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 3 10342968 10342968 + Missense_Mutation SNP C C G TCGA-GV-A3JW-01A-11D-A20D-08 TCGA-GV-A3JW-10A-01D-A20D-08 g.chr3:10342968C>G c.946G>C c.(946-948)Gag>Cag p.E316Q BLCA 3 10342988 10342988 + Missense_Mutation SNP G G A TCGA-KQ-A41P-01A-12D-A339-08 TCGA-KQ-A41P-10F-01D-A339-08 g.chr3:10342988G>A c.926C>T c.(925-927)tCc>tTc p.S309F BLCA 3 10353718 10353718 + Silent SNP C C T TCGA-E7-A85H-01A-11D-A34U-08 TCGA-E7-A85H-10B-01D-A34X-08 g.chr3:10353718C>T c.381G>A c.(379-381)ggG>ggA p.G127G BLCA 3 10354352 10354352 + Missense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr3:10354352G>A c.227C>T c.(226-228)tCg>tTg p.S76L BLCA 3 10354378 10354378 + Silent SNP G G A TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chr3:10354378G>A c.201C>T c.(199-201)caC>caT p.H67H BRCA 3 10343034 10343034 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr3:10343034C>T c.880G>A c.(880-882)Gat>Aat p.D294N BRCA 3 10354287 10354287 + Missense_Mutation SNP C C T TCGA-BH-A0BV-01A-11W-A019-09 TCGA-BH-A0BV-10A-01W-A021-09 g.chr3:10354287C>T c.292G>A c.(292-294)Gag>Aag p.E98K BRCA 3 10354321 10354321 + Nonsense_Mutation SNP C C T TCGA-D8-A140-01A-11D-A10Y-09 TCGA-D8-A140-10A-01D-A110-09 g.chr3:10354321C>T c.258G>A c.(256-258)tgG>tgA p.W86* COAD 3 10342987 10342987 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:10342987G>A c.927C>T c.(925-927)tcC>tcT p.S309S COAD 3 10343028 10343028 + Nonsense_Mutation SNP G G A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr3:10343028G>A c.886C>T c.(886-888)Cag>Tag p.Q296* COAD 3 10345765 10345765 + Missense_Mutation SNP T T C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr3:10345765T>C c.800A>G c.(799-801)cAt>cGt p.H267R COAD 3 10345795 10345795 + Missense_Mutation SNP A A C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:10345795A>C c.770T>G c.(769-771)tTg>tGg p.L257W COAD 3 10346795 10346795 + Silent SNP C C T TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr3:10346795C>T c.630G>A c.(628-630)gcG>gcA p.A210A COAD 3 10357076 10357076 + Silent SNP G G A TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr3:10357076G>A c.93C>T c.(91-93)tgC>tgT p.C31C COADREAD 3 10342987 10342987 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:10342987G>A c.927C>T c.(925-927)tcC>tcT p.S309S COADREAD 3 10343028 10343028 + Nonsense_Mutation SNP G G A TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr3:10343028G>A c.886C>T c.(886-888)Cag>Tag p.Q296* COADREAD 3 10345765 10345765 + Missense_Mutation SNP T T C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr3:10345765T>C c.800A>G c.(799-801)cAt>cGt p.H267R COADREAD 3 10345795 10345795 + Missense_Mutation SNP A A C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr3:10345795A>C c.770T>G c.(769-771)tTg>tGg p.L257W COADREAD 3 10346795 10346795 + Silent SNP C C T TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr3:10346795C>T c.630G>A c.(628-630)gcG>gcA p.A210A COADREAD 3 10357076 10357076 + Silent SNP G G A TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr3:10357076G>A c.93C>T c.(91-93)tgC>tgT p.C31C ESCA 3 10342968 10342968 + Nonsense_Mutation SNP C C A TCGA-2H-A9GJ-01A-11D-A37C-09 TCGA-2H-A9GJ-11A-11D-A37F-09 g.chr3:10342968C>A c.946G>T c.(946-948)Gag>Tag p.E316* ESCA 3 10354308 10354308 + Missense_Mutation SNP C C T TCGA-L5-A4OW-01A-11D-A28B-09 TCGA-L5-A4OW-11A-11D-A28E-09 g.chr3:10354308C>T c.271G>A c.(271-273)Ggc>Agc p.G91S ESCA 3 10357052 10357052 + Silent SNP G G T TCGA-Z6-A9VB-01A-21D-A37C-09 TCGA-Z6-A9VB-10A-01D-A37F-09 g.chr3:10357052G>T c.117C>A c.(115-117)atC>atA p.I39I GBMLGG 3 10353769 10353769 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:10353769G>A c.330C>T c.(328-330)tgC>tgT p.C110C HNSC 3 10357041 10357041 + Missense_Mutation SNP C C T TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr3:10357041C>T c.128G>A c.(127-129)cGc>cAc p.R43H KIPAN 3 10342967 10342967 + Missense_Mutation SNP T T C TCGA-GL-8500-01A-11D-2396-08 TCGA-GL-8500-10A-01D-2396-08 g.chr3:10342967T>C c.947A>G c.(946-948)gAg>gGg p.E316G KIPAN 3 10345822 10345822 + Missense_Mutation SNP G G A TCGA-A3-3331-01A-01W-0886-08 TCGA-A3-3331-11A-01W-0886-08 g.chr3:10345822G>A c.743C>T c.(742-744)gCc>gTc p.A248V KIPAN 3 10346761 10346761 + Missense_Mutation SNP G G A TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr3:10346761G>A c.664C>T c.(664-666)Ccc>Tcc p.P222S KIPAN 3 10346828 10346828 + Silent SNP G G A TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr3:10346828G>A c.597C>T c.(595-597)gaC>gaT p.D199D KIRC 3 10345822 10345822 + Missense_Mutation SNP G G A TCGA-A3-3331-01A-01W-0886-08 TCGA-A3-3331-11A-01W-0886-08 g.chr3:10345822G>A c.743C>T c.(742-744)gCc>gTc p.A248V KIRC 3 10346828 10346828 + Silent SNP G G A TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr3:10346828G>A c.597C>T c.(595-597)gaC>gaT p.D199D KIRP 3 10342967 10342967 + Missense_Mutation SNP T T C TCGA-GL-8500-01A-11D-2396-08 TCGA-GL-8500-10A-01D-2396-08 g.chr3:10342967T>C c.947A>G c.(946-948)gAg>gGg p.E316G KIRP 3 10346761 10346761 + Missense_Mutation SNP G G A TCGA-5P-A9KE-01A-11D-A42J-10 TCGA-5P-A9KE-10A-01D-A42M-10 g.chr3:10346761G>A c.664C>T c.(664-666)Ccc>Tcc p.P222S LGG 3 10353769 10353769 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:10353769G>A c.330C>T c.(328-330)tgC>tgT p.C110C LIHC 3 10347279 10347279 + Missense_Mutation SNP G G A TCGA-DD-A4NV-01A-11D-A30V-10 TCGA-DD-A4NV-10A-01D-A30V-10 g.chr3:10347279G>A c.548C>T c.(547-549)gCa>gTa p.A183V LUAD 3 10346800 10346800 + Missense_Mutation SNP C C G TCGA-55-6982-01A-11D-1945-08 TCGA-55-6982-11A-01D-1945-08 g.chr3:10346800C>G c.625G>C c.(625-627)Gaa>Caa p.E209Q LUAD 3 10354321 10354321 + Missense_Mutation SNP C C G TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr3:10354321C>G c.258G>C c.(256-258)tgG>tgC p.W86C LUAD 3 10354341 10354341 + Missense_Mutation SNP C C G TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr3:10354341C>G c.238G>C c.(238-240)Gac>Cac p.D80H LUSC 3 10343031 10343031 + Missense_Mutation SNP C C G TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr3:10343031C>G c.883G>C c.(883-885)Ggg>Cgg p.G295R LUSC 3 10347307 10347307 + Nonsense_Mutation SNP G G A TCGA-18-3415-01A-01D-0983-08 TCGA-18-3415-11A-01D-0983-08 g.chr3:10347307G>A c.520C>T c.(520-522)Cag>Tag p.Q174* OV 3 10345775 10345775 + Missense_Mutation SNP C C G TCGA-42-2582-01A-01D-1526-09 TCGA-42-2582-10A-01D-1526-09 g.chr3:10345775C>G c.790G>C c.(790-792)Gtg>Ctg p.V264L OV 3 10357041 10357041 + Missense_Mutation SNP C C T TCGA-61-2009-01A-01W-0722-08 TCGA-61-2009-10A-01W-0722-08 g.chr3:10357041C>T c.128G>A c.(127-129)cGc>cAc p.R43H PAAD 3 10342953 10342953 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:10342953C>T c.961G>A c.(961-963)Gag>Aag p.E321K PAAD 3 10354280 10354280 + Missense_Mutation SNP G G A TCGA-HZ-A77P-01A-11D-A33T-08 TCGA-HZ-A77P-10A-01D-A33W-08 g.chr3:10354280G>A c.299C>T c.(298-300)gCg>gTg p.A100V PAAD 3 10354403 10354403 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:10354403G>T c.176C>A c.(175-177)cCt>cAt p.P59H SKCM 3 10346764 10346764 + Missense_Mutation SNP C C T TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr3:10346764C>T c.661G>A c.(661-663)Gcc>Acc p.A221T SKCM 3 10346776 10346776 + Missense_Mutation SNP C C T TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr3:10346776C>T c.649G>A c.(649-651)Gat>Aat p.D217N SKCM 3 10353760 10353760 + Silent SNP G G A TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr3:10353760G>A c.339C>T c.(337-339)ccC>ccT p.P113P SKCM 3 10354368 10354368 + Missense_Mutation SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr3:10354368C>G c.211G>C c.(211-213)Ggc>Cgc p.G71R SKCM 3 10357052 10357052 + Silent SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr3:10357052G>A c.117C>T c.(115-117)atC>atT p.I39I

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 3 10346714 10346714 single base substitution G A intron_variant BLCA-CN 3 10346714 10346714 single base substitution G A splice_region_variant BLCA-CN 3 10357109 10357109 single base substitution C G downstream_gene_variant BLCA-CN 3 10357109 10357109 single base substitution C G exon_variant BLCA-CN 3 10357109 10357109 single base substitution C G missense_variant Q20H 60G>C BLCA-CN 3 10357109 10357109 single base substitution C G missense_variant Q23H 69G>C BLCA-CN 3 10357109 10357109 single base substitution C G missense_variant Q66H 198G>C BLCA-CN 3 10357109 10357109 single base substitution C G missense_variant Q6H 18G>C BLCA-CN 3 10357109 10357109 single base substitution C G upstream_gene_variant BLCA-US 3 10342968 10342968 single base substitution C G downstream_gene_variant BLCA-US 3 10342968 10342968 single base substitution C G exon_variant BLCA-US 3 10342968 10342968 single base substitution C G intron_variant BLCA-US 3 10342968 10342968 single base substitution C G missense_variant E302Q 904G>C BLCA-US 3 10342968 10342968 single base substitution C G missense_variant E316Q 946G>C BLCA-US 3 10342968 10342968 single base substitution C G missense_variant E319Q 955G>C BLCA-US 3 10342968 10342968 single base substitution C G missense_variant E362Q 1084G>C BLCA-US 3 10354378 10354378 single base substitution G A downstream_gene_variant BLCA-US 3 10354378 