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 43256191 43256191 + Missense_Mutation SNP T T C TCGA-OR-A5K8-01A-11D-A29I-10 TCGA-OR-A5K8-10A-01D-A29L-10 g.chr15:43256191T>C c.4642A>G c.(4642-4644)Aca>Gca p.T1548A BLCA 15 43242520 43242520 + Missense_Mutation SNP C C G TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr15:43242520C>G c.5048G>C c.(5047-5049)aGa>aCa p.R1683T BLCA 15 43258414 43258414 + Missense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr15:43258414G>A c.4528C>T c.(4528-4530)Cgc>Tgc p.R1510C BLCA 15 43281096 43281096 + Missense_Mutation SNP C C G TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr15:43281096C>G c.3918G>C c.(3916-3918)ttG>ttC p.L1306F BLCA 15 43294805 43294805 + Silent SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr15:43294805G>A c.3607C>T c.(3607-3609)Ctg>Ttg p.L1203L BLCA 15 43294862 43294862 + Missense_Mutation SNP G G A TCGA-FD-A3SO-01A-11D-A22Z-08 TCGA-FD-A3SO-10A-01D-A22Z-08 g.chr15:43294862G>A c.3550C>T c.(3550-3552)Cat>Tat p.H1184Y BLCA 15 43307928 43307928 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr15:43307928G>A c.3167C>T c.(3166-3168)tCa>tTa p.S1056L BLCA 15 43313566 43313566 + Silent SNP T T C TCGA-K4-A6FZ-01A-11D-A31L-08 TCGA-K4-A6FZ-10A-01D-A31J-08 g.chr15:43313566T>C c.2847A>G c.(2845-2847)ggA>ggG p.G949G BLCA 15 43317141 43317141 + Silent SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr15:43317141G>A c.2625C>T c.(2623-2625)ttC>ttT p.F875F BLCA 15 43328411 43328411 + Nonsense_Mutation SNP C C A TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr15:43328411C>A c.2155G>T c.(2155-2157)Gag>Tag p.E719* BLCA 15 43328427 43328427 + Silent SNP C C T TCGA-K4-A6FZ-01A-11D-A31L-08 TCGA-K4-A6FZ-10A-01D-A31J-08 g.chr15:43328427C>T c.2139G>A c.(2137-2139)caG>caA p.Q713Q BLCA 15 43330394 43330394 + Nonsense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr15:43330394G>C c.1886C>G c.(1885-1887)tCa>tGa p.S629* BLCA 15 43339379 43339379 + Nonsense_Mutation SNP G G A TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr15:43339379G>A c.1648C>T c.(1648-1650)Caa>Taa p.Q550* BLCA 15 43339380 43339380 + Missense_Mutation SNP G G T TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr15:43339380G>T c.1647C>A c.(1645-1647)ttC>ttA p.F549L BLCA 15 43339472 43339472 + Nonsense_Mutation SNP G G A TCGA-CF-A1HS-01A-11D-A13W-08 TCGA-CF-A1HS-10A-01D-A13W-08 g.chr15:43339472G>A c.1555C>T c.(1555-1557)Cga>Tga p.R519* BLCA 15 43351354 43351354 + Missense_Mutation SNP C C G TCGA-XF-A9SM-01A-11D-A42E-08 TCGA-XF-A9SM-10A-01D-A42H-08 g.chr15:43351354C>G c.1022G>C c.(1021-1023)aGa>aCa p.R341T BLCA 15 43360220 43360220 + Missense_Mutation SNP C C G TCGA-DK-A2I1-01A-11D-A17V-08 TCGA-DK-A2I1-10A-01D-A17V-08 g.chr15:43360220C>G c.674G>C c.(673-675)aGa>aCa p.R225T BLCA 15 43367196 43367196 + Missense_Mutation SNP C C G TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr15:43367196C>G c.509G>C c.(508-510)aGa>aCa p.R170T BRCA 15 43244537 43244537 + Missense_Mutation SNP C C G TCGA-E2-A108-01A-13D-A10M-09 TCGA-E2-A108-10A-01D-A10M-09 g.chr15:43244537C>G c.4945G>C c.(4945-4947)Gag>Cag p.E1649Q BRCA 15 43269025 43269026 + Missense_Mutation DNP TC TC AT TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr15:43269025_43269026TC>AT c.4258_4259GA>AT c.(4258-4260)GAc>ATc p.D1420I BRCA 15 43281144 43281144 + Missense_Mutation SNP G G C TCGA-EW-A1J5-01A-11D-A13L-09 TCGA-EW-A1J5-10A-01D-A13O-09 g.chr15:43281144G>C c.3870C>G c.(3868-3870)atC>atG p.I1290M BRCA 15 43282235 43282235 + Missense_Mutation SNP C C T TCGA-A8-A092-01A-11W-A019-09 TCGA-A8-A092-10A-01W-A021-09 g.chr15:43282235C>T c.3841G>A c.(3841-3843)Gag>Aag p.E1281K BRCA 15 43347026 43347026 + Missense_Mutation SNP C C A TCGA-AO-A0JB-01A-11W-A071-09 TCGA-AO-A0JB-10A-01W-A071-09 g.chr15:43347026C>A c.1353G>T c.(1351-1353)gaG>gaT p.E451D BRCA 15 43348619 43348619 + Nonsense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr15:43348619C>A c.1204G>T c.(1204-1206)Gaa>Taa p.E402* BRCA 15 43360113 43360113 + Missense_Mutation SNP T T C TCGA-A7-A4SF-01A-11D-A25Q-09 TCGA-A7-A4SF-10A-01D-A25Q-09 g.chr15:43360113T>C c.781A>G c.(781-783)Act>Gct p.T261A BRCA 15 43363018 43363018 + Missense_Mutation SNP C C T TCGA-E2-A2P6-01A-11D-A19Y-09 TCGA-E2-A2P6-10B-01D-A19Y-09 g.chr15:43363018C>T c.634G>A c.(634-636)Gaa>Aaa p.E212K BRCA 15 43363024 43363024 + Missense_Mutation SNP C C T TCGA-E2-A2P6-01A-11D-A19Y-09 TCGA-E2-A2P6-10B-01D-A19Y-09 g.chr15:43363024C>T c.628G>A c.(628-630)Gaa>Aaa p.E210K CESC 15 43270092 43270092 + Silent SNP G G A TCGA-Q1-A73P-01A-11D-A32I-09 TCGA-Q1-A73P-10B-01D-A32I-09 g.chr15:43270092G>A c.4204C>T c.(4204-4206)Ctg>Ttg p.L1402L CESC 15 43329982 43329982 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr15:43329982G>C c.2011C>G c.(2011-2013)Ctt>Gtt p.L671V CESC 15 43330009 43330009 + Missense_Mutation SNP C C T TCGA-MU-A51Y-01A-11D-A26G-09 TCGA-MU-A51Y-10A-01D-A26G-09 g.chr15:43330009C>T c.1984G>A c.(1984-1986)Gag>Aag p.E662K CESC 15 43335480 43335480 + Silent SNP T T C TCGA-R2-A69V-01A-11D-A32I-09 TCGA-R2-A69V-10A-01D-A32I-09 g.chr15:43335480T>C c.1782A>G c.(1780-1782)gaA>gaG p.E594E CHOL 15 43244513 43244513 + Missense_Mutation SNP C C T TCGA-W5-AA2I-01A-32D-A417-09 TCGA-W5-AA2I-10A-01D-A41A-09 g.chr15:43244513C>T c.4969G>A c.(4969-4971)Gca>Aca p.A1657T CHOL 15 43281074 43281074 + Missense_Mutation SNP C C A TCGA-W5-AA2U-01A-11D-A417-09 TCGA-W5-AA2U-10A-01D-A41A-09 g.chr15:43281074C>A c.3940G>T c.(3940-3942)Gat>Tat p.D1314Y CHOL 15 43322177 43322177 + Missense_Mutation SNP G G A TCGA-W5-AA2R-01A-11D-A417-09 TCGA-W5-AA2R-10A-01D-A41A-09 g.chr15:43322177G>A c.2344C>T c.(2344-2346)Cca>Tca p.P782S COAD 15 43244544 43244544 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:43244544G>A c.4938C>T c.(4936-4938)aaC>aaT p.N1646N COAD 15 43252851 43252851 + Silent SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr15:43252851G>A c.4749C>T c.(4747-4749)acC>acT p.T1583T COAD 15 43270128 43270128 + Missense_Mutation SNP T T C TCGA-AA-3538-01A-01W-0831-10 TCGA-AA-3538-10A-01W-0831-10 g.chr15:43270128T>C c.4168A>G c.(4168-4170)Aaa>Gaa p.K1390E COAD 15 43276128 43276128 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:43276128G>T c.4117C>A c.(4117-4119)Ctg>Atg p.L1373M COAD 15 43276155 43276155 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr15:43276155C>T c.4090G>A c.(4090-4092)Gca>Aca p.A1364T COAD 15 43296077 43296077 + Missense_Mutation SNP G G A TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr15:43296077G>A c.3467C>T c.(3466-3468)aCa>aTa p.T1156I COAD 15 43296078 43296078 + Missense_Mutation SNP T T C TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr15:43296078T>C c.3466A>G c.(3466-3468)Aca>Gca p.T1156A COAD 15 43299402 43299402 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:43299402G>A c.3290C>T c.(3289-3291)aCg>aTg p.T1097M COAD 15 43313558 43313558 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:43313558G>A c.2855C>T c.(2854-2856)gCc>gTc p.A952V COAD 15 43317090 43317090 + Silent SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr15:43317090C>T c.2676G>A c.(2674-2676)agG>agA p.R892R COAD 15 43335484 43335484 + Missense_Mutation SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr15:43335484A>G c.1778T>C c.(1777-1779)tTg>tCg p.L593S COAD 15 43335542 43335542 + Missense_Mutation SNP A A G TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr15:43335542A>G c.1720T>C c.(1720-1722)Tgc>Cgc p.C574R COAD 15 43348606 43348606 + Missense_Mutation SNP T T A TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr15:43348606T>A c.1217A>T c.(1216-1218)gAt>gTt p.D406V COAD 15 43367258 43367258 + Silent SNP A A G TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr15:43367258A>G c.447T>C c.(445-447)tgT>tgC p.C149C COAD 15 43374888 43374888 + Missense_Mutation SNP A A G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:43374888A>G c.365T>C c.(364-366)gTa>gCa p.V122A COADREAD 15 43244544 43244544 + Silent SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:43244544G>A c.4938C>T c.(4936-4938)aaC>aaT p.N1646N COADREAD 15 43252851 43252851 + Silent SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr15:43252851G>A c.4749C>T c.(4747-4749)acC>acT p.T1583T COADREAD 15 43270128 43270128 + Missense_Mutation SNP T T C TCGA-AA-3538-01A-01W-0831-10 TCGA-AA-3538-10A-01W-0831-10 g.chr15:43270128T>C c.4168A>G c.(4168-4170)Aaa>Gaa p.K1390E COADREAD 15 43276128 43276128 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr15:43276128G>T c.4117C>A c.(4117-4119)Ctg>Atg p.L1373M COADREAD 15 43276155 43276155 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr15:43276155C>T c.4090G>A c.(4090-4092)Gca>Aca p.A1364T COADREAD 15 43294805 43294805 + Missense_Mutation SNP G G C TCGA-AG-3612-01A-01W-0833-10 TCGA-AG-3612-10A-01W-0833-10 g.chr15:43294805G>C c.3607C>G c.(3607-3609)Ctg>Gtg p.L1203V COADREAD 15 43296077 43296077 + Missense_Mutation SNP G G A TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr15:43296077G>A c.3467C>T c.(3466-3468)aCa>aTa p.T1156I COADREAD 15 43296078 43296078 + Missense_Mutation SNP T T C TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr15:43296078T>C c.3466A>G c.(3466-3468)Aca>Gca p.T1156A COADREAD 15 43299402 43299402 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:43299402G>A c.3290C>T c.(3289-3291)aCg>aTg p.T1097M COADREAD 15 43307955 43307955 + Missense_Mutation SNP G G C TCGA-AF-2689-01A-01W-0831-10 TCGA-AF-2689-10A-01W-0831-10 g.chr15:43307955G>C c.3140C>G c.(3139-3141)aCt>aGt p.T1047S COADREAD 15 43309362 43309362 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:43309362C>T c.2958G>A c.(2956-2958)aaG>aaA p.K986K COADREAD 15 43313558 43313558 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:43313558G>A c.2855C>T c.(2854-2856)gCc>gTc p.A952V COADREAD 15 43317090 43317090 + Silent SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr15:43317090C>T c.2676G>A c.(2674-2676)agG>agA p.R892R COADREAD 15 43335484 43335484 + Missense_Mutation SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr15:43335484A>G c.1778T>C c.(1777-1779)tTg>tCg p.L593S COADREAD 15 43335542 43335542 + Missense_Mutation SNP A A G TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr15:43335542A>G c.1720T>C c.(1720-1722)Tgc>Cgc p.C574R COADREAD 15 43339398 43339398 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:43339398C>A c.1629G>T c.(1627-1629)aaG>aaT p.K543N COADREAD 15 43339471 43339471 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:43339471C>A c.1556G>T c.(1555-1557)cGa>cTa p.R519L COADREAD 15 43340621 43340621 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:43340621C>T c.1508G>A c.(1507-1509)cGa>cAa p.R503Q COADREAD 15 43348606 43348606 + Missense_Mutation SNP T T A TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr15:43348606T>A c.1217A>T c.(1216-1218)gAt>gTt p.D406V COADREAD 15 43367258 43367258 + Silent SNP A A G TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr15:43367258A>G c.447T>C c.(445-447)tgT>tgC p.C149C COADREAD 15 43374888 43374888 + Missense_Mutation SNP A A G TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:43374888A>G c.365T>C c.(364-366)gTa>gCa p.V122A DLBC 15 43256191 43256191 + Missense_Mutation SNP T T C TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr15:43256191T>C c.4642A>G c.(4642-4644)Aca>Gca p.T1548A DLBC 15 43299467 43299467 + Missense_Mutation SNP A A C TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr15:43299467A>C c.3225T>G c.(3223-3225)agT>agG p.S1075R ESCA 15 43244495 43244495 + Missense_Mutation SNP C C T TCGA-L5-A88T-01A-11D-A351-09 TCGA-L5-A88T-11A-11D-A351-09 g.chr15:43244495C>T c.4987G>A c.(4987-4989)Gga>Aga p.G1663R ESCA 15 43252855 43252855 + Frame_Shift_Del DEL T T - TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr15:43252855delT c.4745delA c.(4744-4746)aacfs p.N1582fs ESCA 15 43294822 43294822 + Missense_Mutation SNP C C A TCGA-JY-A6FH-01A-11D-A33E-09 TCGA-JY-A6FH-10A-01D-A33H-09 g.chr15:43294822C>A c.3590G>T c.(3589-3591)tGc>tTc p.C1197F ESCA 15 43307940 43307940 + Missense_Mutation SNP T T G TCGA-L5-A8NS-01A-12D-A37C-09 TCGA-L5-A8NS-11A-11D-A37F-09 g.chr15:43307940T>G c.3155A>C c.(3154-3156)tAt>tCt p.Y1052S ESCA 15 43330047 43330047 + Missense_Mutation SNP G G T TCGA-L7-A6VZ-01A-12D-A33E-09 TCGA-L7-A6VZ-10A-01D-A33H-09 g.chr15:43330047G>T c.1946C>A c.(1945-1947)cCt>cAt p.P649H ESCA 15 43339472 43339472 + Nonsense_Mutation SNP G G A TCGA-R6-A8WG-01A-11D-A37C-09 TCGA-R6-A8WG-10A-01D-A37F-09 g.chr15:43339472G>A c.1555C>T c.(1555-1557)Cga>Tga p.R519* ESCA 15 43348619 43348619 + Missense_Mutation SNP C C T TCGA-V5-AASW-01A-11D-A403-09 TCGA-V5-AASW-10A-01D-A403-09 g.chr15:43348619C>T c.1204G>A c.(1204-1206)Gaa>Aaa p.E402K ESCA 15 43351345 43351345 + Frame_Shift_Del DEL G G - TCGA-JY-A6FA-01A-11D-A33E-09 TCGA-JY-A6FA-10A-01D-A33H-09 g.chr15:43351345delG c.1031delC c.(1030-1032)cctfs p.P344fs ESCA 15 43367261 43367261 + Silent SNP G G A TCGA-VR-A8ER-01A-11D-A36J-09 TCGA-VR-A8ER-10A-01D-A36M-09 g.chr15:43367261G>A c.444C>T c.(442-444)ttC>ttT p.F148F GBM 15 43269028 43269028 + Missense_Mutation SNP T T A TCGA-87-5896-01A-01D-1696-08 TCGA-87-5896-10A-01D-1696-08 g.chr15:43269028T>A c.4256A>T c.(4255-4257)gAt>gTt p.D1419V GBM 15 43317593 43317593 + Missense_Mutation SNP T T C TCGA-06-6390-01A-11D-1696-08 TCGA-06-6390-10A-01D-1696-08 g.chr15:43317593T>C c.2570A>G c.(2569-2571)gAa>gGa p.E857G GBMLGG 15 43269028 43269028 + Missense_Mutation SNP T T A TCGA-87-5896-01A-01D-1696-08 TCGA-87-5896-10A-01D-1696-08 g.chr15:43269028T>A c.4256A>T c.(4255-4257)gAt>gTt p.D1419V GBMLGG 15 43290423 43290423 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43290423G>A c.3700C>T c.(3700-3702)Cgg>Tgg p.R1234W GBMLGG 15 43307949 43307949 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43307949T>C c.3146A>G c.(3145-3147)aAa>aGa p.K1049R GBMLGG 15 43308006 43308006 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43308006C>T c.3089G>A c.(3088-3090)cGc>cAc p.R1030H GBMLGG 15 43317593 43317593 + Missense_Mutation SNP T T C TCGA-06-6390-01A-11D-1696-08 TCGA-06-6390-10A-01D-1696-08 g.chr15:43317593T>C c.2570A>G c.(2569-2571)gAa>gGa p.E857G GBMLGG 15 43330062 43330062 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43330062A>G c.1931T>C c.(1930-1932)gTa>gCa p.V644A GBMLGG 15 43339373 43339373 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43339373A>G c.1654T>C c.(1654-1656)Tgg>Cgg p.W552R GBMLGG 15 43350539 43350539 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43350539C>A c.1182G>T c.(1180-1182)aaG>aaT p.K394N HNSC 15 43252873 43252873 + Missense_Mutation SNP T T G TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chr15:43252873T>G c.4727A>C c.(4726-4728)aAc>aCc p.N1576T HNSC 15 43330042 43330042 + Missense_Mutation SNP G G A TCGA-CV-7416-01A-11D-2078-08 TCGA-CV-7416-10A-01D-2078-08 g.chr15:43330042G>A c.1951C>T c.(1951-1953)Cgt>Tgt p.R651C HNSC 15 43340688 43340688 + Splice_Site SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:43340688A>G c.1441T>C c.(1441-1443)Tat>Cat p.Y481H HNSC 15 43346982 43346982 + Missense_Mutation SNP T T A TCGA-CX-7086-01A-11D-2078-08 TCGA-CX-7086-10D-01D-2078-08 g.chr15:43346982T>A c.1397A>T c.(1396-1398)cAg>cTg p.Q466L HNSC 15 43350570 43350570 + Missense_Mutation SNP T T C TCGA-CV-A6JO-01B-11D-A34J-08 TCGA-CV-A6JO-10A-01D-A34M-08 g.chr15:43350570T>C c.1151A>G c.(1150-1152)tAc>tGc p.Y384C HNSC 15 43350596 43350596 + Silent SNP G G A TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chr15:43350596G>A c.1125C>T c.(1123-1125)ttC>ttT p.F375F HNSC 15 43351984 43351984 + Missense_Mutation SNP C C G TCGA-CQ-5331-01A-02D-1870-08 TCGA-CQ-5331-10A-01D-1870-08 g.chr15:43351984C>G c.901G>C c.(901-903)Gaa>Caa p.E301Q HNSC 15 43360173 43360173 + Missense_Mutation SNP C C T TCGA-CV-7263-01A-11D-2012-08 TCGA-CV-7263-10A-01D-2013-08 g.chr15:43360173C>T c.721G>A c.(721-723)Gtc>Atc p.V241I HNSC 15 43363031 43363031 + Nonsense_Mutation SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr15:43363031C>T c.621G>A c.(619-621)tgG>tgA p.W207* KIPAN 15 43276106 43276106 + Missense_Mutation SNP C C G TCGA-G7-7502-01A-11D-2201-08 TCGA-G7-7502-10A-01D-2201-08 g.chr15:43276106C>G c.4139G>C c.(4138-4140)cGt>cCt p.R1380P KIPAN 15 43281101 43281101 + Nonsense_Mutation SNP C C A TCGA-CJ-4913-01A-01D-1429-08 TCGA-CJ-4913-11A-01D-1429-08 g.chr15:43281101C>A c.3913G>T c.(3913-3915)Gga>Tga p.G1305* KIPAN 15 43299382 43299382 + Missense_Mutation SNP C C T TCGA-G7-6795-01A-11D-1961-08 TCGA-G7-6795-10A-01D-1962-08 g.chr15:43299382C>T c.3310G>A c.(3310-3312)Gaa>Aaa p.E1104K KIPAN 15 43299453 43299453 + Missense_Mutation SNP A A C TCGA-AK-3429-01A-02D-1386-10 TCGA-AK-3429-10A-01D-1251-10 g.chr15:43299453A>C c.3239T>G c.(3238-3240)aTt>aGt p.I1080S KIPAN 15 43299483 43299483 + Splice_Site SNP C C A TCGA-A4-7288-01A-11D-2136-08 TCGA-A4-7288-11A-01D-2136-08 g.chr15:43299483C>A c.e30-1 KIPAN 15 43307885 43307885 + Splice_Site SNP C C A TCGA-B8-4621-01A-01D-1501-10 TCGA-B8-4621-10A-01D-1501-10 g.chr15:43307885C>A c.e29+1 KIPAN 15 43317589 43317589 + Missense_Mutation SNP G G C TCGA-A3-3376-01A-02D-1421-08 TCGA-A3-3376-11A-01D-1421-08 g.chr15:43317589G>C c.2574C>G c.(2572-2574)aaC>aaG p.N858K KIPAN 15 43320014 43320014 + Missense_Mutation SNP T T C TCGA-BP-4176-01A-02D-1366-10 TCGA-BP-4176-11A-01D-1366-10 g.chr15:43320014T>C c.2392A>G c.(2392-2394)Act>Gct p.T798A KIPAN 15 43360146 43360146 + Missense_Mutation SNP C C T TCGA-B0-4818-01A-01D-1501-10 TCGA-B0-4818-11A-01D-1501-10 g.chr15:43360146C>T c.748G>A c.(748-750)Gac>Aac p.D250N KIPAN 15 43367229 43367229 + Missense_Mutation SNP G G C TCGA-AK-3460-01A-02D-1361-10 TCGA-AK-3460-10A-01D-1361-10 g.chr15:43367229G>C c.476C>G c.(475-477)aCt>aGt p.T159S KIPAN 15 43378432 43378432 + Missense_Mutation SNP C C T TCGA-GL-A4EM-01A-11D-A25F-10 TCGA-GL-A4EM-10A-01D-A25F-10 g.chr15:43378432C>T c.88G>A c.(88-90)Gat>Aat p.D30N KIRC 15 43281101 43281101 + Nonsense_Mutation SNP C C A TCGA-CJ-4913-01A-01D-1429-08 TCGA-CJ-4913-11A-01D-1429-08 g.chr15:43281101C>A c.3913G>T c.(3913-3915)Gga>Tga p.G1305* KIRC 15 43299453 43299453 + Missense_Mutation SNP A A C TCGA-AK-3429-01A-02D-1386-10 TCGA-AK-3429-10A-01D-1251-10 g.chr15:43299453A>C c.3239T>G c.(3238-3240)aTt>aGt p.I1080S KIRC 15 43307885 43307885 + Splice_Site SNP C C A TCGA-B8-4621-01A-01D-1501-10 TCGA-B8-4621-10A-01D-1501-10 g.chr15:43307885C>A c.e29+1 KIRC 15 43317589 43317589 + Missense_Mutation SNP G G C TCGA-A3-3376-01A-02D-1421-08 TCGA-A3-3376-11A-01D-1421-08 g.chr15:43317589G>C c.2574C>G c.(2572-2574)aaC>aaG p.N858K KIRC 15 43320014 43320014 + Missense_Mutation SNP T T C TCGA-BP-4176-01A-02D-1366-10 TCGA-BP-4176-11A-01D-1366-10 g.chr15:43320014T>C c.2392A>G c.(2392-2394)Act>Gct p.T798A KIRC 15 43360146 43360146 + Missense_Mutation SNP C C T TCGA-B0-4818-01A-01D-1501-10 TCGA-B0-4818-11A-01D-1501-10 g.chr15:43360146C>T c.748G>A c.(748-750)Gac>Aac p.D250N KIRC 15 43367229 43367229 + Missense_Mutation SNP G G C TCGA-AK-3460-01A-02D-1361-10 TCGA-AK-3460-10A-01D-1361-10 g.chr15:43367229G>C c.476C>G c.(475-477)aCt>aGt p.T159S KIRP 15 43276106 43276106 + Missense_Mutation SNP C C G TCGA-G7-7502-01A-11D-2201-08 TCGA-G7-7502-10A-01D-2201-08 g.chr15:43276106C>G c.4139G>C c.(4138-4140)cGt>cCt p.R1380P KIRP 15 43299382 43299382 + Missense_Mutation SNP C C T TCGA-G7-6795-01A-11D-1961-08 TCGA-G7-6795-10A-01D-1962-08 g.chr15:43299382C>T c.3310G>A c.(3310-3312)Gaa>Aaa p.E1104K KIRP 15 43299483 43299483 + Splice_Site SNP C C A TCGA-A4-7288-01A-11D-2136-08 TCGA-A4-7288-11A-01D-2136-08 g.chr15:43299483C>A c.e30-1 KIRP 15 43378432 43378432 + Missense_Mutation SNP C C T TCGA-GL-A4EM-01A-11D-A25F-10 TCGA-GL-A4EM-10A-01D-A25F-10 g.chr15:43378432C>T c.88G>A c.