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 4 15613942 15613942 + Missense_Mutation SNP G G A TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr4:15613942G>A c.1946C>T c.(1945-1947)tCa>tTa p.S649L BLCA 4 15626988 15626988 + Silent SNP A A C TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr4:15626988A>C c.1737T>G c.(1735-1737)ccT>ccG p.P579P BLCA 4 15627442 15627442 + Missense_Mutation SNP G G A TCGA-XF-A9SM-01A-11D-A42E-08 TCGA-XF-A9SM-10A-01D-A42H-08 g.chr4:15627442G>A c.1283C>T c.(1282-1284)tCa>tTa p.S428L BLCA 4 15632388 15632388 + Missense_Mutation SNP C C T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr4:15632388C>T c.793G>A c.(793-795)Gaa>Aaa p.E265K BLCA 4 15646139 15646139 + Missense_Mutation SNP C C T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr4:15646139C>T c.277G>A c.(277-279)Gaa>Aaa p.E93K BLCA 4 15646174 15646174 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr4:15646174G>C c.242C>G c.(241-243)tCt>tGt p.S81C BRCA 4 15613942 15613942 + Nonsense_Mutation SNP G G C TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr4:15613942G>C c.1946C>G c.(1945-1947)tCa>tGa p.S649* BRCA 4 15627295 15627295 + Missense_Mutation SNP G G T TCGA-C8-A133-01A-32D-A12B-09 TCGA-C8-A133-10A-01D-A12B-09 g.chr4:15627295G>T c.1430C>A c.(1429-1431)cCt>cAt p.P477H BRCA 4 15629638 15629638 + Missense_Mutation SNP G G A TCGA-E9-A1RD-01A-11D-A159-09 TCGA-E9-A1RD-10A-01D-A159-09 g.chr4:15629638G>A c.911C>T c.(910-912)tCa>tTa p.S304L BRCA 4 15638232 15638232 + Silent SNP G G A TCGA-E2-A1IN-01A-11D-A13L-09 TCGA-E2-A1IN-10A-01D-A188-09 g.chr4:15638232G>A c.651C>T c.(649-651)ttC>ttT p.F217F BRCA 4 15640233 15640233 + Missense_Mutation SNP G G C TCGA-C8-A274-01A-11D-A16D-09 TCGA-C8-A274-10A-01D-A16D-09 g.chr4:15640233G>C c.481C>G c.(481-483)Cag>Gag p.Q161E BRCA 4 15642442 15642442 + Missense_Mutation SNP T T G TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr4:15642442T>G c.365A>C c.(364-366)gAt>gCt p.D122A CESC 4 15607356 15607356 + Missense_Mutation SNP G G C TCGA-EX-A1H6-01B-11D-A22X-09 TCGA-EX-A1H6-10A-01D-A22X-09 g.chr4:15607356G>C c.2066C>G c.(2065-2067)tCt>tGt p.S689C CESC 4 15607405 15607405 + Missense_Mutation SNP C C A TCGA-Q1-A73S-01A-11D-A33O-09 TCGA-Q1-A73S-10B-01D-A33O-09 g.chr4:15607405C>A c.2017G>T c.(2017-2019)Gcc>Tcc p.A673S COAD 4 15627568 15627568 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr4:15627568C>T c.1157G>A c.(1156-1158)cGg>cAg p.R386Q COAD 4 15638154 15638154 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr4:15638154C>T c.729G>A c.(727-729)tcG>tcA p.S243S COAD 4 15638225 15638225 + Missense_Mutation SNP G G C TCGA-DM-A0XF-01A-11D-A152-10 TCGA-DM-A0XF-10A-01D-A152-10 g.chr4:15638225G>C c.658C>G c.(658-660)Ctt>Gtt p.L220V COAD 4 15640297 15640297 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:15640297C>A c.417G>T c.(415-417)atG>atT p.M139I COADREAD 4 15627568 15627568 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr4:15627568C>T c.1157G>A c.(1156-1158)cGg>cAg p.R386Q COADREAD 4 15638154 15638154 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr4:15638154C>T c.729G>A c.(727-729)tcG>tcA p.S243S COADREAD 4 15638155 15638155 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:15638155G>A c.728C>T c.(727-729)tCg>tTg p.S243L COADREAD 4 15638225 15638225 + Missense_Mutation SNP G G C TCGA-DM-A0XF-01A-11D-A152-10 TCGA-DM-A0XF-10A-01D-A152-10 g.chr4:15638225G>C c.658C>G c.(658-660)Ctt>Gtt p.L220V COADREAD 4 15640297 15640297 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr4:15640297C>A c.417G>T c.(415-417)atG>atT p.M139I DLBC 4 15627092 15627092 + Missense_Mutation SNP A A G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr4:15627092A>G c.1633T>C c.(1633-1635)Tat>Cat p.Y545H ESCA 4 15638248 15638248 + Missense_Mutation SNP A A G TCGA-L5-A8NS-01A-12D-A37C-09 TCGA-L5-A8NS-11A-11D-A37F-09 g.chr4:15638248A>G c.635T>C c.(634-636)gTa>gCa p.V212A GBM 4 15626935 15626935 + Missense_Mutation SNP C C A TCGA-27-2528-01A-01D-1494-08 TCGA-27-2528-10A-01D-1494-08 g.chr4:15626935C>A c.1790G>T c.(1789-1791)gGa>gTa p.G597V GBM 4 15632339 15632339 + Missense_Mutation SNP T T G TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chr4:15632339T>G c.842A>C c.(841-843)gAa>gCa p.E281A GBMLGG 4 15626935 15626935 + Missense_Mutation SNP C C A TCGA-27-2528-01A-01D-1494-08 TCGA-27-2528-10A-01D-1494-08 g.chr4:15626935C>A c.1790G>T c.(1789-1791)gGa>gTa p.G597V GBMLGG 4 15632339 15632339 + Missense_Mutation SNP T T G TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chr4:15632339T>G c.842A>C c.(841-843)gAa>gCa p.E281A HNSC 4 15613901 15613901 + Missense_Mutation SNP C C T TCGA-TN-A7HJ-01A-12D-A34J-08 TCGA-TN-A7HJ-10A-01D-A34M-08 g.chr4:15613901C>T c.1987G>A c.(1987-1989)Gac>Aac p.D663N HNSC 4 15627093 15627093 + Silent SNP C C A TCGA-T2-A6WZ-01A-21D-A34J-08 TCGA-T2-A6WZ-10B-01D-A34M-08 g.chr4:15627093C>A c.1632G>T c.(1630-1632)gcG>gcT p.A544A HNSC 4 15627482 15627482 + Missense_Mutation SNP G G C TCGA-WA-A7H4-01A-21D-A34J-08 TCGA-WA-A7H4-10A-01D-A34M-08 g.chr4:15627482G>C c.1243C>G c.(1243-1245)Caa>Gaa p.Q415E HNSC 4 15632370 15632370 + Missense_Mutation SNP C C A TCGA-CR-6474-01A-11D-1870-08 TCGA-CR-6474-10A-01D-1870-08 g.chr4:15632370C>A c.811G>T c.(811-813)Gat>Tat p.D271Y KICH 4 15627587 15627587 + Missense_Mutation SNP C C A TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr4:15627587C>A c.1138G>T c.(1138-1140)Ggt>Tgt p.G380C KICH 4 15640143 15640143 + Missense_Mutation SNP T T C TCGA-KO-8414-01A-11D-2310-10 TCGA-KO-8414-11A-01D-2311-10 g.chr4:15640143T>C c.571A>G c.(571-573)Aag>Gag p.K191E KIPAN 4 15627587 15627587 + Missense_Mutation SNP C C A TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr4:15627587C>A c.1138G>T c.(1138-1140)Ggt>Tgt p.G380C KIPAN 4 15638133 15638133 + Silent SNP A A G TCGA-WN-AB4C-01A-11D-A42J-10 TCGA-WN-AB4C-10A-01D-A42M-10 g.chr4:15638133A>G c.750T>C c.(748-750)ccT>ccC p.P250P KIPAN 4 15640143 15640143 + Missense_Mutation SNP T T C TCGA-KO-8414-01A-11D-2310-10 TCGA-KO-8414-11A-01D-2311-10 g.chr4:15640143T>C c.571A>G c.(571-573)Aag>Gag p.K191E KIPAN 4 15640266 15640266 + Missense_Mutation SNP T T C TCGA-B9-5156-01A-01D-1589-08 TCGA-B9-5156-10A-01D-1589-08 g.chr4:15640266T>C c.448A>G c.(448-450)Att>Gtt p.I150V KIRP 4 15638133 15638133 + Silent SNP A A G TCGA-WN-AB4C-01A-11D-A42J-10 TCGA-WN-AB4C-10A-01D-A42M-10 g.chr4:15638133A>G c.750T>C c.(748-750)ccT>ccC p.P250P KIRP 4 15640266 15640266 + Missense_Mutation SNP T T C TCGA-B9-5156-01A-01D-1589-08 TCGA-B9-5156-10A-01D-1589-08 g.chr4:15640266T>C c.448A>G c.(448-450)Att>Gtt p.I150V LIHC 4 15627530 15627530 + Missense_Mutation SNP C C T TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr4:15627530C>T c.1195G>A c.(1195-1197)Gtg>Atg p.V399M LIHC 4 15629615 15629615 + Missense_Mutation SNP T T C TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chr4:15629615T>C c.934A>G c.(934-936)Atg>Gtg p.M312V LUAD 4 15627285 15627285 + Missense_Mutation SNP C C A TCGA-50-5066-01A-01D-1625-08 TCGA-50-5066-10A-01D-1625-08 g.chr4:15627285C>A c.1440G>T c.(1438-1440)tgG>tgT p.W480C LUAD 4 15627406 15627406 + Missense_Mutation SNP G G C TCGA-50-5066-01A-01D-1625-08 TCGA-50-5066-10A-01D-1625-08 g.chr4:15627406G>C c.1319C>G c.(1318-1320)tCc>tGc p.S440C LUAD 4 15627468 15627469 + Frame_Shift_Ins INS - - A TCGA-91-8496-01A-11D-2393-08 TCGA-91-8496-10A-01D-2393-08 g.chr4:15627468_15627469insA c.1256_1257insT c.(1255-1257)ttgfs p.L419fs LUAD 4 15646167 15646167 + Missense_Mutation SNP A A T TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr4:15646167A>T c.249T>A c.(247-249)aaT>aaA p.N83K LUSC 4 15627424 15627424 + Missense_Mutation SNP T T C TCGA-60-2724-01A-01D-1522-08 TCGA-60-2724-11A-01D-1522-08 g.chr4:15627424T>C c.1301A>G c.(1300-1302)aAa>aGa p.K434R OV 4 15627591 15627591 + Nonsense_Mutation SNP C C T TCGA-24-1842-01A-01W-0639-09 TCGA-24-1842-10A-01W-0639-09 g.chr4:15627591C>T c.1134G>A c.(1132-1134)tgG>tgA p.W378* OV 4 15628522 15628531 + Frame_Shift_Del DEL AGTCTGGGTA AGTCTGGGTA - TCGA-13-1498-01A-01W-0549-09 TCGA-13-1498-10A-01W-0549-09 g.chr4:15628522_15628531delAGTCTGGGTA c.1089_1098delTACCCAGACT c.(1087-1098)cttacccagactfs p.LTQT363fs PAAD 4 15627448 15627448 + Missense_Mutation SNP A A G TCGA-3E-AAAY-01A-11D-A38G-08 TCGA-3E-AAAY-10A-01D-A38J-08 g.chr4:15627448A>G c.1277T>C c.(1276-1278)aTt>aCt p.I426T PAAD 4 15628553 15628553 + Missense_Mutation SNP G G T TCGA-2L-AAQE-01A-11D-A397-08 TCGA-2L-AAQE-11A-11D-A39A-08 g.chr4:15628553G>T c.1067C>A c.(1066-1068)cCt>cAt p.P356H PAAD 4 15629518 15629518 + Missense_Mutation SNP G G C TCGA-OE-A75W-01A-12D-A32N-08 TCGA-OE-A75W-10A-01D-A32N-08 g.chr4:15629518G>C c.1031C>G c.(1030-1032)tCc>tGc p.S344C READ 4 15638155 15638155 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:15638155G>A c.728C>T c.(727-729)tCg>tTg p.S243L SKCM 4 15607372 15607372 + Nonsense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr4:15607372G>A c.2050C>T c.(2050-2052)Cga>Tga p.R684* SKCM 4 15614017 15614017 + Missense_Mutation SNP C C A TCGA-GN-A4U9-06A-11D-A32N-08 TCGA-GN-A4U9-10B-01D-A32N-08 g.chr4:15614017C>A c.1871G>T c.(1870-1872)gGg>gTg p.G624V SKCM 4 15627133 15627133 + Missense_Mutation SNP C C A TCGA-FS-A1ZM-06A-12D-A197-08 TCGA-FS-A1ZM-10A-01D-A199-08 g.chr4:15627133C>A c.1592G>T c.(1591-1593)aGt>aTt p.S531I SKCM 4 15640311 15640311 + Nonsense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr4:15640311G>A c.403C>T c.(403-405)Cag>Tag p.Q135*

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 4 15629497 15629497 single base substitution T C intron_variant BLCA-US 4 15601285 15601285 single base substitution G C downstream_gene_variant BLCA-US 4 15602891 15602891 single base substitution C G downstream_gene_variant BLCA-US 4 15626988 15626988 single base substitution A C 3_prime_UTR_variant BLCA-US 4 15626988 15626988 single base substitution A C exon_variant BLCA-US 4 15626988 15626988 single base substitution A C synonymous_variant P453P 1359T>G BLCA-US 4 15626988 15626988 single base substitution A C synonymous_variant P499P 1497T>G BLCA-US 4 15626988 15626988 single base substitution A C synonymous_variant P562P 1686T>G BLCA-US 4 15626988 15626988 single base substitution A C synonymous_variant P579P 1737T>G BOCA-FR 4 15666725 15666725 single base substitution C T intron_variant BRCA-EU 4 15601747 15601747 single base substitution A G downstream_gene_variant BRCA-EU 4 15602760 15602760 single base substitution G A downstream_gene_variant BRCA-EU 4 15605813 15605813 single base substitution C T downstream_gene_variant BRCA-EU 4 15607652 15607652 single base substitution A C intron_variant BRCA-EU 4 15609432 15609432 single base substitution G T downstream_gene_variant BRCA-EU 4 15609432 15609432 single base substitution G T intron_variant BRCA-EU 4 15610184 15610198 deletion of <=200bp GTGTCTACTCAGTGA - downstream_gene_variant BRCA-EU 4 15610184 15610198 deletion of <=200bp GTGTCTACTCAGTGA - intron_variant BRCA-EU 4 15610248 15610248 single base substitution G A downstream_gene_variant BRCA-EU 4 15610248 15610248 single base substitution G A intron_variant BRCA-EU 4 15611378 15611378 single base substitution A C downstream_gene_variant BRCA-EU 4 15611378 15611378 single base substitution A C intron_variant BRCA-EU 4 15611903 15611903 single base substitution G C downstream_gene_variant BRCA-EU 4 15611903 15611903 single base substitution G C intron_variant BRCA-EU 4 15614420 15614420 single base substitution C T intron_variant BRCA-EU 4 15614596 15614596 single base substitution G A intron_variant BRCA-EU 4 15616999 15616999 deletion of <=200bp C - intron_variant BRCA-EU 4 15617401 15617401 single base substitution A T intron_variant BRCA-EU 4 15618359 15618359 single base substitution A C intron_variant BRCA-EU 4 15618672 15618672 single base substitution G A intron_variant BRCA-EU 4 15618943 15618943 single base substitution C T intron_variant BRCA-EU 4 15620108 15620108 single base substitution C T intron_variant BRCA-EU 4 15620462 15620462 insertion of <=200bp - A intron_variant BRCA-EU 4 15620798 15620798 single base substitution C G intron_variant BRCA-EU 4 15620918 15620918 single base substitution A T intron_variant BRCA-EU 4 15622552 15622552 single base substitution G C intron_variant BRCA-EU 4 15626003 15626003 single base substitution G C intron_variant BRCA-EU 4 15628891 15628891 single base substitution G T intron_variant BRCA-EU 4 15631278 15631278 single base substitution G A intron_variant BRCA-EU 4 15631395 15631395 single base substitution G C intron_variant BRCA-EU 4 15632332 15632332 single base substitution A G 3_prime_UTR_variant BRCA-EU 4 15632332 15632332 single base substitution A G exon_variant BRCA-EU 4 15632332 15632332 single base substitution A G synonymous_variant R157R 471T>C BRCA-EU 4 15632332 15632332 single base substitution A G synonymous_variant R203R 609T>C BRCA-EU 4 15632332 15632332 single base substitution A G synonymous_variant R266R 798T>C BRCA-EU 4 15632332 15632332 single base substitution A G synonymous_variant R283R 849T>C BRCA-EU 4 15633279 15633279 single base substitution C G downstream_gene_variant BRCA-EU 4 15633279 15633279 single base substitution C G intron_variant BRCA-EU 4 15634253 15634253 single base substitution A G downstream_gene_variant BRCA-EU 4 15634253 15634253 single base substitution A G intron_variant BRCA-EU 4 15635579 15635579 single base substitution T A downstream_gene_variant BRCA-EU 4 15635579 15635579 single base substitution T A intron_variant BRCA-EU 4 15635766 15635766 single base substitution T A downstream_gene_variant BRCA-EU 4 15635766 15635766 single base substitution T A intron_variant BRCA-EU 4 15636636 15636644 deletion of <=200bp AAAATATCT - downstream_gene_variant BRCA-EU 4 15636636 15636644 deletion of <=200bp AAAATATCT - intron_variant BRCA-EU 4 15637319 15637319 single base substitution C T downstream_gene_variant