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 36512195 36512195 + Silent SNP C C T TCGA-FD-A3SJ-01A-12D-A22Z-08 TCGA-FD-A3SJ-10A-01D-A22Z-08 g.chr11:36512195C>T c.762G>A c.(760-762)caG>caA p.Q254Q BLCA 11 36523047 36523047 + Missense_Mutation SNP C C T TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr11:36523047C>T c.19G>A c.(19-21)Gaa>Aaa p.E7K BRCA 11 36511783 36511783 + Missense_Mutation SNP G G A TCGA-A2-A4S1-01A-21D-A25Q-09 TCGA-A2-A4S1-10A-01D-A25Q-09 g.chr11:36511783G>A c.1174C>T c.(1174-1176)Cgc>Tgc p.R392C BRCA 11 36511852 36511852 + Missense_Mutation SNP C C T TCGA-AN-A0FT-01A-11W-A050-09 TCGA-AN-A0FT-10A-01W-A055-09 g.chr11:36511852C>T c.1105G>A c.(1105-1107)Gag>Aag p.E369K BRCA 11 36518707 36518707 + Missense_Mutation SNP T T C TCGA-E9-A243-01A-21D-A167-09 TCGA-E9-A243-10A-01D-A17G-09 g.chr11:36518707T>C c.557A>G c.(556-558)cAg>cGg p.Q186R BRCA 11 36518753 36518753 + Missense_Mutation SNP T T C TCGA-BH-A0B1-01A-12W-A071-09 TCGA-BH-A0B1-10A-01W-A071-09 g.chr11:36518753T>C c.511A>G c.(511-513)Aaa>Gaa p.K171E CESC 11 36511976 36511977 + Frame_Shift_Ins INS - - A TCGA-C5-A1BL-01A-11D-A13W-08 TCGA-C5-A1BL-10A-01D-A13W-08 g.chr11:36511976_36511977insA c.980_981insT c.(979-981)gtafs p.V327fs COAD 11 36511763 36511763 + Silent SNP C C T TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chr11:36511763C>T c.1194G>A c.(1192-1194)ccG>ccA p.P398P COAD 11 36511954 36511954 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:36511954G>A c.1003C>T c.(1003-1005)Cga>Tga p.R335* COAD 11 36512043 36512043 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr11:36512043C>T c.914G>A c.(913-915)cGc>cAc p.R305H COAD 11 36518807 36518807 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:36518807C>A c.457G>T c.(457-459)Gca>Tca p.A153S COAD 11 36520088 36520088 + Silent SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:36520088T>C c.399A>G c.(397-399)aaA>aaG p.K133K COAD 11 36522810 36522810 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:36522810C>T c.256G>A c.(256-258)Ggc>Agc p.G86S COADREAD 11 36511763 36511763 + Silent SNP C C T TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chr11:36511763C>T c.1194G>A c.(1192-1194)ccG>ccA p.P398P COADREAD 11 36511954 36511954 + Nonsense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:36511954G>A c.1003C>T c.(1003-1005)Cga>Tga p.R335* COADREAD 11 36512043 36512043 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr11:36512043C>T c.914G>A c.(913-915)cGc>cAc p.R305H COADREAD 11 36518807 36518807 + Missense_Mutation SNP C C A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:36518807C>A c.457G>T c.(457-459)Gca>Tca p.A153S COADREAD 11 36520088 36520088 + Silent SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:36520088T>C c.399A>G c.(397-399)aaA>aaG p.K133K COADREAD 11 36522810 36522810 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:36522810C>T c.256G>A c.(256-258)Ggc>Agc p.G86S DLBC 11 36518764 36518764 + Missense_Mutation SNP C C T TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr11:36518764C>T c.500G>A c.(499-501)cGt>cAt p.R167H ESCA 11 36522834 36522834 + Nonsense_Mutation SNP G G A TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr11:36522834G>A c.232C>T c.(232-234)Cga>Tga p.R78* GBMLGG 11 36511763 36511763 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:36511763C>T c.1194G>A c.(1192-1194)ccG>ccA p.P398P GBMLGG 11 36512016 36512016 + Missense_Mutation SNP C C A TCGA-HT-7607-01A-11D-2086-08 TCGA-HT-7607-10A-01D-2086-08 g.chr11:36512016C>A c.941G>T c.(940-942)cGg>cTg p.R314L GBMLGG 11 36512081 36512081 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:36512081G>A c.876C>T c.(874-876)gtC>gtT p.V292V HNSC 11 36514153 36514153 + Missense_Mutation SNP C C A TCGA-BB-A5HZ-01A-21D-A28R-08 TCGA-BB-A5HZ-10A-01D-A28U-08 g.chr11:36514153C>A c.704G>T c.(703-705)tGc>tTc p.C235F HNSC 11 36520057 36520057 + Missense_Mutation SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:36520057C>T c.430G>A c.(430-432)Gaa>Aaa p.E144K HNSC 11 36520173 36520173 + Missense_Mutation SNP C C T TCGA-CN-A63U-01A-11D-A30E-08 TCGA-CN-A63U-10A-01D-A30H-08 g.chr11:36520173C>T c.314G>A c.(313-315)tGt>tAt p.C105Y KIPAN 11 36511852 36511852 + Missense_Mutation SNP C C T TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr11:36511852C>T c.1105G>A c.(1105-1107)Gag>Aag p.E369K KIPAN 11 36514141 36514141 + Frame_Shift_Del DEL G G - TCGA-CZ-5467-01A-01D-1501-10 TCGA-CZ-5467-11A-01D-1501-10 g.chr11:36514141delG c.716delC c.(715-717)ccafs p.P239fs KIRC 11 36511852 36511852 + Missense_Mutation SNP C C T TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr11:36511852C>T c.1105G>A c.(1105-1107)Gag>Aag p.E369K KIRC 11 36514141 36514141 + Frame_Shift_Del DEL G G - TCGA-CZ-5467-01A-01D-1501-10 TCGA-CZ-5467-11A-01D-1501-10 g.chr11:36514141delG c.716delC c.(715-717)ccafs p.P239fs LGG 11 36511763 36511763 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:36511763C>T c.1194G>A c.(1192-1194)ccG>ccA p.P398P LGG 11 36512016 36512016 + Missense_Mutation SNP C C A TCGA-HT-7607-01A-11D-2086-08 TCGA-HT-7607-10A-01D-2086-08 g.chr11:36512016C>A c.941G>T c.(940-942)cGg>cTg p.R314L LGG 11 36512081 36512081 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:36512081G>A c.876C>T c.(874-876)gtC>gtT p.V292V LIHC 11 36511424 36511424 + Silent SNP C C T TCGA-MI-A75G-01A-11D-A32G-10 TCGA-MI-A75G-10A-01D-A32G-10 g.chr11:36511424C>T c.1533G>A c.(1531-1533)gaG>gaA p.E511E LIHC 11 36516546 36516546 + Missense_Mutation SNP T T C TCGA-G3-A25Z-01A-11D-A16V-10 TCGA-G3-A25Z-10A-01D-A16V-10 g.chr11:36516546T>C c.658A>G c.(658-660)Act>Gct p.T220A LIHC 11 36520043 36520043 + Silent SNP A A G TCGA-DD-A39Z-01A-11D-A20W-10 TCGA-DD-A39Z-11A-21D-A20W-10 g.chr11:36520043A>G c.444T>C c.(442-444)ctT>ctC p.L148L LIHC 11 36520132 36520132 + Missense_Mutation SNP G G T TCGA-DD-AADN-01A-11D-A40R-10 TCGA-DD-AADN-10A-01D-A40U-10 g.chr11:36520132G>T c.355C>A c.(355-357)Cca>Aca p.P119T LUAD 11 36511395 36511395 + Missense_Mutation SNP C C T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr11:36511395C>T c.1562G>A c.(1561-1563)gGg>gAg p.G521E LUAD 11 36511491 36511491 + Missense_Mutation SNP T T A TCGA-17-Z062-01A-01W-0747-08 TCGA-17-Z062-11A-01W-0747-08 g.chr11:36511491T>A c.1466A>T c.(1465-1467)aAg>aTg p.K489M LUAD 11 36511633 36511633 + Missense_Mutation SNP C C A TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr11:36511633C>A c.1324G>T c.