UBE2Q2
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA157616588976165889+Missense_MutationSNPCCGTCGA-DK-AA6S-01A-21D-A391-08TCGA-DK-AA6S-10A-01D-A394-08g.chr15:76165889C>Gc.568C>Gc.(568-570)Caa>Gaap.Q190E
BLCA157617150076171500+Missense_MutationSNPGGATCGA-XF-A9T0-01A-11D-A391-08TCGA-XF-A9T0-10A-01D-A394-08g.chr15:76171500G>Ac.796G>Ac.(796-798)Gaa>Aaap.E266K
BLCA157617576276175762+Missense_MutationSNPGGATCGA-XF-A9T0-01A-11D-A391-08TCGA-XF-A9T0-10A-01D-A394-08g.chr15:76175762G>Ac.881G>Ac.(880-882)gGa>gAap.G294E
BRCA157614674976146749+Missense_MutationSNPCCTTCGA-A8-A09B-01A-11W-A019-09TCGA-A8-A09B-10A-01W-A021-09g.chr15:76146749C>Tc.203C>Tc.(202-204)cCg>cTgp.P68L
BRCA157615222576152225+Missense_MutationSNPCCGTCGA-AC-A23H-01A-11D-A159-09TCGA-AC-A23H-11A-12D-A17G-09g.chr15:76152225C>Gc.289C>Gc.(289-291)Cag>Gagp.Q97E
CESC157613605576136055+Missense_MutationSNPCCGTCGA-IR-A3LA-01A-11D-A22X-09TCGA-IR-A3LA-10A-01D-A22X-09g.chr15:76136055C>Gc.48C>Gc.(46-48)atC>atGp.I16M
CHOL157618329876183298+Missense_MutationSNPGGATCGA-3X-AAVE-01A-11D-A417-09TCGA-3X-AAVE-10A-01D-A41A-09g.chr15:76183298G>Ac.972G>Ac.(970-972)atG>atAp.M324I
COAD157615222376152223+Missense_MutationSNPGGATCGA-AA-3713-01A-21D-1719-10TCGA-AA-3713-11A-01D-1719-10g.chr15:76152223G>Ac.287G>Ac.(286-288)cGt>cAtp.R96H
COAD157615222376152223+Missense_MutationSNPGGATCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr15:76152223G>Ac.287G>Ac.(286-288)cGt>cAtp.R96H
COAD157616134876161348+SilentSNPTTCTCGA-AA-3715-01A-01W-0900-09TCGA-AA-3715-10A-01W-0900-09g.chr15:76161348T>Cc.444T>Cc.(442-444)gcT>gcCp.A148A
COADREAD157615222376152223+Missense_MutationSNPGGATCGA-AA-3713-01A-21D-1719-10TCGA-AA-3713-11A-01D-1719-10g.chr15:76152223G>Ac.287G>Ac.(286-288)cGt>cAtp.R96H
COADREAD157615222376152223+Missense_MutationSNPGGATCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr15:76152223G>Ac.287G>Ac.(286-288)cGt>cAtp.R96H
COADREAD157616134876161348+SilentSNPTTCTCGA-AA-3715-01A-01W-0900-09TCGA-AA-3715-10A-01W-0900-09g.chr15:76161348T>Cc.444T>Cc.(442-444)gcT>gcCp.A148A
DLBC157616132876161330+In_Frame_DelDELGAAGAA-TCGA-GS-A9U3-01A-11D-A38X-10TCGA-GS-A9U3-10A-01D-A38X-10g.chr15:76161328_76161330delGAAc.424_426delGAAc.(424-426)gaadelp.E146del
GBMLGG157616589376165893+Missense_MutationSNPGGTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr15:76165893G>Tc.572G>Tc.(571-573)aGg>aTgp.R191M
HNSC157617151476171514+SilentSNPTTGTCGA-CR-7402-01A-11D-2012-08TCGA-CR-7402-10A-01D-2013-08g.chr15:76171514T>Gc.810T>Gc.(808-810)ctT>ctGp.L270L
HNSC157618329576183295+SilentSNPCCTTCGA-F7-A50J-01A-21D-A28R-08TCGA-F7-A50J-10A-01D-A28U-08g.chr15:76183295C>Tc.969C>Tc.(967-969)atC>atTp.I323I
LGG157616589376165893+Missense_MutationSNPGGTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr15:76165893G>Tc.572G>Tc.(571-573)aGg>aTgp.R191M
LIHC157615222976152229+Missense_MutationSNPAATTCGA-UB-A7MB-01A-11D-A33Q-10TCGA-UB-A7MB-10A-01D-A33Q-10g.chr15:76152229A>Tc.293A>Tc.(292-294)cAa>cTap.Q98L
LIHC157616579176165791+Missense_MutationSNPAAGTCGA-CC-A3M9-01A-11D-A20W-10TCGA-CC-A3M9-10A-01D-A20W-10g.chr15:76165791A>Gc.470A>Gc.(469-471)tAt>tGtp.Y157C
LIHC157618328976183289+SilentSNPGGCTCGA-DD-AACZ-01A-11D-A40R-10TCGA-DD-AACZ-10A-01D-A40U-10g.chr15:76183289G>Cc.963G>Cc.(961-963)tcG>tcCp.S321S
LIHC157618335276183352+SilentSNPTTCTCGA-UB-A7MB-01A-11D-A33Q-10TCGA-UB-A7MB-10A-01D-A33Q-10g.chr15:76183352T>Cc.1026T>Cc.(1024-1026)aaT>aaCp.N342N
LIHC157619176776191767+Splice_SiteSNPGGATCGA-2Y-A9GZ-01A-11D-A38X-10TCGA-2Y-A9GZ-10A-01D-A38X-10g.chr15:76191767G>Ac.e13-1
LUAD157615229176152291+Missense_MutationSNPGGCTCGA-95-7043-01A-11D-1945-08TCGA-95-7043-10A-01D-1946-08g.chr15:76152291G>Cc.355G>Cc.(355-357)Gag>Cagp.E119Q
LUAD157616130376161305+In_Frame_DelDELAGAAGA-TCGA-86-A4JF-01A-11D-A24P-08TCGA-86-A4JF-10A-01D-A24P-08g.chr15:76161303_76161305delAGAc.399_401delAGAc.(397-402)acagaa>acap.E135del
LUAD157616579876165798+Missense_MutationSNPGGATCGA-55-6982-01A-11D-1945-08TCGA-55-6982-11A-01D-1945-08g.chr15:76165798G>Ac.477G>Ac.(475-477)atG>atAp.M159I
LUAD157616852976168529+Splice_SiteSNPGGTTCGA-99-8028-01A-11D-2238-08TCGA-99-8028-10A-01D-2238-08g.chr15:76168529G>Tc.590G>Tc.(589-591)gGt>gTtp.G197V
LUAD157616854976168549+Nonsense_MutationSNPCCTTCGA-50-5933-01A-11D-1753-08TCGA-50-5933-11A-01D-1753-08g.chr15:76168549C>Tc.610C>Tc.(610-612)Caa>Taap.Q204*
LUAD157616861376168613+Splice_SiteSNPGGATCGA-91-6829-01A-21D-1855-08TCGA-91-6829-11A-01D-1855-08g.chr15:76168613G>Ac.e6+1
LUSC157615225576152255+Missense_MutationSNPTTCTCGA-18-3408-01A-01D-0983-08TCGA-18-3408-11A-01D-0983-08g.chr15:76152255T>Cc.319T>Cc.(319-321)Tgc>Cgcp.C107R
OV157616576876165768+Splice_SiteSNPGGTTCGA-13-1501-01A-01W-0545-08TCGA-13-1501-10A-01W-0546-08g.chr15:76165768G>Tc.e5-1
OV157617572776175727+SilentSNPTTCTCGA-29-2431-01A-01D-1526-09TCGA-29-2431-10A-01D-1526-09g.chr15:76175727T>Cc.846T>Cc.(844-846)ccT>ccCp.P282P
OV157619178376191783+Missense_MutationSNPCCGTCGA-25-1313-01A-01W-0492-08TCGA-25-1313-10A-01W-0492-08g.chr15:76191783C>Gc.1112C>Gc.(1111-1113)cCa>cGap.P371R
SKCM157614673176146731+Missense_MutationSNPCCTTCGA-FW-A3TV-06A-11D-A23B-08TCGA-FW-A3TV-10A-01D-A23B-08g.chr15:76146731C>Tc.185C>Tc.(184-186)tCc>tTcp.S62F
SKCM157617571676175716+Missense_MutationSNPCCTTCGA-EE-A3AC-06A-11D-A196-08TCGA-EE-A3AC-10A-01D-A198-08g.chr15:76175716C>Tc.835C>Tc.(835-837)Cca>Tcap.P279S
SKCM157617573776175737+Nonsense_MutationSNPCCTTCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr15:76175737C>Tc.856C>Tc.(856-858)Cga>Tgap.R286*
SKCM157619177976191779+Missense_MutationSNPCCTTCGA-D3-A51R-06A-11D-A25O-08TCGA-D3-A51R-10A-01D-A25O-08g.chr15:76191779C>Tc.1108C>Tc.(1108-1110)Cct>Tctp.P370S
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-US157619632976196329single base substitutionGAdownstream_gene_variant
BOCA-FR157613696476136964single base substitutionACintron_variant
BRCA-EU157613173976131739single base substitutionTAupstream_gene_variant
BRCA-EU157613187976131879single base substitutionTCupstream_gene_variant
BRCA-EU157613197976131979single base substitutionGCupstream_gene_variant
BRCA-EU157613326276133262single base substitutionCAupstream_gene_variant
BRCA-EU157613564676135646single base substitutionTC5_prime_UTR_variant
BRCA-EU157613564676135646single base substitutionTCupstream_gene_variant
BRCA-EU157613650976136509single base substitutionCT5_prime_UTR_variant
BRCA-EU157613650976136509single base substitutionCTexon_variant
BRCA-EU157613650976136509single base substitutionCTintron_variant
BRCA-EU157613861876138618single base substitutionGAintron_variant
BRCA-EU157613997176139971single base substitutionCAintron_variant
BRCA-EU157614029576140295single base substitutionCTintron_variant
BRCA-EU157614126176141261single base substitutionGTintron_variant
BRCA-EU157614293076142930single base substitutionGAintron_variant
BRCA-EU157614438876144388single base substitutionTAintron_variant
BRCA-EU157614782476147824single base substitutionTGintron_variant
BRCA-EU157614782476147824single base substitutionTGupstream_gene_variant
BRCA-EU157615060376150603single base substitutionTCintron_variant
BRCA-EU157615060376150603single base substitutionTCupstream_gene_variant
BRCA-EU157615146676151466single base substitutionTCintron_variant
BRCA-EU157615146676151466single base substitutionTCupstream_gene_variant
BRCA-EU157615162176151621single base substitutionGAintron_variant
BRCA-EU157615162176151621single base substitutionGAupstream_gene_variant
BRCA-EU157615789276157892single base substitutionCTintron_variant
BRCA-EU157615789276157892single base substitutionCTupstream_gene_variant
BRCA-EU157615815976158159single base substitutionTAintron_variant
BRCA-EU157615815976158159single base substitutionTAupstream_gene_variant
BRCA-EU157615833176158331single base substitutionGCintron_variant
BRCA-EU157615833176158331single base substitutionGCupstream_gene_variant
BRCA-EU157615838076158380single base substitutionCAintron_variant
BRCA-EU157615838076158380single base substitutionCAupstream_gene_variant
BRCA-EU157615892876158928single base substitutionTGintron_variant
BRCA-EU157615892876158928single base substitutionTGupstream_gene_variant
BRCA-EU157615962576159625single base substitutionAGintron_variant
BRCA-EU157615962576159625single base substitutionAGupstream_gene_variant
BRCA-EU157616038076160380single base substitutionTCintron_variant
BRCA-EU157616038076160380single base substitutionTCupstream_gene_variant
BRCA-EU157616635576166355single base substitutionCTintron_variant
BRCA-EU157616635576166355single base substitutionCTupstream_gene_variant
BRCA-EU157616746576167465single base substitutionCGintron_variant
BRCA-EU157616746576167465single base substitutionCGupstream_gene_variant
BRCA-EU157616792076167920single base substitutionCAintron_variant
BRCA-EU157616792076167920single base substitutionCAupstream_gene_variant
BRCA-EU157616793476167934single base substitutionGAintron_variant
BRCA-EU157616793476167934single base substitutionGAupstream_gene_variant
BRCA-EU157617014276170142single base substitutionCAintron_variant
BRCA-EU157617014276170142single base substitutionCAupstream_gene_variant
BRCA-EU157617167976171679single base substitutionCTintron_variant