BRCA-EU 4 15637319 15637319 single base substitution C T intron_variant BRCA-EU 4 15640615 15640615 single base substitution C T downstream_gene_variant BRCA-EU 4 15640615 15640615 single base substitution C T intron_variant BRCA-EU 4 15641046 15641046 single base substitution G A downstream_gene_variant BRCA-EU 4 15641046 15641046 single base substitution G A intron_variant BRCA-EU 4 15641530 15641530 single base substitution C A downstream_gene_variant BRCA-EU 4 15641530 15641530 single base substitution C A intron_variant BRCA-EU 4 15642217 15642217 single base substitution G T downstream_gene_variant BRCA-EU 4 15642217 15642217 single base substitution G T intron_variant BRCA-EU 4 15642497 15642497 single base substitution C T 3_prime_UTR_variant BRCA-EU 4 15642497 15642497 single base substitution C T 5_prime_UTR_variant BRCA-EU 4 15642497 15642497 single base substitution C T exon_variant BRCA-EU 4 15642497 15642497 single base substitution C T intron_variant BRCA-EU 4 15642497 15642497 single base substitution C T missense_variant E104K 310G>A BRCA-EU 4 15642497 15642497 single base substitution C T missense_variant E49K 145G>A BRCA-EU 4 15642497 15642497 single base substitution C T missense_variant E66K 196G>A BRCA-EU 4 15642497 15642497 single base substitution C T missense_variant E85K 253G>A BRCA-EU 4 15642497 15642497 single base substitution C T missense_variant E87K 259G>A BRCA-EU 4 15642604 15642604 deletion of <=200bp A - intron_variant BRCA-EU 4 15642976 15642976 single base substitution C T intron_variant BRCA-EU 4 15643542 15643542 single base substitution C T intron_variant BRCA-EU 4 15644597 15644597 single base substitution A T intron_variant BRCA-EU 4 15645812 15645812 single base substitution A G intron_variant BRCA-EU 4 15646722 15646722 single base substitution G A intron_variant BRCA-EU 4 15646722 15646722 single base substitution G A upstream_gene_variant BRCA-EU 4 15647060 15647060 deletion of <=200bp T - intron_variant BRCA-EU 4 15647060 15647060 deletion of <=200bp T - upstream_gene_variant BRCA-EU 4 15648087 15648087 single base substitution A G intron_variant BRCA-EU 4 15648087 15648087 single base substitution A G upstream_gene_variant BRCA-EU 4 15649607 15649607 single base substitution A T intron_variant BRCA-EU 4 15649607 15649607 single base substitution A T upstream_gene_variant BRCA-EU 4 15651062 15651062 single base substitution C T intron_variant BRCA-EU 4 15651062 15651062 single base substitution C T upstream_gene_variant BRCA-EU 4 15651138 15651138 single base substitution G C intron_variant BRCA-EU 4 15651138 15651138 single base substitution G C upstream_gene_variant BRCA-EU 4 15651532 15651532 single base substitution A T intron_variant BRCA-EU 4 15652021 15652021 single base substitution T C intron_variant BRCA-EU 4 15652929 15652929 deletion of <=200bp A - intron_variant BRCA-EU 4 15654094 15654094 deletion of <=200bp A - intron_variant BRCA-EU 4 15656219 15656219 single base substitution G A intron_variant BRCA-EU 4 15657115 15657115 single base substitution G A downstream_gene_variant BRCA-EU 4 15657115 15657115 single base substitution G A intron_variant BRCA-EU 4 15657115 15657115 single base substitution G A upstream_gene_variant BRCA-EU 4 15659762 15659762 single base substitution G A downstream_gene_variant BRCA-EU 4 15659762 15659762 single base substitution G A intron_variant BRCA-EU 4 15659762 15659762 single base substitution G A upstream_gene_variant BRCA-EU 4 15659935 15659935 single base substitution C T downstream_gene_variant BRCA-EU 4 15659935 15659935 single base substitution C T intron_variant BRCA-EU 4 15659935 15659935 single base substitution C T upstream_gene_variant BRCA-EU 4 15660895 15660896 deletion of <=200bp AA - downstream_gene_variant BRCA-EU 4 15660895 15660896 deletion of <=200bp AA - intron_variant BRCA-EU 4 15660895 15660896 deletion of <=200bp AA - upstream_gene_variant BRCA-EU 4 15661431 15661431 single base substitution G A 5_prime_UTR_variant BRCA-EU 4 15661431 15661431 single base substitution G A exon_variant BRCA-EU 4 15661431 15661431 single base substitution G A intron_variant BRCA-EU 4 15661431 15661431 single base substitution G A upstream_gene_variant BRCA-EU 4 15661611 15661611 single base substitution T C intron_variant BRCA-EU 4 15661611 15661611 single base substitution T C upstream_gene_variant BRCA-EU 4 15661994 15661994 single base substitution C T intron_variant BRCA-EU 4 15661994 15661994 single base substitution C T upstream_gene_variant BRCA-EU 4 15662533 15662533 single base substitution C G intron_variant BRCA-EU 4 15662533 15662533 single base substitution C G upstream_gene_variant BRCA-EU 4 15662901 15662901 single base substitution C G intron_variant BRCA-EU 4 15662901 15662901 single base substitution C G upstream_gene_variant BRCA-EU 4 15663115 15663115 single base substitution A G intron_variant BRCA-EU 4 15663115 15663115 single base substitution A G upstream_gene_variant BRCA-EU 4 15664398 15664398 deletion of <=200bp T - intron_variant BRCA-EU 4 15664398 15664398 deletion of <=200bp T - upstream_gene_variant BRCA-EU 4 15666203 15666203 single base substitution G A intron_variant BRCA-EU 4 15666203 15666203 single base substitution G A upstream_gene_variant BRCA-EU 4 15667648 15667648 single base substitution A T intron_variant BRCA-EU 4 15668062 15668062 single base substitution T C intron_variant BRCA-EU 4 15670085 15670085 deletion of <=200bp T - intron_variant BRCA-EU 4 15671156 15671156 deletion of <=200bp A - intron_variant BRCA-EU 4 15672181 15672181 single base substitution C A intron_variant BRCA-EU 4 15673373 15673373 deletion of <=200bp T - intron_variant BRCA-EU 4 15673571 15673571 single base substitution G C intron_variant BRCA-EU 4 15674474 15674474 single base substitution T C intron_variant BRCA-EU 4 15674623 15674623 single base substitution C T intron_variant BRCA-EU 4 15676463 15676463 single base substitution G A intron_variant BRCA-EU 4 15681103 15681103 single base substitution G T intron_variant BRCA-EU 4 15682382 15682382 single base substitution G C intron_variant BRCA-EU 4 15683522 15683522 single base substitution G C upstream_gene_variant BRCA-EU 4 15683780 15683780 single base substitution G A upstream_gene_variant BRCA-EU 4 15683793 15683793 single base substitution C T upstream_gene_variant BRCA-EU 4 15685219 15685219 single base substitution T A upstream_gene_variant BRCA-EU 4 15685807 15685807 single base substitution G A upstream_gene_variant BRCA-EU 4 15686703 15686703 single base substitution G C upstream_gene_variant BRCA-EU 4 15687162 15687162 single base substitution C T upstream_gene_variant BRCA-FR 4 15607652 15607652 single base substitution A C intron_variant BRCA-FR 4 15610248 15610248 single base substitution G A downstream_gene_variant BRCA-FR 4 15610248 15610248 single base substitution G A intron_variant BRCA-FR 4 15631278 15631278 single base substitution G A intron_variant BRCA-FR 4 15641530 15641530 single base substitution C A downstream_gene_variant BRCA-FR 4 15641530 15641530 single base substitution C A intron_variant BRCA-FR 4 15651138 15651138 single base substitution G C intron_variant BRCA-FR 4 15651138 15651138 single base substitution G C upstream_gene_variant BRCA-FR 4 15682382 15682382 single base substitution G C intron_variant BRCA-FR 4 15683793 15683793 single base substitution C T upstream_gene_variant BRCA-FR 4 15685807 15685807 single base substitution G A upstream_gene_variant BRCA-KR 4 15602858 15602858 single base substitution A G downstream_gene_variant BRCA-KR 4 15628514 15628514 single base substitution G A 3_prime_UTR_variant BRCA-KR 4 15628514 15628514 single base substitution G A exon_variant BRCA-KR 4 15628514 15628514 single base substitution G A missense_variant S243L 728C>T BRCA-KR 4 15628514 15628514 single base substitution G A missense_variant S289L 866C>T BRCA-KR 4 15628514 15628514 single base substitution G A missense_variant S352L 1055C>T BRCA-KR 4 15628514 15628514 single base substitution G A missense_variant S369L 1106C>T BRCA-UK 4 15602875 15602875 single base substitution C G downstream_gene_variant BRCA-UK 4 15609825 15609825 single base substitution C T downstream_gene_variant BRCA-UK 4 15609825 15609825 single base substitution C T intron_variant BRCA-UK 4 15617401 15617401 single base substitution A T intron_variant BRCA-UK 4 15663413 15663413 single base substitution C T intron_variant BRCA-UK 4 15663413 15663413 single base substitution C T upstream_gene_variant BRCA-US 4 15613942 15613942 single base substitution G C 3_prime_UTR_variant BRCA-US 4 15613942 15613942 single base substitution G C exon_variant BRCA-US 4 15613942 15613942 single base substitution G C stop_gained S523* 1568C>G BRCA-US 4 15613942 15613942 single base substitution G C stop_gained S569* 1706C>G BRCA-US 4 15613942 15613942 single base substitution G C stop_gained S632* 1895C>G BRCA-US 4 15613942 15613942 single base substitution G C stop_gained S649* 1946C>G BRCA-US 4 15627295 15627295 single base substitution G T 3_prime_UTR_variant BRCA-US 4 15627295 15627295 single base substitution G T exon_variant BRCA-US 4 15627295 15627295 single base substitution G T missense_variant P351H 1052C>A BRCA-US 4 15627295 15627295 single base substitution G T missense_variant P397H 1190C>A BRCA-US 4 15627295 15627295 single base substitution G T missense_variant P460H 1379C>A BRCA-US 4 15627295 15627295 single base substitution G T missense_variant P477H 1430C>A BRCA-US 4 15629638 15629638 single base substitution G A 3_prime_UTR_variant BRCA-US 4 15629638 15629638 single base substitution G A exon_variant BRCA-US 4 15629638 15629638 single base substitution G A missense_variant S178L 533C>T BRCA-US 4 15629638 15629638 single base substitution G A missense_variant S224L 671C>T BRCA-US 4 15629638 15629638 single base substitution G A missense_variant S287L 860C>T BRCA-US 4 15629638 15629638 single base substitution G A missense_variant S304L 911C>T BRCA-US 4 15638232 15638232 single base substitution G A 3_prime_UTR_variant BRCA-US 4 15638232 15638232 single base substitution G A downstream_gene_variant BRCA-US 4 15638232 15638232 single base substitution G A exon_variant BRCA-US 4 15638232 15638232 single base substitution G A synonymous_variant F137F 411C>T BRCA-US 4 15638232 15638232 single base substitution G A synonymous_variant F177F 531C>T BRCA-US 4 15638232 15638232 single base substitution G A synonymous_variant F200F 600C>T BRCA-US 4 15638232 15638232 single base substitution G A synonymous_variant F217F 651C>T BRCA-US 4 15638232 15638232 single base substitution G A synonymous_variant F91F 273C>T BRCA-US 4 15640233 15640233 single base substitution G C 3_prime_UTR_variant BRCA-US 4 15640233 15640233 single base substitution G C downstream_gene_variant BRCA-US 4 15640233 15640233 single base substitution G C exon_variant BRCA-US 4 15640233 15640233 single base substitution G C missense_variant Q106E 316C>G BRCA-US 4 15640233 15640233 single base substitution G C missense_variant Q123E 367C>G BRCA-US 4 15640233 15640233 single base substitution G C missense_variant Q144E 430C>G BRCA-US 4 15640233 15640233 single base substitution G C missense_variant Q161E 481C>G BRCA-US 4 15640233 15640233 single base substitution G C missense_variant Q35E 103C>G BRCA-US 4 15640233 15640233 single base substitution G C missense_variant Q81E 241C>G BRCA-US 4 15642442 15642442 single base substitution T G 3_prime_UTR_variant BRCA-US 4 15642442 15642442 single base substitution T G 5_prime_UTR_variant BRCA-US 4 15642442 15642442 single base substitution T G downstream_gene_variant BRCA-US 4 15642442 15642442 single base substitution T G exon_variant BRCA-US 4 15642442 15642442 single base substitution T G intron_variant BRCA-US 4 15642442 15642442 single base substitution T G missense_variant D105A 314A>C BRCA-US 4 15642442 15642442 single base substitution T G missense_variant D122A 365A>C BRCA-US 4 15642442 15642442 single base substitution T G missense_variant D67A 200A>C BRCA-US 4 15642442 15642442 single base substitution T G missense_variant D84A 251A>C BTCA-JP 4 15601178 15601178 single base substitution T A downstream_gene_variant BTCA-JP 4 15638151 15638151 single base substitution A G 3_prime_UTR_variant BTCA-JP 4 15638151 15638151 single base substitution A G downstream_gene_variant BTCA-JP 4 15638151 15638151 single base substitution A G exon_variant BTCA-JP 4 15638151 15638151 single base substitution A G synonymous_variant L118L 354T>C BTCA-JP 4 15638151 15638151 single base substitution A G synonymous_variant L164L 492T>C BTCA-JP 4 15638151 15638151 single base substitution A G synonymous_variant L227L 681T>C BTCA-JP 4 15638151 15638151 single base substitution A G synonymous_variant L244L 732T>C CESC-US 4 15607356 15607356 single base substitution G C 3_prime_UTR_variant CESC-US 4 15607356 15607356 single base substitution G C missense_variant S563C 1688C>G CESC-US 4 15607356 15607356 single base substitution G C missense_variant S609C 1826C>G CESC-US 4 15607356 15607356 single base substitution G C missense_variant S672C 2015C>G CESC-US 4 15607356 15607356 single base substitution G C missense_variant S689C 2066C>G CESC-US 4 15607405 15607405 single base substitution C A 3_prime_UTR_variant CESC-US 4 15607405 15607405 single base substitution C A missense_variant A547S 1639G>T CESC-US 4 15607405 15607405 single base substitution C A missense_variant A593S 1777G>T CESC-US 4 15607405 15607405 single base substitution C A missense_variant A656S 1966G>T CESC-US 4 15607405 15607405 single base substitution C A missense_variant A673S 2017G>T CESC-US 4 15687994 15687994 single base substitution G C upstream_gene_variant CLLE-ES 4 15615214 15615214 single base substitution T G intron_variant CLLE-ES 4 15627718 