Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 19 18778894 18778894 + Silent SNP G G A TCGA-GV-A3JW-01A-11D-A20D-08 TCGA-GV-A3JW-10A-01D-A20D-08 g.chr19:18778894G>A c.687G>A c.(685-687)gcG>gcA p.A229A BLCA 19 18779024 18779024 + Missense_Mutation SNP G G A TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr19:18779024G>A c.817G>A c.(817-819)Gag>Aag p.E273K BLCA 19 18779242 18779242 + Silent SNP G G A TCGA-GV-A40G-01A-11D-A23M-08 TCGA-GV-A40G-10A-01D-A23K-08 g.chr19:18779242G>A c.1035G>A c.(1033-1035)acG>acA p.T345T BLCA 19 18779479 18779479 + Silent SNP C C T TCGA-E7-A5KE-01A-11D-A289-08 TCGA-E7-A5KE-10A-01D-A289-08 g.chr19:18779479C>T c.1272C>T c.(1270-1272)gcC>gcT p.A424A BRCA 19 18779780 18779780 + Missense_Mutation SNP G G A TCGA-GM-A2DF-01A-11D-A17W-09 TCGA-GM-A2DF-10C-01D-A17W-09 g.chr19:18779780G>A c.1573G>A c.(1573-1575)Gac>Aac p.D525N BRCA 19 18779977 18779977 + Silent SNP G G A TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr19:18779977G>A c.1770G>A c.(1768-1770)cgG>cgA p.R590R COAD 19 18775147 18775147 + Missense_Mutation SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr19:18775147G>A c.160G>A c.(160-162)Gcc>Acc p.A54T COAD 19 18778502 18778502 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr19:18778502G>T c.295G>T c.(295-297)Gca>Tca p.A99S COAD 19 18778748 18778748 + Nonsense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr19:18778748C>T c.541C>T c.(541-543)Cga>Tga p.R181* COAD 19 18778830 18778830 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr19:18778830G>A c.623G>A c.(622-624)cGc>cAc p.R208H COAD 19 18779306 18779306 + Frame_Shift_Del DEL G G - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr19:18779306delG c.1099delG c.(1099-1101)gggfs p.G368fs COADREAD 19 18775147 18775147 + Missense_Mutation SNP G G A TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr19:18775147G>A c.160G>A c.(160-162)Gcc>Acc p.A54T COADREAD 19 18778502 18778502 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr19:18778502G>T c.295G>T c.(295-297)Gca>Tca p.A99S COADREAD 19 18778748 18778748 + Nonsense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr19:18778748C>T c.541C>T c.(541-543)Cga>Tga p.R181* COADREAD 19 18778830 18778830 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr19:18778830G>A c.623G>A c.(622-624)cGc>cAc p.R208H COADREAD 19 18779181 18779181 + Missense_Mutation SNP C C T TCGA-AF-2693-01A-02D-1733-10 TCGA-AF-2693-10A-01D-1733-10 g.chr19:18779181C>T c.974C>T c.(973-975)tCg>tTg p.S325L COADREAD 19 18779306 18779306 + Frame_Shift_Del DEL G G - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr19:18779306delG c.1099delG c.(1099-1101)gggfs p.G368fs DLBC 19 18778879 18778879 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr19:18778879C>T c.672C>T c.(670-672)atC>atT p.I224I DLBC 19 18779113 18779113 + Silent SNP C C T TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr19:18779113C>T c.906C>T c.(904-906)acC>acT p.T302T DLBC 19 18779728 18779728 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr19:18779728C>T c.1521C>T c.(1519-1521)ggC>ggT p.G507G ESCA 19 18775251 18775251 + Missense_Mutation SNP C C A TCGA-L5-A4OS-01A-11D-A28B-09 TCGA-L5-A4OS-11A-11D-A28E-09 g.chr19:18775251C>A c.264C>A c.(262-264)ttC>ttA p.F88L ESCA 19 18779956 18779956 + Silent SNP G G A TCGA-2H-A9GO-01A-11D-A37C-09 TCGA-2H-A9GO-11A-11D-A37F-09 g.chr19:18779956G>A c.1749G>A c.(1747-1749)acG>acA p.T583T ESCA 19 18779978 18779978 + Missense_Mutation SNP G G A TCGA-IG-A3I8-01A-11D-A247-09 TCGA-IG-A3I8-10A-01D-A247-09 g.chr19:18779978G>A c.1771G>A c.(1771-1773)Gac>Aac p.D591N GBM 19 18779533 18779533 + Silent SNP C C T TCGA-06-0122-01A-01D-1490-08 TCGA-06-0122-10A-01D-1490-08 g.chr19:18779533C>T c.1326C>T c.(1324-1326)taC>taT p.Y442Y GBMLGG 19 18775153 18775153 + Missense_Mutation SNP C C T TCGA-DU-A6S8-01A-12D-A32B-08 TCGA-DU-A6S8-10A-01D-A329-08 g.chr19:18775153C>T c.166C>T c.(166-168)Ctc>Ttc p.L56F GBMLGG 19 18779269 18779269 + Silent SNP G G A TCGA-EZ-7264-01A-11D-2024-08 TCGA-EZ-7264-10A-01D-2024-08 g.chr19:18779269G>A c.1062G>A c.(1060-1062)acG>acA p.T354T GBMLGG 19 18779533 18779533 + Silent SNP C C T TCGA-06-0122-01A-01D-1490-08 TCGA-06-0122-10A-01D-1490-08 g.chr19:18779533C>T c.1326C>T c.(1324-1326)taC>taT p.Y442Y HNSC 19 18775082 18775082 + Missense_Mutation SNP A A G TCGA-CQ-A4CG-01A-11D-A25Y-08 TCGA-CQ-A4CG-10A-01D-A25Y-08 g.chr19:18775082A>G c.95A>G c.(94-96)aAg>aGg p.K32R HNSC 19 18778789 18778789 + Missense_Mutation SNP G G C TCGA-CV-7102-01A-11D-2012-08 TCGA-CV-7102-10A-01D-2013-08 g.chr19:18778789G>C c.582G>C c.(580-582)caG>caC p.Q194H HNSC 19 18779586 18779586 + Missense_Mutation SNP G G T TCGA-BA-5556-01A-01D-1512-08 TCGA-BA-5556-10A-01D-1512-08 g.chr19:18779586G>T c.1379G>T c.(1378-1380)gGc>gTc p.G460V HNSC 19 18779737 18779737 + Silent SNP C C T TCGA-CV-A6JM-01A-11D-A31L-08 TCGA-CV-A6JM-10A-01D-A31J-08 g.chr19:18779737C>T c.1530C>T c.(1528-1530)atC>atT p.I510I KIPAN 19 18778568 18778568 + Missense_Mutation SNP G G A TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr19:18778568G>A c.361G>A c.(361-363)Gcc>Acc p.A121T KIPAN 19 18778755 18778755 + Missense_Mutation SNP C C G TCGA-BP-5195-01A-02D-1429-08 TCGA-BP-5195-11A-01D-1429-08 g.chr19:18778755C>G c.548C>G c.(547-549)tCg>tGg p.S183W KIRC 19 18778755 18778755 + Missense_Mutation SNP C C G TCGA-BP-5195-01A-02D-1429-08 TCGA-BP-5195-11A-01D-1429-08 g.chr19:18778755C>G c.548C>G c.(547-549)tCg>tGg p.S183W KIRP 19 18778568 18778568 + Missense_Mutation SNP G G A TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr19:18778568G>A c.361G>A c.(361-363)Gcc>Acc p.A121T LGG 19 18775153 18775153 + Missense_Mutation SNP C C T TCGA-DU-A6S8-01A-12D-A32B-08 TCGA-DU-A6S8-10A-01D-A329-08 g.chr19:18775153C>T c.166C>T c.(166-168)Ctc>Ttc p.L56F LGG 19 18779269 18779269 + Silent SNP G G A TCGA-EZ-7264-01A-11D-2024-08 TCGA-EZ-7264-10A-01D-2024-08 g.chr19:18779269G>A c.1062G>A c.(1060-1062)acG>acA p.T354T LIHC 19 18778935 18778935 + Missense_Mutation SNP G G T TCGA-DD-AADP-01A-11D-A38X-10 TCGA-DD-AADP-10A-01D-A38X-10 g.chr19:18778935G>T c.728G>T c.(727-729)cGc>cTc p.R243L LUAD 19 18775203 18775203 + Missense_Mutation SNP G G T TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr19:18775203G>T c.216G>T c.(214-216)gaG>gaT p.E72D LUAD 19 18778558 18778558 + Missense_Mutation SNP C C G TCGA-50-5931-01A-11D-1753-08 TCGA-50-5931-11A-01D-1753-08 g.chr19:18778558C>G c.351C>G c.(349-351)atC>atG p.I117M LUAD 19 18778620 18778620 + Missense_Mutation SNP G G A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr19:18778620G>A c.413G>A c.(412-414)gGc>gAc p.G138D LUAD 19 18778916 18778916 + Missense_Mutation SNP G G T TCGA-49-4488-01A-01D-1753-08 TCGA-49-4488-11A-01D-1753-08 g.chr19:18778916G>T c.709G>T c.(709-711)Gac>Tac p.D237Y LUAD 19 18779362 18779362 + Silent SNP C C T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr19:18779362C>T c.1155C>T c.(1153-1155)cgC>cgT p.R385R LUAD 19 18779735 18779735 + Missense_Mutation SNP A A G TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr19:18779735A>G c.1528A>G c.(1528-1530)Atc>Gtc p.I510V LUAD 19 18779844 18779844 + Missense_Mutation SNP G G A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr19:18779844G>A c.1637G>A c.(1636-1638)cGg>cAg p.R546Q LUSC 19 18778613 18778613 + Missense_Mutation SNP G G T TCGA-39-5016-01A-01D-1441-08 TCGA-39-5016-11A-01D-1441-08 g.chr19:18778613G>T c.406G>T c.(406-408)Gtg>Ttg p.V136L LUSC 19 18778681 18778681 + Silent SNP G G A TCGA-66-2742-01A-01D-0983-08 TCGA-66-2742-11A-01D-0983-08 g.chr19:18778681G>A c.474G>A c.(472-474)gcG>gcA p.A158A LUSC 19 18778777 18778777 + Silent SNP G G C TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr19:18778777G>C c.570G>C c.(568-570)cgG>cgC p.R190R LUSC 19 18779381 18779381 + Missense_Mutation SNP C C T TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr19:18779381C>T c.1174C>T c.(1174-1176)Cgc>Tgc p.R392C LUSC 19 18779702 18779702 + Missense_Mutation SNP G G A TCGA-34-5927-01A-11D-1817-08 TCGA-34-5927-10A-01D-1817-08 g.chr19:18779702G>A c.1495G>A c.(1495-1497)Gtg>Atg p.V499M OV 19 18779040 18779040 + Missense_Mutation SNP G G A TCGA-13-1509-01A-01W-0549-09 TCGA-13-1509-10A-01W-0550-09 g.chr19:18779040G>A c.833G>A c.(832-834)cGc>cAc p.R278H PAAD 19 18778902 18778902 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:18778902G>A c.695G>A c.(694-696)cGc>cAc p.R232H PAAD 19 18779455 18779455 + Silent SNP C C T TCGA-2L-AAQA-01A-21D-A38G-08 TCGA-2L-AAQA-11A-11D-A38J-08 g.chr19:18779455C>T c.1248C>T c.(1246-1248)taC>taT p.Y416Y PAAD 19 18779809 18779809 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:18779809G>A c.1602G>A c.(1600-1602)ccG>ccA p.P534P PRAD 19 18775073 18775073 + Missense_Mutation SNP C C T TCGA-ZG-A9N3-01A-11D-A41K-08 TCGA-ZG-A9N3-10A-01D-A41N-08 g.chr19:18775073C>T c.86C>T c.(85-87)aCg>aTg p.T29M PRAD 19 18778497 18778497 + Missense_Mutation SNP G G A TCGA-EJ-7791-01A-11D-2114-08 TCGA-EJ-7791-10A-01D-2115-08 g.chr19:18778497G>A c.290G>A c.(289-291)cGg>cAg p.R97Q PRAD 19 18778931 18778931 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:18778931C>T c.724C>T c.(724-726)Ccg>Tcg p.P242S PRAD 19 18779107 18779107 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:18779107G>A c.900G>A c.(898-900)ccG>ccA p.P300P READ 19 18779181 18779181 + Missense_Mutation SNP C C T TCGA-AF-2693-01A-02D-1733-10 TCGA-AF-2693-10A-01D-1733-10 g.chr19:18779181C>T c.974C>T c.(973-975)tCg>tTg p.S325L SARC 19 18775148 18775148 + Missense_Mutation SNP C C T TCGA-3B-A9I1-01A-11D-A38Z-09 TCGA-3B-A9I1-10A-01D-A38Z-09 g.chr19:18775148C>T c.161C>T c.(160-162)gCc>gTc p.A54V SKCM 19 18775173 18775173 + Silent SNP C C T TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr19:18775173C>T c.186C>T c.(184-186)ctC>ctT p.L62L SKCM 19 18775198 18775198 + Missense_Mutation SNP A A G TCGA-ER-A19J-06A-11D-A196-08 TCGA-ER-A19J-10A-01D-A198-08 g.chr19:18775198A>G c.211A>G c.(211-213)Aga>Gga p.R71G SKCM 19 18775224 18775224 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:18775224C>T c.237C>T c.(235-237)gtC>gtT p.V79V SKCM 19 18778511 18778511 + Missense_Mutation SNP G G A TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr19:18778511G>A c.304G>A c.(304-306)Gac>Aac p.D102N SKCM 19 18778631 18778631 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr19:18778631T>G c.424T>G c.(424-426)Ttc>Gtc p.F142V SKCM 19 18778810 18778810 + Silent SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr19:18778810C>T c.603C>T c.(601-603)ttC>ttT p.F201F SKCM 19 18779140 18779140 + Silent SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr19:18779140C>T c.933C>T c.(931-933)ctC>ctT p.L311L SKCM 19 18779689 18779689 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr19:18779689G>A c.1482G>A c.(1480-1482)atG>atA p.M494I SKCM 19 18779856 18779856 + Missense_Mutation SNP C C T TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr19:18779856C>T c.1649C>T c.(1648-1650)tCa>tTa p.S550L SKCM 19 18779932 18779932 + Silent SNP G G A TCGA-FR-A44A-06A-11D-A24R-08 TCGA-FR-A44A-10A-01D-A24R-08 g.chr19:18779932G>A c.1725G>A c.(1723-1725)acG>acA p.T575T SKCM 19 18779933 18779933 + Missense_Mutation SNP G G A TCGA-FR-A44A-06A-11D-A24R-08 TCGA-FR-A44A-10A-01D-A24R-08 g.chr19:18779933G>A c.1726G>A c.(1726-1728)Ggc>Agc p.G576S