(1324-1326)Gta>Tta p.V442L LUAD 11 36511802 36511802 + Silent SNP G G A TCGA-MN-A4N1-01A-11D-A24P-08 TCGA-MN-A4N1-10A-01D-A24P-08 g.chr11:36511802G>A c.1155C>T c.(1153-1155)ccC>ccT p.P385P LUAD 11 36511949 36511949 + Silent SNP G G A TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chr11:36511949G>A c.1008C>T c.(1006-1008)acC>acT p.T336T LUAD 11 36512083 36512083 + Missense_Mutation SNP C C A TCGA-53-7626-01A-12D-2063-08 TCGA-53-7626-10A-01D-2063-08 g.chr11:36512083C>A c.874G>T c.(874-876)Gtc>Ttc p.V292F LUAD 11 36512104 36512104 + Missense_Mutation SNP C C G TCGA-55-8205-01A-11D-2238-08 TCGA-55-8205-10A-01D-2238-08 g.chr11:36512104C>G c.853G>C c.(853-855)Gac>Cac p.D285H LUAD 11 36516548 36516548 + Missense_Mutation SNP T T C TCGA-55-6987-01A-11D-1945-08 TCGA-55-6987-11A-01D-1945-08 g.chr11:36516548T>C c.656A>G c.(655-657)aAt>aGt p.N219S LUAD 11 36520069 36520069 + Silent SNP A A G TCGA-38-4628-01A-01D-1265-08 TCGA-38-4628-11A-01D-1265-08 g.chr11:36520069A>G c.418T>C c.(418-420)Ttg>Ctg p.L140L LUSC 11 36511715 36511715 + Missense_Mutation SNP C C T TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr11:36511715C>T c.1242G>A c.(1240-1242)atG>atA p.M414I LUSC 11 36512059 36512059 + Missense_Mutation SNP G G T TCGA-51-4079-01A-01D-1458-08 TCGA-51-4079-11A-01D-1458-08 g.chr11:36512059G>T c.898C>A c.(898-900)Cac>Aac p.H300N LUSC 11 36514132 36514132 + Missense_Mutation SNP C C T TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr11:36514132C>T c.725G>A c.(724-726)tGc>tAc p.C242Y LUSC 11 36520129 36520129 + Missense_Mutation SNP C C T TCGA-21-1076-01A-02D-1521-08 TCGA-21-1076-11A-01D-1521-08 g.chr11:36520129C>T c.358G>A c.(358-360)Gac>Aac p.D120N LUSC 11 36522776 36522776 + Missense_Mutation SNP G G A TCGA-22-0944-01A-01D-1521-08 TCGA-22-0944-11A-01D-1521-08 g.chr11:36522776G>A c.290C>T c.(289-291)tCa>tTa p.S97L OV 11 36511516 36511516 + Missense_Mutation SNP C C T TCGA-61-1919-01A-01W-0699-08 TCGA-61-1919-11A-01W-0700-08 g.chr11:36511516C>T c.1441G>A c.(1441-1443)Gcc>Acc p.A481T OV 11 36511561 36511561 + Missense_Mutation SNP G G A TCGA-13-1410-01A-01W-0492-08 TCGA-13-1410-10A-01W-0493-08 g.chr11:36511561G>A c.1396C>T c.(1396-1398)Cgg>Tgg p.R466W PAAD 11 36518716 36518716 + Missense_Mutation SNP G G T TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr11:36518716G>T c.548C>A c.(547-549)cCa>cAa p.P183Q PRAD 11 36511471 36511471 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:36511471G>A c.1486C>T c.(1486-1488)Cgc>Tgc p.R496C PRAD 11 36511685 36511685 + Nonsense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:36511685C>T c.1272G>A c.(1270-1272)tgG>tgA p.W424* PRAD 11 36516553 36516553 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:36516553G>A c.651C>T c.(649-651)taC>taT p.Y217Y SARC 11 36511549 36511549 + Missense_Mutation SNP C C A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr11:36511549C>A c.1408G>T c.(1408-1410)Ggt>Tgt p.G470C SARC 11 36511818 36511818 + Missense_Mutation SNP A A T TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr11:36511818A>T c.1139T>A c.(1138-1140)tTc>tAc p.F380Y SKCM 11 36511689 36511689 + Missense_Mutation SNP G G A TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr11:36511689G>A c.1268C>T c.(1267-1269)cCt>cTt p.P423L SKCM 11 36511691 36511691 + Silent SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr11:36511691G>A c.1266C>T c.(1264-1266)ctC>ctT p.L422L SKCM 11 36511732 36511732 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr11:36511732G>A c.1225C>T c.(1225-1227)Ctt>Ttt p.L409F SKCM 11 36514136 36514136 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr11:36514136G>A c.721C>T c.(721-723)Cca>Tca p.P241S SKCM 11 36516595 36516595 + Silent SNP G G A TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr11:36516595G>A c.609C>T c.(607-609)atC>atT p.I203I SKCM 11 36520147 36520147 + Missense_Mutation SNP C C T TCGA-ER-A1A1-06A-11D-A197-08 TCGA-ER-A1A1-10A-01D-A199-08 g.chr11:36520147C>T c.340G>A c.(340-342)Gaa>Aaa p.E114K

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 11 36512195 36512195 single base substitution C T exon_variant BLCA-US 11 36512195 36512195 single base substitution C T synonymous_variant Q254Q 762G>A BLCA-US 11 36523047 36523047 single base substitution C T missense_variant E7K 19G>A BLCA-US 11 36523047 36523047 single base substitution C T upstream_gene_variant BOCA-UK 11 36520184 36520184 single base substitution T A synonymous_variant A101A 303A>T BOCA-UK 11 36520184 36520184 single base substitution T A upstream_gene_variant BRCA-EU 11 36504957 36504957 single base substitution G A downstream_gene_variant BRCA-EU 11 36509136 36509136 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 36509136 36509136 single base substitution G A downstream_gene_variant BRCA-EU 11 36510592 36510592 single base substitution G T 3_prime_UTR_variant BRCA-EU 11 36510592 36510592 single base substitution G T downstream_gene_variant BRCA-EU 11 36512382 36512382 deletion of <=200bp A - intron_variant BRCA-EU 11 36513048 36513051 deletion of <=200bp TGTT - intron_variant BRCA-EU 11 36513676 36513676 single base substitution C T intron_variant BRCA-EU 11 36515959 36515959 single base substitution A G intron_variant BRCA-EU 11 36520483 36520483 single base substitution G A intron_variant BRCA-EU 11 36520483 36520483 single base substitution G A upstream_gene_variant BRCA-EU 11 36521442 36521442 deletion of <=200bp C - intron_variant BRCA-EU 11 36521442 36521442 deletion of <=200bp C - upstream_gene_variant BRCA-EU 11 36521824 36521824 single base substitution T C intron_variant BRCA-EU 11 36521824 36521824 single base substitution T C upstream_gene_variant BRCA-EU 11 36525017 36525017 single base substitution G A intron_variant BRCA-EU 11 36525517 36525517 single base substitution A G intron_variant BRCA-EU 11 36526000 36526000 single base substitution C G intron_variant BRCA-EU 11 36526222 36526222 single base substitution T A intron_variant BRCA-EU 11 36526468 36526468 single base substitution G T intron_variant BRCA-EU 11 36526673 36526673 single base substitution C T intron_variant BRCA-EU 11 36527396 36527399 multiple base substitution (>=2bp and <=200bp) CTGA CCT intron_variant BRCA-EU 11 36530782 36530785 deletion of <=200bp AATT - intron_variant BRCA-EU 