PLRG1
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA4155458437155458437+Splice_SiteSNPCCATCGA-ZF-A9RM-01A-11D-A38G-08TCGA-ZF-A9RM-10A-01D-A38J-08g.chr4:155458437C>Ac.e14+1
BLCA4155458505155458505+Missense_MutationSNPGGCTCGA-CF-A1HR-01A-11D-A13W-08TCGA-CF-A1HR-10A-01D-A13W-08g.chr4:155458505G>Cc.1418C>Gc.(1417-1419)tCt>tGtp.S473C
BLCA4155459229155459229+Missense_MutationSNPTTCTCGA-CU-A72E-01A-12D-A339-08TCGA-CU-A72E-10A-01D-A339-08g.chr4:155459229T>Cc.1183A>Gc.(1183-1185)Ata>Gtap.I395V
BLCA4155461192155461192+Missense_MutationSNPCCGTCGA-XF-A9T5-01A-11D-A42E-08TCGA-XF-A9T5-10A-01D-A42H-08g.chr4:155461192C>Gc.953G>Cc.(952-954)aGa>aCap.R318T
BLCA4155470071155470071+Missense_MutationSNPGGCTCGA-4Z-AA7W-01A-11D-A391-08TCGA-4Z-AA7W-10A-01D-A394-08g.chr4:155470071G>Cc.26C>Gc.(25-27)tCt>tGtp.S9C
BRCA4155465643155465643+Missense_MutationSNPGGTTCGA-AN-A0AK-01A-21W-A019-09TCGA-AN-A0AK-10A-01W-A021-09g.chr4:155465643G>Tc.548C>Ac.(547-549)cCt>cAtp.P183H
BRCA4155466998155466998+Missense_MutationSNPGGATCGA-AO-A12E-01A-11D-A10M-09TCGA-AO-A12E-10A-01D-A10M-09g.chr4:155466998G>Ac.482C>Tc.(481-483)gCg>gTgp.A161V
CESC4155461841155461841+Missense_MutationSNPGGATCGA-FU-A3HZ-01A-11D-A20U-09TCGA-FU-A3HZ-10A-01D-A20U-09g.chr4:155461841G>Ac.844C>Tc.(844-846)Cgg>Tggp.R282W
CESC4155470015155470015+Missense_MutationSNPCCTTCGA-JW-A5VJ-01A-11D-A28B-09TCGA-JW-A5VJ-10A-01D-A28E-09g.chr4:155470015C>Tc.82G>Ac.(82-84)Gat>Aatp.D28N
CHOL4155463385155463385+Missense_MutationSNPGGATCGA-W5-AA39-01A-11D-A417-09TCGA-W5-AA39-10A-01D-A41A-09g.chr4:155463385G>Ac.641C>Tc.(640-642)cCt>cTtp.P214L
COAD4155461791155461791+SilentSNPCCTTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr4:155461791C>Tc.894G>Ac.(892-894)ccG>ccAp.P298P
COAD4155465613155465613+Missense_MutationSNPGGATCGA-AA-3947-01A-01W-0995-10TCGA-AA-3947-10A-01W-0995-10g.chr4:155465613G>Ac.578C>Tc.(577-579)cCg>cTgp.P193L
COAD4155465648155465648+Frame_Shift_DelDELTT-TCGA-A6-5665-01A-01D-1650-10TCGA-A6-5665-10A-01D-1650-10g.chr4:155465648delTc.543delAc.(541-543)aaafsp.K181fs
COAD4155468976155468976+Missense_MutationSNPCCTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr4:155468976C>Tc.146G>Ac.(145-147)cGt>cAtp.R49H
COAD4155468977155468977+Missense_MutationSNPGGATCGA-AA-3510-01A-01D-1408-10TCGA-AA-3510-11A-01D-1408-10g.chr4:155468977G>Ac.145C>Tc.(145-147)Cgt>Tgtp.R49C
COADREAD4155457840155457840+Missense_MutationSNPAACTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr4:155457840A>Cc.1542T>Gc.(1540-1542)ttT>ttGp.F514L
COADREAD4155459228155459228+Missense_MutationSNPAAGTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr4:155459228A>Gc.1184T>Cc.(1183-1185)aTa>aCap.I395T
COADREAD4155461791155461791+SilentSNPCCTTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr4:155461791C>Tc.894G>Ac.(892-894)ccG>ccAp.P298P
COADREAD4155461948155461948+Missense_MutationSNPCCTTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr4:155461948C>Tc.826G>Ac.(826-828)Gaa>Aaap.E276K
COADREAD4155465613155465613+Missense_MutationSNPGGATCGA-AA-3947-01A-01W-0995-10TCGA-AA-3947-10A-01W-0995-10g.chr4:155465613G>Ac.578C>Tc.(577-579)cCg>cTgp.P193L
COADREAD4155465648155465648+Frame_Shift_DelDELTT-TCGA-A6-5665-01A-01D-1650-10TCGA-A6-5665-10A-01D-1650-10g.chr4:155465648delTc.543delAc.(541-543)aaafsp.K181fs
COADREAD4155468976155468976+Missense_MutationSNPCCTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr4:155468976C>Tc.146G>Ac.(145-147)cGt>cAtp.R49H
COADREAD4155468977155468977+Missense_MutationSNPGGATCGA-AA-3510-01A-01D-1408-10TCGA-AA-3510-11A-01D-1408-10g.chr4:155468977G>Ac.145C>Tc.(145-147)Cgt>Tgtp.R49C
ESCA4155458497155458497+SilentSNPGGTTCGA-V5-AASW-01A-11D-A403-09TCGA-V5-AASW-10A-01D-A403-09g.chr4:155458497G>Tc.1426C>Ac.(1426-1428)Cga>Agap.R476R
ESCA4155460362155460362+Missense_MutationSNPCCATCGA-IC-A6RE-01A-11D-A33E-09TCGA-IC-A6RE-10A-01D-A33H-09g.chr4:155460362C>Ac.1046G>Tc.(1045-1047)aGc>aTcp.S349I
GBMLGG4155459182155459182+SilentSNPGGATCGA-HT-7680-01A-11D-2253-08TCGA-HT-7680-10A-01D-2253-08g.chr4:155459182G>Ac.1230C>Tc.(1228-1230)tcC>tcTp.S410S
GBMLGG4155463420155463420+SilentSNPCCTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr4:155463420C>Tc.606G>Ac.(604-606)ggG>ggAp.G202G
GBMLGG4155468979155468979+Missense_MutationSNPAACTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr4:155468979A>Cc.143T>Gc.(142-144)cTt>cGtp.L48R
HNSC4155457852155457852+Missense_MutationSNPCCGTCGA-CQ-7071-01A-12D-A30E-08TCGA-CQ-7071-10A-01D-A30H-08g.chr4:155457852C>Gc.1530G>Cc.(1528-1530)aaG>aaCp.K510N
HNSC4155458554155458554+Missense_MutationSNPCCATCGA-CV-A45W-01A-11D-A25D-08TCGA-CV-A45W-10A-01D-A25E-08g.chr4:155458554C>Ac.1369G>Tc.(1369-1371)Ggg>Tggp.G457W
HNSC4155459166155459166+Missense_MutationSNPTTCTCGA-CQ-5332-01A-01D-1683-08TCGA-CQ-5332-10A-01D-1683-08g.chr4:155459166T>Cc.1246A>Gc.(1246-1248)Att>Gttp.I416V
HNSC4155461982155461982+Missense_MutationSNPAACTCGA-CN-A63T-01A-11D-A28R-08TCGA-CN-A63T-10A-01D-A28U-08g.chr4:155461982A>Cc.792T>Gc.(790-792)tgT>tgGp.C264W
KIPAN4155465648155465648+SilentSNPTTCTCGA-A4-7584-01A-11D-2136-08TCGA-A4-7584-10A-01D-2136-08g.chr4:155465648T>Cc.543A>Gc.(541-543)aaA>aaGp.K181K
KIPAN4155470082155470082+SilentSNPTTCTCGA-DZ-6133-01A-11D-1961-08TCGA-DZ-6133-10A-01D-1962-08g.chr4:155470082T>Cc.15A>Gc.(13-15)gtA>gtGp.V5V
KIRP4155465648155465648+SilentSNPTTCTCGA-A4-7584-01A-11D-2136-08TCGA-A4-7584-10A-01D-2136-08g.chr4:155465648T>Cc.543A>Gc.(541-543)aaA>aaGp.K181K
KIRP4155470082155470082+SilentSNPTTCTCGA-DZ-6133-01A-11D-1961-08TCGA-DZ-6133-10A-01D-1962-08g.chr4:155470082T>Cc.15A>Gc.(13-15)gtA>gtGp.V5V
LAML4155458482155458482+Missense_MutationSNPCCTTCGA-AB-2905-03A-01D-0739-09TCGA-AB-2905-11A-01D-0739-09g.chr4:155458482C>Tc.1441G>Ac.(1441-1443)Gaa>Aaap.E481K
LGG4155459182155459182+SilentSNPGGATCGA-HT-7680-01A-11D-2253-08TCGA-HT-7680-10A-01D-2253-08g.chr4:155459182G>Ac.1230C>Tc.(1228-1230)tcC>tcTp.S410S
LGG4155463420155463420+SilentSNPCCTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr4:155463420C>Tc.606G>Ac.(604-606)ggG>ggAp.G202G
LGG4155468979155468979+Missense_MutationSNPAACTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr4:155468979A>Cc.143T>Gc.(142-144)cTt>cGtp.L48R
LIHC4155457860155457860+Missense_MutationSNPTTGTCGA-G3-AAV1-01A-11D-A382-10TCGA-G3-AAV1-10A-01D-A385-10g.chr4:155457860T>Gc.1522A>Cc.(1522-1524)Att>Cttp.I508L
LIHC4155460255155460255+Splice_SiteSNPAAGTCGA-G3-AAV4-01A-11D-A382-10TCGA-G3-AAV4-10A-01D-A385-10g.chr4:155460255A>Gc.e12+1
LIHC4155460301155460301+SilentSNPTTCTCGA-G3-AAV1-01A-11D-A382-10TCGA-G3-AAV1-10A-01D-A385-10g.chr4:155460301T>Cc.1107A>Gc.(1105-1107)acA>acGp.T369T
LIHC4155462030155462030+SilentSNPAAGTCGA-DD-AAD1-01A-11D-A40R-10TCGA-DD-AAD1-10A-01D-A40U-10g.chr4:155462030A>Gc.744T>Cc.(742-744)acT>acCp.T248T
LUAD4155458507155458507+SilentSNPCCTTCGA-75-6214-01A-41D-1945-08TCGA-75-6214-10A-01D-1946-08g.chr4:155458507C>Tc.1416G>Ac.(1414-1416)caG>caAp.Q472Q
LUAD4155459138155459138+Missense_MutationSNPCCATCGA-86-8359-01A-11D-2323-08TCGA-86-8359-10A-01D-2323-08g.chr4:155459138C>Ac.1274G>Tc.(1273-1275)gGa>gTap.G425V
LUAD4155465648155465648+Frame_Shift_DelDELTT-TCGA-55-5899-01A-11D-1625-08TCGA-55-5899-10A-01D-1625-08g.chr4:155465648delTc.543delAc.(541-543)aaafsp.K181fs
LUAD4155468953155468953+Missense_MutationSNPGGTTCGA-05-4396-01A-21D-1855-08TCGA-05-4396-10A-01D-1855-08g.chr4:155468953G>Tc.169C>Ac.(169-171)Cat>Aatp.H57N
LUSC4155458514155458514+Missense_MutationSNPAAGTCGA-18-3415-01A-01D-0983-08TCGA-18-3415-11A-01D-0983-08g.chr4:155458514A>Gc.1409T>Cc.(1408-1410)tTt>tCtp.F470S
LUSC4155459240155459240+Missense_MutationSNPGGCTCGA-46-3769-01A-01D-0983-08TCGA-46-3769-10A-01D-0983-08g.chr4:155459240G>Cc.1172C>Gc.(1171-1173)tCt>tGtp.S391C
LUSC4155460272155460272+Missense_MutationSNPAAGTCGA-18-3409-01A-01D-0983-08TCGA-18-3409-11A-01D-0983-08g.chr4:155460272A>Gc.1136T>Cc.(1135-1137)gTt>gCtp.V379A
LUSC4155461791155461791+SilentSNPCCATCGA-21-1077-01A-01D-1521-08TCGA-21-1077-11A-01D-1521-08g.chr4:155461791C>Ac.894G>Tc.(892-894)ccG>ccTp.P298P
LUSC4155467044155467044+Missense_MutationSNPTTCTCGA-43-6143-01A-11D-1817-08TCGA-43-6143-11A-01D-1817-08g.chr4:155467044T>Cc.436A>Gc.(436-438)Agt>Ggtp.S146G
LUSC4155467273155467273+Splice_SiteSNPAATTCGA-39-5024-01A-21D-1817-08TCGA-39-5024-11A-01D-1817-08g.chr4:155467273A>Tc.e5+1
PAAD4155458483155458483+SilentSNPAACTCGA-HZ-A8P0-01A-11D-A36O-08TCGA-HZ-A8P0-10A-01D-A367-08g.chr4:155458483A>Cc.1440T>Gc.(1438-1440)gcT>gcGp.A480A
PAAD4155465619155465619+Missense_MutationSNPTTCTCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr4:155465619T>Cc.572A>Gc.(571-573)cAc>cGcp.H191R
PRAD4155467028155467028+Missense_MutationSNPGGATCGA-ZG-A9KY-01A-11D-A41K-08TCGA-ZG-A9KY-10A-01D-A41N-08g.chr4:155467028G>Ac.452C>Tc.(451-453)cCt>cTtp.P151L
READ4155457840155457840+Missense_MutationSNPAACTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr4:155457840A>Cc.1542T>Gc.(1540-1542)ttT>ttGp.F514L
READ4155459228155459228+Missense_MutationSNPAAGTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr4:155459228A>Gc.1184T>Cc.(1183-1185)aTa>aCap.I395T
READ4155461948155461948+Missense_MutationSNPCCTTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr4:155461948C>Tc.826G>Ac.(826-828)Gaa>Aaap.E276K
SKCM4155458438155458438+Splice_SiteSNPGGATCGA-FS-A1ZK-06A-11D-A197-08TCGA-FS-A1ZK-10A-01D-A199-08g.chr4:155458438G>Ac.1485C>Tc.(1483-1485)gcC>gcTp.A495A
SKCM4155460287155460287+Missense_MutationSNPGGATCGA-EE-A2MR-06A-11D-A196-08TCGA-EE-A2MR-10A-01D-A198-08g.chr4:155460287G>Ac.1121C>Tc.(1120-1122)tCa>tTap.S374L
SKCM4155461135155461135+Missense_MutationSNPCCTTCGA-D3-A2JK-06A-11D-A196-08TCGA-D3-A2JK-10A-01D-A198-08g.chr4:155461135C>Tc.1010G>Ac.(1009-1011)aGa>aAap.R337K
SKCM4155461949155461949+SilentSNPGGATCGA-FS-A1ZZ-06A-11D-A197-08TCGA-FS-A1ZZ-10A-01D-A199-08g.chr4:155461949G>Ac.825C>Tc.(823-825)ctC>ctTp.L275L
SKCM4155461993155461993+SilentSNPGGATCGA-FS-A1ZQ-06A-11D-A197-08TCGA-FS-A1ZQ-10A-01D-A199-08g.chr4:155461993G>Ac.781C>Tc.(781-783)Ctg>Ttgp.L261L
SKCM4155465644155465644+Missense_MutationSNPGGATCGA-FS-A1ZF-06A-12D-A197-08TCGA-FS-A1ZF-10A-01D-A199-08g.chr4:155465644G>Ac.547C>Tc.(547-549)Cct>Tctp.P183S
SKCM4155467365155467365+Splice_SiteSNPCCTTCGA-EE-A29V-06A-12D-A197-08TCGA-EE-A29V-10A-01D-A199-08g.chr4:155467365C>Tc.314G>Ac.(313-315)gGg>gAgp.G105E
