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 ACC 19 59028363 59028363 + Silent SNP G G A TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr19:59028363G>A c.678C>T c.(676-678)ggC>ggT p.G226G ACC 19 59028585 59028585 + Silent SNP G G A TCGA-OR-A5JR-01A-11D-A29I-10 TCGA-OR-A5JR-10A-01D-A29L-10 g.chr19:59028585G>A c.456C>T c.(454-456)cgC>cgT p.R152R ACC 19 59028585 59028585 + Silent SNP G G A TCGA-OR-A5L9-01A-11D-A29I-10 TCGA-OR-A5L9-10B-01D-A29L-10 g.chr19:59028585G>A c.456C>T c.(454-456)cgC>cgT p.R152R BLCA 19 59025453 59025453 + Missense_Mutation SNP C C G TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr19:59025453C>G c.1504G>C c.(1504-1506)Gag>Cag p.E502Q BLCA 19 59025507 59025507 + Missense_Mutation SNP C C T TCGA-FD-A3B4-01A-12D-A202-08 TCGA-FD-A3B4-10A-01D-A202-08 g.chr19:59025507C>T c.1450G>A c.(1450-1452)Gag>Aag p.E484K BLCA 19 59025544 59025544 + Silent SNP C C T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr19:59025544C>T c.1413G>A c.(1411-1413)aaG>aaA p.K471K BLCA 19 59027763 59027763 + Splice_Site SNP C C T TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr19:59027763C>T c.1278G>A c.(1276-1278)tcG>tcA p.S426S BLCA 19 59027768 59027768 + Missense_Mutation SNP G G A TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr19:59027768G>A c.1273C>T c.(1273-1275)Cac>Tac p.H425Y BLCA 19 59028353 59028353 + Missense_Mutation SNP C C T TCGA-DK-A1AB-01A-11D-A13W-08 TCGA-DK-A1AB-10A-01D-A13W-08 g.chr19:59028353C>T c.688G>A c.(688-690)Gag>Aag p.E230K BLCA 19 59028486 59028486 + Silent SNP T T C TCGA-DK-A3IL-01A-11D-A20D-08 TCGA-DK-A3IL-10A-01D-A20D-08 g.chr19:59028486T>C c.555A>G c.(553-555)ccA>ccG p.P185P BLCA 19 59028629 59028629 + Missense_Mutation SNP T T G TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr19:59028629T>G c.412A>C c.(412-414)Acc>Ccc p.T138P BLCA 19 59028839 59028839 + Nonsense_Mutation SNP C C A TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr19:59028839C>A c.202G>T c.(202-204)Gag>Tag p.E68* BLCA 19 59028913 59028913 + Missense_Mutation SNP G G A TCGA-ZF-A9R9-01A-11D-A38G-08 TCGA-ZF-A9R9-10A-01D-A38J-08 g.chr19:59028913G>A c.128C>T c.(127-129)tCg>tTg p.S43L BRCA 19 59028713 59028713 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr19:59028713G>A c.328C>T c.(328-330)Cgc>Tgc p.R110C CESC 19 59025616 59025616 + Silent SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr19:59025616G>C c.1341C>G c.(1339-1341)ctC>ctG p.L447L CESC 19 59027764 59027764 + Missense_Mutation SNP G G A TCGA-IR-A3LB-01A-11D-A243-09 TCGA-IR-A3LB-10A-01D-A243-09 g.chr19:59027764G>A c.1277C>T c.(1276-1278)tCg>tTg p.S426L COAD 19 59027797 59027797 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr19:59027797C>T c.1244G>A c.(1243-1245)cGg>cAg p.R415Q COAD 19 59027840 59027840 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr19:59027840G>A c.1201C>T c.(1201-1203)Cct>Tct p.P401S COAD 19 59028171 59028171 + Silent SNP A A G TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr19:59028171A>G c.870T>C c.(868-870)acT>acC p.T290T COADREAD 19 59027797 59027797 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr19:59027797C>T c.1244G>A c.(1243-1245)cGg>cAg p.R415Q COADREAD 19 59027840 59027840 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr19:59027840G>A c.1201C>T c.(1201-1203)Cct>Tct p.P401S COADREAD 19 59028171 59028171 + Silent SNP A A G TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr19:59028171A>G c.870T>C c.(868-870)acT>acC p.T290T GBMLGG 19 59028371 59028371 + Missense_Mutation SNP C C T TCGA-DB-A64L-01A-11D-A29Q-08 TCGA-DB-A64L-10A-01D-A29Q-08 g.chr19:59028371C>T c.670G>A c.(670-672)Gaa>Aaa p.E224K GBMLGG 19 59028463 59028463 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:59028463G>T c.578C>A c.(577-579)cCt>cAt p.P193H GBMLGG 19 59028510 59028510 + Silent SNP C C T TCGA-DU-A6S2-01A-21D-A32B-08 TCGA-DU-A6S2-10A-01D-A329-08 g.chr19:59028510C>T c.531G>A c.(529-531)gcG>gcA p.A177A GBMLGG 19 59028593 59028593 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:59028593G>A c.448C>T c.(448-450)Cgt>Tgt p.R150C GBMLGG 19 59028726 59028726 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:59028726G>A c.315C>T c.(313-315)gcC>gcT p.A105A GBMLGG 19 59028924 59028924 + Missense_Mutation SNP A A C TCGA-FG-7641-01B-11D-2253-08 TCGA-FG-7641-10A-01D-2253-08 g.chr19:59028924A>C c.117T>G c.(115-117)atT>atG p.I39M HNSC 19 59028060 59028060 + Silent SNP C C T TCGA-CV-7104-01A-11D-2012-08 TCGA-CV-7104-10A-01D-2013-08 g.chr19:59028060C>T c.981G>A c.(979-981)ccG>ccA p.P327P HNSC 19 59028362 59028362 + Missense_Mutation SNP C C T TCGA-CQ-7064-01A-11D-2394-08 TCGA-CQ-7064-10A-01D-2394-08 g.chr19:59028362C>T c.679G>A c.(679-681)Ggc>Agc p.G227S HNSC 19 59028386 59028386 + Missense_Mutation SNP C C T TCGA-CN-4740-01A-01D-1434-08 TCGA-CN-4740-10A-01D-1434-08 g.chr19:59028386C>T c.655G>A c.(655-657)Gat>Aat p.D219N HNSC 19 59028615 59028615 + Silent SNP C C T TCGA-BA-6872-01A-11D-1870-08 TCGA-BA-6872-10A-01D-1870-08 g.chr19:59028615C>T c.426G>A c.(424-426)ccG>ccA p.P142P HNSC 19 59028764 59028764 + Missense_Mutation SNP C C T TCGA-CV-A6JY-01A-11D-A31L-08 TCGA-CV-A6JY-10A-01D-A31J-08 g.chr19:59028764C>T c.277G>A c.(277-279)Gtt>Att p.V93I HNSC 19 59028821 59028821 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr19:59028821C>T c.220G>A c.(220-222)Gtg>Atg p.V74M HNSC 19 59028822 59028822 + Silent SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr19:59028822C>T c.219G>A c.(217-219)ccG>ccA p.P73P HNSC 19 59028991 59028991 + Missense_Mutation SNP C C T TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr19:59028991C>T c.50G>A c.(49-51)cGc>cAc p.R17H LGG 19 59028371 59028371 + Missense_Mutation SNP C C T TCGA-DB-A64L-01A-11D-A29Q-08 TCGA-DB-A64L-10A-01D-A29Q-08 g.chr19:59028371C>T c.670G>A c.(670-672)Gaa>Aaa p.E224K LGG 19 59028463 59028463 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:59028463G>T c.578C>A c.(577-579)cCt>cAt p.P193H LGG 19 59028510 59028510 + Silent SNP C C T TCGA-DU-A6S2-01A-21D-A32B-08 TCGA-DU-A6S2-10A-01D-A329-08 g.chr19:59028510C>T c.531G>A c.(529-531)gcG>gcA p.A177A LGG 19 59028593 59028593 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:59028593G>A c.448C>T c.(448-450)Cgt>Tgt p.R150C LGG 19 59028726 59028726 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:59028726G>A c.315C>T c.(313-315)gcC>gcT p.A105A LGG 19 59028924 59028924 + Missense_Mutation SNP A A C TCGA-FG-7641-01B-11D-2253-08 TCGA-FG-7641-10A-01D-2253-08 g.chr19:59028924A>C c.117T>G c.(115-117)atT>atG p.I39M LIHC 19 59027809 59027809 + Missense_Mutation SNP G G A TCGA-ED-A97K-01A-21D-A382-10 TCGA-ED-A97K-10A-01D-A385-10 g.chr19:59027809G>A c.1232C>T c.(1231-1233)aCg>aTg p.T411M LIHC 19 59029036 59029036 + Missense_Mutation SNP G G A TCGA-HP-A5MZ-01A-21D-A27I-10 TCGA-HP-A5MZ-10A-01D-A27I-10 g.chr19:59029036G>A c.5C>T c.(4-6)gCg>gTg p.A2V LUAD 19 59027778 59027778 + Missense_Mutation SNP G G T TCGA-38-4632-01A-01D-1753-08 TCGA-38-4632-11A-01D-1753-08 g.chr19:59027778G>T c.1263C>A c.(1261-1263)caC>caA p.H421Q LUAD 19 59028204 59028204 + Silent SNP A A C TCGA-80-5608-01A-31D-1945-08 TCGA-80-5608-10A-01D-1946-08 g.chr19:59028204A>C c.837T>G c.(835-837)gcT>gcG p.A279A LUAD 19 59028392 59028392 + Missense_Mutation SNP C C T TCGA-05-5715-01A-01D-1625-08 TCGA-05-5715-10A-01D-1625-08 g.chr19:59028392C>T c.649G>A c.(649-651)Gag>Aag p.E217K LUAD 19 59028440 59028440 + Missense_Mutation SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr19:59028440C>T c.601G>A c.(601-603)Gcg>Acg p.A201T LUAD 19 59028515 59028515 + Missense_Mutation SNP G G T TCGA-55-6972-01A-11D-1945-08 TCGA-55-6972-11A-01D-1945-08 g.chr19:59028515G>T c.526C>A c.(526-528)Ccc>Acc p.P176T LUAD 19 59028554 59028554 + Missense_Mutation SNP C C A TCGA-75-5146-01A-01D-1625-08 TCGA-75-5146-10A-01D-1625-08 g.chr19:59028554C>A c.487G>T c.(487-489)Ggg>Tgg p.G163W LUAD 19 59028649 59028649 + Missense_Mutation SNP G G A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr19:59028649G>A c.392C>T c.(391-393)tCt>tTt p.S131F LUSC 19 59028370 59028370 + Missense_Mutation SNP T T A TCGA-60-2722-01A-01D-1522-08 TCGA-60-2722-11A-01D-1522-08 g.chr19:59028370T>A c.671A>T c.(670-672)gAa>gTa p.E224V PAAD 19 59027844 59027844 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:59027844C>T c.1197G>A c.(1195-1197)gaG>gaA p.E399E PAAD 19 59027866 59027866 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:59027866G>A c.1175C>T c.(1174-1176)cCt>cTt p.P392L PAAD 19 59028114 59028114 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:59028114C>A c.927G>T c.(925-927)caG>caT p.Q309H PAAD 19 59028774 59028774 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:59028774G>A c.267C>T c.