Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 19 57640347 57640347 + Missense_Mutation SNP A A C TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr19:57640347A>C c.304A>C c.(304-306)Atc>Ctc p.I102L BLCA 19 57640383 57640383 + Missense_Mutation SNP G G T TCGA-DK-AA6Q-01A-11D-A391-08 TCGA-DK-AA6Q-10A-01D-A394-08 g.chr19:57640383G>T c.340G>T c.(340-342)Gat>Tat p.D114Y BLCA 19 57640386 57640386 + Missense_Mutation SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr19:57640386G>A c.343G>A c.(343-345)Gat>Aat p.D115N BLCA 19 57640431 57640431 + Missense_Mutation SNP G G C TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr19:57640431G>C c.388G>C c.(388-390)Gac>Cac p.D130H BLCA 19 57640569 57640569 + Missense_Mutation SNP G G C TCGA-K4-A6MB-01A-11D-A31L-08 TCGA-K4-A6MB-10A-01D-A31J-08 g.chr19:57640569G>C c.526G>C c.(526-528)Gat>Cat p.D176H BLCA 19 57640824 57640824 + Missense_Mutation SNP G G C TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:57640824G>C c.781G>C c.(781-783)Gag>Cag p.E261Q BLCA 19 57640872 57640872 + Missense_Mutation SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:57640872G>A c.829G>A c.(829-831)Gac>Aac p.D277N BLCA 19 57641057 57641057 + Silent SNP G G A TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr19:57641057G>A c.1014G>A c.(1012-1014)ttG>ttA p.L338L BLCA 19 57641088 57641088 + Missense_Mutation SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:57641088G>A c.1045G>A c.(1045-1047)Gaa>Aaa p.E349K BLCA 19 57641253 57641253 + Missense_Mutation SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:57641253G>A c.1210G>A c.(1210-1212)Gaa>Aaa p.E404K BLCA 19 57641458 57641458 + Missense_Mutation SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr19:57641458C>A c.1415C>A c.(1414-1416)tCt>tAt p.S472Y BLCA 19 57641745 57641745 + Missense_Mutation SNP G G A TCGA-XF-AAN0-01A-11D-A42E-08 TCGA-XF-AAN0-10A-01D-A42H-08 g.chr19:57641745G>A c.1702G>A c.(1702-1704)Gag>Aag p.E568K BLCA 19 57641855 57641855 + Missense_Mutation SNP A A C TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr19:57641855A>C c.1812A>C c.(1810-1812)caA>caC p.Q604H BLCA 19 57641866 57641866 + Missense_Mutation SNP G G C TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr19:57641866G>C c.1823G>C c.(1822-1824)aGa>aCa p.R608T BLCA 19 57641934 57641934 + Missense_Mutation SNP G G C TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr19:57641934G>C c.1891G>C c.(1891-1893)Gaa>Caa p.E631Q BLCA 19 57641980 57641980 + Missense_Mutation SNP C C T TCGA-C4-A0EZ-01A-21D-A10S-08 TCGA-C4-A0EZ-10A-01D-A10S-08 g.chr19:57641980C>T c.1937C>T c.(1936-1938)cCa>cTa p.P646L BLCA 19 57642078 57642078 + Missense_Mutation SNP G G A TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr19:57642078G>A c.2035G>A c.(2035-2037)Gag>Aag p.E679K BLCA 19 57642258 57642258 + Missense_Mutation SNP G G C TCGA-UY-A78L-01A-12D-A339-08 TCGA-UY-A78L-10A-01D-A339-08 g.chr19:57642258G>C c.2215G>C c.(2215-2217)Gag>Cag p.E739Q BLCA 19 57642777 57642777 + Missense_Mutation SNP G G A TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr19:57642777G>A c.2734G>A c.(2734-2736)Gaa>Aaa p.E912K BRCA 19 57640254 57640254 + Missense_Mutation SNP C C T TCGA-A8-A08Z-01A-21W-A019-09 TCGA-A8-A08Z-10A-01W-A021-09 g.chr19:57640254C>T c.211C>T c.(211-213)Cac>Tac p.H71Y BRCA 19 57640371 57640371 + Missense_Mutation SNP C C T TCGA-E2-A14S-01A-11D-A12B-09 TCGA-E2-A14S-10A-01D-A12B-09 g.chr19:57640371C>T c.328C>T c.(328-330)Ccc>Tcc p.P110S BRCA 19 57640903 57640903 + Missense_Mutation SNP T T C TCGA-A2-A4S2-01A-12D-A25Q-09 TCGA-A2-A4S2-10A-01D-A25Q-09 g.chr19:57640903T>C c.860T>C c.(859-861)tTc>tCc p.F287S BRCA 19 57641241 57641241 + Nonsense_Mutation SNP G G T TCGA-EW-A1PH-01A-11D-A14K-09 TCGA-EW-A1PH-10A-01D-A14K-09 g.chr19:57641241G>T c.1198G>T c.(1198-1200)Gaa>Taa p.E400* BRCA 19 57641328 57641328 + Missense_Mutation SNP G G C TCGA-BH-A0B6-01A-11D-A19Y-09 TCGA-BH-A0B6-10A-01D-A19Y-09 g.chr19:57641328G>C c.1285G>C c.(1285-1287)Gag>Cag p.E429Q BRCA 19 57642432 57642432 + Missense_Mutation SNP A A C TCGA-AN-A0XN-01A-21D-A10G-09 TCGA-AN-A0XN-10A-01D-A10G-09 g.chr19:57642432A>C c.2389A>C c.(2389-2391)Att>Ctt p.I797L CESC 19 57640514 57640514 + Silent SNP G G C TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chr19:57640514G>C c.471G>C c.(469-471)gtG>gtC p.V157V CESC 19 57641166 57641166 + Nonsense_Mutation SNP G G T TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr19:57641166G>T c.1123G>T c.(1123-1125)Gag>Tag p.E375* CESC 19 57641463 57641463 + Missense_Mutation SNP G G C TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr19:57641463G>C c.1420G>C c.(1420-1422)Gat>Cat p.D474H CESC 19 57641624 57641624 + Missense_Mutation SNP G G T TCGA-C5-A2M2-01A-21D-A18J-09 TCGA-C5-A2M2-10A-01D-A18J-09 g.chr19:57641624G>T c.1581G>T c.(1579-1581)gaG>gaT p.E527D CESC 19 57641688 57641688 + Missense_Mutation SNP C C T TCGA-C5-A1BK-01B-11D-A13W-08 TCGA-C5-A1BK-10A-01D-A13W-08 g.chr19:57641688C>T c.1645C>T c.(1645-1647)Ctt>Ttt p.L549F CHOL 19 57641516 57641517 + Missense_Mutation DNP GA GA TC TCGA-3X-AAVC-01A-21D-A417-09 TCGA-3X-AAVC-10A-01D-A41A-09 g.chr19:57641516_57641517GA>TC c.1473_1474GA>TC c.(1471-1476)caGAag>caTCag p.491_492QK>HQ CHOL 19 57642416 57642416 + Missense_Mutation SNP C C A TCGA-3X-AAVC-01A-21D-A417-09 TCGA-3X-AAVC-10A-01D-A41A-09 g.chr19:57642416C>A c.2373C>A c.(2371-2373)aaC>aaA p.N791K COAD 19 57640117 57640117 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr19:57640117C>T c.74C>T c.(73-75)gCt>gTt p.A25V COAD 19 57640182 57640182 + Missense_Mutation SNP T T A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr19:57640182T>A c.139T>A c.(139-141)Ttt>Att p.F47I COAD 19 57640238 57640239 + Frame_Shift_Ins INS - - A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr19:57640238_57640239insA c.195_196insA c.(196-198)aaafs p.K66fs COAD 19 57640238 57640239 + Frame_Shift_Ins INS - - A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr19:57640238_57640239insA c.195_196insA c.(196-198)aaafs p.K66fs COAD 19 57640239 57640239 + Frame_Shift_Del DEL A A - TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr19:57640239delA c.196delA c.(196-198)aaafs p.K67fs COAD 19 57640239 57640239 + Frame_Shift_Del DEL A A - TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr19:57640239delA c.196delA c.(196-198)aaafs p.K67fs COAD 19 57640239 57640239 + Frame_Shift_Del DEL A A - TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr19:57640239delA c.196delA c.(196-198)aaafs p.K67fs COAD 19 57640286 57640286 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:57640286C>A c.243C>A c.(241-243)ttC>ttA p.F81L COAD 19 57640520 57640520 + Silent SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr19:57640520G>A c.477G>A c.(475-477)aaG>aaA p.K159K COAD 19 57640585 57640585 + Missense_Mutation SNP A A G TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr19:57640585A>G c.542A>G c.(541-543)gAg>gGg p.E181G COAD 19 57640713 57640713 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:57640713C>T c.670C>T c.(670-672)Ctc>Ttc p.L224F COAD 19 57640827 57640827 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr19:57640827C>T c.784C>T c.(784-786)Cac>Tac p.H262Y COAD 19 57640925 57640925 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr19:57640925T>G c.882T>G c.(880-882)tgT>tgG p.C294W COAD 19 57640930 57640930 + Missense_Mutation SNP T T G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr19:57640930T>G c.887T>G c.(886-888)aTg>aGg p.M296R COAD 19 57640949 57640949 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:57640949G>A c.906G>A c.(904-906)tcG>tcA p.S302S COAD 19 57641106 57641106 + Frame_Shift_Del DEL A A - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr19:57641106delA c.1063delA c.(1063-1065)aaafs p.K356fs COAD 19 57641404 57641404 + Missense_Mutation SNP T T C TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr19:57641404T>C c.1361T>C c.(1360-1362)cTc>cCc p.L454P COAD 19 57641534 57641534 + Silent SNP G G A TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr19:57641534G>A c.1491G>A c.(1489-1491)agG>agA p.R497R COAD 19 57641631 57641631 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr19:57641631T>G c.1588T>G c.(1588-1590)Tat>Gat p.Y530D COAD 19 57641649 57641649 + Missense_Mutation SNP A A G TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr19:57641649A>G c.1606A>G c.(1606-1608)Agt>Ggt p.S536G COAD 19 57641884 57641884 + Missense_Mutation SNP G G T TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr19:57641884G>T c.1841G>T c.(1840-1842)aGc>aTc p.S614I COAD 19 57641922 57641922 + Missense_Mutation SNP G G A TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr19:57641922G>A c.1879G>A c.(1879-1881)Gca>Aca p.A627T COAD 19 57641991 57641991 + Missense_Mutation SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr19:57641991T>C c.1948T>C c.(1948-1950)Tca>Cca p.S650P COAD 19 57642089 57642089 + Silent SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr19:57642089T>C c.2046T>C c.(2044-2046)ctT>ctC p.L682L COAD 19 57642199 57642199 + Missense_Mutation SNP A A G TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr19:57642199A>G c.2156A>G c.(2155-2157)aAa>aGa p.K719R COAD 19 57642200 57642200 + Silent SNP A A G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr19:57642200A>G c.2157A>G c.(2155-2157)aaA>aaG p.K719K COAD 19 57642593 57642593 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr19:57642593G>A c.2550G>A c.(2548-2550)aaG>aaA p.K850K COADREAD 19 57640117 57640117 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr19:57640117C>T c.74C>T c.(73-75)gCt>gTt p.A25V COADREAD 19 57640182 57640182 + Missense_Mutation SNP T T A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr19:57640182T>A c.139T>A c.(139-141)Ttt>Att p.F47I COADREAD 19 57640238 57640239 + Frame_Shift_Ins INS - - A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr19:57640238_57640239insA c.195_196insA c.(196-198)aaafs p.K66fs COADREAD 19 57640238 57640239 + Frame_Shift_Ins INS - - A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr19:57640238_57640239insA c.195_196insA c.(196-198)aaafs p.K66fs COADREAD 19 57640239 57640239 + Frame_Shift_Del DEL A A - TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr19:57640239delA c.196delA c.(196-198)aaafs p.K67fs COADREAD 19 57640239 57640239 + Frame_Shift_Del DEL A A - TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr19:57640239delA c.196delA c.(196-198)aaafs p.K67fs COADREAD 19 57640239 57640239 + Frame_Shift_Del DEL A A - TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr19:57640239delA c.196delA c.(196-198)aaafs p.K67fs COADREAD 19 57640286 57640286 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:57640286C>A c.243C>A c.(241-243)ttC>ttA p.F81L COADREAD 19 57640286 57640286 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr19:57640286C>A c.243C>A c.(241-243)ttC>ttA p.F81L COADREAD 19 57640520 57640520 + Silent SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr19:57640520G>A c.477G>A c.(475-477)aaG>aaA p.K159K COADREAD 19 57640585 57640585 + Missense_Mutation SNP A A G TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr19:57640585A>G c.542A>G c.(541-543)gAg>gGg p.E181G COADREAD 19 57640713 57640713 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:57640713C>T c.670C>T c.(670-672)Ctc>Ttc p.L224F COADREAD 19 57640827 57640827 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr19:57640827C>T c.784C>T c.(784-786)Cac>Tac p.H262Y COADREAD 19 57640913 57640913 + Missense_Mutation SNP G G T TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr19:57640913G>T c.870G>T c.(868-870)ttG>ttT p.L290F COADREAD 19 57640925 57640925 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr19:57640925T>G c.882T>G c.(880-882)tgT>tgG p.C294W COADREAD 19 57640930 57640930 + Missense_Mutation SNP T T G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr19:57640930T>G c.887T>G c.(886-888)aTg>aGg p.M296R COADREAD 19 57640949 57640949 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:57640949G>A c.906G>A c.(904-906)tcG>tcA p.S302S COADREAD 19 57641106 57641106 + Frame_Shift_Del DEL A A - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr19:57641106delA c.1063delA c.(1063-1065)aaafs p.K356fs COADREAD 19 57641161 57641161 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr19:57641161C>T c.1118C>T c.(1117-1119)gCt>gTt p.A373V COADREAD 19 57641404 57641404 + Missense_Mutation SNP T T C TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr19:57641404T>C c.1361T>C c.(1360-1362)cTc>cCc p.L454P COADREAD 19 57641404 57641404 + Missense_Mutation SNP T T C TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr19:57641404T>C c.1361T>C c.(1360-1362)cTc>cCc p.L454P COADREAD 19 57641534 57641534 + Silent SNP G G A TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr19:57641534G>A c.1491G>A c.(1489-1491)agG>agA p.R497R COADREAD 19 57641631 57641631 + Missense_Mutation SNP T T G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr19:57641631T>G c.1588T>G c.(1588-1590)Tat>Gat p.Y530D COADREAD 19 57641649 57641649 + Missense_Mutation SNP A A G TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr19:57641649A>G c.1606A>G c.(1606-1608)Agt>Ggt p.S536G COADREAD 19 57641702 57641702 + Silent SNP T T C TCGA-AF-3400-01A-01W-0831-10 TCGA-AF-3400-10A-01W-0831-10 g.chr19:57641702T>C c.1659T>C c.(1657-1659)agT>agC p.S553S COADREAD 19 57641759 57641759 + Missense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr19:57641759G>T c.1716G>T c.(1714-1716)gaG>gaT p.E572D COADREAD 19 57641884 57641884 + Missense_Mutation SNP G G T TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr19:57641884G>T c.1841G>T c.(1840-1842)aGc>aTc p.S614I COADREAD 19 57641922 57641922 + Missense_Mutation SNP G G A TCGA-AA-3543-01A-01W-0833-10 TCGA-AA-3543-10A-01W-0833-10 g.chr19:57641922G>A c.1879G>A c.(1879-1881)Gca>Aca p.A627T COADREAD 19 57641991 57641991 + Missense_Mutation SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr19:57641991T>C c.1948T>C c.(1948-1950)Tca>Cca p.S650P COADREAD 19 57642089 57642089 + Silent SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr19:57642089T>C c.2046T>C c.(2044-2046)ctT>ctC p.L682L COADREAD 19 57642199 57642199 + Missense_Mutation SNP A A G TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr19:57642199A>G c.2156A>G c.(2155-2157)aAa>aGa p.K719R COADREAD 19 57642200 57642200 + Silent SNP A A G TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr19:57642200A>G c.2157A>G c.(2155-2157)aaA>aaG p.K719K COADREAD 19 57642200 57642200 + Silent SNP A A G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr19:57642200A>G c.2157A>G c.(2155-2157)aaA>aaG p.K719K COADREAD 19 57642593 57642593 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr19:57642593G>A c.2550G>A c.(2548-2550)aaG>aaA p.K850K COADREAD 19 57642793 57642793 + Missense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr19:57642793C>A c.2750C>A c.(2749-2751)tCt>tAt p.S917Y DLBC 19 57640529 57640529 + Silent SNP A A G TCGA-FM-8000-01A-11D-2210-10 TCGA-FM-8000-10A-01D-2210-10 g.chr19:57640529A>G c.486A>G c.(484-486)ttA>ttG p.L162L DLBC 19 57641887 57641887 + Missense_Mutation SNP A A G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr19:57641887A>G c.1844A>G c.(1843-1845)cAa>cGa p.Q615R DLBC 19 57642413 57642413 + Missense_Mutation SNP C C A TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr19:57642413C>A c.2370C>A c.(2368-2370)gaC>gaA p.D790E ESCA 19 57640238 57640239 + Frame_Shift_Ins INS - - A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr19:57640238_57640239insA c.195_196insA c.(196-198)aaafs p.K66fs ESCA 19 57640428 57640428 + Missense_Mutation SNP A A C TCGA-JY-A93D-01A-11D-A387-09 TCGA-JY-A93D-10A-01D-A38A-09 g.chr19:57640428A>C c.385A>C c.(385-387)Att>Ctt p.I129L ESCA 19 57641629 57641629 + Missense_Mutation SNP T T G TCGA-L7-A6VZ-01A-12D-A33E-09 TCGA-L7-A6VZ-10A-01D-A33H-09 g.chr19:57641629T>G c.1586T>G c.(1585-1587)gTt>gGt p.V529G ESCA 19 57641839 57641839 + Missense_Mutation SNP A A C TCGA-R6-A6XG-01B-11D-A33E-09 TCGA-R6-A6XG-10A-01D-A33H-09 g.chr19:57641839A>C c.1796A>C c.(1795-1797)aAg>aCg p.K599T ESCA 19 57642310 57642310 + Missense_Mutation SNP G G A TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr19:57642310G>A c.2267G>A c.(2266-2268)aGg>aAg p.R756K GBM 19 57641232 57641232 + Missense_Mutation SNP A A G TCGA-19-2629-01A-01D-1495-08 TCGA-19-2629-10A-01D-1495-08 g.chr19:57641232A>G c.1189A>G c.(1189-1191)Act>Gct p.T397A GBM 19 57641754 57641754 + Missense_Mutation SNP T T A TCGA-14-0813-01A-01W-0424-08 TCGA-14-0813-10A-01W-0424-08 g.chr19:57641754T>A c.1711T>A c.(1711-1713)Tct>Act p.S571T GBMLGG 19 57641232 57641232 + Missense_Mutation SNP A A G TCGA-19-2629-01A-01D-1495-08 TCGA-19-2629-10A-01D-1495-08 g.chr19:57641232A>G c.1189A>G c.(1189-1191)Act>Gct p.T397A GBMLGG 19 57641354 57641354 + Silent SNP T T A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:57641354T>A c.1311T>A c.(1309-1311)atT>atA p.I437I GBMLGG 19 57641754 57641754 + Missense_Mutation SNP T T A TCGA-14-0813-01A-01W-0424-08 TCGA-14-0813-10A-01W-0424-08 g.chr19:57641754T>A c.1711T>A c.(1711-1713)Tct>Act p.S571T GBMLGG 19 57641872 57641872 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:57641872G>A c.1829G>A c.(1828-1830)tGt>tAt p.C610Y GBMLGG 19 57642572 57642572 + Silent SNP C C T TCGA-QH-A6XC-01A-12D-A32B-08 TCGA-QH-A6XC-10B-01D-A329-08 g.chr19:57642572C>T c.2529C>T c.(2527-2529)agC>agT p.S843S HNSC 19 57640091 57640091 + Missense_Mutation SNP G G T TCGA-CQ-6223-01A-11D-1912-08 TCGA-CQ-6223-10A-01D-1912-08 g.chr19:57640091G>T c.48G>T c.(46-48)aaG>aaT p.K16N HNSC 19 57640145 57640145 + Silent SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr19:57640145G>A c.102G>A c.(100-102)aaG>aaA p.K34K HNSC 19 57640564 57640564 + Nonsense_Mutation SNP C C A TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr19:57640564C>A c.521C>A c.(520-522)tCa>tAa p.S174* HNSC 19 57640633 57640633 + Missense_Mutation SNP C C T TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr19:57640633C>T c.590C>T c.(589-591)aCa>aTa p.T197I HNSC 19 57640702 57640702 + Missense_Mutation SNP G G C TCGA-T3-A92M-01A-31D-A391-08 TCGA-T3-A92M-10A-01D-A394-08 g.chr19:57640702G>C c.659G>C c.(658-660)aGa>aCa p.R220T HNSC 19 57640887 57640887 + Missense_Mutation SNP C C A TCGA-HD-A6I0-01A-11D-A31L-08 TCGA-HD-A6I0-10A-01D-A31J-08 g.chr19:57640887C>A c.844C>A c.(844-846)Caa>Aaa p.Q282K HNSC 19 57640945 57640945 + Missense_Mutation SNP A A C TCGA-CQ-6218-01A-11D-1912-08 TCGA-CQ-6218-10A-01D-1912-08 g.chr19:57640945A>C c.902A>C c.(901-903)cAa>cCa p.Q301P HNSC 19 57641043 57641043 + Missense_Mutation SNP C C A TCGA-CN-5359-01A-01D-1434-08 TCGA-CN-5359-10A-01D-1434-08 g.chr19:57641043C>A c.1000C>A c.(1000-1002)Cag>Aag p.Q334K HNSC 19 57641576 57641576 + Silent SNP G G A TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr19:57641576G>A c.1533G>A c.(1531-1533)ctG>ctA p.L511L HNSC 19 57641686 57641686 + Missense_Mutation SNP C C T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr19:57641686C>T c.1643C>T c.(1642-1644)cCt>cTt p.P548L HNSC 19 57641701 57641701 + Missense_Mutation SNP G G T TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr19:57641701G>T c.1658G>T c.(1657-1659)aGt>aTt p.S553I HNSC 19 57641738 57641738 + Silent SNP C C A TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr19:57641738C>A c.1695C>A c.(1693-1695)gtC>gtA p.V565V HNSC 19 57641804 57641804 + Silent SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr19:57641804C>T c.1761C>T c.(1759-1761)tcC>tcT p.S587S HNSC 19 57641807 57641807 + Missense_Mutation SNP T T A TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chr19:57641807T>A c.1764T>A c.(1762-1764)agT>agA p.S588R HNSC 19 57641825 57641825 + Silent SNP C C A TCGA-UF-A71A-01A-22D-A34J-08 TCGA-UF-A71A-10A-01D-A34M-08 g.chr19:57641825C>A c.1782C>A c.(1780-1782)ccC>ccA p.P594P HNSC 19 57641829 57641829 + Nonsense_Mutation SNP G G T TCGA-CN-5360-01A-01D-1434-08 TCGA-CN-5360-10A-01D-1434-08 g.chr19:57641829G>T c.1786G>T c.(1786-1788)Gaa>Taa p.E596* HNSC 19 57641988 57641988 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr19:57641988G>A c.1945G>A c.(1945-1947)Gac>Aac p.D649N HNSC 19 57642105 57642105 + Missense_Mutation SNP C C A TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr19:57642105C>A c.2062C>A c.(2062-2064)Cat>Aat p.H688N HNSC 19 57642147 57642147 + Missense_Mutation SNP G G C TCGA-CV-7411-01A-11D-2078-08 TCGA-CV-7411-10A-01D-2078-08 g.chr19:57642147G>C c.2104G>C c.(2104-2106)Gag>Cag p.E702Q HNSC 19 57642321 57642321 + Missense_Mutation SNP G G T TCGA-BA-A4IH-01A-11D-A25Y-08 TCGA-BA-A4IH-10A-01D-A25Y-08 g.chr19:57642321G>T c.2278G>T c.(2278-2280)Gcc>Tcc p.A760S HNSC 19 57642360 57642360 + Missense_Mutation SNP G G A TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr19:57642360G>A c.2317G>A c.(2317-2319)Gaa>Aaa p.E773K HNSC 19 57642405 57642405 + Missense_Mutation SNP G G T TCGA-CV-6953-01A-11D-1912-08 TCGA-CV-6953-10A-01D-1912-08 g.chr19:57642405G>T c.2362G>T c.(2362-2364)Ggt>Tgt p.G788C KICH 19 57641826 57641826 + Missense_Mutation SNP G G A TCGA-KN-8418-01A-11D-2310-10 TCGA-KN-8418-11A-01D-2310-10 g.chr19:57641826G>A c.1783G>A c.(1783-1785)Gtt>Att p.V595I KIPAN 19 57640818 57640818 + Nonsense_Mutation SNP G G T TCGA-B0-5107-01A-01D-1421-08 TCGA-B0-5107-11A-01D-1421-08 g.chr19:57640818G>T c.775G>T c.(775-777)Gaa>Taa p.E259* KIPAN 19 57640983 57640984 + Missense_Mutation DNP CT CT AA TCGA-5P-A9JU-01A-11D-A42J-10 TCGA-5P-A9JU-10A-01D-A42M-10 g.chr19:57640983_57640984CT>AA c.940_941CT>AA c.(940-942)CTc>AAc p.L314N KIPAN 19 57641187 57641187 + Missense_Mutation SNP G G C TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr19:57641187G>C c.1144G>C c.(1144-1146)Gac>Cac p.D382H KIPAN 19 57641826 57641826 + Missense_Mutation SNP G G A TCGA-KN-8418-01A-11D-2310-10 TCGA-KN-8418-11A-01D-2310-10 g.chr19:57641826G>A c.1783G>A c.(1783-1785)Gtt>Att p.V595I KIPAN 19 57642200 57642200 + Silent SNP A A G TCGA-Y8-A8RZ-01A-11D-A36X-10 TCGA-Y8-A8RZ-10A-01D-A370-10 g.chr19:57642200A>G c.2157A>G c.(2155-2157)aaA>aaG p.K719K KIPAN 19 57642541 57642541 + Missense_Mutation SNP G G A TCGA-CZ-5461-01A-01D-1501-10 TCGA-CZ-5461-11A-01D-1501-10 g.chr19:57642541G>A c.2498G>A c.(2497-2499)gGg>gAg p.G833E KIPAN 19 57642738 57642739 + Missense_Mutation DNP CG CG AT TCGA-B0-5705-01A-11D-1534-10 TCGA-B0-5705-11A-01D-1534-10 g.chr19:57642738_57642739CG>AT c.2695_2696CG>AT c.(2695-2697)CGg>ATg p.R899M KIPAN 19 57642746 57642746 + Silent SNP T T C TCGA-B0-5705-01A-11D-1534-10 TCGA-B0-5705-11A-01D-1534-10 g.chr19:57642746T>C c.2703T>C c.(2701-2703)ccT>ccC p.P901P KIRC 19 57640818 57640818 + Nonsense_Mutation SNP G G T TCGA-B0-5107-01A-01D-1421-08 TCGA-B0-5107-11A-01D-1421-08 g.chr19:57640818G>T c.775G>T c.(775-777)Gaa>Taa p.E259* KIRC 19 57642541 57642541 + Missense_Mutation SNP G G A TCGA-CZ-5461-01A-01D-1501-10 TCGA-CZ-5461-11A-01D-1501-10 g.chr19:57642541G>A c.2498G>A c.(2497-2499)gGg>gAg p.G833E KIRC 19 57642738 57642739 + Missense_Mutation DNP CG CG AT TCGA-B0-5705-01A-11D-1534-10 TCGA-B0-5705-11A-01D-1534-10 g.chr19:57642738_57642739CG>AT c.2695_2696CG>AT c.(2695-2697)CGg>ATg p.R899M KIRC 19 57642746 57642746 + Silent SNP T T C TCGA-B0-5705-01A-11D-1534-10 TCGA-B0-5705-11A-01D-1534-10 g.chr19:57642746T>C c.2703T>C c.(2701-2703)ccT>ccC p.P901P KIRP 19 57640983 57640984 + Missense_Mutation DNP CT CT AA TCGA-5P-A9JU-01A-11D-A42J-10 TCGA-5P-A9JU-10A-01D-A42M-10 g.chr19:57640983_57640984CT>AA c.940_941CT>AA c.(940-942)CTc>AAc p.L314N KIRP 19 57641187 57641187 + Missense_Mutation SNP G G C TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr19:57641187G>C c.1144G>C c.(1144-1146)Gac>Cac p.D382H KIRP 19 57642200 57642200 + Silent SNP A A G TCGA-Y8-A8RZ-01A-11D-A36X-10 TCGA-Y8-A8RZ-10A-01D-A370-10 g.chr19:57642200A>G c.2157A>G c.(2155-2157)aaA>aaG p.K719K LGG 19 57641354 57641354 + Silent SNP T T A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:57641354T>A c.1311T>A c.(1309-1311)atT>atA p.I437I LGG 19 57641872 57641872 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:57641872G>A c.1829G>A c.(1828-1830)tGt>tAt p.C610Y LGG 19 57642572 57642572 + Silent SNP C C T TCGA-QH-A6XC-01A-12D-A32B-08 TCGA-QH-A6XC-10B-01D-A329-08 g.chr19:57642572C>T c.2529C>T c.(2527-2529)agC>agT p.S843S LIHC 19 57640050 57640050 + Missense_Mutation SNP T T A TCGA-G3-A3CI-01A-11D-A20W-10 TCGA-G3-A3CI-10A-01D-A20W-10 g.chr19:57640050T>A c.7T>A c.(7-9)Tct>Act p.S3T LIHC 19 57641581 57641581 + Missense_Mutation SNP G G T TCGA-G3-AAV2-01A-11D-A36X-10 TCGA-G3-AAV2-10A-01D-A370-10 g.chr19:57641581G>T c.1538G>T c.(1537-1539)cGc>cTc p.R513L LIHC 19 57641665 57641665 + Missense_Mutation SNP G G A TCGA-2V-A95S-01A-11D-A36X-10 TCGA-2V-A95S-10D-01D-A370-10 g.chr19:57641665G>A c.1622G>A c.(1621-1623)tGc>tAc p.C541Y LUAD 19 57640047 57640047 + Missense_Mutation SNP A A T TCGA-73-4658-01A-01D-1753-08 TCGA-73-4658-11A-01D-1753-08 g.chr19:57640047A>T c.4A>T c.(4-6)Ata>Tta p.I2L LUAD 19 57640155 57640155 + Missense_Mutation SNP C C A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr19:57640155C>A c.112C>A c.(112-114)Ctg>Atg p.L38M LUAD 19 57640187 57640187 + Silent SNP A A T TCGA-17-Z023-01A-01W-0746-08 TCGA-17-Z023-11A-01W-0746-08 g.chr19:57640187A>T c.144A>T c.(142-144)atA>atT p.I48I LUAD 19 57640201 57640201 + Missense_Mutation SNP T T A TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr19:57640201T>A c.158T>A c.(157-159)cTg>cAg p.L53Q LUAD 19 57640238 57640239 + Frame_Shift_Ins INS - - A TCGA-97-8175-01A-11D-2284-08 TCGA-97-8175-10A-01D-2284-08 g.chr19:57640238_57640239insA c.195_196insA c.(196-198)aaafs p.K66fs LUAD 19 57640279 57640279 + Missense_Mutation SNP A A T TCGA-53-7626-01A-12D-2063-08 TCGA-53-7626-10A-01D-2063-08 g.chr19:57640279A>T c.236A>T c.(235-237)aAc>aTc p.N79I LUAD 19 57640280 57640280 + Missense_Mutation SNP C C A TCGA-49-6767-01A-11D-1855-08 TCGA-49-6767-11A-01D-1855-08 g.chr19:57640280C>A c.237C>A c.