10354378 single base substitution G A exon_variant BLCA-US 3 10354378 10354378 single base substitution G A synonymous_variant H113H 339C>T BLCA-US 3 10354378 10354378 single base substitution G A synonymous_variant H53H 159C>T BLCA-US 3 10354378 10354378 single base substitution G A synonymous_variant H67H 201C>T BLCA-US 3 10354378 10354378 single base substitution G A synonymous_variant H70H 210C>T BRCA-EU 3 10330820 10330820 single base substitution A T downstream_gene_variant BRCA-EU 3 10332436 10332436 single base substitution C T downstream_gene_variant BRCA-EU 3 10332781 10332781 single base substitution C T downstream_gene_variant BRCA-EU 3 10333613 10333613 single base substitution C G downstream_gene_variant BRCA-EU 3 10334022 10334022 single base substitution C G downstream_gene_variant BRCA-EU 3 10335376 10335376 single base substitution G A intron_variant BRCA-EU 3 10337184 10337184 single base substitution C T intron_variant BRCA-EU 3 10337621 10337621 deletion of <=200bp T - downstream_gene_variant BRCA-EU 3 10337621 10337621 deletion of <=200bp T - intron_variant BRCA-EU 3 10337645 10337645 single base substitution C G downstream_gene_variant BRCA-EU 3 10337645 10337645 single base substitution C G intron_variant BRCA-EU 3 10337873 10337875 deletion of <=200bp TAT - downstream_gene_variant BRCA-EU 3 10337873 10337875 deletion of <=200bp TAT - intron_variant BRCA-EU 3 10337922 10337922 single base substitution T A downstream_gene_variant BRCA-EU 3 10337922 10337922 single base substitution T A intron_variant BRCA-EU 3 10340699 10340699 single base substitution A G downstream_gene_variant BRCA-EU 3 10340699 10340699 single base substitution A G intron_variant BRCA-EU 3 10341543 10341543 single base substitution A T downstream_gene_variant BRCA-EU 3 10341543 10341543 single base substitution A T intron_variant BRCA-EU 3 10343879 10343879 single base substitution G A downstream_gene_variant BRCA-EU 3 10343879 10343879 single base substitution G A intron_variant BRCA-EU 3 10344984 10344984 single base substitution C T downstream_gene_variant BRCA-EU 3 10344984 10344984 single base substitution C T intron_variant BRCA-EU 3 10345458 10345458 single base substitution T C downstream_gene_variant BRCA-EU 3 10345458 10345458 single base substitution T C exon_variant BRCA-EU 3 10345458 10345458 single base substitution T C intron_variant BRCA-EU 3 10346116 10346116 single base substitution T A intron_variant BRCA-EU 3 10348344 10348344 single base substitution G C downstream_gene_variant BRCA-EU 3 10348344 10348344 single base substitution G C intron_variant BRCA-EU 3 10348344 10348344 single base substitution G C upstream_gene_variant BRCA-EU 3 10351044 10351044 single base substitution T G downstream_gene_variant BRCA-EU 3 10351044 10351044 single base substitution T G intron_variant BRCA-EU 3 10351044 10351044 single base substitution T G upstream_gene_variant BRCA-EU 3 10351151 10351151 single base substitution C T downstream_gene_variant BRCA-EU 3 10351151 10351151 single base substitution C T intron_variant BRCA-EU 3 10351151 10351151 single base substitution C T upstream_gene_variant BRCA-EU 3 10355020 10355020 single base substitution C G downstream_gene_variant BRCA-EU 3 10355020 10355020 single base substitution C G exon_variant BRCA-EU 3 10355020 10355020 single base substitution C G intron_variant BRCA-EU 3 10355020 10355020 single base substitution C G upstream_gene_variant BRCA-EU 3 10357608 10357608 single base substitution C G downstream_gene_variant BRCA-EU 3 10357608 10357608 single base substitution C G intron_variant BRCA-EU 3 10357608 10357608 single base substitution C G upstream_gene_variant BRCA-EU 3 10357616 10357616 single base substitution C A downstream_gene_variant BRCA-EU 3 10357616 10357616 single base substitution C A intron_variant BRCA-EU 3 10357616 10357616 single base substitution C A upstream_gene_variant BRCA-EU 3 10357958 10357958 single base substitution C A downstream_gene_variant BRCA-EU 3 10357958 10357958 single base substitution C A intron_variant BRCA-EU 3 10357958 10357958 single base substitution C A upstream_gene_variant BRCA-EU 3 10358047 10358047 single base substitution C T downstream_gene_variant BRCA-EU 3 10358047 10358047 single base substitution C T intron_variant BRCA-EU 3 10358047 10358047 single base substitution C T upstream_gene_variant BRCA-EU 3 10358947 10358947 single base substitution C T downstream_gene_variant BRCA-EU 3 10358947 10358947 single base substitution C T intron_variant BRCA-EU 3 10358947 10358947 single base substitution C T upstream_gene_variant BRCA-EU 3 10359979 10359979 single base substitution A G downstream_gene_variant BRCA-EU 3 10359979 10359979 single base substitution A G intron_variant BRCA-EU 3 10359979 10359979 single base substitution A G upstream_gene_variant BRCA-EU 3 10360927 10360927 single base substitution C G exon_variant BRCA-EU 3 10360927 10360927 single base substitution C G intron_variant BRCA-EU 3 10360927 10360927 single base substitution C G missense_variant E13Q 37G>C BRCA-EU 3 10360927 10360927 single base substitution C G upstream_gene_variant BRCA-EU 3 10361859 10361859 single base substitution C G intron_variant BRCA-EU 3 10361859 10361859 single base substitution C G upstream_gene_variant BRCA-EU 3 10364531 10364531 single base substitution G A upstream_gene_variant BRCA-FR 3 10330329 10330329 single base substitution C T downstream_gene_variant BRCA-FR 3 10332781 10332781 single base substitution C T downstream_gene_variant BRCA-FR 3 10337645 10337645 single base substitution C G downstream_gene_variant BRCA-FR 3 10337645 10337645 single base substitution C G intron_variant BRCA-UK 3 10346764 10346764 single base substitution C T exon_variant BRCA-UK 3 10346764 10346764 single base substitution C T missense_variant A207T 619G>A BRCA-UK 3 10346764 10346764 single base substitution C T missense_variant A221T 661G>A BRCA-UK 3 10346764 10346764 single base substitution C T missense_variant A224T 670G>A BRCA-UK 3 10346764 10346764 single base substitution C T missense_variant A267T 799G>A BRCA-UK 3 10346764 10346764 single base substitution C T upstream_gene_variant BRCA-UK 3 10352770 10352770 single base substitution C T downstream_gene_variant BRCA-UK 3 10352770 10352770 single base substitution C T intron_variant BRCA-UK 3 10357018 10357018 single base substitution C T downstream_gene_variant BRCA-UK 3 10357018 10357018 single base substitution C T exon_variant BRCA-UK 3 10357018 10357018 single base substitution C T missense_variant A37T 109G>A BRCA-UK 3 10357018 10357018 single base substitution C T missense_variant A51T 151G>A BRCA-UK 3 10357018 10357018 single base substitution C T missense_variant A54T 160G>A BRCA-UK 3 10357018 10357018 single base substitution C T missense_variant A97T 289G>A BRCA-UK 3 10357018 10357018 single base substitution C T upstream_gene_variant BRCA-UK 3 10360927 10360927 single base substitution C G exon_variant BRCA-UK 3 10360927 10360927 single base substitution C G intron_variant BRCA-UK 3 10360927 10360927 single base substitution C G missense_variant E13Q 37G>C BRCA-UK 3 10360927 10360927 single base substitution C G upstream_gene_variant BRCA-US 3 10331475 10331475 single base substitution C T downstream_gene_variant BRCA-US 3 10331484 10331484 single base substitution C T downstream_gene_variant BRCA-US 3 10343034 10343034 single base substitution C T downstream_gene_variant BRCA-US 3 10343034 10343034 single base substitution C T exon_variant BRCA-US 3 10343034 10343034 single base substitution C T intron_variant BRCA-US 3 10343034 10343034 single base substitution C T missense_variant D280N 838G>A BRCA-US 3 10343034 10343034 single base substitution C T missense_variant D294N 880G>A BRCA-US 3 10343034 10343034 single base substitution C T missense_variant D297N 889G>A BRCA-US 3 10343034 10343034 single base substitution C T missense_variant D340N 1018G>A BRCA-US 3 10354287 10354287 single base substitution C T downstream_gene_variant BRCA-US 3 10354287 10354287 single base substitution C T exon_variant BRCA-US 3 10354287 10354287 single base substitution C T missense_variant E101K 301G>A BRCA-US 3 10354287 10354287 single base substitution C T missense_variant E144K 430G>A BRCA-US 3 10354287 10354287 single base substitution C T missense_variant E84K 250G>A BRCA-US 3 10354287 10354287 single base substitution C T missense_variant E98K 292G>A BRCA-US 3 10354321 10354321 single base substitution C T downstream_gene_variant BRCA-US 3 10354321 10354321 single base substitution C T exon_variant BRCA-US 3 10354321 10354321 single base substitution C T stop_gained W132* 396G>A BRCA-US 3 10354321 10354321 single base substitution C T stop_gained W72* 216G>A BRCA-US 3 10354321 10354321 single base substitution C T stop_gained W86* 258G>A BRCA-US 3 10354321 10354321 single base substitution C T stop_gained W89* 267G>A BTCA-JP 3 10334306 10334308 deletion of <=200bp AGG - downstream_gene_variant BTCA-JP 3 10343040 10343040 single base substitution A T downstream_gene_variant BTCA-JP 3 10343040 10343040 single base substitution A T exon_variant BTCA-JP 3 10343040 10343040 single base substitution A T intron_variant BTCA-JP 