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 12 6958797 6958797 + Missense_Mutation SNP G G T TCGA-XF-A9SK-01A-11D-A42E-08 TCGA-XF-A9SK-10A-01D-A42H-08 g.chr12:6958797G>T c.476C>A c.(475-477)aCa>aAa p.T159K BLCA 12 6958960 6958960 + Missense_Mutation SNP T T C TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr12:6958960T>C c.313A>G c.(313-315)Aat>Gat p.N105D BLCA 12 6958994 6958994 + Silent SNP C C T TCGA-HQ-A2OE-01A-11D-A202-08 TCGA-HQ-A2OE-10A-01D-A202-08 g.chr12:6958994C>T c.279G>A c.(277-279)ctG>ctA p.L93L BLCA 12 6959647 6959647 + Missense_Mutation SNP C C T TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chr12:6959647C>T c.234G>A c.(232-234)atG>atA p.M78I BRCA 12 6958758 6958758 + Missense_Mutation SNP G G A TCGA-A8-A094-01A-11W-A019-09 TCGA-A8-A094-10A-01W-A021-09 g.chr12:6958758G>A c.515C>T c.(514-516)tCa>tTa p.S172L CESC 12 6958994 6958994 + Silent SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr12:6958994C>G c.279G>C c.(277-279)ctG>ctC p.L93L COAD 12 6958356 6958356 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr12:6958356G>A c.658C>T c.(658-660)Cgg>Tgg p.R220W COAD 12 6959019 6959019 + Missense_Mutation SNP G G T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr12:6959019G>T c.254C>A c.(253-255)cCc>cAc p.P85H COADREAD 12 6958266 6958266 + Missense_Mutation SNP A A G TCGA-AG-A036-01A-12W-A096-10 TCGA-AG-A036-11A-11W-A096-10 g.chr12:6958266A>G c.748T>C c.(748-750)Tgg>Cgg p.W250R COADREAD 12 6958356 6958356 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr12:6958356G>A c.658C>T c.(658-660)Cgg>Tgg p.R220W COADREAD 12 6958846 6958846 + Missense_Mutation SNP C C G TCGA-AG-3881-01A-01W-0899-10 TCGA-AG-3881-10A-01W-0901-10 g.chr12:6958846C>G c.427G>C c.(427-429)Gag>Cag p.E143Q COADREAD 12 6959019 6959019 + Missense_Mutation SNP G G T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr12:6959019G>T c.254C>A c.(253-255)cCc>cAc p.P85H GBM 12 6959664 6959664 + Missense_Mutation SNP T T C TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chr12:6959664T>C c.217A>G c.(217-219)Att>Gtt p.I73V GBMLGG 12 6958590 6958590 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr12:6958590G>T c.548C>A c.(547-549)tCt>tAt p.S183Y GBMLGG 12 6959664 6959664 + Missense_Mutation SNP T T C TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chr12:6959664T>C c.217A>G c.(217-219)Att>Gtt p.I73V HNSC 12 6958258 6958258 + Silent SNP T T C TCGA-BA-4078-01A-01D-1434-08 TCGA-BA-4078-10A-01D-1434-08 g.chr12:6958258T>C c.756A>G c.(754-756)caA>caG p.Q252Q LGG 12 6958590 6958590 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr12:6958590G>T c.548C>A c.(547-549)tCt>tAt p.S183Y LIHC 12 6958537 6958537 + Frame_Shift_Del DEL G G - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr12:6958537delG c.601delC c.(601-603)ctcfs p.L201fs LUAD 12 6958844 6958844 + Missense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr12:6958844C>A c.429G>T c.(427-429)gaG>gaT p.E143D LUAD 12 6959654 6959654 + Missense_Mutation SNP G G T TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr12:6959654G>T c.227C>A c.(226-228)aCa>aAa p.T76K PAAD 12 6958344 6958344 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr12:6958344G>A c.670C>T c.(670-672)Cta>Tta p.L224L PRAD 12 6958354 6958354 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr12:6958354C>T c.660G>A c.(658-660)cgG>cgA p.R220R PRAD 12 6958585 6958585 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr12:6958585G>A c.553C>T c.(553-555)Cgc>Tgc p.R185C READ 12 6958266 6958266 + Missense_Mutation SNP A A G TCGA-AG-A036-01A-12W-A096-10 TCGA-AG-A036-11A-11W-A096-10 g.chr12:6958266A>G c.748T>C c.(748-750)Tgg>Cgg p.W250R READ 12 6958846 6958846 + Missense_Mutation SNP C C G TCGA-AG-3881-01A-01W-0899-10 TCGA-AG-3881-10A-01W-0901-10 g.chr12:6958846C>G c.427G>C c.(427-429)Gag>Cag p.E143Q SARC 12 6959716 6959716 + Silent SNP C C A TCGA-X6-A7WC-01A-12D-A351-09 TCGA-X6-A7WC-10A-01D-A351-09 g.chr12:6959716C>A c.165G>T c.(163-165)ctG>ctT p.L55L SKCM 12 6958754 6958754 + Silent SNP C C T TCGA-D3-A1Q1-06A-21D-A196-08 TCGA-D3-A1Q1-10A-01D-A198-08 g.chr12:6958754C>T c.519G>A c.(517-519)agG>agA p.R173R SKCM 12 6958788 6958788 + Missense_Mutation SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr12:6958788G>A c.485C>T c.(484-486)cCt>cTt p.P162L SKCM 12 6958951 6958951 + Missense_Mutation SNP G G A TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr12:6958951G>A c.322C>T c.(322-324)Cca>Tca p.P108S

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 12 6964621 6964621 single base substitution G T upstream_gene_variant BLCA-US 12 6952355 6952355 single base substitution C T downstream_gene_variant BLCA-US 12 6954828 6954828 single base substitution G A 3_prime_UTR_variant BLCA-US 12 6954828 6954828 single base substitution G A downstream_gene_variant BLCA-US 12 6954828 6954828 single base substitution G A exon_variant BLCA-US 12 6954874 6954874 single base substitution C G 3_prime_UTR_variant BLCA-US 12 6954874 6954874 single base substitution C G downstream_gene_variant BLCA-US 12 6954874 6954874 single base substitution C G exon_variant BLCA-US 12 6958994 6958994 single base substitution C T downstream_gene_variant BLCA-US 12 6958994 6958994 single base substitution C T exon_variant BLCA-US 12 6958994 6958994 single base substitution C T intron_variant BLCA-US 12 6958994 6958994 single base substitution C T synonymous_variant L93L 279G>A BLCA-US 12 6958994 6958994 single base substitution C T upstream_gene_variant