(88-90)Gat>Aat p.D30N LGG 15 43290423 43290423 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43290423G>A c.3700C>T c.(3700-3702)Cgg>Tgg p.R1234W LGG 15 43307949 43307949 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43307949T>C c.3146A>G c.(3145-3147)aAa>aGa p.K1049R LGG 15 43308006 43308006 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43308006C>T c.3089G>A c.(3088-3090)cGc>cAc p.R1030H LGG 15 43330062 43330062 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43330062A>G c.1931T>C c.(1930-1932)gTa>gCa p.V644A LGG 15 43339373 43339373 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43339373A>G c.1654T>C c.(1654-1656)Tgg>Cgg p.W552R LGG 15 43350539 43350539 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:43350539C>A c.1182G>T c.(1180-1182)aaG>aaT p.K394N LIHC 15 43269020 43269020 + Missense_Mutation SNP C C A TCGA-DD-AADU-01A-11D-A40R-10 TCGA-DD-AADU-10A-01D-A40U-10 g.chr15:43269020C>A c.4264G>T c.(4264-4266)Gtt>Ttt p.V1422F LIHC 15 43314950 43314950 + Missense_Mutation SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr15:43314950T>C c.2789A>G c.(2788-2790)cAa>cGa p.Q930R LIHC 15 43318859 43318859 + Missense_Mutation SNP T T G TCGA-ED-A4XI-01A-11D-A25V-10 TCGA-ED-A4XI-10A-01D-A25V-10 g.chr15:43318859T>G c.2435A>C c.(2434-2436)aAa>aCa p.K812T LIHC 15 43360145 43360145 + Missense_Mutation SNP T T C TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr15:43360145T>C c.749A>G c.(748-750)gAc>gGc p.D250G LIHC 15 43363019 43363019 + Frame_Shift_Del DEL T T - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr15:43363019delT c.633delA c.(631-633)aaafs p.K211fs LIHC 15 43363075 43363075 + Frame_Shift_Del DEL T T - TCGA-BC-A3KG-01A-11D-A20W-10 TCGA-BC-A3KG-10A-01D-A20W-10 g.chr15:43363075delT c.577delA c.(577-579)atafs p.I193fs LUAD 15 43250218 43250218 + Missense_Mutation SNP G G A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr15:43250218G>A c.4828C>T c.(4828-4830)Cat>Tat p.H1610Y LUAD 15 43252861 43252861 + Missense_Mutation SNP T T A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr15:43252861T>A c.4739A>T c.(4738-4740)cAa>cTa p.Q1580L LUAD 15 43258422 43258422 + Missense_Mutation SNP G G A TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chr15:43258422G>A c.4520C>T c.(4519-4521)cCt>cTt p.P1507L LUAD 15 43268937 43268937 + Missense_Mutation SNP C C G TCGA-05-4422-01A-01D-1265-08 TCGA-05-4422-10A-01D-1265-08 g.chr15:43268937C>G c.4347G>C c.(4345-4347)caG>caC p.Q1449H LUAD 15 43270092 43270092 + Silent SNP G G A TCGA-44-8120-01A-11D-2238-08 TCGA-44-8120-10A-01D-2238-08 g.chr15:43270092G>A c.4204C>T c.(4204-4206)Ctg>Ttg p.L1402L LUAD 15 43281045 43281045 + Silent SNP G G A TCGA-50-5941-01A-11D-1753-08 TCGA-50-5941-10A-01D-1753-08 g.chr15:43281045G>A c.3969C>T c.(3967-3969)agC>agT p.S1323S LUAD 15 43282228 43282228 + Splice_Site SNP G G A TCGA-NJ-A55O-01A-11D-A25L-08 TCGA-NJ-A55O-10A-01D-A25L-08 g.chr15:43282228G>A c.3848C>T c.(3847-3849)tCg>tTg p.S1283L LUAD 15 43307940 43307940 + Missense_Mutation SNP T T A TCGA-55-7570-01A-11D-2036-08 TCGA-55-7570-10A-01D-2036-08 g.chr15:43307940T>A c.3155A>T c.(3154-3156)tAt>tTt p.Y1052F LUAD 15 43313527 43313527 + Silent SNP G G C TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chr15:43313527G>C c.2886C>G c.(2884-2886)ctC>ctG p.L962L LUAD 15 43328728 43328728 + Nonsense_Mutation SNP G G A TCGA-95-7948-01A-11D-2184-08 TCGA-95-7948-10A-01D-2184-08 g.chr15:43328728G>A c.2086C>T c.(2086-2088)Cag>Tag p.Q696* LUAD 15 43348568 43348568 + Missense_Mutation SNP C C A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr15:43348568C>A c.1255G>T c.(1255-1257)Gtt>Ttt p.V419F LUAD 15 43360190 43360190 + Missense_Mutation SNP T T A TCGA-86-8359-01A-11D-2323-08 TCGA-86-8359-10A-01D-2323-08 g.chr15:43360190T>A c.704A>T c.(703-705)cAc>cTc p.H235L LUAD 15 43374882 43374882 + Missense_Mutation SNP C C G TCGA-64-1679-01A-21D-2063-08 TCGA-64-1679-10A-01D-2063-08 g.chr15:43374882C>G c.371G>C c.(370-372)tGt>tCt p.C124S LUAD 15 43378282 43378282 + Missense_Mutation SNP C C T TCGA-99-8032-01A-11D-2238-08 TCGA-99-8032-10A-01D-2238-08 g.chr15:43378282C>T c.238G>A c.(238-240)Gga>Aga p.G80R LUAD 15 43378291 43378291 + Missense_Mutation SNP A A T TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr15:43378291A>T c.229T>A c.(229-231)Tac>Aac p.Y77N LUAD 15 43378432 43378432 + Missense_Mutation SNP C C T TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr15:43378432C>T c.88G>A c.(88-90)Gat>Aat p.D30N LUAD 15 43398195 43398195 + Missense_Mutation SNP G G T TCGA-91-6847-01A-11D-1945-08 TCGA-91-6847-11A-01D-1945-08 g.chr15:43398195G>T c.26C>A c.(25-27)aCt>aAt p.T9N LUSC 15 43262764 43262764 + Missense_Mutation SNP G G A TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr15:43262764G>A c.4411C>T c.(4411-4413)Cat>Tat p.H1471Y LUSC 15 43262791 43262791 + Missense_Mutation SNP G G C TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr15:43262791G>C c.4384C>G c.(4384-4386)Cag>Gag p.Q1462E LUSC 15 43281054 43281054 + Silent SNP C C A TCGA-56-6546-01A-11D-1817-08 TCGA-56-6546-10A-01D-1817-08 g.chr15:43281054C>A c.3960G>T c.(3958-3960)ctG>ctT p.L1320L LUSC 15 43313514 43313514 + Nonsense_Mutation SNP G G A TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr15:43313514G>A c.2899C>T c.(2899-2901)Cag>Tag p.Q967* LUSC 15 43314927 43314927 + Missense_Mutation SNP T T C TCGA-22-4595-01A-01D-1267-08 TCGA-22-4595-11A-01D-1267-08 g.chr15:43314927T>C c.2812A>G c.(2812-2814)Aca>Gca p.T938A LUSC 15 43363018 43363018 + Nonsense_Mutation SNP C C A TCGA-18-4721-01A-01D-1441-08 TCGA-18-4721-11A-01D-1441-08 g.chr15:43363018C>A c.634G>T c.(634-636)Gaa>Taa p.E212* LUSC 15 43363118 43363118 + Silent SNP T T A TCGA-39-5036-01A-01D-1441-08 TCGA-39-5036-11A-01D-1441-08 g.chr15:43363118T>A c.534A>T c.(532-534)tcA>tcT p.S178S LUSC 15 43367268 43367268 + Missense_Mutation SNP C C A TCGA-18-3419-01A-01D-0983-08 TCGA-18-3419-11A-01D-0983-08 g.chr15:43367268C>A c.437G>T c.(436-438)gGa>gTa p.G146V PAAD 15 43351939 43351939 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:43351939G>A c.946C>T c.(946-948)Cgt>Tgt p.R316C PRAD 15 43242542 43242542 + Missense_Mutation SNP C C G TCGA-EJ-7784-01A-11D-2114-08 TCGA-EJ-7784-10A-01D-2114-08 g.chr15:43242542C>G c.5026G>C c.(5026-5028)Gtc>Ctc p.V1676L PRAD 15 43262758 43262758 + Missense_Mutation SNP C C T TCGA-EJ-7314-01A-31D-2114-08 TCGA-EJ-7314-10A-01D-2114-08 g.chr15:43262758C>T c.4417G>A c.(4417-4419)Gca>Aca p.A1473T PRAD 15 43276106 43276106 + Missense_Mutation SNP C C T TCGA-CH-5771-01A-21D-1576-08 TCGA-CH-5771-11A-01D-1576-08 g.chr15:43276106C>T c.4139G>A c.(4138-4140)cGt>cAt p.R1380H READ 15 43294805 43294805 + Missense_Mutation SNP G G C TCGA-AG-3612-01A-01W-0833-10 TCGA-AG-3612-10A-01W-0833-10 g.chr15:43294805G>C c.3607C>G c.(3607-3609)Ctg>Gtg p.L1203V READ 15 43307955 43307955 + Missense_Mutation SNP G G C TCGA-AF-2689-01A-01W-0831-10 TCGA-AF-2689-10A-01W-0831-10 g.chr15:43307955G>C c.3140C>G c.(3139-3141)aCt>aGt p.T1047S READ 15 43309362 43309362 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:43309362C>T c.2958G>A c.(2956-2958)aaG>aaA p.K986K READ 15 43339398 43339398 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:43339398C>A c.1629G>T c.(1627-1629)aaG>aaT p.K543N READ 15 43339471 43339471 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:43339471C>A c.1556G>T c.(1555-1557)cGa>cTa p.R519L READ 15 43340621 43340621 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:43340621C>T c.1508G>A c.(1507-1509)cGa>cAa p.R503Q SKCM 15 43237663 43237663 + Missense_Mutation SNP C C A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr15:43237663C>A c.5114G>T c.(5113-5115)gGc>gTc p.G1705V SKCM 15 43237664 43237664 + Missense_Mutation SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr15:43237664C>T c.5113G>A c.(5113-5115)Ggc>Agc p.G1705S SKCM 15 43244481 43244481 + Silent SNP G G A TCGA-EE-A2MN-06A-11D-A197-08 TCGA-EE-A2MN-10A-01D-A199-08 g.chr15:43244481G>A c.5001C>T c.(4999-5001)ttC>ttT p.F1667F SKCM 15 43244516 43244516 + Missense_Mutation SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr15:43244516G>A c.4966C>T c.(4966-4968)Cac>Tac p.H1656Y SKCM 15 43269007 43269007 + Missense_Mutation SNP G G A TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr15:43269007G>A c.4277C>T c.(4276-4278)cCt>cTt p.P1426L SKCM 15 43269030 43269030 + Nonsense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr15:43269030C>T c.4254G>A c.(4252-4254)tgG>tgA p.W1418* SKCM 15 43269040 43269040 + Missense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr15:43269040G>A c.4244C>T c.(4243-4245)tCc>tTc p.S1415F SKCM 15 43299340 43299340 + Missense_Mutation SNP C C T TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr15:43299340C>T c.3352G>A c.(3352-3354)Gcc>Acc p.A1118T SKCM 15 43299342 43299342 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:43299342G>A c.3350C>T c.(3349-3351)tCg>tTg p.S1117L SKCM 15 43314912 43314912 + Missense_Mutation SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr15:43314912G>A c.2827C>T c.(2827-2829)Cat>Tat p.H943Y SKCM 15 43317039 43317039 + Silent SNP C C T TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr15:43317039C>T c.2727G>A c.(2725-2727)ggG>ggA p.G909G SKCM 15 43318759 43318759 + Splice_Site SNP C C T TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr15:43318759C>T c.2535G>A c.(2533-2535)aaG>aaA p.K845K SKCM 15 43328430 43328430 + Frame_Shift_Del DEL A A - TCGA-ER-A1A1-06A-11D-A197-08 TCGA-ER-A1A1-10A-01D-A199-08 g.chr15:43328430delA c.2136delT c.(2134-2136)cttfs p.L712fs SKCM 15 43339380 43339380 + Silent SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr15:43339380G>A c.1647C>T c.(1645-1647)ttC>ttT p.F549F SKCM 15 43339380 43339380 + Silent SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr15:43339380G>A c.1647C>T c.(1645-1647)ttC>ttT p.F549F SKCM 15 43339438 43339438 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr15:43339438G>A c.1589C>T c.(1588-1590)cCt>cTt p.P530L SKCM 15 43340622 43340622 + Nonsense_Mutation SNP G G A TCGA-FS-A1ZR-06A-21D-A197-08 TCGA-FS-A1ZR-10A-01D-A199-08 g.chr15:43340622G>A c.1507C>T c.(1507-1509)Cga>Tga p.R503* SKCM 15 43347094 43347094 + Nonsense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr15:43347094G>A c.1285C>T c.(1285-1287)Cga>Tga p.R429* SKCM 15 43351289 43351289 + Missense_Mutation SNP A A G TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr15:43351289A>G c.1087T>C c.(1087-1089)Tat>Cat p.Y363H SKCM 15 43351929 43351929 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:43351929G>A c.956C>T c.(955-957)tCc>tTc p.S319F SKCM 15 43352305 43352305 + Missense_Mutation SNP C C A TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr15:43352305C>A c.806G>T c.(805-807)cGg>cTg p.R269L SKCM 15 43360109 43360109 + Missense_Mutation SNP G G C TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr15:43360109G>C c.785C>G c.(784-786)gCc>gGc p.A262G SKCM 15 43363004 43363004 + Missense_Mutation SNP T T A TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr15:43363004T>A c.648A>T c.(646-648)gaA>gaT p.E216D SKCM 15 43363063 43363063 + Missense_Mutation SNP C C T TCGA-DA-A1I5-06A-11D-A197-08 TCGA-DA-A1I5-10A-01D-A199-08 g.chr15:43363063C>T c.589G>A c.(589-591)Gtg>Atg p.V197M SKCM 15 43363110 43363110 + Missense_Mutation SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr15:43363110G>A c.542C>T c.(541-543)cCg>cTg p.P181L SKCM 15 43367225 43367225 + Silent SNP G G A TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr15:43367225G>A c.480C>T c.(478-480)ggC>ggT p.G160G

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 15 43258394 43258394 single base substitution G C 3_prime_UTR_variant BLCA-CN 15 43258394 43258394 single base substitution G C missense_variant F1516L 4548C>G BLCA-CN 15 43262760 43262760 single base substitution G A 3_prime_UTR_variant BLCA-CN 15 43262760 43262760 single base substitution G A missense_variant S1472F 4415C>T BLCA-CN 15 43294796 43294796 single base substitution T C 3_prime_UTR_variant BLCA-CN 15 43294796 43294796 single base substitution T C downstream_gene_variant BLCA-CN 15 43294796 43294796 single base substitution T C missense_variant T1206A 3616A>G BLCA-CN 15 43294796 43294796 single base substitution T C upstream_gene_variant BLCA-CN 15 43340619 43340619 single base substitution A G 3_prime_UTR_variant BLCA-CN 15 43340619 43340619 single base substitution A G exon_variant BLCA-CN 15 43340619 43340619 single base substitution A G intron_variant BLCA-CN 15 43340619 43340619 single base substitution A G missense_variant S504P 1510T>C BLCA-US 15 43281096 43281096 single base substitution C G 3_prime_UTR_variant BLCA-US 15 43281096 43281096 single base substitution C G exon_variant BLCA-US 15 43281096 43281096 single base substitution C G missense_variant L1306F 3918G>C BLCA-US 15 43294805 43294805 single base substitution G A 3_prime_UTR_variant BLCA-US 15 43294805 43294805 single base substitution G A downstream_gene_variant BLCA-US 15 43294805 43294805 single base substitution G A synonymous_variant L1203L 3607C>T BLCA-US 15 43294805 43294805 single base substitution G A upstream_gene_variant BLCA-US 15 43294862 43294862 single base substitution G A 3_prime_UTR_variant BLCA-US 15 43294862 43294862 single base substitution G A downstream_gene_variant BLCA-US 15 43294862 43294862 single base substitution G A missense_variant H1184Y 3550C>T BLCA-US 15 43294862 43294862 single base substitution G A upstream_gene_variant BLCA-US 15 43307928 43307928 single base substitution G A 3_prime_UTR_variant BLCA-US 15 43307928 43307928 single base substitution G A exon_variant BLCA-US 15 43307928 43307928 single base substitution G A missense_variant S1056L 3167C>T BLCA-US 15 43339472 43339472 single base substitution G A 3_prime_UTR_variant BLCA-US 15 43339472 43339472 single base substitution G A exon_variant BLCA-US 15 43339472 43339472 single base substitution G A stop_gained R519* 1555C>T BLCA-US 15 43360220 43360220 single base substitution C G exon_variant BLCA-US 15 43360220 43360220 single base substitution C G intron_variant BLCA-US 15 43360220 43360220 single base substitution C G missense_variant R225T 674G>C BOCA-FR 15 43293852 43293852 single base substitution T C downstream_gene_variant BOCA-FR 15 43293852 43293852 single base substitution T C intron_variant BOCA-FR 15 43293852 43293852 single base substitution T C upstream_gene_variant BOCA-FR 15 43364370 43364370 single base substitution C T intron_variant BRCA-EU 15 43230118 43230118 single base substitution C T downstream_gene_variant BRCA-EU 15 43230235 43230235 single base substitution A G downstream_gene_variant BRCA-EU 15 43230486 43230486 single base substitution C G downstream_gene_variant BRCA-EU 15 43230902 43230902 single base substitution C T downstream_gene_variant BRCA-EU 15 43232074 43232074 single base substitution G C downstream_gene_variant BRCA-EU 15 43232352 43232352 single base substitution C T downstream_gene_variant BRCA-EU 15 43232719 43232719 single base substitution T C downstream_gene_variant BRCA-EU 15 43233017 43233017 deletion of <=200bp C - downstream_gene_variant BRCA-EU 15 43233599 43233599 single base substitution C T downstream_gene_variant BRCA-EU 15 43234609 43234609 single base substitution G A downstream_gene_variant BRCA-EU 15 43236257 43236257 single base substitution A G 3_prime_UTR_variant BRCA-EU 15 43236257 43236257 single base substitution A G downstream_gene_variant BRCA-EU 15 43238189 43238189 single base substitution T A intron_variant BRCA-EU 15 43239346 43239346 insertion of <=200bp - A intron_variant BRCA-EU 15 43240756 43240756 single base substitution C G intron_variant BRCA-EU 15 43242370 43242370 single base substitution G A intron_variant BRCA-EU 15 43242446 43242446 deletion of <=200bp A - intron_variant BRCA-EU 15 43243294 43243294 single base substitution G C intron_variant BRCA-EU 15 43243294 43243294 single base substitution G C upstream_gene_variant BRCA-EU 15 43245522 43245522 single base substitution T G intron_variant BRCA-EU 15 43245522 43245522 single base substitution T G upstream_gene_variant BRCA-EU 15 43245631 43245631 single base substitution T C intron_variant BRCA-EU 15 43245631 43245631 single base substitution T C upstream_gene_variant BRCA-EU 15 43246231 43246231 single base substitution C T intron_variant BRCA-EU 15 43246231 43246231 single base substitution C T upstream_gene_variant BRCA-EU 15 43247409 43247409 deletion of <=200bp T - intron_variant BRCA-EU 15 43247409 43247409 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 43247636 43247636 single base substitution C A intron_variant BRCA-EU 15 43247636 43247636 single base substitution C A upstream_gene_variant BRCA-EU 15 43248108 43248108 single base substitution A T intron_variant BRCA-EU 15 43248616 43248616 single base substitution C G intron_variant BRCA-EU 15 43251546 43251546 single base substitution T C intron_variant BRCA-EU 15 43251885 43251885 single base substitution A G intron_variant BRCA-EU 15 43251938 43251938 single base substitution G A intron_variant BRCA-EU 15 43253883 43253883 single base substitution G A intron_variant BRCA-EU 15 43254911 43254911 single base substitution C A intron_variant BRCA-EU 15 43255143 43255143 single base substitution C T intron_variant BRCA-EU 15 43256442 43256442 single base substitution C T intron_variant BRCA-EU 15 43256661 43256661 single base substitution C G intron_variant BRCA-EU 15 43256766 43256766 single base substitution G T intron_variant BRCA-EU 15 43258482 43258482 single base substitution G T missense_variant S1487Y 4460C>A BRCA-EU 15 43258482 43258482 single base substitution G T splice_region_variant BRCA-EU 15 43258496 43258496 single base substitution T C intron_variant BRCA-EU 15 43259561 43259561 single base substitution T G intron_variant BRCA-EU 15 43259938 43259938 single base substitution C A intron_variant BRCA-EU 15 43260503 43260503 single base substitution A C intron_variant BRCA-EU 15 43260692 43260692 single base substitution G A intron_variant BRCA-EU 15 43261552 43261552 single base substitution G A intron_variant BRCA-EU 15 43262129 43262129 single base substitution T C intron_variant BRCA-EU 15 43263065 43263065 single base substitution C T intron_variant BRCA-EU 15 43265224 43265224 single base substitution G C intron_variant BRCA-EU 15 43268090 43268090 deletion of <=200bp T - intron_variant BRCA-EU 15 43268414 43268414 single base substitution T C intron_variant BRCA-EU 15 43270912 43270916 deletion of <=200bp TTTCT - intron_variant BRCA-EU 15 43272192 43272192 single base substitution C T intron_variant BRCA-EU 15 43274117 43274117 single base substitution C G intron_variant BRCA-EU 15 43278236 43278236 single base substitution T C downstream_gene_variant BRCA-EU 15 43278236 43278236 single base substitution T C intron_variant BRCA-EU 15 43278277 43278277 single base substitution A C downstream_gene_variant BRCA-EU 15 43278277 43278277 single base substitution A C intron_variant BRCA-EU 15 43278912 43278912 deletion of <=200bp T - downstream_gene_variant BRCA-EU 15 43278912 43278912 deletion of <=200bp T - intron_variant BRCA-EU 15 43279236 43279236 single base substitution G T downstream_gene_variant BRCA-EU 15 43279236 43279236 single base substitution G T intron_variant BRCA-EU 15 43279298 43279298 single base substitution C A downstream_gene_variant BRCA-EU 15 43279298 43279298 single base substitution C A intron_variant BRCA-EU 15 43280135 43280135 single base substitution T A downstream_gene_variant BRCA-EU 15 43280135 43280135 single base substitution T A intron_variant BRCA-EU 15 43280891 43280891 single base substitution G C exon_variant BRCA-EU 15 43280891 43280891 