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 11 67206163 67206163 + Silent SNP G G A TCGA-OR-A5J4-01A-11D-A29I-10 TCGA-OR-A5J4-10A-01D-A29L-10 g.chr11:67206163G>A c.1323C>T c.(1321-1323)agC>agT p.S441S BLCA 11 67205880 67205880 + Silent SNP C C T TCGA-FD-A43N-01A-11D-A23U-08 TCGA-FD-A43N-10A-01D-A23U-08 g.chr11:67205880C>T c.1437G>A c.(1435-1437)gaG>gaA p.E479E BLCA 11 67207599 67207599 + Missense_Mutation SNP C C G TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr11:67207599C>G c.997G>C c.(997-999)Gag>Cag p.E333Q BLCA 11 67207901 67207901 + Missense_Mutation SNP C C G TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr11:67207901C>G c.766G>C c.(766-768)Gag>Cag p.E256Q BLCA 11 67208697 67208697 + Nonsense_Mutation SNP C C A TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr11:67208697C>A c.655G>T c.(655-657)Gag>Tag p.E219* BLCA 11 67209533 67209533 + Silent SNP C C T TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr11:67209533C>T c.228G>A c.(226-228)ccG>ccA p.P76P BRCA 11 67207618 67207619 + Frame_Shift_Ins INS - - C TCGA-B6-A0IN-01A-11W-A050-09 TCGA-B6-A0IN-10A-01W-A055-09 g.chr11:67207618_67207619insC c.977_978insG c.(976-978)ggcfs p.G326fs BRCA 11 67209552 67209552 + Missense_Mutation SNP C C T TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr11:67209552C>T c.209G>A c.(208-210)cGc>cAc p.R70H CESC 11 67207593 67207593 + Missense_Mutation SNP C C T TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr11:67207593C>T c.1003G>A c.(1003-1005)Gcc>Acc p.A335T CESC 11 67208821 67208821 + Missense_Mutation SNP G G A TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr11:67208821G>A c.619C>T c.(619-621)Cgg>Tgg p.R207W COAD 11 67206254 67206254 + Missense_Mutation SNP A A G TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr11:67206254A>G c.1232T>C c.(1231-1233)gTg>gCg p.V411A COAD 11 67207812 67207812 + Silent SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:67207812G>A c.855C>T c.(853-855)tgC>tgT p.C285C COAD 11 67208981 67208981 + Silent SNP G G A TCGA-AD-6899-01A-11D-1924-10 TCGA-AD-6899-10A-01D-1924-10 g.chr11:67208981G>A c.459C>T c.(457-459)tgC>tgT p.C153C COAD 11 67209475 67209475 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:67209475C>T c.286G>A c.(286-288)Gaa>Aaa p.E96K COADREAD 11 67206254 67206254 + Missense_Mutation SNP A A G TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr11:67206254A>G c.1232T>C c.(1231-1233)gTg>gCg p.V411A COADREAD 11 67207812 67207812 + Silent SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:67207812G>A c.855C>T c.(853-855)tgC>tgT p.C285C COADREAD 11 67208981 67208981 + Silent SNP G G A TCGA-AD-6899-01A-11D-1924-10 TCGA-AD-6899-10A-01D-1924-10 g.chr11:67208981G>A c.459C>T c.(457-459)tgC>tgT p.C153C COADREAD 11 67209475 67209475 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:67209475C>T c.286G>A c.(286-288)Gaa>Aaa p.E96K ESCA 11 67207669 67207669 + Silent SNP C C T TCGA-V5-A7RB-01A-11D-A351-09 TCGA-V5-A7RB-10A-01D-A351-09 g.chr11:67207669C>T c.927G>A c.(925-927)acG>acA p.T309T ESCA 11 67210002 67210002 + Missense_Mutation SNP C C T TCGA-JY-A93E-01A-11D-A37C-09 TCGA-JY-A93E-10A-01D-A37F-09 g.chr11:67210002C>T c.98G>A c.(97-99)cGt>cAt p.R33H HNSC 11 67206199 67206199 + Silent SNP G G T TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr11:67206199G>T c.1287C>A c.(1285-1287)ccC>ccA p.P429P HNSC 11 67206256 67206256 + Silent SNP G G A TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr11:67206256G>A c.1230C>T c.(1228-1230)aaC>aaT p.N410N HNSC 11 67207899 67207899 + Silent SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr11:67207899C>T c.768G>A c.(766-768)gaG>gaA p.E256E HNSC 11 67208934 67208934 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:67208934T>C c.506A>G c.(505-507)tAc>tGc p.Y169C KIPAN 11 67207603 67207603 + Frame_Shift_Del DEL C C - TCGA-B3-4104-01A-01D-1458-08 TCGA-B3-4104-10A-01D-1458-08 g.chr11:67207603delC c.993delG c.(991-993)aagfs p.K331fs KIPAN 11 67207622 67207622 + Missense_Mutation SNP C C T TCGA-CZ-5455-01A-01D-1501-10 TCGA-CZ-5455-11A-01D-1501-10 g.chr11:67207622C>T c.974G>A c.(973-975)cGg>cAg p.R325Q KIPAN 11 67207642 67207642 + Silent SNP A A G TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr11:67207642A>G c.954T>C c.(952-954)ggT>ggC p.G318G KIRC 11 67207622 67207622 + Missense_Mutation SNP C C T TCGA-CZ-5455-01A-01D-1501-10 TCGA-CZ-5455-11A-01D-1501-10 g.chr11:67207622C>T c.974G>A c.(973-975)cGg>cAg p.R325Q KIRC 11 67207642 67207642 + Silent SNP A A G TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr11:67207642A>G c.954T>C c.(952-954)ggT>ggC p.G318G KIRP 11 67207603 67207603 + Frame_Shift_Del DEL C C - TCGA-B3-4104-01A-01D-1458-08 TCGA-B3-4104-10A-01D-1458-08 g.chr11:67207603delC c.993delG c.(991-993)aagfs p.K331fs LIHC 11 67209971 67209971 + Silent SNP G G C TCGA-XR-A8TC-01A-11D-A35Z-10 TCGA-XR-A8TC-10A-01D-A35Z-10 g.chr11:67209971G>C c.129C>G c.(127-129)gtC>gtG p.V43V LIHC 11 67210003 67210003 + Missense_Mutation SNP G G T TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr11:67210003G>T c.97C>A c.(97-99)Cgt>Agt p.R33S LUAD 11 67208691 67208691 + Missense_Mutation SNP C C A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr11:67208691C>A c.661G>T c.(661-663)Gcc>Tcc p.A221S LUAD 11 67209219 67209219 + Missense_Mutation SNP C C T TCGA-05-5428-01A-01D-1625-08 TCGA-05-5428-10A-01D-1625-08 g.chr11:67209219C>T c.439G>A c.(439-441)Gtg>Atg p.V147M LUAD 11 67209532 67209532 + Missense_Mutation SNP T T A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr11:67209532T>A c.229A>T c.(229-231)Acg>Tcg p.T77S LUSC 11 67207901 67207901 + Missense_Mutation SNP C C G TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr11:67207901C>G c.766G>C c.(766-768)Gag>Cag p.E256Q OV 11 67210003 67210003 + Missense_Mutation SNP G G A TCGA-25-1319-01A-01W-0492-08 TCGA-25-1319-10A-01W-0492-08 g.chr11:67210003G>A c.97C>T c.(97-99)Cgt>Tgt p.R33C PAAD 11 67205955 67205955 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:67205955C>A c.1362G>T c.(1360-1362)gaG>gaT p.E454D PAAD 11 67206391 67206391 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:67206391G>A c.1095C>T c.