Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 15 76225142 76225142 + Missense_Mutation SNP C C A TCGA-OR-A5KP-01A-11D-A30A-10 TCGA-OR-A5KP-10A-01D-A30A-10 g.chr15:76225142C>A c.911C>A c.(910-912)gCt>gAt p.A304D ACC 15 76225297 76225297 + Missense_Mutation SNP G G A TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr15:76225297G>A c.1066G>A c.(1066-1068)Ggc>Agc p.G356S BLCA 15 76196329 76196329 + Missense_Mutation SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr15:76196329G>A c.25G>A c.(25-27)Gag>Aag p.E9K BLCA 15 76206478 76206478 + Missense_Mutation SNP C C T TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr15:76206478C>T c.395C>T c.(394-396)gCa>gTa p.A132V BLCA 15 76206519 76206519 + Missense_Mutation SNP C C G TCGA-FD-A3B5-01A-11D-A20D-08 TCGA-FD-A3B5-10A-01D-A20D-08 g.chr15:76206519C>G c.436C>G c.(436-438)Ctt>Gtt p.L146V BLCA 15 76222340 76222340 + Silent SNP C C T TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr15:76222340C>T c.744C>T c.(742-744)atC>atT p.I248I BLCA 15 76222343 76222343 + Missense_Mutation SNP C C G TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr15:76222343C>G c.747C>G c.(745-747)atC>atG p.I249M BLCA 15 76225119 76225119 + Silent SNP C C G TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr15:76225119C>G c.888C>G c.(886-888)gtC>gtG p.V296V BLCA 15 76225158 76225158 + Silent SNP C C T TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr15:76225158C>T c.927C>T c.(925-927)ctC>ctT p.L309L BLCA 15 76225218 76225218 + Silent SNP G G A TCGA-FD-A5BV-01A-11D-A26M-08 TCGA-FD-A5BV-10A-01D-A26K-08 g.chr15:76225218G>A c.987G>A c.(985-987)agG>agA p.R329R BLCA 15 76225291 76225291 + Missense_Mutation SNP T T G TCGA-C4-A0F0-01A-12D-A10S-08 TCGA-C4-A0F0-10A-01D-A10S-08 g.chr15:76225291T>G c.1060T>G c.(1060-1062)Tta>Gta p.L354V BRCA 15 76196845 76196845 + Missense_Mutation SNP T T C TCGA-A2-A0CT-01A-31W-A071-09 TCGA-A2-A0CT-10A-01W-A071-09 g.chr15:76196845T>C c.154T>C c.(154-156)Tgg>Cgg p.W52R BRCA 15 76222285 76222285 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr15:76222285T>G c.689T>G c.(688-690)gTg>gGg p.V230G BRCA 15 76225245 76225245 + Silent SNP G G C TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chr15:76225245G>C c.1014G>C c.(1012-1014)ggG>ggC p.G338G CESC 15 76209576 76209576 + Missense_Mutation SNP C C G TCGA-FU-A3HY-01A-11D-A21Q-09 TCGA-FU-A3HY-10A-01D-A21Q-09 g.chr15:76209576C>G c.469C>G c.(469-471)Cca>Gca p.P157A CESC 15 76209603 76209603 + Nonsense_Mutation SNP C C T TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr15:76209603C>T c.496C>T c.(496-498)Cag>Tag p.Q166* COAD 15 76196408 76196408 + Missense_Mutation SNP C C T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr15:76196408C>T c.104C>T c.(103-105)aCc>aTc p.T35I COAD 15 76209715 76209715 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:76209715G>T c.608G>T c.(607-609)aGa>aTa p.R203I COAD 15 76222308 76222308 + Nonsense_Mutation SNP C C T TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr15:76222308C>T c.712C>T c.(712-714)Caa>Taa p.Q238* COAD 15 76225214 76225214 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:76225214G>T c.983G>T c.(982-984)gGc>gTc p.G328V COAD 15 76225330 76225330 + Missense_Mutation SNP C C T TCGA-AA-A01T-01A-21W-A096-10 TCGA-AA-A01T-11A-11W-A096-10 g.chr15:76225330C>T c.1099C>T c.(1099-1101)Cgg>Tgg p.R367W COADREAD 15 76196408 76196408 + Missense_Mutation SNP C C T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr15:76196408C>T c.104C>T c.(103-105)aCc>aTc p.T35I COADREAD 15 76206460 76206460 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:76206460G>T c.377G>T c.(376-378)aGa>aTa p.R126I COADREAD 15 76209715 76209715 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:76209715G>T c.608G>T c.(607-609)aGa>aTa p.R203I COADREAD 15 76222308 76222308 + Nonsense_Mutation SNP C C T TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr15:76222308C>T c.712C>T c.(712-714)Caa>Taa p.Q238* COADREAD 15 76225214 76225214 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:76225214G>T c.983G>T c.(982-984)gGc>gTc p.G328V COADREAD 15 76225330 76225330 + Missense_Mutation SNP C C T TCGA-AA-A01T-01A-21W-A096-10 TCGA-AA-A01T-11A-11W-A096-10 g.chr15:76225330C>T c.1099C>T c.(1099-1101)Cgg>Tgg p.R367W DLBC 15 76205550 76205550 + Missense_Mutation SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr15:76205550C>T c.286C>T c.(286-288)Cgc>Tgc p.R96C ESCA 15 76222260 76222260 + Missense_Mutation SNP G G T TCGA-IG-A4P3-01A-11D-A27G-09 TCGA-IG-A4P3-10A-01D-A27G-09 g.chr15:76222260G>T c.664G>T c.(664-666)Gtc>Ttc p.V222F GBM 15 76196838 76196838 + Silent SNP C C T TCGA-28-2509-01A-01D-1494-08 TCGA-28-2509-10A-01D-1494-08 g.chr15:76196838C>T c.147C>T c.(145-147)tgC>tgT p.C49C GBM 15 76205599 76205599 + Frame_Shift_Del DEL T T - TCGA-06-0648-01A-01W-0323-08 TCGA-06-0648-10A-01W-0323-08 g.chr15:76205599delT c.335delT c.(334-336)attfs p.I112fs GBM 15 76225151 76225151 + Missense_Mutation SNP A A G TCGA-27-2521-01A-01D-1494-08 TCGA-27-2521-10A-01D-1494-08 g.chr15:76225151A>G c.920A>G c.(919-921)cAg>cGg p.Q307R GBMLGG 15 76196838 76196838 + Silent SNP C C T TCGA-28-2509-01A-01D-1494-08 TCGA-28-2509-10A-01D-1494-08 g.chr15:76196838C>T c.147C>T c.(145-147)tgC>tgT p.C49C GBMLGG 15 76205599 76205599 + Frame_Shift_Del DEL T T - TCGA-06-0648-01A-01W-0323-08 TCGA-06-0648-10A-01W-0323-08 g.chr15:76205599delT c.335delT c.(334-336)attfs p.I112fs GBMLGG 15 76222395 76222395 + Intron SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:76222395G>A GBMLGG 15 76225151 76225151 + Missense_Mutation SNP A A G TCGA-27-2521-01A-01D-1494-08 TCGA-27-2521-10A-01D-1494-08 g.chr15:76225151A>G c.920A>G c.(919-921)cAg>cGg p.Q307R KIPAN 15 76196905 76196905 + Missense_Mutation SNP G G A TCGA-B9-4117-01A-01D-1252-08 TCGA-B9-4117-10A-01D-1252-08 g.chr15:76196905G>A c.214G>A c.(214-216)Ggc>Agc p.G72S KIPAN 15 76222396 76222396 + Intron SNP T T A TCGA-B0-4706-01A-01D-1501-10 TCGA-B0-4706-11A-02D-1501-10 g.chr15:76222396T>A KIRC 15 76222396 76222396 + Intron SNP T T A TCGA-B0-4706-01A-01D-1501-10 TCGA-B0-4706-11A-02D-1501-10 g.chr15:76222396T>A KIRP 15 76196905 76196905 + Missense_Mutation SNP G G A TCGA-B9-4117-01A-01D-1252-08 TCGA-B9-4117-10A-01D-1252-08 g.chr15:76196905G>A c.214G>A c.(214-216)Ggc>Agc p.G72S LGG 15 76222395 76222395 + Intron SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:76222395G>A LIHC 15 76206465 76206465 + Missense_Mutation SNP A A G TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr15:76206465A>G c.382A>G c.(382-384)Agt>Ggt p.S128G LUAD 15 76205553 76205553 + Missense_Mutation SNP A A G TCGA-55-6970-01A-11D-1945-08 TCGA-55-6970-11A-01D-1945-08 g.chr15:76205553A>G c.289A>G c.(289-291)Atc>Gtc p.I97V LUAD 15 76222283 76222283 + Missense_Mutation SNP G G T TCGA-05-4384-01A-01D-1753-08 TCGA-05-4384-10A-01D-1753-08 g.chr15:76222283G>T c.687G>T c.(685-687)aaG>aaT p.K229N LUAD 15 76225419 76225422 + Frame_Shift_Del DEL CATA CATA - TCGA-97-7941-01A-11D-2184-08 TCGA-97-7941-10A-01D-2184-08 g.chr15:76225419_76225422delCATA c.1188_1191delCATA c.(1186-1191)ctcatafs p.LI396fs LUSC 15 76205551 76205551 + Missense_Mutation SNP G G A TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr15:76205551G>A c.287G>A c.(286-288)cGc>cAc p.R96H LUSC 15 76206519 76206519 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:76206519C>T c.436C>T c.(436-438)Ctt>Ttt p.L146F LUSC 15 76222290 76222290 + Missense_Mutation SNP G G A TCGA-34-2596-01A-01D-1522-08 TCGA-34-2596-11A-01D-1522-08 g.chr15:76222290G>A c.694G>A c.(694-696)Gcc>Acc p.A232T LUSC 15 76225331 76225331 + Missense_Mutation SNP G G T TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chr15:76225331G>T c.1100G>T c.(1099-1101)cGg>cTg p.R367L LUSC 15 76225414 76225414 + Missense_Mutation SNP G G T TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr15:76225414G>T c.1183G>T c.(1183-1185)Gca>Tca p.A395S LUSC 15 76225439 76225439 + Missense_Mutation SNP A A G TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr15:76225439A>G c.1208A>G c.(1207-1209)aAa>aGa p.K403R PAAD 15 76196872 76196872 + Missense_Mutation SNP C C T TCGA-HZ-A77O-01A-11D-A33T-08 TCGA-HZ-A77O-10A-01D-A33W-08 g.chr15:76196872C>T c.181C>T c.(181-183)Cgg>Tgg p.R61W READ 15 76206460 76206460 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:76206460G>T c.377G>T c.(376-378)aGa>aTa p.R126I SKCM 15 76205550 76205550 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:76205550C>T c.286C>T c.(286-288)Cgc>Tgc p.R96C SKCM 15 76225175 76225175 + Missense_Mutation SNP C C T TCGA-D3-A1QA-06A-11D-A196-08 TCGA-D3-A1QA-10A-01D-A198-08 g.chr15:76225175C>T c.944C>T c.(943-945)cCa>cTa p.P315L SKCM 15 76225279 76225279 + Missense_Mutation SNP C C T TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr15:76225279C>T c.1048C>T c.(1048-1050)Cct>Tct p.P350S SKCM 15 76225310 76225310 + Missense_Mutation SNP A A C TCGA-EE-A2GH-06A-11D-A196-08 TCGA-EE-A2GH-10A-01D-A198-08 g.chr15:76225310A>C c.1079A>C c.(1078-1080)aAt>aCt p.N360T

