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 4621770 4621770 + Silent SNP C C G TCGA-CF-A3MI-01A-11D-A20D-08 TCGA-CF-A3MI-10A-01D-A20D-08 g.chr11:4621770C>G c.1194G>C c.(1192-1194)ctG>ctC p.L398L BLCA 11 4623475 4623475 + Silent SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:4623475G>A c.690C>T c.(688-690)aaC>aaT p.N230N BLCA 11 4623543 4623543 + Missense_Mutation SNP C C T TCGA-FD-A3SJ-01A-12D-A22Z-08 TCGA-FD-A3SJ-10A-01D-A22Z-08 g.chr11:4623543C>T c.622G>A c.(622-624)Gag>Aag p.E208K BLCA 11 4624510 4624510 + Missense_Mutation SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr11:4624510C>T c.487G>A c.(487-489)Gaa>Aaa p.E163K BLCA 11 4626603 4626603 + Nonsense_Mutation SNP C C T TCGA-C4-A0EZ-01A-21D-A10S-08 TCGA-C4-A0EZ-10A-01D-A10S-08 g.chr11:4626603C>T c.132G>A c.(130-132)tgG>tgA p.W44* BRCA 11 4621685 4621685 + Missense_Mutation SNP C C T TCGA-A8-A09R-01A-11W-A019-09 TCGA-A8-A09R-10A-01W-A021-09 g.chr11:4621685C>T c.1279G>A c.(1279-1281)Gtg>Atg p.V427M BRCA 11 4626420 4626420 + Silent SNP C C T TCGA-A2-A0EQ-01A-11W-A050-09 TCGA-A2-A0EQ-10A-01W-A055-09 g.chr11:4626420C>T c.315G>A c.(313-315)ctG>ctA p.L105L CESC 11 4623468 4623468 + Missense_Mutation SNP C C T TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr11:4623468C>T c.697G>A c.(697-699)Gag>Aag p.E233K COAD 11 4621713 4621713 + Silent SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr11:4621713C>T c.1251G>A c.(1249-1251)ccG>ccA p.P417P COAD 11 4621796 4621796 + Frame_Shift_Del DEL G G - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr11:4621796delG c.1168delC c.(1168-1170)cacfs p.H390fs COAD 11 4621818 4621818 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr11:4621818C>A c.1146G>T c.(1144-1146)aaG>aaT p.K382N COAD 11 4621926 4621926 + Silent SNP G G A TCGA-AA-3666-01A-02W-0900-09 TCGA-AA-3666-10A-01W-0900-09 g.chr11:4621926G>A c.1038C>T c.(1036-1038)atC>atT p.I346I COAD 11 4621937 4621937 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:4621937G>A c.1027C>T c.(1027-1029)Cgc>Tgc p.R343C COAD 11 4622019 4622019 + Silent SNP A A G TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chr11:4622019A>G c.945T>C c.(943-945)cgT>cgC p.R315R COAD 11 4622019 4622019 + Silent SNP A A G TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr11:4622019A>G c.945T>C c.(943-945)cgT>cgC p.R315R COAD 11 4622021 4622021 + Missense_Mutation SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr11:4622021G>A c.943C>T c.(943-945)Cgt>Tgt p.R315C COAD 11 4622021 4622021 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr11:4622021G>A c.943C>T c.(943-945)Cgt>Tgt p.R315C COAD 11 4622021 4622021 + Missense_Mutation SNP G G A TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr11:4622021G>A c.943C>T c.(943-945)Cgt>Tgt p.R315C COAD 11 4622349 4622349 + Missense_Mutation SNP G G A TCGA-A6-3807-01A-01W-0995-10 TCGA-A6-3807-11A-01W-0995-10 g.chr11:4622349G>A c.815C>T c.(814-816)tCt>tTt p.S272F COAD 11 4623541 4623541 + Missense_Mutation SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr11:4623541C>A c.624G>T c.(622-624)gaG>gaT p.E208D COAD 11 4626436 4626436 + Missense_Mutation SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:4626436C>T c.299G>A c.(298-300)cGc>cAc p.R100H COAD 11 4626437 4626437 + Missense_Mutation SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:4626437G>A c.298C>T c.(298-300)Cgc>Tgc p.R100C COADREAD 11 4621713 4621713 + Silent SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr11:4621713C>T c.1251G>A c.(1249-1251)ccG>ccA p.P417P COADREAD 11 4621796 4621796 + Frame_Shift_Del DEL G G - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr11:4621796delG c.1168delC c.(1168-1170)cacfs p.H390fs COADREAD 11 4621818 4621818 + Missense_Mutation SNP C C A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr11:4621818C>A c.1146G>T c.(1144-1146)aaG>aaT p.K382N COADREAD 11 4621926 4621926 + Silent SNP G G A TCGA-AA-3666-01A-02W-0900-09 TCGA-AA-3666-10A-01W-0900-09 g.chr11:4621926G>A c.1038C>T c.(1036-1038)atC>atT p.I346I COADREAD 11 4621937 4621937 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:4621937G>A c.1027C>T c.(1027-1029)Cgc>Tgc p.R343C COADREAD 11 4622019 4622019 + Silent SNP A A G TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chr11:4622019A>G c.945T>C c.(943-945)cgT>cgC p.R315R COADREAD 11 4622019 4622019 + Silent SNP A A G TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr11:4622019A>G c.945T>C c.(943-945)cgT>cgC p.R315R COADREAD 11 4622019 4622019 + Silent SNP A A G TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr11:4622019A>G c.945T>C c.(943-945)cgT>cgC p.R315R COADREAD 11 4622021 4622021 + Missense_Mutation SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr11:4622021G>A c.943C>T c.(943-945)Cgt>Tgt p.R315C COADREAD 11 4622021 4622021 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr11:4622021G>A c.943C>T c.(943-945)Cgt>Tgt p.R315C COADREAD 11 4622021 4622021 + Missense_Mutation SNP G G A TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr11:4622021G>A c.943C>T c.(943-945)Cgt>Tgt p.R315C COADREAD 11 4622349 4622349 + Missense_Mutation SNP G G A TCGA-A6-3807-01A-01W-0995-10 TCGA-A6-3807-11A-01W-0995-10 g.chr11:4622349G>A c.815C>T c.(814-816)tCt>tTt p.S272F COADREAD 11 4623541 4623541 + Missense_Mutation SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr11:4623541C>A c.624G>T c.(622-624)gaG>gaT p.E208D COADREAD 11 4626436 4626436 + Missense_Mutation SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr11:4626436C>T c.299G>A c.(298-300)cGc>cAc p.R100H COADREAD 11 4626437 4626437 + Missense_Mutation SNP G G A TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr11:4626437G>A c.298C>T c.(298-300)Cgc>Tgc p.R100C ESCA 11 4621685 4621685 + Missense_Mutation SNP C C T TCGA-L5-A8NW-01A-11D-A37C-09 TCGA-L5-A8NW-11A-11D-A37F-09 g.chr11:4621685C>T c.1279G>A c.(1279-1281)Gtg>Atg p.V427M ESCA 11 4622317 4622317 + Missense_Mutation SNP G G C TCGA-LN-A49X-01A-31D-A27G-09 TCGA-LN-A49X-10A-01D-A27G-09 g.chr11:4622317G>C c.847C>G c.(847-849)Ctg>Gtg p.L283V GBMLGG 11 4626616 4626616 + Missense_Mutation SNP A A G TCGA-DB-5277-01A-01D-1468-08 TCGA-DB-5277-10A-01D-1468-08 g.chr11:4626616A>G c.119T>C c.(118-120)cTc>cCc p.L40P HNSC 11 4621792 4621792 + Missense_Mutation SNP T T C TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chr11:4621792T>C c.1172A>G c.(1171-1173)tAt>tGt p.Y391C HNSC 11 4621844 4621844 + Missense_Mutation SNP C C G TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr11:4621844C>G c.1120G>C c.(1120-1122)Gta>Cta p.V374L HNSC 11 4621896 4621896 + Silent SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr11:4621896G>A c.1068C>T c.(1066-1068)ggC>ggT p.G356G HNSC 11 4622349 4622349 + Missense_Mutation SNP G G C TCGA-CR-7386-01A-11D-2012-08 TCGA-CR-7386-10A-01D-2013-08 g.chr11:4622349G>C c.815C>G c.(814-816)tCt>tGt p.S272C HNSC 11 4624492 4624492 + Nonsense_Mutation SNP G G A TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr11:4624492G>A c.505C>T c.(505-507)Cga>Tga p.R169* HNSC 11 4626315 4626315 + Missense_Mutation SNP C C G TCGA-CN-6023-01A-11D-1683-08 TCGA-CN-6023-10A-01D-1683-08 g.chr11:4626315C>G c.420G>C c.(418-420)gaG>gaC p.E140D HNSC 11 4626317 4626317 + Missense_Mutation SNP C C G TCGA-HD-8314-01A-11D-2394-08 TCGA-HD-8314-10A-01D-2394-08 g.chr11:4626317C>G c.418G>C c.(418-420)Gag>Cag p.E140Q KICH 11 4624492 4624492 + Nonsense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr11:4624492G>A c.505C>T c.(505-507)Cga>Tga p.R169* KIPAN 11 4621750 4621750 + Missense_Mutation SNP C C T TCGA-P4-A5EA-01A-11D-A28G-10 TCGA-P4-A5EA-11A-11D-A28G-10 g.chr11:4621750C>T c.1214G>A c.(1213-1215)cGa>cAa p.R405Q KIPAN 11 4624492 4624492 + Nonsense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr11:4624492G>A c.505C>T c.(505-507)Cga>Tga p.R169* KIRP 11 4621750 4621750 + Missense_Mutation SNP C C T TCGA-P4-A5EA-01A-11D-A28G-10 TCGA-P4-A5EA-11A-11D-A28G-10 g.chr11:4621750C>T c.1214G>A c.(1213-1215)cGa>cAa p.R405Q LGG 11 4626616 4626616 + Missense_Mutation SNP A A G TCGA-DB-5277-01A-01D-1468-08 TCGA-DB-5277-10A-01D-1468-08 g.chr11:4626616A>G c.119T>C c.(118-120)cTc>cCc p.L40P LIHC 11 4621894 4621894 + Missense_Mutation SNP C C T TCGA-DD-A3A8-01A-11D-A22F-10 TCGA-DD-A3A8-11A-11D-A22F-10 g.chr11:4621894C>T c.1070G>A c.