Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 17 7094036 7094036 + Missense_Mutation SNP C C G TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr17:7094036C>G c.2166G>C c.(2164-2166)gaG>gaC p.E722D BLCA 17 7094102 7094102 + Silent SNP G G T TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr17:7094102G>T c.2100C>A c.(2098-2100)atC>atA p.I700I BLCA 17 7094110 7094110 + Missense_Mutation SNP C C T TCGA-CF-A3MI-01A-11D-A20D-08 TCGA-CF-A3MI-10A-01D-A20D-08 g.chr17:7094110C>T c.2092G>A c.(2092-2094)Gag>Aag p.E698K BLCA 17 7096312 7096312 + Silent SNP G G A TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr17:7096312G>A c.1818C>T c.(1816-1818)agC>agT p.S606S BLCA 17 7096379 7096379 + Missense_Mutation SNP G G A TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr17:7096379G>A c.1751C>T c.(1750-1752)tCg>tTg p.S584L BLCA 17 7099849 7099849 + Missense_Mutation SNP T T G TCGA-FD-A5BZ-01A-11D-A289-08 TCGA-FD-A5BZ-10A-01D-A289-08 g.chr17:7099849T>G c.1129A>C c.(1129-1131)Att>Ctt p.I377L BLCA 17 7107013 7107013 + Silent SNP G G A TCGA-ZF-AA54-01A-11D-A391-08 TCGA-ZF-AA54-10A-01D-A394-08 g.chr17:7107013G>A c.333C>T c.(331-333)ctC>ctT p.L111L BLCA 17 7121570 7121570 + 5'Flank SNP G G C TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr17:7121570G>C BLCA 17 7121592 7121592 + 5'Flank SNP C C A TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr17:7121592C>A BRCA 17 7096884 7096884 + Silent SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr17:7096884G>A c.1611C>T c.(1609-1611)atC>atT p.I537I BRCA 17 7100285 7100285 + Missense_Mutation SNP G G A TCGA-E2-A1IN-01A-11D-A13L-09 TCGA-E2-A1IN-10A-01D-A188-09 g.chr17:7100285G>A c.874C>T c.(874-876)Cgg>Tgg p.R292W CESC 17 7097021 7097021 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr17:7097021G>C c.1556C>G c.(1555-1557)tCg>tGg p.S519W CESC 17 7099654 7099654 + Splice_Site SNP C C G TCGA-DS-A0VM-01A-11D-A10S-08 TCGA-DS-A0VM-10A-01D-A10S-08 g.chr17:7099654C>G c.e11-1 COAD 17 7094077 7094077 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr17:7094077C>T c.2125G>A c.(2125-2127)Gag>Aag p.E709K COAD 17 7094130 7094130 + Missense_Mutation SNP A A G TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr17:7094130A>G c.2072T>C c.(2071-2073)aTc>aCc p.I691T COAD 17 7095237 7095237 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:7095237G>A c.1951C>T c.(1951-1953)Cgc>Tgc p.R651C COAD 17 7096397 7096397 + Missense_Mutation SNP C C T TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr17:7096397C>T c.1733G>A c.(1732-1734)cGg>cAg p.R578Q COAD 17 7096822 7096822 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr17:7096822T>C c.1673A>G c.(1672-1674)aAg>aGg p.K558R COAD 17 7099862 7099862 + Silent SNP A A G TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr17:7099862A>G c.1116T>C c.(1114-1116)caT>caC p.H372H COAD 17 7100221 7100221 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr17:7100221C>T c.938G>A c.(937-939)cGa>cAa p.R313Q COAD 17 7106631 7106631 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr17:7106631C>T c.523G>A c.(523-525)Gca>Aca p.A175T COAD 17 7107036 7107036 + Missense_Mutation SNP C C A TCGA-F4-6807-01A-11D-1835-10 TCGA-F4-6807-10A-01D-1835-10 g.chr17:7107036C>A c.310G>T c.(310-312)Gct>Tct p.A104S COAD 17 7107052 7107052 + Missense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr17:7107052C>A c.294G>T c.(292-294)aaG>aaT p.K98N COAD 17 7107081 7107081 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr17:7107081C>T c.265G>A c.(265-267)Ggt>Agt p.G89S COAD 17 7111526 7111526 + Silent SNP A A G TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr17:7111526A>G c.63T>C c.(61-63)ccT>ccC p.P21P COAD 17 7111526 7111526 + Silent SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr17:7111526A>G c.63T>C c.(61-63)ccT>ccC p.P21P COAD 17 7111532 7111532 + Silent SNP C C T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr17:7111532C>T c.57G>A c.(55-57)acG>acA p.T19T COAD 17 7121904 7121904 + 5'Flank DEL G G - TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr17:7121904delG COADREAD 17 7094077 7094077 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr17:7094077C>T c.2125G>A c.(2125-2127)Gag>Aag p.E709K COADREAD 17 7094130 7094130 + Missense_Mutation SNP A A G TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr17:7094130A>G c.2072T>C c.(2071-2073)aTc>aCc p.I691T COADREAD 17 7095237 7095237 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:7095237G>A c.1951C>T c.(1951-1953)Cgc>Tgc p.R651C COADREAD 17 7096397 7096397 + Missense_Mutation SNP C C T TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr17:7096397C>T c.1733G>A c.(1732-1734)cGg>cAg p.R578Q COADREAD 17 7096822 7096822 + Missense_Mutation SNP T T C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr17:7096822T>C c.1673A>G c.(1672-1674)aAg>aGg p.K558R COADREAD 17 7096856 7096856 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:7096856C>T c.1639G>A c.(1639-1641)Gcc>Acc p.A547T COADREAD 17 7099862 7099862 + Silent SNP A A G TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr17:7099862A>G c.1116T>C c.(1114-1116)caT>caC p.H372H COADREAD 17 7100221 7100221 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr17:7100221C>T c.938G>A c.(937-939)cGa>cAa p.R313Q COADREAD 17 7106631 7106631 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr17:7106631C>T c.523G>A c.(523-525)Gca>Aca p.A175T COADREAD 17 7107036 7107036 + Missense_Mutation SNP C C A TCGA-F4-6807-01A-11D-1835-10 TCGA-F4-6807-10A-01D-1835-10 g.chr17:7107036C>A c.310G>T c.(310-312)Gct>Tct p.A104S COADREAD 17 7107052 7107052 + Missense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr17:7107052C>A c.294G>T c.(292-294)aaG>aaT p.K98N COADREAD 17 7107081 7107081 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr17:7107081C>T c.265G>A c.(265-267)Ggt>Agt p.G89S COADREAD 17 7111526 7111526 + Silent SNP A A G TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr17:7111526A>G c.63T>C c.(61-63)ccT>ccC p.P21P COADREAD 17 7111526 7111526 + Silent SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr17:7111526A>G c.63T>C c.(61-63)ccT>ccC p.P21P COADREAD 17 7111532 7111532 + Silent SNP C C T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr17:7111532C>T c.57G>A c.(55-57)acG>acA p.T19T COADREAD 17 7121904 7121904 + 5'Flank DEL G G - TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr17:7121904delG ESCA 17 7095249 7095249 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr17:7095249C>T c.1939G>A c.(1939-1941)Gcc>Acc p.A647T ESCA 17 7096810 7096810 + Missense_Mutation SNP C C A TCGA-LN-A9FP-01A-31D-A387-09 TCGA-LN-A9FP-10A-01D-A38A-09 g.chr17:7096810C>A c.1685G>T c.(1684-1686)tGt>tTt p.C562F ESCA 17 7099575 7099575 + Missense_Mutation SNP G G A TCGA-L5-A4OU-01A-11D-A28B-09 TCGA-L5-A4OU-11A-11D-A28E-09 g.chr17:7099575G>A c.1265C>T c.(1264-1266)tCc>tTc p.S422F ESCA 17 7106648 7106648 + Splice_Site SNP C C T TCGA-L5-A88T-01A-11D-A351-09 TCGA-L5-A88T-11A-11D-A351-09 g.chr17:7106648C>T c.506G>A c.(505-507)gGt>gAt p.G169D GBM 17 7097030 7097030 + Missense_Mutation SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr17:7097030C>T c.1547G>A c.(1546-1548)cGa>cAa p.R516Q GBM 17 7099833 7099833 + Missense_Mutation SNP G G A TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr17:7099833G>A c.1145C>T c.(1144-1146)gCg>gTg p.A382V GBM 17 7121951 7121951 + 5'Flank SNP C C G TCGA-02-2470-01A-01D-1494-08 TCGA-02-2470-10A-01D-1494-08 g.chr17:7121951C>G GBMLGG 17 7094074 7094074 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7094074C>T c.2128G>A c.(2128-2130)Gac>Aac p.D710N GBMLGG 17 7097030 7097030 + Missense_Mutation SNP C C T TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr17:7097030C>T c.1547G>A c.(1546-1548)cGa>cAa p.R516Q GBMLGG 17 7099810 7099810 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7099810C>T c.1168G>A c.(1168-1170)Gct>Act p.A390T GBMLGG 17 7099833 7099833 + Missense_Mutation SNP G G A TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr17:7099833G>A c.1145C>T c.(1144-1146)gCg>gTg p.A382V GBMLGG 17 7100196 7100196 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7100196C>T c.963G>A c.(961-963)acG>acA p.T321T GBMLGG 17 7106755 7106755 + Missense_Mutation SNP T T G TCGA-FG-6688-01A-11D-1893-08 TCGA-FG-6688-10A-01D-1893-08 g.chr17:7106755T>G c.493A>C c.(493-495)Aag>Cag p.K165Q GBMLGG 17 7121951 7121951 + 5'Flank SNP C C G TCGA-02-2470-01A-01D-1494-08 TCGA-02-2470-10A-01D-1494-08 g.chr17:7121951C>G HNSC 17 7096290 7096290 + Nonsense_Mutation SNP G G A TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr17:7096290G>A c.1840C>T c.(1840-1842)Cag>Tag p.Q614* HNSC 17 7099547 7099547 + Silent SNP G G A TCGA-BA-5151-01A-01D-1434-08 TCGA-BA-5151-10A-01D-1434-08 g.chr17:7099547G>A c.1293C>T c.(1291-1293)ttC>ttT p.F431F HNSC 17 7099579 7099579 + Missense_Mutation SNP C C A TCGA-UF-A7JJ-01A-11D-A34J-08 TCGA-UF-A7JJ-10A-01D-A34M-08 g.chr17:7099579C>A c.1261G>T c.(1261-1263)Gcg>Tcg p.A421S HNSC 17 7111543 7111543 + Missense_Mutation SNP C C G TCGA-CV-A45P-01A-11D-A24D-08 TCGA-CV-A45P-10A-01D-A24F-08 g.chr17:7111543C>G c.46G>C c.(46-48)Gat>Cat p.D16H KIPAN 17 7106870 7106870 + Silent SNP G G A TCGA-IA-A83S-01A-11D-A34Z-10 TCGA-IA-A83S-11A-11D-A34Z-10 g.chr17:7106870G>A c.378C>T c.(376-378)cgC>cgT p.R126R KIPAN 17 7111517 7111517 + Missense_Mutation SNP G G T TCGA-B0-5400-01A-01D-1501-10 TCGA-B0-5400-11A-01D-1501-10 g.chr17:7111517G>T c.72C>A c.(70-72)caC>caA p.H24Q KIRC 17 7111517 7111517 + Missense_Mutation SNP G G T TCGA-B0-5400-01A-01D-1501-10 TCGA-B0-5400-11A-01D-1501-10 g.chr17:7111517G>T c.72C>A c.(70-72)caC>caA p.H24Q KIRP 17 7106870 7106870 + Silent SNP G G A TCGA-IA-A83S-01A-11D-A34Z-10 TCGA-IA-A83S-11A-11D-A34Z-10 g.chr17:7106870G>A c.378C>T c.(376-378)cgC>cgT p.R126R LGG 17 7094074 7094074 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7094074C>T c.2128G>A c.(2128-2130)Gac>Aac p.D710N LGG 17 7099810 7099810 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7099810C>T c.1168G>A c.(1168-1170)Gct>Act p.A390T LGG 17 7100196 7100196 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:7100196C>T c.963G>A c.(961-963)acG>acA p.T321T LGG 17 7106755 7106755 + Missense_Mutation SNP T T G TCGA-FG-6688-01A-11D-1893-08 TCGA-FG-6688-10A-01D-1893-08 g.chr17:7106755T>G c.493A>C c.(493-495)Aag>Cag p.K165Q LIHC 17 7097797 7097797 + Missense_Mutation SNP T T C TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr17:7097797T>C c.1319A>G c.(1318-1320)gAc>gGc p.D440G LIHC 17 7097812 7097812 + Missense_Mutation SNP G G A TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr17:7097812G>A c.1304C>T c.(1303-1305)gCc>gTc p.A435V LIHC 17 7097812 7097812 + Missense_Mutation SNP G G A TCGA-EP-A12J-01A-11D-A12Z-10 TCGA-EP-A12J-10A-01D-A12Z-10 g.chr17:7097812G>A c.1304C>T c.(1303-1305)gCc>gTc p.A435V LIHC 17 7106632 7106632 + Silent SNP G G A TCGA-DD-AAD2-01A-11D-A40R-10 TCGA-DD-AAD2-10A-01D-A40U-10 g.chr17:7106632G>A c.522C>T c.(520-522)atC>atT p.I174I LUAD 17 7094030 7094030 + Silent SNP G G C TCGA-91-6830-01A-11D-1945-08 TCGA-91-6830-11A-01D-1945-08 g.chr17:7094030G>C c.2172C>G c.(2170-2172)ctC>ctG p.L724L LUAD 17 7095232 7095232 + Silent SNP G G A TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr17:7095232G>A c.1956C>T c.(1954-1956)ccC>ccT p.P652P LUAD 17 7095235 7095235 + Silent SNP G G C TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr17:7095235G>C c.1953C>G c.(1951-1953)cgC>cgG p.R651R LUAD 17 7096430 7096430 + Missense_Mutation SNP G G T TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr17:7096430G>T c.1700C>A c.(1699-1701)aCa>aAa p.T567K LUAD 17 7097767 7097767 + Missense_Mutation SNP T T A TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr17:7097767T>A c.1349A>T c.(1348-1350)cAg>cTg p.Q450L LUAD 17 7097798 7097798 + Missense_Mutation SNP C C T TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chr17:7097798C>T c.1318G>A c.(1318-1320)Gac>Aac p.D440N LUAD 17 7100242 7100242 + Missense_Mutation SNP T T A TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr17:7100242T>A c.917A>T c.(916-918)gAc>gTc p.D306V LUAD 17 7107081 7107081 + Missense_Mutation SNP C C T TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr17:7107081C>T c.265G>A c.(265-267)Ggt>Agt p.G89S LUAD 17 7107104 7107104 + Missense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr17:7107104C>A c.242G>T c.(241-243)gGt>gTt p.G81V LUAD 17 7107105 7107105 + Missense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr17:7107105C>A c.241G>T c.(241-243)Ggt>Tgt p.G81C LUAD 17 7107548 7107548 + Silent SNP G G A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr17:7107548G>A c.120C>T c.