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 23 21674383 21674383 + Silent SNP C C T TCGA-ZF-A9RN-01A-11D-A42E-08 TCGA-ZF-A9RN-10A-01D-A42H-08 g.chrX:21674383C>T c.1524G>A c.(1522-1524)aaG>aaA p.K508K BLCA 23 21674415 21674415 + Missense_Mutation SNP C C A TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chrX:21674415C>A c.1492G>T c.(1492-1494)Gtc>Ttc p.V498F BLCA 23 21674920 21674922 + In_Frame_Del DEL CTC CTC - TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chrX:21674920_21674922delCTC c.985_987delGAG c.(985-987)gagdel p.E329del BLCA 23 21675005 21675005 + Missense_Mutation SNP G G A TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chrX:21675005G>A c.902C>T c.(901-903)cCg>cTg p.P301L BLCA 23 21675187 21675187 + Silent SNP A A G TCGA-E7-A3Y1-01A-11D-A22Z-08 TCGA-E7-A3Y1-10A-01D-A22Z-08 g.chrX:21675187A>G c.720T>C c.(718-720)tcT>tcC p.S240S BLCA 23 21675859 21675859 + Silent SNP G G T TCGA-E7-A677-01A-11D-A30E-08 TCGA-E7-A677-10A-01D-A30H-08 g.chrX:21675859G>T c.48C>A c.(46-48)ctC>ctA p.L16L BRCA 23 21674415 21674415 + Missense_Mutation SNP C C T TCGA-EW-A1OY-01A-11D-A142-09 TCGA-EW-A1OY-10A-01W-A187-09 g.chrX:21674415C>T c.1492G>A c.(1492-1494)Gtc>Atc p.V498I BRCA 23 21674481 21674481 + Frame_Shift_Del DEL C C - TCGA-AN-A0FN-01A-11W-A050-09 TCGA-AN-A0FN-10A-01W-A055-09 g.chrX:21674481delC c.1426delG c.(1426-1428)gtgfs p.V476fs BRCA 23 21675045 21675046 + Frame_Shift_Ins INS - - C TCGA-AO-A03R-01A-21W-A050-09 TCGA-AO-A03R-10A-01W-A055-09 g.chrX:21675045_21675046insC c.861_862insG c.(859-864)gggcgcfs p.R288fs BRCA 23 21675045 21675046 + Frame_Shift_Ins INS - - C TCGA-BH-A0DZ-01A-11W-A019-09 TCGA-BH-A0DZ-10A-01W-A021-09 g.chrX:21675045_21675046insC c.861_862insG c.(859-864)gggcgcfs p.R288fs BRCA 23 21675572 21675572 + Missense_Mutation SNP G G T TCGA-A8-A07I-01A-11W-A019-09 TCGA-A8-A07I-10A-01W-A021-09 g.chrX:21675572G>T c.335C>A c.(334-336)aCt>aAt p.T112N CESC 23 21675600 21675600 + Silent SNP G G A TCGA-DS-A0VM-01A-11D-A10S-08 TCGA-DS-A0VM-10A-01D-A10S-08 g.chrX:21675600G>A c.307C>T c.(307-309)Ctg>Ttg p.L103L COAD 23 21674156 21674156 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:21674156G>A c.1751C>T c.(1750-1752)tCg>tTg p.S584L COAD 23 21674234 21674234 + Missense_Mutation SNP G G T TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chrX:21674234G>T c.1673C>A c.(1672-1674)cCc>cAc p.P558H COAD 23 21674283 21674283 + Missense_Mutation SNP C C T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chrX:21674283C>T c.1624G>A c.(1624-1626)Gag>Aag p.E542K COAD 23 21674284 21674284 + Silent SNP G G A TCGA-AA-3502-01A-01D-1408-10 TCGA-AA-3502-11A-01D-1408-10 g.chrX:21674284G>A c.1623C>T c.(1621-1623)atC>atT p.I541I COAD 23 21674365 21674365 + Silent SNP G G A TCGA-AA-3527-01A-01W-0831-10 TCGA-AA-3527-10A-01W-0831-10 g.chrX:21674365G>A c.1542C>T c.(1540-1542)acC>acT p.T514T COAD 23 21674707 21674707 + Silent SNP C C T TCGA-DM-A0XF-01A-11D-A152-10 TCGA-DM-A0XF-10A-01D-A152-10 g.chrX:21674707C>T c.1200G>A c.(1198-1200)ccG>ccA p.P400P COAD 23 21674812 21674812 + Silent SNP G G T TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chrX:21674812G>T c.1095C>A c.(1093-1095)ggC>ggA p.G365G COAD 23 21674920 21674922 + In_Frame_Del DEL CTC CTC - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chrX:21674920_21674922delCTC c.985_987delGAG c.(985-987)gagdel p.E329del COAD 23 21675046 21675046 + Frame_Shift_Del DEL C C - TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:21675046delC c.861delG c.(859-861)gggfs p.G287fs COAD 23 21675046 21675046 + Frame_Shift_Del DEL C C - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chrX:21675046delC c.861delG c.(859-861)gggfs p.G287fs COAD 23 21675046 21675046 + Frame_Shift_Del DEL C C - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:21675046delC c.861delG c.(859-861)gggfs p.G287fs COAD 23 21675046 21675046 + Frame_Shift_Del DEL C C - TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chrX:21675046delC c.861delG c.(859-861)gggfs p.G287fs COAD 23 21675080 21675080 + Missense_Mutation SNP C C T TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chrX:21675080C>T c.827G>A c.(826-828)cGg>cAg p.R276Q COAD 23 21675338 21675338 + Missense_Mutation SNP C C T TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chrX:21675338C>T c.569G>A c.(568-570)cGg>cAg p.R190Q COAD 23 21675346 21675346 + Silent SNP G G A TCGA-AA-3818-01A-01W-0900-09 TCGA-AA-3818-10A-01W-0900-09 g.chrX:21675346G>A c.561C>T c.(559-561)gaC>gaT p.D187D COAD 23 21675634 21675634 + Nonsense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:21675634C>T c.273G>A c.(271-273)tgG>tgA p.W91* COAD 23 21675704 21675704 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chrX:21675704C>T c.203G>A c.(202-204)cGc>cAc p.R68H COAD 23 21675868 21675868 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:21675868G>A c.39C>T c.(37-39)ggC>ggT p.G13G COADREAD 23 21674156 21674156 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:21674156G>A c.1751C>T c.(1750-1752)tCg>tTg p.S584L COADREAD 23 21674234 21674234 + Missense_Mutation SNP G G T TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chrX:21674234G>T c.1673C>A c.(1672-1674)cCc>cAc p.P558H COADREAD 23 21674283 21674283 + Missense_Mutation SNP C C T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chrX:21674283C>T c.1624G>A c.(1624-1626)Gag>Aag p.E542K COADREAD 23 21674284 21674284 + Silent SNP G G A TCGA-AA-3502-01A-01D-1408-10 TCGA-AA-3502-11A-01D-1408-10 g.chrX:21674284G>A c.1623C>T c.(1621-1623)atC>atT p.I541I COADREAD 23 21674365 21674365 + Silent SNP G G A TCGA-AA-3527-01A-01W-0831-10 TCGA-AA-3527-10A-01W-0831-10 g.chrX:21674365G>A c.1542C>T c.(1540-1542)acC>acT p.T514T COADREAD 23 21674619 21674619 + Missense_Mutation SNP C C T TCGA-CL-5917-01A-11D-1657-10 TCGA-CL-5917-10A-01D-1657-10 g.chrX:21674619C>T c.1288G>A c.(1288-1290)Gtc>Atc p.V430I COADREAD 23 21674707 21674707 + Silent SNP C C T TCGA-DM-A0XF-01A-11D-A152-10 TCGA-DM-A0XF-10A-01D-A152-10 g.chrX:21674707C>T c.1200G>A c.(1198-1200)ccG>ccA p.P400P COADREAD 23 21674812 21674812 + Silent SNP G G T TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chrX:21674812G>T c.1095C>A c.(1093-1095)ggC>ggA p.G365G COADREAD 23 21674920 21674922 + In_Frame_Del DEL CTC CTC - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chrX:21674920_21674922delCTC c.985_987delGAG c.(985-987)gagdel p.E329del COADREAD 23 21675045 21675046 + Frame_Shift_Ins INS - - C TCGA-AG-3727-01A-01W-0899-10 TCGA-AG-3727-10A-01W-0901-10 g.chrX:21675045_21675046insC c.861_862insG c.(859-864)gggcgcfs p.R288fs COADREAD 23 21675046 21675046 + Frame_Shift_Del DEL C C - TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:21675046delC c.861delG c.(859-861)gggfs p.G287fs COADREAD 23 21675046 21675046 + Frame_Shift_Del DEL C C - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chrX:21675046delC c.861delG c.