Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 19 10600462 10600462 + Missense_Mutation SNP C C T TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chr19:10600462C>T c.1393G>A c.(1393-1395)Gtg>Atg p.V465M BLCA 19 10597496 10597496 + Splice_Site SNP T T C TCGA-CU-A0YR-01A-12D-A10S-08 TCGA-CU-A0YR-10A-01D-A10S-08 g.chr19:10597496T>C c.e6-2 BLCA 19 10599872 10599872 + Silent SNP G G A TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr19:10599872G>A c.1704C>T c.(1702-1704)gtC>gtT p.V568V BLCA 19 10599968 10599969 + Frame_Shift_Ins INS - - CA TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr19:10599968_10599969insCA c.1607_1608insTG c.(1606-1608)cgcfs p.R536fs BLCA 19 10600444 10600444 + Missense_Mutation SNP G G A TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr19:10600444G>A c.1411C>T c.(1411-1413)Ctc>Ttc p.L471F BLCA 19 10602447 10602447 + Silent SNP C C T TCGA-ZF-AA4N-01A-11D-A38G-08 TCGA-ZF-AA4N-10A-01D-A38J-08 g.chr19:10602447C>T c.1131G>A c.(1129-1131)gtG>gtA p.V377V BLCA 19 10602630 10602630 + Silent SNP C C T TCGA-G2-A2EJ-01A-11D-A17V-08 TCGA-G2-A2EJ-10A-01D-A17V-08 g.chr19:10602630C>T c.948G>A c.(946-948)gtG>gtA p.V316V BLCA 19 10602630 10602630 + Silent SNP C C T TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr19:10602630C>T c.948G>A c.(946-948)gtG>gtA p.V316V BLCA 19 10602848 10602848 + Missense_Mutation SNP C C T TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr19:10602848C>T c.730G>A c.(730-732)Gag>Aag p.E244K BLCA 19 10602872 10602872 + Missense_Mutation SNP C C T TCGA-ZF-AA4N-01A-11D-A38G-08 TCGA-ZF-AA4N-10A-01D-A38J-08 g.chr19:10602872C>T c.706G>A c.(706-708)Gac>Aac p.D236N BLCA 19 10602915 10602915 + Silent SNP G G A TCGA-4Z-AA84-01A-11D-A391-08 TCGA-4Z-AA84-10A-01D-A394-08 g.chr19:10602915G>A c.663C>T c.(661-663)ttC>ttT p.F221F BLCA 19 10602926 10602926 + Missense_Mutation SNP C C G TCGA-G2-A2EJ-01A-11D-A17V-08 TCGA-G2-A2EJ-10A-01D-A17V-08 g.chr19:10602926C>G c.652G>C c.(652-654)Gag>Cag p.E218Q BLCA 19 10610363 10610363 + Missense_Mutation SNP C C G TCGA-GC-A3WC-01A-31D-A22Z-08 TCGA-GC-A3WC-10A-01D-A22Z-08 g.chr19:10610363C>G c.347G>C c.(346-348)cGg>cCg p.R116P BLCA 19 10610576 10610576 + Missense_Mutation SNP G G A TCGA-GU-A42Q-01A-11D-A23U-08 TCGA-GU-A42Q-10A-01D-A23U-08 g.chr19:10610576G>A c.134C>T c.(133-135)tCc>tTc p.S45F BLCA 19 10610637 10610637 + Missense_Mutation SNP C C T TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr19:10610637C>T c.73G>A c.(73-75)Gag>Aag p.E25K BRCA 19 10600498 10600499 + Frame_Shift_Ins INS - - T TCGA-A8-A09W-01A-11W-A019-09 TCGA-A8-A09W-10A-01W-A021-09 g.chr19:10600498_10600499insT c.1356_1357insA c.(1354-1359)ttggtgfs p.V453fs BRCA 19 10600502 10600502 + Frame_Shift_Del DEL G G - TCGA-A8-A09W-01A-11W-A019-09 TCGA-A8-A09W-10A-01W-A021-09 g.chr19:10600502delG c.1353delC c.(1351-1353)cacfs p.H451fs BRCA 19 10600510 10600510 + Nonsense_Mutation SNP C C A TCGA-EW-A1J5-01A-11D-A13L-09 TCGA-EW-A1J5-10A-01D-A13O-09 g.chr19:10600510C>A c.1345G>T c.(1345-1347)Gag>Tag p.E449* BRCA 19 10610217 10610217 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr19:10610217C>T c.493G>A c.(493-495)Gac>Aac p.D165N CESC 19 10602878 10602878 + Missense_Mutation SNP G G A TCGA-JW-A5VK-01A-11D-A28B-09 TCGA-JW-A5VK-10A-01D-A28E-09 g.chr19:10602878G>A c.700C>T c.(700-702)Cgg>Tgg p.R234W CHOL 19 10602675 10602680 + In_Frame_Del DEL CAGGTA CAGGTA - TCGA-W5-AA2X-01A-11D-A417-09 TCGA-W5-AA2X-10A-01D-A41A-09 g.chr19:10602675_10602680delCAGGTA c.898_903delTACCTG c.(898-903)tacctgdel p.YL300del CHOL 19 10610426 10610426 + Missense_Mutation SNP G G A TCGA-ZH-A8Y8-01A-51D-A417-09 TCGA-ZH-A8Y8-10A-01D-A41A-09 g.chr19:10610426G>A c.284C>T c.(283-285)gCc>gTc p.A95V COAD 19 10599902 10599902 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr19:10599902C>T c.1674G>A c.(1672-1674)ggG>ggA p.G558G COAD 19 10599969 10599969 + Missense_Mutation SNP C C T TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr19:10599969C>T c.1607G>A c.(1606-1608)cGc>cAc p.R536H COAD 19 10600346 10600346 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr19:10600346C>A c.1509G>T c.(1507-1509)atG>atT p.M503I COAD 19 10610217 10610217 + Missense_Mutation SNP C C T TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr19:10610217C>T c.493G>A c.(493-495)Gac>Aac p.D165N COAD 19 10610337 10610337 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr19:10610337T>C c.373A>G c.(373-375)Att>Gtt p.I125V COAD 19 10610577 10610577 + Missense_Mutation SNP A A G TCGA-A6-4105-01A-02D-1771-10 TCGA-A6-4105-10A-01D-1771-10 g.chr19:10610577A>G c.133T>C c.(133-135)Tcc>Ccc p.S45P COAD 19 10610686 10610686 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr19:10610686G>A c.24C>T c.(22-24)agC>agT p.S8S COAD 19 10610686 10610686 + Silent SNP G G A TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr19:10610686G>A c.24C>T c.(22-24)agC>agT p.S8S COADREAD 19 10599902 10599902 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr19:10599902C>T c.1674G>A c.(1672-1674)ggG>ggA p.G558G COADREAD 19 10599969 10599969 + Missense_Mutation SNP C C T TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr19:10599969C>T c.1607G>A c.(1606-1608)cGc>cAc p.R536H COADREAD 19 10600346 10600346 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr19:10600346C>A c.1509G>T c.(1507-1509)atG>atT p.M503I COADREAD 19 10610217 10610217 + Missense_Mutation SNP C C T TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr19:10610217C>T c.493G>A c.(493-495)Gac>Aac p.D165N COADREAD 19 10610337 10610337 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr19:10610337T>C c.373A>G c.(373-375)Att>Gtt p.I125V COADREAD 19 10610577 10610577 + Missense_Mutation SNP A A G TCGA-A6-4105-01A-02D-1771-10 TCGA-A6-4105-10A-01D-1771-10 g.chr19:10610577A>G c.133T>C c.(133-135)Tcc>Ccc p.S45P COADREAD 19 10610686 10610686 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr19:10610686G>A c.24C>T c.(22-24)agC>agT p.S8S COADREAD 19 10610686 10610686 + Silent SNP G G A TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr19:10610686G>A c.24C>T c.(22-24)agC>agT p.S8S DLBC 19 10602344 10602344 + Missense_Mutation SNP G G A TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr19:10602344G>A c.1234C>T c.(1234-1236)Ccc>Tcc p.P412S ESCA 19 10602340 10602340 + Missense_Mutation SNP C C T TCGA-L5-A88Z-01A-11D-A36J-09 TCGA-L5-A88Z-11A-11D-A36M-09 g.chr19:10602340C>T c.1238G>A c.(1237-1239)cGt>cAt p.R413H ESCA 19 10602767 10602767 + Missense_Mutation SNP C C T TCGA-VR-A8EU-01A-11D-A36J-09 TCGA-VR-A8EU-10A-01D-A36M-09 g.chr19:10602767C>T c.811G>A c.(811-813)Gtg>Atg p.V271M ESCA 19 10602788 10602788 + Missense_Mutation SNP C C T TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr19:10602788C>T c.790G>A c.(790-792)Gtc>Atc p.V264I ESCA 19 10610154 10610154 + Missense_Mutation SNP C C T TCGA-LN-A4A2-01A-31D-A27G-09 TCGA-LN-A4A2-10A-01D-A27G-09 g.chr19:10610154C>T c.556G>A c.(556-558)Ggc>Agc p.G186S ESCA 19 10610187 10610187 + Missense_Mutation SNP G G C TCGA-L5-A8NT-01A-11D-A37C-09 TCGA-L5-A8NT-11A-11D-A37F-09 g.chr19:10610187G>C c.523C>G c.(523-525)Ctg>Gtg p.L175V ESCA 19 10610255 10610255 + Missense_Mutation SNP A A G TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr19:10610255A>G c.455T>C c.(454-456)gTc>gCc p.V152A ESCA 19 10610581 10610581 + Silent SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr19:10610581C>T c.129G>A c.(127-129)acG>acA p.T43T GBMLGG 19 10600040 10600040 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:10600040G>A c.1536C>T c.(1534-1536)gtC>gtT p.V512V GBMLGG 19 10602360 10602360 + Silent SNP G G A TCGA-DU-A7TA-01A-11D-A33T-08 TCGA-DU-A7TA-10A-01D-A33W-08 g.chr19:10602360G>A c.1218C>T c.(1216-1218)tgC>tgT p.C406C HNSC 19 10597384 10597384 + Missense_Mutation SNP C C G TCGA-CR-6492-01A-12D-2078-08 TCGA-CR-6492-10A-01D-2078-08 g.chr19:10597384C>G c.1819G>C c.(1819-1821)Gct>Cct p.A607P HNSC 19 10597411 10597411 + Missense_Mutation SNP T T C TCGA-BA-7269-01A-11D-2012-08 TCGA-BA-7269-10A-01D-2013-08 g.chr19:10597411T>C c.1792A>G c.(1792-1794)Aca>Gca p.T598A HNSC 19 10600002 10600002 + Missense_Mutation SNP T T C TCGA-UF-A7JF-01A-11D-A34J-08 TCGA-UF-A7JF-10A-01D-A34M-08 g.chr19:10600002T>C c.1574A>G c.(1573-1575)tAt>tGt p.Y525C HNSC 19 10600019 10600019 + Missense_Mutation SNP G G C TCGA-HD-A633-01A-11D-A28R-08 TCGA-HD-A633-10A-01D-A28U-08 g.chr19:10600019G>C c.1557C>G c.(1555-1557)atC>atG p.I519M HNSC 19 10600446 10600446 + Missense_Mutation SNP C C T TCGA-DQ-7588-01A-11D-2078-08 TCGA-DQ-7588-10B-01D-2078-08 g.chr19:10600446C>T c.1409G>A c.(1408-1410)cGt>cAt p.R470H HNSC 19 10600447 10600447 + Missense_Mutation SNP G G A TCGA-CV-5434-01A-01D-1683-08 TCGA-CV-5434-10A-01D-1870-08 g.chr19:10600447G>A c.1408C>T c.(1408-1410)Cgt>Tgt p.R470C HNSC 19 10602293 10602293 + Missense_Mutation SNP C C T TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr19:10602293C>T c.1285G>A c.(1285-1287)Ggc>Agc p.G429S HNSC 19 10602303 10602303 + Missense_Mutation SNP G G C TCGA-UF-A7JT-01A-11D-A34J-08 TCGA-UF-A7JT-10A-01D-A34M-08 g.chr19:10602303G>C c.1275C>G c.(1273-1275)atC>atG p.I425M HNSC 19 10602622 10602622 + Missense_Mutation SNP C C A TCGA-CV-7248-01A-11D-2012-08 TCGA-CV-7248-10A-01D-2013-08 g.chr19:10602622C>A c.956G>T c.(955-957)tGc>tTc p.C319F HNSC 19 10602732 10602732 + Silent SNP C C T TCGA-CN-4742-01A-02D-1512-08 TCGA-CN-4742-10A-01D-1512-08 g.chr19:10602732C>T c.846G>A c.(844-846)caG>caA p.Q282Q HNSC 19 10602745 10602745 + Missense_Mutation SNP G G A TCGA-UF-A71E-01A-31D-A34J-08 TCGA-UF-A71E-10B-01D-A34M-08 g.chr19:10602745G>A c.833C>T c.(832-834)cCg>cTg p.P278L HNSC 19 10602764 10602764 + Missense_Mutation SNP G G A TCGA-CN-5359-01A-01D-1434-08 TCGA-CN-5359-10A-01D-1434-08 g.chr19:10602764G>A c.814C>T c.(814-816)Cgc>Tgc p.R272C HNSC 19 10602863 10602863 + Missense_Mutation SNP C C T TCGA-P3-A6T0-01A-12D-A34J-08 TCGA-P3-A6T0-10A-01D-A34M-08 g.chr19:10602863C>T c.715G>A c.(715-717)Gtg>Atg p.V239M HNSC 19 10602878 10602878 + Missense_Mutation SNP G G A TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr19:10602878G>A c.700C>T c.(700-702)Cgg>Tgg p.R234W HNSC 19 10602926 10602926 + Missense_Mutation SNP C C T TCGA-T2-A6WX-01A-12D-A34J-08 TCGA-T2-A6WX-10B-01D-A34M-08 g.chr19:10602926C>T c.652G>A c.(652-654)Gag>Aag p.E218K HNSC 19 10610149 10610149 + Silent SNP G G A TCGA-CV-5970-01A-11D-1683-08 TCGA-CV-5970-10A-01D-1870-08 g.chr19:10610149G>A c.561C>T c.(559-561)atC>atT p.I187I HNSC 19 10610177 10610177 + Missense_Mutation SNP T T A TCGA-CN-6010-01A-11D-1683-08 TCGA-CN-6010-10A-01D-1683-08 g.chr19:10610177T>A c.533A>T c.(532-534)cAg>cTg p.Q178L HNSC 19 10610205 10610205 + Missense_Mutation SNP G G A TCGA-CV-7238-01A-11D-2012-08 TCGA-CV-7238-10A-01D-2013-08 g.chr19:10610205G>A c.505C>T c.(505-507)Cgt>Tgt p.R169C HNSC 19 10610277 10610277 + Missense_Mutation SNP T T A TCGA-CV-5978-01A-11D-1683-08 TCGA-CV-5978-11A-01D-1683-08 g.chr19:10610277T>A c.433A>T c.(433-435)Atc>Ttc p.I145F HNSC 19 10610310 10610310 + Nonsense_Mutation SNP C C A TCGA-UF-A7JF-01A-11D-A34J-08 TCGA-UF-A7JF-10A-01D-A34M-08 g.chr19:10610310C>A c.400G>T c.(400-402)Gag>Tag p.E134* HNSC 19 10610334 10610335 + Frame_Shift_Ins INS - - A TCGA-CV-A6JU-01A-11D-A31L-08 TCGA-CV-A6JU-10A-01D-A31J-08 g.chr19:10610334_10610335insA c.375_376insT c.(373-378)attgagfs p.E126fs HNSC 19 10610402 10610402 + Missense_Mutation SNP G G T TCGA-CN-6012-01A-11D-1683-08 TCGA-CN-6012-10A-01D-1683-08 g.chr19:10610402G>T c.308C>A c.(307-309)tCc>tAc p.S103Y HNSC 19 10610554 10610554 + Silent SNP G G A TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr19:10610554G>A c.156C>T c.(154-156)ttC>ttT p.F52F HNSC 19 10610576 10610576 + Missense_Mutation SNP G G A TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr19:10610576G>A c.134C>T c.(133-135)tCc>tTc p.S45F HNSC 19 10610576 10610576 + Missense_Mutation SNP G G T TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr19:10610576G>T c.134C>A c.(133-135)tCc>tAc p.S45Y HNSC 19 10610625 10610625 + Missense_Mutation SNP C C G TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr19:10610625C>G c.85G>C c.(85-87)Gac>Cac p.D29H HNSC 19 10610642 10610642 + Missense_Mutation SNP C C T TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr19:10610642C>T c.68G>A c.(67-69)tGc>tAc p.C23Y KIPAN 19 10599946 10599946 + Missense_Mutation SNP A A G TCGA-B0-4815-01A-01D-1501-10 TCGA-B0-4815-11A-02D-1501-10 g.chr19:10599946A>G c.1630T>C c.(1630-1632)Tgg>Cgg p.W544R KIPAN 19 10602352 10602352 + Missense_Mutation SNP A A G TCGA-BP-5183-01A-01D-1429-08 TCGA-BP-5183-11A-01D-1429-08 g.chr19:10602352A>G c.1226T>C c.(1225-1227)aTg>aCg p.M409T KIPAN 19 10602767 10602767 + Missense_Mutation SNP C C A TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr19:10602767C>A c.811G>T c.(811-813)Gtg>Ttg p.V271L KIPAN 19 10610178 10610178 + Nonsense_Mutation SNP G G A TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr19:10610178G>A c.532C>T c.(532-534)Cag>Tag p.Q178* KIPAN 19 10610395 10610395 + Silent SNP A A G TCGA-BP-4973-01A-01D-1462-08 TCGA-BP-4973-11A-01D-1462-08 g.chr19:10610395A>G c.315T>C c.(313-315)ccT>ccC p.P105P KIPAN 19 10610566 10610566 + Silent SNP G G T TCGA-A4-A5XZ-01A-11D-A31X-10 TCGA-A4-A5XZ-10A-01D-A31X-10 g.chr19:10610566G>T c.144C>A c.(142-144)ggC>ggA p.G48G KIRC 19 10599946 10599946 + Missense_Mutation SNP A A G TCGA-B0-4815-01A-01D-1501-10 TCGA-B0-4815-11A-02D-1501-10 g.chr19:10599946A>G c.1630T>C c.(1630-1632)Tgg>Cgg p.W544R KIRC 19 10602352 10602352 + Missense_Mutation SNP A A G TCGA-BP-5183-01A-01D-1429-08 TCGA-BP-5183-11A-01D-1429-08 g.chr19:10602352A>G c.1226T>C c.(1225-1227)aTg>aCg p.M409T KIRC 19 10610395 10610395 + Silent SNP A A G TCGA-BP-4973-01A-01D-1462-08 TCGA-BP-4973-11A-01D-1462-08 g.chr19:10610395A>G c.315T>C c.(313-315)ccT>ccC p.P105P KIRP 19 10602767 10602767 + Missense_Mutation SNP C C A TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr19:10602767C>A c.811G>T c.(811-813)Gtg>Ttg p.V271L KIRP 19 10610178 10610178 + Nonsense_Mutation SNP G G A TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr19:10610178G>A c.532C>T c.(532-534)Cag>Tag p.Q178* KIRP 19 10610566 10610566 + Silent SNP G G T TCGA-A4-A5XZ-01A-11D-A31X-10 TCGA-A4-A5XZ-10A-01D-A31X-10 g.chr19:10610566G>T c.144C>A c.(142-144)ggC>ggA p.G48G LGG 19 10600040 10600040 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:10600040G>A c.1536C>T c.(1534-1536)gtC>gtT p.V512V LGG 19 10602360 10602360 + Silent SNP G G A TCGA-DU-A7TA-01A-11D-A33T-08 TCGA-DU-A7TA-10A-01D-A33W-08 g.chr19:10602360G>A c.1218C>T c.(1216-1218)tgC>tgT p.C406C LIHC 19 10597429 10597429 + Missense_Mutation SNP T T C TCGA-2Y-A9H3-01A-11D-A382-10 TCGA-2Y-A9H3-10A-01D-A385-10 g.chr19:10597429T>C c.1774A>G c.(1774-1776)Agc>Ggc p.S592G LIHC 19 10600002 10600002 + Missense_Mutation SNP T T C TCGA-ED-A4XI-01A-11D-A25V-10 TCGA-ED-A4XI-10A-01D-A25V-10 g.chr19:10600002T>C c.1574A>G c.(1573-1575)tAt>tGt p.Y525C LIHC 19 10600016 10600019 + Frame_Shift_Del DEL ATAG ATAG - TCGA-DD-AACO-01A-11D-A40R-10 TCGA-DD-AACO-10A-01D-A40U-10 g.chr19:10600016_10600019delATAG c.1557_1560delCTAT c.(1555-1560)atctatfs p.IY519fs LIHC 19 10602442 10602442 + Missense_Mutation SNP C C A TCGA-K7-A5RG-01A-11D-A28X-10 TCGA-K7-A5RG-10A-01D-A28X-10 g.chr19:10602442C>A c.1136G>T c.(1135-1137)gGc>gTc p.G379V LIHC 19 10602490 10602514 + Frame_Shift_Del DEL CTCCGCGGCACCTGCAGGTCCGCCA CTCCGCGGCACCTGCAGGTCCGCCA - TCGA-2Y-A9GS-01A-12D-A382-10 TCGA-2Y-A9GS-10A-01D-A385-10 g.chr19:10602490_10602514delCTCCGCGGCACCTGCAGGTCCGCCA c.1064_1088delTGGCGGACCTGCAGGTGCCGCGGAG c.(1063-1089)ttggcggacctgcaggtgccgcggagcfs p.LADLQVPRS355fs LIHC 19 10602646 10602646 + Missense_Mutation SNP T T A TCGA-DD-AADM-01A-11D-A40R-10 TCGA-DD-AADM-10A-01D-A40U-10 g.chr19:10602646T>A c.932A>T c.(931-933)cAc>cTc p.H311L LIHC 19 10602745 10602745 + Missense_Mutation SNP G G A TCGA-CC-A7IK-01A-12D-A33Q-10 TCGA-CC-A7IK-10A-01D-A33Q-10 g.chr19:10602745G>A c.833C>T c.(832-834)cCg>cTg p.P278L LIHC 19 10602767 10602767 + Missense_Mutation SNP C C A TCGA-DD-A1EL-01A-11D-A152-10 TCGA-DD-A1EL-10A-01D-A152-10 g.chr19:10602767C>A c.811G>T c.(811-813)Gtg>Ttg p.V271L LIHC 19 10602811 10602812 + Frame_Shift_Ins INS - - CGTA TCGA-G3-A3CK-01A-11D-A20W-10 TCGA-G3-A3CK-10A-01D-A20W-10 g.chr19:10602811_10602812insCGTA c.766_767insTACG c.(766-768)gacfs p.D256fs LIHC 19 10610154 10610154 + Missense_Mutation SNP C C T TCGA-BC-A8YO-01A-11D-A36X-10 TCGA-BC-A8YO-10A-01D-A370-10 g.chr19:10610154C>T c.556G>A c.(556-558)Ggc>Agc p.G186S LIHC 19 10610159 10610159 + Missense_Mutation SNP G G T TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr19:10610159G>T c.551C>A c.(550-552)gCc>gAc p.A184D LIHC 19 10610207 10610207 + Missense_Mutation SNP A A C TCGA-DD-AADM-01A-11D-A40R-10 TCGA-DD-AADM-10A-01D-A40U-10 g.chr19:10610207A>C c.503T>G c.(502-504)gTc>gGc p.V168G LIHC 19 10610240 10610240 + Missense_Mutation SNP T T C TCGA-DD-AAE7-01A-11D-A40R-10 TCGA-DD-AAE7-10A-01D-A40U-10 g.chr19:10610240T>C c.470A>G c.(469-471)aAc>aGc p.N157S LIHC 19 10610255 10610255 + Missense_Mutation SNP A A C TCGA-2Y-A9GY-01A-11D-A382-10 TCGA-2Y-A9GY-10A-01D-A385-10 g.chr19:10610255A>C c.455T>G c.(454-456)gTc>gGc p.V152G LIHC 19 10610300 10610300 + Missense_Mutation SNP A A G TCGA-DD-A4NR-01A-11D-A30V-10 TCGA-DD-A4NR-10A-01D-A30V-10 g.chr19:10610300A>G c.410T>C c.(409-411)aTt>aCt p.I137T LIHC 19 10610330 10610330 + Frame_Shift_Del DEL C C - TCGA-DD-AACB-01A-11D-A40R-10 TCGA-DD-AACB-10A-01D-A40U-10 g.chr19:10610330delC c.380delG c.(379-381)ggtfs p.G127fs LIHC 19 10610398 10610398 + Missense_Mutation SNP G G T TCGA-G3-A3CK-01A-11D-A20W-10 TCGA-G3-A3CK-10A-01D-A20W-10 g.chr19:10610398G>T c.312C>A c.(310-312)agC>agA p.S104R LIHC 19 10610421 10610421 + Nonsense_Mutation SNP T T A TCGA-DD-AACQ-01A-11D-A40R-10 TCGA-DD-AACQ-10A-01D-A40U-10 g.chr19:10610421T>A c.289A>T c.(289-291)Aag>Tag p.K97* LIHC 19 10610444 10610444 + Missense_Mutation SNP G G A TCGA-RC-A6M6-01A-11D-A32G-10 TCGA-RC-A6M6-10A-01D-A32G-10 g.chr19:10610444G>A c.266C>T c.(265-267)cCg>cTg p.P89L LUAD 19 10597355 10597355 + Missense_Mutation SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr19:10597355C>A c.1848G>T c.(1846-1848)caG>caT p.Q616H LUAD 19 10597367 10597367 + Frame_Shift_Del DEL G G - TCGA-44-A4SS-01A-11D-A24P-08 TCGA-44-A4SS-10A-01D-A24P-08 g.chr19:10597367delG c.1836delC c.(1834-1836)cccfs p.P612fs LUAD 19 10597393 10597393 + Frame_Shift_Del DEL C C - TCGA-MP-A4TE-01A-22D-A25L-08 TCGA-MP-A4TE-10A-01D-A25L-08 g.chr19:10597393delC c.1810delG c.(1810-1812)gtgfs p.V604fs LUAD 19 10597396 10597396 + Missense_Mutation SNP C C A TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chr19:10597396C>A c.1807G>T c.(1807-1809)Ggg>Tgg p.G603W LUAD 19 10597426 10597426 + Frame_Shift_Del DEL C C - TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr19:10597426delC c.1777delG c.(1777-1779)gagfs p.E593fs LUAD 19 10597491 10597491 + Missense_Mutation SNP C C T TCGA-NJ-A55R-01A-11D-A25L-08 TCGA-NJ-A55R-10A-01D-A25L-08 g.chr19:10597491C>T c.1712G>A c.(1711-1713)gGc>gAc p.G571D LUAD 19 10597495 10597495 + Splice_Site SNP C C A TCGA-44-7667-01A-31D-2063-08 TCGA-44-7667-10A-01D-2063-08 g.chr19:10597495C>A c.e6-1 LUAD 19 10599866 10599866 + Splice_Site SNP A A T TCGA-55-6972-01A-11D-1945-08 TCGA-55-6972-11A-01D-1945-08 g.chr19:10599866A>T c.e5+1 LUAD 19 10599867 10599867 + Splice_Site SNP C C A TCGA-55-A4DF-01A-11D-A24D-08 TCGA-55-A4DF-10A-01D-A24F-08 g.chr19:10599867C>A c.e5+1 LUAD 19 10599899 10599899 + Silent SNP G G A TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr19:10599899G>A c.1677C>T c.