(118-120)gtC>gtT p.V40V LUSC 17 7094078 7094078 + Silent SNP G G A TCGA-18-3407-01A-01D-0983-08 TCGA-18-3407-11A-01D-0983-08 g.chr17:7094078G>A c.2124C>T c.(2122-2124)atC>atT p.I708I LUSC 17 7095304 7095304 + Silent SNP G G A TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr17:7095304G>A c.1884C>T c.(1882-1884)ctC>ctT p.L628L LUSC 17 7097029 7097029 + Silent SNP T T A TCGA-43-5668-01A-01D-1632-08 TCGA-43-5668-11A-01D-1632-08 g.chr17:7097029T>A c.1548A>T c.(1546-1548)cgA>cgT p.R516R LUSC 17 7100162 7100162 + Missense_Mutation SNP C C G TCGA-21-5787-01A-01D-1632-08 TCGA-21-5787-10A-01D-1632-08 g.chr17:7100162C>G c.997G>C c.(997-999)Ggt>Cgt p.G333R OV 17 7100125 7100125 + Missense_Mutation SNP C C T TCGA-59-2352-01A-01W-0799-08 TCGA-59-2352-10A-01W-0800-08 g.chr17:7100125C>T c.1034G>A c.(1033-1035)gGc>gAc p.G345D PAAD 17 7099798 7099798 + Missense_Mutation SNP G G C TCGA-2J-AAB8-01A-12D-A40W-08 TCGA-2J-AAB8-10A-01D-A40W-08 g.chr17:7099798G>C c.1180C>G c.(1180-1182)Cca>Gca p.P394A PAAD 17 7100076 7100076 + Splice_Site SNP C C T TCGA-2J-AAB4-01A-12D-A40W-08 TCGA-2J-AAB4-10A-01D-A40W-08 g.chr17:7100076C>T c.1083G>A c.(1081-1083)tcG>tcA p.S361S PAAD 17 7106591 7106591 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:7106591C>A c.563G>T c.(562-564)aGc>aTc p.S188I PRAD 17 7096281 7096281 + Nonsense_Mutation SNP G G A TCGA-ZG-A9LZ-01A-11D-A41K-08 TCGA-ZG-A9LZ-10A-01D-A41N-08 g.chr17:7096281G>A c.1849C>T c.(1849-1851)Cga>Tga p.R617* PRAD 17 7096378 7096378 + Silent SNP C C T TCGA-HC-7213-01A-11D-2114-08 TCGA-HC-7213-10A-01D-2115-08 g.chr17:7096378C>T c.1752G>A c.(1750-1752)tcG>tcA p.S584S PRAD 17 7097030 7097030 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:7097030C>T c.1547G>A c.(1546-1548)cGa>cAa p.R516Q PRAD 17 7100327 7100327 + Missense_Mutation SNP G G T TCGA-EJ-A7NH-01A-12D-A33T-08 TCGA-EJ-A7NH-10A-01D-A33W-08 g.chr17:7100327G>T c.832C>A c.(832-834)Ctg>Atg p.L278M READ 17 7096856 7096856 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:7096856C>T c.1639G>A c.(1639-1641)Gcc>Acc p.A547T SARC 17 7094060 7094060 + Silent SNP G G A TCGA-QQ-A5V9-01A-11D-A32I-09 TCGA-QQ-A5V9-11A-31D-A32I-09 g.chr17:7094060G>A c.2142C>T c.(2140-2142)ccC>ccT p.P714P SKCM 17 7095232 7095232 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr17:7095232G>A c.1956C>T c.(1954-1956)ccC>ccT p.P652P SKCM 17 7095233 7095233 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr17:7095233G>A c.1955C>T c.(1954-1956)cCc>cTc p.P652L SKCM 17 7095250 7095250 + Silent SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr17:7095250G>A c.1938C>T c.(1936-1938)atC>atT p.I646I SKCM 17 7095250 7095250 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr17:7095250G>A c.1938C>T c.(1936-1938)atC>atT p.I646I SKCM 17 7096426 7096426 + Silent SNP C C T TCGA-D3-A1Q4-06A-11D-A196-08 TCGA-D3-A1Q4-10A-01D-A198-08 g.chr17:7096426C>T c.1704G>A c.(1702-1704)cgG>cgA p.R568R SKCM 17 7096904 7096917 + Splice_Site DEL CTGCAGAGAGAGCC CTGCAGAGAGAGCC - TCGA-FS-A1YX-06A-11D-A197-08 TCGA-FS-A1YX-10A-01D-A199-08 g.chr17:7096904_7096917delCTGCAGAGAGAGCC c.e16-1 SKCM 17 7097293 7097293 + Nonsense_Mutation SNP A A C TCGA-FW-A3TV-06A-11D-A23B-08 TCGA-FW-A3TV-10A-01D-A23B-08 g.chr17:7097293A>C c.1505T>G c.(1504-1506)tTa>tGa p.L502* SKCM 17 7100082 7100082 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr17:7100082G>A c.1077C>T c.(1075-1077)atC>atT p.I359I SKCM 17 7100290 7100290 + Missense_Mutation SNP G G A TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr17:7100290G>A c.869C>T c.(868-870)tCc>tTc p.S290F SKCM 17 7106564 7106564 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr17:7106564C>T c.590G>A c.(589-591)gGg>gAg p.G197E SKCM 17 7106568 7106568 + Missense_Mutation SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr17:7106568C>T c.586G>A c.(586-588)Gaa>Aaa p.E196K SKCM 17 7107049 7107049 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr17:7107049G>A c.297C>T c.(295-297)atC>atT p.I99I SKCM 17 7111499 7111499 + Silent SNP G G A TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr17:7111499G>A c.90C>T c.(88-90)ccC>ccT p.P30P BLCA 17 18133326 18133326 + Silent SNP C C T TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr17:18133326C>T c.153C>T c.(151-153)atC>atT p.I51I BLCA 17 18135878 18135878 + Silent SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr17:18135878C>T c.249C>T c.(247-249)ttC>ttT p.F83F BLCA 17 18137636 18137636 + Missense_Mutation SNP C C T TCGA-CF-A3MG-01A-11D-A20D-08 TCGA-CF-A3MG-10A-01D-A20D-08 g.chr17:18137636C>T c.764C>T c.(763-765)tCa>tTa p.S255L BLCA 17 18141407 18141407 + Missense_Mutation SNP T T A TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr17:18141407T>A c.1931T>A c.(1930-1932)cTg>cAg p.L644Q BLCA 17 18145214 18145214 + Missense_Mutation SNP C C T TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr17:18145214C>T c.2783C>T c.(2782-2784)tCc>tTc p.S928F BLCA 17 18145297 18145297 + Missense_Mutation SNP G G A TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr17:18145297G>A c.2866G>A c.(2866-2868)Gat>Aat p.D956N BRCA 17 18138574 18138574 + Missense_Mutation SNP G G A TCGA-A7-A5ZV-01A-11D-A28B-09 TCGA-A7-A5ZV-10A-01D-A28E-09 g.chr17:18138574G>A c.1232G>A c.(1231-1233)cGc>cAc p.R411H BRCA 17 18140040 18140042 + In_Frame_Del DEL AGG AGG - TCGA-A8-A07E-01A-11W-A050-09 TCGA-A8-A07E-10A-01W-A055-09 g.chr17:18140040_18140042delAGG c.1472_1474delAGG c.(1471-1476)caggct>cct p.491_492QA>P BRCA 17 18140048 18140050 + In_Frame_Del DEL GAG GAG - TCGA-A8-A07E-01A-11W-A050-09 TCGA-A8-A07E-10A-01W-A055-09 g.chr17:18140048_18140050delGAG c.1480_1482delGAG c.(1480-1482)gagdel p.E494del BRCA 17 18145296 18145296 + Silent SNP C C T TCGA-AR-A1AU-01A-11D-A12Q-09 TCGA-AR-A1AU-10A-01D-A12Q-09 g.chr17:18145296C>T c.2865C>T c.(2863-2865)cgC>cgT p.R955R BRCA 17 18145941 18145941 + Splice_Site SNP G G C TCGA-C8-A12U-01A-11D-A10Y-09 TCGA-C8-A12U-10A-01D-A110-09 g.chr17:18145941G>C c.3115G>C c.(3115-3117)Ggc>Cgc p.G1039R CESC 17 18138202 18138202 + Missense_Mutation SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr17:18138202G>A c.955G>A c.(955-957)Gac>Aac p.D319N CESC 17 18141887 18141887 + Missense_Mutation SNP C C T TCGA-DG-A2KL-01A-11D-A17W-09 TCGA-DG-A2KL-10A-01D-A17W-09 g.chr17:18141887C>T c.2170C>T c.(2170-2172)Cgt>Tgt p.R724C COAD 17 18135989 18135989 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr17:18135989C>T c.265C>T c.(265-267)Cgc>Tgc p.R89C COAD 17 18138227 18138227 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:18138227G>A c.980G>A c.(979-981)cGa>cAa p.R327Q COAD 17 18138798 18138799 + Frame_Shift_Ins INS - - G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr17:18138798_18138799insG c.1299_1300insG c.(1300-1302)gggfs p.G434fs COAD 17 18140207 18140207 + Missense_Mutation SNP T T C TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:18140207T>C c.1565T>C c.(1564-1566)cTc>cCc p.L522P COAD 17 18144014 18144014 + Missense_Mutation SNP G G A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr17:18144014G>A c.2329G>A c.(2329-2331)Gtg>Atg p.V777M COAD 17 18144975 18144975 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr17:18144975C>T c.2713C>T c.(2713-2715)Cgg>Tgg p.R905W COAD 17 18145296 18145296 + Silent SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr17:18145296C>T c.2865C>T c.(2863-2865)cgC>cgT p.R955R COADREAD 17 18135989 18135989 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr17:18135989C>T c.265C>T c.(265-267)Cgc>Tgc p.R89C COADREAD 17 18137141 18137141 + Missense_Mutation SNP A A G TCGA-AG-3885-01A-01W-0899-10 TCGA-AG-3885-10A-01W-0901-10 g.chr17:18137141A>G c.442A>G c.(442-444)Agc>Ggc p.S148G COADREAD 17 18138227 18138227 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:18138227G>A c.980G>A c.(979-981)cGa>cAa p.R327Q COADREAD 17 18138798 18138799 + Frame_Shift_Ins INS - - G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr17:18138798_18138799insG c.1299_1300insG c.(1300-1302)gggfs p.G434fs COADREAD 17 18140207 18140207 + Missense_Mutation SNP T T C TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr17:18140207T>C c.1565T>C c.(1564-1566)cTc>cCc p.L522P COADREAD 17 18144014 18144014 + Missense_Mutation SNP G G A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr17:18144014G>A c.2329G>A c.(2329-2331)Gtg>Atg p.V777M COADREAD 17 18144975 18144975 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr17:18144975C>T c.2713C>T c.(2713-2715)Cgg>Tgg p.R905W COADREAD 17 18145296 18145296 + Silent SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr17:18145296C>T c.2865C>T c.(2863-2865)cgC>cgT p.R955R ESCA 17 18133339 18133339 + Missense_Mutation SNP G G A TCGA-LN-A4MR-01A-11D-A28B-09 TCGA-LN-A4MR-10A-01D-A28E-09 g.chr17:18133339G>A c.166G>A c.(166-168)Ggg>Agg p.G56R ESCA 17 18137690 18137690 + Missense_Mutation SNP C C T TCGA-R6-A8W8-01B-11D-A37C-09 TCGA-R6-A8W8-10A-01D-A37F-09 g.chr17:18137690C>T c.818C>T c.(817-819)aCg>aTg p.T273M ESCA 17 18137986 18137986 + Missense_Mutation SNP A A G TCGA-VR-A8Q7-01A-11D-A37C-09 TCGA-VR-A8Q7-10A-01D-A37F-09 g.chr17:18137986A>G c.874A>G c.(874-876)Aac>Gac p.N292D ESCA 17 18138543 18138543 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr17:18138543G>A c.1201G>A c.(1201-1203)Gtg>Atg p.V401M GBM 17 18135847 18135847 + Missense_Mutation SNP G G A TCGA-06-6694-01A-12D-1845-08 TCGA-06-6694-10A-01D-1845-08 g.chr17:18135847G>A c.218G>A c.(217-219)cGg>cAg p.R73Q GBM 17 18138556 18138556 + Missense_Mutation SNP C C G TCGA-19-2631-01A-01D-1353-08 TCGA-19-2631-10B-01D-1353-08 g.chr17:18138556C>G c.1214C>G c.(1213-1215)cCc>cGc p.P405R GBMLGG 17 18135847 18135847 + Missense_Mutation SNP G G A TCGA-06-6694-01A-12D-1845-08 TCGA-06-6694-10A-01D-1845-08 g.chr17:18135847G>A c.218G>A c.(217-219)cGg>cAg p.R73Q GBMLGG 17 18138556 18138556 + Missense_Mutation SNP C C G TCGA-19-2631-01A-01D-1353-08 TCGA-19-2631-10B-01D-1353-08 g.chr17:18138556C>G c.1214C>G c.(1213-1215)cCc>cGc p.P405R GBMLGG 17 18140194 18140194 + Nonsense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:18140194C>T c.1552C>T c.(1552-1554)Cag>Tag p.Q518* GBMLGG 17 18145015 18145015 + Missense_Mutation SNP C C T TCGA-DU-8167-01A-11D-2253-08 TCGA-DU-8167-10A-01D-2253-08 g.chr17:18145015C>T c.2753C>T c.(2752-2754)aCg>aTg p.T918M GBMLGG 17 18145559 18145559 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:18145559G>A c.2962G>A c.(2962-2964)Gga>Aga p.G988R HNSC 17 18137344 18137344 + Missense_Mutation SNP G G A TCGA-MT-A67G-01A-11D-A30E-08 TCGA-MT-A67G-10A-01D-A30H-08 g.chr17:18137344G>A c.569G>A c.(568-570)cGc>cAc p.R190H HNSC 17 18144788 18144788 + Silent SNP C C T TCGA-CR-7373-01A-11D-2012-08 TCGA-CR-7373-10A-01D-2013-08 g.chr17:18144788C>T c.2526C>T c.(2524-2526)agC>agT p.S842S HNSC 17 18145527 18145527 + Missense_Mutation SNP C C T TCGA-CQ-A4CI-01A-11D-A25Y-08 TCGA-CQ-A4CI-10A-01D-A25Y-08 g.chr17:18145527C>T c.2930C>T c.(2929-2931)cCa>cTa p.P977L KIPAN 17 18135884 18135884 + Silent SNP C C T TCGA-CJ-6033-01A-11D-1669-08 TCGA-CJ-6033-11A-01D-1669-08 g.chr17:18135884C>T c.255C>T c.(253-255)acC>acT p.T85T KIPAN 17 18136083 18136083 + Missense_Mutation SNP A A G TCGA-CZ-4857-01A-01D-1373-10 TCGA-CZ-4857-11A-01D-1373-10 g.chr17:18136083A>G c.359A>G c.(358-360)cAg>cGg p.Q120R KIPAN 17 18137219 18137219 + Missense_Mutation SNP C C G TCGA-J7-A8I2-01A-12D-A35Z-10 TCGA-J7-A8I2-10A-01D-A35Z-10 g.chr17:18137219C>G c.520C>G c.(520-522)Cag>Gag p.Q174E KIPAN 17 18137246 18137246 + Missense_Mutation SNP C C T TCGA-B0-5081-01A-01D-1462-08 TCGA-B0-5081-11A-01D-1462-08 g.chr17:18137246C>T c.547C>T c.(547-549)Cgc>Tgc p.R183C KIPAN 17 18141525 18141526 + Frame_Shift_Ins INS - - A TCGA-A3-3358-01A-01D-1534-10 TCGA-A3-3358-11A-01D-1534-10 g.chr17:18141525_18141526insA c.2049_2050insA c.(2050-2052)aagfs p.K684fs KIPAN 17 18144992 18144992 + Silent SNP C C T TCGA-B8-5162-01A-01D-1421-08 TCGA-B8-5162-10A-01D-1421-08 g.chr17:18144992C>T c.2730C>T c.(2728-2730)agC>agT p.S910S KIRC 17 18135884 18135884 + Silent SNP C C T TCGA-CJ-6033-01A-11D-1669-08 TCGA-CJ-6033-11A-01D-1669-08 g.chr17:18135884C>T c.255C>T c.(253-255)acC>acT p.T85T KIRC 17 18136083 18136083 + Missense_Mutation SNP A A G TCGA-CZ-4857-01A-01D-1373-10 TCGA-CZ-4857-11A-01D-1373-10 g.chr17:18136083A>G c.359A>G c.(358-360)cAg>cGg p.Q120R KIRC 17 18137246 18137246 + Missense_Mutation SNP C C T TCGA-B0-5081-01A-01D-1462-08 TCGA-B0-5081-11A-01D-1462-08 g.chr17:18137246C>T c.547C>T c.(547-549)Cgc>Tgc p.R183C KIRC 17 18141525 18141526 + Frame_Shift_Ins INS - - A TCGA-A3-3358-01A-01D-1534-10 TCGA-A3-3358-11A-01D-1534-10 g.chr17:18141525_18141526insA c.2049_2050insA c.