(859-861)gggfs p.G287fs COADREAD 23 21675046 21675046 + Frame_Shift_Del DEL C C - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:21675046delC c.861delG c.(859-861)gggfs p.G287fs COADREAD 23 21675046 21675046 + Frame_Shift_Del DEL C C - TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chrX:21675046delC c.861delG c.(859-861)gggfs p.G287fs COADREAD 23 21675080 21675080 + Missense_Mutation SNP C C T TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chrX:21675080C>T c.827G>A c.(826-828)cGg>cAg p.R276Q COADREAD 23 21675338 21675338 + Missense_Mutation SNP C C T TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chrX:21675338C>T c.569G>A c.(568-570)cGg>cAg p.R190Q COADREAD 23 21675346 21675346 + Silent SNP G G A TCGA-AA-3818-01A-01W-0900-09 TCGA-AA-3818-10A-01W-0900-09 g.chrX:21675346G>A c.561C>T c.(559-561)gaC>gaT p.D187D COADREAD 23 21675634 21675634 + Nonsense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:21675634C>T c.273G>A c.(271-273)tgG>tgA p.W91* COADREAD 23 21675704 21675704 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chrX:21675704C>T c.203G>A c.(202-204)cGc>cAc p.R68H COADREAD 23 21675868 21675868 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:21675868G>A c.39C>T c.(37-39)ggC>ggT p.G13G DLBC 23 21675125 21675125 + Missense_Mutation SNP G G A TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chrX:21675125G>A c.782C>T c.(781-783)aCg>aTg p.T261M ESCA 23 21674919 21674920 + In_Frame_Ins INS - - CTC TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chrX:21674919_21674920insCTC c.987_988insGAG c.(985-990)gagtgg>gagGAGtgg p.329_330insE ESCA 23 21674920 21674922 + In_Frame_Del DEL CTC CTC - TCGA-L5-A8NH-01A-11D-A37C-09 TCGA-L5-A8NH-11A-11D-A37F-09 g.chrX:21674920_21674922delCTC c.985_987delGAG c.(985-987)gagdel p.E329del GBM 23 21674007 21674007 + Missense_Mutation SNP C C T TCGA-19-1390-01A-01D-1495-08 TCGA-19-1390-10C-01D-1495-08 g.chrX:21674007C>T c.1900G>A c.(1900-1902)Gag>Aag p.E634K GBM 23 21674666 21674666 + Missense_Mutation SNP G G A TCGA-02-0055-01A-01D-1490-08 TCGA-02-0055-10A-01D-1490-08 g.chrX:21674666G>A c.1241C>T c.(1240-1242)gCg>gTg p.A414V GBM 23 21675201 21675201 + Missense_Mutation SNP C C T TCGA-06-2558-01A-01D-1494-08 TCGA-06-2558-10A-01D-1494-08 g.chrX:21675201C>T c.706G>A c.(706-708)Gtg>Atg p.V236M GBM 23 21675213 21675213 + Missense_Mutation SNP C C G TCGA-76-4935-01A-01D-1486-08 TCGA-76-4935-10A-01D-1486-08 g.chrX:21675213C>G c.694G>C c.(694-696)Gta>Cta p.V232L GBM 23 21675508 21675508 + Silent SNP G G A TCGA-28-6450-01A-11D-1696-08 TCGA-28-6450-10A-01D-1696-08 g.chrX:21675508G>A c.399C>T c.(397-399)ttC>ttT p.F133F GBMLGG 23 21674007 21674007 + Missense_Mutation SNP C C T TCGA-19-1390-01A-01D-1495-08 TCGA-19-1390-10C-01D-1495-08 g.chrX:21674007C>T c.1900G>A c.(1900-1902)Gag>Aag p.E634K GBMLGG 23 21674666 21674666 + Missense_Mutation SNP G G A TCGA-02-0055-01A-01D-1490-08 TCGA-02-0055-10A-01D-1490-08 g.chrX:21674666G>A c.1241C>T c.(1240-1242)gCg>gTg p.A414V GBMLGG 23 21674920 21674922 + In_Frame_Del DEL CTC CTC - TCGA-FG-8181-01A-11D-2253-08 TCGA-FG-8181-10A-01D-2253-08 g.chrX:21674920_21674922delCTC c.985_987delGAG c.(985-987)gagdel p.E329del GBMLGG 23 21675201 21675201 + Missense_Mutation SNP C C T TCGA-06-2558-01A-01D-1494-08 TCGA-06-2558-10A-01D-1494-08 g.chrX:21675201C>T c.706G>A c.(706-708)Gtg>Atg p.V236M GBMLGG 23 21675213 21675213 + Missense_Mutation SNP C C G TCGA-76-4935-01A-01D-1486-08 TCGA-76-4935-10A-01D-1486-08 g.chrX:21675213C>G c.694G>C c.(694-696)Gta>Cta p.V232L GBMLGG 23 21675338 21675338 + Missense_Mutation SNP C C T TCGA-TQ-A7RJ-01A-11D-A33T-08 TCGA-TQ-A7RJ-10A-01D-A33W-08 g.chrX:21675338C>T c.569G>A c.(568-570)cGg>cAg p.R190Q GBMLGG 23 21675508 21675508 + Silent SNP G G A TCGA-28-6450-01A-11D-1696-08 TCGA-28-6450-10A-01D-1696-08 g.chrX:21675508G>A c.399C>T c.(397-399)ttC>ttT p.F133F GBMLGG 23 21675840 21675840 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:21675840G>A c.67C>T c.(67-69)Cgc>Tgc p.R23C HNSC 23 21674052 21674052 + Missense_Mutation SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chrX:21674052C>T c.1855G>A c.(1855-1857)Gca>Aca p.A619T HNSC 23 21674328 21674328 + Missense_Mutation SNP C C A TCGA-QK-A8Z8-01A-11D-A391-08 TCGA-QK-A8Z8-10A-01D-A394-08 g.chrX:21674328C>A c.1579G>T c.(1579-1581)Gct>Tct p.A527S HNSC 23 21674708 21674708 + Missense_Mutation SNP G G T TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chrX:21674708G>T c.1199C>A c.(1198-1200)cCg>cAg p.P400Q HNSC 23 21674749 21674749 + Silent SNP G G A TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chrX:21674749G>A c.1158C>T c.(1156-1158)gaC>gaT p.D386D HNSC 23 21675044 21675044 + Missense_Mutation SNP C C T TCGA-IQ-A61K-01A-11D-A30E-08 TCGA-IQ-A61K-10A-01D-A30H-08 g.chrX:21675044C>T c.863G>A c.(862-864)cGc>cAc p.R288H HNSC 23 21675148 21675148 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chrX:21675148G>A c.759C>T c.(757-759)atC>atT p.I253I HNSC 23 21675186 21675186 + Missense_Mutation SNP C C A TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chrX:21675186C>A c.721G>T c.(721-723)Ggc>Tgc p.G241C HNSC 23 21675204 21675204 + Missense_Mutation SNP G G T TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chrX:21675204G>T c.703C>A c.(703-705)Cgc>Agc p.R235S HNSC 23 21675273 21675273 + Missense_Mutation SNP G G T TCGA-HD-A634-01A-11D-A28R-08 TCGA-HD-A634-10A-01D-A28U-08 g.chrX:21675273G>T c.634C>A c.(634-636)Cgc>Agc p.R212S HNSC 23 21675713 21675713 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chrX:21675713G>A c.194C>T c.(193-195)tCc>tTc p.S65F KICH 23 21675168 21675168 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chrX:21675168G>A c.739C>T c.(739-741)Cgg>Tgg p.R247W KIPAN 23 21674384 21674384 + Frame_Shift_Del DEL T T - TCGA-CJ-4640-01A-02D-1386-10 TCGA-CJ-4640-11A-01D-1251-10 g.chrX:21674384delT c.1523delA c.(1522-1524)aagfs p.K509fs KIPAN 23 21674429 21674429 + Missense_Mutation SNP A A G TCGA-A4-A7UZ-01A-12D-A34Z-10 TCGA-A4-A7UZ-10A-01D-A34Z-10 g.chrX:21674429A>G c.1478T>C c.(1477-1479)cTc>cCc p.L493P KIPAN 23 21674907 21674907 + Missense_Mutation SNP G G T TCGA-CJ-6032-01A-11D-1669-08 TCGA-CJ-6032-11A-01D-1669-08 g.chrX:21674907G>T c.1000C>A c.(1000-1002)Cag>Aag p.Q334K KIPAN 23 21675168 21675168 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chrX:21675168G>A c.739C>T c.(739-741)Cgg>Tgg p.R247W KIRC 23 21674384 21674384 + Frame_Shift_Del DEL T T - TCGA-CJ-4640-01A-02D-1386-10 TCGA-CJ-4640-11A-01D-1251-10 g.chrX:21674384delT c.1523delA c.(1522-1524)aagfs p.K509fs KIRC 23 21674907 21674907 + Missense_Mutation SNP G G T TCGA-CJ-6032-01A-11D-1669-08 TCGA-CJ-6032-11A-01D-1669-08 g.chrX:21674907G>T c.1000C>A c.(1000-1002)Cag>Aag p.Q334K KIRP 23 21674429 21674429 + Missense_Mutation SNP A A G TCGA-A4-A7UZ-01A-12D-A34Z-10 TCGA-A4-A7UZ-10A-01D-A34Z-10 g.chrX:21674429A>G c.1478T>C c.(1477-1479)cTc>cCc p.L493P LGG 23 21674920 21674922 + In_Frame_Del DEL CTC CTC - TCGA-FG-8181-01A-11D-2253-08 TCGA-FG-8181-10A-01D-2253-08 g.chrX:21674920_21674922delCTC c.985_987delGAG c.