156847093368470933single base substitutionCTupstream_gene_variant
MELA-AU156847101168471011single base substitutionCTintron_variant
MELA-AU156847101168471011single base substitutionCTupstream_gene_variant
MELA-AU156847217968472179single base substitutionGAintron_variant
MELA-AU156847217968472179single base substitutionGAupstream_gene_variant
MELA-AU156847231368472313single base substitutionCTintron_variant
MELA-AU156847231368472313single base substitutionCTupstream_gene_variant
MELA-AU156847277168472771single base substitutionCTintron_variant
MELA-AU156847277168472771single base substitutionCTupstream_gene_variant
MELA-AU156847280568472805single base substitutionTAintron_variant
MELA-AU156847280568472805single base substitutionTAupstream_gene_variant
MELA-AU156847288268472882single base substitutionCTintron_variant
MELA-AU156847288268472882single base substitutionCTupstream_gene_variant
MELA-AU156847380368473803single base substitutionCTexon_variant
MELA-AU156847380368473803single base substitutionCTintron_variant
MELA-AU156847420568474205single base substitutionGAexon_variant
MELA-AU156847420568474205single base substitutionGAintron_variant
MELA-AU156847551368475513single base substitutionAGdownstream_gene_variant
MELA-AU156847551368475513single base substitutionAGintron_variant
MELA-AU156847710168477102multiple base substitution (>=2bp and <=200bp)TAATdownstream_gene_variant
MELA-AU156847710168477102multiple base substitution (>=2bp and <=200bp)TAATintron_variant
MELA-AU156847719368477193single base substitutionCTdownstream_gene_variant
MELA-AU156847719368477193single base substitutionCTintron_variant
MELA-AU156847726768477267single base substitutionGAdownstream_gene_variant
MELA-AU156847726768477267single base substitutionGAintron_variant
MELA-AU156847804968478049single base substitutionCTdownstream_gene_variant
MELA-AU156847804968478049single base substitutionCTintron_variant
MELA-AU156847957668479576single base substitutionTAintron_variant
MELA-AU156847986068479860single base substitutionCTintron_variant
MELA-AU156848052868480528single base substitutionGA3_prime_UTR_variant
MELA-AU156848052868480528single base substitutionGAdownstream_gene_variant
MELA-AU156848204268482042single base substitutionCTdownstream_gene_variant
MELA-AU156848204268482042single base substitutionCTintron_variant
MELA-AU156848337068483370single base substitutionGAdownstream_gene_variant
MELA-AU156848352868483528single base substitutionATdownstream_gene_variant
MELA-AU156848384168483841single base substitutionGAdownstream_gene_variant
MELA-AU156848599568485995single base substitutionGAdownstream_gene_variant
ORCA-IN156839573468395734single base substitutionAGintron_variant
ORCA-IN156840121368401213single base substitutionCTintron_variant
ORCA-IN156840713868407138single base substitutionTCintron_variant
ORCA-IN156842055368420553single base substitutionGAintron_variant
ORCA-IN156845195868451958single base substitutionTGintron_variant
OV-AU156834281468342814single base substitutionTCupstream_gene_variant
OV-AU156834281668342816single base substitutionTCupstream_gene_variant
OV-AU156834283168342831single base substitutionATupstream_gene_variant
OV-AU156835272868352728single base substitutionAGintron_variant
OV-AU156835290668352906single base substitutionGAintron_variant
OV-AU156837810968378109single base substitutionGAintron_variant
OV-AU156841458568414585single base substitutionGTintron_variant
OV-AU156841645268416452single base substitutionAGintron_variant
OV-AU156842181468421814single base substitutionTGintron_variant
OV-AU156842941768429417single base substitutionAGintron_variant
OV-AU156843038968430389single base substitutionGCintron_variant
OV-AU156843937868439378single base substitutionGAdownstream_gene_variant
OV-AU156843937868439378single base substitutionGAintron_variant
OV-AU156844612868446128single base substitutionCTexon_variant
OV-AU156844612868446128single base substitutionCTintron_variant
OV-AU156845234968452349single base substitutionCGintron_variant
OV-AU156847723268477232single base substitutionGAdownstream_gene_variant
OV-AU156847723268477232single base substitutionGAintron_variant
OV-AU156847949868479498single base substitutionGCintron_variant
OV-AU156848298868482988single base substitutionGA3_prime_UTR_variant
OV-AU156848298868482988single base substitutionGAdownstream_gene_variant
OV-US156843429168434291single base substitutionCT3_prime_UTR_variant
OV-US156843429168434291single base substitutionCTsynonymous_variantD159D477C>T
OV-US156843429168434291single base substitutionCTsynonymous_variantD161D483C>T
OV-US156843429168434291single base substitutionCTupstream_gene_variant
