TRIM6-TRIM34
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA1156558975655897+Nonsense_MutationSNPGGTTCGA-DK-A6AW-01A-11D-A30E-08TCGA-DK-A6AW-10A-01D-A30H-08g.chr11:5655897G>Tc.556G>Tc.(556-558)Gaa>Taap.E186*
BLCA1156560055656005+Missense_MutationSNPGGCTCGA-UY-A78O-01A-12D-A339-08TCGA-UY-A78O-10A-01D-A339-08g.chr11:5656005G>Cc.664G>Cc.(664-666)Gag>Cagp.E222Q
BLCA1156645435664543+Missense_MutationSNPGGCTCGA-BT-A20T-01A-11D-A14W-08TCGA-BT-A20T-11A-11D-A14W-08g.chr11:5664543G>Cc.1071G>Cc.(1069-1071)aaG>aaCp.K357N
BRCA1156536675653667+Nonsense_MutationSNPCCTTCGA-BH-A18G-01A-11D-A12B-09TCGA-BH-A18G-10A-01D-A12B-09g.chr11:5653667C>Tc.106C>Tc.(106-108)Cga>Tgap.R36*
BRCA1156550855655085+Missense_MutationSNPGGATCGA-AC-A3TM-01A-11D-A228-09TCGA-AC-A3TM-10A-01D-A22A-09g.chr11:5655085G>Ac.475G>Ac.(475-477)Gag>Aagp.E159K
CESC1156551305655130+Splice_SiteSNPGGTTCGA-EA-A439-01A-11D-A243-09TCGA-EA-A439-10A-01D-A243-09g.chr11:5655130G>Tc.e3+1
CESC1156559065655906+Missense_MutationSNPCCATCGA-C5-A1BQ-01C-11D-A20U-09TCGA-C5-A1BQ-10A-01D-A20U-09g.chr11:5655906C>Ac.565C>Ac.(565-567)Cag>Aagp.Q189K
COAD1156537225653722+Missense_MutationSNPGGTTCGA-AA-3811-01A-01W-0995-10TCGA-AA-3811-10A-01W-0995-10g.chr11:5653722G>Tc.161G>Tc.(160-162)aGc>aTcp.S54I
COAD1156537395653739+Missense_MutationSNPGGATCGA-G4-6293-01A-11D-1719-10TCGA-G4-6293-10A-01D-1719-10g.chr11:5653739G>Ac.178G>Ac.(178-180)Ggt>Agtp.G60S
COAD1156537395653739+Missense_MutationSNPGGTTCGA-D5-6533-01A-11D-1719-10TCGA-D5-6533-10A-01D-1719-10g.chr11:5653739G>Tc.178G>Tc.(178-180)Ggt>Tgtp.G60C
COAD1156537415653741+SilentSNPTTATCGA-CM-5868-01A-01D-1650-10TCGA-CM-5868-10A-01D-1650-10g.chr11:5653741T>Ac.180T>Ac.(178-180)ggT>ggAp.G60G
COAD1156537565653756+SilentSNPTTCTCGA-CM-4743-01A-01D-1719-10TCGA-CM-4743-10A-01D-1719-10g.chr11:5653756T>Cc.195T>Cc.(193-195)ttT>ttCp.F65F
COAD1156537685653768+SilentSNPGGATCGA-CM-5861-01A-01D-1650-10TCGA-CM-5861-10A-01D-1650-10g.chr11:5653768G>Ac.207G>Ac.(205-207)caG>caAp.Q69Q
COAD1156538825653882+Missense_MutationSNPCCATCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr11:5653882C>Ac.321C>Ac.(319-321)ttC>ttAp.F107L
COAD1156636555663655+Frame_Shift_DelDELAA-TCGA-CM-6674-01A-11D-1835-10TCGA-CM-6674-10A-01D-1835-10g.chr11:5663655delAc.793delAc.(793-795)aaafsp.K266fs
COAD1156636785663678+Missense_MutationSNPGGTTCGA-AA-3984-01A-02W-0995-10TCGA-AA-3984-10A-01W-0999-10g.chr11:5663678G>Tc.816G>Tc.(814-816)aaG>aaTp.K272N
COAD1156637385663738+Splice_SiteSNPTTCTCGA-DM-A1HB-01A-21D-A183-10TCGA-DM-A1HB-10A-01D-A183-10g.chr11:5663738T>Cc.e6+2
COAD1156645175664517+Missense_MutationSNPCCTTCGA-AA-A01Z-01A-11W-A096-10TCGA-AA-A01Z-11A-11W-A096-10g.chr11:5664517C>Tc.1045C>Tc.(1045-1047)Cat>Tatp.H349Y
COAD1156646595664659+Missense_MutationSNPGGTTCGA-AY-6196-01A-11D-1719-10TCGA-AY-6196-10A-01D-1719-10g.chr11:5664659G>Tc.1187G>Tc.(1186-1188)gGc>gTcp.G396V
COAD1156648105664810+Missense_MutationSNPTTGTCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr11:5664810T>Gc.1338T>Gc.(1336-1338)ttT>ttGp.F446L
COADREAD1156537225653722+Missense_MutationSNPGGTTCGA-AA-3811-01A-01W-0995-10TCGA-AA-3811-10A-01W-0995-10g.chr11:5653722G>Tc.161G>Tc.(160-162)aGc>aTcp.S54I
COADREAD1156537395653739+Missense_MutationSNPGGATCGA-G4-6293-01A-11D-1719-10TCGA-G4-6293-10A-01D-1719-10g.chr11:5653739G>Ac.178G>Ac.(178-180)Ggt>Agtp.G60S
COADREAD1156537395653739+Missense_MutationSNPGGTTCGA-D5-6533-01A-11D-1719-10TCGA-D5-6533-10A-01D-1719-10g.chr11:5653739G>Tc.178G>Tc.(178-180)Ggt>Tgtp.G60C
COADREAD1156537415653741+SilentSNPTTATCGA-CM-5868-01A-01D-1650-10TCGA-CM-5868-10A-01D-1650-10g.chr11:5653741T>Ac.180T>Ac.(178-180)ggT>ggAp.G60G
COADREAD1156537415653741+SilentSNPTTCTCGA-AG-3742-01A-11D-1657-10TCGA-AG-3742-11A-01D-1657-10g.chr11:5653741T>Cc.180T>Cc.(178-180)ggT>ggCp.G60G
COADREAD1156537565653756+SilentSNPTTCTCGA-CM-4743-01A-01D-1719-10TCGA-CM-4743-10A-01D-1719-10g.chr11:5653756T>Cc.195T>Cc.(193-195)ttT>ttCp.F65F
COADREAD1156537685653768+SilentSNPGGATCGA-CM-5861-01A-01D-1650-10TCGA-CM-5861-10A-01D-1650-10g.chr11:5653768G>Ac.207G>Ac.(205-207)caG>caAp.Q69Q
COADREAD1156538825653882+Missense_MutationSNPCCATCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr11:5653882C>Ac.321C>Ac.(319-321)ttC>ttAp.F107L
COADREAD1156636555663655+Frame_Shift_DelDELAA-TCGA-CM-6674-01A-11D-1835-10TCGA-CM-6674-10A-01D-1835-10g.chr11:5663655delAc.793delAc.(793-795)aaafsp.K266fs
COADREAD1156636785663678+Missense_MutationSNPGGTTCGA-AA-3984-01A-02W-0995-10TCGA-AA-3984-10A-01W-0999-10g.chr11:5663678G>Tc.816G>Tc.(814-816)aaG>aaTp.K272N
COADREAD1156637385663738+Splice_SiteSNPTTCTCGA-DM-A1HB-01A-21D-A183-10TCGA-DM-A1HB-10A-01D-A183-10g.chr11:5663738T>Cc.e6+2
COADREAD1156645175664517+Missense_MutationSNPCCTTCGA-AA-A01Z-01A-11W-A096-10TCGA-AA-A01Z-11A-11W-A096-10g.chr11:5664517C>Tc.1045C>Tc.(1045-1047)Cat>Tatp.H349Y
COADREAD1156646595664659+Missense_MutationSNPGGTTCGA-AY-6196-01A-11D-1719-10TCGA-AY-6196-10A-01D-1719-10g.chr11:5664659G>Tc.1187G>Tc.(1186-1188)gGc>gTcp.G396V
COADREAD1156648105664810+Missense_MutationSNPTTGTCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr11:5664810T>Gc.1338T>Gc.(1336-1338)ttT>ttGp.F446L
DLBC1156538665653866+Missense_MutationSNPAAGTCGA-G8-6909-01A-11D-2210-10TCGA-G8-6909-14A-01D-2210-10g.chr11:5653866A>Gc.305A>Gc.(304-306)gAg>gGgp.E102G
DLBC1156640475664047+Splice_SiteSNPAAGTCGA-FF-8042-01A-11D-2210-10TCGA-FF-8042-10A-01D-2210-10g.chr11:5664047A>Gc.875A>Gc.(874-876)gAa>gGap.E292G
ESCA1156558625655862+Splice_SiteSNPAATTCGA-LN-A8HZ-01A-11D-A36J-09TCGA-LN-A8HZ-10A-01D-A36M-09g.chr11:5655862A>Tc.521A>Tc.(520-522)tAt>tTtp.Y174F
ESCA1156559085655908+SilentSNPGGATCGA-Q9-A6FU-01A-11D-A31U-09TCGA-Q9-A6FU-10A-01D-A31U-09g.chr11:5655908G>Ac.567G>Ac.(565-567)caG>caAp.Q189Q
GBM1156560375656037+Missense_MutationSNPGGTTCGA-26-1442-01A-01D-1696-08TCGA-26-1442-10A-01D-1696-08g.chr11:5656037G>Tc.696G>Tc.(694-696)gaG>gaTp.E232D
GBMLGG1156559715655971+Missense_MutationSNPGGCTCGA-TM-A84Q-01A-11D-A36O-08TCGA-TM-A84Q-10A-01D-A367-08g.chr11:5655971G>Cc.630G>Cc.(628-630)aaG>aaCp.K210N
GBMLGG1156560375656037+Missense_MutationSNPGGTTCGA-26-1442-01A-01D-1696-08TCGA-26-1442-10A-01D-1696-08g.chr11:5656037G>Tc.696G>Tc.(694-696)gaG>gaTp.E232D
HNSC1156536055653605+Missense_MutationSNPGGATCGA-F7-A624-01A-22D-A30E-08TCGA-F7-A624-10A-01D-A30H-08g.chr11:5653605G>Ac.44G>Ac.(43-45)tGt>tAtp.C15Y
HNSC1156538895653889+Nonsense_MutationSNPGGTTCGA-CR-7371-01A-11D-2012-08TCGA-CR-7371-10A-01D-2013-08g.chr11:5653889G>Tc.328G>Tc.(328-330)Gag>Tagp.E110*
HNSC1156551055655105+SilentSNPCCATCGA-RS-A6TO-01A-32D-A34J-08TCGA-RS-A6TO-10A-01D-A34M-08g.chr11:5655105C>Ac.495C>Ac.(493-495)atC>atAp.I165I
HNSC1156558765655876+Missense_MutationSNPGGATCGA-F7-A624-01A-22D-A30E-08TCGA-F7-A624-10A-01D-A30H-08g.chr11:5655876G>Ac.535G>Ac.(535-537)Gag>Aagp.E179K
HNSC1156560915656091+Splice_SiteSNPGGCTCGA-CR-7388-01A-11D-2012-08TCGA-CR-7388-10A-01D-2013-08g.chr11:5656091G>Cc.750G>Cc.(748-750)caG>caCp.Q250H
HNSC1156648295664829+Missense_MutationSNPGGATCGA-BA-A6DI-01A-11D-A30E-08TCGA-BA-A6DI-10A-01D-A30H-08g.chr11:5664829G>Ac.1357G>Ac.(1357-1359)Ggc>Agcp.G453S
KICH1156551275655127+Missense_MutationSNPAAGTCGA-KN-8428-01A-11D-2310-10TCGA-KN-8428-11A-01D-2311-10g.chr11:5655127A>Gc.517A>Gc.(517-519)Aag>Gagp.K173E
KIPAN1156536475653647+Missense_MutationSNPAATTCGA-CZ-4862-01A-01D-1373-10TCGA-CZ-4862-11A-01D-1373-10g.chr11:5653647A>Tc.86A>Tc.(85-87)gAc>gTcp.D29V
KIPAN1156551275655127+Missense_MutationSNPAAGTCGA-KN-8428-01A-11D-2310-10TCGA-KN-8428-11A-01D-2311-10g.chr11:5655127A>Gc.517A>Gc.(517-519)Aag>Gagp.K173E
KIPAN1156551295655129+Splice_SiteSNPGGCTCGA-CJ-5676-01A-11D-1534-10TCGA-CJ-5676-11A-01D-1534-10g.chr11:5655129G>Cc.519G>Cc.(517-519)aaG>aaCp.K173N
KIRC1156536475653647+Missense_MutationSNPAATTCGA-CZ-4862-01A-01D-1373-10TCGA-CZ-4862-11A-01D-1373-10g.chr11:5653647A>Tc.86A>Tc.(85-87)gAc>gTcp.D29V
KIRC1156551295655129+Splice_SiteSNPGGCTCGA-CJ-5676-01A-11D-1534-10TCGA-CJ-5676-11A-01D-1534-10g.chr11:5655129G>Cc.519G>Cc.(517-519)aaG>aaCp.K173N
LGG1156559715655971+Missense_MutationSNPGGCTCGA-TM-A84Q-01A-11D-A36O-08TCGA-TM-A84Q-10A-01D-A367-08g.chr11:5655971G>Cc.630G>Cc.(628-630)aaG>aaCp.K210N
LIHC1156535725653572+Missense_MutationSNPAAGTCGA-DD-AAD3-01A-11D-A40R-10TCGA-DD-AAD3-10A-01D-A40U-10g.chr11:5653572A>Gc.11A>Gc.(10-12)aAa>aGap.K4R
LIHC1156647845664784+Missense_MutationSNPGGATCGA-G3-A3CG-01A-11D-A20W-10TCGA-G3-A3CG-10A-01D-A20W-10g.chr11:5664784G>Ac.1312G>Ac.(1312-1314)Gac>Aacp.D438N
LUAD1156536975653697+Missense_MutationSNPGGATCGA-05-4382-01A-01D-1931-08TCGA-05-4382-10A-01D-1265-08g.chr11:5653697G>Ac.136G>Ac.(136-138)Gca>Acap.A46T
LUAD1156550325655032+Splice_SiteSNPAATTCGA-17-Z045-01A-01W-0746-08TCGA-17-Z045-11A-01W-0747-08g.chr11:5655032A>Tc.e3-1
LUSC1156636375663637+Splice_SiteSNPAAGTCGA-56-6546-01A-11D-1817-08TCGA-56-6546-10A-01D-1817-08g.chr11:5663637A>Gc.775A>Gc.(775-777)Agt>Ggtp.S259G
LUSC1156648695664869+Missense_MutationSNPAATTCGA-34-5239-01A-21D-1817-08TCGA-34-5239-10A-01D-1817-08g.chr11:5664869A>Tc.1397A>Tc.(1396-1398)cAg>cTgp.Q466L
OV1156537395653739+Missense_MutationSNPGGCTCGA-09-2050-01A-01W-0799-08TCGA-09-2050-10A-01W-0799-08g.chr11:5653739G>Cc.178G>Cc.(178-180)Ggt>Cgtp.G60R
READ1156537415653741+SilentSNPTTCTCGA-AG-3742-01A-11D-1657-10TCGA-AG-3742-11A-01D-1657-10g.chr11:5653741T>Cc.180T>Cc.(178-180)ggT>ggCp.G60G
SKCM1156538725653872+Missense_MutationSNPTTGTCGA-EE-A181-06A-11D-A196-08TCGA-EE-A181-10A-01D-A198-08g.chr11:5653872T>Gc.311T>Gc.(310-312)cTc>cGcp.L104R
SKCM1156550335655033+Splice_SiteSNPGGATCGA-EE-A29L-06A-12D-A196-08TCGA-EE-A29L-10A-01D-A198-08g.chr11:5655033G>Ac.e3-1
SKCM1156550665655066+SilentSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr11:5655066G>Ac.456G>Ac.(454-456)aaG>aaAp.K152K
SKCM1156551145655114+SilentSNPGGATCGA-EE-A29D-06A-11D-A197-08TCGA-EE-A29D-10A-01D-A199-08g.chr11:5655114G>Ac.504G>Ac.(502-504)gaG>gaAp.E168E
SKCM1156640615664061+Missense_MutationSNPCCTTCGA-EE-A20C-06A-11D-A196-08TCGA-EE-A20C-10A-01D-A198-08g.chr11:5664061C>Tc.889C>Tc.(889-891)Cgg>Tggp.R297W
SKCM1156643875664387+SilentSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr11:5664387G>Ac.915G>Ac.(913-915)ctG>ctAp.L305L
SKCM1156644225664422+Missense_MutationSNPCCTTCGA-D3-A2JP-06A-11D-A19A-08TCGA-D3-A2JP-10A-01D-A19A-08g.chr11:5664422C>Tc.950C>Tc.(949-951)tCa>tTap.S317L
SKCM1156645315664531+SilentSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr11:5664531G>Ac.1059G>Ac.(1057-1059)gtG>gtAp.V353V
SKCM1156645845664584+Missense_MutationSNPCCTTCGA-FS-A1ZZ-06A-11D-A197-08TCGA-FS-A1ZZ-10A-01D-A199-08g.chr11:5664584C>Tc.1112C>Tc.(1111-1113)tCc>tTcp.S371F
SKCM1156647135664713+Missense_MutationSNPCCTTCGA-ER-A3PL-06A-11D-A23B-08TCGA-ER-A3PL-10A-01D-A23B-08g.chr11:5664713C>Tc.1241C>Tc.(1240-1242)tCt>tTtp.S414F
SKCM1156647465664746+Missense_MutationSNPCCTTCGA-D3-A2JH-06A-11D-A196-08TCGA-D3-A2JH-10A-01D-A198-08g.chr11:5664746C>Tc.1274C>Tc.(1273-1275)tCc>tTcp.S425F
SKCM1156647475664747+SilentSNPCCTTCGA-D3-A2JH-06A-11D-A196-08TCGA-D3-A2JH-10A-01D-A198-08g.chr11:5664747C>Tc.1275C>Tc.(1273-1275)tcC>tcTp.S425S
SKCM1156647475664747+SilentSNPCCTTCGA-ER-A42L-06A-11D-A24R-08TCGA-ER-A42L-10A-01D-A24R-08g.chr11:5664747C>Tc.1275C>Tc.(1273-1275)tcC>tcTp.S425S
SKCM1156648135664813+SilentSNPCCTTCGA-EE-A3J5-06A-11D-A20D-08TCGA-EE-A3J5-10A-01D-A20D-08g.chr11:5664813C>Tc.1341C>Tc.(1339-1341)ttC>ttTp.F447F
BLCA1156534965653496+5'UTRSNPTTCTCGA-ZF-A9RF-01A-11D-A38G-08TCGA-ZF-A9RF-10A-01D-A38J-08g.chr11:5653496T>C
COAD1156535465653546+5'UTRSNPCCTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr11:5653546C>T
COAD1156535465653546+5'UTRSNPCCTTCGA-AD-6964-01A-11D-1924-10TCGA-AD-6964-10A-01D-1924-10g.chr11:5653546C>T
COADREAD1156535465653546+5'UTRSNPCCTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr11:5653546C>T
COADREAD1156535465653546+5'UTRSNPCCTTCGA-AD-6964-01A-11D-1924-10TCGA-AD-6964-10A-01D-1924-10g.chr11:5653546C>T
HNSC1156534925653492+5'UTRDELGG-TCGA-F7-A624-01A-22D-A30E-08TCGA-F7-A624-10A-01D-A30H-08g.chr11:5653492delG
SKCM1156535155653515+5'UTRSNPGGATCGA-GN-A4U3-06A-11D-A32N-08TCGA-GN-A4U3-10F-01D-A32N-08g.chr11:5653515G>A
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
AML-US1156317815631781single base substitutionAGsynonymous_variantQ325Q975A>G
BLCA-CN1156246655624665single base substitutionACsynonymous_variantP69P207A>C
BLCA-CN1156325625632562single base substitutionCAintron_variant
BLCA-CN1156637065663706single base substitutionGCmissense_variantD282H844G>C
BLCA-CN1156637065663706single base substitutionGCmissense_variantD636H1906G>C
BLCA-US1156244765624476single base substitutionGAsplice_region_variant
BLCA-US1156248605624860single base substitutionCGsynonymous_variantL134L402C>G
BLCA-US1156645435664543single base substitutionGCmissense_variantK357N1071G>C
BLCA-US1156645435664543single base substitutionGCmissense_variantK711N2133G>C
BRCA-EU1156138665613866single base substitutionGAupstream_gene_variant
BRCA-EU1156139155613915single base substitutionAGupstream_gene_variant