(2050-2052)aagfs p.K684fs KIRC 17 18144992 18144992 + Silent SNP C C T TCGA-B8-5162-01A-01D-1421-08 TCGA-B8-5162-10A-01D-1421-08 g.chr17:18144992C>T c.2730C>T c.(2728-2730)agC>agT p.S910S KIRP 17 18137219 18137219 + Missense_Mutation SNP C C G TCGA-J7-A8I2-01A-12D-A35Z-10 TCGA-J7-A8I2-10A-01D-A35Z-10 g.chr17:18137219C>G c.520C>G c.(520-522)Cag>Gag p.Q174E LGG 17 18140194 18140194 + Nonsense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:18140194C>T c.1552C>T c.(1552-1554)Cag>Tag p.Q518* LGG 17 18145015 18145015 + Missense_Mutation SNP C C T TCGA-DU-8167-01A-11D-2253-08 TCGA-DU-8167-10A-01D-2253-08 g.chr17:18145015C>T c.2753C>T c.(2752-2754)aCg>aTg p.T918M LGG 17 18145559 18145559 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:18145559G>A c.2962G>A c.(2962-2964)Gga>Aga p.G988R LIHC 17 18138832 18138832 + Nonsense_Mutation SNP C C T TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr17:18138832C>T c.1333C>T c.(1333-1335)Cga>Tga p.R445* LUAD 17 18133340 18133340 + Missense_Mutation SNP G G T TCGA-05-4420-01A-01D-1265-08 TCGA-05-4420-10A-01D-1265-08 g.chr17:18133340G>T c.167G>T c.(166-168)gGg>gTg p.G56V LUAD 17 18135839 18135839 + Silent SNP C C T TCGA-44-7659-01A-11D-2063-08 TCGA-44-7659-10A-01D-2063-08 g.chr17:18135839C>T c.210C>T c.(208-210)ggC>ggT p.G70G LUAD 17 18137461 18137461 + Missense_Mutation SNP G G A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr17:18137461G>A c.686G>A c.(685-687)tGt>tAt p.C229Y LUAD 17 18138158 18138158 + Missense_Mutation SNP A A G TCGA-91-6830-01A-11D-1945-08 TCGA-91-6830-11A-01D-1945-08 g.chr17:18138158A>G c.911A>G c.(910-912)cAc>cGc p.H304R LUAD 17 18138449 18138449 + Silent SNP G G T TCGA-78-7146-01A-11D-2036-08 TCGA-78-7146-10A-01D-2036-08 g.chr17:18138449G>T c.1107G>T c.(1105-1107)ctG>ctT p.L369L LUAD 17 18139956 18139956 + Missense_Mutation SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr17:18139956C>T c.1388C>T c.(1387-1389)tCg>tTg p.S463L LUAD 17 18141033 18141033 + Missense_Mutation SNP C C G TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr17:18141033C>G c.1850C>G c.(1849-1851)aCc>aGc p.T617S LUAD 17 18141833 18141833 + Missense_Mutation SNP G G T TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr17:18141833G>T c.2116G>T c.(2116-2118)Gtg>Ttg p.V706L LUAD 17 18145251 18145251 + Silent SNP G G C TCGA-75-5146-01A-01D-1625-08 TCGA-75-5146-10A-01D-1625-08 g.chr17:18145251G>C c.2820G>C c.(2818-2820)cgG>cgC p.R940R LUSC 17 18136004 18136004 + Missense_Mutation SNP C C A TCGA-21-5784-01A-01D-1632-08 TCGA-21-5784-10A-01D-1632-08 g.chr17:18136004C>A c.280C>A c.(280-282)Ctt>Att p.L94I OV 17 18138572 18138572 + Silent SNP C C A TCGA-29-2427-01A-01W-0799-08 TCGA-29-2427-10A-01W-0800-08 g.chr17:18138572C>A c.1230C>A c.(1228-1230)gcC>gcA p.A410A OV 17 18139976 18139976 + Missense_Mutation SNP C C T TCGA-29-2429-01A-01D-1526-09 TCGA-29-2429-10A-01D-1526-09 g.chr17:18139976C>T c.1408C>T c.(1408-1410)Ctc>Ttc p.L470F OV 17 18141444 18141444 + Silent SNP C C T TCGA-20-1682-01A-01W-0633-09 TCGA-20-1682-10A-01W-0633-09 g.chr17:18141444C>T c.1968C>T c.(1966-1968)ctC>ctT p.L656L PAAD 17 18133300 18133300 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:18133300G>A c.127G>A c.(127-129)Gac>Aac p.D43N PAAD 17 18135840 18135840 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:18135840C>T c.211C>T c.(211-213)Ctg>Ttg p.L71L PAAD 17 18138215 18138215 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:18138215T>C c.968T>C c.(967-969)gTa>gCa p.V323A PAAD 17 18138848 18138848 + Missense_Mutation SNP C C T TCGA-FB-A5VM-01A-11D-A32N-08 TCGA-FB-A5VM-10A-01D-A32N-08 g.chr17:18138848C>T c.1349C>T c.(1348-1350)aCg>aTg p.T450M PAAD 17 18141066 18141066 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:18141066G>A c.1883G>A c.(1882-1884)cGc>cAc p.R628H PAAD 17 18144854 18144854 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:18144854G>A c.2592G>A c.(2590-2592)acG>acA p.T864T PAAD 17 18145222 18145222 + Nonsense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:18145222G>T c.2791G>T c.(2791-2793)Gaa>Taa p.E931* PCPG 17 18138460 18138460 + Missense_Mutation SNP A A G TCGA-WB-A81P-01A-11D-A35I-08 TCGA-WB-A81P-10A-01D-A35G-08 g.chr17:18138460A>G c.1118A>G c.(1117-1119)gAc>gGc p.D373G PRAD 17 18137336 18137336 + Silent SNP C C T TCGA-CH-5738-01A-11D-1576-08 TCGA-CH-5738-10A-01D-1576-08 g.chr17:18137336C>T c.561C>T c.(559-561)gaC>gaT p.D187D PRAD 17 18137432 18137432 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:18137432G>A c.657G>A c.(655-657)ctG>ctA p.L219L PRAD 17 18138412 18138413 + Frame_Shift_Ins INS - - C TCGA-V1-A8MU-01A-11D-A377-08 TCGA-V1-A8MU-10A-01D-A37A-08 g.chr17:18138412_18138413insC c.1070_1071insC c.(1069-1074)gaccccfs p.DP357fs PRAD 17 18139975 18139975 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:18139975G>A c.1407G>A c.(1405-1407)ccG>ccA p.P469P PRAD 17 18141473 18141473 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:18141473G>A c.1997G>A c.(1996-1998)cGc>cAc p.R666H PRAD 17 18141892 18141892 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:18141892C>T c.2175C>T c.(2173-2175)tgC>tgT p.C725C PRAD 17 18144821 18144821 + Missense_Mutation SNP G G T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:18144821G>T c.2559G>T c.(2557-2559)gaG>gaT p.E853D READ 17 18137141 18137141 + Missense_Mutation SNP A A G TCGA-AG-3885-01A-01W-0899-10 TCGA-AG-3885-10A-01W-0901-10 g.chr17:18137141A>G c.442A>G c.(442-444)Agc>Ggc p.S148G SKCM 17 18137373 18137373 + Missense_Mutation SNP T T G TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr17:18137373T>G c.598T>G c.(598-600)Tca>Gca p.S200A SKCM 17 18137691 18137691 + Silent SNP G G A TCGA-D3-A3C3-06A-12D-A19A-08 TCGA-D3-A3C3-10A-01D-A19A-08 g.chr17:18137691G>A c.819G>A c.(817-819)acG>acA p.T273T SKCM 17 18138301 18138301 + Missense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr17:18138301G>A c.1054G>A c.(1054-1056)Gag>Aag p.E352K SKCM 17 18138461 18138461 + Silent SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr17:18138461C>T c.1119C>T c.(1117-1119)gaC>gaT p.D373D SKCM 17 18138462 18138462 + Silent SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr17:18138462C>T c.1120C>T c.(1120-1122)Ctg>Ttg p.L374L SKCM 17 18138547 18138547 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr17:18138547C>T c.1205C>T c.(1204-1206)gCc>gTc p.A402V SKCM 17 18139963 18139963 + Silent SNP G G A TCGA-FS-A1ZS-06A-12D-A197-08 TCGA-FS-A1ZS-10A-01D-A199-08 g.chr17:18139963G>A c.1395G>A c.(1393-1395)gtG>gtA p.V465V SKCM 17 18140840 18140840 + Missense_Mutation SNP A A T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr17:18140840A>T c.1657A>T c.(1657-1659)Agc>Tgc p.S553C SKCM 17 18140908 18140908 + Silent SNP C C T TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr17:18140908C>T c.1725C>T c.(1723-1725)agC>agT p.S575S SKCM 17 18140988 18140988 + Missense_Mutation SNP C C T TCGA-DA-A1I7-06A-22D-A197-08 TCGA-DA-A1I7-10A-01D-A199-08 g.chr17:18140988C>T c.1805C>T c.(1804-1806)aCc>aTc p.T602I SKCM 17 18143908 18143908 + Silent SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr17:18143908C>T c.2223C>T c.(2221-2223)ccC>ccT p.P741P SKCM 17 18143971 18143971 + Silent SNP A A G TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr17:18143971A>G c.2286A>G c.(2284-2286)gcA>gcG p.A762A

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 17 18137141 18137141 single base substitution A G missense_variant S148G 442A>G BLCA-CN 17 18137141 18137141 single base substitution A G upstream_gene_variant BLCA-CN 17 18148541 18148541 single base substitution G A downstream_gene_variant BLCA-US 17 18137636 18137636 single base substitution C T exon_variant BLCA-US 17 18137636 18137636 single base substitution C T missense_variant S255L 764C>T BRCA-EU 17 18124030 18124030 single base substitution G T upstream_gene_variant BRCA-EU 17 18125515 18125559 multiple base substitution (>=2bp and <=200bp) AATTAGCTGGGCATGGTGGCACAGACCTATAGTCCCAGCTACTCA ATCAGCTGAGTGTGGTGGCGCATGCCTATAGTCCAAGCTACTTG upstream_gene_variant BRCA-EU 17 18125608 18125608 single base substitution G C upstream_gene_variant BRCA-EU 17 18126687 18126687 single base substitution A T upstream_gene_variant BRCA-EU 17 18126889 18126889 single base substitution T G upstream_gene_variant BRCA-EU 17 18126916 18126916 single base substitution T G upstream_gene_variant BRCA-EU 17 18129251 18129251 single base substitution C A intron_variant BRCA-EU 17 18129944 18129944 single base substitution G A intron_variant BRCA-EU 17 18140576 18140576 insertion of <=200bp - G exon_variant BRCA-EU 17 18140576 18140576 insertion of <=200bp - G intron_variant BRCA-EU 17 18140844 18140844 single base substitution T C exon_variant BRCA-EU 17 18140844 18140844 single base substitution T C missense_variant V554A 1661T>C BRCA-EU 17 18147487 18147509 deletion of <=200bp CCCAGCACCTGTGCCACCTCCCC - 3_prime_UTR_variant BRCA-EU 17 18147487 18147509 deletion of <=200bp CCCAGCACCTGTGCCACCTCCCC - exon_variant BRCA-EU 17 18147656 18147656 single base substitution C T 3_prime_UTR_variant BRCA-EU 17 18147656 18147656 single base substitution C T exon_variant BRCA-EU 17 18151840 18151840 single base substitution G T downstream_gene_variant BRCA-EU 17 18152573 18152573 single base substitution C A downstream_gene_variant BRCA-FR 17 18150339 18150339 single base substitution C T downstream_gene_variant BRCA-UK 17 18149416 18149416 single base substitution C G downstream_gene_variant BRCA-US 17 18138574 18138574 single base substitution G A exon_variant BRCA-US 17 18138574 18138574 single base substitution G A missense_variant R411H 1232G>A BRCA-US 17 18140040 18140042 deletion of <=200bp AGG - disruptive_inframe_deletion QA491P BRCA-US 17 18140040 18140042 deletion of <=200bp AGG - exon_variant BRCA-US 17 18140048 18140050 deletion of <=200bp GAG - exon_variant BRCA-US 17 18140048 18140050 deletion of <=200bp GAG - inframe_deletion E494 BRCA-US 17 18145296 18145296 single base substitution C T exon_variant BRCA-US 17 18145296 18145296 single base substitution C T synonymous_variant R955R 2865C>T BRCA-US 17 18145941 18145941 single base substitution G C missense_variant G1039R 3115G>C BRCA-US 17 18145941 18145941 single base substitution G C splice_region_variant BRCA-US 17 18146095 18146095 single base substitution C A exon_variant BRCA-US 17 18146095 18146095 single base substitution C A missense_variant A1052E 3155C>A BRCA-US 17 18148916 18148916 single base substitution C G downstream_gene_variant BRCA-US 17 18149307 18149307 single base substitution C T downstream_gene_variant BRCA-US 17 18149365 18149365 single base substitution C T downstream_gene_variant BRCA-US 17 18149711 18149711 single base substitution G A downstream_gene_variant BRCA-US 17 18149770 18149770 single base substitution G A downstream_gene_variant BTCA-JP 17 18138321 18138321 single base substitution C T intron_variant BTCA-JP 17 18144921 18144921 single base substitution G A exon_variant BTCA-JP 17 18144921 18144921 single base substitution G A missense_variant V887I 2659G>A BTCA-JP 17 18148841 18148841 single base substitution A G downstream_gene_variant BTCA-JP 17 18148995 18148995 single base substitution T C downstream_gene_variant BTCA-JP 17 18150373 18150373 single base substitution G A downstream_gene_variant BTCA-JP 17 18150609 18150609 single base substitution C T downstream_gene_variant BTCA-JP 17 18151200 18151200 single base substitution C T downstream_gene_variant CESC-US 17 18138202 18138202 single base substitution G A exon_variant CESC-US 17 18138202 18138202 single base substitution G A missense_variant D319N 955G>A CESC-US 17 18141887 18141887 single base substitution C T exon_variant CESC-US 17 18141887 18141887 single base substitution C T missense_variant R724C 2170C>T CESC-US 17 18150641 18150641 single base substitution C T downstream_gene_variant CLLE-ES 17 18129442 18129442 single base substitution G A intron_variant CLLE-ES 17 18145294 18145294 single base substitution C T exon_variant CLLE-ES 17 18145294 18145294 single base substitution C T missense_variant R955C 2863C>T COAD-US 17 18135989 18135989 single base substitution C T missense_variant R89C 265C>T COAD-US 17 18135989 18135989 single base substitution C T upstream_gene_variant COAD-US 17 18138798 18138798 insertion of <=200bp - G exon_variant COAD-US 17 18138798 18138798 insertion of <=200bp - G frameshift_variant T433T? COAD-US 17 18141423 18141423 single base substitution G A exon_variant COAD-US 17 18141423 18141423 single base substitution G A synonymous_variant