15627718 single base substitution T A intron_variant CLLE-ES 4 15631000 15631000 single base substitution T A intron_variant CLLE-ES 4 15664083 15664083 single base substitution G T intron_variant CLLE-ES 4 15664083 15664083 single base substitution G T upstream_gene_variant CLLE-ES 4 15674764 15674764 single base substitution A G intron_variant CLLE-ES 4 15674787 15674787 single base substitution A C intron_variant CLLE-ES 4 15687638 15687638 single base substitution T C upstream_gene_variant COAD-US 4 15602885 15602885 single base substitution C T downstream_gene_variant COAD-US 4 15638225 15638225 single base substitution G C 3_prime_UTR_variant COAD-US 4 15638225 15638225 single base substitution G C downstream_gene_variant COAD-US 4 15638225 15638225 single base substitution G C exon_variant COAD-US 4 15638225 15638225 single base substitution G C missense_variant L140V 418C>G COAD-US 4 15638225 15638225 single base substitution G C missense_variant L180V 538C>G COAD-US 4 15638225 15638225 single base substitution G C missense_variant L203V 607C>G COAD-US 4 15638225 15638225 single base substitution G C missense_variant L220V 658C>G COAD-US 4 15638225 15638225 single base substitution G C missense_variant L94V 280C>G COAD-US 4 15640297 15640297 single base substitution C A 3_prime_UTR_variant COAD-US 4 15640297 15640297 single base substitution C A downstream_gene_variant COAD-US 4 15640297 15640297 single base substitution C A exon_variant COAD-US 4 15640297 15640297 single base substitution C A missense_variant M101I 303G>T COAD-US 4 15640297 15640297 single base substitution C A missense_variant M122I 366G>T COAD-US 4 15640297 15640297 single base substitution C A missense_variant M139I 417G>T COAD-US 4 15640297 15640297 single base substitution C A missense_variant M13I 39G>T COAD-US 4 15640297 15640297 single base substitution C A missense_variant M59I 177G>T COAD-US 4 15640297 15640297 single base substitution C A missense_variant M84I 252G>T COCA-CN 4 15601212 15601212 single base substitution G A downstream_gene_variant COCA-CN 4 15601245 15601245 single base substitution C A downstream_gene_variant COCA-CN 4 15602818 15602818 single base substitution C A downstream_gene_variant COCA-CN 4 15646089 15646089 single base substitution A G intron_variant EOPC-DE 4 15648469 15648469 single base substitution T G intron_variant EOPC-DE 4 15648469 15648469 single base substitution T G upstream_gene_variant EOPC-DE 4 15686456 15686456 single base substitution G T upstream_gene_variant ESAD-UK 4 15605706 15605706 single base substitution C A downstream_gene_variant ESAD-UK 4 15605856 15605856 single base substitution C T downstream_gene_variant ESAD-UK 4 15608660 15608660 single base substitution A T downstream_gene_variant ESAD-UK 4 15608660 15608660 single base substitution A T intron_variant ESAD-UK 4 15613842 15613842 single base substitution T A exon_variant ESAD-UK 4 15613842 15613842 single base substitution T A intron_variant ESAD-UK 4 15615471 15615471 single base substitution T G intron_variant ESAD-UK 4 15619477 15619477 single base substitution A G intron_variant ESAD-UK 4 15619606 15619606 deletion of <=200bp A - intron_variant ESAD-UK 4 15620462 15620462 deletion of <=200bp A - intron_variant ESAD-UK 4 15621045 15621045 insertion of <=200bp - A intron_variant ESAD-UK 4 15621090 15621090 deletion of <=200bp C - intron_variant ESAD-UK 4 15621214 15621214 insertion of <=200bp - A intron_variant ESAD-UK 4 15621804 15621804 single base substitution C A intron_variant ESAD-UK 4 15622787 15622787 single base substitution A C intron_variant ESAD-UK 4 15625452 15625452 single base substitution T A intron_variant ESAD-UK 4 15629420 15629420 single base substitution T G intron_variant ESAD-UK 4 15630562 15630562 insertion of <=200bp - T intron_variant ESAD-UK 4 15635505 15635505 single base substitution G A downstream_gene_variant ESAD-UK 4 15635505 15635505 single base substitution G A intron_variant ESAD-UK 4 15636082 15636082 single base substitution G A downstream_gene_variant ESAD-UK 4 15636082 15636082 single base substitution G A intron_variant ESAD-UK 4 15637503 15637503 single base substitution T C downstream_gene_variant ESAD-UK 4 15637503 15637503 single base substitution T C intron_variant ESAD-UK 4 15642695 15642695 single base substitution T C intron_variant ESAD-UK 4 15643000 15643000 single base substitution C A intron_variant ESAD-UK 4 15643750 15643750 single base substitution T C intron_variant ESAD-UK 4 15644161 15644161 single base substitution T G intron_variant ESAD-UK 4 15646583 15646583 single base substitution G A intron_variant ESAD-UK 4 15646583 15646583 single base substitution G A upstream_gene_variant ESAD-UK 4 15648086 15648086 single base substitution A G intron_variant ESAD-UK 4 15648086 15648086 single base substitution A G upstream_gene_variant ESAD-UK 4 15648087 15648087 single base substitution A G intron_variant ESAD-UK 4 15648087 15648087 single base substitution A G upstream_gene_variant ESAD-UK 4 15652217 15652217 single base substitution G A intron_variant ESAD-UK 4 15657461 15657461 single base substitution C A downstream_gene_variant ESAD-UK 4 15657461 15657461 single base substitution C A intron_variant ESAD-UK 4 15657461 15657461 single base substitution C A upstream_gene_variant ESAD-UK 4 15657933 15657933 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 4 15657933 15657933 single base substitution C A downstream_gene_variant ESAD-UK 4 15657933 15657933 single base substitution C A intron_variant ESAD-UK 4 15657933 15657933 single base substitution C A upstream_gene_variant ESAD-UK 4 15657933 15657933 single base substitution C T 5_prime_UTR_variant ESAD-UK 4 15657933 15657933 single base substitution C T downstream_gene_variant ESAD-UK 4 15657933 15657933 single base substitution C T intron_variant ESAD-UK 4 15657933 15657933 single base substitution C T upstream_gene_variant ESAD-UK 4 15660264 15660264 single base substitution G A downstream_gene_variant ESAD-UK 4 15660264 15660264 single base substitution G A intron_variant ESAD-UK 4 15660264 15660264 single base substitution G A upstream_gene_variant ESAD-UK 4 15663256 15663256 insertion of <=200bp - T intron_variant ESAD-UK 4 15663256 15663256 insertion of <=200bp - T upstream_gene_variant ESAD-UK 4 15665223 15665223 single base substitution C A intron_variant ESAD-UK 4 15665223 15665223 single base substitution C A upstream_gene_variant ESAD-UK 4 15667648 15667648 single base substitution A T intron_variant ESAD-UK 4 15673001 15673001 single base substitution A G intron_variant ESAD-UK 4 15673401 15673401 single base substitution T C intron_variant ESAD-UK 4 15675406 15675406 single base substitution A G intron_variant ESAD-UK 4 15677782 15677782 single base substitution A G intron_variant ESAD-UK 4 15678510 15678510 single base substitution T G intron_variant ESAD-UK 4 15680563 15680563 single base substitution C A intron_variant ESAD-UK 4 15682870 15682870 single base substitution C T intron_variant ESAD-UK 4 15683970 15683970 single base substitution T C upstream_gene_variant ESAD-UK 4 15684572 15684572 single base substitution A G upstream_gene_variant ESCA-CN 4 15627353 15627353 single base substitution C T 3_prime_UTR_variant ESCA-CN 4 15627353 15627353 single base substitution C T exon_variant ESCA-CN 4 15627353 15627353 single base substitution C T missense_variant E332K 994G>A ESCA-CN 4 15627353 15627353 single base substitution C T missense_variant E378K 1132G>A ESCA-CN 4 15627353 15627353 single base substitution C T missense_variant E441K 1321G>A ESCA-CN 4 15627353 15627353 single base substitution C T missense_variant E458K 1372G>A GBM-US 4 15626935 15626935 single base substitution C A 3_prime_UTR_variant GBM-US 4 15626935 15626935 single base substitution C A exon_variant GBM-US 4 15626935 15626935 single base substitution C A missense_variant G471V 1412G>T GBM-US 4 15626935 15626935 single base substitution C A missense_variant G517V 1550G>T GBM-US 4 15626935 15626935 single base substitution C A missense_variant G580V 1739G>T GBM-US 4 15626935 15626935 single base substitution C A missense_variant G597V 1790G>T GBM-US 4 15632339 15632339 single base substitution T G 3_prime_UTR_variant GBM-US 4 15632339 15632339 single base substitution T G exon_variant GBM-US 4 15632339 15632339 single base substitution T G missense_variant E155A 464A>C GBM-US 4 15632339 15632339 single base substitution T G missense_variant E201A 602A>C GBM-US 4 15632339 15632339 single base substitution T G missense_variant E264A 791A>C GBM-US 4 15632339 15632339 single base substitution T G missense_variant E281A 842A>C KIRP-US 4 15640266 15640266 single base substitution T C 3_prime_UTR_variant KIRP-US 4 15640266 15640266 single base substitution T C downstream_gene_variant KIRP-US 4 15640266 15640266 single base substitution T C exon_variant KIRP-US 4 15640266 15640266 single base substitution T C missense_variant I112V 334A>G KIRP-US 4 15640266 15640266 single base substitution T C missense_variant I133V 397A>G KIRP-US 4 15640266 15640266 single base substitution T C missense_variant I150V 448A>G KIRP-US 4 15640266 15640266 single base substitution T C missense_variant I24V 70A>G KIRP-US 4 15640266 15640266 single base substitution T C missense_variant I70V 208A>G KIRP-US 4 15640266 15640266 single base substitution T C missense_variant I95V 283A>G LAML-KR 4 15603069 15603069 single base substitution G C downstream_gene_variant LICA-CN 4 15601278 15601278 single base substitution T A downstream_gene_variant LICA-CN 4 15613901 15613901 single base substitution C A 3_prime_UTR_variant LICA-CN 4 15613901 15613901 single base substitution C A exon_variant LICA-CN 4 15613901 15613901 single base substitution C A missense_variant D537Y 1609G>T LICA-CN 4 15613901 15613901 single base substitution C A missense_variant D583Y 1747G>T LICA-CN 4 15613901 15613901 single base substitution C A missense_variant D646Y 1936G>T LICA-CN 4 15613901 15613901 single base substitution C A missense_variant D663Y 1987G>T LICA-FR 4 15613867 15613867 single base substitution T C exon_variant LICA-FR 4 15613867 15613867 single base substitution T C intron_variant LICA-FR 4 15613973 15613973 single base substitution T C 3_prime_UTR_variant LICA-FR 4 15613973 15613973 single base substitution T C exon_variant LICA-FR 4 15613973 15613973 single base substitution T C missense_variant I513V 1537A>G LICA-FR 4 15613973 15613973 single base substitution T C missense_variant I559V 1675A>G LICA-FR 4 15613973 15613973 single base substitution T C missense_variant I622V 1864A>G LICA-FR 4 15613973 15613973 single base substitution T C missense_variant I639V 1915A>G LICA-FR 4 15617012 15617012 single base substitution G A intron_variant LICA-FR 4 15617042 15617042 single base substitution G A intron_variant LICA-FR 4 15617045 15617045 single base substitution A T intron_variant LICA-FR 4 15622414 15622422 deletion of <=200bp AGGGCGGAA - intron_variant LICA-FR 4 15628504 15628504 single base substitution T A 3_prime_UTR_variant LICA-FR 4 15628504 15628504 single base substitution T A exon_variant LICA-FR 4 15628504 15628504 single base substitution T A synonymous_variant A246A 738A>T LICA-FR 4 15628504 15628504 single base substitution T A synonymous_variant A292A 876A>T LICA-FR 4 15628504 15628504 single base substitution T A synonymous_variant A355A 1065A>T LICA-FR 4 15628504 15628504 single base substitution T A synonymous_variant A372A 1116A>T LIHC-US 4 15601277 15601277 single base substitution A G downstream_gene_variant LIHC-US 4 15629615 15629615 single base substitution T C 3_prime_UTR_variant LIHC-US 4 15629615 15629615 single base substitution T C exon_variant LIHC-US 4 15629615 15629615 single base substitution T C missense_variant M186V 556A>G LIHC-US 4 15629615 15629615 single base substitution T C missense_variant M232V 694A>G LIHC-US 4 15629615 15629615 single base substitution T C missense_variant M295V 883A>G LIHC-US 4 15629615 15629615 single base substitution T C missense_variant M312V 934A>G LINC-JP 4 15601182 15601182 single base substitution G T downstream_gene_variant LINC-JP 4 15602670 15602670 single base substitution T C downstream_gene_variant LINC-JP 4 15603049 15603049 single base substitution T G downstream_gene_variant LINC-JP 4 15603066 15603066 single base substitution T C downstream_gene_variant LINC-JP 4 15605869 15605869 single base substitution C A downstream_gene_variant LINC-JP 4 15607532 15607532 insertion of <=200bp - A intron_variant LINC-JP 4 15612346 15612346 single base substitution C A downstream_gene_variant LINC-JP 4 15612346 15612346 single base substitution C A intron_variant LINC-JP 4 15613977 15613977 insertion of <=200bp - A 3_prime_UTR_variant LINC-JP 4 15613977 15613977 insertion of <=200bp - A exon_variant LINC-JP 4 15613977 15613977 insertion of <=200bp - A frameshift_variant L511L? LINC-JP 4 15613977 15613977 insertion of <=200bp - A frameshift_variant L557L? LINC-JP 4 15613977 15613977 insertion of <=200bp - A frameshift_variant L620L? LINC-JP 4 15613977 15613977 insertion of <=200bp - A frameshift_variant L637L? LINC-JP 4 15619053 15619053 single base substitution C A intron_variant LINC-JP 4 15625386 15625386 single base substitution C T intron_variant LINC-JP 4 15627042 15627042 single base substitution T C 3_prime_UTR_variant LINC-JP 4 15627042 15627042 single base substitution T C exon_variant LINC-JP 4 15627042 15627042 single base substitution T C synonymous_variant S435S 1305A>G LINC-JP 4 15627042 15627042 single base substitution T C synonymous_variant S481S 1443A>G LINC-JP 4 15627042 15627042 single base substitution T C synonymous_variant S544S 1632A>G LINC-JP 4 15627042 15627042 single base substitution T C synonymous_variant S561S 1683A>G LINC-JP 4 