3 10343040 10343040 single base substitution A T missense_variant S278T 832T>A BTCA-JP 3 10343040 10343040 single base substitution A T missense_variant S292T 874T>A BTCA-JP 3 10343040 10343040 single base substitution A T missense_variant S295T 883T>A BTCA-JP 3 10343040 10343040 single base substitution A T missense_variant S338T 1012T>A BTCA-JP 3 10353600 10353600 single base substitution G A downstream_gene_variant BTCA-JP 3 10353600 10353600 single base substitution G A exon_variant BTCA-JP 3 10353600 10353600 single base substitution G A intron_variant BTCA-JP 3 10359869 10359869 insertion of <=200bp - TCAT downstream_gene_variant BTCA-JP 3 10359869 10359869 insertion of <=200bp - TCAT intron_variant BTCA-JP 3 10359869 10359869 insertion of <=200bp - TCAT upstream_gene_variant CLLE-ES 3 10331757 10331757 single base substitution C A downstream_gene_variant CLLE-ES 3 10361557 10361557 single base substitution A G intron_variant CLLE-ES 3 10361557 10361557 single base substitution A G upstream_gene_variant CLLE-ES 3 10362283 10362283 single base substitution C T 5_prime_UTR_variant CLLE-ES 3 10362283 10362283 single base substitution C T intron_variant CLLE-ES 3 10362283 10362283 single base substitution C T upstream_gene_variant CLLE-ES 3 10363421 10363421 deletion of <=200bp T - upstream_gene_variant COAD-US 3 10342987 10342987 single base substitution G A downstream_gene_variant COAD-US 3 10342987 10342987 single base substitution G A exon_variant COAD-US 3 10342987 10342987 single base substitution G A intron_variant COAD-US 3 10342987 10342987 single base substitution G A synonymous_variant S295S 885C>T COAD-US 3 10342987 10342987 single base substitution G A synonymous_variant S309S 927C>T COAD-US 3 10342987 10342987 single base substitution G A synonymous_variant S312S 936C>T COAD-US 3 10342987 10342987 single base substitution G A synonymous_variant S355S 1065C>T COAD-US 3 10346795 10346795 single base substitution C T exon_variant COAD-US 3 10346795 10346795 single base substitution C T synonymous_variant A196A 588G>A COAD-US 3 10346795 10346795 single base substitution C T synonymous_variant A210A 630G>A COAD-US 3 10346795 10346795 single base substitution C T synonymous_variant A213A 639G>A COAD-US 3 10346795 10346795 single base substitution C T synonymous_variant A256A 768G>A COAD-US 3 10346795 10346795 single base substitution C T upstream_gene_variant COCA-CN 3 10345930 10345930 single base substitution T G intron_variant COCA-CN 3 10346828 10346828 single base substitution G A exon_variant COCA-CN 3 10346828 10346828 single base substitution G A synonymous_variant D185D 555C>T COCA-CN 3 10346828 10346828 single base substitution G A synonymous_variant D199D 597C>T COCA-CN 3 10346828 10346828 single base substitution G A synonymous_variant D202D 606C>T COCA-CN 3 10346828 10346828 single base substitution G A synonymous_variant D245D 735C>T COCA-CN 3 10346828 10346828 single base substitution G A upstream_gene_variant COCA-CN 3 10347324 10347324 single base substitution A G exon_variant COCA-CN 3 10347324 10347324 single base substitution A G missense_variant I154T 461T>C COCA-CN 3 10347324 10347324 single base substitution A G missense_variant I168T 503T>C COCA-CN 3 10347324 10347324 single base substitution A G missense_variant I171T 512T>C COCA-CN 3 10347324 10347324 single base substitution A G missense_variant I214T 641T>C COCA-CN 3 10347324 10347324 single base substitution A G upstream_gene_variant COCA-CN 3 10353648 10353648 single base substitution C T downstream_gene_variant COCA-CN 3 10353648 10353648 single base substitution C T exon_variant COCA-CN 3 10353648 10353648 single base substitution C T splice_donor_variant COCA-CN 3 10357041 10357041 single base substitution C T downstream_gene_variant COCA-CN 3 10357041 10357041 single base substitution C T exon_variant COCA-CN 3 10357041 10357041 single base substitution C T missense_variant R29H 86G>A COCA-CN 3 10357041 10357041 single base substitution C T missense_variant R43H 128G>A COCA-CN 3 10357041 10357041 single base substitution C T missense_variant R46H 137G>A COCA-CN 3 10357041 10357041 single base substitution C T missense_variant R89H 266G>A COCA-CN 3 10357041 10357041 single base substitution C T upstream_gene_variant COCA-CN 3 10360721 10360721 single base substitution A C downstream_gene_variant COCA-CN 3 10360721 10360721 single base substitution A C intron_variant COCA-CN 3 10360721 10360721 single base substitution A C upstream_gene_variant COCA-CN 3 10360841 10360841 single base substitution T G 5_prime_UTR_variant COCA-CN 3 10360841 10360841 single base substitution T G downstream_gene_variant COCA-CN 3 10360841 10360841 single base substitution T G exon_variant COCA-CN 3 10360841 10360841 single base substitution T G intron_variant COCA-CN 3 10360841 10360841 single base substitution T G missense_variant K13N 39A>C COCA-CN 3 10360841 10360841 single base substitution T G missense_variant K41N 123A>C COCA-CN 3 10360841 10360841 single base substitution T G upstream_gene_variant COCA-CN 3 10361025 10361025 single base substitution A C intron_variant COCA-CN 3 10361025 10361025 single base substitution A C upstream_gene_variant COCA-CN 3 10362688 10362688 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 3 10362688 10362688 single base substitution G A intron_variant COCA-CN 3 10362688 10362688 single base substitution G A upstream_gene_variant ESAD-UK 3 10333890 10333890 single base substitution C T downstream_gene_variant ESAD-UK 3 10333984 10333984 single base substitution C G downstream_gene_variant ESAD-UK 3 10337424 10337424 single base substitution G C intron_variant ESAD-UK 3 10337447 10337447 single base substitution C A intron_variant ESAD-UK 3 10341084 10341084 single base substitution G A downstream_gene_variant ESAD-UK 3 10341084 10341084 single base substitution G A intron_variant ESAD-UK 3 10341086 10341086 single base substitution C T downstream_gene_variant ESAD-UK 3 10341086 10341086 single base substitution C T intron_variant ESAD-UK 3 10345656 10345656 single base substitution C A downstream_gene_variant ESAD-UK 3 10345656 10345656 single base substitution C A exon_variant ESAD-UK 3 10345656 10345656 single base substitution C A intron_variant ESAD-UK 3 10348153 10348153 single base substitution C G intron_variant ESAD-UK 3 10348153 10348153 single base substitution C G upstream_gene_variant ESAD-UK 3 10351126 10351126 single base substitution C A downstream_gene_variant ESAD-UK 3 10351126 10351126 single base substitution C A intron_variant ESAD-UK 3 10351126 10351126 single base substitution C A upstream_gene_variant ESAD-UK 3 10351810 10351810 single base substitution C T downstream_gene_variant ESAD-UK 3 10351810 10351810 single base substitution C T intron_variant ESAD-UK 3 10351810 10351810 single base substitution C T upstream_gene_variant ESAD-UK 3 10352738 10352738 single base substitution G A downstream_gene_variant ESAD-UK 3 10352738 10352738 single base substitution G A intron_variant ESAD-UK 3 10353080 10353080 single base substitution C T downstream_gene_variant ESAD-UK 3 10353080 10353080 single base substitution C T intron_variant ESAD-UK 3 10353937 10353937 single base substitution A C downstream_gene_variant ESAD-UK 3 10353937 10353937 single base substitution A C intron_variant ESAD-UK 3 10354279 10354279 single base substitution C T downstream_gene_variant ESAD-UK 3 10354279 10354279 single base substitution C T exon_variant ESAD-UK 3 10354279 10354279 single base substitution C T synonymous_variant A100A 300G>A ESAD-UK 3 10354279 10354279 single base substitution C T synonymous_variant A103A 309G>A ESAD-UK 3 10354279 10354279 single base substitution C T synonymous_variant A146A 438G>A ESAD-UK 3 10354279 10354279 single base substitution C T synonymous_variant A86A 258G>A ESAD-UK 3 10354726 10354726 single base substitution C G downstream_gene_variant ESAD-UK 3 10354726 10354726 single base substitution C G exon_variant ESAD-UK 3 10354726 10354726 single base substitution C G intron_variant ESAD-UK 3 10354726 10354726 single base substitution C G upstream_gene_variant ESAD-UK 3 10357118 10357118 single base substitution G A downstream_gene_variant ESAD-UK 3 10357118 10357118 single base substitution G A splice_region_variant ESAD-UK 3 10357118 10357118 single base substitution G A upstream_gene_variant ESAD-UK 3 10359988 10359988 single base substitution C T downstream_gene_variant ESAD-UK 3 10359988 10359988 single base substitution C T intron_variant ESAD-UK 3 10359988 10359988 single base substitution C T upstream_gene_variant ESAD-UK 3 10360622 10360622 single base substitution C T downstream_gene_variant ESAD-UK 3 10360622 10360622 single base substitution C T intron_variant ESAD-UK 3 10360622 10360622 single base substitution C T upstream_gene_variant ESAD-UK 3 10364632 10364632 single base substitution T C upstream_gene_variant ESAD-UK 3 10365963 10365963 deletion of <=200bp C - upstream_gene_variant KIRP-US 3 10342967 10342967 single base substitution T C downstream_gene_variant KIRP-US 3 10342967 10342967 single base substitution T C exon_variant KIRP-US 3 10342967 10342967 single base substitution T C intron_variant