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 ACC 11 62376216 62376216 + Missense_Mutation SNP C C T TCGA-OR-A5J4-01A-11D-A29I-10 TCGA-OR-A5J4-10A-01D-A29L-10 g.chr11:62376216C>T c.991G>A c.(991-993)Gat>Aat p.D331N ACC 11 62378802 62378802 + Missense_Mutation SNP G G C TCGA-OR-A5KX-01A-11D-A29I-10 TCGA-OR-A5KX-10A-01D-A29L-10 g.chr11:62378802G>C c.209C>G c.(208-210)cCa>cGa p.P70R BLCA 11 62370239 62370239 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr11:62370239G>C c.2479C>G c.(2479-2481)Cgt>Ggt p.R827G BLCA 11 62372641 62372641 + Silent SNP G G C TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr11:62372641G>C c.1926C>G c.(1924-1926)ctC>ctG p.L642L BLCA 11 62376050 62376050 + Silent SNP G G A TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr11:62376050G>A c.1074C>T c.(1072-1074)ttC>ttT p.F358F BLCA 11 62376855 62376855 + Silent SNP T T C TCGA-E7-A97P-01A-11D-A38G-08 TCGA-E7-A97P-10A-01D-A38J-08 g.chr11:62376855T>C c.729A>G c.(727-729)ccA>ccG p.P243P BLCA 11 62378418 62378418 + Missense_Mutation SNP G G A TCGA-DK-A3IT-01A-31D-A20D-08 TCGA-DK-A3IT-10A-01D-A20D-08 g.chr11:62378418G>A c.499C>T c.(499-501)Cgg>Tgg p.R167W BLCA 11 62378910 62378910 + Missense_Mutation SNP G G A TCGA-FD-A3SO-01A-11D-A22Z-08 TCGA-FD-A3SO-10A-01D-A22Z-08 g.chr11:62378910G>A c.181C>T c.(181-183)Cct>Tct p.P61S BRCA 11 62370688 62370688 + Missense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:62370688C>A c.2289G>T c.(2287-2289)aaG>aaT p.K763N BRCA 11 62371661 62371661 + Silent SNP C C T TCGA-A2-A04V-01A-21W-A050-09 TCGA-A2-A04V-10A-01W-A055-09 g.chr11:62371661C>T c.1995G>A c.(1993-1995)ttG>ttA p.L665L BRCA 11 62376502 62376502 + Silent SNP T T C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:62376502T>C c.861A>G c.(859-861)ggA>ggG p.G287G BRCA 11 62378355 62378355 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:62378355C>T c.562G>A c.(562-564)Gag>Aag p.E188K BRCA 11 62378386 62378386 + Silent SNP G G A TCGA-BH-A1FL-01A-11D-A13L-09 TCGA-BH-A1FL-11A-13D-A13O-09 g.chr11:62378386G>A c.531C>T c.(529-531)tcC>tcT p.S177S BRCA 11 62378801 62378802 + Frame_Shift_Ins INS - - G TCGA-A2-A0CU-01A-12W-A050-09 TCGA-A2-A0CU-10A-01W-A055-09 g.chr11:62378801_62378802insG c.209_210insC c.(208-210)ccafs p.P70fs CESC 11 62370341 62370341 + Missense_Mutation SNP C C T TCGA-C5-A1MK-01A-11D-A14W-08 TCGA-C5-A1MK-10A-01D-A14W-08 g.chr11:62370341C>T c.2377G>A c.(2377-2379)Gat>Aat p.D793N CESC 11 62371633 62371633 + Missense_Mutation SNP C C T TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr11:62371633C>T c.2023G>A c.(2023-2025)Gat>Aat p.D675N CESC 11 62373588 62373588 + Missense_Mutation SNP C C G TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr11:62373588C>G c.1603G>C c.(1603-1605)Gac>Cac p.D535H CESC 11 62376235 62376235 + Missense_Mutation SNP C C G TCGA-R2-A69V-01A-11D-A32I-09 TCGA-R2-A69V-10A-01D-A32I-09 g.chr11:62376235C>G c.972G>C c.(970-972)caG>caC p.Q324H CHOL 11 62378802 62378802 + Missense_Mutation SNP G G T TCGA-W5-AA2T-01A-12D-A417-09 TCGA-W5-AA2T-10A-01D-A41A-09 g.chr11:62378802G>T c.209C>A c.(208-210)cCa>cAa p.P70Q COAD 11 62371639 62371639 + Missense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:62371639C>T c.2017G>A c.(2017-2019)Gtg>Atg p.V673M COAD 11 62372618 62372618 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:62372618C>A c.1949G>T c.(1948-1950)gGg>gTg p.G650V COAD 11 62374523 62374523 + Missense_Mutation SNP C C T TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr11:62374523C>T c.1411G>A c.(1411-1413)Gga>Aga p.G471R COAD 11 62376450 62376450 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:62376450T>C c.913A>G c.(913-915)Aca>Gca p.T305A COAD 11 62376886 62376886 + Missense_Mutation SNP A A G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr11:62376886A>G c.698T>C c.(697-699)aTc>aCc p.I233T COAD 11 62378459 62378459 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:62378459C>T c.458G>A c.(457-459)cGa>cAa p.R153Q COAD 11 62378798 62378799 + Frame_Shift_Ins INS - - C TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr11:62378798_62378799insC c.212_213insG c.(211-213)ggafs p.G71fs COAD 11 62378802 62378802 + Frame_Shift_Del DEL G G - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:62378802delG c.209delC c.(208-210)ccafs p.P70fs COAD 11 62378942 62378942 + Frame_Shift_Del DEL G G - TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:62378942delG c.149delC c.(148-150)cctfs p.P50fs COADREAD 11 62371639 62371639 + Missense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:62371639C>T c.2017G>A c.(2017-2019)Gtg>Atg p.V673M COADREAD 11 62372618 62372618 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:62372618C>A c.1949G>T c.(1948-1950)gGg>gTg p.G650V COADREAD 11 62374523 62374523 + Missense_Mutation SNP C C T TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr11:62374523C>T c.1411G>A c.(1411-1413)Gga>Aga p.G471R COADREAD 11 62376450 62376450 + Missense_Mutation SNP T T C TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr11:62376450T>C c.913A>G c.(913-915)Aca>Gca p.T305A COADREAD 11 62376886 62376886 + Missense_Mutation SNP A A G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr11:62376886A>G c.698T>C c.(697-699)aTc>aCc p.I233T COADREAD 11 62378459 62378459 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:62378459C>T c.458G>A c.(457-459)cGa>cAa p.R153Q COADREAD 11 62378798 62378799 + Frame_Shift_Ins INS - - C TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr11:62378798_62378799insC c.212_213insG c.(211-213)ggafs p.G71fs COADREAD 11 62378802 62378802 + Frame_Shift_Del DEL G G - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:62378802delG c.209delC c.(208-210)ccafs p.P70fs COADREAD 11 62378942 62378942 + Frame_Shift_Del DEL G G - TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr11:62378942delG c.149delC c.(148-150)cctfs p.P50fs ESCA 11 62371469 62371469 + Missense_Mutation SNP T T C TCGA-V5-A7RC-01B-11D-A403-09 TCGA-V5-A7RC-10A-01D-A403-09 g.chr11:62371469T>C c.2116A>G c.(2116-2118)Atc>Gtc p.I706V ESCA 11 62372637 62372638 + Frame_Shift_Del DEL CA CA - TCGA-LN-A4A4-01A-11D-A27G-09 TCGA-LN-A4A4-10A-01D-A27G-09 g.chr11:62372637_62372638delCA c.1929_1930delTG c.(1927-1932)tgtgctfs p.A644fs ESCA 11 62379057 62379057 + Missense_Mutation SNP C C T TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr11:62379057C>T c.34G>A c.(34-36)Gct>Act p.A12T GBM 11 62378668 62378668 + Nonsense_Mutation SNP C C A TCGA-32-2491-01A-01D-1353-08 TCGA-32-2491-10A-01D-1353-08 g.chr11:62378668C>A c.343G>T c.(343-345)Gag>Tag p.E115* GBMLGG 11 62374475 62374475 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:62374475G>A c.1459C>T c.(1459-1461)Cgg>Tgg p.R487W GBMLGG 11 62378668 62378668 + Nonsense_Mutation SNP C C A TCGA-32-2491-01A-01D-1353-08 TCGA-32-2491-10A-01D-1353-08 g.chr11:62378668C>A c.343G>T c.(343-345)Gag>Tag p.E115* HNSC 11 62373366 62373366 + Silent SNP C C G TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr11:62373366C>G c.1743G>C c.(1741-1743)ctG>ctC p.L581L HNSC 11 62373658 62373658 + Silent SNP G G A TCGA-QK-A6V9-01A-11D-A34J-08 TCGA-QK-A6V9-10B-01D-A34M-08 g.chr11:62373658G>A c.1533C>T c.(1531-1533)caC>caT p.H511H HNSC 11 62374473 62374473 + Silent SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr11:62374473C>T c.1461G>A c.(1459-1461)cgG>cgA p.R487R HNSC 11 62374514 62374514 + Missense_Mutation SNP G G C TCGA-HD-8635-01A-11D-2394-08 TCGA-HD-8635-10A-01D-2394-08 g.chr11:62374514G>C c.1420C>G c.(1420-1422)Ctc>Gtc p.L474V HNSC 11 62376848 62376848 + Nonsense_Mutation SNP C C A TCGA-QK-A8Z7-01A-11D-A391-08 TCGA-QK-A8Z7-10A-01D-A394-08 g.chr11:62376848C>A c.736G>T c.(736-738)Gag>Tag p.E246* HNSC 11 62376895 62376895 + Missense_Mutation SNP G G A TCGA-F7-A50J-01A-21D-A28R-08 TCGA-F7-A50J-10A-01D-A28U-08 g.chr11:62376895G>A c.689C>T c.(688-690)cCg>cTg p.P230L HNSC 11 62377166 62377166 + Missense_Mutation SNP C C T TCGA-T2-A6WX-01A-12D-A34J-08 TCGA-T2-A6WX-10B-01D-A34M-08 g.chr11:62377166C>T c.569G>A c.(568-570)cGt>cAt p.R190H KICH 11 62378660 62378660 + Silent SNP G G A TCGA-KN-8422-01A-11D-2310-10 TCGA-KN-8422-11A-01D-2310-10 g.chr11:62378660G>A c.351C>T c.(349-351)agC>agT p.S117S KIPAN 11 62376458 62376458 + Missense_Mutation SNP C C A TCGA-BQ-7046-01A-11D-1961-08 TCGA-BQ-7046-11A-01D-1961-08 g.chr11:62376458C>A c.905G>T c.(904-906)cGg>cTg p.R302L KIPAN 11 62378660 62378660 + Silent SNP G G A TCGA-KN-8422-01A-11D-2310-10 TCGA-KN-8422-11A-01D-2310-10 g.chr11:62378660G>A c.351C>T c.(349-351)agC>agT p.S117S KIRP 11 62376458 62376458 + Missense_Mutation SNP C C A TCGA-BQ-7046-01A-11D-1961-08 TCGA-BQ-7046-11A-01D-1961-08 g.chr11:62376458C>A c.905G>T c.(904-906)cGg>cTg p.R302L LGG 11 62374475 62374475 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:62374475G>A c.1459C>T c.(1459-1461)Cgg>Tgg p.R487W LIHC 11 62370651 62370651 + Missense_Mutation SNP A A G TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr11:62370651A>G c.2326T>C c.(2326-2328)Tac>Cac p.Y776H LIHC 11 62370679 62370679 + Silent SNP A A G TCGA-G3-A3CG-01A-11D-A20W-10 TCGA-G3-A3CG-10A-01D-A20W-10 g.chr11:62370679A>G c.2298T>C c.(2296-2298)taT>taC p.Y766Y LIHC 11 62370721 62370721 + Splice_Site SNP T T G TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr11:62370721T>G c.e20-2 LIHC 11 62373664 62373664 + Silent SNP C C T TCGA-DD-A73D-01A-12D-A32G-10 TCGA-DD-A73D-10A-01D-A32G-10 g.chr11:62373664C>T c.1527G>A c.(1525-1527)caG>caA p.Q509Q LIHC 11 62375157 62375157 + Missense_Mutation SNP C C A TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr11:62375157C>A c.1343G>T c.(1342-1344)cGg>cTg p.R448L LIHC 11 62375693 62375693 + Missense_Mutation SNP T T C TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr11:62375693T>C c.1186A>G c.(1186-1188)Atg>Gtg p.M396V LIHC 11 62379012 62379012 + Frame_Shift_Del DEL C C - TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr11:62379012delC c.79delG c.(79-81)gagfs p.E27fs LUAD 11 62371621 62371621 + Missense_Mutation SNP C C T TCGA-44-7660-01A-11D-2063-08 TCGA-44-7660-10A-01D-2063-08 g.chr11:62371621C>T c.2035G>A c.(2035-2037)Ggc>Agc p.G679S LUAD 11 62373360 62373360 + Silent SNP T T C TCGA-49-4494-01A-01D-1265-08 TCGA-49-4494-11A-01D-1265-08 g.chr11:62373360T>C c.1749A>G c.(1747-1749)ggA>ggG p.G583G LUAD 11 62375672 62375672 + Splice_Site SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr11:62375672C>A c.e10+1 LUAD 11 62375729 62375729 + Missense_Mutation SNP C C T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr11:62375729C>T c.1150G>A c.(1150-1152)Gag>Aag p.E384K LUAD 11 62377136 62377136 + Missense_Mutation SNP C C A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr11:62377136C>A c.599G>T c.(598-600)gGg>gTg p.G200V LUAD 11 62378649 62378649 + Missense_Mutation SNP G G A TCGA-55-A4DF-01A-11D-A24D-08 TCGA-55-A4DF-10A-01D-A24F-08 g.chr11:62378649G>A c.362C>T c.(361-363)tCt>tTt p.S121F LUAD 11 62378705 62378705 + Silent SNP C C T TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr11:62378705C>T c.306G>A c.(304-306)ctG>ctA p.L102L LUSC 11 62371615 62371615 + Missense_Mutation SNP C C G TCGA-66-2793-01A-01D-1267-08 TCGA-66-2793-11A-01D-1267-08 g.chr11:62371615C>G c.2041G>C c.(2041-2043)Gag>Cag p.E681Q LUSC 11 62373335 62373335 + Missense_Mutation SNP C C T TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr11:62373335C>T c.1774G>A c.(1774-1776)Gta>Ata p.V592I LUSC 11 62376917 62376917 + Missense_Mutation SNP G G A TCGA-70-6722-01A-11D-1817-08 TCGA-70-6722-10A-01D-1817-08 g.chr11:62376917G>A c.667C>T c.(667-669)Cgc>Tgc p.R223C LUSC 11 62378413 62378413 + Silent SNP C C T TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr11:62378413C>T c.504G>A c.(502-504)caG>caA p.Q168Q OV 11 62374563 62374563 + Missense_Mutation SNP C C G TCGA-36-2534-01A-01D-1526-09 TCGA-36-2534-10A-01D-1526-09 g.chr11:62374563C>G c.1371G>C c.(1369-1371)aaG>aaC p.K457N OV 11 62378798 62378799 + Frame_Shift_Ins INS - - C TCGA-24-1849-01A-01W-0639-09 TCGA-24-1849-10A-01W-0639-09 g.chr11:62378798_62378799insC c.212_213insG c.(211-213)ggafs p.G71fs PAAD 11 62370095 62370095 + Missense_Mutation SNP G G A TCGA-IB-A7LX-01A-12D-A36O-08 TCGA-IB-A7LX-10A-01D-A367-08 g.chr11:62370095G>A c.2543C>T c.(2542-2544)aCg>aTg p.T848M PAAD 11 62373565 62373565 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:62373565C>T c.1626G>A c.(1624-1626)ggG>ggA p.G542G PAAD 11 62373584 62373584 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:62373584C>T c.1607G>A c.(1606-1608)cGc>cAc p.R536H PAAD 11 62376231 62376231 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:62376231C>T c.976G>A c.(976-978)Gct>Act p.A326T PRAD 11 62370296 62370296 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:62370296C>T c.2422G>A c.(2422-2424)Gtg>Atg p.V808M PRAD 11 62375178 62375178 + Missense_Mutation SNP G G A TCGA-V1-A8ML-01A-11D-A377-08 TCGA-V1-A8ML-10A-01D-A37A-08 g.chr11:62375178G>A c.1322C>T c.(1321-1323)cCt>cTt p.P441L PRAD 11 62378665 62378665 + Missense_Mutation SNP G G A TCGA-CH-5791-01A-11D-1576-08 TCGA-CH-5791-10A-01D-1576-08 g.chr11:62378665G>A c.346C>T c.(346-348)Cct>Tct p.P116S SKCM 11 62372641 62372641 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:62372641G>A c.1926C>T c.(1924-1926)ctC>ctT p.L642L SKCM 11 62373192 62373192 + Missense_Mutation SNP G G T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:62373192G>T c.1836C>A c.(1834-1836)ttC>ttA p.F612L SKCM 11 62373339 62373339 + Silent SNP G G A TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr11:62373339G>A c.1770C>T c.(1768-1770)tcC>tcT p.S590S SKCM 11 62373563 62373563 + Missense_Mutation SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr11:62373563G>A c.1628C>T c.(1627-1629)cCc>cTc p.P543L SKCM 11 62373637 62373637 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:62373637G>A c.1554C>T c.(1552-1554)ttC>ttT p.F518F SKCM 11 62373637 62373637 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:62373637G>A c.1554C>T c.(1552-1554)ttC>ttT p.F518F SKCM 11 62375207 62375207 + Silent SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:62375207G>A c.1293C>T c.(1291-1293)ttC>ttT p.F431F SKCM 11 62375218 62375218 + Missense_Mutation SNP G G A TCGA-FW-A3TV-06A-11D-A23B-08 TCGA-FW-A3TV-10A-01D-A23B-08 g.chr11:62375218G>A c.1282C>T c.(1282-1284)Cac>Tac p.H428Y SKCM 11 62376026 62376026 + Silent SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr11:62376026G>A c.1098C>T c.(1096-1098)gcC>gcT p.A366A SKCM 11 62376050 62376050 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:62376050G>A c.1074C>T c.(1072-1074)ttC>ttT p.F358F SKCM 11 62376529 62376529 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:62376529G>A c.834C>T c.(832-834)gcC>gcT p.A278A SKCM 11 62376896 62376896 + Missense_Mutation SNP G G A TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr11:62376896G>A c.688C>T c.(688-690)Ccg>Tcg p.P230S SKCM 11 62376927 62376927 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:62376927G>A c.657C>T c.(655-657)ttC>ttT p.F219F SKCM 11 62377144 62377144 + Silent SNP G G A TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr11:62377144G>A c.591C>T c.(589-591)tcC>tcT p.S197S SKCM 11 62378444 62378444 + Missense_Mutation SNP G G A TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr11:62378444G>A c.473C>T c.(472-474)tCc>tTc p.S158F SKCM 11 62378686 62378686 + Missense_Mutation SNP G G A TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr11:62378686G>A c.325C>T c.(325-327)Cct>Tct p.P109S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 11 62366081 62366081 single base substitution C T downstream_gene_variant BLCA-CN 11 62367640 62367640 single base substitution G A downstream_gene_variant BLCA-CN 11 62384214 62384214 single base substitution G A upstream_gene_variant BLCA-US 11 62372641 62372641 single base substitution G C 3_prime_UTR_variant BLCA-US 11 62372641 62372641 single base substitution G C downstream_gene_variant BLCA-US 11 62372641 62372641 single base substitution G C exon_variant BLCA-US 11 62372641 62372641 single base substitution G C synonymous_variant L425L 1275C>G BLCA-US 11 62372641 62372641 single base substitution G C synonymous_variant L614L 1842C>G BLCA-US 11 62372641 62372641 single base substitution G C synonymous_variant L635L 1905C>G BLCA-US 11 62372641 62372641 single base substitution G C synonymous_variant L642L 1926C>G BLCA-US 11 62372641 62372641 single base substitution G C synonymous_variant L643L 1929C>G BLCA-US 11 62372641 62372641 single base substitution G C upstream_gene_variant BLCA-US 11 62376050 62376050 single base substitution G A 3_prime_UTR_variant BLCA-US 11 62376050 62376050 single base substitution G A downstream_gene_variant BLCA-US 11 62376050 62376050 single base substitution G A synonymous_variant F141F 423C>T BLCA-US 11 62376050 62376050 single base substitution G A synonymous_variant F330F 990C>T BLCA-US 11 62376050 62376050 single base substitution G A synonymous_variant F351F 1053C>T BLCA-US 11 62376050 62376050 single base substitution G A synonymous_variant F358F 1074C>T BLCA-US 11 62376050 62376050 single base substitution G A synonymous_variant F359F 1077C>T BLCA-US 11 62376050 62376050 single base substitution G A upstream_gene_variant BLCA-US 11 62378418 62378418 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BLCA-US 11 62378418 62378418 single base substitution G A downstream_gene_variant BLCA-US 11 62378418 62378418 single base substitution G A exon_variant BLCA-US 11 62378418 62378418 single base substitution G A missense_variant R139W 415C>T BLCA-US 11 62378418 62378418 single base substitution G A missense_variant R160W 478C>T BLCA-US 11 62378418 62378418 single base substitution G A missense_variant R167W 499C>T BLCA-US 11 62378418 62378418 single base substitution G A missense_variant R168W 502C>T BLCA-US 11 62378418 62378418 single base substitution G A upstream_gene_variant BLCA-US 11 62378910 62378910 single base substitution G A exon_variant BLCA-US 11 62378910 62378910 single base substitution G A missense_variant P32S 94C>T BLCA-US 11 62378910 62378910 single base substitution G A missense_variant P53S 157C>T BLCA-US 11 62378910 62378910 single base substitution G A missense_variant P61S 181C>T BLCA-US 11 62378910 62378910 single base substitution G A upstream_gene_variant BLCA-US 11 62384199 62384199 single base substitution G C upstream_gene_variant BRCA-EU 11 62365788 62365788 single base substitution C G downstream_gene_variant BRCA-EU 11 62366776 62366776 insertion of <=200bp - G downstream_gene_variant BRCA-EU 11 62366833 62366833 single base substitution T A downstream_gene_variant BRCA-EU 11 62367685 62367685 single base substitution C T downstream_gene_variant BRCA-EU 11 62367771 62367771 single base substitution G C downstream_gene_variant BRCA-EU 11 62370922 62370922 single base substitution C T downstream_gene_variant BRCA-EU 11 62370922 62370922 single base substitution C T intron_variant BRCA-EU 11 62371923 62371923 single base substitution C T downstream_gene_variant BRCA-EU 11 62371923 62371923 single