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 21 37759967 37759967 + Silent SNP C C G TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr21:37759967C>G c.198C>G c.(196-198)acC>acG p.T66T BLCA 21 37766929 37766929 + Silent SNP C C T TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr21:37766929C>T c.462C>T c.(460-462)atC>atT p.I154I BLCA 21 37775096 37775096 + Missense_Mutation SNP C C G TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr21:37775096C>G c.704C>G c.(703-705)tCt>tGt p.S235C BLCA 21 37775105 37775105 + Missense_Mutation SNP G G A TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr21:37775105G>A c.713G>A c.(712-714)cGt>cAt p.R238H BLCA 21 37781087 37781087 + Silent SNP A A C TCGA-FD-A3B7-01A-31D-A20D-08 TCGA-FD-A3B7-10A-01D-A20D-08 g.chr21:37781087A>C c.786A>C c.(784-786)gtA>gtC p.V262V BLCA 21 37785282 37785282 + Missense_Mutation SNP C C A TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr21:37785282C>A c.1162C>A c.(1162-1164)Cca>Aca p.P388T BLCA 21 37785421 37785421 + Missense_Mutation SNP C C G TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chr21:37785421C>G c.1301C>G c.(1300-1302)cCc>cGc p.P434R BLCA 21 37788621 37788621 + Missense_Mutation SNP G G C TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr21:37788621G>C c.1637G>C c.(1636-1638)aGa>aCa p.R546T BRCA 21 37763873 37763873 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr21:37763873T>G c.284T>G c.(283-285)gTg>gGg p.V95G BRCA 21 37771831 37771831 + Silent SNP A A G TCGA-E9-A1N4-01A-11D-A14K-09 TCGA-E9-A1N4-10A-01D-A14K-09 g.chr21:37771831A>G c.591A>G c.(589-591)gtA>gtG p.V197V BRCA 21 37785375 37785375 + Missense_Mutation SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr21:37785375A>C c.1255A>C c.(1255-1257)Acc>Ccc p.T419P COAD 21 37759960 37759960 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr21:37759960G>A c.191G>A c.(190-192)cGt>cAt p.R64H COAD 21 37781679 37781679 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr21:37781679G>A c.835G>A c.(835-837)Gct>Act p.A279T COAD 21 37785221 37785221 + Silent SNP C C T TCGA-AZ-4682-01B-01D-1408-10 TCGA-AZ-4682-10A-01D-1408-10 g.chr21:37785221C>T c.1101C>T c.(1099-1101)gaC>gaT p.D367D COAD 21 37785464 37785464 + Silent SNP C C T TCGA-D5-6529-01A-11D-1771-10 TCGA-D5-6529-10A-01D-1771-10 g.chr21:37785464C>T c.1344C>T c.(1342-1344)gaC>gaT p.D448D COAD 21 37788591 37788591 + Missense_Mutation SNP A A G TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr21:37788591A>G c.1607A>G c.(1606-1608)cAg>cGg p.Q536R COAD 21 37788614 37788614 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr21:37788614C>T c.1630C>T c.(1630-1632)Cgg>Tgg p.R544W COADREAD 21 37759960 37759960 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr21:37759960G>A c.191G>A c.(190-192)cGt>cAt p.R64H COADREAD 21 37766863 37766863 + Silent SNP G G A TCGA-AG-A036-01A-12W-A096-10 TCGA-AG-A036-11A-11W-A096-10 g.chr21:37766863G>A c.396G>A c.(394-396)gtG>gtA p.V132V COADREAD 21 37781679 37781679 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr21:37781679G>A c.835G>A c.(835-837)Gct>Act p.A279T COADREAD 21 37785221 37785221 + Silent SNP C C T TCGA-AZ-4682-01B-01D-1408-10 TCGA-AZ-4682-10A-01D-1408-10 g.chr21:37785221C>T c.1101C>T c.(1099-1101)gaC>gaT p.D367D COADREAD 21 37785464 37785464 + Silent SNP C C T TCGA-D5-6529-01A-11D-1771-10 TCGA-D5-6529-10A-01D-1771-10 g.chr21:37785464C>T c.1344C>T c.(1342-1344)gaC>gaT p.D448D COADREAD 21 37788591 37788591 + Missense_Mutation SNP A A G TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr21:37788591A>G c.1607A>G c.(1606-1608)cAg>cGg p.Q536R COADREAD 21 37788614 37788614 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr21:37788614C>T c.1630C>T c.(1630-1632)Cgg>Tgg p.R544W DLBC 21 37787615 37787615 + Missense_Mutation SNP A A C TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr21:37787615A>C c.1516A>C c.(1516-1518)Aag>Cag p.K506Q ESCA 21 37771856 37771856 + Missense_Mutation SNP G G T TCGA-R6-A6XQ-01B-11D-A33E-09 TCGA-R6-A6XQ-10A-01D-A33H-09 g.chr21:37771856G>T c.616G>T c.(616-618)Gct>Tct p.A206S ESCA 21 37775142 37775142 + Silent SNP C C T TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr21:37775142C>T c.750C>T c.(748-750)ctC>ctT p.L250L ESCA 21 37781696 37781696 + Silent SNP T T C TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr21:37781696T>C c.852T>C c.(850-852)ccT>ccC p.P284P GBMLGG 21 37775114 37775114 + Missense_Mutation SNP G G C TCGA-DH-A66B-01A-11D-A29Q-08 TCGA-DH-A66B-10A-01D-A29Q-08 g.chr21:37775114G>C c.722G>C c.(721-723)aGt>aCt p.S241T GBMLGG 21 37785365 37785365 + Silent SNP G G A TCGA-QH-A6CX-01A-11D-A32B-08 TCGA-QH-A6CX-10A-01D-A329-08 g.chr21:37785365G>A c.1245G>A c.(1243-1245)ccG>ccA p.P415P GBMLGG 21 37787682 37787682 + Missense_Mutation SNP A A G TCGA-DU-6408-01A-11D-1705-08 TCGA-DU-6408-10A-01D-1705-08 g.chr21:37787682A>G c.1583A>G c.(1582-1584)cAg>cGg p.Q528R HNSC 21 37769777 37769777 + Silent SNP G G A TCGA-CV-7411-01A-11D-2078-08 TCGA-CV-7411-10A-01D-2078-08 g.chr21:37769777G>A c.546G>A c.(544-546)ttG>ttA p.L182L HNSC 21 37781744 37781744 + Silent SNP G G T TCGA-IQ-A61G-01A-11D-A30E-08 TCGA-IQ-A61G-10A-01D-A30H-08 g.chr21:37781744G>T c.900G>T c.(898-900)ctG>ctT p.L300L HNSC 21 37783871 37783871 + Missense_Mutation SNP A A T TCGA-CN-5364-01A-01D-1434-08 TCGA-CN-5364-10A-01D-1434-08 g.chr21:37783871A>T c.1030A>T c.(1030-1032)Ata>Tta p.I344L HNSC 21 37785298 37785298 + Missense_Mutation SNP G G T TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr21:37785298G>T c.1178G>T c.(1177-1179)aGa>aTa p.R393I HNSC 21 37785504 37785504 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr21:37785504G>A c.1384G>A c.(1384-1386)Ggg>Agg p.G462R HNSC 21 37788586 37788586 + Silent SNP C C T TCGA-CR-7383-01A-11D-2129-08 TCGA-CR-7383-10A-01D-2129-08 g.chr21:37788586C>T c.1602C>T c.(1600-1602)gaC>gaT p.D534D HNSC 21 37788639 37788639 + Missense_Mutation SNP G G A TCGA-CR-7395-01A-11D-2012-08 TCGA-CR-7395-10A-01D-2013-08 g.chr21:37788639G>A c.1655G>A c.(1654-1656)gGa>gAa p.G552E KIPAN 21 37783835 37783835 + Missense_Mutation SNP A A G TCGA-BP-5004-01A-01D-1462-08 TCGA-BP-5004-11A-01D-1462-08 g.chr21:37783835A>G c.994A>G c.(994-996)Acc>Gcc p.T332A KIPAN 21 37785583 37785583 + Missense_Mutation SNP C C G TCGA-CZ-4859-01A-02D-1429-08 TCGA-CZ-4859-11A-01D-1429-08 g.chr21:37785583C>G c.1463C>G c.(1462-1464)aCa>aGa p.T488R KIRC 21 37783835 37783835 + Missense_Mutation SNP A A G TCGA-BP-5004-01A-01D-1462-08 TCGA-BP-5004-11A-01D-1462-08 g.chr21:37783835A>G c.994A>G c.(994-996)Acc>Gcc p.T332A KIRC 21 37785583 37785583 + Missense_Mutation SNP C C G TCGA-CZ-4859-01A-02D-1429-08 TCGA-CZ-4859-11A-01D-1429-08 g.chr21:37785583C>G c.1463C>G c.(1462-1464)aCa>aGa p.T488R LGG 21 37775114 37775114 + Missense_Mutation SNP G G C TCGA-DH-A66B-01A-11D-A29Q-08 TCGA-DH-A66B-10A-01D-A29Q-08 g.chr21:37775114G>C c.722G>C c.(721-723)aGt>aCt p.S241T LGG 21 37785365 37785365 + Silent SNP G G A TCGA-QH-A6CX-01A-11D-A32B-08 TCGA-QH-A6CX-10A-01D-A329-08 g.chr21:37785365G>A c.1245G>A c.(1243-1245)ccG>ccA p.P415P LGG 21 37787682 37787682 + Missense_Mutation SNP A A G TCGA-DU-6408-01A-11D-1705-08 TCGA-DU-6408-10A-01D-1705-08 g.chr21:37787682A>G c.1583A>G c.(1582-1584)cAg>cGg p.Q528R LIHC 21 37785409 37785409 + Missense_Mutation SNP C C A TCGA-CC-A123-01A-11D-A12Z-10 TCGA-CC-A123-10A-01D-A12Z-10 g.chr21:37785409C>A c.1289C>A c.(1288-1290)cCc>cAc p.P430H LUAD 21 37758467 37758467 + Silent SNP C C T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr21:37758467C>T c.33C>T c.(31-33)caC>caT p.H11H LUAD 21 37758546 37758546 + Missense_Mutation SNP G G A TCGA-J2-8194-01A-11D-2238-08 TCGA-J2-8194-10A-01D-2238-08 g.chr21:37758546G>A c.112G>A c.(112-114)Gac>Aac p.D38N LUAD 21 37775077 37775077 + Missense_Mutation SNP C C T TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr21:37775077C>T c.685C>T c.(685-687)Cac>Tac p.H229Y LUAD 21 37775118 37775118 + Silent SNP C C T TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr21:37775118C>T c.726C>T c.(724-726)ttC>ttT p.F242F LUAD 21 37785246 37785246 + Missense_Mutation SNP G G C TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr21:37785246G>C c.1126G>C c.(1126-1128)Gag>Cag p.E376Q LUAD 21 37785450 37785450 + Missense_Mutation SNP A A G TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr21:37785450A>G c.1330A>G c.(1330-1332)Aca>Gca p.T444A LUSC 21 37763859 37763859 + Silent SNP C C A TCGA-37-4141-01A-02D-1352-08 TCGA-37-4141-10A-01D-1352-08 g.chr21:37763859C>A c.270C>A c.(268-270)atC>atA p.I90I LUSC 21 37775112 37775112 + Silent SNP G G T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr21:37775112G>T c.720G>T c.(718-720)ctG>ctT p.L240L LUSC 21 37788602 37788602 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr21:37788602C>T c.1618C>T c.(1618-1620)Cca>Tca p.P540S OV 21 37758546 37758546 + Missense_Mutation SNP G G T TCGA-13-0760-01A-01W-0372-09 TCGA-13-0760-10A-01W-0372-09 g.chr21:37758546G>T c.112G>T c.(112-114)Gac>Tac p.D38Y PAAD 21 37763902 37763902 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr21:37763902G>A c.313G>A c.(313-315)Gct>Act p.A105T PAAD 21 37769717 37769717 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr21:37769717A>G c.486A>G c.(484-486)caA>caG p.Q162Q PAAD 21 37781761 37781761 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr21:37781761C>T c.917C>T c.(916-918)aCa>aTa p.T306I PAAD 21 37783861 37783861 + Silent SNP C C T TCGA-2J-AAB1-01A-11D-A40W-08 TCGA-2J-AAB1-10A-01D-A40W-08 g.chr21:37783861C>T c.1020C>T c.(1018-1020)taC>taT p.Y340Y PRAD 21 37781094 37781094 + Missense_Mutation SNP A A G TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr21:37781094A>G c.793A>G c.(793-795)Acc>Gcc p.T265A READ 21 37766863 37766863 + Silent SNP G G A TCGA-AG-A036-01A-12W-A096-10 TCGA-AG-A036-11A-11W-A096-10 g.chr21:37766863G>A c.396G>A c.(394-396)gtG>gtA p.V132V SKCM 21 37766889 37766889 + Missense_Mutation SNP G G A TCGA-GN-A4U8-06A-11D-A32N-08 TCGA-GN-A4U8-10B-01D-A32N-08 g.chr21:37766889G>A c.422G>A c.(421-423)gGg>gAg p.G141E SKCM 21 37785199 37785199 + Missense_Mutation SNP T T G TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr21:37785199T>G c.1079T>G c.(1078-1080)tTc>tGc p.F360C SKCM 21 37785272 37785272 + Silent SNP G G A TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr21:37785272G>A c.1152G>A c.(1150-1152)ttG>ttA p.L384L SKCM 21 37785495 37785495 + Missense_Mutation SNP C C T TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr21:37785495C>T c.1375C>T c.(1375-1377)Ccc>Tcc p.P459S SKCM 21 37785496 37785496 + Missense_Mutation SNP C C T TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr21:37785496C>T c.1376C>T c.(1375-1377)cCc>cTc p.P459L SKCM 21 37788600 37788600 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr21:37788600C>T c.1616C>T c.(1615-1617)cCc>cTc p.P539L BLCA 10 28345491 28345491 + Missense_Mutation SNP G G A TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr10:28345491G>A c.1469C>T c.(1468-1470)tCa>tTa p.S490L BLCA 10 28348590 28348590 + Silent SNP T T C TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr10:28348590T>C c.1287A>G c.(1285-1287)gtA>gtG p.V429V BLCA 10 28358781 28358781 + Splice_Site SNP C C A TCGA-E7-A3Y1-01A-11D-A22Z-08 TCGA-E7-A3Y1-10A-01D-A22Z-08 g.chr10:28358781C>A c.1124G>T c.(1123-1125)gGt>gTt p.G375V BLCA 10 28358782 28358782 + Splice_Site SNP C C A TCGA-E7-A3Y1-01A-11D-A22Z-08 TCGA-E7-A3Y1-10A-01D-A22Z-08 g.chr10:28358782C>A c.e13-1 BLCA 10 28378735 28378735 + Missense_Mutation SNP C C G TCGA-4Z-AA7R-01A-11D-A391-08 TCGA-4Z-AA7R-10A-01D-A394-08 g.chr10:28378735C>G c.988G>C c.(988-990)Gat>Cat p.D330H BLCA 10 28409311 28409311 + Missense_Mutation SNP G G C TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr10:28409311G>C c.699C>G c.(697-699)atC>atG p.I233M BLCA 10 28420612 28420612 + Silent SNP G G A TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr10:28420612G>A c.324C>T c.(322-324)ctC>ctT p.L108L BLCA 10 28491177 28491177 + Missense_Mutation SNP G G C TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr10:28491177G>C c.61C>G c.(61-63)Ctg>Gtg p.L21V BLCA 10 28527520 28527520 + Missense_Mutation SNP G G A TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr10:28527520G>A c.14C>T c.(13-15)tCa>tTa p.S5L BRCA 10 28378743 28378743 + Missense_Mutation SNP C C G TCGA-EW-A1P4-01A-21D-A142-09 TCGA-EW-A1P4-10A-01D-A142-09 g.chr10:28378743C>G c.980G>C c.(979-981)aGt>aCt p.S327T BRCA 10 28409186 28409186 + Missense_Mutation SNP G G C TCGA-B6-A400-01A-11D-A23C-09 TCGA-B6-A400-10A-01D-A23C-09 g.chr10:28409186G>C c.824C>G c.(823-825)gCg>gGg p.A275G BRCA 10 28412995 28412995 + Nonsense_Mutation SNP C C A TCGA-AC-A62Y-01A-11D-A29N-09 TCGA-AC-A62Y-10A-01D-A29N-09 g.chr10:28412995C>A c.580G>T c.