PACA-AU156834283168342831single base substitutionATupstream_gene_variant
PACA-AU156834304768343047single base substitutionTCupstream_gene_variant
PACA-AU156834757468347598deletion of <=200bpATGGTTCGTGTTTATATCCCCCCAT-intron_variant
PACA-AU156835055468350554single base substitutionCAintron_variant
PACA-AU156835730268357302single base substitutionCTintron_variant
PACA-AU156835925768359257single base substitutionTAintron_variant
PACA-AU156836834168368341single base substitutionGAintron_variant
PACA-AU156837060768370607single base substitutionTAintron_variant
PACA-AU156837060968370609single base substitutionTAintron_variant
PACA-AU156838051868380518single base substitutionAGintron_variant
PACA-AU156838536868385368single base substitutionGAintron_variant
PACA-AU156838619268386192insertion of <=200bp-Tintron_variant
PACA-AU156839328168393281single base substitutionTGintron_variant
PACA-AU156840608568406085single base substitutionGTintron_variant
PACA-AU156840924368409243single base substitutionTGintron_variant
PACA-AU156841821368418213insertion of <=200bp-Tintron_variant
PACA-AU156842025768420257single base substitutionCTintron_variant
PACA-AU156842026868420268single base substitutionTAintron_variant
PACA-AU156845762768457627deletion of <=200bpT-intron_variant
PACA-AU156845883568458835single base substitutionTCintron_variant
PACA-AU156846002968460029single base substitutionGCintron_variant
PACA-AU156846097368460973single base substitutionCTintron_variant
PACA-AU156846611368466113single base substitutionGAmissense_variantC351Y1052G>A
PACA-AU156846611368466113single base substitutionGAmissense_variantC353Y1058G>A
PACA-AU156846611368466113single base substitutionGAupstream_gene_variant
PACA-AU156847445668474456single base substitutionATdownstream_gene_variant
PACA-AU156847445668474456single base substitutionATintron_variant
PACA-AU156847704968477049single base substitutionCTdownstream_gene_variant
PACA-AU156847704968477049single base substitutionCTintron_variant
PACA-AU156847745868477458single base substitutionCTdownstream_gene_variant
PACA-AU156847745868477458single base substitutionCTintron_variant
PACA-AU156847800168478001single base substitutionATdownstream_gene_variant
PACA-AU156847800168478001single base substitutionATintron_variant
PACA-AU156848770668487706single base substitutionTAdownstream_gene_variant
PACA-CA156834228068342280single base substitutionAGupstream_gene_variant
PACA-CA156834368668343686single base substitutionTCupstream_gene_variant
PACA-CA156834639568346396deletion of <=200bpGG-upstream_gene_variant
PACA-CA156834767768347677single base substitutionACintron_variant
PACA-CA156834853168348531single base substitutionAGintron_variant
PACA-CA156835751168357512deletion of <=200bpAG-intron_variant
PACA-CA156836497968364979single base substitutionCTintron_variant
PACA-CA156837042268370422single base substitutionGAintron_variant
PACA-CA156837722568377225single base substitutionCTintron_variant
PACA-CA156839155868391558single base substitutionCTintron_variant
PACA-CA156839213868392138insertion of <=200bp-Tintron_variant
PACA-CA156839283568392835single base substitutionGAintron_variant
PACA-CA156839541268395412single base substitutionCTintron_variant
PACA-CA156839637268396372single base substitutionCTintron_variant
PACA-CA156839908668399086single base substitutionGTintron_variant
PACA-CA156840297168402971single base substitutionGAintron_variant
PACA-CA156841381268413812insertion of <=200bp-Tintron_variant
PACA-CA156842249168422491single base substitutionTCintron_variant
PACA-CA156843036368430363single base substitutionTCintron_variant
PACA-CA156843725268437252single base substitutionGAdownstream_gene_variant
PACA-CA156843725268437252single base substitutionGAintron_variant
PACA-CA156843725268437252single base substitutionGAupstream_gene_variant
PACA-CA156845255268452552single base substitutionAGintron_variant
PACA-CA156845281268452812single base substitutionAGintron_variant
PACA-CA156845784468457844single base substitutionTCintron_variant
PACA-CA156846106068461071deletion of <=200bpTTTATGATTCTA-intron_variant
PACA-CA156846279368462810deletion of <=200bpTGTATGGGGCACTTACTA-intron_variant
PACA-CA156847439468474396deletion of <=200bpTGG-downstream_gene_variant
PACA-CA156847439468474396deletion of <=200bpTGG-intron_variant
PACA-CA156847654068476540single base substitutionCGdownstream_gene_variant
PACA-CA156847654068476540single base substitutionCGintron_variant
PACA-CA156847664268476642single base substitutionCGdownstream_gene_variant
PACA-CA156847664268476642single base substitutionCGintron_variant
PACA-CA156848623668486236single base substitutionGCdownstream_gene_variant