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 15 76196329 76196329 single base substitution G A 5_prime_UTR_variant BLCA-US 15 76196329 76196329 single base substitution G A exon_variant BLCA-US 15 76196329 76196329 single base substitution G A missense_variant E3K 7G>A BLCA-US 15 76196329 76196329 single base substitution G A missense_variant E9K 25G>A BLCA-US 15 76196329 76196329 single base substitution G A upstream_gene_variant BLCA-US 15 76206519 76206519 single base substitution C G 3_prime_UTR_variant BLCA-US 15 76206519 76206519 single base substitution C G downstream_gene_variant BLCA-US 15 76206519 76206519 single base substitution C G exon_variant BLCA-US 15 76206519 76206519 single base substitution C G intron_variant BLCA-US 15 76206519 76206519 single base substitution C G missense_variant L140V 418C>G BLCA-US 15 76206519 76206519 single base substitution C G missense_variant L146V 436C>G BLCA-US 15 76206519 76206519 single base substitution C G missense_variant L42V 124C>G BLCA-US 15 76222340 76222340 single base substitution C T 3_prime_UTR_variant BLCA-US 15 76222340 76222340 single base substitution C T exon_variant BLCA-US 15 76222340 76222340 single base substitution C T synonymous_variant I144I 432C>T BLCA-US 15 76222340 76222340 single base substitution C T synonymous_variant I187I 561C>T BLCA-US 15 76222340 76222340 single base substitution C T synonymous_variant I248I 744C>T BLCA-US 15 76222340 76222340 single base substitution C T upstream_gene_variant BLCA-US 15 76225291 76225291 single base substitution T G 3_prime_UTR_variant BLCA-US 15 76225291 76225291 single base substitution T G downstream_gene_variant BLCA-US 15 76225291 76225291 single base substitution T G intron_variant BLCA-US 15 76225291 76225291 single base substitution T G missense_variant L250V 748T>G BLCA-US 15 76225291 76225291 single base substitution T G missense_variant L354V 1060T>G BLCA-US 15 76225291 76225291 single base substitution T G missense_variant L51V 151T>G BOCA-FR 15 76226947 76226947 single base substitution G A 3_prime_UTR_variant BOCA-FR 15 76226947 76226947 single base substitution G A downstream_gene_variant BRCA-EU 15 76191560 76191560 single base substitution G A upstream_gene_variant BRCA-EU 15 76191644 76191644 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 76191949 76191949 single base substitution G C upstream_gene_variant BRCA-EU 15 76194129 76194129 single base substitution C G upstream_gene_variant BRCA-EU 15 76194874 76194874 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 76195013 76195013 single base substitution T A upstream_gene_variant BRCA-EU 15 76196132 76196132 single base substitution C G upstream_gene_variant BRCA-EU 15 76196829 76196829 single base substitution C T intron_variant BRCA-EU 15 76196829 76196829 single base substitution C T splice_region_variant BRCA-EU 15 76197281 76197281 single base substitution C A intron_variant BRCA-EU 15 76197405 76197405 single base substitution C A intron_variant BRCA-EU 15 76197817 76197817 single base substitution C G intron_variant BRCA-EU 15 76199374 76199374 deletion of <=200bp T - intron_variant BRCA-EU 15 76200296 76200296 single base substitution A T intron_variant BRCA-EU 15 76201932 76201932 single base substitution G C intron_variant BRCA-EU 15 76201932 76201932 single base substitution G C upstream_gene_variant BRCA-EU 15 76202076 76202076 single base substitution G A intron_variant BRCA-EU 15 76202076 76202076 single base substitution G A upstream_gene_variant BRCA-EU 15 76202667 76202667 single base substitution C T intron_variant BRCA-EU 15 76202667 76202667 single base substitution C T splice_region_variant BRCA-EU 15 76202667 76202667 single base substitution C T upstream_gene_variant BRCA-EU 15 76203048 76203048 single base substitution G T downstream_gene_variant BRCA-EU 15 76203048 76203048 single base substitution G T intron_variant BRCA-EU 15 76203048 76203048 single base substitution G T upstream_gene_variant BRCA-EU 15 76203162 76203162 single base substitution G C downstream_gene_variant BRCA-EU 15 76203162 76203162 single base substitution G C intron_variant BRCA-EU 15 76203162 76203162 single base substitution G C upstream_gene_variant BRCA-EU 15 76204008 76204008 single base substitution G A downstream_gene_variant BRCA-EU 15 76204008 76204008 single base substitution G A intron_variant BRCA-EU 15 76204008 76204008 single base substitution G A upstream_gene_variant BRCA-EU 15 76204080 76204080 single base substitution A G downstream_gene_variant BRCA-EU 15 76204080 76204080 single base substitution A G intron_variant BRCA-EU 15 76204080 76204080 single base substitution A G upstream_gene_variant BRCA-EU 15 76204823 76204823 single base substitution C T downstream_gene_variant BRCA-EU 15 76204823 76204823 single base substitution C T intron_variant BRCA-EU 15 76204823 76204823 single base substitution C T upstream_gene_variant BRCA-EU 15 76205219 76205219 single base substitution T C downstream_gene_variant BRCA-EU 15 76205219 76205219 single base substitution T C intron_variant BRCA-EU 15 76205219 76205219 single base substitution T C upstream_gene_variant BRCA-EU 15 76206909 76206909 single base substitution G C downstream_gene_variant BRCA-EU 15 76206909 76206909 single base substitution G C intron_variant BRCA-EU 15 76207380 76207380 single base substitution C T downstream_gene_variant BRCA-EU 15 76207380 76207380 single base substitution C T intron_variant BRCA-EU 15 76208005 76208005 single base substitution G C intron_variant BRCA-EU 15 76211141 76211141 single base substitution C G intron_variant BRCA-EU 15 76211477 76211477 deletion of <=200bp T - intron_variant BRCA-EU 15 76212689 76212689 single base substitution G A intron_variant BRCA-EU 15 76214124 76214124 single base substitution C A intron_variant BRCA-EU 15 76215282 76215282 single base substitution G T intron_variant BRCA-EU 15 76215283 76215283 single base substitution G T intron_variant BRCA-EU 15 76215505 76215505 single base substitution A T intron_variant BRCA-EU 15 76218545 76218545 single base substitution G A intron_variant BRCA-EU 15 76220519 76220519 single base substitution G T intron_variant BRCA-EU 15 76220519 76220519 single base substitution G T upstream_gene_variant BRCA-EU 15 76222474 76222474 single base substitution A C 3_prime_UTR_variant BRCA-EU 15 76222474 76222474 single base substitution A C downstream_gene_variant BRCA-EU 15 76222474 76222474 single base substitution A C intron_variant BRCA-EU 15 76222474 76222474 single base substitution A C upstream_gene_variant BRCA-EU 15 76222632 76222632 single base substitution T A 3_prime_UTR_variant BRCA-EU 15 76222632 76222632 single base substitution T A downstream_gene_variant BRCA-EU 15 76222632 76222632 single base substitution T A intron_variant BRCA-EU 15 76222632 76222632 single base substitution T A upstream_gene_variant BRCA-EU 15 76225580 76225580 single base substitution C T 3_prime_UTR_variant BRCA-EU 15 76225580 76225580 single base substitution C T downstream_gene_variant BRCA-EU 15 76225580 76225580 single base substitution C T intron_variant BRCA-EU 15 76226908 76226908 single base substitution C T 3_prime_UTR_variant BRCA-EU 15 76226908 76226908 single base substitution C T downstream_gene_variant BRCA-EU 15 76228383 76228383 single base substitution C T downstream_gene_variant BRCA-EU 15 76228596 76228596 single base substitution T C downstream_gene_variant BRCA-EU 15 76228899 76228899 single base substitution C G downstream_gene_variant BRCA-EU 15 76229413 76229413 single base substitution A G downstream_gene_variant BRCA-EU 15 76229902 76229902 single base substitution C G downstream_gene_variant BRCA-EU 15 76230307 76230307 single base substitution G A downstream_gene_variant BRCA-FR 15 76196132 76196132 single base substitution C G upstream_gene_variant BRCA-FR 15 76196829 76196829 single base substitution C T intron_variant BRCA-FR 15 76196829 76196829 single base substitution C T splice_region_variant BRCA-FR 15 76197281 76197281 single base substitution C A intron_variant BRCA-FR 15 76197817 76197817 single base substitution C G intron_variant BRCA-FR 15 76200296 76200296 single base substitution A T intron_variant BRCA-FR 15 76203162 76203162 single base substitution G C downstream_gene_variant BRCA-FR 15 76203162 76203162 single base substitution G C intron_variant BRCA-FR 15 76203162 76203162 single base substitution G C upstream_gene_variant BRCA-FR 15 76204080 76204080 single base substitution A G downstream_gene_variant BRCA-FR 15 76204080 76204080 single base substitution A G intron_variant BRCA-FR 15 76204080 76204080 single base substitution A G upstream_gene_variant BRCA-FR 15 76206909 76206909 single base substitution G C downstream_gene_variant BRCA-FR 15 76206909 76206909 single base substitution G C intron_variant BRCA-FR 15 76212689 76212689 single base substitution G A intron_variant BRCA-FR 15 76216386 76216386 single base substitution C T intron_variant BRCA-FR 15 76216892 76216892 single base substitution A G intron_variant BRCA-FR 15 76222632 76222632 single base substitution T A 3_prime_UTR_variant BRCA-FR 15 76222632 76222632 single base substitution T A downstream_gene_variant BRCA-FR 15 76222632 76222632 single base substitution T A intron_variant BRCA-FR 15 76222632 76222632 single base substitution T A upstream_gene_variant BRCA-UK 15 76198260 76198260 single base substitution C A intron_variant BRCA-UK 15 76205640 76205640 single base substitution C G downstream_gene_variant BRCA-UK 15 76205640 76205640 single base substitution C G intron_variant BRCA-UK 15 76226908 76226908 single base substitution C T 3_prime_UTR_variant BRCA-UK 15 76226908 76226908 single base substitution C T downstream_gene_variant BRCA-US 15 76196845 76196845 single base substitution T C 5_prime_UTR_variant BRCA-US 15 76196845 76196845 single base substitution T C exon_variant BRCA-US 15 76196845 76196845 single base substitution T C intron_variant BRCA-US 15 76196845 76196845 single base substitution T C missense_variant W46R 136T>C BRCA-US 15 76196845 76196845 single base substitution T C missense_variant W52R 154T>C BRCA-US 15 76222285 76222285 single base substitution T G 3_prime_UTR_variant BRCA-US 15 76222285 76222285 single base substitution T G exon_variant BRCA-US 15 76222285 76222285 single base substitution T G missense_variant V126G 377T>G BRCA-US 15 76222285 76222285 single base substitution T G missense_variant V169G 506T>G BRCA-US 15 76222285 76222285 single base substitution T G missense_variant V230G 689T>G BRCA-US 15 76222285 76222285 single base substitution T G upstream_gene_variant BRCA-US 15 76225245 76225245 single base substitution G C 3_prime_UTR_variant BRCA-US 15 76225245 76225245 single base substitution G C downstream_gene_variant BRCA-US 15 76225245 76225245 single base substitution G C intron_variant BRCA-US 15 76225245 76225245 single base substitution G C synonymous_variant G234G 702G>C BRCA-US 15 76225245 76225245 single base substitution G C synonymous_variant G338G 1014G>C BRCA-US 15 76225245 76225245 single base substitution G C synonymous_variant G35G 105G>C BTCA-JP 15 76205524 76205524 deletion of <=200bp T - downstream_gene_variant BTCA-JP 15 76205524 76205524 deletion of <=200bp T - intron_variant BTCA-JP 15 76205524 76205524 deletion of <=200bp T - upstream_gene_variant BTCA-JP 15 76205524 76205525 deletion of <=200bp TT - downstream_gene_variant BTCA-JP 15 76205524 76205525 deletion of <=200bp TT - intron_variant BTCA-JP 15 76205524 76205525 deletion of <=200bp