(235-237)aaC>aaA p.N79K LUAD 19 57640389 57640389 + Missense_Mutation SNP G G T TCGA-44-A47B-01A-11D-A24D-08 TCGA-44-A47B-10A-01D-A24F-08 g.chr19:57640389G>T c.346G>T c.(346-348)Gat>Tat p.D116Y LUAD 19 57640419 57640419 + Missense_Mutation SNP C C A TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr19:57640419C>A c.376C>A c.(376-378)Ctg>Atg p.L126M LUAD 19 57640451 57640451 + Missense_Mutation SNP C C A TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr19:57640451C>A c.408C>A c.(406-408)agC>agA p.S136R LUAD 19 57640595 57640595 + Silent SNP G G T TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr19:57640595G>T c.552G>T c.(550-552)ctG>ctT p.L184L LUAD 19 57640599 57640599 + Nonsense_Mutation SNP G G T TCGA-97-A4M5-01A-11D-A24P-08 TCGA-97-A4M5-10A-01D-A24P-08 g.chr19:57640599G>T c.556G>T c.(556-558)Gaa>Taa p.E186* LUAD 19 57640629 57640629 + Missense_Mutation SNP A A G TCGA-50-5931-01A-11D-1753-08 TCGA-50-5931-11A-01D-1753-08 g.chr19:57640629A>G c.586A>G c.(586-588)Aag>Gag p.K196E LUAD 19 57640629 57640629 + Nonsense_Mutation SNP A A T TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr19:57640629A>T c.586A>T c.(586-588)Aag>Tag p.K196* LUAD 19 57640645 57640645 + Missense_Mutation SNP A A G TCGA-17-Z044-01A-01W-0746-08 TCGA-17-Z044-11A-01W-0746-08 g.chr19:57640645A>G c.602A>G c.(601-603)aAa>aGa p.K201R LUAD 19 57640670 57640670 + Missense_Mutation SNP C C G TCGA-78-7154-01A-11D-2036-08 TCGA-78-7154-10A-01D-2036-08 g.chr19:57640670C>G c.627C>G c.(625-627)aaC>aaG p.N209K LUAD 19 57640672 57640672 + Missense_Mutation SNP C C A TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr19:57640672C>A c.629C>A c.(628-630)cCa>cAa p.P210Q LUAD 19 57640737 57640738 + Frame_Shift_Ins INS - - C TCGA-78-7537-01A-11D-2063-08 TCGA-78-7537-10A-01D-2063-08 g.chr19:57640737_57640738insC c.694_695insC c.(694-696)tgtfs p.C232fs LUAD 19 57640799 57640799 + Silent SNP T T C TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr19:57640799T>C c.756T>C c.(754-756)aaT>aaC p.N252N LUAD 19 57640890 57640890 + Missense_Mutation SNP C C A TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chr19:57640890C>A c.847C>A c.(847-849)Ctg>Atg p.L283M LUAD 19 57640928 57640928 + Nonsense_Mutation SNP C C A TCGA-38-4629-01A-02D-1265-08 TCGA-38-4629-11A-01D-1265-08 g.chr19:57640928C>A c.885C>A c.(883-885)taC>taA p.Y295* LUAD 19 57641161 57641161 + Missense_Mutation SNP C C A TCGA-05-4405-01A-21D-1855-08 TCGA-05-4405-10A-01D-1855-08 g.chr19:57641161C>A c.1118C>A c.(1117-1119)gCt>gAt p.A373D LUAD 19 57641213 57641213 + Missense_Mutation SNP A A C TCGA-05-4405-01A-21D-1855-08 TCGA-05-4405-10A-01D-1855-08 g.chr19:57641213A>C c.1170A>C c.(1168-1170)aaA>aaC p.K390N LUAD 19 57641309 57641309 + Nonsense_Mutation SNP C C A TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr19:57641309C>A c.1266C>A c.(1264-1266)tgC>tgA p.C422* LUAD 19 57641310 57641310 + Missense_Mutation SNP C C A TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr19:57641310C>A c.1267C>A c.(1267-1269)Cct>Act p.P423T LUAD 19 57641420 57641420 + Silent SNP C C T TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chr19:57641420C>T c.1377C>T c.(1375-1377)caC>caT p.H459H LUAD 19 57641436 57641436 + Missense_Mutation SNP C C A TCGA-17-Z062-01A-01W-0747-08 TCGA-17-Z062-11A-01W-0747-08 g.chr19:57641436C>A c.1393C>A c.(1393-1395)Ctt>Att p.L465I LUAD 19 57641439 57641439 + Missense_Mutation SNP C C A TCGA-55-6987-01A-11D-1945-08 TCGA-55-6987-11A-01D-1945-08 g.chr19:57641439C>A c.1396C>A c.(1396-1398)Cct>Act p.P466T LUAD 19 57641440 57641440 + Missense_Mutation SNP C C A TCGA-55-6987-01A-11D-1945-08 TCGA-55-6987-11A-01D-1945-08 g.chr19:57641440C>A c.1397C>A c.(1396-1398)cCt>cAt p.P466H LUAD 19 57641606 57641606 + Missense_Mutation SNP G G T TCGA-73-7498-01A-12D-2184-08 TCGA-73-7498-10A-01D-2184-08 g.chr19:57641606G>T c.1563G>T c.(1561-1563)ttG>ttT p.L521F LUAD 19 57641649 57641649 + Missense_Mutation SNP A A G TCGA-44-6774-01A-21D-1855-08 TCGA-44-6774-10A-01D-1855-08 g.chr19:57641649A>G c.1606A>G c.(1606-1608)Agt>Ggt p.S536G LUAD 19 57641688 57641688 + Missense_Mutation SNP C C G TCGA-17-Z062-01A-01W-0747-08 TCGA-17-Z062-11A-01W-0747-08 g.chr19:57641688C>G c.1645C>G c.(1645-1647)Ctt>Gtt p.L549V LUAD 19 57641790 57641790 + Missense_Mutation SNP C C A TCGA-44-4112-01A-01D-1105-08 TCGA-44-4112-10A-01D-1458-08 g.chr19:57641790C>A c.1747C>A c.(1747-1749)Ctg>Atg p.L583M LUAD 19 57641898 57641898 + Missense_Mutation SNP C C A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr19:57641898C>A c.1855C>A c.(1855-1857)Cag>Aag p.Q619K LUAD 19 57642003 57642003 + Missense_Mutation SNP C C A TCGA-44-A479-01A-31D-A24D-08 TCGA-44-A479-10A-01D-A24F-08 g.chr19:57642003C>A c.1960C>A c.(1960-1962)Cag>Aag p.Q654K LUAD 19 57642009 57642009 + Missense_Mutation SNP G G T TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr19:57642009G>T c.1966G>T c.(1966-1968)Gac>Tac p.D656Y LUAD 19 57642047 57642047 + Missense_Mutation SNP G G T TCGA-62-A46S-01A-11D-A24D-08 TCGA-62-A46S-10A-01D-A24F-08 g.chr19:57642047G>T c.2004G>T c.(2002-2004)aaG>aaT p.K668N LUAD 19 57642109 57642109 + Missense_Mutation SNP C C A TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chr19:57642109C>A c.2066C>A c.(2065-2067)cCa>cAa p.P689Q LUAD 19 57642177 57642177 + Missense_Mutation SNP A A G TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr19:57642177A>G c.2134A>G c.(2134-2136)Acc>Gcc p.T712A LUAD 19 57642182 57642182 + Silent SNP T T C TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr19:57642182T>C c.2139T>C c.(2137-2139)aaT>aaC p.N713N LUAD 19 57642250 57642250 + Missense_Mutation SNP A A T TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chr19:57642250A>T c.2207A>T c.(2206-2208)cAg>cTg p.Q736L LUAD 19 57642466 57642466 + Missense_Mutation SNP A A T TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chr19:57642466A>T c.2423A>T c.(2422-2424)aAg>aTg p.K808M LUAD 19 57642509 57642509 + Silent SNP C C A TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr19:57642509C>A c.2466C>A c.(2464-2466)gcC>gcA p.A822A LUAD 19 57642596 57642596 + Missense_Mutation SNP G G T TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr19:57642596G>T c.2553G>T c.(2551-2553)caG>caT p.Q851H LUAD 19 57642636 57642636 + Missense_Mutation SNP T T A TCGA-75-6211-01A-11D-1753-08 TCGA-75-6211-10A-01D-1753-08 g.chr19:57642636T>A c.2593T>A c.(2593-2595)Tca>Aca p.S865T LUAD 19 57642670 57642670 + Missense_Mutation SNP C C T TCGA-53-A4EZ-01A-12D-A24P-08 TCGA-53-A4EZ-10A-01D-A24P-08 g.chr19:57642670C>T c.2627C>T c.(2626-2628)tCt>tTt p.S876F LUAD 19 57642760 57642760 + Missense_Mutation SNP G G T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr19:57642760G>T c.2717G>T c.(2716-2718)gGg>gTg p.G906V LUAD 19 57642761 57642761 + Silent SNP G G T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr19:57642761G>T c.2718G>T c.(2716-2718)ggG>ggT p.G906G LUSC 19 57640074 57640074 + Nonsense_Mutation SNP C C T TCGA-39-5027-01A-21D-1817-08 TCGA-39-5027-11A-01D-1817-08 g.chr19:57640074C>T c.31C>T c.(31-33)Caa>Taa p.Q11* LUSC 19 57640084 57640084 + Missense_Mutation SNP G G A TCGA-39-5027-01A-21D-1817-08 TCGA-39-5027-11A-01D-1817-08 g.chr19:57640084G>A c.41G>A c.(40-42)aGc>aAc p.S14N LUSC 19 57640100 57640100 + Missense_Mutation SNP G G C TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chr19:57640100G>C c.57G>C c.(55-57)atG>atC p.M19I LUSC 19 57640252 57640252 + Missense_Mutation SNP G G T TCGA-60-2725-01A-01D-1267-08 TCGA-60-2725-11A-01D-1267-08 g.chr19:57640252G>T c.209G>T c.(208-210)aGt>aTt p.S70I LUSC 19 57640425 57640425 + Nonsense_Mutation SNP G G T TCGA-51-4079-01A-01D-1458-08 TCGA-51-4079-11A-01D-1458-08 g.chr19:57640425G>T c.382G>T c.(382-384)Gaa>Taa p.E128* LUSC 19 57640572 57640572 + Missense_Mutation SNP G G T TCGA-51-4081-01A-01D-1458-08 TCGA-51-4081-11A-01D-1458-08 g.chr19:57640572G>T c.529G>T c.(529-531)Gta>Tta p.V177L LUSC 19 57640619 57640619 + Missense_Mutation SNP C C G TCGA-60-2721-01A-01D-1522-08 TCGA-60-2721-11A-01D-1522-08 g.chr19:57640619C>G c.576C>G c.(574-576)aaC>aaG p.N192K LUSC 19 57640692 57640692 + Missense_Mutation SNP G G C TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr19:57640692G>C c.649G>C c.(649-651)Gaa>Caa p.E217Q LUSC 19 57640894 57640894 + Missense_Mutation SNP A A T TCGA-66-2768-01A-01D-1522-08 TCGA-66-2768-11A-01D-1522-08 g.chr19:57640894A>T c.851A>T c.(850-852)cAg>cTg p.Q284L LUSC 19 57640914 57640914 + Missense_Mutation SNP G G A TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr19:57640914G>A c.871G>A c.(871-873)Gga>Aga p.G291R LUSC 19 57641067 57641067 + Missense_Mutation SNP T T C TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr19:57641067T>C c.1024T>C c.(1024-1026)Tgt>Cgt p.C342R LUSC 19 57641313 57641313 + Missense_Mutation SNP G G T TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr19:57641313G>T c.1270G>T c.(1270-1272)Gtt>Ttt p.V424F LUSC 19 57641512 57641512 + Missense_Mutation SNP A A C TCGA-46-3765-01A-01D-0983-08 TCGA-46-3765-10A-01D-0983-08 g.chr19:57641512A>C c.1469A>C c.(1468-1470)aAg>aCg p.K490T LUSC 19 57641900 57641900 + Missense_Mutation SNP G G C TCGA-60-2708-01A-01D-1522-08 TCGA-60-2708-11A-01D-1522-08 g.chr19:57641900G>C c.1857G>C c.(1855-1857)caG>caC p.Q619H LUSC 19 57642468 57642468 + Nonsense_Mutation SNP G G T TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr19:57642468G>T c.2425G>T c.(2425-2427)Gaa>Taa p.E809* LUSC 19 57642683 57642683 + Silent SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr19:57642683C>T c.2640C>T c.(2638-2640)ttC>ttT p.F880F LUSC 19 57642748 57642748 + Missense_Mutation SNP G G C TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr19:57642748G>C c.2705G>C c.(2704-2706)aGc>aCc p.S902T LUSC 19 57642755 57642755 + Missense_Mutation SNP G G T TCGA-66-2791-01A-01D-0983-08 TCGA-66-2791-11A-01D-0983-08 g.chr19:57642755G>T c.2712G>T c.(2710-2712)caG>caT p.Q904H OV 19 57640847 57640847 + Silent SNP A A G TCGA-13-2059-01A-01D-1526-09 TCGA-13-2059-10A-01D-1526-09 g.chr19:57640847A>G c.804A>G c.(802-804)agA>agG p.R268R OV 19 57640874 57640874 + Missense_Mutation SNP C C A TCGA-13-1484-01A-01W-0545-08 TCGA-13-1484-10A-01W-0545-08 g.chr19:57640874C>A c.831C>A c.(829-831)gaC>gaA p.D277E OV 19 57641014 57641014 + Missense_Mutation SNP C C G TCGA-24-1847-01A-01W-0633-09 TCGA-24-1847-10A-01W-0634-09 g.chr19:57641014C>G c.971C>G c.(970-972)cCc>cGc p.P324R OV 19 57641099 57641099 + Silent SNP G G A TCGA-61-1900-01A-01W-0639-09 TCGA-61-1900-11A-01W-0640-09 g.chr19:57641099G>A c.1056G>A c.(1054-1056)ggG>ggA p.G352G OV 19 57642198 57642198 + Nonsense_Mutation SNP A A T TCGA-10-0931-01A-01W-0420-08 TCGA-10-0931-11A-01W-0420-08 g.chr19:57642198A>T c.2155A>T c.(2155-2157)Aaa>Taa p.K719* PAAD 19 57641566 57641566 + Missense_Mutation SNP T T A TCGA-XD-AAUI-01A-42D-A40W-08 TCGA-XD-AAUI-10A-01D-A40W-08 g.chr19:57641566T>A c.1523T>A c.(1522-1524)aTc>aAc p.I508N PAAD 19 57642144 57642144 + Missense_Mutation SNP G G A TCGA-FB-AAPP-01A-12D-A40W-08 TCGA-FB-AAPP-11A-11D-A40W-08 g.chr19:57642144G>A c.2101G>A c.(2101-2103)Gta>Ata p.V701I PRAD 19 57640482 57640482 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:57640482C>T c.439C>T c.(439-441)Cct>Tct p.P147S PRAD 19 57640708 57640708 + Missense_Mutation SNP T T C TCGA-EJ-5507-01A-01D-1576-08 TCGA-EJ-5507-10A-01D-1577-08 g.chr19:57640708T>C c.665T>C c.(664-666)tTg>tCg p.L222S PRAD 19 57641660 57641660 + Silent SNP T T G TCGA-M7-A723-01A-12D-A32B-08 TCGA-M7-A723-10A-01D-A329-08 g.chr19:57641660T>G c.1617T>G c.(1615-1617)tcT>tcG p.S539S PRAD 19 57642355 57642355 + Missense_Mutation SNP C C A TCGA-ZG-A9N3-01A-11D-A41K-08 TCGA-ZG-A9N3-10A-01D-A41N-08 g.chr19:57642355C>A c.2312C>A c.(2311-2313)tCt>tAt p.S771Y READ 19 57640286 57640286 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr19:57640286C>A c.243C>A c.(241-243)ttC>ttA p.F81L READ 19 57640913 57640913 + Missense_Mutation SNP G G T TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr19:57640913G>T c.870G>T c.(868-870)ttG>ttT p.L290F READ 19 57641161 57641161 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr19:57641161C>T c.1118C>T c.(1117-1119)gCt>gTt p.A373V READ 19 57641404 57641404 + Missense_Mutation SNP T T C TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr19:57641404T>C c.1361T>C c.(1360-1362)cTc>cCc p.L454P READ 19 57641702 57641702 + Silent SNP T T C TCGA-AF-3400-01A-01W-0831-10 TCGA-AF-3400-10A-01W-0831-10 g.chr19:57641702T>C c.1659T>C c.(1657-1659)agT>agC p.S553S READ 19 57641759 57641759 + Missense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr19:57641759G>T c.1716G>T c.(1714-1716)gaG>gaT p.E572D READ 19 57642200 57642200 + Silent SNP A A G TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr19:57642200A>G c.2157A>G c.(2155-2157)aaA>aaG p.K719K READ 19 57642793 57642793 + Missense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr19:57642793C>A c.2750C>A c.(2749-2751)tCt>tAt p.S917Y SKCM 19 57640051 57640051 + Missense_Mutation SNP C C T TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr19:57640051C>T c.8C>T c.(7-9)tCt>tTt p.S3F SKCM 19 57640096 57640096 + Missense_Mutation SNP G G A TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr19:57640096G>A c.53G>A c.(52-54)gGg>gAg p.G18E SKCM 19 57640177 57640177 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr19:57640177G>A c.134G>A c.(133-135)gGa>gAa p.G45E SKCM 19 57640194 57640194 + Missense_Mutation SNP T T C TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr19:57640194T>C c.151T>C c.(151-153)Ttt>Ctt p.F51L SKCM 19 57640197 57640197 + Nonsense_Mutation SNP C C T TCGA-EE-A2MH-06A-11D-A197-08 TCGA-EE-A2MH-10A-01D-A199-08 g.chr19:57640197C>T c.154C>T c.(154-156)Cag>Tag p.Q52* SKCM 19 57640197 57640197 + Nonsense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr19:57640197C>T c.154C>T c.(154-156)Cag>Tag p.Q52* SKCM 19 57640306 57640306 + Missense_Mutation SNP C C T TCGA-EE-A2M6-06A-12D-A197-08 TCGA-EE-A2M6-10A-01D-A199-08 g.chr19:57640306C>T c.263C>T c.(262-264)tCc>tTc p.S88F SKCM 19 57640373 57640373 + Silent SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr19:57640373C>T c.330C>T c.(328-330)ccC>ccT p.P110P SKCM 19 57640376 57640376 + Missense_Mutation SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr19:57640376G>A c.333G>A c.(331-333)atG>atA p.M111I SKCM 19 57640381 57640381 + Missense_Mutation SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr19:57640381C>T c.338C>T c.(337-339)tCt>tTt p.S113F SKCM 19 57640386 57640386 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:57640386G>A c.343G>A c.(343-345)Gat>Aat p.D115N SKCM 19 57640389 57640389 + Missense_Mutation SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr19:57640389G>A c.346G>A c.(346-348)Gat>Aat p.D116N SKCM 19 57640389 57640389 + Missense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr19:57640389G>A c.346G>A c.(346-348)Gat>Aat p.D116N SKCM 19 57640452 57640452 + Missense_Mutation SNP A A G TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr19:57640452A>G c.409A>G c.(409-411)Att>Gtt p.I137V SKCM 19 57640501 57640501 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr19:57640501C>T c.458C>T c.(457-459)tCa>tTa p.S153L SKCM 19 57640501 57640501 + Missense_Mutation SNP C C T TCGA-EE-A3JH-06A-11D-A21A-08 TCGA-EE-A3JH-10A-01D-A21A-08 g.chr19:57640501C>T c.458C>T c.(457-459)tCa>tTa p.S153L SKCM 19 57640539 57640539 + Missense_Mutation SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr19:57640539G>A c.496G>A c.(496-498)Ggt>Agt p.G166S SKCM 19 57640569 57640569 + Missense_Mutation SNP G G A TCGA-EE-A2GU-06A-11D-A196-08 TCGA-EE-A2GU-10A-01D-A198-08 g.chr19:57640569G>A c.526G>A c.(526-528)Gat>Aat p.D176N SKCM 19 57640685 57640685 + Silent SNP G G A TCGA-FR-A3YO-06A-11D-A23B-08 TCGA-FR-A3YO-10A-01D-A23B-08 g.chr19:57640685G>A c.642G>A c.(640-642)gaG>gaA p.E214E SKCM 19 57640713 57640713 + Missense_Mutation SNP C C T TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr19:57640713C>T c.670C>T c.(670-672)Ctc>Ttc p.L224F SKCM 19 57640749 57640749 + Missense_Mutation SNP C C T TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chr19:57640749C>T c.706C>T c.(706-708)Cct>Tct p.P236S SKCM 19 57640749 57640749 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr19:57640749C>T c.706C>T c.(706-708)Cct>Tct p.P236S SKCM 19 57640800 57640800 + Missense_Mutation SNP G G A TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr19:57640800G>A c.757G>A c.(757-759)Ggt>Agt p.G253S SKCM 19 57640915 57640915 + Missense_Mutation SNP G G A TCGA-EE-A29N-06A-12D-A197-08 TCGA-EE-A29N-10A-01D-A199-08 g.chr19:57640915G>A c.872G>A c.(871-873)gGa>gAa p.G291E SKCM 19 57640915 57640915 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr19:57640915G>A c.872G>A c.(871-873)gGa>gAa p.G291E SKCM 19 57640915 57640915 + Missense_Mutation SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr19:57640915G>A c.872G>A c.(871-873)gGa>gAa p.G291E SKCM 19 57640948 57640948 + Missense_Mutation SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr19:57640948C>T c.905C>T c.(904-906)tCg>tTg p.S302L SKCM 19 57640962 57640962 + Missense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr19:57640962C>T c.919C>T c.(919-921)Cca>Tca p.P307S SKCM 19 57640963 57640963 + Missense_Mutation SNP C C T TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr19:57640963C>T c.920C>T c.(919-921)cCa>cTa p.P307L SKCM 19 57640966 57640966 + Missense_Mutation SNP C C T TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr19:57640966C>T c.923C>T c.(922-924)tCt>tTt p.S308F SKCM 19 57640991 57640991 + Missense_Mutation SNP A A C TCGA-D3-A2JL-06A-11D-A196-08 TCGA-D3-A2JL-10A-01D-A198-08 g.chr19:57640991A>C c.948A>C c.(946-948)caA>caC p.Q316H SKCM 19 57640998 57640998 + Missense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr19:57640998C>T c.955C>T c.(955-957)Cca>Tca p.P319S SKCM 19 57641002 57641002 + Nonsense_Mutation SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr19:57641002G>A c.959G>A c.(958-960)tGg>tAg p.W320* SKCM 19 57641013 57641013 + Missense_Mutation SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr19:57641013C>T c.970C>T c.(970-972)Ccc>Tcc p.P324S SKCM 19 57641025 57641025 + Missense_Mutation SNP C C T TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr19:57641025C>T c.982C>T c.(982-984)Ctt>Ttt p.L328F SKCM 19 57641091 57641091 + Missense_Mutation SNP T T A TCGA-EE-A29G-06A-12D-A196-08 TCGA-EE-A29G-10A-01D-A198-08 g.chr19:57641091T>A c.1048T>A c.(1048-1050)Tta>Ata p.L350I SKCM 19 57641114 57641114 + Silent SNP C C T TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr19:57641114C>T c.1071C>T c.(1069-1071)gtC>gtT p.V357V SKCM 19 57641153 57641153 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:57641153G>A c.1110G>A c.(1108-1110)caG>caA p.Q370Q SKCM 19 57641207 57641207 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:57641207G>A c.1164G>A c.(1162-1164)atG>atA p.M388I SKCM 19 57641248 57641248 + Missense_Mutation SNP G G A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr19:57641248G>A c.1205G>A c.(1204-1206)gGg>gAg p.G402E SKCM 19 57641322 57641322 + Missense_Mutation SNP A A G TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr19:57641322A>G c.1279A>G c.(1279-1281)Aat>Gat p.N427D SKCM 19 57641411 57641411 + Silent SNP C C T TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr19:57641411C>T c.1368C>T c.(1366-1368)atC>atT p.I456I SKCM 19 57641439 57641439 + Missense_Mutation SNP C C T TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr19:57641439C>T c.1396C>T c.(1396-1398)Cct>Tct p.P466S SKCM 19 57641478 57641478 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr19:57641478G>A c.1435G>A c.(1435-1437)Gaa>Aaa p.E479K SKCM 19 57641516 57641516 + Silent SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr19:57641516G>A c.1473G>A c.(1471-1473)caG>caA p.Q491Q SKCM 19 57641622 57641622 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr19:57641622G>A c.1579G>A c.(1579-1581)Gag>Aag p.E527K SKCM 19 57641670 57641670 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:57641670G>A c.1627G>A c.(1627-1629)Gaa>Aaa p.E543K SKCM 19 57641750 57641750 + Missense_Mutation SNP G G A TCGA-GN-A4U8-06A-11D-A32N-08 TCGA-GN-A4U8-10B-01D-A32N-08 g.chr19:57641750G>A c.1707G>A c.(1705-1707)atG>atA p.M569I SKCM 19 57641786 57641786 + Missense_Mutation SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr19:57641786G>A c.1743G>A c.(1741-1743)atG>atA p.M581I SKCM 19 57641808 57641808 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr19:57641808G>A c.1765G>A c.(1765-1767)Gat>Aat p.D589N SKCM 19 57641952 57641952 + Missense_Mutation SNP G G A TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr19:57641952G>A c.1909G>A c.(1909-1911)Gat>Aat p.D637N SKCM 19 57642007 57642007 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:57642007G>A c.1964G>A c.(1963-1965)gGa>gAa p.G655E SKCM 19 57642045 57642045 + Missense_Mutation SNP A A G TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr19:57642045A>G c.2002A>G c.(2002-2004)Aag>Gag p.K668E SKCM 19 57642176 57642176 + Silent SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr19:57642176C>T c.2133C>T c.(2131-2133)tcC>tcT p.S711S SKCM 19 57642220 57642220 + Missense_Mutation SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr19:57642220G>A c.2177G>A c.(2176-2178)gGa>gAa p.G726E SKCM 19 57642237 57642237 + Nonsense_Mutation SNP G G T TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr19:57642237G>T c.2194G>T c.(2194-2196)Gaa>Taa p.E732* SKCM 19 57642372 57642372 + Nonsense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr19:57642372C>T c.2329C>T c.(2329-2331)Caa>Taa p.Q777* SKCM 19 57642421 57642421 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:57642421G>A c.2378G>A c.(2377-2379)gGa>gAa p.G793E SKCM 19 57642485 57642485 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:57642485G>A c.2442G>A c.(2440-2442)gtG>gtA p.V814V SKCM 19 57642498 57642498 + Missense_Mutation SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr19:57642498C>T c.2455C>T c.(2455-2457)Cct>Tct p.P819S SKCM 19 57642539 57642539 + Silent SNP C C T TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr19:57642539C>T c.2496C>T c.(2494-2496)atC>atT p.I832I SKCM 19 57642599 57642599 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:57642599C>T c.2556C>T c.(2554-2556)gcC>gcT p.A852A SKCM 19 57642603 57642603 + Missense_Mutation SNP T T C TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr19:57642603T>C c.2560T>C c.(2560-2562)Ttc>Ctc p.F854L SKCM 19 57642615 57642615 + Missense_Mutation SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr19:57642615G>A c.2572G>A c.(2572-2574)Gat>Aat p.D858N SKCM 19 57642615 57642615 + Missense_Mutation SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr19:57642615G>A c.2572G>A c.(2572-2574)Gat>Aat p.D858N SKCM 19 57642615 57642615 + Missense_Mutation SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr19:57642615G>A c.2572G>A c.(2572-2574)Gat>Aat p.D858N SKCM 19 57642615 57642615 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr19:57642615G>A c.2572G>A c.(2572-2574)Gat>Aat p.D858N SKCM 19 57642699 57642699 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr19:57642699G>A c.2656G>A c.(2656-2658)Ggg>Agg p.G886R SKCM 19 57642767 57642767 + Silent SNP C C T TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr19:57642767C>T c.2724C>T c.(2722-2724)atC>atT p.I908I SKCM 19 57642767 57642767 + Silent SNP C C T TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr19:57642767C>T c.2724C>T c.(2722-2724)atC>atT p.I908I SKCM 19 57642775 57642775 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr19:57642775G>A c.2732G>A c.(2731-2733)gGg>gAg p.G911E SKCM 19 57642776 57642776 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr19:57642776G>A c.2733G>A c.(2731-2733)ggG>ggA p.G911G

