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 11 66888787 66888787 + De_novo_Start_InFrame SNP G G A TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chr11:66888787G>A BLCA 11 66888808 66888808 + Silent SNP G G A TCGA-XF-A9SV-01A-21D-A42E-08 TCGA-XF-A9SV-10A-01D-A42H-08 g.chr11:66888808G>A c.21G>A c.(19-21)agG>agA p.R7R BLCA 11 66975111 66975111 + Silent SNP C C G TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr11:66975111C>G c.438C>G c.(436-438)ctC>ctG p.L146L BLCA 11 67017821 67017821 + Missense_Mutation SNP C C T TCGA-CF-A1HS-01A-11D-A13W-08 TCGA-CF-A1HS-10A-01D-A13W-08 g.chr11:67017821C>T c.2320C>T c.(2320-2322)Cgg>Tgg p.R774W BLCA 11 67020969 67020969 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr11:67020969C>G c.2978C>G c.(2977-2979)tCt>tGt p.S993C BLCA 11 67021043 67021043 + Missense_Mutation SNP C C G TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr11:67021043C>G c.3052C>G c.(3052-3054)Caa>Gaa p.Q1018E BLCA 11 67021049 67021049 + Missense_Mutation SNP C C T TCGA-BT-A20T-01A-11D-A14W-08 TCGA-BT-A20T-11A-11D-A14W-08 g.chr11:67021049C>T c.3058C>T c.(3058-3060)Cgg>Tgg p.R1020W BLCA 11 67022358 67022358 + Missense_Mutation SNP G G C TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr11:67022358G>C c.3321G>C c.(3319-3321)ttG>ttC p.L1107F BLCA 11 67022406 67022406 + Silent SNP G G A TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr11:67022406G>A c.3369G>A c.(3367-3369)ttG>ttA p.L1123L BRCA 11 66947566 66947566 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:66947566G>A c.59G>A c.(58-60)cGa>cAa p.R20Q BRCA 11 66985342 66985342 + Silent SNP C C T TCGA-E2-A2P6-01A-11D-A19Y-09 TCGA-E2-A2P6-10B-01D-A19Y-09 g.chr11:66985342C>T c.828C>T c.(826-828)ttC>ttT p.F276F BRCA 11 66995613 66995613 + Nonsense_Mutation SNP C C T TCGA-A2-A1G4-01A-11D-A13L-09 TCGA-A2-A1G4-10A-01W-A14R-09 g.chr11:66995613C>T c.1063C>T c.(1063-1065)Cag>Tag p.Q355* BRCA 11 66999259 66999259 + Missense_Mutation SNP G G A TCGA-EW-A1PB-01A-11D-A142-09 TCGA-EW-A1PB-10A-01D-A142-09 g.chr11:66999259G>A c.1307G>A c.(1306-1308)gGa>gAa p.G436E BRCA 11 66999270 66999270 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:66999270G>A c.1318G>A c.(1318-1320)Gat>Aat p.D440N BRCA 11 67010479 67010479 + Splice_Site SNP G G T TCGA-BH-A1ET-01A-11D-A135-09 TCGA-BH-A1ET-11B-23D-A135-09 g.chr11:67010479G>T c.e13-1 BRCA 11 67012672 67012672 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:67012672A>C c.1576A>C c.(1576-1578)Act>Cct p.T526P BRCA 11 67012699 67012699 + Missense_Mutation SNP A A G TCGA-E9-A5UO-01A-11D-A28B-09 TCGA-E9-A5UO-10A-01D-A28E-09 g.chr11:67012699A>G c.1603A>G c.(1603-1605)Atc>Gtc p.I535V BRCA 11 67017996 67017996 + Frame_Shift_Del DEL C C - TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr11:67017996delC c.2495delC c.(2494-2496)tccfs p.S832fs BRCA 11 67018032 67018032 + Frame_Shift_Del DEL C C - TCGA-E9-A1NA-01A-11D-A142-09 TCGA-E9-A1NA-10A-01D-A142-09 g.chr11:67018032delC c.2531delC c.(2530-2532)accfs p.T844fs BRCA 11 67020978 67020978 + Missense_Mutation SNP G G A TCGA-E2-A1B0-01A-11D-A12Q-09 TCGA-E2-A1B0-10A-01D-A12Q-09 g.chr11:67020978G>A c.2987G>A c.(2986-2988)aGc>aAc p.S996N CESC 11 66975046 66975046 + Nonsense_Mutation SNP C C T TCGA-EK-A2PL-01A-11D-A18J-09 TCGA-EK-A2PL-10A-01D-A18J-09 g.chr11:66975046C>T c.373C>T c.(373-375)Cag>Tag p.Q125* CESC 11 66975079 66975079 + Missense_Mutation SNP G G A TCGA-C5-A1MN-01A-11D-A14W-08 TCGA-C5-A1MN-10A-01D-A14W-08 g.chr11:66975079G>A c.406G>A c.(406-408)Gag>Aag p.E136K CESC 11 66975147 66975147 + Silent SNP G G A TCGA-EK-A2RA-01A-11D-A18J-09 TCGA-EK-A2RA-10A-01D-A18J-09 g.chr11:66975147G>A c.474G>A c.(472-474)caG>caA p.Q158Q CESC 11 66995615 66995615 + Missense_Mutation SNP G G C TCGA-EK-A3GM-01A-11D-A20U-09 TCGA-EK-A3GM-10A-01D-A20U-09 g.chr11:66995615G>C c.1065G>C c.(1063-1065)caG>caC p.Q355H CESC 11 66999107 66999107 + Missense_Mutation SNP G G C TCGA-EK-A3GM-01A-11D-A20U-09 TCGA-EK-A3GM-10A-01D-A20U-09 g.chr11:66999107G>C c.1155G>C c.(1153-1155)ttG>ttC p.L385F CESC 11 67017739 67017739 + Missense_Mutation SNP C C G TCGA-EK-A2H0-01A-11D-A17W-09 TCGA-EK-A2H0-10A-01D-A17W-09 g.chr11:67017739C>G c.2238C>G c.(2236-2238)agC>agG p.S746R CESC 11 67021785 67021785 + Missense_Mutation SNP G G A TCGA-EA-A5O9-01A-11D-A28B-09 TCGA-EA-A5O9-10A-01D-A28E-09 g.chr11:67021785G>A c.3203G>A c.(3202-3204)cGa>cAa p.R1068Q CESC 11 67021879 67021879 + Silent SNP C C A TCGA-Q1-A6DW-01A-11D-A32I-09 TCGA-Q1-A6DW-10B-01D-A32I-09 g.chr11:67021879C>A c.3297C>A c.(3295-3297)ctC>ctA p.L1099L CESC 11 67022514 67022514 + Silent SNP G G A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr11:67022514G>A c.3477G>A c.(3475-3477)caG>caA p.Q1159Q COAD 11 66975083 66975083 + Missense_Mutation SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:66975083G>A c.410G>A c.(409-411)cGa>cAa p.R137Q COAD 11 66975116 66975116 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:66975116T>G c.443T>G c.(442-444)tTt>tGt p.F148C COAD 11 66983401 66983401 + Missense_Mutation SNP A A G TCGA-CM-5341-01A-01D-1408-10 TCGA-CM-5341-10A-01D-1408-10 g.chr11:66983401A>G c.668A>G c.(667-669)cAc>cGc p.H223R COAD 11 66986811 66986811 + Frame_Shift_Del DEL T T - TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr11:66986811delT c.894delT c.(892-894)aatfs p.N298fs COAD 11 66995525 66995525 + Silent SNP C C T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr11:66995525C>T c.975C>T c.(973-975)cgC>cgT p.R325R COAD 11 67012860 67012860 + Silent SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:67012860C>T c.1764C>T c.(1762-1764)tgC>tgT p.C588C COAD 11 67012916 67012916 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:67012916G>A c.1820G>A c.(1819-1821)cGa>cAa p.R607Q COAD 11 67013527 67013527 + Silent SNP T T C TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:67013527T>C c.1905T>C c.(1903-1905)ttT>ttC p.F635F COAD 11 67017693 67017693 + Frame_Shift_Del DEL C C - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:67017693delC c.2192delC c.(2191-2193)tccfs p.S731fs COAD 11 67017699 67017699 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr11:67017699G>A c.2198G>A c.(2197-2199)cGg>cAg p.R733Q COAD 11 67017880 67017880 + Missense_Mutation SNP G G T TCGA-AA-3812-01A-01W-0900-09 TCGA-AA-3812-10A-01W-0900-09 g.chr11:67017880G>T c.2379G>T c.(2377-2379)aaG>aaT p.K793N COAD 11 67017923 67017923 + Missense_Mutation SNP A A G TCGA-AA-3831-01A-01W-0900-09 TCGA-AA-3831-10A-01W-0900-09 g.chr11:67017923A>G c.2422A>G c.(2422-2424)Aaa>Gaa p.K808E COAD 11 67017996 67017996 + Frame_Shift_Del DEL C C - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr11:67017996delC c.2495delC c.(2494-2496)tccfs p.S832fs COAD 11 67018060 67018060 + Frame_Shift_Del DEL G G - TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr11:67018060delG c.2559delG c.(2557-2559)ctgfs p.L853fs COAD 11 67020274 67020274 + Missense_Mutation SNP A A G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr11:67020274A>G c.2878A>G c.(2878-2880)Agt>Ggt p.S960G COAD 11 67020276 67020276 + Silent SNP T T C TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr11:67020276T>C c.2880T>C c.(2878-2880)agT>agC p.S960S COAD 11 67021715 67021715 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:67021715C>T c.3133C>T c.(3133-3135)Cgg>Tgg p.R1045W COAD 11 67021751 67021751 + Missense_Mutation SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr11:67021751C>T c.3169C>T c.(3169-3171)Cgc>Tgc p.R1057C COAD 11 67021752 67021752 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr11:67021752G>A c.3170G>A c.(3169-3171)cGc>cAc p.R1057H COAD 11 67022388 67022388 + Silent SNP C C T TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr11:67022388C>T c.3351C>T c.(3349-3351)cgC>cgT p.R1117R COADREAD 11 66975083 66975083 + Missense_Mutation SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:66975083G>A c.410G>A c.(409-411)cGa>cAa p.R137Q COADREAD 11 66975116 66975116 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:66975116T>G c.443T>G c.(442-444)tTt>tGt p.F148C COADREAD 11 66983401 66983401 + Missense_Mutation SNP A A G TCGA-CM-5341-01A-01D-1408-10 TCGA-CM-5341-10A-01D-1408-10 g.chr11:66983401A>G c.668A>G c.(667-669)cAc>cGc p.H223R COADREAD 11 66986811 66986811 + Frame_Shift_Del DEL T T - TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr11:66986811delT c.894delT c.(892-894)aatfs p.N298fs COADREAD 11 66995525 66995525 + Silent SNP C C T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr11:66995525C>T c.975C>T c.(973-975)cgC>cgT p.R325R COADREAD 11 67012860 67012860 + Silent SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:67012860C>T c.1764C>T c.(1762-1764)tgC>tgT p.C588C COADREAD 11 67012916 67012916 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:67012916G>A c.1820G>A c.(1819-1821)cGa>cAa p.R607Q COADREAD 11 67013527 67013527 + Silent SNP T T C TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:67013527T>C c.1905T>C c.(1903-1905)ttT>ttC p.F635F COADREAD 11 67017693 67017693 + Frame_Shift_Del DEL C C - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:67017693delC c.2192delC c.(2191-2193)tccfs p.S731fs COADREAD 11 67017699 67017699 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr11:67017699G>A c.2198G>A c.(2197-2199)cGg>cAg p.R733Q COADREAD 11 67017880 67017880 + Missense_Mutation SNP G G T TCGA-AA-3812-01A-01W-0900-09 TCGA-AA-3812-10A-01W-0900-09 g.chr11:67017880G>T c.2379G>T c.(2377-2379)aaG>aaT p.K793N COADREAD 11 67017923 67017923 + Missense_Mutation SNP A A G TCGA-AA-3831-01A-01W-0900-09 TCGA-AA-3831-10A-01W-0900-09 g.chr11:67017923A>G c.2422A>G c.(2422-2424)Aaa>Gaa p.K808E COADREAD 11 67017996 67017996 + Frame_Shift_Del DEL C C - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr11:67017996delC c.2495delC c.(2494-2496)tccfs p.S832fs COADREAD 11 67018060 67018060 + Frame_Shift_Del DEL G G - TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr11:67018060delG c.2559delG c.(2557-2559)ctgfs p.L853fs COADREAD 11 67020274 67020274 + Missense_Mutation SNP A A G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr11:67020274A>G c.2878A>G c.(2878-2880)Agt>Ggt p.S960G COADREAD 11 67020276 67020276 + Silent SNP T T C TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr11:67020276T>C c.2880T>C c.(2878-2880)agT>agC p.S960S COADREAD 11 67021715 67021715 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:67021715C>T c.3133C>T c.(3133-3135)Cgg>Tgg p.R1045W COADREAD 11 67021751 67021751 + Missense_Mutation SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr11:67021751C>T c.3169C>T c.(3169-3171)Cgc>Tgc p.R1057C COADREAD 11 67021752 67021752 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr11:67021752G>A c.3170G>A c.(3169-3171)cGc>cAc p.R1057H COADREAD 11 67022388 67022388 + Silent SNP C C T TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr11:67022388C>T c.3351C>T c.(3349-3351)cgC>cgT p.R1117R ESCA 11 66999063 66999063 + Missense_Mutation SNP G G T TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr11:66999063G>T c.1111G>T c.(1111-1113)Ggg>Tgg p.G371W ESCA 11 66999244 66999244 + Missense_Mutation SNP G G A TCGA-R6-A6DN-01B-11D-A31U-09 TCGA-R6-A6DN-10A-01D-A31U-09 g.chr11:66999244G>A c.1292G>A c.(1291-1293)cGg>cAg p.R431Q ESCA 11 67012683 67012683 + Silent SNP G G A TCGA-L5-A4OW-01A-11D-A28B-09 TCGA-L5-A4OW-11A-11D-A28E-09 g.chr11:67012683G>A c.1587G>A c.(1585-1587)aaG>aaA p.K529K GBMLGG 11 67012792 67012792 + Missense_Mutation SNP C C T TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr11:67012792C>T c.1696C>T c.(1696-1698)Cgg>Tgg p.R566W GBMLGG 11 67018104 67018104 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:67018104A>G c.2603A>G c.(2602-2604)gAc>gGc p.D868G HNSC 11 66888812 66888812 + Missense_Mutation SNP C C T TCGA-CX-7086-01A-11D-2078-08 TCGA-CX-7086-10D-01D-2078-08 g.chr11:66888812C>T c.25C>T c.(25-27)Cgt>Tgt p.R9C HNSC 11 66982819 66982819 + Missense_Mutation SNP C C G TCGA-WA-A7GZ-01A-11D-A34J-08 TCGA-WA-A7GZ-10A-01D-A34M-08 g.chr11:66982819C>G c.495C>G c.(493-495)ttC>ttG p.F165L HNSC 11 66983411 66983412 + Frame_Shift_Ins INS - - G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:66983411_66983412insG c.678_679insG c.(679-681)gggfs p.G227fs HNSC 11 66985207 66985207 + Silent SNP C C T TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr11:66985207C>T c.693C>T c.(691-693)ttC>ttT p.F231F HNSC 11 66985219 66985219 + Silent SNP C C T TCGA-BA-4074-01A-01D-1434-08 TCGA-BA-4074-10A-01D-1434-08 g.chr11:66985219C>T c.705C>T c.(703-705)ccC>ccT p.P235P HNSC 11 66986772 66986772 + Silent SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:66986772T>C c.855T>C c.(853-855)gcT>gcC p.A285A HNSC 11 67021746 67021746 + Missense_Mutation SNP C C T TCGA-CN-A499-01A-11D-A24D-08 TCGA-CN-A499-10A-01D-A24F-08 g.chr11:67021746C>T c.3164C>T c.(3163-3165)aCg>aTg p.T1055M KICH 11 67022407 67022407 + Missense_Mutation SNP A A T TCGA-KL-8335-01A-11D-2310-10 TCGA-KL-8335-11A-01D-2310-10 g.chr11:67022407A>T c.3370A>T c.(3370-3372)Atc>Ttc p.I1124F KIPAN 11 66999421 66999421 + Missense_Mutation SNP C C T TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr11:66999421C>T c.1469C>T c.(1468-1470)gCt>gTt p.A490V KIPAN 11 67017709 67017709 + Silent SNP G G A TCGA-CJ-4895-01A-01D-1373-10 TCGA-CJ-4895-11A-01D-1373-10 g.chr11:67017709G>A c.2208G>A c.(2206-2208)gtG>gtA p.V736V KIPAN 11 67017906 67017906 + Missense_Mutation SNP C C T TCGA-CJ-6033-01A-11D-1669-08 TCGA-CJ-6033-11A-01D-1669-08 g.chr11:67017906C>T c.2405C>T c.(2404-2406)aCg>aTg p.T802M KIPAN 11 67021798 67021798 + Missense_Mutation SNP T T G TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chr11:67021798T>G c.3216T>G c.(3214-3216)agT>agG p.S1072R KIPAN 11 67022407 67022407 + Missense_Mutation SNP A A T TCGA-KL-8335-01A-11D-2310-10 TCGA-KL-8335-11A-01D-2310-10 g.chr11:67022407A>T c.3370A>T c.(3370-3372)Atc>Ttc p.I1124F KIRC 11 66999421 66999421 + Missense_Mutation SNP C C T TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr11:66999421C>T c.1469C>T c.(1468-1470)gCt>gTt p.A490V KIRC 11 67017709 67017709 + Silent SNP G G A TCGA-CJ-4895-01A-01D-1373-10 TCGA-CJ-4895-11A-01D-1373-10 g.chr11:67017709G>A c.2208G>A c.(2206-2208)gtG>gtA p.V736V KIRC 11 67017906 67017906 + Missense_Mutation SNP C C T TCGA-CJ-6033-01A-11D-1669-08 TCGA-CJ-6033-11A-01D-1669-08 g.chr11:67017906C>T c.2405C>T c.(2404-2406)aCg>aTg p.T802M KIRC 11 67021798 67021798 + Missense_Mutation SNP T T G TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chr11:67021798T>G c.3216T>G c.(3214-3216)agT>agG p.S1072R LGG 11 67012792 67012792 + Missense_Mutation SNP C C T TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr11:67012792C>T c.1696C>T c.(1696-1698)Cgg>Tgg p.R566W LGG 11 67018104 67018104 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:67018104A>G c.2603A>G c.(2602-2604)gAc>gGc p.D868G LIHC 11 66975117 66975117 + Missense_Mutation SNP T T A TCGA-DD-A1EB-01A-11D-A12Z-10 TCGA-DD-A1EB-10A-01D-A12Z-10 g.chr11:66975117T>A c.444T>A c.(442-444)ttT>ttA p.F148L LIHC 11 66982895 66982895 + Missense_Mutation SNP A A T TCGA-BD-A3EP-01A-11D-A22F-10 TCGA-BD-A3EP-11A-12D-A22F-10 g.chr11:66982895A>T c.571A>T c.(571-573)Atg>Ttg p.M191L LIHC 11 66986855 66986855 + Missense_Mutation SNP A A G TCGA-DD-A1EB-01A-11D-A12Z-10 TCGA-DD-A1EB-10A-01D-A12Z-10 g.chr11:66986855A>G c.938A>G c.(937-939)aAc>aGc p.N313S LIHC 11 67015791 67015791 + Missense_Mutation SNP T T A TCGA-DD-AAW0-01A-11D-A40R-10 TCGA-DD-AAW0-10A-01D-A40U-10 g.chr11:67015791T>A c.2005T>A c.(2005-2007)Tgc>Agc p.C669S LIHC 11 67017960 67017960 + Missense_Mutation SNP A A G TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr11:67017960A>G c.2459A>G c.(2458-2460)cAg>cGg p.Q820R LIHC 11 67020287 67020287 + Missense_Mutation SNP T T C TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr11:67020287T>C c.2891T>C c.(2890-2892)aTc>aCc p.I964T LUAD 11 66948816 66948816 + Silent SNP G G T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr11:66948816G>T c.207G>T c.(205-207)cgG>cgT p.R69R LUAD 11 66985245 66985245 + Missense_Mutation SNP A A G TCGA-55-6969-01A-11D-1945-08 TCGA-55-6969-11A-01D-1945-08 g.chr11:66985245A>G c.731A>G c.(730-732)tAc>tGc p.Y244C LUAD 11 67013473 67013473 + Silent SNP A A T TCGA-44-6144-01A-11D-1753-08 TCGA-44-6144-10A-01D-1753-08 g.chr11:67013473A>T c.1851A>T c.(1849-1851)tcA>tcT p.S617S LUAD 11 67018026 67018026 + Missense_Mutation SNP C C T TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr11:67018026C>T c.2525C>T c.(2524-2526)gCc>gTc p.A842V LUAD 11 67018061 67018061 + Missense_Mutation SNP G G T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr11:67018061G>T c.2560G>T c.(2560-2562)Ggg>Tgg p.G854W LUAD 11 67018137 67018137 + Missense_Mutation SNP A A G TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr11:67018137A>G c.2636A>G c.(2635-2637)aAt>aGt p.N879S LUAD 11 67020928 67020928 + Silent SNP G G A TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr11:67020928G>A c.2937G>A c.(2935-2937)ctG>ctA p.L979L LUAD 11 67021837 67021837 + Silent SNP C C T TCGA-91-A4BD-01A-11D-A24D-08 TCGA-91-A4BD-10A-01D-A24F-08 g.chr11:67021837C>T c.3255C>T c.(3253-3255)ctC>ctT p.L1085L LUAD 11 67021866 67021866 + Missense_Mutation SNP C C G TCGA-05-4420-01A-01D-1265-08 TCGA-05-4420-10A-01D-1265-08 g.chr11:67021866C>G c.3284C>G c.(3283-3285)tCt>tGt p.S1095C LUAD 11 67021879 67021879 + Silent SNP C C G TCGA-78-7156-01A-11D-2036-08 TCGA-78-7156-10A-01D-2036-08 g.chr11:67021879C>G c.3297C>G c.(3295-3297)ctC>ctG p.L1099L LUSC 11 66947553 66947553 + Missense_Mutation SNP G G T TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr11:66947553G>T c.46G>T c.(46-48)Ggt>Tgt p.G16C LUSC 11 66983395 66983395 + Missense_Mutation SNP G G T TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr11:66983395G>T c.662G>T c.(661-663)tGg>tTg p.W221L LUSC 11 66995566 66995566 + Missense_Mutation SNP G G A TCGA-70-6723-01A-11D-1817-08 TCGA-70-6723-10A-01D-1817-08 g.chr11:66995566G>A c.1016G>A c.(1015-1017)cGc>cAc p.R339H LUSC 11 67017759 67017759 + Missense_Mutation SNP G G A TCGA-22-5482-01A-01D-1632-08 TCGA-22-5482-11A-01D-1632-08 g.chr11:67017759G>A c.2258G>A c.(2257-2259)cGc>cAc p.R753H OV 11 66983400 66983400 + Missense_Mutation SNP C C T TCGA-13-0889-01A-01W-0419-10 TCGA-13-0889-10A-01W-0419-10 g.chr11:66983400C>T c.667C>T c.(667-669)Cac>Tac p.H223Y OV 11 67017881 67017881 + Missense_Mutation SNP A A C TCGA-24-1417-01A-01W-0549-09 TCGA-24-1417-10A-01W-0549-09 g.chr11:67017881A>C c.2380A>C c.(2380-2382)Atc>Ctc p.I794L OV 11 67020275 67020275 + Missense_Mutation SNP G G A TCGA-24-0968-01A-01W-0484-10 TCGA-24-0968-10C-01W-0484-10 g.chr11:67020275G>A c.2879G>A c.(2878-2880)aGt>aAt p.S960N OV 11 67021790 67021790 + Missense_Mutation SNP G G A TCGA-61-1915-01A-01W-0639-09 TCGA-61-1915-11A-01W-0640-09 g.chr11:67021790G>A c.3208G>A c.(3208-3210)Gac>Aac p.D1070N OV 11 67022386 67022386 + Missense_Mutation SNP C C T TCGA-13-0760-01A-01W-0372-09 TCGA-13-0760-10A-01W-0372-09 g.chr11:67022386C>T c.3349C>T c.(3349-3351)Cgc>Tgc p.R1117C PAAD 11 66975059 66975059 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:66975059A>G c.386A>G c.(385-387)tAc>tGc p.Y129C PAAD 11 67012741 67012741 + Silent SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:67012741T>C c.1645T>C c.(1645-1647)Tta>Cta p.L549L PAAD 11 67018039 67018039 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:67018039G>A c.2538G>A c.(2536-2538)caG>caA p.Q846Q PAAD 11 67018079 67018081 + In_Frame_Del DEL GAG GAG - TCGA-FB-AAPZ-01A-11D-A40W-08 TCGA-FB-AAPZ-11A-11D-A40W-08 g.chr11:67018079_67018081delGAG c.2578_2580delGAG c.(2578-2580)gagdel p.E866del PAAD 11 67018079 67018081 + In_Frame_Del DEL GAG GAG - TCGA-FB-AAQ1-01A-12D-A40W-08 TCGA-FB-AAQ1-11A-11D-A40W-08 g.chr11:67018079_67018081delGAG c.2578_2580delGAG c.(2578-2580)gagdel p.E866del PAAD 11 67018079 67018081 + In_Frame_Del DEL GAG GAG - TCGA-IB-7652-01A-11D-2154-08 TCGA-IB-7652-10A-01D-2154-08 g.chr11:67018079_67018081delGAG c.2578_2580delGAG c.(2578-2580)gagdel p.E866del PAAD 11 67018079 67018081 + In_Frame_Del DEL GAG GAG - TCGA-YH-A8SY-01A-11D-A377-08 TCGA-YH-A8SY-10A-01D-A37A-08 g.chr11:67018079_67018081delGAG c.2578_2580delGAG c.(2578-2580)gagdel p.E866del PAAD 11 67018081 67018081 + Silent SNP G G A TCGA-2L-AAQM-01A-11D-A397-08 TCGA-2L-AAQM-11A-11D-A39A-08 g.chr11:67018081G>A c.2580G>A c.(2578-2580)gaG>gaA p.E860E PRAD 11 66985327 66985327 + Silent SNP G G A TCGA-J9-A8CL-01A-11D-A34U-08 TCGA-J9-A8CL-10A-01D-A34X-08 g.chr11:66985327G>A c.813G>A c.(811-813)aaG>aaA p.K271K PRAD 11 66999361 66999361 + Missense_Mutation SNP C C A TCGA-HC-8216-01A-11D-A29Q-08 TCGA-HC-8216-10A-01D-A29Q-08 g.chr11:66999361C>A c.1409C>A c.(1408-1410)tCt>tAt p.S470Y PRAD 11 67017956 67017956 + Missense_Mutation SNP C C A TCGA-HC-A4ZV-01A-11D-A26M-08 TCGA-HC-A4ZV-10A-01D-A26K-08 g.chr11:67017956C>A c.2455C>A c.(2455-2457)Ctg>Atg p.L819M SARC 11 67013488 67013488 + Silent SNP C C T TCGA-DX-A7ES-01A-31D-A38Z-09 TCGA-DX-A7ES-10A-01D-A38Z-09 g.chr11:67013488C>T c.1866C>T c.(1864-1866)ctC>ctT p.L622L SKCM 11 66948824 66948824 + Nonsense_Mutation SNP T T A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr11:66948824T>A c.215T>A c.(214-216)tTg>tAg p.L72* SKCM 11 66999061 66999061 + Missense_Mutation SNP C C T TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr11:66999061C>T c.1109C>T c.(1108-1110)tCt>tTt p.S370F SKCM 11 67012770 67012770 + Silent SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr11:67012770C>T c.1674C>T c.(1672-1674)tcC>tcT p.S558S SKCM 11 67012810 67012810 + Nonsense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:67012810C>T c.1714C>T c.(1714-1716)Cga>Tga p.R572* SKCM 11 67015803 67015803 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:67015803C>T c.2017C>T c.(2017-2019)Cca>Tca p.P673S SKCM 11 67017891 67017891 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:67017891C>T c.2390C>T c.(2389-2391)tCg>tTg p.S797L SKCM 11 67020215 67020215 + Missense_Mutation SNP C C T TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr11:67020215C>T c.2819C>T c.(2818-2820)gCc>gTc p.A940V SKCM 11 67020265 67020265 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr11:67020265C>T c.2869C>T c.(2869-2871)Ctt>Ttt p.L957F SKCM 11 67022482 67022482 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:67022482C>T c.3445C>T c.(3445-3447)Ctc>Ttc p.L1149F

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 11 67017821 67017821 single base substitution C T downstream_gene_variant BLCA-US 11 67017821 67017821 single base substitution C T exon_variant BLCA-US 11 67017821 67017821 single base substitution C T missense_variant R232W 694C>T BLCA-US 11 67017821 67017821 single base substitution C T missense_variant R335W 1003C>T BLCA-US 11 67017821 67017821 single base substitution C T missense_variant R774W 2320C>T BLCA-US 11 67017821 67017821 single base substitution C T splice_region_variant BLCA-US 11 67017821 67017821 single base substitution C T upstream_gene_variant BLCA-US 11 67021043 67021043 single base substitution C G 3_prime_UTR_variant BLCA-US 11 67021043 67021043 single base substitution C G downstream_gene_variant BLCA-US 11 67021043 67021043 single base substitution C G exon_variant BLCA-US 11 67021043 67021043 single base substitution C G missense_variant Q1018E 3052C>G BLCA-US 11 67021043 67021043 single base substitution C G missense_variant Q476E 1426C>G BLCA-US 11 67021043 67021043 single base substitution C G missense_variant Q579E 1735C>G BLCA-US 11 67021049 67021049 single base substitution C T 3_prime_UTR_variant BLCA-US 11 67021049 67021049 single base substitution C T downstream_gene_variant BLCA-US 11 67021049 67021049 single base substitution C T exon_variant BLCA-US 11 67021049 67021049 single base substitution C T missense_variant R1020W 3058C>T BLCA-US 11 67021049 67021049 single base substitution C T missense_variant R478W 1432C>T BLCA-US 11 67021049 67021049 single base substitution C T missense_variant R581W 1741C>T BLCA-US 11 67022406 67022406 single base substitution G A 3_prime_UTR_variant BLCA-US 11 67022406 67022406 single base substitution G A exon_variant BLCA-US 11 67022406 67022406 single base substitution G A synonymous_variant L1123L 3369G>A BLCA-US 11 67022406 67022406 single base substitution G A synonymous_variant L581L 1743G>A BLCA-US 11 67022406 67022406 single base substitution G A synonymous_variant L684L 2052G>A BRCA-EU 11 66882444 66882444 single base substitution G C upstream_gene_variant BRCA-EU 11 66883440 66883440 single base substitution C T upstream_gene_variant BRCA-EU 11 66884664 66884664 single base substitution C A upstream_gene_variant BRCA-EU 11 66885539 66885539 single base substitution G C upstream_gene_variant BRCA-EU 11 66885540 66885540 single base substitution G T upstream_gene_variant BRCA-EU 11 66887279 66887279 single base substitution G A 5_prime_UTR_variant BRCA-EU 11 66887279 66887279 single base substitution G A upstream_gene_variant BRCA-EU 11 66887536 66887536 single base substitution C T intron_variant BRCA-EU 11 66887742 66887742 single base substitution C T intron_variant BRCA-EU 11 66887784 66887784 single base substitution C T intron_variant BRCA-EU 11 66888898 66888898 single base substitution G A intron_variant BRCA-EU 11 66888973 66888973 single base substitution A G intron_variant BRCA-EU 11 66889252 66889252 single base substitution G A intron_variant BRCA-EU 11 66889711 66889711 insertion of <=200bp - T intron_variant BRCA-EU 11 66889817 66889817 single base substitution G A intron_variant BRCA-EU 11 66890177 66890177 single base substitution G C intron_variant BRCA-EU 11 66891713 66891713 single base substitution G A intron_variant BRCA-EU 11 66892920 66892920 single base substitution A C intron_variant BRCA-EU 11 66895345 66895345 single base substitution T A intron_variant BRCA-EU 11 66895383 66895383 single base substitution G T intron_variant BRCA-EU 11 66895739 66895739 single base substitution C G intron_variant BRCA-EU 11 66895819 66895819 single base substitution G A intron_variant BRCA-EU 11 66896189 66896189 single base substitution C T intron_variant BRCA-EU 11 66896321 66896321 single base substitution T C intron_variant BRCA-EU 11 66897715 66897715 single base substitution C G intron_variant BRCA-EU 11 66897717 66897717 single base substitution A C intron_variant BRCA-EU 11 66898688 66898688 single base substitution G C intron_variant BRCA-EU 11 66900000 66900000 single base substitution C T intron_variant BRCA-EU 11 66900373 66900373 insertion of <=200bp - T intron_variant BRCA-EU 11 66902552 66902552 single base substitution C T intron_variant BRCA-EU 11 66902656 66902656 single base substitution C T intron_variant BRCA-EU 11 66902764 66902764 