(265-267)agC>agT p.S89S PCPG 19 59028621 59028621 + Silent SNP C C G TCGA-QR-A70O-01A-11D-A35D-08 TCGA-QR-A70O-10A-01D-A35B-08 g.chr19:59028621C>G c.420G>C c.(418-420)gtG>gtC p.V140V SARC 19 59025634 59025634 + Silent SNP A A C TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr19:59025634A>C c.1323T>G c.(1321-1323)tcT>tcG p.S441S SKCM 19 59025623 59025623 + Missense_Mutation SNP T T C TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr19:59025623T>C c.1334A>G c.(1333-1335)tAc>tGc p.Y445C SKCM 19 59028057 59028057 + Silent SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr19:59028057G>A c.984C>T c.(982-984)ccC>ccT p.P328P SKCM 19 59028285 59028285 + Silent SNP C C T TCGA-ER-A197-06A-32D-A197-08 TCGA-ER-A197-10A-01D-A199-08 g.chr19:59028285C>T c.756G>A c.(754-756)gcG>gcA p.A252A SKCM 19 59028308 59028308 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr19:59028308G>A c.733C>T c.(733-735)Ctc>Ttc p.L245F SKCM 19 59028416 59028416 + Missense_Mutation SNP C C G TCGA-D3-A1QA-06A-11D-A196-08 TCGA-D3-A1QA-10A-01D-A198-08 g.chr19:59028416C>G c.625G>C c.(625-627)Gag>Cag p.E209Q SKCM 19 59028743 59028743 + Silent SNP G G A TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr19:59028743G>A c.298C>T c.(298-300)Ctg>Ttg p.L100L SKCM 19 59028923 59028923 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr19:59028923G>A c.118C>T c.(118-120)Cgt>Tgt p.R40C

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 19 59028457 59028457 single base substitution G A downstream_gene_variant BLCA-CN 19 59028457 59028457 single base substitution G A missense_variant A195V 584C>T BLCA-CN 19 59029027 59029027 single base substitution T G missense_variant E5A 14A>C BLCA-US 19 59022230 59022230 single base substitution G A downstream_gene_variant BLCA-US 19 59025544 59025544 single base substitution C T downstream_gene_variant BLCA-US 19 59025544 59025544 single base substitution C T synonymous_variant K471K 1413G>A BLCA-US 19 59028353 59028353 single base substitution C T downstream_gene_variant BLCA-US 19 59028353 59028353 single base substitution C T missense_variant E230K 688G>A BLCA-US 19 59028486 59028486 single base substitution T C downstream_gene_variant BLCA-US 19 59028486 59028486 single base substitution T C synonymous_variant P185P 555A>G BLCA-US 19 59028629 59028629 single base substitution T G downstream_gene_variant BLCA-US 19 59028629 59028629 single base substitution T G missense_variant T138P 412A>C BOCA-FR 19 59023859 59023859 single base substitution T A downstream_gene_variant BOCA-FR 19 59034341 59034341 single base substitution G A intron_variant BOCA-FR 19 59034341 59034341 single base substitution G A upstream_gene_variant BOCA-FR 19 59050659 59050659 single base substitution C T upstream_gene_variant BRCA-EU 19 59020062 59020062 single base substitution C G downstream_gene_variant BRCA-EU 19 59022580 59022580 single base substitution C A downstream_gene_variant BRCA-EU 19 59022761 59022761 single base substitution G T downstream_gene_variant BRCA-EU 19 59024415 59024415 single base substitution G A downstream_gene_variant BRCA-EU 19 59025507 59025507 single base substitution C G downstream_gene_variant BRCA-EU 19 59025507 59025507 single base substitution C G missense_variant E484Q 1450G>C BRCA-EU 19 59028671 59028671 single base substitution G A downstream_gene_variant BRCA-EU 19 59028671 59028671 single base substitution G A missense_variant R124C 370C>T BRCA-EU 19 59029031 59029031 single base substitution C T missense_variant A4T 10G>A BRCA-EU 19 59029334 59029334 single base substitution G A intron_variant BRCA-EU 19 59030200 59030200 single base substitution C T intron_variant BRCA-EU 19 59030803 59030803 single base substitution C T 5_prime_UTR_variant BRCA-EU 19 59030803 59030803 single base substitution C T intron_variant BRCA-EU 19 59033673 59033673 single base substitution C T intron_variant BRCA-EU 19 59033673 59033673 single base substitution C T upstream_gene_variant BRCA-EU 19 59034848 59034848 single base substitution G C intron_variant BRCA-EU 19 59034848 59034848 single base substitution G C upstream_gene_variant BRCA-EU 19 59034931 59034931 single base substitution T A intron_variant BRCA-EU 19 59034931 59034931 single base substitution T A upstream_gene_variant BRCA-EU 19 59036500 59036500 single base substitution C G intron_variant BRCA-EU 19 59036500 59036500 single base substitution C G upstream_gene_variant BRCA-EU 19 59037426 59037426 single base substitution C T intron_variant BRCA-EU 19 59037818 59037818 single base substitution C G intron_variant BRCA-EU 19 59038537 59038537 single base substitution A G intron_variant BRCA-EU 19 59038553 59038553 single base substitution C T intron_variant BRCA-EU 19 59039122 59039122 single base substitution C G intron_variant BRCA-EU 19 59040216 59040216 single base substitution G A intron_variant BRCA-EU 19 59040222 59040222 single base substitution C T intron_variant BRCA-EU 19 59041546 59041546 single base substitution G A intron_variant BRCA-EU 19 59041685 59041685 deletion of <=200bp T - intron_variant BRCA-EU 19 59041793 59041793 single base substitution C T intron_variant BRCA-EU 19 59041926 59041926 single base substitution G T intron_variant BRCA-EU 19 59042120 59042120 single base substitution G T intron_variant BRCA-EU 19 59042279 59042279 single base substitution C T intron_variant BRCA-EU 19 59043079 59043079 single base substitution A T intron_variant BRCA-EU 19 59043708 59043708 single base substitution G A intron_variant BRCA-EU 19 59044720 59044720 single base substitution C T intron_variant BRCA-EU 19 59045369 59045369 deletion of <=200bp G - intron_variant BRCA-EU 19 59045410 59045410 single base substitution C T intron_variant BRCA-EU 19 59045751 59045753 deletion of <=200bp TAT - intron_variant BRCA-EU 19 59050190 59050190 single base substitution G A 5_prime_UTR_variant BRCA-EU 19 59050842 59050842 single base substitution G A upstream_gene_variant BRCA-EU 19 59051105 59051105 single base substitution C T upstream_gene_variant BRCA-EU 19 59051503 59051503 single base substitution T G upstream_gene_variant BRCA-EU 19 59052018 59052018 single base substitution C G upstream_gene_variant BRCA-EU 19 59053156 59053156 single base substitution C G upstream_gene_variant BRCA-EU 19 59053585 59053585 single base substitution A G upstream_gene_variant BRCA-EU 19 59053761 59053761 single base substitution C G upstream_gene_variant BRCA-EU 19 59054338 59054338 single base substitution C T upstream_gene_variant BRCA-EU 19 59054480 59054480 single base substitution G T upstream_gene_variant BRCA-FR 19 59021508 59021508 single base substitution T A downstream_gene_variant BRCA-FR 19 59034848 59034848 single base substitution G C intron_variant BRCA-FR 19 59034848 59034848 single base substitution G C upstream_gene_variant BRCA-FR 19 59041546 59041546 single base substitution G A intron_variant BRCA-FR 19 59042120 59042120 single base substitution G T intron_variant BRCA-FR 19 59048541 59048541 single base substitution A G intron_variant BRCA-FR 19 59049691 59049691 single base substitution C T intron_variant BRCA-UK 19 59021849 59021849 single base substitution G C downstream_gene_variant BRCA-UK 19 59028841 59028841 single base substitution G A downstream_gene_variant BRCA-UK 19 59028841 59028841 single base substitution G A missense_variant S67F 200C>T BRCA-UK 19 59028881 59028881 single base substitution C T downstream_gene_variant BRCA-UK 19 59028881 59028881 single base substitution C T missense_variant G54S 160G>A BRCA-UK 19 59053178 59053178 single base substitution C G upstream_gene_variant BRCA-US 19 59021339 59021339 single base substitution C T downstream_gene_variant BRCA-US 19 59022779 59022779 insertion of <=200bp - C downstream_gene_variant BRCA-US 19 59028713 59028713 single base substitution G A downstream_gene_variant BRCA-US 19 59028713 59028713 single base substitution G A missense_variant R110C 328C>T BTCA-JP 19 59022144 59022144 single base substitution C T downstream_gene_variant CESC-US 19 59021320 59021320 single base substitution C G downstream_gene_variant CESC-US 19 59021339 59021339 single base substitution C T downstream_gene_variant CESC-US 19 59022833 59022833 single base substitution C G downstream_gene_variant CESC-US 19 59022902 59022902 single base substitution C T downstream_gene_variant CESC-US 19 59025616 59025616 single base substitution G C downstream_gene_variant CESC-US 19 59025616 59025616 single base substitution G C synonymous_variant L447L 1341C>G CESC-US 19 59027764 59027764 single base substitution G A downstream_gene_variant CESC-US 19 59027764 