11 36530800 36530800 single base substitution G A intron_variant BRCA-EU 11 36530988 36530988 single base substitution T A intron_variant BRCA-EU 11 36531079 36531079 single base substitution A G intron_variant BRCA-EU 11 36532296 36532296 single base substitution C A upstream_gene_variant BRCA-EU 11 36533015 36533015 single base substitution G A upstream_gene_variant BRCA-EU 11 36535393 36535393 single base substitution C G upstream_gene_variant BRCA-EU 11 36535489 36535489 single base substitution A C upstream_gene_variant BRCA-EU 11 36536214 36536214 single base substitution C T upstream_gene_variant BRCA-FR 11 36519222 36519222 single base substitution T C intron_variant BRCA-FR 11 36519222 36519222 single base substitution T C upstream_gene_variant BRCA-FR 11 36526000 36526000 single base substitution C G intron_variant BRCA-FR 11 36526673 36526673 single base substitution C T intron_variant BRCA-UK 11 36530800 36530800 single base substitution G A intron_variant BRCA-UK 11 36536214 36536214 single base substitution C T upstream_gene_variant BRCA-US 11 36511783 36511783 single base substitution G A downstream_gene_variant BRCA-US 11 36511783 36511783 single base substitution G A missense_variant R392C 1174C>T BRCA-US 11 36511852 36511852 single base substitution C T downstream_gene_variant BRCA-US 11 36511852 36511852 single base substitution C T missense_variant E369K 1105G>A BRCA-US 11 36518707 36518707 single base substitution T C missense_variant Q186R 557A>G BRCA-US 11 36518707 36518707 single base substitution T C upstream_gene_variant BRCA-US 11 36518753 36518753 single base substitution T C missense_variant K171E 511A>G BRCA-US 11 36518753 36518753 single base substitution T C upstream_gene_variant BTCA-JP 11 36514086 36514086 deletion of <=200bp A - intron_variant BTCA-JP 11 36514086 36514086 insertion of <=200bp - A intron_variant CESC-US 11 36511976 36511976 insertion of <=200bp - A exon_variant CESC-US 11 36511976 36511976 insertion of <=200bp - A frameshift_variant V327V? COAD-US 11 36511763 36511763 single base substitution C T downstream_gene_variant COAD-US 11 36511763 36511763 single base substitution C T synonymous_variant P398P 1194G>A COCA-CN 11 36511403 36511403 single base substitution A T downstream_gene_variant COCA-CN 11 36511403 36511403 single base substitution A T synonymous_variant T518T 1554T>A COCA-CN 11 36511801 36511801 single base substitution C T downstream_gene_variant COCA-CN 11 36511801 36511801 single base substitution C T missense_variant G386R 1156G>A COCA-CN 11 36512240 36512240 single base substitution C T intron_variant COCA-CN 11 36514085 36514085 single base substitution G A intron_variant COCA-CN 11 36514290 36514290 single base substitution T C intron_variant COCA-CN 11 36520221 36520221 single base substitution T A intron_variant COCA-CN 11 36520221 36520221 single base substitution T A upstream_gene_variant COCA-CN 11 36523039 36523039 single base substitution G A synonymous_variant S9S 27C>T COCA-CN 11 36523039 36523039 single base substitution G A upstream_gene_variant ESAD-UK 11 36505056 36505056 single base substitution T C downstream_gene_variant ESAD-UK 11 36506176 36506176 single base substitution C T downstream_gene_variant ESAD-UK 11 36506451 36506451 single base substitution C A downstream_gene_variant ESAD-UK 11 36507667 36507667 single base substitution G A downstream_gene_variant ESAD-UK 11 36509225 36509225 single base substitution G A 3_prime_UTR_variant ESAD-UK 11 36509225 36509225 single base substitution G A downstream_gene_variant ESAD-UK 11 36511411 36511411 single base substitution G A downstream_gene_variant ESAD-UK 11 36511411 36511411 single base substitution G A stop_gained R516* 1546C>T ESAD-UK 11 36513098 36513098 single base substitution G C intron_variant ESAD-UK 11 36513292 36513292 single base substitution C T intron_variant ESAD-UK 11 36513580 36513580 single base substitution G A intron_variant ESAD-UK 11 36515937 36515937 single base substitution C A intron_variant ESAD-UK 11 36516850 36516850 single base substitution C T intron_variant ESAD-UK 11 36516944 36516944 single base substitution C T intron_variant ESAD-UK 11 36517324 36517324 single base substitution C T intron_variant ESAD-UK 11 36517903 36517903 single base substitution G A intron_variant ESAD-UK 11 36519813 36519813 insertion of <=200bp - A intron_variant ESAD-UK 11 36519813 36519813 insertion of <=200bp - A upstream_gene_variant ESAD-UK 11 36520105 36520105 single base substitution G T missense_variant L128I 382C>A ESAD-UK 11 36520105 36520105 single base substitution G T upstream_gene_variant ESAD-UK 11 36520744 36520744 single base substitution G C intron_variant ESAD-UK 11 36520744 36520744 single base substitution G C upstream_gene_variant ESAD-UK 11 36525765 36525765 single base substitution A C intron_variant ESAD-UK 11 36530659 36530659 single base substitution G C intron_variant ESAD-UK 11 36531922 36531922 single base substitution G T upstream_gene_variant ESAD-UK 11 36531923 36531923 single base substitution G T upstream_gene_variant ESAD-UK 11 36532368 36532368 single base substitution A G upstream_gene_variant ESAD-UK 11 36534470 36534470 single base substitution C T upstream_gene_variant ESAD-UK 11 36534713 36534713 single base substitution G A upstream_gene_variant ESAD-UK 11 36534835 36534835 single base substitution C G upstream_gene_variant ESAD-UK 11 36535006 36535006 single base substitution T C upstream_gene_variant ESAD-UK 11 36536176 36536176 single base substitution G A upstream_gene_variant ESAD-UK 11 36536699 36536699 single base substitution C G upstream_gene_variant GBM-US 11 36518817 36518817 single base substitution C A splice_acceptor_variant GBM-US 11 36518817 36518817 single base substitution C A upstream_gene_variant KIRC-US 11 36514141 36514141 deletion of <=200bp G - exon_variant KIRC-US 11 36514141 36514141 deletion of <=200bp G - frameshift_variant P239 LICA-FR 11 36511280 36511280 single base substitution T C 3_prime_UTR_variant LICA-FR 11 36511280 36511280 single base substitution T C downstream_gene_variant LICA-FR 11 36511910 36511910 single base substitution G A downstream_gene_variant LICA-FR 11 36511910 36511910 single base substitution G A synonymous_variant C349C 1047C>T LIHC-US 11 36511424 36511424 single base