Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 14 89083213 89083213 + Missense_Mutation SNP C C T TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr14:89083213C>T c.5629G>A c.(5629-5631)Gat>Aat p.D1877N BLCA 14 89109329 89109329 + Missense_Mutation SNP C C G TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr14:89109329C>G c.4121G>C c.(4120-4122)aGa>aCa p.R1374T BLCA 14 89123766 89123766 + Nonsense_Mutation SNP C C A TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr14:89123766C>A c.3958G>T c.(3958-3960)Gga>Tga p.G1320* BLCA 14 89124543 89124543 + Missense_Mutation SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr14:89124543C>T c.3865G>A c.(3865-3867)Gaa>Aaa p.E1289K BLCA 14 89124637 89124637 + Silent SNP G G A TCGA-DK-AA74-01A-11D-A391-08 TCGA-DK-AA74-10A-01D-A394-08 g.chr14:89124637G>A c.3771C>T c.(3769-3771)ggC>ggT p.G1257G BLCA 14 89130890 89130890 + Missense_Mutation SNP C C A TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr14:89130890C>A c.3356G>T c.(3355-3357)gGa>gTa p.G1119V BLCA 14 89131686 89131686 + Missense_Mutation SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr14:89131686G>A c.3272C>T c.(3271-3273)tCa>tTa p.S1091L BLCA 14 89131789 89131789 + Missense_Mutation SNP C C T TCGA-HQ-A2OF-01A-11D-A26M-08 TCGA-HQ-A2OF-10B-01D-A26K-08 g.chr14:89131789C>T c.3169G>A c.(3169-3171)Gta>Ata p.V1057I BLCA 14 89148322 89148322 + Missense_Mutation SNP G G C TCGA-CF-A5UA-01A-11D-A289-08 TCGA-CF-A5UA-10A-01D-A289-08 g.chr14:89148322G>C c.3036C>G c.(3034-3036)atC>atG p.I1012M BLCA 14 89148328 89148328 + Silent SNP C C T TCGA-FJ-A3ZE-01A-11D-A23M-08 TCGA-FJ-A3ZE-10A-01D-A23K-08 g.chr14:89148328C>T c.3030G>A c.(3028-3030)ctG>ctA p.L1010L BLCA 14 89148330 89148330 + Missense_Mutation SNP G G C TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr14:89148330G>C c.3028C>G c.(3028-3030)Ctg>Gtg p.L1010V BLCA 14 89154718 89154718 + Missense_Mutation SNP G G C TCGA-ZF-AA4X-01A-11D-A38G-08 TCGA-ZF-AA4X-10A-01D-A38J-08 g.chr14:89154718G>C c.2639C>G c.(2638-2640)tCt>tGt p.S880C BLCA 14 89168814 89168814 + Missense_Mutation SNP C C G TCGA-DK-A1AB-01A-11D-A13W-08 TCGA-DK-A1AB-10A-01D-A13W-08 g.chr14:89168814C>G c.2214G>C c.(2212-2214)ttG>ttC p.L738F BLCA 14 89171301 89171301 + Nonsense_Mutation SNP G G A TCGA-FD-A62P-01A-32D-A30E-08 TCGA-FD-A62P-10A-01D-A30H-08 g.chr14:89171301G>A c.1954C>T c.(1954-1956)Cag>Tag p.Q652* BLCA 14 89202754 89202754 + Missense_Mutation SNP G G A TCGA-G2-AA3C-01A-21D-A391-08 TCGA-G2-AA3C-10A-01D-A394-08 g.chr14:89202754G>A c.1003C>T c.(1003-1005)Cct>Tct p.P335S BRCA 14 89085011 89085011 + Missense_Mutation SNP C C G TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr14:89085011C>G c.5497G>C c.(5497-5499)Gat>Cat p.D1833H BRCA 14 89091348 89091348 + Missense_Mutation SNP C C T TCGA-E2-A152-01A-11D-A12B-09 TCGA-E2-A152-10A-01D-A12B-09 g.chr14:89091348C>T c.4840G>A c.(4840-4842)Gat>Aat p.D1614N BRCA 14 89091378 89091378 + Missense_Mutation SNP G G A TCGA-BH-A0BZ-01A-31D-A12Q-09 TCGA-BH-A0BZ-11A-61D-A12Q-09 g.chr14:89091378G>A c.4810C>T c.(4810-4812)Cct>Tct p.P1604S BRCA 14 89094085 89094085 + Frame_Shift_Del DEL C C - TCGA-E2-A14Q-01A-11D-A12B-09 TCGA-E2-A14Q-10A-01D-A12B-09 g.chr14:89094085delC c.4412delG c.(4411-4413)ggafs p.G1471fs BRCA 14 89105192 89105192 + Missense_Mutation SNP G G A TCGA-D8-A4Z1-01A-21D-A25Q-09 TCGA-D8-A4Z1-10A-01D-A25Q-09 g.chr14:89105192G>A c.4273C>T c.(4273-4275)Cac>Tac p.H1425Y BRCA 14 89124579 89124579 + Frame_Shift_Del DEL T T - TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr14:89124579delT c.3829delA c.(3829-3831)aggfs p.R1277fs BRCA 14 89153606 89153606 + Silent SNP G G T TCGA-EW-A1OV-01A-11D-A142-09 TCGA-EW-A1OV-10A-01D-A142-09 g.chr14:89153606G>T c.2808C>A c.(2806-2808)ctC>ctA p.L936L BRCA 14 89154694 89154694 + Missense_Mutation SNP C C T TCGA-AQ-A54O-01A-11D-A25Q-09 TCGA-AQ-A54O-10A-01D-A25Q-09 g.chr14:89154694C>T c.2663G>A c.(2662-2664)tGt>tAt p.C888Y BRCA 14 89163200 89163200 + Missense_Mutation SNP C C T TCGA-AR-A5QQ-01A-11D-A28B-09 TCGA-AR-A5QQ-10A-01D-A28E-09 g.chr14:89163200C>T c.2335G>A c.(2335-2337)Gat>Aat p.D779N BRCA 14 89172755 89172755 + Missense_Mutation SNP T T A TCGA-A2-A04N-01A-11D-A10Y-09 TCGA-A2-A04N-10A-01D-A110-09 g.chr14:89172755T>A c.1673A>T c.(1672-1674)aAa>aTa p.K558I BRCA 14 89178714 89178714 + Missense_Mutation SNP C C T TCGA-BH-A0EE-01A-11W-A050-09 TCGA-BH-A0EE-10A-01W-A055-09 g.chr14:89178714C>T c.1558G>A c.(1558-1560)Gat>Aat p.D520N BRCA 14 89202900 89202900 + Missense_Mutation SNP A A G TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr14:89202900A>G c.857T>C c.(856-858)gTa>gCa p.V286A BRCA 14 89205341 89205341 + Missense_Mutation SNP C C T TCGA-BH-A1EN-01A-11D-A17G-09 TCGA-BH-A1EN-11A-23W-A14R-09 g.chr14:89205341C>T c.729G>A c.(727-729)atG>atA p.M243I BRCA 14 89210436 89210436 + Splice_Site SNP C C T TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr14:89210436C>T c.e4-1 BRCA 14 89212617 89212617 + Nonsense_Mutation SNP G G T TCGA-B6-A0IK-01A-12W-A071-09 TCGA-B6-A0IK-10A-01W-A071-09 g.chr14:89212617G>T c.368C>A c.(367-369)tCa>tAa p.S123* CESC 14 89083219 89083219 + Missense_Mutation SNP G G T TCGA-EK-A2RB-01A-11D-A18J-09 TCGA-EK-A2RB-10A-01D-A18J-09 g.chr14:89083219G>T c.5623C>A c.(5623-5625)Cta>Ata p.L1875I CESC 14 89130940 89130940 + Silent SNP G G T TCGA-Q1-A6DV-01A-11D-A32I-09 TCGA-Q1-A6DV-10A-01D-A32I-09 g.chr14:89130940G>T c.3306C>A c.(3304-3306)tcC>tcA p.S1102S CESC 14 89181361 89181361 + Missense_Mutation SNP G G A TCGA-FU-A3HY-01A-11D-A21Q-09 TCGA-FU-A3HY-10A-01D-A21Q-09 g.chr14:89181361G>A c.1366C>T c.(1366-1368)Cat>Tat p.H456Y CHOL 14 89124692 89124692 + Missense_Mutation SNP G G A TCGA-W5-AA30-01A-31D-A417-09 TCGA-W5-AA30-10A-01D-A41A-09 g.chr14:89124692G>A c.3716C>T c.(3715-3717)aCa>aTa p.T1239I CHOL 14 89171303 89171303 + Missense_Mutation SNP G G T TCGA-3X-AAVB-01A-31D-A417-09 TCGA-3X-AAVB-10A-01D-A41A-09 g.chr14:89171303G>T c.1952C>A c.(1951-1953)cCt>cAt p.P651H CHOL 14 89220900 89220900 + Missense_Mutation SNP G G T TCGA-3X-AAV9-01A-72D-A417-09 TCGA-3X-AAV9-10A-01D-A41A-09 g.chr14:89220900G>T c.313C>A c.(313-315)Cat>Aat p.H105N COAD 14 89082533 89082533 + Silent SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr14:89082533A>G c.5826T>C c.(5824-5826)ttT>ttC p.F1942F COAD 14 89082558 89082558 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr14:89082558G>A c.5801C>T c.(5800-5802)tCg>tTg p.S1934L COAD 14 89085018 89085018 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr14:89085018G>T c.5490C>A c.(5488-5490)ttC>ttA p.F1830L COAD 14 89087152 89087152 + Missense_Mutation SNP G G A TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr14:89087152G>A c.5297C>T c.(5296-5298)tCt>tTt p.S1766F COAD 14 89089052 89089054 + In_Frame_Del DEL CTT CTT - TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr14:89089052_89089054delCTT c.4883_4885delAAG c.(4882-4887)gaagga>gga p.E1628del COAD 14 89123739 89123739 + Nonsense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr14:89123739C>A c.3985G>T c.(3985-3987)Gaa>Taa p.E1329* COAD 14 89123777 89123777 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr14:89123777C>T c.3947G>A c.(3946-3948)cGc>cAc p.R1316H COAD 14 89124581 89124581 + Missense_Mutation SNP T T A TCGA-AA-3975-01A-01W-0995-10 TCGA-AA-3975-10A-01W-0999-10 g.chr14:89124581T>A c.3827A>T c.(3826-3828)aAa>aTa p.K1276I COAD 14 89124646 89124646 + Silent SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr14:89124646A>C c.3762T>G c.(3760-3762)gtT>gtG p.V1254V COAD 14 89128020 89128020 + Missense_Mutation SNP T T C TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr14:89128020T>C c.3653A>G c.(3652-3654)aAg>aGg p.K1218R COAD 14 89130896 89130896 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr14:89130896C>T c.3350G>A c.(3349-3351)cGa>cAa p.R1117Q COAD 14 89130933 89130933 + Missense_Mutation SNP T T C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr14:89130933T>C c.3313A>G c.(3313-3315)Agc>Ggc p.S1105G COAD 14 89131804 89131804 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr14:89131804C>T c.3154G>A c.(3154-3156)Ggt>Agt p.G1052S COAD 14 89153603 89153603 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr14:89153603C>A c.2811G>T c.(2809-2811)aaG>aaT p.K937N COAD 14 89172769 89172769 + Splice_Site SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr14:89172769C>T c.1659G>A c.(1657-1659)ggG>ggA p.G553G COAD 14 89178614 89178614 + Splice_Site SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr14:89178614C>T c.e10+1 COAD 14 89192963 89192963 + Missense_Mutation SNP C C T TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr14:89192963C>T c.1109G>A c.(1108-1110)cGt>cAt p.R370H COAD 14 89192995 89192995 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr14:89192995T>G c.1077A>C c.(1075-1077)ttA>ttC p.L359F COAD 14 89202845 89202845 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr14:89202845T>G c.912A>C c.(910-912)gaA>gaC p.E304D COAD 14 89206753 89206753 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr14:89206753C>T c.689G>A c.(688-690)cGa>cAa p.R230Q COAD 14 89206860 89206860 + Silent SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr14:89206860C>T c.582G>A c.(580-582)acG>acA p.T194T COAD 14 89220912 89220912 + Missense_Mutation SNP A A C TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr14:89220912A>C c.301T>G c.(301-303)Tta>Gta p.L101V COADREAD 14 89082533 89082533 + Silent SNP A A G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr14:89082533A>G c.5826T>C c.(5824-5826)ttT>ttC p.F1942F COADREAD 14 89082538 89082538 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:89082538G>A c.5821C>T c.(5821-5823)Cga>Tga p.R1941* COADREAD 14 89082558 89082558 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr14:89082558G>A c.5801C>T c.(5800-5802)tCg>tTg p.S1934L COADREAD 14 89085018 89085018 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr14:89085018G>T c.5490C>A c.(5488-5490)ttC>ttA p.F1830L COADREAD 14 89087152 89087152 + Missense_Mutation SNP G G A TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr14:89087152G>A c.5297C>T c.(5296-5298)tCt>tTt p.S1766F COADREAD 14 89087606 89087606 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:89087606C>T c.5029G>A c.(5029-5031)Gaa>Aaa p.E1677K COADREAD 14 89089052 89089054 + In_Frame_Del DEL CTT CTT - TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr14:89089052_89089054delCTT c.4883_4885delAAG c.(4882-4887)gaagga>gga p.E1628del COADREAD 14 89091350 89091350 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:89091350C>T c.4838G>A c.(4837-4839)cGa>cAa p.R1613Q COADREAD 14 89123739 89123739 + Nonsense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr14:89123739C>A c.3985G>T c.(3985-3987)Gaa>Taa p.E1329* COADREAD 14 89123777 89123777 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr14:89123777C>T c.3947G>A c.(3946-3948)cGc>cAc p.R1316H COADREAD 14 89124581 89124581 + Missense_Mutation SNP T T A TCGA-AA-3975-01A-01W-0995-10 TCGA-AA-3975-10A-01W-0999-10 g.chr14:89124581T>A c.3827A>T c.(3826-3828)aAa>aTa p.K1276I COADREAD 14 89124646 89124646 + Silent SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr14:89124646A>C c.3762T>G c.(3760-3762)gtT>gtG p.V1254V COADREAD 14 89128020 89128020 + Missense_Mutation SNP T T C TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr14:89128020T>C c.3653A>G c.(3652-3654)aAg>aGg p.K1218R COADREAD 14 89130896 89130896 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr14:89130896C>T c.3350G>A c.(3349-3351)cGa>cAa p.R1117Q COADREAD 14 89130933 89130933 + Missense_Mutation SNP T T C TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr14:89130933T>C c.3313A>G c.(3313-3315)Agc>Ggc p.S1105G COADREAD 14 89131804 89131804 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr14:89131804C>T c.3154G>A c.(3154-3156)Ggt>Agt p.G1052S COADREAD 14 89153603 89153603 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr14:89153603C>A c.2811G>T c.(2809-2811)aaG>aaT p.K937N COADREAD 14 89163195 89163195 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:89163195G>A c.2340C>T c.(2338-2340)ttC>ttT p.F780F COADREAD 14 89172769 89172769 + Splice_Site SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr14:89172769C>T c.1659G>A c.(1657-1659)ggG>ggA p.G553G COADREAD 14 89178614 89178614 + Splice_Site SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr14:89178614C>T c.e10+1 COADREAD 14 89192963 89192963 + Missense_Mutation SNP C C T TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr14:89192963C>T c.1109G>A c.(1108-1110)cGt>cAt p.R370H COADREAD 14 89192995 89192995 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr14:89192995T>G c.1077A>C c.(1075-1077)ttA>ttC p.L359F COADREAD 14 89202845 89202845 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr14:89202845T>G c.912A>C c.(910-912)gaA>gaC p.E304D COADREAD 14 89206753 89206753 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr14:89206753C>T c.689G>A c.(688-690)cGa>cAa p.R230Q COADREAD 14 89206860 89206860 + Silent SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr14:89206860C>T c.582G>A c.(580-582)acG>acA p.T194T COADREAD 14 89220912 89220912 + Missense_Mutation SNP A A C TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr14:89220912A>C c.301T>G c.(301-303)Tta>Gta p.L101V DLBC 14 89220874 89220874 + Silent SNP C C T TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr14:89220874C>T c.339G>A c.(337-339)gcG>gcA p.A113A ESCA 14 89082165 89082165 + Missense_Mutation SNP G G T TCGA-L5-A4OF-01A-11D-A27G-09 TCGA-L5-A4OF-11A-12D-A27G-09 g.chr14:89082165G>T c.5907C>A c.(5905-5907)caC>caA p.H1969Q ESCA 14 89124637 89124637 + Silent SNP G G A TCGA-LN-A4A2-01A-31D-A27G-09 TCGA-LN-A4A2-10A-01D-A27G-09 g.chr14:89124637G>A c.3771C>T c.(3769-3771)ggC>ggT p.G1257G ESCA 14 89163272 89163272 + Missense_Mutation SNP T T C TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr14:89163272T>C c.2263A>G c.(2263-2265)Ata>Gta p.I755V ESCA 14 89171240 89171240 + Missense_Mutation SNP G G T TCGA-L5-A8NK-01A-21D-A37C-09 TCGA-L5-A8NK-11A-11D-A37F-09 g.chr14:89171240G>T c.2015C>A c.(2014-2016)gCt>gAt p.A672D ESCA 14 89178750 89178750 + Missense_Mutation SNP C C T TCGA-L5-A8NV-01A-11D-A37C-09 TCGA-L5-A8NV-11A-11D-A37F-09 g.chr14:89178750C>T c.1522G>A c.(1522-1524)Gta>Ata p.V508I ESCA 14 89181397 89181398 + Frame_Shift_Ins INS - - T TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr14:89181397_89181398insT c.1329_1330insA c.(1327-1332)aaagttfs p.V444fs GBM 14 89084607 89084607 + Silent SNP G G A TCGA-06-0644-01A-02D-1492-08 TCGA-06-0644-10A-01D-1492-08 g.chr14:89084607G>A c.5583C>T c.(5581-5583)gcC>gcT p.A1861A GBM 14 89130847 89130847 + Nonsense_Mutation SNP C C T TCGA-76-6285-01A-11D-1696-08 TCGA-76-6285-10A-01D-1696-08 g.chr14:89130847C>T c.3399G>A c.(3397-3399)tgG>tgA p.W1133* GBM 14 89160659 89160659 + Missense_Mutation SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr14:89160659C>T c.2531G>A c.(2530-2532)cGt>cAt p.R844H GBM 14 89168805 89168805 + Silent SNP G G A TCGA-26-5134-01A-01D-1486-08 TCGA-26-5134-10A-01D-1486-08 g.chr14:89168805G>A c.2223C>T c.(2221-2223)taC>taT p.Y741Y GBMLGG 14 89083115 89083115 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr14:89083115G>T c.5727C>A c.(5725-5727)gaC>gaA p.D1909E GBMLGG 14 89084607 89084607 + Silent SNP G G A TCGA-06-0644-01A-02D-1492-08 TCGA-06-0644-10A-01D-1492-08 g.chr14:89084607G>A c.5583C>T c.(5581-5583)gcC>gcT p.A1861A GBMLGG 14 89093251 89093251 + Missense_Mutation SNP G G C TCGA-FG-8191-01A-11D-2253-08 TCGA-FG-8191-10A-01D-2253-08 g.chr14:89093251G>C c.4647C>G c.(4645-4647)agC>agG p.S1549R GBMLGG 14 89130847 89130847 + Nonsense_Mutation SNP C C T TCGA-76-6285-01A-11D-1696-08 TCGA-76-6285-10A-01D-1696-08 g.chr14:89130847C>T c.3399G>A c.(3397-3399)tgG>tgA p.W1133* GBMLGG 14 89154773 89154773 + Missense_Mutation SNP T T C TCGA-HT-8558-01A-21D-2395-08 TCGA-HT-8558-10A-01D-2396-08 g.chr14:89154773T>C c.2584A>G c.(2584-2586)Aaa>Gaa p.K862E GBMLGG 14 89160659 89160659 + Missense_Mutation SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr14:89160659C>T c.2531G>A c.(2530-2532)cGt>cAt p.R844H GBMLGG 14 89160703 89160703 + Silent SNP A A T TCGA-HW-8322-01A-11D-2395-08 TCGA-HW-8322-10A-01D-2396-08 g.chr14:89160703A>T c.2487T>A c.(2485-2487)ccT>ccA p.P829P GBMLGG 14 89168805 89168805 + Silent SNP G G A TCGA-26-5134-01A-01D-1486-08 TCGA-26-5134-10A-01D-1486-08 g.chr14:89168805G>A c.2223C>T c.(2221-2223)taC>taT p.Y741Y HNSC 14 89082514 89082514 + Missense_Mutation SNP C C T TCGA-CQ-6225-01A-11D-1912-08 TCGA-CQ-6225-10A-01D-1912-08 g.chr14:89082514C>T c.5845G>A c.(5845-5847)Gtt>Att p.V1949I HNSC 14 89087643 89087643 + Silent SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr14:89087643G>A c.4992C>T c.(4990-4992)ggC>ggT p.G1664G HNSC 14 89088975 89088975 + Silent SNP A A G TCGA-CV-6960-01A-41D-2012-08 TCGA-CV-6960-10A-01D-2013-08 g.chr14:89088975A>G c.4962T>C c.(4960-4962)gaT>gaC p.D1654D HNSC 14 89091394 89091394 + Silent SNP C C T TCGA-CV-6950-01A-11D-1912-08 TCGA-CV-6950-10A-01D-1912-08 g.chr14:89091394C>T c.4794G>A c.(4792-4794)gcG>gcA p.A1598A HNSC 14 89093259 89093259 + Missense_Mutation SNP G G C TCGA-D6-A4ZB-01A-11D-A25D-08 TCGA-D6-A4ZB-10A-01D-A25E-08 g.chr14:89093259G>C c.4639C>G c.(4639-4641)Ctt>Gtt p.L1547V HNSC 14 89124669 89124669 + Missense_Mutation SNP T T A TCGA-CV-A45R-01A-11D-A24D-08 TCGA-CV-A45R-10A-01D-A24F-08 g.chr14:89124669T>A c.3739A>T c.(3739-3741)Act>Tct p.T1247S HNSC 14 89124674 89124674 + Missense_Mutation SNP C C T TCGA-CQ-6219-01A-11D-1912-08 TCGA-CQ-6219-10A-01D-1912-08 g.chr14:89124674C>T c.3734G>A c.(3733-3735)cGc>cAc p.R1245H HNSC 14 89130941 89130941 + Missense_Mutation SNP G G C TCGA-CR-7397-01A-11D-2012-08 TCGA-CR-7397-10A-01D-2013-08 g.chr14:89130941G>C c.3305C>G c.(3304-3306)tCc>tGc p.S1102C HNSC 14 89131807 89131807 + Missense_Mutation SNP C C T TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr14:89131807C>T c.3151G>A c.(3151-3153)Gat>Aat p.D1051N HNSC 14 89192964 89192964 + Missense_Mutation SNP G G C TCGA-BB-4227-01A-01D-1870-08 TCGA-BB-4227-10A-01D-1870-08 g.chr14:89192964G>C c.1108C>G c.(1108-1110)Cgt>Ggt p.R370G HNSC 14 89202827 89202827 + Silent SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr14:89202827C>T c.930G>A c.(928-930)gtG>gtA p.V310V HNSC 14 89206756 89206756 + Missense_Mutation SNP A A G TCGA-CQ-6222-01A-11D-1912-08 TCGA-CQ-6222-10A-01D-1912-08 g.chr14:89206756A>G c.686T>C c.(685-687)aTa>aCa p.I229T KIPAN 14 89093186 89093186 + Missense_Mutation SNP C C T TCGA-B8-5549-01A-01D-1534-10 TCGA-B8-5549-10A-01D-1535-10 g.chr14:89093186C>T c.4712G>A c.(4711-4713)gGt>gAt p.G1571D KIPAN 14 89093338 89093338 + Missense_Mutation SNP T T G TCGA-4A-A93X-01A-11D-A36X-10 TCGA-4A-A93X-10A-01D-A370-10 g.chr14:89093338T>G c.4560A>C c.(4558-4560)gaA>gaC p.E1520D KIPAN 14 89105224 89105224 + Missense_Mutation SNP T T G TCGA-GL-A4EM-01A-11D-A25F-10 TCGA-GL-A4EM-10A-01D-A25F-10 g.chr14:89105224T>G c.4241A>C c.(4240-4242)aAt>aCt p.N1414T KIPAN 14 89109293 89109293 + Missense_Mutation SNP C C T TCGA-MH-A857-01A-11D-A34Z-10 TCGA-MH-A857-10A-01D-A34Z-10 g.chr14:89109293C>T c.4157G>A c.(4156-4158)gGt>gAt p.G1386D KIPAN 14 89128042 89128042 + Missense_Mutation SNP C C A TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr14:89128042C>A c.3631G>T c.(3631-3633)Ggg>Tgg p.G1211W KIPAN 14 89128141 89128141 + Missense_Mutation SNP C C A TCGA-CZ-4857-01A-01D-1373-10 TCGA-CZ-4857-11A-01D-1373-10 g.chr14:89128141C>A c.3532G>T c.(3532-3534)Gta>Tta p.V1178L KIPAN 14 89153576 89153576 + Silent SNP C C T TCGA-BP-4795-01A-02D-1421-08 TCGA-BP-4795-11A-01D-1421-08 g.chr14:89153576C>T c.2838G>A c.(2836-2838)ttG>ttA p.L946L KIPAN 14 89161727 89161727 + Missense_Mutation SNP C C T TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr14:89161727C>T c.2416G>A c.(2416-2418)Gga>Aga p.G806R KIPAN 14 89168918 89168919 + Missense_Mutation DNP AC AC TG TCGA-B0-5701-01A-11D-1534-10 TCGA-B0-5701-11A-01D-1534-10 g.chr14:89168918_89168919AC>TG c.2109_2110GT>CA c.(2107-2112)gtGTac>gtCAac p.Y704N KIPAN 14 89171882 89171883 + Frame_Shift_Ins INS - - T TCGA-GL-A59R-01A-11D-A26P-10 TCGA-GL-A59R-10A-01D-A26P-10 g.chr14:89171882_89171883insT c.1875_1876insA c.(1873-1878)gatgttfs p.V626fs KIPAN 14 89202708 89202708 + Splice_Site SNP C C G TCGA-CJ-4920-01A-01D-1429-08 TCGA-CJ-4920-11A-01D-1429-08 g.chr14:89202708C>G c.1049G>C c.(1048-1050)aGg>aCg p.R350T KIRC 14 89093186 89093186 + Missense_Mutation SNP C C T TCGA-B8-5549-01A-01D-1534-10 TCGA-B8-5549-10A-01D-1535-10 g.chr14:89093186C>T c.4712G>A c.(4711-4713)gGt>gAt p.G1571D KIRC 14 89128141 89128141 + Missense_Mutation SNP C C A TCGA-CZ-4857-01A-01D-1373-10 TCGA-CZ-4857-11A-01D-1373-10 g.chr14:89128141C>A c.3532G>T c.(3532-3534)Gta>Tta p.V1178L KIRC 14 89153576 89153576 + Silent SNP C C T TCGA-BP-4795-01A-02D-1421-08 TCGA-BP-4795-11A-01D-1421-08 g.chr14:89153576C>T c.2838G>A c.(2836-2838)ttG>ttA p.L946L KIRC 14 89168918 89168919 + Missense_Mutation DNP AC AC TG TCGA-B0-5701-01A-11D-1534-10 TCGA-B0-5701-11A-01D-1534-10 g.chr14:89168918_89168919AC>TG c.2109_2110GT>CA c.(2107-2112)gtGTac>gtCAac p.Y704N KIRC 14 89202708 89202708 + Splice_Site SNP C C G TCGA-CJ-4920-01A-01D-1429-08 TCGA-CJ-4920-11A-01D-1429-08 g.chr14:89202708C>G c.1049G>C c.(1048-1050)aGg>aCg p.R350T KIRP 14 89093338 89093338 + Missense_Mutation SNP T T G TCGA-4A-A93X-01A-11D-A36X-10 TCGA-4A-A93X-10A-01D-A370-10 g.chr14:89093338T>G c.4560A>C c.(4558-4560)gaA>gaC p.E1520D KIRP 14 89105224 89105224 + Missense_Mutation SNP T T G TCGA-GL-A4EM-01A-11D-A25F-10 TCGA-GL-A4EM-10A-01D-A25F-10 g.chr14:89105224T>G c.4241A>C c.(4240-4242)aAt>aCt p.N1414T KIRP 14 89109293 89109293 + Missense_Mutation SNP C C T TCGA-MH-A857-01A-11D-A34Z-10 TCGA-MH-A857-10A-01D-A34Z-10 g.chr14:89109293C>T c.4157G>A c.(4156-4158)gGt>gAt p.G1386D KIRP 14 89128042 89128042 + Missense_Mutation SNP C C A TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr14:89128042C>A c.3631G>T c.(3631-3633)Ggg>Tgg p.G1211W KIRP 14 89161727 89161727 + Missense_Mutation SNP C C T TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr14:89161727C>T c.2416G>A c.(2416-2418)Gga>Aga p.G806R KIRP 14 89171882 89171883 + Frame_Shift_Ins INS - - T TCGA-GL-A59R-01A-11D-A26P-10 TCGA-GL-A59R-10A-01D-A26P-10 g.chr14:89171882_89171883insT c.1875_1876insA c.(1873-1878)gatgttfs p.V626fs LGG 14 89083115 89083115 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr14:89083115G>T c.5727C>A c.(5725-5727)gaC>gaA p.D1909E LGG 14 89093251 89093251 + Missense_Mutation SNP G G C TCGA-FG-8191-01A-11D-2253-08 TCGA-FG-8191-10A-01D-2253-08 g.chr14:89093251G>C c.4647C>G c.(4645-4647)agC>agG p.S1549R LGG 14 89154773 89154773 + Missense_Mutation SNP T T C TCGA-HT-8558-01A-21D-2395-08 TCGA-HT-8558-10A-01D-2396-08 g.chr14:89154773T>C c.2584A>G c.(2584-2586)Aaa>Gaa p.K862E LGG 14 89160703 89160703 + Silent SNP A A T TCGA-HW-8322-01A-11D-2395-08 TCGA-HW-8322-10A-01D-2396-08 g.chr14:89160703A>T c.2487T>A c.(2485-2487)ccT>ccA p.P829P LIHC 14 89087164 89087164 + Frame_Shift_Del DEL A A - TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr14:89087164delA c.5285delT c.(5284-5286)ttafs p.L1763fs LIHC 14 89094074 89094074 + Missense_Mutation SNP C C A TCGA-DD-AADA-01A-11D-A40R-10 TCGA-DD-AADA-10A-01D-A40U-10 g.chr14:89094074C>A c.4423G>T c.(4423-4425)Gtc>Ttc p.V1475F LIHC 14 89105158 89105158 + Missense_Mutation SNP T T A TCGA-DD-AACL-01A-11D-A40R-10 TCGA-DD-AACL-10A-01D-A40U-10 g.chr14:89105158T>A c.4307A>T c.(4306-4308)cAa>cTa p.Q1436L LIHC 14 89153622 89153622 + Missense_Mutation SNP G G T TCGA-2V-A95S-01A-11D-A36X-10 TCGA-2V-A95S-10D-01D-A370-10 g.chr14:89153622G>T c.2792C>A c.(2791-2793)tCt>tAt p.S931Y LIHC 14 89154769 89154769 + Frame_Shift_Del DEL T T - TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr14:89154769delT c.2588delA c.(2587-2589)aatfs p.N863fs LIHC 14 89172628 89172628 + Silent SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr14:89172628T>C c.1800A>G c.(1798-1800)aaA>aaG p.K600K LIHC 14 89202777 89202777 + Missense_Mutation SNP T T A TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chr14:89202777T>A c.980A>T c.(979-981)gAa>gTa p.E327V LIHC 14 89202828 89202828 + Missense_Mutation SNP A A G TCGA-DD-AAE1-01A-11D-A40R-10 TCGA-DD-AAE1-10A-01D-A40U-10 g.chr14:89202828A>G c.929T>C c.(928-930)gTg>gCg p.V310A LIHC 14 89206879 89206879 + Missense_Mutation SNP C C T TCGA-BW-A5NQ-01A-11D-A27I-10 TCGA-BW-A5NQ-10A-01D-A27I-10 g.chr14:89206879C>T c.563G>A c.(562-564)cGa>cAa p.R188Q LIHC 14 89206909 89206909 + Missense_Mutation SNP C C T TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr14:89206909C>T c.533G>A c.(532-534)aGt>aAt p.S178N LIHC 14 89258735 89258735 + Missense_Mutation SNP T T A TCGA-DD-AACZ-01A-11D-A40R-10 TCGA-DD-AACZ-10A-01D-A40U-10 g.chr14:89258735T>A c.113A>T c.(112-114)tAc>tTc p.Y38F LUAD 14 89087598 89087599 + Frame_Shift_Ins INS - - C TCGA-05-4250-01A-01D-1105-08 TCGA-05-4250-10A-01D-1105-08 g.chr14:89087598_89087599insC c.5036_5037insG c.(5035-5037)ggafs p.G1679fs LUAD 14 89087624 89087624 + Silent SNP T T G TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chr14:89087624T>G c.5011A>C c.(5011-5013)Agg>Cgg p.R1671R LUAD 14 89091321 89091321 + Missense_Mutation SNP C C G TCGA-53-7626-01A-12D-2063-08 TCGA-53-7626-10A-01D-2063-08 g.chr14:89091321C>G c.4867G>C c.(4867-4869)Gaa>Caa p.E1623Q LUAD 14 89093342 89093342 + Missense_Mutation SNP G G T TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr14:89093342G>T c.4556C>A c.(4555-4557)gCa>gAa p.A1519E LUAD 14 89109347 89109347 + Missense_Mutation SNP A A C TCGA-55-8301-01A-11D-2284-08 TCGA-55-8301-10A-01D-2284-08 g.chr14:89109347A>C c.4103T>G c.(4102-4104)aTt>aGt p.I1368S LUAD 14 89124732 89124732 + Splice_Site SNP C C A TCGA-53-A4EZ-01A-12D-A24P-08 TCGA-53-A4EZ-10A-01D-A24P-08 g.chr14:89124732C>A c.3676G>T c.(3676-3678)Ggg>Tgg p.G1226W LUAD 14 89128042 89128042 + Missense_Mutation SNP C C A TCGA-MP-A4T9-01A-11D-A24P-08 TCGA-MP-A4T9-10A-01D-A24P-08 g.chr14:89128042C>A c.3631G>T c.(3631-3633)Ggg>Tgg p.G1211W LUAD 14 89154817 89154817 + Splice_Site SNP C C A TCGA-50-5066-01A-01D-1625-08 TCGA-50-5066-10A-01D-1625-08 g.chr14:89154817C>A c.2540G>T c.(2539-2541)gGg>gTg p.G847V LUAD 14 89161767 89161767 + Silent SNP T T A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr14:89161767T>A c.2376A>T c.(2374-2376)atA>atT p.I792I LUAD 14 89163230 89163230 + Missense_Mutation SNP C C A TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr14:89163230C>A c.2305G>T c.(2305-2307)Ggc>Tgc p.G769C LUAD 14 89163292 89163292 + Missense_Mutation SNP C C G TCGA-MP-A4TE-01A-22D-A25L-08 TCGA-MP-A4TE-10A-01D-A25L-08 g.chr14:89163292C>G c.2243G>C c.(2242-2244)gGt>gCt p.G748A LUAD 14 89168855 89168855 + Missense_Mutation SNP C C A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr14:89168855C>A c.2173G>T c.(2173-2175)Ggt>Tgt p.G725C LUAD 14 89181356 89181356 + Silent SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr14:89181356C>A c.1371G>T c.(1369-1371)ctG>ctT p.L457L LUAD 14 89181381 89181381 + Frame_Shift_Del DEL C C - TCGA-91-6831-01A-11D-1855-08 TCGA-91-6831-11A-02D-1855-08 g.chr14:89181381delC c.1346delG c.(1345-1347)ggafs p.G449fs LUAD 14 89181511 89181511 + Missense_Mutation SNP C C A TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr14:89181511C>A c.1216G>T c.(1216-1218)Gat>Tat p.D406Y LUAD 14 89202855 89202855 + Missense_Mutation SNP T T A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr14:89202855T>A c.902A>T c.(901-903)cAg>cTg p.Q301L LUAD 14 89205241 89205241 + Missense_Mutation SNP T T C TCGA-78-7159-01A-11D-2036-08 TCGA-78-7159-10A-01D-2036-08 g.chr14:89205241T>C c.829A>G c.(829-831)Aca>Gca p.T277A LUAD 14 89205259 89205259 + Missense_Mutation SNP C C A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr14:89205259C>A c.811G>T c.(811-813)Gtg>Ttg p.V271L LUAD 14 89206766 89206766 + Missense_Mutation SNP T T C TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr14:89206766T>C c.676A>G c.(676-678)Atc>Gtc p.I226V LUAD 14 89220988 89220988 + Silent SNP C C T TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr14:89220988C>T c.225G>A c.(223-225)ttG>ttA p.L75L LUSC 14 89087225 89087225 + Missense_Mutation SNP A A G TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr14:89087225A>G c.5224T>C c.(5224-5226)Tgt>Cgt p.C1742R LUSC 14 89105221 89105221 + Missense_Mutation SNP T T C TCGA-43-5668-01A-01D-1632-08 TCGA-43-5668-11A-01D-1632-08 g.chr14:89105221T>C c.4244A>G c.(4243-4245)gAt>gGt p.D1415G LUSC 14 89123748 89123748 + Nonsense_Mutation SNP G G A TCGA-60-2713-01A-01D-1522-08 TCGA-60-2713-11A-01D-1522-08 g.chr14:89123748G>A c.3976C>T c.(3976-3978)Caa>Taa p.Q1326* LUSC 14 89154734 89154734 + Missense_Mutation SNP C C T TCGA-21-1071-01A-01D-1521-08 TCGA-21-1071-11A-01D-1521-08 g.chr14:89154734C>T c.2623G>A c.(2623-2625)Gaa>Aaa p.E875K LUSC 14 89163203 89163203 + Missense_Mutation SNP C C A TCGA-33-4586-01A-01D-1441-08 TCGA-33-4586-11A-01D-1441-08 g.chr14:89163203C>A c.2332G>T c.(2332-2334)Gtt>Ttt p.V778F LUSC 14 89168804 89168804 + Missense_Mutation SNP C C G TCGA-18-4721-01A-01D-1441-08 TCGA-18-4721-11A-01D-1441-08 g.chr14:89168804C>G c.2224G>C c.(2224-2226)Gtg>Ctg p.V742L LUSC 14 89181371 89181371 + Silent SNP A A G TCGA-60-2726-01A-01D-1522-08 TCGA-60-2726-11A-01D-1522-08 g.chr14:89181371A>G c.1356T>C c.(1354-1356)agT>agC p.S452S LUSC 14 89181377 89181377 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr14:89181377G>A c.1350C>T c.(1348-1350)tcC>tcT p.S450S LUSC 14 89192897 89192897 + Missense_Mutation SNP A A G TCGA-18-5592-01A-01D-1632-08 TCGA-18-5592-11A-11D-1632-08 g.chr14:89192897A>G c.1175T>C c.(1174-1176)gTa>gCa p.V392A LUSC 14 89202760 89202760 + Missense_Mutation SNP C C A TCGA-22-5482-01A-01D-1632-08 TCGA-22-5482-11A-01D-1632-08 g.chr14:89202760C>A c.997G>T c.(997-999)Gtc>Ttc p.V333F OV 14 89129375 89129375 + Splice_Site SNP C C T TCGA-24-1431-01A-01D-0472-08 TCGA-24-1431-10A-01D-0472-08 g.chr14:89129375C>T c.3498G>A c.(3496-3498)gaG>gaA p.E1166E OV 14 89151472 89151472 + Missense_Mutation SNP C C A TCGA-24-1604-01A-01W-0552-10 TCGA-24-1604-10A-01W-0552-10 g.chr14:89151472C>A c.2869G>T c.(2869-2871)Gat>Tat p.D957Y OV 14 89205266 89205266 + Silent SNP T T C TCGA-13-1509-01A-01W-0549-09 TCGA-13-1509-10A-01W-0550-09 g.chr14:89205266T>C c.804A>G c.(802-804)ccA>ccG p.P268P PAAD 14 89083140 89083140 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:89083140C>T c.5702G>A c.(5701-5703)gGa>gAa p.G1901E PAAD 14 89171223 89171223 + Nonsense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:89171223G>A c.2032C>T c.(2032-2034)Cga>Tga p.R678* PCPG 14 89206879 89206879 + Missense_Mutation SNP C C T TCGA-RW-A68D-01A-11D-A35D-08 TCGA-RW-A68D-10A-01D-A35B-08 g.chr14:89206879C>T c.563G>A c.(562-564)cGa>cAa p.R188Q PRAD 14 89083083 89083083 + Missense_Mutation SNP C C T TCGA-EJ-5503-01A-01D-1576-08 TCGA-EJ-5503-10A-01D-1577-08 g.chr14:89083083C>T c.5759G>A c.(5758-5760)tGt>tAt p.C1920Y PRAD 14 89148373 89148373 + Silent SNP T T C TCGA-KK-A8IJ-01A-11D-A34U-08 TCGA-KK-A8IJ-11A-11D-A34X-08 g.chr14:89148373T>C c.2985A>G c.(2983-2985)ggA>ggG p.G995G PRAD 14 89154654 89154654 + Silent SNP C C T TCGA-ZG-A9L6-01A-11D-A41K-08 TCGA-ZG-A9L6-10A-01D-A41N-08 g.chr14:89154654C>T c.2703G>A c.(2701-2703)gcG>gcA p.A901A PRAD 14 89168815 89168815 + Missense_Mutation SNP A A G TCGA-EJ-5518-01A-01D-1576-08 TCGA-EJ-5518-10A-01D-1577-08 g.chr14:89168815A>G c.2213T>C c.(2212-2214)tTg>tCg p.L738S READ 14 89082538 89082538 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:89082538G>A c.5821C>T c.(5821-5823)Cga>Tga p.R1941* READ 14 89087606 89087606 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:89087606C>T c.5029G>A c.(5029-5031)Gaa>Aaa p.E1677K READ 14 89091350 89091350 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:89091350C>T c.4838G>A c.(4837-4839)cGa>cAa p.R1613Q READ 14 89163195 89163195 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:89163195G>A c.2340C>T c.(2338-2340)ttC>ttT p.F780F SARC 14 89110777 89110777 + Splice_Site SNP C C A TCGA-X6-A7W8-01A-21D-A351-09 TCGA-X6-A7W8-10A-01D-A351-09 g.chr14:89110777C>A c.4083G>T c.(4081-4083)gaG>gaT p.E1361D SARC 14 89168805 89168805 + Silent SNP G G A TCGA-DX-A23U-01A-11D-A26G-09 TCGA-DX-A23U-10A-01D-A26G-09 g.chr14:89168805G>A c.2223C>T c.(2221-2223)taC>taT p.Y741Y SARC 14 89202819 89202819 + Missense_Mutation SNP C C T TCGA-QQ-A8VG-01A-11D-A37C-09 TCGA-QQ-A8VG-10A-01D-A37F-09 g.chr14:89202819C>T c.938G>A c.(937-939)aGa>aAa p.R313K SARC 14 89202895 89202895 + Missense_Mutation SNP T T A TCGA-FX-A3RE-01A-11D-A228-09 TCGA-FX-A3RE-10A-01D-A22A-09 g.chr14:89202895T>A c.862A>T c.(862-864)Agt>Tgt p.S288C SKCM 14 89083224 89083224 + Splice_Site SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr14:89083224C>T c.e40-1 SKCM 14 89091324 89091324 + Nonsense_Mutation SNP T T A TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr14:89091324T>A c.4864A>T c.(4864-4866)Aag>Tag p.K1622* SKCM 14 89093244 89093244 + Missense_Mutation SNP C C T TCGA-EE-A2MU-06A-21D-A196-08 TCGA-EE-A2MU-10A-01D-A198-08 g.chr14:89093244C>T c.4654G>A c.(4654-4656)Ggg>Agg p.G1552R SKCM 14 89093316 89093316 + Missense_Mutation SNP G G C TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr14:89093316G>C c.4582C>G c.(4582-4584)Cag>Gag p.Q1528E SKCM 14 89093343 89093343 + Missense_Mutation SNP C C T TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr14:89093343C>T c.4555G>A c.(4555-4557)Gca>Aca p.A1519T SKCM 14 89094155 89094155 + Missense_Mutation SNP G G A TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr14:89094155G>A c.4342C>T c.(4342-4344)Cct>Tct p.P1448S SKCM 14 89109309 89109309 + Missense_Mutation SNP G G A TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr14:89109309G>A c.4141C>T c.(4141-4143)Cac>Tac p.H1381Y SKCM 14 89123778 89123778 + Missense_Mutation SNP G G A TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr14:89123778G>A c.3946C>T c.(3946-3948)Cgc>Tgc p.R1316C SKCM 14 89124642 89124642 + Missense_Mutation SNP G G C TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr14:89124642G>C c.3766C>G c.(3766-3768)Cta>Gta p.L1256V SKCM 14 89131692 89131692 + Missense_Mutation SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr14:89131692C>T c.3266G>A c.(3265-3267)cGa>cAa p.R1089Q SKCM 14 89131701 89131701 + Missense_Mutation SNP G G A TCGA-FS-A1ZD-06A-11D-A197-08 TCGA-FS-A1ZD-10A-01D-A199-08 g.chr14:89131701G>A c.3257C>T c.(3256-3258)tCa>tTa p.S1086L SKCM 14 89148295 89148295 + Silent SNP G G A TCGA-EE-A2MF-06A-11D-A21A-08 TCGA-EE-A2MF-10B-01D-A21A-08 g.chr14:89148295G>A c.3063C>T c.(3061-3063)acC>acT p.T1021T SKCM 14 89151388 89151388 + Missense_Mutation SNP T T C TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr14:89151388T>C c.2953A>G c.(2953-2955)Aaa>Gaa p.K985E SKCM 14 89153569 89153569 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr14:89153569C>T c.2845G>A c.(2845-2847)Gga>Aga p.G949R SKCM 14 89154722 89154722 + Missense_Mutation SNP A A C TCGA-D3-A3MU-06A-11D-A21A-08 TCGA-D3-A3MU-10A-01D-A21A-08 g.chr14:89154722A>C c.2635T>G c.(2635-2637)Ttt>Gtt p.F879V SKCM 14 89154729 89154729 + Silent SNP C C T TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr14:89154729C>T c.2628G>A c.(2626-2628)gaG>gaA p.E876E SKCM 14 89163205 89163205 + Missense_Mutation SNP G G A TCGA-EE-A2A5-06A-11D-A197-08 TCGA-EE-A2A5-10A-01D-A199-08 g.chr14:89163205G>A c.2330C>T c.(2329-2331)gCc>gTc p.A777V SKCM 14 89168884 89168884 + Missense_Mutation SNP C C T TCGA-FW-A3TV-06A-11D-A23B-08 TCGA-FW-A3TV-10A-01D-A23B-08 g.chr14:89168884C>T c.2144G>A c.(2143-2145)cGa>cAa p.R715Q SKCM 14 89171280 89171280 + Missense_Mutation SNP C C T TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr14:89171280C>T c.1975G>A c.(1975-1977)Gag>Aag p.E659K SKCM 14 89172638 89172638 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr14:89172638C>T c.1790G>A c.(1789-1791)aGa>aAa p.R597K SKCM 14 89178744 89178744 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr14:89178744C>T c.1528G>A c.(1528-1530)Gga>Aga p.G510R SKCM 14 89178746 89178746 + Missense_Mutation SNP T T A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr14:89178746T>A c.1526A>T c.(1525-1527)aAt>aTt p.N509I SKCM 14 89181355 89181355 + Missense_Mutation SNP C C T TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr14:89181355C>T c.1372G>A c.(1372-1374)Gac>Aac p.D458N SKCM 14 89181462 89181462 + Missense_Mutation SNP T T A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr14:89181462T>A c.1265A>T c.(1264-1266)tAc>tTc p.Y422F SKCM 14 89202718 89202718 + Missense_Mutation SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr14:89202718G>A c.1039C>T c.(1039-1041)Cgt>Tgt p.R347C SKCM 14 89202745 89202745 + Missense_Mutation SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr14:89202745G>A c.1012C>T c.(1012-1014)Cct>Tct p.P338S SKCM 14 89202882 89202882 + Missense_Mutation SNP C C T TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr14:89202882C>T c.875G>A c.(874-876)cGa>cAa p.R292Q SKCM 14 89206788 89206788 + Silent SNP C C T TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chr14:89206788C>T c.654G>A c.(652-654)ggG>ggA p.G218G SKCM 14 89206850 89206850 + Nonsense_Mutation SNP G G A TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr14:89206850G>A c.592C>T c.(592-594)Cag>Tag p.Q198* SKCM 14 89206879 89206879 + Missense_Mutation SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr14:89206879C>T c.563G>A c.(562-564)cGa>cAa p.R188Q SKCM 14 89220907 89220907 + Silent SNP C C T TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr14:89220907C>T c.306G>A c.(304-306)aaG>aaA p.K102K