BRCA-EU1156149925614992single base substitutionGCupstream_gene_variant
BRCA-EU1156158425615842deletion of <=200bpT-upstream_gene_variant
BRCA-EU1156169655616965single base substitutionTAupstream_gene_variant
BRCA-EU1156187705618770deletion of <=200bpA-intron_variant
BRCA-EU1156190825619082single base substitutionGAintron_variant
BRCA-EU1156204085620408single base substitutionTGintron_variant
BRCA-EU1156207375620737single base substitutionCAintron_variant
BRCA-EU1156211545621154single base substitutionAGintron_variant
BRCA-EU1156220795622079single base substitutionGCintron_variant
BRCA-EU1156228395622839deletion of <=200bpT-intron_variant
BRCA-EU1156231555623155single base substitutionGCintron_variant
BRCA-EU1156249045624904single base substitutionGAmissense_variantR149Q446G>A
BRCA-EU1156252935625293single base substitutionCTintron_variant
BRCA-EU1156259285625980deletion of <=200bpAGGAGTCCTTGTCCTGTCTGTCCTCTGATGCCATGACTAGAAGAGCTTCCCTT-intron_variant
BRCA-EU1156279625627962single base substitutionGAintron_variant
BRCA-EU1156294035629403single base substitutionAGintron_variant
BRCA-EU1156304535630453single base substitutionAGintron_variant
BRCA-EU1156315635631563single base substitutionGAintron_variant
BRCA-EU1156346165634616single base substitutionTCintron_variant
BRCA-EU1156350465635046single base substitutionGTintron_variant
BRCA-EU1156355025635502single base substitutionGCintron_variant
BRCA-EU1156360015636001deletion of <=200bpT-intron_variant
BRCA-EU1156366635636663single base substitutionTCintron_variant
BRCA-EU1156373475637347single base substitutionATintron_variant
BRCA-EU1156375765637576single base substitutionGAintron_variant
BRCA-EU1156432485643248single base substitutionTCintron_variant
BRCA-EU1156433305643330single base substitutionGTintron_variant
BRCA-EU1156456215645621single base substitutionCGintron_variant
BRCA-EU1156471925647192single base substitutionGCintron_variant
BRCA-EU1156482945648294single base substitutionGAintron_variant
BRCA-EU1156491915649191single base substitutionTAintron_variant
BRCA-EU1156491915649191single base substitutionTAupstream_gene_variant
BRCA-EU1156499515649951single base substitutionCTintron_variant
BRCA-EU1156499515649951single base substitutionCTupstream_gene_variant
BRCA-EU1156518775651877single base substitutionTCintron_variant
BRCA-EU1156518775651877single base substitutionTCupstream_gene_variant
BRCA-EU1156519135651913single base substitutionATintron_variant
BRCA-EU1156519135651913single base substitutionATupstream_gene_variant
BRCA-EU1156525695652569single base substitutionGCintron_variant
BRCA-EU1156525695652569single base substitutionGCupstream_gene_variant
BRCA-EU1156527545652754single base substitutionGAintron_variant
BRCA-EU1156527545652754single base substitutionGAupstream_gene_variant
BRCA-EU1156542565654256single base substitutionGCintron_variant
BRCA-EU1156563945656394single base substitutionCTintron_variant
BRCA-EU1156568025656802single base substitutionTAintron_variant
BRCA-EU1156623115662311insertion of <=200bp-Tintron_variant
BRCA-EU1156623195662319deletion of <=200bpC-intron_variant
BRCA-EU1156623395662339single base substitutionCTintron_variant
BRCA-EU1156630845663085deletion of <=200bpTT-intron_variant
BRCA-EU1156640055664005single base substitutionCAintron_variant
BRCA-EU1156682135668213single base substitutionACdownstream_gene_variant
BRCA-EU1156688515668851single base substitutionCTdownstream_gene_variant
BRCA-EU1156695635669563single base substitutionCTdownstream_gene_variant
BRCA-FR1156204085620408single base substitutionTGintron_variant
BRCA-FR1156279625627962single base substitutionGAintron_variant
BRCA-FR1156366635636663single base substitutionTCintron_variant
BRCA-FR1156471925647192single base substitutionGCintron_variant
BRCA-FR1156620375662037single base substitutionCTintron_variant
BRCA-UK1156538635653863single base substitutionGCmissense_variantG101A302G>C
BRCA-UK1156538635653863single base substitutionGCmissense_variantG455A1364G>C
BRCA-US1156179875617987single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
BRCA-US1156180775618077single base substitutionGC5_prime_UTR_variant
BRCA-US1156244975624497single base substitutionCGmissense_variantI13M39C>G
BRCA-US1156246075624607single base substitutionTAmissense_variantL50Q149T>A
BRCA-US1156247315624731single base substitutionCGstop_gainedY91*273C>G
BRCA-US1156267215626721single base substitutionACmissense_variantH253P758A>C
BRCA-US1156314315631431single base substitutionTAmissense_variantM305K914T>A
BRCA-US1156322995632299single base substitutionGCintron_variant
BRCA-US1156323045632304single base substitutionGAintron_variant
BRCA-US1156323995632399single base substitutionCTintron_variant
BRCA-US1156536675653667single base substitutionCTstop_gainedR36*106C>T
BRCA-US1156536675653667single base substitutionCTstop_gainedR390*1168C>T
BTCA-JP1156247805624780single base substitutionCTmissense_variantR108W322C>T
BTCA-JP1156247895624789single base substitutionGAmissense_variantE111K331G>A
BTCA-JP1156257995625799single base substitutionCTsynonymous_variantN181N543C>T
BTCA-JP1156557625655762single base substitutionTCintron_variant
BTCA-JP1156624235662423single base substitutionCTsplice_region_variant
BTCA-JP1156640205664020single base substitutionGAintron_variant
BTCA-JP1156646265664626single base substitutionAGmissense_variantQ385R1154A>G
BTCA-JP1156646265664626single base substitutionAGmissense_variantQ739R2216A>G
CESC-US1156244765624476single base substitutionGAsplice_region_variant
CESC-US1156551305655130single base substitutionGTsplice_donor_variant
CESC-US1156559065655906single base substitutionCAmissense_variantQ189K565C>A
CESC-US1156559065655906single base substitutionCAmissense_variantQ543K1627C>A
COAD-US1156257625625764deletion of <=200bpAGG-frameshift_variantQE170
COAD-US1156266185626618single base substitutionCTstop_gainedR219*655C>T
COAD-US1156266735626675deletion of <=200bpAGA-inframe_deletionEK237E
COAD-US1156320185632018single base substitutionCAintron_variant
COAD-US1156535465653546single base substitutionCTsynonymous_variantS349S1047C>T
COAD-US1156535465653546single base substitutionCTupstream_gene_variant
COAD-US1156537565653756single base substitutionTCsynonymous_variantF419F1257T>C
COAD-US1156537565653756single base substitutionTCsynonymous_variantF65F195T>C
COAD-US1156537685653768single base substitutionGAsynonymous_variantQ423Q1269G>A
COAD-US1156537685653768single base substitutionGAsynonymous_variantQ69Q207G>A
COAD-US1156624115662411single base substitutionCAsynonymous_variantI255I765C>A
COAD-US1156624115662411single base substitutionCAsynonymous_variantI609I1827C>A
COAD-US1156624495662449insertion of <=200bp-Tintron_variant
COAD-US1156636555663655deletion of <=200bpA-frameshift_variantK265
COAD-US1156636555663655deletion of <=200bpA-frameshift_variantK619
COAD-US1156646595664659single base substitutionGTmissense_variantG396V1187G>T
COAD-US1156646595664659single base substitutionGTmissense_variantG750V2249G>T
COAD-US1156646845664684single base substitutionTGmissense_variantN404K1212T>G
COAD-US1156646845664684single base substitutionTGmissense_variantN758K2274T>G
COAD-US1156648315664831single base substitutionCAsynonymous_variantG453G1359C>A
COAD-US1156648315664831single base substitutionCAsynonymous_variantG807G2421C>A
COCA-CN1156140625614062single base substitutionAGupstream_gene_variant
COCA-CN1156141365614136single base substitutionGTupstream_gene_variant
COCA-CN1156181155618115single base substitutionTC5_prime_UTR_variant
COCA-CN1156252515625251single base substitutionCTintron_variant
COCA-CN1156257605625760single base substitutionCAsplice_region_variant
COCA-CN1156258175625817single base substitutionGTmissense_variantE187D561G>T
COCA-CN1156258285625828single base substitutionCTmissense_variantA191V572C>T
COCA-CN1156258935625893single base substitutionCTintron_variant
COCA-CN1156267635626763single base substitutionGAmissense_variantR267H800G>A
COCA-CN1156313515631351single base substitutionAGintron_variant
COCA-CN1156313845631384single base substitutionCAmissense_variantF289L867C>A
COCA-CN1156315535631553single base substitutionCTintron_variant
COCA-CN1156317605631760single base substitutionTCsplice_region_variant
COCA-CN1156322295632229single base substitutionCAintron_variant
COCA-CN1156325515632551single base substitutionCTintron_variant
COCA-CN1156326955632695single base substitutionCAintron_variant
COCA-CN1156327235632723single base substitutionGAintron_variant
COCA-CN1156327305632730single base substitutionCTintron_variant
COCA-CN1156387815638781single base substitutionCTintron_variant
COCA-CN1156388215638821single base substitutionCTintron_variant
COCA-CN1156422155642215single base substitutionTCintron_variant
COCA-CN1156557585655758single base substitutionCTintron_variant
COCA-CN1156557605655760single base substitutionCTintron_variant
COCA-CN1156558625655862single base substitutionAGmissense_variantY174C521A>G
COCA-CN1156558625655862single base substitutionAGmissense_variantY528C1583A>G
COCA-CN1156643575664357single base substitutionTAintron_variant
EOPC-DE1156154165615416single base substitutionCTupstream_gene_variant
EOPC-DE1156262125626212single base substitutionGAintron_variant
EOPC-DE1156263145626314single base substitutionCTintron_variant
ESAD-UK1156131895613189single base substitutionTCupstream_gene_variant
ESAD-UK1156139395613939single base substitutionGCupstream_gene_variant
ESAD-UK1156147635614763insertion of <=200bp-Tupstream_gene_variant
ESAD-UK1156151355615135single base substitutionCTupstream_gene_variant
ESAD-UK1156155805615580single base substitutionCTupstream_gene_variant
ESAD-UK1156156465615646single base substitutionTCupstream_gene_variant
ESAD-UK1156157575615757single base substitutionACupstream_gene_variant
ESAD-UK1156189785618978single base substitutionGAintron_variant
ESAD-UK1156204295620429single base substitutionAGintron_variant
ESAD-UK1156205625620562single base substitutionGAintron_variant
ESAD-UK1156209725620972single base substitutionGTintron_variant
ESAD-UK1156215165621516single base substitutionCGintron_variant
ESAD-UK1156236515623651single base substitutionCTintron_variant
ESAD-UK1156237075623707single base substitutionTCintron_variant
ESAD-UK1156239385623938single base substitutionCTintron_variant
ESAD-UK1156263235626323single base substitutionGTintron_variant
ESAD-UK1156264635626463single base substitutionGTintron_variant
ESAD-UK1156285235628523single base substitutionAGintron_variant
ESAD-UK1156287235628723single base substitutionTGintron_variant
ESAD-UK1156297265629726single base substitutionCAintron_variant
ESAD-UK1156297275629727single base substitutionACintron_variant
ESAD-UK1156306275630627single base substitutionCAintron_variant
ESAD-UK1156312395631239single base substitutionCAintron_variant
ESAD-UK1156315425631542single base substitutionGAintron_variant
ESAD-UK1156324145632414single base substitutionTGintron_variant
ESAD-UK1156325915632591single base substitutionCTintron_variant
ESAD-UK1156331035633103single base substitutionGAintron_variant
ESAD-UK1156331365633136single base substitutionTAintron_variant
ESAD-UK1156334505633450single base substitutionGTintron_variant
ESAD-UK1156339065633906single base substitutionAGintron_variant
ESAD-UK1156346295634629single base substitutionTCintron_variant
ESAD-UK1156356545635654single base substitutionCTintron_variant
ESAD-UK1156358415635841single base substitutionCTintron_variant
ESAD-UK1156370745637074single base substitutionCTintron_variant
ESAD-UK1156390005639000single base substitutionTGintron_variant
ESAD-UK1156390775639077single base substitutionATintron_variant
ESAD-UK1156391275639127single base substitutionGAintron_variant
ESAD-UK1156448575644857single base substitutionGAintron_variant
ESAD-UK1156461975646197single base substitutionGAintron_variant
ESAD-UK1156510905651090single base substitutionGAintron_variant
ESAD-UK1156510905651090single base substitutionGAupstream_gene_variant
ESAD-UK1156512975651297single base substitutionCTintron_variant
ESAD-UK1156512975651297single base substitutionCTupstream_gene_variant
ESAD-UK1156513655651365single base substitutionGAintron_variant
ESAD-UK1156513655651365single base substitutionGAupstream_gene_variant
ESAD-UK1156513925651392single base substitutionATintron_variant
ESAD-UK1156513925651392single base substitutionATupstream_gene_variant
ESAD-UK1156515215651521deletion of <=200bpT-intron_variant
ESAD-UK1156515215651521deletion of <=200bpT-upstream_gene_variant
ESAD-UK1156536145653614single base substitutionGCmissense_variantC18S53G>C
ESAD-UK1156536145653614single base substitutionGCmissense_variantC372S1115G>C
ESAD-UK1156547555654755single base substitutionCGintron_variant
ESAD-UK1156560195656019single base substitutionGAsynonymous_variantQ226Q678G>A
ESAD-UK1156560195656019single base substitutionGAsynonymous_variantQ580Q1740G>A
ESAD-UK1156579045657904single base substitutionTGintron_variant