substitution C T downstream_gene_variant LIHC-US 11 36511424 36511424 single base substitution C T synonymous_variant E511E 1533G>A LIHC-US 11 36516546 36516546 single base substitution T C exon_variant LIHC-US 11 36516546 36516546 single base substitution T C missense_variant T220A 658A>G LINC-JP 11 36512190 36512190 single base substitution T C exon_variant LINC-JP 11 36512190 36512190 single base substitution T C missense_variant N256S 767A>G LINC-JP 11 36520110 36520110 single base substitution T C missense_variant E126G 377A>G LINC-JP 11 36520110 36520110 single base substitution T C upstream_gene_variant LIRI-JP 11 36506878 36506878 single base substitution T C downstream_gene_variant LIRI-JP 11 36508622 36508622 single base substitution C A 3_prime_UTR_variant LIRI-JP 11 36508622 36508622 single base substitution C A downstream_gene_variant LIRI-JP 11 36508748 36508748 single base substitution A C 3_prime_UTR_variant LIRI-JP 11 36508748 36508748 single base substitution A C downstream_gene_variant LIRI-JP 11 36510163 36510163 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 36510163 36510163 single base substitution A G downstream_gene_variant LIRI-JP 11 36510946 36510946 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 36510946 36510946 single base substitution G A downstream_gene_variant LIRI-JP 11 36511220 36511220 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 36511220 36511220 single base substitution G A downstream_gene_variant LIRI-JP 11 36511704 36511704 single base substitution T C downstream_gene_variant LIRI-JP 11 36511704 36511704 single base substitution T C missense_variant Y418C 1253A>G LIRI-JP 11 36512092 36512092 single base substitution T C exon_variant LIRI-JP 11 36512092 36512092 single base substitution T C missense_variant I289V 865A>G LIRI-JP 11 36514667 36514667 single base substitution T C intron_variant LIRI-JP 11 36515393 36515393 single base substitution T C intron_variant LIRI-JP 11 36515545 36515545 single base substitution C A intron_variant LIRI-JP 11 36515797 36515797 single base substitution G A intron_variant LIRI-JP 11 36517626 36517626 single base substitution G A intron_variant LIRI-JP 11 36517744 36517744 single base substitution T C intron_variant LIRI-JP 11 36518536 36518536 single base substitution A C intron_variant LIRI-JP 11 36518536 36518536 single base substitution A C upstream_gene_variant LIRI-JP 11 36519185 36519185 single base substitution T C intron_variant LIRI-JP 11 36519185 36519185 single base substitution T C upstream_gene_variant LIRI-JP 11 36520101 36520101 single base substitution G A missense_variant S129F 386C>T LIRI-JP 11 36520101 36520101 single base substitution G A upstream_gene_variant LIRI-JP 11 36520107 36520107 single base substitution A T missense_variant I127N 380T>A LIRI-JP 11 36520107 36520107 single base substitution A T upstream_gene_variant LIRI-JP 11 36520264 36520264 single base substitution T C intron_variant LIRI-JP 11 36520264 36520264 single base substitution T C upstream_gene_variant LIRI-JP 11 36520800 36520800 single base substitution T C intron_variant LIRI-JP 11 36520800 36520800 single base substitution T C upstream_gene_variant LIRI-JP 11 36522967 36522967 single base substitution A G synonymous_variant D33D 99T>C LIRI-JP 11 36522967 36522967 single base substitution A G upstream_gene_variant LIRI-JP 11 36522978 36522978 single base substitution C T missense_variant V30I 88G>A LIRI-JP 11 36522978 36522978 single base substitution C T upstream_gene_variant LIRI-JP 11 36523956 36523956 single base substitution G A intron_variant LIRI-JP 11 36524273 36524273 single base substitution A G intron_variant LIRI-JP 11 36525535 36525535 single base substitution C T intron_variant LIRI-JP 11 36525925 36525925 single base substitution C T intron_variant LIRI-JP 11 36526266 36526266 single base substitution T C intron_variant LIRI-JP 11 36526433 36526433 single base substitution C T intron_variant LIRI-JP 11 36526969 36526969 single base substitution G A intron_variant LIRI-JP 11 36527639 36527639 single base substitution G A intron_variant LIRI-JP 11 36528004 36528004 single base substitution T C intron_variant LIRI-JP 11 36528647 36528647 single base substitution A G intron_variant LIRI-JP 11 36530677 36530677 single base substitution T G intron_variant LIRI-JP 11 36535216 36535216 single base substitution G A upstream_gene_variant LIRI-JP 11 36536694 36536694 single base substitution G A upstream_gene_variant LUSC-KR 11 36514245 36514245 single base substitution C T intron_variant LUSC-KR 11 36528236 36528236 single base substitution C T intron_variant LUSC-KR 11 36531790 36531790 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 11 36533665 36533665 single base substitution G T upstream_gene_variant LUSC-KR 11 36534707 36534707 single base substitution T A upstream_gene_variant LUSC-KR 11 36536289 36536289 single base substitution C T upstream_gene_variant LUSC-US 11 36511715 36511715 single base substitution C T downstream_gene_variant LUSC-US 11 36511715 36511715 single base substitution C T missense_variant M414I 1242G>A LUSC-US 11 36512059 36512059 single base substitution G T exon_variant LUSC-US 11 36512059 36512059 single base substitution G T missense_variant H300N 898C>A LUSC-US 11 36514132 36514132 single base substitution C T exon_variant LUSC-US 11 36514132 36514132 single base substitution C T missense_variant C242Y 725G>A LUSC-US 11 36520129 36520129 single base substitution C T missense_variant D120N 358G>A LUSC-US 11 36520129 36520129 single base substitution C T upstream_gene_variant LUSC-US 11 36522776 36522776 single base substitution G A missense_variant S97L 290C>T LUSC-US 11 36522776 36522776 single base substitution G A upstream_gene_variant MALY-DE 11 36509954 36509954 single base substitution C T 3_prime_UTR_variant MALY-DE 11 36509954 36509954 single base substitution C T downstream_gene_variant MALY-DE 11 36511893 36511893 single base substitution C T downstream_gene_variant MALY-DE 11 36511893 36511893 single base substitution C T stop_gained W355* 1064G>A MALY-DE 11 36511915 36511915 single base substitution G A downstream_gene_variant MALY-DE 11 36511915 36511915 single base substitution G A stop_gained Q348* 1042C>T MALY-DE 11 36530419 36530419 single base substitution T C