(580-582)Gag>Tag p.E194* BRCA 10 28436429 28436429 + Missense_Mutation SNP A A G TCGA-B6-A0I5-01A-11W-A100-09 TCGA-B6-A0I5-10A-01W-A055-09 g.chr10:28436429A>G c.298T>C c.(298-300)Tca>Cca p.S100P CESC 10 28358735 28358735 + Silent SNP G G A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr10:28358735G>A c.1170C>T c.(1168-1170)atC>atT p.I390I CESC 10 28408627 28408627 + Missense_Mutation SNP C C T TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr10:28408627C>T c.905G>A c.(904-906)cGa>cAa p.R302Q CESC 10 28420622 28420622 + Splice_Site SNP T T C TCGA-C5-A7CJ-01A-11D-A32I-09 TCGA-C5-A7CJ-10A-01D-A32I-09 g.chr10:28420622T>C c.e6-2 CHOL 10 28413008 28413008 + Silent SNP G G A TCGA-W5-AA38-01A-11D-A417-09 TCGA-W5-AA38-10A-01D-A41A-09 g.chr10:28413008G>A c.567C>T c.(565-567)aaC>aaT p.N189N COAD 10 28343103 28343103 + Missense_Mutation SNP T T C TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr10:28343103T>C c.1622A>G c.(1621-1623)aAa>aGa p.K541R COAD 10 28347489 28347489 + Missense_Mutation SNP T T A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr10:28347489T>A c.1342A>T c.(1342-1344)Agt>Tgt p.S448C COAD 10 28408644 28408644 + Splice_Site SNP C C T TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr10:28408644C>T c.888G>A c.(886-888)agG>agA p.R296R COAD 10 28408646 28408646 + Splice_Site SNP T T C TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr10:28408646T>C c.e11-2 COAD 10 28408646 28408646 + Splice_Site SNP T T C TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr10:28408646T>C c.e11-2 COADREAD 10 28343023 28343023 + Missense_Mutation SNP A A T TCGA-AF-2691-01A-01W-0831-10 TCGA-AF-2691-10A-01W-0831-10 g.chr10:28343023A>T c.1702T>A c.(1702-1704)Tgg>Agg p.W568R COADREAD 10 28343103 28343103 + Missense_Mutation SNP T T C TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr10:28343103T>C c.1622A>G c.(1621-1623)aAa>aGa p.K541R COADREAD 10 28347489 28347489 + Missense_Mutation SNP T T A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr10:28347489T>A c.1342A>T c.(1342-1344)Agt>Tgt p.S448C COADREAD 10 28348654 28348654 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:28348654C>A c.1223G>T c.(1222-1224)aGa>aTa p.R408I COADREAD 10 28408644 28408644 + Splice_Site SNP C C T TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr10:28408644C>T c.888G>A c.(886-888)agG>agA p.R296R COADREAD 10 28408646 28408646 + Splice_Site SNP T T C TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr10:28408646T>C c.e11-2 COADREAD 10 28408646 28408646 + Splice_Site SNP T T C TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr10:28408646T>C c.e11-2 COADREAD 10 28420579 28420579 + Silent SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr10:28420579G>A c.357C>T c.(355-357)taC>taT p.Y119Y COADREAD 10 28527516 28527516 + Silent SNP C C T TCGA-AG-3608-01A-01W-0833-10 TCGA-AG-3608-10A-01W-0833-10 g.chr10:28527516C>T c.18G>A c.(16-18)acG>acA p.T6T DLBC 10 28412969 28412969 + Missense_Mutation SNP T T C TCGA-FF-8042-01A-11D-2210-10 TCGA-FF-8042-10A-01D-2210-10 g.chr10:28412969T>C c.606A>G c.(604-606)atA>atG p.I202M DLBC 10 28420542 28420542 + Missense_Mutation SNP C C T TCGA-FF-A7CW-01A-11D-A382-10 TCGA-FF-A7CW-10A-01D-A385-10 g.chr10:28420542C>T c.394G>A c.(394-396)Gat>Aat p.D132N DLBC 10 28527517 28527517 + Missense_Mutation SNP G G A TCGA-FF-8047-01A-11D-2210-10 TCGA-FF-8047-10A-01D-2210-10 g.chr10:28527517G>A c.17C>T c.(16-18)aCg>aTg p.T6M ESCA 10 28348649 28348649 + Missense_Mutation SNP G G T TCGA-IG-A6QS-01A-12D-A33E-09 TCGA-IG-A6QS-10B-01D-A33H-09 g.chr10:28348649G>T c.1228C>A c.(1228-1230)Cag>Aag p.Q410K ESCA 10 28378763 28378763 + Silent SNP A A G TCGA-2H-A9GH-01A-11D-A37C-09 TCGA-2H-A9GH-11A-11D-A37F-09 g.chr10:28378763A>G c.960T>C c.(958-960)ttT>ttC p.F320F GBM 10 28345469 28345469 + Silent SNP T T C TCGA-27-1833-01A-01W-0643-08 TCGA-27-1833-10A-01W-0644-08 g.chr10:28345469T>C c.1491A>G c.(1489-1491)acA>acG p.T497T GBM 10 28378639 28378639 + Nonsense_Mutation SNP G G A TCGA-27-2521-01A-01D-1494-08 TCGA-27-2521-10A-01D-1494-08 g.chr10:28378639G>A c.1084C>T c.(1084-1086)Cga>Tga p.R362* GBM 10 28409253 28409254 + Missense_Mutation DNP CA CA AG TCGA-02-2483-01A-01D-1494-08 TCGA-02-2483-10A-01D-1494-08 g.chr10:28409253_28409254CA>AG c.756_757TG>CT c.(754-759)gcTGgg>gcCTgg p.G253W GBM 10 28420514 28420514 + Missense_Mutation SNP C C T TCGA-06-0213-01A-01D-1491-08 TCGA-06-0213-10A-01D-1491-08 g.chr10:28420514C>T c.422G>A c.(421-423)cGt>cAt p.R141H GBMLGG 10 28345469 28345469 + Silent SNP T T C TCGA-27-1833-01A-01W-0643-08 TCGA-27-1833-10A-01W-0644-08 g.chr10:28345469T>C c.1491A>G c.(1489-1491)acA>acG p.T497T GBMLGG 10 28345529 28345529 + Silent SNP T T C TCGA-HW-8319-01A-11D-2395-08 TCGA-HW-8319-10A-01D-2396-08 g.chr10:28345529T>C c.1431A>G c.(1429-1431)ctA>ctG p.L477L GBMLGG 10 28348654 28348654 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:28348654C>A c.1223G>T c.(1222-1224)aGa>aTa p.R408I GBMLGG 10 28358723 28358723 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:28358723C>T c.1182G>A c.(1180-1182)caG>caA p.Q394Q GBMLGG 10 28378639 28378639 + Nonsense_Mutation SNP G G A TCGA-27-2521-01A-01D-1494-08 TCGA-27-2521-10A-01D-1494-08 g.chr10:28378639G>A c.1084C>T c.(1084-1086)Cga>Tga p.R362* GBMLGG 10 28378749 28378749 + Missense_Mutation SNP C C T TCGA-DU-A5TP-01A-11D-A289-08 TCGA-DU-A5TP-10A-01D-A289-08 g.chr10:28378749C>T c.974G>A c.(973-975)cGt>cAt p.R325H GBMLGG 10 28378749 28378749 + Missense_Mutation SNP C C T TCGA-S9-A6UA-01A-12D-A33T-08 TCGA-S9-A6UA-10A-01D-A33W-08 g.chr10:28378749C>T c.974G>A c.(973-975)cGt>cAt p.R325H GBMLGG 10 28409253 28409254 + Missense_Mutation DNP CA CA AG TCGA-02-2483-01A-01D-1494-08 TCGA-02-2483-10A-01D-1494-08 g.chr10:28409253_28409254CA>AG c.756_757TG>CT c.(754-759)gcTGgg>gcCTgg p.G253W GBMLGG 10 28414006 28414006 + Silent SNP C C T TCGA-HT-8563-01A-11D-2395-08 TCGA-HT-8563-10A-01D-2396-08 g.chr10:28414006C>T c.462G>A c.(460-462)aaG>aaA p.K154K GBMLGG 10 28420514 28420514 + Missense_Mutation SNP C C T TCGA-06-0213-01A-01D-1491-08 TCGA-06-0213-10A-01D-1491-08 g.chr10:28420514C>T c.422G>A c.(421-423)cGt>cAt p.R141H HNSC 10 28378644 28378644 + Missense_Mutation SNP T T C TCGA-BA-A6DG-01A-21D-A30E-08 TCGA-BA-A6DG-10A-01D-A30H-08 g.chr10:28378644T>C c.1079A>G c.(1078-1080)tAt>tGt p.Y360C HNSC 10 28409159 28409159 + Missense_Mutation SNP C C A TCGA-F7-A61S-01A-11D-A28R-08 TCGA-F7-A61S-10A-01D-A28U-08 g.chr10:28409159C>A c.851G>T c.(850-852)aGg>aTg p.R284M HNSC 10 28409531 28409531 + Missense_Mutation SNP C C G TCGA-CN-A49B-01A-31D-A24D-08 TCGA-CN-A49B-10A-01D-A24F-08 g.chr10:28409531C>G c.682G>C c.(682-684)Gaa>Caa p.E228Q HNSC 10 28413008 28413008 + Silent SNP G G A TCGA-CV-6436-01A-11D-1683-08 TCGA-CV-6436-11A-01D-1683-08 g.chr10:28413008G>A c.567C>T c.(565-567)aaC>aaT p.N189N HNSC 10 28413037 28413037 + Missense_Mutation SNP G G A TCGA-CN-A6V7-01A-12D-A34J-08 TCGA-CN-A6V7-10A-01D-A34M-08 g.chr10:28413037G>A c.538C>T c.(538-540)Cat>Tat p.H180Y LGG 10 28345529 28345529 + Silent SNP T T C TCGA-HW-8319-01A-11D-2395-08 TCGA-HW-8319-10A-01D-2396-08 g.chr10:28345529T>C c.1431A>G c.(1429-1431)ctA>ctG p.L477L LGG 10 28348654 28348654 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:28348654C>A c.1223G>T c.(1222-1224)aGa>aTa p.R408I LGG 10 28358723 28358723 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:28358723C>T c.1182G>A c.(1180-1182)caG>caA p.Q394Q LGG 10 28378749 28378749 + Missense_Mutation SNP C C T TCGA-DU-A5TP-01A-11D-A289-08 TCGA-DU-A5TP-10A-01D-A289-08 g.chr10:28378749C>T c.974G>A c.(973-975)cGt>cAt p.R325H LGG 10 28378749 28378749 + Missense_Mutation SNP C C T TCGA-S9-A6UA-01A-12D-A33T-08 TCGA-S9-A6UA-10A-01D-A33W-08 g.chr10:28378749C>T c.974G>A c.(973-975)cGt>cAt p.R325H LGG 10 28414006 28414006 + Silent SNP C C T TCGA-HT-8563-01A-11D-2395-08 TCGA-HT-8563-10A-01D-2396-08 g.chr10:28414006C>T c.462G>A c.(460-462)aaG>aaA p.K154K LIHC 10 28378706 28378706 + Silent SNP T T C TCGA-DD-A4NV-01A-11D-A30V-10 TCGA-DD-A4NV-10A-01D-A30V-10 g.chr10:28378706T>C c.1017A>G c.(1015-1017)gaA>gaG p.E339E LIHC 10 28420525 28420525 + Silent SNP T T C TCGA-BC-A10T-01A-11D-A12Z-10 TCGA-BC-A10T-11A-11D-A12Z-10 g.chr10:28420525T>C c.411A>G c.(409-411)gtA>gtG p.V137V LIHC 10 28491163 28491163 + Silent SNP C C A TCGA-DD-AACK-01A-11D-A40R-10 TCGA-DD-AACK-10A-01D-A40U-10 g.chr10:28491163C>A c.75G>T c.(73-75)ctG>ctT p.L25L LUAD 10 28348647 28348647 + Silent SNP C C T TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr10:28348647C>T c.1230G>A c.(1228-1230)caG>caA p.Q410Q LUAD 10 28378646 28378646 + Silent SNP C C A TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr10:28378646C>A c.1077G>T c.(1075-1077)ccG>ccT p.P359P LUSC 10 28345494 28345494 + Missense_Mutation SNP G G T TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr10:28345494G>T c.1466C>A c.(1465-1467)cCa>cAa p.P489Q LUSC 10 28345547 28345547 + Silent SNP C C T TCGA-34-5928-01A-11D-1817-08 TCGA-34-5928-10A-01D-1817-08 g.chr10:28345547C>T c.1413G>A c.(1411-1413)gtG>gtA p.V471V LUSC 10 28348580 28348580 + Splice_Site SNP T T C TCGA-22-5480-01A-01D-1632-08 TCGA-22-5480-11A-01D-1632-08 g.chr10:28348580T>C c.1297A>G c.(1297-1299)Aag>Gag p.K433E LUSC 10 28348635 28348635 + Silent SNP A A T TCGA-51-4080-01A-01D-1458-08 TCGA-51-4080-11A-01D-1458-08 g.chr10:28348635A>T c.1242T>A c.(1240-1242)ggT>ggA p.G414G LUSC 10 28348669 28348669 + Missense_Mutation SNP G G A TCGA-39-5035-01A-01D-1441-08 TCGA-39-5035-11A-01D-1441-08 g.chr10:28348669G>A c.1208C>T c.(1207-1209)aCc>aTc p.T403I LUSC 10 28420572 28420572 + Missense_Mutation SNP C C A TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr10:28420572C>A c.364G>T c.(364-366)Gtg>Ttg p.V122L OV 10 28378746 28378746 + Missense_Mutation SNP A A C TCGA-04-1644-01B-01D-1526-09 TCGA-04-1644-11A-01D-1526-09 g.chr10:28378746A>C c.977T>G c.(976-978)cTt>cGt p.L326R OV 10 28408644 28408644 + Splice_Site SNP C C G TCGA-13-1412-01A-01W-0494-09 TCGA-13-1412-10A-01W-0495-09 g.chr10:28408644C>G c.888G>C c.(886-888)agG>agC p.R296S PAAD 10 28345483 28345483 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:28345483G>A c.1477C>T c.(1477-1479)Cgt>Tgt p.R493C PAAD 10 28412986 28412986 + Frame_Shift_Del DEL T T - TCGA-IB-A7LX-01A-12D-A36O-08 TCGA-IB-A7LX-10A-01D-A367-08 g.chr10:28412986delT c.589delA c.(589-591)aggfs p.R197fs PRAD 10 28358764 28358764 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:28358764G>A c.1141C>T c.(1141-1143)Ctg>Ttg p.L381L READ 10 28343023 28343023 + Missense_Mutation SNP A A T TCGA-AF-2691-01A-01W-0831-10 TCGA-AF-2691-10A-01W-0831-10 g.chr10:28343023A>T c.1702T>A c.(1702-1704)Tgg>Agg p.W568R READ 10 28348654 28348654 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:28348654C>A c.1223G>T c.(1222-1224)aGa>aTa p.R408I READ 10 28420579 28420579 + Silent SNP G G A TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr10:28420579G>A c.357C>T c.(355-357)taC>taT p.Y119Y READ 10 28527516 28527516 + Silent SNP C C T TCGA-AG-3608-01A-01W-0833-10 TCGA-AG-3608-10A-01W-0833-10 g.chr10:28527516C>T c.18G>A c.(16-18)acG>acA p.T6T SKCM 10 28343065 28343065 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:28343065C>T c.1660G>A c.(1660-1662)Gag>Aag p.E554K SKCM 10 28343131 28343131 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr10:28343131C>T c.1594G>A c.(1594-1596)Gaa>Aaa p.E532K SKCM 10 28345429 28345429 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr10:28345429C>T c.1531G>A c.(1531-1533)Ggt>Agt p.G511S SKCM 10 28347511 28347511 + Nonsense_Mutation SNP A A T TCGA-EE-A29A-06A-12D-A196-08 TCGA-EE-A29A-10A-01D-A198-08 g.chr10:28347511A>T c.1320T>A c.(1318-1320)taT>taA p.Y440* SKCM 10 28347518 28347518 + Missense_Mutation SNP C C T TCGA-EE-A29C-06A-21D-A197-08 TCGA-EE-A29C-10A-01D-A199-08 g.chr10:28347518C>T c.1313G>A c.(1312-1314)gGa>gAa p.G438E SKCM 10 28347533 28347533 + Splice_Site SNP C C T TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chr10:28347533C>T c.e15-1 SKCM 10 28348640 28348640 + Missense_Mutation SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr10:28348640C>T c.1237G>A c.(1237-1239)Gat>Aat p.D413N SKCM 10 28348673 28348673 + Splice_Site SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:28348673C>T c.e14-1 SKCM 10 28358748 28358748 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr10:28358748C>T c.1157G>A c.(1156-1158)cGa>cAa p.R386Q SKCM 10 28358748 28358748 + Missense_Mutation SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr10:28358748C>T c.1157G>A c.(1156-1158)cGa>cAa p.R386Q SKCM 10 28358748 28358748 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr10:28358748C>T c.1157G>A c.