TT - upstream_gene_variant BTCA-JP 15 76225431 76225431 single base substitution G A 3_prime_UTR_variant BTCA-JP 15 76225431 76225431 single base substitution G A downstream_gene_variant BTCA-JP 15 76225431 76225431 single base substitution G A intron_variant BTCA-JP 15 76225431 76225431 single base substitution G A synonymous_variant G296G 888G>A BTCA-JP 15 76225431 76225431 single base substitution G A synonymous_variant G400G 1200G>A CESC-US 15 76209576 76209576 single base substitution C G 3_prime_UTR_variant CESC-US 15 76209576 76209576 single base substitution C G exon_variant CESC-US 15 76209576 76209576 single base substitution C G intron_variant CESC-US 15 76209576 76209576 single base substitution C G missense_variant P157A 469C>G CESC-US 15 76209576 76209576 single base substitution C G missense_variant P53A 157C>G CESC-US 15 76209603 76209603 single base substitution C T 3_prime_UTR_variant CESC-US 15 76209603 76209603 single base substitution C T exon_variant CESC-US 15 76209603 76209603 single base substitution C T intron_variant CESC-US 15 76209603 76209603 single base substitution C T stop_gained Q166* 496C>T CESC-US 15 76209603 76209603 single base substitution C T stop_gained Q62* 184C>T CLLE-ES 15 76196600 76196600 single base substitution C T intron_variant CLLE-ES 15 76210663 76210663 single base substitution A G intron_variant CLLE-ES 15 76217952 76217952 single base substitution G A intron_variant COAD-US 15 76196408 76196408 single base substitution C T 5_prime_UTR_variant COAD-US 15 76196408 76196408 single base substitution C T exon_variant COAD-US 15 76196408 76196408 single base substitution C T missense_variant T29I 86C>T COAD-US 15 76196408 76196408 single base substitution C T missense_variant T35I 104C>T COAD-US 15 76196408 76196408 single base substitution C T upstream_gene_variant COAD-US 15 76222308 76222308 single base substitution C T 3_prime_UTR_variant COAD-US 15 76222308 76222308 single base substitution C T exon_variant COAD-US 15 76222308 76222308 single base substitution C T stop_gained Q134* 400C>T COAD-US 15 76222308 76222308 single base substitution C T stop_gained Q177* 529C>T COAD-US 15 76222308 76222308 single base substitution C T stop_gained Q238* 712C>T COAD-US 15 76222308 76222308 single base substitution C T upstream_gene_variant COCA-CN 15 76191910 76191910 single base substitution A C upstream_gene_variant COCA-CN 15 76209743 76209743 single base substitution A C intron_variant COCA-CN 15 76209743 76209743 single base substitution A C splice_region_variant COCA-CN 15 76225329 76225329 single base substitution T A 3_prime_UTR_variant COCA-CN 15 76225329 76225329 single base substitution T A downstream_gene_variant COCA-CN 15 76225329 76225329 single base substitution T A intron_variant COCA-CN 15 76225329 76225329 single base substitution T A missense_variant D262E 786T>A COCA-CN 15 76225329 76225329 single base substitution T A missense_variant D366E 1098T>A COCA-CN 15 76225329 76225329 single base substitution T A missense_variant D63E 189T>A ESAD-UK 15 76198919 76198919 single base substitution A G intron_variant ESAD-UK 15 76200296 76200296 single base substitution A T intron_variant ESAD-UK 15 76200520 76200529 deletion of <=200bp GAGTAAGAAA - intron_variant ESAD-UK 15 76200531 76200531 insertion of <=200bp - T intron_variant ESAD-UK 15 76203507 76203507 single base substitution G A downstream_gene_variant ESAD-UK 15 76203507 76203507 single base substitution G A intron_variant ESAD-UK 15 76203507 76203507 single base substitution G A upstream_gene_variant ESAD-UK 15 76203651 76203651 single base substitution G A downstream_gene_variant ESAD-UK 15 76203651 76203651 single base substitution G A intron_variant ESAD-UK 15 76203651 76203651 single base substitution G A upstream_gene_variant ESAD-UK 15 76205186 76205186 single base substitution A C downstream_gene_variant ESAD-UK 15 76205186 76205186 single base substitution A C intron_variant ESAD-UK 15 76205186 76205186 single base substitution A C upstream_gene_variant ESAD-UK 15 76206916 76206916 single base substitution C T downstream_gene_variant ESAD-UK 15 76206916 76206916 single base substitution C T intron_variant ESAD-UK 15 76207033 76207033 single base substitution G T downstream_gene_variant ESAD-UK 15 76207033 76207033 single base substitution G T intron_variant ESAD-UK 15 76209323 76209323 single base substitution A T intron_variant ESAD-UK 15 76212433 76212433 single base substitution T C intron_variant ESAD-UK 15 76214680 76214680 single base substitution C T intron_variant ESAD-UK 15 76215389 76215389 single base substitution T C intron_variant ESAD-UK 15 76225199 76225199 single base substitution T A 3_prime_UTR_variant ESAD-UK 15 76225199 76225199 single base substitution T A downstream_gene_variant ESAD-UK 15 76225199 76225199 single base substitution T A intron_variant ESAD-UK 15 76225199 76225199 single base substitution T A missense_variant M20K 59T>A ESAD-UK 15 76225199 76225199 single base substitution T A missense_variant M219K 656T>A ESAD-UK 15 76225199 76225199 single base substitution T A missense_variant M323K 968T>A ESAD-UK 15 76225921 76225921 single base substitution A T 3_prime_UTR_variant ESAD-UK 15 76225921 76225921 single base substitution A T downstream_gene_variant ESAD-UK 15 76225921 76225921 single base substitution A T intron_variant ESAD-UK 15 76226942 76226942 single base substitution G T 3_prime_UTR_variant ESAD-UK 15 76226942 76226942 single base substitution G T downstream_gene_variant ESAD-UK 15 76227360 76227360 single base substitution T C 3_prime_UTR_variant ESAD-UK 15 76227360 76227360 single base substitution T C downstream_gene_variant ESAD-UK 15 76228014 76228014 single base substitution C T downstream_gene_variant ESAD-UK 15 76228620 76228620 single base substitution G C downstream_gene_variant ESAD-UK 15 76228876 76228876 single base substitution A C downstream_gene_variant ESAD-UK 15 76230046 76230046 single base substitution C T downstream_gene_variant ESAD-UK 15 76231051 76231051 single base substitution G A downstream_gene_variant ESCA-CN 15 76191632 76191633 deletion of <=200bp AT - upstream_gene_variant ESCA-CN 15 76205589 76205589 single base substitution G A 3_prime_UTR_variant ESCA-CN 15 76205589 76205589 single base substitution G A downstream_gene_variant ESCA-CN 15 76205589 76205589 single base substitution G A intron_variant ESCA-CN 15 76205589 76205589 single base substitution G A missense_variant E103K 307G>A ESCA-CN 15 76205589 76205589 single base substitution G A missense_variant E109K 325G>A ESCA-CN 15 76205589 76205589 single base substitution G A missense_variant E5K 13G>A ESCA-CN 15 76205589 76205589 single base substitution G A upstream_gene_variant GBM-US 15 76196838 76196838 single base substitution C T 5_prime_UTR_variant GBM-US 15 76196838 76196838 single base substitution C T exon_variant GBM-US 15 76196838 76196838 single base substitution C T intron_variant GBM-US 15 76196838 76196838 single base substitution C T synonymous_variant C43C 129C>T GBM-US 15 76196838 76196838 single base substitution C T synonymous_variant C49C 147C>T GBM-US 15 76205599 76205599 deletion of <=200bp T - 3_prime_UTR_variant GBM-US 15 76205599 76205599 deletion of <=200bp T - downstream_gene_variant GBM-US 15 76205599 76205599 deletion of <=200bp T - frameshift_variant I106 GBM-US 15 76205599 76205599 deletion of <=200bp T - frameshift_variant I112 GBM-US 15 76205599 76205599 deletion of <=200bp T - frameshift_variant I8 GBM-US 15 76205599 76205599 deletion of <=200bp T - intron_variant GBM-US 15 76205599 76205599 deletion of <=200bp T - upstream_gene_variant GBM-US 15 76225151 76225151 single base substitution A G 3_prime_UTR_variant GBM-US 15 76225151 76225151 single base substitution A G downstream_gene_variant GBM-US 15 76225151 76225151 single base substitution A G intron_variant GBM-US 15 76225151 76225151 single base substitution A G missense_variant Q203R 608A>G GBM-US 15 76225151 76225151 single base substitution A G missense_variant Q307R 920A>G GBM-US 15 76225151 76225151 single base substitution A G missense_variant Q4R 11A>G KIRC-US 15 76222396 76222396 single base substitution T A 3_prime_UTR_variant KIRC-US 15 76222396 76222396 single base substitution T A downstream_gene_variant KIRC-US 15 76222396 76222396 single base substitution T A missense_variant V267D 800T>A KIRC-US 15 76222396 76222396 single base substitution T A splice_region_variant KIRC-US 15 76222396 76222396 single base substitution T A upstream_gene_variant KIRP-US 15 76225142 76225142 single base substitution C A 3_prime_UTR_variant KIRP-US 15 76225142 76225142 single base substitution C A downstream_gene_variant KIRP-US 15 76225142 76225142 single base substitution C A intron_variant KIRP-US 15 76225142 76225142 single base substitution C A missense_variant A1D 2C>A KIRP-US 15 76225142 76225142 single base substitution C A missense_variant A200D 599C>A KIRP-US 15 76225142 76225142 single base substitution C A missense_variant A304D 911C>A LICA-CN 15 76196835 76196835 single base substitution G T 5_prime_UTR_premature_start_codon_gain_variant LICA-CN 15 76196835 76196835 single base substitution G T exon_variant LICA-CN 15 76196835 76196835 single base substitution G T intron_variant LICA-CN 15 76196835 76196835 single base substitution G T synonymous_variant V42V 126G>T LICA-CN 15 76196835 76196835 single base substitution G T synonymous_variant V48V 144G>T LICA-CN 15 76209662 76209662 single base substitution A T 3_prime_UTR_variant LICA-CN 15 76209662 76209662 single base substitution A T exon_variant LICA-CN 15 76209662 76209662 single base substitution A T intron_variant LICA-CN 15 76209662 76209662 single base substitution A T synonymous_variant I185I 555A>T LICA-CN 15 76209662 76209662 single base substitution A T synonymous_variant I81I 243A>T LICA-FR 15 76208841 76208841 single base substitution T C intron_variant LICA-FR 15 76213378 76213378 single base substitution C T intron_variant LICA-FR 15 76213401 76213401 single base substitution A G intron_variant LICA-FR 15 76219364 76219364 deletion of <=200bp T - intron_variant LICA-FR 15 76225269 76225269 single base substitution A G 3_prime_UTR_variant LICA-FR 15 76225269 