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 19 57647405 57647405 single base substitution G A downstream_gene_variant BLCA-US 19 57640824 57640824 single base substitution G C downstream_gene_variant BLCA-US 19 57640824 57640824 single base substitution G C missense_variant E261Q 781G>C BLCA-US 19 57640872 57640872 single base substitution G A downstream_gene_variant BLCA-US 19 57640872 57640872 single base substitution G A missense_variant D277N 829G>A BLCA-US 19 57641088 57641088 single base substitution G A downstream_gene_variant BLCA-US 19 57641088 57641088 single base substitution G A missense_variant E349K 1045G>A BLCA-US 19 57641253 57641253 single base substitution G A downstream_gene_variant BLCA-US 19 57641253 57641253 single base substitution G A missense_variant E404K 1210G>A BLCA-US 19 57642078 57642078 single base substitution G A downstream_gene_variant BLCA-US 19 57642078 57642078 single base substitution G A missense_variant E679K 2035G>A BLCA-US 19 57642777 57642777 single base substitution G A downstream_gene_variant BLCA-US 19 57642777 57642777 single base substitution G A missense_variant E912K 2734G>A BLCA-US 19 57646567 57646567 single base substitution G A downstream_gene_variant BLCA-US 19 57647056 57647056 single base substitution G C downstream_gene_variant BOCA-FR 19 57645941 57645941 single base substitution C T downstream_gene_variant BRCA-EU 19 57627523 57627523 single base substitution G A upstream_gene_variant BRCA-EU 19 57628690 57628690 single base substitution C T upstream_gene_variant BRCA-EU 19 57629352 57629352 single base substitution G A upstream_gene_variant BRCA-EU 19 57629706 57629706 single base substitution G T upstream_gene_variant BRCA-EU 19 57630247 57630247 single base substitution A G upstream_gene_variant BRCA-EU 19 57630391 57630391 single base substitution A C upstream_gene_variant BRCA-EU 19 57630822 57630822 single base substitution G A intron_variant BRCA-EU 19 57630822 57630822 single base substitution G A upstream_gene_variant BRCA-EU 19 57631232 57631232 single base substitution C T intron_variant BRCA-EU 19 57631232 57631232 single base substitution C T upstream_gene_variant BRCA-EU 19 57631486 57631486 single base substitution C T 5_prime_UTR_variant BRCA-EU 19 57631486 57631486 single base substitution C T intron_variant BRCA-EU 19 57631723 57631723 single base substitution C T intron_variant BRCA-EU 19 57631756 57631756 single base substitution T A intron_variant BRCA-EU 19 57631776 57631776 single base substitution T C intron_variant BRCA-EU 19 57632248 57632248 single base substitution G A intron_variant BRCA-EU 19 57633102 57633103 deletion of <=200bp TA - intron_variant BRCA-EU 19 57633452 57633452 single base substitution C T intron_variant BRCA-EU 19 57633716 57633716 single base substitution A G 5_prime_UTR_variant BRCA-EU 19 57635487 57635487 single base substitution C T 5_prime_UTR_variant BRCA-EU 19 57635487 57635487 single base substitution C T upstream_gene_variant BRCA-EU 19 57635797 57635797 single base substitution C T intron_variant BRCA-EU 19 57635797 57635797 single base substitution C T upstream_gene_variant BRCA-EU 19 57636159 57636159 single base substitution G A intron_variant BRCA-EU 19 57636159 57636159 single base substitution G A upstream_gene_variant BRCA-EU 19 57636945 57636945 single base substitution G C intron_variant BRCA-EU 19 57636945 57636945 single base substitution G C upstream_gene_variant BRCA-EU 19 57637199 57637199 single base substitution C T intron_variant BRCA-EU 19 57637199 57637199 single base substitution C T upstream_gene_variant BRCA-EU 19 57637424 57637424 single base substitution A G intron_variant BRCA-EU 19 57637424 57637424 single base substitution A G upstream_gene_variant BRCA-EU 19 57638116 57638116 single base substitution A G intron_variant BRCA-EU 19 57638116 57638116 single base substitution A G upstream_gene_variant BRCA-EU 19 57638571 57638571 single base substitution C A intron_variant BRCA-EU 19 57638571 57638571 single base substitution C A upstream_gene_variant BRCA-EU 19 57639132 57639132 single base substitution G T intron_variant BRCA-EU 19 57639132 57639132 single base substitution G T upstream_gene_variant BRCA-EU 19 57639135 57639135 single base substitution C G intron_variant BRCA-EU 19 57639135 57639135 single base substitution C G upstream_gene_variant BRCA-EU 19 57639432 57639432 single base substitution C A intron_variant BRCA-EU 19 57639432 57639432 single base substitution C A upstream_gene_variant BRCA-EU 19 57639915 57639915 single base substitution T C intron_variant BRCA-EU 19 57639915 57639915 single base substitution T C upstream_gene_variant BRCA-EU 19 57641119 57641119 single base substitution C T downstream_gene_variant BRCA-EU 19 57641119 57641119 single base substitution C T missense_variant S359L 1076C>T BRCA-EU 19 57641371 57641371 single base substitution A C downstream_gene_variant BRCA-EU 19 57641371 57641371 single base substitution A C missense_variant H443P 1328A>C BRCA-EU 19 57642962 57642962 single base substitution T G 3_prime_UTR_variant BRCA-EU 19 57642962 57642962 single base substitution T G downstream_gene_variant BRCA-EU 19 57643598 57643598 single base substitution A C downstream_gene_variant BRCA-EU 19 57643682 57643682 single base substitution C T downstream_gene_variant BRCA-EU 19 57644872 57644872 single base substitution A C downstream_gene_variant BRCA-EU 19 57644896 57644896 single base substitution G C downstream_gene_variant BRCA-EU 19 57645512 57645512 insertion of <=200bp - A downstream_gene_variant BRCA-EU 19 57645665 57645665 single base substitution G C downstream_gene_variant BRCA-EU 19 57646318 57646318 single base substitution C G downstream_gene_variant BRCA-EU 19 57646387 57646387 insertion of <=200bp - T downstream_gene_variant BRCA-EU 19 57646501 57646501 single base substitution G A downstream_gene_variant BRCA-EU 19 57646670 57646670 single base substitution G A downstream_gene_variant BRCA-EU 19 57646882 57646882 single base substitution C T downstream_gene_variant BRCA-EU 19 57646951 57646951 single base substitution G A downstream_gene_variant BRCA-EU 19 57647158 57647158 single base substitution G C downstream_gene_variant BRCA-EU 19 57647930 57647930 single base substitution G A downstream_gene_variant BRCA-EU 19 57647966 57647966 single base substitution A T downstream_gene_variant BRCA-FR 19 57633452 57633452 single base substitution C T intron_variant BRCA-FR 19 57635487 57635487 single base substitution C T 5_prime_UTR_variant BRCA-FR 19 57635487 57635487 single base substitution C T upstream_gene_variant BRCA-FR 19 57638571 57638571 single base substitution C A intron_variant BRCA-FR 19 57638571 57638571 single base substitution C A upstream_gene_variant BRCA-FR 19 57646670 57646670 single base substitution G A downstream_gene_variant BRCA-US 19 57640254 57640254 single base substitution C T downstream_gene_variant BRCA-US 19 57640254 57640254 single base substitution C T missense_variant H71Y 211C>T BRCA-US 19 57640371 57640371 single base substitution C T downstream_gene_variant BRCA-US 19 57640371 57640371 single base substitution C T missense_variant P110S 328C>T BRCA-US 19 57640903 57640903 single base substitution T C downstream_gene_variant BRCA-US 19 57640903 57640903 single base substitution T C missense_variant F287S 860T>C BRCA-US 19 57641241 57641241 single base substitution G T downstream_gene_variant BRCA-US 19 57641241 57641241 single base substitution G T stop_gained E400* 1198G>T BRCA-US 19 57641328 57641328 single base substitution G C downstream_gene_variant BRCA-US 19 57641328 57641328 single base substitution G C missense_variant E429Q 1285G>C BRCA-US 19 57642432 57642432 single base substitution A C downstream_gene_variant BRCA-US 19 57642432 57642432 single base substitution A C missense_variant I797L 2389A>C BRCA-US 19 57646297 57646297 single base substitution G A downstream_gene_variant BRCA-US 19 57646979 57646979 single base substitution C G downstream_gene_variant BRCA-US 19 57647189 57647189 single base substitution A G downstream_gene_variant BRCA-US 19 57647274 57647274 single base substitution T A downstream_gene_variant BRCA-US 19 57647337 57647337 single base substitution G C downstream_gene_variant BTCA-JP 19 57641466 57641466 single base substitution C A downstream_gene_variant BTCA-JP 19 57641466 57641466 single base substitution C A missense_variant L475I 1423C>A BTCA-JP 19 57642077 57642077 single base substitution C T downstream_gene_variant BTCA-JP 19 57642077 57642077 single base substitution C T synonymous_variant V678V 2034C>T BTCA-JP 19 57642102 57642102 single base substitution C A downstream_gene_variant BTCA-JP 19 57642102 57642102 single base substitution C A missense_variant Q687K 2059C>A BTCA-JP 19 57642378 57642378 single base substitution G A downstream_gene_variant BTCA-JP 19 57642378 57642378 single base substitution G A missense_variant A779T 2335G>A BTCA-JP 19 57642493 57642493 single base substitution G C downstream_gene_variant BTCA-JP 19 57642493 57642493 single base substitution G C missense_variant G817A 2450G>C BTCA-JP 19 57642519 57642519 single base substitution A G downstream_gene_variant BTCA-JP 19 57642519 57642519 single base substitution A G missense_variant I826V 2476A>G BTCA-JP 19 57642683 57642683 single base substitution C A downstream_gene_variant BTCA-JP 19 57642683 57642683 single base substitution C A missense_variant F880L 2640C>A BTCA-JP 19 57647478 57647478 deletion of <=200bp A - downstream_gene_variant CESC-US 19 57640514 57640514 single base substitution G C downstream_gene_variant CESC-US 19 57640514 57640514 single base substitution G C synonymous_variant V157V 471G>C CESC-US 19 57641166 57641166 single base substitution G T downstream_gene_variant CESC-US 19 57641166 57641166 single base substitution G T stop_gained E375* 1123G>T CESC-US 19 57641463 57641463 single base substitution G C downstream_gene_variant CESC-US 19 57641463 57641463 single base substitution G C missense_variant D474H 1420G>C CESC-US 19 57641624 57641624 single base substitution G T downstream_gene_variant CESC-US 19 57641624 57641624 single base substitution G T missense_variant E527D 1581G>T CESC-US 19 57641688 57641688 single base substitution C T downstream_gene_variant CESC-US 19 57641688 57641688 single base substitution C T missense_variant L549F 1645C>T CLLE-ES 19 57629734 57629734 single base substitution C T upstream_gene_variant CLLE-ES 19 57637266 57637266 single base substitution T G intron_variant CLLE-ES 19 57637266 57637266 single base substitution T G upstream_gene_variant CLLE-ES 19 57643740 57643740 single base substitution G C downstream_gene_variant COAD-US 19 57640238 57640238 insertion of <=200bp - A downstream_gene_variant COAD-US 19 57640238 57640238 insertion of <=200bp - A frameshift_variant C65*? COAD-US 19 57640239 57640239 deletion of <=200bp A - downstream_gene_variant COAD-US 19 57640239 57640239 deletion of <=200bp A - frameshift_variant K66 COAD-US 19 57640520 57640520 single base substitution G A downstream_gene_variant COAD-US 19 57640520 57640520 single base substitution G A synonymous_variant K159K 477G>A COAD-US 19 57640585 57640585 single base substitution A G downstream_gene_variant COAD-US 19 57640585 57640585 single base substitution A G missense_variant E181G 542A>G COAD-US 19 57640827 57640827 single base substitution C T downstream_gene_variant COAD-US 19 57640827 57640827 single base substitution C T missense_variant H262Y 784C>T COAD-US 19 57640930 57640930 single base substitution T G downstream_gene_variant COAD-US 19 57640930 57640930 single base substitution T G missense_variant M296R 887T>G COAD-US 19 57641106 57641106 deletion of <=200bp A - downstream_gene_variant COAD-US 19 57641106 57641106 deletion of <=200bp A - frameshift_variant K355 COAD-US 19 57641631 57641631 single base substitution T G downstream_gene_variant COAD-US 19 57641631 57641631 single base substitution T G missense_variant Y530D 1588T>G COAD-US 19 57641884 57641884 single base substitution G T downstream_gene_variant COAD-US 19 57641884 57641884 single base substitution G T missense_variant S614I 1841G>T COAD-US 19 57642089 57642089 single base substitution T C downstream_gene_variant COAD-US 19 57642089 57642089 single base substitution T C synonymous_variant L682L 2046T>C COAD-US 19 57642098 57642098 single base substitution G A downstream_gene_variant COAD-US 19 57642098 57642098 single base substitution G A synonymous_variant V685V 2055G>A COAD-US 19 57646570 57646570 single base substitution T C downstream_gene_variant COAD-US 19 57647015 57647015 single base substitution A G downstream_gene_variant COAD-US 19 57647236 57647236 single base substitution T C downstream_gene_variant COAD-US 19 57648277 57648277 single base substitution A T downstream_gene_variant COCA-CN 19 57640667 57640667 single base substitution G T downstream_gene_variant COCA-CN 19 57640667 57640667 single base substitution G T missense_variant K208N 624G>T COCA-CN 19 57641066 57641066 single base substitution C A downstream_gene_variant COCA-CN 19 57641066 57641066 single base substitution C A missense_variant F341L 1023C>A COCA-CN 19 57641088 57641088 single base substitution G T downstream_gene_variant COCA-CN 19 57641088 57641088 single base substitution G T stop_gained E349* 1045G>T COCA-CN 19 57641091 57641091 single base substitution T G downstream_gene_variant COCA-CN 19 57641091 57641091 single base substitution T G missense_variant L350V 1048T>G COCA-CN 19 57641161 57641161 single base substitution C T downstream_gene_variant COCA-CN 19 57641161 57641161 single base substitution C T missense_variant A373V 1118C>T COCA-CN 19 57646302 57646302 single base substitution C T downstream_gene_variant COCA-CN 19 57646469 57646469 single base substitution A G downstream_gene_variant COCA-CN 19 57646632 57646632 single base substitution G A downstream_gene_variant COCA-CN 19 57646699 57646699 single base substitution T C downstream_gene_variant COCA-CN 19 57646964 57646964 single base substitution T G downstream_gene_variant COCA-CN 19 57647034 57647034 single base substitution T G downstream_gene_variant EOPC-DE 19 57628124 57628124 single base substitution G A upstream_gene_variant ESAD-UK 19 57625745 57625745 single base substitution T C upstream_gene_variant ESAD-UK 19 57626989 57626989 single base substitution T C upstream_gene_variant ESAD-UK 19 57627033 57627033 single base substitution T G upstream_gene_variant ESAD-UK 19 57627324 57627324 single base substitution A G upstream_gene_variant ESAD-UK 19 57628123 57628123 single base substitution C T upstream_gene_variant ESAD-UK 19 57628491 57628491 single base substitution C A upstream_gene_variant ESAD-UK 19 57628540 57628540 single base substitution T G upstream_gene_variant ESAD-UK 19 57628660 57628660 single base substitution G T upstream_gene_variant ESAD-UK 19 57628927 57628927 single base substitution G C upstream_gene_variant ESAD-UK 19 57629320 57629320 single base substitution A G upstream_gene_variant ESAD-UK 19 57629375 57629375 single base substitution C A upstream_gene_variant ESAD-UK 19 57629407 57629407 single base substitution A C upstream_gene_variant ESAD-UK 19 57629508 57629508 single base substitution A G upstream_gene_variant ESAD-UK 19 57630534 57630534 single base substitution C T 5_prime_UTR_variant ESAD-UK 19 57630534 57630534 single base substitution C T upstream_gene_variant ESAD-UK 19 57631094 57631094 single base substitution A G intron_variant ESAD-UK 19 57631094 57631094 single base substitution A G upstream_gene_variant ESAD-UK 19 57631892 57631892 single base substitution C T intron_variant ESAD-UK 19 57631918 57631918 single base substitution G A intron_variant ESAD-UK 19 57633021 57633021 single base substitution T G intron_variant ESAD-UK 19 57633298 57633298 single base substitution C T intron_variant ESAD-UK 19 57633644 57633644 single base substitution C T intron_variant ESAD-UK 19 57634250 57634250 single base substitution A C intron_variant ESAD-UK 19 57634515 57634515 single base substitution G T intron_variant ESAD-UK 19 57634545 57634545 single base substitution C G intron_variant ESAD-UK 19 57634675 57634675 single base substitution A T intron_variant ESAD-UK 19 57635332 57635332 single base substitution A C intron_variant ESAD-UK 19 57635332 57635332 single base substitution A C upstream_gene_variant ESAD-UK 19 57635353 57635353 single base substitution G C intron_variant ESAD-UK 19 57635353 57635353 single base substitution G C upstream_gene_variant ESAD-UK 19 57635836 57635836 single base substitution T G intron_variant ESAD-UK 19 57635836 57635836 single base substitution T G upstream_gene_variant ESAD-UK 19 57636192 57636192 single base substitution T C intron_variant ESAD-UK 19 57636192 57636192 single base substitution T C upstream_gene_variant ESAD-UK 19 57636379 57636379 single base substitution C A intron_variant ESAD-UK 19 57636379 57636379 single base substitution C A upstream_gene_variant ESAD-UK 19 57637041 57637041 single base substitution G A intron_variant ESAD-UK 19 57637041 57637041 single base substitution G A upstream_gene_variant ESAD-UK 19 57637424 57637424 single base substitution A C intron_variant ESAD-UK 19 57637424 57637424 single base substitution A C upstream_gene_variant ESAD-UK 19 57637470 57637470 single base substitution T C intron_variant ESAD-UK 19 57637470 57637470 single base substitution T C upstream_gene_variant ESAD-UK 19 57637690 57637690 single base substitution A C intron_variant ESAD-UK 19 57637690 57637690 single base substitution A C upstream_gene_variant ESAD-UK 19 57637690 57637690 single base substitution A G intron_variant ESAD-UK 19 57637690 57637690 single base substitution A G upstream_gene_variant ESAD-UK 19 57638342 57638342 single base substitution G T intron_variant ESAD-UK 19 57638342 57638342 single base substitution G T upstream_gene_variant ESAD-UK 19 57638495 57638495 single base substitution C T intron_variant ESAD-UK 19 57638495 57638495 single base substitution C T upstream_gene_variant ESAD-UK 19 57639334 57639334 single base substitution G A intron_variant ESAD-UK 19 57639334 57639334 single base substitution G A upstream_gene_variant ESAD-UK 19 57639490 57639490 single base substitution T G intron_variant ESAD-UK 19 57639490 57639490 single base substitution T G upstream_gene_variant ESAD-UK 19 57639492 57639492 single base substitution A C intron_variant ESAD-UK 19 57639492 57639492 single base substitution A C upstream_gene_variant ESAD-UK 19 57639558 57639558 single base substitution A G intron_variant ESAD-UK 19 57639558 57639558 single base substitution A G upstream_gene_variant ESAD-UK 19 57639616 57639616 single base substitution A C intron_variant ESAD-UK 19 57639616 57639616 single base substitution A C upstream_gene_variant ESAD-UK 19 57639709 57639709 single base substitution A C intron_variant ESAD-UK 19 57639709 57639709 single base substitution A C upstream_gene_variant ESAD-UK 19 57640243 57640243 single base substitution A C downstream_gene_variant ESAD-UK 19 57640243 57640243 single base substitution A C missense_variant K67T 200A>C ESAD-UK 19 57640253 57640253 single base substitution T C downstream_gene_variant ESAD-UK 19 57640253 57640253 single base substitution T C synonymous_variant S70S 210T>C ESAD-UK 19 57640509 57640509 single base substitution C T downstream_gene_variant ESAD-UK 19 57640509 57640509 single base substitution C T missense_variant H156Y 466C>T ESAD-UK 19 57640585 57640585 single base substitution A T downstream_gene_variant ESAD-UK 19 57640585 57640585 single base substitution A T missense_variant E181V 542A>T ESAD-UK 19 57640749 57640749 single base substitution C T downstream_gene_variant ESAD-UK 19 57640749 57640749 single base substitution C T missense_variant P236S 706C>T ESAD-UK 19 57641061 57641061 single base substitution G T downstream_gene_variant ESAD-UK 19 57641061 57641061 single base substitution G T missense_variant D340Y 1018G>T ESAD-UK 19 57641167 57641167 single base substitution A G downstream_gene_variant ESAD-UK 19 57641167 57641167 single base substitution A G missense_variant E375G 1124A>G ESAD-UK 19 57641360 57641360 single base substitution A G downstream_gene_variant ESAD-UK 19 57641360 57641360 single base substitution A G synonymous_variant K439K 1317A>G ESAD-UK 19 57641520 57641520 single base substitution A G downstream_gene_variant ESAD-UK 19 57641520 57641520 single base substitution A G missense_variant S493G 1477A>G ESAD-UK 19 57641649 57641649 single base substitution A C downstream_gene_variant ESAD-UK 19 57641649 57641649 single base substitution A C missense_variant S536R 1606A>C ESAD-UK 19 57642224 57642224 single base substitution T A downstream_gene_variant ESAD-UK 19 57642224 57642224 single base substitution T A synonymous_variant S727S 2181T>A ESAD-UK 19 57642993 57642993 single base substitution T G 3_prime_UTR_variant ESAD-UK 19 57642993 57642993 single base substitution T G downstream_gene_variant ESAD-UK 19 57643728 57643728 single base substitution C T downstream_gene_variant ESAD-UK 19 57644630 57644630 single base substitution A G downstream_gene_variant ESAD-UK 19 57644976 57644976 single base substitution A C downstream_gene_variant ESAD-UK 19 57645989 57645989 single base substitution C A downstream_gene_variant ESAD-UK 19 57646463 57646463 single base substitution G A downstream_gene_variant ESAD-UK 19 57647637 57647637 single base substitution A G downstream_gene_variant ESAD-UK 19 57647880 57647880 single base substitution A C downstream_gene_variant ESCA-CN 19 57640666 57640666 single base substitution A T downstream_gene_variant ESCA-CN 19 57640666 57640666 single base substitution A T missense_variant K208M 623A>T ESCA-CN 19 57641241 57641241 single base substitution G A downstream_gene_variant ESCA-CN 19 57641241 57641241 single base substitution G A missense_variant E400K 1198G>A ESCA-CN 19 57641786 57641786 single base substitution G A downstream_gene_variant ESCA-CN 19 57641786 57641786 single base substitution G A missense_variant M581I 1743G>A ESCA-CN 19 57641880 57641880 single base substitution G A downstream_gene_variant ESCA-CN 19 57641880 57641880 single base substitution G A missense_variant A613T 1837G>A ESCA-CN 19 57642124 57642124 single base substitution A G downstream_gene_variant ESCA-CN 19 57642124 57642124 single base substitution A G missense_variant Y694C 2081A>G ESCA-CN 19 57642573 57642573 single base substitution G A downstream_gene_variant ESCA-CN 19 57642573 57642573 single base substitution G A missense_variant D844N 2530G>A ESCA-CN 19 57642727 57642727 single base substitution C A downstream_gene_variant ESCA-CN 19 57642727 57642727 single base substitution C A missense_variant A895E 2684C>A ESCA-CN 19 57646348 57646348 single base substitution C T downstream_gene_variant ESCA-CN 19 57646602 57646602 single base substitution C A downstream_gene_variant GBM-US 19 57641232 57641232 single base substitution A G downstream_gene_variant GBM-US 19 57641232 57641232 single base substitution A G missense_variant T397A 1189A>G GBM-US 19 57641754 57641754 single base substitution T A downstream_gene_variant GBM-US 19 57641754 57641754 single base substitution T A missense_variant S571T 1711T>A GBM-US 19 57646590 57646590 single base substitution A T downstream_gene_variant GBM-US 19 57647409 57647409 single base substitution C G downstream_gene_variant KIRC-US 19 57640818 57640818 single base substitution G T downstream_gene_variant KIRC-US 19 57640818 57640818 single base substitution G T stop_gained E259* 775G>T KIRC-US 19 57642541 57642541 single base substitution G A downstream_gene_variant KIRC-US 19 57642541 57642541 single base substitution G A missense_variant G833E 2498G>A KIRC-US 19 57642738 57642738 single base substitution C A downstream_gene_variant KIRC-US 19 57642738 57642738 single base substitution C A synonymous_variant R899R 2695C>A KIRC-US 19 57642739 57642739 single base substitution G T downstream_gene_variant KIRC-US 19 57642739 57642739 single base substitution G T missense_variant R899L 2696G>T KIRC-US 19 57642746 57642746 single base substitution T C downstream_gene_variant KIRC-US 19 57642746 57642746 single base substitution T C synonymous_variant P901P 2703T>C KIRC-US 19 57646742 57646742 single base substitution A T downstream_gene_variant KIRC-US 19 57646763 57646763 single base substitution C T downstream_gene_variant KIRP-US 19 57641187 57641187 single base substitution G C downstream_gene_variant KIRP-US 19 57641187 57641187 single base substitution G C missense_variant D382H 1144G>C LAML-KR 19 57642098 57642098 single base substitution G A downstream_gene_variant LAML-KR 19 57642098 57642098 single base substitution G A synonymous_variant V685V 2055G>A LAML-KR 19 57646570 57646570 single base substitution T C downstream_gene_variant LAML-KR 19 57648277 57648277 single base substitution A T downstream_gene_variant LIAD-FR 19 57641414 57641414 single base substitution C T downstream_gene_variant LIAD-FR 19 57641414 57641414 single base substitution C T synonymous_variant N457N 1371C>T LICA-CN 19 57640568 57640568 single base substitution T A downstream_gene_variant LICA-CN 19 57640568 57640568 single base substitution T A synonymous_variant S175S 525T>A LICA-CN 19 57640634 57640634 single base substitution A T downstream_gene_variant LICA-CN 19 57640634 57640634 single base substitution A T synonymous_variant T197T 591A>T LICA-CN 19 57641963 57641963 single base substitution C T downstream_gene_variant LICA-CN 19 57641963 57641963 single base substitution C T synonymous_variant I640I 1920C>T LICA-CN 19 57646517 57646517 single base substitution A G downstream_gene_variant LICA-FR 19 57629654 57629654 single base substitution T A upstream_gene_variant LICA-FR 19 57640248 57640248 single base substitution C A downstream_gene_variant LICA-FR 19 57640248 57640248 single base substitution C A missense_variant Q69K 205C>A LICA-FR 19 57640867 57640867 single base substitution C A downstream_gene_variant LICA-FR 19 57640867 57640867 single base substitution C A missense_variant P275H 824C>A LICA-FR 19 57641928 57641928 single base substitution G T downstream_gene_variant LICA-FR 19 57641928 57641928 single base substitution G T stop_gained E629* 1885G>T LICA-FR 19 57646310 57646310 single base substitution G A downstream_gene_variant LIHC-US 19 57640050 57640050 single base substitution T A missense_variant S3T 7T>A LIHC-US 19 57646378 57646378 single base substitution C A downstream_gene_variant LIHC-US 19 57646911 57646911 single base substitution G C downstream_gene_variant LIHC-US 19 57647323 57647323 single base substitution G A downstream_gene_variant LINC-JP 19 57626143 57626143 single base substitution C T upstream_gene_variant LINC-JP 19 57626986 57626986 single base substitution T C upstream_gene_variant LINC-JP 19 57628083 57628083 single base substitution G A upstream_gene_variant LINC-JP 19 57630696 57630696 single base substitution G T intron_variant LINC-JP 19 57630696 57630696 single base substitution G T upstream_gene_variant LINC-JP 19 57641561 57641561 single base substitution C T downstream_gene_variant LINC-JP 19 57641561 57641561 single base substitution C T synonymous_variant V506V 1518C>T LINC-JP 19 57642377 57642377 single base substitution G A downstream_gene_variant LINC-JP 19 57642377 57642377 single base substitution G A synonymous_variant K778K 2334G>A LINC-JP 19 57645171 57645171 single base substitution A T downstream_gene_variant LINC-JP 19 57647900 57647900 single base substitution C T downstream_gene_variant LIRI-JP 19 57625823 57625823 single base substitution T C upstream_gene_variant LIRI-JP 19 57626329 57626329 single base substitution T C upstream_gene_variant LIRI-JP 19 57626495 57626495 insertion of <=200bp - AGT upstream_gene_variant LIRI-JP 19 57627972 57627972 single base substitution C A upstream_gene_variant LIRI-JP 19 