(1069-1071)cGg>cAg p.R357Q LUAD 11 4621637 4621637 + Missense_Mutation SNP C C A TCGA-83-5908-01A-21D-2284-08 TCGA-83-5908-10A-01D-2284-08 g.chr11:4621637C>A c.1327G>T c.(1327-1329)Ggc>Tgc p.G443C LUAD 11 4621699 4621699 + Missense_Mutation SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr11:4621699C>A c.1265G>T c.(1264-1266)cGg>cTg p.R422L LUAD 11 4621864 4621864 + Missense_Mutation SNP C C T TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr11:4621864C>T c.1100G>A c.(1099-1101)aGg>aAg p.R367K LUAD 11 4621894 4621894 + Missense_Mutation SNP C C T TCGA-55-6982-01A-11D-1945-08 TCGA-55-6982-11A-01D-1945-08 g.chr11:4621894C>T c.1070G>A c.(1069-1071)cGg>cAg p.R357Q LUAD 11 4623587 4623587 + Missense_Mutation SNP C C T TCGA-78-7163-01A-12D-2063-08 TCGA-78-7163-11A-01D-2063-08 g.chr11:4623587C>T c.578G>A c.(577-579)cGa>cAa p.R193Q LUAD 11 4626536 4626536 + Missense_Mutation SNP T T A TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr11:4626536T>A c.199A>T c.(199-201)Agg>Tgg p.R67W LUSC 11 4621770 4621770 + Silent SNP C C T TCGA-66-2791-01A-01D-0983-08 TCGA-66-2791-11A-01D-0983-08 g.chr11:4621770C>T c.1194G>A c.(1192-1194)ctG>ctA p.L398L LUSC 11 4624558 4624558 + Missense_Mutation SNP C C T TCGA-18-3412-01A-01D-0983-08 TCGA-18-3412-11A-01D-0983-08 g.chr11:4624558C>T c.439G>A c.(439-441)Gag>Aag p.E147K LUSC 11 4626667 4626667 + Missense_Mutation SNP A A T TCGA-37-4133-01A-01D-1352-08 TCGA-37-4133-10A-01D-1352-08 g.chr11:4626667A>T c.68T>A c.(67-69)cTg>cAg p.L23Q OV 11 4622020 4622020 + Missense_Mutation SNP C C T TCGA-24-1545-01A-01W-0615-10 TCGA-24-1545-10A-01W-0615-10 g.chr11:4622020C>T c.944G>A c.(943-945)cGt>cAt p.R315H PAAD 11 4623634 4623634 + Silent SNP C C A TCGA-F2-A7TX-01A-33D-A38G-08 TCGA-F2-A7TX-10B-01D-A38J-08 g.chr11:4623634C>A c.531G>T c.(529-531)gtG>gtT p.V177V PAAD 11 4626372 4626372 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:4626372G>A c.363C>T c.(361-363)agC>agT p.S121S PAAD 11 4626710 4626710 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:4626710C>A c.25G>T c.(25-27)Gcc>Tcc p.A9S PRAD 11 4622021 4622021 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:4622021G>A c.943C>T c.(943-945)Cgt>Tgt p.R315C PRAD 11 4626487 4626487 + Missense_Mutation SNP C C T TCGA-EJ-7328-01A-31D-2114-08 TCGA-EJ-7328-10A-01D-2114-08 g.chr11:4626487C>T c.248G>A c.(247-249)cGt>cAt p.R83H READ 11 4622019 4622019 + Silent SNP A A G TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr11:4622019A>G c.945T>C c.(943-945)cgT>cgC p.R315R SKCM 11 4621530 4621530 + Silent SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr11:4621530G>A c.1434C>T c.(1432-1434)atC>atT p.I478I SKCM 11 4621703 4621703 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr11:4621703G>A c.1261C>T c.(1261-1263)Cgc>Tgc p.R421C SKCM 11 4621725 4621725 + Silent SNP G G A TCGA-EE-A20H-06A-11D-A197-08 TCGA-EE-A20H-10A-01D-A199-08 g.chr11:4621725G>A c.1239C>T c.(1237-1239)atC>atT p.I413I SKCM 11 4621926 4621926 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:4621926G>A c.1038C>T c.(1036-1038)atC>atT p.I346I SKCM 11 4622013 4622013 + Silent SNP G G A TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr11:4622013G>A c.951C>T c.(949-951)atC>atT p.I317I SKCM 11 4624525 4624525 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr11:4624525C>T c.472G>A c.(472-474)Gag>Aag p.E158K SKCM 11 4626489 4626489 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:4626489G>A c.246C>T c.(244-246)gtC>gtT p.V82V SKCM 11 4626492 4626492 + Frame_Shift_Del DEL T T - TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr11:4626492delT c.243delA c.(241-243)aaafs p.K81fs

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 4615695 4615695 single base substitution C G downstream_gene_variant BLCA-US 11 4616239 4616239 single base substitution C G downstream_gene_variant BLCA-US 11 4621770 4621770 single base substitution C G 3_prime_UTR_variant BLCA-US 11 4621770 4621770 single base substitution C G downstream_gene_variant BLCA-US 11 4621770 4621770 single base substitution C G synonymous_variant L398L 1194G>C BLCA-US 11 4623543 4623543 single base substitution C T 3_prime_UTR_variant BLCA-US 11 4623543 4623543 single base substitution C T 5_prime_UTR_variant BLCA-US 11 4623543 4623543 single base substitution C T exon_variant BLCA-US 11 4623543 4623543 single base substitution C T missense_variant E176K 526G>A BLCA-US 11 4623543 4623543 single base substitution C T missense_variant E208K 622G>A BLCA-US 11 4623543 4623543 single base substitution C T upstream_gene_variant BRCA-EU 11 4615369 4615369 single base substitution C T downstream_gene_variant BRCA-EU 11 4616547 4616547 single base substitution C G downstream_gene_variant BRCA-EU 11 4616641 4616641 single base substitution C G downstream_gene_variant BRCA-EU 11 4616648 4616648 single base substitution T C downstream_gene_variant BRCA-EU 11 4617689 4617689 single base substitution C T downstream_gene_variant BRCA-EU 11 4617899 4617899 single base substitution T A downstream_gene_variant BRCA-EU 11 4618104 4618104 single base substitution T C downstream_gene_variant BRCA-EU 11 4618854 4618854 single base substitution A G downstream_gene_variant BRCA-EU 11 4619269 4619270 deletion of <=200bp AC - downstream_gene_variant BRCA-EU 11 4619469 4619469 single base substitution C A downstream_gene_variant BRCA-EU 11 4620902 4620902 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 4620902 4620902 single base substitution G C downstream_gene_variant BRCA-EU 11 4621835 4621835 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 4621835 4621835 single base substitution G C downstream_gene_variant BRCA-EU 11 4621835 4621835 single base substitution G C missense_variant Q377E 1129C>G BRCA-EU 11 4621994 4621994 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 4621994 4621994 single base substitution G A downstream_gene_variant BRCA-EU 11 4621994 4621994 single base substitution G A missense_variant R101C 301C>T BRCA-EU 11 4621994 4621994 single base substitution G A missense_variant R324C 970C>T BRCA-EU 11 4623058 4623058 single base substitution C T downstream_gene_variant BRCA-EU 11 4623058 4623058 single base substitution C T exon_variant BRCA-EU 11 4623058 4623058 single base substitution C T intron_variant BRCA-EU 11 4623058 4623058 single base substitution C T upstream_gene_variant BRCA-EU 11 4626165 4626165 single base substitution C T intron_variant BRCA-EU 11 4626165 4626165 single base substitution C T upstream_gene_variant BRCA-EU 11 4627823 4627823 single base substitution G C intron_variant BRCA-EU 11 4628559 4628559 single base substitution G A intron_variant BRCA-EU 11 4629326 4629326 single base substitution C G 5_prime_UTR_variant BRCA-EU 11 4629326 4629326 single base substitution C G exon_variant BRCA-EU 11 4629564 4629564 single base substitution G C upstream_gene_variant BRCA-EU 11 4629607 4629607 single base substitution G C upstream_gene_variant BRCA-EU 11 4629730 4629730 single base substitution T C upstream_gene_variant BRCA-EU 11 4629753 4629753 single base substitution C T upstream_gene_variant BRCA-EU 11 4630226 4630226 single base substitution G A upstream_gene_variant BRCA-EU 11 4630791 4630791 single base substitution C G upstream_gene_variant BRCA-EU 11 4631252 4631252 single base substitution C T upstream_gene_variant BRCA-EU 11 4631603 4631603 single base substitution T C upstream_gene_variant BRCA-EU 11 4631626 4631626 single base substitution C T upstream_gene_variant BRCA-EU 11 4632562 4632562 single base substitution C G upstream_gene_variant BRCA-EU 11 4632709 4632709 single base substitution C A upstream_gene_variant BRCA-EU 11 4633133 4633133 single base substitution A G upstream_gene_variant BRCA-FR 11 4616153 4616153 single base substitution C T downstream_gene_variant BRCA-FR 11 4623058 4623058 single base substitution C T downstream_gene_variant BRCA-FR 11 4623058 4623058 single base substitution C T exon_variant BRCA-FR 11 4623058 4623058 single base substitution C T intron_variant BRCA-FR 11 4623058 4623058 single base substitution C T upstream_gene_variant BRCA-FR 11 4627511 4627511 single base substitution G A intron_variant BRCA-FR 11 4627511 