SKCM4155469997155469997+Missense_MutationSNPGGATCGA-FW-A3TU-06A-11D-A23B-08TCGA-FW-A3TU-10A-01D-A23B-08g.chr4:155469997G>Ac.100C>Tc.(100-102)Cct>Tctp.P34S
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
ALL-US4155468900155468900single base substitutionCT3_prime_UTR_variant
ALL-US4155468900155468900single base substitutionCTexon_variant
ALL-US4155468900155468900single base substitutionCTsynonymous_variantT72T216G>A
ALL-US4155468900155468900single base substitutionCTsynonymous_variantT74T222G>A
ALL-US4155468900155468900single base substitutionCTupstream_gene_variant
BLCA-CN4155462069155462069single base substitutionAG3_prime_UTR_variant
BLCA-CN4155462069155462069single base substitutionAGdownstream_gene_variant
BLCA-CN4155462069155462069single base substitutionAGexon_variant
BLCA-CN4155462069155462069single base substitutionAGsynonymous_variantS226S678T>C
BLCA-CN4155462069155462069single base substitutionAGsynonymous_variantS235S705T>C
BLCA-CN4155462069155462069single base substitutionAGupstream_gene_variant
BLCA-US4155458505155458505single base substitutionGC3_prime_UTR_variant
BLCA-US4155458505155458505single base substitutionGCdownstream_gene_variant
BLCA-US4155458505155458505single base substitutionGCexon_variant
BLCA-US4155458505155458505single base substitutionGCintron_variant
BLCA-US4155458505155458505single base substitutionGCmissense_variantS464C1391C>G
BLCA-US4155458505155458505single base substitutionGCmissense_variantS473C1418C>G
BRCA-EU4155455228155455228single base substitutionAGdownstream_gene_variant
BRCA-EU4155456269155456272deletion of <=200bpAACA-3_prime_UTR_variant
BRCA-EU4155456269155456272deletion of <=200bpAACA-downstream_gene_variant
BRCA-EU4155456564155456564single base substitutionAG3_prime_UTR_variant
BRCA-EU4155456564155456564single base substitutionAGdownstream_gene_variant
BRCA-EU4155457474155457474deletion of <=200bpA-3_prime_UTR_variant
BRCA-EU4155457474155457474deletion of <=200bpA-downstream_gene_variant
BRCA-EU4155459333155459333single base substitutionAGdownstream_gene_variant
BRCA-EU4155459333155459333single base substitutionAGintron_variant
BRCA-EU4155459333155459333single base substitutionAGupstream_gene_variant
BRCA-EU4155459555155459555single base substitutionGAdownstream_gene_variant
BRCA-EU4155459555155459555single base substitutionGAintron_variant
BRCA-EU4155459555155459555single base substitutionGAupstream_gene_variant
BRCA-EU4155460391155460391single base substitutionCGdownstream_gene_variant
BRCA-EU4155460391155460391single base substitutionCGintron_variant
BRCA-EU4155460391155460391single base substitutionCGupstream_gene_variant
BRCA-EU4155460398155460398single base substitutionTCdownstream_gene_variant
BRCA-EU4155460398155460398single base substitutionTCintron_variant
BRCA-EU4155460398155460398single base substitutionTCupstream_gene_variant
BRCA-EU4155462231155462231single base substitutionCGdownstream_gene_variant
BRCA-EU4155462231155462231single base substitutionCGintron_variant
BRCA-EU4155462231155462231single base substitutionCGupstream_gene_variant
BRCA-EU4155462941155462941single base substitutionGAdownstream_gene_variant
BRCA-EU4155462941155462941single base substitutionGAintron_variant
BRCA-EU4155462941155462941single base substitutionGAupstream_gene_variant
BRCA-EU4155464832155464832single base substitutionGCdownstream_gene_variant
BRCA-EU4155464832155464832single base substitutionGCintron_variant
BRCA-EU4155464832155464832single base substitutionGCupstream_gene_variant
BRCA-EU4155464932155464932single base substitutionTAdownstream_gene_variant
BRCA-EU4155464932155464932single base substitutionTAintron_variant
BRCA-EU4155464932155464932single base substitutionTAupstream_gene_variant
BRCA-EU4155465294155465294deletion of <=200bpC-downstream_gene_variant
BRCA-EU4155465294155465294deletion of <=200bpC-intron_variant
BRCA-EU4155465294155465294deletion of <=200bpC-upstream_gene_variant
BRCA-EU4155465402155465402single base substitutionGAdownstream_gene_variant
BRCA-EU4155465402155465402single base substitutionGAintron_variant
BRCA-EU4155465402155465402single base substitutionGAupstream_gene_variant
BRCA-EU4155466572155466572single base substitutionTCdownstream_gene_variant
BRCA-EU4155466572155466572single base substitutionTCintron_variant
BRCA-EU4155466572155466572single base substitutionTCupstream_gene_variant
BRCA-EU4155467005155467005single base substitutionGTdownstream_gene_variant
BRCA-EU4155467005155467005single base substitutionGTexon_variant
BRCA-EU4155467005155467005single base substitutionGTmissense_variantP150T448C>A
BRCA-EU4155467005155467005single base substitutionGTmissense_variantP157T469C>A
BRCA-EU4155467005155467005single base substitutionGTmissense_variantP159T475C>A
BRCA-EU4155467005155467005single base substitutionGTupstream_gene_variant
BRCA-EU4155468226155468226single base substitutionCAdownstream_gene_variant
BRCA-EU4155468226155468226single base substitutionCAintron_variant
BRCA-EU4155468226155468226single base substitutionCAupstream_gene_variant
BRCA-EU4155468238155468238single base substitutionCAdownstream_gene_variant
BRCA-EU4155468238155468238single base substitutionCAintron_variant
BRCA-EU4155468238155468238single base substitutionCAupstream_gene_variant
BRCA-EU4155469150155469150single base substitutionCTintron_variant
BRCA-EU4155469150155469150single base substitutionCTupstream_gene_variant
BRCA-EU4155469203155469203single base substitutionCTintron_variant
BRCA-EU4155469203155469203single base substitutionCTupstream_gene_variant
BRCA-EU4155469406155469406single base substitutionCTintron_variant
BRCA-EU4155469406155469406single base substitutionCTupstream_gene_variant
BRCA-EU4155470615155470615deletion of <=200bpA-intron_variant
BRCA-EU4155470615155470615deletion of <=200bpA-upstream_gene_variant
BRCA-EU4155471500155471500single base substitutionCG5_prime_UTR_variant
BRCA-EU4155471500155471500single base substitutionCGexon_variant
BRCA-EU4155471500155471500single base substitutionCGupstream_gene_variant
BRCA-EU4155472055155472055single base substitutionGCupstream_gene_variant
BRCA-EU4155472566155472566single base substitutionGTupstream_gene_variant
BRCA-EU4155472716155472716single base substitutionTCupstream_gene_variant
BRCA-EU4155473979155473979single base substitutionCTupstream_gene_variant
BRCA-EU4155474333155474333single base substitutionATupstream_gene_variant
BRCA-EU4155474504155474504single base substitutionTAupstream_gene_variant
BRCA-EU4155474733155474733single base substitutionGTupstream_gene_variant
BRCA-EU4155475183155475183single base substitutionTGupstream_gene_variant
BRCA-EU4155475668155475668single base substitutionAGupstream_gene_variant
BRCA-EU4155476378155476378single base substitutionTAupstream_gene_variant
BRCA-EU4155476392155476392single base substitutionTAupstream_gene_variant
BRCA-FR4155459555155459555single base substitutionGAdownstream_gene_variant
BRCA-FR4155459555155459555single base substitutionGAintron_variant
BRCA-FR4155459555155459555single base substitutionGAupstream_gene_variant
BRCA-FR4155460391155460391single base substitutionCGdownstream_gene_variant
BRCA-FR4155460391155460391single base substitutionCGintron_variant
BRCA-FR4155460391155460391single base substitutionCGupstream_gene_variant
BRCA-FR4155460398155460398single base substitutionTCdownstream_gene_variant
BRCA-FR4155460398155460398single base substitutionTCintron_variant
BRCA-FR4155460398155460398single base substitutionTCupstream_gene_variant
BRCA-FR4155469406155469406single base substitutionCTintron_variant
BRCA-FR4155469406155469406single base substitutionCTupstream_gene_variant
BRCA-FR4155473383155473383single base substitutionGAupstream_gene_variant
BRCA-UK4155475183155475183single base substitutionTGupstream_gene_variant
BRCA-UK4155475668155475668single base substitutionAGupstream_gene_variant
BRCA-US4155465643155465643single base substitutionGT3_prime_UTR_variant
BRCA-US4155465643155465643single base substitutionGTdownstream_gene_variant
BRCA-US4155465643155465643single base substitutionGTexon_variant
BRCA-US4155465643155465643single base substitutionGTmissense_variantP174H521C>A
BRCA-US4155465643155465643single base substitutionGTmissense_variantP181H542C>A
BRCA-US4155465643155465643single base substitutionGTmissense_variantP183H548C>A
BRCA-US4155465643155465643single base substitutionGTupstream_gene_variant
BRCA-US4155466998155466998single base substitutionGAdownstream_gene_variant
BRCA-US4155466998155466998single base substitutionGAexon_variant
BRCA-US4155466998155466998single base substitutionGAmissense_variantA152V455C>T
BRCA-US4155466998155466998single base substitutionGAmissense_variantA159V476C>T
BRCA-US4155466998155466998single base substitutionGAmissense_variantA161V482C>T
BRCA-US4155466998155466998single base substitutionGAupstream_gene_variant
BTCA-JP4155457904155457904single base substitutionTCdownstream_gene_variant
BTCA-JP4155457904155457904single base substitutionTCintron_variant
BTCA-JP4155470090155470090deletion of <=200bpA-splice_region_variant
BTCA-JP4155470090155470090deletion of <=200bpA-upstream_gene_variant
CESC-US4155461841155461841single base substitutionGA3_prime_UTR_variant
CESC-US4155461841155461841single base substitutionGAdownstream_gene_variant
CESC-US4155461841155461841single base substitutionGAexon_variant
CESC-US4155461841155461841single base substitutionGAmissense_variantR273W817C>T
CESC-US4155461841155461841single base substitutionGAmissense_variantR282W844C>T
CESC-US4155461841155461841single base substitutionGAupstream_gene_variant
CESC-US4155470015155470015single base substitutionCT3_prime_UTR_variant
CESC-US4155470015155470015single base substitutionCTexon_variant
CESC-US4155470015155470015single base substitutionCTmissense_variantD26N76G>A
CESC-US4155470015155470015single base substitutionCTmissense_variantD28N82G>A
CESC-US4155470015155470015single base substitutionCTupstream_gene_variant
CLLE-ES4155474996155474996single base substitutionTCupstream_gene_variant
COAD-US4155459194155459194single base substitutionAT3_prime_UTR_variant
COAD-US4155459194155459194single base substitutionATdownstream_gene_variant
