FBXW2
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA9123526953123526953+Missense_MutationSNPCCTTCGA-DK-A6B1-01A-12D-A30E-08TCGA-DK-A6B1-10A-01D-A30H-08g.chr9:123526953C>Tc.1249G>Ac.(1249-1251)Gca>Acap.A417T
BLCA9123526972123526972+Missense_MutationSNPCCGTCGA-FD-A43P-01A-31D-A23U-08TCGA-FD-A43P-10A-01D-A23U-08g.chr9:123526972C>Gc.1230G>Cc.(1228-1230)aaG>aaCp.K410N
BLCA9123527035123527035+SilentSNPGGATCGA-FD-A6TC-01A-21D-A339-08TCGA-FD-A6TC-10A-21D-A339-08g.chr9:123527035G>Ac.1167C>Tc.(1165-1167)atC>atTp.I389I
BLCA9123540762123540762+SilentSNPGGATCGA-XF-AAN0-01A-11D-A42E-08TCGA-XF-AAN0-10A-01D-A42H-08g.chr9:123540762G>Ac.552C>Tc.(550-552)atC>atTp.I184I
BLCA9123550224123550224+Missense_MutationSNPAACTCGA-DK-A6AW-01A-11D-A30E-08TCGA-DK-A6AW-10A-01D-A30H-08g.chr9:123550224A>Cc.313T>Gc.(313-315)Ttg>Gtgp.L105V
BLCA9123550366123550366+SilentSNPGGCTCGA-BT-A3PH-01A-11D-A21Z-08TCGA-BT-A3PH-10A-01D-A21Z-08g.chr9:123550366G>Cc.171C>Gc.(169-171)ctC>ctGp.L57L
BLCA9123550458123550458+Missense_MutationSNPCCTTCGA-DK-AA6Q-01A-11D-A391-08TCGA-DK-AA6Q-10A-01D-A394-08g.chr9:123550458C>Tc.79G>Ac.(79-81)Gaa>Aaap.E27K
BLCA9123550531123550531+Missense_MutationSNPCCGTCGA-DK-AA6Q-01A-11D-A391-08TCGA-DK-AA6Q-10A-01D-A394-08g.chr9:123550531C>Gc.6G>Cc.(4-6)gaG>gaCp.E2D
BRCA9123526846123526846+SilentSNPCCTTCGA-BH-A0HF-01A-11W-A071-09TCGA-BH-A0HF-10A-01W-A071-09g.chr9:123526846C>Tc.1356G>Ac.(1354-1356)gaG>gaAp.E452E
BRCA9123527011123527011+SilentSNPCCGTCGA-AC-A23H-01A-11D-A159-09TCGA-AC-A23H-11A-12D-A17G-09g.chr9:123527011C>Gc.1191G>Cc.(1189-1191)ctG>ctCp.L397L
BRCA9123527031123527031+Missense_MutationSNPCCTTCGA-D8-A27G-01A-11D-A16D-09TCGA-D8-A27G-10A-01D-A16D-09g.chr9:123527031C>Tc.1171G>Ac.(1171-1173)Gac>Aacp.D391N
BRCA9123533674123533674+Missense_MutationSNPGGATCGA-A2-A0EY-01A-11W-A050-09TCGA-A2-A0EY-10A-01W-A055-09g.chr9:123533674G>Ac.1028C>Tc.(1027-1029)tCa>tTap.S343L
BRCA9123535049123535049+Missense_MutationSNPCCTTCGA-D8-A27G-01A-11D-A16D-09TCGA-D8-A27G-10A-01D-A16D-09g.chr9:123535049C>Tc.889G>Ac.(889-891)Gac>Aacp.D297N
BRCA9123550286123550286+Missense_MutationSNPGGCTCGA-E2-A15M-01A-11D-A12B-09TCGA-E2-A15M-11A-22D-A12B-09g.chr9:123550286G>Cc.251C>Gc.(250-252)tCt>tGtp.S84C
CESC9123533705123533705+Missense_MutationSNPGGATCGA-DR-A0ZM-01A-12D-A10S-08TCGA-DR-A0ZM-10A-01D-A10S-08g.chr9:123533705G>Ac.997C>Tc.(997-999)Cat>Tatp.H333Y
CESC9123540630123540630+Splice_SiteSNPCCTTCGA-EK-A2PI-01A-11D-A18J-09TCGA-EK-A2PI-10A-01D-A18J-09g.chr9:123540630C>Tc.684G>Ac.(682-684)gcG>gcAp.A228A
CHOL9123550286123550286+Missense_MutationSNPGGTTCGA-4G-AAZO-01A-12D-A417-09TCGA-4G-AAZO-11A-11D-A41A-09g.chr9:123550286G>Tc.251C>Ac.(250-252)tCt>tAtp.S84Y
COAD9123527004123527004+Missense_MutationSNPGGATCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr9:123527004G>Ac.1198C>Tc.(1198-1200)Cgc>Tgcp.R400C
COAD9123538407123538407+SilentSNPCCATCGA-A6-5661-01A-01D-1650-10TCGA-A6-5661-10A-01D-1650-10g.chr9:123538407C>Ac.783G>Tc.(781-783)ctG>ctTp.L261L
COAD9123538408123538408+Missense_MutationSNPAAGTCGA-D5-6533-01A-11D-1719-10TCGA-D5-6533-10A-01D-1719-10g.chr9:123538408A>Gc.782T>Cc.(781-783)cTg>cCgp.L261P
COAD9123538451123538451+Missense_MutationSNPCCATCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr9:123538451C>Ac.739G>Tc.(739-741)Gac>Tacp.D247Y
COAD9123550475123550475+Missense_MutationSNPGGATCGA-CM-4743-01A-01D-1719-10TCGA-CM-4743-10A-01D-1719-10g.chr9:123550475G>Ac.62C>Tc.(61-63)aCg>aTgp.T21M
COAD9123550529123550529+Missense_MutationSNPCCATCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr9:123550529C>Ac.8G>Tc.(7-9)aGa>aTap.R3I
COADREAD9123527004123527004+Missense_MutationSNPGGATCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr9:123527004G>Ac.1198C>Tc.(1198-1200)Cgc>Tgcp.R400C
COADREAD9123538407123538407+SilentSNPCCATCGA-A6-5661-01A-01D-1650-10TCGA-A6-5661-10A-01D-1650-10g.chr9:123538407C>Ac.783G>Tc.(781-783)ctG>ctTp.L261L
COADREAD9123538408123538408+Missense_MutationSNPAAGTCGA-D5-6533-01A-11D-1719-10TCGA-D5-6533-10A-01D-1719-10g.chr9:123538408A>Gc.782T>Cc.(781-783)cTg>cCgp.L261P
COADREAD9123538451123538451+Missense_MutationSNPCCATCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr9:123538451C>Ac.739G>Tc.(739-741)Gac>Tacp.D247Y
COADREAD9123550147123550147+Missense_MutationSNPCCATCGA-AG-3892-01A-01W-1073-09TCGA-AG-3892-10A-01W-1073-09g.chr9:123550147C>Ac.390G>Tc.(388-390)atG>atTp.M130I
COADREAD9123550475123550475+Missense_MutationSNPGGATCGA-CM-4743-01A-01D-1719-10TCGA-CM-4743-10A-01D-1719-10g.chr9:123550475G>Ac.62C>Tc.(61-63)aCg>aTgp.T21M
COADREAD9123550529123550529+Missense_MutationSNPCCATCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr9:123550529C>Ac.8G>Tc.(7-9)aGa>aTap.R3I
ESCA9123527004123527004+Missense_MutationSNPGGTTCGA-L5-A4OJ-01A-11D-A27G-09TCGA-L5-A4OJ-11A-12D-A27G-09g.chr9:123527004G>Tc.1198C>Ac.(1198-1200)Cgc>Agcp.R400S
ESCA9123538400123538400+Missense_MutationSNPGGTTCGA-LN-A8I1-01A-11D-A36J-09TCGA-LN-A8I1-10A-01D-A36M-09g.chr9:123538400G>Tc.790C>Ac.(790-792)Ctc>Atcp.L264I
ESCA9123550234123550234+SilentSNPTTCTCGA-L5-A8NM-01A-11D-A37C-09TCGA-L5-A8NM-11A-12D-A37F-09g.chr9:123550234T>Cc.303A>Gc.(301-303)gcA>gcGp.A101A
HNSC9123538450123538450+Missense_MutationSNPTTATCGA-IQ-A61L-01A-11D-A30E-08TCGA-IQ-A61L-10A-01D-A30H-08g.chr9:123538450T>Ac.740A>Tc.(739-741)gAc>gTcp.D247V
HNSC9123540631123540631+Missense_MutationSNPGGATCGA-HD-A633-01A-11D-A28R-08TCGA-HD-A633-10A-01D-A28U-08g.chr9:123540631G>Ac.683C>Tc.(682-684)gCg>gTgp.A228V
HNSC9123550177123550177+SilentSNPCCTTCGA-CR-7398-01A-11D-2012-08TCGA-CR-7398-10A-01D-2013-08g.chr9:123550177C>Tc.360G>Ac.(358-360)aaG>aaAp.K120K
KIPAN9123527053123527053+SilentSNPGGATCGA-A4-8312-01A-11D-2396-08TCGA-A4-8312-10A-01D-2396-08g.chr9:123527053G>Ac.1149C>Tc.(1147-1149)gaC>gaTp.D383D
KIPAN9123533652123533652+Missense_MutationSNPCCGTCGA-2Z-A9JE-01A-11D-A42J-10TCGA-2Z-A9JE-10A-01D-A42M-10g.chr9:123533652C>Gc.1050G>Cc.(1048-1050)tgG>tgCp.W350C
KIRP9123527053123527053+SilentSNPGGATCGA-A4-8312-01A-11D-2396-08TCGA-A4-8312-10A-01D-2396-08g.chr9:123527053G>Ac.1149C>Tc.(1147-1149)gaC>gaTp.D383D
KIRP9123533652123533652+Missense_MutationSNPCCGTCGA-2Z-A9JE-01A-11D-A42J-10TCGA-2Z-A9JE-10A-01D-A42M-10g.chr9:123533652C>Gc.1050G>Cc.(1048-1050)tgG>tgCp.W350C
LIHC9123526906123526906+SilentSNPCCTTCGA-DD-A3A9-01A-11D-A25V-10TCGA-DD-A3A9-11A-11D-A25V-10g.chr9:123526906C>Tc.1296G>Ac.(1294-1296)acG>acAp.T432T
LIHC9123526947123526947+Missense_MutationSNPCCTTCGA-EP-A2KA-01A-11D-A183-10TCGA-EP-A2KA-10A-01D-A183-10g.chr9:123526947C>Tc.1255G>Ac.(1255-1257)Gaa>Aaap.E419K
LIHC9123526956123526956+Missense_MutationSNPGGTTCGA-EP-A2KA-01A-11D-A183-10TCGA-EP-A2KA-10A-01D-A183-10g.chr9:123526956G>Tc.1246C>Ac.(1246-1248)Ctg>Atgp.L416M
LIHC9123533666123533666+Missense_MutationSNPCCTTCGA-4R-AA8I-01A-11D-A382-10TCGA-4R-AA8I-10B-01D-A385-10g.chr9:123533666C>Tc.1036G>Ac.(1036-1038)Ggt>Agtp.G346S
LUAD9123535119123535119+Splice_SiteSNPCCATCGA-64-5781-01A-01D-1625-08TCGA-64-5781-10A-01D-1625-08g.chr9:123535119C>Ac.e6-1
LUAD9123538385123538385+Missense_MutationSNPCCTTCGA-86-A4JF-01A-11D-A24P-08TCGA-86-A4JF-10A-01D-A24P-08g.chr9:123538385C>Tc.805G>Ac.(805-807)Gaa>Aaap.E269K
LUAD9123538418123538418+Missense_MutationSNPCCATCGA-55-7994-01A-11D-2184-08TCGA-55-7994-10A-01D-2184-08g.chr9:123538418C>Ac.772G>Tc.(772-774)Ggg>Tggp.G258W
LUAD9123550109123550109+Nonsense_MutationSNPGGCTCGA-17-Z031-01A-01W-0746-08TCGA-17-Z031-11A-01W-0746-08g.chr9:123550109G>Cc.428C>Gc.(427-429)tCa>tGap.S143*
OV9123538409123538409+Missense_MutationSNPGGCTCGA-04-1530-01A-02W-0552-10TCGA-04-1530-10A-01W-0552-10g.chr9:123538409G>Cc.781C>Gc.(781-783)Ctg>Gtgp.L261V
PAAD9123527025123527025+Missense_MutationSNPGGATCGA-HV-A7OL-01A-11D-A33T-08TCGA-HV-A7OL-10A-01D-A33W-08g.chr9:123527025G>Ac.1177C>Tc.(1177-1179)Cgg>Tggp.R393W
