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 47202120 47202120 + Silent SNP G G A TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr11:47202120G>A c.333C>T c.(331-333)cgC>cgT p.R111R BLCA 11 47199592 47199592 + Nonsense_Mutation SNP C C A TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr11:47199592C>A c.1165G>T c.(1165-1167)Gag>Tag p.E389* BLCA 11 47200713 47200713 + Silent SNP G G A TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr11:47200713G>A c.897C>T c.(895-897)ttC>ttT p.F299F BLCA 11 47201023 47201023 + Missense_Mutation SNP G G C TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr11:47201023G>C c.718C>G c.(718-720)Ctt>Gtt p.L240V BLCA 11 47201080 47201080 + Missense_Mutation SNP T T C TCGA-FD-A5C0-01A-11D-A289-08 TCGA-FD-A5C0-10A-01D-A289-08 g.chr11:47201080T>C c.661A>G c.(661-663)Atg>Gtg p.M221V BLCA 11 47201746 47201746 + Missense_Mutation SNP C C G TCGA-GC-A6I1-01A-12D-A31L-08 TCGA-GC-A6I1-10A-01D-A31J-08 g.chr11:47201746C>G c.594G>C c.(592-594)gaG>gaC p.E198D BLCA 11 47201882 47201882 + Missense_Mutation SNP G G A TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr11:47201882G>A c.458C>T c.(457-459)tCc>tTc p.S153F BLCA 11 47202146 47202146 + Nonsense_Mutation SNP G G A TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr11:47202146G>A c.307C>T c.(307-309)Caa>Taa p.Q103* BLCA 11 47204266 47204266 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr11:47204266C>G c.13G>C c.(13-15)Gag>Cag p.E5Q BRCA 11 47200771 47200771 + Missense_Mutation SNP T T C TCGA-GM-A5PV-01A-11D-A28B-09 TCGA-GM-A5PV-10A-01D-A28E-09 g.chr11:47200771T>C c.839A>G c.(838-840)gAt>gGt p.D280G BRCA 11 47201107 47201108 + Missense_Mutation DNP CT CT TG TCGA-BH-A0HP-01A-12D-A099-09 TCGA-BH-A0HP-10A-01D-A099-09 g.chr11:47201107_47201108CT>TG c.633_634AG>CA c.(631-636)gcAGag>gcCAag p.E212K CESC 11 47200581 47200581 + Splice_Site SNP C C T TCGA-JW-A5VJ-01A-11D-A28B-09 TCGA-JW-A5VJ-10A-01D-A28E-09 g.chr11:47200581C>T c.901G>A c.(901-903)Gag>Aag p.E301K CESC 11 47204045 47204045 + Silent SNP G G A TCGA-C5-A7UC-01A-11D-A351-09 TCGA-C5-A7UC-10A-01D-A351-09 g.chr11:47204045G>A c.120C>T c.(118-120)gtC>gtT p.V40V COAD 11 47199529 47199529 + Missense_Mutation SNP G G A TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr11:47199529G>A c.1228C>T c.(1228-1230)Cgc>Tgc p.R410C COAD 11 47199595 47199595 + Frame_Shift_Del DEL C C - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:47199595delC c.1162delG c.(1162-1164)gagfs p.E389fs COAD 11 47199973 47199973 + Missense_Mutation SNP A A G TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr11:47199973A>G c.1103T>C c.(1102-1104)gTg>gCg p.V368A COAD 11 47200991 47200991 + Silent SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr11:47200991G>A c.750C>T c.(748-750)caC>caT p.H250H COAD 11 47202044 47202044 + Missense_Mutation SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr11:47202044G>A c.409C>T c.(409-411)Cgc>Tgc p.R137C COAD 11 47204026 47204026 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:47204026C>T c.139G>A c.(139-141)Gcc>Acc p.A47T COADREAD 11 47199529 47199529 + Missense_Mutation SNP G G A TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr11:47199529G>A c.1228C>T c.(1228-1230)Cgc>Tgc p.R410C COADREAD 11 47199595 47199595 + Frame_Shift_Del DEL C C - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:47199595delC c.1162delG c.(1162-1164)gagfs p.E389fs COADREAD 11 47199973 47199973 + Missense_Mutation SNP A A G TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr11:47199973A>G c.1103T>C c.(1102-1104)gTg>gCg p.V368A COADREAD 11 47200991 47200991 + Silent SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr11:47200991G>A c.750C>T c.(748-750)caC>caT p.H250H COADREAD 11 47202044 47202044 + Missense_Mutation SNP G G A TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr11:47202044G>A c.409C>T c.(409-411)Cgc>Tgc p.R137C COADREAD 11 47204026 47204026 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:47204026C>T c.139G>A c.(139-141)Gcc>Acc p.A47T GBMLGG 11 47201080 47201080 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:47201080T>C c.661A>G c.(661-663)Atg>Gtg p.M221V GBMLGG 11 47202192 47202192 + Silent SNP C C T TCGA-HW-8320-01A-11D-2395-08 TCGA-HW-8320-10A-01D-2396-08 g.chr11:47202192C>T c.261G>A c.(259-261)gcG>gcA p.A87A GBMLGG 11 47202229 47202229 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:47202229C>A c.224G>T c.(223-225)gGc>gTc p.G75V HNSC 11 47199930 47199930 + Silent SNP C C A TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr11:47199930C>A c.1146G>T c.(1144-1146)ctG>ctT p.L382L HNSC 11 47200530 47200530 + Missense_Mutation SNP G G A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr11:47200530G>A c.952C>T c.(952-954)Cgg>Tgg p.R318W HNSC 11 47200778 47200778 + Missense_Mutation SNP C C T TCGA-CQ-5334-01A-01D-1683-08 TCGA-CQ-5334-10A-01D-1683-08 g.chr11:47200778C>T c.832G>A c.(832-834)Gaa>Aaa p.E278K HNSC 11 47201009 47201009 + Silent SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:47201009A>G c.732T>C c.(730-732)gaT>gaC p.D244D KIPAN 11 47200712 47200712 + Missense_Mutation SNP C C T TCGA-BP-4760-01A-02D-1421-08 TCGA-BP-4760-11A-01D-1421-08 g.chr11:47200712C>T c.898G>A c.(898-900)Gag>Aag p.E300K KIRC 11 47200712 47200712 + Missense_Mutation SNP C C T TCGA-BP-4760-01A-02D-1421-08 TCGA-BP-4760-11A-01D-1421-08 g.chr11:47200712C>T c.898G>A c.(898-900)Gag>Aag p.E300K LGG 11 47201080 47201080 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:47201080T>C c.661A>G c.(661-663)Atg>Gtg p.M221V LGG 11 47202192 47202192 + Silent SNP C C T TCGA-HW-8320-01A-11D-2395-08 TCGA-HW-8320-10A-01D-2396-08 g.chr11:47202192C>T c.261G>A c.(259-261)gcG>gcA p.A87A LGG 11 47202229 47202229 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:47202229C>A c.224G>T c.(223-225)gGc>gTc p.G75V LIHC 11 47199984 47199984 + Silent SNP G G T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr11:47199984G>T c.1092C>A c.(1090-1092)acC>acA p.T364T LIHC 11 47201773 47201773 + Missense_Mutation SNP C C A TCGA-CC-A7II-01A-11D-A33K-10 TCGA-CC-A7II-10A-01D-A33K-10 g.chr11:47201773C>A c.567G>T c.(565-567)caG>caT p.Q189H LIHC 11 47201777 47201777 + Missense_Mutation SNP A A T TCGA-DD-AACN-01A-11D-A40R-10 TCGA-DD-AACN-10A-01D-A40U-10 g.chr11:47201777A>T c.563T>A c.(562-564)cTg>cAg p.L188Q LIHC 11 47201829 47201829 + Nonsense_Mutation SNP C C A TCGA-DD-AADQ-01A-11D-A40R-10 TCGA-DD-AADQ-10A-01D-A40U-10 g.chr11:47201829C>A c.511G>T c.(511-513)Gag>Tag p.E171* LUAD 11 47199559 47199559 + Missense_Mutation SNP C C T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr11:47199559C>T c.1198G>A c.(1198-1200)Ggc>Agc p.G400S LUAD 11 47201066 47201066 + Missense_Mutation SNP T T A TCGA-86-7713-01A-11D-2063-08 TCGA-86-7713-10A-01D-2063-08 g.chr11:47201066T>A c.675A>T c.