BRCA-EU157617170976171709single base substitutionCTintron_variant
BRCA-EU157617298776172996deletion of <=200bpATGTGCCACT-intron_variant
BRCA-EU157617313376173133single base substitutionGTintron_variant
BRCA-EU157617682076176820single base substitutionCGintron_variant
BRCA-EU157617773576177735single base substitutionGTintron_variant
BRCA-EU157617855976178559single base substitutionCGintron_variant
BRCA-EU157617986576179865single base substitutionTCintron_variant
BRCA-EU157618004176180041single base substitutionATintron_variant
BRCA-EU157618056576180565single base substitutionGAintron_variant
BRCA-EU157618322176183221single base substitutionAGintron_variant
BRCA-EU157618526376185263single base substitutionGTintron_variant
BRCA-EU157618718976187189single base substitutionTCintron_variant
BRCA-EU157618774976187749single base substitutionCGintron_variant
BRCA-EU157618900476189004single base substitutionATintron_variant
BRCA-EU157619105276191052single base substitutionCTdownstream_gene_variant
BRCA-EU157619105276191052single base substitutionCTintron_variant
BRCA-EU157619156076191560single base substitutionGAdownstream_gene_variant
BRCA-EU157619156076191560single base substitutionGAintron_variant
BRCA-EU157619164476191644deletion of <=200bpA-downstream_gene_variant
BRCA-EU157619164476191644deletion of <=200bpA-intron_variant
BRCA-EU157619194976191949single base substitutionGC3_prime_UTR_variant
BRCA-EU157619194976191949single base substitutionGCdownstream_gene_variant
BRCA-EU157619412976194129single base substitutionCGdownstream_gene_variant
BRCA-EU157619487476194874deletion of <=200bpA-downstream_gene_variant
BRCA-EU157619501376195013single base substitutionTAdownstream_gene_variant
BRCA-EU157619613276196132single base substitutionCGdownstream_gene_variant
BRCA-EU157619682976196829single base substitutionCTdownstream_gene_variant
BRCA-EU157619728176197281single base substitutionCAdownstream_gene_variant
BRCA-EU157619740576197405single base substitutionCAdownstream_gene_variant
BRCA-EU157619781776197817single base substitutionCGdownstream_gene_variant
BRCA-FR157614782476147824single base substitutionTGintron_variant
BRCA-FR157614782476147824single base substitutionTGupstream_gene_variant
BRCA-FR157615803976158039single base substitutionACintron_variant
BRCA-FR157615803976158039single base substitutionACupstream_gene_variant
BRCA-FR157617657376176573single base substitutionCAintron_variant
BRCA-FR157619613276196132single base substitutionCGdownstream_gene_variant
BRCA-FR157619682976196829single base substitutionCTdownstream_gene_variant
BRCA-FR157619728176197281single base substitutionCAdownstream_gene_variant
BRCA-FR157619781776197817single base substitutionCGdownstream_gene_variant
BRCA-UK157614126176141261single base substitutionGTintron_variant
BRCA-UK157619826076198260single base substitutionCAdownstream_gene_variant
BRCA-US157613650976136509single base substitutionCT5_prime_UTR_variant
BRCA-US157613650976136509single base substitutionCTexon_variant
BRCA-US157613650976136509single base substitutionCTintron_variant
BRCA-US157613668576136685single base substitutionGT5_prime_UTR_variant
BRCA-US157613668576136685single base substitutionGTexon_variant
BRCA-US157613668576136685single base substitutionGTintron_variant
BRCA-US157614674976146749single base substitutionCTexon_variant
BRCA-US157614674976146749single base substitutionCTmissense_variantP52L155C>T
BRCA-US157614674976146749single base substitutionCTmissense_variantP68L203C>T
BRCA-US157615222576152225single base substitutionCGexon_variant
BRCA-US157615222576152225single base substitutionCGintron_variant
BRCA-US157615222576152225single base substitutionCGmissense_variantQ81E241C>G
BRCA-US157615222576152225single base substitutionCGmissense_variantQ97E289C>G
BRCA-US157615222576152225single base substitutionCGupstream_gene_variant
BRCA-US157619684576196845single base substitutionTCdownstream_gene_variant
BTCA-JP157616150876161508single base substitutionCGintron_variant
BTCA-JP157617164876171648single base substitutionCTintron_variant
BTCA-JP157618953976189539single base substitutionTCdownstream_gene_variant
BTCA-JP157618953976189539single base substitutionTCintron_variant
CESC-US157613605576136055single base substitutionCGexon_variant
CESC-US157613605576136055single base substitutionCGmissense_variantI16M48C>G
CESC-US157613605576136055single base substitutionCGupstream_gene_variant
CESC-US157613666076136660single base substitutionTC5_prime_UTR_premature_start_codon_gain_variant
CESC-US157613666076136660single base substitutionTCexon_variant
CESC-US157613666076136660single base substitutionTCintron_variant
CLLE-ES157613806376138063single base substitutionACintron_variant
CLLE-ES157615120176151202deletion of <=200bpTT-intron_variant
CLLE-ES157615120176151202deletion of <=200bpTT-upstream_gene_variant
CLLE-ES157617910776179107single base substitutionATintron_variant
CLLE-ES157619660076196600single base substitutionCTdownstream_gene_variant
COAD-US157613676876136768single base substitutionCTexon_variant
COAD-US157613676876136768single base substitutionCTintron_variant
COAD-US157613676876136768single base substitutionCTmissense_variantP25L74C>T
COAD-US157615222376152223single base substitutionGAexon_variant
COAD-US157615222376152223single base substitutionGAintron_variant
COAD-US157615222376152223single base substitutionGAmissense_variantR80H239G>A
COAD-US157615222376152223single base substitutionGAmissense_variantR96H287G>A
COAD-US157615222376152223single base substitutionGAupstream_gene_variant
COAD-US157619640876196408single base substitutionCTdownstream_gene_variant
COCA-CN157616131276161312single base substitutionGTexon_variant
COCA-CN157616131276161312single base substitutionGTintron_variant
COCA-CN157616131276161312single base substitutionGTsynonymous_variantV101V303G>T
COCA-CN157616131276161312single base substitutionGTsynonymous_variantV120V360G>T
COCA-CN157616131276161312single base substitutionGTsynonymous_variantV136V408G>T
COCA-CN157616131276161312single base substitutionGTsynonymous_variantV21V63G>T
COCA-CN157616134876161348single base substitutionTGexon_variant
COCA-CN157616134876161348single base substitutionTGintron_variant
COCA-CN157616134876161348single base substitutionTGsynonymous_variantA113A339T>G
COCA-CN157616134876161348single base substitutionTGsynonymous_variantA132A396T>G
COCA-CN157616134876161348single base substitutionTGsynonymous_variantA148A444T>G
COCA-CN157616134876161348single base substitutionTGsynonymous_variantA33A99T>G
COCA-CN157619191076191910single base substitutionAC3_prime_UTR_variant
COCA-CN157619191076191910single base substitutionACdownstream_gene_variant
EOPC-DE157617852576178525single base substitutionAGintron_variant
ESAD-UK157613088776130887single base substitutionACupstream_gene_variant
ESAD-UK157613223976132239single base substitutionACupstream_gene_variant
ESAD-UK157613348276133482single base substitutionAGupstream_gene_variant
ESAD-UK157613414676134146single base substitutionGTupstream_gene_variant
ESAD-UK157613448276134482single base substitutionCTupstream_gene_variant
ESAD-UK157613562576135625single base substitutionCG5_prime_UTR_variant
ESAD-UK157613562576135625single base substitutionCGupstream_gene_variant
ESAD-UK157613644976136449single base substitutionCA5_prime_UTR_variant
ESAD-UK157613644976136449single base substitutionCAintron_variant
ESAD-UK157613644976136449single base substitutionCAupstream_gene_variant
ESAD-UK157613730876137308single base substitutionCAintron_variant
ESAD-UK157613807576138075single base substitutionCTintron_variant
ESAD-UK157614366176143661single base substitutionCGintron_variant
ESAD-UK157614395776143957single base substitutionTAintron_variant
ESAD-UK157614395976143959single base substitutionGAintron_variant
ESAD-UK157614583276145833deletion of <=200bpTA-intron_variant
ESAD-UK157615043076150430single base substitutionCTintron_variant
ESAD-UK157615043076150430single base substitutionCTupstream_gene_variant
ESAD-UK157615255276152552single base substitutionCAdownstream_gene_variant
ESAD-UK157615255276152552single base substitutionCAintron_variant
ESAD-UK157615340876153408single base substitutionCTdownstream_gene_variant
ESAD-UK157615340876153408single base substitutionCTintron_variant
ESAD-UK157615366376153663single base substitutionGAdownstream_gene_variant
ESAD-UK157615366376153663single base substitutionGAintron_variant
ESAD-UK157615800776158007single base substitutionTCintron_variant
ESAD-UK157615800776158007single base substitutionTCupstream_gene_variant
ESAD-UK157615981676159816single base substitutionTCintron_variant
ESAD-UK157615981676159816single base substitutionTCupstream_gene_variant
ESAD-UK157616017576160175single base substitutionCGintron_variant
ESAD-UK157616017576160175single base substitutionCGupstream_gene_variant
ESAD-UK157616301176163011single base substitutionCTintron_variant
ESAD-UK157616376076163760single base substitutionGAintron_variant
ESAD-UK157617020576170205single base substitutionTGintron_variant
ESAD-UK157617020576170205single base substitutionTGupstream_gene_variant
ESAD-UK157617153176171531single base substitutionTAintron_variant