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 14 89109329 89109329 single base substitution C G 3_prime_UTR_variant BLCA-US 14 89109329 89109329 single base substitution C G exon_variant BLCA-US 14 89109329 89109329 single base substitution C G missense_variant R1336T 4007G>C BLCA-US 14 89109329 89109329 single base substitution C G missense_variant R1374T 4121G>C BLCA-US 14 89109329 89109329 single base substitution C G missense_variant R1382T 4145G>C BLCA-US 14 89124543 89124543 single base substitution C T 3_prime_UTR_variant BLCA-US 14 89124543 89124543 single base substitution C T missense_variant E1251K 3751G>A BLCA-US 14 89124543 89124543 single base substitution C T missense_variant E1289K 3865G>A BLCA-US 14 89131686 89131686 single base substitution G A 3_prime_UTR_variant BLCA-US 14 89131686 89131686 single base substitution G A exon_variant BLCA-US 14 89131686 89131686 single base substitution G A missense_variant S1053L 3158C>T BLCA-US 14 89131686 89131686 single base substitution G A missense_variant S1091L 3272C>T BLCA-US 14 89148328 89148328 single base substitution C T 3_prime_UTR_variant BLCA-US 14 89148328 89148328 single base substitution C T synonymous_variant L1010L 3030G>A BLCA-US 14 89148328 89148328 single base substitution C T synonymous_variant L972L 2916G>A BLCA-US 14 89168814 89168814 single base substitution C G 3_prime_UTR_variant BLCA-US 14 89168814 89168814 single base substitution C G missense_variant L738F 2214G>C BOCA-FR 14 89077836 89077836 single base substitution C T downstream_gene_variant BOCA-FR 14 89172481 89172481 single base substitution C A intron_variant BRCA-EU 14 89074691 89074691 single base substitution T A downstream_gene_variant BRCA-EU 14 89075647 89075647 single base substitution G A downstream_gene_variant BRCA-EU 14 89076117 89076117 single base substitution G A downstream_gene_variant BRCA-EU 14 89078667 89078667 single base substitution C G downstream_gene_variant BRCA-EU 14 89078774 89078774 single base substitution A G downstream_gene_variant BRCA-EU 14 89079317 89079317 single base substitution A T 3_prime_UTR_variant BRCA-EU 14 89079317 89079317 single base substitution A T downstream_gene_variant BRCA-EU 14 89084283 89084283 single base substitution T C downstream_gene_variant BRCA-EU 14 89084283 89084283 single base substitution T C intron_variant BRCA-EU 14 89084914 89084914 single base substitution G T downstream_gene_variant BRCA-EU 14 89084914 89084914 single base substitution G T intron_variant BRCA-EU 14 89087180 89087180 single base substitution C G 3_prime_UTR_variant BRCA-EU 14 89087180 89087180 single base substitution C G downstream_gene_variant BRCA-EU 14 89087180 89087180 single base substitution C G missense_variant G1719R 5155G>C BRCA-EU 14 89087180 89087180 single base substitution C G missense_variant G1757R 5269G>C BRCA-EU 14 89087180 89087180 single base substitution C G missense_variant G1765R 5293G>C BRCA-EU 14 89087180 89087180 single base substitution C G missense_variant G205R 613G>C BRCA-EU 14 89087180 89087180 single base substitution C G upstream_gene_variant BRCA-EU 14 89087450 89087450 insertion of <=200bp - TAC downstream_gene_variant BRCA-EU 14 89087450 89087450 insertion of <=200bp - TAC splice_region_variant BRCA-EU 14 89087450 89087450 insertion of <=200bp - TAC upstream_gene_variant BRCA-EU 14 89088088 89088088 single base substitution G A downstream_gene_variant BRCA-EU 14 89088088 89088088 single base substitution G A intron_variant BRCA-EU 14 89088088 89088088 single base substitution G A upstream_gene_variant BRCA-EU 14 89088210 89088210 single base substitution T G 3_prime_UTR_variant BRCA-EU 14 89088210 89088210 single base substitution T G intron_variant BRCA-EU 14 89088210 89088210 single base substitution T G upstream_gene_variant BRCA-EU 14 89088737 89088737 single base substitution A G intron_variant BRCA-EU 14 89088737 89088737 single base substitution A G upstream_gene_variant BRCA-EU 14 89089612 89089612 single base substitution C T downstream_gene_variant BRCA-EU 14 89089612 89089612 single base substitution C T intron_variant BRCA-EU 14 89089612 89089612 single base substitution C T upstream_gene_variant BRCA-EU 14 89089718 89089718 single base substitution G A downstream_gene_variant BRCA-EU 14 89089718 89089718 single base substitution G A intron_variant BRCA-EU 14 89089718 89089718 single base substitution G A upstream_gene_variant BRCA-EU 14 89089847 89089847 single base substitution C T downstream_gene_variant BRCA-EU 14 89089847 89089847 single base substitution C T intron_variant BRCA-EU 14 89089847 89089847 single base substitution C T upstream_gene_variant BRCA-EU 14 89090367 89090367 single base substitution C G downstream_gene_variant BRCA-EU 14 89090367 89090367 single base substitution C G intron_variant BRCA-EU 14 89090367 89090367 single base substitution C G upstream_gene_variant BRCA-EU 14 89090809 89090809 single base substitution C G downstream_gene_variant BRCA-EU 14 89090809 89090809 single base substitution C G intron_variant BRCA-EU 14 89090809 89090809 single base substitution C G upstream_gene_variant BRCA-EU 14 89090904 89090904 single base substitution C T downstream_gene_variant BRCA-EU 14 89090904 89090904 single base substitution C T intron_variant BRCA-EU 14 89090904 89090904 single base substitution C T upstream_gene_variant BRCA-EU 14 89090913 89090913 single base substitution C T downstream_gene_variant BRCA-EU 14 89090913 89090913 single base substitution C T intron_variant BRCA-EU 14 89090913 89090913 single base substitution C T upstream_gene_variant BRCA-EU 14 89091820 89091820 single base substitution A G downstream_gene_variant BRCA-EU 14 89091820 89091820 single base substitution A G intron_variant BRCA-EU 14 89092676 89092676 single base substitution C A downstream_gene_variant BRCA-EU 14 89092676 89092676 single base substitution C A intron_variant BRCA-EU 14 89096729 89096729 single base substitution G C intron_variant BRCA-EU 14 89096729 89096729 single base substitution G C upstream_gene_variant BRCA-EU 14 89099072 89099072 single base substitution C G intron_variant BRCA-EU 14 89099721 89099721 single base substitution G T intron_variant BRCA-EU 14 89100138 89100138 single base substitution G C intron_variant BRCA-EU 14 89100681 89100681 single base substitution C T intron_variant BRCA-EU 14 89101215 89101215 single base substitution G A intron_variant BRCA-EU 14 89101317 89101317 single base substitution G C intron_variant BRCA-EU 14 89101351 89101351 single base substitution G A intron_variant BRCA-EU 14 89101496 89101496 single base substitution C G intron_variant BRCA-EU 14 89102591 89102591 single base substitution C T intron_variant BRCA-EU 14 89102656 89102656 single base substitution C G intron_variant BRCA-EU 14 89104457 89104457 single base substitution A G intron_variant BRCA-EU 14 89106405 89106405 single base substitution G C intron_variant BRCA-EU 14 89107875 89107875 single base substitution C T intron_variant BRCA-EU 14 89109474 89109474 single base substitution G T intron_variant BRCA-EU 14 89114090 89114090 single base substitution G C intron_variant BRCA-EU 14 89114090 89114090 single base substitution G C upstream_gene_variant BRCA-EU 14 89114397 89114397 single base substitution G A intron_variant BRCA-EU 14 89114397 89114397 single base substitution G A upstream_gene_variant BRCA-EU 14 89115362 89115362 single base substitution G A intron_variant BRCA-EU 14 89115362 89115362 single base substitution G A upstream_gene_variant BRCA-EU 14 89115437 89115437 single base substitution C T intron_variant BRCA-EU 14 89115437 89115437 single base substitution C T upstream_gene_variant BRCA-EU 14 89115497 89115497 single base substitution C A intron_variant BRCA-EU 14 89115497 89115497 single base substitution C A upstream_gene_variant BRCA-EU 14 89115701 89115701 single base substitution G A intron_variant BRCA-EU 14 89115701 89115701 single base substitution G A upstream_gene_variant BRCA-EU 14 89116974 89116974 insertion of <=200bp - T intron_variant BRCA-EU 14 89118785 89118785 single base substitution C A intron_variant BRCA-EU 14 89119407 89119407 single base substitution T C intron_variant BRCA-EU 14 89121116 89121116 single base substitution C G intron_variant BRCA-EU 14 89122529 89122529 single base substitution C T intron_variant BRCA-EU 14 89125719 89125719 single base substitution T C intron_variant BRCA-EU 14 89126065 89126065 single base substitution T C intron_variant BRCA-EU 14 89126081 89126082 deletion of <=200bp CT - intron_variant BRCA-EU 14 89126693 89126693 single base substitution T C intron_variant BRCA-EU 14 89126771 89126771 single base substitution T C intron_variant BRCA-EU 14 89128858 89128858 single base substitution C G intron_variant BRCA-EU 14 89129732 89129762 deletion of <=200bp GTTAAAATATTTTTTAAAGTGTATCTGTTTA - intron_variant BRCA-EU 14 89130984 89130984 single base substitution A T intron_variant BRCA-EU 14 89131928 89131928 single base substitution T C intron_variant BRCA-EU 14 89131928 89131928 single base substitution T C upstream_gene_variant BRCA-EU 14 89132454 89132454 single base substitution T C intron_variant BRCA-EU 14 89132454 89132454 single base substitution T C upstream_gene_variant BRCA-EU 14 89132536 89132536 deletion of <=200bp A - intron_variant BRCA-EU 14 89132536 89132536 deletion of <=200bp A - upstream_gene_variant BRCA-EU 14 89132582 89132582 single base substitution T C intron_variant BRCA-EU 14 89132582 89132582 single base substitution T C upstream_gene_variant BRCA-EU 14 89132822 89132822 single base substitution A G intron_variant BRCA-EU 14 89132822 89132822 single base substitution A G upstream_gene_variant BRCA-EU 14 89132840 89132840 single base substitution G T intron_variant BRCA-EU 14 89132840 89132840 single base substitution G T upstream_gene_variant BRCA-EU 14 89132887 89132887 single base substitution T C intron_variant BRCA-EU 14 89132887 89132887 single base substitution T C upstream_gene_variant BRCA-EU 14 89133299 89133299 single base substitution G C intron_variant BRCA-EU 14 89133299 89133299 single base substitution G C upstream_gene_variant BRCA-EU 14 89133988 89133988 single base substitution A C intron_variant BRCA-EU 14 89133988 89133988 single base substitution A C upstream_gene_variant BRCA-EU 14 89140508 89140508 single base substitution G A intron_variant BRCA-EU 14 89142183 89142183 insertion of <=200bp - A intron_variant BRCA-EU 14 89143819 89143819 single base substitution T A intron_variant BRCA-EU 14 89148490 89148490 single base substitution T C intron_variant BRCA-EU 14 89148933 89148933 single base substitution G A intron_variant BRCA-EU 14 89149778 89149778 single base substitution G A intron_variant BRCA-EU 14 89150316 89150316 single base substitution G C intron_variant BRCA-EU 14 89152313 89152313 single base substitution C A intron_variant BRCA-EU 14 89152355 89152355 single base substitution C A intron_variant BRCA-EU 14 89152605 89152608 deletion of <=200bp AGAG - intron_variant BRCA-EU 14 89156290 89156290 single base substitution G C intron_variant BRCA-EU 14 89156711 89156711 single base substitution G A intron_variant BRCA-EU 14 89157227 89157227 single base substitution G A intron_variant BRCA-EU 14 89158844 89158844 single base substitution C T intron_variant BRCA-EU 14 89161004 89161004 single base substitution C T intron_variant BRCA-EU 14 89163095 89163095 single base substitution C A intron_variant BRCA-EU 14 89164170 89164170 single base substitution C A intron_variant BRCA-EU 14 89167301 89167301 deletion of <=200bp T - intron_variant BRCA-EU 14 89168058 89168058 single base substitution T G intron_variant BRCA-EU 14 89168811 89168811 single base substitution T C 3_prime_UTR_variant BRCA-EU 14 89168811 89168811 single base substitution T C synonymous_variant K739K 2217A>G BRCA-EU 14 89169808 89169808 single base substitution A G intron_variant BRCA-EU 14 89170175 89170175 single base substitution C T intron_variant BRCA-EU 14 89170863 89170863 single base substitution G A intron_variant BRCA-EU 14 89171608 89171608 single base substitution T C intron_variant BRCA-EU 14 89173609 89173609 single base substitution A T intron_variant BRCA-EU 14 89173930 89173930 single base substitution A G intron_variant BRCA-EU 14 89174817 89174817 single base substitution C G intron_variant BRCA-EU 14 89176499 89176499 single base substitution T C intron_variant BRCA-EU 14 89178094 89178094 single base substitution G A intron_variant BRCA-EU 14 89179449 89179449 single base substitution G A intron_variant BRCA-EU 14 89181361 89181361 single base substitution G C exon_variant BRCA-EU 14 89181361 89181361 single base substitution G C missense_variant H456D 1366C>G BRCA-EU 14 89181414 89181414 single base substitution G A exon_variant BRCA-EU 14 89181414 89181414 single base substitution G A missense_variant A438V 1313C>T BRCA-EU 14 89184599 89184599 single base substitution A C intron_variant BRCA-EU 14 89184599 89184599 single base substitution A C upstream_gene_variant BRCA-EU 14 89185566 89185566 insertion of <=200bp - A intron_variant BRCA-EU 14 89185566 89185566 insertion of <=200bp - A upstream_gene_variant BRCA-EU 14 89186297 89186297 single base substitution G A intron_variant BRCA-EU 14 89186297 89186297 single base substitution G A upstream_gene_variant BRCA-EU 14 89189007 89189007 single base substitution G A intron_variant BRCA-EU 14 89189199 89189199 single base substitution A C intron_variant BRCA-EU 14 89191990 89191990 single base substitution T C intron_variant BRCA-EU 14 89192657 89192657 single base substitution C G intron_variant BRCA-EU 14 89193104 89193107 deletion of <=200bp TTAA - intron_variant BRCA-EU 14 89195178 89195178 single base substitution A C intron_variant BRCA-EU 14 89195585 89195585 single base substitution G C intron_variant BRCA-EU 14 89195908 89195909 deletion of <=200bp TG - intron_variant BRCA-EU 14 89201250 89201250 single base substitution C T intron_variant BRCA-EU 14 89203914 89203914 single base substitution C A intron_variant BRCA-EU 14 89204257 89204257 single base substitution T C intron_variant BRCA-EU 14 89204782 89204782 single base substitution T C intron_variant BRCA-EU 14 89204996 89204996 single base substitution G C intron_variant BRCA-EU 14 89205694 89205694 single base substitution T C intron_variant BRCA-EU 14 89206289 89206289 single base substitution C A intron_variant BRCA-EU 14 89206290 89206290 single base substitution C A intron_variant BRCA-EU 14 89207144 89207144 single base substitution G C intron_variant BRCA-EU 14 89207299 89207299 single base substitution G C intron_variant BRCA-EU 14 89207740 89207740 single base substitution A C intron_variant BRCA-EU 14 89208599 89208600 deletion of <=200bp AC - intron_variant BRCA-EU 14 89208611 89208611 single base substitution A G intron_variant BRCA-EU 14 89209303 89209303 single base substitution G C intron_variant BRCA-EU 14 89209489 89209489 single base substitution G C intron_variant BRCA-EU 14 89210007 89210007 single base substitution C G intron_variant BRCA-EU 14 89211261 89211261 single base substitution C T intron_variant BRCA-EU 14 89212323 89212323 single base substitution C G intron_variant BRCA-EU 14 89214025 89214025 single base substitution G T intron_variant BRCA-EU 14 89216252 89216252 single base substitution G A intron_variant BRCA-EU 14 89216558 89216558 single base substitution C G intron_variant BRCA-EU 14 89216807 89216807 single base substitution G A intron_variant BRCA-EU 14 89217619 89217619 single base substitution G T intron_variant BRCA-EU 14 89218741 89218743 deletion of <=200bp TAT - intron_variant BRCA-EU 14 89220686 89220686 single base substitution G A intron_variant BRCA-EU 14 89220996 89220996 single base substitution G C missense_variant R73G 217C>G BRCA-EU 14 89221825 89221825 deletion of <=200bp A - intron_variant BRCA-EU 14 89222183 89222183 single base substitution A T intron_variant BRCA-EU 14 89222184 89222184 deletion of <=200bp T - intron_variant BRCA-EU 14 89222430 89222430 single base substitution G A intron_variant BRCA-EU 14 89223334 89223334 single base substitution G C intron_variant BRCA-EU 14 89223946 89223946 single base substitution G C intron_variant BRCA-EU 14 89224899 89224899 single base substitution A T intron_variant BRCA-EU 14 89226263 89226263 single base substitution T C intron_variant BRCA-EU 14 89229196 89229196 single base substitution G C intron_variant BRCA-EU 14 89229483 89229483 single base substitution G T intron_variant BRCA-EU 14 89229779 89229779 insertion of <=200bp - C intron_variant BRCA-EU 14 89230705 89230705 single base substitution G C intron_variant BRCA-EU 14 89233636 89233636 single base substitution G C intron_variant BRCA-EU 14 89234755 89234756 deletion of <=200bp GA - intron_variant BRCA-EU 14 89235176 89235176 single base substitution A C intron_variant BRCA-EU 14 89235666 89235666 single base substitution C G intron_variant BRCA-EU 14 89235767 89235767 single base substitution C A intron_variant BRCA-EU 14 89240174 89240174 single base substitution T G intron_variant BRCA-EU 14 89241036 89241036 single base substitution C A intron_variant BRCA-EU 14 89243131 89243131 single base substitution G A intron_variant BRCA-EU 14 89244139 89244139 single base substitution G A intron_variant BRCA-EU 14 89246300 89246300 single base substitution A T intron_variant BRCA-EU 14 89246301 89246301 single base substitution T A intron_variant BRCA-EU 14 89247284 89247284 single base substitution T C intron_variant BRCA-EU 14 89247830 89247830 single base substitution A G intron_variant BRCA-EU 14 89248988 89248988 single base substitution G C intron_variant BRCA-EU 14 89249058 89249058 single base substitution T C intron_variant BRCA-EU 14 89249976 89249976 single base substitution C T intron_variant BRCA-EU 14 89250391 89250391 single base substitution G C intron_variant BRCA-EU 14 89251199 89251199 single base substitution G C intron_variant BRCA-EU 14 89251778 89251778 single base substitution C G intron_variant BRCA-EU 14 89253346 89253346 single base substitution G A intron_variant BRCA-EU 14 89254142 89254142 single base substitution A G intron_variant BRCA-EU 14 89256843 89256843 single base substitution G C intron_variant BRCA-EU 14 89257423 89257423 single base substitution A G intron_variant BRCA-EU 14 89257763 89257763 single base substitution G C intron_variant BRCA-EU 14 89258072 89258072 single base substitution G T intron_variant BRCA-EU 14 89258686 89258686 single base substitution C A missense_variant Q54H 162G>T BRCA-EU 14 89261073 89261073 single base substitution G A upstream_gene_variant BRCA-EU 14 89261419 89261422 multiple base substitution (>=2bp and <=200bp) ACAT AAG upstream_gene_variant BRCA-EU 14 89261422 89261422 single base substitution T G upstream_gene_variant BRCA-EU 14 89261525 89261525 single base substitution A G upstream_gene_variant BRCA-EU 14 89263874 89263874 single base substitution G C upstream_gene_variant BRCA-FR 14 89089612 89089612 single base substitution C T downstream_gene_variant BRCA-FR 14 89089612 89089612 single base substitution C T intron_variant BRCA-FR 14 89089612 89089612 single base substitution C T upstream_gene_variant BRCA-FR 14 89089718 89089718 single base substitution G A downstream_gene_variant BRCA-FR 14 89089718 89089718 single base substitution G A intron_variant BRCA-FR 14 89089718 89089718 single base substitution G A upstream_gene_variant BRCA-FR 14 89100138 89100138 single base substitution G C intron_variant BRCA-FR 14 89100681 89100681 single base substitution C T intron_variant BRCA-FR 14 89101351 89101351 single base substitution G A intron_variant BRCA-FR 14 89106405 89106405 single base substitution G C intron_variant BRCA-FR 14 89107875 89107875 single base substitution C T intron_variant BRCA-FR 14 89113177 89113177 single base substitution A C intron_variant BRCA-FR 14 89113177 89113177 single base substitution A C upstream_gene_variant BRCA-FR 14 89116663 89116663 single base substitution T C intron_variant BRCA-FR 14 89119407 89119407 single base substitution T C intron_variant BRCA-FR 14 89143819 89143819 single base substitution T A intron_variant BRCA-FR 14 89148933 89148933 single base substitution G A intron_variant BRCA-FR 14 89151129 89151129 single base substitution A T intron_variant BRCA-FR 14 89162928 89162928 single base substitution G A intron_variant BRCA-FR 14 89168429 89168429 single base substitution G A intron_variant BRCA-FR 14 89171401 89171401 single base substitution C T intron_variant BRCA-FR 14 89183147 89183147 single base substitution G T intron_variant BRCA-FR 14 89183147 89183147 single base substitution G T upstream_gene_variant BRCA-FR 14 89193942 89193942 single base substitution A G intron_variant BRCA-FR 14 89201348 89201348 single base substitution T C intron_variant BRCA-FR 14 89217619 89217619 single base substitution G T intron_variant BRCA-FR 14 89220686 89220686 single base substitution G A intron_variant BRCA-FR 14 89229483 89229483 single base substitution G T intron_variant BRCA-FR 14 89230705 89230705 single base substitution G C intron_variant BRCA-FR 14 89247830 89247830 single base substitution A G intron_variant BRCA-FR 14 89251778 89251778 single base substitution C G intron_variant BRCA-FR 14 89253871 89253871 single base substitution T A intron_variant BRCA-FR 14 89254165 89254165 single base substitution T C intron_variant BRCA-KR 14 89168956 89168956 single base substitution C T 3_prime_UTR_variant BRCA-KR 14 89168956 89168956 single base substitution C T missense_variant R691Q 2072G>A BRCA-UK 14 89079317 89079317 single base substitution A T 3_prime_UTR_variant BRCA-UK 14 89079317 89079317 single base substitution A T downstream_gene_variant BRCA-UK 14 89080512 89080512 single base substitution G C 3_prime_UTR_variant BRCA-UK 14 89080512 89080512 single base substitution G C downstream_gene_variant BRCA-UK 14 89080512 89080512 single base substitution G C exon_variant BRCA-UK 14 89089847 89089847 single base substitution C T downstream_gene_variant BRCA-UK 14 89089847 89089847 single base substitution C T intron_variant BRCA-UK 14 89089847 89089847 single base substitution C T upstream_gene_variant BRCA-UK 14 89108086 89108086 single base substitution G A intron_variant BRCA-UK 14 89137289 89137289 single base substitution G A intron_variant BRCA-UK 14 89152355 89152355 single base substitution C A intron_variant BRCA-UK 14 89161004 89161004 single base substitution C T intron_variant BRCA-UK 14 89174817 89174817 single base substitution C G intron_variant BRCA-UK 14 89195399 89195399 single base substitution C T intron_variant BRCA-UK 14 89206290 89206290 single base substitution C A intron_variant BRCA-UK 14 89210431 89210431 single base substitution A C missense_variant F154C 461T>G BRCA-UK 14 89261910 89261910 single base substitution G A upstream_gene_variant BRCA-US 14 89077251 89077251 single base substitution G A downstream_gene_variant BRCA-US 14 89085011 89085011 single base substitution C G 3_prime_UTR_variant BRCA-US 14 89085011 89085011 single base substitution C G downstream_gene_variant BRCA-US 14 89085011 89085011 single base substitution C G exon_variant BRCA-US 14 89085011 89085011 single base substitution C G missense_variant D1795H 5383G>C BRCA-US 14 89085011 89085011 single base substitution C G missense_variant D1833H 5497G>C BRCA-US 14 89085011 89085011 single base substitution C G missense_variant D1841H 5521G>C BRCA-US 14 89085011 89085011 single base substitution C G missense_variant D251H 751G>C BRCA-US 14 89091348 89091348 single base substitution C T 3_prime_UTR_variant BRCA-US 14 89091348 89091348 single base substitution C T downstream_gene_variant BRCA-US 14 89091348 89091348 single base substitution C T exon_variant BRCA-US 14 89091348 89091348 single base substitution C T missense_variant D1576N 4726G>A BRCA-US 14 89091348 89091348 single base substitution C T missense_variant D1614N 4840G>A BRCA-US 14 89091348 89091348 single base substitution C T missense_variant D1622N 4864G>A BRCA-US 14 89091348 89091348 single base substitution C T missense_variant D63N 187G>A BRCA-US 14 89091378 89091378 single base substitution G A 3_prime_UTR_variant BRCA-US 14 89091378 89091378 single base substitution G A downstream_gene_variant BRCA-US 14 89091378 89091378 single base substitution G A exon_variant BRCA-US 14 89091378 89091378 single base substitution G A missense_variant P1566S 4696C>T BRCA-US 14 89091378 89091378 single base substitution G A missense_variant P1604S 4810C>T BRCA-US 14 89091378 89091378 single base substitution G A missense_variant P1612S 4834C>T BRCA-US 14 89091378 89091378 single base substitution G A missense_variant P53S 157C>T BRCA-US 14 89094085 89094085 deletion of <=200bp C - 3_prime_UTR_variant BRCA-US 14 89094085 89094085 deletion of <=200bp C - downstream_gene_variant BRCA-US 14 89094085 89094085 deletion of <=200bp C - frameshift_variant G1433 BRCA-US 14 89094085 89094085 deletion of <=200bp C - frameshift_variant G1471 BRCA-US 14 89094085 89094085 deletion of <=200bp C - frameshift_variant G1479 BRCA-US 14 89094085 89094085 deletion of <=200bp C - upstream_gene_variant BRCA-US 14 89105192 89105192 single base substitution G A 3_prime_UTR_variant BRCA-US 14 89105192 89105192 single base substitution G A exon_variant BRCA-US 14 89105192 89105192 single base substitution G A missense_variant H1387Y 4159C>T BRCA-US 14 89105192 89105192 single base substitution G A missense_variant H1425Y 4273C>T BRCA-US 14 89105192 89105192 single base substitution G A missense_variant H1433Y 4297C>T BRCA-US 14 89124579 89124579 deletion of <=200bp T - 3_prime_UTR_variant BRCA-US 14 89124579 89124579 deletion of <=200bp T - frameshift_variant R1239 BRCA-US 14 89124579 89124579 deletion of <=200bp T - frameshift_variant R1277 BRCA-US 14 89153606 89153606 single base substitution G T 3_prime_UTR_variant BRCA-US 14 89153606 89153606 single base substitution G T synonymous_variant L898L 2694C>A BRCA-US 14 89153606 89153606 single base substitution G T synonymous_variant L936L 2808C>A BRCA-US 14 89154694 89154694 single base substitution C T 3_prime_UTR_variant BRCA-US 14 89154694 89154694 single base substitution C T missense_variant C850Y 2549G>A BRCA-US 14 89154694 89154694 single base substitution C T missense_variant C888Y 2663G>A BRCA-US 14 89163200 89163200 single base substitution C T 3_prime_UTR_variant BRCA-US 14 89163200 89163200 single base substitution C T missense_variant D779N 2335G>A BRCA-US 14 89172755 89172755 single base substitution T A exon_variant BRCA-US 14 89172755 89172755 single base substitution T A missense_variant K558I 1673A>T BRCA-US 14 89178714 89178714 single base substitution C T exon_variant BRCA-US 14 89178714 89178714 single base substitution C T missense_variant D520N 1558G>A BRCA-US 14 89202900 89202900 single base substitution A G missense_variant V286A 857T>C BRCA-US 14 89205341 89205341 single base substitution C T missense_variant M243I 729G>A BRCA-US 14 89210436 89210436 single base substitution C T splice_acceptor_variant BRCA-US 14 89212617 89212617 single base substitution G T stop_gained S123* 368C>A BTCA-JP 14 89075593 89075593 insertion of <=200bp - T downstream_gene_variant BTCA-JP 14 89078191 89078191 single base substitution G T downstream_gene_variant BTCA-JP 14 89085071 89085071 single base substitution T G 3_prime_UTR_variant BTCA-JP 14 89085071 89085071 single base substitution T G downstream_gene_variant BTCA-JP 14 89085071 89085071 single base substitution T G exon_variant BTCA-JP 14 89085071 89085071 single base substitution T G intron_variant BTCA-JP 14 89085071 89085071 single base substitution T G missense_variant N1775H 5323A>C BTCA-JP 14 89085071 89085071 single base substitution T G missense_variant N1813H 5437A>C BTCA-JP 14 89085071 89085071 single base substitution T G missense_variant N1821H 5461A>C BTCA-JP 14 89093254 89093256 deletion of <=200bp AAG - 3_prime_UTR_variant BTCA-JP 14 89093254 89093256 deletion of <=200bp AAG - downstream_gene_variant BTCA-JP 14 89093254 89093256 deletion of <=200bp AAG - exon_variant BTCA-JP 14 89093254 89093256 deletion of <=200bp AAG - inframe_deletion L1510 BTCA-JP 14 89093254 89093256 deletion of <=200bp AAG - inframe_deletion L1548 BTCA-JP 14 89093254 89093256 deletion of <=200bp AAG - inframe_deletion L1556 BTCA-JP 14 89093254 89093256 deletion of <=200bp AAG - upstream_gene_variant BTCA-JP 14 89093307 89093307 single base substitution A C 3_prime_UTR_variant BTCA-JP 14 89093307 89093307 single base substitution A C downstream_gene_variant BTCA-JP 14 89093307 89093307 single base substitution A C missense_variant S1493A 4477T>G BTCA-JP 14 89093307 89093307 single base substitution A C missense_variant S1531A 4591T>G BTCA-JP 14 89093307 89093307 single base substitution A C missense_variant S1539A 4615T>G BTCA-JP 14 89093307 89093307 single base substitution A C upstream_gene_variant BTCA-JP 14 89105205 89105205 single base substitution G A 3_prime_UTR_variant BTCA-JP 14 89105205 89105205 single base substitution G A exon_variant BTCA-JP 14 89105205 89105205 single base substitution G A synonymous_variant L1382L 4146C>T BTCA-JP 14 89105205 89105205 single base substitution G A synonymous_variant L1420L 4260C>T BTCA-JP 14 89105205 89105205 single base substitution G A synonymous_variant L1428L 4284C>T BTCA-JP 14 89128152 89128152 single base substitution G A 3_prime_UTR_variant BTCA-JP 14 89128152 89128152 single base substitution G A missense_variant S1136L 3407C>T BTCA-JP 14 89128152 89128152 single base substitution G A missense_variant S1174L 3521C>T BTCA-JP 14 89129331 89129331 single base substitution T C intron_variant BTCA-JP 14 89153678 89153678 deletion of <=200bp A - splice_region_variant BTCA-JP 14 89171884 89171884 single base substitution T A 3_prime_UTR_variant BTCA-JP 14 89171884 89171884 single base substitution T A missense_variant D625V 1874A>T BTCA-JP 14 89212632 89212632 single base substitution T C splice_region_variant CESC-US 14 89075708 89075708 single base substitution C T downstream_gene_variant CESC-US 14 89083219 89083219 single base substitution G T 3_prime_UTR_variant CESC-US 14 89083219 89083219 single base substitution G T downstream_gene_variant CESC-US 14 89083219 89083219 single base substitution G T exon_variant CESC-US 14 89083219 89083219 single base substitution G T missense_variant L1837I 5509C>A CESC-US 14 89083219 89083219 single base substitution G T missense_variant L1875I 5623C>A CESC-US 14 89083219 89083219 single base substitution G T missense_variant L1883I 5647C>A CESC-US 14 89130940 89130940 single base substitution G T 3_prime_UTR_variant CESC-US 14 89130940 89130940 single base substitution G T exon_variant CESC-US 14 89130940 89130940 single base substitution G T synonymous_variant S1064S 3192C>A CESC-US 14 89130940 89130940 single base substitution G T synonymous_variant S1102S 3306C>A CESC-US 14 89181361 89181361 single base substitution G A exon_variant CESC-US 14 89181361 89181361 single base substitution G A missense_variant H456Y 1366C>T CLLE-ES 14 89076848 89076848 single base substitution C T downstream_gene_variant CLLE-ES 14 89132346 89132346 single base substitution T C intron_variant CLLE-ES 14 89132346 89132346 single base substitution T C upstream_gene_variant CLLE-ES 14 89138180 89138180 single base substitution C T intron_variant CLLE-ES 14 89251364 89251364 single base substitution C T intron_variant CLLE-ES 14 89256701 89256701 single base substitution A G intron_variant COAD-US 14 89082558 89082558 single base substitution G A 3_prime_UTR_variant COAD-US 14 89082558 89082558 single base substitution G A downstream_gene_variant COAD-US 14 89082558 89082558 single base substitution G A exon_variant COAD-US 14 89082558 89082558 single base substitution G A missense_variant S1896L 5687C>T COAD-US 14 89082558 89082558 single base substitution G A missense_variant S1934L 5801C>T COAD-US 14 89082558 89082558 single base substitution G A missense_variant S1942L 5825C>T COAD-US 14 89085018 89085018 single base substitution G T 3_prime_UTR_variant COAD-US 14 89085018 89085018 single base substitution G T downstream_gene_variant COAD-US 14 89085018 89085018 single base substitution G T exon_variant COAD-US 14 89085018 89085018 single base substitution G T missense_variant F1792L 5376C>A COAD-US 14 89085018 89085018 single base substitution G T missense_variant F1830L 5490C>A COAD-US 14 89085018 89085018 single base substitution G T missense_variant F1838L 5514C>A COAD-US 14 89085018 89085018 single base substitution G T missense_variant F248L 744C>A COAD-US 14 89087182 89087182 deletion of <=200bp T - 3_prime_UTR_variant COAD-US 14 89087182 89087182 deletion of <=200bp T - downstream_gene_variant COAD-US 14 89087182 89087182 deletion of <=200bp T - frameshift_variant N1718 COAD-US 14 89087182 89087182 deletion of <=200bp T - frameshift_variant N1756 COAD-US 14 89087182 89087182 deletion of <=200bp T - frameshift_variant N1764 COAD-US 14 89087182 89087182 deletion of <=200bp T - frameshift_variant N204 COAD-US 14 89087182 89087182 deletion of <=200bp T - upstream_gene_variant COAD-US 14 89123739 89123739 single base substitution C A 3_prime_UTR_variant COAD-US 14 89123739 89123739 single base substitution C A stop_gained E1291* 3871G>T COAD-US 14 89123739 89123739 single base substitution C A stop_gained E1329* 3985G>T COAD-US 14 89130896 89130896 single base substitution C T 3_prime_UTR_variant COAD-US 14 89130896 89130896 single base substitution C T exon_variant COAD-US 14 89130896 89130896 single base substitution C T missense_variant R1079Q 3236G>A COAD-US 14 89130896 89130896 single base substitution C T missense_variant R1117Q 3350G>A COAD-US 14 89131804 89131804 single base substitution C T 3_prime_UTR_variant COAD-US 14 89131804 89131804 single base substitution C T missense_variant G1014S 3040G>A COAD-US 14 89131804 89131804 single base substitution C T missense_variant G1052S 3154G>A COAD-US 14 89131804 89131804 single base substitution C T upstream_gene_variant COAD-US 14 89148335 89148335 single base substitution G T 3_prime_UTR_variant COAD-US 14 89148335 89148335 single base substitution G T missense_variant P1008H 3023C>A COAD-US 14 89148335 89148335 single base substitution G T missense_variant P970H 2909C>A COAD-US 14 89151392 89151392 single base substitution C A 3_prime_UTR_variant COAD-US 14 89151392 89151392 single base substitution C A synonymous_variant V945V 2835G>T COAD-US 14 89151392 89151392 single base substitution C A synonymous_variant V983V 2949G>T COAD-US 14 89172769 89172769 single base substitution C T splice_region_variant COAD-US 14 89178614 89178614 single base substitution C T splice_donor_variant COAD-US 14 89192963 89192963 single base substitution C T missense_variant R370H 1109G>A COAD-US 14 89202845 89202845 single base substitution T G missense_variant E304D 912A>C COAD-US 14 89220912 89220912 single base substitution A C missense_variant L101V 301T>G COAD-US 14 89258716 89258716 single base substitution G A synonymous_variant G44G 132C>T COCA-CN 14 89077272 89077272 single base substitution G A downstream_gene_variant COCA-CN 14 89077329 89077329 single base substitution T G downstream_gene_variant COCA-CN 14 89078018 89078018 single base substitution T A downstream_gene_variant COCA-CN 14 89082537 89082537 single base substitution C T 3_prime_UTR_variant COCA-CN 14 89082537 89082537 single base substitution C T downstream_gene_variant COCA-CN 14 89082537 89082537 single base substitution C T exon_variant COCA-CN 14 89082537 89082537 single base substitution C T missense_variant R1903Q 5708G>A COCA-CN 14 89082537 89082537 single base substitution C T missense_variant R1941Q 5822G>A COCA-CN 14 89082537 89082537 single base substitution C T missense_variant R1949Q 5846G>A COCA-CN 14 89084926 89084926 single base substitution G A downstream_gene_variant COCA-CN 14 89084926 89084926 single base substitution G A intron_variant COCA-CN 14 89091337 89091337 single base substitution G A 3_prime_UTR_variant COCA-CN 14 89091337 89091337 single base substitution G A downstream_gene_variant COCA-CN 14 89091337 89091337 single base substitution G A exon_variant COCA-CN 14 89091337 89091337 single base substitution G A synonymous_variant I1579I 4737C>T COCA-CN 14 89091337 89091337 single base substitution G A synonymous_variant I1617I 4851C>T COCA-CN 14 89091337 89091337 single base substitution G A synonymous_variant I1625I 4875C>T COCA-CN 14 89091337 89091337 single base substitution G A synonymous_variant I66I 198C>T COCA-CN 14 89093425 89093425 single base substitution C A downstream_gene_variant COCA-CN 14 89093425 89093425 single base substitution C A intron_variant COCA-CN 14 89093425 89093425 single base substitution C A upstream_gene_variant COCA-CN 14 89093488 89093488 single base substitution G A downstream_gene_variant COCA-CN 14 89093488 89093488 single base substitution G A intron_variant COCA-CN 14 89093488 89093488 single base substitution G A upstream_gene_variant COCA-CN 14 89105287 89105287 single base substitution T A intron_variant COCA-CN 14 89110861 89110861 single base substitution A G exon_variant COCA-CN 14 89110861 89110861 single base substitution A G splice_region_variant COCA-CN 14 89116455 89116455 single base substitution G T intron_variant COCA-CN 14 89123727 89123727 single base substitution C T 3_prime_UTR_variant COCA-CN 14 89123727 89123727 single base substitution C T missense_variant D1295N 3883G>A COCA-CN 14 89123727 89123727 single base substitution C T missense_variant D1333N 3997G>A COCA-CN 14 89124527 89124527 single base substitution G A splice_region_variant COCA-CN 14 89124623 89124623 single base substitution G T 3_prime_UTR_variant COCA-CN 14 89124623 89124623 single base substitution G T missense_variant S1224Y 3671C>A COCA-CN 14 89124623 89124623 single base substitution G T missense_variant S1262Y 3785C>A COCA-CN 14 89124633 89124633 single base substitution T C 3_prime_UTR_variant COCA-CN 14 89124633 89124633 single base substitution T C missense_variant T1221A 3661A>G COCA-CN 14 89124633 89124633 single base substitution T C missense_variant T1259A 3775A>G COCA-CN 14 89124675 89124675 single base substitution G A 3_prime_UTR_variant COCA-CN 14 89124675 89124675 single base substitution G A missense_variant R1207C 3619C>T COCA-CN 14 89124675 89124675 single base substitution G A missense_variant R1245C 3733C>T COCA-CN 14 89129473 89129473 single base substitution A C intron_variant COCA-CN 14 89130930 89130930 single base substitution A C 3_prime_UTR_variant COCA-CN 14 89130930 89130930 single base substitution A C exon_variant COCA-CN 14 89130930 89130930 single base substitution A C missense_variant F1068V 3202T>G COCA-CN 14 89130930 89130930 single base substitution A C missense_variant F1106V 3316T>G COCA-CN 14 89148231 89148231 single base substitution T C splice_region_variant COCA-CN 14 89154835 89154835 single base substitution T G intron_variant COCA-CN 14 89154939 89154939 single base substitution G A intron_variant COCA-CN 14 89160731 89160731 single base substitution A C 3_prime_UTR_variant COCA-CN 14 89160731 89160731 single base substitution A C missense_variant F820C 2459T>G COCA-CN 14 89161627 89161627 single base substitution A T intron_variant COCA-CN 14 89161722 89161722 single base substitution C A 3_prime_UTR_variant COCA-CN 14 89161722 89161722 single base substitution C A missense_variant E807D 2421G>T COCA-CN 14 89163267 89163267 single base substitution C T 3_prime_UTR_variant COCA-CN 14 89163267 89163267 single base substitution C T stop_gained W756* 2268G>A COCA-CN 14 89172755 89172755 single base substitution T G exon_variant COCA-CN 14 89172755 89172755 single base substitution T G missense_variant K558T 1673A>C COCA-CN 14 89181550 89181550 single base substitution G T intron_variant COCA-CN 14 89181550 89181550 single base substitution G T upstream_gene_variant COCA-CN 14 89182105 89182105 single base substitution G A intron_variant COCA-CN 14 89182105 89182105 single base substitution G A upstream_gene_variant COCA-CN 14 89205292 89205292 single base substitution G A missense_variant R260C 778C>T COCA-CN 14 89205352 89205352 single base substitution T G missense_variant I240L 718A>C COCA-CN 14 89220990 89220990 single base substitution A C missense_variant L75V 223T>G COCA-CN 14 89222184 89222184 single base substitution T A intron_variant COCA-CN 14 89262447 89262447 single base substitution G A upstream_gene_variant EOPC-DE 14 89074673 89074673 single base substitution T C downstream_gene_variant EOPC-DE 14 89106969 89106969 single base substitution C G intron_variant EOPC-DE 14 89128630 89128630 single base substitution T A intron_variant ESAD-UK 14 89075494 89075494 insertion of <=200bp - T downstream_gene_variant ESAD-UK 14 89078478 89078478 single base substitution G T downstream_gene_variant ESAD-UK 14 89079131 89079131 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 14 89079131 89079131 deletion of <=200bp T - downstream_gene_variant ESAD-UK 14 89081878 89081878 single base substitution C T 3_prime_UTR_variant ESAD-UK 14 89081878 89081878 single base substitution C T downstream_gene_variant ESAD-UK 14 89081878 89081878 single base substitution C T exon_variant ESAD-UK 14 89081974 89081974 single base substitution C T 3_prime_UTR_variant ESAD-UK 14 89081974 89081974 single base substitution C T downstream_gene_variant ESAD-UK 14 89081974 89081974 single base substitution C T exon_variant ESAD-UK 14 89089132 89089132 single base substitution C G downstream_gene_variant ESAD-UK 14 89089132 89089132 single base substitution C G intron_variant ESAD-UK 14 89089132 89089132 single base substitution C G upstream_gene_variant ESAD-UK 14 89089160 89089160 insertion of <=200bp - A downstream_gene_variant ESAD-UK 14 89089160 89089160 insertion of <=200bp - A intron_variant ESAD-UK 14 89089160 89089160 insertion of <=200bp - A upstream_gene_variant ESAD-UK 14 89090761 89090761 single base substitution A T downstream_gene_variant ESAD-UK 14 89090761 89090761 single base substitution A T intron_variant ESAD-UK 14 89090761 89090761 single base substitution A T upstream_gene_variant ESAD-UK 14 89092785 89092785 single base substitution G A downstream_gene_variant ESAD-UK 14 89092785 89092785 single base substitution G A intron_variant ESAD-UK 14 89097007 89097007 single base substitution C T intron_variant ESAD-UK 14 89097007 89097007 single base substitution C T upstream_gene_variant ESAD-UK 14 89098939 89098939 single base substitution A C intron_variant ESAD-UK 14 89099175 89099175 single base substitution A C intron_variant ESAD-UK 14 89099325 89099325 single base substitution C T intron_variant ESAD-UK 14 89102144 89102144 single base substitution G A intron_variant ESAD-UK 14 89102457 89102457 single base substitution A C intron_variant ESAD-UK 14 89102458 89102458 single base substitution G A intron_variant ESAD-UK 14 89102777 89102777 single base substitution C T intron_variant ESAD-UK 