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 8 145579212 145579212 + Silent SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr8:145579212G>A c.1599C>T c.(1597-1599)ctC>ctT p.L533L BLCA 8 145579794 145579794 + Missense_Mutation SNP G G T TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr8:145579794G>T c.1306C>A c.(1306-1308)Cag>Aag p.Q436K BLCA 8 145580113 145580113 + Silent SNP G G A TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr8:145580113G>A c.1072C>T c.(1072-1074)Cta>Tta p.L358L BLCA 8 145582012 145582012 + Silent SNP C C G TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr8:145582012C>G c.96G>C c.(94-96)ccG>ccC p.P32P BLCA 8 145582012 145582012 + Silent SNP C C T TCGA-FD-A43X-01A-11D-A23U-08 TCGA-FD-A43X-10A-01D-A23U-08 g.chr8:145582012C>T c.96G>A c.(94-96)ccG>ccA p.P32P BLCA 8 145582067 145582067 + Missense_Mutation SNP C C A TCGA-GV-A3QF-01A-31D-A22Z-08 TCGA-GV-A3QF-10A-01D-A22Z-08 g.chr8:145582067C>A c.41G>T c.(40-42)cGg>cTg p.R14L BRCA 8 145580146 145580146 + Nonsense_Mutation SNP G G A TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr8:145580146G>A c.1039C>T c.(1039-1041)Cga>Tga p.R347* COAD 8 145579677 145579677 + Missense_Mutation SNP G G T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr8:145579677G>T c.1423C>A c.(1423-1425)Ctg>Atg p.L475M COAD 8 145579773 145579773 + Nonsense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr8:145579773G>A c.1327C>T c.(1327-1329)Cga>Tga p.R443* COAD 8 145579783 145579783 + Silent SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr8:145579783G>A c.1317C>T c.(1315-1317)tgC>tgT p.C439C COAD 8 145579962 145579962 + Missense_Mutation SNP C C T TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr8:145579962C>T c.1223G>A c.(1222-1224)cGg>cAg p.R408Q COAD 8 145579964 145579964 + Silent SNP A A G TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr8:145579964A>G c.1221T>C c.(1219-1221)tgT>tgC p.C407C COAD 8 145579967 145579967 + Silent SNP T T C TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr8:145579967T>C c.1218A>G c.(1216-1218)ccA>ccG p.P406P COAD 8 145580513 145580513 + Nonsense_Mutation SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr8:145580513C>T c.834G>A c.(832-834)tgG>tgA p.W278* COADREAD 8 145579677 145579677 + Missense_Mutation SNP G G T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr8:145579677G>T c.1423C>A c.(1423-1425)Ctg>Atg p.L475M COADREAD 8 145579773 145579773 + Nonsense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr8:145579773G>A c.1327C>T c.(1327-1329)Cga>Tga p.R443* COADREAD 8 145579783 145579783 + Silent SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr8:145579783G>A c.1317C>T c.(1315-1317)tgC>tgT p.C439C COADREAD 8 145579962 145579962 + Missense_Mutation SNP C C T TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr8:145579962C>T c.1223G>A c.(1222-1224)cGg>cAg p.R408Q COADREAD 8 145579964 145579964 + Silent SNP A A G TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr8:145579964A>G c.1221T>C c.(1219-1221)tgT>tgC p.C407C COADREAD 8 145579967 145579967 + Silent SNP T T C TCGA-A6-6651-01A-21D-1835-10 TCGA-A6-6651-10A-01D-1835-10 g.chr8:145579967T>C c.1218A>G c.(1216-1218)ccA>ccG p.P406P COADREAD 8 145580513 145580513 + Nonsense_Mutation SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr8:145580513C>T c.834G>A c.(832-834)tgG>tgA p.W278* ESCA 8 145580145 145580145 + Missense_Mutation SNP C C T TCGA-VR-A8EX-01A-11D-A36J-09 TCGA-VR-A8EX-10A-01D-A36M-09 g.chr8:145580145C>T c.1040G>A c.(1039-1041)cGa>cAa p.R347Q GBM 8 145579316 145579316 + Missense_Mutation SNP C C G TCGA-32-1977-01A-01D-1353-08 TCGA-32-1977-10C-01D-1353-08 g.chr8:145579316C>G c.1495G>C c.(1495-1497)Ggc>Cgc p.G499R GBM 8 145581939 145581939 + Missense_Mutation SNP G G A TCGA-26-1439-01A-01D-1353-08 TCGA-26-1439-10A-01D-1353-08 g.chr8:145581939G>A c.169C>T c.(169-171)Ccc>Tcc p.P57S GBMLGG 8 145579316 145579316 + Missense_Mutation SNP C C G TCGA-32-1977-01A-01D-1353-08 TCGA-32-1977-10C-01D-1353-08 g.chr8:145579316C>G c.1495G>C c.(1495-1497)Ggc>Cgc p.G499R GBMLGG 8 145580132 145580132 + Silent SNP G G A TCGA-P5-A5EW-01A-11D-A27K-08 TCGA-P5-A5EW-10A-01D-A27N-08 g.chr8:145580132G>A c.1053C>T c.(1051-1053)ccC>ccT p.P351P GBMLGG 8 145581939 145581939 + Missense_Mutation SNP G G A TCGA-26-1439-01A-01D-1353-08 TCGA-26-1439-10A-01D-1353-08 g.chr8:145581939G>A c.169C>T c.(169-171)Ccc>Tcc p.P57S HNSC 8 145579649 145579649 + Missense_Mutation SNP C C T TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr8:145579649C>T c.1451G>A c.(1450-1452)cGg>cAg p.R484Q HNSC 8 145579649 145579649 + Missense_Mutation SNP C C T TCGA-H7-A76A-01A-51D-A34J-08 TCGA-H7-A76A-10A-01D-A34M-08 g.chr8:145579649C>T c.1451G>A c.(1450-1452)cGg>cAg p.R484Q HNSC 8 145580332 145580332 + Silent SNP G G A TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr8:145580332G>A c.921C>T c.(919-921)acC>acT p.T307T HNSC 8 145581347 145581347 + Missense_Mutation SNP C C A TCGA-UF-A71D-01A-12D-A34J-08 TCGA-UF-A71D-10B-01D-A34M-08 g.chr8:145581347C>A c.516G>T c.(514-516)aaG>aaT p.K172N HNSC 8 145582012 145582012 + Silent SNP C C G TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr8:145582012C>G c.96G>C c.(94-96)ccG>ccC p.P32P KIPAN 8 145579793 145579793 + Missense_Mutation SNP T T C TCGA-G7-6796-01A-11D-1961-08 TCGA-G7-6796-10A-01D-1962-08 g.chr8:145579793T>C c.1307A>G c.(1306-1308)cAg>cGg p.Q436R KIRP 8 145579793 145579793 + Missense_Mutation SNP T T C TCGA-G7-6796-01A-11D-1961-08 TCGA-G7-6796-10A-01D-1962-08 g.chr8:145579793T>C c.1307A>G c.(1306-1308)cAg>cGg p.Q436R LGG 8 145580132 145580132 + Silent SNP G G A TCGA-P5-A5EW-01A-11D-A27K-08 TCGA-P5-A5EW-10A-01D-A27N-08 g.chr8:145580132G>A c.1053C>T c.(1051-1053)ccC>ccT p.P351P LIHC 8 145580146 145580146 + Missense_Mutation SNP G G C TCGA-G3-A3CH-01A-11D-A22F-10 TCGA-G3-A3CH-11A-11D-A22F-10 g.chr8:145580146G>C c.1039C>G c.(1039-1041)Cga>Gga p.R347G LUAD 8 145579332 145579332 + Silent SNP C C A TCGA-55-8614-01A-11D-2393-08 TCGA-55-8614-10A-01D-2393-08 g.chr8:145579332C>A c.1479G>T c.(1477-1479)gtG>gtT p.V493V LUAD 8 145579642 145579642 + Silent SNP T T C TCGA-97-A4M3-01A-11D-A24P-08 TCGA-97-A4M3-10A-01D-A24P-08 g.chr8:145579642T>C c.1458A>G c.(1456-1458)acA>acG p.T486T LUAD 8 145579728 145579728 + Missense_Mutation SNP C C G TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr8:145579728C>G c.1372G>C c.(1372-1374)Gag>Cag p.E458Q LUAD 8 145581359 145581359 + Silent SNP G G A TCGA-49-4486-01A-01D-1265-08 TCGA-49-4486-11A-01D-1265-08 g.chr8:145581359G>A c.504C>T c.(502-504)ggC>ggT p.G168G LUSC 8 145579815 145579815 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr8:145579815C>T c.1285G>A c.(1285-1287)Gag>Aag p.E429K PAAD 8 145580129 145580129 + Silent SNP T T A TCGA-HV-AA8V-01A-11D-A40W-08 TCGA-HV-AA8V-10A-01D-A40W-08 g.chr8:145580129T>A c.1056A>T c.(1054-1056)ggA>ggT p.G352G PAAD 8 145580308 145580308 + Silent SNP G G A TCGA-3A-A9IZ-01A-12D-A40W-08 TCGA-3A-A9IZ-10A-01D-A40W-08 g.chr8:145580308G>A c.945C>T c.(943-945)ccC>ccT p.P315P PRAD 8 145579637 145579637 + Missense_Mutation SNP C C A TCGA-ZG-A9M4-01A-11D-A41K-08 TCGA-ZG-A9M4-10A-01D-A41N-08 g.chr8:145579637C>A c.1463G>T c.(1462-1464)aGc>aTc p.S488I PRAD 8 145579796 145579796 + Missense_Mutation SNP G G T TCGA-J4-A67L-01A-11D-A30E-08 TCGA-J4-A67L-10A-01D-A30H-08 g.chr8:145579796G>T c.1304C>A c.(1303-1305)aCc>aAc p.T435N SKCM 8 145579332 145579333 + Frame_Shift_Del DEL CA CA - TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr8:145579332_145579333delCA c.1478_1479delTG c.(1477-1479)gtgfs p.V493fs SKCM 8 145579670 145579670 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr8:145579670G>A c.1430C>T c.(1429-1431)tCt>tTt p.S477F SKCM 8 145579751 145579751 + Missense_Mutation SNP T T G TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr8:145579751T>G c.1349A>C c.(1348-1350)cAg>cCg p.Q450P SKCM 8 145579875 145579875 + Splice_Site SNP C C T TCGA-DA-A1IA-06A-11D-A196-08 TCGA-DA-A1IA-10A-01D-A198-08 g.chr8:145579875C>T c.e8-1 SKCM 8 145580011 145580011 + Missense_Mutation SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr8:145580011G>A c.1174C>T c.