4627511 single base substitution G A upstream_gene_variant BRCA-FR 11 4631468 4631468 single base substitution G C upstream_gene_variant BRCA-US 11 4615427 4615427 single base substitution C A downstream_gene_variant BRCA-US 11 4621685 4621685 single base substitution C T 3_prime_UTR_variant BRCA-US 11 4621685 4621685 single base substitution C T downstream_gene_variant BRCA-US 11 4621685 4621685 single base substitution C T missense_variant V427M 1279G>A BRCA-US 11 4626420 4626420 single base substitution C T exon_variant BRCA-US 11 4626420 4626420 single base substitution C T intron_variant BRCA-US 11 4626420 4626420 single base substitution C T synonymous_variant L105L 315G>A BRCA-US 11 4626420 4626420 single base substitution C T upstream_gene_variant BTCA-JP 11 4626874 4626874 deletion of <=200bp G - intron_variant BTCA-JP 11 4626874 4626874 deletion of <=200bp G - upstream_gene_variant CESC-US 11 4615380 4615380 single base substitution A C downstream_gene_variant CESC-US 11 4623468 4623468 single base substitution C T 3_prime_UTR_variant CESC-US 11 4623468 4623468 single base substitution C T downstream_gene_variant CESC-US 11 4623468 4623468 single base substitution C T exon_variant CESC-US 11 4623468 4623468 single base substitution C T missense_variant E10K 28G>A CESC-US 11 4623468 4623468 single base substitution C T missense_variant E233K 697G>A CESC-US 11 4623468 4623468 single base substitution C T upstream_gene_variant CLLE-ES 11 4618256 4618256 single base substitution T C downstream_gene_variant COAD-US 11 4615525 4615525 single base substitution T C downstream_gene_variant COAD-US 11 4615644 4615644 single base substitution C T downstream_gene_variant COAD-US 11 4615722 4615722 single base substitution G A downstream_gene_variant COAD-US 11 4621796 4621796 deletion of <=200bp G - 3_prime_UTR_variant COAD-US 11 4621796 4621796 deletion of <=200bp G - downstream_gene_variant COAD-US 11 4621796 4621796 deletion of <=200bp G - frameshift_variant H390 COAD-US 11 4621937 4621937 single base substitution G A 3_prime_UTR_variant COAD-US 11 4621937 4621937 single base substitution G A downstream_gene_variant COAD-US 11 4621937 4621937 single base substitution G A missense_variant R120C 358C>T COAD-US 11 4621937 4621937 single base substitution G A missense_variant R343C 1027C>T COAD-US 11 4626436 4626436 single base substitution C T exon_variant COAD-US 11 4626436 4626436 single base substitution C T intron_variant COAD-US 11 4626436 4626436 single base substitution C T missense_variant R100H 299G>A COAD-US 11 4626436 4626436 single base substitution C T upstream_gene_variant COCA-CN 11 4615224 4615224 single base substitution C A downstream_gene_variant COCA-CN 11 4621666 4621666 single base substitution T C 3_prime_UTR_variant COCA-CN 11 4621666 4621666 single base substitution T C downstream_gene_variant COCA-CN 11 4621666 4621666 single base substitution T C missense_variant D433G 1298A>G COCA-CN 11 4623106 4623106 single base substitution T C downstream_gene_variant COCA-CN 11 4623106 4623106 single base substitution T C exon_variant COCA-CN 11 4623106 4623106 single base substitution T C intron_variant COCA-CN 11 4623106 4623106 single base substitution T C upstream_gene_variant COCA-CN 11 4626436 4626436 single base substitution C T exon_variant COCA-CN 11 4626436 4626436 single base substitution C T intron_variant COCA-CN 11 4626436 4626436 single base substitution C T missense_variant R100H 299G>A COCA-CN 11 4626436 4626436 single base substitution C T upstream_gene_variant ESAD-UK 11 4618102 4618102 single base substitution A T downstream_gene_variant ESAD-UK 11 4619023 4619023 single base substitution G C downstream_gene_variant ESAD-UK 11 4619029 4619029 single base substitution G A downstream_gene_variant ESAD-UK 11 4620502 4620502 single base substitution G A 3_prime_UTR_variant ESAD-UK 11 4620502 4620502 single base substitution G A downstream_gene_variant ESAD-UK 11 4620949 4620949 single base substitution C A 3_prime_UTR_variant ESAD-UK 11 4620949 4620949 single base substitution C A downstream_gene_variant ESAD-UK 11 4621872 4621872 single base substitution C T 3_prime_UTR_variant ESAD-UK 11 4621872 4621872 single base substitution C T downstream_gene_variant ESAD-UK 11 4621872 4621872 single base substitution C T synonymous_variant V141V 423G>A ESAD-UK 11 4621872 4621872 single base substitution C T synonymous_variant V364V 1092G>A ESAD-UK 11 4623414 4623414 single base substitution T C 3_prime_UTR_variant ESAD-UK 11 4623414 4623414 single base substitution T C downstream_gene_variant ESAD-UK 11 4623414 4623414 single base substitution T C exon_variant ESAD-UK 11 4623414 4623414 single base substitution T C missense_variant R251G 751A>G ESAD-UK 11 4623414 4623414 single base substitution T C missense_variant R28G 82A>G ESAD-UK 11 4623414 4623414 single base substitution T C upstream_gene_variant ESAD-UK 11 4624874 4624874 single base substitution T C intron_variant ESAD-UK 11 4624874 4624874 single base substitution T C upstream_gene_variant ESAD-UK 11 4624976 4624976 single base substitution C A intron_variant ESAD-UK 11 4624976 4624976 single base substitution C A upstream_gene_variant ESAD-UK 11 4625011 4625011 single base substitution C T intron_variant ESAD-UK 11 4625011 4625011 single base substitution C T upstream_gene_variant ESAD-UK 11 4627040 4627040 single base substitution C T intron_variant ESAD-UK 11 4627040 4627040 single base substitution C T upstream_gene_variant ESAD-UK 11 4627128 4627128 single base substitution A C intron_variant ESAD-UK 11 4627128 4627128 single base substitution A C upstream_gene_variant ESAD-UK 11 4627624 4627624 single base substitution T C intron_variant ESAD-UK 11 4627624 4627624 single base substitution T C upstream_gene_variant ESAD-UK 11 4627895 4627895 single base substitution T C intron_variant ESAD-UK 11 4629604 4629604 single base substitution T G upstream_gene_variant ESAD-UK 11 4632660 4632660 single base substitution C T upstream_gene_variant ESAD-UK 11 4632803 4632803 single base substitution A T upstream_gene_variant ESAD-UK 11 4633398 4633398 single base substitution C T upstream_gene_variant ESAD-UK 11 4634208 4634208 single base substitution G A upstream_gene_variant ESAD-UK 11 4634361 4634361 single base substitution T G upstream_gene_variant ESCA-CN 11 4621859 4621859 single base substitution C G 3_prime_UTR_variant ESCA-CN 11 4621859 4621859 single base substitution C G downstream_gene_variant ESCA-CN 11 4621859 4621859 single base substitution C G missense_variant E369Q 1105G>C ESCA-CN 11 4623406 4623406 single base substitution C T 3_prime_UTR_variant ESCA-CN 11 4623406 4623406 single base substitution C T downstream_gene_variant ESCA-CN 11 4623406 4623406 single base substitution C T exon_variant ESCA-CN 11 4623406 4623406 single base substitution C T synonymous_variant Q253Q 759G>A ESCA-CN 11 4623406 4623406 single base substitution C T synonymous_variant Q30Q 90G>A ESCA-CN 11 4623406 4623406 single base substitution C T upstream_gene_variant GBM-US 11 4615416 4615416 single base substitution G A downstream_gene_variant GBM-US 11 4616048 4616048 deletion of <=200bp G - downstream_gene_variant KIRC-US 11 4616186 4616186 single base substitution G C downstream_gene_variant KIRP-US 11 4621750 4621750 single base substitution C T 3_prime_UTR_variant KIRP-US 11 4621750 4621750 single base substitution C T downstream_gene_variant KIRP-US 11 4621750 4621750 single base substitution C T missense_variant R405Q 1214G>A KIRP-US 11 4621934 4621934 single base substitution A G 3_prime_UTR_variant KIRP-US 11 4621934 4621934 single base substitution A G downstream_gene_variant KIRP-US 11 4621934 4621934 single base substitution A G missense_variant Y121H 361T>C KIRP-US 11 4621934 4621934 single base substitution A G missense_variant Y344H 1030T>C LAML-KR 11 4615869 4615869 single base substitution C G downstream_gene_variant LGG-US 11 4626616 4626616 single base substitution A G exon_variant LGG-US 11 4626616 4626616 single base substitution A G intron_variant LGG-US 11 4626616 4626616 single base substitution A G missense_variant L40P 119T>C LGG-US 11 4626616 4626616 single