PAAD9123527025123527025+Missense_MutationSNPGGATCGA-US-A77J-01A-11D-A32N-08TCGA-US-A77J-11A-11D-A32N-08g.chr9:123527025G>Ac.1177C>Tc.(1177-1179)Cgg>Tggp.R393W
PAAD9123538497123538497+SilentSNPGGATCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr9:123538497G>Ac.693C>Tc.(691-693)agC>agTp.S231S
PCPG9123550425123550425+Missense_MutationSNPCCTTCGA-RW-A68A-01A-11D-A35D-08TCGA-RW-A68A-11A-21D-A35B-08g.chr9:123550425C>Tc.112G>Ac.(112-114)Gca>Acap.A38T
READ9123550147123550147+Missense_MutationSNPCCATCGA-AG-3892-01A-01W-1073-09TCGA-AG-3892-10A-01W-1073-09g.chr9:123550147C>Ac.390G>Tc.(388-390)atG>atTp.M130I
SKCM9123550194123550194+Missense_MutationSNPCCTTCGA-D3-A2JF-06A-11D-A196-08TCGA-D3-A2JF-10A-01D-A198-08g.chr9:123550194C>Tc.343G>Ac.(343-345)Gac>Aacp.D115N
SKCM9123550195123550195+SilentSNPCCTTCGA-D3-A2JF-06A-11D-A196-08TCGA-D3-A2JF-10A-01D-A198-08g.chr9:123550195C>Tc.342G>Ac.(340-342)caG>caAp.Q114Q
SKCM9123550268123550268+Missense_MutationSNPAACTCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr9:123550268A>Cc.269T>Gc.(268-270)gTg>gGgp.V90G
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-US9123550366123550366single base substitutionGC5_prime_UTR_premature_start_codon_gain_variant
BLCA-US9123550366123550366single base substitutionGCexon_variant
BLCA-US9123550366123550366single base substitutionGCsynonymous_variantL57L171C>G
BRCA-EU9123509720123509720single base substitutionGAdownstream_gene_variant
BRCA-EU9123510710123510710single base substitutionCTdownstream_gene_variant
BRCA-EU9123512591123512591single base substitutionCTdownstream_gene_variant
BRCA-EU9123513617123513617single base substitutionACdownstream_gene_variant
BRCA-EU9123515531123515532deletion of <=200bpTG-downstream_gene_variant
BRCA-EU9123515531123515532deletion of <=200bpTG-exon_variant
BRCA-EU9123516541123516541single base substitutionGCdownstream_gene_variant
BRCA-EU9123516541123516541single base substitutionGCintron_variant
BRCA-EU9123517301123517301single base substitutionCGdownstream_gene_variant
BRCA-EU9123517301123517301single base substitutionCGintron_variant
BRCA-EU9123517387123517387single base substitutionCGdownstream_gene_variant
BRCA-EU9123517387123517387single base substitutionCGintron_variant
BRCA-EU9123517589123517589deletion of <=200bpT-downstream_gene_variant
BRCA-EU9123517589123517589deletion of <=200bpT-intron_variant
BRCA-EU9123518326123518326single base substitutionTAdownstream_gene_variant
BRCA-EU9123518326123518326single base substitutionTAintron_variant
BRCA-EU9123521131123521131single base substitutionCA3_prime_UTR_variant
BRCA-EU9123521131123521131single base substitutionCAintron_variant
BRCA-EU9123523664123523664single base substitutionTA3_prime_UTR_variant
BRCA-EU9123523664123523664single base substitutionTAdownstream_gene_variant
BRCA-EU9123523664123523664single base substitutionTAintron_variant
BRCA-EU9123523690123523690single base substitutionCT3_prime_UTR_variant
BRCA-EU9123523690123523690single base substitutionCTdownstream_gene_variant
BRCA-EU9123523690123523690single base substitutionCTintron_variant
BRCA-EU9123526197123526197single base substitutionCG3_prime_UTR_variant
BRCA-EU9123526197123526197single base substitutionCGdownstream_gene_variant
BRCA-EU9123526197123526197single base substitutionCGintron_variant
BRCA-EU9123526358123526358single base substitutionCG3_prime_UTR_variant
BRCA-EU9123526358123526358single base substitutionCGdownstream_gene_variant
BRCA-EU9123526358123526358single base substitutionCGintron_variant
BRCA-EU9123527480123527480single base substitutionCTintron_variant
BRCA-EU9123527545123527545single base substitutionGAintron_variant
BRCA-EU9123527601123527601single base substitutionGAintron_variant
BRCA-EU9123530806123530806single base substitutionTAdownstream_gene_variant
BRCA-EU9123530806123530806single base substitutionTAintron_variant
BRCA-EU9123531616123531616single base substitutionCAdownstream_gene_variant
BRCA-EU9123531616123531616single base substitutionCAintron_variant
BRCA-EU9123531918123531918insertion of <=200bp-Adownstream_gene_variant
BRCA-EU9123531918123531918insertion of <=200bp-Aintron_variant
BRCA-EU9123532054123532054single base substitutionGAdownstream_gene_variant
BRCA-EU9123532054123532054single base substitutionGAintron_variant
BRCA-EU9123534975123534977deletion of <=200bpTTC-downstream_gene_variant
BRCA-EU9123534975123534977deletion of <=200bpTTC-intron_variant
BRCA-EU9123536895123536895single base substitutionTCdownstream_gene_variant
BRCA-EU9123536895123536895single base substitutionTCintron_variant
BRCA-EU9123539868123539868single base substitutionCTintron_variant
BRCA-EU9123539868123539868single base substitutionCTupstream_gene_variant
BRCA-EU9123540001123540001insertion of <=200bp-Aintron_variant
BRCA-EU9123540001123540001insertion of <=200bp-Aupstream_gene_variant
BRCA-EU9123543178123543178single base substitutionGAintron_variant
BRCA-EU9123543178123543178single base substitutionGAupstream_gene_variant
BRCA-EU9123545457123545458deletion of <=200bpAA-downstream_gene_variant
BRCA-EU9123545457123545458deletion of <=200bpAA-intron_variant
BRCA-EU9123548758123548758single base substitutionGAdownstream_gene_variant
BRCA-EU9123548758123548758single base substitutionGAintron_variant
BRCA-EU9123549463123549463single base substitutionCTdownstream_gene_variant
BRCA-EU9123549463123549463single base substitutionCTintron_variant
BRCA-EU9123550246123550246single base substitutionCT5_prime_UTR_premature_start_codon_gain_variant
BRCA-EU9123550246123550246single base substitutionCTdownstream_gene_variant
BRCA-EU9123550246123550246single base substitutionCTexon_variant
BRCA-EU9123550246123550246single base substitutionCTsynonymous_variantV97V291G>A
BRCA-EU9123551230123551230single base substitutionGCintron_variant
BRCA-EU9123555819123555819single base substitutionCTupstream_gene_variant
BRCA-EU9123557136123557136single base substitutionGAupstream_gene_variant
BRCA-EU9123557335123557335single base substitutionGCupstream_gene_variant
BRCA-EU9123557792123557792single base substitutionGCupstream_gene_variant
BRCA-EU9123557833123557833single base substitutionGAupstream_gene_variant
BRCA-EU9123558010123558010single base substitutionGTupstream_gene_variant
BRCA-FR9123517301123517301single base substitutionCGdownstream_gene_variant
BRCA-FR9123517301123517301single base substitutionCGintron_variant
BRCA-FR9123521131123521131single base substitutionCA3_prime_UTR_variant
BRCA-FR9123521131123521131single base substitutionCAintron_variant
BRCA-FR9123527480123527480single base substitutionCTintron_variant
BRCA-FR9123543583123543583single base substitutionGAintron_variant
BRCA-FR9123543583123543583single base substitutionGAupstream_gene_variant
BRCA-FR9123551230123551230single base substitutionGCintron_variant
BRCA-FR9123555819123555819single base substitutionCTupstream_gene_variant
BRCA-UK9123518326123518326single base substitutionTAdownstream_gene_variant
BRCA-UK9123518326123518326single base substitutionTAintron_variant
BRCA-US9123526846123526846single base substitutionCTintron_variant
BRCA-US9123526846123526846single base substitutionCTsynonymous_variantE387E1161G>A
BRCA-US9123526846123526846single base substitutionCTsynonymous_variantE452E1356G>A
BRCA-US9123527011123527011single base substitutionCGintron_variant
BRCA-US9123527011123527011single base substitutionCGsynonymous_variantL332L996G>C
BRCA-US9123527011123527011single base substitutionCGsynonymous_variantL397L1191G>C
BRCA-US9123527031123527031single base substitutionCTintron_variant
BRCA-US9123527031123527031single base substitutionCTmissense_variantD326N976G>A
BRCA-US9123527031123527031single base substitutionCTmissense_variantD391N1171G>A