(673-675)gaA>gaT p.E225D LUAD 11 47203976 47203976 + Missense_Mutation SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr11:47203976C>A c.189G>T c.(187-189)aaG>aaT p.K63N LUAD 11 47204066 47204066 + Silent SNP G G A TCGA-44-6144-01A-11D-1753-08 TCGA-44-6144-10A-01D-1753-08 g.chr11:47204066G>A c.99C>T c.(97-99)caC>caT p.H33H OV 11 47201085 47201085 + Missense_Mutation SNP C C T TCGA-61-2614-01A-01W-1092-09 TCGA-61-2614-10A-01W-1092-09 g.chr11:47201085C>T c.656G>A c.(655-657)cGc>cAc p.R219H PAAD 11 47203984 47203984 + Missense_Mutation SNP C C T TCGA-IB-7885-01A-11D-2154-08 TCGA-IB-7885-10A-01D-2154-08 g.chr11:47203984C>T c.181G>A c.(181-183)Gcc>Acc p.A61T SARC 11 47199923 47199923 + Nonsense_Mutation SNP G G A TCGA-DX-A8BG-01A-12D-A417-09 TCGA-DX-A8BG-10B-01D-A41A-09 g.chr11:47199923G>A c.1153C>T c.(1153-1155)Cga>Tga p.R385* SKCM 11 47202098 47202098 + Missense_Mutation SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr11:47202098G>A c.355C>T c.(355-357)Cac>Tac p.H119Y SKCM 11 47203992 47203992 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr11:47203992G>A c.173C>T c.(172-174)gCt>gTt p.A58V

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 47202191 47202191 single base substitution C T 5_prime_UTR_variant BLCA-CN 11 47202191 47202191 single base substitution C T downstream_gene_variant BLCA-CN 11 47202191 47202191 single base substitution C T exon_variant BLCA-CN 11 47202191 47202191 single base substitution C T missense_variant A88T 262G>A BLCA-CN 11 47202191 47202191 single base substitution C T upstream_gene_variant BLCA-US 11 47198344 47198344 single base substitution G C downstream_gene_variant BRCA-EU 11 47194552 47194552 single base substitution G C downstream_gene_variant BRCA-EU 11 47194619 47194619 single base substitution G C downstream_gene_variant BRCA-EU 11 47198946 47198946 single base substitution A G downstream_gene_variant BRCA-EU 11 47199770 47199770 single base substitution G C downstream_gene_variant BRCA-EU 11 47199770 47199770 single base substitution G C intron_variant BRCA-EU 11 47201002 47201002 single base substitution G A downstream_gene_variant BRCA-EU 11 47201002 47201002 single base substitution G A exon_variant BRCA-EU 11 47201002 47201002 single base substitution G A missense_variant L247F 739C>T BRCA-EU 11 47201002 47201002 single base substitution G A missense_variant L27F 79C>T BRCA-EU 11 47201002 47201002 single base substitution G A upstream_gene_variant BRCA-EU 11 47201375 47201375 single base substitution G A downstream_gene_variant BRCA-EU 11 47201375 47201375 single base substitution G A intron_variant BRCA-EU 11 47201375 47201375 single base substitution G A upstream_gene_variant BRCA-EU 11 47201471 47201471 single base substitution C G downstream_gene_variant BRCA-EU 11 47201471 47201471 single base substitution C G intron_variant BRCA-EU 11 47201471 47201471 single base substitution C G upstream_gene_variant BRCA-EU 11 47202107 47202107 single base substitution C A 5_prime_UTR_variant BRCA-EU 11 47202107 47202107 single base substitution C A downstream_gene_variant BRCA-EU 11 47202107 47202107 single base substitution C A exon_variant BRCA-EU 11 47202107 47202107 single base substitution C A missense_variant G116W 346G>T BRCA-EU 11 47202107 47202107 single base substitution C A upstream_gene_variant BRCA-EU 11 47202813 47202813 insertion of <=200bp - A downstream_gene_variant BRCA-EU 11 47202813 47202813 insertion of <=200bp - A intron_variant BRCA-EU 11 47202813 47202813 insertion of <=200bp - A upstream_gene_variant BRCA-EU 11 47203425 47203425 single base substitution C A downstream_gene_variant BRCA-EU 11 47203425 47203425 single base substitution C A intron_variant BRCA-EU 11 47203425 47203425 single base substitution C A upstream_gene_variant BRCA-EU 11 47203629 47203629 single base substitution G A downstream_gene_variant BRCA-EU 11 47203629 47203629 single base substitution G A intron_variant BRCA-EU 11 47203629 47203629 single base substitution G A upstream_gene_variant BRCA-EU 11 47203876 47203876 single base substitution C G downstream_gene_variant BRCA-EU 11 47203876 47203876 single base substitution C G intron_variant BRCA-EU 11 47203876 47203876 single base substitution C G upstream_gene_variant BRCA-EU 11 47205210 47205210 single base substitution C T intron_variant BRCA-EU 11 47205210 47205210 single base substitution C T upstream_gene_variant BRCA-EU 11 47205818 47205818 single base substitution G A intron_variant BRCA-EU 11 47205818 47205818 single base substitution G A upstream_gene_variant BRCA-EU 11 47206836 47206836 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 11 47206836 47206836 single base substitution G A intron_variant BRCA-EU 11 47206836 47206836 single base substitution G A upstream_gene_variant BRCA-EU 11 47209495 47209495 single base substitution T G upstream_gene_variant BRCA-EU 11 47210858 47210858 single base substitution C T upstream_gene_variant BRCA-EU 11 47211038 47211038 single base substitution C G upstream_gene_variant BRCA-EU 11 47211277 47211277 single base substitution G A upstream_gene_variant BRCA-EU 11 47212310 47212310 single base substitution G A upstream_gene_variant BRCA-EU 11 47212869 47212869 single base substitution C G upstream_gene_variant BRCA-FR 11 47202107 47202107 single base substitution C A 5_prime_UTR_variant BRCA-FR 11 47202107 47202107 single base substitution C A downstream_gene_variant BRCA-FR 11 47202107 47202107 single base substitution C A exon_variant BRCA-FR 11 47202107 47202107 single base substitution C A missense_variant G116W 346G>T BRCA-FR 11 47202107 47202107 single base substitution C A upstream_gene_variant BRCA-FR 11 47203488 47203488 single base substitution G C downstream_gene_variant BRCA-FR 11 47203488 47203488 single base substitution G C intron_variant BRCA-FR 11 47203488 47203488 single base substitution G C upstream_gene_variant BRCA-FR 11 47204316 47204316 single base substitution C A 5_prime_UTR_variant BRCA-FR 11 47204316 47204316 single base substitution C A intron_variant BRCA-FR 11 47204316 47204316 single base substitution C A splice_acceptor_variant BRCA-FR 11 47204316 47204316 single base substitution C A upstream_gene_variant BRCA-FR 11 47205210 47205210 single base substitution C T intron_variant BRCA-FR 11 47205210 47205210 single base substitution C T upstream_gene_variant BRCA-FR 11 47209495 47209495 single base substitution T G upstream_gene_variant BRCA-UK 11 47195350 47195350 single base substitution G A downstream_gene_variant BRCA-UK 11 47198384 47198384 single base substitution C T downstream_gene_variant BRCA-US 11 47198382 47198382 single base substitution G A downstream_gene_variant BRCA-US 11 47200771 47200771 single