ESAD-UK1156588535658853single base substitutionCAintron_variant
ESAD-UK1156593665659366single base substitutionCAintron_variant
ESAD-UK1156595475659547single base substitutionGCintron_variant
ESAD-UK1156601075660107single base substitutionAGintron_variant
ESAD-UK1156603605660360single base substitutionGAintron_variant
ESAD-UK1156614965661496single base substitutionTCintron_variant
ESAD-UK1156619435661943single base substitutionGTintron_variant
ESAD-UK1156640615664061single base substitutionCTmissense_variantR297W889C>T
ESAD-UK1156640615664061single base substitutionCTmissense_variantR651W1951C>T
ESAD-UK1156643455664345insertion of <=200bp-ATATATintron_variant
ESAD-UK1156644395664439single base substitutionGAmissense_variantV323M967G>A
ESAD-UK1156644395664439single base substitutionGAmissense_variantV677M2029G>A
ESAD-UK1156658785665878single base substitutionCTdownstream_gene_variant
ESAD-UK1156671085667108single base substitutionATdownstream_gene_variant
ESAD-UK1156681675668167deletion of <=200bpA-downstream_gene_variant
ESAD-UK1156681675668167insertion of <=200bp-Adownstream_gene_variant
ESAD-UK1156688205668820single base substitutionTCdownstream_gene_variant
ESAD-UK1156690045669004single base substitutionGAdownstream_gene_variant
ESAD-UK1156694235669423single base substitutionAGdownstream_gene_variant
ESAD-UK1156697555669755deletion of <=200bpA-downstream_gene_variant
ESCA-CN1156267335626733single base substitutionCTmissense_variantS257L770C>T
GBM-US1156258495625849single base substitutionCAmissense_variantT198K593C>A
GBM-US1156266455626645single base substitutionCTmissense_variantR228W682C>T
GBM-US1156314065631406single base substitutionGAmissense_variantA297T889G>A
GBM-US1156560375656037single base substitutionGTmissense_variantE232D696G>T
GBM-US1156560375656037single base substitutionGTmissense_variantE586D1758G>T
KIRC-US1156249335624933single base substitutionTGmissense_variantF159V475T>G
KIRC-US1156249415624943deletion of <=200bpGGA-inframe_deletionVE161V
KIRC-US1156322135632213single base substitutionGAintron_variant
KIRC-US1156536475653647single base substitutionATmissense_variantD29V86A>T
KIRC-US1156536475653647single base substitutionATmissense_variantD383V1148A>T
KIRC-US1156551295655129single base substitutionGCmissense_variantK173N519G>C
KIRC-US1156551295655129single base substitutionGCmissense_variantK527N1581G>C
LAML-KR1156265005626500single base substitutionCTintron_variant
LAML-KR1156370995637099single base substitutionCAintron_variant
LAML-KR1156635755663575single base substitutionTCintron_variant
LGG-US1156245325624532single base substitutionGAmissense_variantR25K74G>A
LICA-CN1156267715626771single base substitutionCTstop_gainedQ270*808C>T
LICA-CN1156559465655946single base substitutionTAmissense_variantL202Q605T>A
LICA-CN1156559465655946single base substitutionTAmissense_variantL556Q1667T>A
LICA-FR1156247165624716single base substitutionGAsynonymous_variantV86V258G>A
LICA-FR1156248495624849single base substitutionACmissense_variantK131Q391A>C
LICA-FR1156320635632063single base substitutionCTintron_variant
LICA-FR1156413975641397single base substitutionCTintron_variant
LICA-FR1156497255649725single base substitutionCTintron_variant
LICA-FR1156497255649725single base substitutionCTupstream_gene_variant
LICA-FR1156539595653959single base substitutionCTmissense_variantT133M398C>T
LICA-FR1156539595653959single base substitutionCTmissense_variantT487M1460C>T
LICA-FR1156556865655686single base substitutionTCintron_variant
LICA-FR1156557625655762single base substitutionTCintron_variant
LIHC-US1156247715624771single base substitutionAGmissense_variantI105V313A>G
LIHC-US1156636725663672single base substitutionTCsynonymous_variantV270V810T>C
LIHC-US1156636725663672single base substitutionTCsynonymous_variantV624V1872T>C
LINC-JP1156183045618304single base substitutionATintron_variant
LINC-JP1156244515624451single base substitutionTAintron_variant
LINC-JP1156245815624581single base substitutionGTsynonymous_variantV41V123G>T
LINC-JP1156280615628061single base substitutionAGintron_variant
LINC-JP1156438105643810single base substitutionTAintron_variant
LINC-JP1156447835644783single base substitutionGTintron_variant
LINC-JP1156557605655760single base substitutionCTintron_variant
LINC-JP1156650075665007single base substitutionAG3_prime_UTR_variant
LINC-JP1156672875667287single base substitutionGAdownstream_gene_variant
LIRI-JP1156136955613695single base substitutionGAupstream_gene_variant
LIRI-JP1156153515615351single base substitutionTCupstream_gene_variant
LIRI-JP1156216035621603single base substitutionTGintron_variant
LIRI-JP1156281175628117single base substitutionGTintron_variant
LIRI-JP1156303025630302single base substitutionTCintron_variant
LIRI-JP1156312015631201single base substitutionTCintron_variant
LIRI-JP1156326675632667single base substitutionTGintron_variant
LIRI-JP1156330195633019single base substitutionTCintron_variant
LIRI-JP1156340305634030single base substitutionTCintron_variant
LIRI-JP1156358465635846single base substitutionAGintron_variant
LIRI-JP1156388835638883single base substitutionTCintron_variant
LIRI-JP1156398085639808single base substitutionGTintron_variant
LIRI-JP1156401785640178single base substitutionTCintron_variant
LIRI-JP1156407215640721single base substitutionTCintron_variant
LIRI-JP1156436475643647single base substitutionCTintron_variant
LIRI-JP1156436645643664single base substitutionGAintron_variant
LIRI-JP1156440185644018single base substitutionTCintron_variant
LIRI-JP1156455225645522single base substitutionCGintron_variant
LIRI-JP1156469955646995single base substitutionTCintron_variant
LIRI-JP1156503575650357single base substitutionAGintron_variant
LIRI-JP1156503575650357single base substitutionAGupstream_gene_variant
LIRI-JP1156509255650925single base substitutionGAintron_variant
LIRI-JP1156509255650925single base substitutionGAupstream_gene_variant
LIRI-JP1156511885651188single base substitutionGAintron_variant
LIRI-JP1156511885651188single base substitutionGAupstream_gene_variant
LIRI-JP1156512985651298single base substitutionGAintron_variant
LIRI-JP1156512985651298single base substitutionGAupstream_gene_variant
LIRI-JP1156530525653052single base substitutionGCintron_variant
LIRI-JP1156530525653052single base substitutionGCupstream_gene_variant
LIRI-JP1156552425655242single base substitutionTGintron_variant
LIRI-JP1156565805656580single base substitutionGTintron_variant
LIRI-JP1156611035661103single base substitutionGTintron_variant
LIRI-JP1156634975663497single base substitutionCAintron_variant
LIRI-JP1156642545664254single base substitutionCTintron_variant
LIRI-JP1156643375664337single base substitutionTAintron_variant
LIRI-JP1156659305665930single base substitutionGAdownstream_gene_variant
LIRI-JP1156665535666553single base substitutionCTdownstream_gene_variant
LIRI-JP1156678855667885single base substitutionAGdownstream_gene_variant
LUSC-KR1156150195615019single base substitutionGTupstream_gene_variant
LUSC-KR1156177125617712single base substitutionAGupstream_gene_variant
LUSC-KR1156237375623737single base substitutionCAintron_variant
LUSC-KR1156245935624593single base substitutionCTsynonymous_variantI45I135C>T
LUSC-KR1156258965625896single base substitutionGCintron_variant
LUSC-KR1156336005633600single base substitutionAGintron_variant
LUSC-KR1156336895633689single base substitutionAGintron_variant
LUSC-KR1156337475633747single base substitutionCTintron_variant
LUSC-KR1156340455634045single base substitutionTAintron_variant
LUSC-KR1156533255653325single base substitutionCAintron_variant
LUSC-KR1156533255653325single base substitutionCAupstream_gene_variant
LUSC-KR1156557605655760single base substitutionCTintron_variant
LUSC-KR1156557625655762single base substitutionTCintron_variant
LUSC-KR1156578915657891single base substitutionATintron_variant
LUSC-KR1156647975664797single base substitutionGAmissense_variantG442D1325G>A
LUSC-KR1156647975664797single base substitutionGAmissense_variantG796D2387G>A
LUSC-US1156267905626790single base substitutionTAmissense_variantL276Q827T>A
LUSC-US1156325165632516single base substitutionTCintron_variant
LUSC-US1156636375663637single base substitutionAGmissense_variantS259G775A>G
LUSC-US1156636375663637single base substitutionAGmissense_variantS613G1837A>G
LUSC-US1156648695664869single base substitutionATmissense_variantQ466L1397A>T
LUSC-US1156648695664869single base substitutionATmissense_variantQ820L2459A>T
MALY-DE1156143815614381single base substitutionTGupstream_gene_variant
MALY-DE1156161675616167single base substitutionTCupstream_gene_variant
MALY-DE1156184645618464single base substitutionCTintron_variant
MALY-DE1156187705618770deletion of <=200bpA-intron_variant
MALY-DE1156194635619463single base substitutionTAintron_variant
MALY-DE1156211945621194single base substitutionGTintron_variant
MALY-DE1156284345628434insertion of <=200bp-Aintron_variant
MALY-DE1156327535632753single base substitutionGAintron_variant
MALY-DE1156346605634660single base substitutionGAintron_variant
MALY-DE1156386195638619single base substitutionAGintron_variant
MALY-DE1156481295648129single base substitutionAGintron_variant
MALY-DE1156487365648737deletion of <=200bpTT-intron_variant
MALY-DE1156487365648737deletion of <=200bpTT-upstream_gene_variant
MALY-DE1156564775656477single base substitutionCTintron_variant
MALY-DE1156643755664375single base substitutionGAsplice_region_variant
MALY-DE1156665545666554single base substitutionGAdownstream_gene_variant
MALY-DE1156691745669174single base substitutionCTdownstream_gene_variant
MALY-DE1156692125669212single base substitutionCTdownstream_gene_variant
MELA-AU1156129815612981single base substitutionGAupstream_gene_variant
MELA-AU1156130325613032single base substitutionCTupstream_gene_variant
MELA-AU1156130935613093single base substitutionTGupstream_gene_variant
MELA-AU1156133605613360single base substitutionGAupstream_gene_variant
MELA-AU1156138565613856single base substitutionGAupstream_gene_variant
MELA-AU1156142225614222single base substitutionGAupstream_gene_variant
MELA-AU1156142505614250single base substitutionACupstream_gene_variant
MELA-AU1156142935614293single base substitutionGAupstream_gene_variant
MELA-AU1156146625614662single base substitutionGAupstream_gene_variant
MELA-AU1156146825614682single base substitutionTAupstream_gene_variant
MELA-AU1156148535614853single base substitutionTCupstream_gene_variant
MELA-AU1156150095615009single base substitutionCTupstream_gene_variant
MELA-AU1156154025615402single base substitutionCTupstream_gene_variant
MELA-AU1156154955615495single base substitutionGAupstream_gene_variant
MELA-AU1156155265615526single base substitutionCTupstream_gene_variant
MELA-AU1156156445615644single base substitutionCTupstream_gene_variant
MELA-AU1156157825615782single base substitutionCTupstream_gene_variant
MELA-AU1156157835615783single base substitutionCTupstream_gene_variant
MELA-AU1156160345616034single base substitutionGAupstream_gene_variant
MELA-AU1156161315616131single base substitutionCTupstream_gene_variant
MELA-AU1156161865616186single base substitutionGAupstream_gene_variant
MELA-AU1156163525616352single base substitutionTAupstream_gene_variant
MELA-AU1156163585616358single base substitutionCTupstream_gene_variant
MELA-AU1156163715616371single base substitutionCTupstream_gene_variant
MELA-AU1156166915616691single base substitutionCTupstream_gene_variant
MELA-AU1156172255617225single base substitutionCTupstream_gene_variant
MELA-AU1156173965617396single base substitutionACupstream_gene_variant
MELA-AU1156181185618118single base substitutionCT5_prime_UTR_variant
MELA-AU1156185715618571single base substitutionCTintron_variant
MELA-AU1156196665619666single base substitutionGAintron_variant
MELA-AU1156199685619968single base substitutionCTintron_variant
MELA-AU1156200895620089single base substitutionCTintron_variant
MELA-AU1156205355620535single base substitutionGAintron_variant
MELA-AU1156206645620664single base substitutionCTintron_variant
MELA-AU1156208665620866single base substitutionCTintron_variant
MELA-AU1156218675621867single base substitutionTGintron_variant
MELA-AU1156220855622085single base substitutionCTintron_variant
MELA-AU1156221785622178single base substitutionCTintron_variant
MELA-AU1156226745622674single base substitutionGAintron_variant
MELA-AU1156229565622956single base substitutionCTintron_variant
MELA-AU1156236665623666single base substitutionCTintron_variant
MELA-AU1156237355623735single base substitutionACintron_variant
MELA-AU1156237375623737single base substitutionCTintron_variant
MELA-AU1156238335623833single base substitutionGAintron_variant
MELA-AU1156239275623927single base substitutionTCintron_variant
MELA-AU1156242875624287single base substitutionTAintron_variant
MELA-AU1156244765624476single base substitutionGAsplice_region_variant
MELA-AU1156245705624570single base substitutionCTstop_gainedR38*112C>T