(1093-1095)ccC>ccT p.P365P PAAD 11 67209273 67209273 + Missense_Mutation SNP C C G TCGA-HZ-A8P1-01A-11D-A377-08 TCGA-HZ-A8P1-10A-01D-A37A-08 g.chr11:67209273C>G c.385G>C c.(385-387)Gag>Cag p.E129Q PRAD 11 67205932 67205932 + Missense_Mutation SNP G G T TCGA-EJ-7785-01A-11D-2114-08 TCGA-EJ-7785-10A-01D-2114-08 g.chr11:67205932G>T c.1385C>A c.(1384-1386)gCc>gAc p.A462D PRAD 11 67206326 67206326 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:67206326G>A c.1160C>T c.(1159-1161)cCg>cTg p.P387L SKCM 11 67205905 67205905 + Missense_Mutation SNP C C A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:67205905C>A c.1412G>T c.(1411-1413)gGc>gTc p.G471V SKCM 11 67205906 67205906 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:67205906C>T c.1411G>A c.(1411-1413)Ggc>Agc p.G471S SKCM 11 67207678 67207678 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:67207678G>A c.918C>T c.(916-918)ttC>ttT p.F306F SKCM 11 67208889 67208889 + Missense_Mutation SNP C C A TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr11:67208889C>A c.551G>T c.(550-552)tGg>tTg p.W184L SKCM 11 67210079 67210079 + Silent SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:67210079G>A c.21C>T c.(19-21)gtC>gtT p.V7V

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 11 67201886 67201886 single base substitution C T downstream_gene_variant BLCA-US 11 67207901 67207901 single base substitution C G 3_prime_UTR_variant BLCA-US 11 67207901 67207901 single base substitution C G downstream_gene_variant BLCA-US 11 67207901 67207901 single base substitution C G exon_variant BLCA-US 11 67207901 67207901 single base substitution C G missense_variant E256Q 766G>C BLCA-US 11 67207901 67207901 single base substitution C G upstream_gene_variant BRCA-EU 11 67200537 67200537 single base substitution G A downstream_gene_variant BRCA-EU 11 67200911 67200911 single base substitution T G downstream_gene_variant BRCA-EU 11 67201227 67201227 single base substitution T A downstream_gene_variant BRCA-EU 11 67201728 67201728 single base substitution C T downstream_gene_variant BRCA-EU 11 67202025 67202025 single base substitution G T downstream_gene_variant BRCA-EU 11 67202392 67202392 single base substitution C G downstream_gene_variant BRCA-EU 11 67202520 67202520 single base substitution G A downstream_gene_variant BRCA-EU 11 67203835 67203835 single base substitution G A downstream_gene_variant BRCA-EU 11 67203969 67203969 single base substitution G A downstream_gene_variant BRCA-EU 11 67204360 67204360 single base substitution C G downstream_gene_variant BRCA-EU 11 67204953 67204953 single base substitution C G downstream_gene_variant BRCA-EU 11 67205280 67205280 single base substitution G T downstream_gene_variant BRCA-EU 11 67205885 67205885 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 67205885 67205885 single base substitution C G downstream_gene_variant BRCA-EU 11 67205885 67205885 single base substitution C G exon_variant BRCA-EU 11 67205885 67205885 single base substitution C G missense_variant E478Q 1432G>C BRCA-EU 11 67206440 67206440 single base substitution G C downstream_gene_variant BRCA-EU 11 67206440 67206440 single base substitution G C intron_variant BRCA-EU 11 67207614 67207614 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 67207614 67207614 single base substitution C G downstream_gene_variant BRCA-EU 11 67207614 67207614 single base substitution C G missense_variant E328Q 982G>C BRCA-EU 11 67207614 67207614 single base substitution C G splice_region_variant BRCA-EU 11 67209030 67209030 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 67209030 67209030 single base substitution G A downstream_gene_variant BRCA-EU 11 67209030 67209030 single base substitution G A intron_variant BRCA-EU 11 67209030 67209030 single base substitution G A upstream_gene_variant BRCA-EU 11 67209651 67209651 single base substitution C A intron_variant BRCA-EU 11 67209651 67209651 single base substitution C A upstream_gene_variant BRCA-EU 11 67212089 67212089 single base substitution C T upstream_gene_variant BRCA-EU 11 67212131 67212131 single base substitution G A upstream_gene_variant BRCA-EU 11 67214004 67214004 single base substitution G T upstream_gene_variant BRCA-EU 11 67214044 67214044 single base substitution T C upstream_gene_variant BRCA-EU 11 67214667 67214667 single base substitution G C upstream_gene_variant BRCA-EU 11 67214794 67214794 single base substitution A T upstream_gene_variant BRCA-EU 11 67215199 67215199 single base substitution C T upstream_gene_variant BRCA-FR 11 67201688 67201688 single base substitution A C downstream_gene_variant BRCA-FR 11 67203123 67203123 single base substitution C T downstream_gene_variant BRCA-FR 11 67204360 67204360 single base substitution C G downstream_gene_variant BRCA-FR 11 67204953 67204953 single base substitution C G downstream_gene_variant BRCA-KR 11 67209178 67209178 single base substitution A G downstream_gene_variant BRCA-KR 11 67209178 67209178 single base substitution A G intron_variant BRCA-KR 11 67209178 67209178 single base substitution A G synonymous_variant A160A 480T>C BRCA-KR 11 67209178 67209178 single base substitution A G upstream_gene_variant BRCA-UK 11 67205885 67205885 single base substitution C G 3_prime_UTR_variant BRCA-UK 11 67205885 67205885 single base substitution C G downstream_gene_variant BRCA-UK 11 67205885 67205885 single base substitution C G exon_variant BRCA-UK 11 67205885 67205885 single base substitution C G missense_variant E478Q 1432G>C BRCA-US 11 67200852 67200852 single base substitution G C downstream_gene_variant BRCA-US 11 67200889 67200889 single base substitution A C downstream_gene_variant BRCA-US 11 67200919 67200919 single base substitution G T downstream_gene_variant BRCA-US 11 67202530 67202530 single base substitution C G downstream_gene_variant BRCA-US 11 67203502 67203502 deletion of <=200bp T - downstream_gene_variant BRCA-US 11 67206199 67206199 deletion of <=200bp G - 3_prime_UTR_variant BRCA-US 11 67206199 67206199 deletion of <=200bp G - downstream_gene_variant BRCA-US 11 67206199 67206199 deletion of <=200bp G - exon_variant BRCA-US 11 67206199 67206199 deletion of <=200bp G - frameshift_variant P429 BRCA-US 11 67207618 67207618 insertion of <=200bp - C 3_prime_UTR_variant BRCA-US 11 67207618 67207618 insertion of <=200bp - C downstream_gene_variant BRCA-US 11 67207618 67207618 insertion of <=200bp - C exon_variant BRCA-US 11 67207618 67207618 insertion of <=200bp - C frameshift_variant G326G? BRCA-US 11 67209552 67209552 single base substitution C T exon_variant BRCA-US 11 67209552 67209552 single base substitution C T missense_variant R70H 209G>A BRCA-US 11 67209552 67209552 single base substitution C T upstream_gene_variant BTCA-JP 11 67200627 67200627 single base substitution C T downstream_gene_variant BTCA-JP 11 67201008 67201008 single base substitution C T downstream_gene_variant BTCA-JP 11 67201819 67201819 single base substitution G A downstream_gene_variant BTCA-JP 11 67201928 67201928 single base substitution C G downstream_gene_variant BTCA-JP 11 67205978 67205978 single base substitution G A downstream_gene_variant BTCA-JP 11 67205978 67205978 single base substitution G A intron_variant BTCA-JP 11 67209168 67209168 deletion of <=200bp G - downstream_gene_variant BTCA-JP 11 67209168 67209168 deletion of <=200bp G - frameshift_variant H164 BTCA-JP 11 67209168 67209168 deletion of <=200bp G - intron_variant BTCA-JP 11 67209168 67209168 deletion of <=200bp G - upstream_gene_variant BTCA-JP 11 67209869 67209869 single base substitution T G intron_variant BTCA-JP 11 67209869 67209869 single base substitution T G upstream_gene_variant CESC-US 11 67200648 67200648 single base substitution G A downstream_gene_variant CESC-US 11 67200801 67200801 single base substitution C A downstream_gene_variant CESC-US 11 67202296 67202296 single base substitution C T downstream_gene_variant CESC-US 11 67202364 67202364 single base substitution C A downstream_gene_variant CESC-US 11 67207593 67207593 single base substitution C T 3_prime_UTR_variant CESC-US 11 67207593 67207593 single base substitution C T downstream_gene_variant CESC-US 11 67207593 67207593 single base substitution C T intron_variant CESC-US 11 67207593 67207593 single base substitution C T missense_variant A335T 1003G>A CESC-US 11 67208821 67208821 single base substitution G A 3_prime_UTR_variant CESC-US 11 67208821 67208821 single base substitution G A downstream_gene_variant CESC-US 11 67208821 67208821 single base substitution G A exon_variant CESC-US 11 67208821 67208821 single base substitution G A missense_variant R207W 619C>T CESC-US 11 67208821 67208821 single base substitution G A upstream_gene_variant CLLE-ES 11 67201866 67201866 single base substitution A G downstream_gene_variant CLLE-ES 11 67204602 67204602 single base substitution G A downstream_gene_variant COAD-US 11 67200819 67200819 single base substitution C T downstream_gene_variant COAD-US 11 67201897 67201897 single base substitution C T downstream_gene_variant COAD-US 11 67202156 67202156 single base substitution C T downstream_gene_variant COAD-US 11 67203565 67203565 deletion of <=200bp G - downstream_gene_variant COAD-US 11 67203608 67203608 single base substitution C T downstream_gene_variant COAD-US 11 67207812 67207812 single base substitution G A 3_prime_UTR_variant COAD-US 11 67207812 67207812 single base substitution G A downstream_gene_variant COAD-US 11 67207812 67207812 single base substitution G A exon_variant COAD-US 11 67207812 67207812 single base substitution G A synonymous_variant C285C 855C>T COAD-US 11 67207812 67207812 single base substitution G A upstream_gene_variant COAD-US 11 67208963 67208963 single base substitution G A 3_prime_UTR_variant COAD-US 11 67208963 67208963 single base substitution G A downstream_gene_variant COAD-US 11 67208963 67208963 single base substitution G A exon_variant COAD-US 11 67208963 67208963 single base substitution G A synonymous_variant I159I 477C>T COAD-US 11 67208963 67208963 single base substitution G A upstream_gene_variant COAD-US 11 67208981 67208981 single base substitution G A 3_prime_UTR_variant COAD-US 11 67208981 67208981 single base substitution G A downstream_gene_variant COAD-US 11 67208981 67208981 single base substitution G A exon_variant COAD-US 11 67208981 67208981 single base substitution G A synonymous_variant C153C 459C>T COAD-US 11 67208981 67208981 single base substitution G A upstream_gene_variant COAD-US 11 67209475 67209475 single base substitution C T exon_variant COAD-US 11 67209475 67209475 single base substitution C T missense_variant E96K 286G>A COAD-US 11 67209475 67209475 single base substitution C T upstream_gene_variant COAD-US 11 67209530 67209530 single base substitution C T exon_variant COAD-US 11 67209530 67209530 single base substitution C T synonymous_variant T77T 231G>A COAD-US 11 67209530 67209530 single base substitution C T upstream_gene_variant COCA-CN 11 67200837 67200837 single base substitution G T downstream_gene_variant COCA-CN 11 67201782 67201782 single base substitution G C downstream_gene_variant COCA-CN 11 67201850 67201850 single base substitution G A downstream_gene_variant COCA-CN 11 67205079 67205079 single base substitution G A downstream_gene_variant COCA-CN 11 67209869 67209869 single base substitution T G intron_variant COCA-CN 11 67209869 67209869 single base substitution T G upstream_gene_variant EOPC-DE 11 67201241 67201241 single base substitution C T downstream_gene_variant ESAD-UK 11 67200637 67200637 single base substitution G A downstream_gene_variant ESAD-UK 11 67201244 67201244 single base substitution G A downstream_gene_variant ESAD-UK 11 67202470 67202470 single base substitution T G downstream_gene_variant ESAD-UK 11 67204204 67204207 deletion of <=200bp ATGT - downstream_gene_variant ESAD-UK 11 67204209 67204211 deletion of <=200bp TAT - downstream_gene_variant ESAD-UK 11 67204835 67204835 single base substitution G A downstream_gene_variant ESAD-UK 11 67209169 67209169 single base substitution G T downstream_gene_variant ESAD-UK 11 67209169 