FBXO32
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA8124516888124516888+Missense_MutationSNPCCGTCGA-DK-A3X1-01A-12D-A22Z-08TCGA-DK-A3X1-10A-01D-A22Z-08g.chr8:124516888C>Gc.934G>Cc.(934-936)Gat>Catp.D312H
BLCA8124525536124525536+Missense_MutationSNPCCTTCGA-UY-A9PD-01A-11D-A38G-08TCGA-UY-A9PD-10A-01D-A38J-08g.chr8:124525536C>Tc.553G>Ac.(553-555)Ggc>Agcp.G185S
BLCA8124525576124525576+SilentSNPCCTTCGA-ZF-A9RC-01A-11D-A38G-08TCGA-ZF-A9RC-10A-01D-A38J-08g.chr8:124525576C>Tc.513G>Ac.(511-513)caG>caAp.Q171Q
BLCA8124553195124553195+SilentSNPGGATCGA-KQ-A41R-01A-21D-A34U-08TCGA-KQ-A41R-10G-01D-A34X-08g.chr8:124553195G>Ac.60C>Tc.(58-60)gaC>gaTp.D20D
BRCA8124518725124518725+SilentSNPGGTTCGA-B6-A0I1-01A-11D-A21Q-09TCGA-B6-A0I1-10A-01D-A21Q-09g.chr8:124518725G>Tc.741C>Ac.(739-741)gtC>gtAp.V247V
BRCA8124526556124526556+SilentSNPTTCTCGA-D8-A1JC-01A-11D-A13L-09TCGA-D8-A1JC-10A-01D-A13O-09g.chr8:124526556T>Cc.390A>Gc.(388-390)gcA>gcGp.A130A
BRCA8124544170124544170+Missense_MutationSNPGGCTCGA-EW-A1J5-01A-11D-A13L-09TCGA-EW-A1J5-10A-01D-A13O-09g.chr8:124544170G>Cc.340C>Gc.(340-342)Ctg>Gtgp.L114V
CESC8124516928124516928+Missense_MutationSNPGGCTCGA-WL-A834-01A-11D-A351-09TCGA-WL-A834-10A-01D-A351-09g.chr8:124516928G>Cc.894C>Gc.(892-894)ttC>ttGp.F298L
COAD8124515668124515668+Missense_MutationSNPTTCTCGA-D5-6898-01A-11D-1924-10TCGA-D5-6898-10A-01D-1924-10g.chr8:124515668T>Cc.1013A>Gc.(1012-1014)gAg>gGgp.E338G
COAD8124518759124518759+Missense_MutationSNPAAGTCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr8:124518759A>Gc.707T>Cc.(706-708)aTc>aCcp.I236T
COAD8124525479124525479+Missense_MutationSNPGGTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr8:124525479G>Tc.610C>Ac.(610-612)Ctc>Atcp.L204I
COAD8124525494124525494+Missense_MutationSNPGGATCGA-AA-3984-01A-02W-0995-10TCGA-AA-3984-10A-01W-0999-10g.chr8:124525494G>Ac.595C>Tc.(595-597)Cgg>Tggp.R199W
COAD8124525568124525568+Missense_MutationSNPTTCTCGA-AA-A00E-01A-01W-A005-10TCGA-AA-A00E-10A-01W-A005-10g.chr8:124525568T>Cc.521A>Gc.(520-522)tAc>tGcp.Y174C
COAD8124544146124544146+Missense_MutationSNPCCTTCGA-AA-3966-01A-01W-1073-09TCGA-AA-3966-10A-01W-1073-09g.chr8:124544146C>Tc.364G>Ac.(364-366)Gtg>Atgp.V122M
COAD8124545463124545464+Frame_Shift_InsINS--TTCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr8:124545463_124545464insTc.246_247insAc.(244-249)aaatggfsp.W83fs
COADREAD8124515668124515668+Missense_MutationSNPTTCTCGA-D5-6898-01A-11D-1924-10TCGA-D5-6898-10A-01D-1924-10g.chr8:124515668T>Cc.1013A>Gc.(1012-1014)gAg>gGgp.E338G
COADREAD8124516969124516969+Missense_MutationSNPGGTTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:124516969G>Tc.853C>Ac.(853-855)Ctg>Atgp.L285M
COADREAD8124518759124518759+Missense_MutationSNPAAGTCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr8:124518759A>Gc.707T>Cc.(706-708)aTc>aCcp.I236T
COADREAD8124525479124525479+Missense_MutationSNPGGTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr8:124525479G>Tc.610C>Ac.(610-612)Ctc>Atcp.L204I
COADREAD8124525494124525494+Missense_MutationSNPGGATCGA-AA-3984-01A-02W-0995-10TCGA-AA-3984-10A-01W-0999-10g.chr8:124525494G>Ac.595C>Tc.(595-597)Cgg>Tggp.R199W
COADREAD8124525568124525568+Missense_MutationSNPTTCTCGA-AA-A00E-01A-01W-A005-10TCGA-AA-A00E-10A-01W-A005-10g.chr8:124525568T>Cc.521A>Gc.(520-522)tAc>tGcp.Y174C
COADREAD8124544146124544146+Missense_MutationSNPCCTTCGA-AA-3966-01A-01W-1073-09TCGA-AA-3966-10A-01W-1073-09g.chr8:124544146C>Tc.364G>Ac.(364-366)Gtg>Atgp.V122M
COADREAD8124545463124545464+Frame_Shift_InsINS--TTCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr8:124545463_124545464insTc.246_247insAc.(244-249)aaatggfsp.W83fs
GBM8124518764124518764+SilentSNPCCTTCGA-06-0130-01A-01D-1490-08TCGA-06-0130-10A-01D-1490-08g.chr8:124518764C>Tc.702G>Ac.(700-702)ctG>ctAp.L234L
GBMLGG8124518764124518764+SilentSNPCCTTCGA-06-0130-01A-01D-1490-08TCGA-06-0130-10A-01D-1490-08g.chr8:124518764C>Tc.702G>Ac.(700-702)ctG>ctAp.L234L
HNSC8124515703124515703+Splice_SiteSNPCCATCGA-UF-A7JV-01A-11D-A34J-08TCGA-UF-A7JV-10A-01D-A34M-08g.chr8:124515703C>Ac.e9-1
HNSC8124526525124526525+Missense_MutationSNPCCTTCGA-CX-7086-01A-11D-2078-08TCGA-CX-7086-10D-01D-2078-08g.chr8:124526525C>Tc.421G>Ac.(421-423)Gcc>Accp.A141T
LIHC8124553194124553194+Missense_MutationSNPCCTTCGA-CC-A7IJ-01A-11D-A33Q-10TCGA-CC-A7IJ-10A-01D-A33Q-10g.chr8:124553194C>Tc.61G>Ac.(61-63)Ggc>Agcp.G21S
LUAD8124546959124546959+Missense_MutationSNPCCTTCGA-44-7669-01A-21D-2063-08TCGA-44-7669-10A-01D-2063-08g.chr8:124546959C>Tc.212G>Ac.(211-213)aGc>aAcp.S71N
LUSC8124546943124546943+Splice_SiteSNPCCATCGA-85-6561-01A-11D-1817-08TCGA-85-6561-10A-01D-1817-08g.chr8:124546943C>Ac.228G>Tc.(226-228)caG>caTp.Q76H
LUSC8124547001124547001+Missense_MutationSNPTTCTCGA-22-5473-01A-01D-1632-08TCGA-22-5473-11A-11D-1632-08g.chr8:124547001T>Cc.170A>Gc.(169-171)tAt>tGtp.Y57C
LUSC8124553144124553144+SilentSNPGGATCGA-33-4583-01A-01D-1441-08TCGA-33-4583-11A-01D-1441-08g.chr8:124553144G>Ac.111C>Tc.(109-111)ctC>ctTp.L37L
LUSC8124553156124553156+SilentSNPGGATCGA-37-3783-01A-01D-1267-08TCGA-37-3783-10A-01D-1267-08g.chr8:124553156G>Ac.99C>Tc.(97-99)ttC>ttTp.F33F
PCPG8124526522124526522+Missense_MutationSNPGGCTCGA-QR-A705-01A-11D-A35D-08TCGA-QR-A705-10A-01D-A35B-08g.chr8:124526522G>Cc.424C>Gc.(424-426)Caa>Gaap.Q142E
PRAD8124547022124547022+Missense_MutationSNPTTGTCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr8:124547022T>Gc.149A>Cc.(148-150)aAt>aCtp.N50T
READ8124516969124516969+Missense_MutationSNPGGTTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:124516969G>Tc.853C>Ac.(853-855)Ctg>Atgp.L285M
SKCM8124518738124518738+Missense_MutationSNPCCTTCGA-D3-A2JL-06A-11D-A196-08TCGA-D3-A2JL-10A-01D-A198-08g.chr8:124518738C>Tc.728G>Ac.(727-729)gGg>gAgp.G243E
SKCM8124518793124518793+Missense_MutationSNPAAGTCGA-EB-A5UL-06A-11D-A30X-08TCGA-EB-A5UL-10A-01D-A30X-08g.chr8:124518793A>Gc.673T>Cc.(673-675)Ttc>Ctcp.F225L
SKCM8124518802124518802+Missense_MutationSNPCCTTCGA-ER-A19N-06A-11D-A197-08TCGA-ER-A19N-10A-01D-A199-08g.chr8:124518802C>Tc.664G>Ac.(664-666)Ggc>Agcp.G222S
SKCM8124553147124553147+SilentSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr8:124553147G>Ac.108C>Tc.(106-108)gaC>gaTp.D36D
SKCM8124553243124553243+SilentSNPGGATCGA-EE-A3JD-06A-11D-A20D-08TCGA-EE-A3JD-10A-01D-A20D-08g.chr8:124553243G>Ac.12C>Tc.(10-12)ctC>ctTp.L4L
SKCM8124553245124553245+Missense_MutationSNPGGATCGA-EE-A3JD-06A-11D-A20D-08TCGA-EE-A3JD-10A-01D-A20D-08g.chr8:124553245G>Ac.10C>Tc.(10-12)Ctc>Ttcp.L4F
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-CN8124544186124544186single base substitutionGAexon_variant
BLCA-CN8124544186124544186single base substitutionGAsynonymous_variantD108D324C>T
BLCA-CN8124553171124553171single base substitutionCGexon_variant
BLCA-CN8124553171124553171single base substitutionCGmissense_variantE28D84G>C
BLCA-US8124516888124516888single base substitutionCGexon_variant
BLCA-US8124516888124516888single base substitutionCGmissense_variantD219H655G>C
BLCA-US8124516888124516888single base substitutionCGmissense_variantD312H934G>C
BOCA-FR8124539766124539766single base substitutionGCintron_variant
BRCA-EU8124506694124506694single base substitutionTCdownstream_gene_variant
BRCA-EU8124506813124506813single base substitutionGCdownstream_gene_variant
BRCA-EU8124508979124508979single base substitutionCTdownstream_gene_variant
BRCA-EU8124509485124509485single base substitutionCTdownstream_gene_variant
BRCA-EU8124510689124510689single base substitutionGC3_prime_UTR_variant
BRCA-EU8124510689124510689single base substitutionGCdownstream_gene_variant
BRCA-EU8124513729124513729single base substitutionGT3_prime_UTR_variant
BRCA-EU8124513729124513729single base substitutionGTdownstream_gene_variant
BRCA-EU8124513742124513742single base substitutionCT3_prime_UTR_variant
BRCA-EU8124513742124513742single base substitutionCTdownstream_gene_variant
BRCA-EU8124515146124515146single base substitutionGC3_prime_UTR_variant
BRCA-EU8124515146124515146single base substitutionGCdownstream_gene_variant
BRCA-EU8124517184124517184single base substitutionCGintron_variant
BRCA-EU8124519182124519182single base substitutionCTintron_variant
BRCA-EU8124519182124519182single base substitutionCTupstream_gene_variant
BRCA-EU8124520505124520505single base substitutionCTintron_variant
BRCA-EU8124520505124520505single base substitutionCTupstream_gene_variant