P649P 1947G>A COAD-US 17 18144014 18144014 single base substitution G A exon_variant COAD-US 17 18144014 18144014 single base substitution G A missense_variant V777M 2329G>A COAD-US 17 18144975 18144975 single base substitution C T exon_variant COAD-US 17 18144975 18144975 single base substitution C T missense_variant R905W 2713C>T COAD-US 17 18145296 18145296 single base substitution C T exon_variant COAD-US 17 18145296 18145296 single base substitution C T synonymous_variant R955R 2865C>T COAD-US 17 18148485 18148485 single base substitution G A downstream_gene_variant COAD-US 17 18149941 18149941 single base substitution C G downstream_gene_variant COAD-US 17 18150606 18150606 single base substitution C T downstream_gene_variant COCA-CN 17 18137405 18137405 single base substitution G T exon_variant COCA-CN 17 18137405 18137405 single base substitution G T missense_variant K210N 630G>T COCA-CN 17 18138285 18138285 single base substitution G A exon_variant COCA-CN 17 18138285 18138285 single base substitution G A synonymous_variant V346V 1038G>A COCA-CN 17 18139896 18139896 single base substitution G T exon_variant COCA-CN 17 18139896 18139896 single base substitution G T intron_variant COCA-CN 17 18140077 18140077 single base substitution G A splice_region_variant COCA-CN 17 18141887 18141887 single base substitution C T exon_variant COCA-CN 17 18141887 18141887 single base substitution C T missense_variant R724C 2170C>T COCA-CN 17 18144167 18144167 single base substitution G A exon_variant COCA-CN 17 18144167 18144167 single base substitution G A missense_variant A828T 2482G>A COCA-CN 17 18145986 18145986 single base substitution C A intron_variant COCA-CN 17 18148568 18148568 single base substitution G A downstream_gene_variant COCA-CN 17 18148831 18148831 single base substitution G A downstream_gene_variant COCA-CN 17 18151069 18151069 single base substitution G A downstream_gene_variant COCA-CN 17 18151078 18151078 single base substitution G A downstream_gene_variant COCA-CN 17 18151108 18151108 single base substitution C T downstream_gene_variant EOPC-DE 17 18143545 18143545 single base substitution G A intron_variant EOPC-DE 17 18151954 18151954 single base substitution T A downstream_gene_variant ESAD-UK 17 18124464 18124464 insertion of <=200bp - C upstream_gene_variant ESAD-UK 17 18128063 18128065 deletion of <=200bp CCA - upstream_gene_variant ESAD-UK 17 18128068 18128070 deletion of <=200bp GTC - upstream_gene_variant ESAD-UK 17 18130476 18130476 single base substitution G C intron_variant ESAD-UK 17 18131552 18131552 single base substitution T C intron_variant ESAD-UK 17 18132654 18132654 single base substitution G A intron_variant ESAD-UK 17 18132654 18132654 single base substitution G A upstream_gene_variant ESAD-UK 17 18134965 18134965 insertion of <=200bp - T intron_variant ESAD-UK 17 18134965 18134965 insertion of <=200bp - T upstream_gene_variant ESAD-UK 17 18137931 18137931 single base substitution T C intron_variant ESAD-UK 17 18138321 18138321 single base substitution C T intron_variant ESAD-UK 17 18142824 18142824 insertion of <=200bp - T intron_variant ESAD-UK 17 18147118 18147120 deletion of <=200bp GAG - intron_variant ESAD-UK 17 18151685 18151690 deletion of <=200bp CTACTT - downstream_gene_variant ESAD-UK 17 18151861 18151861 single base substitution C T downstream_gene_variant ESAD-UK 17 18152271 18152271 deletion of <=200bp A - downstream_gene_variant ESCA-CN 17 18137845 18137845 single base substitution G A intron_variant ESCA-CN 17 18140069 18140069 single base substitution C T exon_variant ESCA-CN 17 18140069 18140069 single base substitution C T missense_variant R501C 1501C>T ESCA-CN 17 18144934 18144934 single base substitution C T exon_variant ESCA-CN 17 18144934 18144934 single base substitution C T missense_variant S891L 2672C>T GBM-US 17 18135847 18135847 single base substitution G A missense_variant R73Q 218G>A GBM-US 17 18135847 18135847 single base substitution G A upstream_gene_variant GBM-US 17 18138556 18138556 single base substitution C G exon_variant GBM-US 17 18138556 18138556 single base substitution C G missense_variant P405R 1214C>G KIRC-US 17 18135884 18135884 single base substitution C T synonymous_variant T85T 255C>T KIRC-US 17 18135884 18135884 single base substitution C T upstream_gene_variant KIRC-US 17 18136083 18136083 single base substitution A G missense_variant Q120R 359A>G KIRC-US 17 18136083 18136083 single base substitution A G upstream_gene_variant KIRC-US 17 18137246 18137246 single base substitution C T exon_variant KIRC-US 17 18137246 18137246 single base substitution C T missense_variant R183C 547C>T KIRC-US 17 18141525 18141525 insertion of <=200bp - A exon_variant KIRC-US 17 18141525 18141525 insertion of <=200bp - A frameshift_variant S683R? KIRP-US 17 18149935 18149935 single base substitution G A downstream_gene_variant KIRP-US 17 18150014 18150014 single base substitution C T downstream_gene_variant KIRP-US 17 18150655 18150655 single base substitution A C downstream_gene_variant LAML-KR 17 18125603 18125603 single base substitution T C upstream_gene_variant LAML-KR 17 18143714 18143714 single base substitution A G intron_variant LAML-KR 17 18143922 18143922 single base substitution G A exon_variant LAML-KR 17 18143922 18143922 single base substitution G A missense_variant G746D 2237G>A LAML-KR 17 18145450 18145450 single base substitution A G intron_variant LAML-KR 17 18148485 18148485 single base substitution G A downstream_gene_variant LICA-FR 17 18127186 18127186 single base substitution T C upstream_gene_variant LICA-FR 17 18127194 18127194 single base substitution T C upstream_gene_variant LICA-FR 17 18138792 18138792 single base substitution C T exon_variant LICA-FR 17 18138792 18138792 single base substitution C T synonymous_variant P431P 1293C>T LICA-FR 17 18144003 18144003 single base substitution C T exon_variant LICA-FR 17 18144003 18144003 single base substitution C T missense_variant A773V 2318C>T LICA-FR 17 18148958 18148958 single base substitution C T downstream_gene_variant LINC-JP 17 18133123 18133123 single base substitution C T intron_variant LINC-JP 17 18133123 18133123 single base substitution C T upstream_gene_variant LINC-JP 17 18137234 18137234 single base substitution G A exon_variant LINC-JP 17 18137234 18137234 single base substitution G A missense_variant G179S 535G>A LINC-JP 17 18144056 18144056 single base substitution G T exon_variant LINC-JP 17 18144056 18144056 single base substitution G T missense_variant V791L 2371G>T LINC-JP 17 18151337 18151337 single base substitution C A downstream_gene_variant LINC-JP 17 18152414 18152414 deletion of <=200bp C - downstream_gene_variant LIRI-JP 17 18125147 18125147 single base substitution C G upstream_gene_variant LIRI-JP 17 18125267 18125267 single base substitution C A upstream_gene_variant LIRI-JP 17 18126138 18126138 single base substitution G A upstream_gene_variant LIRI-JP 17 18127160 18127160 single base substitution T A upstream_gene_variant LIRI-JP 17 18127166 18127166 single base substitution C T upstream_gene_variant LIRI-JP 17 18128041 18128041 single base substitution A G upstream_gene_variant LIRI-JP 17 18128433 18128433 single base substitution C A upstream_gene_variant LIRI-JP 17 18134682 18134682 single base substitution G T intron_variant LIRI-JP 17 18134682 18134682 single base substitution G T upstream_gene_variant LIRI-JP 17 18134822 18134822 single base substitution G A intron_variant LIRI-JP 17 18134822 18134822 single base substitution G A upstream_gene_variant LIRI-JP 17 18135772 18135772 single base substitution G C intron_variant LIRI-JP 17 18135772 18135772 single base substitution G C upstream_gene_variant LIRI-JP 17 18138162 18138162 single base substitution T C exon_variant LIRI-JP 17 18138162 18138162 single base substitution T C synonymous_variant F305F 915T>C LIRI-JP 17 18139475 18139475 single base substitution G A exon_variant LIRI-JP 17 18139475 18139475 single base substitution G A intron_variant LIRI-JP 17 18146746 18146746 single base substitution A T intron_variant LIRI-JP 17 18151948 18151955 deletion of <=200bp GAACTCTG - downstream_gene_variant LUSC-KR 17 18138698 18138698 single base substitution G T intron_variant LUSC-KR 17 18144270 18144270 single base substitution A C exon_variant LUSC-KR 17 18144270 18144270 single base substitution A C intron_variant LUSC-KR 17 18145450 18145450 single base substitution A G intron_variant LUSC-KR 17 18148485 18148485 single base substitution G A downstream_gene_variant LUSC-KR 17 18151424 18151424 single base substitution C G downstream_gene_variant LUSC-US 17 18136004 18136004 single base substitution C A missense_variant L94I 280C>A LUSC-US 17 18136004 18136004 single base substitution C A upstream_gene_variant LUSC-US 17 18148479 18148479 single base substitution C G downstream_gene_variant LUSC-US 17 18148710 18148710 single base substitution C G downstream_gene_variant LUSC-US 17 18148904 18148904 single base substitution C T downstream_gene_variant LUSC-US 17 18149623 18149623 single base substitution G A downstream_gene_variant LUSC-US 17 18149711 18149711 single base substitution G A downstream_gene_variant MALY-DE 17 18126883 18126883 insertion of <=200bp - T upstream_gene_variant MALY-DE 17 18130510 18130510 single base substitution G A intron_variant MALY-DE 17 18133132 18133132 single base substitution C T intron_variant MALY-DE 17 18133132 18133132 single base substitution C T upstream_gene_variant MALY-DE 17 18133933 18133933 single base substitution C T intron_variant MALY-DE 17 18133933 18133933 single base substitution C T upstream_gene_variant MALY-DE 17 18137614 18137614 single base substitution G A exon_variant MALY-DE 17 18137614 18137614 single base substitution G A missense_variant D248N 742G>A MELA-AU 17 18123973 18123973 single base substitution C T upstream_gene_variant MELA-AU 17 18124013 18124013 single base substitution G C upstream_gene_variant MELA-AU 17 18124135 18124135 single base substitution G A upstream_gene_variant MELA-AU 17 18124191 18124191 single base substitution C T upstream_gene_variant MELA-AU 17 18124353 18124353 single base substitution G A upstream_gene_variant MELA-AU 17 18124446 18124446 single base substitution G A upstream_gene_variant MELA-AU 17 18124826 18124826 single base substitution A G upstream_gene_variant MELA-AU 17 18125301 18125301 single base substitution C T upstream_gene_variant MELA-AU 17 18125462 18125462 single base substitution C T upstream_gene_variant MELA-AU 17 18125549 18125549 single base substitution C T upstream_gene_variant MELA-AU 17 18125773 18125773 single base substitution A C upstream_gene_variant MELA-AU 17 18126148 18126148 single base substitution T C upstream_gene_variant MELA-AU 17 18126346 18126346 single base substitution C T upstream_gene_variant MELA-AU 17 18126754 18126754 single base substitution A C upstream_gene_variant MELA-AU 17 18126758 18126758 single base substitution C A upstream_gene_variant MELA-AU 17 18126762 18126762 single base substitution G A upstream_gene_variant MELA-AU 17 18126805 18126805 single base substitution C T upstream_gene_variant MELA-AU 17 18129770 18129770 single base substitution C T intron_variant MELA-AU 17 18130256 18130256 single base substitution G A intron_variant MELA-AU 17 18130794 18130794 single base substitution C T intron_variant MELA-AU 17 18132121 18132121 single base substitution C T intron_variant MELA-AU 17 18132549 18132549 single base substitution T G intron_variant MELA-AU 17 18132549 18132549 single base substitution T G upstream_gene_variant MELA-AU 17 18133785 18133785 single base substitution G A intron_variant MELA-AU 17 18133785 18133785 single base substitution G A upstream_gene_variant MELA-AU 17 18133885 18133885 single base substitution C T intron_variant MELA-AU 17 18133885 18133885 single base substitution C T upstream_gene_variant MELA-AU 17 18134134 18134134 single base substitution C T intron_variant MELA-AU 17 18134134 18134134 single base substitution C T upstream_gene_variant MELA-AU 17 18134460 18134461 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 17 18134460 18134461 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 17 18135491 18135491 single base substitution G A intron_variant MELA-AU 17 18135491 18135491 single base substitution G A upstream_gene_variant MELA-AU 17 18136830 18136830 single base substitution C T intron_variant MELA-AU 17 18136830 18136830 single base