(1174-1176)Cgt>Tgt p.R392C SKCM 8 145580114 145580114 + Silent SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr8:145580114G>A c.1071C>T c.(1069-1071)agC>agT p.S357S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 8 145579794 145579794 single base substitution G T downstream_gene_variant BLCA-US 8 145579794 145579794 single base substitution G T exon_variant BLCA-US 8 145579794 145579794 single base substitution G T intron_variant BLCA-US 8 145579794 145579794 single base substitution G T missense_variant Q430K 1288C>A BLCA-US 8 145579794 145579794 single base substitution G T missense_variant Q436K 1306C>A BLCA-US 8 145580113 145580113 single base substitution G A downstream_gene_variant BLCA-US 8 145580113 145580113 single base substitution G A exon_variant BLCA-US 8 145580113 145580113 single base substitution G A synonymous_variant L352L 1054C>T BLCA-US 8 145580113 145580113 single base substitution G A synonymous_variant L358L 1072C>T BLCA-US 8 145583069 145583069 single base substitution A G upstream_gene_variant BLCA-US 8 145583548 145583548 single base substitution C T upstream_gene_variant BLCA-US 8 145583820 145583820 single base substitution C T upstream_gene_variant BLCA-US 8 145583976 145583976 single base substitution G A upstream_gene_variant BRCA-EU 8 145574723 145574723 single base substitution C T downstream_gene_variant BRCA-EU 8 145574892 145574892 single base substitution A C downstream_gene_variant BRCA-EU 8 145575292 145575292 single base substitution G T downstream_gene_variant BRCA-EU 8 145576818 145576818 single base substitution C A downstream_gene_variant BRCA-EU 8 145577332 145577332 single base substitution G A downstream_gene_variant BRCA-EU 8 145577603 145577603 single base substitution C T downstream_gene_variant BRCA-EU 8 145579728 145579728 single base substitution C A downstream_gene_variant BRCA-EU 8 145579728 145579728 single base substitution C A exon_variant BRCA-EU 8 145579728 145579728 single base substitution C A intron_variant BRCA-EU 8 145579728 145579728 single base substitution C A stop_gained E452* 1354G>T BRCA-EU 8 145579728 145579728 single base substitution C A stop_gained E458* 1372G>T BRCA-EU 8 145579799 145579799 insertion of <=200bp - A downstream_gene_variant BRCA-EU 8 145579799 145579799 insertion of <=200bp - A exon_variant BRCA-EU 8 145579799 145579799 insertion of <=200bp - A frameshift_variant L428F? BRCA-EU 8 145579799 145579799 insertion of <=200bp - A frameshift_variant L434F? BRCA-EU 8 145579799 145579799 insertion of <=200bp - A intron_variant BRCA-EU 8 145580745 145580745 single base substitution T C downstream_gene_variant BRCA-EU 8 145580745 145580745 single base substitution T C exon_variant BRCA-EU 8 145580745 145580745 single base substitution T C missense_variant K220E 658A>G BRCA-EU 8 145580745 145580745 single base substitution T C missense_variant K226E 676A>G BRCA-EU 8 145580745 145580745 single base substitution T C upstream_gene_variant BRCA-EU 8 145581897 145581897 single base substitution G A exon_variant BRCA-EU 8 145581897 145581897 single base substitution G A missense_variant P71S 211C>T BRCA-EU 8 145581897 145581897 single base substitution G A upstream_gene_variant BRCA-EU 8 145583670 145583670 single base substitution C T upstream_gene_variant BRCA-EU 8 145584850 145584850 single base substitution G A upstream_gene_variant BRCA-EU 8 145584892 145584892 single base substitution G A upstream_gene_variant BRCA-EU 8 145585409 145585409 single base substitution T G upstream_gene_variant BRCA-EU 8 145585759 145585759 single base substitution A G upstream_gene_variant BRCA-EU 8 145585765 145585765 single base substitution C T upstream_gene_variant BRCA-US 8 145578296 145578296 single base substitution A G downstream_gene_variant BRCA-US 8 145580146 145580146 single base substitution G A downstream_gene_variant BRCA-US 8 145580146 145580146 single base substitution G A exon_variant BRCA-US 8 145580146 145580146 single base substitution G A stop_gained R341* 1021C>T BRCA-US 8 145580146 145580146 single base substitution G A stop_gained R347* 1039C>T BRCA-US 8 145580670 145580670 single base substitution G T downstream_gene_variant BRCA-US 8 145580670 145580670 single base substitution G T exon_variant BRCA-US 8 145580670 145580670 single base substitution G T missense_variant L245M 733C>A BRCA-US 8 145580670 145580670 single base substitution G T missense_variant L251M 751C>A BRCA-US 8 145580670 145580670 single base substitution G T upstream_gene_variant BRCA-US 8 145583494 145583494 single base substitution C G upstream_gene_variant BRCA-US 8 145584130 145584130 deletion of <=200bp C - upstream_gene_variant BRCA-US 8 145584626 145584626 single base substitution A G upstream_gene_variant BTCA-JP 8 145577204 145577204 single base substitution C T downstream_gene_variant BTCA-JP 8 145577627 145577627 single base substitution C A downstream_gene_variant BTCA-JP 8 145578296 145578296 single base substitution A G downstream_gene_variant BTCA-JP 8 145579677 145579677 single base substitution G A downstream_gene_variant BTCA-JP 8 145579677 145579677 single base substitution G A exon_variant BTCA-JP 8 145579677 145579677 single base substitution G A intron_variant BTCA-JP 8 145579677 145579677 single base substitution G A synonymous_variant L469L 1405C>T BTCA-JP 8 145579677 145579677 single base substitution G A synonymous_variant L475L 1423C>T BTCA-JP 8 145580579 145580579 single base substitution G T downstream_gene_variant BTCA-JP 8 145580579 145580579 single base substitution G T exon_variant BTCA-JP 8 145580579 145580579 single base substitution G T splice_region_variant BTCA-JP 8 145580579 145580579 single base substitution G T upstream_gene_variant BTCA-JP 8 145580806 145580806 single base substitution G T downstream_gene_variant BTCA-JP 8 145580806 145580806 single base substitution G T exon_variant BTCA-JP 8 145580806 145580806 single base substitution G T intron_variant BTCA-JP 8 145580806 145580806 single base substitution G T upstream_gene_variant BTCA-JP 8 145580809 145580809 single base substitution G C downstream_gene_variant BTCA-JP 8 145580809 145580809 single base substitution G C exon_variant BTCA-JP 8 145580809 145580809 single base substitution G C intron_variant BTCA-JP 8 145580809 145580809 single base substitution G C upstream_gene_variant BTCA-JP 8 145581291 145581291 single base substitution T C exon_variant BTCA-JP 8 145581291 145581291 single base substitution T C missense_variant N191S 572A>G BTCA-JP 8 145581291 145581291 single base substitution T C upstream_gene_variant BTCA-JP 8 145581557 145581557 single base substitution G A exon_variant BTCA-JP 8 145581557 145581557 single base substitution G A intron_variant BTCA-JP 8 145581557 145581557 single base substitution G A upstream_gene_variant BTCA-JP 8 145582976 145582976 single base substitution G T intron_variant BTCA-JP 8 145582976 145582976 single base substitution G T upstream_gene_variant BTCA-JP 8 145584470 145584470 single base substitution C T upstream_gene_variant CESC-US 8 145584267 145584267 single base substitution G A upstream_gene_variant COAD-US 8 145579773 145579773 single base substitution G A downstream_gene_variant COAD-US 8 145579773 145579773 single base substitution G A exon_variant COAD-US 8 145579773 145579773 single base substitution G A intron_variant COAD-US 8 145579773 145579773 single base substitution G A stop_gained R437* 1309C>T COAD-US 8 145579773 145579773 single base substitution G A stop_gained R443* 1327C>T COAD-US 8 145579783 145579783 single base substitution G A downstream_gene_variant COAD-US 8 145579783 145579783 single base substitution G A exon_variant COAD-US 8 145579783 145579783 single base substitution G A intron_variant COAD-US 8 145579783 145579783 single base substitution G A synonymous_variant C433C 1299C>T COAD-US 8 