base substitution C T intron_variant BRCA-EU 11 62371923 62371923 single base substitution C T upstream_gene_variant BRCA-EU 11 62372934 62372934 single base substitution C A downstream_gene_variant BRCA-EU 11 62372934 62372934 single base substitution C A intron_variant BRCA-EU 11 62372934 62372934 single base substitution C A upstream_gene_variant BRCA-EU 11 62374494 62374494 insertion of <=200bp - C 3_prime_UTR_variant BRCA-EU 11 62374494 62374494 insertion of <=200bp - C downstream_gene_variant BRCA-EU 11 62374494 62374494 insertion of <=200bp - C exon_variant BRCA-EU 11 62374494 62374494 insertion of <=200bp - C frameshift_variant G263G? BRCA-EU 11 62374494 62374494 insertion of <=200bp - C frameshift_variant G452G? BRCA-EU 11 62374494 62374494 insertion of <=200bp - C frameshift_variant G473G? BRCA-EU 11 62374494 62374494 insertion of <=200bp - C frameshift_variant G480G? BRCA-EU 11 62374494 62374494 insertion of <=200bp - C frameshift_variant G481G? BRCA-EU 11 62374494 62374494 insertion of <=200bp - C upstream_gene_variant BRCA-EU 11 62374928 62374928 single base substitution G C downstream_gene_variant BRCA-EU 11 62374928 62374928 single base substitution G C intron_variant BRCA-EU 11 62374928 62374928 single base substitution G C upstream_gene_variant BRCA-EU 11 62376044 62376044 single base substitution C A 3_prime_UTR_variant BRCA-EU 11 62376044 62376044 single base substitution C A downstream_gene_variant BRCA-EU 11 62376044 62376044 single base substitution C A synonymous_variant R143R 429G>T BRCA-EU 11 62376044 62376044 single base substitution C A synonymous_variant R332R 996G>T BRCA-EU 11 62376044 62376044 single base substitution C A synonymous_variant R353R 1059G>T BRCA-EU 11 62376044 62376044 single base substitution C A synonymous_variant R360R 1080G>T BRCA-EU 11 62376044 62376044 single base substitution C A synonymous_variant R361R 1083G>T BRCA-EU 11 62376044 62376044 single base substitution C A upstream_gene_variant BRCA-EU 11 62376885 62376885 single base substitution G A downstream_gene_variant BRCA-EU 11 62376885 62376885 single base substitution G A exon_variant BRCA-EU 11 62376885 62376885 single base substitution G A synonymous_variant I16I 48C>T BRCA-EU 11 62376885 62376885 single base substitution G A synonymous_variant I205I 615C>T BRCA-EU 11 62376885 62376885 single base substitution G A synonymous_variant I226I 678C>T BRCA-EU 11 62376885 62376885 single base substitution G A synonymous_variant I233I 699C>T BRCA-EU 11 62376885 62376885 single base substitution G A synonymous_variant I234I 702C>T BRCA-EU 11 62376885 62376885 single base substitution G A upstream_gene_variant BRCA-EU 11 62376892 62376892 single base substitution G A downstream_gene_variant BRCA-EU 11 62376892 62376892 single base substitution G A exon_variant BRCA-EU 11 62376892 62376892 single base substitution G A missense_variant S14F 41C>T BRCA-EU 11 62376892 62376892 single base substitution G A missense_variant S203F 608C>T BRCA-EU 11 62376892 62376892 single base substitution G A missense_variant S224F 671C>T BRCA-EU 11 62376892 62376892 single base substitution G A missense_variant S231F 692C>T BRCA-EU 11 62376892 62376892 single base substitution G A missense_variant S232F 695C>T BRCA-EU 11 62376892 62376892 single base substitution G A upstream_gene_variant BRCA-EU 11 62377213 62377213 single base substitution G A downstream_gene_variant BRCA-EU 11 62377213 62377213 single base substitution G A intron_variant BRCA-EU 11 62377213 62377213 single base substitution G A upstream_gene_variant BRCA-EU 11 62377349 62377349 single base substitution G A downstream_gene_variant BRCA-EU 11 62377349 62377349 single base substitution G A intron_variant BRCA-EU 11 62377349 62377349 single base substitution G A upstream_gene_variant BRCA-EU 11 62377356 62377356 single base substitution G A downstream_gene_variant BRCA-EU 11 62377356 62377356 single base substitution G A intron_variant BRCA-EU 11 62377356 62377356 single base substitution G A upstream_gene_variant BRCA-EU 11 62378732 62378732 single base substitution G T exon_variant BRCA-EU 11 62378732 62378732 single base substitution G T synonymous_variant L64L 192C>A BRCA-EU 11 62378732 62378732 single base substitution G T synonymous_variant L65L 195C>A BRCA-EU 11 62378732 62378732 single base substitution G T synonymous_variant L86L 258C>A BRCA-EU 11 62378732 62378732 single base substitution G T synonymous_variant L93L 279C>A BRCA-EU 11 62378732 62378732 single base substitution G T synonymous_variant L94L 282C>A BRCA-EU 11 62378732 62378732 single base substitution G T upstream_gene_variant BRCA-EU 11 62379598 62379598 single base substitution G C 5_prime_UTR_variant BRCA-EU 11 62379598 62379598 single base substitution G C intron_variant BRCA-EU 11 62379598 62379598 single base substitution G C upstream_gene_variant BRCA-EU 11 62380203 62380203 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 11 62380203 62380203 single base substitution G A upstream_gene_variant BRCA-EU 11 62383717 62383717 single base substitution A C upstream_gene_variant BRCA-EU 11 62384539 62384539 single base substitution C T upstream_gene_variant BRCA-FR 11 62365788 62365788 single base substitution C G downstream_gene_variant BRCA-FR 11 62366833 62366833 single base substitution T A downstream_gene_variant BRCA-FR 11 62367075 62367075 single base substitution A T downstream_gene_variant BRCA-FR 11 62371923 62371923 single base substitution C T downstream_gene_variant BRCA-FR 11 62371923 62371923 single base substitution C T intron_variant BRCA-FR 11 62371923 62371923 single base substitution C T upstream_gene_variant BRCA-UK 11 62372934 62372934 single base substitution C A downstream_gene_variant BRCA-UK 11 62372934 62372934 single base substitution C A intron_variant BRCA-UK 11 62372934 62372934 single base substitution C A upstream_gene_variant BRCA-UK 11 62376840 62376840 single base substitution G C 3_prime_UTR_variant BRCA-UK 11 62376840 62376840 single base substitution G C downstream_gene_variant BRCA-UK 11 62376840 62376840 single base substitution G C synonymous_variant L220L 660C>G BRCA-UK 11 62376840 62376840 single base substitution G C synonymous_variant L241L 723C>G BRCA-UK 11 62376840 62376840 single base substitution G C synonymous_variant L248L 744C>G BRCA-UK 11 62376840 62376840 single base substitution G C synonymous_variant L249L 747C>G BRCA-UK 11 62376840 62376840 single base substitution G C synonymous_variant L31L 93C>G BRCA-UK 11 62376840 62376840 single base substitution G C upstream_gene_variant BRCA-US 11 62365548 62365548 single base substitution C T downstream_gene_variant BRCA-US 11 62365556 62365556 single base substitution G A downstream_gene_variant BRCA-US 11 62365601 62365601 deletion of <=200bp A - downstream_gene_variant BRCA-US 11 62367698 62367699 deletion of <=200bp AG - downstream_gene_variant BRCA-US 11 62370688 62370688 single base substitution C A 3_prime_UTR_variant BRCA-US 11 62370688 62370688 single base substitution C A downstream_gene_variant BRCA-US 11 62370688 62370688 single base substitution C A exon_variant BRCA-US 11 62370688 62370688 single base substitution C A missense_variant K14N 42G>T BRCA-US 11 62370688 62370688 single base substitution C A missense_variant K546N 1638G>T BRCA-US 11 62370688 62370688 single base substitution C A missense_variant K735N 2205G>T BRCA-US 11 62370688 62370688 single base substitution C A missense_variant K756N 2268G>T BRCA-US 11 62370688 62370688 single base substitution C A missense_variant K763N 2289G>T BRCA-US 11 62370688 62370688 single base substitution C A missense_variant K764N 2292G>T BRCA-US 11 62371661 62371661 single base substitution C T 3_prime_UTR_variant BRCA-US 11 62371661 62371661 single base substitution C T downstream_gene_variant BRCA-US 11 62371661 62371661 single base substitution C T exon_variant BRCA-US 11 62371661 62371661 single base substitution C T synonymous_variant L448L 1344G>A BRCA-US 11 62371661 62371661 single base substitution C T synonymous_variant L637L 1911G>A BRCA-US 11 62371661 62371661 single base substitution C T synonymous_variant L658L 1974G>A BRCA-US 11 62371661 62371661 single base substitution C T synonymous_variant L665L 1995G>A BRCA-US 11 62371661 62371661 single base substitution C T synonymous_variant L666L 1998G>A BRCA-US 11 62371661 62371661 single base substitution C T upstream_gene_variant BRCA-US 11 62376502 62376502 single base substitution T C 3_prime_UTR_variant BRCA-US 11 62376502 62376502 single base substitution T C downstream_gene_variant BRCA-US 11 62376502 62376502 single base substitution T C synonymous_variant G259G 777A>G BRCA-US 11 62376502 62376502 single base substitution T C synonymous_variant G280G 840A>G BRCA-US 11 62376502 62376502 single base substitution T C synonymous_variant G287G 861A>G BRCA-US 11 62376502 62376502 single base substitution T C synonymous_variant G288G 864A>G BRCA-US 11 62376502 62376502 single base substitution T C synonymous_variant G70G 210A>G BRCA-US 11 62376502 62376502 single base substitution T C upstream_gene_variant BRCA-US 11 62378355 62378355 single base substitution C T 5_prime_UTR_variant BRCA-US 11 62378355 62378355 single base substitution C T downstream_gene_variant BRCA-US 11 62378355 62378355 single base substitution C T exon_variant BRCA-US 11 62378355 62378355 single base substitution C T missense_variant E160K 478G>A BRCA-US 11 62378355 62378355 single base substitution C T missense_variant E181K 541G>A BRCA-US 11 62378355 62378355 single base substitution C T missense_variant E188K 562G>A BRCA-US 11 62378355 62378355 single base substitution C T missense_variant E189K 565G>A BRCA-US 11 62378355 62378355 single base substitution C T upstream_gene_variant BRCA-US 11 62378386 62378386 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 11 62378386 62378386 single base substitution G A downstream_gene_variant BRCA-US 11 62378386 62378386 single base substitution G A exon_variant BRCA-US 11 62378386 62378386 single base substitution G A synonymous_variant S149S 447C>T BRCA-US 11 62378386 62378386 single base substitution G A synonymous_variant S170S 510C>T BRCA-US 11 62378386 62378386 single base substitution G A synonymous_variant S177S 531C>T BRCA-US 11 62378386 62378386 single base substitution G A synonymous_variant S178S 534C>T BRCA-US 11 62378386 62378386 single base substitution G A upstream_gene_variant BRCA-US 11 62378801 62378801 insertion of <=200bp - G exon_variant BRCA-US 11 62378801 62378801 insertion of <=200bp - G frameshift_variant P41P? BRCA-US 11 62378801 62378801 insertion of <=200bp - G frameshift_variant P42P? BRCA-US 11 62378801 62378801 insertion of <=200bp - G frameshift_variant P63P? BRCA-US 11 62378801 62378801 insertion of <=200bp - G frameshift_variant P70P? BRCA-US 11 62378801 62378801 insertion of <=200bp - G frameshift_variant P71P? BRCA-US 11 62378801 62378801 insertion of <=200bp - G upstream_gene_variant BRCA-US 11 62381027 62381027 single base substitution C G upstream_gene_variant BRCA-US 11 62381062 62381062 single base substitution G T upstream_gene_variant BRCA-US 11 62381084 62381084 deletion of <=200bp G - upstream_gene_variant BRCA-US 11 62383253 62383253 single base substitution G A upstream_gene_variant BTCA-JP 11 62365550 62365550 single base substitution C T downstream_gene_variant BTCA-JP 11 62366030 62366030 single base substitution G A downstream_gene_variant BTCA-JP 11 62367914 62367914 single base substitution C A downstream_gene_variant BTCA-JP 11 62368803 62368803 single base substitution G A downstream_gene_variant BTCA-JP 11 62370817 62370817 single base substitution C T downstream_gene_variant BTCA-JP 11 62370817 62370817 single base substitution C T intron_variant BTCA-JP 11 62372631 62372631 single base substitution A C 3_prime_UTR_variant BTCA-JP 11 62372631 62372631 single base substitution A C downstream_gene_variant BTCA-JP 11 62372631 62372631 single base substitution A C exon_variant BTCA-JP 11 62372631 62372631 single base substitution A C missense_variant F429V 1285T>G BTCA-JP 11 62372631 62372631 single base substitution A C missense_variant F618V 1852T>G BTCA-JP 11 62372631 62372631 single base substitution A C missense_variant F639V 1915T>G BTCA-JP 11 62372631 62372631 single base substitution A C missense_variant F646V 1936T>G BTCA-JP 11 62372631 62372631 single base substitution A C missense_variant F647V 1939T>G BTCA-JP 11 62372631 62372631 single base substitution A C upstream_gene_variant BTCA-JP 11 62373651 62373651 single base substitution C T 3_prime_UTR_variant BTCA-JP 11 62373651 62373651 single base substitution C T downstream_gene_variant BTCA-JP 11 62373651 62373651 single base substitution C T exon_variant BTCA-JP 11 62373651 62373651 single base substitution C T missense_variant E297K 889G>A BTCA-JP 11 62373651 62373651 single base substitution C T missense_variant E486K 1456G>A BTCA-JP 11 62373651 62373651 single base substitution C T missense_variant E507K 1519G>A BTCA-JP 11 62373651 62373651 single base substitution C T missense_variant E514K 1540G>A BTCA-JP 11 62373651 62373651 single base substitution C T missense_variant E515K 1543G>A BTCA-JP 11 62373651 62373651 single base substitution C T upstream_gene_variant BTCA-JP 11 62375757 62375757 single base substitution G T 3_prime_UTR_variant BTCA-JP 11 62375757 62375757 single base substitution G T downstream_gene_variant BTCA-JP 11 62375757 62375757 single base substitution G T synonymous_variant A157A 471C>A BTCA-JP 11 62375757 62375757 single base substitution G T synonymous_variant A346A 1038C>A BTCA-JP 11 62375757 62375757 single base substitution G T synonymous_variant A367A 1101C>A BTCA-JP 11 62375757 62375757 single base substitution G T synonymous_variant A374A 1122C>A BTCA-JP 11 62375757 62375757 single base substitution G T synonymous_variant A375A 1125C>A BTCA-JP 11 62375757 62375757 single base substitution G T upstream_gene_variant BTCA-JP 11 62376896 62376896 single base substitution G T downstream_gene_variant BTCA-JP 11 62376896 62376896 single base substitution G T exon_variant BTCA-JP 11 62376896 62376896 single base substitution G T missense_variant P13T 37C>A BTCA-JP 11 62376896 62376896 single base substitution G T missense_variant P202T 604C>A BTCA-JP 11 62376896 62376896 single base substitution G T missense_variant P223T 667C>A BTCA-JP 11 62376896 62376896 single base substitution G T missense_variant P230T 688C>A BTCA-JP 11 62376896 62376896 single base substitution G T missense_variant P231T 691C>A BTCA-JP 11 62376896 62376896 single base substitution G T upstream_gene_variant BTCA-JP 11 62377221 62377221 single base substitution C A downstream_gene_variant BTCA-JP 11 62377221 62377221 single base substitution C A intron_variant BTCA-JP 11 62377221 62377221 single base substitution C A upstream_gene_variant BTCA-JP 11 62378671 62378671 single base substitution C G exon_variant BTCA-JP 11 62378671 62378671 single base substitution C G missense_variant E107Q 319G>C BTCA-JP 11 62378671 62378671 single base substitution C G missense_variant E114Q 340G>C BTCA-JP 11 62378671 62378671 single base substitution C G missense_variant E115Q 343G>C BTCA-JP 11 62378671 62378671 single base substitution C G missense_variant E85Q 253G>C BTCA-JP 11 62378671 62378671 single base substitution C G missense_variant E86Q 256G>C BTCA-JP 11 62378671 62378671 single base substitution C G upstream_gene_variant BTCA-JP 11 62381084 62381084 deletion of <=200bp G - upstream_gene_variant BTCA-JP 11 62381251 62381251 single base substitution C T upstream_gene_variant BTCA-JP 11 62381422 62381422 single base substitution G A upstream_gene_variant BTCA-JP 11 62381677 62381677 deletion of <=200bp C - upstream_gene_variant BTCA-JP 11 62383426 62383426 single base substitution C T upstream_gene_variant BTCA-JP 11 62383427 62383427 single base substitution C T upstream_gene_variant CESC-US 11 62369823 62369823 single base substitution G A 3_prime_UTR_variant CESC-US 11 62369823 62369823 single base substitution G A downstream_gene_variant CESC-US 11 62369823 62369823 single base substitution G A exon_variant CESC-US 11 62369823 62369823 single base substitution G A missense_variant S874L 2621C>T CESC-US 11 62369823 62369823 single base substitution G A missense_variant S895L 2684C>T CESC-US 11 62369823 62369823 single base substitution G A missense_variant S902L 2705C>T CESC-US 11 62370341 62370341 single base substitution C T 3_prime_UTR_variant CESC-US 11 62370341 62370341 single base substitution C T downstream_gene_variant CESC-US 11 62370341 62370341 single base substitution C T exon_variant CESC-US 11 62370341 62370341 single base substitution C T intron_variant CESC-US 11 62370341 62370341 single base substitution C T missense_variant D576N 1726G>A CESC-US 11 62370341 62370341 single base substitution C T missense_variant D793N 2377G>A CESC-US 11 62370341 62370341 single base substitution C T missense_variant D794N 2380G>A CESC-US 11 62371633 62371633 single base substitution C T 3_prime_UTR_variant CESC-US 11 62371633 62371633 single base substitution C T downstream_gene_variant CESC-US 11 62371633 62371633 single base substitution C T exon_variant CESC-US 11 62371633 62371633 single base substitution C T missense_variant D458N 1372G>A CESC-US 11 62371633 62371633 single base substitution C T missense_variant D647N 1939G>A CESC-US 11 62371633 62371633 single base substitution C T missense_variant D668N 2002G>A CESC-US 11 62371633 62371633 single base substitution C T missense_variant D675N 2023G>A CESC-US 11 62371633 62371633 single base substitution C T missense_variant D676N 2026G>A CESC-US 11 62371633 62371633 single base substitution C T upstream_gene_variant CESC-US 11 62373588 62373588 single base substitution C G 3_prime_UTR_variant CESC-US 11 62373588 62373588 single base substitution C G downstream_gene_variant CESC-US 11 62373588 62373588 single base substitution C G exon_variant CESC-US 11 62373588 62373588 single base substitution C G missense_variant D318H 952G>C CESC-US 11 62373588 62373588 single base substitution C G missense_variant D507H 1519G>C CESC-US 11 62373588 62373588 single base substitution C G missense_variant D528H 1582G>C CESC-US 11 62373588 62373588 single base substitution C G missense_variant D535H 1603G>C CESC-US 11 62373588 62373588 single base substitution C G missense_variant D536H 1606G>C CESC-US 11 62373588 62373588 single base substitution C G upstream_gene_variant CESC-US 11 62376235 62376235 single base substitution C G 3_prime_UTR_variant CESC-US 11 62376235 62376235 single base substitution C G downstream_gene_variant CESC-US 11 62376235 62376235 single base substitution C G missense_variant Q107H 321G>C CESC-US 11 62376235 62376235 single base substitution C G missense_variant Q296H 888G>C CESC-US 11 62376235 62376235 single base substitution C G missense_variant