KAT6A
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
ACC84179051341790513+Missense_MutationSNPCCTTCGA-OR-A5KB-01A-11D-A30A-10TCGA-OR-A5KB-11A-11D-A30A-10g.chr8:41790513C>Tc.5225G>Ac.(5224-5226)gGc>gAcp.G1742D
ACC84179101741791017+Missense_MutationSNPCCTTCGA-OR-A5K9-01A-11D-A29I-10TCGA-OR-A5K9-11A-11D-A29L-10g.chr8:41791017C>Tc.4721G>Ac.(4720-4722)gGc>gAcp.G1574D
ACC84179848441798484+Missense_MutationSNPCCTTCGA-OR-A5JI-01A-11D-A29I-10TCGA-OR-A5JI-10A-01D-A29L-10g.chr8:41798484C>Tc.2915G>Ac.(2914-2916)cGc>cAcp.R972H
BLCA84178995041789950+Missense_MutationSNPGGATCGA-DK-A6B5-01A-11D-A31L-08TCGA-DK-A6B5-10A-01D-A31J-08g.chr8:41789950G>Ac.5788C>Tc.(5788-5790)Ccc>Tccp.P1930S
BLCA84179051741790517+Missense_MutationSNPCCATCGA-CU-A3YL-01A-11D-A22Z-08TCGA-CU-A3YL-10A-01D-A22Z-08g.chr8:41790517C>Ac.5221G>Tc.(5221-5223)Gcc>Tccp.A1741S
BLCA84179065941790659+SilentSNPTTGTCGA-E7-A677-01A-11D-A30E-08TCGA-E7-A677-10A-01D-A30H-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
BLCA84179068241790682+Missense_MutationSNPGGCTCGA-XF-A9SM-01A-11D-A42E-08TCGA-XF-A9SM-10A-01D-A42H-08g.chr8:41790682G>Cc.5056C>Gc.(5056-5058)Cag>Gagp.Q1686E
BLCA84179087241790872+Missense_MutationSNPGGCTCGA-UY-A9PD-01A-11D-A38G-08TCGA-UY-A9PD-10A-01D-A38J-08g.chr8:41790872G>Cc.4866C>Gc.(4864-4866)agC>agGp.S1622R
BLCA84179111141791111+Missense_MutationSNPGGCTCGA-XF-AAML-01A-11D-A42E-08TCGA-XF-AAML-10A-01D-A42H-08g.chr8:41791111G>Cc.4627C>Gc.(4627-4629)Cag>Gagp.Q1543E
BLCA84179131541791315+Missense_MutationSNPGGATCGA-4Z-AA7R-01A-11D-A391-08TCGA-4Z-AA7R-10A-01D-A394-08g.chr8:41791315G>Ac.4423C>Tc.(4423-4425)Cat>Tatp.H1475Y
BLCA84179139941791399+Missense_MutationSNPCCTTCGA-XF-AAN2-01A-11D-A42E-08TCGA-XF-AAN2-10A-01D-A42H-08g.chr8:41791399C>Tc.4339G>Ac.(4339-4341)Gag>Aagp.E1447K
BLCA84179152541791525+Missense_MutationSNPCCTTCGA-DK-A2I6-01A-12D-A18F-08TCGA-DK-A2I6-10A-01D-A18F-08g.chr8:41791525C>Tc.4213G>Ac.(4213-4215)Gag>Aagp.E1405K
BLCA84179235941792359+Missense_MutationSNPGGCTCGA-E5-A2PC-01A-11D-A202-08TCGA-E5-A2PC-10B-01D-A202-08g.chr8:41792359G>Cc.3379C>Gc.(3379-3381)Ctt>Gttp.L1127V
BLCA84179488241794882+Missense_MutationSNPTTCTCGA-CU-A0YR-01A-12D-A10S-08TCGA-CU-A0YR-10A-01D-A10S-08g.chr8:41794882T>Cc.3244A>Gc.(3244-3246)Aga>Ggap.R1082G
BLCA84179854641798546+SilentSNPGGCTCGA-XF-A9SY-01A-21D-A42E-08TCGA-XF-A9SY-10A-01D-A42H-08g.chr8:41798546G>Cc.2853C>Gc.(2851-2853)ctC>ctGp.L951L
BLCA84179873841798738+SilentSNPGGATCGA-DK-A6B6-01A-11D-A30E-08TCGA-DK-A6B6-10A-01D-A30H-08g.chr8:41798738G>Ac.2661C>Tc.(2659-2661)ctC>ctTp.L887L
BLCA84180046641800466+Nonsense_MutationSNPGGATCGA-ZF-AA51-01A-21D-A391-08TCGA-ZF-AA51-10A-01D-A394-08g.chr8:41800466G>Ac.2281C>Tc.(2281-2283)Cag>Tagp.Q761*
BLCA84180132141801321+Missense_MutationSNPGGCTCGA-E7-A7DV-01A-11D-A339-08TCGA-E7-A7DV-10A-01D-A339-08g.chr8:41801321G>Cc.2173C>Gc.(2173-2175)Caa>Gaap.Q725E
BLCA84183230541832305+Missense_MutationSNPCCTTCGA-XF-A9SY-01A-21D-A42E-08TCGA-XF-A9SY-10A-01D-A42H-08g.chr8:41832305C>Tc.1399G>Ac.(1399-1401)Gag>Aagp.E467K
BLCA84190606641906066+Missense_MutationSNPGGCTCGA-XF-A9SM-01A-11D-A42E-08TCGA-XF-A9SM-10A-01D-A42H-08g.chr8:41906066G>Cc.430C>Gc.(430-432)Cac>Gacp.H144D
BLCA84190617941906179+Missense_MutationSNPGGATCGA-DK-AA74-01A-11D-A391-08TCGA-DK-AA74-10A-01D-A394-08g.chr8:41906179G>Ac.317C>Tc.(316-318)gCa>gTap.A106V
BLCA84190629541906295+Frame_Shift_DelDELTT-TCGA-E7-A7XN-01A-11D-A34U-08TCGA-E7-A7XN-10A-01D-A34X-08g.chr8:41906295delTc.201delAc.(199-201)ggafsp.G67fs
BLCA84190630541906305+Nonsense_MutationSNPGGCTCGA-FD-A3SS-01A-12D-A22Z-08TCGA-FD-A3SS-10A-01D-A22Z-08g.chr8:41906305G>Cc.191C>Gc.(190-192)tCa>tGap.S64*
BLCA84190638341906383+Missense_MutationSNPGGATCGA-E7-A5KF-01A-11D-A289-08TCGA-E7-A5KF-10A-01D-A289-08g.chr8:41906383G>Ac.113C>Tc.(112-114)tCa>tTap.S38L
BRCA84179060541790605+SilentSNPGGATCGA-C8-A27B-01A-11D-A167-09TCGA-C8-A27B-10A-01D-A167-09g.chr8:41790605G>Ac.5133C>Tc.(5131-5133)ttC>ttTp.F1711F
BRCA84179065341790653+SilentSNPAAGTCGA-D8-A3Z5-01A-41D-A243-09TCGA-D8-A3Z5-10A-01D-A243-09g.chr8:41790653A>Gc.5085T>Cc.(5083-5085)ccT>ccCp.P1695P
BRCA84179065941790659+SilentSNPTTGTCGA-D8-A3Z5-01A-41D-A243-09TCGA-D8-A3Z5-10A-01D-A243-09g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
BRCA84179183041791830+Missense_MutationSNPTTCTCGA-C8-A275-01A-21D-A16D-09TCGA-C8-A275-10A-01D-A16D-09g.chr8:41791830T>Cc.3908A>Gc.(3907-3909)gAt>gGtp.D1303G
BRCA84179187141791873+In_Frame_DelDELCTCCTC-TCGA-BH-A18G-01A-11D-A12B-09TCGA-BH-A18G-10A-01D-A12B-09g.chr8:41791871_41791873delCTCc.3865_3867delGAGc.(3865-3867)gagdelp.E1289del
BRCA84179198041791980+Missense_MutationSNPGGATCGA-BH-A0B6-01A-11D-A19Y-09TCGA-BH-A0B6-10A-01D-A19Y-09g.chr8:41791980G>Ac.3758C>Tc.(3757-3759)tCt>tTtp.S1253F
BRCA84179223241792232+Missense_MutationSNPCCTTCGA-A8-A093-01A-11W-A019-09TCGA-A8-A093-10A-01W-A021-09g.chr8:41792232C>Tc.3506G>Ac.(3505-3507)cGa>cAap.R1169Q
BRCA84179838641798386+Missense_MutationSNPGGTTCGA-AN-A046-01A-21W-A050-09TCGA-AN-A046-10A-01W-A055-09g.chr8:41798386G>Tc.3013C>Ac.(3013-3015)Ctc>Atcp.L1005I
BRCA84179858841798588+Missense_MutationSNPCCGTCGA-BH-A18P-01A-11D-A12B-09TCGA-BH-A18P-11A-43D-A12B-09g.chr8:41798588C>Gc.2811G>Cc.(2809-2811)aaG>aaCp.K937N
BRCA84183458841834588+Missense_MutationSNPGGCTCGA-AC-A23H-01A-11D-A159-09TCGA-AC-A23H-11A-12D-A17G-09g.chr8:41834588G>Cc.1301C>Gc.(1300-1302)tCt>tGtp.S434C
BRCA84190616241906162+Missense_MutationSNPCCGTCGA-D8-A1JA-01A-11D-A13L-09TCGA-D8-A1JA-10A-01W-A14R-09g.chr8:41906162C>Gc.334G>Cc.(334-336)Gag>Cagp.E112Q
CESC84178976641789766+Missense_MutationSNPCCTTCGA-EA-A3HT-01A-61D-A21Q-09TCGA-EA-A3HT-10A-01D-A21Q-09g.chr8:41789766C>Tc.5972G>Ac.(5971-5973)gGc>gAcp.G1991D
CESC84179074941790749+SilentSNPCCTTCGA-EA-A3HU-01A-11D-A20U-09TCGA-EA-A3HU-10B-01D-A20U-09g.chr8:41790749C>Tc.4989G>Ac.(4987-4989)ccG>ccAp.P1663P
CESC84179840741798407+Missense_MutationSNPGGATCGA-MU-A51Y-01A-11D-A26G-09TCGA-MU-A51Y-10A-01D-A26G-09g.chr8:41798407G>Ac.2992C>Tc.(2992-2994)Cgg>Tggp.R998W
CESC84179892241798922+Missense_MutationSNPGGCTCGA-JW-A5VI-01A-11D-A28B-09TCGA-JW-A5VI-10A-01D-A28E-09g.chr8:41798922G>Cc.2477C>Gc.(2476-2478)tCt>tGtp.S826C
CESC84190638641906386+Missense_MutationSNPGGTTCGA-C5-A1BK-01B-11D-A13W-08TCGA-C5-A1BK-10A-01D-A13W-08g.chr8:41906386G>Tc.110C>Ac.(109-111)tCt>tAtp.S37Y
CHOL84180687741806877+Missense_MutationSNPGGTTCGA-W5-AA2G-01A-11D-A417-09TCGA-W5-AA2G-10A-01D-A41A-09g.chr8:41806877G>Tc.1603C>Ac.(1603-1605)Ccc>Accp.P535T
COAD84178977341789773+Missense_MutationSNPCCTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr8:41789773C>Tc.5965G>Ac.(5965-5967)Gct>Actp.A1989T
COAD84179001641790016+Missense_MutationSNPCCTTCGA-AA-A00A-01A-01W-A005-10TCGA-AA-A00A-10A-01W-A005-10g.chr8:41790016C>Tc.5722G>Ac.(5722-5724)Gcc>Accp.A1908T
COAD84179005441790054+Missense_MutationSNPCCTTCGA-AD-6889-01A-11D-1924-10TCGA-AD-6889-10A-01D-1924-10g.chr8:41790054C>Tc.5684G>Ac.(5683-5685)cGt>cAtp.R1895H
COAD84179007041790070+Missense_MutationSNPCCTTCGA-AZ-4682-01B-01D-1408-10TCGA-AZ-4682-10A-01D-1408-10g.chr8:41790070C>Tc.5668G>Ac.(5668-5670)Gca>Acap.A1890T
COAD84179049341790493+Missense_MutationSNPCCTTCGA-G4-6625-01A-21D-1771-10TCGA-G4-6625-11A-01D-1771-10g.chr8:41790493C>Tc.5245G>Ac.(5245-5247)Gcc>Accp.A1749T
COAD84179065941790660+Frame_Shift_InsINS--GTCGA-AZ-6598-01A-11D-1771-10TCGA-AZ-6598-11A-01D-1771-10g.chr8:41790659_41790660insGc.5078_5079insCc.(5077-5079)ccafsp.P1693fs
COAD84179067441790674+SilentSNPCCTTCGA-AA-3715-01A-01W-0900-09TCGA-AA-3715-10A-01W-0900-09g.chr8:41790674C>Tc.5064G>Ac.(5062-5064)caG>caAp.Q1688Q
COAD84179125141791251+Missense_MutationSNPGGATCGA-AA-A00N-01A-02W-A00E-09TCGA-AA-A00N-10A-01W-A00E-09g.chr8:41791251G>Ac.4487C>Tc.(4486-4488)tCg>tTgp.S1496L
COAD84179131141791311+Missense_MutationSNPGGATCGA-AA-A00A-01A-01W-A005-10TCGA-AA-A00A-10A-01W-A005-10g.chr8:41791311G>Ac.4427C>Tc.(4426-4428)gCg>gTgp.A1476V
COAD84179201141792011+Frame_Shift_DelDELCC-TCGA-CM-4743-01A-01D-1719-10TCGA-CM-4743-10A-01D-1719-10g.chr8:41792011delCc.3727delGc.(3727-3729)gatfsp.D1243fs
COAD84179214541792145+Missense_MutationSNPGGATCGA-AA-3989-01A-01W-0995-10TCGA-AA-3989-10A-01W-0999-10g.chr8:41792145G>Ac.3593C>Tc.(3592-3594)gCt>gTtp.A1198V
COAD84179492541794925+SilentSNPGGATCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr8:41794925G>Ac.3201C>Tc.(3199-3201)atC>atTp.I1067I
COAD84179846941798469+Missense_MutationSNPTTCTCGA-AA-3525-01A-02W-0833-10TCGA-AA-3525-10A-01W-0833-10g.chr8:41798469T>Cc.2930A>Gc.(2929-2931)gAc>gGcp.D977G
COAD84179848441798484+Missense_MutationSNPCCTTCGA-AA-A00N-01A-02W-A00E-09TCGA-AA-A00N-10A-01W-A00E-09g.chr8:41798484C>Tc.2915G>Ac.(2914-2916)cGc>cAcp.R972H
COAD84179848741798487+Missense_MutationSNPCCTTCGA-CM-6171-01A-11D-1650-10TCGA-CM-6171-10A-01D-1650-10g.chr8:41798487C>Tc.2912G>Ac.(2911-2913)cGt>cAtp.R971H
COAD84179849541798495+SilentSNPCCTTCGA-D5-6930-01A-11D-1924-10TCGA-D5-6930-10A-01D-1924-10g.chr8:41798495C>Tc.2904G>Ac.(2902-2904)agG>agAp.R968R
COAD84179880841798808+Missense_MutationSNPCCTTCGA-AA-3710-01A-01W-0995-10TCGA-AA-3710-10A-01W-0995-10g.chr8:41798808C>Tc.2591G>Ac.(2590-2592)cGg>cAgp.R864Q
COAD84179894741798947+Missense_MutationSNPAAGTCGA-AA-A01Q-01A-01W-A005-10TCGA-AA-A01Q-10A-01W-A005-10g.chr8:41798947A>Gc.2452T>Cc.(2452-2454)Tct>Cctp.S818P
COAD84180147541801475+Missense_MutationSNPTTATCGA-AA-3663-01A-01D-1719-10TCGA-AA-3663-11A-01D-1719-10g.chr8:41801475T>Ac.2019A>Tc.(2017-2019)gaA>gaTp.E673D
COAD84180147541801475+SilentSNPTTCTCGA-AU-3779-01A-01D-1719-10TCGA-AU-3779-10A-01D-1719-10g.chr8:41801475T>Cc.2019A>Gc.(2017-2019)gaA>gaGp.E673E
COAD84180147741801477+Nonsense_MutationSNPCCATCGA-A6-5661-01A-01D-1650-10TCGA-A6-5661-10A-01D-1650-10g.chr8:41801477C>Ac.2017G>Tc.(2017-2019)Gaa>Taap.E673*
COAD84180411541804115+Missense_MutationSNPCCTTCGA-AA-A00N-01A-02W-A00E-09TCGA-AA-A00N-10A-01W-A00E-09g.chr8:41804115C>Tc.1990G>Ac.(1990-1992)Gat>Aatp.D664N
COAD84180411541804115+Missense_MutationSNPCCTTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr8:41804115C>Tc.1990G>Ac.(1990-1992)Gat>Aatp.D664N
COAD84180541741805417+Missense_MutationSNPAAGTCGA-A6-5665-01A-01D-1650-10TCGA-A6-5665-10A-01D-1650-10g.chr8:41805417A>Gc.1754T>Cc.(1753-1755)gTg>gCgp.V585A
COAD84180541741805417+Missense_MutationSNPAAGTCGA-G4-6303-01A-11D-1771-10TCGA-G4-6303-10A-01D-1771-10g.chr8:41805417A>Gc.1754T>Cc.(1753-1755)gTg>gCgp.V585A
COAD84181283741812837+SilentSNPGGATCGA-AD-5900-01A-11D-1650-10TCGA-AD-5900-10A-01D-1650-10g.chr8:41812837G>Ac.1575C>Tc.(1573-1575)tcC>tcTp.S525S
COAD84181284041812840+SilentSNPGGATCGA-F4-6807-01A-11D-1835-10TCGA-F4-6807-10A-01D-1835-10g.chr8:41812840G>Ac.1572C>Tc.(1570-1572)tcC>tcTp.S524S
COAD84183233641832336+SilentSNPAAGTCGA-DM-A28K-01A-21D-A16V-10TCGA-DM-A28K-10A-01D-A16V-10g.chr8:41832336A>Gc.1368T>Cc.(1366-1368)aaT>aaCp.N456N
COAD84183233741832337+Missense_MutationSNPTTCTCGA-AZ-6607-01A-11D-1835-10TCGA-AZ-6607-11A-01D-1835-10g.chr8:41832337T>Cc.1367A>Gc.(1366-1368)aAt>aGtp.N456S
COAD84183233741832337+Missense_MutationSNPTTCTCGA-DM-A28E-01A-11D-A16V-10TCGA-DM-A28E-10A-01D-A16V-10g.chr8:41832337T>Cc.1367A>Gc.(1366-1368)aAt>aGtp.N456S
COAD84183233741832337+Missense_MutationSNPTTCTCGA-G4-6315-01A-11D-1719-10TCGA-G4-6315-10A-01D-1720-10g.chr8:41832337T>Cc.1367A>Gc.(1366-1368)aAt>aGtp.N456S
COAD84183457641834576+Missense_MutationSNPCCTTCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr8:41834576C>Tc.1313G>Ac.(1312-1314)cGa>cAap.R438Q
COAD84183616241836162+SilentSNPCCTTCGA-CM-4746-01A-01D-1408-10TCGA-CM-4746-10A-01D-1408-10g.chr8:41836162C>Tc.1041G>Ac.(1039-1041)acG>acAp.T347T
COAD84183621541836215+Missense_MutationSNPGGATCGA-AA-3949-01A-01W-0995-10TCGA-AA-3949-10A-01W-0995-10g.chr8:41836215G>Ac.988C>Tc.(988-990)Cgc>Tgcp.R330C
COAD84190626041906260+Missense_MutationSNPCCTTCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr8:41906260C>Tc.236G>Ac.(235-237)cGa>cAap.R79Q
COAD84190636541906365+Missense_MutationSNPCCTTCGA-AA-3525-01A-02W-0833-10TCGA-AA-3525-10A-01W-0833-10g.chr8:41906365C>Tc.131G>Ac.(130-132)cGt>cAtp.R44H
COADREAD84178977341789773+Missense_MutationSNPCCTTCGA-AA-A010-01A-01W-A00E-09TCGA-AA-A010-10A-01W-A00E-09g.chr8:41789773C>Tc.5965G>Ac.(5965-5967)Gct>Actp.A1989T
COADREAD84179001641790016+Missense_MutationSNPCCTTCGA-AA-A00A-01A-01W-A005-10TCGA-AA-A00A-10A-01W-A005-10g.chr8:41790016C>Tc.5722G>Ac.(5722-5724)Gcc>Accp.A1908T
COADREAD84179005441790054+Missense_MutationSNPCCTTCGA-AD-6889-01A-11D-1924-10TCGA-AD-6889-10A-01D-1924-10g.chr8:41790054C>Tc.5684G>Ac.(5683-5685)cGt>cAtp.R1895H
COADREAD84179007041790070+Missense_MutationSNPCCTTCGA-AZ-4682-01B-01D-1408-10TCGA-AZ-4682-10A-01D-1408-10g.chr8:41790070C>Tc.5668G>Ac.(5668-5670)Gca>Acap.A1890T
COADREAD84179049341790493+Missense_MutationSNPCCTTCGA-G4-6625-01A-21D-1771-10TCGA-G4-6625-11A-01D-1771-10g.chr8:41790493C>Tc.5245G>Ac.(5245-5247)Gcc>Accp.A1749T
COADREAD84179057341790573+Missense_MutationSNPTTGTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:41790573T>Gc.5165A>Cc.(5164-5166)gAa>gCap.E1722A
COADREAD84179065941790660+Frame_Shift_InsINS--GTCGA-AZ-6598-01A-11D-1771-10TCGA-AZ-6598-11A-01D-1771-10g.chr8:41790659_41790660insGc.5078_5079insCc.(5077-5079)ccafsp.P1693fs
COADREAD84179067441790674+SilentSNPCCTTCGA-AA-3715-01A-01W-0900-09TCGA-AA-3715-10A-01W-0900-09g.chr8:41790674C>Tc.5064G>Ac.(5062-5064)caG>caAp.Q1688Q
COADREAD84179125141791251+Missense_MutationSNPGGATCGA-AA-A00N-01A-02W-A00E-09TCGA-AA-A00N-10A-01W-A00E-09g.chr8:41791251G>Ac.4487C>Tc.(4486-4488)tCg>tTgp.S1496L
COADREAD84179131141791311+Missense_MutationSNPGGATCGA-AA-A00A-01A-01W-A005-10TCGA-AA-A00A-10A-01W-A005-10g.chr8:41791311G>Ac.4427C>Tc.(4426-4428)gCg>gTgp.A1476V
COADREAD84179151641791516+Missense_MutationSNPCCTTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:41791516C>Tc.4222G>Ac.(4222-4224)Gaa>Aaap.E1408K
COADREAD84179201141792011+Frame_Shift_DelDELCC-TCGA-CM-4743-01A-01D-1719-10TCGA-CM-4743-10A-01D-1719-10g.chr8:41792011delCc.3727delGc.(3727-3729)gatfsp.D1243fs
COADREAD84179214541792145+Missense_MutationSNPGGATCGA-AA-3989-01A-01W-0995-10TCGA-AA-3989-10A-01W-0999-10g.chr8:41792145G>Ac.3593C>Tc.(3592-3594)gCt>gTtp.A1198V
COADREAD84179492541794925+SilentSNPGGATCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr8:41794925G>Ac.3201C>Tc.(3199-3201)atC>atTp.I1067I
COADREAD84179846941798469+Missense_MutationSNPTTCTCGA-AA-3525-01A-02W-0833-10TCGA-AA-3525-10A-01W-0833-10g.chr8:41798469T>Cc.2930A>Gc.(2929-2931)gAc>gGcp.D977G
COADREAD84179848441798484+Missense_MutationSNPCCTTCGA-AA-A00N-01A-02W-A00E-09TCGA-AA-A00N-10A-01W-A00E-09g.chr8:41798484C>Tc.2915G>Ac.(2914-2916)cGc>cAcp.R972H
COADREAD84179848741798487+Missense_MutationSNPCCTTCGA-CM-6171-01A-11D-1650-10TCGA-CM-6171-10A-01D-1650-10g.chr8:41798487C>Tc.2912G>Ac.(2911-2913)cGt>cAtp.R971H
COADREAD84179849541798495+SilentSNPCCTTCGA-D5-6930-01A-11D-1924-10TCGA-D5-6930-10A-01D-1924-10g.chr8:41798495C>Tc.2904G>Ac.(2902-2904)agG>agAp.R968R
COADREAD84179880841798808+Missense_MutationSNPCCTTCGA-AA-3710-01A-01W-0995-10TCGA-AA-3710-10A-01W-0995-10g.chr8:41798808C>Tc.2591G>Ac.(2590-2592)cGg>cAgp.R864Q
COADREAD84179892641798926+Missense_MutationSNPCCATCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:41798926C>Ac.2473G>Tc.(2473-2475)Gat>Tatp.D825Y
COADREAD84179894741798947+Missense_MutationSNPAAGTCGA-AA-A01Q-01A-01W-A005-10TCGA-AA-A01Q-10A-01W-A005-10g.chr8:41798947A>Gc.2452T>Cc.(2452-2454)Tct>Cctp.S818P
COADREAD84180147541801475+Missense_MutationSNPTTATCGA-AA-3663-01A-01D-1719-10TCGA-AA-3663-11A-01D-1719-10g.chr8:41801475T>Ac.2019A>Tc.(2017-2019)gaA>gaTp.E673D
COADREAD84180147541801475+SilentSNPTTCTCGA-AU-3779-01A-01D-1719-10TCGA-AU-3779-10A-01D-1719-10g.chr8:41801475T>Cc.2019A>Gc.(2017-2019)gaA>gaGp.E673E
COADREAD84180147741801477+Nonsense_MutationSNPCCATCGA-A6-5661-01A-01D-1650-10TCGA-A6-5661-10A-01D-1650-10g.chr8:41801477C>Ac.2017G>Tc.(2017-2019)Gaa>Taap.E673*
COADREAD84180411541804115+Missense_MutationSNPCCTTCGA-AA-A00N-01A-02W-A00E-09TCGA-AA-A00N-10A-01W-A00E-09g.chr8:41804115C>Tc.1990G>Ac.(1990-1992)Gat>Aatp.D664N
COADREAD84180411541804115+Missense_MutationSNPCCTTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr8:41804115C>Tc.1990G>Ac.(1990-1992)Gat>Aatp.D664N
COADREAD84180541741805417+Missense_MutationSNPAAGTCGA-A6-5665-01A-01D-1650-10TCGA-A6-5665-10A-01D-1650-10g.chr8:41805417A>Gc.1754T>Cc.(1753-1755)gTg>gCgp.V585A
COADREAD84180541741805417+Missense_MutationSNPAAGTCGA-G4-6303-01A-11D-1771-10TCGA-G4-6303-10A-01D-1771-10g.chr8:41805417A>Gc.1754T>Cc.(1753-1755)gTg>gCgp.V585A
COADREAD84180676541806765+Missense_MutationSNPCCATCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:41806765C>Ac.1715G>Tc.(1714-1716)aGa>aTap.R572I
COADREAD84181283741812837+SilentSNPGGATCGA-AD-5900-01A-11D-1650-10TCGA-AD-5900-10A-01D-1650-10g.chr8:41812837G>Ac.1575C>Tc.(1573-1575)tcC>tcTp.S525S
COADREAD84181284041812840+SilentSNPGGATCGA-F4-6807-01A-11D-1835-10TCGA-F4-6807-10A-01D-1835-10g.chr8:41812840G>Ac.1572C>Tc.(1570-1572)tcC>tcTp.S524S
COADREAD84183233641832336+SilentSNPAAGTCGA-DM-A28K-01A-21D-A16V-10TCGA-DM-A28K-10A-01D-A16V-10g.chr8:41832336A>Gc.1368T>Cc.(1366-1368)aaT>aaCp.N456N
COADREAD84183233741832337+Missense_MutationSNPTTCTCGA-AZ-6607-01A-11D-1835-10TCGA-AZ-6607-11A-01D-1835-10g.chr8:41832337T>Cc.1367A>Gc.(1366-1368)aAt>aGtp.N456S
COADREAD84183233741832337+Missense_MutationSNPTTCTCGA-DM-A28E-01A-11D-A16V-10TCGA-DM-A28E-10A-01D-A16V-10g.chr8:41832337T>Cc.1367A>Gc.(1366-1368)aAt>aGtp.N456S
COADREAD84183233741832337+Missense_MutationSNPTTCTCGA-G4-6315-01A-11D-1719-10TCGA-G4-6315-10A-01D-1720-10g.chr8:41832337T>Cc.1367A>Gc.(1366-1368)aAt>aGtp.N456S
COADREAD84183233841832338+Missense_MutationSNPTTCTCGA-DC-6681-01A-11D-1826-10TCGA-DC-6681-10A-01D-1826-10g.chr8:41832338T>Cc.1366A>Gc.(1366-1368)Aat>Gatp.N456D
COADREAD84183457641834576+Missense_MutationSNPCCTTCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr8:41834576C>Tc.1313G>Ac.(1312-1314)cGa>cAap.R438Q
COADREAD84183481941834819+Missense_MutationSNPCCTTCGA-AG-A02N-01A-11W-A096-10TCGA-AG-A02N-11A-11W-A096-10g.chr8:41834819C>Tc.1070G>Ac.(1069-1071)cGa>cAap.R357Q
COADREAD84183616241836162+SilentSNPCCTTCGA-CM-4746-01A-01D-1408-10TCGA-CM-4746-10A-01D-1408-10g.chr8:41836162C>Tc.1041G>Ac.(1039-1041)acG>acAp.T347T
COADREAD84183621541836215+Missense_MutationSNPGGATCGA-AA-3949-01A-01W-0995-10TCGA-AA-3949-10A-01W-0995-10g.chr8:41836215G>Ac.988C>Tc.(988-990)Cgc>Tgcp.R330C
COADREAD84190626041906260+Missense_MutationSNPCCTTCGA-AA-3977-01A-01W-0995-10TCGA-AA-3977-10A-01W-0999-10g.chr8:41906260C>Tc.236G>Ac.(235-237)cGa>cAap.R79Q
COADREAD84190636541906365+Missense_MutationSNPCCTTCGA-AA-3525-01A-02W-0833-10TCGA-AA-3525-10A-01W-0833-10g.chr8:41906365C>Tc.131G>Ac.(130-132)cGt>cAtp.R44H
DLBC84179086641790866+SilentSNPGGCTCGA-G8-6325-01A-11D-2210-10TCGA-G8-6325-10A-01D-2210-10g.chr8:41790866G>Cc.4872C>Gc.(4870-4872)gtC>gtGp.V1624V
DLBC84183460041834600+Missense_MutationSNPAAGTCGA-VB-A8QN-01A-11D-A382-10TCGA-VB-A8QN-10A-01D-A385-10g.chr8:41834600A>Gc.1289T>Cc.(1288-1290)gTg>gCgp.V430A
ESCA84179030041790300+Missense_MutationSNPGGTTCGA-RE-A7BO-01A-11D-A33E-09TCGA-RE-A7BO-10A-01D-A33H-09g.chr8:41790300G>Tc.5438C>Ac.(5437-5439)cCc>cAcp.P1813H
ESCA84179138241791382+SilentSNPCCTTCGA-IG-A7DP-01A-31D-A33E-09TCGA-IG-A7DP-10A-01D-A33H-09g.chr8:41791382C>Tc.4356G>Ac.(4354-4356)gcG>gcAp.A1452A
ESCA84179158841791588+Missense_MutationSNPCCTTCGA-L5-A8NM-01A-11D-A37C-09TCGA-L5-A8NM-11A-12D-A37F-09g.chr8:41791588C>Tc.4150G>Ac.(4150-4152)Gtg>Atgp.V1384M
ESCA84179200741792007+Missense_MutationSNPGGATCGA-L5-A88W-01A-11D-A351-09TCGA-L5-A88W-11A-11D-A351-09g.chr8:41792007G>Ac.3731C>Tc.(3730-3732)gCa>gTap.A1244V
ESCA84179862041798620+Missense_MutationSNPGGATCGA-L5-A4OW-01A-11D-A28B-09TCGA-L5-A4OW-11A-11D-A28E-09g.chr8:41798620G>Ac.2779C>Tc.(2779-2781)Cca>Tcap.P927S
ESCA84180050141800501+Missense_MutationSNPCCTTCGA-JY-A93D-01A-11D-A387-09TCGA-JY-A93D-10A-01D-A38A-09g.chr8:41800501C>Tc.2246G>Ac.(2245-2247)cGg>cAgp.R749Q
ESCA84180677341806773+SilentSNPCCTTCGA-LN-A4A9-01A-11D-A28B-09TCGA-LN-A4A9-10A-01D-A28E-09g.chr8:41806773C>Tc.1707G>Ac.(1705-1707)gaG>gaAp.E569E
ESCA84183621741836217+Missense_MutationSNPCCTTCGA-XP-A8T6-01A-11D-A36J-09TCGA-XP-A8T6-10A-01D-A36M-09g.chr8:41836217C>Tc.986G>Ac.(985-987)cGg>cAgp.R329Q
ESCA84183622341836223+Missense_MutationSNPAAGTCGA-L5-A88S-01A-11D-A36J-09TCGA-L5-A88S-11A-21D-A36M-09g.chr8:41836223A>Gc.980T>Cc.(979-981)aTa>aCap.I327T
ESCA84183837041838370+Missense_MutationSNPGGATCGA-L5-A8NF-01A-11D-A37C-09TCGA-L5-A8NF-11A-11D-A37F-09g.chr8:41838370G>Ac.901C>Tc.(901-903)Cca>Tcap.P301S
ESCA84183838841838388+Missense_MutationSNPGGTTCGA-L5-A4OI-01A-11D-A27G-09TCGA-L5-A4OI-11A-11D-A27G-09g.chr8:41838388G>Tc.883C>Ac.(883-885)Ccg>Acgp.P295T
GBMLGG84179065941790659+SilentSNPTTGTCGA-HT-7477-01B-11D-A289-08TCGA-HT-7477-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-HT-8015-01B-11D-A289-08TCGA-HT-8015-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-HT-8111-01A-11D-2395-08TCGA-HT-8111-10A-01D-2396-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-HT-A5R5-01A-11D-A289-08TCGA-HT-A5R5-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-HT-A5RA-01A-11D-A289-08TCGA-HT-A5RA-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-P5-A5F0-01A-11D-A289-08TCGA-P5-A5F0-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-P5-A5F1-01A-11D-A289-08TCGA-P5-A5F1-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-P5-A5F2-01A-11D-A289-08TCGA-P5-A5F2-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-P5-A5F4-01A-11D-A289-08TCGA-P5-A5F4-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179065941790659+SilentSNPTTGTCGA-P5-A5F6-01A-11D-A289-08TCGA-P5-A5F6-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
GBMLGG84179121941791219+Missense_MutationSNPTTCTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr8:41791219T>Cc.4519A>Gc.(4519-4521)Agt>Ggtp.S1507G
GBMLGG84179127741791277+Missense_MutationSNPCCATCGA-S9-A6U0-01A-12D-A32B-08TCGA-S9-A6U0-10A-01D-A329-08g.chr8:41791277C>Ac.4461G>Tc.(4459-4461)caG>caTp.Q1487H
GBMLGG84179868141798681+SilentSNPTTCTCGA-HT-A74K-01A-11D-A32B-08TCGA-HT-A74K-10A-01D-A329-08g.chr8:41798681T>Cc.2718A>Gc.(2716-2718)tcA>tcGp.S906S
GBMLGG84183936841839368+Missense_MutationSNPCCATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr8:41839368C>Ac.814G>Tc.(814-816)Ggc>Tgcp.G272C
HNSC84179131041791310+SilentSNPCCTTCGA-CN-6994-01A-11D-1912-08TCGA-CN-6994-10A-01D-1912-08g.chr8:41791310C>Tc.4428G>Ac.(4426-4428)gcG>gcAp.A1476A
HNSC84179150741791507+Missense_MutationSNPCCGTCGA-CR-7371-01A-11D-2012-08TCGA-CR-7371-10A-01D-2013-08g.chr8:41791507C>Gc.4231G>Cc.(4231-4233)Gag>Cagp.E1411Q
HNSC84179163141791631+SilentSNPGGATCGA-CV-6953-01A-11D-1912-08TCGA-CV-6953-10A-01D-1912-08g.chr8:41791631G>Ac.4107C>Tc.(4105-4107)acC>acTp.T1369T
HNSC84179196241791962+Missense_MutationSNPTTCTCGA-IQ-A6SH-01A-12D-A34J-08TCGA-IQ-A6SH-10A-01D-A34M-08g.chr8:41791962T>Cc.3776A>Gc.(3775-3777)aAt>aGtp.N1259S
HNSC84179208141792081+SilentSNPTTCTCGA-CR-7374-01A-11D-2012-08TCGA-CR-7374-10A-01D-2013-08g.chr8:41792081T>Cc.3657A>Gc.(3655-3657)ctA>ctGp.L1219L
HNSC84179229441792294+Frame_Shift_DelDELCC-TCGA-CN-4731-01A-01D-1434-08TCGA-CN-4731-10A-01D-1434-08g.chr8:41792294delCc.3444delGc.(3442-3444)aagfsp.K1150fs
HNSC84179856941798569+Frame_Shift_DelDELCC-TCGA-CN-5369-01A-01D-1434-08TCGA-CN-5369-10A-01D-1434-08g.chr8:41798569delCc.2830delGc.(2830-2832)gttfsp.V944fs
HNSC84179873841798738+SilentSNPGGCTCGA-CR-7371-01A-11D-2012-08TCGA-CR-7371-10A-01D-2013-08g.chr8:41798738G>Cc.2661C>Gc.(2659-2661)ctC>ctGp.L887L
HNSC84179881441798814+Missense_MutationSNPGGATCGA-D6-6516-01A-11D-1870-08TCGA-D6-6516-10A-01D-1870-08g.chr8:41798814G>Ac.2585C>Tc.(2584-2586)cCa>cTap.P862L
HNSC84179887041798870+SilentSNPAAGTCGA-F7-A624-01A-22D-A30E-08TCGA-F7-A624-10A-01D-A30H-08g.chr8:41798870A>Gc.2529T>Cc.(2527-2529)tcT>tcCp.S843S
HNSC84180135241801352+Missense_MutationSNPCCGTCGA-UF-A7JT-01A-11D-A34J-08TCGA-UF-A7JT-10A-01D-A34M-08g.chr8:41801352C>Gc.2142G>Cc.(2140-2142)aaG>aaCp.K714N
HNSC84183625341836253+Missense_MutationSNPCCGTCGA-CR-7364-01A-11D-2012-08TCGA-CR-7364-10A-01D-2013-08g.chr8:41836253C>Gc.950G>Cc.(949-951)cGa>cCap.R317P
HNSC84183936441839364+Missense_MutationSNPTTCTCGA-F7-A624-01A-22D-A30E-08TCGA-F7-A624-10A-01D-A30H-08g.chr8:41839364T>Cc.818A>Gc.(817-819)aAa>aGap.K273R
KIPAN84179017241790172+Missense_MutationSNPAAGTCGA-2K-A9WE-01A-11D-A382-10TCGA-2K-A9WE-10A-01D-A385-10g.chr8:41790172A>Gc.5566T>Cc.(5566-5568)Tcc>Cccp.S1856P