15627981 15627981 single base substitution T A intron_variant LINC-JP 4 15638592 15638592 single base substitution T C downstream_gene_variant LINC-JP 4 15638592 15638592 single base substitution T C intron_variant LINC-JP 4 15642249 15642249 deletion of <=200bp T - downstream_gene_variant LINC-JP 4 15642249 15642249 deletion of <=200bp T - intron_variant LINC-JP 4 15646469 15646469 single base substitution T C intron_variant LINC-JP 4 15646469 15646469 single base substitution T C upstream_gene_variant LINC-JP 4 15657742 15657742 single base substitution C A downstream_gene_variant LINC-JP 4 15657742 15657742 single base substitution C A intron_variant LINC-JP 4 15657742 15657742 single base substitution C A upstream_gene_variant LINC-JP 4 15679726 15679726 single base substitution A T intron_variant LINC-JP 4 15685265 15685265 single base substitution C G upstream_gene_variant LIRI-JP 4 15601753 15601753 single base substitution T C downstream_gene_variant LIRI-JP 4 15601908 15601908 single base substitution C T downstream_gene_variant LIRI-JP 4 15602813 15602818 deletion of <=200bp TAAATC - downstream_gene_variant LIRI-JP 4 15606447 15606447 single base substitution T C 3_prime_UTR_variant LIRI-JP 4 15606447 15606447 single base substitution T C downstream_gene_variant LIRI-JP 4 15606661 15606661 single base substitution T C 3_prime_UTR_variant LIRI-JP 4 15607444 15607444 single base substitution T A intron_variant LIRI-JP 4 15608114 15608114 single base substitution T C intron_variant LIRI-JP 4 15608339 15608339 single base substitution A T intron_variant LIRI-JP 4 15608480 15608480 single base substitution T C intron_variant LIRI-JP 4 15609558 15609558 single base substitution T C downstream_gene_variant LIRI-JP 4 15609558 15609558 single base substitution T C intron_variant LIRI-JP 4 15612645 15612645 single base substitution T G downstream_gene_variant LIRI-JP 4 15612645 15612645 single base substitution T G intron_variant LIRI-JP 4 15618667 15618667 single base substitution T C intron_variant LIRI-JP 4 15619215 15619215 single base substitution A C intron_variant LIRI-JP 4 15621481 15621481 single base substitution T C intron_variant LIRI-JP 4 15622979 15622979 single base substitution T C intron_variant LIRI-JP 4 15623265 15623265 single base substitution T C intron_variant LIRI-JP 4 15624136 15624136 single base substitution T C intron_variant LIRI-JP 4 15624434 15624434 single base substitution G T intron_variant LIRI-JP 4 15625016 15625016 single base substitution C A intron_variant LIRI-JP 4 15629042 15629042 single base substitution C T intron_variant LIRI-JP 4 15629499 15629499 single base substitution T C intron_variant LIRI-JP 4 15629709 15629709 single base substitution C T intron_variant LIRI-JP 4 15630477 15630477 single base substitution A C intron_variant LIRI-JP 4 15631805 15631805 single base substitution T A intron_variant LIRI-JP 4 15632695 15632695 single base substitution C T intron_variant LIRI-JP 4 15633734 15633734 single base substitution T C downstream_gene_variant LIRI-JP 4 15633734 15633734 single base substitution T C intron_variant LIRI-JP 4 15634383 15634383 single base substitution C A downstream_gene_variant LIRI-JP 4 15634383 15634383 single base substitution C A intron_variant LIRI-JP 4 15634803 15634803 single base substitution C G downstream_gene_variant LIRI-JP 4 15634803 15634803 single base substitution C G intron_variant LIRI-JP 4 15635353 15635353 single base substitution T C downstream_gene_variant LIRI-JP 4 15635353 15635353 single base substitution T C intron_variant LIRI-JP 4 15635802 15635802 single base substitution C T downstream_gene_variant LIRI-JP 4 15635802 15635802 single base substitution C T intron_variant LIRI-JP 4 15640764 15640764 single base substitution G T downstream_gene_variant LIRI-JP 4 15640764 15640764 single base substitution G T intron_variant LIRI-JP 4 15640936 15640936 single base substitution A G downstream_gene_variant LIRI-JP 4 15640936 15640936 single base substitution A G intron_variant LIRI-JP 4 15641004 15641004 single base substitution T C downstream_gene_variant LIRI-JP 4 15641004 15641004 single base substitution T C intron_variant LIRI-JP 4 15646599 15646599 single base substitution A C intron_variant LIRI-JP 4 15646599 15646599 single base substitution A C upstream_gene_variant LIRI-JP 4 15649338 15649338 single base substitution C T intron_variant LIRI-JP 4 15649338 15649338 single base substitution C T upstream_gene_variant LIRI-JP 4 15650255 15650255 single base substitution T C intron_variant LIRI-JP 4 15650255 15650255 single base substitution T C upstream_gene_variant LIRI-JP 4 15650769 15650769 single base substitution A G intron_variant LIRI-JP 4 15650769 15650769 single base substitution A G upstream_gene_variant LIRI-JP 4 15652903 15652903 single base substitution G T intron_variant LIRI-JP 4 15654156 15654156 single base substitution C A intron_variant LIRI-JP 4 15654313 15654313 single base substitution T C intron_variant LIRI-JP 4 15655372 15655406 deletion of <=200bp ATATACCCTCTTGCTTAATGGCTTAACCATTCCTC - intron_variant LIRI-JP 4 15655438 15655438 single base substitution C A intron_variant LIRI-JP 4 15657692 15657692 single base substitution G A downstream_gene_variant LIRI-JP 4 15657692 15657692 single base substitution G A intron_variant LIRI-JP 4 15657692 15657692 single base substitution G A upstream_gene_variant LIRI-JP 4 15658112 15658112 single base substitution A G downstream_gene_variant LIRI-JP 4 15658112 15658112 single base substitution A G intron_variant LIRI-JP 4 15658112 15658112 single base substitution A G upstream_gene_variant LIRI-JP 4 15662618 15662618 single base substitution T G intron_variant LIRI-JP 4 15662618 15662618 single base substitution T G upstream_gene_variant LIRI-JP 4 15663538 15663538 single base substitution C A intron_variant LIRI-JP 4 15663538 15663538 single base substitution C A upstream_gene_variant LIRI-JP 4 15671213 15671213 single base substitution T A intron_variant LIRI-JP 4 15675392 15675392 single base substitution C G intron_variant LIRI-JP 4 15676879 15676879 single base substitution A G intron_variant LIRI-JP 4 15678758 15678758 single base substitution T C intron_variant LIRI-JP 4 15679257 15679257 single base substitution G A intron_variant LIRI-JP 4 15680501 15680501 single base substitution T A intron_variant LIRI-JP 4 15680549 15680549 single base substitution T C intron_variant LIRI-JP 4 15681727 15681727 single base substitution T C intron_variant LIRI-JP 4 15685915 15685915 single base substitution A G upstream_gene_variant LIRI-JP 4 15685958 15685958 single base substitution G T upstream_gene_variant LIRI-JP 4 15687436 15687436 deletion of <=200bp A - upstream_gene_variant LIRI-JP 4 15687657 15687657 single base substitution T C upstream_gene_variant LIRI-JP 4 15688055 15688055 single base substitution T G upstream_gene_variant LUSC-KR 4 15605363 15605363 single base substitution T A downstream_gene_variant LUSC-KR 4 15612687 15612687 single base substitution C T downstream_gene_variant LUSC-KR 4 15612687 15612687 single base substitution C T intron_variant LUSC-KR 4 15619454 15619454 single base substitution G A intron_variant LUSC-KR 4 15627675 15627675 single base substitution G A intron_variant LUSC-KR 4 15628362 15628362 single base substitution G A intron_variant LUSC-KR 4 15636895 15636895 single base substitution G T downstream_gene_variant LUSC-KR 4 15636895 15636895 single base substitution G T intron_variant LUSC-KR 4 15638910 15638910 single base substitution G T downstream_gene_variant LUSC-KR 4 15638910 15638910 single base substitution G T intron_variant LUSC-KR 4 15645800 15645800 single base substitution G A intron_variant LUSC-KR 4 15657115 15657115 single base substitution G C downstream_gene_variant LUSC-KR 4 15657115 15657115 single base substitution G C intron_variant LUSC-KR 4 15657115 15657115 single base substitution G C upstream_gene_variant LUSC-KR 4 15665631 15665631 single base substitution G C intron_variant LUSC-KR 4 15665631 15665631 single base substitution G C upstream_gene_variant LUSC-KR 4 15680612 15680612 single base substitution G A intron_variant LUSC-KR 4 15682933 15682933 single base substitution C T 5_prime_UTR_variant LUSC-KR 4 15682933 15682933 single base substitution C T exon_variant LUSC-KR 4 15682933 15682933 single base substitution C T intron_variant LUSC-KR 4 15685951 15685951 single base substitution C G upstream_gene_variant LUSC-US 4 15627424 15627424 single base substitution T C 3_prime_UTR_variant LUSC-US 4 15627424 15627424 single base substitution T C exon_variant LUSC-US 4 15627424 15627424 single base substitution T C missense_variant K308R 923A>G LUSC-US 4 15627424 15627424 single base substitution T C missense_variant K354R 1061A>G LUSC-US 4 15627424 15627424 single base substitution T C missense_variant K417R 1250A>G LUSC-US 4 15627424 15627424 single base substitution T C missense_variant K434R 1301A>G MALY-DE 4 15603037 15603037 single base substitution C T downstream_gene_variant MALY-DE 4 15609785 15609787 deletion of <=200bp TAT - downstream_gene_variant MALY-DE 4 15609785 15609787 deletion of <=200bp TAT - intron_variant MALY-DE 4 15627274 15627274 single base substitution G C 3_prime_UTR_variant MALY-DE 4 15627274 15627274 single base substitution G C exon_variant MALY-DE 4 15627274 15627274 single base substitution G C missense_variant A358G 1073C>G MALY-DE 4 15627274 15627274 single base substitution G C missense_variant A404G 1211C>G MALY-DE 4 15627274 15627274 single base substitution G C missense_variant A467G 1400C>G MALY-DE 4 15627274 15627274 single base substitution G C missense_variant A484G 1451C>G MALY-DE 4 15627635 15627635 single base substitution G A intron_variant MALY-DE 4 15638272 15638272 single base substitution C A 3_prime_UTR_variant MALY-DE 4 15638272 15638272 single base substitution C A downstream_gene_variant MALY-DE 4 15638272 15638272 single base substitution C A exon_variant MALY-DE 4 15638272 15638272 single base substitution C A missense_variant G124V 371G>T MALY-DE 4 15638272 15638272 single base substitution C A missense_variant G164V 491G>T MALY-DE 4 15638272 15638272 single base substitution C A missense_variant G187V 560G>T MALY-DE 4 15638272 15638272 single base substitution C A missense_variant G204V 611G>T MALY-DE 4 15638272 15638272 single base substitution C A missense_variant G78V 233G>T MALY-DE 4 15653562 15653562 single base substitution T A intron_variant MALY-DE 4 15662344 15662344 single base substitution A T intron_variant MALY-DE 4 15662344 15662344 single base substitution A T upstream_gene_variant MALY-DE 4 15667073 15667073 single base substitution G T intron_variant MALY-DE 4 15667648 15667648 single base substitution A T intron_variant MALY-DE 4 15670475 15670475 single base substitution A T intron_variant MALY-DE 4 15673079 15673079 single base substitution A T intron_variant MALY-DE 4 15674304 15674304 single base substitution G A intron_variant MALY-DE 4 15688237 15688237 single base substitution G A upstream_gene_variant MELA-AU 4 15601556 15601556 single base substitution G A downstream_gene_variant MELA-AU 4 15601955 15601955 single base substitution G A downstream_gene_variant MELA-AU 4 15602248 15602248 single base substitution G A downstream_gene_variant MELA-AU 4 15602538 15602538 single base substitution A G downstream_gene_variant MELA-AU 4 15602632 15602632 single base substitution A T downstream_gene_variant MELA-AU 4 15604335 15604335 single base substitution G C downstream_gene_variant MELA-AU 4 15604872 15604872 single base substitution C A downstream_gene_variant MELA-AU 4 15604877 15604877 single base substitution T A downstream_gene_variant MELA-AU 4 15606317 15606317 single base substitution G A 3_prime_UTR_variant MELA-AU 4 15606317 15606317 single base substitution G A downstream_gene_variant MELA-AU 4 15606632 15606632 single base substitution C T 3_prime_UTR_variant MELA-AU 4 15607813 15607813 single base substitution A C intron_variant MELA-AU 4 15609561 15609561 single base substitution C A downstream_gene_variant MELA-AU 4 15609561 15609561 single base substitution C A intron_variant MELA-AU 4 15609726 15609726 single base substitution G A downstream_gene_variant MELA-AU 4 15609726 15609726 single base substitution G A intron_variant MELA-AU 4 15610035 15610035 single base substitution G A downstream_gene_variant MELA-AU 4 15610035 15610035 single base substitution G A intron_variant MELA-AU 4 15611537 15611537 single base substitution T C downstream_gene_variant MELA-AU 4 15611537 15611537 single base substitution T C intron_variant MELA-AU 4 15612893 15612893 single base substitution A C downstream_gene_variant MELA-AU 4 15612893 15612893 single base substitution A C intron_variant MELA-AU 4 15613868 15613868 single base substitution C T exon_variant MELA-AU 4 15613868 15613868 single base substitution C T intron_variant MELA-AU 4 15615071 15615071 single base substitution C T intron_variant MELA-AU 4 15615092 15615092 single base substitution C T intron_variant MELA-AU 4 15615672 15615672 single base substitution C T intron_variant MELA-AU 4 15615826 15615826 single base substitution C T intron_variant MELA-AU 4 15616144 15616144 single base substitution C T intron_variant MELA-AU 4 15616718 15616718 single base substitution G A intron_variant MELA-AU 4 15618776 15618776 single base substitution G A intron_variant MELA-AU 4 15618865 15618865 single base substitution A G intron_variant MELA-AU 4 15619627 15619627 single base substitution G A intron_variant MELA-AU 4 15620154 15620154 single base substitution A T intron_variant MELA-AU 4 15620455 15620455 single base substitution C T intron_variant MELA-AU 4 15620686 15620686 single base substitution G A intron_variant