intron_variant MELA-AU 11 36504845 36504845 single base substitution G A downstream_gene_variant MELA-AU 11 36505580 36505580 single base substitution G A downstream_gene_variant MELA-AU 11 36505585 36505585 single base substitution G A downstream_gene_variant MELA-AU 11 36505892 36505892 single base substitution G A downstream_gene_variant MELA-AU 11 36506212 36506212 single base substitution G A downstream_gene_variant MELA-AU 11 36506903 36506903 single base substitution G A downstream_gene_variant MELA-AU 11 36507693 36507693 single base substitution G A downstream_gene_variant MELA-AU 11 36508579 36508579 single base substitution T C 3_prime_UTR_variant MELA-AU 11 36508579 36508579 single base substitution T C downstream_gene_variant MELA-AU 11 36510466 36510466 single base substitution G A 3_prime_UTR_variant MELA-AU 11 36510466 36510466 single base substitution G A downstream_gene_variant MELA-AU 11 36510884 36510884 single base substitution G A 3_prime_UTR_variant MELA-AU 11 36510884 36510884 single base substitution G A downstream_gene_variant MELA-AU 11 36510915 36510915 single base substitution T C 3_prime_UTR_variant MELA-AU 11 36510915 36510915 single base substitution T C downstream_gene_variant MELA-AU 11 36511732 36511732 single base substitution G A downstream_gene_variant MELA-AU 11 36511732 36511732 single base substitution G A missense_variant L409F 1225C>T MELA-AU 11 36514747 36514747 single base substitution G A intron_variant MELA-AU 11 36515330 36515330 single base substitution G A intron_variant MELA-AU 11 36515593 36515593 single base substitution G A intron_variant MELA-AU 11 36515706 36515706 single base substitution G A intron_variant MELA-AU 11 36516930 36516930 single base substitution C T intron_variant MELA-AU 11 36517379 36517379 single base substitution T C intron_variant MELA-AU 11 36518139 36518139 single base substitution A G intron_variant MELA-AU 11 36518139 36518139 single base substitution A G upstream_gene_variant MELA-AU 11 36518629 36518629 single base substitution G A intron_variant MELA-AU 11 36518629 36518629 single base substitution G A upstream_gene_variant MELA-AU 11 36518747 36518747 single base substitution G A missense_variant H173Y 517C>T MELA-AU 11 36518747 36518747 single base substitution G A upstream_gene_variant MELA-AU 11 36519096 36519096 single base substitution T A intron_variant MELA-AU 11 36519096 36519096 single base substitution T A upstream_gene_variant MELA-AU 11 36519203 36519203 single base substitution A T intron_variant MELA-AU 11 36519203 36519203 single base substitution A T upstream_gene_variant MELA-AU 11 36520028 36520028 single base substitution G A intron_variant MELA-AU 11 36520028 36520028 single base substitution G A upstream_gene_variant MELA-AU 11 36520843 36520843 single base substitution G A intron_variant MELA-AU 11 36520843 36520843 single base substitution G A upstream_gene_variant MELA-AU 11 36521087 36521087 single base substitution G T intron_variant MELA-AU 11 36521087 36521087 single base substitution G T upstream_gene_variant MELA-AU 11 36521711 36521711 single base substitution T C intron_variant MELA-AU 11 36521711 36521711 single base substitution T C upstream_gene_variant MELA-AU 11 36524393 36524393 single base substitution G A intron_variant MELA-AU 11 36525327 36525327 single base substitution C T intron_variant MELA-AU 11 36525722 36525722 single base substitution G A intron_variant MELA-AU 11 36525876 36525876 single base substitution T C intron_variant MELA-AU 11 36526847 36526847 single base substitution A G intron_variant MELA-AU 11 36527300 36527300 single base substitution T A intron_variant MELA-AU 11 36528004 36528004 single base substitution T A intron_variant MELA-AU 11 36529762 36529762 single base substitution G A intron_variant MELA-AU 11 36530030 36530030 single base substitution G A intron_variant MELA-AU 11 36531216 36531216 single base substitution G C intron_variant MELA-AU 11 36531449 36531449 single base substitution G A intron_variant MELA-AU 11 36531906 36531907 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 36531964 36531964 single base substitution C T upstream_gene_variant MELA-AU 11 36533344 36533344 single base substitution G A upstream_gene_variant MELA-AU 11 36533598 36533599 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 36534607 36534607 single base substitution C T upstream_gene_variant MELA-AU 11 36534954 36534954 single base substitution C T upstream_gene_variant MELA-AU 11 36534967 36534967 single base substitution G A upstream_gene_variant MELA-AU 11 36535740 36535740 single base substitution C T upstream_gene_variant MELA-AU 11 36535915 36535915 single base substitution C T upstream_gene_variant MELA-AU 11 36536373 36536373 single base substitution C T upstream_gene_variant MELA-AU 11 36536521 36536521 single base substitution C T upstream_gene_variant OV-AU 11 36508129 36508129 single base substitution C T downstream_gene_variant OV-AU 11 36512150 36512150 single base substitution G T exon_variant OV-AU 11 36512150 36512150 single base substitution G T missense_variant H269Q 807C>A OV-AU 11 36529427 36529427 single base substitution T C intron_variant OV-AU 11 36529634 36529634 single base substitution C T intron_variant OV-AU 11 36532941 36532941 single base substitution C T upstream_gene_variant OV-AU 11 36534297 36534297 single base substitution C T upstream_gene_variant PACA-AU 11 36506925 36506925 single base substitution C T downstream_gene_variant PACA-AU 11 36509419 36509419 single base substitution C T 3_prime_UTR_variant PACA-AU 11 36509419 36509419 single base substitution C T downstream_gene_variant PACA-AU 11 36520655 36520672 deletion of <=200bp GTGAGGTCACATTTTAAA - intron_variant PACA-AU 11 36520655 36520672 deletion of <=200bp GTGAGGTCACATTTTAAA - upstream_gene_variant PACA-AU 11 36522818 36522818 single base substitution G A missense_variant T83M 248C>T PACA-AU 11 36522818 36522818 single base substitution G A upstream_gene_variant PACA-AU 11 36523928 36523928 single base substitution C T intron_variant PACA-AU 11 36525162 36525162 single base substitution C A intron_variant PACA-AU 11 36533113 36533137 deletion of <=200bp ATGCTTCTCTTTTTAAGAAGAATTT - upstream_gene_variant PACA-CA 11 36505130 36505130 single base substitution G A downstream_gene_variant