KIPAN84179040541790405+Missense_MutationSNPGGTTCGA-BP-5181-01A-01D-1429-08TCGA-BP-5181-11A-01D-1429-08g.chr8:41790405G>Tc.5333C>Ac.(5332-5334)aCt>aAtp.T1778N
KIPAN84179180041791800+Missense_MutationSNPTTCTCGA-BP-4167-01A-02D-1386-10TCGA-BP-4167-11A-01D-1251-10g.chr8:41791800T>Cc.3938A>Gc.(3937-3939)gAc>gGcp.D1313G
KIPAN84179194241791942+Missense_MutationSNPTTGTCGA-DW-7837-01A-11D-2136-08TCGA-DW-7837-10A-01D-2136-08g.chr8:41791942T>Gc.3796A>Cc.(3796-3798)Aag>Cagp.K1266Q
KIPAN84179228941792289+Missense_MutationSNPTTGTCGA-CZ-4853-01A-01D-1429-08TCGA-CZ-4853-11A-01D-1429-08g.chr8:41792289T>Gc.3449A>Cc.(3448-3450)aAg>aCgp.K1150T
KIPAN84179492841794928+Missense_MutationSNPCCATCGA-B9-5155-01A-01D-1589-08TCGA-B9-5155-10A-01D-1589-08g.chr8:41794928C>Ac.3198G>Tc.(3196-3198)gaG>gaTp.E1066D
KIPAN84179494541794945+Missense_MutationSNPAATTCGA-HE-A5NK-01A-11D-A26P-10TCGA-HE-A5NK-10A-01D-A26P-10g.chr8:41794945A>Tc.3181T>Ac.(3181-3183)Tta>Atap.L1061I
KIPAN84180127541801275+Missense_MutationSNPCCATCGA-BP-4177-01A-02D-1421-08TCGA-BP-4177-11A-01D-1421-08g.chr8:41801275C>Ac.2219G>Tc.(2218-2220)cGt>cTtp.R740L
KIPAN84180411741804117+Missense_MutationSNPAAGTCGA-B0-5710-01A-11D-1669-08TCGA-B0-5710-11A-01D-1669-08g.chr8:41804117A>Gc.1988T>Cc.(1987-1989)aTc>aCcp.I663T
KIPAN84183616141836161+Splice_SiteDELCC-TCGA-BQ-7046-01A-11D-1961-08TCGA-BQ-7046-11A-01D-1961-08g.chr8:41836161delCc.1042delGc.(1042-1044)gta>tap.V348fs
KIPAN84183621841836218+Missense_MutationSNPGGATCGA-B0-5099-01A-01D-1421-08TCGA-B0-5099-11A-01D-1421-08g.chr8:41836218G>Ac.985C>Tc.(985-987)Cgg>Tggp.R329W
KIPAN84190630541906305+Nonsense_MutationSNPGGTTCGA-2Z-A9J2-01A-11D-A382-10TCGA-2Z-A9J2-10A-01D-A385-10g.chr8:41906305G>Tc.191C>Ac.(190-192)tCa>tAap.S64*
KIRC84179040541790405+Missense_MutationSNPGGTTCGA-BP-5181-01A-01D-1429-08TCGA-BP-5181-11A-01D-1429-08g.chr8:41790405G>Tc.5333C>Ac.(5332-5334)aCt>aAtp.T1778N
KIRC84179180041791800+Missense_MutationSNPTTCTCGA-BP-4167-01A-02D-1386-10TCGA-BP-4167-11A-01D-1251-10g.chr8:41791800T>Cc.3938A>Gc.(3937-3939)gAc>gGcp.D1313G
KIRC84179228941792289+Missense_MutationSNPTTGTCGA-CZ-4853-01A-01D-1429-08TCGA-CZ-4853-11A-01D-1429-08g.chr8:41792289T>Gc.3449A>Cc.(3448-3450)aAg>aCgp.K1150T
KIRC84180127541801275+Missense_MutationSNPCCATCGA-BP-4177-01A-02D-1421-08TCGA-BP-4177-11A-01D-1421-08g.chr8:41801275C>Ac.2219G>Tc.(2218-2220)cGt>cTtp.R740L
KIRC84180411741804117+Missense_MutationSNPAAGTCGA-B0-5710-01A-11D-1669-08TCGA-B0-5710-11A-01D-1669-08g.chr8:41804117A>Gc.1988T>Cc.(1987-1989)aTc>aCcp.I663T
KIRC84183621841836218+Missense_MutationSNPGGATCGA-B0-5099-01A-01D-1421-08TCGA-B0-5099-11A-01D-1421-08g.chr8:41836218G>Ac.985C>Tc.(985-987)Cgg>Tggp.R329W
KIRP84179017241790172+Missense_MutationSNPAAGTCGA-2K-A9WE-01A-11D-A382-10TCGA-2K-A9WE-10A-01D-A385-10g.chr8:41790172A>Gc.5566T>Cc.(5566-5568)Tcc>Cccp.S1856P
KIRP84179194241791942+Missense_MutationSNPTTGTCGA-DW-7837-01A-11D-2136-08TCGA-DW-7837-10A-01D-2136-08g.chr8:41791942T>Gc.3796A>Cc.(3796-3798)Aag>Cagp.K1266Q
KIRP84179492841794928+Missense_MutationSNPCCATCGA-B9-5155-01A-01D-1589-08TCGA-B9-5155-10A-01D-1589-08g.chr8:41794928C>Ac.3198G>Tc.(3196-3198)gaG>gaTp.E1066D
KIRP84179494541794945+Missense_MutationSNPAATTCGA-HE-A5NK-01A-11D-A26P-10TCGA-HE-A5NK-10A-01D-A26P-10g.chr8:41794945A>Tc.3181T>Ac.(3181-3183)Tta>Atap.L1061I
KIRP84183616141836161+Splice_SiteDELCC-TCGA-BQ-7046-01A-11D-1961-08TCGA-BQ-7046-11A-01D-1961-08g.chr8:41836161delCc.1042delGc.(1042-1044)gta>tap.V348fs
KIRP84190630541906305+Nonsense_MutationSNPGGTTCGA-2Z-A9J2-01A-11D-A382-10TCGA-2Z-A9J2-10A-01D-A385-10g.chr8:41906305G>Tc.191C>Ac.(190-192)tCa>tAap.S64*
LGG84179065941790659+SilentSNPTTGTCGA-HT-7477-01B-11D-A289-08TCGA-HT-7477-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-HT-8015-01B-11D-A289-08TCGA-HT-8015-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-HT-8111-01A-11D-2395-08TCGA-HT-8111-10A-01D-2396-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-HT-A5R5-01A-11D-A289-08TCGA-HT-A5R5-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-HT-A5RA-01A-11D-A289-08TCGA-HT-A5RA-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-P5-A5F0-01A-11D-A289-08TCGA-P5-A5F0-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-P5-A5F1-01A-11D-A289-08TCGA-P5-A5F1-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-P5-A5F2-01A-11D-A289-08TCGA-P5-A5F2-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-P5-A5F4-01A-11D-A289-08TCGA-P5-A5F4-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179065941790659+SilentSNPTTGTCGA-P5-A5F6-01A-11D-A289-08TCGA-P5-A5F6-10A-01D-A289-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LGG84179121941791219+Missense_MutationSNPTTCTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr8:41791219T>Cc.4519A>Gc.(4519-4521)Agt>Ggtp.S1507G
LGG84179127741791277+Missense_MutationSNPCCATCGA-S9-A6U0-01A-12D-A32B-08TCGA-S9-A6U0-10A-01D-A329-08g.chr8:41791277C>Ac.4461G>Tc.(4459-4461)caG>caTp.Q1487H
LGG84179868141798681+SilentSNPTTCTCGA-HT-A74K-01A-11D-A32B-08TCGA-HT-A74K-10A-01D-A329-08g.chr8:41798681T>Cc.2718A>Gc.(2716-2718)tcA>tcGp.S906S
LGG84183936841839368+Missense_MutationSNPCCATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr8:41839368C>Ac.814G>Tc.(814-816)Ggc>Tgcp.G272C
LIHC84179060741790607+Missense_MutationSNPAAGTCGA-EP-A2KA-01A-11D-A183-10TCGA-EP-A2KA-10A-01D-A183-10g.chr8:41790607A>Gc.5131T>Cc.(5131-5133)Ttc>Ctcp.F1711L
LIHC84179142241791422+Missense_MutationSNPTTCTCGA-DD-A119-01A-11D-A12Z-10TCGA-DD-A119-10A-01D-A12Z-10g.chr8:41791422T>Cc.4316A>Gc.(4315-4317)cAt>cGtp.H1439R
LIHC84179155141791551+Missense_MutationSNPTTCTCGA-CC-A3MB-01A-11D-A20W-10TCGA-CC-A3MB-10A-01D-A20W-10g.chr8:41791551T>Cc.4187A>Gc.(4186-4188)cAc>cGcp.H1396R
LIHC84179168341791683+Frame_Shift_DelDELAA-TCGA-G3-A3CJ-01A-11D-A20W-10TCGA-G3-A3CJ-10A-01D-A20W-10g.chr8:41791683delAc.4055delTc.(4054-4056)ttafsp.L1352fs
LIHC84179222841792228+Frame_Shift_DelDELTT-TCGA-G3-A3CJ-01A-11D-A20W-10TCGA-G3-A3CJ-10A-01D-A20W-10g.chr8:41792228delTc.3510delAc.(3508-3510)aaafsp.K1170fs
LIHC84179479941794799+Missense_MutationSNPTTATCGA-DD-A119-01A-11D-A12Z-10TCGA-DD-A119-10A-01D-A12Z-10g.chr8:41794799T>Ac.3327A>Tc.(3325-3327)gaA>gaTp.E1109D
LIHC84179861441798614+Nonsense_MutationSNPGGATCGA-DD-AAE6-01A-11D-A40R-10TCGA-DD-AAE6-10A-01D-A40U-10g.chr8:41798614G>Ac.2785C>Tc.(2785-2787)Cag>Tagp.Q929*
LIHC84180529441805294+Missense_MutationSNPCCATCGA-DD-AAD1-01A-11D-A40R-10TCGA-DD-AAD1-10A-01D-A40U-10g.chr8:41805294C>Ac.1877G>Tc.(1876-1878)tGc>tTcp.C626F
LIHC84181289741812897+SilentSNPTTCTCGA-WX-AA46-01A-11D-A38X-10TCGA-WX-AA46-10A-01D-A38X-10g.chr8:41812897T>Cc.1515A>Gc.(1513-1515)caA>caGp.Q505Q
LIHC84183229141832291+Frame_Shift_DelDELAA-TCGA-DD-A39Y-01A-11D-A20W-10TCGA-DD-A39Y-11A-11D-A20W-10g.chr8:41832291delAc.1413delTc.(1411-1413)tttfsp.F471fs
LIHC84190592541905925+Missense_MutationSNPCCATCGA-DD-AADM-01A-11D-A40R-10TCGA-DD-AADM-10A-01D-A40U-10g.chr8:41905925C>Ac.571G>Tc.(571-573)Gtg>Ttgp.V191L
LIHC84190623341906233+Missense_MutationSNPTTATCGA-DD-AADP-01A-11D-A38X-10TCGA-DD-AADP-10A-01D-A38X-10g.chr8:41906233T>Ac.263A>Tc.(262-264)cAt>cTtp.H88L
LIHC84190638741906387+Missense_MutationSNPAAGTCGA-ES-A2HT-01A-12D-A183-10TCGA-ES-A2HT-11A-11D-A183-10g.chr8:41906387A>Gc.109T>Cc.(109-111)Tct>Cctp.S37P
LUAD84178990341789903+Missense_MutationSNPCCATCGA-17-Z057-01A-01W-0747-08TCGA-17-Z057-11A-01W-0747-08g.chr8:41789903C>Ac.5835G>Tc.(5833-5835)caG>caTp.Q1945H
LUAD84179029941790299+SilentSNPGGATCGA-75-6214-01A-41D-1945-08TCGA-75-6214-10A-01D-1946-08g.chr8:41790299G>Ac.5439C>Tc.(5437-5439)ccC>ccTp.P1813P
LUAD84179045241790452+SilentSNPGGATCGA-17-Z028-01A-01W-0746-08TCGA-17-Z028-11A-01W-0746-08g.chr8:41790452G>Ac.5286C>Tc.(5284-5286)acC>acTp.T1762T
LUAD84179058341790583+Missense_MutationSNPCCTTCGA-NJ-A4YP-01A-11D-A25L-08TCGA-NJ-A4YP-10A-01D-A25L-08g.chr8:41790583C>Tc.5155G>Ac.(5155-5157)Gag>Aagp.E1719K
LUAD84179065941790659+SilentSNPTTGTCGA-78-8662-01A-11D-2393-08TCGA-78-8662-10A-01D-2393-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LUAD84179065941790659+SilentSNPTTGTCGA-86-8672-01A-21D-2393-08TCGA-86-8672-10A-01D-2393-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LUAD84179065941790659+SilentSNPTTGTCGA-86-8673-01A-11D-2393-08TCGA-86-8673-10A-01D-2393-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LUAD84179065941790659+SilentSNPTTGTCGA-97-8547-01A-11D-2393-08TCGA-97-8547-10A-01D-2393-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
LUAD84179119541791195+Missense_MutationSNPCCTTCGA-86-8056-01A-11D-2238-08TCGA-86-8056-10A-01D-2238-08g.chr8:41791195C>Tc.4543G>Ac.(4543-4545)Gaa>Aaap.E1515K
LUAD84179138241791382+SilentSNPCCATCGA-49-4494-01A-01D-1265-08TCGA-49-4494-11A-01D-1265-08g.chr8:41791382C>Ac.4356G>Tc.(4354-4356)gcG>gcTp.A1452A
LUAD84179140841791408+Nonsense_MutationSNPGGATCGA-49-6745-01A-11D-1855-08TCGA-49-6745-11A-01D-1855-08g.chr8:41791408G>Ac.4330C>Tc.(4330-4332)Cag>Tagp.Q1444*
LUAD84179142041791420+Nonsense_MutationSNPCCATCGA-78-7149-01A-11D-2036-08TCGA-78-7149-10A-01D-2036-08g.chr8:41791420C>Ac.4318G>Tc.(4318-4320)Gag>Tagp.E1440*
LUAD84179142641791426+Nonsense_MutationSNPCCATCGA-L9-A444-01A-21D-A24D-08TCGA-L9-A444-10A-01D-A24F-08g.chr8:41791426C>Ac.4312G>Tc.(4312-4314)Gag>Tagp.E1438*
LUAD84179183141791831+Missense_MutationSNPCCATCGA-62-8399-01A-21D-2323-08TCGA-62-8399-10A-01D-2323-08g.chr8:41791831C>Ac.3907G>Tc.(3907-3909)Gat>Tatp.D1303Y
LUAD84179228241792282+Nonsense_MutationSNPCCTTCGA-50-5941-01A-11D-1753-08TCGA-50-5941-10A-01D-1753-08g.chr8:41792282C>Tc.3456G>Ac.(3454-3456)tgG>tgAp.W1152*
LUAD84179235941792359+Missense_MutationSNPGGATCGA-97-7941-01A-11D-2184-08TCGA-97-7941-10A-01D-2184-08g.chr8:41792359G>Ac.3379C>Tc.(3379-3381)Ctt>Tttp.L1127F
LUAD84179483541794835+Missense_MutationSNPCCATCGA-44-7667-01A-31D-2063-08TCGA-44-7667-10A-01D-2063-08g.chr8:41794835C>Ac.3291G>Tc.(3289-3291)caG>caTp.Q1097H
LUAD84180533941805339+Missense_MutationSNPTTATCGA-69-A59K-01A-11D-A25L-08TCGA-69-A59K-10A-01D-A25L-08g.chr8:41805339T>Ac.1832A>Tc.(1831-1833)gAg>gTgp.E611V
LUAD84181283641812836+Missense_MutationSNPGGTTCGA-55-8511-01A-11D-2393-08TCGA-55-8511-10A-01D-2393-08g.chr8:41812836G>Tc.1576C>Ac.(1576-1578)Cca>Acap.P526T
LUAD84183458441834584+SilentSNPCCTTCGA-67-3771-01A-01D-1040-01TCGA-67-3771-10A-01D-1040-01g.chr8:41834584C>Tc.1305G>Ac.(1303-1305)gaG>gaAp.E435E
LUAD84183624541836245+SilentSNPGGATCGA-MP-A4T4-01A-11D-A25L-08TCGA-MP-A4T4-10A-01D-A25L-08g.chr8:41836245G>Ac.958C>Tc.(958-960)Cta>Ttap.L320L
LUAD84183629741836297+Splice_SiteSNPTTATCGA-50-5049-01A-01D-1625-08TCGA-50-5049-10A-01D-1625-08g.chr8:41836297T>Ac.e7-2
LUAD84183944641839446+Missense_MutationSNPGGCTCGA-55-8616-01A-11D-2393-08TCGA-55-8616-10A-01D-2393-08g.chr8:41839446G>Cc.736C>Gc.(736-738)Cct>Gctp.P246A
LUAD84190626741906267+Missense_MutationSNPGGCTCGA-MP-A4TA-01A-21D-A24P-08TCGA-MP-A4TA-10A-01D-A24P-08g.chr8:41906267G>Cc.229C>Gc.(229-231)Cct>Gctp.P77A
LUSC84179017541790175+Missense_MutationSNPTTATCGA-39-5031-01A-01D-1441-08TCGA-39-5031-11A-01D-1441-08g.chr8:41790175T>Ac.5563A>Tc.(5563-5565)Att>Tttp.I1855F
LUSC84179120641791206+Missense_MutationSNPTTATCGA-56-6545-01A-11D-1817-08TCGA-56-6545-10A-01D-1817-08g.chr8:41791206T>Ac.4532A>Tc.(4531-4533)cAg>cTgp.Q1511L
LUSC84179216241792162+SilentSNPGGATCGA-85-6560-01A-11D-1817-08TCGA-85-6560-10A-01D-1817-08g.chr8:41792162G>Ac.3576C>Tc.(3574-3576)atC>atTp.I1192I
LUSC84179840341798403+Nonsense_MutationSNPGGCTCGA-34-2600-01A-01D-1522-08TCGA-34-2600-11A-01D-1522-08g.chr8:41798403G>Cc.2996C>Gc.(2995-2997)tCa>tGap.S999*
LUSC84179877041798770+Nonsense_MutationSNPCCATCGA-60-2720-01A-01D-1522-08TCGA-60-2720-11A-01D-1522-08g.chr8:41798770C>Ac.2629G>Tc.(2629-2631)Gaa>Taap.E877*
LUSC84180048841800488+SilentSNPGGATCGA-18-3409-01A-01D-0983-08TCGA-18-3409-11A-01D-0983-08g.chr8:41800488G>Ac.2259C>Tc.(2257-2259)atC>atTp.I753I
LUSC84180415241804152+SilentSNPAACTCGA-46-3765-01A-01D-0983-08TCGA-46-3765-10A-01D-0983-08g.chr8:41804152A>Cc.1953T>Gc.(1951-1953)ccT>ccGp.P651P
LUSC84180687741806877+Missense_MutationSNPGGATCGA-18-5592-01A-01D-1632-08TCGA-18-5592-11A-11D-1632-08g.chr8:41806877G>Ac.1603C>Tc.(1603-1605)Ccc>Tccp.P535S
LUSC84183452741834527+Splice_SiteSNPTTATCGA-33-4586-01A-01D-1441-08TCGA-33-4586-11A-01D-1441-08g.chr8:41834527T>Ac.1362A>Tc.(1360-1362)acA>acTp.T454T
LUSC84183454941834549+Nonsense_MutationSNPGGCTCGA-66-2785-01A-01D-1522-08TCGA-66-2785-11A-01D-1522-08g.chr8:41834549G>Cc.1340C>Gc.(1339-1341)tCa>tGap.S447*
LUSC84183469941834699+Missense_MutationSNPTTCTCGA-33-4582-01A-01D-1441-08TCGA-33-4582-11A-01D-1441-08g.chr8:41834699T>Cc.1190A>Gc.(1189-1191)aAt>aGtp.N397S
LUSC84183478141834781+Missense_MutationSNPGGATCGA-22-5477-01A-01D-1632-08TCGA-22-5477-11A-11D-1632-08g.chr8:41834781G>Ac.1108C>Tc.(1108-1110)Ctt>Tttp.L370F
LUSC84183480241834802+Missense_MutationSNPCCATCGA-66-2785-01A-01D-1522-08TCGA-66-2785-11A-01D-1522-08g.chr8:41834802C>Ac.1087G>Tc.(1087-1089)Ggt>Tgtp.G363C
LUSC84183838841838388+Missense_MutationSNPGGCTCGA-66-2785-01A-01D-1522-08TCGA-66-2785-11A-01D-1522-08g.chr8:41838388G>Cc.883C>Gc.(883-885)Ccg>Gcgp.P295A
LUSC84184505941845059+Missense_MutationSNPAAGTCGA-18-3408-01A-01D-0983-08TCGA-18-3408-11A-01D-0983-08g.chr8:41845059A>Gc.623T>Cc.(622-624)aTc>aCcp.I208T
OV84179147741791477+Missense_MutationSNPCCGTCGA-61-1727-01A-01W-0639-09TCGA-61-1727-11A-01W-0639-09g.chr8:41791477C>Gc.4261G>Cc.(4261-4263)Gat>Catp.D1421H
OV84179221141792211+Missense_MutationSNPCCGTCGA-23-2645-01A-01W-1091-09TCGA-23-2645-10A-01W-1091-09g.chr8:41792211C>Gc.3527G>Cc.(3526-3528)aGt>aCtp.S1176T
OV84180147541801475+Missense_MutationSNPTTGTCGA-13-0714-01A-01W-0370-10TCGA-13-0714-10B-01W-0370-10g.chr8:41801475T>Gc.2019A>Cc.(2017-2019)gaA>gaCp.E673D
OV84180541841805418+Missense_MutationSNPCCTTCGA-09-2049-01D-01W-0799-08TCGA-09-2049-10A-01W-0799-08g.chr8:41805418C>Tc.1753G>Ac.(1753-1755)Gtg>Atgp.V585M
OV84183233741832337+Missense_MutationSNPTTCTCGA-13-0904-01A-02W-0420-08TCGA-13-0904-10A-01D-0399-08g.chr8:41832337T>Cc.1367A>Gc.(1366-1368)aAt>aGtp.N456S
PAAD84179065941790659+SilentSNPTTGTCGA-2L-AAQI-01A-12D-A397-08TCGA-2L-AAQI-11A-11D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-2L-AAQJ-01A-12D-A397-08TCGA-2L-AAQJ-11A-11D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-3A-A9IB-01A-21D-A397-08TCGA-3A-A9IB-10A-01D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-3A-A9IH-01A-12D-A397-08TCGA-3A-A9IH-10A-01D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-3A-A9IS-01A-21D-A397-08TCGA-3A-A9IS-10A-01D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-3A-A9IU-01A-11D-A397-08TCGA-3A-A9IU-10A-01D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-FB-AAPS-01A-12D-A397-08TCGA-FB-AAPS-11A-11D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-HV-AA8X-01A-11D-A397-08TCGA-HV-AA8X-10A-01D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-IB-8126-01A-11D-2396-08TCGA-IB-8126-10A-01D-2396-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-RB-AA9M-01A-11D-A397-08TCGA-RB-AA9M-10A-01D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-US-A77G-01A-11D-A32N-08TCGA-US-A77G-11A-11D-A32N-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-US-A77J-01A-11D-A32N-08TCGA-US-A77J-11A-11D-A32N-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179065941790659+SilentSNPTTGTCGA-XD-AAUL-01A-21D-A397-08TCGA-XD-AAUL-10A-01D-A39A-08g.chr8:41790659T>Gc.5079A>Cc.(5077-5079)ccA>ccCp.P1693P
PAAD84179121941791219+Missense_MutationSNPTTGTCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr8:41791219T>Gc.4519A>Cc.(4519-4521)Agt>Cgtp.S1507R
PAAD84179480141794801+Missense_MutationSNPCCTTCGA-H8-A6C1-01A-11D-A32N-08TCGA-H8-A6C1-10A-01D-A32N-08g.chr8:41794801C>Tc.3325G>Ac.(3325-3327)Gaa>Aaap.E1109K
PAAD84183471841834718+Missense_MutationSNPCCGTCGA-HZ-7918-01A-11D-2154-08TCGA-HZ-7918-10A-01D-2154-08g.chr8:41834718C>Gc.1171G>Cc.(1171-1173)Gac>Cacp.D391H
PCPG84179230241792302+SilentSNPAAGTCGA-SA-A6C2-01A-11D-A35I-08TCGA-SA-A6C2-10A-01D-A35G-08g.chr8:41792302A>Gc.3436T>Cc.(3436-3438)Ttg>Ctgp.L1146L
PCPG84180539641805396+Missense_MutationSNPTTATCGA-QR-A6GT-01A-11D-A35D-08TCGA-QR-A6GT-10A-01D-A35B-08g.chr8:41805396T>Ac.1775A>Tc.(1774-1776)aAc>aTcp.N592I
PRAD84179001641790016+Missense_MutationSNPCCTTCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr8:41790016C>Tc.5722G>Ac.(5722-5724)Gcc>Accp.A1908T
PRAD84179508741795087+Splice_SiteSNPCCATCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr8:41795087C>Ac.e17-1
PRAD84180040341800403+Missense_MutationSNPAACTCGA-EJ-5504-01A-01D-1576-08TCGA-EJ-5504-10A-01D-1577-08g.chr8:41800403A>Cc.2344T>Gc.(2344-2346)Tcc>Gccp.S782A
PRAD84180144841801448+SilentSNPCCTTCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr8:41801448C>Tc.2046G>Ac.(2044-2046)ccG>ccAp.P682P
PRAD84183619041836190+Missense_MutationSNPGGATCGA-QU-A6IO-01A-11D-A31L-08TCGA-QU-A6IO-10A-01D-A31J-08g.chr8:41836190G>Ac.1013C>Tc.(1012-1014)cCa>cTap.P338L
PRAD84184506841845068+Missense_MutationSNPGGATCGA-CH-5762-01A-11D-1576-08TCGA-CH-5762-11A-01D-1576-08g.chr8:41845068G>Ac.614C>Tc.(613-615)cCa>cTap.P205L
PRAD84190590241905902+Missense_MutationSNPCCATCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr8:41905902C>Ac.594G>Tc.(592-594)aaG>aaTp.K198N
READ84179057341790573+Missense_MutationSNPTTGTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:41790573T>Gc.5165A>Cc.(5164-5166)gAa>gCap.E1722A
READ84179151641791516+Missense_MutationSNPCCTTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:41791516C>Tc.4222G>Ac.(4222-4224)Gaa>Aaap.E1408K
READ84179892641798926+Missense_MutationSNPCCATCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:41798926C>Ac.2473G>Tc.(2473-2475)Gat>Tatp.D825Y
READ84180676541806765+Missense_MutationSNPCCATCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr8:41806765C>Ac.1715G>Tc.(1714-1716)aGa>aTap.R572I
READ84183233841832338+Missense_MutationSNPTTCTCGA-DC-6681-01A-11D-1826-10TCGA-DC-6681-10A-01D-1826-10g.chr8:41832338T>Cc.1366A>Gc.(1366-1368)Aat>Gatp.N456D
READ84183481941834819+Missense_MutationSNPCCTTCGA-AG-A02N-01A-11W-A096-10TCGA-AG-A02N-11A-11W-A096-10g.chr8:41834819C>Tc.1070G>Ac.(1069-1071)cGa>cAap.R357Q
SARC84183453341834533+Missense_MutationSNPCCATCGA-QC-A7B5-01A-11D-A33E-09TCGA-QC-A7B5-11A-11D-A33H-09g.chr8:41834533C>Ac.1356G>Tc.(1354-1356)tgG>tgTp.W452C
SKCM84179031141790311+SilentSNPGGATCGA-EE-A29E-06A-11D-A197-08TCGA-EE-A29E-10A-01D-A199-08g.chr8:41790311G>Ac.5427C>Tc.(5425-5427)acC>acTp.T1809T
SKCM84179035241790352+Missense_MutationSNPGGATCGA-EE-A29M-06A-11D-A196-08TCGA-EE-A29M-10A-01D-A198-08g.chr8:41790352G>Ac.5386C>Tc.(5386-5388)Cca>Tcap.P1796S
SKCM84179036141790361+Nonsense_MutationSNPGGATCGA-EE-A29D-06A-11D-A197-08TCGA-EE-A29D-10A-01D-A199-08g.chr8:41790361G>Ac.5377C>Tc.(5377-5379)Cag>Tagp.Q1793*
SKCM84179040241790402+Missense_MutationSNPGGATCGA-EE-A2MD-06A-11D-A197-08TCGA-EE-A2MD-10A-01D-A199-08g.chr8:41790402G>Ac.5336C>Tc.(5335-5337)tCc>tTcp.S1779F
SKCM84179125641791256+SilentSNPGGATCGA-GF-A4EO-06A-12D-A24R-08TCGA-GF-A4EO-10A-01D-A24R-08g.chr8:41791256G>Ac.4482C>Tc.(4480-4482)gtC>gtTp.V1494V
SKCM84179134141791341+Missense_MutationSNPGGATCGA-RP-A694-06A-11D-A30X-08TCGA-RP-A694-10A-01D-A30X-08g.chr8:41791341G>Ac.4397C>Tc.(4396-4398)cCt>cTtp.P1466L
SKCM84179137441791374+Missense_MutationSNPGGATCGA-D3-A3C7-06A-11D-A196-08TCGA-D3-A3C7-10A-01D-A198-08g.chr8:41791374G>Ac.4364C>Tc.(4363-4365)aCc>aTcp.T1455I
SKCM84179173041791730+SilentSNPGGATCGA-DA-A1HY-06A-11D-A19A-08TCGA-DA-A1HY-10A-01D-A19A-08g.chr8:41791730G>Ac.4008C>Tc.(4006-4008)ccC>ccTp.P1336P
SKCM84179215241792152+Missense_MutationSNPGGATCGA-EE-A2ML-06A-11D-A197-08TCGA-EE-A2ML-10A-01D-A199-08g.chr8:41792152G>Ac.3586C>Tc.(3586-3588)Cct>Tctp.P1196S
SKCM84179215241792152+Missense_MutationSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr8:41792152G>Ac.3586C>Tc.(3586-3588)Cct>Tctp.P1196S
SKCM84179215741792157+Missense_MutationSNPGGATCGA-EE-A3AC-06A-11D-A196-08TCGA-EE-A3AC-10A-01D-A198-08g.chr8:41792157G>Ac.3581C>Tc.(3580-3582)tCc>tTcp.S1194F
SKCM84179230941792309+SilentSNPGGTTCGA-ER-A19F-06A-11D-A196-08TCGA-ER-A19F-10A-01D-A198-08g.chr8:41792309G>Tc.3429C>Ac.(3427-3429)tcC>tcAp.S1143S
SKCM84179867541798675+SilentSNPGGATCGA-D3-A2J7-06A-11D-A196-08TCGA-D3-A2J7-10A-01D-A198-08g.chr8:41798675G>Ac.2724C>Tc.(2722-2724)gcC>gcTp.A908A
SKCM84180131841801318+Missense_MutationSNPCCTTCGA-GN-A266-06A-11D-A197-08TCGA-GN-A266-10A-01D-A199-08g.chr8:41801318C>Tc.2176G>Ac.(2176-2178)Gac>Aacp.D726N
SKCM84180132841801328+SilentSNPGGATCGA-DA-A1HV-06A-21D-A196-08TCGA-DA-A1HV-10A-01D-A198-08g.chr8:41801328G>Ac.2166C>Tc.(2164-2166)atC>atTp.I722I
SKCM84180143841801438+Missense_MutationSNPGGCTCGA-ER-A3EV-06A-11D-A20D-08TCGA-ER-A3EV-10A-01D-A20D-08g.chr8:41801438G>Cc.2056C>Gc.(2056-2058)Ctg>Gtgp.L686V
SKCM84180678341806783+Missense_MutationSNPGGATCGA-GN-A4U8-06A-11D-A32N-08TCGA-GN-A4U8-10B-01D-A32N-08g.chr8:41806783G>Ac.1697C>Tc.(1696-1698)cCt>cTtp.P566L
SKCM84181283741812837+SilentSNPGGATCGA-D3-A2JH-06A-11D-A196-08TCGA-D3-A2JH-10A-01D-A198-08g.chr8:41812837G>Ac.1575C>Tc.(1573-1575)tcC>tcTp.S525S
SKCM84181290141812901+Missense_MutationSNPGGATCGA-EE-A29D-06A-11D-A197-08TCGA-EE-A29D-10A-01D-A199-08g.chr8:41812901G>Ac.1511C>Tc.(1510-1512)cCa>cTap.P504L
SKCM84183227641832276+SilentSNPGGATCGA-ER-A193-06A-12D-A197-08TCGA-ER-A193-10A-01D-A199-08g.chr8:41832276G>Ac.1428C>Tc.(1426-1428)atC>atTp.I476I
SKCM84183475141834751+Missense_MutationSNPCCTTCGA-GF-A6C9-06A-11D-A30X-08TCGA-GF-A6C9-10A-01D-A30X-08g.chr8:41834751C>Tc.1138G>Ac.(1138-1140)Gaa>Aaap.E380K
SKCM84183478841834788+Missense_MutationSNPTTATCGA-DA-A1I5-06A-11D-A197-08TCGA-DA-A1I5-10A-01D-A199-08g.chr8:41834788T>Ac.1101A>Tc.(1099-1101)aaA>aaTp.K367N
SKCM84183482041834820+Nonsense_MutationSNPGGATCGA-EE-A2MM-06A-11D-A196-08TCGA-EE-A2MM-10A-01D-A198-08g.chr8:41834820G>Ac.1069C>Tc.(1069-1071)Cga>Tgap.R357*
SKCM84183944841839448+Missense_MutationSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr8:41839448G>Ac.734C>Tc.(733-735)tCc>tTcp.S245F
SKCM84184499641844996+Missense_MutationSNPGGATCGA-EE-A29D-06A-11D-A197-08TCGA-EE-A29D-10A-01D-A199-08g.chr8:41844996G>Ac.686C>Tc.(685-687)tCc>tTcp.S229F
SKCM84184506441845064+SilentSNPGGATCGA-RP-A693-06A-13D-A30X-08TCGA-RP-A693-10A-01D-A30X-08g.chr8:41845064G>Ac.618C>Tc.(616-618)atC>atTp.I206I
SKCM84190628741906287+Missense_MutationSNPGGATCGA-FR-A3YO-06A-11D-A23B-08TCGA-FR-A3YO-10A-01D-A23B-08g.chr8:41906287G>Ac.209C>Tc.(208-210)tCc>tTcp.S70F
SKCM84190640341906403+SilentSNPCCTTCGA-EE-A181-06A-11D-A196-08TCGA-EE-A181-10A-01D-A198-08g.chr8:41906403C>Tc.93G>Ac.(91-93)agG>agAp.R31R
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-CN84179061741790617single base substitutionCTdownstream_gene_variant
BLCA-CN84179061741790617single base substitutionCTmissense_variantM1707I5121G>A
BLCA-US84179051741790517single base substitutionCAdownstream_gene_variant
BLCA-US84179051741790517single base substitutionCAmissense_variantA1741S5221G>T
BLCA-US84179065941790659single base substitutionTGdownstream_gene_variant
BLCA-US84179065941790659single base substitutionTGsynonymous_variantP1693P5079A>C
BLCA-US84179152541791525single base substitutionCTdownstream_gene_variant
BLCA-US84179152541791525single base substitutionCTmissense_variantE1405K4213G>A
BLCA-US84179235941792359single base substitutionGCmissense_variantL1127V3379C>G
BLCA-US84179235941792359single base substitutionGCmissense_variantL707V2119C>G
BLCA-US84179488241794882single base substitutionTCdownstream_gene_variant
BLCA-US84179488241794882single base substitutionTCmissense_variantR1082G3244A>G
BLCA-US84179488241794882single base substitutionTCmissense_variantR662G1984A>G
BLCA-US84179842041798422deletion of <=200bpCTC-downstream_gene_variant
BLCA-US84179842041798422deletion of <=200bpCTC-inframe_deletionE573
BLCA-US84179842041798422deletion of <=200bpCTC-inframe_deletionE993
BLCA-US84190630541906305single base substitutionGCdownstream_gene_variant
BLCA-US84190630541906305single base substitutionGCstop_gainedS64*191C>G
BOCA-FR84179198441791984single base substitutionCTdownstream_gene_variant
BOCA-FR84179198441791984single base substitutionCTmissense_variantA1252T3754G>A
BRCA-EU84178202041782020single base substitutionGCdownstream_gene_variant
BRCA-EU84178229841782298single base substitutionGAdownstream_gene_variant
BRCA-EU84178307141783071single base substitutionGAdownstream_gene_variant
BRCA-EU84178354441783544single base substitutionGTdownstream_gene_variant
BRCA-EU84178367241783672single base substitutionGCdownstream_gene_variant