MELA-AU 4 15622894 15622894 single base substitution A G intron_variant MELA-AU 4 15624101 15624101 single base substitution A C intron_variant MELA-AU 4 15624547 15624547 single base substitution G A intron_variant MELA-AU 4 15624738 15624738 single base substitution G A intron_variant MELA-AU 4 15624912 15624912 single base substitution C T intron_variant MELA-AU 4 15625157 15625157 single base substitution G A intron_variant MELA-AU 4 15625470 15625470 single base substitution G A intron_variant MELA-AU 4 15625744 15625744 single base substitution G A intron_variant MELA-AU 4 15626415 15626415 single base substitution G A intron_variant MELA-AU 4 15626860 15626860 single base substitution G A intron_variant MELA-AU 4 15627675 15627675 single base substitution G A intron_variant MELA-AU 4 15629211 15629211 single base substitution A C intron_variant MELA-AU 4 15630395 15630395 single base substitution G C intron_variant MELA-AU 4 15630886 15630886 single base substitution G A intron_variant MELA-AU 4 15632473 15632473 single base substitution G A intron_variant MELA-AU 4 15632562 15632562 single base substitution T A intron_variant MELA-AU 4 15633539 15633539 single base substitution T C downstream_gene_variant MELA-AU 4 15633539 15633539 single base substitution T C intron_variant MELA-AU 4 15633842 15633842 single base substitution G A downstream_gene_variant MELA-AU 4 15633842 15633842 single base substitution G A intron_variant MELA-AU 4 15634296 15634296 single base substitution C T downstream_gene_variant MELA-AU 4 15634296 15634296 single base substitution C T intron_variant MELA-AU 4 15635045 15635045 single base substitution G A downstream_gene_variant MELA-AU 4 15635045 15635045 single base substitution G A intron_variant MELA-AU 4 15635404 15635405 multiple base substitution (>=2bp and <=200bp) GT AA downstream_gene_variant MELA-AU 4 15635404 15635405 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 4 15635597 15635597 single base substitution G A downstream_gene_variant MELA-AU 4 15635597 15635597 single base substitution G A intron_variant MELA-AU 4 15635646 15635646 single base substitution A T downstream_gene_variant MELA-AU 4 15635646 15635646 single base substitution A T intron_variant MELA-AU 4 15635846 15635846 single base substitution C T downstream_gene_variant MELA-AU 4 15635846 15635846 single base substitution C T intron_variant MELA-AU 4 15636684 15636684 single base substitution G A downstream_gene_variant MELA-AU 4 15636684 15636684 single base substitution G A intron_variant MELA-AU 4 15638123 15638123 single base substitution C T 3_prime_UTR_variant MELA-AU 4 15638123 15638123 single base substitution C T downstream_gene_variant MELA-AU 4 15638123 15638123 single base substitution C T exon_variant MELA-AU 4 15638123 15638123 single base substitution C T missense_variant A128T 382G>A MELA-AU 4 15638123 15638123 single base substitution C T missense_variant A174T 520G>A MELA-AU 4 15638123 15638123 single base substitution C T missense_variant A237T 709G>A MELA-AU 4 15638123 15638123 single base substitution C T missense_variant A254T 760G>A MELA-AU 4 15640139 15640139 single base substitution G A 3_prime_UTR_variant MELA-AU 4 15640139 15640139 single base substitution G A downstream_gene_variant MELA-AU 4 15640139 15640139 single base substitution G A exon_variant MELA-AU 4 15640139 15640139 single base substitution G A missense_variant S112L 335C>T MELA-AU 4 15640139 15640139 single base substitution G A missense_variant S154L 461C>T MELA-AU 4 15640139 15640139 single base substitution G A missense_variant S175L 524C>T MELA-AU 4 15640139 15640139 single base substitution G A missense_variant S192L 575C>T MELA-AU 4 15640139 15640139 single base substitution G A missense_variant S66L 197C>T MELA-AU 4 15640349 15640349 single base substitution T A downstream_gene_variant MELA-AU 4 15640349 15640349 single base substitution T A intron_variant MELA-AU 4 15641041 15641041 single base substitution C T downstream_gene_variant MELA-AU 4 15641041 15641041 single base substitution C T intron_variant MELA-AU 4 15641757 15641758 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 4 15641757 15641758 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 15642101 15642101 single base substitution G A downstream_gene_variant MELA-AU 4 15642101 15642101 single base substitution G A intron_variant MELA-AU 4 15642235 15642235 single base substitution A G downstream_gene_variant MELA-AU 4 15642235 15642235 single base substitution A G intron_variant MELA-AU 4 15643083 15643083 single base substitution A G intron_variant MELA-AU 4 15643126 15643126 single base substitution A G intron_variant MELA-AU 4 15643426 15643426 single base substitution G A intron_variant MELA-AU 4 15643558 15643559 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 15643989 15643989 single base substitution G A intron_variant MELA-AU 4 15643990 15643990 single base substitution G A intron_variant MELA-AU 4 15645007 15645007 single base substitution G A intron_variant MELA-AU 4 15645007 15645007 single base substitution G C intron_variant MELA-AU 4 15646096 15646096 single base substitution T C intron_variant MELA-AU 4 15646260 15646260 single base substitution C T 5_prime_UTR_variant MELA-AU 4 15646260 15646260 single base substitution C T exon_variant MELA-AU 4 15646260 15646260 single base substitution C T intron_variant MELA-AU 4 15646260 15646260 single base substitution C T synonymous_variant K14K 42G>A MELA-AU 4 15646260 15646260 single base substitution C T synonymous_variant K33K 99G>A MELA-AU 4 15646260 15646260 single base substitution C T synonymous_variant K35K 105G>A MELA-AU 4 15646260 15646260 single base substitution C T synonymous_variant K4K 12G>A MELA-AU 4 15646260 15646260 single base substitution C T synonymous_variant K52K 156G>A MELA-AU 4 15647275 15647275 single base substitution C G intron_variant MELA-AU 4 15647275 15647275 single base substitution C G upstream_gene_variant MELA-AU 4 15648773 15648773 single base substitution G A intron_variant MELA-AU 4 15648773 15648773 single base substitution G A upstream_gene_variant MELA-AU 4 15649664 15649664 single base substitution G A intron_variant MELA-AU 4 15649664 15649664 single base substitution G A upstream_gene_variant MELA-AU 4 15651364 15651364 single base substitution G A intron_variant MELA-AU 4 15651592 15651592 single base substitution A T intron_variant MELA-AU 4 15651691 15651691 single base substitution T A intron_variant MELA-AU 4 15652160 15652172 deletion of <=200bp TAAAGTTATATAC - intron_variant MELA-AU 4 15652809 15652809 single base substitution C T intron_variant MELA-AU 4 15654942 15654942 single base substitution A G intron_variant MELA-AU 4 15656280 15656280 single base substitution G T intron_variant MELA-AU 4 15660393 15660393 single base substitution G A downstream_gene_variant MELA-AU 4 15660393 15660393 single base substitution G A intron_variant MELA-AU 4 15660393 15660393 single base substitution G A upstream_gene_variant MELA-AU 4 15660772 15660772 single base substitution A T downstream_gene_variant MELA-AU 4 15660772 15660772 single base substitution A T intron_variant MELA-AU 4 15660772 15660772 single base substitution A T upstream_gene_variant MELA-AU 4 15661796 15661796 single base substitution G A intron_variant MELA-AU 4 15661796 15661796 single base substitution G A upstream_gene_variant MELA-AU 4 15662475 15662475 single base substitution G A intron_variant MELA-AU 4 15662475 15662475 single base substitution G A upstream_gene_variant MELA-AU 4 15665162 15665162 single base substitution G A intron_variant MELA-AU 4 15665162 15665162 single base substitution G A upstream_gene_variant MELA-AU 4 15665546 15665546 single base substitution A G intron_variant MELA-AU 4 15665546 15665546 single base substitution A G upstream_gene_variant MELA-AU 4 15665769 15665769 single base substitution G A intron_variant MELA-AU 4 15665769 15665769 single base substitution G A upstream_gene_variant MELA-AU 4 15666078 15666078 single base substitution G A intron_variant MELA-AU 4 15666078 15666078 single base substitution G A upstream_gene_variant MELA-AU 4 15666141 15666141 single base substitution A C intron_variant MELA-AU 4 15666141 15666141 single base substitution A C upstream_gene_variant MELA-AU 4 15669210 15669210 single base substitution A T intron_variant MELA-AU 4 15669218 15669218 single base substitution G T intron_variant MELA-AU 4 15669280 15669280 single base substitution A T intron_variant MELA-AU 4 15669489 15669489 single base substitution A G intron_variant MELA-AU 4 15669741 15669741 single base substitution T A intron_variant MELA-AU 4 15671056 15671056 single base substitution G A intron_variant MELA-AU 4 15672761 15672761 single base substitution G A intron_variant MELA-AU 4 15672872 15672872 single base substitution G A intron_variant MELA-AU 4 15673587 15673587 single base substitution C T intron_variant MELA-AU 4 15674047 15674047 single base substitution G A intron_variant MELA-AU 4 15674248 15674248 single base substitution G A intron_variant MELA-AU 4 15674958 15674958 single base substitution G A intron_variant MELA-AU 4 15676578 15676578 single base substitution G A intron_variant MELA-AU 4 15676776 15676776 single base substitution G A intron_variant MELA-AU 4 15677073 15677073 single base substitution C T intron_variant MELA-AU 4 15677298 15677298 single base substitution A C intron_variant MELA-AU 4 15678478 15678479 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU 4 15678676 15678676 single base substitution C T intron_variant MELA-AU 4 15678677 15678677 single base substitution G A intron_variant MELA-AU 4 15678770 15678770 single base substitution G A intron_variant MELA-AU 4 15679237 15679237 single base substitution G A intron_variant MELA-AU 4 15679496 15679496 single base substitution G A intron_variant MELA-AU 4 15679605 15679605 single base substitution G A intron_variant MELA-AU 4 15680132 15680132 single base substitution T C intron_variant MELA-AU 4 15682219 15682219 single base substitution G A intron_variant MELA-AU 4 15683142 15683143 multiple base substitution (>=2bp and <=200bp) CC TT 5_prime_UTR_variant MELA-AU 4 15683142 15683143 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 4 15683666 15683666 single base substitution G C upstream_gene_variant MELA-AU 4 15685592 15685592 single base substitution C T upstream_gene_variant MELA-AU 4 15685861 15685861 single base substitution G C upstream_gene_variant MELA-AU 4 15686232 15686232 single base substitution C T upstream_gene_variant MELA-AU 4 15687023 15687023 single base substitution C T upstream_gene_variant MELA-AU 4 15687070 15687070 single base substitution C T upstream_gene_variant MELA-AU 4 15687485 15687485 single base substitution G A upstream_gene_variant ORCA-IN 4 15601375 15601375 single base substitution C G downstream_gene_variant ORCA-IN 4 15630408 15630408 insertion of <=200bp - CACACACACG intron_variant ORCA-IN 4 15680998 15680998 single base substitution A C intron_variant ORCA-IN 4 15683307 15683307 single base substitution C A upstream_gene_variant OV-AU 4 15602257 15602257 single base substitution G T downstream_gene_variant OV-AU 4 15604135 15604135 single base substitution C A downstream_gene_variant OV-AU 4 15627490 15627490 single base substitution G T 3_prime_UTR_variant OV-AU 4 15627490 15627490 single base substitution G T exon_variant OV-AU 4 15627490 15627490 single base substitution G T missense_variant T286K 857C>A OV-AU 4 15627490 15627490 single base substitution G T missense_variant T332K 995C>A OV-AU 4 15627490 15627490 single base substitution G T missense_variant T395K 1184C>A OV-AU 4 15627490 15627490 single base substitution G T missense_variant T412K 1235C>A OV-AU 4 15628002 15628002 single base substitution T A intron_variant OV-AU 4 15631358 15631358 single base substitution C A intron_variant OV-AU 4 15645176 15645176 single base substitution C A intron_variant OV-AU 4 15651249 15651249 single base substitution A G intron_variant OV-AU 4 15651249 15651249 single base substitution A G upstream_gene_variant OV-AU 4 15658258 15658258 single base substitution G A downstream_gene_variant OV-AU 4 15658258 15658258 single base substitution G A intron_variant OV-AU 4 15658258 15658258 single base substitution G A upstream_gene_variant OV-AU 4 15658265 15658265 single base substitution G C downstream_gene_variant OV-AU 4 15658265 15658265 single base substitution G C intron_variant OV-AU 4 15658265 15658265 single base substitution G C upstream_gene_variant OV-AU 4 15658273 15658273 single base substitution G A downstream_gene_variant OV-AU 4 15658273 15658273 single base substitution G A intron_variant OV-AU 4 15658273 15658273 single base substitution G A upstream_gene_variant OV-AU 4 15658479 15658479 single base substitution G T downstream_gene_variant OV-AU 4 15658479 15658479 single base substitution G T intron_variant OV-AU 4 15658479 15658479 single base substitution G T upstream_gene_variant OV-AU 4 15658560 15658560 single base substitution G A downstream_gene_variant OV-AU 4 15658560 15658560 single base substitution G A intron_variant OV-AU 4 15658560 15658560 single base substitution G A upstream_gene_variant OV-AU 4 15658561 15658561 single base substitution A T downstream_gene_variant OV-AU 4 15658561 15658561 single base substitution A T intron_variant OV-AU 4 15658561 15658561 single base substitution A T upstream_gene_variant OV-AU 4 15670985 15670985 single base substitution T G intron_variant OV-AU 4 15671729 15671729 single base substitution G T intron_variant OV-AU 4 15674065 15674065 single base substitution C A intron_variant OV-AU 4 15674926 15674926 single base substitution T G intron_variant OV-AU 4 15684230 15684230 single