GNB5
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA155241671452416714+Missense_MutationSNPCCTTCGA-DK-A3WW-01A-22D-A23M-08TCGA-DK-A3WW-10A-01D-A23K-08g.chr15:52416714C>Tc.1132G>Ac.(1132-1134)Gat>Aatp.D378N
BLCA155241674752416747+Missense_MutationSNPCCTTCGA-DK-A1AC-01A-11D-A13W-08TCGA-DK-A1AC-10A-01D-A13W-08g.chr15:52416747C>Tc.1099G>Ac.(1099-1101)Gaa>Aaap.E367K
BRCA155241671152416711+Missense_MutationSNPCCTTCGA-AR-A5QN-01A-12D-A28B-09TCGA-AR-A5QN-10A-01D-A28E-09g.chr15:52416711C>Tc.1135G>Ac.(1135-1137)Ggg>Aggp.G379R
BRCA155244616852446168+Missense_MutationSNPTTCTCGA-AO-A128-01A-11D-A10M-09TCGA-AO-A128-10A-01D-A10M-09g.chr15:52446168T>Cc.344A>Gc.(343-345)aAa>aGap.K115R
CESC155241667352416673+SilentSNPGGTTCGA-Q1-A73O-01A-11D-A32I-09TCGA-Q1-A73O-10B-01D-A32I-09g.chr15:52416673G>Tc.1173C>Ac.(1171-1173)ctC>ctAp.L391L
CESC155241821152418211+Nonsense_MutationSNPCCATCGA-C5-A7CJ-01A-11D-A32I-09TCGA-C5-A7CJ-10A-01D-A32I-09g.chr15:52418211C>Ac.943G>Tc.(943-945)Gag>Tagp.E315*
CESC155242790852427908+Missense_MutationSNPCCGTCGA-HM-A4S6-01A-11D-A26G-09TCGA-HM-A4S6-10A-01D-A26G-09g.chr15:52427908C>Gc.673G>Cc.(673-675)Gag>Cagp.E225Q
CESC155244625652446256+Missense_MutationSNPGGATCGA-C5-A7CL-01A-11D-A32I-09TCGA-C5-A7CL-10A-01D-A32I-09g.chr15:52446256G>Ac.256C>Tc.(256-258)Cgg>Tggp.R86W
CESC155247203652472036+Nonsense_MutationSNPGGTTCGA-JW-A5VL-01A-11D-A28B-09TCGA-JW-A5VL-10A-01D-A28E-09g.chr15:52472036G>Tc.167C>Ac.(166-168)tCg>tAgp.S56*
COAD155241673852416738+Missense_MutationSNPCCTTCGA-D5-5537-01A-21D-1924-10TCGA-D5-5537-10A-01D-1924-10g.chr15:52416738C>Tc.1108G>Ac.(1108-1110)Gtt>Attp.V370I
COAD155241674152416741+Missense_MutationSNPGGATCGA-AA-3877-01A-01W-0995-10TCGA-AA-3877-10A-01W-0995-10g.chr15:52416741G>Ac.1105C>Tc.(1105-1107)Cgc>Tgcp.R369C
COAD155242562852425628+SilentSNPGGATCGA-AA-3663-01A-01D-1719-10TCGA-AA-3663-11A-01D-1719-10g.chr15:52425628G>Ac.810C>Tc.(808-810)tcC>tcTp.S270S
COAD155242793852427938+Missense_MutationSNPCCTTCGA-AZ-6601-01A-11D-1771-10TCGA-AZ-6601-11A-01D-1771-10g.chr15:52427938C>Tc.643G>Ac.(643-645)Ggc>Agcp.G215S
COAD155244614352446143+SilentSNPCCTTCGA-CM-6171-01A-11D-1650-10TCGA-CM-6171-10A-01D-1650-10g.chr15:52446143C>Tc.369G>Ac.(367-369)tcG>tcAp.S123S
COADREAD155241673852416738+Missense_MutationSNPCCTTCGA-D5-5537-01A-21D-1924-10TCGA-D5-5537-10A-01D-1924-10g.chr15:52416738C>Tc.1108G>Ac.(1108-1110)Gtt>Attp.V370I
COADREAD155241674152416741+Missense_MutationSNPGGATCGA-AA-3877-01A-01W-0995-10TCGA-AA-3877-10A-01W-0995-10g.chr15:52416741G>Ac.1105C>Tc.(1105-1107)Cgc>Tgcp.R369C
COADREAD155242562852425628+SilentSNPGGATCGA-AA-3663-01A-01D-1719-10TCGA-AA-3663-11A-01D-1719-10g.chr15:52425628G>Ac.810C>Tc.(808-810)tcC>tcTp.S270S
COADREAD155242793852427938+Missense_MutationSNPCCTTCGA-AZ-6601-01A-11D-1771-10TCGA-AZ-6601-11A-01D-1771-10g.chr15:52427938C>Tc.643G>Ac.(643-645)Ggc>Agcp.G215S
COADREAD155244614352446143+SilentSNPCCTTCGA-CM-6171-01A-11D-1650-10TCGA-CM-6171-10A-01D-1650-10g.chr15:52446143C>Tc.369G>Ac.(367-369)tcG>tcAp.S123S
DLBC155243339752433397+SilentSNPCCTTCGA-G8-6326-01A-11D-2210-10TCGA-G8-6326-10A-01D-2210-10g.chr15:52433397C>Tc.567G>Ac.(565-567)aaG>aaAp.K189K
DLBC155243339752433397+SilentSNPCCTTCGA-GR-7353-01A-11D-2210-10TCGA-GR-7353-10A-01D-2210-10g.chr15:52433397C>Tc.567G>Ac.(565-567)aaG>aaAp.K189K
DLBC155244626052446260+SilentSNPCCTTCGA-G8-6326-01A-11D-2210-10TCGA-G8-6326-10A-01D-2210-10g.chr15:52446260C>Tc.252G>Ac.(250-252)gcG>gcAp.A84A
DLBC155244626052446260+SilentSNPCCTTCGA-GR-7353-01A-11D-2210-10TCGA-GR-7353-10A-01D-2210-10g.chr15:52446260C>Tc.252G>Ac.(250-252)gcG>gcAp.A84A
ESCA155242559752425597+Missense_MutationSNPCCTTCGA-LN-A9FO-01A-11D-A387-09TCGA-LN-A9FO-10A-01D-A38A-09g.chr15:52425597C>Tc.841G>Ac.(841-843)Gaa>Aaap.E281K
GBMLGG155244627152446271+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr15:52446271G>Ac.241C>Tc.(241-243)Cac>Tacp.H81Y
HNSC155242791452427914+Missense_MutationSNPCCTTCGA-MT-A7BN-01A-12D-A34J-08TCGA-MT-A7BN-10A-01D-A34M-08g.chr15:52427914C>Tc.667G>Ac.(667-669)Gac>Aacp.D223N
HNSC155244625552446255+Missense_MutationSNPCCTTCGA-CR-7368-01A-11D-2129-08TCGA-CR-7368-10A-01D-2129-08g.chr15:52446255C>Tc.257G>Ac.(256-258)cGg>cAgp.R86Q
KIPAN155242564452425644+Missense_MutationSNPAAGTCGA-UZ-A9PX-01A-11D-A42J-10TCGA-UZ-A9PX-10A-01D-A42M-10g.chr15:52425644A>Gc.794T>Cc.(793-795)gTg>gCgp.V265A
KIPAN155243345552433455+Missense_MutationSNPTTGTCGA-BP-4347-01A-01D-1366-10TCGA-BP-4347-11A-01D-1366-10g.chr15:52433455T>Gc.509A>Cc.(508-510)aAg>aCgp.K170T
KIPAN155244623952446239+SilentSNPCCTTCGA-A4-7997-01A-11D-2201-08TCGA-A4-7997-10A-01D-2201-08g.chr15:52446239C>Tc.273G>Ac.(271-273)ggG>ggAp.G91G
KIPAN155247683552476835+SilentSNPTTGTCGA-BP-5191-01A-01D-1429-08TCGA-BP-5191-11A-01D-1429-08g.chr15:52476835T>Gc.39A>Cc.(37-39)tcA>tcCp.S13S
KIRC155243345552433455+Missense_MutationSNPTTGTCGA-BP-4347-01A-01D-1366-10TCGA-BP-4347-11A-01D-1366-10g.chr15:52433455T>Gc.509A>Cc.(508-510)aAg>aCgp.K170T
KIRC155247683552476835+SilentSNPTTGTCGA-BP-5191-01A-01D-1429-08TCGA-BP-5191-11A-01D-1429-08g.chr15:52476835T>Gc.39A>Cc.(37-39)tcA>tcCp.S13S
KIRP155242564452425644+Missense_MutationSNPAAGTCGA-UZ-A9PX-01A-11D-A42J-10TCGA-UZ-A9PX-10A-01D-A42M-10g.chr15:52425644A>Gc.794T>Cc.(793-795)gTg>gCgp.V265A
KIRP155244623952446239+SilentSNPCCTTCGA-A4-7997-01A-11D-2201-08TCGA-A4-7997-10A-01D-2201-08g.chr15:52446239C>Tc.273G>Ac.(271-273)ggG>ggAp.G91G
LGG155244627152446271+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr15:52446271G>Ac.241C>Tc.(241-243)Cac>Tacp.H81Y
LIHC155241671952416719+Missense_MutationSNPGGATCGA-G3-AAV3-01A-11D-A36X-10TCGA-G3-AAV3-10A-01D-A370-10g.chr15:52416719G>Ac.1127C>Tc.(1126-1128)tCc>tTcp.S376F
LIHC155241814752418147+Missense_MutationSNPCCATCGA-BC-A10U-01A-11D-A12Z-10TCGA-BC-A10U-11A-11D-A12Z-10g.chr15:52418147C>Ac.1007G>Tc.(1006-1008)aGt>aTtp.S336I
LIHC155247679152476791+Missense_MutationSNPTTATCGA-DD-A1EE-01A-11D-A12Z-10TCGA-DD-A1EE-10A-01D-A12Z-10g.chr15:52476791T>Ac.83A>Tc.(82-84)aAg>aTgp.K28M
LIHC155247679152476791+Missense_MutationSNPTTATCGA-DD-A1EJ-01A-11D-A152-10TCGA-DD-A1EJ-10A-01D-A152-10g.chr15:52476791T>Ac.83A>Tc.(82-84)aAg>aTgp.K28M
LUAD155241824352418243+Splice_SiteSNPTTCTCGA-05-4389-01A-01D-1265-08TCGA-05-4389-10A-01D-1265-08g.chr15:52418243T>Cc.e11-2
LUAD155242040652420406+Missense_MutationSNPGGATCGA-78-7155-01A-11D-2036-08TCGA-78-7155-10A-01D-2036-08g.chr15:52420406G>Ac.899C>Tc.(898-900)tCa>tTap.S300L
LUAD155243334052433340+Missense_MutationSNPCCTTCGA-95-7948-01A-11D-2184-08TCGA-95-7948-10A-01D-2184-08g.chr15:52433340C>Tc.624G>Ac.(622-624)atG>atAp.M208I
LUAD155244210152442101+Missense_MutationSNPCCATCGA-69-7979-01A-11D-2184-08TCGA-69-7979-10A-01D-2184-08g.chr15:52442101C>Ac.397G>Tc.(397-399)Gat>Tatp.D133Y
LUAD155244625052446250+Missense_MutationSNPCCGTCGA-86-8076-01A-31D-2238-08TCGA-86-8076-10A-01D-2238-08g.chr15:52446250C>Gc.262G>Cc.(262-264)Gag>Cagp.E88Q
LUAD155247202552472025+Nonsense_MutationSNPCCATCGA-55-A490-01A-11D-A24D-08TCGA-55-A490-10A-01D-A24F-08g.chr15:52472025C>Ac.178G>Tc.(178-180)Gag>Tagp.E60*
LUAD155247678352476783+Missense_MutationSNPGGCTCGA-NJ-A4YP-01A-11D-A25L-08TCGA-NJ-A4YP-10A-01D-A25L-08g.chr15:52476783G>Cc.91C>Gc.(91-93)Caa>Gaap.Q31E
LUSC155242040452420404+Missense_MutationSNPCCTTCGA-34-5239-01A-21D-1817-08TCGA-34-5239-10A-01D-1817-08g.chr15:52420404C>Tc.901G>Ac.(901-903)Gat>Aatp.D301N
PAAD155242561852425618+Missense_MutationSNPCCTTCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr15:52425618C>Tc.820G>Ac.(820-822)Gtg>Atgp.V274M
PRAD155243340452433404+Missense_MutationSNPTTCTCGA-EJ-5519-01A-01D-1576-08TCGA-EJ-5519-10A-01D-1577-08g.chr15:52433404T>Cc.560A>Gc.(559-561)aAa>aGap.K187R
SKCM155241667652416676+SilentSNPGGATCGA-D3-A2J7-06A-11D-A196-08TCGA-D3-A2J7-10A-01D-A198-08g.chr15:52416676G>Ac.1170C>Tc.(1168-1170)acC>acTp.T390T
SKCM155241821352418213+Missense_MutationSNPCCTTCGA-EE-A2MJ-06A-11D-A197-08TCGA-EE-A2MJ-10A-01D-A199-08g.chr15:52418213C>Tc.941G>Ac.(940-942)aGg>aAgp.R314K
SKCM155243339552433395+Missense_MutationSNPGGATCGA-EE-A2MR-06A-11D-A196-08TCGA-EE-A2MR-10A-01D-A198-08g.chr15:52433395G>Ac.569C>Tc.(568-570)tCt>tTtp.S190F
SKCM155244624552446245+SilentSNPGGATCGA-EE-A29L-06A-12D-A196-08TCGA-EE-A29L-10A-01D-A198-08g.chr15:52446245G>Ac.267C>Tc.(265-267)gcC>gcTp.A89A
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-US155241671452416714single base substitutionCT3_prime_UTR_variant
BLCA-US155241671452416714single base substitutionCTdownstream_gene_variant
BLCA-US155241671452416714single base substitutionCTexon_variant
BLCA-US155241671452416714single base substitutionCTintron_variant
BLCA-US155241671452416714single base substitutionCTmissense_variantD266N796G>A
BLCA-US155241671452416714single base substitutionCTmissense_variantD336N1006G>A
BLCA-US155241671452416714single base substitutionCTmissense_variantD378N1132G>A
BLCA-US155241674752416747single base substitutionCT3_prime_UTR_variant
BLCA-US155241674752416747single base substitutionCTexon_variant
BLCA-US155241674752416747single base substitutionCTintron_variant
BLCA-US155241674752416747single base substitutionCTmissense_variantE255K763G>A
BLCA-US155241674752416747single base substitutionCTmissense_variantE325K973G>A
BLCA-US155241674752416747single base substitutionCTmissense_variantE367K1099G>A
BRCA-EU155240888652408886single base substitutionACdownstream_gene_variant
BRCA-EU155240891452408914single base substitutionGCdownstream_gene_variant
BRCA-EU155240927852409278single base substitutionGTdownstream_gene_variant
BRCA-EU155241242752412427single base substitutionGAdownstream_gene_variant
BRCA-EU155241556752415567single base substitutionGTdownstream_gene_variant
BRCA-EU155241556752415567single base substitutionGTintron_variant
BRCA-EU155241815352418153single base substitutionGT3_prime_UTR_variant
BRCA-EU155241815352418153single base substitutionGTexon_variant
BRCA-EU155241815352418153single base substitutionGTmissense_variantS222Y665C>A
BRCA-EU155241815352418153single base substitutionGTmissense_variantS292Y875C>A
BRCA-EU155241815352418153single base substitutionGTmissense_variantS334Y1001C>A
BRCA-EU155241966052419660single base substitutionCGintron_variant
BRCA-EU155242089052420890single base substitutionCGexon_variant
BRCA-EU155242089052420890single base substitutionCGintron_variant
BRCA-EU155242089052420890single base substitutionCGsplice_region_variant
BRCA-EU155242089052420890single base substitutionCGupstream_gene_variant
BRCA-EU155242094852420948single base substitutionTCexon_variant
BRCA-EU155242094852420948single base substitutionTCintron_variant
BRCA-EU155242094852420948single base substitutionTCupstream_gene_variant
BRCA-EU155242230952422309single base substitutionGCintron_variant
BRCA-EU155242230952422309single base substitutionGCupstream_gene_variant
BRCA-EU155242237852422378single base substitutionCTintron_variant
BRCA-EU155242237852422378single base substitutionCTupstream_gene_variant
BRCA-EU155242364652423646single base substitutionACdownstream_gene_variant
BRCA-EU155242364652423646single base substitutionACintron_variant
BRCA-EU155242364652423646single base substitutionACupstream_gene_variant
BRCA-EU155242437252424372single base substitutionACdownstream_gene_variant
BRCA-EU155242437252424372single base substitutionACintron_variant
BRCA-EU155242437252424372single base substitutionACupstream_gene_variant
BRCA-EU155242455452424554single base substitutionCGdownstream_gene_variant
BRCA-EU155242455452424554single base substitutionCGintron_variant
BRCA-EU155242455452424554single base substitutionCGupstream_gene_variant
BRCA-EU155242743152427431single base substitutionGAdownstream_gene_variant
BRCA-EU155242743152427431single base substitutionGAintron_variant
BRCA-EU155243204452432044single base substitutionCTdownstream_gene_variant
BRCA-EU155243204452432044single base substitutionCTexon_variant