BRCA-EU84178375841783758single base substitutionCTdownstream_gene_variant
BRCA-EU84178462141784621single base substitutionCGdownstream_gene_variant
BRCA-EU84178615841786158single base substitutionCTdownstream_gene_variant
BRCA-EU84178736841787368single base substitutionAT3_prime_UTR_variant
BRCA-EU84178736841787368single base substitutionATdownstream_gene_variant
BRCA-EU84178750041787500single base substitutionTA3_prime_UTR_variant
BRCA-EU84178750041787500single base substitutionTAdownstream_gene_variant
BRCA-EU84178797741787977single base substitutionTA3_prime_UTR_variant
BRCA-EU84178797741787977single base substitutionTAdownstream_gene_variant
BRCA-EU84178901341789013single base substitutionGC3_prime_UTR_variant
BRCA-EU84178901341789013single base substitutionGCdownstream_gene_variant
BRCA-EU84178940441789404single base substitutionCG3_prime_UTR_variant
BRCA-EU84178940441789404single base substitutionCGdownstream_gene_variant
BRCA-EU84178943241789432single base substitutionCG3_prime_UTR_variant
BRCA-EU84178943241789432single base substitutionCGdownstream_gene_variant
BRCA-EU84178955341789553insertion of <=200bp-A3_prime_UTR_variant
BRCA-EU84178955341789553insertion of <=200bp-Adownstream_gene_variant
BRCA-EU84178956841789568single base substitutionCT3_prime_UTR_variant
BRCA-EU84178956841789568single base substitutionCTdownstream_gene_variant
BRCA-EU84178965441789654single base substitutionCG3_prime_UTR_variant
BRCA-EU84178965441789654single base substitutionCGdownstream_gene_variant
BRCA-EU84178981841789818single base substitutionCTdownstream_gene_variant
BRCA-EU84178981841789818single base substitutionCTmissense_variantG1974R5920G>A
BRCA-EU84178994541789945single base substitutionCTdownstream_gene_variant
BRCA-EU84178994541789945single base substitutionCTmissense_variantM1931I5793G>A
BRCA-EU84179109941791099single base substitutionCAdownstream_gene_variant
BRCA-EU84179109941791099single base substitutionCAmissense_variantD1547Y4639G>T
BRCA-EU84179239941792399deletion of <=200bpA-intron_variant
BRCA-EU84179280541792805deletion of <=200bpT-intron_variant
BRCA-EU84179332741793327single base substitutionCTintron_variant
BRCA-EU84179451641794516single base substitutionGAintron_variant
BRCA-EU84179464441794644single base substitutionTCdownstream_gene_variant
BRCA-EU84179464441794644single base substitutionTCintron_variant
BRCA-EU84179591041795910single base substitutionGAdownstream_gene_variant
BRCA-EU84179591041795910single base substitutionGAintron_variant
BRCA-EU84179639941796399single base substitutionGCdownstream_gene_variant
BRCA-EU84179639941796399single base substitutionGCintron_variant
BRCA-EU84179708141797081single base substitutionAGdownstream_gene_variant
BRCA-EU84179708141797081single base substitutionAGintron_variant
BRCA-EU84179808641798086deletion of <=200bpA-downstream_gene_variant
BRCA-EU84179808641798086deletion of <=200bpA-intron_variant
BRCA-EU84179962641799626deletion of <=200bpA-3_prime_UTR_variant
BRCA-EU84179962641799626deletion of <=200bpA-intron_variant
BRCA-EU84180007241800072single base substitutionCT3_prime_UTR_variant
BRCA-EU84180007241800072single base substitutionCTintron_variant
BRCA-EU84180025541800255single base substitutionAC3_prime_UTR_variant
BRCA-EU84180025541800255single base substitutionACintron_variant
BRCA-EU84180046941800469single base substitutionGAmissense_variantL340F1018C>T
BRCA-EU84180046941800469single base substitutionGAmissense_variantL760F2278C>T
BRCA-EU84180047041800470single base substitutionCAmissense_variantK339N1017G>T
BRCA-EU84180047041800470single base substitutionCAmissense_variantK759N2277G>T
BRCA-EU84180082041800820single base substitutionCGintron_variant
BRCA-EU84180269541802695single base substitutionGAintron_variant
BRCA-EU84180290541802905single base substitutionCTintron_variant
BRCA-EU84180327041803270single base substitutionCTintron_variant
BRCA-EU84180346341803463single base substitutionGAintron_variant
BRCA-EU84180461041804610single base substitutionCTintron_variant
BRCA-EU84180495741804957single base substitutionGCintron_variant
BRCA-EU84180548041805491deletion of <=200bpTAGAATAATATG-intron_variant
BRCA-EU84180649641806496single base substitutionTCintron_variant
BRCA-EU84180649941806499single base substitutionTCintron_variant
BRCA-EU84180657641806576single base substitutionCTintron_variant
BRCA-EU84180704041807040single base substitutionAGintron_variant
BRCA-EU84180714641807146single base substitutionGCintron_variant
BRCA-EU84180820641808206single base substitutionGCintron_variant
BRCA-EU84180898041808980single base substitutionGAintron_variant
BRCA-EU84180977041809770single base substitutionGAintron_variant
BRCA-EU84181001741810017single base substitutionGAintron_variant
BRCA-EU84181036741810367single base substitutionGTintron_variant
BRCA-EU84181045541810455single base substitutionGCintron_variant
BRCA-EU84181183441811834single base substitutionTCintron_variant
BRCA-EU84181291041812910single base substitutionGTmissense_variantP501H1502C>A
BRCA-EU84181291041812910single base substitutionGTmissense_variantP81H242C>A
BRCA-EU84181536641815366single base substitutionTC5_prime_UTR_variant
BRCA-EU84181536641815366single base substitutionTCintron_variant
BRCA-EU84181600541816005single base substitutionAGintron_variant
BRCA-EU84181600541816005single base substitutionAGupstream_gene_variant
BRCA-EU84181778341817783single base substitutionCTintron_variant
BRCA-EU84181778341817783single base substitutionCTupstream_gene_variant
BRCA-EU84181782341817823single base substitutionCTintron_variant
BRCA-EU84181782341817823single base substitutionCTupstream_gene_variant
BRCA-EU84181811441818114single base substitutionCGintron_variant
BRCA-EU84181811441818114single base substitutionCGupstream_gene_variant
BRCA-EU84181845741818457single base substitutionATintron_variant
BRCA-EU84181845741818457single base substitutionATupstream_gene_variant
BRCA-EU84181884441818844single base substitutionTAintron_variant
BRCA-EU84181884441818844single base substitutionTAupstream_gene_variant
BRCA-EU84182042841820428single base substitutionGAintron_variant
BRCA-EU84182042841820428single base substitutionGAupstream_gene_variant
BRCA-EU84182044341820443single base substitutionCTintron_variant
BRCA-EU84182044341820443single base substitutionCTupstream_gene_variant
BRCA-EU84182047841820478single base substitutionCGintron_variant
BRCA-EU84182047841820478single base substitutionCGupstream_gene_variant
BRCA-EU84182049841820498single base substitutionGAintron_variant
BRCA-EU84182049841820498single base substitutionGAupstream_gene_variant
BRCA-EU84182058841820588single base substitutionTGintron_variant
BRCA-EU84182058841820588single base substitutionTGupstream_gene_variant
BRCA-EU84182062641820626single base substitutionGCintron_variant
BRCA-EU84182062641820626single base substitutionGCupstream_gene_variant
BRCA-EU84182350441823504single base substitutionAGintron_variant
BRCA-EU84182432741824327single base substitutionGAintron_variant
BRCA-EU84182653541826535single base substitutionCGintron_variant
BRCA-EU84182745141827451single base substitutionTCdownstream_gene_variant
BRCA-EU84182745141827451single base substitutionTCintron_variant
BRCA-EU84182779741827797single base substitutionCGdownstream_gene_variant
BRCA-EU84182779741827797single base substitutionCGintron_variant
BRCA-EU84182820641828206single base substitutionGCdownstream_gene_variant
BRCA-EU84182820641828206single base substitutionGCintron_variant
BRCA-EU84182836241828362single base substitutionTCdownstream_gene_variant
BRCA-EU84182836241828362single base substitutionTCintron_variant
BRCA-EU84183036841830368deletion of <=200bpA-downstream_gene_variant
BRCA-EU84183036841830368deletion of <=200bpA-intron_variant
BRCA-EU84183088841830888single base substitutionCTdownstream_gene_variant
BRCA-EU84183088841830888single base substitutionCTintron_variant
BRCA-EU84183180341831803deletion of <=200bpC-downstream_gene_variant
BRCA-EU84183180341831803deletion of <=200bpC-intron_variant
BRCA-EU84183215241832152single base substitutionTCdownstream_gene_variant
BRCA-EU84183215241832152single base substitutionTCexon_variant
BRCA-EU84183215241832152single base substitutionTCintron_variant
BRCA-EU84183386641833866single base substitutionACintron_variant
BRCA-EU84183410741834107insertion of <=200bp-Tintron_variant
BRCA-EU84183548241835482single base substitutionGAintron_variant
BRCA-EU84183548241835482single base substitutionGAupstream_gene_variant
BRCA-EU84183677341836773single base substitutionGAintron_variant
BRCA-EU84183677341836773single base substitutionGAupstream_gene_variant
BRCA-EU84183694141836941single base substitutionGAintron_variant
BRCA-EU84183694141836941single base substitutionGAupstream_gene_variant
BRCA-EU84183758141837581single base substitutionACintron_variant
BRCA-EU84183758141837581single base substitutionACupstream_gene_variant
BRCA-EU84183771041837710deletion of <=200bpT-intron_variant
BRCA-EU84183771041837710deletion of <=200bpT-upstream_gene_variant
BRCA-EU84183856341838563single base substitutionCTintron_variant
BRCA-EU84183856341838563single base substitutionCTupstream_gene_variant
BRCA-EU84183883641838836deletion of <=200bpA-intron_variant
BRCA-EU84183883641838836deletion of <=200bpA-upstream_gene_variant
BRCA-EU84183970341839703deletion of <=200bpA-intron_variant
BRCA-EU84183970341839703deletion of <=200bpA-upstream_gene_variant
BRCA-EU84184002741840027single base substitutionCGintron_variant
BRCA-EU84184194041841940single base substitutionTAintron_variant
BRCA-EU84184410741844107deletion of <=200bpA-intron_variant
BRCA-EU84184449341844493single base substitutionTCintron_variant
BRCA-EU84184561141845611single base substitutionCTintron_variant
BRCA-EU84184597541845975single base substitutionGAintron_variant
BRCA-EU84184604841846048single base substitutionCTintron_variant
BRCA-EU84184641241846412single base substitutionCTintron_variant
BRCA-EU84184736441847364single base substitutionGTintron_variant
BRCA-EU84184802641848026single base substitutionTGintron_variant
BRCA-EU84184829141848291single base substitutionCTintron_variant
BRCA-EU84184833741848337single base substitutionCGintron_variant
BRCA-EU84184863341848633single base substitutionCAintron_variant
BRCA-EU84184864741848647single base substitutionCAintron_variant
BRCA-EU84184873041848730single base substitutionCGintron_variant
BRCA-EU84184909341849093single base substitutionTAintron_variant
BRCA-EU84184910041849100single base substitutionCAintron_variant
BRCA-EU84184911141849111single base substitutionCAintron_variant
BRCA-EU84184972741849727single base substitutionGAintron_variant
BRCA-EU84185082041850820single base substitutionCTintron_variant
BRCA-EU84185146841851468single base substitutionGTintron_variant
BRCA-EU84185174041851740single base substitutionCTintron_variant
BRCA-EU84185377541853775single base substitutionGCintron_variant
BRCA-EU84185492841854928single base substitutionCTintron_variant
BRCA-EU84185493741854937insertion of <=200bp-Aintron_variant
BRCA-EU84185519341855193single base substitutionCGintron_variant
BRCA-EU84185553541855535single base substitutionGAintron_variant
BRCA-EU84185700541857005single base substitutionCTintron_variant
BRCA-EU84185700941857009single base substitutionCAintron_variant
BRCA-EU84185704841857048single base substitutionCTintron_variant
BRCA-EU84185708441857084single base substitutionTCintron_variant
BRCA-EU84185708541857085single base substitutionCTintron_variant
BRCA-EU84185711341857113single base substitutionCAintron_variant
BRCA-EU84185754141857541single base substitutionAGintron_variant
BRCA-EU84185860341858603single base substitutionGAintron_variant
BRCA-EU84185878041858780single base substitutionAGintron_variant
BRCA-EU84185947541859475single base substitutionCAintron_variant
BRCA-EU84186258341862583single base substitutionCGintron_variant
BRCA-EU84186282841862828single base substitutionGCintron_variant
BRCA-EU84186399641863996single base substitutionGCintron_variant
BRCA-EU84186547341865473single base substitutionCGintron_variant
BRCA-EU84186566241865662deletion of <=200bpA-intron_variant
BRCA-EU84186599441865994single base substitutionTCintron_variant
BRCA-EU84186617541866175deletion of <=200bpT-intron_variant
BRCA-EU84186647241866472deletion of <=200bpT-intron_variant
BRCA-EU84186858141868581single base substitutionCAintron_variant
BRCA-EU84186902541869025single base substitutionGAintron_variant
BRCA-EU84186915941869159single base substitutionGAintron_variant
BRCA-EU84186954541869545single base substitutionCTintron_variant
BRCA-EU84187271641872716single base substitutionCAintron_variant
BRCA-EU84187412341874123single base substitutionTCintron_variant
BRCA-EU84187416241874162single base substitutionCTintron_variant
BRCA-EU84187427741874277single base substitutionCGintron_variant
BRCA-EU84187440341874403single base substitutionCTintron_variant
BRCA-EU84187440941874409single base substitutionCAintron_variant
BRCA-EU84187442241874422insertion of <=200bp-Aintron_variant
BRCA-EU84187447041874470single base substitutionCTintron_variant
BRCA-EU84187447541874475single base substitutionTCintron_variant
BRCA-EU84187458541874585single base substitutionACintron_variant
BRCA-EU84187514441875144single base substitutionAGintron_variant
BRCA-EU84187576141875761deletion of <=200bpA-intron_variant
BRCA-EU84187582041875820single base substitutionGAintron_variant
BRCA-EU84187607041876070single base substitutionCTintron_variant
BRCA-EU84187627241876272single base substitutionCTintron_variant
BRCA-EU84187644341876443insertion of <=200bp-Aintron_variant
BRCA-EU84187646741876467deletion of <=200bpA-intron_variant
BRCA-EU84187650341876503single base substitutionAGintron_variant
BRCA-EU84187689441876894single base substitutionGTintron_variant
BRCA-EU84187830841878308single base substitutionCGintron_variant
BRCA-EU84187917241879172single base substitutionGCintron_variant
BRCA-EU84187959541879595single base substitutionGCintron_variant
BRCA-EU84187977141879771single base substitutionGCintron_variant
BRCA-EU84187979241879825multiple base substitution (>=2bp and <=200bp)AAAAAGTTACACTGTGGTAAGGTTAACAGAAATTATCintron_variant
BRCA-EU84188213741882137single base substitutionCAintron_variant
BRCA-EU84188278641882786single base substitutionGAintron_variant
BRCA-EU84188424141884241single base substitutionGTintron_variant
BRCA-EU84188426841884268insertion of <=200bp-Tintron_variant
BRCA-EU84188576241885762single base substitutionGTintron_variant
BRCA-EU84188632641886326single base substitutionTAintron_variant
BRCA-EU84188648841886488single base substitutionCGintron_variant
BRCA-EU84188759741887597single base substitutionGCintron_variant
BRCA-EU84188938741889387single base substitutionGAintron_variant
BRCA-EU84189128741891287single base substitutionGAintron_variant
BRCA-EU84189172241891722single base substitutionCTintron_variant
BRCA-EU84189227341892273single base substitutionGAintron_variant
BRCA-EU84189373541893735single base substitutionTCintron_variant
BRCA-EU84189387141893871single base substitutionGCintron_variant
BRCA-EU84189435441894354single base substitutionGTintron_variant
BRCA-EU84189491441894914single base substitutionCTintron_variant
BRCA-EU84189495541894955single base substitutionTCintron_variant
BRCA-EU84189635341896353insertion of <=200bp-Tintron_variant
BRCA-EU84189726141897261insertion of <=200bp-Tintron_variant
BRCA-EU84189746541897465single base substitutionCTintron_variant
BRCA-EU84189764741897647single base substitutionTCintron_variant
BRCA-EU84189770841897708single base substitutionATintron_variant
BRCA-EU84190020941900209single base substitutionGCintron_variant
BRCA-EU84190094441900944single base substitutionGAintron_variant
BRCA-EU84190149341901493single base substitutionTCdownstream_gene_variant
BRCA-EU84190149341901493single base substitutionTCintron_variant
BRCA-EU84190218941902189single base substitutionGAdownstream_gene_variant
BRCA-EU84190218941902189single base substitutionGAintron_variant
BRCA-EU84190567641905676single base substitutionGCdownstream_gene_variant
BRCA-EU84190567641905676single base substitutionGCintron_variant
BRCA-EU84190636541906365single base substitutionCTdownstream_gene_variant
BRCA-EU84190636541906365single base substitutionCTmissense_variantR44H131G>A
BRCA-EU84190656141906561single base substitutionCT5_prime_UTR_variant
BRCA-EU84190687441906874single base substitutionACintron_variant
BRCA-EU84190773341907733single base substitutionTCintron_variant
BRCA-EU84190916341909163single base substitutionGAintron_variant
BRCA-EU84190986841909868single base substitutionGCupstream_gene_variant
BRCA-EU84191130941911309single base substitutionGTupstream_gene_variant
BRCA-EU84191311341913113single base substitutionTCupstream_gene_variant
BRCA-EU84191363241913632deletion of <=200bpT-upstream_gene_variant
BRCA-EU84191374441913744single base substitutionTCupstream_gene_variant
BRCA-FR84178202041782020single base substitutionGCdownstream_gene_variant
BRCA-FR84178229841782298single base substitutionGAdownstream_gene_variant
BRCA-FR84179211641792116single base substitutionCTdownstream_gene_variant
BRCA-FR84179211641792116single base substitutionCTmissense_variantE1208K3622G>A
BRCA-FR84179332741793327single base substitutionCTintron_variant
BRCA-FR84180082041800820single base substitutionCGintron_variant
BRCA-FR84180153441801534single base substitutionCAintron_variant
BRCA-FR84180290541802905single base substitutionCTintron_variant
BRCA-FR84181045541810455single base substitutionGCintron_variant
BRCA-FR84181884441818844single base substitutionTAintron_variant
BRCA-FR84181884441818844single base substitutionTAupstream_gene_variant
BRCA-FR84182042841820428single base substitutionGAintron_variant
BRCA-FR84182042841820428single base substitutionGAupstream_gene_variant
BRCA-FR84182049841820498single base substitutionGAintron_variant
BRCA-FR84182049841820498single base substitutionGAupstream_gene_variant
BRCA-FR84183669641836696single base substitutionGAintron_variant
BRCA-FR84183669641836696single base substitutionGAupstream_gene_variant
BRCA-FR84185989841859898single base substitutionGAintron_variant
BRCA-FR84186954541869545single base substitutionCTintron_variant
BRCA-FR84188648841886488single base substitutionCGintron_variant
BRCA-FR84189435441894354single base substitutionGTintron_variant
BRCA-FR84189625341896253single base substitutionCAintron_variant
BRCA-FR84191374441913744single base substitutionTCupstream_gene_variant
BRCA-UK84178940441789404single base substitutionCG3_prime_UTR_variant
BRCA-UK84178940441789404single base substitutionCGdownstream_gene_variant
BRCA-UK84178943241789432single base substitutionCG3_prime_UTR_variant
BRCA-UK84178943241789432single base substitutionCGdownstream_gene_variant
BRCA-UK84178956841789568single base substitutionCT3_prime_UTR_variant
BRCA-UK84178956841789568single base substitutionCTdownstream_gene_variant
BRCA-UK84178965441789654single base substitutionCG3_prime_UTR_variant
BRCA-UK84178965441789654single base substitutionCGdownstream_gene_variant
BRCA-UK84178981841789818single base substitutionCTdownstream_gene_variant
BRCA-UK84178981841789818single base substitutionCTmissense_variantG1974R5920G>A
BRCA-UK84179591041795910single base substitutionGAdownstream_gene_variant
BRCA-UK84179591041795910single base substitutionGAintron_variant
BRCA-UK84180044541800445single base substitutionCGmissense_variantD348H1042G>C
BRCA-UK84180044541800445single base substitutionCGmissense_variantD768H2302G>C
BRCA-UK84180820641808206single base substitutionGCintron_variant
BRCA-UK84185602541856025single base substitutionGCintron_variant
BRCA-UK84188513841885138single base substitutionCGintron_variant
BRCA-UK84189770841897708single base substitutionATintron_variant
BRCA-US84179060541790605single base substitutionGAdownstream_gene_variant
BRCA-US84179060541790605single base substitutionGAsynonymous_variantF1711F5133C>T
BRCA-US84179065341790653single base substitutionAGdownstream_gene_variant
BRCA-US84179065341790653single base substitutionAGsynonymous_variantP1695P5085T>C
BRCA-US84179065941790659single base substitutionTGdownstream_gene_variant
BRCA-US84179065941790659single base substitutionTGsynonymous_variantP1693P5079A>C
BRCA-US84179183041791830single base substitutionTCdownstream_gene_variant
BRCA-US84179183041791830single base substitutionTCmissense_variantD1303G3908A>G
BRCA-US84179187141791873deletion of <=200bpCTC-downstream_gene_variant
BRCA-US84179187141791873deletion of <=200bpCTC-inframe_deletionE1289
BRCA-US84179198041791980single base substitutionGAdownstream_gene_variant
BRCA-US84179198041791980single base substitutionGAmissense_variantS1253F3758C>T
BRCA-US84179223241792232single base substitutionCTdownstream_gene_variant
BRCA-US84179223241792232single base substitutionCTmissense_variantR1169Q3506G>A
BRCA-US84179838641798386single base substitutionGTdownstream_gene_variant
BRCA-US84179838641798386single base substitutionGTmissense_variantL1005I3013C>A
BRCA-US84179838641798386single base substitutionGTmissense_variantL585I1753C>A
BRCA-US84179858841798588single base substitutionCGdownstream_gene_variant
BRCA-US84179858841798588single base substitutionCGmissense_variantK517N1551G>C
BRCA-US84179858841798588single base substitutionCGmissense_variantK937N2811G>C
BRCA-US84183458841834588single base substitutionGCexon_variant
BRCA-US84183458841834588single base substitutionGCmissense_variantS434C1301C>G
BRCA-US84190616241906162single base substitutionCGdownstream_gene_variant
BRCA-US84190616241906162single base substitutionCGmissense_variantE112Q334G>C
BTCA-JP84179064041790640single base substitutionGAdownstream_gene_variant
BTCA-JP84179064041790640single base substitutionGAmissense_variantP1700S5098C>T
BTCA-JP84179110941791109single base substitutionCTdownstream_gene_variant
BTCA-JP84179110941791109single base substitutionCTsynonymous_variantQ1543Q4629G>A
BTCA-JP84179239941792399insertion of <=200bp-Aintron_variant
BTCA-JP84180526041805260single base substitutionCAintron_variant
BTCA-JP84181284941812849single base substitutionGCsynonymous_variantT101T303C>G
BTCA-JP84181284941812849single base substitutionGCsynonymous_variantT521T1563C>G
BTCA-JP84181449441814494single base substitutionTCintron_variant
BTCA-JP84190614141906141single base substitutionTCdownstream_gene_variant
BTCA-JP84190614141906141single base substitutionTCmissense_variantK119E355A>G
CESC-US84178976641789766single base substitutionCTdownstream_gene_variant
CESC-US84178976641789766single base substitutionCTmissense_variantG1991D5972G>A
CESC-US84179074941790749single base substitutionCTdownstream_gene_variant
CESC-US84179074941790749single base substitutionCTsynonymous_variantP1663P4989G>A
CESC-US84179840741798407single base substitutionGAdownstream_gene_variant
CESC-US84179840741798407single base substitutionGAmissense_variantR578W1732C>T
CESC-US84179840741798407single base substitutionGAmissense_variantR998W2992C>T
CESC-US84179892241798922single base substitutionGCdownstream_gene_variant
CESC-US84179892241798922single base substitutionGCmissense_variantS406C1217C>G
CESC-US84179892241798922single base substitutionGCmissense_variantS826C2477C>G
CESC-US84190638641906386single base substitutionGTdownstream_gene_variant
CESC-US84190638641906386single base substitutionGTmissense_variantS37Y110C>A
CLLE-ES84181381441813814single base substitutionACintron_variant
CLLE-ES84185140841851409multiple base substitution (>=2bp and <=200bp)GGTAintron_variant
CLLE-ES84188078141880781single base substitutionGAintron_variant
CLLE-ES84189621241896212single base substitutionGAintron_variant
CLLE-ES84190026541900265single base substitutionCAintron_variant
COAD-US84179005441790054single base substitutionCTdownstream_gene_variant
COAD-US84179005441790054single base substitutionCTmissense_variantR1895H5684G>A
COAD-US84179007041790070single base substitutionCTdownstream_gene_variant
COAD-US84179007041790070single base substitutionCTmissense_variantA1890T5668G>A
COAD-US84179049341790493single base substitutionCTdownstream_gene_variant
COAD-US84179049341790493single base substitutionCTmissense_variantA1749T5245G>A
COAD-US84179065941790659insertion of <=200bp-Gdownstream_gene_variant
COAD-US84179065941790659insertion of <=200bp-Gframeshift_variantP1693P?
