Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 6 31615616 31615617 + Frame_Shift_Del DEL GA GA - TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr6:31615616_31615617delGA c.557_558delTC c.(556-558)ctcfs p.L186fs BLCA 6 31607379 31607379 + Silent SNP C C G TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr6:31607379C>G c.3201G>C c.(3199-3201)gtG>gtC p.V1067V BLCA 6 31608053 31608053 + Nonsense_Mutation SNP G G A TCGA-4Z-AA89-01A-11D-A391-08 TCGA-4Z-AA89-10A-01D-A394-08 g.chr6:31608053G>A c.3079C>T c.(3079-3081)Cag>Tag p.Q1027* BLCA 6 31609349 31609349 + Silent SNP G G A TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr6:31609349G>A c.2436C>T c.(2434-2436)atC>atT p.I812I BLCA 6 31612317 31612317 + Missense_Mutation SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr6:31612317G>A c.1450C>T c.(1450-1452)Cat>Tat p.H484Y BLCA 6 31615465 31615465 + Missense_Mutation SNP C C G TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr6:31615465C>G c.709G>C c.(709-711)Gaa>Caa p.E237Q BLCA 6 31617000 31617000 + Silent SNP G G A TCGA-DK-A1AB-01A-11D-A13W-08 TCGA-DK-A1AB-10A-01D-A13W-08 g.chr6:31617000G>A c.399C>T c.(397-399)gtC>gtT p.V133V BRCA 6 31608186 31608186 + Silent SNP T T C TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr6:31608186T>C c.3024A>G c.(3022-3024)gaA>gaG p.E1008E BRCA 6 31609988 31609989 + Frame_Shift_Ins INS - - A TCGA-BH-A0B1-01A-12W-A071-09 TCGA-BH-A0B1-10A-01W-A071-09 g.chr6:31609988_31609989insA c.2145_2146insT c.(2143-2148)tccctgfs p.L716fs BRCA 6 31611965 31611965 + Missense_Mutation SNP T T C TCGA-D8-A27F-01A-11D-A16D-09 TCGA-D8-A27F-10A-01D-A16D-09 g.chr6:31611965T>C c.1472A>G c.(1471-1473)cAg>cGg p.Q491R CESC 6 31607000 31607000 + Missense_Mutation SNP G G A TCGA-EK-A2RA-01A-11D-A18J-09 TCGA-EK-A2RA-10A-01D-A18J-09 g.chr6:31607000G>A c.3307C>T c.(3307-3309)Cgg>Tgg p.R1103W CESC 6 31610002 31610002 + Missense_Mutation SNP G G A TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr6:31610002G>A c.2132C>T c.(2131-2133)tCc>tTc p.S711F COAD 6 31608463 31608463 + Missense_Mutation SNP T T C TCGA-D5-6926-01A-11D-1924-10 TCGA-D5-6926-10A-01D-1924-10 g.chr6:31608463T>C c.2863A>G c.(2863-2865)Atg>Gtg p.M955V COAD 6 31608571 31608571 + Frame_Shift_Del DEL G G - TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:31608571delG c.2842delC c.(2842-2844)cagfs p.Q948fs COAD 6 31608571 31608571 + Frame_Shift_Del DEL G G - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr6:31608571delG c.2842delC c.(2842-2844)cagfs p.Q948fs COAD 6 31608918 31608918 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:31608918T>C c.2660A>G c.(2659-2661)cAg>cGg p.Q887R COAD 6 31610163 31610163 + Silent SNP A A G TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr6:31610163A>G c.1971T>C c.(1969-1971)ccT>ccC p.P657P COAD 6 31610801 31610801 + Silent SNP G G T TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr6:31610801G>T c.1758C>A c.(1756-1758)ccC>ccA p.P586P COAD 6 31612849 31612849 + Missense_Mutation SNP C C T TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr6:31612849C>T c.1261G>A c.(1261-1263)Gag>Aag p.E421K COAD 6 31612922 31612923 + Frame_Shift_Ins INS - - G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr6:31612922_31612923insG c.1187_1188insC c.(1186-1188)ccafs p.P396fs COAD 6 31615400 31615400 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr6:31615400G>A c.774C>T c.(772-774)ggC>ggT p.G258G COAD 6 31619438 31619438 + Frame_Shift_Del DEL C C - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr6:31619438delC c.103delG c.(103-105)gccfs p.A35fs COADREAD 6 31608463 31608463 + Missense_Mutation SNP T T C TCGA-D5-6926-01A-11D-1924-10 TCGA-D5-6926-10A-01D-1924-10 g.chr6:31608463T>C c.2863A>G c.(2863-2865)Atg>Gtg p.M955V COADREAD 6 31608571 31608571 + Frame_Shift_Del DEL G G - TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:31608571delG c.2842delC c.(2842-2844)cagfs p.Q948fs COADREAD 6 31608571 31608571 + Frame_Shift_Del DEL G G - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr6:31608571delG c.2842delC c.(2842-2844)cagfs p.Q948fs COADREAD 6 31608918 31608918 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr6:31608918T>C c.2660A>G c.(2659-2661)cAg>cGg p.Q887R COADREAD 6 31609993 31609993 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:31609993C>T c.2141G>A c.(2140-2142)gGc>gAc p.G714D COADREAD 6 31610163 31610163 + Silent SNP A A G TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr6:31610163A>G c.1971T>C c.(1969-1971)ccT>ccC p.P657P COADREAD 6 31610801 31610801 + Silent SNP G G T TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr6:31610801G>T c.1758C>A c.(1756-1758)ccC>ccA p.P586P COADREAD 6 31612849 31612849 + Missense_Mutation SNP C C T TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr6:31612849C>T c.1261G>A c.(1261-1263)Gag>Aag p.E421K COADREAD 6 31612922 31612923 + Frame_Shift_Ins INS - - G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr6:31612922_31612923insG c.1187_1188insC c.(1186-1188)ccafs p.P396fs COADREAD 6 31615400 31615400 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr6:31615400G>A c.774C>T c.(772-774)ggC>ggT p.G258G COADREAD 6 31619438 31619438 + Frame_Shift_Del DEL C C - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr6:31619438delC c.103delG c.(103-105)gccfs p.A35fs ESCA 6 31610093 31610093 + Missense_Mutation SNP G G C TCGA-IG-A625-01A-11D-A31U-09 TCGA-IG-A625-10A-01D-A31U-09 g.chr6:31610093G>C c.2041C>G c.(2041-2043)Cct>Gct p.P681A ESCA 6 31615559 31615559 + Silent SNP C C T TCGA-Z6-AAPN-01A-11D-A403-09 TCGA-Z6-AAPN-10A-01D-A403-09 g.chr6:31615559C>T c.615G>A c.(613-615)caG>caA p.Q205Q ESCA 6 31617094 31617094 + Missense_Mutation SNP G G T TCGA-R6-A8W8-01B-11D-A37C-09 TCGA-R6-A8W8-10A-01D-A37F-09 g.chr6:31617094G>T c.305C>A c.(304-306)aCg>aAg p.T102K GBMLGG 6 31611887 31611887 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:31611887G>T c.1550C>A c.(1549-1551)cCt>cAt p.P517H GBMLGG 6 31612853 31612853 + Missense_Mutation SNP A A C TCGA-FG-7637-01A-11D-2086-08 TCGA-FG-7637-10A-01D-2086-08 g.chr6:31612853A>C c.1257T>G c.(1255-1257)aaT>aaG p.N419K GBMLGG 6 31612931 31612931 + Silent SNP C C G TCGA-HT-7689-01A-11D-2253-08 TCGA-HT-7689-10A-01D-2253-08 g.chr6:31612931C>G c.1179G>C c.(1177-1179)cgG>cgC p.R393R HNSC 6 31606973 31606973 + Missense_Mutation SNP C C T TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr6:31606973C>T c.3334G>A c.(3334-3336)Gaa>Aaa p.E1112K HNSC 6 31609355 31609355 + Silent SNP T T C TCGA-CV-A6K0-01B-21D-A31L-08 TCGA-CV-A6K0-10A-01D-A31J-08 g.chr6:31609355T>C c.2430A>G c.(2428-2430)acA>acG p.T810T HNSC 6 31610753 31610754 + Frame_Shift_Ins INS - - A TCGA-BA-6870-01A-11D-1870-08 TCGA-BA-6870-10A-01D-1870-08 g.chr6:31610753_31610754insA c.1805_1806insT c.(1804-1806)atgfs p.M602fs HNSC 6 31612823 31612823 + Silent SNP C C T TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr6:31612823C>T c.1287G>A c.(1285-1287)ccG>ccA p.P429P KIPAN 6 31609641 31609642 + Frame_Shift_Ins INS - - G TCGA-CJ-4904-01A-02D-1429-08 TCGA-CJ-4904-11A-01D-1429-08 g.chr6:31609641_31609642insG c.2326_2327insC c.(2326-2328)cagfs p.Q776fs KIPAN 6 31611899 31611899 + Missense_Mutation SNP C C A TCGA-CJ-4918-01A-01D-1429-08 TCGA-CJ-4918-11A-01D-1429-08 g.chr6:31611899C>A c.1538G>T c.(1537-1539)cGg>cTg p.R513L KIPAN 6 31615405 31615405 + Missense_Mutation SNP C C T TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr6:31615405C>T c.769G>A c.(769-771)Gcg>Acg p.A257T KIRC 6 31609641 31609642 + Frame_Shift_Ins INS - - G TCGA-CJ-4904-01A-02D-1429-08 TCGA-CJ-4904-11A-01D-1429-08 g.chr6:31609641_31609642insG c.2326_2327insC c.(2326-2328)cagfs p.Q776fs KIRC 6 31611899 31611899 + Missense_Mutation SNP C C A TCGA-CJ-4918-01A-01D-1429-08 TCGA-CJ-4918-11A-01D-1429-08 g.chr6:31611899C>A c.1538G>T c.(1537-1539)cGg>cTg p.R513L KIRC 6 31615405 31615405 + Missense_Mutation SNP C C T TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr6:31615405C>T c.769G>A c.(769-771)Gcg>Acg p.A257T LGG 6 31611887 31611887 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:31611887G>T c.1550C>A c.(1549-1551)cCt>cAt p.P517H LGG 6 31612853 31612853 + Missense_Mutation SNP A A C TCGA-FG-7637-01A-11D-2086-08 TCGA-FG-7637-10A-01D-2086-08 g.chr6:31612853A>C c.1257T>G c.(1255-1257)aaT>aaG p.N419K LGG 6 31612931 31612931 + Silent SNP C C G TCGA-HT-7689-01A-11D-2253-08 TCGA-HT-7689-10A-01D-2253-08 g.chr6:31612931C>G c.1179G>C c.(1177-1179)cgG>cgC p.R393R LIHC 6 31608213 31608213 + Silent SNP T T C TCGA-CC-A7IJ-01A-11D-A33Q-10 TCGA-CC-A7IJ-10A-01D-A33Q-10 g.chr6:31608213T>C c.2997A>G c.(2995-2997)gaA>gaG p.E999E LIHC 6 31608658 31608658 + Missense_Mutation SNP C C T TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr6:31608658C>T c.2755G>A c.(2755-2757)Gga>Aga p.G919R LIHC 6 31610072 31610072 + Missense_Mutation SNP G G A TCGA-CC-A3MB-01A-11D-A20W-10 TCGA-CC-A3MB-10A-01D-A20W-10 g.chr6:31610072G>A c.2062C>T c.(2062-2064)Cct>Tct p.P688S LIHC 6 31610883 31610883 + Missense_Mutation SNP G G A TCGA-DD-A4NB-01A-12D-A25V-10 TCGA-DD-A4NB-11A-11D-A25V-10 g.chr6:31610883G>A c.1676C>T c.(1675-1677)aCc>aTc p.T559I LUAD 6 31608003 31608003 + Silent SNP G G A TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr6:31608003G>A c.3129C>T c.(3127-3129)ctC>ctT p.L1043L LUAD 6 31608189 31608189 + Silent SNP T T C TCGA-49-6761-01A-31D-1945-08 TCGA-49-6761-11A-01D-1945-08 g.chr6:31608189T>C c.3021A>G c.(3019-3021)acA>acG p.T1007T LUAD 6 31609167 31609167 + Silent SNP G G A TCGA-80-5607-01A-31D-1945-08 TCGA-80-5607-10A-01D-1946-08 g.chr6:31609167G>A c.2502C>T c.(2500-2502)atC>atT p.I834I LUAD 6 31610072 31610072 + Missense_Mutation SNP G G C TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr6:31610072G>C c.2062C>G c.(2062-2064)Cct>Gct p.P688A LUAD 6 31612330 31612330 + Silent SNP C C T TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr6:31612330C>T c.1437G>A c.(1435-1437)ctG>ctA p.L479L LUAD 6 31612763 31612763 + Silent SNP C C T TCGA-44-2657-01A-01D-1105-08 TCGA-44-2657-10A-01D-1105-08 g.chr6:31612763C>T c.1347G>A c.(1345-1347)caG>caA p.Q449Q LUAD 6 31612875 31612875 + Missense_Mutation SNP G G C TCGA-38-4628-01A-01D-1265-08 TCGA-38-4628-11A-01D-1265-08 g.chr6:31612875G>C c.1235C>G c.(1234-1236)tCc>tGc p.S412C LUAD 6 31614237 31614237 + Silent SNP G G C TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr6:31614237G>C c.870C>G c.(868-870)ctC>ctG p.L290L LUAD 6 31615436 31615436 + Missense_Mutation SNP C C G TCGA-55-8510-01A-11D-2393-08 TCGA-55-8510-10A-01D-2393-08 g.chr6:31615436C>G c.738G>C c.(736-738)caG>caC p.Q246H LUAD 6 31616977 31616977 + Splice_Site SNP G G T TCGA-49-6767-01A-11D-1855-08 TCGA-49-6767-11A-01D-1855-08 g.chr6:31616977G>T c.422C>A c.(421-423)cCt>cAt p.P141H LUAD 6 31617043 31617043 + Missense_Mutation SNP C C A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr6:31617043C>A c.356G>T c.(355-357)gGg>gTg p.G119V LUSC 6 31607333 31607333 + Missense_Mutation SNP C C T TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr6:31607333C>T c.3247G>A c.(3247-3249)Gag>Aag p.E1083K LUSC 6 31608925 31608925 + Missense_Mutation SNP C C A TCGA-39-5016-01A-01D-1441-08 TCGA-39-5016-11A-01D-1441-08 g.chr6:31608925C>A c.2653G>T c.(2653-2655)Ggg>Tgg p.G885W LUSC 6 31609651 31609651 + Missense_Mutation SNP C C A TCGA-66-2780-01A-01D-1522-08 TCGA-66-2780-11A-01D-1522-08 g.chr6:31609651C>A c.2317G>T c.(2317-2319)Ggg>Tgg p.G773W OV 6 31614186 31614186 + Silent SNP C C T TCGA-25-1633-01A-01W-0615-10 TCGA-25-1633-10A-01W-0616-10 g.chr6:31614186C>T c.921G>A c.(919-921)acG>acA p.T307T PAAD 6 31609612 31609612 + Nonsense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:31609612G>A c.2356C>T c.(2356-2358)Cga>Tga p.R786* PAAD 6 31617055 31617055 + Frame_Shift_Del DEL G G - TCGA-3A-A9IX-01A-11D-A40W-08 TCGA-3A-A9IX-10A-01D-A40W-08 g.chr6:31617055delG c.344delC c.(343-345)cctfs p.P115fs PRAD 6 31608180 31608180 + Nonsense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:31608180C>T c.3030G>A c.(3028-3030)tgG>tgA p.W1010* PRAD 6 31608917 31608917 + Missense_Mutation SNP C C A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:31608917C>A c.2661G>T c.(2659-2661)caG>caT p.Q887H PRAD 6 31614196 31614196 + Missense_Mutation SNP G G A TCGA-HC-7752-01A-11D-2114-08 TCGA-HC-7752-10A-01D-2115-08 g.chr6:31614196G>A c.911C>T c.(910-912)gCt>gTt p.A304V PRAD 6 31614220 31614220 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:31614220C>T c.887G>A c.(886-888)cGc>cAc p.R296H PRAD 6 31614295 31614295 + Missense_Mutation SNP G G T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:31614295G>T c.812C>A c.(811-813)cCt>cAt p.P271H READ 6 31609993 31609993 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr6:31609993C>T c.2141G>A c.(2140-2142)gGc>gAc p.G714D SARC 6 31613261 31613261 + Nonsense_Mutation SNP G G A TCGA-JV-A5VF-01A-11D-A29N-09 TCGA-JV-A5VF-10A-01D-A29N-09 g.chr6:31613261G>A c.1057C>T c.(1057-1059)Cga>Tga p.R353* SKCM 6 31607321 31607321 + Missense_Mutation SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr6:31607321G>A c.3259C>T c.(3259-3261)Cgg>Tgg p.R1087W SKCM 6 31607322 31607322 + Silent SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr6:31607322G>A c.3258C>T c.(3256-3258)agC>agT p.S1086S SKCM 6 31608000 31608000 + Silent SNP A A G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr6:31608000A>G c.3132T>C c.(3130-3132)agT>agC p.S1044S SKCM 6 31608042 31608042 + Silent SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr6:31608042C>T c.3090G>A c.(3088-3090)cgG>cgA p.R1030R SKCM 6 31608608 31608608 + Silent SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr6:31608608G>A c.2805C>T c.(2803-2805)gcC>gcT p.A935A SKCM 6 31609612 31609612 + Nonsense_Mutation SNP G G A TCGA-EE-A2GE-06A-11D-A196-08 TCGA-EE-A2GE-10A-01D-A198-08 g.chr6:31609612G>A c.2356C>T c.(2356-2358)Cga>Tga p.R786* SKCM 6 31609699 31609699 + Missense_Mutation SNP G G A TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr6:31609699G>A c.2269C>T c.(2269-2271)Ctt>Ttt p.L757F SKCM 6 31610092 31610092 + Missense_Mutation SNP G G A TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr6:31610092G>A c.2042C>T c.(2041-2043)cCt>cTt p.P681L SKCM 6 31610669 31610669 + Silent SNP G G C TCGA-ER-A19J-06A-11D-A196-08 TCGA-ER-A19J-10A-01D-A198-08 g.chr6:31610669G>C c.1890C>G c.(1888-1890)ccC>ccG p.P630P SKCM 6 31611729 31611729 + Missense_Mutation SNP G G T TCGA-DA-A1I4-06A-11D-A196-08 TCGA-DA-A1I4-10A-01D-A198-08 g.chr6:31611729G>T c.1604C>A c.(1603-1605)gCc>gAc p.A535D SKCM 6 31611951 31611951 + Missense_Mutation SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr6:31611951G>A c.1486C>T c.(1486-1488)Cca>Tca p.P496S SKCM 6 31612752 31612752 + Missense_Mutation SNP G G A TCGA-ER-A19H-06A-12D-A196-08 TCGA-ER-A19H-10A-01D-A198-08 g.chr6:31612752G>A c.1358C>T c.(1357-1359)cCc>cTc p.P453L SKCM 6 31612874 31612874 + Silent SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr6:31612874G>A c.1236C>T c.(1234-1236)tcC>tcT p.S412S SKCM 6 31612884 31612884 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr6:31612884T>C c.1226A>G c.(1225-1227)cAg>cGg p.Q409R SKCM 6 31613319 31613319 + Silent SNP C C A TCGA-EE-A183-06A-11D-A196-08 TCGA-EE-A183-10A-01D-A198-08 g.chr6:31613319C>A c.999G>T c.(997-999)ctG>ctT p.L333L SKCM 6 31614291 31614291 + Silent SNP G G A TCGA-GN-A4U7-06A-21D-A32N-08 TCGA-GN-A4U7-10B-01D-A32N-08 g.chr6:31614291G>A c.816C>T c.(814-816)tcC>tcT p.S272S SKCM 6 31615554 31615554 + Missense_Mutation SNP G G A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr6:31615554G>A c.620C>T c.(619-621)cCg>cTg p.P207L SKCM 6 31615563 31615563 + Missense_Mutation SNP G G A TCGA-DA-A1I5-06A-11D-A197-08 TCGA-DA-A1I5-10A-01D-A199-08 g.chr6:31615563G>A c.611C>T c.(610-612)cCg>cTg p.P204L SKCM 6 31617056 31617056 + Missense_Mutation SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr6:31617056G>A c.343C>T c.(343-345)Cct>Tct p.P115S SKCM 6 31617103 31617103 + Missense_Mutation SNP G G T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr6:31617103G>T c.296C>A c.(295-297)tCt>tAt p.S99Y

