Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand YUKAT COSM5412797 c.1566G>A p.W522* Substitution - Nonsense 23:49881483-49881483 + TCGA-D1-A101-01 COSM1122530 c.1063C>A p.P355T Substitution - Missense 23:49880980-49880980 + TCGA-AP-A0LF-01 COSM1122534 c.1381C>G p.L461V Substitution - Missense 23:49881298-49881298 + PT51 COSM5938546 c.1166G>A p.G389E Substitution - Missense 23:49881083-49881083 + GHE0988 COSM5715059 c.970C>T p.H324Y Substitution - Missense 23:49880887-49880887 + BCM439T COSM4951895 c.1303G>A p.V435I Substitution - Missense 23:49881220-49881220 + TCGA-F5-6814-01 COSM3424842 c.705C>A p.F235L Substitution - Missense 23:49880622-49880622 + I2L-P7-Tumor-Organoid COSM5367467 c.1044C>T p.G348G Substitution - coding silent 23:49880961-49880961 + ESCC-139T COSM1122527 c.854G>A p.R285H Substitution - Missense 23:49880771-49880771 + TCGA-BS-A0UJ-01 COSM1122525 c.624A>C p.R208S Substitution - Missense 23:49880541-49880541 + TCGA-DM-A0XD-01 COSM1468372 c.611C>T p.T204M Substitution - Missense 23:49880528-49880528 + 426 COSM4432973 c.736C>T p.P246S Substitution - Missense 23:49880653-49880653 + ACINAR28 COSM1734754 c.583A>G p.R195G Substitution - Missense 23:49880500-49880500 + C32 COSM4619359 c.1342A>C p.K448Q Substitution - Missense 23:49881259-49881259 + BCM439T COSM4951895 c.1303G>A p.V435I Substitution - Missense 23:49881220-49881220 + TCGA-AD-6889-01 COSM1468375 c.1288A>G p.N430D Substitution - Missense 23:49881205-49881205 + ESCC_44 COSM5630218 c.613A>C p.I205L Substitution - Missense 23:49880530-49880530 + TCGA-D1-A17M-01 COSM1122528 c.855C>T p.R285R Substitution - coding silent 23:49880772-49880772 + PTC-10C COSM4156896 c.808C>A p.P270T Substitution - Missense 23:49880725-49880725 + HCC39T COSM1625961 c.804G>A p.P268P Substitution - coding silent 23:49880721-49880721 + TCGA-D1-A177-01 COSM1122522 c.381A>G p.I127M Substitution - Missense 23:49880298-49880298 + TCGA-AP-A059-01 COSM1122533 c.1374C>A p.S458S Substitution - coding silent 23:49881291-49881291 + TCGA-AP-A059-01 COSM1122527 c.854G>A p.R285H Substitution - Missense 23:49880771-49880771 + PT27 COSM5906250 c.1462G>A p.G488R Substitution - Missense 23:49881379-49881379 + TCGA-A5-A0VP-01 COSM1122532 c.1341G>A p.A447A Substitution - coding silent 23:49881258-49881258 + Au4 COSM5605305 c.1132G>A p.E378K Substitution - Missense 23:49881049-49881049 + TCGA-BG-A0M4-01 COSM1122523 c.411T>C p.Y137Y Substitution - coding silent 23:49880328-49880328 + TCGA-D1-A174-01 COSM1122526 c.646A>G p.T216A Substitution - Missense 23:49880563-49880563 + PD4959a COSM4776028 c.612G>A p.T204T Substitution - coding silent 23:49880529-49880529 + TCGA-BG-A0VV-01 COSM1122535 c.1611C>T p.D537D Substitution - coding silent 23:49881528-49881528 + OSCC-GB_00740111 COSM4890989 c.1482T>A p.Y494* Substitution - Nonsense 23:49881399-49881399 + S00501 COSM5658638 c.679A>G p.T227A Substitution - Missense 23:49880596-49880596 + TCGA-B5-A0JY-01 COSM1122524 c.439G>T p.E147* Substitution - Nonsense 23:49880356-49880356 + ESCC-015T COSM3940024 c.1202C>T p.T401M Substitution - Missense 23:49881119-49881119 + SNU-175 COSM4650887 c.1401G>A p.P467P Substitution - coding silent 23:49881318-49881318 + SJHYPO125 COSM4776028 c.612G>A p.T204T Substitution - coding silent 23:49880529-49880529 + BD14T COSM5517262 c.330C>T p.H110H Substitution - coding silent 23:49880247-49880247 + TCGA-BG-A0M8-01 COSM1122531 c.1340C>T p.A447V Substitution - Missense 23:49881257-49881257 + TCGA-AP-A054-01 COSM1122529 c.973T>C p.C325R Substitution - Missense 23:49880890-49880890 + Gp5D COSM4629032 c.1550A>G p.H517R Substitution - Missense 23:49881467-49881467 + HCC38 COSM1625962 c.1257C>T p.S419S Substitution - coding silent 23:49881174-49881174 + TCGA-D1-A17Q-01 COSM1122532 c.1341G>A p.A447A Substitution - coding silent 23:49881258-49881258 + MO_1012 COSM5556572 c.1646A>T p.H549L Substitution - Missense 23:49881563-49881563 + HCC38T COSM1625962 c.1257C>T p.S419S Substitution - coding silent 23:49881174-49881174 + EGC15 COSM5064734 c.1302C>T p.V434V Substitution - coding silent 23:49881219-49881219 + CSCC-16-T COSM4514706 c.1374C>T p.S458S Substitution - coding silent 23:49881291-49881291 + Gp2D COSM4629032 c.1550A>G p.H517R Substitution - Missense 23:49881467-49881467 + HCC39 COSM1625961 c.804G>A p.P268P Substitution - coding silent 23:49880721-49880721 + 61 COSM5742283 c.1193G>A p.R398Q Substitution - Missense 23:49881110-49881110 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.143562;Hs.143587 Xp11.23