57627973 57627973 single base substitution C T upstream_gene_variant LIRI-JP 19 57628836 57628836 single base substitution A T upstream_gene_variant LIRI-JP 19 57628999 57628999 single base substitution G T upstream_gene_variant LIRI-JP 19 57629838 57629838 single base substitution A T upstream_gene_variant LIRI-JP 19 57629877 57629877 single base substitution C T upstream_gene_variant LIRI-JP 19 57630104 57630104 single base substitution A T upstream_gene_variant LIRI-JP 19 57630732 57630732 single base substitution A C intron_variant LIRI-JP 19 57630732 57630732 single base substitution A C upstream_gene_variant LIRI-JP 19 57634602 57634602 single base substitution A G intron_variant LIRI-JP 19 57634778 57634778 single base substitution G T intron_variant LIRI-JP 19 57635098 57635098 single base substitution C A intron_variant LIRI-JP 19 57635098 57635098 single base substitution C A upstream_gene_variant LIRI-JP 19 57635126 57635126 single base substitution C T intron_variant LIRI-JP 19 57635126 57635126 single base substitution C T upstream_gene_variant LIRI-JP 19 57635140 57635140 single base substitution A G intron_variant LIRI-JP 19 57635140 57635140 single base substitution A G upstream_gene_variant LIRI-JP 19 57636360 57636360 single base substitution A G intron_variant LIRI-JP 19 57636360 57636360 single base substitution A G upstream_gene_variant LIRI-JP 19 57636659 57636659 single base substitution A G intron_variant LIRI-JP 19 57636659 57636659 single base substitution A G upstream_gene_variant LIRI-JP 19 57637803 57637803 single base substitution T C intron_variant LIRI-JP 19 57637803 57637803 single base substitution T C upstream_gene_variant LIRI-JP 19 57637923 57637923 single base substitution T C intron_variant LIRI-JP 19 57637923 57637923 single base substitution T C upstream_gene_variant LIRI-JP 19 57638665 57638665 single base substitution G A intron_variant LIRI-JP 19 57638665 57638665 single base substitution G A upstream_gene_variant LIRI-JP 19 57639752 57639752 single base substitution T C intron_variant LIRI-JP 19 57639752 57639752 single base substitution T C upstream_gene_variant LIRI-JP 19 57639957 57639957 single base substitution A G intron_variant LIRI-JP 19 57639957 57639957 single base substitution A G upstream_gene_variant LIRI-JP 19 57640873 57640873 single base substitution A G downstream_gene_variant LIRI-JP 19 57640873 57640873 single base substitution A G missense_variant D277G 830A>G LIRI-JP 19 57640902 57640902 single base substitution T G downstream_gene_variant LIRI-JP 19 57640902 57640902 single base substitution T G missense_variant F287V 859T>G LIRI-JP 19 57641590 57641590 single base substitution T C downstream_gene_variant LIRI-JP 19 57641590 57641590 single base substitution T C missense_variant F516S 1547T>C LIRI-JP 19 57641674 57641674 single base substitution G A downstream_gene_variant LIRI-JP 19 57641674 57641674 single base substitution G A missense_variant S544N 1631G>A LIRI-JP 19 57642786 57642786 single base substitution G A downstream_gene_variant LIRI-JP 19 57642786 57642786 single base substitution G A missense_variant G915S 2743G>A LIRI-JP 19 57644564 57644564 single base substitution G T downstream_gene_variant LIRI-JP 19 57644565 57644565 single base substitution C G downstream_gene_variant LIRI-JP 19 57645300 57645300 single base substitution A G downstream_gene_variant LIRI-JP 19 57646555 57646555 insertion of <=200bp - T downstream_gene_variant LIRI-JP 19 57646575 57646575 single base substitution T C downstream_gene_variant LIRI-JP 19 57647364 57647364 single base substitution G A downstream_gene_variant LUSC-KR 19 57626743 57626743 single base substitution T C upstream_gene_variant LUSC-KR 19 57629036 57629036 single base substitution C T upstream_gene_variant LUSC-KR 19 57629238 57629238 single base substitution C A upstream_gene_variant LUSC-KR 19 57635558 57635558 single base substitution C T intron_variant LUSC-KR 19 57635558 57635558 single base substitution C T upstream_gene_variant LUSC-KR 19 57636039 57636039 single base substitution G A intron_variant LUSC-KR 19 57636039 57636039 single base substitution G A upstream_gene_variant LUSC-KR 19 57636249 57636249 single base substitution T A intron_variant LUSC-KR 19 57636249 57636249 single base substitution T A upstream_gene_variant LUSC-KR 19 57636961 57636961 single base substitution T A intron_variant LUSC-KR 19 57636961 57636961 single base substitution T A upstream_gene_variant LUSC-KR 19 57637070 57637070 single base substitution C T intron_variant LUSC-KR 19 57637070 57637070 single base substitution C T upstream_gene_variant LUSC-KR 19 57639783 57639783 single base substitution C A intron_variant LUSC-KR 19 57639783 57639783 single base substitution C A upstream_gene_variant LUSC-KR 19 57640314 57640314 single base substitution G A downstream_gene_variant LUSC-KR 19 57640314 57640314 single base substitution G A missense_variant D91N 271G>A LUSC-KR 19 57640664 57640664 single base substitution G T downstream_gene_variant LUSC-KR 19 57640664 57640664 single base substitution G T missense_variant R207S 621G>T LUSC-KR 19 57641086 57641086 single base substitution G A downstream_gene_variant LUSC-KR 19 57641086 57641086 single base substitution G A missense_variant R348K 1043G>A LUSC-KR 19 57641799 57641799 single base substitution G A downstream_gene_variant LUSC-KR 19 57641799 57641799 single base substitution G A missense_variant E586K 1756G>A LUSC-KR 19 57642036 57642036 single base substitution G T downstream_gene_variant LUSC-KR 19 57642036 57642036 single base substitution G T missense_variant D665Y 1993G>T LUSC-KR 19 57642052 57642052 single base substitution T A downstream_gene_variant LUSC-KR 19 57642052 57642052 single base substitution T A missense_variant I670N 2009T>A LUSC-KR 19 57642483 57642483 single base substitution G T downstream_gene_variant LUSC-KR 19 57642483 57642483 single base substitution G T missense_variant V814L 2440G>T LUSC-KR 19 57646218 57646218 single base substitution C T downstream_gene_variant LUSC-KR 19 57646249 57646249 single base substitution C T downstream_gene_variant LUSC-KR 19 57646302 57646302 single base substitution C A downstream_gene_variant LUSC-US 19 57640074 57640074 single base substitution C T stop_gained Q11* 31C>T LUSC-US 19 57640084 57640084 single base substitution G A downstream_gene_variant LUSC-US 19 57640084 57640084 single base substitution G A missense_variant S14N 41G>A LUSC-US 19 57640100 57640100 single base substitution G C downstream_gene_variant LUSC-US 19 57640100 57640100 single base substitution G C missense_variant M19I 57G>C LUSC-US 19 57640252 57640252 single base substitution G T downstream_gene_variant LUSC-US 19 57640252 57640252 single base substitution G T missense_variant S70I 209G>T LUSC-US 19 57640425 57640425 single base substitution G T downstream_gene_variant LUSC-US 19 57640425 57640425 single base substitution G T stop_gained E128* 382G>T LUSC-US 19 57640572 57640572 single base substitution G T downstream_gene_variant LUSC-US 19 57640572 57640572 single base substitution G T missense_variant V177L 529G>T LUSC-US 19 57640619 57640619 single base substitution C G downstream_gene_variant LUSC-US 19 57640619 57640619 single base substitution C G missense_variant N192K 576C>G LUSC-US 19 57640692 57640692 single base substitution G C downstream_gene_variant LUSC-US 19 57640692 57640692 single base substitution G C missense_variant E217Q 649G>C LUSC-US 19 57640894 57640894 single base substitution A T downstream_gene_variant LUSC-US 19 57640894 57640894 single base substitution A T missense_variant Q284L 851A>T LUSC-US 19 57640914 57640914 single base substitution G A downstream_gene_variant LUSC-US 19 57640914 57640914 single base substitution G A missense_variant G291R 871G>A LUSC-US 19 57641067 57641067 single base substitution T C downstream_gene_variant LUSC-US 19 57641067 57641067 single base substitution T C missense_variant C342R 1024T>C LUSC-US 19 57641313 57641313 single base substitution G T downstream_gene_variant LUSC-US 19 57641313 57641313 single base substitution G T missense_variant V424F 1270G>T LUSC-US 19 57641512 57641512 single base substitution A C downstream_gene_variant LUSC-US 19 57641512 57641512 single base substitution A C missense_variant K490T 1469A>C LUSC-US 19 57641900 57641900 single base substitution G C downstream_gene_variant LUSC-US 19 57641900 57641900 single base substitution G C missense_variant Q619H 1857G>C LUSC-US 19 57642468 57642468 single base substitution G T downstream_gene_variant LUSC-US 19 57642468 57642468 single base substitution G T stop_gained E809* 2425G>T LUSC-US 19 57642610 57642610 single base substitution A G downstream_gene_variant LUSC-US 19 57642610 57642610 single base substitution A G missense_variant Y856C 2567A>G LUSC-US 19 57642683 57642683 single base substitution C T downstream_gene_variant LUSC-US 19 57642683 57642683 single base substitution C T synonymous_variant F880F 2640C>T LUSC-US 19 57642748 57642748 single base substitution G C downstream_gene_variant LUSC-US 19 57642748 57642748 single base substitution G C missense_variant S902T 2705G>C LUSC-US 19 57642755 57642755 single base substitution G T downstream_gene_variant LUSC-US 19 57642755 57642755 single base substitution G T missense_variant Q904H 2712G>T LUSC-US 19 57646494 57646494 single base substitution G C downstream_gene_variant LUSC-US 19 57646678 57646678 single base substitution C A downstream_gene_variant LUSC-US 19 57646928 57646928 single base substitution G T downstream_gene_variant LUSC-US 19 57646983 57646983 single base substitution T G downstream_gene_variant LUSC-US 19 57647047 57647047 single base substitution C G downstream_gene_variant MALY-DE 19 57630224 57630224 single base substitution A G upstream_gene_variant MALY-DE 19 57635522 57635522 single base substitution G A intron_variant MALY-DE 19 57635522 57635522 single base substitution G A upstream_gene_variant MALY-DE 19 57636411 57636411 single base substitution T C intron_variant MALY-DE 19 57636411 57636411 single base substitution T C upstream_gene_variant MALY-DE 19 57638899 57638899 single base substitution C T intron_variant MALY-DE 19 57638899 57638899 single base substitution C T upstream_gene_variant MALY-DE 19 57641164 57641164 single base substitution A G downstream_gene_variant MALY-DE 19 57641164 57641164 single base substitution A G missense_variant H374R 1121A>G MALY-DE 19 57644381 57644381 single base substitution A C downstream_gene_variant MALY-DE 19 57648040 57648040 single base substitution A G downstream_gene_variant MELA-AU 19 57625522 57625522 single base substitution G A upstream_gene_variant MELA-AU 19 57625554 57625554 single base substitution A G upstream_gene_variant MELA-AU 19 57625563 57625563 single base substitution C T upstream_gene_variant MELA-AU 19 57625629 57625629 single base substitution C T upstream_gene_variant MELA-AU 19 57625732 57625732 single base substitution C T upstream_gene_variant MELA-AU 19 57625755 57625755 single base substitution G A upstream_gene_variant MELA-AU 19 57625765 57625765 single base substitution A T upstream_gene_variant MELA-AU 19 57626176 57626176 single base substitution G A upstream_gene_variant MELA-AU 19 57626207 57626207 single base substitution G A upstream_gene_variant MELA-AU 19 57626212 57626212 single base substitution A G upstream_gene_variant MELA-AU 19 57626254 57626254 single base substitution C T upstream_gene_variant MELA-AU 19 57626428 57626428 single base substitution C T upstream_gene_variant MELA-AU 19 57626561 57626561 single base substitution C T upstream_gene_variant MELA-AU 19 57626752 57626752 single base substitution G A upstream_gene_variant MELA-AU 19 57626769 57626769 single base substitution C T upstream_gene_variant MELA-AU 19 57626829 57626829 single base substitution C T upstream_gene_variant MELA-AU 19 57626899 57626899 single base substitution C T upstream_gene_variant MELA-AU 19 57626996 57626996 single base substitution C T upstream_gene_variant MELA-AU 19 57627035 57627035 single base substitution C T upstream_gene_variant MELA-AU 19 57627038 57627038 single base substitution C T upstream_gene_variant MELA-AU 19 57627039 57627039 single base substitution C T upstream_gene_variant MELA-AU 19 57627045 57627045 single base substitution C T upstream_gene_variant MELA-AU 19 57627094 57627094 single base substitution C T upstream_gene_variant MELA-AU 19 57627095 57627095 single base substitution C T upstream_gene_variant MELA-AU 19 57627183 57627183 single base substitution C T upstream_gene_variant MELA-AU 19 57627190 57627190 single base substitution G A upstream_gene_variant MELA-AU 19 57627194 57627194 single base substitution C T upstream_gene_variant MELA-AU 19 57627246 57627246 single base substitution C T upstream_gene_variant MELA-AU 19 57627323 57627323 single base substitution G A upstream_gene_variant MELA-AU 19 57627365 57627365 single base substitution G A upstream_gene_variant MELA-AU 19 57627461 57627461 single base substitution G A upstream_gene_variant MELA-AU 19 57627746 57627746 single base substitution T G upstream_gene_variant MELA-AU 19 57627760 57627760 single base substitution C T upstream_gene_variant MELA-AU 19 57627906 57627906 single base substitution G A upstream_gene_variant MELA-AU 19 57627945 57627945 single base substitution G A upstream_gene_variant MELA-AU 19 57628320 57628320 single base substitution T A upstream_gene_variant MELA-AU 19 57628322 57628322 single base substitution C T upstream_gene_variant MELA-AU 19 57628415 57628415 single base substitution G A upstream_gene_variant MELA-AU 19 57628459 57628459 single base substitution T A upstream_gene_variant MELA-AU 19 57628483 57628483 single base substitution C T upstream_gene_variant MELA-AU 19 57628521 57628521 single base substitution T C upstream_gene_variant MELA-AU 19 57628532 57628532 single base substitution G A upstream_gene_variant MELA-AU 19 57628621 57628621 single base substitution G A upstream_gene_variant MELA-AU 19 57628734 57628734 single base substitution G A upstream_gene_variant MELA-AU 19 57628837 57628837 single base substitution G A upstream_gene_variant MELA-AU 19 57628850 57628850 single base substitution G A upstream_gene_variant MELA-AU 19 57628863 57628863 single base substitution A G upstream_gene_variant MELA-AU 19 57629005 57629005 single base substitution C T upstream_gene_variant MELA-AU 19 57629080 57629080 single base substitution C T upstream_gene_variant MELA-AU 19 57629112 57629112 single base substitution T C upstream_gene_variant MELA-AU 19 57629205 57629205 single base substitution C T upstream_gene_variant MELA-AU 19 57629420 57629420 single base substitution C T upstream_gene_variant MELA-AU 19 57629452 57629452 single base substitution G A upstream_gene_variant MELA-AU 19 57629457 57629457 single base substitution C T upstream_gene_variant MELA-AU 19 57629745 57629746 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 57629746 57629746 single base substitution C T upstream_gene_variant MELA-AU 19 57629799 57629800 multiple base substitution (>=2bp and <=200bp) AG CA upstream_gene_variant MELA-AU 19 57629801 57629801 single base substitution G A upstream_gene_variant MELA-AU 19 57629815 57629815 single base substitution C T upstream_gene_variant MELA-AU 19 57629845 57629845 single base substitution G A upstream_gene_variant MELA-AU 19 57629854 57629854 single base substitution G A upstream_gene_variant MELA-AU 19 57629890 57629890 single base substitution G A upstream_gene_variant MELA-AU 19 57629950 57629950 single base substitution C T upstream_gene_variant MELA-AU 19 57630115 57630116 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 57630138 57630138 single base substitution G A upstream_gene_variant MELA-AU 19 57630180 57630180 single base substitution C T upstream_gene_variant MELA-AU 19 57630446 57630446 single base substitution C T upstream_gene_variant MELA-AU 19 57630505 57630505 single base substitution C T upstream_gene_variant MELA-AU 19 57630546 57630546 single base substitution G A 5_prime_UTR_variant MELA-AU 19 57630546 57630546 single base substitution G A upstream_gene_variant MELA-AU 19 57630623 57630623 single base substitution G A intron_variant MELA-AU 19 57630623 57630623 single base substitution G A upstream_gene_variant MELA-AU 19 57630678 57630678 single base substitution C T intron_variant MELA-AU 19 57630678 57630678 single base substitution C T upstream_gene_variant MELA-AU 19 57630981 57630981 single base substitution G A intron_variant MELA-AU 19 57630981 57630981 single base substitution G A upstream_gene_variant MELA-AU 19 57631174 57631174 single base substitution G A intron_variant MELA-AU 19 57631174 57631174 single base substitution G A upstream_gene_variant MELA-AU 19 57631196 57631196 single base substitution G A intron_variant MELA-AU 19 57631196 57631196 single base substitution G A upstream_gene_variant MELA-AU 19 57631304 57631304 single base substitution C T intron_variant MELA-AU 19 57631304 57631304 single base substitution C T upstream_gene_variant MELA-AU 19 57631537 57631537 single base substitution G A 5_prime_UTR_variant MELA-AU 19 57631537 57631537 single base substitution G A intron_variant MELA-AU 19 57631552 57631552 single base substitution G A 5_prime_UTR_variant MELA-AU 19 57631552 57631552 single base substitution G A intron_variant MELA-AU 19 57631655 57631655 single base substitution C T 5_prime_UTR_variant MELA-AU 19 57631655 57631655 single base substitution C T intron_variant MELA-AU 19 57631746 57631746 single base substitution G A intron_variant MELA-AU 19 57631783 57631783 single base substitution C T intron_variant MELA-AU 19 57631923 57631923 single base substitution G A intron_variant MELA-AU 19 57631988 57631988 single base substitution C T intron_variant MELA-AU 19 57632003 57632003 single base substitution A C intron_variant MELA-AU 19 57632069 57632069 single base substitution C T intron_variant MELA-AU 19 57632193 57632194 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 57632221 57632221 single base substitution C T intron_variant MELA-AU 19 57632260 57632260 single base substitution C T intron_variant MELA-AU 19 57632289 57632289 single base substitution C T intron_variant MELA-AU 19 57632860 57632860 single base substitution T C intron_variant MELA-AU 19 57633129 57633129 single base substitution T C intron_variant MELA-AU 19 57633176 57633176 single base substitution C T intron_variant MELA-AU 19 57633279 57633279 single base substitution C T intron_variant MELA-AU 19 57633319 57633319 single base substitution A T intron_variant MELA-AU 19 57633457 57633457 single base substitution C T intron_variant MELA-AU 19 57633475 57633475 single base substitution G A intron_variant MELA-AU 19 57633507 57633507 single base substitution G A intron_variant MELA-AU 19 57633608 57633608 single base substitution C T intron_variant MELA-AU 19 57633632 57633632 single base substitution G A intron_variant MELA-AU 19 57633686 57633686 single base substitution C T splice_region_variant MELA-AU 19 57633743 57633743 single base substitution G A 5_prime_UTR_variant MELA-AU 19 57633815 57633815 single base substitution C T 5_prime_UTR_variant MELA-AU 19 57633947 57633947 single base substitution G A intron_variant MELA-AU 19 57634001 57634001 single base substitution G A intron_variant MELA-AU 19 57634044 57634044 single base substitution G A intron_variant MELA-AU 19 57634129 57634129 single base substitution A T intron_variant MELA-AU 19 57634334 57634334 single base substitution G A intron_variant MELA-AU 19 57634344 57634344 single base substitution G A intron_variant MELA-AU 19 57634365 57634365 single base substitution A G intron_variant MELA-AU 19 57634374 57634374 single base substitution G A intron_variant MELA-AU 19 57634377 57634377 single base substitution G A intron_variant MELA-AU 19 57634389 57634389 single base substitution C T intron_variant MELA-AU 19 57634397 57634397 single base substitution G A intron_variant MELA-AU 19 57634720 57634720 single base substitution C T intron_variant MELA-AU 19 57634855 57634855 single base substitution C T intron_variant MELA-AU 19 57634864 57634864 single base substitution G A intron_variant MELA-AU 19 57634884 57634884 single base substitution T C intron_variant MELA-AU 19 57634894 57634894 single base substitution G A intron_variant MELA-AU 19 57634920 57634920 single base substitution G A intron_variant MELA-AU 19 57635143 57635143 single base substitution C T intron_variant MELA-AU 19 57635143 57635143 single base substitution C T upstream_gene_variant MELA-AU 19 57635147 57635147 single base substitution G A intron_variant MELA-AU 19 57635147 57635147 single base substitution G A upstream_gene_variant MELA-AU 19 57635296 57635296 single base substitution C T intron_variant MELA-AU 19 57635296 57635296 single base substitution C T upstream_gene_variant MELA-AU 19 57635703 57635703 single base substitution C T intron_variant MELA-AU 19 57635703 57635703 single base substitution C T upstream_gene_variant MELA-AU 19 57635752 57635752 single base substitution C T intron_variant MELA-AU 19 57635752 57635752 single base substitution C T upstream_gene_variant MELA-AU 19 57635812 57635812 single base substitution C T intron_variant MELA-AU 19 57635812 57635812 single base substitution C T upstream_gene_variant MELA-AU 19 57635886 57635886 single base substitution T A intron_variant MELA-AU 19 57635886 57635886 single base substitution T A upstream_gene_variant MELA-AU 19 57635987 57635987 single base substitution C T intron_variant MELA-AU 19 57635987 57635987 single base substitution C T upstream_gene_variant MELA-AU 19 57636076 57636076 single base substitution C T intron_variant MELA-AU 19 57636076 57636076 single base substitution C T upstream_gene_variant MELA-AU 19 57636089 57636089 single base substitution C T intron_variant MELA-AU 19 57636089 57636089 single base substitution C T upstream_gene_variant MELA-AU 19 57636135 57636135 single base substitution C T intron_variant MELA-AU 19 57636135 57636135 single base substitution C T upstream_gene_variant MELA-AU 19 57636161 57636161 single base substitution G A intron_variant MELA-AU 19 57636161 57636161 single base substitution G A upstream_gene_variant MELA-AU 19 57636184 57636184 single base substitution C T intron_variant MELA-AU 19 57636184 57636184 single base substitution C T upstream_gene_variant MELA-AU 19 57636235 57636235 single base substitution C T intron_variant MELA-AU 19 57636235 57636235 single base substitution C T upstream_gene_variant MELA-AU 19 57636330 57636330 single base substitution G A intron_variant MELA-AU 19 57636330 57636330 single base substitution G A upstream_gene_variant MELA-AU 19 57636348 57636348 single base substitution C T intron_variant MELA-AU 19 57636348 57636348 single base substitution C T upstream_gene_variant MELA-AU 19 57636404 57636404 single base substitution C A intron_variant MELA-AU 19 57636404 57636404 single base substitution C A upstream_gene_variant MELA-AU 19 57636445 57636445 single base substitution C T intron_variant MELA-AU 19 57636445 57636445 single base substitution C T upstream_gene_variant MELA-AU 19 57636547 57636547 single base substitution G A intron_variant MELA-AU 19 57636547 57636547 single base substitution G A upstream_gene_variant MELA-AU 19 57636616 57636616 single base substitution G A intron_variant MELA-AU 19 57636616 57636616 single base substitution G A upstream_gene_variant MELA-AU 19 57636623 57636623 single base substitution G A intron_variant MELA-AU 19 57636623 57636623 single base substitution G A upstream_gene_variant MELA-AU 19 57636714 57636714 single base substitution C T intron_variant MELA-AU 19 57636714 57636714 single base substitution C T upstream_gene_variant MELA-AU 19 57636743 57636743 single base substitution C T intron_variant MELA-AU 19 57636743 57636743 single base substitution C T upstream_gene_variant MELA-AU 19 57636771 57636771 single base substitution C T intron_variant MELA-AU 19 57636771 57636771 single base substitution C T upstream_gene_variant MELA-AU 19 57636785 57636785 single base substitution C T intron_variant MELA-AU 19 57636785 57636785 single base substitution C T upstream_gene_variant MELA-AU 19 57636787 57636787 single base substitution A C intron_variant MELA-AU 19 57636787 57636787 single base substitution A C upstream_gene_variant MELA-AU 19 57636935 57636935 single base substitution C T intron_variant MELA-AU 19 57636935 57636935 single base substitution C T upstream_gene_variant MELA-AU 19 57636945 57636945 single base substitution G A intron_variant MELA-AU 19 57636945 57636945 single base substitution G A upstream_gene_variant MELA-AU 19 57636954 57636954 single base substitution C T intron_variant MELA-AU 19 57636954 57636954 single base substitution C T upstream_gene_variant MELA-AU 19 57637157 57637157 single base substitution G A intron_variant MELA-AU 19 57637157 57637157 single base substitution G A upstream_gene_variant MELA-AU 19 57637329 57637329 single base substitution G A intron_variant MELA-AU 19 57637329 57637329 single base substitution G A upstream_gene_variant MELA-AU 19 57637339 57637339 single base substitution C T intron_variant MELA-AU 19 57637339 57637339 single base substitution C T upstream_gene_variant MELA-AU 19 57637405 57637405 single base substitution G A intron_variant MELA-AU 19 57637405 57637405 single base substitution G A upstream_gene_variant MELA-AU 19 57637430 57637430 single base substitution C T intron_variant MELA-AU 19 57637430 57637430 single base substitution C T upstream_gene_variant MELA-AU 19 57637564 57637564 single base substitution C T intron_variant MELA-AU 19 57637564 