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 18778633 18778633 single base substitution C T 3_prime_UTR_variant BLCA-CN 19 18778633 18778633 single base substitution C T downstream_gene_variant BLCA-CN 19 18778633 18778633 single base substitution C T exon_variant BLCA-CN 19 18778633 18778633 single base substitution C T intron_variant BLCA-CN 19 18778633 18778633 single base substitution C T synonymous_variant F142F 426C>T BLCA-CN 19 18778633 18778633 single base substitution C T synonymous_variant F170F 510C>T BLCA-CN 19 18778837 18778837 single base substitution C G downstream_gene_variant BLCA-CN 19 18778837 18778837 single base substitution C G intron_variant BLCA-CN 19 18778837 18778837 single base substitution C G synonymous_variant V210V 630C>G BLCA-CN 19 18779183 18779183 single base substitution G T downstream_gene_variant BLCA-CN 19 18779183 18779183 single base substitution G T intron_variant BLCA-CN 19 18779183 18779183 single base substitution G T missense_variant V326F 976G>T BLCA-US 19 18778894 18778894 single base substitution G A downstream_gene_variant BLCA-US 19 18778894 18778894 single base substitution G A intron_variant BLCA-US 19 18778894 18778894 single base substitution G A synonymous_variant A229A 687G>A BLCA-US 19 18779242 18779242 single base substitution G A downstream_gene_variant BLCA-US 19 18779242 18779242 single base substitution G A intron_variant BLCA-US 19 18779242 18779242 single base substitution G A synonymous_variant T345T 1035G>A BOCA-FR 19 18746735 18746735 single base substitution G T upstream_gene_variant BOCA-FR 19 18774002 18774002 single base substitution C T intron_variant BRCA-EU 19 18743038 18743038 single base substitution G A upstream_gene_variant BRCA-EU 19 18743658 18743658 single base substitution G C upstream_gene_variant BRCA-EU 19 18749642 18749642 single base substitution C T intron_variant BRCA-EU 19 18751054 18751054 insertion of <=200bp - T intron_variant BRCA-EU 19 18751054 18751054 insertion of <=200bp - T upstream_gene_variant BRCA-EU 19 18754753 18754753 single base substitution C T intron_variant BRCA-EU 19 18754753 18754753 single base substitution C T upstream_gene_variant BRCA-EU 19 18755512 18755512 single base substitution T C intron_variant BRCA-EU 19 18756031 18756031 single base substitution T C intron_variant BRCA-EU 19 18757715 18757715 single base substitution G C intron_variant BRCA-EU 19 18758513 18758513 single base substitution G A intron_variant BRCA-EU 19 18758698 18758698 single base substitution C G intron_variant BRCA-EU 19 18758930 18758930 single base substitution G T intron_variant BRCA-EU 19 18759704 18759704 single base substitution A T intron_variant BRCA-EU 19 18761859 18761859 single base substitution G C intron_variant BRCA-EU 19 18761890 18761890 single base substitution T G intron_variant BRCA-EU 19 18761969 18761969 single base substitution T C intron_variant BRCA-EU 19 18762244 18762244 single base substitution T C intron_variant BRCA-EU 19 18764011 18764011 single base substitution G T intron_variant BRCA-EU 19 18766352 18766352 single base substitution G A intron_variant BRCA-EU 19 18766823 18766823 single base substitution C T intron_variant BRCA-EU 19 18766949 18766949 single base substitution G C intron_variant BRCA-EU 19 18768522 18768522 single base substitution C G intron_variant BRCA-EU 19 18769989 18769989 single base substitution A T intron_variant BRCA-EU 19 18770667 18770667 single base substitution C T intron_variant BRCA-EU 19 18771331 18771331 single base substitution G A intron_variant BRCA-EU 19 18771655 18771655 single base substitution C T intron_variant BRCA-EU 19 18772880 18772880 single base substitution T C intron_variant BRCA-EU 19 18780897 18780897 single base substitution C T 3_prime_UTR_variant BRCA-EU 19 18780897 18780897 single base substitution C T downstream_gene_variant BRCA-EU 19 18782116 18782116 single base substitution A C downstream_gene_variant BRCA-EU 19 18782287 18782287 single base substitution C T downstream_gene_variant BRCA-FR 19 18758698 18758698 single base substitution C G intron_variant BRCA-FR 19 18780897 18780897 single base substitution C T 3_prime_UTR_variant BRCA-FR 19 18780897 18780897 single base substitution C T downstream_gene_variant BRCA-FR 19 18780974 18780974 single base substitution C A 3_prime_UTR_variant BRCA-FR 19 18780974 18780974 single base substitution C A downstream_gene_variant BRCA-UK 19 18746870 18746870 single base substitution C T upstream_gene_variant BRCA-UK 19 18778675 18778675 single base substitution G A downstream_gene_variant BRCA-UK 19 18778675 18778675 single base substitution G A exon_variant BRCA-UK 19 18778675 18778675 single base substitution G A intron_variant BRCA-UK 19 18778675 18778675 single base substitution G A synonymous_variant L156L 468G>A BRCA-UK 19 18778675 18778675 single base substitution G A synonymous_variant L184L 552G>A BRCA-UK 19 18780253 18780253 single base substitution G A 3_prime_UTR_variant BRCA-UK 19 18780253 18780253 single base substitution G A downstream_gene_variant BRCA-US 19 18779780 18779780 single base substitution G A downstream_gene_variant BRCA-US 19 18779780 18779780 single base substitution G A intron_variant BRCA-US 19 18779780 18779780 single base substitution G A missense_variant D525N 1573G>A BRCA-US 19 18779977 18779977 single base substitution G A downstream_gene_variant BRCA-US 19 18779977 18779977 single base substitution G A intron_variant BRCA-US 19 18779977 18779977 single base substitution G A synonymous_variant R590R 1770G>A BTCA-JP 19 18779542 18779542 single base substitution G A downstream_gene_variant BTCA-JP 19 18779542 18779542 single base substitution G A intron_variant BTCA-JP 19 18779542 18779542 single base substitution G A synonymous_variant S445S 1335G>A BTCA-JP 19 18779939 18779939 single base substitution G A downstream_gene_variant BTCA-JP 19 18779939 18779939 single base substitution G A intron_variant BTCA-JP 19 18779939 18779939 single base substitution G A missense_variant V578I 1732G>A CLLE-ES 19 18765285 18765285 single base substitution G A intron_variant CLLE-ES 19 18770523 18770523 single base substitution C A exon_variant CLLE-ES 19 18770523 18770523 single base substitution C A intron_variant COAD-US 19 18775070 18775070 single base substitution G A splice_acceptor_variant COAD-US 19 18775077 18775077 single base substitution C T 3_prime_UTR_variant COAD-US 19 18775077 18775077 single base substitution C T exon_variant COAD-US 19 18775077 18775077 single base substitution C T synonymous_variant A29A 87C>T COAD-US 19 18775077 18775077 single base substitution C T synonymous_variant A30A 90C>T COAD-US 19 18775147 18775147 single base substitution G A 3_prime_UTR_variant COAD-US 19 18775147 18775147 single base substitution G A exon_variant COAD-US 19 18775147 18775147 single base substitution G A missense_variant A53T 157G>A COAD-US 19 18775147 18775147 single base substitution G A missense_variant A54T 160G>A COAD-US 19 18778502 18778502 single base substitution G T 3_prime_UTR_variant COAD-US 19 18778502 18778502 single base substitution G T downstream_gene_variant COAD-US 19 18778502 18778502 single base substitution G T exon_variant COAD-US 19 18778502 18778502 single base substitution G T missense_variant A127S 379G>T COAD-US 19 18778502 18778502 single base substitution G T missense_variant A99S 295G>T COAD-US 19 18778830 18778830 single base substitution G A downstream_gene_variant COAD-US 19 18778830 18778830 single base substitution G A intron_variant COAD-US 19 18778830 18778830 single base substitution G A missense_variant R208H 623G>A COAD-US 19 18779306 18779306 deletion of <=200bp G - downstream_gene_variant COAD-US 19 18779306 18779306 deletion of <=200bp G - frameshift_variant G367 COAD-US 19 18779306 18779306 deletion of <=200bp G - intron_variant COAD-US 19 18779514 18779514 single base substitution G A downstream_gene_variant COAD-US 19 18779514 18779514 single base substitution G A intron_variant COAD-US 19 18779514 18779514 single base substitution G A missense_variant R436Q 1307G>A COCA-CN 19 18778479 18778479 single base substitution T C 3_prime_UTR_variant COCA-CN 19 18778479 18778479 single base substitution T C downstream_gene_variant COCA-CN 19 18778479 18778479 single base substitution T C exon_variant COCA-CN 19 18778479 18778479 single base substitution T C missense_variant M119T 356T>C COCA-CN 19 18778479 18778479 single base substitution T C missense_variant M91T 272T>C COCA-CN 19 18778901 18778901 single base substitution C T downstream_gene_variant COCA-CN 19 18778901 18778901 single base substitution C T intron_variant COCA-CN 19 18778901 18778901 single base substitution C T missense_variant R232C 694C>T COCA-CN 19 18779152 18779152 single base substitution C T downstream_gene_variant COCA-CN 19 18779152 18779152 single base substitution C T intron_variant COCA-CN 19 18779152 18779152 single base substitution C T synonymous_variant G315G 945C>T COCA-CN 19 18779200 18779200 single base substitution C T downstream_gene_variant COCA-CN 19 18779200 18779200 single base substitution C T intron_variant COCA-CN 19 18779200 18779200 single base substitution C T synonymous_variant Y331Y 993C>T COCA-CN 19 18779850 18779850 single base substitution G A downstream_gene_variant COCA-CN 19 18779850 18779850 single base substitution G A intron_variant COCA-CN 19 18779850 18779850 single base substitution G A missense_variant G548D 1643G>A COCA-CN 19 18780070 18780070 single base substitution G A 3_prime_UTR_variant COCA-CN 19 18780070 18780070 single base substitution G A downstream_gene_variant COCA-CN 19 18780070 18780070 single base substitution G A missense_variant G142R 424G>A ESAD-UK 19 18744106 18744106 single base substitution G C upstream_gene_variant ESAD-UK 19 18747691 18747691 single base substitution C A upstream_gene_variant ESAD-UK 19 18748778 18748778 single base substitution T C intron_variant ESAD-UK 19 18749527 18749527 single base substitution C T intron_variant ESAD-UK 19 18749531 18749531 single base substitution C T intron_variant