base substitution A G upstream_gene_variant LICA-CN 11 4615821 4615821 single base substitution C A downstream_gene_variant LICA-CN 11 4621770 4621770 single base substitution C A 3_prime_UTR_variant LICA-CN 11 4621770 4621770 single base substitution C A downstream_gene_variant LICA-CN 11 4621770 4621770 single base substitution C A synonymous_variant L398L 1194G>T LICA-FR 11 4624537 4624537 single base substitution T A 5_prime_UTR_variant LICA-FR 11 4624537 4624537 single base substitution T A exon_variant LICA-FR 11 4624537 4624537 single base substitution T A intron_variant LICA-FR 11 4624537 4624537 single base substitution T A stop_gained K154* 460A>T LICA-FR 11 4624537 4624537 single base substitution T A upstream_gene_variant LICA-FR 11 4626369 4626369 single base substitution C T exon_variant LICA-FR 11 4626369 4626369 single base substitution C T intron_variant LICA-FR 11 4626369 4626369 single base substitution C T synonymous_variant Q122Q 366G>A LICA-FR 11 4626369 4626369 single base substitution C T upstream_gene_variant LIHC-US 11 4621894 4621894 single base substitution C T 3_prime_UTR_variant LIHC-US 11 4621894 4621894 single base substitution C T downstream_gene_variant LIHC-US 11 4621894 4621894 single base substitution C T missense_variant R134Q 401G>A LIHC-US 11 4621894 4621894 single base substitution C T missense_variant R357Q 1070G>A LINC-JP 11 4616227 4616227 single base substitution C G downstream_gene_variant LINC-JP 11 4624768 4624768 single base substitution C A intron_variant LINC-JP 11 4624768 4624768 single base substitution C A upstream_gene_variant LINC-JP 11 4626351 4626351 single base substitution G C exon_variant LINC-JP 11 4626351 4626351 single base substitution G C intron_variant LINC-JP 11 4626351 4626351 single base substitution G C synonymous_variant A128A 384C>G LINC-JP 11 4626351 4626351 single base substitution G C upstream_gene_variant LINC-JP 11 4627763 4627763 single base substitution C A intron_variant LINC-JP 11 4627763 4627763 single base substitution C A upstream_gene_variant LINC-JP 11 4633910 4633910 single base substitution G T upstream_gene_variant LIRI-JP 11 4616080 4616080 single base substitution A G downstream_gene_variant LIRI-JP 11 4616131 4616131 single base substitution T C downstream_gene_variant LIRI-JP 11 4616753 4616753 single base substitution T A downstream_gene_variant LIRI-JP 11 4620404 4620404 single base substitution T A 3_prime_UTR_variant LIRI-JP 11 4620404 4620404 single base substitution T A downstream_gene_variant LIRI-JP 11 4620508 4620508 single base substitution T C 3_prime_UTR_variant LIRI-JP 11 4620508 4620508 single base substitution T C downstream_gene_variant LIRI-JP 11 4621773 4621773 single base substitution C T 3_prime_UTR_variant LIRI-JP 11 4621773 4621773 single base substitution C T downstream_gene_variant LIRI-JP 11 4621773 4621773 single base substitution C T synonymous_variant R397R 1191G>A LIRI-JP 11 4622367 4622367 single base substitution G C downstream_gene_variant LIRI-JP 11 4622367 4622367 single base substitution G C exon_variant LIRI-JP 11 4622367 4622367 single base substitution G C intron_variant LIRI-JP 11 4622805 4622805 single base substitution G A downstream_gene_variant LIRI-JP 11 4622805 4622805 single base substitution G A intron_variant LIRI-JP 11 4622805 4622805 single base substitution G A upstream_gene_variant LIRI-JP 11 4623106 4623106 single base substitution T C downstream_gene_variant LIRI-JP 11 4623106 4623106 single base substitution T C exon_variant LIRI-JP 11 4623106 4623106 single base substitution T C intron_variant LIRI-JP 11 4623106 4623106 single base substitution T C upstream_gene_variant LIRI-JP 11 4624511 4624511 insertion of <=200bp - A 5_prime_UTR_variant LIRI-JP 11 4624511 4624511 insertion of <=200bp - A exon_variant LIRI-JP 11 4624511 4624511 insertion of <=200bp - A frameshift_variant L162L? LIRI-JP 11 4624511 4624511 insertion of <=200bp - A intron_variant LIRI-JP 11 4624511 4624511 insertion of <=200bp - A upstream_gene_variant LIRI-JP 11 4628110 4628110 single base substitution T C intron_variant LIRI-JP 11 4629853 4629853 single base substitution T C upstream_gene_variant LIRI-JP 11 4630324 4630324 single base substitution T G upstream_gene_variant LIRI-JP 11 4632104 4632104 single base substitution T C upstream_gene_variant LUSC-KR 11 4615903 4615903 single base substitution G A downstream_gene_variant LUSC-KR 11 4624317 4624317 single base substitution C A intron_variant LUSC-KR 11 4624317 4624317 single base substitution C A upstream_gene_variant LUSC-KR 11 4629494 4629494 single base substitution G T upstream_gene_variant LUSC-KR 11 4631427 4631427 single base substitution G A upstream_gene_variant LUSC-KR 11 4634180 4634180 single base substitution C A upstream_gene_variant LUSC-US 11 4615690 4615690 single base substitution C G downstream_gene_variant LUSC-US 11 4615724 4615724 single base substitution C T downstream_gene_variant LUSC-US 11 4621770 4621770 single base substitution C T 3_prime_UTR_variant LUSC-US 11 4621770 4621770 single base substitution C T downstream_gene_variant LUSC-US 11 4621770 4621770 single base substitution C T synonymous_variant L398L 1194G>A LUSC-US 11 4624558 4624558 single base substitution C T 5_prime_UTR_variant LUSC-US 11 4624558 4624558 single base substitution C T exon_variant LUSC-US 11 4624558 4624558 single base substitution C T intron_variant LUSC-US 11 4624558 4624558 single base substitution C T missense_variant E147K 439G>A LUSC-US 11 4624558 4624558 single base substitution C T upstream_gene_variant LUSC-US 11 4626667 4626667 single base substitution A T exon_variant LUSC-US 11 4626667 4626667 single base substitution A T intron_variant LUSC-US 11 4626667 4626667 single base substitution A T missense_variant L23Q 68T>A LUSC-US 11 4626667 4626667 single base substitution A T upstream_gene_variant MALY-DE 11 4619269 4619270 deletion of <=200bp AC - downstream_gene_variant MALY-DE 11 4623398 4623398 single base substitution A G 3_prime_UTR_variant MALY-DE 11 4623398 4623398 single base substitution A G downstream_gene_variant MALY-DE 11 4623398 4623398 single base substitution A G exon_variant MALY-DE 11 4623398 4623398 single base substitution A G missense_variant V256A 767T>C MALY-DE 11 4623398 4623398 single base substitution A G missense_variant V33A 98T>C MALY-DE 11 4623398 4623398 single base substitution A G upstream_gene_variant MALY-DE 11 4627486 4627486 single base substitution A G intron_variant MALY-DE 11 4627486 4627486 single base substitution A G upstream_gene_variant MALY-DE 11 4634315 4634315 single base substitution C A upstream_gene_variant MELA-AU 11 4615106 4615106 single base substitution G A downstream_gene_variant MELA-AU 11 4615837 4615837 single base substitution G T downstream_gene_variant MELA-AU 11 4616015 4616015 single base substitution G A downstream_gene_variant MELA-AU 11 4616337 4616337 single base substitution G A downstream_gene_variant MELA-AU 11 4616477 4616477 single base substitution G A downstream_gene_variant MELA-AU 11 4616772 4616772 single base substitution G A downstream_gene_variant MELA-AU 11 4617299 4617299 single base substitution A G downstream_gene_variant MELA-AU 11 4617468 4617468 single base substitution G A downstream_gene_variant MELA-AU 11 4617550 4617550 single base substitution G C downstream_gene_variant MELA-AU 11 4617711 4617711 single base substitution G A downstream_gene_variant MELA-AU 11 4618357 4618357 single base substitution G A downstream_gene_variant MELA-AU 11 4618664 4618664 single base substitution G A downstream_gene_variant MELA-AU 11 4618669 4618669 single base substitution G A downstream_gene_variant MELA-AU 11 4618830 4618830 single base substitution C T downstream_gene_variant MELA-AU 11 4619595 4619595 single base substitution G A downstream_gene_variant MELA-AU 11 4619867 4619867 single base substitution C T downstream_gene_variant MELA-AU 11 4620261 4620261 single base substitution C A 3_prime_UTR_variant MELA-AU 11 4620261 4620261 single base substitution C A downstream_gene_variant MELA-AU 11 4620444 4620445 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 11 4620444 4620445 