base substitution C T upstream_gene_variant OV-US 4 15628522 15628531 deletion of <=200bp AGTCTGGGTA - 3_prime_UTR_variant OV-US 4 15628522 15628531 deletion of <=200bp AGTCTGGGTA - exon_variant OV-US 4 15628522 15628531 deletion of <=200bp AGTCTGGGTA - frameshift_variant LTQT237 OV-US 4 15628522 15628531 deletion of <=200bp AGTCTGGGTA - frameshift_variant LTQT283 OV-US 4 15628522 15628531 deletion of <=200bp AGTCTGGGTA - frameshift_variant LTQT346 OV-US 4 15628522 15628531 deletion of <=200bp AGTCTGGGTA - frameshift_variant LTQT363 PACA-AU 4 15606018 15606018 single base substitution T A downstream_gene_variant PACA-AU 4 15607285 15607285 single base substitution A G 3_prime_UTR_variant PACA-AU 4 15609786 15609786 single base substitution A G downstream_gene_variant PACA-AU 4 15609786 15609786 single base substitution A G intron_variant PACA-AU 4 15616992 15616992 single base substitution C G intron_variant PACA-AU 4 15623617 15623617 single base substitution G A intron_variant PACA-AU 4 15625161 15625161 single base substitution T C intron_variant PACA-AU 4 15626989 15626989 single base substitution G A 3_prime_UTR_variant PACA-AU 4 15626989 15626989 single base substitution G A exon_variant PACA-AU 4 15626989 15626989 single base substitution G A missense_variant P453L 1358C>T PACA-AU 4 15626989 15626989 single base substitution G A missense_variant P499L 1496C>T PACA-AU 4 15626989 15626989 single base substitution G A missense_variant P562L 1685C>T PACA-AU 4 15626989 15626989 single base substitution G A missense_variant P579L 1736C>T PACA-AU 4 15629472 15629472 single base substitution T G intron_variant PACA-AU 4 15639529 15639529 single base substitution A T downstream_gene_variant PACA-AU 4 15639529 15639529 single base substitution A T intron_variant PACA-AU 4 15647153 15647153 single base substitution C A intron_variant PACA-AU 4 15647153 15647153 single base substitution C A upstream_gene_variant PACA-AU 4 15648087 15648087 single base substitution A G intron_variant PACA-AU 4 15648087 15648087 single base substitution A G upstream_gene_variant PACA-AU 4 15648863 15648863 single base substitution A G intron_variant PACA-AU 4 15648863 15648863 single base substitution A G upstream_gene_variant PACA-AU 4 15650262 15650262 single base substitution T A intron_variant PACA-AU 4 15650262 15650262 single base substitution T A upstream_gene_variant PACA-AU 4 15657102 15657102 single base substitution C T downstream_gene_variant PACA-AU 4 15657102 15657102 single base substitution C T intron_variant PACA-AU 4 15657102 15657102 single base substitution C T upstream_gene_variant PACA-AU 4 15659986 15659986 single base substitution G A downstream_gene_variant PACA-AU 4 15659986 15659986 single base substitution G A intron_variant PACA-AU 4 15659986 15659986 single base substitution G A upstream_gene_variant PACA-AU 4 15683278 15683278 single base substitution A G exon_variant PACA-AU 4 15683278 15683278 single base substitution A G upstream_gene_variant PACA-AU 4 15684037 15684037 single base substitution C A upstream_gene_variant PACA-AU 4 15688200 15688200 insertion of <=200bp - A upstream_gene_variant PACA-CA 4 15601242 15601242 single base substitution C T downstream_gene_variant PACA-CA 4 15603076 15603076 single base substitution G C downstream_gene_variant PACA-CA 4 15605411 15605434 deletion of <=200bp ACTTGCTGCAGCTTCTATATTAGC - downstream_gene_variant PACA-CA 4 15606370 15606370 single base substitution A G 3_prime_UTR_variant PACA-CA 4 15606370 15606370 single base substitution A G downstream_gene_variant PACA-CA 4 15608590 15608590 single base substitution A G intron_variant PACA-CA 4 15616485 15616485 single base substitution T A intron_variant PACA-CA 4 15618823 15618823 single base substitution G T intron_variant PACA-CA 4 15620763 15620763 single base substitution G A intron_variant PACA-CA 4 15621306 15621306 single base substitution T C intron_variant PACA-CA 4 15621795 15621795 deletion of <=200bp A - intron_variant PACA-CA 4 15637058 15637058 single base substitution T A downstream_gene_variant PACA-CA 4 15637058 15637058 single base substitution T A intron_variant PACA-CA 4 15642724 15642724 single base substitution A G intron_variant PACA-CA 4 15644314 15644314 single base substitution C T intron_variant PACA-CA 4 15649047 15649047 single base substitution G C intron_variant PACA-CA 4 15649047 15649047 single base substitution G C upstream_gene_variant PACA-CA 4 15650893 15650893 single base substitution T G intron_variant PACA-CA 4 15650893 15650893 single base substitution T G upstream_gene_variant PACA-CA 4 15652928 15652928 insertion of <=200bp - A intron_variant PACA-CA 4 15656989 15656989 single base substitution C T 5_prime_UTR_variant PACA-CA 4 15656989 15656989 single base substitution C T downstream_gene_variant PACA-CA 4 15656989 15656989 single base substitution C T intron_variant PACA-CA 4 15656989 15656989 single base substitution C T upstream_gene_variant PACA-CA 4 15658992 15658992 single base substitution C A downstream_gene_variant PACA-CA 4 15658992 15658992 single base substitution C A intron_variant PACA-CA 4 15658992 15658992 single base substitution C A upstream_gene_variant PACA-CA 4 15659121 15659123 deletion of <=200bp CAA - downstream_gene_variant PACA-CA 4 15659121 15659123 deletion of <=200bp CAA - intron_variant PACA-CA 4 15659121 15659123 deletion of <=200bp CAA - upstream_gene_variant PACA-CA 4 15666355 15666355 single base substitution A T intron_variant PACA-CA 4 15666355 15666355 single base substitution A T upstream_gene_variant PACA-CA 4 15672173 15672173 single base substitution T G intron_variant PACA-CA 4 15676524 15676524 single base substitution G A intron_variant PACA-CA 4 15677879 15677879 single base substitution G A intron_variant PAEN-AU 4 15610188 15610188 single base substitution C T downstream_gene_variant PAEN-AU 4 15610188 15610188 single base substitution C T intron_variant PAEN-AU 4 15617490 15617490 single base substitution G A intron_variant PAEN-IT 4 15617684 15617684 single base substitution G A intron_variant PAEN-IT 4 15641771 15641771 single base substitution C T downstream_gene_variant PAEN-IT 4 15641771 15641771 single base substitution C T intron_variant PAEN-IT 4 15651924 15651924 single base substitution A G intron_variant PAEN-IT 4 15655332 15655332 single base substitution G A intron_variant PBCA-DE 4 15607479 15607479 single base substitution A T intron_variant PBCA-DE 4 15618150 15618150 single base substitution G C intron_variant PBCA-DE 4 15618151 15618151 single base substitution T C intron_variant PBCA-DE 4 15621486 15621486 single base substitution T A intron_variant PBCA-DE 4 15622848 15622848 insertion of <=200bp - A intron_variant PBCA-DE 4 15627878 15627889 deletion of <=200bp GTCAGCAGAAGT - intron_variant PBCA-DE 4 15637223 15637223 insertion of <=200bp - A downstream_gene_variant PBCA-DE 4 15637223 15637223 insertion of <=200bp - A intron_variant PBCA-DE 4 15639219 15639219 single base substitution A G downstream_gene_variant PBCA-DE 4 15639219 15639219 single base substitution A G intron_variant PBCA-DE 4 15644192 15644192 single base substitution C A intron_variant PBCA-DE 4 15648859 15648859 single base substitution A G intron_variant PBCA-DE 4 15648859 15648859 single base substitution A G upstream_gene_variant PBCA-DE 4 15687335 15687335 single base substitution A G upstream_gene_variant PRAD-CA 4 15677206 15677206 single base substitution T C intron_variant PRAD-CA 4 15677208 15677208 single base substitution T C intron_variant PRAD-UK 4 15606630 15606630 single base substitution T C 3_prime_UTR_variant PRAD-UK 4 15606630 15606630 single base substitution T C downstream_gene_variant PRAD-UK 4 15607425 15607425 single base substitution G A intron_variant PRAD-UK 4 15622065 15622065 single base substitution G C intron_variant PRAD-UK 4 15627071 15627071 deletion of <=200bp A - 3_prime_UTR_variant PRAD-UK 4 15627071 15627071 deletion of <=200bp A - exon_variant PRAD-UK 4 15627071 15627071 deletion of <=200bp A - frameshift_variant C426 PRAD-UK 4 15627071 15627071 deletion of <=200bp A - frameshift_variant C472 PRAD-UK 4 15627071 15627071 deletion of <=200bp A - frameshift_variant C535 PRAD-UK 4 15627071 15627071 deletion of <=200bp A - frameshift_variant C552 PRAD-UK 4 15629090 15629090 single base substitution G C intron_variant PRAD-UK 4 15639240 15639240 insertion of <=200bp - TTTA downstream_gene_variant PRAD-UK 4 15639240 15639240 insertion of <=200bp - TTTA intron_variant PRAD-UK 4 15642522 15642522 single base substitution A T intron_variant PRAD-UK 4 15645465 15645465 single base substitution A T intron_variant PRAD-UK 4 15657289 15657289 single base substitution T A downstream_gene_variant PRAD-UK 4 15657289 15657289 single base substitution T A intron_variant PRAD-UK 4 15657289 15657289 single base substitution T A upstream_gene_variant PRAD-UK 4 15658699 15658699 single base substitution C G downstream_gene_variant PRAD-UK 4 15658699 15658699 single base substitution C G intron_variant PRAD-UK 4 15658699 15658699 single base substitution C G upstream_gene_variant PRAD-UK 4 15659476 15659476 single base substitution C G downstream_gene_variant PRAD-UK 4 15659476 15659476 single base substitution C G intron_variant PRAD-UK 4 15659476 15659476 single base substitution C G upstream_gene_variant PRAD-UK 4 15659696 15659696 single base substitution C A downstream_gene_variant PRAD-UK 4 15659696 15659696 single base substitution C A intron_variant PRAD-UK 4 15659696 15659696 single base substitution C A upstream_gene_variant PRAD-UK 4 15660510 15660510 insertion of <=200bp - T downstream_gene_variant PRAD-UK 4 15660510 15660510 insertion of <=200bp - T intron_variant PRAD-UK 4 15660510 15660510 insertion of <=200bp - T upstream_gene_variant PRAD-UK 4 15674529 15674529 single base substitution A G intron_variant PRAD-UK 4 15679528 15679528 single base substitution A G intron_variant PRAD-UK 4 15682750 15682750 single base substitution T G intron_variant PRAD-UK 4 15686302 15686302 single base substitution A G upstream_gene_variant READ-US 4 15629605 15629605 single base substitution C T 3_prime_UTR_variant READ-US 4 15629605 15629605 single base substitution C T exon_variant READ-US 4 15629605 15629605 single base substitution C T missense_variant R189H 566G>A READ-US 4 15629605 15629605 single base substitution C T missense_variant R235H 704G>A READ-US 4 15629605 15629605 single base substitution C T missense_variant R298H 893G>A READ-US 4 15629605 15629605 single base substitution C T missense_variant R315H 944G>A RECA-EU 4 15608730 15608730 single base substitution C T downstream_gene_variant RECA-EU 4 15608730 15608730 single base substitution C T intron_variant RECA-EU 4 15609198 15609198 single base substitution C A downstream_gene_variant RECA-EU 4 15609198 15609198 single base substitution C A intron_variant RECA-EU 4 15612681 15612681 single base substitution C T downstream_gene_variant RECA-EU 4 15612681 15612681 single base substitution C T intron_variant RECA-EU 4 15624405 15624405 single base substitution C A intron_variant RECA-EU 4 15636585 15636585 single base substitution A C downstream_gene_variant RECA-EU 4 15636585 15636585 single base substitution A C intron_variant RECA-EU 4 15636586 15636586 single base substitution T A downstream_gene_variant RECA-EU 4 15636586 15636586 single base substitution T A intron_variant RECA-EU 4 15640290 15640290 single base substitution A G 3_prime_UTR_variant RECA-EU 4 15640290 15640290 single base substitution A G downstream_gene_variant RECA-EU 4 15640290 15640290 single base substitution A G exon_variant RECA-EU 4 15640290 15640290 single base substitution A G missense_variant F104L 310T>C RECA-EU 4 15640290 15640290 single base substitution A G missense_variant F125L 373T>C RECA-EU 4 15640290 15640290 single base substitution A G missense_variant F142L 424T>C RECA-EU 4 15640290 15640290 single base substitution A G missense_variant F16L 46T>C RECA-EU 4 15640290 15640290 single base substitution A G missense_variant F62L 184T>C RECA-EU 4 15640290 15640290 single base substitution A G missense_variant F87L 259T>C RECA-EU 4 15648438 15648438 single base substitution C T intron_variant RECA-EU 4 15648438 15648438 single base substitution C T upstream_gene_variant RECA-EU 4 15655552 15655552 single base substitution C T intron_variant RECA-EU 4 15661814 15661814 single base substitution T G intron_variant RECA-EU 4 15661814 15661814 single base substitution T G upstream_gene_variant RECA-EU 4 15668502 15668502 single base substitution A T intron_variant RECA-EU 4 15684666 15684666 single base substitution A C upstream_gene_variant RECA-EU 4 15687457 15687457 single base substitution T A upstream_gene_variant RECA-EU 4 15687702 15687702 single base substitution A C upstream_gene_variant SKCA-BR 4 15603014 15603014 single base substitution G A downstream_gene_variant SKCA-BR 4 15603020 15603020 single base substitution A C downstream_gene_variant SKCA-BR 4 15606496 15606496 insertion of <=200bp - AT 3_prime_UTR_variant SKCA-BR 4 15606496 15606496 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 4 15618006 15618006 insertion of <=200bp - TCACTCCTGCCATG intron_variant SKCA-BR 4 15621126 15621126 single base substitution C T intron_variant SKCA-BR 4 15629930 15629930 single base substitution G A intron_variant SKCA-BR 4 15630395 15630395 insertion of <=200bp - GACACAC intron_variant SKCA-BR 4 15633726 15633726 single base substitution G A downstream_gene_variant SKCA-BR 4 15633726 15633726 single base substitution G A intron_variant SKCA-BR 4 15634155 15634155 single base substitution C T downstream_gene_variant SKCA-BR 4 15634155 15634155 single base substitution C T intron_variant SKCA-BR 4 15640526 15640526 single base