76225269 single base substitution A G downstream_gene_variant LICA-FR 15 76225269 76225269 single base substitution A G intron_variant LICA-FR 15 76225269 76225269 single base substitution A G synonymous_variant R242R 726A>G LICA-FR 15 76225269 76225269 single base substitution A G synonymous_variant R346R 1038A>G LICA-FR 15 76225269 76225269 single base substitution A G synonymous_variant R43R 129A>G LICA-FR 15 76227793 76227793 single base substitution A G downstream_gene_variant LINC-JP 15 76196258 76196258 single base substitution G A 5_prime_UTR_variant LINC-JP 15 76196258 76196258 single base substitution G A upstream_gene_variant LINC-JP 15 76220053 76220053 single base substitution A C intron_variant LINC-JP 15 76220448 76220448 single base substitution T C intron_variant LINC-JP 15 76220448 76220448 single base substitution T C upstream_gene_variant LINC-JP 15 76222308 76222308 single base substitution C T 3_prime_UTR_variant LINC-JP 15 76222308 76222308 single base substitution C T exon_variant LINC-JP 15 76222308 76222308 single base substitution C T stop_gained Q134* 400C>T LINC-JP 15 76222308 76222308 single base substitution C T stop_gained Q177* 529C>T LINC-JP 15 76222308 76222308 single base substitution C T stop_gained Q238* 712C>T LINC-JP 15 76222308 76222308 single base substitution C T upstream_gene_variant LINC-JP 15 76223872 76223872 single base substitution A T downstream_gene_variant LINC-JP 15 76223872 76223872 single base substitution A T intron_variant LINC-JP 15 76223872 76223872 single base substitution A T upstream_gene_variant LIRI-JP 15 76191938 76191938 single base substitution T C upstream_gene_variant LIRI-JP 15 76192150 76192150 single base substitution A G upstream_gene_variant LIRI-JP 15 76194294 76194294 single base substitution G A upstream_gene_variant LIRI-JP 15 76200312 76200312 single base substitution C G intron_variant LIRI-JP 15 76200514 76200514 single base substitution G T intron_variant LIRI-JP 15 76200517 76200517 single base substitution C T intron_variant LIRI-JP 15 76202892 76202892 single base substitution C T downstream_gene_variant LIRI-JP 15 76202892 76202892 single base substitution C T intron_variant LIRI-JP 15 76202892 76202892 single base substitution C T upstream_gene_variant LIRI-JP 15 76204900 76204900 single base substitution A T downstream_gene_variant LIRI-JP 15 76204900 76204900 single base substitution A T intron_variant LIRI-JP 15 76204900 76204900 single base substitution A T upstream_gene_variant LIRI-JP 15 76205193 76205193 single base substitution A G downstream_gene_variant LIRI-JP 15 76205193 76205193 single base substitution A G intron_variant LIRI-JP 15 76205193 76205193 single base substitution A G upstream_gene_variant LIRI-JP 15 76205471 76205471 single base substitution T G downstream_gene_variant LIRI-JP 15 76205471 76205471 single base substitution T G intron_variant LIRI-JP 15 76205471 76205471 single base substitution T G upstream_gene_variant LIRI-JP 15 76211204 76211204 single base substitution A G intron_variant LIRI-JP 15 76211358 76211358 single base substitution G A intron_variant LIRI-JP 15 76211527 76211527 single base substitution G T intron_variant LIRI-JP 15 76212071 76212071 single base substitution G A intron_variant LIRI-JP 15 76212098 76212098 single base substitution T C intron_variant LIRI-JP 15 76213194 76213194 single base substitution A T intron_variant LIRI-JP 15 76213195 76213195 single base substitution G T intron_variant LIRI-JP 15 76219475 76219475 single base substitution T C intron_variant LIRI-JP 15 76222734 76222734 single base substitution T G 3_prime_UTR_variant LIRI-JP 15 76222734 76222734 single base substitution T G downstream_gene_variant LIRI-JP 15 76222734 76222734 single base substitution T G intron_variant LIRI-JP 15 76222734 76222734 single base substitution T G upstream_gene_variant LIRI-JP 15 76223217 76223217 single base substitution A G downstream_gene_variant LIRI-JP 15 76223217 76223217 single base substitution A G intron_variant LIRI-JP 15 76223217 76223217 single base substitution A G upstream_gene_variant LIRI-JP 15 76226229 76226229 single base substitution A G 3_prime_UTR_variant LIRI-JP 15 76226229 76226229 single base substitution A G downstream_gene_variant LIRI-JP 15 76226229 76226229 single base substitution A G intron_variant LIRI-JP 15 76228850 76228850 single base substitution A G downstream_gene_variant LIRI-JP 15 76229023 76229023 single base substitution C A downstream_gene_variant LIRI-JP 15 76229143 76229143 single base substitution A G downstream_gene_variant LIRI-JP 15 76229345 76229345 single base substitution A C downstream_gene_variant LIRI-JP 15 76231611 76231611 single base substitution T G downstream_gene_variant LUSC-KR 15 76193254 76193254 single base substitution A T upstream_gene_variant LUSC-KR 15 76196709 76196709 single base substitution C T intron_variant LUSC-KR 15 76209482 76209482 single base substitution G T intron_variant LUSC-KR 15 76215951 76215951 single base substitution C G intron_variant LUSC-KR 15 76215955 76215955 single base substitution A G intron_variant LUSC-KR 15 76220802 76220802 single base substitution C G intron_variant LUSC-KR 15 76220802 76220802 single base substitution C G upstream_gene_variant LUSC-KR 15 76227916 76227916 single base substitution A T downstream_gene_variant LUSC-US 15 76205551 76205551 single base substitution G A 3_prime_UTR_variant LUSC-US 15 76205551 76205551 single base substitution G A 5_prime_UTR_variant LUSC-US 15 76205551 76205551 single base substitution G A downstream_gene_variant LUSC-US 15 76205551 76205551 single base substitution G A intron_variant LUSC-US 15 76205551 76205551 single base substitution G A missense_variant R90H 269G>A LUSC-US 15 76205551 76205551 single base substitution G A missense_variant R96H 287G>A LUSC-US 15 76205551 76205551 single base substitution G A upstream_gene_variant LUSC-US 15 76206519 76206519 single base substitution C T 3_prime_UTR_variant LUSC-US 15 76206519 76206519 single base substitution C T downstream_gene_variant LUSC-US 15 76206519 76206519 single base substitution C T exon_variant LUSC-US 15 76206519 76206519 single base substitution C T intron_variant LUSC-US 15 76206519 76206519 single base substitution C T missense_variant L140F 418C>T LUSC-US 15 76206519 76206519 single base substitution C T missense_variant L146F 436C>T LUSC-US 15 76206519 76206519 single base substitution C T missense_variant L42F 124C>T LUSC-US 15 76222290 76222290 single base substitution G A 3_prime_UTR_variant LUSC-US 15 76222290 76222290 single base substitution G A exon_variant LUSC-US 15 76222290 76222290 single base substitution G A missense_variant A128T 382G>A LUSC-US 15 76222290 76222290 single base substitution G A missense_variant A171T 511G>A LUSC-US 15 76222290 76222290 single base substitution G A missense_variant A232T 694G>A LUSC-US 15 76222290 76222290 single base substitution G A upstream_gene_variant LUSC-US 15 76225331 76225331 single base substitution G T 3_prime_UTR_variant LUSC-US 15 76225331 76225331 single base substitution G T downstream_gene_variant LUSC-US 15 76225331 76225331 single base substitution G T intron_variant LUSC-US 15 76225331 76225331 single base substitution G T missense_variant R263L 788G>T LUSC-US 15 76225331 76225331 single base substitution G T missense_variant R367L 1100G>T LUSC-US 15 76225331 76225331 single base substitution G T missense_variant R64L 191G>T LUSC-US 15 76225414 76225414 single base substitution G T 3_prime_UTR_variant LUSC-US 15 76225414 76225414 single base substitution G T downstream_gene_variant LUSC-US 15 76225414 76225414 single base substitution G T intron_variant LUSC-US 15 76225414 76225414 single base substitution G T missense_variant A291S 871G>T LUSC-US 15 76225414 76225414 single base substitution G T missense_variant A395S 1183G>T LUSC-US 15 76225439 76225439 single base substitution A G 3_prime_UTR_variant LUSC-US 15 76225439 76225439 single base substitution A G downstream_gene_variant LUSC-US 15 76225439 76225439 single base substitution A G intron_variant LUSC-US 15 76225439 76225439 single base substitution A G missense_variant K299R 896A>G LUSC-US 15 76225439 76225439 single base substitution A G missense_variant K403R 1208A>G MALY-DE 15 76194792 76194792 single base substitution C T upstream_gene_variant MALY-DE 15 76196426 76196426 single base substitution C T 5_prime_UTR_variant MALY-DE 15 76196426 76196426 single base substitution C T exon_variant MALY-DE 15 76196426 76196426 single base substitution C T missense_variant A35V 104C>T MALY-DE 15 76196426 76196426 single base substitution C T missense_variant A41V 122C>T MALY-DE 15 76196426 76196426 single base substitution C T upstream_gene_variant MALY-DE 15 76199148 76199148 single base substitution A T intron_variant MALY-DE 15 76217627 76217627 single base substitution G A intron_variant MALY-DE 15 76224275 76224275 single base substitution C T downstream_gene_variant MALY-DE 15 76224275 76224275 single base substitution C T intron_variant MALY-DE 15 76224275 76224275 single base substitution C T upstream_gene_variant MELA-AU 15 76191282 76191282 single base substitution T G upstream_gene_variant MELA-AU 15 76191349 76191349 single base substitution C T upstream_gene_variant MELA-AU 15 76191583 76191583 single base substitution T A upstream_gene_variant MELA-AU 15 76191616 76191616 insertion of <=200bp - A upstream_gene_variant MELA-AU 15 76192481 76192481 single base substitution C T upstream_gene_variant MELA-AU 15 76193881 76193881 single base substitution C T upstream_gene_variant MELA-AU 15 76194194 76194194 single base substitution C T upstream_gene_variant MELA-AU 15 76194303 76194303 single base substitution C T upstream_gene_variant MELA-AU 15 76194829 76194829 single base substitution C A upstream_gene_variant MELA-AU 15 76195335 76195335 single base substitution C T upstream_gene_variant MELA-AU 15 76195728 76195728 single base substitution A T upstream_gene_variant MELA-AU 15 76196287 76196287 single base substitution C T 5_prime_UTR_variant MELA-AU 15 76196287 76196287 single base substitution C T upstream_gene_variant MELA-AU 15 76197452 76197453 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 