Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 11 47256376 47256376 + Frame_Shift_Del DEL C C - TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chr11:47256376delC c.771delC c.(769-771)ttcfs p.F257fs BLCA 11 47236784 47236784 + Missense_Mutation SNP G G C TCGA-BT-A20R-01A-12D-A16O-08 TCGA-BT-A20R-11A-11D-A16O-08 g.chr11:47236784G>C c.97G>C c.(97-99)Gag>Cag p.E33Q BLCA 11 47236798 47236798 + Silent SNP C C G TCGA-GU-AATP-01A-11D-A391-08 TCGA-GU-AATP-10A-01D-A394-08 g.chr11:47236798C>G c.111C>G c.(109-111)ctC>ctG p.L37L BLCA 11 47237917 47237917 + Missense_Mutation SNP T T C TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr11:47237917T>C c.158T>C c.(157-159)cTc>cCc p.L53P BLCA 11 47254407 47254407 + Missense_Mutation SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr11:47254407C>T c.499C>T c.(499-501)Ctc>Ttc p.L167F BLCA 11 47254409 47254409 + Silent SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr11:47254409C>T c.501C>T c.(499-501)ctC>ctT p.L167L BLCA 11 47254498 47254498 + Nonsense_Mutation SNP C C G TCGA-CF-A47X-01A-31D-A23U-08 TCGA-CF-A47X-10A-01D-A23U-08 g.chr11:47254498C>G c.590C>G c.(589-591)tCa>tGa p.S197* BLCA 11 47254498 47254499 + Frame_Shift_Ins INS - - A TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr11:47254498_47254499insA c.590_591insA c.(589-594)tcagacfs p.D198fs BLCA 11 47256319 47256319 + Silent SNP C C T TCGA-FD-A5BS-01A-21D-A26M-08 TCGA-FD-A5BS-10A-01D-A26K-08 g.chr11:47256319C>T c.714C>T c.(712-714)ctC>ctT p.L238L BLCA 11 47256391 47256391 + Silent SNP C C G TCGA-E7-A85H-01A-11D-A34U-08 TCGA-E7-A85H-10B-01D-A34X-08 g.chr11:47256391C>G c.786C>G c.(784-786)tcC>tcG p.S262S BLCA 11 47256432 47256432 + Missense_Mutation SNP G G C TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr11:47256432G>C c.827G>C c.(826-828)aGa>aCa p.R276T BLCA 11 47256451 47256451 + Silent SNP C C T TCGA-CF-A47X-01A-31D-A23U-08 TCGA-CF-A47X-10A-01D-A23U-08 g.chr11:47256451C>T c.846C>T c.(844-846)ctC>ctT p.L282L BLCA 11 47256871 47256871 + Missense_Mutation SNP G G C TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr11:47256871G>C c.931G>C c.(931-933)Gag>Cag p.E311Q BLCA 11 47259414 47259414 + Silent SNP C C T TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr11:47259414C>T c.1050C>T c.(1048-1050)ctC>ctT p.L350L BLCA 11 47259489 47259489 + Silent SNP C C T TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr11:47259489C>T c.1125C>T c.(1123-1125)ttC>ttT p.F375F BLCA 11 47259519 47259519 + Silent SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr11:47259519G>A c.1155G>A c.(1153-1155)caG>caA p.Q385Q BLCA 11 47259526 47259526 + Missense_Mutation SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr11:47259526G>A c.1162G>A c.(1162-1164)Gac>Aac p.D388N BLCA 11 47260364 47260364 + Silent SNP C C T TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr11:47260364C>T c.1248C>T c.(1246-1248)ctC>ctT p.L416L BRCA 11 47237948 47237948 + Silent SNP G G A TCGA-A2-A3XT-01A-11D-A22X-09 TCGA-A2-A3XT-10A-01D-A22X-09 g.chr11:47237948G>A c.189G>A c.(187-189)ctG>ctA p.L63L BRCA 11 47254427 47254427 + Silent SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:47254427C>T c.519C>T c.(517-519)taC>taT p.Y173Y BRCA 11 47256321 47256321 + Missense_Mutation SNP G G A TCGA-GM-A2D9-01A-11D-A18P-09 TCGA-GM-A2D9-11A-42D-A18P-09 g.chr11:47256321G>A c.716G>A c.(715-717)aGa>aAa p.R239K BRCA 11 47259551 47259551 + Splice_Site SNP C C T TCGA-B6-A0IO-01A-11W-A050-09 TCGA-B6-A0IO-10A-01W-A055-09 g.chr11:47259551C>T c.1187C>T c.(1186-1188)tCg>tTg p.S396L CESC 11 47256412 47256412 + Missense_Mutation SNP T T G TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr11:47256412T>G c.807T>G c.(805-807)atT>atG p.I269M CESC 11 47256436 47256436 + Silent SNP G G T TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr11:47256436G>T c.831G>T c.(829-831)ggG>ggT p.G277G CHOL 11 47236765 47236765 + Missense_Mutation SNP T T G TCGA-ZU-A8S4-01A-11D-A417-09 TCGA-ZU-A8S4-10A-01D-A41A-09 g.chr11:47236765T>G c.78T>G c.(76-78)agT>agG p.S26R CHOL 11 47256385 47256385 + Silent SNP A A G TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr11:47256385A>G c.780A>G c.(778-780)acA>acG p.T260T CHOL 11 47256429 47256429 + Missense_Mutation SNP T T G TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr11:47256429T>G c.824T>G c.(823-825)gTt>gGt p.V275G COAD 11 47254445 47254445 + Silent SNP A A T TCGA-AA-A01K-01A-01W-A00E-09 TCGA-AA-A01K-10A-01W-A00E-09 g.chr11:47254445A>T c.537A>T c.(535-537)ggA>ggT p.G179G COADREAD 11 47254445 47254445 + Silent SNP A A T TCGA-AA-A01K-01A-01W-A00E-09 TCGA-AA-A01K-10A-01W-A00E-09 g.chr11:47254445A>T c.537A>T c.(535-537)ggA>ggT p.G179G COADREAD 11 47259489 47259489 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:47259489C>T c.1125C>T c.(1123-1125)ttC>ttT p.F375F COADREAD 11 47259490 47259490 + Missense_Mutation SNP G G A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:47259490G>A c.1126G>A c.(1126-1128)Gat>Aat p.D376N ESCA 11 47237962 47237962 + Missense_Mutation SNP G G A TCGA-L5-A88Z-01A-11D-A36J-09 TCGA-L5-A88Z-11A-11D-A36M-09 g.chr11:47237962G>A c.203G>A c.(202-204)aGc>aAc p.S68N ESCA 11 47254427 47254427 + Silent SNP C C T TCGA-L5-A8NH-01A-11D-A37C-09 TCGA-L5-A8NH-11A-11D-A37F-09 g.chr11:47254427C>T c.519C>T c.(517-519)taC>taT p.Y173Y GBM 11 47254492 47254492 + Missense_Mutation SNP C C T TCGA-06-2570-01A-01D-1495-08 TCGA-06-2570-10A-01D-1495-08 g.chr11:47254492C>T c.584C>T c.(583-585)gCc>gTc p.A195V GBMLGG 11 47254492 47254492 + Missense_Mutation SNP C C T TCGA-06-2570-01A-01D-1495-08 TCGA-06-2570-10A-01D-1495-08 g.chr11:47254492C>T c.584C>T c.(583-585)gCc>gTc p.A195V GBMLGG 11 47256422 47256422 + Missense_Mutation SNP C C T TCGA-DB-A4XA-01A-11D-A26M-08 TCGA-DB-A4XA-10A-01D-A26K-08 g.chr11:47256422C>T c.817C>T c.(817-819)Cgc>Tgc p.R273C GBMLGG 11 47256422 47256422 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:47256422C>T c.817C>T c.(817-819)Cgc>Tgc p.R273C HNSC 11 47256377 47256377 + Silent SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr11:47256377C>T c.772C>T c.