BRCA-EU155243204452432044single base substitutionCTintron_variant
BRCA-EU155243204452432044single base substitutionCTupstream_gene_variant
BRCA-EU155243445952434459single base substitutionTCdownstream_gene_variant
BRCA-EU155243445952434459single base substitutionTCintron_variant
BRCA-EU155243445952434459single base substitutionTCupstream_gene_variant
BRCA-EU155243507552435075single base substitutionGTdownstream_gene_variant
BRCA-EU155243507552435075single base substitutionGTintron_variant
BRCA-EU155243507552435075single base substitutionGTupstream_gene_variant
BRCA-EU155243619952436199single base substitutionGCdownstream_gene_variant
BRCA-EU155243619952436199single base substitutionGCexon_variant
BRCA-EU155243619952436199single base substitutionGCintron_variant
BRCA-EU155243619952436199single base substitutionGCupstream_gene_variant
BRCA-EU155243933252439332single base substitutionACdownstream_gene_variant
BRCA-EU155243933252439332single base substitutionACintron_variant
BRCA-EU155243933252439332single base substitutionACupstream_gene_variant
BRCA-EU155243936952439369single base substitutionTGdownstream_gene_variant
BRCA-EU155243936952439369single base substitutionTGexon_variant
BRCA-EU155243936952439369single base substitutionTGintron_variant
BRCA-EU155243936952439369single base substitutionTGupstream_gene_variant
BRCA-EU155244074152440741single base substitutionCGdownstream_gene_variant
BRCA-EU155244074152440741single base substitutionCGintron_variant
BRCA-EU155244074152440741single base substitutionCGupstream_gene_variant
BRCA-EU155244192652441926single base substitutionCT3_prime_UTR_variant
BRCA-EU155244192652441926single base substitutionCTintron_variant
BRCA-EU155244239852442398single base substitutionCTintron_variant
BRCA-EU155244307552443075single base substitutionGCintron_variant
BRCA-EU155244442352444423deletion of <=200bpA-intron_variant
BRCA-EU155244651152446511deletion of <=200bpT-intron_variant
BRCA-EU155245111052451110single base substitutionCGintron_variant
BRCA-EU155245299252453017deletion of <=200bpTGCCACACCCAGCCTATCATTTTTAA-intron_variant
BRCA-EU155245365152453651single base substitutionCAintron_variant
BRCA-EU155245421852454218single base substitutionCTintron_variant
BRCA-EU155245447452454474single base substitutionGAintron_variant
BRCA-EU155245539252455392single base substitutionCTintron_variant
BRCA-EU155245796052457960single base substitutionCTintron_variant
BRCA-EU155245800552458005single base substitutionGAintron_variant
BRCA-EU155246080552460805deletion of <=200bpA-intron_variant
BRCA-EU155246194052461940single base substitutionCTintron_variant
BRCA-EU155246207052462070insertion of <=200bp-Aintron_variant
BRCA-EU155246758352467583single base substitutionCTintron_variant
BRCA-EU155246824652468246deletion of <=200bpA-intron_variant
BRCA-EU155246824652468246insertion of <=200bp-Aintron_variant
BRCA-EU155247023952470239single base substitutionACintron_variant
BRCA-EU155247404252474042deletion of <=200bpA-intron_variant
BRCA-EU155247404252474042deletion of <=200bpA-upstream_gene_variant
BRCA-EU155247498352474983single base substitutionTCintron_variant
BRCA-EU155247498352474983single base substitutionTCupstream_gene_variant
BRCA-EU155247690752476909deletion of <=200bpAAG-intron_variant
BRCA-EU155247690752476909deletion of <=200bpAAG-upstream_gene_variant
BRCA-EU155247703052477030single base substitutionCTintron_variant
BRCA-EU155247703052477030single base substitutionCTupstream_gene_variant
BRCA-EU155247764052477640single base substitutionCGintron_variant
BRCA-EU155247804352478043single base substitutionTGintron_variant
BRCA-EU155247902252479022single base substitutionGAintron_variant
BRCA-EU155247911852479118single base substitutionAGintron_variant
BRCA-EU155248004452480044single base substitutionGAintron_variant
BRCA-EU155248016852480168deletion of <=200bpT-intron_variant
BRCA-EU155248028952480289single base substitutionTCintron_variant
BRCA-EU155248377652483776single base substitutionGAupstream_gene_variant
BRCA-EU155248436552484365single base substitutionCTupstream_gene_variant
BRCA-EU155248847452488474single base substitutionGCupstream_gene_variant
BRCA-FR155241021852410218single base substitutionCTdownstream_gene_variant
BRCA-FR155244074152440741single base substitutionCGdownstream_gene_variant
BRCA-FR155244074152440741single base substitutionCGintron_variant
BRCA-FR155244074152440741single base substitutionCGupstream_gene_variant
BRCA-FR155244378752443787single base substitutionTCintron_variant
BRCA-FR155246537552465375single base substitutionGAintron_variant
BRCA-UK155242233252422332single base substitutionGCintron_variant
BRCA-UK155242233252422332single base substitutionGCupstream_gene_variant
BRCA-UK155242535652425356single base substitutionCTdownstream_gene_variant
BRCA-UK155242535652425356single base substitutionCTintron_variant
BRCA-UK155242535652425356single base substitutionCTupstream_gene_variant
BRCA-UK155243619952436199single base substitutionGCdownstream_gene_variant
BRCA-UK155243619952436199single base substitutionGCexon_variant
BRCA-UK155243619952436199single base substitutionGCintron_variant
BRCA-UK155243619952436199single base substitutionGCupstream_gene_variant
BRCA-UK155247164852471648single base substitutionGAintron_variant
BRCA-US155241671152416711single base substitutionCT3_prime_UTR_variant
BRCA-US155241671152416711single base substitutionCTdownstream_gene_variant
BRCA-US155241671152416711single base substitutionCTexon_variant
BRCA-US155241671152416711single base substitutionCTintron_variant
BRCA-US155241671152416711single base substitutionCTmissense_variantG267R799G>A
BRCA-US155241671152416711single base substitutionCTmissense_variantG337R1009G>A
BRCA-US155241671152416711single base substitutionCTmissense_variantG379R1135G>A
BRCA-US155244616852446168single base substitutionTCexon_variant
BRCA-US155244616852446168single base substitutionTCmissense_variantK115R344A>G
BRCA-US155244616852446168single base substitutionTCmissense_variantK73R218A>G
BTCA-JP155242775752427757single base substitutionTGdownstream_gene_variant
BTCA-JP155242775752427757single base substitutionTGintron_variant
BTCA-JP155243979052439790single base substitutionTCdownstream_gene_variant
BTCA-JP155243979052439790single base substitutionTCintron_variant
BTCA-JP155243979052439790single base substitutionTCupstream_gene_variant
BTCA-JP155243979152439791single base substitutionTCdownstream_gene_variant
BTCA-JP155243979152439791single base substitutionTCintron_variant
BTCA-JP155243979152439791single base substitutionTCupstream_gene_variant
BTCA-JP155243979252439792single base substitutionCTdownstream_gene_variant
BTCA-JP155243979252439792single base substitutionCTintron_variant
BTCA-JP155243979252439792single base substitutionCTupstream_gene_variant
BTCA-JP155244609952446099single base substitutionAGintron_variant
CESC-US155241667352416673single base substitutionGT3_prime_UTR_variant
CESC-US155241667352416673single base substitutionGTdownstream_gene_variant
CESC-US155241667352416673single base substitutionGTexon_variant
CESC-US155241667352416673single base substitutionGTintron_variant
CESC-US155241667352416673single base substitutionGTsynonymous_variantL279L837C>A
CESC-US155241667352416673single base substitutionGTsynonymous_variantL349L1047C>A
CESC-US155241667352416673single base substitutionGTsynonymous_variantL391L1173C>A
CESC-US155241821152418211single base substitutionCA3_prime_UTR_variant
CESC-US155241821152418211single base substitutionCAexon_variant
CESC-US155241821152418211single base substitutionCAstop_gainedE203*607G>T
CESC-US155241821152418211single base substitutionCAstop_gainedE273*817G>T
CESC-US155241821152418211single base substitutionCAstop_gainedE315*943G>T
CESC-US155242790852427908single base substitutionCG3_prime_UTR_variant
CESC-US155242790852427908single base substitutionCGexon_variant
CESC-US155242790852427908single base substitutionCGmissense_variantE113Q337G>C
CESC-US155242790852427908single base substitutionCGmissense_variantE183Q547G>C
CESC-US155242790852427908single base substitutionCGmissense_variantE225Q673G>C
CESC-US155244625652446256single base substitutionGAexon_variant
CESC-US155244625652446256single base substitutionGAmissense_variantR44W130C>T
CESC-US155244625652446256single base substitutionGAmissense_variantR86W256C>T
CESC-US155247203652472036single base substitutionGTexon_variant
CESC-US155247203652472036single base substitutionGTstop_gainedS14*41C>A
CESC-US155247203652472036single base substitutionGTstop_gainedS56*167C>A
CLLE-ES155240996852409968single base substitutionGCdownstream_gene_variant
CLLE-ES155242978652429786single base substitutionTCdownstream_gene_variant
CLLE-ES155242978652429786single base substitutionTCexon_variant
CLLE-ES155242978652429786single base substitutionTCintron_variant
CLLE-ES155242978652429786single base substitutionTCupstream_gene_variant
CLLE-ES155245973952459739single base substitutionGAintron_variant
COAD-US155241673852416738single base substitutionCT3_prime_UTR_variant
COAD-US155241673852416738single base substitutionCTexon_variant
COAD-US155241673852416738single base substitutionCTintron_variant
COAD-US155241673852416738single base substitutionCTmissense_variantV258I772G>A
COAD-US155241673852416738single base substitutionCTmissense_variantV328I982G>A
COAD-US155241673852416738single base substitutionCTmissense_variantV370I1108G>A
COAD-US155242562852425628single base substitutionGAdownstream_gene_variant
COAD-US155242562852425628single base substitutionGAexon_variant
COAD-US155242562852425628single base substitutionGAsynonymous_variantS158S474C>T
COAD-US155242562852425628single base substitutionGAsynonymous_variantS228S684C>T
COAD-US155242562852425628single base substitutionGAsynonymous_variantS270S810C>T
COAD-US155242562852425628single base substitutionGAupstream_gene_variant
COAD-US155242793852427938single base substitutionCT3_prime_UTR_variant
COAD-US155242793852427938single base substitutionCTexon_variant
COAD-US155242793852427938single base substitutionCTmissense_variantG103S307G>A
COAD-US155242793852427938single base substitutionCTmissense_variantG173S517G>A
COAD-US155242793852427938single base substitutionCTmissense_variantG215S643G>A
COAD-US155244614352446143single base substitutionCTexon_variant
COAD-US155244614352446143single base substitutionCTsynonymous_variantS123S369G>A
COAD-US155244614352446143single base substitutionCTsynonymous_variantS81S243G>A
COCA-CN155241486752414867single base substitutionAC3_prime_UTR_variant
COCA-CN155241486752414867single base substitutionACdownstream_gene_variant
COCA-CN155241486752414867single base substitutionACexon_variant
COCA-CN155241814852418148single base substitutionTC3_prime_UTR_variant
COCA-CN155241814852418148single base substitutionTCexon_variant
COCA-CN155241814852418148single base substitutionTCmissense_variantS224G670A>G
COCA-CN155241814852418148single base substitutionTCmissense_variantS294G880A>G
COCA-CN155241814852418148single base substitutionTCmissense_variantS336G1006A>G
COCA-CN155242101252421012single base substitutionTCintron_variant
COCA-CN155242101252421012single base substitutionTCupstream_gene_variant
COCA-CN155242104052421040single base substitutionGTintron_variant
COCA-CN155242104052421040single base substitutionGTupstream_gene_variant
COCA-CN155242769552427695single base substitutionCAdownstream_gene_variant
COCA-CN155242769552427695single base substitutionCAintron_variant
COCA-CN155243339552433395single base substitutionGT3_prime_UTR_variant
COCA-CN155243339552433395single base substitutionGTdownstream_gene_variant
COCA-CN155243339552433395single base substitutionGTexon_variant
COCA-CN155243339552433395single base substitutionGTintron_variant