base substitution T C downstream_gene_variant BRCA-US 11 47200771 47200771 single base substitution T C exon_variant BRCA-US 11 47200771 47200771 single base substitution T C missense_variant D280G 839A>G BRCA-US 11 47200771 47200771 single base substitution T C missense_variant D2G 5A>G BRCA-US 11 47201107 47201107 single base substitution C T 5_prime_UTR_variant BRCA-US 11 47201107 47201107 single base substitution C T downstream_gene_variant BRCA-US 11 47201107 47201107 single base substitution C T exon_variant BRCA-US 11 47201107 47201107 single base substitution C T missense_variant E212K 634G>A BRCA-US 11 47201107 47201107 single base substitution C T upstream_gene_variant BRCA-US 11 47201108 47201108 single base substitution T G 5_prime_UTR_variant BRCA-US 11 47201108 47201108 single base substitution T G downstream_gene_variant BRCA-US 11 47201108 47201108 single base substitution T G exon_variant BRCA-US 11 47201108 47201108 single base substitution T G synonymous_variant A211A 633A>C BRCA-US 11 47201108 47201108 single base substitution T G upstream_gene_variant BTCA-JP 11 47194427 47194427 single base substitution A T downstream_gene_variant BTCA-JP 11 47195335 47195335 single base substitution C T downstream_gene_variant BTCA-JP 11 47196604 47196604 single base substitution C A downstream_gene_variant BTCA-JP 11 47198279 47198279 single base substitution C G downstream_gene_variant BTCA-JP 11 47199531 47199531 single base substitution C T 3_prime_UTR_variant BTCA-JP 11 47199531 47199531 single base substitution C T downstream_gene_variant BTCA-JP 11 47199531 47199531 single base substitution C T missense_variant G409D 1226G>A BTCA-JP 11 47200675 47200675 single base substitution C A downstream_gene_variant BTCA-JP 11 47200675 47200675 single base substitution C A intron_variant BTCA-JP 11 47200766 47200766 single base substitution G A downstream_gene_variant BTCA-JP 11 47200766 47200766 single base substitution G A exon_variant BTCA-JP 11 47200766 47200766 single base substitution G A missense_variant R282C 844C>T BTCA-JP 11 47200766 47200766 single base substitution G A missense_variant R4C 10C>T CESC-US 11 47200581 47200581 single base substitution C T downstream_gene_variant CESC-US 11 47200581 47200581 single base substitution C T missense_variant E23K 67G>A CESC-US 11 47200581 47200581 single base substitution C T missense_variant E301K 901G>A CESC-US 11 47200581 47200581 single base substitution C T splice_region_variant CESC-US 11 47204045 47204045 single base substitution G A 5_prime_UTR_variant CESC-US 11 47204045 47204045 single base substitution G A exon_variant CESC-US 11 47204045 47204045 single base substitution G A synonymous_variant V40V 120C>T CESC-US 11 47204045 47204045 single base substitution G A upstream_gene_variant COAD-US 11 47196853 47196853 deletion of <=200bp A - downstream_gene_variant COAD-US 11 47199595 47199595 deletion of <=200bp C - downstream_gene_variant COAD-US 11 47199595 47199595 deletion of <=200bp C - frameshift_variant E388 COAD-US 11 47199595 47199595 deletion of <=200bp C - frameshift_variant G69 COAD-US 11 47199595 47199595 deletion of <=200bp C - splice_region_variant COAD-US 11 47200991 47200991 single base substitution G A downstream_gene_variant COAD-US 11 47200991 47200991 single base substitution G A exon_variant COAD-US 11 47200991 47200991 single base substitution G A synonymous_variant H250H 750C>T COAD-US 11 47200991 47200991 single base substitution G A synonymous_variant H30H 90C>T COAD-US 11 47200991 47200991 single base substitution G A upstream_gene_variant COAD-US 11 47203983 47203983 single base substitution G A 5_prime_UTR_variant COAD-US 11 47203983 47203983 single base substitution G A exon_variant COAD-US 11 47203983 47203983 single base substitution G A missense_variant A61V 182C>T COAD-US 11 47203983 47203983 single base substitution G A upstream_gene_variant COAD-US 11 47204026 47204026 single base substitution C T 5_prime_UTR_variant COAD-US 11 47204026 47204026 single base substitution C T exon_variant COAD-US 11 47204026 47204026 single base substitution C T missense_variant A47T 139G>A COAD-US 11 47204026 47204026 single base substitution C T upstream_gene_variant COCA-CN 11 47199458 47199458 single base substitution G A 3_prime_UTR_variant COCA-CN 11 47199458 47199458 single base substitution G A downstream_gene_variant COCA-CN 11 47200509 47200509 single base substitution G T 3_prime_UTR_variant COCA-CN 11 47200509 47200509 single base substitution G T downstream_gene_variant COCA-CN 11 47200509 47200509 single base substitution G T missense_variant L325M 973C>A COCA-CN 11 47200509 47200509 single base substitution G T missense_variant L47M 139C>A COCA-CN 11 47200756 47200756 single base substitution C T downstream_gene_variant COCA-CN 11 47200756 47200756 single base substitution C T exon_variant COCA-CN 11 47200756 47200756 single base substitution C T missense_variant R285H 854G>A COCA-CN 11 47200756 47200756 single base substitution C T missense_variant R7H 20G>A COCA-CN 11 47204063 47204063 single base substitution C T 5_prime_UTR_variant COCA-CN 11 47204063 47204063 single base substitution C T exon_variant COCA-CN 11 47204063 47204063 single base substitution C T synonymous_variant R34R 102G>A COCA-CN 11 47204063 47204063 single base substitution C T upstream_gene_variant COCA-CN 11 47204280 47204280 single base substitution G A 5_prime_UTR_variant COCA-CN 11 47204280 47204280 single base substitution G A intron_variant COCA-CN 11 47204280 47204280 single base substitution G A upstream_gene_variant COCA-CN 11 47204787 47204787 single base substitution C T 5_prime_UTR_variant COCA-CN 11 47204787 47204787 single base substitution C T intron_variant COCA-CN 11 47204787 47204787 single base substitution C T upstream_gene_variant COCA-CN 11 47208982 47208982 single base substitution A G upstream_gene_variant ESAD-UK 11 47195115 47195115 single base substitution C T downstream_gene_variant ESAD-UK 11 47196726 47196726 single base substitution C T downstream_gene_variant ESAD-UK 11 47200435 47200435 single base substitution T C downstream_gene_variant ESAD-UK 11 47200435 47200435 single base substitution T C intron_variant ESAD-UK 11 47203729 47203729 single base substitution T C downstream_gene_variant ESAD-UK 11 47203729 47203729 single base substitution T C intron_variant ESAD-UK 11 47203729 47203729 single base substitution T C upstream_gene_variant ESAD-UK 11 47205504 47205504 single base substitution C G intron_variant ESAD-UK 11 47205504 47205504 single base substitution C G upstream_gene_variant ESAD-UK 11 47205808 47205808 single base substitution C T intron_variant ESAD-UK 11 47205808 47205808 single base substitution C T