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 4620751 4620751 single base substitution C T 3_prime_UTR_variant MELA-AU 11 4620751 4620751 single base substitution C T downstream_gene_variant MELA-AU 11 4620764 4620764 single base substitution C T 3_prime_UTR_variant MELA-AU 11 4620764 4620764 single base substitution C T downstream_gene_variant MELA-AU 11 4620999 4620999 single base substitution G T 3_prime_UTR_variant MELA-AU 11 4620999 4620999 single base substitution G T downstream_gene_variant MELA-AU 11 4621098 4621098 single base substitution G A 3_prime_UTR_variant MELA-AU 11 4621098 4621098 single base substitution G A downstream_gene_variant MELA-AU 11 4621173 4621173 single base substitution G A 3_prime_UTR_variant MELA-AU 11 4621173 4621173 single base substitution G A downstream_gene_variant MELA-AU 11 4621206 4621206 single base substitution G A 3_prime_UTR_variant MELA-AU 11 4621206 4621206 single base substitution G A downstream_gene_variant MELA-AU 11 4621289 4621289 single base substitution G A 3_prime_UTR_variant MELA-AU 11 4621289 4621289 single base substitution G A downstream_gene_variant MELA-AU 11 4621387 4621387 single base substitution G A 3_prime_UTR_variant MELA-AU 11 4621387 4621387 single base substitution G A downstream_gene_variant MELA-AU 11 4621626 4621626 single base substitution G A 3_prime_UTR_variant MELA-AU 11 4621626 4621626 single base substitution G A downstream_gene_variant MELA-AU 11 4621626 4621626 single base substitution G A synonymous_variant I446I 1338C>T MELA-AU 11 4621844 4621844 single base substitution C T 3_prime_UTR_variant MELA-AU 11 4621844 4621844 single base substitution C T downstream_gene_variant MELA-AU 11 4621844 4621844 single base substitution C T missense_variant V374I 1120G>A MELA-AU 11 4622066 4622066 single base substitution A T downstream_gene_variant MELA-AU 11 4622066 4622066 single base substitution A T intron_variant MELA-AU 11 4622503 4622503 single base substitution C T downstream_gene_variant MELA-AU 11 4622503 4622503 single base substitution C T exon_variant MELA-AU 11 4622503 4622503 single base substitution C T intron_variant MELA-AU 11 4622861 4622861 single base substitution G A downstream_gene_variant MELA-AU 11 4622861 4622861 single base substitution G A intron_variant MELA-AU 11 4622861 4622861 single base substitution G A upstream_gene_variant MELA-AU 11 4622968 4622968 single base substitution G A downstream_gene_variant MELA-AU 11 4622968 4622968 single base substitution G A exon_variant MELA-AU 11 4622968 4622968 single base substitution G A intron_variant MELA-AU 11 4622968 4622968 single base substitution G A upstream_gene_variant MELA-AU 11 4623140 4623140 single base substitution G A downstream_gene_variant MELA-AU 11 4623140 4623140 single base substitution G A exon_variant MELA-AU 11 4623140 4623140 single base substitution G A intron_variant MELA-AU 11 4623140 4623140 single base substitution G A upstream_gene_variant MELA-AU 11 4624001 4624001 single base substitution C G intron_variant MELA-AU 11 4624001 4624001 single base substitution C G upstream_gene_variant MELA-AU 11 4624327 4624327 single base substitution G A intron_variant MELA-AU 11 4624327 4624327 single base substitution G A upstream_gene_variant MELA-AU 11 4624448 4624448 single base substitution A C intron_variant MELA-AU 11 4624448 4624448 single base substitution A C upstream_gene_variant MELA-AU 11 4625329 4625329 single base substitution C A intron_variant MELA-AU 11 4625329 4625329 single base substitution C A upstream_gene_variant MELA-AU 11 4625554 4625554 single base substitution C T intron_variant MELA-AU 11 4625554 4625554 single base substitution C T upstream_gene_variant MELA-AU 11 4625555 4625555 single base substitution G A intron_variant MELA-AU 11 4625555 4625555 single base substitution G A upstream_gene_variant MELA-AU 11 4625743 4625743 single base substitution G A intron_variant MELA-AU 11 4625743 4625743 single base substitution G A upstream_gene_variant MELA-AU 11 4626071 4626071 single base substitution G A intron_variant MELA-AU 11 4626071 4626071 single base substitution G A upstream_gene_variant MELA-AU 11 4626076 4626076 single base substitution G A intron_variant MELA-AU 11 4626076 4626076 single base substitution G A upstream_gene_variant MELA-AU 11 4626119 4626119 single base substitution G A intron_variant MELA-AU 11 4626119 4626119 single base substitution G A upstream_gene_variant MELA-AU 11 4626123 4626123 single base substitution G A intron_variant MELA-AU 11 4626123 4626123 single base substitution G A upstream_gene_variant MELA-AU 11 4626150 4626150 single base substitution G A intron_variant MELA-AU 11 4626150 4626150 single base substitution G A upstream_gene_variant MELA-AU 11 4626492 4626492 deletion of <=200bp T - exon_variant MELA-AU 11 4626492 4626492 deletion of <=200bp T - frameshift_variant K81 MELA-AU 11 4626492 4626492 deletion of <=200bp T - intron_variant MELA-AU 11 4626492 4626492 deletion of <=200bp T - upstream_gene_variant MELA-AU 11 4626698 4626698 single base substitution C T exon_variant MELA-AU 11 4626698 4626698 single base substitution C T intron_variant MELA-AU 11 4626698 4626698 single base substitution C T missense_variant E13K 37G>A MELA-AU 11 4626698 4626698 single base substitution C T upstream_gene_variant MELA-AU 11 4626709 4626709 single base substitution G A exon_variant MELA-AU 11 4626709 4626709 single base substitution G A intron_variant MELA-AU 11 4626709 4626709 single base substitution G A missense_variant A9V 26C>T MELA-AU 11 4626709 4626709 single base substitution G A upstream_gene_variant MELA-AU 11 4626878 4626878 single base substitution G A intron_variant MELA-AU 11 4626878 4626878 single base substitution G A upstream_gene_variant MELA-AU 11 4627338 4627338 single base substitution C T intron_variant MELA-AU 11 4627338 4627338 single base substitution C T upstream_gene_variant MELA-AU 11 4627773 4627773 single base substitution G A intron_variant MELA-AU 11 4627773 4627773 single base substitution G A upstream_gene_variant MELA-AU 11 4627774 4627774 single base substitution A G intron_variant MELA-AU 11 4627774 4627774 single base substitution A G upstream_gene_variant MELA-AU 11 4628091 4628091 single base substitution G A intron_variant MELA-AU 11 4629001 4629001 single base substitution G T intron_variant MELA-AU 11 4629522 4629522 single base substitution C T upstream_gene_variant MELA-AU 11 4629829 4629830 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 4630840 4630840 single base substitution G A upstream_gene_variant MELA-AU 11 4630896 4630896 single base substitution G A upstream_gene_variant MELA-AU 11 4630981 4630981 single base substitution C T upstream_gene_variant MELA-AU 11 4631081 4631081 single base substitution C T upstream_gene_variant MELA-AU 11 4631369 4631369 single base substitution G A upstream_gene_variant MELA-AU 11 4631371 4631372 multiple base substitution (>=2bp and <=200bp) GA AG upstream_gene_variant MELA-AU 11 4631747 4631747 single base substitution C T upstream_gene_variant MELA-AU 11 4632074 4632074 single base substitution G A upstream_gene_variant MELA-AU 11 4632607 4632607 single base substitution C T upstream_gene_variant MELA-AU 11 4632654 4632654 single base substitution C T upstream_gene_variant MELA-AU 11 4633216 4633216 single base substitution C T upstream_gene_variant MELA-AU 11 4633259 4633259 single base substitution G A upstream_gene_variant MELA-AU 11 4633563 4633563 single base substitution G A upstream_gene_variant MELA-AU 11 4633578 4633578 single base substitution T A upstream_gene_variant OV-AU 11 4617565 4617565 single base substitution G A downstream_gene_variant OV-AU 11 4618550 4618550 single base substitution C T downstream_gene_variant OV-AU 11 4619725 4619725 single base substitution A C downstream_gene_variant OV-AU 11 4625016 4625016 single base substitution T C intron_variant OV-AU 11 4625016 4625016 single base substitution T C upstream_gene_variant OV-AU 11 4625045 4625045 single base substitution C T intron_variant OV-AU 11 4625045 4625045 single base substitution C T upstream_gene_variant OV-AU 11 4628356 4628356 single base