(985-987)gagdel p.E329del LGG 23 21675338 21675338 + Missense_Mutation SNP C C T TCGA-TQ-A7RJ-01A-11D-A33T-08 TCGA-TQ-A7RJ-10A-01D-A33W-08 g.chrX:21675338C>T c.569G>A c.(568-570)cGg>cAg p.R190Q LGG 23 21675840 21675840 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:21675840G>A c.67C>T c.(67-69)Cgc>Tgc p.R23C LUAD 23 21674057 21674057 + Missense_Mutation SNP C C A TCGA-55-7910-01A-11D-2167-08 TCGA-55-7910-11A-01D-2167-08 g.chrX:21674057C>A c.1850G>T c.(1849-1851)cGg>cTg p.R617L LUAD 23 21674113 21674113 + Silent SNP G G A TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chrX:21674113G>A c.1794C>T c.(1792-1794)gaC>gaT p.D598D LUAD 23 21674179 21674179 + Silent SNP C C G TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chrX:21674179C>G c.1728G>C c.(1726-1728)ctG>ctC p.L576L LUAD 23 21674276 21674276 + Missense_Mutation SNP T T C TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chrX:21674276T>C c.1631A>G c.(1630-1632)tAc>tGc p.Y544C LUAD 23 21674331 21674331 + Missense_Mutation SNP C C A TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chrX:21674331C>A c.1576G>T c.(1576-1578)Ggc>Tgc p.G526C LUAD 23 21674661 21674661 + Missense_Mutation SNP C C T TCGA-97-7547-01A-11D-2036-08 TCGA-97-7547-10A-01D-2036-08 g.chrX:21674661C>T c.1246G>A c.(1246-1248)Gcc>Acc p.A416T LUAD 23 21674670 21674670 + Nonsense_Mutation SNP C C A TCGA-NJ-A55R-01A-11D-A25L-08 TCGA-NJ-A55R-10A-01D-A25L-08 g.chrX:21674670C>A c.1237G>T c.(1237-1239)Gaa>Taa p.E413* LUAD 23 21674705 21674705 + Missense_Mutation SNP C C T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chrX:21674705C>T c.1202G>A c.(1201-1203)cGc>cAc p.R401H LUAD 23 21674752 21674752 + Silent SNP G G T TCGA-86-8281-01A-11D-2284-08 TCGA-86-8281-10A-01D-2284-08 g.chrX:21674752G>T c.1155C>A c.(1153-1155)gcC>gcA p.A385A LUAD 23 21674824 21674824 + Silent SNP C C A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chrX:21674824C>A c.1083G>T c.(1081-1083)gtG>gtT p.V361V LUAD 23 21675066 21675066 + Frame_Shift_Del DEL G G - TCGA-55-8205-01A-11D-2238-08 TCGA-55-8205-10A-01D-2238-08 g.chrX:21675066delG c.841delC c.(841-843)cgcfs p.R281fs LUAD 23 21675117 21675117 + Missense_Mutation SNP G G A TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chrX:21675117G>A c.790C>T c.(790-792)Cgc>Tgc p.R264C LUAD 23 21675157 21675157 + Silent SNP G G T TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chrX:21675157G>T c.750C>A c.(748-750)ggC>ggA p.G250G LUAD 23 21675499 21675499 + Missense_Mutation SNP G G C TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chrX:21675499G>C c.408C>G c.(406-408)aaC>aaG p.N136K LUAD 23 21675702 21675703 + Frame_Shift_Del DEL CG CG - TCGA-86-7711-01A-11D-2063-08 TCGA-86-7711-10A-01D-2063-08 g.chrX:21675702_21675703delCG c.204_205delCG c.(202-207)cgcgtgfs p.V69fs LUAD 23 21675703 21675703 + Silent SNP G G T TCGA-55-A493-01A-11D-A24D-08 TCGA-55-A493-10A-01D-A24F-08 g.chrX:21675703G>T c.204C>A c.(202-204)cgC>cgA p.R68R LUAD 23 21675802 21675802 + Silent SNP G G T TCGA-44-A479-01A-31D-A24D-08 TCGA-44-A479-10A-01D-A24F-08 g.chrX:21675802G>T c.105C>A c.(103-105)acC>acA p.T35T LUAD 23 21675838 21675838 + Silent SNP G G T TCGA-78-7152-01A-11D-2036-08 TCGA-78-7152-10A-01D-2036-08 g.chrX:21675838G>T c.69C>A c.(67-69)cgC>cgA p.R23R LUAD 23 21675867 21675867 + Missense_Mutation SNP C C T TCGA-55-A494-01A-11D-A24P-08 TCGA-55-A494-10A-01D-A24P-08 g.chrX:21675867C>T c.40G>A c.(40-42)Gcg>Acg p.A14T LUSC 23 21674689 21674689 + Silent SNP C C A TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chrX:21674689C>A c.1218G>T c.(1216-1218)acG>acT p.T406T LUSC 23 21675117 21675117 + Missense_Mutation SNP G G A TCGA-37-4141-01A-02D-1352-08 TCGA-37-4141-10A-01D-1352-08 g.chrX:21675117G>A c.790C>T c.(790-792)Cgc>Tgc p.R264C LUSC 23 21675151 21675151 + Silent SNP G G A TCGA-66-2780-01A-01D-1522-08 TCGA-66-2780-11A-01D-1522-08 g.chrX:21675151G>A c.756C>T c.(754-756)atC>atT p.I252I LUSC 23 21675230 21675230 + Missense_Mutation SNP C C A TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chrX:21675230C>A c.677G>T c.(676-678)gGc>gTc p.G226V OV 23 21674169 21674169 + Missense_Mutation SNP T T G TCGA-23-1022-01A-02W-0488-09 TCGA-23-1022-10A-01W-0488-09 g.chrX:21674169T>G c.1738A>C c.(1738-1740)Aag>Cag p.K580Q PAAD 23 21674239 21674239 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:21674239C>T c.1668G>A c.(1666-1668)ccG>ccA p.P556P PAAD 23 21675080 21675080 + Missense_Mutation SNP C C T TCGA-US-A776-01A-13D-A33T-08 TCGA-US-A776-11A-11D-A33W-08 g.chrX:21675080C>T c.827G>A c.(826-828)cGg>cAg p.R276Q PAAD 23 21675171 21675171 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:21675171C>T c.736G>A c.(736-738)Gcc>Acc p.A246T PCPG 23 21674920 21674922 + In_Frame_Del DEL CTC CTC - TCGA-W2-A7HA-01B-11D-A35I-08 TCGA-W2-A7HA-10C-01D-A35G-08 g.chrX:21674920_21674922delCTC c.985_987delGAG c.(985-987)gagdel p.E329del READ 23 21674619 21674619 + Missense_Mutation SNP C C T TCGA-CL-5917-01A-11D-1657-10 TCGA-CL-5917-10A-01D-1657-10 g.chrX:21674619C>T c.1288G>A c.(1288-1290)Gtc>Atc p.V430I READ 23 21675045 21675046 + Frame_Shift_Ins INS - - C TCGA-AG-3727-01A-01W-0899-10 TCGA-AG-3727-10A-01W-0901-10 g.chrX:21675045_21675046insC c.861_862insG c.(859-864)gggcgcfs p.R288fs

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US X 21674920 21674922 deletion of <=200bp CTC - inframe_deletion E329 BLCA-US X 21675005 21675005 single base substitution G A missense_variant P301L 902C>T BLCA-US X 21675187 21675187 single base substitution A G synonymous_variant S240S 720T>C BOCA-FR X 21670176 21670176 single base substitution G T downstream_gene_variant BRCA-EU X 21669277 21669277 single base substitution C A downstream_gene_variant BRCA-EU X 21669575 21669575 single base substitution T A downstream_gene_variant BRCA-EU X 21670345 21670345 deletion of <=200bp T - downstream_gene_variant BRCA-EU X 21671474 21671474 insertion of <=200bp - TA downstream_gene_variant BRCA-EU X 21671492 21671492 single base substitution T A downstream_gene_variant BRCA-EU X 21672439 21672439 single base substitution G T downstream_gene_variant BRCA-EU X 21673128 21673128 single base substitution C T downstream_gene_variant BRCA-EU X 21674162 21674162 single base substitution C T missense_variant R582Q 1745G>A BRCA-EU X 21674383 21674383 single base substitution C T synonymous_variant K508K 1524G>A BRCA-EU X 21674588 21674588 single base substitution A G missense_variant L440P 1319T>C BRCA-EU X 21676463 21676463 deletion of <=200bp G - upstream_gene_variant BRCA-EU X 21676615 21676615 single base substitution C T upstream_gene_variant BRCA-EU X 21677300 21677300 single base substitution T A upstream_gene_variant BRCA-EU X 21677480 21677480 single base substitution C T upstream_gene_variant BRCA-EU X 21678158 21678158 single base substitution C A upstream_gene_variant BRCA-EU X 21680047 21680047 single base substitution C G upstream_gene_variant BRCA-EU X 