PAEN-AU156834277168342771insertion of <=200bp-ATupstream_gene_variant
PAEN-AU156834281468342814single base substitutionTCupstream_gene_variant
PAEN-AU156837062868370628single base substitutionGTintron_variant
PAEN-AU156838142168381421single base substitutionTGintron_variant
PAEN-AU156839834968398349single base substitutionCAintron_variant
PAEN-AU156841336068413360single base substitutionCAintron_variant
PAEN-AU156842932168429321single base substitutionCAintron_variant
PAEN-AU156846738768467387single base substitutionTCintron_variant
PAEN-AU156846738768467387single base substitutionTCupstream_gene_variant
PAEN-AU156847181168471811single base substitutionACintron_variant
PAEN-AU156847181168471811single base substitutionACupstream_gene_variant
PAEN-IT156839253768392537single base substitutionCAintron_variant
PAEN-IT156846947868469478single base substitutionGAintron_variant
PAEN-IT156846947868469478single base substitutionGAupstream_gene_variant
PAEN-IT156847117168471171single base substitutionCAintron_variant
PAEN-IT156847117168471171single base substitutionCAupstream_gene_variant
PBCA-DE156834230768342307single base substitutionCTupstream_gene_variant
PBCA-DE156834657168346571single base substitutionAG5_prime_UTR_variant
PBCA-DE156834657168346571single base substitutionAGupstream_gene_variant
PBCA-DE156835821368358213insertion of <=200bp-Gintron_variant
PBCA-DE156836355768363557single base substitutionTCintron_variant
PBCA-DE156836411668364116single base substitutionCTintron_variant
PBCA-DE156836952068369520single base substitutionAGintron_variant
PBCA-DE156838495568384955single base substitutionGTintron_variant
PBCA-DE156838652768386527single base substitutionACintron_variant
PBCA-DE156838802668388026single base substitutionGAintron_variant
PBCA-DE156839352868393528single base substitutionGAintron_variant
PBCA-DE156840288068402880single base substitutionGTintron_variant
PBCA-DE156840654368406543single base substitutionCTintron_variant
PBCA-DE156842144468421444deletion of <=200bpG-intron_variant
PBCA-DE156843443668434436single base substitutionACintron_variant
PBCA-DE156843443668434436single base substitutionACupstream_gene_variant
PBCA-DE156843541368435414deletion of <=200bpAT-downstream_gene_variant
PBCA-DE156843541368435414deletion of <=200bpAT-intron_variant
PBCA-DE156843541368435414deletion of <=200bpAT-upstream_gene_variant
PBCA-DE156844702168447033deletion of <=200bpATTAAAATGGTCC-downstream_gene_variant
PBCA-DE156844702168447033deletion of <=200bpATTAAAATGGTCC-intron_variant
PBCA-DE156845953068459531deletion of <=200bpTG-intron_variant
PBCA-DE156847290168472901single base substitutionTAintron_variant
PBCA-DE156847290168472901single base substitutionTAupstream_gene_variant
PBCA-DE156848309768483097insertion of <=200bp-Adownstream_gene_variant
PRAD-CA156834278468342784single base substitutionCTupstream_gene_variant
PRAD-CA156834278568342785single base substitutionGAupstream_gene_variant
PRAD-CA156835274968352749single base substitutionGAintron_variant
PRAD-CA156836451168364511single base substitutionCTintron_variant
PRAD-CA156838711468387114single base substitutionACintron_variant
PRAD-CA156838924868389248single base substitutionGTintron_variant
PRAD-CA156839666768396667single base substitutionTAintron_variant
PRAD-CA156841067268410672single base substitutionATintron_variant
PRAD-CA156843257168432571single base substitutionCAintron_variant
PRAD-CA156844741268447412single base substitutionGAdownstream_gene_variant
PRAD-CA156844741268447412single base substitutionGAintron_variant
PRAD-CA156847806068478060single base substitutionGCdownstream_gene_variant
PRAD-CA156847806068478060single base substitutionGCintron_variant
PRAD-UK156834571468345715deletion of <=200bpTA-upstream_gene_variant
PRAD-UK156834818368348183single base substitutionTA5_prime_UTR_variant
PRAD-UK156834818368348183single base substitutionTAintron_variant
PRAD-UK156836530468365304single base substitutionCGintron_variant
PRAD-UK156836778468367784single base substitutionCTintron_variant
PRAD-UK156839351368393513single base substitutionCTintron_variant
PRAD-UK156839719368397193single base substitutionAGintron_variant
PRAD-UK156840719568407195single base substitutionCTintron_variant
PRAD-UK156841880768418807single base substitutionATintron_variant
PRAD-UK156842036068420360single base substitutionCTintron_variant
PRAD-UK156843553168435531single base substitutionTCdownstream_gene_variant
PRAD-UK156843553168435531single base substitutionTCintron_variant
PRAD-UK156843553168435531single base substitutionTCupstream_gene_variant
PRAD-UK156845598268455982single base substitutionGAintron_variant