14 89103001 89103001 single base substitution T A intron_variant ESAD-UK 14 89103827 89103827 single base substitution A T intron_variant ESAD-UK 14 89104129 89104129 single base substitution T A intron_variant ESAD-UK 14 89105602 89105602 insertion of <=200bp - G intron_variant ESAD-UK 14 89105906 89105906 single base substitution G T intron_variant ESAD-UK 14 89106762 89106762 single base substitution C T intron_variant ESAD-UK 14 89106980 89106980 single base substitution C G intron_variant ESAD-UK 14 89107332 89107334 deletion of <=200bp AAG - intron_variant ESAD-UK 14 89107601 89107601 single base substitution C T intron_variant ESAD-UK 14 89108336 89108336 single base substitution A C intron_variant ESAD-UK 14 89111107 89111107 single base substitution T A intron_variant ESAD-UK 14 89111107 89111107 single base substitution T A upstream_gene_variant ESAD-UK 14 89113344 89113344 single base substitution T G intron_variant ESAD-UK 14 89113344 89113344 single base substitution T G upstream_gene_variant ESAD-UK 14 89115662 89115662 single base substitution G A intron_variant ESAD-UK 14 89115662 89115662 single base substitution G A upstream_gene_variant ESAD-UK 14 89116973 89116973 single base substitution A T intron_variant ESAD-UK 14 89117811 89117811 single base substitution A C intron_variant ESAD-UK 14 89118002 89118002 single base substitution C T intron_variant ESAD-UK 14 89121225 89121225 single base substitution A C intron_variant ESAD-UK 14 89121448 89121448 single base substitution C G intron_variant ESAD-UK 14 89121565 89121565 single base substitution C T intron_variant ESAD-UK 14 89121661 89121661 single base substitution A G intron_variant ESAD-UK 14 89123223 89123223 single base substitution C T intron_variant ESAD-UK 14 89124121 89124121 single base substitution G C intron_variant ESAD-UK 14 89124302 89124302 single base substitution T C intron_variant ESAD-UK 14 89124490 89124490 single base substitution T G intron_variant ESAD-UK 14 89124527 89124527 single base substitution G A splice_region_variant ESAD-UK 14 89126465 89126465 insertion of <=200bp - T intron_variant ESAD-UK 14 89126465 89126465 single base substitution A T intron_variant ESAD-UK 14 89130377 89130377 single base substitution T G intron_variant ESAD-UK 14 89132580 89132580 insertion of <=200bp - T intron_variant ESAD-UK 14 89132580 89132580 insertion of <=200bp - T upstream_gene_variant ESAD-UK 14 89132801 89132801 single base substitution C A intron_variant ESAD-UK 14 89132801 89132801 single base substitution C A upstream_gene_variant ESAD-UK 14 89132836 89132836 single base substitution C T intron_variant ESAD-UK 14 89132836 89132836 single base substitution C T upstream_gene_variant ESAD-UK 14 89133067 89133067 single base substitution A T intron_variant ESAD-UK 14 89133067 89133067 single base substitution A T upstream_gene_variant ESAD-UK 14 89133382 89133382 single base substitution T A intron_variant ESAD-UK 14 89133382 89133382 single base substitution T A upstream_gene_variant ESAD-UK 14 89133971 89133971 single base substitution A G intron_variant ESAD-UK 14 89133971 89133971 single base substitution A G upstream_gene_variant ESAD-UK 14 89134252 89134252 single base substitution G A intron_variant ESAD-UK 14 89134252 89134252 single base substitution G A upstream_gene_variant ESAD-UK 14 89134659 89134659 single base substitution A G intron_variant ESAD-UK 14 89134659 89134659 single base substitution A G upstream_gene_variant ESAD-UK 14 89135142 89135142 single base substitution T A intron_variant ESAD-UK 14 89135142 89135142 single base substitution T A upstream_gene_variant ESAD-UK 14 89136050 89136050 single base substitution C A intron_variant ESAD-UK 14 89136050 89136050 single base substitution C A upstream_gene_variant ESAD-UK 14 89136725 89136725 single base substitution A T intron_variant ESAD-UK 14 89137572 89137572 single base substitution A G intron_variant ESAD-UK 14 89138926 89138926 single base substitution C T intron_variant ESAD-UK 14 89139403 89139403 single base substitution C A intron_variant ESAD-UK 14 89141993 89141993 single base substitution C G intron_variant ESAD-UK 14 89142860 89142860 single base substitution A T intron_variant ESAD-UK 14 89144526 89144526 single base substitution A T intron_variant ESAD-UK 14 89148766 89148766 single base substitution G A intron_variant ESAD-UK 14 89151013 89151013 single base substitution T C intron_variant ESAD-UK 14 89151298 89151299 deletion of <=200bp TA - intron_variant ESAD-UK 14 89151349 89151349 single base substitution T A intron_variant ESAD-UK 14 89151905 89151905 single base substitution A T intron_variant ESAD-UK 14 89152711 89152711 single base substitution C T intron_variant ESAD-UK 14 89154109 89154109 single base substitution C A intron_variant ESAD-UK 14 89154110 89154110 single base substitution A C intron_variant ESAD-UK 14 89155074 89155074 insertion of <=200bp - T intron_variant ESAD-UK 14 89159816 89159816 single base substitution C T intron_variant ESAD-UK 14 89162483 89162483 single base substitution T A intron_variant ESAD-UK 14 89162882 89162882 single base substitution C T intron_variant ESAD-UK 14 89164854 89164854 single base substitution C T intron_variant ESAD-UK 14 89165638 89165638 deletion of <=200bp A - intron_variant ESAD-UK 14 89165923 89165923 single base substitution G C intron_variant ESAD-UK 14 89166291 89166291 single base substitution T C intron_variant ESAD-UK 14 89166939 89166939 single base substitution T C intron_variant ESAD-UK 14 89167301 89167301 single base substitution T G intron_variant ESAD-UK 14 89169934 89169934 single base substitution G C intron_variant ESAD-UK 14 89170003 89170003 single base substitution C T intron_variant ESAD-UK 14 89170149 89170149 single base substitution T C intron_variant ESAD-UK 14 89170317 89170317 single base substitution C T intron_variant ESAD-UK 14 89171736 89171736 single base substitution C A intron_variant ESAD-UK 14 89173125 89173125 single base substitution A G intron_variant ESAD-UK 14 89174531 89174531 single base substitution A T intron_variant ESAD-UK 14 89174659 89174659 single base substitution A T intron_variant ESAD-UK 14 89176179 89176179 insertion of <=200bp - A intron_variant ESAD-UK 14 89176297 89176297 single base substitution G A intron_variant ESAD-UK 14 89177129 89177129 single base substitution T G intron_variant ESAD-UK 14 89177309 89177309 single base substitution T G intron_variant ESAD-UK 14 89177690 89177690 single base substitution T G intron_variant ESAD-UK 14 89178814 89178814 single base substitution C T exon_variant ESAD-UK 14 89178814 89178814 single base substitution C T synonymous_variant V486V 1458G>A ESAD-UK 14 89179557 89179557 deletion of <=200bp A - intron_variant ESAD-UK 14 89182950 89182950 single base substitution G T intron_variant ESAD-UK 14 89182950 89182950 single base substitution G T upstream_gene_variant ESAD-UK 14 89183498 89183498 single base substitution C A intron_variant ESAD-UK 14 89183498 89183498 single base substitution C A upstream_gene_variant ESAD-UK 14 89187650 89187650 single base substitution C T intron_variant ESAD-UK 14 89187863 89187863 single base substitution G T intron_variant ESAD-UK 14 89190061 89190062 deletion of <=200bp AC - intron_variant ESAD-UK 14 89192500 89192500 insertion of <=200bp - AAC intron_variant ESAD-UK 14 89192767 89192767 single base substitution A C intron_variant ESAD-UK 14 89192969 89192969 single base substitution G A missense_variant P368L 1103C>T ESAD-UK 14 89193961 89193961 single base substitution C T intron_variant ESAD-UK 14 89194032 89194032 single base substitution G A intron_variant ESAD-UK 14 89194285 89194285 single base substitution T C intron_variant ESAD-UK 14 89194783 89194784 deletion of <=200bp AC - intron_variant ESAD-UK 14 89195006 89195006 single base substitution G A intron_variant ESAD-UK 14 89196215 89196215 single base substitution T G intron_variant ESAD-UK 14 89199901 89199901 single base substitution T G intron_variant ESAD-UK 14 89200567 89200567 single base substitution T G intron_variant ESAD-UK 14 89201857 89201857 single base substitution T G intron_variant ESAD-UK 14 89203213 89203213 single base substitution T A intron_variant ESAD-UK 14 89205759 89205759 insertion of <=200bp - C intron_variant ESAD-UK 14 89206757 89206757 single base substitution T C missense_variant I229V 685A>G ESAD-UK 14 89207520 89207520 single base substitution T A intron_variant ESAD-UK 14 89207755 89207755 single base substitution T A intron_variant ESAD-UK 14 89208980 89208980 single base substitution G A intron_variant ESAD-UK 14 89210886 89210886 single base substitution T C intron_variant ESAD-UK 14 89211973 89211973 single base substitution C G intron_variant ESAD-UK 14 89212473 89212473 single base substitution C T intron_variant ESAD-UK 14 89213157 89213157 single base substitution G A intron_variant ESAD-UK 14 89213392 89213392 single base substitution C T intron_variant ESAD-UK 14 89213850 89213850 single base substitution A C intron_variant ESAD-UK 14 89213949 89213949 single base substitution G A intron_variant ESAD-UK 14 89214108 89214108 single base substitution G A intron_variant ESAD-UK 14 89215083 89215083 insertion of <=200bp - A intron_variant ESAD-UK 14 89217208 89217208 single base substitution G A intron_variant ESAD-UK 14 89217226 89217226 single base substitution A G intron_variant ESAD-UK 14 89217504 89217504 single base substitution C T intron_variant ESAD-UK 14 89219369 89219369 single base substitution C A intron_variant ESAD-UK 14 89220695 89220695 single base substitution A C intron_variant ESAD-UK 14 89221725 89221725 single base substitution T G intron_variant ESAD-UK 14 89221754 89221754 single base substitution C A intron_variant ESAD-UK 14 89222184 89222184 deletion of <=200bp T - intron_variant ESAD-UK 14 89222184 89222184 single base substitution T A intron_variant ESAD-UK 14 89222348 89222348 single base substitution A T intron_variant ESAD-UK 14 89224518 89224518 insertion of <=200bp - AT intron_variant ESAD-UK 14 89227277 89227277 single base substitution T G intron_variant ESAD-UK 14 89227554 89227554 single base substitution T A intron_variant ESAD-UK 14 89228152 89228152 single base substitution C T intron_variant ESAD-UK 14 89228393 89228393 single base substitution G C intron_variant ESAD-UK 14 89230317 89230317 single base substitution C A intron_variant ESAD-UK 14 89230510 89230510 single base substitution A C intron_variant ESAD-UK 14 89230841 89230841 single base substitution C A intron_variant ESAD-UK 14 89231553 89231553 single base substitution C T intron_variant ESAD-UK 14 89232465 89232465 single base substitution G A intron_variant ESAD-UK 14 89233728 89233728 single base substitution C T intron_variant ESAD-UK 14 89234218 89234218 single base substitution A G intron_variant ESAD-UK 14 89234365 89234365 insertion of <=200bp - CCTTC intron_variant ESAD-UK 14 89234379 89234379 single base substitution T G intron_variant ESAD-UK 14 89236685 89236685 insertion of <=200bp - T intron_variant ESAD-UK 14 89237704 89237705 deletion of <=200bp CT - intron_variant ESAD-UK 14 89237731 89237731 single base substitution C A intron_variant ESAD-UK 14 89239192 89239192 single base substitution A G intron_variant ESAD-UK 14 89239737 89239737 single base substitution G A intron_variant ESAD-UK 14 89239781 89239781 single base substitution C T intron_variant ESAD-UK 14 89239983 89239983 single base substitution C T intron_variant ESAD-UK 14 89241029 89241029 single base substitution A G intron_variant ESAD-UK 14 89241678 89241678 single base substitution T C intron_variant ESAD-UK 14 89244043 89244043 single base substitution G A intron_variant ESAD-UK 14 89244428 89244428 single base substitution G A intron_variant ESAD-UK 14 89246151 89246151 single base substitution G T intron_variant ESAD-UK 14 89246300 89246300 single base substitution A T intron_variant ESAD-UK 14 89247739 89247739 single base substitution G C intron_variant ESAD-UK 14 89250711 89250711 single base substitution T A intron_variant ESAD-UK 14 89253374 89253374 single base substitution G A intron_variant ESAD-UK 14 89253912 89253912 single base substitution C G intron_variant ESAD-UK 14 89256470 89256470 single base substitution T A intron_variant ESAD-UK 14 89261868 89261868 single base substitution G C upstream_gene_variant ESAD-UK 14 89263463 89263463 insertion of <=200bp - TA upstream_gene_variant ESCA-CN 14 89081729 89081729 single base substitution T C 3_prime_UTR_variant ESCA-CN 14 89081729 89081729 single base substitution T C downstream_gene_variant ESCA-CN 14 89081729 89081729 single base substitution T C exon_variant ESCA-CN 14 89171876 89171876 single base substitution C G 3_prime_UTR_variant ESCA-CN 14 89171876 89171876 single base substitution C G missense_variant E628Q 1882G>C ESCA-CN 14 89181490 89181490 single base substitution C T missense_variant E413K 1237G>A ESCA-CN 14 89181490 89181490 single base substitution C T upstream_gene_variant GBM-US 14 89084607 89084607 single base substitution G A 3_prime_UTR_variant GBM-US 14 89084607 89084607 single base substitution G A downstream_gene_variant GBM-US 14 89084607 89084607 single base substitution G A exon_variant GBM-US 14 89084607 89084607 single base substitution G A synonymous_variant A1823A 5469C>T GBM-US 14 89084607 89084607 single base substitution G A synonymous_variant A1861A 5583C>T GBM-US 14 89084607 89084607 single base substitution G A synonymous_variant A1869A 5607C>T GBM-US 14 89130847 89130847 single base substitution C T 3_prime_UTR_variant GBM-US 14 89130847 89130847 single base substitution C T exon_variant GBM-US 14 89130847 89130847 single base substitution C T stop_gained W1095* 3285G>A GBM-US 14 89130847 89130847 single base substitution C T stop_gained W1133* 3399G>A GBM-US 14 89160659 89160659 single base substitution C T 3_prime_UTR_variant GBM-US 14 89160659 89160659 single base substitution C T missense_variant R844H 2531G>A GBM-US 14 89168805 89168805 single base substitution G A 3_prime_UTR_variant GBM-US 14 89168805 89168805 single base substitution G A synonymous_variant Y741Y 2223C>T KIRC-US 14 89093186 89093186 single base substitution C T 3_prime_UTR_variant KIRC-US 14 89093186 89093186 single base substitution C T downstream_gene_variant KIRC-US 14 89093186 89093186 single base substitution C T exon_variant KIRC-US 14 89093186 89093186 single base substitution C T missense_variant G1533D 4598G>A KIRC-US 14 89093186 89093186 single base substitution C T missense_variant G1571D 4712G>A KIRC-US 14 89093186 89093186 single base substitution C T missense_variant G1579D 4736G>A KIRC-US 14 89093186 89093186 single base substitution C T missense_variant G20D 59G>A KIRC-US 14 89128141 89128141 single base substitution C A 3_prime_UTR_variant KIRC-US 14 89128141 89128141 single base substitution C A missense_variant V1140L 3418G>T KIRC-US 14 89128141 89128141 single base substitution C A missense_variant V1178L 3532G>T KIRC-US 14 89168918 89168918 single base substitution A T 3_prime_UTR_variant KIRC-US 14 89168918 89168918 single base substitution A T missense_variant Y704N 2110T>A KIRC-US 14 89168919 89168919 single base substitution C G 3_prime_UTR_variant KIRC-US 14 89168919 89168919 single base substitution C G synonymous_variant V703V 2109G>C KIRC-US 14 89202708 89202708 single base substitution C G missense_variant R350T 1049G>C KIRC-US 14 89202868 89202868 single base substitution G C missense_variant L297V 889C>G KIRP-US 14 89105224 89105224 single base substitution T G 3_prime_UTR_variant KIRP-US 14 89105224 89105224 single base substitution T G exon_variant KIRP-US 14 89105224 89105224 single base substitution T G missense_variant N1376T 4127A>C KIRP-US 14 89105224 89105224 single base substitution T G missense_variant N1414T 4241A>C KIRP-US 14 89105224 89105224 single base substitution T G missense_variant N1422T 4265A>C KIRP-US 14 89161727 89161727 single base substitution C T 3_prime_UTR_variant KIRP-US 14 89161727 89161727 single base substitution C T missense_variant G806R 2416G>A KIRP-US 14 89171882 89171882 insertion of <=200bp - T 3_prime_UTR_variant KIRP-US 14 89171882 89171882 insertion of <=200bp - T frameshift_variant V626D? LAML-KR 14 89074131 89074131 single base substitution T C downstream_gene_variant LAML-KR 14 89074206 89074206 single base substitution T C downstream_gene_variant LAML-KR 14 89074259 89074259 single base substitution C T downstream_gene_variant LAML-KR 14 89074478 89074478 single base substitution T C downstream_gene_variant LAML-KR 14 89074554 89074554 single base substitution T C downstream_gene_variant LAML-KR 14 89087565 89087565 single base substitution G A 3_prime_UTR_variant LAML-KR 14 89087565 89087565 single base substitution G A downstream_gene_variant LAML-KR 14 89087565 89087565 single base substitution G A exon_variant LAML-KR 14 89087565 89087565 single base substitution G A synonymous_variant N139N 417C>T LAML-KR 14 89087565 89087565 single base substitution G A synonymous_variant N1652N 4956C>T LAML-KR 14 89087565 89087565 single base substitution G A synonymous_variant N1690N 5070C>T LAML-KR 14 89087565 89087565 single base substitution G A synonymous_variant N1698N 5094C>T LAML-KR 14 89087565 89087565 single base substitution G A upstream_gene_variant LAML-KR 14 89205265 89205265 single base substitution T C missense_variant I269V 805A>G LAML-KR 14 89211515 89211515 single base substitution G T intron_variant LAML-KR 14 89262188 89262188 single base substitution G A upstream_gene_variant LGG-US 14 89093251 89093251 single base substitution G C 3_prime_UTR_variant LGG-US 14 89093251 89093251 single base substitution G C downstream_gene_variant LGG-US 14 89093251 89093251 single base substitution G C exon_variant LGG-US 14 89093251 89093251 single base substitution G C missense_variant S1511R 4533C>G LGG-US 14 89093251 89093251 single base substitution G C missense_variant S1549R 4647C>G LGG-US 14 89093251 89093251 single base substitution G C missense_variant S1557R 4671C>G LGG-US 14 89093251 89093251 single base substitution G C upstream_gene_variant LGG-US 14 89154773 89154773 single base substitution T C intron_variant LGG-US 14 89154773 89154773 single base substitution T C missense_variant K862E 2584A>G LGG-US 14 89160703 89160703 single base substitution A T 3_prime_UTR_variant LGG-US 14 89160703 89160703 single base substitution A T synonymous_variant P829P 2487T>A LICA-FR 14 89109501 89109501 single base substitution A G intron_variant LICA-FR 14 89119658 89119658 single base substitution C T intron_variant LICA-FR 14 89123720 89123720 single base substitution C A missense_variant R1297M 3890G>T LICA-FR 14 89123720 89123720 single base substitution C A missense_variant R1335M 4004G>T LICA-FR 14 89123720 89123720 single base substitution C A splice_region_variant LICA-FR 14 89131891 89131891 single base substitution C T intron_variant LICA-FR 14 89131891 89131891 single base substitution C T upstream_gene_variant LICA-FR 14 89132124 89132124 single base substitution C T intron_variant LICA-FR 14 89132124 89132124 single base substitution C T upstream_gene_variant LICA-FR 14 89148282 89148282 single base substitution C T 3_prime_UTR_variant LICA-FR 14 89148282 89148282 single base substitution C T missense_variant D1026N 3076G>A LICA-FR 14 89148282 89148282 single base substitution C T missense_variant D988N 2962G>A LICA-FR 14 89153736 89153736 single base substitution C T intron_variant LICA-FR 14 89164599 89164599 single base substitution C T intron_variant LICA-FR 14 89181498 89181498 single base substitution G A missense_variant A410V 1229C>T LICA-FR 14 89181498 89181498 single base substitution G A upstream_gene_variant LICA-FR 14 89184766 89184766 single base substitution G A intron_variant LICA-FR 14 89184766 89184766 single base substitution G A upstream_gene_variant LICA-FR 14 89190618 89190618 deletion of <=200bp A - intron_variant LICA-FR 14 89193016 89193016 single base substitution C A missense_variant W352C 1056G>T LICA-FR 14 89193022 89193022 single base substitution C T splice_region_variant LICA-FR 14 89220980 89220980 single base substitution G T missense_variant T78K 233C>A LICA-FR 14 89236179 89236179 single base substitution T C intron_variant LIHC-US 14 89124556 89124556 single base substitution G T 3_prime_UTR_variant LIHC-US 14 89124556 89124556 single base substitution G T synonymous_variant S1246S 3738C>A LIHC-US 14 89124556 89124556 single base substitution G T synonymous_variant S1284S 3852C>A LIHC-US 14 89154769 89154769 deletion of <=200bp T - frameshift_variant N863 LIHC-US 14 89154769 89154769 deletion of <=200bp T - intron_variant LIHC-US 14 89202777 89202777 single base substitution T A missense_variant E327V 980A>T LIHC-US 14 89206879 89206879 single base substitution C T missense_variant R188Q 563G>A LINC-JP 14 89081303 89081303 single base substitution A G 3_prime_UTR_variant LINC-JP 14 89081303 89081303 single base substitution A G downstream_gene_variant LINC-JP 14 89081303 89081303 single base substitution A G exon_variant LINC-JP 14 89084677 89084677 single base substitution T C downstream_gene_variant LINC-JP 14 89084677 89084677 single base substitution T C splice_acceptor_variant LINC-JP 14 89087296 89087296 single base substitution G A downstream_gene_variant LINC-JP 14 89087296 89087296 single base substitution G A intron_variant LINC-JP 14 89087296 89087296 single base substitution G A upstream_gene_variant LINC-JP 14 89087848 89087848 single base substitution A G downstream_gene_variant LINC-JP 14 89087848 89087848 single base substitution A G intron_variant LINC-JP 14 89087848 89087848 single base substitution A G upstream_gene_variant LINC-JP 14 89088968 89088968 single base substitution G A 3_prime_UTR_variant LINC-JP 14 89088968 89088968 single base substitution G A intron_variant LINC-JP 14 89088968 89088968 single base substitution G A missense_variant R106C 316C>T LINC-JP 14 89088968 89088968 single base substitution G A missense_variant R1619C 4855C>T LINC-JP 14 89088968 89088968 single base substitution G A missense_variant R1657C 4969C>T LINC-JP 14 89088968 89088968 single base substitution G A missense_variant R1665C 4993C>T LINC-JP 14 89088968 89088968 single base substitution G A upstream_gene_variant LINC-JP 14 89089165 89089165 single base substitution G A downstream_gene_variant LINC-JP 14 89089165 89089165 single base substitution G A intron_variant LINC-JP 14 89089165 89089165 single base substitution G A upstream_gene_variant LINC-JP 14 89093336 89093336 single base substitution A C 3_prime_UTR_variant LINC-JP 14 89093336 89093336 single base substitution A C downstream_gene_variant LINC-JP 14 89093336 89093336 single base substitution A C missense_variant F1483C 4448T>G LINC-JP 14 89093336 89093336 single base substitution A C missense_variant F1521C 4562T>G LINC-JP 14 89093336 89093336 single base substitution A C missense_variant F1529C 4586T>G LINC-JP 14 89093336 89093336 single base substitution A C upstream_gene_variant LINC-JP 14 89103623 89103623 single base substitution A G intron_variant LINC-JP 14 89109442 89109442 single base substitution T C intron_variant LINC-JP 14 89123913 89123913 single base substitution G T intron_variant LINC-JP 14 89125586 89125586 deletion of <=200bp T - intron_variant LINC-JP 14 89127113 89127113 single base substitution A G intron_variant LINC-JP 14 89128337 89128337 single base substitution C G intron_variant LINC-JP 14 89129492 89129492 single base substitution A T intron_variant LINC-JP 14 89138786 89138786 single base substitution G A intron_variant LINC-JP 14 89153696 89153696 single base substitution T A intron_variant LINC-JP 14 89153697 89153697 single base substitution A T intron_variant LINC-JP 14 89171823 89171823 single base substitution T C splice_region_variant LINC-JP 14 89172766 89172766 single base substitution G T exon_variant LINC-JP 14 89172766 89172766 single base substitution G T synonymous_variant A554A 1662C>A LINC-JP 14 89178524 89178524 single base substitution T C intron_variant LINC-JP 14 89184900 89184900 single base substitution T C intron_variant LINC-JP 14 89184900 89184900 single base substitution T C upstream_gene_variant LINC-JP 14 89186282 89186282 single base substitution A G intron_variant LINC-JP 14 89186282 89186282 single base substitution A G upstream_gene_variant LINC-JP 14 89188070 89188070 single base substitution A T intron_variant LINC-JP 14 89188076 89188076 single base substitution T G intron_variant LINC-JP 14 89191471 89191471 single base substitution G T intron_variant LINC-JP 14 89205414 89205414 single base substitution T C intron_variant LINC-JP 14 89210334 89210334 deletion of <=200bp C - intron_variant LINC-JP 14 89223904 89223904 single base substitution G T intron_variant LIRI-JP 14 89076802 89076802 single base substitution A G downstream_gene_variant LIRI-JP 14 89077759 89077759 single base substitution A G downstream_gene_variant LIRI-JP 14 89078197 89078197 single base substitution A G downstream_gene_variant LIRI-JP 14 89080384 89080385 deletion of <=200bp TG - 3_prime_UTR_variant LIRI-JP 14 89080384 89080385 deletion of <=200bp TG - downstream_gene_variant LIRI-JP 14 89080384 89080385 deletion of <=200bp TG - exon_variant LIRI-JP 14 89081768 89081768 single base substitution A G 3_prime_UTR_variant LIRI-JP 14 89081768 89081768 single base substitution A G downstream_gene_variant LIRI-JP 14 89081768 89081768 single base substitution A G exon_variant LIRI-JP 14 89082839 89082839 single base substitution G A downstream_gene_variant LIRI-JP 14 89082839 89082839 single base substitution G A intron_variant LIRI-JP 14 89083117 89083117 single base substitution C A 3_prime_UTR_variant LIRI-JP 14 89083117 89083117 single base substitution C A downstream_gene_variant LIRI-JP 14 89083117 89083117 single base substitution C A exon_variant LIRI-JP 14 89083117 89083117 single base substitution C A missense_variant D1871Y 5611G>T LIRI-JP 14 89083117 89083117 single base substitution C A missense_variant D1909Y 5725G>T LIRI-JP 14 89083117 89083117 single base substitution C A missense_variant D1917Y 5749G>T LIRI-JP 14 89085885 89085885 single base substitution T C downstream_gene_variant LIRI-JP 14 89085885 89085885 single base substitution T C exon_variant LIRI-JP 14 89085885 89085885 single base substitution T C intron_variant LIRI-JP 14 89086119 89086119 single base substitution C G downstream_gene_variant LIRI-JP 14 89086119 89086119 single base substitution C G intron_variant LIRI-JP 14 89086119 89086119 single base substitution C G upstream_gene_variant LIRI-JP 14 89092173 89092174 deletion of <=200bp TA - downstream_gene_variant LIRI-JP 14 89092173 89092174 deletion of <=200bp TA - intron_variant LIRI-JP 14 89097425 89097425 single base substitution T C intron_variant LIRI-JP 14 89097425 89097425 single base substitution T C upstream_gene_variant LIRI-JP 14 89098692 89098692 single base substitution C A intron_variant LIRI-JP 14 89100246 89100246 single base substitution T A intron_variant LIRI-JP 14 89105958 89105958 single base substitution T C intron_variant LIRI-JP 14 89114702 89114702 single base substitution T C intron_variant LIRI-JP 14 89114702 89114702 single base substitution T C upstream_gene_variant LIRI-JP 14 89116006 89116006 single base substitution C T intron_variant LIRI-JP 14 89116006 89116006 single base substitution C T upstream_gene_variant LIRI-JP 14 89119025 89119025 single base substitution C A intron_variant LIRI-JP 14 89120390 89120390 single base substitution T C intron_variant LIRI-JP 14 89120814 89120814 single base substitution T C intron_variant LIRI-JP 14 89124735 89124735 single base substitution A G splice_region_variant LIRI-JP 14 89125226 89125226 single base substitution T C intron_variant LIRI-JP 14 89126920 89126920 single base substitution A G intron_variant LIRI-JP 14 89127777 89127777 single base substitution A G intron_variant LIRI-JP 14 89129487 89129487 single base substitution T C intron_variant LIRI-JP 14 89129963 89129963 single base substitution C G intron_variant LIRI-JP 14 89130127 89130127 single base substitution C G intron_variant LIRI-JP 14 89130199 89130199 single base substitution A G intron_variant LIRI-JP 14 89133758 89133758 single base substitution T C intron_variant LIRI-JP 14 89133758 89133758 single base substitution T C upstream_gene_variant LIRI-JP 14 89134688 89134688 single base substitution T C intron_variant LIRI-JP 14 89134688 89134688 single base substitution T C upstream_gene_variant LIRI-JP 14 89135268 89135268 single base substitution C T intron_variant LIRI-JP 14 89135268 89135268 single base substitution C T upstream_gene_variant LIRI-JP 14 89135365 89135365 single base substitution T C intron_variant LIRI-JP 14 89135365 89135365 single base substitution T C upstream_gene_variant LIRI-JP 14 89136342 89136342 single base substitution A T intron_variant LIRI-JP 14 89136342 89136342 single base substitution A T upstream_gene_variant LIRI-JP 14 89138003 89138003 single base substitution C A intron_variant LIRI-JP 14 89138092 89138092 single base substitution A G intron_variant LIRI-JP 14 89142322 89142322 single base substitution C T intron_variant LIRI-JP 14 89143691 89143691 single base substitution A G intron_variant LIRI-JP 14 89146731 89146731 single base substitution C T intron_variant LIRI-JP 14 89146987 89146987 single base substitution T C intron_variant LIRI-JP 14 89150276 89150276 single base substitution T C intron_variant LIRI-JP 14 89150958 89150958 single base substitution C T intron_variant LIRI-JP 14 89151398 89151398 single base substitution T C 3_prime_UTR_variant LIRI-JP 14 89151398 89151398 single base substitution T C synonymous_variant L943L 2829A>G LIRI-JP 14 89151398 89151398 single base substitution T C synonymous_variant L981L 2943A>G LIRI-JP 14 89151705 89151705 single base substitution C G intron_variant LIRI-JP 14 89151726 89151726 single base substitution C T intron_variant LIRI-JP 14 89154744 89154744 single base substitution A G intron_variant LIRI-JP 14 89154744 89154744 single base substitution A G synonymous_variant Y871Y 2613T>C LIRI-JP 14 89157056 89157056 single base substitution T A intron_variant LIRI-JP 14 89157085 89157085 single base substitution T C intron_variant LIRI-JP 14 89157804 89157804 single base substitution G C intron_variant LIRI-JP 14 89160736 89160736 single base substitution C T 3_prime_UTR_variant LIRI-JP 14 89160736 89160736 single base substitution C T synonymous_variant K818K 2454G>A LIRI-JP 14 89160750 89160750 single base substitution C T missense_variant G814R 2440G>A LIRI-JP 14 89160750 89160750 single base substitution C T splice_region_variant LIRI-JP 14 89161163 89161163 single base substitution A G intron_variant LIRI-JP 14 89164594 89164594 single base substitution T C intron_variant LIRI-JP 14 89166216 89166216 single base substitution A T intron_variant LIRI-JP 14 89166496 89166496 single base substitution T A intron_variant LIRI-JP 14 89167879 89167879 single base substitution G T intron_variant LIRI-JP 14 89169000 89169000 deletion of <=200bp A - intron_variant LIRI-JP 14 89170359 89170359 single base substitution T C intron_variant LIRI-JP 14 89170383 89170383 single base substitution G C intron_variant LIRI-JP 14 89173309 89173309 single base substitution T A intron_variant LIRI-JP 14 89174071 89174071 single base substitution T C intron_variant LIRI-JP 14 89175039 89175039 single base substitution G A intron_variant LIRI-JP 14 89176096 89176096 single base substitution G A intron_variant LIRI-JP 14 89177470 89177470 single base substitution A G intron_variant LIRI-JP 14 89177916 89177916 single base substitution C G intron_variant LIRI-JP 14 89180259 89180259 single base substitution G A intron_variant LIRI-JP 14 89183277 89183277 single base substitution C T intron_variant LIRI-JP 14 89183277 89183277 single base substitution C T upstream_gene_variant LIRI-JP 14 89183954 89183954 single base substitution C G intron_variant LIRI-JP 14 89183954 89183954 single base substitution C G upstream_gene_variant LIRI-JP 14 89184267 89184267 single base substitution C T intron_variant LIRI-JP 14 89184267 89184267 single base substitution C T upstream_gene_variant LIRI-JP 14 89184833 89184833 single base substitution A G intron_variant LIRI-JP 14 89184833 89184833 single base substitution A G upstream_gene_variant LIRI-JP 14 89185198 89185198 single base substitution T C intron_variant LIRI-JP 14 89185198 89185198 single base substitution T C upstream_gene_variant LIRI-JP 14 89186667 89186667 single base substitution G T intron_variant LIRI-JP 14 89186812 89186812 single base substitution G T intron_variant LIRI-JP 14 89189046 89189046 single base substitution C A intron_variant LIRI-JP 14 89191788 89191788 single base substitution A C intron_variant LIRI-JP 14 89191988 89191988 single base substitution A T intron_variant LIRI-JP 14 89192308 89192308 single base substitution A G intron_variant LIRI-JP 14 89196259 89196259 single base substitution C G intron_variant LIRI-JP 14 89198766 89198766 single base substitution T C intron_variant LIRI-JP 14 89201131 89201131 single base substitution T C intron_variant LIRI-JP 14 89207318 89207318 single base substitution C A intron_variant LIRI-JP 14 89207319 89207319 single base substitution C A intron_variant LIRI-JP 14 89209057 89209057 single base substitution C A intron_variant LIRI-JP 14 89211647 89211647 single base substitution T C intron_variant LIRI-JP 14 89212073 89212073 single base substitution T A intron_variant LIRI-JP 14 89213825 89213825 single base substitution A G intron_variant LIRI-JP 14 89215750 89215750 single base substitution C T intron_variant LIRI-JP 14 89219327 89219327 single base substitution C T intron_variant LIRI-JP 14 89219635 89219635 single base substitution G A intron_variant LIRI-JP 14 89221455 89221455 single base substitution T C intron_variant LIRI-JP 14 89225529 89225529 single base substitution A G intron_variant LIRI-JP 14 89226706 89226706 single base substitution T G intron_variant LIRI-JP 14 89227957 89227957 single base substitution T G intron_variant LIRI-JP 14 89228572 89228572 single base substitution G A intron_variant LIRI-JP 14 89229030 89229030 single base substitution A G intron_variant LIRI-JP 14 89232701 89232701 single base substitution A G intron_variant LIRI-JP 14 89233606 89233606 single base substitution C T intron_variant LIRI-JP 14 89234091 89234091 single base substitution G A intron_variant LIRI-JP 14 89235347 89235347 single base substitution T C intron_variant LIRI-JP 14 89235616 89235616 single base substitution C A intron_variant LIRI-JP 14 89236067 89236067 single base substitution C T intron_variant LIRI-JP 14 89236791 89236791 single base substitution T C intron_variant LIRI-JP 14 89243201 89243201 single base substitution G C intron_variant LIRI-JP 14 89246441 89246441 single base substitution G A intron_variant LIRI-JP 14 89247215 89247215 single base substitution C T intron_variant LIRI-JP 14 89248962 89248962 single base substitution C G intron_variant LIRI-JP 14 89253048 89253048 single base substitution G A intron_variant LIRI-JP 14 89254716 89254716 single base substitution T C intron_variant LIRI-JP 14 89255198 89255198 single base substitution C A intron_variant LIRI-JP 14 89255199 89255199 single base substitution C A intron_variant LIRI-JP 14 89256959 89256959 single base substitution A G intron_variant LIRI-JP 14 89257594 89257594 single base substitution T C intron_variant LIRI-JP 14 89257597 89257597 single base substitution T G intron_variant LIRI-JP 14 89259545 89259545 single base substitution A G upstream_gene_variant LUSC-KR 14 89076056 89076056 single base substitution C T downstream_gene_variant LUSC-KR 14 89094939 89094939 single base substitution C T intron_variant LUSC-KR 14 89094939 89094939 single base substitution C T upstream_gene_variant LUSC-KR 14 89097583 89097583 single base substitution G T intron_variant LUSC-KR 14 89097583 89097583 single base substitution G T upstream_gene_variant LUSC-KR 14 89100642 89100642 single base substitution T C intron_variant LUSC-KR 14 89101317 89101317 single base substitution G A intron_variant LUSC-KR 14 89101348 89101348 single base substitution C G intron_variant LUSC-KR 14 89103963 89103963 single base substitution C G intron_variant LUSC-KR 14 89105962 89105962 single base substitution C G intron_variant LUSC-KR 14 89107251 89107251 single base substitution C A intron_variant LUSC-KR 14 89108375 89108375 single base substitution C A intron_variant LUSC-KR 14 89113282 89113282 single base substitution G A intron_variant LUSC-KR 14 89113282 89113282 single base substitution G A upstream_gene_variant LUSC-KR 14 89115561 89115561 single base substitution G T intron_variant LUSC-KR 14 89115561 89115561 single base substitution G T upstream_gene_variant LUSC-KR 14 89118570 89118570 single base substitution C G intron_variant LUSC-KR 14 89125154 89125154 single base substitution C A intron_variant LUSC-KR 14 89125185 89125185 single base substitution A G intron_variant LUSC-KR 14 89125467 89125467 single base substitution C G intron_variant LUSC-KR 14 89126336 89126336 single base substitution C A intron_variant LUSC-KR 14 89129370 89129370 single base substitution C T splice_region_variant LUSC-KR 14 89130094 89130094 single base substitution G T intron_variant LUSC-KR 14 89130635 89130635 single base substitution G A intron_variant LUSC-KR 14 89130640 89130640 single base substitution G A intron_variant LUSC-KR 14 89130653 89130653 single base substitution G A intron_variant LUSC-KR 14 89131585 89131585 single base substitution T A intron_variant LUSC-KR 14 89132941 89132941 single base substitution C T intron_variant LUSC-KR 14 89132941 89132941 single base substitution C T upstream_gene_variant LUSC-KR 14 89135181 89135181 single base substitution G T intron_variant LUSC-KR 14 89135181 89135181 single base substitution G T upstream_gene_variant LUSC-KR 14 89139534 89139534 single base substitution G T intron_variant LUSC-KR 14 89140161 89140161 single base substitution C T intron_variant LUSC-KR 14 89145405 89145405 single base substitution T A intron_variant LUSC-KR 14 89150473 89150473 single base substitution A T intron_variant LUSC-KR 14 89152092 89152092 single base substitution C A intron_variant LUSC-KR 14 89156266 89156266 single base substitution G T intron_variant LUSC-KR 14 89160659 89160659 single base substitution C A 3_prime_UTR_variant LUSC-KR 14 89160659 89160659 single base substitution C A missense_variant R844L 2531G>T LUSC-KR 14 89163599 89163599 single base substitution A T intron_variant LUSC-KR 14 89170682 89170682 single base substitution G C intron_variant LUSC-KR 14 89172035 89172035 single base substitution C A intron_variant LUSC-KR 14 89172364 89172364 single base substitution C A intron_variant LUSC-KR 14 89172700 89172700 single base substitution C A exon_variant LUSC-KR 14 89172700 89172700 single base substitution C A missense_variant Q576H 1728G>T LUSC-KR 14 89176983 89176983 single base substitution T C intron_variant LUSC-KR 14 89177193 89177193 single base substitution A T intron_variant LUSC-KR 14 89177746 89177746 single base substitution C A intron_variant LUSC-KR 14 89179515 89179515 single base substitution C A intron_variant LUSC-KR 14 89179913 89179913 single base substitution C G intron_variant LUSC-KR 14 89181559 89181559 single base substitution G A intron_variant LUSC-KR 14 89181559 89181559 single base substitution G A upstream_gene_variant LUSC-KR 14 89192517 89192517 single base substitution C G intron_variant LUSC-KR 14 89193559 89193559 single base substitution T A intron_variant LUSC-KR 14 89196307 89196307 single base substitution G A intron_variant LUSC-KR 14 89197655 89197655 single base substitution C A intron_variant LUSC-KR 14 89197724 89197724 single base substitution C A intron_variant LUSC-KR 14 89198328 89198328 single base substitution G C intron_variant LUSC-KR 14 89199777 89199777 single base substitution C T intron_variant LUSC-KR 14 89205576 89205576 single