BRCA-US9123533674123533674single base substitutionGAdownstream_gene_variant
BRCA-US9123533674123533674single base substitutionGAexon_variant
BRCA-US9123533674123533674single base substitutionGAmissense_variantS278L833C>T
BRCA-US9123533674123533674single base substitutionGAmissense_variantS343L1028C>T
BRCA-US9123535049123535049single base substitutionCTdownstream_gene_variant
BRCA-US9123535049123535049single base substitutionCTexon_variant
BRCA-US9123535049123535049single base substitutionCTmissense_variantD168N502G>A
BRCA-US9123535049123535049single base substitutionCTmissense_variantD232N694G>A
BRCA-US9123535049123535049single base substitutionCTmissense_variantD297N889G>A
BRCA-US9123550286123550286single base substitutionGC5_prime_UTR_premature_start_codon_gain_variant
BRCA-US9123550286123550286single base substitutionGCdownstream_gene_variant
BRCA-US9123550286123550286single base substitutionGCexon_variant
BRCA-US9123550286123550286single base substitutionGCmissense_variantS84C251C>G
BTCA-JP9123533794123533794single base substitutionATdownstream_gene_variant
BTCA-JP9123533794123533794single base substitutionATmissense_variantI174N521T>A
BTCA-JP9123533794123533794single base substitutionATmissense_variantI238N713T>A
BTCA-JP9123533794123533794single base substitutionATmissense_variantI303N908T>A
BTCA-JP9123533794123533794single base substitutionATsplice_region_variant
CESC-US9123533705123533705single base substitutionGAdownstream_gene_variant
CESC-US9123533705123533705single base substitutionGAexon_variant
CESC-US9123533705123533705single base substitutionGAmissense_variantH204Y610C>T
CESC-US9123533705123533705single base substitutionGAmissense_variantH268Y802C>T
CESC-US9123533705123533705single base substitutionGAmissense_variantH333Y997C>T
CESC-US9123540630123540630single base substitutionCTintron_variant
CESC-US9123540630123540630single base substitutionCTsplice_region_variant
CESC-US9123540630123540630single base substitutionCTupstream_gene_variant
CESC-US9123555327123555327single base substitutionCTexon_variant
CESC-US9123555327123555327single base substitutionCTintron_variant
COAD-US9123527004123527004single base substitutionGAintron_variant
COAD-US9123527004123527004single base substitutionGAmissense_variantR335C1003C>T
COAD-US9123527004123527004single base substitutionGAmissense_variantR400C1198C>T
COAD-US9123550191123550191single base substitutionCT5_prime_UTR_variant
COAD-US9123550191123550191single base substitutionCTdownstream_gene_variant
COAD-US9123550191123550191single base substitutionCTexon_variant
COAD-US9123550191123550191single base substitutionCTmissense_variantA116T346G>A
COAD-US9123550475123550475single base substitutionGAexon_variant
COAD-US9123550475123550475single base substitutionGAintron_variant
COAD-US9123550475123550475single base substitutionGAmissense_variantT21M62C>T
COCA-CN9123515325123515325single base substitutionTCdownstream_gene_variant
COCA-CN9123515325123515325single base substitutionTCexon_variant
COCA-CN9123540866123540866single base substitutionCTintron_variant
COCA-CN9123540866123540866single base substitutionCTupstream_gene_variant
EOPC-DE9123537490123537490single base substitutionTAdownstream_gene_variant
EOPC-DE9123537490123537490single base substitutionTAintron_variant
ESAD-UK9123510464123510464single base substitutionTCdownstream_gene_variant
ESAD-UK9123510764123510764single base substitutionCTdownstream_gene_variant
ESAD-UK9123511074123511081deletion of <=200bpCTTATCTC-downstream_gene_variant
ESAD-UK9123512470123512470single base substitutionGAdownstream_gene_variant
ESAD-UK9123513124123513124single base substitutionGCdownstream_gene_variant
ESAD-UK9123513819123513819single base substitutionGAdownstream_gene_variant
ESAD-UK9123514109123514109single base substitutionGTdownstream_gene_variant
ESAD-UK9123516014123516014deletion of <=200bpA-downstream_gene_variant
ESAD-UK9123516014123516014deletion of <=200bpA-intron_variant
ESAD-UK9123517018123517018single base substitutionTAdownstream_gene_variant
ESAD-UK9123517018123517018single base substitutionTAintron_variant
ESAD-UK9123517432123517432single base substitutionTCdownstream_gene_variant
ESAD-UK9123517432123517432single base substitutionTCintron_variant
ESAD-UK9123518282123518282single base substitutionTGdownstream_gene_variant
ESAD-UK9123518282123518282single base substitutionTGintron_variant
ESAD-UK9123521121123521121single base substitutionAG3_prime_UTR_variant
ESAD-UK9123521121123521121single base substitutionAGintron_variant
ESAD-UK9123527429123527429single base substitutionGAintron_variant
ESAD-UK9123529037123529037single base substitutionGTdownstream_gene_variant
ESAD-UK9123529037123529037single base substitutionGTintron_variant
ESAD-UK9123530601123530601single base substitutionATdownstream_gene_variant
ESAD-UK9123530601123530601single base substitutionATintron_variant
ESAD-UK9123536342123536342single base substitutionGAdownstream_gene_variant
ESAD-UK9123536342123536342single base substitutionGAintron_variant
ESAD-UK9123537027123537027single base substitutionCTdownstream_gene_variant
ESAD-UK9123537027123537027single base substitutionCTintron_variant
ESAD-UK9123537884123537884single base substitutionTAdownstream_gene_variant
ESAD-UK9123537884123537884single base substitutionTAintron_variant
ESAD-UK9123540268123540268single base substitutionGAintron_variant
ESAD-UK9123540268123540268single base substitutionGAupstream_gene_variant
ESAD-UK9123540728123540728single base substitutionCGexon_variant
ESAD-UK9123540728123540728single base substitutionCGintron_variant
ESAD-UK9123540728123540728single base substitutionCGmissense_variantE196Q586G>C
ESAD-UK9123540728123540728single base substitutionCGmissense_variantE67Q199G>C
ESAD-UK9123540728123540728single base substitutionCGupstream_gene_variant
ESAD-UK9123545695123545695deletion of <=200bpA-downstream_gene_variant
ESAD-UK9123545695123545695deletion of <=200bpA-intron_variant
ESAD-UK9123546499123546499single base substitutionATdownstream_gene_variant
ESAD-UK9123546499123546499single base substitutionATintron_variant
ESAD-UK9123549169123549169single base substitutionTCdownstream_gene_variant
ESAD-UK9123549169123549169single base substitutionTCintron_variant
ESAD-UK9123549283123549283single base substitutionGAdownstream_gene_variant
ESAD-UK9123549283123549283single base substitutionGAintron_variant
ESAD-UK9123556502123556502single base substitutionGAupstream_gene_variant
ESAD-UK9123559163123559163single base substitutionCTupstream_gene_variant
ESCA-CN9123540741123540741single base substitutionCTexon_variant
ESCA-CN9123540741123540741single base substitutionCTintron_variant
ESCA-CN9123540741123540741single base substitutionCTsynonymous_variantA191A573G>A
ESCA-CN9123540741123540741single base substitutionCTsynonymous_variantA62A186G>A
ESCA-CN9123540741123540741single base substitutionCTupstream_gene_variant
ESCA-CN9123540764123540764single base substitutionTCexon_variant
ESCA-CN9123540764123540764single base substitutionTCintron_variant
ESCA-CN9123540764123540764single base substitutionTCmissense_variantI184V550A>G
ESCA-CN9123540764123540764single base substitutionTCmissense_variantI55V163A>G
ESCA-CN9123540764123540764single base substitutionTCupstream_gene_variant
KIRP-US9123527053123527053single base substitutionGAintron_variant
KIRP-US9123527053123527053single base substitutionGAsynonymous_variantD318D954C>T
KIRP-US9123527053123527053single base substitutionGAsynonymous_variantD383D1149C>T
LAML-KR9123524671123524671single base substitutionCT3_prime_UTR_variant
LAML-KR9123524671123524671single base substitutionCTdownstream_gene_variant
LAML-KR9123524671123524671single base substitutionCTintron_variant