(1156-1158)cGa>cAa p.R386Q SKCM 10 28358748 28358748 + Missense_Mutation SNP C C T TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr10:28358748C>T c.1157G>A c.(1156-1158)cGa>cAa p.R386Q SKCM 10 28378638 28378638 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:28378638C>T c.1085G>A c.(1084-1086)cGa>cAa p.R362Q SKCM 10 28378648 28378648 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr10:28378648G>A c.1075C>T c.(1075-1077)Ccg>Tcg p.P359S SKCM 10 28378660 28378660 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr10:28378660C>T c.1063G>A c.(1063-1065)Gaa>Aaa p.E355K SKCM 10 28378660 28378660 + Missense_Mutation SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr10:28378660C>T c.1063G>A c.(1063-1065)Gaa>Aaa p.E355K SKCM 10 28378684 28378684 + Missense_Mutation SNP C C T TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr10:28378684C>T c.1039G>A c.(1039-1041)Gac>Aac p.D347N SKCM 10 28378716 28378716 + Missense_Mutation SNP G G A TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr10:28378716G>A c.1007C>T c.(1006-1008)tCc>tTc p.S336F SKCM 10 28378745 28378745 + Silent SNP A A G TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr10:28378745A>G c.978T>C c.(976-978)ctT>ctC p.L326L SKCM 10 28378750 28378750 + Missense_Mutation SNP G G A TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr10:28378750G>A c.973C>T c.(973-975)Cgt>Tgt p.R325C SKCM 10 28408587 28408587 + Silent SNP C C T TCGA-D3-A2J7-06A-11D-A196-08 TCGA-D3-A2J7-10A-01D-A198-08 g.chr10:28408587C>T c.945G>A c.(943-945)agG>agA p.R315R SKCM 10 28409123 28409123 + Splice_Site SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:28409123C>T c.887G>A c.(886-888)aGg>aAg p.R296K SKCM 10 28409131 28409131 + Silent SNP G G A TCGA-ER-A199-06A-11D-A197-08 TCGA-ER-A199-10A-01D-A199-08 g.chr10:28409131G>A c.879C>T c.(877-879)ttC>ttT p.F293F SKCM 10 28409178 28409178 + Missense_Mutation SNP C C T TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr10:28409178C>T c.832G>A c.(832-834)Gaa>Aaa p.E278K SKCM 10 28409221 28409221 + Silent SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr10:28409221C>T c.789G>A c.(787-789)caG>caA p.Q263Q SKCM 10 28409223 28409223 + Nonsense_Mutation SNP G G A TCGA-ER-A19J-06A-11D-A196-08 TCGA-ER-A19J-10A-01D-A198-08 g.chr10:28409223G>A c.787C>T c.(787-789)Cag>Tag p.Q263* SKCM 10 28409238 28409238 + Missense_Mutation SNP T T G TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr10:28409238T>G c.772A>C c.(772-774)Aag>Cag p.K258Q SKCM 10 28409259 28409259 + Missense_Mutation SNP C C T TCGA-EE-A2GU-06A-11D-A196-08 TCGA-EE-A2GU-10A-01D-A198-08 g.chr10:28409259C>T c.751G>A c.(751-753)Gaa>Aaa p.E251K SKCM 10 28409259 28409259 + Missense_Mutation SNP C C T TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr10:28409259C>T c.751G>A c.(751-753)Gaa>Aaa p.E251K SKCM 10 28409261 28409261 + Missense_Mutation SNP T T C TCGA-GN-A4U3-06A-11D-A32N-08 TCGA-GN-A4U3-10F-01D-A32N-08 g.chr10:28409261T>C c.749A>G c.(748-750)aAg>aGg p.K250R SKCM 10 28409262 28409262 + Missense_Mutation SNP T T C TCGA-GN-A4U3-06A-11D-A32N-08 TCGA-GN-A4U3-10F-01D-A32N-08 g.chr10:28409262T>C c.748A>G c.(748-750)Aag>Gag p.K250E SKCM 10 28409304 28409304 + Missense_Mutation SNP G G A TCGA-D3-A5GS-06A-11D-A27K-08 TCGA-D3-A5GS-10A-01D-A27N-08 g.chr10:28409304G>A c.706C>T c.(706-708)Ctc>Ttc p.L236F SKCM 10 28409531 28409531 + Missense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr10:28409531C>T c.682G>A c.(682-684)Gaa>Aaa p.E228K SKCM 10 28412977 28412977 + Missense_Mutation SNP C C T TCGA-FS-A4F9-06A-11D-A24R-08 TCGA-FS-A4F9-10A-01D-A24R-08 g.chr10:28412977C>T c.598G>A c.(598-600)Gaa>Aaa p.E200K SKCM 10 28413985 28413985 + Silent SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr10:28413985C>T c.483G>A c.(481-483)gcG>gcA p.A161A SKCM 10 28414002 28414002 + Missense_Mutation SNP C C T TCGA-FS-A1ZB-06A-12D-A197-08 TCGA-FS-A1ZB-10A-01D-A199-08 g.chr10:28414002C>T c.466G>A c.(466-468)Gat>Aat p.D156N SKCM 10 28420502 28420502 + Missense_Mutation SNP T T A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:28420502T>A c.434A>T c.(433-435)aAt>aTt p.N145I SKCM 10 28420515 28420515 + Missense_Mutation SNP G G A TCGA-GN-A268-06A-11D-A196-08 TCGA-GN-A268-10A-01D-A198-08 g.chr10:28420515G>A c.421C>T c.(421-423)Cgt>Tgt p.R141C SKCM 10 28420537 28420537 + Silent SNP C C T TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr10:28420537C>T c.399G>A c.(397-399)gaG>gaA p.E133E SKCM 10 28420539 28420539 + Missense_Mutation SNP C C T TCGA-ER-A19N-06A-11D-A197-08 TCGA-ER-A19N-10A-01D-A199-08 g.chr10:28420539C>T c.397G>A c.(397-399)Gag>Aag p.E133K SKCM 10 28420551 28420551 + Missense_Mutation SNP C C T TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr10:28420551C>T c.385G>A c.(385-387)Gat>Aat p.D129N SKCM 10 28420556 28420556 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr10:28420556G>A c.380C>T c.(379-381)cCt>cTt p.P127L SKCM 10 28420578 28420578 + Missense_Mutation SNP C C T TCGA-D3-A1QA-06A-11D-A196-08 TCGA-D3-A1QA-10A-01D-A198-08 g.chr10:28420578C>T c.358G>A c.(358-360)Gac>Aac p.D120N SKCM 10 28420578 28420578 + Missense_Mutation SNP C C T TCGA-D3-A5GS-06A-11D-A27K-08 TCGA-D3-A5GS-10A-01D-A27N-08 g.chr10:28420578C>T c.358G>A c.(358-360)Gac>Aac p.D120N SKCM 10 28420578 28420578 + Missense_Mutation SNP C C T TCGA-D9-A149-06A-11D-A196-08 TCGA-D9-A149-10A-01D-A198-08 g.chr10:28420578C>T c.358G>A c.(358-360)Gac>Aac p.D120N SKCM 10 28491141 28491141 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr10:28491141C>T c.97G>A c.(97-99)Gaa>Aaa p.E33K

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 21 37785572 37785572 single base substitution C T downstream_gene_variant BLCA-CN 21 37785572 37785572 single base substitution C T synonymous_variant V484V 1452C>T BLCA-US 21 37781087 37781087 single base substitution A C intron_variant BLCA-US 21 37781087 37781087 single base substitution A C synonymous_variant V262V 786A>C BOCA-UK 21 37758473 37758473 single base substitution G T exon_variant BOCA-UK 21 37758473 37758473 single base substitution G T missense_variant K13N 39G>T BOCA-UK 21 37758507 37758507 single base substitution A G exon_variant BOCA-UK 21 37758507 37758507 single base substitution A G missense_variant T25A 73A>G BRCA-EU 21 37752771 37752771 deletion of <=200bp T - upstream_gene_variant BRCA-EU 21 37753431 37753433 deletion of <=200bp TTC - upstream_gene_variant BRCA-EU 21 37755237 37755237 single base substitution C T upstream_gene_variant BRCA-EU 21 37756575 37756575 single base substitution G A upstream_gene_variant BRCA-EU 21 37759266 37759266 single base substitution C T intron_variant BRCA-EU 21 37759326 37759326 single base substitution G T intron_variant BRCA-EU 21 37759448 37759448 single base substitution T G intron_variant BRCA-EU 21 37760061 37760061 single base substitution G A intron_variant BRCA-EU 21 37760134 37760134 single base substitution G A intron_variant BRCA-EU 21 37760838 37760838 single base substitution C G intron_variant BRCA-EU 21 37761057 37761057 single base substitution G A intron_variant BRCA-EU 21 37761843 37761843 single base substitution C T intron_variant BRCA-EU 21 37763902 37763902 single base substitution G A exon_variant BRCA-EU 21 37763902 37763902 single base substitution G A missense_variant A105T 313G>A BRCA-EU 21 37764995 37764995 single base substitution G A intron_variant BRCA-EU 21 37766760 37766760 single base substitution G A intron_variant BRCA-EU 21 37768424 37768424 single base substitution G T intron_variant BRCA-EU 21 37768424 37768424 single base substitution G T upstream_gene_variant BRCA-EU 21 37771557 37771557 single base substitution C G downstream_gene_variant BRCA-EU 21 37771557 37771557 single base substitution C G intron_variant BRCA-EU 21 37771557 37771557 single base substitution C G upstream_gene_variant BRCA-EU 21 37772199 37772199 single base substitution G A downstream_gene_variant BRCA-EU 21 37772199 37772199 single base substitution G A intron_variant BRCA-EU 21 37772840 37772840 single base substitution T C downstream_gene_variant BRCA-EU 21 37772840 37772840 single base substitution T C intron_variant BRCA-EU 21 37774678 37774678 single base substitution C G downstream_gene_variant BRCA-EU 21 37774678 37774678 single base substitution C G intron_variant BRCA-EU 21 37778947 37778947 insertion of <=200bp - TA intron_variant BRCA-EU 21 37781395 37781395 single base substitution C T intron_variant BRCA-EU 21 37783068 37783068 single base substitution C T intron_variant BRCA-EU 21 37784224 37784224 single base substitution G A intron_variant BRCA-EU 21 37785075 37785075 single base substitution G A exon_variant BRCA-EU 21 37785075 37785075 single base substitution G A intron_variant BRCA-EU 21 37787126 37787126 single base substitution G A downstream_gene_variant BRCA-EU 21 37787126 37787126 single base substitution G A intron_variant BRCA-EU 21 37788604 37788604 single base substitution A G downstream_gene_variant BRCA-EU 21 37788604 37788604 single base substitution A G synonymous_variant P540P 1620A>G BRCA-EU 21 37789677 37789677 single base substitution G A 3_prime_UTR_variant BRCA-EU 21 37789677 37789677 single base substitution G A downstream_gene_variant BRCA-EU 21 37790156 37790156 single base substitution C T 3_prime_UTR_variant BRCA-EU 21 37790156 37790156 single base substitution C T downstream_gene_variant BRCA-EU 21 37791726 37791726 single base substitution G T downstream_gene_variant BRCA-FR 21 37789673 37789673 single base substitution G A 3_prime_UTR_variant BRCA-FR 21 37789673 37789673 single base substitution G A downstream_gene_variant BRCA-UK 21 37759448 37759448 single base substitution T G intron_variant BRCA-UK 21 37780692 37780692 single base substitution C G intron_variant BRCA-UK 21 37781550 37781550 single base substitution C T intron_variant BRCA-UK 21 37785375 37785375 single base substitution A C downstream_gene_variant BRCA-UK 21 37785375 37785375 single base substitution A C missense_variant T419P 1255A>C BRCA-UK 21 37789983 37789983 single base substitution C T 3_prime_UTR_variant BRCA-UK 21 37789983 37789983 single base substitution C T downstream_gene_variant BRCA-UK 21 37790156 37790156 single base substitution C T 3_prime_UTR_variant BRCA-UK 21 37790156 37790156 single base substitution C T downstream_gene_variant BRCA-US 21 37763873 37763873 single base substitution T G exon_variant BRCA-US 21 37763873 37763873 single base substitution T G missense_variant V95G 284T>G BRCA-US 21 37771831 37771831 single base substitution A G downstream_gene_variant BRCA-US 21 37771831 37771831 single base substitution A G exon_variant BRCA-US 21 37771831 37771831 single base substitution A G synonymous_variant V197V 591A>G BRCA-US 21 37785375 37785375 single base substitution A C downstream_gene_variant BRCA-US 21 37785375 37785375 single base substitution A C missense_variant T419P 1255A>C BTCA-JP 21 37769702 37769702 single base substitution T G intron_variant BTCA-JP 21 37769702 37769702 single base substitution T G upstream_gene_variant BTCA-JP 21 37781715 37781715 single base substitution G A intron_variant BTCA-JP 21 37781715 37781715 single base substitution G A missense_variant V291I 871G>A BTCA-JP 21 37788613 37788613 single base substitution G A downstream_gene_variant BTCA-JP 21 37788613 37788613 single base substitution G A synonymous_variant K543K 1629G>A CLLE-ES 21 37753960 37753960 single base substitution T C upstream_gene_variant CLLE-ES 21 37783066 37783066 single base substitution C A intron_variant COAD-US 21 37759960 37759960 single base substitution G A exon_variant COAD-US 21 37759960 37759960 single base substitution G A missense_variant R64H 191G>A COAD-US 21 37785221 37785221 single base substitution C T exon_variant COAD-US 21 37785221 37785221 single base substitution C T synonymous_variant D367D 1101C>T COAD-US 21 37785464 37785464 single base substitution C T downstream_gene_variant COAD-US 21 37785464 37785464 single base substitution C T synonymous_variant D448D 1344C>T COAD-US 21 37788614 37788614 single base substitution C T downstream_gene_variant COAD-US 21 37788614 37788614 single base substitution C T missense_variant R544W 1630C>T COCA-CN 21 37787538 37787538 single base substitution A C downstream_gene_variant COCA-CN 21 37787538 37787538 single base substitution A C intron_variant EOPC-DE 21 37785511 37785511 single base substitution C T downstream_gene_variant EOPC-DE 21 37785511 37785511 single base substitution C T missense_variant S464L 1391C>T ESAD-UK 21 37755090 37755090 