BRCA-EU8124521597124521597single base substitutionCTdownstream_gene_variant
BRCA-EU8124521597124521597single base substitutionCTintron_variant
BRCA-EU8124521597124521597single base substitutionCTupstream_gene_variant
BRCA-EU8124521638124521638single base substitutionGCdownstream_gene_variant
BRCA-EU8124521638124521638single base substitutionGCintron_variant
BRCA-EU8124521638124521638single base substitutionGCupstream_gene_variant
BRCA-EU8124521706124521706single base substitutionGAdownstream_gene_variant
BRCA-EU8124521706124521706single base substitutionGAintron_variant
BRCA-EU8124521706124521706single base substitutionGAupstream_gene_variant
BRCA-EU8124522849124522849deletion of <=200bpA-downstream_gene_variant
BRCA-EU8124522849124522849deletion of <=200bpA-intron_variant
BRCA-EU8124522849124522849deletion of <=200bpA-upstream_gene_variant
BRCA-EU8124523134124523134single base substitutionGAdownstream_gene_variant
BRCA-EU8124523134124523134single base substitutionGAintron_variant
BRCA-EU8124523134124523134single base substitutionGAupstream_gene_variant
BRCA-EU8124523429124523429single base substitutionGCdownstream_gene_variant
BRCA-EU8124523429124523429single base substitutionGCintron_variant
BRCA-EU8124523429124523429single base substitutionGCupstream_gene_variant
BRCA-EU8124524605124524605single base substitutionTCdownstream_gene_variant
BRCA-EU8124524605124524605single base substitutionTCintron_variant
BRCA-EU8124526562124526562single base substitutionCTexon_variant
BRCA-EU8124526562124526562single base substitutionCTintron_variant
BRCA-EU8124526562124526562single base substitutionCTsynonymous_variantL128L384G>A
BRCA-EU8124526688124526688single base substitutionGAintron_variant
BRCA-EU8124528323124528323single base substitutionCAintron_variant
BRCA-EU8124528598124528598single base substitutionCGintron_variant
BRCA-EU8124528937124528937single base substitutionATintron_variant
BRCA-EU8124529309124529309single base substitutionCGintron_variant
BRCA-EU8124529890124529890single base substitutionGAintron_variant
BRCA-EU8124530793124530793single base substitutionAGintron_variant
BRCA-EU8124531409124531409single base substitutionATintron_variant
BRCA-EU8124532366124532366single base substitutionGCintron_variant
BRCA-EU8124533681124533681single base substitutionGAintron_variant
BRCA-EU8124533967124533968deletion of <=200bpAC-intron_variant
BRCA-EU8124534423124534423single base substitutionCAdownstream_gene_variant
BRCA-EU8124534423124534423single base substitutionCAintron_variant
BRCA-EU8124535786124535786single base substitutionCTdownstream_gene_variant
BRCA-EU8124535786124535786single base substitutionCTintron_variant
BRCA-EU8124535843124535843insertion of <=200bp-Adownstream_gene_variant
BRCA-EU8124535843124535843insertion of <=200bp-Aintron_variant
BRCA-EU8124535871124535871insertion of <=200bp-Adownstream_gene_variant
BRCA-EU8124535871124535871insertion of <=200bp-Aintron_variant
BRCA-EU8124535920124535920single base substitutionTCdownstream_gene_variant
BRCA-EU8124535920124535920single base substitutionTCintron_variant
BRCA-EU8124536166124536166single base substitutionGCdownstream_gene_variant
BRCA-EU8124536166124536166single base substitutionGCintron_variant
BRCA-EU8124538378124538378single base substitutionCTdownstream_gene_variant
BRCA-EU8124538378124538378single base substitutionCTintron_variant
BRCA-EU8124538522124538522single base substitutionGAdownstream_gene_variant
BRCA-EU8124538522124538522single base substitutionGAintron_variant
BRCA-EU8124539346124539346single base substitutionCTexon_variant
BRCA-EU8124539346124539346single base substitutionCTintron_variant
BRCA-EU8124540596124540596single base substitutionGAintron_variant
BRCA-EU8124540649124540649single base substitutionCGintron_variant
BRCA-EU8124541071124541071insertion of <=200bp-Tintron_variant
BRCA-EU8124541669124541669single base substitutionGCintron_variant
BRCA-EU8124541691124541691single base substitutionCTintron_variant
BRCA-EU8124541787124541787single base substitutionTCintron_variant
BRCA-EU8124541855124541855deletion of <=200bpC-intron_variant
BRCA-EU8124542163124542163single base substitutionGTintron_variant
BRCA-EU8124542170124542170single base substitutionGCintron_variant
BRCA-EU8124542409124542409single base substitutionCAintron_variant
BRCA-EU8124542936124542936single base substitutionCAintron_variant
BRCA-EU8124543017124543017single base substitutionGTintron_variant
BRCA-EU8124543064124543064single base substitutionGCintron_variant
BRCA-EU8124544504124544504single base substitutionTCintron_variant
BRCA-EU8124544504124544504single base substitutionTCupstream_gene_variant
BRCA-EU8124544588124544588single base substitutionTGintron_variant
BRCA-EU8124544588124544588single base substitutionTGupstream_gene_variant
BRCA-EU8124544781124544781single base substitutionGAintron_variant
BRCA-EU8124544781124544781single base substitutionGAupstream_gene_variant
BRCA-EU8124545083124545083single base substitutionCTintron_variant
BRCA-EU8124545083124545083single base substitutionCTupstream_gene_variant
BRCA-EU8124545220124545220single base substitutionCGintron_variant
BRCA-EU8124545220124545220single base substitutionCGupstream_gene_variant
BRCA-EU8124546509124546509single base substitutionTCintron_variant
BRCA-EU8124546509124546509single base substitutionTCupstream_gene_variant
BRCA-EU8124547215124547215single base substitutionCGintron_variant
BRCA-EU8124547215124547215single base substitutionCGupstream_gene_variant
BRCA-EU8124548517124548517single base substitutionTCintron_variant
BRCA-EU8124548517124548517single base substitutionTCupstream_gene_variant
BRCA-EU8124548885124548885single base substitutionGCintron_variant
BRCA-EU8124548885124548885single base substitutionGCupstream_gene_variant
BRCA-EU8124549007124549007single base substitutionGCintron_variant
BRCA-EU8124549007124549007single base substitutionGCupstream_gene_variant
BRCA-EU8124549683124549683single base substitutionGCintron_variant
BRCA-EU8124550149124550149single base substitutionAGintron_variant
BRCA-EU8124550186124550186single base substitutionGCintron_variant
BRCA-EU8124550747124550747single base substitutionAGintron_variant
BRCA-EU8124551059124551059single base substitutionGTintron_variant
BRCA-EU8124551212124551212single base substitutionGCintron_variant
BRCA-EU8124551864124551864single base substitutionGTintron_variant
BRCA-EU8124552016124552016single base substitutionGTintron_variant
BRCA-EU8124552259124552259single base substitutionGCintron_variant
BRCA-EU8124552604124552604single base substitutionTAintron_variant
BRCA-EU8124552974124552974single base substitutionGAintron_variant
BRCA-EU8124553078124553078insertion of <=200bp-Cintron_variant
BRCA-EU8124553117124553117single base substitutionACintron_variant
BRCA-EU8124553210124553210single base substitutionCAexon_variant
BRCA-EU8124553210124553210single base substitutionCAmissense_variantW15C45G>T
BRCA-EU8124553550124553550single base substitutionCAupstream_gene_variant
BRCA-EU8124553904124553904single base substitutionGTupstream_gene_variant
BRCA-EU8124554016124554016single base substitutionCAupstream_gene_variant
BRCA-EU8124557349124557349single base substitutionGAupstream_gene_variant
BRCA-EU8124558053124558053single base substitutionGCupstream_gene_variant
BRCA-FR8124521638124521638single base substitutionGCdownstream_gene_variant
BRCA-FR8124521638124521638single base substitutionGCintron_variant
BRCA-FR8124521638124521638single base substitutionGCupstream_gene_variant
BRCA-FR8124526562124526562single base substitutionCTexon_variant
BRCA-FR8124526562124526562single base substitutionCTintron_variant
BRCA-FR8124526562124526562single base substitutionCTsynonymous_variantL128L384G>A
BRCA-FR8124528323124528323single base substitutionCAintron_variant
BRCA-FR8124538378124538378single base substitutionCTdownstream_gene_variant
BRCA-FR8124538378124538378single base substitutionCTintron_variant
BRCA-FR8124541691124541691single base substitutionCTintron_variant
BRCA-FR8124542409124542409single base substitutionCAintron_variant
BRCA-FR8124547215124547215single base substitutionCGintron_variant
BRCA-FR8124547215124547215single base substitutionCGupstream_gene_variant
BRCA-FR8124554036124554036single base substitutionCGupstream_gene_variant