(1675-1677)atC>atT p.I559I LUAD 19 10599903 10599903 + Missense_Mutation SNP C C T TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr19:10599903C>T c.1673G>A c.(1672-1674)gGg>gAg p.G558E LUAD 19 10599915 10599915 + Missense_Mutation SNP C C T TCGA-99-8033-01A-11D-2238-08 TCGA-99-8033-10A-01D-2238-08 g.chr19:10599915C>T c.1661G>A c.(1660-1662)cGa>cAa p.R554Q LUAD 19 10599954 10599958 + Frame_Shift_Del DEL GTTTC GTTTC - TCGA-J2-8194-01A-11D-2238-08 TCGA-J2-8194-10A-01D-2238-08 g.chr19:10599954_10599958delGTTTC c.1618_1622delGAAAC c.(1618-1623)gaaacafs p.ET542fs LUAD 19 10599996 10599996 + Missense_Mutation SNP C C A TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr19:10599996C>A c.1580G>T c.(1579-1581)gGt>gTt p.G527V LUAD 19 10599997 10599997 + Missense_Mutation SNP C C A TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr19:10599997C>A c.1579G>T c.(1579-1581)Ggt>Tgt p.G527C LUAD 19 10600006 10600006 + Missense_Mutation SNP C C A TCGA-05-4384-01A-01D-1753-08 TCGA-05-4384-10A-01D-1753-08 g.chr19:10600006C>A c.1570G>T c.(1570-1572)Ggc>Tgc p.G524C LUAD 19 10600008 10600008 + Missense_Mutation SNP C C T TCGA-97-8176-01A-11D-2393-08 TCGA-97-8176-10B-01D-2393-08 g.chr19:10600008C>T c.1568G>A c.(1567-1569)gGg>gAg p.G523E LUAD 19 10600329 10600329 + Missense_Mutation SNP C C A TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr19:10600329C>A c.1526G>T c.(1525-1527)gGg>gTg p.G509V LUAD 19 10600330 10600330 + Missense_Mutation SNP C C A TCGA-55-5899-01A-11D-1625-08 TCGA-55-5899-10A-01D-1625-08 g.chr19:10600330C>A c.1525G>T c.(1525-1527)Ggg>Tgg p.G509W LUAD 19 10600347 10600347 + Missense_Mutation SNP A A T TCGA-49-4506-01A-01D-1265-08 TCGA-49-4506-11A-01D-1265-08 g.chr19:10600347A>T c.1508T>A c.(1507-1509)aTg>aAg p.M503K LUAD 19 10600356 10600356 + Frame_Shift_Del DEL A A - TCGA-17-Z036-01A-01W-0746-08 TCGA-17-Z036-11A-01W-0746-08 g.chr19:10600356delA c.1499delT c.(1498-1500)atcfs p.I500fs LUAD 19 10600365 10600365 + Missense_Mutation SNP C C A TCGA-78-7149-01A-11D-2036-08 TCGA-78-7149-10A-01D-2036-08 g.chr19:10600365C>A c.1490G>T c.(1489-1491)tGg>tTg p.W497L LUAD 19 10600380 10600380 + Frame_Shift_Del DEL G G - TCGA-78-7146-01A-11D-2036-08 TCGA-78-7146-10A-01D-2036-08 g.chr19:10600380delG c.1475delC c.(1474-1476)ccafs p.P492fs LUAD 19 10600417 10600417 + Missense_Mutation SNP C C A TCGA-78-7167-01A-11D-2063-08 TCGA-78-7167-11A-01D-2063-08 g.chr19:10600417C>A c.1438G>T c.(1438-1440)Ggg>Tgg p.G480W LUAD 19 10600417 10600417 + Missense_Mutation SNP C C A TCGA-MP-A4T7-01A-11D-A24P-08 TCGA-MP-A4T7-10A-01D-A24P-08 g.chr19:10600417C>A c.1438G>T c.(1438-1440)Ggg>Tgg p.G480W LUAD 19 10600419 10600419 + Missense_Mutation SNP T T C TCGA-05-4395-01A-01D-1265-08 TCGA-05-4395-10A-01D-1265-08 g.chr19:10600419T>C c.1436A>G c.(1435-1437)gAc>gGc p.D479G LUAD 19 10600425 10600425 + Frame_Shift_Del DEL C C - TCGA-78-7156-01A-11D-2036-08 TCGA-78-7156-10A-01D-2036-08 g.chr19:10600425delC c.1430delG c.(1429-1431)ggcfs p.G477fs LUAD 19 10600428 10600428 + Missense_Mutation SNP C C A TCGA-86-8674-01A-21D-2393-08 TCGA-86-8674-10A-01D-2393-08 g.chr19:10600428C>A c.1427G>T c.(1426-1428)gGg>gTg p.G476V LUAD 19 10600447 10600447 + Missense_Mutation SNP G G A TCGA-49-4507-01A-01D-1265-08 TCGA-49-4507-11A-01D-1265-08 g.chr19:10600447G>A c.1408C>T c.(1408-1410)Cgt>Tgt p.R470C LUAD 19 10600447 10600447 + Missense_Mutation SNP G G T TCGA-49-4514-01A-21D-1855-08 TCGA-49-4514-11A-01D-1855-08 g.chr19:10600447G>T c.1408C>A c.(1408-1410)Cgt>Agt p.R470S LUAD 19 10600473 10600479 + Frame_Shift_Del DEL ATCCTTC ATCCTTC - TCGA-62-A470-01A-11D-A24D-08 TCGA-62-A470-10A-01D-A24F-08 g.chr19:10600473_10600479delATCCTTC c.1376_1382delGAAGGAT c.(1375-1383)cgaaggatcfs p.RRI459fs LUAD 19 10600474 10600474 + Missense_Mutation SNP T T C TCGA-78-7158-01A-11D-2036-08 TCGA-78-7158-10A-01D-2036-08 g.chr19:10600474T>C c.1381A>G c.(1381-1383)Atc>Gtc p.I461V LUAD 19 10600477 10600477 + Missense_Mutation SNP T T C TCGA-05-4418-01A-01D-1265-08 TCGA-05-4418-10A-01D-1265-08 g.chr19:10600477T>C c.1378A>G c.(1378-1380)Agg>Ggg p.R460G LUAD 19 10602257 10602257 + Nonsense_Mutation SNP C C A TCGA-55-A492-01A-11D-A24D-08 TCGA-55-A492-10A-01D-A24F-08 g.chr19:10602257C>A c.1321G>T c.(1321-1323)Gag>Tag p.E441* LUAD 19 10602289 10602289 + Missense_Mutation SNP C C A TCGA-62-8398-01A-11D-2323-08 TCGA-62-8398-10A-01D-2323-08 g.chr19:10602289C>A c.1289G>T c.(1288-1290)gGc>gTc p.G430V LUAD 19 10602292 10602292 + Missense_Mutation SNP C C A TCGA-55-8085-01A-11D-2238-08 TCGA-55-8085-10A-01D-2238-08 g.chr19:10602292C>A c.1286G>T c.(1285-1287)gGc>gTc p.G429V LUAD 19 10602310 10602310 + Missense_Mutation SNP C C A TCGA-50-5068-01A-01D-1625-08 TCGA-50-5068-10A-01D-1625-08 g.chr19:10602310C>A c.1268G>T c.(1267-1269)gGc>gTc p.G423V LUAD 19 10602328 10602328 + Missense_Mutation SNP C C A TCGA-53-A4EZ-01A-12D-A24P-08 TCGA-53-A4EZ-10A-01D-A24P-08 g.chr19:10602328C>A c.1250G>T c.(1249-1251)gGg>gTg p.G417V LUAD 19 10602328 10602328 + Missense_Mutation SNP C C A TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr19:10602328C>A c.1250G>T c.(1249-1251)gGg>gTg p.G417V LUAD 19 10602328 10602328 + Missense_Mutation SNP C C T TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr19:10602328C>T c.1250G>A c.(1249-1251)gGg>gAg p.G417E LUAD 19 10602329 10602329 + Missense_Mutation SNP C C A TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr19:10602329C>A c.1249G>T c.(1249-1251)Ggg>Tgg p.G417W LUAD 19 10602329 10602329 + Missense_Mutation SNP C C T TCGA-50-5051-01A-21D-1855-08 TCGA-50-5051-10A-01D-1855-08 g.chr19:10602329C>T c.1249G>A c.(1249-1251)Ggg>Agg p.G417R LUAD 19 10602334 10602334 + Missense_Mutation SNP C C T TCGA-17-Z001-01A-01W-0746-08 TCGA-17-Z001-11A-01W-0746-08 g.chr19:10602334C>T c.1244G>A c.(1243-1245)cGc>cAc p.R415H LUAD 19 10602335 10602335 + Missense_Mutation SNP G G A TCGA-73-4676-01A-01D-1753-08 TCGA-73-4676-11A-01D-1753-08 g.chr19:10602335G>A c.1243C>T c.(1243-1245)Cgc>Tgc p.R415C LUAD 19 10602543 10602543 + Nonsense_Mutation SNP G G C TCGA-MP-A5C7-01A-11D-A25L-08 TCGA-MP-A5C7-10A-01D-A25L-08 g.chr19:10602543G>C c.1035C>G c.(1033-1035)taC>taG p.Y345* LUAD 19 10602581 10602581 + Missense_Mutation SNP C C A TCGA-78-7633-01A-11D-2063-08 TCGA-78-7633-10A-01D-2063-08 g.chr19:10602581C>A c.997G>T c.(997-999)Ggc>Tgc p.G333C LUAD 19 10602581 10602581 + Missense_Mutation SNP C C T TCGA-49-4486-01A-01D-1265-08 TCGA-49-4486-11A-01D-1265-08 g.chr19:10602581C>T c.997G>A c.(997-999)Ggc>Agc p.G333S LUAD 19 10602581 10602581 + Missense_Mutation SNP C C T TCGA-86-8281-01A-11D-2284-08 TCGA-86-8281-10A-01D-2284-08 g.chr19:10602581C>T c.997G>A c.(997-999)Ggc>Agc p.G333S LUAD 19 10602611 10602612 + Frame_Shift_Ins INS - - A TCGA-55-6970-01A-11D-1945-08 TCGA-55-6970-11A-01D-1945-08 g.chr19:10602611_10602612insA c.966_967insT c.(964-969)cccaagfs p.K323fs LUAD 19 10602620 10602620 + Missense_Mutation SNP G G A TCGA-75-7027-01A-11D-1945-08 TCGA-75-7027-10A-01D-1946-08 g.chr19:10602620G>A c.958C>T c.(958-960)Cgg>Tgg p.R320W LUAD 19 10602719 10602719 + Nonsense_Mutation SNP T T A TCGA-73-4677-01A-01D-1265-08 TCGA-73-4677-11A-01D-1265-08 g.chr19:10602719T>A c.859A>T c.(859-861)Aag>Tag p.K287* LUAD 19 10602727 10602727 + Missense_Mutation SNP T T A TCGA-49-4488-01A-01D-1753-08 TCGA-49-4488-11A-01D-1753-08 g.chr19:10602727T>A c.851A>T c.(850-852)cAg>cTg p.Q284L LUAD 19 10602727 10602727 + Missense_Mutation SNP T T A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr19:10602727T>A c.851A>T c.(850-852)cAg>cTg p.Q284L LUAD 19 10602739 10602739 + Missense_Mutation SNP A A T TCGA-78-7166-01A-12D-2063-08 TCGA-78-7166-11A-01D-2063-08 g.chr19:10602739A>T c.839T>A c.(838-840)tTc>tAc p.F280Y LUAD 19 10602746 10602746 + Missense_Mutation SNP G G A TCGA-44-7671-01A-11D-2063-08 TCGA-44-7671-10A-01D-2063-08 g.chr19:10602746G>A c.832C>T c.(832-834)Ccg>Tcg p.P278S LUAD 19 10602767 10602767 + Missense_Mutation SNP C C A TCGA-44-7669-01A-21D-2063-08 TCGA-44-7669-10A-01D-2063-08 g.chr19:10602767C>A c.811G>T c.(811-813)Gtg>Ttg p.V271L LUAD 19 10602767 10602767 + Missense_Mutation SNP C C T TCGA-44-7660-01A-11D-2063-08 TCGA-44-7660-10A-01D-2063-08 g.chr19:10602767C>T c.811G>A c.(811-813)Gtg>Atg p.V271M LUAD 19 10602775 10602775 + Missense_Mutation SNP A A G TCGA-49-6742-01A-11D-1855-08 TCGA-49-6742-11A-01D-1855-08 g.chr19:10602775A>G c.803T>C c.(802-804)cTg>cCg p.L268P LUAD 19 10602796 10602796 + Missense_Mutation SNP C C G TCGA-50-5939-01A-11D-1625-08 TCGA-50-5939-11A-01D-1625-08 g.chr19:10602796C>G c.782G>C c.(781-783)cGg>cCg p.R261P LUAD 19 10602799 10602799 + Missense_Mutation SNP C C A TCGA-17-Z043-01A-01W-0746-08 TCGA-17-Z043-11A-01W-0746-08 g.chr19:10602799C>A c.779G>T c.(778-780)cGa>cTa p.R260L LUAD 19 10602822 10602822 + Missense_Mutation SNP C C A TCGA-78-7154-01A-11D-2036-08 TCGA-78-7154-10A-01D-2036-08 g.chr19:10602822C>A c.756G>T c.(754-756)tgG>tgT p.W252C LUAD 19 10602840 10602840 + Missense_Mutation SNP G G C TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chr19:10602840G>C c.738C>G c.(736-738)ttC>ttG p.F246L LUAD 19 10602872 10602872 + Missense_Mutation SNP C C T TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr19:10602872C>T c.706G>A c.(706-708)Gac>Aac p.D236N LUAD 19 10602875 10602875 + Missense_Mutation SNP C C G TCGA-55-8510-01A-11D-2393-08 TCGA-55-8510-10A-01D-2393-08 g.chr19:10602875C>G c.703G>C c.(703-705)Gac>Cac p.D235H LUAD 19 10602923 10602923 + Missense_Mutation SNP C C G TCGA-97-A4M3-01A-11D-A24P-08 TCGA-97-A4M3-10A-01D-A24P-08 g.chr19:10602923C>G c.655G>C c.(655-657)Gag>Cag p.E219Q LUAD 19 10602925 10602925 + Missense_Mutation SNP T T A TCGA-73-7498-01A-12D-2184-08 TCGA-73-7498-10A-01D-2184-08 g.chr19:10602925T>A c.653A>T c.(652-654)gAg>gTg p.E218V LUAD 19 10602938 10602938 + Splice_Site SNP C C A TCGA-75-6206-01A-11D-1753-08 TCGA-75-6206-10A-01D-1753-08 g.chr19:10602938C>A c.640G>T c.(640-642)Gtg>Ttg p.V214L LUAD 19 10610099 10610099 + Missense_Mutation SNP C C G TCGA-75-6211-01A-11D-1753-08 TCGA-75-6211-10A-01D-1753-08 g.chr19:10610099C>G c.611G>C c.(610-612)cGg>cCg p.R204P LUAD 19 10610109 10610109 + Nonsense_Mutation SNP G G A TCGA-97-8179-01A-11D-2284-08 TCGA-97-8179-10A-01D-2284-08 g.chr19:10610109G>A c.601C>T c.(601-603)Cag>Tag p.Q201* LUAD 19 10610133 10610133 + Nonsense_Mutation SNP G G A TCGA-55-8505-01A-11D-2393-08 TCGA-55-8505-10A-01D-2393-08 g.chr19:10610133G>A c.577C>T c.(577-579)Cag>Tag p.Q193* LUAD 19 10610139 10610139 + Missense_Mutation SNP C C T TCGA-55-7815-01A-11D-2167-08 TCGA-55-7815-10A-01D-2167-08 g.chr19:10610139C>T c.571G>A c.(571-573)Gct>Act p.A191T LUAD 19 10610187 10610187 + Frame_Shift_Del DEL G G - TCGA-44-A47F-01A-11D-A24D-08 TCGA-44-A47F-10A-01D-A24F-08 g.chr19:10610187delG c.523delC c.(523-525)ctgfs p.L175fs LUAD 19 10610212 10610212 + Silent SNP G G A TCGA-MP-A4TI-01A-21D-A24P-08 TCGA-MP-A4TI-10A-01D-A24P-08 g.chr19:10610212G>A c.498C>T c.(496-498)agC>agT p.S166S LUAD 19 10610221 10610221 + Missense_Mutation SNP C C A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr19:10610221C>A c.489G>T c.(487-489)caG>caT p.Q163H LUAD 19 10610225 10610225 + Missense_Mutation SNP T T C TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chr19:10610225T>C c.485A>G c.(484-486)tAc>tGc p.Y162C LUAD 19 10610235 10610235 + Missense_Mutation SNP C C A TCGA-78-7162-01A-21D-2063-08 TCGA-78-7162-11A-01D-2063-08 g.chr19:10610235C>A c.475G>T c.(475-477)Gct>Tct p.A159S LUAD 19 10610235 10610235 + Missense_Mutation SNP C C G TCGA-91-6849-01A-11D-1945-08 TCGA-91-6849-11A-01D-1945-08 g.chr19:10610235C>G c.475G>C c.(475-477)Gct>Cct p.A159P LUAD 19 10610244 10610244 + Missense_Mutation SNP T T C TCGA-17-Z018-01A-01W-0746-08 TCGA-17-Z018-11A-01W-0746-08 g.chr19:10610244T>C c.466A>G c.(466-468)Atg>Gtg p.M156V LUAD 19 10610246 10610246 + Missense_Mutation SNP A A G TCGA-44-6776-01A-11D-1855-08 TCGA-44-6776-10A-01D-1855-08 g.chr19:10610246A>G c.464T>C c.(463-465)gTc>gCc p.V155A LUAD 19 10610277 10610277 + Missense_Mutation SNP T T A TCGA-17-Z030-01A-01W-0746-08 TCGA-17-Z030-11A-01W-0746-08 g.chr19:10610277T>A c.433A>T c.(433-435)Atc>Ttc p.I145F LUAD 19 10610279 10610279 + Missense_Mutation SNP G G A TCGA-17-Z011-01A-01W-0746-08 TCGA-17-Z011-11A-01W-0746-08 g.chr19:10610279G>A c.431C>T c.(430-432)tCc>tTc p.S144F LUAD 19 10610285 10610285 + Missense_Mutation SNP G G A TCGA-44-6779-01A-11D-1855-08 TCGA-44-6779-10A-01D-1855-08 g.chr19:10610285G>A c.425C>T c.(424-426)aCg>aTg p.T142M LUAD 19 10610293 10610293 + Missense_Mutation SNP G G T TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr19:10610293G>T c.417C>A c.(415-417)ttC>ttA p.F139L LUAD 19 10610343 10610343 + Missense_Mutation SNP C C A TCGA-73-4670-01A-01D-1265-08 TCGA-73-4670-11A-01D-1265-08 g.chr19:10610343C>A c.367G>T c.(367-369)Gtg>Ttg p.V123L LUAD 19 10610361 10610361 + Missense_Mutation SNP C C T TCGA-78-7153-01A-11D-2036-08 TCGA-78-7153-10A-01D-2036-08 g.chr19:10610361C>T c.349G>A c.(349-351)Gag>Aag p.E117K LUAD 19 10610364 10610364 + Missense_Mutation SNP G G A TCGA-55-6987-01A-11D-1945-08 TCGA-55-6987-11A-01D-1945-08 g.chr19:10610364G>A c.346C>T c.(346-348)Cgg>Tgg p.R116W LUAD 19 10610382 10610382 + Missense_Mutation SNP T T C TCGA-44-6778-01A-11D-1855-08 TCGA-44-6778-10A-01D-1855-08 g.chr19:10610382T>C c.328A>G c.(328-330)Atg>Gtg p.M110V LUAD 19 10610405 10610405 + Missense_Mutation SNP G G A TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr19:10610405G>A c.305C>T c.(304-306)tCa>tTa p.S102L LUAD 19 10610411 10610411 + Missense_Mutation SNP A A G TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr19:10610411A>G c.299T>C c.(298-300)cTg>cCg p.L100P LUAD 19 10610415 10610415 + Missense_Mutation SNP C C A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr19:10610415C>A c.295G>T c.(295-297)Gtg>Ttg p.V99L LUAD 19 10610419 10610419 + Missense_Mutation SNP C C A TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr19:10610419C>A c.291G>T c.(289-291)aaG>aaT p.K97N LUAD 19 10610475 10610475 + Missense_Mutation SNP C C G TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr19:10610475C>G c.235G>C c.(235-237)Gtc>Ctc p.V79L LUAD 19 10610574 10610574 + Nonsense_Mutation SNP G G A TCGA-50-5936-01A-11D-1625-08 TCGA-50-5936-11A-01D-1625-08 g.chr19:10610574G>A c.136C>T c.(136-138)Cag>Tag p.Q46* LUAD 19 10610589 10610589 + Nonsense_Mutation SNP C C A TCGA-69-8253-01A-11D-2284-08 TCGA-69-8253-10A-01D-2284-08 g.chr19:10610589C>A c.121G>T c.(121-123)Gag>Tag p.E41* LUSC 19 10599944 10599944 + Missense_Mutation SNP C C A TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr19:10599944C>A c.1632G>T c.(1630-1632)tgG>tgT p.W544C LUSC 19 10600339 10600339 + Missense_Mutation SNP T T C TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr19:10600339T>C c.1516A>G c.(1516-1518)Atc>Gtc p.I506V LUSC 19 10600376 10600376 + Missense_Mutation SNP C C G TCGA-18-5595-01A-01D-1632-08 TCGA-18-5595-11A-01D-1632-08 g.chr19:10600376C>G c.1479G>C c.(1477-1479)gaG>gaC p.E493D LUSC 19 10600417 10600417 + Missense_Mutation SNP C C A TCGA-37-5819-01A-01D-1632-08 TCGA-37-5819-10A-01D-1632-08 g.chr19:10600417C>A c.1438G>T c.(1438-1440)Ggg>Tgg p.G480W LUSC 19 10600417 10600417 + Missense_Mutation SNP C C A TCGA-60-2722-01A-01D-1522-08 TCGA-60-2722-11A-01D-1522-08 g.chr19:10600417C>A c.1438G>T c.(1438-1440)Ggg>Tgg p.G480W LUSC 19 10600447 10600447 + Missense_Mutation SNP G G A TCGA-60-2710-01A-01D-1522-08 TCGA-60-2710-11A-01D-1522-08 g.chr19:10600447G>A c.1408C>T c.(1408-1410)Cgt>Tgt p.R470C LUSC 19 10600447 10600447 + Missense_Mutation SNP G G A TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr19:10600447G>A c.1408C>T c.(1408-1410)Cgt>Tgt p.R470C LUSC 19 10600448 10600449 + Frame_Shift_Ins INS - - T TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr19:10600448_10600449insT c.1406_1407insA c.(1405-1407)aatfs p.N469fs LUSC 19 10602310 10602310 + Missense_Mutation SNP C C A TCGA-39-5036-01A-01D-1441-08 TCGA-39-5036-11A-01D-1441-08 g.chr19:10602310C>A c.1268G>T c.(1267-1269)gGc>gTc p.G423V LUSC 19 10602314 10602314 + Missense_Mutation SNP C C T TCGA-21-1077-01A-01D-1521-08 TCGA-21-1077-11A-01D-1521-08 g.chr19:10602314C>T c.1264G>A c.(1264-1266)Gat>Aat p.D422N LUSC 19 10602326 10602326 + Missense_Mutation SNP C C A TCGA-51-4081-01A-01D-1458-08 TCGA-51-4081-11A-01D-1458-08 g.chr19:10602326C>A c.1252G>T c.(1252-1254)Gtg>Ttg p.V418L LUSC 19 10602473 10602473 + Missense_Mutation SNP C C G TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr19:10602473C>G c.1105G>C c.(1105-1107)Gtg>Ctg p.V369L LUSC 19 10602619 10602619 + Missense_Mutation SNP C C T TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr19:10602619C>T c.959G>A c.(958-960)cGg>cAg p.R320Q LUSC 19 10602625 10602625 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr19:10602625G>A c.953C>T c.(952-954)cCc>cTc p.P318L LUSC 19 10602649 10602649 + Missense_Mutation SNP A A G TCGA-33-4538-01A-01D-1267-08 TCGA-33-4538-11A-01D-1267-08 g.chr19:10602649A>G c.929T>C c.(928-930)cTg>cCg p.L310P LUSC 19 10602799 10602799 + Missense_Mutation SNP C C T TCGA-18-5595-01A-01D-1632-08 TCGA-18-5595-11A-01D-1632-08 g.chr19:10602799C>T c.779G>A c.(778-780)cGa>cAa p.R260Q LUSC 19 10602850 10602850 + Missense_Mutation SNP G G C TCGA-37-4133-01A-01D-1352-08 TCGA-37-4133-10A-01D-1352-08 g.chr19:10602850G>C c.728C>G c.(727-729)tCc>tGc p.S243C LUSC 19 10602887 10602887 + Missense_Mutation SNP G G C TCGA-60-2723-01A-01D-1522-08 TCGA-60-2723-11A-01D-1522-08 g.chr19:10602887G>C c.691C>G c.(691-693)Ctc>Gtc p.L231V LUSC 19 10602907 10602907 + Missense_Mutation SNP G G T TCGA-66-2777-01A-01D-1267-08 TCGA-66-2777-11A-01D-1267-08 g.chr19:10602907G>T c.671C>A c.(670-672)tCc>tAc p.S224Y LUSC 19 10610211 10610211 + Missense_Mutation SNP C C A TCGA-43-2578-01A-01D-1522-08 TCGA-43-2578-11A-01D-1522-08 g.chr19:10610211C>A c.499G>T c.(499-501)Gtt>Ttt p.V167F LUSC 19 10610247 10610247 + Missense_Mutation SNP C C A TCGA-18-3407-01A-01D-0983-08 TCGA-18-3407-11A-01D-0983-08 g.chr19:10610247C>A c.463G>T c.(463-465)Gtc>Ttc p.V155F LUSC 19 10610247 10610247 + Missense_Mutation SNP C C A TCGA-22-4599-01A-01D-1441-08 TCGA-22-4599-11A-01D-1441-08 g.chr19:10610247C>A c.463G>T c.(463-465)Gtc>Ttc p.V155F LUSC 19 10610487 10610487 + Nonsense_Mutation SNP G G A TCGA-46-6025-01A-11D-1817-08 TCGA-46-6025-10A-01D-1817-08 g.chr19:10610487G>A c.223C>T c.(223-225)Cag>Tag p.Q75* LUSC 19 10610666 10610666 + Missense_Mutation SNP C C A TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr19:10610666C>A c.44G>T c.(43-45)cGa>cTa p.R15L OV 19 10610575 10610575 + Silent SNP G G T TCGA-24-2035-01A-01W-0722-08 TCGA-24-2035-10A-01W-0722-08 g.chr19:10610575G>T c.135C>A c.(133-135)tcC>tcA p.S45S PAAD 19 10599948 10599948 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:10599948G>A c.1628C>T c.(1627-1629)aCg>aTg p.T543M PAAD 19 10610147 10610147 + Missense_Mutation SNP G G C TCGA-S4-A8RO-01A-12D-A377-08 TCGA-S4-A8RO-10A-01D-A37A-08 g.chr19:10610147G>C c.563C>G c.(562-564)gCc>gGc p.A188G PRAD 19 10597450 10597450 + Missense_Mutation SNP C C T TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr19:10597450C>T c.1753G>A c.(1753-1755)Gac>Aac p.D585N PRAD 19 10602358 10602358 + Missense_Mutation SNP G G A TCGA-CH-5792-01A-11D-1576-08 TCGA-CH-5792-10A-01D-1576-08 g.chr19:10602358G>A c.1220C>T c.(1219-1221)gCc>gTc p.A407V PRAD 19 10602517 10602517 + Missense_Mutation SNP C C A TCGA-EJ-A46G-01A-31D-A26M-08 TCGA-EJ-A46G-10A-01D-A26K-08 g.chr19:10602517C>A c.1061G>T c.(1060-1062)cGg>cTg p.R354L PRAD 19 10610427 10610427 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:10610427C>T c.283G>A c.(283-285)Gcc>Acc p.A95T SARC 19 10610476 10610476 + Silent SNP G G A TCGA-3B-A9HT-01A-11D-A38Z-09 TCGA-3B-A9HT-10A-01D-A38Z-09 g.chr19:10610476G>A c.234C>T c.(232-234)gaC>gaT p.D78D SKCM 19 10600376 10600376 + Silent SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr19:10600376C>T c.1479G>A c.(1477-1479)gaG>gaA p.E493E SKCM 19 10600447 10600447 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr19:10600447G>A c.1408C>T c.(1408-1410)Cgt>Tgt p.R470C SKCM 19 10610321 10610321 + Missense_Mutation SNP G G A TCGA-D3-A2J7-06A-11D-A196-08 TCGA-D3-A2J7-10A-01D-A198-08 g.chr19:10610321G>A c.389C>T c.(388-390)cCc>cTc p.P130L SKCM 19 10610578 10610578 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr19:10610578G>A c.132C>T c.(130-132)ccC>ccT p.P44P