PACA-CA 11 36510286 36510286 single base substitution T G 3_prime_UTR_variant PACA-CA 11 36510286 36510286 single base substitution T G downstream_gene_variant PACA-CA 11 36523206 36523208 deletion of <=200bp TAA - intron_variant PACA-CA 11 36530481 36530482 deletion of <=200bp TT - intron_variant PACA-CA 11 36535140 36535140 single base substitution T A upstream_gene_variant PBCA-DE 11 36510547 36510547 single base substitution G A 3_prime_UTR_variant PBCA-DE 11 36510547 36510547 single base substitution G A downstream_gene_variant PBCA-DE 11 36514796 36514796 single base substitution C A intron_variant PBCA-DE 11 36517979 36517979 single base substitution T C exon_variant PBCA-DE 11 36517979 36517979 single base substitution T C intron_variant PBCA-DE 11 36530707 36530707 single base substitution A G intron_variant PBCA-DE 11 36536028 36536028 single base substitution T C upstream_gene_variant PRAD-CA 11 36515414 36515414 single base substitution A G intron_variant PRAD-CA 11 36518138 36518138 single base substitution G A intron_variant PRAD-CA 11 36518138 36518138 single base substitution G A upstream_gene_variant PRAD-CA 11 36528424 36528424 single base substitution T G intron_variant PRAD-UK 11 36504586 36504586 deletion of <=200bp C - downstream_gene_variant PRAD-UK 11 36511486 36511486 single base substitution C G downstream_gene_variant PRAD-UK 11 36511486 36511486 single base substitution C G missense_variant D491H 1471G>C PRAD-UK 11 36522303 36522303 insertion of <=200bp - T intron_variant PRAD-UK 11 36522303 36522303 insertion of <=200bp - T upstream_gene_variant PRAD-UK 11 36522306 36522306 insertion of <=200bp - T intron_variant PRAD-UK 11 36522306 36522306 insertion of <=200bp - T upstream_gene_variant PRAD-UK 11 36527477 36527477 single base substitution T C intron_variant PRAD-UK 11 36535095 36535095 single base substitution C T upstream_gene_variant RECA-EU 11 36507836 36507836 single base substitution G A downstream_gene_variant RECA-EU 11 36508860 36508860 single base substitution G T 3_prime_UTR_variant RECA-EU 11 36508860 36508860 single base substitution G T downstream_gene_variant RECA-EU 11 36523634 36523634 single base substitution C T intron_variant RECA-EU 11 36525286 36525286 single base substitution G A intron_variant RECA-EU 11 36533651 36533651 single base substitution T A upstream_gene_variant SKCA-BR 11 36508427 36508427 single base substitution T G downstream_gene_variant SKCA-BR 11 36513221 36513221 single base substitution C T intron_variant SKCA-BR 11 36516316 36516316 single base substitution G A intron_variant SKCA-BR 11 36517623 36517623 single base substitution G A intron_variant SKCA-BR 11 36524925 36524925 single base substitution A C intron_variant SKCA-BR 11 36528068 36528068 single base substitution A C intron_variant SKCA-BR 11 36528515 36528515 single base substitution T A intron_variant SKCA-BR 11 36528734 36528734 single base substitution T C intron_variant SKCA-BR 11 36528996 36528996 single base substitution A G intron_variant SKCA-BR 11 36531505 36531505 single base substitution A C intron_variant SKCA-BR 11 36533753 36533753 single base substitution G A upstream_gene_variant SKCA-BR 11 36534798 36534798 single base substitution C T upstream_gene_variant SKCM-US 11 36511689 36511689 single base substitution G A downstream_gene_variant SKCM-US 11 36511689 36511689 single base substitution G A missense_variant P423L 1268C>T SKCM-US 11 36511691 36511691 single base substitution G A downstream_gene_variant SKCM-US 11 36511691 36511691 single base substitution G A synonymous_variant L422L 1266C>T SKCM-US 11 36511732 36511732 single base substitution G A downstream_gene_variant SKCM-US 11 36511732 36511732 single base substitution G A missense_variant L409F 1225C>T SKCM-US 11 36511831 36511831 single base substitution G A downstream_gene_variant SKCM-US 11 36511831 36511831 single base substitution G A missense_variant H376Y 1126C>T SKCM-US 11 36514136 36514136 single base substitution G A exon_variant SKCM-US 11 36514136 36514136 single base substitution G A missense_variant P241S 721C>T SKCM-US 11 36516595 36516595 single base substitution G A splice_region_variant SKCM-US 11 36520147 36520147 single base substitution C T missense_variant E114K 340G>A SKCM-US 11 36520147 36520147 single base substitution C T upstream_gene_variant STAD-US 11 36511400 36511400 single base substitution A G downstream_gene_variant STAD-US 11 36511400 36511400 single base substitution A G synonymous_variant D519D 1557T>C STAD-US 11 36511764 36511764 single base substitution G A downstream_gene_variant STAD-US 11 36511764 36511764 single base substitution G A missense_variant P398L 1193C>T STAD-US 11 36512014 36512014 single base substitution C T exon_variant STAD-US 11 36512014 36512014 single base substitution C T missense_variant E315K 943G>A STAD-US 11 36512115 36512115 single base substitution C T exon_variant STAD-US 11 36512115 36512115 single base substitution C T missense_variant S281N 842G>A STAD-US 11 36516539 36516539 single base substitution A G exon_variant STAD-US 11 36516539 36516539 single base substitution A G missense_variant L222P 665T>C STAD-US 11 36520142 36520142 single base substitution A T missense_variant N115K 345T>A STAD-US 11 36520142 36520142 single base substitution A T upstream_gene_variant STAD-US 11 36520186 36520186 single base substitution C T missense_variant A101T 301G>A STAD-US 11 36520186 36520186 single base substitution C T upstream_gene_variant UCEC-US 11 36511471 36511471 single base substitution G A downstream_gene_variant UCEC-US 11 36511471 36511471 single base substitution G A missense_variant R496C 1486C>T UCEC-US 11 36511654 36511654 single base substitution G T downstream_gene_variant UCEC-US 11 36511654 36511654 single base substitution G T missense_variant L435I 1303C>A UCEC-US 11 36511743 36511743 single base substitution T C downstream_gene_variant UCEC-US 11 36511743 36511743 single base substitution T C missense_variant N405S 1214A>G UCEC-US 11 36511764 36511764 single base substitution G A downstream_gene_variant UCEC-US 11 36511764 36511764 single base substitution G A missense_variant P398L 1193C>T UCEC-US 11 36511925 36511925 single base substitution G A downstream_gene_variant UCEC-US 11 36511925 36511925 single base substitution G A synonymous_variant I344I 1032C>T UCEC-US 11 36511954 36511954 single base substitution G A exon_variant UCEC-US 11 36511954 36511954 single base substitution G A stop_gained R335* 1003C>T UCEC-US 11 36516536 36516536 single base substitution A G exon_variant UCEC-US 11 36516536 36516536 single base substitution A G missense_variant I223T 668T>C UCEC-US 11 36516569 36516569 single base substitution T C exon_variant UCEC-US 11 36516569 36516569 single base substitution T C missense_variant N212S 635A>G