substitution C T upstream_gene_variant MELA-AU 17 18137185 18137185 single base substitution C T synonymous_variant F162F 486C>T MELA-AU 17 18137185 18137185 single base substitution C T upstream_gene_variant MELA-AU 17 18137477 18137477 single base substitution C T exon_variant MELA-AU 17 18137477 18137477 single base substitution C T synonymous_variant F234F 702C>T MELA-AU 17 18138060 18138060 single base substitution T C intron_variant MELA-AU 17 18140161 18140161 single base substitution G A exon_variant MELA-AU 17 18140161 18140161 single base substitution G A missense_variant D507N 1519G>A MELA-AU 17 18140684 18140684 single base substitution C T exon_variant MELA-AU 17 18140684 18140684 single base substitution C T intron_variant MELA-AU 17 18140908 18140908 single base substitution C T exon_variant MELA-AU 17 18140908 18140908 single base substitution C T synonymous_variant S575S 1725C>T MELA-AU 17 18141404 18141404 single base substitution C T exon_variant MELA-AU 17 18141404 18141404 single base substitution C T missense_variant S643F 1928C>T MELA-AU 17 18141440 18141440 single base substitution C T exon_variant MELA-AU 17 18141440 18141440 single base substitution C T missense_variant S655F 1964C>T MELA-AU 17 18141567 18141567 single base substitution C T intron_variant MELA-AU 17 18141917 18141917 single base substitution C T exon_variant MELA-AU 17 18141917 18141917 single base substitution C T stop_gained R734* 2200C>T MELA-AU 17 18142282 18142282 single base substitution A G intron_variant MELA-AU 17 18142457 18142457 deletion of <=200bp T - intron_variant MELA-AU 17 18142607 18142607 single base substitution G A intron_variant MELA-AU 17 18143640 18143640 single base substitution C T intron_variant MELA-AU 17 18144312 18144312 single base substitution C T exon_variant MELA-AU 17 18144312 18144312 single base substitution C T intron_variant MELA-AU 17 18145367 18145367 single base substitution C T intron_variant MELA-AU 17 18145447 18145448 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 17 18145571 18145572 multiple base substitution (>=2bp and <=200bp) CC AT exon_variant MELA-AU 17 18145571 18145572 multiple base substitution (>=2bp and <=200bp) CC AT missense_variant P992I 2974CC>AT MELA-AU 17 18145967 18145967 deletion of <=200bp G - intron_variant MELA-AU 17 18147790 18147790 single base substitution C T 3_prime_UTR_variant MELA-AU 17 18147790 18147790 single base substitution C T exon_variant MELA-AU 17 18149169 18149169 single base substitution G A downstream_gene_variant MELA-AU 17 18149171 18149171 single base substitution G A downstream_gene_variant MELA-AU 17 18149498 18149498 single base substitution G A downstream_gene_variant MELA-AU 17 18151043 18151043 single base substitution C T downstream_gene_variant MELA-AU 17 18151482 18151482 single base substitution G A downstream_gene_variant MELA-AU 17 18151742 18151742 single base substitution G A downstream_gene_variant MELA-AU 17 18153031 18153031 single base substitution G A downstream_gene_variant MELA-AU 17 18153121 18153121 single base substitution C G downstream_gene_variant MELA-AU 17 18153135 18153135 single base substitution C A downstream_gene_variant ORCA-IN 17 18142970 18142970 single base substitution C T intron_variant ORCA-IN 17 18144030 18144030 single base substitution T G exon_variant ORCA-IN 17 18144030 18144030 single base substitution T G missense_variant V782G 2345T>G OV-AU 17 18125078 18125078 single base substitution G T upstream_gene_variant OV-AU 17 18133053 18133053 single base substitution G T intron_variant OV-AU 17 18133053 18133053 single base substitution G T upstream_gene_variant OV-AU 17 18147289 18147289 single base substitution G A 3_prime_UTR_variant OV-AU 17 18147289 18147289 single base substitution G A exon_variant OV-AU 17 18150290 18150290 single base substitution G C downstream_gene_variant PACA-AU 17 18126302 18126302 single base substitution C T upstream_gene_variant PACA-AU 17 18126897 18126897 single base substitution G T upstream_gene_variant PACA-AU 17 18133353 18133353 single base substitution G A splice_donor_variant PACA-AU 17 18133353 18133353 single base substitution G A upstream_gene_variant PACA-AU 17 18147608 18147608 single base substitution T G 3_prime_UTR_variant PACA-AU 17 18147608 18147608 single base substitution T G exon_variant PACA-AU 17 18151066 18151066 single base substitution C T downstream_gene_variant PACA-AU 17 18151094 18151094 single base substitution G A downstream_gene_variant PACA-CA 17 18126444 18126444 single base substitution C T upstream_gene_variant PACA-CA 17 18127380 18127380 single base substitution G C upstream_gene_variant PACA-CA 17 18128107 18128107 single base substitution G A upstream_gene_variant PACA-CA 17 18137494 18137494 single base substitution G A splice_region_variant PACA-CA 17 18144639 18144639 single base substitution C T exon_variant PACA-CA 17 18144639 18144639 single base substitution C T intron_variant PACA-CA 17 18146194 18146194 single base substitution C T intron_variant PACA-CA 17 18150537 18150537 single base substitution C G downstream_gene_variant PACA-CA 17 18150775 18150775 single base substitution G A downstream_gene_variant PAEN-AU 17 18127339 18127339 single base substitution T A upstream_gene_variant PAEN-AU 17 18134451 18134451 single base substitution G A intron_variant PAEN-AU 17 18134451 18134451 single base substitution G A upstream_gene_variant PAEN-AU 17 18151466 18151466 single base substitution C T downstream_gene_variant PAEN-IT 17 18138606 18138606 single base substitution C A exon_variant PAEN-IT 17 18138606 18138606 single base substitution C A missense_variant Q422K 1264C>A PBCA-DE 17 18129708 18129708 single base substitution A C intron_variant PBCA-DE 17 18147304 18147305 deletion of <=200bp AT - 3_prime_UTR_variant PBCA-DE 17 18147304 18147305 deletion of <=200bp AT - exon_variant PRAD-CA 17 18125767 18125767 single base substitution C T upstream_gene_variant PRAD-CA 17 18153138 18153138 single base substitution A C downstream_gene_variant PRAD-UK 17 18129974 18129974 single base substitution C T intron_variant PRAD-UK 17 18147481 18147496 deletion of <=200bp GTGGGGCCCAGCACCT - 3_prime_UTR_variant PRAD-UK 17 18147481 18147496 deletion of <=200bp GTGGGGCCCAGCACCT - exon_variant PRAD-US 17 18137336 18137336 single base substitution C T exon_variant PRAD-US 17 18137336 18137336 single base substitution C T synonymous_variant D187D 561C>T PRAD-US 17 18150040 18150042 deletion of <=200bp CTC - downstream_gene_variant PRAD-US 17 18151872 18151872 single base substitution G C downstream_gene_variant READ-US 17 18149086 18149086 single base substitution C T downstream_gene_variant READ-US 17 18151144 18151144 single base substitution T C downstream_gene_variant SKCA-BR 17 18124519 18124519 single base substitution T C upstream_gene_variant SKCA-BR 17 18125245 18125245 single base substitution T C upstream_gene_variant SKCA-BR 17 18125685 18125685 single base substitution A T upstream_gene_variant SKCA-BR 17 18127415 18127415 single base substitution C T upstream_gene_variant SKCA-BR 17 18128397 18128397 single base substitution T G upstream_gene_variant SKCA-BR 17 18129112 18129112 single base substitution A G intron_variant SKCA-BR 17 18129167 18129167 single base substitution C G intron_variant SKCA-BR 17 18129266 18129266 single base substitution T G intron_variant SKCA-BR 17 18130709 18130709 insertion of <=200bp - CT intron_variant SKCA-BR 17 18131207 18131207 single base substitution C T intron_variant SKCA-BR 17 18133139 18133139 single base substitution C T intron_variant SKCA-BR 17 18133139 18133139 single base substitution C T upstream_gene_variant SKCA-BR 17 18133337 18133337 single base substitution C T missense_variant S55F 164C>T SKCA-BR 17 18133337 18133337 single base substitution C T upstream_gene_variant SKCA-BR 17 18133906 18133906 single base substitution T G intron_variant SKCA-BR 17 18133906 18133906 single base substitution T G upstream_gene_variant SKCA-BR 17 18135753 18135753 single base substitution T C intron_variant SKCA-BR 17 18135753 18135753 single base substitution T C upstream_gene_variant SKCA-BR 17 18138499 18138499 single base substitution A C exon_variant SKCA-BR 17 18138499 18138499 single base substitution A C missense_variant Y386S 1157A>C SKCA-BR 17 18138671 18138671 single base substitution G A intron_variant SKCA-BR 17 18140111 18140111 single base substitution A C intron_variant SKCA-BR 17 18147555 18147555 insertion of <=200bp - CT 3_prime_UTR_variant SKCA-BR 17 18147555 18147555 insertion of <=200bp - CT exon_variant SKCM-US 17 18137373 18137373 single base substitution T G exon_variant SKCM-US 17 18137373 18137373 single base substitution T G missense_variant S200A 598T>G SKCM-US 17 18137691 18137691 single base substitution G A exon_variant SKCM-US 17 18137691 18137691 single base substitution G A synonymous_variant T273T 819G>A SKCM-US 17 18138301 18138301 single base substitution G A exon_variant SKCM-US 17 18138301 18138301 single base substitution G A missense_variant E352K 1054G>A SKCM-US 17 18138547 18138547 single base substitution C T exon_variant SKCM-US 17 18138547 18138547 single base substitution C T missense_variant A402V 1205C>T SKCM-US 17 18139963 18139963 single base substitution G A exon_variant SKCM-US 17 18139963 18139963 single base substitution G A synonymous_variant V465V 1395G>A SKCM-US 17 18140840 18140840 single base substitution A T exon_variant SKCM-US 17 18140840 18140840 single base substitution A T missense_variant S553C 1657A>T SKCM-US 17 18140908 18140908 single base substitution C T exon_variant SKCM-US 17 18140908 18140908 single base substitution C T synonymous_variant S575S 1725C>T SKCM-US 17 18140988 18140988 single base substitution C T exon_variant SKCM-US 17 18140988 18140988 single base substitution C T missense_variant T602I 1805C>T SKCM-US 17 18143908 18143908 single base substitution C T exon_variant SKCM-US 17 18143908 18143908 single base substitution C T synonymous_variant P741P 2223C>T SKCM-US 17 18143971 18143971 single base substitution A G exon_variant SKCM-US 17 18143971 18143971 single base substitution A G synonymous_variant A762A 2286A>G SKCM-US 17 18148563 18148563 single base substitution G A downstream_gene_variant SKCM-US 17 18149956 18149956 single base substitution G A downstream_gene_variant SKCM-US 17 18150582 18150582 single base substitution G A downstream_gene_variant SKCM-US 17 18150990 18150990 single base substitution A G downstream_gene_variant SKCM-US 17 18151073 18151073 single base substitution C T downstream_gene_variant STAD-US 17 18133328 18133328 single base substitution G A missense_variant G52D 155G>A STAD-US 17 18133328 18133328 single base substitution G A upstream_gene_variant STAD-US 17 18136088 18136088 single base substitution C T missense_variant P122S 364C>T STAD-US 17 18136088 18136088 single base substitution C T upstream_gene_variant STAD-US 17 18138263 18138263 single base substitution G A exon_variant STAD-US 17 18138263 18138263 single base substitution G A missense_variant R339H 1016G>A STAD-US 17 18140176 18140176 single base substitution G A exon_variant STAD-US 17 18140176 18140176 single base substitution G A missense_variant D512N 1534G>A STAD-US 17 18140801 18140801 single base substitution G A exon_variant STAD-US 17 18140801 18140801 single base substitution G A missense_variant V540I 1618G>A STAD-US 17 18140896 18140896 single base substitution C T exon_variant STAD-US 17 18140896 18140896 single base substitution C T synonymous_variant H571H 1713C>T STAD-US 17 18140961 18140961 single base substitution T C exon_variant STAD-US 17 18140961 18140961 single base substitution T C missense_variant V593A 1778T>C STAD-US 17 18140983 18140983 single base substitution T A exon_variant STAD-US 17 18140983 18140983 single base substitution T A synonymous_variant A600A 1800T>A STAD-US 17 18141431 18141431 single base substitution G A exon_variant STAD-US 17 18141431 18141431 single base substitution G A missense_variant R652Q 1955G>A STAD-US 17 18143909 18143909 single base substitution A G exon_variant STAD-US 17 18143909 18143909 single base substitution A G missense_variant T742A 2224A>G STAD-US 17 18144927 18144927 single base substitution G A exon_variant STAD-US 17 18144927 18144927 single base substitution G A missense_variant V889I 2665G>A STAD-US 17 18145266 18145266 single base substitution G T exon_variant STAD-US 17 18145266 18145266 