Q317H 951G>C CESC-US 11 62376235 62376235 single base substitution C G missense_variant Q324H 972G>C CESC-US 11 62376235 62376235 single base substitution C G missense_variant Q325H 975G>C CESC-US 11 62376235 62376235 single base substitution C G upstream_gene_variant CESC-US 11 62384213 62384213 single base substitution C T upstream_gene_variant COAD-US 11 62365846 62365846 single base substitution T C downstream_gene_variant COAD-US 11 62365995 62365995 single base substitution G A downstream_gene_variant COAD-US 11 62367689 62367689 single base substitution G A downstream_gene_variant COAD-US 11 62376450 62376450 single base substitution T C 3_prime_UTR_variant COAD-US 11 62376450 62376450 single base substitution T C downstream_gene_variant COAD-US 11 62376450 62376450 single base substitution T C missense_variant T277A 829A>G COAD-US 11 62376450 62376450 single base substitution T C missense_variant T298A 892A>G COAD-US 11 62376450 62376450 single base substitution T C missense_variant T305A 913A>G COAD-US 11 62376450 62376450 single base substitution T C missense_variant T306A 916A>G COAD-US 11 62376450 62376450 single base substitution T C missense_variant T88A 262A>G COAD-US 11 62376450 62376450 single base substitution T C upstream_gene_variant COAD-US 11 62378798 62378798 insertion of <=200bp - C exon_variant COAD-US 11 62378798 62378798 insertion of <=200bp - C frameshift_variant G42G? COAD-US 11 62378798 62378798 insertion of <=200bp - C frameshift_variant G43G? COAD-US 11 62378798 62378798 insertion of <=200bp - C frameshift_variant G64G? COAD-US 11 62378798 62378798 insertion of <=200bp - C frameshift_variant G71G? COAD-US 11 62378798 62378798 insertion of <=200bp - C frameshift_variant G72G? COAD-US 11 62378798 62378798 insertion of <=200bp - C upstream_gene_variant COAD-US 11 62378802 62378802 deletion of <=200bp G - exon_variant COAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P41 COAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P42 COAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P63 COAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P70 COAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P71 COAD-US 11 62378802 62378802 deletion of <=200bp G - upstream_gene_variant COAD-US 11 62378942 62378942 deletion of <=200bp G - exon_variant COAD-US 11 62378942 62378942 deletion of <=200bp G - frameshift_variant P21 COAD-US 11 62378942 62378942 deletion of <=200bp G - frameshift_variant P42 COAD-US 11 62378942 62378942 deletion of <=200bp G - frameshift_variant P50 COAD-US 11 62378942 62378942 deletion of <=200bp G - upstream_gene_variant COAD-US 11 62381084 62381084 deletion of <=200bp G - upstream_gene_variant COAD-US 11 62381106 62381106 single base substitution G C upstream_gene_variant COAD-US 11 62381330 62381330 single base substitution C T upstream_gene_variant COAD-US 11 62381808 62381808 single base substitution G C upstream_gene_variant COAD-US 11 62383976 62383976 single base substitution A G upstream_gene_variant COAD-US 11 62384458 62384460 deletion of <=200bp CCT - upstream_gene_variant COCA-CN 11 62364789 62364789 single base substitution A G downstream_gene_variant COCA-CN 11 62365662 62365662 single base substitution G A downstream_gene_variant COCA-CN 11 62367608 62367608 single base substitution G T downstream_gene_variant COCA-CN 11 62373469 62373469 single base substitution G A downstream_gene_variant COCA-CN 11 62373469 62373469 single base substitution G A exon_variant COCA-CN 11 62373469 62373469 single base substitution G A intron_variant COCA-CN 11 62373469 62373469 single base substitution G A upstream_gene_variant COCA-CN 11 62374512 62374512 single base substitution G A 3_prime_UTR_variant COCA-CN 11 62374512 62374512 single base substitution G A downstream_gene_variant COCA-CN 11 62374512 62374512 single base substitution G A exon_variant COCA-CN 11 62374512 62374512 single base substitution G A synonymous_variant L257L 771C>T COCA-CN 11 62374512 62374512 single base substitution G A synonymous_variant L446L 1338C>T COCA-CN 11 62374512 62374512 single base substitution G A synonymous_variant L467L 1401C>T COCA-CN 11 62374512 62374512 single base substitution G A synonymous_variant L474L 1422C>T COCA-CN 11 62374512 62374512 single base substitution G A synonymous_variant L475L 1425C>T COCA-CN 11 62374512 62374512 single base substitution G A upstream_gene_variant COCA-CN 11 62375166 62375166 single base substitution G A 3_prime_UTR_variant COCA-CN 11 62375166 62375166 single base substitution G A downstream_gene_variant COCA-CN 11 62375166 62375166 single base substitution G A intron_variant COCA-CN 11 62375166 62375166 single base substitution G A missense_variant T228I 683C>T COCA-CN 11 62375166 62375166 single base substitution G A missense_variant T417I 1250C>T COCA-CN 11 62375166 62375166 single base substitution G A missense_variant T438I 1313C>T COCA-CN 11 62375166 62375166 single base substitution G A missense_variant T445I 1334C>T COCA-CN 11 62375166 62375166 single base substitution G A missense_variant T446I 1337C>T COCA-CN 11 62375166 62375166 single base substitution G A upstream_gene_variant COCA-CN 11 62379041 62379041 single base substitution T G 5_prime_UTR_variant COCA-CN 11 62379041 62379041 single base substitution T G missense_variant Q17P 50A>C COCA-CN 11 62379041 62379041 single base substitution T G missense_variant Q9P 26A>C COCA-CN 11 62379041 62379041 single base substitution T G upstream_gene_variant COCA-CN 11 62379055 62379055 single base substitution A G 5_prime_UTR_variant COCA-CN 11 62379055 62379055 single base substitution A G synonymous_variant A12A 36T>C COCA-CN 11 62379055 62379055 single base substitution A G synonymous_variant A4A 12T>C COCA-CN 11 62379055 62379055 single base substitution A G upstream_gene_variant COCA-CN 11 62379080 62379080 single base substitution G A 5_prime_UTR_variant COCA-CN 11 62379080 62379080 single base substitution G A intron_variant COCA-CN 11 62379080 62379080 single base substitution G A upstream_gene_variant COCA-CN 11 62381101 62381101 single base substitution C T upstream_gene_variant COCA-CN 11 62381270 62381270 single base substitution G A upstream_gene_variant COCA-CN 11 62381898 62381898 single base substitution C T upstream_gene_variant COCA-CN 11 62383716 62383716 single base substitution A C upstream_gene_variant COCA-CN 11 62383717 62383717 single base substitution A C upstream_gene_variant COCA-CN 11 62383718 62383718 single base substitution A C upstream_gene_variant COCA-CN 11 62384360 62384360 single base substitution C T upstream_gene_variant COCA-CN 11 62384421 62384421 single base substitution G A upstream_gene_variant EOPC-DE 11 62382400 62382400 single base substitution C T upstream_gene_variant ESAD-UK 11 62364888 62364888 single base substitution C T downstream_gene_variant ESAD-UK 11 62365414 62365414 single base substitution G T downstream_gene_variant ESAD-UK 11 62370434 62370434 single base substitution G A downstream_gene_variant ESAD-UK 11 62370434 62370434 single base substitution G A exon_variant ESAD-UK 11 62370434 62370434 single base substitution G A intron_variant ESAD-UK 11 62372170 62372170 single base substitution G A downstream_gene_variant ESAD-UK 11 62372170 62372170 single base substitution G A intron_variant ESAD-UK 11 62372170 62372170 single base substitution G A upstream_gene_variant ESAD-UK 11 62374796 62374796 single base substitution C T downstream_gene_variant ESAD-UK 11 62374796 62374796 single base substitution C T exon_variant ESAD-UK 11 62374796 62374796 single base substitution C T intron_variant ESAD-UK 11 62374796 62374796 single base substitution C T upstream_gene_variant ESAD-UK 11 62374922 62374922 single base substitution T C downstream_gene_variant ESAD-UK 11 62374922 62374922 single base substitution T C intron_variant ESAD-UK 11 62374922 62374922 single base substitution T C upstream_gene_variant ESAD-UK 11 62375750 62375750 single base substitution A G 3_prime_UTR_variant ESAD-UK 11 62375750 62375750 single base substitution A G downstream_gene_variant ESAD-UK 11 62375750 62375750 single base substitution A G missense_variant C160R 478T>C ESAD-UK 11 62375750 62375750 single base substitution A G missense_variant C349R 1045T>C ESAD-UK 11 62375750 62375750 single base substitution A G missense_variant C370R 1108T>C ESAD-UK 11 62375750 62375750 single base substitution A G missense_variant C377R 1129T>C ESAD-UK 11 62375750 62375750 single base substitution A G missense_variant C378R 1132T>C ESAD-UK 11 62375750 62375750 single base substitution A G upstream_gene_variant ESAD-UK 11 62377122 62377122 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 11 62377122 62377122 single base substitution G A downstream_gene_variant ESAD-UK 11 62377122 62377122 single base substitution G A exon_variant ESAD-UK 11 62377122 62377122 single base substitution G A missense_variant R177W 529C>T ESAD-UK 11 62377122 62377122 single base substitution G A missense_variant R198W 592C>T ESAD-UK 11 62377122 62377122 single base substitution G A missense_variant R205W 613C>T ESAD-UK 11 62377122 62377122 single base substitution G A missense_variant R206W 616C>T ESAD-UK 11 62377122 62377122 single base substitution G A upstream_gene_variant ESAD-UK 11 62380567 62380567 single base substitution G A upstream_gene_variant ESAD-UK 11 62384993 62384993 single base substitution T A upstream_gene_variant ESCA-CN 11 62374470 62374470 single base substitution G A 3_prime_UTR_variant ESCA-CN 11 62374470 62374470 single base substitution G A downstream_gene_variant ESCA-CN 11 62374470 62374470 single base substitution G A exon_variant ESCA-CN 11 62374470 62374470 single base substitution G A synonymous_variant S271S 813C>T ESCA-CN 11 62374470 62374470 single base substitution G A synonymous_variant S460S 1380C>T ESCA-CN 11 62374470 62374470 single base substitution G A synonymous_variant S481S 1443C>T ESCA-CN 11 62374470 62374470 single base substitution G A synonymous_variant S488S 1464C>T ESCA-CN 11 62374470 62374470 single base substitution G A synonymous_variant S489S 1467C>T ESCA-CN 11 62374470 62374470 single base substitution G A upstream_gene_variant ESCA-CN 11 62376473 62376473 single base substitution C T 3_prime_UTR_variant ESCA-CN 11 62376473 62376473 single base substitution C T downstream_gene_variant ESCA-CN 11 62376473 62376473 single base substitution C T missense_variant G269D 806G>A ESCA-CN 11 62376473 62376473 single base substitution C T missense_variant G290D 869G>A ESCA-CN 11 62376473 62376473 single base substitution C T missense_variant G297D 890G>A ESCA-CN 11 62376473 62376473 single base substitution C T missense_variant G298D 893G>A ESCA-CN 11 62376473 62376473 single base substitution C T missense_variant G80D 239G>A ESCA-CN 11 62376473 62376473 single base substitution C T upstream_gene_variant ESCA-CN 11 62378450 62378450 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant ESCA-CN 11 62378450 62378450 single base substitution G C downstream_gene_variant ESCA-CN 11 62378450 62378450 single base substitution G C intron_variant ESCA-CN 11 62378450 62378450 single base substitution G C missense_variant S127C 380C>G ESCA-CN 11 62378450 62378450 single base substitution G C missense_variant S128C 383C>G ESCA-CN 11 62378450 62378450 single base substitution G C missense_variant S149C 446C>G ESCA-CN 11 62378450 62378450 single base substitution G C missense_variant S156C 467C>G ESCA-CN 11 62378450 62378450 single base substitution G C missense_variant S157C 470C>G ESCA-CN 11 62378450 62378450 single base substitution G C upstream_gene_variant GBM-US 11 62378668 62378668 single base substitution C A exon_variant GBM-US 11 62378668 62378668 single base substitution C A stop_gained E108* 322G>T GBM-US 11 62378668 62378668 single base substitution C A stop_gained E115* 343G>T GBM-US 11 62378668 62378668 single base substitution C A stop_gained E116* 346G>T GBM-US 11 62378668 62378668 single base substitution C A stop_gained E86* 256G>T GBM-US 11 62378668 62378668 single base substitution C A stop_gained E87* 259G>T GBM-US 11 62378668 62378668 single base substitution C A upstream_gene_variant KIRC-US 11 62366080 62366080 single base substitution C G downstream_gene_variant KIRC-US 11 62373575 62373575 single base substitution A C 3_prime_UTR_variant KIRC-US 11 62373575 62373575 single base substitution A C downstream_gene_variant KIRC-US 11 62373575 62373575 single base substitution A C exon_variant KIRC-US 11 62373575 62373575 single base substitution A C missense_variant V322G 965T>G KIRC-US 11 62373575 62373575 single base substitution A C missense_variant V511G 1532T>G KIRC-US 11 62373575 62373575 single base substitution A C missense_variant V532G 1595T>G KIRC-US 11 62373575 62373575 single base substitution A C missense_variant V539G 1616T>G KIRC-US 11 62373575 62373575 single base substitution A C missense_variant V540G 1619T>G KIRC-US 11 62373575 62373575 single base substitution A C upstream_gene_variant KIRC-US 11 62381083 62381083 deletion of <=200bp T - upstream_gene_variant KIRC-US 11 62384532 62384532 single base substitution G A upstream_gene_variant LAML-KR 11 62369884 62369884 single base substitution C G 3_prime_UTR_variant LAML-KR 11 62369884 62369884 single base substitution C G downstream_gene_variant LAML-KR 11 62369884 62369884 single base substitution C G exon_variant LAML-KR 11 62369884 62369884 single base substitution C G missense_variant A854P 2560G>C LAML-KR 11 62369884 62369884 single base substitution C G missense_variant A875P 2623G>C LAML-KR 11 62369884 62369884 single base substitution C G missense_variant A882P 2644G>C LAML-KR 11 62374584 62374584 single base substitution G A downstream_gene_variant LAML-KR 11 62374584 62374584 single base substitution G A exon_variant LAML-KR 11 62374584 62374584 single base substitution G A intron_variant LAML-KR 11 62374584 62374584 single base substitution G A upstream_gene_variant LAML-KR 11 62379037 62379037 single base substitution A G 5_prime_UTR_variant LAML-KR 11 62379037 62379037 single base substitution A G synonymous_variant S10S 30T>C LAML-KR 11 62379037 62379037 single base substitution A G synonymous_variant S18S 54T>C LAML-KR 11 62379037 62379037 single base substitution A G upstream_gene_variant LGG-US 11 62380964 62380964 single base substitution G A upstream_gene_variant LGG-US 11 62381890 62381890 single base substitution C T upstream_gene_variant LICA-CN 11 62367654 62367654 single base substitution C A downstream_gene_variant LICA-CN 11 62369996 62369996 single base substitution G T 3_prime_UTR_variant LICA-CN 11 62369996 62369996 single base substitution G T downstream_gene_variant LICA-CN 11 62369996 62369996 single base substitution G T exon_variant LICA-CN 11 62369996 62369996 single base substitution G T missense_variant H816Q 2448C>A LICA-CN 11 62369996 62369996 single base substitution G T missense_variant H837Q 2511C>A LICA-CN 11 62369996 62369996 single base substitution G T missense_variant H844Q 2532C>A LICA-CN 11 62369996 62369996 single base substitution G T missense_variant T122K 365C>A LICA-CN 11 62369996 62369996 single base substitution G T missense_variant T664K 1991C>A LICA-CN 11 62369996 62369996 single base substitution G T missense_variant T881K 2642C>A LICA-CN 11 62369996 62369996 single base substitution G T missense_variant T882K 2645C>A LICA-CN 11 62371446 62371446 single base substitution A T 3_prime_UTR_variant LICA-CN 11 62371446 62371446 single base substitution A T downstream_gene_variant LICA-CN 11 62371446 62371446 single base substitution A T exon_variant LICA-CN 11 62371446 62371446 single base substitution A T synonymous_variant G496G 1488T>A LICA-CN 11 62371446 62371446 single base substitution A T synonymous_variant G685G 2055T>A LICA-CN 11 62371446 62371446 single base substitution A T synonymous_variant G706G 2118T>A LICA-CN 11 62371446 62371446 single base substitution A T synonymous_variant G713G 2139T>A LICA-CN 11 62371446 62371446 single base substitution A T synonymous_variant G714G 2142T>A LICA-CN 11 62371446 62371446 single base substitution A T upstream_gene_variant LICA-FR 11 62364796 62364796 single base substitution T C downstream_gene_variant LICA-FR 11 62370313 62370313 single base substitution C T 3_prime_UTR_variant LICA-FR 11 62370313 62370313 single base substitution C T downstream_gene_variant LICA-FR 11 62370313 62370313 single base substitution C T exon_variant LICA-FR 11 62370313 62370313 single base substitution C T intron_variant LICA-FR 11 62370313 62370313 single base substitution C T missense_variant R585H 1754G>A LICA-FR 11 62370313 62370313 single base substitution C T missense_variant R802H 2405G>A LICA-FR 11 62370313 62370313 single base substitution C T missense_variant R803H 2408G>A LICA-FR 11 62378406 62378406 single base substitution A C 5_prime_UTR_variant LICA-FR 11 62378406 62378406 single base substitution A C downstream_gene_variant LICA-FR 11 62378406 62378406 single base substitution A C exon_variant LICA-FR 11 62378406 62378406 single base substitution A C missense_variant S143A 427T>G LICA-FR 11 62378406 62378406 single base substitution A C missense_variant S164A 490T>G LICA-FR 11 62378406 62378406 single base substitution A C missense_variant S171A 511T>G LICA-FR 11 62378406 62378406 single base substitution A C missense_variant S172A 514T>G LICA-FR 11 62378406 62378406 single base substitution A C upstream_gene_variant LICA-FR 11 62382562 62382562 single base substitution T C upstream_gene_variant LICA-FR 11 62384122 62384122 single base substitution T C upstream_gene_variant LIHC-US 11 62370651 62370651 single base substitution A G 3_prime_UTR_variant LIHC-US 11 62370651 62370651 single base substitution A G downstream_gene_variant LIHC-US 11 62370651 62370651 single base substitution A G exon_variant LIHC-US 11 62370651 62370651 single base substitution A G missense_variant Y27H 79T>C LIHC-US 11 62370651 62370651 single base substitution A G missense_variant Y559H 1675T>C LIHC-US 11 62370651 62370651 single base substitution A G missense_variant Y748H 2242T>C LIHC-US 11 62370651 62370651 single base substitution A G missense_variant Y769H 2305T>C LIHC-US 11 62370651 62370651 single base substitution A G missense_variant Y776H 2326T>C LIHC-US 11 62370651 62370651 single base substitution A G missense_variant Y777H 2329T>C LIHC-US 11 62373664 62373664 single base substitution C T 3_prime_UTR_variant LIHC-US 11 62373664 62373664 single base substitution C T downstream_gene_variant LIHC-US 11 62373664 62373664 single base substitution C T exon_variant LIHC-US 11 62373664 62373664 single base substitution C T synonymous_variant Q292Q 876G>A LIHC-US 11 62373664 62373664 single base substitution C T synonymous_variant Q481Q 1443G>A LIHC-US 11 62373664 62373664 single base substitution C T synonymous_variant Q502Q 1506G>A LIHC-US 