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand AB COSM5414781 c.485G>A p.C162Y Substitution - Missense 11:36497229-36497229 - TCGA-AX-A0J1-01 COSM926721 c.1486C>T p.R496C Substitution - Missense 11:36489921-36489921 - TCGA-46-3769-01 COSM687421 c.1242G>A p.M414I Substitution - Missense 11:36490165-36490165 - ESO-0025 COSM1268458 c.541_549delGATTGTCCA p.D181_P183delDCP Deletion - In frame 11:36497165-36497173 - TCGA-BR-6452-01 COSM4032609 c.665T>C p.L222P Substitution - Missense 11:36494989-36494989 - AOCS-034-3-8 COSM3943648 c.807C>A p.H269Q Substitution - Missense 11:36490600-36490600 - TCGA-06-0190-02 COSM3397655 c.448-1G>T p.? Unknown 11:36497267-36497267 - TCGA-BS-A0UM-01 COSM926725 c.764G>T p.R255M Substitution - Missense 11:36490643-36490643 - ESO-085 COSM1268459 c.349C>T p.L117L Substitution - coding silent 11:36498588-36498588 - ME049T COSM230225 c.818T>C p.L273S Substitution - Missense 11:36490589-36490589 - TCGA-B0-5694-01 COSM466780 c.564T>C p.S188S Substitution - coding silent 11:36497150-36497150 - NYU695 COSM4770820 c.969G>T p.Q323H Substitution - Missense 11:36490438-36490438 - S00050 COSM318172 c.1006A>T p.T336S Substitution - Missense 11:36490401-36490401 - TCGA-22-0944-01 COSM687417 c.290C>T p.S97L Substitution - Missense 11:36501226-36501226 - TCGA-AA-A010-01 COSM285912 c.1003C>T p.R335* Substitution - Nonsense 11:36490404-36490404 - RK167_C01 COSM1627961 c.99T>C p.D33D Substitution - coding silent 11:36501417-36501417 - SH-0622 COSM5018360 c.1444delC p.L482fs*1 Deletion - Frameshift 11:36489963-36489963 - CSCC-42-T COSM3447044 c.517C>T p.H173Y Substitution - Missense 11:36497197-36497197 - YUTEPA COSM1703817 c.1303C>T p.L435F Substitution - Missense 11:36490104-36490104 - TCGA-21-1076-01 COSM687418 c.358G>A p.D120N Substitution - Missense 11:36498579-36498579 - HCC72T COSM1604518 c.377A>G p.E126G Substitution - Missense 11:36498560-36498560 - 5 COSM5014988 c.1204C>T p.R402C Substitution - Missense 11:36490203-36490203 - ESO-165 COSM1268460 c.362A>G p.N121S Substitution - Missense 11:36498575-36498575 - TCGA-D1-A15X-01 COSM926723 c.1214A>G p.N405S Substitution - Missense 11:36490193-36490193 - TCGA-EE-A2GP-06 COSM3447043 c.609C>T p.I203I Substitution - coding silent 11:36495045-36495045 - 06-P036 COSM4574349 c.240A>G p.A80A Substitution - coding silent 11:36501276-36501276 - TCGA-AP-A056-01 COSM926722 c.1303C>A p.L435I Substitution - Missense 11:36490104-36490104 - YUGURT COSM5372412 c.1233C>T p.V411V Substitution - coding silent 11:36490174-36490174 - 3N24-VS-3T24 COSM3791465 c.762G>A p.Q254Q Substitution - coding silent 11:36490645-36490645 - TCGA-G3-A25Z-01 COSM4922199 c.658A>G p.T220A Substitution - Missense 11:36494996-36494996 - S00050 COSM318172 c.1006A>T p.T336S Substitution - Missense 11:36490401-36490401 - YUTEPA COSM1703816 c.1525C>T p.R509W Substitution - Missense 11:36489882-36489882 - K277 COSM249574 c.815T>C p.M272T Substitution - Missense 11:36490592-36490592 - Capan-1 COSM328289 c.1313C>G p.S438C Substitution - Missense 11:36490094-36490094 - Pat_05_A COSM5838487 c.578C>T p.A193V Substitution - Missense 11:36497136-36497136 - CSCC-38-T COSM4462930 c.1267C>T p.P423S Substitution - Missense 11:36490140-36490140 - RK283_C01 COSM4780809 c.88G>A p.V30I Substitution - Missense 11:36501428-36501428 - HCC72 COSM1604518 c.377A>G p.E126G Substitution - Missense 11:36498560-36498560 - ESOSCC155T COSM1171778 c.1052G>C p.G351A Substitution - Missense 11:36490355-36490355 - CRC-03T COSM5451135 c.1554T>A p.T518T Substitution - coding silent 11:36489853-36489853 - 2492729 COSM5726400 c.923G>A p.R308K Substitution - Missense 11:36490484-36490484 - OST10T COSM1732587 c.1490G>T p.C497F Substitution - Missense 11:36489917-36489917 - TCGA-51-4079-01 COSM687420 c.898C>A p.H300N Substitution - Missense 11:36490509-36490509 - 8015299 COSM3769288 c.248C>T p.T83M Substitution - Missense 11:36501268-36501268 - 0045_CRUK_PC_0045_T1_DNA COSM5422130 c.1471G>C p.D491H Substitution - Missense 11:36489936-36489936 - SA223 COSM212503 c.1175G>A p.R392H Substitution - Missense 11:36490232-36490232 - TCGA-HU-A4GN-01 COSM4032606 c.1557T>C p.D519D Substitution - coding silent 11:36489850-36489850 - 587234 COSM1230215 c.995G>A p.R332Q Substitution - Missense 11:36490412-36490412 - TCGA-BR-6802-01 COSM4032610 c.345T>A p.N115K Substitution - Missense 11:36498592-36498592 - TCGA-D3-A3MR-06 COSM3447039 c.1268C>T p.P423L Substitution - Missense 11:36490139-36490139 - TCGA-CM-6680-01 COSM1353711 c.1194G>A p.P398P Substitution - coding silent 11:36490213-36490213 - TCGA-B4-5838-01 COSM428952 c.1105G>A p.E369K Substitution - Missense 11:36490302-36490302 - TCGA-61-1919-01 COSM117289 c.1441G>A p.A481T Substitution - Missense 11:36489966-36489966 - Gp2D COSM1978213 c.729A>G p.T243T Substitution - coding silent 11:36492578-36492578 - PD6345a COSM1636849 c.303A>T p.A101A Substitution - coding silent 11:36498634-36498634 - PT42 COSM5925647 c.607-3C>T p.? Unknown 11:36495050-36495050 - TCGA-A5-A0VP-01 COSM926727 c.635A>G p.N212S Substitution - Missense 11:36495019-36495019 - RK104_C01 COSM3700062 c.865A>G p.I289V Substitution - Missense 11:36490542-36490542 - HCC8T COSM1604517 c.767A>G p.N256S Substitution - Missense 11:36490640-36490640 - GCT77 COSM1978216 c.580G>A p.A194T Substitution - Missense 11:36497134-36497134 - LUAD-B02077 COSM334978 c.867C>G p.I289M Substitution - Missense 11:36490540-36490540 - CSCC-55-T COSM4526455 c.1397G>A p.R466Q Substitution - Missense 11:36490010-36490010 - TCGA-EE-A2GC-06 COSM3447042 c.721C>T p.P241S Substitution - Missense 11:36492586-36492586 - TCGA-AN-A0FT-01 COSM428952 c.1105G>A p.E369K Substitution - Missense 11:36490302-36490302 - S02287 COSM5685574 c.523A>G p.N175D Substitution - Missense 11:36497191-36497191 - HX14T COSM1604517 c.767A>G p.N256S Substitution - Missense 11:36490640-36490640 - TCGA-AA-A010-01 COSM285913 c.399A>G p.K133K Substitution - coding silent 11:36498538-36498538 - TCGA-ER-A1A1-06 COSM3447045 c.340G>A p.E114K Substitution - Missense 11:36498597-36498597 - TCGA-AP-A059-01 COSM926724 c.1032C>T p.I344I Substitution - coding silent 11:36490375-36490375 - TCGA-EE-A3JD-06 COSM4394442 c.1225C>T p.L409F Substitution - Missense 11:36490182-36490182 - TCGA-BG-A0M4-01 COSM926726 c.668T>C p.I223T Substitution - Missense 11:36494986-36494986 - TCGA-A2-A4S1-01 COSM1978206 c.1174C>T p.R392C Substitution - Missense 11:36490233-36490233 - TCGA-ER-A194-01 COSM3447041 c.1126C>T p.H376Y Substitution - Missense 11:36490281-36490281 - TCGA-E9-A243-01 COSM1475404 c.557A>G p.Q186R Substitution - Missense 11:36497157-36497157 - TCGA-FD-A3SJ-01 COSM3791465 c.762G>A p.Q254Q Substitution - coding silent 11:36490645-36490645 - 174T COSM1725962 c.239C>T p.A80V Substitution - Missense 11:36501277-36501277 - TCGA-66-2773-01 COSM687419 c.725G>A p.C242Y Substitution - Missense 11:36492582-36492582 - TCGA-13-1410-01 COSM73056 c.1396C>T p.R466W Substitution - Missense 11:36490011-36490011 - TCGA-AP-A0LM-01 COSM285912 c.1003C>T p.R335* Substitution - Nonsense 11:36490404-36490404 - 18195 COSM1298009 c.19G>A p.E7K Substitution - Missense 11:36501497-36501497 - Au5 COSM5606135 c.1454G>A p.R485K Substitution - Missense 11:36489953-36489953 - 23 COSM5014989 c.810G>T p.M270I Substitution - Missense 11:36490597-36490597 - TCGA-EE-A2GI-06 COSM3447040 c.1266C>T p.L422L Substitution - coding silent 11:36490141-36490141 - TCGA-MI-A75G-01 COSM4940106 c.1533G>A p.E511E Substitution - coding silent 11:36489874-36489874 - GCT27 COSM5749480 c.1391T>C p.I464T Substitution - Missense 11:36490016-36490016 - TCGA-AA-3672-01 COSM267628 c.457G>T p.A153S Substitution - Missense 11:36497257-36497257 - TCGA-BR-8361-01 COSM370398 c.1193C>T p.P398L Substitution - Missense 11:36490214-36490214 - TCGA-AP-A051-01 COSM926724 c.1032C>T p.I344I Substitution - coding silent 11:36490375-36490375 - LUAD-NYU160 COSM370398 c.1193C>T p.P398L Substitution - Missense 11:36490214-36490214 - tumor_4119279 COSM5946991 c.1064G>A p.W355* Substitution - Nonsense 11:36490343-36490343 - TCGA-D9-A4Z6-01 COSM3447044 c.517C>T p.H173Y Substitution - Missense 11:36497197-36497197 - S01170 COSM5666999 c.1144A>T p.T382S Substitution - Missense 11:36490263-36490263 - CHC1079T COSM4791120 c.1047C>T p.C349C Substitution - coding silent 11:36490360-36490360 - TCGA-BR-8360-01 COSM4032611 c.301G>A p.A101T Substitution - Missense 11:36498636-36498636 - T3174 COSM4735719 c.373C>T p.R125C Substitution - Missense 11:36498564-36498564 - TCGA-AP-A059-01 COSM370398 c.1193C>T p.P398L Substitution - Missense 11:36490214-36490214 - CHC1079T COSM4791120 c.1047C>T p.C349C Substitution - coding silent 11:36490360-36490360 - TCGA-BH-A0B1-01 COSM428953 c.511A>G p.K171E Substitution - Missense 11:36497203-36497203 - tumor_4176133 COSM5948256 c.1042C>T p.Q348* Substitution - Nonsense 11:36490365-36490365 - CHEWS003 COSM4574348 c.1321C>A p.P441T Substitution - Missense 11:36490086-36490086 - 88 COSM5014990 c.177G>C p.E59D Substitution - Missense 11:36501339-36501339 - 585210 COSM323962 c.871G>A p.E291K Substitution - Missense 11:36490536-36490536 - Gp5D COSM1978213 c.729A>G p.T243T Substitution - coding silent 11:36492578-36492578 - TCGA-CG-5733-01 COSM4032607 c.943G>A p.E315K Substitution - Missense 11:36490464-36490464 - 395 COSM4428619 c.325A>C p.N109H Substitution - Missense 11:36498612-36498612 - TCGA-BR-8080-01 COSM4032608 c.842G>A p.S281N Substitution - Missense 11:36490565-36490565 - 3N49-VS-3T49 COSM4982840 c.1479A>T p.L493F Substitution - Missense 11:36489928-36489928 - sysucc-1397T COSM5473124 c.1156G>A p.G386R Substitution - Missense 11:36490251-36490251 - BK0006 COSM4185604 c.1264C>A p.L422I Substitution - Missense 11:36490143-36490143 - TCGA-E5-A2PC-01 COSM1298009 c.19G>A p.E7K Substitution - Missense 11:36501497-36501497 - HCC8 COSM1604517 c.767A>G p.N256S Substitution - Missense 11:36490640-36490640 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.444172 11p12 602355

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C 3-UTRSNV . c.1566+2643T>G 11 36508748 HC A G Missense p.I223T c.668T>C 11 36516536 UCEC A G Missense p.L273S c.818T>C 11 36512139 CM A G Synonymous p.L140L c.418T>C 11 36520069 LUAD A T Missense p.N115K c.345T>A 11 36520142 STAD C A 3-UTRSNV . c.1566+2741G>T 11 36508650 HC C A Missense p.G521W c.1561G>T 11 36511396 STAD C A SpliceAcceptorSNV . c.448-1G>T 11 36518817 GBM C T 3-UTRSNV . c.1566+1437G>A 11 36509954 DLBCL C T Missense p.A481T c.1441G>A 11 36511516 OV C T Missense p.C242Y c.725G>A 11 36514132 LUSC C T Missense p.D120N c.358G>A 11 36520129 LUSC C T Missense p.E114K c.340G>A 11 36520147 CM C T Missense p.E291K c.871G>A 11 36512086 SCLC C T Missense p.E315K c.943G>A 11 36512014 STAD C T Missense p.E369K c.1105G>A 11 36511852 BRCA C T Missense p.E7K c.19G>A 11 36523047 BLCA C T Missense p.G383D c.1148G>A 11 36511809 HNSC C T Missense p.M414I c.1242G>A 11 36511715 LUSC C T Missense p.R305H c.914G>A 11 36512043 STAD C T Missense p.R392H c.1175G>A 11 36511782 BRCA C T Synonymous p.L364L c.1092G>A 11 36511865 STAD C T Synonymous p.R509R c.1527G>A 11 36511430 CM G A Missense p.H376Y c.1126C>T 11 36511831 CM G A Missense p.L409F c.1225C>T 11 36511732 CM G A Missense p.P241S c.721C>T 11 36514136 CM G A Missense p.P423L c.1268C>T 11 36511689 CM G A Missense p.R466W c.1396C>T 11 36511561 OV G A Missense p.S97L c.290C>T 11 36522776 LUSC G A Synonymous p.I203I c.609C>T 11 36516595 CM G A Synonymous p.L117L c.349C>T 11 36520138 ESCA G A Synonymous p.L422L c.1266C>T 11 36511691 CM G A Synonymous p.T336T c.1008C>T 11 36511949 LUAD G - Frameshift p.P239Qfs*32 c.716delC 11 36514141 RCCC G T Missense p.H300N c.898C>A 11 36512059 LUSC G T Missense p.R502S c.1504C>A 11 36511453 LUAD G T Synonymous p.P284P c.852C>A 11 36512105 CM T A Missense p.K489M c.1466A>T 11 36511491 LUAD T A Missense p.T336S c.1006A>T 11 36511951 SCLC T C Missense p.K171E c.511A>G 11 36518753 BRCA T C Missense p.N121S c.362A>G 11 36520125 ESCA T C Missense p.N212S c.635A>G 11 36516569 UCEC T C Missense p.Q186R c.557A>G 11 36518707 BRCA TGGACAATC - InFrameDeletion p.D181_P183delDCP c.541_549delGATTGTCCA 11 36518715 ESCA T G IntronicSNV . c.297-443A>C 11 36520633 PIA