145579783 145579783 single base substitution G A synonymous_variant C439C 1317C>T COAD-US 8 145579962 145579962 single base substitution C T downstream_gene_variant COAD-US 8 145579962 145579962 single base substitution C T missense_variant R402Q 1205G>A COAD-US 8 145579962 145579962 single base substitution C T missense_variant R408Q 1223G>A COAD-US 8 145579962 145579962 single base substitution C T splice_region_variant COAD-US 8 145580513 145580513 single base substitution C T downstream_gene_variant COAD-US 8 145580513 145580513 single base substitution C T exon_variant COAD-US 8 145580513 145580513 single base substitution C T stop_gained W272* 816G>A COAD-US 8 145580513 145580513 single base substitution C T stop_gained W278* 834G>A COAD-US 8 145580578 145580578 deletion of <=200bp G - downstream_gene_variant COAD-US 8 145580578 145580578 deletion of <=200bp G - exon_variant COAD-US 8 145580578 145580578 deletion of <=200bp G - splice_region_variant COAD-US 8 145580578 145580578 deletion of <=200bp G - upstream_gene_variant COAD-US 8 145583387 145583387 single base substitution G A upstream_gene_variant COAD-US 8 145584313 145584313 single base substitution G A upstream_gene_variant COAD-US 8 145584313 145584313 single base substitution G T upstream_gene_variant COAD-US 8 145584337 145584337 single base substitution G A upstream_gene_variant COAD-US 8 145584505 145584505 single base substitution A G upstream_gene_variant COCA-CN 8 145577259 145577259 single base substitution C T downstream_gene_variant COCA-CN 8 145577916 145577916 single base substitution C T downstream_gene_variant COCA-CN 8 145579931 145579931 single base substitution C G downstream_gene_variant COCA-CN 8 145579931 145579931 single base substitution C G intron_variant COCA-CN 8 145579932 145579932 single base substitution C T downstream_gene_variant COCA-CN 8 145579932 145579932 single base substitution C T intron_variant COCA-CN 8 145579936 145579936 single base substitution C T downstream_gene_variant COCA-CN 8 145579936 145579936 single base substitution C T intron_variant COCA-CN 8 145579943 145579943 single base substitution C A downstream_gene_variant COCA-CN 8 145579943 145579943 single base substitution C A intron_variant COCA-CN 8 145579950 145579950 single base substitution G A downstream_gene_variant COCA-CN 8 145579950 145579950 single base substitution G A intron_variant COCA-CN 8 145579953 145579953 single base substitution T A downstream_gene_variant COCA-CN 8 145579953 145579953 single base substitution T A splice_region_variant COCA-CN 8 145579954 145579954 single base substitution G A downstream_gene_variant COCA-CN 8 145579954 145579954 single base substitution G A splice_region_variant COCA-CN 8 145581739 145581739 single base substitution A C exon_variant COCA-CN 8 145581739 145581739 single base substitution A C missense_variant I123M 369T>G COCA-CN 8 145581739 145581739 single base substitution A C upstream_gene_variant ESAD-UK 8 145575060 145575060 single base substitution G C downstream_gene_variant ESAD-UK 8 145576382 145576382 single base substitution C T downstream_gene_variant ESAD-UK 8 145576408 145576408 single base substitution C A downstream_gene_variant ESAD-UK 8 145577356 145577356 single base substitution G A downstream_gene_variant ESAD-UK 8 145577853 145577853 single base substitution C T downstream_gene_variant ESAD-UK 8 145578254 145578254 single base substitution G A downstream_gene_variant ESAD-UK 8 145578666 145578666 single base substitution G A downstream_gene_variant ESAD-UK 8 145579419 145579419 single base substitution G T downstream_gene_variant ESAD-UK 8 145579419 145579419 single base substitution G T intron_variant ESAD-UK 8 145579868 145579868 single base substitution T C downstream_gene_variant ESAD-UK 8 145579868 145579868 single base substitution T C exon_variant ESAD-UK 8 145579868 145579868 single base substitution T C intron_variant ESAD-UK 8 145579868 145579868 single base substitution T C missense_variant E405G 1214A>G ESAD-UK 8 145579868 145579868 single base substitution T C missense_variant E411G 1232A>G ESAD-UK 8 145581697 145581697 single base substitution C T exon_variant ESAD-UK 8 145581697 145581697 single base substitution C T synonymous_variant L137L 411G>A ESAD-UK 8 145581697 145581697 single base substitution C T upstream_gene_variant ESAD-UK 8 145582407 145582407 single base substitution G T exon_variant ESAD-UK 8 145582407 145582407 single base substitution G T upstream_gene_variant ESAD-UK 8 145584126 145584126 single base substitution G T upstream_gene_variant ESAD-UK 8 145585601 145585601 single base substitution T C upstream_gene_variant ESCA-CN 8 145578234 145578234 single base substitution T C downstream_gene_variant ESCA-CN 8 145578238 145578238 single base substitution A C downstream_gene_variant ESCA-CN 8 145578354 145578354 single base substitution A T downstream_gene_variant ESCA-CN 8 145582839 145582839 single base substitution T C exon_variant ESCA-CN 8 145582839 145582839 single base substitution T C upstream_gene_variant ESCA-CN 8 145583536 145583536 single base substitution G A upstream_gene_variant GBM-US 8 145579316 145579316 single base substitution C G downstream_gene_variant GBM-US 8 145579316 145579316 single base substitution C G exon_variant GBM-US 8 145579316 145579316 single base substitution C G missense_variant G493R 1477G>C GBM-US 8 145579316 145579316 single base substitution C G missense_variant G499R 1495G>C GBM-US 8 145581939 145581939 single base substitution G A exon_variant GBM-US 8 145581939 145581939 single base substitution G A missense_variant P57S 169C>T GBM-US 8 145581939 145581939 single base substitution G A upstream_gene_variant KIRC-US 8 145584463 145584463 single base substitution G A upstream_gene_variant KIRC-US 8 145584534 145584534 insertion of <=200bp - G upstream_gene_variant KIRP-US 8 145579793 145579793 single base substitution T C downstream_gene_variant KIRP-US 8 145579793 145579793 single base substitution T C exon_variant KIRP-US 8 145579793 145579793 single base substitution T C intron_variant KIRP-US 8 145579793 145579793 single base substitution T C missense_variant Q430R 1289A>G KIRP-US 8 145579793 145579793 single base substitution T C missense_variant Q436R 1307A>G LAML-KR 8 145579931 145579931 single base substitution C G downstream_gene_variant LAML-KR 8 145579931 145579931 single base substitution C G intron_variant LAML-KR 8 145579932 145579932 single base substitution C T downstream_gene_variant LAML-KR 8 145579932 145579932 single base substitution C T intron_variant LAML-KR 8 145579943 145579943 single base substitution C A downstream_gene_variant LAML-KR 8 145579943 145579943 single base substitution C A intron_variant LAML-KR 8 145579950 145579950 single base substitution G A downstream_gene_variant LAML-KR 8 145579950 145579950 single base substitution G A intron_variant LAML-KR 8 145579953 145579953 single base substitution T A downstream_gene_variant LAML-KR 8 145579953 145579953 single base substitution T A splice_region_variant LAML-KR 8 145579954 145579954 single base substitution G A downstream_gene_variant LAML-KR 8 145579954 145579954 single base substitution G A splice_region_variant LGG-US 8 145580132 145580132 single base substitution G A downstream_gene_variant LGG-US 8 145580132 145580132 single base substitution G A exon_variant LGG-US 8 145580132 145580132 single base substitution G A synonymous_variant P345P 1035C>T LGG-US 8 145580132 145580132 single base substitution G A synonymous_variant P351P 1053C>T LGG-US 8 145583069 145583069 single base substitution A G upstream_gene_variant LGG-US 8 145583729 145583729 single base substitution G A upstream_gene_variant LGG-US 8 145584537 145584537 single base substitution G C upstream_gene_variant LICA-FR 8 145577702 145577702 single base substitution G A downstream_gene_variant LICA-FR 8 145577738 145577738 single base substitution C T downstream_gene_variant