BLCA-US 12 6959647 6959647 single base substitution C T exon_variant BLCA-US 12 6959647 6959647 single base substitution C T missense_variant M78I 234G>A BLCA-US 12 6959647 6959647 single base substitution C T upstream_gene_variant BRCA-EU 12 6951552 6951552 insertion of <=200bp - A downstream_gene_variant BRCA-EU 12 6951775 6951775 single base substitution C T downstream_gene_variant BRCA-EU 12 6952112 6952112 single base substitution T G downstream_gene_variant BRCA-EU 12 6952590 6952590 single base substitution T A downstream_gene_variant BRCA-EU 12 6954133 6954133 single base substitution C A 3_prime_UTR_variant BRCA-EU 12 6954133 6954133 single base substitution C A downstream_gene_variant BRCA-EU 12 6954133 6954133 single base substitution C A exon_variant BRCA-EU 12 6954272 6954272 single base substitution T A 3_prime_UTR_variant BRCA-EU 12 6954272 6954272 single base substitution T A downstream_gene_variant BRCA-EU 12 6954272 6954272 single base substitution T A exon_variant BRCA-EU 12 6954511 6954511 single base substitution G A 3_prime_UTR_variant BRCA-EU 12 6954511 6954511 single base substitution G A downstream_gene_variant BRCA-EU 12 6954511 6954511 single base substitution G A exon_variant BRCA-EU 12 6954739 6954739 single base substitution C A 3_prime_UTR_variant BRCA-EU 12 6954739 6954739 single base substitution C A downstream_gene_variant BRCA-EU 12 6954739 6954739 single base substitution C A exon_variant BRCA-EU 12 6955219 6955219 single base substitution C T 3_prime_UTR_variant BRCA-EU 12 6955219 6955219 single base substitution C T downstream_gene_variant BRCA-EU 12 6955219 6955219 single base substitution C T exon_variant BRCA-EU 12 6955510 6955510 single base substitution C A 3_prime_UTR_variant BRCA-EU 12 6955510 6955510 single base substitution C A downstream_gene_variant BRCA-EU 12 6955510 6955510 single base substitution C A exon_variant BRCA-EU 12 6957247 6957247 single base substitution C T downstream_gene_variant BRCA-EU 12 6957247 6957247 single base substitution C T exon_variant BRCA-EU 12 6957247 6957247 single base substitution C T intron_variant BRCA-EU 12 6957784 6957784 single base substitution G C downstream_gene_variant BRCA-EU 12 6957784 6957784 single base substitution G C exon_variant BRCA-EU 12 6957784 6957784 single base substitution G C intron_variant BRCA-EU 12 6957784 6957784 single base substitution G C upstream_gene_variant BRCA-EU 12 6958174 6958174 single base substitution C A 3_prime_UTR_variant BRCA-EU 12 6958174 6958174 single base substitution C A downstream_gene_variant BRCA-EU 12 6958174 6958174 single base substitution C A exon_variant BRCA-EU 12 6958174 6958174 single base substitution C A intron_variant BRCA-EU 12 6958174 6958174 single base substitution C A upstream_gene_variant BRCA-EU 12 6959444 6959444 single base substitution C T exon_variant BRCA-EU 12 6959444 6959444 single base substitution C T intron_variant BRCA-EU 12 6959444 6959444 single base substitution C T upstream_gene_variant BRCA-EU 12 6960377 6960377 single base substitution A T 5_prime_UTR_variant BRCA-EU 12 6960377 6960377 single base substitution A T intron_variant BRCA-EU 12 6960377 6960377 single base substitution A T upstream_gene_variant BRCA-EU 12 6960586 6960586 single base substitution T G 5_prime_UTR_variant BRCA-EU 12 6960586 6960586 single base substitution T G upstream_gene_variant BRCA-EU 12 6961357 6961357 single base substitution G C upstream_gene_variant BRCA-EU 12 6963388 6963388 single base substitution G T upstream_gene_variant BRCA-EU 12 6963929 6963929 single base substitution T A upstream_gene_variant BRCA-EU 12 6965135 6965135 single base substitution C T upstream_gene_variant BRCA-FR 12 6951775 6951775 single base substitution C T downstream_gene_variant BRCA-FR 12 6952590 6952590 single base substitution T A downstream_gene_variant BRCA-US 12 6952161 6952161 single base substitution C T downstream_gene_variant BRCA-US 12 6952186 6952186 single base substitution C T downstream_gene_variant BRCA-US 12 6955960 6955960 single base substitution C T downstream_gene_variant BRCA-US 12 6955960 6955960 single base substitution C T exon_variant BRCA-US 12 6955960 6955960 single base substitution C T missense_variant D218N 652G>A BRCA-US 12 6958719 6958719 single base substitution G T downstream_gene_variant BRCA-US 12 6958719 6958719 single base substitution G T exon_variant BRCA-US 12 6958719 6958719 single base substitution G T intron_variant BRCA-US 12 6958719 6958719 single base substitution G T upstream_gene_variant BRCA-US 12 6958758 6958758 single base substitution G A downstream_gene_variant BRCA-US 12 6958758 6958758 single base substitution G A exon_variant BRCA-US 12 6958758 6958758 single base substitution G A missense_variant S147L 440C>T BRCA-US 12 6958758 6958758 single base substitution G A missense_variant S172L 515C>T BRCA-US 12 6958758 6958758 single base substitution G A upstream_gene_variant BRCA-US 12 6961446 6961446 single base substitution G A upstream_gene_variant BRCA-US 12 6964624 6964624 single base substitution T C upstream_gene_variant BRCA-US 12 6964674 6964674 single base substitution G A upstream_gene_variant BRCA-US 12 6965602 6965602 single base substitution G A upstream_gene_variant BTCA-JP 12 6950752 6950752 single base substitution T C downstream_gene_variant BTCA-JP 12 6951014 6951014 single base substitution G C downstream_gene_variant BTCA-JP 12 6952173 6952173 single base substitution C T