COAD-US4155459194155459194single base substitutionATsynonymous_variantI397I1191T>A
COAD-US4155459194155459194single base substitutionATsynonymous_variantI406I1218T>A
COAD-US4155459194155459194single base substitutionATsynonymous_variantI49I147T>A
COAD-US4155459194155459194single base substitutionATupstream_gene_variant
COAD-US4155461113155461113single base substitutionTCdownstream_gene_variant
COAD-US4155461113155461113single base substitutionTCexon_variant
COAD-US4155461113155461113single base substitutionTCsynonymous_variantQ335Q1005A>G
COAD-US4155461113155461113single base substitutionTCsynonymous_variantQ344Q1032A>G
COAD-US4155461113155461113single base substitutionTCupstream_gene_variant
COAD-US4155461791155461791single base substitutionCTdownstream_gene_variant
COAD-US4155461791155461791single base substitutionCTexon_variant
COAD-US4155461791155461791single base substitutionCTsynonymous_variantP289P867G>A
COAD-US4155461791155461791single base substitutionCTsynonymous_variantP298P894G>A
COAD-US4155461791155461791single base substitutionCTupstream_gene_variant
COAD-US4155468977155468977single base substitutionGA3_prime_UTR_variant
COAD-US4155468977155468977single base substitutionGAexon_variant
COAD-US4155468977155468977single base substitutionGAmissense_variantR47C139C>T
COAD-US4155468977155468977single base substitutionGAmissense_variantR49C145C>T
COAD-US4155468977155468977single base substitutionGAupstream_gene_variant
COAD-US4155470090155470090deletion of <=200bpA-splice_region_variant
COAD-US4155470090155470090deletion of <=200bpA-upstream_gene_variant
COCA-CN4155458497155458497single base substitutionGA3_prime_UTR_variant
COCA-CN4155458497155458497single base substitutionGAdownstream_gene_variant
COCA-CN4155458497155458497single base substitutionGAexon_variant
COCA-CN4155458497155458497single base substitutionGAintron_variant
COCA-CN4155458497155458497single base substitutionGAstop_gainedR467*1399C>T
COCA-CN4155458497155458497single base substitutionGAstop_gainedR476*1426C>T
COCA-CN4155462026155462026single base substitutionGA3_prime_UTR_variant
COCA-CN4155462026155462026single base substitutionGAdownstream_gene_variant
COCA-CN4155462026155462026single base substitutionGAexon_variant
COCA-CN4155462026155462026single base substitutionGAmissense_variantR241W721C>T
COCA-CN4155462026155462026single base substitutionGAmissense_variantR250W748C>T
COCA-CN4155462026155462026single base substitutionGAupstream_gene_variant
COCA-CN4155462188155462188single base substitutionACdownstream_gene_variant
COCA-CN4155462188155462188single base substitutionACintron_variant
COCA-CN4155462188155462188single base substitutionACupstream_gene_variant
COCA-CN4155463420155463420single base substitutionCT3_prime_UTR_variant
COCA-CN4155463420155463420single base substitutionCTdownstream_gene_variant
COCA-CN4155463420155463420single base substitutionCTexon_variant
COCA-CN4155463420155463420single base substitutionCTsynonymous_variantG193G579G>A
COCA-CN4155463420155463420single base substitutionCTsynonymous_variantG200G600G>A
COCA-CN4155463420155463420single base substitutionCTsynonymous_variantG202G606G>A
COCA-CN4155463420155463420single base substitutionCTupstream_gene_variant
COCA-CN4155468886155468886single base substitutionTA3_prime_UTR_variant
COCA-CN4155468886155468886single base substitutionTAexon_variant
COCA-CN4155468886155468886single base substitutionTAmissense_variantH77L230A>T
COCA-CN4155468886155468886single base substitutionTAmissense_variantH79L236A>T
COCA-CN4155468886155468886single base substitutionTAupstream_gene_variant
COCA-CN4155470051155470051single base substitutionTCexon_variant
COCA-CN4155470051155470051single base substitutionTCmissense_variantR14G40A>G
COCA-CN4155470051155470051single base substitutionTCmissense_variantR16G46A>G
COCA-CN4155470051155470051single base substitutionTCupstream_gene_variant
COCA-CN4155470706155470706single base substitutionCGintron_variant
COCA-CN4155470706155470706single base substitutionCGupstream_gene_variant
COCA-CN4155471049155471049single base substitutionGTintron_variant
COCA-CN4155471049155471049single base substitutionGTupstream_gene_variant
ESAD-UK4155451194155451194single base substitutionGAdownstream_gene_variant
ESAD-UK4155451572155451572single base substitutionCTdownstream_gene_variant
ESAD-UK4155452064155452064single base substitutionACdownstream_gene_variant
ESAD-UK4155452150155452150single base substitutionGAdownstream_gene_variant
ESAD-UK4155452498155452498single base substitutionGAdownstream_gene_variant
ESAD-UK4155455711155455711single base substitutionGCdownstream_gene_variant
ESAD-UK4155455895155455895single base substitutionGAdownstream_gene_variant
ESAD-UK4155457364155457364single base substitutionTA3_prime_UTR_variant
ESAD-UK4155457364155457364single base substitutionTAdownstream_gene_variant
ESAD-UK4155457530155457530single base substitutionTA3_prime_UTR_variant
ESAD-UK4155457530155457530single base substitutionTAdownstream_gene_variant
ESAD-UK4155462468155462468single base substitutionAGdownstream_gene_variant
ESAD-UK4155462468155462468single base substitutionAGintron_variant
ESAD-UK4155462468155462468single base substitutionAGupstream_gene_variant
ESAD-UK4155464991155464991single base substitutionTAdownstream_gene_variant
ESAD-UK4155464991155464991single base substitutionTAintron_variant
ESAD-UK4155464991155464991single base substitutionTAupstream_gene_variant
ESAD-UK4155465250155465250single base substitutionGAdownstream_gene_variant
ESAD-UK4155465250155465250single base substitutionGAintron_variant
ESAD-UK4155465250155465250single base substitutionGAupstream_gene_variant
ESAD-UK4155466670155466670single base substitutionATdownstream_gene_variant
ESAD-UK4155466670155466670single base substitutionATintron_variant
ESAD-UK4155466670155466670single base substitutionATupstream_gene_variant
ESAD-UK4155468303155468303single base substitutionTGdownstream_gene_variant
ESAD-UK4155468303155468303single base substitutionTGintron_variant
ESAD-UK4155468303155468303single base substitutionTGupstream_gene_variant
ESAD-UK4155469674155469674single base substitutionTAintron_variant
ESAD-UK4155469674155469674single base substitutionTAupstream_gene_variant
ESAD-UK4155471580155471580single base substitutionAG5_prime_UTR_premature_start_codon_gain_variant
ESAD-UK4155471580155471580single base substitutionAGupstream_gene_variant
ESAD-UK4155471638155471638single base substitutionCTupstream_gene_variant
ESAD-UK4155473263155473263single base substitutionGAupstream_gene_variant
ESAD-UK4155475289155475289single base substitutionCTupstream_gene_variant
ESAD-UK4155476342155476342single base substitutionGAupstream_gene_variant
ESCA-CN4155461113155461113single base substitutionTCdownstream_gene_variant
ESCA-CN4155461113155461113single base substitutionTCexon_variant
ESCA-CN4155461113155461113single base substitutionTCsynonymous_variantQ335Q1005A>G
ESCA-CN4155461113155461113single base substitutionTCsynonymous_variantQ344Q1032A>G
ESCA-CN4155461113155461113single base substitutionTCupstream_gene_variant
ESCA-CN4155461687155461687single base substitutionACdownstream_gene_variant
ESCA-CN4155461687155461687single base substitutionACintron_variant
ESCA-CN4155461687155461687single base substitutionACupstream_gene_variant
KIRP-US4155465648155465648single base substitutionTC3_prime_UTR_variant
KIRP-US4155465648155465648single base substitutionTCdownstream_gene_variant
KIRP-US4155465648155465648single base substitutionTCexon_variant
KIRP-US4155465648155465648single base substitutionTCsynonymous_variantK172K516A>G
KIRP-US4155465648155465648single base substitutionTCsynonymous_variantK179K537A>G
KIRP-US4155465648155465648single base substitutionTCsynonymous_variantK181K543A>G
KIRP-US4155465648155465648single base substitutionTCupstream_gene_variant
KIRP-US4155470082155470082single base substitutionTCexon_variant
KIRP-US4155470082155470082single base substitutionTCsynonymous_variantV3V9A>G
KIRP-US4155470082155470082single base substitutionTCsynonymous_variantV5V15A>G
KIRP-US4155470082155470082single base substitutionTCupstream_gene_variant
LAML-KR4155459194155459194single base substitutionAT3_prime_UTR_variant
LAML-KR4155459194155459194single base substitutionATdownstream_gene_variant
LAML-KR4155459194155459194single base substitutionATsynonymous_variantI397I1191T>A
LAML-KR4155459194155459194single base substitutionATsynonymous_variantI406I1218T>A
LAML-KR4155459194155459194single base substitutionATsynonymous_variantI49I147T>A
LAML-KR4155459194155459194single base substitutionATupstream_gene_variant
LAML-KR4155461113155461113single base substitutionTCdownstream_gene_variant
LAML-KR4155461113155461113single base substitutionTCexon_variant
LAML-KR4155461113155461113single base substitutionTCsynonymous_variantQ335Q1005A>G
LAML-KR4155461113155461113single base substitutionTCsynonymous_variantQ344Q1032A>G
LAML-KR4155461113155461113single base substitutionTCupstream_gene_variant
LAML-KR4155466935155466935single base substitutionTCdownstream_gene_variant
LAML-KR4155466935155466935single base substitutionTCintron_variant
LAML-KR4155466935155466935single base substitutionTCupstream_gene_variant
LICA-FR4155452921155452921single base substitutionGCdownstream_gene_variant
LICA-FR4155471372155471372single base substitutionTCintron_variant
LICA-FR4155471372155471372single base substitutionTCupstream_gene_variant
LINC-JP4155457794155457794single base substitutionAT3_prime_UTR_variant
LINC-JP4155457794155457794single base substitutionATdownstream_gene_variant
LINC-JP4155457794155457794single base substitutionATexon_variant
LINC-JP4155467188155467188single base substitutionTCdownstream_gene_variant
LINC-JP4155467188155467188single base substitutionTCexon_variant
LINC-JP4155467188155467188single base substitutionTCintron_variant
LINC-JP4155467188155467188single base substitutionTCupstream_gene_variant
LIRI-JP4155451458155451458single base substitutionGAdownstream_gene_variant
LIRI-JP4155452718155452718single base substitutionTCdownstream_gene_variant
LIRI-JP4155452756155452756single base substitutionACdownstream_gene_variant