LICA-FR9123512530123512530deletion of <=200bpT-downstream_gene_variant
LICA-FR9123512530123512530insertion of <=200bp-Tdownstream_gene_variant
LICA-FR9123512530123512531deletion of <=200bpTT-downstream_gene_variant
LICA-FR9123526843123526843single base substitutionGAintron_variant
LICA-FR9123526843123526843single base substitutionGAsynonymous_variantH388H1164C>T
LICA-FR9123526843123526843single base substitutionGAsynonymous_variantH453H1359C>T
LICA-FR9123537213123537213single base substitutionGTdownstream_gene_variant
LICA-FR9123537213123537213single base substitutionGTintron_variant
LICA-FR9123543957123543957single base substitutionCTintron_variant
LICA-FR9123545399123545399single base substitutionCAdownstream_gene_variant
LICA-FR9123545399123545399single base substitutionCAintron_variant
LIHC-US9123526906123526906single base substitutionCTintron_variant
LIHC-US9123526906123526906single base substitutionCTsynonymous_variantT367T1101G>A
LIHC-US9123526906123526906single base substitutionCTsynonymous_variantT432T1296G>A
LIHC-US9123526947123526947single base substitutionCTintron_variant
LIHC-US9123526947123526947single base substitutionCTmissense_variantE354K1060G>A
LIHC-US9123526947123526947single base substitutionCTmissense_variantE419K1255G>A
LINC-JP9123532522123532522single base substitutionCTdownstream_gene_variant
LINC-JP9123532522123532522single base substitutionCTintron_variant
LINC-JP9123535140123535140single base substitutionCAdownstream_gene_variant
LINC-JP9123535140123535140single base substitutionCAintron_variant
LINC-JP9123538720123538720single base substitutionCTexon_variant
LINC-JP9123538720123538720single base substitutionCTintron_variant
LINC-JP9123543913123543913single base substitutionTCintron_variant
LINC-JP9123543913123543913single base substitutionTCupstream_gene_variant
LINC-JP9123554282123554282single base substitutionTCintron_variant
LINC-JP9123555306123555306single base substitutionACexon_variant
LINC-JP9123555306123555306single base substitutionACintron_variant
LIRI-JP9123509716123509716single base substitutionCTdownstream_gene_variant
LIRI-JP9123512504123512504single base substitutionTCdownstream_gene_variant
LIRI-JP9123514004123514004single base substitutionTCdownstream_gene_variant
LIRI-JP9123516406123516406single base substitutionTCdownstream_gene_variant
LIRI-JP9123516406123516406single base substitutionTCintron_variant
LIRI-JP9123523332123523332single base substitutionTC3_prime_UTR_variant
LIRI-JP9123523332123523332single base substitutionTCdownstream_gene_variant
LIRI-JP9123523332123523332single base substitutionTCintron_variant
LIRI-JP9123524003123524003single base substitutionTC3_prime_UTR_variant
LIRI-JP9123524003123524003single base substitutionTCdownstream_gene_variant
LIRI-JP9123524003123524003single base substitutionTCintron_variant
LIRI-JP9123525059123525059single base substitutionGT3_prime_UTR_variant
LIRI-JP9123525059123525059single base substitutionGTdownstream_gene_variant
LIRI-JP9123525059123525059single base substitutionGTintron_variant
LIRI-JP9123526948123526948single base substitutionGAintron_variant
LIRI-JP9123526948123526948single base substitutionGAsynonymous_variantG353G1059C>T
LIRI-JP9123526948123526948single base substitutionGAsynonymous_variantG418G1254C>T
LIRI-JP9123528611123528611single base substitutionACintron_variant
LIRI-JP9123529177123529177single base substitutionCTdownstream_gene_variant
LIRI-JP9123529177123529177single base substitutionCTintron_variant
LIRI-JP9123529259123529259single base substitutionCAdownstream_gene_variant
LIRI-JP9123529259123529259single base substitutionCAintron_variant
LIRI-JP9123529276123529276single base substitutionTCdownstream_gene_variant
LIRI-JP9123529276123529276single base substitutionTCintron_variant
LIRI-JP9123533380123533380single base substitutionGAdownstream_gene_variant
LIRI-JP9123533380123533380single base substitutionGAintron_variant
LIRI-JP9123535046123535046single base substitutionTCdownstream_gene_variant
LIRI-JP9123535046123535046single base substitutionTCexon_variant
LIRI-JP9123535046123535046single base substitutionTCmissense_variantK169E505A>G
LIRI-JP9123535046123535046single base substitutionTCmissense_variantK233E697A>G
LIRI-JP9123535046123535046single base substitutionTCmissense_variantK298E892A>G
LIRI-JP9123535904123535904single base substitutionCAdownstream_gene_variant
LIRI-JP9123535904123535904single base substitutionCAintron_variant
LIRI-JP9123541504123541504single base substitutionTAintron_variant
LIRI-JP9123541504123541504single base substitutionTAupstream_gene_variant
LIRI-JP9123545933123545933single base substitutionCAdownstream_gene_variant
LIRI-JP9123545933123545933single base substitutionCAintron_variant
LIRI-JP9123547478123547478single base substitutionGAdownstream_gene_variant
LIRI-JP9123547478123547478single base substitutionGAintron_variant
LIRI-JP9123548104123548104single base substitutionCAdownstream_gene_variant
LIRI-JP9123548104123548104single base substitutionCAintron_variant
LIRI-JP9123551197123551197single base substitutionTCintron_variant
LIRI-JP9123552142123552142single base substitutionATintron_variant
LIRI-JP9123552548123552548single base substitutionGAintron_variant
LUSC-KR9123512549123512549single base substitutionGTdownstream_gene_variant
LUSC-KR9123516437123516437single base substitutionCTdownstream_gene_variant
LUSC-KR9123516437123516437single base substitutionCTintron_variant
LUSC-KR9123518367123518367single base substitutionCTdownstream_gene_variant
LUSC-KR9123518367123518367single base substitutionCTintron_variant
LUSC-KR9123521591123521591single base substitutionTC3_prime_UTR_variant
LUSC-KR9123521591123521591single base substitutionTCdownstream_gene_variant
LUSC-KR9123521591123521591single base substitutionTCintron_variant
LUSC-KR9123523655123523655single base substitutionGC3_prime_UTR_variant
LUSC-KR9123523655123523655single base substitutionGCdownstream_gene_variant
LUSC-KR9123523655123523655single base substitutionGCintron_variant
LUSC-KR9123526730123526730single base substitutionTC3_prime_UTR_variant
LUSC-KR9123526730123526730single base substitutionTCintron_variant
LUSC-KR9123532832123532832single base substitutionCGdownstream_gene_variant
LUSC-KR9123532832123532832single base substitutionCGintron_variant
LUSC-KR9123534744123534744single base substitutionCGdownstream_gene_variant
LUSC-KR9123534744123534744single base substitutionCGintron_variant
LUSC-KR9123538434123538434single base substitutionTAexon_variant
LUSC-KR9123538434123538434single base substitutionTAsynonymous_variantV123V369A>T
LUSC-KR9123538434123538434single base substitutionTAsynonymous_variantV187V561A>T
LUSC-KR9123538434123538434single base substitutionTAsynonymous_variantV252V756A>T
LUSC-KR9123538791123538791single base substitutionGAexon_variant
LUSC-KR9123538791123538791single base substitutionGAintron_variant
LUSC-KR9123538904123538904single base substitutionGTexon_variant
LUSC-KR9123538904123538904single base substitutionGTintron_variant
LUSC-KR9123545025123545025single base substitutionTAintron_variant
LUSC-KR9123555837123555837single base substitutionGTupstream_gene_variant
LUSC-KR9123558459123558459single base substitutionGCupstream_gene_variant
MALY-DE9123516696123516696single base substitutionTAdownstream_gene_variant
MALY-DE9123516696123516696single base substitutionTAintron_variant
MALY-DE9123517576123517576single base substitutionTAdownstream_gene_variant
MALY-DE9123517576123517576single base substitutionTAintron_variant
MALY-DE9123542644123542644single base substitutionAGintron_variant
MALY-DE9123542644123542644single base substitutionAGupstream_gene_variant
