Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 11 55652912 55652912 + Missense_Mutation SNP C C G TCGA-FD-A6TH-01A-11D-A32B-08 TCGA-FD-A6TH-10A-01D-A329-08 g.chr11:55652912C>G c.8C>G c.(7-9)tCt>tGt p.S3C BLCA 11 55653114 55653114 + Silent SNP G G A TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr11:55653114G>A c.210G>A c.(208-210)ttG>ttA p.L70L BLCA 11 55653304 55653304 + Nonsense_Mutation SNP G G T TCGA-GC-A3WC-01A-31D-A22Z-08 TCGA-GC-A3WC-10A-01D-A22Z-08 g.chr11:55653304G>T c.400G>T c.(400-402)Gag>Tag p.E134* BLCA 11 55655616 55655616 + Missense_Mutation SNP G G A TCGA-DK-A3X2-01A-11D-A22Z-08 TCGA-DK-A3X2-10A-01D-A22Z-08 g.chr11:55655616G>A c.616G>A c.(616-618)Gag>Aag p.E206K BLCA 11 55655653 55655653 + Missense_Mutation SNP G G C TCGA-GU-A764-01A-11D-A34U-08 TCGA-GU-A764-10B-01D-A34X-08 g.chr11:55655653G>C c.653G>C c.(652-654)aGa>aCa p.R218T BLCA 11 55655686 55655686 + Missense_Mutation SNP T T C TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chr11:55655686T>C c.686T>C c.(685-687)aTg>aCg p.M229T BLCA 11 55657471 55657471 + Missense_Mutation SNP C C A TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr11:55657471C>A c.815C>A c.(814-816)gCa>gAa p.A272E BLCA 11 55658689 55658689 + Missense_Mutation SNP G G C TCGA-G2-A2EF-01A-12D-A18F-08 TCGA-G2-A2EF-10A-01D-A18F-08 g.chr11:55658689G>C c.940G>C c.(940-942)Gac>Cac p.D314H BLCA 11 55658697 55658697 + Silent SNP A A G TCGA-DK-AA76-01A-11D-A391-08 TCGA-DK-AA76-10A-01D-A394-08 g.chr11:55658697A>G c.948A>G c.(946-948)caA>caG p.Q316Q BLCA 11 55658785 55658785 + Missense_Mutation SNP C C T TCGA-GD-A3OQ-01A-32D-A21Z-08 TCGA-GD-A3OQ-10A-01D-A21Z-08 g.chr11:55658785C>T c.1036C>T c.(1036-1038)Cat>Tat p.H346Y BRCA 11 55653691 55653691 + Nonsense_Mutation SNP G G A TCGA-BH-A0HP-01A-12D-A099-09 TCGA-BH-A0HP-10A-01D-A099-09 g.chr11:55653691G>A c.504G>A c.(502-504)tgG>tgA p.W168* BRCA 11 55657466 55657466 + Silent SNP C C T TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr11:55657466C>T c.810C>T c.(808-810)ctC>ctT p.L270L BRCA 11 55658869 55658869 + Missense_Mutation SNP G G A TCGA-A8-A09Q-01A-11W-A019-09 TCGA-A8-A09Q-10A-01W-A021-09 g.chr11:55658869G>A c.1120G>A c.(1120-1122)Gag>Aag p.E374K CESC 11 55653082 55653082 + Missense_Mutation SNP C C T TCGA-HM-A3JK-01A-11D-A21Q-09 TCGA-HM-A3JK-10A-01D-A21Q-09 g.chr11:55653082C>T c.178C>T c.(178-180)Cgg>Tgg p.R60W CESC 11 55653304 55653304 + Missense_Mutation SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr11:55653304G>A c.400G>A c.(400-402)Gag>Aag p.E134K CESC 11 55658629 55658629 + Missense_Mutation SNP G G A TCGA-EK-A2PM-01A-11D-A18J-09 TCGA-EK-A2PM-10A-01D-A18J-09 g.chr11:55658629G>A c.880G>A c.(880-882)Gaa>Aaa p.E294K COAD 11 55653041 55653041 + Missense_Mutation SNP C C T TCGA-CM-6679-01A-11D-1835-10 TCGA-CM-6679-10A-01D-1835-10 g.chr11:55653041C>T c.137C>T c.(136-138)aCg>aTg p.T46M COAD 11 55653082 55653082 + Missense_Mutation SNP C C T TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr11:55653082C>T c.178C>T c.(178-180)Cgg>Tgg p.R60W COAD 11 55653129 55653129 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr11:55653129C>T c.225C>T c.(223-225)ttC>ttT p.F75F COAD 11 55655586 55655586 + Missense_Mutation SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr11:55655586C>T c.586C>T c.(586-588)Cat>Tat p.H196Y COAD 11 55655610 55655610 + Missense_Mutation SNP G G A TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr11:55655610G>A c.610G>A c.(610-612)Gag>Aag p.E204K COAD 11 55655682 55655682 + Nonsense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:55655682G>T c.682G>T c.(682-684)Gga>Tga p.G228* COAD 11 55655690 55655690 + Nonsense_Mutation SNP T T G TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr11:55655690T>G c.690T>G c.(688-690)taT>taG p.Y230* COAD 11 55657418 55657418 + Splice_Site SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:55657418G>A c.762G>A c.(760-762)agG>agA p.R254R COAD 11 55657450 55657450 + Missense_Mutation SNP C C A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr11:55657450C>A c.794C>A c.(793-795)cCt>cAt p.P265H COAD 11 55658833 55658833 + Missense_Mutation SNP T T C TCGA-AA-3819-01A-01W-0900-09 TCGA-AA-3819-10A-01W-0900-09 g.chr11:55658833T>C c.1084T>C c.(1084-1086)Tgg>Cgg p.W362R COAD 11 55659006 55659006 + Silent SNP C C A TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr11:55659006C>A c.1257C>A c.(1255-1257)acC>acA p.T419T COAD 11 55659028 55659028 + Missense_Mutation SNP C C A TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr11:55659028C>A c.1279C>A c.(1279-1281)Caa>Aaa p.Q427K COAD 11 55659031 55659031 + Missense_Mutation SNP A A C TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr11:55659031A>C c.1282A>C c.(1282-1284)Agt>Cgt p.S428R COADREAD 11 55653041 55653041 + Missense_Mutation SNP C C T TCGA-CM-6679-01A-11D-1835-10 TCGA-CM-6679-10A-01D-1835-10 g.chr11:55653041C>T c.137C>T c.(136-138)aCg>aTg p.T46M COADREAD 11 55653082 55653082 + Missense_Mutation SNP C C T TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr11:55653082C>T c.178C>T c.(178-180)Cgg>Tgg p.R60W COADREAD 11 55653129 55653129 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr11:55653129C>T c.225C>T c.(223-225)ttC>ttT p.F75F COADREAD 11 55655586 55655586 + Missense_Mutation SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr11:55655586C>T c.586C>T c.(586-588)Cat>Tat p.H196Y COADREAD 11 55655610 55655610 + Missense_Mutation SNP G G A TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr11:55655610G>A c.610G>A c.(610-612)Gag>Aag p.E204K COADREAD 11 55655682 55655682 + Nonsense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:55655682G>T c.682G>T c.(682-684)Gga>Tga p.G228* COADREAD 11 55655690 55655690 + Nonsense_Mutation SNP T T G TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr11:55655690T>G c.690T>G c.(688-690)taT>taG p.Y230* COADREAD 11 55657418 55657418 + Splice_Site SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:55657418G>A c.762G>A c.(760-762)agG>agA p.R254R COADREAD 11 55657450 55657450 + Missense_Mutation SNP C C A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr11:55657450C>A c.794C>A c.(793-795)cCt>cAt p.P265H COADREAD 11 55658833 55658833 + Missense_Mutation SNP T T C TCGA-AA-3819-01A-01W-0900-09 TCGA-AA-3819-10A-01W-0900-09 g.chr11:55658833T>C c.1084T>C c.(1084-1086)Tgg>Cgg p.W362R COADREAD 11 55658984 55658984 + Missense_Mutation SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:55658984T>C c.1235T>C c.(1234-1236)tTc>tCc p.F412S COADREAD 11 55659006 55659006 + Silent SNP C C A TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr11:55659006C>A c.1257C>A c.(1255-1257)acC>acA p.T419T COADREAD 11 55659028 55659028 + Missense_Mutation SNP C C A TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr11:55659028C>A c.1279C>A c.(1279-1281)Caa>Aaa p.Q427K COADREAD 11 55659031 55659031 + Missense_Mutation SNP A A C TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr11:55659031A>C c.1282A>C c.(1282-1284)Agt>Cgt p.S428R ESCA 11 55653117 55653117 + Silent SNP G G A TCGA-L5-A4OE-01A-11D-A27G-09 TCGA-L5-A4OE-11A-11D-A27G-09 g.chr11:55653117G>A c.213G>A c.(211-213)aaG>aaA p.K71K ESCA 11 55657514 55657514 + Splice_Site SNP A A T TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr11:55657514A>T c.858A>T c.(856-858)agA>agT p.R286S GBM 11 55653041 55653041 + Missense_Mutation SNP C C T TCGA-06-0879-01A-01W-0424-08 TCGA-06-0879-10A-01W-0424-08 g.chr11:55653041C>T c.137C>T c.(136-138)aCg>aTg p.T46M GBM 11 55653196 55653197 + Missense_Mutation DNP GA GA TC TCGA-06-0168-01A-01D-1491-08 TCGA-06-0168-10A-01D-1491-08 g.chr11:55653196_55653197GA>TC c.292_293GA>TC c.(292-294)GAg>TCg p.E98S GBM 11 55653246 55653246 + Silent SNP G G A TCGA-06-0119-01A-08D-1490-08 TCGA-06-0119-10A-01D-1490-08 g.chr11:55653246G>A c.342G>A c.(340-342)ccG>ccA p.P114P GBM 11 55653609 55653610 + Frame_Shift_Ins INS - - A TCGA-12-0618-01A-01D-1492-08 TCGA-12-0618-10A-01D-1492-08 g.chr11:55653609_55653610insA c.422_423insA c.(421-426)ctaaaafs p.LK141fs GBM 11 55655555 55655555 + Missense_Mutation SNP G G T TCGA-76-4928-01B-01D-1486-08 TCGA-76-4928-10A-01D-1486-08 g.chr11:55655555G>T c.555G>T c.(553-555)aaG>aaT p.K185N GBM 11 55655591 55655591 + Missense_Mutation SNP C C A TCGA-16-0846-01A-01W-0424-08 TCGA-16-0846-10A-01W-0424-08 g.chr11:55655591C>A c.591C>A c.(589-591)caC>caA p.H197Q GBM 11 55658647 55658647 + Missense_Mutation SNP A A T TCGA-06-0168-01A-01D-1491-08 TCGA-06-0168-10A-01D-1491-08 g.chr11:55658647A>T c.898A>T c.(898-900)Atc>Ttc p.I300F GBM 11 55658914 55658914 + Missense_Mutation SNP T T A TCGA-06-0168-01A-01D-1491-08 TCGA-06-0168-10A-01D-1491-08 g.chr11:55658914T>A c.1165T>A c.(1165-1167)Tgc>Agc p.C389S GBMLGG 11 55653034 55653034 + Nonsense_Mutation SNP C C T TCGA-DU-6402-01A-11D-1705-08 TCGA-DU-6402-10A-01D-1705-08 g.chr11:55653034C>T c.130C>T c.(130-132)Caa>Taa p.Q44* GBMLGG 11 55653041 55653041 + Missense_Mutation SNP C C T TCGA-06-0879-01A-01W-0424-08 TCGA-06-0879-10A-01W-0424-08 g.chr11:55653041C>T c.137C>T c.(136-138)aCg>aTg p.T46M GBMLGG 11 55653196 55653197 + Missense_Mutation DNP GA GA TC TCGA-06-0168-01A-01D-1491-08 TCGA-06-0168-10A-01D-1491-08 g.chr11:55653196_55653197GA>TC c.292_293GA>TC c.(292-294)GAg>TCg p.E98S GBMLGG 11 55653246 55653246 + Silent SNP G G A TCGA-06-0119-01A-08D-1490-08 TCGA-06-0119-10A-01D-1490-08 g.chr11:55653246G>A c.342G>A c.(340-342)ccG>ccA p.P114P GBMLGG 11 55653246 55653246 + Silent SNP G G A TCGA-HT-A4DS-01A-11D-A26M-08 TCGA-HT-A4DS-10A-01D-A26K-08 g.chr11:55653246G>A c.342G>A c.(340-342)ccG>ccA p.P114P GBMLGG 11 55653609 55653610 + Frame_Shift_Ins INS - - A TCGA-12-0618-01A-01D-1492-08 TCGA-12-0618-10A-01D-1492-08 g.chr11:55653609_55653610insA c.422_423insA c.(421-426)ctaaaafs p.LK141fs GBMLGG 11 55655555 55655555 + Missense_Mutation SNP G G T TCGA-76-4928-01B-01D-1486-08 TCGA-76-4928-10A-01D-1486-08 g.chr11:55655555G>T c.555G>T c.(553-555)aaG>aaT p.K185N GBMLGG 11 55655591 55655591 + Missense_Mutation SNP C C A TCGA-16-0846-01A-01W-0424-08 TCGA-16-0846-10A-01W-0424-08 g.chr11:55655591C>A c.591C>A c.(589-591)caC>caA p.H197Q GBMLGG 11 55655604 55655604 + Nonsense_Mutation SNP C C T TCGA-DU-5872-01A-11D-1705-08 TCGA-DU-5872-10A-01D-1705-08 g.chr11:55655604C>T c.604C>T c.(604-606)Cga>Tga p.R202* GBMLGG 11 55658647 55658647 + Missense_Mutation SNP A A T TCGA-06-0168-01A-01D-1491-08 TCGA-06-0168-10A-01D-1491-08 g.chr11:55658647A>T c.898A>T c.(898-900)Atc>Ttc p.I300F GBMLGG 11 55658726 55658726 + Missense_Mutation SNP A A T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:55658726A>T c.977A>T c.(976-978)gAa>gTa p.E326V GBMLGG 11 55658914 55658914 + Missense_Mutation SNP T T A TCGA-06-0168-01A-01D-1491-08 TCGA-06-0168-10A-01D-1491-08 g.chr11:55658914T>A c.1165T>A c.(1165-1167)Tgc>Agc p.C389S GBMLGG 11 55658975 55658975 + Missense_Mutation SNP T T C TCGA-WY-A85D-01A-11D-A36O-08 TCGA-WY-A85D-10A-01D-A367-08 g.chr11:55658975T>C c.1226T>C c.(1225-1227)gTa>gCa p.V409A GBMLGG 11 55659044 55659044 + Missense_Mutation SNP A A T TCGA-DB-5277-01A-01D-1468-08 TCGA-DB-5277-10A-01D-1468-08 g.chr11:55659044A>T c.1295A>T c.(1294-1296)tAc>tTc p.Y432F HNSC 11 55652952 55652952 + Silent SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr11:55652952C>T c.48C>T c.(46-48)ccC>ccT p.P16P HNSC 11 55653067 55653067 + Missense_Mutation SNP T T G TCGA-CV-7263-01A-11D-2012-08 TCGA-CV-7263-10A-01D-2013-08 g.chr11:55653067T>G c.163T>G c.(163-165)Tgc>Ggc p.C55G HNSC 11 55653074 55653074 + Missense_Mutation SNP A A C TCGA-CR-7368-01A-11D-2129-08 TCGA-CR-7368-10A-01D-2129-08 g.chr11:55653074A>C c.170A>C c.(169-171)aAg>aCg p.K57T HNSC 11 55653083 55653083 + Missense_Mutation SNP G G A TCGA-P3-A6T2-01A-11D-A34J-08 TCGA-P3-A6T2-10A-01D-A34M-08 g.chr11:55653083G>A c.179G>A c.(178-180)cGg>cAg p.R60Q HNSC 11 55653117 55653117 + Missense_Mutation SNP G G T TCGA-P3-A6T0-01A-12D-A34J-08 TCGA-P3-A6T0-10A-01D-A34M-08 g.chr11:55653117G>T c.213G>T c.(211-213)aaG>aaT p.K71N HNSC 11 55653123 55653123 + Missense_Mutation SNP G G A TCGA-CV-7235-01A-11D-2012-08 TCGA-CV-7235-10A-01D-2013-08 g.chr11:55653123G>A c.219G>A c.(217-219)atG>atA p.M73I HNSC 11 55653151 55653151 + Missense_Mutation SNP C C T TCGA-CV-7097-01A-11D-2012-08 TCGA-CV-7097-10A-01D-2013-08 g.chr11:55653151C>T c.247C>T c.(247-249)Cgg>Tgg p.R83W HNSC 11 55653180 55653180 + Silent SNP A A T TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chr11:55653180A>T c.276A>T c.(274-276)atA>atT p.I92I HNSC 11 55653181 55653181 + Missense_Mutation SNP T T C TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr11:55653181T>C c.277T>C c.(277-279)Tgt>Cgt p.C93R HNSC 11 55653184 55653184 + Missense_Mutation SNP G G A TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr11:55653184G>A c.280G>A c.(280-282)Ggg>Agg p.G94R HNSC 11 55653198 55653198 + Missense_Mutation SNP G G C TCGA-DQ-5624-01A-01D-1870-08 TCGA-DQ-5624-10A-01D-1870-08 g.chr11:55653198G>C c.294G>C c.(292-294)gaG>gaC p.E98D HNSC 11 55653267 55653267 + Missense_Mutation SNP C C G TCGA-D6-6826-01A-11D-1912-08 TCGA-D6-6826-10A-01D-1912-08 g.chr11:55653267C>G c.363C>G c.(361-363)caC>caG p.H121Q HNSC 11 55653619 55653619 + Missense_Mutation SNP G G C TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr11:55653619G>C c.432G>C c.(430-432)atG>atC p.M144I HNSC 11 55653650 55653650 + Missense_Mutation SNP C C G TCGA-D6-A6ES-01A-12D-A31L-08 TCGA-D6-A6ES-10A-01D-A31J-08 g.chr11:55653650C>G c.463C>G c.(463-465)Ctc>Gtc p.L155V HNSC 11 55658863 55658863 + Missense_Mutation SNP G G C TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr11:55658863G>C c.1114G>C c.(1114-1116)Gat>Cat p.D372H HNSC 11 55658878 55658878 + Missense_Mutation SNP C C A TCGA-CR-6477-01A-11D-1870-08 TCGA-CR-6477-10A-01D-1870-08 g.chr11:55658878C>A c.1129C>A c.(1129-1131)Ctc>Atc p.L377I HNSC 11 55658917 55658917 + Missense_Mutation SNP A A C TCGA-CV-A45Z-01A-21D-A25D-08 TCGA-CV-A45Z-10A-01D-A25E-08 g.chr11:55658917A>C c.1168A>C c.(1168-1170)Agt>Cgt p.S390R HNSC 11 55658941 55658943 + In_Frame_Del DEL GTG GTG - TCGA-CV-6950-01A-11D-1912-08 TCGA-CV-6950-10A-01D-1912-08 g.chr11:55658941_55658943delGTG c.1192_1194delGTG c.(1192-1194)gtgdel p.V399del HNSC 11 55658943 55658943 + Silent SNP G G T TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chr11:55658943G>T c.1194G>T c.(1192-1194)gtG>gtT p.V398V HNSC 11 55658953 55658953 + Missense_Mutation SNP G G T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr11:55658953G>T c.1204G>T c.(1204-1206)Gtt>Ttt p.V402F HNSC 11 55658999 55658999 + Missense_Mutation SNP G G T TCGA-BA-A4IH-01A-11D-A25Y-08 TCGA-BA-A4IH-10A-01D-A25Y-08 g.chr11:55658999G>T c.1250G>T c.(1249-1251)gGt>gTt p.G417V HNSC 11 55659078 55659078 + Silent SNP C C T TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr11:55659078C>T c.1329C>T c.(1327-1329)ctC>ctT p.L443L KIPAN 11 55653066 55653066 + Missense_Mutation SNP A A T TCGA-B0-5088-01A-01D-1462-08 TCGA-B0-5088-11A-01D-1462-08 g.chr11:55653066A>T c.162A>T c.(160-162)gaA>gaT p.E54D KIPAN 11 55653105 55653105 + Missense_Mutation SNP C C A TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr11:55653105C>A c.201C>A c.(199-201)gaC>gaA p.D67E KIPAN 11 55653110 55653110 + Missense_Mutation SNP G G A TCGA-CZ-5985-01A-11D-1669-08 TCGA-CZ-5985-11A-01D-1669-08 g.chr11:55653110G>A c.206G>A c.(205-207)tGt>tAt p.C69Y KIPAN 11 55653128 55653128 + Missense_Mutation SNP T T A TCGA-B0-5075-01A-01D-1462-08 TCGA-B0-5075-11A-01D-1462-08 g.chr11:55653128T>A c.224T>A c.(223-225)tTc>tAc p.F75Y KIPAN 11 55658689 55658689 + Missense_Mutation SNP G G T TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr11:55658689G>T c.940G>T c.