substitution C A intron_variant OV-AU 11 4630119 4630119 single base substitution A T upstream_gene_variant OV-AU 11 4630559 4630559 single base substitution A G upstream_gene_variant PACA-AU 11 4620836 4620836 single base substitution A G 3_prime_UTR_variant PACA-AU 11 4620836 4620836 single base substitution A G downstream_gene_variant PACA-AU 11 4623433 4623433 single base substitution C T 3_prime_UTR_variant PACA-AU 11 4623433 4623433 single base substitution C T downstream_gene_variant PACA-AU 11 4623433 4623433 single base substitution C T exon_variant PACA-AU 11 4623433 4623433 single base substitution C T missense_variant M21I 63G>A PACA-AU 11 4623433 4623433 single base substitution C T missense_variant M244I 732G>A PACA-AU 11 4623433 4623433 single base substitution C T upstream_gene_variant PACA-AU 11 4624478 4624478 single base substitution C A 5_prime_UTR_variant PACA-AU 11 4624478 4624478 single base substitution C A exon_variant PACA-AU 11 4624478 4624478 single base substitution C A intron_variant PACA-AU 11 4624478 4624478 single base substitution C A missense_variant W173C 519G>T PACA-AU 11 4624478 4624478 single base substitution C A upstream_gene_variant PACA-AU 11 4625492 4625492 deletion of <=200bp A - intron_variant PACA-AU 11 4625492 4625492 deletion of <=200bp A - upstream_gene_variant PACA-AU 11 4626332 4626332 single base substitution C T exon_variant PACA-AU 11 4626332 4626332 single base substitution C T intron_variant PACA-AU 11 4626332 4626332 single base substitution C T missense_variant E135K 403G>A PACA-AU 11 4626332 4626332 single base substitution C T upstream_gene_variant PACA-AU 11 4634133 4634133 single base substitution G T upstream_gene_variant PACA-CA 11 4615791 4615791 single base substitution T C downstream_gene_variant PACA-CA 11 4621026 4621026 single base substitution G C 3_prime_UTR_variant PACA-CA 11 4621026 4621026 single base substitution G C downstream_gene_variant PACA-CA 11 4624864 4624868 deletion of <=200bp CTTAT - intron_variant PACA-CA 11 4624864 4624868 deletion of <=200bp CTTAT - upstream_gene_variant PACA-CA 11 4625370 4625370 single base substitution T A intron_variant PACA-CA 11 4625370 4625370 single base substitution T A upstream_gene_variant PAEN-AU 11 4628279 4628279 single base substitution A G intron_variant PBCA-DE 11 4616143 4616143 single base substitution T C downstream_gene_variant PBCA-DE 11 4619269 4619270 deletion of <=200bp AC - downstream_gene_variant PBCA-DE 11 4624864 4624864 single base substitution C A intron_variant PBCA-DE 11 4624864 4624864 single base substitution C A upstream_gene_variant PBCA-DE 11 4626422 4626422 single base substitution G A exon_variant PBCA-DE 11 4626422 4626422 single base substitution G A intron_variant PBCA-DE 11 4626422 4626422 single base substitution G A synonymous_variant L105L 313C>T PBCA-DE 11 4626422 4626422 single base substitution G A upstream_gene_variant PBCA-DE 11 4626621 4626621 single base substitution G T exon_variant PBCA-DE 11 4626621 4626621 single base substitution G T intron_variant PBCA-DE 11 4626621 4626621 single base substitution G T missense_variant S38R 114C>A PBCA-DE 11 4626621 4626621 single base substitution G T upstream_gene_variant PRAD-CA 11 4628281 4628281 single base substitution A C intron_variant PRAD-UK 11 4633656 4633656 single base substitution G A upstream_gene_variant PRAD-US 11 4626487 4626487 single base substitution C T exon_variant PRAD-US 11 4626487 4626487 single base substitution C T intron_variant PRAD-US 11 4626487 4626487 single base substitution C T missense_variant R83H 248G>A PRAD-US 11 4626487 4626487 single base substitution C T upstream_gene_variant READ-US 11 4615444 4615444 single base substitution G A downstream_gene_variant READ-US 11 4622302 4622302 single base substitution C G 3_prime_UTR_variant READ-US 11 4622302 4622302 single base substitution C G downstream_gene_variant READ-US 11 4622302 4622302 single base substitution C G exon_variant READ-US 11 4622302 4622302 single base substitution C G missense_variant D288H 862G>C READ-US 11 4622302 4622302 single base substitution C G missense_variant D65H 193G>C RECA-EU 11 4617302 4617302 single base substitution C G downstream_gene_variant RECA-EU 11 4624153 4624153 single base substitution A G intron_variant RECA-EU 11 4624153 4624153 single base substitution A G upstream_gene_variant RECA-EU 11 4625368 4625368 single base substitution T A intron_variant RECA-EU 11 4625368 4625368 single base substitution T A upstream_gene_variant SKCA-BR 11 4617873 4617873 single base substitution A G downstream_gene_variant SKCA-BR 11 4619728 4619728 single base substitution G A downstream_gene_variant SKCA-BR 11 4623761 4623761 single base substitution G A intron_variant SKCA-BR 11 4623761 4623761 single base substitution G A upstream_gene_variant SKCA-BR 11 4623793 4623793 single base substitution T C intron_variant SKCA-BR 11 4623793 4623793 single base substitution T C upstream_gene_variant SKCA-BR 11 4624929 4624929 single base substitution G A intron_variant SKCA-BR 11 4624929 4624929 single base substitution G A upstream_gene_variant SKCA-BR 11 4625578 4625578 single base substitution C T intron_variant SKCA-BR 11 4625578 4625578 single base substitution C T upstream_gene_variant SKCA-BR 11 4629284 4629284 single base substitution C T 5_prime_UTR_variant SKCA-BR 11 4629284 4629284 single base substitution C T exon_variant SKCA-BR 11 4630044 4630044 single base substitution A C upstream_gene_variant SKCA-BR 11 4631430 4631430 single base substitution G A upstream_gene_variant SKCA-BR 11 4631978 4631978 single base substitution G A upstream_gene_variant SKCA-BR 11 4632979 4632979 single base substitution A T upstream_gene_variant SKCA-BR 11 4633788 4633788 single base substitution G A upstream_gene_variant SKCM-US 11 4615299 4615299 single base substitution G A downstream_gene_variant SKCM-US 11 4615303 4615303 single base substitution C T downstream_gene_variant SKCM-US 11 4615434 4615434 single base substitution G A downstream_gene_variant SKCM-US 11 4615507 4615507 single base substitution C T downstream_gene_variant SKCM-US 11 4615509 4615509 single base substitution G A downstream_gene_variant SKCM-US 11 4615877 4615877 single base substitution T A downstream_gene_variant SKCM-US 11 4616183 4616183 single base substitution G A downstream_gene_variant SKCM-US 11 4616188 4616188 single base substitution G A downstream_gene_variant SKCM-US 11 4616195 4616195 single base substitution G A downstream_gene_variant SKCM-US 11 4621530 4621530 single base substitution G A 3_prime_UTR_variant SKCM-US 11 4621530 4621530 single base substitution G A downstream_gene_variant SKCM-US 11 4621530 4621530 single base substitution G A synonymous_variant I478I 1434C>T SKCM-US 11 4621703 4621703 single base substitution G A 3_prime_UTR_variant SKCM-US 11 4621703 4621703 single base substitution G A downstream_gene_variant SKCM-US 11 4621703 4621703 single base substitution G A missense_variant R421C 1261C>T SKCM-US 11 4621725 4621725 single base substitution G A 3_prime_UTR_variant SKCM-US 11 4621725 4621725 single base substitution G A downstream_gene_variant SKCM-US 11 4621725 4621725 single base substitution G A synonymous_variant I413I 1239C>T SKCM-US 11 4621926 4621926 single base substitution G A 3_prime_UTR_variant SKCM-US 11 4621926 4621926 single base substitution G A downstream_gene_variant SKCM-US 11 4621926 4621926 single base substitution G A synonymous_variant I123I 369C>T SKCM-US 11 4621926 4621926 single base substitution G A synonymous_variant I346I 1038C>T SKCM-US 11 4622013 4622013 single base substitution G A 3_prime_UTR_variant SKCM-US 11 4622013 4622013 single base substitution G A downstream_gene_variant SKCM-US 11 4622013 4622013 single base substitution G A synonymous_variant I317I 951C>T SKCM-US 11 4622013 4622013 single base substitution G A synonymous_variant I94I 282C>T SKCM-US 11 4626489 4626489 single base substitution G A exon_variant SKCM-US 11 4626489 4626489 single base substitution G A intron_variant SKCM-US 11 4626489 4626489 single base substitution G A synonymous_variant V82V 246C>T SKCM-US 11 4626489 4626489 single base