MALY-DE9123545274123545274single base substitutionTCintron_variant
MALY-DE9123554393123554393single base substitutionGAintron_variant
MALY-DE9123556486123556486single base substitutionTGupstream_gene_variant
MELA-AU9123509498123509498single base substitutionCTdownstream_gene_variant
MELA-AU9123509664123509664single base substitutionGAdownstream_gene_variant
MELA-AU9123509673123509673single base substitutionCTdownstream_gene_variant
MELA-AU9123509757123509757single base substitutionGAdownstream_gene_variant
MELA-AU9123509807123509807single base substitutionGAdownstream_gene_variant
MELA-AU9123510190123510190single base substitutionGAdownstream_gene_variant
MELA-AU9123510359123510359single base substitutionGAdownstream_gene_variant
MELA-AU9123510537123510537single base substitutionGAdownstream_gene_variant
MELA-AU9123510643123510643single base substitutionCTdownstream_gene_variant
MELA-AU9123510740123510740single base substitutionGAdownstream_gene_variant
MELA-AU9123510818123510818single base substitutionGAdownstream_gene_variant
MELA-AU9123511572123511572single base substitutionGAdownstream_gene_variant
MELA-AU9123511679123511679single base substitutionCTdownstream_gene_variant
MELA-AU9123511894123511894single base substitutionAGdownstream_gene_variant
MELA-AU9123512054123512054single base substitutionCTdownstream_gene_variant
MELA-AU9123512146123512146single base substitutionGAdownstream_gene_variant
MELA-AU9123513226123513226single base substitutionCTdownstream_gene_variant
MELA-AU9123513948123513948single base substitutionCTdownstream_gene_variant
MELA-AU9123514183123514183single base substitutionGAdownstream_gene_variant
MELA-AU9123514921123514921single base substitutionGAdownstream_gene_variant
MELA-AU9123514921123514921single base substitutionGAexon_variant
MELA-AU9123515582123515582single base substitutionCTdownstream_gene_variant
MELA-AU9123515582123515582single base substitutionCTexon_variant
MELA-AU9123516072123516072single base substitutionGTdownstream_gene_variant
MELA-AU9123516072123516072single base substitutionGTintron_variant
MELA-AU9123516308123516308single base substitutionCTdownstream_gene_variant
MELA-AU9123516308123516308single base substitutionCTintron_variant
MELA-AU9123516310123516310single base substitutionCAdownstream_gene_variant
MELA-AU9123516310123516310single base substitutionCAintron_variant
MELA-AU9123516759123516759single base substitutionCTdownstream_gene_variant
MELA-AU9123516759123516759single base substitutionCTintron_variant
MELA-AU9123517041123517041single base substitutionGAdownstream_gene_variant
MELA-AU9123517041123517041single base substitutionGAintron_variant
MELA-AU9123517494123517494single base substitutionCTdownstream_gene_variant
MELA-AU9123517494123517494single base substitutionCTintron_variant
MELA-AU9123517787123517787single base substitutionTGdownstream_gene_variant
MELA-AU9123517787123517787single base substitutionTGintron_variant
MELA-AU9123518294123518294single base substitutionGAdownstream_gene_variant
MELA-AU9123518294123518294single base substitutionGAintron_variant
MELA-AU9123518645123518645single base substitutionGAdownstream_gene_variant
MELA-AU9123518645123518645single base substitutionGAintron_variant
MELA-AU9123518771123518771single base substitutionCTdownstream_gene_variant
MELA-AU9123518771123518771single base substitutionCTintron_variant
MELA-AU9123519045123519045insertion of <=200bp-Adownstream_gene_variant
MELA-AU9123519045123519045insertion of <=200bp-Aintron_variant
MELA-AU9123519296123519296single base substitutionGA3_prime_UTR_variant
MELA-AU9123519296123519296single base substitutionGAintron_variant
MELA-AU9123519406123519406single base substitutionTC3_prime_UTR_variant
MELA-AU9123519406123519406single base substitutionTCintron_variant
MELA-AU9123520056123520056single base substitutionGA3_prime_UTR_variant
MELA-AU9123520056123520056single base substitutionGAintron_variant
MELA-AU9123520478123520478single base substitutionGA3_prime_UTR_variant
MELA-AU9123520478123520478single base substitutionGAintron_variant
MELA-AU9123520704123520704single base substitutionGA3_prime_UTR_variant
MELA-AU9123520704123520704single base substitutionGAintron_variant
MELA-AU9123521178123521178single base substitutionGA3_prime_UTR_variant
MELA-AU9123521178123521178single base substitutionGAintron_variant
MELA-AU9123521179123521179single base substitutionGA3_prime_UTR_variant
MELA-AU9123521179123521179single base substitutionGAintron_variant
MELA-AU9123521440123521440single base substitutionGA3_prime_UTR_variant
MELA-AU9123521440123521440single base substitutionGAintron_variant
MELA-AU9123521441123521441single base substitutionGA3_prime_UTR_variant
MELA-AU9123521441123521441single base substitutionGAintron_variant
MELA-AU9123522883123522884multiple base substitution (>=2bp and <=200bp)GGAA3_prime_UTR_variant
MELA-AU9123522883123522884multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU9123522883123522884multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU9123522918123522918single base substitutionAC3_prime_UTR_variant
MELA-AU9123522918123522918single base substitutionACdownstream_gene_variant
MELA-AU9123522918123522918single base substitutionACintron_variant
MELA-AU9123523233123523233single base substitutionGA3_prime_UTR_variant
MELA-AU9123523233123523233single base substitutionGAdownstream_gene_variant
MELA-AU9123523233123523233single base substitutionGAintron_variant
MELA-AU9123523655123523656multiple base substitution (>=2bp and <=200bp)GGAA3_prime_UTR_variant
MELA-AU9123523655123523656multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU9123523655123523656multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU9123525537123525537single base substitutionTA3_prime_UTR_variant
MELA-AU9123525537123525537single base substitutionTAdownstream_gene_variant
MELA-AU9123525537123525537single base substitutionTAintron_variant
MELA-AU9123526598123526598single base substitutionAC3_prime_UTR_variant
MELA-AU9123526598123526598single base substitutionACintron_variant
MELA-AU9123527093123527093single base substitutionGAintron_variant
MELA-AU9123527093123527093single base substitutionGAmissense_variantA305V914C>T
MELA-AU9123527093123527093single base substitutionGAmissense_variantA370V1109C>T
MELA-AU9123528126123528127multiple base substitution (>=2bp and <=200bp)GGCAintron_variant
MELA-AU9123528213123528213single base substitutionGAintron_variant
MELA-AU9123531121123531121single base substitutionGAdownstream_gene_variant
MELA-AU9123531121123531121single base substitutionGAintron_variant
MELA-AU9123531589123531589single base substitutionGAdownstream_gene_variant
MELA-AU9123531589123531589single base substitutionGAintron_variant
MELA-AU9123531600123531600single base substitutionGAdownstream_gene_variant
MELA-AU9123531600123531600single base substitutionGAintron_variant
MELA-AU9123531774123531774single base substitutionCTdownstream_gene_variant
MELA-AU9123531774123531774single base substitutionCTintron_variant
MELA-AU9123532036123532036single base substitutionGAdownstream_gene_variant
MELA-AU9123532036123532036single base substitutionGAintron_variant
MELA-AU9123532549123532549single base substitutionGAdownstream_gene_variant
MELA-AU9123532549123532549single base substitutionGAintron_variant
MELA-AU9123532914123532914single base substitutionGAdownstream_gene_variant
MELA-AU9123532914123532914single base substitutionGAintron_variant
MELA-AU9123533051123533051single base substitutionCTdownstream_gene_variant
MELA-AU9123533051123533051single base substitutionCTintron_variant
MELA-AU9123534056123534056single base substitutionGAdownstream_gene_variant
MELA-AU9123534056123534056single base substitutionGAintron_variant