single base substitution C G intron_variant BRCA-EU 11 66903074 66903074 single base substitution C T intron_variant BRCA-EU 11 66905385 66905385 single base substitution C T intron_variant BRCA-EU 11 66910467 66910467 single base substitution T A intron_variant BRCA-EU 11 66910609 66910609 single base substitution C T intron_variant BRCA-EU 11 66910772 66910772 single base substitution C T exon_variant BRCA-EU 11 66910772 66910772 single base substitution C T intron_variant BRCA-EU 11 66912228 66912228 single base substitution G C intron_variant BRCA-EU 11 66912270 66912270 single base substitution C T intron_variant BRCA-EU 11 66913149 66913149 single base substitution T C intron_variant BRCA-EU 11 66913946 66913946 single base substitution C G intron_variant BRCA-EU 11 66915489 66915489 single base substitution C G intron_variant BRCA-EU 11 66915635 66915635 single base substitution G C intron_variant BRCA-EU 11 66916666 66916666 single base substitution G A exon_variant BRCA-EU 11 66916666 66916666 single base substitution G A intron_variant BRCA-EU 11 66919667 66919667 single base substitution C T downstream_gene_variant BRCA-EU 11 66919667 66919667 single base substitution C T intron_variant BRCA-EU 11 66922489 66922489 single base substitution T A intron_variant BRCA-EU 11 66922634 66922634 single base substitution T A intron_variant BRCA-EU 11 66922958 66922958 single base substitution G A intron_variant BRCA-EU 11 66924356 66924356 single base substitution C G intron_variant BRCA-EU 11 66924374 66924374 single base substitution G A intron_variant BRCA-EU 11 66924560 66924560 single base substitution C T intron_variant BRCA-EU 11 66924715 66924715 single base substitution C T intron_variant BRCA-EU 11 66924864 66924864 single base substitution G C intron_variant BRCA-EU 11 66926214 66926214 single base substitution A G intron_variant BRCA-EU 11 66928243 66928243 insertion of <=200bp - A intron_variant BRCA-EU 11 66928400 66928400 single base substitution G A intron_variant BRCA-EU 11 66929827 66929827 single base substitution C T intron_variant BRCA-EU 11 66932961 66932961 single base substitution A G intron_variant BRCA-EU 11 66933010 66933010 single base substitution A T intron_variant BRCA-EU 11 66935496 66935496 single base substitution C A intron_variant BRCA-EU 11 66935502 66935503 deletion of <=200bp TT - intron_variant BRCA-EU 11 66935584 66935584 single base substitution G C intron_variant BRCA-EU 11 66935868 66935868 single base substitution T A intron_variant BRCA-EU 11 66935892 66935892 single base substitution T A intron_variant BRCA-EU 11 66938158 66938158 single base substitution A G intron_variant BRCA-EU 11 66938211 66938214 deletion of <=200bp TTCT - intron_variant BRCA-EU 11 66938218 66938218 single base substitution T G intron_variant BRCA-EU 11 66939409 66939409 single base substitution C G intron_variant BRCA-EU 11 66940210 66940210 single base substitution G A intron_variant BRCA-EU 11 66940309 66940309 single base substitution G T intron_variant BRCA-EU 11 66942312 66942312 single base substitution C G intron_variant BRCA-EU 11 66942728 66942728 single base substitution C T intron_variant BRCA-EU 11 66943063 66943063 single base substitution C T intron_variant BRCA-EU 11 66943451 66943451 single base substitution C T intron_variant BRCA-EU 11 66944374 66944374 insertion of <=200bp - G intron_variant BRCA-EU 11 66944494 66944513 deletion of <=200bp TGAGGTGGGCGGATCACCTG - intron_variant BRCA-EU 11 66945401 66945401 insertion of <=200bp - T intron_variant BRCA-EU 11 66947362 66947362 single base substitution A C intron_variant BRCA-EU 11 66950524 66950524 single base substitution C T downstream_gene_variant BRCA-EU 11 66950524 66950524 single base substitution C T intron_variant BRCA-EU 11 66950697 66950697 single base substitution C G downstream_gene_variant BRCA-EU 11 66950697 66950697 single base substitution C G intron_variant BRCA-EU 11 66952556 66952556 single base substitution C T downstream_gene_variant BRCA-EU 11 66952556 66952556 single base substitution C T intron_variant BRCA-EU 11 66953574 66953574 single base substitution A T intron_variant BRCA-EU 11 66955202 66955202 single base substitution G A intron_variant BRCA-EU 11 66955542 66955542 single base substitution G A intron_variant BRCA-EU 11 66958346 66958346 single base substitution T A intron_variant BRCA-EU 11 66959524 66959524 single base substitution C G intron_variant BRCA-EU 11 66961227 66961227 single base substitution G A intron_variant BRCA-EU 11 66962472 66962472 single base substitution G C intron_variant BRCA-EU 11 66965855 66965855 single base substitution T G intron_variant BRCA-EU 11 66966697 66966697 single base substitution C T intron_variant BRCA-EU 11 66966842 66966842 single base substitution C G intron_variant BRCA-EU 11 66967245 66967245 single base substitution C T intron_variant BRCA-EU 11 66967651 66967651 single base substitution G A intron_variant BRCA-EU 11 66968590 66968590 single base substitution G A intron_variant BRCA-EU 11 66968601 66968601 single base substitution C G intron_variant BRCA-EU 11 66970789 66970789 single base substitution T G intron_variant BRCA-EU 11 66970789 66970789 single base substitution T G upstream_gene_variant BRCA-EU 11 66971429 66971429 single base substitution G A intron_variant BRCA-EU 11 66971429 66971429 single base substitution G A upstream_gene_variant BRCA-EU 11 66973087 66973087 deletion of <=200bp T - intron_variant BRCA-EU 11 66973087 66973087 deletion of <=200bp T - upstream_gene_variant BRCA-EU 11 66974029 66974029 single base substitution G A intron_variant BRCA-EU 11 66974029 66974029 single base substitution G A upstream_gene_variant BRCA-EU 11 66974157 66974157 single base substitution G A intron_variant BRCA-EU 11 66974157 66974157 single base substitution G A upstream_gene_variant BRCA-EU 11 66974270 66974270 single base substitution C G intron_variant BRCA-EU 11 66974270 66974270 single base substitution C G upstream_gene_variant BRCA-EU 11 66974329 66974329 single base substitution G A intron_variant BRCA-EU 11 66974329 66974329 single base substitution G A upstream_gene_variant BRCA-EU 11 66976541 66976541 single base substitution A T intron_variant BRCA-EU 11 66977106 66977106 single base substitution G T intron_variant BRCA-EU 11 66977400 66977400 single base substitution A G intron_variant BRCA-EU 11 66979142 66979142 single base substitution C A intron_variant BRCA-EU 11 66979142 66979142 single base substitution C A upstream_gene_variant BRCA-EU 11 66980032 66980032 single base substitution C G intron_variant BRCA-EU 11 66980032 66980032 single base substitution C G upstream_gene_variant BRCA-EU 11 66980704 66980704 single base substitution C G intron_variant BRCA-EU 11 66980704 66980704 single base substitution C G upstream_gene_variant BRCA-EU 11 66981471 66981471 single base substitution C G intron_variant BRCA-EU 11 66981471 66981471 single base substitution C G upstream_gene_variant BRCA-EU 11 66981678 66981678 single base substitution A T intron_variant BRCA-EU 11 66981678 66981678 single base substitution A T upstream_gene_variant BRCA-EU 11 66983114 66983114 deletion of <=200bp A - exon_variant BRCA-EU 11 66983114 66983114 deletion of <=200bp A - intron_variant BRCA-EU 11 66983114 66983114 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 66983435 66983435 single base substitution G A downstream_gene_variant BRCA-EU 11 66983435 66983435 single base substitution G A intron_variant BRCA-EU 11 66983435 66983435 single base substitution G A upstream_gene_variant BRCA-EU 11 66983888 66983888 single base substitution A T downstream_gene_variant BRCA-EU 11 66983888 66983888 single base substitution A T intron_variant BRCA-EU 11 66983888 66983888 single base substitution A T upstream_gene_variant BRCA-EU 11 66984326 66984326 single base substitution G C downstream_gene_variant BRCA-EU 11 66984326 66984326 single base substitution G C intron_variant BRCA-EU 11 66984326 66984326 single base substitution G C upstream_gene_variant BRCA-EU 11 66985084 66985084 single base substitution G T downstream_gene_variant BRCA-EU 11 66985084 66985084 single base substitution G T exon_variant BRCA-EU 11 66985084 66985084 single base substitution G T intron_variant BRCA-EU 11 66986379 66986379 single base substitution C A downstream_gene_variant BRCA-EU 11 66986379 66986379 single base substitution C A intron_variant BRCA-EU 11 66986535 66986535 single base substitution G C downstream_gene_variant BRCA-EU 11 66986535 66986535 single base substitution G C intron_variant BRCA-EU 11 66986565 66986565 single base substitution G A downstream_gene_variant BRCA-EU 11 66986565 66986565 single base substitution G A intron_variant BRCA-EU 11 66986660 66986660 single base substitution G C downstream_gene_variant BRCA-EU 11 66986660 66986660 single base substitution G C intron_variant BRCA-EU 11 66986675 66986675 single base substitution T G downstream_gene_variant BRCA-EU 11 66986675 66986675 single base substitution T G intron_variant BRCA-EU 11 66988086 66988086 single base substitution C G downstream_gene_variant BRCA-EU 11 66988086 66988086 single base substitution C G intron_variant BRCA-EU 11 66989009 66989009 single base substitution G C downstream_gene_variant BRCA-EU 11 66989009 66989009 single base substitution G C intron_variant BRCA-EU 11 66990951 66990951 single base substitution G A downstream_gene_variant BRCA-EU 11 66990951 66990951 single base substitution G A intron_variant BRCA-EU 11 66991438 66991438 single base substitution G A downstream_gene_variant BRCA-EU 11 66991438 66991438 single base substitution G A intron_variant BRCA-EU 11 66992814 66992814 single base substitution A G intron_variant BRCA-EU 11 66994418 66994418 deletion of <=200bp A - intron_variant BRCA-EU 11 66994418 66994418 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 66994659 66994659 single base substitution C T intron_variant BRCA-EU 11 66994659 66994659 single base substitution C T upstream_gene_variant BRCA-EU 11 66994822 66994822 single base substitution C T intron_variant BRCA-EU 11 66994822 66994822 single base substitution C T upstream_gene_variant BRCA-EU 11 66995313 66995313 single base substitution A G intron_variant BRCA-EU 11 66995313 66995313 single base substitution A G upstream_gene_variant BRCA-EU 11 66997026 66997026 single base substitution C T intron_variant BRCA-EU 11 66997026 66997026 single base substitution C T upstream_gene_variant BRCA-EU 11 66997479 66997479 single base substitution C G intron_variant BRCA-EU 11 66997479 66997479 single base substitution C G upstream_gene_variant BRCA-EU 11 66998413 66998413 single base substitution A G intron_variant BRCA-EU 11 66998413 66998413 single base substitution A G upstream_gene_variant BRCA-EU 11 66998414 66998414 single base substitution G T intron_variant BRCA-EU 11 66998414 66998414 single base substitution G T upstream_gene_variant BRCA-EU 11 66998544 66998544 single base substitution C T intron_variant BRCA-EU 11 66998544 66998544 single base substitution C T upstream_gene_variant BRCA-EU 11 67000192 67000192 single base substitution T A intron_variant BRCA-EU 11 67000401 67000401 single base substitution G A intron_variant BRCA-EU 11 67001962 67001962 deletion of <=200bp T - intron_variant BRCA-EU 11 67002109 67002109 single base substitution G A intron_variant BRCA-EU 11 67002679 67002679 single base substitution C T intron_variant BRCA-EU 11 67002679 67002679 single base substitution C T upstream_gene_variant BRCA-EU 11 67003153 67003153 single base substitution C T intron_variant BRCA-EU 11 67003153 67003153 single base substitution C T upstream_gene_variant BRCA-EU 11 67005254 67005254 deletion of <=200bp A - intron_variant BRCA-EU 11 67005254 67005254 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 67006447 67006447 single base substitution C A intron_variant BRCA-EU 11 67006447 67006447 single base substitution C A upstream_gene_variant BRCA-EU 11 67007289 67007289 single base substitution T A intron_variant BRCA-EU 11 67007289 67007289 single base substitution T A upstream_gene_variant BRCA-EU 11 67007470 67007470 single base substitution C G intron_variant BRCA-EU 11 67007470 67007470 single base substitution C G upstream_gene_variant BRCA-EU 11 67007484 67007484 single base substitution C T intron_variant BRCA-EU 11 67007484 67007484 single base substitution C T upstream_gene_variant BRCA-EU 11 67008964 67008964 single base substitution G C intron_variant BRCA-EU 11 67008964 67008964 single base substitution G C upstream_gene_variant BRCA-EU 11 67009076 67009076 single base substitution C G intron_variant BRCA-EU 11 67009076 67009076 single base substitution C G upstream_gene_variant BRCA-EU 11 67009841 67009841 single base substitution C G intron_variant BRCA-EU 11 67009841 67009841 single base substitution C G upstream_gene_variant BRCA-EU 11 67013375 67013375 single base substitution C A downstream_gene_variant BRCA-EU 11 67013375 67013375 single base substitution C A exon_variant BRCA-EU 11 67013375 67013375 single base substitution C A intron_variant BRCA-EU 11 67014358 67014358 single base substitution T C downstream_gene_variant BRCA-EU 11 67014358 67014358 single base substitution T C intron_variant BRCA-EU 11 67015452 67015452 single base substitution C G downstream_gene_variant BRCA-EU 11 67015452 67015452 single base substitution C G intron_variant BRCA-EU 11 67015452 67015452 single base substitution C G upstream_gene_variant BRCA-EU 11 67015564 67015564 single base substitution C T downstream_gene_variant BRCA-EU 11 67015564 67015564 single base substitution C T intron_variant BRCA-EU 11 67015564 67015564 single base substitution C T upstream_gene_variant BRCA-EU 11 67019289 67019289 single base substitution G T downstream_gene_variant BRCA-EU 11 67019289 67019289 single base substitution G T intron_variant BRCA-EU 11 67019289 67019289 single base substitution G T upstream_gene_variant BRCA-EU 11 67019416 67019417 deletion of <=200bp CG - downstream_gene_variant BRCA-EU 11 67019416 67019417 deletion of <=200bp CG - intron_variant BRCA-EU 11 67019416 67019417 deletion of <=200bp CG - upstream_gene_variant BRCA-EU 11 67021197 67021197 single base substitution G C intron_variant BRCA-EU 11 67021316 67021316 single base substitution G A intron_variant BRCA-EU 11 67022460 67022460 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 67022460 67022460 single base substitution C G exon_variant BRCA-EU 11 67022460 67022460 single base substitution C G missense_variant I1141M 3423C>G BRCA-EU 11 67022460 67022460 single base substitution C G missense_variant I599M 1797C>G BRCA-EU 11 67022460 67022460 single base substitution C G missense_variant I702M 2106C>G BRCA-EU 11 67022542 67022542 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 67022542 67022542 single base substitution G C exon_variant BRCA-EU 11 67022714 67022714 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 67022714 67022714 single base substitution C G exon_variant BRCA-EU 11 67023098 67023098 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 67023098 67023098 single base substitution C G exon_variant BRCA-EU 11 67023495 67023495 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 67023495 67023495 single base substitution C G exon_variant BRCA-EU 11 67023645 67023645 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 67023645 67023645 single base substitution C G exon_variant BRCA-EU 11 67025417 67025417 single base substitution G T 3_prime_UTR_variant BRCA-EU 11 67025417 67025417 single base substitution G T downstream_gene_variant BRCA-EU 11 67025630 67025630 single base substitution C G downstream_gene_variant BRCA-EU 11 67025880 67025880 single base substitution G C downstream_gene_variant BRCA-EU 11 67025956 67025956 single base substitution G T downstream_gene_variant BRCA-EU 11 67025958 67025958 single base substitution G C downstream_gene_variant BRCA-EU 11 67028597 67028597 single base substitution G T downstream_gene_variant BRCA-EU 11 67028658 67028658 single base substitution C A downstream_gene_variant BRCA-EU 11 67029236 67029236 single base substitution G C downstream_gene_variant BRCA-EU 11 67029244 67029244 single base substitution G A downstream_gene_variant BRCA-EU 11 67029357 67029357 single base substitution G A downstream_gene_variant BRCA-EU 11 67029930 67029930 single base substitution C G downstream_gene_variant BRCA-EU 11 67029948 67029948 single base substitution C T downstream_gene_variant BRCA-FR 11 66884438 66884438 single base substitution G C upstream_gene_variant BRCA-FR 11 66889252 66889252 single base substitution G A intron_variant BRCA-FR 11 66895819 66895819 single base substitution G A intron_variant BRCA-FR 11 66896189 66896189 single base substitution C T intron_variant BRCA-FR 11 66898726 66898726 single base substitution T G intron_variant BRCA-FR 11 66900000 66900000 single base substitution C T intron_variant BRCA-FR 11 66905385 66905385 single base substitution C T intron_variant BRCA-FR 11 66909325 66909325 single base substitution C T intron_variant BRCA-FR 11 66909328 66909328 single base substitution C T intron_variant BRCA-FR 11 66914119 66914119 single base substitution A G intron_variant BRCA-FR 11 66922634 66922634 single base substitution T A intron_variant BRCA-FR 11 66924568 66924568 single base substitution A T intron_variant BRCA-FR 11 66924715 66924715 single base substitution C T intron_variant BRCA-FR 11 66935584 66935584 single base substitution G C intron_variant BRCA-FR 11 66937425 66937425 single base substitution C T intron_variant BRCA-FR 11 66942446 66942446 single base substitution C G intron_variant BRCA-FR 11 66943688 66943688 single base substitution C T intron_variant BRCA-FR 11 66950993 66950993 single base substitution C T downstream_gene_variant BRCA-FR 11 66950993 66950993 single base substitution C T intron_variant BRCA-FR 11 66955202 66955202 single base substitution G A intron_variant BRCA-FR 11 66962472 66962472 single base substitution G C intron_variant BRCA-FR 11 66967494 66967494 single base substitution C G intron_variant BRCA-FR 11 66974157 66974157 single base substitution G A intron_variant BRCA-FR 11 66974157 66974157 single base substitution G A upstream_gene_variant BRCA-FR 11 66985084 66985084 single base substitution G T downstream_gene_variant BRCA-FR 11 66985084 66985084 single base substitution G T exon_variant BRCA-FR 11 66985084 66985084 single base substitution G T intron_variant BRCA-FR 11 67001263 67001263 single base substitution G A intron_variant BRCA-FR 11 67002109 67002109 single base substitution G A intron_variant BRCA-FR 11 67003153 67003153 single base substitution C T intron_variant BRCA-FR 11 67003153 67003153 single base substitution C T upstream_gene_variant BRCA-FR 11 67006491 67006491 single base substitution G A intron_variant BRCA-FR 11 67006491 67006491 single base substitution G A upstream_gene_variant BRCA-FR 11 67007470 67007470 single base substitution C G intron_variant BRCA-FR 11 67007470 67007470 single base substitution C G upstream_gene_variant BRCA-FR 11 67010973 67010973 single base substitution T C intron_variant BRCA-FR 11 67010973 67010973 single base substitution T C upstream_gene_variant BRCA-FR 11 67012765 67012765 single base substitution G A downstream_gene_variant BRCA-FR 11 67012765 67012765 single base substitution G A exon_variant BRCA-FR 11 67012765 67012765 single base substitution G A missense_variant A118T 352G>A BRCA-FR 11 67012765 67012765 single base substitution G A missense_variant A15T 43G>A BRCA-FR 11 67012765 67012765 single base substitution G A missense_variant A557T 1669G>A BRCA-FR 11 67012765 67012765 single base substitution G A upstream_gene_variant BRCA-FR 11 67013375 67013375 single base substitution C A downstream_gene_variant BRCA-FR 11 67013375 67013375 single base substitution C A exon_variant BRCA-FR 11 67013375 67013375 single base substitution C A intron_variant BRCA-FR 11 67017609 67017609 single base substitution G A downstream_gene_variant BRCA-FR 11 67017609 67017609 single base substitution G A exon_variant BRCA-FR 11 67017609 67017609 single base substitution G A missense_variant R161Q 482G>A BRCA-FR 11 67017609 67017609 single base substitution G A missense_variant R264Q 791G>A BRCA-FR 11 67017609 67017609 single base substitution G A missense_variant R703Q 2108G>A BRCA-FR 11 67017609 67017609 single base substitution G A upstream_gene_variant BRCA-FR 11 67018888 67018888 single base substitution G A downstream_gene_variant BRCA-FR 11 67018888 67018888 single base substitution G A intron_variant BRCA-FR 11 67018888 67018888 single base substitution G A upstream_gene_variant BRCA-FR 11 67023495 67023495 single base substitution C G 3_prime_UTR_variant BRCA-FR 11 67023495 67023495 single base substitution C G exon_variant BRCA-FR 11 67025841 67025841 single base substitution G A downstream_gene_variant BRCA-FR 11 67025880 67025880 single base substitution G C downstream_gene_variant BRCA-FR 11 67025958 67025958 single base substitution G C downstream_gene_variant BRCA-FR 11 67028640 67028640 single base substitution C T downstream_gene_variant BRCA-FR 11 67029948 67029948 single base substitution C T downstream_gene_variant BRCA-UK 11 66895383 66895383 single base substitution G T intron_variant BRCA-UK 11 66903074 66903074 single base substitution C T intron_variant BRCA-UK 11 66912228 66912228 single base substitution G C intron_variant BRCA-UK 11 66965103 66965103 single base substitution G A intron_variant BRCA-UK 11 66974270 66974270 single base substitution C G intron_variant BRCA-UK 11 66974270 66974270 single base substitution C G upstream_gene_variant BRCA-UK 11 66988086 66988086 single base substitution C G downstream_gene_variant BRCA-UK 11 66988086 66988086 single base substitution C G intron_variant BRCA-UK 11 66990951 66990951 single base substitution G A downstream_gene_variant BRCA-UK 11 66990951 66990951 single base substitution G A intron_variant BRCA-UK 11 67001854 67001854 single base substitution C G intron_variant BRCA-UK 11 67008964 67008964 single base substitution G C intron_variant BRCA-UK 11 67008964 67008964 single base substitution G C upstream_gene_variant BRCA-UK 11 67019289 67019289 single base substitution G T downstream_gene_variant BRCA-UK 11 67019289 67019289 single base substitution G T intron_variant BRCA-UK 11 67019289 67019289 single base substitution G T upstream_gene_variant BRCA-UK 11 67020177 67020177 single base substitution G A downstream_gene_variant BRCA-UK 11 67020177 67020177 single base substitution G A exon_variant BRCA-UK 11 67020177 67020177 single base substitution G A missense_variant E777K 2329G>A BRCA-UK 11 67020177 67020177 single base substitution G A synonymous_variant K385K 1155G>A BRCA-UK 11 67020177 67020177 single base substitution G A synonymous_variant K488K 1464G>A BRCA-UK 11 67020177 67020177 single base substitution G A synonymous_variant K927K 2781G>A BRCA-UK 11 67025773 67025773 single base substitution G C downstream_gene_variant BRCA-US 11 66947566 66947566 single base substitution G A exon_variant BRCA-US 11 66947566 66947566 single base substitution G A missense_variant R20Q 59G>A BRCA-US 11 66985085 66985085 single base substitution A G downstream_gene_variant BRCA-US 11 66985085 66985085 single base substitution A G exon_variant BRCA-US 11 66985085 66985085 single base substitution A G intron_variant BRCA-US 11 66985342 66985342 single base substitution C T downstream_gene_variant BRCA-US 11 66985342 66985342 single base substitution C T exon_variant BRCA-US 11 66985342 66985342 single base substitution C T synonymous_variant F276F 828C>T BRCA-US 11 66995613 66995613 single base substitution C T exon_variant BRCA-US 11 66995613 66995613 single base substitution C T stop_gained Q355* 1063C>T BRCA-US 11 66995613 66995613 single base substitution C T upstream_gene_variant BRCA-US 11 66999259 66999259 single base substitution G A exon_variant BRCA-US 11 66999259 66999259 single base substitution G A missense_variant G436E 1307G>A BRCA-US 11 66999270 66999270 single base substitution G A exon_variant BRCA-US 11 66999270 66999270 single base substitution G A missense_variant D440N 1318G>A BRCA-US 11 67010479 67010479 single base substitution G T intron_variant BRCA-US 11 67010479 67010479 single base substitution G T splice_acceptor_variant BRCA-US 11 67010479 67010479 single base substitution G T upstream_gene_variant BRCA-US 11 67012672 67012672 single base substitution A C 5_prime_UTR_variant BRCA-US 11 67012672 67012672 single base substitution A C downstream_gene_variant BRCA-US 11 67012672 67012672 single base substitution A C exon_variant BRCA-US 11 67012672 67012672 single base substitution A C missense_variant T526P 1576A>C BRCA-US 11 67012672 67012672 single base substitution A C missense_variant T87P 259A>C BRCA-US 11 67012672 67012672 single base substitution A C upstream_gene_variant BRCA-US 11 67012699 67012699 single base substitution A G 5_prime_UTR_variant BRCA-US 11 67012699 67012699 single base substitution A G downstream_gene_variant BRCA-US 11 67012699 67012699 single base substitution A G exon_variant BRCA-US 11 67012699 67012699 single base substitution A G missense_variant I535V 1603A>G BRCA-US 11 67012699 67012699 single base substitution A G missense_variant I96V 286A>G BRCA-US 11 67012699 67012699 single base substitution A G upstream_gene_variant BRCA-US 11 67013375 67013375 single base substitution C T downstream_gene_variant BRCA-US 11 67013375 67013375 single base substitution C T exon_variant BRCA-US 11 67013375 67013375 single base substitution C T intron_variant BRCA-US 11 67017996 67017996 deletion of <=200bp C - downstream_gene_variant BRCA-US 11 67017996 67017996 deletion of <=200bp C - exon_variant BRCA-US 11 67017996 67017996 deletion of <=200bp C - frameshift_variant S290 BRCA-US 11 67017996 67017996 deletion of <=200bp C - frameshift_variant S393 BRCA-US 11 67017996 67017996 deletion of <=200bp C - frameshift_variant S832 BRCA-US 11 67017996 67017996 deletion of <=200bp C - intron_variant BRCA-US 11 67017996 67017996 deletion of <=200bp C - upstream_gene_variant BRCA-US 11 67018032 67018032 deletion of <=200bp C - downstream_gene_variant BRCA-US 11 67018032 67018032 deletion of <=200bp C - exon_variant BRCA-US 11 67018032 67018032 deletion of <=200bp C - frameshift_variant T302 BRCA-US 11 67018032 67018032 deletion of <=200bp C - frameshift_variant