substitution G A upstream_gene_variant SKCM-US 11 4626492 4626492 deletion of <=200bp T - exon_variant SKCM-US 11 4626492 4626492 deletion of <=200bp T - frameshift_variant K81 SKCM-US 11 4626492 4626492 deletion of <=200bp T - intron_variant SKCM-US 11 4626492 4626492 deletion of <=200bp T - upstream_gene_variant STAD-US 11 4615541 4615541 single base substitution G A downstream_gene_variant STAD-US 11 4615836 4615836 single base substitution A G downstream_gene_variant STAD-US 11 4615839 4615839 single base substitution T G downstream_gene_variant STAD-US 11 4615865 4615865 single base substitution C A downstream_gene_variant STAD-US 11 4621595 4621595 single base substitution G A 3_prime_UTR_variant STAD-US 11 4621595 4621595 single base substitution G A downstream_gene_variant STAD-US 11 4621595 4621595 single base substitution G A missense_variant R457C 1369C>T STAD-US 11 4621672 4621672 single base substitution G A 3_prime_UTR_variant STAD-US 11 4621672 4621672 single base substitution G A downstream_gene_variant STAD-US 11 4621672 4621672 single base substitution G A missense_variant A431V 1292C>T STAD-US 11 4621678 4621678 single base substitution T C 3_prime_UTR_variant STAD-US 11 4621678 4621678 single base substitution T C downstream_gene_variant STAD-US 11 4621678 4621678 single base substitution T C missense_variant Y429C 1286A>G STAD-US 11 4621712 4621712 single base substitution C A 3_prime_UTR_variant STAD-US 11 4621712 4621712 single base substitution C A downstream_gene_variant STAD-US 11 4621712 4621712 single base substitution C A missense_variant V418F 1252G>T STAD-US 11 4621714 4621714 single base substitution G A 3_prime_UTR_variant STAD-US 11 4621714 4621714 single base substitution G A downstream_gene_variant STAD-US 11 4621714 4621714 single base substitution G A missense_variant P417L 1250C>T STAD-US 11 4621796 4621796 deletion of <=200bp G - 3_prime_UTR_variant STAD-US 11 4621796 4621796 deletion of <=200bp G - downstream_gene_variant STAD-US 11 4621796 4621796 deletion of <=200bp G - frameshift_variant H390 STAD-US 11 4621846 4621846 single base substitution C A 3_prime_UTR_variant STAD-US 11 4621846 4621846 single base substitution C A downstream_gene_variant STAD-US 11 4621846 4621846 single base substitution C A missense_variant G373V 1118G>T STAD-US 11 4621976 4621976 single base substitution T C 3_prime_UTR_variant STAD-US 11 4621976 4621976 single base substitution T C downstream_gene_variant STAD-US 11 4621976 4621976 single base substitution T C missense_variant T107A 319A>G STAD-US 11 4621976 4621976 single base substitution T C missense_variant T330A 988A>G STAD-US 11 4622048 4622048 single base substitution G A 3_prime_UTR_variant STAD-US 11 4622048 4622048 single base substitution G A downstream_gene_variant STAD-US 11 4622048 4622048 single base substitution G A exon_variant STAD-US 11 4622048 4622048 single base substitution G A missense_variant R306C 916C>T STAD-US 11 4622048 4622048 single base substitution G A missense_variant R83C 247C>T STAD-US 11 4622295 4622295 single base substitution C G 3_prime_UTR_variant STAD-US 11 4622295 4622295 single base substitution C G downstream_gene_variant STAD-US 11 4622295 4622295 single base substitution C G exon_variant STAD-US 11 4622295 4622295 single base substitution C G missense_variant R290P 869G>C STAD-US 11 4622295 4622295 single base substitution C G missense_variant R67P 200G>C UCEC-US 11 4615989 4615989 single base substitution G T downstream_gene_variant UCEC-US 11 4616176 4616176 single base substitution A G downstream_gene_variant UCEC-US 11 4621686 4621686 single base substitution G A 3_prime_UTR_variant UCEC-US 11 4621686 4621686 single base substitution G A downstream_gene_variant UCEC-US 11 4621686 4621686 single base substitution G A synonymous_variant F426F 1278C>T UCEC-US 11 4621715 4621715 single base substitution G A 3_prime_UTR_variant UCEC-US 11 4621715 4621715 single base substitution G A downstream_gene_variant UCEC-US 11 4621715 4621715 single base substitution G A missense_variant P417S 1249C>T UCEC-US 11 4621922 4621922 single base substitution G A 3_prime_UTR_variant UCEC-US 11 4621922 4621922 single base substitution G A downstream_gene_variant UCEC-US 11 4621922 4621922 single base substitution G A synonymous_variant L125L 373C>T UCEC-US 11 4621922 4621922 single base substitution G A synonymous_variant L348L 1042C>T UCEC-US 11 4626532 4626532 single base substitution T C exon_variant UCEC-US 11 4626532 4626532 single base substitution T C intron_variant UCEC-US 11 4626532 4626532 single base substitution T C missense_variant N68S 203A>G UCEC-US 11 4626532 4626532 single base substitution T C upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand S00833 COSM316170 c.248G>A p.R83H Substitution - Missense 11:4605257-4605257 - HCC96T COSM3666321 c.384C>G p.A128A Substitution - coding silent 11:4605121-4605121 - TCGA-AA-3666-01 COSM292672 c.1038C>T p.I346I Substitution - coding silent 11:4600696-4600696 - YUKADI COSM1703370 c.304_305GG>AA p.G102K Substitution - Missense 11:4605200-4605201 - TCGA-CD-A4MG-01 COSM4032961 c.1286A>G p.Y429C Substitution - Missense 11:4600448-4600448 - UM-SCC-17B COSM4593832 c.1325G>A p.C442Y Substitution - Missense 11:4600409-4600409 - TCGA-HU-A4GX-01 COSM4032966 c.916C>T p.R306C Substitution - Missense 11:4600818-4600818 - PD4261a COSM5771414 c.970C>T p.R324C Substitution - Missense 11:4600764-4600764 - TCGA-66-2791-01 COSM688074 c.1194G>A p.L398L Substitution - coding silent 11:4600540-4600540 - HCC96 COSM3666321 c.384C>G p.A128A Substitution - coding silent 11:4605121-4605121 - 2497767 COSM3676159 c.952G>A p.V318M Substitution - Missense 11:4600782-4600782 - CSCC-15-T COSM4481051 c.247C>T p.R83C Substitution - Missense 11:4605258-4605258 - 8064632 COSM1734617 c.519G>T p.W173C Substitution - Missense 11:4603248-4603248 - 16 COSM3735412 c.769C>T p.R257C Substitution - Missense 11:4602166-4602166 - P50 COSM328928 c.1399A>G p.S467G Substitution - Missense 11:4600335-4600335 - TCGA-EE-A29E-06 COSM3447520 c.1261C>T p.R421C Substitution - Missense 11:4600473-4600473 - ESCC-078T COSM3935472 c.759G>A p.Q253Q Substitution - coding silent 11:4602176-4602176 - TCGA-A8-A09R-01 COSM429003 c.1279G>A p.V427M Substitution - Missense 11:4600455-4600455 - CHC892T COSM4794374 c.366G>A p.Q122Q Substitution - coding silent 11:4605139-4605139 - TCGA-EE-A181-06 COSM3447523 c.246C>T p.V82V Substitution - coding silent 11:4605259-4605259 - 2290930 COSM4440307 c.839C>A p.P280Q Substitution - Missense 11:4601095-4601095 - TCGA-CD-A4MI-01 COSM4032962 c.1252G>T p.V418F Substitution - Missense 11:4600482-4600482 - CAL27 COSM4593832 c.1325G>A p.C442Y Substitution - Missense 11:4600409-4600409 - TCGA-BR-4201-01 COSM4032963 c.1250C>T p.P417L Substitution - Missense 11:4600484-4600484 - TCGA-P4-A5EA-01 COSM3986174 c.1214G>A p.R405Q Substitution - Missense 11:4600520-4600520 - TCGA-BR-6452-01 COSM4032964 c.1118G>T p.G373V Substitution - Missense 11:4600616-4600616 - CHC892T COSM4794374 c.366G>A p.Q122Q Substitution - coding silent 11:4605139-4605139 - LIM2551 COSM4643540 c.910G>A p.D304N Substitution - Missense 11:4600824-4600824 - TCGA-JX-A3Q0-01 COSM4824434 c.697G>A p.E233K Substitution - Missense 11:4602238-4602238 - TCGA-BS-A0UV-01 COSM927132 c.1278C>T p.F426F Substitution - coding silent 11:4600456-4600456 - 587220 COSM1230401 c.547A>G p.S183G Substitution - Missense 11:4602388-4602388 - CSCC-56-T COSM4454731 c.568A>T p.K190* Substitution - Nonsense 11:4602367-4602367 - LP6005334-DNA_D03 COSM5953172 c.1092G>A p.V364V Substitution - coding silent 11:4600642-4600642 - tumor_4163639 COSM1160989 c.767T>C p.V256A Substitution - Missense 11:4602168-4602168 - ESCC_25 COSM5626577 c.723G>C p.L241L Substitution - coding silent 11:4602212-4602212 - TCGA-A6-3807-01 COSM291308 c.815C>T p.S272F Substitution - Missense 11:4601119-4601119 - 8057574 COSM3383485 c.732G>A p.M244I Substitution - Missense 11:4602203-4602203 - RK064_C01 COSM1627984 c.807-10C>G p.? Unknown 11:4601137-4601137 - TCGA-F4-6856-01 COSM1353875 c.299G>A p.R100H Substitution - Missense 11:4605206-4605206 - TCGA-AP-A059-01 COSM927135 c.203A>G p.N68S Substitution - Missense 11:4605302-4605302 - pfg145T COSM4749051 c.800T>C p.L267S Substitution - Missense 11:4601670-4601670 - TCGA-D3-A51G-06 COSM3447522 c.951C>T p.I317I Substitution - coding silent 11:4600783-4600783 - YUGOE COSM1703371 c.173C>T p.P58L Substitution - Missense 11:4605332-4605332 - ACINAR01 COSM1734615 c.653G>A p.R218Q Substitution - Missense 11:4602282-4602282 - 587376 COSM1230403 c.790C>A p.Q264K Substitution - Missense 11:4601680-4601680 - S02255 COSM5680402 c.207G>A p.L69L Substitution - coding silent 11:4605298-4605298 - Pat_06_B COSM4032959 c.1369C>T p.R457C Substitution - Missense 11:4600365-4600365 - TCGA-BR-4361-01 COSM4032965 c.988A>G p.T330A Substitution - Missense 11:4600746-4600746 - ATL037 COSM5704010 c.1415A>G p.N472S Substitution - Missense 11:4600319-4600319 - Pat_59_B COSM5838573 c.1343C>T p.T448I Substitution - Missense 11:4600391-4600391 - CSCC-27-T COSM4466262 c.1424C>A p.P475H Substitution - Missense 11:4600310-4600310 - S00833 COSM316170 c.248G>A p.R83H Substitution - Missense 11:4605257-4605257 - ESCC_BICR_070T COSM5444819 c.1105G>C p.E369Q Substitution - Missense 11:4600629-4600629 - TCGA-FD-A3SJ-01 COSM3791494 c.622G>A p.E208K Substitution - Missense 11:4602313-4602313 - LUAD-CHTN-Z4716A COSM361539 c.929A>T p.D310V Substitution - Missense 11:4600805-4600805 - TCGA-DD-A3A8-01 COSM1508243 c.1070G>A p.R357Q Substitution - Missense 11:4600664-4600664 - TCGA-EJ-7328-01 COSM316170 c.248G>A p.R83H Substitution - Missense 11:4605257-4605257 - 1N45-VS-1T45 COSM4975748 c.145G>T p.E49* Substitution - Nonsense 11:4605360-4605360 - TCGA-AA-3672-01 COSM267638 c.298C>T p.R100C Substitution - Missense 11:4605207-4605207 - TCGA-BR-8680-01 COSM4032960 c.1292C>T p.A431V Substitution - Missense 11:4600442-4600442 - CCK81 COSM1980060 c.1188A>G p.I396M Substitution - Missense 11:4600546-4600546 - TCGA-24-1545-01 COSM78701 c.944G>A p.R315H Substitution - Missense 11:4600790-4600790 - TCGA-AZ-6598-01 COSM1353870 c.1027C>T p.R343C Substitution - Missense 11:4600707-4600707 - TCGA-BG-A18B-01 COSM927134 c.1042C>T p.L348L Substitution - coding silent 11:4600692-4600692 - B74 COSM1746232 c.1383T>A p.Y461* Substitution - Nonsense 11:4600351-4600351 - S02299 COSM5690051 c.326G>T p.C109F Substitution - Missense 11:4605179-4605179 - sysucc-1317T COSM1353875 c.299G>A p.R100H Substitution - Missense 11:4605206-4605206 - HT115 COSM1353870 c.1027C>T p.R343C Substitution - Missense 11:4600707-4600707 - TCGA-IH-A3EA-01 COSM3447520 c.1261C>T p.R421C Substitution - Missense 11:4600473-4600473 - LIM2551 COSM4643539 c.1113C>G p.G371G Substitution - coding silent 11:4600621-4600621 - SJACT02_D COSM4968364 c.616G>T p.G206W Substitution - Missense 11:4602319-4602319 - TCGA-A2-A0EQ-01 COSM429004 c.315G>A p.L105L Substitution - coding silent 11:4605190-4605190 - YUKAT COSM5372500 c.1061C>T p.S354F Substitution - Missense 11:4600673-4600673 - H322T COSM1194840 c.1283A>C p.D428A Substitution - Missense 11:4600451-4600451 - 8031146 COSM1168722 c.403G>A p.E135K Substitution - Missense 11:4605102-4605102 - TCGA-AG-3592-01 COSM3415876 c.862G>C p.D288H Substitution - Missense 11:4601072-4601072 - ACINAR18 COSM1734617 c.519G>T p.W173C Substitution - Missense 11:4603248-4603248 - TCGA-18-3412-01 COSM688073 c.439G>A p.E147K Substitution - Missense 11:4603328-4603328 - ESO-0025 COSM1268575 c.1351C>T p.R451C Substitution - Missense 11:4600383-4600383 - 587342 COSM1230402 c.1039G>A p.V347I Substitution - Missense 11:4600695-4600695 - TCGA-G4-6586-01 COSM1353868 c.1168delC p.H390fs*6 Deletion - Frameshift 11:4600566-4600566 - TCGA-EE-A20H-06 COSM3447521 c.1239C>T p.I413I Substitution - coding silent 11:4600495-4600495 - TCGA-AX-A0J1-01 COSM927133 c.1249C>T p.P417S Substitution - Missense 11:4600485-4600485 - TCGA-DA-A1HV-06 COSM3447519 c.1434C>T p.I478I Substitution - coding silent 11:4600300-4600300 - Gp5D COSM1980082 c.372A>G p.P124P Substitution - coding silent 11:4605133-4605133 - SNUH_G47_S1 COSM3676159 c.952G>A p.V318M Substitution - Missense 11:4600782-4600782 - SNU-C2B COSM1980072 c.770G>A p.R257H Substitution - Missense 11:4602165-4602165 - H1703 COSM1196664 c.1426C>G p.L476V Substitution - Missense 11:4600308-4600308 - 35M COSM5582857 c.1362C>T p.F454F Substitution - coding silent 11:4600372-4600372 - TCGA-E6-A1LZ-01 COSM927136 c.37G>A p.E13K Substitution - Missense 11:4605468-4605468 - TCGA-37-4133-01 COSM688072 c.68T>A p.L23Q Substitution - Missense 11:4605437-4605437 - 35M COSM5582856 c.7C>T p.P3S Substitution - Missense 11:4605498-4605498 - TCGA-BQ-7061-01 COSM3986175 c.1030T>C p.Y344H Substitution - Missense 11:4600704-4600704 - KM12 COSM1980055 c.1398C>T p.Y466Y Substitution - coding silent 11:4600336-4600336 - CHC1534T COSM4955082 c.460A>T p.K154* Substitution - Nonsense 11:4603307-4603307 - TCGA-DB-5277-01 COSM3967518 c.119T>C p.L40P Substitution - Missense 11:4605386-4605386 - T3090 COSM4736216 c.992A>G p.N331S Substitution - Missense 11:4600742-4600742 - UM-SCC-47 COSM4593832 c.1325G>A p.C442Y Substitution - Missense 11:4600409-4600409 - 587376 COSM1230404 c.290T>C p.L97P Substitution - Missense 11:4605215-4605215 - H1155 COSM1195290 c.652C>T p.R218W Substitution - Missense 11:4602283-4602283 - Gp2D COSM1980082 c.372A>G p.P124P Substitution - coding silent 11:4605133-4605133 - TCGA-C4-A0EZ-01 COSM415602 c.132G>A p.W44* Substitution - Nonsense 11:4605373-4605373 - RK308_C01 COSM3739058 c.1191G>A p.R397R Substitution - coding silent 11:4600543-4600543 - 206T COSM1726879 c.985G>C p.D329H Substitution - Missense 11:4600749-4600749 - HCC136T COSM5817172 c.1194G>T p.L398L Substitution - coding silent 11:4600540-4600540 - TCGA-BR-A4PF-01 COSM4032967 c.869G>C p.R290P Substitution - Missense 11:4601065-4601065 - C008 COSM5524087 c.188C>T p.P63L Substitution - Missense 11:4605317-4605317 - 2521259 COSM5890663 c.172C>T p.P58S Substitution - Missense 11:4605333-4605333 - TCGA-EE-A2MR-06 COSM292672 c.1038C>T p.I346I Substitution - coding silent 11:4600696-4600696 - HT115 COSM1980078 c.506G>A p.R169Q Substitution - Missense 11:4603261-4603261 - TCGA-BR-8361-01 COSM4032959 c.1369C>T p.R457C Substitution - Missense 11:4600365-4600365 - CHC1534T COSM4955082 c.460A>T p.K154* Substitution - Nonsense 11:4603307-4603307 - PT49 COSM5935813 c.118C>T p.L40F Substitution - Missense 11:4605387-4605387 - TCGA-CF-A3MI-01 COSM1298055 c.1194G>C p.L398L Substitution - coding silent 11:4600540-4600540 - T2940 COSM1353870 c.1027C>T p.R343C Substitution - Missense 11:4600707-4600707 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.523432;Hs.523438 11p15.4 613184

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G IntronicSNV . c.784-16T>C 11 4622932 ESCA A G Missense p.L40P c.119T>C 11 4626616 LGG A G Missense p.V256A c.767T>C 11 4623398 DLBCL A T Missense p.L23Q c.68T>A 11 4626667 LUSC C A Missense p.R422L c.1265G>T 11 4621699 STAD C A Synonymous p.R381R c.1143G>T 11 4621821 CM C G Missense p.E140D c.420G>C 11 4626315 HNSC C G Missense p.V374L c.1120G>C 11 4621844 HNSC C G Synonymous p.L398L c.1194G>C 11 4621770 BLCA C T IntronicSNV . c.806+122G>A 11 4622772 CM C T Missense p.E147K c.439G>A 11 4624558 LUSC C T Missense p.R315H c.944G>A 11 4622020 OV C T Missense p.R83H c.248G>A 11 4626487 PRAD C T Missense p.R83H c.248G>A 11 4626487 SCLC C T Missense p.V427M c.1279G>A 11 4621685 BRCA C T Missense p.V439M c.1315G>A 11 4621649 STAD C T Nonsense p.W44* c.132G>A 11 4626603 BLCA C T Synonymous p.L105L c.315G>A 11 4626420 BRCA C T Synonymous p.L229L c.687G>A 11 4623478 LUAD C T Synonymous p.L398L c.1194G>A 11 4621770 LUSC G A IntronicSNV . c.806+172C>T 11 4622722 CM G A Missense p.P417L c.1250C>T 11 4621714 STAD G A Missense p.P464S c.1390C>T 11 4621574 CM G A Missense p.R421C c.1261C>T 11 4621703 CM G A Missense p.S272F c.815C>T 11 4622349 COREAD G A Synonymous p.I346I c.1038C>T 11 4621926 CM G A Synonymous p.I346I c.1038C>T 11 4621926 COREAD G A Synonymous p.I413I c.1239C>T 11 4621725 CM G A Synonymous p.I478I c.1434C>T 11 4621530 CM G A Synonymous p.L348L c.1042C>T 11 4621922 UCEC G A Synonymous p.V82V c.246C>T 11 4626489 CM G C Missense p.S272C c.815C>G 11 4622349 HNSC T A SpliceAcceptorSNV . c.1-59A>T 11 4626793 SCLC T C Missense p.Y391C c.1172A>G 11 4621792 HNSC T - Frameshift p.V82Sfs*4 c.243delA 11 4626492 CM