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 19 4446075 4446075 + Missense_Mutation SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr19:4446075C>T c.1171G>A c.(1171-1173)Gag>Aag p.E391K BLCA 19 4446144 4446144 + Missense_Mutation SNP C C T TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chr19:4446144C>T c.1102G>A c.(1102-1104)Gag>Aag p.E368K BLCA 19 4446589 4446589 + Silent SNP G G C TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:4446589G>C c.828C>G c.(826-828)gtC>gtG p.V276V BLCA 19 4446708 4446708 + Missense_Mutation SNP C C T TCGA-ZF-A9R2-01A-11D-A391-08 TCGA-ZF-A9R2-10A-01D-A394-08 g.chr19:4446708C>T c.709G>A c.(709-711)Gag>Aag p.E237K BLCA 19 4447594 4447594 + Nonsense_Mutation SNP C C A TCGA-DK-A2I2-01A-11D-A17V-08 TCGA-DK-A2I2-10A-01D-A17V-08 g.chr19:4447594C>A c.568G>T c.(568-570)Gag>Tag p.E190* BLCA 19 4453475 4453475 + Missense_Mutation SNP C C T TCGA-DK-A3X2-01A-11D-A22Z-08 TCGA-DK-A3X2-10A-01D-A22Z-08 g.chr19:4453475C>T c.292G>A c.(292-294)Gag>Aag p.E98K BLCA 19 4453498 4453498 + Missense_Mutation SNP T T G TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr19:4453498T>G c.269A>C c.(268-270)gAa>gCa p.E90A BLCA 19 4453499 4453499 + Missense_Mutation SNP C C T TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr19:4453499C>T c.268G>A c.(268-270)Gaa>Aaa p.E90K BLCA 19 4453979 4453979 + Silent SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr19:4453979C>T c.195G>A c.(193-195)caG>caA p.Q65Q BRCA 19 4445603 4445603 + Silent SNP C C G TCGA-GM-A2D9-01A-11D-A18P-09 TCGA-GM-A2D9-11A-42D-A18P-09 g.chr19:4445603C>G c.1218G>C c.(1216-1218)ctG>ctC p.L406L CESC 19 4454023 4454023 + Missense_Mutation SNP C C T TCGA-EA-A50E-01A-21D-A26G-09 TCGA-EA-A50E-10A-01D-A26G-09 g.chr19:4454023C>T c.151G>A c.(151-153)Gag>Aag p.E51K CESC 19 4457626 4457626 + Silent SNP G G C TCGA-Q1-A5R2-01A-11D-A28B-09 TCGA-Q1-A5R2-10A-01D-A28E-09 g.chr19:4457626G>C c.69C>G c.(67-69)ctC>ctG p.L23L COAD 19 4445552 4445552 + Silent SNP G G T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr19:4445552G>T c.1269C>A c.(1267-1269)gcC>gcA p.A423A COAD 19 4448379 4448379 + Missense_Mutation SNP T T A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr19:4448379T>A c.475A>T c.(475-477)Atg>Ttg p.M159L COAD 19 4452387 4452387 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr19:4452387C>T c.415G>A c.(415-417)Gcc>Acc p.A139T COAD 19 4453935 4453935 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:4453935C>T c.239G>A c.(238-240)cGa>cAa p.R80Q COAD 19 4457678 4457678 + Missense_Mutation SNP T T C TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr19:4457678T>C c.17A>G c.(16-18)cAg>cGg p.Q6R COADREAD 19 4445552 4445552 + Silent SNP G G T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr19:4445552G>T c.1269C>A c.(1267-1269)gcC>gcA p.A423A COADREAD 19 4448379 4448379 + Missense_Mutation SNP T T A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr19:4448379T>A c.475A>T c.(475-477)Atg>Ttg p.M159L COADREAD 19 4452387 4452387 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr19:4452387C>T c.415G>A c.(415-417)Gcc>Acc p.A139T COADREAD 19 4453935 4453935 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr19:4453935C>T c.239G>A c.(238-240)cGa>cAa p.R80Q COADREAD 19 4457678 4457678 + Missense_Mutation SNP T T C TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr19:4457678T>C c.17A>G c.(16-18)cAg>cGg p.Q6R DLBC 19 4446164 4446164 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr19:4446164G>A c.1082C>T c.(1081-1083)gCg>gTg p.A361V ESCA 19 4446060 4446060 + Missense_Mutation SNP T T C TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr19:4446060T>C c.1186A>G c.(1186-1188)Aac>Gac p.N396D ESCA 19 4453480 4453480 + Missense_Mutation SNP C C T TCGA-IG-A4QT-01A-21D-A27G-09 TCGA-IG-A4QT-10A-02D-A27G-09 g.chr19:4453480C>T c.287G>A c.(286-288)aGc>aAc p.S96N GBM 19 4454085 4454085 + Frame_Shift_Del DEL T T - TCGA-14-1450-01B-01D-1845-08 TCGA-14-1450-10B-01D-1845-08 g.chr19:4454085delT c.89delA c.(88-90)aagfs p.K30fs GBMLGG 19 4446151 4446151 + Silent SNP G G A TCGA-S9-A7QY-01A-11D-A34A-08 TCGA-S9-A7QY-10A-01D-A34A-08 g.chr19:4446151G>A c.1095C>T c.(1093-1095)ttC>ttT p.F365F GBMLGG 19 4452490 4452490 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:4452490C>A c.e4-1 GBMLGG 19 4454085 4454085 + Frame_Shift_Del DEL T T - TCGA-14-1450-01B-01D-1845-08 TCGA-14-1450-10B-01D-1845-08 g.chr19:4454085delT c.89delA c.(88-90)aagfs p.K30fs HNSC 19 4445519 4445519 + Silent SNP C C A TCGA-MZ-A7D7-01A-21D-A34J-08 TCGA-MZ-A7D7-10A-01D-A34M-08 g.chr19:4445519C>A c.1302G>T c.(1300-1302)ctG>ctT p.L434L HNSC 19 4446549 4446549 + Missense_Mutation SNP C C A TCGA-DQ-7592-01A-11D-2078-08 TCGA-DQ-7592-10A-01D-2078-08 g.chr19:4446549C>A c.868G>T c.(868-870)Ggg>Tgg p.G290W HNSC 19 4446697 4446697 + Silent SNP G G A TCGA-D6-8568-01A-11D-2394-08 TCGA-D6-8568-10A-01D-2394-08 g.chr19:4446697G>A c.720C>T c.(718-720)taC>taT p.Y240Y HNSC 19 4447568 4447568 + Silent SNP C C T TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr19:4447568C>T c.594G>A c.(592-594)aaG>aaA p.K198K HNSC 19 4452474 4452474 + Missense_Mutation SNP C C T TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr19:4452474C>T c.328G>A c.(328-330)Gag>Aag p.E110K HNSC 19 4454069 4454069 + Missense_Mutation SNP C C A TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr19:4454069C>A c.105G>T c.(103-105)aaG>aaT p.K35N HNSC 19 4454089 4454089 + Splice_Site SNP C C T TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr19:4454089C>T c.85G>A c.(85-87)Gaa>Aaa p.E29K KIPAN 19 4446542 4446542 + Missense_Mutation SNP A A C TCGA-B0-5099-01A-01D-1421-08 TCGA-B0-5099-11A-01D-1421-08 g.chr19:4446542A>C c.875T>G c.(874-876)tTc>tGc p.F292C KIPAN 19 4446696 4446696 + Missense_Mutation SNP C C T TCGA-UZ-A9PK-01A-11D-A382-10 TCGA-UZ-A9PK-10A-01D-A385-10 g.chr19:4446696C>T c.721G>A c.(721-723)Gtg>Atg p.V241M KIRC 19 4446542 4446542 + Missense_Mutation SNP A A C TCGA-B0-5099-01A-01D-1421-08 TCGA-B0-5099-11A-01D-1421-08 g.chr19:4446542A>C c.875T>G c.(874-876)tTc>tGc p.F292C KIRP 19 4446696 4446696 + Missense_Mutation SNP C C T TCGA-UZ-A9PK-01A-11D-A382-10 TCGA-UZ-A9PK-10A-01D-A385-10 g.chr19:4446696C>T c.721G>A c.(721-723)Gtg>Atg p.V241M LGG 19 4446151 4446151 + Silent SNP G G A TCGA-S9-A7QY-01A-11D-A34A-08 TCGA-S9-A7QY-10A-01D-A34A-08 g.chr19:4446151G>A c.1095C>T c.(1093-1095)ttC>ttT p.F365F LGG 19 4452490 4452490 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:4452490C>A c.e4-1 LIHC 19 4448329 4448329 + Silent SNP C C A TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr19:4448329C>A c.525G>T c.(523-525)gtG>gtT p.V175V LIHC 19 4453507 4453507 + Missense_Mutation SNP A A G TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr19:4453507A>G c.260T>C c.(259-261)cTt>cCt p.L87P LUAD 19 4446666 4446666 + Missense_Mutation SNP G G T TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr19:4446666G>T c.751C>A c.(751-753)Cag>Aag p.Q251K LUSC 19 4446553 4446553 + Silent SNP C C A TCGA-22-5472-01A-01D-1632-08 TCGA-22-5472-11A-11D-1632-08 g.chr19:4446553C>A c.864G>T c.(862-864)ctG>ctT p.L288L LUSC 19 4447574 4447574 + Silent SNP C C T TCGA-46-3768-01A-01D-0983-08 TCGA-46-3768-10A-01D-0983-08 g.chr19:4447574C>T c.588G>A c.(586-588)aaG>aaA p.K196K OV 19 4452483 4452483 + Nonsense_Mutation SNP C C A TCGA-61-1914-01A-01W-0639-09 TCGA-61-1914-11A-01W-0640-09 g.chr19:4452483C>A c.319G>T c.(319-321)Gag>Tag p.E107* OV 19 4454023 4454023 + Missense_Mutation SNP C C T TCGA-30-1718-01A-01W-0633-09 TCGA-30-1718-10A-01W-0633-09 g.chr19:4454023C>T c.151G>A c.(151-153)Gag>Aag p.E51K PAAD 19 4454072 4454072 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:4454072C>A c.102G>T c.(100-102)gaG>gaT p.E34D PAAD 19 4454085 4454085 + Frame_Shift_Del DEL T T - TCGA-F2-A44G-01A-11D-A26I-08 TCGA-F2-A44G-10A-01D-A26I-08 g.chr19:4454085delT c.89delA c.(88-90)aagfs p.K30fs PAAD 19 4454085 4454085 + Frame_Shift_Del DEL T T - TCGA-HZ-A49I-01A-12D-A26I-08 TCGA-HZ-A49I-10A-01D-A26I-08 g.chr19:4454085delT c.89delA c.(88-90)aagfs p.K30fs PAAD 19 4457633 4457633 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:4457633T>C c.62A>G c.(61-63)cAg>cGg p.Q21R PCPG 19 4446365 4446365 + Missense_Mutation SNP C C A TCGA-WB-A81T-01A-11D-A35I-08 TCGA-WB-A81T-10A-01D-A35G-08 g.chr19:4446365C>A c.966G>T c.(964-966)atG>atT p.M322I PRAD 19 4454004 4454004 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:4454004G>A c.170C>T c.(169-171)gCt>gTt p.A57V SARC 19 4445565 4445565 + Missense_Mutation SNP T T C TCGA-PC-A5DO-01A-11D-A26G-09 TCGA-PC-A5DO-10A-01D-A26G-09 g.chr19:4445565T>C c.1256A>G c.(1255-1257)aAg>aGg p.K419R SARC 19 4446615 4446615 + Missense_Mutation SNP C C T TCGA-DX-AB32-01A-11D-A417-09 TCGA-DX-AB32-10A-01D-A41A-09 g.chr19:4446615C>T c.802G>A c.(802-804)Gcc>Acc p.A268T SKCM 19 4446513 4446513 + Missense_Mutation SNP G G A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr19:4446513G>A c.904C>T c.(904-906)Cgg>Tgg p.R302W SKCM 19 4447579 4447579 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr19:4447579G>A c.583C>T c.(583-585)Cgg>Tgg p.R195W SKCM 19 4447596 4447596 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr19:4447596G>A c.566C>T c.(565-567)cCc>cTc p.P189L SKCM 19 4453501 4453501 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:4453501G>A c.266C>T c.(265-267)gCc>gTc p.A89V