21680476 21680476 single base substitution C G upstream_gene_variant BRCA-FR X 21671492 21671492 single base substitution T A downstream_gene_variant BRCA-FR X 21674263 21674263 single base substitution G A synonymous_variant A548A 1644C>T BRCA-FR X 21679869 21679869 single base substitution G A upstream_gene_variant BRCA-KR X 21675549 21675549 single base substitution G A missense_variant R120C 358C>T BRCA-UK X 21677480 21677480 single base substitution C T upstream_gene_variant BRCA-UK X 21680566 21680566 single base substitution C G upstream_gene_variant BRCA-US X 21670489 21670489 single base substitution A C downstream_gene_variant BRCA-US X 21670583 21670583 single base substitution G C downstream_gene_variant BRCA-US X 21674415 21674415 single base substitution C T missense_variant V498I 1492G>A BRCA-US X 21674481 21674481 deletion of <=200bp C - frameshift_variant V476 BRCA-US X 21675045 21675045 insertion of <=200bp - C frameshift_variant R288R? BRCA-US X 21675572 21675572 single base substitution G T missense_variant T112N 335C>A BTCA-JP X 21670527 21670527 single base substitution T G downstream_gene_variant BTCA-JP X 21674242 21674242 single base substitution C T synonymous_variant R555R 1665G>A BTCA-JP X 21674642 21674642 single base substitution G A missense_variant A422V 1265C>T BTCA-JP X 21674679 21674679 single base substitution C T missense_variant A410T 1228G>A BTCA-JP X 21675046 21675046 deletion of <=200bp C - frameshift_variant G287 CESC-US X 21670430 21670430 single base substitution G C downstream_gene_variant CESC-US X 21675600 21675600 single base substitution G A synonymous_variant L103L 307C>T CLLE-ES X 21673931 21673931 single base substitution G T 3_prime_UTR_variant CLLE-ES X 21677955 21677956 deletion of <=200bp TT - upstream_gene_variant COAD-US X 21674156 21674156 single base substitution G A missense_variant S584L 1751C>T COAD-US X 21674234 21674234 single base substitution G T missense_variant P558H 1673C>A COAD-US X 21674283 21674283 single base substitution C T missense_variant E542K 1624G>A COAD-US X 21674284 21674284 single base substitution G A synonymous_variant I541I 1623C>T COAD-US X 21674690 21674690 single base substitution G A missense_variant T406M 1217C>T COAD-US X 21674707 21674707 single base substitution C T synonymous_variant P400P 1200G>A COAD-US X 21674812 21674812 single base substitution G T synonymous_variant G365G 1095C>A COAD-US X 21675046 21675046 deletion of <=200bp C - frameshift_variant G287 COAD-US X 21675080 21675080 single base substitution C T missense_variant R276Q 827G>A COAD-US X 21675338 21675338 single base substitution C T missense_variant R190Q 569G>A COAD-US X 21675345 21675345 single base substitution C T missense_variant V188M 562G>A COAD-US X 21675634 21675634 single base substitution C T stop_gained W91* 273G>A COAD-US X 21675704 21675704 single base substitution C T missense_variant R68H 203G>A COAD-US X 21675868 21675868 single base substitution G A synonymous_variant G13G 39C>T COCA-CN X 21674279 21674279 single base substitution C T missense_variant R543H 1628G>A COCA-CN X 21674363 21674363 single base substitution G A missense_variant A515V 1544C>T COCA-CN X 21674617 21674617 single base substitution G A synonymous_variant V430V 1290C>T COCA-CN X 21674643 21674643 single base substitution C T missense_variant A422T 1264G>A COCA-CN X 21674983 21674983 single base substitution C T synonymous_variant Q308Q 924G>A COCA-CN X 21675110 21675110 single base substitution G A missense_variant P266L 797C>T COCA-CN X 21675627 21675627 single base substitution G A missense_variant L94F 280C>T COCA-CN X 21675641 21675641 single base substitution G T missense_variant T89N 266C>A COCA-CN X 21675707 21675707 single base substitution G A missense_variant A67V 200C>T COCA-CN X 21675834 21675834 single base substitution C T missense_variant E25K 73G>A ESCA-CN X 21674200 21674200 single base substitution G A synonymous_variant V569V 1707C>T ESCA-CN X 21675758 21675758 single base substitution G C missense_variant S50C 149C>G GBM-US X 21674007 21674007 single base substitution C T missense_variant E634K 1900G>A GBM-US X 21674666 21674666 single base substitution G A missense_variant A414V 1241C>T GBM-US X 21675201 21675201 single base substitution C T missense_variant V236M 706G>A GBM-US X 21675213 21675213 single base substitution C G missense_variant V232L 694G>C GBM-US X 21675508 21675508 single base substitution G A synonymous_variant F133F 399C>T KIRC-US X 21674384 21674384 deletion of <=200bp T - frameshift_variant K508 KIRC-US X 21674907 21674907 single base substitution G T missense_variant Q334K 1000C>A LGG-US X 21674920 21674922 deletion of <=200bp CTC - inframe_deletion E329 LICA-FR X 21674497 21674497 single base substitution G T synonymous_variant V470V 1410C>A LICA-FR X 21675313 21675313 single base substitution G A synonymous_variant G198G 594C>T LICA-FR X 21675674 21675674 single base substitution G A missense_variant A78V 233C>T LIHC-US X 21675562 21675562 single base substitution C T synonymous_variant L115L 345G>A LINC-JP X 21675345 21675345 single base substitution C T missense_variant V188M 562G>A LINC-JP X 21675965 21675965 single base substitution G C 5_prime_UTR_variant LINC-JP X 21676247 21676247 single base substitution G T 5_prime_UTR_variant LIRI-JP X 21669793 21669793 single base substitution A G downstream_gene_variant LIRI-JP X 21672979 21672979 single base substitution C T downstream_gene_variant LIRI-JP X 21674776 21674776 single base substitution G A synonymous_variant S377S 1131C>T LIRI-JP X 21677656 21677656 single base substitution T A upstream_gene_variant LIRI-JP X 21679647 21679647 single base substitution G A upstream_gene_variant LIRI-JP X 21680619 21680619 single base substitution T C upstream_gene_variant LIRI-JP X 21681377 21681377 single base substitution G A upstream_gene_variant LUSC-KR X 21670465 21670465 single base substitution C G downstream_gene_variant LUSC-KR X 21674141 21674141 single base substitution G A missense_variant T589I 1766C>T LUSC-KR X 21674485 21674485 single base substitution A T synonymous_variant G474G 1422T>A LUSC-KR X 21680671 21680671 single base substitution C T upstream_gene_variant LUSC-US X 21670577 21670577 single base substitution G A downstream_gene_variant LUSC-US X 21674689 21674689 single base substitution C A synonymous_variant T406T 1218G>T LUSC-US X 21675117 21675117 single base substitution G A missense_variant R264C 790C>T LUSC-US X 21675151 21675151 single base substitution G A synonymous_variant I252I 756C>T LUSC-US X 21675230 21675230 single base substitution C A missense_variant G226V 677G>T MALY-DE X 21670688 21670688 single base substitution G T downstream_gene_variant MALY-DE X 21677262 21677262 single base substitution T C upstream_gene_variant MALY-DE X 21677693 21677693 single base substitution A G upstream_gene_variant MALY-DE