76198183 76198183 single base substitution A T intron_variant MELA-AU 15 76198977 76198977 single base substitution C T intron_variant MELA-AU 15 76199008 76199008 single base substitution G A intron_variant MELA-AU 15 76199101 76199101 single base substitution C T intron_variant MELA-AU 15 76200252 76200252 single base substitution C T intron_variant MELA-AU 15 76200296 76200296 single base substitution A T intron_variant MELA-AU 15 76201051 76201051 single base substitution C T intron_variant MELA-AU 15 76201051 76201051 single base substitution C T upstream_gene_variant MELA-AU 15 76201087 76201087 single base substitution T C intron_variant MELA-AU 15 76201087 76201087 single base substitution T C upstream_gene_variant MELA-AU 15 76201170 76201170 single base substitution C A intron_variant MELA-AU 15 76201170 76201170 single base substitution C A upstream_gene_variant MELA-AU 15 76201216 76201216 single base substitution C T intron_variant MELA-AU 15 76201216 76201216 single base substitution C T upstream_gene_variant MELA-AU 15 76201883 76201883 single base substitution C T intron_variant MELA-AU 15 76201883 76201883 single base substitution C T upstream_gene_variant MELA-AU 15 76202832 76202832 single base substitution T C downstream_gene_variant MELA-AU 15 76202832 76202832 single base substitution T C intron_variant MELA-AU 15 76202832 76202832 single base substitution T C upstream_gene_variant MELA-AU 15 76203409 76203409 single base substitution C T downstream_gene_variant MELA-AU 15 76203409 76203409 single base substitution C T intron_variant MELA-AU 15 76203409 76203409 single base substitution C T upstream_gene_variant MELA-AU 15 76203630 76203630 single base substitution C T downstream_gene_variant MELA-AU 15 76203630 76203630 single base substitution C T intron_variant MELA-AU 15 76203630 76203630 single base substitution C T upstream_gene_variant MELA-AU 15 76203727 76203727 single base substitution C T downstream_gene_variant MELA-AU 15 76203727 76203727 single base substitution C T intron_variant MELA-AU 15 76203727 76203727 single base substitution C T upstream_gene_variant MELA-AU 15 76203840 76203840 single base substitution C T downstream_gene_variant MELA-AU 15 76203840 76203840 single base substitution C T intron_variant MELA-AU 15 76203840 76203840 single base substitution C T upstream_gene_variant MELA-AU 15 76204281 76204281 single base substitution C T downstream_gene_variant MELA-AU 15 76204281 76204281 single base substitution C T intron_variant MELA-AU 15 76204281 76204281 single base substitution C T upstream_gene_variant MELA-AU 15 76207164 76207164 single base substitution T C downstream_gene_variant MELA-AU 15 76207164 76207164 single base substitution T C intron_variant MELA-AU 15 76207992 76207992 single base substitution C T intron_variant MELA-AU 15 76208116 76208116 single base substitution C T intron_variant MELA-AU 15 76208167 76208167 single base substitution G A intron_variant MELA-AU 15 76209477 76209477 single base substitution G A intron_variant MELA-AU 15 76209673 76209673 single base substitution C T 3_prime_UTR_variant MELA-AU 15 76209673 76209673 single base substitution C T exon_variant MELA-AU 15 76209673 76209673 single base substitution C T intron_variant MELA-AU 15 76209673 76209673 single base substitution C T missense_variant P189L 566C>T MELA-AU 15 76209673 76209673 single base substitution C T missense_variant P85L 254C>T MELA-AU 15 76209715 76209715 single base substitution G A 3_prime_UTR_variant MELA-AU 15 76209715 76209715 single base substitution G A exon_variant MELA-AU 15 76209715 76209715 single base substitution G A intron_variant MELA-AU 15 76209715 76209715 single base substitution G A missense_variant R203K 608G>A MELA-AU 15 76209715 76209715 single base substitution G A missense_variant R99K 296G>A MELA-AU 15 76211230 76211230 single base substitution C T intron_variant MELA-AU 15 76211598 76211598 single base substitution C T intron_variant MELA-AU 15 76212024 76212024 single base substitution C T intron_variant MELA-AU 15 76212399 76212399 single base substitution C T intron_variant MELA-AU 15 76212559 76212559 single base substitution T C intron_variant MELA-AU 15 76212942 76212942 single base substitution C T intron_variant MELA-AU 15 76214063 76214063 single base substitution C T intron_variant MELA-AU 15 76214072 76214072 single base substitution C T intron_variant MELA-AU 15 76214816 76214816 single base substitution G A intron_variant MELA-AU 15 76215759 76215759 single base substitution C T intron_variant MELA-AU 15 76216687 76216687 single base substitution G C intron_variant MELA-AU 15 76216729 76216729 single base substitution C T intron_variant MELA-AU 15 76216813 76216813 single base substitution T C intron_variant MELA-AU 15 76216842 76216842 single base substitution C T intron_variant MELA-AU 15 76216942 76216942 single base substitution C T intron_variant MELA-AU 15 76218130 76218130 single base substitution C T intron_variant MELA-AU 15 76218391 76218391 single base substitution T C intron_variant MELA-AU 15 76219035 76219035 single base substitution G A intron_variant MELA-AU 15 76219290 76219290 single base substitution G A intron_variant MELA-AU 15 76219386 76219386 single base substitution C T intron_variant MELA-AU 15 76219624 76219624 single base substitution C T intron_variant MELA-AU 15 76219870 76219870 single base substitution C T intron_variant MELA-AU 15 76220489 76220489 single base substitution G A intron_variant MELA-AU 15 76220489 76220489 single base substitution G A upstream_gene_variant MELA-AU 15 76221282 76221282 single base substitution C T intron_variant MELA-AU 15 76221282 76221282 single base substitution C T upstream_gene_variant MELA-AU 15 76222003 76222003 single base substitution A T intron_variant MELA-AU 15 76222003 76222003 single base substitution A T upstream_gene_variant MELA-AU 15 76222054 76222054 single base substitution C T intron_variant MELA-AU 15 76222054 76222054 single base substitution C T upstream_gene_variant MELA-AU 15 76222123 76222123 single base substitution C T intron_variant MELA-AU 15 76222123 76222123 single base substitution C T upstream_gene_variant MELA-AU 15 76222828 76222829 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 15 76222828 76222829 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 76222828 76222829 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 76222828 76222829 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 76223444 76223444 single base substitution C T downstream_gene_variant MELA-AU 15 76223444 76223444 single base substitution C T intron_variant MELA-AU 15 76223444 76223444 single base substitution C T upstream_gene_variant MELA-AU 15 76223880 76223880 single base substitution C T downstream_gene_variant MELA-AU 15 76223880 76223880 single base substitution C T intron_variant MELA-AU 15 76223880 76223880 single base substitution C T upstream_gene_variant MELA-AU 15 76224444 76224444 single base substitution C T downstream_gene_variant MELA-AU 15 76224444 76224444 single base substitution C T intron_variant MELA-AU 15 76224444 76224444 single base substitution C T upstream_gene_variant MELA-AU 15 76225110 76225110 single base substitution C T 3_prime_UTR_variant MELA-AU 15 76225110 76225110 single base substitution C T downstream_gene_variant MELA-AU 15 76225110 76225110 single base substitution C T intron_variant MELA-AU 15 76225110 76225110 single base substitution C T synonymous_variant N189N 567C>T MELA-AU 15 76225110 76225110 single base substitution C T synonymous_variant N232N 696C>T MELA-AU 15 76225110 76225110 single base substitution C T synonymous_variant N293N 879C>T MELA-AU 15 76225110 76225110 single base substitution C T upstream_gene_variant MELA-AU 15 76225279 76225279 single base substitution C T 3_prime_UTR_variant MELA-AU 15 76225279 76225279 single base substitution C T downstream_gene_variant MELA-AU 15 76225279 76225279 single base substitution C T intron_variant MELA-AU 15 76225279 76225279 single base substitution C T missense_variant P246S 736C>T MELA-AU 15 76225279 76225279 single base substitution C T missense_variant P350S 1048C>T MELA-AU 15 76225279 76225279 single base substitution C T missense_variant P47S 139C>T MELA-AU 15 76225330 76225330 single base substitution C T 3_prime_UTR_variant MELA-AU 15 76225330 76225330 single base substitution C T downstream_gene_variant MELA-AU 15 76225330 76225330 single base substitution C T intron_variant MELA-AU 15 76225330 76225330 single base substitution C T missense_variant R263W 787C>T MELA-AU 15 76225330 76225330 single base substitution C T missense_variant R367W 1099C>T MELA-AU 15 76225330 76225330 single base substitution C T missense_variant R64W 190C>T MELA-AU 15 76225392 76225392 single base substitution T G 3_prime_UTR_variant MELA-AU 15 76225392 76225392 single base substitution T G downstream_gene_variant MELA-AU 15 76225392 76225392 single base substitution T G intron_variant MELA-AU 15 76225392 76225392 single base substitution T G missense_variant F283L 849T>G MELA-AU 15 76225392 76225392 single base substitution T G missense_variant F387L 1161T>G MELA-AU 15 76226263 76226263 single base substitution T C 3_prime_UTR_variant MELA-AU 15 76226263 76226263 single base substitution T C downstream_gene_variant MELA-AU 15 76226263 76226263 single base substitution T C intron_variant MELA-AU 15 76226529 76226529 single base substitution C T 3_prime_UTR_variant MELA-AU 15 76226529 76226529 single base substitution C T downstream_gene_variant MELA-AU 15 76228231 76228232 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant MELA-AU 15 76228612 76228612 single base substitution C T downstream_gene_variant MELA-AU 15 76228753 76228753 single base substitution C T downstream_gene_variant MELA-AU 15 76229798 76229798 single base substitution C T downstream_gene_variant MELA-AU 15 76229819 76229819 single base substitution C T downstream_gene_variant MELA-AU 15 76230052 76230052 single base substitution C T downstream_gene_variant MELA-AU 15 76230264 76230265 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 76230292 76230293 multiple base substitution (>=2bp and <=200bp) GG AT downstream_gene_variant MELA-AU 