LICA-FR 8 145577810 145577810 single base substitution C T downstream_gene_variant LICA-FR 8 145577931 145577931 single base substitution C A downstream_gene_variant LICA-FR 8 145581440 145581440 single base substitution C A exon_variant LICA-FR 8 145581440 145581440 single base substitution C A synonymous_variant A141A 423G>T LICA-FR 8 145581440 145581440 single base substitution C A upstream_gene_variant LICA-FR 8 145581950 145581950 single base substitution C G exon_variant LICA-FR 8 145581950 145581950 single base substitution C G missense_variant G53A 158G>C LICA-FR 8 145581950 145581950 single base substitution C G upstream_gene_variant LICA-FR 8 145582017 145582017 single base substitution C T exon_variant LICA-FR 8 145582017 145582017 single base substitution C T missense_variant A31T 91G>A LICA-FR 8 145582017 145582017 single base substitution C T upstream_gene_variant LICA-FR 8 145585667 145585667 single base substitution G C upstream_gene_variant LIHC-US 8 145579629 145579629 single base substitution T C downstream_gene_variant LIHC-US 8 145579629 145579629 single base substitution T C intron_variant LIHC-US 8 145579629 145579629 single base substitution T C missense_variant S485G 1453A>G LIHC-US 8 145579629 145579629 single base substitution T C missense_variant S491G 1471A>G LIHC-US 8 145579629 145579629 single base substitution T C splice_region_variant LIHC-US 8 145580146 145580146 single base substitution G C downstream_gene_variant LIHC-US 8 145580146 145580146 single base substitution G C exon_variant LIHC-US 8 145580146 145580146 single base substitution G C missense_variant R341G 1021C>G LIHC-US 8 145580146 145580146 single base substitution G C missense_variant R347G 1039C>G LIHC-US 8 145584307 145584307 single base substitution G A upstream_gene_variant LINC-JP 8 145577666 145577666 single base substitution C T downstream_gene_variant LINC-JP 8 145578534 145578543 deletion of <=200bp CAGGAAGGAG - downstream_gene_variant LINC-JP 8 145579936 145579936 single base substitution C T downstream_gene_variant LINC-JP 8 145579936 145579936 single base substitution C T intron_variant LINC-JP 8 145579951 145579951 deletion of <=200bp A - downstream_gene_variant LINC-JP 8 145579951 145579951 deletion of <=200bp A - intron_variant LINC-JP 8 145580654 145580654 single base substitution G C downstream_gene_variant LINC-JP 8 145580654 145580654 single base substitution G C exon_variant LINC-JP 8 145580654 145580654 single base substitution G C missense_variant S250C 749C>G LINC-JP 8 145580654 145580654 single base substitution G C missense_variant S256C 767C>G LINC-JP 8 145580654 145580654 single base substitution G C upstream_gene_variant LINC-JP 8 145584677 145584677 single base substitution C T upstream_gene_variant LIRI-JP 8 145580250 145580250 single base substitution C T downstream_gene_variant LIRI-JP 8 145580250 145580250 single base substitution C T exon_variant LIRI-JP 8 145580250 145580250 single base substitution C T intron_variant LIRI-JP 8 145580557 145580557 single base substitution C A downstream_gene_variant LIRI-JP 8 145580557 145580557 single base substitution C A exon_variant LIRI-JP 8 145580557 145580557 single base substitution C A missense_variant V258L 772G>T LIRI-JP 8 145580557 145580557 single base substitution C A missense_variant V264L 790G>T LIRI-JP 8 145580557 145580557 single base substitution C A upstream_gene_variant LIRI-JP 8 145580812 145580812 single base substitution G T downstream_gene_variant LIRI-JP 8 145580812 145580812 single base substitution G T exon_variant LIRI-JP 8 145580812 145580812 single base substitution G T intron_variant LIRI-JP 8 145580812 145580812 single base substitution G T upstream_gene_variant LIRI-JP 8 145584770 145584770 single base substitution C A upstream_gene_variant LIRI-JP 8 145585149 145585149 single base substitution G A upstream_gene_variant LUSC-KR 8 145574414 145574414 single base substitution G A downstream_gene_variant LUSC-KR 8 145574825 145574825 single base substitution C T downstream_gene_variant LUSC-KR 8 145575931 145575931 single base substitution G T downstream_gene_variant LUSC-KR 8 145577824 145577824 single base substitution C G downstream_gene_variant LUSC-KR 8 145577829 145577829 single base substitution A C downstream_gene_variant LUSC-KR 8 145579931 145579931 single base substitution C G downstream_gene_variant LUSC-KR 8 145579931 145579931 single base substitution C G intron_variant LUSC-KR 8 145579932 145579932 single base substitution C T downstream_gene_variant LUSC-KR 8 145579932 145579932 single base substitution C T intron_variant LUSC-KR 8 145579936 145579936 single base substitution C T downstream_gene_variant LUSC-KR 8 145579936 145579936 single base substitution C T intron_variant LUSC-KR 8 145579943 145579943 single base substitution C A downstream_gene_variant LUSC-KR 8 145579943 145579943 single base substitution C A intron_variant LUSC-KR 8 145579950 145579950 single base substitution G A downstream_gene_variant LUSC-KR 8 145579950 145579950 single base substitution G A intron_variant LUSC-KR 8 145579951 145579951 single base substitution A C downstream_gene_variant LUSC-KR 8 145579951 145579951 single base substitution A C intron_variant LUSC-KR 8 145579953 145579953 single base substitution T A downstream_gene_variant LUSC-KR 8 145579953 145579953 single base substitution T A splice_region_variant LUSC-KR 8 145579954 145579954 single base substitution G A downstream_gene_variant LUSC-KR 8 145579954 145579954 single base substitution G A splice_region_variant LUSC-KR 8 145580984 145580984 single base substitution A G downstream_gene_variant LUSC-KR 8 145580984 145580984 single base substitution A G exon_variant LUSC-KR 8 145580984 145580984 single base substitution A G intron_variant LUSC-KR 8 145580984 145580984 single base substitution A G upstream_gene_variant LUSC-KR 8 145581618 145581618 single base substitution C A exon_variant LUSC-KR 8 145581618 145581618 single base substitution C A intron_variant LUSC-KR 8 145581618 145581618 single base substitution C A upstream_gene_variant LUSC-KR 8 145582504 145582504 single base substitution C T exon_variant LUSC-KR 8 145582504 145582504 single base substitution C T upstream_gene_variant LUSC-KR 8 145582839 145582839 single base substitution T C exon_variant LUSC-KR 8 145582839 145582839 single base substitution T C upstream_gene_variant LUSC-KR 8 145583670 145583670 single base substitution C T upstream_gene_variant LUSC-KR 8 145583707 145583707 single base substitution C T upstream_gene_variant LUSC-US 8 145579815 145579815 single base substitution C T downstream_gene_variant LUSC-US 8 145579815 145579815 single base substitution C T exon_variant LUSC-US 8 145579815 145579815 single base substitution C T intron_variant LUSC-US 8 145579815 145579815 single base substitution C T missense_variant E423K 1267G>A LUSC-US 8 145579815 145579815 single base substitution C T missense_variant E429K 1285G>A LUSC-US 8 145584541 145584541 single base substitution C T upstream_gene_variant LUSC-US 8 145584561 145584561 single base substitution C T upstream_gene_variant MALY-DE 8 145574707 145574707 single base substitution C A downstream_gene_variant MALY-DE 8 145577323 145577323 single base substitution C T downstream_gene_variant MALY-DE 8 145583852 145583852 single base substitution C G upstream_gene_variant MELA-AU 8 145574229 145574229 single base substitution C T downstream_gene_variant MELA-AU 8 145574308 145574308 single base substitution C T downstream_gene_variant MELA-AU 8 145574404 145574404 single base substitution C T downstream_gene_variant MELA-AU 8 145574431 145574431 single base substitution C T downstream_gene_variant MELA-AU 8 145574517 145574518 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 8 145574545 145574545 single base substitution C T downstream_gene_variant MELA-AU 8 145574589 145574589 single base substitution C T downstream_gene_variant MELA-AU 