MELA-AU1156247475624747single base substitutionCTmissense_variantR97W289C>T
MELA-AU1156248725624873multiple base substitution (>=2bp and <=200bp)GGAAmissense_variantED138EN
MELA-AU1156252945625294single base substitutionCAintron_variant
MELA-AU1156262605626260single base substitutionGAintron_variant
MELA-AU1156264555626455single base substitutionCAintron_variant
MELA-AU1156265845626584single base substitutionGAsynonymous_variantE207E621G>A
MELA-AU1156267115626711single base substitutionGAmissense_variantD250N748G>A
MELA-AU1156268235626823single base substitutionCTintron_variant
MELA-AU1156273235627323single base substitutionCTintron_variant
MELA-AU1156277965627796single base substitutionTAintron_variant
MELA-AU1156279725627972single base substitutionCTintron_variant
MELA-AU1156289265628926single base substitutionCTintron_variant
MELA-AU1156292455629245single base substitutionGAintron_variant
MELA-AU1156298065629806single base substitutionGAintron_variant
MELA-AU1156304555630455single base substitutionGAintron_variant
MELA-AU1156305475630547single base substitutionATintron_variant
MELA-AU1156309225630922single base substitutionGAintron_variant
MELA-AU1156311075631107single base substitutionCTintron_variant
MELA-AU1156313025631302single base substitutionGAintron_variant
MELA-AU1156313585631358single base substitutionAGintron_variant
MELA-AU1156315535631553single base substitutionCTintron_variant
MELA-AU1156320835632084multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU1156323145632314single base substitutionGAintron_variant
MELA-AU1156324985632498single base substitutionCTintron_variant
MELA-AU1156331525633152single base substitutionTAintron_variant
MELA-AU1156333905633390single base substitutionCTintron_variant
MELA-AU1156341175634117single base substitutionCTintron_variant
MELA-AU1156341185634118single base substitutionCTintron_variant
MELA-AU1156354855635485single base substitutionTGintron_variant
MELA-AU1156354955635495single base substitutionCTintron_variant
MELA-AU1156360295636029single base substitutionTAintron_variant
MELA-AU1156362175636217single base substitutionCTintron_variant
MELA-AU1156367315636731single base substitutionATintron_variant
MELA-AU1156372045637204single base substitutionCTintron_variant
MELA-AU1156372125637212single base substitutionGAintron_variant
MELA-AU1156374175637417single base substitutionGCintron_variant
MELA-AU1156375135637513single base substitutionCTintron_variant
MELA-AU1156384215638421single base substitutionGAintron_variant
MELA-AU1156386525638652single base substitutionGAintron_variant
MELA-AU1156390545639054single base substitutionGAintron_variant
MELA-AU1156391145639114single base substitutionGAintron_variant
MELA-AU1156393105639310single base substitutionCTintron_variant
MELA-AU1156408505640850single base substitutionCTintron_variant
MELA-AU1156409015640902multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU1156410365641036single base substitutionGAintron_variant
MELA-AU1156410995641106deletion of <=200bpATTTTTGT-intron_variant
MELA-AU1156416085641608single base substitutionCTintron_variant
MELA-AU1156418065641807multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU1156422475642248multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU1156423515642351single base substitutionCTintron_variant
MELA-AU1156429855642985single base substitutionGAintron_variant
MELA-AU1156429895642989single base substitutionCTintron_variant
MELA-AU1156433845643384single base substitutionGAintron_variant
MELA-AU1156450425645042single base substitutionAGintron_variant
MELA-AU1156454315645431single base substitutionCTintron_variant
MELA-AU1156461075646108multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU1156461665646166single base substitutionCTintron_variant
MELA-AU1156462775646277single base substitutionCAintron_variant
MELA-AU1156463005646300single base substitutionGAintron_variant
MELA-AU1156464615646461single base substitutionTCintron_variant
MELA-AU1156466945646694single base substitutionTGintron_variant
MELA-AU1156477705647770single base substitutionGAintron_variant
MELA-AU1156490065649006single base substitutionCTintron_variant
MELA-AU1156490065649006single base substitutionCTupstream_gene_variant
MELA-AU1156491795649179single base substitutionTCintron_variant
MELA-AU1156491795649179single base substitutionTCupstream_gene_variant
MELA-AU1156493165649316single base substitutionGAintron_variant
MELA-AU1156493165649316single base substitutionGAupstream_gene_variant
MELA-AU1156495435649543single base substitutionCTintron_variant
MELA-AU1156495435649543single base substitutionCTupstream_gene_variant
MELA-AU1156496005649600single base substitutionCTintron_variant
MELA-AU1156496005649600single base substitutionCTupstream_gene_variant
MELA-AU1156496345649634single base substitutionCTintron_variant
MELA-AU1156496345649634single base substitutionCTupstream_gene_variant
MELA-AU1156496705649670single base substitutionCTintron_variant
MELA-AU1156496705649670single base substitutionCTupstream_gene_variant
MELA-AU1156498605649860single base substitutionGAintron_variant
MELA-AU1156498605649860single base substitutionGAupstream_gene_variant
MELA-AU1156504445650444single base substitutionTCintron_variant
MELA-AU1156504445650444single base substitutionTCupstream_gene_variant
MELA-AU1156505555650555single base substitutionCTintron_variant
MELA-AU1156505555650555single base substitutionCTupstream_gene_variant
MELA-AU1156506595650659single base substitutionCTintron_variant
MELA-AU1156506595650659single base substitutionCTupstream_gene_variant
MELA-AU1156507105650710single base substitutionCTintron_variant
MELA-AU1156507105650710single base substitutionCTupstream_gene_variant
MELA-AU1156509685650968single base substitutionCTintron_variant
MELA-AU1156509685650968single base substitutionCTupstream_gene_variant
MELA-AU1156510475651047single base substitutionCTintron_variant
MELA-AU1156510475651047single base substitutionCTupstream_gene_variant
MELA-AU1156511855651185single base substitutionCTintron_variant
MELA-AU1156511855651185single base substitutionCTupstream_gene_variant
MELA-AU1156512525651252single base substitutionCTintron_variant
MELA-AU1156512525651252single base substitutionCTupstream_gene_variant
MELA-AU1156517725651772single base substitutionCTintron_variant
MELA-AU1156517725651772single base substitutionCTupstream_gene_variant
MELA-AU1156522455652245single base substitutionCAintron_variant
MELA-AU1156522455652245single base substitutionCAupstream_gene_variant
MELA-AU1156524715652471single base substitutionCTintron_variant
MELA-AU1156524715652471single base substitutionCTupstream_gene_variant
MELA-AU1156525115652511single base substitutionCTintron_variant
MELA-AU1156525115652511single base substitutionCTupstream_gene_variant
MELA-AU1156526375652637single base substitutionACintron_variant
MELA-AU1156526375652637single base substitutionACupstream_gene_variant
MELA-AU1156535245653524single base substitutionCTmissense_variantS342L1025C>T
MELA-AU1156535245653524single base substitutionCTupstream_gene_variant
MELA-AU1156537165653716single base substitutionGAmissense_variantG406E1217G>A
MELA-AU1156537165653716single base substitutionGAmissense_variantG52E155G>A
MELA-AU1156542685654268single base substitutionCTintron_variant
MELA-AU1156544685654468single base substitutionCAintron_variant
MELA-AU1156546515654651single base substitutionCTintron_variant
MELA-AU1156546585654658single base substitutionCTintron_variant
MELA-AU1156550335655033single base substitutionGAsplice_acceptor_variant
MELA-AU1156551075655107single base substitutionGAmissense_variantR166K497G>A
MELA-AU1156551075655107single base substitutionGAmissense_variantR520K1559G>A
MELA-AU1156551225655122single base substitutionCTmissense_variantS171F512C>T
MELA-AU1156551225655122single base substitutionCTmissense_variantS525F1574C>T
MELA-AU1156554175655417single base substitutionGAintron_variant
MELA-AU1156554535655453single base substitutionCTintron_variant
MELA-AU1156554575655457single base substitutionTAintron_variant
MELA-AU1156554955655495single base substitutionGAintron_variant
MELA-AU1156556795655679single base substitutionCTintron_variant
MELA-AU1156561675656167single base substitutionGAintron_variant
MELA-AU1156565775656577single base substitutionCTintron_variant
MELA-AU1156568475656847single base substitutionGAintron_variant
MELA-AU1156569035656903single base substitutionCTintron_variant
MELA-AU1156570085657008single base substitutionCTintron_variant
MELA-AU1156572575657257single base substitutionTAintron_variant
MELA-AU1156574255657425single base substitutionGAintron_variant
MELA-AU1156575955657595single base substitutionGAintron_variant
MELA-AU1156576755657675single base substitutionCTintron_variant
MELA-AU1156578185657818single base substitutionCTintron_variant
MELA-AU1156581825658182single base substitutionCTintron_variant
MELA-AU1156582865658286single base substitutionCTintron_variant
MELA-AU1156583025658302single base substitutionCTintron_variant
MELA-AU1156584795658479single base substitutionCTintron_variant
MELA-AU1156585585658558single base substitutionGAintron_variant
MELA-AU1156588405658840single base substitutionGAintron_variant
MELA-AU1156589695658970multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU1156591715659171single base substitutionCGintron_variant
MELA-AU1156596345659634single base substitutionCTintron_variant
MELA-AU1156597965659796single base substitutionGAintron_variant
MELA-AU1156600955660095single base substitutionGTintron_variant
MELA-AU1156600965660096single base substitutionGAintron_variant
MELA-AU1156605915660591single base substitutionAGintron_variant
MELA-AU1156607035660703single base substitutionGAintron_variant
MELA-AU1156608645660864single base substitutionCTintron_variant
MELA-AU1156610605661060single base substitutionAGintron_variant
MELA-AU1156613345661334single base substitutionCTintron_variant
MELA-AU1156615465661546single base substitutionCTintron_variant
MELA-AU1156625825662583multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU1156626025662602single base substitutionGAintron_variant
MELA-AU1156626715662671single base substitutionCTintron_variant
MELA-AU1156631895663189single base substitutionCTintron_variant
MELA-AU1156633865663386single base substitutionCTintron_variant
MELA-AU1156634315663431single base substitutionCTintron_variant
MELA-AU1156636315663631single base substitutionCTsplice_region_variant
MELA-AU1156639565663956single base substitutionCTintron_variant
MELA-AU1156639855663985single base substitutionAGintron_variant
MELA-AU1156640615664061single base substitutionCTmissense_variantR297W889C>T
MELA-AU1156640615664061single base substitutionCTmissense_variantR651W1951C>T
MELA-AU1156641925664192single base substitutionTCintron_variant
MELA-AU1156642975664297single base substitutionAGintron_variant
MELA-AU1156651245665124single base substitutionCT3_prime_UTR_variant
MELA-AU1156651945665194single base substitutionCT3_prime_UTR_variant
MELA-AU1156652275665227single base substitutionGA3_prime_UTR_variant
MELA-AU1156654955665495single base substitutionCT3_prime_UTR_variant
MELA-AU1156659145665914single base substitutionCTdownstream_gene_variant
MELA-AU1156664475666447single base substitutionCTdownstream_gene_variant
MELA-AU1156670295667029single base substitutionCTdownstream_gene_variant
MELA-AU1156670565667056single base substitutionCTdownstream_gene_variant
MELA-AU1156678975667897single base substitutionCTdownstream_gene_variant
MELA-AU1156681925668192single base substitutionGAdownstream_gene_variant
MELA-AU1156686735668673single base substitutionGAdownstream_gene_variant
MELA-AU1156692825669282single base substitutionCTdownstream_gene_variant
MELA-AU1156694005669400single base substitutionCTdownstream_gene_variant
MELA-AU1156694665669466single base substitutionGAdownstream_gene_variant
MELA-AU1156697825669782single base substitutionCTdownstream_gene_variant
MELA-AU1156698155669815single base substitutionCTdownstream_gene_variant
MELA-AU1156699285669928single base substitutionGAdownstream_gene_variant
MELA-AU1156705515670551single base substitutionGAdownstream_gene_variant
ORCA-IN1156254075625407single base substitutionCTintron_variant
ORCA-IN1156368215636821single base substitutionGTintron_variant
ORCA-IN1156505065650506single base substitutionCGintron_variant
ORCA-IN1156505065650506single base substitutionCGupstream_gene_variant
ORCA-IN1156614715661471single base substitutionGAintron_variant
ORCA-IN1156655195665519single base substitutionGC3_prime_UTR_variant
ORCA-IN1156668235666823single base substitutionAGdownstream_gene_variant
OV-AU1156179765617976single base substitutionGT5_prime_UTR_premature_start_codon_gain_variant
OV-AU1156242305624230single base substitutionGAintron_variant
OV-AU1156296025629602single base substitutionGTmissense_variantD279Y835G>T