single base substitution G C intron_variant BRCA-EU 15 43282005 43282005 single base substitution T C intron_variant BRCA-EU 15 43282344 43282344 single base substitution G C intron_variant BRCA-EU 15 43284633 43284633 single base substitution A G intron_variant BRCA-EU 15 43284882 43284882 single base substitution G C intron_variant BRCA-EU 15 43284956 43284956 single base substitution C T intron_variant BRCA-EU 15 43287132 43287132 single base substitution C G intron_variant BRCA-EU 15 43287341 43287341 single base substitution C T intron_variant BRCA-EU 15 43287810 43287810 single base substitution G A intron_variant BRCA-EU 15 43287883 43287883 deletion of <=200bp A - intron_variant BRCA-EU 15 43288378 43288378 single base substitution C G intron_variant BRCA-EU 15 43289963 43289963 single base substitution A G intron_variant BRCA-EU 15 43290715 43290715 single base substitution T A downstream_gene_variant BRCA-EU 15 43290715 43290715 single base substitution T A intron_variant BRCA-EU 15 43290715 43290715 single base substitution T A upstream_gene_variant BRCA-EU 15 43290716 43290716 single base substitution C G downstream_gene_variant BRCA-EU 15 43290716 43290716 single base substitution C G intron_variant BRCA-EU 15 43290716 43290716 single base substitution C G upstream_gene_variant BRCA-EU 15 43296240 43296240 single base substitution G T intron_variant BRCA-EU 15 43298796 43298796 single base substitution G C intron_variant BRCA-EU 15 43299058 43299058 insertion of <=200bp - A intron_variant BRCA-EU 15 43303107 43303107 single base substitution G C downstream_gene_variant BRCA-EU 15 43303107 43303107 single base substitution G C intron_variant BRCA-EU 15 43304344 43304344 single base substitution G C downstream_gene_variant BRCA-EU 15 43304344 43304344 single base substitution G C intron_variant BRCA-EU 15 43304502 43304502 single base substitution A C downstream_gene_variant BRCA-EU 15 43304502 43304502 single base substitution A C intron_variant BRCA-EU 15 43306558 43306558 single base substitution G A downstream_gene_variant BRCA-EU 15 43306558 43306558 single base substitution G A intron_variant BRCA-EU 15 43306787 43306787 single base substitution G T downstream_gene_variant BRCA-EU 15 43306787 43306787 single base substitution G T intron_variant BRCA-EU 15 43307840 43307840 single base substitution A T downstream_gene_variant BRCA-EU 15 43307840 43307840 single base substitution A T intron_variant BRCA-EU 15 43309174 43309174 single base substitution C G downstream_gene_variant BRCA-EU 15 43309174 43309174 single base substitution C G intron_variant BRCA-EU 15 43309174 43309174 single base substitution C G upstream_gene_variant BRCA-EU 15 43309255 43309255 single base substitution A G downstream_gene_variant BRCA-EU 15 43309255 43309255 single base substitution A G intron_variant BRCA-EU 15 43309255 43309255 single base substitution A G upstream_gene_variant BRCA-EU 15 43309513 43309513 deletion of <=200bp A - downstream_gene_variant BRCA-EU 15 43309513 43309513 deletion of <=200bp A - intron_variant BRCA-EU 15 43309513 43309513 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 43311168 43311168 single base substitution G A downstream_gene_variant BRCA-EU 15 43311168 43311168 single base substitution G A intron_variant BRCA-EU 15 43311168 43311168 single base substitution G A upstream_gene_variant BRCA-EU 15 43311459 43311459 single base substitution C T downstream_gene_variant BRCA-EU 15 43311459 43311459 single base substitution C T intron_variant BRCA-EU 15 43311459 43311459 single base substitution C T upstream_gene_variant BRCA-EU 15 43312053 43312053 single base substitution C T downstream_gene_variant BRCA-EU 15 43312053 43312053 single base substitution C T intron_variant BRCA-EU 15 43312053 43312053 single base substitution C T upstream_gene_variant BRCA-EU 15 43313275 43313275 deletion of <=200bp A - downstream_gene_variant BRCA-EU 15 43313275 43313275 deletion of <=200bp A - intron_variant BRCA-EU 15 43315070 43315070 single base substitution A T intron_variant BRCA-EU 15 43315397 43315397 single base substitution T C intron_variant BRCA-EU 15 43316873 43316873 deletion of <=200bp A - intron_variant BRCA-EU 15 43317141 43317141 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 43317141 43317141 single base substitution G A exon_variant BRCA-EU 15 43317141 43317141 single base substitution G A synonymous_variant F64F 192C>T BRCA-EU 15 43317141 43317141 single base substitution G A synonymous_variant F875F 2625C>T BRCA-EU 15 43317851 43317851 single base substitution C A 3_prime_UTR_variant BRCA-EU 15 43317851 43317851 single base substitution C A intron_variant BRCA-EU 15 43322288 43322288 deletion of <=200bp A - intron_variant BRCA-EU 15 43322288 43322288 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 43322806 43322806 deletion of <=200bp A - intron_variant BRCA-EU 15 43322806 43322806 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 43323011 43323011 single base substitution G C intron_variant BRCA-EU 15 43323011 43323011 single base substitution G C upstream_gene_variant BRCA-EU 15 43324210 43324210 single base substitution C T intron_variant BRCA-EU 15 43324210 43324210 single base substitution C T upstream_gene_variant BRCA-EU 15 43324857 43324857 single base substitution T C intron_variant BRCA-EU 15 43324857 43324857 single base substitution T C upstream_gene_variant BRCA-EU 15 43326752 43326752 single base substitution G C intron_variant BRCA-EU 15 43327441 43327441 single base substitution A C intron_variant BRCA-EU 15 43327972 43327972 single base substitution A G intron_variant BRCA-EU 15 43328301 43328301 single base substitution A G intron_variant BRCA-EU 15 43330475 43330475 single base substitution T A downstream_gene_variant BRCA-EU 15 43330475 43330475 single base substitution T A intron_variant BRCA-EU 15 43330475 43330475 single base substitution T A upstream_gene_variant BRCA-EU 15 43331037 43331037 single base substitution G A downstream_gene_variant BRCA-EU 15 43331037 43331037 single base substitution G A intron_variant BRCA-EU 15 43331037 43331037 single base substitution G A upstream_gene_variant BRCA-EU 15 43331212 43331212 single base substitution T G downstream_gene_variant BRCA-EU 15 43331212 43331212 single base substitution T G intron_variant BRCA-EU 15 43331212 43331212 single base substitution T G upstream_gene_variant BRCA-EU 15 43333463 43333463 single base substitution A G downstream_gene_variant BRCA-EU 15 43333463 43333463 single base substitution A G intron_variant BRCA-EU 15 43333463 43333463 single base substitution A G upstream_gene_variant BRCA-EU 15 43333624 43333624 single base substitution C G downstream_gene_variant BRCA-EU 15 43333624 43333624 single base substitution C G intron_variant BRCA-EU 15 43333624 43333624 single base substitution C G upstream_gene_variant BRCA-EU 15 43335908 43335908 single base substitution G A intron_variant BRCA-EU 15 43336325 43336325 single base substitution G C intron_variant BRCA-EU 15 43341078 43341078 single base substitution C T intron_variant BRCA-EU 15 43341316 43341316 single base substitution A G intron_variant BRCA-EU 15 43342855 43342855 single base substitution G A intron_variant BRCA-EU 15 43343128 43343128 single base substitution C T intron_variant BRCA-EU 15 43343147 43343147 insertion of <=200bp - A intron_variant BRCA-EU 15 43344933 43344933 single base substitution G C intron_variant BRCA-EU 15 43346697 43346697 single base substitution G C intron_variant BRCA-EU 15 43348782 43348782 single base substitution T C intron_variant BRCA-EU 15 43348995 43348995 single base substitution C T intron_variant BRCA-EU 15 43351239 43351239 single base substitution T C intron_variant BRCA-EU 15 43353583 43353583 single base substitution G C intron_variant BRCA-EU 15 43353583 43353583 single base substitution G C upstream_gene_variant BRCA-EU 15 43354320 43354320 single base substitution G A intron_variant BRCA-EU 15 43354320 43354320 single base substitution G A upstream_gene_variant BRCA-EU 15 43354321 43354321 single base substitution C T intron_variant BRCA-EU 15 43354321 43354321 single base substitution C T upstream_gene_variant BRCA-EU 15 43354440 43354440 single base substitution G A intron_variant BRCA-EU 15 43354440 43354440 single base substitution G A upstream_gene_variant BRCA-EU 15 43357010 43357010 single base substitution C T intron_variant BRCA-EU 15 43357920 43357920 single base substitution A G intron_variant BRCA-EU 15 43358457 43358457 single base substitution C T intron_variant BRCA-EU 15 43359424 43359424 insertion of <=200bp - T intron_variant BRCA-EU 15 43360613 43360613 single base substitution G C intron_variant BRCA-EU 15 43360761 43360761 single base substitution C T intron_variant BRCA-EU 15 43362060 43362060 single base substitution G T intron_variant BRCA-EU 15 43362103 43362103 single base substitution C A intron_variant BRCA-EU 15 43363415 43363415 single base substitution C T intron_variant BRCA-EU 15 43363833 43363833 deletion of <=200bp A - intron_variant BRCA-EU 15 43365133 43365133 single base substitution G A intron_variant BRCA-EU 15 43369481 43369481 single base substitution G C intron_variant BRCA-EU 15 43371474 43371474 single base substitution G T downstream_gene_variant BRCA-EU 15 43371474 43371474 single base substitution G T intron_variant BRCA-EU 15 43371576 43371576 single base substitution C T downstream_gene_variant BRCA-EU 15 43371576 43371576 single base substitution C T intron_variant BRCA-EU 15 43373516 43373516 single base substitution G A downstream_gene_variant BRCA-EU 15 43373516 43373516 single base substitution G A intron_variant BRCA-EU 15 43375589 43375589 single base substitution G C intron_variant BRCA-EU 15 43375603 43375603 single base substitution C G intron_variant BRCA-EU 15 43378450 43378450 single base substitution G C intron_variant BRCA-EU 15 43378652 43378652 single base substitution A G intron_variant BRCA-EU 15 43379321 43379321 single base substitution G A intron_variant BRCA-EU 15 43379572 43379572 single base substitution C T intron_variant BRCA-EU 15 43379608 43379608 single base substitution A T intron_variant BRCA-EU 15 43379944 43379944 deletion of <=200bp T - intron_variant BRCA-EU 15 43380807 43380807 single base substitution C T intron_variant BRCA-EU 15 43382476 43382476 single base substitution G C intron_variant BRCA-EU 15 43383777 43383777 single base substitution T A intron_variant BRCA-EU 15 43385085 43385085 single base substitution C T intron_variant BRCA-EU 15 43385834 43385834 single base substitution G C intron_variant BRCA-EU 15 43387371 43387371 single base substitution A T intron_variant BRCA-EU 15 43390998 43390998 single base substitution G A intron_variant BRCA-EU 15 43391306 43391306 single base substitution G C intron_variant BRCA-EU 15 43391508 43391508 single base substitution C G intron_variant BRCA-EU 15 43393031 43393031 deletion of <=200bp A - intron_variant BRCA-EU 15 43393521 43393521 single base substitution G A intron_variant BRCA-EU 15 43395301 43395301 single base substitution A C intron_variant BRCA-EU 15 43396549 43396549 single base substitution C T intron_variant BRCA-EU 15 43398720 43398720 single base substitution A G upstream_gene_variant BRCA-EU 15 43399480 43399480 single base substitution A G upstream_gene_variant BRCA-EU 15 43399735 43399735 single base substitution C T upstream_gene_variant BRCA-EU 15 43399798 43399798 single base substitution A T upstream_gene_variant BRCA-EU 15 43400483 43400483 single base substitution G A upstream_gene_variant BRCA-EU 15 43401576 43401576 single base substitution G C upstream_gene_variant BRCA-EU 15 43402099 43402099 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 43402099 43402099 single base substitution A T upstream_gene_variant BRCA-EU 15 43402183 43402183 single base substitution G A upstream_gene_variant BRCA-EU 15 43402224 43402224 single base substitution G A upstream_gene_variant BRCA-FR 15 43230486 43230486 single base substitution C G downstream_gene_variant BRCA-FR 15 43233322 43233322 single base substitution C G downstream_gene_variant BRCA-FR 15 43233599 43233599 single base substitution C G downstream_gene_variant BRCA-FR 15 43246639 43246639 single base substitution T C intron_variant BRCA-FR 15 43246639 43246639 single base substitution T C upstream_gene_variant BRCA-FR 15 43255143 43255143 single base substitution C T intron_variant BRCA-FR 15 43256766 43256766 single base substitution G T intron_variant BRCA-FR 15 43259938 43259938 single base substitution C A intron_variant BRCA-FR 15 43290383 43290383 single base substitution T C 3_prime_UTR_variant BRCA-FR 15 43290383 43290383 single base substitution T C exon_variant BRCA-FR 15 43290383 43290383 single base substitution T C missense_variant N1247S 3740A>G BRCA-FR 15 43304344 43304344 single base substitution G C downstream_gene_variant BRCA-FR 15 43304344 43304344 single base substitution G C intron_variant BRCA-FR 15 43307600 43307600 single base substitution G A downstream_gene_variant BRCA-FR 15 43307600 43307600 single base substitution G A intron_variant BRCA-FR 15 43317141 43317141 single base substitution G A 3_prime_UTR_variant BRCA-FR 15 43317141 43317141 single base substitution G A exon_variant BRCA-FR 15 43317141 43317141 single base substitution G A synonymous_variant F64F 192C>T BRCA-FR 15 43317141 43317141 single base substitution G A synonymous_variant F875F 2625C>T BRCA-FR 15 43330475 43330475 single base substitution T A downstream_gene_variant BRCA-FR 15 43330475 43330475 single base substitution T A intron_variant BRCA-FR 15 43330475 43330475 single base substitution T A upstream_gene_variant BRCA-FR 15 43333024 43333024 single base substitution C A downstream_gene_variant BRCA-FR 15 43333024 43333024 single base substitution C A intron_variant BRCA-FR 15 43333024 43333024 single base substitution C A upstream_gene_variant BRCA-FR 15 43341078 43341078 single base substitution C T intron_variant BRCA-FR 15 43346697 43346697 single base substitution G C intron_variant BRCA-FR 15 43353583 43353583 single base substitution G C intron_variant BRCA-FR 15 43353583 43353583 single base substitution G C upstream_gene_variant BRCA-FR 15 43358457 43358457 single base substitution C T intron_variant BRCA-FR 15 43365133 43365133 single base substitution G A intron_variant BRCA-FR 15 43375589 43375589 single base substitution G C intron_variant BRCA-FR 15 43379608 43379608 single base substitution A T intron_variant BRCA-FR 15 43389645 43389645 single base substitution C T intron_variant BRCA-FR 15 43391664 43391664 single base substitution G A intron_variant BRCA-FR 15 43393521 43393521 single base substitution G A intron_variant BRCA-FR 15 43401576 43401576 single base substitution G C upstream_gene_variant BRCA-FR 15 43401795 43401795 single base substitution A G upstream_gene_variant BRCA-UK 15 43253646 43253646 single base substitution G C intron_variant BRCA-UK 15 43255127 43255127 single base substitution G C intron_variant BRCA-UK 15 43255132 43255132 single base substitution G A intron_variant BRCA-UK 15 43256174 43256174 single base substitution G A 3_prime_UTR_variant BRCA-UK 15 43256174 43256174 single base substitution G A synonymous_variant L1553L 4659C>T BRCA-UK 15 43258482 43258482 single base substitution G T missense_variant S1487Y 4460C>A BRCA-UK 15 43258482 43258482 single base substitution G T splice_region_variant BRCA-UK 15 43274425 43274425 single base substitution G A intron_variant BRCA-UK 15 43278277 43278277 single base substitution A C downstream_gene_variant BRCA-UK 15 43278277 43278277 single base substitution A C intron_variant BRCA-UK 15 43293283 43293283 single base substitution C G downstream_gene_variant BRCA-UK 15 43293283 43293283 single base substitution C G intron_variant BRCA-UK 15 43293283 43293283 single base substitution C G upstream_gene_variant BRCA-UK 15 43375603 43375603 single base substitution C G intron_variant BRCA-UK 15 43382181 43382181 single base substitution G A intron_variant BRCA-UK 15 43401685 43401685 single base substitution G T upstream_gene_variant BRCA-US 15 43244537 43244537 single base substitution C G 3_prime_UTR_variant BRCA-US 15 43244537 43244537 single base substitution C G missense_variant E1649Q 4945G>C BRCA-US 15 43244537 43244537 single base substitution C G upstream_gene_variant BRCA-US 15 43269025 43269025 single base substitution T A 3_prime_UTR_variant BRCA-US 15 43269025 43269025 single base substitution T A missense_variant D1420V 4259A>T BRCA-US 15 43269026 43269026 single base substitution C T 3_prime_UTR_variant BRCA-US 15 43269026 43269026 single base substitution C T missense_variant D1420N 4258G>A BRCA-US 15 43281144 43281144 single base substitution G C 3_prime_UTR_variant BRCA-US 15 43281144 43281144 single base substitution G C exon_variant BRCA-US 15 43281144 43281144 single base substitution G C missense_variant I1290M 3870C>G BRCA-US 15 43282235 43282235 single base substitution C T 3_prime_UTR_variant BRCA-US 15 43282235 43282235 single base substitution C T exon_variant BRCA-US 15 43282235 43282235 single base substitution C T missense_variant E1281K 3841G>A BRCA-US 15 43347026 43347026 single base substitution C A exon_variant BRCA-US 15 43347026 43347026 single base substitution C A intron_variant BRCA-US 15 43347026 43347026 single base substitution C A missense_variant E451D 1353G>T BRCA-US 15 43348619 43348619 single base substitution C A 3_prime_UTR_variant BRCA-US 15 43348619 43348619 single base substitution C A exon_variant BRCA-US 15 43348619 43348619 single base substitution C A intron_variant BRCA-US 15 43348619 43348619 single base substitution C A stop_gained E402* 1204G>T BRCA-US 15 43360113 43360113 single base substitution T C exon_variant BRCA-US 15 43360113 43360113 single base substitution T C intron_variant BRCA-US 15 43360113 43360113 single base substitution T C missense_variant T261A 781A>G BRCA-US 15 43363018 43363018 single base substitution C T exon_variant BRCA-US 15 43363018 43363018 single base substitution C T intron_variant BRCA-US 15 43363018 43363018 single base substitution C T missense_variant E212K 634G>A BRCA-US 15 43363024 43363024 single base substitution C T exon_variant BRCA-US 15 43363024 43363024 single base substitution C T intron_variant BRCA-US 15 43363024 43363024 single base substitution C T missense_variant E210K 628G>A BTCA-JP 15 43268863 43268863 single base substitution G A intron_variant BTCA-JP 15 43290485 43290485 single base substitution T C downstream_gene_variant BTCA-JP 15 43290485 43290485 single base substitution T C intron_variant BTCA-JP 15 43290485 43290485 single base substitution T C upstream_gene_variant BTCA-JP 15 43294860 43294864 deletion of <=200bp ATGAA - 3_prime_UTR_variant BTCA-JP 15 43294860 43294864 deletion of <=200bp ATGAA - downstream_gene_variant BTCA-JP 15 43294860 43294864 deletion of <=200bp ATGAA - frameshift_variant IH1183 BTCA-JP 15 43294860 43294864 deletion of <=200bp ATGAA - upstream_gene_variant BTCA-JP 15 43295027 43295027 single base substitution C T downstream_gene_variant BTCA-JP 15 43295027 43295027 single base substitution C T intron_variant BTCA-JP 15 43295027 43295027 single base substitution C T upstream_gene_variant BTCA-JP 15 43315062 43315062 single base substitution T G intron_variant BTCA-JP 15 43320154 43320154 single base substitution C T intron_variant BTCA-JP 15 43320154 43320154 single base substitution C T upstream_gene_variant BTCA-JP 15 43330451 43330451 