COCA-CN155243339552433395single base substitutionGTmissense_variantS148Y443C>A
COCA-CN155243339552433395single base substitutionGTmissense_variantS190Y569C>A
COCA-CN155243339552433395single base substitutionGTupstream_gene_variant
COCA-CN155243361152433611single base substitutionGTintron_variant
COCA-CN155243361152433611single base substitutionGTupstream_gene_variant
COCA-CN155243979152439791single base substitutionTCdownstream_gene_variant
COCA-CN155243979152439791single base substitutionTCintron_variant
COCA-CN155243979152439791single base substitutionTCupstream_gene_variant
COCA-CN155243979252439792single base substitutionCTdownstream_gene_variant
COCA-CN155243979252439792single base substitutionCTintron_variant
COCA-CN155243979252439792single base substitutionCTupstream_gene_variant
COCA-CN155244602352446023single base substitutionGTintron_variant
COCA-CN155248625052486250single base substitutionGTupstream_gene_variant
EOPC-DE155242841152428411single base substitutionTCdownstream_gene_variant
EOPC-DE155242841152428411single base substitutionTCintron_variant
EOPC-DE155242841152428411single base substitutionTCupstream_gene_variant
EOPC-DE155245426452454264single base substitutionAGintron_variant
ESAD-UK155240864352408643single base substitutionATdownstream_gene_variant
ESAD-UK155240928752409287insertion of <=200bp-ATdownstream_gene_variant
ESAD-UK155241202152412021single base substitutionTCdownstream_gene_variant
ESAD-UK155241780052417800single base substitutionTAexon_variant
ESAD-UK155241780052417800single base substitutionTAintron_variant
ESAD-UK155241808552418085single base substitutionCTexon_variant
ESAD-UK155241808552418085single base substitutionCTintron_variant
ESAD-UK155242104252421042single base substitutionGTintron_variant
ESAD-UK155242104252421042single base substitutionGTupstream_gene_variant
ESAD-UK155242703952427039single base substitutionTCdownstream_gene_variant
ESAD-UK155242703952427039single base substitutionTCintron_variant
ESAD-UK155242836952428369deletion of <=200bpA-intron_variant
ESAD-UK155242836952428369deletion of <=200bpA-upstream_gene_variant
ESAD-UK155243462352434623single base substitutionACdownstream_gene_variant
ESAD-UK155243462352434623single base substitutionACintron_variant
ESAD-UK155243462352434623single base substitutionACupstream_gene_variant
ESAD-UK155243513452435134single base substitutionCTdownstream_gene_variant
ESAD-UK155243513452435134single base substitutionCTintron_variant
ESAD-UK155243513452435134single base substitutionCTupstream_gene_variant
ESAD-UK155243707952437079single base substitutionCTdownstream_gene_variant
ESAD-UK155243707952437079single base substitutionCTintron_variant
ESAD-UK155243707952437079single base substitutionCTupstream_gene_variant
ESAD-UK155243863052438630single base substitutionTAdownstream_gene_variant
ESAD-UK155243863052438630single base substitutionTAintron_variant
ESAD-UK155243863052438630single base substitutionTAupstream_gene_variant
ESAD-UK155244078352440783single base substitutionTCdownstream_gene_variant
ESAD-UK155244078352440783single base substitutionTCintron_variant
ESAD-UK155244078352440783single base substitutionTCupstream_gene_variant
ESAD-UK155244566252445662single base substitutionTGintron_variant
ESAD-UK155244625552446255single base substitutionCTexon_variant
ESAD-UK155244625552446255single base substitutionCTmissense_variantR44Q131G>A
ESAD-UK155244625552446255single base substitutionCTmissense_variantR86Q257G>A
ESAD-UK155244929952449299single base substitutionATintron_variant
ESAD-UK155244962352449623single base substitutionTAintron_variant
ESAD-UK155244967652449676single base substitutionCTintron_variant
ESAD-UK155245107052451070single base substitutionACintron_variant
ESAD-UK155245365252453652single base substitutionGAintron_variant
ESAD-UK155245729152457291single base substitutionACintron_variant
ESAD-UK155245753352457533single base substitutionCTintron_variant
ESAD-UK155246007752460077deletion of <=200bpA-intron_variant
ESAD-UK155246014952460149single base substitutionAGintron_variant
ESAD-UK155246113452461134single base substitutionAGintron_variant
ESAD-UK155246701652467016single base substitutionCTintron_variant
ESAD-UK155246720152467201single base substitutionCTintron_variant
ESAD-UK155246825052468250single base substitutionACintron_variant
ESAD-UK155247250152472501single base substitutionACintron_variant
ESAD-UK155247250152472501single base substitutionACupstream_gene_variant
ESAD-UK155247522952475229single base substitutionACintron_variant
ESAD-UK155247522952475229single base substitutionACupstream_gene_variant
ESAD-UK155247594752475947single base substitutionACintron_variant
ESAD-UK155247594752475947single base substitutionACupstream_gene_variant
ESAD-UK155248087352480875deletion of <=200bpAGT-intron_variant
ESAD-UK155248565852485658single base substitutionGAupstream_gene_variant
ESAD-UK155248582952485830deletion of <=200bpAT-upstream_gene_variant
ESAD-UK155248608152486081single base substitutionCGupstream_gene_variant
KIRC-US155243345552433455single base substitutionTG3_prime_UTR_variant
KIRC-US155243345552433455single base substitutionTGexon_variant
KIRC-US155243345552433455single base substitutionTGintron_variant
KIRC-US155243345552433455single base substitutionTGmissense_variantK128T383A>C
KIRC-US155243345552433455single base substitutionTGmissense_variantK170T509A>C
KIRC-US155243345552433455single base substitutionTGupstream_gene_variant
KIRC-US155247683552476835single base substitutionTGexon_variant
KIRC-US155247683552476835single base substitutionTGsynonymous_variantS13S39A>C
KIRC-US155247683552476835single base substitutionTGupstream_gene_variant
KIRP-US155244623952446239single base substitutionCTexon_variant
KIRP-US155244623952446239single base substitutionCTsynonymous_variantG49G147G>A
KIRP-US155244623952446239single base substitutionCTsynonymous_variantG91G273G>A
LAML-KR155240928952409289single base substitutionATdownstream_gene_variant
LAML-KR155242803352428033single base substitutionCTexon_variant
LAML-KR155242803352428033single base substitutionCTintron_variant
LAML-KR155242803452428034single base substitutionCTexon_variant
LAML-KR155242803452428034single base substitutionCTintron_variant
LAML-KR155248630652486306single base substitutionCTupstream_gene_variant
LICA-FR155245388352453883single base substitutionTCintron_variant
LICA-FR155245391652453916single base substitutionTGintron_variant
LICA-FR155245663252456632single base substitutionGAintron_variant
LICA-FR155248231552482316deletion of <=200bpTT-intron_variant
LICA-FR155248551252485514deletion of <=200bpAAA-upstream_gene_variant
LICA-FR155248725652487256single base substitutionACupstream_gene_variant
LIHC-US155241676752416767single base substitutionAG3_prime_UTR_variant
LIHC-US155241676752416767single base substitutionAGexon_variant
LIHC-US155241676752416767single base substitutionAGintron_variant
LIHC-US155241676752416767single base substitutionAGmissense_variantV248A743T>C
LIHC-US155241676752416767single base substitutionAGmissense_variantV318A953T>C
LIHC-US155241676752416767single base substitutionAGmissense_variantV360A1079T>C
LIHC-US155241814752418147single base substitutionCAexon_variant
LIHC-US155241814752418147single base substitutionCAmissense_variantS224I671G>T
LIHC-US155241814752418147single base substitutionCAmissense_variantS294I881G>T
LIHC-US155241814752418147single base substitutionCAmissense_variantS336I1007G>T
LIHC-US155241814752418147single base substitutionCAsplice_region_variant
LIHC-US155247679152476791single base substitutionTAexon_variant
LIHC-US155247679152476791single base substitutionTAmissense_variantK28M83A>T
LIHC-US155247679152476791single base substitutionTAupstream_gene_variant
LINC-JP155243181552431815single base substitutionGAdownstream_gene_variant
LINC-JP155243181552431815single base substitutionGAintron_variant
LINC-JP155243181552431815single base substitutionGAupstream_gene_variant
LINC-JP155243936952439369single base substitutionTGdownstream_gene_variant
LINC-JP155243936952439369single base substitutionTGexon_variant
LINC-JP155243936952439369single base substitutionTGintron_variant
LINC-JP155243936952439369single base substitutionTGupstream_gene_variant
LINC-JP155244600452446004single base substitutionCTintron_variant
LINC-JP155245042052450420single base substitutionCTintron_variant
LINC-JP155248623652486236single base substitutionGTupstream_gene_variant
LIRI-JP155240892852408928single base substitutionTCdownstream_gene_variant
LIRI-JP155240908652409086single base substitutionCTdownstream_gene_variant
LIRI-JP155240919152409191single base substitutionGAdownstream_gene_variant
LIRI-JP155241372352413723single base substitutionGC3_prime_UTR_variant
LIRI-JP155241372352413723single base substitutionGCdownstream_gene_variant
LIRI-JP155241375452413761deletion of <=200bpATCAATCA-3_prime_UTR_variant
LIRI-JP155241375452413761deletion of <=200bpATCAATCA-downstream_gene_variant
LIRI-JP155241409952414099single base substitutionTC3_prime_UTR_variant
LIRI-JP155241409952414099single base substitutionTCdownstream_gene_variant
LIRI-JP155241409952414099single base substitutionTCexon_variant
LIRI-JP155241811252418112single base substitutionGAexon_variant
LIRI-JP155241811252418112single base substitutionGAintron_variant
LIRI-JP155241933752419337single base substitutionCTintron_variant
LIRI-JP155242105652421056deletion of <=200bpA-intron_variant
LIRI-JP155242105652421056deletion of <=200bpA-upstream_gene_variant
LIRI-JP155242139952421399single base substitutionTGintron_variant
LIRI-JP155242139952421399single base substitutionTGupstream_gene_variant
LIRI-JP155242254752422547single base substitutionCTintron_variant
LIRI-JP155242254752422547single base substitutionCTupstream_gene_variant
LIRI-JP155242282652422826single base substitutionTGintron_variant
LIRI-JP155242282652422826single base substitutionTGupstream_gene_variant
LIRI-JP155242378252423782single base substitutionAGdownstream_gene_variant
LIRI-JP155242378252423782single base substitutionAGintron_variant
LIRI-JP155242378252423782single base substitutionAGupstream_gene_variant
LIRI-JP155242571052425740deletion of <=200bpGTCTATAGACAAGGCACGAGTCCCAGTTATA-downstream_gene_variant
LIRI-JP155242571052425740deletion of <=200bpGTCTATAGACAAGGCACGAGTCCCAGTTATA-intron_variant
LIRI-JP155242571052425740deletion of <=200bpGTCTATAGACAAGGCACGAGTCCCAGTTATA-upstream_gene_variant
LIRI-JP155242740152427401single base substitutionGAdownstream_gene_variant
LIRI-JP155242740152427401single base substitutionGAintron_variant
LIRI-JP155242903152429031single base substitutionCTdownstream_gene_variant
LIRI-JP155242903152429031single base substitutionCTintron_variant
LIRI-JP155242903152429031single base substitutionCTupstream_gene_variant
LIRI-JP155242941152429411single base substitutionTCdownstream_gene_variant
LIRI-JP155242941152429411single base substitutionTCexon_variant
LIRI-JP155242941152429411single base substitutionTCintron_variant
LIRI-JP155242941152429411single base substitutionTCupstream_gene_variant
LIRI-JP155242951852429518single base substitutionCGdownstream_gene_variant
LIRI-JP155242951852429518single base substitutionCGexon_variant
LIRI-JP155242951852429518single base substitutionCGintron_variant
LIRI-JP155242951852429518single base substitutionCGupstream_gene_variant
LIRI-JP155242969252429692single base substitutionGCdownstream_gene_variant
LIRI-JP155242969252429692single base substitutionGCexon_variant
LIRI-JP155242969252429692single base substitutionGCintron_variant
LIRI-JP155242969252429692single base substitutionGCupstream_gene_variant
LIRI-JP155243051152430511single base substitutionCAdownstream_gene_variant
LIRI-JP155243051152430511single base substitutionCAintron_variant
