Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand UD-SCC-2 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + TCGA-ES-A2HS-01 COSM4910641 c.4623C>T p.A1541A Substitution - coding silent 22:21388481-21388481 + WSU-HN13 COSM4135208 c.4672G>A p.V1558M Substitution - Missense 22:21388530-21388530 + SCC-25 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + CN-AML-CR-13-Dx COSM5426439 c.1194C>T p.N398N Substitution - coding silent 22:21385052-21385052 + WSU-HN8 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + UM-SCC-11B COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + STC291 COSM5057700 c.4588C>T p.R1530C Substitution - Missense 22:21388446-21388446 + NOKSI COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + CHC433T COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + PTC-50C COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + PTC-46C COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + WSU-HN13 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + PTC-1C COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + SCC-15 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + WSU-HN6 COSM4135208 c.4672G>A p.V1558M Substitution - Missense 22:21388530-21388530 + UPCI:SCC090 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + PTC-73C COSM4135208 c.4672G>A p.V1558M Substitution - Missense 22:21388530-21388530 + WSU-HN12 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + BHY COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + UM-SCC-4 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + CAL27 COSM4592975 c.3184T>C p.W1062R Substitution - Missense 22:21387042-21387042 + WSU-HN12 COSM4601281 c.4661G>T p.G1554V Substitution - Missense 22:21388519-21388519 + WSU-HN13 COSM3308798 c.4534G>A p.G1512R Substitution - Missense 22:21388392-21388392 + WSU-HN30 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + UM-SCC-17B COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + ORL-48 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + WSU-HN6 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + UM-SCC-17B COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + 93VU147T COSM4135208 c.4672G>A p.V1558M Substitution - Missense 22:21388530-21388530 + CAL27 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + NOKSI COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + CAL33 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + UM-SCC-4 COSM4135208 c.4672G>A p.V1558M Substitution - Missense 22:21388530-21388530 + WSU-HN13 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + TCGA-76-4927-01 COSM3405533 c.4595C>G p.P1532R Substitution - Missense 22:21388453-21388453 + Detroit_562 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + TCGA-BP-4174-01 COSM3774004 c.4242G>C p.V1414V Substitution - coding silent 22:21388100-21388100 + SCC-9 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + CN-AML-CR-42-Dx COSM5428236 c.3817A>G p.S1273G Substitution - Missense 22:21387675-21387675 + UM-SCC-2 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + Detroit_562 COSM3774004 c.4242G>C p.V1414V Substitution - coding silent 22:21388100-21388100 + BHY COSM4592975 c.3184T>C p.W1062R Substitution - Missense 22:21387042-21387042 + 347 COSM3724434 c.1956_1957insCC p.S653fs*4 Insertion - Frameshift 22:21385814-21385815 + UM-SCC-2 COSM4599521 c.3439G>C p.V1147L Substitution - Missense 22:21387297-21387297 + CAL27 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + 93VU147T COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + UM-SCC-47 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + WSU-HN30 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + WSU-HN6 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + BHY COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + UM-SCC-11B COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + BICR_22 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + TCGA-AD-5900-01 COSM1415059 c.4761delG p.G1589fs*9 Deletion - Frameshift 22:21388619-21388619 + SCC-9 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + 587332 COSM1223745 c.3283G>A p.E1095K Substitution - Missense 22:21387141-21387141 + SCC-25 COSM4135208 c.4672G>A p.V1558M Substitution - Missense 22:21388530-21388530 + UD-SCC-2 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + TCGA-G4-6293-01 COSM1415058 c.1957_1958insCC p.G654fs*3 Insertion - Frameshift 22:21385815-21385816 + SCC-15 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + B73-Tumor COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + 93VU147T COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + PDA_060 COSM1415058 c.1957_1958insCC p.G654fs*3 Insertion - Frameshift 22:21385815-21385816 + CN-AML-CR-30-Dx COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + CN-AML-CR-5-Dx COSM3774004 c.4242G>C p.V1414V Substitution - coding silent 22:21388100-21388100 + UPCI:SCC090 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + SNUH_G57_S1 COSM3681390 c.1477T>G p.C493G Substitution - Missense 22:21385335-21385335 + CN-AML-CR-42-Dx COSM5428235 c.3788A>C p.E1263A Substitution - Missense 22:21387646-21387646 + UM-SCC-2 COSM4599631 c.3161T>C p.V1054A Substitution - Missense 22:21387019-21387019 + TCGA-EE-A2GI-06 COSM3552396 c.3234C>T p.F1078F Substitution - coding silent 22:21387092-21387092 + SNUH_G28_S1 COSM3681389 c.583G>A p.E195K Substitution - Missense 22:21384441-21384441 + TCGA-AF-6672-01 COSM1415058 c.1957_1958insCC p.G654fs*3 Insertion - Frameshift 22:21385815-21385816 + TCGA-A2-A0T5-01 COSM3842250 c.4625A>C p.H1542P Substitution - Missense 22:21388483-21388483 + TCGA-AB-2832-03 COSM1318786 c.2760G>A p.A920A Substitution - coding silent 22:21386618-21386618 + CN-AML-CR-54-Dx COSM3681389 c.583G>A p.E195K Substitution - Missense 22:21384441-21384441 + CAL33 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + SCC-25 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + CN-AML-CR-16-Dx COSM5427974 c.3919C>A p.P1307T Substitution - Missense 22:21387777-21387777 + ORL-48 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + UM-SCC-47 COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 + 1517_PT COSM5755711 c.4580G>T p.R1527M Substitution - Missense 22:21388438-21388438 + WSU-HN12 COSM4135207 c.4537C>T p.R1513C Substitution - Missense 22:21388395-21388395 + CN-AML-CR-21-Dx COSM1484095 c.4451G>A p.R1484K Substitution - Missense 22:21388309-21388309 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.568257 22q11.21 612700

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - C Frameshift p.T1495Hfs*3 c.4482dupC 22 21742629 GBM C G Missense p.P1532R c.4595C>G 22 21742742 GBM C T Synonymous p.F1078F c.3234C>T 22 21741381 CM G A Missense p.G1535E c.4604G>A 22 21742751 CM G C Missense p.E1544Q c.4630G>C 22 21742777 LUAD