base substitution G C intron_variant LUSC-KR 14 89206792 89206792 single base substitution T C missense_variant N217S 650A>G LUSC-KR 14 89207485 89207485 single base substitution C A intron_variant LUSC-KR 14 89211515 89211515 single base substitution G T intron_variant LUSC-KR 14 89211519 89211519 single base substitution G T intron_variant LUSC-KR 14 89214201 89214201 single base substitution G T intron_variant LUSC-KR 14 89214202 89214202 single base substitution G T intron_variant LUSC-KR 14 89214638 89214638 single base substitution A C intron_variant LUSC-KR 14 89218023 89218023 single base substitution C G intron_variant LUSC-KR 14 89220599 89220599 single base substitution T G intron_variant LUSC-KR 14 89222891 89222891 single base substitution T C intron_variant LUSC-KR 14 89223641 89223641 single base substitution C A intron_variant LUSC-KR 14 89225856 89225856 single base substitution C A intron_variant LUSC-KR 14 89230893 89230893 single base substitution C A intron_variant LUSC-KR 14 89236484 89236484 single base substitution T C intron_variant LUSC-KR 14 89239330 89239330 single base substitution G A intron_variant LUSC-KR 14 89239975 89239975 single base substitution A T intron_variant LUSC-KR 14 89240364 89240364 single base substitution G T intron_variant LUSC-KR 14 89246300 89246300 single base substitution A T intron_variant LUSC-KR 14 89249507 89249507 single base substitution C A intron_variant LUSC-KR 14 89249988 89249988 single base substitution T A intron_variant LUSC-KR 14 89250402 89250402 single base substitution C T intron_variant LUSC-KR 14 89258941 89258941 single base substitution G C 5_prime_UTR_variant LUSC-KR 14 89258941 89258941 single base substitution G C upstream_gene_variant LUSC-KR 14 89259648 89259648 single base substitution G T upstream_gene_variant LUSC-US 14 89087225 89087225 single base substitution A G 3_prime_UTR_variant LUSC-US 14 89087225 89087225 single base substitution A G downstream_gene_variant LUSC-US 14 89087225 89087225 single base substitution A G missense_variant C1704R 5110T>C LUSC-US 14 89087225 89087225 single base substitution A G missense_variant C1742R 5224T>C LUSC-US 14 89087225 89087225 single base substitution A G missense_variant C1750R 5248T>C LUSC-US 14 89087225 89087225 single base substitution A G missense_variant C190R 568T>C LUSC-US 14 89087225 89087225 single base substitution A G upstream_gene_variant LUSC-US 14 89105221 89105221 single base substitution T C 3_prime_UTR_variant LUSC-US 14 89105221 89105221 single base substitution T C exon_variant LUSC-US 14 89105221 89105221 single base substitution T C missense_variant D1377G 4130A>G LUSC-US 14 89105221 89105221 single base substitution T C missense_variant D1415G 4244A>G LUSC-US 14 89105221 89105221 single base substitution T C missense_variant D1423G 4268A>G LUSC-US 14 89123748 89123748 single base substitution G A 3_prime_UTR_variant LUSC-US 14 89123748 89123748 single base substitution G A stop_gained Q1288* 3862C>T LUSC-US 14 89123748 89123748 single base substitution G A stop_gained Q1326* 3976C>T LUSC-US 14 89154734 89154734 single base substitution C T intron_variant LUSC-US 14 89154734 89154734 single base substitution C T missense_variant E875K 2623G>A LUSC-US 14 89163203 89163203 single base substitution C A 3_prime_UTR_variant LUSC-US 14 89163203 89163203 single base substitution C A missense_variant V778F 2332G>T LUSC-US 14 89168804 89168804 single base substitution C G 3_prime_UTR_variant LUSC-US 14 89168804 89168804 single base substitution C G missense_variant V742L 2224G>C LUSC-US 14 89181371 89181371 single base substitution A G exon_variant LUSC-US 14 89181371 89181371 single base substitution A G synonymous_variant S452S 1356T>C LUSC-US 14 89181377 89181377 single base substitution G A exon_variant LUSC-US 14 89181377 89181377 single base substitution G A synonymous_variant S450S 1350C>T LUSC-US 14 89192897 89192897 single base substitution A G missense_variant V392A 1175T>C LUSC-US 14 89202760 89202760 single base substitution C A missense_variant V333F 997G>T MALY-DE 14 89075086 89075086 single base substitution A G downstream_gene_variant MALY-DE 14 89078400 89078400 single base substitution T G downstream_gene_variant MALY-DE 14 89078782 89078782 single base substitution C G 3_prime_UTR_variant MALY-DE 14 89078782 89078782 single base substitution C G downstream_gene_variant MALY-DE 14 89079498 89079498 single base substitution T C 3_prime_UTR_variant MALY-DE 14 89079498 89079498 single base substitution T C downstream_gene_variant MALY-DE 14 89079937 89079937 single base substitution A G 3_prime_UTR_variant MALY-DE 14 89079937 89079937 single base substitution A G downstream_gene_variant MALY-DE 14 89085603 89085603 single base substitution G A downstream_gene_variant MALY-DE 14 89085603 89085603 single base substitution G A exon_variant MALY-DE 14 89085603 89085603 single base substitution G A intron_variant MALY-DE 14 89089467 89089467 single base substitution C T downstream_gene_variant MALY-DE 14 89089467 89089467 single base substitution C T intron_variant MALY-DE 14 89089467 89089467 single base substitution C T upstream_gene_variant MALY-DE 14 89090877 89090877 single base substitution A G downstream_gene_variant MALY-DE 14 89090877 89090877 single base substitution A G intron_variant MALY-DE 14 89090877 89090877 single base substitution A G upstream_gene_variant MALY-DE 14 89093961 89093961 single base substitution T A downstream_gene_variant MALY-DE 14 89093961 89093961 single base substitution T A intron_variant MALY-DE 14 89093961 89093961 single base substitution T A upstream_gene_variant MALY-DE 14 89095038 89095038 single base substitution A C intron_variant MALY-DE 14 89095038 89095038 single base substitution A C upstream_gene_variant MALY-DE 14 89095057 89095057 single base substitution A G intron_variant MALY-DE 14 89095057 89095057 single base substitution A G upstream_gene_variant MALY-DE 14 89095118 89095118 single base substitution A T intron_variant MALY-DE 14 89095118 89095118 single base substitution A T upstream_gene_variant MALY-DE 14 89095165 89095165 single base substitution G C intron_variant MALY-DE 14 89095165 89095165 single base substitution G C upstream_gene_variant MALY-DE 14 89103363 89103363 single base substitution C T intron_variant MALY-DE 14 89113344 89113344 single base substitution T G intron_variant MALY-DE 14 89113344 89113344 single base substitution T G upstream_gene_variant MALY-DE 14 89116297 89116297 single base substitution G A intron_variant MALY-DE 14 89117707 89117707 single base substitution A G intron_variant MALY-DE 14 89126974 89126974 single base substitution C A intron_variant MALY-DE 14 89127090 89127090 single base substitution A G intron_variant MALY-DE 14 89130073 89130073 single base substitution C T intron_variant MALY-DE 14 89132745 89132745 single base substitution T C intron_variant MALY-DE 14 89132745 89132745 single base substitution T C upstream_gene_variant MALY-DE 14 89134098 89134098 single base substitution A T intron_variant MALY-DE 14 89134098 89134098 single base substitution A T upstream_gene_variant MALY-DE 14 89136399 89136399 single base substitution C G intron_variant MALY-DE 14 89136399 89136399 single base substitution C G upstream_gene_variant MALY-DE 14 89140387 89140387 single base substitution C T intron_variant MALY-DE 14 89141138 89141138 single base substitution A C intron_variant MALY-DE 14 89141712 89141712 single base substitution G T intron_variant MALY-DE 14 89163491 89163491 single base substitution C T intron_variant MALY-DE 14 89163635 89163635 single base substitution A C intron_variant MALY-DE 14 89167301 89167301 single base substitution T G intron_variant MALY-DE 14 89173353 89173353 single base substitution C T intron_variant MALY-DE 14 89173837 89173837 single base substitution T G intron_variant MALY-DE 14 89175173 89175173 single base substitution A C intron_variant MALY-DE 14 89178593 89178593 single base substitution A C intron_variant MALY-DE 14 89180196 89180196 single base substitution T A intron_variant MALY-DE 14 89185753 89185753 single base substitution T G intron_variant MALY-DE 14 89185753 89185753 single base substitution T G upstream_gene_variant MALY-DE 14 89186018 89186018 deletion of <=200bp T - intron_variant MALY-DE 14 89186018 89186018 deletion of <=200bp T - upstream_gene_variant MALY-DE 14 89186710 89186710 single base substitution A C intron_variant MALY-DE 14 89187256 89187256 single base substitution A C intron_variant MALY-DE 14 89189703 89189704 deletion of <=200bp AC - intron_variant MALY-DE 14 89189716 89189716 single base substitution G A intron_variant MALY-DE 14 89199094 89199094 single base substitution A C intron_variant MALY-DE 14 89205177 89205177 single base substitution G A intron_variant MALY-DE 14 89206313 89206313 insertion of <=200bp - A intron_variant MALY-DE 14 89206407 89206407 single base substitution A T intron_variant MALY-DE 14 89207819 89207819 single base substitution A G intron_variant MALY-DE 14 89229957 89229957 single base substitution T C intron_variant MALY-DE 14 89230825 89230825 single base substitution T C intron_variant MALY-DE 14 89233982 89233982 single base substitution G C intron_variant MALY-DE 14 89235689 89235689 single base substitution T C intron_variant MALY-DE 14 89237835 89237835 single base substitution T G intron_variant MALY-DE 14 89238468 89238468 single base substitution C G intron_variant MALY-DE 14 89244297 89244297 single base substitution C T intron_variant MALY-DE 14 89248042 89248042 single base substitution A T intron_variant MALY-DE 14 89249677 89249677 single base substitution C A intron_variant MALY-DE 14 89249797 89249797 single base substitution G A intron_variant MALY-DE 14 89250665 89250665 single base substitution A T intron_variant MALY-DE 14 89251943 89251943 single base substitution G T intron_variant MALY-DE 14 89252080 89252080 single base substitution C G intron_variant MALY-DE 14 89253346 89253346 single base substitution G A intron_variant MALY-DE 14 89254224 89254224 single base substitution C T intron_variant MALY-DE 14 89254876 89254876 single base substitution A T intron_variant MALY-DE 14 89259023 89259023 single base substitution G A 5_prime_UTR_variant MALY-DE 14 89259023 89259023 single base substitution G A upstream_gene_variant MELA-AU 14 89075878 89075878 single base substitution C T downstream_gene_variant MELA-AU 14 89076260 89076260 single base substitution C T downstream_gene_variant MELA-AU 14 89076347 89076348 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 14 89076768 89076768 single base substitution C T downstream_gene_variant MELA-AU 14 89076985 89076985 single base substitution C T downstream_gene_variant MELA-AU 14 89077559 89077559 single base substitution C T downstream_gene_variant MELA-AU 14 89077693 89077693 single base substitution C T downstream_gene_variant MELA-AU 14 89078596 89078596 single base substitution T C downstream_gene_variant MELA-AU 14 89079052 89079052 single base substitution A C 3_prime_UTR_variant MELA-AU 14 89079052 89079052 single base substitution A C downstream_gene_variant MELA-AU 14 89080518 89080518 single base substitution T C 3_prime_UTR_variant MELA-AU 14 89080518 89080518 single base substitution T C downstream_gene_variant MELA-AU 14 89080518 89080518 single base substitution T C exon_variant MELA-AU 14 89081374 89081374 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89081374 89081374 single base substitution C T downstream_gene_variant MELA-AU 14 89081374 89081374 single base substitution C T exon_variant MELA-AU 14 89081647 89081647 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89081647 89081647 single base substitution C T downstream_gene_variant MELA-AU 14 89081647 89081647 single base substitution C T exon_variant MELA-AU 14 89081784 89081784 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89081784 89081784 single base substitution C T downstream_gene_variant MELA-AU 14 89081784 89081784 single base substitution C T exon_variant MELA-AU 14 89081985 89081985 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89081985 89081985 single base substitution C T downstream_gene_variant MELA-AU 14 89081985 89081985 single base substitution C T exon_variant MELA-AU 14 89083690 89083690 single base substitution C T downstream_gene_variant MELA-AU 14 89083690 89083690 single base substitution C T intron_variant MELA-AU 14 89083749 89083749 single base substitution C T downstream_gene_variant MELA-AU 14 89083749 89083749 single base substitution C T intron_variant MELA-AU 14 89084705 89084705 single base substitution A T downstream_gene_variant MELA-AU 14 89084705 89084705 single base substitution A T intron_variant MELA-AU 14 89085414 89085414 single base substitution A C downstream_gene_variant MELA-AU 14 89085414 89085414 single base substitution A C exon_variant MELA-AU 14 89085414 89085414 single base substitution A C intron_variant MELA-AU 14 89086003 89086003 single base substitution G A downstream_gene_variant MELA-AU 14 89086003 89086003 single base substitution G A exon_variant MELA-AU 14 89086003 89086003 single base substitution G A intron_variant MELA-AU 14 89086669 89086669 single base substitution T G downstream_gene_variant MELA-AU 14 89086669 89086669 single base substitution T G intron_variant MELA-AU 14 89086669 89086669 single base substitution T G upstream_gene_variant MELA-AU 14 89087180 89087180 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89087180 89087180 single base substitution C T downstream_gene_variant MELA-AU 14 89087180 89087180 single base substitution C T missense_variant G1719R 5155G>A MELA-AU 14 89087180 89087180 single base substitution C T missense_variant G1757R 5269G>A MELA-AU 14 89087180 89087180 single base substitution C T missense_variant G1765R 5293G>A MELA-AU 14 89087180 89087180 single base substitution C T missense_variant G205R 613G>A MELA-AU 14 89087180 89087180 single base substitution C T upstream_gene_variant MELA-AU 14 89088611 89088612 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89088611 89088612 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 14 89089099 89089099 single base substitution T C downstream_gene_variant MELA-AU 14 89089099 89089099 single base substitution T C intron_variant MELA-AU 14 89089099 89089099 single base substitution T C upstream_gene_variant MELA-AU 14 89089479 89089480 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 14 89089479 89089480 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89089479 89089480 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 14 89090097 89090097 single base substitution C T downstream_gene_variant MELA-AU 14 89090097 89090097 single base substitution C T intron_variant MELA-AU 14 89090097 89090097 single base substitution C T upstream_gene_variant MELA-AU 14 89090811 89090811 single base substitution G A downstream_gene_variant MELA-AU 14 89090811 89090811 single base substitution G A intron_variant MELA-AU 14 89090811 89090811 single base substitution G A upstream_gene_variant MELA-AU 14 89091113 89091113 single base substitution A T downstream_gene_variant MELA-AU 14 89091113 89091113 single base substitution A T intron_variant MELA-AU 14 89091778 89091778 single base substitution C T downstream_gene_variant MELA-AU 14 89091778 89091778 single base substitution C T intron_variant MELA-AU 14 89093301 89093301 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89093301 89093301 single base substitution C T downstream_gene_variant MELA-AU 14 89093301 89093301 single base substitution C T missense_variant G1495R 4483G>A MELA-AU 14 89093301 89093301 single base substitution C T missense_variant G1533R 4597G>A MELA-AU 14 89093301 89093301 single base substitution C T missense_variant G1541R 4621G>A MELA-AU 14 89093301 89093301 single base substitution C T upstream_gene_variant MELA-AU 14 89093597 89093597 single base substitution T C downstream_gene_variant MELA-AU 14 89093597 89093597 single base substitution T C intron_variant MELA-AU 14 89093597 89093597 single base substitution T C upstream_gene_variant MELA-AU 14 89093778 89093778 single base substitution G A downstream_gene_variant MELA-AU 14 89093778 89093778 single base substitution G A intron_variant MELA-AU 14 89093778 89093778 single base substitution G A upstream_gene_variant MELA-AU 14 89093990 89093990 single base substitution C T downstream_gene_variant MELA-AU 14 89093990 89093990 single base substitution C T missense_variant G1465S 4393G>A MELA-AU 14 89093990 89093990 single base substitution C T missense_variant G1503S 4507G>A MELA-AU 14 89093990 89093990 single base substitution C T missense_variant G1511S 4531G>A MELA-AU 14 89093990 89093990 single base substitution C T splice_region_variant MELA-AU 14 89093990 89093990 single base substitution C T upstream_gene_variant MELA-AU 14 89094004 89094004 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89094004 89094004 single base substitution C T downstream_gene_variant MELA-AU 14 89094004 89094004 single base substitution C T stop_gained W1460* 4379G>A MELA-AU 14 89094004 89094004 single base substitution C T stop_gained W1498* 4493G>A MELA-AU 14 89094004 89094004 single base substitution C T stop_gained W1506* 4517G>A MELA-AU 14 89094004 89094004 single base substitution C T upstream_gene_variant MELA-AU 14 89094359 89094359 single base substitution G A intron_variant MELA-AU 14 89094359 89094359 single base substitution G A upstream_gene_variant MELA-AU 14 89095107 89095107 single base substitution T A intron_variant MELA-AU 14 89095107 89095107 single base substitution T A upstream_gene_variant MELA-AU 14 89095200 89095200 single base substitution T A intron_variant MELA-AU 14 89095200 89095200 single base substitution T A upstream_gene_variant MELA-AU 14 89096028 89096028 single base substitution T A intron_variant MELA-AU 14 89096028 89096028 single base substitution T A upstream_gene_variant MELA-AU 14 89096209 89096209 single base substitution C T intron_variant MELA-AU 14 89096209 89096209 single base substitution C T upstream_gene_variant MELA-AU 14 89096216 89096216 single base substitution A C intron_variant MELA-AU 14 89096216 89096216 single base substitution A C upstream_gene_variant MELA-AU 14 89096488 89096488 single base substitution C T intron_variant MELA-AU 14 89096488 89096488 single base substitution C T upstream_gene_variant MELA-AU 14 89096893 89096893 single base substitution C T intron_variant MELA-AU 14 89096893 89096893 single base substitution C T upstream_gene_variant MELA-AU 14 89096929 89096929 single base substitution C T intron_variant MELA-AU 14 89096929 89096929 single base substitution C T upstream_gene_variant MELA-AU 14 89097067 89097067 single base substitution G A intron_variant MELA-AU 14 89097067 89097067 single base substitution G A upstream_gene_variant MELA-AU 14 89097082 89097082 single base substitution C T intron_variant MELA-AU 14 89097082 89097082 single base substitution C T upstream_gene_variant MELA-AU 14 89097271 89097271 single base substitution C T intron_variant MELA-AU 14 89097271 89097271 single base substitution C T upstream_gene_variant MELA-AU 14 89097652 89097652 single base substitution G A intron_variant MELA-AU 14 89097652 89097652 single base substitution G A upstream_gene_variant MELA-AU 14 89097871 89097871 single base substitution G A intron_variant MELA-AU 14 89097871 89097871 single base substitution G A upstream_gene_variant MELA-AU 14 89098403 89098404 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89098427 89098427 single base substitution C T intron_variant MELA-AU 14 89098862 89098862 single base substitution G A intron_variant MELA-AU 14 89100075 89100075 single base substitution C T intron_variant MELA-AU 14 89100262 89100262 single base substitution A C intron_variant MELA-AU 14 89100456 89100456 single base substitution G A intron_variant MELA-AU 14 89100474 89100474 single base substitution C T intron_variant MELA-AU 14 89100786 89100786 single base substitution A C intron_variant MELA-AU 14 89100808 89100808 single base substitution C T intron_variant MELA-AU 14 89100808 89100808 single base substitution C T splice_region_variant MELA-AU 14 89101246 89101246 single base substitution G A intron_variant MELA-AU 14 89101246 89101246 single base substitution G C intron_variant MELA-AU 14 89101287 89101287 single base substitution G A intron_variant MELA-AU 14 89101315 89101315 single base substitution G T intron_variant MELA-AU 14 89101575 89101575 single base substitution G A intron_variant MELA-AU 14 89101683 89101683 single base substitution G A intron_variant MELA-AU 14 89102563 89102563 single base substitution G T intron_variant MELA-AU 14 89102656 89102656 single base substitution C T intron_variant MELA-AU 14 89103077 89103077 single base substitution G A intron_variant MELA-AU 14 89103319 89103319 single base substitution G A intron_variant MELA-AU 14 89104009 89104009 single base substitution G A intron_variant MELA-AU 14 89104029 89104029 single base substitution A T intron_variant MELA-AU 14 89104091 89104091 single base substitution C T intron_variant MELA-AU 14 89104102 89104102 single base substitution G A intron_variant MELA-AU 14 89104402 89104402 single base substitution G A intron_variant MELA-AU 14 89104438 89104438 single base substitution A C intron_variant MELA-AU 14 89104699 89104699 single base substitution G A intron_variant MELA-AU 14 89104740 89104740 single base substitution C T intron_variant MELA-AU 14 89104897 89104897 single base substitution A G intron_variant MELA-AU 14 89104944 89104944 single base substitution G A intron_variant MELA-AU 14 89105041 89105041 single base substitution G A intron_variant MELA-AU 14 89105446 89105446 single base substitution G A intron_variant MELA-AU 14 89105563 89105563 single base substitution G A intron_variant MELA-AU 14 89105654 89105654 single base substitution G A intron_variant MELA-AU 14 89105783 89105783 single base substitution C G intron_variant MELA-AU 14 89105787 89105787 single base substitution C T intron_variant MELA-AU 14 89105806 89105806 single base substitution A G intron_variant MELA-AU 14 89105809 89105809 single base substitution G A intron_variant MELA-AU 14 89106011 89106011 single base substitution C T intron_variant MELA-AU 14 89106140 89106140 single base substitution G A intron_variant MELA-AU 14 89106226 89106226 single base substitution G A intron_variant MELA-AU 14 89106325 89106325 single base substitution G A intron_variant MELA-AU 14 89106859 89106859 single base substitution G A intron_variant MELA-AU 14 89107016 89107016 single base substitution A G intron_variant MELA-AU 14 89107301 89107301 single base substitution G A intron_variant MELA-AU 14 89107417 89107417 single base substitution C T intron_variant MELA-AU 14 89107539 89107539 single base substitution G A intron_variant MELA-AU 14 89107575 89107575 single base substitution G C intron_variant MELA-AU 14 89107798 89107798 single base substitution C T intron_variant MELA-AU 14 89107940 89107940 single base substitution G A intron_variant MELA-AU 14 89108027 89108027 single base substitution G A intron_variant MELA-AU 14 89108299 89108299 single base substitution G A intron_variant MELA-AU 14 89108434 89108434 single base substitution C T intron_variant MELA-AU 14 89108583 89108583 single base substitution A G intron_variant MELA-AU 14 89108642 89108642 single base substitution G A intron_variant MELA-AU 14 89108743 89108743 single base substitution C T intron_variant MELA-AU 14 89109059 89109059 single base substitution G A intron_variant MELA-AU 14 89109102 89109102 single base substitution G A intron_variant MELA-AU 14 89109574 89109574 single base substitution C T intron_variant MELA-AU 14 89109709 89109709 single base substitution G A intron_variant MELA-AU 14 89109964 89109965 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89110027 89110027 single base substitution G A intron_variant MELA-AU 14 89110200 89110200 single base substitution G A intron_variant MELA-AU 14 89110384 89110384 single base substitution A G intron_variant MELA-AU 14 89110414 89110414 single base substitution C T intron_variant MELA-AU 14 89110486 89110486 single base substitution C G intron_variant MELA-AU 14 89111104 89111104 single base substitution G A intron_variant MELA-AU 14 89111104 89111104 single base substitution G A upstream_gene_variant MELA-AU 14 89111158 89111158 single base substitution G A intron_variant MELA-AU 14 89111158 89111158 single base substitution G A upstream_gene_variant MELA-AU 14 89111291 89111292 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89111291 89111292 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 14 89111463 89111463 single base substitution G A intron_variant MELA-AU 14 89111463 89111463 single base substitution G A upstream_gene_variant MELA-AU 14 89111875 89111875 single base substitution G A intron_variant MELA-AU 14 89111875 89111875 single base substitution G A upstream_gene_variant MELA-AU 14 89111882 89111882 single base substitution C T intron_variant MELA-AU 14 89111882 89111882 single base substitution C T upstream_gene_variant MELA-AU 14 89112088 89112088 single base substitution G A intron_variant MELA-AU 14 89112088 89112088 single base substitution G A upstream_gene_variant MELA-AU 14 89112202 89112202 single base substitution C T intron_variant MELA-AU 14 89112202 89112202 single base substitution C T upstream_gene_variant MELA-AU 14 89112776 89112776 single base substitution C T intron_variant MELA-AU 14 89112776 89112776 single base substitution C T upstream_gene_variant MELA-AU 14 89112843 89112843 single base substitution C T intron_variant MELA-AU 14 89112843 89112843 single base substitution C T upstream_gene_variant MELA-AU 14 89113080 89113080 single base substitution G A intron_variant MELA-AU 14 89113080 89113080 single base substitution G A upstream_gene_variant MELA-AU 14 89113130 89113130 single base substitution G A intron_variant MELA-AU 14 89113130 89113130 single base substitution G A upstream_gene_variant MELA-AU 14 89113164 89113164 single base substitution G A intron_variant MELA-AU 14 89113164 89113164 single base substitution G A upstream_gene_variant MELA-AU 14 89113502 89113502 single base substitution C T intron_variant MELA-AU 14 89113502 89113502 single base substitution C T upstream_gene_variant MELA-AU 14 89113635 89113635 single base substitution G A intron_variant MELA-AU 14 89113635 89113635 single base substitution G A upstream_gene_variant MELA-AU 14 89113946 89113946 single base substitution G A intron_variant MELA-AU 14 89113946 89113946 single base substitution G A upstream_gene_variant MELA-AU 14 89114017 89114017 single base substitution G A intron_variant MELA-AU 14 89114017 89114017 single base substitution G A upstream_gene_variant MELA-AU 14 89114138 89114138 single base substitution C T intron_variant MELA-AU 14 89114138 89114138 single base substitution C T upstream_gene_variant MELA-AU 14 89114146 89114146 single base substitution G A intron_variant MELA-AU 14 89114146 89114146 single base substitution G A upstream_gene_variant MELA-AU 14 89114177 89114177 single base substitution G A intron_variant MELA-AU 14 89114177 89114177 single base substitution G A upstream_gene_variant MELA-AU 14 89114290 89114290 single base substitution G A intron_variant MELA-AU 14 89114290 89114290 single base substitution G A upstream_gene_variant MELA-AU 14 89114509 89114509 single base substitution A C intron_variant MELA-AU 14 89114509 89114509 single base substitution A C upstream_gene_variant MELA-AU 14 89114768 89114768 single base substitution G A intron_variant MELA-AU 14 89114768 89114768 single base substitution G A upstream_gene_variant MELA-AU 14 89114833 89114833 single base substitution G A intron_variant MELA-AU 14 89114833 89114833 single base substitution G A upstream_gene_variant MELA-AU 14 89115023 89115023 single base substitution G A intron_variant MELA-AU 14 89115023 89115023 single base substitution G A upstream_gene_variant MELA-AU 14 89115322 89115322 single base substitution G A intron_variant MELA-AU 14 89115322 89115322 single base substitution G A upstream_gene_variant MELA-AU 14 89115390 89115390 single base substitution C T intron_variant MELA-AU 14 89115390 89115390 single base substitution C T upstream_gene_variant MELA-AU 14 89115676 89115676 single base substitution G A intron_variant MELA-AU 14 89115676 89115676 single base substitution G A upstream_gene_variant MELA-AU 14 89115950 89115950 single base substitution G A intron_variant MELA-AU 14 89115950 89115950 single base substitution G A upstream_gene_variant MELA-AU 14 89116456 89116456 single base substitution G A intron_variant MELA-AU 14 89116943 89116943 single base substitution G A intron_variant MELA-AU 14 89117008 89117008 single base substitution G A intron_variant MELA-AU 14 89117546 89117546 single base substitution C T intron_variant MELA-AU 14 89118187 89118187 single base substitution C T intron_variant MELA-AU 14 89118196 89118196 single base substitution G A intron_variant MELA-AU 14 89118263 89118263 single base substitution G A intron_variant MELA-AU 14 89118425 89118425 single base substitution G A intron_variant MELA-AU 14 89118458 89118458 single base substitution G A intron_variant MELA-AU 14 89118821 89118821 single base substitution C T intron_variant MELA-AU 14 89118834 89118834 single base substitution C T intron_variant MELA-AU 14 89118921 89118921 single base substitution C T intron_variant MELA-AU 14 89119059 89119059 single base substitution C T intron_variant MELA-AU 14 89119192 89119192 single base substitution C G intron_variant MELA-AU 14 89119238 89119238 single base substitution G A intron_variant MELA-AU 14 89119263 89119263 single base substitution T G intron_variant MELA-AU 14 89119264 89119264 single base substitution C T intron_variant MELA-AU 14 89119323 89119323 single base substitution C T intron_variant MELA-AU 14 89119451 89119451 single base substitution G A intron_variant MELA-AU 14 89119470 89119470 single base substitution G A intron_variant MELA-AU 14 89119612 89119612 single base substitution C T intron_variant MELA-AU 14 89119965 89119965 single base substitution G A intron_variant MELA-AU 14 89120093 89120093 single base substitution G A intron_variant MELA-AU 14 89120101 89120101 single base substitution C T intron_variant MELA-AU 14 89120141 89120141 single base substitution G A intron_variant MELA-AU 14 89120167 89120167 single base substitution G A intron_variant MELA-AU 14 89120239 89120239 single base substitution A G intron_variant MELA-AU 14 89120246 89120246 single base substitution G A intron_variant MELA-AU 14 89120624 89120624 single base substitution C A intron_variant MELA-AU 14 89120946 89120946 single base substitution C T intron_variant MELA-AU 14 89121068 89121068 single base substitution T A intron_variant MELA-AU 14 89121087 89121087 single base substitution G A intron_variant MELA-AU 14 89121169 89121169 single base substitution G A intron_variant MELA-AU 14 89121276 89121276 single base substitution G A intron_variant MELA-AU 14 89121464 89121464 single base substitution G A intron_variant MELA-AU 14 89121657 89121657 single base substitution G A intron_variant MELA-AU 14 89121864 89121864 single base substitution A T intron_variant MELA-AU 14 89122177 89122177 single base substitution G A intron_variant MELA-AU 14 89122489 89122489 single base substitution C T intron_variant MELA-AU 14 89122741 89122741 single base substitution C T intron_variant MELA-AU 14 89122773 89122773 single base substitution G A intron_variant MELA-AU 14 89122833 89122833 single base substitution G A intron_variant MELA-AU 14 89123083 89123083 single base substitution G A intron_variant MELA-AU 14 89123739 89123739 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89123739 89123739 single base substitution C T missense_variant E1291K 3871G>A MELA-AU 14 89123739 89123739 single base substitution C T missense_variant E1329K 3985G>A MELA-AU 14 89123992 89123992 single base substitution G A intron_variant MELA-AU 14 89124266 89124266 single base substitution G A intron_variant MELA-AU 14 89124556 89124556 single base substitution G A 3_prime_UTR_variant MELA-AU 14 89124556 89124556 single base substitution G A synonymous_variant S1246S 3738C>T MELA-AU 14 89124556 89124556 single base substitution G A synonymous_variant S1284S 3852C>T MELA-AU 14 89124790 89124790 single base substitution C T intron_variant MELA-AU 14 89124797 89124797 single base substitution G A intron_variant MELA-AU 14 89125393 89125393 single base substitution C T intron_variant MELA-AU 14 89125529 89125529 single base substitution C T intron_variant MELA-AU 14 89125572 89125572 single base substitution G A intron_variant MELA-AU 14 89126005 89126005 single base substitution G A intron_variant MELA-AU 14 89126033 89126033 single base substitution G A intron_variant MELA-AU 14 89126386 89126386 single base substitution G A intron_variant MELA-AU 14 89126612 89126612 single base substitution G C intron_variant MELA-AU 14 89126663 89126663 single base substitution G A intron_variant MELA-AU 14 89127088 89127088 single base substitution G A intron_variant MELA-AU 14 89127135 89127135 single base substitution G A intron_variant MELA-AU 14 89127237 89127237 single base substitution G A intron_variant MELA-AU 14 89127517 89127517 single base substitution C T intron_variant MELA-AU 14 89127567 89127567 single base substitution G A intron_variant MELA-AU 14 89127782 89127782 single base substitution G A intron_variant MELA-AU 14 89128099 89128099 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89128099 89128099 single base substitution C T missense_variant E1154K 3460G>A MELA-AU 14 89128099 89128099 single base substitution C T missense_variant E1192K 3574G>A MELA-AU 14 89128585 89128585 single base substitution C T intron_variant MELA-AU 14 89128985 89128985 single base substitution C T intron_variant MELA-AU 14 89129158 89129158 single base substitution G A intron_variant MELA-AU 14 89129403 89129403 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89129403 89129403 single base substitution C T missense_variant G1119E 3356G>A MELA-AU 14 89129403 89129403 single base substitution C T missense_variant G1157E 3470G>A MELA-AU 14 89129647 89129647 single base substitution C T intron_variant MELA-AU 14 89130105 89130105 single base substitution C T intron_variant MELA-AU 14 89131400 89131400 single base substitution G A intron_variant MELA-AU 14 89131423 89131423 single base substitution T A intron_variant MELA-AU 14 89131814 89131814 single base substitution A C 3_prime_UTR_variant MELA-AU 14 89131814 89131814 single base substitution A C missense_variant F1010L 3030T>G MELA-AU 14 89131814 89131814 single base substitution A C missense_variant F1048L 3144T>G MELA-AU 14 89131814 89131814 single base substitution A C upstream_gene_variant MELA-AU 14 89132035 89132035 single base substitution G A intron_variant MELA-AU 14 89132035 89132035 single base substitution G A upstream_gene_variant MELA-AU 14 89132065 89132065 single base substitution G A intron_variant MELA-AU 14 89132065 89132065 single base substitution G A upstream_gene_variant MELA-AU 14 89132147 89132147 single base substitution G A intron_variant MELA-AU 14 89132147 89132147 single base substitution G A upstream_gene_variant MELA-AU 14 89132166 89132166 single base substitution T A intron_variant MELA-AU 14 89132166 89132166 single base substitution T A upstream_gene_variant MELA-AU 14 89132415 89132415 single base substitution G A intron_variant MELA-AU 14 89132415 89132415 single base substitution G A upstream_gene_variant MELA-AU 14 89132920 89132920 single base substitution G A intron_variant MELA-AU 14 89132920 89132920 single base substitution G A upstream_gene_variant MELA-AU 14 89132964 89132964 single base substitution G A intron_variant MELA-AU 14 89132964 89132964 single base substitution G A upstream_gene_variant MELA-AU 14 89133138 89133138 single base substitution G A intron_variant MELA-AU 14 89133138 89133138 single base substitution G A upstream_gene_variant MELA-AU 14 89133151 89133151 single base substitution G A intron_variant MELA-AU 14 89133151 89133151 single base substitution G A upstream_gene_variant MELA-AU 14 89133329 89133330 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89133329 89133330 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 14 89133983 89133983 single base substitution G A intron_variant MELA-AU 14 89133983 89133983 single base substitution G A upstream_gene_variant MELA-AU 14 89134484 89134485 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89134484 89134485 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 14 89134718 89134718 single base substitution G A intron_variant MELA-AU 14 89134718 89134718 single base substitution G A upstream_gene_variant MELA-AU 14 89134876 89134876 single base substitution G A intron_variant MELA-AU 14 89134876 89134876 single base substitution G A upstream_gene_variant MELA-AU 14 89134888 89134888 single base substitution A T intron_variant MELA-AU 14 89134888 89134888 single base substitution A T upstream_gene_variant MELA-AU 14 89135181 89135181 single base substitution G A intron_variant MELA-AU 14 89135181 89135181 single base substitution G A upstream_gene_variant MELA-AU 14 89135222 89135222 single base substitution G A intron_variant MELA-AU 14 89135222 89135222 single base substitution G A upstream_gene_variant MELA-AU 14 89135529 89135529 single base substitution C T intron_variant MELA-AU 14 89135529 89135529 single base substitution C T upstream_gene_variant MELA-AU 14 89135533 89135533 single base substitution C T intron_variant MELA-AU 14 89135533 89135533 single base substitution C T upstream_gene_variant MELA-AU 14 89135756 89135756 single base substitution G A intron_variant MELA-AU 14 89135756 89135756 single base substitution G A upstream_gene_variant MELA-AU 14 89135956 89135956 single base substitution G A intron_variant MELA-AU 14 89135956 89135956 single base substitution G A upstream_gene_variant MELA-AU 14 89136124 89136124 single base substitution C T intron_variant MELA-AU 14 89136124 89136124 single base substitution C T upstream_gene_variant MELA-AU 14 89136152 89136152 single base substitution G A intron_variant MELA-AU 14 89136152 89136152 single base substitution G A upstream_gene_variant MELA-AU 14 89136187 89136187 single base substitution G A intron_variant MELA-AU 14 89136187 89136187 single base substitution G A upstream_gene_variant MELA-AU 14 89136279 89136279 single base substitution C T intron_variant MELA-AU 14 89136279 89136279 single base substitution C T upstream_gene_variant MELA-AU 14 89136305 89136305 single base substitution G A intron_variant MELA-AU 14 89136305 89136305 single base substitution G A upstream_gene_variant MELA-AU 14 89136548 89136549 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89136548 89136549 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 14 89136559 89136559 single base substitution G A intron_variant MELA-AU 14 89136559 89136559 single base substitution G A upstream_gene_variant MELA-AU 14 89137159 89137159 single base substitution T C intron_variant MELA-AU 14 89137222 89137222 single base substitution G A intron_variant MELA-AU 14 89137703 89137703 single base substitution G A intron_variant MELA-AU 14 89137727 89137727 single base substitution T A intron_variant MELA-AU 14 89137745 89137745 single base substitution G A intron_variant MELA-AU 14 89137764 89137764 single base substitution G A intron_variant MELA-AU 14 89137771 89137771 single base substitution G A intron_variant MELA-AU 14 89137806 89137806 single base substitution G A intron_variant MELA-AU 14 89138478 89138478 single base substitution C T intron_variant MELA-AU 14 89138623 89138623 single base substitution A G intron_variant MELA-AU 14 89138655 89138655 single base substitution G A intron_variant MELA-AU 14 89138753 89138753 single base substitution G A intron_variant MELA-AU 14 89138907 