BRCA-US8124518725124518725single base substitutionGTexon_variant
BRCA-US8124518725124518725single base substitutionGTsynonymous_variantV154V462C>A
BRCA-US8124518725124518725single base substitutionGTsynonymous_variantV247V741C>A
BRCA-US8124526556124526556single base substitutionTCexon_variant
BRCA-US8124526556124526556single base substitutionTCintron_variant
BRCA-US8124526556124526556single base substitutionTCsynonymous_variantA130A390A>G
BRCA-US8124544170124544170single base substitutionGCexon_variant
BRCA-US8124544170124544170single base substitutionGCmissense_variantL114V340C>G
BTCA-JP8124525676124525676single base substitutionTGintron_variant
CESC-US8124516928124516928single base substitutionGCexon_variant
CESC-US8124516928124516928single base substitutionGCmissense_variantF205L615C>G
CESC-US8124516928124516928single base substitutionGCmissense_variantF298L894C>G
CLLE-ES8124516390124516390single base substitutionCTintron_variant
CLLE-ES8124530816124530816single base substitutionCTintron_variant
CLLE-ES8124534081124534081single base substitutionGAintron_variant
CLLE-ES8124547605124547605single base substitutionGAintron_variant
CLLE-ES8124547605124547605single base substitutionGAupstream_gene_variant
COAD-US8124518759124518759single base substitutionAGexon_variant
COAD-US8124518759124518759single base substitutionAGmissense_variantI143T428T>C
COAD-US8124518759124518759single base substitutionAGmissense_variantI236T707T>C
COAD-US8124525537124525537single base substitutionGAexon_variant
COAD-US8124525537124525537single base substitutionGAintron_variant
COAD-US8124525537124525537single base substitutionGAsynonymous_variantV184V552C>T
COAD-US8124545463124545463insertion of <=200bp-Texon_variant
COAD-US8124545463124545463insertion of <=200bp-Tframeshift_variantW83*?
COAD-US8124545463124545463insertion of <=200bp-Tupstream_gene_variant
COCA-CN8124505156124505156single base substitutionAGdownstream_gene_variant
COCA-CN8124510930124510930single base substitutionGA3_prime_UTR_variant
COCA-CN8124510930124510930single base substitutionGAdownstream_gene_variant
COCA-CN8124513629124513629single base substitutionCA3_prime_UTR_variant
COCA-CN8124513629124513629single base substitutionCAdownstream_gene_variant
COCA-CN8124518713124518713single base substitutionCGexon_variant
COCA-CN8124518713124518713single base substitutionCGmissense_variantQ158H474G>C
COCA-CN8124518713124518713single base substitutionCGmissense_variantQ251H753G>C
COCA-CN8124547488124547488single base substitutionGAintron_variant
COCA-CN8124547488124547488single base substitutionGAupstream_gene_variant
COCA-CN8124555319124555319single base substitutionCAupstream_gene_variant
ESAD-UK8124506128124506128single base substitutionGTdownstream_gene_variant
ESAD-UK8124506601124506601single base substitutionCTdownstream_gene_variant
ESAD-UK8124509078124509078single base substitutionCTdownstream_gene_variant
ESAD-UK8124510722124510722single base substitutionGT3_prime_UTR_variant
ESAD-UK8124510722124510722single base substitutionGTdownstream_gene_variant
ESAD-UK8124514082124514082single base substitutionAG3_prime_UTR_variant
ESAD-UK8124514082124514082single base substitutionAGdownstream_gene_variant
ESAD-UK8124515172124515172single base substitutionCG3_prime_UTR_variant
ESAD-UK8124515172124515172single base substitutionCGdownstream_gene_variant
ESAD-UK8124515658124515658single base substitutionGAexon_variant
ESAD-UK8124515658124515658single base substitutionGAsynonymous_variantS248S744C>T
ESAD-UK8124515658124515658single base substitutionGAsynonymous_variantS341S1023C>T
ESAD-UK8124515959124515959single base substitutionCTintron_variant
ESAD-UK8124517053124517053single base substitutionCTintron_variant
ESAD-UK8124517221124517221single base substitutionTCintron_variant
ESAD-UK8124517466124517466single base substitutionTGintron_variant
ESAD-UK8124519976124519976single base substitutionCAintron_variant
ESAD-UK8124519976124519976single base substitutionCAupstream_gene_variant
ESAD-UK8124520305124520305single base substitutionGAintron_variant
ESAD-UK8124520305124520305single base substitutionGAupstream_gene_variant
ESAD-UK8124520365124520387deletion of <=200bpAGGTCACAGGGGAAAAATAATAC-intron_variant
ESAD-UK8124520365124520387deletion of <=200bpAGGTCACAGGGGAAAAATAATAC-upstream_gene_variant
ESAD-UK8124525270124525270single base substitutionCGdownstream_gene_variant
ESAD-UK8124525270124525270single base substitutionCGintron_variant
ESAD-UK8124531546124531546single base substitutionCAintron_variant
ESAD-UK8124534748124534748single base substitutionCTdownstream_gene_variant
ESAD-UK8124534748124534748single base substitutionCTintron_variant
ESAD-UK8124535504124535504single base substitutionCAdownstream_gene_variant
ESAD-UK8124535504124535504single base substitutionCAintron_variant
ESAD-UK8124540996124540996single base substitutionTCintron_variant
ESAD-UK8124541563124541563single base substitutionAGintron_variant
ESAD-UK8124541724124541724single base substitutionGAintron_variant
ESAD-UK8124542805124542805single base substitutionGTintron_variant
ESAD-UK8124549347124549347single base substitutionACintron_variant
ESAD-UK8124549347124549347single base substitutionACupstream_gene_variant
ESAD-UK8124551217124551217single base substitutionCTintron_variant
ESAD-UK8124551544124551544single base substitutionATintron_variant
ESAD-UK8124552614124552614single base substitutionGCintron_variant
ESAD-UK8124553932124553932single base substitutionGCupstream_gene_variant
ESAD-UK8124555966124555966single base substitutionACupstream_gene_variant
ESAD-UK8124556374124556374single base substitutionCTupstream_gene_variant
ESAD-UK8124556705124556705single base substitutionTAupstream_gene_variant
ESAD-UK8124556979124556979single base substitutionGAupstream_gene_variant
ESAD-UK8124558345124558345deletion of <=200bpT-upstream_gene_variant
ESCA-CN8124553228124553228single base substitutionCTexon_variant
ESCA-CN8124553228124553228single base substitutionCTsynonymous_variantR9R27G>A
GACA-CN8124518736124518736single base substitutionGAexon_variant
GACA-CN8124518736124518736single base substitutionGAmissense_variantR151W451C>T
GACA-CN8124518736124518736single base substitutionGAmissense_variantR244W730C>T
GBM-US8124518764124518764single base substitutionCTexon_variant
GBM-US8124518764124518764single base substitutionCTsynonymous_variantL141L423G>A
GBM-US8124518764124518764single base substitutionCTsynonymous_variantL234L702G>A
LAML-KR8124526607124526607single base substitutionGAintron_variant
LICA-FR8124510832124510834deletion of <=200bpTAG-3_prime_UTR_variant
LICA-FR8124510832124510834deletion of <=200bpTAG-downstream_gene_variant
LICA-FR8124524848124524848single base substitutionTCdownstream_gene_variant
LICA-FR8124524848124524848single base substitutionTCintron_variant
LICA-FR8124527661124527661single base substitutionGTintron_variant
LICA-FR8124539024124539024single base substitutionACdownstream_gene_variant
LICA-FR8124539024124539024single base substitutionACintron_variant
LIHC-US8124553194124553194single base substitutionCTexon_variant
LIHC-US8124553194124553194single base substitutionCTmissense_variantG21S61G>A
LINC-JP8124509000124509000insertion of <=200bp-Tdownstream_gene_variant
LINC-JP8124514082124514082deletion of <=200bpA-3_prime_UTR_variant
LINC-JP8124514082124514082deletion of <=200bpA-downstream_gene_variant
LINC-JP8124521905124521905single base substitutionAGdownstream_gene_variant
LINC-JP8124521905124521905single base substitutionAGintron_variant
LINC-JP8124521905124521905single base substitutionAGupstream_gene_variant
LINC-JP8124529718124529718deletion of <=200bpT-intron_variant
LINC-JP8124529718124529718insertion of <=200bp-Tintron_variant
LINC-JP8124541873124541873single base substitutionTCintron_variant
LINC-JP8124543157124543157deletion of <=200bpT-intron_variant
LINC-JP8124551805124551805single base substitutionTCintron_variant
LIRI-JP8124505195124505195single base substitutionTAdownstream_gene_variant
LIRI-JP8124507313124507313single base substitutionTGdownstream_gene_variant
LIRI-JP8124509928124509928single base substitutionACdownstream_gene_variant
LIRI-JP8124511891124511891single base substitutionGT3_prime_UTR_variant
LIRI-JP8124511891124511891single base substitutionGTdownstream_gene_variant