LIRI-JP155243051152430511single base substitutionCAupstream_gene_variant
LIRI-JP155243105752431057single base substitutionTCdownstream_gene_variant
LIRI-JP155243105752431057single base substitutionTCintron_variant
LIRI-JP155243105752431057single base substitutionTCupstream_gene_variant
LIRI-JP155243107952431079single base substitutionTGdownstream_gene_variant
LIRI-JP155243107952431079single base substitutionTGintron_variant
LIRI-JP155243107952431079single base substitutionTGupstream_gene_variant
LIRI-JP155243361952433622deletion of <=200bpTTTC-intron_variant
LIRI-JP155243361952433622deletion of <=200bpTTTC-upstream_gene_variant
LIRI-JP155243550952435509deletion of <=200bpT-downstream_gene_variant
LIRI-JP155243550952435509deletion of <=200bpT-intron_variant
LIRI-JP155243550952435509deletion of <=200bpT-upstream_gene_variant
LIRI-JP155243643652436436single base substitutionCGdownstream_gene_variant
LIRI-JP155243643652436436single base substitutionCGexon_variant
LIRI-JP155243643652436436single base substitutionCGintron_variant
LIRI-JP155243643652436436single base substitutionCGupstream_gene_variant
LIRI-JP155243729052437290single base substitutionGAdownstream_gene_variant
LIRI-JP155243729052437290single base substitutionGAintron_variant
LIRI-JP155243729052437290single base substitutionGAupstream_gene_variant
LIRI-JP155243830352438303single base substitutionGAdownstream_gene_variant
LIRI-JP155243830352438303single base substitutionGAintron_variant
LIRI-JP155243830352438303single base substitutionGAupstream_gene_variant
LIRI-JP155243889452438894single base substitutionTCdownstream_gene_variant
LIRI-JP155243889452438894single base substitutionTCintron_variant
LIRI-JP155243889452438894single base substitutionTCupstream_gene_variant
LIRI-JP155243950852439508single base substitutionTCdownstream_gene_variant
LIRI-JP155243950852439508single base substitutionTCexon_variant
LIRI-JP155243950852439508single base substitutionTCintron_variant
LIRI-JP155243950852439508single base substitutionTCupstream_gene_variant
LIRI-JP155244033552440335deletion of <=200bpT-downstream_gene_variant
LIRI-JP155244033552440335deletion of <=200bpT-intron_variant
LIRI-JP155244033552440335deletion of <=200bpT-upstream_gene_variant
LIRI-JP155244241352442413single base substitutionGAintron_variant
LIRI-JP155244260352442603single base substitutionTAintron_variant
LIRI-JP155244336152443361single base substitutionGAintron_variant
LIRI-JP155245231252452312single base substitutionTCintron_variant
LIRI-JP155245314752453147single base substitutionGCintron_variant
LIRI-JP155245372652453726single base substitutionGTintron_variant
LIRI-JP155245455052454550deletion of <=200bpA-intron_variant
LIRI-JP155245685252456852single base substitutionTCintron_variant
LIRI-JP155245895752458957single base substitutionCTintron_variant
LIRI-JP155246035452460354single base substitutionCTintron_variant
LIRI-JP155246268352462683single base substitutionACintron_variant
LIRI-JP155246435152464351single base substitutionGAintron_variant
LIRI-JP155246497952464979single base substitutionTCintron_variant
LIRI-JP155246609452466094single base substitutionTCintron_variant
LIRI-JP155247171752471717single base substitutionCTintron_variant
LIRI-JP155247241652472416single base substitutionGTintron_variant
LIRI-JP155247241652472416single base substitutionGTupstream_gene_variant
LIRI-JP155247334952473349single base substitutionGAintron_variant
LIRI-JP155247334952473349single base substitutionGAupstream_gene_variant
LIRI-JP155247534052475340single base substitutionGAintron_variant
LIRI-JP155247534052475340single base substitutionGAupstream_gene_variant
LIRI-JP155247911652479116single base substitutionCAintron_variant
LIRI-JP155248081352480813single base substitutionAGintron_variant
LIRI-JP155248428352484283single base substitutionTCupstream_gene_variant
LIRI-JP155248663052486630single base substitutionTCupstream_gene_variant
LIRI-JP155248681852486818single base substitutionAGupstream_gene_variant
LUSC-KR155241090952410909single base substitutionTCdownstream_gene_variant
LUSC-KR155241163452411634single base substitutionTGdownstream_gene_variant
LUSC-KR155241251952412519single base substitutionTCdownstream_gene_variant
LUSC-KR155241802752418027single base substitutionCTexon_variant
LUSC-KR155241802752418027single base substitutionCTintron_variant
LUSC-KR155241808452418084single base substitutionGAexon_variant
LUSC-KR155241808452418084single base substitutionGAintron_variant
LUSC-KR155241826852418268single base substitutionCGintron_variant
LUSC-KR155242841152428411single base substitutionTCdownstream_gene_variant
LUSC-KR155242841152428411single base substitutionTCintron_variant
LUSC-KR155242841152428411single base substitutionTCupstream_gene_variant
LUSC-KR155243887252438872single base substitutionCTdownstream_gene_variant
LUSC-KR155243887252438872single base substitutionCTintron_variant
LUSC-KR155243887252438872single base substitutionCTupstream_gene_variant
LUSC-KR155243938252439382single base substitutionATdownstream_gene_variant
LUSC-KR155243938252439382single base substitutionATexon_variant
LUSC-KR155243938252439382single base substitutionATintron_variant
LUSC-KR155243938252439382single base substitutionATupstream_gene_variant
LUSC-KR155244620052446200single base substitutionGAexon_variant
LUSC-KR155244620052446200single base substitutionGAsynonymous_variantH104H312C>T
LUSC-KR155244620052446200single base substitutionGAsynonymous_variantH62H186C>T
LUSC-KR155245437052454370single base substitutionTCintron_variant
LUSC-KR155246176152461761single base substitutionGAintron_variant
LUSC-KR155246862652468626single base substitutionGAintron_variant
LUSC-KR155247053352470533single base substitutionGAintron_variant
LUSC-KR155247206752472067single base substitutionCAexon_variant
LUSC-KR155247206752472067single base substitutionCAstop_gainedE4*10G>T
LUSC-KR155247206752472067single base substitutionCAstop_gainedE46*136G>T
LUSC-KR155247625652476256single base substitutionTAintron_variant
LUSC-KR155247625652476256single base substitutionTAupstream_gene_variant
LUSC-KR155247668752476687single base substitutionACintron_variant
LUSC-KR155247668752476687single base substitutionACupstream_gene_variant
LUSC-KR155247723152477231single base substitutionATintron_variant
LUSC-KR155248317752483177single base substitutionCAintron_variant
LUSC-KR155248502452485024single base substitutionGTupstream_gene_variant
LUSC-KR155248752352487523single base substitutionTAupstream_gene_variant
LUSC-US155242040452420404single base substitutionCT3_prime_UTR_variant
LUSC-US155242040452420404single base substitutionCTexon_variant
LUSC-US155242040452420404single base substitutionCTmissense_variantD189N565G>A
LUSC-US155242040452420404single base substitutionCTmissense_variantD259N775G>A
LUSC-US155242040452420404single base substitutionCTmissense_variantD301N901G>A
LUSC-US155248620952486209single base substitutionCTupstream_gene_variant
MALY-DE155241248552412485single base substitutionCTdownstream_gene_variant
MALY-DE155241339452413394single base substitutionGA3_prime_UTR_variant
MALY-DE155241339452413394single base substitutionGAdownstream_gene_variant
MALY-DE155243066552430665single base substitutionGTdownstream_gene_variant
MALY-DE155243066552430665single base substitutionGTintron_variant
MALY-DE155243066552430665single base substitutionGTupstream_gene_variant
MALY-DE155243301452433014single base substitutionCTdownstream_gene_variant
MALY-DE155243301452433014single base substitutionCTintron_variant
MALY-DE155243301452433014single base substitutionCTupstream_gene_variant
MALY-DE155243478352434783single base substitutionCTdownstream_gene_variant
MALY-DE155243478352434783single base substitutionCTintron_variant
MALY-DE155243478352434783single base substitutionCTupstream_gene_variant
MALY-DE155243508052435080single base substitutionGAdownstream_gene_variant
MALY-DE155243508052435080single base substitutionGAintron_variant
MALY-DE155243508052435080single base substitutionGAupstream_gene_variant
MALY-DE155243667652436676single base substitutionTAdownstream_gene_variant
MALY-DE155243667652436676single base substitutionTAintron_variant
MALY-DE155243667652436676single base substitutionTAupstream_gene_variant
MALY-DE155244681852446822deletion of <=200bpGGTAC-intron_variant
MALY-DE155244719352447193single base substitutionTCintron_variant
MALY-DE155246114152461141single base substitutionCTintron_variant
MALY-DE155246221052462210single base substitutionAGintron_variant
MALY-DE155246689352466893single base substitutionAGintron_variant
MALY-DE155247612152476121single base substitutionTGintron_variant
MALY-DE155247612152476121single base substitutionTGupstream_gene_variant
MALY-DE155248310752483107single base substitutionAGintron_variant
MELA-AU155240860152408602multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU155240886652408866single base substitutionGAdownstream_gene_variant
MELA-AU155240930152409301single base substitutionTAdownstream_gene_variant
MELA-AU155241010452410104single base substitutionGAdownstream_gene_variant
MELA-AU155241060952410609single base substitutionCTdownstream_gene_variant
MELA-AU155241113752411137single base substitutionGAdownstream_gene_variant
MELA-AU155241187752411877single base substitutionGAdownstream_gene_variant
MELA-AU155241187952411879single base substitutionGAdownstream_gene_variant
MELA-AU155241212152412121single base substitutionGAdownstream_gene_variant
MELA-AU155241213652412136single base substitutionGAdownstream_gene_variant
MELA-AU155241220252412202single base substitutionGAdownstream_gene_variant
MELA-AU155241264952412649single base substitutionGAdownstream_gene_variant
MELA-AU155241266952412669single base substitutionGAdownstream_gene_variant
MELA-AU155241296352412963single base substitutionGAdownstream_gene_variant
MELA-AU155241319452413194single base substitutionGA3_prime_UTR_variant
MELA-AU155241319452413194single base substitutionGAdownstream_gene_variant
MELA-AU155241396052413960single base substitutionCT3_prime_UTR_variant
MELA-AU155241396052413960single base substitutionCTdownstream_gene_variant
MELA-AU155241396052413960single base substitutionCTexon_variant
MELA-AU155241510452415104single base substitutionACdownstream_gene_variant
MELA-AU155241510452415104single base substitutionACintron_variant
MELA-AU155241523952415239single base substitutionCAdownstream_gene_variant
MELA-AU155241523952415239single base substitutionCAintron_variant
MELA-AU155241535952415359single base substitutionCTdownstream_gene_variant
MELA-AU155241535952415359single base substitutionCTintron_variant
MELA-AU155241632552416325single base substitutionGAdownstream_gene_variant
MELA-AU155241632552416325single base substitutionGAintron_variant
MELA-AU155241646552416465single base substitutionGAdownstream_gene_variant
MELA-AU155241646552416465single base substitutionGAintron_variant
MELA-AU155241794152417941single base substitutionCAexon_variant
MELA-AU155241794152417941single base substitutionCAintron_variant
MELA-AU155241855852418558single base substitutionTGintron_variant
MELA-AU155241861552418615single base substitutionGAintron_variant
MELA-AU155242006052420060single base substitutionGAintron_variant
MELA-AU155242029652420296single base substitutionCTintron_variant
MELA-AU155242032952420329single base substitutionCTintron_variant
MELA-AU155242046452420464single base substitutionCAexon_variant
MELA-AU155242046452420464single base substitutionCAintron_variant
MELA-AU155242048752420487single base substitutionGAexon_variant
MELA-AU155242048752420487single base substitutionGAintron_variant
MELA-AU155242048752420487single base substitutionGAupstream_gene_variant
MELA-AU155242086152420861single base substitutionGA3_prime_UTR_variant