89138907 single base substitution G A intron_variant MELA-AU 14 89138965 89138965 single base substitution G A intron_variant MELA-AU 14 89139174 89139174 single base substitution G A intron_variant MELA-AU 14 89139357 89139357 single base substitution G A intron_variant MELA-AU 14 89139460 89139460 single base substitution G A intron_variant MELA-AU 14 89139534 89139534 single base substitution G A intron_variant MELA-AU 14 89139613 89139613 single base substitution G A intron_variant MELA-AU 14 89139720 89139720 single base substitution G A intron_variant MELA-AU 14 89139970 89139970 single base substitution A T intron_variant MELA-AU 14 89140090 89140090 single base substitution G A intron_variant MELA-AU 14 89140093 89140094 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89140233 89140233 single base substitution G A intron_variant MELA-AU 14 89140361 89140361 single base substitution C T intron_variant MELA-AU 14 89140540 89140540 single base substitution G A intron_variant MELA-AU 14 89140598 89140598 single base substitution G A intron_variant MELA-AU 14 89140668 89140668 single base substitution G A intron_variant MELA-AU 14 89140920 89140920 single base substitution G A intron_variant MELA-AU 14 89140991 89140991 single base substitution C T intron_variant MELA-AU 14 89141206 89141206 single base substitution G A intron_variant MELA-AU 14 89141309 89141309 single base substitution C T intron_variant MELA-AU 14 89141343 89141343 single base substitution C T intron_variant MELA-AU 14 89141540 89141540 single base substitution T C intron_variant MELA-AU 14 89141680 89141680 single base substitution C T intron_variant MELA-AU 14 89142080 89142080 single base substitution C T intron_variant MELA-AU 14 89142197 89142197 single base substitution C T intron_variant MELA-AU 14 89142251 89142251 single base substitution C A intron_variant MELA-AU 14 89142292 89142292 single base substitution C T intron_variant MELA-AU 14 89142448 89142448 single base substitution C T intron_variant MELA-AU 14 89142451 89142451 single base substitution A G intron_variant MELA-AU 14 89142579 89142579 single base substitution G A intron_variant MELA-AU 14 89142583 89142583 single base substitution A C intron_variant MELA-AU 14 89142693 89142693 single base substitution C T intron_variant MELA-AU 14 89142859 89142859 single base substitution G A intron_variant MELA-AU 14 89142873 89142873 single base substitution G A intron_variant MELA-AU 14 89143048 89143048 single base substitution G A intron_variant MELA-AU 14 89143110 89143110 single base substitution G A intron_variant MELA-AU 14 89143552 89143552 single base substitution T C intron_variant MELA-AU 14 89143555 89143555 single base substitution C T intron_variant MELA-AU 14 89143740 89143740 single base substitution A T intron_variant MELA-AU 14 89143756 89143756 single base substitution A T intron_variant MELA-AU 14 89143798 89143798 single base substitution G A intron_variant MELA-AU 14 89143937 89143937 single base substitution A G intron_variant MELA-AU 14 89143977 89143977 single base substitution A C intron_variant MELA-AU 14 89145385 89145385 single base substitution A C intron_variant MELA-AU 14 89145588 89145588 single base substitution T C intron_variant MELA-AU 14 89145889 89145889 single base substitution A G intron_variant MELA-AU 14 89146174 89146174 single base substitution G A intron_variant MELA-AU 14 89146253 89146253 single base substitution C A intron_variant MELA-AU 14 89146607 89146607 single base substitution C T intron_variant MELA-AU 14 89146816 89146816 single base substitution T A intron_variant MELA-AU 14 89147240 89147240 single base substitution G A intron_variant MELA-AU 14 89147397 89147397 single base substitution A C intron_variant MELA-AU 14 89147535 89147535 single base substitution G A intron_variant MELA-AU 14 89147562 89147562 single base substitution G A intron_variant MELA-AU 14 89147773 89147773 single base substitution G A intron_variant MELA-AU 14 89148196 89148196 single base substitution G A intron_variant MELA-AU 14 89148295 89148295 single base substitution G A 3_prime_UTR_variant MELA-AU 14 89148295 89148295 single base substitution G A synonymous_variant T1021T 3063C>T MELA-AU 14 89148295 89148295 single base substitution G A synonymous_variant T983T 2949C>T MELA-AU 14 89148571 89148571 single base substitution A G intron_variant MELA-AU 14 89148814 89148814 single base substitution G A intron_variant MELA-AU 14 89148962 89148962 single base substitution C T intron_variant MELA-AU 14 89149014 89149014 single base substitution C A intron_variant MELA-AU 14 89149301 89149301 single base substitution G A intron_variant MELA-AU 14 89149362 89149362 single base substitution C T intron_variant MELA-AU 14 89149431 89149431 single base substitution A G intron_variant MELA-AU 14 89149722 89149722 single base substitution G A intron_variant MELA-AU 14 89149999 89149999 single base substitution G A intron_variant MELA-AU 14 89150343 89150343 single base substitution G A intron_variant MELA-AU 14 89150932 89150932 single base substitution T A intron_variant MELA-AU 14 89151027 89151027 single base substitution C T intron_variant MELA-AU 14 89151255 89151256 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89151328 89151328 single base substitution G A intron_variant MELA-AU 14 89151339 89151339 single base substitution A T intron_variant MELA-AU 14 89151501 89151501 single base substitution G A intron_variant MELA-AU 14 89151584 89151584 single base substitution A G intron_variant MELA-AU 14 89151852 89151852 single base substitution C T intron_variant MELA-AU 14 89152053 89152053 single base substitution C T intron_variant MELA-AU 14 89152094 89152094 single base substitution C T intron_variant MELA-AU 14 89152415 89152415 single base substitution G A intron_variant MELA-AU 14 89152472 89152472 single base substitution G A intron_variant MELA-AU 14 89152487 89152487 single base substitution A G intron_variant MELA-AU 14 89152544 89152544 single base substitution G A intron_variant MELA-AU 14 89152610 89152610 single base substitution G A intron_variant MELA-AU 14 89152922 89152922 single base substitution G A intron_variant MELA-AU 14 89152948 89152948 single base substitution G A intron_variant MELA-AU 14 89153183 89153183 single base substitution G A intron_variant MELA-AU 14 89153461 89153461 single base substitution G A intron_variant MELA-AU 14 89153527 89153527 single base substitution C T intron_variant MELA-AU 14 89153703 89153703 single base substitution G A intron_variant MELA-AU 14 89153798 89153798 single base substitution G A intron_variant MELA-AU 14 89154407 89154408 multiple base substitution (>=2bp and <=200bp) AC TT intron_variant MELA-AU 14 89154759 89154759 single base substitution C T intron_variant MELA-AU 14 89154759 89154759 single base substitution C T missense_variant M866I 2598G>A MELA-AU 14 89154784 89154784 single base substitution C T intron_variant MELA-AU 14 89154784 89154784 single base substitution C T missense_variant G858D 2573G>A MELA-AU 14 89154929 89154929 single base substitution A G intron_variant MELA-AU 14 89155186 89155186 single base substitution G A intron_variant MELA-AU 14 89155210 89155210 single base substitution C A intron_variant MELA-AU 14 89155283 89155283 single base substitution G A intron_variant MELA-AU 14 89155689 89155689 single base substitution G A intron_variant MELA-AU 14 89155716 89155716 single base substitution C T intron_variant MELA-AU 14 89155768 89155768 single base substitution G A intron_variant MELA-AU 14 89156308 89156308 single base substitution T A intron_variant MELA-AU 14 89156419 89156419 single base substitution G A intron_variant MELA-AU 14 89156523 89156523 single base substitution G A intron_variant MELA-AU 14 89156938 89156938 single base substitution G A intron_variant MELA-AU 14 89156975 89156975 single base substitution G A intron_variant MELA-AU 14 89157622 89157622 single base substitution G A intron_variant MELA-AU 14 89157685 89157685 single base substitution C T intron_variant MELA-AU 14 89157962 89157962 single base substitution C T intron_variant MELA-AU 14 89158198 89158198 single base substitution C T intron_variant MELA-AU 14 89158316 89158316 single base substitution C G intron_variant MELA-AU 14 89158335 89158335 single base substitution C T intron_variant MELA-AU 14 89158448 89158448 single base substitution G A intron_variant MELA-AU 14 89158503 89158503 single base substitution G A intron_variant MELA-AU 14 89158603 89158603 deletion of <=200bp C - intron_variant MELA-AU 14 89158668 89158669 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89158735 89158735 single base substitution G A intron_variant MELA-AU 14 89158844 89158844 single base substitution C T intron_variant MELA-AU 14 89158877 89158877 single base substitution G A intron_variant MELA-AU 14 89158878 89158878 single base substitution G A intron_variant MELA-AU 14 89158922 89158922 single base substitution G A intron_variant MELA-AU 14 89158937 89158937 single base substitution G A intron_variant MELA-AU 14 89159019 89159019 single base substitution G A intron_variant MELA-AU 14 89159162 89159162 single base substitution C T intron_variant MELA-AU 14 89159424 89159424 single base substitution C A intron_variant MELA-AU 14 89159632 89159632 single base substitution G A intron_variant MELA-AU 14 89160010 89160010 single base substitution A G intron_variant MELA-AU 14 89160265 89160266 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89160518 89160518 single base substitution C T intron_variant MELA-AU 14 89160521 89160521 single base substitution C T intron_variant MELA-AU 14 89160544 89160544 single base substitution C T intron_variant MELA-AU 14 89160749 89160749 single base substitution C T missense_variant G814E 2441G>A MELA-AU 14 89160749 89160749 single base substitution C T splice_region_variant MELA-AU 14 89160848 89160848 single base substitution G A intron_variant MELA-AU 14 89160929 89160929 single base substitution C T intron_variant MELA-AU 14 89161102 89161102 single base substitution T C intron_variant MELA-AU 14 89161370 89161370 single base substitution T C intron_variant MELA-AU 14 89161459 89161459 single base substitution G A intron_variant MELA-AU 14 89161516 89161516 insertion of <=200bp - A intron_variant MELA-AU 14 89161704 89161704 single base substitution C T splice_donor_variant MELA-AU 14 89161791 89161791 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89161791 89161791 single base substitution C T synonymous_variant G784G 2352G>A MELA-AU 14 89162083 89162083 single base substitution G A intron_variant MELA-AU 14 89162955 89162955 single base substitution A C intron_variant MELA-AU 14 89163724 89163724 single base substitution C T intron_variant MELA-AU 14 89164279 89164279 single base substitution C T intron_variant MELA-AU 14 89164381 89164381 single base substitution G A intron_variant MELA-AU 14 89164663 89164663 single base substitution G A intron_variant MELA-AU 14 89164719 89164720 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 89164802 89164802 single base substitution G A intron_variant MELA-AU 14 89165152 89165152 single base substitution G A intron_variant MELA-AU 14 89165222 89165222 single base substitution G A intron_variant MELA-AU 14 89165290 89165290 single base substitution G A intron_variant MELA-AU 14 89165294 89165294 single base substitution G A intron_variant MELA-AU 14 89165311 89165311 single base substitution G A intron_variant MELA-AU 14 89165546 89165546 single base substitution G A intron_variant MELA-AU 14 89166026 89166026 single base substitution G C intron_variant MELA-AU 14 89166252 89166252 single base substitution C T intron_variant MELA-AU 14 89166668 89166668 single base substitution G A intron_variant MELA-AU 14 89166690 89166690 single base substitution G A intron_variant MELA-AU 14 89166772 89166772 single base substitution C T intron_variant MELA-AU 14 89166819 89166819 single base substitution G A intron_variant MELA-AU 14 89166843 89166843 single base substitution G A intron_variant MELA-AU 14 89166863 89166863 single base substitution A G intron_variant MELA-AU 14 89166958 89166958 single base substitution C T intron_variant MELA-AU 14 89167219 89167219 single base substitution G A intron_variant MELA-AU 14 89167298 89167299 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89167613 89167613 single base substitution C G intron_variant MELA-AU 14 89167947 89167947 single base substitution G A intron_variant MELA-AU 14 89168014 89168014 single base substitution C T intron_variant MELA-AU 14 89168136 89168136 single base substitution C T intron_variant MELA-AU 14 89168168 89168168 single base substitution G A intron_variant MELA-AU 14 89169129 89169129 single base substitution C T intron_variant MELA-AU 14 89169279 89169279 single base substitution C T intron_variant MELA-AU 14 89169446 89169446 single base substitution C G intron_variant MELA-AU 14 89169889 89169889 single base substitution C T intron_variant MELA-AU 14 89170140 89170140 single base substitution A T intron_variant MELA-AU 14 89170197 89170197 single base substitution G A intron_variant MELA-AU 14 89170449 89170449 single base substitution G A intron_variant MELA-AU 14 89170494 89170494 single base substitution C T intron_variant MELA-AU 14 89170601 89170601 single base substitution G A intron_variant MELA-AU 14 89170623 89170623 single base substitution C T intron_variant MELA-AU 14 89170782 89170782 single base substitution C T intron_variant MELA-AU 14 89171110 89171110 single base substitution T C intron_variant MELA-AU 14 89171369 89171369 single base substitution T A intron_variant MELA-AU 14 89171535 89171535 single base substitution C T intron_variant MELA-AU 14 89171575 89171575 single base substitution G A intron_variant MELA-AU 14 89171710 89171710 single base substitution T C intron_variant MELA-AU 14 89171765 89171766 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89171940 89171940 single base substitution T A splice_region_variant MELA-AU 14 89171950 89171950 single base substitution G A intron_variant MELA-AU 14 89171994 89171994 single base substitution G A intron_variant MELA-AU 14 89172021 89172021 single base substitution A T intron_variant MELA-AU 14 89172069 89172069 single base substitution C T 3_prime_UTR_variant MELA-AU 14 89172069 89172069 single base substitution C T intron_variant MELA-AU 14 89172731 89172731 single base substitution A C exon_variant MELA-AU 14 89172731 89172731 single base substitution A C missense_variant V566G 1697T>G MELA-AU 14 89172946 89172946 single base substitution T C intron_variant MELA-AU 14 89173593 89173593 single base substitution C T intron_variant MELA-AU 14 89173613 89173613 single base substitution A G intron_variant MELA-AU 14 89173620 89173620 single base substitution T C intron_variant MELA-AU 14 89173646 89173646 single base substitution A T intron_variant MELA-AU 14 89173692 89173692 single base substitution G A intron_variant MELA-AU 14 89173803 89173803 single base substitution C T intron_variant MELA-AU 14 89173853 89173853 single base substitution G A intron_variant MELA-AU 14 89173949 89173949 single base substitution G A intron_variant MELA-AU 14 89174906 89174906 single base substitution G A intron_variant MELA-AU 14 89175269 89175269 single base substitution G A intron_variant MELA-AU 14 89175317 89175317 single base substitution G A intron_variant MELA-AU 14 89175638 89175638 single base substitution T C intron_variant MELA-AU 14 89175807 89175807 single base substitution G A intron_variant MELA-AU 14 89176073 89176073 single base substitution C T intron_variant MELA-AU 14 89176097 89176097 single base substitution G A intron_variant MELA-AU 14 89176123 89176123 single base substitution G A intron_variant MELA-AU 14 89176213 89176213 single base substitution G A intron_variant MELA-AU 14 89176277 89176277 single base substitution G A intron_variant MELA-AU 14 89176297 89176297 single base substitution G A intron_variant MELA-AU 14 89176487 89176487 single base substitution T C intron_variant MELA-AU 14 89176969 89176969 single base substitution C T intron_variant MELA-AU 14 89177000 89177000 single base substitution T C intron_variant MELA-AU 14 89177656 89177656 single base substitution C T intron_variant MELA-AU 14 89177680 89177680 single base substitution G A intron_variant MELA-AU 14 89177705 89177705 single base substitution G A intron_variant MELA-AU 14 89177749 89177749 single base substitution G A intron_variant MELA-AU 14 89177771 89177771 single base substitution G A intron_variant MELA-AU 14 89177822 89177822 single base substitution C T intron_variant MELA-AU 14 89177836 89177836 single base substitution G A intron_variant MELA-AU 14 89177906 89177906 single base substitution G A intron_variant MELA-AU 14 89177955 89177955 single base substitution A C intron_variant MELA-AU 14 89178491 89178491 single base substitution A G intron_variant MELA-AU 14 89178525 89178525 single base substitution G A intron_variant MELA-AU 14 89178688 89178688 single base substitution A T exon_variant MELA-AU 14 89178688 89178688 single base substitution A T stop_gained Y528* 1584T>A MELA-AU 14 89178780 89178781 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 14 89178780 89178781 multiple base substitution (>=2bp and <=200bp) CC TT stop_gained WA497*T MELA-AU 14 89179078 89179078 single base substitution G A intron_variant MELA-AU 14 89179200 89179200 single base substitution G A intron_variant MELA-AU 14 89179483 89179483 single base substitution C T intron_variant MELA-AU 14 89179502 89179502 single base substitution G A intron_variant MELA-AU 14 89179599 89179599 single base substitution G A intron_variant MELA-AU 14 89179707 89179707 single base substitution A G intron_variant MELA-AU 14 89179786 89179786 single base substitution C T intron_variant MELA-AU 14 89179847 89179847 single base substitution G A intron_variant MELA-AU 14 89179885 89179885 single base substitution G A intron_variant MELA-AU 14 89180124 89180124 single base substitution G A intron_variant MELA-AU 14 89180307 89180307 single base substitution G A intron_variant MELA-AU 14 89180317 89180317 single base substitution G A intron_variant MELA-AU 14 89180748 89180748 single base substitution G A intron_variant MELA-AU 14 89180956 89180957 multiple base substitution (>=2bp and <=200bp) GG GA intron_variant MELA-AU 14 89181097 89181097 single base substitution T C intron_variant MELA-AU 14 89181190 89181190 single base substitution C T intron_variant MELA-AU 14 89181227 89181227 single base substitution A G intron_variant MELA-AU 14 89181378 89181378 single base substitution G A exon_variant MELA-AU 14 89181378 89181378 single base substitution G A missense_variant S450F 1349C>T MELA-AU 14 89181826 89181826 single base substitution G A intron_variant MELA-AU 14 89181826 89181826 single base substitution G A upstream_gene_variant MELA-AU 14 89182138 89182138 single base substitution C T intron_variant MELA-AU 14 89182138 89182138 single base substitution C T upstream_gene_variant MELA-AU 14 89182383 89182383 single base substitution G A intron_variant MELA-AU 14 89182383 89182383 single base substitution G A upstream_gene_variant MELA-AU 14 89182416 89182416 single base substitution C T intron_variant MELA-AU 14 89182416 89182416 single base substitution C T upstream_gene_variant MELA-AU 14 89182708 89182708 single base substitution C T intron_variant MELA-AU 14 89182708 89182708 single base substitution C T upstream_gene_variant MELA-AU 14 89182834 89182834 single base substitution G A intron_variant MELA-AU 14 89182834 89182834 single base substitution G A upstream_gene_variant MELA-AU 14 89182835 89182835 single base substitution G T intron_variant MELA-AU 14 89182835 89182835 single base substitution G T upstream_gene_variant MELA-AU 14 89183165 89183165 single base substitution C T intron_variant MELA-AU 14 89183165 89183165 single base substitution C T upstream_gene_variant MELA-AU 14 89183254 89183254 single base substitution G A intron_variant MELA-AU 14 89183254 89183254 single base substitution G A upstream_gene_variant MELA-AU 14 89183400 89183400 single base substitution G A intron_variant MELA-AU 14 89183400 89183400 single base substitution G A upstream_gene_variant MELA-AU 14 89183426 89183426 single base substitution C T intron_variant MELA-AU 14 89183426 89183426 single base substitution C T upstream_gene_variant MELA-AU 14 89183461 89183461 single base substitution G A intron_variant MELA-AU 14 89183461 89183461 single base substitution G A upstream_gene_variant MELA-AU 14 89183515 89183515 single base substitution G A intron_variant MELA-AU 14 89183515 89183515 single base substitution G A upstream_gene_variant MELA-AU 14 89183562 89183562 single base substitution G A intron_variant MELA-AU 14 89183562 89183562 single base substitution G A upstream_gene_variant MELA-AU 14 89183665 89183666 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89183665 89183666 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 14 89183696 89183696 single base substitution G A intron_variant MELA-AU 14 89183696 89183696 single base substitution G A upstream_gene_variant MELA-AU 14 89183820 89183820 single base substitution A T intron_variant MELA-AU 14 89183820 89183820 single base substitution A T upstream_gene_variant MELA-AU 14 89184007 89184007 single base substitution G A intron_variant MELA-AU 14 89184007 89184007 single base substitution G A upstream_gene_variant MELA-AU 14 89184026 89184026 single base substitution G A intron_variant MELA-AU 14 89184026 89184026 single base substitution G A upstream_gene_variant MELA-AU 14 89184283 89184283 single base substitution G A intron_variant MELA-AU 14 89184283 89184283 single base substitution G A upstream_gene_variant MELA-AU 14 89184355 89184355 single base substitution A T intron_variant MELA-AU 14 89184355 89184355 single base substitution A T upstream_gene_variant MELA-AU 14 89184506 89184506 single base substitution G A intron_variant MELA-AU 14 89184506 89184506 single base substitution G A upstream_gene_variant MELA-AU 14 89184598 89184598 single base substitution G A intron_variant MELA-AU 14 89184598 89184598 single base substitution G A upstream_gene_variant MELA-AU 14 89184614 89184614 single base substitution G A intron_variant MELA-AU 14 89184614 89184614 single base substitution G A upstream_gene_variant MELA-AU 14 89184713 89184713 single base substitution G A intron_variant MELA-AU 14 89184713 89184713 single base substitution G A upstream_gene_variant MELA-AU 14 89184791 89184791 single base substitution G A intron_variant MELA-AU 14 89184791 89184791 single base substitution G A upstream_gene_variant MELA-AU 14 89184811 89184811 single base substitution A T intron_variant MELA-AU 14 89184811 89184811 single base substitution A T upstream_gene_variant MELA-AU 14 89184982 89184982 single base substitution G A intron_variant MELA-AU 14 89184982 89184982 single base substitution G A upstream_gene_variant MELA-AU 14 89185001 89185001 single base substitution G A intron_variant MELA-AU 14 89185001 89185001 single base substitution G A upstream_gene_variant MELA-AU 14 89185113 89185113 single base substitution G A intron_variant MELA-AU 14 89185113 89185113 single base substitution G A upstream_gene_variant MELA-AU 14 89185195 89185195 single base substitution C T intron_variant MELA-AU 14 89185195 89185195 single base substitution C T upstream_gene_variant MELA-AU 14 89185263 89185263 single base substitution G A intron_variant MELA-AU 14 89185263 89185263 single base substitution G A upstream_gene_variant MELA-AU 14 89185291 89185291 single base substitution G A intron_variant MELA-AU 14 89185291 89185291 single base substitution G A upstream_gene_variant MELA-AU 14 89185465 89185465 single base substitution C T intron_variant MELA-AU 14 89185465 89185465 single base substitution C T upstream_gene_variant MELA-AU 14 89185656 89185656 single base substitution G A intron_variant MELA-AU 14 89185656 89185656 single base substitution G A upstream_gene_variant MELA-AU 14 89185891 89185891 single base substitution G A intron_variant MELA-AU 14 89185891 89185891 single base substitution G A upstream_gene_variant MELA-AU 14 89186074 89186074 single base substitution G A intron_variant MELA-AU 14 89186074 89186074 single base substitution G A upstream_gene_variant MELA-AU 14 89186256 89186256 single base substitution G A intron_variant MELA-AU 14 89186256 89186256 single base substitution G A upstream_gene_variant MELA-AU 14 89186295 89186295 single base substitution G A intron_variant MELA-AU 14 89186295 89186295 single base substitution G A upstream_gene_variant MELA-AU 14 89186447 89186447 single base substitution C T intron_variant MELA-AU 14 89186447 89186447 single base substitution C T upstream_gene_variant MELA-AU 14 89187121 89187121 single base substitution G A intron_variant MELA-AU 14 89187271 89187271 single base substitution G A intron_variant MELA-AU 14 89187278 89187278 single base substitution G A intron_variant MELA-AU 14 89188065 89188065 single base substitution G A intron_variant MELA-AU 14 89188132 89188132 single base substitution G A intron_variant MELA-AU 14 89188715 89188715 single base substitution C T intron_variant MELA-AU 14 89188809 89188809 single base substitution G A intron_variant MELA-AU 14 89188903 89188903 single base substitution A T intron_variant MELA-AU 14 89189035 89189035 single base substitution C T intron_variant MELA-AU 14 89189353 89189353 single base substitution G A intron_variant MELA-AU 14 89189362 89189362 single base substitution G A intron_variant MELA-AU 14 89189495 89189495 single base substitution G A intron_variant MELA-AU 14 89189632 89189632 single base substitution C T intron_variant MELA-AU 14 89189778 89189778 single base substitution C T intron_variant MELA-AU 14 89190381 89190381 single base substitution G A intron_variant MELA-AU 14 89190432 89190432 single base substitution G A intron_variant MELA-AU 14 89190629 89190629 single base substitution A T intron_variant MELA-AU 14 89191057 89191057 single base substitution G A intron_variant MELA-AU 14 89191292 89191292 single base substitution C T intron_variant MELA-AU 14 89191421 89191421 single base substitution G A intron_variant MELA-AU 14 89191692 89191692 deletion of <=200bp A - intron_variant MELA-AU 14 89191771 89191771 single base substitution G A intron_variant MELA-AU 14 89192110 89192110 single base substitution A C intron_variant MELA-AU 14 89192180 89192180 single base substitution G A intron_variant MELA-AU 14 89192332 89192332 single base substitution C T intron_variant MELA-AU 14 89192391 89192391 single base substitution C T intron_variant MELA-AU 14 89192553 89192553 single base substitution G A intron_variant MELA-AU 14 89192762 89192762 single base substitution G A intron_variant MELA-AU 14 89193200 89193200 single base substitution T C intron_variant MELA-AU 14 89193306 89193306 single base substitution G A intron_variant MELA-AU 14 89193320 89193320 single base substitution C T intron_variant MELA-AU 14 89193780 89193780 single base substitution C T intron_variant MELA-AU 14 89193794 89193794 single base substitution G A intron_variant MELA-AU 14 89193855 89193855 single base substitution C T intron_variant MELA-AU 14 89194118 89194118 single base substitution G A intron_variant MELA-AU 14 89194198 89194198 single base substitution G A intron_variant MELA-AU 14 89194493 89194493 single base substitution G A intron_variant MELA-AU 14 89194555 89194555 single base substitution T G intron_variant MELA-AU 14 89194565 89194565 single base substitution C T intron_variant MELA-AU 14 89194666 89194678 deletion of <=200bp GCACCAGTTAGAA - intron_variant MELA-AU 14 89194871 89194871 single base substitution C T intron_variant MELA-AU 14 89194877 89194877 single base substitution G A intron_variant MELA-AU 14 89195327 89195327 single base substitution G A intron_variant MELA-AU 14 89195335 89195335 single base substitution G A intron_variant MELA-AU 14 89195809 89195809 single base substitution A T intron_variant MELA-AU 14 89195908 89195909 deletion of <=200bp TG - intron_variant MELA-AU 14 89196038 89196038 single base substitution G A intron_variant MELA-AU 14 89196039 89196039 single base substitution G A intron_variant MELA-AU 14 89196218 89196218 single base substitution T G intron_variant MELA-AU 14 89196381 89196381 single base substitution G A intron_variant MELA-AU 14 89196437 89196437 single base substitution T C intron_variant MELA-AU 14 89196459 89196459 single base substitution G A intron_variant MELA-AU 14 89196695 89196695 single base substitution A G intron_variant MELA-AU 14 89196811 89196811 single base substitution G A intron_variant MELA-AU 14 89197552 89197552 single base substitution A G intron_variant MELA-AU 14 89197971 89197971 single base substitution C T intron_variant MELA-AU 14 89198066 89198066 single base substitution C T intron_variant MELA-AU 14 89199181 89199181 single base substitution G A intron_variant MELA-AU 14 89199637 89199637 single base substitution G A intron_variant MELA-AU 14 89199709 89199709 single base substitution C T intron_variant MELA-AU 14 89199943 89199943 single base substitution C T intron_variant MELA-AU 14 89200078 89200078 single base substitution A C intron_variant MELA-AU 14 89200554 89200554 single base substitution T G intron_variant MELA-AU 14 89200933 89200933 single base substitution T C intron_variant MELA-AU 14 89200989 89200989 single base substitution G A intron_variant MELA-AU 14 89200999 89200999 single base substitution T C intron_variant MELA-AU 14 89201199 89201199 single base substitution G A intron_variant MELA-AU 14 89201278 89201278 single base substitution G A intron_variant MELA-AU 14 89201414 89201414 single base substitution G A intron_variant MELA-AU 14 89201894 89201894 single base substitution G A intron_variant MELA-AU 14 89201932 89201932 single base substitution G A intron_variant MELA-AU 14 89202189 89202189 single base substitution G A intron_variant MELA-AU 14 89202394 89202394 single base substitution G A intron_variant MELA-AU 14 89202758 89202758 single base substitution G A synonymous_variant V333V 999C>T MELA-AU 14 89202810 89202810 single base substitution G A missense_variant P316L 947C>T MELA-AU 14 89202838 89202838 single base substitution C T missense_variant E307K 919G>A MELA-AU 14 89203861 89203861 single base substitution G A intron_variant MELA-AU 14 89203940 89203940 single base substitution A G intron_variant MELA-AU 14 89203942 89203942 single base substitution A T intron_variant MELA-AU 14 89204051 89204051 single base substitution G A intron_variant MELA-AU 14 89204074 89204074 single base substitution C T intron_variant MELA-AU 14 89204255 89204255 single base substitution T A intron_variant MELA-AU 14 89204499 89204499 single base substitution G A intron_variant MELA-AU 14 89204976 89204976 single base substitution C T intron_variant MELA-AU 14 89205765 89205765 single base substitution C A intron_variant MELA-AU 14 89206117 89206117 single base substitution G A intron_variant MELA-AU 14 89206210 89206210 single base substitution A C intron_variant MELA-AU 14 89206372 89206372 single base substitution G A intron_variant MELA-AU 14 89206768 89206768 single base substitution C T missense_variant G225E 674G>A MELA-AU 14 89206806 89206806 single base substitution A T stop_gained Y212* 636T>A MELA-AU 14 89206923 89206923 single base substitution G A splice_region_variant MELA-AU 14 89206980 89206980 single base substitution C G intron_variant MELA-AU 14 89207640 89207640 single base substitution G A intron_variant MELA-AU 14 89207870 89207870 single base substitution G A intron_variant MELA-AU 14 89207901 89207901 single base substitution G A intron_variant MELA-AU 14 89207902 89207902 single base substitution G A intron_variant MELA-AU 14 89208067 89208067 single base substitution A G intron_variant MELA-AU 14 89208140 89208140 single base substitution G A intron_variant MELA-AU 14 89208435 89208435 single base substitution A T intron_variant MELA-AU 14 89208447 89208447 single base substitution G A intron_variant MELA-AU 14 89209445 89209445 single base substitution A G intron_variant MELA-AU 14 89209503 89209503 single base substitution G A intron_variant MELA-AU 14 89209653 89209653 single base substitution G A intron_variant MELA-AU 14 89210481 89210481 single base substitution C T intron_variant MELA-AU 14 89211031 89211031 single base substitution A G intron_variant MELA-AU 14 89211511 89211511 single base substitution T G intron_variant MELA-AU 14 89211975 89211975 single base substitution G A intron_variant MELA-AU 14 89212442 89212442 single base substitution C T intron_variant MELA-AU 14 89212956 89212956 single base substitution G A intron_variant MELA-AU 14 89213052 89213052 single base substitution G A intron_variant MELA-AU 14 89213108 89213108 single base substitution G A intron_variant MELA-AU 14 89213126 89213126 single base substitution G A intron_variant MELA-AU 14 89213299 89213299 single base substitution G A intron_variant MELA-AU 14 89214350 89214350 single base substitution T A intron_variant MELA-AU 14 89214756 89214756 single base substitution T C intron_variant MELA-AU 14 89214905 89214905 single base substitution T A intron_variant MELA-AU 14 89215021 89215021 single base substitution G A intron_variant MELA-AU 14 89215043 89215043 single base substitution A C intron_variant MELA-AU 14 89215110 89215110 single base substitution A C intron_variant MELA-AU 14 89215921 89215921 single base substitution G A intron_variant MELA-AU 14 89217846 89217846 single base substitution G A intron_variant MELA-AU 14 89218068 89218068 single base substitution G A intron_variant MELA-AU 14 89218964 89218964 single base substitution G A intron_variant MELA-AU 14 89219065 89219065 single base substitution G A intron_variant MELA-AU 14 89219282 89219282 single base substitution C T intron_variant MELA-AU 14 89219361 89219361 single base substitution C T intron_variant MELA-AU 14 89219393 89219393 single base substitution G A intron_variant MELA-AU 14 89219615 89219615 single base substitution G A intron_variant MELA-AU 14 89219623 89219623 single base substitution C T intron_variant MELA-AU 14 89219706 89219706 single base substitution G A intron_variant MELA-AU 14 89219761 89219761 single base substitution G A intron_variant MELA-AU 14 89219862 89219862 single base substitution G A intron_variant MELA-AU 14 89220030 89220030 single base substitution G A intron_variant MELA-AU 14 89220124 89220124 single base substitution G A intron_variant MELA-AU 14 89220364 89220364 single base substitution C T intron_variant MELA-AU 14 89220686 89220686 single base substitution G A intron_variant MELA-AU 14 89220787 89220787 single base substitution G A intron_variant MELA-AU 14 89221182 89221182 single base substitution C T intron_variant MELA-AU 14 89221284 89221284 single base substitution G A intron_variant MELA-AU 14 89221306 89221306 single base substitution G A intron_variant MELA-AU 14 89221696 89221696 single base substitution C T intron_variant MELA-AU 14 89221822 89221822 single base substitution C T intron_variant MELA-AU 14 89221905 89221906 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89222009 89222009 single base substitution G A intron_variant MELA-AU 14 89222023 89222023 single base substitution G A intron_variant MELA-AU 14 89222168 89222168 single base substitution C T intron_variant MELA-AU 14 89222337 89222337 single base substitution G A intron_variant MELA-AU 14 89222409 89222410 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 89222526 89222526 single base substitution G A intron_variant MELA-AU 14 89222552 89222552 single base substitution G A intron_variant MELA-AU 14 89222568 89222568 single base substitution G A intron_variant MELA-AU 14 89222614 89222614 single base substitution C T intron_variant MELA-AU 14 89222627 89222627 single base substitution G A intron_variant MELA-AU 14 89222666 89222666 single base substitution A T intron_variant MELA-AU 14 89222712 89222712 single base substitution G A intron_variant MELA-AU 14 89222783 89222783 single base substitution G A intron_variant MELA-AU 14 89222852 89222852 single base substitution G A intron_variant MELA-AU 14 89222863 89222863 single base substitution G A intron_variant MELA-AU 14 89222965 89222965 single base substitution A G intron_variant MELA-AU 14 89222968 89222968 single base substitution A T intron_variant MELA-AU 14 89222979 89222979 single base substitution A G intron_variant MELA-AU 14 89222996 89222996 single base substitution G A intron_variant MELA-AU 14 89223126 89223126 single base substitution G A intron_variant MELA-AU 14 89223320 89223320 single base substitution G A intron_variant MELA-AU 14 89223680 89223680 single base substitution G A intron_variant MELA-AU 14 89223934 89223934 single base substitution A G intron_variant MELA-AU 14 89224080 89224080 single base substitution G A intron_variant MELA-AU 14 89224244 89224244 single base substitution G A intron_variant MELA-AU 14 89224809 89224809 single base substitution G A intron_variant MELA-AU 14 89224932 89224932 single base substitution G A intron_variant MELA-AU 14 89225006 89225006 single base substitution C T intron_variant MELA-AU 14 89225028 89225028 single base substitution A T intron_variant MELA-AU 14 89225031 89225031 single base substitution G A intron_variant MELA-AU 14 89225237 89225237 single base substitution G A intron_variant MELA-AU 14 89225457 89225457 single base substitution G A intron_variant MELA-AU 14 89225600 89225600 single base substitution G A intron_variant MELA-AU 14 89225722 89225722 single base substitution C T intron_variant MELA-AU 14 89225904 89225904 single base substitution C T intron_variant MELA-AU 14 89225910 89225910 single base substitution C T intron_variant MELA-AU 14 89226013 89226013 single base substitution G A intron_variant MELA-AU 14 89227298 89227298 single base substitution T C intron_variant MELA-AU 14 89227536 89227536 single base substitution G A intron_variant MELA-AU 14 89227707 89227707 single base substitution C T intron_variant MELA-AU 14 89228246 89228246 single base substitution G A intron_variant MELA-AU 14 89228653 89228653 single base substitution G A intron_variant MELA-AU 14 89228748 89228748 single base substitution G A intron_variant MELA-AU 14 89228749 89228749 single base substitution G A intron_variant MELA-AU 14 89228849 89228849 single base substitution C T intron_variant MELA-AU 14 89228859 89228859 single base substitution G A intron_variant MELA-AU 14 89228911 89228911 single base substitution G A intron_variant MELA-AU 14 89229031 89229031 single base substitution C T intron_variant MELA-AU 14 89229132 89229132 single base substitution G A intron_variant MELA-AU 14 89229401 89229401 single base substitution G A intron_variant MELA-AU 14 89229524 89229524 single base substitution G A intron_variant MELA-AU 14 89229625 89229625 single base substitution G A intron_variant MELA-AU 14 89229798 89229798 single base substitution G A intron_variant MELA-AU 14 89229808 89229808 single base substitution G A intron_variant MELA-AU 14 89229894 89229894 single base substitution G A intron_variant MELA-AU 14 89230037 89230037 single base substitution G A intron_variant MELA-AU 14 89230053 89230053 single base substitution G A intron_variant MELA-AU 14 89230084 89230084 single base substitution C T intron_variant MELA-AU 14 89230420 89230420 single base substitution C T intron_variant MELA-AU 14 89230456 89230456 single base substitution G A intron_variant MELA-AU 14 89230476 89230476 single base substitution G A intron_variant MELA-AU 14 89230534 89230534 single base substitution G A intron_variant MELA-AU 14 89230552 89230552 single base substitution C T intron_variant MELA-AU 14 89230670 89230670 single base substitution A C intron_variant MELA-AU 14 89230709 89230709 single base substitution G A intron_variant MELA-AU 14 89231030 89231030 single base