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 6 31604113 31604113 single base substitution G A downstream_gene_variant BLCA-CN 6 31609320 31609320 single base substitution C T downstream_gene_variant BLCA-CN 6 31609320 31609320 single base substitution C T exon_variant BLCA-CN 6 31609320 31609320 single base substitution C T missense_variant S690N 2069G>A BLCA-CN 6 31609320 31609320 single base substitution C T missense_variant S816N 2447G>A BLCA-CN 6 31609320 31609320 single base substitution C T missense_variant S822N 2465G>A BLCA-CN 6 31609320 31609320 single base substitution C T missense_variant S852N 2555G>A BLCA-CN 6 31609320 31609320 single base substitution C T upstream_gene_variant BLCA-US 6 31602048 31602062 deletion of <=200bp GGGCTCTAAGCCTGA - downstream_gene_variant BLCA-US 6 31602332 31602332 single base substitution G C downstream_gene_variant BLCA-US 6 31609349 31609349 single base substitution G A downstream_gene_variant BLCA-US 6 31609349 31609349 single base substitution G A exon_variant BLCA-US 6 31609349 31609349 single base substitution G A synonymous_variant I680I 2040C>T BLCA-US 6 31609349 31609349 single base substitution G A synonymous_variant I806I 2418C>T BLCA-US 6 31609349 31609349 single base substitution G A synonymous_variant I812I 2436C>T BLCA-US 6 31609349 31609349 single base substitution G A synonymous_variant I842I 2526C>T BLCA-US 6 31609349 31609349 single base substitution G A upstream_gene_variant BLCA-US 6 31617000 31617000 single base substitution G A synonymous_variant V133V 399C>T BLCA-US 6 31617000 31617000 single base substitution G A upstream_gene_variant BLCA-US 6 31625244 31625244 single base substitution T G upstream_gene_variant BOCA-FR 6 31611777 31611777 single base substitution T C downstream_gene_variant BOCA-FR 6 31611777 31611777 single base substitution T C intron_variant BOCA-FR 6 31611777 31611777 single base substitution T C upstream_gene_variant BRCA-EU 6 31601976 31601976 single base substitution C G downstream_gene_variant BRCA-EU 6 31603642 31603642 single base substitution A C downstream_gene_variant BRCA-EU 6 31603836 31603836 deletion of <=200bp G - downstream_gene_variant BRCA-EU 6 31604845 31604845 single base substitution C A downstream_gene_variant BRCA-EU 6 31605633 31605633 single base substitution T C downstream_gene_variant BRCA-EU 6 31605680 31605680 single base substitution G A downstream_gene_variant BRCA-EU 6 31606872 31606872 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 31606872 31606872 single base substitution C T downstream_gene_variant BRCA-EU 6 31606872 31606872 single base substitution C T exon_variant BRCA-EU 6 31608602 31608602 single base substitution G T downstream_gene_variant BRCA-EU 6 31608602 31608602 single base substitution G T exon_variant BRCA-EU 6 31608602 31608602 single base substitution G T synonymous_variant L37L 111C>A BRCA-EU 6 31608602 31608602 single base substitution G T synonymous_variant L79L 237C>A BRCA-EU 6 31608602 31608602 single base substitution G T synonymous_variant L805L 2415C>A BRCA-EU 6 31608602 31608602 single base substitution G T synonymous_variant L931L 2793C>A BRCA-EU 6 31608602 31608602 single base substitution G T synonymous_variant L937L 2811C>A BRCA-EU 6 31608602 31608602 single base substitution G T synonymous_variant L967L 2901C>A BRCA-EU 6 31608602 31608602 single base substitution G T upstream_gene_variant BRCA-EU 6 31609362 31609362 single base substitution G C downstream_gene_variant BRCA-EU 6 31609362 31609362 single base substitution G C exon_variant BRCA-EU 6 31609362 31609362 single base substitution G C missense_variant T676S 2027C>G BRCA-EU 6 31609362 31609362 single base substitution G C missense_variant T802S 2405C>G BRCA-EU 6 31609362 31609362 single base substitution G C missense_variant T808S 2423C>G BRCA-EU 6 31609362 31609362 single base substitution G C missense_variant T838S 2513C>G BRCA-EU 6 31609362 31609362 single base substitution G C upstream_gene_variant BRCA-EU 6 31612380 31612380 single base substitution C G downstream_gene_variant BRCA-EU 6 31612380 31612380 single base substitution C G intron_variant BRCA-EU 6 31612380 31612380 single base substitution C G missense_variant D51H 151G>C BRCA-EU 6 31612380 31612380 single base substitution C G splice_acceptor_variant BRCA-EU 6 31612380 31612380 single base substitution C G upstream_gene_variant BRCA-EU 6 31612923 31612923 insertion of <=200bp - G downstream_gene_variant BRCA-EU 6 31612923 31612923 insertion of <=200bp - G exon_variant BRCA-EU 6 31612923 31612923 insertion of <=200bp - G frameshift_variant P390P? BRCA-EU 6 31612923 31612923 insertion of <=200bp - G frameshift_variant P396P? BRCA-EU 6 31612923 31612923 insertion of <=200bp - G frameshift_variant P50P? BRCA-EU 6 31612923 31612923 insertion of <=200bp - G upstream_gene_variant BRCA-EU 6 31612931 31612931 single base substitution C G downstream_gene_variant BRCA-EU 6 31612931 31612931 single base substitution C G exon_variant BRCA-EU 6 31612931 31612931 single base substitution C G synonymous_variant R387R 1161G>C BRCA-EU 6 31612931 31612931 single base substitution C G synonymous_variant R393R 1179G>C BRCA-EU 6 31612931 31612931 single base substitution C G synonymous_variant R47R 141G>C BRCA-EU 6 31612931 31612931 single base substitution C G upstream_gene_variant BRCA-EU 6 31613048 31613048 single base substitution C G downstream_gene_variant BRCA-EU 6 31613048 31613048 single base substitution C G intron_variant BRCA-EU 6 31613048 31613048 single base substitution C G upstream_gene_variant BRCA-EU 6 31613058 31613058 single base substitution T C downstream_gene_variant BRCA-EU 6 31613058 31613058 single base substitution T C intron_variant BRCA-EU 6 31613058 31613058 single base substitution T C upstream_gene_variant BRCA-EU 6 31613378 31613378 single base substitution C A downstream_gene_variant BRCA-EU 6 31613378 31613378 single base substitution C A stop_gained E308* 922G>T BRCA-EU 6 31613378 31613378 single base substitution C A stop_gained E314* 940G>T BRCA-EU 6 31613378 31613378 single base substitution C A upstream_gene_variant BRCA-EU 6 31613421 31613421 single base substitution C G downstream_gene_variant BRCA-EU 6 31613421 31613421 single base substitution C G intron_variant BRCA-EU 6 31613421 31613421 single base substitution C G upstream_gene_variant BRCA-EU 6 31613724 31613724 single base substitution A G downstream_gene_variant BRCA-EU 6 31613724 31613724 single base substitution A G intron_variant BRCA-EU 6 31613724 31613724 single base substitution A G upstream_gene_variant BRCA-EU 6 31614955 31614955 single base substitution C T downstream_gene_variant BRCA-EU 6 31614955 31614955 single base substitution C T intron_variant BRCA-EU 6 31614955 31614955 single base substitution C T upstream_gene_variant BRCA-EU 6 31615600 31615600 single base substitution G C downstream_gene_variant BRCA-EU 6 31615600 31615600 single base substitution G C missense_variant R168G 502C>G BRCA-EU 6 31615600 31615600 single base substitution G C missense_variant R186G 556C>G BRCA-EU 6 31615600 31615600 single base substitution G C missense_variant R192G 574C>G BRCA-EU 6 31615600 31615600 single base substitution G C upstream_gene_variant BRCA-EU 6 31616101 31616101 single base substitution T G downstream_gene_variant BRCA-EU 6 31616101 31616101 single base substitution T G intron_variant BRCA-EU 6 31616101 31616101 single base substitution T G upstream_gene_variant BRCA-EU 6 31616174 31616174 single base substitution A T downstream_gene_variant BRCA-EU 6 31616174 31616174 single base substitution A T intron_variant BRCA-EU 6 31616174 31616174 single base substitution A T upstream_gene_variant BRCA-EU 6 31616222 31616222 single base substitution C T downstream_gene_variant BRCA-EU 6 31616222 31616222 single base substitution C T intron_variant BRCA-EU 6 31616222 31616222 single base substitution C T upstream_gene_variant BRCA-EU 6 31616638 31616638 single base substitution G C downstream_gene_variant BRCA-EU 6 31616638 31616638 single base substitution G C intron_variant BRCA-EU 6 31616638 31616638 single base substitution G C upstream_gene_variant BRCA-EU 6 31617074 31617074 single base substitution G C missense_variant H109D 325C>G BRCA-EU 6 31617074 31617074 single base substitution G C upstream_gene_variant BRCA-EU 6 31618785 31618785 single base substitution G T intron_variant BRCA-EU 6 31620452 31620452 single base substitution T A 5_prime_UTR_variant BRCA-EU 6 31620452 31620452 single base substitution T A upstream_gene_variant BRCA-EU 6 31621384 31621384 single base substitution G T upstream_gene_variant BRCA-EU 6 31625451 31625451 single base substitution G A upstream_gene_variant BRCA-FR 6 31610800 31610800 single base substitution C T downstream_gene_variant BRCA-FR 6 31610800 31610800 single base substitution C T exon_variant BRCA-FR 6 31610800 31610800 single base substitution C T intron_variant BRCA-FR 6 31610800 31610800 single base substitution C T missense_variant A175T 523G>A BRCA-FR 6 31610800 31610800 single base substitution C T missense_variant A581T 1741G>A BRCA-FR 6 31610800 31610800 single base substitution C T missense_variant A587T 1759G>A BRCA-FR 6 31610800 31610800 single base substitution C T missense_variant A617T 1849G>A BRCA-FR 6 31610800 31610800 single base substitution C T upstream_gene_variant BRCA-UK 6 31617074 31617074 single base substitution G C missense_variant H109D 325C>G BRCA-UK 6 31617074 31617074 single base substitution G C upstream_gene_variant BRCA-UK 6 31618442 31618442 single base substitution C G intron_variant BRCA-UK 6 31625193 31625193 single base substitution C T upstream_gene_variant BRCA-US 6 31602024 31602024 single base substitution A C downstream_gene_variant BRCA-US 6 31602251 31602251 single base substitution A C downstream_gene_variant BRCA-US 6 31605054 31605054 single base substitution A C downstream_gene_variant BRCA-US 6 31605345 31605345 single base substitution G T downstream_gene_variant BRCA-US 6 31608186 31608186 single base substitution T C downstream_gene_variant BRCA-US 6 31608186 31608186 single base substitution T C exon_variant BRCA-US 6 31608186 31608186 single base substitution T C intron_variant BRCA-US 6 31608186 31608186 single base substitution T C synonymous_variant E1002E 3006A>G BRCA-US 6 31608186 31608186 single base substitution T C synonymous_variant E1008E 3024A>G BRCA-US 6 31608186 31608186 single base substitution T C synonymous_variant E1038E 3114A>G BRCA-US 6 31608186 31608186 single base substitution T C synonymous_variant E150E 450A>G BRCA-US 6 31608186 31608186 single base substitution T C upstream_gene_variant BRCA-US 6 31609988 31609988 insertion of <=200bp - A downstream_gene_variant BRCA-US 6 31609988 31609988 insertion of <=200bp - A exon_variant BRCA-US 6 31609988 31609988 insertion of <=200bp - A frameshift_variant L584L? BRCA-US 6 31609988 31609988 insertion of <=200bp - A frameshift_variant L710L? BRCA-US 6 31609988 31609988 insertion of <=200bp - A frameshift_variant L716L? BRCA-US 6 31609988 31609988 insertion of <=200bp - A frameshift_variant L746L? BRCA-US 6 31609988 31609988 insertion of <=200bp - A upstream_gene_variant BRCA-US 6 31611965 31611965 single base substitution T C downstream_gene_variant BRCA-US 6 31611965 31611965 single base substitution T C exon_variant BRCA-US 6 31611965 31611965 single base substitution T C intron_variant BRCA-US 6 31611965 31611965 single base substitution T C missense_variant Q119R 356A>G BRCA-US 6 31611965 31611965 single base substitution T C missense_variant Q485R 1454A>G BRCA-US 6 31611965 31611965 single base substitution T C missense_variant Q491R 1472A>G BRCA-US 6 31611965 31611965 single base substitution T C missense_variant Q521R 1562A>G BRCA-US 6 31611965 31611965 single base substitution T C missense_variant Q79R 236A>G BRCA-US 6 31611965 31611965 single base substitution T C upstream_gene_variant BTCA-JP 6 31602915 31602915 deletion of <=200bp C - downstream_gene_variant BTCA-JP 6 31605046 31605046 single base substitution C T downstream_gene_variant BTCA-JP 6 31612913 31612913 single base substitution A G downstream_gene_variant BTCA-JP 6 31612913 31612913 single base substitution A G exon_variant BTCA-JP 6 31612913 31612913 single base substitution A G synonymous_variant N393N 1179T>C BTCA-JP 6 31612913 31612913 single base substitution A G synonymous_variant N399N 1197T>C BTCA-JP 6 31612913 31612913 single base substitution A G synonymous_variant N53N 159T>C BTCA-JP 6 31612913 31612913 single base substitution A G upstream_gene_variant BTCA-JP 6 31619325 31619325 single base substitution A G intron_variant BTCA-JP 6 31624205 31624205 single base substitution G C upstream_gene_variant CESC-US 6 31603372 31603372 single base substitution C G downstream_gene_variant CESC-US 6 31605302 31605302 single base substitution G A downstream_gene_variant CESC-US 6 31607000 31607000 single base substitution G A downstream_gene_variant CESC-US 6 31607000 31607000 single base substitution G A exon_variant CESC-US 6 31607000 31607000 single base substitution G A missense_variant R1048W 3142C>T CESC-US 6 31607000 31607000 single base substitution G A missense_variant R106W 316C>T CESC-US 6 31607000 31607000 single base substitution G A missense_variant R1097W 3289C>T CESC-US 6 31607000 31607000 single base substitution G A missense_variant R1103W 3307C>T CESC-US 6 31607000 31607000 single base substitution G A missense_variant R1133W 3397C>T CESC-US 6 31607000 31607000 single base substitution G A missense_variant R196W 586C>T CESC-US 6 31607000 31607000 single base substitution G A missense_variant R874W 2620C>T CESC-US 6 31607482 31607482 single base substitution C G downstream_gene_variant CESC-US 6 31607482 31607482 single base substitution C G exon_variant CESC-US 6 31607482 31607482 single base substitution C G intron_variant CESC-US 6 31610002 31610002 single base substitution G A downstream_gene_variant CESC-US 6 31610002 31610002 single base substitution G A exon_variant CESC-US 6 31610002 31610002 single base substitution G A missense_variant S579F 1736C>T CESC-US 6 31610002 31610002 single base substitution G A missense_variant S705F 2114C>T CESC-US 6 31610002 31610002 single base substitution G A missense_variant S711F 2132C>T CESC-US 6 31610002 31610002 single base substitution G A missense_variant S741F 2222C>T CESC-US 6 31610002 31610002 single base substitution G A upstream_gene_variant CLLE-ES 6 31625413 31625413 single base substitution C T upstream_gene_variant COAD-US 6 31602967 31602967 single base substitution G A downstream_gene_variant COAD-US 6 31603770 31603770 single base substitution A G downstream_gene_variant COAD-US 6 31603796 31603796 single base substitution G A downstream_gene_variant COAD-US 6 31604591 31604591 single base substitution C T downstream_gene_variant COAD-US 6 31604841 31604841 single base substitution C T downstream_gene_variant COAD-US 6 31605302 31605302 single base substitution G A downstream_gene_variant COAD-US 6 31608009 31608009 single base substitution G T downstream_gene_variant COAD-US 6 31608009 31608009 single base substitution G T exon_variant COAD-US 6 31608009 31608009 single base substitution G T synonymous_variant A1035A 3105C>A COAD-US 6 31608009 31608009 single base substitution G T synonymous_variant A1041A 3123C>A COAD-US 6 31608009 31608009 single base substitution G T synonymous_variant A1071A 3213C>A COAD-US 6 31608009 31608009 single base substitution G T synonymous_variant A183A 549C>A COAD-US 6 31608009 31608009 single base substitution G T synonymous_variant A861A 2583C>A COAD-US 6 31608009 31608009 single base substitution G T synonymous_variant A93A 279C>A COAD-US 6 31608009 31608009 single base substitution G T upstream_gene_variant