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 19 10599965 10599965 single base substitution G A 3_prime_UTR_variant BLCA-CN 19 10599965 10599965 single base substitution G A downstream_gene_variant BLCA-CN 19 10599965 10599965 single base substitution G A exon_variant BLCA-CN 19 10599965 10599965 single base substitution G A intron_variant BLCA-CN 19 10599965 10599965 single base substitution G A synonymous_variant Y537Y 1611C>T BLCA-US 19 10599968 10599968 insertion of <=200bp - CA 3_prime_UTR_variant BLCA-US 19 10599968 10599968 insertion of <=200bp - CA downstream_gene_variant BLCA-US 19 10599968 10599968 insertion of <=200bp - CA exon_variant BLCA-US 19 10599968 10599968 insertion of <=200bp - CA frameshift_variant R536R? BLCA-US 19 10599968 10599968 insertion of <=200bp - CA intron_variant BLCA-US 19 10602630 10602630 single base substitution C T downstream_gene_variant BLCA-US 19 10602630 10602630 single base substitution C T exon_variant BLCA-US 19 10602630 10602630 single base substitution C T synonymous_variant V316V 948G>A BLCA-US 19 10602630 10602630 single base substitution C T upstream_gene_variant BLCA-US 19 10602848 10602848 single base substitution C T 3_prime_UTR_variant BLCA-US 19 10602848 10602848 single base substitution C T downstream_gene_variant BLCA-US 19 10602848 10602848 single base substitution C T exon_variant BLCA-US 19 10602848 10602848 single base substitution C T missense_variant E244K 730G>A BLCA-US 19 10602848 10602848 single base substitution C T upstream_gene_variant BLCA-US 19 10602926 10602926 single base substitution C G 3_prime_UTR_variant BLCA-US 19 10602926 10602926 single base substitution C G downstream_gene_variant BLCA-US 19 10602926 10602926 single base substitution C G exon_variant BLCA-US 19 10602926 10602926 single base substitution C G missense_variant E218Q 652G>C BLCA-US 19 10602926 10602926 single base substitution C G upstream_gene_variant BLCA-US 19 10610363 10610363 single base substitution C G intron_variant BLCA-US 19 10610363 10610363 single base substitution C G missense_variant R116P 347G>C BLCA-US 19 10610363 10610363 single base substitution C G upstream_gene_variant BLCA-US 19 10610637 10610637 single base substitution C T intron_variant BLCA-US 19 10610637 10610637 single base substitution C T missense_variant E25K 73G>A BLCA-US 19 10610637 10610637 single base substitution C T upstream_gene_variant BRCA-EU 19 10591897 10591897 single base substitution G A downstream_gene_variant BRCA-EU 19 10592226 10592226 single base substitution G A downstream_gene_variant BRCA-EU 19 10592812 10592812 single base substitution G T downstream_gene_variant BRCA-EU 19 10592912 10592912 single base substitution C T downstream_gene_variant BRCA-EU 19 10593450 10593450 single base substitution G A downstream_gene_variant BRCA-EU 19 10593899 10593899 single base substitution T G downstream_gene_variant BRCA-EU 19 10595399 10595399 single base substitution A C downstream_gene_variant BRCA-EU 19 10595499 10595499 single base substitution G C downstream_gene_variant BRCA-EU 19 10596543 10596543 single base substitution C A downstream_gene_variant BRCA-EU 19 10596797 10596797 single base substitution A T 3_prime_UTR_variant BRCA-EU 19 10596797 10596797 single base substitution A T downstream_gene_variant BRCA-EU 19 10597096 10597096 single base substitution C A 3_prime_UTR_variant BRCA-EU 19 10597096 10597096 single base substitution C A downstream_gene_variant BRCA-EU 19 10598731 10598731 single base substitution C G downstream_gene_variant BRCA-EU 19 10598731 10598731 single base substitution C G intron_variant BRCA-EU 19 10599073 10599073 single base substitution G A downstream_gene_variant BRCA-EU 19 10599073 10599073 single base substitution G A intron_variant BRCA-EU 19 10599853 10599853 deletion of <=200bp C - downstream_gene_variant BRCA-EU 19 10599853 10599853 deletion of <=200bp C - intron_variant BRCA-EU 19 10600183 10600183 single base substitution G C downstream_gene_variant BRCA-EU 19 10600183 10600183 single base substitution G C intron_variant BRCA-EU 19 10600183 10600183 single base substitution G C upstream_gene_variant BRCA-EU 19 10600706 10600706 single base substitution T A downstream_gene_variant BRCA-EU 19 10600706 10600706 single base substitution T A intron_variant BRCA-EU 19 10600706 10600706 single base substitution T A upstream_gene_variant BRCA-EU 19 10603160 10603160 single base substitution C T intron_variant BRCA-EU 19 10603160 10603160 single base substitution C T upstream_gene_variant BRCA-EU 19 10605665 10605665 single base substitution C G downstream_gene_variant BRCA-EU 19 10605665 10605665 single base substitution C G intron_variant BRCA-EU 19 10605665 10605665 single base substitution C G upstream_gene_variant BRCA-EU 19 10606143 10606143 single base substitution G C downstream_gene_variant BRCA-EU 19 10606143 10606143 single base substitution G C intron_variant BRCA-EU 19 10606143 10606143 single base substitution G C upstream_gene_variant BRCA-EU 19 10606426 10606426 single base substitution G C downstream_gene_variant BRCA-EU 19 10606426 10606426 single base substitution G C intron_variant BRCA-EU 19 10606426 10606426 single base substitution G C upstream_gene_variant BRCA-EU 19 10607104 10607104 single base substitution G A downstream_gene_variant BRCA-EU 19 10607104 10607104 single base substitution G A intron_variant BRCA-EU 19 10607104 10607104 single base substitution G A upstream_gene_variant BRCA-EU 19 10608035 10608035 single base substitution G A downstream_gene_variant BRCA-EU 19 10608035 10608035 single base substitution G A intron_variant BRCA-EU 19 10608372 10608372 single base substitution G A downstream_gene_variant BRCA-EU 19 10608372 10608372 single base substitution G A intron_variant BRCA-EU 19 10610535 10610535 single base substitution G A intron_variant BRCA-EU 19 10610535 10610535 single base substitution G A missense_variant H59Y 175C>T BRCA-EU 19 10610535 10610535 single base substitution G A upstream_gene_variant BRCA-EU 19 10610552 10610552 single base substitution C A intron_variant BRCA-EU 19 10610552 10610552 single base substitution C A missense_variant S53I 158G>T BRCA-EU 19 10610552 10610552 single base substitution C A upstream_gene_variant BRCA-EU 19 10610719 10610719 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 19 10610719 10610719 single base substitution G A intron_variant BRCA-EU 19 10610719 10610719 single base substitution G A upstream_gene_variant BRCA-EU 19 10610881 10610881 single base substitution C G intron_variant BRCA-EU 19 10610881 10610881 single base substitution C G upstream_gene_variant BRCA-EU 19 10611023 10611023 single base substitution C T intron_variant BRCA-EU 19 10611023 10611023 single base substitution C T upstream_gene_variant BRCA-EU 19 10612442 10612442 single base substitution C T intron_variant BRCA-EU 19 10612442 10612442 single base substitution C T upstream_gene_variant BRCA-EU 19 10612911 10612911 single base substitution G C intron_variant BRCA-EU 19 10612911 10612911 single base substitution G C upstream_gene_variant BRCA-EU 19 10613883 10613883 single base substitution G T intron_variant BRCA-EU 19 10613883 10613883 single base substitution G T upstream_gene_variant BRCA-EU 19 10615212 10615212 single base substitution A G upstream_gene_variant BRCA-EU 19 10615537 10615537 single base substitution G T upstream_gene_variant BRCA-EU 19 10617675 10617675 single base substitution G C upstream_gene_variant BRCA-EU 19 10618510 10618510 single base substitution G A upstream_gene_variant BRCA-EU 19 10618969 10618969 single base substitution G A upstream_gene_variant BRCA-FR 19 10592912 10592912 single base substitution C T downstream_gene_variant BRCA-FR 19 10603417 10603417 single base substitution G C intron_variant BRCA-FR 19 10603417 10603417 single base substitution G C upstream_gene_variant BRCA-FR 19 10605665 10605665 single base substitution C G downstream_gene_variant BRCA-FR 19 10605665 10605665 single base substitution C G intron_variant BRCA-FR 19 10605665 10605665 single base substitution C G upstream_gene_variant BRCA-FR 19 10610719 10610719 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-FR 19 10610719 10610719 single base substitution G A intron_variant BRCA-FR 19 10610719 10610719 single base substitution G A upstream_gene_variant BRCA-FR 19 10611424 10611424 single base substitution T C intron_variant BRCA-FR 19 10611424 10611424 single base substitution T C upstream_gene_variant BRCA-FR 19 10611432 10611432 single base substitution T C intron_variant BRCA-FR 19 10611432 10611432 single base substitution T C upstream_gene_variant BRCA-FR 19 10615914 10615914 single base substitution G C upstream_gene_variant BRCA-US 19 10600498 10600498 insertion of <=200bp - T downstream_gene_variant BRCA-US 19 10600498 10600498 insertion of <=200bp - T frameshift_variant V453D? BRCA-US 19 10600498 10600498 insertion of <=200bp - T frameshift_variant V59D? BRCA-US 19 10600498 10600498 insertion of <=200bp - T intron_variant BRCA-US 19 10600498 10600498 insertion of <=200bp - T upstream_gene_variant BRCA-US 19 10600502 10600502 deletion of <=200bp G - downstream_gene_variant BRCA-US 19 10600502 10600502 deletion of <=200bp G - frameshift_variant H451 BRCA-US 19 10600502 10600502 deletion of <=200bp G - frameshift_variant H57 BRCA-US 19 10600502 10600502 deletion of <=200bp G - intron_variant BRCA-US 19 10600502 10600502 deletion of <=200bp G - upstream_gene_variant BRCA-US 19 10600510 10600510 single base substitution C A downstream_gene_variant BRCA-US 19 10600510 10600510 single base substitution C A intron_variant BRCA-US 19 10600510 10600510 single base substitution C A stop_gained E449* 1345G>T BRCA-US 19 10600510 10600510 single base substitution C A stop_gained E55* 163G>T BRCA-US 19 10600510 10600510 single base substitution C A upstream_gene_variant BRCA-US 19 10610217 10610217 single base substitution C T exon_variant BRCA-US 19 10610217 10610217 single base substitution C T missense_variant D165N 493G>A BRCA-US 19 10610217 10610217 single base substitution C T upstream_gene_variant BTCA-JP 19 10599965 10599965 single base substitution G A 3_prime_UTR_variant BTCA-JP 19 10599965 10599965 single base substitution G A downstream_gene_variant BTCA-JP 19 10599965 10599965 single base substitution G A exon_variant BTCA-JP 19 10599965 10599965 single base substitution G A intron_variant BTCA-JP 19 10599965 10599965 single base substitution G A synonymous_variant Y537Y 1611C>T BTCA-JP 19 10602602 10602602 single base substitution G A downstream_gene_variant BTCA-JP 19 10602602 10602602 single base substitution G A missense_variant R326C 976C>T BTCA-JP 19 10602602 10602602 single base substitution G A upstream_gene_variant BTCA-JP 19 10602636 10602636 single base substitution C T downstream_gene_variant BTCA-JP 19 10602636 10602636 single base substitution C T exon_variant BTCA-JP 19 10602636 10602636 single base substitution C T synonymous_variant T314T 942G>A BTCA-JP 19 10602636 10602636 single base substitution C T upstream_gene_variant CESC-US 19 10602878 10602878 single base substitution G A 3_prime_UTR_variant CESC-US 19 10602878 10602878 single base substitution G A downstream_gene_variant CESC-US 19 10602878 10602878 single base substitution G A exon_variant CESC-US 19 10602878 10602878 single base substitution G A missense_variant R234W 700C>T CESC-US 19 10602878 10602878 single base substitution G A upstream_gene_variant COAD-US 19 10600442 10600442 single base substitution G C downstream_gene_variant COAD-US 19 10600442 10600442 single base substitution G C intron_variant COAD-US 19 10600442 10600442 single base substitution G C synonymous_variant L471L 1413C>G COAD-US 19 10600442 10600442 single base substitution G C synonymous_variant L77L 231C>G COAD-US 19 10600442 10600442 single base substitution G C upstream_gene_variant COAD-US 19 10610217 10610217 single base substitution C T exon_variant COAD-US 19 10610217 10610217 single base substitution C T missense_variant D165N 493G>A COAD-US 19 10610217 10610217 single base substitution C T upstream_gene_variant COAD-US 19 10610686 10610686 single base substitution G A intron_variant COAD-US 19 10610686 10610686 single base substitution G A synonymous_variant S8S 24C>T COAD-US 19 10610686 10610686 single base substitution G A upstream_gene_variant COCA-CN 19 10600613 10600613 single base substitution T C downstream_gene_variant COCA-CN 19 10600613 10600613 single base substitution T C intron_variant COCA-CN 19 10600613 10600613 single base substitution T C upstream_gene_variant COCA-CN 19 10602942 10602942 single base substitution C T intron_variant COCA-CN 19 10602942 10602942 single base substitution C T splice_region_variant COCA-CN 19 10602942 10602942 single base substitution C T upstream_gene_variant COCA-CN 19 10610567 10610567 single base substitution C T intron_variant COCA-CN 19 10610567 10610567 single base substitution C T missense_variant G48D 143G>A COCA-CN 19 10610567 10610567 single base substitution C T upstream_gene_variant EOPC-DE 19 10594115 10594115 single base substitution A G downstream_gene_variant EOPC-DE 19 10612014 10612014 single base substitution A C intron_variant EOPC-DE 19 10612014 10612014 single base substitution A C upstream_gene_variant ESAD-UK 19 10591876 10591876 single base substitution C T downstream_gene_variant ESAD-UK 19 10593001 10593001 single base substitution G A downstream_gene_variant ESAD-UK 19 10593493 10593493 deletion of <=200bp A - downstream_gene_variant ESAD-UK 19 10593565 10593565 single base substitution C T downstream_gene_variant ESAD-UK 19 10594566 10594566 deletion of <=200bp T - downstream_gene_variant ESAD-UK 19 10595841 10595841 single base substitution G C downstream_gene_variant ESAD-UK 19 10595942 10595942 single base substitution A G downstream_gene_variant ESAD-UK 19 10602443 10602443 single base substitution C T downstream_gene_variant ESAD-UK 19 10602443 10602443 single base substitution C T exon_variant ESAD-UK 19 10602443 10602443 single base substitution C T missense_variant G379S 1135G>A ESAD-UK 19 10602443 10602443 single base substitution C T upstream_gene_variant ESAD-UK 19 10602773 10602773 single base substitution G A 3_prime_UTR_variant ESAD-UK 19 10602773 10602773 single base substitution G A downstream_gene_variant ESAD-UK 19 10602773 10602773 single base substitution G A exon_variant ESAD-UK 19 10602773 10602773 single base substitution G A missense_variant R269W 805C>T ESAD-UK 19 10602773 10602773 single base substitution G A upstream_gene_variant ESAD-UK 19 10603147 10603147 single base substitution C T intron_variant ESAD-UK 19 10603147 10603147 single base substitution C T upstream_gene_variant ESAD-UK 19 10604362 10604362 single base substitution C T intron_variant ESAD-UK 19 10604362 10604362 single base substitution C T upstream_gene_variant ESAD-UK 19 10604771 10604771 single base substitution C G intron_variant ESAD-UK 19 10604771 10604771 single base substitution C G upstream_gene_variant ESAD-UK 19 10606440 10606440 single base substitution G A downstream_gene_variant ESAD-UK 19 10606440 10606440 single base substitution G A intron_variant ESAD-UK 19 10606440 10606440 single base substitution G A upstream_gene_variant ESAD-UK 19 10608152 10608152 single base substitution T G downstream_gene_variant ESAD-UK 19 10608152 10608152 single base substitution T G intron_variant ESAD-UK 19 10610667 10610667 single base substitution G A intron_variant ESAD-UK 19 10610667 10610667 single base substitution G A stop_gained R15* 43C>T ESAD-UK 19 10610667 10610667 single base substitution G A upstream_gene_variant ESAD-UK 19 10610700 10610700 single base substitution C G intron_variant ESAD-UK 19 10610700 10610700 single base substitution C G missense_variant D4H 10G>C ESAD-UK 19 10610700 10610700 single base substitution C G upstream_gene_variant ESAD-UK 19 10610818 10610818 single base substitution C T intron_variant ESAD-UK 19 10610818 10610818 single base substitution C T upstream_gene_variant ESAD-UK 19 10610857 10610857 single base substitution C T intron_variant ESAD-UK 19 10610857 10610857 single base substitution C T upstream_gene_variant ESAD-UK 19 10610959 10610959 single base substitution C T intron_variant ESAD-UK 19 10610959 10610959 single base substitution C T upstream_gene_variant ESAD-UK 19 10610964 10610964 single base substitution C G intron_variant ESAD-UK 19 10610964 10610964 single base substitution C G upstream_gene_variant ESAD-UK 19 10611636 10611636 single base substitution G C intron_variant ESAD-UK 19 10611636 10611636 single base substitution G C upstream_gene_variant ESAD-UK 19 10611677 10611677 single base substitution C T intron_variant ESAD-UK 19 10611677 10611677 single base substitution C T upstream_gene_variant ESAD-UK 19 10612021 10612021 single base substitution C T intron_variant ESAD-UK 19 10612021 10612021 single base substitution C T upstream_gene_variant ESAD-UK 19 10612249 10612249 single base substitution T C intron_variant ESAD-UK 19 10612249 10612249 single base substitution T C upstream_gene_variant ESAD-UK 19 10613394 10613394 single base substitution C A 5_prime_UTR_variant ESAD-UK 19 10613394 10613394 single base substitution C A intron_variant ESAD-UK 19 10613394 10613394 single base substitution C A upstream_gene_variant ESCA-CN 19 10597488 10597488 single base substitution T C 3_prime_UTR_variant ESCA-CN 19 10597488 10597488 single base substitution T C exon_variant ESCA-CN 19 10597488 10597488 single base substitution T C missense_variant Y119C 356A>G ESCA-CN 19 10597488 10597488 single base substitution T C missense_variant Y572C 1715A>G ESCA-CN 19 10600401 10600401 single base substitution T C downstream_gene_variant ESCA-CN 19 10600401 10600401 single base substitution T C intron_variant ESCA-CN 19 10600401 10600401 single base substitution T C missense_variant N485S 1454A>G ESCA-CN 19 10600401 10600401 single base substitution T C missense_variant N91S 272A>G ESCA-CN 19 10600401 10600401 single base substitution T C upstream_gene_variant ESCA-CN 19 10600447 10600447 single base substitution G A downstream_gene_variant ESCA-CN 19 10600447 