COAD-US84179074741790749deletion of <=200bpGGC-disruptive_inframe_deletionPP1663P
COAD-US84179074741790749deletion of <=200bpGGC-downstream_gene_variant
COAD-US84179128341791283single base substitutionGAdownstream_gene_variant
COAD-US84179128341791283single base substitutionGAsynonymous_variantS1485S4455C>T
COAD-US84179201141792011deletion of <=200bpC-downstream_gene_variant
COAD-US84179201141792011deletion of <=200bpC-frameshift_variantD1243
COAD-US84179841741798417single base substitutionCTdownstream_gene_variant
COAD-US84179841741798417single base substitutionCTsynonymous_variantP574P1722G>A
COAD-US84179841741798417single base substitutionCTsynonymous_variantP994P2982G>A
COAD-US84179848741798487single base substitutionCTdownstream_gene_variant
COAD-US84179848741798487single base substitutionCTmissense_variantR551H1652G>A
COAD-US84179848741798487single base substitutionCTmissense_variantR971H2912G>A
COAD-US84180411541804115single base substitutionCTmissense_variantD244N730G>A
COAD-US84180411541804115single base substitutionCTmissense_variantD664N1990G>A
COAD-US84181284041812840single base substitutionGAsynonymous_variantS104S312C>T
COAD-US84181284041812840single base substitutionGAsynonymous_variantS524S1572C>T
COAD-US84183616241836162single base substitutionCTsplice_region_variant
COAD-US84183616241836162single base substitutionCTupstream_gene_variant
COAD-US84190609541906095single base substitutionAGdownstream_gene_variant
COAD-US84190609541906095single base substitutionAGmissense_variantL134S401T>C
COCA-CN84178569441785694single base substitutionCTdownstream_gene_variant
COCA-CN84178771041787710single base substitutionTC3_prime_UTR_variant
COCA-CN84178771041787710single base substitutionTCdownstream_gene_variant
COCA-CN84179001641790016single base substitutionCTdownstream_gene_variant
COCA-CN84179001641790016single base substitutionCTmissense_variantA1908T5722G>A
COCA-CN84179078641790786single base substitutionGTdownstream_gene_variant
COCA-CN84179078641790786single base substitutionGTmissense_variantP1651Q4952C>A
COCA-CN84179084641790846single base substitutionCTdownstream_gene_variant
COCA-CN84179084641790846single base substitutionCTmissense_variantS1631N4892G>A
COCA-CN84179097141790971single base substitutionGAdownstream_gene_variant
COCA-CN84179097141790971single base substitutionGAsynonymous_variantY1589Y4767C>T
COCA-CN84179109341791093single base substitutionCTdownstream_gene_variant
COCA-CN84179109341791093single base substitutionCTmissense_variantG1549S4645G>A
COCA-CN84179216141792161single base substitutionCTdownstream_gene_variant
COCA-CN84179216141792161single base substitutionCTmissense_variantV1193I3577G>A
COCA-CN84179514841795148single base substitutionGAdownstream_gene_variant
COCA-CN84179514841795148single base substitutionGAintron_variant
COCA-CN84179880241798802single base substitutionCTdownstream_gene_variant
COCA-CN84179880241798802single base substitutionCTmissense_variantG446D1337G>A
COCA-CN84179880241798802single base substitutionCTmissense_variantG866D2597G>A
COCA-CN84179880841798808single base substitutionCTdownstream_gene_variant
COCA-CN84179880841798808single base substitutionCTmissense_variantR444Q1331G>A
COCA-CN84179880841798808single base substitutionCTmissense_variantR864Q2591G>A
COCA-CN84180129041801290single base substitutionCTmissense_variantR315Q944G>A
COCA-CN84180129041801290single base substitutionCTmissense_variantR735Q2204G>A
COCA-CN84180543641805436single base substitutionGTsplice_region_variant
COCA-CN84181282041812820single base substitutionTCmissense_variantY111C332A>G
COCA-CN84181282041812820single base substitutionTCmissense_variantY531C1592A>G
COCA-CN84181299641812996single base substitutionCTintron_variant
COCA-CN84181445941814459single base substitutionGTintron_variant
COCA-CN84181667341816673single base substitutionTCintron_variant
COCA-CN84181667341816673single base substitutionTCupstream_gene_variant
COCA-CN84182762141827621single base substitutionCTdownstream_gene_variant
COCA-CN84182762141827621single base substitutionCTintron_variant
COCA-CN84182762341827623single base substitutionGAdownstream_gene_variant
COCA-CN84182762341827623single base substitutionGAintron_variant
COCA-CN84183229841832298single base substitutionCTdownstream_gene_variant
COCA-CN84183229841832298single base substitutionCTexon_variant
COCA-CN84183229841832298single base substitutionCTmissense_variantR469Q1406G>A
COCA-CN84183943641839436single base substitutionGAmissense_variantT249M746C>T
COCA-CN84183943641839436single base substitutionGAupstream_gene_variant
COCA-CN84190335541903355single base substitutionTAdownstream_gene_variant
COCA-CN84190335541903355single base substitutionTAintron_variant
COCA-CN84190597941905979single base substitutionCTdownstream_gene_variant
COCA-CN84190597941905979single base substitutionCTmissense_variantA173T517G>A
EOPC-DE84178680641786806single base substitutionTCdownstream_gene_variant
EOPC-DE84187021941870219single base substitutionGAintron_variant
ESAD-UK84178258041782580single base substitutionATdownstream_gene_variant
ESAD-UK84178481141784811single base substitutionTGdownstream_gene_variant
ESAD-UK84178657441786574deletion of <=200bpA-downstream_gene_variant
ESAD-UK84178707441787074single base substitutionAG3_prime_UTR_variant
ESAD-UK84178733841787338single base substitutionTC3_prime_UTR_variant
ESAD-UK84178733841787338single base substitutionTCdownstream_gene_variant
ESAD-UK84178739541787395single base substitutionTA3_prime_UTR_variant
ESAD-UK84178739541787395single base substitutionTAdownstream_gene_variant
ESAD-UK84178988841789888single base substitutionACdownstream_gene_variant
ESAD-UK84178988841789888single base substitutionACsynonymous_variantP1950P5850T>G
ESAD-UK84179163041791630single base substitutionCTdownstream_gene_variant
ESAD-UK84179163041791630single base substitutionCTmissense_variantE1370K4108G>A
ESAD-UK84179266741792667single base substitutionTAintron_variant
ESAD-UK84179267841792678single base substitutionACintron_variant
ESAD-UK84179856941798569single base substitutionCGdownstream_gene_variant
ESAD-UK84179856941798569single base substitutionCGmissense_variantV524L1570G>C
ESAD-UK84179856941798569single base substitutionCGmissense_variantV944L2830G>C
ESAD-UK84179960641799606single base substitutionGC3_prime_UTR_variant
ESAD-UK84179960641799606single base substitutionGCintron_variant
ESAD-UK84180081541800815single base substitutionTGintron_variant
ESAD-UK84180351841803518single base substitutionATintron_variant
ESAD-UK84180767141807671single base substitutionACintron_variant
ESAD-UK84181015741810157single base substitutionTCintron_variant
ESAD-UK84181290841812908single base substitutionGAmissense_variantP502S1504C>T
ESAD-UK84181290841812908single base substitutionGAmissense_variantP82S244C>T
ESAD-UK84181300141813001single base substitutionTAintron_variant
ESAD-UK84181822441818224single base substitutionAGintron_variant
ESAD-UK84181822441818224single base substitutionAGupstream_gene_variant
ESAD-UK84181846741818467single base substitutionTAintron_variant
ESAD-UK84181846741818467single base substitutionTAupstream_gene_variant
ESAD-UK84182041341820413single base substitutionGCintron_variant
ESAD-UK84182041341820413single base substitutionGCupstream_gene_variant
ESAD-UK84182109341821093single base substitutionAGintron_variant
ESAD-UK84182501341825013single base substitutionGAintron_variant
ESAD-UK84182691641826916single base substitutionGCdownstream_gene_variant
ESAD-UK84182691641826916single base substitutionGCintron_variant
ESAD-UK84182754841827548single base substitutionCTdownstream_gene_variant
ESAD-UK84182754841827548single base substitutionCTintron_variant
ESAD-UK84183487441834874single base substitutionGAexon_variant
ESAD-UK84183487441834874single base substitutionGAintron_variant
ESAD-UK84183487441834874single base substitutionGAupstream_gene_variant
ESAD-UK84183689441836894single base substitutionTAintron_variant
ESAD-UK84183689441836894single base substitutionTAupstream_gene_variant
ESAD-UK84183703041837030single base substitutionCGintron_variant
ESAD-UK84183703041837030single base substitutionCGupstream_gene_variant
ESAD-UK84183818041838180single base substitutionGAintron_variant
ESAD-UK84183818041838180single base substitutionGAupstream_gene_variant
ESAD-UK84183844041838440single base substitutionGAsynonymous_variantN277N831C>T
ESAD-UK84183844041838440single base substitutionGAupstream_gene_variant
ESAD-UK84183854341838543deletion of <=200bpA-intron_variant
ESAD-UK84183854341838543deletion of <=200bpA-upstream_gene_variant
ESAD-UK84184348441843484single base substitutionGAintron_variant
ESAD-UK84184364941843649single base substitutionGAintron_variant
ESAD-UK84184760541847605single base substitutionGAintron_variant
ESAD-UK84185225441852254deletion of <=200bpT-intron_variant
ESAD-UK84185281041852810single base substitutionCTintron_variant
ESAD-UK84185562341855623insertion of <=200bp-ACATAACATintron_variant
ESAD-UK84186093041860930single base substitutionGAintron_variant
ESAD-UK84186566241865662insertion of <=200bp-Aintron_variant
ESAD-UK84186662841866628single base substitutionCTintron_variant
ESAD-UK84186699841866998single base substitutionACintron_variant
ESAD-UK84186843141868431single base substitutionAGintron_variant
ESAD-UK84187045141870451single base substitutionCGintron_variant
ESAD-UK84187209741872097single base substitutionACintron_variant
ESAD-UK84187209941872099single base substitutionCGintron_variant
ESAD-UK84187562541875625single base substitutionCGintron_variant
ESAD-UK84187660841876608single base substitutionCAintron_variant
ESAD-UK84187849441878494deletion of <=200bpG-intron_variant
ESAD-UK84187944741879447single base substitutionAGintron_variant
ESAD-UK84188036041880360single base substitutionTCintron_variant
ESAD-UK84188272641882726single base substitutionTGintron_variant
ESAD-UK84188548941885489insertion of <=200bp-Tintron_variant
ESAD-UK84189568541895685single base substitutionGAintron_variant
ESAD-UK84189688441896884single base substitutionCTintron_variant
ESAD-UK84189903041899030single base substitutionGAintron_variant
ESAD-UK84190419841904198single base substitutionAGdownstream_gene_variant
ESAD-UK84190419841904198single base substitutionAGintron_variant
ESAD-UK84190648441906484single base substitutionGAsynonymous_variantL4L12C>T
ESAD-UK84191277841912778single base substitutionTGupstream_gene_variant
ESAD-UK84191307141913071single base substitutionTCupstream_gene_variant
ESAD-UK84191383041913830single base substitutionCTupstream_gene_variant
ESCA-CN84183475041834750single base substitutionTGexon_variant
ESCA-CN84183475041834750single base substitutionTGmissense_variantE380A1139A>C
ESCA-CN84183475141834751single base substitutionCAexon_variant
ESCA-CN84183475141834751single base substitutionCAstop_gainedE380*1138G>T
ESCA-CN84183625041836250single base substitutionTGmissense_variantK318T953A>C
ESCA-CN84183625041836250single base substitutionTGupstream_gene_variant
KIRC-US84179180041791800single base substitutionTCdownstream_gene_variant
KIRC-US84179180041791800single base substitutionTCmissense_variantD1313G3938A>G
KIRC-US84179228941792289single base substitutionTGdownstream_gene_variant
KIRC-US84179228941792289single base substitutionTGmissense_variantK1150T3449A>C
KIRC-US84180411741804117single base substitutionAGmissense_variantI243T728T>C
KIRC-US84180411741804117single base substitutionAGmissense_variantI663T1988T>C
KIRC-US84183621841836218single base substitutionGAmissense_variantR329W985C>T
KIRC-US84183621841836218single base substitutionGAupstream_gene_variant
KIRP-US84179194241791942single base substitutionTGdownstream_gene_variant
KIRP-US84179194241791942single base substitutionTGmissense_variantK1266Q3796A>C
KIRP-US84179492841794928single base substitutionCAdownstream_gene_variant
KIRP-US84179492841794928single base substitutionCAmissense_variantE1066D3198G>T
KIRP-US84179492841794928single base substitutionCAmissense_variantE646D1938G>T
KIRP-US84179494541794945single base substitutionATdownstream_gene_variant
KIRP-US84179494541794945single base substitutionATmissense_variantL1061I3181T>A
KIRP-US84179494541794945single base substitutionATmissense_variantL641I1921T>A
KIRP-US84179842041798422deletion of <=200bpCTC-downstream_gene_variant
KIRP-US84179842041798422deletion of <=200bpCTC-inframe_deletionE573
KIRP-US84179842041798422deletion of <=200bpCTC-inframe_deletionE993
KIRP-US84183616141836161deletion of <=200bpC-frameshift_variantV348
KIRP-US84183616141836161deletion of <=200bpC-upstream_gene_variant
LAML-KR84180413741804137single base substitutionCTsynonymous_variantK236K708G>A
LAML-KR84180413741804137single base substitutionCTsynonymous_variantK656K1968G>A
LAML-KR84180517341805173single base substitutionACintron_variant
LAML-KR84186330641863306single base substitutionATintron_variant
LGG-US84179065941790659single base substitutionTGdownstream_gene_variant
LGG-US84179065941790659single base substitutionTGsynonymous_variantP1693P5079A>C
LIAD-FR84190603841906038single base substitutionCTdownstream_gene_variant
LIAD-FR84190603841906038single base substitutionCTmissense_variantR153H458G>A
LICA-CN84179062341790623single base substitutionAGdownstream_gene_variant
LICA-CN84179062341790623single base substitutionAGsynonymous_variantC1705C5115T>C
LICA-CN84179075441790754single base substitutionGAdownstream_gene_variant
LICA-CN84179075441790754single base substitutionGAmissense_variantP1662S4984C>T
LICA-CN84179075541790755single base substitutionCAdownstream_gene_variant
LICA-CN84179075541790755single base substitutionCAsynonymous_variantP1661P4983G>T
LICA-CN84179236941792369single base substitutionCTsynonymous_variantK1123K3369G>A
LICA-CN84179236941792369single base substitutionCTsynonymous_variantK703K2109G>A
LICA-CN84179868841798688single base substitutionTAdownstream_gene_variant
LICA-CN84179868841798688single base substitutionTAmissense_variantE484V1451A>T
LICA-CN84179868841798688single base substitutionTAmissense_variantE904V2711A>T
LICA-CN84190617841906178single base substitutionTAdownstream_gene_variant
LICA-CN84190617841906178single base substitutionTAsynonymous_variantA106A318A>T
LICA-FR84178820641788206single base substitutionGA3_prime_UTR_variant
LICA-FR84178820641788206single base substitutionGAdownstream_gene_variant
LICA-FR84178992741789927insertion of <=200bp-Adownstream_gene_variant
LICA-FR84178992741789927insertion of <=200bp-Aframeshift_variantH1937H?
LICA-FR84179173141791731single base substitutionGAdownstream_gene_variant
LICA-FR84179173141791731single base substitutionGAmissense_variantP1336L4007C>T
LICA-FR84179499941794999single base substitutionCAdownstream_gene_variant
LICA-FR84179499941794999single base substitutionCAstop_gainedE1043*3127G>T
LICA-FR84179499941794999single base substitutionCAstop_gainedE623*1867G>T
LICA-FR84179503941795049deletion of <=200bpGTGGTGTTTGC-downstream_gene_variant
LICA-FR84179503941795049deletion of <=200bpGTGGTGTTTGC-frameshift_variantRKHH1026
LICA-FR84179503941795049deletion of <=200bpGTGGTGTTTGC-frameshift_variantRKHH606
LICA-FR84179787641797876single base substitutionAGdownstream_gene_variant
LICA-FR84179787641797876single base substitutionAGintron_variant
LICA-FR84180401341804013single base substitutionCTintron_variant
LICA-FR84182044041820440single base substitutionTCintron_variant
LICA-FR84182044041820440single base substitutionTCupstream_gene_variant
LICA-FR84183641541836415deletion of <=200bpG-intron_variant
LICA-FR84183641541836415deletion of <=200bpG-upstream_gene_variant
LICA-FR84183941441839414single base substitutionCAsynonymous_variantR256R768G>T
LICA-FR84183941441839414single base substitutionCAupstream_gene_variant
LICA-FR84184598541845985single base substitutionTCintron_variant
LICA-FR84187237241872425deletion of <=200bpATGTAGTTACAGGTTCAGGATTACTTGAAATACTTCGGTACATGCAGTTATTAA-intron_variant
LICA-FR84187242541872425single base substitutionACintron_variant
LICA-FR84190777941907779single base substitutionTAintron_variant
LIHC-US84179142241791422single base substitutionTCdownstream_gene_variant
LIHC-US84179142241791422single base substitutionTCmissense_variantH1439R4316A>G
LIHC-US84179881341798813single base substitutionTCdownstream_gene_variant
LIHC-US84179881341798813single base substitutionTCsynonymous_variantP442P1326A>G
LIHC-US84179881341798813single base substitutionTCsynonymous_variantP862P2586A>G
LIHC-US84180681641806816single base substitutionTCmissense_variantQ135R404A>G
LIHC-US84180681641806816single base substitutionTCmissense_variantQ555R1664A>G
LIHC-US84181287441812874single base substitutionTCmissense_variantE513G1538A>G
LIHC-US84181287441812874single base substitutionTCmissense_variantE93G278A>G
LINC-JP84178837441788374single base substitutionTC3_prime_UTR_variant
LINC-JP84178837441788374single base substitutionTCdownstream_gene_variant
LINC-JP84179074141790741single base substitutionGAdownstream_gene_variant
LINC-JP84179074141790741single base substitutionGAmissense_variantP1666L4997C>T
LINC-JP84179096641790966single base substitutionCAdownstream_gene_variant
LINC-JP84179096641790966single base substitutionCAmissense_variantG1591V4772G>T
LINC-JP84179123441791234single base substitutionCTdownstream_gene_variant
LINC-JP84179123441791234single base substitutionCTmissense_variantV1502M4504G>A
LINC-JP84179194041791940single base substitutionCTdownstream_gene_variant
LINC-JP84179194041791940single base substitutionCTsynonymous_variantK1266K3798G>A
LINC-JP84179233741792337single base substitutionTCmissense_variantK1134R3401A>G
LINC-JP84179233741792337single base substitutionTCmissense_variantK714R2141A>G
LINC-JP84179879841798798single base substitutionGAdownstream_gene_variant
LINC-JP84179879841798798single base substitutionGAsynonymous_variantR447R1341C>T
LINC-JP84179879841798798single base substitutionGAsynonymous_variantR867R2601C>T
LINC-JP84179879941798799single base substitutionCAdownstream_gene_variant
LINC-JP84179879941798799single base substitutionCAmissense_variantR447L1340G>T
LINC-JP84179879941798799single base substitutionCAmissense_variantR867L2600G>T
LINC-JP84180203841802038single base substitutionTCintron_variant
LINC-JP84181172341811723single base substitutionTCintron_variant
LINC-JP84181466341814663single base substitutionGAintron_variant
LINC-JP84181466341814663single base substitutionGAsynonymous_variantY42Y126C>T
LINC-JP84182267041822670single base substitutionACintron_variant
LINC-JP84183561441835614single base substitutionTCintron_variant
LINC-JP84183561441835614single base substitutionTCupstream_gene_variant
LINC-JP84183818041838180single base substitutionGTintron_variant
LINC-JP84183818041838180single base substitutionGTupstream_gene_variant
LINC-JP84183898041838980single base substitutionTCintron_variant
LINC-JP84183898041838980single base substitutionTCupstream_gene_variant
LINC-JP84183952841839528single base substitutionTCintron_variant
LINC-JP84183952841839528single base substitutionTCupstream_gene_variant
LINC-JP84184751841847518single base substitutionGCintron_variant
LINC-JP84187229141872291single base substitutionTCintron_variant
LINC-JP84188212641882126single base substitutionTCintron_variant
LINC-JP84189507641895076single base substitutionAGintron_variant
LINC-JP84190211341902113insertion of <=200bp-Adownstream_gene_variant
LINC-JP84190211341902113insertion of <=200bp-Aintron_variant
LINC-JP84190582441905824single base substitutionTCdownstream_gene_variant
LINC-JP84190582441905824single base substitutionTCintron_variant
LIRI-JP84178419541784195single base substitutionGCdownstream_gene_variant
LIRI-JP84178770641787710deletion of <=200bpTCATT-3_prime_UTR_variant
LIRI-JP84178770641787710deletion of <=200bpTCATT-downstream_gene_variant
LIRI-JP84179134541791345single base substitutionCAdownstream_gene_variant
LIRI-JP84179134541791345single base substitutionCAmissense_variantD1465Y4393G>T
LIRI-JP84179404541794045single base substitutionGAintron_variant
LIRI-JP84179454341794543single base substitutionTAintron_variant
LIRI-JP84179494841794948single base substitutionTCdownstream_gene_variant
LIRI-JP84179494841794948single base substitutionTCmissense_variantR1060G3178A>G
LIRI-JP84179494841794948single base substitutionTCmissense_variantR640G1918A>G
LIRI-JP84179566841795668single base substitutionTCdownstream_gene_variant
LIRI-JP84179566841795668single base substitutionTCintron_variant
LIRI-JP84180061541800615single base substitutionTCintron_variant
LIRI-JP84180468341804683single base substitutionTCintron_variant
LIRI-JP84180471941804719single base substitutionACintron_variant
LIRI-JP84180602341806023single base substitutionTCintron_variant
LIRI-JP84180612141806121single base substitutionGAintron_variant
LIRI-JP84180649841806504deletion of <=200bpATAGAAA-intron_variant
LIRI-JP84180731541807315single base substitutionTCintron_variant
LIRI-JP84181007341810073single base substitutionTCintron_variant
LIRI-JP84181379041813790single base substitutionTCintron_variant
LIRI-JP84181518541815185single base substitutionAC5_prime_UTR_variant
LIRI-JP84181518541815185single base substitutionACintron_variant
LIRI-JP84181575741815757single base substitutionGA5_prime_UTR_variant
LIRI-JP84181575741815757single base substitutionGAintron_variant
LIRI-JP84182338341823383single base substitutionGAintron_variant
LIRI-JP84182338441823384single base substitutionCAintron_variant
LIRI-JP84182444441824444single base substitutionCTintron_variant
LIRI-JP84182471841824718single base substitutionAGintron_variant
LIRI-JP84182625741826257single base substitutionTCintron_variant
LIRI-JP84183191041831910single base substitutionTCdownstream_gene_variant
LIRI-JP84183191041831910single base substitutionTCexon_variant
LIRI-JP84183191041831910single base substitutionTCintron_variant
LIRI-JP84183210841832108single base substitutionCGdownstream_gene_variant
LIRI-JP84183210841832108single base substitutionCGexon_variant
LIRI-JP84183210841832108single base substitutionCGintron_variant
LIRI-JP84183392041833920single base substitutionAGintron_variant
LIRI-JP84183420841834208single base substitutionTCintron_variant
LIRI-JP84183430641834306single base substitutionTAintron_variant
LIRI-JP84183658541836585single base substitutionAGintron_variant
LIRI-JP84183658541836585single base substitutionAGupstream_gene_variant
LIRI-JP84183805141838051single base substitutionTCintron_variant
LIRI-JP84183805141838051single base substitutionTCupstream_gene_variant
LIRI-JP84184047041840470single base substitutionACintron_variant
LIRI-JP84184238841842388single base substitutionCGintron_variant
LIRI-JP84184393541843935single base substitutionTCintron_variant
LIRI-JP84184703341847033single base substitutionACintron_variant
LIRI-JP84184703941847039single base substitutionAGintron_variant
LIRI-JP84184708141847081single base substitutionAGintron_variant
LIRI-JP84184708441847084single base substitutionAGintron_variant
LIRI-JP84185031541850315single base substitutionTCintron_variant
LIRI-JP84185269241852692insertion of <=200bp-Aintron_variant
LIRI-JP84185659641856596single base substitutionTGintron_variant
LIRI-JP84185895341858953single base substitutionGAintron_variant
LIRI-JP84185977641859776single base substitutionTAintron_variant
LIRI-JP84186200741862007single base substitutionCTintron_variant
LIRI-JP84186394041863940single base substitutionTAintron_variant
LIRI-JP84186520741865207single base substitutionGAintron_variant
LIRI-JP84186640041866400single base substitutionTCintron_variant
LIRI-JP84186644941866461deletion of <=200bpAATATAAAAGATG-intron_variant
LIRI-JP84186683241866832single base substitutionTCintron_variant
LIRI-JP84186756141867561single base substitutionATintron_variant
LIRI-JP84186815041868150single base substitutionTCintron_variant
LIRI-JP84186837341868373single base substitutionACintron_variant
LIRI-JP84187133441871334single base substitutionAGintron_variant
LIRI-JP84187858541878585single base substitutionTCintron_variant
LIRI-JP84187989441879894single base substitutionACintron_variant
LIRI-JP84188002841880028single base substitutionTAintron_variant
LIRI-JP84188008741880087single base substitutionACintron_variant
LIRI-JP84188308541883085single base substitutionTCintron_variant
LIRI-JP84188696841886968single base substitutionTCintron_variant
LIRI-JP84188774441887744single base substitutionGAintron_variant
LIRI-JP84188889741888897single base substitutionTAintron_variant
LIRI-JP84188980441889804single base substitutionTCintron_variant
LIRI-JP84189330341893303single base substitutionGCintron_variant
LIRI-JP84189399841893998single base substitutionGAintron_variant
LIRI-JP84189402541894025single base substitutionGCintron_variant
LIRI-JP84189402641894026single base substitutionGAintron_variant
LIRI-JP84189422641894226single base substitutionGAintron_variant
LIRI-JP84189423741894237single base substitutionGCintron_variant
LIRI-JP84189436341894363single base substitutionTCintron_variant
LIRI-JP84189508041895080single base substitutionCTintron_variant
LIRI-JP84189514641895146single base substitutionCTintron_variant
LIRI-JP84189586241895862single base substitutionATintron_variant
LIRI-JP84190128041901280single base substitutionTCintron_variant
LIRI-JP84190567041905670single base substitutionTCdownstream_gene_variant
LIRI-JP84190567041905670single base substitutionTCintron_variant
LIRI-JP84190712141907121deletion of <=200bpC-5_prime_UTR_variant
LIRI-JP84190712141907121deletion of <=200bpC-intron_variant
LIRI-JP84190717841907178single base substitutionAC5_prime_UTR_variant
LIRI-JP84190717841907178single base substitutionACintron_variant
LIRI-JP84190722541907225single base substitutionCAintron_variant
LIRI-JP84190722541907225single base substitutionCAsplice_region_variant
LIRI-JP84190824641908246single base substitutionAGintron_variant
LIRI-JP84191163241911632single base substitutionGTupstream_gene_variant
LIRI-JP84191370541913705single base substitutionCGupstream_gene_variant
LUSC-KR84178757641787576single base substitutionTC3_prime_UTR_variant
LUSC-KR84178757641787576single base substitutionTCdownstream_gene_variant
LUSC-KR84179003941790039single base substitutionCTdownstream_gene_variant
LUSC-KR84179003941790039single base substitutionCTmissense_variantG1900E5699G>A
LUSC-KR84179784041797840single base substitutionGAdownstream_gene_variant
LUSC-KR84179784041797840single base substitutionGAintron_variant
LUSC-KR84180517341805173single base substitutionACintron_variant
LUSC-KR84181442241814422single base substitutionTAintron_variant
LUSC-KR84181510641815106single base substitutionTG5_prime_UTR_variant
LUSC-KR84181510641815106single base substitutionTGintron_variant
LUSC-KR84181511741815117single base substitutionTG5_prime_UTR_variant
LUSC-KR84181511741815117single base substitutionTGintron_variant
LUSC-KR84181742641817426single base substitutionATintron_variant
LUSC-KR84181742641817426single base substitutionATupstream_gene_variant
LUSC-KR84185088641850886single base substitutionGCintron_variant
LUSC-KR84185256141852561single base substitutionCTintron_variant
LUSC-KR84185662641856626single base substitutionTAintron_variant
LUSC-KR84185923241859232single base substitutionCAintron_variant
LUSC-KR84186550641865506single base substitutionTAintron_variant
LUSC-KR84187104141871041single base substitutionAGintron_variant
LUSC-KR84187160741871607single base substitutionAGintron_variant
LUSC-KR84187620641876206single base substitutionCTintron_variant
LUSC-KR84188490341884903single base substitutionTAintron_variant
LUSC-KR84189827941898279single base substitutionGAintron_variant
LUSC-KR84190241741902417single base substitutionGCdownstream_gene_variant
LUSC-KR84190241741902417single base substitutionGCintron_variant
LUSC-KR84190995541909955single base substitutionCTupstream_gene_variant
LUSC-KR84191242741912427single base substitutionAGupstream_gene_variant
LUSC-US84179017541790175single base substitutionTAdownstream_gene_variant
LUSC-US84179017541790175single base substitutionTAmissense_variantI1855F5563A>T
LUSC-US84179120641791206single base substitutionTAdownstream_gene_variant
LUSC-US84179120641791206single base substitutionTAmissense_variantQ1511L4532A>T
LUSC-US84179216241792162single base substitutionGAdownstream_gene_variant
LUSC-US84179216241792162single base substitutionGAsynonymous_variantI1192I3576C>T
LUSC-US84179840341798403single base substitutionGCdownstream_gene_variant
LUSC-US84179840341798403single base substitutionGCstop_gainedS579*1736C>G
LUSC-US84179840341798403single base substitutionGCstop_gainedS999*2996C>G
LUSC-US84179877041798770single base substitutionCAdownstream_gene_variant
LUSC-US84179877041798770single base substitutionCAstop_gainedE457*1369G>T
LUSC-US84179877041798770single base substitutionCAstop_gainedE877*2629G>T
LUSC-US84180048841800488single base substitutionGAsynonymous_variantI333I999C>T
LUSC-US84180048841800488single base substitutionGAsynonymous_variantI753I2259C>T
LUSC-US84180415241804152single base substitutionACsynonymous_variantP231P693T>G
LUSC-US84180415241804152single base substitutionACsynonymous_variantP651P1953T>G
LUSC-US84180687741806877single base substitutionGAmissense_variantP115S343C>T
