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 BLCA 11 85956304 85956304 + Silent SNP G G C TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr11:85956304G>C c.33G>C c.(31-33)gcG>gcC p.A11A BLCA 11 85961447 85961447 + Nonsense_Mutation SNP C C G TCGA-DK-A3IT-01A-31D-A20D-08 TCGA-DK-A3IT-10A-01D-A20D-08 g.chr11:85961447C>G c.224C>G c.(223-225)tCa>tGa p.S75* BLCA 11 85977176 85977176 + Missense_Mutation SNP C C T TCGA-FD-A3SO-01A-11D-A22Z-08 TCGA-FD-A3SO-10A-01D-A22Z-08 g.chr11:85977176C>T c.778C>T c.(778-780)Ctt>Ttt p.L260F BLCA 11 85977208 85977208 + Missense_Mutation SNP G G C TCGA-FD-A3SJ-01A-12D-A22Z-08 TCGA-FD-A3SJ-10A-01D-A22Z-08 g.chr11:85977208G>C c.810G>C c.(808-810)atG>atC p.M270I BLCA 11 85977209 85977209 + Missense_Mutation SNP A A T TCGA-FD-A3SJ-01A-12D-A22Z-08 TCGA-FD-A3SJ-10A-01D-A22Z-08 g.chr11:85977209A>T c.811A>T c.(811-813)Atg>Ttg p.M271L BLCA 11 85989563 85989563 + Missense_Mutation SNP G G C TCGA-ZF-A9RL-01A-11D-A38G-08 TCGA-ZF-A9RL-10A-01D-A38J-08 g.chr11:85989563G>C c.1322G>C c.(1321-1323)cGa>cCa p.R441P BRCA 11 85961453 85961453 + Missense_Mutation SNP A A G TCGA-E2-A15E-01A-11D-A12B-09 TCGA-E2-A15E-10A-01D-A12B-09 g.chr11:85961453A>G c.230A>G c.(229-231)aAa>aGa p.K77R BRCA 11 85966327 85966327 + Missense_Mutation SNP G G A TCGA-BH-A1FM-01A-11D-A13L-09 TCGA-BH-A1FM-11B-23D-A188-09 g.chr11:85966327G>A c.424G>A c.(424-426)Gat>Aat p.D142N BRCA 11 85977150 85977150 + Missense_Mutation SNP T T C TCGA-BH-A0W4-01A-11D-A10G-09 TCGA-BH-A0W4-10A-01D-A10G-09 g.chr11:85977150T>C c.752T>C c.(751-753)aTa>aCa p.I251T BRCA 11 85988119 85988119 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:85988119G>A c.1064G>A c.(1063-1065)cGa>cAa p.R355Q COAD 11 85963252 85963252 + Silent SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:85963252A>G c.330A>G c.(328-330)ccA>ccG p.P110P COAD 11 85988174 85988174 + Nonsense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr11:85988174G>A c.1119G>A c.(1117-1119)tgG>tgA p.W373* COAD 11 85989006 85989006 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:85989006T>C c.1172T>C c.(1171-1173)tTa>tCa p.L391S COADREAD 11 85963252 85963252 + Silent SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:85963252A>G c.330A>G c.(328-330)ccA>ccG p.P110P COADREAD 11 85967512 85967512 + Silent SNP C C T TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr11:85967512C>T c.510C>T c.(508-510)ggC>ggT p.G170G COADREAD 11 85988174 85988174 + Nonsense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr11:85988174G>A c.1119G>A c.(1117-1119)tgG>tgA p.W373* COADREAD 11 85989006 85989006 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:85989006T>C c.1172T>C c.(1171-1173)tTa>tCa p.L391S ESCA 11 85961397 85961397 + Missense_Mutation SNP C C G TCGA-L5-A8NS-01A-12D-A37C-09 TCGA-L5-A8NS-11A-11D-A37F-09 g.chr11:85961397C>G c.174C>G c.(172-174)aaC>aaG p.N58K ESCA 11 85966330 85966330 + Splice_Site SNP G G T TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr11:85966330G>T c.e4+1 HNSC 11 85961378 85961378 + Missense_Mutation SNP G G A TCGA-F7-A61V-01A-11D-A28R-08 TCGA-F7-A61V-10A-01D-A28U-08 g.chr11:85961378G>A c.155G>A c.(154-156)cGc>cAc p.R52H HNSC 11 85977185 85977185 + Missense_Mutation SNP T T C TCGA-CN-4741-01A-01D-1434-08 TCGA-CN-4741-10A-01D-1434-08 g.chr11:85977185T>C c.787T>C c.(787-789)Tgg>Cgg p.W263R HNSC 11 85977217 85977217 + Silent SNP A A T TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chr11:85977217A>T c.819A>T c.(817-819)gcA>gcT p.A273A HNSC 11 85979511 85979511 + Nonsense_Mutation SNP C C T TCGA-BA-4077-01B-01D-1434-08 TCGA-BA-4077-10A-01D-1434-08 g.chr11:85979511C>T c.874C>T c.(874-876)Cag>Tag p.Q292* LAML 11 85961447 85961447 + Nonsense_Mutation SNP C C A TCGA-AB-2876-03A-01W-0732-08 TCGA-AB-2876-11A-01W-0732-08 g.chr11:85961447C>A c.224C>A c.(223-225)tCa>tAa p.S75* LAML 11 85968591 85968591 + Missense_Mutation SNP T T A TCGA-AB-3009-03A-01D-0739-09 TCGA-AB-3009-11A-01D-0739-09 g.chr11:85968591T>A c.587T>A c.(586-588)cTg>cAg p.L196Q LIHC 11 85975252 85975260 + In_Frame_Del DEL CTGGTGGCA CTGGTGGCA - TCGA-PD-A5DF-01A-11D-A27I-10 TCGA-PD-A5DF-10A-01D-A27I-10 g.chr11:85975252_85975260delCTGGTGGCA c.673_681delCTGGTGGCA c.(673-681)ctggtggcadel p.LVA225del LIHC 11 85977167 85977167 + Missense_Mutation SNP G G A TCGA-2Y-A9H2-01A-12D-A382-10 TCGA-2Y-A9H2-10A-01D-A385-10 g.chr11:85977167G>A c.769G>A c.(769-771)Gat>Aat p.D257N LUAD 11 85961365 85961365 + Missense_Mutation SNP A A G TCGA-91-6835-01A-11D-1855-08 TCGA-91-6835-11A-01D-1855-08 g.chr11:85961365A>G c.142A>G c.(142-144)Aca>Gca p.T48A LUAD 11 85963272 85963272 + Missense_Mutation SNP G G T TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr11:85963272G>T c.350G>T c.(349-351)gGa>gTa p.G117V LUAD 11 85967511 85967511 + Missense_Mutation SNP G G T TCGA-97-7938-01A-11D-2167-08 TCGA-97-7938-10A-01D-2167-08 g.chr11:85967511G>T c.509G>T c.(508-510)gGc>gTc p.G170V LUAD 11 85975297 85975297 + Missense_Mutation SNP C C G TCGA-86-8056-01A-11D-2238-08 TCGA-86-8056-10A-01D-2238-08 g.chr11:85975297C>G c.718C>G c.(718-720)Cta>Gta p.L240V LUAD 11 85979592 85979592 + Missense_Mutation SNP A A C TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr11:85979592A>C c.955A>C c.(955-957)Ata>Cta p.I319L LUAD 11 85979601 85979601 + Missense_Mutation SNP A A G TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr11:85979601A>G c.964A>G c.(964-966)Aag>Gag p.K322E LUAD 11 85988962 85988962 + Missense_Mutation SNP G G T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr11:85988962G>T c.1128G>T c.(1126-1128)atG>atT p.M376I LUAD 11 85989472 85989472 + Missense_Mutation SNP G G C TCGA-69-7765-01A-11D-2167-08 TCGA-69-7765-10A-01D-2167-08 g.chr11:85989472G>C c.1231G>C c.(1231-1233)Gct>Cct p.A411P LUSC 11 85977186 85977186 + Missense_Mutation SNP G G T TCGA-18-3410-01A-01D-0983-08 TCGA-18-3410-11A-01D-0983-08 g.chr11:85977186G>T c.788G>T c.(787-789)tGg>tTg p.W263L LUSC 11 85988171 85988171 + Missense_Mutation SNP C C A TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr11:85988171C>A c.1116C>A c.(1114-1116)ttC>ttA p.F372L PAAD 11 85967452 85967452 + Silent SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:85967452T>C c.450T>C c.(448-450)tgT>tgC p.C150C PAAD 11 85988058 85988058 + Missense_Mutation SNP A A C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:85988058A>C c.1003A>C c.(1003-1005)Aag>Cag p.K335Q PAAD 11 85988142 85988142 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:85988142A>G c.1087A>G c.(1087-1089)Att>Gtt p.I363V PRAD 11 85968564 85968564 + Missense_Mutation SNP T T G TCGA-EJ-5524-01A-01D-1576-08 TCGA-EJ-5524-10A-01D-1577-08 g.chr11:85968564T>G c.560T>G c.(559-561)gTt>gGt p.V187G PRAD 11 85988974 85988974 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:85988974C>T c.1140C>T c.(1138-1140)ggC>ggT p.G380G READ 11 85967512 85967512 + Silent SNP C C T TCGA-CI-6624-01C-11D-1826-10 TCGA-CI-6624-10A-01D-1826-10 g.chr11:85967512C>T c.510C>T c.(508-510)ggC>ggT p.G170G SARC 11 85977214 85977214 + Frame_Shift_Del DEL T T - TCGA-DX-AB30-01A-11D-A38Z-09 TCGA-DX-AB30-10A-01D-A38Z-09 g.chr11:85977214delT c.816delT c.(814-816)aatfs p.N272fs SKCM 11 85963196 85963196 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr11:85963196C>T c.274C>T c.(274-276)Cat>Tat p.H92Y SKCM 11 85967484 85967484 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:85967484C>T c.482C>T c.(481-483)cCt>cTt p.P161L SKCM 11 85989562 85989562 + Nonsense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:85989562C>T c.1321C>T c.(1321-1323)Cga>Tga p.R441*

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 85967486 85967486 single base substitution C T exon_variant BLCA-CN 11 85967486 85967486 single base substitution C T intron_variant BLCA-CN 11 85967486 85967486 single base substitution C T synonymous_variant L162L 484C>T BLCA-CN 11 85968628 85968628 single base substitution A C exon_variant BLCA-CN 11 85968628 85968628 single base substitution A C intron_variant BLCA-CN 11 85968628 85968628 single base substitution A C synonymous_variant S208S 624A>C BLCA-US 11 85961447 85961447 single base substitution C G exon_variant BLCA-US 11 85961447 85961447 single base substitution C G intron_variant BLCA-US 11 85961447 85961447 single base substitution C G stop_gained S75* 224C>G BLCA-US 11 85977176 85977176 single base substitution C T exon_variant BLCA-US 11 85977176 85977176 single base substitution C T intron_variant BLCA-US 11 85977176 85977176 single base substitution C T missense_variant L260F 778C>T BLCA-US 11 85977176 85977176 single base substitution C T upstream_gene_variant BOCA-FR 11 85954820 85954820 single base substitution G A upstream_gene_variant BRCA-EU 11 85952766 85952766 single base substitution C G upstream_gene_variant BRCA-EU 11 85953060 85953060 single base substitution C A upstream_gene_variant BRCA-EU 11 85953400 85953400 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 85954942 85954942 single base substitution G A upstream_gene_variant BRCA-EU 11 85955687 85955687 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 