single base substitution C T upstream_gene_variant ESAD-UK 21 37757681 37757694 deletion of <=200bp GCGGCGCGCGGGAA - 5_prime_UTR_variant ESAD-UK 21 37757681 37757694 deletion of <=200bp GCGGCGCGCGGGAA - upstream_gene_variant ESAD-UK 21 37758453 37758453 single base substitution G C exon_variant ESAD-UK 21 37758453 37758453 single base substitution G C missense_variant E7Q 19G>C ESAD-UK 21 37764751 37764751 single base substitution G A intron_variant ESAD-UK 21 37768060 37768060 single base substitution G C intron_variant ESAD-UK 21 37768060 37768060 single base substitution G C upstream_gene_variant ESAD-UK 21 37769579 37769580 deletion of <=200bp AG - intron_variant ESAD-UK 21 37769579 37769580 deletion of <=200bp AG - upstream_gene_variant ESAD-UK 21 37771217 37771217 single base substitution T A downstream_gene_variant ESAD-UK 21 37771217 37771217 single base substitution T A intron_variant ESAD-UK 21 37771217 37771217 single base substitution T A upstream_gene_variant ESAD-UK 21 37773932 37773932 single base substitution T C downstream_gene_variant ESAD-UK 21 37773932 37773932 single base substitution T C intron_variant ESAD-UK 21 37778595 37778595 deletion of <=200bp T - intron_variant ESAD-UK 21 37779949 37779949 single base substitution A G intron_variant ESAD-UK 21 37780314 37780314 insertion of <=200bp - AAG intron_variant ESAD-UK 21 37783007 37783007 deletion of <=200bp G - intron_variant ESAD-UK 21 37785246 37785246 single base substitution G C exon_variant ESAD-UK 21 37785246 37785246 single base substitution G C missense_variant E376Q 1126G>C ESAD-UK 21 37785281 37785281 single base substitution G A downstream_gene_variant ESAD-UK 21 37785281 37785281 single base substitution G A synonymous_variant K387K 1161G>A ESAD-UK 21 37788710 37788710 single base substitution G A 3_prime_UTR_variant ESAD-UK 21 37788710 37788710 single base substitution G A downstream_gene_variant ESAD-UK 21 37790402 37790402 single base substitution C T 3_prime_UTR_variant ESAD-UK 21 37790784 37790784 single base substitution C T 3_prime_UTR_variant ESAD-UK 21 37793394 37793395 deletion of <=200bp TG - downstream_gene_variant ESAD-UK 21 37795224 37795224 single base substitution C T downstream_gene_variant ESAD-UK 21 37795951 37795951 single base substitution C T downstream_gene_variant KIRC-US 21 37783835 37783835 single base substitution A G exon_variant KIRC-US 21 37783835 37783835 single base substitution A G missense_variant T332A 994A>G KIRC-US 21 37785583 37785583 single base substitution C G downstream_gene_variant KIRC-US 21 37785583 37785583 single base substitution C G missense_variant T488R 1463C>G LAML-KR 21 37783967 37783967 single base substitution C T intron_variant LGG-US 21 37775114 37775114 single base substitution G C downstream_gene_variant LGG-US 21 37775114 37775114 single base substitution G C exon_variant LGG-US 21 37775114 37775114 single base substitution G C missense_variant S241T 722G>C LICA-FR 21 37752935 37752935 single base substitution A G upstream_gene_variant LICA-FR 21 37758474 37758474 single base substitution G A exon_variant LICA-FR 21 37758474 37758474 single base substitution G A missense_variant E14K 40G>A LICA-FR 21 37778615 37778615 single base substitution C G intron_variant LICA-FR 21 37779599 37779599 deletion of <=200bp A - intron_variant LICA-FR 21 37781128 37781128 single base substitution G A intron_variant LICA-FR 21 37781128 37781128 single base substitution G A missense_variant R276K 827G>A LIHC-US 21 37785409 37785409 single base substitution C A downstream_gene_variant LIHC-US 21 37785409 37785409 single base substitution C A missense_variant P430H 1289C>A LINC-JP 21 37753433 37753433 single base substitution C T upstream_gene_variant LINC-JP 21 37772132 37772132 single base substitution C G downstream_gene_variant LINC-JP 21 37772132 37772132 single base substitution C G intron_variant LINC-JP 21 37775113 37775113 single base substitution A G downstream_gene_variant LINC-JP 21 37775113 37775113 single base substitution A G exon_variant LINC-JP 21 37775113 37775113 single base substitution A G missense_variant S241G 721A>G LINC-JP 21 37782169 37782169 single base substitution C T intron_variant LIRI-JP 21 37754661 37754661 single base substitution A G upstream_gene_variant LIRI-JP 21 37756452 37756452 single base substitution T C upstream_gene_variant LIRI-JP 21 37757099 37757099 single base substitution T C upstream_gene_variant LIRI-JP 21 37764332 37764332 single base substitution A G intron_variant LIRI-JP 21 37767290 37767290 single base substitution A G intron_variant LIRI-JP 21 37767290 37767290 single base substitution A G upstream_gene_variant LIRI-JP 21 37772708 37772708 single base substitution G A downstream_gene_variant LIRI-JP 21 37772708 37772708 single base substitution G A intron_variant LIRI-JP 21 37772887 37772887 single base substitution T C downstream_gene_variant LIRI-JP 21 37772887 37772887 single base substitution T C intron_variant LIRI-JP 21 37773559 37773559 single base substitution C G downstream_gene_variant LIRI-JP 21 37773559 37773559 single base substitution C G intron_variant LIRI-JP 21 37774226 37774226 single base substitution A G downstream_gene_variant LIRI-JP 21 37774226 37774226 single base substitution A G intron_variant LIRI-JP 21 37774933 37774933 single base substitution C A downstream_gene_variant LIRI-JP 21 37774933 37774933 single base substitution C A intron_variant LIRI-JP 21 37775150 37775151 deletion of <=200bp GT - downstream_gene_variant LIRI-JP 21 37775150 37775151 deletion of <=200bp GT - splice_donor_variant LIRI-JP 21 37779057 37779057 single base substitution T C intron_variant LIRI-JP 21 37779833 37779833 single base substitution G A intron_variant LIRI-JP 21 37781006 37781006 single base substitution G C intron_variant LIRI-JP 21 37781194 37781194 single base substitution C A intron_variant LIRI-JP 21 37782445 37782445 single base substitution G T intron_variant LIRI-JP 21 37783175 37783175 single base substitution T C intron_variant LIRI-JP 21 37784510 37784510 single base substitution G T intron_variant LIRI-JP 21 37787661 37787661 single base substitution C A downstream_gene_variant LIRI-JP 21 37787661 37787661 single base substitution C A missense_variant T521N 1562C>A LIRI-JP 21 37789026 37789026 single base substitution A G 3_prime_UTR_variant LIRI-JP 21 37789026 37789026 single base substitution A G downstream_gene_variant LIRI-JP 21 37789156 37789156 single base substitution C T 3_prime_UTR_variant LIRI-JP 21 37789156 37789156 single base substitution C T downstream_gene_variant LIRI-JP 21 37792056 37792056 single base substitution C T downstream_gene_variant LIRI-JP 21 37792147 37792147 insertion of <=200bp - GACA downstream_gene_variant LIRI-JP 21 37792611 37792611 single base substitution A G downstream_gene_variant LIRI-JP 21 37793889 37793889 single base substitution G C downstream_gene_variant LIRI-JP 21 37794819 37794819 single base substitution T C downstream_gene_variant LIRI-JP 21 37794969 37794969 single base substitution T C downstream_gene_variant LIRI-JP 21 37795272 37795272 single base substitution T C downstream_gene_variant LUSC-KR 21 37753327 37753327 single base substitution G T upstream_gene_variant LUSC-KR 21 37753329 37753329 single base substitution G T upstream_gene_variant LUSC-KR 21 37754979 37754979 single base substitution A T upstream_gene_variant LUSC-KR 21 37759539 37759539 single base substitution G T intron_variant LUSC-KR 21 37763145 37763145 single base substitution G T intron_variant LUSC-KR 21 37763785 37763785 single base substitution T A intron_variant LUSC-KR 21 37768983 37768983 single base substitution A C intron_variant LUSC-KR 21 37768983 37768983 single base substitution A C upstream_gene_variant LUSC-KR 21 37772306 37772306 single base substitution A G downstream_gene_variant LUSC-KR 21 37772306 37772306 single base substitution A G intron_variant LUSC-KR 21 37777195 37777195 single base substitution C T intron_variant LUSC-KR 21 37782006 37782006 single base substitution G A intron_variant LUSC-KR 21 37782952 37782952 single base substitution A T intron_variant LUSC-US 21 37763859 37763859 single base substitution C A exon_variant LUSC-US 21 37763859 37763859 single base substitution C A synonymous_variant I90I 270C>A LUSC-US 21 37775112 37775112 single base substitution G T downstream_gene_variant LUSC-US 21 37775112 37775112 single base substitution G T exon_variant LUSC-US 21 37775112 37775112 single base substitution G T synonymous_variant L240L 720G>T LUSC-US 21 37788602 37788602 single base substitution C T downstream_gene_variant LUSC-US 21 37788602 37788602 single base substitution C T missense_variant P540S 1618C>T MALY-DE 21 37752764 37752764 single base substitution T G upstream_gene_variant MALY-DE 21 37755479 37755479 single base substitution C T upstream_gene_variant MALY-DE 21 37763381 37763381 single base substitution C G intron_variant MALY-DE 21 37779752 37779752 single base substitution C A intron_variant MALY-DE 21 37790395 37790395 single base substitution C T 3_prime_UTR_variant MELA-AU 21 37753051 37753051 single base substitution C T upstream_gene_variant MELA-AU 21 37753144 37753145 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 21 37753733 37753733 single base substitution T A upstream_gene_variant MELA-AU 21 37753785 37753785 single base substitution T C upstream_gene_variant MELA-AU 21 37756359 37756360 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 21 37757347 37757347 single base substitution C T upstream_gene_variant MELA-AU 21 37757612 37757612 single base substitution G A upstream_gene_variant MELA-AU 21 37757625 37757625 single base substitution G A upstream_gene_variant MELA-AU 21 37757634 37757634 single base substitution G A upstream_gene_variant MELA-AU 21 37757637 37757638 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 21 37757643 37757643 single base substitution G A upstream_gene_variant MELA-AU 21 37757657 37757657 single base substitution C T upstream_gene_variant MELA-AU 21 37757669 37757670 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 21 37757676 37757677 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 21 37757676 37757677 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 21 37757692 37757692 single base substitution G A 5_prime_UTR_variant MELA-AU 21 37757692 37757692 single base substitution G A upstream_gene_variant MELA-AU 21 37758022 37758022 single base substitution C T intron_variant MELA-AU 21 37758022 37758022 single base substitution C T upstream_gene_variant MELA-AU 21 37758824 37758824 single base substitution C T intron_variant MELA-AU 21 37759046 37759046 single base substitution C T intron_variant MELA-AU 21 37759143 37759143 single base substitution C G intron_variant MELA-AU 21 37759237 37759237 single base substitution C T intron_variant MELA-AU 21 37759641 37759641 single base substitution C T intron_variant MELA-AU 21 37760378 37760378 single base substitution C T intron_variant MELA-AU 21 37760763 37760764 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 21 37760782 37760782 single base substitution T A intron_variant MELA-AU 21 37761060 37761060 single base substitution C T intron_variant MELA-AU 21 37761414 37761414 single base substitution C T intron_variant MELA-AU 21 37762326 37762326 single base substitution C T intron_variant MELA-AU 21 37763681 37763681 single base substitution G A intron_variant MELA-AU 21 37763741 37763741 single base substitution G A intron_variant MELA-AU 21 37764027 37764027 single base substitution T C intron_variant MELA-AU 21 37764676 37764676 single base substitution C T intron_variant MELA-AU 21 37764938 37764938 single base substitution C T intron_variant MELA-AU 21 37765186 37765186 single base substitution G A intron_variant MELA-AU 21 37765278 37765278 single base substitution C T intron_variant MELA-AU 21 37766153 37766153 single base substitution C T intron_variant MELA-AU 21 37767524 37767524 single base substitution C A intron_variant MELA-AU 21 37767524 37767524 single base substitution C A upstream_gene_variant MELA-AU 21 37768331 37768331 single base substitution C T intron_variant MELA-AU 21 37768331 37768331 single base substitution C T upstream_gene_variant MELA-AU 21 37768382 37768382 single base substitution T G intron_variant MELA-AU 21 37768382 37768382 single base substitution T G upstream_gene_variant MELA-AU 21 37769312 37769312 single base substitution C T intron_variant MELA-AU 21 37769312 37769312 single base substitution C