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 19 4454060 4454060 single base substitution C T 5_prime_UTR_variant BLCA-CN 19 4454060 4454060 single base substitution C T synonymous_variant Q10Q 30G>A BLCA-CN 19 4454060 4454060 single base substitution C T synonymous_variant Q14Q 42G>A BLCA-CN 19 4454060 4454060 single base substitution C T synonymous_variant Q38Q 114G>A BLCA-CN 19 4454060 4454060 single base substitution C T upstream_gene_variant BLCA-US 19 4446589 4446589 single base substitution G C downstream_gene_variant BLCA-US 19 4446589 4446589 single base substitution G C exon_variant BLCA-US 19 4446589 4446589 single base substitution G C missense_variant S10C 29C>G BLCA-US 19 4446589 4446589 single base substitution G C synonymous_variant V205V 615C>G BLCA-US 19 4446589 4446589 single base substitution G C synonymous_variant V223V 669C>G BLCA-US 19 4446589 4446589 single base substitution G C synonymous_variant V276V 828C>G BLCA-US 19 4453979 4453979 single base substitution C T synonymous_variant Q12Q 36G>A BLCA-US 19 4453979 4453979 single base substitution C T synonymous_variant Q37Q 111G>A BLCA-US 19 4453979 4453979 single base substitution C T synonymous_variant Q41Q 123G>A BLCA-US 19 4453979 4453979 single base substitution C T synonymous_variant Q65Q 195G>A BLCA-US 19 4453979 4453979 single base substitution C T upstream_gene_variant BRCA-EU 19 4441337 4441337 single base substitution A G downstream_gene_variant BRCA-EU 19 4441383 4441383 single base substitution G C downstream_gene_variant BRCA-EU 19 4441827 4441827 single base substitution G A downstream_gene_variant BRCA-EU 19 4441851 4441851 single base substitution C T downstream_gene_variant BRCA-EU 19 4441895 4441895 insertion of <=200bp - A downstream_gene_variant BRCA-EU 19 4443405 4443405 single base substitution C A downstream_gene_variant BRCA-EU 19 4446008 4446008 single base substitution G A downstream_gene_variant BRCA-EU 19 4446008 4446008 single base substitution G A exon_variant BRCA-EU 19 4446008 4446008 single base substitution G A intron_variant BRCA-EU 19 4446594 4446594 single base substitution G C downstream_gene_variant BRCA-EU 19 4446594 4446594 single base substitution G C exon_variant BRCA-EU 19 4446594 4446594 single base substitution G C missense_variant R204G 610C>G BRCA-EU 19 4446594 4446594 single base substitution G C missense_variant R222G 664C>G BRCA-EU 19 4446594 4446594 single base substitution G C missense_variant R275G 823C>G BRCA-EU 19 4446594 4446594 single base substitution G C synonymous_variant A8A 24C>G BRCA-EU 19 4446845 4446845 single base substitution C T downstream_gene_variant BRCA-EU 19 4446845 4446845 single base substitution C T exon_variant BRCA-EU 19 4446845 4446845 single base substitution C T missense_variant A159T 475G>A BRCA-EU 19 4446845 4446845 single base substitution C T missense_variant A177T 529G>A BRCA-EU 19 4446845 4446845 single base substitution C T missense_variant A230T 688G>A BRCA-EU 19 4446845 4446845 single base substitution C T upstream_gene_variant BRCA-EU 19 4447838 4447838 single base substitution C G downstream_gene_variant BRCA-EU 19 4447838 4447838 single base substitution C G exon_variant BRCA-EU 19 4447838 4447838 single base substitution C G intron_variant BRCA-EU 19 4447838 4447838 single base substitution C G upstream_gene_variant BRCA-EU 19 4447939 4447939 single base substitution G A downstream_gene_variant BRCA-EU 19 4447939 4447939 single base substitution G A exon_variant BRCA-EU 19 4447939 4447939 single base substitution G A intron_variant BRCA-EU 19 4447939 4447939 single base substitution G A upstream_gene_variant BRCA-EU 19 4447984 4447984 single base substitution C T downstream_gene_variant BRCA-EU 19 4447984 4447984 single base substitution C T exon_variant BRCA-EU 19 4447984 4447984 single base substitution C T intron_variant BRCA-EU 19 4447984 4447984 single base substitution C T upstream_gene_variant BRCA-EU 19 4448741 4448741 single base substitution G A exon_variant BRCA-EU 19 4448741 4448741 single base substitution G A intron_variant BRCA-EU 19 4448741 4448741 single base substitution G A upstream_gene_variant BRCA-EU 19 4450017 4450017 single base substitution G A intron_variant BRCA-EU 19 4450017 4450017 single base substitution G A upstream_gene_variant BRCA-EU 19 4451569 4451569 single base substitution C G intron_variant BRCA-EU 19 4451569 4451569 single base substitution C G upstream_gene_variant BRCA-EU 19 4453287 4453287 single base substitution G A intron_variant BRCA-EU 19 4453287 4453287 single base substitution G A upstream_gene_variant BRCA-EU 19 4458782 4458782 single base substitution G A upstream_gene_variant BRCA-EU 19 4459684 4459684 single base substitution A T upstream_gene_variant BRCA-EU 19 4459754 4459754 single base substitution G A upstream_gene_variant BRCA-EU 19 4459971 4459971 single base substitution A C upstream_gene_variant BRCA-EU 19 4460099 4460099 single base substitution G A upstream_gene_variant BRCA-EU 19 4460139 4460139 single base substitution G A upstream_gene_variant BRCA-EU 19 4460618 4460618 single base substitution C A upstream_gene_variant BRCA-EU 19 4462769 4462769 single base substitution G A upstream_gene_variant BRCA-FR 19 4441337 4441337 single base substitution A G downstream_gene_variant BRCA-FR 19 4450017 4450017 single base substitution G A intron_variant BRCA-FR 19 4450017 4450017 single base substitution G A upstream_gene_variant BRCA-FR 19 4453023 4453023 single base substitution C G intron_variant BRCA-FR 19 4453023 4453023 single base substitution C G upstream_gene_variant BRCA-FR 19 4453287 4453287 single base substitution G A intron_variant BRCA-FR 19 4453287 4453287 single base substitution G A upstream_gene_variant BRCA-FR 19 4455699 4455699 single base substitution C T intron_variant BRCA-FR 19 4455699 4455699 single base substitution C T upstream_gene_variant BRCA-FR 19 4457889 4457889 single base substitution C T upstream_gene_variant BRCA-FR 19 4458782 4458782 single base substitution G A upstream_gene_variant BRCA-FR 19 4460139 4460139 single base substitution G A upstream_gene_variant BRCA-FR 19 4460618 4460618 single base substitution C A upstream_gene_variant BRCA-UK 19 4444628 4444628 single base substitution C T downstream_gene_variant BRCA-UK 19 4452366 4452366 single base substitution G C exon_variant BRCA-UK 19 4452366 4452366 single base substitution G C intron_variant BRCA-UK 19 4452366 4452366 single base substitution G C missense_variant L122V 364C>G BRCA-UK 19 4452366 4452366 single base substitution G C missense_variant L146V 436C>G BRCA-UK 19 4452366 4452366 single base substitution G C missense_variant L93V 277C>G BRCA-UK 19 4452366 4452366 single base substitution G C upstream_gene_variant BRCA-UK 19 4453081 4453081 single base substitution G A intron_variant BRCA-UK 19 4453081 4453081 single base substitution G A upstream_gene_variant BRCA-US 19 4442293 4442293 single base substitution G A downstream_gene_variant BRCA-US 19 4445603 4445603 single base substitution C G downstream_gene_variant BRCA-US 19 4445603 4445603 single base substitution C G exon_variant BRCA-US 19 4445603 4445603 single base substitution C G synonymous_variant L335L 1005G>C BRCA-US 19 4445603 4445603 single base substitution C G synonymous_variant L353L 1059G>C BRCA-US 19 4445603 4445603 single base substitution C G synonymous_variant L406L 1218G>C BRCA-US 19 4445603 4445603 single base substitution C G synonymous_variant L96L 288G>C BTCA-JP 19 4453857 4453869 deletion of <=200bp CCAGGGCCAGGCA - intron_variant BTCA-JP 19 4453857 4453869 deletion of <=200bp CCAGGGCCAGGCA - upstream_gene_variant BTCA-JP 19 4453971 4453971 single base substitution G T missense_variant S15Y 44C>A BTCA-JP 19 4453971 4453971 single base substitution G T missense_variant S40Y 119C>A BTCA-JP 19 4453971 4453971 single base substitution G T missense_variant S44Y 131C>A