downstream_gene_variant BTCA-JP 12 6952452 6952452 single base substitution G A downstream_gene_variant BTCA-JP 12 6954973 6954973 single base substitution G A 3_prime_UTR_variant BTCA-JP 12 6954973 6954973 single base substitution G A downstream_gene_variant BTCA-JP 12 6954973 6954973 single base substitution G A exon_variant BTCA-JP 12 6955852 6955852 single base substitution T C 3_prime_UTR_variant BTCA-JP 12 6955852 6955852 single base substitution T C downstream_gene_variant BTCA-JP 12 6955852 6955852 single base substitution T C exon_variant BTCA-JP 12 6955852 6955852 single base substitution T C intron_variant BTCA-JP 12 6960141 6960141 single base substitution G A 5_prime_UTR_variant BTCA-JP 12 6960141 6960141 single base substitution G A exon_variant BTCA-JP 12 6960141 6960141 single base substitution G A intron_variant BTCA-JP 12 6960141 6960141 single base substitution G A upstream_gene_variant CESC-US 12 6950484 6950484 single base substitution G A downstream_gene_variant CESC-US 12 6954849 6954849 single base substitution G A 3_prime_UTR_variant CESC-US 12 6954849 6954849 single base substitution G A downstream_gene_variant CESC-US 12 6954849 6954849 single base substitution G A exon_variant CESC-US 12 6958094 6958094 single base substitution G A 3_prime_UTR_variant CESC-US 12 6958094 6958094 single base substitution G A downstream_gene_variant CESC-US 12 6958094 6958094 single base substitution G A exon_variant CESC-US 12 6958094 6958094 single base substitution G A intron_variant CESC-US 12 6958094 6958094 single base substitution G A upstream_gene_variant CESC-US 12 6958994 6958994 single base substitution C G downstream_gene_variant CESC-US 12 6958994 6958994 single base substitution C G exon_variant CESC-US 12 6958994 6958994 single base substitution C G intron_variant CESC-US 12 6958994 6958994 single base substitution C G synonymous_variant L93L 279G>C CESC-US 12 6958994 6958994 single base substitution C G upstream_gene_variant COAD-US 12 6950466 6950466 single base substitution G A downstream_gene_variant COAD-US 12 6950768 6950768 single base substitution G A downstream_gene_variant COAD-US 12 6952626 6952626 single base substitution A G downstream_gene_variant COAD-US 12 6954875 6954875 single base substitution C T 3_prime_UTR_variant COAD-US 12 6954875 6954875 single base substitution C T downstream_gene_variant COAD-US 12 6954875 6954875 single base substitution C T exon_variant COAD-US 12 6954898 6954898 single base substitution G A 3_prime_UTR_variant COAD-US 12 6954898 6954898 single base substitution G A downstream_gene_variant COAD-US 12 6954898 6954898 single base substitution G A exon_variant COAD-US 12 6954960 6954960 single base substitution C T 3_prime_UTR_variant COAD-US 12 6954960 6954960 single base substitution C T downstream_gene_variant COAD-US 12 6954960 6954960 single base substitution C T exon_variant COAD-US 12 6964648 6964648 single base substitution C T upstream_gene_variant COAD-US 12 6964655 6964655 single base substitution C T upstream_gene_variant COAD-US 12 6965602 6965602 single base substitution G A upstream_gene_variant COAD-US 12 6965973 6965973 single base substitution C T upstream_gene_variant COCA-CN 12 6952394 6952394 single base substitution C A downstream_gene_variant COCA-CN 12 6952563 6952563 single base substitution A G downstream_gene_variant COCA-CN 12 6952752 6952752 single base substitution C T downstream_gene_variant COCA-CN 12 6953045 6953045 single base substitution C T downstream_gene_variant COCA-CN 12 6954876 6954876 single base substitution G A 3_prime_UTR_variant COCA-CN 12 6954876 6954876 single base substitution G A downstream_gene_variant COCA-CN 12 6954876 6954876 single base substitution G A exon_variant COCA-CN 12 6956008 6956008 single base substitution C T downstream_gene_variant COCA-CN 12 6956008 6956008 single base substitution C T exon_variant COCA-CN 12 6956008 6956008 single base substitution C T missense_variant V202I 604G>A COCA-CN 12 6958755 6958755 single base substitution C A downstream_gene_variant COCA-CN 12 6958755 6958755 single base substitution C A exon_variant COCA-CN 12 6958755 6958755 single base substitution C A missense_variant R148M 443G>T COCA-CN 12 6958755 6958755 single base substitution C A missense_variant R173M 518G>T COCA-CN 12 6958755 6958755 single base substitution C A upstream_gene_variant COCA-CN 12 6958810 6958810 single base substitution C A downstream_gene_variant COCA-CN 12 6958810 6958810 single base substitution C A exon_variant COCA-CN 12 6958810 6958810 single base substitution C A missense_variant A130S 388G>T COCA-CN 12 6958810 6958810 single base substitution C A missense_variant A155S 463G>T COCA-CN 12 6958810 6958810 single base substitution C A upstream_gene_variant COCA-CN 12 6959115 6959115 single base substitution A T downstream_gene_variant COCA-CN 12 6959115 6959115 single base substitution A T intron_variant COCA-CN 12 6959115 6959115 single base substitution A T upstream_gene_variant COCA-CN 12 6964494 6964494 single base substitution G T upstream_gene_variant COCA-CN 12 6965609 6965609 single base substitution T A upstream_gene_variant COCA-CN 12 6965721 6965721 single base substitution G A upstream_gene_variant EOPC-DE 12 6949149 6949149 single base substitution C A downstream_gene_variant EOPC-DE 12 6955030 6955030 single base substitution A C 3_prime_UTR_variant EOPC-DE 12 6955030 6955030 single base substitution A C downstream_gene_variant