(940-942)Gac>Tac p.D314Y KIPAN 11 55658774 55658774 + Missense_Mutation SNP A A G TCGA-DW-7839-01A-11D-2136-08 TCGA-DW-7839-10A-01D-2136-08 g.chr11:55658774A>G c.1025A>G c.(1024-1026)tAt>tGt p.Y342C KIRC 11 55653066 55653066 + Missense_Mutation SNP A A T TCGA-B0-5088-01A-01D-1462-08 TCGA-B0-5088-11A-01D-1462-08 g.chr11:55653066A>T c.162A>T c.(160-162)gaA>gaT p.E54D KIRC 11 55653105 55653105 + Missense_Mutation SNP C C A TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr11:55653105C>A c.201C>A c.(199-201)gaC>gaA p.D67E KIRC 11 55653110 55653110 + Missense_Mutation SNP G G A TCGA-CZ-5985-01A-11D-1669-08 TCGA-CZ-5985-11A-01D-1669-08 g.chr11:55653110G>A c.206G>A c.(205-207)tGt>tAt p.C69Y KIRC 11 55653128 55653128 + Missense_Mutation SNP T T A TCGA-B0-5075-01A-01D-1462-08 TCGA-B0-5075-11A-01D-1462-08 g.chr11:55653128T>A c.224T>A c.(223-225)tTc>tAc p.F75Y KIRC 11 55658689 55658689 + Missense_Mutation SNP G G T TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr11:55658689G>T c.940G>T c.(940-942)Gac>Tac p.D314Y KIRP 11 55658774 55658774 + Missense_Mutation SNP A A G TCGA-DW-7839-01A-11D-2136-08 TCGA-DW-7839-10A-01D-2136-08 g.chr11:55658774A>G c.1025A>G c.(1024-1026)tAt>tGt p.Y342C LGG 11 55653034 55653034 + Nonsense_Mutation SNP C C T TCGA-DU-6402-01A-11D-1705-08 TCGA-DU-6402-10A-01D-1705-08 g.chr11:55653034C>T c.130C>T c.(130-132)Caa>Taa p.Q44* LGG 11 55653246 55653246 + Silent SNP G G A TCGA-HT-A4DS-01A-11D-A26M-08 TCGA-HT-A4DS-10A-01D-A26K-08 g.chr11:55653246G>A c.342G>A c.(340-342)ccG>ccA p.P114P LGG 11 55655604 55655604 + Nonsense_Mutation SNP C C T TCGA-DU-5872-01A-11D-1705-08 TCGA-DU-5872-10A-01D-1705-08 g.chr11:55655604C>T c.604C>T c.(604-606)Cga>Tga p.R202* LGG 11 55658726 55658726 + Missense_Mutation SNP A A T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:55658726A>T c.977A>T c.(976-978)gAa>gTa p.E326V LGG 11 55658975 55658975 + Missense_Mutation SNP T T C TCGA-WY-A85D-01A-11D-A36O-08 TCGA-WY-A85D-10A-01D-A367-08 g.chr11:55658975T>C c.1226T>C c.(1225-1227)gTa>gCa p.V409A LGG 11 55659044 55659044 + Missense_Mutation SNP A A T TCGA-DB-5277-01A-01D-1468-08 TCGA-DB-5277-10A-01D-1468-08 g.chr11:55659044A>T c.1295A>T c.(1294-1296)tAc>tTc p.Y432F LIHC 11 55653151 55653151 + Missense_Mutation SNP C C T TCGA-DD-AADE-01A-11D-A40R-10 TCGA-DD-AADE-10A-01D-A40U-10 g.chr11:55653151C>T c.247C>T c.(247-249)Cgg>Tgg p.R83W LIHC 11 55653258 55653258 + Silent SNP T T C TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr11:55653258T>C c.354T>C c.(352-354)tcT>tcC p.S118S LIHC 11 55655563 55655563 + Missense_Mutation SNP C C A TCGA-CC-A8HT-01A-11D-A35Z-10 TCGA-CC-A8HT-10A-01D-A35Z-10 g.chr11:55655563C>A c.563C>A c.(562-564)gCa>gAa p.A188E LIHC 11 55659022 55659022 + Missense_Mutation SNP G G A TCGA-G3-A5SL-01A-11D-A27I-10 TCGA-G3-A5SL-10A-01D-A27I-10 g.chr11:55659022G>A c.1273G>A c.(1273-1275)Gtt>Att p.V425I LUAD 11 55653015 55653015 + Silent SNP C C A TCGA-99-7458-01A-11D-2036-08 TCGA-99-7458-10A-01D-2036-08 g.chr11:55653015C>A c.111C>A c.(109-111)ccC>ccA p.P37P LUAD 11 55653024 55653024 + Nonsense_Mutation SNP C C G TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr11:55653024C>G c.120C>G c.(118-120)taC>taG p.Y40* LUAD 11 55653030 55653030 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr11:55653030C>A c.126C>A c.(124-126)aaC>aaA p.N42K LUAD 11 55653042 55653042 + Silent SNP G G A TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chr11:55653042G>A c.138G>A c.(136-138)acG>acA p.T46T LUAD 11 55653044 55653044 + Missense_Mutation SNP C C A TCGA-69-8255-01A-11D-2284-08 TCGA-69-8255-10A-01D-2284-08 g.chr11:55653044C>A c.140C>A c.(139-141)gCa>gAa p.A47E LUAD 11 55653094 55653094 + Missense_Mutation SNP C C T TCGA-17-Z043-01A-01W-0746-08 TCGA-17-Z043-11A-01W-0746-08 g.chr11:55653094C>T c.190C>T c.(190-192)Ctc>Ttc p.L64F LUAD 11 55653101 55653101 + Missense_Mutation SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr11:55653101C>A c.197C>A c.(196-198)aCt>aAt p.T66N LUAD 11 55653182 55653182 + Missense_Mutation SNP G G T TCGA-17-Z042-01A-01W-0746-08 TCGA-17-Z042-11A-01W-0746-08 g.chr11:55653182G>T c.278G>T c.(277-279)tGt>tTt p.C93F LUAD 11 55653223 55653223 + Missense_Mutation SNP G G C TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chr11:55653223G>C c.319G>C c.(319-321)Gac>Cac p.D107H LUAD 11 55653245 55653245 + Missense_Mutation SNP C C A TCGA-53-A4EZ-01A-12D-A24P-08 TCGA-53-A4EZ-10A-01D-A24P-08 g.chr11:55653245C>A c.341C>A c.(340-342)cCg>cAg p.P114Q LUAD 11 55653297 55653297 + Missense_Mutation SNP G G T TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr11:55653297G>T c.393G>T c.(391-393)tgG>tgT p.W131C LUAD 11 55653315 55653315 + Splice_Site SNP G G T TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr11:55653315G>T c.411G>T c.(409-411)cgG>cgT p.R137R LUAD 11 55653689 55653689 + Missense_Mutation SNP T T A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr11:55653689T>A c.502T>A c.(502-504)Tgg>Agg p.W168R LUAD 11 55653690 55653690 + Missense_Mutation SNP G G T TCGA-05-4415-01A-22D-1855-08 TCGA-05-4415-10A-01D-1855-08 g.chr11:55653690G>T c.503G>T c.(502-504)tGg>tTg p.W168L LUAD 11 55653694 55653694 + Splice_Site SNP G G T TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr11:55653694G>T c.507G>T c.(505-507)aaG>aaT p.K169N LUAD 11 55655571 55655571 + Missense_Mutation SNP C C A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr11:55655571C>A c.571C>A c.(571-573)Cat>Aat p.H191N LUAD 11 55655604 55655604 + Silent SNP C C A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr11:55655604C>A c.604C>A c.(604-606)Cga>Aga p.R202R LUAD 11 55655631 55655631 + Missense_Mutation SNP C C A TCGA-78-7535-01A-11D-2063-08 TCGA-78-7535-10A-01D-2063-08 g.chr11:55655631C>A c.631C>A c.(631-633)Caa>Aaa p.Q211K LUAD 11 55655667 55655667 + Silent SNP A A C TCGA-38-4630-01A-01D-1265-08 TCGA-38-4630-11A-01D-1265-08 g.chr11:55655667A>C c.667A>C c.(667-669)Agg>Cgg p.R223R LUAD 11 55655699 55655699 + Silent SNP G G T TCGA-17-Z055-01A-01W-0747-08 TCGA-17-Z055-11A-01W-0747-08 g.chr11:55655699G>T c.699G>T c.(697-699)ctG>ctT p.L233L LUAD 11 55655703 55655703 + Missense_Mutation SNP C C A TCGA-69-7973-01A-11D-2184-08 TCGA-69-7973-10A-01D-2184-08 g.chr11:55655703C>A c.703C>A c.(703-705)Caa>Aaa p.Q235K LUAD 11 55655715 55655715 + Missense_Mutation SNP A A G TCGA-78-7161-01A-11D-2036-08 TCGA-78-7161-10A-01D-2036-08 g.chr11:55655715A>G c.715A>G c.(715-717)Aaa>Gaa p.K239E LUAD 11 55657435 55657435 + Missense_Mutation SNP T T A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr11:55657435T>A c.779T>A c.(778-780)cTg>cAg p.L260Q LUAD 11 55657475 55657475 + Silent SNP G G T TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr11:55657475G>T c.819G>T c.(817-819)ggG>ggT p.G273G LUAD 11 55658649 55658649 + Silent SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr11:55658649C>A c.900C>A c.(898-900)atC>atA p.I300I LUAD 11 55658655 55658655 + Silent SNP G G C TCGA-MP-A4TA-01A-21D-A24P-08 TCGA-MP-A4TA-10A-01D-A24P-08 g.chr11:55658655G>C c.906G>C c.(904-906)ctG>ctC p.L302L LUAD 11 55658693 55658693 + Missense_Mutation SNP C C A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr11:55658693C>A c.944C>A c.(943-945)cCt>cAt p.P315H LUAD 11 55658697 55658697 + Silent SNP A A G TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr11:55658697A>G c.948A>G c.(946-948)caA>caG p.Q316Q LUAD 11 55658705 55658705 + Missense_Mutation SNP C C T TCGA-91-6836-01A-21D-1855-08 TCGA-91-6836-11A-01D-1855-08 g.chr11:55658705C>T c.956C>T c.(955-957)cCc>cTc p.P319L LUAD 11 55658737 55658737 + Missense_Mutation SNP G G T TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chr11:55658737G>T c.988G>T c.(988-990)Gta>Tta p.V330L LUAD 11 55658753 55658753 + Missense_Mutation SNP C C G TCGA-49-6745-01A-11D-1855-08 TCGA-49-6745-11A-01D-1855-08 g.chr11:55658753C>G c.1004C>G c.(1003-1005)gCt>gGt p.A335G LUAD 11 55658777 55658777 + Missense_Mutation SNP G G T TCGA-17-Z028-01A-01W-0746-08 TCGA-17-Z028-11A-01W-0746-08 g.chr11:55658777G>T c.1028G>T c.(1027-1029)tGg>tTg p.W343L LUAD 11 55658790 55658790 + Frame_Shift_Del DEL G G - TCGA-55-7724-01A-11D-2167-08 TCGA-55-7724-10A-01D-2167-08 g.chr11:55658790delG c.1041delG c.(1039-1041)atgfs p.M347fs LUAD 11 55658890 55658890 + Missense_Mutation SNP G G A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr11:55658890G>A c.1141G>A c.(1141-1143)Gga>Aga p.G381R LUAD 11 55658922 55658922 + Silent SNP C C A TCGA-78-7535-01A-11D-2063-08 TCGA-78-7535-10A-01D-2063-08 g.chr11:55658922C>A c.1173C>A c.(1171-1173)ctC>ctA p.L391L LUAD 11 55658932 55658932 + Missense_Mutation SNP T T A TCGA-73-4662-01A-01D-1265-08 TCGA-73-4662-11A-01D-1265-08 g.chr11:55658932T>A c.1183T>A c.(1183-1185)Tcc>Acc p.S395T LUAD 11 55658938 55658938 + Missense_Mutation SNP C C A TCGA-55-A491-01A-11D-A24D-08 TCGA-55-A491-10A-01D-A24F-08 g.chr11:55658938C>A c.1189C>A c.(1189-1191)Ctt>Att p.L397I LUAD 11 55658995 55658995 + Missense_Mutation SNP G G C TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr11:55658995G>C c.1246G>C c.(1246-1248)Gaa>Caa p.E416Q LUAD 11 55659000 55659000 + Silent SNP T T C TCGA-55-A491-01A-11D-A24D-08 TCGA-55-A491-10A-01D-A24F-08 g.chr11:55659000T>C c.1251T>C c.(1249-1251)ggT>ggC p.G417G LUAD 11 55659052 55659052 + Missense_Mutation SNP C C A TCGA-38-4626-01A-01D-1553-08 TCGA-38-4626-11A-01D-1553-08 g.chr11:55659052C>A c.1303C>A c.(1303-1305)Ccc>Acc p.P435T LUAD 11 55659073 55659073 + Missense_Mutation SNP C C A TCGA-O1-A52J-01A-11D-A25L-08 TCGA-O1-A52J-10A-01D-A25L-08 g.chr11:55659073C>A c.1324C>A c.(1324-1326)Cct>Act p.P442T LUAD 11 55659078 55659078 + Silent SNP C C A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr11:55659078C>A c.1329C>A c.(1327-1329)ctC>ctA p.L443L LUSC 11 55653687 55653687 + Missense_Mutation SNP G G T TCGA-85-6175-01A-11D-1817-08 TCGA-85-6175-10A-01D-1817-08 g.chr11:55653687G>T c.500G>T c.(499-501)tGc>tTc p.C167F LUSC 11 55655539 55655539 + Missense_Mutation SNP G G T TCGA-56-1622-01A-01D-1521-08 TCGA-56-1622-11A-01D-1521-08 g.chr11:55655539G>T c.539G>T c.(538-540)aGa>aTa p.R180I LUSC 11 55655543 55655543 + Silent SNP T T A TCGA-46-3767-01A-01D-0983-08 TCGA-46-3767-10A-01D-0983-08 g.chr11:55655543T>A c.543T>A c.(541-543)gcT>gcA p.A181A LUSC 11 55655595 55655595 + Missense_Mutation SNP G G C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr11:55655595G>C c.595G>C c.(595-597)Gaa>Caa p.E199Q LUSC 11 55655637 55655637 + Missense_Mutation SNP A A G TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr11:55655637A>G c.637A>G c.(637-639)Aat>Gat p.N213D LUSC 11 55655725 55655725 + Missense_Mutation SNP T T A TCGA-60-2713-01A-01D-1522-08 TCGA-60-2713-11A-01D-1522-08 g.chr11:55655725T>A c.725T>A c.(724-726)gTg>gAg p.V242E LUSC 11 55656477 55656477 + Splice_Site SNP G G T TCGA-18-5592-01A-01D-1632-08 TCGA-18-5592-11A-11D-1632-08 g.chr11:55656477G>T c.761G>T c.(760-762)aGg>aTg p.R254M LUSC 11 55657463 55657463 + Missense_Mutation SNP G G T TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr11:55657463G>T c.807G>T c.(805-807)gaG>gaT p.E269D LUSC 11 55657498 55657498 + Missense_Mutation SNP G G A TCGA-18-3417-01A-01D-1441-08 TCGA-18-3417-11A-01D-1441-08 g.chr11:55657498G>A c.842G>A c.(841-843)aGc>aAc p.S281N LUSC 11 55657502 55657502 + Silent SNP C C A TCGA-18-4721-01A-01D-1441-08 TCGA-18-4721-11A-01D-1441-08 g.chr11:55657502C>A c.846C>A c.(844-846)ctC>ctA p.L282L LUSC 11 55658796 55658796 + Missense_Mutation SNP C C A TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr11:55658796C>A c.1047C>A c.(1045-1047)gaC>gaA p.D349E LUSC 11 55658883 55658883 + Silent SNP T T C TCGA-66-2780-01A-01D-1522-08 TCGA-66-2780-11A-01D-1522-08 g.chr11:55658883T>C c.1134T>C c.(1132-1134)ttT>ttC p.F378F LUSC 11 55658946 55658946 + Silent SNP G G A TCGA-46-6025-01A-11D-1817-08 TCGA-46-6025-10A-01D-1817-08 g.chr11:55658946G>A c.1197G>A c.(1195-1197)gtG>gtA p.V399V OV 11 55652991 55652991 + Missense_Mutation SNP C C G TCGA-30-1718-01A-01W-0633-09 TCGA-30-1718-10A-01W-0633-09 g.chr11:55652991C>G c.87C>G c.(85-87)gaC>gaG p.D29E OV 11 55653305 55653305 + Missense_Mutation SNP A A T TCGA-24-1436-01A-01W-0549-09 TCGA-24-1436-10A-01W-0549-09 g.chr11:55653305A>T c.401A>T c.(400-402)gAg>gTg p.E134V OV 11 55655589 55655589 + Missense_Mutation SNP C C T TCGA-29-1761-01A-01W-0633-09 TCGA-29-1761-10A-01W-0633-09 g.chr11:55655589C>T c.589C>T c.(589-591)Cac>Tac p.H197Y PAAD 11 55653623 55653623 + Missense_Mutation SNP T T C TCGA-FB-A78T-01A-12D-A32N-08 TCGA-FB-A78T-10A-01D-A32N-08 g.chr11:55653623T>C c.436T>C c.(436-438)Tct>Cct p.S146P PAAD 11 55655602 55655602 + Missense_Mutation SNP T T A TCGA-3A-A9IC-01A-11D-A38G-08 TCGA-3A-A9IC-10A-01D-A38J-08 g.chr11:55655602T>A c.602T>A c.(601-603)cTg>cAg p.L201Q PAAD 11 55658776 55658776 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:55658776T>C c.1027T>C c.(1027-1029)Tgg>Cgg p.W343R PAAD 11 55658916 55658916 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:55658916C>T c.1167C>T c.(1165-1167)tgC>tgT p.C389C PCPG 11 55653270 55653270 + Silent SNP G G A TCGA-QR-A70K-01A-12D-A35D-08 TCGA-QR-A70K-10A-01D-A35B-08 g.chr11:55653270G>A c.366G>A c.(364-366)cgG>cgA p.R122R PRAD 11 55652923 55652923 + Missense_Mutation SNP C C A TCGA-TP-A8TV-01A-11D-A41K-08 TCGA-TP-A8TV-10A-01D-A41N-08 g.chr11:55652923C>A c.19C>A c.(19-21)Caa>Aaa p.Q7K PRAD 11 55653269 55653269 + Missense_Mutation SNP G G A TCGA-X4-A8KQ-01A-12D-A364-08 TCGA-X4-A8KQ-10A-01D-A362-08 g.chr11:55653269G>A c.365G>A c.(364-366)cGg>cAg p.R122Q PRAD 11 55658642 55658642 + Missense_Mutation SNP G G C TCGA-VN-A88N-01A-11D-A364-08 TCGA-VN-A88N-10B-01D-A362-08 g.chr11:55658642G>C c.893G>C c.(892-894)aGt>aCt p.S298T PRAD 11 55659088 55659088 + Missense_Mutation SNP T T A TCGA-ZG-A9N3-01A-11D-A41K-08 TCGA-ZG-A9N3-10A-01D-A41N-08 g.chr11:55659088T>A c.1339T>A c.(1339-1341)Ttt>Att p.F447I READ 11 55658984 55658984 + Missense_Mutation SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:55658984T>C c.1235T>C c.(1234-1236)tTc>tCc p.F412S SKCM 11 55652961 55652961 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:55652961G>A c.57G>A c.(55-57)atG>atA p.M19I SKCM 11 55652968 55652968 + Missense_Mutation SNP T T C TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr11:55652968T>C c.64T>C c.(64-66)Ttc>Ctc p.F22L SKCM 11 55652970 55652970 + Silent SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr11:55652970C>T c.66C>T c.(64-66)ttC>ttT p.F22F SKCM 11 55653012 55653012 + Silent SNP G G A TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr11:55653012G>A c.108G>A c.(106-108)cgG>cgA p.R36R SKCM 11 55653172 55653172 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr11:55653172G>A c.268G>A c.(268-270)Gag>Aag p.E90K SKCM 11 55653186 55653186 + Silent SNP G G A TCGA-EE-A2GT-06A-12D-A197-08 TCGA-EE-A2GT-10A-01D-A199-08 g.chr11:55653186G>A c.282G>A c.(280-282)ggG>ggA p.G94G SKCM 11 55653197 55653197 + Missense_Mutation SNP A A T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:55653197A>T c.293A>T c.(292-294)gAg>gTg p.E98V SKCM 11 55653274 55653274 + Missense_Mutation SNP C C T TCGA-EE-A2MU-06A-21D-A196-08 TCGA-EE-A2MU-10A-01D-A198-08 g.chr11:55653274C>T c.370C>T c.(370-372)Cac>Tac p.H124Y SKCM 11 55653307 55653307 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:55653307G>A c.403G>A c.(403-405)Gaa>Aaa p.E135K SKCM 11 55653314 55653314 + Splice_Site SNP G G A TCGA-EE-A3J8-06A-11D-A20D-08 TCGA-EE-A3J8-10A-01D-A20D-08 g.chr11:55653314G>A c.410G>A c.(409-411)cGg>cAg p.R137Q SKCM 11 55653632 55653632 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:55653632G>A c.445G>A c.(445-447)Gaa>Aaa p.E149K SKCM 11 55655529 55655529 + Missense_Mutation SNP G G A TCGA-EE-A2ML-06A-11D-A197-08 TCGA-EE-A2ML-10A-01D-A199-08 g.chr11:55655529G>A c.529G>A c.(529-531)Gaa>Aaa p.E177K SKCM 11 55655574 55655574 + Missense_Mutation SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr11:55655574G>A c.574G>A c.(574-576)Gaa>Aaa p.E192K SKCM 11 55655577 55655577 + Missense_Mutation SNP G G A TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr11:55655577G>A c.577G>A c.(577-579)Gaa>Aaa p.E193K SKCM 11 55655605 55655605 + Missense_Mutation SNP G G A TCGA-FS-A4F9-06A-11D-A24R-08 TCGA-FS-A4F9-10A-01D-A24R-08 g.chr11:55655605G>A c.605G>A c.(604-606)cGa>cAa p.R202Q SKCM 11 55655605 55655605 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:55655605G>A c.605G>A c.(604-606)cGa>cAa p.R202Q SKCM 11 55655610 55655610 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:55655610G>A c.610G>A c.(610-612)Gag>Aag p.E204K SKCM 11 55655644 55655644 + Missense_Mutation SNP G G A TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr11:55655644G>A c.644G>A c.(643-645)aGc>aAc p.S215N SKCM 11 55658717 55658717 + Missense_Mutation SNP G G A TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr11:55658717G>A c.968G>A c.(967-969)gGa>gAa p.G323E SKCM 11 55658779 55658779 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:55658779G>A c.1030G>A c.(1030-1032)Gag>Aag p.E344K SKCM 11 55658834 55658834 + Nonsense_Mutation SNP G G A TCGA-ER-A19J-06A-11D-A196-08 TCGA-ER-A19J-10A-01D-A198-08 g.chr11:55658834G>A c.1085G>A c.(1084-1086)tGg>tAg p.W362*