11 85955687 85955687 single base substitution A T upstream_gene_variant BRCA-EU 11 85956696 85956696 single base substitution G C intron_variant BRCA-EU 11 85957610 85957610 single base substitution G T intron_variant BRCA-EU 11 85958668 85958668 deletion of <=200bp T - intron_variant BRCA-EU 11 85958795 85958795 single base substitution T C intron_variant BRCA-EU 11 85958817 85958817 single base substitution A C intron_variant BRCA-EU 11 85959210 85959210 single base substitution G A intron_variant BRCA-EU 11 85962356 85962356 single base substitution T C intron_variant BRCA-EU 11 85962381 85962381 single base substitution C T intron_variant BRCA-EU 11 85963557 85963557 insertion of <=200bp - CT intron_variant BRCA-EU 11 85963751 85963751 deletion of <=200bp T - intron_variant BRCA-EU 11 85971230 85971230 single base substitution C T intron_variant BRCA-EU 11 85971230 85971230 single base substitution C T upstream_gene_variant BRCA-EU 11 85971488 85971488 single base substitution C G intron_variant BRCA-EU 11 85971488 85971488 single base substitution C G upstream_gene_variant BRCA-EU 11 85972831 85972831 single base substitution A T intron_variant BRCA-EU 11 85972831 85972831 single base substitution A T upstream_gene_variant BRCA-EU 11 85973099 85973099 insertion of <=200bp - T intron_variant BRCA-EU 11 85973099 85973099 insertion of <=200bp - T upstream_gene_variant BRCA-EU 11 85979728 85979728 single base substitution T C downstream_gene_variant BRCA-EU 11 85979728 85979728 single base substitution T C intron_variant BRCA-EU 11 85979747 85979747 deletion of <=200bp T - downstream_gene_variant BRCA-EU 11 85979747 85979747 deletion of <=200bp T - intron_variant BRCA-EU 11 85982725 85982725 single base substitution G A downstream_gene_variant BRCA-EU 11 85982725 85982725 single base substitution G A intron_variant BRCA-EU 11 85982725 85982725 single base substitution G A upstream_gene_variant BRCA-EU 11 85983865 85983866 deletion of <=200bp TT - downstream_gene_variant BRCA-EU 11 85983865 85983866 deletion of <=200bp TT - intron_variant BRCA-EU 11 85983865 85983866 deletion of <=200bp TT - upstream_gene_variant BRCA-EU 11 85985842 85985842 single base substitution C T intron_variant BRCA-EU 11 85985842 85985842 single base substitution C T upstream_gene_variant BRCA-EU 11 85987222 85987222 single base substitution T G 5_prime_UTR_variant BRCA-EU 11 85987222 85987222 single base substitution T G intron_variant BRCA-EU 11 85987222 85987222 single base substitution T G upstream_gene_variant BRCA-EU 11 85988537 85988537 single base substitution C T exon_variant BRCA-EU 11 85988537 85988537 single base substitution C T intron_variant BRCA-EU 11 85989366 85989366 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 85989366 85989366 single base substitution C G downstream_gene_variant BRCA-EU 11 85989366 85989366 single base substitution C G intron_variant BRCA-EU 11 85990389 85990389 single base substitution T A downstream_gene_variant BRCA-EU 11 85990907 85990907 single base substitution G A downstream_gene_variant BRCA-EU 11 85992243 85992243 single base substitution C G downstream_gene_variant BRCA-EU 11 85994517 85994517 single base substitution G C downstream_gene_variant BRCA-FR 11 85954942 85954942 single base substitution G A upstream_gene_variant BRCA-FR 11 85956696 85956696 single base substitution G C intron_variant BRCA-FR 11 85978607 85978607 single base substitution G A intron_variant BRCA-FR 11 85978607 85978607 single base substitution G A upstream_gene_variant BRCA-FR 11 85989366 85989366 single base substitution C G 3_prime_UTR_variant BRCA-FR 11 85989366 85989366 single base substitution C G downstream_gene_variant BRCA-FR 11 85989366 85989366 single base substitution C G intron_variant BRCA-US 11 85961453 85961453 single base substitution A G exon_variant BRCA-US 11 85961453 85961453 single base substitution A G intron_variant BRCA-US 11 85961453 85961453 single base substitution A G missense_variant K77R 230A>G BRCA-US 11 85966327 85966327 single base substitution G A intron_variant BRCA-US 11 85966327 85966327 single base substitution G A missense_variant D142N 424G>A BRCA-US 11 85966327 85966327 single base substitution G A splice_region_variant BRCA-US 11 85977150 85977150 single base substitution T C exon_variant BRCA-US 11 85977150 85977150 single base substitution T C intron_variant BRCA-US 11 85977150 85977150 single base substitution T C missense_variant I251T 752T>C BRCA-US 11 85977150 85977150 single base substitution T C upstream_gene_variant BRCA-US 11 85988119 85988119 single base substitution G A exon_variant BRCA-US 11 85988119 85988119 single base substitution G A missense_variant R20Q 59G>A BRCA-US 11 85988119 85988119 single base substitution G A missense_variant R275Q 824G>A BRCA-US 11 85988119 85988119 single base substitution G A missense_variant R355Q 1064G>A BRCA-US 11 85988119 85988119 single base substitution G A missense_variant R380Q 1139G>A BRCA-US 11 85988119 85988119 single base substitution G A missense_variant R69Q 206G>A BRCA-US 11 85988119 85988119 single base substitution G A upstream_gene_variant BTCA-JP 11 85968623 85968623 single base substitution C T exon_variant BTCA-JP 11 85968623 85968623 single base substitution C T intron_variant BTCA-JP 11 85968623 85968623 single base substitution C T synonymous_variant L207L 619C>T BTCA-JP 11 85968691 85968691 single base substitution G T intron_variant BTCA-JP 11 85979669 85979669 single base substitution A G downstream_gene_variant BTCA-JP 11 85979669 85979669 single base substitution A G intron_variant BTCA-JP 11 85979675 85979675 single base substitution G A downstream_gene_variant BTCA-JP 11 85979675 85979675 single base substitution G A intron_variant CLLE-ES 11 85960845 85960845 single base substitution G A intron_variant CLLE-ES 11 85961308 85961308 single base substitution A G intron_variant CLLE-ES 11 85964767 85964767 single base substitution T A intron_variant CLLE-ES 11 85978382 85978382 single base substitution T G intron_variant CLLE-ES 11 85978382 85978382 single base substitution T G upstream_gene_variant CLLE-ES 11 85990204 85990204 single base substitution A G downstream_gene_variant COCA-CN 11 85963555 85963555 single base substitution C T intron_variant COCA-CN 11 85979669 85979669 single base substitution A G downstream_gene_variant COCA-CN 11 85979669 85979669 single base substitution A G intron_variant COCA-CN 11 85988942 85988942 single base substitution A T downstream_gene_variant COCA-CN 11 85988942 85988942 single base substitution A T exon_variant COCA-CN 11 85988942 85988942 single base substitution A T intron_variant EOPC-DE 11 85963557 85963557 single base substitution T C intron_variant EOPC-DE 11 85993946 85993946 single base substitution C A downstream_gene_variant ESAD-UK 11 85951966 85951966 single base substitution C T upstream_gene_variant ESAD-UK 11 85952371 85952371 single base substitution G T upstream_gene_variant ESAD-UK 11 85953045 85953045 single base substitution C G upstream_gene_variant ESAD-UK 11 85954928 85954928 deletion of <=200bp A - upstream_gene_variant ESAD-UK 11 85955451 85955451 single base substitution G A upstream_gene_variant ESAD-UK 11 85957161 85957161 single base substitution T A intron_variant ESAD-UK 11 85959303 85959303 single base substitution G A intron_variant ESAD-UK 11 85959788 85959788 single base substitution C T intron_variant ESAD-UK 11 85960223 85960223 single base substitution T C intron_variant ESAD-UK 11 85961344 85961344 single base substitution G A exon_variant ESAD-UK 11 85961344 85961344 single base substitution G A intron_variant ESAD-UK 11 85961344 85961344 single base substitution G A missense_variant A41T 121G>A ESAD-UK 11 85961457 85961457 single base substitution C T exon_variant ESAD-UK 11 85961457 85961457 single base substitution C T intron_variant ESAD-UK 11 85961457 85961457 single base substitution C T synonymous_variant C78C 234C>T ESAD-UK 11 85961499 85961499 deletion of <=200bp A - intron_variant ESAD-UK 11 85966297 85966297 single base substitution A C exon_variant ESAD-UK 11 85966297 85966297 single base substitution A C intron_variant ESAD-UK 11 85966297 85966297 single base substitution A C missense_variant I132L 394A>C ESAD-UK 11 85967358 85967358 single base substitution A C intron_variant ESAD-UK 11 85967388 85967388 single base substitution T A intron_variant ESAD-UK 11 85967774 85967774 single base substitution T C intron_variant ESAD-UK 11 85969724 85969724 single base substitution A G intron_variant ESAD-UK 11 85969827 85969827 single base substitution A G intron_variant ESAD-UK 11 85970076 85970076 deletion of <=200bp T - intron_variant ESAD-UK 11 85970076 85970076 deletion of <=200bp T - upstream_gene_variant ESAD-UK 11 85971126 85971126 single base substitution A C intron_variant ESAD-UK 11 85971126 85971126 single base substitution A C upstream_gene_variant ESAD-UK 11 85971227 85971227 single base