T405 BRCA-US 11 67018032 67018032 deletion of <=200bp C - frameshift_variant T844 BRCA-US 11 67018032 67018032 deletion of <=200bp C - intron_variant BRCA-US 11 67018032 67018032 deletion of <=200bp C - upstream_gene_variant BRCA-US 11 67020978 67020978 single base substitution G A 3_prime_UTR_variant BRCA-US 11 67020978 67020978 single base substitution G A downstream_gene_variant BRCA-US 11 67020978 67020978 single base substitution G A exon_variant BRCA-US 11 67020978 67020978 single base substitution G A missense_variant S454N 1361G>A BRCA-US 11 67020978 67020978 single base substitution G A missense_variant S557N 1670G>A BRCA-US 11 67020978 67020978 single base substitution G A missense_variant S996N 2987G>A BTCA-JP 11 66974983 66974983 single base substitution A G missense_variant S104G 310A>G BTCA-JP 11 66974983 66974983 single base substitution A G upstream_gene_variant BTCA-JP 11 67020914 67020914 single base substitution T A downstream_gene_variant BTCA-JP 11 67020914 67020914 single base substitution T A intron_variant BTCA-JP 11 67022354 67022354 single base substitution A C 3_prime_UTR_variant BTCA-JP 11 67022354 67022354 single base substitution A C exon_variant BTCA-JP 11 67022354 67022354 single base substitution A C missense_variant K1106T 3317A>C BTCA-JP 11 67022354 67022354 single base substitution A C missense_variant K564T 1691A>C BTCA-JP 11 67022354 67022354 single base substitution A C missense_variant K667T 2000A>C CESC-US 11 66975046 66975046 single base substitution C T exon_variant CESC-US 11 66975046 66975046 single base substitution C T stop_gained Q125* 373C>T CESC-US 11 66975046 66975046 single base substitution C T upstream_gene_variant CESC-US 11 66975079 66975079 single base substitution G A exon_variant CESC-US 11 66975079 66975079 single base substitution G A missense_variant E136K 406G>A CESC-US 11 66975147 66975147 single base substitution G A exon_variant CESC-US 11 66975147 66975147 single base substitution G A synonymous_variant Q158Q 474G>A CESC-US 11 66985142 66985142 single base substitution G C downstream_gene_variant CESC-US 11 66985142 66985142 single base substitution G C exon_variant CESC-US 11 66985142 66985142 single base substitution G C intron_variant CESC-US 11 66995615 66995615 single base substitution G C exon_variant CESC-US 11 66995615 66995615 single base substitution G C missense_variant Q355H 1065G>C CESC-US 11 66995615 66995615 single base substitution G C upstream_gene_variant CESC-US 11 66999107 66999107 single base substitution G C exon_variant CESC-US 11 66999107 66999107 single base substitution G C missense_variant L385F 1155G>C CESC-US 11 66999107 66999107 single base substitution G C upstream_gene_variant CESC-US 11 67017739 67017739 single base substitution C G downstream_gene_variant CESC-US 11 67017739 67017739 single base substitution C G exon_variant CESC-US 11 67017739 67017739 single base substitution C G missense_variant S204R 612C>G CESC-US 11 67017739 67017739 single base substitution C G missense_variant S307R 921C>G CESC-US 11 67017739 67017739 single base substitution C G missense_variant S746R 2238C>G CESC-US 11 67017739 67017739 single base substitution C G upstream_gene_variant CESC-US 11 67021785 67021785 single base substitution G A 3_prime_UTR_variant CESC-US 11 67021785 67021785 single base substitution G A exon_variant CESC-US 11 67021785 67021785 single base substitution G A missense_variant R1068Q 3203G>A CESC-US 11 67021785 67021785 single base substitution G A missense_variant R526Q 1577G>A CESC-US 11 67021785 67021785 single base substitution G A missense_variant R629Q 1886G>A CESC-US 11 67021879 67021879 single base substitution C A 3_prime_UTR_variant CESC-US 11 67021879 67021879 single base substitution C A exon_variant CESC-US 11 67021879 67021879 single base substitution C A synonymous_variant L1099L 3297C>A CESC-US 11 67021879 67021879 single base substitution C A synonymous_variant L557L 1671C>A CESC-US 11 67021879 67021879 single base substitution C A synonymous_variant L660L 1980C>A CESC-US 11 67022514 67022514 single base substitution G A 3_prime_UTR_variant CESC-US 11 67022514 67022514 single base substitution G A exon_variant CESC-US 11 67022514 67022514 single base substitution G A synonymous_variant Q1159Q 3477G>A CESC-US 11 67022514 67022514 single base substitution G A synonymous_variant Q617Q 1851G>A CESC-US 11 67022514 67022514 single base substitution G A synonymous_variant Q720Q 2160G>A CESC-US 11 67024771 67024771 single base substitution G A 3_prime_UTR_variant CESC-US 11 67024771 67024771 single base substitution G A downstream_gene_variant CESC-US 11 67024771 67024771 single base substitution G A exon_variant CLLE-ES 11 66883829 66883829 single base substitution G T upstream_gene_variant CLLE-ES 11 66892700 66892700 single base substitution A G intron_variant CLLE-ES 11 66894043 66894043 single base substitution G T intron_variant CLLE-ES 11 66920120 66920120 single base substitution T C downstream_gene_variant CLLE-ES 11 66920120 66920120 single base substitution T C intron_variant COAD-US 11 66975116 66975116 single base substitution T G exon_variant COAD-US 11 66975116 66975116 single base substitution T G missense_variant F148C 443T>G COAD-US 11 66975158 66975158 single base substitution C T missense_variant T162M 485C>T COAD-US 11 66975158 66975158 single base substitution C T splice_region_variant COAD-US 11 66986811 66986811 deletion of <=200bp T - downstream_gene_variant COAD-US 11 66986811 66986811 deletion of <=200bp T - exon_variant COAD-US 11 66986811 66986811 deletion of <=200bp T - frameshift_variant N298 COAD-US 11 66995629 66995629 single base substitution G A exon_variant COAD-US 11 66995629 66995629 single base substitution G A missense_variant S360N 1079G>A COAD-US 11 66995629 66995629 single base substitution G A upstream_gene_variant COAD-US 11 67013527 67013527 single base substitution T C downstream_gene_variant COAD-US 11 67013527 67013527 single base substitution T C exon_variant COAD-US 11 67013527 67013527 single base substitution T C synonymous_variant F196F 588T>C COAD-US 11 67013527 67013527 single base substitution T C synonymous_variant F635F 1905T>C COAD-US 11 67013527 67013527 single base substitution T C synonymous_variant F93F 279T>C COAD-US 11 67017699 67017699 single base substitution G A downstream_gene_variant COAD-US 11 67017699 67017699 single base substitution G A exon_variant COAD-US 11 67017699 67017699 single base substitution G A missense_variant R191Q 572G>A COAD-US 11 67017699 67017699 single base substitution G A missense_variant R294Q 881G>A COAD-US 11 67017699 67017699 single base substitution G A missense_variant R733Q 2198G>A COAD-US 11 67017699 67017699 single base substitution G A upstream_gene_variant COAD-US 11 67017963 67017963 single base substitution C T downstream_gene_variant COAD-US 11 67017963 67017963 single base substitution C T exon_variant COAD-US 11 67017963 67017963 single base substitution C T intron_variant COAD-US 11 67017963 67017963 single base substitution C T missense_variant A279V 836C>T COAD-US 11 67017963 67017963 single base substitution C T missense_variant A382V 1145C>T COAD-US 11 67017963 67017963 single base substitution C T missense_variant A821V 2462C>T COAD-US 11 67017963 67017963 single base substitution C T upstream_gene_variant COAD-US 11 67017996 67017996 deletion of <=200bp C - downstream_gene_variant COAD-US 11 67017996 67017996 deletion of <=200bp C - exon_variant COAD-US 11 67017996 67017996 deletion of <=200bp C - frameshift_variant S290 COAD-US 11 67017996 67017996 deletion of <=200bp C - frameshift_variant S393 COAD-US 11 67017996 67017996 deletion of <=200bp C - frameshift_variant S832 COAD-US 11 67017996 67017996 deletion of <=200bp C - intron_variant COAD-US 11 67017996 67017996 deletion of <=200bp C - upstream_gene_variant COAD-US 11 67018060 67018060 deletion of <=200bp G - downstream_gene_variant COAD-US 11 67018060 67018060 deletion of <=200bp G - exon_variant COAD-US 11 67018060 67018060 deletion of <=200bp G - frameshift_variant L311 COAD-US 11 67018060 67018060 deletion of <=200bp G - frameshift_variant L414 COAD-US 11 67018060 67018060 deletion of <=200bp G - frameshift_variant L853 COAD-US 11 67018060 67018060 deletion of <=200bp G - intron_variant COAD-US 11 67018060 67018060 deletion of <=200bp G - upstream_gene_variant COAD-US 11 67021715 67021715 single base substitution C T 3_prime_UTR_variant COAD-US 11 67021715 67021715 single base substitution C T exon_variant COAD-US 11 67021715 67021715 single base substitution C T missense_variant R1045W 3133C>T COAD-US 11 67021715 67021715 single base substitution C T missense_variant R503W 1507C>T COAD-US 11 67021715 67021715 single base substitution C T missense_variant R606W 1816C>T COCA-CN 11 66895174 66895174 single base substitution A T intron_variant COCA-CN 11 66923782 66923782 single base substitution G A intron_variant COCA-CN 11 66937858 66937858 single base substitution G T intron_variant COCA-CN 11 66937879 66937879 single base substitution C T intron_variant COCA-CN 11 66963742 66963742 single base substitution C A intron_variant COCA-CN 11 66968676 66968676 single base substitution T A intron_variant COCA-CN 11 66982928 66982928 single base substitution C T exon_variant COCA-CN 11 66982928 66982928 single base substitution C T intron_variant COCA-CN 11 66982928 66982928 single base substitution C T upstream_gene_variant COCA-CN 11 66983325 66983325 single base substitution A G downstream_gene_variant COCA-CN 11 66983325 66983325 single base substitution A G splice_acceptor_variant COCA-CN 11 66983325 66983325 single base substitution A G upstream_gene_variant COCA-CN 11 66983537 66983537 single base substitution G A downstream_gene_variant COCA-CN 11 66983537 66983537 single base substitution G A intron_variant COCA-CN 11 66983537 66983537 single base substitution G A upstream_gene_variant COCA-CN 11 67004926 67004926 single base substitution T C intron_variant COCA-CN 11 67004926 67004926 single base substitution T C upstream_gene_variant COCA-CN 11 67004929 67004929 single base substitution C T intron_variant COCA-CN 11 67004929 67004929 single base substitution C T upstream_gene_variant COCA-CN 11 67012777 67012777 single base substitution G A downstream_gene_variant COCA-CN 11 67012777 67012777 single base substitution G A exon_variant COCA-CN 11 67012777 67012777 single base substitution G A missense_variant V122M 364G>A COCA-CN 11 67012777 67012777 single base substitution G A missense_variant V19M 55G>A COCA-CN 11 67012777 67012777 single base substitution G A missense_variant V561M 1681G>A COCA-CN 11 67012777 67012777 single base substitution G A upstream_gene_variant COCA-CN 11 67013435 67013435 single base substitution T C downstream_gene_variant COCA-CN 11 67013435 67013435 single base substitution T C exon_variant COCA-CN 11 67013435 67013435 single base substitution T C intron_variant COCA-CN 11 67015779 67015779 single base substitution G T downstream_gene_variant COCA-CN 11 67015779 67015779 single base substitution G T exon_variant COCA-CN 11 67015779 67015779 single base substitution G T stop_gained E123* 367G>T COCA-CN 11 67015779 67015779 single base substitution G T stop_gained E226* 676G>T COCA-CN 11 67015779 67015779 single base substitution G T stop_gained E665* 1993G>T COCA-CN 11 67015779 67015779 single base substitution G T upstream_gene_variant COCA-CN 11 67017781 67017781 single base substitution G T downstream_gene_variant COCA-CN 11 67017781 67017781 single base substitution G T exon_variant COCA-CN 11 67017781 67017781 single base substitution G T synonymous_variant R218R 654G>T COCA-CN 11 67017781 67017781 single base substitution G T synonymous_variant R321R 963G>T COCA-CN 11 67017781 67017781 single base substitution G T synonymous_variant R760R 2280G>T COCA-CN 11 67017781 67017781 single base substitution G T upstream_gene_variant EOPC-DE 11 66907949 66907949 single base substitution G A intron_variant EOPC-DE 11 66908988 66908988 single base substitution A G intron_variant EOPC-DE 11 66923329 66923329 single base substitution C T intron_variant EOPC-DE 11 67006265 67006265 single base substitution C G intron_variant EOPC-DE 11 67006265 67006265 single base substitution C G upstream_gene_variant ESAD-UK 11 66883501 66883501 single base substitution C T upstream_gene_variant ESAD-UK 11 66885250 66885250 insertion of <=200bp - AGC upstream_gene_variant ESAD-UK 11 66886038 66886038 single base substitution C T upstream_gene_variant ESAD-UK 11 66889256 66889256 single base substitution G A intron_variant ESAD-UK 11 66890112 66890112 single base substitution A T intron_variant ESAD-UK 11 66890775 66890775 single base substitution G T intron_variant ESAD-UK 11 66892518 66892518 single base substitution G T intron_variant ESAD-UK 11 66892899 66892899 single base substitution G A intron_variant ESAD-UK 11 66895542 66895542 single base substitution A G intron_variant ESAD-UK 11 66896555 66896555 deletion of <=200bp A - intron_variant ESAD-UK 11 66896702 66896702 single base substitution C G intron_variant ESAD-UK 11 66899825 66899825 single base substitution G T intron_variant ESAD-UK 11 66905112 66905112 single base substitution A C intron_variant ESAD-UK 11 66905307 66905307 single base substitution C T intron_variant ESAD-UK 11 66907657 66907657 single base substitution C T intron_variant ESAD-UK 11 66909496 66909496 single base substitution T A intron_variant ESAD-UK 11 66910380 66910380 single base substitution T G intron_variant ESAD-UK 11 66910789 66910789 single base substitution T G exon_variant ESAD-UK 11 66910789 66910789 single base substitution T G intron_variant ESAD-UK 11 66911775 66911775 single base substitution G T intron_variant ESAD-UK 11 66915415 66915415 single base substitution G A intron_variant ESAD-UK 11 66917360 66917360 single base substitution T G downstream_gene_variant ESAD-UK 11 66917360 66917360 single base substitution T G intron_variant ESAD-UK 11 66917572 66917572 single base substitution G T downstream_gene_variant ESAD-UK 11 66917572 66917572 single base substitution G T intron_variant ESAD-UK 11 66918250 66918250 single base substitution C T downstream_gene_variant ESAD-UK 11 66918250 66918250 single base substitution C T intron_variant ESAD-UK 11 66919186 66919186 single base substitution G A downstream_gene_variant ESAD-UK 11 66919186 66919186 single base substitution G A intron_variant ESAD-UK 11 66920036 66920036 single base substitution G A downstream_gene_variant ESAD-UK 11 66920036 66920036 single base substitution G A intron_variant ESAD-UK 11 66921470 66921470 single base substitution G A downstream_gene_variant ESAD-UK 11 66921470 66921470 single base substitution G A intron_variant ESAD-UK 11 66921916 66921916 insertion of <=200bp - TTCC intron_variant ESAD-UK 11 66922618 66922618 single base substitution T G intron_variant ESAD-UK 11 66925509 66925509 single base substitution C T intron_variant ESAD-UK 11 66929359 66929359 single base substitution T G intron_variant ESAD-UK 11 66930120 66930120 single base substitution G A intron_variant ESAD-UK 11 66932249 66932249 single base substitution T G intron_variant ESAD-UK 11 66933010 66933010 single base substitution A G intron_variant ESAD-UK 11 66934933 66934933 single base substitution C T intron_variant ESAD-UK 11 66935171 66935171 single base substitution A G intron_variant ESAD-UK 11 66935903 66935903 single base substitution T C intron_variant ESAD-UK 11 66936919 66936919 single base substitution C T intron_variant ESAD-UK 11 66944062 66944062 single base substitution C G intron_variant ESAD-UK 11 66946784 66946784 single base substitution G A intron_variant ESAD-UK 11 66954879 66954879 single base substitution C T intron_variant ESAD-UK 11 66956060 66956060 single base substitution G C intron_variant ESAD-UK 11 66956360 66956360 single base substitution A T intron_variant ESAD-UK 11 66956528 66956528 single base substitution C A intron_variant ESAD-UK 11 66958228 66958228 single base substitution T A intron_variant ESAD-UK 11 66958570 66958570 single base substitution A G intron_variant ESAD-UK 11 66958786 66958786 single base substitution G C intron_variant ESAD-UK 11 66964281 66964281 single base substitution G T intron_variant ESAD-UK 11 66964792 66964792 single base substitution G A intron_variant ESAD-UK 11 66967248 66967248 single base substitution T C intron_variant ESAD-UK 11 66970337 66970337 single base substitution G A intron_variant ESAD-UK 11 66970337 66970337 single base substitution G A upstream_gene_variant ESAD-UK 11 66972048 66972048 single base substitution C T intron_variant ESAD-UK 11 66972048 66972048 single base substitution C T upstream_gene_variant ESAD-UK 11 66972051 66972051 single base substitution C T intron_variant ESAD-UK 11 66972051 66972051 single base substitution C T upstream_gene_variant ESAD-UK 11 66973835 66973835 single base substitution G A intron_variant ESAD-UK 11 66973835 66973835 single base substitution G A upstream_gene_variant ESAD-UK 11 66977063 66977063 single base substitution C T intron_variant ESAD-UK 11 66977135 66977135 single base substitution G A intron_variant ESAD-UK 11 66977365 66977365 single base substitution C G intron_variant ESAD-UK 11 66979337 66979337 single base substitution A G intron_variant ESAD-UK 11 66979337 66979337 single base substitution A G upstream_gene_variant ESAD-UK 11 66981099 66981099 single base substitution G A intron_variant ESAD-UK 11 66981099 66981099 single base substitution G A upstream_gene_variant ESAD-UK 11 66981745 66981745 single base substitution G A intron_variant ESAD-UK 11 66981745 66981745 single base substitution G A upstream_gene_variant ESAD-UK 11 66982112 66982112 deletion of <=200bp T - intron_variant ESAD-UK 11 66982112 66982112 deletion of <=200bp T - upstream_gene_variant ESAD-UK 11 66982195 66982195 deletion of <=200bp G - intron_variant ESAD-UK 11 66982195 66982195 deletion of <=200bp G - upstream_gene_variant ESAD-UK 11 66982394 66982394 insertion of <=200bp - C intron_variant ESAD-UK 11 66982394 66982394 insertion of <=200bp - C upstream_gene_variant ESAD-UK 11 66982469 66982469 single base substitution C T intron_variant ESAD-UK 11 66982469 66982469 single base substitution C T upstream_gene_variant ESAD-UK 11 66982522 66982522 single base substitution G C intron_variant ESAD-UK 11 66982522 66982522 single base substitution G C upstream_gene_variant ESAD-UK 11 66982995 66982995 single base substitution G A exon_variant ESAD-UK 11 66982995 66982995 single base substitution G A intron_variant ESAD-UK 11 66982995 66982995 single base substitution G A upstream_gene_variant ESAD-UK 11 66983147 66983147 single base substitution A G downstream_gene_variant ESAD-UK 11 66983147 66983147 single base substitution A G intron_variant ESAD-UK 11 66983147 66983147 single base substitution A G upstream_gene_variant ESAD-UK 11 66983768 66983768 single base substitution G A downstream_gene_variant ESAD-UK 11 66983768 66983768 single base substitution G A intron_variant ESAD-UK 11 66983768 66983768 single base substitution G A upstream_gene_variant ESAD-UK 11 66984061 66984061 single base substitution A G downstream_gene_variant ESAD-UK 11 66984061 66984061 single base substitution A G intron_variant ESAD-UK 11 66984061 66984061 single base substitution A G upstream_gene_variant ESAD-UK 11 66984117 66984117 single base substitution C T downstream_gene_variant ESAD-UK 11 66984117 66984117 single base substitution C T intron_variant ESAD-UK 11 66984117 66984117 single base substitution C T upstream_gene_variant ESAD-UK 11 66985841 66985841 single base substitution C T downstream_gene_variant ESAD-UK 11 66985841 66985841 single base substitution C T intron_variant ESAD-UK 11 66986387 66986387 single base substitution C T downstream_gene_variant ESAD-UK 11 66986387 66986387 single base substitution C T intron_variant ESAD-UK 11 66987411 66987411 single base substitution T A downstream_gene_variant ESAD-UK 11 66987411 66987411 single base substitution T A intron_variant ESAD-UK 11 66988215 66988215 single base substitution A G downstream_gene_variant ESAD-UK 11 66988215 66988215 single base substitution A G intron_variant ESAD-UK 11 66993665 66993665 single base substitution T A intron_variant ESAD-UK 11 66994389 66994389 single base substitution G A intron_variant ESAD-UK 11 66994389 66994389 single base substitution G A upstream_gene_variant ESAD-UK 11 66995229 66995229 single base substitution G T intron_variant ESAD-UK 11 66995229 66995229 single base substitution G T upstream_gene_variant ESAD-UK 11 66995477 66995477 single base substitution G A intron_variant ESAD-UK 11 66995477 66995477 single base substitution G A upstream_gene_variant ESAD-UK 11 66995900 66995900 single base substitution C T intron_variant ESAD-UK 11 66995900 66995900 single base substitution C T upstream_gene_variant ESAD-UK 11 66997727 66997727 single base substitution A C intron_variant ESAD-UK 11 66997727 66997727 single base substitution A C upstream_gene_variant ESAD-UK 11 66998129 66998129 single base substitution A C intron_variant ESAD-UK 11 66998129 66998129 single base substitution A C upstream_gene_variant ESAD-UK 11 66999565 66999565 single base substitution T C intron_variant ESAD-UK 11 67000326 67000326 single base substitution G A intron_variant ESAD-UK 11 67001521 67001521 single base substitution C T intron_variant ESAD-UK 11 67009897 67009897 single base substitution G C intron_variant ESAD-UK 11 67009897 67009897 single base substitution G C upstream_gene_variant ESAD-UK 11 67011159 67011159 single base substitution G A exon_variant ESAD-UK 11 67011159 67011159 single base substitution G A intron_variant ESAD-UK 11 67011159 67011159 single base substitution G A upstream_gene_variant ESAD-UK 11 67012569 67012569 single base substitution C T downstream_gene_variant ESAD-UK 11 67012569 67012569 single base substitution C T exon_variant ESAD-UK 11 67012569 67012569 single base substitution C T intron_variant ESAD-UK 11 67012569 67012569 single base substitution C T upstream_gene_variant ESAD-UK 11 67018060 67018060 deletion of <=200bp G - downstream_gene_variant ESAD-UK 11 67018060 67018060 deletion of <=200bp G - exon_variant ESAD-UK 11 67018060 67018060 deletion of <=200bp G - frameshift_variant L311 ESAD-UK 11 67018060 67018060 deletion of <=200bp G - frameshift_variant L414 ESAD-UK 11 67018060 67018060 deletion of <=200bp G - frameshift_variant L853 ESAD-UK 11 67018060 67018060 deletion of <=200bp G - intron_variant ESAD-UK 11 67018060 67018060 deletion of <=200bp G - upstream_gene_variant ESAD-UK 11 67018137 67018137 single base substitution A T downstream_gene_variant ESAD-UK 11 67018137 67018137 single base substitution A T exon_variant ESAD-UK 11 67018137 67018137 single base substitution A T intron_variant ESAD-UK 11 67018137 67018137 single base substitution A T missense_variant N337I 1010A>T ESAD-UK 11 67018137 67018137 single base substitution A T missense_variant N440I 1319A>T ESAD-UK 11 67018137 67018137 single base substitution A T missense_variant N879I 2636A>T ESAD-UK 11 67018137 67018137 single base substitution A T upstream_gene_variant ESAD-UK 11 67019472 67019472 single base substitution A G downstream_gene_variant ESAD-UK 11 67019472 67019472 single base substitution A G intron_variant ESAD-UK 11 67019472 67019472 single base substitution A G upstream_gene_variant ESAD-UK 11 67019947 67019947 single base substitution T C downstream_gene_variant ESAD-UK 11 67019947 67019947 single base substitution T C exon_variant ESAD-UK 11 67019947 67019947 single base substitution T C intron_variant ESAD-UK 11 67021062 67021062 single base substitution C T 3_prime_UTR_variant ESAD-UK 11 67021062 67021062 single base substitution C T downstream_gene_variant ESAD-UK 11 67021062 67021062 single base substitution C T exon_variant ESAD-UK 11 67021062 67021062 single base substitution C T missense_variant T1024I 3071C>T ESAD-UK 11 67021062 67021062 single base substitution C T missense_variant T482I 1445C>T ESAD-UK 11 67021062 67021062 single base substitution C T missense_variant T585I 1754C>T ESAD-UK 11 67022637 67022637 single base substitution C G 3_prime_UTR_variant ESAD-UK 11 67022637 67022637 single base substitution C G exon_variant ESAD-UK 11 67023202 67023202 single base substitution A G 3_prime_UTR_variant ESAD-UK 11 67023202 67023202 single base substitution A G exon_variant ESAD-UK 11 67023638 67023638 single base substitution C T 3_prime_UTR_variant ESAD-UK 11 67023638 67023638 single base substitution C T exon_variant ESAD-UK 11 67023792 67023792 single base substitution C G 3_prime_UTR_variant ESAD-UK 11 67023792 67023792 single base substitution C G exon_variant ESAD-UK 11 67028277 67028277 single base substitution G C downstream_gene_variant ESAD-UK 11 67029664 67029664 single base substitution C A downstream_gene_variant ESCA-CN 11 66975111 66975111 single base substitution C T exon_variant ESCA-CN 11 66975111 66975111 single base substitution C T synonymous_variant L146L 438C>T ESCA-CN 11 67022457 67022457 single base substitution C T 3_prime_UTR_variant ESCA-CN 11 67022457 67022457 single base substitution C T exon_variant ESCA-CN 11 67022457 67022457 single base substitution C T synonymous_variant F1140F 3420C>T ESCA-CN 11 67022457 67022457 single base substitution C T synonymous_variant F598F 1794C>T ESCA-CN 11 67022457 67022457 single base substitution C T synonymous_variant F701F 2103C>T KIRC-US 11 67017709 67017709 single base substitution G A downstream_gene_variant KIRC-US 11 67017709 67017709 single base substitution G A exon_variant KIRC-US 11 67017709 67017709 single base substitution G A synonymous_variant V194V 582G>A KIRC-US 11 67017709 67017709 single base substitution G A synonymous_variant V297V 891G>A KIRC-US 11 67017709 67017709 single base substitution G A synonymous_variant V736V 2208G>A KIRC-US 11 67017709 67017709 single base substitution G A upstream_gene_variant KIRC-US 11 67017906 67017906 single base substitution C T downstream_gene_variant KIRC-US 11 67017906 67017906 single base substitution C T exon_variant KIRC-US 11 67017906 67017906 single base substitution C T intron_variant KIRC-US 11 67017906 67017906 single base substitution C T missense_variant T260M 779C>T KIRC-US 11 67017906 67017906 single base substitution C T missense_variant T363M 1088C>T KIRC-US 11 67017906 67017906 single base substitution C T