Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 23 142967266 142967266 + Missense_Mutation SNP G G T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chrX:142967266G>T c.64G>T c.(64-66)Ggc>Tgc p.G22C BLCA 23 142967294 142967294 + Missense_Mutation SNP A A G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chrX:142967294A>G c.92A>G c.(91-93)aAc>aGc p.N31S BLCA 23 142967427 142967427 + Missense_Mutation SNP A A T TCGA-FD-A5BV-01A-11D-A26M-08 TCGA-FD-A5BV-10A-01D-A26K-08 g.chrX:142967427A>T c.225A>T c.(223-225)aaA>aaT p.K75N BRCA 23 142967229 142967229 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chrX:142967229C>G c.27C>G c.(25-27)atC>atG p.I9M CESC 23 142967284 142967284 + Missense_Mutation SNP G G A TCGA-C5-A1BE-01B-11D-A13W-08 TCGA-C5-A1BE-10A-01D-A13W-08 g.chrX:142967284G>A c.82G>A c.(82-84)Gat>Aat p.D28N COAD 23 142967242 142967242 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:142967242C>A c.40C>A c.(40-42)Cgt>Agt p.R14S COAD 23 142967300 142967300 + Missense_Mutation SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chrX:142967300G>A c.98G>A c.(97-99)cGt>cAt p.R33H COAD 23 142967366 142967366 + Missense_Mutation SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chrX:142967366G>A c.164G>A c.(163-165)cGt>cAt p.R55H COAD 23 142967377 142967377 + Missense_Mutation SNP C C G TCGA-AA-A017-01A-01W-A00E-09 TCGA-AA-A017-10A-01W-A00E-09 g.chrX:142967377C>G c.175C>G c.(175-177)Ctt>Gtt p.L59V COAD 23 142967451 142967451 + Silent SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chrX:142967451G>A c.249G>A c.(247-249)aaG>aaA p.K83K COAD 23 142967459 142967459 + Missense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:142967459G>T c.257G>T c.(256-258)aGa>aTa p.R86I COAD 23 142967515 142967515 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:142967515G>A c.313G>A c.(313-315)Gtt>Att p.V105I COADREAD 23 142967242 142967242 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:142967242C>A c.40C>A c.(40-42)Cgt>Agt p.R14S COADREAD 23 142967300 142967300 + Missense_Mutation SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chrX:142967300G>A c.98G>A c.(97-99)cGt>cAt p.R33H COADREAD 23 142967366 142967366 + Missense_Mutation SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chrX:142967366G>A c.164G>A c.(163-165)cGt>cAt p.R55H COADREAD 23 142967377 142967377 + Missense_Mutation SNP C C G TCGA-AA-A017-01A-01W-A00E-09 TCGA-AA-A017-10A-01W-A00E-09 g.chrX:142967377C>G c.175C>G c.(175-177)Ctt>Gtt p.L59V COADREAD 23 142967451 142967451 + Silent SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chrX:142967451G>A c.249G>A c.(247-249)aaG>aaA p.K83K COADREAD 23 142967459 142967459 + Missense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chrX:142967459G>T c.257G>T c.(256-258)aGa>aTa p.R86I COADREAD 23 142967459 142967459 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:142967459G>T c.257G>T c.(256-258)aGa>aTa p.R86I COADREAD 23 142967509 142967509 + Missense_Mutation SNP C C T TCGA-AG-A032-01A-01W-A00E-09 TCGA-AG-A032-10A-01W-A00E-09 g.chrX:142967509C>T c.307C>T c.