(772-774)Ctg>Ttg p.L258L HNSC 11 47256422 47256422 + Missense_Mutation SNP C C T TCGA-CN-5361-01A-01D-1434-08 TCGA-CN-5361-10A-01D-1434-08 g.chr11:47256422C>T c.817C>T c.(817-819)Cgc>Tgc p.R273C HNSC 11 47256845 47256845 + Missense_Mutation SNP G G A TCGA-CV-5444-01A-02D-1512-08 TCGA-CV-5444-11A-01D-1512-08 g.chr11:47256845G>A c.905G>A c.(904-906)cGg>cAg p.R302Q HNSC 11 47259428 47259428 + Missense_Mutation SNP G G A TCGA-HD-8634-01A-11D-2394-08 TCGA-HD-8634-10A-01D-2394-08 g.chr11:47259428G>A c.1064G>A c.(1063-1065)cGa>cAa p.R355Q HNSC 11 47259551 47259551 + Splice_Site SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr11:47259551C>T c.1187C>T c.(1186-1188)tCg>tTg p.S396L LGG 11 47256422 47256422 + Missense_Mutation SNP C C T TCGA-DB-A4XA-01A-11D-A26M-08 TCGA-DB-A4XA-10A-01D-A26K-08 g.chr11:47256422C>T c.817C>T c.(817-819)Cgc>Tgc p.R273C LGG 11 47256422 47256422 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:47256422C>T c.817C>T c.(817-819)Cgc>Tgc p.R273C LIHC 11 47238448 47238448 + Missense_Mutation SNP C C T TCGA-DD-A39Z-01A-11D-A20W-10 TCGA-DD-A39Z-11A-21D-A20W-10 g.chr11:47238448C>T c.304C>T c.(304-306)Cgg>Tgg p.R102W LIHC 11 47238524 47238524 + Missense_Mutation SNP T T C TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr11:47238524T>C c.380T>C c.(379-381)gTg>gCg p.V127A LIHC 11 47259439 47259439 + Frame_Shift_Del DEL C C - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr11:47259439delC c.1075delC c.(1075-1077)cctfs p.P359fs LUAD 11 47256366 47256366 + Missense_Mutation SNP G G T TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr11:47256366G>T c.761G>T c.(760-762)tGt>tTt p.C254F LUAD 11 47256828 47256828 + Silent SNP C C T TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr11:47256828C>T c.888C>T c.(886-888)ttC>ttT p.F296F LUSC 11 47238436 47238436 + Missense_Mutation SNP C C G TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr11:47238436C>G c.292C>G c.(292-294)Ctg>Gtg p.L98V LUSC 11 47254483 47254483 + Missense_Mutation SNP G G T TCGA-18-3407-01A-01D-0983-08 TCGA-18-3407-11A-01D-0983-08 g.chr11:47254483G>T c.575G>T c.(574-576)cGa>cTa p.R192L LUSC 11 47259387 47259387 + Splice_Site SNP G G A TCGA-60-2722-01A-01D-1522-08 TCGA-60-2722-11A-01D-1522-08 g.chr11:47259387G>A c.e8-1 OV 11 47256952 47256952 + Missense_Mutation SNP A A C TCGA-13-0904-01A-02W-0420-08 TCGA-13-0904-10A-01D-0399-08 g.chr11:47256952A>C c.1012A>C c.(1012-1014)Aca>Cca p.T338P PAAD 11 47259552 47259552 + Splice_Site SNP G G A TCGA-RB-AA9M-01A-11D-A397-08 TCGA-RB-AA9M-10A-01D-A39A-08 g.chr11:47259552G>A c.1188G>A c.(1186-1188)tcG>tcA p.S396S READ 11 47259489 47259489 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:47259489C>T c.1125C>T c.(1123-1125)ttC>ttT p.F375F READ 11 47259490 47259490 + Missense_Mutation SNP G G A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:47259490G>A c.1126G>A c.(1126-1128)Gat>Aat p.D376N SARC 11 47236754 47236754 + Missense_Mutation SNP A A G TCGA-DX-AB2H-01A-11D-A38Z-09 TCGA-DX-AB2H-10A-01D-A38Z-09 g.chr11:47236754A>G c.67A>G c.(67-69)Agg>Ggg p.R23G SKCM 11 47256142 47256142 + Silent SNP G G C TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr11:47256142G>C c.621G>C c.(619-621)ctG>ctC p.L207L SKCM 11 47256474 47256474 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:47256474C>T c.869C>T c.(868-870)cCt>cTt p.P290L SKCM 11 47256923 47256923 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:47256923C>T c.983C>T c.(982-984)cCg>cTg p.P328L SKCM 11 47259440 47259440 + Missense_Mutation SNP C C T TCGA-D3-A1QA-06A-11D-A196-08 TCGA-D3-A1QA-10A-01D-A198-08 g.chr11:47259440C>T c.1076C>T c.(1075-1077)cCt>cTt p.P359L

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 47256321 47256321 single base substitution G A intron_variant BLCA-CN 11 47256321 47256321 single base substitution G A missense_variant R175K 524G>A BLCA-CN 11 47256321 47256321 single base substitution G A missense_variant R239K 716G>A BLCA-US 11 47236784 47236784 single base substitution G C missense_variant E33Q 97G>C BLCA-US 11 47237917 47237917 single base substitution T C missense_variant L53P 158T>C BLCA-US 11 47254407 47254407 single base substitution C T intron_variant BLCA-US 11 47254407 47254407 single base substitution C T missense_variant L103F 307C>T BLCA-US 11 47254407 47254407 single base substitution C T missense_variant L167F 499C>T BLCA-US 11 47254409 47254409 single base substitution C T intron_variant BLCA-US 11 47254409 47254409 single base substitution C T synonymous_variant L103L 309C>T BLCA-US 11 47254409 47254409 single base substitution C T synonymous_variant L167L 501C>T BLCA-US 11 47259519 47259519 single base substitution G A 3_prime_UTR_variant BLCA-US 11 47259519 47259519 single base substitution G A synonymous_variant Q196Q 588G>A BLCA-US 11 47259519 47259519 single base substitution G A synonymous_variant Q321Q 963G>A BLCA-US 11 47259519 47259519 single base substitution G A synonymous_variant Q385Q 1155G>A BLCA-US 11 47259526 47259526 single base substitution G A 3_prime_UTR_variant BLCA-US 11 47259526 47259526 single base substitution G A missense_variant D199N 595G>A BLCA-US 11 47259526 47259526 single base substitution G A missense_variant D324N 970G>A BLCA-US 11 47259526 47259526 single base substitution G A missense_variant D388N 1162G>A BRCA-EU 11 47233222 47233222 single base substitution C T upstream_gene_variant BRCA-EU 11 47233587 47233587 single base substitution C G upstream_gene_variant BRCA-EU 11 47233665 47233665 single base substitution G T upstream_gene_variant BRCA-EU 11 47234039 47234039 single base substitution G A upstream_gene_variant BRCA-EU 11 47235851 47235851 single base substitution G C upstream_gene_variant BRCA-EU 11 47236283 47236283 single base substitution C G upstream_gene_variant BRCA-EU 11 47239442 47239442 deletion of <=200bp A - intron_variant BRCA-EU 11 47239525 47239525 single base substitution A G intron_variant BRCA-EU 11 47242031 47242031 single base substitution G A intron_variant BRCA-EU 11 47244108 47244108 single base substitution G C intron_variant BRCA-EU 11 47246015 47246015 single base substitution G C intron_variant BRCA-EU 11 47248991 47248991 insertion of <=200bp - A intron_variant BRCA-EU 11 47249493 47249493 single base substitution C T intron_variant BRCA-EU 11 47250322 47250336 deletion of <=200bp ACATGATGAAACTCC - intron_variant BRCA-EU 11 47251960 47251960 single base substitution G A intron_variant BRCA-EU 11 47254034 47254034 single base substitution C G intron_variant BRCA-EU 11 47255990 47255990 single base substitution G C intron_variant BRCA-EU 11 47257300 47257300 single base substitution T G intron_variant BRCA-EU 11 47257393 47257393 single base substitution G A intron_variant BRCA-EU 11 47258117 47258117 single base substitution A C intron_variant BRCA-EU 11 47259539 47259539 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 47259539 47259539 single base substitution C G missense_variant S203C 608C>G BRCA-EU 11 47259539 47259539 single base substitution C G missense_variant S328C 983C>G BRCA-EU 11 47259539 47259539 single base substitution C G missense_variant S392C 1175C>G BRCA-EU 11 47259938 47259938 single base substitution C G intron_variant BRCA-EU 11 47260763 47260763 single base substitution G T 3_prime_UTR_variant BRCA-EU 11 47260817 47260817 single base substitution G A downstream_gene_variant BRCA-EU 11 47261176 47261176 single base substitution G A downstream_gene_variant BRCA-EU 11 47262529 47262529 single base substitution C T downstream_gene_variant BRCA-EU 11 47263478 47263478 single base substitution T C downstream_gene_variant BRCA-EU 11 47265098 47265098 single base substitution C G downstream_gene_variant BRCA-EU 11 47265146 47265146 single base substitution G A downstream_gene_variant BRCA-FR 11 47233665 47233665 single base substitution G T upstream_gene_variant BRCA-FR 11 47243612 47243612 single base substitution C T intron_variant BRCA-FR 11 47251887 47251887 single base substitution G A intron_variant BRCA-FR 11 47253265 47253265 single base substitution C G intron_variant BRCA-FR 11 47254034 47254034 single base substitution C G intron_variant BRCA-FR 11 47259539 47259539 single base substitution C G 3_prime_UTR_variant BRCA-FR 11 47259539 47259539 single base substitution C G missense_variant S203C 608C>G BRCA-FR 11 47259539 47259539 single base substitution C G missense_variant S328C 983C>G BRCA-FR 11 47259539 47259539 single base substitution C G missense_variant S392C 1175C>G BRCA-FR 11 47265098 47265098 single base substitution C G downstream_gene_variant BRCA-UK 11 47234039 47234039 single base substitution G A upstream_gene_variant BRCA-UK 11 47252620 47252620 single base substitution G A intron_variant BRCA-UK 11 47264624 47264624 single base substitution C T downstream_gene_variant BRCA-US 11 47237948 47237948 single base substitution G A synonymous_variant L63L 189G>A BRCA-US 11 47254427 47254427 single base substitution C T intron_variant BRCA-US 11 47254427 47254427 single base substitution C T synonymous_variant Y109Y 327C>T BRCA-US 11 47254427 47254427 single base substitution C T synonymous_variant Y173Y 519C>T BRCA-US 11 47256321 47256321 single base substitution G A intron_variant BRCA-US 11 47256321 47256321 single base substitution G A missense_variant R175K 524G>A BRCA-US 11 47256321 47256321 single base substitution G A missense_variant R239K 716G>A BRCA-US 11 47259551 47259551 single base substitution C T missense_variant S207L 620C>T BRCA-US 11 47259551 47259551 single base substitution C T missense_variant S332L 995C>T BRCA-US 11 47259551 47259551 single base substitution C T missense_variant S396L 1187C>T BRCA-US 11 47259551 47259551 single base substitution C T splice_region_variant BTCA-JP 11 47251369 47251369 single base substitution C T intron_variant BTCA-JP 11 47264345 47264345 single base substitution C T downstream_gene_variant CESC-US 11 47242214 47242214 single base substitution G C intron_variant CESC-US 11 47242251 47242251 single base substitution G T intron_variant CESC-US 11 47256412 47256412 single base substitution T G intron_variant CESC-US 11 47256412 47256412 single base substitution T G missense_variant I205M 615T>G CESC-US 11 47256412 47256412 single base substitution T G missense_variant I269M 807T>G CESC-US 11 47256436 47256436 single base substitution G T intron_variant CESC-US 11 47256436 47256436 single base substitution G T synonymous_variant G213G 639G>T CESC-US 11 47256436 47256436 single base substitution G T synonymous_variant G277G 831G>T CLLE-ES 11 47259983 47259983 single base substitution C T intron_variant COAD-US 11 47264653 47264653 deletion of <=200bp A - downstream_gene_variant COCA-CN 11 47250536 47250536 single base substitution C A intron_variant COCA-CN 11 47251652 47251652 single base substitution T C intron_variant COCA-CN 11 47254562 47254562 single base substitution C T intron_variant COCA-CN 11 47256963 47256963 single base substitution G T intron_variant COCA-CN 11 47256963 47256963 single base substitution G T missense_variant K277N 831G>T COCA-CN 11 47256963 47256963 single base substitution G T missense_variant K341N 1023G>T COCA-CN 11 47256963 47256963 single base substitution G T splice_region_variant COCA-CN 11 47259542 47259542 single base substitution G A 3_prime_UTR_variant COCA-CN 11 47259542 47259542 single base substitution G A missense_variant G204D 611G>A COCA-CN 11 47259542 47259542 single base substitution G A missense_variant G329D 986G>A COCA-CN 11 47259542 47259542 single base substitution G A missense_variant G393D 1178G>A COCA-CN 11 47260289 47260289 single base substitution G A intron_variant COCA-CN 11 47262165 47262165 single base substitution G A downstream_gene_variant COCA-CN 11 47263457 47263457 single base substitution A G downstream_gene_variant ESAD-UK 11 47231608 47231608 single base substitution C G upstream_gene_variant ESAD-UK 11 47231765 47231765 single base substitution C A upstream_gene_variant ESAD-UK 11 47232536 47232536 single base substitution T G upstream_gene_variant ESAD-UK 11 47234196 47234196 single base substitution T C upstream_gene_variant ESAD-UK 11 47238851 47238851 single base substitution C T intron_variant ESAD-UK 11 47240492 47240492 single base substitution C T