LIRI-JP4155455181155455181single base substitutionGAdownstream_gene_variant
LIRI-JP4155458904155458904single base substitutionTAdownstream_gene_variant
LIRI-JP4155458904155458904single base substitutionTAintron_variant
LIRI-JP4155458904155458904single base substitutionTAupstream_gene_variant
LIRI-JP4155460466155460466single base substitutionACdownstream_gene_variant
LIRI-JP4155460466155460466single base substitutionACintron_variant
LIRI-JP4155460466155460466single base substitutionACupstream_gene_variant
LIRI-JP4155460615155460615single base substitutionAGdownstream_gene_variant
LIRI-JP4155460615155460615single base substitutionAGintron_variant
LIRI-JP4155460615155460615single base substitutionAGupstream_gene_variant
LIRI-JP4155460734155460734single base substitutionTGdownstream_gene_variant
LIRI-JP4155460734155460734single base substitutionTGintron_variant
LIRI-JP4155460734155460734single base substitutionTGupstream_gene_variant
LIRI-JP4155463359155463359single base substitutionAG3_prime_UTR_variant
LIRI-JP4155463359155463359single base substitutionAGdownstream_gene_variant
LIRI-JP4155463359155463359single base substitutionAGexon_variant
LIRI-JP4155463359155463359single base substitutionAGmissense_variantS214P640T>C
LIRI-JP4155463359155463359single base substitutionAGmissense_variantS223P667T>C
LIRI-JP4155463359155463359single base substitutionAGupstream_gene_variant
LIRI-JP4155463877155463877single base substitutionTCdownstream_gene_variant
LIRI-JP4155463877155463877single base substitutionTCintron_variant
LIRI-JP4155463877155463877single base substitutionTCupstream_gene_variant
LIRI-JP4155468052155468052single base substitutionCAdownstream_gene_variant
LIRI-JP4155468052155468052single base substitutionCAexon_variant
LIRI-JP4155468052155468052single base substitutionCAintron_variant
LIRI-JP4155468052155468052single base substitutionCAupstream_gene_variant
LIRI-JP4155468745155468745single base substitutionCTexon_variant
LIRI-JP4155468745155468745single base substitutionCTintron_variant
LIRI-JP4155468745155468745single base substitutionCTupstream_gene_variant
LIRI-JP4155471901155471901single base substitutionGTupstream_gene_variant
LIRI-JP4155472924155472924single base substitutionAGupstream_gene_variant
LIRI-JP4155475979155475979single base substitutionACupstream_gene_variant
LUSC-KR4155454429155454429single base substitutionTCdownstream_gene_variant
LUSC-KR4155454883155454883single base substitutionGAdownstream_gene_variant
LUSC-KR4155460459155460459single base substitutionTCdownstream_gene_variant
LUSC-KR4155460459155460459single base substitutionTCintron_variant
LUSC-KR4155460459155460459single base substitutionTCupstream_gene_variant
LUSC-KR4155469662155469662single base substitutionTAintron_variant
LUSC-KR4155469662155469662single base substitutionTAupstream_gene_variant
LUSC-US4155458514155458514single base substitutionAG3_prime_UTR_variant
LUSC-US4155458514155458514single base substitutionAGdownstream_gene_variant
LUSC-US4155458514155458514single base substitutionAGexon_variant
LUSC-US4155458514155458514single base substitutionAGintron_variant
LUSC-US4155458514155458514single base substitutionAGmissense_variantF461S1382T>C
LUSC-US4155458514155458514single base substitutionAGmissense_variantF470S1409T>C
LUSC-US4155459240155459240single base substitutionGCdownstream_gene_variant
LUSC-US4155459240155459240single base substitutionGCmissense_variantS34C101C>G
LUSC-US4155459240155459240single base substitutionGCmissense_variantS382C1145C>G
LUSC-US4155459240155459240single base substitutionGCmissense_variantS391C1172C>G
LUSC-US4155459240155459240single base substitutionGCsplice_region_variant
LUSC-US4155459240155459240single base substitutionGCupstream_gene_variant
LUSC-US4155460272155460272single base substitutionAGdownstream_gene_variant
LUSC-US4155460272155460272single base substitutionAGexon_variant
LUSC-US4155460272155460272single base substitutionAGmissense_variantV22A65T>C
LUSC-US4155460272155460272single base substitutionAGmissense_variantV370A1109T>C
LUSC-US4155460272155460272single base substitutionAGmissense_variantV379A1136T>C
LUSC-US4155460272155460272single base substitutionAGupstream_gene_variant
LUSC-US4155461791155461791single base substitutionCAdownstream_gene_variant
LUSC-US4155461791155461791single base substitutionCAexon_variant
LUSC-US4155461791155461791single base substitutionCAsynonymous_variantP289P867G>T
LUSC-US4155461791155461791single base substitutionCAsynonymous_variantP298P894G>T
LUSC-US4155461791155461791single base substitutionCAupstream_gene_variant
LUSC-US4155467044155467044single base substitutionTCdownstream_gene_variant
LUSC-US4155467044155467044single base substitutionTCexon_variant
LUSC-US4155467044155467044single base substitutionTCmissense_variantS137G409A>G
LUSC-US4155467044155467044single base substitutionTCmissense_variantS144G430A>G
LUSC-US4155467044155467044single base substitutionTCmissense_variantS146G436A>G
LUSC-US4155467044155467044single base substitutionTCupstream_gene_variant
LUSC-US4155467273155467273single base substitutionATdownstream_gene_variant
LUSC-US4155467273155467273single base substitutionATexon_variant
LUSC-US4155467273155467273single base substitutionATintron_variant
LUSC-US4155467273155467273single base substitutionATsplice_donor_variant
LUSC-US4155467273155467273single base substitutionATupstream_gene_variant
MALY-DE4155451834155451834single base substitutionACdownstream_gene_variant
MALY-DE4155454371155454371single base substitutionGTdownstream_gene_variant
MALY-DE4155459153155459153single base substitutionGA3_prime_UTR_variant
MALY-DE4155459153155459153single base substitutionGAdownstream_gene_variant
MALY-DE4155459153155459153single base substitutionGAmissense_variantT411M1232C>T
MALY-DE4155459153155459153single base substitutionGAmissense_variantT420M1259C>T
MALY-DE4155459153155459153single base substitutionGAmissense_variantT63M188C>T
MALY-DE4155459153155459153single base substitutionGAupstream_gene_variant
MALY-DE4155462215155462215single base substitutionAGdownstream_gene_variant
MALY-DE4155462215155462215single base substitutionAGintron_variant
MALY-DE4155462215155462215single base substitutionAGupstream_gene_variant
MALY-DE4155462242155462242single base substitutionAGdownstream_gene_variant
MALY-DE4155462242155462242single base substitutionAGintron_variant
MALY-DE4155462242155462242single base substitutionAGupstream_gene_variant
MALY-DE4155462897155462897single base substitutionTAdownstream_gene_variant
MALY-DE4155462897155462897single base substitutionTAintron_variant
MALY-DE4155462897155462897single base substitutionTAupstream_gene_variant
MALY-DE4155467704155467704single base substitutionCTdownstream_gene_variant
MALY-DE4155467704155467704single base substitutionCTexon_variant
MALY-DE4155467704155467704single base substitutionCTintron_variant
MALY-DE4155467704155467704single base substitutionCTupstream_gene_variant
MALY-DE4155475673155475673single base substitutionTAupstream_gene_variant
MALY-DE4155475701155475701single base substitutionTAupstream_gene_variant
MALY-DE4155475711155475711single base substitutionTCupstream_gene_variant
MELA-AU4155451625155451625single base substitutionATdownstream_gene_variant
MELA-AU4155451891155451891single base substitutionCTdownstream_gene_variant
MELA-AU4155451895155451895single base substitutionAGdownstream_gene_variant
MELA-AU4155451984155451984single base substitutionGAdownstream_gene_variant
MELA-AU4155452320155452320single base substitutionGAdownstream_gene_variant
MELA-AU4155452347155452347single base substitutionGAdownstream_gene_variant
MELA-AU4155452481155452481single base substitutionACdownstream_gene_variant
MELA-AU4155453529155453529single base substitutionGAdownstream_gene_variant
MELA-AU4155453727155453727single base substitutionCTdownstream_gene_variant
MELA-AU4155454015155454015insertion of <=200bp-Adownstream_gene_variant
MELA-AU4155454249155454249single base substitutionGAdownstream_gene_variant
MELA-AU4155454250155454250single base substitutionGAdownstream_gene_variant
MELA-AU4155454831155454831single base substitutionCTdownstream_gene_variant
MELA-AU4155454909155454909single base substitutionGAdownstream_gene_variant
MELA-AU4155455016155455016single base substitutionCTdownstream_gene_variant
MELA-AU4155455342155455342single base substitutionGAdownstream_gene_variant
MELA-AU4155455431155455431single base substitutionGAdownstream_gene_variant
MELA-AU4155455814155455814single base substitutionGAdownstream_gene_variant
MELA-AU4155456053155456053single base substitutionCTdownstream_gene_variant
MELA-AU4155457425155457425single base substitutionAT3_prime_UTR_variant
MELA-AU4155457425155457425single base substitutionATdownstream_gene_variant
MELA-AU4155457538155457538single base substitutionGA3_prime_UTR_variant
MELA-AU4155457538155457538single base substitutionGAdownstream_gene_variant
MELA-AU4155457906155457906single base substitutionGAdownstream_gene_variant
MELA-AU4155457906155457906single base substitutionGAintron_variant
MELA-AU4155458076155458076single base substitutionGAdownstream_gene_variant
MELA-AU4155458076155458076single base substitutionGAintron_variant
MELA-AU4155458416155458416single base substitutionGAdownstream_gene_variant
MELA-AU4155458416155458416single base substitutionGAintron_variant
MELA-AU4155458720155458720single base substitutionGAdownstream_gene_variant
MELA-AU4155458720155458720single base substitutionGAintron_variant
MELA-AU4155458720155458720single base substitutionGAupstream_gene_variant
MELA-AU4155459005155459006multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU4155459005155459006multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU4155459005155459006multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU4155459187155459187single base substitutionGA3_prime_UTR_variant
MELA-AU4155459187155459187single base substitutionGAdownstream_gene_variant
MELA-AU4155459187155459187single base substitutionGAmissense_variantL400F1198C>T
MELA-AU4155459187155459187single base substitutionGAmissense_variantL409F1225C>T
MELA-AU4155459187155459187single base substitutionGAmissense_variantL52F154C>T