(307-309)Cgc>Tgc p.R103C COADREAD 23 142967515 142967515 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:142967515G>A c.313G>A c.(313-315)Gtt>Att p.V105I ESCA 23 142967287 142967287 + Missense_Mutation SNP G G A TCGA-2H-A9GG-01A-11D-A37C-09 TCGA-2H-A9GG-11A-11D-A37F-09 g.chrX:142967287G>A c.85G>A c.(85-87)Gaa>Aaa p.E29K GBM 23 142967295 142967295 + Silent SNP C C T TCGA-19-5947-01A-11D-1696-08 TCGA-19-5947-11A-01D-1696-08 g.chrX:142967295C>T c.93C>T c.(91-93)aaC>aaT p.N31N GBM 23 142967366 142967366 + Missense_Mutation SNP G G A TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chrX:142967366G>A c.164G>A c.(163-165)cGt>cAt p.R55H GBM 23 142967428 142967428 + Missense_Mutation SNP A A G TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chrX:142967428A>G c.226A>G c.(226-228)Att>Gtt p.I76V GBM 23 142967486 142967487 + Missense_Mutation DNP AG AG TA TCGA-14-0871-01A-01W-0424-08 TCGA-14-0871-10A-01W-0424-08 g.chrX:142967486_142967487AG>TA c.284_285AG>TA c.(283-285)aAG>aTA p.K95I GBMLGG 23 142967238 142967238 + Silent SNP C C A TCGA-E1-A7YV-01A-11D-A34J-08 TCGA-E1-A7YV-10A-01D-A34M-08 g.chrX:142967238C>A c.36C>A c.(34-36)acC>acA p.T12T GBMLGG 23 142967295 142967295 + Silent SNP C C T TCGA-19-5947-01A-11D-1696-08 TCGA-19-5947-11A-01D-1696-08 g.chrX:142967295C>T c.93C>T c.(91-93)aaC>aaT p.N31N GBMLGG 23 142967366 142967366 + Missense_Mutation SNP G G A TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chrX:142967366G>A c.164G>A c.(163-165)cGt>cAt p.R55H GBMLGG 23 142967428 142967428 + Missense_Mutation SNP A A G TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chrX:142967428A>G c.226A>G c.(226-228)Att>Gtt p.I76V GBMLGG 23 142967486 142967487 + Missense_Mutation DNP AG AG TA TCGA-14-0871-01A-01W-0424-08 TCGA-14-0871-10A-01W-0424-08 g.chrX:142967486_142967487AG>TA c.284_285AG>TA c.(283-285)aAG>aTA p.K95I GBMLGG 23 142967509 142967509 + Missense_Mutation SNP C C T TCGA-TQ-A7RK-01A-11D-A33T-08 TCGA-TQ-A7RK-10A-01D-A33W-08 g.chrX:142967509C>T c.307C>T c.(307-309)Cgc>Tgc p.R103C HNSC 23 142967283 142967283 + Silent SNP A A G TCGA-CV-7102-01A-11D-2012-08 TCGA-CV-7102-10A-01D-2013-08 g.chrX:142967283A>G c.81A>G c.(79-81)ccA>ccG p.P27P HNSC 23 142967296 142967296 + Missense_Mutation SNP G G T TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chrX:142967296G>T c.94G>T c.(94-96)Gcc>Tcc p.A32S HNSC 23 142967322 142967322 + Silent SNP T T A TCGA-CV-7440-01A-11D-2129-08 TCGA-CV-7440-10A-01D-2129-08 g.chrX:142967322T>A c.120T>A c.(118-120)gcT>gcA p.A40A HNSC 23 142967437 142967437 + Missense_Mutation SNP C C A TCGA-D6-8568-01A-11D-2394-08 TCGA-D6-8568-10A-01D-2394-08 g.chrX:142967437C>A c.235C>A c.(235-237)Cca>Aca p.P79T HNSC 23 142967601 142967601 + Missense_Mutation SNP C C A TCGA-CV-7248-01A-11D-2012-08 TCGA-CV-7248-10A-01D-2013-08 g.chrX:142967601C>A c.399C>A c.(397-399)aaC>aaA p.N133K KIPAN 23 142967630 142967630 + Missense_Mutation SNP C C T TCGA-B4-5844-01A-11D-1669-08 TCGA-B4-5844-10A-01D-1669-08 g.chrX:142967630C>T c.428C>T c.