57637564 single base substitution C T upstream_gene_variant MELA-AU 19 57637575 57637575 single base substitution A G intron_variant MELA-AU 19 57637575 57637575 single base substitution A G upstream_gene_variant MELA-AU 19 57637681 57637681 single base substitution G A intron_variant MELA-AU 19 57637681 57637681 single base substitution G A upstream_gene_variant MELA-AU 19 57637796 57637796 single base substitution C T intron_variant MELA-AU 19 57637796 57637796 single base substitution C T upstream_gene_variant MELA-AU 19 57637967 57637967 single base substitution C T intron_variant MELA-AU 19 57637967 57637967 single base substitution C T upstream_gene_variant MELA-AU 19 57637973 57637973 single base substitution C T intron_variant MELA-AU 19 57637973 57637973 single base substitution C T upstream_gene_variant MELA-AU 19 57638185 57638185 single base substitution G A intron_variant MELA-AU 19 57638185 57638185 single base substitution G A upstream_gene_variant MELA-AU 19 57638188 57638188 single base substitution C T intron_variant MELA-AU 19 57638188 57638188 single base substitution C T upstream_gene_variant MELA-AU 19 57638207 57638207 single base substitution C T intron_variant MELA-AU 19 57638207 57638207 single base substitution C T upstream_gene_variant MELA-AU 19 57638217 57638217 single base substitution G A intron_variant MELA-AU 19 57638217 57638217 single base substitution G A upstream_gene_variant MELA-AU 19 57638246 57638246 single base substitution C T intron_variant MELA-AU 19 57638246 57638246 single base substitution C T upstream_gene_variant MELA-AU 19 57638274 57638274 single base substitution G A intron_variant MELA-AU 19 57638274 57638274 single base substitution G A upstream_gene_variant MELA-AU 19 57638301 57638301 single base substitution G A intron_variant MELA-AU 19 57638301 57638301 single base substitution G A upstream_gene_variant MELA-AU 19 57638491 57638491 single base substitution C T intron_variant MELA-AU 19 57638491 57638491 single base substitution C T upstream_gene_variant MELA-AU 19 57638495 57638495 single base substitution C T intron_variant MELA-AU 19 57638495 57638495 single base substitution C T upstream_gene_variant MELA-AU 19 57638501 57638501 single base substitution G A intron_variant MELA-AU 19 57638501 57638501 single base substitution G A upstream_gene_variant MELA-AU 19 57638588 57638588 single base substitution C T intron_variant MELA-AU 19 57638588 57638588 single base substitution C T upstream_gene_variant MELA-AU 19 57638589 57638589 single base substitution C T intron_variant MELA-AU 19 57638589 57638589 single base substitution C T upstream_gene_variant MELA-AU 19 57638639 57638639 single base substitution C T intron_variant MELA-AU 19 57638639 57638639 single base substitution C T upstream_gene_variant MELA-AU 19 57638685 57638685 single base substitution G A intron_variant MELA-AU 19 57638685 57638685 single base substitution G A upstream_gene_variant MELA-AU 19 57638718 57638718 single base substitution A T intron_variant MELA-AU 19 57638718 57638718 single base substitution A T upstream_gene_variant MELA-AU 19 57638778 57638778 single base substitution C T intron_variant MELA-AU 19 57638778 57638778 single base substitution C T upstream_gene_variant MELA-AU 19 57638782 57638782 single base substitution G A intron_variant MELA-AU 19 57638782 57638782 single base substitution G A upstream_gene_variant MELA-AU 19 57638789 57638789 single base substitution G A intron_variant MELA-AU 19 57638789 57638789 single base substitution G A upstream_gene_variant MELA-AU 19 57638859 57638859 single base substitution G A intron_variant MELA-AU 19 57638859 57638859 single base substitution G A upstream_gene_variant MELA-AU 19 57638940 57638955 deletion of <=200bp AGCACTGTCCAGGGAA - intron_variant MELA-AU 19 57638940 57638955 deletion of <=200bp AGCACTGTCCAGGGAA - upstream_gene_variant MELA-AU 19 57638979 57638979 single base substitution C T intron_variant MELA-AU 19 57638979 57638979 single base substitution C T upstream_gene_variant MELA-AU 19 57639007 57639007 single base substitution C T intron_variant MELA-AU 19 57639007 57639007 single base substitution C T upstream_gene_variant MELA-AU 19 57639026 57639026 single base substitution C T intron_variant MELA-AU 19 57639026 57639026 single base substitution C T upstream_gene_variant MELA-AU 19 57639146 57639146 single base substitution G A intron_variant MELA-AU 19 57639146 57639146 single base substitution G A upstream_gene_variant MELA-AU 19 57639147 57639147 single base substitution G A intron_variant MELA-AU 19 57639147 57639147 single base substitution G A upstream_gene_variant MELA-AU 19 57639178 57639178 single base substitution G A intron_variant MELA-AU 19 57639178 57639178 single base substitution G A upstream_gene_variant MELA-AU 19 57639204 57639204 single base substitution C T intron_variant MELA-AU 19 57639204 57639204 single base substitution C T upstream_gene_variant MELA-AU 19 57639268 57639268 single base substitution G A intron_variant MELA-AU 19 57639268 57639268 single base substitution G A upstream_gene_variant MELA-AU 19 57639293 57639293 single base substitution G A intron_variant MELA-AU 19 57639293 57639293 single base substitution G A upstream_gene_variant MELA-AU 19 57639326 57639327 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 57639326 57639327 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 57639455 57639455 single base substitution G A intron_variant MELA-AU 19 57639455 57639455 single base substitution G A upstream_gene_variant MELA-AU 19 57639663 57639663 single base substitution A G intron_variant MELA-AU 19 57639663 57639663 single base substitution A G upstream_gene_variant MELA-AU 19 57639810 57639810 single base substitution C T intron_variant MELA-AU 19 57639810 57639810 single base substitution C T upstream_gene_variant MELA-AU 19 57639828 57639828 single base substitution C T intron_variant MELA-AU 19 57639828 57639828 single base substitution C T upstream_gene_variant MELA-AU 19 57639868 57639868 single base substitution A G intron_variant MELA-AU 19 57639868 57639868 single base substitution A G upstream_gene_variant MELA-AU 19 57639968 57639968 single base substitution C T intron_variant MELA-AU 19 57639968 57639968 single base substitution C T upstream_gene_variant MELA-AU 19 57640016 57640016 single base substitution T A 5_prime_UTR_variant MELA-AU 19 57640016 57640016 single base substitution T A intron_variant MELA-AU 19 57640091 57640091 single base substitution G A downstream_gene_variant MELA-AU 19 57640091 57640091 single base substitution G A synonymous_variant K16K 48G>A MELA-AU 19 57640145 57640145 single base substitution G A downstream_gene_variant MELA-AU 19 57640145 57640145 single base substitution G A synonymous_variant K34K 102G>A MELA-AU 19 57640189 57640189 single base substitution G A downstream_gene_variant MELA-AU 19 57640189 57640189 single base substitution G A missense_variant R49K 146G>A MELA-AU 19 57640194 57640194 single base substitution T C downstream_gene_variant MELA-AU 19 57640194 57640194 single base substitution T C missense_variant F51L 151T>C MELA-AU 19 57640197 57640197 single base substitution C T downstream_gene_variant MELA-AU 19 57640197 57640197 single base substitution C T stop_gained Q52* 154C>T MELA-AU 19 57640271 57640271 single base substitution G A downstream_gene_variant MELA-AU 19 57640271 57640271 single base substitution G A synonymous_variant L76L 228G>A MELA-AU 19 57640306 57640306 single base substitution C T downstream_gene_variant MELA-AU 19 57640306 57640306 single base substitution C T missense_variant S88F 263C>T MELA-AU 19 57640376 57640376 single base substitution G A downstream_gene_variant MELA-AU 19 57640376 57640376 single base substitution G A missense_variant M111I 333G>A MELA-AU 19 57640389 57640389 single base substitution G A downstream_gene_variant MELA-AU 19 57640389 57640389 single base substitution G A missense_variant D116N 346G>A MELA-AU 19 57640470 57640470 single base substitution T C downstream_gene_variant MELA-AU 19 57640470 57640470 single base substitution T C missense_variant Y143H 427T>C MELA-AU 19 57640539 57640539 single base substitution G A downstream_gene_variant MELA-AU 19 57640539 57640539 single base substitution G A missense_variant G166S 496G>A MELA-AU 19 57640770 57640770 single base substitution C T downstream_gene_variant MELA-AU 19 57640770 57640770 single base substitution C T missense_variant L243F 727C>T MELA-AU 19 57640817 57640817 single base substitution G A downstream_gene_variant MELA-AU 19 57640817 57640817 single base substitution G A synonymous_variant L258L 774G>A MELA-AU 19 57640915 57640915 single base substitution G A downstream_gene_variant MELA-AU 19 57640915 57640915 single base substitution G A missense_variant G291E 872G>A MELA-AU 19 57640962 57640962 single base substitution C T downstream_gene_variant MELA-AU 19 57640962 57640962 single base substitution C T missense_variant P307S 919C>T MELA-AU 19 57641002 57641002 single base substitution G A downstream_gene_variant MELA-AU 19 57641002 57641002 single base substitution G A stop_gained W320* 959G>A MELA-AU 19 57641015 57641015 single base substitution C T downstream_gene_variant MELA-AU 19 57641015 57641015 single base substitution C T synonymous_variant P324P 972C>T MELA-AU 19 57641114 57641114 single base substitution C T downstream_gene_variant MELA-AU 19 57641114 57641114 single base substitution C T synonymous_variant V357V 1071C>T MELA-AU 19 57641439 57641439 single base substitution C T downstream_gene_variant MELA-AU 19 57641439 57641439 single base substitution C T missense_variant P466S 1396C>T MELA-AU 19 57641504 57641504 single base substitution G A downstream_gene_variant MELA-AU 19 57641504 57641504 single base substitution G A synonymous_variant Q487Q 1461G>A MELA-AU 19 57641685 57641685 single base substitution C T downstream_gene_variant MELA-AU 19 57641685 57641685 single base substitution C T missense_variant P548S 1642C>T MELA-AU 19 57641755 57641755 single base substitution C T downstream_gene_variant MELA-AU 19 57641755 57641755 single base substitution C T missense_variant S571F 1712C>T MELA-AU 19 57641757 57641757 single base substitution G A downstream_gene_variant MELA-AU 19 57641757 57641757 single base substitution G A missense_variant E572K 1714G>A MELA-AU 19 57641770 57641770 single base substitution C T downstream_gene_variant MELA-AU 19 57641770 57641770 single base substitution C T missense_variant P576L 1727C>T MELA-AU 19 57641803 57641803 single base substitution C T downstream_gene_variant MELA-AU 19 57641803 57641803 single base substitution C T missense_variant S587F 1760C>T MELA-AU 19 57641866 57641866 single base substitution G A downstream_gene_variant MELA-AU 19 57641866 57641866 single base substitution G A missense_variant R608K 1823G>A MELA-AU 19 57641950 57641950 single base substitution G A downstream_gene_variant MELA-AU 19 57641950 57641950 single base substitution G A missense_variant R636K 1907G>A MELA-AU 19 57642007 57642007 single base substitution G A downstream_gene_variant MELA-AU 19 57642007 57642007 single base substitution G A missense_variant G655E 1964G>A MELA-AU 19 57642044 57642044 single base substitution G A downstream_gene_variant MELA-AU 19 57642044 57642044 single base substitution G A synonymous_variant G667G 2001G>A MELA-AU 19 57642050 57642050 single base substitution G A downstream_gene_variant MELA-AU 19 57642050 57642050 single base substitution G A synonymous_variant L669L 2007G>A MELA-AU 19 57642117 57642117 single base substitution C T downstream_gene_variant MELA-AU 19 57642117 57642117 single base substitution C T stop_gained Q692* 2074C>T MELA-AU 19 57642208 57642208 single base substitution G A downstream_gene_variant MELA-AU 19 57642208 57642208 single base substitution G A missense_variant R722K 2165G>A MELA-AU 19 57642390 57642390 single base substitution C T downstream_gene_variant MELA-AU 19 57642390 57642390 single base substitution C T missense_variant H783Y 2347C>T MELA-AU 19 57642404 57642404 single base substitution G A downstream_gene_variant MELA-AU 19 57642404 57642404 single base substitution G A synonymous_variant L787L 2361G>A MELA-AU 19 57642615 57642615 single base substitution G A downstream_gene_variant MELA-AU 19 57642615 57642615 single base substitution G A missense_variant D858N 2572G>A MELA-AU 19 57642635 57642635 single base substitution C T downstream_gene_variant MELA-AU 19 57642635 57642635 single base substitution C T synonymous_variant I864I 2592C>T MELA-AU 19 57642654 57642654 single base substitution G A downstream_gene_variant MELA-AU 19 57642654 57642654 single base substitution G A missense_variant E871K 2611G>A MELA-AU 19 57642720 57642720 single base substitution A G downstream_gene_variant MELA-AU 19 57642720 57642720 single base substitution A G missense_variant R893G 2677A>G MELA-AU 19 57642767 57642767 single base substitution C T downstream_gene_variant MELA-AU 19 57642767 57642767 single base substitution C T synonymous_variant I908I 2724C>T MELA-AU 19 57642768 57642769 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 57642768 57642769 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P909F 2725CC>TT MELA-AU 19 57642783 57642783 single base substitution G A downstream_gene_variant MELA-AU 19 57642783 57642783 single base substitution G A missense_variant E914K 2740G>A MELA-AU 19 57642793 57642793 single base substitution C T downstream_gene_variant MELA-AU 19 57642793 57642793 single base substitution C T missense_variant S917F 2750C>T MELA-AU 19 57642834 57642834 single base substitution C T 3_prime_UTR_variant MELA-AU 19 57642834 57642834 single base substitution C T downstream_gene_variant MELA-AU 19 57642864 57642864 single base substitution C T 3_prime_UTR_variant MELA-AU 19 57642864 57642864 single base substitution C T downstream_gene_variant MELA-AU 19 57642912 57642912 single base substitution C T 3_prime_UTR_variant MELA-AU 19 57642912 57642912 single base substitution C T downstream_gene_variant MELA-AU 19 57643014 57643014 single base substitution C T 3_prime_UTR_variant MELA-AU 19 57643014 57643014 single base substitution C T downstream_gene_variant MELA-AU 19 57643282 57643282 single base substitution G A 3_prime_UTR_variant MELA-AU 19 57643282 57643282 single base substitution G A downstream_gene_variant MELA-AU 19 57643324 57643324 single base substitution G A downstream_gene_variant MELA-AU 19 57643373 57643373 single base substitution C T downstream_gene_variant MELA-AU 19 57643394 57643394 single base substitution C T downstream_gene_variant MELA-AU 19 57643405 57643405 single base substitution C T downstream_gene_variant MELA-AU 19 57643416 57643416 single base substitution G A downstream_gene_variant MELA-AU 19 57643476 57643476 single base substitution G A downstream_gene_variant MELA-AU 19 57643520 57643520 single base substitution G A downstream_gene_variant MELA-AU 19 57643632 57643632 single base substitution G A downstream_gene_variant MELA-AU 19 57644195 57644195 single base substitution G A downstream_gene_variant MELA-AU 19 57644314 57644314 single base substitution G A downstream_gene_variant MELA-AU 19 57644319 57644319 single base substitution G A downstream_gene_variant MELA-AU 19 57644359 57644359 single base substitution G A downstream_gene_variant MELA-AU 19 57644406 57644406 single base substitution C T downstream_gene_variant MELA-AU 19 57644682 57644682 single base substitution T C downstream_gene_variant MELA-AU 19 57644805 57644805 single base substitution G A downstream_gene_variant MELA-AU 19 57644817 57644817 single base substitution G A downstream_gene_variant MELA-AU 19 57644859 57644859 single base substitution G A downstream_gene_variant MELA-AU 19 57644860 57644860 single base substitution G A downstream_gene_variant MELA-AU 19 57644964 57644964 single base substitution G A downstream_gene_variant MELA-AU 19 57644972 57644973 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 57645026 57645026 single base substitution A G downstream_gene_variant MELA-AU 19 57645037 57645037 single base substitution T G downstream_gene_variant MELA-AU 19 57645056 57645056 single base substitution G A downstream_gene_variant MELA-AU 19 57645076 57645076 single base substitution C T downstream_gene_variant MELA-AU 19 57645236 57645236 single base substitution C T downstream_gene_variant MELA-AU 19 57645366 57645366 single base substitution G A downstream_gene_variant MELA-AU 19 57645393 57645393 single base substitution G A downstream_gene_variant MELA-AU 19 57645395 57645395 single base substitution G A downstream_gene_variant MELA-AU 19 57645454 57645454 single base substitution A T downstream_gene_variant MELA-AU 19 57645610 57645610 single base substitution T A downstream_gene_variant MELA-AU 19 57645670 57645670 single base substitution G A downstream_gene_variant MELA-AU 19 57645868 57645868 single base substitution G A downstream_gene_variant MELA-AU 19 57645870 57645870 single base substitution A G downstream_gene_variant MELA-AU 19 57645917 57645917 single base substitution G A downstream_gene_variant MELA-AU 19 57645918 57645918 single base substitution G A downstream_gene_variant MELA-AU 19 57646143 57646143 single base substitution G A downstream_gene_variant MELA-AU 19 57646272 57646272 single base substitution A G downstream_gene_variant MELA-AU 19 57646302 57646302 single base substitution C T downstream_gene_variant MELA-AU 19 57646368 57646368 single base substitution G A downstream_gene_variant MELA-AU 19 57646468 57646468 single base substitution G A downstream_gene_variant MELA-AU 19 57646552 57646552 single base substitution G A downstream_gene_variant MELA-AU 19 57646553 57646553 single base substitution G A downstream_gene_variant MELA-AU 19 57646571 57646571 single base substitution G A downstream_gene_variant MELA-AU 19 57646845 57646845 single base substitution G A downstream_gene_variant MELA-AU 19 57646991 57646991 single base substitution G A downstream_gene_variant MELA-AU 19 57647256 57647256 single base substitution C T downstream_gene_variant MELA-AU 19 57647271 57647271 single base substitution G A downstream_gene_variant MELA-AU 19 57647718 57647718 single base substitution G A downstream_gene_variant MELA-AU 19 57647885 57647885 single base substitution C T downstream_gene_variant MELA-AU 19 57647889 57647889 single base substitution G A downstream_gene_variant MELA-AU 19 57647916 57647916 single base substitution C A downstream_gene_variant MELA-AU 19 57647925 57647925 single base substitution G A downstream_gene_variant MELA-AU 19 57647951 57647951 single base substitution G A downstream_gene_variant MELA-AU 19 57647986 57647986 single base substitution C T downstream_gene_variant MELA-AU 19 57648000 57648000 single base substitution C T downstream_gene_variant MELA-AU 19 57648079 57648079 single base substitution C T downstream_gene_variant MELA-AU 19 57648109 57648109 single base substitution G A downstream_gene_variant MELA-AU 19 57648146 57648146 single base substitution G A downstream_gene_variant MELA-AU 19 57648169 57648169 single base substitution G A downstream_gene_variant MELA-AU 19 57648271 57648271 single base substitution C T downstream_gene_variant MELA-AU 19 57648287 57648287 single base substitution C T downstream_gene_variant OV-AU 19 57630852 57630852 single base substitution G A intron_variant OV-AU 19 57630852 57630852 single base substitution G A upstream_gene_variant OV-AU 19 57632114 57632114 single base substitution C G intron_variant OV-AU 19 57637065 57637065 single base substitution T C intron_variant OV-AU 19 57637065 57637065 single base substitution T C upstream_gene_variant OV-AU 19 57641012 57641012 single base substitution T A downstream_gene_variant OV-AU 19 57641012 57641012 single base substitution T A synonymous_variant I323I 969T>A OV-AU 19 57641957 57641957 single base substitution G A downstream_gene_variant OV-AU 19 57641957 57641957 single base substitution G A synonymous_variant R638R 1914G>A OV-AU 19 57642417 57642417 single base substitution C T downstream_gene_variant OV-AU 19 57642417 57642417 single base substitution C T missense_variant P792S 2374C>T OV-AU 19 57643222 57643222 single base substitution G A 3_prime_UTR_variant OV-AU 19 57643222 57643222 single base substitution G A downstream_gene_variant OV-AU 19 57643929 57643929 single base substitution G T downstream_gene_variant OV-AU 19 57646969 57646969 single base substitution T C downstream_gene_variant PACA-AU 19 57628510 57628510 single base substitution A G upstream_gene_variant PACA-AU 19 57628957 57628957 single base substitution A C upstream_gene_variant PACA-AU 19 57630742 57630742 single base substitution C T intron_variant PACA-AU 19 57630742 57630742 single base substitution C T upstream_gene_variant PACA-AU 19 57631228 57631228 single base substitution G A intron_variant PACA-AU 19 57631228 57631228 single base substitution G A upstream_gene_variant PACA-AU 19 57631494 57631494 single base substitution C A 5_prime_UTR_variant PACA-AU 19 57631494 57631494 single base substitution C A intron_variant PACA-AU 19 57633003 57633003 single base substitution C G intron_variant PACA-AU 19 57637059 57637059 single base substitution C A intron_variant PACA-AU 19 57637059 57637059 single base substitution C A upstream_gene_variant PACA-AU 19 57638925 57638925 single base substitution C A intron_variant PACA-AU 19 57638925 57638925 single base substitution C A upstream_gene_variant PACA-AU 19 57639461 57639461 single base substitution C A intron_variant PACA-AU 19 57639461 57639461 single base substitution C A upstream_gene_variant PACA-AU 19 57639504 57639504 single base substitution C T intron_variant PACA-AU 19 57639504 57639504 single base substitution C T upstream_gene_variant PACA-AU 19 57640746 57640746 single base substitution A T downstream_gene_variant PACA-AU 19 57640746 57640746 single base substitution A T missense_variant N235Y 703A>T PACA-AU 19 57641808 57641808 single base substitution G T downstream_gene_variant PACA-AU 19 57641808 57641808 single base substitution G T missense_variant D589Y 1765G>T PACA-AU 19 57645103 57645103 single base substitution A G downstream_gene_variant PACA-AU 19 57646095 57646095 single base substitution A G downstream_gene_variant PACA-CA 19 57625937 57625937 single base substitution C T upstream_gene_variant PACA-CA 19 57626743 57626743 single base substitution T C upstream_gene_variant PACA-CA 19 57626753 57626753 single base substitution G A upstream_gene_variant PACA-CA 19 57628540 57628540 single base substitution T A upstream_gene_variant PACA-CA 19 57630556 57630556 single base substitution G A 5_prime_UTR_variant PACA-CA 19 57630556 57630556 single base substitution G A upstream_gene_variant PACA-CA 19 57630569 57630569 single base substitution G A 5_prime_UTR_variant PACA-CA 19 57630569 57630569 single base substitution G A upstream_gene_variant PACA-CA 19 57630822 57630822 single base substitution G A intron_variant PACA-CA 19 57630822 57630822 single base substitution G A upstream_gene_variant PACA-CA 19 57631158 57631158 single base substitution G A intron_variant PACA-CA 19 57631158 57631158 single base substitution G A upstream_gene_variant PACA-CA 19 57631233 57631233 single base substitution G A intron_variant PACA-CA 19 57631233 57631233 single base substitution G A upstream_gene_variant PACA-CA 19 57632323 57632323 single base substitution C T intron_variant PACA-CA 19 57636044 57636044 single base substitution T A intron_variant PACA-CA 19 57636044 57636044 single base substitution T A upstream_gene_variant PACA-CA 19 57636993 57636993 single base substitution C A intron_variant PACA-CA 19 57636993 57636993 single base substitution C A upstream_gene_variant PACA-CA 19 57636994 57636994 single base substitution C T intron_variant PACA-CA 19 57636994 57636994 single base substitution C T upstream_gene_variant PACA-CA 19 57638496 57638496 single base substitution C A intron_variant PACA-CA 19 57638496 57638496 single base substitution C A upstream_gene_variant PACA-CA 19 57639299 57639299 single base substitution C A intron_variant PACA-CA 19 57639299 57639299 single base substitution C A upstream_gene_variant PACA-CA 19 57639365 57639365 single base substitution C T intron_variant PACA-CA 19 57639365 57639365 single base substitution C T upstream_gene_variant PACA-CA 19 57639643 57639643 single base substitution T G intron_variant PACA-CA 19 57639643 57639643 single base substitution T G upstream_gene_variant PACA-CA 19 57639903 57639903 single base substitution G C intron_variant PACA-CA 19 57639903 57639903 single base substitution G C upstream_gene_variant PACA-CA 19 57640716 57640716 single base substitution G A downstream_gene_variant PACA-CA 19 57640716 57640716 single base substitution G A missense_variant G225R 673G>A PACA-CA 19 57640916 57640916 single base substitution A G downstream_gene_variant PACA-CA 19 57640916 57640916 single base substitution A G synonymous_variant G291G 873A>G PACA-CA 19 57641631 57641631 single base substitution T C downstream_gene_variant PACA-CA 19 57641631 57641631 single base substitution T C missense_variant Y530H 1588T>C PACA-CA 19 57641680 57641680 single base substitution A C downstream_gene_variant PACA-CA 19 57641680 57641680 single base substitution A C missense_variant K546T 1637A>C PACA-CA 19 57642540 57642540 single base substitution G A downstream_gene_variant PACA-CA 19 57642540 57642540 single base substitution G A missense_variant G833R 2497G>A PACA-CA 19 57643509 57643509 single base substitution G A downstream_gene_variant PACA-CA 19 57644371 57644371 single base substitution C T downstream_gene_variant PACA-CA 