PRAD-UK156845774968457749single base substitutionGAintron_variant
PRAD-UK156846873368468733single base substitutionTGintron_variant
PRAD-UK156846873368468733single base substitutionTGupstream_gene_variant
READ-US156837871768378717single base substitutionGA3_prime_UTR_variant
READ-US156837871768378717single base substitutionGAexon_variant
READ-US156837871768378717single base substitutionGAmissense_variantR33H98G>A
READ-US156837871768378717single base substitutionGAmissense_variantR35H104G>A
RECA-EU156834162368341623single base substitutionACupstream_gene_variant
RECA-EU156835156968351569single base substitutionTAintron_variant
RECA-EU156835248568352485single base substitutionTCintron_variant
RECA-EU156835836068358360single base substitutionGAintron_variant
RECA-EU156837385968373859single base substitutionAGintron_variant
RECA-EU156838195568381955single base substitutionCAintron_variant
RECA-EU156838408768384087single base substitutionATintron_variant
RECA-EU156838575068385750single base substitutionCTintron_variant
RECA-EU156838590168385901single base substitutionTGintron_variant
RECA-EU156838966868389668single base substitutionTCintron_variant
RECA-EU156839078368390783single base substitutionGCintron_variant
RECA-EU156839915268399152single base substitutionTCintron_variant
RECA-EU156841090468410904single base substitutionTCintron_variant
RECA-EU156841638068416380single base substitutionGAintron_variant
RECA-EU156842105268421052single base substitutionAGintron_variant
RECA-EU156843236568432365single base substitutionACintron_variant
RECA-EU156843402168434021single base substitutionAGintron_variant
RECA-EU156843402168434021single base substitutionAGupstream_gene_variant
RECA-EU156845576068455760single base substitutionAGintron_variant
RECA-EU156845923868459238single base substitutionAGintron_variant
RECA-EU156847660768476607single base substitutionCAdownstream_gene_variant
RECA-EU156847660768476607single base substitutionCAintron_variant
RECA-EU156847971668479716single base substitutionTAintron_variant
RECA-EU156848644768486447single base substitutionTGdownstream_gene_variant
RECA-EU156848754968487549single base substitutionTAdownstream_gene_variant
SKCA-BR156834219368342193single base substitutionGAupstream_gene_variant
SKCA-BR156834281268342812insertion of <=200bp-CATupstream_gene_variant
SKCA-BR156834282268342822insertion of <=200bp-CATupstream_gene_variant
SKCA-BR156834454468344544single base substitutionGAupstream_gene_variant
SKCA-BR156834494468344944single base substitutionGAupstream_gene_variant
SKCA-BR156834659468346594single base substitutionGA5_prime_UTR_variant
SKCA-BR156834659468346594single base substitutionGAupstream_gene_variant
SKCA-BR156834722468347224single base substitutionCT5_prime_UTR_premature_start_codon_gain_variant
SKCA-BR156834722468347224single base substitutionCTintron_variant
SKCA-BR156834847068348470single base substitutionGAintron_variant
SKCA-BR156834863668348636single base substitutionGAintron_variant
SKCA-BR156835204768352047insertion of <=200bp-CAintron_variant
SKCA-BR156835792368357923single base substitutionCTintron_variant
SKCA-BR156836251668362516single base substitutionCTintron_variant
SKCA-BR156836327568363275single base substitutionTGintron_variant
SKCA-BR156836415468364154single base substitutionCTintron_variant
SKCA-BR156836463568364635single base substitutionGAintron_variant
SKCA-BR156836463668364636single base substitutionTGintron_variant
SKCA-BR156836559068365590single base substitutionCTintron_variant
SKCA-BR156836740868367408single base substitutionCTintron_variant
SKCA-BR156836741768367417insertion of <=200bp-TTTCintron_variant
SKCA-BR156836761768367617single base substitutionTGintron_variant
SKCA-BR156837375268373752single base substitutionCTintron_variant
SKCA-BR156838051468380514insertion of <=200bp-GTGTATATATATATATATATAintron_variant
SKCA-BR156838051668380516single base substitutionAGintron_variant
SKCA-BR156838326568383265insertion of <=200bp-GGAGTGTintron_variant
SKCA-BR156838567768385677single base substitutionCTintron_variant
SKCA-BR156838786568387865single base substitutionCTintron_variant
SKCA-BR156838960468389604single base substitutionCTintron_variant
SKCA-BR156839036068390360single base substitutionTAintron_variant
SKCA-BR156839243668392438deletion of <=200bpGAA-intron_variant
SKCA-BR156839561168395611insertion of <=200bp-ATintron_variant
SKCA-BR156839712868397128single base substitutionAGintron_variant
SKCA-BR156839829368398293single base substitutionATintron_variant
SKCA-BR156840109268401092single base substitutionGAintron_variant
SKCA-BR156840243268402432single base substitutionCTintron_variant
SKCA-BR156840348168403481single base substitutionGAintron_variant