X 21679619 21679619 single base substitution C A upstream_gene_variant MALY-DE X 21681169 21681169 insertion of <=200bp - A upstream_gene_variant MELA-AU X 21669318 21669318 single base substitution G A downstream_gene_variant MELA-AU X 21669344 21669344 single base substitution G A downstream_gene_variant MELA-AU X 21669554 21669554 single base substitution C G downstream_gene_variant MELA-AU X 21669669 21669669 single base substitution C T downstream_gene_variant MELA-AU X 21669897 21669897 single base substitution G T downstream_gene_variant MELA-AU X 21670501 21670501 single base substitution G A downstream_gene_variant MELA-AU X 21670768 21670769 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU X 21670804 21670804 single base substitution A C downstream_gene_variant MELA-AU X 21671824 21671824 single base substitution G A downstream_gene_variant MELA-AU X 21671886 21671886 single base substitution G A downstream_gene_variant MELA-AU X 21672100 21672100 single base substitution A T downstream_gene_variant MELA-AU X 21672579 21672579 single base substitution G A downstream_gene_variant MELA-AU X 21673366 21673366 single base substitution C T downstream_gene_variant MELA-AU X 21673514 21673514 single base substitution G A downstream_gene_variant MELA-AU X 21673776 21673791 deletion of <=200bp CCCCCCGCCCCGCTGT - 3_prime_UTR_variant MELA-AU X 21674540 21674540 single base substitution G A missense_variant A456V 1367C>T MELA-AU X 21674758 21674759 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P383L 1148CC>TT MELA-AU X 21675279 21675279 single base substitution T G missense_variant T210P 628A>C MELA-AU X 21675430 21675430 single base substitution C T synonymous_variant Q159Q 477G>A MELA-AU X 21677233 21677233 single base substitution C T upstream_gene_variant MELA-AU X 21677607 21677608 multiple base substitution (>=2bp and <=200bp) AT TA upstream_gene_variant MELA-AU X 21677660 21677660 single base substitution C T upstream_gene_variant MELA-AU X 21677936 21677936 single base substitution G T upstream_gene_variant MELA-AU X 21678054 21678054 single base substitution G A upstream_gene_variant MELA-AU X 21678990 21678990 single base substitution C T upstream_gene_variant MELA-AU X 21679761 21679761 single base substitution G A upstream_gene_variant MELA-AU X 21680736 21680736 single base substitution C T upstream_gene_variant MELA-AU X 21680800 21680800 single base substitution C T upstream_gene_variant MELA-AU X 21680942 21680942 single base substitution T C upstream_gene_variant ORCA-IN X 21674053 21674053 single base substitution G A synonymous_variant C618C 1854C>T ORCA-IN X 21674450 21674450 single base substitution C T missense_variant G486D 1457G>A ORCA-IN X 21674515 21674515 single base substitution G A synonymous_variant H464H 1392C>T ORCA-IN X 21675027 21675027 single base substitution C T missense_variant V294M 880G>A ORCA-IN X 21675326 21675326 single base substitution G T missense_variant A194D 581C>A ORCA-IN X 21679763 21679763 single base substitution G T upstream_gene_variant OV-AU X 21674790 21674790 single base substitution C G missense_variant G373R 1117G>C OV-US X 21674169 21674169 single base substitution T G missense_variant K580Q 1738A>C PACA-AU X 21673130 21673130 single base substitution G C downstream_gene_variant PACA-AU X 21673900 21673900 single base substitution C T 3_prime_UTR_variant PACA-AU X 21676151 21676151 single base substitution C T 5_prime_UTR_variant PACA-AU X 21677628 21677628 single base substitution A T upstream_gene_variant PACA-AU X 21677703 21677703 single base substitution C A upstream_gene_variant PACA-AU X 21677704 21677704 single base substitution T G upstream_gene_variant PACA-AU X 21681062 21681062 single base substitution C A upstream_gene_variant PACA-CA X 21672180 21672180 single base substitution G T downstream_gene_variant PACA-CA X 21674283 21674283 single base substitution C T missense_variant E542K 1624G>A PACA-CA X 21675046 21675046 deletion of <=200bp C - frameshift_variant G287 PACA-CA X 21675243 21675243 single base substitution G A missense_variant R222C 664C>T PACA-CA X 21675348 21675348 single base substitution C T missense_variant D187N 559G>A PACA-CA X 21675838 21675838 single base substitution G A synonymous_variant R23R 69C>T PAEN-IT X 21673709 21673709 single base substitution C T 3_prime_UTR_variant PBCA-DE X 21669621 21669621 single base substitution T A downstream_gene_variant PBCA-DE X 21671474 21671474 insertion of <=200bp - TA downstream_gene_variant PRAD-UK X 21675128 21675128 single base substitution G A missense_variant T260M 779C>T READ-US X 21674619 21674619 single base substitution C T missense_variant V430I 1288G>A RECA-EU X 21677244 21677244 single base substitution T C upstream_gene_variant SKCA-BR X 21675445 21675445 single base substitution G A synonymous_variant I154I 462C>T SKCM-US X 21675792 21675792 single base substitution C T missense_variant E39K 115G>A STAD-US X 21670583 21670583 single base substitution G C downstream_gene_variant STAD-US X 21670629 21670629 single base substitution C T downstream_gene_variant STAD-US X 21674083 21674083 single base substitution C T synonymous_variant A608A 1824G>A STAD-US X 21674117 21674117 single base substitution A T missense_variant L597H 1790T>A STAD-US X 21674200 21674200 single base substitution G A synonymous_variant V569V 1707C>T STAD-US X 21674642 21674642 single base substitution G A missense_variant A422V 1265C>T STAD-US X 21674964 21674964 single base substitution C T missense_variant E315K 943G>A STAD-US X 21675116 21675116 single base substitution C T missense_variant R264H 791G>A STAD-US X 21675213 21675213 single base substitution C T missense_variant V232I 694G>A STAD-US X 21675537 21675537 single base substitution G A missense_variant R124C 370C>T STAD-US X 21675792 21675792 single base substitution C T missense_variant E39K 115G>A STAD-US X 21675868 21675868 single base substitution G A synonymous_variant G13G 39C>T STAD-US X 21675899 21675899 single base substitution T C missense_variant Y3C 8A>G UCEC-US X 21674198 21674198 single base substitution T G missense_variant E570A 1709A>C UCEC-US X 21674364 21674364 single base substitution C T missense_variant A515T 1543G>A UCEC-US X 21674883 21674883 single base substitution A G missense_variant Y342H 1024T>C UCEC-US X 21675201 21675201 single base substitution C T missense_variant V236M 706G>A UCEC-US X 21675206 21675206 single base substitution C T missense_variant R234Q 701G>A UCEC-US X 21675213 21675213 single base substitution C T missense_variant V232I 694G>A UCEC-US X 21675237 21675237 single base substitution G A missense_variant R224C 670C>T UCEC-US X 21675704 21675704 single base substitution C T missense_variant R68H 203G>A UCEC-US X 21675715 21675715 single base substitution T A missense_variant E64D 192A>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 