MELA-AU155242086152420861single base substitutionGAexon_variant
MELA-AU155242086152420861single base substitutionGAintron_variant
MELA-AU155242086152420861single base substitutionGAupstream_gene_variant
MELA-AU155242093352420933single base substitutionGAexon_variant
MELA-AU155242093352420933single base substitutionGAintron_variant
MELA-AU155242093352420933single base substitutionGAupstream_gene_variant
MELA-AU155242094352420943single base substitutionGAexon_variant
MELA-AU155242094352420943single base substitutionGAintron_variant
MELA-AU155242094352420943single base substitutionGAupstream_gene_variant
MELA-AU155242121652421216single base substitutionGAintron_variant
MELA-AU155242121652421216single base substitutionGAupstream_gene_variant
MELA-AU155242167552421675single base substitutionAGintron_variant
MELA-AU155242167552421675single base substitutionAGupstream_gene_variant
MELA-AU155242183652421836single base substitutionGAintron_variant
MELA-AU155242183652421836single base substitutionGAupstream_gene_variant
MELA-AU155242245052422450single base substitutionGAintron_variant
MELA-AU155242245052422450single base substitutionGAupstream_gene_variant
MELA-AU155242248852422488single base substitutionCTintron_variant
MELA-AU155242248852422488single base substitutionCTupstream_gene_variant
MELA-AU155242275752422757single base substitutionATintron_variant
MELA-AU155242275752422757single base substitutionATupstream_gene_variant
MELA-AU155242295952422959single base substitutionGAdownstream_gene_variant
MELA-AU155242295952422959single base substitutionGAintron_variant
MELA-AU155242295952422959single base substitutionGAupstream_gene_variant
MELA-AU155242299152422991single base substitutionGAdownstream_gene_variant
MELA-AU155242299152422991single base substitutionGAintron_variant
MELA-AU155242299152422991single base substitutionGAupstream_gene_variant
MELA-AU155242308652423086single base substitutionGAdownstream_gene_variant
MELA-AU155242308652423086single base substitutionGAintron_variant
MELA-AU155242308652423086single base substitutionGAupstream_gene_variant
MELA-AU155242426752424267single base substitutionGAdownstream_gene_variant
MELA-AU155242426752424267single base substitutionGAintron_variant
MELA-AU155242426752424267single base substitutionGAupstream_gene_variant
MELA-AU155242470352424703single base substitutionGAdownstream_gene_variant
MELA-AU155242470352424703single base substitutionGAintron_variant
MELA-AU155242470352424703single base substitutionGAupstream_gene_variant
MELA-AU155242484952424849single base substitutionTCdownstream_gene_variant
MELA-AU155242484952424849single base substitutionTCintron_variant
MELA-AU155242484952424849single base substitutionTCupstream_gene_variant
MELA-AU155242510052425100single base substitutionACdownstream_gene_variant
MELA-AU155242510052425100single base substitutionACintron_variant
MELA-AU155242510052425100single base substitutionACupstream_gene_variant
MELA-AU155242549852425498single base substitutionGAdownstream_gene_variant
MELA-AU155242549852425498single base substitutionGAintron_variant
MELA-AU155242549852425498single base substitutionGAupstream_gene_variant
MELA-AU155242557452425574single base substitutionCGdownstream_gene_variant
MELA-AU155242557452425574single base substitutionCGsplice_donor_variant
MELA-AU155242557452425574single base substitutionCGupstream_gene_variant
MELA-AU155242586652425866single base substitutionGAdownstream_gene_variant
MELA-AU155242586652425866single base substitutionGAintron_variant
MELA-AU155242586652425866single base substitutionGAupstream_gene_variant
MELA-AU155242595852425958single base substitutionCTdownstream_gene_variant
MELA-AU155242595852425958single base substitutionCTintron_variant
MELA-AU155242595852425958single base substitutionCTupstream_gene_variant
MELA-AU155242606252426062single base substitutionGAdownstream_gene_variant
MELA-AU155242606252426062single base substitutionGAintron_variant
MELA-AU155242660252426602single base substitutionGAdownstream_gene_variant
MELA-AU155242660252426602single base substitutionGAintron_variant
MELA-AU155242766152427661single base substitutionGAdownstream_gene_variant
MELA-AU155242766152427661single base substitutionGAintron_variant
MELA-AU155242797452427974single base substitutionGAexon_variant
MELA-AU155242797452427974single base substitutionGAintron_variant
MELA-AU155242872252428722single base substitutionGAdownstream_gene_variant
MELA-AU155242872252428722single base substitutionGAintron_variant
MELA-AU155242872252428722single base substitutionGAupstream_gene_variant
MELA-AU155242875052428750single base substitutionCAdownstream_gene_variant
MELA-AU155242875052428750single base substitutionCAintron_variant
MELA-AU155242875052428750single base substitutionCAupstream_gene_variant
MELA-AU155242929852429298single base substitutionTGdownstream_gene_variant
MELA-AU155242929852429298single base substitutionTGexon_variant
MELA-AU155242929852429298single base substitutionTGintron_variant
MELA-AU155242929852429298single base substitutionTGupstream_gene_variant
MELA-AU155242982552429825single base substitutionGAdownstream_gene_variant
MELA-AU155242982552429825single base substitutionGAexon_variant
MELA-AU155242982552429825single base substitutionGAintron_variant
MELA-AU155242982552429825single base substitutionGAupstream_gene_variant
MELA-AU155242982552429826multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU155242982552429826multiple base substitution (>=2bp and <=200bp)GGAAexon_variant
MELA-AU155242982552429826multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU155242982552429826multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU155242990252429902single base substitutionGAdownstream_gene_variant
MELA-AU155242990252429902single base substitutionGAexon_variant
MELA-AU155242990252429902single base substitutionGAintron_variant
MELA-AU155242990252429902single base substitutionGAupstream_gene_variant
MELA-AU155243000752430007single base substitutionGAdownstream_gene_variant
MELA-AU155243000752430007single base substitutionGAexon_variant
MELA-AU155243000752430007single base substitutionGAintron_variant
MELA-AU155243000752430007single base substitutionGAupstream_gene_variant
MELA-AU155243026852430268single base substitutionCTdownstream_gene_variant
MELA-AU155243026852430268single base substitutionCTintron_variant
MELA-AU155243026852430268single base substitutionCTupstream_gene_variant
MELA-AU155243038052430380single base substitutionGAdownstream_gene_variant
MELA-AU155243038052430380single base substitutionGAintron_variant
MELA-AU155243038052430380single base substitutionGAupstream_gene_variant
MELA-AU155243098452430984single base substitutionGAdownstream_gene_variant
MELA-AU155243098452430984single base substitutionGAintron_variant
MELA-AU155243098452430984single base substitutionGAupstream_gene_variant
MELA-AU155243156752431567single base substitutionCTdownstream_gene_variant
MELA-AU155243156752431567single base substitutionCTintron_variant
MELA-AU155243156752431567single base substitutionCTupstream_gene_variant
MELA-AU155243174552431745single base substitutionACdownstream_gene_variant
MELA-AU155243174552431745single base substitutionACintron_variant
MELA-AU155243174552431745single base substitutionACupstream_gene_variant
MELA-AU155243182552431825single base substitutionAGdownstream_gene_variant
MELA-AU155243182552431825single base substitutionAGintron_variant
MELA-AU155243182552431825single base substitutionAGupstream_gene_variant
MELA-AU155243189352431893single base substitutionCTdownstream_gene_variant
MELA-AU155243189352431893single base substitutionCTintron_variant
MELA-AU155243189352431893single base substitutionCTupstream_gene_variant
MELA-AU155243253252432532single base substitutionGAdownstream_gene_variant
MELA-AU155243253252432532single base substitutionGAintron_variant
MELA-AU155243253252432532single base substitutionGAupstream_gene_variant
MELA-AU155243298152432981single base substitutionCTdownstream_gene_variant
MELA-AU155243298152432981single base substitutionCTintron_variant
MELA-AU155243298152432981single base substitutionCTupstream_gene_variant
MELA-AU155243310352433103single base substitutionGAdownstream_gene_variant
MELA-AU155243310352433103single base substitutionGAintron_variant
MELA-AU155243310352433103single base substitutionGAupstream_gene_variant
MELA-AU155243396752433967single base substitutionCTintron_variant
MELA-AU155243396752433967single base substitutionCTupstream_gene_variant
MELA-AU155243486352434863single base substitutionGTdownstream_gene_variant
MELA-AU155243486352434863single base substitutionGTintron_variant
MELA-AU155243486352434863single base substitutionGTupstream_gene_variant
MELA-AU155243517152435171single base substitutionGAdownstream_gene_variant
MELA-AU155243517152435171single base substitutionGAintron_variant
MELA-AU155243517152435171single base substitutionGAupstream_gene_variant
MELA-AU155243527552435275single base substitutionCTdownstream_gene_variant
MELA-AU155243527552435275single base substitutionCTintron_variant
MELA-AU155243527552435275single base substitutionCTupstream_gene_variant
MELA-AU155243534152435341single base substitutionGAdownstream_gene_variant
MELA-AU155243534152435341single base substitutionGAintron_variant
MELA-AU155243534152435341single base substitutionGAupstream_gene_variant
MELA-AU155243702652437026single base substitutionCTdownstream_gene_variant
MELA-AU155243702652437026single base substitutionCTintron_variant
MELA-AU155243702652437026single base substitutionCTupstream_gene_variant
MELA-AU155243789052437890single base substitutionGAdownstream_gene_variant
MELA-AU155243789052437890single base substitutionGAintron_variant
MELA-AU155243789052437890single base substitutionGAupstream_gene_variant
MELA-AU155243807852438079multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU155243807852438079multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU155243807852438079multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU155243904652439046single base substitutionCGdownstream_gene_variant
MELA-AU155243904652439046single base substitutionCGintron_variant
MELA-AU155243904652439046single base substitutionCGupstream_gene_variant
MELA-AU155243929252439292single base substitutionGAdownstream_gene_variant
MELA-AU155243929252439292single base substitutionGAintron_variant
MELA-AU155243929252439292single base substitutionGAupstream_gene_variant
MELA-AU155243959852439598single base substitutionGAdownstream_gene_variant
MELA-AU155243959852439598single base substitutionGAexon_variant
MELA-AU155243959852439598single base substitutionGAintron_variant
MELA-AU155243959852439598single base substitutionGAupstream_gene_variant
MELA-AU155243991452439914single base substitutionGAdownstream_gene_variant
MELA-AU155243991452439914single base substitutionGAintron_variant
MELA-AU155243991452439914single base substitutionGAupstream_gene_variant
MELA-AU155244000052440000single base substitutionGAdownstream_gene_variant
MELA-AU155244000052440000single base substitutionGAintron_variant
MELA-AU155244000052440000single base substitutionGAupstream_gene_variant
MELA-AU155244004952440049single base substitutionGAdownstream_gene_variant
MELA-AU155244004952440049single base substitutionGAintron_variant
MELA-AU155244004952440049single base substitutionGAupstream_gene_variant
MELA-AU155244127752441277single base substitutionCAdownstream_gene_variant
MELA-AU155244127752441277single base substitutionCAintron_variant
MELA-AU155244127752441277single base substitutionCAupstream_gene_variant
MELA-AU155244146652441466single base substitutionGAdownstream_gene_variant
MELA-AU155244146652441466single base substitutionGAintron_variant
MELA-AU155244146652441466single base substitutionGAupstream_gene_variant