SKCA-BR156841614668416146single base substitutionGAintron_variant
SKCA-BR156841674468416744insertion of <=200bp-GTintron_variant
SKCA-BR156842034868420348single base substitutionGAintron_variant
SKCA-BR156842161368421613single base substitutionCTintron_variant
SKCA-BR156842217868422178single base substitutionTCintron_variant
SKCA-BR156842299468422994single base substitutionAGintron_variant
SKCA-BR156842300568423005insertion of <=200bp-TAintron_variant
SKCA-BR156842437368424373insertion of <=200bp-TAintron_variant
SKCA-BR156842438368424389deletion of <=200bpAAAAAAG-intron_variant
SKCA-BR156842696968426969single base substitutionACintron_variant
SKCA-BR156842698368426983single base substitutionCAintron_variant
SKCA-BR156843225168432251insertion of <=200bp-ATintron_variant
SKCA-BR156843719768437197single base substitutionTAdownstream_gene_variant
SKCA-BR156843719768437197single base substitutionTAintron_variant
SKCA-BR156843719768437197single base substitutionTAupstream_gene_variant
SKCA-BR156843763468437634single base substitutionAGdownstream_gene_variant
SKCA-BR156843763468437634single base substitutionAGintron_variant
SKCA-BR156843763468437634single base substitutionAGupstream_gene_variant
SKCA-BR156843981168439811single base substitutionTCintron_variant
SKCA-BR156844907168449071single base substitutionGAdownstream_gene_variant
SKCA-BR156844907168449071single base substitutionGAintron_variant
SKCA-BR156845991668459916single base substitutionCTintron_variant
SKCA-BR156846936568469365single base substitutionCTintron_variant
SKCA-BR156846936568469365single base substitutionCTupstream_gene_variant
SKCA-BR156846964068469640single base substitutionGAintron_variant
SKCA-BR156846964068469640single base substitutionGAupstream_gene_variant
SKCA-BR156847189168471891single base substitutionCTintron_variant
SKCA-BR156847189168471891single base substitutionCTupstream_gene_variant
SKCA-BR156847190268471912deletion of <=200bpCTTTTTTTTTT-intron_variant
SKCA-BR156847190268471912deletion of <=200bpCTTTTTTTTTT-upstream_gene_variant
SKCA-BR156847295468472954insertion of <=200bp-ACATTintron_variant
SKCA-BR156847295468472954insertion of <=200bp-ACATTupstream_gene_variant
SKCA-BR156847383668473836single base substitutionCTexon_variant
SKCA-BR156847383668473836single base substitutionCTintron_variant
SKCA-BR156847848468478484single base substitutionGCdownstream_gene_variant
SKCA-BR156847848468478484single base substitutionGCintron_variant
SKCA-BR156848623868486238single base substitutionTAdownstream_gene_variant
SKCA-BR156848672268486723deletion of <=200bpCT-downstream_gene_variant
SKCM-US156837901668379016single base substitutionCT3_prime_UTR_variant
SKCM-US156837901668379016single base substitutionCTexon_variant
SKCM-US156837901668379016single base substitutionCTmissense_variantH133Y397C>T
SKCM-US156837901668379016single base substitutionCTmissense_variantH135Y403C>T
SKCM-US156844597968445979single base substitutionCTexon_variant
SKCM-US156844597968445979single base substitutionCTmissense_variantL294F880C>T
SKCM-US156844597968445979single base substitutionCTmissense_variantL296F886C>T
SKCM-US156846899168468991single base substitutionGAmissense_variantG494S1480G>A
SKCM-US156846899168468991single base substitutionGAmissense_variantG496S1486G>A
SKCM-US156846899168468991single base substitutionGAsplice_region_variant
SKCM-US156846899168468991single base substitutionGAupstream_gene_variant
STAD-US156837887568378875single base substitutionCA3_prime_UTR_variant
STAD-US156837887568378875single base substitutionCAexon_variant
STAD-US156837887568378875single base substitutionCAmissense_variantP86T256C>A
STAD-US156837887568378875single base substitutionCAmissense_variantP88T262C>A
STAD-US156843892168438921deletion of <=200bpA-downstream_gene_variant
STAD-US156843892168438921deletion of <=200bpA-frameshift_variantT237
STAD-US156843892168438921deletion of <=200bpA-frameshift_variantT239
STAD-US156843892168438921deletion of <=200bpA-upstream_gene_variant
STAD-US156843893068438930single base substitutionCTdownstream_gene_variant
STAD-US156843893068438930single base substitutionCTsynonymous_variantG240G720C>T
STAD-US156843893068438930single base substitutionCTsynonymous_variantG242G726C>T
STAD-US156843893068438930single base substitutionCTupstream_gene_variant
STAD-US156843895268438952single base substitutionCTdownstream_gene_variant
STAD-US156843895268438952single base substitutionCTstop_gainedR248*742C>T
STAD-US156843895268438952single base substitutionCTstop_gainedR250*748C>T
STAD-US156843895268438952single base substitutionCTupstream_gene_variant