EOPC-DE 12 6955030 6955030 single base substitution A C exon_variant ESAD-UK 12 6949441 6949441 single base substitution T G downstream_gene_variant ESAD-UK 12 6950272 6950272 single base substitution C T downstream_gene_variant ESAD-UK 12 6952095 6952095 single base substitution A G downstream_gene_variant ESAD-UK 12 6955235 6955235 single base substitution A T 3_prime_UTR_variant ESAD-UK 12 6955235 6955235 single base substitution A T downstream_gene_variant ESAD-UK 12 6955235 6955235 single base substitution A T exon_variant ESAD-UK 12 6957070 6957070 single base substitution G A downstream_gene_variant ESAD-UK 12 6957070 6957070 single base substitution G A intron_variant ESAD-UK 12 6957604 6957604 single base substitution G A downstream_gene_variant ESAD-UK 12 6957604 6957604 single base substitution G A exon_variant ESAD-UK 12 6957604 6957604 single base substitution G A intron_variant ESAD-UK 12 6957604 6957604 single base substitution G A upstream_gene_variant ESAD-UK 12 6961356 6961356 single base substitution A G upstream_gene_variant ESAD-UK 12 6962737 6962737 single base substitution A G upstream_gene_variant ESAD-UK 12 6964998 6964998 single base substitution G T upstream_gene_variant ESAD-UK 12 6965094 6965094 single base substitution G A upstream_gene_variant ESCA-CN 12 6956462 6956462 single base substitution C T downstream_gene_variant ESCA-CN 12 6956462 6956462 single base substitution C T intron_variant ESCA-CN 12 6959682 6959682 single base substitution G A exon_variant ESCA-CN 12 6959682 6959682 single base substitution G A missense_variant R67C 199C>T ESCA-CN 12 6959682 6959682 single base substitution G A upstream_gene_variant GBM-US 12 6959664 6959664 single base substitution T C exon_variant GBM-US 12 6959664 6959664 single base substitution T C missense_variant I73V 217A>G GBM-US 12 6959664 6959664 single base substitution T C upstream_gene_variant LAML-KR 12 6965740 6965740 single base substitution C A upstream_gene_variant LICA-CN 12 6958769 6958769 single base substitution G A downstream_gene_variant LICA-CN 12 6958769 6958769 single base substitution G A exon_variant LICA-CN 12 6958769 6958769 single base substitution G A synonymous_variant S143S 429C>T LICA-CN 12 6958769 6958769 single base substitution G A synonymous_variant S168S 504C>T LICA-CN 12 6958769 6958769 single base substitution G A upstream_gene_variant LICA-FR 12 6951071 6951071 single base substitution A C downstream_gene_variant LICA-FR 12 6965575 6965575 single base substitution G A upstream_gene_variant LINC-JP 12 6951129 6951129 single base substitution C T downstream_gene_variant LINC-JP 12 6952089 6952089 single base substitution C A downstream_gene_variant LINC-JP 12 6958874 6958874 single base substitution C T downstream_gene_variant LINC-JP 12 6958874 6958874 single base substitution C T exon_variant LINC-JP 12 6958874 6958874 single base substitution C T synonymous_variant E108E 324G>A LINC-JP 12 6958874 6958874 single base substitution C T synonymous_variant E133E 399G>A LINC-JP 12 6958874 6958874 single base substitution C T upstream_gene_variant LINC-JP 12 6965007 6965009 deletion of <=200bp TTC - upstream_gene_variant LIRI-JP 12 6949380 6949380 single base substitution A G downstream_gene_variant LIRI-JP 12 6954536 6954536 single base substitution C T 3_prime_UTR_variant LIRI-JP 12 6954536 6954536 single base substitution C T downstream_gene_variant LIRI-JP 12 6954536 6954536 single base substitution C T exon_variant LIRI-JP 12 6955563 6955563 single base substitution C A 3_prime_UTR_variant LIRI-JP 12 6955563 6955563 single base substitution C A downstream_gene_variant LIRI-JP 12 6955563 6955563 single base substitution C A exon_variant LIRI-JP 12 6955563 6955563 single base substitution C A intron_variant LIRI-JP 12 6958216 6958216 single base substitution C T 3_prime_UTR_variant LIRI-JP 12 6958216 6958216 single base substitution C T downstream_gene_variant LIRI-JP 12 6958216 6958216 single base substitution C T exon_variant LIRI-JP 12 6958216 6958216 single base substitution C T intron_variant LIRI-JP 12 6958216 6958216 single base substitution C T synonymous_variant V241V 723G>A LIRI-JP 12 6958216 6958216 single base substitution C T synonymous_variant V266V 798G>A LIRI-JP 12 6958216 6958216 single base substitution C T upstream_gene_variant LIRI-JP 12 6964313 6964313 single base substitution G A upstream_gene_variant LIRI-JP 12 6965074 6965074 single base substitution T G upstream_gene_variant LUSC-KR 12 6950992 6950992 single base substitution C G downstream_gene_variant LUSC-KR 12 6956462 6956462 single base substitution C T downstream_gene_variant LUSC-KR 12 6956462 6956462 single base substitution C T intron_variant LUSC-KR 12 6958491 6958491 single base substitution C T downstream_gene_variant LUSC-KR 12 6958491 6958491 single base substitution C T exon_variant LUSC-KR 12 6958491 6958491 single base substitution C T intron_variant LUSC-KR 12 6958491 6958491 single base substitution C T missense_variant R191Q 572G>A LUSC-KR 12 6958491 6958491 single base substitution C T missense_variant R216Q 647G>A LUSC-KR 12 6958491 6958491 single base substitution C T upstream_gene_variant LUSC-KR 12 6959969 6959969 single base substitution C G exon_variant LUSC-KR 12 6959969 6959969 single base substitution C G intron_variant LUSC-KR 12 6959969 6959969 single base substitution C G upstream_gene_variant LUSC-KR 12 6961658 6961658 single base substitution T G