ESAD-UK157617153176171531single base substitutionTAsplice_donor_variant
ESAD-UK157617165476171654single base substitutionCAintron_variant
ESAD-UK157617577876175778single base substitutionGTintron_variant
ESAD-UK157617746276177462single base substitutionTGintron_variant
ESAD-UK157617752276177522single base substitutionGAintron_variant
ESAD-UK157617754376177543single base substitutionCTintron_variant
ESAD-UK157617921176179211insertion of <=200bp-Gintron_variant
ESAD-UK157617996176179961single base substitutionCTintron_variant
ESAD-UK157618078576180785single base substitutionCTintron_variant
ESAD-UK157618100176181001single base substitutionGAintron_variant
ESAD-UK157618248276182482single base substitutionTAintron_variant
ESAD-UK157618510876185108single base substitutionTGintron_variant
ESAD-UK157618590476185904single base substitutionCAintron_variant
ESAD-UK157618600776186007single base substitutionACintron_variant
ESAD-UK157618661076186610deletion of <=200bpA-intron_variant
ESAD-UK157618786376187863single base substitutionAGintron_variant
ESAD-UK157618810676188106single base substitutionAGintron_variant
ESAD-UK157618966576189665single base substitutionCAdownstream_gene_variant
ESAD-UK157618966576189665single base substitutionCAintron_variant
ESCA-CN157614667376146673single base substitutionAGintron_variant
ESCA-CN157619163276191633deletion of <=200bpAT-downstream_gene_variant
ESCA-CN157619163276191633deletion of <=200bpAT-intron_variant
GBM-US157619683876196838single base substitutionCTdownstream_gene_variant
LICA-CN157619683576196835single base substitutionGTdownstream_gene_variant
LICA-FR157615297076152970single base substitutionAGdownstream_gene_variant
LICA-FR157615297076152970single base substitutionAGintron_variant
LICA-FR157615786276157862single base substitutionTCintron_variant
LICA-FR157615786276157862single base substitutionTCupstream_gene_variant
LICA-FR157617113076171130single base substitutionTGintron_variant
LIHC-US157615222976152229single base substitutionATdownstream_gene_variant
LIHC-US157615222976152229single base substitutionATintron_variant
LIHC-US157615222976152229single base substitutionATmissense_variantQ82L245A>T
LIHC-US157615222976152229single base substitutionATmissense_variantQ98L293A>T
LIHC-US157615222976152229single base substitutionATupstream_gene_variant
LIHC-US157616579176165791single base substitutionAGexon_variant
LIHC-US157616579176165791single base substitutionAGintron_variant
LIHC-US157616579176165791single base substitutionAGmissense_variantY122C365A>G
LIHC-US157616579176165791single base substitutionAGmissense_variantY141C422A>G
LIHC-US157616579176165791single base substitutionAGmissense_variantY157C470A>G
LIHC-US157616579176165791single base substitutionAGmissense_variantY42C125A>G
LIHC-US157616579176165791single base substitutionAGupstream_gene_variant
LIHC-US157618335276183352single base substitutionTCexon_variant
LIHC-US157618335276183352single base substitutionTCintron_variant
LIHC-US157618335276183352single base substitutionTCsynonymous_variantN307N921T>C
LIHC-US157618335276183352single base substitutionTCsynonymous_variantN326N978T>C
LIHC-US157618335276183352single base substitutionTCsynonymous_variantN342N1026T>C
LINC-JP157615082076150820single base substitutionCTintron_variant
LINC-JP157615082076150820single base substitutionCTupstream_gene_variant
LINC-JP157615783876157838single base substitutionAGintron_variant
LINC-JP157615783876157838single base substitutionAGupstream_gene_variant
LINC-JP157616136776161367single base substitutionAGintron_variant
LINC-JP157616666976166669single base substitutionGTintron_variant
LINC-JP157616666976166669single base substitutionGTupstream_gene_variant
LINC-JP157616764276167642single base substitutionCTintron_variant
LINC-JP157616764276167642single base substitutionCTupstream_gene_variant
LINC-JP157616859576168595single base substitutionCTintron_variant
LINC-JP157616859576168595single base substitutionCTmissense_variantS104L311C>T
LINC-JP157616859576168595single base substitutionCTmissense_variantS184L551C>T
LINC-JP157616859576168595single base substitutionCTmissense_variantS203L608C>T
LINC-JP157616859576168595single base substitutionCTmissense_variantS219L656C>T
LINC-JP157616859576168595single base substitutionCTupstream_gene_variant
LINC-JP157618280676182806single base substitutionGTexon_variant
LINC-JP157618280676182806single base substitutionGTintron_variant
LINC-JP157618280676182806single base substitutionGTmissense_variantM270I810G>T
LINC-JP157618280676182806single base substitutionGTmissense_variantM289I867G>T
LINC-JP157618280676182806single base substitutionGTmissense_variantM305I915G>T
LINC-JP157618333476183334single base substitutionACexon_variant
LINC-JP157618333476183334single base substitutionACintron_variant
LINC-JP157618333476183334single base substitutionACmissense_variantR301S903A>C
LINC-JP157618333476183334single base substitutionACmissense_variantR320S960A>C
LINC-JP157618333476183334single base substitutionACmissense_variantR336S1008A>C
LINC-JP157618930376189303single base substitutionAGintron_variant
LINC-JP157618994076189940deletion of <=200bpT-downstream_gene_variant
LINC-JP157618994076189940deletion of <=200bpT-intron_variant
LINC-JP157619625876196258single base substitutionGAdownstream_gene_variant
LIRI-JP157613203976132039single base substitutionTCupstream_gene_variant
LIRI-JP157613217676132176single base substitutionGAupstream_gene_variant
LIRI-JP157613248976132489single base substitutionGAupstream_gene_variant
LIRI-JP157613376576133765single base substitutionTGupstream_gene_variant
LIRI-JP157613448976134489single base substitutionCGupstream_gene_variant
LIRI-JP157613462576134625single base substitutionACupstream_gene_variant
LIRI-JP157614031776140317single base substitutionGAintron_variant
LIRI-JP157614033576140335single base substitutionGAintron_variant
LIRI-JP157614069976140699single base substitutionAGintron_variant
LIRI-JP157614087776140877single base substitutionTCintron_variant
LIRI-JP157614194176141941single base substitutionCTintron_variant
LIRI-JP157614505476145054single base substitutionATintron_variant
LIRI-JP157614674076146740single base substitutionCTexon_variant
LIRI-JP157614674076146740single base substitutionCTmissense_variantS49F146C>T
LIRI-JP157614674076146740single base substitutionCTmissense_variantS65F194C>T
LIRI-JP157614821476148214single base substitutionGAintron_variant
LIRI-JP157614821476148214single base substitutionGAupstream_gene_variant
LIRI-JP157614915876149158single base substitutionAGintron_variant
LIRI-JP157614915876149158single base substitutionAGupstream_gene_variant
LIRI-JP157614962776149627single base substitutionAGintron_variant
LIRI-JP157614962776149627single base substitutionAGupstream_gene_variant
LIRI-JP157616022376160223single base substitutionAGintron_variant
LIRI-JP157616022376160223single base substitutionAGupstream_gene_variant
LIRI-JP157616127176161271single base substitutionCAintron_variant
LIRI-JP157616127176161271single base substitutionCAupstream_gene_variant
LIRI-JP157616157676161576single base substitutionGTintron_variant
LIRI-JP157617011776170117single base substitutionAGintron_variant
LIRI-JP157617011776170117single base substitutionAGupstream_gene_variant
LIRI-JP157617040576170405single base substitutionAGintron_variant
LIRI-JP157617040576170405single base substitutionAGupstream_gene_variant
LIRI-JP157617140076171400single base substitutionAGintron_variant
LIRI-JP157617222476172224single base substitutionATintron_variant
LIRI-JP157617364476173644single base substitutionTCintron_variant
LIRI-JP157617484476174844single base substitutionGAintron_variant
LIRI-JP157617988976179889single base substitutionTAintron_variant
LIRI-JP157618010576180105single base substitutionTCintron_variant
LIRI-JP157618016976180169single base substitutionGTintron_variant
LIRI-JP157618141376181413single base substitutionCAintron_variant
LIRI-JP157618327676183276single base substitutionAGexon_variant
LIRI-JP157618327676183276single base substitutionAGintron_variant
LIRI-JP157618327676183276single base substitutionAGmissense_variantY282C845A>G
LIRI-JP157618327676183276single base substitutionAGmissense_variantY301C902A>G
LIRI-JP157618327676183276single base substitutionAGmissense_variantY317C950A>G
LIRI-JP157618441576184415single base substitutionATintron_variant
LIRI-JP157618475076184750single base substitutionAGintron_variant
LIRI-JP157618523476185234single base substitutionTCintron_variant
LIRI-JP157618578176185781single base substitutionTCintron_variant
LIRI-JP157618716576187165single base substitutionCTintron_variant
LIRI-JP157618727976187279single base substitutionGAintron_variant
LIRI-JP157618812276188122single base substitutionGCintron_variant
LIRI-JP157619193876191938single base substitutionTC3_prime_UTR_variant
LIRI-JP157619193876191938single base substitutionTCdownstream_gene_variant
LIRI-JP157619215076192150single base substitutionAG3_prime_UTR_variant
LIRI-JP157619215076192150single base substitutionAGdownstream_gene_variant
LIRI-JP157619429476194294single base substitutionGAdownstream_gene_variant
LUSC-KR157613139976131399single base substitutionGAupstream_gene_variant