single base substitution G A downstream_gene_variant BTCA-JP 15 43330451 43330451 single base substitution G A intron_variant BTCA-JP 15 43330451 43330451 single base substitution G A upstream_gene_variant BTCA-JP 15 43330514 43330514 single base substitution C T downstream_gene_variant BTCA-JP 15 43330514 43330514 single base substitution C T intron_variant BTCA-JP 15 43330514 43330514 single base substitution C T upstream_gene_variant BTCA-JP 15 43335395 43335395 deletion of <=200bp G - downstream_gene_variant BTCA-JP 15 43335395 43335395 deletion of <=200bp G - intron_variant BTCA-JP 15 43348653 43348653 single base substitution A C intron_variant BTCA-JP 15 43398108 43398108 deletion of <=200bp A - intron_variant BTCA-JP 15 43398237 43398257 deletion of <=200bp GCCTGCAGTTGCCGACCCCCG - 5_prime_UTR_variant BTCA-JP 15 43398237 43398257 deletion of <=200bp GCCTGCAGTTGCCGACCCCCG - exon_variant CESC-US 15 43270092 43270092 single base substitution G A 3_prime_UTR_variant CESC-US 15 43270092 43270092 single base substitution G A synonymous_variant L1402L 4204C>T CESC-US 15 43329982 43329982 single base substitution G C exon_variant CESC-US 15 43329982 43329982 single base substitution G C missense_variant L671V 2011C>G CESC-US 15 43330009 43330009 single base substitution C T exon_variant CESC-US 15 43330009 43330009 single base substitution C T missense_variant E662K 1984G>A CESC-US 15 43335480 43335480 single base substitution T C 3_prime_UTR_variant CESC-US 15 43335480 43335480 single base substitution T C downstream_gene_variant CESC-US 15 43335480 43335480 single base substitution T C exon_variant CESC-US 15 43335480 43335480 single base substitution T C synonymous_variant E594E 1782A>G CLLE-ES 15 43286548 43286548 single base substitution T C intron_variant CLLE-ES 15 43296592 43296592 single base substitution C G intron_variant CLLE-ES 15 43370078 43370078 single base substitution T A downstream_gene_variant CLLE-ES 15 43370078 43370078 single base substitution T A intron_variant COAD-US 15 43250280 43250280 single base substitution C A 3_prime_UTR_variant COAD-US 15 43250280 43250280 single base substitution C A missense_variant R1589I 4766G>T COAD-US 15 43276128 43276128 single base substitution G T 3_prime_UTR_variant COAD-US 15 43276128 43276128 single base substitution G T downstream_gene_variant COAD-US 15 43276128 43276128 single base substitution G T missense_variant L1373M 4117C>A COAD-US 15 43299402 43299402 single base substitution G A 3_prime_UTR_variant COAD-US 15 43299402 43299402 single base substitution G A exon_variant COAD-US 15 43299402 43299402 single base substitution G A missense_variant T1097M 3290C>T COAD-US 15 43335484 43335484 single base substitution A G 3_prime_UTR_variant COAD-US 15 43335484 43335484 single base substitution A G downstream_gene_variant COAD-US 15 43335484 43335484 single base substitution A G exon_variant COAD-US 15 43335484 43335484 single base substitution A G missense_variant L593S 1778T>C COAD-US 15 43351981 43351981 single base substitution C T exon_variant COAD-US 15 43351981 43351981 single base substitution C T intron_variant COAD-US 15 43351981 43351981 single base substitution C T missense_variant V302I 904G>A COAD-US 15 43367258 43367258 single base substitution A G 3_prime_UTR_variant COAD-US 15 43367258 43367258 single base substitution A G exon_variant COAD-US 15 43367258 43367258 single base substitution A G synonymous_variant C149C 447T>C COAD-US 15 43374888 43374888 single base substitution A G 3_prime_UTR_variant COAD-US 15 43374888 43374888 single base substitution A G downstream_gene_variant COAD-US 15 43374888 43374888 single base substitution A G exon_variant COAD-US 15 43374888 43374888 single base substitution A G missense_variant V122A 365T>C COCA-CN 15 43237631 43237631 single base substitution G A 3_prime_UTR_variant COCA-CN 15 43237631 43237631 single base substitution G A exon_variant COCA-CN 15 43237631 43237631 single base substitution G A missense_variant R1716W 5146C>T COCA-CN 15 43250092 43250092 single base substitution C A intron_variant COCA-CN 15 43256121 43256121 single base substitution T C intron_variant COCA-CN 15 43256250 43256250 single base substitution G T intron_variant COCA-CN 15 43258436 43258436 single base substitution C A 3_prime_UTR_variant COCA-CN 15 43258436 43258436 single base substitution C A missense_variant K1502N 4506G>T COCA-CN 15 43262594 43262594 single base substitution G T intron_variant COCA-CN 15 43276144 43276144 single base substitution A G 3_prime_UTR_variant COCA-CN 15 43276144 43276144 single base substitution A G downstream_gene_variant COCA-CN 15 43276144 43276144 single base substitution A G synonymous_variant I1367I 4101T>C COCA-CN 15 43280908 43280908 single base substitution C T exon_variant COCA-CN 15 43280908 43280908 single base substitution C T intron_variant COCA-CN 15 43280947 43280947 single base substitution G T exon_variant COCA-CN 15 43280947 43280947 single base substitution G T intron_variant COCA-CN 15 43282205 43282205 single base substitution C A intron_variant COCA-CN 15 43297338 43297338 single base substitution G A intron_variant COCA-CN 15 43307840 43307840 single base substitution A T downstream_gene_variant COCA-CN 15 43307840 43307840 single base substitution A T intron_variant COCA-CN 15 43307941 43307941 single base substitution A G 3_prime_UTR_variant COCA-CN 15 43307941 43307941 single base substitution A G exon_variant COCA-CN 15 43307941 43307941 single base substitution A G missense_variant Y1052H 3154T>C COCA-CN 15 43307945 43307945 single base substitution G A 3_prime_UTR_variant COCA-CN 15 43307945 43307945 single base substitution G A exon_variant COCA-CN 15 43307945 43307945 single base substitution G A synonymous_variant L1050L 3150C>T COCA-CN 15 43317640 43317640 single base substitution C A 3_prime_UTR_variant COCA-CN 15 43317640 43317640 single base substitution C A intron_variant COCA-CN 15 43318727 43318727 single base substitution G C 3_prime_UTR_variant COCA-CN 15 43318727 43318727 single base substitution G C intron_variant COCA-CN 15 43322155 43322155 single base substitution T G exon_variant COCA-CN 15 43322155 43322155 single base substitution T G missense_variant N789T 2366A>C COCA-CN 15 43322155 43322155 single base substitution T G upstream_gene_variant COCA-CN 15 43339310 43339310 single base substitution T G intron_variant COCA-CN 15 43340494 43340494 single base substitution C A intron_variant COCA-CN 15 43351437 43351437 single base substitution C A intron_variant COCA-CN 15 43367127 43367127 single base substitution C A intron_variant COCA-CN 15 43367167 43367167 single base substitution G T intron_variant COCA-CN 15 43378146 43378146 single base substitution T A intron_variant COCA-CN 15 43378177 43378177 single base substitution C T intron_variant COCA-CN 15 43378177 43378177 single base substitution C T splice_region_variant COCA-CN 15 43378328 43378328 single base substitution T G 3_prime_UTR_variant COCA-CN 15 43378328 43378328 single base substitution T G exon_variant COCA-CN 15 43378328 43378328 single base substitution T G intron_variant COCA-CN 15 43378328 43378328 single base substitution T G missense_variant E64D 192A>C COCA-CN 15 43384485 43384485 single base substitution T G intron_variant EOPC-DE 15 43230797 43230797 single base substitution C T downstream_gene_variant EOPC-DE 15 43381426 43381426 single base substitution T C intron_variant EOPC-DE 15 43395151 43395151 single base substitution G T intron_variant ESAD-UK 15 43244051 43244051 single base substitution C T intron_variant ESAD-UK 15 43244051 43244051 single base substitution C T upstream_gene_variant ESAD-UK 15 43244201 43244201 single base substitution A C intron_variant ESAD-UK 15 43244201 43244201 single base substitution A C upstream_gene_variant ESAD-UK 15 43244955 43244955 single base substitution G T intron_variant ESAD-UK 15 43244955 43244955 single base substitution G T upstream_gene_variant ESAD-UK 15 43245407 43245407 single base substitution G T intron_variant ESAD-UK 15 43245407 43245407 single base substitution G T upstream_gene_variant ESAD-UK 15 43246346 43246346 single base substitution G A intron_variant ESAD-UK 15 43246346 43246346 single base substitution G A upstream_gene_variant ESAD-UK 15 43247409 43247409 deletion of <=200bp T - intron_variant ESAD-UK 15 43247409 43247409 deletion of <=200bp T - upstream_gene_variant ESAD-UK 15 43248665 43248665 single base substitution G A intron_variant ESAD-UK 15 43248744 43248744 single base substitution G A intron_variant ESAD-UK 15 43250074 43250074 single base substitution C A intron_variant ESAD-UK 15 43259791 43259791 single base substitution G C intron_variant ESAD-UK 15 43264115 43264115 single base substitution G C intron_variant ESAD-UK 15 43268090 43268090 single base substitution T A intron_variant ESAD-UK 15 43273443 43273443 single base substitution A T intron_variant ESAD-UK 15 43273727 43273727 single base substitution G A intron_variant ESAD-UK 15 43274569 43274569 single base substitution G A intron_variant ESAD-UK 15 43275480 43275480 single base substitution G A intron_variant ESAD-UK 15 43276322 43276322 single base substitution C T downstream_gene_variant ESAD-UK 15 43276322 43276322 single base substitution C T intron_variant ESAD-UK 15 43276904 43276904 single base substitution G A downstream_gene_variant ESAD-UK 15 43276904 43276904 single base substitution G A intron_variant ESAD-UK 15 43279327 43279327 single base substitution C T downstream_gene_variant ESAD-UK 15 43279327 43279327 single base substitution C T intron_variant ESAD-UK 15 43285060 43285060 single base substitution G A intron_variant ESAD-UK 15 43285913 43285913 single base substitution G A intron_variant ESAD-UK 15 43286961 43286961 single base substitution G A intron_variant ESAD-UK 15 43288238 43288238 single base substitution A C intron_variant ESAD-UK 15 43288798 43288798 single base substitution A T intron_variant ESAD-UK 15 43289163 43289163 single base substitution C G intron_variant ESAD-UK 15 43290304 43290304 single base substitution T A intron_variant ESAD-UK 15 43290649 43290649 single base substitution C T downstream_gene_variant ESAD-UK 15 43290649 43290649 single base substitution C T intron_variant ESAD-UK 15 43290649 43290649 single base substitution C T upstream_gene_variant ESAD-UK 15 43290905 43290905 single base substitution A G downstream_gene_variant ESAD-UK 15 43290905 43290905 single base substitution A G intron_variant ESAD-UK 15 43290905 43290905 single base substitution A G upstream_gene_variant ESAD-UK 15 43290911 43290911 single base substitution A T downstream_gene_variant ESAD-UK 15 43290911 43290911 single base substitution A T intron_variant ESAD-UK 15 43290911 43290911 single base substitution A T upstream_gene_variant ESAD-UK 15 43293939 43293939 single base substitution C A downstream_gene_variant ESAD-UK 15 43293939 43293939 single base substitution C A intron_variant ESAD-UK 15 43293939 43293939 single base substitution C A upstream_gene_variant ESAD-UK 15 43295183 43295183 single base substitution T C downstream_gene_variant ESAD-UK 15 43295183 43295183 single base substitution T C intron_variant ESAD-UK 15 43295183 43295183 single base substitution T C upstream_gene_variant ESAD-UK 15 43295189 43295189 single base substitution C A downstream_gene_variant ESAD-UK 15 43295189 43295189 single base substitution C A intron_variant ESAD-UK 15 43295189 43295189 single base substitution C A upstream_gene_variant ESAD-UK 15 43296948 43296948 single base substitution C G intron_variant ESAD-UK 15 43297846 43297846 single base substitution A T intron_variant ESAD-UK 15 43298632 43298632 single base substitution G T intron_variant ESAD-UK 15 43300187 43300187 single base substitution C G intron_variant ESAD-UK 15 43305601 43305601 single base substitution T A downstream_gene_variant ESAD-UK 15 43305601 43305601 single base substitution T A intron_variant ESAD-UK 15 43305602 43305602 single base substitution C A downstream_gene_variant ESAD-UK 15 43305602 43305602 single base substitution C A intron_variant ESAD-UK 15 43305702 43305702 single base substitution C G downstream_gene_variant ESAD-UK 15 43305702 43305702 single base substitution C G intron_variant ESAD-UK 15 43307610 43307610 single base substitution G A downstream_gene_variant ESAD-UK 15 43307610 43307610 single base substitution G A intron_variant ESAD-UK 15 43312804 43312804 single base substitution C T downstream_gene_variant ESAD-UK 15 43312804 43312804 single base substitution C T intron_variant ESAD-UK 15 43312804 43312804 single base substitution C T upstream_gene_variant ESAD-UK 15 43315042 43315042 single base substitution A G intron_variant ESAD-UK 15 43319541 43319541 single base substitution C T intron_variant ESAD-UK 15 43319541 43319541 single base substitution C T upstream_gene_variant ESAD-UK 15 43320676 43320676 single base substitution G A intron_variant ESAD-UK 15 43320676 43320676 single base substitution G A upstream_gene_variant ESAD-UK 15 43321176 43321176 single base substitution G A intron_variant ESAD-UK 15 43321176 43321176 single base substitution G A upstream_gene_variant ESAD-UK 15 43322627 43322627 single base substitution G A intron_variant ESAD-UK 15 43322627 43322627 single base substitution G A upstream_gene_variant ESAD-UK 15 43324147 43324147 single base substitution G A intron_variant ESAD-UK 15 43324147 43324147 single base substitution G A upstream_gene_variant ESAD-UK 15 43325478 43325478 single base substitution A C intron_variant ESAD-UK 15 43326086 43326086 single base substitution G A intron_variant ESAD-UK 15 43327479 43327479 deletion of <=200bp T - intron_variant ESAD-UK 15 43327522 43327522 insertion of <=200bp - A intron_variant ESAD-UK 15 43330672 43330672 single base substitution A T downstream_gene_variant ESAD-UK 15 43330672 43330672 single base substitution A T intron_variant ESAD-UK 15 43330672 43330672 single base substitution A T upstream_gene_variant ESAD-UK 15 43331114 43331114 deletion of <=200bp T - downstream_gene_variant ESAD-UK 15 43331114 43331114 deletion of <=200bp T - intron_variant ESAD-UK 15 43331114 43331114 deletion of <=200bp T - upstream_gene_variant ESAD-UK 15 43332518 43332518 single base substitution G T downstream_gene_variant ESAD-UK 15 43332518 43332518 single base substitution G T intron_variant ESAD-UK 15 43332518 43332518 single base substitution G T upstream_gene_variant ESAD-UK 15 43335456 43335456 single base substitution C A 3_prime_UTR_variant ESAD-UK 15 43335456 43335456 single base substitution C A downstream_gene_variant ESAD-UK 15 43335456 43335456 single base substitution C A exon_variant ESAD-UK 15 43335456 43335456 single base substitution C A missense_variant E602D 1806G>T ESAD-UK 15 43336761 43336761 single base substitution C A intron_variant ESAD-UK 15 43337079 43337079 single base substitution C T intron_variant ESAD-UK 15 43339018 43339018 single base substitution A T intron_variant ESAD-UK 15 43341806 43341806 deletion of <=200bp T - intron_variant ESAD-UK 15 43342249 43342249 single base substitution G A intron_variant ESAD-UK 15 43342487 43342487 single base substitution G A intron_variant ESAD-UK 15 43343512 43343512 single base substitution C T intron_variant ESAD-UK 15 43345801 43345801 deletion of <=200bp T - intron_variant ESAD-UK 15 43351433 43351433 single base substitution T G intron_variant ESAD-UK 15 43352867 43352867 single base substitution G A intron_variant ESAD-UK 15 43352867 43352867 single base substitution G A upstream_gene_variant ESAD-UK 15 43358021 43358021 deletion of <=200bp T - intron_variant ESAD-UK 15 43358298 43358298 single base substitution G A intron_variant ESAD-UK 15 43360447 43360447 single base substitution C T intron_variant ESAD-UK 15 43360780 43360780 single base substitution C T intron_variant ESAD-UK 15 43362181 43362181 single base substitution T A intron_variant ESAD-UK 15 43370166 43370166 insertion of <=200bp - A downstream_gene_variant ESAD-UK 15 43370166 43370166 insertion of <=200bp - A intron_variant ESAD-UK 15 43371335 43371335 single base substitution G A downstream_gene_variant ESAD-UK 15 43371335 43371335 single base substitution G A intron_variant ESAD-UK 15 43376887 43376887 single base substitution G A intron_variant ESAD-UK 15 43377517 43377517 single base substitution C T intron_variant ESAD-UK 15 43378601 43378601 single base substitution G A intron_variant ESAD-UK 15 43379344 43379344 single base substitution C T intron_variant ESAD-UK 15 43379360 43379360 single base substitution T G intron_variant ESAD-UK 15 43379475 43379475 single base substitution C T intron_variant ESAD-UK 15 43380819 43380819 single base substitution A T intron_variant ESAD-UK 15 43386106 43386106 single base substitution T A intron_variant ESAD-UK 15 43386186 43386186 single base substitution G A intron_variant ESAD-UK 15 43386541 43386541 single base substitution C T intron_variant ESAD-UK 15 43387563 43387563 single base substitution G T intron_variant ESAD-UK 15 43387708 43387708 single base substitution G A intron_variant ESAD-UK 15 43388458 43388458 single base substitution G C intron_variant ESAD-UK 15 43388592 43388592 single base substitution T C intron_variant ESAD-UK 15 43391528 43391528 single base substitution A C intron_variant ESAD-UK 15 43391530 43391530 single base substitution C A intron_variant ESAD-UK 15 43392409 43392409 single base substitution A C intron_variant ESAD-UK 15 43393158 43393158 single base substitution T C intron_variant ESAD-UK 15 43393892 43393892 single base substitution C A intron_variant ESAD-UK 15 43396790 43396790 single base substitution T C intron_variant ESAD-UK 15 43398398 43398398 single base substitution G A upstream_gene_variant ESAD-UK 15 43398817 43398817 single base substitution T A upstream_gene_variant ESAD-UK 15 43399383 43399383 single base substitution A G upstream_gene_variant ESAD-UK 15 43400458 43400458 single base substitution G C upstream_gene_variant ESAD-UK 15 43401120 43401120 single base substitution G T upstream_gene_variant ESAD-UK 15 43401699 43401699 single base substitution G T upstream_gene_variant ESAD-UK 15 43402060 43402060 single base substitution T G upstream_gene_variant ESAD-UK 15 43402107 43402107 single base substitution G T upstream_gene_variant ESAD-UK 15 43402550 43402550 single base substitution A G upstream_gene_variant ESAD-UK 15 43402646 43402646 single base substitution C T upstream_gene_variant ESCA-CN 15 43314945 43314945 single base substitution C T 3_prime_UTR_variant ESCA-CN 15 43314945 43314945 single base substitution C T exon_variant ESCA-CN 15 43314945 43314945 single base substitution C T missense_variant A121T 361G>A ESCA-CN 15 43314945 43314945 single base substitution C T missense_variant A932T 2794G>A ESCA-CN 15 43348570 43348570 single base substitution G C 3_prime_UTR_variant ESCA-CN 15 43348570 43348570 single base substitution G C exon_variant ESCA-CN 15 43348570 43348570 single base substitution G C intron_variant ESCA-CN 15 43348570 43348570 single base substitution G C stop_gained S418* 1253C>G GBM-US 15 43269028 43269028 single base substitution T A 3_prime_UTR_variant GBM-US 15 43269028 43269028 single base substitution T A missense_variant D1419V 4256A>T KIRC-US 15 43281101 43281101 single base substitution C A 3_prime_UTR_variant KIRC-US 15 43281101 43281101 single base substitution C A exon_variant KIRC-US 15 43281101 43281101 single base substitution C A stop_gained G1305* 3913G>T KIRC-US 15 