COAD-US 6 31608463 31608463 single base substitution T C downstream_gene_variant COAD-US 6 31608463 31608463 single base substitution T C missense_variant M55V 163A>G COAD-US 6 31608463 31608463 single base substitution T C missense_variant M823V 2467A>G COAD-US 6 31608463 31608463 single base substitution T C missense_variant M949V 2845A>G COAD-US 6 31608463 31608463 single base substitution T C missense_variant M955V 2863A>G COAD-US 6 31608463 31608463 single base substitution T C missense_variant M97V 289A>G COAD-US 6 31608463 31608463 single base substitution T C missense_variant M985V 2953A>G COAD-US 6 31608463 31608463 single base substitution T C upstream_gene_variant COAD-US 6 31608571 31608571 deletion of <=200bp G - downstream_gene_variant COAD-US 6 31608571 31608571 deletion of <=200bp G - frameshift_variant Q48 COAD-US 6 31608571 31608571 deletion of <=200bp G - frameshift_variant Q816 COAD-US 6 31608571 31608571 deletion of <=200bp G - frameshift_variant Q90 COAD-US 6 31608571 31608571 deletion of <=200bp G - frameshift_variant Q942 COAD-US 6 31608571 31608571 deletion of <=200bp G - frameshift_variant Q948 COAD-US 6 31608571 31608571 deletion of <=200bp G - frameshift_variant Q978 COAD-US 6 31608571 31608571 deletion of <=200bp G - upstream_gene_variant COAD-US 6 31612849 31612849 single base substitution C T downstream_gene_variant COAD-US 6 31612849 31612849 single base substitution C T exon_variant COAD-US 6 31612849 31612849 single base substitution C T missense_variant E415K 1243G>A COAD-US 6 31612849 31612849 single base substitution C T missense_variant E421K 1261G>A COAD-US 6 31612849 31612849 single base substitution C T missense_variant E75K 223G>A COAD-US 6 31612849 31612849 single base substitution C T upstream_gene_variant COAD-US 6 31615400 31615400 single base substitution G A downstream_gene_variant COAD-US 6 31615400 31615400 single base substitution G A synonymous_variant G234G 702C>T COAD-US 6 31615400 31615400 single base substitution G A synonymous_variant G252G 756C>T COAD-US 6 31615400 31615400 single base substitution G A synonymous_variant G258G 774C>T COAD-US 6 31615400 31615400 single base substitution G A upstream_gene_variant COAD-US 6 31619438 31619438 deletion of <=200bp C - frameshift_variant A35 COCA-CN 6 31601845 31601845 single base substitution C A downstream_gene_variant COCA-CN 6 31602592 31602592 single base substitution C T downstream_gene_variant COCA-CN 6 31602651 31602651 single base substitution G T downstream_gene_variant COCA-CN 6 31603019 31603019 single base substitution T C downstream_gene_variant COCA-CN 6 31603509 31603509 single base substitution G A downstream_gene_variant COCA-CN 6 31607050 31607050 single base substitution C T downstream_gene_variant COCA-CN 6 31607050 31607050 single base substitution C T intron_variant COCA-CN 6 31607372 31607372 single base substitution C T downstream_gene_variant COCA-CN 6 31607372 31607372 single base substitution C T exon_variant COCA-CN 6 31607372 31607372 single base substitution C T intron_variant COCA-CN 6 31607372 31607372 single base substitution C T missense_variant A1064T 3190G>A COCA-CN 6 31607372 31607372 single base substitution C T missense_variant A1070T 3208G>A COCA-CN 6 31607372 31607372 single base substitution C T missense_variant A1100T 3298G>A COCA-CN 6 31609730 31609730 single base substitution A G downstream_gene_variant COCA-CN 6 31609730 31609730 single base substitution A G intron_variant COCA-CN 6 31609730 31609730 single base substitution A G splice_region_variant COCA-CN 6 31609730 31609730 single base substitution A G upstream_gene_variant COCA-CN 6 31612144 31612144 single base substitution C T downstream_gene_variant COCA-CN 6 31612144 31612144 single base substitution C T intron_variant COCA-CN 6 31612144 31612144 single base substitution C T missense_variant A499T 1495G>A COCA-CN 6 31612144 31612144 single base substitution C T upstream_gene_variant COCA-CN 6 31612448 31612448 single base substitution A C downstream_gene_variant COCA-CN 6 31612448 31612448 single base substitution A C intron_variant COCA-CN 6 31612448 31612448 single base substitution A C upstream_gene_variant COCA-CN 6 31614276 31614276 single base substitution G A downstream_gene_variant COCA-CN 6 31614276 31614276 single base substitution G A synonymous_variant V271V 813C>T COCA-CN 6 31614276 31614276 single base substitution G A synonymous_variant V277V 831C>T COCA-CN 6 31614276 31614276 single base substitution G A upstream_gene_variant COCA-CN 6 31614543 31614543 single base substitution G T downstream_gene_variant COCA-CN 6 31614543 31614543 single base substitution G T intron_variant COCA-CN 6 31614543 31614543 single base substitution G T upstream_gene_variant COCA-CN 6 31616366 31616366 single base substitution G A downstream_gene_variant COCA-CN 6 31616366 31616366 single base substitution G A intron_variant COCA-CN 6 31616366 31616366 single base substitution G A upstream_gene_variant COCA-CN 6 31616501 31616501 single base substitution C T downstream_gene_variant COCA-CN 6 31616501 31616501 single base substitution C T missense_variant A151T 451G>A COCA-CN 6 31616501 31616501 single base substitution C T missense_variant A169T 505G>A COCA-CN 6 31616501 31616501 single base substitution C T upstream_gene_variant COCA-CN 6 31617020 31617020 single base substitution G A missense_variant R127W 379C>T COCA-CN 6 31617020 31617020 single base substitution G A upstream_gene_variant COCA-CN 6 31619301 31619301 single base substitution G A intron_variant COCA-CN 6 31620126 31620126 single base substitution A C 5_prime_UTR_variant COCA-CN 6 31620126 31620126 single base substitution A C intron_variant COCA-CN 6 31620126 31620126 single base substitution A C upstream_gene_variant COCA-CN 6 31625422 31625422 single base substitution G A upstream_gene_variant ESAD-UK 6 31602714 31602714 single base substitution C T downstream_gene_variant ESAD-UK 6 31603931 31603931 single base substitution G A downstream_gene_variant ESAD-UK 6 31612788 31612788 single base substitution G A downstream_gene_variant ESAD-UK 6 31612788 31612788 single base substitution G A exon_variant ESAD-UK 6 31612788 31612788 single base substitution G A missense_variant P20L 59C>T ESAD-UK 6 31612788 31612788 single base substitution G A missense_variant P435L 1304C>T ESAD-UK 6 31612788 31612788 single base substitution G A missense_variant P441L 1322C>T ESAD-UK 6 31612788 31612788 single base substitution G A missense_variant P95L 284C>T ESAD-UK 6 31612788 31612788 single base substitution G A upstream_gene_variant ESAD-UK 6 31613363 31613363 single base substitution C T downstream_gene_variant ESAD-UK 6 31613363 31613363 single base substitution C T missense_variant D313N 937G>A ESAD-UK 6 31613363 31613363 single base substitution C T missense_variant D319N 955G>A ESAD-UK 6 31613363 31613363 single base substitution C T upstream_gene_variant ESAD-UK 6 31616953 31616953 single base substitution T C intron_variant ESAD-UK 6 31616953 31616953 single base substitution T C upstream_gene_variant ESAD-UK 6 31617341 31617341 single base substitution G A missense_variant R58W 172C>T ESAD-UK 6 31617341 31617341 single base substitution G A upstream_gene_variant ESAD-UK 6 31618075 31618075 single base substitution C T intron_variant ESAD-UK 6 31618075 31618075 single base substitution C T upstream_gene_variant ESAD-UK 6 31620249 31620249 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 6 31620249 31620249 single base substitution G C intron_variant ESAD-UK 6 31620249 31620249 single base substitution G C upstream_gene_variant ESAD-UK 6 31624324 31624324 single base substitution G T upstream_gene_variant KIRC-US 6 31609641 31609641 insertion of <=200bp - G downstream_gene_variant KIRC-US 6 31609641 31609641 insertion of <=200bp - G exon_variant KIRC-US 6 31609641 31609641 insertion of <=200bp - G frameshift_variant Q644H? KIRC-US 6 31609641 31609641 insertion of <=200bp - G frameshift_variant Q770H? KIRC-US 6 31609641 31609641 insertion of <=200bp - G frameshift_variant Q776H? KIRC-US 6 31609641 31609641 insertion of <=200bp - G frameshift_variant Q806H? KIRC-US 6 31609641 31609641 insertion of <=200bp - G upstream_gene_variant KIRC-US 6 31610686 31610686 single base substitution A G downstream_gene_variant KIRC-US 6 31610686 31610686 single base substitution A G exon_variant KIRC-US 6 31610686 31610686 single base substitution A G intron_variant KIRC-US 6 31610686 31610686 single base substitution A G missense_variant S213P 637T>C KIRC-US 6 31610686 31610686 single base substitution A G missense_variant S619P 1855T>C KIRC-US 6 31610686 31610686 single base substitution A G missense_variant S625P 1873T>C KIRC-US 6 31610686 31610686 single base substitution A G missense_variant S655P 1963T>C KIRC-US 6 31610686 31610686 single base substitution A G upstream_gene_variant KIRC-US 6 31611899 31611899 single base substitution C A downstream_gene_variant KIRC-US 6 31611899 31611899 single base substitution C A exon_variant KIRC-US 6 31611899 31611899 single base substitution C A intron_variant KIRC-US 6 31611899 31611899 single base substitution C A missense_variant R101L 302G>T KIRC-US 6 31611899 31611899 single base substitution C A missense_variant R141L 422G>T KIRC-US 6 31611899 31611899 single base substitution C A missense_variant R507L 1520G>T KIRC-US 6 31611899 31611899 single base substitution C A missense_variant R513L 1538G>T KIRC-US 6 31611899 31611899 single base substitution C A missense_variant R543L 1628G>T KIRC-US 6 31611899 31611899 single base substitution C A upstream_gene_variant KIRP-US 6 31605276 31605276 single base substitution G A downstream_gene_variant KIRP-US 6 31612378 31612378 single base substitution A T downstream_gene_variant KIRP-US 6 31612378 31612378 single base substitution A T intron_variant KIRP-US 6 31612378 31612378 single base substitution A T missense_variant D457E 1371T>A KIRP-US 6 31612378 31612378 single base substitution A T missense_variant D463E 1389T>A KIRP-US 6 31612378 31612378 single base substitution A T missense_variant D51E 153T>A KIRP-US 6 31612378 31612378 single base substitution A T splice_region_variant KIRP-US 6 31612378 31612378 single base substitution A T upstream_gene_variant KIRP-US 6 31625014 31625014 single base substitution C G upstream_gene_variant LAML-KR 6 31602244 31602244 single base substitution T C downstream_gene_variant LAML-KR 6 31619652 31619652 single base substitution T A 5_prime_UTR_variant LAML-KR 6 31619652 31619652 single base substitution T A intron_variant LGG-US 6 31612853 31612853 single base substitution A C downstream_gene_variant LGG-US 6 31612853 31612853 single base substitution A C exon_variant LGG-US 6 31612853 31612853 single base substitution A C missense_variant N413K 1239T>G LGG-US 6 31612853 31612853 single base substitution A C missense_variant N419K 1257T>G LGG-US 6 31612853 31612853 single base substitution A C missense_variant N73K 219T>G LGG-US 6 31612853 31612853 single base substitution A C upstream_gene_variant LICA-CN 6 31602696 31602696 single base substitution C T downstream_gene_variant LICA-CN 6 31604715 31604715 single base substitution G T downstream_gene_variant LICA-CN 6 31611684 31611684 single base substitution A G downstream_gene_variant LICA-CN 6 31611684 31611684 single base substitution A G exon_variant LICA-CN 6 31611684 31611684 single base substitution A G missense_variant M138T 413T>C LICA-CN 6 31611684 31611684 single base substitution A G missense_variant M178T 533T>C LICA-CN 6 31611684 31611684 single base substitution A G missense_variant M543T 1628T>C LICA-CN 6 31611684 31611684 single base substitution A G missense_variant M544T 1631T>C LICA-CN 6 31611684 31611684 single base substitution A G missense_variant M550T 1649T>C LICA-CN 6 31611684 31611684 single base substitution A G missense_variant M580T 1739T>C LICA-CN 6 31611684 31611684 single base substitution A G upstream_gene_variant LICA-CN 6 31617044 31617044 single base substitution C A missense_variant G119W 355G>T LICA-CN 6 31617044 31617044 single base substitution C A upstream_gene_variant LICA-CN 6 31617396 31617396 single base substitution T C synonymous_variant V39V 117A>G LICA-CN 6 31617396 31617396 single base substitution T C upstream_gene_variant LICA-FR 6 31605097 31605097 single base substitution A C downstream_gene_variant LICA-FR 6 31605341 31605341 single base substitution C A downstream_gene_variant LICA-FR 6 31609859 31609859 single base substitution G C downstream_gene_variant LICA-FR 6 31609859 31609859 single base substitution G C intron_variant LICA-FR 6 31609859 31609859 single base substitution G C upstream_gene_variant LICA-FR 6 31622179 31622179 single base substitution A C upstream_gene_variant LICA-FR 6 31625259 31625261 deletion of <=200bp AGT - upstream_gene_variant LICA-FR 6 31625422 31625422 single base substitution G A upstream_gene_variant LIHC-US 6 31608198 31608198 single base substitution T A downstream_gene_variant LIHC-US 6 31608198 31608198 single base substitution T A exon_variant LIHC-US 6 31608198 31608198 single base substitution T A intron_variant LIHC-US 6 31608198 31608198 single base substitution T A synonymous_variant S1004S 3012A>T LIHC-US 6 31608198 31608198 single base substitution T A synonymous_variant S1034S 3102A>T LIHC-US 6 31608198 31608198 single base substitution T A synonymous_variant S146S 438A>T LIHC-US 6 31608198 31608198 single base substitution T A synonymous_variant S998S 2994A>T LIHC-US 6 31608198 31608198 single base substitution T A upstream_gene_variant LIHC-US 6 31608213 31608213 single base substitution T C downstream_gene_variant LIHC-US 6 31608213 31608213 single base substitution T C exon_variant LIHC-US 6 31608213 31608213 single base substitution T C intron_variant LIHC-US 6 31608213 31608213 single base substitution T C synonymous_variant E1029E 3087A>G LIHC-US 6 31608213 31608213 single base substitution T C synonymous_variant E141E 423A>G LIHC-US 6 31608213 31608213 single base substitution T C synonymous_variant E993E 2979A>G LIHC-US 6 31608213 31608213 single base substitution T C synonymous_variant E999E 2997A>G LIHC-US 6 31608213 31608213 single base substitution T C upstream_gene_variant LIHC-US 6 31610072 31610072 single base substitution G A downstream_gene_variant LIHC-US 6 31610072 31610072 single base substitution G A exon_variant LIHC-US 6 31610072 31610072 single base substitution G A missense_variant P556S 1666C>T LIHC-US 6 31610072 31610072 single base substitution G A missense_variant P682S 2044C>T LIHC-US 6 31610072 31610072 single base substitution G A missense_variant P688S 2062C>T LIHC-US 6 31610072 31610072 single base substitution G A missense_variant P718S 2152C>T LIHC-US 6 31610072 31610072 single base substitution G A upstream_gene_variant LIHC-US 6 31610118 31610118 single base substitution C A downstream_gene_variant LIHC-US 6 31610118 31610118 single base substitution C A exon_variant LIHC-US 6 31610118 31610118 single base substitution C A intron_variant LIHC-US 6 31610118 31610118 single base substitution C A missense_variant Q666H 1998G>T LIHC-US 6 31610118 31610118 single base substitution C A missense_variant Q672H 2016G>T LIHC-US 6 31610118 31610118 single base substitution C A missense_variant Q702H 2106G>T LIHC-US 6 31610118 31610118 single base substitution C A upstream_gene_variant LIHC-US 6 31610883 31610883 single base substitution G A downstream_gene_variant LIHC-US 6 31610883 31610883 single base substitution G A exon_variant LIHC-US 6 31610883 31610883 single base substitution G A missense_variant T147I 440C>T LIHC-US 6 31610883 31610883 single base substitution G A missense_variant T552I 1655C>T LIHC-US 6 31610883 31610883 single base substitution G A missense_variant T553I 1658C>T LIHC-US 6 31610883 31610883 single