OV-AU1156298125629812single base substitutionGCintron_variant
OV-AU1156299465629946single base substitutionGAintron_variant
OV-AU1156312185631218single base substitutionCGintron_variant
OV-AU1156389445638944single base substitutionTGintron_variant
OV-AU1156392475639247single base substitutionCGintron_variant
OV-AU1156402695640269single base substitutionACintron_variant
OV-AU1156545065654506single base substitutionGAintron_variant
OV-AU1156552255655225single base substitutionGCintron_variant
OV-AU1156680675668067single base substitutionATdownstream_gene_variant
PACA-AU1156133515613351single base substitutionACupstream_gene_variant
PACA-AU1156140895614089single base substitutionGTupstream_gene_variant
PACA-AU1156151545615154single base substitutionTCupstream_gene_variant
PACA-AU1156153245615324single base substitutionTCupstream_gene_variant
PACA-AU1156201285620128single base substitutionGTintron_variant
PACA-AU1156209795620979single base substitutionTGintron_variant
PACA-AU1156251935625193single base substitutionGTintron_variant
PACA-AU1156273795627379single base substitutionGAintron_variant
PACA-AU1156292655629265single base substitutionAGintron_variant
PACA-AU1156321435632143single base substitutionCAintron_variant
PACA-AU1156481085648108single base substitutionGAintron_variant
PACA-AU1156510635651063single base substitutionGAintron_variant
PACA-AU1156510635651063single base substitutionGAupstream_gene_variant
PACA-AU1156535765653576single base substitutionCAsynonymous_variantI359I1077C>A
PACA-AU1156535765653576single base substitutionCAsynonymous_variantI5I15C>A
PACA-AU1156543835654383single base substitutionTCintron_variant
PACA-AU1156580825658082single base substitutionGAintron_variant
PACA-AU1156588475658847single base substitutionGTintron_variant
PACA-AU1156607375660737single base substitutionCTintron_variant
PACA-AU1156625845662584single base substitutionGAintron_variant
PACA-AU1156679625667962single base substitutionCGdownstream_gene_variant
PACA-CA1156146335614633insertion of <=200bp-Aupstream_gene_variant
PACA-CA1156152845615284single base substitutionCTupstream_gene_variant
PACA-CA1156232735623273single base substitutionCTintron_variant
PACA-CA1156263975626397single base substitutionAGintron_variant
PACA-CA1156273135627313single base substitutionGAintron_variant
PACA-CA1156280285628028single base substitutionCTintron_variant
PACA-CA1156281555628155single base substitutionCTintron_variant
PACA-CA1156298055629805single base substitutionGTintron_variant
PACA-CA1156317915631791single base substitutionGTmissense_variantA329S985G>T
PACA-CA1156356375635637single base substitutionGTintron_variant
PACA-CA1156368145636814single base substitutionTGintron_variant
PACA-CA1156371435637143single base substitutionTCintron_variant
PACA-CA1156434915643491single base substitutionTCintron_variant
PACA-CA1156476175647617single base substitutionTCintron_variant
PACA-CA1156487125648712single base substitutionGAintron_variant
PACA-CA1156487125648712single base substitutionGAupstream_gene_variant
PACA-CA1156491135649113single base substitutionTGintron_variant
PACA-CA1156491135649113single base substitutionTGupstream_gene_variant
PACA-CA1156520375652037single base substitutionAGintron_variant
PACA-CA1156520375652037single base substitutionAGupstream_gene_variant
PACA-CA1156522825652282single base substitutionGAintron_variant
PACA-CA1156522825652282single base substitutionGAupstream_gene_variant
PACA-CA1156557625655762single base substitutionTCintron_variant
PACA-CA1156563075656307single base substitutionTAintron_variant
PACA-CA1156591265659126single base substitutionGAintron_variant
PACA-CA1156642995664299single base substitutionCTintron_variant
PACA-CA1156654645665464single base substitutionAC3_prime_UTR_variant
PACA-CA1156679755667975single base substitutionAGdownstream_gene_variant
PAEN-AU1156255265625526single base substitutionGTintron_variant
PAEN-AU1156267275626727single base substitutionCTmissense_variantT255I764C>T
PAEN-AU1156319015631901single base substitutionGAintron_variant
PAEN-AU1156698605669860single base substitutionATdownstream_gene_variant
PAEN-IT1156593795659379single base substitutionTCintron_variant
PBCA-DE1156251985625198single base substitutionGAintron_variant
PBCA-DE1156390775639077insertion of <=200bp-Aintron_variant
PBCA-DE1156404975640497single base substitutionTCintron_variant
PBCA-DE1156478525647852single base substitutionGTintron_variant
PBCA-DE1156488305648830single base substitutionAGintron_variant
PBCA-DE1156488305648830single base substitutionAGupstream_gene_variant
PBCA-DE1156505095650509insertion of <=200bp-AAAACintron_variant
PBCA-DE1156505095650509insertion of <=200bp-AAAACupstream_gene_variant
PBCA-DE1156582715658271single base substitutionCTintron_variant
PBCA-DE1156614955661495single base substitutionGAintron_variant
PBCA-DE1156626895662689single base substitutionGAintron_variant
PRAD-CA1156305415630541single base substitutionTCintron_variant
PRAD-CA1156600365660036single base substitutionCAintron_variant
PRAD-CA1156671105667110single base substitutionATdownstream_gene_variant
PRAD-CA1156671375667137single base substitutionACdownstream_gene_variant
PRAD-UK1156147175614717single base substitutionGAupstream_gene_variant
PRAD-UK1156158605615860single base substitutionTCupstream_gene_variant
PRAD-UK1156222265622226single base substitutionCGintron_variant
PRAD-UK1156309535630953single base substitutionCAintron_variant
PRAD-UK1156396535639653single base substitutionTGintron_variant
PRAD-UK1156457165645716single base substitutionGTintron_variant
PRAD-UK1156611745661174single base substitutionCGintron_variant
PRAD-UK1156672245667224insertion of <=200bp-TATAATTATATATTTATAAATTATATATAATTTATATATATATATATAAATTATAdownstream_gene_variant
PRAD-US1156324245632424single base substitutionAGintron_variant
PRAD-US1156325565632556single base substitutionGAintron_variant
READ-US1156249525624952single base substitutionCTmissense_variantA165V494C>T
READ-US1156267625626762single base substitutionCTmissense_variantR267C799C>T
RECA-EU1156368155636815single base substitutionTGintron_variant
RECA-EU1156476065647606single base substitutionCTintron_variant
RECA-EU1156482775648277single base substitutionCAintron_variant
RECA-EU1156686805668680single base substitutionAGdownstream_gene_variant
SKCA-BR1156131255613125single base substitutionCAupstream_gene_variant
SKCA-BR1156141615614161single base substitutionGAupstream_gene_variant
SKCA-BR1156141685614168single base substitutionGAupstream_gene_variant
SKCA-BR1156160675616067single base substitutionTGupstream_gene_variant
SKCA-BR1156173165617316single base substitutionCTupstream_gene_variant
SKCA-BR1156196965619696single base substitutionAGintron_variant
SKCA-BR1156232785623278single base substitutionTCintron_variant
SKCA-BR1156234855623485single base substitutionATintron_variant
SKCA-BR1156237485623748single base substitutionGCintron_variant
SKCA-BR1156242415624241single base substitutionCTintron_variant
SKCA-BR1156255645625564single base substitutionGAintron_variant
SKCA-BR1156260455626045single base substitutionCTintron_variant
SKCA-BR1156260685626068single base substitutionCTintron_variant
SKCA-BR1156270545627054single base substitutionTAintron_variant
SKCA-BR1156279685627968single base substitutionGAintron_variant
SKCA-BR1156280725628072single base substitutionGAintron_variant
SKCA-BR1156287345628734single base substitutionTGintron_variant
SKCA-BR1156293255629325single base substitutionAGintron_variant
SKCA-BR1156300655630065single base substitutionCTintron_variant
SKCA-BR1156348315634831single base substitutionGAintron_variant
SKCA-BR1156363995636399single base substitutionGCintron_variant
SKCA-BR1156371655637165single base substitutionTCintron_variant
SKCA-BR1156373065637306single base substitutionGCintron_variant
SKCA-BR1156380505638050single base substitutionAGintron_variant
SKCA-BR1156387165638717deletion of <=200bpCT-intron_variant
SKCA-BR1156390035639003single base substitutionGAintron_variant
SKCA-BR1156390115639011single base substitutionCTintron_variant
SKCA-BR1156407785640778single base substitutionTGintron_variant
SKCA-BR1156407835640783single base substitutionCGintron_variant
SKCA-BR1156407895640789single base substitutionCGintron_variant
SKCA-BR1156410065641006single base substitutionCTintron_variant
SKCA-BR1156413965641396insertion of <=200bp-TAintron_variant
SKCA-BR1156441835644183single base substitutionGAintron_variant
SKCA-BR1156443575644357single base substitutionATintron_variant
SKCA-BR1156477265647726single base substitutionGAintron_variant
SKCA-BR1156477275647727single base substitutionGAintron_variant
SKCA-BR1156481435648143single base substitutionGCintron_variant
SKCA-BR1156542235654225deletion of <=200bpATT-intron_variant
SKCA-BR1156549815654981single base substitutionCTintron_variant
SKCA-BR1156551505655150single base substitutionTAintron_variant
SKCA-BR1156579505657950single base substitutionCTintron_variant
SKCA-BR1156604975660497single base substitutionATintron_variant
SKCA-BR1156623085662308single base substitutionCTintron_variant
SKCA-BR1156643565664356insertion of <=200bp-TATATAGAintron_variant
SKCA-BR1156643565664356insertion of <=200bp-TATATATAintron_variant
SKCA-BR1156648295664829single base substitutionGAmissense_variantG453S1357G>A
SKCA-BR1156648295664829single base substitutionGAmissense_variantG807S2419G>A
SKCA-BR1156653735665373single base substitutionCT3_prime_UTR_variant
SKCA-BR1156670975667097insertion of <=200bp-GAAdownstream_gene_variant
SKCA-BR1156671095667109single base substitutionATdownstream_gene_variant
SKCA-BR1156700195670019single base substitutionTCdownstream_gene_variant
SKCM-US1156247435624743single base substitutionCGmissense_variantN95K285C>G
SKCM-US1156248605624860single base substitutionCTsynonymous_variantL134L402C>T
SKCM-US1156258355625835single base substitutionCTsynonymous_variantI193I579C>T
SKCM-US1156265845626584single base substitutionGAsynonymous_variantE207E621G>A
SKCM-US1156266725626672single base substitutionGAmissense_variantE237K709G>A
SKCM-US1156267115626711single base substitutionGAmissense_variantD250N748G>A
SKCM-US1156267435626743single base substitutionGAsynonymous_variantE260E780G>A
SKCM-US1156267655626765single base substitutionCTstop_gainedR268*802C>T
SKCM-US1156317895631789single base substitutionGAstop_gainedW328*983G>A
SKCM-US1156321035632103single base substitutionCTintron_variant
SKCM-US1156323145632314single base substitutionGAintron_variant
SKCM-US1156323845632384single base substitutionACintron_variant
SKCM-US1156538725653872single base substitutionTGmissense_variantL104R311T>G
SKCM-US1156538725653872single base substitutionTGmissense_variantL458R1373T>G
SKCM-US1156550335655033single base substitutionGAsplice_acceptor_variant
SKCM-US1156550665655066single base substitutionGAsynonymous_variantK152K456G>A
SKCM-US1156550665655066single base substitutionGAsynonymous_variantK506K1518G>A
SKCM-US1156551145655114single base substitutionGAsynonymous_variantE168E504G>A
SKCM-US1156551145655114single base substitutionGAsynonymous_variantE522E1566G>A
SKCM-US1156640615664061single base substitutionCTmissense_variantR297W889C>T
SKCM-US1156640615664061single base substitutionCTmissense_variantR651W1951C>T
SKCM-US1156643875664387single base substitutionGAsynonymous_variantL305L915G>A
SKCM-US1156643875664387single base substitutionGAsynonymous_variantL659L1977G>A
SKCM-US1156644225664422single base substitutionCTmissense_variantS317L950C>T
SKCM-US1156644225664422single base substitutionCTmissense_variantS671L2012C>T
SKCM-US1156645315664531single base substitutionGAsynonymous_variantV353V1059G>A
SKCM-US1156645315664531single base substitutionGAsynonymous_variantV707V2121G>A
SKCM-US1156645845664584single base substitutionCTmissense_variantS371F1112C>T
SKCM-US1156645845664584single base substitutionCTmissense_variantS725F2174C>T
SKCM-US1156647135664713single base substitutionCTmissense_variantS414F1241C>T
SKCM-US1156647135664713single base substitutionCTmissense_variantS768F2303C>T
SKCM-US1156648135664813single base substitutionCTsynonymous_variantF447F1341C>T
SKCM-US1156648135664813single base substitutionCTsynonymous_variantF801F2403C>T
STAD-US1156247425624742single base substitutionACmissense_variantN95T284A>C
STAD-US1156247485624748single base substitutionGAmissense_variantR97Q290G>A
STAD-US1156248615624861single base substitutionTCmissense_variantF135L403T>C
STAD-US1156249315624931single base substitutionCTmissense_variantT158M473C>T
STAD-US1156249395624939single base substitutionGAmissense_variantV161M481G>A
STAD-US1156257925625792single base substitutionTGmissense_variantL179R536T>G
STAD-US1156313845631384single base substitutionCAmissense_variantF289L867C>A
STAD-US1156322785632278single base substitutionTGintron_variant
STAD-US1156325565632556single base substitutionGAintron_variant
STAD-US1156536075653607insertion of <=200bp-Cframeshift_variantP16P?