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 11 55658765 55658765 single base substitution G T missense_variant G196V 587G>T BLCA-CN 11 55658765 55658765 single base substitution G T missense_variant G339V 1016G>T BLCA-US 11 55653304 55653304 single base substitution G T stop_gained E134* 400G>T BLCA-US 11 55653304 55653304 single base substitution G T upstream_gene_variant BLCA-US 11 55658689 55658689 single base substitution G C missense_variant D171H 511G>C BLCA-US 11 55658689 55658689 single base substitution G C missense_variant D314H 940G>C BLCA-US 11 55658785 55658785 single base substitution C T missense_variant H203Y 607C>T BLCA-US 11 55658785 55658785 single base substitution C T missense_variant H346Y 1036C>T BOCA-FR 11 55648321 55648321 single base substitution C A upstream_gene_variant BOCA-FR 11 55651150 55651150 single base substitution A T intron_variant BOCA-FR 11 55651150 55651150 single base substitution A T upstream_gene_variant BOCA-FR 11 55656776 55656776 single base substitution A T intron_variant BOCA-FR 11 55663465 55663465 single base substitution C T downstream_gene_variant BRCA-EU 11 55647525 55647525 single base substitution T G upstream_gene_variant BRCA-EU 11 55647603 55647603 single base substitution C A upstream_gene_variant BRCA-EU 11 55647734 55647734 single base substitution G C upstream_gene_variant BRCA-EU 11 55648219 55648219 single base substitution T C upstream_gene_variant BRCA-EU 11 55648386 55648386 single base substitution T A upstream_gene_variant BRCA-EU 11 55648846 55648846 single base substitution A G upstream_gene_variant BRCA-EU 11 55649315 55649315 single base substitution A T upstream_gene_variant BRCA-EU 11 55649828 55649828 single base substitution G A upstream_gene_variant BRCA-EU 11 55650315 55650315 single base substitution C A upstream_gene_variant BRCA-EU 11 55650440 55650440 single base substitution A T upstream_gene_variant BRCA-EU 11 55650492 55650492 single base substitution G C upstream_gene_variant BRCA-EU 11 55650896 55650896 single base substitution C T intron_variant BRCA-EU 11 55650896 55650896 single base substitution C T upstream_gene_variant BRCA-EU 11 55650956 55650956 single base substitution G A intron_variant BRCA-EU 11 55650956 55650956 single base substitution G A upstream_gene_variant BRCA-EU 11 55651115 55651115 single base substitution G A intron_variant BRCA-EU 11 55651115 55651115 single base substitution G A upstream_gene_variant BRCA-EU 11 55651601 55651601 single base substitution C G intron_variant BRCA-EU 11 55651601 55651601 single base substitution C G upstream_gene_variant BRCA-EU 11 55652472 55652472 single base substitution T C intron_variant BRCA-EU 11 55652472 55652472 single base substitution T C upstream_gene_variant BRCA-EU 11 55652786 55652786 single base substitution G A intron_variant BRCA-EU 11 55652786 55652786 single base substitution G A upstream_gene_variant BRCA-EU 11 55653392 55653392 single base substitution A G intron_variant BRCA-EU 11 55653392 55653392 single base substitution A G upstream_gene_variant BRCA-EU 11 55653861 55653861 single base substitution C G intron_variant BRCA-EU 11 55655865 55655865 single base substitution A T intron_variant BRCA-EU 11 55655914 55655914 single base substitution C T intron_variant BRCA-EU 11 55656143 55656143 single base substitution T C intron_variant BRCA-EU 11 55656247 55656247 single base substitution C T intron_variant BRCA-EU 11 55656267 55656267 single base substitution C G intron_variant BRCA-EU 11 55657362 55657362 deletion of <=200bp T - intron_variant BRCA-EU 11 55658104 55658104 single base substitution C T intron_variant BRCA-EU 11 55658744 55658744 single base substitution G C missense_variant G189A 566G>C BRCA-EU 11 55658744 55658744 single base substitution G C missense_variant G332A 995G>C BRCA-EU 11 55659463 55659463 single base substitution C T downstream_gene_variant BRCA-EU 11 55659528 55659528 single base substitution A G downstream_gene_variant BRCA-EU 11 55660615 55660615 single base substitution G A downstream_gene_variant BRCA-EU 11 55660749 55660749 insertion of <=200bp - TT downstream_gene_variant BRCA-EU 11 55660915 55660915 single base substitution G A downstream_gene_variant BRCA-EU 11 55660917 55660917 single base substitution T C downstream_gene_variant BRCA-EU 11 55660954 55660954 single base substitution T C downstream_gene_variant BRCA-EU 11 55661042 55661042 single base substitution C A downstream_gene_variant BRCA-EU 11 55661392 55661392 single base substitution C A downstream_gene_variant BRCA-EU 11 55662395 55662395 single base substitution C A downstream_gene_variant BRCA-EU 11 55663786 55663786 deletion of <=200bp T - downstream_gene_variant BRCA-EU 11 55663822 55663822 single base substitution G T downstream_gene_variant BRCA-EU 11 55664068 55664068 single base substitution A G downstream_gene_variant BRCA-FR 11 55650896 55650896 single base substitution C T intron_variant BRCA-FR 11 55650896 55650896 single base substitution C T upstream_gene_variant BRCA-FR 11 55650956 55650956 single base substitution G A intron_variant BRCA-FR 11 55650956 55650956 single base substitution G A upstream_gene_variant BRCA-FR 11 55657043 55657043 single base substitution G A intron_variant BRCA-FR 11 55657059 55657059 single base substitution G A intron_variant BRCA-FR 11 55657795 55657795 single base substitution A C intron_variant BRCA-FR 11 55657827 55657827 single base substitution T C intron_variant BRCA-FR 11 55659463 55659463 single base substitution C T downstream_gene_variant BRCA-FR 11 55663772 55663772 single base substitution A G downstream_gene_variant BRCA-UK 11 55652922 55652922 single base substitution G T missense_variant L6F 18G>T BRCA-UK 11 55652922 55652922 single base substitution G T upstream_gene_variant BRCA-UK 11 55653198 55653198 single base substitution G T missense_variant E98D 294G>T BRCA-UK 11 55653198 55653198 single base substitution G T upstream_gene_variant BRCA-UK 11 55654573 55654573 single base substitution T G intron_variant BRCA-UK 11 55654621 55654621 single base substitution A C intron_variant BRCA-US 11 55653610 55653610 deletion of <=200bp A - 5_prime_UTR_variant BRCA-US 11 55653610 55653610 deletion of <=200bp A - frameshift_variant L141 BRCA-US 11 55653691 55653691 single base substitution G A stop_gained W168* 504G>A BRCA-US 11 55653691 55653691 single base substitution G A stop_gained W25* 75G>A BRCA-US 11 55657466 55657466 single base substitution C T synonymous_variant L127L 381C>T BRCA-US 11 55657466 55657466 single base substitution C T synonymous_variant L270L 810C>T BRCA-US 11 55658869 55658869 single base substitution G A missense_variant E231K 691G>A BRCA-US 11 55658869 55658869 single base substitution G A missense_variant E374K 1120G>A BTCA-JP 11 55653610 55653610 deletion of <=200bp A - 5_prime_UTR_variant BTCA-JP 11 55653610 55653610 deletion of <=200bp A - frameshift_variant L141 CESC-US 11 55653082 55653082 single base substitution C T missense_variant R60W 178C>T CESC-US 11 55653082 55653082 single base substitution C T upstream_gene_variant CESC-US 11 55653304 55653304 single base substitution G A missense_variant E134K 400G>A CESC-US 11 55653304 55653304 single base substitution G A upstream_gene_variant CESC-US 11 55658629 55658629 single base substitution G A missense_variant E151K 451G>A CESC-US 11 55658629 55658629 single base substitution G A missense_variant E294K 880G>A CLLE-ES 11 55645894 55645894 single base substitution C T upstream_gene_variant CLLE-ES 11 55652610 55652610 single base substitution C T intron_variant CLLE-ES 11 55652610 55652610 single base substitution C T upstream_gene_variant CLLE-ES 11 55655397 55655397 single base substitution A G intron_variant COAD-US 11 55652963 55652963 single base substitution A G missense_variant N20S 59A>G COAD-US 11 55652963 55652963 single base substitution A G upstream_gene_variant COAD-US 11 55653041 55653041 single base substitution C T missense_variant T46M 137C>T COAD-US 11 55653041 55653041 single base substitution C T upstream_gene_variant COAD-US 11 55653081 55653081 single base substitution G A synonymous_variant T59T 177G>A COAD-US 11 55653081 55653081 single base substitution G A upstream_gene_variant COAD-US 11 55653129 55653129 single base substitution C T synonymous_variant F75F 225C>T COAD-US 11 55653129 55653129 single base substitution C T upstream_gene_variant COAD-US 11 55655586 55655586 single base substitution C T missense_variant H196Y 586C>T COAD-US 11 55655586 55655586 single base substitution C T missense_variant H53Y 157C>T COAD-US 11 55655682 55655682 single base substitution G T stop_gained G228* 682G>T COAD-US 11 55655682 55655682 single base substitution G T stop_gained G85* 253G>T COAD-US 11 55655737 55655737 single base substitution A T missense_variant Q103L 308A>T COAD-US 11 55655737 55655737 single base substitution A T missense_variant Q246L 737A>T COAD-US 11 55657450 55657450 single base substitution C A missense_variant P122H 365C>A COAD-US 11 55657450 55657450 single base substitution C A missense_variant P265H 794C>A COAD-US 11 55658706 55658706 single base substitution C T synonymous_variant P176P 528C>T COAD-US 11 55658706 55658706 single base substitution C T synonymous_variant P319P 957C>T COAD-US 11 55659006 55659006 single base substitution C A synonymous_variant T276T 828C>A COAD-US 11 55659006 55659006 single base substitution C A synonymous_variant T419T 1257C>A COCA-CN 11 55656396 55656396 single base substitution T G intron_variant COCA-CN 11 55656440 55656440 single base substitution T A intron_variant COCA-CN 11 55657556 55657556 single base substitution C A intron_variant COCA-CN 11 55658734 55658734 single base substitution C A missense_variant L186I 556C>A COCA-CN 11 55658734 55658734 single base substitution C A missense_variant L329I 985C>A EOPC-DE 11 55656745 55656745 single base substitution A G intron_variant ESAD-UK 11 55646000 55646000 single base substitution T C upstream_gene_variant ESAD-UK 11 55646164 55646164 single base substitution T A upstream_gene_variant ESAD-UK 11 55646258 55646258 single base substitution C G upstream_gene_variant ESAD-UK 11 55646779 55646779 single base substitution A C upstream_gene_variant ESAD-UK 11 55646978 55646978 single base substitution T G upstream_gene_variant ESAD-UK 11 55647011 55647011 single base substitution T C upstream_gene_variant ESAD-UK 11 55647131 55647131 single base substitution A C upstream_gene_variant ESAD-UK 11 55647447 55647447 single base substitution C A upstream_gene_variant ESAD-UK 11 55647457 55647457 single base substitution C A upstream_gene_variant ESAD-UK 11 55647904 55647904 single base substitution A G upstream_gene_variant ESAD-UK 11 55648368 55648368 single base substitution T A upstream_gene_variant ESAD-UK 11 55648631 55648631 single base substitution T G upstream_gene_variant ESAD-UK 11 55648633 55648633 single base substitution G A upstream_gene_variant ESAD-UK 11 55648941 55648941 single base substitution A T upstream_gene_variant ESAD-UK 11 55648989 55648989 single base substitution T C upstream_gene_variant ESAD-UK 11 55649846 55649846 single base substitution C A upstream_gene_variant ESAD-UK 11 55650361 55650361 single base substitution T G upstream_gene_variant ESAD-UK 11 55650710 55650710 single base substitution T C upstream_gene_variant ESAD-UK 11 55652115 55652115 single base substitution G A intron_variant ESAD-UK 11 55652115 55652115 single base substitution G A upstream_gene_variant ESAD-UK 11 55652327 55652327 single base substitution C G intron_variant ESAD-UK 11 55652327 55652327 single base substitution C G upstream_gene_variant ESAD-UK 11 55652403 55652403 single base substitution G T intron_variant ESAD-UK 11 55652403 55652403 single base substitution G T upstream_gene_variant ESAD-UK 11 55652642 55652642 single base substitution T G intron_variant ESAD-UK 11 55652642 55652642 single base substitution T G upstream_gene_variant ESAD-UK 11 55652755 55652755 single base substitution T G intron_variant ESAD-UK 11 55652755 55652755 single base substitution T G upstream_gene_variant ESAD-UK 11 55652799 55652799 single base substitution G T intron_variant ESAD-UK 11 55652799 55652799 single base substitution G T upstream_gene_variant ESAD-UK 11 55652956 55652956 single base substitution T C missense_variant C18R 52T>C ESAD-UK 11 55652956 55652956 single base substitution T C upstream_gene_variant ESAD-UK 11 55653074 55653074 single base substitution A G missense_variant K57R 170A>G ESAD-UK 11 55653074 55653074 single base substitution A G upstream_gene_variant ESAD-UK 11 55653119 55653119 single base substitution A C missense_variant N72T 215A>C ESAD-UK 11 55653119 55653119 single base substitution A C upstream_gene_variant ESAD-UK 11 55653141 55653141 single base substitution A T missense_variant K79N 237A>T ESAD-UK 11 55653141 55653141 single base substitution A T upstream_gene_variant ESAD-UK 11 55653309 55653309 single base substitution A T missense_variant E135D 405A>T ESAD-UK 11 55653309 55653309 single base substitution A T upstream_gene_variant ESAD-UK 11 55653550 55653550 single base substitution T A 5_prime_UTR_variant ESAD-UK 11 55653550 55653550 single base substitution T A intron_variant ESAD-UK 11 55653610 55653610 deletion of <=200bp A - 5_prime_UTR_variant ESAD-UK 11 55653610 55653610 deletion of <=200bp A - frameshift_variant L141 ESAD-UK 11 55653655 55653655 single base substitution A G synonymous_variant R13R 39A>G ESAD-UK 11 55653655 55653655 single base substitution A G synonymous_variant R156R 468A>G ESAD-UK 11 55653680 55653680 single base substitution A C missense_variant T165P 493A>C ESAD-UK 11 55653680 55653680 single base substitution A C missense_variant T22P 64A>C ESAD-UK 11 55654432 55654432 single