59027764 single base substitution G A missense_variant S426L 1277C>T CLLE-ES 19 59051294 59051294 single base substitution T C upstream_gene_variant CLLE-ES 19 59054112 59054112 single base substitution G C upstream_gene_variant COAD-US 19 59021349 59021349 single base substitution T C downstream_gene_variant COAD-US 19 59023166 59023166 single base substitution G A downstream_gene_variant COAD-US 19 59023174 59023174 single base substitution A G downstream_gene_variant COAD-US 19 59023239 59023239 single base substitution A G downstream_gene_variant COAD-US 19 59023241 59023241 single base substitution C T downstream_gene_variant COAD-US 19 59023253 59023253 single base substitution C T downstream_gene_variant COAD-US 19 59027797 59027797 single base substitution C T downstream_gene_variant COAD-US 19 59027797 59027797 single base substitution C T missense_variant R415Q 1244G>A COAD-US 19 59027840 59027840 single base substitution G A downstream_gene_variant COAD-US 19 59027840 59027840 single base substitution G A missense_variant P401S 1201C>T COAD-US 19 59028171 59028171 single base substitution A G downstream_gene_variant COAD-US 19 59028171 59028171 single base substitution A G synonymous_variant T290T 870T>C COAD-US 19 59028672 59028672 single base substitution G A downstream_gene_variant COAD-US 19 59028672 59028672 single base substitution G A synonymous_variant A123A 369C>T COCA-CN 19 59025375 59025375 single base substitution C T 3_prime_UTR_variant COCA-CN 19 59025375 59025375 single base substitution C T downstream_gene_variant COCA-CN 19 59028813 59028813 single base substitution G A downstream_gene_variant COCA-CN 19 59028813 59028813 single base substitution G A synonymous_variant P76P 228C>T COCA-CN 19 59050387 59050387 single base substitution T A upstream_gene_variant EOPC-DE 19 59039198 59039198 single base substitution A C intron_variant EOPC-DE 19 59040222 59040222 single base substitution C T intron_variant ESAD-UK 19 59020623 59020623 single base substitution G A downstream_gene_variant ESAD-UK 19 59021592 59021592 single base substitution A G downstream_gene_variant ESAD-UK 19 59022173 59022173 single base substitution C T downstream_gene_variant ESAD-UK 19 59023944 59023944 single base substitution C T downstream_gene_variant ESAD-UK 19 59025223 59025223 single base substitution C T 3_prime_UTR_variant ESAD-UK 19 59025223 59025223 single base substitution C T downstream_gene_variant ESAD-UK 19 59027992 59027992 single base substitution G A downstream_gene_variant ESAD-UK 19 59027992 59027992 single base substitution G A missense_variant S350L 1049C>T ESAD-UK 19 59028992 59028992 single base substitution G A missense_variant R17C 49C>T ESAD-UK 19 59030002 59030002 single base substitution G A intron_variant ESAD-UK 19 59030094 59030094 single base substitution G A intron_variant ESAD-UK 19 59031287 59031287 single base substitution C A 5_prime_UTR_variant ESAD-UK 19 59031287 59031287 single base substitution C A intron_variant ESAD-UK 19 59031287 59031287 single base substitution C A upstream_gene_variant ESAD-UK 19 59033280 59033280 single base substitution G A intron_variant ESAD-UK 19 59033280 59033280 single base substitution G A upstream_gene_variant ESAD-UK 19 59034008 59034008 insertion of <=200bp - A intron_variant ESAD-UK 19 59034008 59034008 insertion of <=200bp - A upstream_gene_variant ESAD-UK 19 59034867 59034867 single base substitution G A intron_variant ESAD-UK 19 59034867 59034867 single base substitution G A upstream_gene_variant ESAD-UK 19 59038356 59038356 single base substitution G A intron_variant ESAD-UK 19 59038651 59038651 single base substitution A G intron_variant ESAD-UK 19 59040753 59040753 single base substitution G A intron_variant ESAD-UK 19 59042280 59042280 single base substitution G A intron_variant ESAD-UK 19 59042684 59042684 single base substitution T C intron_variant ESAD-UK 19 59044387 59044387 single base substitution G C intron_variant ESAD-UK 19 59044694 59044694 single base substitution A G intron_variant ESAD-UK 19 59047079 59047079 single base substitution A T intron_variant ESAD-UK 19 59047365 59047365 single base substitution C A intron_variant ESAD-UK 19 59047570 59047570 single base substitution C T intron_variant ESAD-UK 19 59048251 59048251 single base substitution C T intron_variant ESAD-UK 19 59051099 59051101 deletion of <=200bp CCT - upstream_gene_variant ESAD-UK 19 59054312 59054312 single base substitution T G upstream_gene_variant ESAD-UK 19 59054688 59054688 single base substitution C T upstream_gene_variant ESAD-UK 19 59054853 59054853 single base substitution C A upstream_gene_variant ESCA-CN 19 59022808 59022808 single base substitution C G downstream_gene_variant KIRP-US 19 59027831 59027831 single base substitution C G downstream_gene_variant KIRP-US 19 59027831 59027831 single base substitution C G missense_variant E404Q 1210G>C LAML-KR 19 59037901 59037901 single base substitution T A intron_variant LAML-KR 19 59044180 59044180 single base substitution T C intron_variant LAML-KR 19 59047892 59047892 single base substitution T C intron_variant LAML-KR 19 59050624 59050624 single base substitution C A upstream_gene_variant LAML-KR 19 59050665 59050665 single base substitution G C upstream_gene_variant LAML-KR 19 59051013 59051013 single base substitution C G upstream_gene_variant LAML-KR 19 59051612 59051612 single base substitution T G upstream_gene_variant LAML-KR 19 59051666 59051666 single base substitution A C upstream_gene_variant LAML-KR 19 59051974 59051974 single base substitution C A upstream_gene_variant LAML-KR 19 59052210 59052210 single base substitution G C upstream_gene_variant LAML-KR 19 59052645 59052645 single base substitution G A upstream_gene_variant LAML-KR 19 59052703 59052703 single base substitution T G upstream_gene_variant LAML-KR 19 59052986 59052986 single base substitution C G upstream_gene_variant LAML-KR 19 59053243 59053243 single base substitution C T upstream_gene_variant LAML-KR 19 59053448 59053448 single base substitution G C upstream_gene_variant LAML-KR 19 59053720 59053720 single base substitution T C upstream_gene_variant LAML-KR 19 59053761 59053761 single base substitution C G upstream_gene_variant LGG-US 19 59028371 59028371 single base substitution C T downstream_gene_variant LGG-US 19 59028371 59028371 single base substitution C T missense_variant E224K 670G>A LGG-US 19 59028924 59028924 single base substitution A C downstream_gene_variant LGG-US 19 59028924 59028924 single base substitution A C missense_variant I39M 117T>G LICA-FR 19 59023108 59023156 deletion of <=200bp GCCAGGGCCGCAGCTGCCAGGCTCAGCCCATGGGGCACCCAGGGGCCGA - downstream_gene_variant LICA-FR 19 59024303 59024303 single base substitution T G downstream_gene_variant LICA-FR 19 59031512 59031512 single base substitution C T 5_prime_UTR_variant LICA-FR 19 59031512 59031512 single base substitution C T intron_variant LICA-FR 19 59031512 59031512 single base substitution C T upstream_gene_variant LICA-FR 19 59034285 59034285 single base substitution G T intron_variant LICA-FR 19 59034285 59034285 single base substitution G T upstream_gene_variant LICA-FR 19 59037897 59037897 single base substitution T A intron_variant LICA-FR 19 59037900 59037900 single base substitution T A intron_variant LICA-FR 19 59047833 59047833 deletion of <=200bp A - intron_variant LICA-FR 19 59048500 59048500 single base substitution C A intron_variant LICA-FR 19 59050416 59050416 single base substitution G A upstream_gene_variant LICA-FR 19 59050472 59050472 single base substitution C A upstream_gene_variant LICA-FR 19 59050500 59050500 single base substitution T C upstream_gene_variant LICA-FR 19 59050628 59050628 single base substitution C T upstream_gene_variant LICA-FR 19 59050727 59050727 single base substitution T G upstream_gene_variant LICA-FR 19 59050965 59050965 single base substitution T C upstream_gene_variant LICA-FR 19 59051518 59051518 single base substitution C T upstream_gene_variant LICA-FR 19 59052361 59052361 single base substitution A C upstream_gene_variant LICA-FR 19 59052456 59052456 single base substitution T C upstream_gene_variant LICA-FR 19 59052509 59052509 single base substitution T A upstream_gene_variant LICA-FR 19 59052595 59052595 single base substitution A C upstream_gene_variant LICA-FR 19 59055161 59055161 single base substitution G C upstream_gene_variant LIHC-US 19 59022230 59022230 single base substitution G A downstream_gene_variant LIHC-US 19 59029036 59029036 single base substitution G A missense_variant A2V 5C>T LINC-JP 19 59021417 59021417 single base