ESAD-UK 19 18749633 18749633 single base substitution C G intron_variant ESAD-UK 19 18750084 18750084 single base substitution C T intron_variant ESAD-UK 19 18750094 18750094 single base substitution C A intron_variant ESAD-UK 19 18750266 18750266 single base substitution C T intron_variant ESAD-UK 19 18750458 18750458 single base substitution G A intron_variant ESAD-UK 19 18750458 18750458 single base substitution G A upstream_gene_variant ESAD-UK 19 18750926 18750926 single base substitution G C intron_variant ESAD-UK 19 18750926 18750926 single base substitution G C upstream_gene_variant ESAD-UK 19 18751120 18751120 single base substitution C T intron_variant ESAD-UK 19 18751120 18751120 single base substitution C T upstream_gene_variant ESAD-UK 19 18758270 18758270 insertion of <=200bp - TG intron_variant ESAD-UK 19 18758768 18758768 single base substitution G A intron_variant ESAD-UK 19 18762427 18762427 single base substitution C T intron_variant ESAD-UK 19 18763138 18763138 single base substitution G A intron_variant ESAD-UK 19 18765017 18765017 single base substitution C T intron_variant ESAD-UK 19 18768867 18768867 single base substitution C T intron_variant ESAD-UK 19 18773158 18773158 single base substitution C A intron_variant ESAD-UK 19 18773250 18773250 single base substitution G A intron_variant ESAD-UK 19 18774281 18774281 single base substitution G A intron_variant ESAD-UK 19 18775110 18775110 single base substitution G A 3_prime_UTR_variant ESAD-UK 19 18775110 18775110 single base substitution G A exon_variant ESAD-UK 19 18775110 18775110 single base substitution G A synonymous_variant S40S 120G>A ESAD-UK 19 18775110 18775110 single base substitution G A synonymous_variant S41S 123G>A ESAD-UK 19 18777907 18777907 single base substitution G T intron_variant ESAD-UK 19 18779455 18779455 single base substitution C T downstream_gene_variant ESAD-UK 19 18779455 18779455 single base substitution C T intron_variant ESAD-UK 19 18779455 18779455 single base substitution C T synonymous_variant Y416Y 1248C>T ESAD-UK 19 18780763 18780763 single base substitution C T 3_prime_UTR_variant ESAD-UK 19 18780763 18780763 single base substitution C T downstream_gene_variant ESAD-UK 19 18783649 18783649 insertion of <=200bp - GA downstream_gene_variant ESCA-CN 19 18775156 18775156 single base substitution C T 3_prime_UTR_variant ESCA-CN 19 18775156 18775156 single base substitution C T exon_variant ESCA-CN 19 18775156 18775156 single base substitution C T missense_variant R56C 166C>T ESCA-CN 19 18775156 18775156 single base substitution C T missense_variant R57C 169C>T ESCA-CN 19 18778787 18778787 single base substitution C A downstream_gene_variant ESCA-CN 19 18778787 18778787 single base substitution C A exon_variant ESCA-CN 19 18778787 18778787 single base substitution C A intron_variant ESCA-CN 19 18778787 18778787 single base substitution C A missense_variant Q194K 580C>A GBM-US 19 18779533 18779533 single base substitution C T downstream_gene_variant GBM-US 19 18779533 18779533 single base substitution C T intron_variant GBM-US 19 18779533 18779533 single base substitution C T synonymous_variant Y442Y 1326C>T KIRC-US 19 18778755 18778755 single base substitution C G downstream_gene_variant KIRC-US 19 18778755 18778755 single base substitution C G exon_variant KIRC-US 19 18778755 18778755 single base substitution C G intron_variant KIRC-US 19 18778755 18778755 single base substitution C G missense_variant S183W 548C>G KIRP-US 19 18778682 18778682 single base substitution G A downstream_gene_variant KIRP-US 19 18778682 18778682 single base substitution G A exon_variant KIRP-US 19 18778682 18778682 single base substitution G A intron_variant KIRP-US 19 18778682 18778682 single base substitution G A missense_variant A159T 475G>A LAML-KR 19 18752147 18752147 single base substitution A T intron_variant LAML-KR 19 18752147 18752147 single base substitution A T upstream_gene_variant LAML-KR 19 18764478 18764478 single base substitution A T intron_variant LGG-US 19 18779269 18779269 single base substitution G A downstream_gene_variant LGG-US 19 18779269 18779269 single base substitution G A intron_variant LGG-US 19 18779269 18779269 single base substitution G A synonymous_variant T354T 1062G>A LICA-CN 19 18779267 18779267 single base substitution A T downstream_gene_variant LICA-CN 19 18779267 18779267 single base substitution A T intron_variant LICA-CN 19 18779267 18779267 single base substitution A T missense_variant T354S 1060A>T LICA-CN 19 18779881 18779881 single base substitution G A downstream_gene_variant LICA-CN 19 18779881 18779881 single base substitution G A intron_variant LICA-CN 19 18779881 18779881 single base substitution G A synonymous_variant E558E 1674G>A LICA-CN 19 18779957 18779957 single base substitution G A downstream_gene_variant LICA-CN 19 18779957 18779957 single base substitution G A intron_variant LICA-CN 19 18779957 18779957 single base substitution G A missense_variant D584N 1750G>A LICA-FR 19 18776224 18776224 single base substitution C T intron_variant LICA-FR 19 18779665 18779665 single base substitution C G downstream_gene_variant LICA-FR 19 18779665 18779665 single base substitution C G intron_variant LICA-FR 19 18779665 18779665 single base substitution C G missense_variant D486E 1458C>G LIHC-US 19 18779891 18779891 single base substitution T G downstream_gene_variant LIHC-US 19 18779891 18779891 single base substitution T G intron_variant LIHC-US 19 18779891 18779891 single base substitution T G missense_variant Y562D 1684T>G LINC-JP 19 18745711 18745711 single base substitution C T upstream_gene_variant LINC-JP 19 18750797 18750797 single base substitution C T intron_variant LINC-JP 19 18750797 18750797 single base substitution C T upstream_gene_variant LINC-JP 19 18756015 18756015 single base substitution G T intron_variant LINC-JP 19 18758898 18758898 single base substitution G A intron_variant LINC-JP 19 18767480 18767480 single base substitution A C intron_variant LINC-JP 19 18778306 18778306 single base substitution G A 3_prime_UTR_variant LINC-JP 19 18778306 18778306 single base substitution G A intron_variant LINC-JP 19 18778897 18778897 single base substitution C T downstream_gene_variant LINC-JP 19 18778897 18778897 single base substitution C T intron_variant LINC-JP 19 18778897 18778897 single base substitution C T synonymous_variant A230A 690C>T LINC-JP 19 18779949 18779949 single base substitution A G downstream_gene_variant LINC-JP 19 18779949 18779949 single base substitution A G intron_variant LINC-JP 19 18779949 18779949 single base substitution A G missense_variant Y581C 1742A>G LIRI-JP 19 18744207 18744207 single base substitution C T upstream_gene_variant LIRI-JP 19 18751025 18751025 single base substitution A G intron_variant LIRI-JP 19 18751025 18751025 single base substitution A G upstream_gene_variant LIRI-JP 19 18751588 18751588 single base substitution A G intron_variant LIRI-JP 19 18751588 18751588 single base substitution A G upstream_gene_variant LIRI-JP 19 18754191 18754191 single base substitution G T intron_variant LIRI-JP 19 18754191 18754191 single base substitution G T upstream_gene_variant LIRI-JP 19 18756197 18756197 single base substitution G A intron_variant LIRI-JP 19 18758333 18758333 single base substitution C A intron_variant LIRI-JP 19 18759428 18759428 single base substitution G A intron_variant LIRI-JP 19 18760275 18760275 single base substitution C A intron_variant LIRI-JP 19 18762602 18762602 single base substitution G A intron_variant LIRI-JP 19 18762648 18762648 single base substitution T G intron_variant LIRI-JP 19 18762676 18762676 single base substitution C A intron_variant LIRI-JP 19 18766183 18766183 single base substitution G A intron_variant LIRI-JP 19 18772902 18772902 deletion of <=200bp A - intron_variant LIRI-JP 19 18773267 18773267 single base substitution G T intron_variant LIRI-JP 19 18775961 18775961 single base substitution G T intron_variant LIRI-JP 19 18781230 18781230 single base substitution A G 3_prime_UTR_variant LIRI-JP 19 18781230 18781230 single base substitution A G downstream_gene_variant LIRI-JP 19 18783175 18783175 single base substitution G A downstream_gene_variant LIRI-JP 19 18784708 18784708 single base substitution G A downstream_gene_variant LUSC-KR 19 18743485 18743485 single base substitution A C upstream_gene_variant LUSC-KR 19 18747425 18747425 single base substitution C T upstream_gene_variant LUSC-KR 19 18756256 18756256 single base substitution G C intron_variant LUSC-KR 19 18756770 18756770 single base substitution G T intron_variant LUSC-KR 19 18763590 18763590 single base substitution A G intron_variant LUSC-KR 19 18765696 18765696 single base substitution A T intron_variant LUSC-KR 19 18769313 18769313 single base substitution G C intron_variant LUSC-KR 19 18770887 18770887 single base substitution C A intron_variant LUSC-KR 19 18779030 18779030 single base substitution G A downstream_gene_variant LUSC-KR 19 18779030 18779030 single base substitution G A intron_variant LUSC-KR 19 18779030 18779030 single base substitution G A missense_variant V275M 823G>A LUSC-KR 19 18780002 18780002 single base substitution G T downstream_gene_variant LUSC-KR 19 18780002 18780002 single base substitution G T intron_variant LUSC-KR 19 18780002 18780002 single base substitution G T missense_variant A599S 1795G>T LUSC-KR 19 18780799 18780799 single base substitution C T 3_prime_UTR_variant LUSC-KR 19 18780799 18780799 single base substitution C T downstream_gene_variant LUSC-KR 19 18782832 18782832 single base substitution A T downstream_gene_variant LUSC-US 19 18778613 18778613 single base substitution G T 3_prime_UTR_variant LUSC-US 19 18778613 18778613 single base substitution G T downstream_gene_variant LUSC-US 19 18778613 18778613 single base substitution G T exon_variant LUSC-US 19 18778613 18778613 single base substitution G T missense_variant V136L 406G>T LUSC-US 19 18778613 18778613 single base substitution G T missense_variant V164L 490G>T LUSC-US 19 18778613 18778613 single base substitution G T splice_donor_variant LUSC-US 19 18778681 18778681 single base substitution G A downstream_gene_variant LUSC-US 19 18778681 18778681 single base substitution G A exon_variant LUSC-US 19 18778681 18778681 single base substitution G A intron_variant LUSC-US 19 18778681 18778681 single base substitution G A synonymous_variant A158A 474G>A LUSC-US 19 18778777 18778777 single base substitution G C downstream_gene_variant LUSC-US 19 18778777 18778777 single base substitution G C exon_variant LUSC-US 19 18778777 18778777 single base substitution G C