single base substitution G T synonymous_variant P945P 2835G>T STAD-US 17 18148464 18148464 single base substitution C A downstream_gene_variant STAD-US 17 18148506 18148506 single base substitution G A downstream_gene_variant STAD-US 17 18148975 18148975 single base substitution C A downstream_gene_variant STAD-US 17 18150517 18150517 deletion of <=200bp A - downstream_gene_variant STAD-US 17 18151054 18151054 single base substitution T C downstream_gene_variant STAD-US 17 18151293 18151293 single base substitution C T downstream_gene_variant STAD-US 17 18152148 18152148 insertion of <=200bp - C downstream_gene_variant STAD-US 17 18152659 18152659 single base substitution C G downstream_gene_variant THCA-SA 17 18148944 18148944 single base substitution C G downstream_gene_variant THCA-US 17 18149316 18149316 single base substitution C T downstream_gene_variant THCA-US 17 18150552 18150552 single base substitution C G downstream_gene_variant UCEC-US 17 18137422 18137422 single base substitution G A exon_variant UCEC-US 17 18137422 18137422 single base substitution G A missense_variant S216N 647G>A UCEC-US 17 18137994 18137994 single base substitution T G exon_variant UCEC-US 17 18137994 18137994 single base substitution T G missense_variant I294M 882T>G UCEC-US 17 18140155 18140155 single base substitution T A exon_variant UCEC-US 17 18140155 18140155 single base substitution T A missense_variant C505S 1513T>A UCEC-US 17 18141458 18141458 single base substitution G A exon_variant UCEC-US 17 18141458 18141458 single base substitution G A missense_variant R661H 1982G>A UCEC-US 17 18141888 18141888 single base substitution G A exon_variant UCEC-US 17 18141888 18141888 single base substitution G A missense_variant R724H 2171G>A UCEC-US 17 18144167 18144167 single base substitution G A exon_variant UCEC-US 17 18144167 18144167 single base substitution G A missense_variant A828T 2482G>A UCEC-US 17 18144999 18144999 single base substitution G A exon_variant UCEC-US 17 18144999 18144999 single base substitution G A missense_variant A913T 2737G>A UCEC-US 17 18145004 18145004 single base substitution G A exon_variant UCEC-US 17 18145004 18145004 single base substitution G A synonymous_variant S914S 2742G>A UCEC-US 17 18145007 18145007 single base substitution C T exon_variant UCEC-US 17 18145007 18145007 single base substitution C T synonymous_variant C915C 2745C>T UCEC-US 17 18145018 18145018 single base substitution G A exon_variant UCEC-US 17 18145018 18145018 single base substitution G A missense_variant R919H 2756G>A UCEC-US 17 18145300 18145300 single base substitution G A exon_variant UCEC-US 17 18145300 18145300 single base substitution G A missense_variant A957T 2869G>A UCEC-US 17 18146112 18146112 single base substitution G A exon_variant UCEC-US 17 18146112 18146112 single base substitution G A missense_variant A1058T 3172G>A UCEC-US 17 18148549 18148549 single base substitution C T downstream_gene_variant UCEC-US 17 18148671 18148671 single base substitution G A downstream_gene_variant UCEC-US 17 18150106 18150106 single base substitution C A downstream_gene_variant UCEC-US 17 18150119 18150119 single base substitution T G downstream_gene_variant UCEC-US 17 18150566 18150566 single base substitution G A downstream_gene_variant UCEC-US 17 18151094 18151094 single base substitution G A downstream_gene_variant UCEC-US 17 18151108 18151108 single base substitution C T downstream_gene_variant UCEC-US 17 18151272 18151272 single base substitution T C downstream_gene_variant UCEC-US 17 18151970 18151970 single base substitution T C downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 2292383 COSM4610238 c.2746G>A p.V916I Substitution - Missense 17:18241694-18241694 + CPCG0083-F1 COSM4880206 c.1190G>A p.R397Q Substitution - Missense 17:7196779-7196779 - TCGA-BG-A18B-01 COSM976256 c.2869G>A p.A957T Substitution - Missense 17:18241986-18241986 + PTC-14C COSM4129648 c.104A>G p.N35S Substitution - Missense 17:18229963-18229963 + TCGA-BR-4292-01 COSM4069173 c.635-1G>A p.? Unknown 17:7203330-7203330 - BD57T COSM5055283 c.2659G>A p.V887I Substitution - Missense 17:18241607-18241607 + CSCC-27-T COSM4512313 c.899C>T p.P300L Substitution - Missense 17:7202920-7202920 - TCGA-06-5858-01 COSM117029 c.1676G>A p.R559Q Substitution - Missense 17:7193711-7193711 - TCGA-39-5031-01 COSM707417 c.2013C>T p.L671L Substitution - coding silent 17:7191985-7191985 - TCGA-AU-6004-01 COSM436149 c.2865C>T p.R955R Substitution - coding silent 17:18241982-18241982 + 587228 COSM1203715 c.1840C>T p.R614W Substitution - Missense 17:7193100-7193100 - TCGA-21-5787-01 COSM707415 c.1126G>C p.G376R Substitution - Missense 17:7196843-7196843 - 012-02-1TD COSM96804 c.2863C>T p.R955C Substitution - Missense 17:18241980-18241980 + CSCC-10-T COSM4526283 c.1386G>A p.G462G Substitution - coding silent 17:7196264-7196264 - TCGA-A3-3363-01 COSM1493864 c.2708G>A p.C903Y Substitution - Missense 17:18241656-18241656 + B77-Tumor COSM1563388 c.442A>G p.S148G Substitution - Missense 17:18233827-18233827 + Au1 COSM5596981 c.1537C>T p.P513S Substitution - Missense 17:18236865-18236865 + ESCC-180T COSM3937277 c.1501C>T p.R501C Substitution - Missense 17:18236755-18236755 + I2L-P19Tb-Tumor-Organoid COSM5364116 c.2101G>A p.V701M Substitution - Missense 17:18238504-18238504 + HCC64T COSM1610700 c.53C>T p.P18L Substitution - Missense 17:7218606-7218606 - TCGA-AM-5821-01 COSM5134898 c.1673-6C>A p.? Unknown 17:7193720-7193720 - TCGA-CH-5738-01 COSM1128807 c.561C>T p.D187D Substitution - coding silent 17:18234022-18234022 + BD72T COSM5477007 c.1345G>A p.D449N Substitution - Missense 17:7196305-7196305 - TCGA-ER-A193-06 COSM3514900 c.1054G>A p.E352K Substitution - Missense 17:18234987-18234987 + CN-AML-NR-12-Dx COSM5424219 c.2237G>A p.G746D Substitution - Missense 17:18240608-18240608 + PT21_2 COSM3521561 c.998C>T p.S333F Substitution - Missense 17:7196971-7196971 - BCM399T COSM2740858 c.2318C>T p.A773V Substitution - Missense 17:18240689-18240689 + S02299 COSM5690339 c.1864G>C p.D622H Substitution - Missense 17:7193076-7193076 - TCGA-AZ-6598-01 COSM1385839 c.2080C>T p.R694C Substitution - Missense 17:7191918-7191918 - TCGA-DS-A0VM-01 COSM460248 c.1316-1G>C p.? Unknown 17:7196335-7196335 - TCGA-A6-6781-01 COSM1381311 c.265C>T p.R89C Substitution - Missense 17:18232675-18232675 + 36T COSM3718520 c.2345T>G p.V782G Substitution - Missense 17:18240716-18240716 + Pat_32_B COSM5853365 c.443C>T p.A148V Substitution - Missense 17:7203713-7203713 - TCGA-21-5784-01 COSM704824 c.280C>A p.L94I Substitution - Missense 17:18232690-18232690 + 419 COSM4431926 c.1603C>T p.R535W Substitution - Missense 17:7194323-7194323 - TCGA-CG-4306-01 COSM4064489 c.1618G>A p.V540I Substitution - Missense 17:18237487-18237487 + TCGA-DG-A2KL-01 COSM4851523 c.2170C>T p.R724C Substitution - Missense 17:18238573-18238573 + ESCC_BICR_005T COSM5439115 c.2672C>T p.S891L Substitution - Missense 17:18241620-18241620 + TCGA-A5-A0VP-01 COSM983782 c.961C>A p.L321M Substitution - Missense 17:7197008-7197008 - TCGA-29-2427-01 COSM80110 c.1230C>A p.A410A Substitution - coding silent 17:18235258-18235258 + CSCC-35-T COSM4569660 c.1921T>C p.F641L Substitution - Missense 17:7193019-7193019 - OSCC-GB_00610111 COSM4886859 c.609G>T p.E203D Substitution - Missense 17:7203449-7203449 - CN-AML-CR-36-Dx COSM5427519 c.1576G>A p.D526N Substitution - Missense 17:7194350-7194350 - TCGA-CG-4306-01 COSM4069170 c.2081G>A p.R694H Substitution - Missense 17:7191917-7191917 - 2492700 COSM5715501 c.2499C>A p.F833L Substitution - Missense 17:18240870-18240870 + PTC-28C COSM4130546 c.172C>A p.Q58K Substitution - Missense 17:7208227-7208227 - 587220 COSM1213448 c.607G>A p.G203R Substitution - Missense 17:18234068-18234068 + I2L-P19Tb-Tumor-Biopsy COSM5364116 c.2101G>A p.V701M Substitution - Missense 17:18238504-18238504 + COLO678 COSM2740832 c.650G>A p.R217Q Substitution - Missense 17:18234111-18234111 + 8066467 COSM3773022 c.535G>T p.A179S Substitution - Missense 17:7203523-7203523 - TCGA-EP-A2KB-01 COSM4921362 c.1448A>G p.D483G Substitution - Missense 17:7194478-7194478 - SC_9034 COSM5558736 c.510G>T p.L170L Substitution - coding silent 17:18233895-18233895 + YUKAT COSM5387183 c.2091C>T p.S697S Substitution - coding silent 17:7191907-7191907 - TCGA-20-1682-01 COSM1324126 c.1968C>T p.L656L Substitution - coding silent 17:18238130-18238130 + CME_0001_Pa_C COSM3378096 c.714+5G>A p.? Unknown 17:18234180-18234180 + TCGA-A6-6780-01 COSM1385824 c.2201T>C p.I734T Substitution - Missense 17:7190811-7190811 - DLD1 COSM4623493 c.2298T>C p.G766G Substitution - coding silent 17:18240669-18240669 + CSCC-49-T COSM4535289 c.2176G>A p.E726K Substitution - Missense 17:7191288-7191288 - QC2-32-T2 COSM3766166 c.1296C>T p.I432I Substitution - coding silent 17:7196492-7196492 - TCGA-A7-A5ZV-01 COSM3818970 c.1232G>A p.R411H Substitution - Missense 17:18235260-18235260 + SC_9099 COSM5567003 c.2686C>T p.R896W Substitution - Missense 17:18241634-18241634 + CSCC-27-T COSM4465777 c.139C>T p.R47C Substitution - Missense 17:18229998-18229998 + TCGA-A6-6780-01 COSM1385863 c.1245T>C p.H415H Substitution - coding silent 17:7196543-7196543 - TCGA-FG-6688-01 COSM3970269 c.622A>C p.K208Q Substitution - Missense 17:7203436-7203436 - CRC-19T COSM5481350 c.1038G>A p.V346V Substitution - coding silent 17:18234971-18234971 + 587376 COSM983778 c.1067G>A p.R356Q Substitution - Missense 17:7196902-7196902 - CSCC-6-T COSM4470689 c.1677C>T p.L559L Substitution - coding silent 17:18237546-18237546 + TCGA-NH-A5IV-01 COSM5182837 c.1476C>T p.S492S Substitution - coding silent 17:7194450-7194450 - TCGA-B0-5081-01 COSM472383 c.547C>T p.R183C Substitution - Missense 17:18233932-18233932 + TCGA-AR-A1AU-01 COSM436149 c.2865C>T p.R955R Substitution - coding silent 17:18241982-18241982 + I2L-P19Tb-Tumor-Organoid COSM5364111 c.2261T>C p.L754P Substitution - Missense 17:7190751-7190751 - TCGA-F4-6807-01 COSM1385894 c.439G>T p.A147S Substitution - Missense 17:7203717-7203717 - TCGA-02-2470-01 COSM3403176 c.27G>C p.R9S Substitution - Missense 17:7218632-7218632 - TCGA-CF-A3MG-01 COSM1302475 c.764C>T p.S255L Substitution - Missense 17:18234322-18234322 + TCGA-A8-A07E-01 COSM5833243 c.1472_1474delAGG p.Q491_A492>P Complex - deletion inframe 17:18236726-18236728 + CN-AML-12-T COSM5424219 c.2237G>A p.G746D Substitution - Missense 17:18240608-18240608 + HCC2998 COSM2976384 c.1290G>A p.T430T Substitution - coding silent 17:7196498-7196498 - TCGA-AM-5820-01 COSM3691404 c.1947G>A p.P649P Substitution - coding silent 17:18238109-18238109 + TCGA-F5-6814-01 COSM983778 c.1067G>A p.R356Q Substitution - Missense 17:7196902-7196902 - Gp2D COSM2740824 c.97T>C p.F33L Substitution - Missense 17:18229956-18229956 + TCGA-G4-6628-01 COSM5180150 c.150C>T p.A50A Substitution - coding silent 17:18230009-18230009 + TCGA-AA-3821-01 COSM294315 c.186G>A p.T62T Substitution - coding silent 17:7208213-7208213 - TCGA-43-5668-01 COSM707416 c.1677A>T p.R559R Substitution - coding silent 17:7193710-7193710 - 2492730 COSM5728221 c.189C>T p.P63P Substitution - coding silent 17:7208210-7208210 - CSCC-11-T COSM4460122 c.1153C>T p.L385L Substitution - coding silent 17:7196816-7196816 - T3152 COSM4698160 c.796G>A p.V266M Substitution - Missense 17:18234354-18234354 + TCGA-G4-6320-01 COSM5177381 c.1129G>A p.E377K Substitution - Missense 17:7196840-7196840 - HCC64 COSM1610700 c.53C>T p.P18L Substitution - Missense 17:7218606-7218606 - ESCC_BICR_023T COSM5436391 c.748C>T p.Q250* Substitution - Nonsense 17:7203216-7203216 - TCGA-AA-3715-01 COSM269498 c.980G>A p.R327Q Substitution - Missense 17:18234913-18234913 + PET052T COSM5824891 c.1264C>A p.Q422K Substitution - Missense 17:18235292-18235292 + STC291 COSM5055282 c.1299T>G p.T433T Substitution - coding silent 17:18235484-18235484 + LUAD-NYU259 COSM371787 c.1232G>C p.R411P Substitution - Missense 17:18235260-18235260 + TCGA-A3-3363-01 COSM312537 c.376G>T p.G126C Substitution - Missense 17:18232786-18232786 + LUAD-RT-S01818 COSM383891 c.1528G>A p.D510N Substitution - Missense 17:7194398-7194398 - 2492702 COSM5715501 c.2499C>A p.F833L Substitution - Missense 17:18240870-18240870 + PTC-7C COSM1563388 c.442A>G p.S148G Substitution - Missense 17:18233827-18233827 + HCC1187 COSM28351 c.1566C>G p.L522L Substitution - coding silent 17:18236894-18236894 + TCGA-B5-A11E-01 COSM983794 c.396T>C p.G132G Substitution - coding silent 17:7203760-7203760 - CHC051T COSM3667961 c.1293C>T p.P431P Substitution - coding silent 17:18235478-18235478 + TCGA-B0-5400-01 COSM473292 c.201C>A p.H67Q