8 145574610 145574610 single base substitution C T downstream_gene_variant MELA-AU 8 145574730 145574730 single base substitution C T downstream_gene_variant MELA-AU 8 145574814 145574814 single base substitution C T downstream_gene_variant MELA-AU 8 145575384 145575384 single base substitution G A downstream_gene_variant MELA-AU 8 145576856 145576856 single base substitution G A downstream_gene_variant MELA-AU 8 145577134 145577134 single base substitution G A downstream_gene_variant MELA-AU 8 145577155 145577156 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 8 145577434 145577434 single base substitution C T downstream_gene_variant MELA-AU 8 145577504 145577504 single base substitution G A downstream_gene_variant MELA-AU 8 145577996 145577996 single base substitution G A downstream_gene_variant MELA-AU 8 145578856 145578856 single base substitution C T downstream_gene_variant MELA-AU 8 145579303 145579303 single base substitution A T downstream_gene_variant MELA-AU 8 145579303 145579303 single base substitution A T exon_variant MELA-AU 8 145579303 145579303 single base substitution A T missense_variant L497H 1490T>A MELA-AU 8 145579303 145579303 single base substitution A T missense_variant L503H 1508T>A MELA-AU 8 145579500 145579500 single base substitution G A downstream_gene_variant MELA-AU 8 145579500 145579500 single base substitution G A intron_variant MELA-AU 8 145580365 145580365 single base substitution G A downstream_gene_variant MELA-AU 8 145580365 145580365 single base substitution G A exon_variant MELA-AU 8 145580365 145580365 single base substitution G A synonymous_variant C290C 870C>T MELA-AU 8 145580365 145580365 single base substitution G A synonymous_variant C296C 888C>T MELA-AU 8 145580483 145580483 single base substitution G A downstream_gene_variant MELA-AU 8 145580483 145580483 single base substitution G A exon_variant MELA-AU 8 145580483 145580483 single base substitution G A synonymous_variant I282I 846C>T MELA-AU 8 145580483 145580483 single base substitution G A synonymous_variant I288I 864C>T MELA-AU 8 145581121 145581121 single base substitution G A exon_variant MELA-AU 8 145581121 145581121 single base substitution G A missense_variant S206F 617C>T MELA-AU 8 145581121 145581121 single base substitution G A upstream_gene_variant MELA-AU 8 145581179 145581179 single base substitution G A exon_variant MELA-AU 8 145581179 145581179 single base substitution G A intron_variant MELA-AU 8 145581179 145581179 single base substitution G A upstream_gene_variant MELA-AU 8 145582200 145582201 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 8 145582200 145582201 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 8 145582214 145582214 single base substitution C T exon_variant MELA-AU 8 145582214 145582214 single base substitution C T upstream_gene_variant MELA-AU 8 145582222 145582222 single base substitution G A exon_variant MELA-AU 8 145582222 145582222 single base substitution G A upstream_gene_variant MELA-AU 8 145582223 145582223 single base substitution G A exon_variant MELA-AU 8 145582223 145582223 single base substitution G A upstream_gene_variant MELA-AU 8 145582228 145582228 single base substitution C T exon_variant MELA-AU 8 145582228 145582228 single base substitution C T upstream_gene_variant MELA-AU 8 145582259 145582259 single base substitution G A exon_variant MELA-AU 8 145582259 145582259 single base substitution G A upstream_gene_variant MELA-AU 8 145582641 145582641 single base substitution C T exon_variant MELA-AU 8 145582641 145582641 single base substitution C T upstream_gene_variant MELA-AU 8 145583119 145583119 single base substitution C T upstream_gene_variant MELA-AU 8 145583234 145583234 single base substitution C T upstream_gene_variant MELA-AU 8 145584054 145584054 single base substitution C T upstream_gene_variant MELA-AU 8 145584174 145584174 single base substitution C T upstream_gene_variant MELA-AU 8 145584252 145584252 single base substitution C T upstream_gene_variant MELA-AU 8 145584368 145584368 single base substitution C T upstream_gene_variant MELA-AU 8 145584370 145584370 single base substitution C T upstream_gene_variant MELA-AU 8 145584609 145584609 single base substitution C T upstream_gene_variant MELA-AU 8 145584628 145584628 single base substitution C T upstream_gene_variant MELA-AU 8 145585149 145585149 single base substitution G A upstream_gene_variant MELA-AU 8 145585794 145585794 single base substitution C T upstream_gene_variant MELA-AU 8 145586167 145586167 single base substitution C T upstream_gene_variant MELA-AU 8 145586327 145586327 single base substitution G A upstream_gene_variant MELA-AU 8 145586623 145586623 single base substitution C T upstream_gene_variant MELA-AU 8 145587211 145587211 single base substitution C T upstream_gene_variant MELA-AU 8 145587593 145587593 single base substitution C T upstream_gene_variant MELA-AU 8 145587677 145587677 single base substitution G A upstream_gene_variant MELA-AU 8 145587683 145587683 single base substitution C T upstream_gene_variant ORCA-IN 8 145577164 145577164 single base substitution G A downstream_gene_variant ORCA-IN 8 145577727 145577727 single base substitution C T downstream_gene_variant ORCA-IN 8 145583789 145583789 single base substitution G T upstream_gene_variant OV-AU 8 145580381 145580381 single base substitution G C downstream_gene_variant OV-AU 8 145580381 145580381 single base substitution G C splice_region_variant OV-AU 8 145583223 145583223 single base substitution T G upstream_gene_variant OV-AU 8 145583660 145583660 single base substitution C T upstream_gene_variant OV-AU 8 145584337 145584337 single base substitution G A upstream_gene_variant OV-AU 8 145584343 145584343 single base substitution G C upstream_gene_variant OV-AU 8 145584404 145584404 single base substitution G A upstream_gene_variant PACA-CA 8 145577724 145577724 single base substitution C T downstream_gene_variant PACA-CA 8 145581198 145581198 single base substitution T C exon_variant PACA-CA 8 145581198 145581198 single base substitution T C intron_variant PACA-CA 8 145581198 145581198 single base substitution T C upstream_gene_variant PACA-CA 8 145582839 145582839 single base substitution T C exon_variant PACA-CA 8 145582839 145582839 single base substitution T C upstream_gene_variant PACA-CA 8 145587754 145587754 single base substitution G A upstream_gene_variant PAEN-IT 8 145579286 145579286 single base substitution G A downstream_gene_variant PAEN-IT 8 145579286 145579286 single base substitution G A exon_variant PAEN-IT 8 145579286 145579286 single base substitution G A missense_variant R503C 1507C>T PAEN-IT 8 145579286 145579286 single base substitution G A missense_variant R509C 1525C>T PRAD-CA 8 145578029 145578029 single base substitution G T downstream_gene_variant PRAD-US 8 145579796 145579796 single base substitution G T downstream_gene_variant PRAD-US 8 145579796 145579796 single base substitution G T exon_variant PRAD-US 8 145579796 145579796 single base substitution G T intron_variant PRAD-US 8 145579796 145579796 single base substitution G T missense_variant T429N 1286C>A PRAD-US 8 145579796 145579796 single base substitution G T missense_variant T435N 1304C>A PRAD-US 8 145583505 145583505 single base substitution C A upstream_gene_variant READ-US 8 145580529 145580529 single base substitution C T downstream_gene_variant READ-US 8 145580529 145580529 single base substitution C T exon_variant READ-US 8 145580529 145580529 single base substitution C T missense_variant R267Q 800G>A READ-US 8 145580529 145580529 single base substitution C T missense_variant R273Q 818G>A READ-US 8 145580529 145580529 single base substitution C T upstream_gene_variant READ-US 8 145583598 145583598 single base substitution T C upstream_gene_variant RECA-EU 8 145585588 145585588 single base substitution C T upstream_gene_variant SKCA-BR 8 145574361 145574361 single base substitution C T downstream_gene_variant SKCA-BR 8 