LIRI-JP8124513958124513958single base substitutionCT3_prime_UTR_variant
LIRI-JP8124513958124513958single base substitutionCTdownstream_gene_variant
LIRI-JP8124515137124515137single base substitutionCG3_prime_UTR_variant
LIRI-JP8124515137124515137single base substitutionCGdownstream_gene_variant
LIRI-JP8124515279124515279single base substitutionAG3_prime_UTR_variant
LIRI-JP8124515279124515279single base substitutionAGdownstream_gene_variant
LIRI-JP8124516252124516252single base substitutionGCintron_variant
LIRI-JP8124518216124518216single base substitutionGAintron_variant
LIRI-JP8124518789124518789single base substitutionGTexon_variant
LIRI-JP8124518789124518789single base substitutionGTmissense_variantT133N398C>A
LIRI-JP8124518789124518789single base substitutionGTmissense_variantT226N677C>A
LIRI-JP8124521194124521194single base substitutionAGdownstream_gene_variant
LIRI-JP8124521194124521194single base substitutionAGintron_variant
LIRI-JP8124521194124521194single base substitutionAGupstream_gene_variant
LIRI-JP8124523483124523483single base substitutionGAdownstream_gene_variant
LIRI-JP8124523483124523483single base substitutionGAintron_variant
LIRI-JP8124523483124523483single base substitutionGAupstream_gene_variant
LIRI-JP8124524953124524953single base substitutionACdownstream_gene_variant
LIRI-JP8124524953124524953single base substitutionACintron_variant
LIRI-JP8124529571124529571single base substitutionACintron_variant
LIRI-JP8124530539124530539single base substitutionAGintron_variant
LIRI-JP8124535372124535372single base substitutionGAdownstream_gene_variant
LIRI-JP8124535372124535372single base substitutionGAintron_variant
LIRI-JP8124536642124536642single base substitutionACdownstream_gene_variant
LIRI-JP8124536642124536642single base substitutionACintron_variant
LIRI-JP8124538839124538839single base substitutionACdownstream_gene_variant
LIRI-JP8124538839124538839single base substitutionACintron_variant
LIRI-JP8124538890124538890single base substitutionAGdownstream_gene_variant
LIRI-JP8124538890124538890single base substitutionAGintron_variant
LIRI-JP8124541311124541311single base substitutionCTintron_variant
LIRI-JP8124544420124544420single base substitutionCGintron_variant
LIRI-JP8124544420124544420single base substitutionCGupstream_gene_variant
LIRI-JP8124548396124548396single base substitutionCAintron_variant
LIRI-JP8124548396124548396single base substitutionCAupstream_gene_variant
LIRI-JP8124548525124548525single base substitutionAGintron_variant
LIRI-JP8124548525124548525single base substitutionAGupstream_gene_variant
LIRI-JP8124552850124552850insertion of <=200bp-GGACintron_variant
LIRI-JP8124554087124554087single base substitutionCTupstream_gene_variant
LIRI-JP8124554620124554620single base substitutionCTupstream_gene_variant
LIRI-JP8124554950124554950single base substitutionTCupstream_gene_variant
LIRI-JP8124555264124555264single base substitutionAGupstream_gene_variant
LIRI-JP8124555391124555391single base substitutionCTupstream_gene_variant
LUSC-KR8124510371124510371single base substitutionTC3_prime_UTR_variant
LUSC-KR8124510371124510371single base substitutionTCdownstream_gene_variant
LUSC-KR8124517208124517208single base substitutionCAintron_variant
LUSC-KR8124525377124525377single base substitutionTGdownstream_gene_variant
LUSC-KR8124525377124525377single base substitutionTGintron_variant
LUSC-KR8124525483124525483single base substitutionCTdownstream_gene_variant
LUSC-KR8124525483124525483single base substitutionCTexon_variant
LUSC-KR8124525483124525483single base substitutionCTintron_variant
LUSC-KR8124525483124525483single base substitutionCTsynonymous_variantT202T606G>A
LUSC-KR8124526763124526763single base substitutionTCintron_variant
LUSC-KR8124552189124552189single base substitutionGCintron_variant
LUSC-KR8124552473124552473single base substitutionGCintron_variant
LUSC-US8124512380124512380deletion of <=200bpT-3_prime_UTR_variant
LUSC-US8124512380124512380deletion of <=200bpT-downstream_gene_variant
LUSC-US8124546943124546943single base substitutionCAmissense_variantQ76H228G>T
LUSC-US8124546943124546943single base substitutionCAsplice_region_variant
LUSC-US8124546943124546943single base substitutionCAupstream_gene_variant
LUSC-US8124547001124547001single base substitutionTCexon_variant
LUSC-US8124547001124547001single base substitutionTCmissense_variantY57C170A>G
LUSC-US8124547001124547001single base substitutionTCupstream_gene_variant
LUSC-US8124553144124553144single base substitutionGAexon_variant
LUSC-US8124553144124553144single base substitutionGAsynonymous_variantL37L111C>T
LUSC-US8124553156124553156single base substitutionGAexon_variant
LUSC-US8124553156124553156single base substitutionGAsynonymous_variantF33F99C>T
MALY-DE8124507892124507892insertion of <=200bp-Gdownstream_gene_variant
MALY-DE8124518619124518619single base substitutionGAintron_variant
MALY-DE8124525646124525646single base substitutionATintron_variant
MALY-DE8124526755124526755single base substitutionCGintron_variant
MALY-DE8124531568124531568single base substitutionCTintron_variant
MALY-DE8124543619124543619single base substitutionTCintron_variant
MALY-DE8124545092124545092single base substitutionACintron_variant
MALY-DE8124545092124545092single base substitutionACupstream_gene_variant
MALY-DE8124548188124548188single base substitutionTCintron_variant
MALY-DE8124548188124548188single base substitutionTCupstream_gene_variant
MELA-AU8124505242124505242single base substitutionCTdownstream_gene_variant
MELA-AU8124505311124505311single base substitutionCTdownstream_gene_variant
MELA-AU8124505340124505340single base substitutionCTdownstream_gene_variant
MELA-AU8124505366124505366single base substitutionCAdownstream_gene_variant
MELA-AU8124505802124505802single base substitutionCTdownstream_gene_variant
MELA-AU8124505932124505932single base substitutionCTdownstream_gene_variant
MELA-AU8124506209124506209single base substitutionCTdownstream_gene_variant
MELA-AU8124506939124506939single base substitutionGAdownstream_gene_variant
MELA-AU8124507329124507329single base substitutionGAdownstream_gene_variant
MELA-AU8124507586124507586single base substitutionATdownstream_gene_variant
MELA-AU8124507977124507977single base substitutionCAdownstream_gene_variant
MELA-AU8124508086124508086single base substitutionCTdownstream_gene_variant
MELA-AU8124508784124508784single base substitutionCTdownstream_gene_variant
MELA-AU8124508926124508926single base substitutionCTdownstream_gene_variant
MELA-AU8124509031124509031single base substitutionCTdownstream_gene_variant
MELA-AU8124509360124509360single base substitutionCTdownstream_gene_variant
MELA-AU8124510355124510355single base substitutionCT3_prime_UTR_variant
MELA-AU8124510355124510355single base substitutionCTdownstream_gene_variant
MELA-AU8124510390124510390single base substitutionGA3_prime_UTR_variant
MELA-AU8124510390124510390single base substitutionGAdownstream_gene_variant
MELA-AU8124510647124510648multiple base substitution (>=2bp and <=200bp)GGAA3_prime_UTR_variant
MELA-AU8124510647124510648multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU8124510771124510771single base substitutionGA3_prime_UTR_variant
MELA-AU8124510771124510771single base substitutionGAdownstream_gene_variant
MELA-AU8124511462124511462single base substitutionGA3_prime_UTR_variant
MELA-AU8124511462124511462single base substitutionGAdownstream_gene_variant
MELA-AU8124511755124511782deletion of <=200bpAGTTAAAAAAATTCACACATAAAATTAC-3_prime_UTR_variant
MELA-AU8124511755124511782deletion of <=200bpAGTTAAAAAAATTCACACATAAAATTAC-downstream_gene_variant
MELA-AU8124512057124512057single base substitutionGA3_prime_UTR_variant
MELA-AU8124512057124512057single base substitutionGAdownstream_gene_variant
MELA-AU8124512476124512476single base substitutionGA3_prime_UTR_variant
MELA-AU8124512476124512476single base substitutionGAdownstream_gene_variant
MELA-AU8124513492124513492single base substitutionGA3_prime_UTR_variant
MELA-AU8124513492124513492single base substitutionGAdownstream_gene_variant
MELA-AU8124513590124513590single base substitutionGA3_prime_UTR_variant
MELA-AU8124513590124513590single base substitutionGAdownstream_gene_variant
MELA-AU8124513629124513629single base substitutionCA3_prime_UTR_variant