587228 COSM1212651 c.1244G>A p.R415Q Substitution - Missense 23:21656545-21656545 - B100 COSM1467217 c.985_987delGAG p.E329delE Deletion - In frame 23:21656802-21656804 - T13 COSM5617841 c.1733G>T p.G578V Substitution - Missense 23:21656056-21656056 - TCGA-DS-A0VM-01 COSM462260 c.307C>T p.L103L Substitution - coding silent 23:21657482-21657482 - TCGA-BR-6852-01 COSM1255985 c.943G>A p.E315K Substitution - Missense 23:21656846-21656846 - T3091 COSM4696534 c.1718C>T p.A573V Substitution - Missense 23:21656071-21656071 - T2991 COSM4696537 c.1320G>T p.L440L Substitution - coding silent 23:21656469-21656469 - OSCC-GB_00590111 COSM4888636 c.1392C>T p.H464H Substitution - coding silent 23:21656397-21656397 - I2L-P24Tb-Tumor-Biopsy COSM5367271 c.613C>T p.R205W Substitution - Missense 23:21657176-21657176 - 587224 COSM1212652 c.568C>T p.R190W Substitution - Missense 23:21657221-21657221 - T2284 COSM4696532 c.1802G>A p.R601H Substitution - Missense 23:21655987-21655987 - CHC892T COSM4797172 c.594C>T p.G198G Substitution - coding silent 23:21657195-21657195 - TCGA-A6-5665-01 COSM1467218 c.861delG p.R288fs*7 Deletion - Frameshift 23:21656928-21656928 - BD217T COSM5495503 c.1665G>A p.R555R Substitution - coding silent 23:21656124-21656124 - TCGA-06-2558 COSM1119175 c.706G>A p.V236M Substitution - Missense 23:21657083-21657083 - TCGA-28-6450-01 COSM3406229 c.399C>T p.F133F Substitution - coding silent 23:21657390-21657390 - TCGA-CG-5733-01 COSM1119179 c.694G>A p.V232I Substitution - Missense 23:21657095-21657095 - TCGA-D5-6927-01 COSM1467212 c.1673C>A p.P558H Substitution - Missense 23:21656116-21656116 - Pat_22_B COSM4696533 c.1769G>A p.R590H Substitution - Missense 23:21656020-21656020 - ESCC_112 COSM5639552 c.1399G>A p.A467T Substitution - Missense 23:21656390-21656390 - TCGA-D5-6533-01 COSM1467220 c.569G>A p.R190Q Substitution - Missense 23:21657220-21657220 - TCGA-66-2759-01 COSM756540 c.677G>T p.G226V Substitution - Missense 23:21657112-21657112 - Pat_45_A COSM5877620 c.107A>G p.E36G Substitution - Missense 23:21657682-21657682 - TCGA-CJ-6032-01 COSM488248 c.1000C>A p.Q334K Substitution - Missense 23:21656789-21656789 - Gp2D COSM4629009 c.356G>T p.G119V Substitution - Missense 23:21657433-21657433 - TCGA-BR-8361-01 COSM4108613 c.370C>T p.R124C Substitution - Missense 23:21657419-21657419 - TCGA-G4-6322-01 COSM3694502 c.562G>A p.V188M Substitution - Missense 23:21657227-21657227 - TCGA-AP-A054-01 COSM1119173 c.1024T>C p.Y342H Substitution - Missense 23:21656765-21656765 - TCGA-19-1390-01 COSM3406227 c.1900G>A p.E634K Substitution - Missense 23:21655889-21655889 - ESO-K08 COSM1255986 c.105C>T p.T35T Substitution - coding silent 23:21657684-21657684 - TCGA-D1-A15X-01 COSM1119187 c.192A>T p.E64D Substitution - Missense 23:21657597-21657597 - HCT15 COSM4626550 c.87C>T p.C29C Substitution - coding silent 23:21657702-21657702 - sysucc-1128T COSM5469262 c.1264G>A p.A422T Substitution - Missense 23:21656525-21656525 - CHC892T COSM4797172 c.594C>T p.G198G Substitution - coding silent 23:21657195-21657195 - ESO-107 COSM1255984 c.630T>G p.T210T Substitution - coding silent 23:21657159-21657159 - TCGA-EW-A1OY-01 COSM1239281 c.1492G>A p.V498I Substitution - Missense 23:21656297-21656297 - TCGA-06-2558-01 COSM1119175 c.706G>A p.V236M Substitution - Missense 23:21657083-21657083 - PD9589a COSM5769759 c.1745G>A p.R582Q Substitution - Missense 23:21656044-21656044 - TCGA-DM-A0XF-01 COSM1467215 c.1200G>A p.P400P Substitution - coding silent 23:21656589-21656589 - TCGA-BR-6452-01 COSM3560384 c.115G>A p.E39K Substitution - Missense 23:21657674-21657674 - CHC892T COSM4797251 c.233C>T p.A78V Substitution - Missense 23:21657556-21657556 - OSCC-GB_00650111 COSM4890424 c.581C>A p.A194D Substitution - Missense 23:21657208-21657208 - 394 COSM4428609 c.842G>A p.R281H Substitution - Missense 23:21656947-21656947 - TCGA-23-1022-01 COSM75169 c.1738A>C p.K580Q Substitution - Missense 23:21656051-21656051 - CHEWS015 COSM4589378 c.686C>T p.P229L Substitution - Missense 23:21657103-21657103 - TCGA-AO-A03R-01 COSM256139 c.861_862insG p.R288fs*9 Insertion - Frameshift 23:21656927-21656928 - 2_RESISTANT COSM1467217 c.985_987delGAG p.E329delE Deletion - In frame 23:21656802-21656804 - S01578 COSM5670750 c.417G>T p.A139A Substitution - coding silent 23:21657372-21657372 - I2L-P24Ta-Tumor-Biopsy COSM5367251 c.1417C>T p.R473C Substitution - Missense 23:21656372-21656372 - RK308_C01 COSM3747414 c.1131C>T p.S377S Substitution - coding silent 23:21656658-21656658 - OSCC-GB_01250111 COSM5954755 c.1457G>A p.G486D Substitution - Missense 23:21656332-21656332 - S02255 COSM5681103 c.268G>T p.A90S Substitution - Missense 23:21657521-21657521 - TCGA-AN-A0FN-01 COSM5835925 c.1426delG p.V476fs*117 Deletion - Frameshift 23:21656363-21656363 - PTC-7C COSM4156775 c.872G>T p.R291L Substitution - Missense 23:21656917-21656917 - TCGA-D7-6522-01 COSM4108610 c.1707C>T p.V569V Substitution - coding silent 23:21656082-21656082 - NCI-H720 COSM5368296 c.1247C>G p.A416G Substitution - Missense 23:21656542-21656542 - T231 COSM4696539 c.1159G>A p.D387N Substitution - Missense 23:21656630-21656630 - SNU-175 COSM3036537 c.279G>A p.S93S Substitution - coding silent 23:21657510-21657510 - ESO-045 COSM1255982 c.567G>A p.A189A Substitution - coding silent 23:21657222-21657222 - pfg016T COSM1644001 c.703C>T p.R235C Substitution - Missense 23:21657086-21657086 - HCT116 COSM4632515 c.783G>A p.T261T Substitution - coding silent 23:21657006-21657006 - TCGA-AG-3727-01 COSM256139 c.861_862insG p.R288fs*9 Insertion - Frameshift 23:21656927-21656928 - 1 COSM1716145 c.839C>G p.T280S Substitution - Missense 23:21656950-21656950 - Gp5D COSM3036541 c.80T>C p.F27S Substitution - Missense 23:21657709-21657709 - TCGA-HU-A4GX-01 COSM4108614 c.8A>G p.Y3C Substitution - Missense 23:21657781-21657781 - CHC320T COSM3668709 c.1410C>A p.V470V Substitution - coding silent 23:21656379-21656379 - TCGA-HU-A4GC-01 COSM1467222 c.39C>T p.G13G Substitution - coding silent 23:21657750-21657750 - TCGA-BR-6452-01 COSM4108612 c.791G>A p.R264H Substitution - Missense 23:21656998-21656998 - OSCC-GB_00730111 COSM4888954 c.880G>A p.V294M Substitution - Missense 23:21656909-21656909 - S02328 COSM5692278 c.25A>G p.K9E Substitution - Missense 23:21657764-21657764 - Gp5D COSM4629008 c.782C>T p.T261M Substitution - Missense 23:21657007-21657007 - S02255 COSM5681102 c.554C>G p.A185G Substitution - Missense 23:21657235-21657235 - AOCS-145-1-6 COSM4137815 c.1117G>C p.G373R Substitution - Missense 23:21656672-21656672 - TCGA-A8-A07I-01 COSM457245 c.335C>A p.T112N Substitution - Missense 23:21657454-21657454 - ESO-859 COSM1239281 c.1492G>A p.V498I Substitution - Missense 23:21656297-21656297 - C086 COSM5533477 c.1533C>T p.P511P Substitution - coding silent 23:21656256-21656256 - 2492724 COSM5725256 c.760C>T p.Q254* Substitution - Nonsense 23:21657029-21657029 - TCGA-B5-A0K9-01 COSM1119171 c.1543G>A p.A515T