145574468 145574468 single base substitution T C downstream_gene_variant SKCA-BR 8 145574930 145574930 single base substitution A G downstream_gene_variant SKCA-BR 8 145577731 145577731 single base substitution G A downstream_gene_variant SKCA-BR 8 145578851 145578851 single base substitution A C downstream_gene_variant SKCA-BR 8 145578857 145578857 single base substitution T C downstream_gene_variant SKCA-BR 8 145578861 145578861 single base substitution A C downstream_gene_variant SKCA-BR 8 145582228 145582228 single base substitution C T exon_variant SKCA-BR 8 145582228 145582228 single base substitution C T upstream_gene_variant SKCA-BR 8 145582229 145582229 single base substitution C T exon_variant SKCA-BR 8 145582229 145582229 single base substitution C T upstream_gene_variant SKCA-BR 8 145582236 145582236 single base substitution G A exon_variant SKCA-BR 8 145582236 145582236 single base substitution G A upstream_gene_variant SKCA-BR 8 145582237 145582237 single base substitution G A exon_variant SKCA-BR 8 145582237 145582237 single base substitution G A upstream_gene_variant SKCA-BR 8 145584914 145584914 single base substitution A T upstream_gene_variant SKCA-BR 8 145586073 145586073 single base substitution C T upstream_gene_variant SKCM-US 8 145579332 145579333 deletion of <=200bp CA - downstream_gene_variant SKCM-US 8 145579332 145579333 deletion of <=200bp CA - exon_variant SKCM-US 8 145579332 145579333 deletion of <=200bp CA - frameshift_variant V487 SKCM-US 8 145579332 145579333 deletion of <=200bp CA - frameshift_variant V493 SKCM-US 8 145579670 145579670 single base substitution G A downstream_gene_variant SKCM-US 8 145579670 145579670 single base substitution G A exon_variant SKCM-US 8 145579670 145579670 single base substitution G A intron_variant SKCM-US 8 145579670 145579670 single base substitution G A missense_variant S471F 1412C>T SKCM-US 8 145579670 145579670 single base substitution G A missense_variant S477F 1430C>T SKCM-US 8 145579751 145579751 single base substitution T G downstream_gene_variant SKCM-US 8 145579751 145579751 single base substitution T G exon_variant SKCM-US 8 145579751 145579751 single base substitution T G intron_variant SKCM-US 8 145579751 145579751 single base substitution T G missense_variant Q444P 1331A>C SKCM-US 8 145579751 145579751 single base substitution T G missense_variant Q450P 1349A>C SKCM-US 8 145579875 145579875 single base substitution C T downstream_gene_variant SKCM-US 8 145579875 145579875 single base substitution C T intron_variant SKCM-US 8 145579875 145579875 single base substitution C T splice_acceptor_variant SKCM-US 8 145580011 145580011 single base substitution G A downstream_gene_variant SKCM-US 8 145580011 145580011 single base substitution G A exon_variant SKCM-US 8 145580011 145580011 single base substitution G A missense_variant R386C 1156C>T SKCM-US 8 145580011 145580011 single base substitution G A missense_variant R392C 1174C>T SKCM-US 8 145580114 145580114 single base substitution G A downstream_gene_variant SKCM-US 8 145580114 145580114 single base substitution G A exon_variant SKCM-US 8 145580114 145580114 single base substitution G A synonymous_variant S351S 1053C>T SKCM-US 8 145580114 145580114 single base substitution G A synonymous_variant S357S 1071C>T SKCM-US 8 145580326 145580326 single base substitution G A downstream_gene_variant SKCM-US 8 145580326 145580326 single base substitution G A exon_variant SKCM-US 8 145580326 145580326 single base substitution G A synonymous_variant I303I 909C>T SKCM-US 8 145580326 145580326 single base substitution G A synonymous_variant I309I 927C>T SKCM-US 8 145583069 145583069 single base substitution A G upstream_gene_variant SKCM-US 8 145583581 145583581 single base substitution C T upstream_gene_variant SKCM-US 8 145583638 145583638 single base substitution C T upstream_gene_variant SKCM-US 8 145583659 145583659 single base substitution C T upstream_gene_variant SKCM-US 8 145583669 145583669 single base substitution C T upstream_gene_variant SKCM-US 8 145583692 145583692 single base substitution C T upstream_gene_variant SKCM-US 8 145583942 145583942 single base substitution C T upstream_gene_variant SKCM-US 8 145583947 145583947 single base substitution C T upstream_gene_variant SKCM-US 8 145584116 145584116 single base substitution C T upstream_gene_variant SKCM-US 8 145584131 145584131 single base substitution C T upstream_gene_variant SKCM-US 8 145584592 145584592 single base substitution G T upstream_gene_variant STAD-US 8 145579191 145579191 single base substitution C A downstream_gene_variant STAD-US 8 145579191 145579191 single base substitution C A exon_variant STAD-US 8 145579191 145579191 single base substitution C A stop_lost *534Y 1602G>T STAD-US 8 145579191 145579191 single base substitution C A stop_lost *540Y 1620G>T STAD-US 8 145579255 145579255 single base substitution T C downstream_gene_variant STAD-US 8 145579255 145579255 single base substitution T C exon_variant STAD-US 8 145579255 145579255 single base substitution T C missense_variant Y513C 1538A>G STAD-US 8 145579255 145579255 single base substitution T C missense_variant Y519C 1556A>G STAD-US 8 145579642 145579642 single base substitution T C downstream_gene_variant STAD-US 8 145579642 145579642 single base substitution T C exon_variant STAD-US 8 145579642 145579642 single base substitution T C intron_variant STAD-US 8 145579642 145579642 single base substitution T C synonymous_variant T480T 1440A>G STAD-US 8 145579642 145579642 single base substitution T C synonymous_variant T486T 1458A>G STAD-US 8 145579704 145579704 single base substitution T C downstream_gene_variant STAD-US 8 145579704 145579704 single base substitution T C exon_variant STAD-US 8 145579704 145579704 single base substitution T C intron_variant STAD-US 8 145579704 145579704 single base substitution T C missense_variant S460G 1378A>G STAD-US 8 145579704 145579704 single base substitution T C missense_variant S466G 1396A>G STAD-US 8 145579803 145579803 single base substitution A G downstream_gene_variant STAD-US 8 145579803 145579803 single base substitution A G exon_variant STAD-US 8 145579803 145579803 single base substitution A G intron_variant STAD-US 8 145579803 145579803 single base substitution A G missense_variant F427L 1279T>C STAD-US 8 145579803 145579803 single base substitution A G missense_variant F433L 1297T>C STAD-US 8 145580025 145580025 single base substitution C T downstream_gene_variant STAD-US 8 145580025 145580025 single base substitution C T exon_variant STAD-US 8 145580025 145580025 single base substitution C T missense_variant R381H 1142G>A STAD-US 8 145580025 145580025 single base substitution C T missense_variant R387H 1160G>A STAD-US 8 145580161 145580161 single base substitution G A downstream_gene_variant STAD-US 8 145580161 145580161 single base substitution G A exon_variant STAD-US 8 145580161 145580161 single base substitution G A missense_variant P336S 1006C>T STAD-US 8 145580161 145580161 single base substitution G A missense_variant P342S 1024C>T STAD-US 8 145580194 145580194 deletion of <=200bp G - downstream_gene_variant STAD-US 8 145580194 145580194 deletion of <=200bp G - exon_variant STAD-US 8 145580194 145580194 deletion of <=200bp G - splice_region_variant STAD-US 8 145580725 145580725 single base substitution A G downstream_gene_variant STAD-US 8 145580725 145580725 single base substitution A G exon_variant STAD-US 8 145580725 145580725 single base substitution A G synonymous_variant G226G 678T>C STAD-US 8 145580725 145580725 single base substitution A G synonymous_variant G232G 696T>C STAD-US 8 145580725 145580725 single base substitution A G upstream_gene_variant STAD-US 8 145582977 145582977 single base substitution T C intron_variant STAD-US 8 145582977 145582977 single base substitution T C upstream_gene_variant STAD-US 8 145583308 145583308 single base substitution T C upstream_gene_variant STAD-US 8 145583577 145583577 