KIRP-US 3 10342967 10342967 single base substitution T C missense_variant E302G 905A>G KIRP-US 3 10342967 10342967 single base substitution T C missense_variant E316G 947A>G KIRP-US 3 10342967 10342967 single base substitution T C missense_variant E319G 956A>G KIRP-US 3 10342967 10342967 single base substitution T C missense_variant E362G 1085A>G LICA-FR 3 10345676 10345676 single base substitution T A downstream_gene_variant LICA-FR 3 10345676 10345676 single base substitution T A exon_variant LICA-FR 3 10345676 10345676 single base substitution T A intron_variant LICA-FR 3 10364925 10364925 single base substitution C T upstream_gene_variant LIHC-US 3 10347279 10347279 single base substitution G A exon_variant LIHC-US 3 10347279 10347279 single base substitution G A missense_variant A169V 506C>T LIHC-US 3 10347279 10347279 single base substitution G A missense_variant A183V 548C>T LIHC-US 3 10347279 10347279 single base substitution G A missense_variant A186V 557C>T LIHC-US 3 10347279 10347279 single base substitution G A missense_variant A229V 686C>T LIHC-US 3 10347279 10347279 single base substitution G A upstream_gene_variant LINC-JP 3 10334449 10334449 deletion of <=200bp A - downstream_gene_variant LINC-JP 3 10338894 10338894 single base substitution C A downstream_gene_variant LINC-JP 3 10338894 10338894 single base substitution C A intron_variant LINC-JP 3 10341716 10341716 single base substitution A G downstream_gene_variant LINC-JP 3 10341716 10341716 single base substitution A G intron_variant LINC-JP 3 10342180 10342180 single base substitution C G downstream_gene_variant LINC-JP 3 10342180 10342180 single base substitution C G intron_variant LINC-JP 3 10342571 10342571 single base substitution A C downstream_gene_variant LINC-JP 3 10342571 10342571 single base substitution A C intron_variant LINC-JP 3 10343288 10343288 single base substitution T C downstream_gene_variant LINC-JP 3 10343288 10343288 single base substitution T C intron_variant LINC-JP 3 10347005 10347005 single base substitution C A exon_variant LINC-JP 3 10347005 10347005 single base substitution C A intron_variant LINC-JP 3 10347005 10347005 single base substitution C A upstream_gene_variant LINC-JP 3 10347815 10347815 single base substitution A C intron_variant LINC-JP 3 10347815 10347815 single base substitution A C upstream_gene_variant LINC-JP 3 10350974 10350974 single base substitution T G downstream_gene_variant LINC-JP 3 10350974 10350974 single base substitution T G intron_variant LINC-JP 3 10350974 10350974 single base substitution T G upstream_gene_variant LINC-JP 3 10352616 10352616 single base substitution A C downstream_gene_variant LINC-JP 3 10352616 10352616 single base substitution A C intron_variant LINC-JP 3 10356885 10356885 single base substitution G A downstream_gene_variant LINC-JP 3 10356885 10356885 single base substitution G A exon_variant LINC-JP 3 10356885 10356885 single base substitution G A intron_variant LINC-JP 3 10356885 10356885 single base substitution G A upstream_gene_variant LINC-JP 3 10365707 10365707 single base substitution T G upstream_gene_variant LIRI-JP 3 10336182 10336203 deletion of <=200bp GTACTGAAACTGTTGTCTCAGC - intron_variant LIRI-JP 3 10337672 10337672 single base substitution C A downstream_gene_variant LIRI-JP 3 10337672 10337672 single base substitution C A intron_variant LIRI-JP 3 10338843 10338843 single base substitution T C downstream_gene_variant LIRI-JP 3 10338843 10338843 single base substitution T C intron_variant LIRI-JP 3 10342303 10342303 single base substitution T G downstream_gene_variant LIRI-JP 3 10342303 10342303 single base substitution T G intron_variant LIRI-JP 3 10344574 10344574 single base substitution C A downstream_gene_variant LIRI-JP 3 10344574 10344574 single base substitution C A intron_variant LIRI-JP 3 10346331 10346331 single base substitution T A intron_variant LIRI-JP 3 10348066 10348066 single base substitution T C intron_variant LIRI-JP 3 10348066 10348066 single base substitution T C upstream_gene_variant LIRI-JP 3 10349163 10349163 single base substitution G A downstream_gene_variant LIRI-JP 3 10349163 10349163 single base substitution G A intron_variant LIRI-JP 3 10349163 10349163 single base substitution G A upstream_gene_variant LIRI-JP 3 10349306 10349306 single base substitution T G downstream_gene_variant LIRI-JP 3 10349306 10349306 single base substitution T G intron_variant LIRI-JP 3 10349306 10349306 single base substitution T G upstream_gene_variant LIRI-JP 3 10349720 10349720 single base substitution A G downstream_gene_variant LIRI-JP 3 10349720 10349720 single base substitution A G intron_variant LIRI-JP 3 10349720 10349720 single base substitution A G upstream_gene_variant LIRI-JP 3 10349777 10349777 single base substitution T G downstream_gene_variant LIRI-JP 3 10349777 10349777 single base substitution T G intron_variant LIRI-JP 3 10349777 10349777 single base substitution T G upstream_gene_variant LIRI-JP 3 10349794 10349794 single base substitution T G downstream_gene_variant LIRI-JP 3 10349794 10349794 single base substitution T G intron_variant LIRI-JP 3 10349794 10349794 single base substitution T G upstream_gene_variant LIRI-JP 3 10352958 10352958 single base substitution A C downstream_gene_variant LIRI-JP 3 10352958 10352958 single base substitution A C intron_variant LIRI-JP 3 10354244 10354244 single base substitution G A downstream_gene_variant LIRI-JP 3 10354244 10354244 single base substitution G A intron_variant LIRI-JP 3 10358101 10358101 single base substitution T G downstream_gene_variant LIRI-JP 3 10358101 10358101 single base substitution T G intron_variant LIRI-JP 3 10358101 10358101 single base substitution T G upstream_gene_variant LIRI-JP 3 10360205 10360205 single base substitution G A downstream_gene_variant LIRI-JP 3 10360205 10360205 single base substitution G A intron_variant LIRI-JP 3 10360205 10360205 single base substitution G A upstream_gene_variant LIRI-JP 3 10360437 10360437 single base substitution T C downstream_gene_variant LIRI-JP 3 10360437 10360437 single base substitution T C intron_variant LIRI-JP 3 10360437 10360437 single base substitution T C upstream_gene_variant LIRI-JP 3 10364418 10364418 single base substitution G T upstream_gene_variant LIRI-JP 3 10364505 10364505 single base substitution C T upstream_gene_variant LIRI-JP 3 10366975 10366975 single base substitution A T upstream_gene_variant LUSC-KR 3 10335145 10335145 single base substitution T C intron_variant LUSC-KR 3 10335172 10335172 single base substitution G C intron_variant LUSC-KR 3 10339713 10339713 single base substitution A G downstream_gene_variant LUSC-KR 3 10339713 10339713 single base substitution A G intron_variant LUSC-KR 3 10349855 10349855 single base substitution C G downstream_gene_variant LUSC-KR 3 10349855 10349855 single base substitution C G intron_variant LUSC-KR 3 10349855 10349855 single base substitution C G upstream_gene_variant LUSC-KR 3 10352405 10352405 single base substitution C G downstream_gene_variant LUSC-KR 3 10352405 10352405 single base substitution C G intron_variant LUSC-KR 3 10352405 10352405 single base substitution C G upstream_gene_variant LUSC-KR 3 10354213 10354213 single base substitution T C downstream_gene_variant LUSC-KR 3 10354213 10354213 single base substitution T C intron_variant LUSC-US 3 10331778 10331778 single base substitution G A downstream_gene_variant LUSC-US 3 10343031 10343031 single base substitution C G downstream_gene_variant LUSC-US 3 10343031 10343031 single base substitution C G exon_variant LUSC-US 3 10343031 10343031 single base substitution C G intron_variant LUSC-US 3 10343031 10343031 single base substitution C G missense_variant G281R 841G>C LUSC-US 3 10343031 10343031 single base substitution C G missense_variant G295R 883G>C LUSC-US 3 10343031 10343031 single base substitution C G missense_variant G298R 892G>C LUSC-US 3 10343031 10343031 single base substitution C G missense_variant G341R 1021G>C LUSC-US 3 10347307 10347307 single base substitution G A exon_variant LUSC-US 3 10347307 10347307 single base substitution G A stop_gained Q160* 478C>T LUSC-US 3 10347307 10347307 single base substitution G A stop_gained Q174* 520C>T LUSC-US 3 10347307 10347307 single base substitution G A stop_gained Q177* 529C>T LUSC-US 3 10347307 10347307 single base substitution G A stop_gained Q220* 658C>T LUSC-US 3 10347307 10347307 single base substitution G A upstream_gene_variant MALY-DE 3 10333930 10333930 single base substitution C T downstream_gene_variant MALY-DE 3 10354280 10354280 single base substitution G A downstream_gene_variant MALY-DE 3 10354280 10354280 single base substitution G A exon_variant MALY-DE 3 10354280 10354280 single base substitution G A missense_variant A100V 299C>T MALY-DE 3 10354280 10354280 single base substitution G A missense_variant A103V 308C>T MALY-DE 3 10354280 10354280 single base substitution G A missense_variant A146V 437C>T MALY-DE 3 10354280 10354280 single base substitution G A missense_variant A86V 257C>T MALY-DE 3 10356947 10356947 single base substitution C T downstream_gene_variant MALY-DE 3 10356947 10356947 single base substitution C T exon_variant MALY-DE 3 10356947 