MELA-AU9123535088123535088single base substitutionGAdownstream_gene_variant
MELA-AU9123535088123535088single base substitutionGAexon_variant
MELA-AU9123535088123535088single base substitutionGAmissense_variantL155F463C>T
MELA-AU9123535088123535088single base substitutionGAmissense_variantL219F655C>T
MELA-AU9123535088123535088single base substitutionGAmissense_variantL284F850C>T
MELA-AU9123536684123536684single base substitutionGAdownstream_gene_variant
MELA-AU9123536684123536684single base substitutionGAintron_variant
MELA-AU9123537542123537542single base substitutionGAdownstream_gene_variant
MELA-AU9123537542123537542single base substitutionGAintron_variant
MELA-AU9123537748123537748single base substitutionGAdownstream_gene_variant
MELA-AU9123537748123537748single base substitutionGAintron_variant
MELA-AU9123538854123538854single base substitutionGAexon_variant
MELA-AU9123538854123538854single base substitutionGAintron_variant
MELA-AU9123540095123540095single base substitutionAGintron_variant
MELA-AU9123540095123540095single base substitutionAGupstream_gene_variant
MELA-AU9123540346123540346single base substitutionGAintron_variant
MELA-AU9123540346123540346single base substitutionGAupstream_gene_variant
MELA-AU9123540815123540815single base substitutionCTexon_variant
MELA-AU9123540815123540815single base substitutionCTintron_variant
MELA-AU9123540815123540815single base substitutionCTmissense_variantD167N499G>A
MELA-AU9123540815123540815single base substitutionCTmissense_variantD38N112G>A
MELA-AU9123540815123540815single base substitutionCTupstream_gene_variant
MELA-AU9123540841123540841single base substitutionGAintron_variant
MELA-AU9123540841123540841single base substitutionGAupstream_gene_variant
MELA-AU9123541388123541388single base substitutionGAintron_variant
MELA-AU9123541388123541388single base substitutionGAupstream_gene_variant
MELA-AU9123541646123541646single base substitutionGAintron_variant
MELA-AU9123541646123541646single base substitutionGAupstream_gene_variant
MELA-AU9123541661123541661single base substitutionGAintron_variant
MELA-AU9123541661123541661single base substitutionGAupstream_gene_variant
MELA-AU9123541883123541883single base substitutionGAintron_variant
MELA-AU9123541883123541883single base substitutionGAupstream_gene_variant
MELA-AU9123541886123541886single base substitutionGAintron_variant
MELA-AU9123541886123541886single base substitutionGAupstream_gene_variant
MELA-AU9123542148123542148single base substitutionGAintron_variant
MELA-AU9123542148123542148single base substitutionGAupstream_gene_variant
MELA-AU9123542490123542490single base substitutionGCintron_variant
MELA-AU9123542490123542490single base substitutionGCupstream_gene_variant
MELA-AU9123543068123543068single base substitutionGAintron_variant
MELA-AU9123543068123543068single base substitutionGAupstream_gene_variant
MELA-AU9123543590123543590single base substitutionGAintron_variant
MELA-AU9123543590123543590single base substitutionGAupstream_gene_variant
MELA-AU9123543987123543987single base substitutionGAintron_variant
MELA-AU9123544337123544337single base substitutionTCintron_variant
MELA-AU9123544661123544661single base substitutionTAintron_variant
MELA-AU9123546589123546589single base substitutionATdownstream_gene_variant
MELA-AU9123546589123546589single base substitutionATintron_variant
MELA-AU9123547860123547860single base substitutionGAdownstream_gene_variant
MELA-AU9123547860123547860single base substitutionGAintron_variant
MELA-AU9123548089123548089single base substitutionGAdownstream_gene_variant
MELA-AU9123548089123548089single base substitutionGAintron_variant
MELA-AU9123548395123548395single base substitutionGAdownstream_gene_variant
MELA-AU9123548395123548395single base substitutionGAintron_variant
MELA-AU9123548940123548940single base substitutionGAdownstream_gene_variant
MELA-AU9123548940123548940single base substitutionGAintron_variant
MELA-AU9123549043123549043single base substitutionGAdownstream_gene_variant
MELA-AU9123549043123549043single base substitutionGAintron_variant
MELA-AU9123549132123549132single base substitutionGAdownstream_gene_variant
MELA-AU9123549132123549132single base substitutionGAintron_variant
MELA-AU9123549489123549489single base substitutionTGdownstream_gene_variant
MELA-AU9123549489123549489single base substitutionTGintron_variant
MELA-AU9123549496123549496single base substitutionGAdownstream_gene_variant
MELA-AU9123549496123549496single base substitutionGAintron_variant
MELA-AU9123549551123549551single base substitutionCGdownstream_gene_variant
MELA-AU9123549551123549551single base substitutionCGintron_variant
MELA-AU9123549902123549902single base substitutionGAdownstream_gene_variant
MELA-AU9123549902123549902single base substitutionGAintron_variant
MELA-AU9123550874123550874single base substitutionAGintron_variant
MELA-AU9123552615123552616multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU9123552655123552655single base substitutionGAintron_variant
MELA-AU9123554578123554578single base substitutionAGintron_variant
MELA-AU9123555736123555736single base substitutionGAupstream_gene_variant
MELA-AU9123555839123555839single base substitutionCTupstream_gene_variant
MELA-AU9123555848123555848single base substitutionCTupstream_gene_variant
MELA-AU9123556088123556088single base substitutionATupstream_gene_variant
MELA-AU9123556971123556971single base substitutionCTupstream_gene_variant
MELA-AU9123558174123558174single base substitutionCTupstream_gene_variant
MELA-AU9123559666123559666single base substitutionCTupstream_gene_variant
MELA-AU9123560069123560069single base substitutionAGupstream_gene_variant
MELA-AU9123560461123560461single base substitutionCTupstream_gene_variant
ORCA-IN9123513277123513277single base substitutionGAdownstream_gene_variant
ORCA-IN9123517908123517908single base substitutionGCdownstream_gene_variant
ORCA-IN9123517908123517908single base substitutionGCintron_variant
ORCA-IN9123529082123529082single base substitutionCAdownstream_gene_variant
ORCA-IN9123529082123529082single base substitutionCAintron_variant
ORCA-IN9123544297123544297single base substitutionGCintron_variant
OV-AU9123518028123518028single base substitutionCGdownstream_gene_variant
OV-AU9123518028123518028single base substitutionCGintron_variant
OV-AU9123534174123534174single base substitutionTCdownstream_gene_variant
OV-AU9123534174123534174single base substitutionTCintron_variant
OV-AU9123534229123534229single base substitutionTAdownstream_gene_variant
OV-AU9123534229123534229single base substitutionTAintron_variant
OV-AU9123534482123534482single base substitutionTAdownstream_gene_variant
OV-AU9123534482123534482single base substitutionTAintron_variant
OV-AU9123539038123539038single base substitutionCTintron_variant
OV-AU9123539038123539038single base substitutionCTupstream_gene_variant
OV-AU9123543426123543426single base substitutionGTintron_variant
OV-AU9123543426123543426single base substitutionGTupstream_gene_variant
OV-AU9123544778123544778single base substitutionGTintron_variant
OV-AU9123546923123546923single base substitutionTGdownstream_gene_variant
OV-AU9123546923123546923single base substitutionTGintron_variant
OV-AU9123548045123548045single base substitutionCTdownstream_gene_variant
OV-AU9123548045123548045single base substitutionCTintron_variant
OV-AU9123553081123553081single base substitutionGTintron_variant
PACA-AU9123516710123516710single base substitutionGAdownstream_gene_variant
PACA-AU9123516710123516710single base substitutionGAintron_variant
PACA-AU9123517221123517221single base substitutionTAdownstream_gene_variant
PACA-AU9123517221123517221single base substitutionTAintron_variant