intron_variant ESAD-UK 11 47241058 47241058 single base substitution C T intron_variant ESAD-UK 11 47241166 47241166 single base substitution G T intron_variant ESAD-UK 11 47242949 47242949 single base substitution C T intron_variant ESAD-UK 11 47243184 47243184 single base substitution C T intron_variant ESAD-UK 11 47244929 47244929 single base substitution G A intron_variant ESAD-UK 11 47245047 47245047 insertion of <=200bp - TAAC intron_variant ESAD-UK 11 47245493 47245493 deletion of <=200bp A - intron_variant ESAD-UK 11 47245579 47245579 single base substitution G A intron_variant ESAD-UK 11 47245624 47245624 single base substitution A T intron_variant ESAD-UK 11 47246374 47246374 single base substitution C T intron_variant ESAD-UK 11 47246932 47246932 single base substitution A G intron_variant ESAD-UK 11 47248038 47248038 single base substitution G A intron_variant ESAD-UK 11 47248909 47248909 single base substitution C T intron_variant ESAD-UK 11 47253075 47253075 single base substitution T A intron_variant ESAD-UK 11 47253412 47253412 single base substitution G A intron_variant ESAD-UK 11 47253809 47253809 single base substitution C T intron_variant ESAD-UK 11 47255654 47255654 deletion of <=200bp T - intron_variant ESAD-UK 11 47256104 47256104 single base substitution A T intron_variant ESAD-UK 11 47256990 47256992 deletion of <=200bp AGA - intron_variant ESAD-UK 11 47257632 47257632 single base substitution C T intron_variant ESAD-UK 11 47262508 47262508 single base substitution A G downstream_gene_variant ESAD-UK 11 47262962 47262962 single base substitution G A downstream_gene_variant ESAD-UK 11 47263935 47263935 single base substitution C T downstream_gene_variant GBM-US 11 47254492 47254492 single base substitution C T intron_variant GBM-US 11 47254492 47254492 single base substitution C T missense_variant A131V 392C>T GBM-US 11 47254492 47254492 single base substitution C T missense_variant A195V 584C>T LAML-KR 11 47242952 47242952 single base substitution G A intron_variant LAML-KR 11 47251387 47251387 single base substitution C T intron_variant LAML-KR 11 47254615 47254615 single base substitution A G intron_variant LAML-KR 11 47256462 47256462 single base substitution C T intron_variant LAML-KR 11 47256462 47256462 single base substitution C T missense_variant P222L 665C>T LAML-KR 11 47256462 47256462 single base substitution C T missense_variant P286L 857C>T LGG-US 11 47256422 47256422 single base substitution C T intron_variant LGG-US 11 47256422 47256422 single base substitution C T missense_variant R209C 625C>T LGG-US 11 47256422 47256422 single base substitution C T missense_variant R273C 817C>T LGG-US 11 47264838 47264838 single base substitution G A downstream_gene_variant LICA-FR 11 47257501 47257501 single base substitution C T intron_variant LICA-FR 11 47260711 47260711 single base substitution A C 3_prime_UTR_variant LIHC-US 11 47256456 47256456 single base substitution C A intron_variant LIHC-US 11 47256456 47256456 single base substitution C A stop_gained S220* 659C>A LIHC-US 11 47256456 47256456 single base substitution C A stop_gained S284* 851C>A LIHC-US 11 47260382 47260382 single base substitution A G 3_prime_UTR_variant LIHC-US 11 47260382 47260382 single base substitution A G synonymous_variant E233E 699A>G LIHC-US 11 47260382 47260382 single base substitution A G synonymous_variant E358E 1074A>G LIHC-US 11 47260382 47260382 single base substitution A G synonymous_variant E422E 1266A>G LINC-JP 11 47246074 47246074 single base substitution T C intron_variant LINC-JP 11 47251190 47251190 single base substitution G A intron_variant LINC-JP 11 47251387 47251387 single base substitution C T intron_variant LINC-JP 11 47255635 47255635 single base substitution A G intron_variant LINC-JP 11 47256053 47256053 single base substitution G T intron_variant LINC-JP 11 47259162 47259162 single base substitution A G intron_variant LINC-JP 11 47264698 47264698 single base substitution G A downstream_gene_variant LIRI-JP 11 47233655 47233655 single base substitution C T upstream_gene_variant LIRI-JP 11 47234089 47234089 single base substitution T C upstream_gene_variant LIRI-JP 11 47234178 47234178 single base substitution T C upstream_gene_variant LIRI-JP 11 47234509 47234509 single base substitution G A upstream_gene_variant LIRI-JP 11 47234749 47234749 single base substitution C A upstream_gene_variant LIRI-JP 11 47234801 47234801 single base substitution C A upstream_gene_variant LIRI-JP 11 47235046 47235046 single base substitution A G upstream_gene_variant LIRI-JP 11 47235107 47235107 single base substitution G A upstream_gene_variant LIRI-JP 11 47237230 47237230 single base substitution G T intron_variant LIRI-JP 11 47240712 47240712 single base substitution T C intron_variant LIRI-JP 11 47243692 47243692 single base substitution C T intron_variant LIRI-JP 11 47245201 47245201 single base substitution T C intron_variant LIRI-JP 11 47251129 47251129 single base substitution T C intron_variant LIRI-JP 11 47254204 47254204 single base substitution A C intron_variant LIRI-JP 11 47256398 47256401 deletion of <=200bp CAAA - frameshift_variant QT201 LIRI-JP 11 47256398 47256401 deletion of <=200bp CAAA - frameshift_variant QT265 LIRI-JP 11 47256398 47256401 deletion of <=200bp CAAA - intron_variant LIRI-JP 11 47257862 47257862 single base substitution T C intron_variant LIRI-JP 11 47260293 47260293 single base substitution C A intron_variant LIRI-JP 11 47261745 47261745 insertion of <=200bp - C downstream_gene_variant LIRI-JP 11 47261871 47261871 single base substitution T C downstream_gene_variant LIRI-JP 11 47264848 47264848 single base substitution T A downstream_gene_variant LIRI-JP 11 47264853 47264853 single base substitution T C downstream_gene_variant LIRI-JP 11 47265696 47265696 single base substitution T C downstream_gene_variant LUSC-KR 11 47235496 47235496 single base substitution G T upstream_gene_variant LUSC-KR 11 47236199 47236199 single base substitution G T upstream_gene_variant LUSC-KR 11 47236614 47236614 single base substitution C T 5_prime_UTR_variant