10356947 single base substitution C T intron_variant MALY-DE 3 10356947 10356947 single base substitution C T upstream_gene_variant MALY-DE 3 10358679 10358679 single base substitution C T downstream_gene_variant MALY-DE 3 10358679 10358679 single base substitution C T intron_variant MALY-DE 3 10358679 10358679 single base substitution C T upstream_gene_variant MALY-DE 3 10364874 10364874 single base substitution T C upstream_gene_variant MELA-AU 3 10330469 10330469 single base substitution C T downstream_gene_variant MELA-AU 3 10330750 10330750 single base substitution C T downstream_gene_variant MELA-AU 3 10330886 10330886 single base substitution C T downstream_gene_variant MELA-AU 3 10331519 10331519 single base substitution C T downstream_gene_variant MELA-AU 3 10331632 10331632 single base substitution C T downstream_gene_variant MELA-AU 3 10331998 10331998 single base substitution G T downstream_gene_variant MELA-AU 3 10332760 10332760 single base substitution C T downstream_gene_variant MELA-AU 3 10333573 10333573 single base substitution C T downstream_gene_variant MELA-AU 3 10333688 10333688 deletion of <=200bp T - downstream_gene_variant MELA-AU 3 10333840 10333841 multiple base substitution (>=2bp and <=200bp) TC AT downstream_gene_variant MELA-AU 3 10333850 10333850 single base substitution C T downstream_gene_variant MELA-AU 3 10334022 10334022 single base substitution C T downstream_gene_variant MELA-AU 3 10334033 10334033 single base substitution G A downstream_gene_variant MELA-AU 3 10334906 10334906 single base substitution C T exon_variant MELA-AU 3 10335216 10335217 multiple base substitution (>=2bp and <=200bp) AG TT intron_variant MELA-AU 3 10335376 10335376 single base substitution G A intron_variant MELA-AU 3 10335621 10335621 single base substitution C T intron_variant MELA-AU 3 10335914 10335914 single base substitution C T intron_variant MELA-AU 3 10336115 10336115 single base substitution C T intron_variant MELA-AU 3 10337538 10337538 single base substitution C T intron_variant MELA-AU 3 10341584 10341584 single base substitution G A downstream_gene_variant MELA-AU 3 10341584 10341584 single base substitution G A intron_variant MELA-AU 3 10344841 10344841 single base substitution A G downstream_gene_variant MELA-AU 3 10344841 10344841 single base substitution A G intron_variant MELA-AU 3 10344999 10344999 single base substitution C G downstream_gene_variant MELA-AU 3 10344999 10344999 single base substitution C G intron_variant MELA-AU 3 10345644 10345644 single base substitution C T downstream_gene_variant MELA-AU 3 10345644 10345644 single base substitution C T exon_variant MELA-AU 3 10345644 10345644 single base substitution C T intron_variant MELA-AU 3 10345987 10345988 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 10347540 10347541 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 3 10347540 10347541 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 10347540 10347541 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 3 10348955 10348955 single base substitution C T downstream_gene_variant MELA-AU 3 10348955 10348955 single base substitution C T intron_variant MELA-AU 3 10348955 10348955 single base substitution C T upstream_gene_variant MELA-AU 3 10349359 10349359 single base substitution G A downstream_gene_variant MELA-AU 3 10349359 10349359 single base substitution G A intron_variant MELA-AU 3 10349359 10349359 single base substitution G A upstream_gene_variant MELA-AU 3 10349899 10349899 single base substitution G A downstream_gene_variant MELA-AU 3 10349899 10349899 single base substitution G A intron_variant MELA-AU 3 10349899 10349899 single base substitution G A upstream_gene_variant MELA-AU 3 10351548 10351549 multiple base substitution (>=2bp and <=200bp) GT AA downstream_gene_variant MELA-AU 3 10351548 10351549 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 3 10351548 10351549 multiple base substitution (>=2bp and <=200bp) GT AA upstream_gene_variant MELA-AU 3 10352495 10352495 single base substitution A T downstream_gene_variant MELA-AU 3 10352495 10352495 single base substitution A T intron_variant MELA-AU 3 10352495 10352495 single base substitution A T upstream_gene_variant MELA-AU 3 10352817 10352817 single base substitution A G downstream_gene_variant MELA-AU 3 10352817 10352817 single base substitution A G intron_variant MELA-AU 3 10353249 10353249 single base substitution G A downstream_gene_variant MELA-AU 3 10353249 10353249 single base substitution G A intron_variant MELA-AU 3 10353479 10353479 single base substitution T C downstream_gene_variant MELA-AU 3 10353479 10353479 single base substitution T C exon_variant MELA-AU 3 10353479 10353479 single base substitution T C intron_variant MELA-AU 3 10353942 10353942 single base substitution C T downstream_gene_variant MELA-AU 3 10353942 10353942 single base substitution C T intron_variant MELA-AU 3 10355183 10355183 single base substitution G A downstream_gene_variant MELA-AU 3 10355183 10355183 single base substitution G A exon_variant MELA-AU 3 10355183 10355183 single base substitution G A intron_variant MELA-AU 3 10355183 10355183 single base substitution G A upstream_gene_variant MELA-AU 3 10355445 10355445 single base substitution A G downstream_gene_variant MELA-AU 3 10355445 10355445 single base substitution A G exon_variant MELA-AU 3 10355445 10355445 single base substitution A G intron_variant MELA-AU 3 10355445 10355445 single base substitution A G upstream_gene_variant MELA-AU 3 10355730 10355730 single base substitution C A downstream_gene_variant MELA-AU 3 10355730 10355730 single base substitution C A intron_variant MELA-AU 3 10355730 10355730 single base substitution C A upstream_gene_variant MELA-AU 3 10356574 10356574 single base substitution G A downstream_gene_variant MELA-AU 3 10356574 10356574 single base substitution G A intron_variant MELA-AU 3 10356574 10356574 single base substitution G A upstream_gene_variant MELA-AU 3 10358483 10358483 single base substitution C T downstream_gene_variant MELA-AU 3 10358483 10358483 single base substitution C T intron_variant MELA-AU 3 10358483 10358483 single base substitution C T upstream_gene_variant MELA-AU 3 10359829 10359829 single base substitution A G downstream_gene_variant MELA-AU 3 10359829 10359829 single base substitution A G intron_variant MELA-AU 3 10359829 10359829 single base substitution A G upstream_gene_variant MELA-AU 3 10360165 10360165 single base substitution G A downstream_gene_variant MELA-AU 3 10360165 10360165 single base substitution G A intron_variant MELA-AU 3 10360165 10360165 single base substitution G A upstream_gene_variant MELA-AU 3 10360641 10360641 single base substitution C T downstream_gene_variant MELA-AU 3 10360641 10360641 single base substitution C T intron_variant MELA-AU 3 10360641 10360641 single base substitution C T upstream_gene_variant MELA-AU 3 10361016 10361016 single base substitution A G intron_variant MELA-AU 3 10361016 10361016 single base substitution A G upstream_gene_variant MELA-AU 3 10361081 10361081 single base substitution G A intron_variant MELA-AU 3 10361081 10361081 single base substitution G A upstream_gene_variant MELA-AU 3 10362485 10362485 single base substitution A C 5_prime_UTR_variant MELA-AU 3 10362485 10362485 single base substitution A C intron_variant MELA-AU 3 10362485 10362485 single base substitution A C upstream_gene_variant MELA-AU 3 10362746 10362746 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 3 10362746 10362746 single base substitution G A exon_variant MELA-AU 3 10362746 10362746 single base substitution G A upstream_gene_variant MELA-AU 3 10362908 10362908 single base substitution C T upstream_gene_variant MELA-AU 3 10362943 10362943 single base substitution G A upstream_gene_variant MELA-AU 3 10363336 10363336 single base substitution C T upstream_gene_variant MELA-AU 3 10363574 10363574 single base substitution G A upstream_gene_variant MELA-AU 3 10363678 10363678 single base substitution G A upstream_gene_variant MELA-AU 3 10363682 10363682 single base substitution C T upstream_gene_variant MELA-AU 3 10363913 10363913 single base substitution C T upstream_gene_variant MELA-AU 3 10363959 10363959 single base substitution C T upstream_gene_variant MELA-AU 3 10364281 10364281 single base substitution C G upstream_gene_variant MELA-AU 3 10364347 10364347 single base substitution C T upstream_gene_variant MELA-AU 3 10364351 10364351 single base substitution G A upstream_gene_variant MELA-AU 3 10365057 10365057 single base substitution A G upstream_gene_variant MELA-AU 3 10365202 10365202 single base substitution G A upstream_gene_variant MELA-AU 3 10365611 10365612 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 3 10365631 10365631 single base substitution C T upstream_gene_variant MELA-AU 3 10365633 10365633 single base substitution C T upstream_gene_variant MELA-AU 3 10365729 10365729 single base substitution T C upstream_gene_variant MELA-AU 3 10365863 10365863 single base substitution C T upstream_gene_variant MELA-AU 3 10365887 10365887 single base substitution G A upstream_gene_variant MELA-AU 3 10366014 10366014 single base substitution G A upstream_gene_variant MELA-AU 3 