T upstream_gene_variant MELA-AU 21 37769419 37769419 single base substitution C A intron_variant MELA-AU 21 37769419 37769419 single base substitution C A upstream_gene_variant MELA-AU 21 37769451 37769451 single base substitution C T intron_variant MELA-AU 21 37769451 37769451 single base substitution C T upstream_gene_variant MELA-AU 21 37771629 37771629 single base substitution C T downstream_gene_variant MELA-AU 21 37771629 37771629 single base substitution C T intron_variant MELA-AU 21 37771629 37771629 single base substitution C T upstream_gene_variant MELA-AU 21 37772824 37772824 single base substitution C T downstream_gene_variant MELA-AU 21 37772824 37772824 single base substitution C T intron_variant MELA-AU 21 37773187 37773187 single base substitution T A downstream_gene_variant MELA-AU 21 37773187 37773187 single base substitution T A intron_variant MELA-AU 21 37774450 37774450 single base substitution T G downstream_gene_variant MELA-AU 21 37774450 37774450 single base substitution T G intron_variant MELA-AU 21 37774882 37774882 single base substitution C T downstream_gene_variant MELA-AU 21 37774882 37774882 single base substitution C T intron_variant MELA-AU 21 37775321 37775321 single base substitution C T downstream_gene_variant MELA-AU 21 37775321 37775321 single base substitution C T intron_variant MELA-AU 21 37775797 37775797 single base substitution C T intron_variant MELA-AU 21 37776957 37776957 single base substitution C T intron_variant MELA-AU 21 37777546 37777546 single base substitution G A intron_variant MELA-AU 21 37777700 37777700 single base substitution C T intron_variant MELA-AU 21 37778201 37778201 single base substitution G A intron_variant MELA-AU 21 37778591 37778591 single base substitution C T intron_variant MELA-AU 21 37781114 37781114 single base substitution G A intron_variant MELA-AU 21 37781114 37781114 single base substitution G A synonymous_variant R271R 813G>A MELA-AU 21 37781553 37781553 single base substitution C T intron_variant MELA-AU 21 37782515 37782515 single base substitution C T intron_variant MELA-AU 21 37782852 37782852 single base substitution T C intron_variant MELA-AU 21 37782922 37782922 single base substitution C T intron_variant MELA-AU 21 37783128 37783128 single base substitution T A intron_variant MELA-AU 21 37783757 37783757 single base substitution C T splice_region_variant MELA-AU 21 37784403 37784403 single base substitution C T intron_variant MELA-AU 21 37784641 37784641 single base substitution C T intron_variant MELA-AU 21 37785349 37785349 single base substitution C T downstream_gene_variant MELA-AU 21 37785349 37785349 single base substitution C T missense_variant S410L 1229C>T MELA-AU 21 37785383 37785383 single base substitution C T downstream_gene_variant MELA-AU 21 37785383 37785383 single base substitution C T synonymous_variant A421A 1263C>T MELA-AU 21 37785496 37785496 single base substitution C T downstream_gene_variant MELA-AU 21 37785496 37785496 single base substitution C T missense_variant P459L 1376C>T MELA-AU 21 37785981 37785981 single base substitution C A downstream_gene_variant MELA-AU 21 37785981 37785981 single base substitution C A intron_variant MELA-AU 21 37785991 37785991 single base substitution G A downstream_gene_variant MELA-AU 21 37785991 37785991 single base substitution G A intron_variant MELA-AU 21 37786314 37786314 single base substitution C T downstream_gene_variant MELA-AU 21 37786314 37786314 single base substitution C T intron_variant MELA-AU 21 37786500 37786500 single base substitution C T downstream_gene_variant MELA-AU 21 37786500 37786500 single base substitution C T intron_variant MELA-AU 21 37786533 37786533 single base substitution C T downstream_gene_variant MELA-AU 21 37786533 37786533 single base substitution C T intron_variant MELA-AU 21 37787248 37787248 single base substitution C T downstream_gene_variant MELA-AU 21 37787248 37787248 single base substitution C T intron_variant MELA-AU 21 37787425 37787425 single base substitution C T downstream_gene_variant MELA-AU 21 37787425 37787425 single base substitution C T intron_variant MELA-AU 21 37787723 37787723 single base substitution G A downstream_gene_variant MELA-AU 21 37787723 37787723 single base substitution G A intron_variant MELA-AU 21 37789207 37789207 single base substitution C T 3_prime_UTR_variant MELA-AU 21 37789207 37789207 single base substitution C T downstream_gene_variant MELA-AU 21 37789879 37789879 single base substitution C T 3_prime_UTR_variant MELA-AU 21 37789879 37789879 single base substitution C T downstream_gene_variant MELA-AU 21 37790117 37790117 single base substitution C T 3_prime_UTR_variant MELA-AU 21 37790117 37790117 single base substitution C T downstream_gene_variant MELA-AU 21 37790135 37790135 single base substitution C T 3_prime_UTR_variant MELA-AU 21 37790135 37790135 single base substitution C T downstream_gene_variant MELA-AU 21 37790147 37790147 single base substitution T C 3_prime_UTR_variant MELA-AU 21 37790147 37790147 single base substitution T C downstream_gene_variant MELA-AU 21 37790333 37790333 single base substitution G A 3_prime_UTR_variant MELA-AU 21 37790804 37790804 single base substitution C T 3_prime_UTR_variant MELA-AU 21 37790973 37790973 single base substitution C T 3_prime_UTR_variant MELA-AU 21 37791196 37791196 single base substitution C G 3_prime_UTR_variant MELA-AU 21 37791225 37791225 deletion of <=200bp G - 3_prime_UTR_variant MELA-AU 21 37791269 37791269 single base substitution C T 3_prime_UTR_variant MELA-AU 21 37791907 37791907 single base substitution C T downstream_gene_variant MELA-AU 21 37792069 37792069 single base substitution C T downstream_gene_variant MELA-AU 21 37793710 37793710 single base substitution T C downstream_gene_variant MELA-AU 21 37793877 37793877 single base substitution C T downstream_gene_variant MELA-AU 21 37793895 37793895 single base substitution C T downstream_gene_variant MELA-AU 21 37794086 37794086 single base substitution C T downstream_gene_variant MELA-AU 21 37794845 37794845 single base substitution C T downstream_gene_variant MELA-AU 21 37794846 37794846 single base substitution C T downstream_gene_variant MELA-AU 21 37795197 37795197 single base substitution C T downstream_gene_variant MELA-AU 21 37795860 37795860 single base substitution C T downstream_gene_variant MELA-AU 21 37795952 37795953 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 21 37795963 37795963 single base substitution C T downstream_gene_variant ORCA-IN 21 37754917 37754917 single base substitution C A upstream_gene_variant ORCA-IN 21 37785177 37785177 single base substitution C T exon_variant ORCA-IN 21 37785177 37785177 single base substitution C T splice_region_variant ORCA-IN 21 37790757 37790757 single base substitution G A 3_prime_UTR_variant OV-AU 21 37756071 37756071 single base substitution C T upstream_gene_variant OV-AU 21 37758779 37758779 single base substitution G C intron_variant OV-AU 21 37784563 37784563 single base substitution A T intron_variant OV-AU 21 37784950 37784950 single base substitution G A intron_variant OV-AU 21 37788599 37788599 single base substitution C T downstream_gene_variant OV-AU 21 37788599 37788599 single base substitution C T missense_variant P539S 1615C>T OV-AU 21 37794817 37794817 single base substitution G A downstream_gene_variant OV-US 21 37758546 37758546 single base substitution G T exon_variant OV-US 21 37758546 37758546 single base substitution G T missense_variant D38Y 112G>T PACA-AU 21 37760291 37760291 single base substitution G T intron_variant PACA-AU 21 37764583 37764583 single base substitution C G intron_variant PACA-AU 21 37776655 37776655 single base substitution C T intron_variant PACA-AU 21 37786730 37786730 single base substitution C T downstream_gene_variant PACA-AU 21 37786730 37786730 single base substitution C T intron_variant PACA-AU 21 37788020 37788020 single base substitution G A downstream_gene_variant PACA-AU 21 37788020 37788020 single base substitution G A intron_variant PACA-AU 21 37788344 37788344 single base substitution G A downstream_gene_variant PACA-AU 21 37788344 37788344 single base substitution G A intron_variant PACA-CA 21 37752890 37752890 single base substitution A T upstream_gene_variant PACA-CA 21 37754557 37754557 single base substitution T C upstream_gene_variant PACA-CA 21 37758491 37758491 deletion of <=200bp G - exon_variant PACA-CA 21 37758491 37758491 deletion of <=200bp G - frameshift_variant L19 PACA-CA 21 37760067 37760067 single base substitution G C intron_variant PACA-CA 21 37760073 37760073 single base substitution T A intron_variant PACA-CA 21 37760291 37760291 single base substitution G T intron_variant PACA-CA 21 37763902 37763902 single base substitution G A exon_variant PACA-CA 21 37763902 37763902 single base substitution G A missense_variant A105T 313G>A PACA-CA 21 37766904 37766904 single base substitution C T exon_variant PACA-CA 21 37766904 37766904 single base substitution C T missense_variant S146F 437C>T PACA-CA 21 37766904 37766904 single base substitution C T upstream_gene_variant PACA-CA 21 37768963 37768963 single base substitution A G intron_variant PACA-CA 21 37768963 37768963 single base substitution A G upstream_gene_variant PACA-CA 21 37772223 37772223 single base substitution T C downstream_gene_variant PACA-CA 21 37772223 37772223 single base substitution T C intron_variant PACA-CA 21 37774601 37774601 single base substitution C T downstream_gene_variant PACA-CA 21 37774601 37774601 single base substitution C T intron_variant PACA-CA 21 37779300 37779300 single base substitution C A intron_variant PACA-CA 21 37785988 37785988 single base substitution G T downstream_gene_variant PACA-CA 21 37785988 37785988 single base substitution G T intron_variant PACA-CA 21 37786655 37786655 single base substitution G A downstream_gene_variant PACA-CA 21 37786655 37786655 single base substitution G A intron_variant PACA-CA 21 37787273 37787273 single base substitution T C downstream_gene_variant PACA-CA 21 37787273 37787273 single base substitution T C intron_variant PACA-CA 21 37789595 37789595 single base substitution C T 3_prime_UTR_variant PACA-CA 21 37789595 37789595 single base substitution C T downstream_gene_variant PACA-CA 21 37790207 37790207 single base substitution T G 3_prime_UTR_variant PACA-CA 21 37790207 37790207 single base substitution T G downstream_gene_variant PACA-CA 21 37795841 37795841 single base substitution C T downstream_gene_variant PAEN-AU 21 37790280 37790280 single base substitution G T 3_prime_UTR_variant PAEN-IT 21 37766032 37766032 single base substitution G A intron_variant PBCA-DE 21 37756040 37756040 single base substitution G A upstream_gene_variant PBCA-DE 21 37762120 37762120 single base substitution G C intron_variant PBCA-DE 21 37764185 37764185 insertion of <=200bp - CATG intron_variant PBCA-DE 21 37765448 37765448 single base substitution G T intron_variant PRAD-CA 21 37773932 37773932 single base substitution T C downstream_gene_variant PRAD-CA 21 37773932 37773932 single base substitution T C intron_variant PRAD-CA 21 37788060 37788060 single base substitution C T downstream_gene_variant PRAD-CA 21 37788060 37788060 single base substitution C T intron_variant PRAD-UK 21 37755017 37755019 deletion of <=200bp TTT - upstream_gene_variant PRAD-UK 21 37761363 37761363 single base substitution C T intron_variant PRAD-UK 21 37770261 37770261 single base substitution A G exon_variant PRAD-UK 21 37770261 37770261 single base substitution A G intron_variant PRAD-UK 21 37770261 37770261 single base substitution A G upstream_gene_variant PRAD-UK 21 37779674 37779674 insertion of <=200bp - A intron_variant PRAD-UK 21 37790100 37790100 single base substitution T C 3_prime_UTR_variant PRAD-UK 21 37790100 37790100 single base substitution T C downstream_gene_variant PRAD-UK 21 37790101 37790101 single base substitution A T 3_prime_UTR_variant PRAD-UK 21 37790101 37790101 single base substitution A T downstream_gene_variant RECA-EU 21 37755651 37755651 single base substitution C T upstream_gene_variant RECA-EU 21 37761371 37761371 single base substitution C A intron_variant RECA-EU 21 37766032 37766032 single base substitution G A intron_variant RECA-EU 21 37768281 37768281 single base substitution G A intron_variant RECA-EU 21 37768281 37768281 single base substitution G A upstream_gene_variant RECA-EU 21 37771323 37771323 single base substitution G C downstream_gene_variant RECA-EU 21 37771323 37771323 single base substitution G C intron_variant