base substitution G A missense_variant T559I 1676C>T LIHC-US 6 31610883 31610883 single base substitution G A missense_variant T589I 1766C>T LIHC-US 6 31610883 31610883 single base substitution G A upstream_gene_variant LIHC-US 6 31623826 31623826 single base substitution A C upstream_gene_variant LINC-JP 6 31602844 31602844 single base substitution C G downstream_gene_variant LINC-JP 6 31604957 31604957 single base substitution T G downstream_gene_variant LINC-JP 6 31608437 31608437 single base substitution A C downstream_gene_variant LINC-JP 6 31608437 31608437 single base substitution A C synonymous_variant A105A 315T>G LINC-JP 6 31608437 31608437 single base substitution A C synonymous_variant A63A 189T>G LINC-JP 6 31608437 31608437 single base substitution A C synonymous_variant A831A 2493T>G LINC-JP 6 31608437 31608437 single base substitution A C synonymous_variant A957A 2871T>G LINC-JP 6 31608437 31608437 single base substitution A C synonymous_variant A963A 2889T>G LINC-JP 6 31608437 31608437 single base substitution A C synonymous_variant A993A 2979T>G LINC-JP 6 31608437 31608437 single base substitution A C upstream_gene_variant LINC-JP 6 31608742 31608742 single base substitution C A downstream_gene_variant LINC-JP 6 31608742 31608742 single base substitution C A exon_variant LINC-JP 6 31608742 31608742 single base substitution C A intron_variant LINC-JP 6 31608742 31608742 single base substitution C A upstream_gene_variant LINC-JP 6 31609213 31609213 single base substitution T A downstream_gene_variant LINC-JP 6 31609213 31609213 single base substitution T A exon_variant LINC-JP 6 31609213 31609213 single base substitution T A intron_variant LINC-JP 6 31609213 31609213 single base substitution T A upstream_gene_variant LINC-JP 6 31613293 31613293 single base substitution T A downstream_gene_variant LINC-JP 6 31613293 31613293 single base substitution T A exon_variant LINC-JP 6 31613293 31613293 single base substitution T A missense_variant D336V 1007A>T LINC-JP 6 31613293 31613293 single base substitution T A missense_variant D342V 1025A>T LINC-JP 6 31613293 31613293 single base substitution T A upstream_gene_variant LINC-JP 6 31613601 31613601 single base substitution T C downstream_gene_variant LINC-JP 6 31613601 31613601 single base substitution T C intron_variant LINC-JP 6 31613601 31613601 single base substitution T C upstream_gene_variant LINC-JP 6 31624186 31624186 deletion of <=200bp A - upstream_gene_variant LINC-JP 6 31625067 31625067 single base substitution G C upstream_gene_variant LIRI-JP 6 31602021 31602021 single base substitution G A downstream_gene_variant LIRI-JP 6 31604503 31604503 single base substitution G T downstream_gene_variant LIRI-JP 6 31605879 31605879 single base substitution T G downstream_gene_variant LIRI-JP 6 31606278 31606278 deletion of <=200bp G - downstream_gene_variant LIRI-JP 6 31607641 31607641 single base substitution T C downstream_gene_variant LIRI-JP 6 31607641 31607641 single base substitution T C intron_variant LIRI-JP 6 31607641 31607641 single base substitution T C upstream_gene_variant LIRI-JP 6 31607700 31607700 single base substitution A C downstream_gene_variant LIRI-JP 6 31607700 31607700 single base substitution A C intron_variant LIRI-JP 6 31607700 31607700 single base substitution A C upstream_gene_variant LIRI-JP 6 31610190 31610193 deletion of <=200bp AAAG - downstream_gene_variant LIRI-JP 6 31610190 31610193 deletion of <=200bp AAAG - intron_variant LIRI-JP 6 31610190 31610193 deletion of <=200bp AAAG - upstream_gene_variant LIRI-JP 6 31611473 31611473 single base substitution C T downstream_gene_variant LIRI-JP 6 31611473 31611473 single base substitution C T intron_variant LIRI-JP 6 31611473 31611473 single base substitution C T upstream_gene_variant LIRI-JP 6 31611558 31611558 single base substitution C A downstream_gene_variant LIRI-JP 6 31611558 31611558 single base substitution C A intron_variant LIRI-JP 6 31611558 31611558 single base substitution C A upstream_gene_variant LIRI-JP 6 31613855 31613855 single base substitution C T downstream_gene_variant LIRI-JP 6 31613855 31613855 single base substitution C T intron_variant LIRI-JP 6 31613855 31613855 single base substitution C T upstream_gene_variant LIRI-JP 6 31616312 31616312 single base substitution C A downstream_gene_variant LIRI-JP 6 31616312 31616312 single base substitution C A intron_variant LIRI-JP 6 31616312 31616312 single base substitution C A upstream_gene_variant LIRI-JP 6 31620853 31620878 deletion of <=200bp CGGGTGGGCGTTTTAAGGGCTGTGGG - upstream_gene_variant LIRI-JP 6 31622502 31622502 single base substitution C T upstream_gene_variant LIRI-JP 6 31623349 31623349 single base substitution G C upstream_gene_variant LIRI-JP 6 31623451 31623451 single base substitution C T upstream_gene_variant LIRI-JP 6 31623521 31623521 single base substitution A T upstream_gene_variant LIRI-JP 6 31623731 31623731 single base substitution C T upstream_gene_variant LIRI-JP 6 31624000 31624000 single base substitution A G upstream_gene_variant LIRI-JP 6 31624456 31624456 single base substitution T C upstream_gene_variant LUSC-KR 6 31601843 31601843 single base substitution T C downstream_gene_variant LUSC-KR 6 31602707 31602707 single base substitution G C downstream_gene_variant LUSC-KR 6 31602967 31602967 single base substitution G A downstream_gene_variant LUSC-KR 6 31603770 31603770 single base substitution A G downstream_gene_variant LUSC-KR 6 31603884 31603884 single base substitution G A downstream_gene_variant LUSC-KR 6 31604591 31604591 single base substitution C T downstream_gene_variant LUSC-KR 6 31604921 31604921 single base substitution G A downstream_gene_variant LUSC-KR 6 31607942 31607942 single base substitution T C downstream_gene_variant LUSC-KR 6 31607942 31607942 single base substitution T C intron_variant LUSC-KR 6 31607942 31607942 single base substitution T C upstream_gene_variant LUSC-KR 6 31609272 31609272 single base substitution T C downstream_gene_variant LUSC-KR 6 31609272 31609272 single base substitution T C exon_variant LUSC-KR 6 31609272 31609272 single base substitution T C intron_variant LUSC-KR 6 31609272 31609272 single base substitution T C upstream_gene_variant LUSC-KR 6 31609676 31609676 single base substitution C A downstream_gene_variant LUSC-KR 6 31609676 31609676 single base substitution C A exon_variant LUSC-KR 6 31609676 31609676 single base substitution C A missense_variant M632I 1896G>T LUSC-KR 6 31609676 31609676 single base substitution C A missense_variant M758I 2274G>T LUSC-KR 6 31609676 31609676 single base substitution C A missense_variant M764I 2292G>T LUSC-KR 6 31609676 31609676 single base substitution C A missense_variant M794I 2382G>T LUSC-KR 6 31609676 31609676 single base substitution C A upstream_gene_variant LUSC-KR 6 31611840 31611840 single base substitution C A downstream_gene_variant LUSC-KR 6 31611840 31611840 single base substitution C A intron_variant LUSC-KR 6 31611840 31611840 single base substitution C A upstream_gene_variant LUSC-KR 6 31616366 31616366 single base substitution G A downstream_gene_variant LUSC-KR 6 31616366 31616366 single base substitution G A intron_variant LUSC-KR 6 31616366 31616366 single base substitution G A upstream_gene_variant LUSC-KR 6 31618497 31618497 single base substitution C T intron_variant LUSC-KR 6 31618590 31618590 single base substitution G C intron_variant LUSC-KR 6 31619554 31619554 single base substitution C G 5_prime_UTR_variant LUSC-KR 6 31619554 31619554 single base substitution C G splice_acceptor_variant LUSC-KR 6 31619576 31619576 single base substitution A G 5_prime_UTR_variant LUSC-KR 6 31619576 31619576 single base substitution A G intron_variant LUSC-US 6 31603799 31603799 single base substitution C T downstream_gene_variant LUSC-US 6 31607333 31607333 single base substitution C T downstream_gene_variant LUSC-US 6 31607333 31607333 single base substitution C T exon_variant LUSC-US 6 31607333 31607333 single base substitution C T intron_variant LUSC-US 6 31607333 31607333 single base substitution C T missense_variant E1077K 3229G>A LUSC-US 6 31607333 31607333 single base substitution C T missense_variant E1083K 3247G>A LUSC-US 6 31607333 31607333 single base substitution C T missense_variant E1113K 3337G>A LUSC-US 6 31608925 31608925 single base substitution C A downstream_gene_variant LUSC-US 6 31608925 31608925 single base substitution C A exon_variant LUSC-US 6 31608925 31608925 single base substitution C A missense_variant G27W 79G>T LUSC-US 6 31608925 31608925 single base substitution C A missense_variant G753W 2257G>T LUSC-US 6 31608925 31608925 single base substitution C A missense_variant G879W 2635G>T LUSC-US 6 31608925 31608925 single base substitution C A missense_variant G885W 2653G>T LUSC-US 6 31608925 31608925 single base substitution C A missense_variant G915W 2743G>T LUSC-US 6 31608925 31608925 single base substitution C A upstream_gene_variant LUSC-US 6 31609651 31609651 single base substitution C A downstream_gene_variant LUSC-US 6 31609651 31609651 single base substitution C A exon_variant LUSC-US 6 31609651 31609651 single base substitution C A missense_variant G641W 1921G>T LUSC-US 6 31609651 31609651 single base substitution C A missense_variant G767W 2299G>T LUSC-US 6 31609651 31609651 single base substitution C A missense_variant G773W 2317G>T LUSC-US 6 31609651 31609651 single base substitution C A missense_variant G803W 2407G>T LUSC-US 6 31609651 31609651 single base substitution C A upstream_gene_variant LUSC-US 6 31624395 31624395 single base substitution C A upstream_gene_variant MALY-DE 6 31610190 31610193 deletion of <=200bp AAAG - downstream_gene_variant MALY-DE 6 31610190 31610193 deletion of <=200bp AAAG - intron_variant MALY-DE 6 31610190 31610193 deletion of <=200bp AAAG - upstream_gene_variant MALY-DE 6 31622567 31622567 single base substitution C T upstream_gene_variant MALY-DE 6 31623260 31623260 single base substitution T C upstream_gene_variant MALY-DE 6 31623724 31623724 single base substitution C T upstream_gene_variant MELA-AU 6 31601954 31601954 single base substitution C T downstream_gene_variant MELA-AU 6 31602053 31602053 single base substitution C T downstream_gene_variant MELA-AU 6 31602293 31602293 single base substitution A G downstream_gene_variant MELA-AU 6 31603451 31603451 single base substitution C T downstream_gene_variant MELA-AU 6 31603504 31603504 single base substitution G T downstream_gene_variant MELA-AU 6 31605356 31605356 single base substitution C T downstream_gene_variant MELA-AU 6 31606329 31606329 single base substitution G A downstream_gene_variant MELA-AU 6 31606579 31606579 single base substitution C T downstream_gene_variant MELA-AU 6 31606581 31606581 single base substitution T C downstream_gene_variant MELA-AU 6 31607320 31607320 single base substitution C G downstream_gene_variant MELA-AU 6 31607320 31607320 single base substitution C G exon_variant MELA-AU 6 31607320 31607320 single base substitution C G intron_variant MELA-AU 6 31607320 31607320 single base substitution C G missense_variant R1081P 3242G>C MELA-AU 6 31607320 31607320 single base substitution C G missense_variant R1087P 3260G>C MELA-AU 6 31607320 31607320 single base substitution C G missense_variant R1117P 3350G>C MELA-AU 6 31607704 31607704 single base substitution G A downstream_gene_variant MELA-AU 6 31607704 31607704 single base substitution G A intron_variant MELA-AU 6 31607704 31607704 single base substitution G A upstream_gene_variant MELA-AU 6 31608097 31608097 single base substitution G A downstream_gene_variant MELA-AU 6 31608097 31608097 single base substitution G A intron_variant MELA-AU 6 31608097 31608097 single base substitution G A upstream_gene_variant MELA-AU 6 31608222 31608222 single base substitution G A downstream_gene_variant MELA-AU 6 31608222 31608222 single base substitution G A exon_variant MELA-AU 6 31608222 31608222 single base substitution G A intron_variant MELA-AU 6 31608222 31608222 single base substitution G A synonymous_variant S1026S 3078C>T MELA-AU 6 31608222 31608222 single base substitution G A synonymous_variant S138S 414C>T MELA-AU 6 31608222 31608222 single base substitution G A synonymous_variant S990S 2970C>T MELA-AU 6 31608222 31608222 single base substitution G A synonymous_variant S996S 2988C>T MELA-AU 6 31608222 31608222 single base substitution G A upstream_gene_variant MELA-AU 6 31608236 31608236 single base substitution G A downstream_gene_variant MELA-AU 6 31608236 31608236 single base substitution G A exon_variant MELA-AU 6 31608236 31608236 single base substitution G A intron_variant MELA-AU 6 31608236 31608236 single base substitution G A missense_variant P1022S 3064C>T MELA-AU 6 31608236 31608236 single base substitution G A missense_variant P134S 400C>T MELA-AU 6 31608236 31608236 single base substitution G A missense_variant P986S 2956C>T MELA-AU 6 31608236 31608236 single base substitution G A missense_variant P992S 2974C>T MELA-AU 6 31608236 31608236 single base substitution G A upstream_gene_variant MELA-AU 6 31608495 31608495 single base substitution G A downstream_gene_variant MELA-AU 6 31608495 31608495 single base substitution G A intron_variant MELA-AU 6 31608495 31608495 single base substitution G A upstream_gene_variant MELA-AU 6 31608537 31608537 single base substitution A G downstream_gene_variant MELA-AU 6 31608537 31608537 single base substitution A G intron_variant MELA-AU 6 31608537 31608537 single base substitution A G upstream_gene_variant MELA-AU 6 31609197 31609197 single base substitution G A downstream_gene_variant MELA-AU 6 31609197 31609197 single base substitution G A exon_variant MELA-AU 6 31609197 31609197 single base substitution G A splice_region_variant MELA-AU 6 31609197 31609197 single base substitution G A upstream_gene_variant MELA-AU 6 31609466 31609466 single base substitution G A downstream_gene_variant MELA-AU 6 31609466 31609466 single base substitution G A intron_variant MELA-AU 6 31609466 31609466 single base substitution G A upstream_gene_variant MELA-AU 6 31610001 31610001 single base substitution G A downstream_gene_variant MELA-AU 6 31610001 31610001 single base substitution G A exon_variant MELA-AU 6 31610001 31610001 single base substitution G A synonymous_variant S579S 1737C>T MELA-AU 6 31610001 31610001 single base substitution G A synonymous_variant S705S 2115C>T MELA-AU 6 31610001 31610001 single base substitution G A synonymous_variant S711S 2133C>T MELA-AU 6 31610001 31610001 single base substitution G A synonymous_variant S741S 2223C>T MELA-AU 6 31610001 31610001 single base substitution G A upstream_gene_variant MELA-AU 6 31610697 31610697 single base substitution C T downstream_gene_variant MELA-AU 6 31610697 31610697 single base substitution C T exon_variant MELA-AU 6 31610697 31610697 single base substitution C T intron_variant MELA-AU 6 31610697 31610697 single base substitution C T missense_variant G209E 626G>A MELA-AU 6 31610697 31610697 single base substitution C T missense_variant G615E 1844G>A MELA-AU 6 31610697 31610697 single base substitution C T missense_variant G621E 1862G>A MELA-AU 6 31610697 31610697 single base substitution C T missense_variant G651E 1952G>A MELA-AU 6 31610697 31610697 single base substitution C T upstream_gene_variant MELA-AU 6 31610962 31610962 single base substitution G A downstream_gene_variant MELA-AU 6 31610962 31610962 single base substitution G A intron_variant MELA-AU 6 31610962 31610962 single base substitution G A upstream_gene_variant MELA-AU 6 31611123 31611124 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 6 31611123 31611124 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 31611123 31611124 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 6 31611364 31611364 single base substitution G A downstream_gene_variant MELA-AU 6 31611364 