intron_variant LUSC-US 19 18778777 18778777 single base substitution G C synonymous_variant R190R 570G>C LUSC-US 19 18779381 18779381 single base substitution C T downstream_gene_variant LUSC-US 19 18779381 18779381 single base substitution C T intron_variant LUSC-US 19 18779381 18779381 single base substitution C T missense_variant R392C 1174C>T LUSC-US 19 18779702 18779702 single base substitution G A downstream_gene_variant LUSC-US 19 18779702 18779702 single base substitution G A intron_variant LUSC-US 19 18779702 18779702 single base substitution G A missense_variant V499M 1495G>A MALY-DE 19 18743574 18743574 single base substitution T C upstream_gene_variant MALY-DE 19 18743856 18743856 single base substitution T C upstream_gene_variant MALY-DE 19 18752061 18752061 single base substitution T C intron_variant MALY-DE 19 18752061 18752061 single base substitution T C upstream_gene_variant MALY-DE 19 18756098 18756098 single base substitution C T intron_variant MALY-DE 19 18757552 18757552 single base substitution G A intron_variant MALY-DE 19 18779369 18779369 single base substitution C A downstream_gene_variant MALY-DE 19 18779369 18779369 single base substitution C A intron_variant MALY-DE 19 18779369 18779369 single base substitution C A missense_variant P388T 1162C>A MALY-DE 19 18779953 18779953 single base substitution C A downstream_gene_variant MALY-DE 19 18779953 18779953 single base substitution C A intron_variant MALY-DE 19 18779953 18779953 single base substitution C A missense_variant N582K 1746C>A MALY-DE 19 18784817 18784817 single base substitution G A downstream_gene_variant MALY-DE 19 18786125 18786125 single base substitution A G downstream_gene_variant MELA-AU 19 18742819 18742819 single base substitution G A upstream_gene_variant MELA-AU 19 18742878 18742878 single base substitution C T upstream_gene_variant MELA-AU 19 18743120 18743120 single base substitution G T upstream_gene_variant MELA-AU 19 18743122 18743122 single base substitution C A upstream_gene_variant MELA-AU 19 18743211 18743211 single base substitution A T upstream_gene_variant MELA-AU 19 18743451 18743451 single base substitution G A upstream_gene_variant MELA-AU 19 18744236 18744236 single base substitution G A upstream_gene_variant MELA-AU 19 18744347 18744347 single base substitution T C upstream_gene_variant MELA-AU 19 18744647 18744647 single base substitution G A upstream_gene_variant MELA-AU 19 18744669 18744669 single base substitution C T upstream_gene_variant MELA-AU 19 18744955 18744955 single base substitution C T upstream_gene_variant MELA-AU 19 18744976 18744976 single base substitution G A upstream_gene_variant MELA-AU 19 18745345 18745345 single base substitution G A upstream_gene_variant MELA-AU 19 18745533 18745533 single base substitution C T upstream_gene_variant MELA-AU 19 18745535 18745535 single base substitution C T upstream_gene_variant MELA-AU 19 18745939 18745939 insertion of <=200bp - GT upstream_gene_variant MELA-AU 19 18745990 18745990 single base substitution C A upstream_gene_variant MELA-AU 19 18746517 18746517 single base substitution G A upstream_gene_variant MELA-AU 19 18747196 18747196 single base substitution C T upstream_gene_variant MELA-AU 19 18747218 18747218 single base substitution C T upstream_gene_variant MELA-AU 19 18747436 18747436 single base substitution C T upstream_gene_variant MELA-AU 19 18747636 18747636 single base substitution G A upstream_gene_variant MELA-AU 19 18748604 18748604 single base substitution C T intron_variant MELA-AU 19 18748612 18748612 single base substitution C T intron_variant MELA-AU 19 18749912 18749912 single base substitution A G intron_variant MELA-AU 19 18750144 18750144 single base substitution C T intron_variant MELA-AU 19 18750310 18750310 single base substitution C T intron_variant MELA-AU 19 18751135 18751136 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 18751135 18751136 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 18751447 18751447 single base substitution C T intron_variant MELA-AU 19 18751447 18751447 single base substitution C T upstream_gene_variant MELA-AU 19 18751590 18751590 single base substitution C T intron_variant MELA-AU 19 18751590 18751590 single base substitution C T upstream_gene_variant MELA-AU 19 18751600 18751600 single base substitution C T intron_variant MELA-AU 19 18751600 18751600 single base substitution C T upstream_gene_variant MELA-AU 19 18751683 18751683 single base substitution C T intron_variant MELA-AU 19 18751683 18751683 single base substitution C T upstream_gene_variant MELA-AU 19 18752177 18752177 single base substitution G A intron_variant MELA-AU 19 18752177 18752177 single base substitution G A upstream_gene_variant MELA-AU 19 18752776 18752776 single base substitution C T intron_variant MELA-AU 19 18752776 18752776 single base substitution C T upstream_gene_variant MELA-AU 19 18753399 18753399 single base substitution C T intron_variant MELA-AU 19 18753399 18753399 single base substitution C T upstream_gene_variant MELA-AU 19 18753674 18753674 single base substitution C T intron_variant MELA-AU 19 18753674 18753674 single base substitution C T upstream_gene_variant MELA-AU 19 18754178 18754178 single base substitution C T intron_variant MELA-AU 19 18754178 18754178 single base substitution C T upstream_gene_variant MELA-AU 19 18754209 18754209 single base substitution C T intron_variant MELA-AU 19 18754209 18754209 single base substitution C T upstream_gene_variant MELA-AU 19 18754291 18754291 single base substitution T A intron_variant MELA-AU 19 18754291 18754291 single base substitution T A upstream_gene_variant MELA-AU 19 18754512 18754513 multiple base substitution (>=2bp and <=200bp) TC GT intron_variant MELA-AU 19 18754512 18754513 multiple base substitution (>=2bp and <=200bp) TC GT upstream_gene_variant MELA-AU 19 18754630 18754630 single base substitution C T intron_variant MELA-AU 19 18754630 18754630 single base substitution C T upstream_gene_variant MELA-AU 19 18754686 18754686 single base substitution G A intron_variant MELA-AU 19 18754686 18754686 single base substitution G A upstream_gene_variant MELA-AU 19 18754794 18754794 single base substitution C T intron_variant MELA-AU 19 18754794 18754794 single base substitution C T upstream_gene_variant MELA-AU 19 18755325 18755325 single base substitution T C intron_variant MELA-AU 19 18755325 18755325 single base substitution T C upstream_gene_variant MELA-AU 19 18755520 18755520 single base substitution C T intron_variant MELA-AU 19 18755722 18755722 single base substitution C T intron_variant MELA-AU 19 18755843 18755843 single base substitution G A intron_variant MELA-AU 19 18756559 18756559 single base substitution T C intron_variant MELA-AU 19 18756873 18756873 single base substitution C T intron_variant MELA-AU 19 18757151 18757151 single base substitution C T intron_variant MELA-AU 19 18757244 18757244 single base substitution C T intron_variant MELA-AU 19 18757339 18757339 single base substitution C T intron_variant MELA-AU 19 18757417 18757417 single base substitution C T intron_variant MELA-AU 19 18757728 18757728 single base substitution C T intron_variant MELA-AU 19 18757964 18757964 single base substitution G A intron_variant MELA-AU 19 18758295 18758295 single base substitution T A intron_variant MELA-AU 19 18758811 18758811 single base substitution C T intron_variant MELA-AU 19 18759063 18759063 single base substitution C T intron_variant MELA-AU 19 18759562 18759562 single base substitution C T intron_variant MELA-AU 19 18759759 18759759 single base substitution C T intron_variant MELA-AU 19 18760620 18760620 single base substitution C T intron_variant MELA-AU 19 18760973 18760973 single base substitution C T intron_variant MELA-AU 19 18762250 18762250 single base substitution C T intron_variant MELA-AU 19 18763053 18763053 single base substitution C T intron_variant MELA-AU 19 18763147 18763147 single base substitution C T intron_variant MELA-AU 19 18763393 18763394 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 18763539 18763539 single base substitution C T intron_variant MELA-AU 19 18763583 18763583 single base substitution C T intron_variant MELA-AU 19 18763715 18763715 single base substitution T A intron_variant MELA-AU 19 18763782 18763782 single base substitution G A intron_variant MELA-AU 19 18763932 18763932 single base substitution C T intron_variant MELA-AU 19 18765527 18765527 single base substitution C T intron_variant MELA-AU 19 18765674 18765674 single base substitution C T intron_variant MELA-AU 19 18765884 18765884 single base substitution C T intron_variant MELA-AU 19 18765990 18765990 single base substitution C T intron_variant MELA-AU 19 18766124 18766124 single base substitution G A intron_variant MELA-AU 19 18766330 18766330 single base substitution C T intron_variant MELA-AU 19 18766334 18766334 single base substitution C T intron_variant MELA-AU 19 18766518 18766518 single base substitution T C intron_variant MELA-AU 19 18767089 18767089 single base substitution C T intron_variant MELA-AU 19 18767108 18767108 single base substitution C T intron_variant MELA-AU 19 18767123 18767123 single base substitution C T intron_variant MELA-AU 19 18767135 18767135 single base substitution C T intron_variant MELA-AU 19 18767379 18767379 single base substitution C T intron_variant MELA-AU 19 18767867 18767867 single base substitution C T intron_variant MELA-AU 19 18767881 18767881 single base substitution C T intron_variant MELA-AU 19 18767953 18767953 single base substitution C T intron_variant MELA-AU 19 18768003 18768003 single base substitution C T intron_variant MELA-AU 19 18768234 18768234 single base substitution C T intron_variant MELA-AU 19 18768389 18768389 single base substitution C T intron_variant MELA-AU 19 18768414 18768414 single base substitution C T intron_variant MELA-AU 19 18768995 18768995 single base substitution C T intron_variant MELA-AU 19 18769416 18769416 single base substitution C T intron_variant MELA-AU 19 18769791 18769791 single base substitution C T intron_variant MELA-AU 19 18769911 18769911 single base substitution C T intron_variant MELA-AU 19 18769973 18769973 single base substitution C T intron_variant MELA-AU 19 18770131 18770131 single base substitution C T intron_variant MELA-AU 19 18770366 18770366 single base substitution C T intron_variant MELA-AU 19 18770407 18770407 single base substitution G A intron_variant MELA-AU 19 18770440 18770440 single base substitution G A intron_variant MELA-AU 19 18771026 18771026 single base substitution G A intron_variant MELA-AU 19 18771309 18771309 single base substitution