MELA-AU155244209752442097single base substitutionGAexon_variant
MELA-AU155244209752442097single base substitutionGAmissense_variantS134F401C>T
MELA-AU155244209752442097single base substitutionGAmissense_variantS92F275C>T
MELA-AU155244244152442441single base substitutionCTintron_variant
MELA-AU155244344852443448single base substitutionGAintron_variant
MELA-AU155244364452443644single base substitutionCTintron_variant
MELA-AU155244366552443665single base substitutionCTintron_variant
MELA-AU155244409552444095single base substitutionGAintron_variant
MELA-AU155244488052444880single base substitutionTAintron_variant
MELA-AU155244532352445323single base substitutionGAintron_variant
MELA-AU155244606152446061single base substitutionGAintron_variant
MELA-AU155244624552446245single base substitutionGAexon_variant
MELA-AU155244624552446245single base substitutionGAsynonymous_variantA47A141C>T
MELA-AU155244624552446245single base substitutionGAsynonymous_variantA89A267C>T
MELA-AU155244659552446595single base substitutionCTintron_variant
MELA-AU155244671152446711single base substitutionTCintron_variant
MELA-AU155244677952446779single base substitutionGAintron_variant
MELA-AU155244741252447412single base substitutionGAintron_variant
MELA-AU155244753652447536single base substitutionGAintron_variant
MELA-AU155244882252448822single base substitutionGAintron_variant
MELA-AU155244887252448873multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU155244990152449901single base substitutionGAintron_variant
MELA-AU155245014952450149single base substitutionGAintron_variant
MELA-AU155245019052450191multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU155245025952450259single base substitutionAGintron_variant
MELA-AU155245060252450602single base substitutionGAintron_variant
MELA-AU155245132652451326single base substitutionGAintron_variant
MELA-AU155245148052451481multiple base substitution (>=2bp and <=200bp)GTAAintron_variant
MELA-AU155245152952451529single base substitutionGAintron_variant
MELA-AU155245153852451538single base substitutionGAintron_variant
MELA-AU155245177452451774single base substitutionGAintron_variant
MELA-AU155245178552451785single base substitutionACintron_variant
MELA-AU155245194152451941single base substitutionGAintron_variant
MELA-AU155245242252452422single base substitutionGAintron_variant
MELA-AU155245274452452744single base substitutionGAintron_variant
MELA-AU155245331552453315single base substitutionGAintron_variant
MELA-AU155245366652453666single base substitutionCTintron_variant
MELA-AU155245371852453718single base substitutionGAintron_variant
MELA-AU155245389952453899single base substitutionGAintron_variant
MELA-AU155245431952454319single base substitutionGAintron_variant
MELA-AU155245442952454430multiple base substitution (>=2bp and <=200bp)GGACintron_variant
MELA-AU155245492952454929single base substitutionGAintron_variant
MELA-AU155245540852455408single base substitutionCTintron_variant
MELA-AU155245547052455470single base substitutionGAintron_variant
MELA-AU155245552252455522single base substitutionGAintron_variant
MELA-AU155245588452455884single base substitutionGAintron_variant
MELA-AU155245622352456223single base substitutionGAintron_variant
MELA-AU155245657552456576multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU155245661152456611single base substitutionCTintron_variant
MELA-AU155245708852457088single base substitutionATintron_variant
MELA-AU155245739152457391single base substitutionCTintron_variant
MELA-AU155245774252457742single base substitutionCTintron_variant
MELA-AU155245774952457749single base substitutionCAintron_variant
MELA-AU155245791352457913single base substitutionGAintron_variant
MELA-AU155245810252458102single base substitutionGAintron_variant
MELA-AU155245818352458183single base substitutionGAintron_variant
MELA-AU155245869652458696single base substitutionGAintron_variant
MELA-AU155245979952459799single base substitutionTCintron_variant
MELA-AU155246050552460505single base substitutionGAintron_variant
MELA-AU155246070552460705single base substitutionGAintron_variant
MELA-AU155246080452460804single base substitutionGAintron_variant
MELA-AU155246113552461136multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU155246144352461443single base substitutionGAintron_variant
MELA-AU155246166152461662multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU155246204952462049single base substitutionGAintron_variant
MELA-AU155246208552462085deletion of <=200bpA-intron_variant
MELA-AU155246215152462151single base substitutionGAintron_variant
MELA-AU155246259152462591single base substitutionGAintron_variant
MELA-AU155246277552462775single base substitutionGAintron_variant
MELA-AU155246309452463094single base substitutionGAintron_variant
MELA-AU155246339352463393single base substitutionTCintron_variant
MELA-AU155246517752465177single base substitutionGAintron_variant
MELA-AU155246581552465815single base substitutionGAintron_variant
MELA-AU155246619852466198single base substitutionGAintron_variant
MELA-AU155246621152466211single base substitutionGAintron_variant
MELA-AU155246674552466745single base substitutionTAintron_variant
MELA-AU155246717452467174single base substitutionGAintron_variant
MELA-AU155246732052467320single base substitutionGAintron_variant
MELA-AU155246791552467915single base substitutionGAintron_variant
MELA-AU155246802452468024single base substitutionGAintron_variant
MELA-AU155246888252468882single base substitutionGCintron_variant
MELA-AU155246920552469205single base substitutionGAintron_variant
MELA-AU155246942152469421single base substitutionGAintron_variant
MELA-AU155246942352469423single base substitutionGAintron_variant
MELA-AU155246983552469835single base substitutionGAintron_variant
MELA-AU155247007752470077single base substitutionGAintron_variant
MELA-AU155247041552470415single base substitutionACintron_variant
MELA-AU155247158052471581multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU155247206452472064single base substitutionCTexon_variant
MELA-AU155247206452472064single base substitutionCTmissense_variantG47R139G>A
MELA-AU155247206452472064single base substitutionCTmissense_variantG5R13G>A
MELA-AU155247229052472290single base substitutionCTintron_variant
MELA-AU155247229052472290single base substitutionCTupstream_gene_variant
MELA-AU155247230852472308single base substitutionCTintron_variant
MELA-AU155247230852472308single base substitutionCTupstream_gene_variant
MELA-AU155247359552473595single base substitutionCTintron_variant
MELA-AU155247359552473595single base substitutionCTupstream_gene_variant
MELA-AU155247574652475746single base substitutionGAintron_variant
MELA-AU155247574652475746single base substitutionGAupstream_gene_variant
MELA-AU155247579152475791single base substitutionGAintron_variant
MELA-AU155247579152475791single base substitutionGAupstream_gene_variant
MELA-AU155247579252475792single base substitutionGTintron_variant
MELA-AU155247579252475792single base substitutionGTupstream_gene_variant
MELA-AU155247673652476736single base substitutionAGintron_variant
MELA-AU155247673652476736single base substitutionAGupstream_gene_variant
MELA-AU155247757552477575single base substitutionCTintron_variant
MELA-AU155247760452477604single base substitutionGAintron_variant
MELA-AU155247801252478012single base substitutionGAintron_variant
MELA-AU155247807952478079single base substitutionGAintron_variant
MELA-AU155247808552478085single base substitutionCTintron_variant
MELA-AU155247842252478422single base substitutionCTintron_variant
MELA-AU155247873652478736single base substitutionCTintron_variant
MELA-AU155247873852478738single base substitutionGAintron_variant
MELA-AU155247917452479174single base substitutionCTintron_variant
MELA-AU155247945952479459single base substitutionCTintron_variant
MELA-AU155247958452479584single base substitutionGAintron_variant
MELA-AU155247965852479658single base substitutionGAintron_variant
MELA-AU155247986452479864single base substitutionGTintron_variant
MELA-AU155247993752479937single base substitutionGAintron_variant
MELA-AU155247996752479967single base substitutionGAintron_variant
MELA-AU155248023952480239single base substitutionAGintron_variant
MELA-AU155248038952480389single base substitutionCTintron_variant
MELA-AU155248086652480867multiple base substitution (>=2bp and <=200bp)GCATintron_variant
MELA-AU155248123252481232single base substitutionGAintron_variant
MELA-AU155248137452481374single base substitutionGAintron_variant
MELA-AU155248170552481705single base substitutionGAintron_variant
MELA-AU155248173152481731single base substitutionCTintron_variant
MELA-AU155248280952482809single base substitutionGAintron_variant
MELA-AU155248319652483196single base substitutionCTintron_variant
MELA-AU155248330852483308single base substitutionCTintron_variant
MELA-AU155248401552484015single base substitutionGAupstream_gene_variant
MELA-AU155248404752484047single base substitutionCTupstream_gene_variant
MELA-AU155248409452484094single base substitutionCTupstream_gene_variant
MELA-AU155248412052484120single base substitutionGAupstream_gene_variant
MELA-AU155248414352484143single base substitutionCTupstream_gene_variant
MELA-AU155248480152484801single base substitutionGAupstream_gene_variant
MELA-AU155248709852487098single base substitutionTCupstream_gene_variant
MELA-AU155248725852487258single base substitutionGAupstream_gene_variant
MELA-AU155248735952487359single base substitutionGAupstream_gene_variant
MELA-AU155248737952487379single base substitutionCAupstream_gene_variant
MELA-AU155248739952487399single base substitutionGAupstream_gene_variant
MELA-AU155248749052487490single base substitutionGAupstream_gene_variant
MELA-AU155248766452487664single base substitutionGAupstream_gene_variant
MELA-AU155248775652487756single base substitutionTCupstream_gene_variant
MELA-AU155248790352487903single base substitutionCTupstream_gene_variant
ORCA-IN155241016952410169single base substitutionCGdownstream_gene_variant
ORCA-IN155246609252466092single base substitutionGCintron_variant
ORCA-IN155247799552477996multiple base substitution (>=2bp and <=200bp)TGATintron_variant
ORCA-IN155248303352483033single base substitutionCGintron_variant
ORCA-IN155248582252485822single base substitutionGAupstream_gene_variant
OV-AU155240942752409427single base substitutionAGdownstream_gene_variant
OV-AU155241066652410666single base substitutionCGdownstream_gene_variant
OV-AU155243332052433320single base substitutionGTdownstream_gene_variant
OV-AU155243332052433320single base substitutionGTintron_variant
OV-AU155243332052433320single base substitutionGTupstream_gene_variant
OV-AU155244928752449287single base substitutionCGintron_variant
OV-AU155246623452466234single base substitutionGCintron_variant
OV-AU155247020952470209single base substitutionGAintron_variant
OV-AU155247032052470320single base substitutionCAintron_variant
OV-AU155247161652471616single base substitutionCAintron_variant
OV-AU155248108252481082single base substitutionTCintron_variant
OV-AU155248177252481772single base substitutionGAintron_variant
OV-AU155248341252483412single base substitutionCTintron_variant
PACA-AU155241605652416056single base substitutionGAdownstream_gene_variant
PACA-AU155241605652416056single base substitutionGAintron_variant
PACA-AU155242056952420569single base substitutionGAexon_variant
PACA-AU155242056952420569single base substitutionGAintron_variant
PACA-AU155242056952420569single base substitutionGAupstream_gene_variant
PACA-AU155242478752424787single base substitutionCTdownstream_gene_variant
PACA-AU155242478752424787single base substitutionCTintron_variant
PACA-AU155242478752424787single base substitutionCTupstream_gene_variant