MELA-AU8124513629124513629single base substitutionCAdownstream_gene_variant
MELA-AU8124513841124513841single base substitutionCT3_prime_UTR_variant
MELA-AU8124513841124513841single base substitutionCTdownstream_gene_variant
MELA-AU8124513954124513954single base substitutionTA3_prime_UTR_variant
MELA-AU8124513954124513954single base substitutionTAdownstream_gene_variant
MELA-AU8124515099124515099single base substitutionGA3_prime_UTR_variant
MELA-AU8124515099124515099single base substitutionGAdownstream_gene_variant
MELA-AU8124515223124515223single base substitutionAG3_prime_UTR_variant
MELA-AU8124515223124515223single base substitutionAGdownstream_gene_variant
MELA-AU8124515581124515581single base substitutionGA3_prime_UTR_variant
MELA-AU8124515581124515581single base substitutionGAexon_variant
MELA-AU8124516212124516212single base substitutionGAintron_variant
MELA-AU8124516960124516960single base substitutionTGexon_variant
MELA-AU8124516960124516960single base substitutionTGmissense_variantK195Q583A>C
MELA-AU8124516960124516960single base substitutionTGmissense_variantK288Q862A>C
MELA-AU8124519254124519254single base substitutionACintron_variant
MELA-AU8124519254124519254single base substitutionACupstream_gene_variant
MELA-AU8124520374124520374single base substitutionGAintron_variant
MELA-AU8124520374124520374single base substitutionGAupstream_gene_variant
MELA-AU8124520376124520376single base substitutionGAintron_variant
MELA-AU8124520376124520376single base substitutionGAupstream_gene_variant
MELA-AU8124520678124520678single base substitutionGAdownstream_gene_variant
MELA-AU8124520678124520678single base substitutionGAintron_variant
MELA-AU8124520678124520678single base substitutionGAupstream_gene_variant
MELA-AU8124520771124520771single base substitutionGAdownstream_gene_variant
MELA-AU8124520771124520771single base substitutionGAintron_variant
MELA-AU8124520771124520771single base substitutionGAupstream_gene_variant
MELA-AU8124521181124521181single base substitutionCAdownstream_gene_variant
MELA-AU8124521181124521181single base substitutionCAintron_variant
MELA-AU8124521181124521181single base substitutionCAupstream_gene_variant
MELA-AU8124521217124521217single base substitutionCGdownstream_gene_variant
MELA-AU8124521217124521217single base substitutionCGintron_variant
MELA-AU8124521217124521217single base substitutionCGupstream_gene_variant
MELA-AU8124522649124522649single base substitutionCTdownstream_gene_variant
MELA-AU8124522649124522649single base substitutionCTintron_variant
MELA-AU8124522649124522649single base substitutionCTupstream_gene_variant
MELA-AU8124523968124523968single base substitutionGAdownstream_gene_variant
MELA-AU8124523968124523968single base substitutionGAintron_variant
MELA-AU8124525973124525973single base substitutionGAintron_variant
MELA-AU8124526119124526119single base substitutionGAintron_variant
MELA-AU8124526602124526602single base substitutionTAintron_variant
MELA-AU8124526826124526826single base substitutionTAintron_variant
MELA-AU8124526828124526828single base substitutionAGintron_variant
MELA-AU8124527936124527936single base substitutionTAintron_variant
MELA-AU8124528665124528665single base substitutionGAintron_variant
MELA-AU8124529793124529793single base substitutionCTintron_variant
MELA-AU8124530153124530154multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU8124530858124530858single base substitutionGAintron_variant
MELA-AU8124531448124531448single base substitutionGAintron_variant
MELA-AU8124531578124531578single base substitutionGAintron_variant
MELA-AU8124531962124531962single base substitutionGAintron_variant
MELA-AU8124532240124532240single base substitutionTCintron_variant
MELA-AU8124532270124532270single base substitutionTCintron_variant
MELA-AU8124532400124532400single base substitutionGTintron_variant
MELA-AU8124532595124532595single base substitutionCTintron_variant
MELA-AU8124533007124533007single base substitutionATintron_variant
MELA-AU8124533441124533441single base substitutionCTintron_variant
MELA-AU8124533668124533668single base substitutionGAintron_variant
MELA-AU8124533783124533783single base substitutionGAintron_variant
MELA-AU8124534614124534614single base substitutionGAdownstream_gene_variant
MELA-AU8124534614124534614single base substitutionGAintron_variant
MELA-AU8124534663124534663single base substitutionGAdownstream_gene_variant
MELA-AU8124534663124534663single base substitutionGAintron_variant
MELA-AU8124534719124534719single base substitutionGAdownstream_gene_variant
MELA-AU8124534719124534719single base substitutionGAintron_variant
MELA-AU8124534944124534944single base substitutionCTdownstream_gene_variant
MELA-AU8124534944124534944single base substitutionCTintron_variant
MELA-AU8124535036124535036single base substitutionGAdownstream_gene_variant
MELA-AU8124535036124535036single base substitutionGAintron_variant
MELA-AU8124535397124535397single base substitutionATdownstream_gene_variant
MELA-AU8124535397124535397single base substitutionATintron_variant
MELA-AU8124536369124536369single base substitutionGAdownstream_gene_variant
MELA-AU8124536369124536369single base substitutionGAintron_variant
MELA-AU8124536673124536673single base substitutionCTdownstream_gene_variant
MELA-AU8124536673124536673single base substitutionCTintron_variant
MELA-AU8124536688124536688single base substitutionCGdownstream_gene_variant
MELA-AU8124536688124536688single base substitutionCGintron_variant
MELA-AU8124536933124536933single base substitutionTCdownstream_gene_variant
MELA-AU8124536933124536933single base substitutionTCintron_variant
MELA-AU8124537028124537028single base substitutionGAdownstream_gene_variant
MELA-AU8124537028124537028single base substitutionGAintron_variant
MELA-AU8124538137124538137single base substitutionGAdownstream_gene_variant
MELA-AU8124538137124538137single base substitutionGAintron_variant
MELA-AU8124538610124538610single base substitutionGAdownstream_gene_variant
MELA-AU8124538610124538610single base substitutionGAintron_variant
MELA-AU8124539154124539157deletion of <=200bpCAAG-downstream_gene_variant
MELA-AU8124539154124539157deletion of <=200bpCAAG-intron_variant
MELA-AU8124539245124539245single base substitutionCTexon_variant
MELA-AU8124539245124539245single base substitutionCTintron_variant
MELA-AU8124540367124540367single base substitutionACintron_variant
MELA-AU8124540430124540430single base substitutionGAintron_variant
MELA-AU8124541318124541318single base substitutionACintron_variant
MELA-AU8124541476124541476single base substitutionTCintron_variant
MELA-AU8124541526124541526single base substitutionAGintron_variant
MELA-AU8124542285124542285single base substitutionGAintron_variant
MELA-AU8124543268124543268single base substitutionGAintron_variant
MELA-AU8124543518124543518single base substitutionGAintron_variant
MELA-AU8124543691124543691single base substitutionGAintron_variant
MELA-AU8124543828124543828single base substitutionCTintron_variant
MELA-AU8124544065124544065single base substitutionCTintron_variant
MELA-AU8124544528124544528single base substitutionATintron_variant
MELA-AU8124544528124544528single base substitutionATupstream_gene_variant
MELA-AU8124544625124544625single base substitutionATintron_variant
MELA-AU8124544625124544625single base substitutionATupstream_gene_variant
MELA-AU8124544714124544714single base substitutionGAintron_variant
MELA-AU8124544714124544714single base substitutionGAupstream_gene_variant
MELA-AU8124544874124544874single base substitutionCTintron_variant
MELA-AU8124544874124544874single base substitutionCTupstream_gene_variant
MELA-AU8124545383124545383single base substitutionGAintron_variant
MELA-AU8124545383124545383single base substitutionGAupstream_gene_variant
MELA-AU8124545839124545839single base substitutionGAintron_variant
MELA-AU8124545839124545839single base substitutionGAupstream_gene_variant
MELA-AU8124546035124546035single base substitutionGAintron_variant
MELA-AU8124546035124546035single base substitutionGAupstream_gene_variant
MELA-AU8124548233124548233single base substitutionGAintron_variant
MELA-AU8124548233124548233single base substitutionGAupstream_gene_variant
MELA-AU8124548724124548724single base substitutionCTintron_variant
MELA-AU8124548724124548724single base substitutionCTupstream_gene_variant