base substitution T G intron_variant ESAD-UK 11 55654451 55654451 single base substitution A C intron_variant ESAD-UK 11 55654711 55654711 single base substitution T C intron_variant ESAD-UK 11 55655436 55655436 single base substitution T G intron_variant ESAD-UK 11 55655461 55655461 single base substitution A G intron_variant ESAD-UK 11 55656256 55656256 single base substitution T C intron_variant ESAD-UK 11 55656595 55656595 single base substitution T G intron_variant ESAD-UK 11 55656608 55656608 single base substitution C T intron_variant ESAD-UK 11 55656831 55656831 single base substitution C T intron_variant ESAD-UK 11 55656966 55656966 single base substitution G A intron_variant ESAD-UK 11 55657031 55657031 single base substitution C A intron_variant ESAD-UK 11 55657163 55657163 single base substitution A C intron_variant ESAD-UK 11 55657230 55657230 single base substitution A G intron_variant ESAD-UK 11 55657239 55657239 single base substitution T A intron_variant ESAD-UK 11 55657845 55657845 single base substitution T G intron_variant ESAD-UK 11 55658153 55658153 single base substitution A C intron_variant ESAD-UK 11 55658347 55658347 single base substitution G T intron_variant ESAD-UK 11 55658348 55658348 single base substitution G T intron_variant ESAD-UK 11 55658384 55658384 single base substitution T A intron_variant ESAD-UK 11 55658384 55658384 single base substitution T G intron_variant ESAD-UK 11 55658404 55658404 single base substitution T G intron_variant ESAD-UK 11 55658706 55658706 single base substitution C A synonymous_variant P176P 528C>A ESAD-UK 11 55658706 55658706 single base substitution C A synonymous_variant P319P 957C>A ESAD-UK 11 55659013 55659013 single base substitution T C missense_variant F279L 835T>C ESAD-UK 11 55659013 55659013 single base substitution T C missense_variant F422L 1264T>C ESAD-UK 11 55659067 55659067 single base substitution T C missense_variant S297P 889T>C ESAD-UK 11 55659067 55659067 single base substitution T C missense_variant S440P 1318T>C ESAD-UK 11 55659075 55659075 single base substitution T C synonymous_variant P299P 897T>C ESAD-UK 11 55659075 55659075 single base substitution T C synonymous_variant P442P 1326T>C ESAD-UK 11 55659164 55659164 single base substitution A C 3_prime_UTR_variant ESAD-UK 11 55659244 55659244 single base substitution C T 3_prime_UTR_variant ESAD-UK 11 55659472 55659472 single base substitution A C downstream_gene_variant ESAD-UK 11 55659870 55659870 single base substitution A C downstream_gene_variant ESAD-UK 11 55659889 55659889 single base substitution A C downstream_gene_variant ESAD-UK 11 55659942 55659942 single base substitution A C downstream_gene_variant ESAD-UK 11 55660107 55660107 single base substitution A C downstream_gene_variant ESAD-UK 11 55660580 55660580 single base substitution T G downstream_gene_variant ESAD-UK 11 55660669 55660669 single base substitution T G downstream_gene_variant ESAD-UK 11 55660717 55660717 single base substitution G T downstream_gene_variant ESAD-UK 11 55660813 55660813 single base substitution G C downstream_gene_variant ESAD-UK 11 55661078 55661078 single base substitution C T downstream_gene_variant ESAD-UK 11 55661117 55661117 single base substitution T C downstream_gene_variant ESAD-UK 11 55661452 55661452 single base substitution A C downstream_gene_variant ESAD-UK 11 55661558 55661558 single base substitution T C downstream_gene_variant ESAD-UK 11 55661718 55661718 single base substitution A C downstream_gene_variant ESAD-UK 11 55661759 55661759 single base substitution A C downstream_gene_variant ESAD-UK 11 55661844 55661844 single base substitution T G downstream_gene_variant ESAD-UK 11 55661895 55661895 single base substitution T C downstream_gene_variant ESAD-UK 11 55661973 55661973 single base substitution A G downstream_gene_variant ESAD-UK 11 55662111 55662111 single base substitution A G downstream_gene_variant ESAD-UK 11 55662111 55662111 single base substitution A T downstream_gene_variant ESAD-UK 11 55662557 55662557 single base substitution T G downstream_gene_variant ESAD-UK 11 55662608 55662608 single base substitution A T downstream_gene_variant ESAD-UK 11 55662797 55662797 single base substitution T C downstream_gene_variant ESAD-UK 11 55662910 55662910 single base substitution A G downstream_gene_variant ESAD-UK 11 55663077 55663077 single base substitution A C downstream_gene_variant ESAD-UK 11 55663219 55663219 single base substitution T G downstream_gene_variant ESAD-UK 11 55663760 55663760 single base substitution T C downstream_gene_variant ESAD-UK 11 55663790 55663790 single base substitution T G downstream_gene_variant ESAD-UK 11 55664017 55664017 single base substitution A T downstream_gene_variant ESAD-UK 11 55664020 55664020 single base substitution T G downstream_gene_variant ESAD-UK 11 55664058 55664058 single base substitution A C downstream_gene_variant ESAD-UK 11 55664089 55664089 single base substitution A C downstream_gene_variant ESCA-CN 11 55653871 55653871 single base substitution A T intron_variant ESCA-CN 11 55656595 55656595 single base substitution T C intron_variant ESCA-CN 11 55658038 55658038 single base substitution C A intron_variant ESCA-CN 11 55658914 55658914 single base substitution T C missense_variant C246R 736T>C ESCA-CN 11 55658914 55658914 single base substitution T C missense_variant C389R 1165T>C GBM-US 11 55652963 55652963 single base substitution A G missense_variant N20S 59A>G GBM-US 11 55652963 55652963 single base substitution A G upstream_gene_variant GBM-US 11 55653041 55653041 single base substitution C T missense_variant T46M 137C>T GBM-US 11 55653041 55653041 single base substitution C T upstream_gene_variant GBM-US 11 55653246 55653246 single base substitution G A synonymous_variant P114P 342G>A GBM-US 11 55653246 55653246 single base substitution G A upstream_gene_variant GBM-US 11 55653609 55653609 insertion of <=200bp - A 5_prime_UTR_variant GBM-US 11 55653609 55653609 insertion of <=200bp - A frameshift_variant L141H? GBM-US 11 55655555 55655555 single base substitution G T missense_variant K185N 555G>T GBM-US 11 55655555 55655555 single base substitution G T missense_variant K42N 126G>T GBM-US 11 55655591 55655591 single base substitution C A missense_variant H197Q 591C>A GBM-US 11 55655591 55655591 single base substitution C A missense_variant H54Q 162C>A KIRC-US 11 55653066 55653066 single base substitution A T missense_variant E54D 162A>T KIRC-US 11 55653066 55653066 single base substitution A T upstream_gene_variant KIRC-US 11 55653105 55653105 single base substitution C A missense_variant D67E 201C>A KIRC-US 11 55653105 55653105 single base substitution C A upstream_gene_variant KIRC-US 11 55653110 55653110 single base substitution G A missense_variant C69Y 206G>A KIRC-US 11 55653110 55653110 single base substitution G A upstream_gene_variant KIRC-US 11 55653128 55653128 single base substitution T A missense_variant F75Y 224T>A KIRC-US 11 55653128 55653128 single base substitution T A upstream_gene_variant KIRC-US 11 55658689 55658689 single base substitution G T missense_variant D171Y 511G>T KIRC-US 11 55658689 55658689 single base substitution G T missense_variant D314Y 940G>T KIRP-US 11 55658774 55658774 single base substitution A G missense_variant Y199C 596A>G KIRP-US 11 55658774 55658774 single base substitution A G missense_variant Y342C 1025A>G LAML-KR 11 55656479 55656479 single base substitution T G splice_donor_variant LGG-US 11 55653034 55653034 single base substitution C T stop_gained Q44* 130C>T LGG-US 11 55653034 55653034 single base substitution C T upstream_gene_variant LGG-US 11 55653246 55653246 single base substitution G A synonymous_variant P114P 342G>A LGG-US 11 55653246 55653246 single base substitution G A upstream_gene_variant LGG-US 11 55655604 55655604 single base substitution C T stop_gained R202* 604C>T LGG-US 11 55655604 55655604 single base substitution C T stop_gained R59* 175C>T LGG-US 11 55659044 55659044 single base substitution A T missense_variant Y289F 866A>T LGG-US 11 55659044 55659044 single base substitution A T missense_variant Y432F 1295A>T LICA-FR 11 55655883 55655883 single base substitution G T intron_variant LICA-FR 11 55662655 55662655 single base substitution T A downstream_gene_variant LIHC-US 11 55653258 55653258 single base substitution T C synonymous_variant S118S 354T>C LIHC-US 11 55653258 55653258 single base substitution T C upstream_gene_variant LIHC-US 11 55657422 55657422 single base substitution G A missense_variant E113K 337G>A LIHC-US 11 55657422 55657422 single base substitution G A missense_variant E256K 766G>A LIHC-US 11 55659022 55659022 single base substitution G A missense_variant V282I 844G>A LIHC-US 11 55659022 55659022 single base substitution G A missense_variant V425I 1273G>A LINC-JP 11 55648007 55648007 single base substitution T A upstream_gene_variant LINC-JP 11 55648690 55648690 single base substitution C T upstream_gene_variant LINC-JP 11 55648692 55648692 single base substitution C T upstream_gene_variant LINC-JP 11 55648714 55648714 single base substitution C T upstream_gene_variant LINC-JP 11 55648842 55648842 single base substitution C T upstream_gene_variant LINC-JP 11 55650193 55650193 single base substitution G C upstream_gene_variant LINC-JP 11 55652033 55652033 single base substitution G A intron_variant LINC-JP 11 55652033 55652033 single base substitution G A upstream_gene_variant LINC-JP 11 55652906 55652906 single base substitution T A start_lost M1K 2T>A LINC-JP 11 55652906 55652906 single base substitution T A upstream_gene_variant LINC-JP 11 55652928 55652928 single base substitution C T synonymous_variant V8V 24C>T LINC-JP 11 55652928 55652928 single base substitution C T upstream_gene_variant LINC-JP 11 55654006 55654006 single base substitution C A intron_variant LINC-JP 11 55655799 55655799 single base substitution C G intron_variant LINC-JP 11 55655821 55655821 single base substitution C G intron_variant LINC-JP 11 55656705 55656705 single base substitution A G intron_variant LINC-JP 11 55657174 55657174 single base substitution C G intron_variant LINC-JP 11 55657834 55657834 single base substitution A C intron_variant LINC-JP 11 55658342 55658342 single base substitution A G intron_variant LINC-JP 11 55659523 55659523 single base substitution A T downstream_gene_variant LIRI-JP 11 55646677 55646677 single base substitution C A upstream_gene_variant LIRI-JP 11 55647712 55647712 single base substitution A T upstream_gene_variant LIRI-JP 11 55648925 55648925 single base substitution T G upstream_gene_variant LIRI-JP 11 55649177 55649177 single base substitution T C upstream_gene_variant LIRI-JP 11 55649987 55649987 single base substitution T C upstream_gene_variant LIRI-JP 11 55650427 55650427 single base substitution G T upstream_gene_variant LIRI-JP 11 55650774 55650774 single base substitution C A 5_prime_UTR_variant LIRI-JP 11 55650774 55650774 single base substitution C A upstream_gene_variant LIRI-JP 11 55651262 55651262 single base substitution G A intron_variant LIRI-JP 11 55651262 55651262 single base substitution G A upstream_gene_variant LIRI-JP 11 55651682 55651682 single base substitution T C intron_variant LIRI-JP 11 55651682 55651682 single base substitution T C upstream_gene_variant LIRI-JP 11 55652419 55652419 single base substitution G T intron_variant LIRI-JP 11 55652419 55652419 single base substitution G T upstream_gene_variant LIRI-JP 11 55652722 55652722 single base substitution C A intron_variant LIRI-JP 11 55652722 55652722 single base substitution C A upstream_gene_variant LIRI-JP 11 55653178 55653178 single base substitution A G missense_variant I92V 274A>G LIRI-JP 11 55653178 55653178 single base substitution A G upstream_gene_variant LIRI-JP 11 55653190 55653190 single base substitution C T missense_variant H96Y 286C>T LIRI-JP 11 55653190 55653190 single base substitution C T upstream_gene_variant LIRI-JP 11 55653358 55653358 deletion of <=200bp G - intron_variant LIRI-JP 11 55653358 55653358 deletion of <=200bp G - upstream_gene_variant LIRI-JP 11 55655967 55655967 single base substitution G A intron_variant LIRI-JP 11 55656223 55656223 single base substitution T C intron_variant LIRI-JP 11 55656242 55656242 single base substitution A T intron_variant LIRI-JP 11 55656298 55656298 single base substitution G A intron_variant LIRI-JP 11 55656410 55656410 single base substitution A G intron_variant LIRI-JP 11 55656587 55656587 single base substitution G T intron_variant LIRI-JP 11 55656854 55656854 single base substitution A G intron_variant LIRI-JP 11 55657598 55657598 single base substitution A G intron_variant LIRI-JP 11 55657660 55657660 single base substitution T C intron_variant LIRI-JP 11 55657753 55657753 single base substitution T A intron_variant LIRI-JP 11 55658472 55658472 single base substitution T C intron_variant LIRI-JP 11 55661268 55661268 single base substitution C A downstream_gene_variant LIRI-JP 11 55661666 55661666 single base substitution G T downstream_gene_variant LIRI-JP 11 55661730 55661730 single base substitution C A downstream_gene_variant LIRI-JP 11 55662223 55662223 single base substitution G A downstream_gene_variant LIRI-JP 11 55662438 55662438 single base substitution C A downstream_gene_variant LIRI-JP 11 55662442 55662442 single base substitution T C downstream_gene_variant LIRI-JP 11 55663190 55663190 single base substitution A G downstream_gene_variant LIRI-JP 11 55663641 55663641 single base substitution T A downstream_gene_variant LIRI-JP 11 55664213 55664213 single base substitution G T downstream_gene_variant LUSC-KR 11 55646180 55646180 single base substitution G C upstream_gene_variant LUSC-KR 11 55646323 55646323 single base substitution T C upstream_gene_variant LUSC-KR 11 55646402 55646402 single base substitution A G upstream_gene_variant LUSC-KR 11 55648270 55648270 single base substitution T C upstream_gene_variant LUSC-KR 11 55648948 55648948 single base substitution A G upstream_gene_variant LUSC-KR 11 55649271 55649271 single base substitution C G upstream_gene_variant LUSC-KR 11 55649441 55649441 single base substitution C G upstream_gene_variant LUSC-KR 11 55649962 55649962 single base substitution G C upstream_gene_variant LUSC-KR 11 55650577 55650577 single base substitution C A upstream_gene_variant LUSC-KR 11 55650578 55650578 single base substitution G C upstream_gene_variant LUSC-KR 11 55651291 55651291 single base substitution C G intron_variant LUSC-KR 11 55651291 55651291 single base substitution C G upstream_gene_variant LUSC-KR 11 55651779 55651779 single base substitution T C intron_variant LUSC-KR 11 55651779 55651779 single base substitution T C upstream_gene_variant LUSC-KR 11 55652051 55652051 single base substitution A G intron_variant LUSC-KR 11 55652051 55652051 single base substitution A G upstream_gene_variant LUSC-KR 11 55653011 55653011 single base substitution G T missense_variant R36L 107G>T LUSC-KR 11 55653011 55653011 single base substitution G T upstream_gene_variant LUSC-KR 11 55654535 55654535 single base substitution T C intron_variant LUSC-KR 11 55654663 55654663 single base substitution C A intron_variant LUSC-KR 11 55654802 55654802 single base substitution C A intron_variant LUSC-KR 11 55655373 55655373 single base substitution G C intron_variant LUSC-KR 11 55656290 55656290 single base substitution G T intron_variant LUSC-KR 11 55656883 55656883 