substitution T C intron_variant ESAD-UK 11 85971227 85971227 single base substitution T C upstream_gene_variant ESAD-UK 11 85973544 85973544 single base substitution C T intron_variant ESAD-UK 11 85973544 85973544 single base substitution C T upstream_gene_variant ESAD-UK 11 85974597 85974597 single base substitution A T intron_variant ESAD-UK 11 85974597 85974597 single base substitution A T upstream_gene_variant ESAD-UK 11 85975610 85975610 single base substitution G A exon_variant ESAD-UK 11 85975610 85975610 single base substitution G A intron_variant ESAD-UK 11 85975610 85975610 single base substitution G A upstream_gene_variant ESAD-UK 11 85978263 85978263 single base substitution A G intron_variant ESAD-UK 11 85978263 85978263 single base substitution A G upstream_gene_variant ESAD-UK 11 85979464 85979464 single base substitution C T exon_variant ESAD-UK 11 85979464 85979464 single base substitution C T intron_variant ESAD-UK 11 85980074 85980074 single base substitution G A downstream_gene_variant ESAD-UK 11 85980074 85980074 single base substitution G A intron_variant ESAD-UK 11 85981470 85981470 single base substitution C T downstream_gene_variant ESAD-UK 11 85981470 85981470 single base substitution C T intron_variant ESAD-UK 11 85984924 85984924 single base substitution G C intron_variant ESAD-UK 11 85984924 85984924 single base substitution G C upstream_gene_variant ESAD-UK 11 85984929 85984929 single base substitution C T intron_variant ESAD-UK 11 85984929 85984929 single base substitution C T upstream_gene_variant ESAD-UK 11 85987739 85987739 single base substitution T C 5_prime_UTR_variant ESAD-UK 11 85987739 85987739 single base substitution T C intron_variant ESAD-UK 11 85987739 85987739 single base substitution T C upstream_gene_variant ESAD-UK 11 85989812 85989812 deletion of <=200bp A - 3_prime_UTR_variant ESAD-UK 11 85989812 85989812 deletion of <=200bp A - downstream_gene_variant ESAD-UK 11 85992391 85992391 single base substitution T G downstream_gene_variant ESAD-UK 11 85992451 85992451 deletion of <=200bp T - downstream_gene_variant ESAD-UK 11 85992986 85992986 single base substitution C T downstream_gene_variant ESAD-UK 11 85993791 85993791 single base substitution G A downstream_gene_variant ESAD-UK 11 85994575 85994575 single base substitution G A downstream_gene_variant ESAD-UK 11 85994789 85994789 deletion of <=200bp T - downstream_gene_variant ESCA-CN 11 85979637 85979638 deletion of <=200bp GT - downstream_gene_variant ESCA-CN 11 85979637 85979638 deletion of <=200bp GT - intron_variant KIRP-US 11 85956385 85956385 single base substitution T A missense_variant N36K 108T>A KIRP-US 11 85956385 85956385 single base substitution T A missense_variant N38K 114T>A KIRP-US 11 85956385 85956385 single base substitution T A splice_region_variant LAML-KR 11 85961434 85961434 single base substitution G T exon_variant LAML-KR 11 85961434 85961434 single base substitution G T intron_variant LAML-KR 11 85961434 85961434 single base substitution G T stop_gained G71* 211G>T LAML-KR 11 85968739 85968739 single base substitution A G intron_variant LAML-KR 11 85979669 85979669 single base substitution A G downstream_gene_variant LAML-KR 11 85979669 85979669 single base substitution A G intron_variant LICA-FR 11 85967549 85967549 single base substitution A G exon_variant LICA-FR 11 85967549 85967549 single base substitution A G intron_variant LICA-FR 11 85967549 85967549 single base substitution A G missense_variant I183V 547A>G LICA-FR 11 85968383 85968384 deletion of <=200bp TT - intron_variant LICA-FR 11 85973856 85973856 deletion of <=200bp T - intron_variant LICA-FR 11 85973856 85973856 deletion of <=200bp T - upstream_gene_variant LIHC-US 11 85975252 85975260 deletion of <=200bp CTGGTGGCA - exon_variant LIHC-US 11 85975252 85975260 deletion of <=200bp CTGGTGGCA - inframe_deletion LVA225 LIHC-US 11 85975252 85975260 deletion of <=200bp CTGGTGGCA - intron_variant LIHC-US 11 85975252 85975260 deletion of <=200bp CTGGTGGCA - upstream_gene_variant LIHC-US 11 85975264 85975264 single base substitution T G exon_variant LIHC-US 11 85975264 85975264 single base substitution T G intron_variant LIHC-US 11 85975264 85975264 single base substitution T G missense_variant F229V 685T>G LIHC-US 11 85975264 85975264 single base substitution T G upstream_gene_variant LINC-JP 11 85956218 85956218 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 11 85956218 85956218 single base substitution G C upstream_gene_variant LINC-JP 11 85989383 85989383 single base substitution G T 3_prime_UTR_variant LINC-JP 11 85989383 85989383 single base substitution G T downstream_gene_variant LINC-JP 11 85989383 85989383 single base substitution G T intron_variant LINC-JP 11 85993395 85993395 single base substitution A G downstream_gene_variant LIRI-JP 11 85951861 85951861 single base substitution C T upstream_gene_variant LIRI-JP 11 85954527 85954527 single base substitution G T upstream_gene_variant LIRI-JP 11 85956571 85956571 single base substitution G A intron_variant LIRI-JP 11 85960303 85960303 single base substitution C T intron_variant LIRI-JP 11 85960816 85960816 single base substitution C G intron_variant LIRI-JP 11 85961094 85961094 single base substitution A G intron_variant LIRI-JP 11 85962120 85962120 single base substitution T A intron_variant LIRI-JP 11 85967472 85967472 single base substitution A G exon_variant LIRI-JP 11 85967472 85967472 single base substitution A G intron_variant LIRI-JP 11 85967472 85967472 single base substitution A G missense_variant N157S 470A>G LIRI-JP 11 85971699 85971699 single base substitution C G intron_variant LIRI-JP 11 85971699 85971699 single base substitution C G upstream_gene_variant LIRI-JP 11 85973589 85973589 single base substitution C T intron_variant LIRI-JP 11 85973589 85973589 single base substitution C T upstream_gene_variant LIRI-JP 11 85975627 85975627 single base substitution A G exon_variant LIRI-JP 11 85975627 85975627 single base substitution A G intron_variant LIRI-JP 11 85975627 85975627 single base substitution A G upstream_gene_variant LIRI-JP 11 85975711 85975711 single base substitution T C exon_variant LIRI-JP 11 85975711 85975711 single base substitution T C intron_variant LIRI-JP 11 85975711 85975711 single base substitution T C upstream_gene_variant LIRI-JP 11 85977290 85977290 single base substitution A G intron_variant LIRI-JP 11 85977290 85977290 single base substitution A G upstream_gene_variant LIRI-JP 11 85977828 85977828 single base substitution A G intron_variant LIRI-JP 11 85977828 85977828 single base substitution A G upstream_gene_variant LIRI-JP 11 85978157 85978157 single base substitution A G intron_variant LIRI-JP 11 85978157 85978157 single base substitution A G upstream_gene_variant LIRI-JP 11 85978432 85978432 single base substitution A C intron_variant LIRI-JP 11 85978432 85978432 single base substitution A C upstream_gene_variant LIRI-JP 11 85978452 85978452 single base substitution A G intron_variant LIRI-JP 11 85978452 85978452 single base substitution A G upstream_gene_variant LIRI-JP 11 85979606 85979606 single base substitution A G downstream_gene_variant LIRI-JP 11 85979606 85979606 single base substitution A G intron_variant LIRI-JP 11 85979606 85979606 single base substitution A G splice_region_variant LIRI-JP 11 85982032 85982032 single base substitution A G downstream_gene_variant LIRI-JP 11 85982032 85982032 single base substitution A G intron_variant LIRI-JP 11 85984925 85984925 single base substitution A G intron_variant LIRI-JP 11 85984925 85984925 single base substitution A G upstream_gene_variant LIRI-JP 11 85986963 85986963 single base substitution A G intron_variant LIRI-JP 11 85986963 85986963 single base substitution A G upstream_gene_variant LIRI-JP 11 85987386 85987386 single base substitution C T 5_prime_UTR_variant LIRI-JP 11 85987386 85987386 single base substitution C T intron_variant LIRI-JP 11 85987386 85987386 single base substitution C T upstream_gene_variant LIRI-JP 11 85987393 85987393 single base substitution A T 5_prime_UTR_variant LIRI-JP 11 85987393 85987393 single base substitution A T intron_variant LIRI-JP 11 85987393 85987393 single base substitution A T upstream_gene_variant LIRI-JP 11 85989242 85989242 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 85989242 85989242 single base substitution A G downstream_gene_variant LIRI-JP 11 85989242 85989242 single base substitution A G intron_variant LIRI-JP 11 85992191 85992191 single base substitution A G downstream_gene_variant LIRI-JP 11 85992922 85992922 single base substitution A G downstream_gene_variant LUSC-KR 11 85952749 85952749 single base substitution C G upstream_gene_variant LUSC-KR 11 85954881 85954881 single base substitution C T upstream_gene_variant LUSC-KR 11 85956908 85956908 single base substitution C G intron_variant LUSC-KR 11 85961166 85961166 single base substitution C T intron_variant LUSC-KR 11 85963092 85963092 single base substitution