MELA-AU8124549549124549549single base substitutionACintron_variant
MELA-AU8124549771124549771single base substitutionTCintron_variant
MELA-AU8124550711124550716deletion of <=200bpCCTGTG-intron_variant
MELA-AU8124551184124551184deletion of <=200bpA-intron_variant
MELA-AU8124551354124551354single base substitutionTGintron_variant
MELA-AU8124552509124552509single base substitutionCTintron_variant
MELA-AU8124552525124552525single base substitutionGAintron_variant
MELA-AU8124553028124553028single base substitutionCAintron_variant
MELA-AU8124553509124553509single base substitutionGAupstream_gene_variant
MELA-AU8124553527124553527single base substitutionCTupstream_gene_variant
MELA-AU8124553564124553564single base substitutionTCupstream_gene_variant
MELA-AU8124554997124554997single base substitutionCTupstream_gene_variant
MELA-AU8124555430124555430single base substitutionGAupstream_gene_variant
MELA-AU8124555461124555461single base substitutionGCupstream_gene_variant
MELA-AU8124556002124556002single base substitutionCTupstream_gene_variant
MELA-AU8124556311124556311single base substitutionGAupstream_gene_variant
MELA-AU8124557364124557364single base substitutionGAupstream_gene_variant
MELA-AU8124557376124557376single base substitutionGAupstream_gene_variant
MELA-AU8124557400124557400single base substitutionCTupstream_gene_variant
MELA-AU8124557534124557534single base substitutionAGupstream_gene_variant
MELA-AU8124557629124557629single base substitutionGAupstream_gene_variant
MELA-AU8124557662124557662single base substitutionGCupstream_gene_variant
MELA-AU8124557663124557663single base substitutionTAupstream_gene_variant
MELA-AU8124557817124557817single base substitutionCTupstream_gene_variant
MELA-AU8124557842124557842single base substitutionGAupstream_gene_variant
MELA-AU8124558050124558050single base substitutionCTupstream_gene_variant
MELA-AU8124558134124558134single base substitutionTCupstream_gene_variant
MELA-AU8124558442124558442single base substitutionGAupstream_gene_variant
ORCA-IN8124551715124551715single base substitutionGAintron_variant
ORCA-IN8124558271124558271single base substitutionGAupstream_gene_variant
OV-AU8124514897124514897single base substitutionGC3_prime_UTR_variant
OV-AU8124514897124514897single base substitutionGCdownstream_gene_variant
OV-AU8124521075124521075single base substitutionAGdownstream_gene_variant
OV-AU8124521075124521075single base substitutionAGintron_variant
OV-AU8124521075124521075single base substitutionAGupstream_gene_variant
OV-AU8124530207124530207single base substitutionGCintron_variant
OV-AU8124535224124535224single base substitutionAGdownstream_gene_variant
OV-AU8124535224124535224single base substitutionAGintron_variant
OV-AU8124535751124535751single base substitutionATdownstream_gene_variant
OV-AU8124535751124535751single base substitutionATintron_variant
OV-AU8124541899124541899single base substitutionACintron_variant
OV-AU8124545088124545088single base substitutionTCintron_variant
OV-AU8124545088124545088single base substitutionTCupstream_gene_variant
OV-AU8124548812124548812single base substitutionCGintron_variant
OV-AU8124548812124548812single base substitutionCGupstream_gene_variant
OV-AU8124551008124551008single base substitutionGAintron_variant
OV-AU8124553220124553220single base substitutionCAexon_variant
OV-AU8124553220124553220single base substitutionCAmissense_variantG12V35G>T
OV-AU8124553453124553453single base substitutionCTupstream_gene_variant
OV-AU8124553884124553884single base substitutionGAupstream_gene_variant
OV-AU8124555791124555791single base substitutionCGupstream_gene_variant
OV-AU8124556238124556238single base substitutionCGupstream_gene_variant
PACA-AU8124506547124506547single base substitutionGAdownstream_gene_variant
PACA-AU8124508443124508443deletion of <=200bpA-downstream_gene_variant
PACA-AU8124509057124509057single base substitutionTAdownstream_gene_variant
PACA-AU8124512047124512047single base substitutionCT3_prime_UTR_variant
PACA-AU8124512047124512047single base substitutionCTdownstream_gene_variant
PACA-AU8124518636124518636single base substitutionCTexon_variant
PACA-AU8124518636124518636single base substitutionCTmissense_variantR184Q551G>A
PACA-AU8124518636124518636single base substitutionCTmissense_variantR277Q830G>A
PACA-AU8124520446124520446single base substitutionTAintron_variant
PACA-AU8124520446124520446single base substitutionTAupstream_gene_variant
PACA-AU8124523721124523721single base substitutionTGdownstream_gene_variant
PACA-AU8124523721124523721single base substitutionTGintron_variant
PACA-AU8124523721124523721single base substitutionTGupstream_gene_variant
PACA-AU8124529285124529285single base substitutionAGintron_variant
PACA-AU8124533885124533885single base substitutionTAintron_variant
PACA-AU8124534347124534347single base substitutionGAdownstream_gene_variant
PACA-AU8124534347124534347single base substitutionGAintron_variant
PACA-AU8124535878124535878single base substitutionACdownstream_gene_variant
PACA-AU8124535878124535878single base substitutionACintron_variant
PACA-AU8124536697124536697single base substitutionGCdownstream_gene_variant
PACA-AU8124536697124536697single base substitutionGCintron_variant
PACA-AU8124538397124538397single base substitutionATdownstream_gene_variant
PACA-AU8124538397124538397single base substitutionATintron_variant
PACA-AU8124538627124538627single base substitutionTCdownstream_gene_variant
PACA-AU8124538627124538627single base substitutionTCintron_variant
PACA-AU8124538681124538681single base substitutionGTdownstream_gene_variant
PACA-AU8124538681124538681single base substitutionGTintron_variant
PACA-AU8124540876124540881deletion of <=200bpAGTTAT-intron_variant
PACA-AU8124541283124541283single base substitutionGAintron_variant
PACA-AU8124548064124548064deletion of <=200bpG-intron_variant
PACA-AU8124548064124548064deletion of <=200bpG-upstream_gene_variant
PACA-AU8124549049124549049single base substitutionGCintron_variant
PACA-AU8124549049124549049single base substitutionGCupstream_gene_variant
PACA-AU8124549667124549667single base substitutionACintron_variant
PACA-AU8124550636124550637deletion of <=200bpTC-intron_variant
PACA-AU8124552130124552130single base substitutionGTintron_variant
PACA-CA8124506970124506970single base substitutionATdownstream_gene_variant
PACA-CA8124507126124507126single base substitutionTGdownstream_gene_variant
PACA-CA8124507854124507854single base substitutionTCdownstream_gene_variant
PACA-CA8124507886124507886single base substitutionGAdownstream_gene_variant
PACA-CA8124509628124509628single base substitutionCAdownstream_gene_variant
PACA-CA8124510190124510190single base substitutionCT3_prime_UTR_variant
PACA-CA8124511405124511405single base substitutionCG3_prime_UTR_variant
PACA-CA8124511405124511405single base substitutionCGdownstream_gene_variant
PACA-CA8124518840124518840insertion of <=200bp-Gexon_variant
PACA-CA8124518840124518840insertion of <=200bp-Gintron_variant
PACA-CA8124521761124521761single base substitutionGAdownstream_gene_variant
PACA-CA8124521761124521761single base substitutionGAintron_variant
PACA-CA8124521761124521761single base substitutionGAupstream_gene_variant
PACA-CA8124522438124522438single base substitutionCGdownstream_gene_variant
PACA-CA8124522438124522438single base substitutionCGintron_variant
PACA-CA8124522438124522438single base substitutionCGupstream_gene_variant
PACA-CA8124523167124523167single base substitutionTCdownstream_gene_variant
PACA-CA8124523167124523167single base substitutionTCintron_variant
PACA-CA8124523167124523167single base substitutionTCupstream_gene_variant
PACA-CA8124531974124531974deletion of <=200bpT-intron_variant
PACA-CA8124533343124533343single base substitutionTCintron_variant
PACA-CA8124537050124537050single base substitutionGAdownstream_gene_variant
PACA-CA8124537050124537050single base substitutionGAintron_variant
PACA-CA8124538013124538013single base substitutionACdownstream_gene_variant
PACA-CA8124538013124538013single base substitutionACintron_variant
PACA-CA8124541558124541558single base substitutionAGintron_variant
PACA-CA8124549513124549513single base substitutionATintron_variant
PACA-CA8124552160124552160single base substitutionGCintron_variant
PACA-CA8124553094124553094single base substitutionGAintron_variant