11 62373664 62373664 single base substitution C T synonymous_variant Q509Q 1527G>A LIHC-US 11 62373664 62373664 single base substitution C T synonymous_variant Q510Q 1530G>A LIHC-US 11 62373664 62373664 single base substitution C T upstream_gene_variant LIHC-US 11 62375693 62375693 single base substitution T C 3_prime_UTR_variant LIHC-US 11 62375693 62375693 single base substitution T C downstream_gene_variant LIHC-US 11 62375693 62375693 single base substitution T C missense_variant M179V 535A>G LIHC-US 11 62375693 62375693 single base substitution T C missense_variant M368V 1102A>G LIHC-US 11 62375693 62375693 single base substitution T C missense_variant M389V 1165A>G LIHC-US 11 62375693 62375693 single base substitution T C missense_variant M396V 1186A>G LIHC-US 11 62375693 62375693 single base substitution T C missense_variant M397V 1189A>G LIHC-US 11 62375693 62375693 single base substitution T C upstream_gene_variant LIHC-US 11 62376466 62376466 single base substitution T C 3_prime_UTR_variant LIHC-US 11 62376466 62376466 single base substitution T C downstream_gene_variant LIHC-US 11 62376466 62376466 single base substitution T C synonymous_variant R271R 813A>G LIHC-US 11 62376466 62376466 single base substitution T C synonymous_variant R292R 876A>G LIHC-US 11 62376466 62376466 single base substitution T C synonymous_variant R299R 897A>G LIHC-US 11 62376466 62376466 single base substitution T C synonymous_variant R300R 900A>G LIHC-US 11 62376466 62376466 single base substitution T C synonymous_variant R82R 246A>G LIHC-US 11 62376466 62376466 single base substitution T C upstream_gene_variant LIHC-US 11 62384649 62384649 single base substitution T A upstream_gene_variant LINC-JP 11 62376116 62376116 single base substitution C T 3_prime_UTR_variant LINC-JP 11 62376116 62376116 single base substitution C T downstream_gene_variant LINC-JP 11 62376116 62376116 single base substitution C T synonymous_variant Q119Q 357G>A LINC-JP 11 62376116 62376116 single base substitution C T synonymous_variant Q308Q 924G>A LINC-JP 11 62376116 62376116 single base substitution C T synonymous_variant Q329Q 987G>A LINC-JP 11 62376116 62376116 single base substitution C T synonymous_variant Q336Q 1008G>A LINC-JP 11 62376116 62376116 single base substitution C T synonymous_variant Q337Q 1011G>A LINC-JP 11 62376116 62376116 single base substitution C T upstream_gene_variant LINC-JP 11 62378437 62378437 single base substitution T C 5_prime_UTR_variant LINC-JP 11 62378437 62378437 single base substitution T C downstream_gene_variant LINC-JP 11 62378437 62378437 single base substitution T C intron_variant LINC-JP 11 62378437 62378437 single base substitution T C synonymous_variant S132S 396A>G LINC-JP 11 62378437 62378437 single base substitution T C synonymous_variant S153S 459A>G LINC-JP 11 62378437 62378437 single base substitution T C synonymous_variant S160S 480A>G LINC-JP 11 62378437 62378437 single base substitution T C synonymous_variant S161S 483A>G LINC-JP 11 62378437 62378437 single base substitution T C upstream_gene_variant LINC-JP 11 62381874 62381874 single base substitution C T upstream_gene_variant LINC-JP 11 62383955 62383955 single base substitution T C upstream_gene_variant LIRI-JP 11 62365859 62365859 single base substitution C T downstream_gene_variant LIRI-JP 11 62366677 62366678 deletion of <=200bp GG - downstream_gene_variant LIRI-JP 11 62373053 62373053 single base substitution G A downstream_gene_variant LIRI-JP 11 62373053 62373053 single base substitution G A intron_variant LIRI-JP 11 62373053 62373053 single base substitution G A upstream_gene_variant LIRI-JP 11 62375549 62375549 single base substitution G A downstream_gene_variant LIRI-JP 11 62375549 62375549 single base substitution G A intron_variant LIRI-JP 11 62375549 62375549 single base substitution G A upstream_gene_variant LIRI-JP 11 62381365 62381367 deletion of <=200bp TCC - upstream_gene_variant LIRI-JP 11 62381722 62381722 single base substitution C A upstream_gene_variant LUSC-KR 11 62364990 62364990 single base substitution G A downstream_gene_variant LUSC-KR 11 62365058 62365058 single base substitution C A downstream_gene_variant LUSC-KR 11 62371139 62371139 single base substitution C T downstream_gene_variant LUSC-KR 11 62371139 62371139 single base substitution C T intron_variant LUSC-KR 11 62374747 62374747 single base substitution C G downstream_gene_variant LUSC-KR 11 62374747 62374747 single base substitution C G exon_variant LUSC-KR 11 62374747 62374747 single base substitution C G intron_variant LUSC-KR 11 62374747 62374747 single base substitution C G upstream_gene_variant LUSC-KR 11 62377433 62377433 single base substitution C G downstream_gene_variant LUSC-KR 11 62377433 62377433 single base substitution C G intron_variant LUSC-KR 11 62377433 62377433 single base substitution C G upstream_gene_variant LUSC-US 11 62371615 62371615 single base substitution C G 3_prime_UTR_variant LUSC-US 11 62371615 62371615 single base substitution C G downstream_gene_variant LUSC-US 11 62371615 62371615 single base substitution C G exon_variant LUSC-US 11 62371615 62371615 single base substitution C G missense_variant E464Q 1390G>C LUSC-US 11 62371615 62371615 single base substitution C G missense_variant E653Q 1957G>C LUSC-US 11 62371615 62371615 single base substitution C G missense_variant E674Q 2020G>C LUSC-US 11 62371615 62371615 single base substitution C G missense_variant E681Q 2041G>C LUSC-US 11 62371615 62371615 single base substitution C G missense_variant E682Q 2044G>C LUSC-US 11 62371615 62371615 single base substitution C G upstream_gene_variant LUSC-US 11 62373335 62373335 single base substitution C T 3_prime_UTR_variant LUSC-US 11 62373335 62373335 single base substitution C T downstream_gene_variant LUSC-US 11 62373335 62373335 single base substitution C T exon_variant LUSC-US 11 62373335 62373335 single base substitution C T missense_variant V375I 1123G>A LUSC-US 11 62373335 62373335 single base substitution C T missense_variant V564I 1690G>A LUSC-US 11 62373335 62373335 single base substitution C T missense_variant V585I 1753G>A LUSC-US 11 62373335 62373335 single base substitution C T missense_variant V592I 1774G>A LUSC-US 11 62373335 62373335 single base substitution C T missense_variant V593I 1777G>A LUSC-US 11 62373335 62373335 single base substitution C T upstream_gene_variant LUSC-US 11 62376917 62376917 single base substitution G A downstream_gene_variant LUSC-US 11 62376917 62376917 single base substitution G A exon_variant LUSC-US 11 62376917 62376917 single base substitution G A missense_variant R195C 583C>T LUSC-US 11 62376917 62376917 single base substitution G A missense_variant R216C 646C>T LUSC-US 11 62376917 62376917 single base substitution G A missense_variant R223C 667C>T LUSC-US 11 62376917 62376917 single base substitution G A missense_variant R224C 670C>T LUSC-US 11 62376917 62376917 single base substitution G A missense_variant R6C 16C>T LUSC-US 11 62376917 62376917 single base substitution G A upstream_gene_variant LUSC-US 11 62378413 62378413 single base substitution C T 5_prime_UTR_variant LUSC-US 11 62378413 62378413 single base substitution C T downstream_gene_variant LUSC-US 11 62378413 62378413 single base substitution C T exon_variant LUSC-US 11 62378413 62378413 single base substitution C T synonymous_variant Q140Q 420G>A LUSC-US 11 62378413 62378413 single base substitution C T synonymous_variant Q161Q 483G>A LUSC-US 11 62378413 62378413 single base substitution C T synonymous_variant Q168Q 504G>A LUSC-US 11 62378413 62378413 single base substitution C T synonymous_variant Q169Q 507G>A LUSC-US 11 62378413 62378413 single base substitution C T upstream_gene_variant LUSC-US 11 62382190 62382190 single base substitution C A upstream_gene_variant MALY-DE 11 62366367 62366367 single base substitution G A downstream_gene_variant MALY-DE 11 62377295 62377295 single base substitution C T downstream_gene_variant MALY-DE 11 62377295 62377295 single base substitution C T intron_variant MALY-DE 11 62377295 62377295 single base substitution C T upstream_gene_variant MALY-DE 11 62383560 62383560 insertion of <=200bp - A upstream_gene_variant MELA-AU 11 62364994 62364994 single base substitution G A downstream_gene_variant MELA-AU 11 62365267 62365267 single base substitution C A downstream_gene_variant MELA-AU 11 62365450 62365450 single base substitution G A downstream_gene_variant MELA-AU 11 62366115 62366115 single base substitution G A downstream_gene_variant MELA-AU 11 62366922 62366922 single base substitution G A downstream_gene_variant MELA-AU 11 62367132 62367132 single base substitution G A downstream_gene_variant MELA-AU 11 62368097 62368097 single base substitution G A downstream_gene_variant MELA-AU 11 62368246 62368246 single base substitution T C downstream_gene_variant MELA-AU 11 62368350 62368350 single base substitution A C downstream_gene_variant MELA-AU 11 62369296 62369296 single base substitution C T downstream_gene_variant MELA-AU 11 62369457 62369457 single base substitution G A downstream_gene_variant MELA-AU 11 62369901 62369901 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62369901 62369901 single base substitution G A downstream_gene_variant MELA-AU 11 62369901 62369901 single base substitution G A exon_variant MELA-AU 11 62369901 62369901 single base substitution G A missense_variant P848L 2543C>T MELA-AU 11 62369901 62369901 single base substitution G A missense_variant P869L 2606C>T MELA-AU 11 62369901 62369901 single base substitution G A missense_variant P876L 2627C>T MELA-AU 11 62369932 62369933 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 11 62369932 62369933 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 62369932 62369933 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 11 62369932 62369933 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant RD837RN MELA-AU 11 62369932 62369933 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant RD858RN MELA-AU 11 62369932 62369933 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant RD865RN MELA-AU 11 62370170 62370170 single base substitution T A downstream_gene_variant MELA-AU 11 62370170 62370170 single base substitution T A intron_variant MELA-AU 11 62370170 62370170 single base substitution T A missense_variant Q64L 191A>T MELA-AU 11 62371281 62371281 single base substitution G T 3_prime_UTR_variant MELA-AU 11 62371281 62371281 single base substitution G T downstream_gene_variant MELA-AU 11 62371281 62371281 single base substitution G T exon_variant MELA-AU 11 62371281 62371281 single base substitution G T missense_variant S509Y 1526C>A MELA-AU 11 62371281 62371281 single base substitution G T missense_variant S698Y 2093C>A MELA-AU 11 62371281 62371281 single base substitution G T missense_variant S719Y 2156C>A MELA-AU 11 62371281 62371281 single base substitution G T missense_variant S726Y 2177C>A MELA-AU 11 62371281 62371281 single base substitution G T missense_variant S727Y 2180C>A MELA-AU 11 62371281 62371281 single base substitution G T upstream_gene_variant MELA-AU 11 62371309 62371309 single base substitution T C downstream_gene_variant MELA-AU 11 62371309 62371309 single base substitution T C intron_variant MELA-AU 11 62371309 62371309 single base substitution T C upstream_gene_variant MELA-AU 11 62371681 62371681 single base substitution G A downstream_gene_variant MELA-AU 11 62371681 62371681 single base substitution G A intron_variant MELA-AU 11 62371681 62371681 single base substitution G A splice_region_variant MELA-AU 11 62371681 62371681 single base substitution G A upstream_gene_variant MELA-AU 11 62372181 62372181 single base substitution G A downstream_gene_variant MELA-AU 11 62372181 62372181 single base substitution G A exon_variant MELA-AU 11 62372181 62372181 single base substitution G A intron_variant MELA-AU 11 62372181 62372181 single base substitution G A upstream_gene_variant MELA-AU 11 62372657 62372657 single base substitution G A downstream_gene_variant MELA-AU 11 62372657 62372657 single base substitution G A exon_variant MELA-AU 11 62372657 62372657 single base substitution G A intron_variant MELA-AU 11 62372657 62372657 single base substitution G A splice_region_variant MELA-AU 11 62372657 62372657 single base substitution G A upstream_gene_variant MELA-AU 11 62372752 62372753 multiple base substitution (>=2bp and <=200bp) GG TA downstream_gene_variant MELA-AU 11 62372752 62372753 multiple base substitution (>=2bp and <=200bp) GG TA intron_variant MELA-AU 11 62372752 62372753 multiple base substitution (>=2bp and <=200bp) GG TA upstream_gene_variant MELA-AU 11 62372886 62372886 single base substitution G A downstream_gene_variant MELA-AU 11 62372886 62372886 single base substitution G A intron_variant MELA-AU 11 62372886 62372886 single base substitution G A upstream_gene_variant MELA-AU 11 62373228 62373228 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62373228 62373228 single base substitution G A downstream_gene_variant MELA-AU 11 62373228 62373228 single base substitution G A exon_variant MELA-AU 11 62373228 62373228 single base substitution G A synonymous_variant L383L 1149C>T MELA-AU 11 62373228 62373228 single base substitution G A synonymous_variant L572L 1716C>T MELA-AU 11 62373228 62373228 single base substitution G A synonymous_variant L593L 1779C>T MELA-AU 11 62373228 62373228 single base substitution G A synonymous_variant L600L 1800C>T MELA-AU 11 62373228 62373228 single base substitution G A synonymous_variant L601L 1803C>T MELA-AU 11 62373228 62373228 single base substitution G A upstream_gene_variant MELA-AU 11 62373338 62373338 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62373338 62373338 single base substitution G A downstream_gene_variant MELA-AU 11 62373338 62373338 single base substitution G A exon_variant MELA-AU 11 62373338 62373338 single base substitution G A missense_variant P374S 1120C>T MELA-AU 11 62373338 62373338 single base substitution G A missense_variant P563S 1687C>T MELA-AU 11 62373338 62373338 single base substitution G A missense_variant P584S 1750C>T MELA-AU 11 62373338 62373338 single base substitution G A missense_variant P591S 1771C>T MELA-AU 11 62373338 62373338 single base substitution G A missense_variant P592S 1774C>T MELA-AU 11 62373338 62373338 single base substitution G A upstream_gene_variant MELA-AU 11 62373566 62373566 single base substitution C A 3_prime_UTR_variant MELA-AU 11 62373566 62373566 single base substitution C A downstream_gene_variant MELA-AU 11 62373566 62373566 single base substitution C A exon_variant MELA-AU 11 62373566 62373566 single base substitution C A missense_variant G325V 974G>T MELA-AU 11 62373566 62373566 single base substitution C A missense_variant G514V 1541G>T MELA-AU 11 62373566 62373566 single base substitution C A missense_variant G535V 1604G>T MELA-AU 11 62373566 62373566 single base substitution C A missense_variant G542V 1625G>T MELA-AU 11 62373566 62373566 single base substitution C A missense_variant G543V 1628G>T MELA-AU 11 62373566 62373566 single base substitution C A upstream_gene_variant MELA-AU 11 62374680 62374680 single base substitution G A downstream_gene_variant MELA-AU 11 62374680 62374680 single base substitution G A exon_variant MELA-AU 11 62374680 62374680 single base substitution G A intron_variant MELA-AU 11 62374680 62374680 single base substitution G A upstream_gene_variant MELA-AU 11 62376755 62376755 single base substitution G A downstream_gene_variant MELA-AU 11 62376755 62376755 single base substitution G A intron_variant MELA-AU 11 62376755 62376755 single base substitution G A upstream_gene_variant MELA-AU 11 62376805 62376805 single base substitution G A downstream_gene_variant MELA-AU 11 62376805 62376805 single base substitution G A intron_variant MELA-AU 11 62376805 62376805 single base substitution G A upstream_gene_variant MELA-AU 11 62376821 62376821 single base substitution G A downstream_gene_variant MELA-AU 11 62376821 62376821 single base substitution G A splice_region_variant MELA-AU 11 62376821 62376821 single base substitution G A upstream_gene_variant MELA-AU 11 62376912 62376912 single base substitution G A downstream_gene_variant MELA-AU 11 62376912 62376912 single base substitution G A exon_variant MELA-AU 11 62376912 62376912 single base substitution G A synonymous_variant P196P 588C>T MELA-AU 11 62376912 62376912 single base substitution G A synonymous_variant P217P 651C>T MELA-AU 11 62376912 62376912 single base substitution G A synonymous_variant P224P 672C>T MELA-AU 11 62376912 62376912 single base substitution G A synonymous_variant P225P 675C>T MELA-AU 11 62376912 62376912 single base substitution G A synonymous_variant P7P 21C>T MELA-AU 11 62376912 62376912 single base substitution G A upstream_gene_variant MELA-AU 11 62376993 62376993 single base substitution G A downstream_gene_variant MELA-AU 11 62376993 62376993 single base substitution G A intron_variant MELA-AU 11 62376993 62376993 single base substitution G A upstream_gene_variant MELA-AU 11 62377151 62377151 single base substitution G A 5_prime_UTR_variant MELA-AU 11 62377151 62377151 single base substitution G A downstream_gene_variant MELA-AU 11 62377151 62377151 single base substitution G A exon_variant MELA-AU 11 62377151 62377151 single base substitution G A missense_variant P167L 500C>T MELA-AU 11 62377151 62377151 single base substitution G A missense_variant P188L 563C>T MELA-AU 11 62377151 62377151 single base substitution G A missense_variant P195L 584C>T MELA-AU 11 62377151 62377151 single base substitution G A missense_variant P196L 587C>T MELA-AU 11 62377151 62377151 single base substitution G A upstream_gene_variant MELA-AU 11 62377194 62377194 single base substitution G A downstream_gene_variant MELA-AU 11 62377194 62377194 single base substitution G A intron_variant MELA-AU 11 62377194 62377194 single base substitution G A upstream_gene_variant MELA-AU 11 62377813 62377813 single base substitution T A downstream_gene_variant MELA-AU 11 62377813 62377813 single base substitution T A intron_variant MELA-AU 11 62377813 62377813 single base substitution T A upstream_gene_variant MELA-AU 11 62378004 62378004 single base substitution G A downstream_gene_variant MELA-AU 11 62378004 62378004 single base substitution G A intron_variant MELA-AU 11 62378004 62378004 single base substitution G A upstream_gene_variant MELA-AU 11 62378026 62378026 single base substitution C G downstream_gene_variant MELA-AU 11 62378026 62378026 single base substitution C G intron_variant MELA-AU 11 62378026 62378026 single base substitution C G upstream_gene_variant MELA-AU 11 62378029 62378029 single base substitution G A downstream_gene_variant MELA-AU 11 62378029 62378029 single base substitution G A intron_variant MELA-AU 11 62378029 62378029 single base substitution G A upstream_gene_variant MELA-AU 11 62378290 