BTCA-JP 19 4453971 4453971 single base substitution G T missense_variant S68Y 203C>A BTCA-JP 19 4453971 4453971 single base substitution G T upstream_gene_variant CESC-US 19 4454023 4454023 single base substitution C T 5_prime_UTR_variant CESC-US 19 4454023 4454023 single base substitution C T missense_variant E23K 67G>A CESC-US 19 4454023 4454023 single base substitution C T missense_variant E27K 79G>A CESC-US 19 4454023 4454023 single base substitution C T missense_variant E51K 151G>A CESC-US 19 4454023 4454023 single base substitution C T upstream_gene_variant CESC-US 19 4457626 4457626 single base substitution G C synonymous_variant L23L 69C>G CESC-US 19 4457626 4457626 single base substitution G C upstream_gene_variant COAD-US 19 4446363 4446363 single base substitution C T downstream_gene_variant COAD-US 19 4446363 4446363 single base substitution C T exon_variant COAD-US 19 4446363 4446363 single base substitution C T intron_variant COAD-US 19 4446363 4446363 single base substitution C T missense_variant R252Q 755G>A COAD-US 19 4446363 4446363 single base substitution C T missense_variant R270Q 809G>A COAD-US 19 4446363 4446363 single base substitution C T missense_variant R323Q 968G>A COAD-US 19 4446364 4446364 single base substitution G A downstream_gene_variant COAD-US 19 4446364 4446364 single base substitution G A exon_variant COAD-US 19 4446364 4446364 single base substitution G A intron_variant COAD-US 19 4446364 4446364 single base substitution G A missense_variant R252W 754C>T COAD-US 19 4446364 4446364 single base substitution G A missense_variant R270W 808C>T COAD-US 19 4446364 4446364 single base substitution G A missense_variant R323W 967C>T COAD-US 19 4448379 4448379 single base substitution T A downstream_gene_variant COAD-US 19 4448379 4448379 single base substitution T A exon_variant COAD-US 19 4448379 4448379 single base substitution T A missense_variant M106L 316A>T COAD-US 19 4448379 4448379 single base substitution T A missense_variant M159L 475A>T COAD-US 19 4448379 4448379 single base substitution T A missense_variant M88L 262A>T COAD-US 19 4448379 4448379 single base substitution T A upstream_gene_variant COAD-US 19 4457650 4457650 single base substitution C T synonymous_variant K15K 45G>A COAD-US 19 4457650 4457650 single base substitution C T upstream_gene_variant COCA-CN 19 4442328 4442328 single base substitution G A downstream_gene_variant COCA-CN 19 4446365 4446365 single base substitution C T downstream_gene_variant COCA-CN 19 4446365 4446365 single base substitution C T exon_variant COCA-CN 19 4446365 4446365 single base substitution C T intron_variant COCA-CN 19 4446365 4446365 single base substitution C T missense_variant M251I 753G>A COCA-CN 19 4446365 4446365 single base substitution C T missense_variant M269I 807G>A COCA-CN 19 4446365 4446365 single base substitution C T missense_variant M322I 966G>A COCA-CN 19 4446789 4446789 single base substitution C G downstream_gene_variant COCA-CN 19 4446789 4446789 single base substitution C G exon_variant COCA-CN 19 4446789 4446789 single base substitution C G intron_variant COCA-CN 19 4446789 4446789 single base substitution C G upstream_gene_variant COCA-CN 19 4452183 4452183 single base substitution G A intron_variant COCA-CN 19 4452183 4452183 single base substitution G A upstream_gene_variant COCA-CN 19 4452393 4452393 single base substitution G T exon_variant COCA-CN 19 4452393 4452393 single base substitution G T intron_variant COCA-CN 19 4452393 4452393 single base substitution G T synonymous_variant R113R 337C>A COCA-CN 19 4452393 4452393 single base substitution G T synonymous_variant R137R 409C>A COCA-CN 19 4452393 4452393 single base substitution G T synonymous_variant R84R 250C>A COCA-CN 19 4452393 4452393 single base substitution G T upstream_gene_variant COCA-CN 19 4454048 4454048 single base substitution C T 5_prime_UTR_variant COCA-CN 19 4454048 4454048 single base substitution C T synonymous_variant R14R 42G>A COCA-CN 19 4454048 4454048 single base substitution C T synonymous_variant R18R 54G>A COCA-CN 19 4454048 4454048 single base substitution C T synonymous_variant R42R 126G>A COCA-CN 19 4454048 4454048 single base substitution C T upstream_gene_variant ESAD-UK 19 4440137 4440137 single base substitution G C downstream_gene_variant ESAD-UK 19 4440325 4440325 single base substitution C T downstream_gene_variant ESAD-UK 19 4445796 4445796 single base substitution G A downstream_gene_variant ESAD-UK 19 4445796 4445796 single base substitution G A exon_variant ESAD-UK 19 4445796 4445796 single base substitution G A intron_variant ESAD-UK 19 4446444 4446444 single base substitution G A downstream_gene_variant ESAD-UK 19 4446444 4446444 single base substitution G A exon_variant ESAD-UK 19 4446444 4446444 single base substitution G A intron_variant ESAD-UK 19 4446687 4446687 single base substitution C T downstream_gene_variant ESAD-UK 19 4446687 4446687 single base substitution C T exon_variant ESAD-UK 19 4446687 4446687 single base substitution C T missense_variant E173K 517G>A ESAD-UK 19 4446687 4446687 single base substitution C T missense_variant E191K 571G>A ESAD-UK 19 4446687 4446687 single base substitution C T missense_variant E244K 730G>A ESAD-UK 19 4446687 4446687 single base substitution C T upstream_gene_variant ESAD-UK 19 4447408 4447408 single base substitution C T downstream_gene_variant ESAD-UK 19 4447408 4447408 single base substitution C T exon_variant ESAD-UK 19 4447408 4447408 single base substitution C T intron_variant ESAD-UK 19 4447408 4447408 single base substitution C T upstream_gene_variant ESAD-UK 19 4453377 4453377 single base substitution G A intron_variant ESAD-UK 19 4453377 4453377 single base substitution G A upstream_gene_variant ESAD-UK 19 4455239 4455239 single base substitution C T 5_prime_UTR_variant ESAD-UK 19 4455239 4455239 single base substitution C T intron_variant ESAD-UK 19 4455239 4455239 single base substitution C T upstream_gene_variant ESAD-UK 19 4455379 4455379 single base substitution G A intron_variant ESAD-UK 19 4455379 4455379 single base substitution G A upstream_gene_variant ESAD-UK 19 4459639 4459639 single base substitution C T upstream_gene_variant ESAD-UK 19 4461518 4461518 single base substitution C A upstream_gene_variant ESAD-UK 19 4461834 4461834 single base substitution T C upstream_gene_variant GBM-US 19 4454085 4454085 deletion of <=200bp T - 5_prime_UTR_variant GBM-US 19 4454085 4454085 deletion of <=200bp T - frameshift_variant K2 GBM-US 19 4454085 4454085 deletion of <=200bp T - frameshift_variant K30 GBM-US 19 4454085 4454085 deletion of <=200bp T - frameshift_variant K6 GBM-US 19 4454085 4454085 deletion of <=200bp T - upstream_gene_variant KIRC-US 19 4446542 4446542 single base substitution A C downstream_gene_variant KIRC-US 19 4446542 4446542 single base substitution A C exon_variant KIRC-US 19 4446542 4446542 single base substitution A C missense_variant F221C 662T>G KIRC-US 19 4446542 4446542 single base substitution A C missense_variant F239C 716T>G KIRC-US 19 4446542 4446542 single base substitution A C missense_variant F292C 875T>G KIRC-US 19 4446542 4446542 single base substitution A C missense_variant S26A 76T>G LAML-KR 19 4445333 4445333 single base substitution C A 3_prime_UTR_variant LAML-KR 19 4445333 4445333 single base substitution C A downstream_gene_variant LAML-KR 19 4445333 4445333 single base substitution C A exon_variant LICA-FR 19 4446260 4446260 single base substitution C T downstream_gene_variant LICA-FR 19 4446260 4446260 single base substitution C T exon_variant LICA-FR 19 4446260 4446260 single base substitution C T intron_variant LIHC-US 19 4448329 4448329 single base substitution C A downstream_gene_variant LIHC-US 19 4448329 4448329 single base substitution C A exon_variant LIHC-US 19 4448329 4448329 single base substitution C A synonymous_variant V104V 312G>T LIHC-US 19 4448329 4448329 single base substitution C A synonymous_variant V122V 366G>T LIHC-US 19 4448329 4448329 single base substitution C A synonymous_variant V175V 525G>T LIHC-US 19 4448329 4448329 single base substitution C A upstream_gene_variant LINC-JP 19 4446346 4446346 single base substitution G A downstream_gene_variant LINC-JP 19 4446346 4446346 single base substitution G A exon_variant LINC-JP 19 4446346 4446346 single base substitution G A intron_variant LINC-JP 19 4446346 4446346 single base substitution G A missense_variant R258W 772C>T LINC-JP 19 4446346 4446346 single base substitution G A missense_variant R276W 826C>T LINC-JP 19 4446346 4446346 single base substitution G A