15 76230599 76230600 multiple base substitution (>=2bp and <=200bp) CA TG downstream_gene_variant MELA-AU 15 76230974 76230974 single base substitution C T downstream_gene_variant MELA-AU 15 76231502 76231502 single base substitution C A downstream_gene_variant MELA-AU 15 76232164 76232164 single base substitution C T downstream_gene_variant MELA-AU 15 76232401 76232401 single base substitution C T downstream_gene_variant MELA-AU 15 76232557 76232557 single base substitution G A downstream_gene_variant ORCA-IN 15 76203580 76203580 single base substitution C G downstream_gene_variant ORCA-IN 15 76203580 76203580 single base substitution C G intron_variant ORCA-IN 15 76203580 76203580 single base substitution C G upstream_gene_variant ORCA-IN 15 76221171 76221171 single base substitution C G intron_variant ORCA-IN 15 76221171 76221171 single base substitution C G upstream_gene_variant ORCA-IN 15 76221477 76221477 single base substitution C G intron_variant ORCA-IN 15 76221477 76221477 single base substitution C G upstream_gene_variant OV-AU 15 76192067 76192067 single base substitution G C upstream_gene_variant OV-AU 15 76197226 76197226 single base substitution G A intron_variant OV-AU 15 76198469 76198469 single base substitution G A intron_variant OV-AU 15 76199383 76199383 single base substitution C G intron_variant OV-AU 15 76204104 76204104 single base substitution C G downstream_gene_variant OV-AU 15 76204104 76204104 single base substitution C G intron_variant OV-AU 15 76204104 76204104 single base substitution C G upstream_gene_variant OV-AU 15 76210264 76210264 single base substitution A G intron_variant OV-AU 15 76210265 76210265 single base substitution G T intron_variant OV-AU 15 76220869 76220869 single base substitution A G intron_variant OV-AU 15 76220869 76220869 single base substitution A G upstream_gene_variant PACA-AU 15 76194090 76194099 deletion of <=200bp CTGGAGACCC - upstream_gene_variant PACA-AU 15 76196158 76196158 single base substitution C A upstream_gene_variant PACA-AU 15 76201475 76201475 single base substitution C T intron_variant PACA-AU 15 76201475 76201475 single base substitution C T upstream_gene_variant PACA-AU 15 76201558 76201558 single base substitution G C intron_variant PACA-AU 15 76201558 76201558 single base substitution G C upstream_gene_variant PACA-AU 15 76210452 76210452 single base substitution C G intron_variant PACA-AU 15 76218722 76218722 single base substitution G A intron_variant PACA-AU 15 76221943 76221943 single base substitution G A intron_variant PACA-AU 15 76221943 76221943 single base substitution G A upstream_gene_variant PACA-AU 15 76221944 76221944 single base substitution T G intron_variant PACA-AU 15 76221944 76221944 single base substitution T G upstream_gene_variant PACA-AU 15 76223822 76223822 single base substitution A G downstream_gene_variant PACA-AU 15 76223822 76223822 single base substitution A G intron_variant PACA-AU 15 76223822 76223822 single base substitution A G upstream_gene_variant PACA-AU 15 76228736 76228736 single base substitution G T downstream_gene_variant PACA-AU 15 76232019 76232019 single base substitution T C downstream_gene_variant PACA-CA 15 76195426 76195426 single base substitution C T upstream_gene_variant PACA-CA 15 76197458 76197458 single base substitution C T intron_variant PACA-CA 15 76200860 76200860 single base substitution C T intron_variant PACA-CA 15 76200860 76200860 single base substitution C T upstream_gene_variant PACA-CA 15 76206877 76206877 single base substitution G T downstream_gene_variant PACA-CA 15 76206877 76206877 single base substitution G T intron_variant PACA-CA 15 76211299 76211299 deletion of <=200bp T - intron_variant PACA-CA 15 76213035 76213035 single base substitution G A intron_variant PACA-CA 15 76215733 76215733 insertion of <=200bp - T intron_variant PACA-CA 15 76220409 76220409 single base substitution G A intron_variant PACA-CA 15 76220409 76220409 single base substitution G A upstream_gene_variant PACA-CA 15 76224943 76224943 single base substitution G A downstream_gene_variant PACA-CA 15 76224943 76224943 single base substitution G A intron_variant PACA-CA 15 76224943 76224943 single base substitution G A upstream_gene_variant PACA-CA 15 76225866 76225866 single base substitution G A 3_prime_UTR_variant PACA-CA 15 76225866 76225866 single base substitution G A downstream_gene_variant PACA-CA 15 76225866 76225866 single base substitution G A intron_variant PACA-CA 15 76230073 76230073 single base substitution C G downstream_gene_variant PACA-CA 15 76230878 76230878 single base substitution G A downstream_gene_variant PAEN-AU 15 76211367 76211367 single base substitution C T intron_variant PAEN-AU 15 76218447 76218447 single base substitution T A intron_variant PAEN-AU 15 76218450 76218450 single base substitution T C intron_variant PAEN-AU 15 76219966 76219966 single base substitution G A intron_variant PAEN-AU 15 76226425 76226425 single base substitution C A 3_prime_UTR_variant PAEN-AU 15 76226425 76226425 single base substitution C A downstream_gene_variant PAEN-AU 15 76226425 76226425 single base substitution C A intron_variant PAEN-IT 15 76213632 76213632 single base substitution A T intron_variant PBCA-DE 15 76195790 76195790 single base substitution C T upstream_gene_variant PBCA-DE 15 76196355 76196355 single base substitution G A 5_prime_UTR_variant PBCA-DE 15 76196355 76196355 single base substitution G A exon_variant PBCA-DE 15 76196355 76196355 single base substitution G A synonymous_variant P11P 33G>A PBCA-DE 15 76196355 76196355 single base substitution G A synonymous_variant P17P 51G>A PBCA-DE 15 76196355 76196355 single base substitution G A upstream_gene_variant PBCA-DE 15 76203296 76203296 deletion of <=200bp G - downstream_gene_variant PBCA-DE 15 76203296 76203296 deletion of <=200bp G - intron_variant PBCA-DE 15 76203296 76203296 deletion of <=200bp G - upstream_gene_variant PBCA-DE 15 76208507 76208508 deletion of <=200bp CA - intron_variant PBCA-DE 15 76225395 76225395 single base substitution T A 3_prime_UTR_variant PBCA-DE 15 76225395 76225395 single base substitution T A downstream_gene_variant PBCA-DE 15 76225395 76225395 single base substitution T A intron_variant PBCA-DE 15 76225395 76225395 single base substitution T A missense_variant H284Q 852T>A PBCA-DE 15 76225395 76225395 single base substitution T A missense_variant H388Q 1164T>A PBCA-DE 15 76229555 76229555 deletion of <=200bp A - downstream_gene_variant PRAD-CA 15 76202791 76202791 single base substitution G T downstream_gene_variant PRAD-CA 15 76202791 76202791 single base substitution G T intron_variant PRAD-CA 15 76202791 76202791 single base substitution G T upstream_gene_variant PRAD-CA 15 76225827 76225827 single base substitution T C 3_prime_UTR_variant PRAD-CA 15 76225827 76225827 single base substitution T C downstream_gene_variant PRAD-CA 15 76225827 76225827 single base substitution T C intron_variant PRAD-UK 15 76192023 76192023 insertion of <=200bp - T upstream_gene_variant PRAD-UK 15 76227477 76227477 single base substitution C T 3_prime_UTR_variant PRAD-UK 15 76227477 76227477 single base substitution C T downstream_gene_variant PRAD-UK 15 76230945 76230945 single base substitution G A downstream_gene_variant PRAD-UK 15 76231715 76231715 single base substitution A T downstream_gene_variant RECA-EU 15 76198784 76198784 single base substitution A G intron_variant RECA-EU 15 76210628 76210628 single base substitution G A intron_variant RECA-EU 15 76213128 76213128 single base substitution T A intron_variant RECA-EU 15 76214514 76214514 single base substitution T C intron_variant RECA-EU 15 76228582 76228582 single base substitution C A downstream_gene_variant SKCA-BR 15 76192575 76192575 single base substitution C T upstream_gene_variant SKCA-BR 15 76195239 76195239 single base substitution A G upstream_gene_variant SKCA-BR 15 76195534 76195534 single base substitution C T upstream_gene_variant SKCA-BR 15 76195790 76195790 single base substitution C T upstream_gene_variant SKCA-BR 15 76197318 76197318 single base substitution C T intron_variant SKCA-BR 15 76199623 76199623 single base substitution T A intron_variant SKCA-BR 15 76200304 76200304 single base substitution A G intron_variant SKCA-BR 15 76202268 76202268 single base substitution C T intron_variant SKCA-BR 15 76202268 76202268 single base substitution C T upstream_gene_variant SKCA-BR 15 76206973 76206973 single base substitution T C downstream_gene_variant SKCA-BR 15 76206973 76206973 single base substitution T C intron_variant SKCA-BR 15 76209532 76209532 single base substitution A T intron_variant SKCA-BR 15 76215928 76215928 single base substitution T G intron_variant SKCA-BR 15 76219190 76219190 single base substitution C A intron_variant SKCA-BR 15 76219191 76219191 single base substitution C T intron_variant SKCA-BR 15 76220884 76220884 single base substitution C T intron_variant SKCA-BR 15 76220884 76220884 single base substitution C T upstream_gene_variant SKCA-BR 15 76229554 76229554 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 15 76229694 76229694 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 15 76232465 76232466 deletion of <=200bp AT - downstream_gene_variant SKCM-US 15 76191779 76191779 single base substitution C T upstream_gene_variant SKCM-US 15 76205550 76205550 single base substitution C T 3_prime_UTR_variant SKCM-US 15 76205550 76205550 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 15 76205550 76205550 single base substitution C T downstream_gene_variant SKCM-US 15 76205550 76205550 single base substitution C T intron_variant SKCM-US 15 76205550 76205550 single base substitution C T missense_variant R90C 268C>T SKCM-US 15 76205550 76205550 single base substitution C T missense_variant R96C 286C>T SKCM-US 15 76205550 76205550 single base substitution C T upstream_gene_variant SKCM-US 15 76209645 76209645 single base substitution C T 3_prime_UTR_variant SKCM-US 15 76209645 76209645 single base substitution C T exon_variant SKCM-US 15 76209645 76209645 single base substitution C T intron_variant SKCM-US 15 76209645 76209645 single base substitution C T missense_variant P180S 538C>T SKCM-US 15 76209645 76209645 single base substitution C T