A G intron_variant LUSC-KR 11 85963630 85963630 single base substitution G T intron_variant LUSC-KR 11 85965013 85965013 single base substitution C T intron_variant LUSC-KR 11 85968623 85968623 single base substitution C T exon_variant LUSC-KR 11 85968623 85968623 single base substitution C T intron_variant LUSC-KR 11 85968623 85968623 single base substitution C T synonymous_variant L207L 619C>T LUSC-KR 11 85969615 85969615 single base substitution G T intron_variant LUSC-KR 11 85992640 85992640 single base substitution A G downstream_gene_variant LUSC-US 11 85977186 85977186 single base substitution G T exon_variant LUSC-US 11 85977186 85977186 single base substitution G T intron_variant LUSC-US 11 85977186 85977186 single base substitution G T missense_variant W263L 788G>T LUSC-US 11 85977186 85977186 single base substitution G T upstream_gene_variant LUSC-US 11 85988171 85988171 single base substitution C A exon_variant LUSC-US 11 85988171 85988171 single base substitution C A missense_variant F292L 876C>A LUSC-US 11 85988171 85988171 single base substitution C A missense_variant F372L 1116C>A LUSC-US 11 85988171 85988171 single base substitution C A missense_variant F37L 111C>A LUSC-US 11 85988171 85988171 single base substitution C A missense_variant F397L 1191C>A LUSC-US 11 85988171 85988171 single base substitution C A missense_variant F86L 258C>A MALY-DE 11 85952569 85952572 deletion of <=200bp ATGA - upstream_gene_variant MALY-DE 11 85958525 85958525 single base substitution A G intron_variant MALY-DE 11 85958967 85958967 single base substitution G A intron_variant MALY-DE 11 85959016 85959016 single base substitution A G intron_variant MALY-DE 11 85962368 85962368 single base substitution T G intron_variant MALY-DE 11 85962383 85962383 single base substitution T A intron_variant MALY-DE 11 85962401 85962401 single base substitution T A intron_variant MALY-DE 11 85963557 85963557 single base substitution T C intron_variant MALY-DE 11 85973268 85973268 deletion of <=200bp T - intron_variant MALY-DE 11 85973268 85973268 deletion of <=200bp T - upstream_gene_variant MALY-DE 11 85979558 85979558 single base substitution T C exon_variant MALY-DE 11 85979558 85979558 single base substitution T C intron_variant MALY-DE 11 85979558 85979558 single base substitution T C synonymous_variant N307N 921T>C MALY-DE 11 85984769 85984769 single base substitution C T intron_variant MALY-DE 11 85984769 85984769 single base substitution C T upstream_gene_variant MALY-DE 11 85991992 85991992 single base substitution T C downstream_gene_variant MALY-DE 11 85994784 85994784 single base substitution A G downstream_gene_variant MELA-AU 11 85950703 85950703 single base substitution G A upstream_gene_variant MELA-AU 11 85950824 85950824 single base substitution T A upstream_gene_variant MELA-AU 11 85950973 85950973 single base substitution G A upstream_gene_variant MELA-AU 11 85950997 85950997 single base substitution G A upstream_gene_variant MELA-AU 11 85952248 85952248 single base substitution C T upstream_gene_variant MELA-AU 11 85952396 85952398 deletion of <=200bp TTA - upstream_gene_variant MELA-AU 11 85952444 85952444 single base substitution C T upstream_gene_variant MELA-AU 11 85953505 85953505 single base substitution C T upstream_gene_variant MELA-AU 11 85953537 85953537 single base substitution T C upstream_gene_variant MELA-AU 11 85953807 85953807 single base substitution C T upstream_gene_variant MELA-AU 11 85953814 85953814 single base substitution C T upstream_gene_variant MELA-AU 11 85953916 85953916 single base substitution C T upstream_gene_variant MELA-AU 11 85954091 85954092 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 85954332 85954332 single base substitution C T upstream_gene_variant MELA-AU 11 85954346 85954346 single base substitution G A upstream_gene_variant MELA-AU 11 85954530 85954530 single base substitution C T upstream_gene_variant MELA-AU 11 85954550 85954550 single base substitution G A upstream_gene_variant MELA-AU 11 85955515 85955515 single base substitution G A upstream_gene_variant MELA-AU 11 85955584 85955584 single base substitution C T upstream_gene_variant MELA-AU 11 85955794 85955794 single base substitution C T 5_prime_UTR_variant MELA-AU 11 85955794 85955794 single base substitution C T upstream_gene_variant MELA-AU 11 85956237 85956237 single base substitution C T 5_prime_UTR_variant MELA-AU 11 85956237 85956237 single base substitution C T upstream_gene_variant MELA-AU 11 85956276 85956276 single base substitution C T 5_prime_UTR_variant MELA-AU 11 85956276 85956276 single base substitution C T missense_variant S2F 5C>T MELA-AU 11 85956276 85956276 single base substitution C T upstream_gene_variant MELA-AU 11 85956589 85956589 single base substitution G A intron_variant MELA-AU 11 85959214 85959214 single base substitution G A intron_variant MELA-AU 11 85960890 85960890 single base substitution T G intron_variant MELA-AU 11 85963174 85963174 single base substitution C T intron_variant MELA-AU 11 85963214 85963214 single base substitution G A exon_variant MELA-AU 11 85963214 85963214 single base substitution G A intron_variant MELA-AU 11 85963214 85963214 single base substitution G A missense_variant G98R 292G>A MELA-AU 11 85963903 85963903 single base substitution G A intron_variant MELA-AU 11 85963997 85963997 single base substitution C T intron_variant MELA-AU 11 85964871 85964871 single base substitution C T intron_variant MELA-AU 11 85965488 85965488 single base substitution G A intron_variant MELA-AU 11 85965596 85965596 single base substitution C T intron_variant MELA-AU 11 85966265 85966265 single base substitution T C intron_variant MELA-AU 11 85966265 85966265 single base substitution T C missense_variant V121A 362T>C MELA-AU 11 85966265 85966265 single base substitution T C splice_region_variant MELA-AU 11 85966415 85966415 single base substitution C T intron_variant MELA-AU 11 85968740 85968740 single base substitution G A intron_variant MELA-AU 11 85968939 85968939 single base substitution C T intron_variant MELA-AU 11 85969244 85969244 single base substitution C T intron_variant MELA-AU 11 85969375 85969376 multiple base substitution (>=2bp and <=200bp) CT TA intron_variant MELA-AU 11 85969607 85969607 single base substitution T A intron_variant MELA-AU 11 85971250 85971250 single base substitution T C intron_variant MELA-AU 11 85971250 85971250 single base substitution T C upstream_gene_variant MELA-AU 11 85971445 85971445 single base substitution A T intron_variant MELA-AU 11 85971445 85971445 single base substitution A T upstream_gene_variant MELA-AU 11 85971813 85971813 single base substitution C T intron_variant MELA-AU 11 85971813 85971813 single base substitution C T upstream_gene_variant MELA-AU 11 85972192 85972192 single base substitution T A intron_variant MELA-AU 11 85972192 85972192 single base substitution T A upstream_gene_variant MELA-AU 11 85972196 85972196 single base substitution C T intron_variant MELA-AU 11 85972196 85972196 single base substitution C T upstream_gene_variant MELA-AU 11 85972358 85972358 single base substitution C T intron_variant MELA-AU 11 85972358 85972358 single base substitution C T upstream_gene_variant MELA-AU 11 85972580 85972580 single base substitution C G intron_variant MELA-AU 11 85972580 85972580 single base substitution C G upstream_gene_variant MELA-AU 11 85972677 85972677 single base substitution C T intron_variant MELA-AU 11 85972677 85972677 single base substitution C T upstream_gene_variant MELA-AU 11 85972707 85972707 single base substitution C T intron_variant MELA-AU 11 85972707 85972707 single base substitution C T upstream_gene_variant MELA-AU 11 85973304 85973304 single base substitution C T intron_variant MELA-AU 11 85973304 85973304 single base substitution C T upstream_gene_variant MELA-AU 11 85973383 85973383 single base substitution T G intron_variant MELA-AU 11 85973383 85973383 single base substitution T G upstream_gene_variant MELA-AU 11 85975360 85975360 single base substitution C T exon_variant MELA-AU 11 85975360 85975360 single base substitution C T intron_variant MELA-AU 11 85975360 85975360 single base substitution C T upstream_gene_variant MELA-AU 11 85975754 85975754 single base substitution C T exon_variant MELA-AU 11 85975754 85975754 single base substitution C T intron_variant MELA-AU 11 85975754 85975754 single base substitution C T upstream_gene_variant MELA-AU 11 85976348 85976348 single base substitution C T exon_variant MELA-AU 11 85976348 85976348 single base substitution C T intron_variant MELA-AU 11 85976348 85976348 single base substitution C T upstream_gene_variant MELA-AU 11 85976895 85976895 single base substitution C T exon_variant MELA-AU 11 85976895 85976895 single base substitution C T intron_variant MELA-AU 11 85976895 85976895 single base substitution C T upstream_gene_variant MELA-AU 11 85977422 85977422 single base substitution C T intron_variant MELA-AU 11 85977422 85977422 