MELA-AU4155459187155459187single base substitutionGAupstream_gene_variant
MELA-AU4155460406155460406single base substitutionGAdownstream_gene_variant
MELA-AU4155460406155460406single base substitutionGAintron_variant
MELA-AU4155460406155460406single base substitutionGAupstream_gene_variant
MELA-AU4155460643155460643single base substitutionGAdownstream_gene_variant
MELA-AU4155460643155460643single base substitutionGAintron_variant
MELA-AU4155460643155460643single base substitutionGAupstream_gene_variant
MELA-AU4155460939155460939single base substitutionGAdownstream_gene_variant
MELA-AU4155460939155460939single base substitutionGAintron_variant
MELA-AU4155460939155460939single base substitutionGAupstream_gene_variant
MELA-AU4155461027155461027single base substitutionGAdownstream_gene_variant
MELA-AU4155461027155461027single base substitutionGAintron_variant
MELA-AU4155461027155461027single base substitutionGAupstream_gene_variant
MELA-AU4155461057155461057single base substitutionGAdownstream_gene_variant
MELA-AU4155461057155461057single base substitutionGAintron_variant
MELA-AU4155461057155461057single base substitutionGAupstream_gene_variant
MELA-AU4155461560155461560single base substitutionGAdownstream_gene_variant
MELA-AU4155461560155461560single base substitutionGAintron_variant
MELA-AU4155461560155461560single base substitutionGAupstream_gene_variant
MELA-AU4155461785155461785single base substitutionGAdownstream_gene_variant
MELA-AU4155461785155461785single base substitutionGAexon_variant
MELA-AU4155461785155461785single base substitutionGAsynonymous_variantI291I873C>T
MELA-AU4155461785155461785single base substitutionGAsynonymous_variantI300I900C>T
MELA-AU4155461785155461785single base substitutionGAupstream_gene_variant
MELA-AU4155461935155461935single base substitutionAGdownstream_gene_variant
MELA-AU4155461935155461935single base substitutionAGsplice_donor_variant
MELA-AU4155461935155461935single base substitutionAGupstream_gene_variant
MELA-AU4155462181155462181single base substitutionATdownstream_gene_variant
MELA-AU4155462181155462181single base substitutionATintron_variant
MELA-AU4155462181155462181single base substitutionATupstream_gene_variant
MELA-AU4155462184155462184single base substitutionGAdownstream_gene_variant
MELA-AU4155462184155462184single base substitutionGAintron_variant
MELA-AU4155462184155462184single base substitutionGAupstream_gene_variant
MELA-AU4155462915155462915single base substitutionGAdownstream_gene_variant
MELA-AU4155462915155462915single base substitutionGAintron_variant
MELA-AU4155462915155462915single base substitutionGAupstream_gene_variant
MELA-AU4155463894155463894single base substitutionGAdownstream_gene_variant
MELA-AU4155463894155463894single base substitutionGAintron_variant
MELA-AU4155463894155463894single base substitutionGAupstream_gene_variant
MELA-AU4155465797155465797single base substitutionGAdownstream_gene_variant
MELA-AU4155465797155465797single base substitutionGAintron_variant
MELA-AU4155465797155465797single base substitutionGAupstream_gene_variant
MELA-AU4155465942155465942single base substitutionGCdownstream_gene_variant
MELA-AU4155465942155465942single base substitutionGCintron_variant
MELA-AU4155465942155465942single base substitutionGCupstream_gene_variant
MELA-AU4155466089155466089single base substitutionTAdownstream_gene_variant
MELA-AU4155466089155466089single base substitutionTAintron_variant
MELA-AU4155466089155466089single base substitutionTAupstream_gene_variant
MELA-AU4155467304155467305multiple base substitution (>=2bp and <=200bp)GGAA3_prime_UTR_variant
MELA-AU4155467304155467305multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU4155467304155467305multiple base substitution (>=2bp and <=200bp)GGAAexon_variant
MELA-AU4155467304155467305multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU4155467304155467305multiple base substitution (>=2bp and <=200bp)GGAAmissense_variantS116F347CC>TT
MELA-AU4155467304155467305multiple base substitution (>=2bp and <=200bp)GGAAmissense_variantS123F368CC>TT
MELA-AU4155467304155467305multiple base substitution (>=2bp and <=200bp)GGAAmissense_variantS125F374CC>TT
MELA-AU4155467304155467305multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU4155467451155467451single base substitutionACdownstream_gene_variant
MELA-AU4155467451155467451single base substitutionACintron_variant
MELA-AU4155467451155467451single base substitutionACupstream_gene_variant
MELA-AU4155467834155467834single base substitutionCTdownstream_gene_variant
MELA-AU4155467834155467834single base substitutionCTexon_variant
MELA-AU4155467834155467834single base substitutionCTintron_variant
MELA-AU4155467834155467834single base substitutionCTupstream_gene_variant
MELA-AU4155468911155468911single base substitutionGT3_prime_UTR_variant
MELA-AU4155468911155468911single base substitutionGTexon_variant
MELA-AU4155468911155468911single base substitutionGTmissense_variantQ69K205C>A
MELA-AU4155468911155468911single base substitutionGTmissense_variantQ71K211C>A
MELA-AU4155468911155468911single base substitutionGTupstream_gene_variant
MELA-AU4155468961155468961single base substitutionGA3_prime_UTR_variant
MELA-AU4155468961155468961single base substitutionGAexon_variant
MELA-AU4155468961155468961single base substitutionGAmissense_variantP52L155C>T
MELA-AU4155468961155468961single base substitutionGAmissense_variantP54L161C>T
MELA-AU4155468961155468961single base substitutionGAupstream_gene_variant
MELA-AU4155469143155469143single base substitutionGAintron_variant
MELA-AU4155469143155469143single base substitutionGAupstream_gene_variant
MELA-AU4155469504155469504single base substitutionGAintron_variant
MELA-AU4155469504155469504single base substitutionGAupstream_gene_variant
MELA-AU4155470543155470543single base substitutionTAintron_variant
MELA-AU4155470543155470543single base substitutionTAupstream_gene_variant
MELA-AU4155470617155470617single base substitutionATintron_variant
MELA-AU4155470617155470617single base substitutionATupstream_gene_variant
MELA-AU4155471363155471363single base substitutionGAintron_variant
MELA-AU4155471363155471363single base substitutionGAupstream_gene_variant
MELA-AU4155471542155471542single base substitutionCT5_prime_UTR_variant
MELA-AU4155471542155471542single base substitutionCTexon_variant
MELA-AU4155471542155471542single base substitutionCTupstream_gene_variant
MELA-AU4155471584155471585multiple base substitution (>=2bp and <=200bp)CTTC5_prime_UTR_variant
MELA-AU4155471584155471585multiple base substitution (>=2bp and <=200bp)CTTCupstream_gene_variant
MELA-AU4155471698155471698single base substitutionGAupstream_gene_variant
MELA-AU4155472131155472131single base substitutionCTupstream_gene_variant
MELA-AU4155473110155473110single base substitutionCTupstream_gene_variant
MELA-AU4155473735155473735single base substitutionCTupstream_gene_variant
MELA-AU4155474098155474098single base substitutionGAupstream_gene_variant
MELA-AU4155474342155474342single base substitutionGAupstream_gene_variant
MELA-AU4155474347155474347single base substitutionAGupstream_gene_variant
MELA-AU4155474376155474376single base substitutionCTupstream_gene_variant
MELA-AU4155474718155474718single base substitutionCTupstream_gene_variant
MELA-AU4155475008155475008single base substitutionGAupstream_gene_variant
MELA-AU4155475066155475066single base substitutionCTupstream_gene_variant
MELA-AU4155475150155475150single base substitutionTCupstream_gene_variant
MELA-AU4155475178155475178single base substitutionCTupstream_gene_variant
MELA-AU4155475643155475643single base substitutionGAupstream_gene_variant
MELA-AU4155475704155475704single base substitutionTGupstream_gene_variant
MELA-AU4155475868155475868single base substitutionCTupstream_gene_variant
MELA-AU4155475942155475942single base substitutionCTupstream_gene_variant
MELA-AU4155476099155476099single base substitutionGAupstream_gene_variant
MELA-AU4155476263155476263single base substitutionGAupstream_gene_variant
ORCA-IN4155455942155455942single base substitutionTCdownstream_gene_variant
ORCA-IN4155472673155472673single base substitutionCGupstream_gene_variant
OV-AU4155453075155453075single base substitutionGCdownstream_gene_variant
OV-AU4155455254155455254single base substitutionTCdownstream_gene_variant
OV-AU4155466898155466898single base substitutionGCdownstream_gene_variant
OV-AU4155466898155466898single base substitutionGCintron_variant
OV-AU4155466898155466898single base substitutionGCupstream_gene_variant
PACA-AU4155453911155453911single base substitutionACdownstream_gene_variant
PACA-AU4155456186155456186single base substitutionCT3_prime_UTR_variant
PACA-AU4155456186155456186single base substitutionCTdownstream_gene_variant
PACA-AU4155458912155458912single base substitutionTCdownstream_gene_variant
PACA-AU4155458912155458912single base substitutionTCintron_variant
PACA-AU4155458912155458912single base substitutionTCupstream_gene_variant
PACA-AU4155462675155462675insertion of <=200bp-Adownstream_gene_variant
PACA-AU4155462675155462675insertion of <=200bp-Aintron_variant
PACA-AU4155462675155462675insertion of <=200bp-Aupstream_gene_variant
PACA-AU4155470782155470782single base substitutionAGintron_variant
PACA-AU4155470782155470782single base substitutionAGupstream_gene_variant
PACA-AU4155475780155475780single base substitutionGCupstream_gene_variant
PACA-CA4155452391155452391single base substitutionGAdownstream_gene_variant
PACA-CA4155453604155453604single base substitutionGCdownstream_gene_variant
PACA-CA4155454311155454311single base substitutionGTdownstream_gene_variant
PACA-CA4155457172155457172single base substitutionCG3_prime_UTR_variant
PACA-CA4155457172155457172single base substitutionCGdownstream_gene_variant
PACA-CA4155457324155457324single base substitutionTC3_prime_UTR_variant
PACA-CA4155457324155457324single base substitutionTCdownstream_gene_variant
PACA-CA4155461799155461799single base substitutionAGdownstream_gene_variant
PACA-CA4155461799155461799single base substitutionAGexon_variant
PACA-CA4155461799155461799single base substitutionAGsynonymous_variantL287L859T>C
PACA-CA4155461799155461799single base substitutionAGsynonymous_variantL296L886T>C