LUSC-KR 11 47240309 47240309 single base substitution G T intron_variant LUSC-KR 11 47243612 47243612 single base substitution C T intron_variant LUSC-KR 11 47244768 47244768 single base substitution G A intron_variant LUSC-KR 11 47249624 47249624 single base substitution G A intron_variant LUSC-KR 11 47251520 47251520 single base substitution C T intron_variant LUSC-KR 11 47258309 47258309 single base substitution A T intron_variant LUSC-US 11 47238436 47238436 single base substitution C G intron_variant LUSC-US 11 47238436 47238436 single base substitution C G missense_variant L98V 292C>G LUSC-US 11 47254483 47254483 single base substitution G T intron_variant LUSC-US 11 47254483 47254483 single base substitution G T missense_variant R128L 383G>T LUSC-US 11 47254483 47254483 single base substitution G T missense_variant R192L 575G>T LUSC-US 11 47259387 47259387 single base substitution G A splice_acceptor_variant MALY-DE 11 47237989 47237989 single base substitution A C missense_variant K77T 230A>C MALY-DE 11 47240212 47240212 single base substitution C T intron_variant MALY-DE 11 47242615 47242615 single base substitution G C intron_variant MALY-DE 11 47247189 47247189 single base substitution A G intron_variant MALY-DE 11 47247565 47247565 single base substitution A C intron_variant MALY-DE 11 47250530 47250530 single base substitution A C intron_variant MALY-DE 11 47250570 47250570 single base substitution A T intron_variant MALY-DE 11 47250627 47250627 single base substitution T C intron_variant MALY-DE 11 47250659 47250659 single base substitution T C intron_variant MALY-DE 11 47253075 47253075 single base substitution T A intron_variant MALY-DE 11 47259149 47259149 insertion of <=200bp - T intron_variant MELA-AU 11 47231561 47231561 single base substitution C T upstream_gene_variant MELA-AU 11 47231789 47231789 single base substitution C T upstream_gene_variant MELA-AU 11 47232814 47232814 single base substitution G A upstream_gene_variant MELA-AU 11 47232999 47232999 single base substitution C T upstream_gene_variant MELA-AU 11 47233079 47233079 single base substitution C T upstream_gene_variant MELA-AU 11 47234367 47234367 single base substitution C T upstream_gene_variant MELA-AU 11 47234495 47234496 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 47235059 47235059 single base substitution C A upstream_gene_variant MELA-AU 11 47235188 47235188 single base substitution G A upstream_gene_variant MELA-AU 11 47236442 47236442 single base substitution C T upstream_gene_variant MELA-AU 11 47236456 47236456 single base substitution C T upstream_gene_variant MELA-AU 11 47236495 47236495 single base substitution C T 5_prime_UTR_variant MELA-AU 11 47237554 47237554 single base substitution C T intron_variant MELA-AU 11 47237636 47237636 single base substitution G A intron_variant MELA-AU 11 47238671 47238671 single base substitution A G intron_variant MELA-AU 11 47239154 47239154 single base substitution C T intron_variant MELA-AU 11 47239365 47239366 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 47239366 47239366 single base substitution C T intron_variant MELA-AU 11 47239389 47239389 single base substitution C T intron_variant MELA-AU 11 47239702 47239702 single base substitution C T intron_variant MELA-AU 11 47239705 47239705 single base substitution C T intron_variant MELA-AU 11 47240978 47240978 single base substitution C T intron_variant MELA-AU 11 47241813 47241813 single base substitution C T intron_variant MELA-AU 11 47243174 47243174 single base substitution T C intron_variant MELA-AU 11 47244075 47244075 single base substitution T C intron_variant MELA-AU 11 47244839 47244839 single base substitution C T intron_variant MELA-AU 11 47245395 47245395 single base substitution C T intron_variant MELA-AU 11 47245455 47245455 single base substitution A G intron_variant MELA-AU 11 47245481 47245482 multiple base substitution (>=2bp and <=200bp) CC TA intron_variant MELA-AU 11 47247671 47247671 single base substitution T A intron_variant MELA-AU 11 47248004 47248004 single base substitution C T intron_variant MELA-AU 11 47248146 47248146 single base substitution C T intron_variant MELA-AU 11 47248180 47248180 single base substitution T C intron_variant MELA-AU 11 47248774 47248774 single base substitution C T intron_variant MELA-AU 11 47248883 47248883 single base substitution C T intron_variant MELA-AU 11 47249863 47249863 single base substitution C T intron_variant MELA-AU 11 47250078 47250078 single base substitution C T intron_variant MELA-AU 11 47250333 47250333 single base substitution C T intron_variant MELA-AU 11 47251832 47251832 single base substitution C T intron_variant MELA-AU 11 47251851 47251851 single base substitution C A intron_variant MELA-AU 11 47253617 47253617 single base substitution G A intron_variant MELA-AU 11 47254174 47254174 single base substitution A G intron_variant MELA-AU 11 47254266 47254266 single base substitution C T intron_variant MELA-AU 11 47254419 47254419 single base substitution C T intron_variant MELA-AU 11 47254419 47254419 single base substitution C T stop_gained Q107* 319C>T MELA-AU 11 47254419 47254419 single base substitution C T stop_gained Q171* 511C>T MELA-AU 11 47254986 47254986 single base substitution G A intron_variant MELA-AU 11 47255060 47255060 single base substitution C T intron_variant MELA-AU 11 47255332 47255332 single base substitution C T intron_variant MELA-AU 11 47255661 47255661 single base substitution C T intron_variant MELA-AU 11 47255855 47255855 single base substitution T A intron_variant MELA-AU 11 47256131 47256131 single base substitution T C intron_variant MELA-AU 11 47256131 47256131 single base substitution T C missense_variant F140L 418T>C MELA-AU 11 47256131 47256131 single base substitution T C missense_variant F204L 610T>C MELA-AU 11 47257721 47257721 single base substitution C T intron_variant MELA-AU 11 47258057 47258058 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 47259261 47259261 single base substitution C A intron_variant MELA-AU 11 47259938 47259938 single base substitution