67209169 single base substitution G T intron_variant ESAD-UK 11 67209169 67209169 single base substitution G T synonymous_variant P163P 489C>A ESAD-UK 11 67209169 67209169 single base substitution G T upstream_gene_variant ESAD-UK 11 67210212 67210212 single base substitution C G intron_variant ESAD-UK 11 67210212 67210212 single base substitution C G upstream_gene_variant ESAD-UK 11 67212785 67212785 single base substitution C G upstream_gene_variant ESAD-UK 11 67215342 67215342 insertion of <=200bp - G upstream_gene_variant KIRC-US 11 67203476 67203476 single base substitution G T downstream_gene_variant KIRC-US 11 67207622 67207622 single base substitution C T 3_prime_UTR_variant KIRC-US 11 67207622 67207622 single base substitution C T downstream_gene_variant KIRC-US 11 67207622 67207622 single base substitution C T exon_variant KIRC-US 11 67207622 67207622 single base substitution C T missense_variant R325Q 974G>A KIRP-US 11 67203274 67203287 deletion of <=200bp GCAAAGGCGTGCAG - downstream_gene_variant LAML-KR 11 67202044 67202044 single base substitution G A downstream_gene_variant LAML-KR 11 67205978 67205978 single base substitution G A downstream_gene_variant LAML-KR 11 67205978 67205978 single base substitution G A intron_variant LGG-US 11 67203469 67203469 single base substitution G A downstream_gene_variant LICA-CN 11 67200628 67200628 single base substitution A T downstream_gene_variant LIHC-US 11 67200629 67200629 single base substitution A G downstream_gene_variant LIHC-US 11 67210047 67210047 single base substitution T C exon_variant LIHC-US 11 67210047 67210047 single base substitution T C missense_variant Q18R 53A>G LIHC-US 11 67210047 67210047 single base substitution T C upstream_gene_variant LINC-JP 11 67200793 67200793 single base substitution A G downstream_gene_variant LINC-JP 11 67201070 67201070 single base substitution A T downstream_gene_variant LINC-JP 11 67203392 67203392 single base substitution C T downstream_gene_variant LINC-JP 11 67206021 67206021 single base substitution A C downstream_gene_variant LINC-JP 11 67206021 67206021 single base substitution A C intron_variant LINC-JP 11 67207495 67207495 single base substitution T C downstream_gene_variant LINC-JP 11 67207495 67207495 single base substitution T C intron_variant LINC-JP 11 67207507 67207507 single base substitution T C downstream_gene_variant LINC-JP 11 67207507 67207507 single base substitution T C intron_variant LINC-JP 11 67212190 67212190 single base substitution G T upstream_gene_variant LIRI-JP 11 67206391 67206391 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 67206391 67206391 single base substitution G A downstream_gene_variant LIRI-JP 11 67206391 67206391 single base substitution G A exon_variant LIRI-JP 11 67206391 67206391 single base substitution G A synonymous_variant P365P 1095C>T LIRI-JP 11 67209100 67209100 single base substitution A C 3_prime_UTR_variant LIRI-JP 11 67209100 67209100 single base substitution A C downstream_gene_variant LIRI-JP 11 67209100 67209100 single base substitution A C intron_variant LIRI-JP 11 67209100 67209100 single base substitution A C upstream_gene_variant LIRI-JP 11 67215403 67215403 single base substitution C T upstream_gene_variant LIRI-JP 11 67216048 67216048 single base substitution G A upstream_gene_variant LUSC-KR 11 67200812 67200812 single base substitution C T downstream_gene_variant LUSC-KR 11 67202184 67202184 single base substitution G C downstream_gene_variant LUSC-KR 11 67208821 67208821 single base substitution G T 3_prime_UTR_variant LUSC-KR 11 67208821 67208821 single base substitution G T downstream_gene_variant LUSC-KR 11 67208821 67208821 single base substitution G T exon_variant LUSC-KR 11 67208821 67208821 single base substitution G T synonymous_variant R207R 619C>A LUSC-KR 11 67208821 67208821 single base substitution G T upstream_gene_variant LUSC-KR 11 67208831 67208831 single base substitution G A 3_prime_UTR_variant LUSC-KR 11 67208831 67208831 single base substitution G A downstream_gene_variant LUSC-KR 11 67208831 67208831 single base substitution G A exon_variant LUSC-KR 11 67208831 67208831 single base substitution G A synonymous_variant I203I 609C>T LUSC-KR 11 67208831 67208831 single base substitution G A upstream_gene_variant LUSC-KR 11 67210134 67210134 single base substitution C G intron_variant LUSC-KR 11 67210134 67210134 single base substitution C G upstream_gene_variant LUSC-KR 11 67211796 67211796 single base substitution G T upstream_gene_variant LUSC-US 11 67201893 67201893 single base substitution C T downstream_gene_variant LUSC-US 11 67202553 67202553 single base substitution G T downstream_gene_variant LUSC-US 11 67203563 67203563 single base substitution C T downstream_gene_variant LUSC-US 11 67207901 67207901 single base substitution C G 3_prime_UTR_variant LUSC-US 11 67207901 67207901 single base substitution C G downstream_gene_variant LUSC-US 11 67207901 67207901 single base substitution C G exon_variant LUSC-US 11 67207901 67207901 single base substitution C G missense_variant E256Q 766G>C LUSC-US 11 67207901 67207901 single base substitution C G upstream_gene_variant MALY-DE 11 67200543 67200543 single base substitution G T downstream_gene_variant MALY-DE 11 67201458 67201458 single base substitution T C downstream_gene_variant MALY-DE 11 67202107 67202107 single base substitution T C downstream_gene_variant MALY-DE 11 67205961 67205961 single base substitution C T 3_prime_UTR_variant MALY-DE 11 67205961 67205961 single base substitution C T downstream_gene_variant MALY-DE 11 67205961 67205961 single base substitution C T exon_variant MALY-DE 11 67205961 67205961 single base substitution C T synonymous_variant K452K 1356G>A MALY-DE 11 67206827 67206827 single base substitution A C downstream_gene_variant MALY-DE 11 67206827 67206827 single base substitution A C intron_variant MALY-DE 11 67213310 67213310 single base substitution T G upstream_gene_variant MALY-DE 11 67213503 67213503 single base substitution A G upstream_gene_variant MALY-DE 11 67213984 67213984 