Substitution - Missense 17:7208198-7208198 - TCGA-DI-A0WH-01 COSM983776 c.1644+2T>C p.? Unknown 17:7193962-7193962 - TCGA-CG-5733-01 COSM4064487 c.1016G>A p.R339H Substitution - Missense 17:18234949-18234949 + TCGA-D1-A15X-01 COSM983780 c.1004G>A p.R335Q Substitution - Missense 17:7196965-7196965 - TCGA-DA-A1I7-06 COSM3514903 c.1805C>T p.T602I Substitution - Missense 17:18237674-18237674 + 23T COSM3712433 c.705A>G p.T235T Substitution - coding silent 17:7203259-7203259 - TCGA-DT-5265-01 COSM5077298 c.1529A>G p.D510G Substitution - Missense 17:7194397-7194397 - TCGA-B5-A11E-01 COSM976238 c.882T>G p.I294M Substitution - Missense 17:18234680-18234680 + HCT8 COSM4623492 c.1769G>A p.R590H Substitution - Missense 17:18237638-18237638 + TCGA-BS-A0UF-01 COSM983800 c.256G>T p.D86Y Substitution - Missense 17:7204222-7204222 - RH18C COSM2740858 c.2318C>T p.A773V Substitution - Missense 17:18240689-18240689 + TCGA-A7-A26J-01 COSM3818971 c.3155C>A p.A1052E Substitution - Missense 17:18242781-18242781 + TCGA-EE-A2MD-06 COSM3514902 c.1725C>T p.S575S Substitution - coding silent 17:18237594-18237594 + RKO COSM4648003 c.2245T>C p.S749P Substitution - Missense 17:18240616-18240616 + MO_1040 COSM5562312 c.1148C>T p.P383L Substitution - Missense 17:18235176-18235176 + TCGA-BR-4292-01 COSM4064491 c.1778T>C p.V593A Substitution - Missense 17:18237647-18237647 + TCGA-32-4208-01 COSM3403175 c.1274C>T p.A425V Substitution - Missense 17:7196514-7196514 - CSCC-29-T COSM4567617 c.78_79CC>TT p.L27F Substitution - Missense 17:7218580-7218581 - TCGA-A6-5665-01 COSM1381312 c.1299_1300insG p.R436fs*18 Insertion - Frameshift 17:18235484-18235485 + TCGA-HU-A4GN-01 COSM4064495 c.2835G>T p.P945P Substitution - coding silent 17:18241952-18241952 + TCGA-AA-3710-01 COSM5104928 c.537C>T p.G179G Substitution - coding silent 17:18233922-18233922 + KYSE-140 COSM4439497 c.1277G>A p.G426D Substitution - Missense 17:7196511-7196511 - 8033414 COSM3388121 c.2205G>C p.V735V Substitution - coding silent 17:7190807-7190807 - TCGA-EE-A20C-06 COSM3521555 c.2067C>T p.I689I Substitution - coding silent 17:7191931-7191931 - YUROG COSM5387185 c.1409C>T p.P470L Substitution - Missense 17:7196241-7196241 - TCGA-18-3407-01 COSM707418 c.2253C>T p.I751I Substitution - coding silent 17:7190759-7190759 - HCC16 COSM1609920 c.2371G>T p.V791L Substitution - Missense 17:18240742-18240742 + WSU-HN13 COSM4591668 c.1556T>G p.V519G Substitution - Missense 17:7194370-7194370 - TCGA-CM-5868-01 COSM5158622 c.127G>T p.D43Y Substitution - Missense 17:18229986-18229986 + BHY COSM2740828 c.230C>G p.T77S Substitution - Missense 17:18232545-18232545 + TCGA-AA-A00N-01 COSM274795 c.652G>A p.A218T Substitution - Missense 17:7203312-7203312 - ZZUFHECRKL-G005T COSM5435251 c.1392G>A p.A464A Substitution - coding silent 17:7196258-7196258 - 12T COSM110168 c.358C>T p.Q120* Substitution - Nonsense 17:18232768-18232768 + TCGA-CG-5733-01 COSM4064485 c.155G>A p.G52D Substitution - Missense 17:18230014-18230014 + sysucc-880T COSM5462691 c.2086C>T p.R696C Substitution - Missense 17:7191912-7191912 - 2334192 COSM312537 c.376G>T p.G126C Substitution - Missense 17:18232786-18232786 + TCGA-CH-5739-01 COSM3672552 c.900C>A p.P300P Substitution - coding silent 17:7202919-7202919 - TCGA-FS-A4FC-06 COSM3521561 c.998C>T p.S333F Substitution - Missense 17:7196971-7196971 - 08-P8005 COSM4580046 c.1062G>A p.P354P Substitution - coding silent 17:7196907-7196907 - TCGA-CG-4305-01 COSM4064488 c.1534G>A p.D512N Substitution - Missense 17:18236862-18236862 + TCGA-B5-A11E-01 COSM983798 c.267A>C p.E89D Substitution - Missense 17:7204211-7204211 - CSCC-17-T COSM4539436 c.2687G>A p.R896Q Substitution - Missense 17:18241635-18241635 + 18 COSM5745324 c.553G>A p.V185M Substitution - Missense 17:18234014-18234014 + TCGA-AP-A0LM-01 COSM983792 c.400G>A p.D134N Substitution - Missense 17:7203756-7203756 - TCGA-EE-A29V-06 COSM3514905 c.2286A>G p.A762A Substitution - coding silent 17:18240657-18240657 + T4 COSM3766166 c.1296C>T p.I432I Substitution - coding silent 17:7196492-7196492 - pfg157T COSM4750623 c.1749G>A p.W583* Substitution - Nonsense 17:18237618-18237618 + TCGA-AP-A051-01 COSM983790 c.405A>G p.P135P Substitution - coding silent 17:7203751-7203751 - 585260 COSM321407 c.455C>T p.A152V Substitution - Missense 17:18233840-18233840 + SW48 COSM2740866 c.2741C>T p.S914L Substitution - Missense 17:18241689-18241689 + TCGA-AG-A002-01 COSM260439 c.1768G>A p.A590T Substitution - Missense 17:7193537-7193537 - TCGA-AP-A0LM-01 COSM983814 c.28T>C p.S10P Substitution - Missense 17:7218631-7218631 - CSCC-16-T COSM4476029 c.2035C>T p.R679W Substitution - Missense 17:7191963-7191963 - sysucc-1972T COSM5480389 c.1506+3G>A p.? Unknown 17:18236763-18236763 + PT22_1 COSM5902387 c.1016C>T p.P339L Substitution - Missense 17:7196953-7196953 - CSCC-31-T COSM4466474 c.1437C>T p.F479F Substitution - coding silent 17:18236691-18236691 + TCGA-AX-A0J1-01 COSM976248 c.2737G>A p.A913T Substitution - Missense 17:18241685-18241685 + C467 COSM983780 c.1004G>A p.R335Q Substitution - Missense 17:7196965-7196965 - 61 COSM5740900 c.3143T>A p.L1048Q Substitution - Missense 17:18242769-18242769 + TCGA-D3-A1Q4-06 COSM3521557 c.1833G>A p.R611R Substitution - coding silent 17:7193107-7193107 - I2L-P19Tb-Tumor-Biopsy COSM5364111 c.2261T>C p.L754P Substitution - Missense 17:7190751-7190751 - TCGA-D1-A15X-01 COSM983772 c.1710G>A p.T570T Substitution - coding silent 17:7193677-7193677 - Pat_60_A COSM5851963 c.1380G>A p.W460* Substitution - Nonsense 17:18236634-18236634 + 8047893 COSM3387732 c.179+1G>A p.? Unknown 17:18230039-18230039 + TCGA-D1-A167-01 COSM983770 c.2141G>A p.R714H Substitution - Missense 17:7191323-7191323 - CHC205T COSM3766166 c.1296C>T p.I432I Substitution - coding silent 17:7196492-7196492 - TCGA-23-1031-01 COSM117029 c.1676G>A p.R559Q Substitution - Missense 17:7193711-7193711 - TCGA-E2-A1IN-01 COSM1479937 c.1003C>T p.R335W Substitution - Missense 17:7196966-7196966 - PCSI_0083_Pa_X COSM5420448 c.280-7C>T p.? Unknown 17:7204074-7204074 - HN_00076 COSM124123 c.1296C>G p.I432M Substitution - Missense 17:18235481-18235481 + SNU-175 COSM2740838 c.1242C>T p.S414S Substitution - coding silent 17:18235270-18235270 + RK107_C01 COSM1630071 c.915T>C p.F305F Substitution - coding silent 17:18234848-18234848 + Pat_74_A COSM5851962 c.959G>A p.R320H Substitution - Missense 17:18234892-18234892 + CHC205T COSM3766164 c.1575C>T p.T525T Substitution - coding silent 17:7194351-7194351 - TCGA-19-2631-01 COSM2156406 c.1214C>G p.P405R Substitution - Missense 17:18235242-18235242 + C086 COSM5533848 c.398C>T p.P133L Substitution - Missense 17:18233783-18233783 + OSCC-GB_00360111 COSM3718520 c.2345T>G p.V782G Substitution - Missense 17:18240716-18240716 + TCGA-HC-7213-01 COSM1470957 c.1881G>A p.S627S Substitution - coding silent 17:7193059-7193059 - 3N43-VS-3T43 COSM4982040 c.51C>T p.P17P Substitution - coding silent 17:7218608-7218608 - TCGA-AA-3713-01 COSM5106113 c.3117-4G>A p.? Unknown 17:18242739-18242739 + YUOTHO COSM5385816 c.1325C>T p.P442L Substitution - Missense 17:18235510-18235510 + CSCC-11-T COSM4479010 c.2289C>T p.A763A Substitution - coding silent 17:7190723-7190723 - TCGA-EE-A2MI-06 COSM3521565 c.715G>A p.E239K Substitution - Missense 17:7203249-7203249 - T3080 COSM4677777 c.1395C>A p.S465S Substitution - coding silent 17:7196255-7196255 - T3262 COSM4677773 c.1914G>A p.A638A Substitution - coding silent 17:7193026-7193026 - TCGA-B5-A11E-01 COSM983786 c.672G>A p.Q224Q Substitution - coding silent 17:7203292-7203292 - T2269 COSM4677775 c.1845G>T p.E615D Substitution - Missense 17:7193095-7193095 - T2225 COSM2740854 c.2159C>T p.S720L Substitution - Missense 17:18238562-18238562 + TCGA-D5-6540-01 COSM1385925 c.74delC p.P25fs*57 Deletion - Frameshift 17:7218585-7218585 - Gp5D COSM2740824 c.97T>C p.F33L Substitution - Missense 17:18229956-18229956 + T3021 COSM4677781 c.605T>C p.M202T Substitution - Missense 17:7203453-7203453 - CCRF-CEM COSM1679629 c.1955G>A p.R652Q Substitution - Missense 17:18238117-18238117 + 18195 COSM5346257 c.3134A>T p.E1045V Substitution - Missense 17:18242760-18242760 + T3610 COSM707417 c.2013C>T p.L671L Substitution - coding silent 17:7191985-7191985 - CSCC-60-T COSM4569239 c.1610T>C p.V537A Substitution - Missense 17:7193998-7193998 - sysucc-311T COSM5477007 c.1345G>A p.D449N Substitution - Missense 17:7196305-7196305 - PT38 COSM5923199 c.635-8C>T p.? Unknown 17:7203337-7203337 - TCGA-HF-7132-01 COSM1679629 c.1955G>A p.R652Q Substitution - Missense 17:18238117-18238117 + TCGA-EP-A12J-01 COSM4926576 c.1433C>T p.A478V Substitution - Missense 17:7194493-7194493 - TCGA-06-6694-01 COSM3402647 c.218G>A p.R73Q Substitution - Missense 17:18232533-18232533 + HCC125T COSM1610697 c.206C>T p.P69L Substitution - Missense 17:7208193-7208193 - 587384 COSM1203717 c.465G>T p.R155S Substitution - Missense 17:7203593-7203593 - TCGA-29-2429-01 COSM1324127 c.1408C>T p.L470F Substitution - Missense 17:18236662-18236662 + TCGA-CW-6087-01 COSM472384 c.2650C>T p.L884L Substitution - coding silent 17:18241598-18241598 + 19M COSM5578880 c.1819C>T p.H607Y Substitution - Missense 17:18237688-18237688 + CSCC-7-T COSM4568999 c.1436T>G p.L479R Substitution - Missense 17:7194490-7194490 - 022T COSM1728014 c.1540T>A p.W514R Substitution - Missense 17:7194386-7194386 - TCGA-EB-A24D-01 COSM3521569 c.407C>T p.S136F Substitution - Missense 17:7203749-7203749 - TCGA-CF-A3MI-01 COSM1303278 c.2221G>A p.E741K Substitution - Missense 17:7190791-7190791 - 61 COSM5740834 c.1813T>C p.C605R Substitution - Missense 17:7193492-7193492 - CSCC-20-T COSM4481844 c.2549C>T p.T850M Substitution - Missense 17:18241497-18241497 + TCGA-D3-A3C3-06 COSM3514899 c.819G>A p.T273T Substitution - coding silent 17:18234377-18234377 + T613 COSM4677779 c.1092G>A p.T364T Substitution - coding silent 17:7196877-7196877 - TCGA-AP-A051-01 COSM983788 c.507C>T p.R169R Substitution - coding silent 17:7203551-7203551 - TCGA-CG-5722-01 COSM4069175 c.498G>A p.V166V Substitution - coding silent 17:7203560-7203560 - 234 COSM3730552 c.681G>A p.S227S Substitution - coding silent 17:18234142-18234142 + HCC8 COSM1609919 c.535G>A p.G179S Substitution - Missense 17:18233920-18233920 + TCGA-AP-A0LM-01 COSM983774 c.1701G>T p.E567D Substitution - Missense 17:7193686-7193686 - sysucc-1370T COSM4851523 c.2170C>T p.R724C Substitution - Missense 17:18238573-18238573 + TCGA-AP-A056-01 COSM983778 c.1067G>A p.R356Q Substitution - Missense 17:7196902-7196902 - LUAD-S01302 COSM395651 c.904G>A p.D302N Substitution - Missense 17:7202915-7202915 - HCC1187 COSM28351 c.1566C>G p.L522L Substitution - coding silent 17:18236894-18236894 + TCGA-D1-A17Q-01 COSM983796 c.295G>A p.G99R Substitution - Missense 17:7204052-7204052 - PD4076a COSM5798952 c.501C>T p.D167D Substitution - coding silent 17:7203557-7203557 - CSCC-18-T COSM4513459 c.939C>T p.P313P Substitution - coding silent 17:18234872-18234872 + C008 COSM5523023 c.1496C>T p.P499L Substitution - Missense 17:18236750-18236750 + CSCC-29-T COSM3937277 c.1501C>T p.R501C Substitution - Missense 17:18236755-18236755 + TCGA-B5-A11U-01 COSM976258 c.3172G>A p.A1058T Substitution - Missense 17:18242798-18242798 + YUGATOR COSM5385817 c.2196C>T p.F732F Substitution - coding silent 17:18238599-18238599 + ESCC-190T COSM3937539 c.1108A>T p.I370F Substitution - Missense 17:7196861-7196861 - PD11745a COSM5796198 c.1329C>T p.F443F Substitution - coding silent 17:7196321-7196321 - TCGA-B5-A0JY-01 COSM976246 c.2482G>A p.A828T Substitution - Missense 17:18240853-18240853 + MZ7-mel COSM28352 c.850+1G>A p.? Unknown 17:18234409-18234409 + 587284 COSM1213450 c.2662C>A p.H888N Substitution - Missense 17:18241610-18241610 + TCGA-AP-A054-01 COSM976240 c.1513T>A p.C505S Substitution - Missense 17:18236841-18236841 + TCGA-EE-A2MS-06 COSM3521567 c.426C>T p.I142I Substitution - coding silent 17:7203730-7203730 - HCC125 COSM1610697 c.206C>T p.P69L Substitution - Missense 17:7208193-7208193 - LUAD-RT-S01700 COSM378684 c.1492C>T p.R498C Substitution - Missense 17:7194434-7194434 - CHC051T COSM3667961 c.1293C>T p.P431P Substitution - coding silent 17:18235478-18235478 + TCGA-CM-4743-01 COSM1381314 c.2329G>A p.V777M Substitution - Missense 17:18240700-18240700 + TCGA-GC-A3RC-01 COSM3796023 c.2295G>C p.E765D Substitution - Missense 17:7190717-7190717 - TCGA-A8-A07E-01 COSM5833244 c.1480_1482delGAG p.E494delE Deletion - In frame 17:18236734-18236736 + TCGA-AA-3492-01 COSM1381315 c.2713C>T p.R905W Substitution - Missense 17:18241661-18241661 + TCGA-AA-3510-01 COSM1385896 c.423G>T p.K141N Substitution - Missense 