single base substitution G A upstream_gene_variant STAD-US 8 145583653 145583653 single base substitution G T upstream_gene_variant STAD-US 8 145583729 145583729 single base substitution G A upstream_gene_variant STAD-US 8 145583773 145583773 single base substitution A G upstream_gene_variant STAD-US 8 145583901 145583901 single base substitution T C upstream_gene_variant STAD-US 8 145584371 145584371 single base substitution G A upstream_gene_variant STAD-US 8 145584466 145584466 single base substitution C A upstream_gene_variant UCEC-US 8 145579318 145579318 single base substitution G A downstream_gene_variant UCEC-US 8 145579318 145579318 single base substitution G A exon_variant UCEC-US 8 145579318 145579318 single base substitution G A missense_variant P492L 1475C>T UCEC-US 8 145579318 145579318 single base substitution G A missense_variant P498L 1493C>T UCEC-US 8 145579713 145579713 single base substitution C T downstream_gene_variant UCEC-US 8 145579713 145579713 single base substitution C T exon_variant UCEC-US 8 145579713 145579713 single base substitution C T intron_variant UCEC-US 8 145579713 145579713 single base substitution C T missense_variant A457T 1369G>A UCEC-US 8 145579713 145579713 single base substitution C T missense_variant A463T 1387G>A UCEC-US 8 145580053 145580053 single base substitution G T downstream_gene_variant UCEC-US 8 145580053 145580053 single base substitution G T exon_variant UCEC-US 8 145580053 145580053 single base substitution G T missense_variant R372S 1114C>A UCEC-US 8 145580053 145580053 single base substitution G T missense_variant R378S 1132C>A UCEC-US 8 145580524 145580524 single base substitution G A downstream_gene_variant UCEC-US 8 145580524 145580524 single base substitution G A exon_variant UCEC-US 8 145580524 145580524 single base substitution G A missense_variant R269C 805C>T UCEC-US 8 145580524 145580524 single base substitution G A missense_variant R275C 823C>T UCEC-US 8 145580524 145580524 single base substitution G A upstream_gene_variant UCEC-US 8 145580713 145580713 single base substitution G A downstream_gene_variant UCEC-US 8 145580713 145580713 single base substitution G A exon_variant UCEC-US 8 145580713 145580713 single base substitution G A synonymous_variant D230D 690C>T UCEC-US 8 145580713 145580713 single base substitution G A synonymous_variant D236D 708C>T UCEC-US 8 145580713 145580713 single base substitution G A upstream_gene_variant UCEC-US 8 145580740 145580740 single base substitution G T downstream_gene_variant UCEC-US 8 145580740 145580740 single base substitution G T exon_variant UCEC-US 8 145580740 145580740 single base substitution G T synonymous_variant L221L 663C>A UCEC-US 8 145580740 145580740 single base substitution G T synonymous_variant L227L 681C>A UCEC-US 8 145580740 145580740 single base substitution G T upstream_gene_variant UCEC-US 8 145583536 145583536 single base substitution G A upstream_gene_variant UCEC-US 8 145583655 145583655 single base substitution G A upstream_gene_variant UCEC-US 8 145583921 145583921 single base substitution G A upstream_gene_variant UCEC-US 8 145584581 145584581 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand sysucc-882T COSM5426545 c.1225+6C>T p.? Unknown 8:144356294-144356294 - 587350 COSM1206785 c.1256G>A p.G419D Substitution - Missense 8:144356184-144356184 - TCGA-BF-A1Q0-01 COSM3646568 c.927C>T p.I309I Substitution - coding silent 8:144356666-144356666 - LIM1215 COSM4366280 c.957T>C p.P319P Substitution - coding silent 8:144356636-144356636 - TCGA-A6-6651-01 COSM1455611 c.1223G>A p.R408Q Substitution - Missense 8:144356302-144356302 - PTC-73C COSM1455611 c.1223G>A p.R408Q Substitution - Missense 8:144356302-144356302 - GC_361T-GC_361N COSM4774783 c.1046T>G p.V349G Substitution - Missense 8:144356479-144356479 - C32 COSM4619319 c.1196C>T p.P399L Substitution - Missense 8:144356329-144356329 - LC_C23 COSM1190808 c.613delA p.K205fs*8 Deletion - Frameshift 8:144357465-144357465 - CSCC-49-T COSM4495580 c.456C>T p.S152S Substitution - coding silent 8:144357747-144357747 - PD9592a COSM5782457 c.676A>G p.K226E Substitution - Missense 8:144357085-144357085 - S02065 COSM5672962 c.693C>T p.H231H Substitution - coding silent 8:144357068-144357068 - sysucc-1116T COSM5426545 c.1225+6C>T p.? Unknown 8:144356294-144356294 - TCGA-FV-A23B-01 COSM4914295 c.1471A>G p.S491G Substitution - Missense 8:144355969-144355969 - 259 COSM3732562 c.1039C>T p.R347* Substitution - Nonsense 8:144356486-144356486 - sysucc-882T COSM5426546 c.1225+7A>T p.? Unknown 8:144356293-144356293 - S02065 COSM2871161 c.709G>A p.A237T Substitution - Missense 8:144357052-144357052 - TCGA-D5-6927-01 COSM3686372 c.772-3delC p.? Unknown 8:144356918-144356918 - CSCC-4-T COSM4448980 c.1537delC p.R513fs*3 Deletion - Frameshift 8:144355614-144355614 - TCGA-BR-4361-01 COSM3898184 c.1458A>G p.T486T Substitution - coding silent 8:144355982-144355982 - PTC-88C COSM1455612 c.1221T>C p.C407C Substitution - coding silent 8:144356304-144356304 - TCGA-EE-A3JD-06 COSM4397418 c.1430C>T p.S477F Substitution - Missense 8:144356010-144356010 - TCGA-B5-A11Y-01 COSM1097204 c.1493C>T p.P498L Substitution - Missense 8:144355658-144355658 - CHC1750T COSM4792634 c.423G>T p.A141A Substitution - coding silent 8:144357780-144357780 - LN229 COSM1455612 c.1221T>C p.C407C Substitution - coding silent 8:144356304-144356304 - TCGA-18-3409-01 COSM749625 c.1285G>A p.E429K Substitution - Missense 8:144356155-144356155 - 112509 COSM94278 c.1317C>G p.C439W Substitution - Missense 8:144356123-144356123 - SNUH_G16_S1 COSM3685349 c.1259C>G p.T420R Substitution - Missense 8:144356181-144356181 - sysucc-1116T COSM5426546 c.1225+7A>T p.? Unknown 8:144356293-144356293 - CN-AML-CR-19-Dx COSM5426570 c.1225+10C>T p.? Unknown 8:144356290-144356290 - sysucc-679T COSM5426570 c.1225+10C>T p.? Unknown 8:144356290-144356290 - CHC1725T COSM4800641 c.158G>C p.G53A Substitution - Missense 8:144358290-144358290 - TCGA-BH-A18G-01 COSM3732562 c.1039C>T p.R347* Substitution - Nonsense 8:144356486-144356486 - sysucc-1116T COSM5426570 c.1225+10C>T p.? Unknown 8:144356290-144356290 - PD5960a COSM5778571 c.1372G>T p.E458* Substitution - Nonsense 8:144356068-144356068 - T3064 COSM4683895 c.1352G>T p.G451V Substitution - Missense 8:144356088-144356088 - PT08_2 COSM5893297 c.1120G>A p.E374K Substitution - Missense 8:144356405-144356405 - 2492721 COSM5721286 c.859G>A p.A287T Substitution - Missense 8:144356828-144356828 - PTC-73C COSM1455613 c.1218A>G p.P406P Substitution - coding silent 8:144356307-144356307 - CHC432T COSM4800641 c.158G>C p.G53A Substitution - Missense 8:144358290-144358290 - CN-AML-CR-19-Dx COSM5426546 c.1225+7A>T p.? Unknown 8:144356293-144356293 - CRC-01T COSM5426570 c.1225+10C>T p.? Unknown 8:144356290-144356290 - PTC-53C COSM1455612 c.1221T>C p.C407C Substitution - coding silent 8:144356304-144356304 - TCGA-32-1977-01 COSM3412854 c.1495G>C p.G499R Substitution - Missense 8:144355656-144355656 - 938T COSM5825168 c.1525C>T p.R509C Substitution - Missense 8:144355626-144355626 - T3225 COSM4683894 c.1505A>G p.Y502C Substitution - Missense 8:144355646-144355646 - CHC1750T COSM4792634 c.423G>T p.A141A Substitution - coding silent 8:144357780-144357780 - TCGA-D1-A176-01 COSM1097208 c.708C>T p.D236D Substitution - coding silent 8:144357053-144357053 - pfg008T COSM1643549 c.1354T>A p.F452I Substitution - Missense 8:144356086-144356086 - XHDG40 COSM4770070 c.569C>A p.P190H Substitution - Missense 8:144357634-144357634 - TCGA-HU-A4G8-01 COSM3898186 c.1160G>A p.R387H Substitution - Missense 8:144356365-144356365 - CHC327T COSM4950589 c.91G>A p.A31T Substitution - Missense 8:144358357-144358357 - I2L-P19Ta-Tumor-Organoid COSM5358716 c.271G>C p.A91P Substitution - Missense 8:144358177-144358177 - TCGA-FS-A1ZK-06 COSM3646564 c.1349A>C p.Q450P Substitution - Missense 8:144356091-144356091 - TCGA-BT-A2LB-01 COSM3779081 c.1072C>T p.L358L Substitution - coding silent 8:144356453-144356453 - TCGA-DA-A1IA-06 