STAD-US156843896868438968single base substitutionCTdownstream_gene_variant
STAD-US156843896868438968single base substitutionCTmissense_variantT253I758C>T
STAD-US156843896868438968single base substitutionCTmissense_variantT255I764C>T
STAD-US156843896868438968single base substitutionCTupstream_gene_variant
STAD-US156844596368445963single base substitutionGAexon_variant
STAD-US156844596368445963single base substitutionGAsynonymous_variantL288L864G>A
STAD-US156844596368445963single base substitutionGAsynonymous_variantL290L870G>A
STAD-US156844598968445989single base substitutionTCexon_variant
STAD-US156844598968445989single base substitutionTCmissense_variantL297S890T>C
STAD-US156844598968445989single base substitutionTCmissense_variantL299S896T>C
STAD-US156844599268445992single base substitutionGAexon_variant
STAD-US156844599268445992single base substitutionGAmissense_variantR298Q893G>A
STAD-US156844599268445992single base substitutionGAmissense_variantR300Q899G>A
STAD-US156846613568466135single base substitutionCTsynonymous_variantD358D1074C>T
STAD-US156846613568466135single base substitutionCTsynonymous_variantD360D1080C>T
STAD-US156846613568466135single base substitutionCTupstream_gene_variant
STAD-US156846805968468059deletion of <=200bpA-frameshift_variantS418
STAD-US156846805968468059deletion of <=200bpA-frameshift_variantS420
STAD-US156846805968468059deletion of <=200bpA-upstream_gene_variant
STAD-US156847989068479892deletion of <=200bpCCT-exon_variant
STAD-US156847989068479892deletion of <=200bpCCT-inframe_deletionTS558T
STAD-US156847989068479892deletion of <=200bpCCT-inframe_deletionTS560T
STAD-US156847994668479946single base substitutionTC3_prime_UTR_variant
STAD-US156847994668479946single base substitutionTCmissense_variantS577P1729T>C
STAD-US156847994668479946single base substitutionTCmissense_variantS579P1735T>C
STAD-US156847995568479955deletion of <=200bpT-3_prime_UTR_variant
STAD-US156847995568479955deletion of <=200bpT-frameshift_variantF580
STAD-US156847995568479955deletion of <=200bpT-frameshift_variantF582
UCEC-US156837883268378832single base substitutionGA3_prime_UTR_variant
UCEC-US156837883268378832single base substitutionGAexon_variant
UCEC-US156837883268378832single base substitutionGAsynonymous_variantT71T213G>A
UCEC-US156837883268378832single base substitutionGAsynonymous_variantT73T219G>A
UCEC-US156837883968378839single base substitutionGA3_prime_UTR_variant
UCEC-US156837883968378839single base substitutionGAexon_variant
UCEC-US156837883968378839single base substitutionGAmissense_variantD74N220G>A
UCEC-US156837883968378839single base substitutionGAmissense_variantD76N226G>A
UCEC-US156837900768379007single base substitutionCA3_prime_UTR_variant
UCEC-US156837900768379007single base substitutionCAexon_variant
UCEC-US156837900768379007single base substitutionCAmissense_variantH130N388C>A
UCEC-US156837900768379007single base substitutionCAmissense_variantH132N394C>A
UCEC-US156843429368434293single base substitutionAG3_prime_UTR_variant
UCEC-US156843429368434293single base substitutionAGmissense_variantN160S479A>G
UCEC-US156843429368434293single base substitutionAGmissense_variantN162S485A>G
UCEC-US156843429368434293single base substitutionAGupstream_gene_variant
UCEC-US156846622068466220single base substitutionAGmissense_variantI387V1159A>G
UCEC-US156846622068466220single base substitutionAGmissense_variantI389V1165A>G
UCEC-US156846622068466220single base substitutionAGupstream_gene_variant
UCEC-US156847357968473579single base substitutionCTexon_variant
UCEC-US156847357968473579single base substitutionCTmissense_variantP504L1511C>T
UCEC-US156847357968473579single base substitutionCTmissense_variantP506L1517C>T
UCEC-US156847368368473683single base substitutionGAexon_variant
UCEC-US156847368368473683single base substitutionGAmissense_variantD539N1615G>A
UCEC-US156847368368473683single base substitutionGAmissense_variantD541N1621G>A
UCEC-US156847596768475967single base substitutionGAdownstream_gene_variant
UCEC-US156847596768475967single base substitutionGAintron_variant
UCEC-US156847596768475967single base substitutionGAsplice_acceptor_variant
UCEC-US156848644268486442single base substitutionGTdownstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
sysucc-880TCOSM5462475c.531A>Gp.Q177QSubstitution - coding silent15:68142007-68142007+
TCGA-06-0644-01COSM2151240c.1330G>Tp.V444LSubstitution - Missense15:68176503-68176503+
TCGA-AF-A56N-01COSM5066440c.1456C>Tp.P486SSubstitution - Missense15:68176629-68176629+
2250206COSM5030375c.1267C>Tp.Q423*Substitution - Nonsense15:68175734-68175734+
TCGA-23-1022-01COSM81581c.477C>Tp.D159DSubstitution - coding silent15:68141953-68141953+