LUSC-KR157615167476151674single base substitutionGCintron_variant
LUSC-KR157615167476151674single base substitutionGCupstream_gene_variant
LUSC-KR157615584576155845single base substitutionCAdownstream_gene_variant
LUSC-KR157615584576155845single base substitutionCAintron_variant
LUSC-KR157615816376158163single base substitutionCTintron_variant
LUSC-KR157615816376158163single base substitutionCTupstream_gene_variant
LUSC-KR157616332076163320single base substitutionGAintron_variant
LUSC-KR157617090176170901single base substitutionAGintron_variant
LUSC-KR157617689376176893single base substitutionGAintron_variant
LUSC-KR157617746276177462single base substitutionTGintron_variant
LUSC-KR157618100076181000single base substitutionCGintron_variant
LUSC-KR157619325476193254single base substitutionAT3_prime_UTR_variant
LUSC-KR157619325476193254single base substitutionATdownstream_gene_variant
LUSC-KR157619670976196709single base substitutionCTdownstream_gene_variant
LUSC-US157615225576152255single base substitutionTCdownstream_gene_variant
LUSC-US157615225576152255single base substitutionTCintron_variant
LUSC-US157615225576152255single base substitutionTCmissense_variantC107R319T>C
LUSC-US157615225576152255single base substitutionTCmissense_variantC91R271T>C
LUSC-US157615225576152255single base substitutionTCupstream_gene_variant
MALY-DE157613283076132830single base substitutionGTupstream_gene_variant
MALY-DE157613385576133855single base substitutionAGupstream_gene_variant
MALY-DE157613747576137475single base substitutionCTintron_variant
MALY-DE157615577676155776single base substitutionTGdownstream_gene_variant
MALY-DE157615577676155776single base substitutionTGintron_variant
MALY-DE157615717176157171single base substitutionCGdownstream_gene_variant
MALY-DE157615717176157171single base substitutionCGintron_variant
MALY-DE157615717176157171single base substitutionCGupstream_gene_variant
MALY-DE157616058276160582single base substitutionTGintron_variant
MALY-DE157616058276160582single base substitutionTGupstream_gene_variant
MALY-DE157616677376166773single base substitutionCTintron_variant
MALY-DE157616677376166773single base substitutionCTupstream_gene_variant
MALY-DE157616897976168979single base substitutionATintron_variant
MALY-DE157616897976168979single base substitutionATupstream_gene_variant
MALY-DE157617283076172830single base substitutionTCintron_variant
MALY-DE157617653376176533single base substitutionAGintron_variant
MALY-DE157618205176182051single base substitutionAGintron_variant
MALY-DE157618779776187797single base substitutionTAintron_variant
MALY-DE157618830976188309single base substitutionAGintron_variant
MALY-DE157619479276194792single base substitutionCTdownstream_gene_variant
MALY-DE157619642676196426single base substitutionCTdownstream_gene_variant
MELA-AU157613096976130969single base substitutionGAupstream_gene_variant
MELA-AU157613123176131231single base substitutionCTupstream_gene_variant
MELA-AU157613167776131677single base substitutionCTupstream_gene_variant
MELA-AU157613180476131804single base substitutionGAupstream_gene_variant
MELA-AU157613202476132024single base substitutionCTupstream_gene_variant
MELA-AU157613202976132029single base substitutionGAupstream_gene_variant
MELA-AU157613203276132032single base substitutionCTupstream_gene_variant
MELA-AU157613209576132095single base substitutionTCupstream_gene_variant
MELA-AU157613239776132397single base substitutionCTupstream_gene_variant
MELA-AU157613242076132420single base substitutionGAupstream_gene_variant
MELA-AU157613256876132568single base substitutionGAupstream_gene_variant
MELA-AU157613316376133163single base substitutionGAupstream_gene_variant
MELA-AU157613374176133741single base substitutionTAupstream_gene_variant
MELA-AU157613448376134483single base substitutionGAupstream_gene_variant
MELA-AU157613472276134722single base substitutionGAupstream_gene_variant
MELA-AU157613534276135342single base substitutionGAupstream_gene_variant
MELA-AU157613631776136317single base substitutionCTintron_variant
MELA-AU157613631776136317single base substitutionCTupstream_gene_variant
MELA-AU157613638976136389single base substitutionCA5_prime_UTR_variant
MELA-AU157613638976136389single base substitutionCAintron_variant
MELA-AU157613638976136389single base substitutionCAupstream_gene_variant
MELA-AU157613766676137666single base substitutionCTintron_variant
MELA-AU157613854376138543single base substitutionCTintron_variant
MELA-AU157613904276139042single base substitutionTCintron_variant
MELA-AU157614021576140215single base substitutionGTintron_variant
MELA-AU157614062776140627single base substitutionCTintron_variant
MELA-AU157614085276140852single base substitutionTGintron_variant
MELA-AU157614097076140970single base substitutionCTintron_variant
MELA-AU157614098876140988single base substitutionCTintron_variant
MELA-AU157614113876141139multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU157614133276141332single base substitutionGTintron_variant
MELA-AU157614160476141604single base substitutionATintron_variant
MELA-AU157614188176141881single base substitutionCTintron_variant
MELA-AU157614218376142183single base substitutionCTintron_variant
MELA-AU157614252476142524single base substitutionGAintron_variant
MELA-AU157614266876142669multiple base substitution (>=2bp and <=200bp)GTAAintron_variant
MELA-AU157614394576143945single base substitutionCTintron_variant
MELA-AU157614405376144053single base substitutionCTintron_variant
MELA-AU157614441776144417single base substitutionCTintron_variant
MELA-AU157614563176145631single base substitutionTCintron_variant
MELA-AU157614625476146254single base substitutionCTintron_variant
MELA-AU157614668776146687single base substitutionCTintron_variant
MELA-AU157614705476147054single base substitutionTCintron_variant
MELA-AU157614778676147786single base substitutionCTintron_variant
MELA-AU157614778676147786single base substitutionCTupstream_gene_variant
MELA-AU157614823076148230single base substitutionCTintron_variant
MELA-AU157614823076148230single base substitutionCTupstream_gene_variant
MELA-AU157614857376148573single base substitutionTCintron_variant
MELA-AU157614857376148573single base substitutionTCupstream_gene_variant
MELA-AU157614994276149942single base substitutionCTintron_variant
MELA-AU157614994276149942single base substitutionCTupstream_gene_variant
MELA-AU157615045676150456single base substitutionCTintron_variant
MELA-AU157615045676150456single base substitutionCTupstream_gene_variant
MELA-AU157615088076150880single base substitutionCTintron_variant
MELA-AU157615088076150880single base substitutionCTupstream_gene_variant
MELA-AU157615104676151047multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU157615104676151047multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU157615119676151196single base substitutionCTintron_variant
MELA-AU157615119676151196single base substitutionCTupstream_gene_variant
MELA-AU157615126976151269single base substitutionCTintron_variant
MELA-AU157615126976151269single base substitutionCTupstream_gene_variant
MELA-AU157615145276151452single base substitutionCTintron_variant
MELA-AU157615145276151452single base substitutionCTupstream_gene_variant
MELA-AU157615151476151514single base substitutionCTintron_variant
MELA-AU157615151476151514single base substitutionCTupstream_gene_variant
MELA-AU157615180376151803single base substitutionCTintron_variant
MELA-AU157615180376151803single base substitutionCTupstream_gene_variant
MELA-AU157615191076151910single base substitutionTCintron_variant
MELA-AU157615191076151910single base substitutionTCupstream_gene_variant
MELA-AU157615251176152511single base substitutionGAdownstream_gene_variant
MELA-AU157615251176152511single base substitutionGAintron_variant
MELA-AU157615307576153075single base substitutionCTdownstream_gene_variant
MELA-AU157615307576153075single base substitutionCTintron_variant
MELA-AU157615312476153124single base substitutionCTdownstream_gene_variant
MELA-AU157615312476153124single base substitutionCTintron_variant
MELA-AU157615323276153232single base substitutionCTdownstream_gene_variant
MELA-AU157615323276153232single base substitutionCTintron_variant
MELA-AU157615374276153742single base substitutionCTdownstream_gene_variant
MELA-AU157615374276153742single base substitutionCTintron_variant
MELA-AU157615389976153899single base substitutionAGdownstream_gene_variant
MELA-AU157615389976153899single base substitutionAGintron_variant
MELA-AU157615436476154364single base substitutionCTdownstream_gene_variant
MELA-AU157615436476154364single base substitutionCTintron_variant
MELA-AU157615465276154652single base substitutionCTdownstream_gene_variant
MELA-AU157615465276154652single base substitutionCTintron_variant
MELA-AU157615474476154744single base substitutionCTdownstream_gene_variant
MELA-AU157615474476154744single base substitutionCTintron_variant
MELA-AU157615482976154830multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU157615482976154830multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU157615483076154830single base substitutionCTdownstream_gene_variant