(427-429)gCa>gTa p.A143V KIRC 23 142967630 142967630 + Missense_Mutation SNP C C T TCGA-B4-5844-01A-11D-1669-08 TCGA-B4-5844-10A-01D-1669-08 g.chrX:142967630C>T c.428C>T c.(427-429)gCa>gTa p.A143V LGG 23 142967238 142967238 + Silent SNP C C A TCGA-E1-A7YV-01A-11D-A34J-08 TCGA-E1-A7YV-10A-01D-A34M-08 g.chrX:142967238C>A c.36C>A c.(34-36)acC>acA p.T12T LGG 23 142967509 142967509 + Missense_Mutation SNP C C T TCGA-TQ-A7RK-01A-11D-A33T-08 TCGA-TQ-A7RK-10A-01D-A33W-08 g.chrX:142967509C>T c.307C>T c.(307-309)Cgc>Tgc p.R103C LUAD 23 142967263 142967263 + Missense_Mutation SNP C C T TCGA-78-7156-01A-11D-2036-08 TCGA-78-7156-10A-01D-2036-08 g.chrX:142967263C>T c.61C>T c.(61-63)Cct>Tct p.P21S LUAD 23 142967314 142967314 + Missense_Mutation SNP G G T TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chrX:142967314G>T c.112G>T c.(112-114)Gtc>Ttc p.V38F LUAD 23 142967318 142967318 + Missense_Mutation SNP T T A TCGA-17-Z033-01A-01W-0746-08 TCGA-17-Z033-11A-01W-0746-08 g.chrX:142967318T>A c.116T>A c.(115-117)aTt>aAt p.I39N LUAD 23 142967330 142967330 + Nonsense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chrX:142967330C>A c.128C>A c.(127-129)tCa>tAa p.S43* LUAD 23 142967421 142967421 + Missense_Mutation SNP G G A TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chrX:142967421G>A c.219G>A c.(217-219)atG>atA p.M73I LUAD 23 142967514 142967514 + Silent SNP A A T TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chrX:142967514A>T c.312A>T c.(310-312)acA>acT p.T104T LUAD 23 142967515 142967515 + Missense_Mutation SNP G G C TCGA-64-5779-01A-01D-1625-08 TCGA-64-5779-10A-01D-1625-08 g.chrX:142967515G>C c.313G>C c.(313-315)Gtt>Ctt p.V105L LUAD 23 142967530 142967530 + Missense_Mutation SNP C C G TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chrX:142967530C>G c.328C>G c.(328-330)Cag>Gag p.Q110E LUAD 23 142967545 142967545 + Missense_Mutation SNP G G T TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chrX:142967545G>T c.343G>T c.(343-345)Gct>Tct p.A115S LUAD 23 142967583 142967583 + Silent SNP G G T TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chrX:142967583G>T c.381G>T c.(379-381)gtG>gtT p.V127V LUAD 23 142967630 142967630 + Missense_Mutation SNP C C A TCGA-86-7955-01A-11D-2184-08 TCGA-86-7955-10A-01D-2184-08 g.chrX:142967630C>A c.428C>A c.(427-429)gCa>gAa p.A143E LUSC 23 142967238 142967238 + Silent SNP C C A TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chrX:142967238C>A c.36C>A c.(34-36)acC>acA p.T12T LUSC 23 142967473 142967473 + Missense_Mutation SNP A A T TCGA-33-4586-01A-01D-1441-08 TCGA-33-4586-11A-01D-1441-08 g.chrX:142967473A>T c.271A>T c.(271-273)Att>Ttt p.I91F LUSC 23 142967551 142967551 + Missense_Mutation SNP A A C TCGA-46-3768-01A-01D-0983-08 TCGA-46-3768-10A-01D-0983-08 g.chrX:142967551A>C c.349A>C c.(349-351)Aat>Cat p.N117H LUSC 23 142967583 142967583 + Silent SNP G G A TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chrX:142967583G>A c.381G>A c.(379-381)gtG>gtA p.V127V LUSC 23 142967583 142967583 + Silent SNP G G A TCGA-51-4081-01A-01D-1458-08 TCGA-51-4081-11A-01D-1458-08 g.chrX:142967583G>A c.381G>A c.