substitution A G downstream_gene_variant SKCA-BR 4 15640526 15640526 single base substitution A G intron_variant SKCA-BR 4 15641046 15641046 single base substitution G A downstream_gene_variant SKCA-BR 4 15641046 15641046 single base substitution G A intron_variant SKCA-BR 4 15642065 15642065 single base substitution C A downstream_gene_variant SKCA-BR 4 15642065 15642065 single base substitution C A intron_variant SKCA-BR 4 15646041 15646041 single base substitution G A intron_variant SKCA-BR 4 15647217 15647217 single base substitution A T intron_variant SKCA-BR 4 15647217 15647217 single base substitution A T upstream_gene_variant SKCA-BR 4 15651234 15651234 single base substitution G A intron_variant SKCA-BR 4 15651234 15651234 single base substitution G A upstream_gene_variant SKCA-BR 4 15651440 15651440 single base substitution G A intron_variant SKCA-BR 4 15653887 15653887 single base substitution C T intron_variant SKCA-BR 4 15657053 15657053 single base substitution A G downstream_gene_variant SKCA-BR 4 15657053 15657053 single base substitution A G intron_variant SKCA-BR 4 15657053 15657053 single base substitution A G upstream_gene_variant SKCA-BR 4 15660967 15660967 single base substitution C T downstream_gene_variant SKCA-BR 4 15660967 15660967 single base substitution C T intron_variant SKCA-BR 4 15660967 15660967 single base substitution C T upstream_gene_variant SKCA-BR 4 15663656 15663656 single base substitution G A intron_variant SKCA-BR 4 15663656 15663656 single base substitution G A upstream_gene_variant SKCA-BR 4 15663917 15663917 single base substitution G A intron_variant SKCA-BR 4 15663917 15663917 single base substitution G A upstream_gene_variant SKCA-BR 4 15670053 15670053 single base substitution G A intron_variant SKCA-BR 4 15672333 15672334 deletion of <=200bp GA - intron_variant SKCA-BR 4 15676346 15676346 single base substitution C T intron_variant SKCA-BR 4 15676657 15676657 single base substitution G A intron_variant SKCA-BR 4 15677109 15677109 single base substitution T C intron_variant SKCA-BR 4 15681200 15681201 deletion of <=200bp AC - intron_variant SKCA-BR 4 15684850 15684850 single base substitution C T upstream_gene_variant SKCM-US 4 15607372 15607372 single base substitution G A 3_prime_UTR_variant SKCM-US 4 15607372 15607372 single base substitution G A stop_gained R558* 1672C>T SKCM-US 4 15607372 15607372 single base substitution G A stop_gained R604* 1810C>T SKCM-US 4 15607372 15607372 single base substitution G A stop_gained R667* 1999C>T SKCM-US 4 15607372 15607372 single base substitution G A stop_gained R684* 2050C>T SKCM-US 4 15627133 15627133 single base substitution C A 3_prime_UTR_variant SKCM-US 4 15627133 15627133 single base substitution C A exon_variant SKCM-US 4 15627133 15627133 single base substitution C A missense_variant S405I 1214G>T SKCM-US 4 15627133 15627133 single base substitution C A missense_variant S451I 1352G>T SKCM-US 4 15627133 15627133 single base substitution C A missense_variant S514I 1541G>T SKCM-US 4 15627133 15627133 single base substitution C A missense_variant S531I 1592G>T SKCM-US 4 15627231 15627231 single base substitution A C 3_prime_UTR_variant SKCM-US 4 15627231 15627231 single base substitution A C exon_variant SKCM-US 4 15627231 15627231 single base substitution A C missense_variant H372Q 1116T>G SKCM-US 4 15627231 15627231 single base substitution A C missense_variant H418Q 1254T>G SKCM-US 4 15627231 15627231 single base substitution A C missense_variant H481Q 1443T>G SKCM-US 4 15627231 15627231 single base substitution A C missense_variant H498Q 1494T>G SKCM-US 4 15640311 15640311 single base substitution G A 3_prime_UTR_variant SKCM-US 4 15640311 15640311 single base substitution G A downstream_gene_variant SKCM-US 4 15640311 15640311 single base substitution G A exon_variant SKCM-US 4 15640311 15640311 single base substitution G A stop_gained Q118* 352C>T SKCM-US 4 15640311 15640311 single base substitution G A stop_gained Q135* 403C>T SKCM-US 4 15640311 15640311 single base substitution G A stop_gained Q55* 163C>T SKCM-US 4 15640311 15640311 single base substitution G A stop_gained Q80* 238C>T SKCM-US 4 15640311 15640311 single base substitution G A stop_gained Q9* 25C>T SKCM-US 4 15640311 15640311 single base substitution G A stop_gained Q97* 289C>T STAD-US 4 15601172 15601172 deletion of <=200bp A - downstream_gene_variant STAD-US 4 15601259 15601259 insertion of <=200bp - A downstream_gene_variant STAD-US 4 15607351 15607351 single base substitution C T 3_prime_UTR_variant STAD-US 4 15607351 15607351 single base substitution C T missense_variant E565K 1693G>A STAD-US 4 15607351 15607351 single base substitution C T missense_variant E611K 1831G>A STAD-US 4 15607351 15607351 single base substitution C T missense_variant E674K 2020G>A STAD-US 4 15607351 15607351 single base substitution C T missense_variant E691K 2071G>A STAD-US 4 15614035 15614035 single base substitution A C missense_variant V492G 1475T>G STAD-US 4 15614035 15614035 single base substitution A C missense_variant V538G 1613T>G STAD-US 4 15614035 15614035 single base substitution A C missense_variant V601G 1802T>G STAD-US 4 15614035 15614035 single base substitution A C missense_variant V618G 1853T>G STAD-US 4 15614035 15614035 single base substitution A C splice_region_variant STAD-US 4 15627020 15627020 single base substitution T G 3_prime_UTR_variant STAD-US 4 15627020 15627020 single base substitution T G exon_variant STAD-US 4 15627020 15627020 single base substitution T G missense_variant M443L 1327A>C STAD-US 4 15627020 15627020 single base substitution T G missense_variant M489L 1465A>C STAD-US 4 15627020 15627020 single base substitution T G missense_variant M552L 1654A>C STAD-US 4 15627020 15627020 single base substitution T G missense_variant M569L 1705A>C STAD-US 4 15628520 15628520 single base substitution T A 3_prime_UTR_variant STAD-US 4 15628520 15628520 single base substitution T A exon_variant STAD-US 4 15628520 15628520 single base substitution T A missense_variant D241V 722A>T STAD-US 4 15628520 15628520 single base substitution T A missense_variant D287V 860A>T STAD-US 4 15628520 15628520 single base substitution T A missense_variant D350V 1049A>T STAD-US 4 15628520 15628520 single base substitution T A missense_variant D367V 1100A>T STAD-US 4 15642491 15642491 single base substitution A G 3_prime_UTR_variant STAD-US 4 15642491 15642491 single base substitution A G 5_prime_UTR_variant STAD-US 4 15642491 15642491 single base substitution A G exon_variant STAD-US 4 15642491 15642491 single base substitution A G intron_variant STAD-US 4 15642491 15642491 single base substitution A G synonymous_variant L106L 316T>C STAD-US 4 15642491 15642491 single base substitution A G synonymous_variant L51L 151T>C STAD-US 4 15642491 15642491 single base substitution A G synonymous_variant L68L 202T>C STAD-US 4 15642491 15642491 single base substitution A G synonymous_variant L87L 259T>C STAD-US 4 15642491 15642491 single base substitution A G synonymous_variant L89L 265T>C THCA-SA 4 15640168 15640168 single base substitution C T 3_prime_UTR_variant THCA-SA 4 15640168 15640168 single base substitution C T downstream_gene_variant THCA-SA 4 15640168 15640168 single base substitution C T exon_variant THCA-SA 4 15640168 15640168 single base substitution C T synonymous_variant K102K 306G>A THCA-SA 4 15640168 15640168 single base substitution C T synonymous_variant K127K 381G>A THCA-SA 4 15640168 15640168 single base substitution C T synonymous_variant K144K 432G>A THCA-SA 4 15640168 15640168 single base substitution C T synonymous_variant K165K 495G>A THCA-SA 4 15640168 15640168 single base substitution C T synonymous_variant K182K 546G>A THCA-SA 4 15640168 15640168 single base substitution C T synonymous_variant K56K 168G>A THCA-US 4 15629584 15629584 single base substitution T C 3_prime_UTR_variant THCA-US 4 15629584 15629584 single base substitution T C exon_variant THCA-US 4 15629584 15629584 single base substitution T C missense_variant H196R 587A>G THCA-US 4 15629584 15629584 single base substitution T C missense_variant H242R 725A>G THCA-US 4 15629584 15629584 single base substitution T C missense_variant H305R 914A>G THCA-US 4 15629584 15629584 single base substitution T C missense_variant H322R 965A>G UCEC-US 4 15601207 15601207 single base substitution C T downstream_gene_variant UCEC-US 4 15607391 15607391 single base substitution C A 3_prime_UTR_variant UCEC-US 4 15607391 15607391 single base substitution C A missense_variant Q551H 1653G>T UCEC-US 4 15607391 15607391 single base substitution C A missense_variant Q597H 1791G>T UCEC-US 4 15607391 15607391 single base substitution C A missense_variant Q660H 1980G>T UCEC-US 4 15607391 15607391 single base substitution C A missense_variant Q677H 2031G>T UCEC-US 4 15613888 15613888 single base substitution C T exon_variant UCEC-US 4 15613888 15613888 single base substitution C T splice_donor_variant UCEC-US 4 15614001 15614001 single base substitution C A 3_prime_UTR_variant UCEC-US 4 15614001 15614001 single base substitution C A exon_variant UCEC-US 4 15614001 15614001 single base substitution C A missense_variant E503D 1509G>T UCEC-US 4 15614001 15614001 single base substitution C A missense_variant E549D 1647G>T UCEC-US 4 15614001 15614001 single base substitution C A missense_variant E612D 1836G>T UCEC-US 4 15614001 15614001 single base substitution C A missense_variant E629D 1887G>T UCEC-US 4 15626978 15626978 single base substitution C A 3_prime_UTR_variant UCEC-US 4 15626978 15626978 single base substitution C A exon_variant UCEC-US 4 15626978 15626978 single base substitution C A missense_variant D457Y 1369G>T UCEC-US 4 15626978 15626978 single base substitution C A missense_variant D503Y 1507G>T UCEC-US 4 15626978 15626978 single base substitution C A missense_variant D566Y 1696G>T UCEC-US 4 15626978 15626978 single base substitution C A missense_variant D583Y 1747G>T UCEC-US 4 15626993 15626993 single base substitution A G 3_prime_UTR_variant UCEC-US 4 15626993 15626993 single base substitution A G exon_variant UCEC-US 4 15626993 15626993 single base substitution A G synonymous_variant L452L 1354T>C UCEC-US 4 15626993 15626993 single base substitution A G synonymous_variant L498L 1492T>C UCEC-US 4 15626993 15626993 single base substitution A G synonymous_variant L561L 1681T>C UCEC-US 4 15626993 15626993 single base substitution A G synonymous_variant L578L 1732T>C UCEC-US 4 15627095 15627095 single base substitution C T 3_prime_UTR_variant UCEC-US 4 15627095 15627095 single base substitution C T exon_variant UCEC-US 4 15627095 15627095 single base substitution C T missense_variant A418T 1252G>A UCEC-US 4 15627095 15627095 single base substitution C T missense_variant A464T 1390G>A UCEC-US 4 15627095 15627095 single base substitution C T missense_variant A527T 1579G>A UCEC-US 4 15627095 15627095 single base substitution C T missense_variant A544T 1630G>A UCEC-US 4 15627233 15627233 single base substitution G A 3_prime_UTR_variant UCEC-US 4 15627233 15627233 single base substitution G A exon_variant UCEC-US 4 15627233 15627233 single base substitution G A missense_variant H372Y 1114C>T UCEC-US 4 15627233 15627233 single base substitution G A missense_variant H418Y 1252C>T UCEC-US 4 15627233 15627233 single base substitution G A missense_variant H481Y 1441C>T UCEC-US 4 15627233 15627233 single base substitution G A missense_variant H498Y 1492C>T UCEC-US 4 15627271 15627271 single base substitution T G 3_prime_UTR_variant UCEC-US 4 15627271 15627271 single base substitution T G exon_variant UCEC-US 4 15627271 15627271 single base substitution T G missense_variant E359A 1076A>C UCEC-US 4 15627271 15627271 single base substitution T G missense_variant E405A 1214A>C UCEC-US 4 15627271 15627271 single base substitution T G missense_variant E468A 1403A>C UCEC-US 4 15627271 15627271 single base substitution T G missense_variant E485A 1454A>C UCEC-US 4 15627285 15627285 single base substitution C T 3_prime_UTR_variant UCEC-US 4 15627285 15627285 single base substitution C T exon_variant UCEC-US 4 15627285 15627285 single base substitution C T stop_gained W354* 1062G>A UCEC-US 4 15627285 15627285 single base substitution C T stop_gained W400* 1200G>A UCEC-US 4 15627285 15627285 single base substitution C T stop_gained W463* 1389G>A UCEC-US 4 15627285 15627285 single base substitution C T stop_gained W480* 1440G>A UCEC-US 4 15627353 15627353 single base substitution C A 3_prime_UTR_variant UCEC-US 4 15627353 15627353 single base substitution C A exon_variant UCEC-US 4 15627353 15627353 single base substitution C A stop_gained E332* 994G>T UCEC-US 4 15627353 15627353 single base substitution C A stop_gained E378* 1132G>T UCEC-US 4 15627353 15627353 single base substitution C A stop_gained E441* 1321G>T UCEC-US 4 15627353 15627353 single base substitution C A stop_gained E458* 1372G>T UCEC-US 4 15627499 15627499 single base substitution C A 3_prime_UTR_variant UCEC-US 4 15627499 15627499 single base substitution C A exon_variant UCEC-US 4 15627499 15627499 single base substitution C A missense_variant G283V 848G>T UCEC-US 4 15627499 15627499 single base substitution C A missense_variant G329V 986G>T UCEC-US 4 15627499 15627499 single base substitution C A missense_variant G392V 1175G>T UCEC-US 4 15627499 15627499 single base substitution C A missense_variant G409V 1226G>T UCEC-US 4 15627543 15627543 single base substitution C T 3_prime_UTR_variant UCEC-US 4 15627543 15627543 single base substitution C T exon_variant UCEC-US 4 15627543 15627543 single base substitution C T synonymous_variant E268E 804G>A UCEC-US 4 15627543 15627543 single base substitution C T synonymous_variant E314E 942G>A UCEC-US 4 15627543 15627543 single base substitution C T synonymous_variant E377E 