Substitution - Missense 23:21656246-21656246 - TCGA-D1-A17D-01 COSM1119183 c.670C>T p.R224C Substitution - Missense 23:21657119-21657119 - T407 COSM4696535 c.1551C>T p.F517F Substitution - coding silent 23:21656238-21656238 - TCGA-DM-A1DA-01 COSM1467219 c.827G>A p.R276Q Substitution - Missense 23:21656962-21656962 - CRC-35T COSM5468852 c.797C>T p.P266L Substitution - Missense 23:21656992-21656992 - TCGA-BS-A0TJ-01 COSM1119175 c.706G>A p.V236M Substitution - Missense 23:21657083-21657083 - YUROS COSM5412443 c.1800C>T p.D600D Substitution - coding silent 23:21655989-21655989 - TCGA-66-2763-01 COSM756543 c.1218G>T p.T406T Substitution - coding silent 23:21656571-21656571 - 2492726 COSM5725256 c.760C>T p.Q254* Substitution - Nonsense 23:21657029-21657029 - TCGA-AP-A0LD-01 COSM1119169 c.1709A>C p.E570A Substitution - Missense 23:21656080-21656080 - BK0043 COSM4187625 c.1810G>A p.D604N Substitution - Missense 23:21655979-21655979 - C135 COSM4618917 c.463G>A p.V155M Substitution - Missense 23:21657326-21657326 - T55 COSM4696541 c.513C>A p.L171L Substitution - coding silent 23:21657276-21657276 - sysucc-863T COSM5765190 c.1290C>T p.V430V Substitution - coding silent 23:21656499-21656499 - ESCC_BICR_070T COSM5445210 c.149C>G p.S50C Substitution - Missense 23:21657640-21657640 - 587332 COSM1212653 c.700C>T p.R234W Substitution - Missense 23:21657089-21657089 - TCGA-AA-3502-01 COSM1467214 c.1623C>T p.I541I Substitution - coding silent 23:21656166-21656166 - KPOPBR-27-T COSM5966052 c.358C>T p.R120C Substitution - Missense 23:21657431-21657431 - 61 COSM5476908 c.1628G>A p.R543H Substitution - Missense 23:21656161-21656161 - U251 COSM1682444 c.261C>G p.I87M Substitution - Missense 23:21657528-21657528 - Pat_06_A COSM5877619 c.671G>A p.R224H Substitution - Missense 23:21657118-21657118 - 14T COSM3713888 c.1854C>T p.C618C Substitution - coding silent 23:21655935-21655935 - 2492726 COSM5725335 c.813G>A p.E271E Substitution - coding silent 23:21656976-21656976 - S02139 COSM5674717 c.1361C>A p.T454K Substitution - Missense 23:21656428-21656428 - DLD1 COSM4626550 c.87C>T p.C29C Substitution - coding silent 23:21657702-21657702 - CSCC-45-T COSM4469984 c.1632C>G p.Y544* Substitution - Nonsense 23:21656157-21656157 - T3090 COSM4696543 c.90C>T p.D30D Substitution - coding silent 23:21657699-21657699 - sysucc-274T COSM5476909 c.1544C>T p.A515V Substitution - Missense 23:21656245-21656245 - TCGA-D1-A15Z-01 COSM1119181 c.693C>T p.D231D Substitution - coding silent 23:21657096-21657096 - OSCC-GB_00140111 COSM3713888 c.1854C>T p.C618C Substitution - coding silent 23:21655935-21655935 - BD236T COSM4108611 c.1265C>T p.A422V Substitution - Missense 23:21656524-21656524 - CSCC-10-T COSM4519393 c.1008G>A p.V336V Substitution - coding silent 23:21656781-21656781 - TCGA-CL-5917-01 COSM1570250 c.1288G>A p.V430I Substitution - Missense 23:21656501-21656501 - CCK81 COSM3036525 c.1821C>T p.C607C Substitution - coding silent 23:21655968-21655968 - TCGA-02-0055-01 COSM2149028 c.1241C>T p.A414V Substitution - Missense 23:21656548-21656548 - ESO-859 COSM1239280 c.1272C>T p.G424G Substitution - coding silent 23:21656517-21656517 - I2L-P24Ta-Tumor-Organoid COSM5367251 c.1417C>T p.R473C Substitution - Missense 23:21656372-21656372 - LUAD-CHTN-Z4716A COSM362685 c.735C>A p.P245P Substitution - coding silent 23:21657054-21657054 - TCGA-BT-A20J-01 COSM422609 c.902C>T p.P301L Substitution - Missense 23:21656887-21656887 - BD72T COSM1467218 c.861delG p.R288fs*7 Deletion - Frameshift 23:21656928-21656928 - CSCC-20-T COSM4589887 c.862_863insG p.R289fs*8 Insertion - Frameshift 23:21656926-21656927 - BD57T COSM5511248 c.1228G>A p.A410T Substitution - Missense 23:21656561-21656561 - T3079 COSM4696533 c.1769G>A p.R590H Substitution - Missense 23:21656020-21656020 - CHC892T COSM4797251 c.233C>T p.A78V Substitution - Missense 23:21657556-21657556 - SNU-175 COSM4650870 c.1573C>T p.R525C Substitution - Missense 23:21656216-21656216 - HCT15 COSM1557294 c.69C>A p.R23R Substitution - coding silent 23:21657720-21657720 - T3262 COSM4696538 c.1166G>T p.R389L Substitution - Missense 23:21656623-21656623 - 585258 COSM321286 c.890A>T p.E297V Substitution - Missense 23:21656899-21656899 - LUAD-NYU739 COSM376324 c.337G>A p.E113K Substitution - Missense 23:21657452-21657452 - ESCC_120 COSM5640482 c.1753C>T p.R585C Substitution - Missense 23:21656036-21656036 - 587284 COSM1212654 c.443A>G p.D148G Substitution - Missense 23:21657346-21657346 - PCSI_0287_Pa_P_526 COSM4807420 c.69C>T p.R23R Substitution - coding silent 23:21657720-21657720 - TCGA-D5-6541-01 COSM1467216 c.1095C>A p.G365G Substitution - coding silent 23:21656694-21656694 - TCGA-HU-A4G8-01 COSM4108611 c.1265C>T p.A422V Substitution - Missense 23:21656524-21656524 - TCGA-CK-4952-01 COSM1467213 c.1624G>A p.E542K Substitution - Missense 23:21656165-21656165 - LIM1899 COSM4640952 c.1091C>T p.A364V Substitution - Missense 23:21656698-21656698 - 0035_CRUK_PC_0035_T1_DNA COSM5423219 c.779C>T p.T260M Substitution - Missense 23:21657010-21657010 - ESO-718 COSM1255985 c.943G>A p.E315K Substitution - Missense 23:21656846-21656846 - tumor_4116738 COSM1161818 c.391T>A p.C131S Substitution - Missense 23:21657398-21657398 - KM12 COSM4639288 c.1773C>T p.N591N Substitution - coding silent 23:21656016-21656016 - TCGA-BH-A0DZ-01 COSM256139 c.861_862insG p.R288fs*9 Insertion - Frameshift 23:21656927-21656928 - S01020 COSM5701171 c.352_353insT p.C118fs*94 Insertion - Frameshift 23:21657436-21657437 - LUAD-B00416 COSM355488 c.617A>T p.Q206L Substitution - Missense 23:21657172-21657172 - TCGA-CG-4465-01 COSM4108609 c.1790T>A p.L597H Substitution - Missense 23:21655999-21655999 - ESCC_BICR_052T COSM4108610 c.1707C>T p.V569V Substitution - coding silent 23:21656082-21656082 - 2292386 COSM4610615 c.1477C>T p.L493F Substitution - Missense 23:21656312-21656312 - T3658 COSM4696536 c.1380G>A p.P460P Substitution - coding silent 23:21656409-21656409 - SC_9008 COSM5572737 c.1632C>T p.Y544Y Substitution - coding silent 23:21656157-21656157 - TCGA-AA-3818-01 COSM293949 c.561C>T p.D187D Substitution - coding silent 23:21657228-21657228 - PCSI_0112_Pa_P COSM1467213 c.1624G>A p.E542K Substitution - Missense 23:21656165-21656165 - TCGA-E7-A3Y1-01 COSM3800540 c.720T>C p.S240S Substitution - coding silent 23:21657069-21657069 - TCGA-AZ-6598-01 COSM1119185 c.203G>A p.R68H Substitution - Missense 23:21657586-21657586 - 745_T COSM3965045 c.1860G>A p.V620V Substitution - coding silent 23:21655929-21655929 - CSCC-44-T COSM4480958 c.246C>T p.R82R Substitution - coding silent 23:21657543-21657543 - TCGA-EB-A3Y6-01 COSM3560384 c.115G>A p.E39K Substitution - Missense 23:21657674-21657674 - TCGA-B5-A0JR-01 COSM1119189 c.67C>T p.R23C Substitution - Missense 23:21657722-21657722 - TCGA-76-4935-01 COSM3406228 c.694G>C p.V232L Substitution - Missense 23:21657095-21657095 - CSCC-27-T COSM4543517 c.339G>A p.E113E Substitution - coding silent 23:21657450-21657450 - sysucc-274T COSM5476908 c.1628G>A p.R543H Substitution - Missense 23:21656161-21656161 - 585260 COSM321287 c.200C>G p.A67G Substitution - Missense 23:21657589-21657589 - T3724 COSM4696540 c.787T>C p.S263P Substitution - Missense 23:21657002-21657002 - S00022 COSM5656574 c.1366G>A p.A456T Substitution - Missense 23:21656423-21656423 - HCC156T COSM3694502 c.562G>A p.V188M Substitution - Missense 23:21657227-21657227 - CCRF-CEM COSM1682443 c.1732G>A p.G578S Substitution - Missense 23:21656057-21656057 - CSCC-1-T COSM4589886 c.1228_1229insT p.A410fs*29 Insertion - Frameshift 23:21656560-21656561 - TCGA-CK-4950-01 COSM1212655 c.1217C>T p.T406M Substitution - Missense 23:21656572-21656572 - ESCC_156 COSM4696532 c.1802G>A p.R601H Substitution - Missense 23:21655987-21655987 - CRC-15T COSM5468659 c.266C>A p.T89N Substitution - Missense 23:21657523-21657523 - sysucc-1370T COSM5472863 c.200C>T p.A67V Substitution - Missense 23:21657589-21657589 - TCGA-G3-A25Y-01 COSM4917841 c.345G>A p.L115L Substitution - coding silent 23:21657444-21657444 - 585272 COSM321288 c.1582G>T p.V528L Substitution - Missense 23:21656207-21656207 - CHC320T COSM3668709 c.1410C>A p.V470V Substitution - coding silent 23:21656379-21656379 - TCGA-BS-A0TJ-01 COSM1119185 c.203G>A p.R68H Substitution - Missense 23:21657586-21657586 - TCGA-AU-6004-01 COSM1467218 c.861delG p.R288fs*7 Deletion - Frameshift 23:21656928-21656928 - TCGA-61-2008-01 COSM116405 c.1657C>G p.R553G Substitution - Missense 23:21656132-21656132 - GC_304T-GC_304N COSM4772852 c.584G>A p.R195Q Substitution - Missense 23:21657205-21657205 - TCGA-02-0055 COSM2149028 c.1241C>T p.A414V Substitution - Missense 23:21656548-21656548 - sysucc-880T COSM4696542 c.280C>T p.L94F Substitution - Missense 23:21657509-21657509 - 2218465 COSM4421335 c.129C>G p.H43Q Substitution - Missense 23:21657660-21657660 - ESO-1059 COSM1255983 c.771C>G p.N257K Substitution - Missense 23:21657018-21657018 - LUAD-B02594 COSM356529 c.1702G>A p.V568M Substitution - Missense 23:21656087-21656087 - 49M COSM5591560 c.410delT p.V137fs*19 Deletion - Frameshift 23:21657379-21657379 - Gp2D COSM4629008 c.782C>T p.T261M Substitution - Missense 23:21657007-21657007 - TCGA-AP-A0LM-01 COSM1119179 c.694G>A p.V232I Substitution - Missense 23:21657095-21657095 - TCGA-66-2780-01 COSM756541 c.756C>T p.I252I Substitution - coding silent 23:21657033-21657033 - TCGA-CM-6171-01 COSM1467221 c.273G>A p.W91* Substitution - Nonsense 23:21657516-21657516 - S02245 COSM5678671 c.1546C>A p.R516S Substitution - Missense 23:21656243-21656243 - SNU-175 COSM4650871 c.359G>A p.R120H Substitution - Missense 23:21657430-21657430 - 12924 COSM5616280 c.1801C>A p.R601S Substitution - Missense 23:21655988-21655988 - 61 COSM5742212 c.506C>T p.A169V Substitution - Missense 23:21657283-21657283 - TCGA-BR-4292-01 COSM4108608 c.1824G>A p.A608A Substitution - coding silent 23:21655965-21655965 - TCGA-37-4141-01 COSM756542 c.790C>T p.R264C Substitution - Missense 23:21656999-21656999 - TCGA-CK-5913-01 COSM1467211 c.1751C>T p.S584L Substitution - Missense 23:21656038-21656038 - HCC156 COSM3694502 c.562G>A p.V188M Substitution - Missense 23:21657227-21657227 - 587394 COSM1212655 c.1217C>T p.T406M Substitution - Missense 23:21656572-21656572 - HOP-92 COSM1682444 c.261C>G p.I87M Substitution - Missense 23:21657528-21657528 - TCGA-AP-A0LM-01 COSM1119177 c.701G>A p.R234Q Substitution - Missense 23:21657088-21657088 - ASHPC_0009_Pa_P COSM3786469 c.559G>A p.D187N Substitution - Missense 23:21657230-21657230 - Au1 COSM5596939 c.1188C>T p.H396H Substitution - coding silent 23:21656601-21656601 - TCGA-A6-5665-01 COSM1467222 c.39C>T p.G13G Substitution - coding silent 23:21657750-21657750 - 2492729 COSM5726114 c.681G>A p.L227L Substitution - coding silent 23:21657108-21657108 - 587306 COSM1212650 c.496G>A p.A166T Substitution - Missense 23:21657293-21657293 - T1154 COSM4696542 c.280C>T p.L94F Substitution - Missense 23:21657509-21657509 - LUAD-S01478 COSM405219 c.204_205delCG p.V69fs*44 Deletion - Frameshift 23:21657584-21657585 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.448572 Xp22.12

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F4V c.10T>G X 21675897 CM A C Synonymous p.T210T c.630T>G X 21675277 ESCA A G Missense p.Y342H c.1024T>C X 21674883 UCEC A T Missense p.C131S c.391T>A X 21675516 DLBCL A T Missense p.L597H c.1790T>A X 21674117 STAD C A Missense p.G226V c.677G>T X 21675230 LUSC C A Missense p.G241C c.721G>T X 21675186 HNSC C A Missense p.V528L c.1582G>T X 21674325 SCLC C A Synonymous p.T406T c.1218G>T X 21674689 LUSC C A Synonymous p.V361V c.1083G>T X 21674824 LUAD - C Frameshift p.R288Afs*9 c.861dupG X 21675046 COREAD C G Missense p.V232L c.694G>C X 21675213 GBM CG TC Missense p.D386N c.1155_1156delinsGA X 21674751 CM CTC - InFrameDeletion p.E329delE c.985_987delGAG X 21674920 LGG C T Missense p.A515T c.1543G>A X 21674364 UCEC C T Missense p.E315K c.943G>A X 21674964 ESCA C T Missense p.E315K c.943G>A X 21674964 STAD C T Missense p.E323K c.967G>A X 21674940 CM C T Missense p.E39K c.115G>A X 21675792 CM C T Missense p.E634K c.1900G>A X 21674007 GBM C T Missense p.R68H c.203G>A X 21675704 UCEC C T Missense p.V232I c.694G>A X 21675213 STAD C T Missense p.V236M c.706G>A X 21675201 GBM C T Missense p.V236M c.706G>A X 21675201 UCEC C T Missense p.V498I c.1492G>A X 21674415 ESCA C T Synonymous p.A189A c.567G>A X 21675340 ESCA C T Synonymous p.A608A c.1824G>A X 21674083 STAD G A Missense p.A414V c.1241C>T X 21674666 GBM G A Missense p.P301L c.902C>T X 21675005 BLCA G A Missense p.R224C c.670C>T X 21675237 UCEC G A Missense p.R235C c.703C>T X 21675204 STAD G A Missense p.R264C c.790C>T X 21675117 LUSC G A Missense p.R450W c.1348C>T X 21674559 LUAD G A Synonymous p.D187D c.561C>T X 21675346 COREAD G A Synonymous p.D386D c.1158C>T X 21674749 HNSC G A Synonymous p.D598D c.1794C>T X 21674113 LUAD G A Synonymous p.F133F c.399C>T X 21675508 GBM G A Synonymous p.F54F c.162C>T X 21675745 CM G A Synonymous p.G424G c.1272C>T X 21674635 ESCA G A Synonymous p.H417H c.1251C>T X 21674656 CM G A Synonymous p.I252I c.756C>T X 21675151 LUSC G A Synonymous p.T35T c.105C>T X 21675802 ESCA G A Synonymous p.T514T c.1542C>T X 21674365 COREAD G A Synonymous p.V569V c.1707C>T X 21674200 STAD G C Missense p.A67G c.200C>G X 21675707 SCLC G C Missense p.N257K c.771C>G X 21675136 ESCA G C Missense p.R205G c.613C>G X 21675294 HNSC G C Missense p.R553G c.1657C>G X 21674250 OV G - Frameshift p.L57Cfs*13 c.169delC X 21675738 COREAD G T Missense p.P400Q c.1199C>A X 21674708 HNSC G T Missense p.Q334K c.1000C>A X 21674907 RCCC G T Missense p.T112N c.335C>A X 21675572 BRCA G T Synonymous p.T62T c.186C>A X 21675721 LUAD T A Missense p.E297V c.890A>T X 21675017 SCLC T C Missense p.Y544C c.1631A>G X 21674276 LUAD T - Frameshift p.K508Rfs*85 c.1523delA X 21674384 RCCC T G Missense p.E570A c.1709A>C X 21674198 UCEC T G Missense p.K580Q c.1738A>C X 21674169 OV