(379-381)gtG>gtA p.V127V LUSC 23 142967587 142967587 + Missense_Mutation SNP C C G TCGA-43-6770-01A-11D-1817-08 TCGA-43-6770-11A-01D-1817-08 g.chrX:142967587C>G c.385C>G c.(385-387)Cag>Gag p.Q129E PAAD 23 142967510 142967510 + Missense_Mutation SNP G G A TCGA-HZ-8637-01A-11D-2396-08 TCGA-HZ-8637-10A-01D-2396-08 g.chrX:142967510G>A c.308G>A c.(307-309)cGc>cAc p.R103H READ 23 142967459 142967459 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:142967459G>T c.257G>T c.(256-258)aGa>aTa p.R86I READ 23 142967509 142967509 + Missense_Mutation SNP C C T TCGA-AG-A032-01A-01W-A00E-09 TCGA-AG-A032-10A-01W-A00E-09 g.chrX:142967509C>T c.307C>T c.(307-309)Cgc>Tgc p.R103C SKCM 23 142967209 142967209 + Missense_Mutation SNP G G A TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chrX:142967209G>A c.7G>A c.(7-9)Gag>Aag p.E3K SKCM 23 142967226 142967226 + Silent SNP C C T TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chrX:142967226C>T c.24C>T c.(22-24)atC>atT p.I8I SKCM 23 142967308 142967308 + Missense_Mutation SNP C C T TCGA-EE-A29P-06A-11D-A197-08 TCGA-EE-A29P-10A-01D-A199-08 g.chrX:142967308C>T c.106C>T c.(106-108)Cat>Tat p.H36Y SKCM 23 142967308 142967308 + Missense_Mutation SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chrX:142967308C>T c.106C>T c.(106-108)Cat>Tat p.H36Y SKCM 23 142967326 142967326 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chrX:142967326G>A c.124G>A c.(124-126)Gaa>Aaa p.E42K SKCM 23 142967418 142967418 + Silent SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chrX:142967418C>T c.216C>T c.(214-216)ttC>ttT p.F72F SKCM 23 142967434 142967434 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chrX:142967434C>T c.232C>T c.(232-234)Cat>Tat p.H78Y SKCM 23 142967459 142967459 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chrX:142967459G>A c.257G>A c.(256-258)aGa>aAa p.R86K SKCM 23 142967493 142967493 + Silent SNP C C T TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chrX:142967493C>T c.291C>T c.(289-291)tcC>tcT p.S97S SKCM 23 142967526 142967526 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:142967526G>A c.324G>A c.(322-324)tcG>tcA p.S108S SKCM 23 142967602 142967602 + Missense_Mutation SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chrX:142967602G>A c.400G>A c.(400-402)Gaa>Aaa p.E134K

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-43-6770-01 COSM756052 c.385C>G p.Q129E Substitution - Missense 23:143884485-143884485 + TCGA-06-0649-01 COSM2151468 c.226A>G p.I76V Substitution - Missense 23:143884326-143884326 + 587338 COSM1231545 c.292C>A p.P98T Substitution - Missense 23:143884392-143884392 + CN-AML-NR-08-Dx COSM5000704 c.266T>G p.L89* Substitution - Nonsense S00539 COSM316327 c.211C>G p.R71G Substitution - Missense 23:143884311-143884311 + CSCC-60-T COSM4490860 c.36C>T p.T12T Substitution - coding silent 23:143884136-143884136 + S00539 COSM316327 c.211C>G p.R71G Substitution - Missense 23:143884311-143884311 + 049T COSM1729898 c.282T>A p.D94E Substitution - Missense 23:143884382-143884382 + TCGA-19-5947 COSM2156517 c.93C>T p.N31N Substitution - coding silent 23:143884193-143884193 + TCGA-EE-A29P-06 COSM3558847 c.106C>T p.H36Y Substitution - Missense 23:143884206-143884206 + TCGA-06-0649-01 COSM267711 c.164G>A p.R55H Substitution - Missense 23:143884264-143884264 + SJRHB059R COSM3737819 c.190C>G p.P64A Substitution - Missense 23:143884290-143884290 + P09-649 COSM248177 c.61C>G p.P21A Substitution - Missense 23:143884161-143884161 + J73_T COSM3964825 c.37C>G p.Q13E Substitution - Missense 23:143884137-143884137 + TCGA-FW-A3R5-06 COSM3913511 c.324G>A p.S108S Substitution - coding silent 23:143884424-143884424 + CHC1211T COSM4954843 c.94G>T p.A32S Substitution - Missense 23:143884194-143884194 + TCGA-AC-A23H-01 COSM3843781 c.27C>G p.I9M Substitution - Missense 23:143884127-143884127 + T578 COSM4738690 c.136T>C p.S46P Substitution - Missense 23:143884236-143884236 + PDA_101 COSM5000704 c.266T>G p.L89* Substitution - Nonsense TCGA-AA-3672-01 COSM267711 c.164G>A p.R55H Substitution - Missense 23:143884264-143884264 + S02322 COSM5691650 c.151G>T p.G51W Substitution - Missense 23:143884251-143884251 + TCGA-EE-A3AE-06 COSM1242976 c.216C>T p.F72F Substitution - coding silent 23:143884316-143884316 + TCGA-HU-A4GU-01 COSM4107230 c.414T>A p.I138I Substitution - coding silent 23:143884514-143884514 + T3724 COSM4738689 c.117T>C p.I39I Substitution - coding silent 23:143884217-143884217 + TCGA-HU-A4GU-01 COSM4107227 c.297C>A p.A99A Substitution - coding silent 23:143884397-143884397 + S01494 COSM316328 c.199G>A p.A67T Substitution - Missense 23:143884299-143884299 + TCGA-EE-A29L-06 COSM318254 c.124G>A p.E42K Substitution - Missense 23:143884224-143884224 + C086 COSM5541263 c.69C>T p.I23I Substitution - coding silent 23:143884169-143884169 + PT21_2 COSM3558847 c.106C>T p.H36Y Substitution - Missense 23:143884206-143884206 + ESO-632 COSM1269626 c.237A>C p.P79P Substitution - coding silent 23:143884337-143884337 + TCGA-DA-A3F8-06 COSM1715717 c.400G>A p.E134K Substitution - Missense 23:143884500-143884500 + S02139 COSM5674701 c.33A>T p.E11D Substitution - Missense 23:143884133-143884133 + TCGA-C5-A1BE-01 COSM4841404 c.82G>A p.D28N Substitution - Missense 23:143884182-143884182 + TCGA-19-5947-01 COSM2156517 c.93C>T p.N31N Substitution - coding silent 23:143884193-143884193 + TCGA-HU-A4GU-01 COSM4107231 c.455G>A p.S152N Substitution - Missense 23:143884555-143884555 + TCGA-EE-A2MD-06 COSM3558846 c.24C>T p.I8I Substitution - coding silent 23:143884124-143884124 + ZZUFHECRKL-G016T COSM5440223 c.153G>A p.G51G Substitution - coding silent 23:143884253-143884253 + 1286T COSM5762815 c.314T>A p.V105D Substitution - Missense 23:143884414-143884414 + PCSI_0623_Pa_P_526 COSM4137721 c.124G>T p.E42* Substitution - Nonsense 23:143884224-143884224 + CSCC-29-T COSM4568699 c.127T>G p.S43A Substitution - Missense 23:143884227-143884227 + YUAKER COSM1715715 c.184G>A p.E62K Substitution - Missense 23:143884284-143884284 + CR108 COSM4994769 c.284A>T p.K95M Substitution - Missense 23:143884384-143884384 + S02360 COSM5696316 c.352C>A p.P118T Substitution - Missense 23:143884452-143884452 + TCGA-EE-A20F-06 COSM3558845 c.7G>A p.E3K Substitution - Missense 23:143884107-143884107 + TCGA-BR-7197-01 COSM4107228 c.317T>C p.L106P Substitution - Missense 23:143884417-143884417 + TCGA-B5-A11N-01 COSM756053 c.381G>A p.V127V Substitution - coding silent 23:143884481-143884481 + TCGA-AX-A063-01 COSM265513 c.307C>T p.R103C Substitution - Missense 23:143884407-143884407 + TCGA-AA-A017-01 COSM287139 c.175C>G p.L59V Substitution - Missense 23:143884275-143884275 + TCGA-EE-A29D-06 COSM3558848 c.232C>T p.H78Y Substitution - Missense 23:143884332-143884332 + TCGA-B4-5844-01 COSM1497241 c.428C>T p.A143V Substitution - Missense 23:143884528-143884528 + TCGA-BR-6452-01 COSM4107223 c.127T>A p.S43T Substitution - Missense 23:143884227-143884227 + CHC892T COSM4794778 c.437G>A p.R146K Substitution - Missense 23:143884537-143884537 + YUBAN COSM1116397 c.323C>T p.S108L Substitution - Missense 23:143884423-143884423 + AOCS-160-1-6 COSM3558845 c.7G>A p.E3K Substitution - Missense 23:143884107-143884107 + ESCC_BICR_061T COSM4107227 c.297C>A p.A99A Substitution - coding silent 23:143884397-143884397 + TCGA-33-4586-01 COSM756055 c.271A>T p.I91F Substitution - Missense 23:143884371-143884371 + TCGA-D1-A15X-01 COSM1116398 c.446C>T p.A149V Substitution - Missense 23:143884546-143884546 + AOCS-124-1-X COSM4137721 c.124G>T p.E42* Substitution - Nonsense 23:143884224-143884224 + TCGA-AA-A010-01 COSM286234 c.313G>A p.V105I Substitution - Missense 23:143884413-143884413 + TCGA-06-0649 COSM267711 c.164G>A p.R55H Substitution - Missense 23:143884264-143884264 + S00830 COSM318254 c.124G>A p.E42K Substitution - Missense 23:143884224-143884224 + PD4107a COSM165368 c.65G>T p.G22V Substitution - Missense 23:143884165-143884165 + YUGAFFE COSM1715717 c.400G>A p.E134K Substitution - Missense 23:143884500-143884500 + TCGA-HU-A4GU-01 COSM4107229 c.380T>C p.V127A Substitution - Missense 23:143884480-143884480 + TCGA-51-4081-01 COSM756053 c.381G>A p.V127V Substitution - coding silent 23:143884481-143884481 + T578 COSM4738691 c.259A>G p.I87V Substitution - Missense 23:143884359-143884359 + TCGA-18-4083-01 COSM756057 c.36C>A p.T12T Substitution - coding silent 23:143884136-143884136 + TCGA-AP-A059-01 COSM1116395 c.61C>A p.P21T Substitution - Missense 23:143884161-143884161 + ESO-K08 COSM1269627 c.88A>C p.S30R Substitution - Missense 23:143884188-143884188 + YURAY COSM5412143 c.298C>T p.L100L Substitution - coding silent 23:143884398-143884398 + PDA_050 COSM5000704 c.266T>G p.L89* Substitution - Nonsense 105T COSM1725210 c.308G>A p.R103H Substitution - Missense 23:143884408-143884408 + 12820 COSM5616237 c.37C>A p.Q13K Substitution - Missense 23:143884137-143884137 + ESCC_BICR_061T COSM5430892 c.341A>G p.N114S Substitution - Missense 23:143884441-143884441 + TCGA-EI-6883-01 COSM3424548 c.341A>T p.N114I Substitution - Missense 23:143884441-143884441 + TCGA-EE-A2MS-06 COSM3558849 c.257G>A p.R86K Substitution - Missense 23:143884357-143884357 + T3024 COSM4738692 c.275T>C p.L92S Substitution - Missense 23:143884375-143884375 + TCGA-D7-5579-01 