missense_variant R329W 985C>T LINC-JP 19 4452425 4452425 single base substitution G A intron_variant LINC-JP 19 4452425 4452425 single base substitution G A missense_variant P102L 305C>T LINC-JP 19 4452425 4452425 single base substitution G A missense_variant P126L 377C>T LINC-JP 19 4452425 4452425 single base substitution G A missense_variant P73L 218C>T LINC-JP 19 4452425 4452425 single base substitution G A upstream_gene_variant LINC-JP 19 4453857 4453869 deletion of <=200bp CCAGGGCCAGGCA - intron_variant LINC-JP 19 4453857 4453869 deletion of <=200bp CCAGGGCCAGGCA - upstream_gene_variant LINC-JP 19 4453870 4453870 insertion of <=200bp - T intron_variant LINC-JP 19 4453870 4453870 insertion of <=200bp - T upstream_gene_variant LIRI-JP 19 4440400 4440400 single base substitution G C downstream_gene_variant LIRI-JP 19 4443924 4443924 single base substitution G T downstream_gene_variant LIRI-JP 19 4444827 4444827 single base substitution G A downstream_gene_variant LIRI-JP 19 4447653 4447653 single base substitution C T downstream_gene_variant LIRI-JP 19 4447653 4447653 single base substitution C T exon_variant LIRI-JP 19 4447653 4447653 single base substitution C T intron_variant LIRI-JP 19 4447653 4447653 single base substitution C T upstream_gene_variant LIRI-JP 19 4448638 4448638 single base substitution C T exon_variant LIRI-JP 19 4448638 4448638 single base substitution C T intron_variant LIRI-JP 19 4448638 4448638 single base substitution C T upstream_gene_variant LIRI-JP 19 4450793 4450793 single base substitution C A intron_variant LIRI-JP 19 4450793 4450793 single base substitution C A upstream_gene_variant LIRI-JP 19 4451781 4451781 single base substitution T C intron_variant LIRI-JP 19 4451781 4451781 single base substitution T C upstream_gene_variant LIRI-JP 19 4451827 4451827 single base substitution G T intron_variant LIRI-JP 19 4451827 4451827 single base substitution G T upstream_gene_variant LIRI-JP 19 4452206 4452206 single base substitution G T intron_variant LIRI-JP 19 4452206 4452206 single base substitution G T upstream_gene_variant LIRI-JP 19 4459920 4459920 single base substitution C T upstream_gene_variant LIRI-JP 19 4460744 4460744 single base substitution T G upstream_gene_variant LIRI-JP 19 4462804 4462804 single base substitution T C upstream_gene_variant LUSC-KR 19 4440844 4440844 single base substitution C T downstream_gene_variant LUSC-KR 19 4444647 4444647 single base substitution C A downstream_gene_variant LUSC-KR 19 4446709 4446709 single base substitution G A downstream_gene_variant LUSC-KR 19 4446709 4446709 single base substitution G A exon_variant LUSC-KR 19 4446709 4446709 single base substitution G A synonymous_variant P165P 495C>T LUSC-KR 19 4446709 4446709 single base substitution G A synonymous_variant P183P 549C>T LUSC-KR 19 4446709 4446709 single base substitution G A synonymous_variant P236P 708C>T LUSC-KR 19 4446709 4446709 single base substitution G A upstream_gene_variant LUSC-KR 19 4453325 4453325 single base substitution G C intron_variant LUSC-KR 19 4453325 4453325 single base substitution G C upstream_gene_variant LUSC-KR 19 4455934 4455934 single base substitution G A intron_variant LUSC-KR 19 4455934 4455934 single base substitution G A upstream_gene_variant LUSC-KR 19 4456885 4456885 single base substitution T C intron_variant LUSC-KR 19 4456885 4456885 single base substitution T C upstream_gene_variant LUSC-KR 19 4459885 4459885 single base substitution C A upstream_gene_variant LUSC-KR 19 4462407 4462407 single base substitution G C upstream_gene_variant LUSC-US 19 4446553 4446553 single base substitution C A downstream_gene_variant LUSC-US 19 4446553 4446553 single base substitution C A exon_variant LUSC-US 19 4446553 4446553 single base substitution C A missense_variant C22F 65G>T LUSC-US 19 4446553 4446553 single base substitution C A synonymous_variant L217L 651G>T LUSC-US 19 4446553 4446553 single base substitution C A synonymous_variant L235L 705G>T LUSC-US 19 4446553 4446553 single base substitution C A synonymous_variant L288L 864G>T LUSC-US 19 4447574 4447574 single base substitution C T downstream_gene_variant LUSC-US 19 4447574 4447574 single base substitution C T exon_variant LUSC-US 19 4447574 4447574 single base substitution C T synonymous_variant K125K 375G>A LUSC-US 19 4447574 4447574 single base substitution C T synonymous_variant K143K 429G>A LUSC-US 19 4447574 4447574 single base substitution C T synonymous_variant K196K 588G>A LUSC-US 19 4447574 4447574 single base substitution C T upstream_gene_variant MALY-DE 19 4446995 4446995 single base substitution C T downstream_gene_variant MALY-DE 19 4446995 4446995 single base substitution C T exon_variant MALY-DE 19 4446995 4446995 single base substitution C T intron_variant MALY-DE 19 4446995 4446995 single base substitution C T upstream_gene_variant MALY-DE 19 4448640 4448640 single base substitution C G exon_variant MALY-DE 19 4448640 4448640 single base substitution C G intron_variant MALY-DE 19 4448640 4448640 single base substitution C G upstream_gene_variant MALY-DE 19 4456988 4456988 single base substitution T C intron_variant MALY-DE 19 4456988 4456988 single base substitution T C upstream_gene_variant MELA-AU 19 4440731 4440731 single base substitution C T downstream_gene_variant MELA-AU 19 4440891 4440891 single base substitution C T downstream_gene_variant MELA-AU 19 4442169 4442169 single base substitution C T downstream_gene_variant MELA-AU 19 4442864 4442864 single base substitution C G downstream_gene_variant MELA-AU 19 4442866 4442866 single base substitution C T downstream_gene_variant MELA-AU 19 4442892 4442892 single base substitution G A downstream_gene_variant MELA-AU 19 4443415 4443415 single base substitution C T downstream_gene_variant MELA-AU 19 4443416 4443416 single base substitution G A downstream_gene_variant MELA-AU 19 4443666 4443666 single base substitution C T downstream_gene_variant MELA-AU 19 4444497 4444497 single base substitution G A downstream_gene_variant MELA-AU 19 4446291 4446291 single base substitution C T downstream_gene_variant MELA-AU 19 4446291 4446291 single base substitution C T exon_variant MELA-AU 19 4446291 4446291 single base substitution C T intron_variant MELA-AU 19 4446291 4446291 single base substitution C T missense_variant C276Y 827G>A MELA-AU 19 4446291 4446291 single base substitution C T missense_variant C294Y 881G>A MELA-AU 19 4446291 4446291 single base substitution C T missense_variant C347Y 1040G>A MELA-AU 19 4446551 4446552 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 4446551 4446552 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 19 4446551 4446552 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P218F 652CC>TT MELA-AU 19 4446551 4446552 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P236F 706CC>TT MELA-AU 19 4446551 4446552 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P289F 865CC>TT MELA-AU 19 4446551 4446552 multiple base substitution (>=2bp and <=200bp) GG AA synonymous_variant CL22 MELA-AU 19 4446559 4446559 single base substitution G A downstream_gene_variant MELA-AU 19 4446559 4446559 single base substitution G A exon_variant MELA-AU 19 4446559 4446559 single base substitution G A missense_variant S20L 59C>T MELA-AU 19 4446559 4446559 single base substitution G A synonymous_variant F215F 645C>T MELA-AU 19 4446559 4446559 single base substitution G A synonymous_variant F233F 699C>T MELA-AU 19 4446559 4446559 single base substitution G A synonymous_variant F286F 858C>T MELA-AU 19 4448398 4448398 single base substitution G A exon_variant MELA-AU 19 4448398 4448398 single base substitution G A synonymous_variant D128D 384C>T MELA-AU 19 4448398 4448398 single base substitution G A synonymous_variant D152D 456C>T MELA-AU 19 4448398 4448398 single base substitution G A synonymous_variant D81D 243C>T MELA-AU 19 4448398 4448398 single base substitution G A synonymous_variant D99D 297C>T MELA-AU 19 4448398 4448398 single base substitution G A upstream_gene_variant MELA-AU 19 4448822 4448822 single base substitution G A exon_variant MELA-AU 19 4448822 4448822 single base substitution G A intron_variant MELA-AU 19 4448822 4448822 single base substitution G A upstream_gene_variant MELA-AU 19 4449140 4449140 single base substitution G A exon_variant MELA-AU 19 4449140 4449140 single base substitution G A intron_variant MELA-AU 19 4449140 4449140 single base substitution G A upstream_gene_variant MELA-AU 19 4452261 4452261 single base substitution G A intron_variant MELA-AU 19 4452261 4452261 single base substitution G A