missense_variant P76S 226C>T SKCM-US 15 76225175 76225175 single base substitution C T 3_prime_UTR_variant SKCM-US 15 76225175 76225175 single base substitution C T downstream_gene_variant SKCM-US 15 76225175 76225175 single base substitution C T intron_variant SKCM-US 15 76225175 76225175 single base substitution C T missense_variant P12L 35C>T SKCM-US 15 76225175 76225175 single base substitution C T missense_variant P211L 632C>T SKCM-US 15 76225175 76225175 single base substitution C T missense_variant P315L 944C>T SKCM-US 15 76225224 76225224 single base substitution T C 3_prime_UTR_variant SKCM-US 15 76225224 76225224 single base substitution T C downstream_gene_variant SKCM-US 15 76225224 76225224 single base substitution T C intron_variant SKCM-US 15 76225224 76225224 single base substitution T C synonymous_variant F227F 681T>C SKCM-US 15 76225224 76225224 single base substitution T C synonymous_variant F28F 84T>C SKCM-US 15 76225224 76225224 single base substitution T C synonymous_variant F331F 993T>C SKCM-US 15 76225279 76225279 single base substitution C T 3_prime_UTR_variant SKCM-US 15 76225279 76225279 single base substitution C T downstream_gene_variant SKCM-US 15 76225279 76225279 single base substitution C T intron_variant SKCM-US 15 76225279 76225279 single base substitution C T missense_variant P246S 736C>T SKCM-US 15 76225279 76225279 single base substitution C T missense_variant P350S 1048C>T SKCM-US 15 76225279 76225279 single base substitution C T missense_variant P47S 139C>T SKCM-US 15 76225310 76225310 single base substitution A C 3_prime_UTR_variant SKCM-US 15 76225310 76225310 single base substitution A C downstream_gene_variant SKCM-US 15 76225310 76225310 single base substitution A C intron_variant SKCM-US 15 76225310 76225310 single base substitution A C missense_variant N256T 767A>C SKCM-US 15 76225310 76225310 single base substitution A C missense_variant N360T 1079A>C SKCM-US 15 76225310 76225310 single base substitution A C missense_variant N57T 170A>C STAD-US 15 76205620 76205620 single base substitution G A 3_prime_UTR_variant STAD-US 15 76205620 76205620 single base substitution G A downstream_gene_variant STAD-US 15 76205620 76205620 single base substitution G A exon_variant STAD-US 15 76205620 76205620 single base substitution G A intron_variant STAD-US 15 76205620 76205620 single base substitution G A missense_variant G113D 338G>A STAD-US 15 76205620 76205620 single base substitution G A missense_variant G119D 356G>A STAD-US 15 76205620 76205620 single base substitution G A missense_variant G15D 44G>A STAD-US 15 76222249 76222249 single base substitution G A 3_prime_UTR_variant STAD-US 15 76222249 76222249 single base substitution G A exon_variant STAD-US 15 76222249 76222249 single base substitution G A missense_variant R114H 341G>A STAD-US 15 76222249 76222249 single base substitution G A missense_variant R157H 470G>A STAD-US 15 76222249 76222249 single base substitution G A missense_variant R218H 653G>A STAD-US 15 76222249 76222249 single base substitution G A upstream_gene_variant STAD-US 15 76222269 76222269 single base substitution T C 3_prime_UTR_variant STAD-US 15 76222269 76222269 single base substitution T C exon_variant STAD-US 15 76222269 76222269 single base substitution T C missense_variant Y121H 361T>C STAD-US 15 76222269 76222269 single base substitution T C missense_variant Y164H 490T>C STAD-US 15 76222269 76222269 single base substitution T C missense_variant Y225H 673T>C STAD-US 15 76222269 76222269 single base substitution T C upstream_gene_variant STAD-US 15 76225165 76225165 single base substitution G A 3_prime_UTR_variant STAD-US 15 76225165 76225165 single base substitution G A downstream_gene_variant STAD-US 15 76225165 76225165 single base substitution G A intron_variant STAD-US 15 76225165 76225165 single base substitution G A missense_variant A208T 622G>A STAD-US 15 76225165 76225165 single base substitution G A missense_variant A312T 934G>A STAD-US 15 76225165 76225165 single base substitution G A missense_variant A9T 25G>A STAD-US 15 76225439 76225439 insertion of <=200bp - AAT 3_prime_UTR_variant STAD-US 15 76225439 76225439 insertion of <=200bp - AAT downstream_gene_variant STAD-US 15 76225439 76225439 insertion of <=200bp - AAT intron_variant STAD-US 15 76225439 76225439 insertion of <=200bp - AAT stop_gained K299K* STAD-US 15 76225439 76225439 insertion of <=200bp - AAT stop_gained K403K* UCEC-US 15 76191777 76191777 single base substitution C T upstream_gene_variant UCEC-US 15 76205550 76205550 single base substitution C T 3_prime_UTR_variant UCEC-US 15 76205550 76205550 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 15 76205550 76205550 single base substitution C T downstream_gene_variant UCEC-US 15 76205550 76205550 single base substitution C T intron_variant UCEC-US 15 76205550 76205550 single base substitution C T missense_variant R90C 268C>T UCEC-US 15 76205550 76205550 single base substitution C T missense_variant R96C 286C>T UCEC-US 15 76205550 76205550 single base substitution C T upstream_gene_variant UCEC-US 15 76205629 76205629 single base substitution G A downstream_gene_variant UCEC-US 15 76205629 76205629 single base substitution G A intron_variant UCEC-US 15 76205629 76205629 single base substitution G A missense_variant R116K 347G>A UCEC-US 15 76205629 76205629 single base substitution G A missense_variant R122K 365G>A UCEC-US 15 76205629 76205629 single base substitution G A missense_variant R18K 53G>A UCEC-US 15 76205629 76205629 single base substitution G A splice_region_variant UCEC-US 15 76206460 76206460 single base substitution G T 3_prime_UTR_variant UCEC-US 15 76206460 76206460 single base substitution G T downstream_gene_variant UCEC-US 15 76206460 76206460 single base substitution G T exon_variant UCEC-US 15 76206460 76206460 single base substitution G T intron_variant UCEC-US 15 76206460 76206460 single base substitution G T missense_variant R120I 359G>T UCEC-US 15 76206460 76206460 single base substitution G T missense_variant R126I 377G>T UCEC-US 15 76206460 76206460 single base substitution G T missense_variant R22I 65G>T UCEC-US 15 76206487 76206487 single base substitution T C 3_prime_UTR_variant UCEC-US 15 76206487 76206487 single base substitution T C downstream_gene_variant UCEC-US 15 76206487 76206487 single base substitution T C exon_variant UCEC-US 15 76206487 76206487 single base substitution T C intron_variant UCEC-US 15 76206487 76206487 single base substitution T C missense_variant L129P 386T>C UCEC-US 15 76206487 76206487 single base substitution T C missense_variant L135P 404T>C UCEC-US 15 76206487 76206487 single base substitution T C missense_variant L31P 92T>C UCEC-US 15 76209598 76209598 single base substitution G A 3_prime_UTR_variant UCEC-US 15 76209598 76209598 single base substitution G A exon_variant UCEC-US 15 76209598 76209598 single base substitution G A intron_variant UCEC-US 15 76209598 76209598 single base substitution G A missense_variant R164Q 491G>A UCEC-US 15 76209598 76209598 single base substitution G A missense_variant R60Q 179G>A UCEC-US 15 76222412 76222412 single base substitution T A 3_prime_UTR_variant UCEC-US 15 76222412 76222412 single base substitution T A downstream_gene_variant UCEC-US 15 76222412 76222412 single base substitution T A intron_variant UCEC-US 15 76222412 76222412 single base substitution T A missense_variant D272E 816T>A UCEC-US 15 76222412 76222412 single base substitution T A upstream_gene_variant UCEC-US 15 76225047 76225047 single base substitution C T 3_prime_UTR_variant UCEC-US 15 76225047 76225047 single base substitution C T downstream_gene_variant UCEC-US 15 76225047 76225047 single base substitution C T intron_variant UCEC-US 15 76225047 76225047 single base substitution C T synonymous_variant A168A 504C>T UCEC-US 15 76225047 76225047 single base substitution C T synonymous_variant A211A 633C>T UCEC-US 15 76225047 76225047 single base substitution C T synonymous_variant A272A 816C>T UCEC-US 15 76225047 76225047 single base substitution C T upstream_gene_variant UCEC-US 15 76225111 76225111 single base substitution G A 3_prime_UTR_variant UCEC-US 15 76225111 76225111 single base substitution G A downstream_gene_variant UCEC-US 15 76225111 76225111 single base substitution G A intron_variant UCEC-US 15 76225111 76225111 single base substitution G A missense_variant E190K 568G>A UCEC-US 15 76225111 76225111 single base substitution G A missense_variant E233K 697G>A UCEC-US 15 76225111 76225111 single base substitution G A missense_variant E294K 880G>A UCEC-US 15 76225111 76225111 single base substitution G A upstream_gene_variant UCEC-US 15 76225210 76225210 single base substitution G A 3_prime_UTR_variant UCEC-US 15 76225210 76225210 single base substitution G A downstream_gene_variant UCEC-US 15 76225210 76225210 single base substitution G A intron_variant UCEC-US 15 76225210 76225210 single base substitution G A missense_variant V223I 667G>A UCEC-US 15 76225210 76225210 single base substitution G A missense_variant V24I 70G>A UCEC-US 15 76225210 76225210 single base substitution G A missense_variant V327I 979G>A UCEC-US 15 76225245 76225245 single base substitution G A 3_prime_UTR_variant UCEC-US 15 76225245 76225245 single base substitution G A downstream_gene_variant UCEC-US 15 76225245 76225245 single base substitution G A intron_variant UCEC-US 15 76225245 76225245 single base substitution G A synonymous_variant G234G 702G>A UCEC-US 15 76225245 76225245 single base substitution G A synonymous_variant G338G 1014G>A UCEC-US 15 76225245 76225245 single base substitution G A synonymous_variant G35G 105G>A UCEC-US 15 76225317 76225317 single base substitution A C 3_prime_UTR_variant UCEC-US 15 76225317 76225317 single base substitution A C downstream_gene_variant UCEC-US 15 76225317 76225317 single base substitution A C intron_variant UCEC-US 15 76225317 76225317 single base substitution A C missense_variant E258D 774A>C UCEC-US 15 76225317 76225317 single base substitution A C missense_variant E362D 1086A>C UCEC-US 15 76225317 76225317 single base substitution A C missense_variant E59D 177A>C UCEC-US 15 76225324 76225324 single base substitution T C 3_prime_UTR_variant UCEC-US 15 76225324 76225324 single