MELA-AU157615483076154830single base substitutionCTintron_variant
MELA-AU157615552076155520single base substitutionCAdownstream_gene_variant
MELA-AU157615552076155520single base substitutionCAintron_variant
MELA-AU157615557676155576single base substitutionCTdownstream_gene_variant
MELA-AU157615557676155576single base substitutionCTintron_variant
MELA-AU157615628176156282multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU157615628176156282multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU157615641576156415single base substitutionCTdownstream_gene_variant
MELA-AU157615641576156415single base substitutionCTintron_variant
MELA-AU157615641576156415single base substitutionCTupstream_gene_variant
MELA-AU157615650676156514deletion of <=200bpAGTAAGGTT-downstream_gene_variant
MELA-AU157615650676156514deletion of <=200bpAGTAAGGTT-intron_variant
MELA-AU157615650676156514deletion of <=200bpAGTAAGGTT-upstream_gene_variant
MELA-AU157615659576156595single base substitutionTCdownstream_gene_variant
MELA-AU157615659576156595single base substitutionTCintron_variant
MELA-AU157615659576156595single base substitutionTCupstream_gene_variant
MELA-AU157615688876156888single base substitutionCTdownstream_gene_variant
MELA-AU157615688876156888single base substitutionCTintron_variant
MELA-AU157615688876156888single base substitutionCTupstream_gene_variant
MELA-AU157615752076157520single base substitutionCTintron_variant
MELA-AU157615752076157520single base substitutionCTupstream_gene_variant
MELA-AU157615793976157939single base substitutionTAintron_variant
MELA-AU157615793976157939single base substitutionTAupstream_gene_variant
MELA-AU157615808676158086single base substitutionCTintron_variant
MELA-AU157615808676158086single base substitutionCTupstream_gene_variant
MELA-AU157615899976158999single base substitutionCTintron_variant
MELA-AU157615899976158999single base substitutionCTupstream_gene_variant
MELA-AU157615946876159468single base substitutionGAintron_variant
MELA-AU157615946876159468single base substitutionGAupstream_gene_variant
MELA-AU157616040976160409single base substitutionCTintron_variant
MELA-AU157616040976160409single base substitutionCTupstream_gene_variant
MELA-AU157616052376160523single base substitutionCTintron_variant
MELA-AU157616052376160523single base substitutionCTupstream_gene_variant
MELA-AU157616064576160646multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU157616064576160646multiple base substitution (>=2bp and <=200bp)CCTTupstream_gene_variant
MELA-AU157616070876160708single base substitutionTCintron_variant
MELA-AU157616070876160708single base substitutionTCupstream_gene_variant
MELA-AU157616200276162002single base substitutionCTintron_variant
MELA-AU157616200476162004single base substitutionCAintron_variant
MELA-AU157616275376162753single base substitutionAGintron_variant
MELA-AU157616287276162872single base substitutionTAintron_variant
MELA-AU157616292276162923multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU157616295276162952single base substitutionGAintron_variant
MELA-AU157616377376163773single base substitutionCTintron_variant
MELA-AU157616386376163864multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU157616544576165467deletion of <=200bpAAGGTTCTTGACACCTGCTGCTA-intron_variant
MELA-AU157616606876166068single base substitutionCTintron_variant
MELA-AU157616606876166068single base substitutionCTupstream_gene_variant
MELA-AU157616643776166437single base substitutionCTintron_variant
MELA-AU157616643776166437single base substitutionCTupstream_gene_variant
MELA-AU157616657976166579single base substitutionCTintron_variant
MELA-AU157616657976166579single base substitutionCTupstream_gene_variant
MELA-AU157616671676166716single base substitutionCTintron_variant
MELA-AU157616671676166716single base substitutionCTupstream_gene_variant
MELA-AU157616830276168302single base substitutionGAintron_variant
MELA-AU157616830276168302single base substitutionGAupstream_gene_variant
MELA-AU157616843976168439single base substitutionCTintron_variant
MELA-AU157616843976168439single base substitutionCTupstream_gene_variant
MELA-AU157616933076169330single base substitutionCTintron_variant
MELA-AU157616933076169330single base substitutionCTupstream_gene_variant
MELA-AU157616942676169426single base substitutionCTintron_variant
MELA-AU157616942676169426single base substitutionCTupstream_gene_variant
MELA-AU157616963476169634single base substitutionCTintron_variant
MELA-AU157616963476169634single base substitutionCTupstream_gene_variant
MELA-AU157616980476169804single base substitutionCTintron_variant
MELA-AU157616980476169804single base substitutionCTupstream_gene_variant
MELA-AU157617026976170270multiple base substitution (>=2bp and <=200bp)GAATintron_variant
MELA-AU157617026976170270multiple base substitution (>=2bp and <=200bp)GAATupstream_gene_variant
MELA-AU157617042976170429single base substitutionCTintron_variant
MELA-AU157617042976170429single base substitutionCTupstream_gene_variant
MELA-AU157617108376171083single base substitutionCTintron_variant
MELA-AU157617166076171660single base substitutionCTintron_variant
MELA-AU157617187976171879single base substitutionCTintron_variant
MELA-AU157617226176172261single base substitutionCTintron_variant
MELA-AU157617245376172453single base substitutionGTintron_variant
MELA-AU157617252276172523multiple base substitution (>=2bp and <=200bp)TGCTintron_variant
MELA-AU157617318976173189single base substitutionAGintron_variant
MELA-AU157617320376173203single base substitutionCTintron_variant
MELA-AU157617402976174029single base substitutionCTintron_variant
MELA-AU157617417176174171single base substitutionCTintron_variant
MELA-AU157617450476174504single base substitutionCGintron_variant
MELA-AU157617529176175291single base substitutionCTintron_variant
MELA-AU157617539776175397single base substitutionCTintron_variant
MELA-AU157617544776175447single base substitutionCTintron_variant
MELA-AU157617576176175761single base substitutionGAexon_variant
MELA-AU157617576176175761single base substitutionGAmissense_variantG179R535G>A
MELA-AU157617576176175761single base substitutionGAmissense_variantG259R775G>A
MELA-AU157617576176175761single base substitutionGAmissense_variantG278R832G>A
MELA-AU157617576176175761single base substitutionGAmissense_variantG294R880G>A
MELA-AU157617632176176321single base substitutionCTintron_variant
MELA-AU157617673176176731single base substitutionCTintron_variant
MELA-AU157617679476176794single base substitutionCTintron_variant
MELA-AU157617736776177367single base substitutionCTintron_variant
MELA-AU157617854976178549single base substitutionCTintron_variant
MELA-AU157617857176178571single base substitutionCTintron_variant
MELA-AU157618014476180144single base substitutionTCintron_variant
MELA-AU157618114176181141single base substitutionCTintron_variant
MELA-AU157618122376181223single base substitutionCTintron_variant
MELA-AU157618151376181513single base substitutionGAintron_variant
MELA-AU157618166276181662single base substitutionTCintron_variant
MELA-AU157618206176182061single base substitutionCTintron_variant
MELA-AU157618215976182159single base substitutionCTintron_variant
MELA-AU157618226276182262single base substitutionCTintron_variant
MELA-AU157618227676182276single base substitutionCTintron_variant
MELA-AU157618467476184674single base substitutionTCintron_variant
MELA-AU157618494876184948single base substitutionCTintron_variant
MELA-AU157618558976185589single base substitutionTCintron_variant
MELA-AU157618597176185971single base substitutionCTintron_variant
MELA-AU157618601776186017single base substitutionCTintron_variant
MELA-AU157618684076186841multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU157618723176187231single base substitutionCTintron_variant
MELA-AU157618735976187359single base substitutionCTintron_variant
MELA-AU157618740976187409single base substitutionCTintron_variant
MELA-AU157618874376188743single base substitutionCTintron_variant
MELA-AU157618905676189056single base substitutionATintron_variant
MELA-AU157618930976189309single base substitutionGAintron_variant
MELA-AU157618967176189671single base substitutionCTdownstream_gene_variant
MELA-AU157618967176189671single base substitutionCTintron_variant
MELA-AU157619071176190711single base substitutionCTdownstream_gene_variant
MELA-AU157619071176190711single base substitutionCTintron_variant
MELA-AU157619105876191058single base substitutionCTdownstream_gene_variant
MELA-AU157619105876191058single base substitutionCTintron_variant
MELA-AU157619128276191282single base substitutionTGdownstream_gene_variant
MELA-AU157619128276191282single base substitutionTGintron_variant
MELA-AU157619134976191349single base substitutionCTdownstream_gene_variant
MELA-AU157619134976191349single base substitutionCTintron_variant
MELA-AU157619158376191583single base substitutionTAdownstream_gene_variant
MELA-AU157619158376191583single base substitutionTAintron_variant
MELA-AU157619161676191616insertion of <=200bp-Adownstream_gene_variant
MELA-AU157619161676191616insertion of <=200bp-Aintron_variant
MELA-AU157619248176192481single base substitutionCT3_prime_UTR_variant