upstream_gene_variant MELA-AU 19 4452294 4452294 single base substitution C T intron_variant MELA-AU 19 4452294 4452294 single base substitution C T upstream_gene_variant MELA-AU 19 4453366 4453366 single base substitution C T intron_variant MELA-AU 19 4453366 4453366 single base substitution C T upstream_gene_variant MELA-AU 19 4453387 4453387 single base substitution C T intron_variant MELA-AU 19 4453387 4453387 single base substitution C T upstream_gene_variant MELA-AU 19 4455317 4455318 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 4455317 4455318 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 4455325 4455325 single base substitution C T intron_variant MELA-AU 19 4455325 4455325 single base substitution C T upstream_gene_variant MELA-AU 19 4455754 4455754 single base substitution G A intron_variant MELA-AU 19 4455754 4455754 single base substitution G A upstream_gene_variant MELA-AU 19 4457872 4457872 single base substitution C T upstream_gene_variant MELA-AU 19 4457955 4457955 single base substitution C T upstream_gene_variant MELA-AU 19 4457971 4457971 single base substitution C T upstream_gene_variant MELA-AU 19 4458051 4458051 single base substitution A G upstream_gene_variant MELA-AU 19 4458097 4458097 single base substitution C T upstream_gene_variant MELA-AU 19 4458324 4458324 single base substitution G A upstream_gene_variant MELA-AU 19 4459572 4459572 single base substitution T C upstream_gene_variant MELA-AU 19 4460380 4460380 single base substitution G A upstream_gene_variant MELA-AU 19 4460610 4460610 single base substitution G A upstream_gene_variant MELA-AU 19 4460751 4460751 single base substitution G A upstream_gene_variant MELA-AU 19 4460794 4460794 single base substitution C T upstream_gene_variant MELA-AU 19 4460958 4460958 single base substitution G A upstream_gene_variant MELA-AU 19 4461010 4461010 single base substitution G A upstream_gene_variant MELA-AU 19 4461211 4461211 single base substitution G A upstream_gene_variant MELA-AU 19 4461227 4461227 single base substitution G A upstream_gene_variant MELA-AU 19 4461230 4461230 single base substitution C T upstream_gene_variant MELA-AU 19 4461324 4461324 single base substitution C T upstream_gene_variant MELA-AU 19 4461580 4461580 single base substitution G A upstream_gene_variant MELA-AU 19 4461820 4461821 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 4461947 4461947 single base substitution C T upstream_gene_variant MELA-AU 19 4462248 4462248 single base substitution G A upstream_gene_variant ORCA-IN 19 4441715 4441715 single base substitution A G downstream_gene_variant ORCA-IN 19 4457172 4457172 single base substitution G A intron_variant ORCA-IN 19 4457172 4457172 single base substitution G A upstream_gene_variant OV-AU 19 4457194 4457194 single base substitution C T intron_variant OV-AU 19 4457194 4457194 single base substitution C T upstream_gene_variant OV-AU 19 4458341 4458341 single base substitution G A upstream_gene_variant PACA-AU 19 4452595 4452595 single base substitution C T intron_variant PACA-AU 19 4452595 4452595 single base substitution C T upstream_gene_variant PACA-AU 19 4460754 4460754 single base substitution G A upstream_gene_variant PACA-CA 19 4441552 4441552 single base substitution C T downstream_gene_variant PACA-CA 19 4443220 4443220 single base substitution C T downstream_gene_variant PACA-CA 19 4447643 4447643 single base substitution G A downstream_gene_variant PACA-CA 19 4447643 4447643 single base substitution G A exon_variant PACA-CA 19 4447643 4447643 single base substitution G A intron_variant PACA-CA 19 4447643 4447643 single base substitution G A upstream_gene_variant PACA-CA 19 4447704 4447704 single base substitution C T downstream_gene_variant PACA-CA 19 4447704 4447704 single base substitution C T exon_variant PACA-CA 19 4447704 4447704 single base substitution C T intron_variant PACA-CA 19 4447704 4447704 single base substitution C T upstream_gene_variant PACA-CA 19 4448063 4448063 single base substitution C A downstream_gene_variant PACA-CA 19 4448063 4448063 single base substitution C A exon_variant PACA-CA 19 4448063 4448063 single base substitution C A intron_variant PACA-CA 19 4448063 4448063 single base substitution C A upstream_gene_variant PACA-CA 19 4448377 4448377 single base substitution C T downstream_gene_variant PACA-CA 19 4448377 4448377 single base substitution C T exon_variant PACA-CA 19 4448377 4448377 single base substitution C T missense_variant M106I 318G>A PACA-CA 19 4448377 4448377 single base substitution C T missense_variant M159I 477G>A PACA-CA 19 4448377 4448377 single base substitution C T missense_variant M88I 264G>A PACA-CA 19 4448377 4448377 single base substitution C T upstream_gene_variant PACA-CA 19 4448652 4448652 single base substitution C G exon_variant PACA-CA 19 4448652 4448652 single base substitution C G intron_variant PACA-CA 19 4448652 4448652 single base substitution C G upstream_gene_variant PACA-CA 19 4449083 4449083 single base substitution G A exon_variant PACA-CA 19 4449083 4449083 single base substitution G A intron_variant PACA-CA 19 4449083 4449083 single base substitution G A upstream_gene_variant PACA-CA 19 4449616 4449616 single base substitution G A intron_variant PACA-CA 19 4449616 4449616 single base substitution G A upstream_gene_variant PACA-CA 19 4452388 4452388 single base substitution G A exon_variant PACA-CA 19 4452388 4452388 single base substitution G A intron_variant PACA-CA 19 4452388 4452388 single base substitution G A synonymous_variant D114D 342C>T PACA-CA 19 4452388 4452388 single base substitution G A synonymous_variant D138D 414C>T PACA-CA 19 4452388 4452388 single base substitution G A synonymous_variant D85D 255C>T PACA-CA 19 4452388 4452388 single base substitution G A upstream_gene_variant PACA-CA 19 4452958 4452958 single base substitution C T intron_variant PACA-CA 19 4452958 4452958 single base substitution C T upstream_gene_variant PACA-CA 19 4453619 4453619 single base substitution G A intron_variant PACA-CA 19 4453619 4453619 single base substitution G A upstream_gene_variant PACA-CA 19 4456951 4456951 single base substitution C G intron_variant PACA-CA 19 4456951 4456951 single base substitution C G upstream_gene_variant PACA-CA 19 4459553 4459553 single base substitution G A upstream_gene_variant PACA-CA 19 4459606 4459606 single base substitution G A upstream_gene_variant PACA-CA 19 4462554 4462554 insertion of <=200bp - A upstream_gene_variant PBCA-DE 19 4446013 4446013 single base substitution G A downstream_gene_variant PBCA-DE 19 4446013 4446013 single base substitution G A exon_variant PBCA-DE 19 4446013 4446013 single base substitution G A intron_variant PBCA-DE 19 4446524 4446524 single base substitution T A downstream_gene_variant PBCA-DE 19 4446524 4446524 single base substitution T A exon_variant PBCA-DE 19 4446524 4446524 single base substitution T A missense_variant E227V 680A>T PBCA-DE 19 4446524 4446524 single base substitution T A missense_variant E245V 734A>T PBCA-DE 19 4446524 4446524 single base substitution T A missense_variant E298V 893A>T PBCA-DE 19 4446524 4446524 single base substitution T A missense_variant R32W 94A>T PBCA-DE 19 4457153 4457153 single base substitution T C intron_variant PBCA-DE 19 4457153 4457153 single base substitution T C upstream_gene_variant PBCA-DE 19 4459208 4459208 single base substitution T A upstream_gene_variant PRAD-CA 19 4448121 4448121 single base substitution G T downstream_gene_variant PRAD-CA 19 4448121 4448121 single base substitution G T exon_variant PRAD-CA 19 4448121 4448121 single base substitution G T intron_variant PRAD-CA 19 4448121 4448121 single base substitution G T upstream_gene_variant PRAD-CA 19 4460005 4460005 single base substitution C T upstream_gene_variant PRAD-UK 19 4444610 4444610 single base substitution C T downstream_gene_variant PRAD-UK 19 4448454 4448454 single base substitution G A exon_variant PRAD-UK 19 4448454 4448454 single base substitution G A intron_variant PRAD-UK 19 4448454 4448454 single base substitution G A upstream_gene_variant PRAD-UK 19 4449295 4449295 single base substitution G A exon_variant PRAD-UK 19 4449295 4449295 single base substitution G A intron_variant PRAD-UK 19 4449295 4449295 single base substitution G A upstream_gene_variant PRAD-US 19 4442949 4442949 single base substitution C T downstream_gene_variant READ-US 19 4453935 4453935 single base substitution C T missense_variant R27Q 80G>A READ-US 19 4453935 4453935 single base substitution C T missense_variant R52Q 155G>A READ-US 19 4453935 4453935 single base substitution