STAD-US1156536075653607insertion of <=200bp-Cframeshift_variantP370P?
STAD-US1156539095653909single base substitutionCAstop_gainedC116*348C>A
STAD-US1156539095653909single base substitutionCAstop_gainedC470*1410C>A
STAD-US1156559845655984single base substitutionAGmissense_variantK215E643A>G
STAD-US1156559845655984single base substitutionAGmissense_variantK569E1705A>G
STAD-US1156560435656043single base substitutionCTsynonymous_variantI234I702C>T
STAD-US1156560435656043single base substitutionCTsynonymous_variantI588I1764C>T
THCA-SA1156325015632501single base substitutionACintron_variant
THCA-US1156247805624780single base substitutionCTmissense_variantR108W322C>T
THCA-US1156535655653565single base substitutionGCmissense_variantA2P4G>C
THCA-US1156535655653565single base substitutionGCmissense_variantA356P1066G>C
UCEC-US1156257995625799single base substitutionCTsynonymous_variantN181N543C>T
UCEC-US1156266915626691single base substitutionTAmissense_variantI243N728T>A
UCEC-US1156267395626739single base substitutionGAmissense_variantR259Q776G>A
UCEC-US1156267625626762single base substitutionCTmissense_variantR267C799C>T
UCEC-US1156267745626774single base substitutionGAmissense_variantG271R811G>A
UCEC-US1156313625631362single base substitutionCAintron_variant
UCEC-US1156323965632396single base substitutionCTintron_variant
UCEC-US1156323975632397single base substitutionGAintron_variant
UCEC-US1156537615653761single base substitutionAGmissense_variantH421R1262A>G
UCEC-US1156537615653761single base substitutionAGmissense_variantH67R200A>G
UCEC-US1156559035655903single base substitutionGTmissense_variantD188Y562G>T
UCEC-US1156559035655903single base substitutionGTmissense_variantD542Y1624G>T
UCEC-US1156559745655974single base substitutionGTmissense_variantK211N633G>T
UCEC-US1156559745655974single base substitutionGTmissense_variantK565N1695G>T
UCEC-US1156559765655976single base substitutionCTmissense_variantT212M635C>T
UCEC-US1156559765655976single base substitutionCTmissense_variantT566M1697C>T
UCEC-US1156624295662429single base substitutionGAintron_variant
UCEC-US1156624575662457single base substitutionTCintron_variant
UCEC-US1156636785663678single base substitutionGTmissense_variantK272N816G>T
UCEC-US1156636785663678single base substitutionGTmissense_variantK626N1878G>T
UCEC-US1156646315664631single base substitutionCAmissense_variantL387I1159C>A
UCEC-US1156646315664631single base substitutionCAmissense_variantL741I2221C>A
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-AY-6196-01COSM1354699c.1187G>Tp.G396VSubstitution - Missense11:5643429-5643429+
TCGA-34-5239-01COSM688452c.2459A>Tp.Q820LSubstitution - Missense11:5643639-5643639+
TCGA-BS-A0UF-01COSM928483c.200A>Gp.H67RSubstitution - Missense11:5632531-5632531+
TCGA-AA-A00N-01COSM277806c.749A>Gp.D250GSubstitution - Missense11:5605482-5605482+
7285COSM5613400c.892C>Ap.L298ISubstitution - Missense11:5610179-5610179+
tumor_4107137COSM5947168c.1965G>Ap.V655VSubstitution - coding silent11:5643145-5643145+
8057482COSM3383588c.15C>Ap.I5ISubstitution - coding silent11:5632346-5632346+
CHEWS030COSM4574475c.1759C>Tp.L587FSubstitution - Missense11:5634808-5634808+
TCGA-AX-A05Z-01COSM928487c.633G>Tp.K211NSubstitution - Missense11:5634744-5634744+
LUAD-YINHDCOSM348459c.2314G>Cp.D772HSubstitution - Missense11:5643494-5643494+
PT08_1COSM5893614c.870G>Ap.W290*Substitution - Nonsense11:5610157-5610157+
CSCC-55-TCOSM4481093c.1421C>Tp.P474LSubstitution - Missense11:5643663-5643663+
2492726COSM5724916c.284A>Tp.N95ISubstitution - Missense11:5603512-5603512+
Pat_58_BCOSM4033920c.473C>Tp.T158MSubstitution - Missense11:5603701-5603701+
T578COSM4736186c.504G>Tp.E168DSubstitution - Missense11:5633884-5633884+
YUMERCOSM1703471c.1630C>Tp.L544FSubstitution - Missense11:5634679-5634679+
SNUH_G73_S1COSM3998473c.528A>Gp.L176LSubstitution - coding silent11:5604554-5604554+
TCGA-B5-A0JY-01COSM928491c.773+10G>Ap.?Unknown11:5641199-5641199+
PT14_1COSM5897035c.423+4G>Ap.?Unknown11:5632758-5632758+
CHC1035TCOSM3666939c.258G>Ap.V86VSubstitution - coding silent11:5603486-5603486+
10-P083COSM4574466c.281_284delGGAAp.G94fs*11Deletion - Frameshift11:5603509-5603512+
CSCC-38-TCOSM3449586c.1112C>Tp.S371FSubstitution - Missense11:5643354-5643354+
TCGA-AY-6196-01COSM1354698c.2249G>Tp.G750VSubstitution - Missense11:5643429-5643429+
TCGA-43-5668-01COSM688517c.827T>Ap.L276QSubstitution - Missense11:5605560-5605560+
TCGA-CG-5721-01COSM4033924c.536T>Gp.L179RSubstitution - Missense11:5604562-5604562+
LUAD-RT-S01832COSM384590c.255T>Ap.P85PSubstitution - coding silent11:5603483-5603483+
CRC-1COSM304232c.11A>Cp.K4TSubstitution - Missense11:5632342-5632342+
TCGA-ER-A3PL-06COSM3869525c.2303C>Tp.S768FSubstitution - Missense11:5643483-5643483+
TARGET-20-PAPXRJ-04A-02DCOSM5487690c.975A>Gp.Q325QSubstitution - coding silent11:5610551-5610551+
TCGA-09-2050-01COSM73064c.1240G>Cp.G414RSubstitution - Missense11:5632509-5632509+
SNUH_G76_S1COSM147124c.844G>Cp.D282HSubstitution - Missense11:5642476-5642476+
CSCC-20-TCOSM4529395c.546G>Tp.R182SSubstitution - Missense11:5634657-5634657+
pfg125TCOSM4749199c.567G>Tp.Q189HSubstitution - Missense11:5634678-5634678+
TCGA-AP-A056-01COSM928402c.776G>Ap.R259QSubstitution - Missense11:5605509-5605509+
pfg181TCOSM4749201c.2125G>Ap.V709MSubstitution - Missense11:5643305-5643305+
TCGA-CD-8536-01COSM4033922c.481G>Ap.V161MSubstitution - Missense11:5603709-5603709+
TCGA-DD-A113-01COSM4925309c.1872T>Cp.V624VSubstitution - coding silent11:5642442-5642442+
TCGA-BJ-A0Z0-01COSM3368427c.1066G>Cp.A356PSubstitution - Missense11:5632335-5632335+
TCGA-EE-A17X-06COSM3449459c.579C>Tp.I193ISubstitution - coding silent11:5604605-5604605+
TCGA-CZ-4862-01COSM3773604c.86A>Tp.D29VSubstitution - Missense11:5632417-5632417+
PD24212aCOSM5802580c.894_901+7>CTGAAAp.?Unknown11:5642836-5642850+
CHC432TCOSM4953952c.398C>Tp.T133MSubstitution - Missense11:5632729-5632729+
TCGA-EE-A181-06COSM3449575c.1373T>Gp.L458RSubstitution - Missense11:5632642-5632642+
Pat_32_BCOSM5838808c.863A>Gp.Q288RSubstitution - Missense11:5642495-5642495+
Pat_32_BCOSM5838807c.1925A>Gp.Q642RSubstitution - Missense11:5642495-5642495+
CSCC-38-TCOSM3449585c.2174C>Tp.S725FSubstitution - Missense11:5643354-5643354+
TCGA-C5-A1BQ-01COSM4842347c.1627C>Ap.Q543KSubstitution - Missense11:5634676-5634676+
TCGA-D8-A147-01COSM429240c.273C>Gp.Y91*Substitution - Nonsense11:5603501-5603501+
TCGA-B5-A0JY-01COSM928493c.1159C>Ap.L387ISubstitution - Missense11:5643401-5643401+
TCGA-HU-8243-01COSM4033976c.1410C>Ap.C470*Substitution - Nonsense11:5632679-5632679+
10-104COSM3736595c.1361C>Tp.S454FSubstitution - Missense11:5643603-5643603+
T3503COSM4736182c.376C>Tp.R126CSubstitution - Missense11:5632707-5632707+
PTC-28CCOSM4145901c.1488G>Cp.E496DSubstitution - Missense11:5633806-5633806+
sysucc-882TCOSM5446922c.1583A>Gp.Y528CSubstitution - Missense11:5634632-5634632+
TCGA-FW-A3R5-06COSM3869522c.915G>Ap.L305LSubstitution - coding silent11:5643157-5643157+
WA7COSM242049c.358G>Cp.E120QSubstitution - Missense11:5632689-5632689+
CHEWS030COSM4574476c.697C>Tp.L233FSubstitution - Missense11:5634808-5634808+
CSCC-62-TCOSM4481252c.2494C>Tp.P832SSubstitution - Missense11:5643674-5643674+
TCGA-AX-A05Z-01COSM928485c.562G>Tp.D188YSubstitution - Missense11:5634673-5634673+
TCGA-AM-5821-01COSM3752489c.2421C>Ap.G807GSubstitution - coding silent11:5643601-5643601+
TCGA-AM-5820-01COSM3752488c.1212T>Gp.N404KSubstitution - Missense11:5643454-5643454+
TCGA-BT-A20T-01COSM415554c.1071G>Cp.K357NSubstitution - Missense11:5643313-5643313+
TCGA-AP-A051-01COSM285951c.799C>Tp.R267CSubstitution - Missense11:5605532-5605532+
PCSI_0504_Pa_P_526COSM4806672c.985G>Tp.A329SSubstitution - Missense11:5610561-5610561+
TCGA-BR-4361-01COSM4033916c.290G>Ap.R97QSubstitution - Missense11:5603518-5603518+
T3203COSM4736188c.719G>Ap.R240QSubstitution - Missense11:5634830-5634830+
ESCC-D15COSM5045524c.2303C>Gp.S768CSubstitution - Missense11:5643483-5643483+
PT44COSM5926811c.1068C>Tp.S356SSubstitution - coding silent11:5643310-5643310+
TCGA-BS-A0UF-01COSM928482c.1262A>Gp.H421RSubstitution - Missense11:5632531-5632531+
TCGA-EE-A3J5-06COSM3449587c.2403C>Tp.F801FSubstitution - coding silent11:5643583-5643583+
CSCC-20-TCOSM4456874c.1025C>Tp.S342LSubstitution - Missense11:5632294-5632294+
TCGA-CZ-4862-01COSM3773603c.1148A>Tp.D383VSubstitution - Missense11:5632417-5632417+
CHC432TCOSM4953951c.1460C>Tp.T487MSubstitution - Missense11:5632729-5632729+
WA7COSM242048c.1420G>Cp.E474QSubstitution - Missense11:5632689-5632689+
I2L-P19Tb-Tumor-BiopsyCOSM179228c.655C>Tp.R219*Substitution - Nonsense11:5605388-5605388+
TCGA-BJ-A0Z0-01COSM3368428c.4G>Cp.A2PSubstitution - Missense11:5632335-5632335+
TCGA-HU-A4G8-01COSM4033920c.473C>Tp.T158MSubstitution - Missense11:5603701-5603701+
LIM1899COSM4639754c.1835+4C>Tp.?Unknown11:5641193-5641193+
TCGA-CM-5861-01COSM1354681c.207G>Ap.Q69QSubstitution - coding silent11:5632538-5632538+
TCGA-BT-A20T-01COSM415553c.2133G>Cp.K711NSubstitution - Missense11:5643313-5643313+
PT20_2COSM5900779c.956G>Ap.R319KSubstitution - Missense11:5610243-5610243+
TCGA-EA-A439-01COSM4843704c.519+1G>Tp.?Unknown11:5633900-5633900+
TCGA-AX-A05Z-01COSM928486c.1695G>Tp.K565NSubstitution - Missense11:5634744-5634744+
3N44-VS-3T44COSM4982162c.453G>Ap.L151LSubstitution - coding silent11:5633833-5633833+