upstream_gene_variant ESAD-UK 11 47206768 47206771 deletion of <=200bp CGGG - intron_variant ESAD-UK 11 47206768 47206771 deletion of <=200bp CGGG - upstream_gene_variant ESAD-UK 11 47208204 47208204 single base substitution G A upstream_gene_variant ESAD-UK 11 47209980 47209980 deletion of <=200bp A - upstream_gene_variant ESAD-UK 11 47210342 47210342 single base substitution T C upstream_gene_variant ESCA-CN 11 47196783 47196783 single base substitution C T downstream_gene_variant GBM-US 11 47196824 47196824 single base substitution G C downstream_gene_variant KIRC-US 11 47195002 47195002 single base substitution A C downstream_gene_variant LAML-KR 11 47196748 47196748 single base substitution A C downstream_gene_variant LGG-US 11 47202192 47202192 single base substitution C T 5_prime_UTR_variant LGG-US 11 47202192 47202192 single base substitution C T downstream_gene_variant LGG-US 11 47202192 47202192 single base substitution C T exon_variant LGG-US 11 47202192 47202192 single base substitution C T synonymous_variant A87A 261G>A LGG-US 11 47202192 47202192 single base substitution C T upstream_gene_variant LICA-CN 11 47203958 47203958 single base substitution C A 5_prime_UTR_variant LICA-CN 11 47203958 47203958 single base substitution C A exon_variant LICA-CN 11 47203958 47203958 single base substitution C A missense_variant E69D 207G>T LICA-CN 11 47203958 47203958 single base substitution C A upstream_gene_variant LICA-FR 11 47196636 47196636 single base substitution T C downstream_gene_variant LICA-FR 11 47198875 47198875 single base substitution A C downstream_gene_variant LICA-FR 11 47199516 47199516 single base substitution T C 3_prime_UTR_variant LICA-FR 11 47199516 47199516 single base substitution T C downstream_gene_variant LICA-FR 11 47199516 47199516 single base substitution T C missense_variant Y414C 1241A>G LICA-FR 11 47202049 47202049 single base substitution C G 5_prime_UTR_variant LICA-FR 11 47202049 47202049 single base substitution C G downstream_gene_variant LICA-FR 11 47202049 47202049 single base substitution C G exon_variant LICA-FR 11 47202049 47202049 single base substitution C G missense_variant G135A 404G>C LICA-FR 11 47202049 47202049 single base substitution C G upstream_gene_variant LIHC-US 11 47195386 47195386 insertion of <=200bp - G downstream_gene_variant LIHC-US 11 47200816 47200816 single base substitution T C downstream_gene_variant LIHC-US 11 47200816 47200816 single base substitution T C exon_variant LIHC-US 11 47200816 47200816 single base substitution T C missense_variant H265R 794A>G LIHC-US 11 47200816 47200816 single base substitution T C missense_variant H45R 134A>G LIHC-US 11 47200816 47200816 single base substitution T C upstream_gene_variant LIHC-US 11 47201773 47201773 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant LIHC-US 11 47201773 47201773 single base substitution C A downstream_gene_variant LIHC-US 11 47201773 47201773 single base substitution C A exon_variant LIHC-US 11 47201773 47201773 single base substitution C A missense_variant Q189H 567G>T LIHC-US 11 47201773 47201773 single base substitution C A upstream_gene_variant LINC-JP 11 47194088 47194088 single base substitution A C downstream_gene_variant LINC-JP 11 47194731 47194731 single base substitution C A downstream_gene_variant LINC-JP 11 47194781 47194781 single base substitution C A downstream_gene_variant LINC-JP 11 47196497 47196497 single base substitution A T downstream_gene_variant LINC-JP 11 47198434 47198435 deletion of <=200bp TG - downstream_gene_variant LINC-JP 11 47201709 47201709 single base substitution G C downstream_gene_variant LINC-JP 11 47201709 47201709 single base substitution G C intron_variant LINC-JP 11 47201709 47201709 single base substitution G C upstream_gene_variant LINC-JP 11 47202120 47202120 single base substitution G A 5_prime_UTR_variant LINC-JP 11 47202120 47202120 single base substitution G A downstream_gene_variant LINC-JP 11 47202120 47202120 single base substitution G A exon_variant LINC-JP 11 47202120 47202120 single base substitution G A synonymous_variant R111R 333C>T LINC-JP 11 47202120 47202120 single base substitution G A upstream_gene_variant LINC-JP 11 47204533 47204533 deletion of <=200bp C - intron_variant LINC-JP 11 47204533 47204533 deletion of <=200bp C - upstream_gene_variant LINC-JP 11 47211533 47211533 single base substitution A C upstream_gene_variant LIRI-JP 11 47195210 47195210 single base substitution G T downstream_gene_variant LIRI-JP 11 47197008 47197008 single base substitution T C downstream_gene_variant LIRI-JP 11 47205878 47205878 single base substitution T G 5_prime_UTR_variant LIRI-JP 11 47205878 47205878 single base substitution T G intron_variant LIRI-JP 11 47205878 47205878 single base substitution T G upstream_gene_variant LIRI-JP 11 47206595 47206595 single base substitution C A intron_variant LIRI-JP 11 47206595 47206595 single base substitution C A upstream_gene_variant LIRI-JP 11 47209101 47209101 single base substitution C T upstream_gene_variant LUSC-KR 11 47198644 47198644 single base substitution G A downstream_gene_variant LUSC-KR 11 47202486 47202486 single base substitution G A downstream_gene_variant LUSC-KR 11 47202486 47202486 single base substitution G A intron_variant LUSC-KR 11 47202486 47202486 single base substitution G A upstream_gene_variant LUSC-KR 11 47203694 47203694 single base substitution C A downstream_gene_variant LUSC-KR 11 47203694 47203694 single base substitution C A intron_variant LUSC-KR 11 47203694 47203694 single base substitution C A upstream_gene_variant LUSC-KR 11 47209141 47209141 single base substitution G A upstream_gene_variant MALY-DE 11 47199834 47199834 single base substitution G A downstream_gene_variant MALY-DE 11 47199834 47199834 single base substitution G A intron_variant MALY-DE 11 47200368 47200368 single base substitution A C downstream_gene_variant MALY-DE 11 47200368 47200368 single base substitution A C intron_variant MALY-DE 11 47207365 47207365 single base substitution G A 5_prime_UTR_variant MALY-DE 11 47207365 47207365 single base substitution G A intron_variant MALY-DE 11 47207365 47207365 single base substitution G A upstream_gene_variant MALY-DE 11 47208961 47208961 insertion of <=200bp - CCCGGGCGCAGAAGGT upstream_gene_variant MALY-DE 11 47212683 47212683 deletion of <=200bp A - upstream_gene_variant MELA-AU 11 47194216 47194216 single base substitution G A downstream_gene_variant MELA-AU 11 47195152 47195152 single base substitution G A downstream_gene_variant MELA-AU 11 47195286 47195286 single base substitution G A downstream_gene_variant MELA-AU 11 47195516 47195516 single base substitution G A downstream_gene_variant MELA-AU 11 47195870 47195870 single base