single base substitution A G upstream_gene_variant MALY-DE 11 67214755 67214775 deletion of <=200bp GTGAGCTGAGATCACGCCATT - upstream_gene_variant MALY-DE 11 67215758 67215758 single base substitution A C upstream_gene_variant MALY-DE 11 67216144 67216144 single base substitution A G upstream_gene_variant MELA-AU 11 67200659 67200659 single base substitution C T downstream_gene_variant MELA-AU 11 67200812 67200812 single base substitution C T downstream_gene_variant MELA-AU 11 67201006 67201006 single base substitution C T downstream_gene_variant MELA-AU 11 67201303 67201303 single base substitution C T downstream_gene_variant MELA-AU 11 67202592 67202592 single base substitution C T downstream_gene_variant MELA-AU 11 67202652 67202652 single base substitution G A downstream_gene_variant MELA-AU 11 67203152 67203152 single base substitution G A downstream_gene_variant MELA-AU 11 67203467 67203467 single base substitution C T downstream_gene_variant MELA-AU 11 67203771 67203772 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 67203822 67203822 single base substitution C T downstream_gene_variant MELA-AU 11 67203897 67203897 single base substitution A T downstream_gene_variant MELA-AU 11 67204624 67204625 multiple base substitution (>=2bp and <=200bp) TC CT downstream_gene_variant MELA-AU 11 67205025 67205025 single base substitution G A downstream_gene_variant MELA-AU 11 67205292 67205292 single base substitution G A downstream_gene_variant MELA-AU 11 67205411 67205411 single base substitution G A downstream_gene_variant MELA-AU 11 67205636 67205636 single base substitution G A 3_prime_UTR_variant MELA-AU 11 67205636 67205636 single base substitution G A downstream_gene_variant MELA-AU 11 67206608 67206608 single base substitution G A downstream_gene_variant MELA-AU 11 67206608 67206608 single base substitution G A intron_variant MELA-AU 11 67209021 67209021 single base substitution G A 3_prime_UTR_variant MELA-AU 11 67209021 67209021 single base substitution G A downstream_gene_variant MELA-AU 11 67209021 67209021 single base substitution G A intron_variant MELA-AU 11 67209021 67209021 single base substitution G A upstream_gene_variant MELA-AU 11 67209959 67209959 single base substitution G A exon_variant MELA-AU 11 67209959 67209959 single base substitution G A synonymous_variant F47F 141C>T MELA-AU 11 67209959 67209959 single base substitution G A upstream_gene_variant MELA-AU 11 67210068 67210068 single base substitution T C exon_variant MELA-AU 11 67210068 67210068 single base substitution T C missense_variant K11R 32A>G MELA-AU 11 67210068 67210068 single base substitution T C upstream_gene_variant MELA-AU 11 67210823 67210823 single base substitution G A intron_variant MELA-AU 11 67210823 67210823 single base substitution G A upstream_gene_variant MELA-AU 11 67211353 67211353 single base substitution C T upstream_gene_variant MELA-AU 11 67211770 67211770 single base substitution T C upstream_gene_variant MELA-AU 11 67212473 67212473 single base substitution C T upstream_gene_variant MELA-AU 11 67212595 67212595 single base substitution G A upstream_gene_variant MELA-AU 11 67212668 67212668 single base substitution C T upstream_gene_variant MELA-AU 11 67212788 67212788 single base substitution C T upstream_gene_variant MELA-AU 11 67212971 67212972 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 67213000 67213000 single base substitution C T upstream_gene_variant MELA-AU 11 67213050 67213050 single base substitution G A upstream_gene_variant MELA-AU 11 67213723 67213723 single base substitution C T upstream_gene_variant MELA-AU 11 67214441 67214441 single base substitution C T upstream_gene_variant MELA-AU 11 67214462 67214462 single base substitution C T upstream_gene_variant MELA-AU 11 67214616 67214616 single base substitution C T upstream_gene_variant MELA-AU 11 67214622 67214622 single base substitution G A upstream_gene_variant MELA-AU 11 67214891 67214891 single base substitution G A upstream_gene_variant MELA-AU 11 67214915 67214915 single base substitution G A upstream_gene_variant MELA-AU 11 67215291 67215291 single base substitution C T upstream_gene_variant MELA-AU 11 67215685 67215686 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 67215687 67215687 single base substitution C A upstream_gene_variant MELA-AU 11 67215934 67215934 single base substitution C T upstream_gene_variant OV-AU 11 67201964 67201964 insertion of <=200bp - G downstream_gene_variant OV-AU 11 67205600 67205600 single base substitution G A 3_prime_UTR_variant OV-AU 11 67205600 67205600 single base substitution G A downstream_gene_variant OV-AU 11 67209664 67209664 single base substitution C T intron_variant OV-AU 11 67209664 67209664 single base substitution C T upstream_gene_variant OV-AU 11 67210735 67210735 single base substitution G T intron_variant OV-AU 11 67210735 67210735 single base substitution G T upstream_gene_variant OV-AU 11 67210932 67210932 single base substitution G C 5_prime_UTR_variant OV-AU 11 67210932 67210932 single base substitution G C exon_variant OV-AU 11 67210932 67210932 single base substitution G C upstream_gene_variant OV-AU 11 67213339 67213339 single base substitution G C upstream_gene_variant OV-AU 11 67215913 67215913 single base substitution G T upstream_gene_variant PACA-AU 11 67212446 67212446 single base substitution C T upstream_gene_variant PACA-CA 11 67200566 67200566 single base substitution G A downstream_gene_variant PACA-CA 11 67200687 67200687 single base substitution G A downstream_gene_variant PACA-CA 11 67201087 67201087 single base substitution T A downstream_gene_variant PACA-CA 11 67201419 67201419 single base substitution A G downstream_gene_variant PACA-CA 11 67203591 67203591 single base substitution C T downstream_gene_variant PACA-CA 11 67207359 67207359 single base substitution C A downstream_gene_variant PACA-CA 11 67207359 67207359 single base substitution C A intron_variant PACA-CA 11 67207600 67207600 single base substitution G A 3_prime_UTR_variant PACA-CA 11 67207600 67207600 single base substitution G A