31611364 single base substitution G A intron_variant MELA-AU 6 31611364 31611364 single base substitution G A upstream_gene_variant MELA-AU 6 31611488 31611488 single base substitution G A downstream_gene_variant MELA-AU 6 31611488 31611488 single base substitution G A intron_variant MELA-AU 6 31611488 31611488 single base substitution G A upstream_gene_variant MELA-AU 6 31611951 31611951 single base substitution G A downstream_gene_variant MELA-AU 6 31611951 31611951 single base substitution G A exon_variant MELA-AU 6 31611951 31611951 single base substitution G A intron_variant MELA-AU 6 31611951 31611951 single base substitution G A missense_variant P124S 370C>T MELA-AU 6 31611951 31611951 single base substitution G A missense_variant P490S 1468C>T MELA-AU 6 31611951 31611951 single base substitution G A missense_variant P496S 1486C>T MELA-AU 6 31611951 31611951 single base substitution G A missense_variant P526S 1576C>T MELA-AU 6 31611951 31611951 single base substitution G A missense_variant P84S 250C>T MELA-AU 6 31611951 31611951 single base substitution G A upstream_gene_variant MELA-AU 6 31611987 31611987 single base substitution G A downstream_gene_variant MELA-AU 6 31611987 31611987 single base substitution G A exon_variant MELA-AU 6 31611987 31611987 single base substitution G A intron_variant MELA-AU 6 31611987 31611987 single base substitution G A upstream_gene_variant MELA-AU 6 31612333 31612333 single base substitution G A downstream_gene_variant MELA-AU 6 31612333 31612333 single base substitution G A exon_variant MELA-AU 6 31612333 31612333 single base substitution G A intron_variant MELA-AU 6 31612333 31612333 single base substitution G A synonymous_variant P472P 1416C>T MELA-AU 6 31612333 31612333 single base substitution G A synonymous_variant P478P 1434C>T MELA-AU 6 31612333 31612333 single base substitution G A synonymous_variant P66P 198C>T MELA-AU 6 31612333 31612333 single base substitution G A upstream_gene_variant MELA-AU 6 31612420 31612420 single base substitution G A downstream_gene_variant MELA-AU 6 31612420 31612420 single base substitution G A intron_variant MELA-AU 6 31612420 31612420 single base substitution G A upstream_gene_variant MELA-AU 6 31612529 31612530 multiple base substitution (>=2bp and <=200bp) CA AC downstream_gene_variant MELA-AU 6 31612529 31612530 multiple base substitution (>=2bp and <=200bp) CA AC intron_variant MELA-AU 6 31612529 31612530 multiple base substitution (>=2bp and <=200bp) CA AC upstream_gene_variant MELA-AU 6 31612890 31612890 single base substitution G A downstream_gene_variant MELA-AU 6 31612890 31612890 single base substitution G A exon_variant MELA-AU 6 31612890 31612890 single base substitution G A missense_variant P401L 1202C>T MELA-AU 6 31612890 31612890 single base substitution G A missense_variant P407L 1220C>T MELA-AU 6 31612890 31612890 single base substitution G A missense_variant P61L 182C>T MELA-AU 6 31612890 31612890 single base substitution G A upstream_gene_variant MELA-AU 6 31612900 31612900 single base substitution G T downstream_gene_variant MELA-AU 6 31612900 31612900 single base substitution G T exon_variant MELA-AU 6 31612900 31612900 single base substitution G T missense_variant P398T 1192C>A MELA-AU 6 31612900 31612900 single base substitution G T missense_variant P404T 1210C>A MELA-AU 6 31612900 31612900 single base substitution G T missense_variant P58T 172C>A MELA-AU 6 31612900 31612900 single base substitution G T upstream_gene_variant MELA-AU 6 31612918 31612918 single base substitution G A downstream_gene_variant MELA-AU 6 31612918 31612918 single base substitution G A exon_variant MELA-AU 6 31612918 31612918 single base substitution G A missense_variant P392S 1174C>T MELA-AU 6 31612918 31612918 single base substitution G A missense_variant P398S 1192C>T MELA-AU 6 31612918 31612918 single base substitution G A missense_variant P52S 154C>T MELA-AU 6 31612918 31612918 single base substitution G A upstream_gene_variant MELA-AU 6 31612927 31612927 single base substitution G A downstream_gene_variant MELA-AU 6 31612927 31612927 single base substitution G A exon_variant MELA-AU 6 31612927 31612927 single base substitution G A missense_variant P389S 1165C>T MELA-AU 6 31612927 31612927 single base substitution G A missense_variant P395S 1183C>T MELA-AU 6 31612927 31612927 single base substitution G A missense_variant P49S 145C>T MELA-AU 6 31612927 31612927 single base substitution G A upstream_gene_variant MELA-AU 6 31613705 31613705 single base substitution G A downstream_gene_variant MELA-AU 6 31613705 31613705 single base substitution G A intron_variant MELA-AU 6 31613705 31613705 single base substitution G A upstream_gene_variant MELA-AU 6 31613706 31613706 single base substitution G A downstream_gene_variant MELA-AU 6 31613706 31613706 single base substitution G A intron_variant MELA-AU 6 31613706 31613706 single base substitution G A upstream_gene_variant MELA-AU 6 31614092 31614092 single base substitution G A downstream_gene_variant MELA-AU 6 31614092 31614092 single base substitution G A intron_variant MELA-AU 6 31614092 31614092 single base substitution G A upstream_gene_variant MELA-AU 6 31614152 31614152 single base substitution G A downstream_gene_variant MELA-AU 6 31614152 31614152 single base substitution G A intron_variant MELA-AU 6 31614152 31614152 single base substitution G A upstream_gene_variant MELA-AU 6 31614390 31614391 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 6 31614390 31614391 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 6 31614390 31614391 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 6 31614656 31614656 single base substitution T G downstream_gene_variant MELA-AU 6 31614656 31614656 single base substitution T G intron_variant MELA-AU 6 31614656 31614656 single base substitution T G upstream_gene_variant MELA-AU 6 31614890 31614890 single base substitution G A downstream_gene_variant MELA-AU 6 31614890 31614890 single base substitution G A intron_variant MELA-AU 6 31614890 31614890 single base substitution G A upstream_gene_variant MELA-AU 6 31614991 31614991 single base substitution T C downstream_gene_variant MELA-AU 6 31614991 31614991 single base substitution T C intron_variant MELA-AU 6 31614991 31614991 single base substitution T C upstream_gene_variant MELA-AU 6 31615171 31615171 single base substitution G A downstream_gene_variant MELA-AU 6 31615171 31615171 single base substitution G A intron_variant MELA-AU 6 31615171 31615171 single base substitution G A upstream_gene_variant MELA-AU 6 31615300 31615300 single base substitution G A downstream_gene_variant MELA-AU 6 31615300 31615300 single base substitution G A intron_variant MELA-AU 6 31615300 31615300 single base substitution G A upstream_gene_variant MELA-AU 6 31615588 31615588 single base substitution G A downstream_gene_variant MELA-AU 6 31615588 31615588 single base substitution G A stop_gained Q172* 514C>T MELA-AU 6 31615588 31615588 single base substitution G A stop_gained Q190* 568C>T MELA-AU 6 31615588 31615588 single base substitution G A stop_gained Q196* 586C>T MELA-AU 6 31615588 31615588 single base substitution G A upstream_gene_variant MELA-AU 6 31616402 31616402 single base substitution G A downstream_gene_variant MELA-AU 6 31616402 31616402 single base substitution G A intron_variant MELA-AU 6 31616402 31616402 single base substitution G A upstream_gene_variant MELA-AU 6 31616746 31616746 single base substitution G A intron_variant MELA-AU 6 31616746 31616746 single base substitution G A splice_region_variant MELA-AU 6 31616746 31616746 single base substitution G A upstream_gene_variant MELA-AU 6 31617056 31617056 single base substitution G A missense_variant P115S 343C>T MELA-AU 6 31617056 31617056 single base substitution G A upstream_gene_variant MELA-AU 6 31617116 31617116 single base substitution G A missense_variant P95S 283C>T MELA-AU 6 31617116 31617116 single base substitution G A upstream_gene_variant MELA-AU 6 31617745 31617745 single base substitution G A intron_variant MELA-AU 6 31617745 31617745 single base substitution G A upstream_gene_variant MELA-AU 6 31617918 31617918 single base substitution G A intron_variant MELA-AU 6 31617918 31617918 single base substitution G A upstream_gene_variant MELA-AU 6 31617988 31617988 single base substitution C A intron_variant MELA-AU 6 31617988 31617988 single base substitution C A upstream_gene_variant MELA-AU 6 31618185 31618185 single base substitution T A intron_variant MELA-AU 6 31618185 31618185 single base substitution T A upstream_gene_variant MELA-AU 6 31618739 31618739 single base substitution G A intron_variant MELA-AU 6 31618773 31618773 single base substitution G A intron_variant MELA-AU 6 31619012 31619012 single base substitution G A intron_variant MELA-AU 6 31619803 31619803 single base substitution A G 5_prime_UTR_variant MELA-AU 6 31619803 31619803 single base substitution A G intron_variant MELA-AU 6 31619803 31619803 single base substitution A G upstream_gene_variant MELA-AU 6 31619806 31619806 single base substitution G A 5_prime_UTR_variant MELA-AU 6 31619806 31619806 single base substitution G A intron_variant MELA-AU 6 31619806 31619806 single base substitution G A upstream_gene_variant MELA-AU 6 31622495 31622495 single base substitution G A upstream_gene_variant MELA-AU 6 31622959 31622959 single base substitution C T upstream_gene_variant MELA-AU 6 31623021 31623021 single base substitution G A upstream_gene_variant MELA-AU 6 31623925 31623925 single base substitution G A upstream_gene_variant MELA-AU 6 31624061 31624062 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 6 31624266 31624266 single base substitution G A upstream_gene_variant MELA-AU 6 31625052 31625052 single base substitution G A upstream_gene_variant MELA-AU 6 31625290 31625290 single base substitution G A upstream_gene_variant ORCA-IN 6 31604841 31604841 single base substitution C T downstream_gene_variant ORCA-IN 6 31610764 31610764 single base substitution G A downstream_gene_variant ORCA-IN 6 31610764 31610764 single base substitution G A exon_variant ORCA-IN 6 31610764 31610764 single base substitution G A intron_variant ORCA-IN 6 31610764 31610764 single base substitution G A stop_gained Q187* 559C>T ORCA-IN 6 31610764 31610764 single base substitution G A stop_gained Q593* 1777C>T ORCA-IN 6 31610764 31610764 single base substitution G A stop_gained Q599* 1795C>T ORCA-IN 6 31610764 31610764 single base substitution G A stop_gained Q629* 1885C>T ORCA-IN 6 31610764 31610764 single base substitution G A upstream_gene_variant OV-AU 6 31604503 31604503 single base substitution G C downstream_gene_variant OV-AU 6 31604556 31604556 single base substitution G C downstream_gene_variant OV-AU 6 31612738 31612738 single base substitution G C downstream_gene_variant OV-AU 6 31612738 31612738 single base substitution G C exon_variant OV-AU 6 31612738 31612738 single base substitution G C missense_variant H112D 334C>G OV-AU 6 31612738 31612738 single base substitution G C missense_variant H37D 109C>G OV-AU 6 31612738 31612738 single base substitution G C missense_variant H452D 1354C>G OV-AU 6 31612738 31612738 single base substitution G C missense_variant H458D 1372C>G OV-AU 6 31612738 31612738 single base substitution G C upstream_gene_variant OV-AU 6 31615645 31615645 single base substitution A C downstream_gene_variant OV-AU 6 31615645 31615645 single base substitution A C intron_variant OV-AU 6 31615645 31615645 single base substitution A C upstream_gene_variant OV-AU 6 31620447 31620447 single base substitution A T 5_prime_UTR_variant OV-AU 6 31620447 31620447 single base substitution A T upstream_gene_variant PACA-AU 6 31601992 31601992 single base substitution T C downstream_gene_variant PACA-AU 6 31603251 31603251 single base substitution G C downstream_gene_variant PACA-AU 6 31603589 31603589 single base substitution G A downstream_gene_variant PACA-AU 6 31606259 31606259 deletion of <=200bp T - downstream_gene_variant PACA-AU 6 31606560 31606560 single base substitution G A downstream_gene_variant PACA-AU 6 31606881 31606881 single base substitution G A 3_prime_UTR_variant PACA-AU 6 31606881 31606881 single base substitution G A downstream_gene_variant PACA-AU 6 31606881 31606881 single base substitution G A exon_variant PACA-AU 6 31606925 31606925 single base substitution A T downstream_gene_variant PACA-AU 6 31606925 31606925 single base substitution A T exon_variant PACA-AU 6 31606925 31606925 single base substitution A T missense_variant F1073I 3217T>A PACA-AU 6 31606925 31606925 single base substitution A T missense_variant F1122I 3364T>A PACA-AU 6 31606925 31606925 single base substitution A T missense_variant F1128I 3382T>A PACA-AU 6 31606925 31606925 single base substitution A T missense_variant F1158I 3472T>A PACA-AU 6 31606925 31606925 single base substitution A T missense_variant F131I 391T>A PACA-AU 6 31606925 31606925 single base substitution A T missense_variant F221I 661T>A PACA-AU 6 31606925 31606925 single base substitution A T missense_variant F899I 2695T>A PACA-AU 6 31606957 31606957 single base substitution C G downstream_gene_variant PACA-AU 6 31606957 31606957 single base substitution C G exon_variant PACA-AU 6 31606957 31606957 single base substitution C G missense_variant S1062T 3185G>C PACA-AU 6 31606957 31606957 single base substitution C G missense_variant S1111T 3332G>C PACA-AU 6 31606957 31606957 single base substitution C G missense_variant S1117T 3350G>C PACA-AU 6 31606957 31606957 single base substitution C G missense_variant S1147T 3440G>C PACA-AU 6 31606957 31606957 single base substitution C G missense_variant S120T 359G>C PACA-AU 6 31606957 31606957 single base substitution C G missense_variant S210T 629G>C PACA-AU 6 31606957 31606957 single base substitution C G missense_variant S888T 2663G>C PACA-AU 6 31607207 31607207 single base substitution G A downstream_gene_variant PACA-AU 6 31607207 31607207 single base substitution G A intron_variant PACA-AU 6 31608053 31608053 single base substitution G T downstream_gene_variant PACA-AU 6 31608053 31608053 single base substitution G T exon_variant PACA-AU 6 31608053 31608053 single base substitution G T missense_variant Q1021K 3061C>A PACA-AU 6 31608053 31608053 single base substitution G T missense_variant Q1027K 3079C>A PACA-AU 6 31608053 31608053 single base substitution G T missense_variant Q1057K 3169C>A PACA-AU 6 31608053 31608053 single base substitution G T missense_variant Q169K 505C>A PACA-AU 6 31608053 31608053 single base substitution G T missense_variant Q79K 235C>A PACA-AU 6 31608053 31608053 single base substitution G T missense_variant Q847K 2539C>A PACA-AU 6 31608053 31608053 single base substitution G T upstream_gene_variant PACA-AU 6 31610026 31610026 single base substitution G A downstream_gene_variant PACA-AU 6 31610026 31610026 single base substitution G A exon_variant PACA-AU 6 31610026 31610026 single base substitution G A missense_variant S571L 1712C>T PACA-AU 6 31610026 31610026 single base substitution G A missense_variant S697L 2090C>T PACA-AU 6 31610026 31610026 single base substitution G A missense_variant S703L 2108C>T PACA-AU 6 31610026 31610026 single base substitution G A missense_variant S733L 2198C>T PACA-AU 6 31610026 31610026 single base substitution G A upstream_gene_variant PACA-AU 6 31612796 31612796 single base substitution G A downstream_gene_variant PACA-AU 6 31612796 31612796 single base substitution G A exon_variant PACA-AU 6 31612796 31612796 single base substitution G A synonymous_variant T17T 51C>T PACA-AU 6 31612796 31612796 single base substitution G A synonymous_variant T432T 1296C>T PACA-AU 6 31612796 31612796 single base substitution G A synonymous_variant T438T 1314C>T PACA-AU 6 31612796 31612796 single base substitution G A synonymous_variant T92T 276C>T PACA-AU 6 31612796 31612796 