C T intron_variant MELA-AU 19 18772813 18772813 single base substitution C T intron_variant MELA-AU 19 18773033 18773033 single base substitution C T intron_variant MELA-AU 19 18773395 18773395 single base substitution G C intron_variant MELA-AU 19 18773763 18773763 single base substitution C T intron_variant MELA-AU 19 18774373 18774373 single base substitution C T intron_variant MELA-AU 19 18774467 18774467 single base substitution C T intron_variant MELA-AU 19 18774859 18774859 single base substitution C T intron_variant MELA-AU 19 18774912 18774912 single base substitution C T intron_variant MELA-AU 19 18775173 18775173 single base substitution C T 3_prime_UTR_variant MELA-AU 19 18775173 18775173 single base substitution C T exon_variant MELA-AU 19 18775173 18775173 single base substitution C T synonymous_variant L61L 183C>T MELA-AU 19 18775173 18775173 single base substitution C T synonymous_variant L62L 186C>T MELA-AU 19 18775422 18775422 single base substitution C T intron_variant MELA-AU 19 18775687 18775688 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 18775742 18775742 single base substitution C T intron_variant MELA-AU 19 18775989 18775989 single base substitution C T intron_variant MELA-AU 19 18776314 18776315 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 18776464 18776464 single base substitution C T intron_variant MELA-AU 19 18776754 18776754 single base substitution C T intron_variant MELA-AU 19 18777338 18777338 single base substitution C T intron_variant MELA-AU 19 18777638 18777638 single base substitution G T intron_variant MELA-AU 19 18777688 18777688 single base substitution C T intron_variant MELA-AU 19 18777697 18777697 single base substitution C T intron_variant MELA-AU 19 18778561 18778561 single base substitution C T 3_prime_UTR_variant MELA-AU 19 18778561 18778561 single base substitution C T downstream_gene_variant MELA-AU 19 18778561 18778561 single base substitution C T exon_variant MELA-AU 19 18778561 18778561 single base substitution C T synonymous_variant I118I 354C>T MELA-AU 19 18778561 18778561 single base substitution C T synonymous_variant I146I 438C>T MELA-AU 19 18778967 18778967 single base substitution C T downstream_gene_variant MELA-AU 19 18778967 18778967 single base substitution C T intron_variant MELA-AU 19 18778967 18778967 single base substitution C T missense_variant P254S 760C>T MELA-AU 19 18779095 18779095 single base substitution G A downstream_gene_variant MELA-AU 19 18779095 18779095 single base substitution G A intron_variant MELA-AU 19 18779095 18779095 single base substitution G A synonymous_variant E296E 888G>A MELA-AU 19 18779770 18779770 single base substitution C T downstream_gene_variant MELA-AU 19 18779770 18779770 single base substitution C T intron_variant MELA-AU 19 18779770 18779770 single base substitution C T synonymous_variant D521D 1563C>T MELA-AU 19 18779823 18779823 single base substitution G A downstream_gene_variant MELA-AU 19 18779823 18779823 single base substitution G A intron_variant MELA-AU 19 18779823 18779823 single base substitution G A stop_gained W539* 1616G>A MELA-AU 19 18780198 18780198 single base substitution C T 3_prime_UTR_variant MELA-AU 19 18780198 18780198 single base substitution C T downstream_gene_variant MELA-AU 19 18780302 18780303 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 19 18780302 18780303 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 18780316 18780316 single base substitution C T 3_prime_UTR_variant MELA-AU 19 18780316 18780316 single base substitution C T downstream_gene_variant MELA-AU 19 18780647 18780647 single base substitution C T 3_prime_UTR_variant MELA-AU 19 18780647 18780647 single base substitution C T downstream_gene_variant MELA-AU 19 18780955 18780955 single base substitution C T 3_prime_UTR_variant MELA-AU 19 18780955 18780955 single base substitution C T downstream_gene_variant MELA-AU 19 18780967 18780967 single base substitution C T 3_prime_UTR_variant MELA-AU 19 18780967 18780967 single base substitution C T downstream_gene_variant MELA-AU 19 18780967 18780968 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 19 18780967 18780968 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 18781275 18781275 single base substitution C T 3_prime_UTR_variant MELA-AU 19 18781275 18781275 single base substitution C T downstream_gene_variant MELA-AU 19 18781429 18781430 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 18781811 18781811 single base substitution C T downstream_gene_variant MELA-AU 19 18781978 18781978 single base substitution G A downstream_gene_variant MELA-AU 19 18782143 18782143 single base substitution C T downstream_gene_variant MELA-AU 19 18782166 18782166 single base substitution G A downstream_gene_variant MELA-AU 19 18782483 18782483 single base substitution C T downstream_gene_variant MELA-AU 19 18782825 18782825 single base substitution G A downstream_gene_variant MELA-AU 19 18782984 18782984 single base substitution C T downstream_gene_variant MELA-AU 19 18783036 18783036 single base substitution C T downstream_gene_variant MELA-AU 19 18783047 18783047 single base substitution C T downstream_gene_variant MELA-AU 19 18783072 18783072 single base substitution C T downstream_gene_variant MELA-AU 19 18783112 18783112 single base substitution C G downstream_gene_variant MELA-AU 19 18783492 18783492 single base substitution C T downstream_gene_variant MELA-AU 19 18783565 18783565 single base substitution C T downstream_gene_variant MELA-AU 19 18784739 18784739 single base substitution G A downstream_gene_variant MELA-AU 19 18785592 18785592 single base substitution C T downstream_gene_variant MELA-AU 19 18785660 18785660 single base substitution C T downstream_gene_variant MELA-AU 19 18785758 18785758 single base substitution A T downstream_gene_variant MELA-AU 19 18785873 18785873 single base substitution C T downstream_gene_variant MELA-AU 19 18785882 18785882 single base substitution C A downstream_gene_variant MELA-AU 19 18786190 18786190 single base substitution C T downstream_gene_variant ORCA-IN 19 18753193 18753193 single base substitution T G intron_variant ORCA-IN 19 18753193 18753193 single base substitution T G upstream_gene_variant ORCA-IN 19 18764037 18764037 single base substitution C T intron_variant ORCA-IN 19 18774280 18774280 single base substitution C T intron_variant ORCA-IN 19 18779845 18779845 single base substitution G A downstream_gene_variant ORCA-IN 19 18779845 18779845 single base substitution G A intron_variant ORCA-IN 19 18779845 18779845 single base substitution G A synonymous_variant R546R 1638G>A OV-AU 19 18743097 18743097 single base substitution G T upstream_gene_variant OV-AU 19 18747900 18747900 single base substitution T G exon_variant OV-AU 19 18747900 18747900 single base substitution T G synonymous_variant G11G 33T>G OV-AU 19 18747900 18747900 single base substitution T G synonymous_variant G12G 36T>G OV-AU 19 18749084 18749084 single base substitution T C intron_variant OV-AU 19 18754443 18754443 single base substitution C A intron_variant OV-AU 19 18754443 18754443 single base substitution C A upstream_gene_variant OV-AU 19 18762572 18762572 single base substitution T G intron_variant OV-AU 19 18763061 18763061 single base substitution A G intron_variant OV-AU 19 18763752 18763752 single base substitution G A intron_variant OV-AU 19 18766314 18766314 single base substitution C G intron_variant OV-AU 19 18767235 18767235 single base substitution C T intron_variant OV-AU 19 18770376 18770376 single base substitution C T intron_variant OV-AU 19 18772078 18772078 single base substitution C A intron_variant OV-AU 19 18773647 18773647 single base substitution G A intron_variant OV-AU 19 18775159 18775159 single base substitution G A 3_prime_UTR_variant OV-AU 19 18775159 18775159 single base substitution G A exon_variant OV-AU 19 18775159 18775159 single base substitution G A missense_variant A57T 169G>A OV-AU 19 18775159 18775159 single base substitution G A missense_variant A58T 172G>A OV-AU 19 18777661 18777661 single base substitution G C intron_variant OV-AU 19 18778050 18778050 single base substitution C A intron_variant OV-AU 19 18780758 18780758 single base substitution G C 3_prime_UTR_variant OV-AU 19 18780758 18780758 single base substitution G C downstream_gene_variant OV-AU 19 18785182 18785182 single base substitution T C downstream_gene_variant OV-US 19 18779040 18779040 single base substitution G A downstream_gene_variant OV-US 19 18779040 18779040 single base substitution G A intron_variant OV-US 19 18779040 18779040 single base substitution G A missense_variant R278H 833G>A PACA-AU 19 18743589 18743589 single base substitution G C upstream_gene_variant PACA-AU 19 18745939 18745939 insertion of <=200bp - GT upstream_gene_variant PACA-AU 19 18748889 18748889 single base substitution A C intron_variant PACA-AU 19 18750138 18750138 single base substitution G A intron_variant PACA-AU 19 18753465 18753465 single base substitution C T intron_variant PACA-AU 19 18753465 18753465 single base substitution C T upstream_gene_variant PACA-AU 19 18754245 18754245 single base substitution A G intron_variant PACA-AU 19 18754245 18754245 single base substitution A G upstream_gene_variant PACA-AU 19 18754711 18754711 single base substitution T C intron_variant PACA-AU 19 18754711 18754711 single base substitution T C upstream_gene_variant PACA-AU 19 18758270 18758270 insertion of <=200bp - TG intron_variant PACA-AU 19 18772078 18772078 single base substitution C T intron_variant PACA-AU 19 18778604 18778604 single base substitution G A 3_prime_UTR_variant PACA-AU 19 18778604 18778604 single base substitution G A downstream_gene_variant PACA-AU 19 18778604 18778604 single base substitution G A exon_variant PACA-AU 19 18778604 18778604 single base substitution G A missense_variant V133M 397G>A PACA-AU 19 18778604 18778604 single base substitution G A missense_variant V161M 481G>A PACA-AU 19 18778793 18778793 single base substitution G A downstream_gene_variant PACA-AU 19 18778793 18778793 single base substitution G A exon_variant PACA-AU 19 18778793 18778793 single base substitution G A intron_variant PACA-AU 19 18778793 18778793 single base substitution G A missense_variant A196T 586G>A PACA-AU 19 18778799 18778800 multiple base substitution (>=2bp and <=200bp) GA TT downstream_gene_variant PACA-AU 19 18778799 18778800 multiple base substitution (>=2bp and <=200bp) GA TT exon_variant PACA-AU 19 18778799 18778800 multiple base substitution (>=2bp and <=200bp) GA TT intron_variant PACA-AU 19 18778799 18778800 multiple base substitution (>=2bp and <=200bp) GA