substitution A G downstream_gene_variant LINC-JP 19 59022818 59022818 single base substitution G C downstream_gene_variant LINC-JP 19 59022888 59022888 single base substitution A G downstream_gene_variant LINC-JP 19 59023004 59023004 single base substitution A C downstream_gene_variant LINC-JP 19 59023203 59023203 single base substitution G T downstream_gene_variant LINC-JP 19 59028253 59028253 single base substitution G A downstream_gene_variant LINC-JP 19 59028253 59028253 single base substitution G A missense_variant A263V 788C>T LINC-JP 19 59028395 59028395 single base substitution C A downstream_gene_variant LINC-JP 19 59028395 59028395 single base substitution C A missense_variant D216Y 646G>T LINC-JP 19 59028693 59028693 single base substitution G A downstream_gene_variant LINC-JP 19 59028693 59028693 single base substitution G A synonymous_variant D116D 348C>T LINC-JP 19 59036985 59036985 single base substitution A C intron_variant LIRI-JP 19 59030180 59030180 single base substitution T C intron_variant LIRI-JP 19 59037279 59037279 single base substitution T C intron_variant LIRI-JP 19 59043094 59043094 single base substitution A G intron_variant LIRI-JP 19 59048388 59048388 single base substitution G C intron_variant LUSC-KR 19 59021540 59021540 single base substitution G C downstream_gene_variant LUSC-KR 19 59024869 59024869 single base substitution G T downstream_gene_variant LUSC-KR 19 59026342 59026342 single base substitution G T downstream_gene_variant LUSC-KR 19 59026342 59026342 single base substitution G T intron_variant LUSC-KR 19 59031669 59031669 single base substitution C T intron_variant LUSC-KR 19 59031669 59031669 single base substitution C T upstream_gene_variant LUSC-KR 19 59033770 59033770 single base substitution C T intron_variant LUSC-KR 19 59033770 59033770 single base substitution C T upstream_gene_variant LUSC-KR 19 59037575 59037575 single base substitution T C intron_variant LUSC-KR 19 59037897 59037897 single base substitution T A intron_variant LUSC-KR 19 59037900 59037900 single base substitution T A intron_variant LUSC-KR 19 59037901 59037901 single base substitution T A intron_variant LUSC-KR 19 59037902 59037902 single base substitution T A intron_variant LUSC-KR 19 59039808 59039808 single base substitution C T intron_variant LUSC-KR 19 59040445 59040445 single base substitution C A intron_variant LUSC-KR 19 59045907 59045907 single base substitution C A intron_variant LUSC-KR 19 59045908 59045908 single base substitution C A intron_variant LUSC-KR 19 59049490 59049490 single base substitution C A intron_variant LUSC-KR 19 59050209 59050209 single base substitution C A 5_prime_UTR_variant LUSC-KR 19 59050550 59050550 single base substitution C A upstream_gene_variant LUSC-KR 19 59050621 59050621 single base substitution A C upstream_gene_variant LUSC-KR 19 59050628 59050628 single base substitution C T upstream_gene_variant LUSC-KR 19 59050774 59050774 single base substitution A C upstream_gene_variant LUSC-KR 19 59050779 59050779 single base substitution C G upstream_gene_variant LUSC-KR 19 59051166 59051166 single base substitution G C upstream_gene_variant LUSC-KR 19 59051432 59051432 single base substitution C A upstream_gene_variant LUSC-KR 19 59051584 59051584 single base substitution T C upstream_gene_variant LUSC-KR 19 59051632 59051632 single base substitution C G upstream_gene_variant LUSC-KR 19 59051666 59051666 single base substitution A C upstream_gene_variant LUSC-KR 19 59051671 59051671 single base substitution G C upstream_gene_variant LUSC-KR 19 59051975 59051975 single base substitution C G upstream_gene_variant LUSC-KR 19 59052191 59052191 single base substitution G A upstream_gene_variant LUSC-KR 19 59052496 59052496 single base substitution T A upstream_gene_variant LUSC-KR 19 59052760 59052760 single base substitution G A upstream_gene_variant LUSC-KR 19 59052979 59052979 single base substitution T C upstream_gene_variant LUSC-KR 19 59053057 59053057 single base substitution C T upstream_gene_variant LUSC-KR 19 59053487 59053487 single base substitution G C upstream_gene_variant LUSC-KR 19 59053800 59053800 single base substitution G C upstream_gene_variant LUSC-KR 19 59053878 59053878 single base substitution C A upstream_gene_variant LUSC-KR 19 59053942 59053942 single base substitution C T upstream_gene_variant LUSC-KR 19 59053950 59053950 single base substitution T A upstream_gene_variant LUSC-KR 19 59053973 59053973 single base substitution G A upstream_gene_variant LUSC-KR 19 59054112 59054112 single base substitution G C upstream_gene_variant LUSC-US 19 59021301 59021301 single base substitution C A downstream_gene_variant LUSC-US 19 59028370 59028370 single base substitution T A downstream_gene_variant LUSC-US 19 59028370 59028370 single base substitution T A missense_variant E224V 671A>T MALY-DE 19 59028288 59028288 single base substitution G A downstream_gene_variant MALY-DE 19 59028288 59028288 single base substitution G A synonymous_variant S251S 753C>T MALY-DE 19 59041250 59041250 single base substitution T C intron_variant MALY-DE 19 59041928 59041928 single base substitution C T intron_variant MALY-DE 19 59042465 59042465 single base substitution T C intron_variant MALY-DE 19 59047189 59047189 single base substitution C T intron_variant MALY-DE 19 59054299 59054304 deletion of <=200bp GTTGAG - upstream_gene_variant MALY-DE 19 59054514 59054514 single base substitution C T upstream_gene_variant MELA-AU 19 59020152 59020152 single base substitution A T downstream_gene_variant MELA-AU 19 59020275 59020275 single base substitution C T downstream_gene_variant MELA-AU 19 59020903 59020903 single base substitution C T downstream_gene_variant MELA-AU 19 59021243 59021243 single base substitution A T downstream_gene_variant MELA-AU 19 59021741 59021741 single base substitution G A downstream_gene_variant MELA-AU 19 59021851 59021851 single base substitution G A downstream_gene_variant MELA-AU 19 59022135 59022135 single base substitution A G downstream_gene_variant MELA-AU 19 59022287 59022287 single base substitution C T downstream_gene_variant MELA-AU 19 59022406 59022406 single base substitution C G downstream_gene_variant MELA-AU 19 59022473 59022473 single base substitution C T downstream_gene_variant MELA-AU 19 59022777 59022777 single base substitution G A downstream_gene_variant MELA-AU 19 59023784 59023784 single base substitution C T downstream_gene_variant MELA-AU 19 59024279 59024279 single base substitution G A downstream_gene_variant MELA-AU 19 59026007 59026007 single base substitution G A downstream_gene_variant MELA-AU 19 59026007 59026007 single base substitution G A intron_variant MELA-AU 19 59027346 59027346 single base substitution C T downstream_gene_variant MELA-AU 19 59027346 59027346 single base substitution C T intron_variant MELA-AU 19 59027967 59027967 single base substitution G A downstream_gene_variant MELA-AU 19 59027967 59027967 single base substitution G A synonymous_variant P358P 1074C>T MELA-AU 19 59028874 59028874 single base substitution G A downstream_gene_variant MELA-AU 19 59028874 59028874 single base substitution G A missense_variant P56L 167C>T MELA-AU 19 59030813 59030813 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 19 59030813 59030813 single base substitution G A intron_variant MELA-AU 19 59031133 59031133 single base substitution G A 5_prime_UTR_variant MELA-AU 19 59031133 59031133 single base substitution G A intron_variant MELA-AU 19 59031133 59031133 single base substitution G A upstream_gene_variant MELA-AU 19 59031373 59031373 single base substitution C T 5_prime_UTR_variant MELA-AU 19 59031373 59031373 single base substitution C T intron_variant MELA-AU 19 59031373 59031373 single base substitution C T upstream_gene_variant MELA-AU 19 59033301 59033301 single base substitution C T intron_variant MELA-AU 19 59033301 59033301 single base substitution C T upstream_gene_variant MELA-AU 19 59033430 59033430 single base substitution C T intron_variant MELA-AU 19 59033430 59033430 single base substitution C T upstream_gene_variant MELA-AU 19 59033906 59033906 single base substitution G C intron_variant MELA-AU 19 59033906 59033906 single base substitution G C upstream_gene_variant MELA-AU 19 59034108 59034109 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 59034108 59034109 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 59034587 59034587 single base substitution C T intron_variant MELA-AU 19 59034587 59034587 single base substitution C T upstream_gene_variant MELA-AU 19 59034704 59034704 single base substitution G T intron_variant MELA-AU 