upstream_gene_variant LUSC-US 12 6950762 6950762 single base substitution G C downstream_gene_variant LUSC-US 12 6952169 6952169 single base substitution G A downstream_gene_variant LUSC-US 12 6952794 6952794 single base substitution A T downstream_gene_variant LUSC-US 12 6954923 6954923 single base substitution C T 3_prime_UTR_variant LUSC-US 12 6954923 6954923 single base substitution C T downstream_gene_variant LUSC-US 12 6954923 6954923 single base substitution C T exon_variant LUSC-US 12 6964980 6964980 single base substitution C T upstream_gene_variant LUSC-US 12 6965209 6965209 single base substitution G A upstream_gene_variant MALY-DE 12 6949741 6949741 single base substitution C T downstream_gene_variant MALY-DE 12 6950692 6950692 single base substitution C T downstream_gene_variant MALY-DE 12 6961384 6961384 single base substitution C T upstream_gene_variant MELA-AU 12 6949144 6949144 single base substitution G A downstream_gene_variant MELA-AU 12 6949178 6949178 single base substitution A C downstream_gene_variant MELA-AU 12 6949447 6949447 single base substitution C T downstream_gene_variant MELA-AU 12 6950099 6950099 single base substitution G A downstream_gene_variant MELA-AU 12 6950553 6950553 single base substitution G A downstream_gene_variant MELA-AU 12 6950595 6950595 single base substitution C T downstream_gene_variant MELA-AU 12 6950617 6950617 single base substitution G A downstream_gene_variant MELA-AU 12 6951403 6951403 single base substitution G A downstream_gene_variant MELA-AU 12 6952027 6952027 single base substitution G A downstream_gene_variant MELA-AU 12 6952243 6952243 single base substitution G A downstream_gene_variant MELA-AU 12 6953123 6953123 single base substitution C T downstream_gene_variant MELA-AU 12 6953369 6953369 single base substitution A G downstream_gene_variant MELA-AU 12 6953401 6953401 single base substitution G A downstream_gene_variant MELA-AU 12 6953634 6953634 single base substitution G A downstream_gene_variant MELA-AU 12 6953706 6953706 single base substitution C T downstream_gene_variant MELA-AU 12 6954032 6954032 single base substitution G A 3_prime_UTR_variant MELA-AU 12 6954032 6954032 single base substitution G A downstream_gene_variant MELA-AU 12 6954032 6954032 single base substitution G A exon_variant MELA-AU 12 6954993 6954993 single base substitution C T 3_prime_UTR_variant MELA-AU 12 6954993 6954993 single base substitution C T downstream_gene_variant MELA-AU 12 6954993 6954993 single base substitution C T exon_variant MELA-AU 12 6955134 6955134 single base substitution G A 3_prime_UTR_variant MELA-AU 12 6955134 6955134 single base substitution G A downstream_gene_variant MELA-AU 12 6955134 6955134 single base substitution G A exon_variant MELA-AU 12 6955259 6955259 single base substitution G A 3_prime_UTR_variant MELA-AU 12 6955259 6955259 single base substitution G A downstream_gene_variant MELA-AU 12 6955259 6955259 single base substitution G A exon_variant MELA-AU 12 6955568 6955568 single base substitution C T 3_prime_UTR_variant MELA-AU 12 6955568 6955568 single base substitution C T downstream_gene_variant MELA-AU 12 6955568 6955568 single base substitution C T exon_variant MELA-AU 12 6955568 6955568 single base substitution C T intron_variant MELA-AU 12 6955861 6955861 single base substitution A C 3_prime_UTR_variant MELA-AU 12 6955861 6955861 single base substitution A C downstream_gene_variant MELA-AU 12 6955861 6955861 single base substitution A C exon_variant MELA-AU 12 6955861 6955861 single base substitution A C intron_variant MELA-AU 12 6955865 6955865 single base substitution C A 3_prime_UTR_variant MELA-AU 12 6955865 6955865 single base substitution C A downstream_gene_variant MELA-AU 12 6955865 6955865 single base substitution C A exon_variant MELA-AU 12 6955865 6955865 single base substitution C A intron_variant MELA-AU 12 6956476 6956476 single base substitution C T downstream_gene_variant MELA-AU 12 6956476 6956476 single base substitution C T intron_variant MELA-AU 12 6958703 6958703 single base substitution C T downstream_gene_variant MELA-AU 12 6958703 6958703 single base substitution C T exon_variant MELA-AU 12 6958703 6958703 single base substitution C T intron_variant MELA-AU 12 6958703 6958703 single base substitution C T upstream_gene_variant MELA-AU 12 6959146 6959146 single base substitution G A downstream_gene_variant MELA-AU 12 6959146 6959146 single base substitution G A intron_variant MELA-AU 12 6959146 6959146 single base substitution G A upstream_gene_variant MELA-AU 12 6959157 6959157 single base substitution G A downstream_gene_variant MELA-AU 12 6959157 6959157 single base substitution G A intron_variant MELA-AU 12 6959157 6959157 single base substitution G A upstream_gene_variant MELA-AU 12 6959159 6959159 single base substitution A G downstream_gene_variant MELA-AU 12 6959159 6959159 single base substitution A G intron_variant MELA-AU 12 6959159 6959159 single base substitution A G upstream_gene_variant MELA-AU 12 6959832 6959832 single base substitution G A exon_variant MELA-AU 12 6959832 6959832 single base substitution G A intron_variant MELA-AU 12 6959832 6959832 single base substitution G A upstream_gene_variant MELA-AU 12 6959886 6959886 single base substitution G A exon_variant MELA-AU 12 6959886 6959886 single base substitution G A intron_variant MELA-AU 12 6959886 6959886 single base substitution G A upstream_gene_variant MELA-AU 12 6960283 6960283 single base substitution