43299453 43299453 single base substitution A C 3_prime_UTR_variant KIRC-US 15 43299453 43299453 single base substitution A C exon_variant KIRC-US 15 43299453 43299453 single base substitution A C missense_variant I1080S 3239T>G KIRC-US 15 43307885 43307885 single base substitution C A exon_variant KIRC-US 15 43307885 43307885 single base substitution C A splice_donor_variant KIRC-US 15 43317589 43317589 single base substitution G C 3_prime_UTR_variant KIRC-US 15 43317589 43317589 single base substitution G C exon_variant KIRC-US 15 43317589 43317589 single base substitution G C missense_variant N47K 141C>G KIRC-US 15 43317589 43317589 single base substitution G C missense_variant N858K 2574C>G KIRC-US 15 43320014 43320014 single base substitution T C exon_variant KIRC-US 15 43320014 43320014 single base substitution T C intron_variant KIRC-US 15 43320014 43320014 single base substitution T C missense_variant T798A 2392A>G KIRC-US 15 43320014 43320014 single base substitution T C upstream_gene_variant KIRC-US 15 43360146 43360146 single base substitution C T exon_variant KIRC-US 15 43360146 43360146 single base substitution C T intron_variant KIRC-US 15 43360146 43360146 single base substitution C T missense_variant D250N 748G>A KIRC-US 15 43367229 43367229 single base substitution G C 3_prime_UTR_variant KIRC-US 15 43367229 43367229 single base substitution G C exon_variant KIRC-US 15 43367229 43367229 single base substitution G C missense_variant T159S 476C>G KIRP-US 15 43299382 43299382 single base substitution C T 3_prime_UTR_variant KIRP-US 15 43299382 43299382 single base substitution C T exon_variant KIRP-US 15 43299382 43299382 single base substitution C T missense_variant E1104K 3310G>A KIRP-US 15 43299483 43299483 single base substitution C A splice_acceptor_variant KIRP-US 15 43378432 43378432 single base substitution C T 3_prime_UTR_variant KIRP-US 15 43378432 43378432 single base substitution C T exon_variant KIRP-US 15 43378432 43378432 single base substitution C T intron_variant KIRP-US 15 43378432 43378432 single base substitution C T missense_variant D30N 88G>A LAML-KR 15 43254150 43254150 single base substitution A G intron_variant LAML-KR 15 43351803 43351803 single base substitution G A intron_variant LAML-KR 15 43368510 43368510 single base substitution C T intron_variant LICA-CN 15 43244556 43244556 single base substitution C A 3_prime_UTR_variant LICA-CN 15 43244556 43244556 single base substitution C A missense_variant Q1642H 4926G>T LICA-CN 15 43244556 43244556 single base substitution C A upstream_gene_variant LICA-CN 15 43244570 43244570 single base substitution T A 3_prime_UTR_variant LICA-CN 15 43244570 43244570 single base substitution T A missense_variant N1638Y 4912A>T LICA-CN 15 43244570 43244570 single base substitution T A upstream_gene_variant LICA-CN 15 43299309 43299309 single base substitution T A 3_prime_UTR_variant LICA-CN 15 43299309 43299309 single base substitution T A exon_variant LICA-CN 15 43299309 43299309 single base substitution T A missense_variant Q1128L 3383A>T LICA-CN 15 43340679 43340679 single base substitution T C 3_prime_UTR_variant LICA-CN 15 43340679 43340679 single base substitution T C exon_variant LICA-CN 15 43340679 43340679 single base substitution T C intron_variant LICA-CN 15 43340679 43340679 single base substitution T C missense_variant I484V 1450A>G LICA-FR 15 43241393 43241393 single base substitution C T intron_variant LICA-FR 15 43257663 43257663 deletion of <=200bp T - intron_variant LICA-FR 15 43271091 43271092 deletion of <=200bp TT - intron_variant LICA-FR 15 43277907 43277907 single base substitution C T downstream_gene_variant LICA-FR 15 43277907 43277907 single base substitution C T intron_variant LICA-FR 15 43293798 43293798 single base substitution T C downstream_gene_variant LICA-FR 15 43293798 43293798 single base substitution T C intron_variant LICA-FR 15 43293798 43293798 single base substitution T C upstream_gene_variant LICA-FR 15 43296093 43296093 single base substitution C T 3_prime_UTR_variant LICA-FR 15 43296093 43296093 single base substitution C T exon_variant LICA-FR 15 43296093 43296093 single base substitution C T missense_variant A1151T 3451G>A LICA-FR 15 43297992 43297992 single base substitution C T intron_variant LICA-FR 15 43298304 43298304 single base substitution G A intron_variant LICA-FR 15 43330408 43330408 single base substitution C T exon_variant LICA-FR 15 43330408 43330408 single base substitution C T synonymous_variant R624R 1872G>A LICA-FR 15 43330408 43330408 single base substitution C T upstream_gene_variant LICA-FR 15 43330622 43330622 single base substitution C A downstream_gene_variant LICA-FR 15 43330622 43330622 single base substitution C A intron_variant LICA-FR 15 43330622 43330622 single base substitution C A upstream_gene_variant LICA-FR 15 43335883 43335883 single base substitution G T intron_variant LICA-FR 15 43351381 43351381 single base substitution C T exon_variant LICA-FR 15 43351381 43351381 single base substitution C T intron_variant LICA-FR 15 43351381 43351381 single base substitution C T missense_variant R332K 995G>A LICA-FR 15 43368252 43368252 single base substitution C G intron_variant LIHC-US 15 43314950 43314950 single base substitution T C 3_prime_UTR_variant LIHC-US 15 43314950 43314950 single base substitution T C exon_variant LIHC-US 15 43314950 43314950 single base substitution T C missense_variant Q119R 356A>G LIHC-US 15 43314950 43314950 single base substitution T C missense_variant Q930R 2789A>G LIHC-US 15 43318859 43318859 single base substitution T G missense_variant E794D 2382A>C LIHC-US 15 43318859 43318859 single base substitution T G missense_variant K1T 2A>C LIHC-US 15 43318859 43318859 single base substitution T G missense_variant K812T 2435A>C LIHC-US 15 43318859 43318859 single base substitution T G splice_region_variant LINC-JP 15 43236190 43236190 single base substitution T C 3_prime_UTR_variant LINC-JP 15 43236190 43236190 single base substitution T C downstream_gene_variant LINC-JP 15 43236192 43236192 single base substitution T A 3_prime_UTR_variant LINC-JP 15 43236192 43236192 single base substitution T A downstream_gene_variant LINC-JP 15 43236673 43236673 single base substitution A T 3_prime_UTR_variant LINC-JP 15 43236673 43236673 single base substitution A T downstream_gene_variant LINC-JP 15 43238962 43238962 single base substitution T C intron_variant LINC-JP 15 43259612 43259612 insertion of <=200bp - T intron_variant LINC-JP 15 43264787 43264787 single base substitution T A intron_variant LINC-JP 15 43271894 43271894 single base substitution A C intron_variant LINC-JP 15 43273148 43273148 single base substitution C T intron_variant LINC-JP 15 43296231 43296231 single base substitution T A intron_variant LINC-JP 15 43302525 43302525 insertion of <=200bp - A intron_variant LINC-JP 15 43315842 43315842 single base substitution G A intron_variant LINC-JP 15 43332450 43332450 single base substitution A T downstream_gene_variant LINC-JP 15 43332450 43332450 single base substitution A T intron_variant LINC-JP 15 43332450 43332450 single base substitution A T upstream_gene_variant LINC-JP 15 43334521 43334521 single base substitution T A downstream_gene_variant LINC-JP 15 43334521 43334521 single base substitution T A intron_variant LINC-JP 15 43334521 43334521 single base substitution T A upstream_gene_variant LINC-JP 15 43336680 43336680 single base substitution A G intron_variant LINC-JP 15 43339329 43339329 single base substitution G A intron_variant LINC-JP 15 43346656 43346656 single base substitution G C intron_variant LINC-JP 15 43347106 43347106 single base substitution T A intron_variant LINC-JP 15 43364658 43364658 single base substitution C T intron_variant LINC-JP 15 43371885 43371885 single base substitution C A downstream_gene_variant LINC-JP 15 43371885 43371885 single base substitution C A intron_variant LINC-JP 15 43387090 43387090 single base substitution T C intron_variant LINC-JP 15 43395928 43395928 single base substitution T C intron_variant LINC-JP 15 43396389 43396389 single base substitution A G intron_variant LINC-JP 15 43398407 43398407 deletion of <=200bp T - upstream_gene_variant LIRI-JP 15 43232674 43232674 single base substitution C T downstream_gene_variant LIRI-JP 15 43234348 43234348 single base substitution C T downstream_gene_variant LIRI-JP 15 43236503 43236503 single base substitution T G 3_prime_UTR_variant LIRI-JP 15 43236503 43236503 single base substitution T G downstream_gene_variant LIRI-JP 15 43236710 43236710 single base substitution G A 3_prime_UTR_variant LIRI-JP 15 43236710 43236710 single base substitution G A downstream_gene_variant LIRI-JP 15 43239400 43239400 single base substitution T A intron_variant LIRI-JP 15 43240639 43240639 single base substitution T C intron_variant LIRI-JP 15 43241710 43241711 deletion of <=200bp CT - intron_variant LIRI-JP 15 43246217 43246217 single base substitution A G intron_variant LIRI-JP 15 43246217 43246217 single base substitution A G upstream_gene_variant LIRI-JP 15 43247318 43247318 single base substitution C T intron_variant LIRI-JP 15 43247318 43247318 single base substitution C T upstream_gene_variant LIRI-JP 15 43249324 43249324 single base substitution T A intron_variant LIRI-JP 15 43250141 43250141 single base substitution T C intron_variant LIRI-JP 15 43255455 43255455 single base substitution A T intron_variant LIRI-JP 15 43257612 43257612 single base substitution T C intron_variant LIRI-JP 15 43262703 43262703 single base substitution T C intron_variant LIRI-JP 15 43263658 43263658 single base substitution T C intron_variant LIRI-JP 15 43264133 43264133 single base substitution T C intron_variant LIRI-JP 15 43264173 43264173 single base substitution C T intron_variant LIRI-JP 15 43264728 43264728 single base substitution G C intron_variant LIRI-JP 15 43270907 43270907 single base substitution G C intron_variant LIRI-JP 15 43273179 43273179 deletion of <=200bp T - intron_variant LIRI-JP 15 43273375 43273375 single base substitution A C intron_variant LIRI-JP 15 43274874 43274874 single base substitution G C intron_variant LIRI-JP 15 43276376 43276376 single base substitution C A downstream_gene_variant LIRI-JP 15 43276376 43276376 single base substitution C A intron_variant LIRI-JP 15 43276926 43276926 single base substitution C A downstream_gene_variant LIRI-JP 15 43276926 43276926 single base substitution C A intron_variant LIRI-JP 15 43283411 43283411 single base substitution C T intron_variant LIRI-JP 15 43283466 43283466 single base substitution G A intron_variant LIRI-JP 15 43285466 43285466 single base substitution T A intron_variant LIRI-JP 15 43289354 43289354 single base substitution G A intron_variant LIRI-JP 15 43290429 43290429 single base substitution G C 3_prime_UTR_variant LIRI-JP 15 43290429 43290429 single base substitution G C missense_variant L1232V 3694C>G LIRI-JP 15 43290429 43290429 single base substitution G C upstream_gene_variant LIRI-JP 15 43294058 43294058 single base substitution A C downstream_gene_variant LIRI-JP 15 43294058 43294058 single base substitution A C intron_variant LIRI-JP 15 43294058 43294058 single base substitution A C upstream_gene_variant LIRI-JP 15 43296411 43296411 single base substitution T C intron_variant LIRI-JP 15 43301723 43301723 single base substitution A C intron_variant LIRI-JP 15 43302480 43302480 single base substitution T A intron_variant LIRI-JP 15 43303371 43303371 single base substitution C A downstream_gene_variant LIRI-JP 15 43303371 43303371 single base substitution C A intron_variant LIRI-JP 15 43305313 43305313 single base substitution G C downstream_gene_variant LIRI-JP 15 43305313 43305313 single base substitution G C intron_variant LIRI-JP 15 43305550 43305550 single base substitution C T downstream_gene_variant LIRI-JP 15 43305550 43305550 single base substitution C T intron_variant LIRI-JP 15 43310484 43310484 single base substitution C A downstream_gene_variant LIRI-JP 15 43310484 43310484 single base substitution C A intron_variant LIRI-JP 15 43310484 43310484 single base substitution C A upstream_gene_variant LIRI-JP 15 43312608 43312608 single base substitution T C downstream_gene_variant LIRI-JP 15 43312608 43312608 single base substitution T C intron_variant LIRI-JP 15 43312608 43312608 single base substitution T C upstream_gene_variant LIRI-JP 15 43312925 43312925 single base substitution T C downstream_gene_variant LIRI-JP 15 43312925 43312925 single base substitution T C intron_variant LIRI-JP 15 43312925 43312925 single base substitution T C upstream_gene_variant LIRI-JP 15 43313098 43313098 single base substitution C T downstream_gene_variant LIRI-JP 15 43313098 43313098 single base substitution C T intron_variant LIRI-JP 15 43313992 43313992 single base substitution T A intron_variant LIRI-JP 15 43315597 43315597 single base substitution C G intron_variant LIRI-JP 15 43316850 43316850 single base substitution G T intron_variant LIRI-JP 15 43317556 43317556 single base substitution C A intron_variant LIRI-JP 15 43318390 43318390 single base substitution A G 3_prime_UTR_variant LIRI-JP 15 43318390 43318390 single base substitution A G intron_variant LIRI-JP 15 43318405 43318405 single base substitution G T 3_prime_UTR_variant LIRI-JP 15 43318405 43318405 single base substitution G T intron_variant LIRI-JP 15 43321631 43321631 single base substitution G A intron_variant LIRI-JP 15 43321631 43321631 single base substitution G A upstream_gene_variant LIRI-JP 15 43322067 43322067 single base substitution T C intron_variant LIRI-JP 15 43322067 43322067 single base substitution T C upstream_gene_variant LIRI-JP 15 43325076 43325076 single base substitution C T intron_variant LIRI-JP 15 43327016 43327016 single base substitution C T intron_variant LIRI-JP 15 43328292 43328292 single base substitution C T intron_variant LIRI-JP 15 43328847 43328847 single base substitution T C intron_variant LIRI-JP 15 43330137 43330137 single base substitution A C intron_variant LIRI-JP 15 43330137 43330137 single base substitution A C upstream_gene_variant LIRI-JP 15 43330562 43330562 single base substitution T C downstream_gene_variant LIRI-JP 15 43330562 43330562 single base substitution T C intron_variant LIRI-JP 15 43330562 43330562 single base substitution T C upstream_gene_variant LIRI-JP 15 43331507 43331507 single base substitution A G downstream_gene_variant LIRI-JP 15 43331507 43331507 single base substitution A G intron_variant LIRI-JP 15 43331507 43331507 single base substitution A G upstream_gene_variant LIRI-JP 15 43333676 43333676 single base substitution C T downstream_gene_variant LIRI-JP 15 43333676 43333676 single base substitution C T intron_variant LIRI-JP 15 43333676 43333676 single base substitution C T upstream_gene_variant LIRI-JP 15 43336780 43336780 insertion of <=200bp - T intron_variant LIRI-JP 15 43339536 43339536 single base substitution T C intron_variant LIRI-JP 15 43340517 43340517 single base substitution C A intron_variant LIRI-JP 15 43343896 43343896 single base substitution T G intron_variant LIRI-JP 15 43345486 43345486 single base substitution T C intron_variant LIRI-JP 15 43346569 43346569 single base substitution T C intron_variant LIRI-JP 15 43349163 43349163 single base substitution G T intron_variant LIRI-JP 15 43349709 43349709 single base substitution T C intron_variant LIRI-JP 15 43351009 43351009 single base substitution T C intron_variant LIRI-JP 15 43351387 43351387 single base substitution T A exon_variant LIRI-JP 15 43351387 43351387 single base substitution T A intron_variant LIRI-JP 15 43351387 43351387 single base substitution T A missense_variant D330V 989A>T LIRI-JP 15 43352029 43352029 single base substitution A T intron_variant LIRI-JP 15 43352029 43352029 single base substitution A T splice_region_variant LIRI-JP 15 43352029 43352029 single base substitution A T upstream_gene_variant LIRI-JP 15 43352169 43352169 single base substitution T C intron_variant LIRI-JP 15 43352169 43352169 single base substitution T C upstream_gene_variant LIRI-JP 15 43353842 43353842 single base substitution T C intron_variant LIRI-JP 15 43353842 43353842 single base substitution T C upstream_gene_variant LIRI-JP 15 43355292 43355292 single base substitution T C intron_variant LIRI-JP 15 43355292 43355292 single base substitution T C upstream_gene_variant LIRI-JP 15 43362890 43362890 single base substitution T C intron_variant LIRI-JP 15 43363223 43363223 single base substitution T C intron_variant LIRI-JP 15 43370938 43370938 single base substitution G T downstream_gene_variant LIRI-JP 15 43370938 43370938 single base substitution G T intron_variant LIRI-JP 15 43371607 43371607 single base substitution A T downstream_gene_variant LIRI-JP 15 43371607 43371607 single base substitution A T intron_variant LIRI-JP 15 43374072 43374072 single base substitution G A downstream_gene_variant LIRI-JP 15 43374072 43374072 single base substitution G A intron_variant LIRI-JP 15 43375070 43375070 single base substitution G C intron_variant LIRI-JP 15 43375080 43375080 single base substitution C T intron_variant LIRI-JP 15 43378386 43378386 single base substitution T A 3_prime_UTR_variant LIRI-JP 15 43378386 43378386 single base substitution T A exon_variant LIRI-JP 15 43378386 43378386 single base substitution T A intron_variant LIRI-JP 15 43378386 43378386 single base substitution T A missense_variant Q45L 134A>T LIRI-JP 15 43378830 43378830 single base substitution T C intron_variant LIRI-JP 15 43379495 43379495 single base substitution C T intron_variant LIRI-JP 15 43380734 43380734 single base substitution T C intron_variant LIRI-JP 15 43382110 43382110 single base substitution G C intron_variant LIRI-JP 15 43385180 43385180 single base substitution A T intron_variant LIRI-JP 15 43387307 43387307 single base substitution T C intron_variant LIRI-JP 15 43389807 43389807 single base substitution C A intron_variant LIRI-JP 15 43393499 43393499 single base substitution G T intron_variant LIRI-JP 15 43396313 43396313 single base substitution T C intron_variant LIRI-JP 15 43399218 43399218 single base substitution A G upstream_gene_variant LIRI-JP 15 43400691 43400691 single base substitution G A upstream_gene_variant LIRI-JP 15 43400904 43400904 single base substitution A G upstream_gene_variant LIRI-JP 15 43401271 43401271 single base substitution A G upstream_gene_variant LIRI-JP 15 43401776 43401776 single base substitution G T upstream_gene_variant LIRI-JP 15 43402087 43402087 single base substitution A G upstream_gene_variant LUSC-CN 15 43322088 43322088 single base substitution G C intron_variant LUSC-CN 15 43322088 43322088 single base substitution G C upstream_gene_variant LUSC-KR 15 43233192 43233192 single base substitution A T downstream_gene_variant LUSC-KR 15 43233220 43233220 single base substitution G T downstream_gene_variant LUSC-KR 15 43240213 43240213 single base substitution C T intron_variant LUSC-KR 15 43241474 43241474 single base substitution T C intron_variant LUSC-KR 15 43243710 43243710 single base substitution C A intron_variant LUSC-KR 15 43243710 43243710 single base substitution C A upstream_gene_variant LUSC-KR 15 43246855 43246855 single base substitution T A intron_variant LUSC-KR 15 43246855 43246855 single base substitution T A upstream_gene_variant LUSC-KR 15 43266674 43266674 single base substitution T C intron_variant LUSC-KR 15 43269902 43269902 single base substitution A T intron_variant LUSC-KR 15 43279451 43279451 single base substitution G A downstream_gene_variant