TT missense_variant E198L 592GA>TT PACA-AU 19 18779916 18779916 single base substitution G A downstream_gene_variant PACA-AU 19 18779916 18779916 single base substitution G A intron_variant PACA-AU 19 18779916 18779916 single base substitution G A missense_variant R570H 1709G>A PACA-AU 19 18781625 18781625 single base substitution A C downstream_gene_variant PACA-AU 19 18782211 18782211 single base substitution C G downstream_gene_variant PACA-CA 19 18745509 18745509 single base substitution C T upstream_gene_variant PACA-CA 19 18745806 18745806 single base substitution A G upstream_gene_variant PACA-CA 19 18748597 18748597 single base substitution G A intron_variant PACA-CA 19 18748688 18748688 single base substitution G A intron_variant PACA-CA 19 18750675 18750675 single base substitution T G intron_variant PACA-CA 19 18750675 18750675 single base substitution T G upstream_gene_variant PACA-CA 19 18754299 18754299 single base substitution T A intron_variant PACA-CA 19 18754299 18754299 single base substitution T A upstream_gene_variant PACA-CA 19 18754424 18754424 single base substitution G C intron_variant PACA-CA 19 18754424 18754424 single base substitution G C upstream_gene_variant PACA-CA 19 18754954 18754954 single base substitution G A intron_variant PACA-CA 19 18754954 18754954 single base substitution G A upstream_gene_variant PACA-CA 19 18754955 18754955 single base substitution G T intron_variant PACA-CA 19 18754955 18754955 single base substitution G T upstream_gene_variant PACA-CA 19 18760140 18760140 single base substitution C T intron_variant PACA-CA 19 18764062 18764062 single base substitution A G intron_variant PACA-CA 19 18773244 18773244 single base substitution G T intron_variant PACA-CA 19 18775378 18775378 single base substitution C T intron_variant PACA-CA 19 18777348 18777348 single base substitution C A intron_variant PACA-CA 19 18782632 18782632 single base substitution C T downstream_gene_variant PACA-CA 19 18782639 18782639 single base substitution C T downstream_gene_variant PAEN-AU 19 18743440 18743440 single base substitution G A upstream_gene_variant PAEN-AU 19 18756447 18756447 insertion of <=200bp - C intron_variant PAEN-AU 19 18769825 18769825 single base substitution G A intron_variant PAEN-AU 19 18777238 18777238 single base substitution G T intron_variant PAEN-IT 19 18745589 18745589 single base substitution T C upstream_gene_variant PBCA-DE 19 18745545 18745545 single base substitution C T upstream_gene_variant PBCA-DE 19 18745870 18745870 single base substitution T G upstream_gene_variant PBCA-DE 19 18747086 18747086 single base substitution A C upstream_gene_variant PBCA-DE 19 18753149 18753150 deletion of <=200bp GT - intron_variant PBCA-DE 19 18753149 18753150 deletion of <=200bp GT - upstream_gene_variant PBCA-DE 19 18756950 18756950 insertion of <=200bp - T intron_variant PBCA-DE 19 18767203 18767203 single base substitution C T intron_variant PBCA-DE 19 18767983 18767983 single base substitution C G intron_variant PBCA-DE 19 18779360 18779360 single base substitution C T downstream_gene_variant PBCA-DE 19 18779360 18779360 single base substitution C T intron_variant PBCA-DE 19 18779360 18779360 single base substitution C T missense_variant R385C 1153C>T PBCA-DE 19 18782351 18782351 single base substitution C T downstream_gene_variant PRAD-CA 19 18754125 18754125 single base substitution C T intron_variant PRAD-CA 19 18754125 18754125 single base substitution C T upstream_gene_variant PRAD-CA 19 18773306 18773306 single base substitution G A intron_variant PRAD-CA 19 18775424 18775424 single base substitution C T intron_variant PRAD-UK 19 18766522 18766522 insertion of <=200bp - GCTGGTCAGGGAGGTGGGGTCTGAACACCCCCTTGTCTTCATGCTATGGAGGCAGAGAGCTTGCC intron_variant PRAD-UK 19 18772821 18772821 single base substitution C G intron_variant PRAD-US 19 18778497 18778497 single base substitution G A 3_prime_UTR_variant PRAD-US 19 18778497 18778497 single base substitution G A downstream_gene_variant PRAD-US 19 18778497 18778497 single base substitution G A exon_variant PRAD-US 19 18778497 18778497 single base substitution G A missense_variant R125Q 374G>A PRAD-US 19 18778497 18778497 single base substitution G A missense_variant R97Q 290G>A READ-US 19 18779181 18779181 single base substitution C T downstream_gene_variant READ-US 19 18779181 18779181 single base substitution C T intron_variant READ-US 19 18779181 18779181 single base substitution C T missense_variant S325L 974C>T RECA-EU 19 18743635 18743635 single base substitution T C upstream_gene_variant RECA-EU 19 18746068 18746068 single base substitution C T upstream_gene_variant RECA-EU 19 18770759 18770759 single base substitution G A intron_variant SKCA-BR 19 18743260 18743260 single base substitution C T upstream_gene_variant SKCA-BR 19 18743573 18743573 single base substitution A G upstream_gene_variant SKCA-BR 19 18743969 18743969 single base substitution T A upstream_gene_variant SKCA-BR 19 18745056 18745056 single base substitution A G upstream_gene_variant SKCA-BR 19 18745205 18745205 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 19 18745534 18745534 single base substitution C T upstream_gene_variant SKCA-BR 19 18747862 18747862 single base substitution A G 5_prime_UTR_variant SKCA-BR 19 18747862 18747862 single base substitution A G upstream_gene_variant SKCA-BR 19 18753830 18753830 single base substitution G A intron_variant SKCA-BR 19 18753830 18753830 single base substitution G A upstream_gene_variant SKCA-BR 19 18757557 18757557 single base substitution C T intron_variant SKCA-BR 19 18761831 18761831 single base substitution C T intron_variant SKCA-BR 19 18763596 18763596 single base substitution T C intron_variant SKCA-BR 19 18766131 18766131 single base substitution C T intron_variant SKCA-BR 19 18766843 18766843 single base substitution C T intron_variant SKCA-BR 19 18769289 18769289 insertion of <=200bp - GTCTCTCTGGGTCTCTGTCTCCC intron_variant SKCA-BR 19 18770119 18770119 single base substitution C T intron_variant SKCA-BR 19 18770461 18770461 insertion of <=200bp - CT intron_variant SKCA-BR 19 18772812 18772812 single base substitution C T intron_variant SKCA-BR 19 18774871 18774871 single base substitution C T intron_variant SKCA-BR 19 18775077 18775077 single base substitution C T 3_prime_UTR_variant SKCA-BR 19 18775077 18775077 single base substitution C T exon_variant SKCA-BR 19 18775077 18775077 single base substitution C T synonymous_variant A29A 87C>T SKCA-BR 19 18775077 18775077 single base substitution C T synonymous_variant A30A 90C>T SKCA-BR 19 18775689 18775689 single base substitution G A intron_variant SKCA-BR 19 18782210 18782210 single base substitution C T downstream_gene_variant SKCA-BR 19 18782284 18782284 single base substitution C T downstream_gene_variant SKCA-BR 19 18782463 18782463 single base substitution A C downstream_gene_variant SKCA-BR 19 18783493 18783493 single base substitution C T downstream_gene_variant SKCM-US 19 18775173 18775173 single base substitution C T 3_prime_UTR_variant SKCM-US 19 18775173 18775173 single base substitution C T exon_variant SKCM-US 19 18775173 18775173 single base substitution C T synonymous_variant L61L 183C>T SKCM-US 19 18775173 18775173 single base substitution C T synonymous_variant L62L 186C>T SKCM-US 19 18775198 18775198 single base substitution A G 3_prime_UTR_variant SKCM-US 19 18775198 18775198 single base substitution A G exon_variant SKCM-US 19 18775198 18775198 single base substitution A G missense_variant R70G 208A>G SKCM-US 19 18775198 18775198 single base substitution A G missense_variant R71G 211A>G SKCM-US 19 18775224 18775224 single base substitution C T 3_prime_UTR_variant SKCM-US 19 18775224 18775224 single base substitution C T exon_variant SKCM-US 19 18775224 18775224 single base substitution C T synonymous_variant V78V 234C>T SKCM-US 19 18775224 18775224 single base substitution C T synonymous_variant V79V 237C>T SKCM-US 19 18778511 18778511 single base substitution G A 3_prime_UTR_variant SKCM-US 19 18778511 18778511 single base substitution G A downstream_gene_variant SKCM-US 19 18778511 18778511 single base substitution G A exon_variant SKCM-US 19 18778511 18778511 single base substitution G A missense_variant D102N 304G>A SKCM-US 19 18778511 18778511 single base substitution G A missense_variant D130N 388G>A SKCM-US 19 18778631 18778631 single base substitution T G 3_prime_UTR_variant SKCM-US 19 18778631 18778631 single base substitution T G downstream_gene_variant SKCM-US 19 18778631 18778631 single base substitution T G exon_variant SKCM-US 19 18778631 18778631 single base substitution T G intron_variant SKCM-US 19 18778631 18778631 single base substitution T G missense_variant F142V 424T>G SKCM-US 19 18778631 18778631 single base substitution T G missense_variant F170V 508T>G SKCM-US 19 18778810 18778810 single base substitution C T downstream_gene_variant SKCM-US 19 18778810 18778810 single base substitution C T intron_variant SKCM-US 19 18778810 18778810 single base substitution C T synonymous_variant F201F 603C>T SKCM-US 19 18779140 18779140 single base substitution C T downstream_gene_variant SKCM-US 19 18779140 18779140 single base substitution C T intron_variant SKCM-US 19 18779140 18779140 single base substitution C T synonymous_variant L311L 933C>T SKCM-US 19 18779689 18779689 single base substitution G A downstream_gene_variant SKCM-US 19 18779689 18779689 single base substitution G A intron_variant SKCM-US 19 18779689 18779689 single base substitution G A missense_variant M494I 1482G>A SKCM-US 19 18779856 18779856 single base substitution C T downstream_gene_variant SKCM-US 19 18779856 18779856 single base substitution C T intron_variant SKCM-US 19 18779856 18779856 single base substitution C T missense_variant S550L 1649C>T STAD-US 19 18778576 18778576 single base substitution C T 3_prime_UTR_variant STAD-US 19 18778576 18778576 single base substitution C T downstream_gene_variant STAD-US 19 18778576 18778576 single base substitution C T exon_variant STAD-US 19 18778576 18778576 single base substitution C T synonymous_variant S123S 369C>T STAD-US 19 18778576 18778576 single base substitution C T synonymous_variant S151S 453C>T STAD-US 19 18778628 18778628 single base substitution G A 3_prime_UTR_variant STAD-US 19 18778628 18778628 single base substitution G A downstream_gene_variant STAD-US 19 18778628 18778628 single base substitution G A exon_variant STAD-US 19 18778628 18778628 single base substitution G A intron_variant STAD-US 19 18778628 18778628 single base substitution G A missense_variant V141M 421G>A STAD-US 19 18778628 18778628 