19 59034704 59034704 single base substitution G T upstream_gene_variant MELA-AU 19 59035028 59035028 single base substitution C T intron_variant MELA-AU 19 59035028 59035028 single base substitution C T upstream_gene_variant MELA-AU 19 59036477 59036477 single base substitution C T intron_variant MELA-AU 19 59036477 59036477 single base substitution C T upstream_gene_variant MELA-AU 19 59036643 59036643 single base substitution G A intron_variant MELA-AU 19 59036644 59036644 single base substitution G A intron_variant MELA-AU 19 59036941 59036941 single base substitution G A intron_variant MELA-AU 19 59036996 59036996 single base substitution G A intron_variant MELA-AU 19 59037018 59037018 single base substitution G A intron_variant MELA-AU 19 59037086 59037086 single base substitution G A intron_variant MELA-AU 19 59037087 59037087 single base substitution G A intron_variant MELA-AU 19 59037458 59037458 single base substitution G A intron_variant MELA-AU 19 59037477 59037477 single base substitution C T intron_variant MELA-AU 19 59037513 59037513 single base substitution C T intron_variant MELA-AU 19 59037621 59037621 single base substitution G A intron_variant MELA-AU 19 59037826 59037826 single base substitution C T intron_variant MELA-AU 19 59038387 59038387 single base substitution A G intron_variant MELA-AU 19 59038388 59038388 single base substitution G A intron_variant MELA-AU 19 59038404 59038404 single base substitution C T intron_variant MELA-AU 19 59038409 59038409 single base substitution C T intron_variant MELA-AU 19 59038421 59038421 single base substitution G A intron_variant MELA-AU 19 59038766 59038766 single base substitution G T intron_variant MELA-AU 19 59038993 59038993 single base substitution G A intron_variant MELA-AU 19 59039258 59039258 single base substitution C T intron_variant MELA-AU 19 59039809 59039809 single base substitution G A intron_variant MELA-AU 19 59039906 59039906 single base substitution C T intron_variant MELA-AU 19 59040433 59040433 single base substitution G A intron_variant MELA-AU 19 59040586 59040586 single base substitution C T intron_variant MELA-AU 19 59040722 59040722 single base substitution G A intron_variant MELA-AU 19 59040816 59040816 single base substitution A G intron_variant MELA-AU 19 59040920 59040920 single base substitution C T intron_variant MELA-AU 19 59040932 59040932 single base substitution G A intron_variant MELA-AU 19 59040978 59040978 single base substitution G A intron_variant MELA-AU 19 59041162 59041162 single base substitution G A intron_variant MELA-AU 19 59041219 59041219 single base substitution C G intron_variant MELA-AU 19 59041741 59041741 single base substitution C A intron_variant MELA-AU 19 59041797 59041797 single base substitution C T intron_variant MELA-AU 19 59041809 59041809 single base substitution G A intron_variant MELA-AU 19 59041871 59041871 single base substitution C T intron_variant MELA-AU 19 59041906 59041906 single base substitution C A intron_variant MELA-AU 19 59042158 59042158 single base substitution C T intron_variant MELA-AU 19 59042185 59042185 single base substitution G A intron_variant MELA-AU 19 59042307 59042307 single base substitution C T intron_variant MELA-AU 19 59042387 59042387 single base substitution G A intron_variant MELA-AU 19 59042405 59042405 single base substitution C T intron_variant MELA-AU 19 59042649 59042649 single base substitution C G intron_variant MELA-AU 19 59042690 59042690 single base substitution C G intron_variant MELA-AU 19 59042739 59042739 single base substitution C T intron_variant MELA-AU 19 59042823 59042823 single base substitution C T intron_variant MELA-AU 19 59042835 59042835 single base substitution C G intron_variant MELA-AU 19 59042902 59042902 single base substitution C T intron_variant MELA-AU 19 59042919 59042919 single base substitution T G intron_variant MELA-AU 19 59042934 59042934 single base substitution C G intron_variant MELA-AU 19 59042985 59042985 single base substitution C T intron_variant MELA-AU 19 59043091 59043091 single base substitution G T intron_variant MELA-AU 19 59043093 59043093 single base substitution G A intron_variant MELA-AU 19 59043295 59043295 single base substitution C T intron_variant MELA-AU 19 59043334 59043334 single base substitution C T intron_variant MELA-AU 19 59043373 59043373 single base substitution C T intron_variant MELA-AU 19 59043453 59043453 single base substitution G A intron_variant MELA-AU 19 59043473 59043473 single base substitution C T intron_variant MELA-AU 19 59043565 59043565 single base substitution G A intron_variant MELA-AU 19 59043594 59043594 single base substitution G A intron_variant MELA-AU 19 59043998 59043998 single base substitution C T intron_variant MELA-AU 19 59044072 59044072 single base substitution C T intron_variant MELA-AU 19 59044402 59044402 single base substitution C T intron_variant MELA-AU 19 59044461 59044461 single base substitution C T intron_variant MELA-AU 19 59044498 59044498 single base substitution C T intron_variant MELA-AU 19 59044559 59044559 single base substitution G A intron_variant MELA-AU 19 59044731 59044731 single base substitution G A intron_variant MELA-AU 19 59045575 59045575 single base substitution C T intron_variant MELA-AU 19 59045595 59045595 single base substitution G A intron_variant MELA-AU 19 59045820 59045820 single base substitution G A intron_variant MELA-AU 19 59046109 59046109 single base substitution G T intron_variant MELA-AU 19 59046231 59046231 single base substitution T A intron_variant MELA-AU 19 59046823 59046823 single base substitution G A intron_variant MELA-AU 19 59046845 59046845 single base substitution T C intron_variant MELA-AU 19 59047005 59047005 single base substitution G A intron_variant MELA-AU 19 59047185 59047185 single base substitution C T intron_variant MELA-AU 19 59047420 59047420 single base substitution G A intron_variant MELA-AU 19 59047449 59047449 single base substitution G A intron_variant MELA-AU 19 59047668 59047668 single base substitution T G intron_variant MELA-AU 19 59047697 59047697 single base substitution G A intron_variant MELA-AU 19 59047700 59047700 single base substitution G T intron_variant MELA-AU 19 59047865 59047865 single base substitution C T intron_variant MELA-AU 19 59048174 59048174 single base substitution A G intron_variant MELA-AU 19 59048969 59048969 single base substitution G A intron_variant MELA-AU 19 59050242 59050242 single base substitution G A 5_prime_UTR_variant MELA-AU 19 59050376 59050376 single base substitution G A upstream_gene_variant MELA-AU 19 59050567 59050567 single base substitution G A upstream_gene_variant MELA-AU 19 59050846 59050846 single base substitution C T upstream_gene_variant MELA-AU 19 59051177 59051177 single base substitution C T upstream_gene_variant MELA-AU 19 59051254 59051254 single base substitution C T upstream_gene_variant MELA-AU 19 59051817 59051818 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 59051833 59051833 single base substitution C T upstream_gene_variant MELA-AU 19 59051872 59051872 single base substitution C T upstream_gene_variant MELA-AU 19 59052085 59052085 single base substitution T C upstream_gene_variant MELA-AU 19 59053279 59053280 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 59053771 59053771 single base substitution C T upstream_gene_variant MELA-AU 19 59053775 59053775 single base substitution C T upstream_gene_variant MELA-AU 19 59054228 59054229 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 59055235 59055235 single base substitution T G upstream_gene_variant ORCA-IN 19 59022682 59022682 single base substitution G A downstream_gene_variant ORCA-IN 19 59022806 59022806 single base substitution C G downstream_gene_variant ORCA-IN 19 59025565 59025565 single base substitution G T downstream_gene_variant ORCA-IN 19 59025565 59025565 single base substitution G T stop_gained C464* 1392C>A ORCA-IN 19 59035772 59035772 single base substitution A G intron_variant ORCA-IN 19 59035772 59035772 single base substitution A G upstream_gene_variant ORCA-IN 19 59043324 59043324 single base substitution C T intron_variant ORCA-IN 19 59045294 59045294 single base substitution C T intron_variant ORCA-IN 19 59052085 59052085 single base substitution T C upstream_gene_variant OV-AU 19 59026677 59026677 single base substitution G T downstream_gene_variant OV-AU 19 59026677 59026677 single base substitution G T intron_variant OV-AU 19 59035937 59035937 single base substitution T C intron_variant OV-AU 19 59035937 59035937 single base substitution T C upstream_gene_variant OV-AU 19 