single base substitution A G intron_variant LUSC-KR 11 55657058 55657058 single base substitution C T intron_variant LUSC-KR 11 55657179 55657179 single base substitution C A intron_variant LUSC-KR 11 55658067 55658067 single base substitution G A intron_variant LUSC-KR 11 55658179 55658179 single base substitution G A intron_variant LUSC-KR 11 55658180 55658180 single base substitution G T intron_variant LUSC-KR 11 55660505 55660505 single base substitution C T downstream_gene_variant LUSC-KR 11 55661853 55661853 single base substitution G T downstream_gene_variant LUSC-KR 11 55661960 55661960 single base substitution C T downstream_gene_variant LUSC-KR 11 55661961 55661961 single base substitution C T downstream_gene_variant LUSC-KR 11 55662608 55662608 single base substitution A T downstream_gene_variant LUSC-KR 11 55662973 55662973 single base substitution C G downstream_gene_variant LUSC-KR 11 55663011 55663011 single base substitution G T downstream_gene_variant LUSC-KR 11 55664204 55664204 single base substitution C A downstream_gene_variant LUSC-US 11 55653687 55653687 single base substitution G T missense_variant C167F 500G>T LUSC-US 11 55653687 55653687 single base substitution G T missense_variant C24F 71G>T LUSC-US 11 55655539 55655539 single base substitution G T missense_variant R180I 539G>T LUSC-US 11 55655539 55655539 single base substitution G T missense_variant R37I 110G>T LUSC-US 11 55655543 55655543 single base substitution T A synonymous_variant A181A 543T>A LUSC-US 11 55655543 55655543 single base substitution T A synonymous_variant A38A 114T>A LUSC-US 11 55655595 55655595 single base substitution G C missense_variant E199Q 595G>C LUSC-US 11 55655595 55655595 single base substitution G C missense_variant E56Q 166G>C LUSC-US 11 55655637 55655637 single base substitution A G missense_variant N213D 637A>G LUSC-US 11 55655637 55655637 single base substitution A G missense_variant N70D 208A>G LUSC-US 11 55655725 55655725 single base substitution T A missense_variant V242E 725T>A LUSC-US 11 55655725 55655725 single base substitution T A missense_variant V99E 296T>A LUSC-US 11 55656477 55656477 single base substitution G T missense_variant R111M 332G>T LUSC-US 11 55656477 55656477 single base substitution G T missense_variant R254M 761G>T LUSC-US 11 55657463 55657463 single base substitution G T missense_variant E126D 378G>T LUSC-US 11 55657463 55657463 single base substitution G T missense_variant E269D 807G>T LUSC-US 11 55657498 55657498 single base substitution G A missense_variant S138N 413G>A LUSC-US 11 55657498 55657498 single base substitution G A missense_variant S281N 842G>A LUSC-US 11 55657502 55657502 single base substitution C A synonymous_variant L139L 417C>A LUSC-US 11 55657502 55657502 single base substitution C A synonymous_variant L282L 846C>A LUSC-US 11 55658796 55658796 single base substitution C A missense_variant D206E 618C>A LUSC-US 11 55658796 55658796 single base substitution C A missense_variant D349E 1047C>A LUSC-US 11 55658883 55658883 single base substitution T C synonymous_variant F235F 705T>C LUSC-US 11 55658883 55658883 single base substitution T C synonymous_variant F378F 1134T>C LUSC-US 11 55658946 55658946 single base substitution G A synonymous_variant V256V 768G>A LUSC-US 11 55658946 55658946 single base substitution G A synonymous_variant V399V 1197G>A MALY-DE 11 55645779 55645779 single base substitution G T upstream_gene_variant MALY-DE 11 55646225 55646225 single base substitution G A upstream_gene_variant MALY-DE 11 55648879 55648879 deletion of <=200bp A - upstream_gene_variant MALY-DE 11 55650747 55650747 single base substitution A G upstream_gene_variant MALY-DE 11 55653450 55653450 single base substitution C T 5_prime_UTR_variant MALY-DE 11 55653450 55653450 single base substitution C T intron_variant MALY-DE 11 55653451 55653451 single base substitution C T 5_prime_UTR_variant MALY-DE 11 55653451 55653451 single base substitution C T intron_variant MALY-DE 11 55653591 55653591 single base substitution T C 5_prime_UTR_variant MALY-DE 11 55653591 55653591 single base substitution T C splice_region_variant MALY-DE 11 55653610 55653610 deletion of <=200bp A - 5_prime_UTR_variant MALY-DE 11 55653610 55653610 deletion of <=200bp A - frameshift_variant L141 MALY-DE 11 55657756 55657756 single base substitution A C intron_variant MALY-DE 11 55658083 55658083 single base substitution G T intron_variant MELA-AU 11 55645831 55645831 single base substitution G A upstream_gene_variant MELA-AU 11 55645936 55645936 single base substitution C T upstream_gene_variant MELA-AU 11 55646015 55646015 single base substitution G A upstream_gene_variant MELA-AU 11 55646032 55646032 single base substitution A T upstream_gene_variant MELA-AU 11 55646048 55646048 single base substitution C T upstream_gene_variant MELA-AU 11 55646087 55646087 single base substitution C T upstream_gene_variant MELA-AU 11 55646150 55646150 single base substitution G A upstream_gene_variant MELA-AU 11 55646258 55646258 single base substitution C T upstream_gene_variant MELA-AU 11 55646418 55646418 single base substitution G A upstream_gene_variant MELA-AU 11 55646661 55646661 single base substitution A G upstream_gene_variant MELA-AU 11 55646664 55646664 single base substitution G A upstream_gene_variant MELA-AU 11 55646787 55646787 single base substitution G A upstream_gene_variant MELA-AU 11 55646846 55646846 single base substitution C T upstream_gene_variant MELA-AU 11 55646882 55646882 single base substitution G A upstream_gene_variant MELA-AU 11 55646915 55646915 single base substitution G A upstream_gene_variant MELA-AU 11 55646922 55646922 single base substitution C T upstream_gene_variant MELA-AU 11 55646923 55646923 single base substitution C T upstream_gene_variant MELA-AU 11 55646931 55646931 single base substitution G A upstream_gene_variant MELA-AU 11 55646945 55646945 single base substitution C T upstream_gene_variant MELA-AU 11 55646967 55646967 single base substitution G T upstream_gene_variant MELA-AU 11 55646975 55646975 single base substitution G A upstream_gene_variant MELA-AU 11 55647110 55647110 single base substitution G A upstream_gene_variant MELA-AU 11 55647137 55647137 single base substitution C T upstream_gene_variant MELA-AU 11 55647462 55647462 single base substitution C T upstream_gene_variant MELA-AU 11 55647564 55647564 single base substitution G A upstream_gene_variant MELA-AU 11 55647611 55647611 single base substitution C T upstream_gene_variant MELA-AU 11 55647857 55647857 single base substitution A T upstream_gene_variant MELA-AU 11 55648195 55648195 single base substitution C T upstream_gene_variant MELA-AU 11 55648392 55648392 single base substitution G A upstream_gene_variant MELA-AU 11 55648393 55648393 single base substitution G A upstream_gene_variant MELA-AU 11 55648490 55648490 single base substitution G A upstream_gene_variant MELA-AU 11 55648494 55648494 single base substitution C T upstream_gene_variant MELA-AU 11 55648695 55648695 single base substitution G A upstream_gene_variant MELA-AU 11 55648701 55648701 single base substitution C T upstream_gene_variant MELA-AU 11 55648735 55648735 single base substitution C T upstream_gene_variant MELA-AU 11 55648772 55648772 single base substitution C T upstream_gene_variant MELA-AU 11 55648776 55648776 single base substitution G A upstream_gene_variant MELA-AU 11 55648779 55648779 single base substitution G A upstream_gene_variant MELA-AU 11 55648784 55648784 single base substitution C T upstream_gene_variant MELA-AU 11 55648787 55648787 single base substitution C T upstream_gene_variant MELA-AU 11 55648800 55648800 single base substitution C T upstream_gene_variant MELA-AU 11 55648806 55648806 single base substitution G A upstream_gene_variant MELA-AU 11 55649064 55649064 single base substitution C T upstream_gene_variant MELA-AU 11 55649086 55649086 single base substitution G A upstream_gene_variant MELA-AU 11 55649109 55649109 single base substitution G A upstream_gene_variant MELA-AU 11 55649164 55649164 single base substitution C T upstream_gene_variant MELA-AU 11 55649181 55649181 single base substitution C T upstream_gene_variant MELA-AU 11 55649196 55649196 single base substitution A T upstream_gene_variant MELA-AU 11 55649411 55649411 single base substitution G A upstream_gene_variant MELA-AU 11 55649503 55649503 single base substitution C T upstream_gene_variant MELA-AU 11 55649513 55649513 single base substitution G A upstream_gene_variant MELA-AU 11 55649639 55649639 single base substitution C T upstream_gene_variant MELA-AU 11 55649782 55649782 single base substitution C T upstream_gene_variant MELA-AU 11 55649787 55649787 single base substitution G A upstream_gene_variant MELA-AU 11 55649839 55649839 single base substitution T C upstream_gene_variant MELA-AU 11 55649999 55649999 single base substitution G A upstream_gene_variant MELA-AU 11 55650244 55650244 single base substitution G A upstream_gene_variant MELA-AU 11 55650331 55650331 single base substitution C T upstream_gene_variant MELA-AU 11 55650417 55650417 single base substitution G A upstream_gene_variant MELA-AU 11 55650428 55650428 single base substitution C T upstream_gene_variant MELA-AU 11 55650596 55650596 single base substitution A G upstream_gene_variant MELA-AU 11 55650617 55650617 single base substitution C T upstream_gene_variant MELA-AU 11 55650787 55650787 single base substitution C T 5_prime_UTR_variant MELA-AU 11 55650787 55650787 single base substitution C T upstream_gene_variant MELA-AU 11 55650956 55650956 single base substitution G A intron_variant MELA-AU 11 55650956 55650956 single base substitution G A upstream_gene_variant MELA-AU 11 55651291 55651291 single base substitution C T intron_variant MELA-AU 11 55651291 55651291 single base substitution C T upstream_gene_variant MELA-AU 11 55651297 55651297 single base substitution G A intron_variant MELA-AU 11 55651297 55651297 single base substitution G A upstream_gene_variant MELA-AU 11 55651344 55651344 single base substitution G A intron_variant MELA-AU 11 55651344 55651344 single base substitution G A upstream_gene_variant MELA-AU 11 55651424 55651424 single base substitution G A intron_variant MELA-AU 11 55651424 55651424 single base substitution G A upstream_gene_variant MELA-AU 11 55651449 55651449 single base substitution G A intron_variant MELA-AU 11 55651449 55651449 single base substitution G A upstream_gene_variant MELA-AU 11 55651465 55651465 single base substitution G A intron_variant MELA-AU 11 55651465 55651465 single base substitution G A upstream_gene_variant MELA-AU 11 55651511 55651511 single base substitution C T intron_variant MELA-AU 11 55651511 55651511 single base substitution C T upstream_gene_variant MELA-AU 11 55651658 55651658 single base substitution T C intron_variant MELA-AU 11 55651658 55651658 single base substitution T C upstream_gene_variant MELA-AU 11 55651874 55651874 single base substitution C T intron_variant MELA-AU 11 55651874 55651874 single base substitution C T upstream_gene_variant MELA-AU 11 55651980 55651980 single base substitution G A intron_variant MELA-AU 11 55651980 55651980 single base substitution G A upstream_gene_variant MELA-AU 11 55652206 55652208 deletion of <=200bp ATA - intron_variant MELA-AU 11 55652206 55652208 deletion of <=200bp ATA - upstream_gene_variant MELA-AU 11 55652334 55652334 single base substitution C T intron_variant MELA-AU 11 55652334 55652334 single base substitution C T upstream_gene_variant MELA-AU 11 55652450 55652450 single base substitution G A intron_variant MELA-AU 11 55652450 55652450 single base substitution G A upstream_gene_variant MELA-AU 11 55652558 55652558 single base substitution G A intron_variant MELA-AU 11 55652558 55652558 single base substitution G A upstream_gene_variant MELA-AU 11 55652669 55652669 single base substitution G A intron_variant MELA-AU 11 55652669 55652669 single base substitution G A upstream_gene_variant MELA-AU 11 55652760 55652760 single base substitution C T intron_variant MELA-AU 11 55652760 55652760 single base substitution C T upstream_gene_variant MELA-AU 11 55652952 55652952 single base substitution C A synonymous_variant P16P 48C>A MELA-AU 11 55652952 55652952 single base substitution C A upstream_gene_variant MELA-AU 11 55653093 55653093 single base substitution C T synonymous_variant N63N 189C>T MELA-AU 11 55653093 55653093 single base substitution C T upstream_gene_variant MELA-AU 11 55653156 55653156 single base substitution A G synonymous_variant Q84Q 252A>G MELA-AU 11 55653156 55653156 single base substitution A G upstream_gene_variant MELA-AU 11 55653379 55653379 single base substitution C T intron_variant MELA-AU 11 55653379 55653379 single base substitution C T upstream_gene_variant MELA-AU 11 55653457 55653457 single base substitution G A 5_prime_UTR_variant MELA-AU 11 55653457 55653457 single base substitution G A intron_variant MELA-AU 11 55653474 55653474 single base substitution G A 5_prime_UTR_variant MELA-AU 11 55653474 55653474 single base substitution G A intron_variant MELA-AU 11 55653532 55653532 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 55653532 55653532 single base substitution C T intron_variant MELA-AU 11 55653635 55653635 single base substitution A T stop_gained K150* 448A>T MELA-AU 11 55653635 55653635 single base substitution A T stop_gained K7* 19A>T MELA-AU 11 55653690 55653690 single base substitution G A stop_gained W168* 503G>A MELA-AU 11 55653690 55653690 single base substitution G A stop_gained W25* 74G>A MELA-AU 11 55653807 55653807 single base substitution G A intron_variant MELA-AU 11 55653953 55653953 single base substitution G A intron_variant MELA-AU 11 55653977 55653977 single base substitution C T intron_variant MELA-AU 11 55653981 55653981 single base substitution A T intron_variant MELA-AU 11 55653983 55653983 single base substitution G A intron_variant MELA-AU 11 55654067 55654067 single base substitution G A intron_variant MELA-AU 11 55654096 55654096 single base substitution G A intron_variant MELA-AU 11 55654158 55654158 single base substitution G A intron_variant MELA-AU 11 55654267 55654267 single base substitution G A intron_variant MELA-AU 11 55654286 55654286 single base substitution G A intron_variant MELA-AU 11 55654357 55654357 single base substitution G A intron_variant MELA-AU 11 55654374 55654374 single base substitution C T intron_variant MELA-AU 11 55654700 55654700 single base substitution G A intron_variant MELA-AU 11 55654737 55654737 single base substitution C T intron_variant MELA-AU 11 55655020 55655020 single base substitution G A intron_variant MELA-AU 11 55655040 55655040 single base substitution A G intron_variant MELA-AU 11 55655202 55655202 single base substitution C T intron_variant MELA-AU 11 55655203 55655203 single base substitution G A intron_variant MELA-AU 11 55655211 55655211 single base substitution G A intron_variant MELA-AU 11 55655269 55655269 single base substitution C T intron_variant MELA-AU 11 55655372 55655372 single base substitution G A intron_variant MELA-AU 11 55655449 55655449 single base substitution C T intron_variant MELA-AU 11 55655453 55655453 single base substitution G A intron_variant MELA-AU 11 55655529 55655529 single base substitution G A missense_variant E177K 529G>A MELA-AU 11 55655529 55655529 single base substitution G A missense_variant E34K 100G>A MELA-AU 11 55655568 55655568 single