LUSC-US84180687741806877single base substitutionGAmissense_variantP535S1603C>T
LUSC-US84183452741834527single base substitutionTAsplice_region_variant
LUSC-US84183454941834549single base substitutionGCexon_variant
LUSC-US84183454941834549single base substitutionGCstop_gainedS447*1340C>G
LUSC-US84183469941834699single base substitutionTCexon_variant
LUSC-US84183469941834699single base substitutionTCmissense_variantN397S1190A>G
LUSC-US84183478141834781single base substitutionGAexon_variant
LUSC-US84183478141834781single base substitutionGAmissense_variantL370F1108C>T
LUSC-US84183478141834781single base substitutionGAupstream_gene_variant
LUSC-US84183480241834802single base substitutionCAexon_variant
LUSC-US84183480241834802single base substitutionCAmissense_variantG363C1087G>T
LUSC-US84183480241834802single base substitutionCAupstream_gene_variant
LUSC-US84183838841838388single base substitutionGCmissense_variantP295A883C>G
LUSC-US84183838841838388single base substitutionGCupstream_gene_variant
LUSC-US84184505941845059single base substitutionAGmissense_variantI208T623T>C
MALY-DE84178643141786431single base substitutionGAdownstream_gene_variant
MALY-DE84178670841786708single base substitutionACdownstream_gene_variant
MALY-DE84179496441794964single base substitutionGAdownstream_gene_variant
MALY-DE84179496441794964single base substitutionGAsynonymous_variantS1054S3162C>T
MALY-DE84179496441794964single base substitutionGAsynonymous_variantS634S1902C>T
MALY-DE84179520041795200single base substitutionTCdownstream_gene_variant
MALY-DE84179520041795200single base substitutionTCintron_variant
MALY-DE84179929741799297single base substitutionCAdownstream_gene_variant
MALY-DE84179929741799297single base substitutionCAintron_variant
MALY-DE84179983841799838insertion of <=200bp-T3_prime_UTR_variant
MALY-DE84179983841799838insertion of <=200bp-Tintron_variant
MALY-DE84180339541803395single base substitutionACintron_variant
MALY-DE84180531341805313single base substitutionGAstop_gainedQ200*598C>T
MALY-DE84180531341805313single base substitutionGAstop_gainedQ620*1858C>T
MALY-DE84180673641806736single base substitutionTCsplice_region_variant
MALY-DE84181115841811158single base substitutionACintron_variant
MALY-DE84182217741822177single base substitutionATintron_variant
MALY-DE84182217841822178single base substitutionAGintron_variant
MALY-DE84182370641823706single base substitutionTCintron_variant
MALY-DE84182464241824642single base substitutionTGintron_variant
MALY-DE84183124641831246single base substitutionTGdownstream_gene_variant
MALY-DE84183124641831246single base substitutionTGintron_variant
MALY-DE84183192841831928insertion of <=200bp-Tdownstream_gene_variant
MALY-DE84183192841831928insertion of <=200bp-Texon_variant
MALY-DE84183192841831928insertion of <=200bp-Tintron_variant
MALY-DE84183579841835798single base substitutionTGintron_variant
MALY-DE84183579841835798single base substitutionTGupstream_gene_variant
MALY-DE84184707641847076single base substitutionGAintron_variant
MALY-DE84184707941847079single base substitutionGAintron_variant
MALY-DE84184810141848101single base substitutionAGintron_variant
MALY-DE84184861241848612single base substitutionACintron_variant
MALY-DE84184863541848635single base substitutionATintron_variant
MALY-DE84185542541855425single base substitutionCGintron_variant
MALY-DE84185569141855691single base substitutionTAintron_variant
MALY-DE84186463041864630single base substitutionATintron_variant
MALY-DE84187927341879273single base substitutionACintron_variant
MALY-DE84188000141880001single base substitutionTAintron_variant
MALY-DE84188136341881363single base substitutionTAintron_variant
MALY-DE84188318441883184single base substitutionGCintron_variant
MALY-DE84188911841889118single base substitutionTGintron_variant
MALY-DE84188912941889129single base substitutionCAintron_variant
MALY-DE84190764241907642single base substitutionTCintron_variant
MALY-DE84191077641910776single base substitutionGAupstream_gene_variant
MALY-DE84191112841911129deletion of <=200bpAT-upstream_gene_variant
MELA-AU84178246841782468single base substitutionGAdownstream_gene_variant
MELA-AU84178262341782623single base substitutionGAdownstream_gene_variant
MELA-AU84178312241783122single base substitutionGCdownstream_gene_variant
MELA-AU84178464741784647single base substitutionGAdownstream_gene_variant
MELA-AU84178493141784931single base substitutionCTdownstream_gene_variant
MELA-AU84178528841785288single base substitutionGAdownstream_gene_variant
MELA-AU84178548841785488single base substitutionGAdownstream_gene_variant
MELA-AU84178589641785896single base substitutionGAdownstream_gene_variant
MELA-AU84178617541786175single base substitutionGAdownstream_gene_variant
MELA-AU84178724241787242single base substitutionGA3_prime_UTR_variant
MELA-AU84178732241787322single base substitutionGA3_prime_UTR_variant
MELA-AU84178732241787322single base substitutionGAdownstream_gene_variant
MELA-AU84178745241787452single base substitutionCT3_prime_UTR_variant
MELA-AU84178745241787452single base substitutionCTdownstream_gene_variant
MELA-AU84178820041788200single base substitutionAG3_prime_UTR_variant
MELA-AU84178820041788200single base substitutionAGdownstream_gene_variant
MELA-AU84178868241788682single base substitutionGA3_prime_UTR_variant
MELA-AU84178868241788682single base substitutionGAdownstream_gene_variant
MELA-AU84178912041789120single base substitutionGA3_prime_UTR_variant
MELA-AU84178912041789120single base substitutionGAdownstream_gene_variant
MELA-AU84178966241789662single base substitutionTG3_prime_UTR_variant
MELA-AU84178966241789662single base substitutionTGdownstream_gene_variant
MELA-AU84178971541789715single base substitutionCT3_prime_UTR_variant
MELA-AU84178971541789715single base substitutionCTdownstream_gene_variant
MELA-AU84178985241789852single base substitutionGAdownstream_gene_variant
MELA-AU84178985241789852single base substitutionGAsynonymous_variantA1962A5886C>T
MELA-AU84179040241790402single base substitutionGAdownstream_gene_variant
MELA-AU84179040241790402single base substitutionGAmissense_variantS1779F5336C>T
MELA-AU84179077441790774single base substitutionGAdownstream_gene_variant
MELA-AU84179077441790774single base substitutionGAmissense_variantP1655L4964C>T
MELA-AU84179112841791128single base substitutionGAdownstream_gene_variant
MELA-AU84179112841791128single base substitutionGAmissense_variantS1537F4610C>T
MELA-AU84179128441791284single base substitutionGAdownstream_gene_variant
MELA-AU84179128441791284single base substitutionGAmissense_variantS1485F4454C>T
MELA-AU84179153841791539multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU84179153841791539multiple base substitution (>=2bp and <=200bp)GGAAmissense_variantS1400F4199CC>TT
MELA-AU84179176141791761single base substitutionGAdownstream_gene_variant
MELA-AU84179176141791761single base substitutionGAmissense_variantS1326F3977C>T
MELA-AU84179225641792256single base substitutionATdownstream_gene_variant
MELA-AU84179225641792256single base substitutionATmissense_variantI1161N3482T>A
MELA-AU84179376641793766single base substitutionGAintron_variant
MELA-AU84179399941793999single base substitutionCTintron_variant
MELA-AU84179403841794038single base substitutionGAintron_variant
MELA-AU84179416441794164single base substitutionGAintron_variant
MELA-AU84179432341794323single base substitutionGAintron_variant
MELA-AU84179433141794331single base substitutionTGintron_variant
MELA-AU84179437241794372single base substitutionGAintron_variant
MELA-AU84179459041794590single base substitutionGAdownstream_gene_variant
MELA-AU84179459041794590single base substitutionGAintron_variant
MELA-AU84179488641794886single base substitutionGAdownstream_gene_variant
MELA-AU84179488641794886single base substitutionGAsynonymous_variantF1080F3240C>T
MELA-AU84179488641794886single base substitutionGAsynonymous_variantF660F1980C>T
MELA-AU84179534041795340single base substitutionTGdownstream_gene_variant
MELA-AU84179534041795340single base substitutionTGintron_variant
MELA-AU84179574341795743single base substitutionCTdownstream_gene_variant
MELA-AU84179574341795743single base substitutionCTintron_variant
MELA-AU84179606941796069single base substitutionGAdownstream_gene_variant
MELA-AU84179606941796069single base substitutionGAintron_variant
MELA-AU84179613441796134single base substitutionAGdownstream_gene_variant
MELA-AU84179613441796134single base substitutionAGintron_variant
MELA-AU84179685141796851single base substitutionAGdownstream_gene_variant
MELA-AU84179685141796851single base substitutionAGintron_variant
MELA-AU84179723241797232single base substitutionGAdownstream_gene_variant
MELA-AU84179723241797232single base substitutionGAintron_variant
MELA-AU84179985541799855single base substitutionGA3_prime_UTR_variant
MELA-AU84179985541799855single base substitutionGAintron_variant
MELA-AU84180003241800032single base substitutionAT3_prime_UTR_variant
MELA-AU84180003241800032single base substitutionATintron_variant
MELA-AU84180026441800264single base substitutionAT3_prime_UTR_variant
MELA-AU84180026441800264single base substitutionATintron_variant
MELA-AU84180100441801004single base substitutionGAintron_variant
MELA-AU84180199341801993single base substitutionGAintron_variant
MELA-AU84180205741802057single base substitutionAGintron_variant
MELA-AU84180333741803337single base substitutionGAintron_variant
MELA-AU84180404941804049single base substitutionCTintron_variant
MELA-AU84180405941804059single base substitutionCGintron_variant
MELA-AU84180409641804096single base substitutionATintron_variant
MELA-AU84180424541804245single base substitutionATintron_variant
MELA-AU84180477741804777single base substitutionGAintron_variant
MELA-AU84180501641805016single base substitutionGAintron_variant
MELA-AU84180612141806121single base substitutionGAintron_variant
MELA-AU84180627641806276single base substitutionGAintron_variant
MELA-AU84180670241806702single base substitutionAGintron_variant
MELA-AU84180689041806890single base substitutionGAintron_variant
MELA-AU84180714641807146single base substitutionGAintron_variant
MELA-AU84180726841807268single base substitutionCTintron_variant
MELA-AU84180790641807906single base substitutionGAintron_variant
MELA-AU84180820041808200single base substitutionGTintron_variant
MELA-AU84180841041808410single base substitutionGAintron_variant
MELA-AU84180844341808443single base substitutionGAintron_variant
MELA-AU84180959841809598single base substitutionGAintron_variant
MELA-AU84181118341811183single base substitutionGAintron_variant
MELA-AU84181120241811202single base substitutionGAintron_variant
MELA-AU84181130541811305single base substitutionGAintron_variant
MELA-AU84181398541813985single base substitutionGAintron_variant
MELA-AU84181521141815211single base substitutionGA5_prime_UTR_variant
MELA-AU84181521141815211single base substitutionGAintron_variant
MELA-AU84181532241815322single base substitutionCT5_prime_UTR_variant
MELA-AU84181532241815322single base substitutionCTintron_variant
MELA-AU84181567241815672single base substitutionGA5_prime_UTR_variant
MELA-AU84181567241815672single base substitutionGAintron_variant
MELA-AU84181659841816598single base substitutionGAintron_variant
MELA-AU84181659841816598single base substitutionGAupstream_gene_variant
MELA-AU84181703541817035single base substitutionGAintron_variant
MELA-AU84181703541817035single base substitutionGAupstream_gene_variant
MELA-AU84181785741817857single base substitutionGAintron_variant
MELA-AU84181785741817857single base substitutionGAupstream_gene_variant
MELA-AU84181900441819004single base substitutionGAintron_variant
MELA-AU84181900441819004single base substitutionGAupstream_gene_variant
MELA-AU84181903341819033single base substitutionGAintron_variant
MELA-AU84181903341819033single base substitutionGAupstream_gene_variant
MELA-AU84181916541819165single base substitutionGAintron_variant
MELA-AU84181916541819165single base substitutionGAupstream_gene_variant
MELA-AU84181917841819178single base substitutionGAintron_variant
MELA-AU84181917841819178single base substitutionGAupstream_gene_variant
MELA-AU84181918141819181single base substitutionGAintron_variant
MELA-AU84181918141819181single base substitutionGAupstream_gene_variant
MELA-AU84181946141819461single base substitutionGAintron_variant
MELA-AU84181946141819461single base substitutionGAupstream_gene_variant
MELA-AU84182059441820594single base substitutionTCintron_variant
MELA-AU84182059441820594single base substitutionTCupstream_gene_variant
MELA-AU84182066041820660single base substitutionTAintron_variant
MELA-AU84182066041820660single base substitutionTAupstream_gene_variant
MELA-AU84182122041821220single base substitutionATintron_variant
MELA-AU84182206541822065single base substitutionGAintron_variant
MELA-AU84182262241822622single base substitutionGTintron_variant
MELA-AU84182290141822901single base substitutionGAintron_variant
MELA-AU84182336141823361single base substitutionTCintron_variant
MELA-AU84182431041824310single base substitutionGAintron_variant
MELA-AU84182447341824473single base substitutionGAintron_variant
MELA-AU84182478341824783single base substitutionATintron_variant
MELA-AU84182531241825312single base substitutionGAintron_variant
MELA-AU84182666241826662single base substitutionGAintron_variant
MELA-AU84182720241827202single base substitutionTCdownstream_gene_variant
MELA-AU84182720241827202single base substitutionTCintron_variant
MELA-AU84182727141827271single base substitutionGAdownstream_gene_variant
MELA-AU84182727141827271single base substitutionGAintron_variant
MELA-AU84182744841827448single base substitutionCTdownstream_gene_variant
MELA-AU84182744841827448single base substitutionCTintron_variant
MELA-AU84182751641827516single base substitutionAGdownstream_gene_variant
MELA-AU84182751641827516single base substitutionAGintron_variant
MELA-AU84182773341827733single base substitutionGAdownstream_gene_variant
MELA-AU84182773341827733single base substitutionGAintron_variant
MELA-AU84182779841827798single base substitutionCTdownstream_gene_variant
MELA-AU84182779841827798single base substitutionCTintron_variant
MELA-AU84182786641827866single base substitutionGAdownstream_gene_variant
MELA-AU84182786641827866single base substitutionGAintron_variant
MELA-AU84182796841827968single base substitutionCTdownstream_gene_variant
MELA-AU84182796841827968single base substitutionCTintron_variant
MELA-AU84182819341828193single base substitutionGAdownstream_gene_variant
MELA-AU84182819341828193single base substitutionGAintron_variant
MELA-AU84182845841828458single base substitutionGAdownstream_gene_variant
MELA-AU84182845841828458single base substitutionGAintron_variant
MELA-AU84182910441829104single base substitutionGAdownstream_gene_variant
MELA-AU84182910441829104single base substitutionGAintron_variant
MELA-AU84182919141829191single base substitutionGCdownstream_gene_variant
MELA-AU84182919141829191single base substitutionGCintron_variant
MELA-AU84183004441830044single base substitutionGAdownstream_gene_variant
MELA-AU84183004441830044single base substitutionGAintron_variant
MELA-AU84183020441830204single base substitutionGAdownstream_gene_variant
MELA-AU84183020441830204single base substitutionGAintron_variant
MELA-AU84183037941830379single base substitutionCTdownstream_gene_variant
MELA-AU84183037941830379single base substitutionCTintron_variant
MELA-AU84183060741830607single base substitutionATdownstream_gene_variant
MELA-AU84183060741830607single base substitutionATintron_variant
MELA-AU84183075241830752single base substitutionTCdownstream_gene_variant
MELA-AU84183075241830752single base substitutionTCintron_variant
MELA-AU84183090041830900single base substitutionGAdownstream_gene_variant
MELA-AU84183090041830900single base substitutionGAintron_variant
MELA-AU84183230241832302single base substitutionCTdownstream_gene_variant
MELA-AU84183230241832302single base substitutionCTexon_variant
MELA-AU84183230241832302single base substitutionCTmissense_variantE468K1402G>A
MELA-AU84183244541832445single base substitutionGAintron_variant
MELA-AU84183289241832892single base substitutionGAintron_variant
MELA-AU84183463341834633single base substitutionGAexon_variant
MELA-AU84183463341834633single base substitutionGAmissense_variantP419L1256C>T
MELA-AU84183482041834820single base substitutionGAexon_variant
MELA-AU84183482041834820single base substitutionGAstop_gainedR357*1069C>T
MELA-AU84183482041834820single base substitutionGAupstream_gene_variant
MELA-AU84183503841835038single base substitutionGAintron_variant
MELA-AU84183503841835038single base substitutionGAupstream_gene_variant
MELA-AU84183518341835183single base substitutionGAintron_variant
MELA-AU84183518341835183single base substitutionGAupstream_gene_variant
MELA-AU84183581841835818single base substitutionCAintron_variant
MELA-AU84183581841835818single base substitutionCAupstream_gene_variant
MELA-AU84183594741835947single base substitutionGAintron_variant
MELA-AU84183594741835947single base substitutionGAupstream_gene_variant
MELA-AU84183648141836481single base substitutionGAintron_variant
MELA-AU84183648141836481single base substitutionGAupstream_gene_variant
MELA-AU84183686341836863single base substitutionGAintron_variant
MELA-AU84183686341836863single base substitutionGAupstream_gene_variant
MELA-AU84183747841837478single base substitutionGAintron_variant
MELA-AU84183747841837478single base substitutionGAupstream_gene_variant
MELA-AU84183758541837585single base substitutionGAintron_variant
MELA-AU84183758541837585single base substitutionGAupstream_gene_variant
MELA-AU84183787041837870single base substitutionTGintron_variant
MELA-AU84183787041837870single base substitutionTGupstream_gene_variant
MELA-AU84183845241838452single base substitutionGAsplice_region_variant
MELA-AU84183845241838452single base substitutionGAupstream_gene_variant
MELA-AU84183941541839415single base substitutionCTmissense_variantR256Q767G>A
MELA-AU84183941541839415single base substitutionCTupstream_gene_variant
MELA-AU84183950041839500single base substitutionGAintron_variant
MELA-AU84183950041839500single base substitutionGAupstream_gene_variant
MELA-AU84183990041839900single base substitutionGAintron_variant
MELA-AU84183990041839900single base substitutionGAupstream_gene_variant
MELA-AU84184045941840459single base substitutionGAintron_variant
MELA-AU84184047941840479single base substitutionGAintron_variant
MELA-AU84184137041841370single base substitutionGAintron_variant
MELA-AU84184185141841851single base substitutionGAintron_variant
MELA-AU84184250541842505single base substitutionACintron_variant
MELA-AU84184256541842565single base substitutionGCintron_variant
MELA-AU84184270741842707single base substitutionTCintron_variant
MELA-AU84184275741842757single base substitutionCTintron_variant
MELA-AU84184298241842982single base substitutionACintron_variant
MELA-AU84184367041843670single base substitutionGAintron_variant
MELA-AU84184405341844053single base substitutionACintron_variant
MELA-AU84184412041844120single base substitutionGAintron_variant
MELA-AU84184427541844275single base substitutionGAintron_variant
MELA-AU84184444141844442multiple base substitution (>=2bp and <=200bp)ACTTintron_variant
MELA-AU84184460441844605multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU84184595241845952single base substitutionGAintron_variant
MELA-AU84184615541846155single base substitutionAGintron_variant
MELA-AU84184621641846253deletion of <=200bpTAAATATGACTAAGTGAACTGAAAAGATGGTGACGCTA-intron_variant
MELA-AU84184671641846716single base substitutionGAintron_variant
MELA-AU84184708141847081single base substitutionAGintron_variant
MELA-AU84184716941847169single base substitutionGAintron_variant
MELA-AU84184848941848489single base substitutionGAintron_variant
MELA-AU84184849041848490single base substitutionGAintron_variant
MELA-AU84185019241850192single base substitutionTAintron_variant
MELA-AU84185031941850319single base substitutionTAintron_variant
MELA-AU84185083741850837single base substitutionCTintron_variant
MELA-AU84185121141851211single base substitutionATintron_variant
MELA-AU84185167641851676single base substitutionAGintron_variant
MELA-AU84185214241852142single base substitutionCTintron_variant
MELA-AU84185264241852642single base substitutionGAintron_variant
MELA-AU84185347141853471single base substitutionGAintron_variant
MELA-AU84185413341854133single base substitutionGAintron_variant
MELA-AU84185444941854449single base substitutionAGintron_variant
MELA-AU84185486541854865single base substitutionAGintron_variant
MELA-AU84185487241854872single base substitutionGAintron_variant
MELA-AU84185493641854936single base substitutionGAintron_variant
MELA-AU84185553741855537single base substitutionGAintron_variant
MELA-AU84185562141855621single base substitutionTCintron_variant
MELA-AU84185590841855908single base substitutionCTintron_variant
MELA-AU84185632741856327single base substitutionCTintron_variant
MELA-AU84185656441856564single base substitutionGAintron_variant
MELA-AU84185757941857579single base substitutionGAintron_variant
MELA-AU84185784041857840single base substitutionGCintron_variant
MELA-AU84185814041858140single base substitutionTCintron_variant
MELA-AU84185864341858643single base substitutionTGintron_variant
MELA-AU84185942941859429single base substitutionCTintron_variant
MELA-AU84185973741859737single base substitutionGCintron_variant
MELA-AU84185975741859757single base substitutionGAintron_variant
MELA-AU84186015941860159single base substitutionGAintron_variant
MELA-AU84186066741860667single base substitutionGAintron_variant
MELA-AU84186133841861338single base substitutionGAintron_variant
MELA-AU84186162941861629single base substitutionGAintron_variant
MELA-AU84186345041863450single base substitutionCTintron_variant
MELA-AU84186348441863484single base substitutionGAintron_variant
MELA-AU84186362841863628single base substitutionAGintron_variant
MELA-AU84186419041864190single base substitutionGAintron_variant
MELA-AU84186433841864338single base substitutionAGintron_variant
MELA-AU84186662941866629single base substitutionGCintron_variant
MELA-AU84186726041867260single base substitutionTAintron_variant
MELA-AU84186734941867349single base substitutionCTintron_variant
MELA-AU84186735241867352single base substitutionAGintron_variant
MELA-AU84186857641868576single base substitutionCTintron_variant
MELA-AU84186864441868644single base substitutionGAintron_variant
MELA-AU84186885541868855single base substitutionGAintron_variant
MELA-AU84187097341870973single base substitutionCTintron_variant
MELA-AU84187229741872297single base substitutionAGintron_variant
MELA-AU84187293141872931single base substitutionCTintron_variant
MELA-AU84187417841874178single base substitutionGAintron_variant
MELA-AU84187491141874911single base substitutionGAintron_variant
MELA-AU84187538641875386single base substitutionGAintron_variant
MELA-AU84187642541876425single base substitutionGAintron_variant
MELA-AU84187707341877073single base substitutionGAintron_variant
MELA-AU84187722041877220single base substitutionGAintron_variant
MELA-AU84187803341878033single base substitutionTGintron_variant
MELA-AU84187814941878149single base substitutionGAintron_variant
MELA-AU84187992541879925single base substitutionGAintron_variant
MELA-AU84188006241880062single base substitutionGAintron_variant
MELA-AU84188027041880270single base substitutionATintron_variant
MELA-AU84188033241880332single base substitutionAGintron_variant
MELA-AU84188218941882189single base substitutionGAintron_variant
MELA-AU84188316941883169single base substitutionAGintron_variant
MELA-AU84188401341884013single base substitutionATintron_variant
MELA-AU84188412641884126single base substitutionGAintron_variant
MELA-AU84188437241884372single base substitutionAGintron_variant
MELA-AU84188461641884616single base substitutionGAintron_variant
MELA-AU84188515941885159single base substitutionCTintron_variant
MELA-AU84188540141885401single base substitutionAGintron_variant
MELA-AU84188636941886369single base substitutionGAintron_variant
MELA-AU84188688741886887single base substitutionGAintron_variant
MELA-AU84188708841887088single base substitutionTCintron_variant
MELA-AU84188752041887520single base substitutionGAintron_variant
MELA-AU84188754041887540single base substitutionGAintron_variant
MELA-AU84188778341887783single base substitutionGAintron_variant
MELA-AU84188816241888162single base substitutionACintron_variant
MELA-AU84188855741888557single base substitutionGAintron_variant
MELA-AU84188912841889128single base substitutionGAintron_variant
MELA-AU84188958241889582single base substitutionGAintron_variant
MELA-AU84189053241890532single base substitutionGAintron_variant
MELA-AU84189115341891154multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU84189123541891235single base substitutionTAintron_variant
MELA-AU84189139941891399single base substitutionGAintron_variant
MELA-AU84189163541891635single base substitutionGAintron_variant
MELA-AU84189417341894173single base substitutionCTintron_variant
MELA-AU84189419041894190single base substitutionGAintron_variant
MELA-AU84189438641894386single base substitutionGAintron_variant
MELA-AU84189500241895002single base substitutionGAintron_variant
MELA-AU84189517241895172single base substitutionGAintron_variant
MELA-AU84189571641895716single base substitutionGAintron_variant
MELA-AU84189584241895842deletion of <=200bpA-intron_variant
MELA-AU84189738741897387single base substitutionGAintron_variant
MELA-AU84189814541898145single base substitutionCTintron_variant
MELA-AU84189818541898186multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU84189907541899075single base substitutionGAintron_variant
MELA-AU84190000641900006single base substitutionGAintron_variant
MELA-AU84190048141900481deletion of <=200bpT-intron_variant
MELA-AU84190049641900496single base substitutionAGintron_variant
MELA-AU84190115441901154single base substitutionGAintron_variant
MELA-AU84190150541901505single base substitutionACdownstream_gene_variant
MELA-AU84190150541901505single base substitutionACintron_variant
MELA-AU84190178441901784single base substitutionGAdownstream_gene_variant
MELA-AU84190178441901784single base substitutionGAintron_variant
MELA-AU84190341841903418single base substitutionGAdownstream_gene_variant
MELA-AU84190341841903418single base substitutionGAintron_variant
MELA-AU84190403641904036single base substitutionGAdownstream_gene_variant
MELA-AU84190403641904036single base substitutionGAintron_variant
MELA-AU84190589741905897single base substitutionTAdownstream_gene_variant
MELA-AU84190589741905897single base substitutionTAmissense_variantK200M599A>T
MELA-AU84190751741907518multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU84190791141907911single base substitutionGAintron_variant
MELA-AU84190869941908699single base substitutionGCintron_variant
MELA-AU84190965741909657single base substitutionGAupstream_gene_variant
MELA-AU84191021841910218single base substitutionCTupstream_gene_variant
MELA-AU84191154741911547single base substitutionCTupstream_gene_variant
MELA-AU84191160541911605single base substitutionCTupstream_gene_variant
MELA-AU84191166841911668single base substitutionGAupstream_gene_variant
MELA-AU84191212141912121single base substitutionTAupstream_gene_variant
MELA-AU84191250641912506single base substitutionCTupstream_gene_variant
MELA-AU84191251141912511single base substitutionCTupstream_gene_variant
MELA-AU84191271941912719single base substitutionTCupstream_gene_variant
MELA-AU84191297741912977single base substitutionGAupstream_gene_variant
MELA-AU84191306341913063single base substitutionTGupstream_gene_variant
MELA-AU84191308441913084single base substitutionAGupstream_gene_variant
MELA-AU84191315341913153single base substitutionCTupstream_gene_variant
MELA-AU84191353741913537single base substitutionGAupstream_gene_variant
MELA-AU84191368441913684single base substitutionGAupstream_gene_variant
MELA-AU84191416241914162single base substitutionATupstream_gene_variant
MELA-AU84191421641914216single base substitutionCTupstream_gene_variant
MELA-AU84191434341914343single base substitutionCTupstream_gene_variant
MELA-AU84191434841914348single base substitutionCTupstream_gene_variant
MELA-AU84191436441914364single base substitutionCTupstream_gene_variant
MELA-AU84191437041914370single base substitutionGAupstream_gene_variant
MELA-AU84191441641914416single base substitutionCTupstream_gene_variant
MELA-AU84191447341914473single base substitutionGAupstream_gene_variant
ORCA-IN84179840041798400single base substitutionCAdownstream_gene_variant
ORCA-IN84179840041798400single base substitutionCAmissense_variantS1000I2999G>T
ORCA-IN84179840041798400single base substitutionCAmissense_variantS580I1739G>T
ORCA-IN84180075241800752single base substitutionCTintron_variant
ORCA-IN84180687741806877single base substitutionGAmissense_variantP115S343C>T
ORCA-IN84180687741806877single base substitutionGAmissense_variantP535S1603C>T
ORCA-IN84181874641818746single base substitutionCGintron_variant
ORCA-IN84181874641818746single base substitutionCGupstream_gene_variant