587376COSM1220514c.819A>Tp.E273DSubstitution - Missense15:68146691-68146691+
Pat_30_ACOSM5849633c.191G>Ap.R64QSubstitution - Missense15:68086472-68086472+
8068579COSM3387007c.1052G>Ap.C351YSubstitution - Missense15:68173775-68173775+
SNU-C4COSM4652621c.1041G>Tp.R347RSubstitution - coding silent15:68173764-68173764+
YUQUESTCOSM5383736c.518T>Cp.L173SSubstitution - Missense15:68141994-68141994+
Pat_24_ACOSM4714250c.590A>Gp.Q197RSubstitution - Missense15:68142325-68142325+
ESCC_158COSM5646656c.1277C>Tp.S426FSubstitution - Missense15:68175744-68175744+
35MCOSM4056473c.742C>Tp.R248*Substitution - Nonsense15:68146614-68146614+
T660COSM4714251c.699C>Gp.Y233*Substitution - Nonsense15:68146571-68146571+
TCGA-BR-6452-01COSM4056472c.720C>Tp.G240GSubstitution - coding silent15:68146592-68146592+
PT09_2COSM5895000c.121G>Ap.A41TSubstitution - Missense15:68086402-68086402+
H650COSM1194296c.1130G>Tp.C377FSubstitution - Missense15:68173853-68173853+
TCGA-A2-A25A-01COSM964333c.734G>Tp.R245LSubstitution - Missense15:68146606-68146606+
RKOCOSM4647839c.8A>Gp.D3GSubstitution - Missense15:68054334-68054334+
LC_C9COSM1189051c.394G>Tp.V132FSubstitution - Missense15:68086675-68086675+
YUSCACOSM5383737c.756C>Tp.I252ISubstitution - coding silent15:68146628-68146628+
1_RESISTANTCOSM1719997c.461C>Tp.T154ISubstitution - Missense15:68086742-68086742+
TCGA-56-6545-01COSM701410c.1253C>Tp.S418LSubstitution - Missense15:68175720-68175720+
TCGA-AZ-4315-01COSM1374247c.836C>Tp.S279FSubstitution - Missense15:68153597-68153597+
19COSM5747664c.304C>Tp.H102YSubstitution - Missense15:68086585-68086585+
TCGA-BR-8487-01COSM4056473c.742C>Tp.R248*Substitution - Nonsense15:68146614-68146614+
1N30-VS-1T30COSM4974046c.482G>Ap.S161NSubstitution - Missense15:68141958-68141958+
TCGA-BQ-5876-01COSM3988088c.1782T>Cp.S594SSubstitution - coding silent15:68187661-68187661+
TCGA-AA-3660-01COSM1374246c.314C>Ap.S105*Substitution - Nonsense15:68086595-68086595+
TCGA-D1-A17F-01COSM964335c.1511C>Tp.P504LSubstitution - Missense15:68181241-68181241+
1_PRE-TREATMENTCOSM1719997c.461C>Tp.T154ISubstitution - Missense15:68086742-68086742+
MO_1071COSM5568359c.1353A>Tp.S451SSubstitution - coding silent15:68176526-68176526+
TCGA-C8-A26Y-01COSM3816630c.1057C>Tp.H353YSubstitution - Missense15:68173780-68173780+
TCGA-D3-A3MR-06COSM3503443c.397C>Tp.H133YSubstitution - Missense15:68086678-68086678+
LUAD-D01382COSM391458c.79delGp.R28fs*18Deletion - Frameshift15:68086360-68086360+
TCGA-A4-A5Y1-01COSM3988087c.571A>Gp.K191ESubstitution - Missense15:68142306-68142306+
PD4003aCOSM163469c.1743C>Ap.F581LSubstitution - Missense15:68187622-68187622+
SNUH_G16_S1COSM3999590c.1293A>Gp.G431GSubstitution - coding silent15:68175760-68175760+
TCGA-BR-6706-01COSM4056479c.1729T>Cp.S577PSubstitution - Missense15:68187608-68187608+
TCGA-AM-5820-01COSM5134500c.711delAp.N239fs*47Deletion - Frameshift15:68146583-68146583+
SW620COSM2257804c.1685C>Tp.A562VSubstitution - Missense15:68187564-68187564+
Pat_45_ACOSM5849635c.1075G>Ap.A359TSubstitution - Missense15:68173798-68173798+
TCGA-FW-A3R5-06COSM3887363c.880C>Tp.L294FSubstitution - Missense15:68153641-68153641+
TCGA-B0-5095-01COSM470994c.602G>Ap.R201KSubstitution - Missense15:68142337-68142337+
TCGA-AK-3451-01COSM470995c.867C>Tp.S289SSubstitution - coding silent15:68153628-68153628+
CHEWS001COSM4578443c.666A>Gp.K222KSubstitution - coding silent15:68145879-68145879+
PD4003aCOSM163470c.1557T>Gp.I519MSubstitution - Missense15:68181287-68181287+
HCC143TCOSM5811390c.213G>Tp.T71TSubstitution - coding silent15:68086494-68086494+
TCGA-BR-6452-01COSM4056471c.256C>Ap.P86TSubstitution - Missense15:68086537-68086537+
ESCC_BICR_025TCOSM5434396c.1884C>Gp.T628TSubstitution - coding silent15:68187763-68187763+
TCGA-CG-5721-01COSM4056474c.758C>Tp.T253ISubstitution - Missense15:68146630-68146630+
TCGA-AP-A051-01COSM964328c.213G>Ap.T71TSubstitution - coding silent15:68086494-68086494+
T3610COSM4714250c.590A>Gp.Q197RSubstitution - Missense15:68142325-68142325+
LUAD-RT-S01818COSM383866c.83G>Ap.R28KSubstitution - Missense15:68086364-68086364+
TCGA-D7-A4YV-01COSM4056478c.1074C>Tp.D358DSubstitution - coding silent15:68173797-68173797+
Pat_59_ACOSM4714250c.590A>Gp.Q197RSubstitution - Missense15:68142325-68142325+
TCGA-A3-3380-01COSM1493456c.603-2A>Tp.?Unknown15:68145814-68145814+
TCGA-22-5492-01COSM701411c.596A>Cp.Q199PSubstitution - Missense15:68142331-68142331+
TCGA-D1-A103-01COSM964337c.1625-1G>Ap.?Unknown15:68183629-68183629+
520COSM5612150c.123C>Ap.A41ASubstitution - coding silent15:68086404-68086404+
CSCC-27-TCOSM4476586c.207C>Tp.I69ISubstitution - coding silent15:68086488-68086488+
TCGA-63-5128-01COSM701408c.1687G>Tp.A563SSubstitution - Missense15:68187566-68187566+