10600447 single base substitution G A intron_variant ESCA-CN 19 10600447 10600447 single base substitution G A missense_variant R470C 1408C>T ESCA-CN 19 10600447 10600447 single base substitution G A missense_variant R76C 226C>T ESCA-CN 19 10600447 10600447 single base substitution G A upstream_gene_variant ESCA-CN 19 10602314 10602314 single base substitution C T downstream_gene_variant ESCA-CN 19 10602314 10602314 single base substitution C T exon_variant ESCA-CN 19 10602314 10602314 single base substitution C T missense_variant D28N 82G>A ESCA-CN 19 10602314 10602314 single base substitution C T missense_variant D422N 1264G>A ESCA-CN 19 10602314 10602314 single base substitution C T upstream_gene_variant ESCA-CN 19 10602767 10602767 single base substitution C T 3_prime_UTR_variant ESCA-CN 19 10602767 10602767 single base substitution C T downstream_gene_variant ESCA-CN 19 10602767 10602767 single base substitution C T exon_variant ESCA-CN 19 10602767 10602767 single base substitution C T missense_variant V271M 811G>A ESCA-CN 19 10602767 10602767 single base substitution C T upstream_gene_variant ESCA-CN 19 10602869 10602869 single base substitution G T 3_prime_UTR_variant ESCA-CN 19 10602869 10602869 single base substitution G T downstream_gene_variant ESCA-CN 19 10602869 10602869 single base substitution G T exon_variant ESCA-CN 19 10602869 10602869 single base substitution G T missense_variant L237M 709C>A ESCA-CN 19 10602869 10602869 single base substitution G T upstream_gene_variant KIRC-US 19 10599946 10599946 single base substitution A G 3_prime_UTR_variant KIRC-US 19 10599946 10599946 single base substitution A G downstream_gene_variant KIRC-US 19 10599946 10599946 single base substitution A G exon_variant KIRC-US 19 10599946 10599946 single base substitution A G intron_variant KIRC-US 19 10599946 10599946 single base substitution A G missense_variant W544R 1630T>C KIRC-US 19 10602352 10602352 single base substitution A G downstream_gene_variant KIRC-US 19 10602352 10602352 single base substitution A G exon_variant KIRC-US 19 10602352 10602352 single base substitution A G missense_variant M15T 44T>C KIRC-US 19 10602352 10602352 single base substitution A G missense_variant M409T 1226T>C KIRC-US 19 10602352 10602352 single base substitution A G upstream_gene_variant KIRC-US 19 10610395 10610395 single base substitution A G intron_variant KIRC-US 19 10610395 10610395 single base substitution A G synonymous_variant P105P 315T>C KIRC-US 19 10610395 10610395 single base substitution A G upstream_gene_variant KIRP-US 19 10610178 10610178 single base substitution G A 3_prime_UTR_variant KIRP-US 19 10610178 10610178 single base substitution G A exon_variant KIRP-US 19 10610178 10610178 single base substitution G A stop_gained Q178* 532C>T KIRP-US 19 10610566 10610566 single base substitution G T intron_variant KIRP-US 19 10610566 10610566 single base substitution G T synonymous_variant G48G 144C>A KIRP-US 19 10610566 10610566 single base substitution G T upstream_gene_variant LAML-KR 19 10591845 10591845 single base substitution C T downstream_gene_variant LAML-KR 19 10599529 10599529 single base substitution C A downstream_gene_variant LAML-KR 19 10599529 10599529 single base substitution C A intron_variant LAML-KR 19 10599538 10599538 single base substitution T C downstream_gene_variant LAML-KR 19 10599538 10599538 single base substitution T C intron_variant LAML-KR 19 10599965 10599965 single base substitution G A 3_prime_UTR_variant LAML-KR 19 10599965 10599965 single base substitution G A downstream_gene_variant LAML-KR 19 10599965 10599965 single base substitution G A exon_variant LAML-KR 19 10599965 10599965 single base substitution G A intron_variant LAML-KR 19 10599965 10599965 single base substitution G A synonymous_variant Y537Y 1611C>T LAML-KR 19 10605308 10605308 single base substitution T C downstream_gene_variant LAML-KR 19 10605308 10605308 single base substitution T C intron_variant LAML-KR 19 10605308 10605308 single base substitution T C upstream_gene_variant LAML-KR 19 10607311 10607311 single base substitution C G downstream_gene_variant LAML-KR 19 10607311 10607311 single base substitution C G intron_variant LAML-KR 19 10607311 10607311 single base substitution C G upstream_gene_variant LAML-KR 19 10608939 10608939 single base substitution G A downstream_gene_variant LAML-KR 19 10608939 10608939 single base substitution G A intron_variant LAML-KR 19 10608945 10608945 single base substitution G A downstream_gene_variant LAML-KR 19 10608945 10608945 single base substitution G A intron_variant LICA-CN 19 10600395 10600395 single base substitution G T downstream_gene_variant LICA-CN 19 10600395 10600395 single base substitution G T intron_variant LICA-CN 19 10600395 10600395 single base substitution G T missense_variant A487D 1460C>A LICA-CN 19 10600395 10600395 single base substitution G T missense_variant A93D 278C>A LICA-CN 19 10600395 10600395 single base substitution G T upstream_gene_variant LICA-CN 19 10602698 10602698 single base substitution C A 3_prime_UTR_variant LICA-CN 19 10602698 10602698 single base substitution C A downstream_gene_variant LICA-CN 19 10602698 10602698 single base substitution C A exon_variant LICA-CN 19 10602698 10602698 single base substitution C A missense_variant D294Y 880G>T LICA-CN 19 10602698 10602698 single base substitution C A upstream_gene_variant LICA-CN 19 10602757 10602757 single base substitution T C 3_prime_UTR_variant LICA-CN 19 10602757 10602757 single base substitution T C downstream_gene_variant LICA-CN 19 10602757 10602757 single base substitution T C exon_variant LICA-CN 19 10602757 10602757 single base substitution T C missense_variant H274R 821A>G LICA-CN 19 10602757 10602757 single base substitution T C upstream_gene_variant LICA-CN 19 10602857 10602857 single base substitution A G 3_prime_UTR_variant LICA-CN 19 10602857 10602857 single base substitution A G downstream_gene_variant LICA-CN 19 10602857 10602857 single base substitution A G exon_variant LICA-CN 19 10602857 10602857 single base substitution A G missense_variant C241R 721T>C LICA-CN 19 10602857 10602857 single base substitution A G upstream_gene_variant LICA-FR 19 10597400 10597400 single base substitution C G 3_prime_UTR_variant LICA-FR 19 10597400 10597400 single base substitution C G exon_variant LICA-FR 19 10597400 10597400 single base substitution C G synonymous_variant R148R 444G>C LICA-FR 19 10597400 10597400 single base substitution C G synonymous_variant R601R 1803G>C LICA-FR 19 10597426 10597426 single base substitution C A 3_prime_UTR_variant LICA-FR 19 10597426 10597426 single base substitution C A exon_variant LICA-FR 19 10597426 10597426 single base substitution C A stop_gained E140* 418G>T LICA-FR 19 10597426 10597426 single base substitution C A stop_gained E593* 1777G>T LICA-FR 19 10599949 10599950 deletion of <=200bp TC - 3_prime_UTR_variant LICA-FR 19 10599949 10599950 deletion of <=200bp TC - downstream_gene_variant LICA-FR 19 10599949 10599950 deletion of <=200bp TC - exon_variant LICA-FR 19 10599949 10599950 deletion of <=200bp TC - frameshift_variant ET542 LICA-FR 19 10599949 10599950 deletion of <=200bp TC - intron_variant LICA-FR 19 10600531 10600531 single base substitution T A downstream_gene_variant LICA-FR 19 10600531 10600531 single base substitution T A intron_variant LICA-FR 19 10600531 10600531 single base substitution T A splice_acceptor_variant LICA-FR 19 10600531 10600531 single base substitution T A upstream_gene_variant LICA-FR 19 10602391 10602391 insertion of <=200bp - G downstream_gene_variant LICA-FR 19 10602391 10602391 insertion of <=200bp - G exon_variant LICA-FR 19 10602391 10602391 insertion of <=200bp - G frameshift_variant Y2Y? LICA-FR 19 10602391 10602391 insertion of <=200bp - G frameshift_variant Y396Y? LICA-FR 19 10602391 10602391 insertion of <=200bp - G upstream_gene_variant LICA-FR 19 10602442 10602442 single base substitution C T downstream_gene_variant LICA-FR 19 10602442 10602442 single base substitution C T exon_variant LICA-FR 19 10602442 10602442 single base substitution C T missense_variant G379D 1136G>A LICA-FR 19 10602442 10602442 single base substitution C T upstream_gene_variant LICA-FR 19 10602588 10602588 single base substitution G A downstream_gene_variant LICA-FR 19 10602588 10602588 single base substitution G A synonymous_variant T330T 990C>T LICA-FR 19 10602588 10602588 single base substitution G A upstream_gene_variant LICA-FR 19 10602589 10602590 deletion of <=200bp GT - downstream_gene_variant LICA-FR 19 10602589 10602590 deletion of <=200bp GT - frameshift_variant T330 LICA-FR 19 10602589 10602590 deletion of <=200bp GT - upstream_gene_variant LICA-FR 19 10602620 10602620 single base substitution G A downstream_gene_variant LICA-FR 19 10602620 10602620 single base substitution G A missense_variant R320W 958C>T LICA-FR 19 10602620 10602620 single base substitution G A upstream_gene_variant LICA-FR 19 10602767 10602767 single base substitution C A 3_prime_UTR_variant LICA-FR 19 10602767 10602767 single base substitution C A downstream_gene_variant LICA-FR 19 10602767 10602767 single base substitution C A exon_variant LICA-FR 19 10602767 10602767 single base substitution C A missense_variant V271L 811G>T LICA-FR 19 10602767 10602767 single base substitution C A upstream_gene_variant LICA-FR 19 10605254 10605254 single base substitution C A downstream_gene_variant LICA-FR 19 10605254 10605254 single base substitution C A intron_variant LICA-FR 19 10605254 10605254 single base substitution C A upstream_gene_variant LICA-FR 19 10608876 10608876 deletion of <=200bp T - downstream_gene_variant LICA-FR 19 10608876 10608876 deletion of <=200bp T - intron_variant LICA-FR 19 10610498 10610498 single base substitution C T intron_variant LICA-FR 19 10610498 10610498 single base substitution C T missense_variant R71Q 212G>A LICA-FR 19 10610498 10610498 single base substitution C T upstream_gene_variant LIHC-US 19 10600002 10600002 single base substitution T C downstream_gene_variant LIHC-US 19 10600002 10600002 single base substitution T C exon_variant LIHC-US 19 10600002 10600002 single base substitution T C intron_variant LIHC-US 19 10600002 10600002 single base substitution T C missense_variant Y525C 1574A>G LIHC-US 19 10602442 10602442 single base substitution C A downstream_gene_variant LIHC-US 19 10602442 10602442 single base substitution C A exon_variant LIHC-US 19 10602442 10602442 single base substitution C A missense_variant G379V 1136G>T LIHC-US 19 10602442 10602442 single base substitution C A upstream_gene_variant LIHC-US 19 10602745 10602745 single base substitution G A 3_prime_UTR_variant LIHC-US 19 10602745 10602745 single base substitution G A downstream_gene_variant LIHC-US 19 10602745 10602745 single base substitution G A exon_variant LIHC-US 19 10602745 10602745 single base substitution G A missense_variant P278L 833C>T LIHC-US 19 10602745 10602745 single base substitution G A upstream_gene_variant LIHC-US 19 10602767 10602767 single base substitution C A 3_prime_UTR_variant LIHC-US 19 10602767 10602767 single base substitution C A downstream_gene_variant LIHC-US 19 10602767 10602767 single base substitution C A exon_variant LIHC-US 19 10602767 10602767 single base substitution C A missense_variant V271L 811G>T LIHC-US 19 10602767 10602767 single base substitution C A upstream_gene_variant LIHC-US 19 10602811 10602811 insertion of <=200bp - CGTA 3_prime_UTR_variant LIHC-US 19 10602811 10602811 insertion of <=200bp - CGTA downstream_gene_variant LIHC-US 19 10602811 10602811 insertion of <=200bp - CGTA exon_variant LIHC-US 19 10602811 10602811 insertion of <=200bp - CGTA frameshift_variant D256DT? LIHC-US 19 10602811 10602811 insertion of <=200bp - CGTA upstream_gene_variant LIHC-US 19 10610300 10610300 single base substitution A G intron_variant LIHC-US 19 10610300 10610300 single base substitution A G missense_variant I137T 410T>C LIHC-US 19 10610300 10610300 single base substitution A G upstream_gene_variant LIHC-US 19 10610398 10610398 single base substitution G T intron_variant LIHC-US 19 10610398 10610398 single base substitution G T missense_variant S104R 312C>A LIHC-US 19 10610398 10610398 single base substitution G T upstream_gene_variant LINC-JP 19 10597226 10597226 single base substitution T C 3_prime_UTR_variant LINC-JP 19 10597226 10597226 single base substitution T C downstream_gene_variant LINC-JP 19 10597452 10597452 single base substitution T C 3_prime_UTR_variant LINC-JP 19 10597452 10597452 single base substitution T C exon_variant LINC-JP 19 10597452 10597452 single base substitution T C missense_variant Y131C 392A>G LINC-JP 19 10597452 10597452 single base substitution T C missense_variant Y584C 1751A>G LINC-JP 19 10597528 10597528 single base substitution G A intron_variant LINC-JP 19 10600625 10600625 single base substitution T C downstream_gene_variant LINC-JP 19 10600625 10600625 single base substitution T C intron_variant LINC-JP 19 10600625 10600625 single base substitution T C upstream_gene_variant LINC-JP 19 10602465 10602465 single base substitution G A downstream_gene_variant LINC-JP 19 10602465 10602465 single base substitution G A exon_variant LINC-JP 19 10602465 10602465 single base substitution G A synonymous_variant G371G 1113C>T LINC-JP 19 10602465 10602465 single base substitution G A upstream_gene_variant LINC-JP 19 10602831 10602831 deletion of <=200bp G - 3_prime_UTR_variant LINC-JP 19 10602831 10602831 deletion of <=200bp G - downstream_gene_variant LINC-JP 19 10602831 10602831 deletion of <=200bp G - exon_variant LINC-JP 19 10602831 10602831 deletion of <=200bp G - frameshift_variant C249 LINC-JP 19 10602831 10602831 deletion of <=200bp G - upstream_gene_variant LINC-JP 19 10602836 10602836 single base substitution C T 3_prime_UTR_variant LINC-JP 19 10602836 10602836 single base substitution C T downstream_gene_variant LINC-JP 19 10602836 10602836 single base substitution C T exon_variant LINC-JP 19 10602836 10602836 single base substitution C T missense_variant A248T 742G>A LINC-JP 19 10602836 10602836 single base substitution C T upstream_gene_variant LINC-JP 19 10602856 10602856 single base substitution C T 3_prime_UTR_variant LINC-JP 19 10602856 10602856 single base substitution C T downstream_gene_variant LINC-JP 19 10602856 10602856 single base substitution C T exon_variant LINC-JP 19 10602856 10602856 single base substitution C T missense_variant C241Y 722G>A LINC-JP 19 10602856 10602856 single base substitution C T upstream_gene_variant LINC-JP 19 10610523 10610523 single base substitution C T intron_variant LINC-JP 19 10610523 10610523 single base substitution C T missense_variant A63T 187G>A LINC-JP 19 10610523 10610523 single base substitution C T upstream_gene_variant LINC-JP 19 10610570 10610570 single base substitution T C intron_variant LINC-JP 19 10610570 10610570 single base substitution T C missense_variant H47R 140A>G LINC-JP 19 10610570 10610570 single base substitution T C upstream_gene_variant LIRI-JP 19 10593870 10593870 single base substitution C A downstream_gene_variant LIRI-JP 19 10593989 10593989 single base substitution T C downstream_gene_variant LIRI-JP 19 10594651 10594651 single base substitution A G downstream_gene_variant LIRI-JP 19 10597552 10597552 single base substitution G T intron_variant LIRI-JP 19 10597913 10597913 single base substitution T C downstream_gene_variant LIRI-JP 19 10597913 10597913 single base substitution T C intron_variant LIRI-JP 19 10599915 10599915 single base substitution C T 3_prime_UTR_variant LIRI-JP 19 10599915 10599915 single base substitution C T downstream_gene_variant LIRI-JP 19 10599915 10599915 single base substitution C T exon_variant LIRI-JP 19 10599915 10599915 single base substitution C T intron_variant LIRI-JP 19 10599915 10599915 single base substitution C T missense_variant R554Q 1661G>A LIRI-JP 19 10600446 10600446 single base substitution C T downstream_gene_variant LIRI-JP 19 10600446 10600446 single base substitution C T intron_variant LIRI-JP 19 10600446 10600446 single base substitution C T missense_variant R470H 1409G>A LIRI-JP 19 10600446 10600446 single base substitution C T missense_variant R76H 227G>A LIRI-JP 19 10600446 10600446 single base substitution C T upstream_gene_variant LIRI-JP 19 10600476 10600476 single base substitution C A downstream_gene_variant LIRI-JP 19 10600476 10600476 single base substitution C A intron_variant LIRI-JP 19 10600476 10600476 single base substitution C A missense_variant R460M 1379G>T LIRI-JP 19 10600476 10600476 single base substitution C A missense_variant R66M 197G>T LIRI-JP 19 10600476 10600476 single base substitution C A upstream_gene_variant LIRI-JP 19 10602475 10602475 single base substitution C T downstream_gene_variant LIRI-JP 19 10602475 10602475 single base substitution C T exon_variant LIRI-JP 19 10602475 10602475 single base substitution C T missense_variant C368Y 1103G>A LIRI-JP 19 10602475 10602475 single base substitution C T upstream_gene_variant LIRI-JP 19 10602780 10602780 single base substitution C T 3_prime_UTR_variant LIRI-JP 19 10602780 10602780 single base substitution C T downstream_gene_variant LIRI-JP 19 10602780 10602780 single base substitution C T exon_variant LIRI-JP 19 10602780 10602780 single base substitution C T synonymous_variant A266A 798G>A LIRI-JP 19 10602780 10602780 single base substitution C T upstream_gene_variant LIRI-JP 19 10604124 10604124 single base substitution C T intron_variant LIRI-JP 19 10604124 10604124 single base substitution C T upstream_gene_variant LIRI-JP 19 10604599 10604599 single base substitution A C intron_variant LIRI-JP 19 10604599 10604599 single base substitution A C upstream_gene_variant LIRI-JP 19 10607792 10607792 single base substitution T C downstream_gene_variant LIRI-JP 19 10607792 10607792 single base substitution T C intron_variant LIRI-JP 19 10610227 10610227 single base substitution C T exon_variant LIRI-JP 19 10610227 10610227 single base substitution C T missense_variant M161I 483G>A LIRI-JP 19 10610227 10610227 single base substitution C T upstream_gene_variant LIRI-JP 19 10612712 10612712 single base substitution C T intron_variant LIRI-JP 19 10612712 10612712 single base substitution C T upstream_gene_variant LUSC-KR 19 10595013 10595013 single base substitution G A downstream_gene_variant LUSC-KR 19 10595887 10595887 single base substitution G A downstream_gene_variant LUSC-KR 19 10596231 10596231 single base substitution G A downstream_gene_variant LUSC-KR 19 10598575 10598575 single base substitution C A downstream_gene_variant LUSC-KR 19 10598575 10598575 single base substitution C A intron_variant LUSC-KR 19 10598919 10598919 single base substitution C T downstream_gene_variant LUSC-KR 19 10598919 10598919 single base substitution C T intron_variant LUSC-KR 19 10600408 10600408 single base substitution G T downstream_gene_variant LUSC-KR 19 10600408 10600408 single base substitution G T intron_variant LUSC-KR 19 10600408 10600408 single base substitution G T missense_variant R483S 1447C>A LUSC-KR 19 10600408 10600408 single base substitution G T missense_variant R89S 265C>A LUSC-KR 19 10600408 10600408 single base substitution G T upstream_gene_variant