1131G>A UCEC-US 4 15627543 15627543 single base substitution C T synonymous_variant E394E 1182G>A UCEC-US 4 15640237 15640237 single base substitution G A 3_prime_UTR_variant UCEC-US 4 15640237 15640237 single base substitution G A downstream_gene_variant UCEC-US 4 15640237 15640237 single base substitution G A exon_variant UCEC-US 4 15640237 15640237 single base substitution G A synonymous_variant C104C 312C>T UCEC-US 4 15640237 15640237 single base substitution G A synonymous_variant C121C 363C>T UCEC-US 4 15640237 15640237 single base substitution G A synonymous_variant C142C 426C>T UCEC-US 4 15640237 15640237 single base substitution G A synonymous_variant C159C 477C>T UCEC-US 4 15640237 15640237 single base substitution G A synonymous_variant C33C 99C>T UCEC-US 4 15640237 15640237 single base substitution G A synonymous_variant C79C 237C>T UCEC-US 4 15646301 15646301 single base substitution C T 5_prime_UTR_variant UCEC-US 4 15646301 15646301 single base substitution C T exon_variant UCEC-US 4 15646301 15646301 single base substitution C T intron_variant UCEC-US 4 15646301 15646301 single base substitution C T missense_variant D1N 1G>A UCEC-US 4 15646301 15646301 single base substitution C T missense_variant D20N 58G>A UCEC-US 4 15646301 15646301 single base substitution C T missense_variant D39N 115G>A UCEC-US 4 15646301 15646301 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PTC-14C COSM4158882 c.334C>A p.L112M Substitution - Missense 4:15640850-15640850 - 2492701 COSM5599540 c.1764G>T p.G588G Substitution - coding silent 4:15625338-15625338 - KPOPBR-20-T COSM5963396 c.1106C>T p.S369L Substitution - Missense 4:15626891-15626891 - TCGA-AP-A059-01 COSM1052491 c.1454A>C p.E485A Substitution - Missense 4:15625648-15625648 - TCGA-AN-A046-01 COSM3825446 c.365A>C p.D122A Substitution - Missense 4:15640819-15640819 - HCC86T COSM1618526 c.1683A>G p.S561S Substitution - coding silent 4:15625419-15625419 - 587224 COSM1206783 c.971T>G p.V324G Substitution - Missense 4:15627955-15627955 - ICGC_0065 COSM218792 c.1736C>T p.P579L Substitution - Missense 4:15625366-15625366 - TCGA-AX-A064-01 COSM1052489 c.1630G>A p.A544T Substitution - Missense 4:15625472-15625472 - UM-SCC-2 COSM3129536 c.1679T>C p.M560T Substitution - Missense 4:15625423-15625423 - PGBM09PT COSM1580358 c.397-3T>G p.? Unknown 4:15638697-15638697 - TCGA-FD-A3N5-01 COSM1309839 c.1737T>G p.P579P Substitution - coding silent 4:15625365-15625365 - 1N28-VS-1T28 COSM4973809 c.1828C>G p.Q610E Substitution - Missense 4:15625274-15625274 - TCGA-AP-A059-01 COSM1052512 c.477C>T p.C159C Substitution - coding silent 4:15638614-15638614 - TCGA-FS-A1ZM-06 COSM3601250 c.1592G>T p.S531I Substitution - Missense 4:15625510-15625510 - TCGA-D1-A16R-01 COSM1052511 c.516C>A p.S172R Substitution - Missense 4:15638575-15638575 - S02293 COSM5688532 c.919A>G p.I307V Substitution - Missense 4:15628007-15628007 - AOCS-092-1-6 COSM4138086 c.1235C>A p.T412K Substitution - Missense 4:15625867-15625867 - CHC121T COSM3669259 c.1116A>T p.A372A Substitution - coding silent 4:15626881-15626881 - PDA_060 COSM5001141 c.349delG p.E117fs*11 Deletion - Frameshift 4:15640835-15640835 - Multi_liver_13 COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - S02347 COSM5694286 c.1850G>A p.R617K Substitution - Missense 4:15625252-15625252 - TCGA-60-2724-01 COSM732272 c.1301A>G p.K434R Substitution - Missense 4:15625801-15625801 - TCGA-E2-A1IN-01 COSM1485792 c.651C>T p.F217F Substitution - coding silent 4:15636609-15636609 - TCGA-06-0649-01 COSM2151442 c.842A>C p.E281A Substitution - Missense 4:15630716-15630716 - LUAD-S01356 COSM398250 c.970G>C p.V324L Substitution - Missense 4:15627956-15627956 - 386 COSM4427178 c.1494_1495delTA p.H498fs*4 Deletion - Frameshift 4:15625607-15625608 - AOCS-092-3-3 COSM4138086 c.1235C>A p.T412K Substitution - Missense 4:15625867-15625867 - 37M COSM5583502 c.1140T>C p.G380G Substitution - coding silent 4:15625962-15625962 - TCGA-MK-A4N7-01 COSM3373413 c.965A>G p.H322R Substitution - Missense 4:15627961-15627961 - TCGA-AX-A0J1-01 COSM1052490 c.1492C>T p.H498Y Substitution - Missense 4:15625610-15625610 - BRC35 COSM5026125 c.584-1G>A p.? Unknown 4:15636677-15636677 - TCGA-D8-A1J8-01 COSM3825443 c.1946C>G p.S649* Substitution - Nonsense 4:15612319-15612319 - TCGA-AZ-4313-01 COSM5138793 c.122G>A p.R41H Substitution - Missense 4:15644671-15644671 - I2L-P23-Tumor-Organoid COSM5356028 c.723G>A p.T241T Substitution - coding silent 4:15636537-15636537 - TCGA-06-0649 COSM2151442 c.842A>C p.E281A Substitution - Missense 4:15630716-15630716 - SNU-C4 COSM4653780 c.1792C>T p.R598C Substitution - Missense 4:15625310-15625310 - TCGA-AA-3977-01 COSM5119309 c.397-10T>C p.? Unknown 4:15638704-15638704 - 19 COSM5746259 c.830delA p.N277fs*44 Deletion - Frameshift 4:15630728-15630728 - CHC884T COSM4958350 c.1915A>G p.I639V Substitution - Missense 4:15612350-15612350 - TCGA-D1-A103-01 COSM1052487 c.1747G>T p.D583Y Substitution - Missense 4:15625355-15625355 - TCGA-AA-A00N-01 COSM275141 c.729G>A p.S243S Substitution - coding silent 4:15636531-15636531 - CHC884T COSM4958350 c.1915A>G p.I639V Substitution - Missense 4:15612350-15612350 - Left_iliac_crest COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - P04-1243 COSM242524 c.1855T>G p.L619V Substitution - Missense 4:15612410-15612410 - TCGA-B5-A0JY-01 COSM1052493 c.1372G>T p.E458* Substitution - Nonsense 4:15625730-15625730 - ATL021 COSM5709123 c.1865G>T p.G622V Substitution - Missense 4:15612400-15612400 - TCGA-AZ-4614-01 COSM5139501 c.1124+1G>C p.? Unknown 4:15626872-15626872 - 2492702 COSM5599540 c.1764G>T p.G588G Substitution - coding silent 4:15625338-15625338 - TCGA-D1-A17Q-01 COSM1052472 c.2031G>T p.Q677H Substitution - Missense 4:15605768-15605768 - QC2-32-T2 COSM5653993 c.1652G>A p.C551Y Substitution - Missense 4:15625450-15625450 - TCGA-CC-A3MA-01 COSM4942821 c.934A>G p.M312V Substitution - Missense 4:15627992-15627992 - Left_clavicle_LN COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - T33 COSM5344655 c.396+1G>T p.? Unknown 4:15640787-15640787 - TCGA-EE-A181-06 COSM3601255 c.403C>T p.Q135* Substitution - Nonsense 4:15638688-15638688 - I2L-P23-Tumor-Biopsy COSM5356028 c.723G>A p.T241T Substitution - coding silent 4:15636537-15636537 - TCGA-BR-8680-01 COSM4123004 c.1705A>C p.M569L Substitution - Missense 4:15625397-15625397 - Single_liver_2 COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - TCGA-DM-A0XF-01 COSM1427544 c.658C>G p.L220V Substitution - Missense 4:15636602-15636602 - TCGA-B5-A11E-01 COSM1052497 c.1226G>T p.G409V Substitution - Missense 4:15625876-15625876 - TCGA-G4-6304-01 COSM5175350 c.402delT p.Q135fs*4 Deletion - Frameshift 4:15638689-15638689 - SC_9047 COSM5562717 c.15T>C p.P5P Substitution - coding silent 4:15655273-15655273 - RK084_C01 COSM1633509 c.1041+9A>G p.? Unknown 4:15627876-15627876 - TCGA-AX-A0J1-01 COSM1052482 c.1999+1G>A p.? Unknown 4:15612265-15612265 - Right_rib COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - TCGA-24-1842-01 COSM1328658 c.1134G>A p.W378* Substitution - Nonsense 4:15625968-15625968 - S01563 COSM311125 c.1124+1G>T p.? Unknown 4:15626872-15626872 - TCGA-B5-A11E-01 COSM1052488 c.1732T>C p.L578L Substitution - coding silent 4:15625370-15625370 - TCGA-13-1498-01 COSM111381 c.1089_1098del10 p.Q365fs*34 Deletion - Frameshift 4:15626899-15626908 - YUGEMA COSM5400687 c.257C>T p.S86F Substitution - Missense 4:15644536-15644536 - HCC86 COSM1618526 c.1683A>G p.S561S Substitution - coding silent 4:15625419-15625419 - TCGA-BR-6452-01 COSM4123003 c.1853T>G p.V618G Substitution - Missense 4:15612412-15612412 - tumor_4116738 COSM1161481 c.1451C>G p.A484G Substitution - Missense 4:15625651-15625651 - TCGA-C8-A133-01 COSM447537 c.1430C>A p.P477H Substitution - Missense 4:15625672-15625672 - TCGA-BR-8372-01 COSM4123010 c.316T>C p.L106L Substitution - coding silent 4:15640868-15640868 - Single_liver_4 COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - 2492700 COSM5599540 c.1764G>T p.G588G Substitution - coding silent 4:15625338-15625338 - TCGA-AP-A0LM-01 COSM1052513 c.115G>A p.D39N Substitution - Missense 4:15644678-15644678 - CSCC-10-T COSM4564453 c.1200_1201CC>TA p.L401I Substitution - Missense 4:15625901-15625902 - TCGA-HU-A4GT-01 COSM4123007 c.1100A>T p.D367V Substitution - Missense 4:15626897-15626897 - PTC-14C COSM4158881 c.338A>C p.K113T Substitution - Missense 4:15640846-15640846 - TCGA-BF-A1PZ-01 COSM4399193 c.1494T>G p.H498Q Substitution - Missense 4:15625608-15625608 - 2492703 COSM5599540 c.1764G>T p.G588G Substitution - coding silent 4:15625338-15625338 - TCGA-AA-3833-01 COSM5112527 c.899C>A p.S300Y Substitution - Missense 4:15628027-15628027 - H322T COSM1194813 c.1289C>T p.A430V Substitution - Missense 4:15625813-15625813 - TCGA-EX-A1H6-01 COSM4848891 c.2066C>G p.S689C Substitution - Missense 4:15605733-15605733 - HCC109T COSM5816747 c.1987G>T p.D663Y Substitution - Missense 4:15612278-15612278 - tumor_4188900 COSM3357786 c.611G>T p.G204V Substitution - Missense 4:15636649-15636649 - LS411 COSM4614534 c.620_621insA p.H207fs*5 Insertion - Frameshift 4:15636639-15636640 - TCGA-CK-4951-01 COSM5151797 c.1166A>T p.D389V Substitution - Missense 4:15625936-15625936 - TCGA-AA-3715-01 COSM269155 c.1157G>A p.R386Q Substitution - Missense 4:15625945-15625945 - TCGA-C8-A274-01 COSM1485793 c.481C>G p.Q161E Substitution - Missense 4:15638610-15638610 - ESCC_BICR_053T COSM5442164 c.1372G>A p.E458K Substitution - Missense 4:15625730-15625730 - TCGA-27-2528-01 COSM3409124 c.1790G>T p.G597V Substitution - Missense 4:15625312-15625312 - TCGA-AP-A051-01 COSM1052483 c.1887G>T p.E629D Substitution - Missense 4:15612378-15612378 - TCGA-EE-A2GC-06 COSM3917308 c.2050C>T p.R684* Substitution - Nonsense 4:15605749-15605749 - TCGA-CA-6717-01 COSM1427545 c.417G>T p.M139I Substitution - Missense 4:15638674-15638674 - TCGA-AX-A05Z-01 COSM1052492 c.1440G>A p.W480* Substitution - Nonsense 4:15625662-15625662 - TCGA-AD-A5EJ-01 COSM3129615 c.552T>A p.F184L Substitution - Missense 4:15638539-15638539 - H226 COSM1196709 c.1519A>G p.M507V Substitution - Missense 4:15625583-15625583 - Left_adrenal COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - S01563 COSM311125 c.1124+1G>T p.? Unknown 4:15626872-15626872 - Au2 COSM5599540 c.1764G>T p.G588G Substitution - coding silent 4:15625338-15625338 - LIM2405 COSM4613621 c.1256delT p.L419fs*1 Deletion - Frameshift 4:15625846-15625846 - 8031644 COSM218792 c.1736C>T p.P579L Substitution - Missense 4:15625366-15625366 - VACO10 COSM4656977 c.444G>A p.K148K Substitution - coding silent 4:15638647-15638647 - TCGA-Q1-A73S-01 COSM4836671 c.2017G>T p.A673S Substitution - Missense 4:15605782-15605782 - ESO-539 COSM1252244 c.1999G>A p.G667S Substitution - Missense 4:15612266-15612266 - TCGA-E9-A1RD-01 COSM1485791 c.911C>T p.S304L Substitution - Missense 4:15628015-15628015 - 587316 COSM1206784 c.53T>C p.M18T Substitution - Missense 4:15655235-15655235 - TCGA-F1-6177-01 COSM4122995 c.2071G>A p.E691K Substitution - Missense 4:15605728-15605728 - 0114_CRUK_PC_0114_T1_DNA COSM5422433 c.2000-3C>T p.? Unknown 4:15605802-15605802 - NCI-H226 COSM1196709 c.1519A>G p.M507V Substitution - Missense 4:15625583-15625583 - Left_rib COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - ESOSCC162T COSM1173025 c.1816delT p.S606fs*14 Deletion - Frameshift 4:15625286-15625286 - CSCC-55-T COSM4463953 c.1311C>T p.T437T Substitution - coding silent 4:15625791-15625791 - TCGA-AX-A05Z-01 COSM1052487 c.1747G>T p.D583Y Substitution - Missense 4:15625355-15625355 - CHC121T COSM3669259 c.1116A>T p.A372A Substitution - coding silent 4:15626881-15626881 - T3301 COSM4683893 c.1974C>G p.Y658* Substitution - Nonsense 4:15612291-15612291 - TCGA-B5-A0JY-01 COSM1052498 c.1182G>A p.E394E Substitution - coding silent 4:15625920-15625920 - TCGA-EI-6882-01 COSM3428268 c.944G>A p.R315H Substitution - Missense 4:15627982-15627982 - MDA-MB-468 COSM1670907 c.1055T>C p.L352S Substitution - Missense 4:15626942-15626942 - TCGA-B9-5156-01 COSM3993518 c.448A>G p.I150V Substitution - Missense 4:15638643-15638643 - Single_liver_8 COSM5783194 c.1654delT p.C552fs*6 Deletion - Frameshift 4:15625448-15625448 - Gp2D COSM4628265 c.1284A>G p.S428S Substitution - coding silent 4:15625818-15625818 - C0097T COSM4155021 c.424T>C p.F142L Substitution - Missense 4:15638667-15638667 - NCI-H322M COSM1194813 c.1289C>T p.A430V Substitution - Missense 4:15625813-15625813 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.643433 4p15.32 605655

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.H498Q c.1494T>G 4 15627231 CM A C Synonymous p.P579P c.1737T>G 4 15626988 BLCA A G Synonymous p.C546C c.1638T>C 4 15627087 CM AGTCTGGGTA - Frameshift p.Q365Ffs*34 c.1089_1098delTACCCAGACT 4 15628522 OV A T Missense p.N83K c.249T>A 4 15646167 LUAD C A Missense p.G597V c.1790G>T 4 15626935 GBM C A Missense p.S531I c.1592G>T 4 15627133 CM C A Missense p.W480C c.1440G>T 4 15627285 LUAD C A SpliceDonorSNV . c.1124+1G>T 4 15628495 SCLC C T Missense p.A544T c.1630G>A 4 15627095 UCEC C T Missense p.E691K c.2071G>A 4 15607351 STAD C T Missense p.G667S c.1999G>A 4 15613889 ESCA C T SpliceAcceptorSNV . c.584-1G>A 4 15638300 BRCA G A Missense p.A177V c.530C>T 4 15640184 CM G A Missense p.P579L c.1736C>T 4 15626989 PAAD G A Missense p.S304L c.911C>T 4 15629638 BRCA G A Nonsense p.Q135* c.403C>T 4 15640311 CM G A Nonsense p.R684* c.2050C>T 4 15607372 CM G A Synonymous p.F217F c.651C>T 4 15638232 BRCA G C Missense p.A484G c.1451C>G 4 15627274 DLBCL G C Missense p.Q161E c.481C>G 4 15640233 BRCA G C Missense p.S440C c.1319C>G 4 15627406 LUAD GG AA Missense p.P626F c.1876_1877delinsTT 4 15614011 CM G T Missense p.P477H c.1430C>A 4 15627295 BRCA G T Missense p.S81Y c.242C>A 4 15646174 HNSC T C 3-UTRSNV . c.2073+902A>G 4 15606447 HC T C Missense p.K434R c.1301A>G 4 15627424 LUSC T G Missense p.E281A c.842A>C 4 15632339 GBM