10366274 10366274 single base substitution G A upstream_gene_variant MELA-AU 3 10366605 10366605 single base substitution C T upstream_gene_variant MELA-AU 3 10366792 10366792 single base substitution C T upstream_gene_variant MELA-AU 3 10366945 10366945 single base substitution G A upstream_gene_variant MELA-AU 3 10367168 10367168 single base substitution G A upstream_gene_variant MELA-AU 3 10367570 10367570 single base substitution A G upstream_gene_variant MELA-AU 3 10367586 10367586 single base substitution G A upstream_gene_variant ORCA-IN 3 10330918 10330918 single base substitution C G downstream_gene_variant ORCA-IN 3 10337176 10337176 single base substitution C T intron_variant ORCA-IN 3 10359986 10359986 single base substitution C T downstream_gene_variant ORCA-IN 3 10359986 10359986 single base substitution C T intron_variant ORCA-IN 3 10359986 10359986 single base substitution C T upstream_gene_variant ORCA-IN 3 10363425 10363426 multiple base substitution (>=2bp and <=200bp) TA AT upstream_gene_variant OV-AU 3 10331323 10331323 single base substitution G C downstream_gene_variant OV-AU 3 10331463 10331463 single base substitution C G downstream_gene_variant OV-AU 3 10337577 10337577 single base substitution C A intron_variant OV-AU 3 10341628 10341628 single base substitution A G downstream_gene_variant OV-AU 3 10341628 10341628 single base substitution A G intron_variant OV-AU 3 10343946 10343946 single base substitution C T downstream_gene_variant OV-AU 3 10343946 10343946 single base substitution C T intron_variant OV-AU 3 10345426 10345426 single base substitution G C downstream_gene_variant OV-AU 3 10345426 10345426 single base substitution G C exon_variant OV-AU 3 10345426 10345426 single base substitution G C intron_variant OV-AU 3 10354505 10354505 single base substitution C T downstream_gene_variant OV-AU 3 10354505 10354505 single base substitution C T exon_variant OV-AU 3 10354505 10354505 single base substitution C T intron_variant OV-AU 3 10363298 10363298 single base substitution T G upstream_gene_variant OV-AU 3 10363799 10363799 single base substitution C G upstream_gene_variant OV-AU 3 10364534 10364534 single base substitution C G upstream_gene_variant PACA-AU 3 10331597 10331597 single base substitution G A downstream_gene_variant PACA-AU 3 10332606 10332606 single base substitution C T downstream_gene_variant PACA-AU 3 10339023 10339023 single base substitution G T downstream_gene_variant PACA-AU 3 10339023 10339023 single base substitution G T intron_variant PACA-AU 3 10341091 10341091 single base substitution A G downstream_gene_variant PACA-AU 3 10341091 10341091 single base substitution A G intron_variant PACA-AU 3 10342880 10342880 single base substitution T A 3_prime_UTR_variant PACA-AU 3 10342880 10342880 single base substitution T A downstream_gene_variant PACA-AU 3 10342880 10342880 single base substitution T A exon_variant PACA-AU 3 10342880 10342880 single base substitution T A intron_variant PACA-AU 3 10349169 10349169 insertion of <=200bp - A downstream_gene_variant PACA-AU 3 10349169 10349169 insertion of <=200bp - A intron_variant PACA-AU 3 10349169 10349169 insertion of <=200bp - A upstream_gene_variant PACA-AU 3 10357772 10357772 single base substitution G A downstream_gene_variant PACA-AU 3 10357772 10357772 single base substitution G A intron_variant PACA-AU 3 10357772 10357772 single base substitution G A upstream_gene_variant PACA-AU 3 10363452 10363452 single base substitution C G upstream_gene_variant PACA-CA 3 10330305 10330305 single base substitution C T downstream_gene_variant PACA-CA 3 10331009 10331009 single base substitution C T downstream_gene_variant PACA-CA 3 10333438 10333438 single base substitution T C downstream_gene_variant PACA-CA 3 10334661 10334661 insertion of <=200bp - T downstream_gene_variant PACA-CA 3 10335863 10335863 single base substitution C G intron_variant PACA-CA 3 10338227 10338227 single base substitution G A downstream_gene_variant PACA-CA 3 10338227 10338227 single base substitution G A intron_variant PACA-CA 3 10338327 10338327 single base substitution G C downstream_gene_variant PACA-CA 3 10338327 10338327 single base substitution G C intron_variant PACA-CA 3 10338573 10338573 single base substitution C T downstream_gene_variant PACA-CA 3 10338573 10338573 single base substitution C T intron_variant PACA-CA 3 10338681 10338681 single base substitution T C downstream_gene_variant PACA-CA 3 10338681 10338681 single base substitution T C intron_variant PACA-CA 3 10338827 10338827 single base substitution G A downstream_gene_variant PACA-CA 3 10338827 10338827 single base substitution G A intron_variant PACA-CA 3 10338894 10338894 single base substitution C T downstream_gene_variant PACA-CA 3 10338894 10338894 single base substitution C T intron_variant PACA-CA 3 10340925 10340925 single base substitution C G downstream_gene_variant PACA-CA 3 10340925 10340925 single base substitution C G intron_variant PACA-CA 3 10342158 10342158 single base substitution C T downstream_gene_variant PACA-CA 3 10342158 10342158 single base substitution C T intron_variant PACA-CA 3 10343628 10343628 deletion of <=200bp A - downstream_gene_variant PACA-CA 3 10343628 10343628 deletion of <=200bp A - intron_variant PACA-CA 3 10344444 10344444 single base substitution T C downstream_gene_variant PACA-CA 3 10344444 10344444 single base substitution T C intron_variant PACA-CA 3 10345357 10345357 single base substitution G C downstream_gene_variant PACA-CA 3 10345357 10345357 single base substitution G C exon_variant PACA-CA 3 10345357 10345357 single base substitution G C intron_variant PACA-CA 3 10349879 10349879 single base substitution T C downstream_gene_variant PACA-CA 3 10349879 10349879 single base substitution T C intron_variant PACA-CA 3 10349879 10349879 single base substitution T C upstream_gene_variant PACA-CA 3 10351519 10351519 single base substitution C T downstream_gene_variant PACA-CA 3 10351519 10351519 single base substitution C T intron_variant PACA-CA 3 10351519 10351519 single base substitution C T upstream_gene_variant PACA-CA 3 10353614 10353614 single base substitution G A downstream_gene_variant PACA-CA 3 10353614 10353614 single base substitution G A exon_variant PACA-CA 3 10353614 10353614 single base substitution G A intron_variant PACA-CA 3 10362929 10362929 single base substitution C G upstream_gene_variant PACA-CA 3 10363760 10363760 single base substitution G T upstream_gene_variant PAEN-AU 3 10351522 10351522 single base substitution A C downstream_gene_variant PAEN-AU 3 10351522 10351522 single base substitution A C intron_variant PAEN-AU 3 10351522 10351522 single base substitution A C upstream_gene_variant PAEN-AU 3 10360157 10360157 single base substitution C A downstream_gene_variant PAEN-AU 3 10360157 10360157 single base substitution C A intron_variant PAEN-AU 3 10360157 10360157 single base substitution C A upstream_gene_variant PAEN-AU 3 10365878 10365878 single base substitution C T upstream_gene_variant PBCA-DE 3 10336291 10336291 single base substitution G A intron_variant PBCA-DE 3 10342752 10342752 single base substitution T C 3_prime_UTR_variant PBCA-DE 3 10342752 10342752 single base substitution T C downstream_gene_variant PBCA-DE 3 10342752 10342752 single base substitution T C exon_variant PBCA-DE 3 10342752 10342752 single base substitution T C intron_variant PBCA-DE 3 10355614 10355614 single base substitution C T downstream_gene_variant PBCA-DE 3 10355614 10355614 single base substitution C T exon_variant PBCA-DE 3 10355614 10355614 single base substitution C T intron_variant PBCA-DE 3 10355614 10355614 single base substitution C T upstream_gene_variant PBCA-DE 3 10363417 10363417 deletion of <=200bp T - upstream_gene_variant PRAD-CA 3 10337292 10337292 single base substitution T G intron_variant PRAD-CA 3 10359035 10359035 single base substitution T C downstream_gene_variant PRAD-CA 3 10359035 10359035 single base substitution T C intron_variant PRAD-CA 3 10359035 10359035 single base substitution T C upstream_gene_variant PRAD-UK 3 10355594 10355594 single base substitution G A downstream_gene_variant PRAD-UK 3 10355594 10355594 single base substitution G A exon_variant PRAD-UK 3 10355594 10355594 single base substitution G A intron_variant PRAD-UK 3 10355594 10355594 single base substitution G A upstream_gene_variant PRAD-UK 3 10366880 10366880 single base substitution C G upstream_gene_variant PRAD-UK 3 10367424 10367424 single base substitution C A upstream_gene_variant RECA-EU 3 10347821 10347821 single base substitution T C intron_variant RECA-EU 3 10347821 10347821 single base substitution T C upstream_gene_variant RECA-EU 3 10348087 10348087 single base substitution G A intron_variant RECA-EU 3 10348087 10348087 single base substitution G A upstream_gene_variant RECA-EU 3 10348088 10348088 single base substitution C T intron_variant RECA-EU 3 10348088 10348088 single base substitution C T upstream_gene_variant RECA-EU 3 10351662 10351662 single base substitution G C downstream_gene_variant RECA-EU 3 10351662 10351662 single base substitution G C intron_variant RECA-EU 3 10351662 10351662 single base substitution G C upstream_gene_variant RECA-EU 