CHC432TCOSM4953951c.1460C>Tp.T487MSubstitution - Missense11:5632729-5632729+
TCGA-EE-A29D-06COSM3449580c.504G>Ap.E168ESubstitution - coding silent11:5633884-5633884+
TCGA-CG-4437-01COSM4033981c.702C>Tp.I234ISubstitution - coding silent11:5634813-5634813+
BD114TCOSM4639755c.773+4C>Tp.?Unknown11:5641193-5641193+
TCGA-HU-8243-01COSM4033977c.348C>Ap.C116*Substitution - Nonsense11:5632679-5632679+
TCGA-BR-7958-01COSM4033914c.284A>Cp.N95TSubstitution - Missense11:5603512-5603512+
TCGA-EE-A29L-06COSM3449577c.1486-1G>Ap.?Unknown11:5633803-5633803+
TCGA-IN-7806-01COSM4033979c.643A>Gp.K215ESubstitution - Missense11:5634754-5634754+
WA16COSM242046c.725G>Ap.R242QSubstitution - Missense11:5605458-5605458+
Pat_32_ACOSM5838808c.863A>Gp.Q288RSubstitution - Missense11:5642495-5642495+
MedB-1COSM5622047c.938A>Gp.N313SSubstitution - Missense11:5643180-5643180+
PTC-28CCOSM4145902c.426G>Cp.E142DSubstitution - Missense11:5633806-5633806+
TCGA-B0-5083-01COSM1492581c.706G>Cp.E236QSubstitution - Missense11:5605439-5605439+
TCGA-56-6546-01COSM688455c.775A>Gp.S259GSubstitution - Missense11:5642407-5642407+
SNUH_G76_S1COSM147123c.1906G>Cp.D636HSubstitution - Missense11:5642476-5642476+
BD189TCOSM5508380c.2216A>Gp.Q739RSubstitution - Missense11:5643396-5643396+
CSCC-55-TCOSM4481092c.2483C>Tp.P828LSubstitution - Missense11:5643663-5643663+
TCGA-D3-A2JP-06COSM3449584c.950C>Tp.S317LSubstitution - Missense11:5643192-5643192+
S02209COSM5675089c.1182A>Gp.L394LSubstitution - coding silent11:5643424-5643424+
TCGA-AX-A05Z-01COSM928484c.1624G>Tp.D542YSubstitution - Missense11:5634673-5634673+
BD114TCOSM4639754c.1835+4C>Tp.?Unknown11:5641193-5641193+
SM-4AX85COSM5035060c.1740G>Ap.Q580QSubstitution - coding silent11:5634789-5634789+
pfg064TCOSM4749189c.539A>Cp.K180TSubstitution - Missense11:5604565-5604565+
TCGA-AR-A254-01COSM1475546c.914T>Ap.M305KSubstitution - Missense11:5610201-5610201+
GC8_TCOSM147124c.844G>Cp.D282HSubstitution - Missense11:5642476-5642476+
TCGA-FW-A3R5-06COSM3869520c.456G>Ap.K152KSubstitution - coding silent11:5633836-5633836+
TCGA-CK-5916-01COSM5154362c.508-2_508delAGGp.?Unknown11:5604532-5604534+
CSCC-41-TCOSM4469242c.158C>Tp.P53LSubstitution - Missense11:5603386-5603386+
CHC1594TCOSM4805017c.391A>Cp.K131QSubstitution - Missense11:5603619-5603619+
TCGA-AP-A056-01COSM928489c.635C>Tp.T212MSubstitution - Missense11:5634746-5634746+
TCGA-CC-A7IK-01COSM4924684c.313A>Gp.I105VSubstitution - Missense11:5603541-5603541+
sysucc-274TCOSM5475534c.959-5T>Cp.?Unknown11:5610530-5610530+
TCGA-AA-A010-01COSM285953c.1047C>Tp.S349SSubstitution - coding silent11:5632316-5632316+
2492724COSM5724916c.284A>Tp.N95ISubstitution - Missense11:5603512-5603512+
TCGA-CM-4743-01COSM1354679c.195T>Cp.F65FSubstitution - coding silent11:5632526-5632526+
T263COSM4736190c.1319A>Gp.E440GSubstitution - Missense11:5643561-5643561+
TCGA-P5-A5F1-01COSM3967616c.74G>Ap.R25KSubstitution - Missense11:5603302-5603302+
T3225COSM4736183c.1455C>Tp.V485VSubstitution - coding silent11:5632724-5632724+
TCGA-AZ-4615-01COSM5139633c.710_712delAGAp.K239delKDeletion - In frame11:5605443-5605445+
TCGA-FS-A1ZZ-06COSM3449469c.709G>Ap.E237KSubstitution - Missense11:5605442-5605442+
LIM1899COSM4639755c.773+4C>Tp.?Unknown11:5641193-5641193+
GHE0988COSM5714940c.507G>Ap.Q169QSubstitution - coding silent11:5603735-5603735+
TCGA-AO-A0J3-01COSM429230c.39C>Gp.I13MSubstitution - Missense11:5603267-5603267+
pfg181TCOSM4749202c.1063G>Ap.V355MSubstitution - Missense11:5643305-5643305+
TCGA-DD-A113-01COSM4925310c.810T>Cp.V270VSubstitution - coding silent11:5642442-5642442+
TCGA-D3-A2JP-06COSM3449583c.2012C>Tp.S671LSubstitution - Missense11:5643192-5643192+
ESCC_11COSM5624184c.1463C>Gp.S488CSubstitution - Missense11:5643705-5643705+
TCGA-AP-A0LM-01COSM179242c.816G>Tp.K272NSubstitution - Missense11:5642448-5642448+
TCGA-FW-A3R5-06COSM3869494c.780G>Ap.E260ESubstitution - coding silent11:5605513-5605513+
HCC128TCOSM5824426c.808C>Tp.Q270*Substitution - Nonsense11:5605541-5605541+
TCGA-FW-A3R5-06COSM3869524c.1059G>Ap.V353VSubstitution - coding silent11:5643301-5643301+
BD124TCOSM928389c.543C>Tp.N181NSubstitution - coding silent11:5604569-5604569+
TCGA-CM-6674-01COSM1354697c.793delAp.K266fs*9Deletion - Frameshift11:5642425-5642425+
TCGA-12-3649-01COSM3397850c.889G>Ap.A297TSubstitution - Missense11:5610176-5610176+
ESCC_71COSM3449587c.2403C>Tp.F801FSubstitution - coding silent11:5643583-5643583+
LUAD-YINHDCOSM348460c.1252G>Cp.D418HSubstitution - Missense11:5643494-5643494+
TCGA-56-6546-01COSM688454c.1837A>Gp.S613GSubstitution - Missense11:5642407-5642407+
PD4601aCOSM165146c.1364G>Cp.G455ASubstitution - Missense11:5632633-5632633+
TCGA-EE-A3AA-06COSM3449467c.621G>Ap.E207ESubstitution - coding silent11:5605354-5605354+
TCGA-09-2050-01COSM73065c.178G>Cp.G60RSubstitution - Missense11:5632509-5632509+
CRC-19TCOSM5480885c.800G>Ap.R267HSubstitution - Missense11:5605533-5605533+
B89-12COSM1746325c.207A>Cp.P69PSubstitution - coding silent11:5603435-5603435+
PD4601aCOSM165147c.302G>Cp.G101ASubstitution - Missense11:5632633-5632633+
3N44-VS-3T44COSM4982161c.1515G>Ap.L505LSubstitution - coding silent11:5633833-5633833+
TCGA-AA-A010-01COSM285954c.1383C>Ap.F461LSubstitution - Missense11:5632652-5632652+
PT08_2COSM5893614c.870G>Ap.W290*Substitution - Nonsense11:5610157-5610157+
HCC31TCOSM1604744c.123G>Tp.V41VSubstitution - coding silent11:5603351-5603351+
B105-TumorCOSM147124c.844G>Cp.D282HSubstitution - Missense11:5642476-5642476+
BD189TCOSM5508381c.1154A>Gp.Q385RSubstitution - Missense11:5643396-5643396+
T3444COSM4736178c.164G>Tp.S55ISubstitution - Missense11:5603392-5603392+
TCGA-B5-A0JY-01COSM285951c.799C>Tp.R267CSubstitution - Missense11:5605532-5605532+
T3225COSM4736184c.393C>Tp.V131VSubstitution - coding silent11:5632724-5632724+
TCGA-B5-A0JY-01COSM928490c.1835+10G>Ap.?Unknown11:5641199-5641199+
YUMERCOSM1703472c.568C>Tp.L190FSubstitution - Missense11:5634679-5634679+
TCGA-CJ-5676-01COSM466978c.519G>Cp.K173NSubstitution - Missense11:5633899-5633899+
TCGA-CM-4743-01COSM1354678c.1257T>Cp.F419FSubstitution - coding silent11:5632526-5632526+
TCGA-AD-6964-01COSM285953c.1047C>Tp.S349SSubstitution - coding silent11:5632316-5632316+
PT44COSM5926810c.2130C>Tp.S710SSubstitution - coding silent11:5643310-5643310+
TCGA-EI-6882-01COSM285951c.799C>Tp.R267CSubstitution - Missense11:5605532-5605532+
S02209COSM5675088c.2244A>Gp.L748LSubstitution - coding silent11:5643424-5643424+
AOCS-075-1-0COSM3980417c.835G>Tp.D279YSubstitution - Missense11:5608372-5608372+
49MCOSM5593588c.683G>Ap.R228QSubstitution - Missense11:5605416-5605416+
MedB-1COSM5622046c.2000A>Gp.N667SSubstitution - Missense11:5643180-5643180+
ESCC_71COSM3449588c.1341C>Tp.F447FSubstitution - coding silent11:5643583-5643583+
CRC-1COSM304231c.1073A>Cp.K358TSubstitution - Missense11:5632342-5632342+
TCGA-CA-6718-01COSM1354695c.765C>Ap.I255ISubstitution - coding silent11:5641181-5641181+
TCGA-FW-A3R5-06COSM3869521c.1977G>Ap.L659LSubstitution - coding silent11:5643157-5643157+
587284COSM1230376c.1450A>Gp.T484ASubstitution - Missense11:5632719-5632719+
TCGA-IN-7806-01COSM4033978c.1705A>Gp.K569ESubstitution - Missense11:5634754-5634754+
LUAD-RT-S01774COSM381315c.449C>Tp.S150FSubstitution - Missense11:5603677-5603677+
ESCC_92COSM5637023c.412G>Ap.E138KSubstitution - Missense11:5603640-5603640+
TCGA-F5-6814-01COSM3415983c.494C>Tp.A165VSubstitution - Missense11:5603722-5603722+
TCGA-EE-A3J5-06COSM3449588c.1341C>Tp.F447FSubstitution - coding silent11:5643583-5643583+
SC_9058COSM5557755c.564G>Cp.K188NSubstitution - Missense11:5604590-5604590+
TCGA-EE-A20C-06COSM3449581c.1951C>Tp.R651WSubstitution - Missense11:5642831-5642831+
CSCC-17-TCOSM4523029c.132G>Ap.K44KSubstitution - coding silent11:5632463-5632463+
TCGA-AP-A0LM-01COSM179241c.1878G>Tp.K626NSubstitution - Missense11:5642448-5642448+
HCT-15COSM1675779c.169G>Tp.D57YSubstitution - Missense11:5603397-5603397+
HCC31COSM1604744c.123G>Tp.V41VSubstitution - coding silent11:5603351-5603351+
TCGA-AP-A056-01COSM928488c.1697C>Tp.T566MSubstitution - Missense11:5634746-5634746+
Pat_32_ACOSM5838807c.1925A>Gp.Q642RSubstitution - Missense11:5642495-5642495+
TCGA-FS-A1ZK-06COSM3449498c.983G>Ap.W328*Substitution - Nonsense11:5610559-5610559+
T263COSM4736189c.2381A>Gp.E794GSubstitution - Missense11:5643561-5643561+
TCGA-FS-A1ZZ-06COSM3449586c.1112C>Tp.S371FSubstitution - Missense11:5643354-5643354+
2492725COSM5724916c.284A>Tp.N95ISubstitution - Missense11:5603512-5603512+
10-104COSM3736594c.2423C>Tp.S808FSubstitution - Missense11:5643603-5643603+
TCGA-FS-A1ZZ-06COSM3449585c.2174C>Tp.S725FSubstitution - Missense11:5643354-5643354+
T578COSM4736185c.1566G>Tp.E522DSubstitution - Missense11:5633884-5633884+
CSCC-17-TCOSM4523028c.1194G>Ap.K398KSubstitution - coding silent11:5632463-5632463+
TCGA-EE-A29L-06COSM3449578c.424-1G>Ap.?Unknown11:5633803-5633803+
TCGA-EB-A3XD-01COSM3449454c.402C>Tp.L134LSubstitution - coding silent11:5603630-5603630+
TCGA-CG-4437-01COSM4033980c.1764C>Tp.I588ISubstitution - coding silent11:5634813-5634813+
TCGA-C5-A1BQ-01COSM4842348c.565C>Ap.Q189KSubstitution - Missense11:5634676-5634676+
pfg073TCOSM4749196c.1549G>Cp.A517PSubstitution - Missense11:5633867-5633867+
CSCC-62-TCOSM4481253c.1432C>Tp.P478SSubstitution - Missense11:5643674-5643674+
TCGA-AA-A010-01COSM285951c.799C>Tp.R267CSubstitution - Missense11:5605532-5605532+