C T 5_prime_UTR_variant MELA-AU 12 6960283 6960283 single base substitution C T intron_variant MELA-AU 12 6960283 6960283 single base substitution C T upstream_gene_variant MELA-AU 12 6960462 6960462 single base substitution C T 5_prime_UTR_variant MELA-AU 12 6960462 6960462 single base substitution C T upstream_gene_variant MELA-AU 12 6960504 6960504 single base substitution C T 5_prime_UTR_variant MELA-AU 12 6960504 6960504 single base substitution C T upstream_gene_variant MELA-AU 12 6961109 6961109 single base substitution G A 5_prime_UTR_variant MELA-AU 12 6961109 6961109 single base substitution G A upstream_gene_variant MELA-AU 12 6961546 6961546 single base substitution C T upstream_gene_variant MELA-AU 12 6961660 6961660 single base substitution C T upstream_gene_variant MELA-AU 12 6961711 6961711 single base substitution C T upstream_gene_variant MELA-AU 12 6962158 6962158 single base substitution G A upstream_gene_variant MELA-AU 12 6963200 6963200 single base substitution C T upstream_gene_variant MELA-AU 12 6963495 6963495 single base substitution C T upstream_gene_variant MELA-AU 12 6963849 6963850 deletion of <=200bp GA - upstream_gene_variant MELA-AU 12 6964821 6964821 single base substitution C T upstream_gene_variant MELA-AU 12 6964861 6964861 single base substitution C T upstream_gene_variant MELA-AU 12 6964919 6964919 single base substitution A G upstream_gene_variant MELA-AU 12 6965607 6965607 single base substitution C T upstream_gene_variant MELA-AU 12 6965610 6965610 single base substitution C T upstream_gene_variant MELA-AU 12 6965637 6965637 single base substitution C T upstream_gene_variant MELA-AU 12 6965797 6965797 single base substitution C T upstream_gene_variant ORCA-IN 12 6964868 6964868 single base substitution G T upstream_gene_variant OV-AU 12 6949999 6949999 single base substitution T G downstream_gene_variant OV-AU 12 6950527 6950527 single base substitution C A downstream_gene_variant OV-AU 12 6956730 6956730 single base substitution G T downstream_gene_variant OV-AU 12 6956730 6956730 single base substitution G T intron_variant OV-AU 12 6959906 6959906 single base substitution G A exon_variant OV-AU 12 6959906 6959906 single base substitution G A intron_variant OV-AU 12 6959906 6959906 single base substitution G A upstream_gene_variant OV-AU 12 6960623 6960623 single base substitution G T 5_prime_UTR_variant OV-AU 12 6960623 6960623 single base substitution G T upstream_gene_variant OV-AU 12 6961646 6961646 single base substitution C G upstream_gene_variant OV-AU 12 6963887 6963887 single base substitution A C upstream_gene_variant OV-AU 12 6963980 6963980 single base substitution C G upstream_gene_variant PACA-AU 12 6949297 6949297 single base substitution G A downstream_gene_variant PACA-AU 12 6950399 6950399 single base substitution C A downstream_gene_variant PACA-AU 12 6954526 6954526 single base substitution G A 3_prime_UTR_variant PACA-AU 12 6954526 6954526 single base substitution G A downstream_gene_variant PACA-AU 12 6954526 6954526 single base substitution G A exon_variant PACA-AU 12 6954702 6954702 deletion of <=200bp G - 3_prime_UTR_variant PACA-AU 12 6954702 6954702 deletion of <=200bp G - downstream_gene_variant PACA-AU 12 6954702 6954702 deletion of <=200bp G - exon_variant PACA-AU 12 6954705 6954705 single base substitution C T 3_prime_UTR_variant PACA-AU 12 6954705 6954705 single base substitution C T downstream_gene_variant PACA-AU 12 6954705 6954705 single base substitution C T exon_variant PACA-AU 12 6965095 6965095 single base substitution A G upstream_gene_variant PACA-CA 12 6949372 6949372 single base substitution C T downstream_gene_variant PACA-CA 12 6953060 6953060 deletion of <=200bp C - downstream_gene_variant PACA-CA 12 6954034 6954034 single base substitution A G 3_prime_UTR_variant PACA-CA 12 6954034 6954034 single base substitution A G downstream_gene_variant PACA-CA 12 6954034 6954034 single base substitution A G exon_variant PACA-CA 12 6954800 6954800 single base substitution C T 3_prime_UTR_variant PACA-CA 12 6954800 6954800 single base substitution C T downstream_gene_variant PACA-CA 12 6954800 6954800 single base substitution C T exon_variant PACA-CA 12 6956133 6956133 single base substitution C T downstream_gene_variant PACA-CA 12 6956133 6956133 single base substitution C T intron_variant PACA-CA 12 6956619 6956621 deletion of <=200bp GCA - downstream_gene_variant PACA-CA 12 6956619 6956621 deletion of <=200bp GCA - intron_variant PACA-CA 12 6956732 6956732 single base substitution G A downstream_gene_variant PACA-CA 12 6956732 6956732 single base substitution G A intron_variant PAEN-AU 12 6949960 6949960 single base substitution A C downstream_gene_variant PBCA-DE 12 6960627 6960627 single base substitution C T 5_prime_UTR_variant PBCA-DE 12 6960627 6960627 single base substitution C T upstream_gene_variant PRAD-CA 12 6961025 6961025 single base substitution T G 5_prime_UTR_variant PRAD-CA 12 6961025 6961025 single base substitution T G upstream_gene_variant PRAD-UK 12 6960911 6960943 deletion of <=200bp GTCCCTCGACTTTCCGACCGGACAGGTCCCCAG - 5_prime_UTR_variant PRAD-UK 12 6960911 6960943 deletion of <=200bp GTCCCTCGACTTTCCGACCGGACAGGTCCCCAG - upstream_gene_variant PRAD-US 12 6950751 6950751 single base substitution A G downstream_gene_variant PRAD-US 12 6964975 6964975 single base substitution G A upstream_gene_variant RECA-EU 12 6949640 6949640 single base substitution T G downstream_gene_variant