PACA-CA4155461799155461799single base substitutionAGupstream_gene_variant
PACA-CA4155465909155465909single base substitutionGAdownstream_gene_variant
PACA-CA4155465909155465909single base substitutionGAintron_variant
PACA-CA4155465909155465909single base substitutionGAupstream_gene_variant
PACA-CA4155466762155466762single base substitutionCTdownstream_gene_variant
PACA-CA4155466762155466762single base substitutionCTintron_variant
PACA-CA4155466762155466762single base substitutionCTupstream_gene_variant
PACA-CA4155466843155466843single base substitutionAGdownstream_gene_variant
PACA-CA4155466843155466843single base substitutionAGintron_variant
PACA-CA4155466843155466843single base substitutionAGupstream_gene_variant
PBCA-DE4155473048155473048insertion of <=200bp-ATupstream_gene_variant
PBCA-DE4155474117155474117single base substitutionCAupstream_gene_variant
PBCA-DE4155475293155475293single base substitutionGAupstream_gene_variant
PRAD-CA4155457402155457402single base substitutionAG3_prime_UTR_variant
PRAD-CA4155457402155457402single base substitutionAGdownstream_gene_variant
PRAD-CA4155464895155464895single base substitutionGCdownstream_gene_variant
PRAD-CA4155464895155464895single base substitutionGCintron_variant
PRAD-CA4155464895155464895single base substitutionGCupstream_gene_variant
PRAD-UK4155460948155460948single base substitutionTAdownstream_gene_variant
PRAD-UK4155460948155460948single base substitutionTAintron_variant
PRAD-UK4155460948155460948single base substitutionTAupstream_gene_variant
PRAD-UK4155476133155476133single base substitutionCTupstream_gene_variant
RECA-EU4155453359155453359single base substitutionGTdownstream_gene_variant
RECA-EU4155455794155455794single base substitutionATdownstream_gene_variant
RECA-EU4155459439155459439single base substitutionCAdownstream_gene_variant
RECA-EU4155459439155459439single base substitutionCAintron_variant
RECA-EU4155459439155459439single base substitutionCAupstream_gene_variant
RECA-EU4155460213155460213single base substitutionACdownstream_gene_variant
RECA-EU4155460213155460213single base substitutionACexon_variant
RECA-EU4155460213155460213single base substitutionACintron_variant
RECA-EU4155460213155460213single base substitutionACupstream_gene_variant
RECA-EU4155467604155467604single base substitutionGCdownstream_gene_variant
RECA-EU4155467604155467604single base substitutionGCintron_variant
RECA-EU4155467604155467604single base substitutionGCupstream_gene_variant
RECA-EU4155473431155473431single base substitutionTAupstream_gene_variant
RECA-EU4155475353155475353single base substitutionTCupstream_gene_variant
SKCA-BR4155451788155451788single base substitutionCTdownstream_gene_variant
SKCA-BR4155452054155452054single base substitutionAGdownstream_gene_variant
SKCA-BR4155454546155454546insertion of <=200bp-ATATATdownstream_gene_variant
SKCA-BR4155454572155454572single base substitutionCTdownstream_gene_variant
SKCA-BR4155457183155457183single base substitutionTC3_prime_UTR_variant
SKCA-BR4155457183155457183single base substitutionTCdownstream_gene_variant
SKCA-BR4155463838155463838single base substitutionGAdownstream_gene_variant
SKCA-BR4155463838155463838single base substitutionGAintron_variant
SKCA-BR4155463838155463838single base substitutionGAupstream_gene_variant
SKCA-BR4155468075155468075single base substitutionATdownstream_gene_variant
SKCA-BR4155468075155468075single base substitutionATexon_variant
SKCA-BR4155468075155468075single base substitutionATintron_variant
SKCA-BR4155468075155468075single base substitutionATupstream_gene_variant
SKCA-BR4155473095155473095single base substitutionTAupstream_gene_variant
SKCA-BR4155473816155473816single base substitutionAGupstream_gene_variant
SKCA-BR4155475526155475526insertion of <=200bp-TGTGTGAupstream_gene_variant
SKCA-BR4155476231155476231single base substitutionCTupstream_gene_variant
SKCA-BR4155476404155476404single base substitutionGAupstream_gene_variant
SKCM-US4155458438155458438single base substitutionGAdownstream_gene_variant
SKCM-US4155458438155458438single base substitutionGAintron_variant
SKCM-US4155458438155458438single base substitutionGAsplice_region_variant
SKCM-US4155460287155460287single base substitutionGAdownstream_gene_variant
SKCM-US4155460287155460287single base substitutionGAexon_variant
SKCM-US4155460287155460287single base substitutionGAmissense_variantS17L50C>T
SKCM-US4155460287155460287single base substitutionGAmissense_variantS365L1094C>T
SKCM-US4155460287155460287single base substitutionGAmissense_variantS374L1121C>T
SKCM-US4155460287155460287single base substitutionGAupstream_gene_variant
SKCM-US4155461135155461135single base substitutionCTdownstream_gene_variant
SKCM-US4155461135155461135single base substitutionCTexon_variant
SKCM-US4155461135155461135single base substitutionCTmissense_variantR328K983G>A
SKCM-US4155461135155461135single base substitutionCTmissense_variantR337K1010G>A
SKCM-US4155461135155461135single base substitutionCTupstream_gene_variant
SKCM-US4155461949155461949single base substitutionGA3_prime_UTR_variant
SKCM-US4155461949155461949single base substitutionGAdownstream_gene_variant
SKCM-US4155461949155461949single base substitutionGAexon_variant
SKCM-US4155461949155461949single base substitutionGAsynonymous_variantL266L798C>T
SKCM-US4155461949155461949single base substitutionGAsynonymous_variantL275L825C>T
SKCM-US4155461949155461949single base substitutionGAupstream_gene_variant
SKCM-US4155461993155461993single base substitutionGA3_prime_UTR_variant
SKCM-US4155461993155461993single base substitutionGAdownstream_gene_variant
SKCM-US4155461993155461993single base substitutionGAexon_variant
SKCM-US4155461993155461993single base substitutionGAsynonymous_variantL252L754C>T
SKCM-US4155461993155461993single base substitutionGAsynonymous_variantL261L781C>T
SKCM-US4155461993155461993single base substitutionGAupstream_gene_variant
SKCM-US4155465644155465644single base substitutionGA3_prime_UTR_variant
SKCM-US4155465644155465644single base substitutionGAdownstream_gene_variant
SKCM-US4155465644155465644single base substitutionGAexon_variant
SKCM-US4155465644155465644single base substitutionGAmissense_variantP174S520C>T
SKCM-US4155465644155465644single base substitutionGAmissense_variantP181S541C>T
SKCM-US4155465644155465644single base substitutionGAmissense_variantP183S547C>T
SKCM-US4155465644155465644single base substitutionGAupstream_gene_variant
SKCM-US4155467365155467365single base substitutionCTdownstream_gene_variant
SKCM-US4155467365155467365single base substitutionCTintron_variant
SKCM-US4155467365155467365single base substitutionCTmissense_variantG103E308G>A
SKCM-US4155467365155467365single base substitutionCTmissense_variantG105E314G>A
SKCM-US4155467365155467365single base substitutionCTmissense_variantG96E287G>A
SKCM-US4155467365155467365single base substitutionCTsplice_region_variant
SKCM-US4155467365155467365single base substitutionCTupstream_gene_variant
SKCM-US4155469997155469997single base substitutionGA3_prime_UTR_variant
SKCM-US4155469997155469997single base substitutionGAexon_variant
SKCM-US4155469997155469997single base substitutionGAmissense_variantP32S94C>T
SKCM-US4155469997155469997single base substitutionGAmissense_variantP34S100C>T
SKCM-US4155469997155469997single base substitutionGAupstream_gene_variant
STAD-US4155458475155458475single base substitutionTC3_prime_UTR_variant
STAD-US4155458475155458475single base substitutionTCdownstream_gene_variant
STAD-US4155458475155458475single base substitutionTCexon_variant
STAD-US4155458475155458475single base substitutionTCintron_variant
STAD-US4155458475155458475single base substitutionTCmissense_variantD474G1421A>G
STAD-US4155458475155458475single base substitutionTCmissense_variantD483G1448A>G
STAD-US4155458569155458569single base substitutionCT3_prime_UTR_variant
STAD-US4155458569155458569single base substitutionCTdownstream_gene_variant
STAD-US4155458569155458569single base substitutionCTexon_variant
STAD-US4155458569155458569single base substitutionCTintron_variant
STAD-US4155458569155458569single base substitutionCTmissense_variantA443T1327G>A
STAD-US4155458569155458569single base substitutionCTmissense_variantA452T1354G>A
STAD-US4155459192155459192single base substitutionTA3_prime_UTR_variant
STAD-US4155459192155459192single base substitutionTAdownstream_gene_variant
STAD-US4155459192155459192single base substitutionTAmissense_variantQ398L1193A>T
STAD-US4155459192155459192single base substitutionTAmissense_variantQ407L1220A>T
STAD-US4155459192155459192single base substitutionTAmissense_variantQ50L149A>T
STAD-US4155459192155459192single base substitutionTAupstream_gene_variant
STAD-US4155460278155460278single base substitutionGTdownstream_gene_variant
STAD-US4155460278155460278single base substitutionGTexon_variant
STAD-US4155460278155460278single base substitutionGTmissense_variantA20D59C>A
STAD-US4155460278155460278single base substitutionGTmissense_variantA368D1103C>A
STAD-US4155460278155460278single base substitutionGTmissense_variantA377D1130C>A
STAD-US4155460278155460278single base substitutionGTupstream_gene_variant
STAD-US4155461124155461124single base substitutionCAdownstream_gene_variant
STAD-US4155461124155461124single base substitutionCAexon_variant
STAD-US4155461124155461124single base substitutionCAmissense_variantA332S994G>T
STAD-US4155461124155461124single base substitutionCAmissense_variantA341S1021G>T
STAD-US4155461124155461124single base substitutionCAupstream_gene_variant
STAD-US4155461762155461762single base substitutionCTdownstream_gene_variant
STAD-US4155461762155461762single base substitutionCTexon_variant
STAD-US4155461762155461762single base substitutionCTmissense_variantR299Q896G>A
STAD-US4155461762155461762single base substitutionCTmissense_variantR308Q923G>A
STAD-US4155461762155461762single base substitutionCTupstream_gene_variant
STAD-US4155463418155463418single base substitutionTC3_prime_UTR_variant
STAD-US4155463418155463418single base substitutionTCdownstream_gene_variant
STAD-US4155463418155463418single base substitutionTCexon_variant
STAD-US4155463418155463418single base substitutionTCmissense_variantH194R581A>G