single base substitution C T upstream_gene_variant MELA-AU 11 85977959 85977959 single base substitution G A intron_variant MELA-AU 11 85977959 85977959 single base substitution G A upstream_gene_variant MELA-AU 11 85978331 85978331 single base substitution C T intron_variant MELA-AU 11 85978331 85978331 single base substitution C T upstream_gene_variant MELA-AU 11 85978362 85978362 single base substitution T G intron_variant MELA-AU 11 85978362 85978362 single base substitution T G upstream_gene_variant MELA-AU 11 85978653 85978653 single base substitution T G intron_variant MELA-AU 11 85978653 85978653 single base substitution T G upstream_gene_variant MELA-AU 11 85979269 85979269 single base substitution C T exon_variant MELA-AU 11 85979269 85979269 single base substitution C T intron_variant MELA-AU 11 85979491 85979491 single base substitution C T exon_variant MELA-AU 11 85979491 85979491 single base substitution C T intron_variant MELA-AU 11 85979491 85979491 single base substitution C T splice_region_variant MELA-AU 11 85979947 85979947 single base substitution C A downstream_gene_variant MELA-AU 11 85979947 85979947 single base substitution C A intron_variant MELA-AU 11 85980461 85980461 single base substitution C T downstream_gene_variant MELA-AU 11 85980461 85980461 single base substitution C T intron_variant MELA-AU 11 85980851 85980851 single base substitution C T downstream_gene_variant MELA-AU 11 85980851 85980851 single base substitution C T intron_variant MELA-AU 11 85981035 85981035 single base substitution C T downstream_gene_variant MELA-AU 11 85981035 85981035 single base substitution C T intron_variant MELA-AU 11 85981341 85981342 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 85981341 85981342 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 85981648 85981648 single base substitution C T downstream_gene_variant MELA-AU 11 85981648 85981648 single base substitution C T intron_variant MELA-AU 11 85981660 85981660 single base substitution C T downstream_gene_variant MELA-AU 11 85981660 85981660 single base substitution C T intron_variant MELA-AU 11 85982218 85982218 single base substitution C G downstream_gene_variant MELA-AU 11 85982218 85982218 single base substitution C G intron_variant MELA-AU 11 85982218 85982218 single base substitution C G upstream_gene_variant MELA-AU 11 85982399 85982399 single base substitution T G downstream_gene_variant MELA-AU 11 85982399 85982399 single base substitution T G intron_variant MELA-AU 11 85982399 85982399 single base substitution T G upstream_gene_variant MELA-AU 11 85983971 85983971 single base substitution C T downstream_gene_variant MELA-AU 11 85983971 85983971 single base substitution C T intron_variant MELA-AU 11 85983971 85983971 single base substitution C T upstream_gene_variant MELA-AU 11 85984603 85984603 single base substitution C T intron_variant MELA-AU 11 85984603 85984603 single base substitution C T upstream_gene_variant MELA-AU 11 85984951 85984951 single base substitution C T intron_variant MELA-AU 11 85984951 85984951 single base substitution C T upstream_gene_variant MELA-AU 11 85985607 85985607 single base substitution G A intron_variant MELA-AU 11 85985607 85985607 single base substitution G A upstream_gene_variant MELA-AU 11 85985661 85985661 single base substitution G T intron_variant MELA-AU 11 85985661 85985661 single base substitution G T upstream_gene_variant MELA-AU 11 85985750 85985750 single base substitution C T intron_variant MELA-AU 11 85985750 85985750 single base substitution C T upstream_gene_variant MELA-AU 11 85985811 85985811 single base substitution C T intron_variant MELA-AU 11 85985811 85985811 single base substitution C T upstream_gene_variant MELA-AU 11 85985862 85985862 single base substitution C T intron_variant MELA-AU 11 85985862 85985862 single base substitution C T upstream_gene_variant MELA-AU 11 85986449 85986449 single base substitution C T intron_variant MELA-AU 11 85986449 85986449 single base substitution C T upstream_gene_variant MELA-AU 11 85987147 85987147 single base substitution C T intron_variant MELA-AU 11 85987147 85987147 single base substitution C T upstream_gene_variant MELA-AU 11 85988025 85988025 single base substitution T A 5_prime_UTR_variant MELA-AU 11 85988025 85988025 single base substitution T A exon_variant MELA-AU 11 85988025 85988025 single base substitution T A missense_variant C244S 730T>A MELA-AU 11 85988025 85988025 single base substitution T A missense_variant C324S 970T>A MELA-AU 11 85988025 85988025 single base substitution T A missense_variant C349S 1045T>A MELA-AU 11 85988025 85988025 single base substitution T A missense_variant C38S 112T>A MELA-AU 11 85988025 85988025 single base substitution T A upstream_gene_variant MELA-AU 11 85990215 85990215 single base substitution T C downstream_gene_variant MELA-AU 11 85990536 85990536 single base substitution C T downstream_gene_variant MELA-AU 11 85990537 85990537 single base substitution C T downstream_gene_variant MELA-AU 11 85990986 85990986 single base substitution C T downstream_gene_variant MELA-AU 11 85991097 85991097 single base substitution G A downstream_gene_variant MELA-AU 11 85991106 85991106 single base substitution T C downstream_gene_variant MELA-AU 11 85991409 85991409 single base substitution C T downstream_gene_variant MELA-AU 11 85992117 85992117 single base substitution A T downstream_gene_variant MELA-AU 11 85992323 85992323 single base substitution C T downstream_gene_variant MELA-AU 11 85992330 85992330 single base substitution G T downstream_gene_variant MELA-AU 11 85992499 85992499 single base substitution C T downstream_gene_variant MELA-AU 11 85992972 85992972 single base substitution G A downstream_gene_variant MELA-AU 11 85993307 85993307 single base substitution C T downstream_gene_variant MELA-AU 11 85993619 85993619 single base substitution G C downstream_gene_variant MELA-AU 11 85994431 85994431 single base substitution C T downstream_gene_variant MELA-AU 11 85994586 85994586 single base substitution C T downstream_gene_variant ORCA-IN 11 85963162 85963162 single base substitution C G intron_variant OV-AU 11 85952919 85952919 single base substitution T C upstream_gene_variant OV-AU 11 85954016 85954016 single base substitution G T upstream_gene_variant OV-AU 11 85961580 85961580 single base substitution C A intron_variant OV-AU 11 85962107 85962107 single base substitution T C intron_variant OV-AU 11 85962839 85962839 single base substitution A G intron_variant OV-AU 11 85962947 85962947 single base substitution G C intron_variant OV-AU 11 85964806 85964806 single base substitution G C intron_variant OV-AU 11 85967934 85967934 single base substitution A G intron_variant OV-AU 11 85971766 85971766 single base substitution A T intron_variant OV-AU 11 85971766 85971766 single base substitution A T upstream_gene_variant OV-AU 11 85977476 85977476 single base substitution G A intron_variant OV-AU 11 85977476 85977476 single base substitution G A upstream_gene_variant OV-AU 11 85985299 85985299 single base substitution T G intron_variant OV-AU 11 85985299 85985299 single base substitution T G upstream_gene_variant PACA-AU 11 85952279 85952279 single base substitution A C upstream_gene_variant PACA-AU 11 85953921 85953921 single base substitution T C upstream_gene_variant PACA-AU 11 85957732 85957732 insertion of <=200bp - T intron_variant PACA-AU 11 85959786 85959786 single base substitution C T intron_variant PACA-AU 11 85962347 85962347 single base substitution A G intron_variant PACA-AU 11 85967364 85967364 single base substitution T C intron_variant PACA-AU 11 85968688 85968688 single base substitution A G intron_variant PACA-AU 11 85968839 85968839 single base substitution G C intron_variant PACA-AU 11 85981585 85981585 single base substitution A T downstream_gene_variant PACA-AU 11 85981585 85981585 single base substitution A T intron_variant PACA-AU 11 85983885 85983885 single base substitution C T downstream_gene_variant PACA-AU 11 85983885 85983885 single base substitution C T intron_variant PACA-AU 11 85983885 85983885 single base substitution C T upstream_gene_variant PACA-AU 11 85987220 85987220 single base substitution C T 5_prime_UTR_variant PACA-AU 11 85987220 85987220 single base substitution C T intron_variant PACA-AU 11 85987220 85987220 single base substitution C T upstream_gene_variant PACA-AU 11 85991894 85991894 insertion of <=200bp - CTATTAT downstream_gene_variant PACA-AU 11 85992451 85992451 deletion of <=200bp T - downstream_gene_variant PACA-AU 11 85992821 85992821 single base substitution C T downstream_gene_variant PACA-CA 11 85950916 85950916 single base substitution T C upstream_gene_variant PACA-CA 11 85951022 85951022 single base substitution G A upstream_gene_variant PACA-CA 11 85952433 85952433 single base substitution C A upstream_gene_variant PACA-CA 11 85956043 85956043 single base substitution C A 5_prime_UTR_variant PACA-CA 11 85956043 85956043 single base