MELA-AU157619248176192481single base substitutionCTdownstream_gene_variant
MELA-AU157619388176193881single base substitutionCTdownstream_gene_variant
MELA-AU157619419476194194single base substitutionCTdownstream_gene_variant
MELA-AU157619430376194303single base substitutionCTdownstream_gene_variant
MELA-AU157619482976194829single base substitutionCAdownstream_gene_variant
MELA-AU157619533576195335single base substitutionCTdownstream_gene_variant
MELA-AU157619572876195728single base substitutionATdownstream_gene_variant
MELA-AU157619628776196287single base substitutionCTdownstream_gene_variant
MELA-AU157619745276197453multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU157619818376198183single base substitutionATdownstream_gene_variant
ORCA-IN157614347076143470single base substitutionAGintron_variant
ORCA-IN157614929776149297deletion of <=200bpG-intron_variant
ORCA-IN157614929776149297deletion of <=200bpG-upstream_gene_variant
OV-AU157613125376131253single base substitutionCTupstream_gene_variant
OV-AU157613130276131302single base substitutionTAupstream_gene_variant
OV-AU157613439476134394single base substitutionGCupstream_gene_variant
OV-AU157613808576138085single base substitutionGCintron_variant
OV-AU157614279176142791single base substitutionGTintron_variant
OV-AU157615062076150620single base substitutionCTintron_variant
OV-AU157615062076150620single base substitutionCTupstream_gene_variant
OV-AU157615248376152483single base substitutionAGdownstream_gene_variant
OV-AU157615248376152483single base substitutionAGintron_variant
OV-AU157615488076154880single base substitutionGTdownstream_gene_variant
OV-AU157615488076154880single base substitutionGTintron_variant
OV-AU157615701476157014single base substitutionGCdownstream_gene_variant
OV-AU157615701476157014single base substitutionGCintron_variant
OV-AU157615701476157014single base substitutionGCupstream_gene_variant
OV-AU157616009976160099single base substitutionGCintron_variant
OV-AU157616009976160099single base substitutionGCupstream_gene_variant
OV-AU157616810376168103single base substitutionTCintron_variant
OV-AU157616810376168103single base substitutionTCupstream_gene_variant
OV-AU157616933376169333single base substitutionCTintron_variant
OV-AU157616933376169333single base substitutionCTupstream_gene_variant
OV-AU157617861076178610single base substitutionGAintron_variant
OV-AU157618735176187351single base substitutionCAintron_variant
OV-AU157619206776192067single base substitutionGC3_prime_UTR_variant
OV-AU157619206776192067single base substitutionGCdownstream_gene_variant
OV-AU157619722676197226single base substitutionGAdownstream_gene_variant
PACA-AU157613098676130986single base substitutionAGupstream_gene_variant
PACA-AU157613110776131107single base substitutionAGupstream_gene_variant
PACA-AU157613150476131504single base substitutionCTupstream_gene_variant
PACA-AU157614047276140472single base substitutionCAintron_variant
PACA-AU157614834676148346single base substitutionTCintron_variant
PACA-AU157614834676148346single base substitutionTCupstream_gene_variant
PACA-AU157614858776148587single base substitutionCTintron_variant
PACA-AU157614858776148587single base substitutionCTupstream_gene_variant
PACA-AU157614860876148608single base substitutionGAintron_variant
PACA-AU157614860876148608single base substitutionGAupstream_gene_variant
PACA-AU157614885476148854single base substitutionGCintron_variant
PACA-AU157614885476148854single base substitutionGCupstream_gene_variant
PACA-AU157615688976156889insertion of <=200bp-Tdownstream_gene_variant
PACA-AU157615688976156889insertion of <=200bp-Tintron_variant
PACA-AU157615688976156889insertion of <=200bp-Tupstream_gene_variant
PACA-AU157616764276167642single base substitutionCTintron_variant
PACA-AU157616764276167642single base substitutionCTupstream_gene_variant
PACA-AU157617244476172444single base substitutionTAintron_variant
PACA-AU157617981476179814single base substitutionCAintron_variant
PACA-AU157618118576181185single base substitutionTCintron_variant
PACA-AU157618956476189564insertion of <=200bp-Tdownstream_gene_variant
PACA-AU157618956476189564insertion of <=200bp-Tintron_variant
PACA-AU157619046276190474deletion of <=200bpTTTCATACTAAAC-downstream_gene_variant
PACA-AU157619046276190474deletion of <=200bpTTTCATACTAAAC-intron_variant
PACA-AU157619065376190653single base substitutionATdownstream_gene_variant
PACA-AU157619065376190653single base substitutionATintron_variant
PACA-AU157619409076194099deletion of <=200bpCTGGAGACCC-downstream_gene_variant
PACA-AU157619615876196158single base substitutionCAdownstream_gene_variant
PACA-CA157613144776131447single base substitutionTAupstream_gene_variant
PACA-CA157613165876131658single base substitutionTCupstream_gene_variant
PACA-CA157613293376132933single base substitutionCGupstream_gene_variant
PACA-CA157613655176136551insertion of <=200bp-GCGCA5_prime_UTR_variant
PACA-CA157613655176136551insertion of <=200bp-GCGCAexon_variant
PACA-CA157613655176136551insertion of <=200bp-GCGCAintron_variant
PACA-CA157613902276139022insertion of <=200bp-Aintron_variant
PACA-CA157614271076142710insertion of <=200bp-Tintron_variant
PACA-CA157614360676143606insertion of <=200bp-Tintron_variant
PACA-CA157614584576145845insertion of <=200bp-TATGintron_variant
PACA-CA157614598376145983single base substitutionCGintron_variant
PACA-CA157614661176146611deletion of <=200bpC-intron_variant
PACA-CA157614730776147307single base substitutionTGintron_variant
PACA-CA157614730776147307single base substitutionTGupstream_gene_variant
PACA-CA157614770176147701single base substitutionGAintron_variant
PACA-CA157614770176147701single base substitutionGAupstream_gene_variant
PACA-CA157614861476148614single base substitutionAGintron_variant
PACA-CA157614861476148614single base substitutionAGupstream_gene_variant
PACA-CA157615081076150810single base substitutionCAintron_variant
PACA-CA157615081076150810single base substitutionCAupstream_gene_variant
PACA-CA157615764876157648single base substitutionTCintron_variant
PACA-CA157615764876157648single base substitutionTCupstream_gene_variant
PACA-CA157615766876157668single base substitutionGAintron_variant
PACA-CA157615766876157668single base substitutionGAupstream_gene_variant
PACA-CA157615909976159099single base substitutionGTintron_variant
PACA-CA157615909976159099single base substitutionGTupstream_gene_variant
PACA-CA157615910976159109single base substitutionGTintron_variant
PACA-CA157615910976159109single base substitutionGTupstream_gene_variant
PACA-CA157615993876159938single base substitutionGTintron_variant
PACA-CA157615993876159938single base substitutionGTupstream_gene_variant
PACA-CA157616524276165242single base substitutionCTintron_variant
PACA-CA157616801376168013single base substitutionAGintron_variant
PACA-CA157616801376168013single base substitutionAGupstream_gene_variant
PACA-CA157617184376171843single base substitutionAGintron_variant
PACA-CA157617699376176993single base substitutionAGintron_variant
PACA-CA157617752276177522single base substitutionGAintron_variant
PACA-CA157618283876182838single base substitutionCTintron_variant
PACA-CA157618674476186744insertion of <=200bp-Aintron_variant
PACA-CA157618956376189563insertion of <=200bp-Tdownstream_gene_variant
PACA-CA157618956376189563insertion of <=200bp-Tintron_variant
PACA-CA157619542676195426single base substitutionCTdownstream_gene_variant
PACA-CA157619745876197458single base substitutionCTdownstream_gene_variant
PAEN-AU157613634476136344single base substitutionGCintron_variant
PAEN-AU157613634476136344single base substitutionGCupstream_gene_variant
PAEN-AU157613634776136347single base substitutionGCintron_variant
PAEN-AU157613634776136347single base substitutionGCupstream_gene_variant
PAEN-IT157613453776134537single base substitutionCAupstream_gene_variant
PAEN-IT157614564476145644single base substitutionCTintron_variant
PAEN-IT157616220876162208single base substitutionCAintron_variant
PBCA-DE157613783776137837single base substitutionGAintron_variant
PBCA-DE157615273276152732single base substitutionAGdownstream_gene_variant
PBCA-DE157615273276152732single base substitutionAGintron_variant
PBCA-DE157615278176152781single base substitutionTCdownstream_gene_variant
PBCA-DE157615278176152781single base substitutionTCintron_variant
PBCA-DE157615553676155536single base substitutionGAdownstream_gene_variant
PBCA-DE157615553676155536single base substitutionGAintron_variant
PBCA-DE157616237376162373deletion of <=200bpC-intron_variant
PBCA-DE157616457676164576insertion of <=200bp-Aintron_variant
PBCA-DE157616982176169821insertion of <=200bp-Aintron_variant
PBCA-DE157616982176169821insertion of <=200bp-Aupstream_gene_variant
PBCA-DE157617245476172454single base substitutionTGintron_variant
PBCA-DE157618985676189856single base substitutionCGdownstream_gene_variant
PBCA-DE157618985676189856single base substitutionCGintron_variant
PBCA-DE157619579076195790single base substitutionCTdownstream_gene_variant
PBCA-DE157619635576196355single base substitutionGAdownstream_gene_variant
PRAD-CA157613974776139747single base substitutionAGintron_variant