substitution G A downstream_gene_variant MELA-AU 11 47196360 47196360 single base substitution G A downstream_gene_variant MELA-AU 11 47196915 47196915 single base substitution G A downstream_gene_variant MELA-AU 11 47197486 47197486 single base substitution G A downstream_gene_variant MELA-AU 11 47197683 47197683 single base substitution G A downstream_gene_variant MELA-AU 11 47198299 47198299 single base substitution G A downstream_gene_variant MELA-AU 11 47198561 47198561 single base substitution G A downstream_gene_variant MELA-AU 11 47199260 47199260 single base substitution C T 3_prime_UTR_variant MELA-AU 11 47199260 47199260 single base substitution C T downstream_gene_variant MELA-AU 11 47199674 47199674 single base substitution G A downstream_gene_variant MELA-AU 11 47199674 47199674 single base substitution G A intron_variant MELA-AU 11 47200166 47200166 single base substitution G A downstream_gene_variant MELA-AU 11 47200166 47200166 single base substitution G A intron_variant MELA-AU 11 47200425 47200425 single base substitution G A downstream_gene_variant MELA-AU 11 47200425 47200425 single base substitution G A intron_variant MELA-AU 11 47200459 47200459 single base substitution G A 3_prime_UTR_variant MELA-AU 11 47200459 47200459 single base substitution G A downstream_gene_variant MELA-AU 11 47200459 47200459 single base substitution G A synonymous_variant S341S 1023C>T MELA-AU 11 47200459 47200459 single base substitution G A synonymous_variant S63S 189C>T MELA-AU 11 47200548 47200549 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 47200548 47200549 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 11 47200548 47200549 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant SR311SW MELA-AU 11 47200548 47200549 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant SR33SW MELA-AU 11 47201155 47201155 single base substitution G A downstream_gene_variant MELA-AU 11 47201155 47201155 single base substitution G A intron_variant MELA-AU 11 47201155 47201155 single base substitution G A upstream_gene_variant MELA-AU 11 47201370 47201370 single base substitution G A downstream_gene_variant MELA-AU 11 47201370 47201370 single base substitution G A intron_variant MELA-AU 11 47201370 47201370 single base substitution G A upstream_gene_variant MELA-AU 11 47202044 47202044 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 47202044 47202044 single base substitution G A downstream_gene_variant MELA-AU 11 47202044 47202044 single base substitution G A exon_variant MELA-AU 11 47202044 47202044 single base substitution G A missense_variant R137C 409C>T MELA-AU 11 47202044 47202044 single base substitution G A upstream_gene_variant MELA-AU 11 47202098 47202098 single base substitution G A 5_prime_UTR_variant MELA-AU 11 47202098 47202098 single base substitution G A downstream_gene_variant MELA-AU 11 47202098 47202098 single base substitution G A exon_variant MELA-AU 11 47202098 47202098 single base substitution G A missense_variant H119Y 355C>T MELA-AU 11 47202098 47202098 single base substitution G A upstream_gene_variant MELA-AU 11 47202234 47202234 single base substitution C T 5_prime_UTR_variant MELA-AU 11 47202234 47202234 single base substitution C T downstream_gene_variant MELA-AU 11 47202234 47202234 single base substitution C T exon_variant MELA-AU 11 47202234 47202234 single base substitution C T synonymous_variant Q73Q 219G>A MELA-AU 11 47202234 47202234 single base substitution C T upstream_gene_variant MELA-AU 11 47202716 47202716 single base substitution G A downstream_gene_variant MELA-AU 11 47202716 47202716 single base substitution G A intron_variant MELA-AU 11 47202716 47202716 single base substitution G A upstream_gene_variant MELA-AU 11 47203287 47203287 single base substitution G C downstream_gene_variant MELA-AU 11 47203287 47203287 single base substitution G C intron_variant MELA-AU 11 47203287 47203287 single base substitution G C upstream_gene_variant MELA-AU 11 47203328 47203328 single base substitution G A downstream_gene_variant MELA-AU 11 47203328 47203328 single base substitution G A intron_variant MELA-AU 11 47203328 47203328 single base substitution G A upstream_gene_variant MELA-AU 11 47203939 47203939 single base substitution G A downstream_gene_variant MELA-AU 11 47203939 47203939 single base substitution G A intron_variant MELA-AU 11 47203939 47203939 single base substitution G A upstream_gene_variant MELA-AU 11 47203960 47203960 single base substitution C T 5_prime_UTR_variant MELA-AU 11 47203960 47203960 single base substitution C T exon_variant MELA-AU 11 47203960 47203960 single base substitution C T missense_variant E69K 205G>A MELA-AU 11 47203960 47203960 single base substitution C T upstream_gene_variant MELA-AU 11 47203992 47203992 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 47203992 47203992 single base substitution G A exon_variant MELA-AU 11 47203992 47203992 single base substitution G A missense_variant A58V 173C>T MELA-AU 11 47203992 47203992 single base substitution G A upstream_gene_variant MELA-AU 11 47204247 47204247 single base substitution G A exon_variant MELA-AU 11 47204247 47204247 single base substitution G A intron_variant MELA-AU 11 47204247 47204247 single base substitution G A missense_variant A11V 32C>T MELA-AU 11 47204247 47204247 single base substitution G A upstream_gene_variant MELA-AU 11 47204365 47204365 single base substitution G A intron_variant MELA-AU 11 47204365 47204365 single base substitution G A splice_region_variant MELA-AU 11 47204365 47204365 single base substitution G A upstream_gene_variant MELA-AU 11 47204957 47204957 single base substitution G A intron_variant MELA-AU 11 47204957 47204957 single base substitution G A upstream_gene_variant MELA-AU 11 47205028 47205028 single base substitution G A intron_variant MELA-AU 11 47205028 47205028 single base substitution G A upstream_gene_variant MELA-AU 11 47205213 47205213 single base substitution G A intron_variant MELA-AU 11 47205213 47205213 single base substitution G A upstream_gene_variant MELA-AU 11 47206362 47206362 single base substitution G A intron_variant MELA-AU 11 47206362 47206362 single base substitution G A upstream_gene_variant MELA-AU 11 47206449 47206449 single base substitution G A intron_variant MELA-AU 11 47206449 47206449 single base substitution G A upstream_gene_variant MELA-AU 11 47207195 47207195 single base substitution G A intron_variant MELA-AU 11 47207195 47207195 single base substitution G A splice_region_variant MELA-AU 11 47207195 47207195 single base substitution G A upstream_gene_variant MELA-AU 11 47207383 47207383 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 47207383 47207383 single base substitution T A intron_variant