TCGA-06-0644COSM2151240c.1330G>Tp.V444LSubstitution - Missense15:68176503-68176503+
PM-2COSM5619530c.1646T>Gp.L549*Substitution - Nonsense15:68183651-68183651+
TCGA-34-5231-01COSM701409c.1263A>Tp.E421DSubstitution - Missense15:68175730-68175730+
TCGA-D1-A16E-01COSM964329c.220G>Ap.D74NSubstitution - Missense15:68086501-68086501+
TCGA-AA-3715-01COSM269884c.1040G>Ap.R347QSubstitution - Missense15:68173763-68173763+
TCGA-AX-A05Z-01COSM964336c.1615G>Ap.D539NSubstitution - Missense15:68181345-68181345+
TCGA-B5-A11O-01COSM964333c.734G>Tp.R245LSubstitution - Missense15:68146606-68146606+
PT37COSM5920866c.1444C>Tp.P482SSubstitution - Missense15:68176617-68176617+
TCGA-BS-A0UF-01COSM964334c.1159A>Gp.I387VSubstitution - Missense15:68173882-68173882+
8058178COSM3387007c.1052G>Ap.C351YSubstitution - Missense15:68173775-68173775+
TCGA-CZ-4859-01COSM470996c.964A>Gp.S322GSubstitution - Missense15:68164760-68164760+
I2L-P7-Tumor-OrganoidCOSM5363099c.210G>Ap.M70ISubstitution - Missense15:68086491-68086491+
TCGA-HU-A4GN-01COSM4056475c.864G>Ap.L288LSubstitution - coding silent15:68153625-68153625+
ESCC_BICR_019TCOSM5431542c.487C>Tp.R163CSubstitution - Missense15:68141963-68141963+
HCC2998COSM2257788c.795G>Ap.T265TSubstitution - coding silent15:68146667-68146667+
CSCC-40-TCOSM194428c.79G>Ap.G27RSubstitution - Missense15:68086360-68086360+
TCGA-BR-8373-01COSM4056477c.893G>Ap.R298QSubstitution - Missense15:68153654-68153654+
Pat_41_BCOSM5849634c.1072G>Ap.D358NSubstitution - Missense15:68173795-68173795+
TCGA-D1-A176-01COSM964331c.479A>Gp.N160SSubstitution - Missense15:68141955-68141955+
260211COSM2257787c.646C>Tp.P216SSubstitution - Missense15:68145859-68145859+
TCGA-B5-A0JY-01COSM964330c.388C>Ap.H130NSubstitution - Missense15:68086669-68086669+
HCC061TCOSM5805855c.1023G>Tp.R341RSubstitution - coding silent15:68173746-68173746+
PT09_1COSM5895000c.121G>Ap.A41TSubstitution - Missense15:68086402-68086402+
TCGA-AA-A01S-01COSM300196c.402G>Ap.P134PSubstitution - coding silent15:68086683-68086683+
SNUH_G10_S1COSM3999590c.1293A>Gp.G431GSubstitution - coding silent15:68175760-68175760+
PDA_006COSM4998133c.1369G>Tp.V457LSubstitution - Missense15:68176542-68176542+
TCGA-46-3768-01COSM701413c.298G>Tp.D100YSubstitution - Missense15:68086579-68086579+
BD141TCOSM5516965c.934+7A>Gp.?Unknown15:68153702-68153702+
98711COSM94965c.1289A>Gp.N430SSubstitution - Missense15:68175756-68175756+
TCGA-AG-3892-01COSM257726c.1471A>Cp.N491HSubstitution - Missense15:68176644-68176644+
RK308_C01COSM3744723c.97C>Tp.R33CSubstitution - Missense15:68086378-68086378+
TCGA-EI-6917-01COSM2257775c.98G>Ap.R33HSubstitution - Missense15:68086379-68086379+
TCGA-B5-A11O-01COSM964332c.721G>Tp.V241LSubstitution - Missense15:68146593-68146593+
TCGA-A2-A25A-01COSM964332c.721G>Tp.V241LSubstitution - Missense15:68146593-68146593+
TCGA-EE-A3JA-06COSM3503444c.1480G>Ap.G494SSubstitution - Missense15:68176653-68176653+
GCT28COSM5749653c.1240G>Ap.A414TSubstitution - Missense15:68175707-68175707+
pfg062TCOSM4756895c.1766T>Gp.F589CSubstitution - Missense15:68187645-68187645+
TCGA-BR-8487-01COSM4056476c.890T>Cp.L297SSubstitution - Missense15:68153651-68153651+
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.162411;Hs.162426;Hs.162430;Hs.16245815q603566
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
ACIntronicSNV.c.829-1907A>C1568444021CLL
ACMissensep.I643Lc.1927A>C1568480144MM
ACMissensep.Q199Pc.596A>C1568434669LUSC
A-Frameshiftp.K420Rfs*17c.1259delA1568468059STAD
AGMissensep.N160Sc.479A>G1568434293UCEC
AGMissensep.S322Gc.964A>G1568457098RCCC
ATMissensep.E421Dc.1263A>T1568468068LUSC
CAIntronicSNV.c.25-8069C>A1568370575CLL
CAMissensep.F581Lc.1743C>A1568479960BRCA
CAMissensep.P227Tc.679C>A1568438230CM
CCTTMissensep.P320Lc.958_959delinsTT1568457092CM
CTIntronicSNV.c.470-21482C>T1568412802CLL
CTMissensep.H133Yc.397C>T1568379016CM
CTMissensep.P504Lc.1511C>T1568473579UCEC
CTMissensep.S418Lc.1253C>T1568468058LUSC
CTSynonymousp.D159Dc.477C>T1568434291OV
CTSynonymousp.S289Sc.867C>T1568445966RCCC
GAMissensep.D74Nc.220G>A1568378839UCEC
GAMissensep.G494Sc.1480G>A1568468991CM
GAMissensep.R201Kc.602G>A1568434675RCCC
GASynonymousp.P134Pc.402G>A1568379021COREAD
G-Frameshiftp.R28Efs*18c.81delG1568378698LUAD
GGATMissensep.G189Mc.565_566delinsAT1568434638CM
GTMissensep.A26Sc.76G>T1568378695LUAD
GTMissensep.A563Sc.1687G>T1568479904LUSC
GTMissensep.D100Yc.298G>T1568378917LUSC
GTMissensep.R245Lc.734G>T1568438944BRCA
GTMissensep.V241Lc.721G>T1568438931BRCA
GTMissensep.V444Lc.1330G>T1568468841GBM
TAIntronicSNV.c.934+80T>A1568446113CM
TCIntronicSNV.c.469+2705T>C1568381793CLL
TCSynonymousp.H500Hc.1500T>C1568473568CM
TGMissensep.I519Mc.1557T>G1568473625BRCA