LUSC-KR 19 10600446 10600446 single base substitution C T downstream_gene_variant LUSC-KR 19 10600446 10600446 single base substitution C T intron_variant LUSC-KR 19 10600446 10600446 single base substitution C T missense_variant R470H 1409G>A LUSC-KR 19 10600446 10600446 single base substitution C T missense_variant R76H 227G>A LUSC-KR 19 10600446 10600446 single base substitution C T upstream_gene_variant LUSC-KR 19 10602446 10602446 single base substitution C A downstream_gene_variant LUSC-KR 19 10602446 10602446 single base substitution C A exon_variant LUSC-KR 19 10602446 10602446 single base substitution C A missense_variant G378C 1132G>T LUSC-KR 19 10602446 10602446 single base substitution C A upstream_gene_variant LUSC-KR 19 10606207 10606207 single base substitution C A downstream_gene_variant LUSC-KR 19 10606207 10606207 single base substitution C A intron_variant LUSC-KR 19 10606207 10606207 single base substitution C A upstream_gene_variant LUSC-KR 19 10609300 10609300 single base substitution G C downstream_gene_variant LUSC-KR 19 10609300 10609300 single base substitution G C intron_variant LUSC-KR 19 10609636 10609636 single base substitution G A downstream_gene_variant LUSC-KR 19 10609636 10609636 single base substitution G A intron_variant LUSC-KR 19 10614381 10614381 single base substitution G A 5_prime_UTR_variant LUSC-KR 19 10614381 10614381 single base substitution G A upstream_gene_variant LUSC-KR 19 10618645 10618645 single base substitution G T upstream_gene_variant LUSC-US 19 10599944 10599944 single base substitution C A 3_prime_UTR_variant LUSC-US 19 10599944 10599944 single base substitution C A downstream_gene_variant LUSC-US 19 10599944 10599944 single base substitution C A exon_variant LUSC-US 19 10599944 10599944 single base substitution C A intron_variant LUSC-US 19 10599944 10599944 single base substitution C A missense_variant W544C 1632G>T LUSC-US 19 10600339 10600339 single base substitution T C downstream_gene_variant LUSC-US 19 10600339 10600339 single base substitution T C intron_variant LUSC-US 19 10600339 10600339 single base substitution T C missense_variant I112V 334A>G LUSC-US 19 10600339 10600339 single base substitution T C missense_variant I506V 1516A>G LUSC-US 19 10600339 10600339 single base substitution T C upstream_gene_variant LUSC-US 19 10600376 10600376 single base substitution C G downstream_gene_variant LUSC-US 19 10600376 10600376 single base substitution C G intron_variant LUSC-US 19 10600376 10600376 single base substitution C G missense_variant E493D 1479G>C LUSC-US 19 10600376 10600376 single base substitution C G missense_variant E99D 297G>C LUSC-US 19 10600376 10600376 single base substitution C G upstream_gene_variant LUSC-US 19 10600417 10600417 single base substitution C A downstream_gene_variant LUSC-US 19 10600417 10600417 single base substitution C A intron_variant LUSC-US 19 10600417 10600417 single base substitution C A missense_variant G480W 1438G>T LUSC-US 19 10600417 10600417 single base substitution C A missense_variant G86W 256G>T LUSC-US 19 10600417 10600417 single base substitution C A upstream_gene_variant LUSC-US 19 10600447 10600447 single base substitution G A downstream_gene_variant LUSC-US 19 10600447 10600447 single base substitution G A intron_variant LUSC-US 19 10600447 10600447 single base substitution G A missense_variant R470C 1408C>T LUSC-US 19 10600447 10600447 single base substitution G A missense_variant R76C 226C>T LUSC-US 19 10600447 10600447 single base substitution G A upstream_gene_variant LUSC-US 19 10600448 10600448 insertion of <=200bp - T downstream_gene_variant LUSC-US 19 10600448 10600448 insertion of <=200bp - T frameshift_variant N469N? LUSC-US 19 10600448 10600448 insertion of <=200bp - T frameshift_variant N75N? LUSC-US 19 10600448 10600448 insertion of <=200bp - T intron_variant LUSC-US 19 10600448 10600448 insertion of <=200bp - T upstream_gene_variant LUSC-US 19 10602310 10602310 single base substitution C A downstream_gene_variant LUSC-US 19 10602310 10602310 single base substitution C A exon_variant LUSC-US 19 10602310 10602310 single base substitution C A missense_variant G29V 86G>T LUSC-US 19 10602310 10602310 single base substitution C A missense_variant G423V 1268G>T LUSC-US 19 10602310 10602310 single base substitution C A upstream_gene_variant LUSC-US 19 10602314 10602314 single base substitution C T downstream_gene_variant LUSC-US 19 10602314 10602314 single base substitution C T exon_variant LUSC-US 19 10602314 10602314 single base substitution C T missense_variant D28N 82G>A LUSC-US 19 10602314 10602314 single base substitution C T missense_variant D422N 1264G>A LUSC-US 19 10602314 10602314 single base substitution C T upstream_gene_variant LUSC-US 19 10602326 10602326 single base substitution C A downstream_gene_variant LUSC-US 19 10602326 10602326 single base substitution C A exon_variant LUSC-US 19 10602326 10602326 single base substitution C A missense_variant V24L 70G>T LUSC-US 19 10602326 10602326 single base substitution C A missense_variant V418L 1252G>T LUSC-US 19 10602326 10602326 single base substitution C A upstream_gene_variant LUSC-US 19 10602473 10602473 single base substitution C G downstream_gene_variant LUSC-US 19 10602473 10602473 single base substitution C G exon_variant LUSC-US 19 10602473 10602473 single base substitution C G missense_variant V369L 1105G>C LUSC-US 19 10602473 10602473 single base substitution C G upstream_gene_variant LUSC-US 19 10602619 10602619 single base substitution C T downstream_gene_variant LUSC-US 19 10602619 10602619 single base substitution C T missense_variant R320Q 959G>A LUSC-US 19 10602619 10602619 single base substitution C T upstream_gene_variant LUSC-US 19 10602625 10602625 single base substitution G A downstream_gene_variant LUSC-US 19 10602625 10602625 single base substitution G A exon_variant LUSC-US 19 10602625 10602625 single base substitution G A missense_variant P318L 953C>T LUSC-US 19 10602625 10602625 single base substitution G A upstream_gene_variant LUSC-US 19 10602649 10602649 single base substitution A G downstream_gene_variant LUSC-US 19 10602649 10602649 single base substitution A G exon_variant LUSC-US 19 10602649 10602649 single base substitution A G missense_variant L310P 929T>C LUSC-US 19 10602649 10602649 single base substitution A G upstream_gene_variant LUSC-US 19 10602799 10602799 single base substitution C T 3_prime_UTR_variant LUSC-US 19 10602799 10602799 single base substitution C T downstream_gene_variant LUSC-US 19 10602799 10602799 single base substitution C T exon_variant LUSC-US 19 10602799 10602799 single base substitution C T missense_variant R260Q 779G>A LUSC-US 19 10602799 10602799 single base substitution C T upstream_gene_variant LUSC-US 19 10602850 10602850 single base substitution G C 3_prime_UTR_variant LUSC-US 19 10602850 10602850 single base substitution G C downstream_gene_variant LUSC-US 19 10602850 10602850 single base substitution G C exon_variant LUSC-US 19 10602850 10602850 single base substitution G C missense_variant S243C 728C>G LUSC-US 19 10602850 10602850 single base substitution G C upstream_gene_variant LUSC-US 19 10602887 10602887 single base substitution G C 3_prime_UTR_variant LUSC-US 19 10602887 10602887 single base substitution G C downstream_gene_variant LUSC-US 19 10602887 10602887 single base substitution G C exon_variant LUSC-US 19 10602887 10602887 single base substitution G C missense_variant L231V 691C>G LUSC-US 19 10602887 10602887 single base substitution G C upstream_gene_variant LUSC-US 19 10602907 10602907 single base substitution G T 3_prime_UTR_variant LUSC-US 19 10602907 10602907 single base substitution G T downstream_gene_variant LUSC-US 19 10602907 10602907 single base substitution G T exon_variant LUSC-US 19 10602907 10602907 single base substitution G T missense_variant S224Y 671C>A LUSC-US 19 10602907 10602907 single base substitution G T upstream_gene_variant LUSC-US 19 10610211 10610211 single base substitution C A exon_variant LUSC-US 19 10610211 10610211 single base substitution C A missense_variant V167F 499G>T LUSC-US 19 10610211 10610211 single base substitution C A upstream_gene_variant LUSC-US 19 10610247 10610247 single base substitution C A exon_variant LUSC-US 19 10610247 10610247 single base substitution C A missense_variant V155F 463G>T LUSC-US 19 10610247 10610247 single base substitution C A upstream_gene_variant LUSC-US 19 10610487 10610487 single base substitution G A intron_variant LUSC-US 19 10610487 10610487 single base substitution G A stop_gained Q75* 223C>T LUSC-US 19 10610487 10610487 single base substitution G A upstream_gene_variant LUSC-US 19 10610666 10610666 single base substitution C A intron_variant LUSC-US 19 10610666 10610666 single base substitution C A missense_variant R15L 44G>T LUSC-US 19 10610666 10610666 single base substitution C A upstream_gene_variant MALY-DE 19 10593493 10593493 insertion of <=200bp - A downstream_gene_variant MALY-DE 19 10607639 10607639 single base substitution A C downstream_gene_variant MALY-DE 19 10607639 10607639 single base substitution A C intron_variant MALY-DE 19 10613515 10613515 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant MALY-DE 19 10613515 10613515 single base substitution C A intron_variant MALY-DE 19 10613515 10613515 single base substitution C A upstream_gene_variant MELA-AU 19 10591941 10591941 single base substitution G A downstream_gene_variant MELA-AU 19 10592072 10592072 single base substitution C T downstream_gene_variant MELA-AU 19 10592672 10592672 single base substitution C T downstream_gene_variant MELA-AU 19 10593004 10593004 single base substitution G A downstream_gene_variant MELA-AU 19 10593469 10593469 single base substitution G A downstream_gene_variant MELA-AU 19 10594089 10594089 single base substitution C T downstream_gene_variant MELA-AU 19 10594104 10594104 single base substitution C T downstream_gene_variant MELA-AU 19 10594251 10594251 single base substitution G A downstream_gene_variant MELA-AU 19 10594475 10594475 single base substitution C T downstream_gene_variant MELA-AU 19 10594590 10594590 single base substitution T C downstream_gene_variant MELA-AU 19 10595185 10595185 single base substitution T A downstream_gene_variant MELA-AU 19 10595299 10595299 single base substitution C T downstream_gene_variant MELA-AU 19 10595899 10595899 single base substitution C T downstream_gene_variant MELA-AU 19 10595940 10595940 single base substitution G A downstream_gene_variant MELA-AU 19 10596303 10596303 single base substitution C T downstream_gene_variant MELA-AU 19 10596474 10596474 single base substitution G A downstream_gene_variant MELA-AU 19 10596849 10596849 single base substitution G A 3_prime_UTR_variant MELA-AU 19 10596849 10596849 single base substitution G A downstream_gene_variant MELA-AU 19 10598438 10598438 single base substitution G A downstream_gene_variant MELA-AU 19 10598438 10598438 single base substitution G A intron_variant MELA-AU 19 10598938 10598938 single base substitution G A downstream_gene_variant MELA-AU 19 10598938 10598938 single base substitution G A intron_variant MELA-AU 19 10599533 10599533 single base substitution G A downstream_gene_variant MELA-AU 19 10599533 10599533 single base substitution G A intron_variant MELA-AU 19 10599534 10599534 single base substitution G A downstream_gene_variant MELA-AU 19 10599534 10599534 single base substitution G A intron_variant MELA-AU 19 10599745 10599745 single base substitution G A downstream_gene_variant MELA-AU 19 10599745 10599745 single base substitution G A intron_variant MELA-AU 19 10599830 10599831 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 10599830 10599831 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 10600582 10600582 single base substitution G A downstream_gene_variant MELA-AU 19 10600582 10600582 single base substitution G A intron_variant MELA-AU 19 10600582 10600582 single base substitution G A upstream_gene_variant MELA-AU 19 10600636 10600636 single base substitution G A downstream_gene_variant MELA-AU 19 10600636 10600636 single base substitution G A intron_variant MELA-AU 19 10600636 10600636 single base substitution G A upstream_gene_variant MELA-AU 19 10600651 10600651 single base substitution G A downstream_gene_variant MELA-AU 19 10600651 10600651 single base substitution G A intron_variant MELA-AU 19 10600651 10600651 single base substitution G A upstream_gene_variant MELA-AU 19 10601526 10601526 single base substitution C T downstream_gene_variant MELA-AU 19 10601526 10601526 single base substitution C T intron_variant MELA-AU 19 10601526 10601526 single base substitution C T upstream_gene_variant MELA-AU 19 10601676 10601676 single base substitution C T downstream_gene_variant MELA-AU 19 10601676 10601676 single base substitution C T intron_variant MELA-AU 19 10601676 10601676 single base substitution C T upstream_gene_variant MELA-AU 19 10602291 10602291 single base substitution G A downstream_gene_variant MELA-AU 19 10602291 10602291 single base substitution G A exon_variant MELA-AU 19 10602291 10602291 single base substitution G A synonymous_variant G35G 105C>T MELA-AU 19 10602291 10602291 single base substitution G A synonymous_variant G429G 1287C>T MELA-AU 19 10602291 10602291 single base substitution G A upstream_gene_variant MELA-AU 19 10602572 10602572 single base substitution G A downstream_gene_variant MELA-AU 19 10602572 10602572 single base substitution G A stop_gained R336* 1006C>T MELA-AU 19 10602572 10602572 single base substitution G A upstream_gene_variant MELA-AU 19 10602573 10602573 single base substitution G A downstream_gene_variant MELA-AU 19 10602573 10602573 single base substitution G A synonymous_variant F335F 1005C>T MELA-AU 19 10602573 10602573 single base substitution G A upstream_gene_variant MELA-AU 19 10602918 10602918 single base substitution G A 3_prime_UTR_variant MELA-AU 19 10602918 10602918 single base substitution G A downstream_gene_variant MELA-AU 19 10602918 10602918 single base substitution G A exon_variant MELA-AU 19 10602918 10602918 single base substitution G A synonymous_variant F220F 660C>T MELA-AU 19 10602918 10602918 single base substitution G A upstream_gene_variant MELA-AU 19 10603695 10603696 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 10603695 10603696 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 10605441 10605442 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 10605441 10605442 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 10605441 10605442 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 10605746 10605746 single base substitution C T downstream_gene_variant MELA-AU 19 10605746 10605746 single base substitution C T intron_variant MELA-AU 19 10605746 10605746 single base substitution C T upstream_gene_variant MELA-AU 19 10606484 10606484 single base substitution G A downstream_gene_variant MELA-AU 19 10606484 10606484 single base substitution G A intron_variant MELA-AU 19 10606484 10606484 single base substitution G A upstream_gene_variant MELA-AU 19 10606852 10606852 single base substitution G A downstream_gene_variant MELA-AU 19 10606852 10606852 single base substitution G A intron_variant MELA-AU 19 10606852 10606852 single base substitution G A upstream_gene_variant MELA-AU 19 10607069 10607069 single base substitution G T downstream_gene_variant MELA-AU 19 10607069 10607069 single base substitution G T intron_variant MELA-AU 19 10607069 10607069 single base substitution G T upstream_gene_variant MELA-AU 19 10607375 10607375 single base substitution G T downstream_gene_variant MELA-AU 19 10607375 10607375 single base substitution G T intron_variant MELA-AU 19 10607375 10607375 single base substitution G T upstream_gene_variant MELA-AU 19 10607794 10607794 single base substitution C T downstream_gene_variant MELA-AU 19 10607794 10607794 single base substitution C T intron_variant MELA-AU 19 10607916 10607916 single base substitution C T downstream_gene_variant MELA-AU 19 10607916 10607916 single base substitution C T intron_variant MELA-AU 19 10608961 10608961 single base substitution C G downstream_gene_variant MELA-AU 19 10608961 10608961 single base substitution C G intron_variant MELA-AU 19 10609454 10609454 single base substitution A C downstream_gene_variant MELA-AU 19 10609454 10609454 single base substitution A C intron_variant MELA-AU 19 10610444 10610444 single base substitution G A intron_variant MELA-AU 19 10610444 10610444 single base substitution G A missense_variant P89L 266C>T MELA-AU 19 10610444 10610444 single base substitution G A upstream_gene_variant MELA-AU 19 10610815 10610815 single base substitution G A intron_variant MELA-AU 19 10610815 10610815 single base substitution G A upstream_gene_variant MELA-AU 19 10611624 10611624 single base substitution G A intron_variant MELA-AU 19 10611624 10611624 single base substitution G A upstream_gene_variant MELA-AU 19 10611703 10611703 single base substitution G A intron_variant MELA-AU 19 10611703 10611703 single base substitution G A upstream_gene_variant MELA-AU 19 10611756 10611756 single base substitution G A intron_variant MELA-AU 19 10611756 10611756 single base substitution G A upstream_gene_variant MELA-AU 19 10612128 10612128 single base substitution A G intron_variant MELA-AU 19 10612128 10612128 single base substitution A G upstream_gene_variant MELA-AU 19 10614347 10614347 single base substitution T A 5_prime_UTR_variant MELA-AU 19 10614347 10614347 single base substitution T A upstream_gene_variant MELA-AU 19 10614442 10614442 single base substitution C T upstream_gene_variant MELA-AU 19 10614597 10614597 single base substitution G A upstream_gene_variant MELA-AU 19 10614980 10614980 single base substitution C T upstream_gene_variant MELA-AU 19 10615976 10615976 single base substitution C T upstream_gene_variant MELA-AU 19 10616788 10616788 single base substitution G A upstream_gene_variant MELA-AU 19 10616842 10616842 single base substitution C T upstream_gene_variant MELA-AU 19 10616981 10616981 single base substitution C T upstream_gene_variant MELA-AU 19 10617082 10617082 single base substitution A G upstream_gene_variant MELA-AU 19 10617411 10617411 single base substitution G A upstream_gene_variant MELA-AU 19 10617735 10617735 single base substitution C T upstream_gene_variant MELA-AU 19 10617746 10617746 single base substitution C T upstream_gene_variant MELA-AU 19 10617899 10617899 single base substitution C T upstream_gene_variant MELA-AU 19 10617993 10617993 single base substitution C T upstream_gene_variant MELA-AU 19 10618166 10618166 single base substitution A G upstream_gene_variant MELA-AU 19 10618180 10618181 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 10618700 10618700 single base substitution C T upstream_gene_variant MELA-AU 19 10618702 10618702 single base substitution C T upstream_gene_variant MELA-AU 19 10618760 10618760 single base substitution C T upstream_gene_variant MELA-AU 19 10618775 10618775 single base substitution C T upstream_gene_variant MELA-AU 19 10618813 10618814 multiple base substitution (>=2bp and <=200bp) TC AT upstream_gene_variant MELA-AU 19 10618827 10618827 single base substitution G A upstream_gene_variant