C T intron_variant MELA-AU 11 47260547 47260547 single base substitution G A 3_prime_UTR_variant MELA-AU 11 47260891 47260891 single base substitution G A downstream_gene_variant MELA-AU 11 47262844 47262844 single base substitution G A downstream_gene_variant MELA-AU 11 47264404 47264404 single base substitution G A downstream_gene_variant MELA-AU 11 47264777 47264777 single base substitution C T downstream_gene_variant ORCA-IN 11 47235630 47235630 single base substitution T G upstream_gene_variant ORCA-IN 11 47247967 47247967 single base substitution G T intron_variant ORCA-IN 11 47255204 47255204 single base substitution G A intron_variant ORCA-IN 11 47256291 47256291 single base substitution C T intron_variant ORCA-IN 11 47256432 47256432 single base substitution G A intron_variant ORCA-IN 11 47256432 47256432 single base substitution G A missense_variant R212K 635G>A ORCA-IN 11 47256432 47256432 single base substitution G A missense_variant R276K 827G>A OV-AU 11 47232750 47232750 single base substitution G A upstream_gene_variant OV-AU 11 47246675 47246675 single base substitution G C intron_variant OV-AU 11 47248522 47248522 single base substitution A T intron_variant OV-AU 11 47248563 47248563 single base substitution C T intron_variant OV-AU 11 47255394 47255394 single base substitution C T intron_variant OV-AU 11 47258836 47258836 single base substitution G A intron_variant OV-AU 11 47259138 47259138 single base substitution C T intron_variant OV-AU 11 47265666 47265666 single base substitution T C downstream_gene_variant PACA-AU 11 47233271 47233271 single base substitution A G upstream_gene_variant PACA-AU 11 47234574 47234574 single base substitution T C upstream_gene_variant PACA-AU 11 47243007 47243007 deletion of <=200bp T - intron_variant PACA-AU 11 47245445 47245445 single base substitution C T intron_variant PACA-AU 11 47245809 47245809 single base substitution C T intron_variant PACA-AU 11 47245997 47245997 single base substitution C T intron_variant PACA-AU 11 47246042 47246042 single base substitution C T intron_variant PACA-AU 11 47246109 47246109 single base substitution C G intron_variant PACA-AU 11 47246280 47246280 single base substitution C G intron_variant PACA-AU 11 47246323 47246323 single base substitution C A intron_variant PACA-AU 11 47246598 47246598 single base substitution C A intron_variant PACA-AU 11 47246607 47246607 single base substitution C T intron_variant PACA-AU 11 47246613 47246613 single base substitution C T intron_variant PACA-AU 11 47250775 47250775 single base substitution T C intron_variant PACA-AU 11 47259384 47259384 single base substitution C G splice_region_variant PACA-AU 11 47264006 47264006 single base substitution C T downstream_gene_variant PACA-AU 11 47265521 47265523 deletion of <=200bp CTA - downstream_gene_variant PACA-CA 11 47234878 47234878 single base substitution A G upstream_gene_variant PACA-CA 11 47236155 47236155 single base substitution G A upstream_gene_variant PACA-CA 11 47244125 47244125 single base substitution G A intron_variant PACA-CA 11 47245004 47245004 single base substitution A G intron_variant PACA-CA 11 47245347 47245347 single base substitution T G intron_variant PACA-CA 11 47246446 47246446 insertion of <=200bp - T intron_variant PACA-CA 11 47253175 47253175 single base substitution G A intron_variant PACA-CA 11 47257190 47257190 insertion of <=200bp - T intron_variant PACA-CA 11 47258177 47258177 single base substitution T C intron_variant PACA-CA 11 47261100 47261100 single base substitution G A downstream_gene_variant PACA-CA 11 47262400 47262400 single base substitution G C downstream_gene_variant PACA-CA 11 47264106 47264106 single base substitution A G downstream_gene_variant PACA-CA 11 47264380 47264380 single base substitution G C downstream_gene_variant PAEN-AU 11 47245523 47245523 single base substitution G A intron_variant PAEN-AU 11 47253420 47253420 single base substitution G C intron_variant PAEN-IT 11 47239611 47239611 single base substitution C G intron_variant PBCA-DE 11 47235411 47235411 single base substitution T A upstream_gene_variant PBCA-DE 11 47245087 47245087 single base substitution T C intron_variant PRAD-CA 11 47245059 47245059 single base substitution C T intron_variant PRAD-UK 11 47241407 47241407 single base substitution C T intron_variant PRAD-UK 11 47245284 47245284 single base substitution G C intron_variant READ-US 11 47259700 47259700 single base substitution C A 3_prime_UTR_variant READ-US 11 47259700 47259700 single base substitution C A missense_variant F211L 633C>A READ-US 11 47259700 47259700 single base substitution C A missense_variant F336L 1008C>A READ-US 11 47259700 47259700 single base substitution C A missense_variant F400L 1200C>A RECA-EU 11 47234834 47234834 single base substitution C A upstream_gene_variant RECA-EU 11 47237474 47237474 single base substitution C A intron_variant RECA-EU 11 47259708 47259708 single base substitution T C 3_prime_UTR_variant RECA-EU 11 47259708 47259708 single base substitution T C missense_variant M214T 641T>C RECA-EU 11 47259708 47259708 single base substitution T C missense_variant M339T 1016T>C RECA-EU 11 47259708 47259708 single base substitution T C missense_variant M403T 1208T>C SKCA-BR 11 47233454 47233454 single base substitution A G upstream_gene_variant SKCA-BR 11 47236411 47236411 single base substitution T C upstream_gene_variant SKCA-BR 11 47236455 47236455 single base substitution C T upstream_gene_variant SKCA-BR 11 47239316 47239316 single base substitution C T intron_variant SKCA-BR 11 47246164 47246164 single base substitution G A intron_variant SKCA-BR 11 47246985 47246985 single base substitution C T intron_variant SKCA-BR 11 47253311 47253311 single base substitution T C intron_variant SKCA-BR 11 47261260 47261260 single base substitution G A downstream_gene_variant SKCM-US 11 47256474 47256474 single base substitution C T intron_variant SKCM-US 11 47256474 47256474 single base substitution C T missense_variant P226L 677C>T SKCM-US 11 47256474 47256474 single base substitution C T missense_variant