RECA-EU 21 37771323 37771323 single base substitution G C upstream_gene_variant RECA-EU 21 37789070 37789070 single base substitution G A 3_prime_UTR_variant RECA-EU 21 37789070 37789070 single base substitution G A downstream_gene_variant RECA-EU 21 37790178 37790178 single base substitution C T 3_prime_UTR_variant RECA-EU 21 37790178 37790178 single base substitution C T downstream_gene_variant SKCA-BR 21 37754846 37754846 single base substitution T C upstream_gene_variant SKCA-BR 21 37755385 37755386 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 21 37756853 37756853 single base substitution A G upstream_gene_variant SKCA-BR 21 37757648 37757648 single base substitution C T upstream_gene_variant SKCA-BR 21 37757717 37757717 single base substitution T G 5_prime_UTR_variant SKCA-BR 21 37757717 37757717 single base substitution T G upstream_gene_variant SKCA-BR 21 37758055 37758055 single base substitution G C intron_variant SKCA-BR 21 37758055 37758055 single base substitution G C upstream_gene_variant SKCA-BR 21 37760766 37760768 deletion of <=200bp GTT - intron_variant SKCA-BR 21 37768300 37768300 insertion of <=200bp - GT intron_variant SKCA-BR 21 37768300 37768300 insertion of <=200bp - GT upstream_gene_variant SKCA-BR 21 37768628 37768628 single base substitution G A intron_variant SKCA-BR 21 37768628 37768628 single base substitution G A upstream_gene_variant SKCA-BR 21 37769882 37769882 single base substitution C T intron_variant SKCA-BR 21 37769882 37769882 single base substitution C T upstream_gene_variant SKCA-BR 21 37770888 37770888 single base substitution C T downstream_gene_variant SKCA-BR 21 37770888 37770888 single base substitution C T intron_variant SKCA-BR 21 37770888 37770888 single base substitution C T upstream_gene_variant SKCA-BR 21 37776394 37776394 insertion of <=200bp - CT intron_variant SKCA-BR 21 37777340 37777345 deletion of <=200bp CGCCCA - intron_variant SKCA-BR 21 37784215 37784215 single base substitution T G intron_variant SKCA-BR 21 37787248 37787248 single base substitution C T downstream_gene_variant SKCA-BR 21 37787248 37787248 single base substitution C T intron_variant SKCA-BR 21 37788482 37788482 single base substitution C T downstream_gene_variant SKCA-BR 21 37788482 37788482 single base substitution C T intron_variant SKCA-BR 21 37788959 37788959 single base substitution C T 3_prime_UTR_variant SKCA-BR 21 37788959 37788959 single base substitution C T downstream_gene_variant SKCA-BR 21 37795289 37795289 single base substitution C G downstream_gene_variant SKCM-US 21 37785199 37785199 single base substitution T G exon_variant SKCM-US 21 37785199 37785199 single base substitution T G missense_variant F360C 1079T>G SKCM-US 21 37785272 37785272 single base substitution G A downstream_gene_variant SKCM-US 21 37785272 37785272 single base substitution G A synonymous_variant L384L 1152G>A SKCM-US 21 37785495 37785495 single base substitution C T downstream_gene_variant SKCM-US 21 37785495 37785495 single base substitution C T missense_variant P459S 1375C>T SKCM-US 21 37785496 37785496 single base substitution C T downstream_gene_variant SKCM-US 21 37785496 37785496 single base substitution C T missense_variant P459L 1376C>T SKCM-US 21 37788600 37788600 single base substitution C T downstream_gene_variant SKCM-US 21 37788600 37788600 single base substitution C T missense_variant P539L 1616C>T STAD-US 21 37759988 37759988 single base substitution T C exon_variant STAD-US 21 37759988 37759988 single base substitution T C synonymous_variant R73R 219T>C STAD-US 21 37781130 37781130 single base substitution T C intron_variant STAD-US 21 37781130 37781130 single base substitution T C splice_donor_variant STAD-US 21 37788576 37788576 single base substitution C T downstream_gene_variant STAD-US 21 37788576 37788576 single base substitution C T missense_variant T531M 1592C>T THCA-SA 21 37759957 37759957 single base substitution C T exon_variant THCA-SA 21 37759957 37759957 single base substitution C T missense_variant A63V 188C>T UCEC-US 21 37759895 37759895 single base substitution G T splice_acceptor_variant UCEC-US 21 37759959 37759959 single base substitution C T exon_variant UCEC-US 21 37759959 37759959 single base substitution C T missense_variant R64C 190C>T UCEC-US 21 37769720 37769720 single base substitution G T exon_variant UCEC-US 21 37769720 37769720 single base substitution G T missense_variant K163N 489G>T UCEC-US 21 37769720 37769720 single base substitution G T upstream_gene_variant UCEC-US 21 37781718 37781718 single base substitution C T intron_variant UCEC-US 21 37781718 37781718 single base substitution C T missense_variant R292C 874C>T UCEC-US 21 37783763 37783763 single base substitution G A missense_variant V308M 922G>A UCEC-US 21 37783763 37783763 single base substitution G A splice_region_variant UCEC-US 21 37785268 37785268 single base substitution C A downstream_gene_variant UCEC-US 21 37785268 37785268 single base substitution C A missense_variant P383H 1148C>A UCEC-US 21 37785304 37785304 single base substitution C A downstream_gene_variant UCEC-US 21 37785304 37785304 single base substitution C A missense_variant P395H 1184C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand C135 COSM4618103 c.98C>T p.A33V Substitution - Missense 21:36386234-36386234 + TCGA-HU-A4GP-01 COSM4013618 c.1336G>A p.G446S Substitution - Missense 10:28058566-28058566 - HCC136T COSM5817162 c.641T>G p.F214C Substitution - Missense 10:28120643-28120643 - C086 COSM5528618 c.1511C>T p.P504L Substitution - Missense 21:36415312-36415312 + TCGA-AP-A051-01 COSM917495 c.1240G>T p.G414C Substitution - Missense 10:28059708-28059708 - T3090 COSM3722570 c.567C>T p.N189N Substitution - coding silent 10:28124079-28124079 - BN24T COSM1603377 c.835G>T p.A279S Substitution - Missense 10:28120246-28120246 - P48 COSM328772 c.1048A>T p.S350C Substitution - Missense 21:36411591-36411591 + TCGA-D1-A17Q-01 COSM917502 c.483G>A p.A161A Substitution - coding silent 10:28125056-28125056 - TCGA-ER-A193-06 COSM3437073 c.1237G>A p.D413N Substitution - Missense 10:28059711-28059711 - TCGA-ER-A19J-06 COSM3437082 c.787C>T p.Q263* Substitution - Nonsense 10:28120294-28120294 - TCGA-AZ-4682-01 COSM1414002 c.1101C>T p.D367D Substitution - coding silent 21:36412923-36412923 + OSCC-GB_01160111 COSM5956040 c.1062-5C>T p.? Unknown 21:36412879-36412879 + TCGA-HW-8319-01 COSM3967029 c.1431A>G p.L477L Substitution - coding silent 10:28056600-28056600 - T98G COSM2134749 c.1636G>A p.D546N Substitution - Missense 10:28054160-28054160 - TCGA-GF-A6C8-06 COSM3912067 c.1375C>T p.P459S Substitution - Missense 21:36413197-36413197 + TCGA-51-4080-01 COSM684570 c.1242T>A p.G414G Substitution - coding silent 10:28059706-28059706 - TCGA-A8-A0A6-01 COSM3841872 c.284T>G p.V95G Substitution - Missense 21:36391575-36391575 + TCGA-AX-A05S-01 COSM917499 c.1082G>A p.R361Q Substitution - Missense 10:28089712-28089712 - YUKAT COSM3437093 c.400G>A p.E134K Substitution - Missense 10:28131607-28131607 - Pat_06_A COSM5858594 c.476G>A p.S159N Substitution - Missense 21:36394645-36394645 + TCGA-66-2795-01 COSM684573 c.1466C>A p.P489Q Substitution - Missense 10:28056565-28056565 - SB_07 COSM5753216 c.370_371insC p.P125fs*4 Insertion - Frameshift 10:28131636-28131637 - YUMER COSM1713969 c.471T>G p.D157E Substitution - Missense 21:36394640-36394640 + CT-TC COSM1030538 c.922G>A p.V308M Substitution - Missense 21:36411465-36411465 + TCGA-F1-6177-01 COSM3437076 c.1063G>A p.E355K Substitution - Missense 10:28089731-28089731 - ASHPC_0023_Pa_P COSM4806711 c.313G>A p.A105T Substitution - Missense 21:36391604-36391604 + TCGA-B2-3924-01 COSM465579 c.1055C>A p.P352H Substitution - Missense 10:28089739-28089739 - TCGA-EE-A29E-06 COSM3437097 c.380C>T p.P127L Substitution - Missense 10:28131627-28131627 - TCGA-AP-A051-01 COSM917497 c.1204+1G>A p.? Unknown 10:28069771-28069771 - BD121T COSM3437076 c.1063G>A p.E355K Substitution - Missense 10:28089731-28089731 - TCGA-13-1412-01 COSM75455 c.888G>C p.R296S Substitution - Missense 10:28119715-28119715 - TCGA-CG-4444-01 COSM4013619 c.1219A>T p.R407* Substitution - Nonsense 10:28059729-28059729 - TCGA-EE-A2GU-06 COSM3437084 c.751G>A p.E251K Substitution - Missense 10:28120330-28120330 - CHC892T COSM4797347 c.686G>A p.G229D Substitution - Missense 10:28120598-28120598 - TCGA-A5-A0GB-01 COSM917503 c.422G>A p.R141H Substitution - Missense 10:28131585-28131585 - TCGA-AG-3608-01 COSM288114 c.18G>A p.T6T Substitution - coding silent 10:28238587-28238587 - TCGA-A5-A0R8-01 COSM917494 c.1407+1G>A p.? Unknown 10:28058494-28058494 - TCGA-EB-A24D-01 COSM3437085 c.742C>T p.P248S Substitution - Missense 10:28120339-28120339 - TCGA-AP-A0LM-01 COSM917499 c.1082G>A p.R361Q Substitution - Missense 10:28089712-28089712 - SMS-CTR COSM1030538 c.922G>A p.V308M Substitution - Missense 21:36411465-36411465 + TCGA-BT-A3PJ-01 COSM3790720 c.699C>G p.I233M Substitution - Missense 10:28120382-28120382 - ESCC_BICR_027T COSM5443123 c.1520G>C p.R507T Substitution - Missense 10:28056511-28056511 - TCGA-ER-A199-06 COSM3437081 c.879C>T p.F293F Substitution - coding silent 10:28120202-28120202 - TCGA-E9-A1N4-01 COSM1483929 c.591A>G p.V197V Substitution - coding silent 21:36399533-36399533 + TCGA-EE-A29A-06 COSM3437070 c.1320T>A p.Y440* Substitution - Nonsense 10:28058582-28058582 - TCGA-D3-A5GS-06 COSM3437086 c.706C>T p.L236F Substitution - Missense 10:28120375-28120375 - TCGA-BR-6452-01 COSM4013621 c.1036T>C p.Y346H Substitution - Missense 10:28089758-28089758 - TCGA-66-2759-01 COSM684568 c.364G>T p.V122L Substitution - Missense 10:28131643-28131643 - CHC892T COSM4797347 c.686G>A p.G229D Substitution - Missense 10:28120598-28120598 - TCGA-04-1644-01 COSM1321392 c.977T>G p.L326R Substitution - Missense 10:28089817-28089817 - TCGA-BS-A0UF-01 COSM106976 c.874C>T p.R292C Substitution - Missense 21:36409420-36409420 + 2492723 COSM5724009 c.1306G>A p.E436K Substitution - Missense 10:28058596-28058596 - 587220 COSM1200934 c.1295C>T p.T432M Substitution - Missense 21:36413117-36413117 + GC8_T COSM146915 c.1110C>T p.L370L Substitution - coding silent 10:28089684-28089684 - YUPAT COSM1702219 c.364G>A p.V122M Substitution - Missense 10:28131643-28131643 - YULETA COSM3437077 c.1039G>A p.D347N Substitution - Missense 10:28089755-28089755 - 1_PRE-TREATMENT COSM1719525 c.832G>A p.E278K Substitution - Missense 10:28120249-28120249 - TCGA-27-1833-01 COSM3397084 c.1491A>G p.T497T Substitution - coding silent 10:28056540-28056540 - S02403 COSM5700330 c.1565A>T p.Q522L Substitution - Missense 10:28054231-28054231 - 2521262 COSM5892086 c.157-4C>T p.? Unknown 10:28150063-28150063 - TCGA-C5-A7CJ-01 COSM4821354 c.316-2A>G p.? Unknown 10:28131693-28131693 - TCGA-EE-A2GC-06 COSM3437075 c.1075C>T p.P359S Substitution - Missense 10:28089719-28089719 - N508T COSM236161 c.187C>A p.Q63K Substitution - Missense 10:28150029-28150029 - EOPC-03_tumor COSM3716535 c.1391C>T p.S464L Substitution - Missense 21:36413213-36413213 + TCGA-HR-A2OG-01 COSM3550542 c.587G>T p.R196L Substitution - Missense 21:36399529-36399529 + TCGA-EE-A3JD-06 COSM4394802 c.1531G>A p.G511S Substitution - Missense 10:28056500-28056500 - PD13631a COSM5767709 c.616-10C>T p.? Unknown 10:28120678-28120678 - TCGA-BS-A0UF-01 COSM917496 c.1224A>G p.R408R Substitution - coding silent 10:28059724-28059724 - Au1 COSM5596494 c.869C>T p.A290V Substitution - Missense 21:36409415-36409415 + Pat_41_B COSM1713971 c.1256C>T p.T419I Substitution - Missense 21:36413078-36413078 + TCGA-QB-A6FS-06 COSM1702217 c.973C>T p.R325C Substitution - Missense 10:28089821-28089821 - Pat_46_A COSM5836751 c.938C>T p.S313F Substitution - Missense 10:28119665-28119665 - TCGA-22-5480-01 COSM684571 c.1297A>G p.K433E Substitution - Missense 10:28059651-28059651 - YURISA COSM5370543 c.1522G>A p.D508N Substitution - Missense 10:28056509-28056509 - TCGA-ER-A2NC-06 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - MINO COSM917503 c.422G>A p.R141H Substitution - Missense 10:28131585-28131585 - T3262 COSM2134771 c.1050C>T p.D350D Substitution - coding silent 10:28089744-28089744 - CSCC-27-T COSM4464655 c.1345C>T p.P449S Substitution - Missense 21:36413167-36413167 + HCC105T COSM1616051 c.721A>G p.S241G Substitution - Missense 21:36402815-36402815 + CHC892T COSM4794543 c.40G>A p.E14K Substitution - Missense 21:36386176-36386176 + 3_PRE-TREATMENT COSM1723512 c.1376C>T p.P459L Substitution - Missense 21:36413198-36413198 + Pat_14_A COSM5858596 c.1444C>T p.R482W Substitution - Missense 21:36413266-36413266 + TCGA-EI-6507-01 COSM1560814 c.357C>T p.Y119Y Substitution - coding