ORCA-IN84182259541822595single base substitutionTCintron_variant
ORCA-IN84187744941877449single base substitutionTGintron_variant
OV-AU84178784741787847single base substitutionCA3_prime_UTR_variant
OV-AU84178784741787847single base substitutionCAdownstream_gene_variant
OV-AU84178791541787915single base substitutionAG3_prime_UTR_variant
OV-AU84178791541787915single base substitutionAGdownstream_gene_variant
OV-AU84179631441796314single base substitutionACdownstream_gene_variant
OV-AU84179631441796314single base substitutionACintron_variant
OV-AU84180562841805628single base substitutionTCintron_variant
OV-AU84181080641810806single base substitutionGTintron_variant
OV-AU84181729041817290single base substitutionCTintron_variant
OV-AU84181729041817290single base substitutionCTupstream_gene_variant
OV-AU84182875841828758single base substitutionAGdownstream_gene_variant
OV-AU84182875841828758single base substitutionAGintron_variant
OV-AU84183345441833454single base substitutionGAintron_variant
OV-AU84183657841836578single base substitutionGAintron_variant
OV-AU84183657841836578single base substitutionGAupstream_gene_variant
OV-AU84183979341839793single base substitutionAGintron_variant
OV-AU84183979341839793single base substitutionAGupstream_gene_variant
OV-AU84184211541842115single base substitutionGCintron_variant
OV-AU84184838141848381single base substitutionCGintron_variant
OV-AU84184852541848525single base substitutionATintron_variant
OV-AU84185782441857824single base substitutionTGintron_variant
OV-AU84185965741859657single base substitutionAGintron_variant
OV-AU84186152241861522single base substitutionTAintron_variant
OV-AU84186703541867035single base substitutionCTintron_variant
OV-AU84186751141867511single base substitutionATintron_variant
OV-AU84186958641869586single base substitutionAGintron_variant
OV-AU84187056941870569single base substitutionTGintron_variant
OV-AU84187879241878792single base substitutionTGintron_variant
OV-AU84188334241883342single base substitutionCGintron_variant
OV-AU84189650941896509single base substitutionTGintron_variant
OV-AU84189712641897126single base substitutionCTintron_variant
OV-AU84190921341909213single base substitutionAGintron_variant
OV-AU84191226641912266single base substitutionCTupstream_gene_variant
PACA-AU84178735041787350single base substitutionTC3_prime_UTR_variant
PACA-AU84178735041787350single base substitutionTCdownstream_gene_variant
PACA-AU84178822841788228single base substitutionGA3_prime_UTR_variant
PACA-AU84178822841788228single base substitutionGAdownstream_gene_variant
PACA-AU84178826041788260single base substitutionTG3_prime_UTR_variant
PACA-AU84178826041788260single base substitutionTGdownstream_gene_variant
PACA-AU84180072541800725single base substitutionGAintron_variant
PACA-AU84180163241801632single base substitutionGTintron_variant
PACA-AU84180756441807564single base substitutionCGintron_variant
PACA-AU84180816441808190deletion of <=200bpTAAAGTATTTTTGTAAAAATGATAGAG-intron_variant
PACA-AU84180908841809088single base substitutionAGintron_variant
PACA-AU84181721941817219single base substitutionGTintron_variant
PACA-AU84181721941817219single base substitutionGTupstream_gene_variant
PACA-AU84182478341824783single base substitutionATintron_variant
PACA-AU84182855541828555single base substitutionCAdownstream_gene_variant
PACA-AU84182855541828555single base substitutionCAintron_variant
PACA-AU84184704641847046single base substitutionAGintron_variant
PACA-AU84184758041847580single base substitutionACintron_variant
PACA-AU84185157541851575insertion of <=200bp-Aintron_variant
PACA-AU84185317641853176single base substitutionACintron_variant
PACA-AU84185742041857420single base substitutionCAintron_variant
PACA-AU84185840841858408single base substitutionAGintron_variant
PACA-AU84185848341858483single base substitutionGAintron_variant
PACA-AU84185937941859379single base substitutionAGintron_variant
PACA-AU84186330641863306single base substitutionATintron_variant
PACA-AU84186709741867097single base substitutionTCintron_variant
PACA-AU84187097241870972single base substitutionCAintron_variant
PACA-AU84188564741885667deletion of <=200bpGTTTTAAAAAATTTGTTGAGA-intron_variant
PACA-AU84189779141897829deletion of <=200bpGAAAAAACGAGGTTAAGACCATTAGAACCTCTGGATTTC-intron_variant
PACA-AU84189892641898926single base substitutionGAintron_variant
PACA-AU84190371841903718single base substitutionATdownstream_gene_variant
PACA-AU84190371841903718single base substitutionATintron_variant
PACA-AU84190561341905613single base substitutionATdownstream_gene_variant
PACA-AU84190561341905613single base substitutionATintron_variant
PACA-AU84190642041906420single base substitutionGAdownstream_gene_variant
PACA-AU84190642041906420single base substitutionGAmissense_variantR26C76C>T
PACA-AU84190757541907578deletion of <=200bpGTAA-intron_variant
PACA-AU84191003541910035single base substitutionCAupstream_gene_variant
PACA-CA84178686141786861single base substitutionACdownstream_gene_variant
PACA-CA84178706641787066single base substitutionGA3_prime_UTR_variant
PACA-CA84178881141788811insertion of <=200bp-CAC3_prime_UTR_variant
PACA-CA84178881141788811insertion of <=200bp-CACdownstream_gene_variant
PACA-CA84178893541788935single base substitutionGA3_prime_UTR_variant
PACA-CA84178893541788935single base substitutionGAdownstream_gene_variant
PACA-CA84179239841792398insertion of <=200bp-Aintron_variant
PACA-CA84179270641792706single base substitutionTCintron_variant
PACA-CA84181462941814629single base substitutionGAintron_variant
PACA-CA84181462941814629single base substitutionGAmissense_variantR54C160C>T
PACA-CA84182042841820428single base substitutionGAintron_variant
PACA-CA84182042841820428single base substitutionGAupstream_gene_variant
PACA-CA84182077041820770single base substitutionTCintron_variant
PACA-CA84182077041820770single base substitutionTCupstream_gene_variant
PACA-CA84182362141823621single base substitutionTCintron_variant
PACA-CA84182923241829232single base substitutionCTdownstream_gene_variant
PACA-CA84182923241829232single base substitutionCTintron_variant
PACA-CA84183568441835684single base substitutionAGintron_variant
PACA-CA84183568441835684single base substitutionAGupstream_gene_variant
PACA-CA84183876841838768single base substitutionAGintron_variant
PACA-CA84183876841838768single base substitutionAGupstream_gene_variant
PACA-CA84185046441850464insertion of <=200bp-CTTintron_variant
PACA-CA84185174641851746single base substitutionCTintron_variant
PACA-CA84185527041855270single base substitutionTGintron_variant
PACA-CA84185621141856211insertion of <=200bp-TTCTATATCintron_variant
PACA-CA84187558341875583single base substitutionTCintron_variant
PACA-CA84188004841880048single base substitutionCTintron_variant
PACA-CA84188013041880130single base substitutionATintron_variant
PACA-CA84188069241880692single base substitutionTAintron_variant
PACA-CA84188206441882064single base substitutionAGintron_variant
PACA-CA84188213441882134single base substitutionTCintron_variant
PACA-CA84188373541883735single base substitutionTCintron_variant
PACA-CA84188406641884066single base substitutionGTintron_variant
PACA-CA84188704241887042single base substitutionGAintron_variant
PACA-CA84189304441893044single base substitutionGAintron_variant
PACA-CA84189458341894583single base substitutionCGintron_variant
PACA-CA84189874841898748single base substitutionAGintron_variant
PACA-CA84189876341898763single base substitutionAGintron_variant
PACA-CA84190015441900154single base substitutionGCintron_variant
PACA-CA84190101441901014deletion of <=200bpT-intron_variant
PACA-CA84190101641901016single base substitutionTCintron_variant
PACA-CA84190537041905370single base substitutionGTdownstream_gene_variant
PACA-CA84190537041905370single base substitutionGTintron_variant
PACA-CA84190672041906720single base substitutionGT5_prime_UTR_variant
PACA-CA84191368541913685single base substitutionAGupstream_gene_variant
PAEN-AU84179848741798487single base substitutionCTdownstream_gene_variant
PAEN-AU84179848741798487single base substitutionCTmissense_variantR551H1652G>A
PAEN-AU84179848741798487single base substitutionCTmissense_variantR971H2912G>A
PAEN-AU84179922141799221deletion of <=200bpA-downstream_gene_variant
PAEN-AU84179922141799221deletion of <=200bpA-intron_variant
PAEN-AU84180632741806327single base substitutionCTintron_variant
PAEN-AU84181917841819178single base substitutionGTintron_variant
PAEN-AU84181917841819178single base substitutionGTupstream_gene_variant
PAEN-AU84185455341854553single base substitutionGCintron_variant
PAEN-IT84186604941866049single base substitutionGAintron_variant
PAEN-IT84191073441910734single base substitutionTAupstream_gene_variant
PBCA-DE84178209141782091single base substitutionGAdownstream_gene_variant
PBCA-DE84180400941804009single base substitutionTCintron_variant
PBCA-DE84180859941808599single base substitutionGAintron_variant
PBCA-DE84180958441809584single base substitutionTCintron_variant
PBCA-DE84181289141812891single base substitutionGAsynonymous_variantR507R1521C>T
PBCA-DE84181289141812891single base substitutionGAsynonymous_variantR87R261C>T
PBCA-DE84182477641824776insertion of <=200bp-Tintron_variant
PBCA-DE84183789141837891single base substitutionCAintron_variant
PBCA-DE84183789141837891single base substitutionCAupstream_gene_variant
PBCA-DE84184034641840346single base substitutionAGintron_variant
PBCA-DE84184970441849704single base substitutionCTintron_variant
PBCA-DE84185095941850959single base substitutionCGintron_variant
PBCA-DE84185827941858279single base substitutionCAintron_variant
PBCA-DE84185966941859669single base substitutionAGintron_variant
PBCA-DE84186120441861204deletion of <=200bpA-intron_variant
PBCA-DE84187522441875224single base substitutionGAintron_variant
PBCA-DE84188083941880839single base substitutionCTintron_variant
PBCA-DE84188204241882042single base substitutionGTintron_variant
PBCA-DE84188920741889208deletion of <=200bpGT-intron_variant
PBCA-DE84189121941891219single base substitutionTCintron_variant
PBCA-DE84189941341899413insertion of <=200bp-Tintron_variant
PBCA-DE84190409641904096single base substitutionAGdownstream_gene_variant
PBCA-DE84190409641904096single base substitutionAGintron_variant
PBCA-DE84191429441914294single base substitutionTCupstream_gene_variant
PRAD-CA84178820041788200single base substitutionAG3_prime_UTR_variant
PRAD-CA84178820041788200single base substitutionAGdownstream_gene_variant
PRAD-CA84178820241788202single base substitutionGA3_prime_UTR_variant
PRAD-CA84178820241788202single base substitutionGAdownstream_gene_variant
PRAD-CA84178822441788224single base substitutionGA3_prime_UTR_variant
PRAD-CA84178822441788224single base substitutionGAdownstream_gene_variant
PRAD-CA84180401341804013single base substitutionCTintron_variant
PRAD-CA84181287841812878single base substitutionTCmissense_variantI512V1534A>G
PRAD-CA84181287841812878single base substitutionTCmissense_variantI92V274A>G
PRAD-CA84183222441832224single base substitutionGAdownstream_gene_variant
PRAD-CA84183222441832224single base substitutionGAexon_variant
PRAD-CA84183222441832224single base substitutionGAstop_gainedQ494*1480C>T
PRAD-CA84183941441839414single base substitutionCAsynonymous_variantR256R768G>T
PRAD-CA84183941441839414single base substitutionCAupstream_gene_variant
PRAD-CA84185272841852728single base substitutionAGintron_variant
PRAD-CA84185570641855706single base substitutionAGintron_variant
PRAD-CA84186097941860979single base substitutionGTintron_variant
PRAD-CA84186728441867284single base substitutionGCintron_variant
PRAD-CA84187064341870643single base substitutionTCintron_variant
PRAD-UK84178587641785876single base substitutionGAdownstream_gene_variant
PRAD-UK84178715741787157single base substitutionGC3_prime_UTR_variant
PRAD-UK84179949341799493single base substitutionTGdownstream_gene_variant
PRAD-UK84179949341799493single base substitutionTGintron_variant
PRAD-UK84180094041800940single base substitutionTGintron_variant
PRAD-UK84180527141805271single base substitutionTAstop_gainedK214*640A>T
PRAD-UK84180527141805271single base substitutionTAstop_gainedK634*1900A>T
PRAD-UK84180734241807342single base substitutionGAintron_variant
PRAD-UK84180938841809388single base substitutionGAintron_variant
PRAD-UK84181362341813623single base substitutionCGintron_variant
PRAD-UK84181453041814530deletion of <=200bpG-intron_variant
PRAD-UK84184098741840987single base substitutionTCintron_variant
PRAD-UK84186848841868527deletion of <=200bpTAATCAATTCAAAGAGAGAGCAGAGATAAGAGGAGATAAT-intron_variant
PRAD-UK84187261241872612single base substitutionAGintron_variant
PRAD-UK84187624641876246single base substitutionGTintron_variant
PRAD-UK84189912741899127insertion of <=200bp-CGCCTGTAATintron_variant
PRAD-UK84190714041907140single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
PRAD-UK84190714041907140single base substitutionGAintron_variant
PRAD-UK84190714041907140single base substitutionGAsplice_region_variant
PRAD-UK84190976241909762single base substitutionGAupstream_gene_variant
PRAD-UK84191268841912688single base substitutionTCupstream_gene_variant
PRAD-UK84191369341913693single base substitutionGTupstream_gene_variant
PRAD-US84180040341800403single base substitutionACmissense_variantS362A1084T>G
PRAD-US84180040341800403single base substitutionACmissense_variantS782A2344T>G
PRAD-US84183619041836190single base substitutionGAmissense_variantP338L1013C>T
PRAD-US84183619041836190single base substitutionGAupstream_gene_variant
PRAD-US84184506841845068single base substitutionGAmissense_variantP205L614C>T
READ-US84179179541791795single base substitutionCTdownstream_gene_variant
READ-US84179179541791795single base substitutionCTmissense_variantD1315N3943G>A
READ-US84179235241792352single base substitutionCTmissense_variantR1129Q3386G>A
READ-US84179235241792352single base substitutionCTmissense_variantR709Q2126G>A
READ-US84183627141836271single base substitutionCTmissense_variantR311Q932G>A
READ-US84183627141836271single base substitutionCTupstream_gene_variant
READ-US84183837541838375single base substitutionCTmissense_variantR299H896G>A
READ-US84183837541838375single base substitutionCTupstream_gene_variant
RECA-EU84178440141784401single base substitutionATdownstream_gene_variant
RECA-EU84178858741788587single base substitutionAT3_prime_UTR_variant
RECA-EU84178858741788587single base substitutionATdownstream_gene_variant
RECA-EU84179868241798682single base substitutionGAdownstream_gene_variant
RECA-EU84179868241798682single base substitutionGAmissense_variantS486L1457C>T
RECA-EU84179868241798682single base substitutionGAmissense_variantS906L2717C>T
RECA-EU84180343141803431single base substitutionCTintron_variant
RECA-EU84180965341809653single base substitutionCAintron_variant
RECA-EU84181410741814107single base substitutionTGintron_variant
RECA-EU84182790841827908single base substitutionTCdownstream_gene_variant
RECA-EU84182790841827908single base substitutionTCintron_variant
RECA-EU84182992941829929single base substitutionTGdownstream_gene_variant
RECA-EU84182992941829929single base substitutionTGintron_variant
RECA-EU84183610741836107single base substitutionAGintron_variant
RECA-EU84183610741836107single base substitutionAGupstream_gene_variant
RECA-EU84184283941842839single base substitutionAGintron_variant
RECA-EU84185588541855885single base substitutionACintron_variant
RECA-EU84186279341862793single base substitutionAGintron_variant
RECA-EU84186519241865192single base substitutionTCintron_variant
RECA-EU84187010141870101single base substitutionCTintron_variant
RECA-EU84187335641873356single base substitutionGCintron_variant
RECA-EU84187542941875429single base substitutionATintron_variant
RECA-EU84187957841879578single base substitutionAGintron_variant
RECA-EU84190476841904768single base substitutionTCdownstream_gene_variant
RECA-EU84190476841904768single base substitutionTCintron_variant
RECA-EU84190621641906216single base substitutionTCdownstream_gene_variant
RECA-EU84190621641906216single base substitutionTCmissense_variantK94E280A>G
RECA-EU84191368041913680single base substitutionAGupstream_gene_variant
SKCA-BR84178227241782272single base substitutionCAdownstream_gene_variant
SKCA-BR84178822641788226single base substitutionGA3_prime_UTR_variant
SKCA-BR84178822641788226single base substitutionGAdownstream_gene_variant
SKCA-BR84178824841788248single base substitutionTA3_prime_UTR_variant
SKCA-BR84178824841788248single base substitutionTAdownstream_gene_variant
SKCA-BR84179295641792956single base substitutionGAintron_variant
SKCA-BR84180209541802095single base substitutionGAintron_variant
SKCA-BR84180951541809515single base substitutionGAintron_variant
SKCA-BR84181034941810349single base substitutionTAintron_variant
SKCA-BR84181290241812902single base substitutionGAmissense_variantP504S1510C>T
SKCA-BR84181290241812902single base substitutionGAmissense_variantP84S250C>T
SKCA-BR84181614841816148single base substitutionAGintron_variant
SKCA-BR84181614841816148single base substitutionAGupstream_gene_variant
SKCA-BR84181693641816936single base substitutionTAintron_variant
SKCA-BR84181693641816936single base substitutionTAupstream_gene_variant
SKCA-BR84181802441818024insertion of <=200bp-CAintron_variant
SKCA-BR84181802441818024insertion of <=200bp-CAupstream_gene_variant
SKCA-BR84182214541822147deletion of <=200bpGAA-intron_variant
SKCA-BR84182479241824792insertion of <=200bp-AAATTTATTTintron_variant
SKCA-BR84182658441826584single base substitutionCTintron_variant
SKCA-BR84182658541826585single base substitutionCTintron_variant
SKCA-BR84182779841827798single base substitutionCTdownstream_gene_variant
SKCA-BR84182779841827798single base substitutionCTintron_variant
SKCA-BR84182780141827801single base substitutionGAdownstream_gene_variant
SKCA-BR84182780141827801single base substitutionGAintron_variant
SKCA-BR84182912841829129deletion of <=200bpCT-downstream_gene_variant
SKCA-BR84182912841829129deletion of <=200bpCT-intron_variant
SKCA-BR84183629541836295single base substitutionCTmissense_variantG303D908G>A
SKCA-BR84183629541836295single base substitutionCTupstream_gene_variant
SKCA-BR84183758541837585single base substitutionGAintron_variant
SKCA-BR84183758541837585single base substitutionGAupstream_gene_variant
SKCA-BR84183769641837696single base substitutionGAintron_variant
SKCA-BR84183769641837696single base substitutionGAupstream_gene_variant
SKCA-BR84184488741844887single base substitutionGAintron_variant
SKCA-BR84185077541850775single base substitutionTAintron_variant
SKCA-BR84185836041858360single base substitutionGAintron_variant
SKCA-BR84186151141861511single base substitutionGAintron_variant
SKCA-BR84186364841863648single base substitutionGAintron_variant
SKCA-BR84186494741864947single base substitutionGAintron_variant
SKCA-BR84186541241865412single base substitutionGAintron_variant
SKCA-BR84186602841866028single base substitutionAGintron_variant
SKCA-BR84186703641867036single base substitutionGAintron_variant
SKCA-BR84186743341867433single base substitutionCAintron_variant
SKCA-BR84186880641868806single base substitutionCTintron_variant
SKCA-BR84187695841876958single base substitutionGAintron_variant
SKCA-BR84187967941879679single base substitutionCAintron_variant
SKCA-BR84188855741888557single base substitutionGAintron_variant
SKCA-BR84189038541890385single base substitutionTCintron_variant
SKCA-BR84189256641892566single base substitutionGAintron_variant
SKCA-BR84189531341895313single base substitutionTAintron_variant
SKCA-BR84189727541897275single base substitutionGAintron_variant
SKCA-BR84189849241898492single base substitutionGAintron_variant
SKCA-BR84189871041898711deletion of <=200bpCA-intron_variant
SKCA-BR84189958741899587single base substitutionCGintron_variant
SKCA-BR84190198941901989single base substitutionGAdownstream_gene_variant
SKCA-BR84190198941901989single base substitutionGAintron_variant
SKCA-BR84190225041902250single base substitutionAGdownstream_gene_variant
SKCA-BR84190225041902250single base substitutionAGintron_variant
SKCA-BR84191084241910842insertion of <=200bp-ATupstream_gene_variant
SKCA-BR84191095841910958single base substitutionACupstream_gene_variant
SKCA-BR84191112741911135deletion of <=200bpGATATATAT-upstream_gene_variant
SKCA-BR84191147141911471single base substitutionCTupstream_gene_variant
SKCA-BR84191177841911778single base substitutionATupstream_gene_variant
SKCA-BR84191179541911803deletion of <=200bpATATATATG-upstream_gene_variant
SKCA-BR84191374541913745single base substitutionCTupstream_gene_variant
SKCM-US84179031141790311single base substitutionGAdownstream_gene_variant
SKCM-US84179031141790311single base substitutionGAsynonymous_variantT1809T5427C>T
SKCM-US84179035241790352single base substitutionGAdownstream_gene_variant
SKCM-US84179035241790352single base substitutionGAmissense_variantP1796S5386C>T
SKCM-US84179036141790361single base substitutionGAdownstream_gene_variant
SKCM-US84179036141790361single base substitutionGAstop_gainedQ1793*5377C>T
SKCM-US84179040241790402single base substitutionGAdownstream_gene_variant
SKCM-US84179040241790402single base substitutionGAmissense_variantS1779F5336C>T
SKCM-US84179065941790659single base substitutionTGdownstream_gene_variant
SKCM-US84179065941790659single base substitutionTGsynonymous_variantP1693P5079A>C
SKCM-US84179125641791256single base substitutionGAdownstream_gene_variant
SKCM-US84179125641791256single base substitutionGAsynonymous_variantV1494V4482C>T
SKCM-US84179134141791341single base substitutionGAdownstream_gene_variant
SKCM-US84179134141791341single base substitutionGAmissense_variantP1466L4397C>T
SKCM-US84179137441791374single base substitutionGAdownstream_gene_variant
SKCM-US84179137441791374single base substitutionGAmissense_variantT1455I4364C>T
SKCM-US84179173041791730single base substitutionGAdownstream_gene_variant
SKCM-US84179173041791730single base substitutionGAsynonymous_variantP1336P4008C>T
SKCM-US84179198241791982single base substitutionGAdownstream_gene_variant
SKCM-US84179198241791982single base substitutionGAsynonymous_variantA1252A3756C>T
SKCM-US84179215241792152single base substitutionGAdownstream_gene_variant
SKCM-US84179215241792152single base substitutionGAmissense_variantP1196S3586C>T
SKCM-US84179215741792157single base substitutionGAdownstream_gene_variant
SKCM-US84179215741792157single base substitutionGAmissense_variantS1194F3581C>T
SKCM-US84179230941792309single base substitutionGTsynonymous_variantS1143S3429C>A
SKCM-US84179230941792309single base substitutionGTsynonymous_variantS723S2169C>A
SKCM-US84179854641798546single base substitutionGCdownstream_gene_variant
SKCM-US84179854641798546single base substitutionGCsynonymous_variantL531L1593C>G
SKCM-US84179854641798546single base substitutionGCsynonymous_variantL951L2853C>G
SKCM-US84179867541798675single base substitutionGAdownstream_gene_variant
SKCM-US84179867541798675single base substitutionGAsynonymous_variantA488A1464C>T
SKCM-US84179867541798675single base substitutionGAsynonymous_variantA908A2724C>T
SKCM-US84180131841801318single base substitutionCTmissense_variantD306N916G>A
SKCM-US84180131841801318single base substitutionCTmissense_variantD726N2176G>A
SKCM-US84180132841801328single base substitutionGAsynonymous_variantI302I906C>T
SKCM-US84180132841801328single base substitutionGAsynonymous_variantI722I2166C>T
SKCM-US84180143841801438single base substitutionGCmissense_variantL266V796C>G
SKCM-US84180143841801438single base substitutionGCmissense_variantL686V2056C>G
SKCM-US84181283741812837single base substitutionGAsynonymous_variantS105S315C>T
SKCM-US84181283741812837single base substitutionGAsynonymous_variantS525S1575C>T
SKCM-US84181290141812901single base substitutionGAmissense_variantP504L1511C>T
SKCM-US84181290141812901single base substitutionGAmissense_variantP84L251C>T
SKCM-US84183224841832248single base substitutionGAdownstream_gene_variant
SKCM-US84183224841832248single base substitutionGAexon_variant
SKCM-US84183224841832248single base substitutionGAmissense_variantR486C1456C>T
SKCM-US84183227641832276single base substitutionGAdownstream_gene_variant
SKCM-US84183227641832276single base substitutionGAexon_variant
SKCM-US84183227641832276single base substitutionGAsynonymous_variantI476I1428C>T
SKCM-US84183229341832293single base substitutionAGdownstream_gene_variant
SKCM-US84183229341832293single base substitutionAGexon_variant
SKCM-US84183229341832293single base substitutionAGmissense_variantF471L1411T>C
SKCM-US84183475141834751single base substitutionCTexon_variant
SKCM-US84183475141834751single base substitutionCTmissense_variantE380K1138G>A
SKCM-US84183478841834788single base substitutionTAexon_variant
SKCM-US84183478841834788single base substitutionTAmissense_variantK367N1101A>T
SKCM-US84183478841834788single base substitutionTAupstream_gene_variant
SKCM-US84183482041834820single base substitutionGAexon_variant
SKCM-US84183482041834820single base substitutionGAstop_gainedR357*1069C>T
SKCM-US84183482041834820single base substitutionGAupstream_gene_variant
SKCM-US84183944841839448single base substitutionGAmissense_variantS245F734C>T
SKCM-US84183944841839448single base substitutionGAupstream_gene_variant
SKCM-US84184499641844996single base substitutionGAmissense_variantS229F686C>T
SKCM-US84184506441845064single base substitutionGAsynonymous_variantI206I618C>T
SKCM-US84190628741906287single base substitutionGAdownstream_gene_variant
SKCM-US84190628741906287single base substitutionGAmissense_variantS70F209C>T
SKCM-US84190640341906403single base substitutionCTdownstream_gene_variant
SKCM-US84190640341906403single base substitutionCTsynonymous_variantR31R93G>A
STAD-US84178999641789996single base substitutionCTdownstream_gene_variant
STAD-US84178999641789996single base substitutionCTmissense_variantM1914I5742G>A
STAD-US84179012841790128single base substitutionGCdownstream_gene_variant
STAD-US84179012841790128single base substitutionGCmissense_variantH1870Q5610C>G
STAD-US84179016641790166single base substitutionGAdownstream_gene_variant
STAD-US84179016641790166single base substitutionGAmissense_variantR1858C5572C>T
STAD-US84179028541790285single base substitutionGAdownstream_gene_variant
STAD-US84179028541790285single base substitutionGAmissense_variantS1818F5453C>T
STAD-US84179054941790549single base substitutionCAdownstream_gene_variant
STAD-US84179054941790549single base substitutionCAmissense_variantS1730I5189G>T
STAD-US84179065941790659single base substitutionTGdownstream_gene_variant
STAD-US84179065941790659single base substitutionTGsynonymous_variantP1693P5079A>C
STAD-US84179099641790996single base substitutionCTdownstream_gene_variant
STAD-US84179099641790996single base substitutionCTmissense_variantS1581N4742G>A
STAD-US84179102941791029single base substitutionTAdownstream_gene_variant
STAD-US84179102941791029single base substitutionTAmissense_variantD1570V4709A>T
STAD-US84179137141791371single base substitutionAGdownstream_gene_variant
STAD-US84179137141791371single base substitutionAGmissense_variantL1456P4367T>C
STAD-US84179141541791415single base substitutionGAdownstream_gene_variant
STAD-US84179141541791415single base substitutionGAsynonymous_variantG1441G4323C>T
STAD-US84179207741792077single base substitutionCTdownstream_gene_variant
STAD-US84179207741792077single base substitutionCTmissense_variantE1221K3661G>A
STAD-US84179221041792210single base substitutionATdownstream_gene_variant
STAD-US84179221041792210single base substitutionATmissense_variantS1176R3528T>A
STAD-US84179488241794882single base substitutionTGdownstream_gene_variant
STAD-US84179488241794882single base substitutionTGsynonymous_variantR1082R3244A>C
STAD-US84179488241794882single base substitutionTGsynonymous_variantR662R1984A>C
STAD-US84179492541794925single base substitutionGAdownstream_gene_variant
STAD-US84179492541794925single base substitutionGAsynonymous_variantI1067I3201C>T
STAD-US84179492541794925single base substitutionGAsynonymous_variantI647I1941C>T
STAD-US84179836441798364single base substitutionCTdownstream_gene_variant
STAD-US84179836441798364single base substitutionCTmissense_variantR1012Q3035G>A
STAD-US84179836441798364single base substitutionCTmissense_variantR592Q1775G>A
STAD-US84179853641798536single base substitutionGTdownstream_gene_variant
STAD-US84179853641798536single base substitutionGTmissense_variantP535T1603C>A
STAD-US84179853641798536single base substitutionGTmissense_variantP955T2863C>A
STAD-US84179855641798556single base substitutionCTdownstream_gene_variant
STAD-US84179855641798556single base substitutionCTmissense_variantR528Q1583G>A
STAD-US84179855641798556single base substitutionCTmissense_variantR948Q2843G>A
STAD-US84179885341798853single base substitutionTCdownstream_gene_variant
STAD-US84179885341798853single base substitutionTCmissense_variantQ429R1286A>G
STAD-US84179885341798853single base substitutionTCmissense_variantQ849R2546A>G
STAD-US84180034641800346single base substitutionCGmissense_variantE381Q1141G>C
STAD-US84180034641800346single base substitutionCGmissense_variantE801Q2401G>C
STAD-US84180040241800402single base substitutionGAmissense_variantS362F1085C>T