62378290 single base substitution G A downstream_gene_variant MELA-AU 11 62378290 62378290 single base substitution G A intron_variant MELA-AU 11 62378290 62378290 single base substitution G A upstream_gene_variant MELA-AU 11 62378625 62378625 single base substitution C T exon_variant MELA-AU 11 62378625 62378625 single base substitution C T missense_variant S100N 299G>A MELA-AU 11 62378625 62378625 single base substitution C T missense_variant S101N 302G>A MELA-AU 11 62378625 62378625 single base substitution C T missense_variant S122N 365G>A MELA-AU 11 62378625 62378625 single base substitution C T missense_variant S129N 386G>A MELA-AU 11 62378625 62378625 single base substitution C T missense_variant S130N 389G>A MELA-AU 11 62378625 62378625 single base substitution C T upstream_gene_variant MELA-AU 11 62378774 62378774 single base substitution G A exon_variant MELA-AU 11 62378774 62378774 single base substitution G A synonymous_variant S50S 150C>T MELA-AU 11 62378774 62378774 single base substitution G A synonymous_variant S51S 153C>T MELA-AU 11 62378774 62378774 single base substitution G A synonymous_variant S72S 216C>T MELA-AU 11 62378774 62378774 single base substitution G A synonymous_variant S79S 237C>T MELA-AU 11 62378774 62378774 single base substitution G A synonymous_variant S80S 240C>T MELA-AU 11 62378774 62378774 single base substitution G A upstream_gene_variant MELA-AU 11 62378876 62378876 single base substitution G A intron_variant MELA-AU 11 62378876 62378876 single base substitution G A upstream_gene_variant MELA-AU 11 62379047 62379047 single base substitution G A 5_prime_UTR_variant MELA-AU 11 62379047 62379047 single base substitution G A missense_variant A15V 44C>T MELA-AU 11 62379047 62379047 single base substitution G A missense_variant A7V 20C>T MELA-AU 11 62379047 62379047 single base substitution G A upstream_gene_variant MELA-AU 11 62380076 62380076 single base substitution G A 5_prime_UTR_variant MELA-AU 11 62380076 62380076 single base substitution G A upstream_gene_variant MELA-AU 11 62380130 62380130 single base substitution C T 5_prime_UTR_variant MELA-AU 11 62380130 62380130 single base substitution C T upstream_gene_variant MELA-AU 11 62380563 62380563 single base substitution G A upstream_gene_variant MELA-AU 11 62380906 62380906 single base substitution C T upstream_gene_variant MELA-AU 11 62381158 62381158 single base substitution G A upstream_gene_variant MELA-AU 11 62382285 62382285 single base substitution C T upstream_gene_variant MELA-AU 11 62382611 62382611 single base substitution G A upstream_gene_variant MELA-AU 11 62382734 62382734 single base substitution C T upstream_gene_variant MELA-AU 11 62383124 62383124 single base substitution C T upstream_gene_variant MELA-AU 11 62383440 62383440 single base substitution G A upstream_gene_variant MELA-AU 11 62383782 62383782 single base substitution G A upstream_gene_variant MELA-AU 11 62384139 62384139 single base substitution G A upstream_gene_variant MELA-AU 11 62384140 62384140 single base substitution G A upstream_gene_variant MELA-AU 11 62384846 62384846 single base substitution A T upstream_gene_variant ORCA-IN 11 62365775 62365775 single base substitution C T downstream_gene_variant ORCA-IN 11 62382150 62382150 single base substitution G A upstream_gene_variant ORCA-IN 11 62384173 62384173 single base substitution G T upstream_gene_variant ORCA-IN 11 62384473 62384473 single base substitution C A upstream_gene_variant OV-AU 11 62365073 62365073 single base substitution A C downstream_gene_variant OV-AU 11 62368959 62368959 single base substitution G T downstream_gene_variant OV-AU 11 62374975 62374975 single base substitution C G downstream_gene_variant OV-AU 11 62374975 62374975 single base substitution C G intron_variant OV-AU 11 62374975 62374975 single base substitution C G upstream_gene_variant OV-AU 11 62378486 62378486 single base substitution T C downstream_gene_variant OV-AU 11 62378486 62378486 single base substitution T C intron_variant OV-AU 11 62378486 62378486 single base substitution T C upstream_gene_variant OV-AU 11 62380533 62380533 single base substitution T C upstream_gene_variant OV-AU 11 62384834 62384834 single base substitution T C upstream_gene_variant OV-US 11 62381310 62381310 single base substitution G A upstream_gene_variant PACA-AU 11 62367489 62367489 deletion of <=200bp A - downstream_gene_variant PACA-AU 11 62368812 62368812 single base substitution C T downstream_gene_variant PACA-AU 11 62371553 62371553 single base substitution G A downstream_gene_variant PACA-AU 11 62371553 62371553 single base substitution G A exon_variant PACA-AU 11 62371553 62371553 single base substitution G A intron_variant PACA-AU 11 62371553 62371553 single base substitution G A upstream_gene_variant PACA-AU 11 62374663 62374663 single base substitution T C downstream_gene_variant PACA-AU 11 62374663 62374663 single base substitution T C exon_variant PACA-AU 11 62374663 62374663 single base substitution T C intron_variant PACA-AU 11 62374663 62374663 single base substitution T C upstream_gene_variant PACA-AU 11 62383376 62383376 single base substitution G A upstream_gene_variant PACA-AU 11 62383442 62383442 single base substitution C T upstream_gene_variant PACA-AU 11 62383717 62383717 single base substitution A C upstream_gene_variant PACA-AU 11 62384468 62384468 single base substitution C G upstream_gene_variant PACA-AU 11 62384510 62384510 single base substitution G A upstream_gene_variant PACA-CA 11 62365581 62365581 single base substitution G A downstream_gene_variant PACA-CA 11 62370804 62370804 single base substitution G A downstream_gene_variant PACA-CA 11 62370804 62370804 single base substitution G A intron_variant PACA-CA 11 62373565 62373565 deletion of <=200bp C - 3_prime_UTR_variant PACA-CA 11 62373565 62373565 deletion of <=200bp C - downstream_gene_variant PACA-CA 11 62373565 62373565 deletion of <=200bp C - exon_variant PACA-CA 11 62373565 62373565 deletion of <=200bp C - frameshift_variant G325 PACA-CA 11 62373565 62373565 deletion of <=200bp C - frameshift_variant G514 PACA-CA 11 62373565 62373565 deletion of <=200bp C - frameshift_variant G535 PACA-CA 11 62373565 62373565 deletion of <=200bp C - frameshift_variant G542 PACA-CA 11 62373565 62373565 deletion of <=200bp C - frameshift_variant G543 PACA-CA 11 62373565 62373565 deletion of <=200bp C - upstream_gene_variant PACA-CA 11 62374189 62374189 single base substitution C T downstream_gene_variant PACA-CA 11 62374189 62374189 single base substitution C T intron_variant PACA-CA 11 62374189 62374189 single base substitution C T upstream_gene_variant PACA-CA 11 62378364 62378364 single base substitution C T 5_prime_UTR_variant PACA-CA 11 62378364 62378364 single base substitution C T downstream_gene_variant PACA-CA 11 62378364 62378364 single base substitution C T exon_variant PACA-CA 11 62378364 62378364 single base substitution C T missense_variant G157R 469G>A PACA-CA 11 62378364 62378364 single base substitution C T missense_variant G178R 532G>A PACA-CA 11 62378364 62378364 single base substitution C T missense_variant G185R 553G>A PACA-CA 11 62378364 62378364 single base substitution C T missense_variant G186R 556G>A PACA-CA 11 62378364 62378364 single base substitution C T upstream_gene_variant PACA-CA 11 62380733 62380733 single base substitution T C upstream_gene_variant PACA-CA 11 62381703 62381703 insertion of <=200bp - T upstream_gene_variant PACA-CA 11 62384144 62384144 single base substitution G A upstream_gene_variant PAEN-AU 11 62364909 62364909 single base substitution C T downstream_gene_variant PAEN-AU 11 62373211 62373211 single base substitution T G 3_prime_UTR_variant PAEN-AU 11 62373211 62373211 single base substitution T G downstream_gene_variant PAEN-AU 11 62373211 62373211 single base substitution T G exon_variant PAEN-AU 11 62373211 62373211 single base substitution T G missense_variant H389P 1166A>C PAEN-AU 11 62373211 62373211 single base substitution T G missense_variant H578P 1733A>C PAEN-AU 11 62373211 62373211 single base substitution T G missense_variant H599P 1796A>C PAEN-AU 11 62373211 62373211 single base substitution T G missense_variant H606P 1817A>C PAEN-AU 11 62373211 62373211 single base substitution T G missense_variant H607P 1820A>C PAEN-AU 11 62373211 62373211 single base substitution T G upstream_gene_variant PAEN-IT 11 62379742 62379742 single base substitution C A 5_prime_UTR_variant PAEN-IT 11 62379742 62379742 single base substitution C A intron_variant PAEN-IT 11 62379742 62379742 single base substitution C A upstream_gene_variant PBCA-DE 11 62369277 62369277 single base substitution C T downstream_gene_variant PBCA-DE 11 62374928 62374928 single base substitution G A downstream_gene_variant PBCA-DE 11 62374928 62374928 single base substitution G A intron_variant PBCA-DE 11 62374928 62374928 single base substitution G A upstream_gene_variant PBCA-DE 11 62375645 62375645 single base substitution G T downstream_gene_variant PBCA-DE 11 62375645 62375645 single base substitution G T intron_variant PBCA-DE 11 62375645 62375645 single base substitution G T upstream_gene_variant PRAD-UK 11 62369783 62369783 single base substitution G A 3_prime_UTR_variant PRAD-UK 11 62369783 62369783 single base substitution G A downstream_gene_variant PRAD-UK 11 62369783 62369783 single base substitution G A exon_variant PRAD-UK 11 62369783 62369783 single base substitution G A synonymous_variant H887H 2661C>T PRAD-UK 11 62369783 62369783 single base substitution G A synonymous_variant H908H 2724C>T PRAD-UK 11 62369783 62369783 single base substitution G A synonymous_variant H915H 2745C>T PRAD-US 11 62378665 62378665 single base substitution G A exon_variant PRAD-US 11 62378665 62378665 single base substitution G A missense_variant P109S 325C>T PRAD-US 11 62378665 62378665 single base substitution G A missense_variant P116S 346C>T PRAD-US 11 62378665 62378665 single base substitution G A missense_variant P117S 349C>T PRAD-US 11 62378665 62378665 single base substitution G A missense_variant P87S 259C>T PRAD-US 11 62378665 62378665 single base substitution G A missense_variant P88S 262C>T PRAD-US 11 62378665 62378665 single base substitution G A upstream_gene_variant PRAD-US 11 62384117 62384117 single base substitution G A upstream_gene_variant READ-US 11 62373378 62373378 single base substitution C A 3_prime_UTR_variant READ-US 11 62373378 62373378 single base substitution C A downstream_gene_variant READ-US 11 62373378 62373378 single base substitution C A exon_variant READ-US 11 62373378 62373378 single base substitution C A missense_variant K360N 1080G>T READ-US 11 62373378 62373378 single base substitution C A missense_variant K549N 1647G>T READ-US 11 62373378 62373378 single base substitution C A missense_variant K570N 1710G>T READ-US 11 62373378 62373378 single base substitution C A missense_variant K577N 1731G>T READ-US 11 62373378 62373378 single base substitution C A missense_variant K578N 1734G>T READ-US 11 62373378 62373378 single base substitution C A upstream_gene_variant READ-US 11 62381856 62381856 single base substitution C T upstream_gene_variant RECA-EU 11 62372275 62372275 single base substitution C G downstream_gene_variant RECA-EU 11 62372275 62372275 single base substitution C G exon_variant RECA-EU 11 62372275 62372275 single base substitution C G intron_variant RECA-EU 11 62372275 62372275 single base substitution C G upstream_gene_variant RECA-EU 11 62384535 62384535 single base substitution G T upstream_gene_variant RECA-EU 11 62384784 62384784 single base substitution T A upstream_gene_variant SKCA-BR 11 62366901 62366901 single base substitution A G downstream_gene_variant SKCA-BR 11 62369211 62369211 single base substitution A C downstream_gene_variant SKCA-BR 11 62369264 62369264 single base substitution A G downstream_gene_variant SKCA-BR 11 62380518 62380518 single base substitution T G upstream_gene_variant SKCA-BR 11 62381483 62381483 single base substitution T C upstream_gene_variant SKCA-BR 11 62384104 62384104 single base substitution G A upstream_gene_variant SKCA-BR 11 62384105 62384105 single base substitution G A upstream_gene_variant SKCA-BR 11 62384296 62384296 single base substitution G A upstream_gene_variant SKCM-US 11 62365529 62365529 single base substitution A G downstream_gene_variant SKCM-US 11 62367695 62367695 single base substitution G A downstream_gene_variant SKCM-US 11 62368097 62368097 single base substitution G A downstream_gene_variant SKCM-US 11 62372641 62372641 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62372641 62372641 single base substitution G A downstream_gene_variant SKCM-US 11 62372641 62372641 single base substitution G A exon_variant SKCM-US 11 62372641 62372641 single base substitution G A synonymous_variant L425L 1275C>T SKCM-US 11 62372641 62372641 single base substitution G A synonymous_variant L614L 1842C>T SKCM-US 11 62372641 62372641 single base substitution G A synonymous_variant L635L 1905C>T SKCM-US 11 62372641 62372641 single base substitution G A synonymous_variant L642L 1926C>T SKCM-US 11 62372641 62372641 single base substitution G A synonymous_variant L643L 1929C>T SKCM-US 11 62372641 62372641 single base substitution G A upstream_gene_variant SKCM-US 11 62373192 62373192 single base substitution G T 3_prime_UTR_variant SKCM-US 11 62373192 62373192 single base substitution G T downstream_gene_variant SKCM-US 11 62373192 62373192 single base substitution G T exon_variant SKCM-US 11 62373192 62373192 single base substitution G T missense_variant F395L 1185C>A SKCM-US 11 62373192 62373192 single base substitution G T missense_variant F584L 1752C>A SKCM-US 11 62373192 62373192 single base substitution G T missense_variant F605L 1815C>A SKCM-US 11 62373192 62373192 single base substitution G T missense_variant F612L 1836C>A SKCM-US 11 62373192 62373192 single base substitution G T missense_variant F613L 1839C>A SKCM-US 11 62373192 62373192 single base substitution G T upstream_gene_variant SKCM-US 11 62373339 62373339 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62373339 62373339 single base substitution G A downstream_gene_variant SKCM-US 11 62373339 62373339 single base substitution G A exon_variant SKCM-US 11 62373339 62373339 single base substitution G A synonymous_variant S373S 1119C>T SKCM-US 11 62373339 62373339 single base substitution G A synonymous_variant S562S 1686C>T SKCM-US 11 62373339 62373339 single base substitution G A synonymous_variant S583S 1749C>T SKCM-US 11 62373339 62373339 single base substitution G A synonymous_variant S590S 1770C>T SKCM-US 11 62373339 62373339 single base substitution G A synonymous_variant S591S 1773C>T SKCM-US 11 62373339 62373339 single base substitution G A upstream_gene_variant SKCM-US 11 62373563 62373563 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62373563 62373563 single base substitution G A downstream_gene_variant SKCM-US 11 62373563 62373563 single base substitution G A exon_variant SKCM-US 11 62373563 62373563 single base substitution G A missense_variant P326L 977C>T SKCM-US 11 62373563 62373563 single base substitution G A missense_variant P515L 1544C>T SKCM-US 11 62373563 62373563 single base substitution G A missense_variant P536L 1607C>T SKCM-US 11 62373563 62373563 single base substitution G A missense_variant P543L 1628C>T SKCM-US 11 62373563 62373563 single base substitution G A missense_variant P544L 1631C>T SKCM-US 11 62373563 62373563 single base substitution G A upstream_gene_variant SKCM-US 11 62373585 62373585 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62373585 62373585 single base substitution G A downstream_gene_variant SKCM-US 11 62373585 62373585 single base substitution G A exon_variant SKCM-US 11 62373585 62373585 single base substitution G A missense_variant R319C 955C>T SKCM-US 11 62373585 62373585 single base substitution G A missense_variant R508C 1522C>T SKCM-US 11 62373585 62373585 single base substitution G A missense_variant R529C 1585C>T SKCM-US 11 62373585 62373585 single base substitution G A missense_variant R536C 1606C>T SKCM-US 11 62373585 62373585 single base substitution G A missense_variant R537C 1609C>T SKCM-US 11 62373585 62373585 single base substitution G A upstream_gene_variant SKCM-US 11 62373637 62373637 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62373637 62373637 single base substitution G A downstream_gene_variant SKCM-US 11 62373637 62373637 single base substitution G A exon_variant SKCM-US 11 62373637 62373637 single base substitution G A synonymous_variant F301F 903C>T SKCM-US 11 62373637 62373637 single base substitution G A synonymous_variant F490F 1470C>T SKCM-US 11 62373637 62373637 single base substitution G A synonymous_variant F511F 1533C>T SKCM-US 11 62373637 62373637 single base substitution G A synonymous_variant F518F 1554C>T SKCM-US 11 62373637 62373637 single base substitution G A synonymous_variant F519F 1557C>T SKCM-US 11 62373637 62373637 single base substitution G A upstream_gene_variant SKCM-US 11 62375207 62375207 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62375207 62375207 single base substitution G A downstream_gene_variant SKCM-US 11 62375207 62375207 single base substitution G A intron_variant SKCM-US 11 62375207 62375207 single base substitution G A synonymous_variant F214F 642C>T SKCM-US 11 62375207 62375207 single base substitution G A synonymous_variant F403F 1209C>T SKCM-US 11 62375207 62375207 single base substitution G A synonymous_variant F424F 1272C>T SKCM-US 11 62375207 62375207 single base substitution G A synonymous_variant F431F 1293C>T SKCM-US 11 62375207 62375207 single base substitution G A synonymous_variant F432F 1296C>T SKCM-US 11 62375207 62375207 single base substitution G A upstream_gene_variant SKCM-US 11 62375218 62375218 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62375218 62375218 single base substitution G A downstream_gene_variant SKCM-US 11 62375218 62375218 single base substitution G A intron_variant SKCM-US 11 62375218 62375218 single base substitution G A missense_variant H211Y 631C>T SKCM-US 11 62375218 62375218 single base substitution G A missense_variant H400Y 1198C>T SKCM-US 11 62375218 62375218 single base substitution G A missense_variant H421Y 1261C>T SKCM-US 11 62375218 62375218 single base substitution G A missense_variant H428Y 1282C>T SKCM-US 11 62375218 62375218 single base substitution G A missense_variant H429Y 1285C>T SKCM-US 11 62375218 62375218 single base substitution G A upstream_gene_variant SKCM-US 11 62375742 62375742 single base substitution C A 3_prime_UTR_variant SKCM-US 11 62375742 62375742 single base substitution C A downstream_gene_variant SKCM-US 11 62375742 62375742 single base substitution C A synonymous_variant V162V 486G>T SKCM-US 11 62375742 62375742 single base substitution C A synonymous_variant V351V 1053G>T SKCM-US 11 62375742 62375742 