TCGA-ER-A3PL-06COSM3869526c.1241C>Tp.S414FSubstitution - Missense11:5643483-5643483+
8057482COSM3383587c.1077C>Ap.I359ISubstitution - coding silent11:5632346-5632346+
GC8_TCOSM147123c.1906G>Cp.D636HSubstitution - Missense11:5642476-5642476+
TCGA-BR-8080-01COSM4033918c.403T>Cp.F135LSubstitution - Missense11:5603631-5603631+
TCGA-B5-A0JY-01COSM928492c.2221C>Ap.L741ISubstitution - Missense11:5643401-5643401+
TCGA-34-5239-01COSM688453c.1397A>Tp.Q466LSubstitution - Missense11:5643639-5643639+
PT49COSM5935811c.1294G>Ap.V432MSubstitution - Missense11:5632563-5632563+
TCGA-A8-A0A6-01COSM3809539c.758A>Cp.H253PSubstitution - Missense11:5605491-5605491+
SWE-48COSM1180140c.1058G>Ap.S353NSubstitution - Missense11:5632327-5632327+
CHC1594TCOSM4805017c.391A>Cp.K131QSubstitution - Missense11:5603619-5603619+
ZZUFHECRKL-G026TCOSM5435611c.770C>Tp.S257LSubstitution - Missense11:5605503-5605503+
TCGA-DK-A1AC-01COSM1298184c.18G>Ap.R6RSubstitution - coding silent11:5603246-5603246+
I2L-P19Tb-Tumor-OrganoidCOSM179228c.655C>Tp.R219*Substitution - Nonsense11:5605388-5605388+
TCGA-GN-A26C-01COSM3449471c.802C>Tp.R268*Substitution - Nonsense11:5605535-5605535+
T3203COSM4736187c.1781G>Ap.R594QSubstitution - Missense11:5634830-5634830+
TCGA-AM-5821-01COSM3752490c.1359C>Ap.G453GSubstitution - coding silent11:5643601-5643601+
J90_TCOSM3953389c.135C>Ap.I45ISubstitution - coding silent11:5603363-5603363+
tumor_4107137COSM5947169c.903G>Ap.V301VSubstitution - coding silent11:5643145-5643145+
CHC1035TCOSM3666939c.258G>Ap.V86VSubstitution - coding silent11:5603486-5603486+
TCGA-C8-A12K-01COSM429232c.149T>Ap.L50QSubstitution - Missense11:5603377-5603377+
TCGA-12-3649-01COSM3397844c.682C>Tp.R228WSubstitution - Missense11:5605415-5605415+
TCGA-28-5209-01COSM3747883c.593C>Ap.T198KSubstitution - Missense11:5604619-5604619+
BRC29COSM5027350c.996G>Tp.G332GSubstitution - coding silent11:5632265-5632265+
TCGA-26-1442-01COSM3397864c.1758G>Tp.E586DSubstitution - Missense11:5634807-5634807+
PT49COSM5935812c.232G>Ap.V78MSubstitution - Missense11:5632563-5632563+
PD4956aCOSM543119c.446G>Ap.R149QSubstitution - Missense11:5603674-5603674+
TCGA-AA-A010-01COSM285955c.321C>Ap.F107LSubstitution - Missense11:5632652-5632652+
Pat_60_ACOSM5838810c.1150C>Tp.R384CSubstitution - Missense11:5643392-5643392+
PD24212aCOSM5802579c.1956_1963+7>CTGAAAp.?Unknown11:5642836-5642850+
ESCC-D15COSM5045525c.1241C>Gp.S414CSubstitution - Missense11:5643483-5643483+
TCGA-EE-A181-06COSM3449576c.311T>Gp.L104RSubstitution - Missense11:5632642-5632642+
TCGA-DK-A1AC-01COSM1298186c.402C>Gp.L134LSubstitution - coding silent11:5603630-5603630+
HCC067TCOSM5824025c.605T>Ap.L202QSubstitution - Missense11:5634716-5634716+
pfg038TCOSM4749191c.722T>Gp.L241RSubstitution - Missense11:5605455-5605455+
B105-TumorCOSM147123c.1906G>Cp.D636HSubstitution - Missense11:5642476-5642476+
sysucc-882TCOSM5446923c.521A>Gp.Y174CSubstitution - Missense11:5634632-5634632+
T3503COSM4736181c.1438C>Tp.R480CSubstitution - Missense11:5632707-5632707+
YUFITCOSM5372794c.1010G>Ap.R337KSubstitution - Missense11:5632279-5632279+
T3147COSM4736181c.1438C>Tp.R480CSubstitution - Missense11:5632707-5632707+
CSCC-20-TCOSM4529394c.1608G>Tp.R536SSubstitution - Missense11:5634657-5634657+
SM-4AX85COSM5035061c.678G>Ap.Q226QSubstitution - coding silent11:5634789-5634789+
TCGA-CA-6717-01COSM179228c.655C>Tp.R219*Substitution - Nonsense11:5605388-5605388+
HCC067TCOSM5824024c.1667T>Ap.L556QSubstitution - Missense11:5634716-5634716+
TCGA-EA-A439-01COSM4843703c.1581+1G>Tp.?Unknown11:5633900-5633900+
19685COSM5346200c.590A>Cp.K197TSubstitution - Missense11:5604616-5604616+
587284COSM1230377c.388A>Gp.T130ASubstitution - Missense11:5632719-5632719+
SNUH_G10_S1COSM3998473c.528A>Gp.L176LSubstitution - coding silent11:5604554-5604554+
TCGA-AA-A010-01COSM299567c.603+9G>Ap.?Unknown11:5604638-5604638+
pfg125TCOSM4749198c.1629G>Tp.Q543HSubstitution - Missense11:5634678-5634678+
CHC432TCOSM4953952c.398C>Tp.T133MSubstitution - Missense11:5632729-5632729+
GC8_TCOSM147121c.840G>Ap.V280VSubstitution - coding silent11:5608377-5608377+
TCGA-EL-A4K4-01COSM3368424c.322C>Tp.R108WSubstitution - Missense11:5603550-5603550+
pfg073TCOSM4749197c.487G>Cp.A163PSubstitution - Missense11:5633867-5633867+
TCGA-AA-A01Z-01COSM300450c.1045C>Tp.H349YSubstitution - Missense11:5643287-5643287+
Pat_60_ACOSM5838809c.2212C>Tp.R738CSubstitution - Missense11:5643392-5643392+
TCGA-EE-A2A2-06COSM3449452c.285C>Gp.N95KSubstitution - Missense11:5603513-5603513+
TCGA-FW-A3R5-06COSM3869523c.2121G>Ap.V707VSubstitution - coding silent11:5643301-5643301+
T3090COSM4736191c.2522G>Ap.S841NSubstitution - Missense11:5643702-5643702+
SC_9008COSM5558529c.395T>Cp.L132PSubstitution - Missense11:5603623-5603623+
TCGA-BH-A18G-01COSM3809560c.106C>Tp.R36*Substitution - Nonsense11:5632437-5632437+
TCGA-AA-A01Z-01COSM300449c.2107C>Tp.H703YSubstitution - Missense11:5643287-5643287+
TCGA-CM-5861-01COSM1354680c.1269G>Ap.Q423QSubstitution - coding silent11:5632538-5632538+
TCGA-CM-6674-01COSM1354696c.1855delAp.K620fs*9Deletion - Frameshift11:5642425-5642425+
T3147COSM4736182c.376C>Tp.R126CSubstitution - Missense11:5632707-5632707+
PT14_1COSM5897034c.1485+4G>Ap.?Unknown11:5632758-5632758+
TCGA-AM-5820-01COSM3752487c.2274T>Gp.N758KSubstitution - Missense11:5643454-5643454+
TCGA-EE-A20C-06COSM3449582c.889C>Tp.R297WSubstitution - Missense11:5642831-5642831+
TCGA-BR-8680-01COSM4033941c.867C>Ap.F289LSubstitution - Missense11:5610154-5610154+
B89-12-TumorCOSM1746325c.207A>Cp.P69PSubstitution - coding silent11:5603435-5603435+
587222COSM1230374c.388G>Tp.E130*Substitution - Nonsense11:5603616-5603616+
TCGA-FW-A3R5-06COSM3869519c.1518G>Ap.K506KSubstitution - coding silent11:5633836-5633836+
TCGA-EE-A29D-06COSM3449579c.1566G>Ap.E522ESubstitution - coding silent11:5633884-5633884+
ESCC_11COSM5624183c.2525C>Gp.S842CSubstitution - Missense11:5643705-5643705+
TCGA-BH-A18G-01COSM3809559c.1168C>Tp.R390*Substitution - Nonsense11:5632437-5632437+
TCGA-CA-6718-01COSM1354694c.1827C>Ap.I609ISubstitution - coding silent11:5641181-5641181+
T3090COSM4736192c.1460G>Ap.S487NSubstitution - Missense11:5643702-5643702+
TCGA-BS-A0UJ-01COSM928404c.811G>Ap.G271RSubstitution - Missense11:5605544-5605544+
631056COSM326759c.564G>Tp.K188NSubstitution - Missense11:5604590-5604590+
TCGA-AP-A059-01COSM928389c.543C>Tp.N181NSubstitution - coding silent11:5604569-5604569+
8051710COSM4135685c.764C>Tp.T255ISubstitution - Missense11:5605497-5605497+
TCGA-FW-A3R5-06COSM3869492c.748G>Ap.D250NSubstitution - Missense11:5605481-5605481+
TCGA-26-1442-01COSM3397865c.696G>Tp.E232DSubstitution - Missense11:5634807-5634807+
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGMissensep.S259Gc.775A>G115663637LUSC
ATMissensep.D29Vc.86A>T115653647RCCC
ATMissensep.Q466Lc.1397A>T115664869LUSC
ATSpliceAcceptorSNV.c.424-2A>T115655032LUAD
CCTTMissensep.S425Fc.1274_1275delinsTT115664746CM
CTMissensep.A295Vc.884C>T115664056CM
CTMissensep.H349Yc.1045C>T115664517COREAD
CTMissensep.R297Wc.889C>T115664061CM
CTMissensep.S317Lc.950C>T115664422CM
CTMissensep.S371Fc.1112C>T115664584CM
GAMissensep.A46Tc.136G>A115653697LUAD
GAMissensep.E207Kc.619G>A115655960CM
GAMissensep.G52Ec.155G>A115653716CM
GASpliceAcceptorSNV.c.424-1G>A115655033CM
GCMissensep.A2Pc.4G>C115653565THCA
GCMissensep.G101Ac.302G>C115653863BRCA
GCMissensep.G60Rc.178G>C115653739OV
GCMissensep.K173Nc.519G>C115655129RCCC
GCMissensep.K357Nc.1071G>C115664543BLCA
GTMissensep.E232Dc.696G>T115656037GBM
GTNonsensep.E110*c.328G>T115653889HNSC
TGMissensep.L104Rc.311T>G115653872CM
AC-Frameshiftp.D57Vfs*42c.170_171delAC115624628BRCA
AGMissensep.K231Ec.691A>G115626654CM
AGMissensep.S613Gc.1837A>G115663637LUSC
ATMissensep.D383Vc.1148A>T115653647RCCC
ATMissensep.Q820Lc.2459A>T115664869LUSC
ATMissensep.Q9Lc.26A>T115624484HNSC
ATSpliceAcceptorSNV.c.1486-2A>T115655032LUAD
CAMissensep.L298Ic.892C>A115631409NSCLC
CAMissensep.T198Kc.593C>A115625849GBM
CCTTMissensep.S779Fc.2336_2337delinsTT115664746CM
CGMissensep.I13Mc.39C>G115624497BRCA
CGMissensep.N95Kc.285C>G115624743CM
CGNonsensep.Y91*c.273C>G115624731BRCA
CTMissensep.A649Vc.1946C>T115664056CM
CTMissensep.H703Yc.2107C>T115664517COREAD
CTMissensep.R228Wc.682C>T115626645GBM
CTMissensep.R651Wc.1951C>T115664061CM
CTMissensep.S671Lc.2012C>T115664422CM
CTMissensep.S725Fc.2174C>T115664584CM
CTNonsensep.Q88*c.262C>T115624720STAD
CTNonsensep.R268*c.802C>T115626765CM
GAMissensep.A297Tc.889G>A115631406GBM
GAMissensep.A400Tc.1198G>A115653697LUAD
GAMissensep.E237Kc.709G>A115626672CM
GAMissensep.E561Kc.1681G>A115655960CM
GAMissensep.G406Ec.1217G>A115653716CM
GAMissensep.R149Qc.446G>A115624904LUAD
GANonsensep.W328*c.983G>A115631789CM
GASpliceAcceptorSNV.c.1486-1G>A115655033CM
GCMissensep.A356Pc.1066G>C115653565THCA
GCMissensep.G414Rc.1240G>C115653739OV
GCMissensep.G455Ac.1364G>C115653863BRCA
GCMissensep.K527Nc.1581G>C115655129RCCC
GCMissensep.K711Nc.2133G>C115664543BLCA
GGA-InFrameDeletionp.E163delEc.488_490delAGG115624941RCCC
GTMissensep.E586Dc.1758G>T115656037GBM
GTMissensep.K188Nc.564G>T115625820SCLC
GTNonsensep.E464*c.1390G>T115653889HNSC
GTSpliceAcceptorSNV.c.18-1G>T115624475STAD
TAMissensep.I243Nc.728T>A115626691UCEC
TAMissensep.L276Qc.827T>A115626790LUSC
TAMissensep.L50Qc.149T>A115624607BRCA
TAMissensep.M305Kc.914T>A115631431BRCA
TGMissensep.F159Vc.475T>G115624933RCCC
TGMissensep.L458Rc.1373T>G115653872CM