downstream_gene_variant PACA-CA 11 67207600 67207600 single base substitution G A intron_variant PACA-CA 11 67207600 67207600 single base substitution G A synonymous_variant C332C 996C>T PACA-CA 11 67208489 67208489 single base substitution C G downstream_gene_variant PACA-CA 11 67208489 67208489 single base substitution C G intron_variant PACA-CA 11 67208489 67208489 single base substitution C G missense_variant G288A 863G>C PACA-CA 11 67208489 67208489 single base substitution C G upstream_gene_variant PACA-CA 11 67212162 67212162 insertion of <=200bp - T upstream_gene_variant PACA-CA 11 67214335 67214335 single base substitution T A upstream_gene_variant PACA-CA 11 67214336 67214336 single base substitution C A upstream_gene_variant PBCA-DE 11 67209167 67209167 single base substitution T G downstream_gene_variant PBCA-DE 11 67209167 67209167 single base substitution T G intron_variant PBCA-DE 11 67209167 67209167 single base substitution T G missense_variant H164P 491A>C PBCA-DE 11 67209167 67209167 single base substitution T G upstream_gene_variant PRAD-US 11 67205932 67205932 single base substitution G T 3_prime_UTR_variant PRAD-US 11 67205932 67205932 single base substitution G T downstream_gene_variant PRAD-US 11 67205932 67205932 single base substitution G T exon_variant PRAD-US 11 67205932 67205932 single base substitution G T missense_variant A462D 1385C>A READ-US 11 67208923 67208923 single base substitution T C 3_prime_UTR_variant READ-US 11 67208923 67208923 single base substitution T C downstream_gene_variant READ-US 11 67208923 67208923 single base substitution T C exon_variant READ-US 11 67208923 67208923 single base substitution T C missense_variant S173G 517A>G READ-US 11 67208923 67208923 single base substitution T C upstream_gene_variant RECA-EU 11 67201342 67201342 single base substitution G A downstream_gene_variant RECA-EU 11 67206176 67206176 single base substitution T C 3_prime_UTR_variant RECA-EU 11 67206176 67206176 single base substitution T C downstream_gene_variant RECA-EU 11 67206176 67206176 single base substitution T C exon_variant RECA-EU 11 67206176 67206176 single base substitution T C missense_variant D437G 1310A>G RECA-EU 11 67207245 67207245 single base substitution G A downstream_gene_variant RECA-EU 11 67207245 67207245 single base substitution G A intron_variant RECA-EU 11 67208677 67208677 single base substitution C G downstream_gene_variant RECA-EU 11 67208677 67208677 single base substitution C G exon_variant RECA-EU 11 67208677 67208677 single base substitution C G synonymous_variant R225R 675G>C RECA-EU 11 67208677 67208677 single base substitution C G upstream_gene_variant RECA-EU 11 67214060 67214060 single base substitution T C upstream_gene_variant SKCA-BR 11 67201728 67201728 single base substitution C T downstream_gene_variant SKCA-BR 11 67201729 67201729 single base substitution C T downstream_gene_variant SKCA-BR 11 67211112 67211112 single base substitution C A exon_variant SKCA-BR 11 67211112 67211112 single base substitution C A intron_variant SKCA-BR 11 67211112 67211112 single base substitution C A upstream_gene_variant SKCA-BR 11 67211155 67211155 single base substitution A G intron_variant SKCA-BR 11 67211155 67211155 single base substitution A G upstream_gene_variant SKCA-BR 11 67213041 67213041 single base substitution T C upstream_gene_variant SKCA-BR 11 67213107 67213107 single base substitution A C upstream_gene_variant SKCA-BR 11 67215105 67215105 single base substitution C T upstream_gene_variant SKCM-US 11 67200847 67200847 single base substitution G A downstream_gene_variant SKCM-US 11 67200855 67200855 single base substitution C T downstream_gene_variant SKCM-US 11 67201482 67201482 single base substitution C T downstream_gene_variant SKCM-US 11 67207678 67207678 single base substitution G A 3_prime_UTR_variant SKCM-US 11 67207678 67207678 single base substitution G A downstream_gene_variant SKCM-US 11 67207678 67207678 single base substitution G A synonymous_variant F306F 918C>T SKCM-US 11 67207678 67207678 single base substitution G A upstream_gene_variant SKCM-US 11 67210079 67210079 single base substitution G A exon_variant SKCM-US 11 67210079 67210079 single base substitution G A synonymous_variant V7V 21C>T SKCM-US 11 67210079 67210079 single base substitution G A upstream_gene_variant STAD-US 11 67200863 67200863 single base substitution G T downstream_gene_variant STAD-US 11 67201739 67201739 single base substitution C A downstream_gene_variant STAD-US 11 67201891 67201891 single base substitution G A downstream_gene_variant STAD-US 11 67201901 67201901 single base substitution G A downstream_gene_variant STAD-US 11 67201943 67201943 single base substitution C T downstream_gene_variant STAD-US 11 67203412 67203412 single base substitution G A downstream_gene_variant STAD-US 11 67203517 67203517 single base substitution T C downstream_gene_variant STAD-US 11 67207611 67207611 single base substitution C T 3_prime_UTR_variant STAD-US 11 67207611 67207611 single base substitution C T downstream_gene_variant STAD-US 11 67207611 67207611 single base substitution C T missense_variant V329I 985G>A STAD-US 11 67207611 67207611 single base substitution C T splice_donor_variant STAD-US 11 67208620 67208620 single base substitution C T downstream_gene_variant STAD-US 11 67208620 67208620 single base substitution C T exon_variant STAD-US 11 67208620 67208620 single base substitution C T synonymous_variant E244E 732G>A STAD-US 11 67208620 67208620 single base substitution C T upstream_gene_variant STAD-US 11 67208646 67208646 single base substitution T C downstream_gene_variant STAD-US 11 67208646 67208646 single base substitution T C exon_variant STAD-US 11 67208646 67208646 single base substitution T C missense_variant T236A 706A>G STAD-US 11 67208646 67208646 single base substitution T C upstream_gene_variant STAD-US 11 67208687 67208687 single base substitution C T downstream_gene_variant STAD-US 11 67208687 67208687 single base substitution C T exon_variant STAD-US 11 67208687 67208687 single base substitution