19 57645004 57645004 single base substitution G C downstream_gene_variant PAEN-AU 19 57643493 57643493 single base substitution C A downstream_gene_variant PAEN-IT 19 57643820 57643820 single base substitution G A downstream_gene_variant PBCA-DE 19 57627183 57627183 single base substitution C T upstream_gene_variant PBCA-DE 19 57630852 57630852 single base substitution G A intron_variant PBCA-DE 19 57630852 57630852 single base substitution G A upstream_gene_variant PBCA-DE 19 57632874 57632874 single base substitution T C intron_variant PBCA-DE 19 57632897 57632897 single base substitution A G intron_variant PBCA-DE 19 57636949 57636949 single base substitution G C intron_variant PBCA-DE 19 57636949 57636949 single base substitution G C upstream_gene_variant PRAD-CA 19 57632243 57632243 single base substitution C T intron_variant PRAD-CA 19 57632290 57632290 single base substitution C T intron_variant PRAD-CA 19 57639841 57639841 single base substitution G A intron_variant PRAD-CA 19 57639841 57639841 single base substitution G A upstream_gene_variant PRAD-CA 19 57645123 57645123 single base substitution A G downstream_gene_variant PRAD-UK 19 57630536 57630536 single base substitution C T 5_prime_UTR_variant PRAD-UK 19 57630536 57630536 single base substitution C T upstream_gene_variant PRAD-UK 19 57631334 57631334 single base substitution G A intron_variant PRAD-UK 19 57631334 57631334 single base substitution G A upstream_gene_variant PRAD-UK 19 57633507 57633507 single base substitution G A intron_variant PRAD-UK 19 57634460 57634460 single base substitution C A intron_variant PRAD-UK 19 57647703 57647703 single base substitution G C downstream_gene_variant PRAD-UK 19 57647889 57647889 single base substitution G A downstream_gene_variant PRAD-US 19 57640708 57640708 single base substitution T C downstream_gene_variant PRAD-US 19 57640708 57640708 single base substitution T C missense_variant L222S 665T>C READ-US 19 57640913 57640913 single base substitution G T downstream_gene_variant READ-US 19 57640913 57640913 single base substitution G T missense_variant L290F 870G>T READ-US 19 57641066 57641066 single base substitution C A downstream_gene_variant READ-US 19 57641066 57641066 single base substitution C A missense_variant F341L 1023C>A READ-US 19 57641593 57641593 single base substitution A G downstream_gene_variant READ-US 19 57641593 57641593 single base substitution A G missense_variant N517S 1550A>G READ-US 19 57646640 57646640 single base substitution T G downstream_gene_variant READ-US 19 57646889 57646889 single base substitution A C downstream_gene_variant RECA-EU 19 57626012 57626012 single base substitution T A upstream_gene_variant RECA-EU 19 57626321 57626321 single base substitution G T upstream_gene_variant RECA-EU 19 57629674 57629674 single base substitution A G upstream_gene_variant RECA-EU 19 57630769 57630769 single base substitution T A intron_variant RECA-EU 19 57630769 57630769 single base substitution T A upstream_gene_variant RECA-EU 19 57630830 57630830 single base substitution G A intron_variant RECA-EU 19 57630830 57630830 single base substitution G A upstream_gene_variant RECA-EU 19 57637914 57637914 single base substitution A C intron_variant RECA-EU 19 57637914 57637914 single base substitution A C upstream_gene_variant RECA-EU 19 57638011 57638011 single base substitution T C intron_variant RECA-EU 19 57638011 57638011 single base substitution T C upstream_gene_variant RECA-EU 19 57638926 57638926 single base substitution C T intron_variant RECA-EU 19 57638926 57638926 single base substitution C T upstream_gene_variant RECA-EU 19 57645138 57645138 single base substitution G T downstream_gene_variant RECA-EU 19 57645320 57645320 single base substitution T A downstream_gene_variant RECA-EU 19 57647011 57647011 single base substitution A G downstream_gene_variant RECA-EU 19 57647288 57647288 single base substitution G C downstream_gene_variant SKCA-BR 19 57627035 57627035 single base substitution C T upstream_gene_variant SKCA-BR 19 57627363 57627363 single base substitution C T upstream_gene_variant SKCA-BR 19 57627822 57627822 single base substitution C T upstream_gene_variant SKCA-BR 19 57628870 57628870 single base substitution A G upstream_gene_variant SKCA-BR 19 57628896 57628896 single base substitution C T upstream_gene_variant SKCA-BR 19 57629905 57629905 single base substitution G A upstream_gene_variant SKCA-BR 19 57630685 57630685 single base substitution G A intron_variant SKCA-BR 19 57630685 57630685 single base substitution G A upstream_gene_variant SKCA-BR 19 57631364 57631364 single base substitution C T intron_variant SKCA-BR 19 57631364 57631364 single base substitution C T upstream_gene_variant SKCA-BR 19 57631379 57631379 single base substitution G A intron_variant SKCA-BR 19 57631379 57631379 single base substitution G A upstream_gene_variant SKCA-BR 19 57631404 57631404 single base substitution C T intron_variant SKCA-BR 19 57631404 57631404 single base substitution C T upstream_gene_variant SKCA-BR 19 57631844 57631844 single base substitution C T intron_variant SKCA-BR 19 57633475 57633475 single base substitution G A intron_variant SKCA-BR 19 57633608 57633608 single base substitution C T intron_variant SKCA-BR 19 57633609 57633609 single base substitution C T intron_variant SKCA-BR 19 57634288 57634288 single base substitution G A intron_variant SKCA-BR 19 57636972 57636972 single base substitution T C intron_variant SKCA-BR 19 57636972 57636972 single base substitution T C upstream_gene_variant SKCA-BR 19 57637307 57637307 single base substitution C T intron_variant SKCA-BR 19 57637307 57637307 single base substitution C T upstream_gene_variant SKCA-BR 19 57637439 57637439 single base substitution C T intron_variant SKCA-BR 19 57637439 57637439 single base substitution C T upstream_gene_variant SKCA-BR 19 57637973 57637973 single base substitution C T intron_variant SKCA-BR 19 57637973 57637973 single base substitution C T upstream_gene_variant SKCA-BR 19 57638429 57638429 single base substitution T A intron_variant SKCA-BR 19 57638429 57638429 single base substitution T A upstream_gene_variant SKCA-BR 19 57638459 57638459 single base substitution G A intron_variant SKCA-BR 19 57638459 57638459 single base substitution G A upstream_gene_variant SKCA-BR 19 57639014 57639014 single base substitution C T intron_variant SKCA-BR 19 57639014 57639014 single base substitution C T upstream_gene_variant SKCA-BR 19 57639380 57639380 single base substitution G T intron_variant SKCA-BR 19 57639380 57639380 single base substitution G T upstream_gene_variant SKCA-BR 19 57640146 57640146 single base substitution G A downstream_gene_variant SKCA-BR 19 57640146 57640146 single base substitution G A missense_variant E35K 103G>A SKCA-BR 19 57640376 57640376 single base substitution G A downstream_gene_variant SKCA-BR 19 57640376 57640376 single base substitution G A missense_variant M111I 333G>A SKCA-BR 19 57641015 57641015 single base substitution C T downstream_gene_variant SKCA-BR 19 57641015 57641015 single base substitution C T synonymous_variant P324P 972C>T SKCA-BR 19 57641724 57641724 single base substitution G A downstream_gene_variant SKCA-BR 19 57641724 57641724 single base substitution G A missense_variant E561K 1681G>A SKCA-BR 19 57641869 57641869 single base substitution A T downstream_gene_variant SKCA-BR 19 57641869 57641869 single base substitution A T missense_variant D609V 1826A>T SKCA-BR 19 57641996 57641996 single base substitution G A downstream_gene_variant SKCA-BR 19 57641996 57641996 single base substitution G A synonymous_variant L651L 1953G>A SKCA-BR 19 57642143 57642143 single base substitution C T downstream_gene_variant SKCA-BR 19 57642143 57642143 single base substitution C T synonymous_variant F700F 2100C>T SKCA-BR 19 57642335 57642335 single base substitution A T downstream_gene_variant SKCA-BR 19 57642335 57642335 single base substitution A T synonymous_variant T764T 2292A>T SKCA-BR 19 57642914 57642914 single base substitution C T 3_prime_UTR_variant SKCA-BR 19 57642914 57642914 single base substitution C T downstream_gene_variant SKCA-BR 19 57644095 57644096 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 19 57645209 57645209 single base substitution G A downstream_gene_variant SKCA-BR 19 57646222 57646222 single base substitution G A downstream_gene_variant SKCA-BR 19 57646302 57646302 single base substitution C T downstream_gene_variant SKCA-BR 19 57646362 57646362 single base substitution C T downstream_gene_variant SKCA-BR 19 57647242 57647242 single base substitution C T downstream_gene_variant SKCA-BR 19 57647356 57647356 single base substitution C T downstream_gene_variant SKCA-BR 19 57648058 57648058 single base substitution G C downstream_gene_variant SKCA-BR 19 57648256 57648256 single base substitution C T downstream_gene_variant SKCM-US 19 57640051 57640051 single base substitution C T missense_variant S3F 8C>T SKCM-US 19 57640096 57640096 single base substitution G A downstream_gene_variant SKCM-US 19 57640096 57640096 single base substitution G A missense_variant G18E 53G>A SKCM-US 19 57640177 57640177 single base substitution G A downstream_gene_variant SKCM-US 19 57640177 57640177 single base substitution G A missense_variant G45E 134G>A SKCM-US 19 57640194 57640194 single base substitution T C downstream_gene_variant SKCM-US 19 57640194 57640194 single base substitution T C missense_variant F51L 151T>C SKCM-US 19 57640197 57640197 single base substitution C T downstream_gene_variant SKCM-US 19 57640197 57640197 single base substitution C T stop_gained Q52* 154C>T SKCM-US 19 57640306 57640306 single base substitution C T downstream_gene_variant SKCM-US 19 57640306 57640306 single base substitution C T missense_variant S88F 263C>T SKCM-US 19 57640373 57640373 single base substitution C T downstream_gene_variant SKCM-US 19 57640373 57640373 single base substitution C T synonymous_variant P110P 330C>T SKCM-US 19 57640376 57640376 single base substitution G A downstream_gene_variant SKCM-US 19 57640376 57640376 single base substitution G A missense_variant M111I 333G>A SKCM-US 19 57640381 57640381 single base substitution C T downstream_gene_variant SKCM-US 19 57640381 57640381 single base substitution C T missense_variant S113F 338C>T SKCM-US 19 57640386 57640386 single base substitution G A downstream_gene_variant SKCM-US 19 57640386 57640386 single base substitution G A missense_variant D115N 343G>A SKCM-US 19 57640389 57640389 single base substitution G A downstream_gene_variant SKCM-US 19 57640389 57640389 single base substitution G A missense_variant D116N 346G>A SKCM-US 19 57640452 57640452 single base substitution A G downstream_gene_variant SKCM-US 19 57640452 57640452 single base substitution A G missense_variant I137V 409A>G SKCM-US 19 57640501 57640501 single base substitution C T downstream_gene_variant SKCM-US 19 57640501 57640501 single base substitution C T missense_variant S153L 458C>T SKCM-US 19 57640539 57640539 single base substitution G A downstream_gene_variant SKCM-US 19 57640539 57640539 single base substitution G A missense_variant G166S 496G>A SKCM-US 19 57640569 57640569 single base substitution G A downstream_gene_variant SKCM-US 19 57640569 57640569 single base substitution G A missense_variant D176N 526G>A SKCM-US 19 57640595 57640595 single base substitution G A downstream_gene_variant SKCM-US 19 57640595 57640595 single base substitution G A synonymous_variant L184L 552G>A SKCM-US 19 57640685 57640685 single base substitution G A downstream_gene_variant SKCM-US 19 57640685 57640685 single base substitution G A synonymous_variant E214E 642G>A SKCM-US 19 57640713 57640713 single base substitution C T downstream_gene_variant SKCM-US 19 57640713 57640713 single base substitution C T missense_variant L224F 670C>T SKCM-US 19 57640749 57640749 single base substitution C T downstream_gene_variant SKCM-US 19 57640749 57640749 single base substitution C T missense_variant P236S 706C>T SKCM-US 19 57640800 57640800 single base substitution G A downstream_gene_variant SKCM-US 19 57640800 57640800 single base substitution G A missense_variant G253S 757G>A SKCM-US 19 57640915 57640915 single base substitution G A downstream_gene_variant SKCM-US 19 57640915 57640915 single base substitution G A missense_variant G291E 872G>A SKCM-US 19 57640948 57640948 single base substitution C T downstream_gene_variant SKCM-US 19 57640948 57640948 single base substitution C T missense_variant S302L 905C>T SKCM-US 19 57640962 57640962 single base substitution C T downstream_gene_variant SKCM-US 19 57640962 57640962 single base substitution C T missense_variant P307S 919C>T SKCM-US 19 57640963 57640963 single base substitution C T downstream_gene_variant SKCM-US 19 57640963 57640963 single base substitution C T missense_variant P307L 920C>T SKCM-US 19 57640966 57640966 single base substitution C T downstream_gene_variant SKCM-US 19 57640966 57640966 single base substitution C T missense_variant S308F 923C>T SKCM-US 19 57640991 57640991 single base substitution A C downstream_gene_variant SKCM-US 19 57640991 57640991 single base substitution A C missense_variant Q316H 948A>C SKCM-US 19 57640998 57640998 single base substitution C T downstream_gene_variant SKCM-US 19 57640998 57640998 single base substitution C T missense_variant P319S 955C>T SKCM-US 19 57641002 57641002 single base substitution G A downstream_gene_variant SKCM-US 19 57641002 57641002 single base substitution G A stop_gained W320* 959G>A SKCM-US 19 57641013 57641013 single base substitution C T downstream_gene_variant SKCM-US 19 57641013 57641013 single base substitution C T missense_variant P324S 970C>T SKCM-US 19 57641025 57641025 single base substitution C T downstream_gene_variant SKCM-US 19 57641025 57641025 single base substitution C T missense_variant L328F 982C>T SKCM-US 19 57641084 57641084 single base substitution G A downstream_gene_variant SKCM-US 19 57641084 57641084 single base substitution G A synonymous_variant K347K 1041G>A SKCM-US 19 57641091 57641091 single base substitution T A downstream_gene_variant SKCM-US 19 57641091 57641091 single base substitution T A missense_variant L350I 1048T>A SKCM-US 19 57641114 57641114 single base substitution C T downstream_gene_variant SKCM-US 19 57641114 57641114 single base substitution C T synonymous_variant V357V 1071C>T SKCM-US 19 57641153 57641153 single base substitution G A downstream_gene_variant SKCM-US 19 57641153 57641153 single base substitution G A synonymous_variant Q370Q 1110G>A SKCM-US 19 57641207 57641207 single base substitution G A downstream_gene_variant SKCM-US 19 57641207 57641207 single base substitution G A missense_variant M388I 1164G>A SKCM-US 19 57641248 57641248 single base substitution G A downstream_gene_variant SKCM-US 19 57641248 57641248 single base substitution G A missense_variant G402E 1205G>A SKCM-US 19 57641322 57641322 single base substitution A G downstream_gene_variant SKCM-US 19 57641322 57641322 single base substitution A G missense_variant N427D 1279A>G SKCM-US 19 57641395 57641395 single base substitution A C downstream_gene_variant SKCM-US 19 57641395 57641395 single base substitution A C missense_variant N451T 1352A>C SKCM-US 19 57641411 57641411 single base substitution C T downstream_gene_variant SKCM-US 19 57641411 57641411 single base substitution C T synonymous_variant I456I 1368C>T SKCM-US 19 57641421 57641421 single base substitution C T downstream_gene_variant SKCM-US 19 57641421 57641421 single base substitution C T stop_gained Q460* 1378C>T SKCM-US 19 57641439 57641439 single base substitution C T downstream_gene_variant SKCM-US 19 57641439 57641439 single base substitution C T missense_variant P466S 1396C>T SKCM-US 19 57641478 57641478 single base substitution G A downstream_gene_variant SKCM-US 19 57641478 57641478 single base substitution G A missense_variant E479K 1435G>A SKCM-US 19 57641516 57641516 single base substitution G A downstream_gene_variant SKCM-US 19 57641516 57641516 single base substitution G A synonymous_variant Q491Q 1473G>A SKCM-US 19 57641622 57641622 single base substitution G A downstream_gene_variant SKCM-US 19 57641622 57641622 single base substitution G A missense_variant E527K 1579G>A SKCM-US 19 57641670 57641670 single base substitution G A downstream_gene_variant SKCM-US 19 57641670 57641670 single base substitution G A missense_variant E543K 1627G>A SKCM-US 19 57641786 57641786 single base substitution G A downstream_gene_variant SKCM-US 19 57641786 57641786 single base substitution G A missense_variant M581I 1743G>A SKCM-US 19 57641808 57641808 single base substitution G A downstream_gene_variant SKCM-US 19 57641808 57641808 single base substitution G A missense_variant D589N 1765G>A SKCM-US 19 57641952 57641952 single base substitution G A downstream_gene_variant SKCM-US 19 57641952 57641952 single base substitution G A missense_variant D637N 1909G>A SKCM-US 19 57642007 57642007 single base substitution G A downstream_gene_variant SKCM-US 19 57642007 57642007 single base substitution G A missense_variant G655E 1964G>A SKCM-US 19 57642045 57642045 single base substitution A G downstream_gene_variant SKCM-US 19 57642045 57642045 single base substitution A G missense_variant K668E 2002A>G SKCM-US 19 57642176 57642176 single base substitution C T downstream_gene_variant SKCM-US 19 57642176 57642176 single base substitution C T synonymous_variant S711S 2133C>T SKCM-US 19 57642220 57642220 single base substitution G A downstream_gene_variant SKCM-US 19 57642220 57642220 single base substitution G A missense_variant G726E 2177G>A SKCM-US 19 57642237 57642237 single base substitution G T downstream_gene_variant SKCM-US 19 57642237 57642237 single base substitution G T stop_gained E732* 2194G>T SKCM-US 19 57642372 57642372 single base substitution C T downstream_gene_variant SKCM-US 19 57642372 57642372 single base substitution C T stop_gained Q777* 2329C>T SKCM-US 19 57642421 57642421 single base substitution G A downstream_gene_variant SKCM-US 19 57642421 57642421 single base substitution G A missense_variant G793E 2378G>A SKCM-US 19 57642485 57642485 single base substitution G A downstream_gene_variant SKCM-US 19 57642485 57642485 single base substitution G A synonymous_variant V814V 2442G>A SKCM-US 19 57642498 57642498 single base substitution C T downstream_gene_variant SKCM-US 19 57642498 57642498 single base substitution C T missense_variant P819S 2455C>T SKCM-US 19 57642539 57642539 single base substitution C T downstream_gene_variant SKCM-US 19 57642539 57642539 single base substitution C T synonymous_variant I832I 2496C>T SKCM-US 19 57642599 57642599 single base substitution C T downstream_gene_variant SKCM-US 19 57642599 57642599 single base substitution C T synonymous_variant A852A 2556C>T SKCM-US 19 57642603 57642603 single base substitution T C downstream_gene_variant SKCM-US 19 57642603 57642603 single base substitution T C missense_variant F854L 2560T>C SKCM-US 19 57642615 57642615 single base substitution G A downstream_gene_variant SKCM-US 19 57642615 57642615 single base substitution G A missense_variant D858N 2572G>A SKCM-US 19 57642699 57642699 single base substitution G A downstream_gene_variant SKCM-US 19 57642699 57642699 single base substitution G A missense_variant G886R 2656G>A SKCM-US 19 57642767 57642767 single base substitution C T downstream_gene_variant SKCM-US 19 57642767 57642767 single base substitution C T synonymous_variant I908I 2724C>T SKCM-US 19 57642775 57642775 single base substitution G A downstream_gene_variant SKCM-US 19 57642775 57642775 single base substitution G A missense_variant G911E 2732G>A SKCM-US 19 57642776 57642776 single base substitution G A downstream_gene_variant SKCM-US 19 57642776 57642776 single base substitution G A synonymous_variant G911G 2733G>A SKCM-US 19 57646302 57646302 single base substitution C T downstream_gene_variant SKCM-US 19 57646329 57646329 single base substitution C T downstream_gene_variant SKCM-US 19 57646362 57646362 single base substitution C T downstream_gene_variant SKCM-US 19 57646378 57646378 single base substitution C T downstream_gene_variant SKCM-US 19 57646415 57646415 single base substitution C T downstream_gene_variant SKCM-US 19 57646454 57646454 single base substitution C T downstream_gene_variant SKCM-US 19 57646462 57646462 single base substitution C T downstream_gene_variant SKCM-US 19 57646475 57646475 single base substitution C T downstream_gene_variant SKCM-US 19 57646480 57646480 single base substitution G A downstream_gene_variant SKCM-US 19 57646505 57646505 single base substitution G A downstream_gene_variant SKCM-US 19 57646515 57646515 single base substitution C T downstream_gene_variant SKCM-US 19 57646543 57646543 single base substitution C T downstream_gene_variant SKCM-US 19 57646552 57646552 single base substitution G A downstream_gene_variant SKCM-US 19 57646553 57646553 single base substitution G A downstream_gene_variant SKCM-US 19 57646628 57646628 single base substitution C T downstream_gene_variant SKCM-US 19 57646636 57646636 single base substitution G A downstream_gene_variant SKCM-US 19 57646651 57646651 single base substitution C T downstream_gene_variant SKCM-US 19 57646682 57646682 single base substitution C T downstream_gene_variant SKCM-US 19 57646757 57646757 single base substitution G A downstream_gene_variant SKCM-US 19 57646787 57646787 single base substitution G A downstream_gene_variant SKCM-US 19 57646858 57646858 single base substitution C T downstream_gene_variant SKCM-US 19 57646872 57646872 single base substitution G A downstream_gene_variant SKCM-US 19 57646923 57646923 single base substitution G A downstream_gene_variant SKCM-US 19 57646987 57646987 single base substitution G A downstream_gene_variant SKCM-US 19 57647019 57647019 single base substitution C T downstream_gene_variant SKCM-US 19 57647025 57647025 single base substitution T C downstream_gene_variant SKCM-US 19 57647093 57647093 single base substitution G A downstream_gene_variant SKCM-US 19 57647152 57647152 single base substitution G A downstream_gene_variant SKCM-US 19 57647171 57647171 single base substitution T C downstream_gene_variant SKCM-US 19 57647197 57647197 single base substitution T G downstream_gene_variant SKCM-US 19 57647422 57647422 single base substitution C T downstream_gene_variant SKCM-US 19 57648268 57648268 single base substitution C T downstream_gene_variant SKCM-US 19 57648286 57648286 single base substitution C T downstream_gene_variant SKCM-US 19 57648289 57648289 single base substitution T A downstream_gene_variant SKCM-US 19 57648291 57648291 single base substitution C T downstream_gene_variant STAD-US 19 57640239 57640239 insertion of <=200bp - A downstream_gene_variant STAD-US 19 57640239 57640239 insertion of <=200bp - A frameshift_variant K66K? STAD-US 19 57641113 57641113 single base substitution T C downstream_gene_variant STAD-US 19 57641113 57641113 single base substitution T C missense_variant V357A 1070T>C STAD-US 19 57641212 57641212 single base substitution A C downstream_gene_variant STAD-US 19 57641212 57641212 single base substitution A C missense_variant K390T 1169A>C STAD-US 19 57641380 57641380 single base substitution T C downstream_gene_variant STAD-US 19 57641380 57641380 single base substitution T C missense_variant L446P 1337T>C STAD-US 19 57641483 57641483 single base substitution A C downstream_gene_variant STAD-US 19 57641483 57641483 single base substitution A C missense_variant E480D 1440A>C STAD-US 19 57641627 57641627 single base substitution A G downstream_gene_variant STAD-US 19 57641627 57641627 single base substitution A G synonymous_variant Q528Q 1584A>G STAD-US 19 57641676 57641676 single base substitution A G downstream_gene_variant STAD-US 19 57641676 57641676 single base substitution A G missense_variant T545A 1633A>G STAD-US 19 57641825 57641825 single base substitution C T downstream_gene_variant STAD-US 19 57641825 57641825 single base substitution C T synonymous_variant P594P 1782C>T STAD-US 19 57642249 57642249 single base substitution C A downstream_gene_variant STAD-US 19 57642249 57642249 single base substitution C A missense_variant Q736K 2206C>A STAD-US 19 57642751 57642751 single base substitution C T downstream_gene_variant STAD-US 19 57642751 57642751 single base substitution C T missense_variant T903I 2708C>T STAD-US 19 57646387 57646387 deletion of <=200bp T - downstream_gene_variant STAD-US 19 57646555 57646555 deletion of <=200bp T - downstream_gene_variant STAD-US 19 57646555 57646555 insertion of <=200bp - T downstream_gene_variant STAD-US 19 57647283 57647283 single base substitution A G downstream_gene_variant STAD-US 19 57647341 57647341 single base substitution C T downstream_gene_variant STAD-US 19 57647393 57647393 single base substitution G A downstream_gene_variant STAD-US 19 57647457 57647457 deletion of <=200bp T - downstream_gene_variant STAD-US 19 57648269 57648269 single base substitution T G downstream_gene_variant THCA-SA 19 57635417 57635417 single base substitution G A 5_prime_UTR_variant THCA-SA 19 57635417 57635417 single base substitution G A upstream_gene_variant UCEC-US 19 57640286 57640286 single base substitution C A downstream_gene_variant UCEC-US 19 57640286 57640286 single base substitution C A missense_variant F81L 243C>A UCEC-US 19 57640462 57640462 single base substitution A C downstream_gene_variant UCEC-US 19 57640462 57640462 single base substitution A C missense_variant K140T 419A>C UCEC-US 19 57640547 57640547 single base substitution G A downstream_gene_variant UCEC-US 19 57640547 57640547 single base substitution G A synonymous_variant K168K 504G>A UCEC-US 19 57640638 57640638 single base substitution T C downstream_gene_variant UCEC-US 19 57640638 