substitution C A upstream_gene_variant PACA-CA 11 85958958 85958958 single base substitution C G intron_variant PACA-CA 11 85970825 85970825 single base substitution C G intron_variant PACA-CA 11 85970825 85970825 single base substitution C G upstream_gene_variant PACA-CA 11 85972025 85972025 single base substitution G A intron_variant PACA-CA 11 85972025 85972025 single base substitution G A upstream_gene_variant PACA-CA 11 85975008 85975008 insertion of <=200bp - G exon_variant PACA-CA 11 85975008 85975008 insertion of <=200bp - G intron_variant PACA-CA 11 85975008 85975008 insertion of <=200bp - G upstream_gene_variant PACA-CA 11 85980427 85980427 single base substitution C G downstream_gene_variant PACA-CA 11 85980427 85980427 single base substitution C G intron_variant PACA-CA 11 85987797 85987797 single base substitution T C 5_prime_UTR_variant PACA-CA 11 85987797 85987797 single base substitution T C intron_variant PACA-CA 11 85987797 85987797 single base substitution T C upstream_gene_variant PACA-CA 11 85990324 85990324 single base substitution G T downstream_gene_variant PACA-CA 11 85992771 85992771 single base substitution A G downstream_gene_variant PACA-CA 11 85994089 85994089 deletion of <=200bp A - downstream_gene_variant PAEN-AU 11 85973487 85973487 single base substitution A G intron_variant PAEN-AU 11 85973487 85973487 single base substitution A G upstream_gene_variant PBCA-DE 11 85952976 85952976 single base substitution C T upstream_gene_variant PBCA-DE 11 85956146 85956146 insertion of <=200bp - G 5_prime_UTR_variant PBCA-DE 11 85956146 85956146 insertion of <=200bp - G upstream_gene_variant PBCA-DE 11 85962072 85962072 single base substitution A G intron_variant PBCA-DE 11 85963555 85963555 single base substitution C T intron_variant PBCA-DE 11 85963557 85963557 single base substitution T C intron_variant PBCA-DE 11 85979286 85979286 single base substitution T A exon_variant PBCA-DE 11 85979286 85979286 single base substitution T A intron_variant PBCA-DE 11 85983969 85983969 single base substitution T C downstream_gene_variant PBCA-DE 11 85983969 85983969 single base substitution T C intron_variant PBCA-DE 11 85983969 85983969 single base substitution T C upstream_gene_variant PRAD-CA 11 85952180 85952180 single base substitution C A upstream_gene_variant PRAD-CA 11 85961377 85961377 single base substitution C T exon_variant PRAD-CA 11 85961377 85961377 single base substitution C T intron_variant PRAD-CA 11 85961377 85961377 single base substitution C T missense_variant R52C 154C>T PRAD-CA 11 85962456 85962456 single base substitution T A intron_variant PRAD-CA 11 85970265 85970265 single base substitution T A intron_variant PRAD-CA 11 85970265 85970265 single base substitution T A upstream_gene_variant PRAD-CA 11 85987193 85987193 single base substitution T C 5_prime_UTR_variant PRAD-CA 11 85987193 85987193 single base substitution T C intron_variant PRAD-CA 11 85987193 85987193 single base substitution T C upstream_gene_variant PRAD-UK 11 85951761 85951761 single base substitution A T upstream_gene_variant PRAD-UK 11 85954694 85954698 deletion of <=200bp ATGTC - upstream_gene_variant PRAD-UK 11 85955682 85955682 single base substitution C T 5_prime_UTR_variant PRAD-UK 11 85955682 85955682 single base substitution C T upstream_gene_variant PRAD-UK 11 85958019 85958019 single base substitution A G intron_variant PRAD-UK 11 85963557 85963557 insertion of <=200bp - CT intron_variant PRAD-UK 11 85967358 85967358 single base substitution A T intron_variant PRAD-UK 11 85985297 85985297 single base substitution T A intron_variant PRAD-UK 11 85985297 85985297 single base substitution T A upstream_gene_variant PRAD-UK 11 85992153 85992153 single base substitution G T downstream_gene_variant PRAD-US 11 85968564 85968564 single base substitution T G exon_variant PRAD-US 11 85968564 85968564 single base substitution T G intron_variant PRAD-US 11 85968564 85968564 single base substitution T G missense_variant V187G 560T>G RECA-EU 11 85954972 85954972 single base substitution C G upstream_gene_variant RECA-EU 11 85959997 85959997 single base substitution G A intron_variant RECA-EU 11 85969498 85969498 single base substitution C T intron_variant RECA-EU 11 85975000 85975000 single base substitution C A exon_variant RECA-EU 11 85975000 85975000 single base substitution C A intron_variant RECA-EU 11 85975000 85975000 single base substitution C A upstream_gene_variant RECA-EU 11 85977619 85977619 single base substitution A T intron_variant RECA-EU 11 85977619 85977619 single base substitution A T upstream_gene_variant RECA-EU 11 85979733 85979733 single base substitution G T downstream_gene_variant RECA-EU 11 85979733 85979733 single base substitution G T intron_variant RECA-EU 11 85983922 85983922 single base substitution A C downstream_gene_variant RECA-EU 11 85983922 85983922 single base substitution A C intron_variant RECA-EU 11 85983922 85983922 single base substitution A C upstream_gene_variant RECA-EU 11 85992592 85992592 single base substitution C A downstream_gene_variant SKCA-BR 11 85951223 85951223 single base substitution G T upstream_gene_variant SKCA-BR 11 85954249 85954249 single base substitution T C upstream_gene_variant SKCA-BR 11 85955613 85955613 single base substitution A G 5_prime_UTR_variant SKCA-BR 11 85955613 85955613 single base substitution A G upstream_gene_variant SKCA-BR 11 85956619 85956619 single base substitution G A intron_variant SKCA-BR 11 85957161 85957161 single base substitution T A intron_variant SKCA-BR 11 85960653 85960653 single base substitution G A intron_variant SKCA-BR 11 85960654 85960654 single base substitution G A intron_variant SKCA-BR 11 85962492 85962492 single base substitution G A intron_variant SKCA-BR 11 85963552 85963552 insertion of <=200bp - CA intron_variant SKCA-BR 11 85963554 85963554 insertion of <=200bp - TTC intron_variant SKCA-BR 11 85963556 85963556 single base substitution C T intron_variant SKCA-BR 11 85967709 85967709 single base substitution G A intron_variant SKCA-BR 11 85968037 85968037 single base substitution C T intron_variant SKCA-BR 11 85972274 85972274 single base substitution C T intron_variant SKCA-BR 11 85972274 85972274 single base substitution C T upstream_gene_variant SKCA-BR 11 85975357 85975357 single base substitution A C exon_variant SKCA-BR 11 85975357 85975357 single base substitution A C intron_variant SKCA-BR 11 85975357 85975357 single base substitution A C upstream_gene_variant SKCA-BR 11 85982959 85982959 single base substitution C T downstream_gene_variant SKCA-BR 11 85982959 85982959 single base substitution C T intron_variant SKCA-BR 11 85982959 85982959 single base substitution C T upstream_gene_variant SKCA-BR 11 85984380 85984380 single base substitution C T downstream_gene_variant SKCA-BR 11 85984380 85984380 single base substitution C T intron_variant SKCA-BR 11 85984380 85984380 single base substitution C T upstream_gene_variant SKCA-BR 11 85987277 85987277 single base substitution A C 5_prime_UTR_variant SKCA-BR 11 85987277 85987277 single base substitution A C intron_variant SKCA-BR 11 85987277 85987277 single base substitution A C upstream_gene_variant SKCA-BR 11 85990266 85990266 single base substitution T C downstream_gene_variant SKCA-BR 11 85994208 85994220 deletion of <=200bp GGCCCCTAAAGTT - downstream_gene_variant SKCM-US 11 85963196 85963196 single base substitution C T exon_variant SKCM-US 11 85963196 85963196 single base substitution C T intron_variant SKCM-US 11 85963196 85963196 single base substitution C T missense_variant H92Y 274C>T SKCM-US 11 85967484 85967484 single base substitution C T exon_variant SKCM-US 11 85967484 85967484 single base substitution C T intron_variant SKCM-US 11 85967484 85967484 single base substitution C T missense_variant P161L 482C>T SKCM-US 11 85975253 85975253 single base substitution T C exon_variant SKCM-US 11 85975253 85975253 single base substitution T C intron_variant SKCM-US 11 85975253 85975253 single base substitution T C missense_variant L225P 674T>C SKCM-US 11 85975253 85975253 single base substitution T C upstream_gene_variant SKCM-US 11 85988165 85988165 single base substitution G A exon_variant SKCM-US 11 85988165 85988165 single base substitution G A missense_variant M290I 870G>A SKCM-US 11 85988165 85988165 single base substitution G A missense_variant M35I 105G>A SKCM-US 11 85988165 85988165 single base substitution G A missense_variant M370I 1110G>A SKCM-US 11 85988165 85988165 single base substitution G A missense_variant M395I 1185G>A SKCM-US 11 85988165 85988165 single base substitution G A missense_variant M84I 252G>A SKCM-US 11 85989562 85989562 single base substitution C T 3_prime_UTR_variant SKCM-US 11 85989562 85989562 single base substitution C T downstream_gene_variant SKCM-US 11 85989562 85989562 single base substitution C T exon_variant SKCM-US 11 85989562 85989562 single base substitution C T stop_gained R106* 316C>T SKCM-US 11 85989562 85989562 single