MELA-AU 19 10618926 10618926 single base substitution C T upstream_gene_variant MELA-AU 19 10618969 10618969 single base substitution G A upstream_gene_variant MELA-AU 19 10619028 10619028 single base substitution C T upstream_gene_variant MELA-AU 19 10619093 10619093 single base substitution G A upstream_gene_variant MELA-AU 19 10619123 10619123 single base substitution C T upstream_gene_variant MELA-AU 19 10619258 10619258 single base substitution G A upstream_gene_variant MELA-AU 19 10619333 10619333 single base substitution C T upstream_gene_variant NBL-US 19 10610606 10610607 multiple base substitution (>=2bp and <=200bp) GA AT intron_variant NBL-US 19 10610606 10610607 multiple base substitution (>=2bp and <=200bp) GA AT missense_variant S35I 103TC>AT NBL-US 19 10610606 10610607 multiple base substitution (>=2bp and <=200bp) GA AT upstream_gene_variant ORCA-IN 19 10600447 10600447 single base substitution G A downstream_gene_variant ORCA-IN 19 10600447 10600447 single base substitution G A intron_variant ORCA-IN 19 10600447 10600447 single base substitution G A missense_variant R470C 1408C>T ORCA-IN 19 10600447 10600447 single base substitution G A missense_variant R76C 226C>T ORCA-IN 19 10600447 10600447 single base substitution G A upstream_gene_variant ORCA-IN 19 10602602 10602602 single base substitution G A downstream_gene_variant ORCA-IN 19 10602602 10602602 single base substitution G A missense_variant R326C 976C>T ORCA-IN 19 10602602 10602602 single base substitution G A upstream_gene_variant ORCA-IN 19 10602748 10602748 single base substitution G A 3_prime_UTR_variant ORCA-IN 19 10602748 10602748 single base substitution G A downstream_gene_variant ORCA-IN 19 10602748 10602748 single base substitution G A exon_variant ORCA-IN 19 10602748 10602748 single base substitution G A missense_variant T277M 830C>T ORCA-IN 19 10602748 10602748 single base substitution G A upstream_gene_variant ORCA-IN 19 10603960 10603960 single base substitution G A intron_variant ORCA-IN 19 10603960 10603960 single base substitution G A upstream_gene_variant ORCA-IN 19 10610293 10610293 single base substitution G A intron_variant ORCA-IN 19 10610293 10610293 single base substitution G A synonymous_variant F139F 417C>T ORCA-IN 19 10610293 10610293 single base substitution G A upstream_gene_variant ORCA-IN 19 10610576 10610576 single base substitution G A intron_variant ORCA-IN 19 10610576 10610576 single base substitution G A missense_variant S45F 134C>T ORCA-IN 19 10610576 10610576 single base substitution G A upstream_gene_variant ORCA-IN 19 10615460 10615460 single base substitution G A upstream_gene_variant OV-AU 19 10592356 10592356 single base substitution C T downstream_gene_variant OV-AU 19 10593021 10593021 single base substitution T G downstream_gene_variant OV-AU 19 10598606 10598606 single base substitution A G downstream_gene_variant OV-AU 19 10598606 10598606 single base substitution A G intron_variant OV-AU 19 10600039 10600039 single base substitution A T downstream_gene_variant OV-AU 19 10600039 10600039 single base substitution A T exon_variant OV-AU 19 10600039 10600039 single base substitution A T intron_variant OV-AU 19 10600039 10600039 single base substitution A T missense_variant C513S 1537T>A OV-AU 19 10600861 10600861 single base substitution G T downstream_gene_variant OV-AU 19 10600861 10600861 single base substitution G T intron_variant OV-AU 19 10600861 10600861 single base substitution G T upstream_gene_variant OV-AU 19 10602414 10602414 single base substitution G C downstream_gene_variant OV-AU 19 10602414 10602414 single base substitution G C exon_variant OV-AU 19 10602414 10602414 single base substitution G C synonymous_variant T388T 1164C>G OV-AU 19 10602414 10602414 single base substitution G C upstream_gene_variant OV-AU 19 10603981 10603981 single base substitution C T intron_variant OV-AU 19 10603981 10603981 single base substitution C T upstream_gene_variant OV-AU 19 10604318 10604318 single base substitution A T intron_variant OV-AU 19 10604318 10604318 single base substitution A T upstream_gene_variant OV-AU 19 10613401 10613401 single base substitution T G 5_prime_UTR_variant OV-AU 19 10613401 10613401 single base substitution T G intron_variant OV-AU 19 10613401 10613401 single base substitution T G upstream_gene_variant OV-AU 19 10617378 10617378 single base substitution C G upstream_gene_variant PACA-AU 19 10594518 10594518 single base substitution C G downstream_gene_variant PACA-AU 19 10598447 10598447 single base substitution G A downstream_gene_variant PACA-AU 19 10598447 10598447 single base substitution G A intron_variant PACA-AU 19 10598448 10598448 single base substitution G A downstream_gene_variant PACA-AU 19 10598448 10598448 single base substitution G A intron_variant PACA-AU 19 10599405 10599405 single base substitution G A downstream_gene_variant PACA-AU 19 10599405 10599405 single base substitution G A intron_variant PACA-AU 19 10599926 10599926 single base substitution C T 3_prime_UTR_variant PACA-AU 19 10599926 10599926 single base substitution C T downstream_gene_variant PACA-AU 19 10599926 10599926 single base substitution C T exon_variant PACA-AU 19 10599926 10599926 single base substitution C T intron_variant PACA-AU 19 10599926 10599926 single base substitution C T missense_variant M550I 1650G>A PACA-AU 19 10603920 10603920 single base substitution C T intron_variant PACA-AU 19 10603920 10603920 single base substitution C T upstream_gene_variant PACA-AU 19 10606006 10606006 single base substitution C A downstream_gene_variant PACA-AU 19 10606006 10606006 single base substitution C A intron_variant PACA-AU 19 10606006 10606006 single base substitution C A upstream_gene_variant PACA-AU 19 10614056 10614056 single base substitution G A 5_prime_UTR_variant PACA-AU 19 10614056 10614056 single base substitution G A exon_variant PACA-AU 19 10614056 10614056 single base substitution G A upstream_gene_variant PACA-CA 19 10595942 10595942 single base substitution A G downstream_gene_variant PACA-CA 19 10599472 10599472 single base substitution T A downstream_gene_variant PACA-CA 19 10599472 10599472 single base substitution T A intron_variant PACA-CA 19 10602059 10602059 insertion of <=200bp - C downstream_gene_variant PACA-CA 19 10602059 10602059 insertion of <=200bp - C intron_variant PACA-CA 19 10602059 10602059 insertion of <=200bp - C upstream_gene_variant PACA-CA 19 10602495 10602495 single base substitution C T downstream_gene_variant PACA-CA 19 10602495 10602495 single base substitution C T exon_variant PACA-CA 19 10602495 10602495 single base substitution C T synonymous_variant P361P 1083G>A PACA-CA 19 10602495 10602495 single base substitution C T upstream_gene_variant PACA-CA 19 10603440 10603440 single base substitution T C intron_variant PACA-CA 19 10603440 10603440 single base substitution T C upstream_gene_variant PACA-CA 19 10607192 10607192 single base substitution A G downstream_gene_variant PACA-CA 19 10607192 10607192 single base substitution A G intron_variant PACA-CA 19 10607192 10607192 single base substitution A G upstream_gene_variant PACA-CA 19 10610439 10610439 single base substitution C A intron_variant PACA-CA 19 10610439 10610439 single base substitution C A missense_variant A91S 271G>T PACA-CA 19 10610439 10610439 single base substitution C A upstream_gene_variant PACA-CA 19 10610590 10610590 single base substitution C T intron_variant PACA-CA 19 10610590 10610590 single base substitution C T synonymous_variant A40A 120G>A PACA-CA 19 10610590 10610590 single base substitution C T upstream_gene_variant PACA-CA 19 10612292 10612292 single base substitution C G intron_variant PACA-CA 19 10612292 10612292 single base substitution C G upstream_gene_variant PACA-CA 19 10613957 10613957 single base substitution G A 5_prime_UTR_variant PACA-CA 19 10613957 10613957 single base substitution G A exon_variant PACA-CA 19 10613957 10613957 single base substitution G A upstream_gene_variant PACA-CA 19 10615389 10615389 single base substitution C T upstream_gene_variant PACA-CA 19 10615460 10615460 single base substitution G A upstream_gene_variant PACA-CA 19 10616849 10616849 single base substitution T C upstream_gene_variant PACA-CA 19 10619309 10619309 single base substitution G A upstream_gene_variant PAEN-AU 19 10613808 10613808 single base substitution T G 5_prime_UTR_variant PAEN-AU 19 10613808 10613808 single base substitution T G intron_variant PAEN-AU 19 10613808 10613808 single base substitution T G upstream_gene_variant PBCA-DE 19 10597892 10597892 single base substitution C T downstream_gene_variant PBCA-DE 19 10597892 10597892 single base substitution C T intron_variant PBCA-DE 19 10599287 10599287 insertion of <=200bp - A downstream_gene_variant PBCA-DE 19 10599287 10599287 insertion of <=200bp - A intron_variant PBCA-DE 19 10601151 10601151 single base substitution C T downstream_gene_variant PBCA-DE 19 10601151 10601151 single base substitution C T intron_variant PBCA-DE 19 10601151 10601151 single base substitution C T upstream_gene_variant PBCA-DE 19 10612315 10612315 insertion of <=200bp - A intron_variant PBCA-DE 19 10612315 10612315 insertion of <=200bp - A upstream_gene_variant PBCA-DE 19 10612434 10612434 single base substitution G A intron_variant PBCA-DE 19 10612434 10612434 single base substitution G A upstream_gene_variant PBCA-DE 19 10619031 10619031 single base substitution G A upstream_gene_variant PRAD-CA 19 10597920 10597920 single base substitution G C downstream_gene_variant PRAD-CA 19 10597920 10597920 single base substitution G C intron_variant PRAD-CA 19 10618408 10618408 single base substitution C T upstream_gene_variant PRAD-UK 19 10594338 10594338 deletion of <=200bp T - downstream_gene_variant PRAD-UK 19 10596412 10596412 single base substitution G C downstream_gene_variant PRAD-UK 19 10618904 10618904 single base substitution G T upstream_gene_variant PRAD-US 19 10597450 10597450 single base substitution C T 3_prime_UTR_variant PRAD-US 19 10597450 10597450 single base substitution C T exon_variant PRAD-US 19 10597450 10597450 single base substitution C T missense_variant D132N 394G>A PRAD-US 19 10597450 10597450 single base substitution C T missense_variant D585N 1753G>A PRAD-US 19 10602358 10602358 single base substitution G A downstream_gene_variant PRAD-US 19 10602358 10602358 single base substitution G A exon_variant PRAD-US 19 10602358 10602358 single base substitution G A missense_variant A13V 38C>T PRAD-US 19 10602358 10602358 single base substitution G A missense_variant A407V 1220C>T PRAD-US 19 10602358 10602358 single base substitution G A upstream_gene_variant PRAD-US 19 10602517 10602517 single base substitution C A downstream_gene_variant PRAD-US 19 10602517 10602517 single base substitution C A exon_variant PRAD-US 19 10602517 10602517 single base substitution C A missense_variant R354L 1061G>T PRAD-US 19 10602517 10602517 single base substitution C A upstream_gene_variant READ-US 19 10600463 10600463 single base substitution G A downstream_gene_variant READ-US 19 10600463 10600463 single base substitution G A intron_variant READ-US 19 10600463 10600463 single base substitution G A synonymous_variant G464G 1392C>T READ-US 19 10600463 10600463 single base substitution G A synonymous_variant G70G 210C>T READ-US 19 10600463 10600463 single base substitution G A upstream_gene_variant READ-US 19 10610212 10610212 single base substitution G A exon_variant READ-US 19 10610212 10610212 single base substitution G A synonymous_variant S166S 498C>T READ-US 19 10610212 10610212 single base substitution G A upstream_gene_variant RECA-EU 19 10607192 10607192 single base substitution A G downstream_gene_variant RECA-EU 19 10607192 10607192 single base substitution A G intron_variant RECA-EU 19 10607192 10607192 single base substitution A G upstream_gene_variant RECA-EU 19 10611234 10611234 single base substitution C G intron_variant RECA-EU 19 10611234 10611234 single base substitution C G upstream_gene_variant RECA-EU 19 10612692 10612692 single base substitution G C intron_variant RECA-EU 19 10612692 10612692 single base substitution G C upstream_gene_variant SKCA-BR 19 10593826 10593827 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 19 10595519 10595519 single base substitution G A downstream_gene_variant SKCA-BR 19 10599685 10599685 single base substitution G A downstream_gene_variant SKCA-BR 19 10599685 10599685 single base substitution G A intron_variant SKCA-BR 19 10600145 10600145 single base substitution T C downstream_gene_variant SKCA-BR 19 10600145 10600145 single base substitution T C intron_variant SKCA-BR 19 10600145 10600145 single base substitution T C upstream_gene_variant SKCA-BR 19 10600923 10600923 single base substitution A G downstream_gene_variant SKCA-BR 19 10600923 10600923 single base substitution A G intron_variant SKCA-BR 19 10600923 10600923 single base substitution A G upstream_gene_variant SKCA-BR 19 10603874 10603874 single base substitution G A intron_variant SKCA-BR 19 10603874 10603874 single base substitution G A upstream_gene_variant SKCA-BR 19 10605162 10605162 single base substitution A C downstream_gene_variant SKCA-BR 19 10605162 10605162 single base substitution A C intron_variant SKCA-BR 19 10605162 10605162 single base substitution A C upstream_gene_variant SKCA-BR 19 10605333 10605334 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 19 10605333 10605334 deletion of <=200bp CT - intron_variant SKCA-BR 19 10605333 10605334 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 19 10608962 10608962 single base substitution A C downstream_gene_variant SKCA-BR 19 10608962 10608962 single base substitution A C intron_variant SKCA-BR 19 10611357 10611358 deletion of <=200bp CT - intron_variant SKCA-BR 19 10611357 10611358 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 19 10612253 10612253 single base substitution C T intron_variant SKCA-BR 19 10612253 10612253 single base substitution C T upstream_gene_variant SKCA-BR 19 10613057 10613057 single base substitution A C intron_variant SKCA-BR 19 10613057 10613057 single base substitution A C upstream_gene_variant SKCA-BR 19 10613900 10613900 single base substitution G A intron_variant SKCA-BR 19 10613900 10613900 single base substitution G A upstream_gene_variant SKCA-BR 19 10614042 10614042 single base substitution A G 5_prime_UTR_variant SKCA-BR 19 10614042 10614042 single base substitution A G exon_variant SKCA-BR 19 10614042 10614042 single base substitution A G upstream_gene_variant SKCA-BR 19 10614066 10614066 single base substitution A G 5_prime_UTR_variant SKCA-BR 19 10614066 10614066 single base substitution A G exon_variant SKCA-BR 19 10614066 10614066 single base substitution A G upstream_gene_variant SKCA-BR 19 10614342 10614345 deletion of <=200bp TTTC - 5_prime_UTR_variant SKCA-BR 19 10614342 10614345 deletion of <=200bp TTTC - upstream_gene_variant SKCA-BR 19 10616801 10616801 single base substitution G A upstream_gene_variant SKCA-BR 19 10616883 10616883 single base substitution G A upstream_gene_variant SKCM-US 19 10600376 10600376 single base substitution C T downstream_gene_variant SKCM-US 19 10600376 10600376 single base substitution C T intron_variant SKCM-US 19 10600376 10600376 single base substitution C T synonymous_variant E493E 1479G>A SKCM-US 19 10600376 10600376 single base substitution C T synonymous_variant E99E 297G>A SKCM-US 19 10600376 10600376 single base substitution C T upstream_gene_variant SKCM-US 19 10600447 10600447 single base substitution G A downstream_gene_variant SKCM-US 19 10600447 10600447 single base substitution G A intron_variant SKCM-US 19 10600447 10600447 single base substitution G A missense_variant R470C 1408C>T SKCM-US 19 10600447 10600447 single base substitution G A missense_variant R76C 226C>T SKCM-US 19 10600447 10600447 single base substitution G A upstream_gene_variant SKCM-US 19 10610321 10610321 single base substitution G A intron_variant SKCM-US 19 10610321 10610321 single base substitution G A missense_variant P130L 389C>T SKCM-US 19 10610321 10610321 single base substitution G A upstream_gene_variant SKCM-US 19 10610578 10610578 single base substitution G A intron_variant SKCM-US 19 10610578 10610578 single base substitution G A synonymous_variant P44P 132C>T SKCM-US 19 10610578 10610578 single base substitution G A upstream_gene_variant STAD-US 19 10599954 10599954 single base substitution G A 3_prime_UTR_variant STAD-US 19 10599954 10599954 single base substitution G A downstream_gene_variant STAD-US 19 10599954 10599954 single base substitution G A exon_variant STAD-US 19 10599954 10599954 single base substitution G A intron_variant STAD-US 19 10599954 10599954 single base substitution G A missense_variant T541I 1622C>T STAD-US 19 10599967 10599967 single base substitution A G 3_prime_UTR_variant STAD-US 19 10599967 10599967 single base substitution A G downstream_gene_variant STAD-US 19 10599967 10599967 single base substitution A G exon_variant STAD-US 19 10599967 10599967 single base substitution A G intron_variant STAD-US 19 10599967 10599967 single base substitution A G missense_variant Y537H 1609T>C STAD-US 19 10602646 10602646 single base substitution T C downstream_gene_variant STAD-US 19 10602646 10602646 single base substitution T C exon_variant STAD-US 19 10602646 10602646 single base substitution T C missense_variant H311R 932A>G STAD-US 19 10602646 10602646 single base substitution T C upstream_gene_variant STAD-US 19 10602716 10602716 single base substitution A G 3_prime_UTR_variant STAD-US 19 10602716 10602716 single base substitution A G downstream_gene_variant STAD-US 19 10602716 10602716 single base substitution A G exon_variant STAD-US 19 10602716 10602716 single base substitution A G missense_variant C288R 862T>C STAD-US 19 10602716 10602716 single base substitution A G upstream_gene_variant STAD-US 19 10602832 10602832 single base substitution C T 3_prime_UTR_variant STAD-US 19 10602832 10602832 single base substitution C T downstream_gene_variant STAD-US 19 10602832 10602832 single base substitution C T exon_variant STAD-US 19 10602832 10602832 single base substitution C T missense_variant C249Y 746G>A STAD-US 19 10602832 10602832 single base substitution C T upstream_gene_variant STAD-US 19 10602938 10602938 single base substitution C T missense_variant V214M 640G>A STAD-US 19 10602938 10602938 single base substitution C T splice_region_variant STAD-US 19 10602938 10602938 single base substitution C T upstream_gene_variant STAD-US 19 10610092 10610092 single base substitution G A 3_prime_UTR_variant STAD-US 19 10610092 10610092 single base substitution G A exon_variant STAD-US 19 10610092 10610092 single base substitution G A synonymous_variant Y206Y 618C>T STAD-US 19 10610266 10610266 single base substitution G A splice_region_variant STAD-US 19 10610266 10610266 single base substitution G A synonymous_variant G148G 444C>T STAD-US 19 10610266 10610266 single base substitution G A upstream_gene_variant STAD-US 19 10610425 10610425 single base substitution G T intron_variant STAD-US 19 10610425 10610425 single base substitution G T synonymous_variant A95A 285C>A STAD-US 19 10610425 10610425 single base substitution G T