base substitution C T missense_variant L190F 568C>T MELA-AU 11 55655568 55655568 single base substitution C T missense_variant L47F 139C>T MELA-AU 11 55655683 55655683 single base substitution G A missense_variant G228E 683G>A MELA-AU 11 55655683 55655683 single base substitution G A missense_variant G85E 254G>A MELA-AU 11 55655874 55655874 single base substitution G A intron_variant MELA-AU 11 55655915 55655915 single base substitution G A intron_variant MELA-AU 11 55655921 55655921 single base substitution C T intron_variant MELA-AU 11 55656016 55656016 single base substitution T A intron_variant MELA-AU 11 55656076 55656076 single base substitution G A intron_variant MELA-AU 11 55656114 55656114 single base substitution C T intron_variant MELA-AU 11 55656503 55656503 single base substitution G A intron_variant MELA-AU 11 55656517 55656517 single base substitution C T intron_variant MELA-AU 11 55656601 55656601 single base substitution C T intron_variant MELA-AU 11 55656728 55656728 single base substitution G A intron_variant MELA-AU 11 55656857 55656857 single base substitution G A intron_variant MELA-AU 11 55656964 55656965 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 11 55657077 55657077 single base substitution A C intron_variant MELA-AU 11 55657089 55657089 single base substitution C T intron_variant MELA-AU 11 55657124 55657124 single base substitution G A intron_variant MELA-AU 11 55657137 55657137 single base substitution C T intron_variant MELA-AU 11 55657377 55657377 single base substitution T G intron_variant MELA-AU 11 55657410 55657410 single base substitution C T splice_region_variant MELA-AU 11 55657513 55657513 single base substitution G A missense_variant R143K 428G>A MELA-AU 11 55657513 55657513 single base substitution G A missense_variant R286K 857G>A MELA-AU 11 55657655 55657655 single base substitution C T intron_variant MELA-AU 11 55657770 55657770 single base substitution G A intron_variant MELA-AU 11 55657861 55657861 single base substitution C T intron_variant MELA-AU 11 55657884 55657884 single base substitution C T intron_variant MELA-AU 11 55658106 55658106 single base substitution G A intron_variant MELA-AU 11 55658111 55658111 single base substitution C T intron_variant MELA-AU 11 55658131 55658131 single base substitution G A intron_variant MELA-AU 11 55658328 55658328 single base substitution C T intron_variant MELA-AU 11 55658440 55658440 single base substitution G A intron_variant MELA-AU 11 55658546 55658546 single base substitution C T intron_variant MELA-AU 11 55658701 55658701 single base substitution G A missense_variant D175N 523G>A MELA-AU 11 55658701 55658701 single base substitution G A missense_variant D318N 952G>A MELA-AU 11 55658707 55658707 single base substitution G A missense_variant D177N 529G>A MELA-AU 11 55658707 55658707 single base substitution G A missense_variant D320N 958G>A MELA-AU 11 55658717 55658717 single base substitution G A missense_variant G180E 539G>A MELA-AU 11 55658717 55658717 single base substitution G A missense_variant G323E 968G>A MELA-AU 11 55658723 55658723 single base substitution C T missense_variant S182F 545C>T MELA-AU 11 55658723 55658723 single base substitution C T missense_variant S325F 974C>T MELA-AU 11 55658846 55658846 single base substitution G A missense_variant R223K 668G>A MELA-AU 11 55658846 55658846 single base substitution G A missense_variant R366K 1097G>A MELA-AU 11 55659051 55659051 single base substitution C T synonymous_variant I291I 873C>T MELA-AU 11 55659051 55659051 single base substitution C T synonymous_variant I434I 1302C>T MELA-AU 11 55659062 55659062 single base substitution C T missense_variant S295F 884C>T MELA-AU 11 55659062 55659062 single base substitution C T missense_variant S438F 1313C>T MELA-AU 11 55659114 55659114 single base substitution G A 3_prime_UTR_variant MELA-AU 11 55659158 55659158 single base substitution C T 3_prime_UTR_variant MELA-AU 11 55659260 55659260 single base substitution C T 3_prime_UTR_variant MELA-AU 11 55659311 55659311 single base substitution A G downstream_gene_variant MELA-AU 11 55659434 55659434 single base substitution C T downstream_gene_variant MELA-AU 11 55659503 55659503 single base substitution G A downstream_gene_variant MELA-AU 11 55659563 55659563 single base substitution A G downstream_gene_variant MELA-AU 11 55659676 55659676 single base substitution T A downstream_gene_variant MELA-AU 11 55659740 55659740 single base substitution C T downstream_gene_variant MELA-AU 11 55659799 55659799 single base substitution G A downstream_gene_variant MELA-AU 11 55659853 55659853 single base substitution G A downstream_gene_variant MELA-AU 11 55660071 55660071 single base substitution C T downstream_gene_variant MELA-AU 11 55660107 55660107 deletion of <=200bp A - downstream_gene_variant MELA-AU 11 55660448 55660448 single base substitution T C downstream_gene_variant MELA-AU 11 55660506 55660506 single base substitution G A downstream_gene_variant MELA-AU 11 55660641 55660641 single base substitution A T downstream_gene_variant MELA-AU 11 55661036 55661036 single base substitution C T downstream_gene_variant MELA-AU 11 55661045 55661045 single base substitution C T downstream_gene_variant MELA-AU 11 55661339 55661339 single base substitution C T downstream_gene_variant MELA-AU 11 55661341 55661341 single base substitution C T downstream_gene_variant MELA-AU 11 55661432 55661432 single base substitution G A downstream_gene_variant MELA-AU 11 55661438 55661438 single base substitution G A downstream_gene_variant MELA-AU 11 55661448 55661448 single base substitution G A downstream_gene_variant MELA-AU 11 55661494 55661494 single base substitution G A downstream_gene_variant MELA-AU 11 55661527 55661527 single base substitution C T downstream_gene_variant MELA-AU 11 55661607 55661607 single base substitution C T downstream_gene_variant MELA-AU 11 55661641 55661641 single base substitution C T downstream_gene_variant MELA-AU 11 55661656 55661656 single base substitution G A downstream_gene_variant MELA-AU 11 55661751 55661751 single base substitution G A downstream_gene_variant MELA-AU 11 55661866 55661866 single base substitution G T downstream_gene_variant MELA-AU 11 55661902 55661902 single base substitution C T downstream_gene_variant MELA-AU 11 55661936 55661936 single base substitution G A downstream_gene_variant MELA-AU 11 55661948 55661948 single base substitution G A downstream_gene_variant MELA-AU 11 55661957 55661957 single base substitution G A downstream_gene_variant MELA-AU 11 55662009 55662009 single base substitution C T downstream_gene_variant MELA-AU 11 55662117 55662117 single base substitution G A downstream_gene_variant MELA-AU 11 55662232 55662232 single base substitution G A downstream_gene_variant MELA-AU 11 55662233 55662233 single base substitution G A downstream_gene_variant MELA-AU 11 55662237 55662237 single base substitution G A downstream_gene_variant MELA-AU 11 55662304 55662304 single base substitution G A downstream_gene_variant MELA-AU 11 55662366 55662366 single base substitution C T downstream_gene_variant MELA-AU 11 55662423 55662423 single base substitution C T downstream_gene_variant MELA-AU 11 55662434 55662434 single base substitution C T downstream_gene_variant MELA-AU 11 55662490 55662490 single base substitution G A downstream_gene_variant MELA-AU 11 55662535 55662535 single base substitution C T downstream_gene_variant MELA-AU 11 55662540 55662540 single base substitution A C downstream_gene_variant MELA-AU 11 55662580 55662580 single base substitution G A downstream_gene_variant MELA-AU 11 55662688 55662688 single base substitution G A downstream_gene_variant MELA-AU 11 55662697 55662697 single base substitution C T downstream_gene_variant MELA-AU 11 55662853 55662853 single base substitution C T downstream_gene_variant MELA-AU 11 55662869 55662869 single base substitution G A downstream_gene_variant MELA-AU 11 55662888 55662888 single base substitution C T downstream_gene_variant MELA-AU 11 55662939 55662939 single base substitution C T downstream_gene_variant MELA-AU 11 55662951 55662951 single base substitution C T downstream_gene_variant MELA-AU 11 55663004 55663004 single base substitution G A downstream_gene_variant MELA-AU 11 55663016 55663016 single base substitution G A downstream_gene_variant MELA-AU 11 55663115 55663115 single base substitution C A downstream_gene_variant MELA-AU 11 55663118 55663118 single base substitution C T downstream_gene_variant MELA-AU 11 55663349 55663349 single base substitution C T downstream_gene_variant MELA-AU 11 55663414 55663414 single base substitution C T downstream_gene_variant MELA-AU 11 55663753 55663753 single base substitution G A downstream_gene_variant MELA-AU 11 55663784 55663784 single base substitution G A downstream_gene_variant MELA-AU 11 55663813 55663813 single base substitution C T downstream_gene_variant MELA-AU 11 55664100 55664100 single base substitution G A downstream_gene_variant MELA-AU 11 55664126 55664126 single base substitution G T downstream_gene_variant ORCA-IN 11 55647078 55647078 single base substitution C T upstream_gene_variant ORCA-IN 11 55651558 55651558 single base substitution A G intron_variant ORCA-IN 11 55651558 55651558 single base substitution A G upstream_gene_variant ORCA-IN 11 55653269 55653269 single base substitution G A missense_variant R122Q 365G>A ORCA-IN 11 55653269 55653269 single base substitution G A upstream_gene_variant OV-AU 11 55646770 55646770 single base substitution A G upstream_gene_variant OV-AU 11 55647489 55647489 single base substitution G A upstream_gene_variant OV-AU 11 55647581 55647581 single base substitution A T upstream_gene_variant OV-AU 11 55650515 55650515 single base substitution C A upstream_gene_variant OV-AU 11 55650949 55650949 single base substitution A T intron_variant OV-AU 11 55650949 55650949 single base substitution A T upstream_gene_variant OV-AU 11 55651745 55651745 single base substitution G C intron_variant OV-AU 11 55651745 55651745 single base substitution G C upstream_gene_variant OV-AU 11 55655929 55655929 single base substitution C T intron_variant OV-AU 11 55658225 55658225 single base substitution C A intron_variant OV-AU 11 55660244 55660244 single base substitution T A downstream_gene_variant OV-AU 11 55660390 55660390 single base substitution G A downstream_gene_variant OV-AU 11 55662253 55662253 single base substitution T A downstream_gene_variant OV-US 11 55653305 55653305 single base substitution A T missense_variant E134V 401A>T OV-US 11 55653305 55653305 single base substitution A T upstream_gene_variant PACA-AU 11 55646174 55646174 single base substitution T C upstream_gene_variant PACA-AU 11 55646327 55646327 single base substitution C T upstream_gene_variant PACA-AU 11 55647505 55647505 single base substitution G T upstream_gene_variant PACA-AU 11 55649117 55649117 single base substitution T A upstream_gene_variant PACA-AU 11 55649826 55649826 single base substitution G A upstream_gene_variant PACA-AU 11 55649881 55649881 single base substitution A G upstream_gene_variant PACA-AU 11 55650820 55650820 single base substitution C A 5_prime_UTR_variant PACA-AU 11 55650820 55650820 single base substitution C A upstream_gene_variant PACA-AU 11 55652634 55652634 single base substitution G A intron_variant PACA-AU 11 55652634 55652634 single base substitution G A upstream_gene_variant PACA-AU 11 55652915 55652915 single base substitution G T missense_variant G4V 11G>T PACA-AU 11 55652915 55652915 single base substitution G T upstream_gene_variant PACA-AU 11 55652965 55652965 single base substitution T C missense_variant Y21H 61T>C PACA-AU 11 55652965 55652965 single base substitution T C upstream_gene_variant PACA-AU 11 55654011 55654011 single base substitution G T intron_variant PACA-AU 11 55654322 55654322 single base substitution G A intron_variant PACA-AU 11 55654480 55654480 single base substitution C A intron_variant PACA-AU 11 55656487 55656487 single base substitution C T intron_variant PACA-AU 11 55656861 55656861 single base substitution A G intron_variant PACA-AU 11 55657236 55657236 single base substitution C T intron_variant PACA-AU 11 55657256 55657256 single base substitution G A intron_variant PACA-AU 11 55658461 55658461 single base substitution T A intron_variant PACA-AU 11 55658484 55658484 single base substitution T A intron_variant PACA-AU 11 55661316 55661316 single base substitution G A downstream_gene_variant PACA-AU 11 55663389 55663389 single base substitution C T downstream_gene_variant PACA-CA 11 55646058 55646058 single base substitution T A upstream_gene_variant PACA-CA 11 55646486 55646486 single base substitution A C upstream_gene_variant PACA-CA 11 55646786 55646786 single base substitution G A upstream_gene_variant PACA-CA 11 55647093 55647093 single base substitution C T upstream_gene_variant PACA-CA 11 55647332 55647332 single base substitution T G upstream_gene_variant PACA-CA 11 55647518 55647518 single base substitution T A upstream_gene_variant PACA-CA 11 55648169 55648169 single base substitution C T upstream_gene_variant PACA-CA 11 55649585 55649585 single base substitution T C upstream_gene_variant PACA-CA 11 55650577 55650577 single base substitution C T upstream_gene_variant PACA-CA 11 55652403 55652403 single base substitution G A intron_variant PACA-CA 11 55652403 55652403 single base substitution G A upstream_gene_variant PACA-CA 11 55653245 55653245 single base substitution C T missense_variant P114L 341C>T PACA-CA 11 55653245 55653245 single base substitution C T upstream_gene_variant PACA-CA 11 55653269 55653269 single base substitution G A missense_variant R122Q 365G>A PACA-CA 11 55653269 55653269 single base substitution G A upstream_gene_variant PACA-CA 11 55653610 55653610 deletion of <=200bp A - 5_prime_UTR_variant PACA-CA 11 55653610 55653610 deletion of <=200bp A - frameshift_variant L141 PACA-CA 11 55654146 55654146 single base substitution A G intron_variant PACA-CA 11 55654330 55654330 single base substitution C G intron_variant PACA-CA 11 55655018 55655018 single base substitution C T intron_variant PACA-CA 11 55655020 55655020 single base substitution G T intron_variant PACA-CA 11 55655605 55655605 single base substitution G A missense_variant R202Q 605G>A PACA-CA 11 55655605 55655605 single base substitution G A missense_variant R59Q 176G>A PACA-CA 11 55657059 55657059 single base substitution G A intron_variant PACA-CA 11 55657196 55657196 single base substitution G A intron_variant PACA-CA 11 55657373 55657373 deletion of <=200bp T - intron_variant PACA-CA 11 55657795 55657795 single base substitution A C intron_variant PACA-CA 11 55658011 55658011 single base substitution A T intron_variant PACA-CA 11 55658082 55658082 single base substitution C T intron_variant PACA-CA 11 55658725 55658725 single base substitution G A missense_variant E183K 547G>A PACA-CA 11 55658725 55658725 single base substitution G A missense_variant E326K 976G>A PACA-CA 11 55660689 55660689 single base substitution G A downstream_gene_variant PACA-CA 11 55661249 55661249 single base substitution G A downstream_gene_variant PACA-CA 11 55661690 55661690 single base substitution C G downstream_gene_variant PACA-CA 11 55662123 55662123 single base substitution C T downstream_gene_variant PACA-CA 11 55662193 55662193 single base substitution G T downstream_gene_variant PACA-CA 11 55662321 