PACA-AU9123532017123532017single base substitutionATdownstream_gene_variant
PACA-AU9123532017123532017single base substitutionATintron_variant
PACA-AU9123542289123542289single base substitutionGAintron_variant
PACA-AU9123542289123542289single base substitutionGAupstream_gene_variant
PACA-AU9123543911123543911single base substitutionCTintron_variant
PACA-AU9123543911123543911single base substitutionCTupstream_gene_variant
PACA-AU9123543917123543917single base substitutionCTintron_variant
PACA-AU9123543917123543917single base substitutionCTupstream_gene_variant
PACA-AU9123550733123550733single base substitutionCAintron_variant
PACA-AU9123550734123550734single base substitutionAGintron_variant
PACA-AU9123556764123556764single base substitutionGAupstream_gene_variant
PACA-AU9123557436123557436single base substitutionTAupstream_gene_variant
PACA-AU9123557731123557731single base substitutionTAupstream_gene_variant
PACA-AU9123559035123559035single base substitutionCTupstream_gene_variant
PACA-CA9123511707123511707single base substitutionCTdownstream_gene_variant
PACA-CA9123516130123516130single base substitutionTCdownstream_gene_variant
PACA-CA9123516130123516130single base substitutionTCintron_variant
PACA-CA9123516910123516910deletion of <=200bpT-downstream_gene_variant
PACA-CA9123516910123516910deletion of <=200bpT-intron_variant
PACA-CA9123522044123522044deletion of <=200bpT-3_prime_UTR_variant
PACA-CA9123522044123522044deletion of <=200bpT-downstream_gene_variant
PACA-CA9123522044123522044deletion of <=200bpT-intron_variant
PACA-CA9123522046123522047deletion of <=200bpAT-3_prime_UTR_variant
PACA-CA9123522046123522047deletion of <=200bpAT-downstream_gene_variant
PACA-CA9123522046123522047deletion of <=200bpAT-intron_variant
PACA-CA9123522511123522511single base substitutionGA3_prime_UTR_variant
PACA-CA9123522511123522511single base substitutionGAdownstream_gene_variant
PACA-CA9123522511123522511single base substitutionGAintron_variant
PACA-CA9123527479123527479single base substitutionTAintron_variant
PACA-CA9123528513123528513single base substitutionGAintron_variant
PACA-CA9123528743123528743single base substitutionTAdownstream_gene_variant
PACA-CA9123528743123528743single base substitutionTAintron_variant
PACA-CA9123530180123530180single base substitutionGTdownstream_gene_variant
PACA-CA9123530180123530180single base substitutionGTintron_variant
PACA-CA9123537448123537448single base substitutionCAdownstream_gene_variant
PACA-CA9123537448123537448single base substitutionCAintron_variant
PACA-CA9123541095123541095single base substitutionATintron_variant
PACA-CA9123541095123541095single base substitutionATupstream_gene_variant
PACA-CA9123547015123547015single base substitutionTCdownstream_gene_variant
PACA-CA9123547015123547015single base substitutionTCintron_variant
PACA-CA9123549554123549554single base substitutionGAdownstream_gene_variant
PACA-CA9123549554123549554single base substitutionGAintron_variant
PACA-CA9123551000123551000single base substitutionCTintron_variant
PACA-CA9123554831123554831deletion of <=200bpA-intron_variant
PACA-CA9123557492123557492single base substitutionTCupstream_gene_variant
PACA-CA9123558471123558471deletion of <=200bpA-upstream_gene_variant
PACA-CA9123559036123559036single base substitutionTGupstream_gene_variant
PAEN-AU9123535132123535132single base substitutionCAdownstream_gene_variant
PAEN-AU9123535132123535132single base substitutionCAintron_variant
PAEN-AU9123551430123551430single base substitutionGTintron_variant
PAEN-IT9123515401123515401single base substitutionCAdownstream_gene_variant
PAEN-IT9123515401123515401single base substitutionCAexon_variant
PBCA-DE9123510314123510314single base substitutionGAdownstream_gene_variant
PBCA-DE9123516976123516976single base substitutionGAdownstream_gene_variant
PBCA-DE9123516976123516976single base substitutionGAintron_variant
PBCA-DE9123533777123533777single base substitutionCAdownstream_gene_variant
PBCA-DE9123533777123533777single base substitutionCAexon_variant
PBCA-DE9123533777123533777single base substitutionCAstop_gainedE180*538G>T
PBCA-DE9123533777123533777single base substitutionCAstop_gainedE244*730G>T
PBCA-DE9123533777123533777single base substitutionCAstop_gainedE309*925G>T
PBCA-DE9123535786123535786insertion of <=200bp-Gdownstream_gene_variant
PBCA-DE9123535786123535786insertion of <=200bp-Gintron_variant
PBCA-DE9123540600123540600single base substitutionGTintron_variant
PBCA-DE9123540600123540600single base substitutionGTupstream_gene_variant
PBCA-DE9123555602123555602single base substitutionTCexon_variant
PBCA-DE9123555602123555602single base substitutionTCintron_variant
PRAD-CA9123532637123532637single base substitutionGAdownstream_gene_variant
PRAD-CA9123532637123532637single base substitutionGAintron_variant
PRAD-UK9123518901123518901single base substitutionTCdownstream_gene_variant
PRAD-UK9123518901123518901single base substitutionTCintron_variant
PRAD-UK9123529155123529155single base substitutionTAdownstream_gene_variant
PRAD-UK9123529155123529155single base substitutionTAintron_variant
PRAD-UK9123538800123538800single base substitutionGAexon_variant
PRAD-UK9123538800123538800single base substitutionGAintron_variant
PRAD-UK9123548143123548143single base substitutionCAdownstream_gene_variant
PRAD-UK9123548143123548143single base substitutionCAintron_variant
PRAD-UK9123548669123548669single base substitutionGAdownstream_gene_variant
PRAD-UK9123548669123548669single base substitutionGAintron_variant
RECA-EU9123523985123523985single base substitutionCA3_prime_UTR_variant
RECA-EU9123523985123523985single base substitutionCAdownstream_gene_variant
RECA-EU9123523985123523985single base substitutionCAintron_variant
RECA-EU9123536278123536278single base substitutionGTdownstream_gene_variant
RECA-EU9123536278123536278single base substitutionGTintron_variant
RECA-EU9123540678123540678single base substitutionTCexon_variant
RECA-EU9123540678123540678single base substitutionTCintron_variant
RECA-EU9123540678123540678single base substitutionTCsynonymous_variantE212E636A>G
RECA-EU9123540678123540678single base substitutionTCsynonymous_variantE83E249A>G
RECA-EU9123540678123540678single base substitutionTCupstream_gene_variant
RECA-EU9123540687123540687single base substitutionAGexon_variant
RECA-EU9123540687123540687single base substitutionAGintron_variant
RECA-EU9123540687123540687single base substitutionAGsynonymous_variantA209A627T>C
RECA-EU9123540687123540687single base substitutionAGsynonymous_variantA80A240T>C
RECA-EU9123540687123540687single base substitutionAGupstream_gene_variant
RECA-EU9123540732123540732single base substitutionAGexon_variant
RECA-EU9123540732123540732single base substitutionAGintron_variant
RECA-EU9123540732123540732single base substitutionAGsynonymous_variantF194F582T>C
RECA-EU9123540732123540732single base substitutionAGsynonymous_variantF65F195T>C
RECA-EU9123540732123540732single base substitutionAGupstream_gene_variant
RECA-EU9123540741123540741single base substitutionCAexon_variant
RECA-EU9123540741123540741single base substitutionCAintron_variant
RECA-EU9123540741123540741single base substitutionCAsynonymous_variantA191A573G>T
RECA-EU9123540741123540741single base substitutionCAsynonymous_variantA62A186G>T
RECA-EU9123540741123540741single base substitutionCAupstream_gene_variant
SKCA-BR9123509481123509481single base substitutionGAdownstream_gene_variant
SKCA-BR9123511105123511105single base substitutionGAdownstream_gene_variant
SKCA-BR9123512452123512452single base substitutionGAdownstream_gene_variant
SKCA-BR9123514272123514272single base substitutionGTdownstream_gene_variant
SKCA-BR9123514272123514272single base substitutionGTexon_variant