single base substitution G A upstream_gene_variant PACA-AU 6 31612842 31612842 single base substitution G A downstream_gene_variant PACA-AU 6 31612842 31612842 single base substitution G A exon_variant PACA-AU 6 31612842 31612842 single base substitution G A missense_variant S2L 5C>T PACA-AU 6 31612842 31612842 single base substitution G A missense_variant S417L 1250C>T PACA-AU 6 31612842 31612842 single base substitution G A missense_variant S423L 1268C>T PACA-AU 6 31612842 31612842 single base substitution G A missense_variant S77L 230C>T PACA-AU 6 31612842 31612842 single base substitution G A upstream_gene_variant PACA-AU 6 31615010 31615010 single base substitution G A downstream_gene_variant PACA-AU 6 31615010 31615010 single base substitution G A intron_variant PACA-AU 6 31615010 31615010 single base substitution G A upstream_gene_variant PACA-AU 6 31617131 31617131 single base substitution G A missense_variant P90S 268C>T PACA-AU 6 31617131 31617131 single base substitution G A upstream_gene_variant PACA-AU 6 31617861 31617861 single base substitution G A intron_variant PACA-AU 6 31617861 31617861 single base substitution G A upstream_gene_variant PACA-AU 6 31623598 31623598 single base substitution G A upstream_gene_variant PAEN-AU 6 31612966 31612966 single base substitution C T downstream_gene_variant PAEN-AU 6 31612966 31612966 single base substitution C T exon_variant PAEN-AU 6 31612966 31612966 single base substitution C T missense_variant G36R 106G>A PAEN-AU 6 31612966 31612966 single base substitution C T missense_variant G376R 1126G>A PAEN-AU 6 31612966 31612966 single base substitution C T missense_variant G382R 1144G>A PAEN-AU 6 31612966 31612966 single base substitution C T upstream_gene_variant PAEN-AU 6 31618778 31618778 single base substitution G T intron_variant PBCA-DE 6 31607097 31607097 insertion of <=200bp - C downstream_gene_variant PBCA-DE 6 31607097 31607097 insertion of <=200bp - C intron_variant PBCA-DE 6 31611498 31611507 deletion of <=200bp CAAAAAAAAA - downstream_gene_variant PBCA-DE 6 31611498 31611507 deletion of <=200bp CAAAAAAAAA - intron_variant PBCA-DE 6 31611498 31611507 deletion of <=200bp CAAAAAAAAA - upstream_gene_variant PBCA-DE 6 31617340 31617340 single base substitution C T missense_variant R58Q 173G>A PBCA-DE 6 31617340 31617340 single base substitution C T upstream_gene_variant PBCA-DE 6 31622318 31622318 single base substitution C T upstream_gene_variant PRAD-UK 6 31616050 31616050 single base substitution C A downstream_gene_variant PRAD-UK 6 31616050 31616050 single base substitution C A intron_variant PRAD-UK 6 31616050 31616050 single base substitution C A upstream_gene_variant PRAD-UK 6 31623327 31623327 single base substitution G C upstream_gene_variant PRAD-UK 6 31623889 31623889 single base substitution G A upstream_gene_variant PRAD-US 6 31614196 31614196 single base substitution G A downstream_gene_variant PRAD-US 6 31614196 31614196 single base substitution G A missense_variant A298V 893C>T PRAD-US 6 31614196 31614196 single base substitution G A missense_variant A304V 911C>T PRAD-US 6 31614196 31614196 single base substitution G A upstream_gene_variant READ-US 6 31603457 31603457 single base substitution G A downstream_gene_variant RECA-EU 6 31610650 31610650 single base substitution G T downstream_gene_variant RECA-EU 6 31610650 31610650 single base substitution G T exon_variant RECA-EU 6 31610650 31610650 single base substitution G T intron_variant RECA-EU 6 31610650 31610650 single base substitution G T missense_variant P225T 673C>A RECA-EU 6 31610650 31610650 single base substitution G T missense_variant P631T 1891C>A RECA-EU 6 31610650 31610650 single base substitution G T missense_variant P637T 1909C>A RECA-EU 6 31610650 31610650 single base substitution G T missense_variant P667T 1999C>A RECA-EU 6 31610650 31610650 single base substitution G T upstream_gene_variant SKCA-BR 6 31602812 31602812 single base substitution C T downstream_gene_variant SKCA-BR 6 31603365 31603365 single base substitution C T downstream_gene_variant SKCA-BR 6 31606678 31606682 deletion of <=200bp AAAAC - downstream_gene_variant SKCA-BR 6 31607096 31607096 insertion of <=200bp - TC downstream_gene_variant SKCA-BR 6 31607096 31607096 insertion of <=200bp - TC intron_variant SKCA-BR 6 31614542 31614543 deletion of <=200bp TG - downstream_gene_variant SKCA-BR 6 31614542 31614543 deletion of <=200bp TG - intron_variant SKCA-BR 6 31614542 31614543 deletion of <=200bp TG - upstream_gene_variant SKCA-BR 6 31614543 31614543 single base substitution G T downstream_gene_variant SKCA-BR 6 31614543 31614543 single base substitution G T intron_variant SKCA-BR 6 31614543 31614543 single base substitution G T upstream_gene_variant SKCA-BR 6 31615235 31615235 single base substitution C T downstream_gene_variant SKCA-BR 6 31615235 31615235 single base substitution C T intron_variant SKCA-BR 6 31615235 31615235 single base substitution C T upstream_gene_variant SKCA-BR 6 31618757 31618759 deletion of <=200bp TTA - intron_variant SKCA-BR 6 31623322 31623322 single base substitution G A upstream_gene_variant SKCM-US 6 31602309 31602309 single base substitution C T downstream_gene_variant SKCM-US 6 31603361 31603361 single base substitution C T downstream_gene_variant SKCM-US 6 31603424 31603424 single base substitution C T downstream_gene_variant SKCM-US 6 31604046 31604046 single base substitution A G downstream_gene_variant SKCM-US 6 31604379 31604379 single base substitution C T downstream_gene_variant SKCM-US 6 31605326 31605326 single base substitution G A downstream_gene_variant SKCM-US 6 31606981 31606981 single base substitution C T downstream_gene_variant SKCM-US 6 31606981 31606981 single base substitution C T exon_variant SKCM-US 6 31606981 31606981 single base substitution C T missense_variant R1054Q 3161G>A SKCM-US 6 31606981 31606981 single base substitution C T missense_variant R1103Q 3308G>A SKCM-US 6 31606981 31606981 single base substitution C T missense_variant R1109Q 3326G>A SKCM-US 6 31606981 31606981 single base substitution C T missense_variant R112Q 335G>A SKCM-US 6 31606981 31606981 single base substitution C T missense_variant R1139Q 3416G>A SKCM-US 6 31606981 31606981 single base substitution C T missense_variant R202Q 605G>A SKCM-US 6 31606981 31606981 single base substitution C T missense_variant R880Q 2639G>A SKCM-US 6 31608000 31608000 single base substitution A G downstream_gene_variant SKCM-US 6 31608000 31608000 single base substitution A G exon_variant SKCM-US 6 31608000 31608000 single base substitution A G synonymous_variant S1038S 3114T>C SKCM-US 6 31608000 31608000 single base substitution A G synonymous_variant S1044S 3132T>C SKCM-US 6 31608000 31608000 single base substitution A G synonymous_variant S1074S 3222T>C SKCM-US 6 31608000 31608000 single base substitution A G synonymous_variant S186S 558T>C SKCM-US 6 31608000 31608000 single base substitution A G synonymous_variant S864S 2592T>C SKCM-US 6 31608000 31608000 single base substitution A G synonymous_variant S96S 288T>C SKCM-US 6 31608000 31608000 single base substitution A G upstream_gene_variant SKCM-US 6 31608042 31608042 single base substitution C T downstream_gene_variant SKCM-US 6 31608042 31608042 single base substitution C T exon_variant SKCM-US 6 31608042 31608042 single base substitution C T synonymous_variant R1024R 3072G>A SKCM-US 6 31608042 31608042 single base substitution C T synonymous_variant R1030R 3090G>A SKCM-US 6 31608042 31608042 single base substitution C T synonymous_variant R1060R 3180G>A SKCM-US 6 31608042 31608042 single base substitution C T synonymous_variant R172R 516G>A SKCM-US 6 31608042 31608042 single base substitution C T synonymous_variant R82R 246G>A SKCM-US 6 31608042 31608042 single base substitution C T synonymous_variant R850R 2550G>A SKCM-US 6 31608042 31608042 single base substitution C T upstream_gene_variant SKCM-US 6 31608608 31608608 single base substitution G A downstream_gene_variant SKCM-US 6 31608608 31608608 single base substitution G A exon_variant SKCM-US 6 31608608 31608608 single base substitution G A synonymous_variant A35A 105C>T SKCM-US 6 31608608 31608608 single base substitution G A synonymous_variant A77A 231C>T SKCM-US 6 31608608 31608608 single base substitution G A synonymous_variant A803A 2409C>T SKCM-US 6 31608608 31608608 single base substitution G A synonymous_variant A929A 2787C>T SKCM-US 6 31608608 31608608 single base substitution G A synonymous_variant A935A 2805C>T SKCM-US 6 31608608 31608608 single base substitution G A synonymous_variant A965A 2895C>T SKCM-US 6 31608608 31608608 single base substitution G A upstream_gene_variant SKCM-US 6 31609612 31609612 single base substitution G A downstream_gene_variant SKCM-US 6 31609612 31609612 single base substitution G A exon_variant SKCM-US 6 31609612 31609612 single base substitution G A stop_gained R654* 1960C>T SKCM-US 6 31609612 31609612 single base substitution G A stop_gained R780* 2338C>T SKCM-US 6 31609612 31609612 single base substitution G A stop_gained R786* 2356C>T SKCM-US 6 31609612 31609612 single base substitution G A stop_gained R816* 2446C>T SKCM-US 6 31609612 31609612 single base substitution G A upstream_gene_variant SKCM-US 6 31609699 31609699 single base substitution G A downstream_gene_variant SKCM-US 6 31609699 31609699 single base substitution G A exon_variant SKCM-US 6 31609699 31609699 single base substitution G A missense_variant L625F 1873C>T SKCM-US 6 31609699 31609699 single base substitution G A missense_variant L751F 2251C>T SKCM-US 6 31609699 31609699 single base substitution G A missense_variant L757F 2269C>T SKCM-US 6 31609699 31609699 single base substitution G A missense_variant L787F 2359C>T SKCM-US 6 31609699 31609699 single base substitution G A upstream_gene_variant SKCM-US 6 31610092 31610092 single base substitution G A downstream_gene_variant SKCM-US 6 31610092 31610092 single base substitution G A exon_variant SKCM-US 6 31610092 31610092 single base substitution G A intron_variant SKCM-US 6 31610092 31610092 single base substitution G A missense_variant P675L 2024C>T SKCM-US 6 31610092 31610092 single base substitution G A missense_variant P681L 2042C>T SKCM-US 6 31610092 31610092 single base substitution G A missense_variant P711L 2132C>T SKCM-US 6 31610092 31610092 single base substitution G A upstream_gene_variant SKCM-US 6 31610669 31610669 single base substitution G C downstream_gene_variant SKCM-US 6 31610669 31610669 single base substitution G C exon_variant SKCM-US 6 31610669 31610669 single base substitution G C intron_variant SKCM-US 6 31610669 31610669 single base substitution G C synonymous_variant P218P 654C>G SKCM-US 6 31610669 31610669 single base substitution G C synonymous_variant P624P 1872C>G SKCM-US 6 31610669 31610669 single base substitution G C synonymous_variant P630P 1890C>G SKCM-US 6 31610669 31610669 single base substitution G C synonymous_variant P660P 1980C>G SKCM-US 6 31610669 31610669 single base substitution G C upstream_gene_variant SKCM-US 6 31611729 31611729 single base substitution G T downstream_gene_variant SKCM-US 6 31611729 31611729 single base substitution G T exon_variant SKCM-US 6 31611729 31611729 single base substitution G T missense_variant A123D 368C>A SKCM-US 6 31611729 31611729 single base substitution G T missense_variant A163D 488C>A SKCM-US 6 31611729 31611729 single base substitution G T missense_variant A528D 1583C>A SKCM-US 6 31611729 31611729 single base substitution G T missense_variant A529D 1586C>A SKCM-US 6 31611729 31611729 single base substitution G T missense_variant A535D 1604C>A SKCM-US 6 31611729 31611729 single base substitution G T missense_variant A565D 1694C>A SKCM-US 6 31611729 31611729 single base substitution G T upstream_gene_variant SKCM-US 6 31611951 31611951 single base substitution G A downstream_gene_variant SKCM-US 6 31611951 31611951 single base substitution G A exon_variant SKCM-US 6 31611951 31611951 single base substitution G A intron_variant SKCM-US 6 31611951 31611951 single base substitution G A missense_variant P124S 370C>T SKCM-US 6 31611951 31611951 single base substitution G A missense_variant P490S 1468C>T SKCM-US 6 31611951 31611951 single base substitution G A missense_variant P496S 1486C>T SKCM-US 6 31611951 31611951 single base substitution G A missense_variant P526S 1576C>T SKCM-US 6 31611951 31611951 single base substitution G A missense_variant P84S 250C>T SKCM-US 6 31611951 31611951 single base substitution G A upstream_gene_variant SKCM-US 6 31612752 31612752 single base substitution G A downstream_gene_variant SKCM-US 6 31612752 31612752 single base substitution G A exon_variant SKCM-US 6 31612752 31612752 single base substitution G A missense_variant P107L 320C>T SKCM-US 6 31612752 31612752 single base substitution G A missense_variant P32L 95C>T SKCM-US 6 31612752 31612752 single base substitution G A missense_variant P447L 1340C>T SKCM-US 6 31612752 31612752 single base substitution G A missense_variant P453L 1358C>T SKCM-US 6 31612752 31612752 single base substitution G A upstream_gene_variant SKCM-US 6 31612874 31612874 single base substitution G A downstream_gene_variant SKCM-US 6 31612874 31612874 single base substitution G A exon_variant SKCM-US 6 31612874 31612874 single base substitution G A synonymous_variant S406S 1218C>T SKCM-US 6 31612874 31612874 single base substitution G A synonymous_variant S412S 1236C>T SKCM-US 6 31612874 31612874 single base substitution G A synonymous_variant S66S 198C>T SKCM-US 6 31612874 31612874 single base substitution G A upstream_gene_variant SKCM-US 6 31612884 31612884 single base substitution T C downstream_gene_variant SKCM-US 6 31612884 31612884 single base substitution T C exon_variant SKCM-US 6 31612884 31612884 single base substitution T C missense_variant Q403R 1208A>G SKCM-US 6 31612884 31612884 single base substitution T C missense_variant Q409R 1226A>G SKCM-US 6 31612884 31612884 single base substitution T C missense_variant Q63R 188A>G SKCM-US 6 31612884 31612884 single base substitution T C upstream_gene_variant SKCM-US 6 31615563 31615563 single base substitution G A downstream_gene_variant SKCM-US 6 31615563 31615563 single base substitution G A missense_variant P180L 539C>T SKCM-US 6 31615563 31615563 single base substitution G A missense_variant P198L 593C>T SKCM-US 6 31615563 31615563 single base substitution G A missense_variant P204L 611C>T SKCM-US 6 31615563 31615563 single base substitution G A upstream_gene_variant SKCM-US 6 31617056 31617056 single base substitution G A missense_variant P115S 343C>T SKCM-US 6 31617056 31617056 single base substitution G A upstream_gene_variant SKCM-US 6 31617103 31617103 single base substitution G T missense_variant S99Y 296C>A SKCM-US 6 31617103 31617103 single base substitution G T upstream_gene_variant SKCM-US 6 31623783 31623783 single base substitution G A upstream_gene_variant SKCM-US 6 31624370 31624370 single base substitution C A upstream_gene_variant SKCM-US 6 31625002 31625002 single base substitution G A upstream_gene_variant STAD-US 6 31602535 31602535 single base substitution T C downstream_gene_variant STAD-US 6 31602641 31602641 deletion of <=200bp C - downstream_gene_variant STAD-US 6 31602658 31602658 single base substitution A G downstream_gene_variant STAD-US 6 31602965 31602965 single base substitution G T downstream_gene_variant STAD-US 6 31603993 31603993 single base substitution C T downstream_gene_variant STAD-US 6 31604191 31604191 single base substitution C T downstream_gene_variant STAD-US 6 31604895 31604895 single base substitution G A downstream_gene_variant STAD-US 6 31605358 31605358 single base substitution C T downstream_gene_variant STAD-US 6 31608183 31608183 single base substitution A C downstream_gene_variant STAD-US 6 31608183 31608183 single base substitution A C