single base substitution C A synonymous_variant V372V 1116G>T SKCM-US 11 62375742 62375742 single base substitution C A synonymous_variant V379V 1137G>T SKCM-US 11 62375742 62375742 single base substitution C A synonymous_variant V380V 1140G>T SKCM-US 11 62375742 62375742 single base substitution C A upstream_gene_variant SKCM-US 11 62376026 62376026 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62376026 62376026 single base substitution G A downstream_gene_variant SKCM-US 11 62376026 62376026 single base substitution G A synonymous_variant A149A 447C>T SKCM-US 11 62376026 62376026 single base substitution G A synonymous_variant A338A 1014C>T SKCM-US 11 62376026 62376026 single base substitution G A synonymous_variant A359A 1077C>T SKCM-US 11 62376026 62376026 single base substitution G A synonymous_variant A366A 1098C>T SKCM-US 11 62376026 62376026 single base substitution G A synonymous_variant A367A 1101C>T SKCM-US 11 62376026 62376026 single base substitution G A upstream_gene_variant SKCM-US 11 62376050 62376050 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62376050 62376050 single base substitution G A downstream_gene_variant SKCM-US 11 62376050 62376050 single base substitution G A synonymous_variant F141F 423C>T SKCM-US 11 62376050 62376050 single base substitution G A synonymous_variant F330F 990C>T SKCM-US 11 62376050 62376050 single base substitution G A synonymous_variant F351F 1053C>T SKCM-US 11 62376050 62376050 single base substitution G A synonymous_variant F358F 1074C>T SKCM-US 11 62376050 62376050 single base substitution G A synonymous_variant F359F 1077C>T SKCM-US 11 62376050 62376050 single base substitution G A upstream_gene_variant SKCM-US 11 62376529 62376529 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62376529 62376529 single base substitution G A downstream_gene_variant SKCM-US 11 62376529 62376529 single base substitution G A synonymous_variant A250A 750C>T SKCM-US 11 62376529 62376529 single base substitution G A synonymous_variant A271A 813C>T SKCM-US 11 62376529 62376529 single base substitution G A synonymous_variant A278A 834C>T SKCM-US 11 62376529 62376529 single base substitution G A synonymous_variant A279A 837C>T SKCM-US 11 62376529 62376529 single base substitution G A synonymous_variant A61A 183C>T SKCM-US 11 62376529 62376529 single base substitution G A upstream_gene_variant SKCM-US 11 62376896 62376896 single base substitution G A downstream_gene_variant SKCM-US 11 62376896 62376896 single base substitution G A exon_variant SKCM-US 11 62376896 62376896 single base substitution G A missense_variant P13S 37C>T SKCM-US 11 62376896 62376896 single base substitution G A missense_variant P202S 604C>T SKCM-US 11 62376896 62376896 single base substitution G A missense_variant P223S 667C>T SKCM-US 11 62376896 62376896 single base substitution G A missense_variant P230S 688C>T SKCM-US 11 62376896 62376896 single base substitution G A missense_variant P231S 691C>T SKCM-US 11 62376896 62376896 single base substitution G A upstream_gene_variant SKCM-US 11 62376927 62376927 single base substitution G A downstream_gene_variant SKCM-US 11 62376927 62376927 single base substitution G A exon_variant SKCM-US 11 62376927 62376927 single base substitution G A synonymous_variant F191F 573C>T SKCM-US 11 62376927 62376927 single base substitution G A synonymous_variant F212F 636C>T SKCM-US 11 62376927 62376927 single base substitution G A synonymous_variant F219F 657C>T SKCM-US 11 62376927 62376927 single base substitution G A synonymous_variant F220F 660C>T SKCM-US 11 62376927 62376927 single base substitution G A synonymous_variant F2F 6C>T SKCM-US 11 62376927 62376927 single base substitution G A upstream_gene_variant SKCM-US 11 62377144 62377144 single base substitution G A 5_prime_UTR_variant SKCM-US 11 62377144 62377144 single base substitution G A downstream_gene_variant SKCM-US 11 62377144 62377144 single base substitution G A exon_variant SKCM-US 11 62377144 62377144 single base substitution G A synonymous_variant S169S 507C>T SKCM-US 11 62377144 62377144 single base substitution G A synonymous_variant S190S 570C>T SKCM-US 11 62377144 62377144 single base substitution G A synonymous_variant S197S 591C>T SKCM-US 11 62377144 62377144 single base substitution G A synonymous_variant S198S 594C>T SKCM-US 11 62377144 62377144 single base substitution G A upstream_gene_variant SKCM-US 11 62378444 62378444 single base substitution G A 5_prime_UTR_variant SKCM-US 11 62378444 62378444 single base substitution G A downstream_gene_variant SKCM-US 11 62378444 62378444 single base substitution G A intron_variant SKCM-US 11 62378444 62378444 single base substitution G A missense_variant S130F 389C>T SKCM-US 11 62378444 62378444 single base substitution G A missense_variant S151F 452C>T SKCM-US 11 62378444 62378444 single base substitution G A missense_variant S158F 473C>T SKCM-US 11 62378444 62378444 single base substitution G A missense_variant S159F 476C>T SKCM-US 11 62378444 62378444 single base substitution G A upstream_gene_variant SKCM-US 11 62378686 62378686 single base substitution G A exon_variant SKCM-US 11 62378686 62378686 single base substitution G A missense_variant P102S 304C>T SKCM-US 11 62378686 62378686 single base substitution G A missense_variant P109S 325C>T SKCM-US 11 62378686 62378686 single base substitution G A missense_variant P110S 328C>T SKCM-US 11 62378686 62378686 single base substitution G A missense_variant P80S 238C>T SKCM-US 11 62378686 62378686 single base substitution G A missense_variant P81S 241C>T SKCM-US 11 62378686 62378686 single base substitution G A upstream_gene_variant SKCM-US 11 62378723 62378723 single base substitution G A exon_variant SKCM-US 11 62378723 62378723 single base substitution G A synonymous_variant S67S 201C>T SKCM-US 11 62378723 62378723 single base substitution G A synonymous_variant S68S 204C>T SKCM-US 11 62378723 62378723 single base substitution G A synonymous_variant S89S 267C>T SKCM-US 11 62378723 62378723 single base substitution G A synonymous_variant S96S 288C>T SKCM-US 11 62378723 62378723 single base substitution G A synonymous_variant S97S 291C>T SKCM-US 11 62378723 62378723 single base substitution G A upstream_gene_variant SKCM-US 11 62380861 62380861 single base substitution C A upstream_gene_variant SKCM-US 11 62381081 62381081 single base substitution G A upstream_gene_variant SKCM-US 11 62382274 62382274 single base substitution G A upstream_gene_variant SKCM-US 11 62383255 62383255 single base substitution G A upstream_gene_variant SKCM-US 11 62384058 62384058 single base substitution G A upstream_gene_variant SKCM-US 11 62384058 62384058 single base substitution G C upstream_gene_variant SKCM-US 11 62384138 62384138 single base substitution G A upstream_gene_variant SKCM-US 11 62384617 62384617 single base substitution G A upstream_gene_variant STAD-US 11 62365105 62365105 single base substitution G A downstream_gene_variant STAD-US 11 62365601 62365601 deletion of <=200bp A - downstream_gene_variant STAD-US 11 62374527 62374527 single base substitution C T 3_prime_UTR_variant STAD-US 11 62374527 62374527 single base substitution C T downstream_gene_variant STAD-US 11 62374527 62374527 single base substitution C T exon_variant STAD-US 11 62374527 62374527 single base substitution C T synonymous_variant P252P 756G>A STAD-US 11 62374527 62374527 single base substitution C T synonymous_variant P441P 1323G>A STAD-US 11 62374527 62374527 single base substitution C T synonymous_variant P462P 1386G>A STAD-US 11 62374527 62374527 single base substitution C T synonymous_variant P469P 1407G>A STAD-US 11 62374527 62374527 single base substitution C T synonymous_variant P470P 1410G>A STAD-US 11 62374527 62374527 single base substitution C T upstream_gene_variant STAD-US 11 62375291 62375291 single base substitution A G downstream_gene_variant STAD-US 11 62375291 62375291 single base substitution A G intron_variant STAD-US 11 62375291 62375291 single base substitution A G splice_region_variant STAD-US 11 62375291 62375291 single base substitution A G upstream_gene_variant STAD-US 11 62376074 62376074 single base substitution C T 3_prime_UTR_variant STAD-US 11 62376074 62376074 single base substitution C T downstream_gene_variant STAD-US 11 62376074 62376074 single base substitution C T synonymous_variant L133L 399G>A STAD-US 11 62376074 62376074 single base substitution C T synonymous_variant L322L 966G>A STAD-US 11 62376074 62376074 single base substitution C T synonymous_variant L343L 1029G>A STAD-US 11 62376074 62376074 single base substitution C T synonymous_variant L350L 1050G>A STAD-US 11 62376074 62376074 single base substitution C T synonymous_variant L351L 1053G>A STAD-US 11 62376074 62376074 single base substitution C T upstream_gene_variant STAD-US 11 62376111 62376111 single base substitution A G 3_prime_UTR_variant STAD-US 11 62376111 62376111 single base substitution A G downstream_gene_variant STAD-US 11 62376111 62376111 single base substitution A G missense_variant V121A 362T>C STAD-US 11 62376111 62376111 single base substitution A G missense_variant V310A 929T>C STAD-US 11 62376111 62376111 single base substitution A G missense_variant V331A 992T>C STAD-US 11 62376111 62376111 single base substitution A G missense_variant V338A 1013T>C STAD-US 11 62376111 62376111 single base substitution A G missense_variant V339A 1016T>C STAD-US 11 62376111 62376111 single base substitution A G upstream_gene_variant STAD-US 11 62376557 62376557 single base substitution C T 3_prime_UTR_variant STAD-US 11 62376557 62376557 single base substitution C T downstream_gene_variant STAD-US 11 62376557 62376557 single base substitution C T missense_variant R241H 722G>A STAD-US 11 62376557 62376557 single base substitution C T missense_variant R262H 785G>A STAD-US 11 62376557 62376557 single base substitution C T missense_variant R269H 806G>A STAD-US 11 62376557 62376557 single base substitution C T missense_variant R270H 809G>A STAD-US 11 62376557 62376557 single base substitution C T missense_variant R52H 155G>A STAD-US 11 62376557 62376557 single base substitution C T upstream_gene_variant STAD-US 11 62376578 62376578 single base substitution C T 3_prime_UTR_variant STAD-US 11 62376578 62376578 single base substitution C T downstream_gene_variant STAD-US 11 62376578 62376578 single base substitution C T missense_variant R234H 701G>A STAD-US 11 62376578 62376578 single base substitution C T missense_variant R255H 764G>A STAD-US 11 62376578 62376578 single base substitution C T missense_variant R262H 785G>A STAD-US 11 62376578 62376578 single base substitution C T missense_variant R263H 788G>A STAD-US 11 62376578 62376578 single base substitution C T missense_variant R45H 134G>A STAD-US 11 62376578 62376578 single base substitution C T upstream_gene_variant STAD-US 11 62376884 62376884 single base substitution G A downstream_gene_variant STAD-US 11 62376884 62376884 single base substitution G A exon_variant STAD-US 11 62376884 62376884 single base substitution G A missense_variant R17C 49C>T STAD-US 11 62376884 62376884 single base substitution G A missense_variant R206C 616C>T STAD-US 11 62376884 62376884 single base substitution G A missense_variant R227C 679C>T STAD-US 11 62376884 62376884 single base substitution G A missense_variant R234C 700C>T STAD-US 11 62376884 62376884 single base substitution G A missense_variant R235C 703C>T STAD-US 11 62376884 62376884 single base substitution G A upstream_gene_variant STAD-US 11 62377121 62377121 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 62377121 62377121 single base substitution C A downstream_gene_variant STAD-US 11 62377121 62377121 single base substitution C A exon_variant STAD-US 11 62377121 62377121 single base substitution C A missense_variant R177L 530G>T STAD-US 11 62377121 62377121 single base substitution C A missense_variant R198L 593G>T STAD-US 11 62377121 62377121 single base substitution C A missense_variant R205L 614G>T STAD-US 11 62377121 62377121 single base substitution C A missense_variant R206L 617G>T STAD-US 11 62377121 62377121 single base substitution C A upstream_gene_variant STAD-US 11 62377133 62377133 deletion of <=200bp C - 5_prime_UTR_variant STAD-US 11 62377133 62377133 deletion of <=200bp C - downstream_gene_variant STAD-US 11 62377133 62377133 deletion of <=200bp C - exon_variant STAD-US 11 62377133 62377133 deletion of <=200bp C - frameshift_variant G173 STAD-US 11 62377133 62377133 deletion of <=200bp C - frameshift_variant G194 STAD-US 11 62377133 62377133 deletion of <=200bp C - frameshift_variant G201 STAD-US 11 62377133 62377133 deletion of <=200bp C - frameshift_variant G202 STAD-US 11 62377133 62377133 deletion of <=200bp C - upstream_gene_variant STAD-US 11 62378607 62378607 single base substitution C T exon_variant STAD-US 11 62378607 62378607 single base substitution C T missense_variant G106D 317G>A STAD-US 11 62378607 62378607 single base substitution C T missense_variant G107D 320G>A STAD-US 11 62378607 62378607 single base substitution C T missense_variant G128D 383G>A STAD-US 11 62378607 62378607 single base substitution C T missense_variant G135D 404G>A STAD-US 11 62378607 62378607 single base substitution C T missense_variant G136D 407G>A STAD-US 11 62378607 62378607 single base substitution C T upstream_gene_variant STAD-US 11 62378802 62378802 deletion of <=200bp G - exon_variant STAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P41 STAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P42 STAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P63 STAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P70 STAD-US 11 62378802 62378802 deletion of <=200bp G - frameshift_variant P71 STAD-US 11 62378802 62378802 deletion of <=200bp G - upstream_gene_variant STAD-US 11 62378802 62378802 insertion of <=200bp - G exon_variant STAD-US 11 62378802 62378802 insertion of <=200bp - G frameshift_variant P41P? STAD-US 11 62378802 62378802 insertion of <=200bp - G frameshift_variant P42P? STAD-US 11 62378802 62378802 insertion of <=200bp - G frameshift_variant P63P? STAD-US 11 62378802 62378802 insertion of <=200bp - G frameshift_variant P70P? STAD-US 11 62378802 62378802 insertion of <=200bp - G frameshift_variant P71P? STAD-US 11 62378802 62378802 insertion of <=200bp - G upstream_gene_variant STAD-US 11 62380758 62380758 single base substitution C T upstream_gene_variant STAD-US 11 62381147 62381147 single base substitution G A upstream_gene_variant STAD-US 11 62381298 62381298 single base substitution G T upstream_gene_variant STAD-US 11 62381819 62381819 deletion of <=200bp A - upstream_gene_variant STAD-US 11 62381962 62381962 single base substitution A G upstream_gene_variant STAD-US 11 62382265 62382265 deletion of <=200bp C - upstream_gene_variant STAD-US 11 62383980 62383980 single base substitution G A upstream_gene_variant STAD-US 11 62384793 62384793 single base substitution C T upstream_gene_variant STAD-US 11 62384806 62384806 single base substitution C T upstream_gene_variant UCEC-US 11 62366046 62366046 single base substitution G T downstream_gene_variant UCEC-US 11 62370660 62370660 single base substitution A C 3_prime_UTR_variant UCEC-US 11 62370660 62370660 single base substitution A C downstream_gene_variant UCEC-US 11 62370660 62370660 single base substitution A C exon_variant UCEC-US 11 62370660 62370660 single base substitution A C missense_variant W24G 70T>G UCEC-US 11 62370660 62370660 single base substitution A C missense_variant W556G 1666T>G UCEC-US 11 62370660 62370660 single base substitution A C missense_variant W745G 2233T>G UCEC-US 11 62370660 62370660 single base substitution A C missense_variant W766G 2296T>G UCEC-US 11 62370660 62370660 single base substitution A C missense_variant W773G 2317T>G UCEC-US 11 62370660 62370660 single base substitution A C missense_variant W774G 2320T>G UCEC-US 11 62370707 62370707 single base substitution C T 3_prime_UTR_variant UCEC-US 11 62370707 62370707 single base substitution C T downstream_gene_variant UCEC-US 11 62370707 62370707 single base substitution C T exon_variant UCEC-US 11 62370707 62370707 single base substitution C T missense_variant G540E 1619G>A UCEC-US 11 62370707 62370707 single base substitution C T missense_variant G729E 2186G>A UCEC-US 11 62370707 62370707 single base substitution C T missense_variant G750E 2249G>A UCEC-US 11 62370707 62370707 single base substitution C T missense_variant G757E 2270G>A UCEC-US 11 62370707 62370707 single base substitution C T missense_variant G758E 2273G>A UCEC-US 11 62370707 62370707 single base substitution C T missense_variant G8E 23G>A UCEC-US 11 62371266 62371266 single base substitution T C 3_prime_UTR_variant UCEC-US 11 62371266 62371266 single base substitution T C downstream_gene_variant UCEC-US 11 62371266 62371266 single base substitution T C exon_variant UCEC-US 11 62371266 62371266 single base substitution T C missense_variant H514R 1541A>G UCEC-US 11 62371266 62371266 single base substitution T C missense_variant H703R 2108A>G UCEC-US 11 62371266 62371266 single base substitution T C missense_variant H724R 2171A>G UCEC-US 11 62371266 62371266 single base substitution T C missense_variant H731R 2192A>G UCEC-US 11 62371266 62371266 single base substitution T C missense_variant H732R 2195A>G UCEC-US 11 62371266 62371266 single base substitution T C upstream_gene_variant UCEC-US 11 62371473 62371473 single base substitution G A 3_prime_UTR_variant UCEC-US 11 62371473 62371473 single base substitution G A downstream_gene_variant UCEC-US 11 62371473 62371473 single base substitution G A exon_variant UCEC-US 11 62371473 62371473 single base substitution G A synonymous_variant I487I 1461C>T UCEC-US 11 62371473 62371473 single base substitution G A synonymous_variant I676I 2028C>T UCEC-US 11 62371473 62371473 single base substitution G A synonymous_variant I697I 2091C>T UCEC-US 11 62371473 62371473 single base substitution G A synonymous_variant I704I 2112C>T UCEC-US 11 62371473 62371473 single base substitution G A synonymous_variant I705I 2115C>T UCEC-US 11 62371473 62371473 single base substitution G A upstream_gene_variant UCEC-US 11 62373584 62373584 single base substitution C T 3_prime_UTR_variant UCEC-US 11 62373584 62373584 single base substitution C T downstream_gene_variant UCEC-US 11 62373584 62373584 single base substitution C T exon_variant UCEC-US 11 62373584 62373584 single base substitution C T missense_variant R319H 956G>A UCEC-US 11 62373584 62373584 single base substitution C T missense_variant R508H 1523G>A UCEC-US 11 62373584 62373584 single base substitution C T missense_variant R529H 1586G>A UCEC-US 11 62373584 62373584 single base substitution C T missense_variant R536H 1607G>A UCEC-US 11 62373584 62373584 single base substitution C T missense_variant R537H 1610G>A UCEC-US 11 62373584 62373584 single base substitution C T