substitution C T intron_variant MELA-AU 14 89231141 89231141 single base substitution C T intron_variant MELA-AU 14 89231224 89231224 single base substitution G A intron_variant MELA-AU 14 89231379 89231379 single base substitution G A intron_variant MELA-AU 14 89231635 89231635 single base substitution G A intron_variant MELA-AU 14 89231638 89231638 single base substitution G A intron_variant MELA-AU 14 89231715 89231715 single base substitution C T intron_variant MELA-AU 14 89231958 89231958 single base substitution C T intron_variant MELA-AU 14 89232076 89232076 single base substitution G A intron_variant MELA-AU 14 89232317 89232317 single base substitution A T intron_variant MELA-AU 14 89232422 89232422 single base substitution C T intron_variant MELA-AU 14 89232551 89232551 single base substitution C T intron_variant MELA-AU 14 89232585 89232585 single base substitution G A intron_variant MELA-AU 14 89232594 89232594 single base substitution G A intron_variant MELA-AU 14 89232717 89232717 single base substitution A T intron_variant MELA-AU 14 89232786 89232786 single base substitution G A intron_variant MELA-AU 14 89232845 89232845 single base substitution G A intron_variant MELA-AU 14 89232917 89232917 single base substitution G A intron_variant MELA-AU 14 89232956 89232956 single base substitution C T intron_variant MELA-AU 14 89233110 89233110 single base substitution G A intron_variant MELA-AU 14 89233502 89233502 single base substitution C T intron_variant MELA-AU 14 89234229 89234229 single base substitution A T intron_variant MELA-AU 14 89234531 89234531 single base substitution G A intron_variant MELA-AU 14 89234702 89234702 single base substitution A G intron_variant MELA-AU 14 89234858 89234858 single base substitution G A intron_variant MELA-AU 14 89234889 89234889 single base substitution G A intron_variant MELA-AU 14 89234955 89234955 single base substitution C T intron_variant MELA-AU 14 89234966 89234966 single base substitution G A intron_variant MELA-AU 14 89234975 89234975 single base substitution C T intron_variant MELA-AU 14 89235531 89235531 single base substitution C T intron_variant MELA-AU 14 89235644 89235644 single base substitution G A intron_variant MELA-AU 14 89235897 89235897 single base substitution C T intron_variant MELA-AU 14 89236109 89236109 single base substitution C T intron_variant MELA-AU 14 89236135 89236135 single base substitution G A intron_variant MELA-AU 14 89236139 89236139 single base substitution C T intron_variant MELA-AU 14 89236419 89236419 single base substitution G A intron_variant MELA-AU 14 89236544 89236544 single base substitution G A intron_variant MELA-AU 14 89236657 89236657 single base substitution C T intron_variant MELA-AU 14 89236757 89236757 single base substitution C T intron_variant MELA-AU 14 89236874 89236874 single base substitution G A intron_variant MELA-AU 14 89236908 89236908 single base substitution G A intron_variant MELA-AU 14 89237116 89237116 single base substitution G A intron_variant MELA-AU 14 89237221 89237221 single base substitution G A intron_variant MELA-AU 14 89237378 89237378 single base substitution G A intron_variant MELA-AU 14 89237419 89237419 single base substitution C T intron_variant MELA-AU 14 89237532 89237532 single base substitution G A intron_variant MELA-AU 14 89237647 89237647 single base substitution G A intron_variant MELA-AU 14 89237706 89237706 single base substitution C T intron_variant MELA-AU 14 89237938 89237938 single base substitution A G intron_variant MELA-AU 14 89238767 89238767 single base substitution G A intron_variant MELA-AU 14 89238881 89238881 single base substitution G A intron_variant MELA-AU 14 89238946 89238946 single base substitution A T intron_variant MELA-AU 14 89239238 89239238 single base substitution G A intron_variant MELA-AU 14 89239276 89239276 single base substitution C T intron_variant MELA-AU 14 89239726 89239726 single base substitution G A intron_variant MELA-AU 14 89239951 89239951 single base substitution C A intron_variant MELA-AU 14 89239984 89239984 single base substitution G A intron_variant MELA-AU 14 89240001 89240001 single base substitution C T intron_variant MELA-AU 14 89240243 89240243 single base substitution A T intron_variant MELA-AU 14 89240589 89240589 single base substitution A G intron_variant MELA-AU 14 89240645 89240645 single base substitution C T intron_variant MELA-AU 14 89241059 89241059 single base substitution G A intron_variant MELA-AU 14 89241060 89241060 single base substitution G A intron_variant MELA-AU 14 89241358 89241358 single base substitution G A intron_variant MELA-AU 14 89241480 89241480 single base substitution T A intron_variant MELA-AU 14 89241735 89241735 single base substitution G A intron_variant MELA-AU 14 89242004 89242004 single base substitution C T intron_variant MELA-AU 14 89242045 89242045 single base substitution G A intron_variant MELA-AU 14 89242297 89242297 single base substitution A G intron_variant MELA-AU 14 89242339 89242339 single base substitution C T intron_variant MELA-AU 14 89242599 89242599 single base substitution C A intron_variant MELA-AU 14 89242603 89242603 single base substitution G A intron_variant MELA-AU 14 89242791 89242791 single base substitution C T intron_variant MELA-AU 14 89242839 89242839 single base substitution C T intron_variant MELA-AU 14 89243208 89243208 single base substitution G A intron_variant MELA-AU 14 89243284 89243284 single base substitution A T intron_variant MELA-AU 14 89243381 89243381 single base substitution A T intron_variant MELA-AU 14 89243492 89243492 single base substitution G A intron_variant MELA-AU 14 89243517 89243517 single base substitution A G intron_variant MELA-AU 14 89243700 89243700 single base substitution G A intron_variant MELA-AU 14 89244003 89244003 single base substitution G A intron_variant MELA-AU 14 89244567 89244567 single base substitution G A intron_variant MELA-AU 14 89244582 89244582 single base substitution G A intron_variant MELA-AU 14 89244915 89244915 single base substitution G A intron_variant MELA-AU 14 89245470 89245470 single base substitution G T intron_variant MELA-AU 14 89245494 89245494 single base substitution G A intron_variant MELA-AU 14 89245797 89245797 single base substitution G C intron_variant MELA-AU 14 89246084 89246084 single base substitution G A intron_variant MELA-AU 14 89246144 89246144 single base substitution A G intron_variant MELA-AU 14 89246317 89246317 single base substitution G A intron_variant MELA-AU 14 89246328 89246328 single base substitution C T intron_variant MELA-AU 14 89246800 89246800 single base substitution G A intron_variant MELA-AU 14 89246983 89246983 single base substitution G A intron_variant MELA-AU 14 89247054 89247054 single base substitution G A intron_variant MELA-AU 14 89247055 89247055 single base substitution G A intron_variant MELA-AU 14 89247405 89247405 single base substitution G A intron_variant MELA-AU 14 89247429 89247429 single base substitution T C intron_variant MELA-AU 14 89247702 89247702 single base substitution G A intron_variant MELA-AU 14 89247739 89247739 single base substitution G A intron_variant MELA-AU 14 89247992 89247992 single base substitution G A intron_variant MELA-AU 14 89248041 89248041 single base substitution G A intron_variant MELA-AU 14 89248069 89248069 single base substitution C T intron_variant MELA-AU 14 89248285 89248285 single base substitution G A intron_variant MELA-AU 14 89248602 89248602 single base substitution G A intron_variant MELA-AU 14 89248646 89248646 single base substitution G A intron_variant MELA-AU 14 89248748 89248748 single base substitution G A intron_variant MELA-AU 14 89248810 89248810 single base substitution G A intron_variant MELA-AU 14 89249101 89249101 single base substitution G A intron_variant MELA-AU 14 89249152 89249152 single base substitution G A intron_variant MELA-AU 14 89249216 89249216 single base substitution G A intron_variant MELA-AU 14 89249356 89249356 single base substitution G A intron_variant MELA-AU 14 89249497 89249497 single base substitution G A intron_variant MELA-AU 14 89249519 89249519 single base substitution C T intron_variant MELA-AU 14 89249529 89249529 single base substitution G A intron_variant MELA-AU 14 89249542 89249542 single base substitution G A intron_variant MELA-AU 14 89249558 89249558 single base substitution G A intron_variant MELA-AU 14 89249689 89249689 single base substitution G A intron_variant MELA-AU 14 89250099 89250099 single base substitution C T intron_variant MELA-AU 14 89250295 89250295 single base substitution A T intron_variant MELA-AU 14 89250351 89250351 single base substitution G A intron_variant MELA-AU 14 89250402 89250402 single base substitution C T intron_variant MELA-AU 14 89250709 89250709 single base substitution T A intron_variant MELA-AU 14 89251444 89251444 single base substitution C T intron_variant MELA-AU 14 89251544 89251544 single base substitution G T intron_variant MELA-AU 14 89251878 89251878 single base substitution A G intron_variant MELA-AU 14 89252032 89252032 single base substitution C T intron_variant MELA-AU 14 89252112 89252112 single base substitution C A intron_variant MELA-AU 14 89252153 89252153 single base substitution C T intron_variant MELA-AU 14 89252705 89252705 single base substitution G A intron_variant MELA-AU 14 89252930 89252930 single base substitution G A intron_variant MELA-AU 14 89252962 89252962 single base substitution G A intron_variant MELA-AU 14 89253033 89253033 single base substitution C T intron_variant MELA-AU 14 89253050 89253050 single base substitution T G intron_variant MELA-AU 14 89253847 89253847 single base substitution G A intron_variant MELA-AU 14 89254483 89254483 single base substitution C T intron_variant MELA-AU 14 89255045 89255045 single base substitution C T intron_variant MELA-AU 14 89255046 89255046 single base substitution C T intron_variant MELA-AU 14 89255310 89255310 single base substitution G A intron_variant MELA-AU 14 89255806 89255806 single base substitution G A intron_variant MELA-AU 14 89259605 89259605 single base substitution C T upstream_gene_variant MELA-AU 14 89259992 89259992 single base substitution C A upstream_gene_variant MELA-AU 14 89260270 89260270 single base substitution C T upstream_gene_variant MELA-AU 14 89260467 89260467 single base substitution G A upstream_gene_variant MELA-AU 14 89260624 89260624 single base substitution A C upstream_gene_variant MELA-AU 14 89260627 89260627 single base substitution G A upstream_gene_variant MELA-AU 14 89260967 89260967 single base substitution G A upstream_gene_variant MELA-AU 14 89261094 89261094 single base substitution G A upstream_gene_variant MELA-AU 14 89261210 89261210 single base substitution C T upstream_gene_variant MELA-AU 14 89261297 89261297 single base substitution G A upstream_gene_variant MELA-AU 14 89261351 89261351 single base substitution G A upstream_gene_variant MELA-AU 14 89261503 89261503 single base substitution G A upstream_gene_variant MELA-AU 14 89261539 89261539 single base substitution G A upstream_gene_variant MELA-AU 14 89261989 89261989 single base substitution G A upstream_gene_variant MELA-AU 14 89262006 89262006 single base substitution C T upstream_gene_variant MELA-AU 14 89263797 89263797 single base substitution C T upstream_gene_variant MELA-AU 14 89263861 89263861 single base substitution T C upstream_gene_variant MELA-AU 14 89263950 89263950 single base substitution A G upstream_gene_variant MELA-AU 14 89263959 89263959 single base substitution G A upstream_gene_variant ORCA-IN 14 89083062 89083062 single base substitution A G downstream_gene_variant ORCA-IN 14 89083062 89083062 single base substitution A G splice_region_variant ORCA-IN 14 89094091 89094091 single base substitution G C 3_prime_UTR_variant ORCA-IN 14 89094091 89094091 single base substitution G C downstream_gene_variant ORCA-IN 14 89094091 89094091 single base substitution G C stop_gained S1431* 4292C>G ORCA-IN 14 89094091 89094091 single base substitution G C stop_gained S1469* 4406C>G ORCA-IN 14 89094091 89094091 single base substitution G C stop_gained S1477* 4430C>G ORCA-IN 14 89094091 89094091 single base substitution G C upstream_gene_variant ORCA-IN 14 89104774 89104774 single base substitution C T intron_variant ORCA-IN 14 89125797 89125797 single base substitution C G intron_variant ORCA-IN 14 89126145 89126145 single base substitution C T intron_variant ORCA-IN 14 89153898 89153898 single base substitution G A intron_variant ORCA-IN 14 89160701 89160701 single base substitution T A 3_prime_UTR_variant ORCA-IN 14 89160701 89160701 single base substitution T A missense_variant D830V 2489A>T ORCA-IN 14 89160750 89160750 single base substitution C T missense_variant G814R 2440G>A ORCA-IN 14 89160750 89160750 single base substitution C T splice_region_variant ORCA-IN 14 89173614 89173614 single base substitution T A intron_variant ORCA-IN 14 89177676 89177676 single base substitution C G intron_variant ORCA-IN 14 89178407 89178407 single base substitution G A intron_variant ORCA-IN 14 89179173 89179173 single base substitution G T intron_variant ORCA-IN 14 89181649 89181649 single base substitution A G intron_variant ORCA-IN 14 89181649 89181649 single base substitution A G upstream_gene_variant ORCA-IN 14 89186720 89186720 single base substitution C A intron_variant ORCA-IN 14 89193156 89193156 single base substitution C G intron_variant ORCA-IN 14 89195010 89195010 single base substitution G C intron_variant ORCA-IN 14 89260357 89260357 deletion of <=200bp A - upstream_gene_variant OV-AU 14 89075379 89075379 single base substitution T G downstream_gene_variant OV-AU 14 89080137 89080137 single base substitution A G 3_prime_UTR_variant OV-AU 14 89080137 89080137 single base substitution A G downstream_gene_variant OV-AU 14 89080137 89080137 single base substitution A G exon_variant OV-AU 14 89085021 89085021 single base substitution G C 3_prime_UTR_variant OV-AU 14 89085021 89085021 single base substitution G C downstream_gene_variant OV-AU 14 89085021 89085021 single base substitution G C exon_variant OV-AU 14 89085021 89085021 single base substitution G C missense_variant D1791E 5373C>G OV-AU 14 89085021 89085021 single base substitution G C missense_variant D1829E 5487C>G OV-AU 14 89085021 89085021 single base substitution G C missense_variant D1837E 5511C>G OV-AU 14 89085021 89085021 single base substitution G C missense_variant D247E 741C>G OV-AU 14 89086036 89086036 single base substitution T C downstream_gene_variant OV-AU 14 89086036 89086036 single base substitution T C exon_variant OV-AU 14 89086036 89086036 single base substitution T C intron_variant OV-AU 14 89087894 89087894 single base substitution C A downstream_gene_variant OV-AU 14 89087894 89087894 single base substitution C A intron_variant OV-AU 14 89087894 89087894 single base substitution C A upstream_gene_variant OV-AU 14 89093851 89093851 single base substitution C G downstream_gene_variant OV-AU 14 89093851 89093851 single base substitution C G intron_variant OV-AU 14 89093851 89093851 single base substitution C G upstream_gene_variant OV-AU 14 89097445 89097445 single base substitution C G intron_variant OV-AU 14 89097445 89097445 single base substitution C G upstream_gene_variant OV-AU 14 89103082 89103082 single base substitution T C intron_variant OV-AU 14 89104392 89104392 single base substitution G A intron_variant OV-AU 14 89105063 89105063 single base substitution A C intron_variant OV-AU 14 89107703 89107703 single base substitution C A intron_variant OV-AU 14 89115438 89115438 single base substitution A G intron_variant OV-AU 14 89115438 89115438 single base substitution A G upstream_gene_variant OV-AU 14 89115504 89115504 single base substitution G T intron_variant OV-AU 14 89115504 89115504 single base substitution G T upstream_gene_variant OV-AU 14 89121267 89121267 single base substitution G C intron_variant OV-AU 14 89121503 89121503 single base substitution C A intron_variant OV-AU 14 89122523 89122523 single base substitution A G intron_variant OV-AU 14 89123791 89123791 single base substitution T C 3_prime_UTR_variant OV-AU 14 89123791 89123791 single base substitution T C synonymous_variant L1273L 3819A>G OV-AU 14 89123791 89123791 single base substitution T C synonymous_variant L1311L 3933A>G OV-AU 14 89124585 89124585 single base substitution C G 3_prime_UTR_variant OV-AU 14 89124585 89124585 single base substitution C G missense_variant E1237Q 3709G>C OV-AU 14 89124585 89124585 single base substitution C G missense_variant E1275Q 3823G>C OV-AU 14 89128993 89128993 single base substitution C T intron_variant OV-AU 14 89136670 89136670 single base substitution A C intron_variant OV-AU 14 89136670 89136670 single base substitution A C upstream_gene_variant OV-AU 14 89143650 89143650 single base substitution G T intron_variant OV-AU 14 89144989 89144989 single base substitution T A intron_variant OV-AU 14 89145774 89145774 single base substitution G T intron_variant OV-AU 14 89147818 89147818 single base substitution A G intron_variant OV-AU 14 89149244 89149244 single base substitution T A intron_variant OV-AU 14 89150133 89150133 single base substitution G A intron_variant OV-AU 14 89150133 89150133 single base substitution G T intron_variant OV-AU 14 89157166 89157166 single base substitution A G intron_variant OV-AU 14 89157641 89157641 single base substitution G T intron_variant OV-AU 14 89160792 89160792 single base substitution C T intron_variant OV-AU 14 89162222 89162222 single base substitution T A intron_variant OV-AU 14 89163387 89163387 single base substitution T A intron_variant OV-AU 14 89166301 89166301 single base substitution T C intron_variant OV-AU 14 89169248 89169248 single base substitution G A intron_variant OV-AU 14 89178781 89178781 single base substitution C G exon_variant OV-AU 14 89178781 89178781 single base substitution C G missense_variant W497C 1491G>C OV-AU 14 89180638 89180638 single base substitution A G intron_variant OV-AU 14 89202905 89202905 single base substitution C A missense_variant L284F 852G>T OV-AU 14 89203367 89203367 single base substitution T C intron_variant OV-AU 14 89204259 89204259 single base substitution T A intron_variant OV-AU 14 89204576 89204576 single base substitution T C intron_variant OV-AU 14 89207519 89207519 single base substitution A T intron_variant OV-AU 14 89223447 89223447 single base substitution G C intron_variant OV-AU 14 89224186 89224186 single base substitution C T intron_variant OV-AU 14 89232897 89232897 single base substitution G A intron_variant OV-AU 14 89234756 89234756 single base substitution A G intron_variant OV-AU 14 89237507 89237507 single base substitution G C intron_variant OV-AU 14 89243802 89243802 single base substitution G A intron_variant OV-AU 14 89244728 89244728 single base substitution T G intron_variant OV-AU 14 89259558 89259558 single base substitution G T upstream_gene_variant OV-AU 14 89261268 89261268 single base substitution C T upstream_gene_variant OV-AU 14 89263343 89263343 single base substitution A T upstream_gene_variant OV-US 14 89205266 89205266 single base substitution T C synonymous_variant P268P 804A>G PACA-AU 14 89077644 89077644 single base substitution G T downstream_gene_variant PACA-AU 14 89088948 89088948 single base substitution T G intron_variant PACA-AU 14 89088948 89088948 single base substitution T G missense_variant K112N 336A>C PACA-AU 14 89088948 89088948 single base substitution T G missense_variant K1625N 4875A>C PACA-AU 14 89088948 89088948 single base substitution T G missense_variant K1663N 4989A>C PACA-AU 14 89088948 89088948 single base substitution T G missense_variant K1671N 5013A>C PACA-AU 14 89088948 89088948 single base substitution T G splice_region_variant PACA-AU 14 89088948 89088948 single base substitution T G upstream_gene_variant PACA-AU 14 89097611 89097611 single base substitution G A intron_variant PACA-AU 14 89097611 89097611 single base substitution G A upstream_gene_variant PACA-AU 14 89110199 89110199 single base substitution C T intron_variant PACA-AU 14 89110822 89110822 single base substitution C A 3_prime_UTR_variant PACA-AU 14 89110822 89110822 single base substitution C A exon_variant PACA-AU 14 89110822 89110822 single base substitution C A missense_variant E1308D 3924G>T PACA-AU 14 89110822 89110822 single base substitution C A missense_variant E1346D 4038G>T PACA-AU 14 89110822 89110822 single base substitution C A missense_variant E1354D 4062G>T PACA-AU 14 89116609 89116609 single base substitution C T intron_variant PACA-AU 14 89117502 89117502 single base substitution T C intron_variant PACA-AU 14 89117504 89117504 single base substitution T C intron_variant PACA-AU 14 89118520 89118520 single base substitution A C intron_variant PACA-AU 14 89123949 89123949 single base substitution T A intron_variant PACA-AU 14 89125520 89125520 single base substitution G A intron_variant PACA-AU 14 89138927 89138927 single base substitution G A intron_variant PACA-AU 14 89139274 89139274 single base substitution A G intron_variant PACA-AU 14 89141690 89141690 single base substitution A G intron_variant PACA-AU 14 89141722 89141722 single base substitution C T intron_variant PACA-AU 14 89141735 89141735 single base substitution C T intron_variant PACA-AU 14 89141927 89141927 single base substitution G A intron_variant PACA-AU 14 89142399 89142399 single base substitution C T intron_variant PACA-AU 14 89143826 89143826 single base substitution C T intron_variant PACA-AU 14 89145246 89145246 single base substitution G T intron_variant PACA-AU 14 89148728 89148728 single base substitution C A intron_variant PACA-AU 14 89148956 89148956 single base substitution C A intron_variant PACA-AU 14 89153683 89153683 single base substitution A C intron_variant PACA-AU 14 89154759 89154759 single base substitution C A intron_variant PACA-AU 14 89154759 89154759 single base substitution C A missense_variant M866I 2598G>T PACA-AU 14 89167396 89167396 single base substitution A G intron_variant PACA-AU 14 89168972 89168972 single base substitution T G 3_prime_UTR_variant PACA-AU 14 89168972 89168972 single base substitution T G synonymous_variant R686R 2056A>C PACA-AU 14 89174929 89174929 single base substitution T C intron_variant PACA-AU 14 89176972 89176972 single base substitution T C intron_variant PACA-AU 14 89190353 89190353 single base substitution G A intron_variant PACA-AU 14 89195907 89195909 deletion of <=200bp TTG - intron_variant PACA-AU 14 89197227 89197227 single base substitution T G intron_variant PACA-AU 14 89199022 89199022 insertion of <=200bp - T intron_variant PACA-AU 14 89200039 89200039 single base substitution C A intron_variant PACA-AU 14 89200690 89200690 single base substitution C T intron_variant PACA-AU 14 89205267 89205267 single base substitution G C missense_variant P268R 803C>G PACA-AU 14 89206069 89206069 single base substitution T C intron_variant PACA-AU 14 89211068 89211068 single base substitution A C intron_variant PACA-AU 14 89215415 89215415 single base substitution A C intron_variant PACA-AU 14 89216689 89216689 single base substitution C A intron_variant PACA-AU 14 89218431 89218431 single base substitution A C intron_variant PACA-AU 14 89222589 89222589 single base substitution C A intron_variant PACA-AU 14 89223515 89223515 single base substitution A G intron_variant PACA-AU 14 89226036 89226036 single base substitution A C intron_variant PACA-AU 14 89231252 89231252 single base substitution T G intron_variant PACA-AU 14 89232429 89232429 single base substitution C A intron_variant PACA-AU 14 89232508 89232508 single base substitution C T intron_variant PACA-AU 14 89232924 89232924 single base substitution C T intron_variant PACA-AU 14 89239416 89239416 single base substitution T G intron_variant PACA-AU 14 89241292 89241292 single base substitution G A intron_variant PACA-AU 14 89246056 89246056 single base substitution T C intron_variant PACA-AU 14 89250200 89250200 single base substitution G A intron_variant PACA-AU 14 89251807 89251807 single base substitution C G intron_variant PACA-CA 14 89075375 89075375 single base substitution T A downstream_gene_variant PACA-CA 14 89075976 89075976 insertion of <=200bp - A downstream_gene_variant PACA-CA 14 89075977 89075977 deletion of <=200bp A - downstream_gene_variant PACA-CA 14 89077449 89077449 single base substitution T C downstream_gene_variant PACA-CA 14 89081212 89081212 insertion of <=200bp - A 3_prime_UTR_variant PACA-CA 14 89081212 89081212 insertion of <=200bp - A downstream_gene_variant PACA-CA 14 89081212 89081212 insertion of <=200bp - A exon_variant PACA-CA 14 89081931 89081931 single base substitution C T 3_prime_UTR_variant PACA-CA 14 89081931 89081931 single base substitution C T downstream_gene_variant PACA-CA 14 89081931 89081931 single base substitution C T exon_variant PACA-CA 14 89087729 89087729 single base substitution C A downstream_gene_variant PACA-CA 14 89087729 89087729 single base substitution C A intron_variant PACA-CA 14 89087729 89087729 single base substitution C A upstream_gene_variant PACA-CA 14 89092305 89092305 single base substitution G T downstream_gene_variant PACA-CA 14 89092305 89092305 single base substitution G T intron_variant PACA-CA 14 89100013 89100013 single base substitution C A intron_variant PACA-CA 14 89103627 89103627 single base substitution C T intron_variant PACA-CA 14 89106350 89106350 single base substitution A T intron_variant PACA-CA 14 89113594 89113594 single base substitution T A intron_variant PACA-CA 14 89113594 89113594 single base substitution T A upstream_gene_variant PACA-CA 14 89115499 89115499 single base substitution G T intron_variant PACA-CA 14 89115499 89115499 single base substitution G T upstream_gene_variant PACA-CA 14 89116061 89116061 single base substitution G C intron_variant PACA-CA 14 89116061 89116061 single base substitution G C upstream_gene_variant PACA-CA 14 89117891 89117891 insertion of <=200bp - T intron_variant PACA-CA 14 89124850 89124850 deletion of <=200bp A - intron_variant PACA-CA 14 89125602 89125602 single base substitution C G intron_variant PACA-CA 14 89126539 89126539 single base substitution A T intron_variant PACA-CA 14 89126861 89126861 single base substitution C T intron_variant PACA-CA 14 89135555 89135555 single base substitution C T intron_variant PACA-CA 14 89135555 89135555 single base substitution C T upstream_gene_variant PACA-CA 14 89137955 89137955 single base substitution C G intron_variant PACA-CA 14 89140741 89140741 single base substitution C A intron_variant PACA-CA 14 89149323 89149323 single base substitution T A intron_variant PACA-CA 14 89149604 89149604 single base substitution T C intron_variant PACA-CA 14 89150420 89150420 single base substitution A G intron_variant PACA-CA 14 89159446 89159446 single base substitution A G intron_variant PACA-CA 14 89160981 89160981 single base substitution C T intron_variant PACA-CA 14 89171654 89171654 insertion of <=200bp - A intron_variant PACA-CA 14 89173614 89173614 single base substitution T C intron_variant PACA-CA 14 89174673 89174673 deletion of <=200bp C - intron_variant PACA-CA 14 89177957 89177957 single base substitution C T intron_variant PACA-CA 14 89178563 89178563 single base substitution C T intron_variant PACA-CA 14 89178958 89178958 single base substitution A C intron_variant PACA-CA 14 89179068 89179068 single base substitution T A intron_variant PACA-CA 14 89182787 89182795 deletion of <=200bp CCCTTTGCT - intron_variant PACA-CA 14 89182787 89182795 deletion of <=200bp CCCTTTGCT - upstream_gene_variant PACA-CA 14 89183915 89183915 single base substitution C T intron_variant PACA-CA 14 89183915 89183915 single base substitution C T upstream_gene_variant PACA-CA 14 89186168 89186168 single base substitution C T intron_variant PACA-CA 14 89186168 89186168 single base substitution C T upstream_gene_variant PACA-CA 14 89201433 89201433 single base substitution A T intron_variant PACA-CA 14 89202197 89202197 single base substitution A G intron_variant PACA-CA 14 89203869 89203869 single base substitution G A intron_variant PACA-CA 14 89206319 89206319 single base substitution C T intron_variant PACA-CA 14 89206950 89206950 single base substitution G C intron_variant PACA-CA 14 89207520 89207520 single base substitution T A intron_variant PACA-CA 14 89210640 89210640 single base substitution T C intron_variant PACA-CA 14 89211973 89211973 single base substitution C G intron_variant PACA-CA 14 89220465 89220465 single base substitution G A intron_variant PACA-CA 14 89225905 89225905 single base substitution G A intron_variant PACA-CA 14 89227868 89227868 single base substitution A T intron_variant PACA-CA 14 89229416 89229416 single base substitution G T intron_variant PACA-CA 14 89229780 89229780 single base substitution C A intron_variant PACA-CA 14 89230205 89230205 single base substitution T G intron_variant PACA-CA 14 89233248 89233248 single base substitution G A intron_variant PACA-CA 14 89233495 89233495 single base substitution A C intron_variant PACA-CA 14 89233552 89233552 single base substitution T G intron_variant PACA-CA 14 89234091 89234091 single base substitution G A intron_variant PACA-CA 14 89237581 89237581 insertion of <=200bp - C intron_variant PACA-CA 14 89237976 89237976 single base substitution A T intron_variant PACA-CA 14 89239545 89239545 single base substitution C A intron_variant PACA-CA 14 89241073 89241073 single base substitution A T intron_variant PACA-CA 14 89241295 89241295 single base substitution C A intron_variant PACA-CA 14 89244153 89244153 single base substitution T C intron_variant PACA-CA 14 89247522 89247522 single base substitution C T intron_variant PACA-CA 14 89247920 89247920 single base substitution C G intron_variant PACA-CA 14 89250711 89250711 single base substitution T A intron_variant PACA-CA 14 89252075 89252075 single base substitution T G intron_variant PACA-CA 14 89252567 89252567 single base substitution C A intron_variant PACA-CA 14 89252900 89252900 single base substitution G T intron_variant PACA-CA 14 89253711 89253711 single base substitution G C intron_variant PACA-CA 14 89255775 89255775 single base substitution G A intron_variant PACA-CA 14 89257377 89257377 single base substitution C A intron_variant PACA-CA 14 89260054 89260054 single base substitution G C upstream_gene_variant PACA-CA 14 89261407 89261407 single base substitution A T upstream_gene_variant PACA-CA 14 89263446 89263446 single base substitution T A upstream_gene_variant PAEN-AU 14 89074212 89074212 single base substitution A C downstream_gene_variant PAEN-AU 14 89095518 89095518 single base substitution C G intron_variant PAEN-AU 14 89095518 89095518 single base substitution C G upstream_gene_variant PAEN-AU 14 89112474 89112474 single base substitution C G intron_variant PAEN-AU 14 89112474 89112474 single base substitution C G upstream_gene_variant PAEN-AU 14 89139762 89139762 single base substitution T G intron_variant PAEN-AU 14 89196923 89196923 single base substitution C T intron_variant PAEN-AU 14 89222363 89222363 single base substitution A G intron_variant PAEN-AU 14 89230340 89230340 single base substitution G C intron_variant PAEN-AU 14 89243630 89243630 single base substitution T A intron_variant PAEN-AU 14 89253554 89253554 single base substitution G T intron_variant PAEN-IT 14 89123056 89123056 single base substitution G C intron_variant PAEN-IT 14 89142934 89142934 single base substitution T C intron_variant PAEN-IT 14 89166311 89166311 single base substitution C T intron_variant PAEN-IT 14 89217289 89217289 single base substitution C A intron_variant PBCA-DE 14 89074206 89074206 deletion of <=200bp T - downstream_gene_variant PBCA-DE 14 89074327 89074327 insertion of <=200bp - AGTG downstream_gene_variant PBCA-DE 14 89075150 89075150 insertion of <=200bp - T downstream_gene_variant PBCA-DE 14 89081425 89081425 single base substitution T C 3_prime_UTR_variant PBCA-DE 14 89081425 89081425 single base substitution T C downstream_gene_variant PBCA-DE 14 89081425 89081425 single base substitution T C exon_variant PBCA-DE 14 89081630 89081630 single base substitution A T 3_prime_UTR_variant PBCA-DE 14 89081630 89081630 single base substitution A T downstream_gene_variant PBCA-DE 14 89081630 89081630 single base substitution A T exon_variant PBCA-DE 14 89083469 89083469 single base substitution A T downstream_gene_variant PBCA-DE 14 89083469 89083469 single base substitution A T intron_variant PBCA-DE 14 89086111 89086111 single base substitution C T downstream_gene_variant PBCA-DE 14 89086111 89086111 single base substitution C T intron_variant PBCA-DE 14 89086111 89086111 single base substitution C T upstream_gene_variant PBCA-DE 14 89102911 89102911 single base substitution A C intron_variant PBCA-DE 14 89113721 89113721 insertion of <=200bp - A intron_variant PBCA-DE 14 89113721 89113721 insertion of <=200bp - A upstream_gene_variant PBCA-DE 14 89115814 89115814 single base substitution C A intron_variant PBCA-DE 14 89115814 89115814 single base substitution C A upstream_gene_variant PBCA-DE 14 89128631 89128631 insertion of <=200bp - A intron_variant PBCA-DE 14 89130495 89130495 single base substitution G A intron_variant PBCA-DE 14 89131136 89131136 single base substitution T A intron_variant PBCA-DE 14 89131368 89131368 single base substitution G T intron_variant PBCA-DE 14 89138067 89138067 single base substitution G T intron_variant PBCA-DE 14 89138125 89138125 insertion of <=200bp - A intron_variant PBCA-DE 14 89154685 89154685 single base substitution C T 3_prime_UTR_variant PBCA-DE 14 89154685 89154685 single base substitution C T missense_variant R853K 2558G>A PBCA-DE 14 89154685 89154685 single base substitution C T missense_variant R891K 2672G>A PBCA-DE 14 89158159 89158159 single base substitution A T intron_variant PBCA-DE 14 89160885 89160885 single base substitution G A intron_variant PBCA-DE 14 89165638 89165638 insertion of <=200bp - A intron_variant PBCA-DE 14 89167301 89167301 insertion of <=200bp - T intron_variant PBCA-DE 14 89167470 89167470 single base substitution C A intron_variant PBCA-DE 14 89171710 89171710 single base substitution T C intron_variant PBCA-DE 14 89173615 89173615 insertion of <=200bp - TTTA intron_variant PBCA-DE 14 89184085 89184085 single base substitution C T intron_variant PBCA-DE 14 89184085 89184085 single base substitution C T upstream_gene_variant PBCA-DE 14 89186900 89186900 single base substitution C T intron_variant PBCA-DE 14 89201170 89201170 single base substitution G A intron_variant PBCA-DE 14 89205429 89205429 single base substitution C T intron_variant PBCA-DE 14 89217870 89217870 insertion of <=200bp - T intron_variant PBCA-DE 14 89222184 89222184 single base substitution T A intron_variant PBCA-DE 14 89239140 89239140 single base substitution C G intron_variant PBCA-DE 14 89253921 89253921 single base substitution C T intron_variant PBCA-DE 14 89258872 89258872 single base substitution C G 5_prime_UTR_variant PBCA-DE 14 89258872 89258872 single base substitution C G upstream_gene_variant PRAD-CA 14 89104258 89104258 single base substitution T C intron_variant PRAD-CA 14 89105053 89105053 single base substitution T G intron_variant PRAD-CA 14 89136392 89136392 single base substitution G A intron_variant PRAD-CA 14 89136392 89136392 single base substitution G A upstream_gene_variant PRAD-CA 14 89139672 89139672 single base substitution A C intron_variant PRAD-CA 14 89149908 89149908 single base substitution A C intron_variant PRAD-CA 14 89180877 89180877 single base substitution G A intron_variant PRAD-CA 14 89210835 89210835 single base substitution T C intron_variant PRAD-CA 14 89239428 89239428 single base substitution C G intron_variant PRAD-CA 14 89263059 89263059 single base substitution A G upstream_gene_variant PRAD-UK 14 89090411 89090411 insertion of <=200bp - T downstream_gene_variant PRAD-UK 14 89090411 89090411 insertion of <=200bp - T intron_variant PRAD-UK 14 89090411 89090411 insertion of <=200bp - T upstream_gene_variant PRAD-UK 14 89101746 89101746 deletion of <=200bp C - intron_variant PRAD-UK 14 89106770 89106770 single base substitution T A intron_variant PRAD-UK 14 89166621 89166621 insertion of <=200bp - A intron_variant PRAD-UK 14 89182379 89182379 single base substitution C A intron_variant PRAD-UK 14 89182379 89182379 single base substitution C A upstream_gene_variant PRAD-UK 14 89197711 89197711 single base substitution T C intron_variant PRAD-UK 14 89197712 89197712 single base substitution C T intron_variant PRAD-UK 14 89200742 89200742 single base substitution C T intron_variant PRAD-UK 14 89203854 89203854 single base substitution G A intron_variant PRAD-UK 14 89205960 89205960 single base substitution T A intron_variant PRAD-UK 14 89213611 89213611 single base substitution C T intron_variant PRAD-UK 14 89224657 89224657 single base substitution C T intron_variant PRAD-UK 14 89234515 89234515 single base substitution G A intron_variant PRAD-UK 14 89246377 89246377 single base substitution C G intron_variant PRAD-UK 14 89255244 89255244 single base substitution A G intron_variant PRAD-UK 14 89255481 89255481 insertion of <=200bp - T intron_variant PRAD-UK 14 89256323 89256323 single base substitution A G intron_variant PRAD-US 14 89083083 89083083 single base substitution C T 3_prime_UTR_variant PRAD-US 14 89083083 89083083 single base substitution C T downstream_gene_variant PRAD-US 14 89083083 89083083 single base substitution C T exon_variant PRAD-US 14 89083083 89083083 single base substitution C T missense_variant C1882Y 5645G>A PRAD-US 14 89083083 89083083 single base substitution C T missense_variant C1920Y 5759G>A PRAD-US 14 89083083 89083083 single base substitution C T missense_variant C1928Y 5783G>A PRAD-US 14 89168815 89168815 single base substitution A G 3_prime_UTR_variant PRAD-US 14 89168815 89168815 single base substitution A G missense_variant L738S 2213T>C READ-US 14 89077271 89077271 single base substitution C T downstream_gene_variant READ-US 14 89088968 89088968 single base substitution G A 3_prime_UTR_variant READ-US 14 89088968 89088968 single base substitution G A intron_variant READ-US 14 89088968 89088968 single base substitution G A missense_variant R106C 316C>T READ-US 14 89088968 89088968 single base substitution G A missense_variant R1619C 4855C>T READ-US 14 89088968 89088968 single base substitution G A missense_variant R1657C 4969C>T READ-US 14 89088968 89088968 single base substitution G A missense_variant R1665C 4993C>T READ-US 14 89088968 89088968 single base substitution G A upstream_gene_variant READ-US 14 89131752 89131752 single base substitution G A 3_prime_UTR_variant READ-US 14 89131752 89131752 single base substitution G A missense_variant A1031V 3092C>T READ-US 14 89131752 89131752 single base substitution G A missense_variant A1069V 3206C>T READ-US 14 89131752 89131752 single base substitution G A upstream_gene_variant READ-US 14 89154718 89154718 single base substitution G A intron_variant READ-US 14 89154718 89154718 single base substitution G A missense_variant S880F 2639C>T READ-US 14 89168956 89168956 single base substitution C A 3_prime_UTR_variant READ-US 14 89168956 89168956 single base substitution C A missense_variant R691L 2072G>T READ-US 14 89212550 89212550 single base substitution C A missense_variant M145I 435G>T RECA-EU 14 89082580 89082580 single base substitution G A 3_prime_UTR_variant RECA-EU 14 89082580 89082580 single base substitution G A downstream_gene_variant RECA-EU 14 89082580 89082580 single base substitution G A exon_variant RECA-EU 14 89082580 89082580 single base substitution G A missense_variant H1889Y 5665C>T RECA-EU 14 89082580 89082580 single base substitution G A missense_variant H1927Y 5779C>T RECA-EU 14 89082580 89082580 single base substitution G A missense_variant H1935Y 5803C>T RECA-EU 14 89085659 89085659 single base substitution A G downstream_gene_variant RECA-EU 14 89085659 89085659 single base substitution A G exon_variant RECA-EU 14 89085659 89085659 single base substitution A G