upstream_gene_variant STAD-US 19 10610476 10610476 single base substitution G A intron_variant STAD-US 19 10610476 10610476 single base substitution G A synonymous_variant D78D 234C>T STAD-US 19 10610476 10610476 single base substitution G A upstream_gene_variant STAD-US 19 10610561 10610561 single base substitution C T intron_variant STAD-US 19 10610561 10610561 single base substitution C T missense_variant R50H 149G>A STAD-US 19 10610561 10610561 single base substitution C T upstream_gene_variant STAD-US 19 10610576 10610576 single base substitution G A intron_variant STAD-US 19 10610576 10610576 single base substitution G A missense_variant S45F 134C>T STAD-US 19 10610576 10610576 single base substitution G A upstream_gene_variant STAD-US 19 10610610 10610610 single base substitution C T intron_variant STAD-US 19 10610610 10610610 single base substitution C T missense_variant A34T 100G>A STAD-US 19 10610610 10610610 single base substitution C T upstream_gene_variant STAD-US 19 10610652 10610652 single base substitution G A intron_variant STAD-US 19 10610652 10610652 single base substitution G A stop_gained Q20* 58C>T STAD-US 19 10610652 10610652 single base substitution G A upstream_gene_variant THCA-SA 19 10610236 10610236 single base substitution A G exon_variant THCA-SA 19 10610236 10610236 single base substitution A G synonymous_variant G158G 474T>C THCA-SA 19 10610236 10610236 single base substitution A G upstream_gene_variant THCA-US 19 10600426 10600426 single base substitution C T downstream_gene_variant THCA-US 19 10600426 10600426 single base substitution C T intron_variant THCA-US 19 10600426 10600426 single base substitution C T missense_variant G477S 1429G>A THCA-US 19 10600426 10600426 single base substitution C T missense_variant G83S 247G>A THCA-US 19 10600426 10600426 single base substitution C T upstream_gene_variant UCEC-US 19 10600021 10600021 insertion of <=200bp - A downstream_gene_variant UCEC-US 19 10600021 10600021 insertion of <=200bp - A exon_variant UCEC-US 19 10600021 10600021 insertion of <=200bp - A frameshift_variant I519I? UCEC-US 19 10600021 10600021 insertion of <=200bp - A intron_variant UCEC-US 19 10600391 10600391 single base substitution C A downstream_gene_variant UCEC-US 19 10600391 10600391 single base substitution C A intron_variant UCEC-US 19 10600391 10600391 single base substitution C A missense_variant E488D 1464G>T UCEC-US 19 10600391 10600391 single base substitution C A missense_variant E94D 282G>T UCEC-US 19 10600391 10600391 single base substitution C A upstream_gene_variant UCEC-US 19 10602314 10602314 single base substitution C T downstream_gene_variant UCEC-US 19 10602314 10602314 single base substitution C T exon_variant UCEC-US 19 10602314 10602314 single base substitution C T missense_variant D28N 82G>A UCEC-US 19 10602314 10602314 single base substitution C T missense_variant D422N 1264G>A UCEC-US 19 10602314 10602314 single base substitution C T upstream_gene_variant UCEC-US 19 10602601 10602601 single base substitution C T downstream_gene_variant UCEC-US 19 10602601 10602601 single base substitution C T missense_variant R326H 977G>A UCEC-US 19 10602601 10602601 single base substitution C T upstream_gene_variant UCEC-US 19 10610156 10610156 single base substitution A G 3_prime_UTR_variant UCEC-US 19 10610156 10610156 single base substitution A G exon_variant UCEC-US 19 10610156 10610156 single base substitution A G missense_variant I185T 554T>C UCEC-US 19 10610205 10610205 single base substitution G A exon_variant UCEC-US 19 10610205 10610205 single base substitution G A missense_variant R169C 505C>T UCEC-US 19 10610205 10610205 single base substitution G A upstream_gene_variant UCEC-US 19 10610218 10610218 single base substitution G A exon_variant UCEC-US 19 10610218 10610218 single base substitution G A synonymous_variant I164I 492C>T UCEC-US 19 10610218 10610218 single base substitution G A upstream_gene_variant UCEC-US 19 10610427 10610427 single base substitution C T intron_variant UCEC-US 19 10610427 10610427 single base substitution C T missense_variant A95T 283G>A UCEC-US 19 10610427 10610427 single base substitution C T upstream_gene_variant UCEC-US 19 10610561 10610561 single base substitution C T intron_variant UCEC-US 19 10610561 10610561 single base substitution C T missense_variant R50H 149G>A UCEC-US 19 10610561 10610561 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand MOLT-4 COSM180623 c.1607G>A p.R536H Substitution - Missense 19:10489293-10489293 - TCGA-D3-A2J7-06 COSM3528285 c.389C>T p.P130L Substitution - Missense 19:10499645-10499645 - TCGA-BR-4257-01 COSM4073870 c.618C>T p.Y206Y Substitution - coding silent 19:10499416-10499416 - RMS105_ COSM4986189 c.60G>T p.Q20H Substitution - Missense 19:10499974-10499974 - TCGA-EW-A1J5-01 COSM564844 c.1345G>T p.E449* Substitution - Nonsense 19:10489834-10489834 - ccRCC-34 COSM1659324 c.1752delC p.Y584fs*1 Deletion - Frameshift 19:10486775-10486775 - ESCC_BICR_063T COSM564847 c.1408C>T p.R470C Substitution - Missense 19:10489771-10489771 - BCB301T COSM4925833 c.811G>T p.V271L Substitution - Missense 19:10492091-10492091 - 86506 COSM94571 c.1252G>A p.V418M Substitution - Missense 19:10491650-10491650 - TCGA-ED-A4XI-01 COSM4913158 c.1574A>G p.Y525C Substitution - Missense 19:10489326-10489326 - 435 COSM4433833 c.403C>T p.R135C Substitution - Missense 19:10499631-10499631 - TCGA-66-2754-01 COSM710202 c.1632G>T p.W544C Substitution - Missense 19:10489268-10489268 - Pa34X COSM84486 c.1284C>T p.V428V Substitution - coding silent 19:10491618-10491618 - MEL-Ma-Mel-59 COSM1167868 c.904_905insG p.V302fs*48 Insertion - Frameshift 19:10491997-10491998 - LUAD-YINHD COSM349505 c.1255G>T p.G419W Substitution - Missense 19:10491647-10491647 - TCGA-BJ-A192-01 COSM3371136 c.1429G>A p.G477S Substitution - Missense 19:10489750-10489750 - RK028_C01 COSM3742714 c.1379G>T p.R460M Substitution - Missense 19:10489800-10489800 - SH-7329 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - CHC2128T COSM2812613 c.990C>T p.T330T Substitution - coding silent 19:10491912-10491912 - DM55 COSM5609242 c.1413C>T p.L471L Substitution - coding silent 19:10489766-10489766 - 1409_T COSM3959487 c.218G>T p.S73I Substitution - Missense 19:10499816-10499816 - TCGA-G2-A3IE-01 COSM1303938 c.948G>A p.V316V Substitution - coding silent 19:10491954-10491954 - PCSI_0056_Pa_X COSM3378602 c.271G>T p.A91S Substitution - Missense 19:10499763-10499763 - KYSE-180 COSM2812621 c.833C>A p.P278Q Substitution - Missense 19:10492069-10492069 - TCGA-AA-A00N-01 COSM275664 c.1674G>A p.G558G Substitution - coding silent 19:10489226-10489226 - LUAD-S01381 COSM398498 c.287A>T p.H96L Substitution - Missense 19:10499747-10499747 - LUAD-S01306 COSM392394 c.1189_1191delAAC p.N397delN Deletion - In frame 19:10491711-10491713 - TCGA-66-2773-01 COSM564847 c.1408C>T p.R470C Substitution - Missense 19:10489771-10489771 - TCGA-51-4081-01 COSM710197 c.1252G>T p.V418L Substitution - Missense 19:10491650-10491650 - ESO-H63 COSM1255509 c.970G>A p.V324M Substitution - Missense 19:10491932-10491932 - SC_9084 COSM5572552 c.899A>G p.Y300C Substitution - Missense 19:10492003-10492003 - 101037 COSM96323 c.1666G>T p.A556S Substitution - Missense 19:10489234-10489234 - HCC163 COSM3718031 c.140A>G p.H47R Substitution - Missense 19:10499894-10499894 - SNU-175 COSM2812653 c.129G>A p.T43T Substitution - coding silent 19:10499905-10499905 - HCC082T COSM5816316 c.1460C>A p.A487D Substitution - Missense 19:10489719-10489719 - 112479 COSM94575 c.161A>G p.Y54C Substitution - Missense 19:10499873-10499873 - LUAD-RT-S01721 COSM380449 c.422A>T p.Y141F Substitution - Missense 19:10499612-10499612 - ESCC_BICR_039T COSM710198 c.1264G>A p.D422N Substitution - Missense 19:10491638-10491638 - CHC1205T COSM4951076 c.1803G>C p.R601R Substitution - coding silent 19:10486724-10486724 - CHC1205T COSM4951076 c.1803G>C p.R601R Substitution - coding silent 19:10486724-10486724 - 112415 COSM94574 c.422A>G p.Y141C Substitution - Missense 19:10499612-10499612 - OSCC-GB_01070111 COSM564847 c.1408C>T p.R470C Substitution - Missense 19:10489771-10489771 - LUAD-NYU739 COSM392053 c.1761_1762insT p.T588fs*31 Insertion - Frameshift 19:10486765-10486766 - LUAD-RT-S01818 COSM383936 c.958_959CG>TA p.R320>? Complex 19:10491943-10491944 - CME_0001_Pa_C COSM3378602 c.271G>T p.A91S Substitution - Missense 19:10499763-10499763 - TCGA-18-5595-01 COSM710192 c.779G>A p.R260Q Substitution - Missense 19:10492123-10492123 - HCC174T COSM3718030 c.742G>A p.A248T Substitution - Missense 19:10492160-10492160 - HCC109T COSM5816784 c.821A>G p.H274R Substitution - Missense 19:10492081-10492081 - TCGA-BR-7851-01 COSM4073875 c.58C>T p.Q20* Substitution - Nonsense 19:10499976-10499976 - BCM617T COSM5347239 c.988_989delAC p.T330fs*19 Deletion - Frameshift 19:10491913-10491914 - TCGA-A3-3324-01 COSM1136093 c.160T>G p.Y54D Substitution - Missense 19:10499874-10499874 - 273T COSM1727613 c.523delC p.L175fs*55 Deletion - Frameshift 19:10499511-10499511 - ESCC_129 COSM5641836 c.1527G>T p.G509G Substitution - coding silent 19:10489652-10489652 - HCC1008 COSM32539 c.68G>A p.C23Y Substitution - Missense 19:10499966-10499966 - BN32 COSM1611495 c.187G>A p.A63T Substitution - Missense 19:10499847-10499847 - TCGA-AA-3715-01 COSM269429 c.373A>G p.I125V Substitution - Missense 19:10499661-10499661 - B65-Tumor COSM3932863 c.1611C>T p.Y537Y Substitution - coding silent 19:10489289-10489289 - UMC11 COSM2812591 c.1712G>C p.G571A Substitution - Missense 19:10486815-10486815 - HCC123T COSM2812618 c.880G>T p.D294Y Substitution - Missense 19:10492022-10492022 - TCGA-46-6025-01 COSM710186 c.223C>T p.Q75* Substitution - Nonsense 19:10499811-10499811 - J10_T COSM3959483 c.1447C>A p.R483S Substitution - Missense 19:10489732-10489732 - SH-9771 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - 4132_T COSM3959488 c.134C>A p.S45Y Substitution - Missense 19:10499900-10499900 - TCGA-37-4133-01 COSM710191 c.728C>G p.S243C Substitution - Missense 19:10492174-10492174 - 13681 COSM5264513 c.994G>T p.G332C Substitution - Missense 19:10491908-10491908 - CHC2200T COSM1524062 c.958C>T p.R320W Substitution - Missense 19:10491944-10491944 - TCGA-AX-A063-01 COSM990605 c.554T>C p.I185T Substitution - Missense 19:10499480-10499480 - 8052577 COSM3388547 c.1650G>A p.M550I Substitution - Missense 19:10489250-10489250 - RK216_C01 COSM1524066 c.1661G>A p.R554Q Substitution - Missense 19:10489239-10489239 - HCC152 COSM3718043 c.1113C>T p.G371G Substitution - coding silent 19:10491789-10491789 - TCGA-EJ-A46G-01 COSM3783169 c.1061G>T p.R354L Substitution - Missense 19:10491841-10491841 - 2011-2300:2012-321-T COSM2812636 c.556G>A p.G186S Substitution - Missense 19:10499478-10499478 - Pat_16_A COSM4590889 c.457C>T p.L153F Substitution - Missense 19:10499577-10499577 - YURTHE COSM1711812 c.1423G>C p.V475L Substitution - Missense 19:10489756-10489756 - ccRCC-51 COSM1659425 c.761A>C p.K254T Substitution - Missense 19:10492141-10492141 - SH-1439 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - LU-1991 COSM5614594 c.1306C>A p.H436N Substitution - Missense 19:10491596-10491596 - CSCC-19-T COSM4456087 c.454_455GT>AA p.V152N Substitution - Missense 19:10499579-10499580 - LUAD-D01603 COSM337518 c.330G>A p.M110I Substitution - Missense 19:10499704-10499704 - TCGA-18-3409-01 COSM710194 c.953C>T p.P318L Substitution - Missense 19:10491949-10491949 - LUAD-AEIUF COSM404900 c.946_951delGTGATG p.V316_M317delVM Deletion - In frame 19:10491951-10491956 - BCB301T COSM4925833 c.811G>T p.V271L Substitution - Missense 19:10492091-10492091 - TCGA-60-2722-01 COSM710199 c.1438G>T p.G480W Substitution - Missense 19:10489741-10489741 - TCGA-D1-A103-01 COSM990604 c.977G>A p.R326H Substitution - Missense 19:10491925-10491925 - ESCC_BICR_033T COSM1524059 c.811G>A p.V271M Substitution - Missense 19:10492091-10492091 - PD7217a COSM5791857 c.158G>T p.S53I Substitution - Missense 19:10499876-10499876 - TCGA-39-5031-01 COSM710185 c.44G>T p.R15L Substitution - Missense 19:10499990-10499990 - S01516 COSM5669062 c.701G>C p.R234P Substitution - Missense 19:10492201-10492201 - TCGA-CD-8536-01 COSM4073868 c.746G>A p.C249Y Substitution - Missense 19:10492156-10492156 - CHC1616T COSM4951265 c.212G>A p.R71Q Substitution - Missense 19:10499822-10499822 - TCGA-CH-5792-01 COSM1130008 c.1220C>T p.A407V Substitution - Missense 19:10491682-10491682 - LUAD-U6SJ7 COSM400196 c.1801C>T p.R601W Substitution - Missense 19:10486726-10486726 - 107586 COSM95977 c.246G>A p.Q82Q Substitution - coding silent 19:10499788-10499788 - TCGA-AN-A046-01 COSM1390137 c.493G>A p.D165N Substitution - Missense 19:10499541-10499541 - LN18 COSM5712866 c.715G>A p.V239M Substitution - Missense 19:10492187-10492187 - DM79 COSM5609245 c.750C>T p.I250I Substitution - coding silent 19:10492152-10492152 - HCC39 COSM1611494 c.722G>A p.C241Y Substitution - Missense 19:10492180-10492180 - BD236T COSM5519603 c.942G>A p.T314T Substitution - coding silent 19:10491960-10491960 - CHC798T COSM4950717 c.1186_1187insC p.Y396fs*19 Insertion - Frameshift 19:10491715-10491716 - SH-9161 COSM3932863 c.1611C>T p.Y537Y Substitution - coding silent 19:10489289-10489289 - TCGA-AM-5821-01 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - LUAD-NYU284 COSM372918 c.850C>T p.Q284* Substitution - Nonsense 19:10492052-10492052 - PD12803a COSM990607 c.492C>T p.I164I Substitution - coding silent 19:10499542-10499542 - AOCS-090-1-0 COSM4140211 c.1164C>G p.T388T Substitution - coding silent 19:10491738-10491738 - HCC158T COSM3665412 c.747delC p.C249fs*1 Deletion - Frameshift 19:10492155-10492155 - OSCC-GB_00600111 COSM4890280 c.417C>T p.F139F Substitution - coding silent 19:10499617-10499617 - DM28 COSM5609243 c.438C>T p.S146S Substitution - coding silent 19:10499596-10499596 - SH-3327 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - TCGA-60-2710-01 COSM564847 c.1408C>T p.R470C Substitution - Missense 19:10489771-10489771 - TCGA-18-5595-01 COSM710200 c.1479G>C p.E493D Substitution - Missense 19:10489700-10489700 - LUAD-RT-S01840 COSM384772 c.1833G>C p.E611D Substitution - Missense 19:10486694-10486694 - TCGA-22-4599-01 COSM710187 c.463G>T p.V155F Substitution - Missense 19:10499571-10499571 - 86568 COSM95621 c.1006C>T p.R336* Substitution - Nonsense 19:10491896-10491896 - 193T COSM1524057 c.706G>A p.D236N Substitution - Missense 19:10492196-10492196 - TCGA-21-1077-01 COSM710198 c.1264G>A p.D422N Substitution - Missense 19:10491638-10491638 - AOCS-080-1-9 COSM4140210 c.1537T>A p.C513S Substitution - Missense 19:10489363-10489363 - TCGA-B0-4815-01 COSM474127 c.1630T>C p.W544R Substitution - Missense 19:10489270-10489270 - NCI-H23 COSM1196320 c.579G>C p.Q193H Substitution - Missense 19:10499455-10499455 - RMS110_ COSM4987166 c.247G>A p.V83I Substitution - Missense 19:10499787-10499787 - TCGA-F5-6814-01 COSM3422379 c.498C>T p.S166S Substitution - coding silent 19:10499536-10499536 - A549 COSM1193323 c.997G>T p.G333C Substitution - Missense 19:10491905-10491905 - OSCC-GB_01070111 COSM4889408 c.830C>T p.T277M Substitution - Missense 19:10492072-10492072 - S04-45633-TP COSM4991204 c.726G>A p.E242E Substitution - coding silent 19:10492176-10492176 - SH-7282 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - TCGA-BG-A18B-01 COSM990607 c.492C>T p.I164I Substitution - coding silent 19:10499542-10499542 - HCC163T COSM3718031 c.140A>G p.H47R Substitution - Missense 19:10499894-10499894 - MedB-1 COSM5621093 c.883T>C p.S295P Substitution - Missense 19:10492019-10492019 - LC_S3 COSM1189872 c.1663A>T p.S555C Substitution - Missense 19:10489237-10489237 - H322T COSM1195038 c.1380G>T p.R460S Substitution - Missense 19:10489799-10489799 - CHC1592T COSM4949875 c.1626_1627delGA p.E542fs*31 Deletion - Frameshift 19:10489273-10489274 - BD72T COSM5513458 c.976C>T p.R326C Substitution - Missense 19:10491926-10491926 - CHC1592T COSM4949875 c.1626_1627delGA p.E542fs*31 Deletion - Frameshift 19:10489273-10489274 - T3021 COSM4695085 c.1628C>T p.T543M Substitution - Missense 19:10489272-10489272 - CHC2200T COSM1524062 c.958C>T p.R320W Substitution - Missense 19:10491944-10491944 - CHC301T COSM250998 c.1777G>T p.E593* Substitution - Nonsense 19:10486750-10486750 - ESCC_72 COSM5634314 c.452G>A p.C151Y Substitution - Missense 19:10499582-10499582 - TCGA-BR-6452-01 COSM4073873 c.134C>T p.S45F Substitution - Missense 19:10499900-10499900 - HCC2998 COSM1680643 c.793C>T p.Q265* Substitution - Nonsense 19:10492109-10492109 - TCGA-39-5036-01 COSM564843 c.1268G>T p.G423V Substitution - Missense 19:10491634-10491634 - ESCC-216T COSM94568 c.1715A>G p.Y572C Substitution - Missense 19:10486812-10486812 - 172T COSM1725916 c.340G>T p.G114W Substitution - Missense 19:10499694-10499694 - T22 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - OSCC-GB_01370111 COSM5513458 c.976C>T p.R326C Substitution - Missense 19:10491926-10491926 - LUAD-NYU1021 COSM368093 c.815G>C p.R272P Substitution - Missense 19:10492087-10492087 - SC_9008 COSM5554506 c.31G>A p.G11R Substitution - Missense 19:10500003-10500003 - 13681 COSM5616949 c.993G>T p.A331A Substitution - coding silent 19:10491909-10491909 - BB20T COSM32809 c.1565C>T p.A522V Substitution - Missense 19:10489335-10489335 - DM29 COSM5609244 c.1439G>A p.G480E Substitution - Missense 19:10489740-10489740 - T263 COSM3787539 c.120G>A p.A40A Substitution - coding silent 19:10499914-10499914 - SH-8559 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - ESCC_44 COSM2812630 c.655G>C p.E219Q Substitution - Missense 19:10492247-10492247 - 222 COSM564846 c.1408C>A p.R470S Substitution - Missense 19:10489771-10489771 - HCC152T COSM3718043 c.1113C>T p.G371G Substitution - coding silent 19:10491789-10491789 - TCGA-G3-A3CK-01 COSM4922491 c.312C>A p.S104R Substitution - Missense 19:10499722-10499722 - S02299 COSM5690388 c.1671G>T p.L557L Substitution - coding silent 19:10489229-10489229 - SH-9771 COSM5020974 c.1437C>T p.D479D Substitution - coding silent 19:10489742-10489742 - SNU-C4 COSM4653017 c.399G>A p.M133I Substitution - Missense 19:10499635-10499635 - RK030_C01 COSM3701407 c.1103G>A p.C368Y Substitution - Missense 19:10491799-10491799 - TCGA-33-4538-01 COSM710193 c.929T>C p.L310P Substitution - Missense 19:10491973-10491973 - S02273 COSM5681736 c.587G>T p.C196F Substitution - Missense 19:10499447-10499447 - TCGA-60-2723-01 COSM710190 c.691C>G p.L231V Substitution - Missense 19:10492211-10492211 - GC8_T COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - SH-0348 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - SH-6055 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - TCGA-JW-A5VK-01 COSM4855177 c.700C>T p.R234W Substitution - Missense 19:10492202-10492202 - 2011-2286:2012-1321-T COSM1524062 c.958C>T p.R320W Substitution - Missense 19:10491944-10491944 - SH-9248 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - TCGA-43-6143-01 COSM710201 c.1516A>G p.I506V Substitution - Missense 19:10489663-10489663 - 2011-2338:2012-306-T COSM4604203 c.1250G>T p.G417V Substitution - Missense 19:10491652-10491652 - HN_62995 COSM128306 c.846G>A p.Q282Q Substitution - coding silent 19:10492056-10492056 - TCGA-D1-A103-01 COSM990608 c.283G>A p.A95T Substitution - Missense 19:10499751-10499751 - TCGA-G2-A2EJ-01 COSM96325 c.652G>C p.E218Q Substitution - Missense 19:10492250-10492250 - ccRCC-15 COSM1662411 