exon_variant STAD-US 6 31608183 31608183 single base substitution A C intron_variant STAD-US 6 31608183 31608183 single base substitution A C synonymous_variant P1003P 3009T>G STAD-US 6 31608183 31608183 single base substitution A C synonymous_variant P1009P 3027T>G STAD-US 6 31608183 31608183 single base substitution A C synonymous_variant P1039P 3117T>G STAD-US 6 31608183 31608183 single base substitution A C synonymous_variant P151P 453T>G STAD-US 6 31608183 31608183 single base substitution A C upstream_gene_variant STAD-US 6 31608942 31608942 single base substitution A G downstream_gene_variant STAD-US 6 31608942 31608942 single base substitution A G exon_variant STAD-US 6 31608942 31608942 single base substitution A G missense_variant L21P 62T>C STAD-US 6 31608942 31608942 single base substitution A G missense_variant L747P 2240T>C STAD-US 6 31608942 31608942 single base substitution A G missense_variant L873P 2618T>C STAD-US 6 31608942 31608942 single base substitution A G missense_variant L879P 2636T>C STAD-US 6 31608942 31608942 single base substitution A G missense_variant L909P 2726T>C STAD-US 6 31608942 31608942 single base substitution A G upstream_gene_variant STAD-US 6 31609931 31609931 single base substitution C T downstream_gene_variant STAD-US 6 31609931 31609931 single base substitution C T exon_variant STAD-US 6 31609931 31609931 single base substitution C T missense_variant G603R 1807G>A STAD-US 6 31609931 31609931 single base substitution C T missense_variant G729R 2185G>A STAD-US 6 31609931 31609931 single base substitution C T missense_variant G735R 2203G>A STAD-US 6 31609931 31609931 single base substitution C T missense_variant G765R 2293G>A STAD-US 6 31609931 31609931 single base substitution C T upstream_gene_variant STAD-US 6 31610030 31610030 insertion of <=200bp - A downstream_gene_variant STAD-US 6 31610030 31610030 insertion of <=200bp - A exon_variant STAD-US 6 31610030 31610030 insertion of <=200bp - A frameshift_variant T570I? STAD-US 6 31610030 31610030 insertion of <=200bp - A frameshift_variant T696I? STAD-US 6 31610030 31610030 insertion of <=200bp - A frameshift_variant T702I? STAD-US 6 31610030 31610030 insertion of <=200bp - A frameshift_variant T732I? STAD-US 6 31610030 31610030 insertion of <=200bp - A upstream_gene_variant STAD-US 6 31611880 31611880 single base substitution C G downstream_gene_variant STAD-US 6 31611880 31611880 single base substitution C G exon_variant STAD-US 6 31611880 31611880 single base substitution C G intron_variant STAD-US 6 31611880 31611880 single base substitution C G synonymous_variant G107G 321G>C STAD-US 6 31611880 31611880 single base substitution C G synonymous_variant G147G 441G>C STAD-US 6 31611880 31611880 single base substitution C G synonymous_variant G513G 1539G>C STAD-US 6 31611880 31611880 single base substitution C G synonymous_variant G519G 1557G>C STAD-US 6 31611880 31611880 single base substitution C G synonymous_variant G549G 1647G>C STAD-US 6 31611880 31611880 single base substitution C G upstream_gene_variant STAD-US 6 31611972 31611972 single base substitution C A downstream_gene_variant STAD-US 6 31611972 31611972 single base substitution C A exon_variant STAD-US 6 31611972 31611972 single base substitution C A intron_variant STAD-US 6 31611972 31611972 single base substitution C A splice_acceptor_variant STAD-US 6 31611972 31611972 single base substitution C A upstream_gene_variant STAD-US 6 31612889 31612889 single base substitution A T downstream_gene_variant STAD-US 6 31612889 31612889 single base substitution A T exon_variant STAD-US 6 31612889 31612889 single base substitution A T synonymous_variant P401P 1203T>A STAD-US 6 31612889 31612889 single base substitution A T synonymous_variant P407P 1221T>A STAD-US 6 31612889 31612889 single base substitution A T synonymous_variant P61P 183T>A STAD-US 6 31612889 31612889 single base substitution A T upstream_gene_variant STAD-US 6 31614268 31614268 single base substitution A G downstream_gene_variant STAD-US 6 31614268 31614268 single base substitution A G missense_variant L274P 821T>C STAD-US 6 31614268 31614268 single base substitution A G missense_variant L280P 839T>C STAD-US 6 31614268 31614268 single base substitution A G upstream_gene_variant STAD-US 6 31615562 31615562 single base substitution C T downstream_gene_variant STAD-US 6 31615562 31615562 single base substitution C T synonymous_variant P180P 540G>A STAD-US 6 31615562 31615562 single base substitution C T synonymous_variant P198P 594G>A STAD-US 6 31615562 31615562 single base substitution C T synonymous_variant P204P 612G>A STAD-US 6 31615562 31615562 single base substitution C T upstream_gene_variant STAD-US 6 31619438 31619438 single base substitution C T missense_variant A35T 103G>A STAD-US 6 31624328 31624328 single base substitution C A upstream_gene_variant STAD-US 6 31625241 31625241 single base substitution G A upstream_gene_variant STAD-US 6 31625431 31625431 single base substitution G A upstream_gene_variant THCA-US 6 31602045 31602045 single base substitution C A downstream_gene_variant UCEC-US 6 31602684 31602684 single base substitution C A downstream_gene_variant UCEC-US 6 31604186 31604186 single base substitution C T downstream_gene_variant UCEC-US 6 31604302 31604302 single base substitution C T downstream_gene_variant UCEC-US 6 31607320 31607320 single base substitution C T downstream_gene_variant UCEC-US 6 31607320 31607320 single base substitution C T exon_variant UCEC-US 6 31607320 31607320 single base substitution C T intron_variant UCEC-US 6 31607320 31607320 single base substitution C T missense_variant R1081Q 3242G>A UCEC-US 6 31607320 31607320 single base substitution C T missense_variant R1087Q 3260G>A UCEC-US 6 31607320 31607320 single base substitution C T missense_variant R1117Q 3350G>A UCEC-US 6 31608030 31608030 single base substitution C T downstream_gene_variant UCEC-US 6 31608030 31608030 single base substitution C T exon_variant UCEC-US 6 31608030 31608030 single base substitution C T synonymous_variant P1028P 3084G>A UCEC-US 6 31608030 31608030 single base substitution C T synonymous_variant P1034P 3102G>A UCEC-US 6 31608030 31608030 single base substitution C T synonymous_variant P1064P 3192G>A UCEC-US 6 31608030 31608030 single base substitution C T synonymous_variant P176P 528G>A UCEC-US 6 31608030 31608030 single base substitution C T synonymous_variant P854P 2562G>A UCEC-US 6 31608030 31608030 single base substitution C T synonymous_variant P86P 258G>A UCEC-US 6 31608030 31608030 single base substitution C T upstream_gene_variant UCEC-US 6 31610082 31610082 single base substitution G A downstream_gene_variant UCEC-US 6 31610082 31610082 single base substitution G A exon_variant UCEC-US 6 31610082 31610082 single base substitution G A splice_region_variant UCEC-US 6 31610082 31610082 single base substitution G A synonymous_variant G678G 2034C>T UCEC-US 6 31610082 31610082 single base substitution G A synonymous_variant G684G 2052C>T UCEC-US 6 31610082 31610082 single base substitution G A synonymous_variant G714G 2142C>T UCEC-US 6 31610082 31610082 single base substitution G A upstream_gene_variant UCEC-US 6 31610655 31610655 single base substitution G A downstream_gene_variant UCEC-US 6 31610655 31610655 single base substitution G A exon_variant UCEC-US 6 31610655 31610655 single base substitution G A intron_variant UCEC-US 6 31610655 31610655 single base substitution G A missense_variant A223V 668C>T UCEC-US 6 31610655 31610655 single base substitution G A missense_variant A629V 1886C>T UCEC-US 6 31610655 31610655 single base substitution G A missense_variant A635V 1904C>T UCEC-US 6 31610655 31610655 single base substitution G A missense_variant A665V 1994C>T UCEC-US 6 31610655 31610655 single base substitution G A upstream_gene_variant UCEC-US 6 31611898 31611898 single base substitution C A downstream_gene_variant UCEC-US 6 31611898 31611898 single base substitution C A exon_variant UCEC-US 6 31611898 31611898 single base substitution C A intron_variant UCEC-US 6 31611898 31611898 single base substitution C A synonymous_variant R101R 303G>T UCEC-US 6 31611898 31611898 single base substitution C A synonymous_variant R141R 423G>T UCEC-US 6 31611898 31611898 single base substitution C A synonymous_variant R507R 1521G>T UCEC-US 6 31611898 31611898 single base substitution C A synonymous_variant R513R 1539G>T UCEC-US 6 31611898 31611898 single base substitution C A synonymous_variant R543R 1629G>T UCEC-US 6 31611898 31611898 single base substitution C A upstream_gene_variant UCEC-US 6 31612090 31612090 single base substitution C T downstream_gene_variant UCEC-US 6 31612090 31612090 single base substitution C T exon_variant UCEC-US 6 31612090 31612090 single base substitution C T intron_variant UCEC-US 6 31612090 31612090 single base substitution C T missense_variant A517T 1549G>A UCEC-US 6 31612090 31612090 single base substitution C T upstream_gene_variant UCEC-US 6 31612093 31612093 single base substitution C T downstream_gene_variant UCEC-US 6 31612093 31612093 single base substitution C T exon_variant UCEC-US 6 31612093 31612093 single base substitution C T intron_variant UCEC-US 6 31612093 31612093 single base substitution C T missense_variant A516T 1546G>A UCEC-US 6 31612093 31612093 single base substitution C T upstream_gene_variant UCEC-US 6 31617402 31617402 single base substitution C A missense_variant M37I 111G>T UCEC-US 6 31617402 31617402 single base substitution C A upstream_gene_variant UCEC-US 6 31624284 31624284 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ESCC_11 COSM4003939 c.500T>G p.V167G Substitution - Missense 6:31648729-31648729 - T3340 COSM4665038 c.477+1G>A p.? Unknown 6:31648910-31648910 - TCGA-D8-A1XK-01 COSM3830112 c.3006A>G p.E1002E Substitution - coding silent 6:31640409-31640409 - Pat_46_B COSM5870174 c.712C>T p.P238S Substitution - Missense 6:31647667-31647667 - J63_T COSM3948983 c.2274G>T p.M758I Substitution - Missense 6:31641899-31641899 - TCGA-D9-A6EC-06 COSM4401171 c.3114T>C p.S1038S Substitution - coding silent 6:31640223-31640223 - HCC113T COSM5808494 c.117A>G p.V39V Substitution - coding silent 6:31649619-31649619 - TCGA-EE-A2M5-06 COSM3624641 c.2787C>T p.A929A Substitution - coding silent 6:31640831-31640831 - Gp5D COSM3253647 c.2887C>T p.R963W Substitution - Missense 6:31640528-31640528 - TCGA-BR-6452-01 COSM3861748 c.1448-1G>T p.? Unknown 6:31644195-31644195 - 1257T COSM5762532 c.1126G>A p.G376R Substitution - Missense 6:31645189-31645189 - TCGA-DA-A1I5-06 COSM3624659 c.593C>T p.P198L Substitution - Missense 6:31647786-31647786 - RMS80_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - ESCC_120 COSM5640465 c.307G>A p.G103R Substitution - Missense 6:31649315-31649315 - PD24182a COSM5790833 c.1370-1G>C p.? Unknown 6:31644603-31644603 - TCGA-EE-A3AA-06 COSM3624653 c.1468C>T p.P490S Substitution - Missense 6:31644174-31644174 - T55 COSM4665032 c.1342G>A p.V448M Substitution - Missense 6:31644973-31644973 - SK01600_P COSM1600279 c.103G>A p.A35T Substitution - Missense 6:31651661-31651661 - HCC92 COSM1621431 c.1007A>T p.D336V Substitution - Missense 6:31645516-31645516 - TCGA-66-2780-01 COSM741904 c.2299G>T p.G767W Substitution - Missense 6:31641874-31641874 - PD3905a COSM3396780 c.325C>G p.H109D Substitution - Missense 6:31649297-31649297 - I2L-P19Ta-Tumor-Biopsy COSM3624657 c.1218C>T p.S406S Substitution - coding silent 6:31645097-31645097 - SNUH_G15_S1 COSM4003939 c.500T>G p.V167G Substitution - Missense 6:31648729-31648729 - TCGA-D1-A0ZS-01 COSM1077623 c.1886C>T p.A629V Substitution - Missense 6:31642878-31642878 - RMS105_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - ME002T COSM222095 c.469C>T p.P157S Substitution - Missense 6:31648919-31648919 - TCGA-BS-A0UF-01 COSM1077621 c.3084G>A p.P1028P Substitution - coding silent 6:31640253-31640253 - TCGA-D8-A27F-01 COSM1487604 c.1454A>G p.Q485R Substitution - Missense 6:31644188-31644188 - AOCS-137-3-7 COSM4153251 c.1354C>G p.H452D Substitution - Missense 6:31644961-31644961 - Pat_06_A COSM5870168 c.3029_3030insC p.E1011fs*24 Insertion - Frameshift 6:31640385-31640386 - BZ36 COSM5759206 c.2441G>A p.R814Q Substitution - Missense 6:31641549-31641549 - RMS88_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - S01453 COSM309433 c.588G>T p.P196P Substitution - coding silent 6:31647791-31647791 - SJHGG031_D COSM4970184 c.987C>T p.N329N Substitution - coding silent 6:31645536-31645536 - T3094 COSM309432 c.344delC p.P115fs*53 Deletion - Frameshift 6:31649278-31649278 - TCGA-D3-A2JO-06 COSM3624645 c.2251C>T p.L751F Substitution - Missense 6:31641922-31641922 - TCGA-EK-A2RA-01 COSM4848419 c.3289C>T p.R1097W Substitution - Missense 6:31639223-31639223 - RMS109_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - ICGC_MB81 COSM3765263 c.173G>A p.R58Q Substitution - Missense 6:31649563-31649563 - TCGA-BR-4362-01 COSM3861740 c.3009T>G p.P1003P Substitution - coding silent 6:31640406-31640406 - I2L-P19Ta-Tumor-Organoid COSM3624657 c.1218C>T p.S406S Substitution - coding silent 6:31645097-31645097 - T2384 COSM4665030 c.1398G>A p.P466P Substitution - coding silent 6:31644574-31644574 - TCGA-23-1027-01 COSM118124 c.3204C>T p.A1068A Substitution - coding silent 6:31639581-31639581 - T1760 COSM4665024 c.2156G>T p.S719I Substitution - Missense 6:31642183-31642183 - TCGA-FG-7637-01 COSM3928333 c.1239T>G p.N413K Substitution - Missense 6:31645076-31645076 - TCGA-CJ-4892-01 COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - PT36 COSM5915492 c.1282C>T p.P428S Substitution - Missense 6:31645033-31645033 - AOCS-137-1-X COSM4153251 c.1354C>G p.H452D Substitution - Missense 6:31644961-31644961 - TCGA-IR-A3LH-01 COSM4832665 c.2114C>T p.S705F Substitution - Missense 6:31642225-31642225 - RKO COSM3253675 c.2234T>C p.F745S Substitution - Missense 6:31641939-31641939 - T3021 COSM4665034 c.1287G>A p.P429P Substitution - coding silent 6:31645028-31645028 - CSCC-49-T COSM4531009 c.174G>A p.R58R Substitution - coding silent 6:31649562-31649562 - TCGA-EE-A20F-06 COSM3624647 c.2024C>T p.P675L Substitution - Missense 6:31642315-31642315 - LOVO COSM4614229 c.344_345insC p.G116fs*11 Insertion - Frameshift 6:31649277-31649278 - PT46 COSM3624655 c.1340C>T p.P447L Substitution - Missense 6:31644975-31644975 - TCGA-AA-3663-01 COSM1443308 c.2824delC p.Q942fs*85 Deletion - Frameshift 6:31640794-31640794 - TCGA-BR-A4QL-01 COSM1600279 c.103G>A p.A35T Substitution - Missense 6:31651661-31651661 - LS411 COSM3253754 c.614C>T p.P205L Substitution - Missense 6:31647765-31647765 - 2521259 COSM3624661 c.343C>T p.P115S Substitution - Missense 6:31649279-31649279 - TCGA-D9-A4Z5-01 COSM3624637 c.3308G>A p.R1103Q Substitution - Missense 6:31639204-31639204 - TCGA-A3-3374-01 COSM595959 c.1329G>A p.Q443Q Substitution - coding silent 6:31644986-31644986 - DN14065 COSM5962807 c.1741G>A p.A581T Substitution - Missense 6:31643023-31643023 - BK0050 COSM4187949 c.3179C>A p.A1060D Substitution - Missense 6:31639606-31639606 - 4_RESISTANT COSM1723860 c.2222_2223CC>TT p.A741V Substitution - Missense 6:31642116-31642117 - SNU-C4 COSM4654083 c.476A>C p.Q159P Substitution - Missense 6:31648912-31648912 - Gp2D COSM3253647 c.2887C>T p.R963W Substitution - Missense 6:31640528-31640528 - CT-TC COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - TCGA-DK-A1AB-01 COSM421404 c.399C>T p.V133V Substitution - coding silent 6:31649223-31649223 - 4_PRE-TREATMENT COSM1723860 c.2222_2223CC>TT p.A741V Substitution - Missense 6:31642116-31642117 - BN24T COSM1621429 c.1169delC p.P390fs*61 Deletion - Frameshift 6:31645146-31645146 - TCGA-BH-A0B1-01 COSM5835180 c.2127_2128insT p.L710fs*9 Insertion - Frameshift 6:31642211-31642212 - LUAD-S01315 COSM345827 c.1589C>T p.S530L Substitution - Missense 6:31643949-31643949 - HDC101 COSM4636131 c.3129G>A p.K1043K Substitution - coding silent 6:31640208-31640208 - PD6406a