55662321 single base substitution C T downstream_gene_variant PACA-CA 11 55664087 55664087 single base substitution T A downstream_gene_variant PAEN-AU 11 55650486 55650490 deletion of <=200bp TACTC - upstream_gene_variant PAEN-AU 11 55651713 55651713 single base substitution A G intron_variant PAEN-AU 11 55651713 55651713 single base substitution A G upstream_gene_variant PAEN-AU 11 55655638 55655638 single base substitution A G missense_variant N213S 638A>G PAEN-AU 11 55655638 55655638 single base substitution A G missense_variant N70S 209A>G PAEN-AU 11 55660220 55660220 single base substitution G A downstream_gene_variant PBCA-DE 11 55648970 55648970 insertion of <=200bp - G upstream_gene_variant PBCA-DE 11 55653629 55653629 single base substitution T A missense_variant W148R 442T>A PBCA-DE 11 55653629 55653629 single base substitution T A missense_variant W5R 13T>A PBCA-DE 11 55654778 55654779 deletion of <=200bp TA - intron_variant PBCA-DE 11 55656477 55656477 single base substitution G T missense_variant R111M 332G>T PBCA-DE 11 55656477 55656477 single base substitution G T missense_variant R254M 761G>T PBCA-DE 11 55657373 55657373 insertion of <=200bp - T intron_variant PRAD-CA 11 55649707 55649707 single base substitution G A upstream_gene_variant PRAD-CA 11 55655615 55655615 single base substitution C A synonymous_variant G205G 615C>A PRAD-CA 11 55655615 55655615 single base substitution C A synonymous_variant G62G 186C>A PRAD-CA 11 55656467 55656467 single base substitution A G missense_variant I108V 322A>G PRAD-CA 11 55656467 55656467 single base substitution A G missense_variant I251V 751A>G PRAD-CA 11 55660420 55660420 single base substitution C T downstream_gene_variant PRAD-CA 11 55662728 55662728 single base substitution C T downstream_gene_variant PRAD-UK 11 55646165 55646178 multiple base substitution (>=2bp and <=200bp) TCTTTCAGTTTCCA TTGATATT upstream_gene_variant PRAD-UK 11 55649962 55649962 single base substitution G A upstream_gene_variant PRAD-UK 11 55651798 55651798 single base substitution C T intron_variant PRAD-UK 11 55651798 55651798 single base substitution C T upstream_gene_variant PRAD-UK 11 55652011 55652011 single base substitution C G intron_variant PRAD-UK 11 55652011 55652011 single base substitution C G upstream_gene_variant PRAD-UK 11 55652031 55652031 single base substitution C G intron_variant PRAD-UK 11 55652031 55652031 single base substitution C G upstream_gene_variant PRAD-UK 11 55652058 55652058 single base substitution C G intron_variant PRAD-UK 11 55652058 55652058 single base substitution C G upstream_gene_variant PRAD-UK 11 55652188 55652188 single base substitution C T intron_variant PRAD-UK 11 55652188 55652188 single base substitution C T upstream_gene_variant PRAD-UK 11 55654959 55654959 single base substitution A T intron_variant PRAD-UK 11 55655020 55655020 single base substitution G A intron_variant PRAD-UK 11 55659492 55659492 single base substitution G A downstream_gene_variant PRAD-UK 11 55660378 55660378 single base substitution T A downstream_gene_variant PRAD-UK 11 55661934 55661934 single base substitution A G downstream_gene_variant RECA-EU 11 55646640 55646640 single base substitution C T upstream_gene_variant RECA-EU 11 55646931 55646931 single base substitution G A upstream_gene_variant RECA-EU 11 55648940 55648940 single base substitution C A upstream_gene_variant RECA-EU 11 55649191 55649191 single base substitution A G upstream_gene_variant RECA-EU 11 55657807 55657807 single base substitution G A intron_variant RECA-EU 11 55661518 55661518 single base substitution T A downstream_gene_variant RECA-EU 11 55662207 55662207 single base substitution A T downstream_gene_variant RECA-EU 11 55662908 55662908 single base substitution T A downstream_gene_variant SKCA-BR 11 55645806 55645806 single base substitution C T upstream_gene_variant SKCA-BR 11 55647105 55647105 single base substitution G A upstream_gene_variant SKCA-BR 11 55648274 55648274 single base substitution G A upstream_gene_variant SKCA-BR 11 55649004 55649004 single base substitution G A upstream_gene_variant SKCA-BR 11 55649181 55649181 single base substitution C T upstream_gene_variant SKCA-BR 11 55649795 55649795 single base substitution T C upstream_gene_variant SKCA-BR 11 55649867 55649867 single base substitution G A upstream_gene_variant SKCA-BR 11 55651658 55651658 insertion of <=200bp - TATAC intron_variant SKCA-BR 11 55651658 55651658 insertion of <=200bp - TATAC upstream_gene_variant SKCA-BR 11 55653379 55653379 single base substitution C T intron_variant SKCA-BR 11 55653379 55653379 single base substitution C T upstream_gene_variant SKCA-BR 11 55653394 55653394 single base substitution G A intron_variant SKCA-BR 11 55653394 55653394 single base substitution G A upstream_gene_variant SKCA-BR 11 55653471 55653471 single base substitution G A 5_prime_UTR_variant SKCA-BR 11 55653471 55653471 single base substitution G A intron_variant SKCA-BR 11 55653768 55653768 single base substitution G A intron_variant SKCA-BR 11 55654858 55654858 single base substitution T A intron_variant SKCA-BR 11 55655382 55655382 single base substitution T A intron_variant SKCA-BR 11 55655508 55655508 single base substitution G A missense_variant D170N 508G>A SKCA-BR 11 55655508 55655508 single base substitution G A missense_variant D27N 79G>A SKCA-BR 11 55656517 55656517 single base substitution C T intron_variant SKCA-BR 11 55656534 55656534 single base substitution G A intron_variant SKCA-BR 11 55657153 55657153 single base substitution C T intron_variant SKCA-BR 11 55657609 55657609 single base substitution C T intron_variant SKCA-BR 11 55661306 55661306 single base substitution C T downstream_gene_variant SKCA-BR 11 55661528 55661528 single base substitution C T downstream_gene_variant SKCA-BR 11 55661688 55661688 single base substitution C T downstream_gene_variant SKCA-BR 11 55661727 55661727 single base substitution A G downstream_gene_variant SKCA-BR 11 55664168 55664168 single base substitution G A downstream_gene_variant SKCM-US 11 55652907 55652907 single base substitution G A start_lost M1I 3G>A SKCM-US 11 55652907 55652907 single base substitution G A upstream_gene_variant SKCM-US 11 55652961 55652961 single base substitution G A missense_variant M19I 57G>A SKCM-US 11 55652961 55652961 single base substitution G A upstream_gene_variant SKCM-US 11 55652968 55652968 single base substitution T C missense_variant F22L 64T>C SKCM-US 11 55652968 55652968 single base substitution T C upstream_gene_variant SKCM-US 11 55652970 55652970 single base substitution C T synonymous_variant F22F 66C>T SKCM-US 11 55652970 55652970 single base substitution C T upstream_gene_variant SKCM-US 11 55653012 55653012 single base substitution G A synonymous_variant R36R 108G>A SKCM-US 11 55653012 55653012 single base substitution G A upstream_gene_variant SKCM-US 11 55653172 55653172 single base substitution G A missense_variant E90K 268G>A SKCM-US 11 55653172 55653172 single base substitution G A upstream_gene_variant SKCM-US 11 55653186 55653186 single base substitution G A synonymous_variant G94G 282G>A SKCM-US 11 55653186 55653186 single base substitution G A upstream_gene_variant SKCM-US 11 55653197 55653197 single base substitution A T missense_variant E98V 293A>T SKCM-US 11 55653197 55653197 single base substitution A T upstream_gene_variant SKCM-US 11 55653274 55653274 single base substitution C T missense_variant H124Y 370C>T SKCM-US 11 55653274 55653274 single base substitution C T upstream_gene_variant SKCM-US 11 55653307 55653307 single base substitution G A missense_variant E135K 403G>A SKCM-US 11 55653307 55653307 single base substitution G A upstream_gene_variant SKCM-US 11 55653314 55653314 single base substitution G A missense_variant R137Q 410G>A SKCM-US 11 55653314 55653314 single base substitution G A upstream_gene_variant SKCM-US 11 55653632 55653632 single base substitution G A missense_variant E149K 445G>A SKCM-US 11 55653632 55653632 single base substitution G A missense_variant E6K 16G>A SKCM-US 11 55655529 55655529 single base substitution G A missense_variant E177K 529G>A SKCM-US 11 55655529 55655529 single base substitution G A missense_variant E34K 100G>A SKCM-US 11 55655574 55655574 single base substitution G A missense_variant E192K 574G>A SKCM-US 11 55655574 55655574 single base substitution G A missense_variant E49K 145G>A SKCM-US 11 55655577 55655577 single base substitution G A missense_variant E193K 577G>A SKCM-US 11 55655577 55655577 single base substitution G A missense_variant E50K 148G>A SKCM-US 11 55655605 55655605 single base substitution G A missense_variant R202Q 605G>A SKCM-US 11 55655605 55655605 single base substitution G A missense_variant R59Q 176G>A SKCM-US 11 55655610 55655610 single base substitution G A missense_variant E204K 610G>A SKCM-US 11 55655610 55655610 single base substitution G A missense_variant E61K 181G>A SKCM-US 11 55655644 55655644 single base substitution G A missense_variant S215N 644G>A SKCM-US 11 55655644 55655644 single base substitution G A missense_variant S72N 215G>A SKCM-US 11 55658717 55658717 single base substitution G A missense_variant G180E 539G>A SKCM-US 11 55658717 55658717 single base substitution G A missense_variant G323E 968G>A SKCM-US 11 55658779 55658779 single base substitution G A missense_variant E201K 601G>A SKCM-US 11 55658779 55658779 single base substitution G A missense_variant E344K 1030G>A SKCM-US 11 55658834 55658834 single base substitution G A stop_gained W219* 656G>A SKCM-US 11 55658834 55658834 single base substitution G A stop_gained W362* 1085G>A SKCM-US 11 55659052 55659052 single base substitution C T missense_variant P292S 874C>T SKCM-US 11 55659052 55659052 single base substitution C T missense_variant P435S 1303C>T STAD-US 11 55653074 55653074 single base substitution A C missense_variant K57T 170A>C STAD-US 11 55653074 55653074 single base substitution A C upstream_gene_variant STAD-US 11 55653152 55653152 single base substitution G T missense_variant R83L 248G>T STAD-US 11 55653152 55653152 single base substitution G T upstream_gene_variant STAD-US 11 55653609 55653609 insertion of <=200bp - A 5_prime_UTR_variant STAD-US 11 55653609 55653609 insertion of <=200bp - A frameshift_variant L141H? STAD-US 11 55656478 55656478 single base substitution G C splice_donor_variant STAD-US 11 55657447 55657447 single base substitution A T missense_variant E121V 362A>T STAD-US 11 55657447 55657447 single base substitution A T missense_variant E264V 791A>T STAD-US 11 55658701 55658701 single base substitution G T missense_variant D175Y 523G>T STAD-US 11 55658701 55658701 single base substitution G T missense_variant D318Y 952G>T STAD-US 11 55658772 55658772 single base substitution T C synonymous_variant Y198Y 594T>C STAD-US 11 55658772 55658772 single base substitution T C synonymous_variant Y341Y 1023T>C STAD-US 11 55659067 55659067 single base substitution T C missense_variant S297P 889T>C STAD-US 11 55659067 55659067 single base substitution T C missense_variant S440P 1318T>C STAD-US 11 55659079 55659079 single base substitution A G missense_variant R301G 901A>G STAD-US 11 55659079 55659079 single base substitution A G missense_variant R444G 1330A>G THCA-US 11 55658652 55658652 single base substitution C G missense_variant F158L 474C>G THCA-US 11 55658652 55658652 single base substitution C G missense_variant F301L 903C>G THCA-US 11 55659057 55659057 single base substitution T C synonymous_variant N293N 879T>C THCA-US 11 55659057 55659057 single base substitution T C synonymous_variant N436N 1308T>C UCEC-US 11 55652996 55652996 single base substitution G T missense_variant G31V 92G>T UCEC-US 11 55652996 55652996 single base substitution G T upstream_gene_variant UCEC-US 11 55653041 55653041 single base substitution C T missense_variant T46M 137C>T UCEC-US 11 55653041 55653041 single base substitution C T upstream_gene_variant UCEC-US 11 55653066 55653066 single base substitution A C missense_variant E54D 162A>C UCEC-US 11 55653066 55653066 single base substitution A C upstream_gene_variant UCEC-US 11 55653080 55653080 single base substitution C T missense_variant T59M 176C>T UCEC-US 11 55653080 55653080 single base substitution C T upstream_gene_variant UCEC-US 11 55653151 55653151 single base substitution C T missense_variant R83W 247C>T UCEC-US 11 55653151 55653151 single base substitution C T upstream_gene_variant UCEC-US 11 55653246 55653246 single base substitution G A synonymous_variant P114P 342G>A UCEC-US 11 55653246 55653246 single base substitution G A upstream_gene_variant UCEC-US 11 55653264 55653264 single base substitution G T missense_variant E120D 360G>T UCEC-US 11 55653264 55653264 single base substitution G T upstream_gene_variant UCEC-US 11 55655656 55655656 single base substitution T C missense_variant M219T 656T>C UCEC-US 11 55655656 55655656 single base substitution T C missense_variant M76T 227T>C UCEC-US 11 55655739 55655739 single base substitution G T splice_donor_variant UCEC-US 11 55658887 55658887 single base substitution C A missense_variant L237I 709C>A UCEC-US 11 55658887 55658887 single base substitution C A missense_variant L380I 1138C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand C086 COSM4807199 c.499G>A p.E167K Substitution - Missense 11:55891249-55891249 + XHDG37 COSM4195072 c.284+2T>G p.? Unknown 11:55889003-55889003 + LUAD-B01102 COSM333151 c.805A>C p.S269R Substitution - Missense 11:55891555-55891555 + 6115237 COSM4033725 c.475G>T p.D159Y Substitution - Missense 11:55891225-55891225 + TCGA-60-2698-01 COSM688792 c.118G>C p.E40Q Substitution - Missense 11:55888119-55888119 + DU-145 COSM1676001 c.27G>T p.W9C Substitution - Missense 11:55886215-55886215 + TCGA-AA-3715-01 COSM270234 c.213T>G p.Y71* Substitution - Nonsense 11:55888214-55888214 + 292_T COSM3953315 c.182A>G p.E61G Substitution - Missense 11:55888183-55888183 + TCGA-EE-A20F-06 COSM3449087 c.167G>A p.S56N Substitution - Missense 11:55888168-55888168 + LUAD-RT-S01813 COSM383053 c.852C>A p.L284L Substitution - coding silent 11:55891602-55891602 + TCGA-60-2713-01 COSM688788 c.248T>A p.V83E Substitution - Missense 11:55888249-55888249 + 522_T COSM3953317 c.407G>T p.R136I Substitution - Missense 11:55891157-55891157 + TCGA-22-1016-01 COSM688790 c.160A>G p.N54D Substitution - Missense 11:55888161-55888161 + CSCC-54-T COSM4555507 c.180G>A p.M60I Substitution - Missense 11:55888181-55888181 + TCGA-16-0846-01 COSM326561 c.114C>A p.H38Q Substitution - Missense 11:55888115-55888115 + TCGA-85-6175-01 COSM688798 c.23G>T p.C8F Substitution - Missense 11:55886211-55886211 + LUAD-YINHD COSM348448 c.758T>A p.F253Y Substitution - Missense 11:55891508-55891508 + PCSI_0467_Pa_P_526 COSM4807199 c.499G>A p.E167K Substitution - Missense 11:55891249-55891249 + TCGA-D5-6531-01 COSM3687378 c.260A>T p.Q87L Substitution - Missense 11:55888261-55888261 + PT37 COSM5920302 c.268G>A p.G90R Substitution - Missense 11:55888985-55888985 + LUAD-NYU408 COSM374036 c.346A>G p.I116V Substitution - Missense 11:55890003-55890003 + TCGA-46-3767-01 COSM688794 c.66T>A p.A22A Substitution - coding silent 11:55888067-55888067 + ESCC_143 COSM5643975 c.244G>A p.D82N Substitution - Missense 11:55888245-55888245 + LUAD-5V8LT COSM401189 c.621A>G p.R207R Substitution - coding silent 11:55891371-55891371 + LUAD-CHTN-MAD06-00668 COSM358539 c.24C>A p.C8* Substitution - Nonsense 11:55886212-55886212 + T2940 COSM4736143 