LUSC-KR 15 43279451 43279451 single base substitution G A intron_variant LUSC-KR 15 43284668 43284668 single base substitution T G intron_variant LUSC-KR 15 43287623 43287623 single base substitution C A intron_variant LUSC-KR 15 43287636 43287636 single base substitution T A intron_variant LUSC-KR 15 43288008 43288008 single base substitution G A intron_variant LUSC-KR 15 43289646 43289646 single base substitution T A intron_variant LUSC-KR 15 43291154 43291154 single base substitution G T downstream_gene_variant LUSC-KR 15 43291154 43291154 single base substitution G T intron_variant LUSC-KR 15 43291154 43291154 single base substitution G T upstream_gene_variant LUSC-KR 15 43293738 43293738 single base substitution C T downstream_gene_variant LUSC-KR 15 43293738 43293738 single base substitution C T intron_variant LUSC-KR 15 43293738 43293738 single base substitution C T upstream_gene_variant LUSC-KR 15 43294328 43294328 single base substitution T C downstream_gene_variant LUSC-KR 15 43294328 43294328 single base substitution T C intron_variant LUSC-KR 15 43294328 43294328 single base substitution T C upstream_gene_variant LUSC-KR 15 43298115 43298115 single base substitution C A intron_variant LUSC-KR 15 43298189 43298189 single base substitution C T intron_variant LUSC-KR 15 43298243 43298243 single base substitution C G intron_variant LUSC-KR 15 43298258 43298258 single base substitution G C intron_variant LUSC-KR 15 43298994 43298994 single base substitution C G intron_variant LUSC-KR 15 43305229 43305229 single base substitution G A downstream_gene_variant LUSC-KR 15 43305229 43305229 single base substitution G A intron_variant LUSC-KR 15 43307516 43307516 single base substitution G T downstream_gene_variant LUSC-KR 15 43307516 43307516 single base substitution G T intron_variant LUSC-KR 15 43307600 43307600 single base substitution G A downstream_gene_variant LUSC-KR 15 43307600 43307600 single base substitution G A intron_variant LUSC-KR 15 43307719 43307719 single base substitution C T downstream_gene_variant LUSC-KR 15 43307719 43307719 single base substitution C T intron_variant LUSC-KR 15 43311817 43311817 single base substitution G T downstream_gene_variant LUSC-KR 15 43311817 43311817 single base substitution G T intron_variant LUSC-KR 15 43311817 43311817 single base substitution G T upstream_gene_variant LUSC-KR 15 43335311 43335311 single base substitution T C downstream_gene_variant LUSC-KR 15 43335311 43335311 single base substitution T C intron_variant LUSC-KR 15 43351803 43351803 single base substitution G A intron_variant LUSC-KR 15 43354263 43354263 single base substitution T C intron_variant LUSC-KR 15 43354263 43354263 single base substitution T C upstream_gene_variant LUSC-KR 15 43360286 43360286 single base substitution G A intron_variant LUSC-KR 15 43368191 43368191 single base substitution G C intron_variant LUSC-KR 15 43368389 43368389 single base substitution G A intron_variant LUSC-KR 15 43368998 43368998 single base substitution A G intron_variant LUSC-KR 15 43369025 43369025 single base substitution G T intron_variant LUSC-KR 15 43370676 43370676 single base substitution A T downstream_gene_variant LUSC-KR 15 43370676 43370676 single base substitution A T intron_variant LUSC-KR 15 43371809 43371809 single base substitution C G downstream_gene_variant LUSC-KR 15 43371809 43371809 single base substitution C G intron_variant LUSC-KR 15 43372265 43372265 single base substitution G A downstream_gene_variant LUSC-KR 15 43372265 43372265 single base substitution G A intron_variant LUSC-KR 15 43372543 43372543 single base substitution T G downstream_gene_variant LUSC-KR 15 43372543 43372543 single base substitution T G intron_variant LUSC-KR 15 43372932 43372932 single base substitution C A downstream_gene_variant LUSC-KR 15 43372932 43372932 single base substitution C A intron_variant LUSC-KR 15 43374321 43374321 single base substitution G A downstream_gene_variant LUSC-KR 15 43374321 43374321 single base substitution G A intron_variant LUSC-KR 15 43383382 43383382 single base substitution C A intron_variant LUSC-KR 15 43383496 43383496 single base substitution C A intron_variant LUSC-KR 15 43393134 43393134 single base substitution A C intron_variant LUSC-KR 15 43397042 43397042 single base substitution A G intron_variant LUSC-US 15 43262764 43262764 single base substitution G A 3_prime_UTR_variant LUSC-US 15 43262764 43262764 single base substitution G A missense_variant H1471Y 4411C>T LUSC-US 15 43262791 43262791 single base substitution G C 3_prime_UTR_variant LUSC-US 15 43262791 43262791 single base substitution G C missense_variant Q1462E 4384C>G LUSC-US 15 43281054 43281054 single base substitution C A 3_prime_UTR_variant LUSC-US 15 43281054 43281054 single base substitution C A exon_variant LUSC-US 15 43281054 43281054 single base substitution C A synonymous_variant L1320L 3960G>T LUSC-US 15 43313514 43313514 single base substitution G A 3_prime_UTR_variant LUSC-US 15 43313514 43313514 single base substitution G A exon_variant LUSC-US 15 43313514 43313514 single base substitution G A stop_gained Q156* 466C>T LUSC-US 15 43313514 43313514 single base substitution G A stop_gained Q967* 2899C>T LUSC-US 15 43314927 43314927 single base substitution T C 3_prime_UTR_variant LUSC-US 15 43314927 43314927 single base substitution T C exon_variant LUSC-US 15 43314927 43314927 single base substitution T C missense_variant T127A 379A>G LUSC-US 15 43314927 43314927 single base substitution T C missense_variant T938A 2812A>G LUSC-US 15 43363018 43363018 single base substitution C A exon_variant LUSC-US 15 43363018 43363018 single base substitution C A intron_variant LUSC-US 15 43363018 43363018 single base substitution C A stop_gained E212* 634G>T LUSC-US 15 43363118 43363118 single base substitution T A 3_prime_UTR_variant LUSC-US 15 43363118 43363118 single base substitution T A exon_variant LUSC-US 15 43363118 43363118 single base substitution T A synonymous_variant S178S 534A>T LUSC-US 15 43367268 43367268 single base substitution C A 3_prime_UTR_variant LUSC-US 15 43367268 43367268 single base substitution C A exon_variant LUSC-US 15 43367268 43367268 single base substitution C A missense_variant G146V 437G>T MALY-DE 15 43235805 43235805 single base substitution T C 3_prime_UTR_variant MALY-DE 15 43235805 43235805 single base substitution T C downstream_gene_variant MALY-DE 15 43238447 43238447 single base substitution A T intron_variant MALY-DE 15 43238448 43238448 single base substitution G A intron_variant MALY-DE 15 43245708 43245708 single base substitution C T intron_variant MALY-DE 15 43245708 43245708 single base substitution C T upstream_gene_variant MALY-DE 15 43264333 43264334 deletion of <=200bp AC - intron_variant MALY-DE 15 43272788 43272791 deletion of <=200bp ATCC - intron_variant MALY-DE 15 43277653 43277653 single base substitution C T downstream_gene_variant MALY-DE 15 43277653 43277653 single base substitution C T intron_variant MALY-DE 15 43281655 43281655 single base substitution C A intron_variant MALY-DE 15 43288803 43288803 single base substitution A C intron_variant MALY-DE 15 43297772 43297786 deletion of <=200bp ACCCCGTCTGGGAGG - intron_variant MALY-DE 15 43299811 43299811 single base substitution T A intron_variant MALY-DE 15 43311353 43311353 single base substitution G A downstream_gene_variant MALY-DE 15 43311353 43311353 single base substitution G A intron_variant MALY-DE 15 43311353 43311353 single base substitution G A upstream_gene_variant MALY-DE 15 43311957 43311957 single base substitution T G downstream_gene_variant MALY-DE 15 43311957 43311957 single base substitution T G intron_variant MALY-DE 15 43311957 43311957 single base substitution T G upstream_gene_variant MALY-DE 15 43321754 43321754 single base substitution G A intron_variant MALY-DE 15 43321754 43321754 single base substitution G A upstream_gene_variant MALY-DE 15 43321975 43321975 single base substitution C T intron_variant MALY-DE 15 43321975 43321975 single base substitution C T upstream_gene_variant MALY-DE 15 43322365 43322365 single base substitution A G intron_variant MALY-DE 15 43322365 43322365 single base substitution A G upstream_gene_variant MALY-DE 15 43324018 43324018 single base substitution A T intron_variant MALY-DE 15 43324018 43324018 single base substitution A T upstream_gene_variant MALY-DE 15 43329439 43329439 single base substitution G C intron_variant MALY-DE 15 43341816 43341816 single base substitution A G intron_variant MALY-DE 15 43346031 43346031 single base substitution T G intron_variant MALY-DE 15 43352344 43352344 single base substitution T C intron_variant MALY-DE 15 43352344 43352344 single base substitution T C upstream_gene_variant MALY-DE 15 43354181 43354181 single base substitution A T intron_variant MALY-DE 15 43354181 43354181 single base substitution A T upstream_gene_variant MALY-DE 15 43355367 43355367 single base substitution A G intron_variant MALY-DE 15 43355367 43355367 single base substitution A G upstream_gene_variant MALY-DE 15 43362945 43362945 single base substitution T A intron_variant MALY-DE 15 43376167 43376167 single base substitution G A intron_variant MALY-DE 15 43378930 43378930 single base substitution G A intron_variant MALY-DE 15 43385641 43385641 single base substitution T G intron_variant MALY-DE 15 43387377 43387377 single base substitution T C intron_variant MALY-DE 15 43389052 43389052 single base substitution T A intron_variant MALY-DE 15 43390464 43390464 single base substitution A G intron_variant MALY-DE 15 43397057 43397057 single base substitution T C intron_variant MALY-DE 15 43398344 43398344 single base substitution C T upstream_gene_variant MELA-AU 15 43230395 43230395 single base substitution A T downstream_gene_variant MELA-AU 15 43230452 43230452 single base substitution A C downstream_gene_variant MELA-AU 15 43230483 43230483 single base substitution G A downstream_gene_variant MELA-AU 15 43230807 43230807 single base substitution A G downstream_gene_variant MELA-AU 15 43230842 43230842 single base substitution C T downstream_gene_variant MELA-AU 15 43232728 43232728 single base substitution C T downstream_gene_variant MELA-AU 15 43233261 43233261 single base substitution G A downstream_gene_variant MELA-AU 15 43233413 43233413 single base substitution C T downstream_gene_variant MELA-AU 15 43235075 43235075 single base substitution C T downstream_gene_variant MELA-AU 15 43235214 43235214 single base substitution A G 3_prime_UTR_variant MELA-AU 15 43235214 43235214 single base substitution A G downstream_gene_variant MELA-AU 15 43235677 43235677 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43235677 43235677 single base substitution G A downstream_gene_variant MELA-AU 15 43236225 43236225 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43236225 43236225 single base substitution G A downstream_gene_variant MELA-AU 15 43237097 43237097 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43237097 43237097 single base substitution G A downstream_gene_variant MELA-AU 15 43239889 43239889 single base substitution C T intron_variant MELA-AU 15 43239910 43239910 single base substitution G A intron_variant MELA-AU 15 43241451 43241451 single base substitution G A intron_variant MELA-AU 15 43241499 43241499 single base substitution G A intron_variant MELA-AU 15 43241542 43241542 single base substitution G A intron_variant MELA-AU 15 43241929 43241929 single base substitution A G intron_variant MELA-AU 15 43242592 43242592 single base substitution T C exon_variant MELA-AU 15 43242592 43242592 single base substitution T C intron_variant MELA-AU 15 43243086 43243086 single base substitution G A intron_variant MELA-AU 15 43243086 43243086 single base substitution G A upstream_gene_variant MELA-AU 15 43243501 43243501 single base substitution A G intron_variant MELA-AU 15 43243501 43243501 single base substitution A G upstream_gene_variant MELA-AU 15 43243611 43243611 single base substitution G A intron_variant MELA-AU 15 43243611 43243611 single base substitution G A upstream_gene_variant MELA-AU 15 43243673 43243673 single base substitution G A intron_variant MELA-AU 15 43243673 43243673 single base substitution G A upstream_gene_variant MELA-AU 15 43243890 43243890 single base substitution G A intron_variant MELA-AU 15 43243890 43243890 single base substitution G A upstream_gene_variant MELA-AU 15 43244030 43244030 single base substitution G T intron_variant MELA-AU 15 43244030 43244030 single base substitution G T upstream_gene_variant MELA-AU 15 43244080 43244080 single base substitution G A intron_variant MELA-AU 15 43244080 43244080 single base substitution G A upstream_gene_variant MELA-AU 15 43244481 43244481 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43244481 43244481 single base substitution G A synonymous_variant F1667F 5001C>T MELA-AU 15 43244481 43244481 single base substitution G A upstream_gene_variant MELA-AU 15 43244496 43244497 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 15 43244496 43244497 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant A1662V 4985CC>TT MELA-AU 15 43244496 43244497 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 43246715 43246715 single base substitution C T intron_variant MELA-AU 15 43246715 43246715 single base substitution C T upstream_gene_variant MELA-AU 15 43247149 43247149 single base substitution G A intron_variant MELA-AU 15 43247149 43247149 single base substitution G A upstream_gene_variant MELA-AU 15 43248212 43248212 single base substitution G A intron_variant MELA-AU 15 43248579 43248579 single base substitution A C intron_variant MELA-AU 15 43248722 43248722 single base substitution C G intron_variant MELA-AU 15 43248738 43248738 single base substitution G A intron_variant MELA-AU 15 43249089 43249089 single base substitution G A intron_variant MELA-AU 15 43249439 43249439 single base substitution A T intron_variant MELA-AU 15 43250126 43250126 single base substitution G A intron_variant MELA-AU 15 43250971 43250971 single base substitution C G intron_variant MELA-AU 15 43251231 43251231 single base substitution G A intron_variant MELA-AU 15 43252397 43252397 single base substitution A T intron_variant MELA-AU 15 43252793 43252793 single base substitution G A intron_variant MELA-AU 15 43253471 43253471 single base substitution C A intron_variant MELA-AU 15 43254550 43254550 single base substitution G A intron_variant MELA-AU 15 43255499 43255499 single base substitution G A intron_variant MELA-AU 15 43255507 43255507 single base substitution G A intron_variant MELA-AU 15 43256138 43256138 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43256138 43256138 single base substitution G A synonymous_variant L1565L 4695C>T MELA-AU 15 43256655 43256655 single base substitution G A intron_variant MELA-AU 15 43257099 43257099 single base substitution G A intron_variant MELA-AU 15 43257199 43257199 single base substitution G A intron_variant MELA-AU 15 43257452 43257452 single base substitution G A intron_variant MELA-AU 15 43258132 43258132 single base substitution G A intron_variant MELA-AU 15 43258141 43258141 single base substitution G A intron_variant MELA-AU 15 43258244 43258244 single base substitution G A intron_variant MELA-AU 15 43258783 43258783 single base substitution G A intron_variant MELA-AU 15 43258803 43258803 single base substitution G A intron_variant MELA-AU 15 43258863 43258863 single base substitution G A intron_variant MELA-AU 15 43259002 43259002 single base substitution C T intron_variant MELA-AU 15 43259398 43259398 single base substitution G A intron_variant MELA-AU 15 43259927 43259927 single base substitution C T intron_variant MELA-AU 15 43260128 43260128 single base substitution T A intron_variant MELA-AU 15 43261915 43261915 single base substitution G A intron_variant MELA-AU 15 43262913 43262913 single base substitution G A intron_variant MELA-AU 15 43262916 43262916 single base substitution G A intron_variant MELA-AU 15 43263252 43263252 single base substitution A C intron_variant MELA-AU 15 43263413 43263413 single base substitution G A intron_variant MELA-AU 15 43263492 43263493 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 43264514 43264514 single base substitution G A intron_variant MELA-AU 15 43264760 43264760 single base substitution G A intron_variant MELA-AU 15 43266431 43266431 single base substitution G A intron_variant MELA-AU 15 43267607 43267607 single base substitution G A intron_variant MELA-AU 15 43267761 43267761 single base substitution A T intron_variant MELA-AU 15 43267863 43267864 multiple base substitution (>=2bp and <=200bp) CC TG intron_variant MELA-AU 15 43268173 43268173 single base substitution C T intron_variant MELA-AU 15 43268588 43268588 single base substitution G A intron_variant MELA-AU 15 43268840 43268840 single base substitution C T intron_variant MELA-AU 15 43270137 43270137 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43270137 43270137 single base substitution G A missense_variant P1387S 4159C>T MELA-AU 15 43270227 43270227 single base substitution A T intron_variant MELA-AU 15 43270375 43270375 single base substitution G A intron_variant MELA-AU 15 43270587 43270587 single base substitution G A intron_variant MELA-AU 15 43271564 43271564 single base substitution A G intron_variant MELA-AU 15 43272063 43272063 single base substitution G A intron_variant MELA-AU 15 43273882 43273882 single base substitution G A intron_variant MELA-AU 15 43275331 43275331 single base substitution G A intron_variant MELA-AU 15 43277676 43277676 single base substitution C T downstream_gene_variant MELA-AU 15 43277676 43277676 single base substitution C T intron_variant MELA-AU 15 43278561 43278561 single base substitution G A downstream_gene_variant MELA-AU 15 43278561 43278561 single base substitution G A intron_variant MELA-AU 15 43278582 43278582 single base substitution A G downstream_gene_variant MELA-AU 15 43278582 43278582 single base substitution A G intron_variant MELA-AU 15 43278623 43278623 single base substitution T C downstream_gene_variant MELA-AU 15 43278623 43278623 single base substitution T C intron_variant MELA-AU 15 43278951 43278951 single base substitution T C downstream_gene_variant MELA-AU 15 43278951 43278951 single base substitution T C intron_variant MELA-AU 15 43279026 43279026 single base substitution G A downstream_gene_variant MELA-AU 15 43279026 43279026 single base substitution G A intron_variant MELA-AU 15 43279602 43279602 single base substitution G A downstream_gene_variant MELA-AU 15 43279602 43279602 single base substitution G A intron_variant MELA-AU 15 43279612 43279613 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 43279612 43279613 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 43279897 43279897 single base substitution G A downstream_gene_variant MELA-AU 15 43279897 43279897 single base substitution G A intron_variant MELA-AU 15 43280084 43280084 single base substitution G A downstream_gene_variant MELA-AU 15 43280084 43280084 single base substitution G A intron_variant MELA-AU 15 43280308 43280308 single base substitution G C downstream_gene_variant MELA-AU 15 43280308 43280308 single base substitution G C intron_variant MELA-AU 15 43280467 43280467 single base substitution A G downstream_gene_variant MELA-AU 15 43280467 43280467 single base substitution A G intron_variant MELA-AU 15 43281687 43281687 single base substitution G A intron_variant MELA-AU 15 43281807 43281807 single base substitution G A intron_variant