STAD-US84180040241800402single base substitutionGAmissense_variantS782F2345C>T
STAD-US84180138041801380single base substitutionTGmissense_variantH285P854A>C
STAD-US84180138041801380single base substitutionTGmissense_variantH705P2114A>C
STAD-US84183224841832248single base substitutionGAdownstream_gene_variant
STAD-US84183224841832248single base substitutionGAexon_variant
STAD-US84183224841832248single base substitutionGAmissense_variantR486C1456C>T
STAD-US84183461041834610single base substitutionGAexon_variant
STAD-US84183461041834610single base substitutionGAmissense_variantR427W1279C>T
STAD-US84183475841834758single base substitutionTCexon_variant
STAD-US84183475841834758single base substitutionTCsynonymous_variantS377S1131A>G
STAD-US84183476641834766single base substitutionCAexon_variant
STAD-US84183476641834766single base substitutionCAmissense_variantA375S1123G>T
STAD-US84183476641834766single base substitutionCAupstream_gene_variant
STAD-US84183620941836209single base substitutionTCmissense_variantT332A994A>G
STAD-US84183620941836209single base substitutionTCupstream_gene_variant
STAD-US84183621741836217single base substitutionCTmissense_variantR329Q986G>A
STAD-US84183621741836217single base substitutionCTupstream_gene_variant
STAD-US84183627141836271single base substitutionCTmissense_variantR311Q932G>A
STAD-US84183627141836271single base substitutionCTupstream_gene_variant
STAD-US84183943141839431single base substitutionGAstop_gainedR251*751C>T
STAD-US84183943141839431single base substitutionGAupstream_gene_variant
STAD-US84190606841906068single base substitutionACdownstream_gene_variant
STAD-US84190606841906068single base substitutionACmissense_variantF143C428T>G
STAD-US84190609141906091single base substitutionGTdownstream_gene_variant
STAD-US84190609141906091single base substitutionGTmissense_variantF135L405C>A
STAD-US84190616541906165single base substitutionCAdownstream_gene_variant
STAD-US84190616541906165single base substitutionCAmissense_variantA111S331G>T
STAD-US84190648341906483single base substitutionCTmissense_variantA5T13G>A
THCA-SA84178823041788230single base substitutionAG3_prime_UTR_variant
THCA-SA84178823041788230single base substitutionAGdownstream_gene_variant
THCA-SA84179128341791283single base substitutionGAdownstream_gene_variant
THCA-SA84179128341791283single base substitutionGAsynonymous_variantS1485S4455C>T
THCA-SA84179841741798417single base substitutionCTdownstream_gene_variant
THCA-SA84179841741798417single base substitutionCTsynonymous_variantP574P1722G>A
THCA-SA84179841741798417single base substitutionCTsynonymous_variantP994P2982G>A
THCA-SA84183454741834547single base substitutionTCexon_variant
THCA-SA84183454741834547single base substitutionTCmissense_variantS448G1342A>G
THCA-SA84190609541906095single base substitutionAGdownstream_gene_variant
THCA-SA84190609541906095single base substitutionAGmissense_variantL134S401T>C
THCA-SA84190656241906562single base substitutionAT5_prime_UTR_variant
THCA-SA84190657041906570single base substitutionCG5_prime_UTR_variant
UCEC-US84178975641789756single base substitutionCTdownstream_gene_variant
UCEC-US84178975641789756single base substitutionCTsynonymous_variantK1994K5982G>A
UCEC-US84178999141789991single base substitutionAGdownstream_gene_variant
UCEC-US84178999141789991single base substitutionAGmissense_variantM1916T5747T>C
UCEC-US84179020841790208single base substitutionTGdownstream_gene_variant
UCEC-US84179020841790208single base substitutionTGsynonymous_variantR1844R5530A>C
UCEC-US84179026441790264single base substitutionGAdownstream_gene_variant
UCEC-US84179026441790264single base substitutionGAmissense_variantS1825F5474C>T
UCEC-US84179030541790305single base substitutionCTdownstream_gene_variant
UCEC-US84179030541790305single base substitutionCTsynonymous_variantT1811T5433G>A
UCEC-US84179036841790368single base substitutionTGdownstream_gene_variant
UCEC-US84179036841790368single base substitutionTGsynonymous_variantG1790G5370A>C
UCEC-US84179038741790387single base substitutionAGdownstream_gene_variant
UCEC-US84179038741790387single base substitutionAGmissense_variantV1784A5351T>C
UCEC-US84179051241790512single base substitutionGAdownstream_gene_variant
UCEC-US84179051241790512single base substitutionGAsynonymous_variantG1742G5226C>T
UCEC-US84179063541790635single base substitutionCTdownstream_gene_variant
UCEC-US84179063541790635single base substitutionCTsynonymous_variantP1701P5103G>A
UCEC-US84179063641790636single base substitutionGAdownstream_gene_variant
UCEC-US84179063641790636single base substitutionGAmissense_variantP1701L5102C>T
UCEC-US84179068941790689single base substitutionCTdownstream_gene_variant
UCEC-US84179068941790689single base substitutionCTsynonymous_variantP1683P5049G>A
UCEC-US84179103041791030single base substitutionCTdownstream_gene_variant
UCEC-US84179103041791030single base substitutionCTmissense_variantD1570N4708G>A
UCEC-US84179103141791031single base substitutionGAdownstream_gene_variant
UCEC-US84179103141791031single base substitutionGAsynonymous_variantY1569Y4707C>T
UCEC-US84179108741791087single base substitutionTCdownstream_gene_variant
UCEC-US84179108741791087single base substitutionTCmissense_variantS1551G4651A>G
UCEC-US84179126541791265single base substitutionGAdownstream_gene_variant
UCEC-US84179126541791265single base substitutionGAsynonymous_variantS1491S4473C>T
UCEC-US84179129641791296single base substitutionCTdownstream_gene_variant
UCEC-US84179129641791296single base substitutionCTmissense_variantS1481N4442G>A
UCEC-US84179151641791516single base substitutionCTdownstream_gene_variant
UCEC-US84179151641791516single base substitutionCTmissense_variantE1408K4222G>A
UCEC-US84179154641791546single base substitutionCTdownstream_gene_variant
UCEC-US84179154641791546single base substitutionCTmissense_variantE1398K4192G>A
UCEC-US84179154941791549single base substitutionCTdownstream_gene_variant
UCEC-US84179154941791549single base substitutionCTmissense_variantE1397K4189G>A
UCEC-US84179235241792352single base substitutionCTmissense_variantR1129Q3386G>A
UCEC-US84179235241792352single base substitutionCTmissense_variantR709Q2126G>A
UCEC-US84179485641794856single base substitutionCTdownstream_gene_variant
UCEC-US84179485641794856single base substitutionCTsynonymous_variantS1090S3270G>A
UCEC-US84179485641794856single base substitutionCTsynonymous_variantS670S2010G>A
UCEC-US84179492541794925single base substitutionGAdownstream_gene_variant
UCEC-US84179492541794925single base substitutionGAsynonymous_variantI1067I3201C>T
UCEC-US84179492541794925single base substitutionGAsynonymous_variantI647I1941C>T
UCEC-US84179500441795004single base substitutionGAdownstream_gene_variant
UCEC-US84179500441795004single base substitutionGAmissense_variantT1041I3122C>T
UCEC-US84179500441795004single base substitutionGAmissense_variantT621I1862C>T
UCEC-US84179855641798556single base substitutionCTdownstream_gene_variant
UCEC-US84179855641798556single base substitutionCTmissense_variantR528Q1583G>A
UCEC-US84179855641798556single base substitutionCTmissense_variantR948Q2843G>A
UCEC-US84179856641798566single base substitutionCTdownstream_gene_variant
UCEC-US84179856641798566single base substitutionCTmissense_variantE525K1573G>A
UCEC-US84179856641798566single base substitutionCTmissense_variantE945K2833G>A
UCEC-US84179862941798629single base substitutionCTdownstream_gene_variant
UCEC-US84179862941798629single base substitutionCTmissense_variantE504K1510G>A
UCEC-US84179862941798629single base substitutionCTmissense_variantE924K2770G>A
UCEC-US84179875241798752single base substitutionCAdownstream_gene_variant
UCEC-US84179875241798752single base substitutionCAmissense_variantD463Y1387G>T
UCEC-US84179875241798752single base substitutionCAmissense_variantD883Y2647G>T
UCEC-US84180034941800349single base substitutionCTmissense_variantE380K1138G>A
UCEC-US84180034941800349single base substitutionCTmissense_variantE800K2398G>A
UCEC-US84180135041801350single base substitutionTGmissense_variantK295T884A>C
UCEC-US84180135041801350single base substitutionTGmissense_variantK715T2144A>C
UCEC-US84180686541806865single base substitutionGAmissense_variantL119F355C>T
UCEC-US84180686541806865single base substitutionGAmissense_variantL539F1615C>T
UCEC-US84183222041832220single base substitutionAGdownstream_gene_variant
UCEC-US84183222041832220single base substitutionAGexon_variant
UCEC-US84183222041832220single base substitutionAGsplice_donor_variant
UCEC-US84183226741832267single base substitutionCAdownstream_gene_variant
UCEC-US84183226741832267single base substitutionCAexon_variant
UCEC-US84183226741832267single base substitutionCAmissense_variantE479D1437G>T
UCEC-US84183470641834706single base substitutionCAexon_variant
UCEC-US84183470641834706single base substitutionCAmissense_variantD395Y1183G>T
UCEC-US84183479541834795single base substitutionTGexon_variant
UCEC-US84183479541834795single base substitutionTGmissense_variantK365T1094A>C
UCEC-US84183479541834795single base substitutionTGupstream_gene_variant
UCEC-US84183839541838395single base substitutionAGsynonymous_variantC292C876T>C
UCEC-US84183839541838395single base substitutionAGupstream_gene_variant
UCEC-US84183935841839358single base substitutionGAmissense_variantA275V824C>T
UCEC-US84183935841839358single base substitutionGAupstream_gene_variant
UCEC-US84190649241906492single base substitutionCTmissense_variantV2I4G>A
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
Pat_65_ACOSM5874705c.3415delGp.E1139fs*8Deletion - Frameshift8:41934805-41934805-
TCGA-D1-A0ZO-01COSM1099907c.5102C>Tp.P1701LSubstitution - Missense8:41933118-41933118-
TCGA-CD-A4MG-01COSM3900235c.5453C>Tp.S1818FSubstitution - Missense8:41932767-41932767-
sysucc-325TCOSM5461311c.4645G>Ap.G1549SSubstitution - Missense8:41933575-41933575-
T3610COSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
CLL152COSM1292702c.2432T>Ap.I811NSubstitution - Missense8:41942797-41942797-
TCGA-C8-A275-01COSM1489304c.3908A>Gp.D1303GSubstitution - Missense8:41934312-41934312-
TCGA-BR-4361-01COSM1099935c.2843G>Ap.R948QSubstitution - Missense8:41941038-41941038-
477COSM4438872c.5392C>Tp.H1798YSubstitution - Missense8:41932828-41932828-
57TCOSM5575806c.4618G>Ap.D1540NSubstitution - Missense8:41933602-41933602-
TCGA-BR-8680-01COSM3649304c.1456C>Tp.R486CSubstitution - Missense8:41974730-41974730-
TCGA-AA-A00N-01COSM276244c.2915G>Ap.R972HSubstitution - Missense8:41940966-41940966-
ME011TCOSM224344c.2356G>Ap.V786ISubstitution - Missense8:41942873-41942873-
LC_C27COSM1187532c.1708A>Gp.I570VSubstitution - Missense8:41949254-41949254-
LUAD-CHTN-MAD08-00104COSM361307c.3664G>Tp.E1222*Substitution - Nonsense8:41934556-41934556-
SW48COSM4656462c.4869C>Tp.S1623SSubstitution - coding silent8:41933351-41933351-
TCGA-46-3765-01COSM750340c.1953T>Gp.P651PSubstitution - coding silent8:41946634-41946634-
sysucc-1397TCOSM5475179c.2597G>Ap.G866DSubstitution - Missense8:41941284-41941284-
BD59TCOSM5498560c.355A>Gp.K119ESubstitution - Missense8:42048623-42048623-
STC246COSM5063212c.2214C>Tp.D738DSubstitution - coding silent8:41943762-41943762-
SH-9771COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
P100COSM188275c.3201C>Tp.I1067ISubstitution - coding silent8:41937407-41937407-
S01020COSM5665391c.783G>Tp.E261DSubstitution - Missense8:41981881-41981881-
BD107TCOSM5514449c.1902+9G>Tp.?Unknown8:41947742-41947742-
TCGA-EJ-5504-01COSM1132744c.2344T>Gp.S782ASubstitution - Missense8:41942885-41942885-
TCGA-D1-A103-01COSM1099928c.3386G>Ap.R1129QSubstitution - Missense8:41934834-41934834-
SH-9248COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
TCGA-AP-A056-01COSM1099893c.5530A>Cp.R1844RSubstitution - coding silent8:41932690-41932690-
8051717COSM1457133c.2912G>Ap.R971HSubstitution - Missense8:41940969-41940969-
SJOS004_DCOSM5023389c.2966_2968delAGGp.E993delEDeletion - In frame8:41940913-41940915-
ESO-K08COSM1258624c.1270C>Tp.R424WSubstitution - Missense8:41977101-41977101-
D11COSM4606483c.5539G>Tp.G1847WSubstitution - Missense8:41932681-41932681-
SNUH_G10_S1COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
TCGA-BP-4167-01COSM1137873c.3938A>Gp.D1313GSubstitution - Missense8:41934282-41934282-
Pat_36_BCOSM2961739c.1019delAp.N340fs*3Deletion - Frameshift8:41978666-41978666-
S03-09436-TPCOSM4993084c.5739C>Tp.S1913SSubstitution - coding silent8:41932481-41932481-
ESCC_35COSM5628717c.3257G>Tp.R1086LSubstitution - Missense8:41937351-41937351-
OCC06PTCOSM88606c.2392G>Cp.E798QSubstitution - Missense8:41942837-41942837-
YUKATCOSM5409623c.855C>Tp.D285DSubstitution - coding silent8:41980898-41980898-
TCGA-AP-A056-01COSM1099961c.876T>Cp.C292CSubstitution - coding silent8:41980877-41980877-
Gp2DCOSM605677c.1305G>Ap.E435ESubstitution - coding silent8:41977066-41977066-
BD72TCOSM5512479c.5098C>Tp.P1700SSubstitution - Missense8:41933122-41933122-
TCGA-HU-A4G9-01COSM3900243c.3244A>Cp.R1082RSubstitution - coding silent8:41937364-41937364-
SH-0622COSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
TCGA-EB-A41A-01COSM3649304c.1456C>Tp.R486CSubstitution - Missense8:41974730-41974730-
SNUH_G51_S1COSM3685393c.5073A>Tp.P1691PSubstitution - coding silent8:41933147-41933147-
SNU-C2BCOSM188274c.4427C>Tp.A1476VSubstitution - Missense8:41933793-41933793-
SH-9248COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
411COSM4431020c.4614A>Gp.V1538VSubstitution - coding silent8:41933606-41933606-
TCGA-AA-3715-01COSM269679c.5064G>Ap.Q1688QSubstitution - coding silent8:41933156-41933156-
P100COSM5009137c.3116C>Ap.S1039YSubstitution - Missense8:41937492-41937492-
CSCC-32-TCOSM4495064c.4454C>Tp.S1485FSubstitution - Missense8:41933766-41933766-
TCGA-AA-A010-01COSM283084c.5965G>Ap.A1989TSubstitution - Missense8:41932255-41932255-
2492730COSM5728500c.244C>Tp.L82FSubstitution - Missense8:42048734-42048734-
SWE-22COSM1179138c.2237T>Gp.I746SSubstitution - Missense8:41942992-41942992-
TCGA-QU-A6IO-01COSM4876558c.1013C>Tp.P338LSubstitution - Missense8:41978672-41978672-
082TCOSM1730929c.3481A>Gp.I1161VSubstitution - Missense8:41934739-41934739-
TCGA-BR-8680-01COSM188275c.3201C>Tp.I1067ISubstitution - coding silent8:41937407-41937407-
sysucc-1408TCOSM188273c.5722G>Ap.A1908TSubstitution - Missense8:41932498-41932498-
TCGA-EI-6917-01COSM3432439c.896G>Ap.R299HSubstitution - Missense8:41980857-41980857-
T3262COSM4694053c.5145T>Cp.P1715PSubstitution - coding silent8:41933075-41933075-
TCGA-56-6545-01COSM750345c.4532A>Tp.Q1511LSubstitution - Missense8:41933688-41933688-
TCGA-EE-A29D-06COSM227783c.1511C>Tp.P504LSubstitution - Missense8:41955383-41955383-
SH-7282COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
CSCC-38-TCOSM4544036c.3489G>Ap.W1163*Substitution - Nonsense8:41934731-41934731-
2521252COSM5889050c.5206C>Tp.P1736SSubstitution - Missense8:41933014-41933014-
LUAD-F00089COSM339908c.5954G>Ap.S1985NSubstitution - Missense8:41932266-41932266-
ESCC_57COSM5632459c.2528C>Tp.S843FSubstitution - Missense8:41941353-41941353-
BD204TCOSM5517835c.1563C>Gp.T521TSubstitution - coding silent8:41955331-41955331-
P100COSM5009140c.2103G>Ap.E701ESubstitution - coding silent8:41943873-41943873-
HCC174TCOSM3663765c.3798G>Ap.K1266KSubstitution - coding silent8:41934422-41934422-
TCGA-18-5592-01COSM750339c.1603C>Tp.P535SSubstitution - Missense8:41949359-41949359-
TCGA-BR-4257-01COSM3900245c.2863C>Ap.P955TSubstitution - Missense8:41941018-41941018-
6948_PTCOSM5757218c.2711A>Gp.E904GSubstitution - Missense8:41941170-41941170-
TCGA-HT-8015-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
CSCC-41-TCOSM4517377c.3305_3306GG>AAp.R1102KSubstitution - Missense8:41937302-41937303-
SH-7032COSM5020539c.147A>Gp.E49ESubstitution - coding silent8:42048831-42048831-
ESO-1670COSM1258621c.871G>Ap.E291KSubstitution - Missense8:41980882-41980882-
TCGA-B0-5695-01COSM188277c.2591G>Ap.R864QSubstitution - Missense8:41941290-41941290-
TCGA-AX-A0J0-01COSM1099949c.1615C>Tp.L539FSubstitution - Missense8:41949347-41949347-
TCGA-AP-A056-01COSM1099959c.1094A>Cp.K365TSubstitution - Missense8:41977277-41977277-
XHDG22CCOSM4767594c.3839C>Ap.S1280*Substitution - Nonsense8:41934381-41934381-
SCMC_RM2_COSM3900253c.751C>Tp.R251*Substitution - Nonsense8:41981913-41981913-
TCGA-EE-A29D-06COSM3649308c.686C>Tp.S229FSubstitution - Missense8:41987478-41987478-
PT33COSM5908852c.2437-3C>Tp.?Unknown8:41941447-41941447-
K-562COSM1673880c.5629C>Tp.R1877CSubstitution - Missense8:41932591-41932591-
TCGA-DK-A2I6-01COSM1314057c.4213G>Ap.E1405KSubstitution - Missense8:41934007-41934007-
Pat_06_ACOSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
SH-5693COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
PD4119aCOSM162772c.2302G>Cp.D768HSubstitution - Missense8:41942927-41942927-
TCGA-AA-A00N-01COSM276245c.1990G>Ap.D664NSubstitution - Missense8:41946597-41946597-
5_RESISTANTCOSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
HCC109TCOSM1624024c.3401A>Gp.K1134RSubstitution - Missense8:41934819-41934819-
C32COSM5037461c.2204G>Ap.R735QSubstitution - Missense8:41943772-41943772-
PT48COSM5932246c.4483C>Tp.R1495CSubstitution - Missense8:41933737-41933737-
TCGA-CD-8536-01COSM2961658c.5572C>Tp.R1858CSubstitution - Missense8:41932648-41932648-
TCGA-66-2785-01COSM750337c.1340C>Gp.S447*Substitution - Nonsense8:41977031-41977031-
585267COSM325901c.3632T>Gp.V1211GSubstitution - Missense8:41934588-41934588-
PD7211aCOSM5799851c.1502C>Ap.P501HSubstitution - Missense8:41955392-41955392-
C0100TCOSM4138709c.280A>Gp.K94ESubstitution - Missense8:42048698-42048698-
ME037TCOSM227783c.1511C>Tp.P504LSubstitution - Missense8:41955383-41955383-
CPCG0184-F1COSM3396732c.768G>Tp.R256RSubstitution - coding silent8:41981896-41981896-
SH-4435COSM5020145c.1488T>Cp.V496VSubstitution - coding silent8:41955406-41955406-
YUZESTCOSM1700046c.4592C>Tp.P1531LSubstitution - Missense8:41933628-41933628-
TCGA-F4-6807-01COSM1457139c.1572C>Tp.S524SSubstitution - coding silent8:41955322-41955322-
TCGA-P5-A5F2-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-60-2720-01COSM750342c.2629G>Tp.E877*Substitution - Nonsense8:41941252-41941252-
C089COSM5543042c.619C>Tp.P207SSubstitution - Missense8:41987545-41987545-
SH-2871COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
SJMB043COSM255263c.2981C>Tp.P994LSubstitution - Missense8:41940900-41940900-
ESO-1145COSM1258620c.2242C>Tp.R748CSubstitution - Missense8:41942987-41942987-
HCC88COSM1624022c.4772G>Tp.G1591VSubstitution - Missense8:41933448-41933448-
TCGA-BH-A0B6-01COSM3834736c.3758C>Tp.S1253FSubstitution - Missense8:41934462-41934462-
P46COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
2290929COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-C8-A27B-01COSM1489303c.5133C>Tp.F1711FSubstitution - coding silent8:41933087-41933087-
S02-14875-TPCOSM4993088c.2625C>Tp.T875TSubstitution - coding silent8:41941256-41941256-
SNU-175COSM1099963c.824C>Tp.A275VSubstitution - Missense8:41981840-41981840-
CHC902TCOSM5347548c.3077_3087del11p.R1026fs*2Deletion - Frameshift8:41937521-41937531-
TCGA-B0-5710-01COSM486472c.1988T>Cp.I663TSubstitution - Missense8:41946599-41946599-
sysucc-1370TCOSM188277c.2591G>Ap.R864QSubstitution - Missense8:41941290-41941290-
TCGA-CM-4746-01COSM1457142c.1041G>Ap.T347TSubstitution - coding silent8:41978644-41978644-
431COSM4433506c.4324G>Tp.A1442SSubstitution - Missense8:41933896-41933896-
T2258COSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
HCC048TCOSM5820523c.2711A>Tp.E904VSubstitution - Missense8:41941170-41941170-
TCGA-AP-A059-01COSM1099933c.3122C>Tp.T1041ISubstitution - Missense8:41937486-41937486-
SH-102782COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
Pat_31_BCOSM3900244c.3035G>Ap.R1012QSubstitution - Missense8:41940846-41940846-
T263COSM4694057c.3373G>Tp.V1125LSubstitution - Missense8:41934847-41934847-
2318492COSM4776934c.1133C>Tp.S378LSubstitution - Missense8:41977238-41977238-
HCC129TCOSM5817026c.4983G>Tp.P1661PSubstitution - coding silent8:41933237-41933237-
TCGA-BR-8487-01COSM3900237c.4742G>Ap.S1581NSubstitution - Missense8:41933478-41933478-
54COSM5734920c.5777G>Ap.R1926QSubstitution - Missense8:41932443-41932443-
TCGA-BR-8363-01COSM3900238c.4709A>Tp.D1570VSubstitution - Missense8:41933511-41933511-
TCGA-CH-5762-01COSM1472109c.614C>Tp.P205LSubstitution - Missense8:41987550-41987550-
TCGA-JW-A5VI-01COSM4829434c.2477C>Gp.S826CSubstitution - Missense8:41941404-41941404-
TCGA-D8-A3Z5-01COSM3834735c.5085T>Cp.P1695PSubstitution - coding silent8:41933135-41933135-
SH-7282COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
TCGA-39-5031-01COSM750346c.5563A>Tp.I1855FSubstitution - Missense8:41932657-41932657-
RK088_C01COSM3703405c.3178A>Gp.R1060GSubstitution - Missense8:41937430-41937430-
SH-5693COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
TCGA-AC-A23H-01COSM3834738c.1301C>Gp.S434CSubstitution - Missense8:41977070-41977070-
P100COSM2961689c.4183G>Ap.D1395NSubstitution - Missense8:41934037-41934037-
Pat_14_BCOSM5874704c.5510T>Cp.I1837TSubstitution - Missense8:41932710-41932710-
S00837COSM313087c.2836C>Gp.P946ASubstitution - Missense8:41941045-41941045-
ESO-2143COSM1258622c.5630G>Ap.R1877HSubstitution - Missense8:41932590-41932590-
HCC88TCOSM1624022c.4772G>Tp.G1591VSubstitution - Missense8:41933448-41933448-
2492711COSM5606649c.1689C>Tp.F563FSubstitution - coding silent8:41949273-41949273-
PT40COSM5923814c.4336T>Ap.C1446SSubstitution - Missense8:41933884-41933884-
TCGA-BR-A4QL-01COSM3900242c.3528T>Ap.S1176RSubstitution - Missense8:41934692-41934692-
CSCC-6-TCOSM4487881c.3240C>Tp.F1080FSubstitution - coding silent8:41937368-41937368-
P134COSM5010052c.1520G>Ap.R507HSubstitution - Missense8:41955374-41955374-
TCGA-ER-A193-06COSM3649305c.1428C>Tp.I476ISubstitution - coding silent8:41974758-41974758-
CHOL12COSM1743593c.2358C>Tp.V786VSubstitution - coding silent8:41942871-41942871-
CHC361TBCOSM3669907c.458G>Ap.R153HSubstitution - Missense8:42048520-42048520-
CN-AML-NR-15-DxCOSM5427331c.1968G>Ap.K656KSubstitution - coding silent8:41946619-41946619-
TCGA-BS-A0UJ-01COSM1099913c.4707C>Tp.Y1569YSubstitution - coding silent8:41933513-41933513-
TCGA-BS-A0UV-01COSM1099895c.5474C>Tp.S1825FSubstitution - Missense8:41932746-41932746-
TCGA-AZ-4315-01COSM276245c.1990G>Ap.D664NSubstitution - Missense8:41946597-41946597-
SH-7282COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
TCGA-D1-A17Q-01COSM1099924c.4192G>Ap.E1398KSubstitution - Missense8:41934028-41934028-
TCGA-CD-A4MG-01COSM3900236c.5189G>Tp.S1730ISubstitution - Missense8:41933031-41933031-
SA071COSM213307c.2525G>Cp.S842TSubstitution - Missense8:41941356-41941356-
sysucc-1370TCOSM2961748c.746C>Tp.T249MSubstitution - Missense8:41981918-41981918-
TCGA-AM-5821-01COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
P46COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
TCGA-G3-A25T-01COSM4941468c.1538A>Gp.E513GSubstitution - Missense8:41955356-41955356-
TCGA-ER-A19K-01COSM3649306c.1411T>Cp.F471LSubstitution - Missense8:41974775-41974775-
TCGA-MU-A51Y-01COSM4836594c.2992C>Tp.R998WSubstitution - Missense8:41940889-41940889-
ESCC_BICR_047TCOSM4753614c.1139A>Cp.E380ASubstitution - Missense8:41977232-41977232-
S02-14875-TPCOSM4993089c.1840C>Tp.L614FSubstitution - Missense8:41947813-41947813-
TCGA-FR-A3YO-06COSM3649309c.209C>Tp.S70FSubstitution - Missense8:42048769-42048769-
ESO-0067COSM1258618c.1133C>Gp.S378*Substitution - Nonsense8:41977238-41977238-
H1672COSM313085c.2439G>Tp.V813VSubstitution - coding silent8:41941442-41941442-
CHC1592TCOSM4791438c.4007C>Tp.P1336LSubstitution - Missense8:41934213-41934213-
TCGA-HU-A4H4-01COSM3900249c.2114A>Cp.H705PSubstitution - Missense8:41943862-41943862-
T3724COSM4694056c.3431C>Tp.T1144ISubstitution - Missense8:41934789-41934789-
PD4109aCOSM162771c.5920G>Ap.G1974RSubstitution - Missense8:41932300-41932300-
sysucc-880TCOSM5463727c.4952C>Ap.P1651QSubstitution - Missense8:41933268-41933268-
HCC97COSM1624025c.2601C>Tp.R867RSubstitution - coding silent8:41941280-41941280-
pfg008TCOSM1643601c.5378A>Gp.Q1793RSubstitution - Missense8:41932842-41932842-
TCGA-D3-A3C7-06COSM3649294c.4364C>Tp.T1455ISubstitution - Missense8:41933856-41933856-
SNU-175COSM2961684c.4606C>Tp.P1536SSubstitution - Missense8:41933614-41933614-
P100COSM5009138c.2701G>Tp.E901*Substitution - Nonsense8:41941180-41941180-
PD4109aCOSM162771c.5920G>Ap.G1974RSubstitution - Missense8:41932300-41932300-
SH-5693COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
Pa18CCOSM85115c.76C>Tp.R26CSubstitution - Missense8:42048902-42048902-
U2940COSM5621072c.2021G>Tp.G674VSubstitution - Missense8:41943955-41943955-
TCGA-AX-A0J0-01COSM1099955c.1437G>Tp.E479DSubstitution - Missense8:41974749-41974749-
TCGA-AX-A06H-01COSM1099963c.824C>Tp.A275VSubstitution - Missense8:41981840-41981840-
LP6005409-DNA_F02COSM4408613c.2830G>Cp.V944LSubstitution - Missense8:41941051-41941051-
P12COSM4753615c.1138G>Tp.E380*Substitution - Nonsense8:41977233-41977233-
TCGA-D8-A1JA-01COSM3834739c.334G>Cp.E112QSubstitution - Missense8:42048644-42048644-
TCGA-HT-8111-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-HE-A5NK-01COSM4908514c.3181T>Ap.L1061ISubstitution - Missense8:41937427-41937427-
PD8969aCOSM5789359c.2278C>Tp.L760FSubstitution - Missense8:41942951-41942951-
ESCC_13COSM5625364c.3187C>Ap.P1063TSubstitution - Missense8:41937421-41937421-
0059_CRUK_PC_0059_T1_DNACOSM5423060c.1900A>Tp.K634*Substitution - Nonsense8:41947753-41947753-
Gp5DCOSM605677c.1305G>Ap.E435ESubstitution - coding silent8:41977066-41977066-
SH-102782COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
TCGA-DD-A118-01COSM4937921c.1664A>Gp.Q555RSubstitution - Missense8:41949298-41949298-
TCGA-GN-A266-06COSM3649302c.2176G>Ap.D726NSubstitution - Missense8:41943800-41943800-
TCGA-EA-A3HT-01COSM4843404c.5972G>Ap.G1991DSubstitution - Missense8:41932248-41932248-
SWE-3ACOSM1178314c.1364-2A>Tp.?Unknown8:41974824-41974824-
1604875COSM141233c.4499C>Tp.P1500LSubstitution - Missense8:41933721-41933721-
2_PRE-TREATMENTCOSM1722310c.3116C>Tp.S1039FSubstitution - Missense8:41937492-41937492-
TCGA-AP-A0LF-01COSM1099937c.2833G>Ap.E945KSubstitution - Missense8:41941048-41941048-
T1743COSM4694052c.5327C>Tp.A1776VSubstitution - Missense8:41932893-41932893-
LAU50_1COSM235015c.2193C>Tp.L731LSubstitution - coding silent8:41943783-41943783-
PTC-7CCOSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
TCGA-EE-A2MM-06COSM110236c.1069C>Tp.R357*Substitution - Nonsense8:41977302-41977302-
CPCG_0184_Pr_P_F0COSM3396732c.768G>Tp.R256RSubstitution - coding silent8:41981896-41981896-
TCGA-B5-A0JY-01COSM1099901c.5351T>Cp.V1784ASubstitution - Missense8:41932869-41932869-
P12COSM4753614c.1139A>Cp.E380ASubstitution - Missense8:41977232-41977232-
TCGA-33-4586-01COSM750338c.1362A>Tp.T454TSubstitution - coding silent8:41977009-41977009-
LAU63COSM232843c.814G>Ap.G272SSubstitution - Missense8:41981850-41981850-
TCGA-AP-A0LM-01COSM1099926c.4189G>Ap.E1397KSubstitution - Missense8:41934031-41934031-
LP6005409-DNA_A01COSM5952036c.12C>Tp.L4LSubstitution - coding silent8:42048966-42048966-
TCGA-EE-A3AC-06COSM3649298c.3581C>Tp.S1194FSubstitution - Missense8:41934639-41934639-
CSCC-15-TCOSM4489889c.3548C>Tp.S1183FSubstitution - Missense8:41934672-41934672-
HCC83COSM3663764c.4997C>Tp.P1666LSubstitution - Missense8:41933223-41933223-
HCC83TCOSM3663764c.4997C>Tp.P1666LSubstitution - Missense8:41933223-41933223-
TCGA-G4-6625-01COSM1457130c.5245G>Ap.A1749TSubstitution - Missense8:41932975-41932975-
Pat_58_BCOSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
TCGA-DA-A1HY-06COSM3649295c.4008C>Tp.P1336PSubstitution - coding silent8:41934212-41934212-
LUAD_E01047COSM390322c.4720G>Tp.G1574CSubstitution - Missense8:41933500-41933500-
TCGA-AD-6889-01COSM1457129c.5684G>Ap.R1895HSubstitution - Missense8:41932536-41932536-
S0083COSM5884710c.3106G>Ap.E1036KSubstitution - Missense8:41937502-41937502-
Gp2DCOSM2961755c.575C>Tp.S192FSubstitution - Missense8:42048403-42048403-
TCGA-E5-A2PC-01COSM1314058c.3379C>Gp.L1127VSubstitution - Missense8:41934841-41934841-
TCGA-D7-8572-01COSM3900246c.2546A>Gp.Q849RSubstitution - Missense8:41941335-41941335-
Pat_70_BCOSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
TCGA-B5-A0JY-01COSM1099957c.1183G>Tp.D395YSubstitution - Missense8:41977188-41977188-
61COSM5738334c.3960T>Gp.D1320ESubstitution - Missense8:41934260-41934260-
TCGA-HU-A4H0-01COSM3900234c.5610C>Gp.H1870QSubstitution - Missense8:41932610-41932610-
S10-47754-TPCOSM4993086c.5299C>Tp.H1767YSubstitution - Missense8:41932921-41932921-
BCM703TCOSM4802957c.3127G>Tp.E1043*Substitution - Nonsense8:41937481-41937481-
LIM1215COSM255263c.2981C>Tp.P994LSubstitution - Missense8:41940900-41940900-
cSCCP6COSM136663c.3613C>Tp.Q1205*Substitution - Nonsense8:41934607-41934607-
LUAD-CHTN-MAD06-00668COSM360434c.1123G>Tp.A375SSubstitution - Missense8:41977248-41977248-
CPCG0259-F1COSM4880010c.1534A>Gp.I512VSubstitution - Missense8:41955360-41955360-
TCGA-DD-A119-01COSM4919921c.4316A>Gp.H1439RSubstitution - Missense8:41933904-41933904-
OSCC-GB_00990111COSM750339c.1603C>Tp.P535SSubstitution - Missense8:41949359-41949359-
SH-2871COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
SH-2871COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
PT17_1COSM5898952c.4748C>Tp.S1583FSubstitution - Missense8:41933472-41933472-
SH-102782COSM5021116c.600+5G>Tp.?Unknown8:42048373-42048373-