C T missense_variant R56Q 167G>A READ-US 19 4453935 4453935 single base substitution C T missense_variant R80Q 239G>A READ-US 19 4453935 4453935 single base substitution C T upstream_gene_variant READ-US 19 4454046 4454046 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant READ-US 19 4454046 4454046 single base substitution G A missense_variant P15L 44C>T READ-US 19 4454046 4454046 single base substitution G A missense_variant P19L 56C>T READ-US 19 4454046 4454046 single base substitution G A missense_variant P43L 128C>T READ-US 19 4454046 4454046 single base substitution G A upstream_gene_variant RECA-EU 19 4445734 4445734 single base substitution G T downstream_gene_variant RECA-EU 19 4445734 4445734 single base substitution G T exon_variant RECA-EU 19 4445734 4445734 single base substitution G T intron_variant RECA-EU 19 4452252 4452252 single base substitution G T intron_variant RECA-EU 19 4452252 4452252 single base substitution G T upstream_gene_variant RECA-EU 19 4462742 4462742 single base substitution A G upstream_gene_variant SKCA-BR 19 4440353 4440353 single base substitution C T downstream_gene_variant SKCA-BR 19 4442797 4442797 single base substitution C T downstream_gene_variant SKCA-BR 19 4445073 4445073 single base substitution A G 3_prime_UTR_variant SKCA-BR 19 4445073 4445073 single base substitution A G downstream_gene_variant SKCA-BR 19 4445073 4445073 single base substitution A G exon_variant SKCA-BR 19 4446145 4446145 single base substitution C T downstream_gene_variant SKCA-BR 19 4446145 4446145 single base substitution C T exon_variant SKCA-BR 19 4446145 4446145 single base substitution C T synonymous_variant R296R 888G>A SKCA-BR 19 4446145 4446145 single base substitution C T synonymous_variant R314R 942G>A SKCA-BR 19 4446145 4446145 single base substitution C T synonymous_variant R367R 1101G>A SKCA-BR 19 4446145 4446145 single base substitution C T synonymous_variant R57R 171G>A SKCA-BR 19 4446452 4446452 single base substitution T C downstream_gene_variant SKCA-BR 19 4446452 4446452 single base substitution T C exon_variant SKCA-BR 19 4446452 4446452 single base substitution T C intron_variant SKCA-BR 19 4447294 4447294 single base substitution C A downstream_gene_variant SKCA-BR 19 4447294 4447294 single base substitution C A exon_variant SKCA-BR 19 4447294 4447294 single base substitution C A intron_variant SKCA-BR 19 4447294 4447294 single base substitution C A upstream_gene_variant SKCA-BR 19 4451921 4451921 single base substitution T G intron_variant SKCA-BR 19 4451921 4451921 single base substitution T G upstream_gene_variant SKCA-BR 19 4452668 4452668 single base substitution C T intron_variant SKCA-BR 19 4452668 4452668 single base substitution C T upstream_gene_variant SKCA-BR 19 4454593 4454593 single base substitution C T intron_variant SKCA-BR 19 4454593 4454593 single base substitution C T upstream_gene_variant SKCA-BR 19 4454763 4454763 single base substitution T C intron_variant SKCA-BR 19 4454763 4454763 single base substitution T C upstream_gene_variant SKCA-BR 19 4457650 4457650 single base substitution C T synonymous_variant K15K 45G>A SKCA-BR 19 4457650 4457650 single base substitution C T upstream_gene_variant SKCA-BR 19 4457790 4457791 deletion of <=200bp AT - 5_prime_UTR_variant SKCA-BR 19 4457790 4457791 deletion of <=200bp AT - upstream_gene_variant SKCA-BR 19 4457791 4457794 deletion of <=200bp TTAA - 5_prime_UTR_variant SKCA-BR 19 4457791 4457794 deletion of <=200bp TTAA - upstream_gene_variant SKCA-BR 19 4457796 4457796 single base substitution A T 5_prime_UTR_variant SKCA-BR 19 4457796 4457796 single base substitution A T upstream_gene_variant SKCA-BR 19 4457826 4457826 single base substitution C T upstream_gene_variant SKCA-BR 19 4458172 4458172 single base substitution G A upstream_gene_variant SKCA-BR 19 4458173 4458173 single base substitution G A upstream_gene_variant SKCA-BR 19 4460129 4460129 single base substitution G A upstream_gene_variant SKCA-BR 19 4461485 4461485 single base substitution C T upstream_gene_variant SKCM-US 19 4442295 4442295 single base substitution G A downstream_gene_variant SKCM-US 19 4446513 4446513 single base substitution G A downstream_gene_variant SKCM-US 19 4446513 4446513 single base substitution G A exon_variant SKCM-US 19 4446513 4446513 single base substitution G A missense_variant R231W 691C>T SKCM-US 19 4446513 4446513 single base substitution G A missense_variant R249W 745C>T SKCM-US 19 4446513 4446513 single base substitution G A missense_variant R302W 904C>T SKCM-US 19 4446513 4446513 single base substitution G A synonymous_variant S35S 105C>T SKCM-US 19 4447579 4447579 single base substitution G A downstream_gene_variant SKCM-US 19 4447579 4447579 single base substitution G A exon_variant SKCM-US 19 4447579 4447579 single base substitution G A missense_variant R124W 370C>T SKCM-US 19 4447579 4447579 single base substitution G A missense_variant R142W 424C>T SKCM-US 19 4447579 4447579 single base substitution G A missense_variant R195W 583C>T SKCM-US 19 4447579 4447579 single base substitution G A upstream_gene_variant SKCM-US 19 4447596 4447596 single base substitution G A downstream_gene_variant SKCM-US 19 4447596 4447596 single base substitution G A exon_variant SKCM-US 19 4447596 4447596 single base substitution G A missense_variant P118L 353C>T SKCM-US 19 4447596 4447596 single base substitution G A missense_variant P136L 407C>T SKCM-US 19 4447596 4447596 single base substitution G A missense_variant P189L 566C>T SKCM-US 19 4447596 4447596 single base substitution G A upstream_gene_variant SKCM-US 19 4453501 4453501 single base substitution G A missense_variant A36V 107C>T SKCM-US 19 4453501 4453501 single base substitution G A missense_variant A61V 182C>T SKCM-US 19 4453501 4453501 single base substitution G A missense_variant A65V 194C>T SKCM-US 19 4453501 4453501 single base substitution G A missense_variant A89V 266C>T SKCM-US 19 4453501 4453501 single base substitution G A upstream_gene_variant STAD-US 19 4445546 4445546 single base substitution C T downstream_gene_variant STAD-US 19 4445546 4445546 single base substitution C T exon_variant STAD-US 19 4445546 4445546 single base substitution C T synonymous_variant P115P 345G>A STAD-US 19 4445546 4445546 single base substitution C T synonymous_variant P354P 1062G>A STAD-US 19 4445546 4445546 single base substitution C T synonymous_variant P372P 1116G>A STAD-US 19 4445546 4445546 single base substitution C T synonymous_variant P425P 1275G>A STAD-US 19 4445559 4445559 single base substitution G A downstream_gene_variant STAD-US 19 4445559 4445559 single base substitution G A exon_variant STAD-US 19 4445559 4445559 single base substitution G A missense_variant A111V 332C>T STAD-US 19 4445559 4445559 single base substitution G A missense_variant A350V 1049C>T STAD-US 19 4445559 4445559 single base substitution G A missense_variant A368V 1103C>T STAD-US 19 4445559 4445559 single base substitution G A missense_variant A421V 1262C>T STAD-US 19 4445590 4445590 single base substitution C T downstream_gene_variant STAD-US 19 4445590 4445590 single base substitution C T exon_variant STAD-US 19 4445590 4445590 single base substitution C T missense_variant D101N 301G>A STAD-US 19 4445590 4445590 single base substitution C T missense_variant D340N 1018G>A STAD-US 19 4445590 4445590 single base substitution C T missense_variant D358N 1072G>A STAD-US 19 4445590 4445590 single base substitution C T missense_variant D411N 1231G>A STAD-US 19 4446124 4446124 single base substitution C T downstream_gene_variant STAD-US 19 4446124 4446124 single base substitution C T exon_variant STAD-US 19 4446124 4446124 single base substitution C T stop_gained W303* 909G>A STAD-US 19 4446124 4446124 single base substitution C T stop_gained W321* 963G>A STAD-US 19 4446124 4446124 single base substitution C T stop_gained W374* 1122G>A STAD-US 19 4446124 4446124 single base substitution C T stop_gained W64* 192G>A STAD-US 19 4446179 4446179 single base substitution C T downstream_gene_variant STAD-US 19 4446179 4446179 single base substitution C T exon_variant STAD-US 19 4446179 4446179 single base substitution C T missense_variant R285Q 854G>A STAD-US 19 4446179 4446179 single base substitution C T missense_variant R303Q 908G>A STAD-US 19 4446179 4446179 single base substitution C T missense_variant R356Q 1067G>A STAD-US 19 4446179 4446179 single base substitution C T missense_variant R46Q 137G>A STAD-US 19 4446345 4446345 single base substitution C T downstream_gene_variant STAD-US 19 4446345 4446345 single base