STAD-US4155463418155463418single base substitutionTCmissense_variantH201R602A>G
STAD-US4155463418155463418single base substitutionTCmissense_variantH203R608A>G
STAD-US4155463418155463418single base substitutionTCupstream_gene_variant
STAD-US4155467035155467035single base substitutionGTdownstream_gene_variant
STAD-US4155467035155467035single base substitutionGTexon_variant
STAD-US4155467035155467035single base substitutionGTsynonymous_variantR140R418C>A
STAD-US4155467035155467035single base substitutionGTsynonymous_variantR147R439C>A
STAD-US4155467035155467035single base substitutionGTsynonymous_variantR149R445C>A
STAD-US4155467035155467035single base substitutionGTupstream_gene_variant
STAD-US4155468219155468219deletion of <=200bpA-downstream_gene_variant
STAD-US4155468219155468219deletion of <=200bpA-intron_variant
STAD-US4155468219155468219deletion of <=200bpA-splice_region_variant
STAD-US4155468219155468219deletion of <=200bpA-upstream_gene_variant
STAD-US4155468219155468219insertion of <=200bp-Adownstream_gene_variant
STAD-US4155468219155468219insertion of <=200bp-Aintron_variant
STAD-US4155468219155468219insertion of <=200bp-Asplice_region_variant
STAD-US4155468219155468219insertion of <=200bp-Aupstream_gene_variant
STAD-US4155468901155468901single base substitutionGA3_prime_UTR_variant
STAD-US4155468901155468901single base substitutionGAexon_variant
STAD-US4155468901155468901single base substitutionGAmissense_variantT72M215C>T
STAD-US4155468901155468901single base substitutionGAmissense_variantT74M221C>T
STAD-US4155468901155468901single base substitutionGAupstream_gene_variant
UCEC-US4155457811155457811single base substitutionAG3_prime_UTR_variant
UCEC-US4155457811155457811single base substitutionAGdownstream_gene_variant
UCEC-US4155457811155457811single base substitutionAGexon_variant
UCEC-US4155457811155457811single base substitutionAGsynonymous_variantL102L306T>C
UCEC-US4155457862155457862single base substitutionTG3_prime_UTR_variant
UCEC-US4155457862155457862single base substitutionTGdownstream_gene_variant
UCEC-US4155457862155457862single base substitutionTGexon_variant
UCEC-US4155457862155457862single base substitutionTGmissense_variantE498A1493A>C
UCEC-US4155457862155457862single base substitutionTGmissense_variantE507A1520A>C
UCEC-US4155457862155457862single base substitutionTGmissense_variantR85S255A>C
UCEC-US4155458497155458497single base substitutionGA3_prime_UTR_variant
UCEC-US4155458497155458497single base substitutionGAdownstream_gene_variant
UCEC-US4155458497155458497single base substitutionGAexon_variant
UCEC-US4155458497155458497single base substitutionGAintron_variant
UCEC-US4155458497155458497single base substitutionGAstop_gainedR467*1399C>T
UCEC-US4155458497155458497single base substitutionGAstop_gainedR476*1426C>T
UCEC-US4155459153155459153single base substitutionGA3_prime_UTR_variant
UCEC-US4155459153155459153single base substitutionGAdownstream_gene_variant
UCEC-US4155459153155459153single base substitutionGAmissense_variantT411M1232C>T
UCEC-US4155459153155459153single base substitutionGAmissense_variantT420M1259C>T
UCEC-US4155459153155459153single base substitutionGAmissense_variantT63M188C>T
UCEC-US4155459153155459153single base substitutionGAupstream_gene_variant
UCEC-US4155461175155461175single base substitutionGAdownstream_gene_variant
UCEC-US4155461175155461175single base substitutionGAexon_variant
UCEC-US4155461175155461175single base substitutionGAmissense_variantH315Y943C>T
UCEC-US4155461175155461175single base substitutionGAmissense_variantH324Y970C>T
UCEC-US4155461175155461175single base substitutionGAupstream_gene_variant
UCEC-US4155461763155461763single base substitutionGAdownstream_gene_variant
UCEC-US4155461763155461763single base substitutionGAexon_variant
UCEC-US4155461763155461763single base substitutionGAstop_gainedR299*895C>T
UCEC-US4155461763155461763single base substitutionGAstop_gainedR308*922C>T
UCEC-US4155461763155461763single base substitutionGAupstream_gene_variant
UCEC-US4155461949155461949single base substitutionGA3_prime_UTR_variant
UCEC-US4155461949155461949single base substitutionGAdownstream_gene_variant
UCEC-US4155461949155461949single base substitutionGAexon_variant
UCEC-US4155461949155461949single base substitutionGAsynonymous_variantL266L798C>T
UCEC-US4155461949155461949single base substitutionGAsynonymous_variantL275L825C>T
UCEC-US4155461949155461949single base substitutionGAupstream_gene_variant
UCEC-US4155462021155462021single base substitutionGA3_prime_UTR_variant
UCEC-US4155462021155462021single base substitutionGAdownstream_gene_variant
UCEC-US4155462021155462021single base substitutionGAexon_variant
UCEC-US4155462021155462021single base substitutionGAsynonymous_variantG242G726C>T
UCEC-US4155462021155462021single base substitutionGAsynonymous_variantG251G753C>T
UCEC-US4155462021155462021single base substitutionGAupstream_gene_variant
UCEC-US4155463404155463404single base substitutionGA3_prime_UTR_variant
UCEC-US4155463404155463404single base substitutionGAdownstream_gene_variant
UCEC-US4155463404155463404single base substitutionGAexon_variant
UCEC-US4155463404155463404single base substitutionGAstop_gainedR199*595C>T
UCEC-US4155463404155463404single base substitutionGAstop_gainedR206*616C>T
UCEC-US4155463404155463404single base substitutionGAstop_gainedR208*622C>T
UCEC-US4155463404155463404single base substitutionGAupstream_gene_variant
UCEC-US4155463411155463411single base substitutionGA3_prime_UTR_variant
UCEC-US4155463411155463411single base substitutionGAdownstream_gene_variant
UCEC-US4155463411155463411single base substitutionGAexon_variant
UCEC-US4155463411155463411single base substitutionGAsynonymous_variantG196G588C>T
UCEC-US4155463411155463411single base substitutionGAsynonymous_variantG203G609C>T
UCEC-US4155463411155463411single base substitutionGAsynonymous_variantG205G615C>T
UCEC-US4155463411155463411single base substitutionGAupstream_gene_variant
UCEC-US4155463420155463420single base substitutionCT3_prime_UTR_variant
UCEC-US4155463420155463420single base substitutionCTdownstream_gene_variant
UCEC-US4155463420155463420single base substitutionCTexon_variant
UCEC-US4155463420155463420single base substitutionCTsynonymous_variantG193G579G>A
UCEC-US4155463420155463420single base substitutionCTsynonymous_variantG200G600G>A
UCEC-US4155463420155463420single base substitutionCTsynonymous_variantG202G606G>A
UCEC-US4155463420155463420single base substitutionCTupstream_gene_variant
UCEC-US4155465672155465672single base substitutionCA3_prime_UTR_variant
UCEC-US4155465672155465672single base substitutionCAdownstream_gene_variant
UCEC-US4155465672155465672single base substitutionCAexon_variant
UCEC-US4155465672155465672single base substitutionCAmissense_variantK164N492G>T
UCEC-US4155465672155465672single base substitutionCAmissense_variantK171N513G>T
UCEC-US4155465672155465672single base substitutionCAmissense_variantK173N519G>T
UCEC-US4155465672155465672single base substitutionCAupstream_gene_variant
UCEC-US4155467062155467062single base substitutionGAdownstream_gene_variant
UCEC-US4155467062155467062single base substitutionGAexon_variant
UCEC-US4155467062155467062single base substitutionGAmissense_variantR131C391C>T
UCEC-US4155467062155467062single base substitutionGAmissense_variantR138C412C>T
UCEC-US4155467062155467062single base substitutionGAmissense_variantR140C418C>T
UCEC-US4155467062155467062single base substitutionGAupstream_gene_variant
UCEC-US4155468997155468997single base substitutionCA3_prime_UTR_variant
UCEC-US4155468997155468997single base substitutionCAexon_variant
UCEC-US4155468997155468997single base substitutionCAmissense_variantR40L119G>T
UCEC-US4155468997155468997single base substitutionCAmissense_variantR42L125G>T
UCEC-US4155468997155468997single base substitutionCAupstream_gene_variant
UCEC-US4155470047155470047single base substitutionGAexon_variant
UCEC-US4155470047155470047single base substitutionGAmissense_variantS15L44C>T
UCEC-US4155470047155470047single base substitutionGAmissense_variantS17L50C>T
UCEC-US4155470047155470047single base substitutionGAupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-EE-A29V-06COSM3601125c.314G>Ap.G105ESubstitution - Missense4:154546213-154546213-
T3503COSM4715834c.939+1G>Ap.?Unknown4:154540593-154540593-
I2L-P19Ta-Tumor-BiopsyCOSM4715836c.260-3_260-2insTp.?Unknown4:154547066-154547067-
CN-AML-08-TCOSM3760448c.1218T>Ap.I406ISubstitution - coding silent4:154538042-154538042-
TCGA-AN-A0AK-01COSM3825423c.548C>Ap.P183HSubstitution - Missense4:154544491-154544491-
46MCOSM5588679c.1042+1G>Ap.?Unknown4:154539950-154539950-
TCGA-BS-A0UV-01COSM1052387c.825C>Tp.L275LSubstitution - coding silent4:154540797-154540797-
CSCC-27-TCOSM1428102c.145C>Tp.R49CSubstitution - Missense4:154547825-154547825-
TCGA-BR-8059-01COSM4122939c.923G>Ap.R308QSubstitution - Missense4:154540610-154540610-
TCGA-JW-A5VJ-01COSM4818501c.82G>Ap.D28NSubstitution - Missense4:154548863-154548863-
T407COSM4715838c.72G>Ap.M24ISubstitution - Missense4:154548873-154548873-
TCGA-AO-A12E-01COSM3825424c.482C>Tp.A161VSubstitution - Missense4:154545846-154545846-
SC_9008COSM3730662c.10-3delTp.?Unknown4:154548938-154548938-
EV001-R9COSM4410586c.392_393insTp.L132fs*6Insertion - Frameshift4:154546134-154546135-
PD4874aCOSM5787835c.475C>Ap.P159TSubstitution - Missense4:154545853-154545853-
I2L-P19Ta-Tumor-OrganoidCOSM4715836c.260-3_260-2insTp.?Unknown4:154547066-154547067-
HDC87COSM4637097c.1251C>Tp.N417NSubstitution - coding silent4:154538009-154538009-
EV001-R2COSM4410586c.392_393insTp.L132fs*6Insertion - Frameshift4:154546134-154546135-
TCGA-FW-A3TU-06COSM3601126c.100C>Tp.P34SSubstitution - Missense4:154548845-154548845-
ZZUFHECRKL-G060TCOSM3760449c.1032A>Gp.Q344QSubstitution - coding silent4:154539961-154539961-
TCGA-FS-A1ZK-06COSM3129168c.1485C>Tp.A495ASubstitution - coding silent4:154537286-154537286-
TCGA-AB-2905-03COSM166743c.1441G>Ap.E481KSubstitution - Missense4:154537330-154537330-
EV001-R4COSM4410586c.392_393insTp.L132fs*6Insertion - Frameshift4:154546134-154546135-
TCGA-D1-A16F-01COSM1052388c.753C>Tp.G251GSubstitution - coding silent4:154540869-154540869-