MELA-AU 11 47207383 47207383 single base substitution T A upstream_gene_variant MELA-AU 11 47207819 47207819 single base substitution C T intron_variant MELA-AU 11 47207819 47207819 single base substitution C T upstream_gene_variant MELA-AU 11 47209497 47209501 deletion of <=200bp TTAGG - upstream_gene_variant MELA-AU 11 47211433 47211433 single base substitution C T upstream_gene_variant MELA-AU 11 47212398 47212398 single base substitution A G upstream_gene_variant MELA-AU 11 47212869 47212869 single base substitution C T upstream_gene_variant ORCA-IN 11 47199483 47199483 single base substitution C G 3_prime_UTR_variant ORCA-IN 11 47199483 47199483 single base substitution C G downstream_gene_variant ORCA-IN 11 47199483 47199483 single base substitution C G stop_lost *425S 1274G>C ORCA-IN 11 47202146 47202146 single base substitution G T 5_prime_UTR_variant ORCA-IN 11 47202146 47202146 single base substitution G T downstream_gene_variant ORCA-IN 11 47202146 47202146 single base substitution G T exon_variant ORCA-IN 11 47202146 47202146 single base substitution G T missense_variant Q103K 307C>A ORCA-IN 11 47202146 47202146 single base substitution G T upstream_gene_variant ORCA-IN 11 47211048 47211048 single base substitution C T upstream_gene_variant OV-AU 11 47195031 47195031 single base substitution G T downstream_gene_variant OV-AU 11 47210578 47210578 single base substitution C A upstream_gene_variant PACA-AU 11 47202582 47202582 single base substitution G A downstream_gene_variant PACA-AU 11 47202582 47202582 single base substitution G A intron_variant PACA-AU 11 47202582 47202582 single base substitution G A upstream_gene_variant PACA-AU 11 47203730 47203730 single base substitution A C downstream_gene_variant PACA-AU 11 47203730 47203730 single base substitution A C intron_variant PACA-AU 11 47203730 47203730 single base substitution A C upstream_gene_variant PACA-AU 11 47204294 47204294 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant PACA-AU 11 47204294 47204294 single base substitution C T intron_variant PACA-AU 11 47204294 47204294 single base substitution C T upstream_gene_variant PACA-AU 11 47204638 47204638 single base substitution C T 5_prime_UTR_variant PACA-AU 11 47204638 47204638 single base substitution C T intron_variant PACA-AU 11 47204638 47204638 single base substitution C T upstream_gene_variant PACA-AU 11 47207001 47207001 single base substitution G T intron_variant PACA-AU 11 47207001 47207001 single base substitution G T upstream_gene_variant PACA-AU 11 47208342 47208342 single base substitution C T upstream_gene_variant PACA-CA 11 47194297 47194297 single base substitution C T downstream_gene_variant PACA-CA 11 47199822 47199822 single base substitution G A downstream_gene_variant PACA-CA 11 47199822 47199822 single base substitution G A intron_variant PACA-CA 11 47203707 47203707 single base substitution A G downstream_gene_variant PACA-CA 11 47203707 47203707 single base substitution A G intron_variant PACA-CA 11 47203707 47203707 single base substitution A G upstream_gene_variant PACA-CA 11 47204996 47204996 single base substitution C T intron_variant PACA-CA 11 47204996 47204996 single base substitution C T upstream_gene_variant PACA-CA 11 47206007 47206007 single base substitution C T 5_prime_UTR_variant PACA-CA 11 47206007 47206007 single base substitution C T intron_variant PACA-CA 11 47206007 47206007 single base substitution C T upstream_gene_variant PACA-CA 11 47206459 47206459 single base substitution A G intron_variant PACA-CA 11 47206459 47206459 single base substitution A G upstream_gene_variant PACA-CA 11 47207576 47207576 single base substitution G A intron_variant PACA-CA 11 47207576 47207576 single base substitution G A upstream_gene_variant PACA-CA 11 47211303 47211303 single base substitution T G upstream_gene_variant PAEN-AU 11 47198414 47198414 deletion of <=200bp T - downstream_gene_variant PAEN-AU 11 47201517 47201517 single base substitution A G downstream_gene_variant PAEN-AU 11 47201517 47201517 single base substitution A G intron_variant PAEN-AU 11 47201517 47201517 single base substitution A G upstream_gene_variant PAEN-AU 11 47201982 47201982 single base substitution G A downstream_gene_variant PAEN-AU 11 47201982 47201982 single base substitution G A intron_variant PAEN-AU 11 47201982 47201982 single base substitution G A upstream_gene_variant PAEN-IT 11 47195174 47195174 single base substitution G A downstream_gene_variant PAEN-IT 11 47200817 47200817 single base substitution G A downstream_gene_variant PAEN-IT 11 47200817 47200817 single base substitution G A exon_variant PAEN-IT 11 47200817 47200817 single base substitution G A missense_variant H265Y 793C>T PAEN-IT 11 47200817 47200817 single base substitution G A missense_variant H45Y 133C>T PAEN-IT 11 47200817 47200817 single base substitution G A upstream_gene_variant PAEN-IT 11 47208023 47208023 single base substitution C G upstream_gene_variant PBCA-DE 11 47212692 47212692 single base substitution T A upstream_gene_variant PRAD-CA 11 47195829 47195829 single base substitution T G downstream_gene_variant PRAD-UK 11 47207626 47207626 deletion of <=200bp C - intron_variant PRAD-UK 11 47207626 47207626 deletion of <=200bp C - upstream_gene_variant PRAD-UK 11 47209750 47209750 single base substitution A T upstream_gene_variant PRAD-US 11 47198145 47198145 single base substitution C T downstream_gene_variant RECA-EU 11 47198033 47198033 single base substitution G C downstream_gene_variant RECA-EU 11 47201800 47201800 single base substitution G C 5_prime_UTR_variant RECA-EU 11 47201800 47201800 single base substitution G C downstream_gene_variant RECA-EU 11 47201800 47201800 single base substitution G C exon_variant RECA-EU 11 47201800 47201800 single base substitution G C synonymous_variant V180V 540C>G RECA-EU 11 47201800 47201800 single base substitution G C upstream_gene_variant RECA-EU 11 47203340 47203340 single base substitution C T downstream_gene_variant RECA-EU 11 47203340 47203340 single base substitution C T intron_variant RECA-EU 11 47203340 47203340 single base substitution C T upstream_gene_variant SKCA-BR 11 47194632 47194632 single base substitution A C downstream_gene_variant SKCA-BR 11 47196982 47196982 single base substitution C T downstream_gene_variant SKCA-BR 11 47198415 47198415 single base substitution T C downstream_gene_variant SKCA-BR 11 47198524 47198524 single base substitution T G downstream_gene_variant SKCA-BR 11 47201872 47201872 single base substitution G C 5_prime_UTR_variant SKCA-BR 11 47201872 47201872 single base substitution G C downstream_gene_variant SKCA-BR 11 47201872 47201872 single base substitution G C exon_variant SKCA-BR 11 47201872 47201872 single base