single base substitution G A missense_variant V169M 505G>A STAD-US 19 18778859 18778859 single base substitution C T downstream_gene_variant STAD-US 19 18778859 18778859 single base substitution C T intron_variant STAD-US 19 18778859 18778859 single base substitution C T synonymous_variant L218L 652C>T STAD-US 19 18778890 18778890 single base substitution G A downstream_gene_variant STAD-US 19 18778890 18778890 single base substitution G A intron_variant STAD-US 19 18778890 18778890 single base substitution G A missense_variant R228H 683G>A STAD-US 19 18779089 18779089 single base substitution G A downstream_gene_variant STAD-US 19 18779089 18779089 single base substitution G A intron_variant STAD-US 19 18779089 18779089 single base substitution G A synonymous_variant Q294Q 882G>A STAD-US 19 18779108 18779108 single base substitution C T downstream_gene_variant STAD-US 19 18779108 18779108 single base substitution C T intron_variant STAD-US 19 18779108 18779108 single base substitution C T missense_variant R301C 901C>T STAD-US 19 18779306 18779306 deletion of <=200bp G - downstream_gene_variant STAD-US 19 18779306 18779306 deletion of <=200bp G - frameshift_variant G367 STAD-US 19 18779306 18779306 deletion of <=200bp G - intron_variant STAD-US 19 18779360 18779360 single base substitution C T downstream_gene_variant STAD-US 19 18779360 18779360 single base substitution C T intron_variant STAD-US 19 18779360 18779360 single base substitution C T missense_variant R385C 1153C>T STAD-US 19 18779651 18779651 single base substitution G A downstream_gene_variant STAD-US 19 18779651 18779651 single base substitution G A intron_variant STAD-US 19 18779651 18779651 single base substitution G A missense_variant D482N 1444G>A STAD-US 19 18779936 18779936 single base substitution A G downstream_gene_variant STAD-US 19 18779936 18779936 single base substitution A G intron_variant STAD-US 19 18779936 18779936 single base substitution A G missense_variant I577V 1729A>G STAD-US 19 18779982 18779982 single base substitution T C downstream_gene_variant STAD-US 19 18779982 18779982 single base substitution T C intron_variant STAD-US 19 18779982 18779982 single base substitution T C missense_variant L592P 1775T>C STAD-US 19 18780032 18780032 deletion of <=200bp C - downstream_gene_variant STAD-US 19 18780032 18780032 deletion of <=200bp C - frameshift_variant P609 STAD-US 19 18780032 18780032 deletion of <=200bp C - intron_variant THCA-SA 19 18775077 18775077 single base substitution C T 3_prime_UTR_variant THCA-SA 19 18775077 18775077 single base substitution C T exon_variant THCA-SA 19 18775077 18775077 single base substitution C T synonymous_variant A29A 87C>T THCA-SA 19 18775077 18775077 single base substitution C T synonymous_variant A30A 90C>T THCA-SA 19 18780769 18780769 single base substitution T C 3_prime_UTR_variant THCA-SA 19 18780769 18780769 single base substitution T C downstream_gene_variant THCA-US 19 18779952 18779952 single base substitution A T downstream_gene_variant THCA-US 19 18779952 18779952 single base substitution A T intron_variant THCA-US 19 18779952 18779952 single base substitution A T missense_variant N582I 1745A>T UCEC-US 19 18778567 18778567 single base substitution C T 3_prime_UTR_variant UCEC-US 19 18778567 18778567 single base substitution C T downstream_gene_variant UCEC-US 19 18778567 18778567 single base substitution C T exon_variant UCEC-US 19 18778567 18778567 single base substitution C T synonymous_variant F120F 360C>T UCEC-US 19 18778567 18778567 single base substitution C T synonymous_variant F148F 444C>T UCEC-US 19 18779747 18779747 single base substitution G A downstream_gene_variant UCEC-US 19 18779747 18779747 single base substitution G A intron_variant UCEC-US 19 18779747 18779747 single base substitution G A missense_variant G514R 1540G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LUAD-RT-S01818 COSM75167 c.833G>A p.R278H Substitution - Missense 19:18668230-18668230 + TCGA-HJ-7597-01 COSM4075721 c.1775T>C p.L592P Substitution - Missense 19:18669172-18669172 + B60-Tumor COSM1750733 c.426C>T p.F142F Substitution - coding silent 19:18667823-18667823 + C086 COSM5533468 c.1791C>T p.S597S Substitution - coding silent 19:18669188-18669188 + TCGA-MK-A4N6-01 COSM3371220 c.1745A>T p.N582I Substitution - Missense 19:18669142-18669142 + TCGA-EE-A29E-06 COSM3530845 c.933C>T p.L311L Substitution - coding silent 19:18668330-18668330 + CSCC-27-T COSM4563166 c.961G>A p.D321N Substitution - Missense 19:18668358-18668358 + OSCC-GB_01280111 COSM5954174 c.1638G>A p.R546R Substitution - coding silent 19:18669035-18669035 + ORL-48 COSM4596992 c.730G>C p.A244P Substitution - Missense 19:18668127-18668127 + TCGA-13-1509-01 COSM75167 c.833G>A p.R278H Substitution - Missense 19:18668230-18668230 + ESCC_BICR_050T COSM5440058 c.580C>A p.Q194K Substitution - Missense 19:18667977-18667977 + C70 COSM4619478 c.1831G>A p.A611T Substitution - Missense 19:18669228-18669228 + H1672 COSM312372 c.1471A>C p.K491Q Substitution - Missense 19:18668868-18668868 + WSU-HN12 COSM3100291 c.755G>A p.R252H Substitution - Missense 19:18668152-18668152 + CSCC-16-T COSM993131 c.1540G>A p.G514R Substitution - Missense 19:18668937-18668937 + CSCC-49-T COSM4505116 c.684C>T p.R228R Substitution - coding silent 19:18668081-18668081 + CHC1744T COSM4792381 c.1458C>G p.D486E Substitution - Missense 19:18668855-18668855 + TCGA-66-2756-01 COSM711099 c.570G>C p.R190R Substitution - coding silent 19:18667967-18667967 + 8044436 COSM3388740 c.592G>T p.E198* Substitution - Nonsense 19:18667989-18667989 + CSCC-40-T COSM4472424 c.1782C>T p.F594F Substitution - coding silent 19:18669179-18669179 + T3021 COSM1391712 c.1099delG p.Q369fs*22 Deletion - Frameshift 19:18668496-18668496 + B60-Tumor COSM1750734 c.630C>G p.V210V Substitution - coding silent 19:18668027-18668027 + SC_9046 COSM5562637 c.1602G>A p.P534P Substitution - coding silent 19:18668999-18668999 + TCGA-06-0122-01 COSM3403966 c.1326C>T p.Y442Y Substitution - coding silent 19:18668723-18668723 + SW480 COSM4655773 c.1026C>T p.R342R Substitution - coding silent 19:18668423-18668423 + 169 COSM3729719 c.484G>A p.V162M Substitution - Missense 19:18667881-18667881 + TCGA-RP-A695-06 COSM4896665 c.1649C>T p.S550L Substitution - Missense 19:18669046-18669046 + LIM2099 COSM4641122 c.1362T>A p.A454A Substitution - coding silent 19:18668759-18668759 + HN_62686 COSM126766 c.862C>T p.Q288* Substitution - Nonsense 19:18668259-18668259 + TCGA-HU-A4G8-01 COSM3100286 c.652C>T p.L218L Substitution - coding silent 19:18668049-18668049 + CSCC-31-T COSM1611841 c.690C>T p.A230A Substitution - coding silent 19:18668087-18668087 + 2334191 COSM321279 c.323G>T p.G108V Substitution - Missense 19:18667720-18667720 + ESO-2536 COSM1255975 c.417G>A p.A139A Substitution - coding silent 19:18667814-18667814 + S02351 COSM5695063 c.1546C>T p.R516C Substitution - Missense 19:18668943-18668943 + tumor_4182393 COSM5948271 c.1746C>A p.N582K Substitution - Missense 19:18669143-18669143 + NB2181 COSM5703129 c.107T>G p.L36R Substitution - Missense 19:18664284-18664284 + CHEWS031 COSM1239277 c.1755C>T p.T585T Substitution - coding silent 19:18669152-18669152 + LUAD-E01278 COSM394175 c.1647G>T p.Q549H Substitution - Missense 19:18669044-18669044 + CHEWS031 COSM711100 c.474G>A p.A158A Substitution - coding silent 19:18667871-18667871 + PD4120a COSM162028 c.468G>A p.L156L Substitution - coding silent 19:18667865-18667865 + TCGA-BP-5195-01 COSM474373 c.548C>G p.S183W Substitution - Missense 19:18667945-18667945 + 2492723 COSM5722901 c.182A>T p.Q61L Substitution - Missense 19:18664359-18664359 + TCGA-66-2759-01 COSM711098 c.1174C>T p.R392C Substitution - Missense 19:18668571-18668571 + C086 COSM5533469 c.504C>T p.I168I Substitution - coding silent 19:18667901-18667901 + HCC066T COSM5821029 c.1060A>T p.T354S Substitution - Missense 19:18668457-18668457 + 53M COSM711098 c.1174C>T p.R392C Substitution - Missense 19:18668571-18668571 + ccRCC-56 COSM1659561 c.1104delG p.Q369fs*22 Deletion - Frameshift 19:18668501-18668501 + HCC107T COSM1611841 c.690C>T p.A230A Substitution - coding silent 19:18668087-18668087 + P02-1562 COSM245316 c.264C>G p.F88L Substitution - Missense 19:18664441-18664441 + T55 COSM4696504 c.1117T>C p.Y373H Substitution - Missense 19:18668514-18668514 + 61 COSM5741508 c.1677G>T p.R559S Substitution - Missense 19:18669074-18669074 + YUFIT COSM5389130 c.123G>A p.S41S Substitution - coding silent 19:18664300-18664300 + S02375 COSM5702385 c.1568_1569GC>TT p.C523F Substitution - Missense 19:18668965-18668966 + HCC060T COSM5818086 c.1750G>A p.D584N Substitution - Missense 19:18669147-18669147 + TCGA-AF-2693-01 COSM1564613 c.974C>T p.S325L Substitution - Missense 19:18668371-18668371 + CRC-14T COSM5452111 c.945C>T p.G315G Substitution - coding silent 19:18668342-18668342 + CSCC-7-T COSM4468817 c.1564C>T p.R522C Substitution - Missense 19:18668961-18668961 + LP6007546-DNA_A01 COSM5389130 c.123G>A p.S41S Substitution - coding silent 19:18664300-18664300 + TCGA-A4-7287-01 COSM3989816 c.475G>A p.A159T Substitution - Missense 19:18667872-18667872 + TCGA-CA-6717-01 COSM1391709 c.295G>T p.A99S Substitution - Missense 19:18667692-18667692 + T3062 COSM4696505 c.1547G>A p.R516H Substitution - Missense 19:18668944-18668944 + 169 COSM3729718 c.416C>T p.A139V Substitution - Missense 19:18667813-18667813 + T2941 COSM3100310 c.1576G>A p.V526M Substitution - Missense 19:18668973-18668973 + B80-8-Tumor COSM1750735 c.976G>T p.V326F Substitution - Missense 19:18668373-18668373 + HCC73 COSM1611842 c.1742A>G p.Y581C Substitution - Missense 19:18669139-18669139 + TCGA-FW-A3R5-06 COSM3891970 c.237C>T p.V79V Substitution - coding silent 19:18664414-18664414 + 2492721 COSM5722901 c.182A>T p.Q61L Substitution - Missense 19:18664359-18664359 + 990149 COSM1644718 c.1756G>A p.D586N Substitution - Missense 19:18669153-18669153 + S02292 COSM5687610 c.651G>T p.R217R Substitution - coding silent 19:18668048-18668048 + TCGA-34-5927-01 COSM711097 c.1495G>A p.V499M Substitution - Missense 19:18668892-18668892 + TCGA-EZ-7264-01 COSM3970839 c.1062G>A p.T354T Substitution - coding silent 19:18668459-18668459 + T2944 COSM4075714 c.421G>A p.V141M Substitution - Missense 19:18667818-18667818 + BD72T COSM5513495 c.1335G>A p.S445S Substitution - coding silent 19:18668732-18668732 + 2492709 COSM5718021 c.564C>T p.T188T Substitution - coding silent 19:18667961-18667961 + TCGA-EE-A29L-06 COSM3530840 c.186C>T p.L62L Substitution - coding silent 19:18664363-18664363 + SNU-175 COSM3100297 c.1295G>A p.R432Q Substitution - Missense 19:18668692-18668692 + TCGA-G4-6311-01 COSM438980 c.90C>T p.A30A Substitution - coding silent 