silent 10:28131650-28131650 - 1_RESISTANT COSM1719525 c.832G>A p.E278K Substitution - Missense 10:28120249-28120249 - TCGA-D3-A5GS-06 COSM1239466 c.358G>A p.D120N Substitution - Missense 10:28131649-28131649 - 40M COSM3437081 c.879C>T p.F293F Substitution - coding silent 10:28120202-28120202 - SC_9096 COSM5546797 c.335_344del10 p.Q113fs*7 Deletion - Frameshift 21:36391626-36391635 + TCGA-BR-7851-01 COSM4013620 c.1045G>A p.A349T Substitution - Missense 10:28089749-28089749 - ESCC_153 COSM5645594 c.953-2A>G p.? Unknown 10:28089843-28089843 - 2492722 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - T3236 COSM4703077 c.1369G>T p.A457S Substitution - Missense 10:28058533-28058533 - 113368 COSM325843 c.268A>G p.S90G Substitution - Missense 10:28147530-28147530 - TCGA-BP-5004-01 COSM478563 c.994A>G p.T332A Substitution - Missense 21:36411537-36411537 + TCGA-BR-4361-01 COSM4101479 c.219T>C p.R73R Substitution - coding silent 21:36387690-36387690 + PT35 COSM5914347 c.378-4C>T p.? Unknown 21:36394543-36394543 + PT33 COSM1030536 c.190C>T p.R64C Substitution - Missense 21:36387661-36387661 + TCGA-EE-A29L-06 COSM3437079 c.978T>C p.L326L Substitution - coding silent 10:28089816-28089816 - LUAD-NYU284 COSM373078 c.1540G>T p.V514L Substitution - Missense 21:36415341-36415341 + TCGA-34-5928-01 COSM684572 c.1413G>A p.V471V Substitution - coding silent 10:28056618-28056618 - 2171 COSM5015695 c.377G>A p.R126Q Substitution - Missense 21:36391668-36391668 + TCGA-D1-A15X-01 COSM917498 c.1192G>A p.V398M Substitution - Missense 10:28069784-28069784 - 96T COSM106976 c.874C>T p.R292C Substitution - Missense 21:36409420-36409420 + TCGA-BS-A0UA-01 COSM917499 c.1082G>A p.R361Q Substitution - Missense 10:28089712-28089712 - TCGA-EB-A44O-01 COSM3437067 c.1541A>G p.K514R Substitution - Missense 10:28056490-28056490 - HCC153T COSM5823238 c.615+1G>T p.? Unknown 10:28124030-28124030 - T3306 COSM4671917 c.712C>T p.R238C Substitution - Missense 21:36402806-36402806 + TCGA-AP-A0LM-01 COSM917506 c.194C>T p.P65L Substitution - Missense 10:28150022-28150022 - PTC-28C COSM4134918 c.54C>T p.S18S Substitution - coding silent 21:36386190-36386190 + TCGA-39-5035-01 COSM684569 c.1208C>T p.T403I Substitution - Missense 10:28059740-28059740 - 2492721 COSM5724389 c.248C>T p.S83L Substitution - Missense 21:36387719-36387719 + TCGA-FS-A1Z3-06 COSM3437066 c.1594G>A p.E532K Substitution - Missense 10:28054202-28054202 - TCGA-EE-A20C-06 COSM3437083 c.772A>C p.K258Q Substitution - Missense 10:28120309-28120309 - TCGA-BR-6452-01 COSM4101480 c.827+2T>C p.? Unknown 21:36408832-36408832 + LIM2099 COSM4641160 c.1405C>G p.L469V Substitution - Missense 21:36413227-36413227 + 2492723 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - BD179T COSM5499957 c.871G>A p.V291I Substitution - Missense 21:36409417-36409417 + TCGA-B5-A0JV-01 COSM1030539 c.1148C>A p.P383H Substitution - Missense 21:36412970-36412970 + sysucc-1370T COSM5469396 c.1062C>T p.Y354Y Substitution - coding silent 10:28089732-28089732 - TCGA-CG-5721-01 COSM917497 c.1204+1G>A p.? Unknown 10:28069771-28069771 - RK159_C01 COSM1627461 c.851G>A p.R284K Substitution - Missense 10:28120230-28120230 - 2492720 COSM3437069 c.1449G>A p.V483V Substitution - coding silent 10:28056582-28056582 - TCGA-D5-6540-01 COSM1414004 c.1630C>T p.R544W Substitution - Missense 21:36416316-36416316 + TCGA-EB-A44O-01 COSM3437076 c.1063G>A p.E355K Substitution - Missense 10:28089731-28089731 - TCGA-D3-A2JH-06 COSM3437096 c.385G>A p.D129N Substitution - Missense 10:28131622-28131622 - TCGA-13-0760-01 COSM74133 c.112G>T p.D38Y Substitution - Missense 21:36386248-36386248 + 40M COSM1239466 c.358G>A p.D120N Substitution - Missense 10:28131649-28131649 - TCGA-A6-6781-01 COSM1414001 c.191G>A p.R64H Substitution - Missense 21:36387662-36387662 + TCGA-CG-5723-01 COSM2844654 c.1592C>T p.T531M Substitution - Missense 21:36416278-36416278 + 8069453 COSM3769099 c.1223G>A p.R408K Substitution - Missense 10:28059725-28059725 - ZZUFHECRKL-G060T COSM1702217 c.973C>T p.R325C Substitution - Missense 10:28089821-28089821 - YUGOE COSM1702217 c.973C>T p.R325C Substitution - Missense 10:28089821-28089821 - TCGA-B5-A11E-01 COSM106976 c.874C>T p.R292C Substitution - Missense 21:36409420-36409420 + 91603 COSM329249 c.302C>T p.P101L Substitution - Missense 21:36391593-36391593 + SB_07 COSM5753214 c.520G>C p.D174H Substitution - Missense 10:28125019-28125019 - SA219 COSM212438 c.1693G>C p.E565Q Substitution - Missense 10:28054103-28054103 - TCGA-EE-A29L-06 COSM1723512 c.1376C>T p.P459L Substitution - Missense 21:36413198-36413198 + TCGA-FW-A3R5-06 COSM2134770 c.1085G>A p.R362Q Substitution - Missense 10:28089709-28089709 - TCGA-FD-A3B7-01 COSM1307773 c.786A>C p.V262V Substitution - coding silent 21:36408789-36408789 + TCGA-18-3409-01 COSM725200 c.1618C>T p.P540S Substitution - Missense 21:36416304-36416304 + YUDEDE COSM1702220 c.118G>A p.D40N Substitution - Missense 10:28202191-28202191 - BD123T COSM5521131 c.1629G>A p.K543K Substitution - coding silent 21:36416315-36416315 + H522 COSM1197034 c.17C>T p.T6M Substitution - Missense 10:28238588-28238588 - STC263 COSM427444 c.1038C>T p.Y346Y Substitution - coding silent 10:28089756-28089756 - TCGA-DH-A66B-01 COSM3972765 c.722G>C p.S241T Substitution - Missense 21:36402816-36402816 + TCGA-GF-A2C7-01 COSM3437093 c.400G>A p.E134K Substitution - Missense 10:28131607-28131607 - CSCC-56-T COSM4468808 c.1564C>T p.P522S Substitution - Missense 21:36415365-36415365 + PD6744a COSM1637483 c.39G>T p.K13N Substitution - Missense 21:36386175-36386175 + LUAD-5V8LT COSM401032 c.1204C>A p.H402N Substitution - Missense 10:28069772-28069772 - PD4000a COSM159971 c.1255A>C p.T419P Substitution - Missense 21:36413077-36413077 + 19M COSM5578988 c.201C>T p.P67P Substitution - coding silent 10:28150015-28150015 - TCGA-GN-A269-01 COSM3437089 c.550G>A p.E184K Substitution - Missense 10:28124096-28124096 - TCGA-FW-A3R5-06 COSM3867096 c.887G>A p.R296K Substitution - Missense 10:28120194-28120194 - 8031085 COSM3382830 c.1191C>T p.G397G Substitution - coding silent 10:28069785-28069785 - Pat_06_A COSM5836749 c.1376delA p.N459fs*13 Deletion - Frameshift 10:28058526-28058526 - Pat_14_A COSM5836753 c.562_563insGAAG p.V188fs*10 Insertion - Frameshift 10:28124083-28124084 - 2521243 COSM5886679 c.1081C>T p.R361W Substitution - Missense 10:28089713-28089713 - TCGA-B5-A11J-01 COSM1030540 c.1184C>A p.P395H Substitution - Missense 21:36413006-36413006 + TCGA-FW-A3R5-06 COSM3912068 c.1616C>T p.P539L Substitution - Missense 21:36416302-36416302 + Pat_60_B COSM5858595 c.736G>A p.G246R Substitution - Missense 21:36402830-36402830 + TCGA-EE-A29D-06 COSM3437098 c.97G>A p.E33K Substitution - Missense 10:28202212-28202212 - TCGA-ER-A19F-06 COSM3437084 c.751G>A p.E251K Substitution - Missense 10:28120330-28120330 - TCGA-EK-A3GK-01 COSM4854314 c.1170C>T p.I390I Substitution - coding silent 10:28069806-28069806 - BN24 COSM1603377 c.835G>T p.A279S Substitution - Missense 10:28120246-28120246 - TCGA-A2-A0T5-01 COSM159971 c.1255A>C p.T419P Substitution - Missense 21:36413077-36413077 + TCGA-BR-8369-01 COSM1702216 c.1357C>T p.R453W Substitution - Missense 10:28058545-28058545 - 49M COSM5591891 c.244G>A p.E82K Substitution - Missense 10:28147554-28147554 - T3225 COSM1713971 c.1256C>T p.T419I Substitution - Missense 21:36413078-36413078 + Pat_37_B COSM5836755 c.220G>A p.A74T Substitution - Missense 10:28149996-28149996 - YUNEKI COSM5370544 c.569G>A p.G190E Substitution - Missense 10:28124077-28124077 - CHC892T COSM4794543 c.40G>A p.E14K Substitution - Missense 21:36386176-36386176 + TCGA-DU-A5TP-01 COSM3967030 c.974G>A p.R325H Substitution - Missense 10:28089820-28089820 - TCGA-AG-A036-01 COSM290780 c.396G>A p.V132V Substitution - coding silent 21:36394565-36394565 + 587284 COSM1215441 c.780T>G p.D260E Substitution - Missense 10:28120301-28120301 - ME009T COSM224075 c.652G>A p.A218T Substitution - Missense 21:36399594-36399594 + TCGA-EE-A29C-06 COSM3437071 c.1313G>A p.G438E Substitution - Missense 10:28058589-28058589 - YUMOOK COSM1702216 c.1357C>T p.R453W Substitution - Missense 10:28058545-28058545 - TCGA-HT-8563-01 COSM3967031 c.462G>A p.K154K Substitution - coding silent 10:28125077-28125077 - ESO-049 COSM1257907 c.576A>G p.P192P Substitution - coding silent 10:28124070-28124070 - MO_1012 COSM5547507 c.1383delG p.P463fs*24 Deletion - Frameshift 21:36413205-36413205 + TCGA-ER-A19N-06 COSM3437095 c.397G>A p.E133K Substitution - Missense 10:28131610-28131610 - TCGA-D9-A6EC-06 COSM3437076 c.1063G>A p.E355K Substitution - Missense 10:28089731-28089731 - 166 COSM3722570 c.567C>T p.N189N Substitution - coding silent 10:28124079-28124079 - 2492722 COSM3437069 c.1449G>A p.V483V Substitution - coding silent 10:28056582-28056582 - TCGA-BC-A10T-01 COSM4922938 c.411A>G p.V137V Substitution - coding silent 10:28131596-28131596 - TCGA-CZ-4859-01 COSM478564 c.1463C>G p.T488R Substitution - Missense 21:36413285-36413285 + YUZINO COSM1702218 c.448G>A p.G150R Substitution - Missense 10:28125091-28125091 - ESO-859 COSM1239466 c.358G>A p.D120N Substitution - Missense 10:28131649-28131649 - TCGA-EE-A182-06 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - TCGA-IH-A3EA-01 COSM3437069 c.1449G>A p.V483V Substitution - coding silent 10:28056582-28056582 - pfg011T COSM1638543 c.1478G>A p.R493H Substitution - Missense 10:28056553-28056553 - CHEWS011 COSM4582068 c.695G>A p.S232N Substitution - Missense 21:36402789-36402789 + LP6005690-DNA_A02 COSM236161 c.187C>A p.Q63K Substitution - Missense 10:28150029-28150029 - 49M COSM5590193 c.1352C>T p.S451F Substitution - Missense 21:36413174-36413174 + TCGA-EB-A41A-01 COSM3437099 c.56C>T p.A19V Substitution - Missense 10:28202253-28202253 - TCGA-D1-A103-01 COSM917505 c.359A>G p.D120G Substitution - Missense 10:28131648-28131648 - TCGA-JX-A3Q0-01 COSM4824498 c.905G>A p.R302Q Substitution - Missense 10:28119698-28119698 - TCGA-FS-A4F9-06 COSM3437088 c.598G>A p.E200K Substitution - Missense 10:28124048-28124048 - TCGA-ER-A193-06 COSM3550543 c.1079T>G p.F360C Substitution - Missense 21:36412901-36412901 + TCGA-DA-A1I1-06 COSM3437077 c.1039G>A p.D347N Substitution - Missense 10:28089755-28089755 - TCGA-GF-A6C9-06 COSM2134775 c.789G>A p.Q263Q Substitution - coding silent 10:28120292-28120292 - STC246 COSM5057579 c.754C>T p.P252S Substitution - Missense 21:36402848-36402848 + CHC155T COSM3668523 c.827G>A p.R276K Substitution - Missense 21:36408830-36408830 + TCGA-D3-A1QA-06 COSM1239466 c.358G>A p.D120N Substitution - Missense 10:28131649-28131649 - YUKLAB COSM1713971 c.1256C>T p.T419I Substitution - Missense 21:36413078-36413078 + PD6746a COSM1637549 c.73A>G p.T25A Substitution - Missense 21:36386209-36386209 + HCC082T COSM5816290 c.420C>A p.I140I Substitution - coding silent 10:28131587-28131587 - TCGA-B6-A0I5-01 COSM427445 c.298T>C p.S100P Substitution - Missense 10:28147500-28147500 - YUDUTY COSM1713970 c.629C>T p.S210L Substitution - Missense 21:36399571-36399571 + TCGA-EW-A1P4-01 COSM1474578 c.980G>C p.S327T Substitution - Missense 10:28089814-28089814 - TCGA-D1-A103-01 COSM1030538 c.922G>A p.V308M Substitution - Missense 21:36411465-36411465 + TCGA-FS-A1ZB-06 COSM3437090 c.466G>A p.D156N Substitution - Missense 10:28125073-28125073 - 2492722 COSM5724389 c.248C>T p.S83L Substitution - Missense 21:36387719-36387719 + TCGA-D9-A4Z3-01 COSM3437068 c.1482G>A p.L494L Substitution - coding silent 10:28056549-28056549 - CN-AML-NR-08-Dx COSM146915 c.1110C>T p.L370L Substitution - coding silent 10:28089684-28089684 - TCGA-37-4141-01 COSM725202 c.270C>A p.I90I Substitution - coding silent 21:36391561-36391561 + TCGA-EE-A2MS-06 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - 2521243 COSM5887128 c.920-5C>T p.? Unknown 21:36411458-36411458 + Pat_46_B COSM5836751 c.938C>T p.S313F Substitution - Missense 10:28119665-28119665 - 548 COSM5612978 c.824C>T p.A275V Substitution - Missense 10:28120257-28120257 - CHC155T COSM3668523 c.827G>A p.R276K Substitution - Missense 21:36408830-36408830 + 2492721 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - TCGA-AP-A059-01 COSM917500 c.853G>A p.A285T Substitution - Missense 10:28120228-28120228 - TCGA-EE-A2MR-06 COSM3437091 c.434A>T p.N145I Substitution - Missense 10:28131573-28131573 - TCGA-06-0213-01 COSM917503 c.422G>A p.R141H Substitution - Missense 10:28131585-28131585 - 2293773 COSM917503 c.422G>A p.R141H Substitution - Missense 10:28131585-28131585 - 3_PRE-TREATMENT COSM1723610 c.412A>C p.K138Q Substitution - Missense 10:28131595-28131595 - C91 COSM4444307 c.488T>C p.I163T Substitution - Missense 10:28125051-28125051 - TCGA-AP-A051-01 