base substitution T C downstream_gene_variant UCEC-US 15 76225324 76225324 single base substitution T C intron_variant UCEC-US 15 76225324 76225324 single base substitution T C missense_variant C261R 781T>C UCEC-US 15 76225324 76225324 single base substitution T C missense_variant C365R 1093T>C UCEC-US 15 76225324 76225324 single base substitution T C missense_variant C62R 184T>C UCEC-US 15 76225330 76225330 single base substitution C T 3_prime_UTR_variant UCEC-US 15 76225330 76225330 single base substitution C T downstream_gene_variant UCEC-US 15 76225330 76225330 single base substitution C T intron_variant UCEC-US 15 76225330 76225330 single base substitution C T missense_variant R263W 787C>T UCEC-US 15 76225330 76225330 single base substitution C T missense_variant R367W 1099C>T UCEC-US 15 76225330 76225330 single base substitution C T missense_variant R64W 190C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-FW-A3R5-06 COSM965079 c.286C>T p.R96C Substitution - Missense 15:75913209-75913209 + TCGA-A2-A0CT-01 COSM434337 c.154T>C p.W52R Substitution - Missense 15:75904504-75904504 + TCGA-EE-A2GH-06 COSM3504153 c.1079A>C p.N360T Substitution - Missense 15:75932969-75932969 + TCGA-BH-A2L8-01 COSM3816786 c.1014G>C p.G338G Substitution - coding silent 15:75932904-75932904 + TCGA-B9-A5W8-01 COSM3988137 c.911C>A p.A304D Substitution - Missense 15:75932801-75932801 + HN_62740 COSM127980 c.420C>T p.P140P Substitution - coding silent 15:75914162-75914162 + TCGA-66-2782-01 COSM701822 c.1208A>G p.K403R Substitution - Missense 15:75933098-75933098 + TCGA-D9-A4Z3-01 COSM3504152 c.993T>C p.F331F Substitution - coding silent 15:75932883-75932883 + PD11344a COSM5798716 c.141-3C>T p.? Unknown 15:75904488-75904488 + S02360 COSM5696023 c.225G>A p.E75E Substitution - coding silent 15:75904575-75904575 + TCGA-AA-A010-01 COSM281092 c.983G>T p.G328V Substitution - Missense 15:75932873-75932873 + YUGURT COSM234238 c.856C>T p.Q286* Substitution - Nonsense 15:75932746-75932746 + TCGA-27-2521-01 COSM3401934 c.920A>G p.Q307R Substitution - Missense 15:75932810-75932810 + LUAD-5V8LT COSM401579 c.230G>T p.G77V Substitution - Missense 15:75904580-75904580 + TCGA-B5-A11J-01 COSM965085 c.880G>A p.E294K Substitution - Missense 15:75932770-75932770 + TCGA-66-2763-01 COSM701824 c.1100G>T p.R367L Substitution - Missense 15:75932990-75932990 + SC_9103 COSM5565382 c.851G>A p.R284Q Substitution - Missense 15:75932741-75932741 + TCGA-AA-A01T-01 COSM300223 c.1099C>T p.R367W Substitution - Missense 15:75932989-75932989 + LUAD-S01304 COSM385420 c.1014G>A p.G338G Substitution - coding silent 15:75932904-75932904 + 587376 COSM965086 c.979G>A p.V327I Substitution - Missense 15:75932869-75932869 + TCGA-C4-A0F0-01 COSM416807 c.1060T>G p.L354V Substitution - Missense 15:75932950-75932950 + TCGA-G2-A2ES-01 COSM1301455 c.744C>T p.I248I Substitution - coding silent 15:75929999-75929999 + Capan-1 COSM328355 c.685A>G p.K229E Substitution - Missense 15:75929940-75929940 + TCGA-FS-A1ZQ-06 COSM3887518 c.1048C>T p.P350S Substitution - Missense 15:75932938-75932938 + HCC159T COSM5806640 c.144G>T p.V48V Substitution - coding silent 15:75904494-75904494 + T613 COSM965086 c.979G>A p.V327I Substitution - Missense 15:75932869-75932869 + LC_C13 COSM1189072 c.20G>T p.C7F Substitution - Missense 15:75903983-75903983 + HT115 COSM177421 c.377G>T p.R126I Substitution - Missense 15:75914119-75914119 + TCGA-AA-A010-01 COSM281091 c.608G>T p.R203I Substitution - Missense 15:75917374-75917374 + TCGA-D3-A1QA-06 COSM3504151 c.944C>T p.P315L Substitution - Missense 15:75932834-75932834 + TCGA-BG-A0MQ-01 COSM300223 c.1099C>T p.R367W Substitution - Missense 15:75932989-75932989 + HCC35 COSM1374656 c.712C>T p.Q238* Substitution - Nonsense 15:75929967-75929967 + ESO-720 COSM1252264 c.170G>A p.R57H Substitution - Missense 15:75904520-75904520 + 93 COSM5015320 c.659T>C p.V220A Substitution - Missense 15:75929914-75929914 + TCGA-AA-3495-01 COSM5097979 c.850C>T p.R284* Substitution - Nonsense 15:75932740-75932740 + SC_9076 COSM5573526 c.628+2T>A p.? Unknown 15:75917396-75917396 + TCGA-06-0648 COSM2151380 c.335delT p.S113fs*37 Deletion - Frameshift 15:75913258-75913258 + sysucc-311T COSM5478976 c.628+8A>C p.? Unknown 15:75917402-75917402 + YUPROST COSM1708419 c.571C>T p.H191Y Substitution - Missense 15:75917337-75917337 + TCGA-CM-6168-01 COSM1374656 c.712C>T p.Q238* Substitution - Nonsense 15:75929967-75929967 + TCGA-D1-A17Q-01 COSM965082 c.491G>A p.R164Q Substitution - Missense 15:75917257-75917257 + TCGA-B5-A0JY-01 COSM177421 c.377G>T p.R126I Substitution - Missense 15:75914119-75914119 + TCGA-BR-4184-01 COSM4057030 c.356G>A p.G119D Substitution - Missense 15:75913279-75913279 + TCGA-EB-A431-01 COSM3504149 c.538C>T p.P180S Substitution - Missense 15:75917304-75917304 + HH14 COSM3728063 c.493C>T p.P165S Substitution - Missense 15:75917259-75917259 + ZZUFHECRKL-G054T COSM5445422 c.325G>A p.E109K Substitution - Missense 15:75913248-75913248 + tumor_4176133 COSM3356781 c.122C>T p.A41V Substitution - Missense 15:75904085-75904085 + TCGA-BS-A0UV-01 COSM965082 c.491G>A p.R164Q Substitution - Missense 15:75917257-75917257 + HCC2998 COSM1939696 c.591G>T p.K197N Substitution - Missense 15:75917357-75917357 + TCGA-28-2509-01 COSM3401932 c.147C>T p.C49C Substitution - coding silent 15:75904497-75904497 + TCGA-D1-A17Q-01 COSM965079 c.286C>T p.R96C Substitution - Missense 15:75913209-75913209 + TCGA-FU-A3HY-01 COSM4838641 c.469C>G p.P157A Substitution - Missense 15:75917235-75917235 + TCGA-AX-A05Z-01 COSM385420 c.1014G>A p.G338G Substitution - coding silent 15:75932904-75932904 + I2L-P8-Tumor-Biopsy COSM5363186 c.284T>G p.V95G Substitution - Missense 15:75913207-75913207 + TCGA-AP-A051-01 COSM965088 c.1093T>C p.C365R Substitution - Missense 15:75932983-75932983 + TCGA-BG-A18A-01 COSM965081 c.404T>C p.L135P Substitution - Missense 15:75914146-75914146 + HCC098T COSM5806640 c.144G>T p.V48V Substitution - coding silent 15:75904494-75904494 + TCGA-AX-A05Z-01 COSM965080 c.365G>A p.R122K Substitution - Missense 15:75913288-75913288 + TCGA-BS-A0UF-01 COSM965087 c.1086A>C p.E362D Substitution - Missense 15:75932976-75932976 + DN1122F COSM5798716 c.141-3C>T p.? Unknown 15:75904488-75904488 + TCGA-EK-A2R8-01 COSM4822511 c.496C>T p.Q166* Substitution - Nonsense 15:75917262-75917262 + TCGA-CK-4951-01 COSM1939715 c.1183G>A p.A395T Substitution - Missense 15:75933073-75933073 + HCC058T COSM5805189 c.555A>T p.I185I Substitution - coding silent 15:75917321-75917321 + PT16_1 COSM5898503 c.274C>T p.L92F Substitution - Missense 15:75904624-75904624 + CSCC-38-T COSM4455912 c.952A>T p.N318Y Substitution - Missense 15:75932842-75932842 + HN_0-046 COSM123120 c.112C>T p.P38S Substitution - Missense 15:75904075-75904075 + BCM711T COSM4956011 c.1038A>G p.R346R Substitution - coding silent 15:75932928-75932928 + TCGA-FD-A3B5-01 COSM1301453 c.436C>G p.L146V Substitution - Missense 15:75914178-75914178 + LAU165 COSM234238 c.856C>T p.Q286* Substitution - Nonsense 15:75932746-75932746 + TCGA-BR-4361-01 COSM4057034 c.673T>C p.Y225H Substitution - Missense 15:75929928-75929928 + BCM711T COSM4956011 c.1038A>G p.R346R Substitution - coding silent 15:75932928-75932928 + PT33 COSM5909428 c.469C>T p.P157S Substitution - Missense 15:75917235-75917235 + TCGA-B0-4706-01 COSM471087 c.794+6T>A p.? Unknown 15:75930055-75930055 + TCGA-BR-4370-01 COSM4057036 c.934G>A p.A312T Substitution - Missense 15:75932824-75932824 + PT33 COSM5909426 c.470C>T p.P157L Substitution - Missense 15:75917236-75917236 + SC_9034 COSM5556761 c.246T>C p.H82H Substitution - coding silent 15:75904596-75904596 + T3048 COSM701828 c.287G>A p.R96H Substitution - Missense 15:75913210-75913210 + CSCC-49-T COSM4538999 c.262G>A p.V88I Substitution - Missense 15:75904612-75904612 + PT23_2 COSM5903872 c.795-4C>T p.? Unknown 15:75932681-75932681 + LUAD-NYU575 COSM374997 c.162G>T p.E54D Substitution - Missense 15:75904512-75904512 + TCGA-BR-4362-01 COSM4057032 c.653G>A p.R218H Substitution - Missense 15:75929908-75929908 + TCGA-43-6143-01 COSM701823 c.1183G>T p.A395S Substitution - Missense 15:75933073-75933073 + TCGA-G4-6310-01 COSM1374654 c.104C>T p.T35I Substitution - Missense 15:75904067-75904067 + TCGA-A8-A0A6-01 COSM3816784 c.689T>G p.V230G Substitution - Missense 15:75929944-75929944 + TCGA-B5-A11N-01 COSM965086 c.979G>A p.V327I Substitution - Missense 15:75932869-75932869 + HCC35T COSM1374656 c.712C>T p.Q238* Substitution - Nonsense 15:75929967-75929967 + sysucc-1370T COSM5470400 c.1098T>A p.D366E Substitution - Missense 15:75932988-75932988 + TCGA-DK-A3WW-01 COSM3794415 c.25G>A p.E9K Substitution - Missense 15:75903988-75903988 + TCGA-AP-A059-01 COSM965084 c.816C>T p.A272A Substitution - coding silent 15:75932706-75932706 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.591115 15q24.2 609096

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.N360T c.1079A>C 15 76225310 CM A G IntronicSNV . c.628+928A>G 15 76210663 CLL A G Missense p.K403R c.1208A>G 15 76225439 LUSC A G Missense p.Q307R c.920A>G 15 76225151 GBM C G Missense p.L146V c.436C>G 15 76206519 BLCA C T Missense p.P180S c.538C>T 15 76209645 CM C T Missense p.P315L c.944C>T 15 76225175 CM C T Missense p.P350S c.1048C>T 15 76225279 CM C T Missense p.P38S c.112C>T 15 76196416 HNSC C T Missense p.R367W c.1099C>T 15 76225330 COREAD C T Missense p.R367W c.1099C>T 15 76225330 UCEC C T Synonymous p.C49C c.147C>T 15 76196838 GBM C T Synonymous p.I248I c.744C>T 15 76222340 BLCA C T Synonymous p.P140P c.420C>T 15 76206503 HNSC G A Missense p.A232T c.694G>A 15 76222290 LUSC G A Missense p.A312T c.934G>A 15 76225165 STAD G A Missense p.E294K c.880G>A 15 76225111 UCEC G A Missense p.R57H c.170G>A 15 76196861 ESCA G A Missense p.R96H c.287G>A 15 76205551 LUSC G T Missense p.A395S c.1183G>T 15 76225414 LUSC G T Missense p.K229N c.687G>T 15 76222283 LUAD G T Missense p.R367L c.1100G>T 15 76225331 LUSC T A IntronicSNV . c.794+22T>A 15 76222412 UCEC T A IntronicSNV . c.794+6T>A 15 76222396 RCCC T C Missense p.L135P c.404T>C 15 76206487 UCEC T C Missense p.W52R c.154T>C 15 76196845 BRCA T - Frameshift p.S113Vfs*37 c.336delT 15 76205599 GBM T G Missense p.L354V c.1060T>G 15 76225291 BLCA - T IntronicInsertion . c.279+212dupT 15 76197168 CM - TT IntronicInsertion . c.279+211_279+212dupTT 15 76197168 CM