substitution C T exon_variant STAD-US 19 4446345 4446345 single base substitution C T intron_variant STAD-US 19 4446345 4446345 single base substitution C T missense_variant R258Q 773G>A STAD-US 19 4446345 4446345 single base substitution C T missense_variant R276Q 827G>A STAD-US 19 4446345 4446345 single base substitution C T missense_variant R329Q 986G>A STAD-US 19 4446367 4446367 single base substitution T C downstream_gene_variant STAD-US 19 4446367 4446367 single base substitution T C exon_variant STAD-US 19 4446367 4446367 single base substitution T C intron_variant STAD-US 19 4446367 4446367 single base substitution T C missense_variant M251V 751A>G STAD-US 19 4446367 4446367 single base substitution T C missense_variant M269V 805A>G STAD-US 19 4446367 4446367 single base substitution T C missense_variant M322V 964A>G STAD-US 19 4446528 4446528 single base substitution C T downstream_gene_variant STAD-US 19 4446528 4446528 single base substitution C T exon_variant STAD-US 19 4446528 4446528 single base substitution C T missense_variant A226T 676G>A STAD-US 19 4446528 4446528 single base substitution C T missense_variant A244T 730G>A STAD-US 19 4446528 4446528 single base substitution C T missense_variant A297T 889G>A STAD-US 19 4446528 4446528 single base substitution C T synonymous_variant Q30Q 90G>A STAD-US 19 4446878 4446878 insertion of <=200bp - A downstream_gene_variant STAD-US 19 4446878 4446878 insertion of <=200bp - A exon_variant STAD-US 19 4446878 4446878 insertion of <=200bp - A frameshift_variant E148V? STAD-US 19 4446878 4446878 insertion of <=200bp - A frameshift_variant E166V? STAD-US 19 4446878 4446878 insertion of <=200bp - A frameshift_variant E219V? STAD-US 19 4446878 4446878 insertion of <=200bp - A upstream_gene_variant STAD-US 19 4446879 4446879 insertion of <=200bp - A downstream_gene_variant STAD-US 19 4446879 4446879 insertion of <=200bp - A exon_variant STAD-US 19 4446879 4446879 insertion of <=200bp - A frameshift_variant F147F? STAD-US 19 4446879 4446879 insertion of <=200bp - A frameshift_variant F165F? STAD-US 19 4446879 4446879 insertion of <=200bp - A frameshift_variant F218F? STAD-US 19 4446879 4446879 insertion of <=200bp - A upstream_gene_variant STAD-US 19 4446914 4446914 single base substitution G A downstream_gene_variant STAD-US 19 4446914 4446914 single base substitution G A exon_variant STAD-US 19 4446914 4446914 single base substitution G A missense_variant R136C 406C>T STAD-US 19 4446914 4446914 single base substitution G A missense_variant R154C 460C>T STAD-US 19 4446914 4446914 single base substitution G A missense_variant R207C 619C>T STAD-US 19 4446914 4446914 single base substitution G A upstream_gene_variant STAD-US 19 4447552 4447552 single base substitution A G downstream_gene_variant STAD-US 19 4447552 4447552 single base substitution A G exon_variant STAD-US 19 4447552 4447552 single base substitution A G missense_variant F133L 397T>C STAD-US 19 4447552 4447552 single base substitution A G missense_variant F151L 451T>C STAD-US 19 4447552 4447552 single base substitution A G missense_variant F204L 610T>C STAD-US 19 4447552 4447552 single base substitution A G upstream_gene_variant STAD-US 19 4453490 4453490 single base substitution C T missense_variant V40I 118G>A STAD-US 19 4453490 4453490 single base substitution C T missense_variant V65I 193G>A STAD-US 19 4453490 4453490 single base substitution C T missense_variant V69I 205G>A STAD-US 19 4453490 4453490 single base substitution C T missense_variant V93I 277G>A STAD-US 19 4453490 4453490 single base substitution C T upstream_gene_variant STAD-US 19 4453928 4453928 single base substitution C A missense_variant Q29H 87G>T STAD-US 19 4453928 4453928 single base substitution C A missense_variant Q54H 162G>T STAD-US 19 4453928 4453928 single base substitution C A missense_variant Q58H 174G>T STAD-US 19 4453928 4453928 single base substitution C A missense_variant Q82H 246G>T STAD-US 19 4453928 4453928 single base substitution C A upstream_gene_variant STAD-US 19 4453937 4453937 single base substitution G A synonymous_variant I26I 78C>T STAD-US 19 4453937 4453937 single base substitution G A synonymous_variant I51I 153C>T STAD-US 19 4453937 4453937 single base substitution G A synonymous_variant I55I 165C>T STAD-US 19 4453937 4453937 single base substitution G A synonymous_variant I79I 237C>T STAD-US 19 4453937 4453937 single base substitution G A upstream_gene_variant THCA-US 19 4446104 4446104 single base substitution G A downstream_gene_variant THCA-US 19 4446104 4446104 single base substitution G A exon_variant THCA-US 19 4446104 4446104 single base substitution G A missense_variant A310V 929C>T THCA-US 19 4446104 4446104 single base substitution G A missense_variant A328V 983C>T THCA-US 19 4446104 4446104 single base substitution G A missense_variant A381V 1142C>T THCA-US 19 4446104 4446104 single base substitution G A missense_variant A71V 212C>T UCEC-US 19 4443092 4443092 single base substitution T A downstream_gene_variant UCEC-US 19 4446053 4446053 single base substitution C T downstream_gene_variant UCEC-US 19 4446053 4446053 single base substitution C T exon_variant UCEC-US 19 4446053 4446053 single base substitution C T missense_variant C327Y 980G>A UCEC-US 19 4446053 4446053 single base substitution C T missense_variant C345Y 1034G>A UCEC-US 19 4446053 4446053 single base substitution C T missense_variant C398Y 1193G>A UCEC-US 19 4446053 4446053 single base substitution C T missense_variant C88Y 263G>A UCEC-US 19 4453935 4453935 single base substitution C T missense_variant R27Q 80G>A UCEC-US 19 4453935 4453935 single base substitution C T missense_variant R52Q 155G>A UCEC-US 19 4453935 4453935 single base substitution C T missense_variant R56Q 167G>A UCEC-US 19 4453935 4453935 single base substitution C T missense_variant R80Q 239G>A UCEC-US 19 4453935 4453935 single base substitution C T upstream_gene_variant UCEC-US 19 4454056 4454056 single base substitution C T 5_prime_UTR_variant UCEC-US 19 4454056 4454056 single base substitution C T missense_variant A12T 34G>A UCEC-US 19 4454056 4454056 single base substitution C T missense_variant A16T 46G>A UCEC-US 19 4454056 4454056 single base substitution C T missense_variant A40T 118G>A UCEC-US 19 4454056 4454056 single base substitution C T upstream_gene_variant UCEC-US 19 4454061 4454061 single base substitution T C 5_prime_UTR_variant UCEC-US 19 4454061 4454061 single base substitution T C missense_variant Q10R 29A>G UCEC-US 19 4454061 4454061 single base substitution T C missense_variant Q14R 41A>G UCEC-US 19 4454061 4454061 single base substitution T C missense_variant Q38R 113A>G UCEC-US 19 4454061 4454061 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 HT55 COSM3289550 c.1135C>G p.L379V Substitution - Missense 19:4446114-4446114 - TCGA-CG-4437-01 COSM4079037 c.986G>A p.R329Q Substitution - Missense 19:4446348-4446348 - H1155 COSM1195303 c.547G>A p.D183N Substitution - Missense 19:4447618-4447618 - TCGA-AP-A0LT-01 COSM997776 c.320A>G p.E107G Substitution - Missense 19:4452485-4452485 - TCGA-GM-A2D9-01 COSM3823332 c.1218G>C p.L406L Substitution - coding silent 19:4445606-4445606 - TCGA-EI-6917-01 COSM286268 c.239G>A p.R80Q Substitution - Missense 19:4453938-4453938 - TCGA-HU-A4H8-01 COSM4079039 c.889G>A p.A297T Substitution - Missense 19:4446531-4446531 - TCGA-D3-A5GU-06 COSM3535388 c.583C>T p.R195W Substitution - Missense 19:4447582-4447582 - TCGA-CG-5733-01 COSM4079034 c.1231G>A p.D411N Substitution - Missense 19:4445593-4445593 - TCGA-61-1914-01 COSM1325277 c.319G>T p.E107* Substitution - Nonsense 19:4452486-4452486 - TCGA-D5-6930-01 COSM3692839 c.967C>T p.R323W Substitution - Missense 19:4446367-4446367 - CSCC-31-T COSM4558213 c.759G>A p.L253L Substitution - coding silent 19:4446661-4446661 - PTC-10C COSM4000778 c.174C>T p.A58A Substitution - coding silent 19:4454003-4454003 - TCGA-G2-A2EO-01 COSM1304725 c.195G>A p.Q65Q Substitution - coding silent 19:4453982-4453982 - I2L-P7-Tumor-Organoid COSM3289554 c.840G>A p.S280S Substitution - coding silent 19:4446580-4446580 - sysucc-1317T COSM5449295 c.409C>A p.R137R Substitution - coding silent 19:4452396-4452396 - SNUH_G16_S1 COSM4000778 c.174C>T p.A58A Substitution - coding silent 19:4454003-4454003 - B100 COSM1750878 c.45G>A p.K15K Substitution - coding silent 19:4457653-4457653 - B14-Tumor COSM3933078 c.114G>A p.Q38Q Substitution - coding silent 19:4454063-4454063 - SNUH_G10_S1 COSM4000778 c.174C>T p.A58A Substitution - coding silent 19:4454003-4454003 - T3090 COSM4738992 c.858C>T p.F286F Substitution - coding silent 