missense_variant T802M 2405C>T KIRC-US 11 67017906 67017906 single base substitution C T upstream_gene_variant KIRC-US 11 67021798 67021798 single base substitution T G 3_prime_UTR_variant KIRC-US 11 67021798 67021798 single base substitution T G exon_variant KIRC-US 11 67021798 67021798 single base substitution T G missense_variant S1072R 3216T>G KIRC-US 11 67021798 67021798 single base substitution T G missense_variant S530R 1590T>G KIRC-US 11 67021798 67021798 single base substitution T G missense_variant S633R 1899T>G LAML-KR 11 66891367 66891367 single base substitution C T intron_variant LAML-KR 11 66901142 66901142 single base substitution G A intron_variant LAML-KR 11 66901149 66901149 single base substitution C G intron_variant LAML-KR 11 66963425 66963425 single base substitution A G intron_variant LAML-KR 11 66991955 66991955 single base substitution G T downstream_gene_variant LAML-KR 11 66991955 66991955 single base substitution G T intron_variant LGG-US 11 67012792 67012792 single base substitution C T downstream_gene_variant LGG-US 11 67012792 67012792 single base substitution C T exon_variant LGG-US 11 67012792 67012792 single base substitution C T missense_variant R127W 379C>T LGG-US 11 67012792 67012792 single base substitution C T missense_variant R24W 70C>T LGG-US 11 67012792 67012792 single base substitution C T missense_variant R566W 1696C>T LGG-US 11 67012792 67012792 single base substitution C T upstream_gene_variant LICA-CN 11 66947556 66947556 single base substitution A G exon_variant LICA-CN 11 66947556 66947556 single base substitution A G missense_variant T17A 49A>G LICA-CN 11 66995607 66995607 single base substitution G T exon_variant LICA-CN 11 66995607 66995607 single base substitution G T stop_gained E353* 1057G>T LICA-CN 11 66995607 66995607 single base substitution G T upstream_gene_variant LICA-CN 11 66999329 66999329 single base substitution A C exon_variant LICA-CN 11 66999329 66999329 single base substitution A C missense_variant E459D 1377A>C LICA-FR 11 66888762 66888762 single base substitution C G 5_prime_UTR_variant LICA-FR 11 66888762 66888762 single base substitution C G exon_variant LICA-FR 11 66893696 66893696 single base substitution A T intron_variant LICA-FR 11 66922461 66922461 single base substitution A G intron_variant LICA-FR 11 66924190 66924191 deletion of <=200bp AA - intron_variant LICA-FR 11 66925659 66925659 single base substitution A G intron_variant LICA-FR 11 66935998 66935998 insertion of <=200bp - GTCTTGTATGAATTATAATACACACACACACACACACACA intron_variant LICA-FR 11 66958954 66958954 single base substitution A T intron_variant LICA-FR 11 66966181 66966181 deletion of <=200bp A - intron_variant LICA-FR 11 66973164 66973164 single base substitution G T intron_variant LICA-FR 11 66973164 66973164 single base substitution G T upstream_gene_variant LICA-FR 11 66983419 66983419 single base substitution A C downstream_gene_variant LICA-FR 11 66983419 66983419 single base substitution A C missense_variant K229T 686A>C LICA-FR 11 66983419 66983419 single base substitution A C splice_region_variant LICA-FR 11 66983419 66983419 single base substitution A C upstream_gene_variant LICA-FR 11 66989551 66989551 single base substitution A T downstream_gene_variant LICA-FR 11 66989551 66989551 single base substitution A T intron_variant LICA-FR 11 67004799 67004799 single base substitution C G intron_variant LICA-FR 11 67004799 67004799 single base substitution C G upstream_gene_variant LICA-FR 11 67006900 67006900 single base substitution A G intron_variant LICA-FR 11 67006900 67006900 single base substitution A G upstream_gene_variant LICA-FR 11 67012659 67012659 single base substitution G A downstream_gene_variant LICA-FR 11 67012659 67012659 single base substitution G A exon_variant LICA-FR 11 67012659 67012659 single base substitution G A splice_acceptor_variant LICA-FR 11 67012659 67012659 single base substitution G A upstream_gene_variant LICA-FR 11 67017626 67017626 single base substitution G T downstream_gene_variant LICA-FR 11 67017626 67017626 single base substitution G T exon_variant LICA-FR 11 67017626 67017626 single base substitution G T missense_variant D167Y 499G>T LICA-FR 11 67017626 67017626 single base substitution G T missense_variant D270Y 808G>T LICA-FR 11 67017626 67017626 single base substitution G T missense_variant D709Y 2125G>T LICA-FR 11 67017626 67017626 single base substitution G T upstream_gene_variant LIHC-US 11 66975111 66975111 single base substitution C A exon_variant LIHC-US 11 66975111 66975111 single base substitution C A synonymous_variant L146L 438C>A LIHC-US 11 66975117 66975117 single base substitution T A exon_variant LIHC-US 11 66975117 66975117 single base substitution T A missense_variant F148L 444T>A LIHC-US 11 66982895 66982895 single base substitution A T exon_variant LIHC-US 11 66982895 66982895 single base substitution A T missense_variant M191L 571A>T LIHC-US 11 66982895 66982895 single base substitution A T upstream_gene_variant LIHC-US 11 66986855 66986855 single base substitution A G downstream_gene_variant LIHC-US 11 66986855 66986855 single base substitution A G exon_variant LIHC-US 11 66986855 66986855 single base substitution A G missense_variant N313S 938A>G LIHC-US 11 66999328 66999328 single base substitution A G exon_variant LIHC-US 11 66999328 66999328 single base substitution A G missense_variant E459G 1376A>G LINC-JP 11 66882498 66882498 single base substitution T C upstream_gene_variant LINC-JP 11 66892173 66892173 deletion of <=200bp T - intron_variant LINC-JP 11 66892658 66892658 single base substitution C T intron_variant LINC-JP 11 66900592 66900592 single base substitution G A intron_variant LINC-JP 11 66927606 66927606 single base substitution G T intron_variant LINC-JP 11 66948676 66948676 single base substitution A G downstream_gene_variant LINC-JP 11 66948676 66948676 single base substitution A G intron_variant LINC-JP 11 66950302 66950302 single base substitution C T downstream_gene_variant LINC-JP 11 66950302 66950302 single base substitution C T intron_variant LINC-JP 11 66968066 66968066 single base substitution T G intron_variant LINC-JP 11 66968844 66968844 single base substitution G C intron_variant LINC-JP 11 66969976 66969976 single base substitution G C intron_variant LINC-JP 11 66970519 66970519 single base substitution A C intron_variant LINC-JP 11 66970519 66970519 single base substitution A C upstream_gene_variant LINC-JP 11 66972994 66972994 single base substitution G C intron_variant LINC-JP 11 66972994 66972994 single base substitution G C upstream_gene_variant LINC-JP 11 66980521 66980521 single base substitution A C intron_variant LINC-JP 11 66980521 66980521 single base substitution A C upstream_gene_variant LINC-JP 11 66988490 66988490 deletion of <=200bp A - downstream_gene_variant LINC-JP 11 66988490 66988490 deletion of <=200bp A - intron_variant LINC-JP 11 66990331 66990331 single base substitution A G downstream_gene_variant LINC-JP 11 66990331 66990331 single base substitution A G intron_variant LINC-JP 11 66994354 66994354 single base substitution T C intron_variant LINC-JP 11 66994354 66994354 single base substitution T C upstream_gene_variant LINC-JP 11 66995477 66995477 single base substitution G A intron_variant LINC-JP 11 66995477 66995477 single base substitution G A upstream_gene_variant LINC-JP 11 66996175 66996175 single base substitution G A intron_variant LINC-JP 11 66996175 66996175 single base substitution G A upstream_gene_variant LINC-JP 11 66999491 66999491 single base substitution A G intron_variant LINC-JP 11 67000118 67000118 insertion of <=200bp - T intron_variant LINC-JP 11 67003726 67003726 single base substitution T A intron_variant LINC-JP 11 67003726 67003726 single base substitution T A upstream_gene_variant LINC-JP 11 67009820 67009820 single base substitution A G intron_variant LINC-JP 11 67009820 67009820 single base substitution A G upstream_gene_variant LINC-JP 11 67015879 67015879 single base substitution G A downstream_gene_variant LINC-JP 11 67015879 67015879 single base substitution G A intron_variant LINC-JP 11 67015879 67015879 single base substitution G A upstream_gene_variant LINC-JP 11 67017917 67017917 single base substitution C T downstream_gene_variant LINC-JP 11 67017917 67017917 single base substitution C T exon_variant LINC-JP 11 67017917 67017917 single base substitution C T intron_variant LINC-JP 11 67017917 67017917 single base substitution C T missense_variant P264S 790C>T LINC-JP 11 67017917 67017917 single base substitution C T missense_variant P367S 1099C>T LINC-JP 11 67017917 67017917 single base substitution C T missense_variant P806S 2416C>T LINC-JP 11 67017917 67017917 single base substitution C T upstream_gene_variant LINC-JP 11 67021913 67021913 single base substitution A G intron_variant LINC-JP 11 67021969 67021969 single base substitution G C intron_variant LINC-JP 11 67028265 67028265 deletion of <=200bp A - downstream_gene_variant LIRI-JP 11 66883870 66883870 single base substitution G T upstream_gene_variant LIRI-JP 11 66887921 66887921 single base substitution A G intron_variant LIRI-JP 11 66888061 66888061 single base substitution A G intron_variant LIRI-JP 11 66888206 66888206 single base substitution A G intron_variant LIRI-JP 11 66889575 66889575 single base substitution A G intron_variant LIRI-JP 11 66894471 66894471 single base substitution C A intron_variant LIRI-JP 11 66895174 66895174 single base substitution A T intron_variant LIRI-JP 11 66895178 66895178 single base substitution T A intron_variant LIRI-JP 11 66895696 66895696 single base substitution A T intron_variant LIRI-JP 11 66899042 66899042 single base substitution C T intron_variant LIRI-JP 11 66899124 66899124 single base substitution C T intron_variant LIRI-JP 11 66899732 66899732 single base substitution A G intron_variant LIRI-JP 11 66900349 66900349 single base substitution A G intron_variant LIRI-JP 11 66901443 66901443 single base substitution G A intron_variant LIRI-JP 11 66903123 66903123 single base substitution C A intron_variant LIRI-JP 11 66905797 66905797 single base substitution G A intron_variant LIRI-JP 11 66907941 66907941 single base substitution G A intron_variant LIRI-JP 11 66908827 66908827 single base substitution T A intron_variant LIRI-JP 11 66913053 66913053 single base substitution G A intron_variant LIRI-JP 11 66913684 66913684 single base substitution T G intron_variant LIRI-JP 11 66918975 66918975 single base substitution A T downstream_gene_variant LIRI-JP 11 66918975 66918975 single base substitution A T intron_variant LIRI-JP 11 66919398 66919398 single base substitution G A downstream_gene_variant LIRI-JP 11 66919398 66919398 single base substitution G A intron_variant LIRI-JP 11 66920944 66920944 single base substitution T A downstream_gene_variant LIRI-JP 11 66920944 66920944 single base substitution T A intron_variant LIRI-JP 11 66924666 66924666 single base substitution C G intron_variant LIRI-JP 11 66924734 66924734 single base substitution A C intron_variant LIRI-JP 11 66924736 66924736 single base substitution A C intron_variant LIRI-JP 11 66924739 66924739 single base substitution G T intron_variant LIRI-JP 11 66925086 66925086 single base substitution C T intron_variant LIRI-JP 11 66927536 66927536 single base substitution C G intron_variant LIRI-JP 11 66929177 66929177 single base substitution G A intron_variant LIRI-JP 11 66929799 66929799 single base substitution A G intron_variant LIRI-JP 11 66930748 66930748 insertion of <=200bp - AGATGGCC intron_variant LIRI-JP 11 66932158 66932158 single base substitution C T intron_variant LIRI-JP 11 66932443 66932443 single base substitution A C intron_variant LIRI-JP 11 66932653 66932653 single base substitution C T intron_variant LIRI-JP 11 66933028 66933028 single base substitution A G intron_variant LIRI-JP 11 66933299 66933299 single base substitution T G intron_variant LIRI-JP 11 66934804 66934804 single base substitution A C intron_variant LIRI-JP 11 66936747 66936747 single base substitution C G intron_variant LIRI-JP 11 66937074 66937074 single base substitution T C intron_variant LIRI-JP 11 66939877 66939877 single base substitution A G intron_variant LIRI-JP 11 66942092 66942096 deletion of <=200bp TAATC - intron_variant LIRI-JP 11 66943831 66943831 single base substitution A G intron_variant LIRI-JP 11 66943993 66943993 single base substitution A C intron_variant LIRI-JP 11 66944857 66944857 single base substitution A G intron_variant LIRI-JP 11 66944918 66944918 single base substitution C G intron_variant LIRI-JP 11 66946835 66946835 single base substitution C A intron_variant LIRI-JP 11 66947485 66947485 single base substitution A G intron_variant LIRI-JP 11 66948318 66948318 single base substitution A G downstream_gene_variant LIRI-JP 11 66948318 66948318 single base substitution A G intron_variant LIRI-JP 11 66949052 66949052 single base substitution A G downstream_gene_variant LIRI-JP 11 66949052 66949052 single base substitution A G intron_variant LIRI-JP 11 66949427 66949427 single base substitution A G downstream_gene_variant LIRI-JP 11 66949427 66949427 single base substitution A G intron_variant LIRI-JP 11 66949514 66949514 single base substitution A G downstream_gene_variant LIRI-JP 11 66949514 66949514 single base substitution A G intron_variant LIRI-JP 11 66949600 66949600 single base substitution C G downstream_gene_variant LIRI-JP 11 66949600 66949600 single base substitution C G intron_variant LIRI-JP 11 66951299 66951299 single base substitution G T downstream_gene_variant LIRI-JP 11 66951299 66951299 single base substitution G T intron_variant LIRI-JP 11 66952993 66952993 single base substitution G A intron_variant LIRI-JP 11 66953683 66953683 single base substitution C A intron_variant LIRI-JP 11 66954942 66954942 single base substitution G T intron_variant LIRI-JP 11 66955325 66955325 single base substitution C T intron_variant LIRI-JP 11 66955344 66955344 single base substitution C G intron_variant LIRI-JP 11 66956408 66956408 single base substitution G A intron_variant LIRI-JP 11 66957024 66957024 single base substitution A T intron_variant LIRI-JP 11 66958087 66958087 single base substitution C G intron_variant LIRI-JP 11 66959940 66959940 single base substitution A G intron_variant LIRI-JP 11 66961080 66961080 single base substitution C A intron_variant LIRI-JP 11 66961685 66961685 single base substitution A G intron_variant LIRI-JP 11 66963650 66963650 single base substitution A G intron_variant LIRI-JP 11 66964948 66964948 single base substitution C T intron_variant LIRI-JP 11 66965240 66965240 single base substitution A G intron_variant LIRI-JP 11 66967085 66967085 single base substitution T A intron_variant LIRI-JP 11 66971571 66971571 single base substitution C T intron_variant LIRI-JP 11 66971571 66971571 single base substitution C T upstream_gene_variant LIRI-JP 11 66973010 66973010 single base substitution C G intron_variant LIRI-JP 11 66973010 66973010 single base substitution C G upstream_gene_variant LIRI-JP 11 66974340 66974340 single base substitution A G intron_variant LIRI-JP 11 66974340 66974340 single base substitution A G upstream_gene_variant LIRI-JP 11 66974426 66974426 single base substitution G T intron_variant LIRI-JP 11 66974426 66974426 single base substitution G T upstream_gene_variant LIRI-JP 11 66976620 66976620 single base substitution T C intron_variant LIRI-JP 11 66978185 66978185 single base substitution A G intron_variant LIRI-JP 11 66978812 66978812 single base substitution C T intron_variant LIRI-JP 11 66978812 66978812 single base substitution C T upstream_gene_variant LIRI-JP 11 66980090 66980090 single base substitution A G intron_variant LIRI-JP 11 66980090 66980090 single base substitution A G upstream_gene_variant LIRI-JP 11 66980236 66980236 single base substitution T G intron_variant LIRI-JP 11 66980236 66980236 single base substitution T G upstream_gene_variant LIRI-JP 11 66980673 66980673 single base substitution C G intron_variant LIRI-JP 11 66980673 66980673 single base substitution C G upstream_gene_variant LIRI-JP 11 66980686 66980686 single base substitution A G intron_variant LIRI-JP 11 66980686 66980686 single base substitution A G upstream_gene_variant LIRI-JP 11 66983270 66983270 single base substitution G T downstream_gene_variant LIRI-JP 11 66983270 66983270 single base substitution G T intron_variant LIRI-JP 11 66983270 66983270 single base substitution G T upstream_gene_variant LIRI-JP 11 66983874 66983874 single base substitution T A downstream_gene_variant LIRI-JP 11 66983874 66983874 single base substitution T A intron_variant LIRI-JP 11 66983874 66983874 single base substitution T A upstream_gene_variant LIRI-JP 11 66988569 66988569 single base substitution T C downstream_gene_variant LIRI-JP 11 66988569 66988569 single base substitution T C intron_variant LIRI-JP 11 66989018 66989018 single base substitution A G downstream_gene_variant LIRI-JP 11 66989018 66989018 single base substitution A G intron_variant LIRI-JP 11 66989307 66989307 single base substitution G T downstream_gene_variant LIRI-JP 11 66989307 66989307 single base substitution G T intron_variant LIRI-JP 11 66991489 66991489 single base substitution A G downstream_gene_variant LIRI-JP 11 66991489 66991489 single base substitution A G intron_variant LIRI-JP 11 66992495 66992495 single base substitution A G intron_variant LIRI-JP 11 66993557 66993557 single base substitution A G intron_variant LIRI-JP 11 66999796 66999796 single base substitution T A intron_variant LIRI-JP 11 66999955 66999958 deletion of <=200bp TTTA - intron_variant LIRI-JP 11 67000237 67000237 single base substitution G T intron_variant LIRI-JP 11 67002371 67002371 single base substitution A G intron_variant LIRI-JP 11 67003494 67003494 single base substitution A T intron_variant LIRI-JP 11 67003494 67003494 single base substitution A T upstream_gene_variant LIRI-JP 11 67004064 67004064 single base substitution C T intron_variant LIRI-JP 11 67004064 67004064 single base substitution C T upstream_gene_variant LIRI-JP 11 67005890 67005890 single base substitution A C intron_variant LIRI-JP 11 67005890 67005890 single base substitution A C upstream_gene_variant LIRI-JP 11 67006010 67006010 single base substitution A G intron_variant LIRI-JP 11 67006010 67006010 single base substitution A G upstream_gene_variant LIRI-JP 11 67007719 67007719 single base substitution A G 5_prime_UTR_variant LIRI-JP 11 67007719 67007719 single base substitution A G intron_variant LIRI-JP 11 67007719 67007719 single base substitution A G missense_variant D14G 41A>G LIRI-JP 11 67007719 67007719 single base substitution A G upstream_gene_variant LIRI-JP 11 67008765 67008765 single base substitution A G intron_variant LIRI-JP 11 67008765 67008765 single base substitution A G upstream_gene_variant LIRI-JP 11 67008898 67008898 single base substitution T A intron_variant LIRI-JP 11 67008898 67008898 single base substitution T A upstream_gene_variant LIRI-JP 11 67009220 67009220 single base substitution T G intron_variant LIRI-JP 11 67009220 67009220 single base substitution T G upstream_gene_variant LIRI-JP 11 67010415 67010415 single base substitution T C intron_variant LIRI-JP 11 67010415 67010415 single base substitution T C upstream_gene_variant LIRI-JP 11 67011169 67011169 single base substitution C G exon_variant LIRI-JP 11 67011169 67011169 single base substitution C G intron_variant LIRI-JP 11 67011169 67011169 single base substitution C G upstream_gene_variant LIRI-JP 11 67011938 67011938 single base substitution A T downstream_gene_variant LIRI-JP 11 67011938 67011938 single base substitution A T intron_variant LIRI-JP 11 67011938 67011938 single base substitution A T upstream_gene_variant LIRI-JP 11 67012798 67012798 single base substitution C T downstream_gene_variant LIRI-JP 11 67012798 67012798 single base substitution C T exon_variant LIRI-JP 11 67012798 67012798 single base substitution C T stop_gained R129* 385C>T LIRI-JP 11 67012798 67012798 single base substitution C T stop_gained R26* 76C>T LIRI-JP 11 67012798 67012798 single base substitution C T stop_gained R568* 1702C>T LIRI-JP 11 67012798 67012798 single base substitution C T upstream_gene_variant LIRI-JP 11 67013373 67013373 single base substitution A G downstream_gene_variant LIRI-JP 11 67013373 67013373 single base substitution A G exon_variant LIRI-JP 11 67013373 67013373 single base substitution A G intron_variant LIRI-JP 11 67013750 67013750 single base substitution A G downstream_gene_variant LIRI-JP 11 67013750 67013750 single base substitution A G intron_variant LIRI-JP 11 67015391 67015391 single base substitution A G downstream_gene_variant LIRI-JP 11 67015391 67015391 single base substitution A G intron_variant LIRI-JP 11 67015391 67015391 single base substitution A G upstream_gene_variant LIRI-JP 11 67017457 67017458 deletion of <=200bp TC - downstream_gene_variant LIRI-JP 11 67017457 67017458 deletion of <=200bp TC - intron_variant LIRI-JP 11 67017457 67017458 deletion of <=200bp TC - upstream_gene_variant LIRI-JP 11 67018071 67018071 single base substitution A T downstream_gene_variant LIRI-JP 11 67018071 67018071 single base substitution A T exon_variant LIRI-JP 11 67018071 67018071 single base substitution A T intron_variant LIRI-JP 11 67018071 67018071 single base substitution A T missense_variant E315V 944A>T LIRI-JP 11 67018071 67018071 single base substitution A T missense_variant E418V 1253A>T LIRI-JP 11 67018071 67018071 single base substitution A T missense_variant E857V 2570A>T LIRI-JP 11 67018071 67018071 single base substitution A T upstream_gene_variant LIRI-JP 11 67020567 67020567 single base substitution T G downstream_gene_variant LIRI-JP 11 67020567 67020567 single base substitution T G intron_variant LIRI-JP 11 67021450 67021450 single base substitution G T intron_variant LIRI-JP 11 67026069 67026069 single base substitution G A downstream_gene_variant LUSC-KR 11 66884437 66884437 single base substitution C T upstream_gene_variant LUSC-KR 11 66887099 66887099 single base substitution G C 5_prime_UTR_variant LUSC-KR 11 66887099 66887099 single base substitution G C upstream_gene_variant LUSC-KR 11 66887337 66887337 single base substitution A C 5_prime_UTR_variant LUSC-KR 11 66887337 66887337 single base substitution A C upstream_gene_variant LUSC-KR 11 66894514 66894514 single base substitution A C intron_variant LUSC-KR 11 66895174 66895174 single base substitution A T intron_variant LUSC-KR 11 66900396 66900396 single base substitution A G intron_variant LUSC-KR 11 66902321 66902321 single base substitution C T intron_variant LUSC-KR 11 66914721 66914721 single base substitution G C intron_variant LUSC-KR 11 66916883 66916883 single base substitution C G downstream_gene_variant LUSC-KR 11 66916883 66916883 single base substitution C G intron_variant LUSC-KR 11 66917211 66917211 single base substitution G T downstream_gene_variant LUSC-KR 11 66917211 66917211 single base substitution G T intron_variant LUSC-KR 11 66925361 66925361 single base substitution G T intron_variant LUSC-KR 11 66925470 66925470 single base substitution G A intron_variant LUSC-KR 11 66929212 66929212 single base substitution A G intron_variant LUSC-KR 11 66932580 66932580 single base substitution A G intron_variant LUSC-KR 11 66938203 66938203 single base substitution A G intron_variant LUSC-KR 11 66941233 66941233 single base substitution G T intron_variant LUSC-KR 11 66951050 66951050 single base substitution A T downstream_gene_variant LUSC-KR 11 66951050 66951050 single base substitution A T intron_variant LUSC-KR 11 66953599 66953599 single base substitution G C intron_variant LUSC-KR 11 66955771 66955771 single base substitution G T intron_variant LUSC-KR 11 66961888 66961888 single base substitution A T intron_variant LUSC-KR 11 66962865 66962865 single base substitution A G intron_variant LUSC-KR 11 66966137 66966137 single base substitution C T intron_variant LUSC-KR 11 66967582 66967582 single base substitution C T intron_variant LUSC-KR 11 66968296 66968296 single base substitution C T intron_variant LUSC-KR 11 66968726 66968726 single base substitution G T intron_variant LUSC-KR 11 66971107 66971107 single base substitution C G intron_variant LUSC-KR 11 66971107 66971107 single base substitution C G upstream_gene_variant LUSC-KR 11 66971981 66971981 single base substitution G T intron_variant LUSC-KR 11 66971981 66971981 single base substitution G T upstream_gene_variant LUSC-KR 11 66977397 66977397 single base substitution G T intron_variant LUSC-KR 11 66985865 66985865 single base substitution G C downstream_gene_variant LUSC-KR 11 66985865 66985865 single base substitution G C intron_variant LUSC-KR 11 66989150 66989150 single base substitution A G downstream_gene_variant LUSC-KR 11 66989150 66989150 single base substitution A G intron_variant LUSC-KR 11 66989551 66989551 single base substitution A T downstream_gene_variant LUSC-KR 11 66989551 66989551 single base substitution A T intron_variant LUSC-KR 11 66991429 66991429 single base substitution A T downstream_gene_variant LUSC-KR 11 66991429 66991429 single base substitution A T intron_variant LUSC-KR 11 66995723 66995723 single base substitution T C intron_variant LUSC-KR 11 66995723 66995723 single base substitution T C upstream_gene_variant LUSC-KR 11 66999348 66999348 single base substitution G A exon_variant LUSC-KR 11 66999348 66999348 single base substitution G A missense_variant D466N 1396G>A LUSC-KR 11 67003020 67003020 single base substitution C A intron_variant LUSC-KR 11 67003020 67003020 single base substitution C A upstream_gene_variant LUSC-KR 11 67009774 67009774 single base substitution T A intron_variant LUSC-KR 11 67009774 67009774 single base substitution T A upstream_gene_variant LUSC-KR 11 67014408 67014408 single base substitution T C downstream_gene_variant LUSC-KR 11 67014408 67014408 single base substitution T C intron_variant LUSC-KR 11 67025034 67025034 single base substitution A G 3_prime_UTR_variant LUSC-KR 11 67025034 67025034 single base substitution A G downstream_gene_variant LUSC-KR 11 67025034 67025034 single base substitution A G exon_variant LUSC-KR 11 67029743 67029743 single base substitution A T downstream_gene_variant LUSC-KR 11 67030552 67030552 single base substitution T A downstream_gene_variant LUSC-US 11 66947553 66947553 single base substitution G T exon_variant LUSC-US 11 66947553 66947553 single base substitution