PACA-AU155242491752424917single base substitutionGAdownstream_gene_variant
PACA-AU155242491752424917single base substitutionGAintron_variant
PACA-AU155242491752424917single base substitutionGAupstream_gene_variant
PACA-AU155242547152425471single base substitutionCTdownstream_gene_variant
PACA-AU155242547152425471single base substitutionCTintron_variant
PACA-AU155242547152425471single base substitutionCTupstream_gene_variant
PACA-AU155242841152428411single base substitutionTCdownstream_gene_variant
PACA-AU155242841152428411single base substitutionTCintron_variant
PACA-AU155242841152428411single base substitutionTCupstream_gene_variant
PACA-AU155243413852434138deletion of <=200bpT-intron_variant
PACA-AU155243413852434138deletion of <=200bpT-upstream_gene_variant
PACA-AU155243426052434260single base substitutionGTintron_variant
PACA-AU155243426052434260single base substitutionGTupstream_gene_variant
PACA-AU155243536552435365single base substitutionAGdownstream_gene_variant
PACA-AU155243536552435365single base substitutionAGintron_variant
PACA-AU155243536552435365single base substitutionAGupstream_gene_variant
PACA-AU155244599752445997single base substitutionCAintron_variant
PACA-AU155244978152449781single base substitutionTCintron_variant
PACA-AU155245206052452060single base substitutionGAintron_variant
PACA-AU155245574452455744single base substitutionGCintron_variant
PACA-AU155245844652458446insertion of <=200bp-Tintron_variant
PACA-AU155246085552460855single base substitutionCTintron_variant
PACA-AU155247025652470256single base substitutionCAintron_variant
PACA-AU155247784452477844single base substitutionTGintron_variant
PACA-AU155247877952478779single base substitutionTGintron_variant
PACA-AU155248804952488049single base substitutionGAupstream_gene_variant
PACA-AU155248819552488195single base substitutionATupstream_gene_variant
PACA-AU155248855452488554single base substitutionAGupstream_gene_variant
PACA-CA155240912752409127single base substitutionCTdownstream_gene_variant
PACA-CA155241008052410080single base substitutionCTdownstream_gene_variant
PACA-CA155241196752411967single base substitutionTCdownstream_gene_variant
PACA-CA155241586252415862single base substitutionCTdownstream_gene_variant
PACA-CA155241586252415862single base substitutionCTintron_variant
PACA-CA155241911452419114single base substitutionCGintron_variant
PACA-CA155242466852424668single base substitutionCGdownstream_gene_variant
PACA-CA155242466852424668single base substitutionCGintron_variant
PACA-CA155242466852424668single base substitutionCGupstream_gene_variant
PACA-CA155242841352428413single base substitutionTCdownstream_gene_variant
PACA-CA155242841352428413single base substitutionTCintron_variant
PACA-CA155242841352428413single base substitutionTCupstream_gene_variant
PACA-CA155243237152432371single base substitutionCTdownstream_gene_variant
PACA-CA155243237152432371single base substitutionCTintron_variant
PACA-CA155243237152432371single base substitutionCTupstream_gene_variant
PACA-CA155243552552435525single base substitutionGAdownstream_gene_variant
PACA-CA155243552552435525single base substitutionGAintron_variant
PACA-CA155243552552435525single base substitutionGAupstream_gene_variant
PACA-CA155243771652437716single base substitutionCTdownstream_gene_variant
PACA-CA155243771652437716single base substitutionCTintron_variant
PACA-CA155243771652437716single base substitutionCTupstream_gene_variant
PACA-CA155243979252439792single base substitutionCTdownstream_gene_variant
PACA-CA155243979252439792single base substitutionCTintron_variant
PACA-CA155243979252439792single base substitutionCTupstream_gene_variant
PACA-CA155244822952448229single base substitutionCTintron_variant
PACA-CA155244969152449691single base substitutionTGintron_variant
PACA-CA155245352352453523single base substitutionCGintron_variant
PACA-CA155245933852459338single base substitutionCTintron_variant
PACA-CA155246208952462089single base substitutionATintron_variant
PACA-CA155246958252469582single base substitutionCTintron_variant
PACA-CA155247626852476268single base substitutionCGintron_variant
PACA-CA155247626852476268single base substitutionCGupstream_gene_variant
PACA-CA155248285652482856single base substitutionCTintron_variant
PACA-CA155248472152484721single base substitutionGAupstream_gene_variant
PACA-CA155248535352485353single base substitutionTCupstream_gene_variant
PACA-CA155248584352485843deletion of <=200bpG-upstream_gene_variant
PAEN-AU155241483052414830single base substitutionTC3_prime_UTR_variant
PAEN-AU155241483052414830single base substitutionTCdownstream_gene_variant
PAEN-AU155241483052414830single base substitutionTCexon_variant
PAEN-AU155246027652460276single base substitutionCAintron_variant
PAEN-AU155247973652479736single base substitutionACintron_variant
PAEN-IT155240983152409831single base substitutionGCdownstream_gene_variant
PAEN-IT155241187452411874single base substitutionACdownstream_gene_variant
PAEN-IT155242399352423993single base substitutionTCdownstream_gene_variant
PAEN-IT155242399352423993single base substitutionTCintron_variant
PAEN-IT155242399352423993single base substitutionTCupstream_gene_variant
PBCA-DE155240911652409116insertion of <=200bp-Tdownstream_gene_variant
PBCA-DE155241562152415621insertion of <=200bp-Adownstream_gene_variant
PBCA-DE155241562152415621insertion of <=200bp-Aintron_variant
PBCA-DE155245021552450215insertion of <=200bp-Tintron_variant
PBCA-DE155245986952459869deletion of <=200bpA-intron_variant
PBCA-DE155246759852467598single base substitutionGTintron_variant
PBCA-DE155247227352472273single base substitutionGCintron_variant
PBCA-DE155247227352472273single base substitutionGCupstream_gene_variant
PBCA-DE155248297652482996deletion of <=200bpAAAAAAAAAAAAAAAAAAAAA-intron_variant
PRAD-CA155240919152409191single base substitutionGAdownstream_gene_variant
PRAD-CA155243456952434569single base substitutionGAdownstream_gene_variant
PRAD-CA155243456952434569single base substitutionGAintron_variant
PRAD-CA155243456952434569single base substitutionGAupstream_gene_variant
PRAD-CA155244958852449588single base substitutionCTintron_variant
PRAD-CA155246517352465173single base substitutionATintron_variant
PRAD-UK155244930052449300deletion of <=200bpT-intron_variant
PRAD-UK155247393152473931single base substitutionACintron_variant
PRAD-UK155247393152473931single base substitutionACupstream_gene_variant
PRAD-UK155248744552487445single base substitutionGTupstream_gene_variant
PRAD-US155243340452433404single base substitutionTC3_prime_UTR_variant
PRAD-US155243340452433404single base substitutionTCexon_variant
PRAD-US155243340452433404single base substitutionTCintron_variant
PRAD-US155243340452433404single base substitutionTCmissense_variantK145R434A>G
PRAD-US155243340452433404single base substitutionTCmissense_variantK187R560A>G
PRAD-US155243340452433404single base substitutionTCupstream_gene_variant
READ-US155242041552420415single base substitutionGA3_prime_UTR_variant
READ-US155242041552420415single base substitutionGAexon_variant
READ-US155242041552420415single base substitutionGAmissense_variantA185V554C>T
READ-US155242041552420415single base substitutionGAmissense_variantA255V764C>T
READ-US155242041552420415single base substitutionGAmissense_variantA297V890C>T
RECA-EU155241027552410275single base substitutionGAdownstream_gene_variant
RECA-EU155241075352410753single base substitutionTCdownstream_gene_variant
RECA-EU155247498852474988single base substitutionTCintron_variant
RECA-EU155247498852474988single base substitutionTCupstream_gene_variant
RECA-EU155248604852486048single base substitutionTGupstream_gene_variant
SKCA-BR155240934352409343single base substitutionGAdownstream_gene_variant
SKCA-BR155241169852411698single base substitutionGAdownstream_gene_variant
SKCA-BR155241312952413129single base substitutionGA3_prime_UTR_variant
SKCA-BR155241312952413129single base substitutionGAdownstream_gene_variant
SKCA-BR155241620252416205deletion of <=200bpCAAA-downstream_gene_variant
SKCA-BR155241620252416205deletion of <=200bpCAAA-intron_variant
SKCA-BR155241644452416444single base substitutionAGdownstream_gene_variant
SKCA-BR155241644452416444single base substitutionAGintron_variant
SKCA-BR155243267452432674single base substitutionCTdownstream_gene_variant
SKCA-BR155243267452432674single base substitutionCTintron_variant
SKCA-BR155243267452432674single base substitutionCTupstream_gene_variant
SKCA-BR155243398652433986single base substitutionCTintron_variant
SKCA-BR155243398652433986single base substitutionCTupstream_gene_variant
SKCA-BR155243559952435599single base substitutionATdownstream_gene_variant
SKCA-BR155243559952435599single base substitutionATintron_variant
SKCA-BR155243559952435599single base substitutionATupstream_gene_variant
SKCA-BR155243611152436111single base substitutionACdownstream_gene_variant
SKCA-BR155243611152436111single base substitutionACexon_variant
SKCA-BR155243611152436111single base substitutionACintron_variant
SKCA-BR155243611152436111single base substitutionACupstream_gene_variant
SKCA-BR155243677752436777single base substitutionGAdownstream_gene_variant
SKCA-BR155243677752436777single base substitutionGAintron_variant
SKCA-BR155243677752436777single base substitutionGAupstream_gene_variant
SKCA-BR155243874652438746single base substitutionCTdownstream_gene_variant
SKCA-BR155243874652438746single base substitutionCTintron_variant
SKCA-BR155243874652438746single base substitutionCTupstream_gene_variant
SKCA-BR155243936852439368single base substitutionTGdownstream_gene_variant
SKCA-BR155243936852439368single base substitutionTGexon_variant
SKCA-BR155243936852439368single base substitutionTGintron_variant
SKCA-BR155243936852439368single base substitutionTGupstream_gene_variant
SKCA-BR155244025752440257insertion of <=200bp-CAAAdownstream_gene_variant
SKCA-BR155244025752440257insertion of <=200bp-CAAAintron_variant
SKCA-BR155244025752440257insertion of <=200bp-CAAAupstream_gene_variant
SKCA-BR155244025752440257insertion of <=200bp-CAAdownstream_gene_variant
SKCA-BR155244025752440257insertion of <=200bp-CAAintron_variant
SKCA-BR155244025752440257insertion of <=200bp-CAAupstream_gene_variant
SKCA-BR155244151752441517single base substitutionAC3_prime_UTR_variant
SKCA-BR155244151752441517single base substitutionACintron_variant
SKCA-BR155244151752441517single base substitutionACupstream_gene_variant
SKCA-BR155244243952442439single base substitutionACintron_variant
SKCA-BR155244287252442872single base substitutionCAintron_variant
SKCA-BR155244349952443499single base substitutionGAintron_variant
SKCA-BR155244477552444775single base substitutionGAintron_variant
SKCA-BR155244509052445090single base substitutionAGintron_variant
SKCA-BR155244942852449428single base substitutionCTintron_variant
SKCA-BR155245224852452248single base substitutionGAintron_variant
SKCA-BR155245558652455586single base substitutionGAintron_variant
SKCA-BR155245633052456330single base substitutionTCintron_variant
SKCA-BR155245650552456505insertion of <=200bp-TTAAintron_variant
SKCA-BR155245667452456674single base substitutionTAintron_variant
SKCA-BR155245787452457874single base substitutionCTintron_variant
SKCA-BR155245821052458210single base substitutionGAintron_variant
SKCA-BR155246456952464569single base substitutionCTintron_variant
SKCA-BR155246551552465515single base substitutionACintron_variant
SKCA-BR155246824552468245insertion of <=200bp-CAintron_variant
SKCA-BR155246984752469848deletion of <=200bpCA-intron_variant
SKCA-BR155247007852470078single base substitutionGTintron_variant
SKCA-BR155247173652471736single base substitutionTGintron_variant
SKCA-BR155247190252471902single base substitutionTCintron_variant
SKCA-BR155247586752475867single base substitutionGAintron_variant