c.94C>T p.H32Y Substitution - Missense 11:55888095-55888095 + CN-AML-36-T COSM4195072 c.284+2T>G p.? Unknown 11:55889003-55889003 + 8051723 COSM4135683 c.161A>G p.N54S Substitution - Missense 11:55888162-55888162 + 8016470 COSM3769343 c.284+10C>T p.? Unknown 11:55889011-55889011 + TCGA-33-4532-01 COSM688776 c.570C>A p.D190E Substitution - Missense 11:55891320-55891320 + TCGA-06-0168-01 COSM3397807 c.688T>A p.C230S Substitution - Missense 11:55891438-55891438 + TCGA-BH-A0HP-01 COSM429180 c.27G>A p.W9* Substitution - Nonsense 11:55886215-55886215 + TCGA-FS-A4F9-06 COSM3449085 c.128G>A p.R43Q Substitution - Missense 11:55888129-55888129 + YUNIBO COSM1703944 c.374G>A p.G125E Substitution - Missense 11:55890031-55890031 + TCGA-G2-A2EF-01 COSM1298148 c.463G>C p.D155H Substitution - Missense 11:55891213-55891213 + TCGA-BR-4257-01 COSM4033731 c.853A>G p.R285G Substitution - Missense 11:55891603-55891603 + TCGA-BR-8485-01 COSM4033729 c.841T>C p.S281P Substitution - Missense 11:55891591-55891591 + 422_T COSM3953319 c.690C>A p.C230* Substitution - Nonsense 11:55891440-55891440 + TCGA-FW-A3R5-06 COSM3869416 c.553G>A p.E185K Substitution - Missense 11:55891303-55891303 + TCGA-AX-A0IU-01 COSM928140 c.122G>C p.R41T Substitution - Missense 11:55888123-55888123 + TCGA-AY-6386-01 COSM1354506 c.109C>T p.H37Y Substitution - Missense 11:55888110-55888110 + LP6005334-DNA_E01 COSM4412566 c.480C>A p.P160P Substitution - coding silent 11:55891230-55891230 + PT36 COSM5916131 c.649G>A p.G217R Substitution - Missense 11:55891399-55891399 + CN-AML-NR-36-Dx COSM4195072 c.284+2T>G p.? Unknown 11:55889003-55889003 + TCGA-BS-A0UV-01 COSM928142 c.179T>C p.M60T Substitution - Missense 11:55888180-55888180 + C086 COSM5539677 c.763G>A p.D255N Substitution - Missense 11:55891513-55891513 + LUAD-CHTN-MAD08-00104 COSM361123 c.630C>A p.D210E Substitution - Missense 11:55891380-55891380 + Patient_4_Diagnosis COSM4195072 c.284+2T>G p.? Unknown 11:55889003-55889003 + CSCC-41-T COSM4555850 c.193G>A p.E65K Substitution - Missense 11:55888194-55888194 + PT37 COSM4195099 c.481G>A p.D161N Substitution - Missense 11:55891231-55891231 + TCGA-AA-3819-01 COSM294059 c.607T>C p.W203R Substitution - Missense 11:55891357-55891357 + TCGA-18-3417-01 COSM688782 c.365G>A p.S122N Substitution - Missense 11:55890022-55890022 + T578 COSM4736145 c.867C>A p.C289* Substitution - Nonsense 11:55891617-55891617 + YUKLAB COSM1703946 c.769G>A p.E257K Substitution - Missense 11:55891519-55891519 + B85-2-Tumor COSM1746317 c.539G>T p.G180V Substitution - Missense 11:55891289-55891289 + PD10011a COSM5798021 c.518G>C p.G173A Substitution - Missense 11:55891268-55891268 + TCGA-29-1761-01 COSM1321628 c.112C>T p.H38Y Substitution - Missense 11:55888113-55888113 + TCGA-G3-A25V-01 COSM4914524 c.289G>A p.E97K Substitution - Missense 11:55889946-55889946 + TCGA-GD-A3OQ-01 COSM1298150 c.559C>T p.H187Y Substitution - Missense 11:55891309-55891309 + BRC37 COSM5027391 c.503G>T p.C168F Substitution - Missense 11:55891253-55891253 + TCGA-G3-A5SL-01 COSM4929686 c.796G>A p.V266I Substitution - Missense 11:55891546-55891546 + ESO-085 COSM1266693 c.215A>T p.E72V Substitution - Missense 11:55888216-55888216 + CSCC-55-T COSM4552211 c.75G>A p.Q25Q Substitution - coding silent 11:55888076-55888076 + LUAD-E00443 COSM363647 c.608G>A p.W203* Substitution - Nonsense 11:55891358-55891358 + TCGA-F4-6570-01 COSM1354510 c.317C>A p.P106H Substitution - Missense 11:55889974-55889974 + PCSI_0341_Pa_P_526 COSM3449085 c.128G>A p.R43Q Substitution - Missense 11:55888129-55888129 + TCGA-18-5592-01 COSM215472 c.284G>T p.R95M Substitution - Missense 11:55889001-55889001 + pfg029T COSM401189 c.621A>G p.R207R Substitution - coding silent 11:55891371-55891371 + TCGA-A8-A09Q-01 COSM429184 c.643G>A p.E215K Substitution - Missense 11:55891393-55891393 + YUNIBO COSM5372729 c.357G>A p.L119L Substitution - coding silent 11:55890014-55890014 + TCGA-DW-7839-01 COSM3986236 c.548A>G p.Y183C Substitution - Missense 11:55891298-55891298 + TCGA-BR-6453-01 COSM4033722 c.314A>T p.E105V Substitution - Missense 11:55889971-55889971 + ZZUFHECRKL-G056T COSM5438104 c.688T>C p.C230R Substitution - Missense 11:55891438-55891438 + S00841 COSM5661809 c.453T>C p.N151N Substitution - coding silent 11:55891203-55891203 + TCGA-66-2759-01 COSM688784 c.330G>T p.E110D Substitution - Missense 11:55889987-55889987 + TCGA-56-1622-01 COSM688796 c.62G>T p.R21I Substitution - Missense 11:55888063-55888063 + TCGA-L6-A4EU-01 COSM3368409 c.426C>G p.F142L Substitution - Missense 11:55891176-55891176 + B85-2 COSM1746317 c.539G>T p.G180V Substitution - Missense 11:55891289-55891289 + C086 COSM5539679 c.508C>T p.L170F Substitution - Missense 11:55891258-55891258 + S00941 COSM5663617 c.9C>A p.T3T Substitution - coding silent 11:55886197-55886197 + TCGA-EK-A2PM-01 COSM4831542 c.403G>A p.E135K Substitution - Missense 11:55891153-55891153 + TCGA-A6-5659-01 COSM1354512 c.780C>A p.T260T Substitution - coding silent 11:55891530-55891530 + TCGA-CW-6093-01 COSM466942 c.463G>T p.D155Y Substitution - Missense 11:55891213-55891213 + ESO-0280 COSM1266691 c.197T>A p.L66H Substitution - Missense 11:55888198-55888198 + PT35 COSM4195099 c.481G>A p.D161N Substitution - Missense 11:55891231-55891231 + TCGA-A6-6141-01 COSM3752464 c.480C>T p.P160P Substitution - coding silent 11:55891230-55891230 + TCGA-AP-A0LI-01 COSM928144 c.261+1G>T p.? Unknown 11:55888263-55888263 + TCGA-AG-A002-01 COSM263855 c.758T>C p.F253S Substitution - Missense 11:55891508-55891508 + TCGA-CG-5726-01 COSM4033720 c.284+1G>C p.? Unknown 11:55889002-55889002 + TCGA-BR-8680-01 COSM4033725 c.475G>T p.D159Y Substitution - Missense 11:55891225-55891225 + TCGA-18-4721-01 COSM688780 c.369C>A p.L123L Substitution - coding silent 11:55890026-55890026 + TCGA-66-2780-01 COSM688774 c.657T>C p.F219F Substitution - coding silent 11:55891407-55891407 + SS6003113 COSM3716803 c.849T>C p.P283P Substitution - coding silent 11:55891599-55891599 + TCGA-E2-A10C-01 COSM429182 c.333C>T p.L111L Substitution - coding silent 11:55889990-55889990 + UM-SCC-17B COSM4599128 c.162T>A p.N54K Substitution - Missense 11:55888163-55888163 + TCGA-EE-A2ML-06 COSM3449079 c.52G>A p.E18K Substitution - Missense 11:55888053-55888053 + YUPEET COSM1703944 c.374G>A p.G125E Substitution - Missense 11:55890031-55890031 + SS6003115 COSM4033729 c.841T>C p.S281P Substitution - Missense 11:55891591-55891591 + 1517_CLM COSM5753714 c.146delT p.Q51fs*17 Deletion - Frameshift 11:55888147-55888147 + TCGA-GN-A263-01 COSM3449093 c.826C>T p.P276S Substitution - Missense 11:55891576-55891576 + TCGA-DU-5872-01 COSM3967593 c.127C>T p.R43* Substitution - Nonsense 11:55888128-55888128 + LUAD-U6SJ7 COSM358539 c.24C>A p.C8* Substitution - Nonsense 11:55886212-55886212 + TCGA-EL-A3T3-01 COSM3368411 c.831T>C p.N277N Substitution - coding silent 11:55891581-55891581 + SNUH_G16_S1 COSM3449091 c.491G>A p.G164E Substitution - Missense 11:55891241-55891241 + EGC3 COSM4195072 c.284+2T>G p.? Unknown 11:55889003-55889003 + TCGA-DB-5277-01 COSM3967595 c.818A>T p.Y273F Substitution - Missense 11:55891568-55891568 + TCGA-DA-A1HY-06 COSM3449081 c.97G>A p.E33K Substitution - Missense 11:55888098-55888098 + S02352 COSM5695274 c.350C>G p.T117S Substitution - Missense 11:55890007-55890007 + ICGC_MB34 COSM215472 c.284G>T p.R95M Substitution - Missense 11:55889001-55889001 + TCGA-BR-8589-01 COSM4033727 c.546T>C p.Y182Y Substitution - coding silent 11:55891296-55891296 + 2521243 COSM3449085 c.128G>A p.R43Q Substitution - Missense 11:55888129-55888129 + HN_62739 COSM129410 c.475G>A p.D159N Substitution - Missense 11:55891225-55891225 + CSCC-4-T COSM1703944 c.374G>A p.G125E Substitution - Missense 11:55890031-55890031 + 585208 COSM326561 c.114C>A p.H38Q Substitution - Missense 11:55888115-55888115 + LUAD-NYU408 COSM374038 c.663T>A p.L221L Substitution - coding silent 11:55891413-55891413 + SNUH_G26_S1 COSM3676187 c.820A>C p.T274P Substitution - Missense 11:55891570-55891570 + GC8_T COSM147214 c.491G>C p.G164A Substitution - Missense 11:55891241-55891241 + TCGA-AZ-4315-01 COSM1354508 c.205G>T p.G69* Substitution - Nonsense 11:55888206-55888206 + LUAD-CHTN-MAD08-00104 COSM361121 c.236A>G p.H79R Substitution - Missense 11:55888237-55888237 + QC2-39-T2 COSM5655665 c.793G>A p.D265N Substitution - Missense 11:55891543-55891543 + TCGA-ER-A19J-06 COSM363647 c.608G>A p.W203* Substitution - Nonsense 11:55891358-55891358 + CPCG0210-F1 COSM4966555 c.138C>A p.G46G Substitution - coding silent 11:55888139-55888139 + LUAD-NYU1021 COSM368014 c.780C>G p.T260T Substitution - coding silent 11:55891530-55891530 + TCGA-46-6025-01 COSM688772 c.720G>A p.V240V Substitution - coding silent 11:55891470-55891470 + TCGA-D3-A1Q6-06 COSM3449083 c.100G>A p.E34K Substitution - Missense 11:55888101-55888101 + TCGA-FW-A3R5-06 COSM192076 c.133G>A p.E45K Substitution - Missense 11:55888134-55888134 + TCGA-EE-A2A0-06 COSM3449091 c.491G>A p.G164E Substitution - Missense 11:55891241-55891241 + LUAD-74TBW COSM354987 c.173C>A p.A58D Substitution - Missense 11:55888174-55888174 + CPCG0047-F1 COSM4880156 c.274A>G p.I92V Substitution - Missense 11:55888991-55888991 + TCGA-FW-A3R5-06 COSM3449085 c.128G>A p.R43Q Substitution - Missense 11:55888129-55888129 + TCGA-06-0168-01 COSM3397805 c.421A>T p.I141F Substitution - Missense 11:55891171-55891171 + TCGA-BS-A0UV-01 COSM928146 c.661C>A p.L221I Substitution - Missense 11:55891411-55891411 + TCGA-76-4928-01 COSM3397802 c.78G>T p.K26N Substitution - Missense 11:55888079-55888079 + 1517_PT COSM5753714 c.146delT p.Q51fs*17 Deletion - Frameshift 11:55888147-55888147 + S00842 COSM5662134 c.857C>A p.P286H Substitution - Missense 11:55891607-55891607 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.326734 11q11

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.K57T c.170A>C 11 55653074 ESCA A C Missense p.K57T c.170A>C 11 55653074 HNSC A C Synonymous p.R223R c.667A>C 11 55655667 LUAD A - Frameshift p.M144Cfs*15 c.430delA 11 55653610 BLCA A - Frameshift p.M144Cfs*15 c.430delA 11 55653610 HNSC A - Frameshift p.M144Cfs*15 c.430delA 11 55653610 STAD - A Frameshift p.M144Nfs*10 c.430dupA 11 55653610 GBM - A Frameshift p.M144Nfs*10 c.430dupA 11 55653610 STAD A G Missense p.N213D c.637A>G 11 55655637 LUSC A G Missense p.R444G c.1330A>G 11 55659079 STAD A G Synonymous p.P25P c.75A>G 11 55652979 ESCA A G Synonymous p.R366R c.1098A>G 11 55658847 STAD A T Missense p.E134V c.401A>T 11 55653305 OV A T Missense p.E231V c.692A>T 11 55655692 ESCA A T Missense p.E264V c.791A>T 11 55657447 STAD A T Missense p.E54D c.162A>T 11 55653066 RCCC A T Missense p.H96L c.287A>T 11 55653191 NSCLC A T Missense p.I300F c.898A>T 11 55658647 GBM A T Missense p.Y432F c.1295A>T 11 55659044 LGG A T Synonymous p.I92I c.276A>T 11 55653180 HNSC C A 3-UTRSNV . c.1356+155C>A 11 55659260 ESCA C A Missense p.A47E c.140C>A 11 55653044 ESCA C A Missense p.D349E c.1047C>A 11 55658796 LUSC C A Missense p.D67E c.201C>A 11 55653105 RCCC C A Missense p.H197Q c.591C>A 11 55655591 GBM C A Missense p.H197Q c.591C>A 11 55655591 SCLC C A Missense p.L377I c.1129C>A 11 55658878 HNSC C A Missense p.N42K c.126C>A 11 55653030 LUAD C A Missense p.P435T c.1303C>A 11 55659052 LUAD C A Missense p.T66N c.197C>A 11 55653101 LUAD C A Synonymous p.L282L c.846C>A 11 55657502 LUSC C G Missense p.A335G c.1004C>G 11 55658753 LUAD C G Missense p.H121Q c.363C>G 11 55653267 HNSC C G Nonsense p.Y40* c.120C>G 11 55653024 LUAD C T IntronicSNV . c.412-70C>T 11 55653529 CM C T Missense p.H124Y c.370C>T 11 55653274 CM C T Missense p.H346Y c.1036C>T 11 55658785 BLCA C T Missense p.L64F c.190C>T 11 55653094 LUAD C T Missense p.P319L c.956C>T 11 55658705 LUAD C T Missense p.P435S c.1303C>T 11 55659052 CM C T Missense p.R83W c.247C>T 11 55653151 HNSC C T Missense p.T46M c.137C>T 11 55653041 GBM C T Missense p.T46M c.137C>T 11 55653041 UCEC C T Nonsense p.Q184* c.550C>T 11 55655550 CM C T Nonsense p.Q44* c.130C>T 11 55653034 LGG C T Nonsense p.R202* c.604C>T 11 55655604 LGG C T Synonymous p.C237C c.711C>T 11 55655711 CM C T Synonymous p.F412F c.1236C>T 11 55658985 CM C T Synonymous p.F9F c.27C>T 11 55652931 CM C T Synonymous p.I17I c.51C>T 11 55652955 LUAD C T Synonymous p.L41L c.123C>T 11 55653027 CM C T Synonymous p.T14T c.42C>T 11 55652946 CM G A Missense p.C69Y c.206G>A 11 55653110 RCCC G A Missense p.D318N c.952G>A 11 55658701 HNSC G A Missense p.E135K c.403G>A 11 55653307 CM G A Missense p.E149K c.445G>A 11 55653632 CM G A Missense p.E177K c.529G>A 11 55655529 CM G A Missense p.E192K c.574G>A 11 55655574 CM G A Missense p.E193K c.577G>A 11 55655577 CM G A Missense p.E204K c.610G>A 11 55655610 COREAD G A Missense p.E374K c.1120G>A 11 55658869 BRCA G A Missense p.E385K c.1153G>A 11 55658902 CM G A Missense p.G228R c.682G>A 11 55655682 CM G A Missense p.G323E c.968G>A 11 55658717 CM G A Missense p.M19I c.57G>A 11 55652961 CM G A Missense p.M73I c.219G>A 11 55653123 HNSC G A Missense p.R137Q c.410G>A 11 55653314 CM G A Missense p.S215N c.644G>A 11 55655644 CM G A Missense p.S281N c.842G>A 11 55657498 LUSC G A Nonsense p.W168* c.504G>A 11 55653691 BRCA G A Nonsense p.W362* c.1085G>A 11 55658834 CM G A Synonymous p.E385E c.1155G>A 11 55658904 CM G A Synonymous p.G94G c.282G>A 11 55653186 CM G A Synonymous p.P114P c.342G>A 11 55653246 GBM G A Synonymous p.R175R c.525G>A 11 55655525 CM G A Synonymous p.R36R c.108G>A 11 55653012 CM G A Synonymous p.T46T c.138G>A 11 55653042 LUAD G A Synonymous p.V399V c.1197G>A 11 55658946 LUSC GA TC Missense p.E98S c.292_293delinsTC 11 55653196 GBM G C Missense p.D314H c.940G>C 11 55658689 BLCA G C Missense p.D372H c.1114G>C 11 55658863 HNSC G C Missense p.E98D c.294G>C 11 55653198 HNSC G C Missense p.K101N c.303G>C 11 55653207 SCLC G C SpliceDonorSNV . c.761+1G>C 11 55656478 STAD GTG - InFrameDeletion p.V399delV c.1195_1197delGTG 11 55658941 HNSC G T Missense p.C167F c.500G>T 11 55653687 LUSC G T Missense p.C327F c.980G>T 11 55658729 BRCA G T Missense p.C93F c.278G>T 11 55653182 LUAD G T Missense p.D29Y c.85G>T 11 55652989 SCLC G T Missense p.D314Y c.940G>T 11 55658689 RCCC G T Missense p.E269D c.807G>T 11 55657463 LUSC G T Missense p.E98D c.294G>T 11 55653198 BRCA G T Missense p.G31V c.92G>T 11 55652996 UCEC G T Missense p.G376V c.1127G>T 11 55658876 CM G T Missense p.K185N c.555G>T 11 55655555 GBM G T Missense p.L6F c.18G>T 11 55652922 BRCA G T Missense p.M73I c.219G>T 11 55653123 NSCLC G T Missense p.R180I c.539G>T 11 55655539 LUSC G T Missense p.R254M c.761G>T 11 55656477 LUSC G T Missense p.R254M c.761G>T 11 55656477 MB G T Missense p.W131C c.393G>T 11 55653297 LUAD G T Missense p.W168L c.503G>T 11 55653690 LUAD G T Missense p.W343L c.1028G>T 11 55658777 LUAD G T SpliceDonorSNV . c.738+1G>T 11 55655739 UCEC G T Synonymous p.G273G c.819G>T 11 55657475 LUAD G T Synonymous p.L233L c.699G>T 11 55655699 LUAD G T Synonymous p.V398V c.1194G>T 11 55658943 HNSC T A IntronicSNV . c.738+37T>A 11 55655775 NSCLC T A Missense p.C389S c.1165T>A 11 55658914 GBM T A Missense p.F75Y c.224T>A 11 55653128 RCCC T A Missense p.L225H c.674T>A 11 55655674 ESCA T A Missense p.S395T c.1183T>A 11 55658932 LUAD T A Missense p.V242E c.725T>A 11 55655725 LUSC T A Missense p.W148R c.442T>A 11 55653629 MB T A Synonymous p.A181A c.543T>A 11 55655543 LUSC T C Missense p.W362R c.1084T>C 11 55658833 COREAD T C Synonymous p.F378F c.1134T>C 11 55658883 LUSC T C Synonymous p.N436N c.1308T>C 11 55659057 THCA T G IntronicSNV . c.412-23T>G 11 55653576 ESCA T G Missense p.C55G c.163T>G 11 55653067 HNSC T G Missense p.L379R c.1136T>G 11 55658885 STAD