G T missense_variant G16C 46G>T LUSC-US 11 66983395 66983395 single base substitution G T downstream_gene_variant LUSC-US 11 66983395 66983395 single base substitution G T exon_variant LUSC-US 11 66983395 66983395 single base substitution G T missense_variant W221L 662G>T LUSC-US 11 66983395 66983395 single base substitution G T upstream_gene_variant LUSC-US 11 66995566 66995566 single base substitution G A exon_variant LUSC-US 11 66995566 66995566 single base substitution G A missense_variant R339H 1016G>A LUSC-US 11 66995566 66995566 single base substitution G A upstream_gene_variant LUSC-US 11 67017759 67017759 single base substitution G A downstream_gene_variant LUSC-US 11 67017759 67017759 single base substitution G A exon_variant LUSC-US 11 67017759 67017759 single base substitution G A missense_variant R211H 632G>A LUSC-US 11 67017759 67017759 single base substitution G A missense_variant R314H 941G>A LUSC-US 11 67017759 67017759 single base substitution G A missense_variant R753H 2258G>A LUSC-US 11 67017759 67017759 single base substitution G A upstream_gene_variant MALY-DE 11 66883829 66883829 deletion of <=200bp G - upstream_gene_variant MALY-DE 11 66884959 66884959 single base substitution C T upstream_gene_variant MALY-DE 11 66893886 66893886 single base substitution G T intron_variant MALY-DE 11 66903960 66903960 single base substitution A T intron_variant MALY-DE 11 66910399 66910399 single base substitution T C intron_variant MALY-DE 11 66914613 66914629 deletion of <=200bp TGTTGTTGACAGTTTGG - intron_variant MALY-DE 11 66922223 66922223 single base substitution T C intron_variant MALY-DE 11 66923464 66923464 single base substitution A T intron_variant MALY-DE 11 66925733 66925733 single base substitution C G intron_variant MALY-DE 11 66931984 66931984 single base substitution T G intron_variant MALY-DE 11 66936231 66936231 single base substitution A G intron_variant MALY-DE 11 66936274 66936274 single base substitution T C intron_variant MALY-DE 11 66941838 66941838 single base substitution A T intron_variant MALY-DE 11 66948975 66948975 single base substitution T C downstream_gene_variant MALY-DE 11 66948975 66948975 single base substitution T C intron_variant MALY-DE 11 66958056 66958056 single base substitution C A intron_variant MALY-DE 11 66958527 66958527 insertion of <=200bp - T intron_variant MALY-DE 11 66960175 66960175 single base substitution C G intron_variant MALY-DE 11 66972602 66972602 single base substitution A G intron_variant MALY-DE 11 66972602 66972602 single base substitution A G upstream_gene_variant MALY-DE 11 66975678 66975678 single base substitution A T intron_variant MALY-DE 11 66982341 66982341 single base substitution A G intron_variant MALY-DE 11 66982341 66982341 single base substitution A G upstream_gene_variant MALY-DE 11 66983515 66983515 single base substitution T G downstream_gene_variant MALY-DE 11 66983515 66983515 single base substitution T G intron_variant MALY-DE 11 66983515 66983515 single base substitution T G upstream_gene_variant MALY-DE 11 66983524 66983524 single base substitution A T downstream_gene_variant MALY-DE 11 66983524 66983524 single base substitution A T intron_variant MALY-DE 11 66983524 66983524 single base substitution A T upstream_gene_variant MALY-DE 11 66983560 66983560 single base substitution A C downstream_gene_variant MALY-DE 11 66983560 66983560 single base substitution A C intron_variant MALY-DE 11 66983560 66983560 single base substitution A C upstream_gene_variant MALY-DE 11 66985933 66985933 single base substitution C A downstream_gene_variant MALY-DE 11 66985933 66985933 single base substitution C A intron_variant MALY-DE 11 66985982 66985982 single base substitution T C downstream_gene_variant MALY-DE 11 66985982 66985982 single base substitution T C intron_variant MALY-DE 11 67003062 67003062 single base substitution G A intron_variant MALY-DE 11 67003062 67003062 single base substitution G A upstream_gene_variant MALY-DE 11 67012215 67012215 single base substitution G A downstream_gene_variant MALY-DE 11 67012215 67012215 single base substitution G A intron_variant MALY-DE 11 67012215 67012215 single base substitution G A upstream_gene_variant MALY-DE 11 67016084 67016084 single base substitution T G downstream_gene_variant MALY-DE 11 67016084 67016084 single base substitution T G intron_variant MALY-DE 11 67016084 67016084 single base substitution T G upstream_gene_variant MALY-DE 11 67016086 67016086 single base substitution T A downstream_gene_variant MALY-DE 11 67016086 67016086 single base substitution T A intron_variant MALY-DE 11 67016086 67016086 single base substitution T A upstream_gene_variant MALY-DE 11 67019325 67019325 single base substitution A C downstream_gene_variant MALY-DE 11 67019325 67019325 single base substitution A C intron_variant MALY-DE 11 67019325 67019325 single base substitution A C upstream_gene_variant MALY-DE 11 67022116 67022116 single base substitution G A intron_variant MELA-AU 11 66881741 66881741 single base substitution G A upstream_gene_variant MELA-AU 11 66881920 66881920 single base substitution G A upstream_gene_variant MELA-AU 11 66881971 66881971 single base substitution G A upstream_gene_variant MELA-AU 11 66883700 66883700 single base substitution C T upstream_gene_variant MELA-AU 11 66883731 66883731 single base substitution C T upstream_gene_variant MELA-AU 11 66883736 66883736 single base substitution G T upstream_gene_variant MELA-AU 11 66884593 66884593 single base substitution C G upstream_gene_variant MELA-AU 11 66884662 66884662 single base substitution C T upstream_gene_variant MELA-AU 11 66885151 66885152 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 66890085 66890085 single base substitution C T intron_variant MELA-AU 11 66890658 66890658 single base substitution C T intron_variant MELA-AU 11 66891025 66891025 single base substitution C T intron_variant MELA-AU 11 66891029 66891029 single base substitution C T intron_variant MELA-AU 11 66891119 66891119 single base substitution G A intron_variant MELA-AU 11 66891393 66891393 single base substitution C T intron_variant MELA-AU 11 66891444 66891445 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 66891874 66891874 single base substitution C T intron_variant MELA-AU 11 66892595 66892596 multiple base substitution (>=2bp and <=200bp) GT AG intron_variant MELA-AU 11 66892997 66892997 single base substitution C G intron_variant MELA-AU 11 66893764 66893764 single base substitution T A intron_variant MELA-AU 11 66893909 66893909 single base substitution T C intron_variant MELA-AU 11 66893997 66893997 single base substitution G A intron_variant MELA-AU 11 66894603 66894603 single base substitution C T intron_variant MELA-AU 11 66895104 66895104 single base substitution C T intron_variant MELA-AU 11 66895438 66895438 single base substitution C T intron_variant MELA-AU 11 66895957 66895957 single base substitution C T intron_variant MELA-AU 11 66896613 66896613 single base substitution C T intron_variant MELA-AU 11 66896753 66896753 single base substitution C T intron_variant MELA-AU 11 66896807 66896807 single base substitution C T intron_variant MELA-AU 11 66896953 66896953 single base substitution C T intron_variant MELA-AU 11 66897107 66897107 single base substitution A T intron_variant MELA-AU 11 66897461 66897461 single base substitution T G intron_variant MELA-AU 11 66897524 66897524 single base substitution C T intron_variant MELA-AU 11 66897937 66897937 single base substitution C T intron_variant MELA-AU 11 66898850 66898850 single base substitution C T intron_variant MELA-AU 11 66899292 66899292 single base substitution C T intron_variant MELA-AU 11 66899538 66899538 single base substitution C T intron_variant MELA-AU 11 66900653 66900653 single base substitution C T intron_variant MELA-AU 11 66900680 66900680 single base substitution C T intron_variant MELA-AU 11 66901133 66901133 single base substitution C T intron_variant MELA-AU 11 66901833 66901833 single base substitution C G intron_variant MELA-AU 11 66902217 66902217 single base substitution C T intron_variant MELA-AU 11 66902867 66902867 single base substitution A T intron_variant MELA-AU 11 66904212 66904212 single base substitution C T intron_variant MELA-AU 11 66904313 66904313 single base substitution C T intron_variant MELA-AU 11 66904743 66904744 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 66906298 66906298 single base substitution C T intron_variant MELA-AU 11 66906727 66906727 single base substitution T G intron_variant MELA-AU 11 66907134 66907134 single base substitution G T intron_variant MELA-AU 11 66907244 66907244 single base substitution G A intron_variant MELA-AU 11 66907377 66907377 single base substitution C T intron_variant MELA-AU 11 66909236 66909236 single base substitution C T intron_variant MELA-AU 11 66909632 66909632 single base substitution C T intron_variant MELA-AU 11 66910765 66910766 multiple base substitution (>=2bp and <=200bp) AC CT exon_variant MELA-AU 11 66910765 66910766 multiple base substitution (>=2bp and <=200bp) AC CT intron_variant MELA-AU 11 66911145 66911145 single base substitution C T intron_variant MELA-AU 11 66911503 66911504 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 66911568 66911568 single base substitution C A intron_variant MELA-AU 11 66911577 66911577 single base substitution C T intron_variant MELA-AU 11 66914188 66914189 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 66914609 66914609 single base substitution A G intron_variant MELA-AU 11 66914773 66914773 single base substitution G A intron_variant MELA-AU 11 66915272 66915272 single base substitution C T intron_variant MELA-AU 11 66915383 66915383 single base substitution C T intron_variant MELA-AU 11 66916137 66916137 single base substitution T G intron_variant MELA-AU 11 66916155 66916155 single base substitution C T intron_variant MELA-AU 11 66916266 66916266 single base substitution C T intron_variant MELA-AU 11 66916883 66916883 single base substitution C T downstream_gene_variant MELA-AU 11 66916883 66916883 single base substitution C T intron_variant MELA-AU 11 66917509 66917509 single base substitution G A downstream_gene_variant MELA-AU 11 66917509 66917509 single base substitution G A intron_variant MELA-AU 11 66918065 66918065 single base substitution C T downstream_gene_variant MELA-AU 11 66918065 66918065 single base substitution C T intron_variant MELA-AU 11 66918476 66918476 single base substitution A T downstream_gene_variant MELA-AU 11 66918476 66918476 single base substitution A T intron_variant MELA-AU 11 66919551 66919551 single base substitution C T downstream_gene_variant MELA-AU 11 66919551 66919551 single base substitution C T intron_variant MELA-AU 11 66920875 66920875 single base substitution C T downstream_gene_variant MELA-AU 11 66920875 66920875 single base substitution C T intron_variant MELA-AU 11 66921034 66921035 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 66921034 66921035 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 66921112 66921112 single base substitution A G downstream_gene_variant MELA-AU 11 66921112 66921112 single base substitution A G intron_variant MELA-AU 11 66921344 66921344 single base substitution C T downstream_gene_variant MELA-AU 11 66921344 66921344 single base substitution C T intron_variant MELA-AU 11 66921380 66921380 single base substitution C T downstream_gene_variant MELA-AU 11 66921380 66921380 single base substitution C T intron_variant MELA-AU 11 66921568 66921568 single base substitution A C downstream_gene_variant MELA-AU 11 66921568 66921568 single base substitution A C intron_variant MELA-AU 11 66922076 66922076 single base substitution C T intron_variant MELA-AU 11 66923038 66923038 single base substitution T C intron_variant MELA-AU 11 66923146 66923147 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 66923159 66923159 single base substitution C T intron_variant MELA-AU 11 66923998 66923998 single base substitution C T intron_variant MELA-AU 11 66924678 66924678 single base substitution G A intron_variant MELA-AU 11 66924696 66924696 single base substitution A G intron_variant MELA-AU 11 66924753 66924753 single base substitution C T intron_variant MELA-AU 11 66925676 66925676 single base substitution G A intron_variant MELA-AU 11 66927568 66927568 single base substitution C T intron_variant MELA-AU 11 66927855 66927855 single base substitution A T intron_variant MELA-AU 11 66928071 66928071 single base substitution C T intron_variant MELA-AU 11 66929906 66929906 single base substitution C T intron_variant MELA-AU 11 66930205 66930205 single base substitution G A intron_variant MELA-AU 11 66930892 66930892 single base substitution A T intron_variant MELA-AU 11 66931241 66931241 single base substitution C T intron_variant MELA-AU 11 66931540 66931540 single base substitution G A intron_variant MELA-AU 11 66932328 66932328 single base substitution C T intron_variant MELA-AU 11 66933042 66933042 single base substitution C A intron_variant MELA-AU 11 66933945 66933945 single base substitution C G intron_variant MELA-AU 11 66934029 66934029 single base substitution T A intron_variant MELA-AU 11 66934048 66934048 single base substitution T C intron_variant MELA-AU 11 66934938 66934938 single base substitution C T intron_variant MELA-AU 11 66935513 66935513 single base substitution C G intron_variant MELA-AU 11 66936415 66936415 single base substitution C T intron_variant MELA-AU 11 66937206 66937206 single base substitution C T intron_variant MELA-AU 11 66937462 66937462 single base substitution C T intron_variant MELA-AU 11 66938285 66938285 single base substitution C T intron_variant MELA-AU 11 66938510 66938510 single base substitution G A intron_variant MELA-AU 11 66938513 66938513 single base substitution T A intron_variant MELA-AU 11 66938643 66938643 single base substitution A G intron_variant MELA-AU 11 66938766 66938766 single base substitution C T intron_variant MELA-AU 11 66939063 66939063 single base substitution G C intron_variant MELA-AU 11 66939468 66939468 single base substitution C T intron_variant MELA-AU 11 66939918 66939918 single base substitution C T intron_variant MELA-AU 11 66940433 66940433 single base substitution T A intron_variant MELA-AU 11 66940824 66940824 single base substitution C T intron_variant MELA-AU 11 66941289 66941289 single base substitution T A intron_variant MELA-AU 11 66941909 66941909 single base substitution C T intron_variant MELA-AU 11 66942105 66942105 single base substitution C T intron_variant MELA-AU 11 66942808 66942808 single base substitution G A intron_variant MELA-AU 11 66945729 66945729 single base substitution C T intron_variant MELA-AU 11 66946503 66946503 single base substitution C T intron_variant MELA-AU 11 66946586 66946586 single base substitution A G intron_variant MELA-AU 11 66947999 66947999 single base substitution C T downstream_gene_variant MELA-AU 11 66947999 66947999 single base substitution C T intron_variant MELA-AU 11 66948721 66948721 single base substitution T A downstream_gene_variant MELA-AU 11 66948721 66948721 single base substitution T A intron_variant MELA-AU 11 66949209 66949209 single base substitution T C downstream_gene_variant MELA-AU 11 66949209 66949209 single base substitution T C intron_variant MELA-AU 11 66949706 66949706 single base substitution C T downstream_gene_variant MELA-AU 11 66949706 66949706 single base substitution C T intron_variant MELA-AU 11 66950575 66950575 single base substitution C T downstream_gene_variant MELA-AU 11 66950575 66950575 single base substitution C T intron_variant MELA-AU 11 66950929 66950929 single base substitution C T downstream_gene_variant MELA-AU 11 66950929 66950929 single base substitution C T intron_variant MELA-AU 11 66950957 66950957 single base substitution C T downstream_gene_variant MELA-AU 11 66950957 66950957 single base substitution C T intron_variant MELA-AU 11 66951165 66951165 single base substitution C T downstream_gene_variant MELA-AU 11 66951165 66951165 single base substitution C T intron_variant MELA-AU 11 66951522 66951522 single base substitution T C downstream_gene_variant MELA-AU 11 66951522 66951522 single base substitution T C intron_variant MELA-AU 11 66951793 66951793 single base substitution C T downstream_gene_variant MELA-AU 11 66951793 66951793 single base substitution C T intron_variant MELA-AU 11 66952046 66952046 single base substitution G A downstream_gene_variant MELA-AU 11 66952046 66952046 single base substitution G A intron_variant MELA-AU 11 66952637 66952637 single base substitution C T downstream_gene_variant MELA-AU 11 66952637 66952637 single base substitution C T intron_variant MELA-AU 11 66952983 66952983 single base substitution C T intron_variant MELA-AU 11 66953016 66953016 single base substitution T C intron_variant MELA-AU 11 66953130 66953131 multiple base substitution (>=2bp and <=200bp) CC GT intron_variant MELA-AU 11 66953266 66953266 single base substitution C T intron_variant MELA-AU 11 66953860 66953860 single base substitution C T intron_variant MELA-AU 11 66954590 66954590 single base substitution C T intron_variant MELA-AU 11 66954939 66954939 single base substitution C T intron_variant MELA-AU 11 66955025 66955025 single base substitution T C intron_variant MELA-AU 11 66955031 66955031 single base substitution A G intron_variant MELA-AU 11 66955037 66955037 single base substitution T C intron_variant MELA-AU 11 66955466 66955467 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 66955758 66955759 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 66955964 66955964 single base substitution A G intron_variant MELA-AU 11 66956683 66956683 single base substitution C T intron_variant MELA-AU 11 66957562 66957562 single base substitution G A intron_variant MELA-AU 11 66957665 66957665 single base substitution G A intron_variant MELA-AU 11 66958800 66958800 single base substitution G A intron_variant MELA-AU 11 66958815 66958815 single base substitution C G intron_variant MELA-AU 11 66960346 66960346 single base substitution C T intron_variant MELA-AU 11 66960467 66960467 single base substitution T A intron_variant MELA-AU 11 66960706 66960707 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 66961129 66961129 single base substitution C T intron_variant MELA-AU 11 66961625 66961625 single base substitution C T intron_variant MELA-AU 11 66962126 66962126 single base substitution C T intron_variant MELA-AU 11 66962451 66962451 single base substitution G A intron_variant MELA-AU 11 66963393 66963393 single base substitution C T intron_variant MELA-AU 11 66963458 66963458 insertion of <=200bp - T intron_variant MELA-AU 11 66963638 66963638 single base substitution C T intron_variant MELA-AU 11 66963836 66963836 single base substitution C T intron_variant MELA-AU 11 66964139 66964139 single base substitution G A intron_variant MELA-AU 11 66964275 66964275 single base substitution C G intron_variant MELA-AU 11 66964358 66964358 single base substitution C T intron_variant MELA-AU 11 66965052 66965052 single base substitution C T intron_variant MELA-AU 11 66965206 66965206 single base substitution A G intron_variant MELA-AU 11 66967133 66967133 single base substitution T C intron_variant MELA-AU 11 66967847 66967847 single base substitution C T intron_variant MELA-AU 11 66968491 66968491 single base substitution G A intron_variant MELA-AU 11 66968614 66968614 single base substitution G A intron_variant MELA-AU 11 66968687 66968687 single base substitution A G intron_variant MELA-AU 11 66968690 66968690 insertion of <=200bp - TGTGTG intron_variant MELA-AU 11 66968706 66968706 insertion of <=200bp - TGTGTGTA intron_variant MELA-AU 11 66968861 66968861 single base substitution C T intron_variant MELA-AU 11 66969281 66969281 single base substitution C T intron_variant MELA-AU 11 66969349 66969349 single base substitution C T intron_variant MELA-AU 11 66969523 66969523 single base substitution C T intron_variant MELA-AU 11 66970434 66970434 single base substitution C T intron_variant MELA-AU 11 66970434 66970434 single base substitution C T upstream_gene_variant MELA-AU 11 66970779 66970779 single base substitution A G intron_variant MELA-AU 11 66970779 66970779 single base substitution A G upstream_gene_variant MELA-AU 11 66970924 66970924 single base substitution A C intron_variant MELA-AU 11 66970924 66970924 single base substitution A C upstream_gene_variant MELA-AU 11 66970934 66970935 multiple base substitution (>=2bp and <=200bp) AT TC intron_variant MELA-AU 11 66970934 66970935 multiple base substitution (>=2bp and <=200bp) AT TC upstream_gene_variant MELA-AU 11 66971379 66971379 single base substitution C T intron_variant MELA-AU 11 66971379 66971379 single base substitution C T upstream_gene_variant MELA-AU 11 66972935 66972935 single base substitution C T intron_variant MELA-AU 11 66972935 66972935 single base substitution C T upstream_gene_variant MELA-AU 11 66973211 66973211 single base substitution C T intron_variant MELA-AU 11 66973211 66973211 single base substitution C T upstream_gene_variant MELA-AU 11 66973884 66973884 single base substitution A T intron_variant MELA-AU 11 66973884 66973884 single base substitution A T upstream_gene_variant MELA-AU 11 66974635 66974635 single base substitution T C intron_variant MELA-AU 11 66974635 66974635 single base substitution T C upstream_gene_variant MELA-AU 11 66974859 66974859 single base substitution C T intron_variant MELA-AU 11 66974859 66974859 single base substitution C T upstream_gene_variant MELA-AU 11 66975093 66975093 single base substitution C T exon_variant MELA-AU 11 66975093 66975093 single base substitution C T synonymous_variant L140L 420C>T MELA-AU 11 66976655 66976655 single base substitution C T intron_variant MELA-AU 11 66976816 66976816 single base substitution G A intron_variant MELA-AU 11 66978040 66978040 single base substitution T A intron_variant MELA-AU 11 66978281 66978281 single base substitution T C intron_variant MELA-AU 11 66979009 66979009 single base substitution C T intron_variant MELA-AU 11 66979009 66979009 single base substitution C T upstream_gene_variant MELA-AU 11 66979157 66979157 single base substitution A G intron_variant MELA-AU 11 66979157 66979157 single base substitution A G upstream_gene_variant MELA-AU 11 66980004 66980004 single base substitution C T intron_variant MELA-AU 11 66980004 66980004 single base substitution C T upstream_gene_variant MELA-AU 11 66980681 66980681 single base substitution A T intron_variant MELA-AU 11 66980681 66980681 single base substitution A T upstream_gene_variant MELA-AU 11 66981839 66981839 single base substitution C T intron_variant MELA-AU 11 66981839 66981839 single base substitution C T upstream_gene_variant MELA-AU 11 66982105 66982105 single base substitution C T intron_variant MELA-AU 11 66982105 66982105 single base substitution C T upstream_gene_variant MELA-AU 11 66982213 66982213 single base substitution G A intron_variant MELA-AU 11 66982213 66982213 single base substitution G A upstream_gene_variant MELA-AU 11 66982481 66982481 single base substitution T A intron_variant MELA-AU 11 66982481 66982481 single base substitution T A upstream_gene_variant MELA-AU 11 66982944 66982944 single base substitution C T exon_variant MELA-AU 11 66982944 66982944 single base substitution C T intron_variant MELA-AU 11 66982944 66982944 single base substitution C T upstream_gene_variant MELA-AU 11 66983536 66983536 single base substitution C T downstream_gene_variant MELA-AU 11 66983536 66983536 single base substitution C T intron_variant MELA-AU 11 66983536 66983536 single base substitution C T upstream_gene_variant MELA-AU 11 66986026 66986026 single base substitution T A downstream_gene_variant MELA-AU 11 66986026 66986026 single base substitution T A intron_variant MELA-AU 11 66987248 66987248 single base substitution C T downstream_gene_variant MELA-AU 11 66987248 66987248 single base substitution C T intron_variant MELA-AU 11 66987279 66987279 single base substitution C T downstream_gene_variant MELA-AU 11 66987279 66987279 single base substitution C T intron_variant MELA-AU 11 66987366 66987366 single base substitution C T downstream_gene_variant MELA-AU 11 66987366 66987366 single base substitution C T intron_variant MELA-AU 11 66987818 66987818 single base substitution C T downstream_gene_variant MELA-AU 11 66987818 66987818 single base substitution C T intron_variant MELA-AU 11 66988013 66988013 single base substitution A G downstream_gene_variant MELA-AU 11 66988013 66988013 single base substitution A G intron_variant MELA-AU 11 66988700 66988700 single base substitution G A downstream_gene_variant MELA-AU 11 66988700 66988700 single base substitution G A intron_variant MELA-AU 11 66989012 66989012 single base substitution T C downstream_gene_variant MELA-AU 11 66989012 66989012 single base substitution T C intron_variant MELA-AU 11 66990273 66990273 single base substitution C T downstream_gene_variant MELA-AU 11 66990273 66990273 single base substitution C T intron_variant MELA-AU 11 66990326 66990326 single base substitution C T downstream_gene_variant MELA-AU 11 66990326 66990326 single base substitution C T intron_variant MELA-AU 11 66990657 66990658 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 66990657 66990658 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 66991088 66991088 single base substitution C T downstream_gene_variant MELA-AU 11 66991088 66991088 single base substitution C T intron_variant MELA-AU 11 66991263 66991263 single base substitution C T downstream_gene_variant MELA-AU 11 66991263 66991263 single base substitution C T intron_variant MELA-AU 11 66991404 66991404 deletion of <=200bp A - downstream_gene_variant MELA-AU 11 66991404 66991404 deletion of <=200bp A - intron_variant MELA-AU 11 66991651 66991651 single base substitution C T downstream_gene_variant MELA-AU 11 66991651 66991651 single base substitution C T intron_variant MELA-AU 11 66992043 66992043 single base substitution A G downstream_gene_variant MELA-AU 11 66992043 66992043 single base substitution A G intron_variant MELA-AU 11 66992246 66992246 single base substitution C T intron_variant MELA-AU 11 66992656 66992656 single base substitution C T intron_variant MELA-AU 11 66993039 66993039 single base substitution C T intron_variant MELA-AU 11 66993578 66993578 single base substitution A G intron_variant MELA-AU 11 66994020 66994020 single