COSM917501 c.544G>T p.G182C Substitution - Missense 10:28124102-28124102 - HT115 COSM2844639 c.688G>A p.D230N Substitution - Missense 21:36402782-36402782 + TCGA-06-0213 COSM917503 c.422G>A p.R141H Substitution - Missense 10:28131585-28131585 - TCGA-BR-7703-01 COSM4013622 c.881A>T p.Q294L Substitution - Missense 10:28120200-28120200 - SC_9017 COSM3722570 c.567C>T p.N189N Substitution - coding silent 10:28124079-28124079 - SC_9081 COSM3382830 c.1191C>T p.G397G Substitution - coding silent 10:28069785-28069785 - B59-Tumor COSM1751627 c.1452C>T p.V484V Substitution - coding silent 21:36413274-36413274 + TCGA-GN-A268-06 COSM3437092 c.421C>T p.R141C Substitution - Missense 10:28131586-28131586 - ATL075 COSM5703556 c.904C>G p.R302G Substitution - Missense 10:28119699-28119699 - 2492722 COSM5724009 c.1306G>A p.E436K Substitution - Missense 10:28058596-28058596 - TCGA-02-2483 COSM2149121 c.756T>C p.A252A Substitution - coding silent 10:28120325-28120325 - TCGA-ER-A198-06 COSM3550544 c.1152G>A p.L384L Substitution - coding silent 21:36412974-36412974 + TCGA-85-6561-01 COSM725201 c.720G>T p.L240L Substitution - coding silent 21:36402814-36402814 + TCGA-D9-A6EC-06 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - TCGA-D5-6529-01 COSM1414003 c.1344C>T p.D448D Substitution - coding silent 21:36413166-36413166 + BD115T COSM5500702 c.44A>G p.Y15C Substitution - Missense 10:28202265-28202265 - TCGA-27-2521-01 COSM3397085 c.1084C>T p.R362* Substitution - Nonsense 10:28089710-28089710 - LAU63 COSM234006 c.616-7T>C p.? Unknown 10:28120675-28120675 - T3182 COSM1560814 c.357C>T p.Y119Y Substitution - coding silent 10:28131650-28131650 - 2492720 COSM5724009 c.1306G>A p.E436K Substitution - Missense 10:28058596-28058596 - PT45 COSM2134780 c.691-4C>T p.? Unknown 10:28120394-28120394 - KM12 COSM1414001 c.191G>A p.R64H Substitution - Missense 21:36387662-36387662 + 6115219 COSM917503 c.422G>A p.R141H Substitution - Missense 10:28131585-28131585 - TCGA-EE-A29S-06 COSM3437094 c.399G>A p.E133E Substitution - coding silent 10:28131608-28131608 - TCGA-D3-A2J7-06 COSM3437080 c.945G>A p.R315R Substitution - coding silent 10:28119658-28119658 - AOCS-063-1-3 COSM4137235 c.1615C>T p.P539S Substitution - Missense 21:36416301-36416301 + TCGA-BR-4256-01 COSM4013623 c.339T>C p.T113T Substitution - coding silent 10:28131668-28131668 - PT40 COSM1702217 c.973C>T p.R325C Substitution - Missense 10:28089821-28089821 - TCGA-CC-A123-01 COSM4915345 c.1289C>A p.P430H Substitution - Missense 21:36413111-36413111 + TCGA-EE-A2GC-06 COSM3437087 c.682G>A p.E228K Substitution - Missense 10:28120602-28120602 - SNUH_G16_S1 COSM3997934 c.1110C>G p.L370L Substitution - coding silent 10:28089684-28089684 - sysucc-1972T COSM5480310 c.625C>T p.Q209* Substitution - Nonsense 10:28120659-28120659 - H1672 COSM310070 c.1462A>G p.T488A Substitution - Missense 21:36413284-36413284 + B59 COSM1751627 c.1452C>T p.V484V Substitution - coding silent 21:36413274-36413274 + OV207 COSM252434 c.282G>T p.K94N Substitution - Missense 21:36391573-36391573 + TCGA-DA-A1IC-06 COSM3437076 c.1063G>A p.E355K Substitution - Missense 10:28089731-28089731 - Au3 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - 40M COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - SWE-4C COSM5521490 c.862A>G p.T288A Substitution - Missense 21:36409408-36409408 + PCSI_0020_Pa_X COSM304709 c.437C>T p.S146F Substitution - Missense 21:36394606-36394606 + TCGA-FW-A3R5-06 COSM3867095 c.1205-1G>A p.? Unknown 10:28059744-28059744 - HCT116 COSM4631947 c.198G>A p.V66V Substitution - coding silent 10:28150018-28150018 - TCGA-AP-A051-01 COSM1030535 c.127-1G>T p.? Unknown 21:36387597-36387597 + C086 COSM1239466 c.358G>A p.D120N Substitution - Missense 10:28131649-28131649 - TCGA-ER-A19K-01 COSM3437074 c.1096G>A p.E366K Substitution - Missense 10:28089698-28089698 - PD4978a COSM4806711 c.313G>A p.A105T Substitution - Missense 21:36391604-36391604 + HCC131T COSM5824600 c.1350C>T p.D450D Substitution - coding silent 10:28058552-28058552 - CRC-1 COSM304709 c.437C>T p.S146F Substitution - Missense 21:36394606-36394606 + LUAD-QCHM7 COSM377112 c.1663C>G p.L555V Substitution - Missense 10:28054133-28054133 - TCGA-DA-A1IC-06 COSM917502 c.483G>A p.A161A Substitution - coding silent 10:28125056-28125056 - YUBER COSM1702215 c.1486G>A p.E496K Substitution - Missense 10:28056545-28056545 - 587376 COSM1200936 c.673T>G p.Y225D Substitution - Missense 21:36402767-36402767 + 46M COSM5587485 c.1244C>T p.P415L Substitution - Missense 21:36413066-36413066 + TCGA-B5-A0JY-01 COSM917504 c.414A>C p.K138N Substitution - Missense 10:28131593-28131593 - TCGA-AC-A62Y-01 COSM3807003 c.580G>T p.E194* Substitution - Nonsense 10:28124066-28124066 - TCGA-FW-A3R5-06 COSM2134748 c.1660G>A p.E554K Substitution - Missense 10:28054136-28054136 - TCGA-G2-A3IE-01 COSM1297201 c.1287A>G p.V429V Substitution - coding silent 10:28059661-28059661 - 2492720 COSM5724389 c.248C>T p.S83L Substitution - Missense 21:36387719-36387719 + TCGA-DD-A4NV-01 COSM4916310 c.1017A>G p.E339E Substitution - coding silent 10:28089777-28089777 - HCC153T COSM5823227 c.815G>C p.W272S Substitution - Missense 10:28120266-28120266 - HCT116 COSM2134785 c.228C>T p.A76A Substitution - coding silent 10:28149988-28149988 - TCGA-D3-A2JH-06 COSM3437078 c.1007C>T p.S336F Substitution - Missense 10:28089787-28089787 - T2284 COSM4671916 c.708C>T p.F236F Substitution - coding silent 21:36402802-36402802 + YURAY COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - 3_RESISTANT COSM1723512 c.1376C>T p.P459L Substitution - Missense 21:36413198-36413198 + 2492723 COSM5724389 c.248C>T p.S83L Substitution - Missense 21:36387719-36387719 + TCGA-D3-A2J8-06 COSM3437072 c.1299-1G>A p.? Unknown 10:28058604-28058604 - RK077_C01 COSM3740289 c.1562C>A p.T521N Substitution - Missense 21:36415363-36415363 + TCGA-D1-A16Y-01 COSM1030537 c.489G>T p.K163N Substitution - Missense 21:36397422-36397422 + 2492721 COSM3437069 c.1449G>A p.V483V Substitution - coding silent 10:28056582-28056582 - HONE1 COSM4996055 c.1280C>G p.P427R Substitution - Missense 21:36413102-36413102 + TCGA-D9-A149-06 COSM1239466 c.358G>A p.D120N Substitution - Missense 10:28131649-28131649 - CN-AML-08-T COSM146915 c.1110C>T p.L370L Substitution - coding silent 10:28089684-28089684 - YUZINO COSM1702214 c.1612C>T p.L538F Substitution - Missense 10:28054184-28054184 - TCGA-02-2483 COSM2149126 c.757G>T p.G253W Substitution - Missense 10:28120324-28120324 - TCGA-AP-A0LM-01 COSM1030536 c.190C>T p.R64C Substitution - Missense 21:36387661-36387661 + 2492721 COSM5724009 c.1306G>A p.E436K Substitution - Missense 10:28058596-28058596 - EGC15 COSM5057580 c.1048A>G p.S350G Substitution - Missense 21:36411591-36411591 + 2492720 COSM2134766 c.1157G>A p.R386Q Substitution - Missense 10:28069819-28069819 - 587234 COSM1200935 c.571T>G p.C191G Substitution - Missense 21:36397504-36397504 + 2492723 COSM3437069 c.1449G>A p.V483V Substitution - coding silent 10:28056582-28056582 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.75238 21q22.13 601245 2410401|CGAP|BC021218|G/T|coding|Gly36Cys|175|Candidate Hs.499159 10p12.1 610973

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.T419P c.1255A>C 21 37785375 BRCA A C Synonymous p.V262V c.786A>C 21 37781087 BLCA A G IntronicSNV . c.260-1742A>G 21 37762107 CLL A G Missense p.Q528R c.1583A>G 21 37787682 LGG A G Missense p.T332A c.994A>G 21 37783835 RCCC A G Synonymous p.V197V c.591A>G 21 37771831 BRCA A T Missense p.I344L c.1030A>T 21 37783871 HNSC C A Missense p.P383H c.1148C>A 21 37785268 UCEC C A Missense p.P395H c.1184C>A 21 37785304 UCEC C A Synonymous p.I90I c.270C>A 21 37763859 LUSC CC TT Missense p.R238C c.711_712delinsTT 21 37775103 CM CG AT Missense p.P295H c.884_885delinsAT 21 37781728 CM C G Missense p.T488R c.1463C>G 21 37785583 RCCC C T Missense p.P459L c.1376C>T 21 37785496 CM C T Missense p.R126W c.376C>T 21 37763965 STAD C T Missense p.S326F c.977C>T 21 37783818 CM C T Synonymous p.F242F c.726C>T 21 37775118 LUAD C T Synonymous p.I154I c.462C>T 21 37766929 BLCA C T Synonymous p.P427P c.1281C>T 21 37785401 CM C T Synonymous p.S355S c.1065C>T 21 37785185 CM G A Missense p.A218T c.652G>A 21 37771892 CM G A Missense p.G552E c.1655G>A 21 37788639 HNSC G A Synonymous p.L384L c.1152G>A 21 37785272 CM G A Synonymous p.V132V c.396G>A 21 37766863 COREAD G T Missense p.D38Y c.112G>T 21 37758546 OV G T Missense p.K163N c.489G>T 21 37769720 UCEC G T Missense p.K234N c.702G>T 21 37775094 CM G T Missense p.R196L c.587G>T 21 37771827 CM G T Missense p.R393I c.1178G>T 21 37785298 HNSC G T Synonymous p.L240L c.720G>T 21 37775112 LUSC T G Missense p.F360C c.1079T>G 21 37785199 CM T - IntronicDeletion . c.482-5delT 21 37769701 STAD AC - IntronicDeletion . c.156+2272_156+2273delGT 10 28488809 CM A G IntronicSNV . c.156+21884T>C 10 28469198 CLL A G Missense p.S100P c.298T>C 10 28436429 BRCA A G Synonymous p.L326L c.978T>C 10 28378745 CM A G Synonymous p.T113T c.339T>C 10 28420597 STAD A T IntronicSNV . c.38-15360T>A 10 28506560 CLL A T Missense p.W568R c.1702T>A 10 28343023 COREAD A T Synonymous p.G414G c.1242T>A 10 28348635 LUSC CA AG Missense p.G253W c.756_757delinsCT 10 28409253 GBM C A Missense p.S448I c.1343G>T 10 28347488 CM C A Missense p.V122L c.364G>T 10 28420572 LUSC C A Synonymous p.P359P c.1077G>T 10 28378646 LUAD C G 3-UTRSNV . c.1728+451G>C 10 28342546 HC C G Missense p.E565Q c.1693G>C 10 28343032 BRCA C G Missense p.R296S c.888G>C 10 28408644 OV C G Missense p.S327T c.980G>C 10 28378743 BRCA C T IntronicSNV . c.37+17002G>A 10 28510495 CLL C T Missense p.D112N c.334G>A 10 28420602 CM C T Missense p.D120N c.358G>A 10 28420578 CM C T Missense p.D120N c.358G>A 10 28420578 ESCA C T Missense p.D129N c.385G>A 10 28420551 CM C T Missense p.D156N c.466G>A 10 28414002 CM C T Missense p.D347N c.1039G>A 10 28378684 CM C T Missense p.D413N c.1237G>A 10 28348640 CM C T Missense p.E133K c.397G>A 10 28420539 CM C T Missense p.E134K c.400G>A 10 28420536 CM C T Missense p.E184K c.550G>A 10 28413025 CM C T Missense p.E228K c.682G>A 10 28409531 CM C T Missense p.E251K c.751G>A 10 28409259 CM C T Missense p.E355K c.1063G>A 10 28378660 CM C T Missense p.E355K c.1063G>A 10 28378660 STAD C T Missense p.E366K c.1096G>A 10 28378627 CM C T Missense p.E383K c.1147G>A 10 28358758 CM C T Missense p.E532K c.1594G>A 10 28343131 CM C T Missense p.G438E c.1313G>A 10 28347518 CM C T Missense p.G511S c.1531G>A 10 28345429 CM C T Missense p.R141H c.422G>A 10 28420514 GBM C T Missense p.R361Q c.1082G>A 10 28378641 UCEC C T Missense p.R386Q c.1157G>A 10 28358748 CM C T Missense p.R493H c.1478G>A 10 28345482 STAD C T Missense p.V137I c.409G>A 10 28420527 CM C T SpliceAcceptorSNV . c.1299-1G>A 10 28347533 CM C T SpliceDonorSNV . c.1407+1G>A 10 28347423 UCEC C T Synonymous p.A161A c.483G>A 10 28413985 CM C T Synonymous p.E133E c.399G>A 10 28420537 CM C T Synonymous p.K487K c.1461G>A 10 28345499 CM C T Synonymous p.Q203Q c.609G>A 10 28412966 CM C T Synonymous p.R315R c.945G>A 10 28408587 CM C T Synonymous p.T6T c.18G>A 10 28527516 COREAD C T Synonymous p.V471V c.1413G>A 10 28345547 LUSC C T Synonymous p.V483V c.1449G>A 10 28345511 CM CTTC - IntronicDeletion . c.1407+742_1407+745delAAGA 10 28346679 HC G A 3-UTRSNV . c.1728+1015C>T 10 28341982 HC G A 3-UTRSNV . c.1728+17C>T 10 28342980 CM G A 5-UTRSNV . c.1-59C>T 10 28527592 CM G A IntronicSNV . c.1298+26C>T 10 28348553 CM G A IntronicSNV . c.952+2025C>T 10 28406555 PIA G A Missense p.P248S c.742C>T 10 28409268 CM G A Missense p.P359S c.1075C>T 10 28378648 CM G A Missense p.R141C c.421C>T 10 28420515 CM G A Missense p.S313F c.938C>T 10 28408594 CM G A Missense p.S336F c.1007C>T 10 28378716 CM G A Missense p.T403I c.1208C>T 10 28348669 LUSC G A Nonsense p.Q263* c.787C>T 10 28409223 CM G A Nonsense p.R362* c.1084C>T 10 28378639 GBM G A Synonymous p.D350D c.1050C>T 10 28378673 STAD G A Synonymous p.F293F c.879C>T 10 28409131 CM G A Synonymous p.N189N c.567C>T 10 28413008 HNSC G A Synonymous p.P283P c.849C>T 10 28409161 CM G A Synonymous p.Y346Y c.1038C>T 10 28378685 BRCA G C IntronicSNV . c.157-6297C>G 10 28445285 CLL G C IntronicSNV . c.38-3098C>G 10 28494298 PIA G C Missense p.I233M c.699C>G 10 28409311 BLCA G T Missense p.P489Q c.1466C>A 10 28345494 LUSC T A Missense p.K329N c.987A>T 10 28378736 CM T A Nonsense p.R407* c.1219A>T 10 28348658 STAD T C Missense p.K433E c.1297A>G 10 28348580 LUSC T C Missense p.S90G c.268A>G 10 28436459 SCLC T C Synonymous p.P192P c.576A>G 10 28412999 ESCA T C Synonymous p.T497T c.1491A>G 10 28345469 GBM T C Synonymous p.V429V c.1287A>G 10 28348590 BLCA T G Missense p.K258Q c.772A>C 10 28409238 CM