SKCA-BR9123515077123515077single base substitutionGTdownstream_gene_variant
SKCA-BR9123515077123515077single base substitutionGTexon_variant
SKCA-BR9123516414123516414insertion of <=200bp-CTdownstream_gene_variant
SKCA-BR9123516414123516414insertion of <=200bp-CTintron_variant
SKCA-BR9123517203123517203single base substitutionGAdownstream_gene_variant
SKCA-BR9123517203123517203single base substitutionGAintron_variant
SKCA-BR9123517209123517209single base substitutionGAdownstream_gene_variant
SKCA-BR9123517209123517209single base substitutionGAintron_variant
SKCA-BR9123519836123519836single base substitutionCT3_prime_UTR_variant
SKCA-BR9123519836123519836single base substitutionCTintron_variant
SKCA-BR9123526380123526380single base substitutionAG3_prime_UTR_variant
SKCA-BR9123526380123526380single base substitutionAGdownstream_gene_variant
SKCA-BR9123526380123526380single base substitutionAGintron_variant
SKCA-BR9123527252123527252single base substitutionGAintron_variant
SKCA-BR9123537165123537165single base substitutionCAdownstream_gene_variant
SKCA-BR9123537165123537165single base substitutionCAintron_variant
SKCA-BR9123539597123539597single base substitutionGAintron_variant
SKCA-BR9123539597123539597single base substitutionGAupstream_gene_variant
SKCA-BR9123539981123539981single base substitutionTCintron_variant
SKCA-BR9123539981123539981single base substitutionTCupstream_gene_variant
SKCA-BR9123540000123540000insertion of <=200bp-CCAAintron_variant
SKCA-BR9123540000123540000insertion of <=200bp-CCAAupstream_gene_variant
SKCA-BR9123540310123540310single base substitutionGAintron_variant
SKCA-BR9123540310123540310single base substitutionGAupstream_gene_variant
SKCA-BR9123542859123542859single base substitutionCTintron_variant
SKCA-BR9123542859123542859single base substitutionCTupstream_gene_variant
SKCA-BR9123543911123543911insertion of <=200bp-CATintron_variant
SKCA-BR9123543911123543911insertion of <=200bp-CATupstream_gene_variant
SKCA-BR9123543913123543913insertion of <=200bp-TATACACintron_variant
SKCA-BR9123543913123543913insertion of <=200bp-TATACACupstream_gene_variant
SKCA-BR9123543915123543915single base substitutionCTintron_variant
SKCA-BR9123543915123543915single base substitutionCTupstream_gene_variant
SKCA-BR9123546682123546682single base substitutionGAdownstream_gene_variant
SKCA-BR9123546682123546682single base substitutionGAintron_variant
SKCA-BR9123555597123555597single base substitutionTCexon_variant
SKCA-BR9123555597123555597single base substitutionTCintron_variant
SKCA-BR9123555810123555810single base substitutionAGupstream_gene_variant
SKCA-BR9123558273123558273single base substitutionTGupstream_gene_variant
SKCM-US9123527023123527023single base substitutionCTintron_variant
SKCM-US9123527023123527023single base substitutionCTsynonymous_variantR328R984G>A
SKCM-US9123527023123527023single base substitutionCTsynonymous_variantR393R1179G>A
SKCM-US9123535038123535038single base substitutionCGdownstream_gene_variant
SKCM-US9123535038123535038single base substitutionCGexon_variant
SKCM-US9123535038123535038single base substitutionCGmissense_variantE171D513G>C
SKCM-US9123535038123535038single base substitutionCGmissense_variantE235D705G>C
SKCM-US9123535038123535038single base substitutionCGmissense_variantE300D900G>C
SKCM-US9123550268123550268single base substitutionAC5_prime_UTR_variant
SKCM-US9123550268123550268single base substitutionACdownstream_gene_variant
SKCM-US9123550268123550268single base substitutionACexon_variant
SKCM-US9123550268123550268single base substitutionACmissense_variantV90G269T>G
STAD-US9123526872123526872single base substitutionTCintron_variant
STAD-US9123526872123526872single base substitutionTCmissense_variantS379G1135A>G
STAD-US9123526872123526872single base substitutionTCmissense_variantS444G1330A>G
STAD-US9123527025123527025single base substitutionGAintron_variant
STAD-US9123527025123527025single base substitutionGAmissense_variantR328W982C>T
STAD-US9123527025123527025single base substitutionGAmissense_variantR393W1177C>T
STAD-US9123527050123527050single base substitutionGAintron_variant
STAD-US9123527050123527050single base substitutionGAsynonymous_variantN319N957C>T
STAD-US9123527050123527050single base substitutionGAsynonymous_variantN384N1152C>T
STAD-US9123550083123550083single base substitutionAGdownstream_gene_variant
STAD-US9123550083123550083single base substitutionAGexon_variant
STAD-US9123550083123550083single base substitutionAGmissense_variantY152H454T>C
STAD-US9123550083123550083single base substitutionAGmissense_variantY23H67T>C
THCA-SA9123524801123524801single base substitutionAC3_prime_UTR_variant
THCA-SA9123524801123524801single base substitutionACdownstream_gene_variant
THCA-SA9123524801123524801single base substitutionACintron_variant
UCEC-US9123526843123526843single base substitutionGAintron_variant
UCEC-US9123526843123526843single base substitutionGAsynonymous_variantH388H1164C>T
UCEC-US9123526843123526843single base substitutionGAsynonymous_variantH453H1359C>T
UCEC-US9123526948123526948single base substitutionGAintron_variant
UCEC-US9123526948123526948single base substitutionGAsynonymous_variantG353G1059C>T
UCEC-US9123526948123526948single base substitutionGAsynonymous_variantG418G1254C>T
UCEC-US9123526990123526990single base substitutionTCintron_variant
UCEC-US9123526990123526990single base substitutionTCsynonymous_variantP339P1017A>G
UCEC-US9123526990123526990single base substitutionTCsynonymous_variantP404P1212A>G
UCEC-US9123535119123535119single base substitutionCAdownstream_gene_variant
UCEC-US9123535119123535119single base substitutionCAsplice_acceptor_variant
UCEC-US9123540779123540779single base substitutionGAexon_variant
UCEC-US9123540779123540779single base substitutionGAintron_variant
UCEC-US9123540779123540779single base substitutionGAstop_gainedQ179*535C>T
UCEC-US9123540779123540779single base substitutionGAstop_gainedQ50*148C>T
UCEC-US9123540779123540779single base substitutionGAupstream_gene_variant
UCEC-US9123550229123550229single base substitutionTG5_prime_UTR_variant
UCEC-US9123550229123550229single base substitutionTGdownstream_gene_variant
UCEC-US9123550229123550229single base substitutionTGexon_variant
UCEC-US9123550229123550229single base substitutionTGmissense_variantK103T308A>C
UCEC-US9123550474123550474single base substitutionCTexon_variant
UCEC-US9123550474123550474single base substitutionCTintron_variant
UCEC-US9123550474123550474single base substitutionCTsynonymous_variantT21T63G>A
UCEC-US9123550514123550514single base substitutionGAexon_variant
UCEC-US9123550514123550514single base substitutionGAintron_variant
UCEC-US9123550514123550514single base substitutionGAmissense_variantT8I23C>T
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.4949859q346090712449346|CGAP|BC018738|A/G|non-coding||102|Candidate;
2449346|CGAP|BC110334|A/G|non-coding||86|Candidate
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGMissensep.Y152Hc.454T>C9123550083STAD
CAMissensep.G307Wc.919G>T9123533783CLL
CASpliceAcceptorSNV.c.820-1G>T9123535119LUAD
CASpliceAcceptorSNV.c.820-1G>T9123535119UCEC
CCTTMissensep.D115Nc.342_343delinsAA9123550194CM
CGMissensep.K198Nc.594G>C9123540720ESCA
CTMissensep.G375Ec.1124G>A9123527078CM
CTMissensep.G454Sc.1360G>A9123526842BRCA
CTSynonymousp.K120Kc.360G>A9123550177HNSC
GA5-UTRSNV.c.1-10C>T9123550546CM
GAMissensep.S343Lc.1028C>T9123533674BRCA
GANonsensep.Q179*c.535C>T9123540779UCEC
GCMissensep.L261Vc.781C>G9123538409OV
GCMissensep.S84Cc.251C>G9123550286BRCA
GCSynonymousp.L57Lc.171C>G9123550366BLCA
GT3-UTRSNV.c.1362+65C>A9123526775CM
TCMissensep.S444Gc.1330A>G9123526872STAD
TGMissensep.K273Qc.817A>C9123538373ESCA