base substitution C T intron_variant MELA-AU 11 66996396 66996396 single base substitution C T intron_variant MELA-AU 11 66996396 66996396 single base substitution C T upstream_gene_variant MELA-AU 11 66997309 66997309 single base substitution C T intron_variant MELA-AU 11 66997309 66997309 single base substitution C T upstream_gene_variant MELA-AU 11 66998292 66998292 single base substitution C T intron_variant MELA-AU 11 66998292 66998292 single base substitution C T upstream_gene_variant MELA-AU 11 66999195 66999195 single base substitution C T exon_variant MELA-AU 11 66999195 66999195 single base substitution C T missense_variant P415S 1243C>T MELA-AU 11 66999195 66999195 single base substitution C T upstream_gene_variant MELA-AU 11 66999244 66999244 single base substitution G A exon_variant MELA-AU 11 66999244 66999244 single base substitution G A missense_variant R431Q 1292G>A MELA-AU 11 66999275 66999275 single base substitution C T exon_variant MELA-AU 11 66999275 66999275 single base substitution C T synonymous_variant P441P 1323C>T MELA-AU 11 66999588 66999588 single base substitution C T intron_variant MELA-AU 11 66999612 66999612 single base substitution C T intron_variant MELA-AU 11 67000157 67000157 single base substitution T C intron_variant MELA-AU 11 67000520 67000520 single base substitution C T intron_variant MELA-AU 11 67000597 67000598 multiple base substitution (>=2bp and <=200bp) GG AC intron_variant MELA-AU 11 67000873 67000873 single base substitution C T intron_variant MELA-AU 11 67003607 67003607 single base substitution T C intron_variant MELA-AU 11 67003607 67003607 single base substitution T C upstream_gene_variant MELA-AU 11 67004026 67004026 single base substitution C T intron_variant MELA-AU 11 67004026 67004026 single base substitution C T upstream_gene_variant MELA-AU 11 67004956 67004956 single base substitution C T intron_variant MELA-AU 11 67004956 67004956 single base substitution C T upstream_gene_variant MELA-AU 11 67006571 67006571 single base substitution G A intron_variant MELA-AU 11 67006571 67006571 single base substitution G A upstream_gene_variant MELA-AU 11 67006633 67006633 single base substitution T A intron_variant MELA-AU 11 67006633 67006633 single base substitution T A upstream_gene_variant MELA-AU 11 67006728 67006728 single base substitution G A intron_variant MELA-AU 11 67006728 67006728 single base substitution G A upstream_gene_variant MELA-AU 11 67008212 67008212 single base substitution G A intron_variant MELA-AU 11 67008212 67008212 single base substitution G A upstream_gene_variant MELA-AU 11 67008214 67008214 single base substitution T G intron_variant MELA-AU 11 67008214 67008214 single base substitution T G upstream_gene_variant MELA-AU 11 67009143 67009143 single base substitution C T intron_variant MELA-AU 11 67009143 67009143 single base substitution C T upstream_gene_variant MELA-AU 11 67010797 67010797 single base substitution C T intron_variant MELA-AU 11 67010797 67010797 single base substitution C T upstream_gene_variant MELA-AU 11 67011734 67011734 single base substitution T A downstream_gene_variant MELA-AU 11 67011734 67011734 single base substitution T A intron_variant MELA-AU 11 67011734 67011734 single base substitution T A upstream_gene_variant MELA-AU 11 67013187 67013187 single base substitution C T downstream_gene_variant MELA-AU 11 67013187 67013187 single base substitution C T exon_variant MELA-AU 11 67013187 67013187 single base substitution C T intron_variant MELA-AU 11 67014153 67014153 single base substitution C T downstream_gene_variant MELA-AU 11 67014153 67014153 single base substitution C T intron_variant MELA-AU 11 67014724 67014724 single base substitution C G downstream_gene_variant MELA-AU 11 67014724 67014724 single base substitution C G intron_variant MELA-AU 11 67014930 67014930 single base substitution C T downstream_gene_variant MELA-AU 11 67014930 67014930 single base substitution C T intron_variant MELA-AU 11 67014930 67014930 single base substitution C T upstream_gene_variant MELA-AU 11 67015140 67015140 single base substitution C T downstream_gene_variant MELA-AU 11 67015140 67015140 single base substitution C T intron_variant MELA-AU 11 67015140 67015140 single base substitution C T upstream_gene_variant MELA-AU 11 67015680 67015680 single base substitution C T downstream_gene_variant MELA-AU 11 67015680 67015680 single base substitution C T intron_variant MELA-AU 11 67015680 67015680 single base substitution C T upstream_gene_variant MELA-AU 11 67016015 67016015 single base substitution G A downstream_gene_variant MELA-AU 11 67016015 67016015 single base substitution G A intron_variant MELA-AU 11 67016015 67016015 single base substitution G A splice_acceptor_variant MELA-AU 11 67016015 67016015 single base substitution G A upstream_gene_variant MELA-AU 11 67017840 67017840 single base substitution C T downstream_gene_variant MELA-AU 11 67017840 67017840 single base substitution C T exon_variant MELA-AU 11 67017840 67017840 single base substitution C T intron_variant MELA-AU 11 67017840 67017840 single base substitution C T missense_variant P238L 713C>T MELA-AU 11 67017840 67017840 single base substitution C T missense_variant P341L 1022C>T MELA-AU 11 67017840 67017840 single base substitution C T missense_variant P780L 2339C>T MELA-AU 11 67017840 67017840 single base substitution C T upstream_gene_variant MELA-AU 11 67018169 67018169 single base substitution G A downstream_gene_variant MELA-AU 11 67018169 67018169 single base substitution G A exon_variant MELA-AU 11 67018169 67018169 single base substitution G A intron_variant MELA-AU 11 67018169 67018169 single base substitution G A missense_variant E348K 1042G>A MELA-AU 11 67018169 67018169 single base substitution G A missense_variant E451K 1351G>A MELA-AU 11 67018169 67018169 single base substitution G A missense_variant E890K 2668G>A MELA-AU 11 67018169 67018169 single base substitution G A upstream_gene_variant MELA-AU 11 67018602 67018602 single base substitution C T downstream_gene_variant MELA-AU 11 67018602 67018602 single base substitution C T intron_variant MELA-AU 11 67018602 67018602 single base substitution C T upstream_gene_variant MELA-AU 11 67020065 67020066 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 67020065 67020066 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 11 67020065 67020066 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 67020126 67020126 single base substitution C T downstream_gene_variant MELA-AU 11 67020126 67020126 single base substitution C T exon_variant MELA-AU 11 67020126 67020126 single base substitution C T intron_variant MELA-AU 11 67021141 67021141 single base substitution G A intron_variant MELA-AU 11 67021218 67021218 single base substitution T G intron_variant MELA-AU 11 67021952 67021952 single base substitution G A intron_variant MELA-AU 11 67022403 67022403 single base substitution C T 3_prime_UTR_variant MELA-AU 11 67022403 67022403 single base substitution C T exon_variant MELA-AU 11 67022403 67022403 single base substitution C T synonymous_variant T1122T 3366C>T MELA-AU 11 67022403 67022403 single base substitution C T synonymous_variant T580T 1740C>T MELA-AU 11 67022403 67022403 single base substitution C T synonymous_variant T683T 2049C>T MELA-AU 11 67022650 67022650 single base substitution C A 3_prime_UTR_variant MELA-AU 11 67022650 67022650 single base substitution C A exon_variant MELA-AU 11 67022920 67022920 single base substitution A T 3_prime_UTR_variant MELA-AU 11 67022920 67022920 single base substitution A T exon_variant MELA-AU 11 67024518 67024519 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 11 67024518 67024519 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 67024518 67024519 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 11 67024556 67024556 single base substitution G A 3_prime_UTR_variant MELA-AU 11 67024556 67024556 single base substitution G A downstream_gene_variant MELA-AU 11 67024556 67024556 single base substitution G A exon_variant MELA-AU 11 67024874 67024874 single base substitution C T 3_prime_UTR_variant MELA-AU 11 67024874 67024874 single base substitution C T downstream_gene_variant MELA-AU 11 67024874 67024874 single base substitution C T exon_variant MELA-AU 11 67025116 67025116 single base substitution T C 3_prime_UTR_variant MELA-AU 11 67025116 67025116 single base substitution T C downstream_gene_variant MELA-AU 11 67025116 67025116 single base substitution T C exon_variant MELA-AU 11 67025492 67025492 single base substitution T G 3_prime_UTR_variant MELA-AU 11 67025492 67025492 single base substitution T G downstream_gene_variant MELA-AU 11 67025783 67025783 single base substitution C T downstream_gene_variant MELA-AU 11 67026407 67026408 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 67027080 67027080 single base substitution C T downstream_gene_variant MELA-AU 11 67027278 67027278 single base substitution C T downstream_gene_variant MELA-AU 11 67027504 67027504 single base substitution C T downstream_gene_variant MELA-AU 11 67027623 67027623 single base substitution G A downstream_gene_variant MELA-AU 11 67029284 67029284 single base substitution G A downstream_gene_variant MELA-AU 11 67030007 67030007 single base substitution C T downstream_gene_variant MELA-AU 11 67030191 67030191 single base substitution G A downstream_gene_variant MELA-AU 11 67030460 67030460 single base substitution C T downstream_gene_variant ORCA-IN 11 66935308 66935308 single base substitution C T intron_variant ORCA-IN 11 66940089 66940089 single base substitution G T intron_variant ORCA-IN 11 66960583 66960583 single base substitution C G intron_variant ORCA-IN 11 66973006 66973006 single base substitution C G intron_variant ORCA-IN 11 66973006 66973006 single base substitution C G upstream_gene_variant ORCA-IN 11 66992017 66992017 single base substitution C A downstream_gene_variant ORCA-IN 11 66992017 66992017 single base substitution C A intron_variant ORCA-IN 11 67018132 67018132 single base substitution G T downstream_gene_variant ORCA-IN 11 67018132 67018132 single base substitution G T exon_variant ORCA-IN 11 67018132 67018132 single base substitution G T intron_variant ORCA-IN 11 67018132 67018132 single base substitution G T missense_variant R335S 1005G>T ORCA-IN 11 67018132 67018132 single base substitution G T missense_variant R438S 1314G>T ORCA-IN 11 67018132 67018132 single base substitution G T missense_variant R877S 2631G>T ORCA-IN 11 67018132 67018132 single base substitution G T upstream_gene_variant OV-AU 11 66885100 66885100 single base substitution A T upstream_gene_variant OV-AU 11 66887662 66887662 single base substitution T C intron_variant OV-AU 11 66891061 66891061 single base substitution T C intron_variant OV-AU 11 66896718 66896718 single base substitution G A intron_variant OV-AU 11 66908941 66908941 single base substitution T G intron_variant OV-AU 11 66918404 66918404 single base substitution G C downstream_gene_variant OV-AU 11 66918404 66918404 single base substitution G C intron_variant OV-AU 11 66919444 66919444 single base substitution T G downstream_gene_variant OV-AU 11 66919444 66919444 single base substitution T G intron_variant OV-AU 11 66920026 66920026 single base substitution C G downstream_gene_variant OV-AU 11 66920026 66920026 single base substitution C G intron_variant OV-AU 11 66926080 66926080 single base substitution C G intron_variant OV-AU 11 66930128 66930128 single base substitution C T intron_variant OV-AU 11 66938762 66938762 single base substitution G A intron_variant OV-AU 11 66941619 66941619 single base substitution C G intron_variant OV-AU 11 66946037 66946037 single base substitution G A intron_variant OV-AU 11 66957030 66957030 single base substitution G A intron_variant OV-AU 11 66962874 66962874 single base substitution A C intron_variant OV-AU 11 66968047 66968047 single base substitution A G intron_variant OV-AU 11 66969204 66969204 single base substitution A T intron_variant OV-AU 11 66970246 66970246 single base substitution C A intron_variant OV-AU 11 66970246 66970246 single base substitution C A upstream_gene_variant OV-AU 11 66977431 66977431 single base substitution C T intron_variant OV-AU 11 66983119 66983119 single base substitution A C exon_variant OV-AU 11 66983119 66983119 single base substitution A C intron_variant OV-AU 11 66983119 66983119 single base substitution A C upstream_gene_variant OV-AU 11 66985671 66985671 single base substitution G C downstream_gene_variant OV-AU 11 66985671 66985671 single base substitution G C intron_variant OV-AU 11 66986076 66986076 single base substitution A G downstream_gene_variant OV-AU 11 66986076 66986076 single base substitution A G intron_variant OV-AU 11 66992595 66992595 single base substitution G A intron_variant OV-AU 11 67000353 67000353 single base substitution A G intron_variant OV-AU 11 67000361 67000361 single base substitution G A intron_variant OV-AU 11 67005479 67005479 single base substitution T C intron_variant OV-AU 11 67005479 67005479 single base substitution T C upstream_gene_variant OV-AU 11 67007963 67007963 single base substitution T C intron_variant OV-AU 11 67007963 67007963 single base substitution T C upstream_gene_variant OV-AU 11 67011598 67011598 single base substitution A G downstream_gene_variant OV-AU 11 67011598 67011598 single base substitution A G intron_variant OV-AU 11 67011598 67011598 single base substitution A G upstream_gene_variant OV-US 11 67017881 67017881 single base substitution A C downstream_gene_variant OV-US 11 67017881 67017881 single base substitution A C exon_variant OV-US 11 67017881 67017881 single base substitution A C intron_variant OV-US 11 67017881 67017881 single base substitution A C missense_variant I252L 754A>C OV-US 11 67017881 67017881 single base substitution A C missense_variant I355L 1063A>C OV-US 11 67017881 67017881 single base substitution A C missense_variant I794L 2380A>C OV-US 11 67017881 67017881 single base substitution A C upstream_gene_variant OV-US 11 67022386 67022386 single base substitution C T 3_prime_UTR_variant OV-US 11 67022386 67022386 single base substitution C T exon_variant OV-US 11 67022386 67022386 single base substitution C T missense_variant R1117C 3349C>T OV-US 11 67022386 67022386 single base substitution C T missense_variant R575C 1723C>T OV-US 11 67022386 67022386 single base substitution C T missense_variant R678C 2032C>T PACA-AU 11 66884196 66884196 single base substitution C T upstream_gene_variant PACA-AU 11 66889785 66889785 single base substitution A G intron_variant PACA-AU 11 66890208 66890208 single base substitution G A intron_variant PACA-AU 11 66895178 66895178 single base substitution T A intron_variant PACA-AU 11 66896953 66896953 single base substitution C T intron_variant PACA-AU 11 66902551 66902551 deletion of <=200bp C - intron_variant PACA-AU 11 66904973 66904973 single base substitution A G intron_variant PACA-AU 11 66911084 66911084 single base substitution T C intron_variant PACA-AU 11 66937575 66937575 single base substitution T C intron_variant PACA-AU 11 66941106 66941106 single base substitution C T intron_variant PACA-AU 11 66946266 66946266 single base substitution G A intron_variant PACA-AU 11 66947886 66947886 single base substitution G A exon_variant PACA-AU 11 66947886 66947886 single base substitution G A intron_variant PACA-AU 11 66948913 66948913 single base substitution C T downstream_gene_variant PACA-AU 11 66948913 66948913 single base substitution C T intron_variant PACA-AU 11 66949364 66949364 single base substitution G T downstream_gene_variant PACA-AU 11 66949364 66949364 single base substitution G T splice_donor_variant PACA-AU 11 66950365 66950365 single base substitution T C downstream_gene_variant PACA-AU 11 66950365 66950365 single base substitution T C intron_variant PACA-AU 11 66955015 66955015 single base substitution T C intron_variant PACA-AU 11 66955017 66955017 single base substitution G T intron_variant PACA-AU 11 66955201 66955201 single base substitution C T intron_variant PACA-AU 11 66955422 66955422 single base substitution T C intron_variant PACA-AU 11 66960522 66960522 single base substitution G A intron_variant PACA-AU 11 66963318 66963318 single base substitution G A intron_variant PACA-AU 11 66964556 66964556 single base substitution A T intron_variant PACA-AU 11 66965365 66965365 single base substitution A G intron_variant PACA-AU 11 66968111 66968111 single base substitution T G intron_variant PACA-AU 11 66968687 66968687 single base substitution A G intron_variant PACA-AU 11 66970300 66970300 single base substitution C T intron_variant PACA-AU 11 66970300 66970300 single base substitution C T upstream_gene_variant PACA-AU 11 66973999 66973999 single base substitution G A intron_variant PACA-AU 11 66973999 66973999 single base substitution G A upstream_gene_variant PACA-AU 11 66974300 66974300 single base substitution C G intron_variant PACA-AU 11 66974300 66974300 single base substitution C G upstream_gene_variant PACA-AU 11 66982539 66982539 single base substitution C G intron_variant PACA-AU 11 66982539 66982539 single base substitution C G upstream_gene_variant PACA-AU 11 66996718 66996718 single base substitution T G intron_variant PACA-AU 11 66996718 66996718 single base substitution T G upstream_gene_variant PACA-AU 11 67000391 67000391 single base substitution G A intron_variant PACA-AU 11 67004242 67004242 insertion of <=200bp - A intron_variant PACA-AU 11 67004242 67004242 insertion of <=200bp - A upstream_gene_variant PACA-AU 11 67005838 67005838 single base substitution C T intron_variant PACA-AU 11 67005838 67005838 single base substitution C T upstream_gene_variant PACA-AU 11 67011029 67011029 single base substitution A T exon_variant PACA-AU 11 67011029 67011029 single base substitution A T intron_variant PACA-AU 11 67011029 67011029 single base substitution A T upstream_gene_variant PACA-AU 11 67017866 67017866 single base substitution G T downstream_gene_variant PACA-AU 11 67017866 67017866 single base substitution G T exon_variant PACA-AU 11 67017866 67017866 single base substitution G T intron_variant PACA-AU 11 67017866 67017866 single base substitution G T missense_variant V247F 739G>T PACA-AU 11 67017866 67017866 single base substitution G T missense_variant V350F 1048G>T PACA-AU 11 67017866 67017866 single base substitution G T missense_variant V789F 2365G>T PACA-AU 11 67017866 67017866 single base substitution G T upstream_gene_variant PACA-AU 11 67030205 67030205 single base substitution T G downstream_gene_variant PACA-AU 11 67030317 67030317 single base substitution C A downstream_gene_variant PACA-CA 11 66892812 66892812 single base substitution T G intron_variant PACA-CA 11 66895178 66895178 single base substitution T A intron_variant PACA-CA 11 66897001 66897001 single base substitution C T intron_variant PACA-CA 11 66899545 66899545 single base substitution G A intron_variant PACA-CA 11 66900128 66900128 single base substitution G A intron_variant PACA-CA 11 66900163 66900163 single base substitution T C intron_variant PACA-CA 11 66902277 66902277 single base substitution T A intron_variant PACA-CA 11 66904052 66904052 single base substitution G A intron_variant PACA-CA 11 66905483 66905483 single base substitution A T intron_variant PACA-CA 11 66912785 66912785 single base substitution G A intron_variant PACA-CA 11 66916523 66916523 single base substitution C A intron_variant PACA-CA 11 66917340 66917340 single base substitution C T downstream_gene_variant PACA-CA 11 66917340 66917340 single base substitution C T intron_variant PACA-CA 11 66918126 66918126 single base substitution G T downstream_gene_variant PACA-CA 11 66918126 66918126 single base substitution G T intron_variant PACA-CA 11 66922129 66922129 single base substitution C T intron_variant PACA-CA 11 66924292 66924292 single base substitution G A intron_variant PACA-CA 11 66927499 66927499 single base substitution C G intron_variant PACA-CA 11 66931964 66931964 single base substitution T G intron_variant PACA-CA 11 66932358 66932358 single base substitution C G intron_variant PACA-CA 11 66936794 66936794 single base substitution G C intron_variant PACA-CA 11 66937110 66937110 single base substitution G T intron_variant PACA-CA 11 66937507 66937507 single base substitution G A intron_variant PACA-CA 11 66940678 66940678 single base substitution C G intron_variant PACA-CA 11 66941999 66941999 single base substitution T A intron_variant PACA-CA 11 66956853 66956853 single base substitution G A intron_variant PACA-CA 11 66957333 66957333 single base substitution C G intron_variant PACA-CA 11 66959577 66959577 single base substitution T C intron_variant PACA-CA 11 66960626 66960626 single base substitution C T intron_variant PACA-CA 11 66964302 66964302 single base substitution A C intron_variant PACA-CA 11 66965184 66965184 single base substitution G A intron_variant PACA-CA 11 66965960 66965960 single base substitution G A intron_variant PACA-CA 11 66967683 66967683 single base substitution G A intron_variant PACA-CA 11 66968504 66968504 single base substitution A G intron_variant PACA-CA 11 66968707 66968707 single base substitution A G intron_variant PACA-CA 11 66968932 66968932 single base substitution G T intron_variant PACA-CA 11 66969427 66969427 deletion of <=200bp A - intron_variant PACA-CA 11 66972200 66972200 single base substitution G C intron_variant PACA-CA 11 66972200 66972200 single base substitution G C upstream_gene_variant PACA-CA 11 66975305 66975305 single base substitution G T intron_variant PACA-CA 11 66975423 66975423 single base substitution G T intron_variant PACA-CA 11 66979539 66979539 single base substitution G A intron_variant PACA-CA 11 66979539 66979539 single base substitution G A upstream_gene_variant PACA-CA 11 66981503 66981503 single base substitution T A intron_variant PACA-CA 11 66981503 66981503 single base substitution T A upstream_gene_variant PACA-CA 11 66981862 66981862 single base substitution A C intron_variant PACA-CA 11 66981862 66981862 single base substitution A C upstream_gene_variant PACA-CA 11 66984415 66984415 single base substitution C A downstream_gene_variant PACA-CA 11 66984415 66984415 single base substitution C A intron_variant PACA-CA 11 66984415 66984415 single base substitution C A upstream_gene_variant PACA-CA 11 66985342 66985342 single base substitution C T downstream_gene_variant PACA-CA 11 66985342 66985342 single base substitution C T exon_variant PACA-CA 11 66985342 66985342 single base substitution C T synonymous_variant F276F 828C>T PACA-CA 11 66986414 66986414 single base substitution C A downstream_gene_variant PACA-CA 11 66986414 66986414 single base substitution C A intron_variant PACA-CA 11 66991075 66991075 single base substitution T A downstream_gene_variant PACA-CA 11 66991075 66991075 single base substitution T A intron_variant PACA-CA 11 66994548 66994548 deletion of <=200bp A - intron_variant PACA-CA 11 66994548 66994548 deletion of <=200bp A - upstream_gene_variant PACA-CA 11 66995701 66995701 single base substitution C G intron_variant PACA-CA 11 66995701 66995701 single base substitution C G upstream_gene_variant PACA-CA 11 66997974 66997974 single base substitution C A intron_variant PACA-CA 11 66997974 66997974 single base substitution C A upstream_gene_variant PACA-CA 11 66999222 66999222 single base substitution G T exon_variant PACA-CA 11 66999222 66999222 single base substitution G T missense_variant D424Y 1270G>T PACA-CA 11 66999222 66999222 single base substitution G T upstream_gene_variant PACA-CA 11 67001625 67001625 single base substitution T G intron_variant PACA-CA 11 67003076 67003085 deletion of <=200bp TTTTGTTTTG - intron_variant PACA-CA 11 67003076 67003085 deletion of <=200bp TTTTGTTTTG - upstream_gene_variant PACA-CA 11 67003287 67003287 single base substitution C T intron_variant PACA-CA 11 67003287 67003287 single base substitution C T upstream_gene_variant PACA-CA 11 67004929 67004929 single base substitution C T intron_variant PACA-CA 11 67004929 67004929 single base substitution C T upstream_gene_variant PACA-CA 11 67005793 67005793 single base substitution G A intron_variant PACA-CA 11 67005793 67005793 single base substitution G A upstream_gene_variant PACA-CA 11 67008728 67008728 single base substitution C T intron_variant PACA-CA 11 67008728 67008728 single base substitution C T upstream_gene_variant PACA-CA 11 67012289 67012289 single base substitution T G downstream_gene_variant PACA-CA 11 67012289 67012289 single base substitution T G intron_variant PACA-CA 11 67012289 67012289 single base substitution T G upstream_gene_variant PACA-CA 11 67012811 67012811 single base substitution G A downstream_gene_variant PACA-CA 11 67012811 67012811 single base substitution G A exon_variant PACA-CA 11 67012811 67012811 single base substitution G A missense_variant R133Q 398G>A PACA-CA 11 67012811 67012811 single base substitution G A missense_variant R30Q 89G>A PACA-CA 11 67012811 67012811 single base substitution G A missense_variant R572Q 1715G>A PACA-CA 11 67012811 67012811 single base substitution G A upstream_gene_variant PACA-CA 11 67018892 67018892 insertion of <=200bp - A downstream_gene_variant PACA-CA 11 67018892 67018892 insertion of <=200bp - A intron_variant PACA-CA 11 67018892 67018892 insertion of <=200bp - A upstream_gene_variant PAEN-AU 11 66952313 66952313 single base substitution C T downstream_gene_variant PAEN-AU 11 66952313 66952313 single base substitution C T intron_variant PAEN-IT 11 66898366 66898366 single base substitution G A intron_variant PAEN-IT 11 66901642 66901642 single base substitution G T intron_variant PAEN-IT 11 66973003 66973003 single base substitution A G intron_variant PAEN-IT 11 66973003 66973003 single base substitution A G upstream_gene_variant PAEN-IT 11 66974565 66974565 single base substitution C T intron_variant PAEN-IT 11 66974565 66974565 single base substitution C T upstream_gene_variant PAEN-IT 11 67013978 67013978 single base substitution A G downstream_gene_variant PAEN-IT 11 67013978 67013978 single base substitution A G intron_variant PBCA-DE 11 66883829 66883829 single base substitution G T upstream_gene_variant PBCA-DE 11 66890635 66890635 single base substitution C T intron_variant PBCA-DE 11 66895432 66895432 single base substitution C T intron_variant PBCA-DE 11 66901522 66901522 single base substitution T A intron_variant PBCA-DE 11 66903124 66903124 