C T missense_variant R222Q 665G>A STAD-US 11 67208687 67208687 single base substitution C T upstream_gene_variant STAD-US 11 67208817 67208817 single base substitution C T 3_prime_UTR_variant STAD-US 11 67208817 67208817 single base substitution C T downstream_gene_variant STAD-US 11 67208817 67208817 single base substitution C T exon_variant STAD-US 11 67208817 67208817 single base substitution C T missense_variant G208D 623G>A STAD-US 11 67208817 67208817 single base substitution C T upstream_gene_variant THCA-US 11 67201890 67201890 single base substitution C T downstream_gene_variant UCEC-US 11 67201701 67201701 single base substitution C T downstream_gene_variant UCEC-US 11 67201718 67201718 single base substitution G A downstream_gene_variant UCEC-US 11 67202510 67202510 single base substitution C T downstream_gene_variant UCEC-US 11 67202553 67202553 single base substitution G A downstream_gene_variant UCEC-US 11 67203361 67203361 single base substitution G A downstream_gene_variant UCEC-US 11 67203434 67203434 single base substitution C T downstream_gene_variant UCEC-US 11 67207718 67207718 single base substitution C T 3_prime_UTR_variant UCEC-US 11 67207718 67207718 single base substitution C T downstream_gene_variant UCEC-US 11 67207718 67207718 single base substitution C T exon_variant UCEC-US 11 67207718 67207718 single base substitution C T missense_variant R293Q 878G>A UCEC-US 11 67207718 67207718 single base substitution C T upstream_gene_variant UCEC-US 11 67208620 67208620 single base substitution C T downstream_gene_variant UCEC-US 11 67208620 67208620 single base substitution C T exon_variant UCEC-US 11 67208620 67208620 single base substitution C T synonymous_variant E244E 732G>A UCEC-US 11 67208620 67208620 single base substitution C T upstream_gene_variant UCEC-US 11 67208702 67208702 single base substitution G A downstream_gene_variant UCEC-US 11 67208702 67208702 single base substitution G A exon_variant UCEC-US 11 67208702 67208702 single base substitution G A missense_variant A217V 650C>T UCEC-US 11 67208702 67208702 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T2940 COSM4674227 c.1320delC p.S441fs*16 Deletion - Frameshift 11:67438695-67438695 - Pat_55_A COSM5839377 c.485delT p.V162fs*81 Deletion - Frameshift 11:67441484-67441484 - SCC-9 COSM4591122 c.1282G>C p.A428P Substitution - Missense 11:67438733-67438733 - UM-SCC-2 COSM4591122 c.1282G>C p.A428P Substitution - Missense 11:67438733-67438733 - TCGA-AC-A3OD-01 COSM5831841 c.1287delC p.A430fs*27 Deletion - Frameshift 11:67438728-67438728 - KYSE-140 COSM2041967 c.1204C>T p.R402W Substitution - Missense 11:67438811-67438811 - TCGA-AH-6897-01 COSM3416171 c.517A>G p.S173G Substitution - Missense 11:67441452-67441452 - 587332 COSM1202094 c.1344+2T>C p.? Unknown 11:67438669-67438669 - TCGA-AP-A0LT-01 COSM931086 c.650C>T p.A217V Substitution - Missense 11:67441231-67441231 - PD4109a COSM3355818 c.1432G>C p.E478Q Substitution - Missense 11:67438414-67438414 - BN04T COSM1605113 c.1026G>T p.E342D Substitution - Missense 11:67439825-67439825 - Mx43 COSM32982 c.1231G>A p.V411M Substitution - Missense 11:67438784-67438784 - WSU-HN30 COSM4593482 c.1270T>C p.S424P Substitution - Missense 11:67438745-67438745 - CSCC-35-T COSM4525977 c.1366G>A p.V456M Substitution - Missense 11:67438480-67438480 - PD4109a COSM3355818 c.1432G>C p.E478Q Substitution - Missense 11:67438414-67438414 - S00837 COSM310288 c.809C>A p.A270D Substitution - Missense 11:67440387-67440387 - UD-SCC-2 COSM4593482 c.1270T>C p.S424P Substitution - Missense 11:67438745-67438745 - T6 COSM5341704 c.114C>T p.S38S Substitution - coding silent 11:67442515-67442515 - S00501 COSM310287 c.786G>T p.Q262H Substitution - Missense 11:67440410-67440410 - TCGA-B6-A0IN-01 COSM5831842 c.977_978insG p.L327fs*16 Insertion - Frameshift 11:67440147-67440148 - 585208 COSM325051 c.38G>T p.R13L Substitution - Missense 11:67442591-67442591 - CSCC-31-T COSM4405316 c.21C>T p.V7V Substitution - coding silent 11:67442608-67442608 - S02292 COSM5687307 c.847T>G p.Y283D Substitution - Missense 11:67440349-67440349 - 587350 COSM1202095 c.209G>A p.R70H Substitution - Missense 11:67442081-67442081 - TCGA-A6-6654-01 COSM3687585 c.477C>T p.I159I Substitution - coding silent 11:67441492-67441492 - UM-SCC-2 COSM4593482 c.1270T>C p.S424P Substitution - Missense 11:67438745-67438745 - HCT8 COSM4633401 c.661G>A p.A221T Substitution - Missense 11:67441220-67441220 - TCGA-D1-A17H-01 COSM931085 c.732G>A p.E244E Substitution - coding silent 11:67441149-67441149 - RKO COSM2041965 c.1426C>T p.R476C Substitution - Missense 11:67438420-67438420 - CSCC-19-T COSM4518511 c.675_676GG>AA p.A226T Substitution - Missense 11:67441205-67441206 - TCGA-BR-4256-01 COSM4035994 c.706A>G p.T236A Substitution - Missense 11:67441175-67441175 - TCGA-B0-5098-01 COSM1492683 c.954T>C p.G318G Substitution - coding silent 11:67440171-67440171 - TCGA-CZ-5455-01 COSM3359361 c.974G>A p.R325Q Substitution - Missense 11:67440151-67440151 - PD11367a COSM4146200 c.982G>C p.E328Q Substitution - Missense 11:67440143-67440143 - TCGA-BR-8591-01 COSM4035998 c.623G>A p.G208D Substitution - Missense 11:67441346-67441346 - CSCC-44-T COSM4524284 c.1263G>A p.P421P Substitution - coding silent 11:67438752-67438752 - T368 COSM4674228 c.810C>T p.A270A Substitution - coding silent 11:67440386-67440386 - 587238 COSM1202093 c.89G>A p.R30H Substitution - Missense 11:67442540-67442540 - TCGA-25-1319-01 COSM70280 c.97C>T p.R33C Substitution - Missense 11:67442532-67442532 - RKO COSM2042014 c.11G>A p.R4H Substitution - Missense 11:67442618-67442618 - 19M COSM5578342 c.81G>A p.E27E Substitution - coding silent 11:67442548-67442548 - 93VU147T COSM4591122 c.1282G>C p.A428P Substitution - Missense 11:67438733-67438733 - CSCC-15-T COSM4505719 c.6C>A p.S2S Substitution - coding silent 11:67442623-67442623 - WSU-HN6 COSM4591122 c.1282G>C p.A428P Substitution - Missense 11:67438733-67438733 - CSCC-55-T COSM4561469 c.886G>A p.E296K Substitution - Missense 11:67440239-67440239 - PTC-28C COSM4146200 c.982G>C p.E328Q Substitution - Missense 