3 10357951 10357951 single base substitution C A downstream_gene_variant RECA-EU 3 10357951 10357951 single base substitution C A intron_variant RECA-EU 3 10357951 10357951 single base substitution C A upstream_gene_variant RECA-EU 3 10357988 10357988 single base substitution C T downstream_gene_variant RECA-EU 3 10357988 10357988 single base substitution C T intron_variant RECA-EU 3 10357988 10357988 single base substitution C T upstream_gene_variant SKCA-BR 3 10329982 10329982 single base substitution G A downstream_gene_variant SKCA-BR 3 10336210 10336210 single base substitution G A intron_variant SKCA-BR 3 10337292 10337292 single base substitution T G intron_variant SKCA-BR 3 10340234 10340234 single base substitution C T downstream_gene_variant SKCA-BR 3 10340234 10340234 single base substitution C T intron_variant SKCA-BR 3 10342924 10342924 single base substitution A G 3_prime_UTR_variant SKCA-BR 3 10342924 10342924 single base substitution A G downstream_gene_variant SKCA-BR 3 10342924 10342924 single base substitution A G exon_variant SKCA-BR 3 10342924 10342924 single base substitution A G intron_variant SKCA-BR 3 10353781 10353781 single base substitution C T downstream_gene_variant SKCA-BR 3 10353781 10353781 single base substitution C T splice_region_variant SKCA-BR 3 10356053 10356053 single base substitution T G downstream_gene_variant SKCA-BR 3 10356053 10356053 single base substitution T G intron_variant SKCA-BR 3 10356053 10356053 single base substitution T G upstream_gene_variant SKCA-BR 3 10356103 10356103 single base substitution G T downstream_gene_variant SKCA-BR 3 10356103 10356103 single base substitution G T intron_variant SKCA-BR 3 10356103 10356103 single base substitution G T upstream_gene_variant SKCA-BR 3 10359888 10359888 single base substitution G A downstream_gene_variant SKCA-BR 3 10359888 10359888 single base substitution G A intron_variant SKCA-BR 3 10359888 10359888 single base substitution G A upstream_gene_variant SKCA-BR 3 10363420 10363421 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 3 10363643 10363643 single base substitution C T upstream_gene_variant SKCA-BR 3 10365077 10365077 single base substitution G A upstream_gene_variant SKCA-BR 3 10365397 10365397 insertion of <=200bp - GC upstream_gene_variant SKCA-BR 3 10365849 10365849 single base substitution G A upstream_gene_variant SKCA-BR 3 10367806 10367806 single base substitution C T upstream_gene_variant SKCM-US 3 10331519 10331519 single base substitution C T downstream_gene_variant SKCM-US 3 10346764 10346764 single base substitution C T exon_variant SKCM-US 3 10346764 10346764 single base substitution C T missense_variant A207T 619G>A SKCM-US 3 10346764 10346764 single base substitution C T missense_variant A221T 661G>A SKCM-US 3 10346764 10346764 single base substitution C T missense_variant A224T 670G>A SKCM-US 3 10346764 10346764 single base substitution C T missense_variant A267T 799G>A SKCM-US 3 10346764 10346764 single base substitution C T upstream_gene_variant SKCM-US 3 10346776 10346776 single base substitution C T exon_variant SKCM-US 3 10346776 10346776 single base substitution C T missense_variant D203N 607G>A SKCM-US 3 10346776 10346776 single base substitution C T missense_variant D217N 649G>A SKCM-US 3 10346776 10346776 single base substitution C T missense_variant D220N 658G>A SKCM-US 3 10346776 10346776 single base substitution C T missense_variant D263N 787G>A SKCM-US 3 10346776 10346776 single base substitution C T upstream_gene_variant SKCM-US 3 10353760 10353760 single base substitution G A downstream_gene_variant SKCM-US 3 10353760 10353760 single base substitution G A exon_variant SKCM-US 3 10353760 10353760 single base substitution G A synonymous_variant P113P 339C>T SKCM-US 3 10353760 10353760 single base substitution G A synonymous_variant P116P 348C>T SKCM-US 3 10353760 10353760 single base substitution G A synonymous_variant P159P 477C>T SKCM-US 3 10353760 10353760 single base substitution G A synonymous_variant P99P 297C>T SKCM-US 3 10357052 10357052 single base substitution G A downstream_gene_variant SKCM-US 3 10357052 10357052 single base substitution G A exon_variant SKCM-US 3 10357052 10357052 single base substitution G A synonymous_variant I25I 75C>T SKCM-US 3 10357052 10357052 single base substitution G A synonymous_variant I39I 117C>T SKCM-US 3 10357052 10357052 single base substitution G A synonymous_variant I42I 126C>T SKCM-US 3 10357052 10357052 single base substitution G A synonymous_variant I85I 255C>T SKCM-US 3 10357052 10357052 single base substitution G A upstream_gene_variant STAD-US 3 10331490 10331490 single base substitution C T downstream_gene_variant STAD-US 3 10346789 10346789 single base substitution A C exon_variant STAD-US 3 10346789 10346789 single base substitution A C missense_variant S198R 594T>G STAD-US 3 10346789 10346789 single base substitution A C missense_variant S212R 636T>G STAD-US 3 10346789 10346789 single base substitution A C missense_variant S215R 645T>G STAD-US 3 10346789 10346789 single base substitution A C missense_variant S258R 774T>G STAD-US 3 10346789 10346789 single base substitution A C upstream_gene_variant STAD-US 3 10354288 10354288 single base substitution G A downstream_gene_variant STAD-US 3 10354288 10354288 single base substitution G A exon_variant STAD-US 3 10354288 10354288 single base substitution G A synonymous_variant H100H 300C>T STAD-US 3 10354288 10354288 single base substitution G A synonymous_variant H143H 429C>T STAD-US 3 10354288 10354288 single base substitution G A synonymous_variant H83H 249C>T STAD-US 3 10354288 10354288 single base substitution G A synonymous_variant H97H 291C>T STAD-US 3 10354352 10354352 single base substitution G A downstream_gene_variant STAD-US 3 10354352 10354352 single base substitution G A exon_variant STAD-US 3 10354352 10354352 single base substitution G A missense_variant S122L 365C>T STAD-US 3 10354352 10354352 single base substitution G A missense_variant S62L 185C>T STAD-US 3 10354352 10354352 single base substitution G A missense_variant S76L 227C>T STAD-US 3 10354352 10354352 single base substitution G A missense_variant S79L 236C>T STAD-US 3 10357003 10357003 insertion of <=200bp - C downstream_gene_variant STAD-US 3 10357003 10357003 insertion of <=200bp - C exon_variant STAD-US 3 10357003 10357003 insertion of <=200bp - C splice_donor_variant STAD-US 3 10357003 10357003 insertion of <=200bp - C upstream_gene_variant STAD-US 3 10357004 10357004 insertion of <=200bp - C downstream_gene_variant STAD-US 3 10357004 10357004 insertion of <=200bp - C exon_variant STAD-US 3 10357004 10357004 insertion of <=200bp - C splice_donor_variant STAD-US 3 10357004 10357004 insertion of <=200bp - C upstream_gene_variant STAD-US 3 10357042 10357042 single base substitution G A downstream_gene_variant STAD-US 3 10357042 10357042 single base substitution G A exon_variant STAD-US 3 10357042 10357042 single base substitution G A missense_variant R29C 85C>T STAD-US 3 10357042 10357042 single base substitution G A missense_variant R43C 127C>T STAD-US 3 10357042 10357042 single base substitution G A missense_variant R46C 136C>T STAD-US 3 10357042 10357042 single base substitution G A missense_variant R89C 265C>T STAD-US 3 10357042 10357042 single base substitution G A upstream_gene_variant UCEC-US 3 10331784 10331784 single base substitution G A downstream_gene_variant UCEC-US 3 10331837 10331837 single base substitution G T downstream_gene_variant UCEC-US 3 10334501 10334501 single base substitution C T downstream_gene_variant UCEC-US 3 10334515 10334515 single base substitution C T downstream_gene_variant UCEC-US 3 10334703 10334703 single base substitution C T downstream_gene_variant UCEC-US 3 10335033 10335033 insertion of <=200bp - CATG intron_variant UCEC-US 3 10345786 10345786 single base substitution T C downstream_gene_variant UCEC-US 3 10345786 10345786 single base substitution T C exon_variant UCEC-US 3 10345786 10345786 single base substitution T C missense_variant K246R 737A>G UCEC-US 3 10345786 10345786 single base substitution T C missense_variant K260R 779A>G UCEC-US 3 10345786 10345786 single base substitution T C missense_variant K263R 788A>G UCEC-US 3 10345786 10345786 single base substitution T C missense_variant K306R 917A>G UCEC-US 3 10345799 10345799 single base substitution T A exon_variant UCEC-US 3 10345799 10345799 single base substitution T A stop_gained K242* 724A>T UCEC-US 3 10345799 10345799 single base substitution T A stop_gained K256* 766A>T UCEC-US 3 10345799 10345799 single base substitution T A stop_gained K259* 775A>T UCEC-US 3 10345799 10345799 single base substitution T A stop_gained K302* 904A>T UCEC-US 3 10345850 10345850 single base substitution G A exon_variant UCEC-US 3 10345850 10345850 single base substitution G A missense_variant R225C 673C>T UCEC-US 3 10345850 10345850 single base substitution G A missense_variant R239C 715C>T UCEC-US 3 10345850 10345850 single base substitution G A missense_variant R242C 724C>T UCEC-US 3 10345850 10345850 single base substitution G A missense_variant R285C 853C>T UCEC-US 3 10346791 10346791 single base substitution T G exon_variant UCEC-US 3 10346791 10346791 