19:18664267-18664267 + YUWIA COSM3100309 c.1572C>T p.F524F Substitution - coding silent 19:18668969-18668969 + 8015299 COSM3770956 c.397G>A p.V133M Substitution - Missense 19:18667794-18667794 + C008 COSM3530844 c.603C>T p.F201F Substitution - coding silent 19:18668000-18668000 + Au4 COSM5603915 c.1563C>T p.D521D Substitution - coding silent 19:18668960-18668960 + B60 COSM1750734 c.630C>G p.V210V Substitution - coding silent 19:18668027-18668027 + UD-SCC-2 COSM4596992 c.730G>C p.A244P Substitution - Missense 19:18668127-18668127 + sysucc-1370T COSM3100288 c.694C>T p.R232C Substitution - Missense 19:18668091-18668091 + 8044436 COSM3388741 c.593A>T p.E198V Substitution - Missense 19:18667990-18667990 + ESO-859 COSM1239277 c.1755C>T p.T585T Substitution - coding silent 19:18669152-18669152 + 2492708 COSM5718021 c.564C>T p.T188T Substitution - coding silent 19:18667961-18667961 + 587342 COSM1212629 c.1360G>A p.A454T Substitution - Missense 19:18668757-18668757 + CSCC-62-T COSM4513539 c.942C>T p.F314F Substitution - coding silent 19:18668339-18668339 + TCGA-HU-A4H8-01 COSM4075718 c.1153C>T p.R385C Substitution - Missense 19:18668550-18668550 + 8068600 COSM252571 c.1709G>A p.R570H Substitution - Missense 19:18669106-18669106 + TCGA-BR-8382-01 COSM4075714 c.421G>A p.V141M Substitution - Missense 19:18667818-18667818 + TCGA-GV-A40G-01 COSM3796821 c.1035G>A p.T345T Substitution - coding silent 19:18668432-18668432 + TCGA-G3-A5SL-01 COSM4929559 c.1684T>G p.Y562D Substitution - Missense 19:18669081-18669081 + ESCC_157 COSM5646324 c.1129G>A p.E377K Substitution - Missense 19:18668526-18668526 + TP_2010 COSM5555386 c.1102G>C p.G368R Substitution - Missense 19:18668499-18668499 + TCGA-66-2742-01 COSM711100 c.474G>A p.A158A Substitution - coding silent 19:18667871-18667871 + SC_9062 COSM5552768 c.373G>C p.E125Q Substitution - Missense 19:18667770-18667770 + 2164 COSM5015592 c.1748C>T p.T583M Substitution - Missense 19:18669145-18669145 + CHC1744T COSM4792381 c.1458C>G p.D486E Substitution - Missense 19:18668855-18668855 + STC246 COSM5056401 c.1518C>A p.A506A Substitution - coding silent 19:18668915-18668915 + EGC8 COSM5056400 c.1125C>T p.S375S Substitution - coding silent 19:18668522-18668522 + TCGA-AU-6004-01 COSM1391712 c.1099delG p.Q369fs*22 Deletion - Frameshift 19:18668496-18668496 + 8044436 COSM4387526 c.592_593GA>TT p.E198L Substitution - Missense 19:18667989-18667990 + LP6007512-DNA_A01 COSM5033227 c.1248C>T p.Y416Y Substitution - coding silent 19:18668645-18668645 + sysucc-1317T COSM5449207 c.993C>T p.Y331Y Substitution - coding silent 19:18668390-18668390 + AOCS-139-12-5 COSM4140415 c.36T>G p.G12G Substitution - coding silent 19:18637090-18637090 + LC_S51 COSM1189954 c.595G>T p.E199* Substitution - Nonsense 19:18667992-18667992 + LC_S32 COSM1189955 c.1687A>G p.I563V Substitution - Missense 19:18669084-18669084 + TCGA-39-5016-01 COSM711101 c.406G>T p.V136L Substitution - Missense 19:18667803-18667803 + 2492710 COSM5718021 c.564C>T p.T188T Substitution - coding silent 19:18667961-18667961 + TCGA-FS-A1ZP-06 COSM3530843 c.304G>A p.D102N Substitution - Missense 19:18667701-18667701 + TCGA-BH-A18G-01 COSM3100316 c.1770G>A p.R590R Substitution - coding silent 19:18669167-18669167 + T658 COSM4696506 c.1617G>T p.W539C Substitution - Missense 19:18669014-18669014 + TCGA-HU-A4GQ-01 COSM4075715 c.683G>A p.R228H Substitution - Missense 19:18668080-18668080 + ML_15_T_01 COSM438980 c.90C>T p.A30A Substitution - coding silent 19:18664267-18664267 + ESO-250 COSM1255974 c.1258G>T p.G420C Substitution - Missense 19:18668655-18668655 + ESCC_25 COSM5626741 c.640C>G p.Q214E Substitution - Missense 19:18668037-18668037 + AOCS-106-1-1 COSM4140416 c.172G>A p.A58T Substitution - Missense 19:18664349-18664349 + TCGA-G4-6320-01 COSM1391712 c.1099delG p.Q369fs*22 Deletion - Frameshift 19:18668496-18668496 + TCGA-EE-A3J5-06 COSM3530844 c.603C>T p.F201F Substitution - coding silent 19:18668000-18668000 + 44_T COSM3959733 c.1449C>T p.P483P Substitution - coding silent 19:18668846-18668846 + sysucc-274T COSM5476045 c.1643G>A p.G548D Substitution - Missense 19:18669040-18669040 + TCGA-D9-A6EC-06 COSM4402946 c.424T>G p.F142V Substitution - Missense 19:18667821-18667821 + TCGA-BR-A4QL-01 COSM4075717 c.901C>T p.R301C Substitution - Missense 19:18668298-18668298 + CSCC-35-T COSM4523595 c.1221G>A p.Q407Q Substitution - coding silent 19:18668618-18668618 + C70 COSM4619479 c.1834G>A p.G612R Substitution - Missense 19:18669231-18669231 + WSU-HN6 COSM4596992 c.730G>C p.A244P Substitution - Missense 19:18668127-18668127 + B80-8 COSM1750735 c.976G>T p.V326F Substitution - Missense 19:18668373-18668373 + D10 COSM5007077 c.1102G>A p.G368R Substitution - Missense 19:18668499-18668499 + 424 COSM4432613 c.1783C>T p.P595S Substitution - Missense 19:18669180-18669180 + TCGA-BR-4201-01 COSM4075716 c.882G>A p.Q294Q Substitution - coding silent 19:18668279-18668279 + TCGA-BS-A0UV-01 COSM993130 c.360C>T p.F120F Substitution - coding silent 19:18667757-18667757 + HCC060T COSM5818037 c.1674G>A p.E558E Substitution - coding silent 19:18669071-18669071 + TCGA-BR-8382-01 COSM4075713 c.369C>T p.S123S Substitution - coding silent 19:18667766-18667766 + J30_T COSM3959734 c.1795G>T p.A599S Substitution - Missense 19:18669192-18669192 + TCGA-EJ-7791-01 COSM1471076 c.290G>A p.R97Q Substitution - Missense 19:18667687-18667687 + C135 COSM4617902 c.1689C>T p.I563I Substitution - coding silent 19:18669086-18669086 + ESCC_157 COSM5646323 c.243G>A p.L81L Substitution - coding silent 19:18664420-18664420 + BD72T COSM5513496 c.1732G>A p.V578I Substitution - Missense 19:18669129-18669129 + 2492720 COSM5722901 c.182A>T p.Q61L Substitution - Missense 19:18664359-18664359 + 8069332 COSM4406702 c.586G>A p.A196T Substitution - Missense 19:18667983-18667983 + SNU-C2B COSM4651353 c.934G>A p.V312I Substitution - Missense 19:18668331-18668331 + TCGA-GV-A3JW-01 COSM1304208 c.687G>A p.A229A Substitution - coding silent 19:18668084-18668084 + TCGA-G4-6298-01 COSM3692529 c.84-1G>A p.? Unknown 19:18664260-18664260 + TCGA-AZ-6601-01 COSM1391711 c.623G>A p.R208H Substitution - Missense 19:18668020-18668020 + T2940 COSM4696507 c.1693G>A p.G565R Substitution - Missense 19:18669090-18669090 + HRA19 COSM4637793 c.1251C>T p.A417A Substitution - coding silent 19:18668648-18668648 + TCGA-ER-A19J-06 COSM3530841 c.211A>G p.R71G Substitution - Missense 19:18664388-18664388 + TCGA-BR-8368-01 COSM4075720 c.1729A>G p.I577V Substitution - Missense 19:18669126-18669126 + tumor_4166151 COSM5948482 c.1162C>A p.P388T Substitution - Missense 19:18668559-18668559 + YUKAT COSM5389131 c.165C>T p.T55T Substitution - coding silent 19:18664342-18664342 + SW620 COSM4655773 c.1026C>T p.R342R Substitution - coding silent 19:18668423-18668423 + CCK81 COSM3100310 c.1576G>A p.V526M Substitution - Missense 19:18668973-18668973 + TCGA-AP-A0LM-01 COSM993131 c.1540G>A p.G514R Substitution - Missense 19:18668937-18668937 + TCGA-CG-5726-01 COSM4075719 c.1444G>A p.D482N Substitution - Missense 19:18668841-18668841 + PTC-7C COSM4131476 c.1708C>T p.R570C Substitution - Missense 19:18669105-18669105 + sysucc-882T COSM5447291 c.272T>C p.M91T Substitution - Missense 19:18667669-18667669 + 2334192 COSM312372 c.1471A>C p.K491Q Substitution - Missense 19:18668868-18668868 + 35M COSM5581491 c.773C>T p.S258L Substitution - Missense 19:18668170-18668170 + YUKAT COSM5389132 c.385G>A p.D129N Substitution - Missense 19:18667782-18667782 + LC_S19 COSM126766 c.862C>T p.Q288* Substitution - Nonsense 19:18668259-18668259 + TCGA-FS-A1ZZ-06 COSM3530846 c.1482G>A p.M494I Substitution - Missense 19:18668879-18668879 + TCGA-GM-A2DF-01 COSM3822366 c.1573G>A p.D525N Substitution - Missense 19:18668970-18668970 + pfg076T COSM4750695 c.1636C>T p.R546W Substitution - Missense 19:18669033-18669033 + HCC107 COSM1611841 c.690C>T p.A230A Substitution - coding silent 19:18668087-18668087 + TCGA-AA-3492-01 COSM1391707 c.160G>A p.A54T Substitution - Missense 19:18664337-18664337 + 2318502 COSM4777347 c.710A>C p.D237A Substitution - Missense 19:18668107-18668107 + MD-319 COSM302505 c.1623C>T p.S541S Substitution - coding silent 19:18669020-18669020 + 587234 COSM1212630 c.913C>T p.R305C Substitution - Missense 19:18668310-18668310 + B60 COSM1750733 c.426C>T p.F142F Substitution - coding silent 19:18667823-18667823 + ZZUFHECRKL-G021T COSM5442360 c.169C>T p.R57C Substitution - Missense 19:18664346-18664346 + OV207 COSM252571 c.1709G>A p.R570H Substitution - Missense 19:18669106-18669106 + 2492722 COSM5722901 c.182A>T p.Q61L Substitution - Missense 19:18664359-18664359 + TCGA-AZ-6598-01 COSM3692530 c.1307G>A p.R436Q Substitution - Missense 19:18668704-18668704 + HCC73T COSM1611842 c.1742A>G p.Y581C Substitution - Missense 19:18669139-18669139 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.250632 19p13.11 2476606|CGAP|BC026319|C/T|non-coding||3006|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.K491Q c.1471A>C 19 18779678 SCLC A G 3-UTRSNV . c.1845+1178A>G 19 18781230 HC A G Missense p.R71G c.211A>G 19 18775198 CM C A Synonymous p.P605P c.1815C>A 19 18780022 CM CC TT Missense p.R610W c.1827_1828delinsTT 19 18780034 CM C G Missense p.I117M c.351C>G 19 18778558 LUAD C G Missense p.S183W c.548C>G 19 18778755 RCCC C G Synonymous p.L36L c.108C>G 19 18775095 BRCA C T 3-UTRSNV . c.1845+14C>T 19 18780066 CM C T Missense p.R392C c.1174C>T 19 18779381 LUSC C T Nonsense p.Q288* c.862C>T 19 18779069 HNSC C T Synonymous p.F201F c.603C>T 19 18778810 CM C T Synonymous p.L62L c.186C>T 19 18775173 CM C T Synonymous p.T585T c.1755C>T 19 18779962 ESCA C T Synonymous p.Y442Y c.1326C>T 19 18779533 GBM G A IntronicSNV . c.84-9786G>A 19 18765285 CLL G A Missense p.A244T c.730G>A 19 18778937 STAD G A Missense p.D102N c.304G>A 19 18778511 CM G A Missense p.D482N c.1444G>A 19 18779651 STAD G A Missense p.M494I c.1482G>A 19 18779689 CM G A Missense p.R278H c.833G>A 19 18779040 OV G A Missense p.R97Q c.290G>A 19 18778497 PRAD G A Missense p.V499M c.1495G>A 19 18779702 LUSC G A Synonymous p.A158A c.474G>A 19 18778681 LUSC G A Synonymous p.A229A c.687G>A 19 18778894 BLCA G A Synonymous p.K475K c.1425G>A 19 18779632 CM G A Synonymous p.L156L c.468G>A 19 18778675 BRCA G A Synonymous p.Q294Q c.882G>A 19 18779089 STAD G A Synonymous p.T354T c.1062G>A 19 18779269 LGG GCGCG - Frameshift p.R243Qfs*91 c.726_730delGCGCG 19 18778933 RCCC G C Missense p.Q194H c.582G>C 19 18778789 HNSC G C Synonymous p.R190R c.570G>C 19 18778777 LUSC G - Frameshift p.Q369Sfs*22 c.1104delG 19 18779306 STAD G T Missense p.D237Y c.709G>T 19 18778916 LUAD G T Missense p.G108V c.323G>T 19 18778530 SCLC G T Missense p.G420C c.1258G>T 19 18779465 ESCA G T Missense p.V136L c.406G>T 19 18778613 LUSC