c.1330G>T p.E444* Substitution - Nonsense 19:10489849-10489849 - TCGA-DD-A4NR-01 COSM4941180 c.410T>C p.I137T Substitution - Missense 19:10499624-10499624 - TCGA-37-5819-01 COSM710199 c.1438G>T p.G480W Substitution - Missense 19:10489741-10489741 - PTC-7C COSM4131169 c.474T>C p.G158G Substitution - coding silent 19:10499560-10499560 - LUAD-RT-S01700 COSM378705 c.212G>T p.R71L Substitution - Missense 19:10499822-10499822 - OSCC-GB_01290111 COSM4073873 c.134C>T p.S45F Substitution - Missense 19:10499900-10499900 - 24T COSM5575724 c.472G>A p.G158S Substitution - Missense 19:10499562-10499562 - LC_C8 COSM1189874 c.554T>A p.I185N Substitution - Missense 19:10499480-10499480 - CHC1737T COSM4951275 c.1136G>A p.G379D Substitution - Missense 19:10491766-10491766 - SC_9076 COSM5553320 c.1029G>A p.E343E Substitution - coding silent 19:10491873-10491873 - TCGA-CG-4300-01 COSM4073871 c.285C>A p.A95A Substitution - coding silent 19:10499749-10499749 - CHC1152T COSM4949871 c.1326-2A>T p.? Unknown 19:10489855-10489855 - PD9702a COSM5794003 c.175C>T p.H59Y Substitution - Missense 19:10499859-10499859 - 12924 COSM5614595 c.288C>G p.H96Q Substitution - Missense 19:10499746-10499746 - 2011-2306:2012-1324-T COSM4606146 c.93G>A p.V31V Substitution - coding silent 19:10499941-10499941 - H23 COSM1196320 c.579G>C p.Q193H Substitution - Missense 19:10499455-10499455 - TCGA-CG-5721-01 COSM4073867 c.862T>C p.C288R Substitution - Missense 19:10492040-10492040 - CHC301T COSM250998 c.1777G>T p.E593* Substitution - Nonsense 19:10486750-10486750 - TCGA-DM-A1DB-01 COSM1390139 c.24C>T p.S8S Substitution - coding silent 19:10500010-10500010 - TCGA-CD-A4MG-01 COSM4073869 c.640G>A p.V214M Substitution - Missense 19:10492262-10492262 - SH-1679 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - COLO320-DM COSM2812640 c.471C>T p.N157N Substitution - coding silent 19:10499563-10499563 - EGC15 COSM5056181 c.570C>T p.F190F Substitution - coding silent 19:10499464-10499464 - TCGA-BP-4973-01 COSM474129 c.315T>C p.P105P Substitution - coding silent 19:10499719-10499719 - LUAD-NYU1051S COSM368688 c.1807G>T p.G603W Substitution - Missense 19:10486720-10486720 - P51 COSM328699 c.314delC p.P105fs*52 Deletion - Frameshift 19:10499720-10499720 - TCGA-AP-A0LM-01 COSM710198 c.1264G>A p.D422N Substitution - Missense 19:10491638-10491638 - 1848_T COSM3959485 c.912C>G p.I304M Substitution - Missense 19:10491990-10491990 - 215 COSM564847 c.1408C>T p.R470C Substitution - Missense 19:10489771-10489771 - SM-4AX85 COSM1726253 c.805C>T p.R269W Substitution - Missense 19:10492097-10492097 - SNU-C4 COSM4653016 c.847A>C p.M283L Substitution - Missense 19:10492055-10492055 - 112497 COSM94569 c.1687C>G p.Q563E Substitution - Missense 19:10489213-10489213 - TCGA-A6-5665-01 COSM1390139 c.24C>T p.S8S Substitution - coding silent 19:10500010-10500010 - SH-7032 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - YURIF COSM1711813 c.1376G>A p.R459Q Substitution - Missense 19:10489803-10489803 - 101189 COSM96325 c.652G>C p.E218Q Substitution - Missense 19:10492250-10492250 - RK022_C01 COSM1630692 c.483G>A p.M161I Substitution - Missense 19:10499551-10499551 - 587228 COSM564829 c.425C>T p.T142M Substitution - Missense 19:10499609-10499609 - SH-5693 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - GC_353T-GC_353N COSM4773549 c.1760A>G p.D587G Substitution - Missense 19:10486767-10486767 - TCGA-18-3407-01 COSM710187 c.463G>T p.V155F Substitution - Missense 19:10499571-10499571 - MO_1012 COSM5550782 c.284C>T p.A95V Substitution - Missense 19:10499750-10499750 - BN32T COSM1611495 c.187G>A p.A63T Substitution - Missense 19:10499847-10499847 - HCC39T COSM1611494 c.722G>A p.C241Y Substitution - Missense 19:10492180-10492180 - TCGA-A8-A09W-01 COSM438483 c.1356_1357insA p.V453fs*27 Insertion - Frameshift 19:10489822-10489823 - ccRCC-11 COSM710192 c.779G>A p.R260Q Substitution - Missense 19:10492123-10492123 - 2530678 COSM5885488 c.1284C>G p.V428V Substitution - coding silent 19:10491618-10491618 - NCI-H460 COSM1196953 c.706G>C p.D236H Substitution - Missense 19:10492196-10492196 - HCC2998 COSM1680643 c.793C>T p.Q265* Substitution - Nonsense 19:10492109-10492109 - LUAD-S01404 COSM398736 c.1165G>T p.D389Y Substitution - Missense 19:10491737-10491737 - I2L-P19Tb-Tumor-Organoid COSM5364723 c.1174delG p.A392fs*8 Deletion - Frameshift 19:10491728-10491728 - 180T COSM1726253 c.805C>T p.R269W Substitution - Missense 19:10492097-10492097 - S01524 COSM5669306 c.968delA p.K323fs*5 Deletion - Frameshift 19:10491934-10491934 - S04-32572-TP COSM4991203 c.1837T>C p.C613R Substitution - Missense 19:10486690-10486690 - KM12 COSM2812660 c.88G>A p.A30T Substitution - Missense 19:10499946-10499946 - TCGA-66-2773-01 COSM710195 c.959G>A p.R320Q Substitution - Missense 19:10491943-10491943 - TCGA-KK-A59V-01 COSM4878962 c.1753G>A p.D585N Substitution - Missense 19:10486774-10486774 - TCGA-66-2777-01 COSM710189 c.671C>A p.S224Y Substitution - Missense 19:10492231-10492231 - ESCC-210T COSM3937822 c.1454A>G p.N485S Substitution - Missense 19:10489725-10489725 - CHC1616T COSM4951265 c.212G>A p.R71Q Substitution - Missense 19:10499822-10499822 - TCGA-A4-A5XZ-01 COSM3989652 c.144C>A p.G48G Substitution - coding silent 19:10499890-10499890 - LUAD-S00488 COSM395069 c.1090G>T p.G364C Substitution - Missense 19:10491812-10491812 - SNU-175 COSM2812600 c.1519C>T p.R507* Substitution - Nonsense 19:10489660-10489660 - CSCC-29-T COSM4531303 c.1777G>A p.E593K Substitution - Missense 19:10486750-10486750 - DM28 COSM5611323 c.1048_1049GG>AA p.G350N Substitution - Missense 19:10491853-10491854 - TCGA-CM-6674-01 COSM1390137 c.493G>A p.D165N Substitution - Missense 19:10499541-10499541 - TCGA-66-2756-01 COSM710196 c.1105G>C p.V369L Substitution - Missense 19:10491797-10491797 - TCGA-A8-A09W-01 COSM438484 c.1353delC p.L452fs*6 Deletion - Frameshift 19:10489826-10489826 - CHC1152T COSM4949871 c.1326-2A>T p.? Unknown 19:10489855-10489855 - TCGA-CC-A7IK-01 COSM4924669 c.833C>T p.P278L Substitution - Missense 19:10492069-10492069 - NCI-H322M COSM1195038 c.1380G>T p.R460S Substitution - Missense 19:10489799-10489799 - sysucc-274T COSM5476019 c.143G>A p.G48D Substitution - Missense 19:10499891-10499891 - 202_T COSM3959484 c.932A>C p.H311P Substitution - Missense 19:10491970-10491970 - 112503 COSM94572 c.1085G>A p.R362Q Substitution - Missense 19:10491817-10491817 - RK259_C01 COSM4944610 c.798G>A p.A266A Substitution - coding silent 19:10492104-10492104 - ESOSCC160T COSM1172563 c.413A>C p.E138A Substitution - Missense 19:10499621-10499621 - TCGA-G2-A3IE-01 COSM1303939 c.730G>A p.E244K Substitution - Missense 19:10492172-10492172 - 9149_T COSM5042226 c.1744G>A p.E582K Substitution - Missense 19:10486783-10486783 - LUAD-RT-S01769 COSM392221 c.939delC p.T314fs*3 Deletion - Frameshift 19:10491963-10491963 - LUAD-RT-S01774 COSM381459 c.1532-2A>G p.? Unknown 19:10489370-10489370 - TCGA-DK-A1A3-01 COSM417774 c.73G>A p.E25K Substitution - Missense 19:10499961-10499961 - RKO COSM2812611 c.1048G>A p.G350S Substitution - Missense 19:10491854-10491854 - SNUH_G16_S1 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - Sample_1 COSM5021994 c.24C>G p.S8R Substitution - Missense 19:10500010-10500010 - 2011-2325:2012-337-T COSM96325 c.652G>C p.E218Q Substitution - Missense 19:10492250-10492250 - TCGA-BS-A0TE-01 COSM990602 c.1554_1555insT p.I519fs*8 Insertion - Frameshift 19:10489345-10489346 - 587226 COSM1211810 c.572C>A p.A191D Substitution - Missense 19:10499462-10499462 - TARGET-30-PASVRU COSM1285709 c.103_104TC>AT p.S35I Substitution - Missense 19:10499930-10499931 - LP6007546-DNA_A01 COSM5952474 c.43C>T p.R15* Substitution - Nonsense 19:10499991-10499991 - 93VU147T COSM4590889 c.457C>T p.L153F Substitution - Missense 19:10499577-10499577 - LC_S12 COSM1189873 c.1090G>A p.G364S Substitution - Missense 19:10491812-10491812 - J54_T COSM1524064 c.1409G>A p.R470H Substitution - Missense 19:10489770-10489770 - SH-9161 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - TCGA-BS-A0TA-01 COSM990606 c.505C>T p.R169C Substitution - Missense 19:10499529-10499529 - TCGA-24-2035-01 COSM80046 c.135C>A p.S45S Substitution - coding silent 19:10499899-10499899 - TCGA-EE-A2MS-06 COSM2812652 c.132C>T p.P44P Substitution - coding silent 19:10499902-10499902 - CHC1737T COSM4951275 c.1136G>A p.G379D Substitution - Missense 19:10491766-10491766 - TCGA-D1-A103-01 COSM990609 c.149G>A p.R50H Substitution - Missense 19:10499885-10499885 - 1953_T COSM3959486 c.466A>T p.M156L Substitution - Missense 19:10499568-10499568 - TCGA-B5-A0JY-01 COSM990603 c.1464G>T p.E488D Substitution - Missense 19:10489715-10489715 - TCGA-CG-5721-01 COSM4073864 c.1622C>T p.T541I Substitution - Missense 19:10489278-10489278 - TCGA-24-1474-01 COSM116773 c.567C>G p.N189K Substitution - Missense 19:10499467-10499467 - TCGA-P4-A5EB-01 COSM3989651 c.532C>T p.Q178* Substitution - Nonsense 19:10499502-10499502 - BD87T COSM3932863 c.1611C>T p.Y537Y Substitution - coding silent 19:10489289-10489289 - UM-SCC-2 COSM2812662 c.25G>A p.G9R Substitution - Missense 19:10500009-10500009 - 436 COSM4434025 c.557G>T p.G186V Substitution - Missense 19:10499477-10499477 - PCSI_0218_Pa_P_526 COSM3787539 c.120G>A p.A40A Substitution - coding silent 19:10499914-10499914 - TCGA-CG-4305-01 COSM4073866 c.932A>G p.H311R Substitution - Missense 19:10491970-10491970 - 112509 COSM94568 c.1715A>G p.Y572C Substitution - Missense 19:10486812-10486812 - PCSI_0083_Pa_P_526 COSM3787538 c.1083G>A p.P361P Substitution - coding silent 19:10491819-10491819 - SH-3776 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - A549 COSM1193323 c.997G>T p.G333C Substitution - Missense 19:10491905-10491905 - LUAD-RT-S01702 COSM379170 c.815G>A p.R272H Substitution - Missense 19:10492087-10492087 - TCGA-43-2578-01 COSM710188 c.499G>T p.V167F Substitution - Missense 19:10499535-10499535 - ccRCC-46 COSM1662410 c.1735G>T p.D579Y Substitution - Missense 19:10486792-10486792 - ESCC_162 COSM94572 c.1085G>A p.R362Q Substitution - Missense 19:10491817-10491817 - SH-3133 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - SH-1362 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - TCGA-EE-A2MR-06 COSM564847 c.1408C>T p.R470C Substitution - Missense 19:10489771-10489771 - 101286 COSM94570 c.1570G>T p.G524C Substitution - Missense 19:10489330-10489330 - TCGA-BR-8680-01 COSM990609 c.149G>A p.R50H Substitution - Missense 19:10499885-10499885 - 304_T COSM710198 c.1264G>A p.D422N Substitution - Missense 19:10491638-10491638 - 112313 COSM94573 c.1000T>C p.Y334H Substitution - Missense 19:10491902-10491902 - TCGA-DD-A1EL-01 COSM4925833 c.811G>T p.V271L Substitution - Missense 19:10492091-10492091 - TCGA-EI-6882-01 COSM3422378 c.1392C>T p.G464G Substitution - coding silent 19:10489787-10489787 - CSCC-38-T COSM4450725 c.805delC p.R269fs*8 Deletion - Frameshift 19:10492097-10492097 - SM-4B296 COSM4410364 c.10G>C p.D4H Substitution - Missense 19:10500024-10500024 - sysucc-1163T COSM5458701 c.640-4G>A p.? Unknown 19:10492266-10492266 - 86835 COSM96324 c.778C>T p.R260* Substitution - Nonsense 19:10492124-10492124 - LUAD-B02477 COSM335836 c.779G>T p.R260L Substitution - Missense 19:10492123-10492123 - TCGA-G2-A2EJ-01 COSM1303938 c.948G>A p.V316V Substitution - coding silent 19:10491954-10491954 - HCC066T COSM5821024 c.721T>C p.C241R Substitution - Missense 19:10492181-10492181 - TCGA-EE-A2GC-06 COSM3528284 c.1479G>A p.E493E Substitution - coding silent 19:10489700-10489700 - CHC798T COSM5348788 c.1187_1188insC p.N397fs*18 Insertion - Frameshift 19:10491714-10491715 - TCGA-BR-4184-01 COSM4073874 c.100G>A p.A34T Substitution - Missense 19:10499934-10499934 - HCC5T COSM3718029 c.1751A>G p.Y584C Substitution - Missense 19:10486776-10486776 - 360_T COSM564847 c.1408C>T p.R470C Substitution - Missense 19:10489771-10489771 - SH-0348 COSM4606146 c.93G>A p.V31V Substitution - coding silent 19:10499941-10499941 - LUAD-S01409 COSM346494 c.959G>C p.R320P Substitution - Missense 19:10491943-10491943 - TCGA-K7-A5RG-01 COSM4930153 c.1136G>T p.G379V Substitution - Missense 19:10491766-10491766 - ESCC-212T COSM3937823 c.709C>A p.L237M Substitution - Missense 19:10492193-10492193 - 4537_T COSM1524056 c.653A>T p.E218V Substitution - Missense 19:10492249-10492249 - CHC2128T COSM2812613 c.990C>T p.T330T Substitution - coding silent 19:10491912-10491912 - TCGA-BR-7707-01 COSM4073872 c.234C>T p.D78D Substitution - coding silent 19:10499800-10499800 - DM14 COSM5609242 c.1413C>T p.L471L Substitution - coding silent 19:10489766-10489766 - S02120 COSM2812655 c.119C>T p.A40V Substitution - Missense 19:10499915-10499915 - H460 COSM1196953 c.706G>C p.D236H Substitution - Missense 19:10492196-10492196 - TCGA-GC-A3WC-01 COSM3796565 c.347G>C p.R116P Substitution - Missense 19:10499687-10499687 - SH-2871 COSM148507 c.1413C>G p.L471L Substitution - coding silent 19:10489766-10489766 - HCC5 COSM3718029 c.1751A>G p.Y584C Substitution - Missense 19:10486776-10486776 - RK284_C01 COSM1524064 c.1409G>A p.R470H Substitution - Missense 19:10489770-10489770 - LUAD-RT-S01487 COSM377897 c.833C>G p.P278R Substitution - Missense 19:10492069-10492069 - CN-AML-CR-24-Dx COSM3932863 c.1611C>T p.Y537Y Substitution - coding silent 19:10489289-10489289 - 15145 COSM564847 c.1408C>T p.R470C Substitution - Missense 19:10489771-10489771 - HCC174 COSM3718030 c.742G>A p.A248T Substitution - Missense 19:10492160-10492160 - TCGA-BR-8372-01 COSM4073865 c.1609T>C p.Y537H Substitution - Missense 19:10489291-10489291 - TCGA-HJ-7597-01 COSM2812641 c.444C>T p.G148G Substitution - coding silent 19:10499590-10499590 - TCGA-BP-5183-01 COSM474128 c.1226T>C p.M409T Substitution - Missense 19:10491676-10491676 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.465870 19p13.2 606016 2420339|CGAP|BC002417|C/G|coding|Leu471Leu|1442|Validated; 2420339|CGAP|BC002930|C/G|coding|Leu471Leu|1518|Validated; 2420339|CGAP|BC015945|C/G|coding|Leu471Leu|1453|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - A Frameshift p.I519Yfs*8 c.1554dupT 19 10600022 UCEC A G Missense p.I185T c.554T>C 19 10610156 UCEC A G Missense p.L268P c.803T>C 19 10602775 LUAD A G Missense p.L310P c.929T>C 19 10602649 LUSC A G Missense p.M409T c.1226T>C 19 10602352 RCCC A G Missense p.V155A c.464T>C 19 10610246 LUAD A G Missense p.W544R c.1630T>C 19 10599946 RCCC A G Synonymous p.P105P c.315T>C 19 10610395 RCCC A T Missense p.M503K c.1508T>A 19 10600347 LUAD - CA Frameshift p.R536Lfs*13 c.1606_1607insTG 19 10599969 BLCA C A Missense p.C319F c.956G>T 19 10602622 HNSC C A Missense p.G332C c.994G>T 19 10602584 LUAD C A Missense p.G332C c.994G>T 19 10602584 NSCLC C A Missense p.G423V c.1268G>T 19 10602310 LUAD C A Missense p.G423V c.1268G>T 19 10602310 LUSC C A Missense p.G480W c.1438G>T 19 10600417 LUSC C A Missense p.G509W c.1525G>T 19 10600330 LUAD C A Missense p.G524C c.1570G>T 19 10600006 LUAD C A Missense p.G603W c.1807G>T 19 10597396 LUAD C A Missense p.Q163H c.489G>T 19 10610221 LUAD C A Missense p.R15L c.44G>T 19 10610666 LUSC C A Missense p.R260L c.779G>T 19 10602799 LUAD C A Missense p.R354L c.1061G>T 19 10602517 PRAD C A Missense p.V123L c.367G>T 19 10610343 LUAD C A Missense p.V155F c.463G>T 19 10610247 LUSC C A Missense p.V167F c.499G>T 19 10610211 LUSC C A Missense p.V214L c.640G>T 19 10602938 LUAD C A Missense p.V418L c.1252G>T 19 10602326 LUSC C A Missense p.V99L c.295G>T 19 10610415 LUAD C A Missense p.W544C c.1632G>T 19 10599944 LUSC C A Nonsense p.E449* c.1345G>T 19 10600510 LUAD C A Synonymous p.A331A c.993G>T 19 10602585 NSCLC CC AA Missense p.G527F c.1579_1580delinsTT 19 10599996 LUAD C - Frameshift p.E593Rfs*2 c.1777delG 19 10597426 LUAD - C Frameshift p.V302Gfs*48 c.904dupG 19 10602674 CM C G Missense p.A607P c.1819G>C 19 10597384 HNSC C G Missense p.E218Q c.652G>C 19 10602926 BLCA C G Missense p.E493D c.1479G>C 19 10600376 LUSC C G Missense p.R204P c.611G>C 19 10610099 LUAD C G Missense p.R261P c.782G>C 19 10602796 LUAD C G Missense p.V369L c.1105G>C 19 10602473 LUSC C T Missense p.A522V c.1565C>T 19 10600011 BRCA C T Missense p.C23Y c.68G>A 19 10610642 HNSC C T Missense p.D422N c.1264G>A 19 10602314 LUSC C T Missense p.E244K c.730G>A 19 10602848 BLCA C T Missense p.E25K c.73G>A 19 10610637 BLCA C T Missense p.G333S c.997G>A 19 10602581 LUAD C T Missense p.G417E c.1250G>A 19 10602328 LUAD C T Missense p.G417R c.1249G>A 19 10602329 LUAD C T Missense p.G477S c.1429G>A 19 10600426 THCA C T Missense p.M161I c.483G>A 19 10610227 HC C T Missense p.R260Q c.779G>A 19 10602799 LUSC C T Missense p.R320Q c.959G>A 19 10602619 LUSC C T Missense p.R415H c.1244G>A 19 10602334 LUAD C T Missense p.R470H c.1409G>A 19 10600446 HNSC C T Missense p.V324M c.970G>A 19 10602608 ESCA C T Missense p.V369M c.1105G>A 19 10602473 HNSC C T Synonymous p.E493E c.1479G>A 19 10600376 CM C T Synonymous p.G564G c.1692G>A 19 10599884 CM C T Synonymous p.Q282Q c.846G>A 19 10602732 HNSC C T Synonymous p.V316V c.948G>A 19 10602630 BLCA C T Synonymous p.V428V c.1284C>T 19 10602294 PAAD GA AT Missense p.S35I c.103_104delinsAT 19 10610606 NB G A Missense p.A407V c.1220C>T 19 10602358 PRAD G A Missense p.C23Y c.68G>A 19 10610642 BRCA G A Missense p.P130L c.389C>T 19 10610321 CM G A Missense p.R169C c.505C>T 19 10610205 HNSC G A Missense p.R169C c.505C>T 19 10610205 UCEC G A Missense p.R272C c.814C>T 19 10602764 HNSC G A Missense p.R415C c.1243C>T 19 10602335 LUAD G A Missense p.R470C c.1408C>T 19 10600447 HNSC G A Missense p.R470C c.1408C>T 19 10600447 LUAD G A Missense p.R470C c.1408C>T 19 10600447 LUSC G A Missense p.R470C c.1408C>T 19 10600447 NSCLC G A Missense p.R483C c.1447C>T 19 10600408 LUAD G A Missense p.S144F c.431C>T 19 10610279 LUAD G A Missense p.T142M c.425C>T 19 10610285 LUAD G A Nonsense p.Q46* c.136C>T 19 10610574 LUAD G A Nonsense p.Q75* c.223C>T 19 10610487 LUSC G A Synonymous p.I164I c.492C>T 19 10610218 UCEC G A Synonymous p.I187I c.561C>T 19 10610149 HNSC G A Synonymous p.N279N c.837C>T 19 10602741 CM G A Synonymous p.P44P c.132C>T 19 10610578 CM G A Synonymous p.Y206Y c.618C>T 19 10610092 STAD G C Missense p.F246L c.738C>G 19 10602840 LUAD G C Missense p.H96Q c.288C>G 19 10610422 NSCLC G C Missense p.L231V c.691C>G 19 10602887 LUSC G C Missense p.N189K c.567C>G 19 10610143 OV G C Missense p.S243C c.728C>G 19 10602850 LUSC G - Frameshift p.L452Wfs*6 c.1353delC 19 10600502 BRCA G T Missense p.F139L c.417C>A 19 10610293 LUAD G T Missense p.R470S c.1408C>A 19 10600447 LUAD G T Missense p.S224Y c.671C>A 19 10602907 LUSC G T Missense p.S45Y c.134C>A 19 10610576 HNSC G T Synonymous p.A95A c.285C>A 19 10610425 STAD G T Synonymous p.S45S c.135C>A 19 10610575 OV T A Missense p.I145F c.433A>T 19 10610277 HNSC T A Missense p.I145F c.433A>T 19 10610277 LUAD T A Missense p.I328F c.982A>T 19 10602596 LUAD T A Missense p.Q178L c.533A>T 19 10610177 HNSC T A Missense p.Q284L c.851A>T 19 10602727 LUAD T A Nonsense p.K287* c.859A>T 19 10602719 LUAD T C Missense p.D479G c.1436A>G 19 10600419 LUAD T C Missense p.H311R c.932A>G 19 10602646 STAD T C Missense p.I506V c.1516A>G 19 10600339 LUSC T C Missense p.M110V c.328A>G 19 10610382 LUAD T C Missense p.M156V c.466A>G 19 10610244 LUAD T C Missense p.R460G c.1378A>G 19 10600477 LUAD T C Missense p.T598A c.1792A>G 19 10597411 HNSC - T Frameshift p.N469Kfs*11 c.1406dupA 19 10600449 LUSC - T Frameshift p.V453Gfs*27 c.1355_1356insA 19 10600499 BRCA