single base substitution G A intron_variant PBCA-DE 11 66904022 66904022 single base substitution G T intron_variant PBCA-DE 11 66957678 66957678 single base substitution C T intron_variant PBCA-DE 11 66989426 66989426 single base substitution A G downstream_gene_variant PBCA-DE 11 66989426 66989426 single base substitution A G intron_variant PBCA-DE 11 67000224 67000224 single base substitution G A intron_variant PBCA-DE 11 67001047 67001047 insertion of <=200bp - CAG intron_variant PBCA-DE 11 67006531 67006531 single base substitution G A intron_variant PBCA-DE 11 67006531 67006531 single base substitution G A upstream_gene_variant PBCA-DE 11 67025924 67025925 deletion of <=200bp TG - downstream_gene_variant PRAD-CA 11 66892658 66892658 single base substitution C T intron_variant PRAD-CA 11 66902561 66902561 single base substitution C T intron_variant PRAD-CA 11 66917094 66917094 single base substitution C T downstream_gene_variant PRAD-CA 11 66917094 66917094 single base substitution C T intron_variant PRAD-CA 11 66943388 66943388 single base substitution T C intron_variant PRAD-CA 11 66990893 66990893 single base substitution A G downstream_gene_variant PRAD-CA 11 66990893 66990893 single base substitution A G intron_variant PRAD-UK 11 66883129 66883129 single base substitution C T upstream_gene_variant PRAD-UK 11 66895993 66895993 deletion of <=200bp T - intron_variant PRAD-UK 11 66896687 66896687 single base substitution C T intron_variant PRAD-UK 11 66898127 66898128 deletion of <=200bp CT - intron_variant PRAD-UK 11 66929937 66929937 single base substitution G A intron_variant PRAD-UK 11 66937578 66937581 deletion of <=200bp GAAG - intron_variant PRAD-UK 11 66952174 66952174 single base substitution G A downstream_gene_variant PRAD-UK 11 66952174 66952174 single base substitution G A intron_variant PRAD-UK 11 66963558 66963558 single base substitution C G intron_variant PRAD-UK 11 66966553 66966553 single base substitution T G intron_variant PRAD-UK 11 66973031 66973031 single base substitution C T intron_variant PRAD-UK 11 66973031 66973031 single base substitution C T upstream_gene_variant PRAD-UK 11 66983984 66983984 single base substitution A G downstream_gene_variant PRAD-UK 11 66983984 66983984 single base substitution A G intron_variant PRAD-UK 11 66983984 66983984 single base substitution A G upstream_gene_variant PRAD-UK 11 66984674 66984674 single base substitution C T downstream_gene_variant PRAD-UK 11 66984674 66984674 single base substitution C T intron_variant PRAD-UK 11 66984674 66984674 single base substitution C T upstream_gene_variant PRAD-UK 11 66985145 66985145 single base substitution G A downstream_gene_variant PRAD-UK 11 66985145 66985145 single base substitution G A exon_variant PRAD-UK 11 66985145 66985145 single base substitution G A intron_variant PRAD-UK 11 66988655 66988655 single base substitution A G downstream_gene_variant PRAD-UK 11 66988655 66988655 single base substitution A G intron_variant PRAD-UK 11 66996327 66996327 single base substitution A T intron_variant PRAD-UK 11 66996327 66996327 single base substitution A T upstream_gene_variant PRAD-UK 11 67014841 67014841 single base substitution G T downstream_gene_variant PRAD-UK 11 67014841 67014841 single base substitution G T intron_variant PRAD-UK 11 67014841 67014841 single base substitution G T upstream_gene_variant PRAD-UK 11 67022728 67022728 single base substitution G A 3_prime_UTR_variant PRAD-UK 11 67022728 67022728 single base substitution G A exon_variant PRAD-US 11 66999361 66999361 single base substitution C A exon_variant PRAD-US 11 66999361 66999361 single base substitution C A missense_variant S470Y 1409C>A PRAD-US 11 67017956 67017956 single base substitution C A downstream_gene_variant PRAD-US 11 67017956 67017956 single base substitution C A exon_variant PRAD-US 11 67017956 67017956 single base substitution C A intron_variant PRAD-US 11 67017956 67017956 single base substitution C A missense_variant L277M 829C>A PRAD-US 11 67017956 67017956 single base substitution C A missense_variant L380M 1138C>A PRAD-US 11 67017956 67017956 single base substitution C A missense_variant L819M 2455C>A PRAD-US 11 67017956 67017956 single base substitution C A upstream_gene_variant RECA-EU 11 66891059 66891059 single base substitution T C intron_variant RECA-EU 11 66891329 66891329 single base substitution G C intron_variant RECA-EU 11 66903436 66903436 single base substitution G T intron_variant RECA-EU 11 66905864 66905864 single base substitution T G intron_variant RECA-EU 11 66907905 66907905 single base substitution A G intron_variant RECA-EU 11 66915243 66915243 single base substitution G A intron_variant RECA-EU 11 66934119 66934119 single base substitution C T intron_variant RECA-EU 11 66948918 66948918 single base substitution C A downstream_gene_variant RECA-EU 11 66948918 66948918 single base substitution C A intron_variant RECA-EU 11 66957517 66957517 single base substitution A T intron_variant RECA-EU 11 66962484 66962484 single base substitution G T intron_variant RECA-EU 11 66964977 66964977 single base substitution A G intron_variant RECA-EU 11 66966786 66966786 single base substitution C A intron_variant RECA-EU 11 66983322 66983322 single base substitution G A downstream_gene_variant RECA-EU 11 66983322 66983322 single base substitution G A splice_region_variant RECA-EU 11 66983322 66983322 single base substitution G A upstream_gene_variant RECA-EU 11 66983377 66983377 single base substitution T C downstream_gene_variant RECA-EU 11 66983377 66983377 single base substitution T C exon_variant RECA-EU 11 66983377 66983377 single base substitution T C missense_variant F215S 644T>C RECA-EU 11 66983377 66983377 single base substitution T C upstream_gene_variant RECA-EU 11 66992914 66992914 single base substitution C A intron_variant RECA-EU 11 67005079 67005079 single base substitution T A intron_variant RECA-EU 11 67005079 67005079 single base substitution T A upstream_gene_variant RECA-EU 11 67008636 67008636 single base substitution A G intron_variant RECA-EU 11 67008636 67008636 single base substitution A G upstream_gene_variant RECA-EU 11 67015788 67015788 single base substitution A C downstream_gene_variant RECA-EU 11 67015788 67015788 single base substitution A C exon_variant RECA-EU 11 67015788 67015788 single base substitution A C missense_variant N126H 376A>C RECA-EU 11 67015788 67015788 single base substitution A C missense_variant N229H 685A>C RECA-EU 11 67015788 67015788 single base substitution A C missense_variant N668H 2002A>C RECA-EU 11 67015788 67015788 single base substitution A C upstream_gene_variant RECA-EU 11 67020457 67020457 single base substitution G A downstream_gene_variant RECA-EU 11 67020457 67020457 single base substitution G A intron_variant RECA-EU 11 67023338 67023338 single base substitution T C 3_prime_UTR_variant RECA-EU 11 67023338 67023338 single base substitution T C exon_variant RECA-EU 11 67029652 67029652 single base substitution C A downstream_gene_variant SKCA-BR 11 66882765 66882765 single base substitution A G upstream_gene_variant SKCA-BR 11 66882788 66882788 single base substitution G T upstream_gene_variant SKCA-BR 11 66882809 66882809 single base substitution T G upstream_gene_variant SKCA-BR 11 66883187 66883187 single base substitution T G upstream_gene_variant SKCA-BR 11 66890114 66890114 insertion of <=200bp - TTTTA intron_variant SKCA-BR 11 66890831 66890831 single base substitution C T intron_variant SKCA-BR 11 66892184 66892184 single base substitution C T intron_variant SKCA-BR 11 66894950 66894950 single base substitution T A intron_variant SKCA-BR 11 66898596 66898596 single base substitution G A intron_variant SKCA-BR 11 66900695 66900695 single base substitution C T intron_variant SKCA-BR 11 66904310 66904310 single base substitution C T intron_variant SKCA-BR 11 66907944 66907944 single base substitution C T intron_variant SKCA-BR 11 66909310 66909310 single base substitution C T intron_variant SKCA-BR 11 66918956 66918956 single base substitution G A downstream_gene_variant SKCA-BR 11 66918956 66918956 single base substitution G A intron_variant SKCA-BR 11 66924349 66924349 single base substitution T G intron_variant SKCA-BR 11 66926142 66926142 single base substitution T A intron_variant SKCA-BR 11 66933410 66933410 single base substitution A C intron_variant SKCA-BR 11 66933662 66933662 single base substitution T A intron_variant SKCA-BR 11 66933890 66933890 single base substitution C A intron_variant SKCA-BR 11 66936069 66936069 single base substitution C T intron_variant SKCA-BR 11 66937229 66937230 deletion of <=200bp TC - intron_variant SKCA-BR 11 66937871 66937871 single base substitution C T intron_variant SKCA-BR 11 66939659 66939659 single base substitution T G intron_variant SKCA-BR 11 66941587 66941587 single base substitution G A intron_variant SKCA-BR 11 66943815 66943815 single base substitution C G intron_variant SKCA-BR 11 66943830 66943830 single base substitution C A intron_variant SKCA-BR 11 66943844 66943844 single base substitution C T intron_variant SKCA-BR 11 66943854 66943854 single base substitution T C intron_variant SKCA-BR 11 66943863 66943863 single base substitution C G intron_variant SKCA-BR 11 66948982 66948982 single base substitution C T downstream_gene_variant SKCA-BR 11 66948982 66948982 single base substitution C T intron_variant SKCA-BR 11 66950001 66950002 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 11 66950001 66950002 deletion of <=200bp CT - intron_variant SKCA-BR 11 66961457 66961457 single base substitution G T intron_variant SKCA-BR 11 66962656 66962656 single base substitution C T intron_variant SKCA-BR 11 66964086 66964086 single base substitution A C intron_variant SKCA-BR 11 66964152 66964152 single base substitution C T intron_variant SKCA-BR 11 66965494 66965533 deletion of <=200bp ATTTGTTTACTATTAAGATTGAAAATATATTTACTATCTT - intron_variant SKCA-BR 11 66965604 66965604 single base substitution A G intron_variant SKCA-BR 11 66965815 66965815 single base substitution G T intron_variant SKCA-BR 11 66966230 66966235 deletion of <=200bp GTTTGT - intron_variant SKCA-BR 11 66966493 66966493 single base substitution A C intron_variant SKCA-BR 11 66967649 66967649 single base substitution C T intron_variant SKCA-BR 11 66968315 66968315 single base substitution C T intron_variant SKCA-BR 11 66969358 66969358 single base substitution C T intron_variant SKCA-BR 11 66969801 66969801 single base substitution G A intron_variant SKCA-BR 11 66970597 66970597 single base substitution A G intron_variant SKCA-BR 11 66970597 66970597 single base substitution A G upstream_gene_variant SKCA-BR 11 66971526 66971526 single base substitution C T intron_variant SKCA-BR 11 66971526 66971526 single base substitution C T upstream_gene_variant SKCA-BR 11 66975070 66975070 single base substitution C T exon_variant SKCA-BR 11 66975070 66975070 single base substitution C T missense_variant P133S 397C>T SKCA-BR 11 66975070 66975070 single base substitution C T upstream_gene_variant SKCA-BR 11 66976083 66976083 single base substitution A T intron_variant SKCA-BR 11 66978909 66978909 single base substitution A C intron_variant SKCA-BR 11 66978909 66978909 single base substitution A C upstream_gene_variant SKCA-BR 11 66982442 66982442 single base substitution G A intron_variant SKCA-BR 11 66982442 66982442 single base substitution G A upstream_gene_variant SKCA-BR 11 66989551 66989551 single base substitution A T downstream_gene_variant SKCA-BR 11 66989551 66989551 single base substitution A T intron_variant SKCA-BR 11 66989556 66989556 single base substitution A T downstream_gene_variant SKCA-BR 11 66989556 66989556 single base substitution A T intron_variant SKCA-BR 11 66995154 66995154 single base substitution C T intron_variant SKCA-BR 11 66995154 66995154 single base substitution C T upstream_gene_variant SKCA-BR 11 67001035 67001035 single base substitution A G intron_variant SKCA-BR 11 67006095 67006095 single base substitution C T intron_variant SKCA-BR 11 67006095 67006095 single base substitution C T upstream_gene_variant SKCA-BR 11 67008739 67008739 single base substitution A C intron_variant SKCA-BR 11 67008739 67008739 single base substitution A C upstream_gene_variant SKCA-BR 11 67014314 67014314 single base substitution T A downstream_gene_variant SKCA-BR 11 67014314 67014314 single base substitution T A intron_variant SKCA-BR 11 67014508 67014510 deletion of <=200bp TTA - downstream_gene_variant SKCA-BR 11 67014508 67014510 deletion of <=200bp TTA - intron_variant SKCA-BR 11 67014539 67014542 deletion of <=200bp TATA - downstream_gene_variant SKCA-BR 11 67014539 67014542 deletion of <=200bp TATA - intron_variant SKCA-BR 11 67021891 67021891 single base substitution T G splice_donor_variant SKCA-BR 11 67021928 67021928 single base substitution T C intron_variant SKCA-BR 11 67027683 67027683 single base substitution A G downstream_gene_variant SKCM-US 11 66948824 66948824 single base substitution T A downstream_gene_variant SKCM-US 11 66948824 66948824 single base substitution T A stop_gained L72* 215T>A SKCM-US 11 66999061 66999061 single base substitution C T exon_variant SKCM-US 11 66999061 66999061 single base substitution C T missense_variant S370F 1109C>T SKCM-US 11 66999061 66999061 single base substitution C T upstream_gene_variant SKCM-US 11 66999121 66999121 single base substitution C T exon_variant SKCM-US 11 66999121 66999121 single base substitution C T missense_variant S390F 1169C>T SKCM-US 11 66999121 66999121 single base substitution C T upstream_gene_variant SKCM-US 11 67012770 67012770 single base substitution C T downstream_gene_variant SKCM-US 11 67012770 67012770 single base substitution C T exon_variant SKCM-US 11 67012770 67012770 single base substitution C T synonymous_variant S119S 357C>T SKCM-US 11 67012770 67012770 single base substitution C T synonymous_variant S16S 48C>T SKCM-US 11 67012770 67012770 single base substitution C T synonymous_variant S558S 1674C>T SKCM-US 11 67012770 67012770 single base substitution C T upstream_gene_variant SKCM-US 11 67012810 67012810 single base substitution C T downstream_gene_variant SKCM-US 11 67012810 67012810 single base substitution C T exon_variant SKCM-US 11 67012810 67012810 single base substitution C T stop_gained R133* 397C>T SKCM-US 11 67012810 67012810 single base substitution C T stop_gained R30* 88C>T SKCM-US 11 67012810 67012810 single base substitution C T stop_gained R572* 1714C>T SKCM-US 11 67012810 67012810 single base substitution C T upstream_gene_variant SKCM-US 11 67017891 67017891 single base substitution C T downstream_gene_variant SKCM-US 11 67017891 67017891 single base substitution C T exon_variant SKCM-US 11 67017891 67017891 single base substitution C T intron_variant SKCM-US 11 67017891 67017891 single base substitution C T missense_variant S255L 764C>T SKCM-US 11 67017891 67017891 single base substitution C T missense_variant S358L 1073C>T SKCM-US 11 67017891 67017891 single base substitution C T missense_variant S797L 2390C>T SKCM-US 11 67017891 67017891 single base substitution C T upstream_gene_variant SKCM-US 11 67020215 67020215 single base substitution C T 3_prime_UTR_variant SKCM-US 11 67020215 67020215 single base substitution C T downstream_gene_variant SKCM-US 11 67020215 67020215 single base substitution C T exon_variant SKCM-US 11 67020215 67020215 single base substitution C T missense_variant A398V 1193C>T SKCM-US 11 67020215 67020215 single base substitution C T missense_variant A501V 1502C>T SKCM-US 11 67020215 67020215 single base substitution C T missense_variant A940V 2819C>T SKCM-US 11 67020265 67020265 single base substitution C T 3_prime_UTR_variant SKCM-US 11 67020265 67020265 single base substitution C T downstream_gene_variant SKCM-US 11 67020265 67020265 single base substitution C T exon_variant SKCM-US 11 67020265 67020265 single base substitution C T missense_variant L415F 1243C>T SKCM-US 11 67020265 67020265 single base substitution C T missense_variant L518F 1552C>T SKCM-US 11 67020265 67020265 single base substitution C T missense_variant L957F 2869C>T SKCM-US 11 67022482 67022482 single base substitution C T 3_prime_UTR_variant SKCM-US 11 67022482 67022482 single base substitution C T exon_variant SKCM-US 11 67022482 67022482 single base substitution C T missense_variant L1149F 3445C>T SKCM-US 11 67022482 67022482 single base substitution C T missense_variant L607F 1819C>T SKCM-US 11 67022482 67022482 single base substitution C T missense_variant L710F 2128C>T STAD-US 11 66999252 66999252 single base substitution C T exon_variant STAD-US 11 66999252 66999252 single base substitution C T missense_variant H434Y 1300C>T STAD-US 11 67010480 67010480 single base substitution A G intron_variant STAD-US 11 67010480 67010480 single base substitution A G missense_variant I494V 1480A>G STAD-US 11 67010480 67010480 single base substitution A G missense_variant I55V 163A>G STAD-US 11 67010480 67010480 single base substitution A G splice_region_variant STAD-US 11 67010480 67010480 single base substitution A G upstream_gene_variant STAD-US 11 67017751 67017751 single base substitution T C downstream_gene_variant STAD-US 11 67017751 67017751 single base substitution T C exon_variant STAD-US 11 67017751 67017751 single base substitution T C synonymous_variant S208S 624T>C STAD-US 11 67017751 67017751 single base substitution T C synonymous_variant S311S 933T>C STAD-US 11 67017751 67017751 single base substitution T C synonymous_variant S750S 2250T>C STAD-US 11 67017751 67017751 single base substitution T C upstream_gene_variant STAD-US 11 67017889 67017889 single base substitution A T downstream_gene_variant STAD-US 11 67017889 67017889 single base substitution A T exon_variant STAD-US 11 67017889 67017889 single base substitution A T intron_variant STAD-US 11 67017889 67017889 single base substitution A T synonymous_variant G254G 762A>T STAD-US 11 67017889 67017889 single base substitution A T synonymous_variant G357G 1071A>T STAD-US 11 67017889 67017889 single base substitution A T synonymous_variant G796G 2388A>T STAD-US 11 67017889 67017889 single base substitution A T upstream_gene_variant STAD-US 11 67018078 67018078 single base substitution A G downstream_gene_variant STAD-US 11 67018078 67018078 single base substitution A G exon_variant STAD-US 11 67018078 67018078 single base substitution A G intron_variant STAD-US 11 67018078 67018078 single base substitution A G synonymous_variant E317E 951A>G STAD-US 11 67018078 67018078 single base substitution A G synonymous_variant E420E 1260A>G STAD-US 11 67018078 67018078 single base substitution A G synonymous_variant E859E 2577A>G STAD-US 11 67018078 67018078 single base substitution A G upstream_gene_variant STAD-US 11 67018168 67018168 single base substitution C T downstream_gene_variant STAD-US 11 67018168 67018168 single base substitution C T exon_variant STAD-US 11 67018168 67018168 single base substitution C T intron_variant STAD-US 11 67018168 67018168 single base substitution C T synonymous_variant D347D 1041C>T STAD-US 11 67018168 67018168 single base substitution C T synonymous_variant D450D 1350C>T STAD-US 11 67018168 67018168 single base substitution C T synonymous_variant D889D 2667C>T STAD-US 11 67018168 67018168 single base substitution C T upstream_gene_variant STAD-US 11 67018182 67018182 single base substitution A G downstream_gene_variant STAD-US 11 67018182 67018182 single base substitution A G exon_variant STAD-US 11 67018182 67018182 single base substitution A G intron_variant STAD-US 11 67018182 67018182 single base substitution A G missense_variant Q352R 1055A>G STAD-US 11 67018182 67018182 single base substitution A G missense_variant Q455R 1364A>G STAD-US 11 67018182 67018182 single base substitution A G missense_variant Q894R 2681A>G STAD-US 11 67018182 67018182 single base substitution A G upstream_gene_variant STAD-US 11 67018208 67018208 single base substitution C T downstream_gene_variant STAD-US 11 67018208 67018208 single base substitution C T exon_variant STAD-US 11 67018208 67018208 single base substitution C T intron_variant STAD-US 11 67018208 67018208 single base substitution C T missense_variant R361C 1081C>T STAD-US 11 67018208 67018208 single base substitution C T missense_variant R464C 1390C>T STAD-US 11 67018208 67018208 single base substitution C T missense_variant R903C 2707C>T STAD-US 11 67018208 67018208 single base substitution C T upstream_gene_variant STAD-US 11 67020972 67020972 single base substitution C T 3_prime_UTR_variant STAD-US 11 67020972 67020972 single base substitution C T downstream_gene_variant STAD-US 11 67020972 67020972 single base substitution C T exon_variant STAD-US 11 67020972 67020972 single base substitution C T missense_variant A452V 1355C>T STAD-US 11 67020972 67020972 single base substitution C T missense_variant A555V 1664C>T STAD-US 11 67020972 67020972 single base substitution C T missense_variant A994V 2981C>T STAD-US 11 67021038 67021038 single base substitution A G 3_prime_UTR_variant STAD-US 11 67021038 67021038 single base substitution A G downstream_gene_variant STAD-US 11 67021038 67021038 single base substitution A G exon_variant STAD-US 11 67021038 67021038 single base substitution A G missense_variant D1016G 3047A>G STAD-US 11 67021038 67021038 single base substitution A G missense_variant D474G 1421A>G STAD-US 11 67021038 67021038 single base substitution A G missense_variant D577G 1730A>G STAD-US 11 67021875 67021875 single base substitution A G 3_prime_UTR_variant STAD-US 11 67021875 67021875 single base substitution A G exon_variant STAD-US 11 67021875 67021875 single base substitution A G missense_variant E1098G 3293A>G STAD-US 11 67021875 67021875 single base substitution A G missense_variant E556G 1667A>G STAD-US 11 67021875 67021875 single base substitution A G missense_variant E659G 1976A>G STAD-US 11 67021880 67021880 single base substitution A G 3_prime_UTR_variant STAD-US 11 67021880 67021880 single base substitution A G exon_variant STAD-US 11 67021880 67021880 single base substitution A G missense_variant N1100D 3298A>G STAD-US 11 67021880 67021880 single base substitution A G missense_variant N558D 1672A>G STAD-US 11 67021880 67021880 single base substitution A G missense_variant N661D 1981A>G STAD-US 11 67022389 67022389 single base substitution A G 3_prime_UTR_variant STAD-US 11 67022389 67022389 single base substitution A G exon_variant STAD-US 11 67022389 67022389 single base substitution A G missense_variant I1118V 3352A>G STAD-US 11 67022389 67022389 single base substitution A G missense_variant I576V 1726A>G STAD-US 11 67022389 67022389 single base substitution A G missense_variant I679V 2035A>G THCA-US 11 66995593 66995593 deletion of <=200bp C - exon_variant THCA-US 11 66995593 66995593 deletion of <=200bp C - frameshift_variant S348 THCA-US 11 66995593 66995593 deletion of <=200bp C - upstream_gene_variant THCA-US 11 67012703 67012703 single base substitution C T 5_prime_UTR_variant THCA-US 11 67012703 67012703 single base substitution C T downstream_gene_variant THCA-US 11 67012703 67012703 single base substitution C T exon_variant THCA-US 11 67012703 67012703 single base substitution C T missense_variant P536L 1607C>T THCA-US 11 67012703 67012703 single base substitution C T missense_variant P97L 290C>T THCA-US 11 67012703 67012703 single base substitution C T upstream_gene_variant UCEC-US 11 66888815 66888815 single base substitution T C exon_variant UCEC-US 11 66888815 66888815 single base substitution T C missense_variant Y10H 28T>C UCEC-US 11 66947569 66947569 single base substitution G A exon_variant UCEC-US 11 66947569 66947569 single base substitution G A missense_variant R21H 62G>A UCEC-US 11 66947577 66947577 single base substitution G T exon_variant UCEC-US 11 66947577 66947577 single base substitution G T missense_variant D24Y 70G>T UCEC-US 11 66975023 66975023 single base substitution A C missense_variant K117T 350A>C UCEC-US 11 66975023 66975023 single base substitution A C upstream_gene_variant UCEC-US 11 66983344 66983344 single base substitution T C downstream_gene_variant UCEC-US 11 66983344 66983344 single base substitution T C exon_variant UCEC-US 11 66983344 66983344 single base substitution T C missense_variant V204A 611T>C UCEC-US 11 66983344 66983344 single base substitution T C upstream_gene_variant UCEC-US 11 66985227 66985227 single base substitution C T downstream_gene_variant UCEC-US 11 66985227 66985227 single base substitution C T exon_variant UCEC-US 11 66985227 66985227 single base substitution C T missense_variant A238V 713C>T UCEC-US 11 66985227 66985227 single base substitution C T splice_region_variant UCEC-US 11 66995534 66995534 single base substitution C T exon_variant UCEC-US 11 66995534 66995534 single base substitution C T synonymous_variant F328F 984C>T UCEC-US 11 66995534 66995534 single base substitution C T upstream_gene_variant UCEC-US 11 66995540 66995540 single base substitution T C exon_variant UCEC-US 11 66995540 66995540 single base substitution T C synonymous_variant Y330Y 990T>C UCEC-US 11 66995540 66995540 single base substitution T C upstream_gene_variant UCEC-US 11 67010552 67010552 single base substitution A C 5_prime_UTR_variant UCEC-US 11 67010552 67010552 single base substitution A C exon_variant UCEC-US 11 67010552 67010552 single base substitution A C intron_variant UCEC-US 11 67010552 67010552 single base substitution A C missense_variant K518Q 1552A>C UCEC-US 11 67010552 67010552 single base substitution A C missense_variant K79Q 235A>C UCEC-US 11 67010552 67010552 single base substitution A C upstream_gene_variant UCEC-US 11 67012811 67012811 single base substitution G A downstream_gene_variant UCEC-US 11 67012811 67012811 single base substitution G A exon_variant UCEC-US 11 67012811 67012811 single base substitution G A missense_variant R133Q 398G>A UCEC-US 11 67012811 67012811 single base substitution G A missense_variant R30Q 89G>A UCEC-US 11 67012811 67012811 single base substitution G A missense_variant R572Q 1715G>A UCEC-US 11 67012811 67012811 single base substitution G A upstream_gene_variant UCEC-US 11 67012821 67012821 single base substitution A C downstream_gene_variant UCEC-US 11 67012821 67012821 single base substitution A C exon_variant UCEC-US 11 67012821 67012821 single base substitution A C missense_variant K136N 408A>C UCEC-US 11 67012821 67012821 single base substitution A C missense_variant K33N 99A>C