substitution G C missense_variant S156R 468C>G SKCA-BR 11 47201872 47201872 single base substitution G C upstream_gene_variant SKCA-BR 11 47204726 47204726 single base substitution G A 5_prime_UTR_variant SKCA-BR 11 47204726 47204726 single base substitution G A intron_variant SKCA-BR 11 47204726 47204726 single base substitution G A upstream_gene_variant SKCA-BR 11 47204783 47204783 single base substitution T G 5_prime_UTR_variant SKCA-BR 11 47204783 47204783 single base substitution T G intron_variant SKCA-BR 11 47204783 47204783 single base substitution T G upstream_gene_variant SKCA-BR 11 47204790 47204790 single base substitution T G 5_prime_UTR_variant SKCA-BR 11 47204790 47204790 single base substitution T G intron_variant SKCA-BR 11 47204790 47204790 single base substitution T G upstream_gene_variant SKCA-BR 11 47207441 47207441 single base substitution T G intron_variant SKCA-BR 11 47207441 47207441 single base substitution T G upstream_gene_variant SKCA-BR 11 47210773 47210773 single base substitution C A upstream_gene_variant SKCA-BR 11 47211470 47211470 single base substitution T C upstream_gene_variant SKCA-BR 11 47211640 47211640 single base substitution C A upstream_gene_variant SKCM-US 11 47200523 47200523 single base substitution G A downstream_gene_variant SKCM-US 11 47200523 47200523 single base substitution G A exon_variant SKCM-US 11 47200523 47200523 single base substitution G A missense_variant P320L 959C>T SKCM-US 11 47200523 47200523 single base substitution G A missense_variant P42L 125C>T SKCM-US 11 47202098 47202098 single base substitution G A 5_prime_UTR_variant SKCM-US 11 47202098 47202098 single base substitution G A downstream_gene_variant SKCM-US 11 47202098 47202098 single base substitution G A exon_variant SKCM-US 11 47202098 47202098 single base substitution G A missense_variant H119Y 355C>T SKCM-US 11 47202098 47202098 single base substitution G A upstream_gene_variant SKCM-US 11 47203992 47203992 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 11 47203992 47203992 single base substitution G A exon_variant SKCM-US 11 47203992 47203992 single base substitution G A missense_variant A58V 173C>T SKCM-US 11 47203992 47203992 single base substitution G A upstream_gene_variant STAD-US 11 47196629 47196629 single base substitution A G downstream_gene_variant STAD-US 11 47196833 47196833 single base substitution G C downstream_gene_variant STAD-US 11 47198097 47198097 single base substitution C T downstream_gene_variant STAD-US 11 47198140 47198140 single base substitution T C downstream_gene_variant STAD-US 11 47202114 47202114 single base substitution C T 5_prime_UTR_variant STAD-US 11 47202114 47202114 single base substitution C T downstream_gene_variant STAD-US 11 47202114 47202114 single base substitution C T exon_variant STAD-US 11 47202114 47202114 single base substitution C T stop_gained W113* 339G>A STAD-US 11 47202114 47202114 single base substitution C T upstream_gene_variant STAD-US 11 47202237 47202237 single base substitution G T 5_prime_UTR_variant STAD-US 11 47202237 47202237 single base substitution G T downstream_gene_variant STAD-US 11 47202237 47202237 single base substitution G T exon_variant STAD-US 11 47202237 47202237 single base substitution G T synonymous_variant P72P 216C>A STAD-US 11 47202237 47202237 single base substitution G T upstream_gene_variant STAD-US 11 47203980 47203980 single base substitution C T 5_prime_UTR_variant STAD-US 11 47203980 47203980 single base substitution C T exon_variant STAD-US 11 47203980 47203980 single base substitution C T missense_variant R62Q 185G>A STAD-US 11 47203980 47203980 single base substitution C T upstream_gene_variant THCA-SA 11 47201769 47201769 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant THCA-SA 11 47201769 47201769 single base substitution G A downstream_gene_variant THCA-SA 11 47201769 47201769 single base substitution G A exon_variant THCA-SA 11 47201769 47201769 single base substitution G A missense_variant R191W 571C>T THCA-SA 11 47201769 47201769 single base substitution G A upstream_gene_variant THCA-US 11 47200728 47200728 single base substitution C A downstream_gene_variant THCA-US 11 47200728 47200728 single base substitution C A exon_variant THCA-US 11 47200728 47200728 single base substitution C A missense_variant M16I 48G>T THCA-US 11 47200728 47200728 single base substitution C A missense_variant M294I 882G>T UCEC-US 11 47199520 47199520 single base substitution G T 3_prime_UTR_variant UCEC-US 11 47199520 47199520 single base substitution G T downstream_gene_variant UCEC-US 11 47199520 47199520 single base substitution G T missense_variant L413M 1237C>A UCEC-US 11 47199528 47199528 single base substitution C A 3_prime_UTR_variant UCEC-US 11 47199528 47199528 single base substitution C A downstream_gene_variant UCEC-US 11 47199528 47199528 single base substitution C A missense_variant R410L 1229G>T UCEC-US 11 47200814 47200814 single base substitution G A downstream_gene_variant UCEC-US 11 47200814 47200814 single base substitution G A exon_variant UCEC-US 11 47200814 47200814 single base substitution G A missense_variant R266C 796C>T UCEC-US 11 47200814 47200814 single base substitution G A missense_variant R46C 136C>T UCEC-US 11 47200814 47200814 single base substitution G A upstream_gene_variant UCEC-US 11 47203980 47203980 single base substitution C T 5_prime_UTR_variant UCEC-US 11 47203980 47203980 single base substitution C T exon_variant UCEC-US 11 47203980 47203980 single base substitution C T missense_variant R62Q 185G>A UCEC-US 11 47203980 47203980 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CHC303T COSM4950493 c.1241A>G p.Y414C Substitution - Missense 11:47177965-47177965 - H1672 COSM313860 c.544C>T p.Q182* Substitution - Nonsense 11:47180245-47180245 - ESO-171 COSM1260810 c.519C>T p.H173H Substitution - coding silent 11:47180270-47180270 - TCGA-GM-A5PV-01 COSM3809300 c.839A>G p.D280G Substitution - Missense 11:47179220-47179220 - T3080 COSM4710799 c.27G>T p.G9G Substitution - coding silent 11:47182701-47182701 - PET100T COSM4963580 c.793C>T p.H265Y Substitution - Missense 11:47179266-47179266 - MD-324 COSM302849 c.389G>T p.R130L Substitution - Missense 11:47180513-47180513 - TCGA-02-2483 COSM2149140 c.263_264delCT p.A88fs*20 Deletion - Frameshift 11:47180638-47180639 - BD188T COSM5500022 c.1226G>A p.G409D Substitution - Missense 11:47177980-47177980 - T2269 COSM4710795 c.918A>C p.T306T Substitution - coding silent 11:47179013-47179013 - TCGA-D7-A4YV-01 COSM4033130 c.216C>A p.P72P Substitution - coding silent 11:47180686-47180686 - CSCC-44-T COSM4457821 c.1061C>A p.S354* Substitution - Nonsense 11:47178464-47178464 - T3024 COSM4710798 c.520G>A p.A174T Substitution - Missense 11:47180269-47180269 - ITNET_0100_T COSM4963580 c.793C>T p.H265Y Substitution - Missense 11:47179266-47179266 - TCGA-AD-6895-01 COSM1354036 c.139G>A p.A47T Substitution - Missense 11:47182475-47182475 - LUAD-F00057 COSM339288 c.103C>T p.L35L Substitution - coding silent 11:47182511-47182511 - sysucc-1370T COSM5469611 c.973C>A p.L325M Substitution - Missense 11:47178958-47178958 - TCGA-AP-A0LT-01 COSM927362 c.1237C>A p.L413M Substitution - Missense 11:47177969-47177969 - TCGA-BH-A0HP-01 COSM3809301 c.634G>A p.E212K Substitution - Missense 11:47179556-47179556 - TCGA-EE-A29L-06 COSM3447753 c.173C>T p.A58V Substitution - Missense 11:47182441-47182441 - TCGA-D1-A176-01 COSM927364 c.796C>T p.R266C Substitution - Missense 11:47179263-47179263 - TCGA-EE-A20C-06 COSM3447752 c.355C>T p.H119Y Substitution - Missense 11:47180547-47180547 - LIM2551 COSM4643544 c.499G>A p.A167T Substitution - Missense 11:47180290-47180290 - T3064 COSM4710796 c.571C>T p.R191W Substitution - Missense 11:47180218-47180218 - TCGA-A6-6780-01 COSM1354035 c.750C>T p.H250H Substitution - coding silent 11:47179440-47179440 - TCGA-C5-A7UC-01 COSM4828112 c.120C>T p.V40V Substitution - coding silent 11:47182494-47182494 - TCGA-EB-A44P-01 COSM3447751 c.959C>T p.P320L Substitution - Missense 11:47178972-47178972 - TCGA-AY-6197-01 COSM1354033 c.1162delG p.E388fs*4 Deletion - Frameshift 11:47178044-47178044 - OSCC-GB_01060111 COSM4883163 c.307C>A p.Q103K Substitution - Missense 11:47180595-47180595 - PTC_435 COSM4710796 c.571C>T p.R191W Substitution - Missense 11:47180218-47180218 - D12 COSM5006869 c.688A>C p.T230P Substitution - Missense 11:47179502-47179502 - CHC1704T COSM4803892 c.404G>C p.G135A Substitution - Missense 11:47180498-47180498 - OSCC-GB_01160111 COSM5956205 c.1274G>C p.*425S Nonstop extension 11:47177932-47177932 - CRC-03T COSM5451140 c.102G>A p.R34R Substitution - coding silent 11:47182512-47182512 - TCGA-BH-A0HP-01 COSM3809302 c.633A>C p.A211A Substitution - coding silent 11:47179557-47179557 - TCGA-CK-4950-01 COSM3752382 c.182C>T p.A61V Substitution - Missense 11:47182432-47182432 - TCGA-BS-A0UT-01 COSM927363 c.1229G>T p.R410L Substitution - Missense 11:47177977-47177977 - ccRCC-25 COSM1663310 c.784C>T p.H262Y Substitution - Missense 11:47179275-47179275 - TCGA-CC-A7II-01 COSM4937641 c.567G>T p.Q189H Substitution - Missense 11:47180222-47180222 - ESCC_35 COSM5628580 c.871G>T p.G291C Substitution - Missense 11:47179188-47179188 - YUPEET COSM1703871 c.1066G>A p.E356K Substitution - Missense 11:47178459-47178459 - HCC63T COSM1604589 c.333C>T p.R111R Substitution - coding silent 11:47180569-47180569 - YUMOBER COSM5372537 c.1000G>A p.G334S Substitution - Missense 11:47178931-47178931 - NB-1977 COSM1286948 c.51G>T p.W17C Substitution - Missense 11:47182677-47182677 - YUKAT COSM5372536 c.1258G>T p.E420* Substitution - Nonsense 11:47177948-47177948 - TCGA-HU-A4GU-01 COSM4033129 c.339G>A p.W113* Substitution - Nonsense 11:47180563-47180563 - B19-Tumor COSM1746267 c.262G>A p.A88T Substitution - Missense 11:47180640-47180640 - CHC303T COSM4950493 c.1241A>G p.Y414C Substitution - Missense 11:47177965-47177965 - Pat_24_A COSM5838638 c.1121A>C p.Y374S Substitution - Missense 11:47178404-47178404 - pfg034T COSM4754421 c.173C>A p.A58D Substitution - Missense 11:47182441-47182441 - C0065T COSM4165797 c.540C>G p.V180V Substitution - coding silent 11:47180249-47180249 - CHEWS034 COSM4574393 c.687G>A p.E229E Substitution - coding silent 11:47179503-47179503 - TCGA-DD-A1EL-01 COSM4926004 c.794A>G p.H265R Substitution - Missense 11:47179265-47179265 - SNU-C2B COSM1981268 c.754C>G p.H252D Substitution - Missense 11:47179436-47179436 - 2171684 COSM4423634 c.548A>T p.E183V Substitution - Missense 11:47180241-47180241 - 2334192 COSM313860 c.544C>T p.Q182* Substitution - Nonsense 11:47180245-47180245 - TCGA-AP-A056-01 COSM927365 c.185G>A p.R62Q Substitution - Missense 11:47182429-47182429 - H1155 COSM1195801 c.68G>A p.R23K Substitution - Missense 11:47182546-47182546 - LUAD_E00623 COSM353744 c.17A>T p.D6V Substitution - Missense 11:47182711-47182711 - T3724 COSM4710797 c.538G>A p.V180I Substitution - Missense 11:47180251-47180251 - TCGA-BP-4760-01 COSM1492512 c.898G>A p.E300K Substitution - Missense 11:47179161-47179161 - PT49 COSM5935777 c.191G>A p.W64* Substitution - Nonsense 11:47182423-47182423 - ESO-887 COSM1260811 c.393G>A p.A131A Substitution - coding silent 11:47180509-47180509 - TCGA-DO-A2HM-01 COSM3368375 c.882G>T p.M294I Substitution - Missense 11:47179177-47179177 - NCI-H716 COSM1981264 c.831C>G p.D277E Substitution - Missense 11:47179228-47179228 - I2L-P7-Tumor-Organoid COSM5361131 c.681C>A p.A227A Substitution - coding silent 11:47179509-47179509 - 10-P1058 COSM4574394 c.94G>A p.G32R Substitution - Missense 11:47182520-47182520 - HCC079T COSM5808117 c.207G>T p.E69D Substitution - Missense 11:47182407-47182407 - LP6005500-DNA_A01 COSM4413765 c.1037+10A>G p.? Unknown 11:47178884-47178884 - PT21_2 COSM5901751 c.212-7C>T p.? Unknown 11:47180697-47180697 - 19M COSM5579231 c.961G>A p.D321N Substitution - Missense 11:47178970-47178970 - BD124T COSM5492794 c.844C>T p.R282C Substitution - Missense 11:47179215-47179215 - CHC1704T COSM4803892 c.404G>C p.G135A Substitution - Missense 11:47180498-47180498 - TCGA-HW-8320-01 COSM3967533 c.261G>A p.A87A Substitution - coding silent 11:47180641-47180641 - TCGA-CG-5721-01 COSM927365 c.185G>A p.R62Q Substitution - Missense 11:47182429-47182429 - TCGA-JW-A5VJ-01 COSM4818485 c.901G>A p.E301K Substitution - Missense 11:47179030-47179030 - TCGA-61-2614-01 COSM1321667 c.656G>A p.R219H Substitution - Missense 11:47179534-47179534 - TCGA-CJ-6027-01 COSM466847 c.423G>T p.K141N Substitution - Missense 11:47180479-47180479 - B19 COSM1746267 c.262G>A p.A88T Substitution - Missense 11:47180640-47180640 - sysucc-1370T COSM5469612 c.854G>A p.R285H Substitution - Missense 11:47179205-47179205 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.334639 11p12-p11.12 606513

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.1-1942T>G 11 47206220 CLL C A Missense p.G32V c.95G>T 11 47204070 LUAD C A Missense p.M294I c.882G>T 11 47200728 THCA C A Missense p.R410L c.1229G>T 11 47199528 UCEC C A Missense p.W17C c.51G>T 11 47204228 NB C T Missense p.E278K c.832G>A 11 47200778 HNSC C T Synonymous p.A131A c.393G>A 11 47202060 ESCA G A 5-UTRSNV . c.1-3087C>T 11 47207365 DLBCL G A Missense p.A58V c.173C>T 11 47203992 CM G A Missense p.H119Y c.355C>T 11 47202098 CM G A Missense p.R266C c.796C>T 11 47200814 UCEC G A Nonsense p.Q182* c.544C>T 11 47201796 SCLC G A Synonymous p.H173H c.519C>T 11 47201821 ESCA G A Synonymous p.H33H c.99C>T 11 47204066 LUAD G A Synonymous p.R48R c.144C>T 11 47204021 STAD G T Missense p.L413M c.1237C>A 11 47199520 UCEC