HCT116COSM3129172c.1081G>Ap.A361TSubstitution - Missense4:154539175-154539175-
Pat_24_BCOSM3129179c.893C>Tp.P298LSubstitution - Missense4:154540640-154540640-
TCGA-FS-A1ZF-06COSM222960c.547C>Tp.P183SSubstitution - Missense4:154544492-154544492-
TCGA-AM-5820-01COSM3760448c.1218T>Ap.I406ISubstitution - coding silent4:154538042-154538042-
TCGA-D3-A2JK-06COSM3601123c.1010G>Ap.R337KSubstitution - Missense4:154539983-154539983-
pfg102TCOSM4763013c.929C>Gp.S310*Substitution - Nonsense4:154540604-154540604-
TCGA-AP-A0LM-01COSM1052383c.1426C>Tp.R476*Substitution - Nonsense4:154537345-154537345-
TCGA-BR-6852-01COSM4122935c.1354G>Ap.A452TSubstitution - Missense4:154537417-154537417-
Au4COSM5604547c.161C>Tp.P54LSubstitution - Missense4:154547809-154547809-
PD9575aCOSM5769664c.260-10G>Tp.?Unknown4:154547074-154547074-
LUAD_E00565COSM389512c.938G>Tp.R313LSubstitution - Missense4:154540595-154540595-
TCGA-B5-A0JY-01COSM1052392c.519G>Tp.K173NSubstitution - Missense4:154544520-154544520-
STC263COSM5060183c.754G>Ap.V252MSubstitution - Missense4:154540868-154540868-
PARBRKCOSM5005549c.222G>Ap.T74TSubstitution - coding silent4:154547748-154547748-
TCGA-AA-A010-01COSM284097c.146G>Ap.R49HSubstitution - Missense4:154547824-154547824-
61COSM5737121c.204G>Tp.K68NSubstitution - Missense4:154547766-154547766-
BD101TCOSM5507364c.1486-8A>Gp.?Unknown4:154536752-154536752-
TCGA-BR-6852-01COSM4122936c.1220A>Tp.Q407LSubstitution - Missense4:154538040-154538040-
001COSM1161888c.391_392insTp.P131fs*7Insertion - Frameshift4:154546135-154546136-
PT08_2COSM5894360c.1485+8C>Tp.?Unknown4:154537278-154537278-
TCGA-43-6143-01COSM732298c.436A>Gp.S146GSubstitution - Missense4:154545892-154545892-
T2932COSM1428101c.543delAp.A182fs*47Deletion - Frameshift4:154544496-154544496-
Pat_32_ACOSM5865929c.1279C>Tp.L427FSubstitution - Missense4:154537981-154537981-
sysucc-880TCOSM5463324c.748C>Tp.R250WSubstitution - Missense4:154540874-154540874-
RK308_C01COSM3767744c.667T>Cp.S223PSubstitution - Missense4:154542207-154542207-
EV001-R5COSM4410586c.392_393insTp.L132fs*6Insertion - Frameshift4:154546134-154546135-
YUZINOCOSM1695124c.208C>Tp.P70SSubstitution - Missense4:154547762-154547762-
TCGA-CM-6171-01COSM3730662c.10-3delTp.?Unknown4:154548938-154548938-
PCSI_0090_Pa_PCOSM3380847c.886T>Cp.L296LSubstitution - coding silent4:154540647-154540647-
TCGA-BR-7196-01COSM4122938c.1021G>Tp.A341SSubstitution - Missense4:154539972-154539972-
SNU-175COSM3129188c.307G>Tp.G103*Substitution - Nonsense4:154547017-154547017-
CN-AML-08-TCOSM3760449c.1032A>Gp.Q344QSubstitution - coding silent4:154539961-154539961-
TCGA-FS-A1ZZ-06COSM1052387c.825C>Tp.L275LSubstitution - coding silent4:154540797-154540797-
TCGA-CG-4305-01COSM4122940c.608A>Gp.H203RSubstitution - Missense4:154542266-154542266-
CSCC-49-TCOSM3601122c.1121C>Tp.S374LSubstitution - Missense4:154539135-154539135-
07-P075COSM4584862c.205G>Cp.G69RSubstitution - Missense4:154547765-154547765-
CSCC-37-TCOSM4461999c.1229C>Tp.S410FSubstitution - Missense4:154538031-154538031-
TCGA-DZ-6133-01COSM3993514c.15A>Gp.V5VSubstitution - coding silent4:154548930-154548930-
TCGA-39-5024-01COSM732297c.404+2T>Ap.?Unknown4:154546121-154546121-
TCGA-B5-A11E-01COSM1052386c.922C>Tp.R308*Substitution - Nonsense4:154540611-154540611-
TCGA-DI-A0WH-01COSM1052391c.606G>Ap.G202GSubstitution - coding silent4:154542268-154542268-
HCC37TCOSM1618507c.1486-9T>Cp.?Unknown4:154536753-154536753-
T3024COSM4715837c.237T>Cp.H79HSubstitution - coding silent4:154547733-154547733-
TCGA-AP-A056-01COSM1052384c.1259C>Tp.T420MSubstitution - Missense4:154538001-154538001-
YURAYCOSM1695123c.536C>Gp.A179GSubstitution - Missense4:154544503-154544503-
TCGA-AZ-4315-01COSM1428100c.894G>Ap.P298PSubstitution - coding silent4:154540639-154540639-
T3090COSM4715835c.412G>Ap.A138TSubstitution - Missense4:154545916-154545916-
TCGA-AP-A0LM-01COSM1052393c.418C>Tp.R140CSubstitution - Missense4:154545910-154545910-
TCGA-A5-A0GP-01COSM1052389c.622C>Tp.R208*Substitution - Nonsense4:154542252-154542252-
BD124TCOSM3730662c.10-3delTp.?Unknown4:154548938-154548938-
TCGA-CG-5721-01COSM4122942c.221C>Tp.T74MSubstitution - Missense4:154547749-154547749-
TCGA-AM-5820-01COSM3760449c.1032A>Gp.Q344QSubstitution - coding silent4:154539961-154539961-
EV001-R1COSM4410586c.392_393insTp.L132fs*6Insertion - Frameshift4:154546134-154546135-
B66-TumorCOSM1753605c.705T>Cp.S235SSubstitution - coding silent4:154540917-154540917-
YUKLABCOSM1695123c.536C>Gp.A179GSubstitution - Missense4:154544503-154544503-
TCGA-FU-A3HZ-01COSM4839799c.844C>Tp.R282WSubstitution - Missense4:154540689-154540689-
TCGA-CF-A1HR-01COSM420154c.1418C>Gp.S473CSubstitution - Missense4:154537353-154537353-
585208COSM326184c.1308G>Tp.M436ISubstitution - Missense4:154537463-154537463-
YUOMEGACOSM5400665c.466C>Tp.R156CSubstitution - Missense4:154545862-154545862-
LOVOCOSM4330288c.14T>Cp.V5ASubstitution - Missense4:154548931-154548931-
CN-AML-NR-08-DxCOSM3760448c.1218T>Ap.I406ISubstitution - coding silent4:154538042-154538042-
I2L-P7-Tumor-OrganoidCOSM3730662c.10-3delTp.?Unknown4:154548938-154548938-
CRC-06TCOSM5457107c.46A>Gp.R16GSubstitution - Missense4:154548899-154548899-
TCGA-BS-A0UF-01COSM1052382c.1520A>Cp.E507ASubstitution - Missense4:154536710-154536710-
TCGA-B5-A0JY-01COSM1052395c.50C>Tp.S17LSubstitution - Missense4:154548895-154548895-
TCGA-HU-8602-01COSM4122934c.1448A>Gp.D483GSubstitution - Missense4:154537323-154537323-
TCGA-18-3409-01COSM732301c.1136T>Cp.V379ASubstitution - Missense4:154539120-154539120-
T47COSM1177583c.25T>Ap.S9TSubstitution - Missense4:154548920-154548920-
TCGA-EE-A2MR-06COSM3601122c.1121C>Tp.S374LSubstitution - Missense4:154539135-154539135-
PT37COSM5918486c.1292-8C>Tp.?Unknown4:154537487-154537487-
PCSI_0090_Pa_XCOSM3380847c.886T>Cp.L296LSubstitution - coding silent4:154540647-154540647-
TCGA-D1-A17Q-01COSM1052394c.125G>Tp.R42LSubstitution - Missense4:154547845-154547845-
TCGA-B5-A11E-01COSM1052389c.622C>Tp.R208*Substitution - Nonsense4:154542252-154542252-
TCGA-FS-A1ZQ-06COSM3601124c.781C>Tp.L261LSubstitution - coding silent4:154540841-154540841-
TCGA-AP-A059-01COSM1052390c.615C>Tp.G205GSubstitution - coding silent4:154542259-154542259-
B66COSM1753605c.705T>Cp.S235SSubstitution - coding silent4:154540917-154540917-
TCGA-AA-3510-01COSM1428102c.145C>Tp.R49CSubstitution - Missense4:154547825-154547825-
TCGA-18-3415-01COSM732303c.1409T>Cp.F470SSubstitution - Missense4:154537362-154537362-
PT23_2COSM1052393c.418C>Tp.R140CSubstitution - Missense4:154545910-154545910-
BK0076COSM4188682c.406delGp.A136fs*27Deletion - Frameshift4:154545922-154545922-
74COSM4777783c.1097_1098insGp.T367fs*10Insertion - Frameshift4:154539158-154539159-
STC252COSM5060182c.1290A>Gp.G430GSubstitution - coding silent4:154537970-154537970-
AML12COSM166743c.1441G>Ap.E481KSubstitution - Missense4:154537330-154537330-
TCGA-46-3769-01COSM732302c.1172C>Gp.S391CSubstitution - Missense4:154538088-154538088-
T17COSM5344651c.529C>Tp.L177LSubstitution - coding silent4:154544510-154544510-
S02375COSM5696617c.902A>Cp.D301ASubstitution - Missense4:154540631-154540631-
TCGA-B0-5703-01COSM480979c.628A>Gp.I210VSubstitution - Missense4:154542246-154542246-
S00825COSM5701078c.10-3_10-2insTp.?Unknown4:154548937-154548938-
TCGA-DI-A0WH-01COSM1052385c.970C>Tp.H324YSubstitution - Missense4:154540023-154540023-
TCGA-BR-4184-01COSM4122937c.1130C>Ap.A377DSubstitution - Missense4:154539126-154539126-
RDESCOSM4584861c.1230C>Tp.S410SSubstitution - coding silent4:154538030-154538030-
EV001-R8COSM4410586c.392_393insTp.L132fs*6Insertion - Frameshift4:154546134-154546135-
ESCC_55COSM5631998c.288T>Gp.G96GSubstitution - coding silent4:154547036-154547036-
CSCC-49-TCOSM4571511c.477T>Ap.P159PSubstitution - coding silent4:154545851-154545851-
TCGA-A4-7584-01COSM3993513c.543A>Gp.K181KSubstitution - coding silent4:154544496-154544496-
sysucc-880TCOSM1052391c.606G>Ap.G202GSubstitution - coding silent4:154542268-154542268-
EV001-R3COSM4410586c.392_393insTp.L132fs*6Insertion - Frameshift4:154546134-154546135-
T263COSM4715836c.260-3_260-2insTp.?Unknown4:154547066-154547067-
234COSM3730662c.10-3delTp.?Unknown4:154548938-154548938-
CN-AML-NR-08-DxCOSM3760449c.1032A>Gp.Q344QSubstitution - coding silent4:154539961-154539961-
TCGA-BR-8487-01COSM4122941c.445C>Ap.R149RSubstitution - coding silent4:154545883-154545883-
LUAD-B01811COSM334579c.555G>Tp.M185ISubstitution - Missense4:154544484-154544484-
SNU-C4COSM3129170c.1238A>Cp.N413TSubstitution - Missense4:154538022-154538022-
ME009TCOSM222960c.547C>Tp.P183SSubstitution - Missense4:154544492-154544492-
TCGA-21-1077-01COSM732299c.894G>Tp.P298PSubstitution - coding silent4:154540639-154540639-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.2499964q31.2-q32.1605961
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGIntronicSNV.c.404+47T>C4155467228CM
AGMissensep.F470Sc.1409T>C4155458514LUSC
AGMissensep.V375Ac.1124T>C4155460284MM
ATSpliceDonorSNV.c.404+2T>A4155467273LUSC
CAMissensep.M436Ic.1308G>T4155458615SCLC
CASynonymousp.P298Pc.894G>T4155461791LUSC
CCTT5-UTRBlockSubstitution.c.1-82_1-81delinsAA4155471541CM
CTIntronicSNV.c.940-63G>A4155461268CM
CTMissensep.A452Tc.1354G>A4155458569STAD
CTMissensep.E481Kc.1441G>A4155458482AML
CTMissensep.G105Ec.314G>A4155467365CM
CTMissensep.R337Kc.1010G>A4155461135CM
CTNonsensep.W439*c.1317G>A4155458606CM
CTSynonymousp.G202Gc.606G>A4155463420UCEC
CTSynonymousp.L177Lc.531G>A4155465660CM
GAIntronicSNV.c.1151+14C>T4155460243CM
GAIntronicSNV.c.404+72C>T4155467203CM
GAMissensep.H324Yc.970C>T4155461175UCEC
GAMissensep.P183Sc.547C>T4155465644CM
GAMissensep.T134Ic.401C>T4155467278CM
GANonsensep.R208*c.622C>T4155463404UCEC
GASynonymousp.A495Ac.1485C>T4155458438CM
GASynonymousp.G251Gc.753C>T4155462021UCEC
GASynonymousp.L261Lc.781C>T4155461993CM
GASynonymousp.L275Lc.825C>T4155461949CM
GASynonymousp.S410Sc.1230C>T4155459182LGG
GCMissensep.S391Cc.1172C>G4155459240LUSC
GCMissensep.S473Cc.1418C>G4155458505BLCA
GCMissensep.T369Rc.1106C>G4155460302CM
TAMissensep.Q407Lc.1220A>T4155459192STAD
TAMissensep.S119Cc.355A>T4155467324CM
TCMissensep.H203Rc.608A>G4155463418STAD
TCMissensep.H40Rc.119A>G4155469003STAD
TCMissensep.I416Vc.1246A>G4155459166HNSC
TCMissensep.S146Gc.436A>G4155467044LUSC