SKCA-BR155247586752475867single base substitutionGAupstream_gene_variant
SKCA-BR155247750652477506single base substitutionCTintron_variant
SKCA-BR155247792552477925single base substitutionCTintron_variant
SKCA-BR155247829752478297single base substitutionCTintron_variant
SKCA-BR155248016252480162insertion of <=200bp-TAintron_variant
SKCA-BR155248231552482315single base substitutionTAintron_variant
SKCA-BR155248551152485512deletion of <=200bpCA-upstream_gene_variant
SKCM-US155241667652416676single base substitutionGA3_prime_UTR_variant
SKCM-US155241667652416676single base substitutionGAdownstream_gene_variant
SKCM-US155241667652416676single base substitutionGAexon_variant
SKCM-US155241667652416676single base substitutionGAintron_variant
SKCM-US155241667652416676single base substitutionGAsynonymous_variantT278T834C>T
SKCM-US155241667652416676single base substitutionGAsynonymous_variantT348T1044C>T
SKCM-US155241667652416676single base substitutionGAsynonymous_variantT390T1170C>T
SKCM-US155241674952416749single base substitutionTG3_prime_UTR_variant
SKCM-US155241674952416749single base substitutionTGexon_variant
SKCM-US155241674952416749single base substitutionTGintron_variant
SKCM-US155241674952416749single base substitutionTGmissense_variantH254P761A>C
SKCM-US155241674952416749single base substitutionTGmissense_variantH324P971A>C
SKCM-US155241674952416749single base substitutionTGmissense_variantH366P1097A>C
SKCM-US155241821352418213single base substitutionCT3_prime_UTR_variant
SKCM-US155241821352418213single base substitutionCTexon_variant
SKCM-US155241821352418213single base substitutionCTmissense_variantR202K605G>A
SKCM-US155241821352418213single base substitutionCTmissense_variantR272K815G>A
SKCM-US155241821352418213single base substitutionCTmissense_variantR314K941G>A
SKCM-US155243339552433395single base substitutionGA3_prime_UTR_variant
SKCM-US155243339552433395single base substitutionGAdownstream_gene_variant
SKCM-US155243339552433395single base substitutionGAexon_variant
SKCM-US155243339552433395single base substitutionGAintron_variant
SKCM-US155243339552433395single base substitutionGAmissense_variantS148F443C>T
SKCM-US155243339552433395single base substitutionGAmissense_variantS190F569C>T
SKCM-US155243339552433395single base substitutionGAupstream_gene_variant
SKCM-US155243967752439677single base substitutionGAdownstream_gene_variant
SKCM-US155243967752439677single base substitutionGAexon_variant
SKCM-US155243967752439677single base substitutionGAintron_variant
SKCM-US155243967752439677single base substitutionGAmissense_variantS116L347C>T
SKCM-US155243967752439677single base substitutionGAmissense_variantS158L473C>T
SKCM-US155243967752439677single base substitutionGAupstream_gene_variant
SKCM-US155244624552446245single base substitutionGAexon_variant
SKCM-US155244624552446245single base substitutionGAsynonymous_variantA47A141C>T
SKCM-US155244624552446245single base substitutionGAsynonymous_variantA89A267C>T
SKCM-US155248617952486179single base substitutionGAupstream_gene_variant
SKCM-US155248758552487585single base substitutionGAupstream_gene_variant
STAD-US155241673852416738single base substitutionCT3_prime_UTR_variant
STAD-US155241673852416738single base substitutionCTexon_variant
STAD-US155241673852416738single base substitutionCTintron_variant
STAD-US155241673852416738single base substitutionCTmissense_variantV258I772G>A
STAD-US155241673852416738single base substitutionCTmissense_variantV328I982G>A
STAD-US155241673852416738single base substitutionCTmissense_variantV370I1108G>A
STAD-US155248763952487639single base substitutionTCupstream_gene_variant
THCA-US155248612452486124single base substitutionTCupstream_gene_variant
UCEC-US155242039552420395single base substitutionTCmissense_variantT192A574A>G
UCEC-US155242039552420395single base substitutionTCmissense_variantT262A784A>G
UCEC-US155242039552420395single base substitutionTCmissense_variantT304A910A>G
UCEC-US155242039552420395single base substitutionTCsplice_region_variant
UCEC-US155243969652439696single base substitutionCTdownstream_gene_variant
UCEC-US155243969652439696single base substitutionCTexon_variant
UCEC-US155243969652439696single base substitutionCTintron_variant
UCEC-US155243969652439696single base substitutionCTmissense_variantA110T328G>A
UCEC-US155243969652439696single base substitutionCTmissense_variantA152T454G>A
UCEC-US155243969652439696single base substitutionCTupstream_gene_variant
UCEC-US155244625552446255single base substitutionCTexon_variant
UCEC-US155244625552446255single base substitutionCTmissense_variantR44Q131G>A
UCEC-US155244625552446255single base substitutionCTmissense_variantR86Q257G>A
UCEC-US155248610852486108single base substitutionAGupstream_gene_variant
UCEC-US155248611652486116single base substitutionACupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-DK-A1AC-01COSM1301224c.1099G>Ap.E367KSubstitution - Missense15:52124550-52124550-
T2197COSM4687447c.353G>Tp.R118MSubstitution - Missense15:52153962-52153962-
HDC87COSM4636929c.959C>Tp.S320FSubstitution - Missense15:52125998-52125998-
YURIFCOSM1708186c.401C>Tp.S134FSubstitution - Missense15:52149900-52149900-
YUPAERCOSM5383490c.1013G>Ap.R338HSubstitution - Missense15:52124636-52124636-
TCGA-34-5239-01COSM701037c.901G>Ap.D301NSubstitution - Missense15:52128207-52128207-
HCC2998COSM1373477c.1108G>Ap.V370ISubstitution - Missense15:52124541-52124541-
TCGA-C5-A7CL-01COSM4837832c.256C>Tp.R86WSubstitution - Missense15:52154059-52154059-
HCA7COSM4630120c.1032C>Tp.Y344YSubstitution - coding silent15:52124617-52124617-
sysucc-1397TCOSM5473635c.1006A>Gp.S336GSubstitution - Missense15:52125951-52125951-
SNU-C2BCOSM2217268c.1050C>Tp.N350NSubstitution - coding silent15:52124599-52124599-
S0087COSM5882583c.19C>Tp.L7FSubstitution - Missense15:52184658-52184658-
ATL090COSM5705905c.878G>Ap.G293ESubstitution - Missense15:52128230-52128230-
ccRCC-3COSM1662012c.1162G>Tp.D388YSubstitution - Missense15:52124487-52124487-
TCGA-D3-A2J7-06COSM3502131c.1170C>Tp.T390TSubstitution - coding silent15:52124479-52124479-
TCGA-AX-A0J1-01COSM962795c.454G>Ap.A152TSubstitution - Missense15:52147499-52147499-
SK-MEL-2COSM1678468c.368C>Tp.S123LSubstitution - Missense15:52153947-52153947-
TCGA-AO-A128-01COSM3816323c.344A>Gp.K115RSubstitution - Missense15:52153971-52153971-
ESCC_103COSM5638144c.69G>Ap.L23LSubstitution - coding silent15:52184608-52184608-
TCGA-A5-A0GB-01COSM962794c.910A>Gp.T304ASubstitution - Missense15:52128198-52128198-
TCGA-B8-5551-01COSM470802c.28G>Ap.V10ISubstitution - Missense15:52184649-52184649-
TCGA-AZ-6601-01COSM1373479c.643G>Ap.G215SSubstitution - Missense15:52135741-52135741-
TCGA-BC-A10U-01COSM4942495c.1007G>Tp.S336ISubstitution - Missense15:52125950-52125950-
TCGA-EB-A3XD-01COSM3502135c.473C>Tp.S158LSubstitution - Missense15:52147480-52147480-
TCGA-BP-4347-01COSM3361449c.509A>Cp.K170TSubstitution - Missense15:52141258-52141258-
TCGA-EJ-5519-01COSM1129177c.560A>Gp.K187RSubstitution - Missense15:52141207-52141207-
TCGA-CM-6171-01COSM1373480c.369G>Ap.S123SSubstitution - coding silent15:52153946-52153946-
PD4875aCOSM5785021c.1001C>Ap.S334YSubstitution - Missense15:52125956-52125956-
ESO-189COSM1253366c.906C>Tp.D302DSubstitution - coding silent15:52128202-52128202-
19MCOSM5578634c.1065C>Tp.L355LSubstitution - coding silent15:52124584-52124584-
TCGA-B5-A0JV-01COSM962796c.257G>Ap.R86QSubstitution - Missense15:52154058-52154058-
TARGET-30-PATDWNCOSM1285190c.964G>Tp.E322*Substitution - Nonsense15:52125993-52125993-
C91COSM4444503c.935C>Ap.A312ESubstitution - Missense15:52126022-52126022-
TCGA-F5-6814-01COSM3420417c.890C>Tp.A297VSubstitution - Missense15:52128218-52128218-
PD10059aCOSM3719049c.94C>Tp.Q32*Substitution - Nonsense15:52184583-52184583-
ESO-512COSM1253367c.678C>Tp.S226SSubstitution - coding silent15:52135706-52135706-
TCGA-A3-3365-01COSM1493416c.682C>Ap.Q228KSubstitution - Missense15:52135702-52135702-
NCI-H1395COSM13673c.598G>Tp.A200SSubstitution - Missense15:52141169-52141169-
QC2-33-T2COSM5654554c.265G>Tp.A89SSubstitution - Missense15:52154050-52154050-
TCGA-DK-A3WW-01COSM2217266c.1132G>Ap.D378NSubstitution - Missense15:52124517-52124517-
TCGA-AA-3663-01COSM1373478c.810C>Tp.S270SSubstitution - coding silent15:52133431-52133431-
255COSM3731858c.375+3A>Gp.?Unknown15:52153937-52153937-
TCGA-BP-5191-01COSM470801c.39A>Cp.S13SSubstitution - coding silent15:52184638-52184638-
DLD1COSM2217271c.807C>Tp.R269RSubstitution - coding silent15:52133434-52133434-
TCGA-C5-A7CJ-01COSM4821386c.943G>Tp.E315*Substitution - Nonsense15:52126014-52126014-
sysucc-311TCOSM5478924c.569C>Ap.S190YSubstitution - Missense15:52141198-52141198-
TCGA-EB-A4IS-01COSM3502132c.1097A>Cp.H366PSubstitution - Missense15:52124552-52124552-
TCGA-EE-A2MR-06COSM3502134c.569C>Tp.S190FSubstitution - Missense15:52141198-52141198-
TCGA-G9-6351-01COSM3672071c.627G>Tp.Q209HSubstitution - Missense15:52141140-52141140-
LOVOCOSM2217280c.425C>Tp.A142VSubstitution - Missense15:52147528-52147528-
LAU165COSM234747c.360C>Tp.I120ISubstitution - coding silent15:52153955-52153955-
TCGA-Q1-A73O-01COSM4834550c.1173C>Ap.L391LSubstitution - coding silent15:52124476-52124476-
CHEWS033COSM1373477c.1108G>Ap.V370ISubstitution - Missense15:52124541-52124541-
TCGA-AR-A5QN-01COSM3816322c.1135G>Ap.G379RSubstitution - Missense15:52124514-52124514-
TCGA-D5-5537-01COSM1373477c.1108G>Ap.V370ISubstitution - Missense15:52124541-52124541-
P48COSM328809c.583A>Tp.T195SSubstitution - Missense15:52141184-52141184-
C086COSM962796c.257G>Ap.R86QSubstitution - Missense15:52154058-52154058-
pfg205TCOSM4755254c.1118T>Cp.L373PSubstitution - Missense15:52124531-52124531-
TCGA-HU-A4H8-01COSM1373477c.1108G>Ap.V370ISubstitution - Missense15:52124541-52124541-
188COSM1741553c.832G>Cp.E278QSubstitution - Missense15:52133409-52133409-
C086COSM5531769c.1129C>Tp.P377SSubstitution - Missense15:52124520-52124520-
NPCPR30COSM4995582c.121G>Ap.E41KSubstitution - Missense15:52184556-52184556-
TCGA-HM-A4S6-01COSM4854998c.673G>Cp.E225QSubstitution - Missense15:52135711-52135711-
NPC2FCOSM4995581c.1132G>Tp.D378YSubstitution - Missense15:52124517-52124517-
TCGA-A4-7997-01COSM3988005c.273G>Ap.G91GSubstitution - coding silent15:52154042-52154042-
TCGA-EE-A2MJ-06COSM3502133c.941G>Ap.R314KSubstitution - Missense15:52126016-52126016-
TCGA-EE-A29L-06COSM3502136c.267C>Tp.A89ASubstitution - coding silent15:52154048-52154048-
TCGA-DD-A1EJ-01COSM4934278c.83A>Tp.K28MSubstitution - Missense15:52184594-52184594-
HCT15COSM2217271c.807C>Tp.R269RSubstitution - coding silent15:52133434-52133434-
TCGA-G3-A3CK-01COSM4922502c.1079T>Cp.V360ASubstitution - Missense15:52124570-52124570-
NB2181COSM5703073c.1034A>Gp.N345SSubstitution - Missense15:52124615-52124615-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.15509015q21.2604447
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
ATCAATCA-3-UTRDeletion.c.1185+1198_1185+1205delATTGATAG1552413753HC
CANonsensep.E322*c.964G>T1552418190NB
CTMissensep.D301Nc.901G>A1552420404LUSC
CTMissensep.R314Kc.941G>A1552418213CM
CTMissensep.R86Qc.257G>A1552446255HNSC
CTMissensep.R86Qc.257G>A1552446255UCEC
CTSynonymousp.V131Vc.393G>A1552442105BRCA
GAIntronicSNV.c.1009+33C>T1552418112HC
GAIntronicSNV.c.864-108C>T1552420549CM
GAMissensep.P377Lc.1130C>T1552416716CM
GASynonymousp.A89Ac.267C>T1552446245CM
GASynonymousp.D302Dc.906C>T1552420399ESCA
GASynonymousp.S226Sc.678C>T1552427903ESCA
GASynonymousp.T390Tc.1170C>T1552416676CM
GCMissensep.Q20Ec.58C>G1552476816CM
GCMissensep.R288Gc.862C>G1552425576CM
TCIntronicSNV.c.494+148A>G1552439508HC
TCMissensep.K187Rc.560A>G1552433404PRAD
TCMissensep.T304Ac.910A>G1552420395UCEC
TCSpliceAcceptorSNV.c.913-2A>G1552418243LUAD
TGMissensep.K170Tc.509A>C1552433455RCCC
TGSynonymousp.S13Sc.39A>C1552476835RCCC