19:4446562-4446562 - 36 COSM5733556 c.185G>A p.R62Q Substitution - Missense 19:4453992-4453992 - HCC4T COSM1612368 c.985C>T p.R329W Substitution - Missense 19:4446349-4446349 - TCGA-BR-8487-01 COSM4079035 c.1122G>A p.W374* Substitution - Nonsense 19:4446127-4446127 - CSCC-16-T COSM4522308 c.1155G>C p.Q385H Substitution - Missense 19:4446094-4446094 - TCGA-B7-5816-01 COSM4079045 c.610T>C p.F204L Substitution - Missense 19:4447555-4447555 - Pat_14_B COSM5856072 c.238C>T p.R80* Substitution - Nonsense 19:4453939-4453939 - TCGA-B5-A11E-01 COSM286268 c.239G>A p.R80Q Substitution - Missense 19:4453938-4453938 - TCGA-G4-6298-01 COSM1750878 c.45G>A p.K15K Substitution - coding silent 19:4457653-4457653 - HCC4 COSM1612368 c.985C>T p.R329W Substitution - Missense 19:4446349-4446349 - PCSI_0083_Pa_P_526 COSM3787711 c.414C>T p.D138D Substitution - coding silent 19:4452391-4452391 - LUAD-S01405 COSM398992 c.1044_1045CC>TT p.L348>? Complex 19:4446289-4446290 - TCGA-Q1-A5R2-01 COSM4850554 c.69C>G p.L23L Substitution - coding silent 19:4457629-4457629 - BN24 COSM1612371 c.377C>T p.P126L Substitution - Missense 19:4452428-4452428 - TCGA-EP-A2KA-01 COSM4917353 c.525G>T p.V175V Substitution - coding silent 19:4448332-4448332 - TC71 COSM3289556 c.825C>T p.R275R Substitution - coding silent 19:4446595-4446595 - pfg081T COSM4749024 c.206G>A p.R69Q Substitution - Missense 19:4453971-4453971 - ESCC_114 COSM5639674 c.406C>T p.Q136* Substitution - Nonsense 19:4452399-4452399 - TCGA-AU-3779-01 COSM1393459 c.475A>T p.M159L Substitution - Missense 19:4448382-4448382 - 525 COSM5612202 c.133C>T p.R45C Substitution - Missense 19:4454044-4454044 - TCGA-BR-4362-01 COSM4079060 c.237C>T p.I79I Substitution - coding silent 19:4453940-4453940 - PT09_1 COSM5895062 c.1213C>T p.L405F Substitution - Missense 19:4445611-4445611 - TCGA-DK-A2I4-01 COSM3797202 c.828C>G p.V276V Substitution - coding silent 19:4446592-4446592 - TCGA-CD-A4MG-01 COSM4079038 c.964A>G p.M322V Substitution - Missense 19:4446370-4446370 - HT55 COSM3289549 c.1146G>T p.S382S Substitution - coding silent 19:4446103-4446103 - HX13T COSM1612368 c.985C>T p.R329W Substitution - Missense 19:4446349-4446349 - ML_10_T_01 COSM1750878 c.45G>A p.K15K Substitution - coding silent 19:4457653-4457653 - TCGA-D1-A167-01 COSM997782 c.118G>A p.A40T Substitution - Missense 19:4454059-4454059 - TCGA-HU-A4GN-01 COSM4079036 c.1067G>A p.R356Q Substitution - Missense 19:4446182-4446182 - TCGA-D7-A4YV-01 COSM4079041 c.619C>T p.R207C Substitution - Missense 19:4446917-4446917 - SNU-175 COSM3289741 c.225G>A p.S75S Substitution - coding silent 19:4453952-4453952 - STC263 COSM5056739 c.1293C>T p.P431P Substitution - coding silent 19:4445531-4445531 - BN24T COSM1612371 c.377C>T p.P126L Substitution - Missense 19:4452428-4452428 - TCGA-F1-A448-01 COSM4079033 c.1262C>T p.A421V Substitution - Missense 19:4445562-4445562 - T3225 COSM4738995 c.454G>A p.D152N Substitution - Missense 19:4448403-4448403 - MO_1128 COSM5565281 c.799C>T p.R267C Substitution - Missense 19:4446621-4446621 - T40 COSM5343337 c.942G>A p.L314L Substitution - coding silent 19:4446392-4446392 - PT09_2 COSM5895062 c.1213C>T p.L405F Substitution - Missense 19:4445611-4445611 - LIM2405 COSM4642319 c.1158G>T p.K386N Substitution - Missense 19:4446091-4446091 - ESCC_112 COSM5639476 c.712G>T p.E238* Substitution - Nonsense 19:4446708-4446708 - T55 COSM4738994 c.645C>T p.H215H Substitution - coding silent 19:4446891-4446891 - SJHGG034_D COSM4970632 c.389C>T p.A130V Substitution - Missense 19:4452416-4452416 - T636 COSM4738990 c.1188C>T p.N396N Substitution - coding silent 19:4446061-4446061 - TCGA-22-5472-01 COSM712499 c.864G>T p.L288L Substitution - coding silent 19:4446556-4446556 - REC-1 COSM1740571 c.1240G>A p.V414M Substitution - Missense 19:4445584-4445584 - PTC-73C COSM1750878 c.45G>A p.K15K Substitution - coding silent 19:4457653-4457653 - TCGA-D1-A15X-01 COSM997783 c.113A>G p.Q38R Substitution - Missense 19:4454064-4454064 - EWS502 COSM4581170 c.796G>A p.V266M Substitution - Missense 19:4446624-4446624 - TCGA-AA-A010-01 COSM286268 c.239G>A p.R80Q Substitution - Missense 19:4453938-4453938 - TCGA-EA-A50E-01 COSM1325276 c.151G>A p.E51K Substitution - Missense 19:4454026-4454026 - CCK81 COSM3289548 c.1165G>A p.E389K Substitution - Missense 19:4446084-4446084 - TCGA-DJ-A2Q3-01 COSM3371349 c.1142C>T p.A381V Substitution - Missense 19:4446107-4446107 - TCGA-AY-6197-01 COSM1750878 c.45G>A p.K15K Substitution - coding silent 19:4457653-4457653 - T368 COSM1612368 c.985C>T p.R329W Substitution - Missense 19:4446349-4446349 - YUKLAB COSM1686774 c.442-1G>A p.? Unknown 19:4448416-4448416 - cSCCP7 COSM140186 c.184C>T p.R62W Substitution - Missense 19:4453993-4453993 - TCGA-CD-A4MJ-01 COSM4079056 c.277G>A p.V93I Substitution - Missense 19:4453493-4453493 - CSCC-44-T COSM4495149 c.447C>T p.F149F Substitution - coding silent 19:4448410-4448410 - PCSI_0528_Pa_P_526 COSM5031729 c.477G>A p.M159I Substitution - Missense 19:4448380-4448380 - TCGA-ER-A19P-06 COSM3535378 c.904C>T p.R302W Substitution - Missense 19:4446516-4446516 - T3118 COSM4738996 c.309C>T p.N103N Substitution - coding silent 19:4453461-4453461 - TCGA-FW-A3R5-06 COSM3892797 c.266C>T p.A89V Substitution - Missense 19:4453504-4453504 - ME018T COSM225398 c.558_559CC>GT p.H186>? Complex 19:4447606-4447607 - T3336 COSM4738997 c.89delA p.K30fs*31 Deletion - Frameshift 19:4454088-4454088 - 2293755 COSM4606800 c.806A>T p.K269M Substitution - Missense 19:4446614-4446614 - CSCC-15-T COSM4553267 c.585G>A p.R195R Substitution - coding silent 19:4447580-4447580 - LN18 COSM3289682 c.268G>T p.E90* Substitution - Nonsense 19:4453502-4453502 - TCGA-B0-5099-01 COSM474862 c.875T>G p.F292C Substitution - Missense 19:4446545-4446545 - 73 COSM1612368 c.985C>T p.R329W Substitution - Missense 19:4446349-4446349 - TCGA-AA-3864-01 COSM296059 c.415G>A p.A139T Substitution - Missense 19:4452390-4452390 - S00501 COSM3289663 c.409C>T p.R137W Substitution - Missense 19:4452396-4452396 - TCGA-CM-6172-01 COSM3692838 c.968G>A p.R323Q Substitution - Missense 19:4446366-4446366 - LUAD-S01405 COSM398993 c.923C>T p.S308F Substitution - Missense 19:4446411-4446411 - T3080 COSM4738991 c.952C>T p.R318W Substitution - Missense 19:4446382-4446382 - PD13311a COSM5790253 c.823C>G p.R275G Substitution - Missense 19:4446597-4446597 - P147 COSM1737245 c.721G>A p.V241M Substitution - Missense 19:4446699-4446699 - sysucc-1317T COSM5449294 c.966G>A p.M322I Substitution - Missense 19:4446368-4446368 - TCGA-BR-4201-01 COSM4079059 c.246G>T p.Q82H Substitution - Missense 19:4453931-4453931 - TCGA-G2-A2ES-01 COSM1304724 c.268_269GA>AC p.E90T Substitution - Missense 19:4453501-4453502 - RMS77_ COSM4988488 c.766C>T p.H256Y Substitution - Missense 19:4446654-4446654 - TCGA-46-3768-01 COSM712493 c.588G>A p.K196K Substitution - coding silent 19:4447577-4447577 - ccRCC-56 COSM1659558 c.1200+1G>A p.? Unknown 19:4446048-4446048 - 1N55-VS-1T55 COSM4977083 c.509G>T p.R170L Substitution - Missense 19:4448348-4448348 - HCC2998 COSM3289553 c.859G>A p.E287K Substitution - Missense 19:4446561-4446561 - T613 COSM4738993 c.821G>A p.R274H Substitution - Missense 19:4446599-4446599 - TCGA-HF-7132-01 COSM4079032 c.1275G>A p.P425P Substitution - coding silent 19:4445549-4445549 - YUOMEGA COSM5390023 c.669C>T p.F223F Substitution - coding silent 19:4446867-4446867 - TCGA-GF-A6C9-06 COSM4901152 c.566C>T p.P189L Substitution - Missense 19:4447599-4447599 - ESCC_31 COSM5627853 c.719_720insCT p.V241fs*3 Insertion - Frameshift 19:4446700-4446701 - TCGA-EI-6882-01 COSM3289743 c.128C>T p.P43L Substitution - Missense 19:4454049-4454049 - TCGA-D1-A167-01 COSM997748 c.1193G>A p.C398Y Substitution - Missense 19:4446056-4446056 - TCGA-30-1718-01 COSM1325276 c.151G>A p.E51K Substitution - Missense 19:4454026-4454026 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.435255 19p13 611946 2455259|CGAP|BC008288|C/T|coding|Ala5Ala|168|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.F292C c.875T>G 19 4446542 RCCC A G Missense p.F204L c.610T>C 19 4447552 STAD C A Missense p.G290W c.868G>T 19 4446549 HNSC C A Missense p.K35N c.105G>T 19 4454069 HNSC C A Missense p.Q82H c.246G>T 19 4453928 STAD C T Missense p.D411N c.1231G>A 19 4445590 STAD C T Missense p.R329Q c.986G>A 19 4446345 STAD C T Synonymous p.K196K c.588G>A 19 4447574 LUSC C T Synonymous p.Q65Q c.195G>A 19 4453979 BLCA G A Missense p.A381V c.1142C>T 19 4446104 THCA G A Missense p.R302W c.904C>T 19 4446513 CM GG AC Missense p.H186Q c.558_559delinsGT 19 4447603 CM TC GT Missense p.E90T c.268_269delinsAC 19 4453498 BLCA T - Frameshift p.K30Rfs*31 c.89delA 19 4454085 GBM