PRAD-CA157616774476167744single base substitutionTGintron_variant
PRAD-CA157616774476167744single base substitutionTGupstream_gene_variant
PRAD-CA157617482476174824single base substitutionGTintron_variant
PRAD-UK157614272176142721single base substitutionAGintron_variant
PRAD-UK157616855476168554single base substitutionTCintron_variant
PRAD-UK157616855476168554single base substitutionTCsynonymous_variantA170A510T>C
PRAD-UK157616855476168554single base substitutionTCsynonymous_variantA189A567T>C
PRAD-UK157616855476168554single base substitutionTCsynonymous_variantA205A615T>C
PRAD-UK157616855476168554single base substitutionTCsynonymous_variantA90A270T>C
PRAD-UK157616855476168554single base substitutionTCupstream_gene_variant
PRAD-UK157617052976170529single base substitutionGTexon_variant
PRAD-UK157617052976170529single base substitutionGTintron_variant
PRAD-UK157618419176184191single base substitutionGAintron_variant
PRAD-UK157619202376192023insertion of <=200bp-T3_prime_UTR_variant
PRAD-UK157619202376192023insertion of <=200bp-Tdownstream_gene_variant
READ-US157614677876146778single base substitutionACexon_variant
READ-US157614677876146778single base substitutionACmissense_variantN62H184A>C
READ-US157614677876146778single base substitutionACmissense_variantN78H232A>C
RECA-EU157613834876138348single base substitutionAGintron_variant
RECA-EU157614242676142426single base substitutionATintron_variant
RECA-EU157614898076148980single base substitutionCAintron_variant
RECA-EU157614898076148980single base substitutionCAupstream_gene_variant
RECA-EU157615013076150130single base substitutionTCintron_variant
RECA-EU157615013076150130single base substitutionTCupstream_gene_variant
RECA-EU157615455176154551single base substitutionACdownstream_gene_variant
RECA-EU157615455176154551single base substitutionACintron_variant
RECA-EU157615855076158550single base substitutionCTintron_variant
RECA-EU157615855076158550single base substitutionCTupstream_gene_variant
RECA-EU157616436276164362single base substitutionGTintron_variant
RECA-EU157616819776168197single base substitutionTGintron_variant
RECA-EU157616819776168197single base substitutionTGupstream_gene_variant
RECA-EU157616860176168601single base substitutionGAintron_variant
RECA-EU157616860176168601single base substitutionGAmissense_variantS106N317G>A
RECA-EU157616860176168601single base substitutionGAmissense_variantS186N557G>A
RECA-EU157616860176168601single base substitutionGAmissense_variantS205N614G>A
RECA-EU157616860176168601single base substitutionGAmissense_variantS221N662G>A
RECA-EU157616860176168601single base substitutionGAupstream_gene_variant
RECA-EU157617618276176182single base substitutionCTintron_variant
RECA-EU157617623376176233single base substitutionACintron_variant
RECA-EU157618923876189238single base substitutionCAintron_variant
SKCA-BR157613137976131379single base substitutionGAupstream_gene_variant
SKCA-BR157613243076132430single base substitutionGAupstream_gene_variant
SKCA-BR157613335276133352single base substitutionTCupstream_gene_variant
SKCA-BR157613363376133633single base substitutionGAupstream_gene_variant
SKCA-BR157613550976135509single base substitutionTCupstream_gene_variant
SKCA-BR157613566676135683deletion of <=200bpGAGCGCGCAGGGCGCGCC-5_prime_UTR_variant
SKCA-BR157613566676135683deletion of <=200bpGAGCGCGCAGGGCGCGCC-upstream_gene_variant
SKCA-BR157613631376136313single base substitutionTCintron_variant
SKCA-BR157613631376136313single base substitutionTCupstream_gene_variant
SKCA-BR157613644276136442single base substitutionCT5_prime_UTR_variant
SKCA-BR157613644276136442single base substitutionCTintron_variant
SKCA-BR157613644276136442single base substitutionCTupstream_gene_variant
SKCA-BR157613703076137030single base substitutionTGintron_variant
SKCA-BR157613952376139523single base substitutionTGintron_variant
SKCA-BR157614083976140839single base substitutionCTintron_variant
SKCA-BR157614646076146460single base substitutionTGintron_variant
SKCA-BR157614861276148612single base substitutionAGintron_variant
SKCA-BR157614861276148612single base substitutionAGupstream_gene_variant
SKCA-BR157615338276153382single base substitutionCTdownstream_gene_variant
SKCA-BR157615338276153382single base substitutionCTintron_variant
SKCA-BR157615584776155847single base substitutionCTdownstream_gene_variant
SKCA-BR157615584776155847single base substitutionCTintron_variant
SKCA-BR157615694876156948insertion of <=200bp-TAdownstream_gene_variant
SKCA-BR157615694876156948insertion of <=200bp-TAintron_variant
SKCA-BR157615694876156948insertion of <=200bp-TAupstream_gene_variant
SKCA-BR157616427776164277single base substitutionCTintron_variant
SKCA-BR157616671676166716single base substitutionCTintron_variant
SKCA-BR157616671676166716single base substitutionCTupstream_gene_variant
SKCA-BR157616840676168406insertion of <=200bp-CAAintron_variant
SKCA-BR157616840676168406insertion of <=200bp-CAAupstream_gene_variant
SKCA-BR157617054676170546single base substitutionGAexon_variant
SKCA-BR157617054676170546single base substitutionGAintron_variant
SKCA-BR157617802576178025single base substitutionCTintron_variant
SKCA-BR157618300976183009single base substitutionTAintron_variant
SKCA-BR157618301076183010single base substitutionCAintron_variant
SKCA-BR157618474076184740single base substitutionCTintron_variant
SKCA-BR157618634576186345single base substitutionTAintron_variant
SKCA-BR157618671176186711single base substitutionCTintron_variant
SKCA-BR157618671276186712single base substitutionCTintron_variant
SKCA-BR157618798476187984single base substitutionGAintron_variant
SKCA-BR157618979276189792single base substitutionCTdownstream_gene_variant
SKCA-BR157618979276189792single base substitutionCTintron_variant
SKCA-BR157619257576192575single base substitutionCT3_prime_UTR_variant
SKCA-BR157619257576192575single base substitutionCTdownstream_gene_variant
SKCA-BR157619523976195239single base substitutionAGdownstream_gene_variant
SKCA-BR157619553476195534single base substitutionCTdownstream_gene_variant
SKCA-BR157619579076195790single base substitutionCTdownstream_gene_variant
SKCA-BR157619731876197318single base substitutionCTdownstream_gene_variant
SKCM-US157614673176146731single base substitutionCTexon_variant
SKCM-US157614673176146731single base substitutionCTmissense_variantS46F137C>T
SKCM-US157614673176146731single base substitutionCTmissense_variantS62F185C>T
SKCM-US157617031176170311single base substitutionCTintron_variant
SKCM-US157617031176170311single base substitutionCTmissense_variantS113L338C>T
SKCM-US157617031176170311single base substitutionCTmissense_variantS193L578C>T
SKCM-US157617031176170311single base substitutionCTmissense_variantS212L635C>T
SKCM-US157617031176170311single base substitutionCTmissense_variantS228L683C>T
SKCM-US157617031176170311single base substitutionCTupstream_gene_variant
SKCM-US157617571676175716single base substitutionCTexon_variant
SKCM-US157617571676175716single base substitutionCTmissense_variantP164S490C>T
SKCM-US157617571676175716single base substitutionCTmissense_variantP244S730C>T
SKCM-US157617571676175716single base substitutionCTmissense_variantP263S787C>T
SKCM-US157617571676175716single base substitutionCTmissense_variantP279S835C>T
SKCM-US157617573776175737single base substitutionCTexon_variant
SKCM-US157617573776175737single base substitutionCTstop_gainedR171*511C>T
SKCM-US157617573776175737single base substitutionCTstop_gainedR251*751C>T
SKCM-US157617573776175737single base substitutionCTstop_gainedR270*808C>T
SKCM-US157617573776175737single base substitutionCTstop_gainedR286*856C>T
SKCM-US157619177976191779single base substitutionCT3_prime_UTR_variant
SKCM-US157619177976191779single base substitutionCTdownstream_gene_variant
SKCM-US157619177976191779single base substitutionCTmissense_variantP184L551C>T
SKCM-US157619177976191779single base substitutionCTmissense_variantP299L896C>T
SKCM-US157619177976191779single base substitutionCTmissense_variantP335S1003C>T
SKCM-US157619177976191779single base substitutionCTmissense_variantP354S1060C>T
SKCM-US157619177976191779single base substitutionCTmissense_variantP370S1108C>T
STAD-US157616133076161330single base substitutionAGexon_variant
STAD-US157616133076161330single base substitutionAGintron_variant
STAD-US157616133076161330single base substitutionAGsynonymous_variantE107E321A>G
STAD-US157616133076161330single base substitutionAGsynonymous_variantE126E378A>G
STAD-US157616133076161330single base substitutionAGsynonymous_variantE142E426A>G
STAD-US157616133076161330single base substitutionAGsynonymous_variantE27E81A>G
STAD-US157617036176170364deletion of <=200bpAAGT-frameshift_variantK130
STAD-US157617036176170364deletion of <=200bpAAGT-frameshift_variantK210
STAD-US157617036176170364deletion of <=200bpAAGT-frameshift_variantK229
STAD-US157617036176170364deletion of <=200bpAAGT-frameshift_variantK245
STAD-US157617036176170364deletion of <=200bpAAGT-intron_variant
STAD-US157617036176170364deletion of <=200bpAAGT-upstream_gene_variant
UCEC-US157616132876161330deletion of <=200bpGAA-exon_variant
UCEC-US157616132876161330deletion of <=200bpGAA-inframe_deletionE107