P290L 869C>T SKCM-US 11 47256923 47256923 single base substitution C T 3_prime_UTR_variant SKCM-US 11 47256923 47256923 single base substitution C T intron_variant SKCM-US 11 47256923 47256923 single base substitution C T missense_variant P264L 791C>T SKCM-US 11 47256923 47256923 single base substitution C T missense_variant P328L 983C>T SKCM-US 11 47259440 47259440 single base substitution C T 3_prime_UTR_variant SKCM-US 11 47259440 47259440 single base substitution C T missense_variant P170L 509C>T SKCM-US 11 47259440 47259440 single base substitution C T missense_variant P295L 884C>T SKCM-US 11 47259440 47259440 single base substitution C T missense_variant P359L 1076C>T SKCM-US 11 47264356 47264356 single base substitution C T downstream_gene_variant SKCM-US 11 47264422 47264422 single base substitution C T downstream_gene_variant STAD-US 11 47238526 47238526 single base substitution G A intron_variant STAD-US 11 47238526 47238526 single base substitution G A missense_variant A128T 382G>A STAD-US 11 47256210 47256210 single base substitution T C intron_variant STAD-US 11 47256210 47256210 single base substitution T C missense_variant M166T 497T>C STAD-US 11 47256210 47256210 single base substitution T C missense_variant M230T 689T>C STAD-US 11 47264443 47264443 single base substitution G A downstream_gene_variant STAD-US 11 47264672 47264672 single base substitution C T downstream_gene_variant UCEC-US 11 47254483 47254483 single base substitution G A intron_variant UCEC-US 11 47254483 47254483 single base substitution G A missense_variant R128Q 383G>A UCEC-US 11 47254483 47254483 single base substitution G A missense_variant R192Q 575G>A UCEC-US 11 47256408 47256408 single base substitution A C intron_variant UCEC-US 11 47256408 47256408 single base substitution A C missense_variant K204T 611A>C UCEC-US 11 47256408 47256408 single base substitution A C missense_variant K268T 803A>C UCEC-US 11 47256905 47256905 single base substitution G T 3_prime_UTR_variant UCEC-US 11 47256905 47256905 single base substitution G T intron_variant UCEC-US 11 47256905 47256905 single base substitution G T missense_variant C258F 773G>T UCEC-US 11 47256905 47256905 single base substitution G T missense_variant C322F 965G>T UCEC-US 11 47259476 47259476 single base substitution C T 3_prime_UTR_variant UCEC-US 11 47259476 47259476 single base substitution C T missense_variant T182M 545C>T UCEC-US 11 47259476 47259476 single base substitution C T missense_variant T307M 920C>T UCEC-US 11 47259476 47259476 single base substitution C T missense_variant T371M 1112C>T UCEC-US 11 47259480 47259480 single base substitution C T 3_prime_UTR_variant UCEC-US 11 47259480 47259480 single base substitution C T synonymous_variant I183I 549C>T UCEC-US 11 47259480 47259480 single base substitution C T synonymous_variant I308I 924C>T UCEC-US 11 47259480 47259480 single base substitution C T synonymous_variant I372I 1116C>T UCEC-US 11 47259499 47259499 single base substitution T C 3_prime_UTR_variant UCEC-US 11 47259499 47259499 single base substitution T C missense_variant S190P 568T>C UCEC-US 11 47259499 47259499 single base substitution T C missense_variant S315P 943T>C UCEC-US 11 47259499 47259499 single base substitution T C missense_variant S379P 1135T>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PD2194a COSM27597 c.462_463delAG p.A155fs*10 Deletion - Frameshift 11:47232819-47232820 + C086 COSM5529622 c.684G>A p.L228L Substitution - coding silent 11:47234654-47234654 + TCGA-G2-A2EO-01 COSM1298087 c.499C>T p.L167F Substitution - Missense 11:47232856-47232856 + B105-0 COSM1746268 c.716G>A p.R239K Substitution - Missense 11:47234770-47234770 + ESCC_3 COSM5622541 c.1136C>G p.S379* Substitution - Nonsense 11:47237949-47237949 + TCGA-FW-A3R5-06 COSM3869221 c.983C>T p.P328L Substitution - Missense 11:47235372-47235372 + TCGA-WS-AB45-01 COSM1981291 c.265-7G>A p.? Unknown 11:47216851-47216851 + AD51 COSM5966573 c.737C>T p.T246M Substitution - Missense 11:47234791-47234791 + CN-AML-NR-34-Dx COSM5424286 c.857C>T p.P286L Substitution - Missense 11:47234911-47234911 + TCGA-BS-A0UF-01 COSM927369 c.1112C>T p.T371M Substitution - Missense 11:47237925-47237925 + CSCC-20-T COSM4448725 c.1208delT p.M403fs*>25 Deletion - Frameshift 11:47238157-47238157 + TCGA-HU-A4G8-01 COSM4033132 c.689T>C p.M230T Substitution - Missense 11:47234659-47234659 + TCGA-D5-6530-01 COSM5162151 c.1098T>C p.P366P Substitution - coding silent 11:47237911-47237911 + C086 COSM5529621 c.326C>T p.P109L Substitution - Missense 11:47216919-47216919 + T276 COSM4676656 c.231G>A p.K77K Substitution - coding silent 11:47216439-47216439 + S10-24679-TP COSM927370 c.1116C>T p.I372I Substitution - coding silent 11:47237929-47237929 + TCGA-60-2722-01 COSM687992 c.1024-1G>A p.? Unknown 11:47237836-47237836 + LOVO COSM1981294 c.379G>A p.V127M Substitution - Missense 11:47216972-47216972 + TCGA-AG-3892-01 COSM256744 c.1126G>A p.D376N Substitution - Missense 11:47237939-47237939 + LUAD-74TBW COSM354985 c.293T>C p.L98P Substitution - Missense 11:47216886-47216886 + TCGA-BR-4256-01 COSM4033131 c.382G>A p.A128T Substitution - Missense 11:47216975-47216975 + I2L-P19Ta-Tumor-Organoid COSM5360648 c.587G>A p.S196N Substitution - Missense 11:47232944-47232944 + TCGA-AA-A01K-01 COSM299932 c.537A>T p.G179G Substitution - coding silent 11:47232894-47232894 + TCGA-46-3769-01 COSM687995 c.292C>G p.L98V Substitution - Missense 11:47216885-47216885 + 8031544 COSM3383497 c.1024-4C>G p.? Unknown 11:47237833-47237833 + TCGA-06-2570-01 COSM3397717 c.584C>T p.A195V Substitution - Missense 11:47232941-47232941 + sysucc-880T COSM5461981 c.1178G>A p.G393D Substitution - Missense 11:47237991-47237991 + UMC11 COSM1981301 c.901G>A p.A301T Substitution - Missense 11:47235290-47235290 + TCGA-DK-A3WW-01 COSM3791522 c.1155G>A p.Q385Q Substitution - coding silent 11:47237968-47237968 + TCGA-FU-A3HZ-01 COSM4840623 c.807T>G p.I269M Substitution - Missense 11:47234861-47234861 + CSCC-27-T COSM4515270 c.1015_1016CC>TT p.P339F Substitution - Missense 11:47235404-47235405 + TCGA-G2-A2EO-01 COSM1298088 c.501C>T