11:67440143-67440143 - T3058 COSM4674229 c.640C>T p.R214W Substitution - Missense 11:67441241-67441241 - C0025T COSM4165928 c.675G>C p.R225R Substitution - coding silent 11:67441206-67441206 - TCGA-AD-6899-01 COSM1356420 c.459C>T p.C153C Substitution - coding silent 11:67441510-67441510 - TCGA-G2-A3VY-01 COSM690350 c.766G>C p.E256Q Substitution - Missense 11:67440430-67440430 - TCGA-BH-A18G-01 COSM1202095 c.209G>A p.R70H Substitution - Missense 11:67442081-67442081 - TCGA-FV-A23B-01 COSM4914108 c.53A>G p.Q18R Substitution - Missense 11:67442576-67442576 - PTC-53C COSM4146202 c.912C>A p.I304I Substitution - coding silent 11:67440213-67440213 - TCGA-AZ-6601-01 COSM1356421 c.286G>A p.E96K Substitution - Missense 11:67442004-67442004 - Pat_66_A COSM5839379 c.400C>T p.R134* Substitution - Nonsense 11:67441787-67441787 - TCGA-EE-A181-06 COSM3452299 c.918C>T p.F306F Substitution - coding silent 11:67440207-67440207 - UPCI:SCC090 COSM4593482 c.1270T>C p.S424P Substitution - Missense 11:67438745-67438745 - LIS03PT2 COSM1732298 c.1067C>T p.S356L Substitution - Missense 11:67438948-67438948 - ESO-250 COSM1248984 c.637-5G>A p.? Unknown 11:67441249-67441249 - ESCC_60 COSM5632677 c.520C>T p.L174L Substitution - coding silent 11:67441449-67441449 - TCGA-DR-A0ZM-01 COSM458427 c.619C>T p.R207W Substitution - Missense 11:67441350-67441350 - YUDEDE COSM1704293 c.754C>T p.P252S Substitution - Missense 11:67441127-67441127 - tumor_4176133 COSM3356241 c.1356G>A p.K452K Substitution - coding silent 11:67438490-67438490 - CCK81 COSM4620645 c.1287C>T p.P429P Substitution - coding silent 11:67438728-67438728 - ESO-169 COSM1248983 c.722G>A p.R241Q Substitution - Missense 11:67441159-67441159 - I2L-P25-Tumor-Organoid COSM5360890 c.1003G>A p.A335T Substitution - Missense 11:67440122-67440122 - 61 COSM5739349 c.22C>T p.R8W Substitution - Missense 11:67442607-67442607 - TCGA-AP-A059-01 COSM931084 c.878G>A p.R293Q Substitution - Missense 11:67440247-67440247 - S00501 COSM310287 c.786G>T p.Q262H Substitution - Missense 11:67440410-67440410 - 46M COSM5587542 c.191C>T p.P64L Substitution - Missense 11:67442438-67442438 - RXF393 COSM1676234 c.733C>T p.R245W Substitution - Missense 11:67441148-67441148 - TCGA-D9-A6EC-06 COSM4405316 c.21C>T p.V7V Substitution - coding silent 11:67442608-67442608 - PCSI_0302_Pa_P_526 COSM4808458 c.996C>T p.C332C Substitution - coding silent 11:67440129-67440129 - 408 COSM4430361 c.170G>A p.G57E Substitution - Missense 11:67442459-67442459 - S00837 COSM310288 c.809C>A p.A270D Substitution - Missense 11:67440387-67440387 - NOKSI COSM4591122 c.1282G>C p.A428P Substitution - Missense 11:67438733-67438733 - RK125_C01 COSM3700132 c.1095C>T p.P365P Substitution - coding silent 11:67438920-67438920 - TCGA-HU-8602-01 COSM4035996 c.665G>A p.R222Q Substitution - Missense 11:67441216-67441216 - PR-00-1165 COSM243819 c.832G>A p.D278N Substitution - Missense 11:67440364-67440364 - 18 COSM5745132 c.1322G>A p.S441N Substitution - Missense 11:67438693-67438693 - ESCC_77 COSM5635312 c.1045G>A p.V349I Substitution - Missense 11:67439806-67439806 - TCGA-D7-A4YV-01 COSM4035992 c.985G>A p.V329I Substitution - Missense 11:67440140-67440140 - CCK81 COSM4200111 c.429G>A p.T143T Substitution - coding silent 11:67441758-67441758 - T3535 COSM1202095 c.209G>A p.R70H Substitution - Missense 11:67442081-67442081 - TCGA-EJ-7785-01 COSM1470562 c.1385C>A p.A462D Substitution - Missense 11:67438461-67438461 - CN-AML-CR-67-Dx COSM5426889 c.1345-6C>T p.? Unknown 11:67438507-67438507 - PTC-14C COSM4146201 c.958G>T p.G320C Substitution - Missense 11:67440167-67440167 - SNU-175 COSM4650257 c.1226G>A p.R409H Substitution - Missense 11:67438789-67438789 - C0016T COSM4165927 c.1310A>G p.D437G Substitution - Missense 11:67438705-67438705 - HCT15 COSM4632576 c.1220G>A p.S407N Substitution - Missense 11:67438795-67438795 - LUAD-RT-S01709 COSM379844 c.1188C>G p.Y396* Substitution - Nonsense 11:67438827-67438827 - TCGA-AD-6895-01 COSM3687790 c.231G>A p.T77T Substitution - coding silent 11:67442059-67442059 - TCGA-BR-4368-01 COSM931085 c.732G>A p.E244E Substitution - coding silent 11:67441149-67441149 - TCGA-AD-5900-01 COSM1356419 c.855C>T p.C285C Substitution - coding silent 11:67440341-67440341 - TCGA-D1-A163-01 COSM931087 c.245C>T p.T82M Substitution - Missense 11:67442045-67442045 - pfg068T COSM4756791 c.466G>A p.V156M Substitution - Missense 11:67441503-67441503 - I2L-P7-Tumor-Organoid COSM243819 c.832G>A p.D278N Substitution - Missense 11:67440364-67440364 - TCGA-37-3783-01 COSM690350 c.766G>C p.E256Q Substitution - Missense 11:67440430-67440430 - UM-SCC-4 COSM4591122 c.1282G>C p.A428P Substitution - Missense 11:67438733-67438733 - BICR_22 COSM4593482 c.1270T>C p.S424P Substitution - Missense 11:67438745-67438745 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.6181;Hs.6191 11q13.2 609849 1511761|dbSNP|BC006449|C/T|non-coding||1749|Confirmed

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer CA AG Missense p.W184L c.550_551delinsCT 11 67208889 CM C A Missense p.Q262H c.786G>T 11 67207881 SCLC C A Missense p.R13L c.38G>T 11 67210062 SCLC CC AT Missense p.G471I c.1411_1412delinsAT 11 67205905 CM C G Missense p.E256Q c.766G>C 11 67207901 LUSC C T Missense p.R241Q c.722G>A 11 67208630 ESCA C T Missense p.R325Q c.974G>A 11 67207622 RCCC C T Missense p.V147M c.439G>A 11 67209219 LUAD C T Synonymous p.E244E c.732G>A 11 67208620 STAD C T Synonymous p.E244E c.732G>A 11 67208620 UCEC C T Synonymous p.R207R c.621G>A 11 67208819 STAD G A Missense p.A217V c.650C>T 11 67208702 UCEC G A Missense p.R33C c.97C>T 11 67210003 OV G A Missense p.V411M c.1231G>A 11 67206255 COREAD G A Synonymous p.F306F c.918C>T 11 67207678 CM - G Frameshift p.A430Rfs*8 c.1287dupC 11 67206199 THCA GG - IntronicDeletion . c.454+35_454+36delCC 11 67209168 STAD G - IntronicDeletion . c.454+36delC 11 67209168 STAD G T IntronicSNV . c.454+36C>A 11 67209168 RCCC G T Missense p.A270D c.809C>A 11 67207858 SCLC G T Missense p.A462D c.1385C>A 11 67205932 PRAD G T Missense p.P120Q c.359C>A 11 67209299 STAD T C Missense p.T236A c.706A>G 11 67208646 STAD