COSM5768892 c.922G>T p.E308* Substitution - Nonsense 6:31645601-31645601 - SNU-C1 COSM3253685 c.2100G>T p.Q700H Substitution - Missense 6:31642239-31642239 - SMS-CTR COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - SW48 COSM3253764 c.431G>A p.G144D Substitution - Missense 6:31648957-31648957 - TCGA-AX-A06H-01 COSM1077623 c.1886C>T p.A629V Substitution - Missense 6:31642878-31642878 - TCGA-AP-A051-01 COSM1077622 c.2034C>T p.G678G Substitution - coding silent 6:31642305-31642305 - CSCC-18-T COSM134119 c.421C>T p.P141S Substitution - Missense 6:31649201-31649201 - RMS85_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - T3080 COSM4665028 c.1521G>A p.R507R Substitution - coding silent 6:31644121-31644121 - Pat_01_B COSM5870170 c.1286delC p.P429fs*22 Deletion - Frameshift 6:31645029-31645029 - cSCCP1 COSM134119 c.421C>T p.P141S Substitution - Missense 6:31649201-31649201 - HCC098T COSM5806677 c.355G>T p.G119W Substitution - Missense 6:31649267-31649267 - TCGA-BT-A0YX-01 COSM421405 c.2418C>T p.I806I Substitution - coding silent 6:31641572-31641572 - B85-0-Tumor COSM4006353 c.2447G>A p.S816N Substitution - Missense 6:31641543-31641543 - TCGA-D5-6926-01 COSM1443307 c.2845A>G p.M949V Substitution - Missense 6:31640686-31640686 - TCGA-BS-A0UV-01 COSM1077624 c.1521G>T p.R507R Substitution - coding silent 6:31644121-31644121 - TCGA-AD-6964-01 COSM1443312 c.756C>T p.G252G Substitution - coding silent 6:31647623-31647623 - TCGA-BC-A217-01 COSM4936826 c.2994A>T p.S998S Substitution - coding silent 6:31640421-31640421 - C0059T COSM4155170 c.1891C>A p.P631T Substitution - Missense 6:31642873-31642873 - ICGC_0006 COSM218876 c.268C>T p.P90S Substitution - Missense 6:31649354-31649354 - CSCC-56-T COSM4565660 c.2349_2350CC>TT p.H784Y Substitution - Missense 6:31641823-31641824 - BZ30 COSM5758919 c.868C>T p.R290C Substitution - Missense 6:31646444-31646444 - 8047807 COSM3394090 c.1296C>T p.T432T Substitution - coding silent 6:31645019-31645019 - TCGA-BR-8679-01 COSM3861746 c.1539G>C p.G513G Substitution - coding silent 6:31644103-31644103 - TCGA-HU-A4GT-01 COSM3253756 c.594G>A p.P198P Substitution - coding silent 6:31647785-31647785 - TCGA-AA-A010-01 COSM279118 c.2642A>G p.Q881R Substitution - Missense 6:31641141-31641141 - TCGA-D3-A2JF-06 COSM3624639 c.3072G>A p.R1024R Substitution - coding silent 6:31640265-31640265 - TCGA-FS-A1ZK-06 COSM3624663 c.296C>A p.S99Y Substitution - Missense 6:31649326-31649326 - 326_PT COSM5756831 c.1482C>T p.T494T Substitution - coding silent 6:31644160-31644160 - TCGA-39-5016-01 COSM741905 c.2635G>T p.G879W Substitution - Missense 6:31641148-31641148 - PD3905a COSM3396780 c.325C>G p.H109D Substitution - Missense 6:31649297-31649297 - TCGA-D1-A174-01 COSM1077620 c.3242G>A p.R1081Q Substitution - Missense 6:31639543-31639543 - RMS106_ COSM4986451 c.724C>T p.P242S Substitution - Missense 6:31647655-31647655 - TCGA-G4-6302-01 COSM3697749 c.3105C>A p.A1035A Substitution - coding silent 6:31640232-31640232 - TCGA-BR-7707-01 COSM3861744 c.2185G>A p.G729R Substitution - Missense 6:31642154-31642154 - 326_CLM COSM5756831 c.1482C>T p.T494T Substitution - coding silent 6:31644160-31644160 - HCC26T COSM3662384 c.2871T>G p.A957A Substitution - coding silent 6:31640660-31640660 - MSK-PCa6_organoid COSM5423833 c.2720G>C p.W907S Substitution - Missense 6:31640898-31640898 - TCGA-HF-7133-01 COSM3861752 c.821T>C p.L274P Substitution - Missense 6:31646491-31646491 - ESO-152 COSM1245988 c.553-10C>T p.? Unknown 6:31647836-31647836 - I2L-P10-Tumor-Organoid COSM5357147 c.904G>A p.D302N Substitution - Missense 6:31646408-31646408 - tumor_4119027 COSM5946334 c.1936-13_1936-10delCTTT p.? Unknown 6:31642413-31642416 - TCGA-ER-A19H-06 COSM3624655 c.1340C>T p.P447L Substitution - Missense 6:31644975-31644975 - TCGA-DD-A4NB-01 COSM4940833 c.1658C>T p.T553I Substitution - Missense 6:31643106-31643106 - 8031121 COSM3394084 c.3364T>A p.F1122I Substitution - Missense 6:31639148-31639148 - CRC-06T COSM5457252 c.3190G>A p.A1064T Substitution - Missense 6:31639595-31639595 - TCGA-D9-A6EC-06 COSM4405049 c.1208A>G p.Q403R Substitution - Missense 6:31645107-31645107 - TCGA-DA-A1I4-06 COSM3624651 c.1586C>A p.A529D Substitution - Missense 6:31643952-31643952 - LOVO COSM1443311 c.1169_1170insC p.T391fs*29 Insertion - Frameshift 6:31645145-31645146 - CSCC-56-T COSM4460894 c.1165C>T p.P389S Substitution - Missense 6:31645150-31645150 - HCC1395 COSM32743 c.3381+3C>G p.? Unknown 6:31639128-31639128 - 8031121 COSM3394086 c.3061C>A p.Q1021K Substitution - Missense 6:31640276-31640276 - T1154 COSM4665026 c.1533T>G p.P511P Substitution - coding silent 6:31644109-31644109 - TCGA-CJ-4918-01 COSM483865 c.1520G>T p.R507L Substitution - Missense 6:31644122-31644122 - SC_9094 COSM1443309 c.1953T>C p.P651P Substitution - coding silent 6:31642386-31642386 - CSCC-5-T COSM4449419 c.2228-1G>A p.? Unknown 6:31641946-31641946 - T3182 COSM4665022 c.2176C>T p.R726C Substitution - Missense 6:31642163-31642163 - TCGA-39-5031-01 COSM741906 c.3229G>A p.E1077K Substitution - Missense 6:31639556-31639556 - TCGA-HU-A4GT-01 COSM3861742 c.2618T>C p.L873P Substitution - Missense 6:31641165-31641165 - LUAD-RT-S01774 COSM381580 c.1570G>T p.G524C Substitution - Missense 6:31643968-31643968 - T3340 COSM4665040 c.459G>A p.M153I Substitution - Missense 6:31648929-31648929 - ATL075 COSM5710058 c.146C>T p.S49F Substitution - Missense 6:31649590-31649590 - S00827 COSM309431 c.595C>T p.Q199* Substitution - Nonsense 6:31647784-31647784 - TCGA-BS-A0UF-01 COSM1077625 c.111G>T p.M37I Substitution - Missense 6:31649625-31649625 - Pat_53_B COSM1443308 c.2824delC p.Q942fs*85 Deletion - Frameshift 6:31640794-31640794 - 59 COSM5014578 c.797C>G p.S266C Substitution - Missense 6:31646515-31646515 - TCGA-BP-4349-01 COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - LIM1899 COSM3253701 c.1590G>A p.S530S Substitution - coding silent 6:31643948-31643948 - T2269 COSM4665043 c.275C>G p.T92S Substitution - Missense 6:31649347-31649347 - S02234 COSM5676254 c.1193C>T p.P398L Substitution - Missense 6:31645122-31645122 - 2171670 COSM4423264 c.1415C>A p.P472H Substitution - Missense 6:31644557-31644557 - LN18 COSM3253738 c.844A>T p.S282C Substitution - Missense 6:31646468-31646468 - PTC-73C COSM4160842 c.1569C>T p.A523A Substitution - coding silent 6:31643969-31643969 - 8031121 COSM218876 c.268C>T p.P90S Substitution - Missense 6:31649354-31649354 - 8031121 COSM218875 c.1250C>T p.S417L Substitution - Missense 6:31645065-31645065 - OSCC-GB_00160111 COSM3715468 c.1777C>T p.Q593* Substitution - Nonsense 6:31642987-31642987 - T3174 COSM4665036 c.1039C>T p.R347* Substitution - Nonsense 6:31645484-31645484 - 1115156 COSM5566353 c.1499G>A p.R500Q Substitution - Missense 6:31644143-31644143 - HCC039T COSM5809421 c.1631T>C p.M544T Substitution - Missense 6:31643907-31643907 - ICGC_0006 COSM218875 c.1250C>T p.S417L Substitution - Missense 6:31645065-31645065 - ccRCC-66 COSM1659926 c.2241C>G p.A747A Substitution - coding silent 6:31641932-31641932 - sysucc-1171T COSM5447891 c.813C>T p.V271V Substitution - coding silent 6:31646499-31646499 - Pat_53_A COSM309432 c.344delC p.P115fs*53 Deletion - Frameshift 6:31649278-31649278 - TCGA-G4-6293-01 COSM1443310 c.1243G>A p.E415K Substitution - Missense 6:31645072-31645072 - T3049 COSM1443308 c.2824delC p.Q942fs*85 Deletion - Frameshift 6:31640794-31640794 - S01453 COSM309433 c.588G>T p.P196P Substitution - coding silent 6:31647791-31647791 - RMS112_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - LS411 COSM3253669 c.2460G>A p.V820V Substitution - coding silent 6:31641414-31641414 - S02248 COSM5679797 c.1959A>C p.P653P Substitution - coding silent 6:31642380-31642380 - BD57T COSM5510140 c.1179T>C p.N393N Substitution - coding silent 6:31645136-31645136 - RH30SJ_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - TCGA-HC-7752-01 COSM3674656 c.893C>T p.A298V Substitution - Missense 6:31646419-31646419 - TCGA-CK-5916-01 COSM1443313 c.103delG p.A35fs*3 Deletion - Frameshift 6:31651661-31651661 - LUAD_E00522 COSM353435 c.903G>T p.T301T Substitution - coding silent 6:31646409-31646409 - 8069453 COSM3784511 c.3332G>C p.S1111T Substitution - Missense 6:31639180-31639180 - RMS10_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - I2L-P19Ta-Tumor-Organoid COSM5357292 c.2966G>A p.G989D Substitution - Missense 6:31640449-31640449 - sysucc-882T COSM5447700 c.379C>T p.R127W Substitution - Missense 6:31649243-31649243 - TCGA-EE-A2GE-06 COSM3624643 c.2338C>T p.R780* Substitution - Nonsense 6:31641835-31641835 - HCT15 COSM3253728 c.1109C>A p.P370H Substitution - Missense 6:31645414-31645414 - T8 COSM5345134 c.674G>A p.R225Q Substitution - Missense 6:31647705-31647705 - HCC92T COSM1621431 c.1007A>T p.D336V Substitution - Missense 6:31645516-31645516 - PD22355a COSM5771052 c.2405C>G p.T802S Substitution - Missense 6:31641585-31641585 - TCGA-A4-A5DU-01 COSM3994836 c.1371T>A p.D457E Substitution - Missense 6:31644601-31644601 - Pat_41_B COSM5870176 c.622G>A p.V208I Substitution - Missense 6:31647757-31647757 - Pat_01_B COSM5870172 c.1189C>T p.P397S Substitution - Missense 6:31645126-31645126 - 8031121 COSM3394088 c.2090C>T p.S697L Substitution - Missense 6:31642249-31642249 - SCMC_RM2_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - SK01600_M COSM1600279 c.103G>A p.A35T Substitution - Missense 6:31651661-31651661 - Pat_01_A COSM5870172 c.1189C>T p.P397S Substitution - Missense 6:31645126-31645126 - 16T COSM3715468 c.1777C>T p.Q593* Substitution - Nonsense 6:31642987-31642987 - ccRCC-7 COSM1665365 c.779delA p.N260fs*57 Deletion - Frameshift 6:31647600-31647600 - SNUH_G57_S1 COSM3684217 c.194T>G p.V65G Substitution - Missense 6:31649542-31649542 - T3094 COSM4665015 c.2910T>C p.P970P Substitution - coding silent 6:31640505-31640505 - cSCCP2 COSM137451 c.1225C>T p.P409S Substitution - Missense 6:31645090-31645090 - TCGA-CC-A7IJ-01 COSM4924499 c.2979A>G p.E993E Substitution - coding silent 6:31640436-31640436 - T2269 COSM4665018 c.2424G>A p.G808G Substitution - coding silent 6:31641566-31641566 - T3498 COSM309432 c.344delC p.P115fs*53 Deletion - Frameshift 6:31649278-31649278 - TCGA-B0-5098-01 COSM1496295 c.751G>A p.A251T Substitution - Missense 6:31647628-31647628 - T3024 COSM1621429 c.1169delC p.P390fs*61 Deletion - Frameshift 6:31645146-31645146 - 8 COSM5014580 c.139G>C p.A47P Substitution - Missense 6:31649597-31649597 - TCGA-A3-3346-01 COSM1496296 c.1161G>C p.R387R Substitution - coding silent 6:31645154-31645154 - TCGA-CC-A3MB-01 COSM4933806 c.2044C>T p.P682S Substitution - Missense 6:31642295-31642295 - TCGA-25-1633-01 COSM82018 c.903G>A p.T301T Substitution - coding silent 6:31646409-31646409 - TCGA-EE-A2GC-06 COSM3624657 c.1218C>T p.S406S Substitution - coding silent 6:31645097-31645097 - SS6003306 COSM5951077 c.172C>T p.R58W Substitution - Missense 6:31649564-31649564 - RMS111_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - T2197 COSM4665020 c.2420C>T p.T807M Substitution - Missense 6:31641570-31641570 - RMS110_ COSM3774230 c.1855T>C p.S619P Substitution - Missense 6:31642909-31642909 - CRC-02T COSM5455478 c.505G>A p.A169T Substitution - Missense 6:31648724-31648724 - TCGA-EE-A3AA-06 COSM3624661 c.343C>T p.P115S Substitution - Missense 6:31649279-31649279 - CSCC-62-T COSM4459458 c.1108C>T p.P370S Substitution - Missense 6:31645415-31645415 - I2L-P19Ta-Tumor-Biopsy COSM5357292 c.2966G>A p.G989D Substitution - Missense 6:31640449-31640449 - S00827 COSM309431 c.595C>T p.Q199* Substitution - Nonsense 6:31647784-31647784 - TCGA-FP-A4BE-01 COSM3861750 c.1203T>A p.P401P Substitution - coding silent 6:31645112-31645112 - PT16_1 COSM5898292 c.2228-5C>T p.? Unknown 6:31641950-31641950 - HCC159T COSM5806677 c.355G>T p.G119W Substitution - Missense 6:31649267-31649267 - LUAD-S01302 COSM396195 c.929G>T p.R310L Substitution - Missense 6:31645594-31645594 - HCC26 COSM3662384 c.2871T>G p.A957A Substitution - coding silent 6:31640660-31640660 - S00936 COSM309432 c.344delC p.P115fs*53 Deletion - Frameshift 6:31649278-31649278 - CSCC-56-T COSM4564844 c.1481_1482CC>TT p.T494I Substitution - Missense 6:31644160-31644161 - TCGA-ER-A19J-06 COSM3624649 c.1872C>G p.P624P Substitution - coding silent 6:31642892-31642892 - T3152 COSM1443308 c.2824delC p.Q942fs*85 Deletion - Frameshift 6:31640794-31640794 - TCGA-KR-A7K8-01 COSM4918204 c.1998G>T p.Q666H Substitution - Missense 6:31642341-31642341 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.440900 6p21.3 142590

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.N419K c.1257T>G 6 31612853 LGG - A Frameshift p.M602Ifs*3 c.1805dupT 6 31610754 HNSC - A Frameshift p.T702Yfs*23 c.2103dupT 6 31610031 STAD A G Missense p.M172T c.515T>C 6 31616491 LUAD C A Missense p.G773W c.2317G>T 6 31609651 LUSC C A Missense p.G885W c.2653G>T 6 31608925 LUSC C A Missense p.R1087L c.3260G>T 6 31607320 CM C A Missense p.R163L c.488G>T 6 31616518 CM C A Missense p.R174M c.521G>T 6 31616485 STAD C A Missense p.R513L c.1538G>T 6 31611899 RCCC C A Nonsense p.E1112* c.3334G>T 6 31606973 STAD C A Synonymous p.L333L c.999G>T 6 31613319 CM C A Synonymous p.P202P c.606G>T 6 31615568 SCLC CC AA Missense p.G103W c.306_307delinsTT 6 31617092 CM CC AA Missense p.G382* c.1143_1144delinsTT 6 31612966 CM CC AA Missense p.G612W c.1833_1834delinsTT 6 31610725 CM CC AA SpliceAcceptorBlockSubstitution . c.2906_2907delinsTT 6 31608303 CM C G 3-UTRSNV . c.3396+6C>G 6 31606905 BRCA CG AT Missense p.R182M c.544_545delinsAT 6 31616461 CM CG AT Missense p.R231M c.691_692delinsAT 6 31615482 CM CG AT Missense p.R997M c.2989_2990delinsAT 6 31608220 CM C G IntronicSNV . c.1465+12G>C 6 31612290 STAD C G SpliceAcceptorSNV . c.227-1G>C 6 31617173 STAD C G Synonymous p.R393R c.1179G>C 6 31612931 LGG C T IntronicSNV . c.1466-119G>A 6 31612090 UCEC C T IntronicSNV . c.1466-122G>A 6 31612093 UCEC C T IntronicSNV . c.2698-41G>A 6 31608756 CM C T Missense p.E1083K c.3247G>A 6 31607333 LUSC C T Missense p.E1112K c.3334G>A 6 31606973 HNSC C T Missense p.R1087Q c.3260G>A 6 31607320 UCEC C T Missense p.R58Q c.173G>A 6 31617340 MB C T Synonymous p.P565P c.1695G>A 6 31610864 CM C T Synonymous p.Q449Q c.1347G>A 6 31612763 LUAD C T Synonymous p.R1030R c.3090G>A 6 31608042 CM C T Synonymous p.T307T c.921G>A 6 31614186 OV G A Missense p.A304V c.911C>T 6 31614196 PRAD G A Missense p.A635V c.1904C>T 6 31610655 UCEC G A Missense p.H363Y c.1087C>T 6 31613231 CM G A Missense p.L757F c.2269C>T 6 31609699 CM G A Missense p.P115S c.343C>T 6 31617056 CM G A Missense p.P157S c.469C>T 6 31616696 CM G A Missense p.P204L c.611C>T 6 31615563 CM G A Missense p.P207L c.620C>T 6 31615554 CM G A Missense p.P252S c.754C>T 6 31615420 CM G A Missense p.P453L c.1358C>T 6 31612752 CM G A Missense p.P496S c.1486C>T 6 31611951 CM G A Missense p.P681L c.2042C>T 6 31610092 CM G A Missense p.P90S c.268C>T 6 31617131 PAAD G A Missense p.P992S c.2974C>T 6 31608236 CM G A Missense p.S423L c.1268C>T 6 31612842 PAAD G A Nonsense p.Q205* c.613C>T 6 31615561 SCLC G A Nonsense p.R786* c.2356C>T 6 31609612 CM G A Synonymous p.A1074A c.3222C>T 6 31607358 OV G A Synonymous p.A935A c.2805C>T 6 31608608 CM G A Synonymous p.I812I c.2436C>T 6 31609349 BLCA G A Synonymous p.P187P c.561C>T 6 31615613 ESCA G A Synonymous p.S412S c.1236C>T 6 31612874 CM G A Synonymous p.V133V c.399C>T 6 31617000 BLCA G C Missense p.R182G c.544C>G 6 31616462 CM G C Missense p.S412C c.1235C>G 6 31612875 LUAD G C Synonymous p.L290L c.870C>G 6 31614237 LUAD G C Synonymous p.P630P c.1890C>G 6 31610669 CM G - Frameshift p.P115Lfs*53 c.344delC 6 31617055 SCLC - G Frameshift p.Q776Pfs*28 c.2326dupC 6 31609642 RCCC GG AA Missense p.R1087W c.3258_3259delinsTT 6 31607321 CM G T Missense p.A535D c.1604C>A 6 31611729 CM G T Missense p.P141H c.422C>A 6 31616977 LUAD G T Missense p.S99Y c.296C>A 6 31617103 CM G T Synonymous p.P586P c.1758C>A 6 31610801 COREAD T A Missense p.E237D c.711A>T 6 31615463 HNSC T C Missense p.Q491R c.1472A>G 6 31611965 BRCA