57640638 single base substitution T C missense_variant S199P 595T>C UCEC-US 19 57640712 57640712 single base substitution A G downstream_gene_variant UCEC-US 19 57640712 57640712 single base substitution A G synonymous_variant K223K 669A>G UCEC-US 19 57640818 57640818 single base substitution G A downstream_gene_variant UCEC-US 19 57640818 57640818 single base substitution G A missense_variant E259K 775G>A UCEC-US 19 57641066 57641066 single base substitution C A downstream_gene_variant UCEC-US 19 57641066 57641066 single base substitution C A missense_variant F341L 1023C>A UCEC-US 19 57641241 57641241 single base substitution G T downstream_gene_variant UCEC-US 19 57641241 57641241 single base substitution G T stop_gained E400* 1198G>T UCEC-US 19 57641296 57641296 single base substitution A C downstream_gene_variant UCEC-US 19 57641296 57641296 single base substitution A C missense_variant K418T 1253A>C UCEC-US 19 57641437 57641437 single base substitution T C downstream_gene_variant UCEC-US 19 57641437 57641437 single base substitution T C missense_variant L465P 1394T>C UCEC-US 19 57641466 57641466 single base substitution C A downstream_gene_variant UCEC-US 19 57641466 57641466 single base substitution C A missense_variant L475I 1423C>A UCEC-US 19 57641471 57641471 single base substitution C A downstream_gene_variant UCEC-US 19 57641471 57641471 single base substitution C A missense_variant F476L 1428C>A UCEC-US 19 57641656 57641656 single base substitution C A downstream_gene_variant UCEC-US 19 57641656 57641656 single base substitution C A missense_variant S538Y 1613C>A UCEC-US 19 57641907 57641907 single base substitution C A downstream_gene_variant UCEC-US 19 57641907 57641907 single base substitution C A missense_variant L622M 1864C>A UCEC-US 19 57641940 57641940 single base substitution G A downstream_gene_variant UCEC-US 19 57641940 57641940 single base substitution G A missense_variant V633I 1897G>A UCEC-US 19 57641963 57641963 single base substitution C T downstream_gene_variant UCEC-US 19 57641963 57641963 single base substitution C T synonymous_variant I640I 1920C>T UCEC-US 19 57641964 57641964 single base substitution G A downstream_gene_variant UCEC-US 19 57641964 57641964 single base substitution G A missense_variant G641S 1921G>A UCEC-US 19 57642036 57642036 single base substitution G T downstream_gene_variant UCEC-US 19 57642036 57642036 single base substitution G T missense_variant D665Y 1993G>T UCEC-US 19 57642298 57642298 single base substitution C A downstream_gene_variant UCEC-US 19 57642298 57642298 single base substitution C A missense_variant P752H 2255C>A UCEC-US 19 57642512 57642512 single base substitution C T downstream_gene_variant UCEC-US 19 57642512 57642512 single base substitution C T synonymous_variant Y823Y 2469C>T UCEC-US 19 57642590 57642590 single base substitution G T downstream_gene_variant UCEC-US 19 57642590 57642590 single base substitution G T missense_variant Q849H 2547G>T UCEC-US 19 57646558 57646558 single base substitution T G downstream_gene_variant UCEC-US 19 57646580 57646580 single base substitution C A downstream_gene_variant UCEC-US 19 57646651 57646651 single base substitution C T downstream_gene_variant UCEC-US 19 57646709 57646709 single base substitution C A downstream_gene_variant UCEC-US 19 57646877 57646877 single base substitution C A downstream_gene_variant UCEC-US 19 57646993 57646993 single base substitution G T downstream_gene_variant UCEC-US 19 57647093 57647093 single base substitution G A downstream_gene_variant UCEC-US 19 57647341 57647341 single base substitution C T downstream_gene_variant UCEC-US 19 57647398 57647398 single base substitution C A downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LUAD-NYU330 COSM373809 c.1765G>T p.D589Y Substitution - Missense 19:57130440-57130440 + TCGA-CJ-5684-01 COSM475363 c.2495T>C p.I832T Substitution - Missense 19:57131170-57131170 + ICC010T COSM1002085 c.1920C>T p.I640I Substitution - coding silent 19:57130595-57130595 + TCGA-AZ-4315-01 COSM1396946 c.1588T>G p.Y530D Substitution - Missense 19:57130263-57130263 + TCGA-AX-A05Z-01 COSM1002086 c.1921G>A p.G641S Substitution - Missense 19:57130596-57130596 + TCGA-EE-A181-06 COSM3540327 c.2733G>A p.G911G Substitution - coding silent 19:57131408-57131408 + PT35 COSM5914213 c.1649C>T p.P550L Substitution - Missense 19:57130324-57130324 + TCGA-B0-5705-01 COSM3363041 c.2703T>C p.P901P Substitution - coding silent 19:57131378-57131378 + TCGA-46-3765-01 COSM714260 c.1469A>C p.K490T Substitution - Missense 19:57130144-57130144 + PT37 COSM5390918 c.382G>A p.E128K Substitution - Missense 19:57129057-57129057 + NB07C COSM1236557 c.980C>G p.A327G Substitution - Missense 19:57129655-57129655 + LUAD-NYU575 COSM375031 c.1909G>T p.D637Y Substitution - Missense 19:57130584-57130584 + CHC1592T COSM4791355 c.205C>A p.Q69K Substitution - Missense 19:57128880-57128880 + Pat_01_A COSM5856890 c.1996G>A p.G666R Substitution - Missense 19:57130671-57130671 + TCGA-39-5027-01 COSM714272 c.31C>T p.Q11* Substitution - Nonsense 19:57128706-57128706 + YUPAT COSM1712966 c.103G>A p.E35K Substitution - Missense 19:57128778-57128778 + LS174T COSM2971677 c.335A>C p.K112T Substitution - Missense 19:57129010-57129010 + CSCC-57-T COSM4563182 c.961G>A p.E321K Substitution - Missense 19:57129636-57129636 + TCGA-GF-A6C9-06 COSM4900621 c.970C>T p.P324S Substitution - Missense 19:57129645-57129645 + TCGA-BR-8297-01 COSM4081972 c.1337T>C p.L446P Substitution - Missense 19:57130012-57130012 + PT36 COSM5916785 c.1786G>A p.E596K Substitution - Missense 19:57130461-57130461 + 234 COSM3731447 c.2729_2730insG p.E912fs*5 Insertion - Frameshift 19:57131404-57131405 + TCGA-HE-7130-01 COSM3990331 c.1144G>C p.D382H Substitution - Missense 19:57129819-57129819 + CSCC-20-T COSM3540284 c.134G>A p.G45E Substitution - Missense 19:57128809-57128809 + TCGA-B5-A11E-01 COSM1002073 c.669A>G p.K223K Substitution - coding silent 19:57129344-57129344 + TCGA-CG-5721-01 COSM4081975 c.1633A>G p.T545A Substitution - Missense 19:57130308-57130308 + 103639 COSM96264 c.1353T>C p.N451N Substitution - coding silent 19:57130028-57130028 + TCGA-RP-A693-06 COSM4895602 c.8C>T p.S3F Substitution - Missense 19:57128683-57128683 + LUAD-NYU1219 COSM369992 c.1324G>T p.G442C Substitution - Missense 19:57129999-57129999 + YUKAT COSM5390922 c.1861G>A p.D621N Substitution - Missense 19:57130536-57130536 + TCGA-AZ-4315-01 COSM1396942 c.784C>T p.H262Y Substitution - Missense 19:57129459-57129459 + LUAD-E00443 COSM391556 c.51_52insG p.M19fs*3 Insertion - Frameshift 19:57128726-57128727 + ESCC-008T COSM3938325 c.1837G>A p.A613T Substitution - Missense 19:57130512-57130512 + P07-360 COSM248241 c.2571C>T p.N857N Substitution - coding silent 19:57131246-57131246 + TCGA-D1-A16Y-01 COSM264601 c.243C>A p.F81L Substitution - Missense 19:57128918-57128918 + SNUH_G45_S1 COSM4001003 c.1756G>A p.E586K Substitution - Missense 19:57130431-57130431 + EWS502 COSM4581482 c.1450T>G p.Y484D Substitution - Missense 19:57130125-57130125 + NPC26F COSM4995974 c.2224A>G p.I742V Substitution - Missense 19:57130899-57130899 + TCGA-51-4081-01 COSM714267 c.529G>T p.V177L Substitution - Missense 19:57129204-57129204 + S00356 COSM318277 c.893C>A p.A298E Substitution - Missense 19:57129568-57129568 + 112287 COSM95449 c.1679G>A p.C560Y Substitution - Missense 19:57130354-57130354 + TCGA-BS-A0TA-01 COSM1002089 c.2469C>T p.Y823Y Substitution - coding silent 19:57131144-57131144 + CHC801T COSM4953385 c.1885G>T p.E629* Substitution - Nonsense 19:57130560-57130560 + D3 COSM5006772 c.2529C>T p.S843S Substitution - coding silent 19:57131204-57131204 + TCGA-FW-A3R5-06 COSM3893719 c.2378G>A p.G793E Substitution - Missense 19:57131053-57131053 + TCGA-EE-A2MD-06 COSM3540299 c.872G>A p.G291E Substitution - Missense 19:57129547-57129547 + TCGA-D9-A1JW-06 COSM3540315 c.1743G>A p.M581I Substitution - Missense 19:57130418-57130418 + PT50 COSM5937838 c.2171C>T p.P724L Substitution - Missense 19:57130846-57130846 + YUDIALE COSM1712971 c.1966G>A p.D656N Substitution - Missense 19:57130641-57130641 + RK243_C01 COSM4779869 c.2743G>A p.G915S Substitution - Missense 19:57131418-57131418 + TCGA-BR-4279-01 COSM4081976 c.1782C>T p.P594P Substitution - coding silent 19:57130457-57130457 + 587284 COSM1232016 c.1492C>T p.H498Y Substitution - Missense 19:57130167-57130167 + 61 COSM5741757 c.844C>T p.Q282* Substitution - Nonsense 19:57129519-57129519 + TCGA-66-2768-01 COSM714264 c.851A>T p.Q284L Substitution - Missense 19:57129526-57129526 + TCGA-D3-A3ML-06 COSM1681417 c.923C>T p.S308F Substitution - Missense 19:57129598-57129598 + LAU149 COSM235549 c.1686C>T p.V562V Substitution - coding silent 19:57130361-57130361 + TCGA-D3-A51T-06 COSM2971720 c.2177G>A p.G726E Substitution - Missense 19:57130852-57130852 + TCGA-D9-A6EC-06 COSM3540292 c.458C>T p.S153L Substitution - Missense 19:57129133-57129133 + 100879 COSM95448 c.659G>C p.R220T Substitution - Missense 19:57129334-57129334 + TCGA-F4-6570-01 COSM1396939 c.195_196insA p.R68fs*18 Insertion - Frameshift 19:57128870-57128871 + TCGA-EE-A182-06 COSM3540289 c.338C>T p.S113F Substitution - Missense 19:57129013-57129013 + BCM397T COSM4951739 c.824C>A p.P275H Substitution - Missense 19:57129499-57129499 + TCGA-AA-3715-01 COSM270527 c.2550G>A p.K850K Substitution - coding silent 19:57131225-57131225 + AOCS-147-1-1 COSM4127939 c.2374C>T p.P792S Substitution - Missense 19:57131049-57131049 + PCSI_0090_Pa_X COSM3378857 c.873A>G p.G291G Substitution - coding silent 19:57129548-57129548 + HCC174 COSM3707445 c.2334G>A p.K778K Substitution - coding silent 19:57131009-57131009 + TCGA-EE-A29G-06 COSM3540306 c.1048T>A p.L350I Substitution - Missense 19:57129723-57129723 + 392 COSM4428218 c.1616C>G p.S539C Substitution - Missense 19:57130291-57130291 + TCGA-AP-A05N-01 COSM1002084 c.1897G>A p.V633I Substitution - Missense 19:57130572-57130572 + TCGA-AH-6544-01 COSM1564969 c.870G>T p.L290F Substitution - Missense 19:57129545-57129545 + 202_T COSM3960595 c.1079C>T p.A360V Substitution - Missense 19:57129754-57129754 + HCC1395 COSM27235 c.1362C>G p.L454L Substitution - coding silent 19:57130037-57130037 + TCGA-B0-5705-01 COSM3363039 c.2695C>A p.R899R Substitution - coding silent 19:57131370-57131370 + 1_RESISTANT COSM1720946 c.863C>T p.P288L Substitution - Missense 19:57129538-57129538 + S02292 COSM5687687 c.1895T>A p.L632* Substitution - Nonsense 19:57130570-57130570 + BD239T COSM5497313 c.2059C>A p.Q687K Substitution - Missense 19:57130734-57130734 + 2039 COSM1645112 c.92A>C p.Q31P Substitution - Missense 19:57128767-57128767 + CN-AML-CR-62-Dx COSM3757307 c.2055G>A p.V685V Substitution - coding silent 19:57130730-57130730 + HCT-116 COSM1681418 c.1309A>T p.I437F Substitution - Missense 19:57129984-57129984 + 2492721 COSM5723053 c.1397C>T p.P466L Substitution - Missense 19:57130072-57130072 + TCGA-AP-A0LM-01 COSM1002080 c.1423C>A p.L475I Substitution - Missense 19:57130098-57130098 + LUAD-NYU263 COSM372206 c.2650C>A p.H884N Substitution - Missense 19:57131325-57131325 + TCGA-22-5489-01 COSM714257 c.2567A>G p.Y856C Substitution - Missense 19:57131242-57131242 + TCGA-D3-A51T-06 COSM1712973 c.2572G>A p.D858N Substitution - Missense 19:57131247-57131247 + 2492713 COSM5607193 c.1770C>T p.S590S Substitution - coding silent 19:57130445-57130445 + YUMER COSM1712970 c.1397C>A p.P466H Substitution - Missense 19:57130072-57130072 + C089 COSM5543588 c.164A>G p.N55S Substitution - Missense 19:57128839-57128839 + 4537_T COSM258335 c.2750C>A p.S917Y Substitution - Missense 19:57131425-57131425 + TCGA-14-0813 COSM2154755 c.1711T>A p.S571T Substitution - Missense 19:57130386-57130386 + T231 COSM4739749 c.1796A>C p.K599T Substitution - Missense 19:57130471-57130471 + TCGA-D5-6928-01 COSM1396940 c.477G>A p.K159K Substitution - coding silent 19:57129152-57129152 + CHC801T COSM4953385 c.1885G>T p.E629* Substitution - Nonsense 19:57130560-57130560 + ZZUFHECRKL-G060T COSM5438436 c.2081A>G p.Y694C Substitution - Missense 19:57130756-57130756 + 079T COSM1730740 c.2655T>A p.N885K Substitution - Missense 19:57131330-57131330 + BCM397T COSM4951739 c.824C>A p.P275H Substitution - Missense 19:57129499-57129499 + TCGA-66-2756-01 COSM714261 c.1270G>T p.V424F Substitution - Missense 19:57129945-57129945 + TCGA-BS-A0UV-01 COSM1002088 c.2255C>A p.P752H Substitution - Missense 19:57130930-57130930 + CDGLIV0707A0251_T COSM5038691 c.855delG p.F287fs*10 Deletion - Frameshift 19:57129530-57129530 + LUAD-E00443 COSM363859 c.1391C>G p.P464R Substitution - Missense 19:57130066-57130066 + CSCC-27-T COSM4563182 c.961G>A p.E321K Substitution - Missense 19:57129636-57129636 + PCSI_0509_Pa_P_526 COSM4962026 c.673G>A p.G225R Substitution - Missense 19:57129348-57129348 + YUMOBER COSM5390923 c.1975C>T p.L659F Substitution - Missense 19:57130650-57130650 + Pat_66_A COSM3797597 c.2035G>A p.E679K Substitution - Missense 19:57130710-57130710 + Case4 COSM1579277 c.875A>T p.N292I Substitution - Missense 19:57129550-57129550 + TCGA-EE-A2MR-06 COSM3540326 c.2732G>A p.G911E Substitution - Missense 19:57131407-57131407 + TCGA-EE-A181-06 COSM3540287 c.330C>T p.P110P Substitution - coding silent 19:57129005-57129005 + 08-P8005 COSM4581483 c.2316A>G p.T772T Substitution - coding silent 19:57130991-57130991 + TCGA-EB-A44N-01 COSM3540311 c.1378C>T p.Q460* Substitution - Nonsense 19:57130053-57130053 + ESCC-D16 COSM5045617 c.1891G>A p.E631K Substitution - Missense 19:57130566-57130566 + LAU63 COSM234322 c.493C>T p.Q165* Substitution - Nonsense 19:57129168-57129168 + TCGA-AP-A0LI-01 COSM1002075 c.998C>G p.T333S Substitution - Missense 19:57129673-57129673 + LUAD-CHTN-MAD06-00668 COSM359388 c.949G>T p.G317C Substitution - Missense 19:57129624-57129624 + TCGA-AN-A0XN-01 COSM440462 c.2389A>C p.I797L Substitution - Missense 19:57131064-57131064 + AOCS-114-1-8 COSM4127938 c.1914G>A p.R638R Substitution - coding silent 19:57130589-57130589 + YUOMEGA COSM5390925 c.2212A>T p.I738F Substitution - Missense 19:57130887-57130887 + LUAD-F00121 COSM365744 c.971C>A p.P324H Substitution - Missense 19:57129646-57129646 + ESO-1059 COSM1270071 c.396T>C p.T132T Substitution - coding silent 19:57129071-57129071 + ccRCC-77 COSM1664916 c.1753T>C p.S585P Substitution - Missense 19:57130428-57130428 + RK119_C01 COSM3743166 c.1631G>A p.S544N Substitution - Missense 19:57130306-57130306 + TCGA-B0-5107-01 COSM475362 c.775G>T p.E259* Substitution - Nonsense 19:57129450-57129450 + TCGA-AA-A00N-01 COSM278037 c.882T>G p.C294W Substitution - Missense 19:57129557-57129557 + YUGAFFE COSM1712973 c.2572G>A p.D858N Substitution - Missense 19:57131247-57131247 + ESCC-240T COSM3938324 c.623A>T p.K208M Substitution - Missense 19:57129298-57129298 + YUTRAIN COSM5390924 c.1990G>A p.E664K Substitution - Missense 19:57130665-57130665 + TCGA-D3-A51T-06 COSM3540290 c.346G>A p.D116N Substitution - Missense 19:57129021-57129021 + sysucc-311T COSM5464782 c.624G>T p.K208N Substitution - Missense 19:57129299-57129299 + C086 COSM3540307 c.1205G>A p.G402E Substitution - Missense 19:57129880-57129880 + TCGA-DK-A2I4-01 COSM3797596 c.1210G>A p.E404K Substitution - Missense 19:57129885-57129885 + TCGA-BS-A0UF-01 COSM1002078 c.1253A>C p.K418T Substitution - Missense 19:57129928-57129928 + CSCC-55-T COSM4469508 c.1601C>T p.S534F Substitution - Missense 19:57130276-57130276 + TCGA-DG-A2KK-01 COSM4828411 c.471G>C p.V157V Substitution - coding silent 19:57129146-57129146 + CSCC-44-T COSM4539658 c.2718G>A p.G906G Substitution - coding silent 19:57131393-57131393 + 86793 COSM95450 c.1723A>C p.S575R Substitution - Missense 19:57130398-57130398 + TCGA-AP-A056-01 COSM1002082 c.1613C>A p.S538Y Substitution - Missense 19:57130288-57130288 + WM3211 COSM2971673 c.263C>T p.S88F Substitution - Missense 19:57128938-57128938 + TCGA-ER-A193-06 COSM3540303 c.955C>T p.P319S Substitution - Missense 19:57129630-57129630 + TCGA-ER-A193-06 COSM3893718 c.2002A>G p.K668E Substitution - Missense 19:57130677-57130677 + Au8 COSM5607193 c.1770C>T p.S590S Substitution - coding silent 19:57130445-57130445 + PT55 COSM1712972 c.2158G>A p.E720K Substitution - Missense 19:57130833-57130833 + TCGA-CK-4950-01 COSM1396943 c.887T>G p.M296R Substitution - Missense 19:57129562-57129562 + YUSCA COSM5390926 c.2252C>T p.P751L Substitution - Missense 19:57130927-57130927 + CSCC-20-T COSM1396939 c.195_196insA p.R68fs*18 Insertion - Frameshift 19:57128870-57128871 + T2269 COSM4739751 c.2662T>G p.F888V Substitution - Missense 19:57131337-57131337 + TCGA-C5-A2M2-01 COSM4837705 c.1581G>T p.E527D Substitution - Missense 19:57130256-57130256 + 2492712 COSM5607193 c.1770C>T p.S590S Substitution - coding silent 19:57130445-57130445 + L18 COSM5369344 c.1658G>A p.S553N Substitution - Missense 19:57130333-57130333 + TCGA-AD-5900-01 COSM1396944 c.1063delA p.V357fs*21 Deletion - Frameshift 19:57129738-57129738 + ESCC_82 COSM4336687 c.1433_1435delAAG p.E481delE Deletion - In frame 19:57130108-57130110 + S02209 COSM5675248 c.2668G>A p.E890K Substitution - Missense 19:57131343-57131343 + ESCC_BICR_034T COSM5443516 c.2684C>A p.A895E Substitution - Missense 19:57131359-57131359 + TCGA-D1-A16J-01 COSM1002074 c.775G>A p.E259K Substitution - Missense 19:57129450-57129450 + PT48 COSM1712966 c.103G>A p.E35K Substitution - Missense 19:57128778-57128778 + TCGA-B0-5705-01 COSM3363040 c.2696G>T p.R899L Substitution - Missense 19:57131371-57131371 + TCGA-FW-A3R5-06 COSM3893720 c.2442G>A p.V814V Substitution - coding silent 19:57131117-57131117 + CSCC-11-T COSM4533705 c.2007G>A p.L669L Substitution - coding silent 19:57130682-57130682 + YUOMEGA COSM5390921 c.1804G>A p.D602N Substitution - Missense 19:57130479-57130479 + 2492714 COSM5607193 c.1770C>T p.S590S Substitution - coding silent 19:57130445-57130445 + TCGA-51-4079-01 COSM714268 c.382G>T p.E128* Substitution - Nonsense 19:57129057-57129057 + TCGA-EE-A2M5-06 COSM3540293 c.496G>A p.G166S Substitution - Missense 19:57129171-57129171 + 2_RESISTANT COSM1722929 c.934G>A p.D312N Substitution - Missense 19:57129609-57129609 + TCGA-AA-A010-01 COSM264601 c.243C>A p.F81L Substitution - Missense 19:57128918-57128918 + 61 COSM5741756 c.749C>T p.A250V Substitution - Missense 19:57129424-57129424 + TCGA-FR-A3YN-06 COSM3540325 c.2724C>T p.I908I Substitution - coding silent 19:57131399-57131399 + 8036161 COSM373809 c.1765G>T p.D589Y Substitution - Missense 19:57130440-57130440 + CSCC-27-T COSM4549405 c.471G>A p.V157V Substitution - coding silent 19:57129146-57129146 + HCC35 COSM1612920 c.1518C>T p.V506V Substitution - coding silent 19:57130193-57130193 + CSCC-49-T COSM226834 c.2530G>A p.D844N Substitution - Missense 19:57131205-57131205 + LAU149 COSM235550 c.1687C>T p.L563L Substitution - coding silent 19:57130362-57130362 + ESCC_99 COSM5637760 c.1251C>A p.T417T Substitution - coding silent 19:57129926-57129926 + TCGA-D5-6931-01 COSM1396941 c.542A>G p.E181G Substitution - Missense 19:57129217-57129217 + YULAN COSM440460 c.211C>T p.H71Y Substitution - Missense 19:57128886-57128886 + J52_T COSM3960594 c.1043G>A p.R348K Substitution - Missense 19:57129718-57129718 + TCGA-EE-A2M5-06 COSM3540285 c.151T>C p.F51L Substitution - Missense 19:57128826-57128826 + TCGA-D3-A5GN-06 COSM3540325 c.2724C>T p.I908I Substitution - coding silent 19:57131399-57131399 + TCGA-C5-A1BK-01 COSM4826290 c.1645C>T p.L549F Substitution - Missense 19:57130320-57130320 + YURUS COSM1712967 c.478G>A p.G160R Substitution - Missense 19:57129153-57129153 + TCGA-18-3409-01 COSM714256 c.2640C>T p.F880F Substitution - coding silent 19:57131315-57131315 + TCGA-DK-A2I4-01 COSM3797595 c.1045G>A p.E349K Substitution - Missense 19:57129720-57129720 + TCGA-C5-A7UH-01 COSM4856610 c.1123G>T p.E375* Substitution - Nonsense 19:57129798-57129798 + ESCC_BICR_008T COSM226834 c.2530G>A p.D844N Substitution - Missense 19:57131205-57131205 + T2258 COSM248241 c.2571C>T p.N857N Substitution - coding silent 19:57131246-57131246 + TCGA-EE-A2GC-06 COSM3540324 c.2656G>A p.G886R Substitution - Missense 19:57131331-57131331 + NPC38F COSM3960594 c.1043G>A p.R348K Substitution - Missense 19:57129718-57129718 + 2521259 COSM5723053 c.1397C>T p.P466L Substitution - Missense 19:57130072-57130072 + TCGA-E2-A14S-01 COSM440461 c.328C>T p.P110S Substitution - Missense 19:57129003-57129003 + TCGA-EE-A2MT-06 COSM3540298 c.757G>A p.G253S Substitution - Missense 19:57129432-57129432 + 3N59-VS-3T59 COSM4984206 c.1849C>A p.Q617K Substitution - Missense 19:57130524-57130524 + TCGA-14-0813-01 COSM2154755 c.1711T>A p.S571T Substitution - Missense 19:57130386-57130386 + sysucc-826T COSM264602 c.1118C>T p.A373V Substitution - Missense 19:57129793-57129793 + SC_9109 COSM288702 c.1716G>T p.E572D Substitution - Missense 19:57130391-57130391 + CSCC-29-T COSM4570341 c.259T>C p.L87L Substitution - coding silent 19:57128934-57128934 + YUOTHO COSM3540292 c.458C>T p.S153L Substitution - Missense 19:57129133-57129133 + TCGA-FW-A3R5-06 COSM2971714 c.1964G>A p.G655E Substitution - Missense 19:57130639-57130639 + TCGA-EE-A181-06 COSM3540284 c.134G>A p.G45E Substitution - Missense 19:57128809-57128809 + 2492723 COSM5723053 c.1397C>T p.P466L Substitution - Missense 19:57130072-57130072 + YUNEON COSM1712969 c.1265G>T p.C422F Substitution - Missense 19:57129940-57129940 + YUDIALE COSM1712972 c.2158G>A p.E720K Substitution - Missense 19:57130833-57130833 + H1672 COSM316404 c.497G>C p.G166A Substitution - Missense 19:57129172-57129172 + CSCC-6-T COSM4528391 c.1533G>A p.L511L Substitution - coding silent 19:57130208-57130208 + TCGA-FW-A3R5-06 COSM3893717 c.1627G>A p.E543K Substitution - Missense 19:57130302-57130302 + 2492729 COSM5726856 c.1509C>T p.L503L Substitution - coding silent 19:57130184-57130184 + TCGA-BF-A3DL-01 COSM4904604 c.905C>T p.S302L Substitution - Missense 19:57129580-57129580 + TCGA-DK-A2I4-01 COSM3797594 c.829G>A p.D277N Substitution - Missense 19:57129504-57129504 + LS411 COSM2971734 c.2653A>T p.N885Y Substitution - Missense 19:57131328-57131328 + TCGA-ER-A193-06 COSM3540290 c.346G>A p.D116N Substitution - Missense 19:57129021-57129021 + TCGA-AF-3400-01 COSM287756 c.1659T>C p.S553S Substitution - coding silent 19:57130334-57130334 + HCC35T COSM1612920 c.1518C>T p.V506V Substitution - coding silent 19:57130193-57130193 + Au9 COSM5607663 c.971C>T p.P324L Substitution - Missense 19:57129646-57129646 + HCC2998 COSM1681419 c.1355A>C p.N452T Substitution - Missense 19:57130030-57130030 + LS180 COSM2971677 c.335A>C p.K112T Substitution - Missense 19:57129010-57129010 + 587376 COSM1232020 c.2693C>A p.S898Y Substitution - Missense 19:57131368-57131368 + TCGA-AP-A051-01 COSM1002071 c.504G>A p.K168K Substitution - coding silent 19:57129179-57129179 + SS6003125 COSM3414101 c.2515G>C p.G839R Substitution - Missense 19:57131190-57131190 + TCGA-AG-A002-01 COSM264601 c.243C>A p.F81L Substitution - Missense 19:57128918-57128918 + Pat_01_B COSM5856890 c.1996G>A p.G666R Substitution - Missense 19:57130671-57130671 + TCGA-FS-A1Z3-06 COSM3540286 c.154C>T p.Q52* Substitution - Nonsense 19:57128829-57128829 + PT48 COSM5933957 c.2452G>A p.D818N Substitution - Missense 19:57131127-57131127 + BD72T COSM5513593 c.2476A>G p.I826V Substitution - Missense 19:57131151-57131151 + HCC153T COSM5823260 c.525T>A p.S175S Substitution - coding silent 19:57129200-57129200 + 40M COSM5586978 c.2100C>T p.F700F Substitution - coding silent 19:57130775-57130775 + SC_9008 COSM267733 c.196delA p.R68fs*7 Deletion - Frameshift 19:57128871-57128871 + CSCC-27-T COSM4461712 c.1217C>T p.S406L Substitution - Missense 19:57129892-57129892 + TCGA-BR-6452-01 COSM4081970 c.1070T>C p.V357A Substitution - Missense 19:57129745-57129745 + CSCC-60-T COSM4536450 c.22G>A p.G8R Substitution - Missense 19:57128697-57128697 + TCGA-EE-A2MS-06 COSM3540313 c.1435G>A p.E479K Substitution - Missense 19:57130110-57130110 + TCGA-D3-A5GN-06 COSM3540291 c.409A>G p.I137V Substitution - Missense 19:57129084-57129084 + TCGA-39-5031-01 COSM714265 c.649G>C p.E217Q Substitution - Missense 19:57129324-57129324 + 2492720 COSM3540286 c.154C>T p.Q52* Substitution - Nonsense 19:57128829-57128829 + T2269 COSM4739750 c.2286A>G p.E762E Substitution - coding silent 19:57130961-57130961 + TCGA-D3-A2JF-06 COSM3540300 c.919C>T p.P307S Substitution - Missense 19:57129594-57129594 + BD121T COSM5515744 c.2640C>A p.F880L Substitution - Missense 19:57131315-57131315 + LOXIMVI COSM1681417 c.923C>T p.S308F Substitution - Missense 19:57129598-57129598 + 86791 COSM95685 c.39G>A p.W13* Substitution - Nonsense 19:57128714-57128714 + YUSIPU COSM3540317 c.1909G>A p.D637N Substitution - Missense 19:57130584-57130584 + TCGA-FS-A1ZZ-06 COSM3540318 c.2133C>T p.S711S Substitution - coding silent 19:57130808-57130808 + T1232 COSM4336687 c.1433_1435delAAG p.E481delE Deletion - In frame 19:57130108-57130110 + TCGA-BH-A0B6-01 COSM3835918 c.1285G>C p.E429Q Substitution - Missense 19:57129960-57129960 + PT33 COSM5909791 c.956C>T p.P319L Substitution - Missense 19:57129631-57129631 + 2290930 COSM4440541 c.2368G>A p.D790N Substitution - Missense 19:57131043-57131043 + TCGA-C5-A7UH-01 COSM4856903 c.1420G>C p.D474H Substitution - Missense 19:57130095-57130095 + 587376 COSM1232018 c.649G>T p.E217* Substitution - Nonsense 19:57129324-57129324 + TCGA-G3-A3CI-01 COSM4939250 c.7T>A p.S3T Substitution - Missense 19:57128682-57128682 + TCGA-F5-6814-01 COSM3423263 c.1550A>G p.N517S Substitution - Missense 19:57130225-57130225 + CHC603T COSM3668366 c.1371C>T p.N457N Substitution - coding silent 19:57130046-57130046 + TCGA-39-5027-01 COSM714271 c.41G>A p.S14N Substitution - Missense 19:57128716-57128716 + TCGA-F5-6814-01 COSM1002076 c.1023C>A p.F341L Substitution - Missense 19:57129698-57129698 + TCGA-CU-A3YL-01 COSM3797597 c.2035G>A p.E679K Substitution - Missense 19:57130710-57130710 + TCGA-D1-A16X-01 COSM1002070 c.419A>C p.K140T Substitution - Missense 19:57129094-57129094 + TCGA-D3-A2JF-06 COSM3540320 c.2329C>T p.Q777* Substitution - Nonsense 19:57131004-57131004 + TCGA-D9-A6EC-06 COSM4400255 