base substitution C T stop_gained R361* 1081C>T SKCM-US 11 85989562 85989562 single base substitution C T stop_gained R441* 1321C>T SKCM-US 11 85989562 85989562 single base substitution C T stop_gained R466* 1396C>T STAD-US 11 85961426 85961426 insertion of <=200bp - G exon_variant STAD-US 11 85961426 85961426 insertion of <=200bp - G frameshift_variant W68W? STAD-US 11 85961426 85961426 insertion of <=200bp - G intron_variant STAD-US 11 85963259 85963259 single base substitution T C exon_variant STAD-US 11 85963259 85963259 single base substitution T C intron_variant STAD-US 11 85963259 85963259 single base substitution T C missense_variant F113L 337T>C STAD-US 11 85967554 85967554 single base substitution G T intron_variant STAD-US 11 85967554 85967554 single base substitution G T missense_variant K184N 552G>T STAD-US 11 85967554 85967554 single base substitution G T splice_region_variant STAD-US 11 85975274 85975274 single base substitution T C exon_variant STAD-US 11 85975274 85975274 single base substitution T C intron_variant STAD-US 11 85975274 85975274 single base substitution T C missense_variant V232A 695T>C STAD-US 11 85975274 85975274 single base substitution T C upstream_gene_variant STAD-US 11 85977144 85977144 deletion of <=200bp A - exon_variant STAD-US 11 85977144 85977144 deletion of <=200bp A - frameshift_variant E249 STAD-US 11 85977144 85977144 deletion of <=200bp A - intron_variant STAD-US 11 85977144 85977144 deletion of <=200bp A - upstream_gene_variant STAD-US 11 85979585 85979585 single base substitution C T downstream_gene_variant STAD-US 11 85979585 85979585 single base substitution C T exon_variant STAD-US 11 85979585 85979585 single base substitution C T intron_variant STAD-US 11 85979585 85979585 single base substitution C T synonymous_variant G316G 948C>T THCA-SA 11 85968623 85968623 single base substitution C T exon_variant THCA-SA 11 85968623 85968623 single base substitution C T intron_variant THCA-SA 11 85968623 85968623 single base substitution C T synonymous_variant L207L 619C>T THCA-SA 11 85989676 85989676 single base substitution T C 3_prime_UTR_variant THCA-SA 11 85989676 85989676 single base substitution T C downstream_gene_variant THCA-SA 11 85989676 85989676 single base substitution T C exon_variant THCA-US 11 85956375 85956375 single base substitution G A exon_variant THCA-US 11 85956375 85956375 single base substitution G A missense_variant G33E 98G>A THCA-US 11 85956375 85956375 single base substitution G A missense_variant G35E 104G>A THCA-US 11 85977149 85977149 single base substitution A G exon_variant THCA-US 11 85977149 85977149 single base substitution A G intron_variant THCA-US 11 85977149 85977149 single base substitution A G missense_variant I251V 751A>G THCA-US 11 85977149 85977149 single base substitution A G upstream_gene_variant UCEC-US 11 85961343 85961343 single base substitution C T exon_variant UCEC-US 11 85961343 85961343 single base substitution C T intron_variant UCEC-US 11 85961343 85961343 single base substitution C T synonymous_variant D40D 120C>T UCEC-US 11 85961344 85961344 single base substitution G A exon_variant UCEC-US 11 85961344 85961344 single base substitution G A intron_variant UCEC-US 11 85961344 85961344 single base substitution G A missense_variant A41T 121G>A UCEC-US 11 85963241 85963241 single base substitution G A exon_variant UCEC-US 11 85963241 85963241 single base substitution G A intron_variant UCEC-US 11 85963241 85963241 single base substitution G A missense_variant E107K 319G>A UCEC-US 11 85967537 85967537 single base substitution A G exon_variant UCEC-US 11 85967537 85967537 single base substitution A G intron_variant UCEC-US 11 85967537 85967537 single base substitution A G missense_variant T179A 535A>G UCEC-US 11 85968611 85968611 single base substitution C A exon_variant UCEC-US 11 85968611 85968611 single base substitution C A intron_variant UCEC-US 11 85968611 85968611 single base substitution C A missense_variant P203T 607C>A UCEC-US 11 85975252 85975252 single base substitution C G exon_variant UCEC-US 11 85975252 85975252 single base substitution C G intron_variant UCEC-US 11 85975252 85975252 single base substitution C G missense_variant L225V 673C>G UCEC-US 11 85975252 85975252 single base substitution C G upstream_gene_variant UCEC-US 11 85977204 85977204 single base substitution G T exon_variant UCEC-US 11 85977204 85977204 single base substitution G T intron_variant UCEC-US 11 85977204 85977204 single base substitution G T missense_variant R269I 806G>T UCEC-US 11 85977204 85977204 single base substitution G T upstream_gene_variant UCEC-US 11 85977211 85977211 single base substitution G T exon_variant UCEC-US 11 85977211 85977211 single base substitution G T intron_variant UCEC-US 11 85977211 85977211 single base substitution G T missense_variant M271I 813G>T UCEC-US 11 85977211 85977211 single base substitution G T upstream_gene_variant UCEC-US 11 85979586 85979586 single base substitution G A downstream_gene_variant UCEC-US 11 85979586 85979586 single base substitution G A exon_variant UCEC-US 11 85979586 85979586 single base substitution G A intron_variant UCEC-US 11 85979586 85979586 single base substitution G A missense_variant D317N 949G>A UCEC-US 11 85988132 85988132 single base substitution C T exon_variant UCEC-US 11 85988132 85988132 single base substitution C T synonymous_variant S24S 72C>T UCEC-US 11 85988132 85988132 single base substitution C T synonymous_variant S279S 837C>T UCEC-US 11 85988132 85988132 single base substitution C T synonymous_variant S359S 1077C>T UCEC-US 11 85988132 85988132 single base substitution C T synonymous_variant S384S 1152C>T UCEC-US 11 85988132 85988132 single base substitution C T synonymous_variant S73S 219C>T UCEC-US 11 85988132 85988132 single base substitution C T upstream_gene_variant UCEC-US 11 85988963 85988963 single base substitution C A downstream_gene_variant UCEC-US 11 85988963 85988963 single base substitution C A exon_variant UCEC-US 11 85988963 85988963 single base substitution C A missense_variant L297I 889C>A UCEC-US 11 85988963 85988963 single base substitution C A missense_variant L377I 1129C>A UCEC-US 11 85988963 85988963 single base substitution C A missense_variant L402I 1204C>A UCEC-US 11 85988963 85988963 single base substitution C A missense_variant L42I 124C>A UCEC-US 11 85988963 85988963 single base substitution C A missense_variant L91I 271C>A UCEC-US 11 85989562 85989562 single base substitution C T 3_prime_UTR_variant UCEC-US 11 85989562 85989562 single base substitution C T downstream_gene_variant UCEC-US 11 85989562 85989562 single base substitution C T exon_variant UCEC-US 11 85989562 85989562 single base substitution C T stop_gained R106* 316C>T UCEC-US 11 85989562 85989562 single base substitution C T stop_gained R361* 1081C>T UCEC-US 11 85989562 85989562 single base substitution C T stop_gained R441* 1321C>T UCEC-US 11 85989562 85989562 single base substitution C T stop_gained R466* 1396C>T UCEC-US 11 85989563 85989563 single base substitution G A 3_prime_UTR_variant UCEC-US 11 85989563 85989563 single base substitution G A downstream_gene_variant UCEC-US 11 85989563 85989563 single base substitution G A exon_variant UCEC-US 11 85989563 85989563 single base substitution G A missense_variant R106Q 317G>A UCEC-US 11 85989563 85989563 single base substitution G A missense_variant R361Q 1082G>A UCEC-US 11 85989563 85989563 single base substitution G A missense_variant R441Q 1322G>A UCEC-US 11 85989563 85989563 single base substitution G A missense_variant R466Q 1397G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand B9-Tumor COSM3931460 c.624A>C p.S208S Substitution - coding silent 11:86257586-86257586 + Gp2D COSM2221612 c.213delA p.K72fs*14 Deletion - Frameshift 11:86250394-86250394 + CHC2048T COSM4793085 c.547A>G p.I183V Substitution - Missense 11:86256507-86256507 + B105-0 COSM1746620 c.484C>T p.L162L Substitution - coding silent 11:86256444-86256444 + CSCC-44-T COSM4445853 c.861-3C>T p.? Unknown 11:86268453-86268453 + TL42 COSM5751851 c.139_140insT p.G47fs*5 Insertion - Frameshift 11:86250320-86250321 + SH-1439 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + TCGA-AB-2876-03 COSM1318081 c.224C>A p.S75* Substitution - Nonsense 11:86250405-86250405 + SH-1362 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + SH-6055 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + TCGA-D9-A4Z3-01 COSM3454099 c.674T>C p.L225P Substitution - Missense 11:86264211-86264211 + SJTALL004 COSM305966 c.776C>T p.S259F Substitution - Missense 11:86266132-86266132 + SH-4435 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + SH-7032 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + TCGA-24-2289-01 COSM118652 c.33G>A p.A11A Substitution - coding silent 11:86245262-86245262 + TCGA-AP-A059-01 COSM932713 c.813G>T p.M271I Substitution - Missense 11:86266169-86266169 + 869586 COSM158750 c.587T>A p.L196Q Substitution - Missense 11:86257549-86257549 + TCGA-AA-A010-01 COSM280724 c.1172T>C p.L391S Substitution - Missense 11:86277964-86277964 + SNU-C2B COSM2221617 c.376T>C p.C126R Substitution - Missense 11:86255237-86255237 + 7073 COSM5751385 c.1240_1241insT p.R414fs*6 Insertion - Frameshift 11:86278439-86278440 + SH-3327 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + SH-3458 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + SH-8559 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + TCGA-AX-A0J1-01 COSM932707 c.121G>A p.A41T Substitution - Missense 11:86250302-86250302 + GC8_T COSM147298 c.1199+10T>C p.? Unknown 11:86278001-86278001 + TCGA-B5-A11E-01 COSM932717 c.1322G>A p.R441Q Substitution - Missense 11:86278521-86278521 + RK046_C01 COSM1628275 c.470A>G p.N157S Substitution - Missense 11:86256430-86256430 + TL76 COSM5752038 c.1306C>T p.R436C Substitution - Missense 11:86278505-86278505 + TCGA-AX-A0J0-01 COSM87721 c.949G>A p.D317N Substitution - Missense 11:86268544-86268544 + TCGA-F1-6177-01 COSM4037223 c.948C>T p.G316G Substitution - coding silent 11:86268543-86268543 + T3202 COSM4680238 c.27G>A p.A9A Substitution - coding silent 11:86245256-86245256 + 3988 COSM5751217 c.184G>AG p.A62fs*26 Complex - frameshift 11:86250365-86250365 + TCGA-AN-A046-01 COSM3810584 c.1064G>A p.R355Q Substitution - Missense 11:86277077-86277077 + TCGA-AX-A0J0-01 COSM932716 c.1321C>T p.R441* Substitution - Nonsense 11:86278520-86278520 + LUAD-YINHD COSM348548 c.690A>T p.G230G Substitution - coding silent 11:86264227-86264227 + PD8943a COSM3720451 c.904A>G p.R302G Substitution - Missense 11:86268499-86268499 + H_KA-869586G-S_16427 COSM158750 c.587T>A p.L196Q Substitution - Missense 11:86257549-86257549 + TCGA-DJ-A2Q0-01 COSM3368592 c.751A>G p.I251V Substitution - Missense 11:86266107-86266107 + CHC2048T COSM4793085 c.547A>G p.I183V Substitution - Missense 11:86256507-86256507 + SH-9248 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + TCGA-B5-A11E-01 COSM932708 c.319G>A p.E107K Substitution - Missense 11:86252199-86252199 + CP66-MEL COSM23374 c.508G>A p.G170S Substitution - Missense 11:86256468-86256468 + SC_9010 COSM5574127 c.267+8_267+9insA p.? Unknown 11:86250456-86250457 + TCGA-E2-A15E-01 COSM429982 c.230A>G p.K77R Substitution - Missense 11:86250411-86250411 + TCGA-EJ-5524-01 COSM1127622 c.560T>G p.V187G Substitution - Missense 11:86257522-86257522 + TCGA-E2-A15E-06 COSM429982 c.230A>G p.K77R Substitution - Missense 11:86250411-86250411 + TCGA-BH-A1FM-01 COSM1475948 c.424G>A p.D142N Substitution - Missense 11:86255285-86255285 + CN-AML-CR-23-Dx COSM5428098 c.211G>T p.G71* Substitution - Nonsense 11:86250392-86250392 + TCGA-FD-A3SO-01 COSM3792004 c.778C>T p.L260F Substitution - Missense 11:86266134-86266134 + T231 COSM4680239 c.137G>C p.S46T Substitution - Missense 11:86250318-86250318 + TCGA-EB-A299-01 COSM3454100 c.1110G>A p.M370I Substitution - Missense 11:86277123-86277123 + SH-102782 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + SKCO-1 COSM2221634 c.1054A>G p.I352V Substitution - Missense 11:86277067-86277067 + SH-7166 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + SH-1641 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + TCGA-HU-A4GX-01 COSM4037220 c.337T>C p.F113L Substitution - Missense 11:86252217-86252217 + Gp5D COSM2221612 c.213delA p.K72fs*14 Deletion - Frameshift 11:86250394-86250394 + TCGA-PD-A5DF-01 COSM4909768 c.685T>G p.F229V Substitution - Missense 11:86264222-86264222 + SH-2871 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + T368 COSM4680240 c.188C>A p.P63H Substitution - Missense 11:86250369-86250369 + SH-3133 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + CSCC-45-T COSM4501635 c.594C>T p.F198F Substitution - coding silent 11:86257556-86257556 + TCGA-D1-A167-01 COSM932714 c.1077C>T p.S359S Substitution - coding silent 11:86277090-86277090 + TCGA-DK-A3IT-01 COSM1298714 c.224C>G p.S75* Substitution - Nonsense 11:86250405-86250405 + 74 COSM4778182 c.223T>C p.S75P Substitution - Missense 11:86250404-86250404 + 19 COSM5747306 c.370T>C p.Y124H Substitution - Missense 11:86255231-86255231 + TCGA-FW-A3R5-06 COSM3870351 c.482C>T p.P161L Substitution - Missense 11:86256442-86256442 + TCGA-AP-A056-01 COSM932710 c.607C>A p.P203T Substitution - Missense 11:86257569-86257569 + TCGA-BR-8363-01 COSM4037222 c.695T>C p.V232A Substitution - Missense 11:86264232-86264232 + TCGA-BS-A0UF-01 COSM932712 c.806G>T p.R269I Substitution - Missense 11:86266162-86266162 + LUAD-S01405 COSM398906 c.1241G>C p.R414P Substitution - Missense 11:86278440-86278440 + 537 COSM3721602 c.1088T>C p.I363T Substitution - Missense 11:86277101-86277101 + CSCC-44-T COSM4507840 c.758C>T p.S253F Substitution - Missense 11:86266114-86266114 + TCGA-AP-A0LM-01 COSM932709 c.535A>G p.T179A Substitution - Missense 11:86256495-86256495 + TCGA-18-3410-01 COSM691224 c.788G>T p.W263L Substitution - Missense 11:86266144-86266144 + CPCG0249-F1 COSM4879954 c.154C>T p.R52C Substitution - Missense 11:86250335-86250335 + ESO-409 COSM1250947 c.1118G>A p.W373* Substitution - Nonsense 11:86277131-86277131 + A673 COSM2221609 c.28C>T p.P10S Substitution - Missense 11:86245257-86245257 + B105-0-Tumor COSM1746620 c.484C>T p.L162L Substitution - coding silent 11:86256444-86256444 + TCGA-AB-3009-03 COSM158750 c.587T>A p.L196Q Substitution - Missense 11:86257549-86257549 + TCGA-CD-8536-01 COSM4037221 c.552G>T p.K184N Substitution - Missense 11:86256512-86256512 + SH-9771 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + TCGA-BS-A0UV-01 COSM932706 c.120C>T p.D40D Substitution - coding silent 11:86250301-86250301 + LUAD-RT-S01831 COSM384241 c.288G>T p.L96F Substitution - Missense 11:86252168-86252168 + SJTALL004 COSM305966 c.776C>T p.S259F Substitution - Missense 11:86266132-86266132 + RK015_C COSM3700159 c.966+3A>G p.? Unknown 11:86268564-86268564 + TCGA-B0-5402-01 COSM467512 c.903C>T p.T301T Substitution - coding silent 11:86268498-86268498 + Gp5D COSM2221619 c.413A>T p.Y138F Substitution - Missense 11:86255274-86255274 + TCGA-D1-A17Q-01 COSM932712 c.806G>T p.R269I Substitution - Missense 11:86266162-86266162 + SH-7329 COSM429983 c.619C>T p.L207L Substitution - coding silent 11:86257581-86257581 + TCGA-CZ-4863-01 COSM467511 c.397C>T p.R133W Substitution - Missense 11:86255258-86255258 + TCGA-B5-A11R-01 COSM932711 c.673C>G p.L225V Substitution - Missense 11:86264210-86264210 + TCGA-AP-A059-01 COSM932715 c.1129C>A p.L377I Substitution - Missense 11:86277921-86277921 + TCGA-BH-A0W4-01 COSM429984 c.752T>C p.I251T Substitution - Missense 11:86266108-86266108 + TCGA-EL-A3CT-01 COSM3368591 c.104G>A p.G35E Substitution - Missense 11:86245333-86245333 + TCGA-GL-8500-01 COSM3986528 c.114T>A p.N38K Substitution - Missense 11:86245343-86245343 + TCGA-FW-A3R5-06 COSM932716 c.1321C>T p.R441* Substitution - Nonsense 11:86278520-86278520 + TCGA-18-3414-01 COSM691223 c.1116C>A p.F372L Substitution - Missense 11:86277129-86277129 + TCGA-GN-A266-06 COSM3454098 c.274C>T p.H92Y Substitution - Missense 11:86252154-86252154 + LP6005409-DNA_C01 COSM5951851 c.234C>T p.C78C Substitution - coding silent 11:86250415-86250415 + Gp2D COSM2221619 c.413A>T p.Y138F Substitution - Missense 11:86255274-86255274 + 24 COSM87721 c.949G>A p.D317N Substitution - Missense 11:86268544-86268544 + TCGA-24-0975-01 COSM118691 c.180A>G p.P60P Substitution - coding silent 11:86250361-86250361 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.503510 11q14.2-q22.3 605984

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.I319L c.955A>C 11 85979592 LUAD A G Missense p.I251V c.751A>G 11 85977149 THCA A G Missense p.K322E c.964A>G 11 85979601 LUAD A G Missense p.K77R c.230A>G 11 85961453 BRCA A G Missense p.N157S c.470A>G 11 85967472 HC A G Missense p.N204D c.610A>G 11 85968614 MM A G Missense p.T48A c.142A>G 11 85961365 LUAD A G Synonymous p.P60P c.180A>G 11 85961403 OV A T Synonymous p.A273A c.819A>T 11 85977217 HNSC C A Missense p.F372L c.1116C>A 11 85988171 LUSC C A Nonsense p.S75* c.224C>A 11 85961447 AML C G Missense p.L225V c.673C>G 11 85975252 UCEC C G Nonsense p.S75* c.224C>G 11 85961447 BLCA C T 5-UTRSNV . c.1-77C>T 11 85956195 CM C T IntronicSNV . c.861-7C>T 11 85979491 CM C T Nonsense p.Q292* c.874C>T 11 85979511 HNSC C T Nonsense p.R355* c.1063C>T 11 85988118 STAD C T Synonymous p.G316G c.948C>T 11 85979585 STAD G A IntronicSNV . c.635-57G>A 11 85975157 CM G A IntronicSNV . c.727-40G>A 11 85977085 CM G A Missense p.D142N c.424G>A 11 85966327 BRCA G A Missense p.M370I c.1110G>A 11 85988165 CM G A Nonsense p.W373* c.1118G>A 11 85988173 ESCA G A Synonymous p.A11A c.33G>A 11 85956304 OV G T Missense p.G117V c.350G>T 11 85963272 LUAD G T Missense p.W263L c.788G>T 11 85977186 LUSC T A IntronicSNV . c.360+1485T>A 11 85964767 CLL T A Missense p.L196Q c.587T>A 11 85968591 AML - TATT IntronicInsertion . c.726+177_726+178insTATT 11 85975482 CM T C IntronicSNV . c.726+406T>C 11 85975711 HC T C Missense p.I251T c.752T>C 11 85977150 BRCA T C Missense p.W263R c.787T>C 11 85977185 HNSC T - IntronicDeletion . c.635-1346delT 11 85973856 CM