single base substitution T G missense_variant S198R 592A>C UCEC-US 3 10346791 10346791 single base substitution T G missense_variant S212R 634A>C UCEC-US 3 10346791 10346791 single base substitution T G missense_variant S215R 643A>C UCEC-US 3 10346791 10346791 single base substitution T G missense_variant S258R 772A>C UCEC-US 3 10346791 10346791 single base substitution T G upstream_gene_variant UCEC-US 3 10346828 10346828 single base substitution G A exon_variant UCEC-US 3 10346828 10346828 single base substitution G A synonymous_variant D185D 555C>T UCEC-US 3 10346828 10346828 single base substitution G A synonymous_variant D199D 597C>T UCEC-US 3 10346828 10346828 single base substitution G A synonymous_variant D202D 606C>T UCEC-US 3 10346828 10346828 single base substitution G A synonymous_variant D245D 735C>T UCEC-US 3 10346828 10346828 single base substitution G A upstream_gene_variant UCEC-US 3 10353685 10353685 single base substitution G T downstream_gene_variant UCEC-US 3 10353685 10353685 single base substitution G T exon_variant UCEC-US 3 10353685 10353685 single base substitution G T synonymous_variant G124G 372C>A UCEC-US 3 10353685 10353685 single base substitution G T synonymous_variant G138G 414C>A UCEC-US 3 10353685 10353685 single base substitution G T synonymous_variant G141G 423C>A UCEC-US 3 10353685 10353685 single base substitution G T synonymous_variant G184G 552C>A UCEC-US 3 10354272 10354272 single base substitution C T downstream_gene_variant UCEC-US 3 10354272 10354272 single base substitution C T exon_variant UCEC-US 3 10354272 10354272 single base substitution C T missense_variant D103N 307G>A UCEC-US 3 10354272 10354272 single base substitution C T missense_variant D106N 316G>A UCEC-US 3 10354272 10354272 single base substitution C T missense_variant D149N 445G>A UCEC-US 3 10354272 10354272 single base substitution C T missense_variant D89N 265G>A UCEC-US 3 10357052 10357052 single base substitution G T downstream_gene_variant UCEC-US 3 10357052 10357052 single base substitution G T exon_variant UCEC-US 3 10357052 10357052 single base substitution G T synonymous_variant I25I 75C>A UCEC-US 3 10357052 10357052 single base substitution G T synonymous_variant I39I 117C>A UCEC-US 3 10357052 10357052 single base substitution G T synonymous_variant I42I 126C>A UCEC-US 3 10357052 10357052 single base substitution G T synonymous_variant I85I 255C>A UCEC-US 3 10357052 10357052 single base substitution G T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 082T COSM1730909 c.115A>G p.I39V Substitution - Missense 3:10315370-10315370 - TCGA-DD-A4NV-01 COSM4916414 c.548C>T p.A183V Substitution - Missense 3:10305595-10305595 - PD4602a COSM164234 c.661G>A p.A221T Substitution - Missense 3:10305080-10305080 - 2492726 COSM5724687 c.766A>G p.K256E Substitution - Missense 3:10304115-10304115 - TCGA-GL-8500-01 COSM3992616 c.947A>G p.E316G Substitution - Missense 3:10301283-10301283 - SA071 COSM213280 c.458G>C p.C153S Substitution - Missense 3:10305685-10305685 - TCGA-61-2009-01 COSM72572 c.128G>A p.R43H Substitution - Missense 3:10315357-10315357 - EGC15 COSM4111964 c.127C>T p.R43C Substitution - Missense 3:10315358-10315358 - TCGA-18-3415-01 COSM727481 c.520C>T p.Q174* Substitution - Nonsense 3:10305623-10305623 - SNU-175 COSM2916138 c.558C>A p.G186G Substitution - coding silent 3:10305585-10305585 - sysucc-274T COSM5476412 c.450+1G>A p.? Unknown 3:10311964-10311964 - cSCCP4 COSM138357 c.227C>T p.S76L Substitution - Missense 3:10312668-10312668 - B35 COSM1752761 c.60G>C p.Q20H Substitution - Missense 3:10315425-10315425 - L363 COSM1236141 c.241C>T p.R81W Substitution - Missense 3:10312654-10312654 - TCGA-AP-A0LT-01 COSM1035908 c.634A>C p.S212R Substitution - Missense 3:10305107-10305107 - TCGA-F1-6177-01 COSM4111964 c.127C>T p.R43C Substitution - Missense 3:10315358-10315358 - TCGA-BS-A0UV-01 COSM1035909 c.597C>T p.D199D Substitution - coding silent 3:10305144-10305144 - TCGA-BS-A0UJ-01 COSM1035905 c.779A>G p.K260R Substitution - Missense 3:10304102-10304102 - TCGA-66-2785-01 COSM727482 c.883G>C p.G295R Substitution - Missense 3:10301347-10301347 - TCGA-DK-A1A6-01 COSM1308342 c.201C>T p.H67H Substitution - coding silent 3:10312694-10312694 - SC_9076 COSM3584773 c.117C>T p.I39I Substitution - coding silent 3:10315368-10315368 - T3254 COSM4724479 c.646C>T p.R216* Substitution - Nonsense 3:10305095-10305095 - 019T COSM1727934 c.566A>G p.N189S Substitution - Missense 3:10305577-10305577 - TCGA-DA-A1HV-06 COSM3584771 c.649G>A p.D217N Substitution - Missense 3:10305092-10305092 - TCGA-CG-4474-01 COSM4111963 c.291C>T p.H97H Substitution - coding silent 3:10312604-10312604 - TCGA-CA-6717-01 COSM1417491 c.927C>T p.S309S Substitution - coding silent 3:10301303-10301303 - 07-P075 COSM4583756 c.547G>C p.A183P Substitution - Missense 3:10305596-10305596 - TCGA-AX-A0J1-01 COSM1035907 c.715C>T p.R239C Substitution - Missense 3:10304166-10304166 - B35-Tumor COSM1752761 c.60G>C p.Q20H Substitution - Missense 3:10315425-10315425 - sysucc-627T COSM5468058 c.503T>C p.I168T Substitution - Missense 3:10305640-10305640 - B104-0-Tumor COSM4005218 c.708+3C>T p.? Unknown 3:10305030-10305030 - LIM1899 COSM4640472 c.598G>T p.G200C Substitution - Missense 3:10305143-10305143 - TCGA-BH-A0BV-01 COSM445238 c.292G>A p.E98K Substitution - Missense 3:10312603-10312603 - 6115224 COSM5568708 c.233C>T p.S78F Substitution - Missense 3:10312662-10312662 - PD4937a COSM164235 c.151G>A p.A51T Substitution - Missense 3:10315334-10315334 - BD72T COSM5511882 c.874T>A p.S292T Substitution - Missense 3:10301356-10301356 - TCGA-GV-A3JW-01 COSM1308341 c.946G>C p.E316Q Substitution - Missense 3:10301284-10301284 - TCGA-D8-A140-01 COSM445239 c.258G>A p.W86* Substitution - Nonsense 3:10312637-10312637 - TCGA-AP-A051-01 COSM1035910 c.414C>A p.G138G Substitution - coding silent 3:10312001-10312001 - TCGA-CJ-4902-01 COSM479184 c.243G>T p.R81R Substitution - coding silent 3:10312652-10312652 - TCGA-AC-A23H-01 COSM3845708 c.880G>A p.D294N Substitution - Missense 3:10301350-10301350 - TCGA-EE-A3JI-06 COSM164234 c.661G>A p.A221T Substitution - Missense 3:10305080-10305080 - CRC-02T COSM72572 c.128G>A p.R43H Substitution - Missense 3:10315357-10315357 - TCGA-B0-5098-01 COSM1035909 c.597C>T p.D199D Substitution - coding silent 3:10305144-10305144 - TCGA-BR-8680-01 COSM138357 c.227C>T p.S76L Substitution - Missense 3:10312668-10312668 - 2492724 COSM5724687 c.766A>G p.K256E Substitution - Missense 3:10304115-10304115 - TCGA-BG-A0M3-01 COSM1035911 c.307G>A p.D103N Substitution - Missense 3:10312588-10312588 - CSCC-35-T COSM4453049 c.245A>T p.K82I Substitution - Missense 3:10312650-10312650 - TCGA-BR-4257-01 COSM4111962 c.636T>G p.S212R Substitution - Missense 3:10305105-10305105 - pfg019T COSM1642040 c.716G>A p.R239H Substitution - Missense 3:10304165-10304165 - sysucc-1370T COSM1035909 c.597C>T p.D199D Substitution - coding silent 3:10305144-10305144 - 2492725 COSM5724687 c.766A>G p.K256E Substitution - Missense 3:10304115-10304115 - TCGA-ER-A2NC-06 COSM3584772 c.339C>T p.P113P Substitution - coding silent 3:10312076-10312076 - MOLT-4 COSM1669965 c.798G>A p.W266* Substitution - Nonsense 3:10304083-10304083 - TCGA-A5-A0GM-01 COSM1035906 c.766A>T p.K256* Substitution - Nonsense 3:10304115-10304115 - PD7396a COSM3720132 c.4G>T p.V2L Substitution - Missense 3:10318094-10318094 - TCGA-CM-6169-01 COSM1417493 c.630G>A p.A210A Substitution - coding silent 3:10305111-10305111 - TCGA-AP-A0LM-01 COSM1035912 c.117C>A p.I39I Substitution - coding silent 3:10315368-10315368 - TCGA-42-2582-01 COSM1327142 c.790G>C p.V264L Substitution - Missense 3:10304091-10304091 - TCGA-ER-A193-06 COSM3584773 c.117C>T p.I39I Substitution - coding silent 3:10315368-10315368 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.166647;Hs.166676;Hs.166924 3p25-p24 600152 2431120|CGAP|BC002634|A/G|non-coding||1088|Validated; 2431120|CGAP|BC091506|A/G|non-coding||1083|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.S212R c.636T>G 3 10346789 STAD C G IntronicSNV . c.4-1149G>C 3 10360927 BRCA C G Missense p.C153S c.458G>C 3 10347369 BRCA C G Missense p.E316Q c.946G>C 3 10342968 BLCA C G Missense p.G71R c.211G>C 3 10354368 CM C G Missense p.W86C c.258G>C 3 10354321 LUAD C T IntronicSNV . c.165-1200G>A 3 10355614 MB C T IntronicSNV . c.585-47G>A 3 10346887 CM C T Missense p.A221T c.661G>A 3 10346764 BRCA C T Missense p.A221T c.661G>A 3 10346764 CM C T Missense p.A51T c.151G>A 3 10357018 BRCA C T Missense p.D103N c.307G>A 3 10354272 UCEC C T Missense p.D217N c.649G>A 3 10346776 CM C T Missense p.E98K c.292G>A 3 10354287 BRCA C T Missense p.R239H c.716G>A 3 10345849 STAD C T Missense p.R43H c.128G>A 3 10357041 OV C T Nonsense p.W86* c.258G>A 3 10354321 BRCA G A Missense p.R43C c.127C>T 3 10357042 STAD G A Nonsense p.Q174* c.520C>T 3 10347307 LUSC G A Synonymous p.C31C c.93C>T 3 10357076 COREAD G A Synonymous p.H67H c.201C>T 3 10354378 BLCA G A Synonymous p.H97H c.291C>T 3 10354288 STAD G A Synonymous p.I39I c.117C>T 3 10357052 CM G A Synonymous p.P113P c.339C>T 3 10353760 CM G C IntronicSNV . c.709-34C>G 3 10345890 PIA T A Nonsense p.K256* c.766A>T 3 10345799 UCEC T C 3-UTRSNV . c.966+196A>G 3 10342752 MB T G Missense p.S212R c.634A>C 3 10346791 UCEC