c.1473G>A p.Q491Q Substitution - coding silent 19:57130148-57130148 + HT29 COSM2971670 c.186T>C p.L62L Substitution - coding silent 19:57128861-57128861 + TCGA-D3-A51J-06 COSM3540297 c.706C>T p.P236S Substitution - Missense 19:57129381-57129381 + T3225 COSM2971679 c.476A>G p.K159R Substitution - Missense 19:57129151-57129151 + 3N05-VS-3T05 COSM4978767 c.148A>C p.I50L Substitution - Missense 19:57128823-57128823 + PCSI_0325_Pa_P_526 COSM3734614 c.2497G>A p.G833R Substitution - Missense 19:57131172-57131172 + TCGA-EE-A3JB-06 COSM4898102 c.982C>T p.L328F Substitution - Missense 19:57129657-57129657 + TCGA-EE-A2M5-06 COSM3540304 c.959G>A p.W320* Substitution - Nonsense 19:57129634-57129634 + AOCS-056-1-X COSM4127937 c.969T>A p.I323I Substitution - coding silent 19:57129644-57129644 + CSCC-49-T COSM714272 c.31C>T p.Q11* Substitution - Nonsense 19:57128706-57128706 + HCC174T COSM3707445 c.2334G>A p.K778K Substitution - coding silent 19:57131009-57131009 + ESCC_25 COSM1396940 c.477G>A p.K159K Substitution - coding silent 19:57129152-57129152 + TCGA-CG-4306-01 COSM4081977 c.2206C>A p.Q736K Substitution - Missense 19:57130881-57130881 + HN_62854 COSM128450 c.2451G>T p.G817G Substitution - coding silent 19:57131126-57131126 + 2492723 COSM3540286 c.154C>T p.Q52* Substitution - Nonsense 19:57128829-57128829 + TCGA-DA-A3F8-06 COSM3540288 c.333G>A p.M111I Substitution - Missense 19:57129008-57129008 + BD114T COSM5504612 c.2335G>A p.A779T Substitution - Missense 19:57131010-57131010 + TCGA-66-2791-01 COSM714254 c.2712G>T p.Q904H Substitution - Missense 19:57131387-57131387 + TCGA-CA-6717-01 COSM1396950 c.2046T>C p.L682L Substitution - coding silent 19:57130721-57130721 + TCGA-D3-A5GU-06 COSM3540314 c.1579G>A p.E527K Substitution - Missense 19:57130254-57130254 + TCGA-EE-A29N-06 COSM3540299 c.872G>A p.G291E Substitution - Missense 19:57129547-57129547 + Au1 COSM5597859 c.2170C>T p.P724S Substitution - Missense 19:57130845-57130845 + T578 COSM4739746 c.929C>T p.A310V Substitution - Missense 19:57129604-57129604 + Au4 COSM5605306 c.727C>T p.L243F Substitution - Missense 19:57129402-57129402 + Pat_08_B COSM5856889 c.390C>A p.D130E Substitution - Missense 19:57129065-57129065 + 2492722 COSM5723053 c.1397C>T p.P466L Substitution - Missense 19:57130072-57130072 + 2492720 COSM5723053 c.1397C>T p.P466L Substitution - Missense 19:57130072-57130072 + TCGA-BS-A0UF-01 COSM1002079 c.1394T>C p.L465P Substitution - Missense 19:57130069-57130069 + TCGA-HU-A4GF-01 COSM4081973 c.1440A>C p.E480D Substitution - Missense 19:57130115-57130115 + TCGA-34-2600-01 COSM714270 c.57G>C p.M19I Substitution - Missense 19:57128732-57128732 + 10_5283 COSM1645113 c.2479A>G p.S827G Substitution - Missense 19:57131154-57131154 + TCGA-GN-A266-06 COSM1712973 c.2572G>A p.D858N Substitution - Missense 19:57131247-57131247 + TCGA-EB-A3Y7-01 COSM3540295 c.552G>A p.L184L Substitution - coding silent 19:57129227-57129227 + ESO-859 COSM1240622 c.1468A>G p.K490E Substitution - Missense 19:57130143-57130143 + T2269 COSM1002081 c.1428C>A p.F476L Substitution - Missense 19:57130103-57130103 + CSCC-27-T COSM4536319 c.228G>A p.L76L Substitution - coding silent 19:57128903-57128903 + TCGA-FS-A1ZA-06 COSM3540299 c.872G>A p.G291E Substitution - Missense 19:57129547-57129547 + TCGA-AA-A010-01 COSM286391 c.670C>T p.L224F Substitution - Missense 19:57129345-57129345 + PD24219a COSM5796007 c.1328A>C p.H443P Substitution - Missense 19:57130003-57130003 + TCGA-61-1900-01 COSM1326133 c.1056G>A p.G352G Substitution - coding silent 19:57129731-57129731 + T3262 COSM4739745 c.145A>G p.R49G Substitution - Missense 19:57128820-57128820 + PT46 COSM5929978 c.2186G>A p.G729E Substitution - Missense 19:57130861-57130861 + pfg108T COSM4755997 c.2215G>T p.E739* Substitution - Nonsense 19:57130890-57130890 + J36_T COSM3960596 c.2440G>T p.V814L Substitution - Missense 19:57131115-57131115 + 2_PRE-TREATMENT COSM1722929 c.934G>A p.D312N Substitution - Missense 19:57129609-57129609 + PT50 COSM5937837 c.2611G>A p.E871K Substitution - Missense 19:57131286-57131286 + PT08_1 COSM5894053 c.1973C>T p.S658F Substitution - Missense 19:57130648-57130648 + TCGA-BS-A0UV-01 COSM1002077 c.1198G>T p.E400* Substitution - Nonsense 19:57129873-57129873 + 587376 COSM1232017 c.271G>T p.D91Y Substitution - Missense 19:57128946-57128946 + CSCC-31-T COSM3540284 c.134G>A p.G45E Substitution - Missense 19:57128809-57128809 + TCGA-D3-A2JF-06 COSM3540317 c.1909G>A p.D637N Substitution - Missense 19:57130584-57130584 + 2206 COSM1396944 c.1063delA p.V357fs*21 Deletion - Frameshift 19:57129738-57129738 + S00356 COSM318277 c.893C>A p.A298E Substitution - Missense 19:57129568-57129568 + TCGA-EE-A3JH-06 COSM3540292 c.458C>T p.S153L Substitution - Missense 19:57129133-57129133 + ME011T COSM224584 c.689C>T p.T230I Substitution - Missense 19:57129364-57129364 + TCGA-AX-A05Z-01 COSM1002087 c.1993G>T p.D665Y Substitution - Missense 19:57130668-57130668 + RK165_C01 COSM1631128 c.830A>G p.D277G Substitution - Missense 19:57129505-57129505 + TCGA-DA-A3F8-06 COSM1712973 c.2572G>A p.D858N Substitution - Missense 19:57131247-57131247 + 388 COSM3724111 c.2280C>T p.A760A Substitution - coding silent 19:57130955-57130955 + TCGA-EE-A2GU-06 COSM3540294 c.526G>A p.D176N Substitution - Missense 19:57129201-57129201 + ESCC_BICR_025T COSM5434420 c.1198G>A p.E400K Substitution - Missense 19:57129873-57129873 + TCGA-AX-A0J0-01 COSM1002090 c.2547G>T p.Q849H Substitution - Missense 19:57131222-57131222 + TCGA-EJ-5507-01 COSM1129695 c.665T>C p.L222S Substitution - Missense 19:57129340-57129340 + CSCC-31-T COSM4552353 c.556G>A p.E186K Substitution - Missense 19:57129231-57129231 + YUSCA COSM3540317 c.1909G>A p.D637N Substitution - Missense 19:57130584-57130584 + TCGA-AM-5820-01 COSM3757307 c.2055G>A p.V685V Substitution - coding silent 19:57130730-57130730 + T3064 COSM4739748 c.1385C>A p.T462K Substitution - Missense 19:57130060-57130060 + HCT116 COSM1681418 c.1309A>T p.I437F Substitution - Missense 19:57129984-57129984 + TCGA-AA-3672-01 COSM267733 c.196delA p.R68fs*7 Deletion - Frameshift 19:57128871-57128871 + TCGA-D5-6535-01 COSM1396948 c.1841G>T p.S614I Substitution - Missense 19:57130516-57130516 + TCGA-60-2721-01 COSM714266 c.576C>G p.N192K Substitution - Missense 19:57129251-57129251 + 8035732 COSM3389436 c.703A>T p.N235Y Substitution - Missense 19:57129378-57129378 + LUAD-S01302 COSM395738 c.627C>A p.N209K Substitution - Missense 19:57129302-57129302 + S01022 COSM5665878 c.2147A>G p.Y716C Substitution - Missense 19:57130822-57130822 + HN_62415 COSM130114 c.1751C>A p.T584N Substitution - Missense 19:57130426-57130426 + TCGA-AX-A0J0-01 COSM1002076 c.1023C>A p.F341L Substitution - Missense 19:57129698-57129698 + TCGA-FW-A3R5-06 COSM3893721 c.2556C>T p.A852A Substitution - coding silent 19:57131231-57131231 + HCC2998 COSM1681419 c.1355A>C p.N452T Substitution - Missense 19:57130030-57130030 + LUAD-YINHD COSM349676 c.1829G>T p.C610F Substitution - Missense 19:57130504-57130504 + LUAD-F00282 COSM367234 c.1699C>T p.Q567* Substitution - Nonsense 19:57130374-57130374 + 2492722 COSM3540286 c.154C>T p.Q52* Substitution - Nonsense 19:57128829-57128829 + TCGA-BR-8080-01 COSM4081974 c.1584A>G p.Q528Q Substitution - coding silent 19:57130259-57130259 + TCGA-AA-3492-01 COSM1396939 c.195_196insA p.R68fs*18 Insertion - Frameshift 19:57128870-57128871 + TCGA-DK-A2I4-01 COSM3797593 c.781G>C p.E261Q Substitution - Missense 19:57129456-57129456 + LP6005500-DNA_E03 COSM5034686 c.1606A>C p.S536R Substitution - Missense 19:57130281-57130281 + TCGA-B7-5818-01 COSM4081978 c.2708C>T p.T903I Substitution - Missense 19:57131383-57131383 + TCGA-19-2629-01 COSM3404699 c.1189A>G p.T397A Substitution - Missense 19:57129864-57129864 + 585272 COSM324217 c.1220C>G p.S407C Substitution - Missense 19:57129895-57129895 + TCGA-FW-A3R5-06 COSM3893715 c.1110G>A p.Q370Q Substitution - coding silent 19:57129785-57129785 + ESCC_129 COSM5641871 c.1702G>T p.E568* Substitution - Nonsense 19:57130377-57130377 + DU-145 COSM1681420 c.2572G>T p.D858Y Substitution - Missense 19:57131247-57131247 + TCGA-BS-A0UF-01 COSM1002072 c.595T>C p.S199P Substitution - Missense 19:57129270-57129270 + BD173T COSM5500262 c.2450G>C p.G817A Substitution - Missense 19:57131125-57131125 + YUKSI COSM5390918 c.382G>A p.E128K Substitution - Missense 19:57129057-57129057 + 134427 COSM324216 c.1065A>T p.K355N Substitution - Missense 19:57129740-57129740 + RK021_C01 COSM1631129 c.859T>G p.F287V Substitution - Missense 19:57129534-57129534 + TCGA-AX-A0J0-01 COSM1002081 c.1428C>A p.F476L Substitution - Missense 19:57130103-57130103 + PT35 COSM5914214 c.1648C>T p.P550S Substitution - Missense 19:57130323-57130323 + HT115 COSM2971689 c.834T>G p.S278S Substitution - coding silent 19:57129509-57129509 + TCGA-AG-3892-01 COSM258335 c.2750C>A p.S917Y Substitution - Missense 19:57131425-57131425 + ASHPC_0013_Pa_P COSM3787802 c.1588T>C p.Y530H Substitution - Missense 19:57130263-57130263 + SC_9066 COSM5571666 c.1774G>C p.V592L Substitution - Missense 19:57130449-57130449 + 256528 COSM3725113 c.678T>A p.P226P Substitution - coding silent 19:57129353-57129353 + TCGA-GV-A3JZ-01 COSM1305180 c.2734G>A p.E912K Substitution - Missense 19:57131409-57131409 + TCGA-13-2059-01 COSM1326135 c.804A>G p.R268R Substitution - coding silent 19:57129479-57129479 + PT21_2 COSM2971673 c.263C>T p.S88F Substitution - Missense 19:57128938-57128938 + TCGA-D9-A3Z4-01 COSM3540312 c.1396C>T p.P466S Substitution - Missense 19:57130071-57130071 + S02292 COSM5687686 c.120C>A p.V40V Substitution - coding silent 19:57128795-57128795 + ME029T COSM226834 c.2530G>A p.D844N Substitution - Missense 19:57131205-57131205 + CSCC-27-T COSM4452478 c.1908A>C p.R636S Substitution - Missense 19:57130583-57130583 + LUAD_E00522 COSM352772 c.2717G>T p.G906V Substitution - Missense 19:57131392-57131392 + TCGA-43-6143-01 COSM714262 c.1024T>C p.C342R Substitution - Missense 19:57129699-57129699 + TCGA-BR-8680-01 COSM4081971 c.1169A>C p.K390T Substitution - Missense 19:57129844-57129844 + ESCC_132 COSM5642390 c.1801G>A p.A601T Substitution - Missense 19:57130476-57130476 + PT38 COSM5923335 c.1684G>T p.V562F Substitution - Missense 19:57130359-57130359 + ESCC_130 COSM5642094 c.15G>A p.K5K Substitution - coding silent 19:57128690-57128690 + HCC1395 COSM27235 c.1362C>G p.L454L Substitution - coding silent 19:57130037-57130037 + NYU274 COSM4771380 c.2485G>T p.V829F Substitution - Missense 19:57131160-57131160 + TCGA-EE-A2GO-06 COSM1712973 c.2572G>A p.D858N Substitution - Missense 19:57131247-57131247 + TCGA-C4-A0EZ-01 COSM418003 c.1937C>T p.P646L Substitution - Missense 19:57130612-57130612 + TCGA-33-4566-01 COSM714258 c.2425G>T p.E809* Substitution - Nonsense 19:57131100-57131100 + Au1 COSM5597860 c.1018G>A p.D340N Substitution - Missense 19:57129693-57129693 + TCGA-60-2725-01 COSM714269 c.209G>T p.S70I Substitution - Missense 19:57128884-57128884 + TCGA-EW-A1PH-01 COSM1002077 c.1198G>T p.E400* Substitution - Nonsense 19:57129873-57129873 + TCGA-FR-A3YO-06 COSM3540296 c.642G>A p.E214E Substitution - coding silent 19:57129317-57129317 + 2334199 COSM324218 c.799C>A p.P267T Substitution - Missense 19:57129474-57129474 + TCGA-EE-A17X-06 COSM3540312 c.1396C>T p.P466S Substitution - Missense 19:57130071-57130071 + CSCC-32-T COSM4452455 c.1871A>T p.N624I Substitution - Missense 19:57130546-57130546 + YURISA COSM1396940 c.477G>A p.K159K Substitution - coding silent 19:57129152-57129152 + TCGA-D3-A1Q6-06 COSM3540308 c.1279A>G p.N427D Substitution - Missense 19:57129954-57129954 + TCGA-EE-A2M6-06 COSM2971673 c.263C>T p.S88F Substitution - Missense 19:57128938-57128938 + TCGA-FW-A3R5-06 COSM3893716 c.1164G>A p.M388I Substitution - Missense 19:57129839-57129839 + TCGA-CZ-5461-01 COSM475364 c.2498G>A p.G833E Substitution - Missense 19:57131173-57131173 + ACINAR03 COSM1002086 c.1921G>A p.G641S Substitution - Missense 19:57130596-57130596 + YURIF COSM1712968 c.833C>T p.S278F Substitution - Missense 19:57129508-57129508 + 2492721 COSM3540286 c.154C>T p.Q52* Substitution - Nonsense 19:57128829-57128829 + 37M COSM5584236 c.1702G>A p.E568K Substitution - Missense 19:57130377-57130377 + TCGA-BS-A0UV-01 COSM1002085 c.1920C>T p.I640I Substitution - coding silent 19:57130595-57130595 + TCGA-EE-A184-06 COSM3540319 c.2194G>T p.E732* Substitution - Nonsense 19:57130869-57130869 + TCGA-18-3406-01 COSM714263 c.871G>A p.G291R Substitution - Missense 19:57129546-57129546 + PD7215a COSM5788915 c.1076C>T p.S359L Substitution - Missense 19:57129751-57129751 + TCGA-FW-A3R5-06 COSM3893713 c.343G>A p.D115N Substitution - Missense 19:57129018-57129018 + TCGA-EE-A2A0-06 COSM3540301 c.920C>T p.P307L Substitution - Missense 19:57129595-57129595 + T1182 COSM4739747 c.1325G>A p.G442D Substitution - Missense 19:57130000-57130000 + YULOCUS COSM5390919 c.857G>A p.G286E Substitution - Missense 19:57129532-57129532 + TCGA-EE-A29D-06 COSM3540297 c.706C>T p.P236S Substitution - Missense 19:57129381-57129381 + YUDUTY COSM714272 c.31C>T p.Q11* Substitution - Nonsense 19:57128706-57128706 + 88 COSM5013528 c.2609A>C p.Q870P Substitution - Missense 19:57131284-57131284 + TCGA-66-2734-01 COSM714255 c.2705G>C p.S902T Substitution - Missense 19:57131380-57131380 + PT50 COSM5597859 c.2170C>T p.P724S Substitution - Missense 19:57130845-57130845 + TCGA-AG-3892-01 COSM288702 c.1716G>T p.E572D Substitution - Missense 19:57130391-57130391 + CHEWS031 COSM4581484 c.2535G>T p.V845V Substitution - coding silent 19:57131210-57131210 + TCGA-A2-A4S2-01 COSM3835917 c.860T>C p.F287S Substitution - Missense 19:57129535-57129535 + CSCC-30-T COSM1712973 c.2572G>A p.D858N Substitution - Missense 19:57131247-57131247 + BD190T COSM1002080 c.1423C>A p.L475I Substitution - Missense 19:57130098-57130098 + TCGA-D1-A103-01 COSM1002083 c.1864C>A p.L622M Substitution - Missense 19:57130539-57130539 + CHC1592T COSM4791355 c.205C>A p.Q69K Substitution - Missense 19:57128880-57128880 + TCGA-GF-A6C8-06 COSM3893714 c.1071C>T p.V357V Substitution - coding silent 19:57129746-57129746 + TCGA-EB-A553-01 COSM3540305 c.1041G>A p.K347K Substitution - coding silent 19:57129716-57129716 + HT115 COSM2971697 c.1313G>A p.C438Y Substitution - Missense 19:57129988-57129988 + TCGA-FS-A1ZK-06 COSM3540307 c.1205G>A p.G402E Substitution - Missense 19:57129880-57129880 + CSCC-55-T COSM4454431 c.486A>T p.L162F Substitution - Missense 19:57129161-57129161 + TCGA-24-1847-01 COSM1326134 c.971C>G p.P324R Substitution - Missense 19:57129646-57129646 + TCGA-60-2708-01 COSM714259 c.1857G>C p.Q619H Substitution - Missense 19:57130532-57130532 + TCGA-AA-A010-01 COSM286392 c.906G>A p.S302S Substitution - coding silent 19:57129581-57129581 + CSCC-29-T COSM4568341 c.1095T>A p.F365L Substitution - Missense 19:57129770-57129770 + TCGA-EE-A2GI-06 COSM3540323 c.2560T>C p.F854L Substitution - Missense 19:57131235-57131235 + UMC11 COSM2971675 c.295C>A p.L99M Substitution - Missense 19:57128970-57128970 + CSCC-56-T COSM4475013 c.1959C>T p.D653D Substitution - coding silent 19:57130634-57130634 + HCC042T COSM5823778 c.591A>T p.T197T Substitution - coding silent 19:57129266-57129266 + TCGA-A8-A08Z-01 COSM440460 c.211C>T p.H71Y Substitution - Missense 19:57128886-57128886 + CSCC-29-T COSM3540321 c.2455C>T p.P819S Substitution - Missense 19:57131130-57131130 + ESCC-250T COSM3540315 c.1743G>A p.M581I Substitution - Missense 19:57130418-57130418 + 112497 COSM95447 c.233A>C p.N78T Substitution - Missense 19:57128908-57128908 + TCGA-EE-A3AG-06 COSM3540310 c.1368C>T p.I456I Substitution - coding silent 19:57130043-57130043 + 2290929 COSM4440541 c.2368G>A p.D790N Substitution - Missense 19:57131043-57131043 + TCGA-EE-A2GI-06 COSM3540316 c.1765G>A p.D589N Substitution - Missense 19:57130440-57130440 + YUBER COSM1712973 c.2572G>A p.D858N Substitution - Missense 19:57131247-57131247 + TCGA-EE-A2MH-06 COSM3540286 c.154C>T p.Q52* Substitution - Nonsense 19:57128829-57128829 + T658 COSM375031 c.1909G>T p.D637Y Substitution - Missense 19:57130584-57130584 + 35M COSM5583010 c.1769C>T p.S590F Substitution - Missense 19:57130444-57130444 + PT32 COSM4563182 c.961G>A p.E321K Substitution - Missense 19:57129636-57129636 + 10 COSM87835 c.1658G>T p.S553I Substitution - Missense 19:57130333-57130333 + YUSIPU COSM5390920 c.1165G>A p.E389K Substitution - Missense 19:57129840-57129840 + TCGA-D3-A3C7-06 COSM3540283 c.53G>A p.G18E Substitution - Missense 19:57128728-57128728 + CH-60-T2 COSM1396939 c.195_196insA p.R68fs*18 Insertion - Frameshift 19:57128870-57128871 + 206T COSM1726892 c.2441T>C p.V814A Substitution - Missense 19:57131116-57131116 + RK187_C01 COSM3743165 c.1547T>C p.F516S Substitution - Missense 19:57130222-57130222 + TCGA-EB-A3Y7-01 COSM3540286 c.154C>T p.Q52* Substitution - Nonsense 19:57128829-57128829 + TCGA-EE-A3AC-06 COSM3540321 c.2455C>T p.P819S Substitution - Missense 19:57131130-57131130 + XHDG09 COSM4768562 c.385A>G p.I129V Substitution - Missense 19:57129060-57129060 + TCGA-AG-A002-01 COSM264602 c.1118C>T p.A373V Substitution - Missense 19:57129793-57129793 + TCGA-EE-A3AG-06 COSM286391 c.670C>T p.L224F Substitution - Missense 19:57129345-57129345 + TCGA-13-1484-01 COSM73228 c.831C>A p.D277E Substitution - Missense 19:57129506-57129506 + ESO-169 COSM1270072 c.1437A>C p.E479D Substitution - Missense 19:57130112-57130112 + NCI-H727 COSM2971731 c.2587G>T p.E863* Substitution - Nonsense 19:57131262-57131262 + CSCC-5-T COSM4566459 c.381_382GG>AA p.E128K Substitution - Missense 19:57129056-57129057 + 2492711 COSM5607193 c.1770C>T p.S590S Substitution - coding silent 19:57130445-57130445 + TCGA-D3-A5GN-06 COSM3540322 c.2496C>T p.I832I Substitution - coding silent 19:57131171-57131171 + 6T COSM3734614 c.2497G>A p.G833R Substitution - Missense 19:57131172-57131172 + TCGA-10-0931-01 COSM79092 c.2155A>T p.K719* Substitution - Nonsense 19:57130830-57130830 + TCGA-D5-6928-01 COSM267733 c.196delA p.R68fs*7 Deletion - Frameshift 19:57128871-57128871 + 587376 COSM1232019 c.1610T>G p.L537* Substitution - Nonsense 19:57130285-57130285 + TCGA-D3-A2JL-06 COSM3540302 c.948A>C p.Q316H Substitution - Missense 19:57129623-57129623 + TCGA-BF-A1Q0-01 COSM3540309 c.1352A>C p.N451T Substitution - Missense 19:57130027-57130027 + CSCC-27-T COSM3893717 c.1627G>A p.E543K Substitution - Missense 19:57130302-57130302 + PT48 COSM5933958 c.2173G>A p.E725K Substitution - Missense 19:57130848-57130848 + I-02 COSM4767223 c.1469A>T p.K490M Substitution - Missense 19:57130144-57130144 + 1_PRE-TREATMENT COSM1720946 c.863C>T p.P288L Substitution - Missense 19:57129538-57129538 + LUAD_E00565 COSM389326 c.1250C>A p.T417N Substitution - Missense 19:57129925-57129925 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.515632 19q13.43 609546

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.E479D c.1437A>C 19 57641480 ESCA A C Missense p.I797L c.2389A>C 19 57642432 BRCA A C Missense p.K390N c.1170A>C 19 57641213 LUAD A C Missense p.K490T c.1469A>C 19 57641512 LUSC A C Missense p.N451T c.1352A>C 19 57641395 CM A C Missense p.Q301P c.902A>C 19 57640945 HNSC A C Missense p.Q316H c.948A>C 19 57640991 CM A G IntronicSNV . c.1-6119A>G 19 57633925 CLL A G Missense p.K196E c.586A>G 19 57640629 LUAD A G Missense p.K201R c.602A>G 19 57640645 LUAD A G Missense p.K490E c.1468A>G 19 57641511 ESCA A G Missense p.K668E c.2002A>G 19 57642045 CM A G Missense p.N427D c.1279A>G 19 57641322 CM A G Missense p.S212G c.634A>G 19 57640677 STAD A G Missense p.T397A c.1189A>G 19 57641232 GBM A T Missense p.I2L c.4A>T 19 57640047 LUAD A T Missense p.K355N c.1065A>T 19 57641108 SCLC A T Missense p.Q284L c.851A>T 19 57640894 LUSC A T Nonsense p.K196* c.586A>T 19 57640629 LUAD A T Nonsense p.K719* c.2155A>T 19 57642198 OV A T Nonsense p.K778* c.2332A>T 19 57642375 MM A T Synonymous p.I48I c.144A>T 19 57640187 LUAD C A Missense p.A298E c.893C>A 19 57640936 SCLC C A Missense p.A373D c.1118C>A 19 57641161 LUAD C A Missense p.D277E c.831C>A 19 57640874 OV C A Missense p.F81L c.243C>A 19 57640286 UCEC C A Missense p.H688N c.2062C>A 19 57642105 HNSC C A Missense p.L126M c.376C>A 19 57640419 LUAD C A Missense p.L283M c.847C>A 19 57640890 LUAD C A Missense p.L38M c.112C>A 19 57640155 LUAD C A Missense p.L465I c.1393C>A 19 57641436 LUAD C A Missense p.L583M c.1747C>A 19 57641790 LUAD C A Missense p.N79K c.237C>A 19 57640280 LUAD C A Missense p.P210Q c.629C>A 19 57640672 LUAD C A Missense p.P267T c.799C>A 19 57640842 SCLC C A Missense p.Q334K c.1000C>A 19 57641043 HNSC C A Missense p.Q736K c.2206C>A 19 57642249 STAD C A Missense p.T584N c.1751C>A 19 57641794 HNSC C A Nonsense p.Y295* c.885C>A 19 57640928 LUAD C A Synonymous p.A822A c.2466C>A 19 57642509 LUAD C A Synonymous p.R899R c.2695C>A 19 57642738 RCCC C G Missense p.L549V c.1645C>G 19 57641688 LUAD C G Missense p.N192K c.576C>G 19 57640619 LUSC C G Missense p.S407C c.1220C>G 19 57641263 SCLC C T 3-UTRSNV . c.2766+170C>T 19 57642979 CM C T Missense p.H71Y c.211C>T 19 57640254 BRCA C T Missense p.L224F c.670C>T 19 57640713 CM C T Missense p.L328F c.982C>T 19 57641025 CM C T Missense p.P110S c.328C>T 19 57640371 BRCA C T Missense p.P307L c.920C>T 19 57640963 CM C T Missense p.P307S c.919C>T 19 57640962 CM C T Missense p.P319S c.955C>T 19 57640998 CM C T Missense p.P466S c.1396C>T 19 57641439 CM C T Missense p.P646L c.1937C>T 19 57641980 BLCA C T Missense p.P819S c.2455C>T 19 57642498 CM C T Missense p.S113F c.338C>T 19 57640381 CM C T Missense p.S153L c.458C>T 19 57640501 CM C T Missense p.S302L c.905C>T 19 57640948 CM C T Missense p.S308F c.923C>T 19 57640966 CM C T Missense p.S88F c.263C>T 19 57640306 CM C T Missense p.T230I c.689C>T 19 57640732 CM C T Missense p.T903I c.2708C>T 19 57642751 STAD C T Nonsense p.Q11* c.31C>T 19 57640074 LUSC C T Nonsense p.Q52* c.154C>T 19 57640197 CM C T Nonsense p.Q777* c.2329C>T 19 57642372 CM C T Synonymous p.H459H c.1377C>T 19 57641420 LUAD C T Synonymous p.I456I c.1368C>T 19 57641411 CM C T Synonymous p.I908I c.2724C>T 19 57642767 CM C T Synonymous p.L248L c.744C>T 19 57640787 CM C T Synonymous p.L26L c.78C>T 19 57640121 CM C T Synonymous p.N231N c.693C>T 19 57640736 MM C T Synonymous p.P110P c.330C>T 19 57640373 CM C T Synonymous p.P594P c.1782C>T 19 57641825 STAD C T Synonymous p.S515S c.1545C>T 19 57641588 CM C T Synonymous p.S711S c.2133C>T 19 57642176 CM C T Synonymous p.V633V c.1899C>T 19 57641942 CM C T Synonymous p.V829V c.2487C>T 19 57642530 CM C T Synonymous p.Y823Y c.2469C>T 19 57642512 UCEC C T Synonymous p.Y841Y c.2523C>T 19 57642566 CM G A Missense p.A627T c.1879G>A 19 57641922 COREAD G A Missense p.D116N c.346G>A 19 57640389 CM G A Missense p.D176N c.526G>A 19 57640569 CM G A Missense p.D277N c.829G>A 19 57640872 BLCA G A Missense p.D589N c.1765G>A 19 57641808 CM G A Missense p.D637N c.1909G>A 19 57641952 CM G A Missense p.D649N c.1945G>A 19 57641988 HNSC G A Missense p.D844N c.2530G>A 19 57642573 CM G A Missense p.D858N c.2572G>A 19 57642615 CM G A Missense p.E259K c.775G>A 19 57640818 UCEC G A Missense p.E349K c.1045G>A 19 57641088 BLCA G A Missense p.E389K c.1165G>A 19 57641208 CM G A Missense p.E404K c.1210G>A 19 57641253 BLCA G A Missense p.E479K c.1435G>A 19 57641478 CM G A Missense p.E623K c.1867G>A 19 57641910 CM G A Missense p.E773K c.2317G>A 19 57642360 HNSC G A Missense p.E912K c.2734G>A 19 57642777 BLCA G A Missense p.G166S c.496G>A 19 57640539 CM G A Missense p.G18E c.53G>A 19 57640096 CM G A Missense p.G253S c.757G>A 19 57640800 CM G A Missense p.G291E c.872G>A 19 57640915 CM G A Missense p.G291R c.871G>A 19 57640914 LUSC G A Missense p.G402E c.1205G>A 19 57641248 CM G A Missense p.G45E c.134G>A 19 57640177 CM G A Missense p.G833E c.2498G>A 19 57642541 RCCC G A Missense p.G886R c.2656G>A 19 57642699 CM G A Missense p.M111I c.333G>A 19 57640376 CM G A Missense p.M581I c.1743G>A 19 57641786 CM G A Missense p.S14N c.41G>A 19 57640084 LUSC G A Missense p.V633I c.1897G>A 19 57641940 UCEC G A Nonsense p.W320* c.959G>A 19 57641002 CM G A Synonymous p.G398G c.1194G>A 19 57641237 CM G A Synonymous p.G886G c.2658G>A 19 57642701 CM G A Synonymous p.G911G c.2733G>A 19 57642776 CM G A Synonymous p.L126L c.378G>A 19 57640421 CM G A Synonymous p.L22L c.66G>A 19 57640109 CM G A Synonymous p.R497R c.1491G>A 19 57641534 COREAD G C Missense p.E217Q c.649G>C 19 57640692 LUSC G C Missense p.E261Q c.781G>C 19 57640824 BLCA G C Missense p.E702Q c.2104G>C 19 57642147 HNSC G C Missense p.M19I c.57G>C 19 57640100 LUSC G C Missense p.Q619H c.1857G>C 19 57641900 LUSC G C Missense p.R220T c.659G>C 19 57640702 CM G C Missense p.S902T c.2705G>C 19 57642748 LUSC GG TT Missense p.G558L c.1672_1673delinsTT 19 57641715 CM G T Missense p.G788C c.2362G>T 19 57642405 HNSC G T Missense p.K16N c.48G>T 19 57640091 HNSC G T Missense p.Q904H c.2712G>T 19 57642755 LUSC G T Missense p.R899L c.2696G>T 19 57642739 RCCC G T Missense p.S553I c.1658G>T 19 57641701 HNSC G T Missense p.S70I c.209G>T 19 57640252 LUSC G T Missense p.V177L c.529G>T 19 57640572 LUSC G T Missense p.V424F c.1270G>T 19 57641313 LUSC G T Nonsense p.E128* c.382G>T 19 57640425 LUSC G T Nonsense p.E259* c.775G>T 19 57640818 RCCC G T Nonsense p.E400* c.1198G>T 19 57641241 BRCA G T Nonsense p.E596* c.1786G>T 19 57641829 HNSC G T Nonsense p.E725* c.2173G>T 19 57642216 MM G T Nonsense p.E732* c.2194G>T 19 57642237 CM G T Synonymous p.G817G c.2451G>T 19 57642494 HNSC G T Synonymous p.L184L c.552G>T 19 57640595 LUAD T A Missense p.L350I c.1048T>A 19 57641091 CM T A Missense p.S571T c.1711T>A 19 57641754 GBM T A Missense p.S865T c.2593T>A 19 57642636 LUAD T C Missense p.C342R c.1024T>C 19 57641067 LUSC T C Missense p.F51L c.151T>C 19 57640194 CM T C Missense p.F854L c.2560T>C 19 57642603 CM T C Missense p.L222S c.665T>C 19 57640708 PRAD T C Synonymous p.D116D c.348T>C 19 57640391 CM T C Synonymous p.P901P c.2703T>C 19 57642746 RCCC T C Synonymous p.S553S c.1659T>C 19 57641702 COREAD T C Synonymous p.T132T c.396T>C 19 57640439 ESCA T G Missense p.C380G c.1138T>G 19 57641181 CM T G Missense p.D844E c.2532T>G 19 57642575 LUAD