intron_variant RECA-EU 14 89092316 89092316 single base substitution G T downstream_gene_variant RECA-EU 14 89092316 89092316 single base substitution G T intron_variant RECA-EU 14 89105425 89105425 single base substitution A G intron_variant RECA-EU 14 89120476 89120476 single base substitution C G intron_variant RECA-EU 14 89127526 89127526 single base substitution G A intron_variant RECA-EU 14 89136862 89136862 single base substitution A G intron_variant RECA-EU 14 89144571 89144571 single base substitution G C intron_variant RECA-EU 14 89150927 89150927 single base substitution A T intron_variant RECA-EU 14 89151223 89151223 single base substitution A T intron_variant RECA-EU 14 89156606 89156606 single base substitution T G intron_variant RECA-EU 14 89164432 89164432 single base substitution T G intron_variant RECA-EU 14 89169173 89169173 single base substitution C T intron_variant RECA-EU 14 89172263 89172263 single base substitution T C intron_variant RECA-EU 14 89176622 89176622 single base substitution T G intron_variant RECA-EU 14 89180230 89180230 single base substitution G A intron_variant RECA-EU 14 89187400 89187400 single base substitution G T intron_variant RECA-EU 14 89191177 89191177 single base substitution T A intron_variant RECA-EU 14 89194457 89194457 single base substitution G A intron_variant RECA-EU 14 89206870 89206870 single base substitution A G missense_variant F191S 572T>C RECA-EU 14 89207302 89207302 single base substitution T C intron_variant RECA-EU 14 89214883 89214883 single base substitution C G intron_variant RECA-EU 14 89234044 89234044 single base substitution A G intron_variant RECA-EU 14 89238855 89238855 single base substitution T A intron_variant RECA-EU 14 89246427 89246427 single base substitution C T intron_variant RECA-EU 14 89250710 89250710 single base substitution T A intron_variant RECA-EU 14 89251012 89251012 single base substitution G C intron_variant RECA-EU 14 89251924 89251924 single base substitution C T intron_variant RECA-EU 14 89254778 89254778 single base substitution T C intron_variant RECA-EU 14 89261125 89261125 single base substitution A T upstream_gene_variant SKCA-BR 14 89075999 89075999 single base substitution A T downstream_gene_variant SKCA-BR 14 89076001 89076001 single base substitution T A downstream_gene_variant SKCA-BR 14 89083444 89083444 single base substitution C T downstream_gene_variant SKCA-BR 14 89083444 89083444 single base substitution C T intron_variant SKCA-BR 14 89083749 89083749 single base substitution C T downstream_gene_variant SKCA-BR 14 89083749 89083749 single base substitution C T intron_variant SKCA-BR 14 89087278 89087278 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 14 89087278 89087278 insertion of <=200bp - TA intron_variant SKCA-BR 14 89087278 89087278 insertion of <=200bp - TA splice_region_variant SKCA-BR 14 89087278 89087278 insertion of <=200bp - TA upstream_gene_variant SKCA-BR 14 89087873 89087873 single base substitution G T downstream_gene_variant SKCA-BR 14 89087873 89087873 single base substitution G T intron_variant SKCA-BR 14 89087873 89087873 single base substitution G T upstream_gene_variant SKCA-BR 14 89091087 89091087 single base substitution C T downstream_gene_variant SKCA-BR 14 89091087 89091087 single base substitution C T intron_variant SKCA-BR 14 89091202 89091202 insertion of <=200bp - GGAA downstream_gene_variant SKCA-BR 14 89091202 89091202 insertion of <=200bp - GGAA intron_variant SKCA-BR 14 89092377 89092377 single base substitution G A downstream_gene_variant SKCA-BR 14 89092377 89092377 single base substitution G A intron_variant SKCA-BR 14 89096085 89096085 single base substitution G A intron_variant SKCA-BR 14 89096085 89096085 single base substitution G A upstream_gene_variant SKCA-BR 14 89097643 89097643 single base substitution G A intron_variant SKCA-BR 14 89097643 89097643 single base substitution G A upstream_gene_variant SKCA-BR 14 89100018 89100018 single base substitution C T intron_variant SKCA-BR 14 89100966 89100966 single base substitution A G intron_variant SKCA-BR 14 89101683 89101683 single base substitution G A intron_variant SKCA-BR 14 89105986 89105986 single base substitution T A intron_variant SKCA-BR 14 89107999 89107999 single base substitution G A intron_variant SKCA-BR 14 89108348 89108348 single base substitution G A intron_variant SKCA-BR 14 89112089 89112089 single base substitution G A intron_variant SKCA-BR 14 89112089 89112089 single base substitution G A upstream_gene_variant SKCA-BR 14 89112127 89112127 single base substitution C T intron_variant SKCA-BR 14 89112127 89112127 single base substitution C T upstream_gene_variant SKCA-BR 14 89112722 89112722 single base substitution C G intron_variant SKCA-BR 14 89112722 89112722 single base substitution C G upstream_gene_variant SKCA-BR 14 89113946 89113946 single base substitution G A intron_variant SKCA-BR 14 89113946 89113946 single base substitution G A upstream_gene_variant SKCA-BR 14 89116718 89116718 single base substitution A G intron_variant SKCA-BR 14 89116943 89116943 single base substitution G A intron_variant SKCA-BR 14 89118283 89118283 single base substitution G A intron_variant SKCA-BR 14 89119212 89119212 single base substitution G A intron_variant SKCA-BR 14 89121699 89121699 single base substitution C T intron_variant SKCA-BR 14 89122750 89122750 single base substitution G A intron_variant SKCA-BR 14 89123824 89123824 single base substitution C T 3_prime_UTR_variant SKCA-BR 14 89123824 89123824 single base substitution C T synonymous_variant R1262R 3786G>A SKCA-BR 14 89123824 89123824 single base substitution C T synonymous_variant R1300R 3900G>A SKCA-BR 14 89124423 89124423 single base substitution C T intron_variant SKCA-BR 14 89124740 89124740 single base substitution G A splice_region_variant SKCA-BR 14 89125032 89125032 single base substitution A G intron_variant SKCA-BR 14 89125776 89125776 single base substitution G A intron_variant SKCA-BR 14 89126626 89126626 insertion of <=200bp - TA intron_variant SKCA-BR 14 89127092 89127092 insertion of <=200bp - AAAAAAAG intron_variant SKCA-BR 14 89127274 89127278 deletion of <=200bp CAATG - intron_variant SKCA-BR 14 89129698 89129698 single base substitution G A intron_variant SKCA-BR 14 89132995 89132995 single base substitution C T intron_variant SKCA-BR 14 89132995 89132995 single base substitution C T upstream_gene_variant SKCA-BR 14 89136663 89136663 insertion of <=200bp - CA intron_variant SKCA-BR 14 89136663 89136663 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 14 89137307 89137307 single base substitution G A intron_variant SKCA-BR 14 89138676 89138676 single base substitution A C intron_variant SKCA-BR 14 89139856 89139856 single base substitution G A intron_variant SKCA-BR 14 89139912 89139912 single base substitution G A intron_variant SKCA-BR 14 89140073 89140073 single base substitution C T intron_variant SKCA-BR 14 89140165 89140165 single base substitution G A intron_variant SKCA-BR 14 89141287 89141287 single base substitution G A intron_variant SKCA-BR 14 89141892 89141892 single base substitution C T intron_variant SKCA-BR 14 89143044 89143044 single base substitution G A intron_variant SKCA-BR 14 89143753 89143753 single base substitution G A intron_variant SKCA-BR 14 89143847 89143847 single base substitution G A intron_variant SKCA-BR 14 89146919 89146919 single base substitution G A intron_variant SKCA-BR 14 89148336 89148336 single base substitution G A 3_prime_UTR_variant SKCA-BR 14 89148336 89148336 single base substitution G A missense_variant P1008S 3022C>T SKCA-BR 14 89148336 89148336 single base substitution G A missense_variant P970S 2908C>T SKCA-BR 14 89150873 89150873 insertion of <=200bp - ACATT intron_variant SKCA-BR 14 89153068 89153068 single base substitution C T intron_variant SKCA-BR 14 89153736 89153736 single base substitution C T intron_variant SKCA-BR 14 89157226 89157226 single base substitution G A intron_variant SKCA-BR 14 89157787 89157787 single base substitution C T intron_variant SKCA-BR 14 89158696 89158696 single base substitution G A intron_variant SKCA-BR 14 89160584 89160584 single base substitution G A intron_variant SKCA-BR 14 89161518 89161518 single base substitution G A intron_variant SKCA-BR 14 89164824 89164824 single base substitution G A intron_variant SKCA-BR 14 89165460 89165460 single base substitution G A intron_variant SKCA-BR 14 89166355 89166355 single base substitution C G intron_variant SKCA-BR 14 89171539 89171539 single base substitution G A intron_variant SKCA-BR 14 89171727 89171727 single base substitution A C intron_variant SKCA-BR 14 89172758 89172758 single base substitution C T exon_variant SKCA-BR 14 89172758 89172758 single base substitution C T missense_variant R557K 1670G>A SKCA-BR 14 89172907 89172907 single base substitution T C intron_variant SKCA-BR 14 89173614 89173614 insertion of <=200bp - TTTTA intron_variant SKCA-BR 14 89177826 89177826 single base substitution G A intron_variant SKCA-BR 14 89177906 89177906 single base substitution G A intron_variant SKCA-BR 14 89178286 89178287 deletion of <=200bp CA - intron_variant SKCA-BR 14 89179723 89179723 single base substitution G A intron_variant SKCA-BR 14 89183351 89183351 single base substitution G A intron_variant SKCA-BR 14 89183351 89183351 single base substitution G A upstream_gene_variant SKCA-BR 14 89185624 89185624 single base substitution G A intron_variant SKCA-BR 14 89185624 89185624 single base substitution G A upstream_gene_variant SKCA-BR 14 89185671 89185678 deletion of <=200bp AGTGAGCT - intron_variant SKCA-BR 14 89185671 89185678 deletion of <=200bp AGTGAGCT - upstream_gene_variant SKCA-BR 14 89186260 89186260 single base substitution G A intron_variant SKCA-BR 14 89186260 89186260 single base substitution G A upstream_gene_variant SKCA-BR 14 89187121 89187121 single base substitution G A intron_variant SKCA-BR 14 89187168 89187168 single base substitution G A intron_variant SKCA-BR 14 89187599 89187599 single base substitution G A intron_variant SKCA-BR 14 89188809 89188809 single base substitution G C intron_variant SKCA-BR 14 89189201 89189201 single base substitution C T intron_variant SKCA-BR 14 89190458 89190458 insertion of <=200bp - CAA intron_variant SKCA-BR 14 89190458 89190458 insertion of <=200bp - CA intron_variant SKCA-BR 14 89192291 89192291 single base substitution C T intron_variant SKCA-BR 14 89193416 89193416 single base substitution C T intron_variant SKCA-BR 14 89193625 89193625 single base substitution C T intron_variant SKCA-BR 14 89193735 89193735 single base substitution G A intron_variant SKCA-BR 14 89193745 89193745 insertion of <=200bp - ATT intron_variant SKCA-BR 14 89197855 89197855 single base substitution T C intron_variant SKCA-BR 14 89197894 89197894 single base substitution G A intron_variant SKCA-BR 14 89198241 89198241 single base substitution C T intron_variant SKCA-BR 14 89199636 89199636 single base substitution G A intron_variant SKCA-BR 14 89199637 89199637 single base substitution G A intron_variant SKCA-BR 14 89202218 89202218 single base substitution G A intron_variant SKCA-BR 14 89203725 89203725 single base substitution G A intron_variant SKCA-BR 14 89203929 89203929 single base substitution C T intron_variant SKCA-BR 14 89204804 89204804 single base substitution G A intron_variant SKCA-BR 14 89204835 89204835 single base substitution C T intron_variant SKCA-BR 14 89205422 89205422 single base substitution T G intron_variant SKCA-BR 14 89214168 89214168 single base substitution T A intron_variant SKCA-BR 14 89214176 89214176 single base substitution C A intron_variant SKCA-BR 14 89215962 89215962 single base substitution G A intron_variant SKCA-BR 14 89220890 89220890 single base substitution C T missense_variant G108D 323G>A SKCA-BR 14 89222148 89222148 single base substitution G A intron_variant SKCA-BR 14 89224004 89224004 single base substitution G A intron_variant SKCA-BR 14 89225579 89225579 single base substitution G A intron_variant SKCA-BR 14 89228859 89228859 single base substitution G A intron_variant SKCA-BR 14 89228980 89228980 single base substitution G A intron_variant SKCA-BR 14 89229148 89229148 single base substitution A C intron_variant SKCA-BR 14 89229838 89229838 single base substitution G A intron_variant SKCA-BR 14 89230158 89230158 single base substitution C T intron_variant SKCA-BR 14 89230475 89230475 single base substitution G A intron_variant SKCA-BR 14 89232393 89232393 single base substitution C T intron_variant SKCA-BR 14 89234773 89234773 single base substitution G T intron_variant SKCA-BR 14 89236338 89236338 single base substitution T A intron_variant SKCA-BR 14 89236874 89236874 single base substitution G A intron_variant SKCA-BR 14 89237240 89237240 single base substitution G A intron_variant SKCA-BR 14 89237284 89237284 single base substitution G A intron_variant SKCA-BR 14 89237858 89237858 single base substitution C A intron_variant SKCA-BR 14 89237918 89237918 single base substitution A G intron_variant SKCA-BR 14 89239677 89239677 single base substitution C T intron_variant SKCA-BR 14 89239917 89239917 single base substitution C T intron_variant SKCA-BR 14 89240210 89240210 single base substitution C T intron_variant SKCA-BR 14 89241412 89241412 single base substitution C A intron_variant SKCA-BR 14 89242122 89242122 single base substitution G A intron_variant SKCA-BR 14 89244567 89244567 single base substitution G A intron_variant SKCA-BR 14 89245690 89245690 single base substitution G A intron_variant SKCA-BR 14 89247139 89247139 single base substitution G A intron_variant SKCA-BR 14 89248211 89248211 single base substitution G A intron_variant SKCA-BR 14 89250505 89250505 single base substitution G A intron_variant SKCA-BR 14 89252133 89252133 single base substitution C T intron_variant SKCA-BR 14 89252720 89252720 single base substitution A C intron_variant SKCA-BR 14 89259926 89259926 single base substitution T G upstream_gene_variant SKCA-BR 14 89259930 89259930 single base substitution G T upstream_gene_variant SKCA-BR 14 89262470 89262470 single base substitution A C upstream_gene_variant SKCA-BR 14 89262554 89262556 deletion of <=200bp TTA - upstream_gene_variant SKCA-BR 14 89262556 89262572 deletion of <=200bp ATATATATATTATATGT - upstream_gene_variant SKCA-BR 14 89263250 89263250 single base substitution T C upstream_gene_variant SKCA-BR 14 89263686 89263688 deletion of <=200bp TTC - upstream_gene_variant SKCM-US 14 89083224 89083224 single base substitution C T downstream_gene_variant SKCM-US 14 89083224 89083224 single base substitution C T splice_acceptor_variant SKCM-US 14 89091324 89091324 single base substitution T A 3_prime_UTR_variant SKCM-US 14 89091324 89091324 single base substitution T A downstream_gene_variant SKCM-US 14 89091324 89091324 single base substitution T A exon_variant SKCM-US 14 89091324 89091324 single base substitution T A stop_gained K1584* 4750A>T SKCM-US 14 89091324 89091324 single base substitution T A stop_gained K1622* 4864A>T SKCM-US 14 89091324 89091324 single base substitution T A stop_gained K1630* 4888A>T SKCM-US 14 89091324 89091324 single base substitution T A stop_gained K71* 211A>T SKCM-US 14 89093244 89093244 single base substitution C T 3_prime_UTR_variant SKCM-US 14 89093244 89093244 single base substitution C T downstream_gene_variant SKCM-US 14 89093244 89093244 single base substitution C T exon_variant SKCM-US 14 89093244 89093244 single base substitution C T missense_variant G1514R 4540G>A SKCM-US 14 89093244 89093244 single base substitution C T missense_variant G1552R 4654G>A SKCM-US 14 89093244 89093244 single base substitution C T missense_variant G1560R 4678G>A SKCM-US 14 89093244 89093244 single base substitution C T missense_variant G1R 1G>A SKCM-US 14 89093316 89093316 single base substitution G C 3_prime_UTR_variant SKCM-US 14 89093316 89093316 single base substitution G C downstream_gene_variant SKCM-US 14 89093316 89093316 single base substitution G C missense_variant Q1490E 4468C>G SKCM-US 14 89093316 89093316 single base substitution G C missense_variant Q1528E 4582C>G SKCM-US 14 89093316 89093316 single base substitution G C missense_variant Q1536E 4606C>G SKCM-US 14 89093316 89093316 single base substitution G C upstream_gene_variant SKCM-US 14 89093343 89093343 single base substitution C T 3_prime_UTR_variant SKCM-US 14 89093343 89093343 single base substitution C T downstream_gene_variant SKCM-US 14 89093343 89093343 single base substitution C T missense_variant A1481T 4441G>A SKCM-US 14 89093343 89093343 single base substitution C T missense_variant A1519T 4555G>A SKCM-US 14 89093343 89093343 single base substitution C T missense_variant A1527T 4579G>A SKCM-US 14 89093343 89093343 single base substitution C T upstream_gene_variant SKCM-US 14 89094155 89094155 single base substitution G A 3_prime_UTR_variant SKCM-US 14 89094155 89094155 single base substitution G A exon_variant SKCM-US 14 89094155 89094155 single base substitution G A missense_variant P1410S 4228C>T SKCM-US 14 89094155 89094155 single base substitution G A missense_variant P1448S 4342C>T SKCM-US 14 89094155 89094155 single base substitution G A missense_variant P1456S 4366C>T SKCM-US 14 89094155 89094155 single base substitution G A upstream_gene_variant SKCM-US 14 89109309 89109309 single base substitution G A 3_prime_UTR_variant SKCM-US 14 89109309 89109309 single base substitution G A exon_variant SKCM-US 14 89109309 89109309 single base substitution G A missense_variant H1343Y 4027C>T SKCM-US 14 89109309 89109309 single base substitution G A missense_variant H1381Y 4141C>T SKCM-US 14 89109309 89109309 single base substitution G A missense_variant H1389Y 4165C>T SKCM-US 14 89123778 89123778 single base substitution G A 3_prime_UTR_variant SKCM-US 14 89123778 89123778 single base substitution G A missense_variant R1278C 3832C>T SKCM-US 14 89123778 89123778 single base substitution G A missense_variant R1316C 3946C>T SKCM-US 14 89131692 89131692 single base substitution C T 3_prime_UTR_variant SKCM-US 14 89131692 89131692 single base substitution C T exon_variant SKCM-US 14 89131692 89131692 single base substitution C T missense_variant R1051Q 3152G>A SKCM-US 14 89131692 89131692 single base substitution C T missense_variant R1089Q 3266G>A SKCM-US 14 89131701 89131701 single base substitution G A 3_prime_UTR_variant SKCM-US 14 89131701 89131701 single base substitution G A exon_variant SKCM-US 14 89131701 89131701 single base substitution G A missense_variant S1048L 3143C>T SKCM-US 14 89131701 89131701 single base substitution G A missense_variant S1086L 3257C>T SKCM-US 14 89148295 89148295 single base substitution G A 3_prime_UTR_variant SKCM-US 14 89148295 89148295 single base substitution G A synonymous_variant T1021T 3063C>T SKCM-US 14 89148295 89148295 single base substitution G A synonymous_variant T983T 2949C>T SKCM-US 14 89151388 89151388 single base substitution T C 3_prime_UTR_variant SKCM-US 14 89151388 89151388 single base substitution T C missense_variant K947E 2839A>G SKCM-US 14 89151388 89151388 single base substitution T C missense_variant K985E 2953A>G SKCM-US 14 89153569 89153569 single base substitution C T 3_prime_UTR_variant SKCM-US 14 89153569 89153569 single base substitution C T missense_variant G911R 2731G>A SKCM-US 14 89153569 89153569 single base substitution C T missense_variant G949R 2845G>A SKCM-US 14 89154685 89154685 single base substitution C T 3_prime_UTR_variant SKCM-US 14 89154685 89154685 single base substitution C T missense_variant R853K 2558G>A SKCM-US 14 89154685 89154685 single base substitution C T missense_variant R891K 2672G>A SKCM-US 14 89154722 89154722 single base substitution A C intron_variant SKCM-US 14 89154722 89154722 single base substitution A C missense_variant F879V 2635T>G SKCM-US 14 89154729 89154729 single base substitution C T intron_variant SKCM-US 14 89154729 89154729 single base substitution C T synonymous_variant E876E 2628G>A SKCM-US 14 89163205 89163205 single base substitution G A 3_prime_UTR_variant SKCM-US 14 89163205 89163205 single base substitution G A missense_variant A777V 2330C>T SKCM-US 14 89168884 89168884 single base substitution C T 3_prime_UTR_variant SKCM-US 14 89168884 89168884 single base substitution C T missense_variant R715Q 2144G>A SKCM-US 14 89171280 89171280 single base substitution C T 3_prime_UTR_variant SKCM-US 14 89171280 89171280 single base substitution C T missense_variant E659K 1975G>A SKCM-US 14 89172638 89172638 single base substitution C T exon_variant SKCM-US 14 89172638 89172638 single base substitution C T missense_variant R597K 1790G>A SKCM-US 14 89178744 89178744 single base substitution C T exon_variant SKCM-US 14 89178744 89178744 single base substitution C T missense_variant G510R 1528G>A SKCM-US 14 89178746 89178746 single base substitution T A exon_variant SKCM-US 14 89178746 89178746 single base substitution T A missense_variant N509I 1526A>T SKCM-US 14 89181355 89181355 single base substitution C T exon_variant SKCM-US 14 89181355 89181355 single base substitution C T missense_variant D458N 1372G>A SKCM-US 14 89181462 89181462 single base substitution T A exon_variant SKCM-US 14 89181462 89181462 single base substitution T A missense_variant Y422F 1265A>T SKCM-US 14 89202718 89202718 single base substitution G A missense_variant R347C 1039C>T SKCM-US 14 89202745 89202745 single base substitution G A missense_variant P338S 1012C>T SKCM-US 14 89202882 89202882 single base substitution C T missense_variant R292Q 875G>A SKCM-US 14 89206850 89206850 single base substitution G A stop_gained Q198* 592C>T SKCM-US 14 89206879 89206879 single base substitution C T missense_variant R188Q 563G>A SKCM-US 14 89220907 89220907 single base substitution C T synonymous_variant K102K 306G>A STAD-US 14 89075670 89075670 single base substitution A G downstream_gene_variant STAD-US 14 89076102 89076102 single base substitution C T downstream_gene_variant STAD-US 14 89082574 89082574 insertion of <=200bp - T 3_prime_UTR_variant STAD-US 14 89082574 89082574 insertion of <=200bp - T downstream_gene_variant STAD-US 14 89082574 89082574 insertion of <=200bp - T exon_variant STAD-US 14 89082574 89082574 insertion of <=200bp - T frameshift_variant R1891K? STAD-US 14 89082574 89082574 insertion of <=200bp - T frameshift_variant R1929K? STAD-US 14 89082574 89082574 insertion of <=200bp - T frameshift_variant R1937K? STAD-US 14 89087177 89087177 single base substitution C A 3_prime_UTR_variant STAD-US 14 89087177 89087177 single base substitution C A downstream_gene_variant STAD-US 14 89087177 89087177 single base substitution C A stop_gained E1720* 5158G>T STAD-US 14 89087177 89087177 single base substitution C A stop_gained E1758* 5272G>T STAD-US 14 89087177 89087177 single base substitution C A stop_gained E1766* 5296G>T STAD-US 14 89087177 89087177 single base substitution C A stop_gained E206* 616G>T STAD-US 14 89087177 89087177 single base substitution C A upstream_gene_variant STAD-US 14 89088957 89088957 single base substitution G A 3_prime_UTR_variant STAD-US 14 89088957 89088957 single base substitution G A intron_variant STAD-US 14 89088957 89088957 single base substitution G A synonymous_variant C109C 327C>T STAD-US 14 89088957 89088957 single base substitution G A synonymous_variant C1622C 4866C>T STAD-US 14 89088957 89088957 single base substitution G A synonymous_variant C1660C 4980C>T STAD-US 14 89088957 89088957 single base substitution G A synonymous_variant C1668C 5004C>T STAD-US 14 89088957 89088957 single base substitution G A upstream_gene_variant STAD-US 14 89091345 89091345 single base substitution C T 3_prime_UTR_variant STAD-US 14 89091345 89091345 single base substitution C T downstream_gene_variant STAD-US 14 89091345 89091345 single base substitution C T exon_variant STAD-US 14 89091345 89091345 single base substitution C T missense_variant G1577R 4729G>A STAD-US 14 89091345 89091345 single base substitution C T missense_variant G1615R 4843G>A STAD-US 14 89091345 89091345 single base substitution C T missense_variant G1623R 4867G>A STAD-US 14 89091345 89091345 single base substitution C T missense_variant G64R 190G>A STAD-US 14 89091363 89091363 single base substitution A G 3_prime_UTR_variant STAD-US 14 89091363 89091363 single base substitution A G downstream_gene_variant STAD-US 14 89091363 89091363 single base substitution A G exon_variant STAD-US 14 89091363 89091363 single base substitution A G missense_variant Y1571H 4711T>C STAD-US 14 89091363 89091363 single base substitution A G missense_variant Y1609H 4825T>C STAD-US 14 89091363 89091363 single base substitution A G missense_variant Y1617H 4849T>C STAD-US 14 89091363 89091363 single base substitution A G missense_variant Y58H 172T>C STAD-US 14 89123818 89123818 single base substitution A G 3_prime_UTR_variant STAD-US 14 89123818 89123818 single base substitution A G synonymous_variant N1264N 3792T>C STAD-US 14 89123818 89123818 single base substitution A G synonymous_variant N1302N 3906T>C STAD-US 14 89123848 89123848 single base substitution T C splice_acceptor_variant STAD-US 14 89124530 89124530 single base substitution C G splice_donor_variant STAD-US 14 89130844 89130844 single base substitution A G 3_prime_UTR_variant STAD-US 14 89130844 89130844 single base substitution A G exon_variant STAD-US 14 89130844 89130844 single base substitution A G synonymous_variant D1096D 3288T>C STAD-US 14 89130844 89130844 single base substitution A G synonymous_variant D1134D 3402T>C STAD-US 14 89153595 89153595 single base substitution G A 3_prime_UTR_variant STAD-US 14 89153595 89153595 single base substitution G A missense_variant A902V 2705C>T STAD-US 14 89153595 89153595 single base substitution G A missense_variant A940V 2819C>T STAD-US 14 89154769 89154769 deletion of <=200bp T - frameshift_variant N863 STAD-US 14 89154769 89154769 deletion of <=200bp T - intron_variant STAD-US 14 89154773 89154773 single base substitution T C intron_variant STAD-US 14 89154773 89154773 single base substitution T C missense_variant K862E 2584A>G STAD-US 14 89163261 89163261 single base substitution T C 3_prime_UTR_variant STAD-US 14 89163261 89163261 single base substitution T C synonymous_variant T758T 2274A>G STAD-US 14 89168805 89168805 single base substitution G C 3_prime_UTR_variant STAD-US 14 89168805 89168805 single base substitution G C stop_gained Y741* 2223C>G STAD-US 14 89171305 89171305 single base substitution T C 3_prime_UTR_variant STAD-US 14 89171305 89171305 single base substitution T C synonymous_variant L650L 1950A>G STAD-US 14 89181530 89181530 single base substitution C T synonymous_variant T399T 1197G>A STAD-US 14 89181530 89181530 single base substitution C T upstream_gene_variant STAD-US 14 89202717 89202717 single base substitution C T missense_variant R347H 1040G>A STAD-US 14 89206753 89206753 single base substitution C T missense_variant R230Q 689G>A STAD-US 14 89206880 89206880 single base substitution G A stop_gained R188* 562C>T UCEC-US 14 89075730 89075730 single base substitution T C downstream_gene_variant UCEC-US 14 89082504 89082504 single base substitution G A 3_prime_UTR_variant UCEC-US 14 89082504 89082504 single base substitution G A downstream_gene_variant UCEC-US 14 89082504 89082504 single base substitution G A exon_variant UCEC-US 14 89082504 89082504 single base substitution G A missense_variant A1914V 5741C>T UCEC-US 14 89082504 89082504 single base substitution G A missense_variant A1952V 5855C>T UCEC-US 14 89082504 89082504 single base substitution G A missense_variant A1960V 5879C>T UCEC-US 14 89082509 89082511 deletion of <=200bp AAC - 3_prime_UTR_variant UCEC-US 14 89082509 89082511 deletion of <=200bp AAC - downstream_gene_variant UCEC-US 14 89082509 89082511 deletion of <=200bp AAC - exon_variant UCEC-US 14 89082509 89082511 deletion of <=200bp AAC - inframe_deletion V1912 UCEC-US 14 89082509 89082511 deletion of <=200bp AAC - inframe_deletion V1950 UCEC-US 14 89082509 89082511 deletion of <=200bp AAC - inframe_deletion V1958 UCEC-US 14 89083107 89083107 single base substitution A G 3_prime_UTR_variant UCEC-US 14 89083107 89083107 single base substitution A G downstream_gene_variant UCEC-US 14 89083107 89083107 single base substitution A G exon_variant UCEC-US 14 89083107 89083107 single base substitution A G missense_variant M1874T 5621T>C UCEC-US 14 89083107 89083107 single base substitution A G missense_variant M1912T 5735T>C UCEC-US 14 89083107 89083107 single base substitution A G missense_variant M1920T 5759T>C UCEC-US 14 89083113 89083113 single base substitution A G 3_prime_UTR_variant UCEC-US 14 89083113 89083113 single base substitution A G downstream_gene_variant UCEC-US 14 89083113 89083113 single base substitution A G exon_variant UCEC-US 14 89083113 89083113 single base substitution A G missense_variant F1872S 5615T>C UCEC-US 14 89083113 89083113 single base substitution A G missense_variant F1910S 5729T>C UCEC-US 14 89083113 89083113 single base substitution A G missense_variant F1918S 5753T>C UCEC-US 14 89083152 89083152 single base substitution A G 3_prime_UTR_variant UCEC-US 14 89083152 89083152 single base substitution A G downstream_gene_variant UCEC-US 14 89083152 89083152 single base substitution A G exon_variant UCEC-US 14 89083152 89083152 single base substitution A G missense_variant V1859A 5576T>C UCEC-US 14 89083152 89083152 single base substitution A G missense_variant V1897A 5690T>C UCEC-US 14 89083152 89083152 single base substitution A G missense_variant V1905A 5714T>C UCEC-US 14 89083213 89083215 deletion of <=200bp CTC - 3_prime_UTR_variant UCEC-US 14 89083213 89083215 deletion of <=200bp CTC - disruptive_inframe_deletion GD1838D UCEC-US 14 89083213 89083215 deletion of <=200bp CTC - disruptive_inframe_deletion GD1876D UCEC-US 14 89083213 89083215 deletion of <=200bp CTC - disruptive_inframe_deletion GD1884D UCEC-US 14 89083213 89083215 deletion of <=200bp CTC - downstream_gene_variant UCEC-US 14 89083213 89083215 deletion of <=200bp CTC - exon_variant UCEC-US 14 89084596 89084596 single base substitution C A 3_prime_UTR_variant UCEC-US 14 89084596 89084596 single base substitution C A downstream_gene_variant UCEC-US 14 89084596 89084596 single base substitution C A exon_variant UCEC-US 14 89084596 89084596 single base substitution C A missense_variant R1827I 5480G>T UCEC-US 14 89084596 89084596 single base substitution C A missense_variant R1865I 5594G>T UCEC-US 14 89084596 89084596 single base substitution C A missense_variant R1873I 5618G>T UCEC-US 14 89087152 89087152 single base substitution G T 3_prime_UTR_variant UCEC-US 14 89087152 89087152 single base substitution G T downstream_gene_variant UCEC-US 14 89087152 89087152 single base substitution G T missense_variant S1728Y 5183C>A UCEC-US 14 89087152 89087152 single base substitution G T missense_variant S1766Y 5297C>A UCEC-US 14 89087152 89087152 single base substitution G T missense_variant S1774Y 5321C>A UCEC-US 14 89087152 89087152 single base substitution G T missense_variant S214Y 641C>A UCEC-US 14 89087152 89087152 single base substitution G T upstream_gene_variant UCEC-US 14 89093199 89093199 single base substitution C T 3_prime_UTR_variant UCEC-US 14 89093199 89093199 single base substitution C T downstream_gene_variant UCEC-US 14 89093199 89093199 single base substitution C T exon_variant UCEC-US 14 89093199 89093199 single base substitution C T missense_variant A1529T 4585G>A UCEC-US 14 89093199 89093199 single base substitution C T missense_variant A1567T 4699G>A UCEC-US 14 89093199 89093199 single base substitution C T missense_variant A1575T 4723G>A UCEC-US 14 89093199 89093199 single base substitution C T missense_variant A16T 46G>A UCEC-US 14 89093354 89093354 single base substitution C T 3_prime_UTR_variant UCEC-US 14 89093354 89093354 single base substitution C T downstream_gene_variant UCEC-US 14 89093354 89093354 single base substitution C T missense_variant R1477H 4430G>A UCEC-US 14 89093354 89093354 single base substitution C T missense_variant R1515H 4544G>A UCEC-US 14 89093354 89093354 single base substitution C T missense_variant R1523H 4568G>A UCEC-US 14 89093354 89093354 single base substitution C T upstream_gene_variant UCEC-US 14 89110800 89110800 single base substitution C T 3_prime_UTR_variant UCEC-US 14 89110800 89110800 single base substitution C T exon_variant UCEC-US 14 89110800 89110800 single base substitution C T missense_variant G1316S 3946G>A UCEC-US 14 89110800 89110800 single base substitution C T missense_variant G1354S 4060G>A UCEC-US 14 89110800 89110800 single base substitution C T missense_variant G1362S 4084G>A UCEC-US 14 89123784 89123784 single base substitution T G 3_prime_UTR_variant UCEC-US 14 89123784 89123784 single base substitution T G missense_variant N1276H 3826A>C UCEC-US 14 89123784 89123784 single base substitution T G missense_variant N1314H 3940A>C UCEC-US 14 89124599 89124599 single base substitution A C 3_prime_UTR_variant UCEC-US 14 89124599 89124599 single base substitution A C missense_variant M1232R 3695T>G UCEC-US 14 89124599 89124599 single base substitution A C missense_variant M1270R 3809T>G UCEC-US 14 89124730 89124730 single base substitution C A splice_region_variant UCEC-US 14 89130878 89130878 single base substitution C A 3_prime_UTR_variant UCEC-US 14 89130878 89130878 single base substitution C A exon_variant UCEC-US 14 89130878 89130878 single base substitution C A missense_variant G1085V 3254G>T UCEC-US 14 89130878 89130878 single base substitution C A missense_variant G1123V 3368G>T UCEC-US 14 89148262 89148262 single base substitution A G 3_prime_UTR_variant UCEC-US 14 89148262 89148262 single base substitution A G synonymous_variant C1032C 3096T>C UCEC-US 14 89148262 89148262 single base substitution A G synonymous_variant C994C 2982T>C UCEC-US 14 89148307 89148307 single base substitution G A 3_prime_UTR_variant UCEC-US 14 89148307 89148307 single base substitution G A synonymous_variant S1017S 3051C>T UCEC-US 14 89148307 89148307 single base substitution G A synonymous_variant S979S 2937C>T UCEC-US 14 89153590 89153590 single base substitution T G 3_prime_UTR_variant UCEC-US 14 89153590 89153590 single base substitution T G missense_variant K904Q 2710A>C UCEC-US 14 89153590 89153590 single base substitution T G missense_variant K942Q 2824A>C UCEC-US 14 89154678 89154678 single base substitution G T 3_prime_UTR_variant UCEC-US 14 89154678 89154678 single base substitution G T synonymous_variant I855I 2565C>A UCEC-US 14 89154678 89154678 single base substitution G T synonymous_variant I893I 2679C>A UCEC-US 14 89154729 89154729 single base substitution C A intron_variant UCEC-US 14 89154729 89154729 single base substitution C A missense_variant E876D 2628G>T UCEC-US 14 89154750 89154750 single base substitution T A intron_variant UCEC-US 14 89154750 89154750 single base substitution T A synonymous_variant A869A 2607A>T UCEC-US 14 89160660 89160660 single base substitution G A 3_prime_UTR_variant UCEC-US 14 89160660 89160660 single base substitution G A missense_variant R844C 2530C>T UCEC-US 14 89161745 89161745 single base substitution G A 3_prime_UTR_variant UCEC-US 14 89161745 89161745 single base substitution G A missense_variant L800F 2398C>T UCEC-US 14 89171222 89171222 single base substitution C T 3_prime_UTR_variant UCEC-US 14 89171222 89171222 single base substitution C T missense_variant R678Q 2033G>A UCEC-US 14 89171223 89171223 single base substitution G A 3_prime_UTR_variant UCEC-US 14 89171223 89171223 single base substitution G A stop_gained R678* 2032C>T UCEC-US 14 89171831 89171831 single base substitution G A 3_prime_UTR_variant UCEC-US 14 89171831 89171831 single base substitution G A stop_gained R643* 1927C>T UCEC-US 14 89172631 89172631 single base substitution C A exon_variant UCEC-US 14 89172631 89172631 single base substitution C A synonymous_variant L599L 1797G>T UCEC-US 14 89181303 89181303 single base substitution C A exon_variant UCEC-US 14 89181303 89181303 single base substitution C A missense_variant R475I 1424G>T UCEC-US 14 89181321 89181321 single base substitution T G exon_variant UCEC-US 14 89181321 89181321 single base substitution T G missense_variant N469T 1406A>C UCEC-US 14 89181408 89181408 single base substitution C T exon_variant UCEC-US 14 89181408 89181408 single base substitution C T missense_variant R440H 1319G>A UCEC-US 14 89202903 89202903 single base substitution G T missense_variant S285Y 854C>A UCEC-US 14 89206739 89206739 single base substitution C T missense_variant A235T 703G>A UCEC-US 14 89210416 89210416 single base substitution T C missense_variant D159G 476A>G