UCEC-US157616132876161330deletion of <=200bpGAA-inframe_deletionE126
UCEC-US157616132876161330deletion of <=200bpGAA-inframe_deletionE142
UCEC-US157616132876161330deletion of <=200bpGAA-inframe_deletionE27
UCEC-US157616132876161330deletion of <=200bpGAA-intron_variant
UCEC-US157616584476165844single base substitutionACexon_variant
UCEC-US157616584476165844single base substitutionACintron_variant
UCEC-US157616584476165844single base substitutionACmissense_variantI140L418A>C
UCEC-US157616584476165844single base substitutionACmissense_variantI159L475A>C
UCEC-US157616584476165844single base substitutionACmissense_variantI175L523A>C
UCEC-US157616584476165844single base substitutionACmissense_variantI60L178A>C
UCEC-US157616584476165844single base substitutionACupstream_gene_variant
UCEC-US157617144876171448single base substitutionTCexon_variant
UCEC-US157617144876171448single base substitutionTCintron_variant
UCEC-US157617144876171448single base substitutionTCsynonymous_variantP133P399T>C
UCEC-US157617144876171448single base substitutionTCsynonymous_variantP213P639T>C
UCEC-US157617144876171448single base substitutionTCsynonymous_variantP232P696T>C
UCEC-US157617144876171448single base substitutionTCsynonymous_variantP248P744T>C
UCEC-US157617573776175737single base substitutionCTexon_variant
UCEC-US157617573776175737single base substitutionCTstop_gainedR171*511C>T
UCEC-US157617573776175737single base substitutionCTstop_gainedR251*751C>T
UCEC-US157617573776175737single base substitutionCTstop_gainedR270*808C>T
UCEC-US157617573776175737single base substitutionCTstop_gainedR286*856C>T
UCEC-US157618328476183284single base substitutionGTexon_variant
UCEC-US157618328476183284single base substitutionGTintron_variant
UCEC-US157618328476183284single base substitutionGTstop_gainedE285*853G>T
UCEC-US157618328476183284single base substitutionGTstop_gainedE304*910G>T
UCEC-US157618328476183284single base substitutionGTstop_gainedE320*958G>T
UCEC-US157618328976183289single base substitutionGAexon_variant
UCEC-US157618328976183289single base substitutionGAintron_variant
UCEC-US157618328976183289single base substitutionGAsynonymous_variantS286S858G>A
UCEC-US157618328976183289single base substitutionGAsynonymous_variantS305S915G>A
UCEC-US157618328976183289single base substitutionGAsynonymous_variantS321S963G>A
UCEC-US157619177776191777single base substitutionCT3_prime_UTR_variant
UCEC-US157619177776191777single base substitutionCTdownstream_gene_variant
UCEC-US157619177776191777single base substitutionCTmissense_variantT334I1001C>T
UCEC-US157619177776191777single base substitutionCTmissense_variantT353I1058C>T
UCEC-US157619177776191777single base substitutionCTmissense_variantT369I1106C>T
UCEC-US157619177776191777single base substitutionCTsynonymous_variantH183H549C>T
UCEC-US157619177776191777single base substitutionCTsynonymous_variantH298H894C>T
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
IGROV-1COSM1678598c.74G>Ap.R25HSubstitution - Missense15:75843740-75843740+
2492709COSM5717818c.165C>Tp.L55LSubstitution - coding silent15:75843831-75843831+
HCC68COSM1608700c.915G>Tp.M305ISubstitution - Missense15:75890465-75890465+
TCGA-AP-A056-01COSM965076c.958G>Tp.E320*Substitution - Nonsense15:75890943-75890943+
TCGA-FW-A3R5-06COSM965075c.856C>Tp.R286*Substitution - Nonsense15:75883396-75883396+
40_FLCOSM4170726c.886T>Cp.Y296HSubstitution - Missense15:75890436-75890436+
TCGA-18-3408-01COSM701829c.319T>Cp.C107RSubstitution - Missense15:75859914-75859914+
TCGA-A8-A09B-01COSM434336c.203C>Tp.P68LSubstitution - Missense15:75854408-75854408+
STC252COSM1939665c.204G>Ap.P68PSubstitution - coding silent15:75854409-75854409+
SM-4B296COSM4409599c.825+2T>Ap.?Unknown15:75879190-75879190+
TCGA-AX-A05Z-01COSM965075c.856C>Tp.R286*Substitution - Nonsense15:75883396-75883396+
S02139COSM5674190c.757C>Tp.H253YSubstitution - Missense15:75879120-75879120+
CSCC-29-TCOSM4449946c.388-1G>Ap.?Unknown15:75868950-75868950+
TCGA-AA-3713-01COSM195972c.287G>Ap.R96HSubstitution - Missense15:75859882-75859882+
TCGA-D3-A51R-06COSM3504148c.1108C>Tp.P370SSubstitution - Missense15:75899438-75899438+
CCK81COSM1939681c.1063T>Cp.Y355HSubstitution - Missense15:75897028-75897028+
HT115COSM1939665c.204G>Ap.P68PSubstitution - coding silent15:75854409-75854409+
RK095_C01COSM3701012c.950A>Gp.Y317CSubstitution - Missense15:75890935-75890935+
4COSM5016493c.522delAp.I175fs*9Deletion - Frameshift15:75873502-75873502+
RMS66_COSM4988227c.460T>Gp.L154VSubstitution - Missense15:75873440-75873440+
BN03COSM3706742c.656C>Tp.S219LSubstitution - Missense15:75876254-75876254+
TCGA-IR-A3LA-01COSM4845654c.48C>Gp.I16MSubstitution - Missense15:75843714-75843714+
90COSM5015318c.40G>Cp.A14PSubstitution - Missense15:75843706-75843706+
TCGA-FW-A3TV-06COSM3504145c.185C>Tp.S62FSubstitution - Missense15:75854390-75854390+
LUAD-YINHDCOSM349101c.1097-1G>Tp.?Unknown15:75899426-75899426+
sysucc-783TCOSM5483959c.444T>Gp.A148ASubstitution - coding silent15:75869007-75869007+
Gp2DCOSM1939680c.1060T>Cp.S354PSubstitution - Missense15:75897025-75897025+
TCGA-D1-A174-01COSM965077c.963G>Ap.S321SSubstitution - coding silent15:75890948-75890948+
TCGA-F1-A448-01COSM4057028c.426A>Gp.E142ESubstitution - coding silent15:75868989-75868989+
T3056COSM4738708c.208T>Cp.W70RSubstitution - Missense15:75854413-75854413+
BN03TCOSM3706742c.656C>Tp.S219LSubstitution - Missense15:75876254-75876254+
C0017TCOSM4422488c.662G>Ap.S221NSubstitution - Missense15:75876260-75876260+
TCGA-AP-A059-01COSM965078c.1106C>Tp.T369ISubstitution - Missense15:75899436-75899436+
I2L-P19Ta-Tumor-OrganoidCOSM5362772c.826-7delTp.?Unknown15:75883359-75883359+
TCGA-25-1313-01COSM73180c.1112C>Gp.P371RSubstitution - Missense15:75899442-75899442+
B84COSM1749324c.599C>Ap.S200YSubstitution - Missense15:75876197-75876197+
YUKLABCOSM1708418c.836C>Tp.P279LSubstitution - Missense15:75883376-75883376+
HCC35TCOSM1608701c.1008A>Cp.R336SSubstitution - Missense15:75890993-75890993+
CSCC-56-TCOSM4481328c.24C>Tp.A8ASubstitution - coding silent15:75843690-75843690+
SNU-175COSM1939679c.1003G>Ap.A335TSubstitution - Missense15:75890988-75890988+
TCGA-29-2431-01COSM1323837c.846T>Cp.P282PSubstitution - coding silent15:75883386-75883386+
2492708COSM5717818c.165C>Tp.L55LSubstitution - coding silent15:75843831-75843831+
2492710COSM5717818c.165C>Tp.L55LSubstitution - coding silent15:75843831-75843831+
K136COSM249272c.51C>Ap.F17LSubstitution - Missense15:75843717-75843717+
RK262_C01COSM4778771c.194C>Tp.S65FSubstitution - Missense15:75854399-75854399+
TCGA-EE-A3AC-06COSM3504147c.835C>Tp.P279SSubstitution - Missense15:75883375-75883375+
SCMC_RM2_COSM4989342c.140A>Gp.H47RSubstitution - Missense15:75843806-75843806+
TCGA-CC-A3M9-01COSM4928602c.470A>Gp.Y157CSubstitution - Missense15:75873450-75873450+
TCGA-EB-A431-01COSM3504146c.683C>Tp.S228LSubstitution - Missense15:75877970-75877970+
TCGA-UB-A7MB-01COSM4931623c.293A>Tp.Q98LSubstitution - Missense15:75859888-75859888+
CSCC-11-TCOSM4547265c.418G>Ap.E140KSubstitution - Missense15:75868981-75868981+
Gp2DCOSM1939668c.304T>Cp.L102LSubstitution - coding silent15:75859899-75859899+
TCGA-B5-A11U-01COSM965072c.424_426delGAAp.E146delEDeletion - In frame15:75868987-75868989+
TCGA-AC-A23H-01COSM3816782c.289C>Gp.Q97ESubstitution - Missense15:75859884-75859884+
CSCC-31-TCOSM4555151c.643G>Ap.D215NSubstitution - Missense15:75876241-75876241+
TCGA-AA-3715-01COSM270489c.444T>Cp.A148ASubstitution - coding silent15:75869007-75869007+
TCGA-A5-A0GH-01COSM965074c.744T>Cp.P248PSubstitution - coding silent15:75879107-75879107+
TCGA-F5-6814-01COSM3420618c.232A>Cp.N78HSubstitution - Missense15:75854437-75854437+
Gp5DCOSM1939680c.1060T>Cp.S354PSubstitution - Missense15:75897025-75897025+
HCC68TCOSM1608700c.915G>Tp.M305ISubstitution - Missense15:75890465-75890465+
CSCC-55-TCOSM4547507c.424G>Ap.E142KSubstitution - Missense15:75868987-75868987+
90COSM5015319c.41C>Tp.A14VSubstitution - Missense15:75843707-75843707+
TCGA-AX-A05Z-01COSM965073c.523A>Cp.I175LSubstitution - Missense15:75873503-75873503+
TCGA-13-1501-01COSM69302c.448-1G>Tp.?Unknown15:75873427-75873427+
HCC35COSM1608701c.1008A>Cp.R336SSubstitution - Missense15:75890993-75890993+
YUKILCOSM1708417c.674_675GG>AAp.G225ESubstitution - Missense15:75877961-75877962+
TCGA-UB-A7MB-01COSM4931376c.1026T>Cp.N342NSubstitution - coding silent15:75891011-75891011+
Patient_1COSM5414129c.14G>Ap.G5ESubstitution - Missense15:75843680-75843680+
Gp5DCOSM1939668c.304T>Cp.L102LSubstitution - coding silent15:75859899-75859899+
ESCC_40COSM5629331c.909A>Gp.L303LSubstitution - coding silent15:75890459-75890459+
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.74041315q24.2612501
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
ATIntronicSNV.c.884+3342A>T1576179107CLL
CAMissensep.L292Ic.874C>A1576175755CM
CGMissensep.P371Rc.1112C>G1576191783OV
CTMissensep.P279Sc.835C>T1576175716CM
CTMissensep.P68Lc.203C>T1576146749BRCA
CTNonsensep.Q204*c.610C>T1576168549LUAD
GAA-InFrameDeletionp.E146delEc.435_437delAGA1576161328UCEC
GASpliceDonorSNV.c.673+1G>A1576168613LUAD
GASynonymousp.S321Sc.963G>A1576183289UCEC
GTSpliceAcceptorSNV.c.448-1G>T1576165768OV
TCMissensep.C107Rc.319T>C1576152255LUSC
TCSynonymousp.P248Pc.744T>C1576171448UCEC