17:7203733-7203733 - CSCC-49-T COSM4474553 c.1929C>T p.S643S Substitution - coding silent 17:18238091-18238091 + TCGA-D1-A103-01 COSM976244 c.2171G>A p.R724H Substitution - Missense 17:18238574-18238574 + 1342576 COSM51326 c.191C>T p.P64L Substitution - Missense 17:7208208-7208208 - TCGA-DK-A2I6-01 COSM1303281 c.149C>G p.S50* Substitution - Nonsense 17:7218251-7218251 - HCC8T COSM1609919 c.535G>A p.G179S Substitution - Missense 17:18233920-18233920 + ESCC-139T COSM3937537 c.1218C>T p.N406N Substitution - coding silent 17:7196570-7196570 - T3225 COSM4698161 c.1502G>A p.R501H Substitution - Missense 17:18236756-18236756 + YUGATOR COSM5387188 c.327C>T p.I109I Substitution - coding silent 17:7204020-7204020 - SNUH_G45_S1 COSM3766166 c.1296C>T p.I432I Substitution - coding silent 17:7196492-7196492 - TCGA-CA-6717-01 COSM1385822 c.2254G>A p.E752K Substitution - Missense 17:7190758-7190758 - Pat_41_B COSM5853367 c.164A>G p.Y55C Substitution - Missense 17:7208235-7208235 - TCGA-CA-6717-01 COSM1385855 c.1802A>G p.K601R Substitution - Missense 17:7193503-7193503 - LUAD-NYU1051S COSM368641 c.1155A>T p.P385P Substitution - coding silent 17:18235183-18235183 + CSCC-27-T COSM4472510 c.1788C>T p.S596S Substitution - coding silent 17:7193517-7193517 - PT23_1 COSM5903136 c.2269C>T p.P757S Substitution - Missense 17:7190743-7190743 - TCGA-FS-A1ZS-06 COSM3514901 c.1395G>A p.V465V Substitution - coding silent 17:18236649-18236649 + 2492701 COSM5715501 c.2499C>A p.F833L Substitution - Missense 17:18240870-18240870 + ESO-859 COSM1239335 c.2947C>A p.P983T Substitution - Missense 17:18242230-18242230 + HX14T COSM1609919 c.535G>A p.G179S Substitution - Missense 17:18233920-18233920 + TCGA-AC-A23H-01 COSM3820426 c.1740C>T p.I580I Substitution - coding silent 17:7193565-7193565 - UM-SCC-2 COSM4591668 c.1556T>G p.V519G Substitution - Missense 17:7194370-7194370 - TCGA-GF-A6C9-06 COSM3521555 c.2067C>T p.I689I Substitution - coding silent 17:7191931-7191931 - TCGA-19-2631 COSM2156406 c.1214C>G p.P405R Substitution - Missense 17:18235242-18235242 + TCGA-CG-5721-01 COSM260439 c.1768G>A p.A590T Substitution - Missense 17:7193537-7193537 - TCGA-D9-A6EC-06 COSM4401173 c.1657A>T p.S553C Substitution - Missense 17:18237526-18237526 + 2334199 COSM319905 c.1190G>T p.R397L Substitution - Missense 17:7196779-7196779 - TCGA-CM-4744-01 COSM1385847 c.1862G>A p.R621Q Substitution - Missense 17:7193078-7193078 - TCGA-BF-A1Q0-01 COSM3521571 c.403C>T p.P135S Substitution - Missense 17:7203753-7203753 - 93VU147T COSM4591668 c.1556T>G p.V519G Substitution - Missense 17:7194370-7194370 - H1672 COSM312537 c.376G>T p.G126C Substitution - Missense 17:18232786-18232786 + TCGA-EE-A3AE-06 COSM3521563 c.719G>A p.G240E Substitution - Missense 17:7203245-7203245 - ESCC_64 COSM5633472 c.204C>A p.S68R Substitution - Missense 17:7208195-7208195 - TCGA-BR-8591-01 COSM4064492 c.1800T>A p.A600A Substitution - coding silent 17:18237669-18237669 + TCGA-EE-A3JD-06 COSM4396605 c.1205C>T p.A402V Substitution - Missense 17:18235233-18235233 + DLD1 COSM4623492 c.1769G>A p.R590H Substitution - Missense 17:18237638-18237638 + TCGA-BR-6452-01 COSM4064493 c.2224A>G p.T742A Substitution - Missense 17:18240595-18240595 + EGC15 COSM5055283 c.2659G>A p.V887I Substitution - Missense 17:18241607-18241607 + TCGA-AM-5821-01 COSM3691404 c.1947G>A p.P649P Substitution - coding silent 17:18238109-18238109 + TCGA-DI-A0WH-01 COSM976236 c.647G>A p.S216N Substitution - Missense 17:18234108-18234108 + TCGA-G4-6311-01 COSM3691763 c.1773C>T p.N591N Substitution - coding silent 17:7193532-7193532 - CCRF-CEM COSM1679628 c.569G>A p.R190H Substitution - Missense 17:18234030-18234030 + SUNE1 COSM2740867 c.2753C>T p.T918M Substitution - Missense 17:18241701-18241701 + TCGA-59-2352-01 COSM70457 c.1163G>A p.G388D Substitution - Missense 17:7196806-7196806 - TCGA-D9-A1JW-06 COSM3889391 c.598T>G p.S200A Substitution - Missense 17:18234059-18234059 + TCGA-EK-A3GK-01 COSM4853101 c.1685C>G p.S562W Substitution - Missense 17:7193702-7193702 - C0011T COSM4151734 c.1846T>A p.Y616N Substitution - Missense 17:7193094-7193094 - TCGA-IR-A3LK-01 COSM4816652 c.955G>A p.D319N Substitution - Missense 17:18234888-18234888 + CSCC-11-T COSM4514568 c.979C>T p.R327* Substitution - Nonsense 17:18234912-18234912 + 2492703 COSM5715501 c.2499C>A p.F833L Substitution - Missense 17:18240870-18240870 + OSCC-GB_00640111 COSM4885240 c.1886G>A p.R629Q Substitution - Missense 17:7193054-7193054 - HCT15 COSM4623492 c.1769G>A p.R590H Substitution - Missense 17:18237638-18237638 + TCGA-EE-A181-06 COSM3521553 c.2084C>T p.P695L Substitution - Missense 17:7191914-7191914 - C0072T COSM4151736 c.1519G>T p.D507Y Substitution - Missense 17:7194407-7194407 - HCC154T COSM5807228 c.1789G>A p.E597K Substitution - Missense 17:7193516-7193516 - TCGA-AP-A051-01 COSM976250 c.2742G>A p.S914S Substitution - coding silent 17:18241690-18241690 + STC252 COSM5055735 c.538C>A p.L180I Substitution - Missense 17:7203520-7203520 - TCGA-A5-A0VP-01 COSM976242 c.1982G>A p.R661H Substitution - Missense 17:18238144-18238144 + TCGA-BS-A0UF-01 COSM983784 c.714C>T p.I238I Substitution - coding silent 17:7203250-7203250 - Pat_66_A COSM5853363 c.2021C>T p.S674L Substitution - Missense 17:7191977-7191977 - TCGA-FW-A3R5-06 COSM3890299 c.1206C>T p.I402I Substitution - coding silent 17:7196763-7196763 - H1155 COSM1195347 c.1657A>G p.S553G Substitution - Missense 17:18237526-18237526 + BCM399T COSM2740858 c.2318C>T p.A773V Substitution - Missense 17:18240689-18240689 + TCGA-CA-6717-01 COSM983778 c.1067G>A p.R356Q Substitution - Missense 17:7196902-7196902 - SJDES001-R COSM4580044 c.1479G>C p.Q493H Substitution - Missense 17:7194447-7194447 - I2L-P19Ta-Tumor-Organoid COSM5364071 c.2979C>A p.A993A Substitution - coding silent 17:18242262-18242262 + TCGA-BR-4292-01 COSM4064490 c.1713C>T p.H571H Substitution - coding silent 17:18237582-18237582 + TCGA-F1-6874-01 COSM4064494 c.2665G>A p.V889I Substitution - Missense 17:18241613-18241613 + TCGA-BG-A0VV-01 COSM976254 c.2756G>A p.R919H Substitution - Missense 17:18241704-18241704 + HCC16T COSM1609920 c.2371G>T p.V791L Substitution - Missense 17:18240742-18240742 + TCGA-NH-A6GB-01 COSM5184938 c.3180C>T p.A1060A Substitution - coding silent 17:18242806-18242806 + TCGA-EE-A2MI-06 COSM3514904 c.2223C>T p.P741P Substitution - coding silent 17:18240594-18240594 + MO_1162 COSM5552928 c.508G>T p.E170* Substitution - Nonsense 17:7203550-7203550 - ESCC_157 COSM5646288 c.1015C>G p.P339A Substitution - Missense 17:7196954-7196954 - TCGA-CJ-6033-01 COSM472382 c.255C>T p.T85T Substitution - coding silent 17:18232570-18232570 + TCGA-B5-A11Y-01 COSM976252 c.2745C>T p.C915C Substitution - coding silent 17:18241693-18241693 + TCGA-FW-A3TV-06 COSM3521559 c.1634T>G p.L545* Substitution - Nonsense 17:7193974-7193974 - HCA7 COSM976246 c.2482G>A p.A828T Substitution - Missense 17:18240853-18240853 + TCGA-DM-A28A-01 COSM5170321 c.129C>A p.D43E Substitution - Missense 17:7218271-7218271 - OSCC-GB_00230111 COSM3712433 c.705A>G p.T235T Substitution - coding silent 17:7203259-7203259 - TCGA-CZ-4857-01 COSM3773774 c.359A>G p.Q120R Substitution - Missense 17:18232769-18232769 + TCGA-C8-A12U-01 COSM436150 c.3115G>C p.G1039R Substitution - Missense 17:18242627-18242627 + WA16 COSM240495 c.538G>A p.E180K Substitution - Missense 17:18233923-18233923 + UM-SCC-17B COSM4591668 c.1556T>G p.V519G Substitution - Missense 17:7194370-7194370 - tumor_4160100 COSM5949284 c.742G>A p.D248N Substitution - Missense 17:18234300-18234300 + 587278 COSM1213449 c.115G>A p.A39T Substitution - Missense 17:18229974-18229974 + WSU-HN30 COSM4600736 c.1531G>T p.E511* Substitution - Nonsense 17:7194395-7194395 - TCGA-AA-A00N-01 COSM274796 c.394G>A p.G132S Substitution - Missense 17:7203762-7203762 - TCGA-BR-8487-01 COSM4064486 c.364C>T p.P122S Substitution - Missense 17:18232774-18232774 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.463838;Hs.463844;Hs.463864;Hs.463890;Hs.463900;Hs.463928 17p13.1 602887 Hs.513983 17p11.2 600966

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AG - IntronicDeletion . c.159+1105_159+1106delCT 17 7120454 UCEC A G Missense p.Y623H c.1867T>C 17 7096392 STAD A - IntronicDeletion . c.2106-107delT 17 7094784 CM C A Missense p.R397L c.1190G>T 17 7100098 SCLC C G Missense p.G376R c.1126G>C 17 7100162 LUSC C G Missense p.R9S c.27G>C 17 7121951 GBM CTGCAGAGAGAGCC - SpliceAcceptorDeletion . c.1721-14_1721-1delGGCTCTCTCTGCAG 17 7096904 CM C T Missense p.D483N c.1447G>A 17 7097798 LUAD C T Missense p.D592N c.1774G>A 17 7096850 CM C T Missense p.E239K c.715G>A 17 7106568 CM C T Missense p.E741K c.2221G>A 17 7094110 BLCA C T Missense p.G240E c.719G>A 17 7106564 CM C T Missense p.G388D c.1163G>A 17 7100125 OV C T Missense p.G620D c.1859G>A 17 7096400 STAD C T Missense p.R559Q c.1676G>A 17 7097030 OV C T Missense p.R694H c.2081G>A 17 7095236 STAD C T SpliceAcceptorSNV . c.635-1G>A 17 7106649 STAD C T Synonymous p.R611R c.1833G>A 17 7096426 CM C T Synonymous p.S627S c.1881G>A 17 7096378 PRAD C T Synonymous p.V166V c.498G>A 17 7106879 STAD G A Missense p.A425V c.1274C>T 17 7099833 GBM G A Missense p.P64S c.190C>T 17 7111528 CM G A Missense p.R335W c.1003C>T 17 7100285 BRCA G A Missense p.S136F c.407C>T 17 7107068 CM G A Missense p.S333F c.998C>T 17 7100290 CM G A Synonymous p.F474F c.1422C>T 17 7099547 HNSC G A Synonymous p.I142I c.426C>T 17 7107049 CM G A Synonymous p.I689I c.2067C>T 17 7095250 CM G A Synonymous p.I751I c.2253C>T 17 7094078 LUSC G A Synonymous p.L671L c.2013C>T 17 7095304 LUSC G A Synonymous p.P695P c.2085C>T 17 7095232 LUAD G C Nonsense p.S50* c.149C>G 17 7121570 BLCA G C Synonymous p.R694R c.2082C>G 17 7095235 LUAD GG AA Missense p.P135L c.403_404delinsTT 17 7107071 CM GG AA Missense p.P695L c.2084_2085delinsTT 17 7095232 CM - G IntronicInsertion . c.916+103dupC 17 7106119 STAD G T Missense p.H67Q c.201C>A 17 7111517 RCCC G T Missense p.L321M c.961C>A 17 7100327 UCEC T A Missense p.Q493L c.1478A>T 17 7097767 LUAD T A Synonymous p.R559R c.1677A>T 17 7097029 LUSC T G Missense p.K208Q c.622A>C 17 7106755 LGG - A Frameshift p.L685Vfs*10 c.2051dupA 17 18141526 RCCC A G Missense p.Q120R c.359A>G 17 18136083 RCCC A G Synonymous p.A1007A c.3021A>G 17 18145847 CM A G Synonymous p.A762A c.2286A>G 17 18143971 CM C A Missense p.L94I c.280C>A 17 18136004 LUSC C A Missense p.P983T c.2947C>A 17 18145544 ESCA C A Synonymous p.A410A c.1230C>A 17 18138572 OV C G Missense p.I432M c.1296C>G 17 18138795 HNSC C G Missense p.P405R c.1214C>G 17 18138556 GBM C T IntronicSNV . c.1352+35C>T 17 18138886 CM C T Missense p.A152V c.455C>T 17 18137154 SCLC C T Missense p.A402V c.1205C>T 17 18138547 CM C T Missense p.P34L c.101C>T 17 18133274 CM C T Missense p.R183C c.547C>T 17 18137246 RCCC C T Missense p.R709C c.2125C>T 17 18141842 CM C T Missense p.R955C c.2863C>T 17 18145294 CLL C T Missense p.S255L c.764C>T 17 18137636 BLCA C T Missense p.T602I c.1805C>T 17 18140988 CM C T Missense p.T918M c.2753C>T 17 18145015 LGG C T Synonymous p.C915C c.2745C>T 17 18145007 UCEC C T Synonymous p.D187D c.561C>T 17 18137336 PRAD C T Synonymous p.F587F c.1761C>T 17 18140944 CM C T Synonymous p.H571H c.1713C>T 17 18140896 STAD C T Synonymous p.I912I c.2736C>T 17 18144998 CM C T Synonymous p.P741P c.2223C>T 17 18143908 CM C T Synonymous p.R955R c.2865C>T 17 18145296 BRCA C T Synonymous p.S575S c.1725C>T 17 18140908 CM C T Synonymous p.S842S c.2526C>T 17 18144788 HNSC C T Synonymous p.T85T c.255C>T 17 18135884 RCCC G A IntronicSNV . c.2767+53G>A 17 18145082 CM G A Missense p.A957T c.2869G>A 17 18145300 UCEC G A Missense p.D512N c.1534G>A 17 18140176 STAD G A Missense p.E352K c.1054G>A 17 18138301 CM G A Missense p.G52D c.155G>A 17 18133328 STAD G A Missense p.R339H c.1016G>A 17 18138263 STAD G A Missense p.R73Q c.218G>A 17 18135847 GBM G A Missense p.R919H c.2756G>A 17 18145018 UCEC G A Missense p.S216N c.647G>A 17 18137422 UCEC G A Missense p.V540I c.1618G>A 17 18140801 STAD G A Missense p.V889I c.2665G>A 17 18144927 STAD G A Synonymous p.T273T c.819G>A 17 18137691 CM G A Synonymous p.V465V c.1395G>A 17 18139963 CM G C Missense p.G1039R c.3115G>C 17 18145941 BRCA G C Synonymous p.G579G c.1737G>C 17 18140920 CM G C Synonymous p.R940R c.2820G>C 17 18145251 LUAD G T Missense p.G126C c.376G>T 17 18136100 SCLC G T Missense p.G56V c.167G>T 17 18133340 LUAD T A IntronicSNV . c.1353-156T>A 17 18139765 CM T A Missense p.C505S c.1513T>A 17 18140155 UCEC T C Missense p.V593A c.1778T>C 17 18140961 STAD T C Synonymous p.F305F c.915T>C 17 18138162 HC T G Missense p.S200A c.598T>G 17 18137373 CM