UCEC-US 11 67012821 67012821 single base substitution A C missense_variant K575N 1725A>C UCEC-US 11 67012821 67012821 single base substitution A C upstream_gene_variant UCEC-US 11 67017605 67017605 single base substitution C A downstream_gene_variant UCEC-US 11 67017605 67017605 single base substitution C A exon_variant UCEC-US 11 67017605 67017605 single base substitution C A missense_variant L160M 478C>A UCEC-US 11 67017605 67017605 single base substitution C A missense_variant L263M 787C>A UCEC-US 11 67017605 67017605 single base substitution C A missense_variant L702M 2104C>A UCEC-US 11 67017605 67017605 single base substitution C A upstream_gene_variant UCEC-US 11 67017760 67017760 single base substitution C T downstream_gene_variant UCEC-US 11 67017760 67017760 single base substitution C T exon_variant UCEC-US 11 67017760 67017760 single base substitution C T synonymous_variant R211R 633C>T UCEC-US 11 67017760 67017760 single base substitution C T synonymous_variant R314R 942C>T UCEC-US 11 67017760 67017760 single base substitution C T synonymous_variant R753R 2259C>T UCEC-US 11 67017760 67017760 single base substitution C T upstream_gene_variant UCEC-US 11 67021049 67021049 single base substitution C T 3_prime_UTR_variant UCEC-US 11 67021049 67021049 single base substitution C T downstream_gene_variant UCEC-US 11 67021049 67021049 single base substitution C T exon_variant UCEC-US 11 67021049 67021049 single base substitution C T missense_variant R1020W 3058C>T UCEC-US 11 67021049 67021049 single base substitution C T missense_variant R478W 1432C>T UCEC-US 11 67021049 67021049 single base substitution C T missense_variant R581W 1741C>T UCEC-US 11 67022438 67022438 single base substitution G A 3_prime_UTR_variant UCEC-US 11 67022438 67022438 single base substitution G A exon_variant UCEC-US 11 67022438 67022438 single base substitution G A missense_variant R1134Q 3401G>A UCEC-US 11 67022438 67022438 single base substitution G A missense_variant R592Q 1775G>A UCEC-US 11 67022438 67022438 single base substitution G A missense_variant R695Q 2084G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-22-5482-01 COSM690379 c.2258G>A p.R753H Substitution - Missense 11:67250288-67250288 + ESO-805 COSM1255482 c.3136C>T p.L1046L Substitution - coding silent 11:67254247-67254247 + SW48 COSM2041353 c.1158C>T p.S386S Substitution - coding silent 11:67231639-67231639 + TCGA-HT-8564-01 COSM3967777 c.1696C>T p.R566W Substitution - Missense 11:67245321-67245321 + TCGA-AP-A059-01 COSM931016 c.990T>C p.Y330Y Substitution - coding silent 11:67228069-67228069 + BCM371T COSM4951669 c.2125G>T p.D709Y Substitution - Missense 11:67250155-67250155 + TCGA-AA-3492-01 COSM1356360 c.2495delC p.R834fs*3 Deletion - Frameshift 11:67250525-67250525 + TCGA-CJ-4895-01 COSM3359357 c.2208G>A p.V736V Substitution - coding silent 11:67250238-67250238 + DLD1 COSM2041354 c.1244C>T p.P415L Substitution - Missense 11:67231725-67231725 + TCGA-AX-A0J1-01 COSM931020 c.2104C>A p.L702M Substitution - Missense 11:67250134-67250134 + TCGA-G4-6320-01 COSM3687567 c.485C>T p.T162M Substitution - Missense 11:67207687-67207687 + TP_2020 COSM5567213 c.312T>G p.S104R Substitution - Missense 11:67207514-67207514 + SA090 COSM213566 c.1582C>T p.P528S Substitution - Missense 11:67245207-67245207 + HCT15 COSM2041370 c.1887T>C p.N629N Substitution - coding silent 11:67246038-67246038 + 5853_CLM COSM5753786 c.1900G>C p.D634H Substitution - Missense 11:67246051-67246051 + 2246952 COSM4413456 c.2651G>T p.W884L Substitution - Missense 11:67250681-67250681 + TCGA-D1-A167-01 COSM931021 c.2259C>T p.R753R Substitution - coding silent 11:67250289-67250289 + ESCC_BICR_064T COSM5437049 c.438C>T p.L146L Substitution - coding silent 11:67207640-67207640 + 1N46-VS-1T46 COSM4694876 c.3181C>T p.R1061C Substitution - Missense 11:67254292-67254292 + CHC892T COSM4796801 c.1564-1G>A p.? Unknown 11:67245188-67245188 + TCGA-EW-A1PB-01 COSM1475802 c.1307G>A p.G436E Substitution - Missense 11:67231788-67231788 + TCGA-B5-A0JY-01 COSM931018 c.1715G>A p.R572Q Substitution - Missense 11:67245340-67245340 + UPCI:SCC090 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + RMS106_ COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-D1-A16X-01 COSM931015 c.984C>T p.F328F Substitution - coding silent 11:67228063-67228063 + T578 COSM1356364 c.3133C>T p.R1045W Substitution - Missense 11:67254244-67254244 + UM-SCC-4 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + 3N52-VS-3T52 COSM4983396 c.1614G>A p.T538T Substitution - coding silent 11:67245239-67245239 + TCGA-CJ-6033-01 COSM467300 c.2405C>T p.T802M Substitution - Missense 11:67250435-67250435 + TCGA-Q1-A6DW-01 COSM4855895 c.3297C>A p.L1099L Substitution - coding silent 11:67254408-67254408 + TCGA-BH-A1ET-01 COSM429691 c.1480-1G>T p.? Unknown 11:67243008-67243008 + sysucc-880T COSM5462071 c.594-2A>G p.? Unknown 11:67215854-67215854 + UM-SCC-47 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + UM-SCC-17B COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-18-3414-01 COSM690383 c.662G>T p.W221L Substitution - Missense 11:67215924-67215924 + J90_T COSM3953703 c.1396G>A p.D466N Substitution - Missense 11:67231877-67231877 + 8051974 COSM3383761 c.307+1G>T p.? Unknown 11:67181893-67181893 + CAL33 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-BR-8591-01 COSM4035916 c.2667C>T p.D889D Substitution - coding silent 11:67250697-67250697 + RK048_C COSM1628186 c.1702C>T p.R568* Substitution - Nonsense 11:67245327-67245327 + ESOSCC156T COSM1171829 c.3423C>G p.I1141M Substitution - Missense 11:67254989-67254989 + T3535 COSM4694875 c.2501G>T p.R834L Substitution - Missense 11:67250531-67250531 + TCGA-HC-A4ZV-01 COSM3670872 c.2455C>A p.L819M Substitution - Missense 11:67250485-67250485 + TCGA-EE-A3JD-06 COSM4395199 c.2869C>T p.L957F Substitution - Missense 11:67252794-67252794 + SCC-9 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + HCC145T COSM5811451 c.49A>G p.T17A Substitution - Missense 11:67180085-67180085 + TCGA-24-0968-01 COSM77941 c.2879G>A p.S960N Substitution - Missense 11:67252804-67252804 + SNU-175 COSM2041411 c.2916C>T p.L972L Substitution - coding silent 11:67252841-67252841 + CSCC-27-T COSM4478196 c.2219C>T p.S740F Substitution - Missense 11:67250249-67250249 + TCGA-AA-3812-01 COSM270707 c.2379G>T p.K793N Substitution - Missense 11:67250409-67250409 + TCGA-E9-A5UO-01 COSM3810197 c.1603A>G p.I535V Substitution - Missense 11:67245228-67245228 + 104871 COSM94276 c.2501G>A p.R834H Substitution - Missense 11:67250531-67250531 + TCGA-AM-5821-01 COSM3687568 c.1079G>A p.S360N Substitution - Missense 11:67228158-67228158 + PT17_1 COSM5899033 c.242C>T p.S81F Substitution - Missense 11:67181380-67181380 + C0025T COSM4165922 c.594-5G>A p.? Unknown 11:67215851-67215851 + ESO-151 COSM1255481 c.438C>A p.L146L Substitution - coding silent 11:67207640-67207640 + RH18C COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + YUKAT COSM5373356 c.402G>A p.E134E Substitution - coding silent 11:67207604-67207604 + TCGA-CM-6162-01 COSM1356359 c.2198G>A p.R733Q Substitution - Missense 11:67250228-67250228 + BD14T COSM5517161 c.2933-10T>A p.? Unknown 11:67253443-67253443 + Pat_45_B COSM5839359 c.2967G>A p.W989* Substitution - Nonsense 11:67253487-67253487 + TCGA-EE-A3AF-06 COSM3452251 c.2819C>T p.A940V Substitution - Missense 11:67252744-67252744 + TCGA-BR-8487-01 COSM4035918 c.2707C>T p.R903C Substitution - Missense 11:67250737-67250737 + TCGA-E2-A1B0-01 COSM429692 c.2987G>A p.S996N Substitution - Missense 11:67253507-67253507 + 90482 COSM329439 c.2239G>A p.D747N Substitution - Missense 11:67250269-67250269 + TCGA-EE-A3JD-06 COSM4395807 c.1169C>T p.S390F Substitution - Missense 11:67231650-67231650 + RMS88_ COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-IM-A3U2-01 COSM3368524 c.1607C>T p.P536L Substitution - Missense 11:67245232-67245232 + HCC043T COSM5811971 c.1377A>C p.E459D Substitution - Missense 11:67231858-67231858 + 2521260 COSM5891440 c.190G>T p.V64L Substitution - Missense 11:67181328-67181328 + YUKAT COSM5373357 c.1371G>A p.E457E Substitution - coding silent 11:67231852-67231852 + TCGA-FW-A3R5-06 COSM3869979 c.3445C>T p.L1149F Substitution - Missense 11:67255011-67255011 + 5853_CLM COSM5753787 c.2035G>A p.D679N Substitution - Missense 11:67248350-67248350 + SNU-C2B COSM2041395 c.2500C>A p.R834S Substitution - Missense 11:67250530-67250530 + PCSI_0218_Pa_P_526 COSM3788037 c.1270G>T p.D424Y Substitution - Missense 11:67231751-67231751 + TCGA-AP-A056-01 COSM931019 c.1725A>C p.K575N Substitution - Missense 11:67245350-67245350 + CHC917T COSM3666979 c.686A>C p.K229T Substitution - Missense 11:67215948-67215948 + TCGA-70-6723-01 COSM690381 c.1016G>A p.R339H Substitution - Missense 11:67228095-67228095 + TCGA-BT-A20T-01 COSM415788 c.3058C>T p.R1020W Substitution - Missense 11:67253578-67253578 + HCT15 COSM2041354 c.1244C>T p.P415L Substitution - Missense 11:67231725-67231725 + HF-19967 COSM1192971 c.729delG p.Y244fs*50 Deletion - Frameshift 11:67217772-67217772 + T658 COSM4694873 c.1619C>T p.P540L Substitution - Missense 11:67245244-67245244 + TCGA-CF-A1HS-01 COSM415789 c.2320C>T p.R774W Substitution - Missense 11:67250350-67250350 + TCGA-A2-A1G4-01 COSM1475800 c.1063C>T p.Q355* Substitution - Nonsense 11:67228142-67228142 + TCGA-BR-4363-01 COSM4035922 c.3298A>G p.N1100D Substitution - Missense 11:67254409-67254409 + TCGA-EK-A2H0-01 COSM4819096 c.2238C>G p.S746R Substitution - Missense 11:67250268-67250268 + CHC892T COSM4796801 c.1564-1G>A p.? Unknown 11:67245188-67245188 + TCGA-EK-A3GM-01 COSM4823285 c.1155G>C p.L385F Substitution - Missense 11:67231636-67231636 + 61 COSM5739345 c.1865T>C p.L622P Substitution - Missense 11:67246016-67246016 + SNU-175 COSM2041366 c.1704A>G p.R568R Substitution - coding silent 11:67245329-67245329 + TCGA-A6-6780-01 COSM1356354 c.894delT p.L300fs*10 Deletion - Frameshift 11:67219340-67219340 + TCGA-FW-A3R5-06 COSM3869978 c.2390C>T p.S797L Substitution - Missense 11:67250420-67250420 + TCGA-BP-4352-01 COSM3359358 c.3216T>G p.S1072R Substitution - Missense 11:67254327-67254327 + RMS77_ COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-D1-A16G-01 COSM931014 c.713C>T p.A238V Substitution - Missense 11:67217756-67217756 + TCGA-AA-3672-01 COSM266751 c.410G>A p.R137Q Substitution - Missense 11:67207612-67207612 + STC291 COSM5051074 c.43C>T p.R15C Substitution - Missense 11:67180079-67180079 + TCGA-AP-A054-01 COSM931009 c.28T>C p.Y10H Substitution - Missense 11:67121344-67121344 + TCGA-BS-A0UV-01 COSM415788 c.3058C>T p.R1020W Substitution - Missense 11:67253578-67253578 + TCGA-DK-A2I4-01 COSM3791853 c.3052C>G p.Q1018E Substitution - Missense 11:67253572-67253572 + TCGA-E2-A2P6-01 COSM3810194 c.828C>T p.F276F Substitution - coding silent 11:67217871-67217871 + Pat_14_B COSM5839357 c.640G>A p.D214N Substitution - Missense 11:67215902-67215902 + C91 COSM1628186 c.1702C>T p.R568* Substitution - Nonsense 11:67245327-67245327 + TCGA-EK-A3GM-01 COSM4823312 c.1065G>C p.Q355H Substitution - Missense 11:67228144-67228144 + TCGA-EE-A2MR-06 COSM3452250 c.1714C>T p.R572* Substitution - Nonsense 11:67245339-67245339 + TCGA-G3-A25S-01 COSM4926981 c.1376A>G p.E459G Substitution - Missense 11:67231857-67231857 + TCGA-AC-A23H-01 COSM3810195 c.1318G>A p.D440N Substitution - Missense 11:67231799-67231799 + T2269 COSM4694872 c.1384C>T p.R462C Substitution - Missense 11:67231865-67231865 + TCGA-D7-8575-01 COSM4035920 c.3047A>G p.D1016G Substitution - Missense 11:67253567-67253567 + BCM371T COSM4951669 c.2125G>T p.D709Y Substitution - Missense 11:67250155-67250155 + CSCC-41-T COSM4508820 c.788C>G p.S263* Substitution - Nonsense 11:67217831-67217831 + TCGA-EK-A3GK-01 COSM4854509 c.3477G>A p.Q1159Q Substitution - coding silent 11:67255043-67255043 + TCGA-BR-6452-01 COSM4035915 c.2388A>T p.G796G Substitution - coding silent 11:67250418-67250418 + SNU-175 COSM2041368 c.1782T>C p.F594F Substitution - coding silent 11:67245407-67245407 + TCGA-13-0760-01 COSM75102 c.3349C>T p.R1117C Substitution - Missense 11:67254915-67254915 + PD13307a COSM1171829 c.3423C>G p.I1141M Substitution - Missense 11:67254989-67254989 + TCGA-13-0889-01 COSM77940 c.667C>T p.H223Y Substitution - Missense 11:67215929-67215929 + PCSI_0210_Pa_P_526 COSM3810194 c.828C>T p.F276F Substitution - coding silent 11:67217871-67217871 + WSU-HN30 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + RMS80_ COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-B0-5098-01 COSM1492690 c.1469C>T p.A490V Substitution - Missense 11:67231950-67231950 + TCGA-AN-A046-01 COSM3810193 c.59G>A p.R20Q Substitution - Missense 11:67180095-67180095 + LIM2405 COSM4613273 c.2616delG p.G874fs*5 Deletion - Frameshift 11:67250646-67250646 + TCGA-EE-A29V-06 COSM3452249 c.1674C>T p.S558S Substitution - coding silent 11:67245299-67245299 + TCGA-EK-A2RA-01 COSM4848397 c.474G>A p.Q158Q Substitution - coding silent 11:67207676-67207676 + BD212T COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-BS-A0UV-01 COSM931022 c.3401G>A p.R1134Q Substitution - Missense 11:67254967-67254967 + Pat_70_B COSM2041403 c.2578_2580delGAG p.E866delE Deletion - In frame 11:67250608-67250610 + UM-SCC-11B COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + ccRCC-49 COSM931022 c.3401G>A p.R1134Q Substitution - Missense 11:67254967-67254967 + TCGA-EA-A5O9-01 COSM4851897 c.3203G>A p.R1068Q Substitution - Missense 11:67254314-67254314 + MZ7-mel COSM25630 c.3014C>T p.T1005I Substitution - Missense 11:67253534-67253534 + 2246945 COSM4413455 c.1822C>T p.Q608* Substitution - Nonsense 11:67245447-67245447 + sysucc-274T COSM5475562 c.1681G>A p.V561M Substitution - Missense 11:67245306-67245306 + OSCC-GB_01120111 COSM4884759 c.2631G>T p.R877S Substitution - Missense 11:67250661-67250661 + 91112 COSM329440 c.2124C>T p.C708C Substitution - coding silent 11:67250154-67250154 + TCGA-61-1915-01 COSM1322224 c.3208G>A p.D1070N Substitution - Missense 11:67254319-67254319 + KYSE-150 COSM2041419 c.3192C>G p.P1064P Substitution - coding silent 11:67254303-67254303 + WSU-HN8 COSM4602837 c.3487T>G p.*1163E Nonstop extension 11:67255053-67255053 + TCGA-AA-3713-01 COSM1356361 c.2559delG p.G855fs*24 Deletion - Frameshift 11:67250589-67250589 + STC232 COSM5051076 c.1971C>T p.D657D Substitution - coding silent 11:67248286-67248286 + TCGA-A8-A0A6-01 COSM3810196 c.1576A>C p.T526P Substitution - Missense 11:67245201-67245201 + SJHYPO052 COSM4775899 c.72T>C p.D24D Substitution - coding silent 11:67180108-67180108 + CSCC-31-T COSM4506490 c.721C>T p.L241L Substitution - coding silent 11:67217764-67217764 + TCGA-AP-A059-01 COSM931011 c.70G>T p.D24Y Substitution - Missense 11:67180106-67180106 + ESCC-214T COSM3935597 c.3420C>T p.F1140F Substitution - coding silent 11:67254986-67254986 + TCGA-E9-A1NA-01 COSM5831837 c.2531delC p.Q846fs*33 Deletion - Frameshift 11:67250561-67250561 + N-Thy017 COSM5095369 c.3225C>A p.S1075R Substitution - Missense 11:67254336-67254336 + RH30SJ_ COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + YUKAT COSM5373358 c.2166G>A p.M722I Substitution - Missense 11:67250196-67250196 + 93VU147T COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + Pat_59_A COSM5839358 c.1267G>A p.G423R Substitution - Missense 11:67231748-67231748 + TCGA-BR-8382-01 COSM2041402 c.2577A>G p.E859E Substitution - coding silent 11:67250607-67250607 + CAL27 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + T578 COSM4694871 c.158T>G p.F53C Substitution - Missense 11:67180194-67180194 + TCGA-D1-A17Q-01 COSM931017 c.1552A>C p.K518Q Substitution - Missense 11:67243081-67243081 + C0088T COSM4165923 c.644T>C p.F215S Substitution - Missense 11:67215906-67215906 + T3080 COSM4694876 c.3181C>T p.R1061C Substitution - Missense 11:67254292-67254292 + 113368 COSM94275 c.2334C>A p.N778K Substitution - Missense 11:67250364-67250364 + TCGA-HU-A4H4-01 COSM4035917 c.2681A>G p.Q894R Substitution - Missense 11:67250711-67250711 + SJHGG045_A COSM4970858 c.2386G>A p.G796R Substitution - Missense 11:67250416-67250416 + CHC917T COSM3666979 c.686A>C p.K229T Substitution - Missense 11:67215948-67215948 + TCGA-DD-A1EB-01 COSM4928639 c.444T>A p.F148L Substitution - Missense 11:67207646-67207646 + TCGA-AN-A0AK-01 COSM1356360 c.2495delC p.R834fs*3 Deletion - Frameshift 11:67250525-67250525 + ATL044 COSM5704150 c.496A>G p.I166V Substitution - Missense 11:67215349-67215349 + PT46 COSM2041380 c.2192C>T p.S731F Substitution - Missense 11:67250222-67250222 + PD4203a COSM161880 c.2781G>A p.K927K Substitution - coding silent 11:67252706-67252706 + 15 COSM5733012 c.3443_3444insGCCTCTACT p.S1148>RPLL Complex - insertion inframe 11:67255009-67255010 + 86567 COSM95880 c.3009C>G p.L1003L Substitution - coding silent 11:67253529-67253529 + ORL-48 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + CT-TC COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + GHE0776 COSM5714759 c.3217C>T p.H1073Y Substitution - Missense 11:67254328-67254328 + HCC071T COSM5821644 c.1057G>T p.E353* Substitution - Nonsense 11:67228136-67228136 + LUAD-VUMN6 COSM347808 c.2715C>G p.L905L Substitution - coding silent 11:67250745-67250745 + SNU-175 COSM2041346 c.800G>A p.R267H Substitution - Missense 11:67217843-67217843 + TCGA-EE-A3JI-06 COSM3452248 c.1109C>T p.S370F Substitution - Missense 11:67231590-67231590 + HCC2998 COSM415788 c.3058C>T p.R1020W Substitution - Missense 11:67253578-67253578 + DLD1 COSM2041370 c.1887T>C p.N629N Substitution - coding silent 11:67246038-67246038 + TCGA-BD-A3EP-01 COSM4911605 c.571A>T p.M191L Substitution - Missense 11:67215424-67215424 + AA1934 COSM4168379 c.2578_2579insGGG p.E859_E860insG Insertion - In frame 11:67250608-67250609 + PTC-14C COSM4146183 c.599G>C p.C200S Substitution - Missense 11:67215861-67215861 + TCGA-A6-6781-01 COSM1356364 c.3133C>T p.R1045W Substitution - Missense 11:67254244-67254244 + SCC-25 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + NOKSI COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + KM12 COSM1356361 c.2559delG p.G855fs*24 Deletion - Frameshift 11:67250589-67250589 + SCC-15 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + CRC-20T COSM5482413 c.2280G>T p.R760R Substitution - coding silent 11:67250310-67250310 + ESO-859 COSM1239207 c.267G>A p.P89P Substitution - coding silent 11:67181852-67181852 + pfg160T COSM4756781 c.2528G>A p.R843Q Substitution - Missense 11:67250558-67250558 + C0076T COSM4165924 c.2002A>C p.N668H Substitution - Missense 11:67248317-67248317 + CSCC-44-T COSM4565873 c.2642_2643GG>AA p.R881Q Substitution - Missense 11:67250672-67250673 + HCC62T COSM1605105 c.2416C>T p.P806S Substitution - Missense 11:67250446-67250446 + HCC62 COSM1605105 c.2416C>T p.P806S Substitution - Missense 11:67250446-67250446 + TCGA-BR-8368-01 COSM4035912 c.1300C>T p.H434Y Substitution - Missense 11:67231781-67231781 + TCGA-HC-8216-01 COSM3670871 c.1409C>A p.S470Y Substitution - Missense 11:67231890-67231890 + TCGA-D1-A17Q-01 COSM931012 c.350A>C p.K117T Substitution - Missense 11:67207552-67207552 + YUROG COSM5373359 c.2495C>T p.S832F Substitution - Missense 11:67250525-67250525 + ESCC_16 COSM429693 c.3307+2T>G p.? Unknown 11:67254420-67254420 + sysucc-912T COSM5764947 c.1993G>T p.E665* Substitution - Nonsense 11:67248308-67248308 + BICR_22 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-BR-4362-01 COSM4035913 c.1480A>G p.I494V Substitution - Missense 11:67243009-67243009 + S02139 COSM5674055 c.59G>T p.R20L Substitution - Missense 11:67180095-67180095 + PT37 COSM5920138 c.2488C>T p.R830C Substitution - Missense 11:67250518-67250518 + TCGA-F4-6856-01 COSM1356357 c.1905T>C p.F635F Substitution - coding silent 11:67246056-67246056 + STC252 COSM5051075 c.1303A>G p.N435D Substitution - Missense 11:67231784-67231784 + TCGA-66-2734-01 COSM690384 c.46G>T p.G16C Substitution - Missense 11:67180082-67180082 + TCGA-AD-6964-01 COSM3687789 c.2462C>T p.A821V Substitution - Missense 11:67250492-67250492 + WSU-HN12 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-24-1417-01 COSM117772 c.2380A>C p.I794L Substitution - Missense 11:67250410-67250410 + TCGA-CG-5733-01 COSM4035919 c.2981C>T p.A994V Substitution - Missense 11:67253501-67253501 + GB07 COSM1743611 c.1144C>G p.P382A Substitution - Missense 11:67231625-67231625 + WSU-HN13 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + RK262_C01 COSM4778743 c.2570A>T p.E857V Substitution - Missense 11:67250600-67250600 + S01516 COSM5668989 c.3278G>C p.R1093P Substitution - Missense 11:67254389-67254389 + TCGA-G2-A2EO-01 COSM1298488 c.3369G>A p.L1123L Substitution - coding silent 11:67254935-67254935 + YUPAER COSM5373360 c.2951T>A p.L984Q Substitution - Missense 11:67253471-67253471 + SMS-CTR COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + WSU-HN8 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + STC252 COSM5051077 c.2683C>T p.R895W Substitution - Missense 11:67250713-67250713 + TCGA-AA-3831-01 COSM295027 c.2422A>G p.K808E Substitution - Missense 11:67250452-67250452 + TCGA-G3-A25W-01 COSM1255481 c.438C>A p.L146L Substitution - coding silent 11:67207640-67207640 + TCGA-EK-A2PL-01 COSM4838290 c.373C>T p.Q125* Substitution - Nonsense 11:67207575-67207575 + ESCC_29 COSM5627435 c.10G>A p.E4K Substitution - Missense 11:67121326-67121326 + CSCC-10-T COSM4511002 c.854C>T p.A285V Substitution - Missense 11:67219300-67219300 + BHY COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + UM-SCC-2 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + ESCC_62 COSM5633011 c.3401G>C p.R1134P Substitution - Missense 11:67254967-67254967 + 107529 COSM95881 c.3126C>G p.T1042T Substitution - coding silent 11:67254237-67254237 + T2269 COSM4694874 c.2287C>T p.L763L Substitution - coding silent 11:67250317-67250317 + TCGA-CA-6717-01 COSM1356352 c.443T>G p.F148C Substitution - Missense 11:67207645-67207645 + 01-P8014 COSM2041333 c.324G>A p.V108V Substitution - coding silent 11:67207526-67207526 + DN14042 COSM5962502 c.1669G>A p.A557T Substitution - Missense 11:67245294-67245294 + SNUH_G15_S1 COSM3676281 c.2130G>C p.E710D Substitution - Missense 11:67250160-67250160 + WSU-HN6 COSM4590278 c.310A>G p.S104G Substitution - Missense 11:67207512-67207512 + TCGA-DD-A1EB-01 COSM4928810 c.938A>G p.N313S Substitution - Missense 11:67219384-67219384 + LIM1899 COSM4639778 c.1926C>T p.C642C Substitution - coding silent 11:67246077-67246077 + Au4 COSM5603863 c.2339C>T p.P780L Substitution - Missense 11:67250369-67250369 + T1204 COSM4694877 c.3202C>T p.R1068* Substitution - Nonsense 11:67254313-67254313 + 112509 COSM94274 c.2206G>C p.V736L Substitution - Missense 11:67250236-67250236 + Pat_32_B COSM2041403 c.2578_2580delGAG p.E866delE Deletion - In frame 11:67250608-67250610 + RK048_C01 COSM1628186 c.1702C>T p.R568* Substitution - Nonsense 11:67245327-67245327 + L03 COSM5368588 c.1021G>C p.V341L Substitution - Missense 11:67228100-67228100 + TCGA-CD-A4MI-01 COSM4035921 c.3293A>G p.E1098G Substitution - Missense 11:67254404-67254404 + UM-SCC-11B COSM4598052 c.1282G>A p.D428N Substitution - Missense 11:67231763-67231763 + TCGA-BR-8487-01 COSM4035923 c.3352A>G p.I1118V Substitution - Missense 11:67254918-67254918 + TCGA-AP-A051-01 COSM931010 c.62G>A p.R21H Substitution - Missense 11:67180098-67180098 + 8069329 COSM3769421 c.2365G>T p.V789F Substitution - Missense 11:67250395-67250395 + TCGA-B5-A11E-01 COSM931013 c.611T>C p.V204A Substitution - Missense 11:67215873-67215873 + TCGA-BR-4361-01 COSM4035914 c.2250T>C p.S750S Substitution - coding silent 11:67250280-67250280 + TCGA-D1-A103-01 COSM415788 c.3058C>T p.R1020W Substitution - Missense 11:67253578-67253578 + SJDES006 COSM4574708 c.3021_3025delTCTTC p.D1007fs*20 Deletion - Frameshift 11:67253541-67253545 + TCGA-GN-A266-06 COSM3452247 c.215T>A p.L72* Substitution - Nonsense 11:67181353-67181353 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.124147 11q13.2 605657 2467135|CGAP|BC047371|C/T|non-coding||3444|Candidate; 2467135|CGAP|BC047486|C/T|non-coding||4282|Candidate; 2467135|CGAP|BC064360|C/T|non-coding||4147|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.E58D c.174A>C 11 66947681 LUAD A C Missense p.I794L c.2380A>C 11 67017881 OV A G IntronicSNV . c.1480-2761A>G 11 67007719 HC A G Missense p.K808E c.2422A>G 11 67017923 COREAD A T Synonymous p.S617S c.1851A>T 11 67013473 LUAD C A Missense p.L819M c.2455C>A 11 67017956 PRAD C A Missense p.S470Y c.1409C>A 11 66999361 PRAD C A Synonymous p.R1068R c.3202C>A 11 67021784 LUAD C A Synonymous p.R446R c.1336C>A 11 66999288 STAD C - Frameshift p.H349Tfs*2 c.1045delC 11 66995593 THCA C G IntronicSNV . c.957+25C>G 11 66986899 CM C G Missense p.Q1018E c.3052C>G 11 67021043 BLCA C G Missense p.S1095C c.3284C>G 11 67021866 LUAD C T IntronicSNV . c.1833+214C>T 11 67013143 CM C T Missense p.A238V c.713C>T 11 66985227 UCEC C T Missense p.A940V c.2819C>T 11 67020215 CM C T Missense p.H223Y c.667C>T 11 66983400 OV C T Missense p.L957F c.2869C>T 11 67020265 CM C T Missense p.P528S c.1582C>T 11 67012678 BRCA C T Missense p.P536L c.1607C>T 11 67012703 THCA C T Missense p.P673S c.2017C>T 11 67015803 CM C T Missense p.R1020W c.3058C>T 11 67021049 BLCA C T Missense p.R1117C c.3349C>T 11 67022386 OV C T Missense p.R774W c.2320C>T 11 67017821 BLCA C T Missense p.R9C c.25C>T 11 66888812 HNSC C T Missense p.S370F c.1109C>T 11 66999061 CM C T Missense p.S390F c.1169C>T 11 66999121 CM C T Missense p.T802M c.2405C>T 11 67017906 RCCC C T Nonsense p.Q355* c.1063C>T 11 66995613 BRCA C T Nonsense p.R568* c.1702C>T 11 67012798 HC C T Synonymous p.L1046L c.3136C>T 11 67021718 ESCA C T Synonymous p.P235P c.705C>T 11 66985219 HNSC C T Synonymous p.S558S c.1674C>T 11 67012770 CM C T Synonymous p.Y798Y c.2394C>T 11 67017895 CM G A Missense p.E376K c.1126G>A 11 66999078 BRCA G A Missense p.G436E c.1307G>A 11 66999259 BRCA G A Missense p.R1035H c.3104G>A 11 67021686 STAD G A Missense p.R339H c.1016G>A 11 66995566 LUSC G A Missense p.R753H c.2258G>A 11 67017759 LUSC G A Missense p.S960N c.2879G>A 11 67020275 OV G A Missense p.S996N c.2987G>A 11 67020978 BRCA G A Synonymous p.E860E c.2580G>A 11 67018081 THCA G A Synonymous p.K927K c.2781G>A 11 67020177 BRCA G A Synonymous p.L1123L c.3369G>A 11 67022406 BLCA G A Synonymous p.P89P c.267G>A 11 66949323 ESCA G A Synonymous p.V736V c.2208G>A 11 67017709 RCCC G T Missense p.G16C c.46G>T 11 66947553 LUSC G T Missense p.K793N c.2379G>T 11 67017880 COREAD G T Missense p.R703L c.2108G>T 11 67017609 STAD G T Missense p.W221L c.662G>T 11 66983395 LUSC G T SpliceAcceptorSNV . c.1480-1G>T 11 67010479 BRCA T C Missense p.Y10H c.28T>C 11 66888815 UCEC T G Missense p.S1072R c.3216T>G 11 67021798 RCCC T - IntronicDeletion . c.1-393delT 11 66888385 CM