MELA-AU 15 43282148 43282148 single base substitution G A intron_variant MELA-AU 15 43282334 43282334 single base substitution G A intron_variant MELA-AU 15 43282607 43282607 single base substitution G A intron_variant MELA-AU 15 43282659 43282659 single base substitution C T intron_variant MELA-AU 15 43282874 43282874 single base substitution C T intron_variant MELA-AU 15 43283715 43283715 single base substitution G A intron_variant MELA-AU 15 43283775 43283776 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 15 43284226 43284226 single base substitution A G intron_variant MELA-AU 15 43285400 43285400 single base substitution G A intron_variant MELA-AU 15 43286812 43286812 single base substitution A G intron_variant MELA-AU 15 43287524 43287524 single base substitution A G intron_variant MELA-AU 15 43287648 43287648 single base substitution G A intron_variant MELA-AU 15 43288804 43288804 deletion of <=200bp C - intron_variant MELA-AU 15 43289104 43289104 single base substitution G A intron_variant MELA-AU 15 43289249 43289249 single base substitution G A intron_variant MELA-AU 15 43291242 43291242 single base substitution G A downstream_gene_variant MELA-AU 15 43291242 43291242 single base substitution G A intron_variant MELA-AU 15 43291242 43291242 single base substitution G A upstream_gene_variant MELA-AU 15 43291710 43291710 single base substitution G A downstream_gene_variant MELA-AU 15 43291710 43291710 single base substitution G A intron_variant MELA-AU 15 43291710 43291710 single base substitution G A upstream_gene_variant MELA-AU 15 43292738 43292738 single base substitution G A downstream_gene_variant MELA-AU 15 43292738 43292738 single base substitution G A intron_variant MELA-AU 15 43292738 43292738 single base substitution G A upstream_gene_variant MELA-AU 15 43292762 43292762 single base substitution G A downstream_gene_variant MELA-AU 15 43292762 43292762 single base substitution G A intron_variant MELA-AU 15 43292762 43292762 single base substitution G A upstream_gene_variant MELA-AU 15 43292806 43292806 single base substitution T A downstream_gene_variant MELA-AU 15 43292806 43292806 single base substitution T A intron_variant MELA-AU 15 43292806 43292806 single base substitution T A upstream_gene_variant MELA-AU 15 43293368 43293368 single base substitution G A downstream_gene_variant MELA-AU 15 43293368 43293368 single base substitution G A intron_variant MELA-AU 15 43293368 43293368 single base substitution G A upstream_gene_variant MELA-AU 15 43293562 43293562 single base substitution G A downstream_gene_variant MELA-AU 15 43293562 43293562 single base substitution G A intron_variant MELA-AU 15 43293562 43293562 single base substitution G A upstream_gene_variant MELA-AU 15 43293773 43293773 single base substitution T C downstream_gene_variant MELA-AU 15 43293773 43293773 single base substitution T C intron_variant MELA-AU 15 43293773 43293773 single base substitution T C upstream_gene_variant MELA-AU 15 43294515 43294515 single base substitution G T downstream_gene_variant MELA-AU 15 43294515 43294515 single base substitution G T intron_variant MELA-AU 15 43294515 43294515 single base substitution G T upstream_gene_variant MELA-AU 15 43294676 43294676 single base substitution C T downstream_gene_variant MELA-AU 15 43294676 43294676 single base substitution C T intron_variant MELA-AU 15 43294676 43294676 single base substitution C T upstream_gene_variant MELA-AU 15 43294785 43294785 single base substitution G T 3_prime_UTR_variant MELA-AU 15 43294785 43294785 single base substitution G T downstream_gene_variant MELA-AU 15 43294785 43294785 single base substitution G T synonymous_variant P1209P 3627C>A MELA-AU 15 43294785 43294785 single base substitution G T upstream_gene_variant MELA-AU 15 43295331 43295331 single base substitution G A downstream_gene_variant MELA-AU 15 43295331 43295331 single base substitution G A intron_variant MELA-AU 15 43295331 43295331 single base substitution G A upstream_gene_variant MELA-AU 15 43295446 43295446 single base substitution A G downstream_gene_variant MELA-AU 15 43295446 43295446 single base substitution A G intron_variant MELA-AU 15 43295476 43295476 single base substitution G A exon_variant MELA-AU 15 43295476 43295476 single base substitution G A intron_variant MELA-AU 15 43296769 43296769 single base substitution G A intron_variant MELA-AU 15 43297568 43297568 single base substitution G A intron_variant MELA-AU 15 43297658 43297658 single base substitution G A intron_variant MELA-AU 15 43297824 43297824 single base substitution G A intron_variant MELA-AU 15 43298986 43298986 single base substitution G A intron_variant MELA-AU 15 43299512 43299512 single base substitution C T intron_variant MELA-AU 15 43299713 43299713 single base substitution G A intron_variant MELA-AU 15 43299835 43299835 single base substitution A G intron_variant MELA-AU 15 43300738 43300738 single base substitution G A intron_variant MELA-AU 15 43300796 43300796 single base substitution G A intron_variant MELA-AU 15 43300814 43300814 single base substitution G A intron_variant MELA-AU 15 43300839 43300839 single base substitution G A intron_variant MELA-AU 15 43301173 43301173 single base substitution C T intron_variant MELA-AU 15 43301610 43301610 single base substitution G A intron_variant MELA-AU 15 43302205 43302205 single base substitution G A intron_variant MELA-AU 15 43302736 43302736 single base substitution G A intron_variant MELA-AU 15 43303094 43303094 single base substitution G A downstream_gene_variant MELA-AU 15 43303094 43303094 single base substitution G A intron_variant MELA-AU 15 43303095 43303095 single base substitution G A downstream_gene_variant MELA-AU 15 43303095 43303095 single base substitution G A intron_variant MELA-AU 15 43303440 43303440 single base substitution A T downstream_gene_variant MELA-AU 15 43303440 43303440 single base substitution A T intron_variant MELA-AU 15 43303585 43303585 single base substitution T A downstream_gene_variant MELA-AU 15 43303585 43303585 single base substitution T A intron_variant MELA-AU 15 43304543 43304543 deletion of <=200bp G - downstream_gene_variant MELA-AU 15 43304543 43304543 deletion of <=200bp G - intron_variant MELA-AU 15 43305055 43305055 single base substitution G A downstream_gene_variant MELA-AU 15 43305055 43305055 single base substitution G A intron_variant MELA-AU 15 43305373 43305373 single base substitution G A downstream_gene_variant MELA-AU 15 43305373 43305373 single base substitution G A intron_variant MELA-AU 15 43305382 43305382 single base substitution G A downstream_gene_variant MELA-AU 15 43305382 43305382 single base substitution G A intron_variant MELA-AU 15 43306161 43306161 single base substitution G A downstream_gene_variant MELA-AU 15 43306161 43306161 single base substitution G A intron_variant MELA-AU 15 43306350 43306350 single base substitution G A downstream_gene_variant MELA-AU 15 43306350 43306350 single base substitution G A intron_variant MELA-AU 15 43306977 43306977 single base substitution G A downstream_gene_variant MELA-AU 15 43306977 43306977 single base substitution G A intron_variant MELA-AU 15 43307161 43307161 single base substitution G T downstream_gene_variant MELA-AU 15 43307161 43307161 single base substitution G T intron_variant MELA-AU 15 43307264 43307264 single base substitution G A downstream_gene_variant MELA-AU 15 43307264 43307264 single base substitution G A intron_variant MELA-AU 15 43307920 43307920 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43307920 43307920 single base substitution G A exon_variant MELA-AU 15 43307920 43307920 single base substitution G A missense_variant P1059S 3175C>T MELA-AU 15 43308603 43308603 single base substitution A G downstream_gene_variant MELA-AU 15 43308603 43308603 single base substitution A G intron_variant MELA-AU 15 43308603 43308603 single base substitution A G upstream_gene_variant MELA-AU 15 43309318 43309318 single base substitution C A 3_prime_UTR_variant MELA-AU 15 43309318 43309318 single base substitution C A downstream_gene_variant MELA-AU 15 43309318 43309318 single base substitution C A exon_variant MELA-AU 15 43309318 43309318 single base substitution C A missense_variant G1001V 3002G>T MELA-AU 15 43309318 43309318 single base substitution C A upstream_gene_variant MELA-AU 15 43309327 43309327 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43309327 43309327 single base substitution G A downstream_gene_variant MELA-AU 15 43309327 43309327 single base substitution G A exon_variant MELA-AU 15 43309327 43309327 single base substitution G A missense_variant T998I 2993C>T MELA-AU 15 43309327 43309327 single base substitution G A upstream_gene_variant MELA-AU 15 43309735 43309735 single base substitution G A downstream_gene_variant MELA-AU 15 43309735 43309735 single base substitution G A intron_variant MELA-AU 15 43309735 43309735 single base substitution G A upstream_gene_variant MELA-AU 15 43310720 43310720 single base substitution G A downstream_gene_variant MELA-AU 15 43310720 43310720 single base substitution G A intron_variant MELA-AU 15 43310720 43310720 single base substitution G A upstream_gene_variant MELA-AU 15 43311530 43311530 single base substitution G A downstream_gene_variant MELA-AU 15 43311530 43311530 single base substitution G A intron_variant MELA-AU 15 43311530 43311530 single base substitution G A upstream_gene_variant MELA-AU 15 43311884 43311884 single base substitution G A downstream_gene_variant MELA-AU 15 43311884 43311884 single base substitution G A intron_variant MELA-AU 15 43311884 43311884 single base substitution G A upstream_gene_variant MELA-AU 15 43313272 43313272 single base substitution G A downstream_gene_variant MELA-AU 15 43313272 43313272 single base substitution G A intron_variant MELA-AU 15 43313326 43313326 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43313326 43313326 single base substitution G A intron_variant MELA-AU 15 43313352 43313352 single base substitution T C 3_prime_UTR_variant MELA-AU 15 43313352 43313352 single base substitution T C intron_variant MELA-AU 15 43313820 43313820 single base substitution T C intron_variant MELA-AU 15 43313823 43313823 single base substitution G A intron_variant MELA-AU 15 43313913 43313913 single base substitution G A intron_variant MELA-AU 15 43314115 43314115 single base substitution A G intron_variant MELA-AU 15 43314137 43314137 single base substitution C T intron_variant MELA-AU 15 43314685 43314685 single base substitution T A intron_variant MELA-AU 15 43315373 43315373 single base substitution G A intron_variant MELA-AU 15 43315710 43315710 single base substitution A G intron_variant MELA-AU 15 43316814 43316814 single base substitution G A intron_variant MELA-AU 15 43317195 43317195 single base substitution G A intron_variant MELA-AU 15 43317200 43317200 single base substitution G A intron_variant MELA-AU 15 43318221 43318221 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43318221 43318221 single base substitution G A intron_variant MELA-AU 15 43318759 43318759 single base substitution C T 3_prime_UTR_variant MELA-AU 15 43318759 43318759 single base substitution C T splice_region_variant MELA-AU 15 43318805 43318805 single base substitution T C 3_prime_UTR_variant MELA-AU 15 43318805 43318805 single base substitution T C exon_variant MELA-AU 15 43318805 43318805 single base substitution T C missense_variant D19G 56A>G MELA-AU 15 43318805 43318805 single base substitution T C missense_variant D830G 2489A>G MELA-AU 15 43318886 43318886 single base substitution G A intron_variant MELA-AU 15 43318886 43318886 single base substitution G A upstream_gene_variant MELA-AU 15 43319289 43319289 single base substitution T C intron_variant MELA-AU 15 43319289 43319289 single base substitution T C upstream_gene_variant MELA-AU 15 43320162 43320162 insertion of <=200bp - T intron_variant MELA-AU 15 43320162 43320162 insertion of <=200bp - T upstream_gene_variant MELA-AU 15 43320532 43320532 single base substitution G A intron_variant MELA-AU 15 43320532 43320532 single base substitution G A upstream_gene_variant MELA-AU 15 43321191 43321191 single base substitution G A intron_variant MELA-AU 15 43321191 43321191 single base substitution G A upstream_gene_variant MELA-AU 15 43321588 43321588 single base substitution G A intron_variant MELA-AU 15 43321588 43321588 single base substitution G A upstream_gene_variant MELA-AU 15 43322196 43322196 insertion of <=200bp - C exon_variant MELA-AU 15 43322196 43322196 insertion of <=200bp - C frameshift_variant L775L? MELA-AU 15 43322196 43322196 insertion of <=200bp - C upstream_gene_variant MELA-AU 15 43322799 43322799 single base substitution T C intron_variant MELA-AU 15 43322799 43322799 single base substitution T C upstream_gene_variant MELA-AU 15 43323940 43323941 multiple base substitution (>=2bp and <=200bp) GC TT intron_variant MELA-AU 15 43323940 43323941 multiple base substitution (>=2bp and <=200bp) GC TT upstream_gene_variant MELA-AU 15 43325104 43325104 single base substitution A G intron_variant MELA-AU 15 43325538 43325538 single base substitution G C intron_variant MELA-AU 15 43326123 43326123 single base substitution G A intron_variant MELA-AU 15 43326488 43326488 single base substitution A G intron_variant MELA-AU 15 43328019 43328019 single base substitution G A intron_variant MELA-AU 15 43328291 43328291 single base substitution G A intron_variant MELA-AU 15 43328739 43328739 single base substitution A C exon_variant MELA-AU 15 43328739 43328739 single base substitution A C missense_variant I692S 2075T>G MELA-AU 15 43328851 43328851 single base substitution C T intron_variant MELA-AU 15 43328854 43328854 single base substitution G A intron_variant MELA-AU 15 43329322 43329322 single base substitution G A intron_variant MELA-AU 15 43332059 43332059 single base substitution C T downstream_gene_variant MELA-AU 15 43332059 43332059 single base substitution C T intron_variant MELA-AU 15 43332059 43332059 single base substitution C T upstream_gene_variant MELA-AU 15 43332286 43332286 single base substitution G A downstream_gene_variant MELA-AU 15 43332286 43332286 single base substitution G A intron_variant MELA-AU 15 43332286 43332286 single base substitution G A upstream_gene_variant MELA-AU 15 43332830 43332830 single base substitution G A downstream_gene_variant MELA-AU 15 43332830 43332830 single base substitution G A intron_variant MELA-AU 15 43332830 43332830 single base substitution G A upstream_gene_variant MELA-AU 15 43332843 43332843 single base substitution G A downstream_gene_variant MELA-AU 15 43332843 43332843 single base substitution G A intron_variant MELA-AU 15 43332843 43332843 single base substitution G A upstream_gene_variant MELA-AU 15 43333616 43333616 single base substitution G A downstream_gene_variant MELA-AU 15 43333616 43333616 single base substitution G A intron_variant MELA-AU 15 43333616 43333616 single base substitution G A upstream_gene_variant MELA-AU 15 43334343 43334343 single base substitution T C downstream_gene_variant MELA-AU 15 43334343 43334343 single base substitution T C intron_variant MELA-AU 15 43334343 43334343 single base substitution T C upstream_gene_variant MELA-AU 15 43334717 43334717 single base substitution G A downstream_gene_variant MELA-AU 15 43334717 43334717 single base substitution G A intron_variant MELA-AU 15 43334717 43334717 single base substitution G A upstream_gene_variant MELA-AU 15 43335145 43335145 single base substitution G A downstream_gene_variant MELA-AU 15 43335145 43335145 single base substitution G A intron_variant MELA-AU 15 43336126 43336126 single base substitution G A intron_variant MELA-AU 15 43336128 43336128 single base substitution G A intron_variant MELA-AU 15 43336129 43336129 single base substitution G A intron_variant MELA-AU 15 43337159 43337159 single base substitution A C intron_variant MELA-AU 15 43337271 43337271 single base substitution T A intron_variant MELA-AU 15 43337430 43337430 single base substitution G A intron_variant MELA-AU 15 43338041 43338041 single base substitution A G intron_variant MELA-AU 15 43338571 43338571 single base substitution A T intron_variant MELA-AU 15 43338671 43338671 single base substitution G A intron_variant MELA-AU 15 43338915 43338915 single base substitution G A intron_variant MELA-AU 15 43339438 43339438 single base substitution G A 3_prime_UTR_variant MELA-AU 15 43339438 43339438 single base substitution G A exon_variant MELA-AU 15 43339438 43339438 single base substitution G A missense_variant P530L 1589C>T MELA-AU 15 43339830 43339830 single base substitution G A intron_variant MELA-AU 15 43340747 43340747 single base substitution G A intron_variant MELA-AU 15 43341067 43341067 single base substitution G A intron_variant MELA-AU 15 43341479 43341479 single base substitution A T intron_variant MELA-AU 15 43341627 43341627 single base substitution G T intron_variant MELA-AU 15 43341797 43341797 single base substitution G A intron_variant MELA-AU 15 43343146 43343146 single base substitution G A intron_variant MELA-AU 15 43343271 43343271 single base substitution G A intron_variant MELA-AU 15 43343558 43343558 single base substitution G A intron_variant MELA-AU 15 43343762 43343762 single base substitution G A intron_variant MELA-AU 15 43343822 43343822 single base substitution C T intron_variant MELA-AU 15 43344893 43344893 single base substitution G A intron_variant MELA-AU 15 43345008 43345008 single base substitution G A intron_variant MELA-AU 15 43347296 43347296 single base substitution A G intron_variant MELA-AU 15 43347879 43347879 single base substitution A G intron_variant MELA-AU 15 43348290 43348291 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 43348801 43348801 single base substitution A G intron_variant MELA-AU 15 43348882 43348882 single base substitution A T intron_variant MELA-AU 15 43349050 43349050 single base substitution G A intron_variant MELA-AU 15 43349293 43349293 single base substitution A G intron_variant MELA-AU 15 43349325 43349325 single base substitution G A intron_variant MELA-AU 15 43349885 43349887 deletion of <=200bp TTC - intron_variant MELA-AU 15 43350894 43350894 single base substitution T A intron_variant MELA-AU 15 43350973 43350973 single base substitution C A intron_variant MELA-AU 15 43351403 43351403 single base substitution G A intron_variant MELA-AU 15 43351540 43351540 single base substitution G A intron_variant MELA-AU 15 43351706 43351706 single base substitution G A intron_variant MELA-AU 15 43352037 43352037 single base substitution G A intron_variant MELA-AU 15 43352037 43352037 single base substitution G A upstream_gene_variant MELA-AU 15 43352781 43352781 single base substitution G A intron_variant MELA-AU 15 43352781 43352781 single base substitution G A upstream_gene_variant MELA-AU 15 43352935 43352935 single base substitution G A intron_variant MELA-AU 15 43352935 43352935 single base substitution G A upstream_gene_variant MELA-AU 15 43353583 43353583 single base substitution G A intron_variant MELA-AU 15 43353583 43353583 single base substitution G A upstream_gene_variant MELA-AU 15 43353603 43353603 single base substitution C G intron_variant MELA-AU 15 43353603 43353603 single base substitution C G upstream_gene_variant MELA-AU 15 43353604 43353604 single base substitution G A intron_variant MELA-AU 15 43353604 43353604 single base substitution G A upstream_gene_variant MELA-AU 15 43354109 43354109 single base substitution A G intron_variant MELA-AU 15 43354109 43354109 