59042775 59042775 single base substitution C A intron_variant OV-AU 19 59042833 59042833 single base substitution C G intron_variant OV-AU 19 59050923 59050923 single base substitution G T upstream_gene_variant OV-AU 19 59051048 59051048 single base substitution C T upstream_gene_variant OV-AU 19 59052910 59052910 single base substitution C G upstream_gene_variant OV-AU 19 59054051 59054051 single base substitution A G upstream_gene_variant OV-AU 19 59054286 59054286 single base substitution G T upstream_gene_variant PACA-AU 19 59026692 59026692 single base substitution T A downstream_gene_variant PACA-AU 19 59026692 59026692 single base substitution T A intron_variant PACA-AU 19 59029100 59029100 single base substitution G T intron_variant PACA-AU 19 59037301 59037301 single base substitution A T intron_variant PACA-AU 19 59037903 59037903 single base substitution T A intron_variant PACA-AU 19 59038751 59038751 single base substitution C G intron_variant PACA-AU 19 59039893 59039893 single base substitution G A intron_variant PACA-AU 19 59042694 59042694 single base substitution A C intron_variant PACA-AU 19 59044499 59044499 single base substitution G A intron_variant PACA-AU 19 59046261 59046261 single base substitution G A intron_variant PACA-AU 19 59053211 59053211 single base substitution C T upstream_gene_variant PACA-CA 19 59022201 59022201 single base substitution C A downstream_gene_variant PACA-CA 19 59022667 59022667 single base substitution C G downstream_gene_variant PACA-CA 19 59023565 59023565 single base substitution G C downstream_gene_variant PACA-CA 19 59023840 59023840 single base substitution T C downstream_gene_variant PACA-CA 19 59025293 59025293 single base substitution G T 3_prime_UTR_variant PACA-CA 19 59025293 59025293 single base substitution G T downstream_gene_variant PACA-CA 19 59025316 59025316 single base substitution G C 3_prime_UTR_variant PACA-CA 19 59025316 59025316 single base substitution G C downstream_gene_variant PACA-CA 19 59025478 59025478 single base substitution C T downstream_gene_variant PACA-CA 19 59025478 59025478 single base substitution C T synonymous_variant K493K 1479G>A PACA-CA 19 59025480 59025480 single base substitution T G downstream_gene_variant PACA-CA 19 59025480 59025480 single base substitution T G missense_variant K493Q 1477A>C PACA-CA 19 59027710 59027710 single base substitution G A downstream_gene_variant PACA-CA 19 59027710 59027710 single base substitution G A intron_variant PACA-CA 19 59030794 59030794 single base substitution A G 5_prime_UTR_variant PACA-CA 19 59030794 59030794 single base substitution A G intron_variant PACA-CA 19 59031967 59031967 single base substitution G T intron_variant PACA-CA 19 59031967 59031967 single base substitution G T upstream_gene_variant PACA-CA 19 59040804 59040804 single base substitution G A intron_variant PACA-CA 19 59042200 59042200 single base substitution G A intron_variant PACA-CA 19 59045174 59045174 single base substitution C T intron_variant PACA-CA 19 59046602 59046602 single base substitution T G intron_variant PACA-CA 19 59046620 59046620 single base substitution G T intron_variant PACA-CA 19 59048009 59048009 insertion of <=200bp - A intron_variant PACA-CA 19 59049722 59049722 single base substitution T A intron_variant PACA-CA 19 59050581 59050581 single base substitution C T upstream_gene_variant PACA-CA 19 59050699 59050699 single base substitution A C upstream_gene_variant PACA-CA 19 59051006 59051006 single base substitution C T upstream_gene_variant PACA-CA 19 59051906 59051906 single base substitution T A upstream_gene_variant PACA-CA 19 59052439 59052439 single base substitution A C upstream_gene_variant PAEN-AU 19 59028615 59028615 single base substitution C T downstream_gene_variant PAEN-AU 19 59028615 59028615 single base substitution C T synonymous_variant P142P 426G>A PAEN-AU 19 59051249 59051249 single base substitution A C upstream_gene_variant PAEN-AU 19 59051998 59051998 single base substitution T G upstream_gene_variant PAEN-AU 19 59053648 59053648 single base substitution A C upstream_gene_variant PAEN-IT 19 59055013 59055013 single base substitution T C upstream_gene_variant PBCA-DE 19 59020911 59020911 single base substitution C T downstream_gene_variant PBCA-DE 19 59023529 59023529 deletion of <=200bp C - downstream_gene_variant PBCA-DE 19 59031658 59031658 single base substitution C G intron_variant PBCA-DE 19 59031658 59031658 single base substitution C G upstream_gene_variant PBCA-DE 19 59033871 59033871 single base substitution G A intron_variant PBCA-DE 19 59033871 59033871 single base substitution G A upstream_gene_variant PBCA-DE 19 59044923 59044923 deletion of <=200bp T - intron_variant PBCA-DE 19 59050414 59050414 single base substitution G A upstream_gene_variant PBCA-DE 19 59050754 59050754 insertion of <=200bp - CCT upstream_gene_variant PBCA-DE 19 59051711 59051711 insertion of <=200bp - AT upstream_gene_variant PBCA-DE 19 59052802 59052804 deletion of <=200bp CCT - upstream_gene_variant PBCA-DE 19 59053096 59053096 single base substitution C G upstream_gene_variant PBCA-DE 19 59053950 59053950 single base substitution T A upstream_gene_variant PRAD-CA 19 59046957 59046957 single base substitution G A intron_variant PRAD-UK 19 59031455 59031455 single base substitution G A 5_prime_UTR_variant PRAD-UK 19 59031455 59031455 single base substitution G A intron_variant PRAD-UK 19 59031455 59031455 single base substitution G A upstream_gene_variant PRAD-UK 19 59044143 59044143 single base substitution G A intron_variant PRAD-UK 19 59048018 59048018 insertion of <=200bp - A intron_variant PRAD-UK 19 59052424 59052424 single base substitution G C upstream_gene_variant PRAD-UK 19 59053572 59053572 single base substitution C T upstream_gene_variant PRAD-UK 19 59054070 59054070 single base substitution C G upstream_gene_variant READ-US 19 59023100 59023100 single base substitution G A downstream_gene_variant READ-US 19 59028670 59028670 single base substitution C T downstream_gene_variant READ-US 19 59028670 59028670 single base substitution C T missense_variant R124H 371G>A RECA-EU 19 59032194 59032194 single base substitution G A intron_variant RECA-EU 19 59032194 59032194 single base substitution G A upstream_gene_variant RECA-EU 19 59038281 59038281 single base substitution T A intron_variant RECA-EU 19 59043120 59043120 single base substitution G T intron_variant SKCA-BR 19 59020055 59020055 single base substitution C T downstream_gene_variant SKCA-BR 19 59020753 59020753 single base substitution G A downstream_gene_variant SKCA-BR 19 59023455 59023455 single base substitution A C downstream_gene_variant SKCA-BR 19 59029306 59029306 single base substitution G A intron_variant SKCA-BR 19 59030958 59030958 single base substitution A C intron_variant SKCA-BR 19 59030958 59030958 single base substitution A C upstream_gene_variant SKCA-BR 19 59032748 59032752 deletion of <=200bp AAAAG - intron_variant SKCA-BR 19 59032748 59032752 deletion of <=200bp AAAAG - upstream_gene_variant SKCA-BR 19 59033341 59033341 single base substitution T C intron_variant SKCA-BR 19 59033341 59033341 single base substitution T C upstream_gene_variant SKCA-BR 19 59033539 59033539 single base substitution T G intron_variant SKCA-BR 19 59033539 59033539 single base substitution T G upstream_gene_variant SKCA-BR 19 59033997 59033997 single base substitution C T intron_variant SKCA-BR 19 59033997 59033997 single base substitution C T upstream_gene_variant SKCA-BR 19 59034643 59034643 single base substitution G A intron_variant SKCA-BR 19 59034643 59034643 single base substitution G A upstream_gene_variant SKCA-BR 19 59034731 59034731 single base substitution G A intron_variant SKCA-BR 19 59034731 59034731 single base substitution G A upstream_gene_variant SKCA-BR 19 59035430 59035430 insertion of <=200bp - CA intron_variant SKCA-BR 19 59035430 59035430 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 19 59035772 59035772 single base substitution A G intron_variant SKCA-BR 19 59035772 59035772 single base substitution A G upstream_gene_variant SKCA-BR 19 59036644 59036644 single base substitution G A intron_variant SKCA-BR 19 59037877 59037877 insertion of <=200bp - GTTA intron_variant SKCA-BR 19 59037893 59037893 insertion of <=200bp - TTA intron_variant SKCA-BR 19 59037894 59037894 insertion of <=200bp - TATTA intron_variant SKCA-BR 19 59037895 59037895 single base substitution T A intron_variant SKCA-BR 19 59037898 59037898 single base substitution T A intron_variant SKCA-BR 19 59037899 59037899 single base substitution T A intron_variant SKCA-BR 19 