p.L167L Substitution - coding silent 11:47232858-47232858 + TCGA-AN-A046-01 COSM3809304 c.519C>T p.Y173Y Substitution - coding silent 11:47232876-47232876 + ESO-114 COSM1249843 c.210C>T p.V70V Substitution - coding silent 11:47216418-47216418 + PD3450a COSM30403 c.213G>A p.R71R Substitution - coding silent 11:47216421-47216421 + TCGA-BT-A20R-01 COSM1298085 c.97G>C p.E33Q Substitution - Missense 11:47215233-47215233 + SC_9047 COSM5560820 c.601A>G p.N201D Substitution - Missense 11:47232958-47232958 + TCGA-AP-A051-01 COSM927369 c.1112C>T p.T371M Substitution - Missense 11:47237925-47237925 + Pat_16_B COSM5838640 c.746C>T p.A249V Substitution - Missense 11:47234800-47234800 + PT41 COSM5924533 c.713T>A p.L238H Substitution - Missense 11:47234767-47234767 + U2940 COSM5620634 c.164T>C p.V55A Substitution - Missense 11:47216372-47216372 + TCGA-AP-A0LE-01 COSM927371 c.1135T>C p.S379P Substitution - Missense 11:47237948-47237948 + TCGA-DB-A4XA-01 COSM3967534 c.817C>T p.R273C Substitution - Missense 11:47234871-47234871 + TCGA-A2-A3XT-01 COSM3809303 c.189G>A p.L63L Substitution - coding silent 11:47216397-47216397 + pfg054T COSM4747161 c.728_729delAG p.K244fs*11 Deletion - Frameshift 11:47234782-47234783 + CN-AML-NR-19-Dx COSM5424286 c.857C>T p.P286L Substitution - Missense 11:47234911-47234911 + ME100L COSM231246 c.868C>T p.P290S Substitution - Missense 11:47234922-47234922 + LUAD-B02077 COSM334980 c.1206C>A p.P402P Substitution - coding silent 11:47238155-47238155 + TCGA-DK-A3WW-01 COSM3791523 c.1162G>A p.D388N Substitution - Missense 11:47237975-47237975 + CN-AML-CR-42-Dx COSM5424286 c.857C>T p.P286L Substitution - Missense 11:47234911-47234911 + TCGA-AP-A0LM-01 COSM927370 c.1116C>T p.I372I Substitution - coding silent 11:47237929-47237929 + TCGA-BC-A10R-01 COSM4935965 c.1266A>G p.E422E Substitution - coding silent 11:47238831-47238831 + HCC2998 COSM1981286 c.43A>C p.I15L Substitution - Missense 11:47215179-47215179 + S00936 COSM231246 c.868C>T p.P290S Substitution - Missense 11:47234922-47234922 + TCGA-G3-A25V-01 COSM4914708 c.851C>A p.S284* Substitution - Nonsense 11:47234905-47234905 + TCGA-AP-A059-01 COSM927367 c.803A>C p.K268T Substitution - Missense 11:47234857-47234857 + TCGA-Q1-A73O-01 COSM4835272 c.831G>T p.G277G Substitution - coding silent 11:47234885-47234885 + LC_S25 COSM1188223 c.733G>T p.V245L Substitution - Missense 11:47234787-47234787 + LOVO COSM1981306 c.1067A>G p.Y356C Substitution - Missense 11:47237880-47237880 + CN-AML-34-T COSM5424286 c.857C>T p.P286L Substitution - Missense 11:47234911-47234911 + I2L-P19Ta-Tumor-Biopsy COSM5360648 c.587G>A p.S196N Substitution - Missense 11:47232944-47232944 + TCGA-B6-A0IO-01 COSM429051 c.1187C>T p.S396L Substitution - Missense 11:47238000-47238000 + Pat_06_A COSM5838639 c.695G>A p.G232D Substitution - Missense 11:47234665-47234665 + B105-0-Tumor COSM1746268 c.716G>A p.R239K Substitution - Missense 11:47234770-47234770 + TCGA-G2-A2ES-01 COSM1298086 c.158T>C p.L53P Substitution - Missense 11:47216366-47216366 + TCGA-18-3407-01 COSM687994 c.575G>T p.R192L Substitution - Missense 11:47232932-47232932 + C0051T COSM4165798 c.1208T>C p.M403T Substitution - Missense 11:47238157-47238157 + TCGA-B5-A11N-01 COSM927366 c.575G>A p.R192Q Substitution - Missense 11:47232932-47232932 + TCGA-EI-6917-01 COSM3415887 c.1200C>A p.F400L Substitution - Missense 11:47238149-47238149 + CN-AML-19-T COSM5424286 c.857C>T p.P286L Substitution - Missense 11:47234911-47234911 + WA48 COSM239534 c.1281G>T p.K427N Substitution - Missense 11:47238846-47238846 + Pat_16_A COSM5838640 c.746C>T p.A249V Substitution - Missense 11:47234800-47234800 + CSCC-20-T COSM4461427 c.1205C>T p.P402L Substitution - Missense 11:47238154-47238154 + TCGA-13-0904-01 COSM70414 c.1012A>C p.T338P Substitution - Missense 11:47235401-47235401 + TCGA-GM-A2D9-01 COSM1746268 c.716G>A p.R239K Substitution - Missense 11:47234770-47234770 + CRC-02T COSM5453906 c.1023G>T p.K341N Substitution - Missense 11:47235412-47235412 + TCGA-D3-A1QA-06 COSM3447754 c.1076C>T p.P359L Substitution - Missense 11:47237889-47237889 + NB-1110 COSM1284432 c.936C>A p.I312I Substitution - coding silent 11:47235325-47235325 + PT09_1 COSM5895260 c.53_54insC p.R20fs*26 Insertion - Frameshift 11:47215189-47215190 + TCGA-D1-A16Y-01 COSM927368 c.965G>T p.C322F Substitution - Missense 11:47235354-47235354 + TCGA-AX-A06H-01 COSM927372 c.1277G>T p.R426L Substitution - Missense 11:47238842-47238842 + PT09_2 COSM5895260 c.53_54insC p.R20fs*26 Insertion - Frameshift 11:47215189-47215190 + TCGA-FW-A3R5-06 COSM3869220 c.869C>T p.P290L Substitution - Missense 11:47234923-47234923 + PT23_2 COSM5903778 c.227A>C p.H76P Substitution - Missense 11:47216435-47216435 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.700323;Hs.700335;Hs.700338 11p12-p11 600811

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.T338P c.1012A>C 11 47256952 OV A T Synonymous p.G179G c.537A>T 11 47254445 COREAD C A Missense p.P330H c.989C>A 11 47256929 CM C A Synonymous p.I312I c.936C>A 11 47256876 NB C G Missense p.I417M c.1251C>G 11 47260367 CM C G Missense p.L98V c.292C>G 11 47238436 LUSC C G Synonymous p.P27P c.81C>G 11 47236768 CM C T Missense p.A195V c.584C>T 11 47254492 GBM C T Missense p.H333Y c.997C>T 11 47256937 STAD C T Missense p.L167F c.499C>T 11 47254407 BLCA C T Missense p.P290S c.868C>T 11 47256473 CM C T Missense p.P290S c.868C>T 11 47256473 SCLC C T Missense p.P359L c.1076C>T 11 47259440 CM C T Missense p.R273C c.817C>T 11 47256422 HNSC C T Missense p.S396L c.1187C>T 11 47259551 BRCA C T Synonymous p.L167L c.501C>T 11 47254409 BLCA C T Synonymous p.V70V c.210C>T 11 47237969 ESCA G A Missense p.A128T c.382G>A 11 47238526 STAD G A Missense p.E234K c.700G>A 11 47256221 CM G A Missense p.R302Q c.905G>A 11 47256845 HNSC G A SpliceAcceptorSNV . c.1024-1G>A 11 47259387 LUSC G C Missense p.E33Q c.97G>C 11 47236784 BLCA G C Synonymous p.L207L c.621G>C 11 47256142 CM G T Missense p.C322F c.965G>T 11 47256905 UCEC G T Missense p.R192L c.575G>T 11 47254483 LUSC T C Missense p.L53P c.158T>C 11 47237917 BLCA T C Missense p.S379P c.1135T>C 11 47259499 UCEC