RECA-EU 12 6956289 6956289 single base substitution C T downstream_gene_variant RECA-EU 12 6956289 6956289 single base substitution C T intron_variant RECA-EU 12 6962635 6962635 single base substitution G C upstream_gene_variant SKCA-BR 12 6950042 6950042 single base substitution A C downstream_gene_variant SKCA-BR 12 6950143 6950143 single base substitution G A downstream_gene_variant SKCA-BR 12 6965462 6965462 single base substitution C T upstream_gene_variant SKCM-US 12 6950463 6950463 single base substitution G A downstream_gene_variant SKCM-US 12 6952194 6952194 single base substitution G A downstream_gene_variant SKCM-US 12 6952642 6952642 single base substitution C T downstream_gene_variant SKCM-US 12 6953077 6953077 single base substitution G A downstream_gene_variant SKCM-US 12 6953089 6953089 single base substitution G A downstream_gene_variant SKCM-US 12 6953123 6953123 single base substitution C G downstream_gene_variant SKCM-US 12 6954844 6954844 single base substitution C T 3_prime_UTR_variant SKCM-US 12 6954844 6954844 single base substitution C T downstream_gene_variant SKCM-US 12 6954844 6954844 single base substitution C T exon_variant SKCM-US 12 6956008 6956008 single base substitution C T downstream_gene_variant SKCM-US 12 6956008 6956008 single base substitution C T exon_variant SKCM-US 12 6956008 6956008 single base substitution C T missense_variant V202I 604G>A SKCM-US 12 6958754 6958754 single base substitution C T downstream_gene_variant SKCM-US 12 6958754 6958754 single base substitution C T exon_variant SKCM-US 12 6958754 6958754 single base substitution C T synonymous_variant R148R 444G>A SKCM-US 12 6958754 6958754 single base substitution C T synonymous_variant R173R 519G>A SKCM-US 12 6958754 6958754 single base substitution C T upstream_gene_variant SKCM-US 12 6958788 6958788 single base substitution G A downstream_gene_variant SKCM-US 12 6958788 6958788 single base substitution G A exon_variant SKCM-US 12 6958788 6958788 single base substitution G A missense_variant P137L 410C>T SKCM-US 12 6958788 6958788 single base substitution G A missense_variant P162L 485C>T SKCM-US 12 6958788 6958788 single base substitution G A upstream_gene_variant SKCM-US 12 6964919 6964919 single base substitution A G upstream_gene_variant SKCM-US 12 6965272 6965272 single base substitution C T upstream_gene_variant SKCM-US 12 6965611 6965611 single base substitution C T upstream_gene_variant SKCM-US 12 6965958 6965958 single base substitution C T upstream_gene_variant STAD-US 12 6953130 6953130 single base substitution C G downstream_gene_variant STAD-US 12 6954785 6954785 single base substitution G A 3_prime_UTR_variant STAD-US 12 6954785 6954785 single base substitution G A downstream_gene_variant STAD-US 12 6954785 6954785 single base substitution G A exon_variant STAD-US 12 6958314 6958314 single base substitution C A 3_prime_UTR_variant STAD-US 12 6958314 6958314 single base substitution C A downstream_gene_variant STAD-US 12 6958314 6958314 single base substitution C A exon_variant STAD-US 12 6958314 6958314 single base substitution C A intron_variant STAD-US 12 6958314 6958314 single base substitution C A stop_gained G209* 625G>T STAD-US 12 6958314 6958314 single base substitution C A stop_gained G234* 700G>T STAD-US 12 6958314 6958314 single base substitution C A upstream_gene_variant STAD-US 12 6958779 6958779 single base substitution C G downstream_gene_variant STAD-US 12 6958779 6958779 single base substitution C G exon_variant STAD-US 12 6958779 6958779 single base substitution C G missense_variant S140T 419G>C STAD-US 12 6958779 6958779 single base substitution C G missense_variant S165T 494G>C STAD-US 12 6958779 6958779 single base substitution C G upstream_gene_variant STAD-US 12 6964600 6964600 single base substitution G A upstream_gene_variant STAD-US 12 6964649 6964649 single base substitution G A upstream_gene_variant THCA-SA 12 6950035 6950035 single base substitution C T downstream_gene_variant THCA-SA 12 6956018 6956018 single base substitution G A downstream_gene_variant THCA-SA 12 6956018 6956018 single base substitution G A exon_variant THCA-SA 12 6956018 6956018 single base substitution G A synonymous_variant H198H 594C>T THCA-SA 12 6956180 6956180 single base substitution C T downstream_gene_variant THCA-SA 12 6956180 6956180 single base substitution C T intron_variant THCA-US 12 6960070 6960070 single base substitution G A exon_variant THCA-US 12 6960070 6960070 single base substitution G A intron_variant THCA-US 12 6960070 6960070 single base substitution G A missense_variant P16L 47C>T THCA-US 12 6960070 6960070 single base substitution G A upstream_gene_variant THCA-US 12 6964920 6964920 single base substitution A G upstream_gene_variant UCEC-US 12 6952674 6952674 single base substitution C T downstream_gene_variant UCEC-US 12 6952957 6952957 single base substitution G A downstream_gene_variant UCEC-US 12 6952968 6952968 single base substitution G A downstream_gene_variant UCEC-US 12 6954872 6954872 single base substitution G A 3_prime_UTR_variant UCEC-US 12 6954872 6954872 single base substitution G A downstream_gene_variant UCEC-US 12 6954872 6954872 single base substitution G A exon_variant UCEC-US 12 6958492 6958492 single base substitution G A downstream_gene_variant UCEC-US 12 6958492 6958492 single base substitution G A exon_variant UCEC-US 12 6958492 6958492 single base substitution G A intron_variant UCEC-US 12 6958492 6958492 