59040047 59040047 single base substitution G A intron_variant SKCA-BR 19 59041129 59041129 single base substitution C T intron_variant SKCA-BR 19 59041724 59041724 single base substitution G A intron_variant SKCA-BR 19 59042369 59042369 single base substitution C T intron_variant SKCA-BR 19 59043575 59043575 single base substitution A G intron_variant SKCA-BR 19 59045492 59045492 single base substitution C T intron_variant SKCA-BR 19 59046508 59046508 single base substitution G A intron_variant SKCA-BR 19 59048514 59048514 single base substitution C T intron_variant SKCA-BR 19 59048640 59048640 single base substitution G A intron_variant SKCA-BR 19 59049340 59049340 single base substitution G A intron_variant SKCA-BR 19 59050414 59050414 single base substitution G A upstream_gene_variant SKCA-BR 19 59050500 59050500 single base substitution T C upstream_gene_variant SKCA-BR 19 59050543 59050543 single base substitution A C upstream_gene_variant SKCA-BR 19 59050818 59050818 single base substitution G C upstream_gene_variant SKCA-BR 19 59050967 59050967 single base substitution T C upstream_gene_variant SKCA-BR 19 59051116 59051116 single base substitution T C upstream_gene_variant SKCA-BR 19 59053950 59053950 single base substitution T A upstream_gene_variant SKCM-US 19 59022196 59022196 single base substitution G A downstream_gene_variant SKCM-US 19 59022207 59022207 single base substitution C T downstream_gene_variant SKCM-US 19 59022257 59022257 single base substitution C T downstream_gene_variant SKCM-US 19 59023011 59023011 single base substitution G A downstream_gene_variant SKCM-US 19 59025623 59025623 single base substitution T C downstream_gene_variant SKCM-US 19 59025623 59025623 single base substitution T C missense_variant Y445C 1334A>G SKCM-US 19 59028057 59028057 single base substitution G A downstream_gene_variant SKCM-US 19 59028057 59028057 single base substitution G A synonymous_variant P328P 984C>T SKCM-US 19 59028285 59028285 single base substitution C T downstream_gene_variant SKCM-US 19 59028285 59028285 single base substitution C T synonymous_variant A252A 756G>A SKCM-US 19 59028308 59028308 single base substitution G A downstream_gene_variant SKCM-US 19 59028308 59028308 single base substitution G A missense_variant L245F 733C>T SKCM-US 19 59028416 59028416 single base substitution C G downstream_gene_variant SKCM-US 19 59028416 59028416 single base substitution C G missense_variant E209Q 625G>C SKCM-US 19 59028743 59028743 single base substitution G A downstream_gene_variant SKCM-US 19 59028743 59028743 single base substitution G A synonymous_variant L100L 298C>T SKCM-US 19 59028923 59028923 single base substitution G A downstream_gene_variant SKCM-US 19 59028923 59028923 single base substitution G A missense_variant R40C 118C>T STAD-US 19 59021257 59021257 single base substitution G A downstream_gene_variant STAD-US 19 59022708 59022708 single base substitution G T downstream_gene_variant STAD-US 19 59025430 59025430 single base substitution A C downstream_gene_variant STAD-US 19 59025430 59025430 single base substitution A C synonymous_variant P509P 1527T>G STAD-US 19 59027824 59027824 single base substitution C A downstream_gene_variant STAD-US 19 59027824 59027824 single base substitution C A missense_variant S406I 1217G>T STAD-US 19 59027836 59027836 single base substitution G A downstream_gene_variant STAD-US 19 59027836 59027836 single base substitution G A missense_variant T402M 1205C>T STAD-US 19 59027859 59027859 single base substitution G A downstream_gene_variant STAD-US 19 59027859 59027859 single base substitution G A synonymous_variant R394R 1182C>T STAD-US 19 59028288 59028288 single base substitution G A downstream_gene_variant STAD-US 19 59028288 59028288 single base substitution G A synonymous_variant S251S 753C>T STAD-US 19 59028581 59028581 single base substitution G A downstream_gene_variant STAD-US 19 59028581 59028581 single base substitution G A missense_variant R154C 460C>T STAD-US 19 59028678 59028678 single base substitution A G downstream_gene_variant STAD-US 19 59028678 59028678 single base substitution A G synonymous_variant I121I 363T>C STAD-US 19 59028801 59028801 single base substitution C T downstream_gene_variant STAD-US 19 59028801 59028801 single base substitution C T synonymous_variant V80V 240G>A STAD-US 19 59028872 59028872 single base substitution A T downstream_gene_variant STAD-US 19 59028872 59028872 single base substitution A T missense_variant F57I 169T>A STAD-US 19 59028928 59028928 single base substitution C T downstream_gene_variant STAD-US 19 59028928 59028928 single base substitution C T missense_variant R38H 113G>A STAD-US 19 59028938 59028938 single base substitution C T downstream_gene_variant STAD-US 19 59028938 59028938 single base substitution C T missense_variant V35M 103G>A THCA-SA 19 59023166 59023166 single base substitution G A downstream_gene_variant THCA-SA 19 59023174 59023174 single base substitution A G downstream_gene_variant UCEC-US 19 59021365 59021365 single base substitution C T downstream_gene_variant UCEC-US 19 59021452 59021452 single base substitution A C downstream_gene_variant UCEC-US 19 59022426 59022426 single base substitution G T downstream_gene_variant UCEC-US 19 59022950 59022950 single base substitution G A downstream_gene_variant UCEC-US 19 59023537 59023537 single base substitution C T downstream_gene_variant UCEC-US 19 59027998 59027998 single base substitution G A downstream_gene_variant UCEC-US 19 59027998 59027998 single base substitution G A missense_variant A348V 1043C>T UCEC-US 19 59028407 59028407 single base substitution C T downstream_gene_variant UCEC-US 19 59028407 59028407 single base substitution C T missense_variant E212K 634G>A UCEC-US 19 59028424 59028424 single base substitution C T downstream_gene_variant UCEC-US 19 59028424 59028424 single base substitution C T missense_variant R206Q 617G>A UCEC-US 19 59028440 59028440 single base substitution C T downstream_gene_variant UCEC-US 19 59028440 59028440 single base substitution C T missense_variant A201T 601G>A UCEC-US 19 59028960 59028960 single base substitution C A downstream_gene_variant UCEC-US 19 59028960 59028960 single base substitution C A missense_variant R27S 81G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LUAD-S01357 COSM386998 c.605C>A p.A202D Substitution - Missense 19:58517069-58517069 - TCGA-DK-A3IL-01 COSM1305242 c.555A>G p.P185P Substitution - coding silent 19:58517119-58517119 - TP_2010 COSM5564729 c.520C>T p.R174C Substitution - Missense 19:58517154-58517154 - I2L-P28-Tumor-Biopsy COSM5365417 c.114C>T p.R38R Substitution - coding silent 19:58517560-58517560 - ESO-114 COSM1270725 c.1241C>T p.S414F Substitution - Missense 19:58516433-58516433 - TCGA-AP-A0LF-01 COSM1002772 c.328C>T p.R110C Substitution - Missense 19:58517346-58517346 - TCGA-EK-A3GK-01 COSM4853170 c.1341C>G p.L447L Substitution - coding silent 19:58514249-58514249 - PD4137a COSM165670 c.200C>T p.S67F Substitution - Missense 19:58517474-58517474 - OSCC-GB_00250111 COSM3713074 c.1392C>A p.C464* Substitution - Nonsense 19:58514198-58514198 - STC263 COSM5057041 c.660C>T p.G220G Substitution - coding silent 19:58517014-58517014 - TCGA-BR-7707-01 COSM4082470 c.113G>A p.R38H Substitution - Missense 19:58517561-58517561 - LUAD-B01169 COSM333604 c.487G>T p.G163W Substitution - Missense 19:58517187-58517187 - HCC2 COSM1613009 c.646G>T p.D216Y Substitution - Missense 19:58517028-58517028 - TCGA-BR-4370-01 COSM4082461 c.753C>T p.S251S Substitution - coding silent 19:58516921-58516921 - T1772 COSM4742185 c.770_771insC p.A258fs*7 Insertion - Frameshift 19:58516903-58516904 - TCGA-BG-A0LX-01 COSM1002771 c.601G>A p.A201T Substitution - Missense 19:58517073-58517073 - TCGA-CU-A3YL-01 COSM3797646 c.412A>C p.T138P Substitution - Missense 19:58517262-58517262 - PTC-77C COSM4132712 c.456C>T p.R152R Substitution - coding silent 19:58517218-58517218 - B105-1-Tumor COSM1751230 c.584C>T p.A195V Substitution - Missense 19:58517090-58517090 - TCGA-G7-6790-01 COSM3990372 c.1210G>C p.E404Q Substitution - Missense 19:58516464-58516464 - TCGA-60-2722-01 COSM714036 c.671A>T p.E224V Substitution - Missense 19:58517003-58517003 - T3118 COSM4742183 c.805G>T p.G269W Substitution - Missense 19:58516869-58516869 - 131169 COSM1645132 c.1412A>G p.K471R Substitution - Missense 19:58514178-58514178 - TCGA-HP-A5MZ-01 COSM2974748 c.5C>T p.A2V Substitution - Missense 19:58517669-58517669 - TCGA-D3-A1QA-06 COSM3540818 c.625G>C p.E209Q Substitution - Missense 19:58517049-58517049 - B105-1 COSM1751230 c.584C>T p.A195V Substitution - Missense 19:58517090-58517090 - TCGA-A6-6780-01 COSM1397348 c.1201C>T p.P401S Substitution - Missense 19:58516473-58516473 - TCGA-EE-A181-06 COSM3540816 c.733C>T p.L245F Substitution - Missense 19:58516941-58516941 - ESO-859 COSM1240687 c.748G>A p.D250N Substitution - Missense 19:58516926-58516926 - LP6005409-DNA_F02 COSM4408732 c.49C>T p.R17C Substitution - Missense 19:58517625-58517625 - TCGA-D3-A2JF-06 COSM3540810 c.1334A>G p.Y445C Substitution - Missense 19:58514256-58514256 - TCGA-G2-A2EO-01 COSM1305241 c.1413G>A p.K471K Substitution - coding silent 19:58514177-58514177 - T154 COSM1177625 c.614A>T p.D205V Substitution - Missense 19:58517060-58517060 - Pat_41_A COSM2974719 c.616C>T p.R206* Substitution - Nonsense 19:58517058-58517058 - CSCC-16-T COSM4559487 c.806G>A p.G269E Substitution - Missense 19:58516868-58516868 - TCGA-BR-4363-01 COSM4082468 c.169T>A p.F57I Substitution - Missense 19:58517505-58517505 - HX13T COSM1613010 c.348C>T p.D116D Substitution - coding silent 19:58517326-58517326 - Pat_41_B COSM5856992 c.740C>T p.A247V Substitution - Missense 19:58516934-58516934 - 587328 COSM1233155 c.1350G>C p.M450I Substitution - Missense 19:58514240-58514240 - TCGA-DB-A64L-01 COSM3971325 c.670G>A p.E224K Substitution - Missense 19:58517004-58517004 - PD7243a COSM5000382 c.370C>T p.R124C Substitution - Missense 19:58517304-58517304 - TCGA-EE-A29E-06 COSM3540822 c.118C>T p.R40C Substitution - Missense 19:58517556-58517556 - HCT-116 COSM1684602 c.1481_1483delTCT p.F495delF Deletion - In frame 19:58514107-58514109 - TCGA-AP-A059-01 COSM1002768 c.1043C>T p.A348V Substitution - Missense 19:58516631-58516631 - TCGA-AC-A23H-01 COSM1002772 c.328C>T p.R110C Substitution - Missense 19:58517346-58517346 - 345973 COSM1002772 c.328C>T p.R110C Substitution - Missense 19:58517346-58517346 - HCC160 COSM3707492 c.788C>T p.A263V Substitution - Missense 19:58516886-58516886 - TCGA-AZ-6598-01 COSM1397347 c.1244G>A p.R415Q Substitution - Missense 19:58516430-58516430 - HCC2T COSM1613009 c.646G>T p.D216Y Substitution - Missense 19:58517028-58517028 - TCGA-BR-4368-01 COSM4082453 c.1527T>G p.P509P Substitution - coding silent 19:58514063-58514063 - B89-5-Tumor COSM1751231 c.14A>C p.E5A Substitution - Missense 19:58517660-58517660 - HCC160T COSM3707492 c.788C>T p.A263V Substitution - Missense 19:58516886-58516886 - PTC-70C COSM4132708 c.677G>A p.G226D Substitution - Missense 19:58516997-58516997 - LP6005334-DNA_C02 COSM4412468 c.1049C>T p.S350L Substitution - Missense 19:58516625-58516625 - PTC-53C COSM4132710 c.510C>A p.S170R Substitution - Missense 19:58517164-58517164 - TCGA-D1-A0ZR-01 COSM1002769 c.634G>A p.E212K Substitution - Missense 19:58517040-58517040 - TCGA-EI-6882-01 COSM3423325 c.371G>A p.R124H Substitution - Missense 19:58517303-58517303 - L363 COSM1235952 c.976G>A p.G326R Substitution - Missense 19:58516698-58516698 - PT23_1 COSM5903234 c.527C>T p.P176L Substitution - Missense 19:58517147-58517147 - EGC15 COSM5057039 c.1379A>G p.Q460R Substitution - Missense 19:58514211-58514211 - HCC4T COSM1613010 c.348C>T p.D116D Substitution - coding silent 19:58517326-58517326 - PCSI_0476_Pa_P_526 COSM5031447 c.1477A>C p.K493Q Substitution - Missense 19:58514113-58514113 - TCGA-EE-A29L-06 COSM3540812 c.984C>T p.P328P Substitution - coding silent 19:58516690-58516690 - CSCC-56-T COSM4513851 c.952C>T p.R318C Substitution - Missense 19:58516722-58516722 - TCGA-ER-A197-06 COSM3540814 c.756G>A p.A252A Substitution - coding silent 19:58516918-58516918 - T3152 COSM4082461 c.753C>T p.S251S Substitution - coding silent 19:58516921-58516921 - TCGA-BR-4201-01 COSM4082466 c.240G>A p.V80V Substitution - coding silent 19:58517434-58517434 - B89-5 COSM1751231 c.14A>C p.E5A Substitution - Missense 19:58517660-58517660 - 08-P462 COSM2974718 c.624C>T p.D208D Substitution - coding silent 19:58517050-58517050 - ESO-081 COSM1243748 c.86G>T p.G29V Substitution - Missense 19:58517588-58517588 - TCGA-IR-A3LB-01 COSM4829391 c.1277C>T p.S426L Substitution - Missense 19:58516397-58516397 - BK0017 COSM4186051 c.226C>T p.P76S Substitution - Missense 19:58517448-58517448 - PDA_044 COSM5000382 c.370C>T p.R124C Substitution - Missense 19:58517304-58517304 - PD5122a COSM3719616 c.674G>A p.G225D Substitution - Missense 19:58517000-58517000 - T3021 COSM4742191 c.440C>T p.A147V Substitution - Missense 19:58517234-58517234 - 25T COSM3713074 c.1392C>A p.C464* Substitution - Nonsense 19:58514198-58514198 - TCGA-BR-8382-01 COSM4082459 c.1182C>T p.R394R Substitution - coding silent 19:58516492-58516492 - TCGA-FG-7641-01 COSM3971327 c.117T>G p.I39M Substitution - Missense 19:58517557-58517557 - LP6005409-DNA_A02 COSM4409733 c.749A>T p.D250V Substitution - Missense 19:58516925-58516925 - TCGA-BR-8360-01 COSM4082472 c.103G>A p.V35M Substitution - Missense 19:58517571-58517571 - TCGA-AP-A059-01 COSM1002773 c.81G>T p.R27S Substitution - Missense 19:58517593-58517593 - LUAD-LC15C COSM341802 c.486G>A p.P162P Substitution - coding silent 19:58517188-58517188 - XHDG04 COSM4768375 c.1350G>A p.M450I Substitution - Missense 19:58514240-58514240 - HCC4 COSM1613010 c.348C>T p.D116D Substitution - coding silent 19:58517326-58517326 - TCGA-FD-A3B4-01 COSM1305240 c.1450G>A p.E484K Substitution - Missense 19:58514140-58514140 - T636 COSM4742193 c.133C>T p.R45C Substitution - Missense 19:58517541-58517541 - TCGA-GF-A3OT-06 COSM3540820 c.298C>T p.L100L Substitution - coding silent 19:58517376-58517376 - T3535 COSM2974739 c.231G>A p.A77A Substitution - coding silent 19:58517443-58517443 - TCGA-AA-3697-01 COSM3693166 c.369C>T p.A123A Substitution - coding silent 19:58517305-58517305 - PD4105a COSM165669 c.160G>A p.G54S Substitution - Missense 19:58517514-58517514 - TCGA-CD-8536-01 COSM4082457 c.1205C>T p.T402M Substitution - Missense 19:58516469-58516469 - T3021 COSM4742187 c.600C>T p.S200S Substitution - coding silent 19:58517074-58517074 - TCGA-CK-5913-01 COSM1397349 c.870T>C p.T290T Substitution - coding silent 19:58516804-58516804 - TCGA-D7-A4YY-01 COSM4082464 c.363T>C p.I121I Substitution - coding silent 19:58517311-58517311 - ESO-859 COSM1240688 c.1275C>T p.H425H Substitution - coding silent 19:58516399-58516399 - 8031157 COSM4138267 c.426G>A p.P142P Substitution - coding silent 19:58517248-58517248 - PD24182a COSM5790876 c.10G>A p.A4T Substitution - Missense 19:58517664-58517664 - T1154 COSM4742189 c.531G>A p.A177A Substitution - coding silent 19:58517143-58517143 - TCGA-BR-6852-01 COSM2974727 c.460C>T p.R154C Substitution - Missense 19:58517214-58517214 - TCGA-HU-A4GU-01 COSM4082455 c.1217G>T p.S406I Substitution - Missense 19:58516457-58516457 - PCSI_0476_Pa_P_526 COSM5031380 c.1479G>A p.K493K Substitution - coding silent 19:58514111-58514111 - QC2-36-T2 COSM5655341 c.161G>T p.G54V Substitution - Missense 19:58517513-58517513 - STC252 COSM1002771 c.601G>A p.A201T Substitution - Missense 19:58517073-58517073 - TCGA-DK-A1AB-01 COSM418734 c.688G>A p.E230K Substitution - Missense 19:58516986-58516986 - 93VU147T COSM4408732 c.49C>T p.R17C Substitution - Missense 19:58517625-58517625 - TCGA-BS-A0UV-01 COSM1002770 c.617G>A p.R206Q Substitution - Missense 19:58517057-58517057 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.515662 19q13.43

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.I39M c.117T>G 19 59028924 LGG A C Synonymous p.P509P c.1527T>G 19 59025430 STAD A T Missense p.F57I c.169T>A 19 59028872 STAD C A Missense p.G163W c.487G>T 19 59028554 LUAD C G Missense p.E209Q c.625G>C 19 59028416 CM C T Missense p.A201T c.601G>A 19 59028440 UCEC C T Missense p.D219N c.655G>A 19 59028386 HNSC C T Missense p.D250N c.748G>A 19 59028293 ESCA C T Missense p.E212K c.634G>A 19 59028407 UCEC C T Missense p.E217K c.649G>A 19 59028392 LUAD C T Missense p.E230K c.688G>A 19 59028353 BLCA C T Missense p.E484K c.1450G>A 19 59025507 BLCA C T Missense p.G54S c.160G>A 19 59028881 BRCA C T Missense p.R17H c.50G>A 19 59028991 HNSC C T Synonymous p.A252A c.756G>A 19 59028285 CM C T Synonymous p.P142P c.426G>A 19 59028615 HNSC C T Synonymous p.P327P c.981G>A 19 59028060 HNSC C T Synonymous p.V80V c.240G>A 19 59028801 STAD G A Missense p.L245F c.733C>T 19 59028308 CM G A Missense p.R154C c.460C>T 19 59028581 STAD G A Missense p.S131F c.392C>T 19 59028649 LUAD G A Missense p.S414F c.1241C>T 19 59027800 ESCA G A Missense p.S67F c.200C>T 19 59028841 BRCA G A Synonymous p.H425H c.1275C>T 19 59027766 ESCA G A Synonymous p.P328P c.984C>T 19 59028057 CM G A Synonymous p.S251S c.753C>T 19 59028288 STAD G T Missense p.H421Q c.1263C>A 19 59027778 LUAD T A Missense p.E224V c.671A>T 19 59028370 LUSC T C Missense p.Y445C c.1334A>G 19 59025623 CM T C Synonymous p.P185P c.555A>G 19 59028486 BLCA