COSM4107224 c.139C>G p.P47A Substitution - Missense 23:143884239-143884239 + CPCG0201-F1 COSM4879894 c.241G>A p.V81I Substitution - Missense 23:143884341-143884341 + TCGA-AA-3821-01 COSM294927 c.249G>A p.K83K Substitution - coding silent 23:143884349-143884349 + BD177T COSM1242976 c.216C>T p.F72F Substitution - coding silent 23:143884316-143884316 + TCGA-GF-A6C8-06 COSM3913510 c.291C>T p.S97S Substitution - coding silent 23:143884391-143884391 + 55 COSM5013818 c.41G>A p.R14H Substitution - Missense 23:143884141-143884141 + sysucc-1450T COSM5480295 c.163C>T p.R55C Substitution - Missense 23:143884263-143884263 + tumor_4135350 COSM1161806 c.119C>T p.A40V Substitution - Missense 23:143884219-143884219 + TCGA-D1-A16Q-01 COSM1116396 c.145G>A p.E49K Substitution - Missense 23:143884245-143884245 + CN-AML-08-T COSM5000704 c.266T>G p.L89* Substitution - Nonsense YULAN COSM1715716 c.373G>A p.D125N Substitution - Missense 23:143884473-143884473 + C086 COSM1242976 c.216C>T p.F72F Substitution - coding silent 23:143884316-143884316 + ESCC_BICR_061T COSM4107230 c.414T>A p.I138I Substitution - coding silent 23:143884514-143884514 + 202_T COSM3964826 c.324G>T p.S108S Substitution - coding silent 23:143884424-143884424 + TCGA-HU-A4GU-01 COSM4107226 c.262A>T p.S88C Substitution - Missense 23:143884362-143884362 + S01494 COSM316328 c.199G>A p.A67T Substitution - Missense 23:143884299-143884299 + 2217539 COSM4422104 c.66C>A p.G22G Substitution - coding silent 23:143884166-143884166 + TCGA-22-1016-01 COSM756053 c.381G>A p.V127V Substitution - coding silent 23:143884481-143884481 + TCGA-EE-A2MJ-06 COSM3558847 c.106C>T p.H36Y Substitution - Missense 23:143884206-143884206 + ESO-717 COSM1242976 c.216C>T p.F72F Substitution - coding silent 23:143884316-143884316 + TCGA-46-3768-01 COSM756054 c.349A>C p.N117H Substitution - Missense 23:143884449-143884449 + S01170 COSM5667272 c.246C>T p.D82D Substitution - coding silent 23:143884346-143884346 + MedB-1 COSM4107226 c.262A>T p.S88C Substitution - Missense 23:143884362-143884362 + HN_62415 COSM127006 c.283A>T p.K95* Substitution - Nonsense 23:143884383-143884383 + TCGA-B5-A11W-01 COSM1116397 c.323C>T p.S108L Substitution - Missense 23:143884423-143884423 + 587376 COSM1231546 c.410C>A p.A137D Substitution - Missense 23:143884510-143884510 + ESO-147 COSM1116398 c.446C>T p.A149V Substitution - Missense 23:143884546-143884546 + S00830 COSM318254 c.124G>A p.E42K Substitution - Missense 23:143884224-143884224 + TCGA-AG-A032-01 COSM265513 c.307C>T p.R103C Substitution - Missense 23:143884407-143884407 + ESCC_BICR_061T COSM4107229 c.380T>C p.V127A Substitution - Missense 23:143884480-143884480 + CHC1085T COSM4788673 c.343G>A p.A115T Substitution - Missense 23:143884443-143884443 + S01020 COSM5665470 c.296C>A p.A99D Substitution - Missense 23:143884396-143884396 + PD7066a COSM1725210 c.308G>A p.R103H Substitution - Missense 23:143884408-143884408 + CHC892T COSM4794778 c.437G>A p.R146K Substitution - Missense 23:143884537-143884537 + tumor_4177810 COSM5946289 c.277A>C p.K93Q Substitution - Missense 23:143884377-143884377 + CHC1211T COSM4954843 c.94G>T p.A32S Substitution - Missense 23:143884194-143884194 + TCGA-IH-A3EA-01 COSM3558846 c.24C>T p.I8I Substitution - coding silent 23:143884124-143884124 + Pat_46_B COSM4378037 c.362C>T p.P121L Substitution - Missense 23:143884462-143884462 + YUPAER COSM5412144 c.403G>A p.A135T Substitution - Missense 23:143884503-143884503 + TCGA-AD-6895-01 COSM1466154 c.98G>A p.R33H Substitution - Missense 23:143884198-143884198 + TCGA-06-0649 COSM2151468 c.226A>G p.I76V Substitution - Missense 23:143884326-143884326 + TCGA-BF-A3DL-01 COSM1715716 c.373G>A p.D125N Substitution - Missense 23:143884473-143884473 + CHC1085T COSM4788673 c.343G>A p.A115T Substitution - Missense 23:143884443-143884443 + TCGA-D7-6521-01 COSM4107225 c.222C>A p.T74T Substitution - coding silent 23:143884322-143884322 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.585176;Hs.585177 Xq27.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.N117H c.349A>C X 142967551 LUSC A C Missense p.S30R c.88A>C X 142967290 ESCA A C Synonymous p.P79P c.237A>C X 142967439 ESCA A G Missense p.I76V c.226A>G X 142967428 GBM A G Synonymous p.P27P c.81A>G X 142967283 HNSC AG TA Missense p.K95I c.284_285delinsTA X 142967486 GBM AG TC Missense p.V105L c.312_313delinsTC X 142967514 LUAD A T Missense p.I91F c.271A>T X 142967473 LUSC A T Nonsense p.K95* c.283A>T X 142967485 HNSC C A Missense p.N133K c.399C>A X 142967601 HNSC C A Missense p.Q13K c.37C>A X 142967239 NSCLC C A Synonymous p.T12T c.36C>A X 142967238 LUSC C G Missense p.L59V c.175C>G X 142967377 COREAD C G Missense p.P47A c.139C>G X 142967341 STAD C G Missense p.Q110E c.328C>G X 142967530 LUAD C G Missense p.Q129E c.385C>G X 142967587 LUSC C G Missense p.R71G c.211C>G X 142967413 SCLC C T 3-UTRSNV . c.459+42C>T X 142967703 CM C T Missense p.A149V c.446C>T X 142967648 ESCA C T Missense p.A40V c.119C>T X 142967321 DLBCL C T Missense p.H36Y c.106C>T X 142967308 CM C T Missense p.R103C c.307C>T X 142967509 COREAD C T Missense p.R103C c.307C>T X 142967509 UCEC C T Missense p.R33C c.97C>T X 142967299 CM C T Missense p.S108L c.323C>T X 142967525 UCEC C T Synonymous p.A67A c.201C>T X 142967403 CM C T Synonymous p.F72F c.216C>T X 142967418 CM C T Synonymous p.I8I c.24C>T X 142967226 CM C T Synonymous p.N31N c.93C>T X 142967295 GBM G A Missense p.A67T c.199G>A X 142967401 SCLC G A Missense p.D125N c.373G>A X 142967575 CM G A Missense p.E134K c.400G>A X 142967602 CM G A Missense p.E3K c.7G>A X 142967209 CM G A Missense p.E42K c.124G>A X 142967326 CM G A Missense p.E42K c.124G>A X 142967326 SCLC G A Missense p.E49K c.145G>A X 142967347 UCEC G A Missense p.R55H c.164G>A X 142967366 GBM G A Missense p.R86K c.257G>A X 142967459 CM G A Synonymous p.V127V c.381G>A X 142967583 LUSC G T Missense p.G22V c.65G>T X 142967267 BRCA G T Missense p.V38F c.112G>T X 142967314 LUAD G T Synonymous p.V127V c.381G>T X 142967583 LUAD T A Missense p.I39N c.116T>A X 142967318 LUAD T A Synonymous p.A40A c.120T>A X 142967322 HNSC T - Frameshift p.P21Lfs*53 c.60delT X 142967261 STAD