COSM3646565 c.1226-1G>A p.? Unknown 8:144356215-144356215 - TCGA-B5-A11E-01 COSM1097209 c.681C>A p.L227L Substitution - coding silent 8:144357080-144357080 - ESO-161 COSM1252245 c.1A>G p.M1V Substitution - Missense 8:144358447-144358447 - LS180 COSM4646205 c.9C>T p.A3A Substitution - coding silent 8:144358439-144358439 - TCGA-F4-6856-01 COSM1455614 c.834G>A p.W278* Substitution - Nonsense 8:144356853-144356853 - PTC-53C COSM1455613 c.1218A>G p.P406P Substitution - coding silent 8:144356307-144356307 - PTC-53C COSM1455611 c.1223G>A p.R408Q Substitution - Missense 8:144356302-144356302 - 66 COSM5743310 c.1202G>A p.G401D Substitution - Missense 8:144356323-144356323 - 8066081 COSM3785909 c.109T>G p.Y37D Substitution - Missense 8:144358339-144358339 - TCGA-D5-6930-01 COSM1455610 c.1317C>T p.C439C Substitution - coding silent 8:144356123-144356123 - PTC-50C COSM1455613 c.1218A>G p.P406P Substitution - coding silent 8:144356307-144356307 - sysucc-882T COSM5426570 c.1225+10C>T p.? Unknown 8:144356290-144356290 - TCGA-BR-4362-01 COSM2871142 c.1396A>G p.S466G Substitution - Missense 8:144356044-144356044 - TCGA-P5-A5EW-01 COSM3929457 c.1053C>T p.P351P Substitution - coding silent 8:144356472-144356472 - CHC432T COSM4800641 c.158G>C p.G53A Substitution - Missense 8:144358290-144358290 - 2492720 COSM5721286 c.859G>A p.A287T Substitution - Missense 8:144356828-144356828 - ESCC_72 COSM5634418 c.1186C>T p.R396C Substitution - Missense 8:144356339-144356339 - TCGA-EE-A3J5-06 COSM3646567 c.1071C>T p.S357S Substitution - coding silent 8:144356454-144356454 - PTC-73C COSM1455612 c.1221T>C p.C407C Substitution - coding silent 8:144356304-144356304 - T2197 COSM4683897 c.994-2delA p.? Unknown 8:144356533-144356533 - CHC327T COSM4950589 c.91G>A p.A31T Substitution - Missense 8:144358357-144358357 - TCGA-B5-A11E-01 COSM1097205 c.1387G>A p.A463T Substitution - Missense 8:144356053-144356053 - SNU-C4 COSM4615813 c.1301delT p.L434fs*1 Deletion - Frameshift 8:144356139-144356139 - PTC-50C COSM1455612 c.1221T>C p.C407C Substitution - coding silent 8:144356304-144356304 - C086 COSM5531100 c.745C>T p.H249Y Substitution - Missense 8:144357016-144357016 - RK164_C01 COSM3703375 c.790G>T p.V264L Substitution - Missense 8:144356897-144356897 - 139 COSM3721794 c.1146C>T p.G382G Substitution - coding silent 8:144356379-144356379 - TCGA-EE-A3J5-06 COSM3646566 c.1174C>T p.R392C Substitution - Missense 8:144356351-144356351 - TCGA-A7-A26J-01 COSM3834275 c.751C>A p.L251M Substitution - Missense 8:144357010-144357010 - LS174T COSM4646205 c.9C>T p.A3A Substitution - coding silent 8:144358439-144358439 - TCGA-AP-A059-01 COSM1097206 c.1132C>A p.R378S Substitution - Missense 8:144356393-144356393 - TCGA-BR-4257-01 COSM3898188 c.696T>C p.G232G Substitution - coding silent 8:144357065-144357065 - RK308_C01 COSM3768746 c.993+10G>A p.? Unknown 8:144356590-144356590 - TCGA-EI-6917-01 COSM3432211 c.818G>A p.R273Q Substitution - Missense 8:144356869-144356869 - CN-AML-CR-19-Dx COSM5426545 c.1225+6C>T p.? Unknown 8:144356294-144356294 - LIM2405 COSM4613752 c.1403_1404insC p.G469fs*11 Insertion - Frameshift 8:144356036-144356037 - sysucc-731T COSM5426570 c.1225+10C>T p.? Unknown 8:144356290-144356290 - LN229 COSM1455613 c.1218A>G p.P406P Substitution - coding silent 8:144356307-144356307 - T3262 COSM4683896 c.1188C>T p.R396R Substitution - coding silent 8:144356337-144356337 - TCGA-HU-A4GT-01 COSM3898185 c.1297T>C p.F433L Substitution - Missense 8:144356143-144356143 - 2492723 COSM5721286 c.859G>A p.A287T Substitution - Missense 8:144356828-144356828 - LN229 COSM1455611 c.1223G>A p.R408Q Substitution - Missense 8:144356302-144356302 - sysucc-761T COSM5426545 c.1225+6C>T p.? Unknown 8:144356294-144356294 - TCGA-CG-5721-01 COSM3898183 c.1556A>G p.Y519C Substitution - Missense 8:144355595-144355595 - PT38 COSM5943820 c.1225+7delA p.? Unknown 8:144356293-144356293 - S02285 COSM5685015 c.1550G>T p.R517L Substitution - Missense 8:144355601-144355601 - TCGA-26-1439-01 COSM3412855 c.169C>T p.P57S Substitution - Missense 8:144358279-144358279 - TCGA-AA-3713-01 COSM1455611 c.1223G>A p.R408Q Substitution - Missense 8:144356302-144356302 - sysucc-679T COSM5426545 c.1225+6C>T p.? Unknown 8:144356294-144356294 - TCGA-BR-4362-01 COSM3898187 c.1024C>T p.P342S Substitution - Missense 8:144356501-144356501 - PTC-88C COSM1455611 c.1223G>A p.R408Q Substitution - Missense 8:144356302-144356302 - HX34T COSM3663650 c.767C>G p.S256C Substitution - Missense 8:144356994-144356994 - LC_C23 COSM1191130 c.612delG p.W204fs*1 Deletion - Frameshift 8:144357466-144357466 - TCGA-F4-6570-01 COSM1455609 c.1327C>T p.R443* Substitution - Nonsense 8:144356113-144356113 - PTC-50C COSM1455611 c.1223G>A p.R408Q Substitution - Missense 8:144356302-144356302 - LUAD-F00162 COSM366712 c.575G>T p.R192L Substitution - Missense 8:144357628-144357628 - CSCC-27-T COSM4457914 c.1065C>T p.F355F Substitution - coding silent 8:144356460-144356460 - ESCC_21 COSM5626328 c.55C>T p.P19S Substitution - Missense 8:144358393-144358393 - SS6003133 COSM3665321 c.1558C>T p.R520W Substitution - Missense 8:144355593-144355593 - PT08_1 COSM5893297 c.1120G>A p.E374K Substitution - Missense 8:144356405-144356405 - SNUH_G26_S1 COSM3685350 c.1225+7A>C p.? Unknown 8:144356293-144356293 - TCGA-HU-A4GT-01 COSM3898182 c.1620G>T p.*540Y Nonstop extension 8:144355531-144355531 - 104875 COSM94279 c.1091C>T p.A364V Substitution - Missense 8:144356434-144356434 - AOCS-091-1-3 COSM4150657 c.880-8C>G p.? Unknown 8:144356721-144356721 - pfg008T COSM1643549 c.1354T>A p.F452I Substitution - Missense 8:144356086-144356086 - TCGA-G3-A3CH-01 COSM4917994 c.1039C>G p.R347G Substitution - Missense 8:144356486-144356486 - 2492722 COSM5721286 c.859G>A p.A287T Substitution - Missense 8:144356828-144356828 - sysucc-731T COSM5426545 c.1225+6C>T p.? Unknown 8:144356294-144356294 - TCGA-G7-6796-01 COSM3995947 c.1307A>G p.Q436R Substitution - Missense 8:144356133-144356133 - CHC1725T COSM4800641 c.158G>C p.G53A Substitution - Missense 8:144358290-144358290 - A673 COSM4587919 c.1211A>G p.D404G Substitution - Missense 8:144356314-144356314 - T3091 COSM4615813 c.1301delT p.L434fs*1 Deletion - Frameshift 8:144356139-144356139 - TCGA-AP-A0LM-01 COSM1097207 c.823C>T p.R275C Substitution - Missense 8:144356864-144356864 - I2L-P19Ta-Tumor-Biopsy COSM5358716 c.271G>C p.A91P Substitution - Missense 8:144358177-144358177 - TCGA-FD-A3N5-01 COSM1313854 c.1306C>A p.Q436K Substitution - Missense 8:144356134-144356134 - Pat_41_B COSM5874197 c.772-1G>A p.? Unknown 8:144356916-144356916 - TCGA-J4-A67L-01 COSM4391928 c.1304C>A p.T435N Substitution - Missense 8:144356136-144356136 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.12257;Hs.12264;Hs.12271 8q24.3 609076 2481128|CGAP|BC033066|C/T|coding|Leu515Leu|1607|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Synonymous p.G232G c.696T>C 8 145580725 STAD A T Missense p.F452I c.1354T>A 8 145579746 STAD CA - Frameshift p.V493Dfs*102 c.1478_1479delTG 8 145579332 CM C A Missense p.G174W c.520G>T 8 145581343 STAD C G Missense p.G499R c.1495G>C 8 145579316 GBM C T IntronicSNV . c.416+96G>A 8 145581596 CM C T Missense p.R484Q c.1451G>A 8 145579649 HNSC C T SpliceAcceptorSNV . c.1226-1G>A 8 145579875 CM G A Missense p.P498L c.1493C>T 8 145579318 UCEC G A Missense p.P57S c.169C>T 8 145581939 GBM G A Missense p.R392C c.1174C>T 8 145580011 CM G A Missense p.S477F c.1430C>T 8 145579670 CM G A Synonymous p.D236D c.708C>T 8 145580713 UCEC G A Synonymous p.G168G c.504C>T 8 145581359 LUAD G A Synonymous p.L358L c.1072C>T 8 145580113 BLCA G A Synonymous p.S357S c.1071C>T 8 145580114 CM G C Nonsense p.S471* c.1412C>G 8 145579688 CM - G Frameshift p.H38Pfs*180 c.112dupC 8 145581996 STAD GGGGCAGCAGCTGCCCTGCAGA - SpliceAcceptorDeletion . c.880-7_894delTCTGCAGGGCAGCTGCTGCCCC 8 145580359 BRCA G T Missense p.Q436K c.1306C>A 8 145579794 BLCA G T Missense p.T435N c.1304C>A 8 145579796 PRAD T C CdsStartSNV . c.1A>G 8 145582107 ESCA T G Missense p.Q450P c.1349A>C 8 145579751 CM