HF-23896COSM1197530c.5668G>Ap.A1890TSubstitution - Missense8:41932552-41932552-
SH-9161COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
Gp5DCOSM2961750c.699T>Cp.C233CSubstitution - coding silent8:41987465-41987465-
TCGA-BR-7707-01COSM360434c.1123G>Tp.A375SSubstitution - Missense8:41977248-41977248-
1946219COSM1197530c.5668G>Ap.A1890TSubstitution - Missense8:41932552-41932552-
TCGA-18-3408-01COSM750332c.623T>Cp.I208TSubstitution - Missense8:41987541-41987541-
TCGA-CD-A4MG-01COSM3900248c.2345C>Tp.S782FSubstitution - Missense8:41942884-41942884-
TCGA-AP-A059-01COSM1099891c.5747T>Cp.M1916TSubstitution - Missense8:41932473-41932473-
TCGA-AN-A046-01COSM3834737c.3013C>Ap.L1005ISubstitution - Missense8:41940868-41940868-
1517_PTCOSM5757217c.3720G>Tp.E1240DSubstitution - Missense8:41934500-41934500-
TCGA-EE-A2MD-06COSM2961664c.5336C>Tp.S1779FSubstitution - Missense8:41932884-41932884-
S00501COSM313086c.473G>Ap.G158DSubstitution - Missense8:42048505-42048505-
HCC90COSM1624023c.4504G>Ap.V1502MSubstitution - Missense8:41933716-41933716-
S00837COSM313087c.2836C>Gp.P946ASubstitution - Missense8:41941045-41941045-
HN_62506COSM124650c.3455G>Tp.W1152LSubstitution - Missense8:41934765-41934765-
HCC97COSM1624026c.2600G>Tp.R867LSubstitution - Missense8:41941281-41941281-
TCGA-BR-A4QL-01COSM3900255c.428T>Gp.F143CSubstitution - Missense8:42048550-42048550-
3N48-VS-3T48COSM4982812c.525C>Tp.N175NSubstitution - coding silent8:42048453-42048453-
HCC174COSM3663765c.3798G>Ap.K1266KSubstitution - coding silent8:41934422-41934422-
1731645COSM327857c.3071G>Cp.R1024PSubstitution - Missense8:41937537-41937537-
SH-9771COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
TCGA-FW-A3TU-06COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-P5-A5F0-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-33-4582-01COSM750336c.1190A>Gp.N397SSubstitution - Missense8:41977181-41977181-
TCGA-AA-3989-01COSM298010c.3593C>Tp.A1198VSubstitution - Missense8:41934627-41934627-
TCGA-GF-A6C9-06COSM4903655c.1138G>Ap.E380KSubstitution - Missense8:41977233-41977233-
TCGA-18-3409-01COSM750341c.2259C>Tp.I753ISubstitution - coding silent8:41942970-41942970-
134430COSM325900c.1398T>Ap.N466KSubstitution - Missense8:41974788-41974788-
S06-38853-TPCOSM4993087c.4610C>Tp.S1537FSubstitution - Missense8:41933610-41933610-
PT38COSM5922681c.3241C>Tp.P1081SSubstitution - Missense8:41937367-41937367-
TCGA-66-2785-01COSM750333c.883C>Gp.P295ASubstitution - Missense8:41980870-41980870-
pfg181TCOSM4753615c.1138G>Tp.E380*Substitution - Nonsense8:41977233-41977233-
TCGA-AX-A05Z-01COSM1099899c.5370A>Cp.G1790GSubstitution - coding silent8:41932850-41932850-
PT37COSM4495064c.4454C>Tp.S1485FSubstitution - Missense8:41933766-41933766-
203TCOSM5576205c.2842C>Tp.R948*Substitution - Nonsense8:41941039-41941039-
TCGA-GF-A4EO-06COSM3649293c.4482C>Tp.V1494VSubstitution - coding silent8:41933738-41933738-
S00501COSM313086c.473G>Ap.G158DSubstitution - Missense8:42048505-42048505-
TCGA-HT-A5RA-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-AM-5821-01COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
BCM703TCOSM4802957c.3127G>Tp.E1043*Substitution - Nonsense8:41937481-41937481-
TCGA-66-2785-01COSM750334c.1087G>Tp.G363CSubstitution - Missense8:41977284-41977284-
CPCG0201-F1COSM4879901c.1480C>Tp.Q494*Substitution - Nonsense8:41974706-41974706-
TCGA-BS-A0UJ-01COSM1099953c.1482+2T>Cp.?Unknown8:41974702-41974702-
CSCC-42-TCOSM4479138c.229C>Tp.P77SSubstitution - Missense8:42048749-42048749-
TCGA-AA-A00N-01COSM276243c.4487C>Tp.S1496LSubstitution - Missense8:41933733-41933733-
TCGA-AZ-6598-01COSM1457131c.5078_5079insCp.P1694fs*13Insertion - Frameshift8:41933141-41933142-
TCGA-B5-A11E-01COSM1099909c.5049G>Ap.P1683PSubstitution - coding silent8:41933171-41933171-
TCGA-B5-A11E-01COSM1099905c.5103G>Ap.P1701PSubstitution - coding silent8:41933117-41933117-
TCGA-CU-A0YR-01COSM422121c.3244A>Gp.R1082GSubstitution - Missense8:41937364-41937364-
TCGA-EB-A3Y7-01COSM3649296c.3756C>Tp.A1252ASubstitution - coding silent8:41934464-41934464-
C086COSM5532989c.4611C>Tp.S1537SSubstitution - coding silent8:41933609-41933609-
2492714COSM5606649c.1689C>Tp.F563FSubstitution - coding silent8:41949273-41949273-
TCGA-BR-7703-01COSM3900253c.751C>Tp.R251*Substitution - Nonsense8:41981913-41981913-
WM3211COSM3727435c.4736G>Ap.G1579ESubstitution - Missense8:41933484-41933484-
234COSM3730486c.2934G>Ap.R978RSubstitution - coding silent8:41940947-41940947-
ESO-2143COSM1258623c.4145C>Tp.T1382MSubstitution - Missense8:41934075-41934075-
2_RESISTANTCOSM1722310c.3116C>Tp.S1039FSubstitution - Missense8:41937492-41937492-
TCGA-B9-5155-01COSM3996065c.3198G>Tp.E1066DSubstitution - Missense8:41937410-41937410-
HCC004TCOSM5803341c.5115T>Cp.C1705CSubstitution - coding silent8:41933105-41933105-
TCGA-AP-A056-01COSM1099935c.2843G>Ap.R948QSubstitution - Missense8:41941038-41941038-
pfg008TCOSM1643601c.5378A>Gp.Q1793RSubstitution - Missense8:41932842-41932842-
TCGA-FW-A3R5-06COSM3925327c.734C>Tp.S245FSubstitution - Missense8:41981930-41981930-
CRC-29TCOSM5452242c.3577G>Ap.V1193ISubstitution - Missense8:41934643-41934643-
ESO-0459COSM750343c.2996C>Gp.S999*Substitution - Nonsense8:41940885-41940885-
TCGA-FW-A3R5-06COSM3649297c.3586C>Tp.P1196SSubstitution - Missense8:41934634-41934634-
TCGA-D1-A167-01COSM1099917c.4651A>Gp.S1551GSubstitution - Missense8:41933569-41933569-
CSCC-27-TCOSM4566800c.4763_4764CC>TTp.S1588FSubstitution - Missense8:41933456-41933457-
TCGA-BS-A0UV-01COSM188275c.3201C>Tp.I1067ISubstitution - coding silent8:41937407-41937407-
8062306COSM85115c.76C>Tp.R26CSubstitution - Missense8:42048902-42048902-
CHC909TCOSM5348609c.5810_5811insTp.S1938fs*1Insertion - Frameshift8:41932409-41932410-
YUTRAINCOSM3649293c.4482C>Tp.V1494VSubstitution - coding silent8:41933738-41933738-
TCGA-22-5477-01COSM750335c.1108C>Tp.L370FSubstitution - Missense8:41977263-41977263-
pfg008TCOSM1643602c.2046G>Ap.P682PSubstitution - coding silent8:41943930-41943930-
465COSM4437159c.110C>Ap.S37YSubstitution - Missense8:42048868-42048868-
TCGA-BR-7703-01COSM3900252c.986G>Ap.R329QSubstitution - Missense8:41978699-41978699-
TCGA-ER-A3EV-06COSM3925326c.2056C>Gp.L686VSubstitution - Missense8:41943920-41943920-
TCGA-FD-A3SS-01COSM3779231c.191C>Gp.S64*Substitution - Nonsense8:42048787-42048787-
ME016TCOSM224958c.2390G>Ap.G797ESubstitution - Missense8:41942839-41942839-
TCGA-BP-4177-01COSM1496901c.2219G>Tp.R740LSubstitution - Missense8:41943757-41943757-
587362COSM1216526c.3893C>Tp.P1298LSubstitution - Missense8:41934327-41934327-
TCGA-BH-A18G-01COSM5218315c.3865_3867delGAGp.E1289delEDeletion - In frame8:41934353-41934355-
YUKLABCOSM1700048c.2116C>Tp.Q706*Substitution - Nonsense8:41943860-41943860-
TCGA-EI-6917-01COSM1099928c.3386G>Ap.R1129QSubstitution - Missense8:41934834-41934834-
TCGA-D7-A4YY-01COSM3900250c.1279C>Tp.R427WSubstitution - Missense8:41977092-41977092-
LUAD-CHTN-MAD06-00668COSM360433c.4754G>Tp.S1585ISubstitution - Missense8:41933466-41933466-
CHC1592TCOSM4791438c.4007C>Tp.P1336LSubstitution - Missense8:41934213-41934213-
T368COSM4694055c.3807_3808insCCAp.E1269_V1270insPInsertion - In frame8:41934412-41934413-
P100COSM5009136c.4692G>Tp.E1564DSubstitution - Missense8:41933528-41933528-
3030_TCOSM3951681c.4790G>Ap.S1597NSubstitution - Missense8:41933430-41933430-
TCGA-CM-6171-01COSM1457133c.2912G>Ap.R971HSubstitution - Missense8:41940969-41940969-
12TCOSM110236c.1069C>Tp.R357*Substitution - Nonsense8:41977302-41977302-
C135COSM4611233c.1251delTp.F417fs*61Deletion - Frameshift8:41977120-41977120-
TCGA-BR-8297-01COSM2961742c.994A>Gp.T332ASubstitution - Missense8:41978691-41978691-
ESCC_BICR_018TCOSM5429111c.953A>Cp.K318TSubstitution - Missense8:41978732-41978732-
PD18149aCOSM5800895c.4639G>Tp.D1547YSubstitution - Missense8:41933581-41933581-
P100COSM5009139c.2590C>Tp.R864WSubstitution - Missense8:41941291-41941291-
CHC1744TCOSM3396732c.768G>Tp.R256RSubstitution - coding silent8:41981896-41981896-
TCGA-09-2049-01COSM71772c.1753G>Ap.V585MSubstitution - Missense8:41947900-41947900-
TCGA-BG-A0M4-01COSM1099915c.4660G>Tp.G1554CSubstitution - Missense8:41933560-41933560-
2250164COSM5030177c.3754G>Ap.A1252TSubstitution - Missense8:41934466-41934466-
LIM2405COSM4643256c.5407A>Tp.T1803SSubstitution - Missense8:41932813-41932813-
TCGA-BP-5181-01COSM1496902c.5333C>Ap.T1778NSubstitution - Missense8:41932887-41932887-
S04-45633-TPCOSM4993085c.5737T>Gp.S1913ASubstitution - Missense8:41932483-41932483-
Br27PCOSM40361c.1575C>Tp.S525SSubstitution - coding silent8:41955319-41955319-
HCC129TCOSM5817096c.4984C>Tp.P1662SSubstitution - Missense8:41933236-41933236-
587316COSM1216525c.3260G>Ap.R1087HSubstitution - Missense8:41937348-41937348-
TCGA-D1-A0ZO-01COSM1099903c.5226C>Tp.G1742GSubstitution - coding silent8:41932994-41932994-
TCGA-13-0904-01COSM71773c.1367A>Gp.N456SSubstitution - Missense8:41974819-41974819-
C089COSM4895419c.618C>Tp.I206ISubstitution - coding silent8:41987546-41987546-
T3225COSM4694059c.2790C>Tp.D930DSubstitution - coding silent8:41941091-41941091-
TCGA-EE-A2ML-06COSM3649297c.3586C>Tp.P1196SSubstitution - Missense8:41934634-41934634-
tumor_4166503COSM5950195c.1740+4A>Gp.?Unknown8:41949218-41949218-
HCC118TCOSM5813825c.318A>Tp.A106ASubstitution - coding silent8:42048660-42048660-
TCGA-CD-A4MI-01COSM3432438c.932G>Ap.R311QSubstitution - Missense8:41978753-41978753-
TCGA-BR-8680-01COSM3900233c.5742G>Ap.M1914ISubstitution - Missense8:41932478-41932478-
SH-9161COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
GHE0536COSM5713901c.5404G>Ap.G1802RSubstitution - Missense8:41932816-41932816-
PD8969aCOSM5796943c.2277G>Tp.K759NSubstitution - Missense8:41942952-41942952-
PD7240aCOSM188304c.131G>Ap.R44HSubstitution - Missense8:42048847-42048847-
HCC90TCOSM1624023c.4504G>Ap.V1502MSubstitution - Missense8:41933716-41933716-
TCGA-EE-A29M-06COSM3649291c.5386C>Tp.P1796SSubstitution - Missense8:41932834-41932834-
T3174COSM4694060c.1813A>Cp.T605PSubstitution - Missense8:41947840-41947840-
TCGA-BT-A2LA-01COSM1314059c.2186C>Gp.S729CSubstitution - Missense8:41943790-41943790-
SC_9008COSM5563822c.1665G>Ap.Q555QSubstitution - coding silent8:41949297-41949297-
TCGA-85-6560-01COSM750344c.3576C>Tp.I1192ISubstitution - coding silent8:41934644-41934644-
T155COSM1176468c.4654G>Tp.D1552YSubstitution - Missense8:41933566-41933566-
TCGA-AM-5821-01COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
LAU50_2COSM235015c.2193C>Tp.L731LSubstitution - coding silent8:41943783-41943783-
7TCOSM5575643c.830A>Gp.N277SSubstitution - Missense8:41980923-41980923-
TCGA-RP-A693-06COSM4895419c.618C>Tp.I206ISubstitution - coding silent8:41987546-41987546-
P46COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
TCGA-61-1727-01COSM1330978c.4261G>Cp.D1421HSubstitution - Missense8:41933959-41933959-
S02299COSM5690950c.2806C>Tp.P936SSubstitution - Missense8:41941075-41941075-
LC_S32COSM1187529c.4576A>Cp.N1526HSubstitution - Missense8:41933644-41933644-
P100COSM3432438c.932G>Ap.R311QSubstitution - Missense8:41978753-41978753-
B22COSM1755725c.5121G>Ap.M1707ISubstitution - Missense8:41933099-41933099-
TCGA-BF-A1Q0-01COSM3649300c.2853C>Gp.L951LSubstitution - coding silent8:41941028-41941028-
TCGA-AZ-4682-01COSM1197530c.5668G>Ap.A1890TSubstitution - Missense8:41932552-41932552-
TCGA-AX-A05Z-01COSM1099941c.2647G>Tp.D883YSubstitution - Missense8:41941234-41941234-
TCGA-CG-5726-01COSM3900241c.3661G>Ap.E1221KSubstitution - Missense8:41934559-41934559-
TCGA-FR-A3R1-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
23_FLCOSM4171816c.2816G>Cp.R939TSubstitution - Missense8:41941065-41941065-
TCGA-HU-8602-01COSM3900239c.4367T>Cp.L1456PSubstitution - Missense8:41933853-41933853-
CHC1744TCOSM3396732c.768G>Tp.R256RSubstitution - coding silent8:41981896-41981896-
GHE0776COSM1673880c.5629C>Tp.R1877CSubstitution - Missense8:41932591-41932591-
TCGA-B5-A0JY-01COSM1099928c.3386G>Ap.R1129QSubstitution - Missense8:41934834-41934834-
Pat_31_ACOSM3900244c.3035G>Ap.R1012QSubstitution - Missense8:41940846-41940846-
2492712COSM5606649c.1689C>Tp.F563FSubstitution - coding silent8:41949273-41949273-
S02-14875-TPCOSM4993090c.189C>Tp.V63VSubstitution - coding silent8:42048789-42048789-
LC_C6COSM1187531c.3121A>Tp.T1041SSubstitution - Missense8:41937487-41937487-
TCGA-C5-A1BK-01COSM4437159c.110C>Ap.S37YSubstitution - Missense8:42048868-42048868-
TCGA-CU-A3YL-01COSM3779230c.5221G>Tp.A1741SSubstitution - Missense8:41932999-41932999-
TP_2009COSM5563368c.5655G>Cp.Q1885HSubstitution - Missense8:41932565-41932565-
ESO-1096COSM1258619c.3026C>Tp.T1009MSubstitution - Missense8:41940855-41940855-
EGC15COSM5063211c.4806C>Tp.S1602SSubstitution - coding silent8:41933414-41933414-
TCGA-DA-A1HV-06COSM3649303c.2166C>Tp.I722ISubstitution - coding silent8:41943810-41943810-
TCGA-D3-A2JH-06COSM40361c.1575C>Tp.S525SSubstitution - coding silent8:41955319-41955319-
TCGA-AX-A05Z-01COSM1099889c.5982G>Ap.K1994KSubstitution - coding silent8:41932238-41932238-
2530678COSM5885870c.644delCp.T215fs*28Deletion - Frameshift8:41987520-41987520-
SNU-C1COSM2961712c.2259C>Gp.I753MSubstitution - Missense8:41942970-41942970-
Gp5DCOSM2961755c.575C>Tp.S192FSubstitution - Missense8:42048403-42048403-
pfg277TCOSM4753610c.4833C>Ap.S1611RSubstitution - Missense8:41933387-41933387-
HCC97TCOSM1624026c.2600G>Tp.R867LSubstitution - Missense8:41941281-41941281-
TCGA-F1-6874-01COSM3900247c.2401G>Cp.E801QSubstitution - Missense8:41942828-41942828-
Pat_36_BCOSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
Pat_74_ACOSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
TCGA-D3-A2J7-06COSM3649301c.2724C>Tp.A908ASubstitution - coding silent8:41941157-41941157-
2_PRE-TREATMENTCOSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
ACINAR28COSM1734526c.5635C>Ap.P1879TSubstitution - Missense8:41932585-41932585-
TCGA-BP-5198-01COSM486470c.4164G>Cp.Q1388HSubstitution - Missense8:41934056-41934056-
07-058COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
Single_SampleCOSM4606483c.5539G>Tp.G1847WSubstitution - Missense8:41932681-41932681-
1781COSM1644803c.5735A>Gp.N1912SSubstitution - Missense8:41932485-41932485-
SH-102782COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
TCGA-HU-A4GU-01COSM3900240c.4323C>Tp.G1441GSubstitution - coding silent8:41933897-41933897-
392COSM4428344c.2534G>Ap.R845HSubstitution - Missense8:41941347-41941347-
Pat_53_ACOSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
WSU-HN8COSM4602831c.4916T>Cp.V1639ASubstitution - Missense8:41933304-41933304-
HCC2998COSM173599c.4222G>Ap.E1408KSubstitution - Missense8:41933998-41933998-
TCGA-CC-A7IH-01COSM4923320c.2586A>Gp.P862PSubstitution - coding silent8:41941295-41941295-
LUAD-RT-S01702COSM379452c.3691G>Ap.A1231TSubstitution - Missense8:41934529-41934529-
TCGA-A8-A093-01COSM454577c.3506G>Ap.R1169QSubstitution - Missense8:41934714-41934714-
TCGA-D7-6524-01COSM3900256c.405C>Ap.F135LSubstitution - Missense8:42048573-42048573-
TCGA-AX-A05Z-01COSM1099945c.2144A>Cp.K715TSubstitution - Missense8:41943832-41943832-
5_PRE-TREATMENTCOSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
18195COSM1314058c.3379C>Gp.L1127VSubstitution - Missense8:41934841-41934841-
HCT-15COSM1673881c.5240C>Ap.P1747QSubstitution - Missense8:41932980-41932980-
TCGA-EE-A29E-06COSM3649290c.5427C>Tp.T1809TSubstitution - coding silent8:41932793-41932793-
T407COSM4694054c.3946G>Ap.A1316TSubstitution - Missense8:41934274-41934274-
YURIDACOSM1700047c.3865G>Tp.E1289*Substitution - Nonsense8:41934355-41934355-
LC_C4COSM1187530c.3943G>Ap.D1315NSubstitution - Missense8:41934277-41934277-
tumor_4135099COSM2961703c.3162C>Tp.S1054SSubstitution - coding silent8:41937446-41937446-
P13COSM5009608c.4226T>Gp.L1409*Substitution - Nonsense8:41933994-41933994-
2492713COSM5606649c.1689C>Tp.F563FSubstitution - coding silent8:41949273-41949273-
T3094COSM4694062c.432C>Tp.H144HSubstitution - coding silent8:42048546-42048546-
SH-9248COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
TCGA-F5-6814-01COSM3432438c.932G>Ap.R311QSubstitution - Missense8:41978753-41978753-
TCGA-K4-A3WU-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-BR-A4CS-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
Au3COSM5601664c.4136C>Tp.S1379FSubstitution - Missense8:41934084-41934084-
TCGA-EE-A181-06COSM3649310c.93G>Ap.R31RSubstitution - coding silent8:42048885-42048885-
YUOTHOCOSM5409621c.2741C>Tp.T914ISubstitution - Missense8:41941140-41941140-
sysucc-1370TCOSM5472591c.4767C>Tp.Y1589YSubstitution - coding silent8:41933453-41933453-
TCGA-34-2600-01COSM750343c.2996C>Gp.S999*Substitution - Nonsense8:41940885-41940885-
TCGA-BR-7197-01COSM3900257c.331G>Tp.A111SSubstitution - Missense8:42048647-42048647-
Pat_60_BCOSM2961739c.1019delAp.N340fs*3Deletion - Frameshift8:41978666-41978666-
I2L-P19Ta-Tumor-BiopsyCOSM5358724c.3871C>Tp.Q1291*Substitution - Nonsense8:41934349-41934349-
LUAD-S01320COSM346190c.2447C>Gp.S816CSubstitution - Missense8:41941434-41941434-
TCGA-BH-A18P-01COSM454578c.2811G>Cp.K937NSubstitution - Missense8:41941070-41941070-
TCGA-DW-7837-01COSM3996064c.3796A>Cp.K1266QSubstitution - Missense8:41934424-41934424-
SS6003305COSM3983753c.4108G>Ap.E1370KSubstitution - Missense8:41934112-41934112-
SH-1537COSM4694058c.2977_2979delGAGp.E993delEDeletion - In frame8:41940902-41940904-
TCGA-AP-A056-01COSM1099930c.3270G>Ap.S1090SSubstitution - coding silent8:41937338-41937338-
TCGA-CZ-4853-01COSM486471c.3449A>Cp.K1150TSubstitution - Missense8:41934771-41934771-
HT115COSM2961700c.3497G>Tp.R1166ISubstitution - Missense8:41934723-41934723-
49MCOSM3925327c.734C>Tp.S245FSubstitution - Missense8:41981930-41981930-
SH-7032COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
PD5932aCOSM5778529c.5793G>Ap.M1931ISubstitution - Missense8:41932427-41932427-
TCGA-B0-5099-01COSM486473c.985C>Tp.R329WSubstitution - Missense8:41978700-41978700-
YUKADICOSM1700045c.5162C>Tp.P1721LSubstitution - Missense8:41933058-41933058-
TCGA-DA-A1I5-06COSM3649307c.1101A>Tp.K367NSubstitution - Missense8:41977270-41977270-
BK0019COSM4186146c.3522G>Tp.K1174NSubstitution - Missense8:41934698-41934698-
2293776COSM4608017c.5761G>Tp.A1921SSubstitution - Missense8:41932459-41932459-
HCT15COSM1673881c.5240C>Ap.P1747QSubstitution - Missense8:41932980-41932980-
PT44COSM5926627c.5485C>Tp.Q1829*Substitution - Nonsense8:41932735-41932735-
LP6007398-DNA_A01COSM5951771c.5850T>Gp.P1950PSubstitution - coding silent8:41932370-41932370-
ESCC_BICR_047TCOSM4753615c.1138G>Tp.E380*Substitution - Nonsense8:41977233-41977233-
B22-TumorCOSM1755725c.5121G>Ap.M1707ISubstitution - Missense8:41933099-41933099-
TCGA-HU-8602-01COSM3900244c.3035G>Ap.R1012QSubstitution - Missense8:41940846-41940846-
CN-AML-15-TCOSM5427331c.1968G>Ap.K656KSubstitution - coding silent8:41946619-41946619-
61COSM5738335c.1262C>Ap.P421HSubstitution - Missense8:41977109-41977109-
TCGA-AX-A05Z-01COSM1099921c.4442G>Ap.S1481NSubstitution - Missense8:41933778-41933778-
TCGA-13-0714-01COSM78139c.2019A>Cp.E673DSubstitution - Missense8:41943957-41943957-
CSCC-44-TCOSM4490577c.3660C>Tp.P1220PSubstitution - coding silent8:41934560-41934560-
TCGA-AX-A0J0-01COSM1099943c.2398G>Ap.E800KSubstitution - Missense8:41942831-41942831-
SNUH_G10_S1COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
tumor_4159421COSM5946584c.1858C>Tp.Q620*Substitution - Nonsense8:41947795-41947795-
HCC143TCOSM5811372c.3369G>Ap.K1123KSubstitution - coding silent8:41934851-41934851-
PT46COSM5929051c.5978C>Tp.P1993LSubstitution - Missense8:41932242-41932242-
TCGA-EI-6917-01COSM1187530c.3943G>Ap.D1315NSubstitution - Missense8:41934277-41934277-
TCGA-ER-A19F-06COSM3649299c.3429C>Ap.S1143SSubstitution - coding silent8:41934791-41934791-
TCGA-AM-5820-01COSM5134633c.4989_4991delGCCp.P1664delPDeletion - In frame8:41933229-41933231-
TCGA-HT-A5R5-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-23-2645-01COSM1330977c.3527G>Cp.S1176TSubstitution - Missense8:41934693-41934693-
19COSM188274c.4427C>Tp.A1476VSubstitution - Missense8:41933793-41933793-
SH-9771COSM3763348c.2982G>Ap.P994PSubstitution - coding silent8:41940899-41940899-
TCGA-B5-A11E-01COSM1099897c.5433G>Ap.T1811TSubstitution - coding silent8:41932787-41932787-
sysucc-1577TCOSM5764745c.4892G>Ap.S1631NSubstitution - Missense8:41933328-41933328-
TCGA-RP-A694-06COSM4894215c.4397C>Tp.P1466LSubstitution - Missense8:41933823-41933823-
TCGA-DI-A0WH-01COSM1099951c.1529C>Gp.S510CSubstitution - Missense8:41955365-41955365-
HCC2998COSM173599c.4222G>Ap.E1408KSubstitution - Missense8:41933998-41933998-
I2L-P20-Tumor-BiopsyCOSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
HCC109COSM1624024c.3401A>Gp.K1134RSubstitution - Missense8:41934819-41934819-
TCGA-CM-4743-01COSM1457132c.3727delGp.D1243fs*51Deletion - Frameshift8:41934493-41934493-
RKOCOSM2961758c.472G>Ap.G158SSubstitution - Missense8:42048506-42048506-
16246COSM5615992c.5659G>Tp.G1887CSubstitution - Missense8:41932561-41932561-
TCGA-AA-A01Q-01COSM300091c.2452T>Cp.S818PSubstitution - Missense8:41941429-41941429-
SH-9161COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
C0081TCOSM4138708c.2717C>Tp.S906LSubstitution - Missense8:41941164-41941164-
TCGA-BS-A0TC-01COSM1099911c.4708G>Ap.D1570NSubstitution - Missense8:41933512-41933512-
TCGA-HT-7477-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
587238COSM1216524c.2096T>Cp.I699TSubstitution - Missense8:41943880-41943880-
RK256_C01COSM4945774c.4393G>Tp.D1465YSubstitution - Missense8:41933827-41933827-
T96COSM4694061c.1096C>Tp.R366*Substitution - Nonsense8:41977275-41977275-
TCGA-HU-A4H3-01COSM188275c.3201C>Tp.I1067ISubstitution - coding silent8:41937407-41937407-
BD236TCOSM5518836c.4629G>Ap.Q1543QSubstitution - coding silent8:41933591-41933591-
2530678COSM5885539c.4348C>Gp.L1450VSubstitution - Missense8:41933872-41933872-
10821COSM3728123c.4766A>Gp.Y1589CSubstitution - Missense8:41933454-41933454-
pfg181TCOSM4753614c.1139A>Cp.E380ASubstitution - Missense8:41977232-41977232-
ESO-859COSM1239540c.4673G>Ap.S1558NSubstitution - Missense8:41933547-41933547-
ccRCC-75COSM1662351c.2626C>Ap.Q876KSubstitution - Missense8:41941255-41941255-
TCGA-BS-A0UV-01COSM173599c.4222G>Ap.E1408KSubstitution - Missense8:41933998-41933998-
9149_TCOSM5041508c.355A>Cp.K119QSubstitution - Missense8:42048623-42048623-
079TCOSM1730771c.3443A>Tp.K1148MSubstitution - Missense8:41934777-41934777-
Au8COSM5606649c.1689C>Tp.F563FSubstitution - coding silent8:41949273-41949273-
2521252COSM4495064c.4454C>Tp.S1485FSubstitution - Missense8:41933766-41933766-
TCGA-BS-A0UM-01COSM1099947c.2063G>Ap.R688HSubstitution - Missense8:41943913-41943913-
1517_CLMCOSM5757217c.3720G>Tp.E1240DSubstitution - Missense8:41934500-41934500-
SJMB013COSM255769c.2965_2967delGAGp.E993delEDeletion - In frame8:41940914-41940916-
TCGA-AP-A0LM-01COSM1099965c.4G>Ap.V2ISubstitution - Missense8:42048974-42048974-
LP6005409-DNA_A01COSM5952075c.1504C>Tp.P502SSubstitution - Missense8:41955390-41955390-
PT21_2COSM1216526c.3893C>Tp.P1298LSubstitution - Missense8:41934327-41934327-
SH-7032COSM3763347c.4455C>Tp.S1485SSubstitution - coding silent8:41933765-41933765-
PT23_2COSM5903681c.4118C>Tp.S1373FSubstitution - Missense8:41934102-41934102-
OSCC-GB_00620111COSM4881353c.2999G>Tp.S1000ISubstitution - Missense8:41940882-41940882-
TCGA-BR-8361-01COSM3900251c.1131A>Gp.S377SSubstitution - coding silent8:41977240-41977240-
TCGA-EE-A29D-06COSM3649292c.5377C>Tp.Q1793*Substitution - Nonsense8:41932843-41932843-
TCGA-HU-A4H3-01COSM3900258c.13G>Ap.A5TSubstitution - Missense8:42048965-42048965-
TCGA-AP-A059-01COSM1099919c.4473C>Tp.S1491SSubstitution - coding silent8:41933747-41933747-
SH-7032COSM3736469c.401T>Cp.L134SSubstitution - Missense8:42048577-42048577-
TCGA-P5-A5F4-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-D8-A3Z5-01COSM1722309c.5079A>Cp.P1693PSubstitution - coding silent8:41933141-41933141-
TCGA-AP-A0LF-01COSM1099939c.2770G>Ap.E924KSubstitution - Missense8:41941111-41941111-
YUKLABCOSM1700049c.2009C>Tp.S670LSubstitution - Missense8:41943967-41943967-
HCC97TCOSM1624025c.2601C>Tp.R867RSubstitution - coding silent8:41941280-41941280-
1604875COSM141234c.80C>Tp.P27LSubstitution - Missense8:42048898-42048898-
I2L-P19Ta-Tumor-OrganoidCOSM5358724c.3871C>Tp.Q1291*Substitution - Nonsense8:41934349-41934349-
2367114COSM4997293c.947G>Cp.G316ASubstitution - Missense8:41978738-41978738-
PD4109aCOSM162771c.5920G>Ap.G1974RSubstitution - Missense8:41932300-41932300-
YUSCACOSM5409622c.2592G>Ap.R864RSubstitution - coding silent8:41941289-41941289-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.491548;Hs.4915778p11601408
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AC5-UTRSNV.c.1-683T>G841907178HC
ACIntronicSNV.c.1483-2256T>G841815185HC
ACMissensep.S782Ac.2344T>G841800403PRAD
ACMissensep.V1211Gc.3632T>G841792106SCLC
ACSynonymousp.P651Pc.1953T>G841804152LUSC
AGMissensep.F471Lc.1411T>C841832293CM
AGMissensep.I208Tc.623T>C841845059LUSC
AGMissensep.I663Tc.1988T>C841804117RCCC
ATMissensep.I811Nc.2432T>A841800315CLL
ATMissensep.N466Kc.1398T>A841832306SCLC
ATNonsensep.C590*c.1770T>A841805401CM
C-5-UTRDeletion.c.1-625delA841907120HC
CAMissensep.G1887Cc.5659G>T841790079NSCLC
CAMissensep.Q710Hc.2130G>T841801364CM
CAMissensep.S1752Ic.5255G>T841790483BRCA
CAMissensep.W1152Lc.3455G>T841792283HNSC
CANonsensep.E877*c.2629G>T841798770LUSC
CASynonymousp.A1452Ac.4356G>T841791382LUAD
C-Frameshiftp.V944Lfs*15c.2830delG841798569HNSC
CGIntronicSNV.c.1482+114G>C841832108HC
CGMissensep.D768Hc.2302G>C841800445BRCA
CGMissensep.E1411Qc.4231G>C841791507HNSC
CGMissensep.E801Qc.2401G>C841800346STAD
CGMissensep.R317Pc.950G>C841836253HNSC
CGMissensep.S842Tc.2525G>C841798874BRCA
CTC-InFrameDeletionp.E993delEc.2977_2979delGAG841798420BLCA
CTC-InFrameDeletionp.E993delEc.2977_2979delGAG841798420THCA
CTMissensep.A1908Tc.5722G>A841790016COREAD
CTMissensep.D1570Nc.4708G>A841791030UCEC
CTMissensep.E1221Kc.3661G>A841792077STAD
CTMissensep.E1405Kc.4213G>A841791525BLCA
CTMissensep.E291Kc.871G>A841838400ESCA
CTMissensep.E924Kc.2770G>A841798629UCEC
CTMissensep.E945Kc.2833G>A841798566UCEC
CTMissensep.G158Dc.473G>A841906023SCLC
CTMissensep.G1974Rc.5920G>A841789818BRCA
CTMissensep.G1980Sc.5938G>A841789800CM
CTMissensep.G78Rc.232G>A841906264CM
CTMissensep.G797Ec.2390G>A841800357CM
CTMissensep.R1169Qc.3506G>A841792232BRCA
CTMissensep.R1877Hc.5630G>A841790108ESCA
CTMissensep.R269Qc.806G>A841839376STAD
CTMissensep.R26Cc.76C>T841906420PAAD
CTMissensep.S1558Nc.4673G>A841791065ESCA
CTMissensep.V585Mc.1753G>A841805418OV
CTMissensep.V786Ic.2356G>A841800391CM
CTNonsensep.W1152*c.3456G>A841792282LUAD
CTSynonymousp.A1476Ac.4428G>A841791310HNSC
CTSynonymousp.E435Ec.1305G>A841834584LUAD
CTSynonymousp.P682Pc.2046G>A841801448STAD
CTSynonymousp.R31Rc.93G>A841906403CM
CTSynonymousp.S525Sc.1575C>T841812837GBM
GAMissensep.A1198Vc.3593C>T841792145COREAD
GAMissensep.A1476Vc.4427C>T841791311COREAD
GAMissensep.A275Vc.824C>T841839358UCEC
GAMissensep.L370Fc.1108C>T841834781LUSC
GAMissensep.P1063Sc.3187C>T841794939CM
GAMissensep.P1196Sc.3586C>T841792152CM
GAMissensep.P1701Lc.5102C>T841790636UCEC
GAMissensep.P1796Sc.5386C>T841790352CM
GAMissensep.P205Lc.614C>T841845068PRAD
GAMissensep.P338Lc.1013C>T841836190PRAD
GAMissensep.P504Lc.1511C>T841812901CM
GAMissensep.P535Sc.1603C>T841806877LUSC
GAMissensep.R329Wc.985C>T841836218RCCC
GAMissensep.R424Wc.1270C>T841834619ESCA
GAMissensep.R748Cc.2242C>T841800505ESCA
GAMissensep.S1194Fc.3581C>T841792157CM
GAMissensep.S1703Lc.5108C>T841790630CM
GAMissensep.S1779Fc.5336C>T841790402CM
GAMissensep.T1009Mc.3026C>T841798373ESCA
GAMissensep.T1455Ic.4364C>T841791374CM
GANonsensep.Q1444*c.4330C>T841791408LUAD
GANonsensep.R357*c.1069C>T841834820CM
GASynonymousp.A908Ac.2724C>T841798675CM
GASynonymousp.F1711Fc.5133C>T841790605BRCA
GASynonymousp.G1742Gc.5226C>T841790512UCEC
GASynonymousp.I1192Ic.3576C>T841792162LUSC
GASynonymousp.I476Ic.1428C>T841832276CM
GASynonymousp.I722Ic.2166C>T841801328CM
GASynonymousp.P1336Pc.4008C>T841791730CM
GASynonymousp.S525Sc.1575C>T841812837CM
GASynonymousp.T1369Tc.4107C>T841791631HNSC
GASynonymousp.T1762Tc.5286C>T841790452LUAD
GCMissensep.L1127Vc.3379C>G841792359BLCA
GCMissensep.L686Vc.2056C>G841801438CM
GCMissensep.P946Ac.2836C>G841798563SCLC
GCMissensep.S729Cc.2186C>G841801308BLCA
GCNonsensep.S378*c.1133C>G841834756ESCA
GCNonsensep.S999*c.2996C>G841798403ESCA
GCNonsensep.S999*c.2996C>G841798403LUSC
GCSynonymousp.L887Lc.2661C>G841798738HNSC
GCSynonymousp.L951Lc.2853C>G841798546CM
GGAAMissensep.P1695Sc.5082_5083delinsTT841790655CM
GTMissensep.F135Lc.405C>A841906091STAD
GTMissensep.P1747Qc.5240C>A841790498CM
GTMissensep.P955Tc.2863C>A841798536STAD
GTMissensep.S1982Yc.5945C>A841789793LUAD
GTSynonymousp.P1220Pc.3660C>A841792078LUAD
GTSynonymousp.P1907Pc.5721C>A841790017CM
GTSynonymousp.S1143Sc.3429C>A841792309CM
GTSynonymousp.S1373Sc.4119C>A841791619CM
TAMissensep.I1855Fc.5563A>T841790175LUSC
TAMissensep.K367Nc.1101A>T841834788CM
TAMissensep.Q1511Lc.4532A>T841791206LUSC
TASpliceAcceptorSNV.c.908-2A>T841836297LUAD
TASynonymousp.T454Tc.1362A>T841834527LUSC
TCMissensep.D1303Gc.3908A>G841791830BRCA
TCMissensep.D1313Gc.3938A>G841791800RCCC
TCMissensep.N397Sc.1190A>G841834699LUSC
TCMissensep.N456Sc.1367A>G841832337OV
TCMissensep.Q1793Rc.5378A>G841790360STAD
TCMissensep.R1082Gc.3244A>G841794882BLCA
TCSynonymousp.E1515Ec.4545A>G841791193MM
TCSynonymousp.L1219Lc.3657A>G841792081HNSC
TGMissensep.E673Dc.2019A>C841801475OV
TGMissensep.K1150Tc.3449A>C841792289RCCC