upstream_gene_variant UCEC-US 11 62374518 62374518 single base substitution G A 3_prime_UTR_variant UCEC-US 11 62374518 62374518 single base substitution G A downstream_gene_variant UCEC-US 11 62374518 62374518 single base substitution G A exon_variant UCEC-US 11 62374518 62374518 single base substitution G A synonymous_variant D255D 765C>T UCEC-US 11 62374518 62374518 single base substitution G A synonymous_variant D444D 1332C>T UCEC-US 11 62374518 62374518 single base substitution G A synonymous_variant D465D 1395C>T UCEC-US 11 62374518 62374518 single base substitution G A synonymous_variant D472D 1416C>T UCEC-US 11 62374518 62374518 single base substitution G A synonymous_variant D473D 1419C>T UCEC-US 11 62374518 62374518 single base substitution G A upstream_gene_variant UCEC-US 11 62375716 62375716 single base substitution G A 3_prime_UTR_variant UCEC-US 11 62375716 62375716 single base substitution G A downstream_gene_variant UCEC-US 11 62375716 62375716 single base substitution G A missense_variant S171L 512C>T UCEC-US 11 62375716 62375716 single base substitution G A missense_variant S360L 1079C>T UCEC-US 11 62375716 62375716 single base substitution G A missense_variant S381L 1142C>T UCEC-US 11 62375716 62375716 single base substitution G A missense_variant S388L 1163C>T UCEC-US 11 62375716 62375716 single base substitution G A missense_variant S389L 1166C>T UCEC-US 11 62375716 62375716 single base substitution G A upstream_gene_variant UCEC-US 11 62376884 62376884 single base substitution G A downstream_gene_variant UCEC-US 11 62376884 62376884 single base substitution G A exon_variant UCEC-US 11 62376884 62376884 single base substitution G A missense_variant R17C 49C>T UCEC-US 11 62376884 62376884 single base substitution G A missense_variant R206C 616C>T UCEC-US 11 62376884 62376884 single base substitution G A missense_variant R227C 679C>T UCEC-US 11 62376884 62376884 single base substitution G A missense_variant R234C 700C>T UCEC-US 11 62376884 62376884 single base substitution G A missense_variant R235C 703C>T UCEC-US 11 62376884 62376884 single base substitution G A upstream_gene_variant UCEC-US 11 62378369 62378369 single base substitution C T 5_prime_UTR_variant UCEC-US 11 62378369 62378369 single base substitution C T downstream_gene_variant UCEC-US 11 62378369 62378369 single base substitution C T exon_variant UCEC-US 11 62378369 62378369 single base substitution C T missense_variant R155Q 464G>A UCEC-US 11 62378369 62378369 single base substitution C T missense_variant R176Q 527G>A UCEC-US 11 62378369 62378369 single base substitution C T missense_variant R183Q 548G>A UCEC-US 11 62378369 62378369 single base substitution C T missense_variant R184Q 551G>A UCEC-US 11 62378369 62378369 single base substitution C T upstream_gene_variant UCEC-US 11 62378920 62378920 single base substitution G A exon_variant UCEC-US 11 62378920 62378920 single base substitution G A synonymous_variant G28G 84C>T UCEC-US 11 62378920 62378920 single base substitution G A synonymous_variant G49G 147C>T UCEC-US 11 62378920 62378920 single base substitution G A synonymous_variant G57G 171C>T UCEC-US 11 62378920 62378920 single base substitution G A upstream_gene_variant UCEC-US 11 62381191 62381191 single base substitution C T upstream_gene_variant UCEC-US 11 62381197 62381197 single base substitution G T upstream_gene_variant UCEC-US 11 62381260 62381260 single base substitution C T upstream_gene_variant UCEC-US 11 62381290 62381290 single base substitution G A upstream_gene_variant UCEC-US 11 62382116 62382116 single base substitution G A upstream_gene_variant UCEC-US 11 62382204 62382204 single base substitution G T upstream_gene_variant UCEC-US 11 62384485 62384485 single base substitution T C upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-EE-A3J4-06 COSM3869753 c.1770C>T p.S590S Substitution - coding silent 11:62605867-62605867 - Patient_4 COSM5414439 c.2375C>T p.S792F Substitution - Missense 11:62602871-62602871 - ESCC_BICR_018T COSM5429041 c.1464C>T p.S488S Substitution - coding silent 11:62606998-62606998 - PD9755a COSM5782698 c.692C>T p.S231F Substitution - Missense 11:62609420-62609420 - T3174 COSM4680892 c.905G>A p.R302Q Substitution - Missense 11:62608986-62608986 - BD124T COSM5492806 c.688C>A p.P230T Substitution - Missense 11:62609424-62609424 - CHC1611T COSM4789257 c.511T>G p.S171A Substitution - Missense 11:62610934-62610934 - TCGA-70-6722-01 COSM4862520 c.667C>T p.R223C Substitution - Missense 11:62609445-62609445 - TCGA-BT-A3PJ-01 COSM3451025 c.1074C>T p.F358F Substitution - coding silent 11:62608578-62608578 - YUJUBE COSM3451028 c.657C>T p.F219F Substitution - coding silent 11:62609455-62609455 - C135 COSM4617167 c.1963G>A p.V655I Substitution - Missense 11:62605132-62605132 - TCGA-BS-A0TJ-01 COSM4868183 c.1416C>T p.D472D Substitution - coding silent 11:62607046-62607046 - SNU-175 COSM4198876 c.2153G>A p.R718H Substitution - Missense 11:62603960-62603960 - PTC-7C COSM4146013 c.210A>G p.P70P Substitution - coding silent 11:62611329-62611329 - PTC-28C COSM4146011 c.351C>T p.S117S Substitution - coding silent 11:62611188-62611188 - TCGA-RP-A694-06 COSM4894386 c.325C>T p.P109S Substitution - Missense 11:62611214-62611214 - 587342 COSM1205260 c.728C>A p.P243Q Substitution - Missense 11:62609384-62609384 - SCC-15 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - 2497781 COSM5750828 c.586C>G p.L196V Substitution - Missense 11:62609677-62609677 - PCSI_0083_Pa_P_526 COSM2039059 c.553G>A p.G185R Substitution - Missense 11:62610892-62610892 - TCGA-EE-A2MS-06 COSM3451024 c.1074C>T p.F358F Substitution - coding silent 11:62608578-62608578 - HCC031T COSM5807801 c.2642C>A p.T881K Substitution - Missense 11:62602524-62602524 - T2940 COSM4680895 c.210delA p.G71fs*11 Deletion - Frameshift 11:62611329-62611329 - TCGA-FW-A3R5-06 COSM3869758 c.834C>T p.A278A Substitution - coding silent 11:62609057-62609057 - TCGA-A6-5665-01 COSM5089764 c.1783-5T>C p.? Unknown 11:62605778-62605778 - CSCC-55-T COSM4460259 c.1159C>T p.L387L Substitution - coding silent 11:62608248-62608248 - TCGA-R2-A69V-01 COSM4851203 c.972G>C p.Q324H Substitution - Missense 11:62608763-62608763 - SM-4AX82 COSM5036791 c.1129T>C p.C377R Substitution - Missense 11:62608278-62608278 - Esp66 COSM1742583 c.2245G>C p.E749Q Substitution - Missense 11:62603741-62603741 - BD235T COSM5501642 c.340G>C p.E114Q Substitution - Missense 11:62611199-62611199 - TCGA-24-1849-01 COSM429450 c.212_213insG p.L72fs*46 Insertion - Frameshift 11:62611326-62611327 - TCGA-DK-A3IT-01 COSM1298313 c.499C>T p.R167W Substitution - Missense 11:62610946-62610946 - TCGA-EE-A2MR-06 COSM3451029 c.657C>T p.F219F Substitution - coding silent 11:62609455-62609455 - TCGA-FW-A3TV-06 COSM3451021 c.1282C>T p.H428Y Substitution - Missense 11:62607746-62607746 - ESCC_BICR_019T COSM5431513 c.890G>A p.G297D Substitution - Missense 11:62609001-62609001 - TCGA-BS-A0TA-01 COSM929733 c.126C>T p.R42R Substitution - coding silent 11:62611493-62611493 - TCGA-A2-A04V-01 COSM429449 c.1995G>A p.L665L Substitution - coding silent 11:62604189-62604189 - PS-352-2D COSM4423968 c.2337G>C p.V779V Substitution - coding silent 11:62603168-62603168 - PS-352-1D COSM4423967 c.2337G>C p.V779V Substitution - coding silent 11:62603168-62603168 - CSCC-27-T COSM4498939 c.530C>T p.S177F Substitution - Missense 11:62610915-62610915 - TCGA-D9-A6EC-06 COSM4404329 c.1293C>T p.F431F Substitution - coding silent 11:62607735-62607735 - 418 COSM4431805 c.2392G>A p.V798I Substitution - Missense 11:62602664-62602664 - 5853_CLM COSM5753754 c.43G>T p.A15S Substitution - Missense 11:62611576-62611576 - TCGA-DD-A4NI-01 COSM4926352 c.897A>G p.R299R Substitution - coding silent 11:62608994-62608994 - PT14_1 COSM5897003 c.644C>T p.S215L Substitution - Missense 11:62609468-62609468 - 345973 COSM3726587 c.2100T>C p.H700H Substitution - coding silent 11:62604013-62604013 - T3021 COSM4680889 c.1498G>A p.A500T Substitution - Missense 11:62606964-62606964 - WSU-HN8 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - YUMOBER COSM5373091 c.1157T>G p.M386R Substitution - Missense 11:62608250-62608250 - TCGA-AA-3672-01 COSM266456 c.1949G>T p.G650V Substitution - Missense 11:62605146-62605146 - UD-SCC-2 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - TCGA-D5-6928-01 COSM5165533 c.835T>C p.C279R Substitution - Missense 11:62609056-62609056 - TCGA-FW-A3R5-06 COSM3869757 c.834C>T p.A278A Substitution - coding silent 11:62609057-62609057 - CAL33 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - PD9755a COSM5782692 c.699C>T p.I233I Substitution - coding silent 11:62609413-62609413 - T3064 COSM4680897 c.209_210insC p.G71fs*47 Insertion - Frameshift 11:62611329-62611330 - TCGA-EP-A2KB-01 COSM4921327 c.2326T>C p.Y776H Substitution - Missense 11:62603179-62603179 - TCGA-66-2756-01 COSM4862504 c.1774G>A p.V592I Substitution - Missense 11:62605863-62605863 - ACINAR01 COSM1735069 c.1906G>A p.D636N Substitution - Missense 11:62605650-62605650 - UM-SCC-17B COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - TCGA-EE-A2MS-06 COSM3451025 c.1074C>T p.F358F Substitution - coding silent 11:62608578-62608578 - TCGA-AP-A059-01 COSM929732 c.171C>T p.G57G Substitution - coding silent 11:62611448-62611448 - TCGA-EE-A3J4-06 COSM3869754 c.1770C>T p.S590S Substitution - coding silent 11:62605867-62605867 - SNU-C4 COSM4651999 c.2056G>A p.V686I Substitution - Missense 11:62604128-62604128 - TCGA-EU-5904-01 COSM467143 c.1616T>G p.V539G Substitution - Missense 11:62606103-62606103 - T3262 COSM2039058 c.575delG p.G192fs*25 Deletion - Frameshift 11:62609688-62609688 - sysucc-880T COSM5462055 c.1334C>T p.T445I Substitution - Missense 11:62607694-62607694 - TCGA-36-2534-01 COSM1322299 c.1371G>C p.K457N Substitution - Missense 11:62607091-62607091 - P-Thy018 COSM5095364 c.2498G>T p.R833L Substitution - Missense 11:62602668-62602668 - TCGA-EE-A2MR-06 COSM3451028 c.657C>T p.F219F Substitution - coding silent 11:62609455-62609455 - RMS2030 COSM5880540 c.442C>T p.R148C Substitution - Missense 11:62611097-62611097 - PT14_1 COSM5897004 c.644C>T p.S215L Substitution - Missense 11:62609468-62609468 - PTC-7C COSM4146008 c.2623G>C p.A875P Substitution - Missense 11:62602433-62602433 - TCGA-F5-6814-01 COSM3416066 c.1731G>T p.K577N Substitution - Missense 11:62605906-62605906 - TCGA-CK-5916-01 COSM3686032 c.212_213insG p.L72fs*46 Insertion - Frameshift 11:62611326-62611327 - LS180 COSM4614388 c.602delG p.G201fs*16 Deletion - Frameshift 11:62609661-62609661 - CSCC-38-T COSM4470117 c.1641C>T p.A547A Substitution - coding silent 11:62606078-62606078 - HCC61T COSM3666474 c.480A>G p.S160S Substitution - coding silent 11:62610965-62610965 - CSCC-44-T COSM4562016 c.908G>A p.G303E Substitution - Missense 11:62608983-62608983 - CSCC-27-T COSM4498940 c.530C>T p.S177F Substitution - Missense 11:62610915-62610915 - TCGA-A8-A0A6-01 COSM3809838 c.861A>G p.G287G Substitution - coding silent 11:62609030-62609030 - TCGA-EB-A5UN-06 COSM3451030 c.591C>T p.S197S Substitution - coding silent 11:62609672-62609672 - Pat_04_A COSM5839056 c.604C>T p.P202S Substitution - Missense 11:62609659-62609659 - CSCC-18-T COSM4513249 c.931C>T p.L311F Substitution - Missense 11:62608804-62608804 - KYSE-150 COSM2039014 c.2386G>A p.D796N Substitution - Missense 11:62602860-62602860 - TCGA-FW-A3R5-06 COSM3869751 c.1926C>T p.L642L Substitution - coding silent 11:62605169-62605169 - CSCC-44-T COSM4562015 c.908G>A p.G303E Substitution - Missense 11:62608983-62608983 - TCGA-AM-5821-01 COSM5134760 c.637G>T p.G213C Substitution - Missense 11:62609475-62609475 - BD6T COSM5499101 c.1122C>A p.A374A Substitution - coding silent 11:62608285-62608285 - TCGA-GN-A26C-01 COSM3451023 c.1137G>T p.V379V Substitution - coding silent 11:62608270-62608270 - TCGA-HU-A4G9-01 COSM4034807 c.614G>T p.R205L Substitution - Missense 11:62609649-62609649 - TCGA-DD-A73D-01 COSM4935349 c.1527G>A p.Q509Q Substitution - coding silent 11:62606192-62606192 - TCGA-HU-A4GU-01 COSM4034810 c.404G>A p.G135D Substitution - Missense 11:62611135-62611135 - T84 COSM2039054 c.744C>G p.L248L Substitution - coding silent 11:62609368-62609368 - BN24T COSM1604909 c.1008G>A p.Q336Q Substitution - coding silent 11:62608644-62608644 - TCGA-AC-A23H-01 COSM3809840 c.562G>A p.E188K Substitution - Missense 11:62610883-62610883 - T3064 COSM4680896 c.209_210insC p.G71fs*47 Insertion - Frameshift 11:62611329-62611330 - pfg008T COSM1355404 c.209delC p.P70fs*12 Deletion - Frameshift 11:62611330-62611330 - PTC-28C COSM4146010 c.351C>T p.S117S Substitution - coding silent 11:62611188-62611188 - TCGA-AP-A051-01 COSM929730 c.700C>T p.R234C Substitution - Missense 11:62609412-62609412 - 2521262 COSM5892126 c.1983-8C>T p.? Unknown 11:62604209-62604209 - TCGA-AN-A046-01 COSM3809836 c.2289G>T p.K763N Substitution - Missense 11:62603216-62603216 - ATL085 COSM5704109 c.896G>C p.R299T Substitution - Missense 11:62608995-62608995 - SCC-25 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - TCGA-BR-8078-01 COSM4034801 c.1013T>C p.V338A Substitution - Missense 11:62608639-62608639 - sysucc-880T COSM5462057 c.36T>C p.A12A Substitution - coding silent 11:62611583-62611583 - TCGA-32-2491-01 COSM3397989 c.343G>T p.E115* Substitution - Nonsense 11:62611196-62611196 - TCGA-AD-6889-01 COSM1355399 c.2017G>A p.V673M Substitution - Missense 11:62604167-62604167 - 224 COSM4425595 c.1717G>A p.V573M Substitution - Missense 11:62605920-62605920 - TCGA-HU-A4G9-01 COSM4034808 c.614G>T p.R205L Substitution - Missense 11:62609649-62609649 - TCGA-BR-4362-01 COSM4034797 c.1209T>C p.S403S Substitution - coding silent 11:62607819-62607819 - PTC-28C COSM429448 c.2488-5C>T p.? Unknown 11:62602683-62602683 - sysucc-1024T COSM5763151 c.1422C>T p.L474L Substitution - coding silent 11:62607040-62607040 - H1155 COSM1195166 c.668G>A p.R223H Substitution - Missense 11:62609444-62609444 - TCGA-AZ-4614-01 COSM5139357 c.817G>T p.V273L Substitution - Missense 11:62609074-62609074 - HCC61 COSM3666474 c.480A>G p.S160S Substitution - coding silent 11:62610965-62610965 - sysucc-880T COSM5462056 c.36T>C p.A12A Substitution - coding silent 11:62611583-62611583 - Detroit_562 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - S00838 COSM5661424 c.79G>C p.E27Q Substitution - Missense 11:62611540-62611540 - TCGA-AP-A059-01 COSM4198937 c.171C>T p.G57G Substitution - coding silent 11:62611448-62611448 - TCGA-A5-A0GW-01 COSM929724 c.2270G>A p.G757E Substitution - Missense 11:62603235-62603235 - SNU-175 COSM4198908 c.805C>T p.R269C Substitution - Missense 11:62609086-62609086 - TCGA-60-2698-01 COSM4860769 c.504G>A p.Q168Q Substitution - coding silent 11:62610941-62610941 - S01576 COSM4387266 c.1760A>T p.Q587L Substitution - Missense 11:62605877-62605877 - Pat_05_A COSM5839052 c.2561delG p.R854fs*7 Deletion - Frameshift 11:62602495-62602495 - TCGA-GN-A26C-01 COSM544064 c.1137G>T p.V379V Substitution - coding silent 11:62608270-62608270 - S01576 COSM4387267 c.1760A>T p.Q587L Substitution - Missense 11:62605877-62605877 - TCGA-AA-3511-01 COSM5100314 c.759-3C>T p.? Unknown 11:62609135-62609135 - TCGA-CD-5801-01 COSM4034806 c.700C>T p.R234C Substitution - Missense 11:62609412-62609412 - T2940 COSM4680894 c.210delA p.G71fs*11 Deletion - Frameshift 11:62611329-62611329 - SC_9093 COSM5555191 c.889G>A p.G297S Substitution - Missense 11:62609002-62609002 - TCGA-RP-A693-06 COSM4896003 c.1628C>T p.P543L Substitution - Missense 11:62606091-62606091 - 587222 COSM1205258 c.334G>A p.A112T Substitution - Missense 11:62611205-62611205 - 2497781 COSM5750829 c.586C>G p.L196V Substitution - Missense 11:62609677-62609677 - TCGA-AP-A051-01 COSM4034806 c.700C>T p.R234C Substitution - Missense 11:62609412-62609412 - CHC1611T COSM4789258 c.511T>G p.S171A Substitution - Missense 11:62610934-62610934 - TCGA-JX-A3Q0-01 COSM4824426 c.1603G>C p.D535H Substitution - Missense 11:62606116-62606116 - TCGA-FW-A3TV-06 COSM3451022 c.1282C>T p.H428Y Substitution - Missense 11:62607746-62607746 - sysucc-880T COSM5462054 c.1334C>T p.T445I Substitution - Missense 11:62607694-62607694 - TCGA-AP-A059-01 COSM929723 c.2317T>G p.W773G Substitution - Missense 11:62603188-62603188 - TCGA-EB-A42Z-01 COSM3451018 c.1606C>T p.R536C Substitution - Missense 11:62606113-62606113 - TCGA-EE-A2MR-06 COSM3451020 c.1554C>T p.F518F Substitution - coding silent 11:62606165-62606165 - TCGA-CH-5791-01 COSM4879234 c.346C>T p.P116S Substitution - Missense 11:62611193-62611193 - TCGA-DK-A1AC-01 COSM1298311 c.1926C>G p.L642L Substitution - coding silent 11:62605169-62605169 - 8051707 COSM4406565 c.1817A>C p.H606P Substitution - Missense 11:62605739-62605739 - TCGA-A6-6781-01 COSM5093315 c.149delC p.P50fs*32 Deletion - Frameshift 11:62611470-62611470 - Gp2D COSM929732 c.171C>T p.G57G Substitution - coding silent 11:62611448-62611448 - CN-AML-CR-27-Dx COSM5424504 c.54T>C p.S18S Substitution - coding silent 11:62611565-62611565 - Pat_26_A COSM2039035 c.1459C>T p.R487W Substitution - Missense 11:62607003-62607003 - BN24 COSM3666473 c.1008G>A p.Q336Q Substitution - coding silent 11:62608644-62608644 - GC_370T-GC_370N COSM4773140 c.84G>T p.Q28H Substitution - Missense 11:62611535-62611535 - CN-AML-CR-27-Dx COSM5424505 c.54T>C p.S18S Substitution - coding silent 11:62611565-62611565 - TCGA-CD-5801-01 COSM929730 c.700C>T p.R234C Substitution - Missense 11:62609412-62609412 - TCGA-AA-3492-01 COSM5096812 c.2658_2659insC p.S887fs*>11 Insertion - Frameshift 11:62602507-62602508 - T3174 COSM4680893 c.905G>A p.R302Q Substitution - Missense 11:62608986-62608986 - HCC61 COSM1604910 c.480A>G p.S160S Substitution - coding silent 11:62610965-62610965 - CSCC-45-T COSM4565203 c.1854_1855CC>TT p.R619W Substitution - Missense 11:62605701-62605702 - TCGA-G4-6588-01 COSM4782671 c.913A>G p.T305A Substitution - Missense 11:62608978-62608978 - TCGA-CG-4437-01 COSM4034794 c.1407G>A p.P469P Substitution - coding silent 11:62607055-62607055 - I2L-P25-Tumor-Organoid COSM5360918 c.296C>T p.P99L Substitution - Missense 11:62611243-62611243 - 0063_CRUK_PC_0063_T1_DNA COSM5420783 c.2745C>T p.H915H Substitution - coding silent 11:62602311-62602311 - BICR_22 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - TCGA-BR-8078-01 COSM4034800 c.1013T>C p.V338A Substitution - Missense 11:62608639-62608639 - PD11372a COSM5793154 c.1080G>T p.R360R Substitution - coding silent 11:62608572-62608572 - T3724 COSM4680891 c.926G>A p.R309Q Substitution - Missense 11:62608965-62608965 - TCGA-EB-A42Z-01 COSM3451017 c.1606C>T p.R536C Substitution - Missense 11:62606113-62606113 - PCSI_0083_Pa_P_526 COSM3788019 c.553G>A p.G185R Substitution - Missense 11:62610892-62610892 - SNU-C4 COSM4651998 c.2056G>A p.V686I Substitution - Missense 11:62604128-62604128 - TCGA-DD-A73D-01 COSM4935348 c.1527G>A p.Q509Q Substitution - coding silent 11:62606192-62606192 - ATL085 COSM5704108 c.896G>C p.R299T Substitution - Missense 11:62608995-62608995 - PD11372a COSM5793155 c.1080G>T p.R360R Substitution - coding silent 11:62608572-62608572 - 2492729 COSM5729764 c.1946G>C p.S649T Substitution - Missense 11:62605149-62605149 - 2521262 COSM5892127 c.1983-8C>T p.? Unknown 11:62604209-62604209 - TCGA-D1-A16B-01 COSM929731 c.548G>A p.R183Q Substitution - Missense 11:62610897-62610897 - TCGA-AP-A059-01 COSM929726 c.2112C>T p.I704I Substitution - coding silent 11:62604001-62604001 - UPCI:SCC090 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - TCGA-BS-A0TJ-01 COSM929728 c.1416C>T p.D472D Substitution - coding silent 11:62607046-62607046 - C086 COSM5530450 c.1471G>A p.D491N Substitution - Missense 11:62606991-62606991 - BCB157T COSM4949935 c.2405G>A p.R802H Substitution - Missense 11:62602841-62602841 - TCGA-FD-A3SO-01 COSM2039069 c.181C>T p.P61S Substitution - Missense 11:62611438-62611438 - YUJUBE COSM3451029 c.657C>T p.F219F Substitution - coding silent 11:62609455-62609455 - TCGA-F5-6814-01 COSM1205261 c.1731G>T p.K577N Substitution - Missense 11:62605906-62605906 - WSU-HN6 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - 4989_PT COSM5753752 c.158T>C p.L53P Substitution - Missense 11:62611461-62611461 - TCGA-AD-6889-01 COSM1355404 c.209delC p.P70fs*12 Deletion - Frameshift 11:62611330-62611330 - TCGA-CK-5916-01 COSM4680896 c.209_210insC p.G71fs*47 Insertion - Frameshift 11:62611329-62611330 - LS180 COSM4614387 c.602delG p.G201fs*16 Deletion - Frameshift 11:62609661-62609661 - BD62T COSM5498667 c.1540G>A p.E514K Substitution - Missense 11:62606179-62606179 - TCGA-R2-A69V-01 COSM4851204 c.972G>C p.Q324H Substitution - Missense 11:62608763-62608763 - 418 COSM4431804 c.2502G>A p.M834I Substitution - Missense 11:62602664-62602664 - LAU165 COSM232246 c.574G>A p.G192R Substitution - Missense 11:62609689-62609689 - WSU-HN12 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - 587370 COSM1205259 c.569G>A p.R190H Substitution - Missense 11:62609694-62609694 - TCGA-CD-A4MG-01 COSM4034798 c.1050G>A p.L350L Substitution - coding silent 11:62608602-62608602 - CN-AML-CR-16-Dx COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - ORL-48 COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - TCGA-DK-A1AC-01 COSM4811916 c.1926C>G p.L642L Substitution - coding silent 11:62605169-62605169 - TCGA-66-2793-01 COSM689191 c.2041G>C p.E681Q Substitution - Missense 11:62604143-62604143 - S01023 COSM5666384 c.1720G>T p.G574* Substitution - Nonsense 11:62605917-62605917 - TCGA-BH-A1FL-01 COSM1241126 c.531C>T p.S177S Substitution - coding silent 11:62610914-62610914 - TCGA-A8-A0A6-01 COSM3809837 c.861A>G p.G287G Substitution - coding silent 11:62609030-62609030 - OCC05PT COSM88720 c.1906_1909delGACC p.D636fs*19 Deletion - Frameshift 11:62605647-62605650 - P-Thy018 COSM5095365 c.2388G>T p.P796P Substitution - coding silent 11:62602668-62602668 - RMS2030 COSM5880541 c.442C>T p.R148C Substitution - Missense 11:62611097-62611097 - TCGA-D3-A1Q6-06 COSM3451026 c.688C>T p.P230S Substitution - Missense 11:62609424-62609424 - Gp2D COSM4198937 c.171C>T p.G57G Substitution - coding silent 11:62611448-62611448 - TCGA-LP-A4AW-01 COSM4829766 c.2705C>T p.S902L Substitution - Missense 11:62602351-62602351 - TCGA-A3-3316-01 COSM467144 c.1303A>G p.S435G Substitution - Missense 11:62607725-62607725 - S01023 COSM5666383 c.1720G>T p.G574* Substitution - Nonsense 11:62605917-62605917 - TCGA-66-2793-01 COSM4859781 c.2041G>C p.E681Q Substitution - Missense 11:62604143-62604143 - C086 COSM5530451 c.1471G>A p.D491N Substitution - Missense 11:62606991-62606991 - HN_00122 COSM122832 c.433C>A p.P145T Substitution - Missense 11:62611106-62611106 - TCGA-D5-6530-01 COSM5162164 c.170G>A p.G57D Substitution - Missense 11:62611449-62611449 - 587376 COSM1205261 c.1731G>T p.K577N Substitution - Missense 11:62605906-62605906 - CSCC-31-T COSM4531499 c.1795G>T p.E599* Substitution - Nonsense 11:62605761-62605761 - SC_9093 COSM5555190 c.889G>A p.G297S Substitution - Missense 11:62609002-62609002 - TCGA-A2-A0CU-01 COSM4680896 c.209_210insC p.G71fs*47 Insertion - Frameshift 11:62611329-62611330 - E15 COSM1666412 c.2258-4C>T p.? Unknown 11:62603251-62603251 - TCGA-D3-A1Q6-06 COSM3451027 c.688C>T p.P230S Substitution - Missense 11:62609424-62609424 - T36 COSM4680896 c.209_210insC p.G71fs*47 Insertion - Frameshift 11:62611329-62611330 - ESCC_BICR_070T COSM5444829 c.467C>G p.S156C Substitution - Missense 11:62610978-62610978 - RKO COSM4647394 c.2320G>A p.A774T Substitution - Missense 11:62603185-62603185 - TCGA-AP-A059-01 COSM4866845 c.2317T>G p.W773G Substitution - Missense 11:62603188-62603188 - LUAD-S01315 COSM344039 c.1184G>T p.G395V Substitution - Missense 11:62608223-62608223 - CSCC-38-T COSM4470118 c.1641C>T p.A547A Substitution - coding silent 11:62606078-62606078 - TCGA-D1-A16B-01 COSM4865051 c.548G>A p.R183Q Substitution - Missense 11:62610897-62610897 - 224 COSM4425594 c.1717G>A p.V573M Substitution - Missense 11:62605920-62605920 - TCGA-AP-A059-01 COSM4866559 c.2112C>T p.I704I Substitution - coding silent 11:62604001-62604001 - TCGA-AN-A046-01 COSM3809835 c.2289G>T p.K763N Substitution - Missense 11:62603216-62603216 - MO_1013 COSM5571125 c.841G>T p.V281L Substitution - Missense 11:62609050-62609050 - 587220 COSM1205256 c.832G>A p.A278T Substitution - Missense 11:62609059-62609059 - TCGA-DD-A4NI-01 COSM4926353 c.897A>G p.R299R Substitution - coding silent 11:62608994-62608994 - BD62T COSM5498668 c.1540G>A p.E514K Substitution - Missense 11:62606179-62606179 - EGC3 COSM4747360 c.209delC p.P70fs*12 Deletion - Frameshift 11:62611330-62611330 - TCGA-FP-8099-01 COSM4034803 c.806G>A p.R269H Substitution - Missense 11:62609085-62609085 - 1758083 COSM308566 c.356C>A p.T119N Substitution - Missense 11:62611183-62611183 - ESO-2143 COSM1251166 c.1888G>A p.A630T Substitution - Missense 11:62605668-62605668 - 345973 COSM2039022 c.2100T>C p.H700H Substitution - coding silent 11:62604013-62604013 - TCGA-EE-A2MS-06 COSM3451015 c.1836C>A p.F612L Substitution - Missense 11:62605720-62605720 - TCGA-EU-5904-01 COSM4858225 c.1616T>G p.V539G Substitution - Missense 11:62606103-62606103 - TCGA-AA-3811-01 COSM5108599 c.1469C>A p.S490* Substitution - Nonsense 11:62606993-62606993 - TCGA-EE-A29V-06 COSM3451033 c.473C>T p.S158F Substitution - Missense 11:62610972-62610972 - TCGA-CG-4437-01 COSM4034795 c.1407G>A p.P469P Substitution - coding silent 11:62607055-62607055 - ATL015 COSM5704110 c.31C>T p.P11S Substitution - Missense 11:62611588-62611588 - HCC051T COSM5820683 c.2139T>A p.G713G Substitution - coding silent 11:62603974-62603974 - TCGA-BT-A2LA-01 COSM1298312 c.564G>C p.E188D Substitution - Missense 11:62610881-62610881 - HCC61T COSM1604910 c.480A>G p.S160S Substitution - coding silent 11:62610965-62610965 - CSCC-55-T COSM4460258 c.1159C>T p.L387L Substitution - coding silent 11:62608248-62608248 - T3262 COSM4680899 c.139C>T p.Q47* Substitution - Nonsense 11:62611480-62611480 - PTC-28C COSM4146007 c.2644G>C p.A882P Substitution - Missense 11:62602412-62602412 - TCGA-BS-A0UV-01 COSM929725 c.2192A>G p.H731R Substitution - Missense 11:62603794-62603794 - 4989_PT COSM5753751 c.158T>C p.L53P Substitution - Missense 11:62611461-62611461 - ATL015 COSM5704111 c.31C>T p.P11S Substitution - Missense 11:62611588-62611588 - TCGA-RP-A693-06 COSM4896004 c.1628C>T p.P543L Substitution - Missense 11:62606091-62606091 - Pat_26_A COSM4198894 c.1459C>T p.R487W Substitution - Missense 11:62607003-62607003 - I2L-P25-Tumor-Organoid COSM5360919 c.296C>T p.P99L Substitution - Missense 11:62611243-62611243 - TCGA-FP-8099-01 COSM4034802 c.806G>A p.R269H Substitution - Missense 11:62609085-62609085 - TCGA-EB-A5UN-06 COSM3451031 c.591C>T p.S197S Substitution - coding silent 11:62609672-62609672 - TCGA-BH-A1FL-01 COSM4814538 c.531C>T p.S177S Substitution - coding silent 11:62610914-62610914 - BD6T COSM5499102 c.1122C>A p.A374A Substitution - coding silent 11:62608285-62608285 - TCGA-RP-A694-06 COSM4894385 c.325C>T p.P109S Substitution - Missense 11:62611214-62611214 - T368 COSM4680894 c.210delA p.G71fs*11 Deletion - Frameshift 11:62611329-62611329 - T3021 COSM4680888 c.1498G>A p.A500T Substitution - Missense 11:62606964-62606964 - TCGA-FW-A3R5-06 COSM3869752 c.1926C>T p.L642L Substitution - coding silent 11:62605169-62605169 - Gp5D COSM4198937 c.171C>T p.G57G Substitution - coding silent 11:62611448-62611448 - TCGA-EE-A29V-06 COSM2039065 c.288C>T p.S96S Substitution - coding silent 11:62611251-62611251 - TCGA-A2-A0CU-01 COSM4680897 c.209_210insC p.G71fs*47 Insertion - Frameshift 11:62611329-62611330 - BCB157T COSM4949935 c.2405G>A p.R802H Substitution - Missense 11:62602841-62602841 - Pat_05_A COSM5839051 c.2671delG p.A891fs*>6 Deletion - Frameshift 11:62602495-62602495 - SM-4AX82 COSM5036790 c.1129T>C p.C377R Substitution - Missense 11:62608278-62608278 - BD235T COSM5501643 c.340G>C p.E114Q Substitution - Missense 11:62611199-62611199 - TCGA-CK-5916-01 COSM429450 c.212_213insG p.L72fs*46 Insertion - Frameshift 11:62611326-62611327 - TCGA-AD-6889-01 COSM4747360 c.209delC p.P70fs*12 Deletion - Frameshift 11:62611330-62611330 - TCGA-EE-A2MR-06 COSM3451019 c.1554C>T p.F518F Substitution - coding silent 11:62606165-62606165 - T3262 COSM4680898 c.139C>T p.Q47* Substitution - Nonsense 11:62611480-62611480 - TCGA-EE-A2MS-06 COSM3451016 c.1836C>A p.F612L Substitution - Missense 11:62605720-62605720 - TCGA-ES-A2HT-01 COSM4938729 c.1186A>G p.M396V Substitution - Missense 11:62608221-62608221 - ESCC_BICR_070T COSM5444828 c.467C>G p.S156C Substitution - Missense 11:62610978-62610978 - Gp5D COSM929732 c.171C>T p.G57G Substitution - coding silent 11:62611448-62611448 - CSCC-18-T COSM4513250 c.931C>T p.L311F Substitution - Missense 11:62608804-62608804 - MO_1013 COSM5571124 c.841G>T p.V281L Substitution - Missense 11:62609050-62609050 - 313 COSM1741964 c.2299G>C p.E767Q Substitution - Missense 11:62603206-62603206 - TCGA-D1-A17Q-01 COSM929729 c.1163C>T p.S388L Substitution - Missense 11:62608244-62608244 - TCGA-C5-A1MK-01 COSM2039015 c.2377G>A p.D793N Substitution - Missense 11:62602869-62602869 - 8051707 COSM4406564 c.1817A>C p.H606P Substitution - Missense 11:62605739-62605739 - Pat_04_A COSM5839055 c.604C>T p.P202S Substitution - Missense 11:62609659-62609659 - TCGA-CD-A4MG-01 COSM4034799 c.1050G>A p.L350L Substitution - coding silent 11:62608602-62608602 - TCGA-FW-A3R5-06 COSM3451019 c.1554C>T p.F518F Substitution - coding silent 11:62606165-62606165 - T36 COSM4680897 c.209_210insC p.G71fs*47 Insertion - Frameshift 11:62611329-62611330 - 5853_CLM COSM5753753 c.43G>T p.A15S Substitution - Missense 11:62611576-62611576 - LUAD-5V8LT COSM401224 c.437C>A p.P146Q Substitution - Missense 11:62611102-62611102 - YUMOBER COSM5373092 c.1157T>G p.M386R Substitution - Missense 11:62608250-62608250 - EGC3 COSM1355404 c.209delC p.P70fs*12 Deletion - Frameshift 11:62611330-62611330 - TCGA-EE-A29V-06 COSM3451034 c.288C>T p.S96S Substitution - coding silent 11:62611251-62611251 - CSCC-45-T COSM4565204 c.1854_1855CC>TT p.R619W Substitution - Missense 11:62605701-62605702 - RKO COSM4647393 c.2320G>A p.A774T Substitution - Missense 11:62603185-62603185 - GC_370T-GC_370N COSM4773139 c.84G>T p.Q28H Substitution - Missense 11:62611535-62611535 - TCGA-A6-6781-01 COSM1355405 c.149delC p.P50fs*32 Deletion - Frameshift 11:62611470-62611470 - TCGA-EE-A2MJ-06 COSM3869756 c.1098C>T p.A366A Substitution - coding silent 11:62608554-62608554 - C135 COSM4617166 c.1963G>A p.V655I Substitution - Missense 11:62605132-62605132 - TCGA-FD-A3SO-01 COSM3791703 c.181C>T p.P61S Substitution - Missense 11:62611438-62611438 - TCGA-BS-A0UV-01 COSM4864480 c.2192A>G p.H731R Substitution - Missense 11:62603794-62603794 - TARGET-30-PAIFXV COSM1284728 c.914C>T p.T305I Substitution - Missense 11:62608977-62608977 - T3262 COSM4334217 c.575delG p.G192fs*25 Deletion - Frameshift 11:62609688-62609688 - TCGA-DK-A3IT-01 COSM4811339 c.499C>T p.R167W Substitution - Missense 11:62610946-62610946 - TCGA-BR-7851-01 COSM4034805 c.785G>A p.R262H Substitution - Missense 11:62609106-62609106 - 9149_T COSM5038668 c.1440delG p.N481fs*49 Deletion - Frameshift 11:62607022-62607022 - TCGA-BT-A3PJ-01 COSM3451024 c.1074C>T p.F358F Substitution - coding silent 11:62608578-62608578 - sysucc-1024T COSM5763152 c.1422C>T p.L474L Substitution - coding silent 11:62607040-62607040 - BD124T COSM5492807 c.688C>A p.P230T Substitution - Missense 11:62609424-62609424 - TCGA-EP-A2KB-01 COSM4921328 c.2326T>C p.Y776H Substitution - Missense 11:62603179-62603179 - TCGA-70-6722-01 COSM689187 c.667C>T p.R223C Substitution - Missense 11:62609445-62609445 - TCGA-A5-A0GW-01 COSM4872150 c.2270G>A p.G757E Substitution - Missense 11:62603235-62603235 - PD9755a COSM5782699 c.692C>T p.S231F Substitution - Missense 11:62609420-62609420 - T368 COSM4680895 c.210delA p.G71fs*11 Deletion - Frameshift 11:62611329-62611329 - TCGA-D9-A6EC-06 COSM4404328 c.1293C>T p.F431F Substitution - coding silent 11:62607735-62607735 - 9149_T COSM5038667 c.1440delG p.N481fs*49 Deletion - Frameshift 11:62607022-62607022 - LUAD-NYU259 COSM371700 c.666G>T p.G222G Substitution - coding silent 11:62609446-62609446 - PTC-28C COSM4146006 c.2647C>T p.Q883* Substitution - Nonsense 11:62602409-62602409 - 587222 COSM1205257 c.2686G>C p.V896L Substitution - Missense 11:62602480-62602480 - pfg008T COSM4747360 c.209delC p.P70fs*12 Deletion - Frameshift 11:62611330-62611330 - TCGA-A2-A04V-01 COSM4815297 c.1995G>A p.L665L Substitution - coding silent 11:62604189-62604189 - TCGA-EE-A2MJ-06 COSM3869755 c.1098C>T p.A366A Substitution - coding silent 11:62608554-62608554 - T3724 COSM4680890 c.926G>A p.R309Q Substitution - Missense 11:62608965-62608965 - BN24 COSM1604909 c.1008G>A p.Q336Q Substitution - coding silent 11:62608644-62608644 - TCGA-D1-A17Q-01 COSM4865253 c.1163C>T p.S388L Substitution - Missense 11:62608244-62608244 - PD9755a COSM5782691 c.699C>T p.I233I Substitution - coding silent 11:62609413-62609413 - TCGA-FW-A3R5-06 COSM3451020 c.1554C>T p.F518F Substitution - coding silent 11:62606165-62606165 - TCGA-CH-5791-01 COSM1127707 c.346C>T p.P116S Substitution - Missense 11:62611193-62611193 - Pat_30_A COSM5839054 c.1069delG p.A357fs*40 Deletion - Frameshift 11:62608583-62608583 - T84 COSM4198913 c.744C>G p.L248L Substitution - coding silent 11:62609368-62609368 - SNU-175 COSM2039020 c.2153G>A p.R718H Substitution - Missense 11:62603960-62603960 - BN24T COSM3666473 c.1008G>A p.Q336Q Substitution - coding silent 11:62608644-62608644 - CSCC-31-T COSM4531500 c.1795G>T p.E599* Substitution - Nonsense 11:62605761-62605761 - PTC-28C COSM4146009 c.2378-5C>T p.? Unknown 11:62602683-62602683 - TCGA-HU-A4GU-01 COSM4034809 c.404G>A p.G135D Substitution - Missense 11:62611135-62611135 - PTC-7C COSM4146012 c.210A>G p.P70P Substitution - coding silent 11:62611329-62611329 - HCC031T COSM5807802 c.2532C>A p.H844Q Substitution - Missense 11:62602524-62602524 - TCGA-JX-A3Q0-01 COSM4824425 c.1603G>C p.D535H Substitution - Missense 11:62606116-62606116 - TCGA-66-2756-01 COSM689189 c.1774G>A p.V592I Substitution - Missense 11:62605863-62605863 - PT20_2 COSM2039015 c.2377G>A p.D793N Substitution - Missense 11:62602869-62602869 - SNU-175 COSM2039049 c.805C>T p.R269C Substitution - Missense 11:62609086-62609086 - ESCC_BICR_018T COSM5429042 c.1464C>T p.S488S Substitution - coding silent 11:62606998-62606998 - 420 COSM4432021 c.819G>A p.V273V Substitution - coding silent 11:62609072-62609072 - TCGA-ES-A2HT-01 COSM4938730 c.1186A>G p.M396V Substitution - Missense 11:62608221-62608221 - TCGA-D1-A167-01 COSM929727 c.1607G>A p.R536H Substitution - Missense 11:62606112-62606112 - TCGA-BR-7851-01 COSM4034804 c.785G>A p.R262H Substitution - Missense 11:62609106-62609106 - TCGA-AC-A23H-01 COSM3809839 c.562G>A p.E188K Substitution - Missense 11:62610883-62610883 - ESO-0292 COSM1241126 c.531C>T p.S177S Substitution - coding silent 11:62610914-62610914 - Pat_30_A COSM5839053 c.1069delG p.A357fs*40 Deletion - Frameshift 11:62608583-62608583 - S00838 COSM5661423 c.79G>C p.E27Q Substitution - Missense 11:62611540-62611540 - TCGA-BR-4362-01 COSM4034796 c.1209T>C p.S403S Substitution - coding silent 11:62607819-62607819 - PS-352-1D COSM4423968 c.2337G>C p.V779V Substitution - coding silent 11:62603168-62603168 - TCGA-32-2491-01 COSM3397990 c.343G>T p.E115* Substitution - Nonsense 11:62611196-62611196 - ESCC_BICR_019T COSM5431512 c.890G>A p.G297D Substitution - Missense 11:62609001-62609001 - TCGA-60-2698-01 COSM689186 c.504G>A p.Q168Q Substitution - coding silent 11:62610941-62610941 - LUAD-F00162 COSM366079 c.352_353GG>TT p.G118>? Complex 11:62611186-62611187 - 2492729 COSM5729765 c.1946G>C p.S649T Substitution - Missense 11:62605149-62605149 - 420 COSM4432020 c.819G>A p.V273V Substitution - coding silent 11:62609072-62609072 - TCGA-D1-A167-01 COSM4871613 c.1607G>A p.R536H Substitution - Missense 11:62606112-62606112 - TCGA-EE-A29V-06 COSM3451032 c.473C>T p.S158F Substitution - Missense 11:62610972-62610972 - TCGA-G4-6588-01 COSM1355401 c.913A>G p.T305A Substitution - Missense 11:62608978-62608978 - CHC1611T COSM4789258 c.511T>G p.S171A Substitution - Missense 11:62610934-62610934 - PS-352-2D COSM4423967 c.2337G>C p.V779V Substitution - coding silent 11:62603168-62603168 - HCC051T COSM5820684 c.2139T>A p.G713G Substitution - coding silent 11:62603974-62603974 - CHC1611T COSM4789257 c.511T>G p.S171A Substitution - Missense 11:62610934-62610934 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.379785 11q12.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.V539G c.1616T>G 11 62373575 HNSC A C Missense p.V539G c.1616T>G 11 62373575 RCCC C A Nonsense p.E115* c.343G>T 11 62378668 GBM C A Synonymous p.V379V c.1137G>T 11 62375742 CM C G Missense p.E188D c.564G>C 11 62378353 BLCA C G Missense p.E681Q c.2041G>C 11 62371615 LUSC C T IntronicSNV . c.1982+65G>A 11 62372520 CM C T Missense p.A630T c.1888G>A 11 62373140 ESCA C T Missense p.G757E c.2270G>A 11 62370707 UCEC C T Missense p.R183Q c.548G>A 11 62378369 UCEC C T Missense p.R360Q c.1079G>A 11 62376045 CM C T Missense p.V592I c.1774G>A 11 62373335 LUSC C T Synonymous p.L102L c.306G>A 11 62378705 LUAD C T Synonymous p.P469P c.1407G>A 11 62374527 STAD G A Missense p.P116S c.346C>T 11 62378665 PRAD G A Missense p.P230S c.688C>T 11 62376896 CM G A Missense p.R167W c.499C>T 11 62378418 BLCA G A Missense p.R223C c.667C>T 11 62376917 LUSC G A Missense p.R234C c.700C>T 11 62376884 STAD G A Missense p.S158F c.473C>T 11 62378444 CM G A Missense p.T305I c.914C>T 11 62376449 NB G A Synonymous p.A366A c.1098C>T 11 62376026 CM G A Synonymous p.D472D c.1416C>T 11 62374518 UCEC G A Synonymous p.F358F c.1074C>T 11 62376050 BLCA G A Synonymous p.F358F c.1074C>T 11 62376050 CM G A Synonymous p.F518F c.1554C>T 11 62373637 CM G A Synonymous p.S177S c.531C>T 11 62378386 BRCA G A Synonymous p.S198S c.594C>T 11 62377141 CM G A Synonymous p.S590S c.1770C>T 11 62373339 CM GG AA Missense p.P97S c.288_289delinsTT 11 62378722 CM G T Missense p.F612L c.1836C>A 11 62373192 CM G T Missense p.P145T c.433C>A 11 62378578 HNSC T C Synonymous p.G583G c.1749A>G 11 62373360 LUAD