single base substitution G A stop_gained R191* 571C>T UCEC-US 12 6958492 6958492 single base substitution G A stop_gained R216* 646C>T UCEC-US 12 6958492 6958492 single base substitution G A upstream_gene_variant UCEC-US 12 6958584 6958584 single base substitution C T downstream_gene_variant UCEC-US 12 6958584 6958584 single base substitution C T exon_variant UCEC-US 12 6958584 6958584 single base substitution C T intron_variant UCEC-US 12 6958584 6958584 single base substitution C T missense_variant R160H 479G>A UCEC-US 12 6958584 6958584 single base substitution C T missense_variant R185H 554G>A UCEC-US 12 6958584 6958584 single base substitution C T splice_region_variant UCEC-US 12 6958584 6958584 single base substitution C T upstream_gene_variant UCEC-US 12 6958831 6958831 single base substitution G C downstream_gene_variant UCEC-US 12 6958831 6958831 single base substitution G C exon_variant UCEC-US 12 6958831 6958831 single base substitution G C missense_variant Q123E 367C>G UCEC-US 12 6958831 6958831 single base substitution G C missense_variant Q148E 442C>G UCEC-US 12 6958831 6958831 single base substitution G C upstream_gene_variant UCEC-US 12 6959719 6959719 single base substitution T C exon_variant UCEC-US 12 6959719 6959719 single base substitution T C synonymous_variant Q54Q 162A>G UCEC-US 12 6959719 6959719 single base substitution T C upstream_gene_variant UCEC-US 12 6964599 6964599 single base substitution C T upstream_gene_variant UCEC-US 12 6965952 6965952 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand C91 COSM942960 c.646C>T p.R216* Substitution - Nonsense 12:6849328-6849328 - LUAD-S01315 COSM344206 c.298G>A p.E100K Substitution - Missense 12:6849811-6849811 - CSCC-10-T COSM4497748 c.503C>T p.S168F Substitution - Missense 12:6849606-6849606 - ESCC_BICR_024T COSM5440855 c.199C>T p.R67C Substitution - Missense 12:6850518-6850518 - HT55 COSM2099583 c.561A>T p.R187S Substitution - Missense 12:6849413-6849413 - TCGA-AA-3811-01 COSM293727 c.254C>A p.P85H Substitution - Missense 12:6849855-6849855 - TCGA-D1-A17Q-01 COSM942963 c.162A>G p.Q54Q Substitution - coding silent 12:6850555-6850555 - TCGA-27-1838-01 COSM3399031 c.217A>G p.I73V Substitution - Missense 12:6850500-6850500 - HCC153 COSM3704383 c.399G>A p.E133E Substitution - coding silent 12:6849710-6849710 - 61 COSM5739564 c.224G>A p.R75Q Substitution - Missense 12:6850493-6850493 - STC246 COSM5051904 c.792C>T p.P264P Substitution - coding silent 12:6849058-6849058 - HCC153T COSM3704383 c.399G>A p.E133E Substitution - coding silent 12:6849710-6849710 - TCGA-HQ-A2OE-01 COSM1299825 c.279G>A p.L93L Substitution - coding silent 12:6849830-6849830 - C037 COSM5524349 c.471G>A p.Q157Q Substitution - coding silent 12:6849638-6849638 - RK108_C01 COSM1628801 c.798G>A p.V266V Substitution - coding silent 12:6849052-6849052 - 11-P8004 COSM4575694 c.346G>A p.A116T Substitution - Missense 12:6849763-6849763 - sysucc-1878T COSM5766929 c.463G>T p.A155S Substitution - Missense 12:6849646-6849646 - YUGURT COSM5375847 c.118C>T p.Q40* Substitution - Nonsense 12:6850835-6850835 - CSCC-40-T COSM4518730 c.774_775GG>AA p.E259K Substitution - Missense 12:6849075-6849076 - CSCC-49-T COSM4567619 c.791_792CC>TT p.P264L Substitution - Missense 12:6849058-6849059 - TCGA-BR-7851-01 COSM4044478 c.700G>T p.G234* Substitution - Nonsense 12:6849150-6849150 - TCGA-CU-A3KJ-01 COSM1299826 c.234G>A p.M78I Substitution - Missense 12:6850483-6850483 - TCGA-AN-A046-01 COSM3812890 c.544+10C>A p.? Unknown 12:6849555-6849555 - CSCC-16-T COSM4559355 c.801G>C p.E267D Substitution - Missense 12:6849049-6849049 - TCGA-A8-A094-01 COSM431760 c.515C>T p.S172L Substitution - Missense 12:6849594-6849594 - HCC074T COSM5810265 c.504C>T p.S168S Substitution - coding silent 12:6849605-6849605 - TCGA-IR-A3LK-01 COSM4817836 c.279G>C p.L93L Substitution - coding silent 12:6849830-6849830 - S01542 COSM5669538 c.260G>A p.S87N Substitution - Missense 12:6849849-6849849 - TCGA-D3-A1Q1-06 COSM3464536 c.519G>A p.R173R Substitution - coding silent 12:6849590-6849590 - TCGA-CD-8528-01 COSM4044479 c.494G>C p.S165T Substitution - Missense 12:6849615-6849615 - TCGA-AP-A059-01 COSM942960 c.646C>T p.R216* Substitution - Nonsense 12:6849328-6849328 - G6 COSM1191920 c.15G>T p.K5N Substitution - Missense 12:6850938-6850938 - TCGA-AP-A059-01 COSM942961 c.554G>A p.R185H Substitution - Missense 12:6849420-6849420 - TCGA-EE-A3AE-06 COSM3464537 c.485C>T p.P162L Substitution - Missense 12:6849624-6849624 - sysucc-834T COSM5485631 c.518G>T p.R173M Substitution - Missense 12:6849591-6849591 - TCGA-DJ-A2PT-01 COSM3368931 c.47C>T p.P16L Substitution - Missense 12:6850906-6850906 - GC8_T COSM147404 c.472C>T p.P158S Substitution - Missense 12:6849637-6849637 - TCGA-DI-A0WH-01 COSM942962 c.442C>G p.Q148E Substitution - Missense 12:6849667-6849667 - CSCC-27-T COSM4487507 c.319C>T p.P107S Substitution - Missense 12:6849790-6849790 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.524216 12p13 607749

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.W250R c.748T>C 12 6958266 COREAD C G Missense p.E143Q c.427G>C 12 6958846 COREAD C T Missense p.M78I c.234G>A 12 6959647 BLCA G A Missense p.P162L c.485C>T 12 6958788 CM G A Missense p.P16L c.47C>T 12 6960070 THCA G A Missense p.S172L c.515C>T 12 6958758 BRCA G C Missense p.Q148E c.442C>G 12 6958831 UCEC G T Missense p.R67S c.199C>A 12 6959682 STAD G T Missense p.T76K c.227C>A 12 6959654 LUAD T C Missense p.I73V c.217A>G 12 6959664 GBM