PACA-CA8124557115124557115single base substitutionTCupstream_gene_variant
PACA-CA8124558195124558195single base substitutionCTupstream_gene_variant
PAEN-AU8124547206124547206single base substitutionGAintron_variant
PAEN-AU8124547206124547206single base substitutionGAupstream_gene_variant
PAEN-IT8124537185124537185single base substitutionCAdownstream_gene_variant
PAEN-IT8124537185124537185single base substitutionCAintron_variant
PAEN-IT8124544936124544936single base substitutionCAintron_variant
PAEN-IT8124544936124544936single base substitutionCAupstream_gene_variant
PBCA-DE8124510532124510532single base substitutionCT3_prime_UTR_variant
PBCA-DE8124510532124510532single base substitutionCTdownstream_gene_variant
PBCA-DE8124512360124512360single base substitutionTC3_prime_UTR_variant
PBCA-DE8124512360124512360single base substitutionTCdownstream_gene_variant
PBCA-DE8124528459124528459single base substitutionGTintron_variant
PBCA-DE8124547489124547489deletion of <=200bpA-intron_variant
PBCA-DE8124547489124547489deletion of <=200bpA-upstream_gene_variant
PBCA-DE8124549809124549809single base substitutionGAintron_variant
PRAD-CA8124544605124544605single base substitutionGAintron_variant
PRAD-CA8124544605124544605single base substitutionGAupstream_gene_variant
PRAD-UK8124531749124531749single base substitutionCAintron_variant
PRAD-UK8124534936124534936single base substitutionCGdownstream_gene_variant
PRAD-UK8124534936124534936single base substitutionCGintron_variant
PRAD-UK8124541814124541814single base substitutionCGintron_variant
PRAD-UK8124553498124553498single base substitutionTAupstream_gene_variant
READ-US8124515620124515620single base substitutionTGexon_variant
READ-US8124515620124515620single base substitutionTGmissense_variantK261T782A>C
READ-US8124515620124515620single base substitutionTGmissense_variantK354T1061A>C
RECA-EU8124524629124524629single base substitutionAGdownstream_gene_variant
RECA-EU8124524629124524629single base substitutionAGintron_variant
RECA-EU8124530381124530381single base substitutionTAintron_variant
RECA-EU8124532180124532180single base substitutionACintron_variant
RECA-EU8124556127124556127single base substitutionCTupstream_gene_variant
SKCA-BR8124506043124506043single base substitutionGAdownstream_gene_variant
SKCA-BR8124506412124506412insertion of <=200bp-CAdownstream_gene_variant
SKCA-BR8124508149124508149single base substitutionGAdownstream_gene_variant
SKCA-BR8124508965124508965single base substitutionTAdownstream_gene_variant
SKCA-BR8124513604124513604insertion of <=200bp-AAAAAAAAAAC3_prime_UTR_variant
SKCA-BR8124513604124513604insertion of <=200bp-AAAAAAAAAACdownstream_gene_variant
SKCA-BR8124519678124519678insertion of <=200bp-GGGGTGTGTGTGTGTintron_variant
SKCA-BR8124519678124519678insertion of <=200bp-GGGGTGTGTGTGTGTupstream_gene_variant
SKCA-BR8124525483124525483single base substitutionCTdownstream_gene_variant
SKCA-BR8124525483124525483single base substitutionCTexon_variant
SKCA-BR8124525483124525483single base substitutionCTintron_variant
SKCA-BR8124525483124525483single base substitutionCTsynonymous_variantT202T606G>A
SKCA-BR8124526607124526607single base substitutionGAintron_variant
SKCA-BR8124529657124529657single base substitutionGAintron_variant
SKCA-BR8124530929124530929single base substitutionAGintron_variant
SKCA-BR8124532562124532562single base substitutionAGintron_variant
SKCA-BR8124532572124532572single base substitutionAGintron_variant
SKCA-BR8124535860124535867deletion of <=200bpCAACAACA-downstream_gene_variant
SKCA-BR8124535860124535867deletion of <=200bpCAACAACA-intron_variant
SKCA-BR8124536947124536947single base substitutionGAdownstream_gene_variant
SKCA-BR8124536947124536947single base substitutionGAintron_variant
SKCA-BR8124537894124537894single base substitutionCTdownstream_gene_variant
SKCA-BR8124537894124537894single base substitutionCTintron_variant
SKCA-BR8124537897124537897single base substitutionGAdownstream_gene_variant
SKCA-BR8124537897124537897single base substitutionGAintron_variant
SKCA-BR8124539494124539494single base substitutionCGintron_variant
SKCA-BR8124539494124539494single base substitutionCGsplice_region_variant
SKCA-BR8124543506124543506single base substitutionGCintron_variant
SKCA-BR8124553085124553085single base substitutionGAintron_variant
SKCA-BR8124553663124553663single base substitutionACupstream_gene_variant
SKCA-BR8124555624124555624single base substitutionGAupstream_gene_variant
SKCA-BR8124557629124557629single base substitutionGAupstream_gene_variant
SKCA-BR8124558050124558050single base substitutionCTupstream_gene_variant
SKCM-US8124518738124518738single base substitutionCTexon_variant
SKCM-US8124518738124518738single base substitutionCTmissense_variantG150E449G>A
SKCM-US8124518738124518738single base substitutionCTmissense_variantG243E728G>A
SKCM-US8124518793124518793single base substitutionAGexon_variant
SKCM-US8124518793124518793single base substitutionAGmissense_variantF132L394T>C
SKCM-US8124518793124518793single base substitutionAGmissense_variantF225L673T>C
SKCM-US8124518802124518802single base substitutionCTexon_variant
SKCM-US8124518802124518802single base substitutionCTmissense_variantG129S385G>A
SKCM-US8124518802124518802single base substitutionCTmissense_variantG222S664G>A
SKCM-US8124553147124553147single base substitutionGAexon_variant
SKCM-US8124553147124553147single base substitutionGAsynonymous_variantD36D108C>T
SKCM-US8124553243124553243single base substitutionGAexon_variant
SKCM-US8124553243124553243single base substitutionGAsynonymous_variantL4L12C>T
SKCM-US8124553245124553245single base substitutionGAexon_variant
SKCM-US8124553245124553245single base substitutionGAmissense_variantL4F10C>T
STAD-US8124515635124515635single base substitutionAGexon_variant
STAD-US8124515635124515635single base substitutionAGmissense_variantF256S767T>C
STAD-US8124515635124515635single base substitutionAGmissense_variantF349S1046T>C
STAD-US8124516885124516885single base substitutionTCexon_variant
STAD-US8124516885124516885single base substitutionTCmissense_variantT220A658A>G
STAD-US8124516885124516885single base substitutionTCmissense_variantT313A937A>G
STAD-US8124526525124526525single base substitutionCTexon_variant
STAD-US8124526525124526525single base substitutionCTintron_variant
STAD-US8124526525124526525single base substitutionCTmissense_variantA141T421G>A
STAD-US8124544137124544137single base substitutionCAsplice_donor_variant
STAD-US8124544175124544175single base substitutionGAexon_variant
STAD-US8124544175124544175single base substitutionGAmissense_variantA112V335C>T
STAD-US8124546990124546990single base substitutionCTexon_variant
STAD-US8124546990124546990single base substitutionCTmissense_variantA61T181G>A
STAD-US8124546990124546990single base substitutionCTupstream_gene_variant
THCA-SA8124518694124518694single base substitutionCTexon_variant
THCA-SA8124518694124518694single base substitutionCTmissense_variantV165M493G>A
THCA-SA8124518694124518694single base substitutionCTmissense_variantV258M772G>A
UCEC-US8124525447124525447single base substitutionCAdownstream_gene_variant
UCEC-US8124525447124525447single base substitutionCAexon_variant
UCEC-US8124525447124525447single base substitutionCAintron_variant
UCEC-US8124525447124525447single base substitutionCAmissense_variantQ214H642G>T
UCEC-US8124525496124525496single base substitutionTCdownstream_gene_variant
UCEC-US8124525496124525496single base substitutionTCexon_variant
UCEC-US8124525496124525496single base substitutionTCintron_variant
UCEC-US8124525496124525496single base substitutionTCmissense_variantY198C593A>G
UCEC-US8124525623124525623single base substitutionCTintron_variant
UCEC-US8124525623124525623single base substitutionCTsplice_acceptor_variant
UCEC-US8124526528124526528single base substitutionTCexon_variant
UCEC-US8124526528124526528single base substitutionTCintron_variant
UCEC-US8124526528124526528single base substitutionTCmissense_variantI140V418A>G
UCEC-US8124526529124526529single base substitutionGAexon_variant
UCEC-US8124526529124526529single base substitutionGAintron_variant
UCEC-US8124526529124526529single base substitutionGAsynonymous_variantG139G417C>T
UCEC-US8124526531124526531single base substitutionCTexon_variant
UCEC-US8124526531124526531single base substitutionCTintron_variant