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CHC892T COSM4798307 c.3076G>A p.D1026N Substitution - Missense 14:88681938-88681938 - TCGA-06-5858-01 COSM3401503 c.2531G>A p.R844H Substitution - Missense 14:88694315-88694315 - TCGA-D1-A17Q-01 COSM958532 c.2824A>C p.K942Q Substitution - Missense 14:88687246-88687246 - TCGA-AA-3510-01 COSM1371451 c.301T>G p.L101V Substitution - Missense 14:88754568-88754568 - RKO COSM2250614 c.1678A>G p.I560V Substitution - Missense 14:88706406-88706406 - T578 COSM4680920 c.1302T>G p.I434M Substitution - Missense 14:88715081-88715081 - BN41T COSM1608037 c.4586T>G p.F1529C Substitution - Missense 14:88626992-88626992 - TCGA-HW-8322-01 COSM3968953 c.2487T>A p.P829P Substitution - coding silent 14:88694359-88694359 - TCGA-33-4586-01 COSM699155 c.2332G>T p.V778F Substitution - Missense 14:88696859-88696859 - WSU-HN8 COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - TCGA-AP-A056-01 COSM958534 c.2679C>A p.I893I Substitution - coding silent 14:88688334-88688334 - BD236T COSM5519275 c.4615T>G p.S1539A Substitution - Missense 14:88626963-88626963 - CSCC-44-T COSM4569714 c.1969T>G p.C657G Substitution - Missense 14:88704942-88704942 - BD72T COSM5513053 c.4666_4668delCTT p.L1556delL Deletion - In frame 14:88626910-88626912 - TCGA-HU-A4G9-01 COSM4052828 c.3878-2A>G p.? Unknown 14:88657504-88657504 - BD57T COSM4772714 c.2743-7delT p.? Unknown 14:88687334-88687334 - TCGA-AZ-4615-01 COSM5139660 c.5291delA p.N1764fs*8 Deletion - Frameshift 14:88620838-88620838 - CHC892T COSM4796789 c.1229C>T p.A410V Substitution - Missense 14:88715154-88715154 - TCGA-AG-A002-01 COSM260682 c.4862G>A p.R1621Q Substitution - Missense 14:88625006-88625006 - TCGA-BS-A0UV-01 COSM958548 c.1927C>T p.R643* Substitution - Nonsense 14:88705487-88705487 - Pat_66_A COSM5848653 c.5846G>A p.R1949Q Substitution - Missense 14:88616193-88616193 - TCGA-AG-A002-01 COSM260681 c.5053G>A p.E1685K Substitution - Missense 14:88621262-88621262 - TCGA-BR-4362-01 COSM4052843 c.1040G>A p.R347H Substitution - Missense 14:88736373-88736373 - TCGA-BP-4795-01 COSM1493354 c.2838G>A p.L946L Substitution - coding silent 14:88687232-88687232 - TCGA-AP-A0LM-01 COSM958520 c.3940A>C p.N1314H Substitution - Missense 14:88657440-88657440 - ESO-0129 COSM1251168 c.4229T>C p.V1410A Substitution - Missense 14:88642901-88642901 - TCGA-AG-A002-01 COSM260683 c.2340C>T p.F780F Substitution - coding silent 14:88696851-88696851 - BK0023 COSM4186399 c.2491A>G p.K831E Substitution - Missense 14:88694355-88694355 - CHC892T COSM4797326 c.1050G>A p.R350R Substitution - coding silent 14:88726678-88726678 - TCGA-BS-A0UF-01 COSM958558 c.854C>A p.S285Y Substitution - Missense 14:88736559-88736559 - CRC-06T COSM2250533 c.4875C>T p.I1625I Substitution - coding silent 14:88624993-88624993 - BD239T COSM5497251 c.5461A>C p.N1821H Substitution - Missense 14:88618727-88618727 - HCC2998 COSM958511 c.5321C>A p.S1774Y Substitution - Missense 14:88620808-88620808 - CSCC-27-T COSM4535421 c.218G>A p.R73Q Substitution - Missense 14:88754651-88754651 - OSCC-GB_01240111 COSM5954118 c.5796+8T>C p.? Unknown 14:88616718-88616718 - LOVO COSM2250549 c.4273A>G p.I1425V Substitution - Missense 14:88638872-88638872 - TCGA-CZ-4857-01 COSM3361253 c.3532G>T p.V1178L Substitution - Missense 14:88661797-88661797 - TCGA-FS-A1ZQ-06 COSM3498555 c.4366C>T p.P1456S Substitution - Missense 14:88627811-88627811 - PTC-28C COSM4148290 c.582G>C p.T194T Substitution - coding silent 14:88740516-88740516 - TCGA-CM-5341-01 COSM3690230 c.3023C>A p.P1008H Substitution - Missense 14:88681991-88681991 - S02285 COSM5684553 c.1408G>T p.D470Y Substitution - Missense 14:88714975-88714975 - CRC-02T COSM5454314 c.2268G>A p.W756* Substitution - Nonsense 14:88696923-88696923 - ESO-1163 COSM1251169 c.5364C>G p.I1788M Substitution - Missense 14:88620765-88620765 - TCGA-EK-A2RB-01 COSM4820080 c.5647C>A p.L1883I Substitution - Missense 14:88616875-88616875 - U373 COSM2250608 c.1914G>T p.Q638H Substitution - Missense 14:88705500-88705500 - TCGA-BR-4361-01 COSM2250600 c.2274A>G p.T758T Substitution - coding silent 14:88696917-88696917 - HCC2998 COSM2250628 c.1137C>T p.I379I Substitution - coding silent 14:88726591-88726591 - AOCS-095-1-4 COSM3943906 c.3933A>G p.L1311L Substitution - coding silent 14:88657447-88657447 - TCGA-AX-A05Z-01 COSM958562 c.476A>G p.D159G Substitution - Missense 14:88744072-88744072 - 202_T COSM3956272 c.567T>A p.G189G Substitution - coding silent 14:88740531-88740531 - 2296357 COSM4766139 c.1619G>A p.G540E Substitution - Missense 14:88712309-88712309 - HCC2998 COSM2250591 c.2521A>C p.K841Q Substitution - Missense 14:88694325-88694325 - TCGA-F1-A448-01 COSM4052820 c.5004C>T p.C1668C Substitution - coding silent 14:88622613-88622613 - MO_1074 COSM5547134 c.2703_2704delGC p.H902fs*1 Deletion - Frameshift 14:88688309-88688310 - TCGA-AP-A051-01 COSM958530 c.3051C>T p.S1017S Substitution - coding silent 14:88681963-88681963 - CSCC-38-T COSM4539599 c.2707G>A p.D903N Substitution - Missense 14:88688306-88688306 - TCGA-D8-A1XK-01 COSM5224657 c.3829delA p.R1277fs*43 Deletion - Frameshift 14:88658235-88658235 - TP_2020 COSM5570791 c.47T>G p.V16G Substitution - Missense 14:88792457-88792457 - S02285 COSM2250624 c.1220G>A p.R407K Substitution - Missense 14:88715163-88715163 - CRC-11T COSM5460514 c.3877+4C>T p.? Unknown 14:88658183-88658183 - TCGA-18-3409-01 COSM699152 c.1350C>T p.S450S Substitution - coding silent 14:88715033-88715033 - SNU-C4 COSM4652561 c.4464T>C p.T1488T Substitution - coding silent 14:88627713-88627713 - TCGA-D3-A5GO-06 COSM3498586 c.1012C>T p.P338S Substitution - Missense 14:88736401-88736401 - EV006-R4 COSM4410912 c.5611A>T p.I1871F Substitution - Missense 14:88618259-88618259 - EGC15 COSM5054124 c.4898+1G>A p.? Unknown 14:88624969-88624969 - TCGA-AZ-4315-01 COSM1371450 c.912A>C p.E304D Substitution - Missense 14:88736501-88736501 - TCGA-EE-A2GO-06 COSM2250633 c.1039C>T p.R347C Substitution - Missense 14:88736374-88736374 - 587228 COSM1205266 c.875G>A p.R292Q Substitution - Missense 14:88736538-88736538 - WSU-HN30 COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - TCGA-D3-A3MU-06 COSM3498569 c.2635T>G p.F879V Substitution - Missense 14:88688378-88688378 - TCGA-24-1431-01 COSM86632 c.3498G>A p.E1166E Substitution - coding silent 14:88663031-88663031 - RK035_C01 COSM1629423 c.2440G>A p.G814R Substitution - Missense 14:88694406-88694406 - BD96T COSM5520620 c.358-5A>G p.? Unknown 14:88746288-88746288 - TCGA-EE-A2MF-06 COSM4893336 c.3063C>T p.T1021T Substitution - coding silent 14:88681951-88681951 - 2492713 COSM260681 c.5053G>A p.E1685K Substitution - Missense 14:88621262-88621262 - TCGA-06-0644-01 COSM3401499 c.5607C>T p.A1869A Substitution - coding silent 14:88618263-88618263 - TCGA-AP-A054-01 COSM958501 c.5759T>C p.M1920T Substitution - Missense 14:88616763-88616763 - YUPAER COSM5382792 c.2737G>A p.E913K Substitution - Missense 14:88688276-88688276 - TCGA-AP-A0LM-01 COSM958514 c.4568G>A p.R1523H Substitution - Missense 14:88627010-88627010 - TCGA-BS-A0UF-01 COSM958544 c.2033G>A p.R678Q Substitution - Missense 14:88704878-88704878 - PD7192a COSM3769808 c.1445-1G>A p.? Unknown 14:88712484-88712484 - LUAD-B00915 COSM332654 c.4228G>A p.V1410I Substitution - Missense 14:88642902-88642902 - 587376 COSM958552 c.1424G>T p.R475I Substitution - Missense 14:88714959-88714959 - TCGA-AZ-4315-01 COSM1371445 c.3350G>A p.R1117Q Substitution - Missense 14:88664552-88664552 - TCGA-AX-A0J0-01 COSM958526 c.3368G>T p.G1123V Substitution - Missense 14:88664534-88664534 - TCGA-AP-A0LM-01 COSM958536 c.2628G>T p.E876D Substitution - Missense 14:88688385-88688385 - PT36 COSM5916349 c.2438G>A p.R813K Substitution - Missense 14:88695361-88695361 - CHEWS020 COSM3968952 c.2584A>G p.K862E Substitution - Missense 14:88688429-88688429 - 10-276 COSM3736745 c.1259G>A p.G420E Substitution - Missense 14:88715124-88715124 - TCGA-BR-8680-01 COSM4052818 c.5296G>T p.E1766* Substitution - Nonsense 14:88620833-88620833 - 75 COSM5012804 c.1715C>A p.S572* Substitution - Nonsense 14:88706369-88706369 - TCGA-B6-A0IK-01 COSM433455 c.368C>A p.S123* Substitution - Nonsense 14:88746273-88746273 - LIM2099 COSM4641064 c.1967A>G p.Q656R Substitution - Missense 14:88704944-88704944 - LUAD-RT-S01477 COSM377468 c.4455C>T p.F1485F Substitution - coding silent 14:88627722-88627722 - PT44 COSM5926884 c.5666G>A p.G1889E Substitution - Missense 14:88616856-88616856 - GCT25 COSM5749266 c.1496C>T p.S499L Substitution - Missense 14:88712432-88712432 - T3225 COSM4680910 c.4813G>A p.V1605M Substitution - Missense 14:88625055-88625055 - TCGA-FS-A1Z3-06 COSM3498559 c.3946C>T p.R1316C Substitution - Missense 14:88657434-88657434 - YUROL COSM5382798 c.1665G>A p.K555K Substitution - coding silent 14:88706419-88706419 - C99 COSM4611325 c.4454delT p.F1485fs*13 Deletion - Frameshift 14:88627723-88627723 - 587222 COSM1205267 c.1391G>T p.R464I Substitution - Missense 14:88714992-88714992 - TCGA-BR-4361-01 COSM4052830 c.3877+1G>C p.? Unknown 14:88658186-88658186 - CSCC-18-T COSM4545981 c.3901G>A p.E1301K Substitution - Missense 14:88657479-88657479 - TCGA-QB-A6FS-06 COSM3886470 c.1975G>A p.E659K Substitution - Missense 14:88704936-88704936 - sysucc-1397T COSM5473582 c.3775A>G p.T1259A Substitution - Missense 14:88658289-88658289 - TCGA-CM-6162-01 COSM1371448 c.1657+1G>A p.? Unknown 14:88712270-88712270 - TCGA-26-5134-01 COSM3401505 c.2223C>T p.Y741Y Substitution - coding silent 14:88702461-88702461 - CSCC-10-T COSM4491784 c.3863C>T p.S1288F Substitution - Missense 14:88658201-88658201 - 824_T COSM3956270 c.2471T>G p.M824R Substitution - Missense 14:88694375-88694375 - PT49 COSM5936054 c.1445-5T>A p.? Unknown 14:88712488-88712488 - TCGA-EI-6917-01 COSM1608036 c.4993C>T p.R1665C Substitution - Missense 14:88622624-88622624 - CHC892T COSM4796789 c.1229C>T p.A410V Substitution - Missense 14:88715154-88715154 - T2944 COSM4680914 c.3456delT p.F1152fs*16 Deletion - Frameshift 14:88663073-88663073 - CSCC-27-T COSM4493154 c.4100C>T p.P1367L Substitution - Missense 14:88644440-88644440 - 2492714 COSM260681 c.5053G>A p.E1685K Substitution - Missense 14:88621262-88621262 - TCGA-22-5482-01 COSM699150 c.997G>T p.V333F Substitution - Missense 14:88736416-88736416 - J52_T COSM3956263 c.4028+9C>T p.? Unknown 14:88646938-88646938 - 1N21-VS-1T21 COSM4972973 c.4705C>T p.R1569W Substitution - Missense 14:88626873-88626873 - ESCC-112T COSM3936649 c.1237G>A p.E413K Substitution - Missense 14:88715146-88715146 - LP6005690-DNA_E03 COSM5952728 c.1103C>T p.P368L Substitution - Missense 14:88726625-88726625 - TCGA-AA-3663-01 COSM1371447 c.1659G>A p.G553G Substitution - coding silent 14:88706425-88706425 - TCGA-B5-A11N-01 COSM958511 c.5321C>A p.S1774Y Substitution - Missense 14:88620808-88620808 - J88_T COSM3956264 c.3498+5G>A p.? Unknown 14:88663026-88663026 - TCGA-AA-3715-01 COSM269095 c.3947G>A p.R1316H Substitution - Missense 14:88657433-88657433 - HCC70T COSM1608038 c.1662C>A p.A554A Substitution - coding silent 14:88706422-88706422 - SNUH_G73_S1 COSM4415047 c.2011C>G p.R671G Substitution - Missense 14:88704900-88704900 - TCGA-AA-3811-01 COSM270652 c.4907_4909delAAG p.E1636delE Deletion - In frame 14:88622708-88622710 - YUGATOR COSM5382800 c.1490G>A p.W497* Substitution - Nonsense 14:88712438-88712438 - LP6007512-DNA_A01 COSM5033223 c.2982+10A>T p.? Unknown 14:88685005-88685005 - 8033414 COSM3386722 c.803C>G p.P268R Substitution - Missense 14:88738923-88738923 - TCGA-AA-A010-01 COSM280787 c.3762T>G p.V1254V Substitution - coding silent 14:88658302-88658302 - T1844 COSM4680916 c.3146C>T p.S1049F Substitution - Missense 14:88665468-88665468 - 446 COSM4434956 c.1618G>T p.G540* Substitution - Nonsense 14:88712310-88712310 - UM-SCC-4 COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - RK308_C01 COSM3744466 c.2943A>G p.L981L Substitution - coding silent 14:88685054-88685054 - TCGA-B5-A11N-01 COSM958546 c.2032C>T p.R678* Substitution - Nonsense 14:88704879-88704879 - TCGA-CJ-4920-01 COSM470321 c.1049G>C p.R350T Substitution - Missense 14:88736364-88736364 - TCGA-G3-A25W-01 COSM4927157 c.3852C>A p.S1284S Substitution - coding silent 14:88658212-88658212 - STC252 COSM5054128 c.1503A>G p.T501T Substitution - coding silent 14:88712425-88712425 - 2497773 COSM5750428 c.688C>T p.R230* Substitution - Nonsense 14:88740410-88740410 - C0053T COSM4150861 c.5803C>T p.H1935Y Substitution - Missense 14:88616236-88616236 - TCGA-66-2754-01 COSM699160 c.5248T>C p.C1750R Substitution - Missense 14:88620881-88620881 - TCGA-D1-A17Q-01 COSM958503 c.5753T>C p.F1918S Substitution - Missense 14:88616769-88616769 - 2492711 COSM260681 c.5053G>A p.E1685K Substitution - Missense 14:88621262-88621262 - 2293753 COSM4606744 c.4688G>A p.S1563N Substitution - Missense 14:88626890-88626890 - Pat_28_B COSM5848655 c.5651G>A p.G1884E Substitution - Missense 14:88616871-88616871 - TCGA-AP-A0LD-01 COSM958505 c.5714T>C p.V1905A Substitution - Missense 14:88616808-88616808 - TCGA-AZ-4615-01 COSM3754146 c.132C>T p.G44G Substitution - coding silent 14:88792372-88792372 - PT08_2 COSM5893765 c.4899G>A p.P1633P Substitution - coding silent 14:88622718-88622718 - TCGA-HE-7130-01 COSM3987813 c.2416G>A p.G806R Substitution - Missense 14:88695383-88695383 - STC291 COSM5054126 c.4222C>T p.H1408Y Substitution - Missense 14:88642908-88642908 - HCC70 COSM1608038 c.1662C>A p.A554A Substitution - coding silent 14:88706422-88706422 - T2769 COSM4680924 c.217C>T p.R73* Substitution - Nonsense 14:88754652-88754652 - TCGA-BR-6452-01 COSM4052846 c.562C>T p.R188* Substitution - Nonsense 14:88740536-88740536 - 46M COSM5587718 c.4524G>T p.W1508C Substitution - Missense 14:88627653-88627653 - TCGA-B5-A0JY-01 COSM958552 c.1424G>T p.R475I Substitution - Missense 14:88714959-88714959 - BN49 COSM3706421 c.5539-2A>G p.? Unknown 14:88618333-88618333 - sysucc-1317T COSM5448699 c.3124+3A>G p.? Unknown 14:88681887-88681887 - TCGA-AA-3510-01 COSM1371444 c.3985G>T p.E1329* Substitution - Nonsense 14:88657395-88657395 - TCGA-AD-6895-01 COSM1371446 c.3154G>A p.G1052S Substitution - Missense 14:88665460-88665460 - PD13756a COSM5801247 c.5202+6_5202+7insGTA p.? Unknown 14:88621106-88621107 - ESCC_164 COSM5648194 c.4043G>T p.R1348M Substitution - Missense 14:88644497-88644497 - PD13752a COSM5777008 c.162G>T p.Q54H Substitution - Missense 14:88792342-88792342 - TCGA-EE-A3J4-06 COSM3886468 c.2953A>G p.K985E Substitution - Missense 14:88685044-88685044 - SJDES011-R COSM4578050 c.568delG p.V190fs*14 Deletion - Frameshift 14:88740530-88740530 - TCGA-B0-5701-01 COSM3361255 c.2110T>A p.Y704N Substitution - Missense 14:88702574-88702574 - CSCC-32-T COSM4459012 c.1108C>T p.R370C Substitution - Missense 14:88726620-88726620 - TCGA-EJ-5518-01 COSM1128177 c.2213T>C p.L738S Substitution - Missense 14:88702471-88702471 - BN49T COSM3706421 c.5539-2A>G p.? Unknown 14:88618333-88618333 - 587338 COSM1205268 c.4817C>T p.A1606V Substitution - Missense 14:88625051-88625051 - UM-SCC-17B COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - CHC1079T COSM4791076 c.1056G>T p.W352C Substitution - Missense 14:88726672-88726672 - TCGA-BR-6452-01 COSM4052826 c.3906T>C p.N1302N Substitution - coding silent 14:88657474-88657474 - TCGA-GL-A4EM-01 COSM3987811 c.4265A>C p.N1422T Substitution - Missense 14:88638880-88638880 - TCGA-B8-5549-01 COSM470318 c.4736G>A p.G1579D Substitution - Missense 14:88626842-88626842 - TCGA-EE-A29E-06 COSM3498583 c.1265A>T p.Y422F Substitution - Missense 14:88715118-88715118 - YUKAT COSM5382796 c.1986A>G p.K662K Substitution - coding silent 14:88704925-88704925 - CN-AML-NR-08-Dx COSM5426025 c.5094C>T p.N1698N Substitution - coding silent 14:88621221-88621221 - TCGA-AG-3592-01 COSM3420081 c.2072G>T p.R691L Substitution - Missense 14:88702612-88702612 - UMC11 COSM2250651 c.374G>C p.G125A Substitution - Missense 14:88746267-88746267 - HN_00076 COSM122833 c.2182G>T p.D728Y Substitution - Missense 14:88702502-88702502 - T1743 COSM260680 c.5845C>T p.R1949* Substitution - Nonsense 14:88616194-88616194 - TCGA-EW-A1OV-01 COSM1477816 c.2808C>A p.L936L Substitution - coding silent 14:88687262-88687262 - CHC1079T COSM4791076 c.1056G>T p.W352C Substitution - Missense 14:88726672-88726672 - CSCC-4-T COSM4551851 c.5428G>A p.D1810N Substitution - Missense 14:88618760-88618760 - MEL-Ma-Mel-05 COSM1167841 c.5150_5151insT p.L1718fs*16 Insertion - Frameshift 14:88621164-88621165 - TCGA-EE-A2A5-06 COSM3498571 c.2330C>T p.A777V Substitution - Missense 14:88696861-88696861 - SC_9047 COSM5556745 c.2388T>C p.H796H Substitution - coding silent 14:88695411-88695411 - LUAD-5V8LT COSM401506 c.574G>T p.G192C Substitution - Missense 14:88740524-88740524 - CSCC-49-T COSM4573208 c.2185_2186GA>TT p.D729F Substitution - Missense 14:88702498-88702499 - CHC1629T COSM4791904 c.4004G>T p.R1335M Substitution - Missense 14:88657376-88657376 - TCGA-E2-A152-01 COSM433450 c.4864G>A p.D1622N Substitution - Missense 14:88625004-88625004 - S02139 COSM5674170 c.22A>T p.S8C Substitution - Missense 14:88792482-88792482 - ESO-159 COSM1251170 c.2980C>T p.Q994* Substitution - Nonsense 14:88685017-88685017 - TCGA-FW-A3TV-06 COSM3498573 c.2144G>A p.R715Q Substitution - Missense 14:88702540-88702540 - TCGA-EE-A2GP-06 COSM3498593 c.306G>A p.K102K Substitution - coding silent 14:88754563-88754563 - HCA7 COSM2250567 c.3477_3478insA p.Q1160fs*25 Insertion - Frameshift 14:88663051-88663052 - I2L-P19Tb-Tumor-Organoid COSM5362327 c.4238-5delT p.? Unknown 14:88638912-88638912 - CHC1629T COSM4791904 c.4004G>T p.R1335M Substitution - Missense 14:88657376-88657376 - TCGA-AA-A010-01 COSM280788 c.2811G>T p.K937N Substitution - Missense 14:88687259-88687259 - CSCC-18-T COSM4552516 c.5618G>A p.R1873K Substitution - Missense 14:88618252-88618252 - TCGA-BR-8368-01 COSM4052841 c.1197G>A p.T399T Substitution - coding silent 14:88715186-88715186 - LUAD-S01302 COSM395561 c.399T>A p.C133* Substitution - Nonsense 14:88746242-88746242 - TCGA-60-2713-01 COSM699158 c.3976C>T p.Q1326* Substitution - Nonsense 14:88657404-88657404 - ICGC_0043 COSM218468 c.4062G>T p.E1354D Substitution - Missense 14:88644478-88644478 - DLD1 COSM2250539 c.4618G>C p.V1540L Substitution - Missense 14:88626960-88626960 - CHC892T COSM4798307 c.3076G>A p.D1026N Substitution - Missense 14:88681938-88681938 - TCGA-B5-A0JY-01 COSM958522 c.3809T>G p.M1270R Substitution - Missense 14:88658255-88658255 - PT13 COSM5896223 c.1636C>T p.R546* Substitution - Nonsense 14:88712292-88712292 - TCGA-BS-A0UF-01 COSM958518 c.4084G>A p.G1362S Substitution - Missense 14:88644456-88644456 - TCGA-21-1071-01 COSM699157 c.2623G>A p.E875K Substitution - Missense 14:88688390-88688390 - LS411 COSM4248037 c.2403G>T p.W801C Substitution - Missense 14:88695396-88695396 - TCGA-EI-7002-01 COSM1735558 c.3206C>T p.A1069V Substitution - Missense 14:88665408-88665408 - SNU-C2B COSM2250600 c.2274A>G p.T758T Substitution - coding silent 14:88696917-88696917 - CN-AML-NR-08-Dx COSM3999397 c.805A>G p.I269V Substitution - Missense 14:88738921-88738921 - CSCC-45-T COSM4459735 c.1138C>T p.H380Y Substitution - Missense 14:88726590-88726590 - ATL050 COSM5705779 c.2438+2T>C p.? Unknown 14:88695359-88695359 - 587376 COSM1205272 c.1215A>C p.K405N Substitution - Missense 14:88715168-88715168 - TCGA-76-6285-01 COSM3401501 c.3399G>A p.W1133* Substitution - Nonsense 14:88664503-88664503 - TCGA-D8-A4Z1-01 COSM3815465 c.4297C>T p.H1433Y Substitution - Missense 14:88638848-88638848 - TCGA-AX-A0J1-01 COSM958540 c.2530C>T p.R844C Substitution - Missense 14:88694316-88694316 - GC_297_T-GC_297_N COSM4772714 c.2743-7delT p.? Unknown 14:88687334-88687334 - TCGA-EE-A3AG-06 COSM3498581 c.1372G>A p.D458N Substitution - Missense 14:88715011-88715011 - TCGA-EI-6917-01 COSM3420080 c.2639C>T p.S880F Substitution - Missense 14:88688374-88688374 - CHEWS008 COSM4578048 c.1044G>T p.S348S Substitution - coding silent 14:88736369-88736369 - WA31 COSM239699 c.1115C>T p.A372V Substitution - Missense 14:88726613-88726613 - HCC2998 COSM2250596 c.2340C>A p.F780L Substitution - Missense 14:88696851-88696851 - HCC64 COSM1608036 c.4993C>T p.R1665C Substitution - Missense 14:88622624-88622624 - TCGA-B5-A0JR-01 COSM958538 c.2607A>T p.A869A Substitution - coding silent 14:88688406-88688406 - TCGA-CA-6717-01 COSM1371443 c.5514C>A p.F1838L Substitution - Missense 14:88618674-88618674 - ATL059 COSM5705781 c.1792A>C p.K598Q Substitution - Missense 14:88706292-88706292 - TCGA-18-4721-01 COSM699154 c.2224G>C p.V742L Substitution - Missense 14:88702460-88702460 - 8044594 COSM3386721 c.2598G>T p.M866I Substitution - Missense 14:88688415-88688415 - DLD1 COSM4623034 c.2572G>T p.G858C Substitution - Missense 14:88688441-88688441 - TCGA-13-1509-01 COSM86634 c.804A>G p.P268P Substitution - coding silent 14:88738922-88738922 - TCGA-EB-A430-01 COSM3498567 c.2672G>A p.R891K Substitution - Missense 14:88688341-88688341 - T1764 COSM4680906 c.5462_5464delACA p.N1821delN Deletion - In frame 14:88618724-88618726 - HCC84T COSM1608039 c.7_8insG p.A3fs*70 Insertion - Frameshift 14:88792496-88792497 - TCGA-D1-A103-01 COSM958497 c.5879C>T p.A1960V Substitution - Missense 14:88616160-88616160 - SC_9047 COSM5567470 c.4768A>G p.S1590G Substitution - Missense 14:88625100-88625100 - RK159_C01 COSM1629421 c.3676-3T>C p.? Unknown 14:88658391-88658391 - BK0026 COSM4186560 c.2906G>T p.G969V Substitution - Missense 14:88685091-88685091 - PT48 COSM5933278 c.3838G>A p.D1280N Substitution - Missense 14:88658226-88658226 - sysucc-311T COSM5478780 c.3410-10T>G p.? Unknown 14:88663129-88663129 - J30_T COSM3956266 c.2531G>T p.R844L Substitution - Missense 14:88694315-88694315 - KYSE-180 COSM4439526 c.2565C>G p.G855G Substitution - coding silent 14:88688448-88688448 - ACINAR03 COSM1735558 c.3206C>T p.A1069V Substitution - Missense 14:88665408-88665408 - PDA_033 COSM4999708 c.678C>G p.I226M Substitution - Missense 14:88740420-88740420 - TCGA-B0-5701-01 COSM3361257 c.2109G>C p.V703V Substitution - coding silent 14:88702575-88702575 - BHY COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - T3724 COSM4680908 c.4844C>A p.A1615D Substitution - Missense 14:88625024-88625024 - PDA_004 COSM4997899 c.3103G>T p.A1035S Substitution - Missense 14:88681911-88681911 - AOCS-142-3-5 COSM3943912 c.852G>T p.L284F Substitution - Missense 14:88736561-88736561 - PD4100a COSM160698 c.461T>G p.F154C Substitution - Missense 14:88744087-88744087 - BD120T COSM5514678 c.3521C>T p.S1174L Substitution - Missense 14:88661808-88661808 - TCGA-AA-A010-01 COSM280786 c.5850T>C p.F1950F Substitution - coding silent 14:88616189-88616189 - TCGA-BS-A0UV-01 COSM244250 c.4723G>A p.A1575T Substitution - Missense 14:88626855-88626855 - CN-AML-08-T COSM3999397 c.805A>G p.I269V Substitution - Missense 14:88738921-88738921 - 1N29-VS-1T29 COSM4052841 c.1197G>A p.T399T Substitution - coding silent 14:88715186-88715186 - TCGA-AP-A0LM-01 COSM958560 c.703G>A p.A235T Substitution - Missense 14:88740395-88740395 - TCGA-BH-A0BZ-01 COSM433451 c.4834C>T p.P1612S Substitution - Missense 14:88625034-88625034 - TCGA-AX-A0J1-01 COSM958528 c.3096T>C p.C1032C Substitution - coding silent 14:88681918-88681918 - E11 COSM1666351 c.4776T>A p.D1592E Substitution - Missense 14:88625092-88625092 - 8069446 COSM3769520 c.2056A>C p.R686R Substitution - coding silent 14:88702628-88702628 - PD8969a COSM5789413 c.5293G>C p.G1765R Substitution - Missense 14:88620836-88620836 - RK101_C01 COSM3700910 c.2454G>A p.K818K Substitution - coding silent 14:88694392-88694392 - 406 COSM4430167 c.2198T>C p.L733P Substitution - Missense 14:88702486-88702486 - sysucc-1370T COSM5470308 c.3733C>T p.R1245C Substitution - Missense 14:88658331-88658331 - UD-SCC-2 COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - TCGA-B7-5816-01 COSM3968952 c.2584A>G p.K862E Substitution - Missense 14:88688429-88688429 - 41T COSM1629423 c.2440G>A p.G814R Substitution - Missense 14:88694406-88694406 - TCGA-AR-A5QQ-01 COSM3815469 c.2335G>A p.D779N Substitution - Missense 14:88696856-88696856 - TCGA-BF-A3DN-01 COSM3498551 c.4678G>A p.G1560R Substitution - Missense 14:88626900-88626900 - CN-AML-08-T COSM5426025 c.5094C>T p.N1698N Substitution - coding silent 14:88621221-88621221 - TCGA-B5-A0JY-01 COSM958524 c.3678G>T p.G1226G Substitution - coding silent 14:88658386-88658386 - TCGA-AA-A010-01 COSM280789 c.689G>A p.R230Q Substitution - Missense 14:88740409-88740409 - OSCC-GB_00410111 COSM1629423 c.2440G>A p.G814R Substitution - Missense 14:88694406-88694406 - HCT15 COSM2250539 c.4618G>C p.V1540L Substitution - Missense 14:88626960-88626960 - 52 COSM5734741 c.579G>C p.K193N Substitution - Missense 14:88740519-88740519 - WSU-HN6 COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - TCGA-BH-A0EE-01 COSM433454 c.1558G>A p.D520N Substitution - Missense 14:88712370-88712370 - ESO-682 COSM1251171 c.5717C>T p.S1906F Substitution - Missense 14:88616805-88616805 - PT48 COSM5933282 c.2209C>T p.P737S Substitution - Missense 14:88702475-88702475 - TCGA-AM-5821-01 COSM3754144 c.2949G>T p.V983V Substitution - coding silent 14:88685048-88685048 - TCGA-60-2726-01 COSM699153 c.1356T>C p.S452S Substitution - coding silent 14:88715027-88715027 - TCGA-EE-A2GO-06 COSM3498591 c.563G>A p.R188Q Substitution - Missense 14:88740535-88740535 - WSU-HN12 COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - T636 COSM2250560 c.3969T>C p.P1323P Substitution - coding silent 14:88657411-88657411 - TCGA-FG-8191-01 COSM3968950 c.4671C>G p.S1557R Substitution - Missense 14:88626907-88626907 - CRC-39T COSM5453215 c.778C>T p.R260C Substitution - Missense 14:88738948-88738948 - PT08_1 COSM5893765 c.4899G>A p.P1633P Substitution - coding silent 14:88622718-88622718 - TCGA-EE-A2MU-06 COSM3498551 c.4678G>A p.G1560R Substitution - Missense 14:88626900-88626900 - TCGA-EE-A29E-06 COSM3498577 c.1528G>A p.G510R Substitution - Missense 14:88712400-88712400 - TCGA-E2-A14Q-01 COSM433452 c.4436delG p.G1479fs*19 Deletion - Frameshift 14:88627741-88627741 - 8015553 COSM218468 c.4062G>T p.E1354D Substitution - Missense 14:88644478-88644478 - AOCS-075-1-0 COSM3943908 c.3823G>C p.E1275Q Substitution - Missense 14:88658241-88658241 - TCGA-A8-A09Z-01 COSM3815471 c.857T>C p.V286A Substitution - Missense 14:88736556-88736556 - 2492712 COSM260681 c.5053G>A p.E1685K Substitution - Missense 14:88621262-88621262 - YUPAER COSM5382794 c.2080C>T p.L694L Substitution - coding silent 14:88702604-88702604 - TCGA-AA-A010-01 COSM299195 c.5898-7A>G p.? Unknown 14:88615861-88615861 - TCGA-AO-A03M-01 COSM3815473 c.457-1G>A p.? Unknown 14:88744092-88744092 - HCC64T COSM1608036 c.4993C>T p.R1665C Substitution - Missense 14:88622624-88622624 - TCGA-BR-A4CQ-01 COSM4052832 c.3402T>C p.D1134D Substitution - coding silent 14:88664500-88664500 - TCGA-D1-A17Q-01 COSM958550 c.1797G>T p.L599L Substitution - coding silent 14:88706287-88706287 - TCGA-BR-8297-01 COSM4052837 c.2223C>G p.Y741* Substitution - Nonsense 14:88702461-88702461 - 61 COSM5740191 c.3410-1G>T p.? Unknown 14:88663120-88663120 - C086 COSM5530452 c.832G>A p.D278N Substitution - Missense 14:88738894-88738894 - PT08_1 COSM5893764 c.4022G>T p.G1341V Substitution - Missense 14:88646953-88646953 - L3230 COSM1745021 c.1561A>G p.I521V Substitution - Missense 14:88712367-88712367 - PCSI_0357_Pa_P_5263 COSM4806584 c.4612G>T p.V1538F Substitution - Missense 14:88626966-88626966 - TCGA-43-5668-01 COSM699159 c.4268A>G p.D1423G Substitution - Missense 14:88638877-88638877 - 421 COSM2250508 c.5933G>A p.*1978* Substitution - coding silent 14:88615819-88615819 - CHC896T COSM4953578 c.233C>A p.T78K Substitution - Missense 14:88754636-88754636 - CSCC-60-T COSM4568623 c.1249T>G p.S417A Substitution - Missense 14:88715134-88715134 - HCA7 COSM4630090 c.5392C>T p.R1798W Substitution - Missense 14:88618796-88618796 - UM-SCC-2 COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - TCGA-EE-A2MR-06 COSM3498547 c.5643-1G>A p.? Unknown 14:88616880-88616880 - SNUH_G45_S1 COSM3999397 c.805A>G p.I269V Substitution - Missense 14:88738921-88738921 - PD11367a COSM5772995 c.2217A>G p.K739K Substitution - coding silent 14:88702467-88702467 - TCGA-G2-A2EO-01 COSM1300878 c.3865G>A p.E1289K Substitution - Missense 14:88658199-88658199 - TCGA-FS-A1ZD-06 COSM3498563 c.3257C>T p.S1086L Substitution - Missense 14:88665357-88665357 - AOCS-083-1-7 COSM3943910 c.1491G>C p.W497C Substitution - Missense 14:88712437-88712437 - STC243 COSM5054132 c.890T>C p.L297P Substitution - Missense 14:88736523-88736523 - BN41 COSM1608037 c.4586T>G p.F1529C Substitution - Missense 14:88626992-88626992 - CSCC-29-T COSM3498551 c.4678G>A p.G1560R Substitution - Missense 14:88626900-88626900 - PD7192a COSM3769804 c.1445G>A p.G482E Substitution - Missense 14:88712483-88712483 - TCGA-AA-3697-01 COSM1371449 c.1109G>A p.R370H Substitution - Missense 14:88726619-88726619 - TCGA-AX-A05Z-01 COSM958554 c.1406A>C p.N469T Substitution - Missense 14:88714977-88714977 - RK130_C01 COSM1629422 c.2613T>C p.Y871Y Substitution - coding silent 14:88688400-88688400 - 587226 COSM1205265 c.4361C>T p.T1454I Substitution - Missense 14:88627816-88627816 - PR-09-5700 COSM244250 c.4723G>A p.A1575T Substitution - Missense 14:88626855-88626855 - TCGA-D1-A17B-01 COSM958507 c.5651_5653delGAG p.G1884delG Deletion - In frame 14:88616869-88616871 - S02285 COSM5684551 c.2434G>T p.A812S Substitution - Missense 14:88695365-88695365 - 587230 COSM1205273 c.1090A>C p.N364H Substitution - Missense 14:88726638-88726638 - YUNIBO COSM5382792 c.2737G>A p.E913K Substitution - Missense 14:88688276-88688276 - CSCC-32-T COSM4540461 c.2846G>A p.G949E Substitution - Missense 14:88687224-88687224 - 587376 COSM1205271 c.5288A>C p.K1763T Substitution - Missense 14:88620841-88620841 - LUAD-NYU284 COSM372771 c.3709C>T p.H1237Y Substitution - Missense 14:88658355-88658355 - PT48 COSM5933280 c.2860C>T p.L954F Substitution - Missense 14:88685137-88685137 - OSCC-GB_00860111 COSM4885340 c.2489A>T p.D830V Substitution - Missense 14:88694357-88694357 - TCGA-AQ-A54O-01 COSM3815467 c.2663G>A p.C888Y Substitution - Missense 14:88688350-88688350 - pfg068T COSM4758603 c.4693C>A p.L1565M Substitution - Missense 14:88626885-88626885 - 37M COSM5583477 c.4208C>T p.S1403F Substitution - Missense 14:88642922-88642922 - LUAD-B00416 COSM330937 c.2992G>T p.E998* Substitution - Nonsense 14:88682022-88682022 - TCGA-AX-A05Z-01 COSM958546 c.2032C>T p.R678* Substitution - Nonsense 14:88704879-88704879 - TCGA-BR-6452-01 COSM4052839 c.1950A>G p.L650L Substitution - coding silent 14:88704961-88704961 - TCGA-BH-A1EN-01 COSM1477817 c.729G>A p.M243I Substitution - Missense 14:88738997-88738997 - PD24325a COSM5781230 c.217C>G p.R73G Substitution - Missense 14:88754652-88754652 - HN_62601 COSM122834 c.256T>C p.Y86H Substitution - Missense 14:88754613-88754613 - TCGA-C8-A26Y-01 COSM3815463 c.5521G>C p.D1841H Substitution - Missense 14:88618667-88618667 - GC_315T-GC_315N COSM4773855 c.420A>G p.G140G Substitution - coding silent 14:88746221-88746221 - TCGA-EE-A181-06 COSM3498565 c.2845G>A p.G949R Substitution - Missense 14:88687225-88687225 - 587234 COSM1205270 c.5422T>C p.S1808P Substitution - Missense 14:88618766-88618766 - 180 COSM3721626 c.1255G>C p.D419H Substitution - Missense 14:88715128-88715128 - 172T COSM1725912 c.818A>C p.D273A Substitution - Missense 14:88738908-88738908 - TCGA-FU-A3HY-01 COSM4838637 c.1366C>T p.H456Y Substitution - Missense 14:88715017-88715017 - CHC896T COSM4953578 c.233C>A p.T78K Substitution - Missense 14:88754636-88754636 - TCGA-RP-A695-06 COSM4896921 c.4579G>A p.A1527T Substitution - Missense 14:88626999-88626999 - CSCC-32-T COSM4539348 c.2674G>A p.D892N Substitution - Missense 14:88688339-88688339 - TCGA-18-5592-01 COSM699151 c.1175T>C p.V392A Substitution - Missense 14:88726553-88726553 - TCGA-BS-A0TA-01 COSM958499 c.5872_5874delGTT p.V1958delV Deletion - In frame 14:88616165-88616167 - MO_1014 COSM5552724 c.3442G>C p.E1148Q Substitution - Missense 14:88663087-88663087 - TCGA-AP-A059-01 COSM958542 c.2398C>T p.L800F Substitution - Missense 14:88695401-88695401 - RMS106_ COSM4986515 c.3562C>A p.P1188T Substitution - Missense 14:88661767-88661767 - TCGA-AX-A0J0-01 COSM958509 c.5618G>T p.R1873I Substitution - Missense 14:88618252-88618252 - 93VU147T COSM4591672 c.128T>G p.V43G Substitution - Missense 14:88792376-88792376 - ESOSCC158T COSM1172236 c.2752A>G p.T918A Substitution - Missense 14:88687318-88687318 - TCGA-EE-A2GO-06 COSM3498579 c.1526A>T p.N509I Substitution - Missense 14:88712402-88712402 - 824_T COSM3956268 c.2484G>C p.V828V Substitution - coding silent 14:88694362-88694362 - TCGA-CG-5721-01 COSM4052824 c.4849T>C p.Y1617H Substitution - Missense 14:88625019-88625019 - TCGA-DK-A1AB-01 COSM416581 c.2214G>C p.L738F Substitution - Missense 14:88702470-88702470 - CHC892T COSM4797326 c.1050G>A p.R350R Substitution - coding silent 14:88726678-88726678 - C0019T COSM4150863 c.572T>C p.F191S Substitution - Missense 14:88740526-88740526 - TCGA-BR-4362-01 COSM4052822 c.4867G>A p.G1623R Substitution - Missense 14:88625001-88625001 - LUAD-CHTN-MAD06-00668 COSM358880 c.3361T>C p.C1121R Substitution - Missense 14:88664541-88664541 - Pat_76_A COSM5848651 c.5878G>T p.A1960S Substitution - Missense 14:88616161-88616161 - T84 COSM2250592 c.2512A>C p.K838Q Substitution - Missense 14:88694334-88694334 - TCGA-DK-A3WW-01 COSM3793919 c.3272C>T p.S1091L Substitution - Missense 14:88665342-88665342 - 8051900 COSM3386719 c.5013A>C p.K1671N Substitution - Missense 14:88622604-88622604 - KPOPBR-03-T COSM5965400 c.2072G>A p.R691Q Substitution - Missense 14:88702612-88702612 - TCGA-BP-5190-01 COSM470320 c.2246G>T p.R749I Substitution - Missense 14:88696945-88696945 - S02292 COSM5687445 c.3748G>T p.D1250Y Substitution - Missense 14:88658316-88658316 - 6115114 COSM5570694 c.401T>C p.V134A Substitution - Missense 14:88746240-88746240 - TCGA-D3-A3C7-06 COSM3498589 c.592C>T p.Q198* Substitution - Nonsense 14:88740506-88740506 - HCC153 COSM3706424 c.1932+3A>G p.? Unknown 14:88705479-88705479 - T3262 COSM4680912 c.3499G>A p.V1167I Substitution - Missense 14:88661830-88661830 - LUAD_E00522 COSM388706 c.501C>T p.V167V Substitution - coding silent 14:88744047-88744047 - TCGA-AA-3966-01 COSM272638 c.3313A>G p.S1105G Substitution - Missense 14:88664589-88664589 - S01366 COSM5668016 c.2081T>C p.L694P Substitution - Missense 14:88702603-88702603 - TCGA-EE-A2MS-06 COSM3498575 c.1790G>A p.R597K Substitution - Missense 14:88706294-88706294 - TCGA-EJ-5503-01 COSM1128179 c.5783G>A p.C1928Y Substitution - Missense 14:88616739-88616739 - TCGA-ER-A198-06 COSM3498549 c.4888A>T p.K1630* Substitution - Nonsense 14:88624980-88624980 - TCGA-DC-6154-01 COSM3420083 c.435G>T p.M145I Substitution - Missense 14:88746206-88746206 - TCGA-B0-4713-01 COSM3361259 c.889C>G p.L297V Substitution - Missense 14:88736524-88736524 - RK277_C01 COSM4946483 c.5749G>T p.D1917Y Substitution - Missense 14:88616773-88616773 - TCGA-24-1604-01 COSM86633 c.2869G>T p.D957Y Substitution - Missense 14:88685128-88685128 - HCC153T COSM3706424 c.1932+3A>G p.? Unknown 14:88705479-88705479 - OSCC-GB_01080111 COSM4884425 c.4430C>G p.S1477* Substitution - Nonsense 14:88627747-88627747 - S02292 COSM5687447 c.358C>A p.R120S Substitution - Missense 14:88746283-88746283 - TCGA-AP-A051-01 COSM958556 c.1319G>A p.R440H Substitution - Missense 14:88715064-88715064 - SW48 COSM2250590 c.2553T>C p.I851I Substitution - coding silent 14:88688460-88688460 - HCT116 COSM2250543 c.4575delT p.F1525fs*18 Deletion - Frameshift 14:88627003-88627003 - TCGA-ER-A19P-06 COSM3498553 c.4606C>G p.Q1536E Substitution - Missense 14:88626972-88626972 - CSCC-49-T COSM4538238 c.2520G>A p.M840I Substitution - Missense 14:88694326-88694326 - TCGA-A2-A04N-01 COSM433453 c.1673A>T p.K558I Substitution - Missense 14:88706411-88706411 - TCGA-BR-8361-01 COSM280789 c.689G>A p.R230Q Substitution - Missense 14:88740409-88740409 - ESCC-153T COSM3936647 c.1882G>C p.E628Q Substitution - Missense 14:88705532-88705532 - TCGA-FJ-A3ZE-01 COSM3793921 c.3030G>A p.L1010L Substitution - coding silent 14:88681984-88681984 - 10-276 COSM3736747 c.1258G>A p.G420R Substitution - Missense 14:88715125-88715125 - 587342 COSM1205269 c.3239A>G p.H1080R Substitution - Missense 14:88665375-88665375 - TCGA-Q1-A6DV-01 COSM4850929 c.3306C>A p.S1102S Substitution - coding silent 14:88664596-88664596 - TCGA-DD-A3A9-01 COSM4920655 c.980A>T p.E327V Substitution - Missense 14:88736433-88736433 - TCGA-BW-A5NQ-01 COSM3498591 c.563G>A p.R188Q Substitution - Missense 14:88740535-88740535 - TCGA-FS-A1ZK-06 COSM3498561 c.3266G>A p.R1089Q Substitution - Missense 14:88665348-88665348 - 40M COSM5585097 c.3214C>T p.L1072L Substitution - coding silent 14:88665400-88665400 - TCGA-AG-A002-01 COSM260680 c.5845C>T p.R1949* Substitution - Nonsense 14:88616194-88616194 - TCGA-D3-A1Q6-06 COSM3498570 c.2628G>A p.E876E Substitution - coding silent 14:88688385-88688385 - TCGA-HU-A4H3-01 COSM4052834 c.2819C>T p.A940V Substitution - Missense 14:88687251-88687251 - CSB1 COSM5027899 c.669G>C p.W223C Substitution - Missense 14:88740429-88740429 - TCGA-HT-8558-01 COSM3968952 c.2584A>G p.K862E Substitution - Missense 14:88688429-88688429 - T2269 COSM4680918 c.2459T>G p.F820C Substitution - Missense 14:88694387-88694387 - TCGA-EE-A3JA-06 COSM1205266 c.875G>A p.R292Q Substitution - Missense 14:88736538-88736538 - T578 COSM4680922 c.518A>C p.H173P Substitution - Missense 14:88744030-88744030 - YUROG COSM5382802 c.555C>T p.T185T Substitution - coding silent 14:88740543-88740543 - TCGA-EE-A2MT-06 COSM3498557 c.4165C>T p.H1389Y Substitution - Missense 14:88642965-88642965 - TCGA-DI-A0WH-01 COSM958516 c.4238-2A>G p.? Unknown 14:88638909-88638909 - TCGA-H4-A2HQ-01 COSM1300877 c.4145G>C p.R1382T Substitution - Missense 14:88642985-88642985 - STC246 COSM5054130 c.1497A>G p.S499S Substitution - coding silent 14:88712431-88712431 - CHOL12 COSM1743251 c.3877G>A p.G1293S Substitution - Missense 14:88658187-88658187 - AOCS-145-1-6 COSM3943904 c.5511C>G p.D1837E Substitution - Missense 14:88618677-88618677 - TCGA-BP-4770-01 COSM470319 c.2393T>C p.V798A Substitution - Missense 14:88695406-88695406 - PD6719a COSM5792845 c.1313C>T p.A438V Substitution - Missense 14:88715070-88715070 - AOCS-095-3-1 COSM3943906 c.3933A>G p.L1311L Substitution - coding silent 14:88657447-88657447 - S02255 COSM5680502 c.2255C>T p.S752L Substitution - Missense 14:88696936-88696936 - 1N03-VS-1T03 COSM4972590 c.3202A>T p.N1068Y Substitution - Missense 14:88665412-88665412 - TCGA-AU-6004-01 COSM1371442 c.5825C>T p.S1942L Substitution - Missense 14:88616214-88616214 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.325846 14q31.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAC - InFrameDeletion p.V1958delV c.5872_5874delGTT 14 89082509 UCEC A C Missense p.F154C c.461T>G 14 89210431 BRCA A C Missense p.F879V c.2635T>G 14 89154722 CM A C Synonymous p.S1094S c.3282T>G 14 89130964 CM - A Frameshift p.L1718Pfs*16 c.5150dupT 14 89087509 CM A G Missense p.C1750R c.5248T>C 14 89087225 LUSC A G Missense p.I229T c.686T>C 14 89206756 HNSC A G Missense p.L738S c.2213T>C 14 89168815 PRAD A G Missense p.M1920T c.5759T>C 14 89083107 UCEC A G Missense p.V1410A c.4229T>C 14 89109245 ESCA A G Missense p.V1905A c.5714T>C 14 89083152 UCEC A G Missense p.V392A c.1175T>C 14 89192897 LUSC A G Missense p.Y86H c.256T>C 14 89220957 HNSC A G Synonymous p.D1662D c.4986T>C 14 89088975 HNSC A G Synonymous p.S452S c.1356T>C 14 89181371 LUSC A G Synonymous p.Y871Y c.2613T>C 14 89154744 HC A T 3-UTRSNV . c.5931+535T>A 14 89081630 MB A T Missense p.Y704N c.2110T>A 14 89168918 RCCC C A Missense p.D728Y c.2182G>T 14 89168846 HNSC C A Missense p.D957Y c.2869G>T 14 89151472 OV C A Missense p.E1354D c.4062G>T 14 89110822 PAAD C A Missense p.G847V c.2540G>T 14 89154817 LUAD C A Missense p.V1178L c.3532G>T 14 89128141 RCCC C A Missense p.V333F c.997G>T 14 89202760 LUSC C A Missense p.V778F c.2332G>T 14 89163203 LUSC - C Frameshift p.E1688Rfs*7 c.5060dupG 14 89087599 LUAD C - Frameshift p.G1479Efs*19 c.4436delG 14 89094085 BRCA C - Frameshift p.G449Dfs*38 c.1346delG 14 89181381 LUAD C G Missense p.L738F c.2214G>C 14 89168814 BLCA C G Missense p.R1382T c.4145G>C 14 89109329 BLCA C G Missense p.R350T c.1049G>C 14 89202708 RCCC C G Missense p.V742L c.2224G>C 14 89168804 LUSC C G Missense p.W223C c.669G>C 14 89206773 BRCA C G Synonymous p.V703V c.2109G>C 14 89168919 RCCC CTC - InFrameDeletion p.G1884delG c.5651_5653delGAG 14 89083213 UCEC C T IntronicSNV . c.1187+4327G>A 14 89188558 PIA C T Missense p.C1928Y c.5783G>A 14 89083083 PRAD C T Missense p.D1051N c.3151G>A 14 89131807 HNSC C T Missense p.D1622N c.4864G>A 14 89091348 BRCA C T Missense p.D458N c.1372G>A 14 89181355 CM C T Missense p.D520N c.1558G>A 14 89178714 BRCA C T Missense p.E1289K c.3865G>A 14 89124543 BLCA C T Missense p.E875K c.2623G>A 14 89154734 LUSC C T Missense p.G1511S c.4531G>A 14 89093990 CM C T Missense p.G1541E c.4622G>A 14 89093300 CM C T Missense p.G1560R c.4678G>A 14 89093244 CM C T Missense p.G1579D c.4736G>A 14 89093186 RCCC C T Missense p.G814R c.2440G>A 14 89160750 HC C T Missense p.G949R c.2845G>A 14 89153569 CM C T Missense p.G995E c.2984G>A 14 89148374 CM C T Missense p.M243I c.729G>A 14 89205341 BRCA C T Missense p.R1089Q c.3266G>A 14 89131692 CM C T Missense p.R1245H c.3734G>A 14 89124674 HNSC C T Missense p.R188Q c.563G>A 14 89206879 CM C T Missense p.R292Q c.875G>A 14 89202882 CM C T Missense p.R597K c.1790G>A 14 89172638 CM C T Missense p.R715Q c.2144G>A 14 89168884 CM C T Missense p.V1957I c.5869G>A 14 89082514 HNSC C T Nonsense p.W1133* c.3399G>A 14 89130847 GBM C T Synonymous p.A1606A c.4818G>A 14 89091394 HNSC C T Synonymous p.A782A c.2346G>A 14 89161797 STAD C T Synonymous p.E1166E c.3498G>A 14 89129375 OV C T Synonymous p.E876E c.2628G>A 14 89154729 CM C T Synonymous p.K102K c.306G>A 14 89220907 CM G A 5-UTRSNV . c.1-176C>T 14 89259023 DLBCL G A IntronicSNV . c.4029-79C>T 14 89110934 CM G A IntronicSNV . c.4358-1594C>T 14 89095757 PIA G A IntronicSNV . c.5376-447C>T 14 89085603 DLBCL G A Missense p.A777V c.2330C>T 14 89163205 CM G A Missense p.H1130Y c.3388C>T 14 89130858 CM G A Missense p.H1389Y c.4165C>T 14 89109309 CM G A Missense p.P1456S c.4366C>T 14 89094155 CM G A Missense p.P1612S c.4834C>T 14 89091378 BRCA G A Missense p.P548S c.1642C>T 14 89178630 CM G A Missense p.P826S c.2476C>T 14 89160714 CM G A Missense p.R1316C c.3946C>T 14 89123778 CM G A Missense p.R347C c.1039C>T 14 89202718 CM G A Missense p.S1086L c.3257C>T 14 89131701 CM G A Missense p.S1906F c.5717C>T 14 89083149 ESCA G A Nonsense p.Q1326* c.3976C>T 14 89123748 LUSC G A Nonsense p.Q198* c.592C>T 14 89206850 CM G A Nonsense p.Q994* c.2980C>T 14 89151361 ESCA G A Nonsense p.R691* c.2071C>T 14 89168957 CM G A Synonymous p.A1869A c.5607C>T 14 89084607 GBM G A Synonymous p.T1021T c.3063C>T 14 89148295 CM G A Synonymous p.Y741Y c.2223C>T 14 89168805 GBM G C Missense p.I1788M c.5364C>G 14 89087109 ESCA G C Missense p.L1256V c.3766C>G 14 89124642 CM G C Missense p.L297V c.889C>G 14 89202868 RCCC G C Missense p.Q1536E c.4606C>G 14 89093316 CM G C Missense p.R370G c.1108C>G 14 89192964 HNSC G C Missense p.S1102C c.3305C>G 14 89130941 HNSC G C Missense p.S1557R c.4671C>G 14 89093251 LGG GG AA Missense p.T185I c.554_555delinsTT 14 89206887 CM G - IntronicDeletion . c.1188-47delC 14 89181586 ESCA G T Missense p.A1527E c.4580C>A 14 89093342 LUAD G T Nonsense p.S123* c.368C>A 14 89212617 BRCA G T Synonymous p.L936L c.2808C>A 14 89153606 BRCA T A Missense p.K1276I c.3827A>T 14 89124581 COREAD T A Missense p.K558I c.1673A>T 14 89172755 BRCA T A Missense p.K831N c.2493A>T 14 89160697 MM T A Missense p.N509I c.1526A>T 14 89178746 CM T A Nonsense p.K1630* c.4888A>T 14 89091324 CM T A Nonsense p.R1873* c.5617A>T 14 89084597 CM T A Synonymous p.A869A c.2607A>T 14 89154750 UCEC T C Missense p.D1423G c.4268A>G 14 89105221 LUSC T C Missense p.K862E c.2584A>G 14 89154773 STAD T C Missense p.K985E c.2953A>G 14 89151388 CM T C Synonymous p.P268P c.804A>G 14 89205266 OV - T Frameshift p.S663Kfs*5 c.1987dupA 14 89171268 HNSC