UCEC-US8124526531124526531single base substitutionCTmissense_variantG139S415G>A
UCEC-US8124544230124544230single base substitutionGAexon_variant
UCEC-US8124544230124544230single base substitutionGAmissense_variantR94C280C>T
UCEC-US8124544230124544230single base substitutionGAsplice_region_variant
UCEC-US8124547024124547024single base substitutionCAexon_variant
UCEC-US8124547024124547024single base substitutionCAmissense_variantE49D147G>T
UCEC-US8124547024124547024single base substitutionCAupstream_gene_variant
UCEC-US8124547051124547051single base substitutionGTexon_variant
UCEC-US8124547051124547051single base substitutionGTstop_gainedY40*120C>A
UCEC-US8124547051124547051single base substitutionGTupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-AP-A059-01COSM1095782c.593A>Gp.Y198CSubstitution - Missense8:123513256-123513256-
TCGA-22-5473-01COSM749478c.170A>Gp.Y57CSubstitution - Missense8:123534761-123534761-
T3724COSM4683978c.210T>Cp.N70NSubstitution - coding silent8:123534721-123534721-
587222COSM1206828c.429G>Tp.K143NSubstitution - Missense8:123514277-123514277-
TCGA-EE-A3JD-06COSM4393947c.12C>Tp.L4LSubstitution - coding silent8:123541003-123541003-
ESCC_BICR_028TCOSM5431852c.27G>Ap.R9RSubstitution - coding silent8:123540988-123540988-
TCGA-F5-6814-01COSM3432092c.1061A>Cp.K354TSubstitution - Missense8:123503380-123503380-
CRC-19TCOSM5482156c.753G>Cp.Q251HSubstitution - Missense8:123506473-123506473-
TCGA-B6-A0I1-01COSM3833999c.741C>Ap.V247VSubstitution - coding silent8:123506485-123506485-
TCGA-D3-A2JL-06COSM3644835c.728G>Ap.G243ESubstitution - Missense8:123506498-123506498-
TCGA-33-4583-01COSM749477c.111C>Tp.L37LSubstitution - coding silent8:123540904-123540904-
CSCC-31-TCOSM4507900c.75C>Tp.F25FSubstitution - coding silent8:123540940-123540940-
TCGA-B5-A0JY-01COSM1095788c.147G>Tp.E49DSubstitution - Missense8:123534784-123534784-
GC1_TCOSM150535c.730C>Tp.R244WSubstitution - Missense8:123506496-123506496-
TCGA-ER-A19N-06COSM3644837c.664G>Ap.G222SSubstitution - Missense8:123506562-123506562-
TCGA-AP-A051-01COSM1095783c.467-1G>Ap.?Unknown8:123513383-123513383-
TCGA-AX-A064-01COSM1095784c.418A>Gp.I140VSubstitution - Missense8:123514288-123514288-
TCGA-BR-8487-01COSM3896568c.1046T>Cp.F349SSubstitution - Missense8:123503395-123503395-
TCGA-AP-A051-01COSM1095781c.642G>Tp.Q214HSubstitution - Missense8:123513207-123513207-
TCGA-CA-6717-01COSM1454669c.246_247insAp.W83fs*10Insertion - Frameshift8:123533223-123533224-
TCGA-BR-6452-01COSM3896571c.372+1G>Tp.?Unknown8:123531897-123531897-
T11COSM5617778c.733G>Ap.D245NSubstitution - Missense8:123506493-123506493-
TCGA-D8-A1JC-01COSM1488980c.390A>Gp.A130ASubstitution - coding silent8:123514316-123514316-
ESCC_113COSM5639617c.786C>Tp.D262DSubstitution - coding silent8:123506440-123506440-
B85-0COSM1755553c.324C>Tp.D108DSubstitution - coding silent8:123531946-123531946-
TCGA-EE-A3JD-06COSM4396666c.10C>Tp.L4FSubstitution - Missense8:123541005-123541005-
TCGA-AM-5820-01COSM3763036c.552C>Tp.V184VSubstitution - coding silent8:123513297-123513297-
TCGA-85-6561-01COSM749479c.228G>Tp.Q76HSubstitution - Missense8:123534703-123534703-
AOCS-104-1-6COSM4150513c.35G>Tp.G12VSubstitution - Missense8:123540980-123540980-
TCGA-DK-A3X1-01COSM3778875c.934G>Cp.D312HSubstitution - Missense8:123504648-123504648-
I2L-P7-Tumor-OrganoidCOSM5358975c.299T>Cp.L100PSubstitution - Missense8:123531971-123531971-
N194TCOSM236106c.980G>Tp.G327VSubstitution - Missense8:123503461-123503461-
T1154COSM4683979c.178G>Ap.A60TSubstitution - Missense8:123534753-123534753-
HOP-92COSM1674154c.927G>Cp.Q309HSubstitution - Missense8:123504655-123504655-
PD14468aCOSM5767851c.45G>Tp.W15CSubstitution - Missense8:123540970-123540970-
LUAD-S01331COSM396634c.763G>Tp.D255YSubstitution - Missense8:123506463-123506463-
3N30-VS-3T30COSM4980585c.1023C>Tp.S341SSubstitution - coding silent8:123503418-123503418-
SNUH_G26_S1COSM3982384c.606G>Ap.T202TSubstitution - coding silent8:123513243-123513243-
8069192COSM4408271c.830G>Ap.R277QSubstitution - Missense8:123506396-123506396-
228COSM4426150c.342G>Cp.L114LSubstitution - coding silent8:123531928-123531928-
B54-TumorCOSM1755554c.84G>Cp.E28DSubstitution - Missense8:123540931-123540931-
TCGA-AP-A0LM-01COSM1095786c.415G>Ap.G139SSubstitution - Missense8:123514291-123514291-
TCGA-37-3783-01COSM749476c.99C>Tp.F33FSubstitution - coding silent8:123540916-123540916-
ESCC_54COSM5631596c.266G>Cp.G89ASubstitution - Missense8:123533204-123533204-
C086COSM5531112c.9C>Tp.F3FSubstitution - coding silent8:123541006-123541006-
TCGA-BR-8680-01COSM3896572c.181G>Ap.A61TSubstitution - Missense8:123534750-123534750-
12TCOSM108654c.407C>Tp.S136FSubstitution - Missense8:123514299-123514299-
TCGA-AA-3966-01COSM272686c.364G>Ap.V122MSubstitution - Missense8:123531906-123531906-
112313COSM95883c.102G>Ap.V34VSubstitution - coding silent8:123540913-123540913-
U251COSM1674154c.927G>Cp.Q309HSubstitution - Missense8:123504655-123504655-
RK167_C01COSM1635630c.677C>Ap.T226NSubstitution - Missense8:123506549-123506549-
ESCC_43COSM5629917c.402_403insATp.T135fs*4Insertion - Frameshift8:123514303-123514304-
PM-7COSM5619768c.449A>Gp.E150GSubstitution - Missense8:123514257-123514257-
TCGA-BR-4361-01COSM3896569c.937A>Gp.T313ASubstitution - Missense8:123504645-123504645-
TCGA-HU-A4GU-01COSM3896570c.421G>Ap.A141TSubstitution - Missense8:123514285-123514285-
MZ7-melCOSM22077c.1014G>Ap.E338ESubstitution - coding silent8:123503427-123503427-
TCGA-B5-A0JR-01COSM1095785c.417C>Tp.G139GSubstitution - coding silent8:123514289-123514289-
B54COSM1755554c.84G>Cp.E28DSubstitution - Missense8:123540931-123540931-
TCGA-CA-6717-01COSM1454668c.707T>Cp.I236TSubstitution - Missense8:123506519-123506519-
TCGA-AX-A0J0-01COSM1095789c.120C>Ap.Y40*Substitution - Nonsense8:123534811-123534811-
TCGA-EB-A5UL-06COSM3644836c.673T>Cp.F225LSubstitution - Missense8:123506553-123506553-
TCGA-WL-A834-01COSM4830503c.894C>Gp.F298LSubstitution - Missense8:123504688-123504688-
TCGA-BR-6852-01COSM3315903c.335C>Tp.A112VSubstitution - Missense8:123531935-123531935-
TCGA-CC-A7IJ-01COSM4924554c.61G>Ap.G21SSubstitution - Missense8:123540954-123540954-
585205COSM320380c.781G>Tp.E261*Substitution - Nonsense8:123506445-123506445-
TCGA-EW-A1J5-01COSM1488981c.340C>Gp.L114VSubstitution - Missense8:123531930-123531930-
12TCOSM109954c.408C>Tp.S136SSubstitution - coding silent8:123514298-123514298-
107529COSM94287c.327C>Gp.F109LSubstitution - Missense8:123531943-123531943-
587228COSM1206827c.392A>Gp.K131RSubstitution - Missense8:123514314-123514314-
1517_PTCOSM5757127c.592T>Cp.Y198HSubstitution - Missense8:123513257-123513257-
TCGA-HU-A4GT-01COSM3896570c.421G>Ap.A141TSubstitution - Missense8:123514285-123514285-
105538COSM94288c.212G>Cp.S71TSubstitution - Missense8:123534719-123534719-
B85-0-TumorCOSM1755553c.324C>Tp.D108DSubstitution - coding silent8:123531946-123531946-
TCGA-06-0130-01COSM3412739c.702G>Ap.L234LSubstitution - coding silent8:123506524-123506524-
2497774COSM5750601c.571G>Ap.G191RSubstitution - Missense8:123513278-123513278-
TCGA-FW-A3R5-06COSM3924589c.108C>Tp.D36DSubstitution - coding silent8:123540907-123540907-
TCGA-AP-A0LM-01COSM1095787c.280C>Tp.R94CSubstitution - Missense8:123531990-123531990-
TCGA-AA-A010-01COSM281095c.610C>Ap.L204ISubstitution - Missense8:123513239-123513239-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.403924;Hs.4039338q24.13606604
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
CAMissensep.Q76Hc.228G>T8124546943LUSC
CANonsensep.E261*c.781G>T8124518685SCLC
CG3-UTRSNV.c.1065+479G>C8124515137HC
CGMissensep.Q214Hc.642G>C8124525447BRCA
CTIntronicSNV.c.373-4243G>A8124530816CLL
CTMissensep.A141Tc.421G>A8124526525HNSC
CTMissensep.G222Sc.664G>A8124518802CM
CTMissensep.G243Ec.728G>A8124518738CM
CTSynonymousp.L234Lc.702G>A8124518764GBM
GAIntronicSNV.c.466+62C>T8124526418CM
GAMissensep.A112Vc.335C>T8124544175STAD
GAMissensep.L4Fc.10C>T8124553245CM
GASynonymousp.F33Fc.99C>T8124553156LUSC
GASynonymousp.G139Gc.417C>T8124526529UCEC
GASynonymousp.L37Lc.111C>T8124553144LUSC
GASynonymousp.L4Lc.12C>T8124553243CM
GASynonymousp.V301Vc.903C>T8124516919CM
GT3-UTRSNV.c.1065+3725C>A8124511891HC
TC3-UTRSNV.c.1065+3256A>G8124512360MB
TCMissensep.I140Vc.418A>G8124526528UCEC
TCMissensep.Y57Cc.170A>G8124547001LUSC
TCSynonymousp.A130Ac.390A>G8124526556BRCA