single base substitution A G upstream_gene_variant MELA-AU 15 43354374 43354374 single base substitution G A intron_variant MELA-AU 15 43354374 43354374 single base substitution G A upstream_gene_variant MELA-AU 15 43354666 43354666 single base substitution G A intron_variant MELA-AU 15 43354666 43354666 single base substitution G A upstream_gene_variant MELA-AU 15 43355583 43355583 single base substitution G T intron_variant MELA-AU 15 43355583 43355583 single base substitution G T upstream_gene_variant MELA-AU 15 43355704 43355704 single base substitution A G intron_variant MELA-AU 15 43355704 43355704 single base substitution A G upstream_gene_variant MELA-AU 15 43355718 43355719 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 43355718 43355719 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 43355975 43355976 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 43355975 43355976 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 43356579 43356579 single base substitution A G intron_variant MELA-AU 15 43356579 43356579 single base substitution A G upstream_gene_variant MELA-AU 15 43357648 43357648 single base substitution A G intron_variant MELA-AU 15 43357685 43357685 single base substitution G A intron_variant MELA-AU 15 43358420 43358420 single base substitution G A intron_variant MELA-AU 15 43359410 43359410 insertion of <=200bp - T intron_variant MELA-AU 15 43359554 43359554 deletion of <=200bp A - intron_variant MELA-AU 15 43359560 43359560 single base substitution G T intron_variant MELA-AU 15 43359671 43359671 single base substitution C T intron_variant MELA-AU 15 43360512 43360512 single base substitution A C intron_variant MELA-AU 15 43361382 43361382 single base substitution C T intron_variant MELA-AU 15 43361505 43361505 single base substitution C G intron_variant MELA-AU 15 43361741 43361741 single base substitution G A intron_variant MELA-AU 15 43361743 43361743 single base substitution G A intron_variant MELA-AU 15 43361893 43361893 single base substitution G A intron_variant MELA-AU 15 43362522 43362522 single base substitution G A intron_variant MELA-AU 15 43362544 43362544 single base substitution C T intron_variant MELA-AU 15 43363232 43363232 single base substitution C T intron_variant MELA-AU 15 43364086 43364086 single base substitution G A intron_variant MELA-AU 15 43364888 43364888 single base substitution G A intron_variant MELA-AU 15 43365306 43365307 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 43366128 43366128 single base substitution G A intron_variant MELA-AU 15 43366910 43366910 single base substitution C T intron_variant MELA-AU 15 43367805 43367805 single base substitution G A intron_variant MELA-AU 15 43368303 43368303 single base substitution C A intron_variant MELA-AU 15 43369837 43369837 single base substitution G A intron_variant MELA-AU 15 43370285 43370285 single base substitution A T downstream_gene_variant MELA-AU 15 43370285 43370285 single base substitution A T intron_variant MELA-AU 15 43370454 43370454 single base substitution G A downstream_gene_variant MELA-AU 15 43370454 43370454 single base substitution G A intron_variant MELA-AU 15 43370525 43370525 single base substitution G A downstream_gene_variant MELA-AU 15 43370525 43370525 single base substitution G A intron_variant MELA-AU 15 43371803 43371804 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 43371803 43371804 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 43372876 43372876 single base substitution G A downstream_gene_variant MELA-AU 15 43372876 43372876 single base substitution G A intron_variant MELA-AU 15 43373834 43373834 single base substitution G A downstream_gene_variant MELA-AU 15 43373834 43373834 single base substitution G A intron_variant MELA-AU 15 43375045 43375045 single base substitution G A intron_variant MELA-AU 15 43375480 43375480 single base substitution C A intron_variant MELA-AU 15 43375713 43375713 single base substitution G A intron_variant MELA-AU 15 43375723 43375723 single base substitution C A intron_variant MELA-AU 15 43376788 43376788 single base substitution G A intron_variant MELA-AU 15 43377300 43377300 single base substitution C T intron_variant MELA-AU 15 43377996 43377996 single base substitution C T intron_variant MELA-AU 15 43378138 43378138 single base substitution G A intron_variant MELA-AU 15 43378567 43378567 single base substitution G A intron_variant MELA-AU 15 43379670 43379670 single base substitution G A intron_variant MELA-AU 15 43380901 43380901 single base substitution G A intron_variant MELA-AU 15 43381354 43381354 single base substitution C T intron_variant MELA-AU 15 43381440 43381440 single base substitution C T intron_variant MELA-AU 15 43381536 43381536 single base substitution A G intron_variant MELA-AU 15 43381814 43381814 single base substitution C T intron_variant MELA-AU 15 43381905 43381905 single base substitution G A intron_variant MELA-AU 15 43382076 43382076 single base substitution G A intron_variant MELA-AU 15 43382270 43382270 single base substitution G A intron_variant MELA-AU 15 43382285 43382285 single base substitution G A intron_variant MELA-AU 15 43382566 43382566 single base substitution C T intron_variant MELA-AU 15 43382643 43382643 single base substitution A G intron_variant MELA-AU 15 43383626 43383626 single base substitution C T intron_variant MELA-AU 15 43384350 43384351 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 43385891 43385891 single base substitution G A intron_variant MELA-AU 15 43385965 43385965 single base substitution G A intron_variant MELA-AU 15 43386183 43386183 single base substitution A T intron_variant MELA-AU 15 43387933 43387933 single base substitution G A intron_variant MELA-AU 15 43389085 43389085 single base substitution G A intron_variant MELA-AU 15 43390331 43390332 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 43392097 43392097 single base substitution G A intron_variant MELA-AU 15 43392696 43392696 single base substitution C T intron_variant MELA-AU 15 43393172 43393172 single base substitution G A intron_variant MELA-AU 15 43394199 43394199 single base substitution A C intron_variant MELA-AU 15 43395924 43395924 single base substitution G A intron_variant MELA-AU 15 43396232 43396232 single base substitution C T intron_variant MELA-AU 15 43397488 43397488 single base substitution C T intron_variant MELA-AU 15 43398336 43398336 single base substitution G A upstream_gene_variant MELA-AU 15 43398418 43398418 single base substitution C T upstream_gene_variant MELA-AU 15 43399181 43399181 single base substitution G C upstream_gene_variant MELA-AU 15 43399369 43399369 single base substitution G A upstream_gene_variant MELA-AU 15 43399643 43399643 single base substitution G A upstream_gene_variant MELA-AU 15 43399800 43399800 single base substitution C G upstream_gene_variant MELA-AU 15 43400351 43400351 single base substitution T C upstream_gene_variant MELA-AU 15 43400833 43400833 single base substitution C T upstream_gene_variant MELA-AU 15 43401007 43401007 single base substitution G A upstream_gene_variant MELA-AU 15 43401538 43401538 single base substitution G A upstream_gene_variant MELA-AU 15 43401557 43401557 single base substitution C T upstream_gene_variant MELA-AU 15 43401568 43401569 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 43401597 43401597 single base substitution C T upstream_gene_variant MELA-AU 15 43402064 43402064 single base substitution C T upstream_gene_variant MELA-AU 15 43402320 43402320 single base substitution G A upstream_gene_variant MELA-AU 15 43402328 43402328 single base substitution G A upstream_gene_variant MELA-AU 15 43402549 43402549 single base substitution G A upstream_gene_variant MELA-AU 15 43402652 43402652 single base substitution G A upstream_gene_variant MELA-AU 15 43403264 43403264 single base substitution G A upstream_gene_variant MELA-AU 15 43403267 43403267 single base substitution G A upstream_gene_variant MELA-AU 15 43403299 43403299 single base substitution G A upstream_gene_variant ORCA-IN 15 43242841 43242841 single base substitution C T intron_variant ORCA-IN 15 43242841 43242841 single base substitution C T upstream_gene_variant ORCA-IN 15 43242962 43242962 single base substitution C T intron_variant ORCA-IN 15 43242962 43242962 single base substitution C T upstream_gene_variant ORCA-IN 15 43280385 43280385 single base substitution C T downstream_gene_variant ORCA-IN 15 43280385 43280385 single base substitution C T intron_variant ORCA-IN 15 43306032 43306032 single base substitution C T downstream_gene_variant ORCA-IN 15 43306032 43306032 single base substitution C T intron_variant ORCA-IN 15 43307989 43307989 single base substitution G A 3_prime_UTR_variant ORCA-IN 15 43307989 43307989 single base substitution G A exon_variant ORCA-IN 15 43307989 43307989 single base substitution G A stop_gained Q1036* 3106C>T ORCA-IN 15 43328664 43328664 single base substitution C T intron_variant ORCA-IN 15 43351802 43351803 deletion of <=200bp AG - intron_variant ORCA-IN 15 43370350 43370350 single base substitution G A downstream_gene_variant ORCA-IN 15 43370350 43370350 single base substitution G A intron_variant OV-AU 15 43262511 43262511 single base substitution C A intron_variant OV-AU 15 43270040 43270040 single base substitution C T intron_variant OV-AU 15 43270041 43270041 single base substitution A T intron_variant OV-AU 15 43270047 43270047 single base substitution A T intron_variant OV-AU 15 43294575 43294575 single base substitution G A downstream_gene_variant OV-AU 15 43294575 43294575 single base substitution G A intron_variant OV-AU 15 43294575 43294575 single base substitution G A upstream_gene_variant OV-AU 15 43297505 43297505 single base substitution C T intron_variant OV-AU 15 43299876 43299876 single base substitution C A intron_variant OV-AU 15 43307078 43307078 single base substitution T G downstream_gene_variant OV-AU 15 43307078 43307078 single base substitution T G intron_variant OV-AU 15 43309865 43309865 single base substitution G T downstream_gene_variant OV-AU 15 43309865 43309865 single base substitution G T intron_variant OV-AU 15 43309865 43309865 single base substitution G T upstream_gene_variant OV-AU 15 43311168 43311168 single base substitution G A downstream_gene_variant OV-AU 15 43311168 43311168 single base substitution G A intron_variant OV-AU 15 43311168 43311168 single base substitution G A upstream_gene_variant OV-AU 15 43320547 43320547 single base substitution T A intron_variant OV-AU 15 43320547 43320547 single base substitution T A upstream_gene_variant OV-AU 15 43320957 43320957 single base substitution A C intron_variant OV-AU 15 43320957 43320957 single base substitution A C upstream_gene_variant OV-AU 15 43332974 43332974 single base substitution G A downstream_gene_variant OV-AU 15 43332974 43332974 single base substitution G A intron_variant OV-AU 15 43332974 43332974 single base substitution G A upstream_gene_variant OV-AU 15 43334933 43334933 single base substitution A G downstream_gene_variant OV-AU 15 43334933 43334933 single base substitution A G intron_variant OV-AU 15 43334933 43334933 single base substitution A G upstream_gene_variant OV-AU 15 43348437 43348437 single base substitution T C intron_variant OV-AU 15 43363967 43363967 single base substitution C A intron_variant OV-AU 15 43368616 43368616 single base substitution G C intron_variant OV-AU 15 43370229 43370229 single base substitution A G downstream_gene_variant OV-AU 15 43370229 43370229 single base substitution A G intron_variant OV-AU 15 43371070 43371070 single base substitution C G downstream_gene_variant OV-AU 15 43371070 43371070 single base substitution C G intron_variant OV-AU 15 43381303 43381303 single base substitution T G intron_variant OV-AU 15 43383659 43383659 single base substitution A C intron_variant OV-AU 15 43393984 43393984 single base substitution G C intron_variant PACA-AU 15 43233077 43233077 single base substitution C A downstream_gene_variant PACA-AU 15 43233381 43233381 single base substitution T G downstream_gene_variant PACA-AU 15 43236699 43236699 single base substitution T C 3_prime_UTR_variant PACA-AU 15 43236699 43236699 single base substitution T C downstream_gene_variant PACA-AU 15 43245754 43245754 single base substitution A C intron_variant PACA-AU 15 43245754 43245754 single base substitution A C upstream_gene_variant PACA-AU 15 43251075 43251075 single base substitution C A intron_variant PACA-AU 15 43253314 43253314 single base substitution T C intron_variant PACA-AU 15 43264295 43264295 single base substitution A C intron_variant PACA-AU 15 43277701 43277701 single base substitution C A downstream_gene_variant PACA-AU 15 43277701 43277701 single base substitution C A intron_variant PACA-AU 15 43277702 43277702 single base substitution C A downstream_gene_variant PACA-AU 15 43277702 43277702 single base substitution C A intron_variant PACA-AU 15 43281126 43281126 single base substitution G T 3_prime_UTR_variant PACA-AU 15 43281126 43281126 single base substitution G T exon_variant PACA-AU 15 43281126 43281126 single base substitution G T synonymous_variant L1296L 3888C>A PACA-AU 15 43283277 43283277 single base substitution A T intron_variant PACA-AU 15 43286493 43286493 single base substitution C G intron_variant PACA-AU 15 43289281 43289281 single base substitution G C intron_variant PACA-AU 15 43292738 43292738 single base substitution G C downstream_gene_variant PACA-AU 15 43292738 43292738 single base substitution G C intron_variant PACA-AU 15 43292738 43292738 single base substitution G C upstream_gene_variant PACA-AU 15 43296482 43296482 single base substitution T C intron_variant PACA-AU 15 43305501 43305501 single base substitution A C downstream_gene_variant PACA-AU 15 43305501 43305501 single base substitution A C intron_variant PACA-AU 15 43306255 43306255 deletion of <=200bp T - downstream_gene_variant PACA-AU 15 43306255 43306255 deletion of <=200bp T - intron_variant PACA-AU 15 43307217 43307217 single base substitution G A downstream_gene_variant PACA-AU 15 43307217 43307217 single base substitution G A intron_variant PACA-AU 15 43314623 43314623 single base substitution T A intron_variant PACA-AU 15 43317838 43317838 single base substitution T C 3_prime_UTR_variant PACA-AU 15 43317838 43317838 single base substitution T C intron_variant PACA-AU 15 43340020 43340021 deletion of <=200bp TA - intron_variant PACA-AU 15 43345764 43345764 single base substitution G A intron_variant PACA-AU 15 43346522 43346522 single base substitution T C intron_variant PACA-AU 15 43364454 43364454 single base substitution T A intron_variant PACA-AU 15 43367315 43367315 single base substitution G C intron_variant PACA-AU 15 43368191 43368191 single base substitution G C intron_variant PACA-AU 15 43376482 43376482 single base substitution C T intron_variant PACA-AU 15 43385941 43385941 single base substitution G A intron_variant PACA-AU 15 43395221 43395221 single base substitution C A intron_variant PACA-AU 15 43395961 43395961 single base substitution A G intron_variant PACA-AU 15 43398108 43398108 deletion of <=200bp A - intron_variant PACA-AU 15 43401732 43401732 single base substitution C T upstream_gene_variant PACA-CA 15 43230897 43230897 single base substitution G A downstream_gene_variant PACA-CA 15 43233947 43233947 single base substitution C A downstream_gene_variant PACA-CA 15 43235690 43235707 deletion of <=200bp TGGCAGTAAAGGTCTGGC - 3_prime_UTR_variant PACA-CA 15 43235690 43235707 deletion of <=200bp TGGCAGTAAAGGTCTGGC - downstream_gene_variant PACA-CA 15 43240356 43240356 single base substitution C A intron_variant PACA-CA 15 43243689 43243689 single base substitution G T intron_variant PACA-CA 15 43243689 43243689 single base substitution G T upstream_gene_variant PACA-CA 15 43244948 43244948 single base substitution G A intron_variant PACA-CA 15 43244948 43244948 single base substitution G A upstream_gene_variant PACA-CA 15 43246202 43246202 single base substitution T A intron_variant PACA-CA 15 43246202 43246202 single base substitution T A upstream_gene_variant PACA-CA 15 43248956 43248956 single base substitution C T intron_variant PACA-CA 15 43254541 43254541 single base substitution G A intron_variant PACA-CA 15 43258892 43258892 single base substitution A T intron_variant PACA-CA 15 43262696 43262696 single base substitution G T intron_variant PACA-CA 15 43273442 43273442 insertion of <=200bp - A intron_variant PACA-CA 15 43275218 43275218 single base substitution A G intron_variant PACA-CA 15 43280462 43280462 insertion of <=200bp - AT downstream_gene_variant PACA-CA 15 43280462 43280462 insertion of <=200bp - AT intron_variant PACA-CA 15 43281485 43281485 single base substitution C G intron_variant PACA-CA 15 43283239 43283239 single base substitution G A intron_variant PACA-CA 15 43285054 43285054 single base substitution A G intron_variant PACA-CA 15 43286557 43286557 single base substitution G A intron_variant PACA-CA 15 43288593 43288593 single base substitution G C intron_variant PACA-CA 15 43297457 43297457 single base substitution C A intron_variant PACA-CA 15 43297493 43297493 single base substitution G C intron_variant PACA-CA 15 43299123 43299123 single base substitution A G intron_variant PACA-CA 15 43299774 43299774 single base substitution C T intron_variant PACA-CA 15 43303087 43303087 single base substitution T C downstream_gene_variant PACA-CA 15 43303087 43303087 single base substitution T C intron_variant PACA-CA 15 43306282 43306282 single base substitution G A downstream_gene_variant PACA-CA 15 43306282 43306282 single base substitution G A intron_variant PACA-CA 15 43309408 43309408 single base substitution A G downstream_gene_variant PACA-CA 15 43309408 43309408 single base substitution A G intron_variant PACA-CA 15 43309408 43309408 single base substitution A G upstream_gene_variant PACA-CA 15 43310254 43310254 single base substitution G A downstream_gene_variant PACA-CA 15 43310254 43310254 single base substitution G A intron_variant PACA-CA 15 43310254 43310254 single base substitution G A upstream_gene_variant PACA-CA 15 43313912 43313912 single base substitution C T intron_variant PACA-CA 15 43315063 43315063 single base substitution A C intron_variant PACA-CA 15 43315123 43315123 single base substitution C T intron_variant PACA-CA 15 43316491 43316491 single base substitution A G intron_variant PACA-CA 15 43316540 43316540 single base substitution T C intron_variant PACA-CA 15 43318395 43318395 single base substitution G A 3_prime_UTR_variant PACA-CA 15 43318395 43318395 single base substitution G A intron_variant PACA-CA 15 43324618 43324618 single base substitution T C intron_variant PACA-CA 15 43324618 43324618 single base substitution T C upstream_gene_variant PACA-CA 15 43331618 43331618 single base substitution A G downstream_gene_variant PACA-CA 15 43331618 43331618 single base substitution A G intron_variant PACA-CA 15 43331618 43331618 single base substitution A G upstream_gene_variant PACA-CA 15 43332280 43332280 single base substitution G A downstream_gene_variant PACA-CA 15 43332280 43332280 single base substitution G A intron_variant PACA-CA 15 43332280 43332280 single base substitution G A upstream_gene_variant PACA-CA 15 43336132 43336132 deletion of <=200bp A - intron_variant PACA-CA 15 43337329 43337329 single base substitution G A intron_variant PACA-CA 15 43343102 43343102 single base substitution A G intron_variant PACA-CA 15 43344790 43344790 single base substitution A G intron_variant PACA-CA 15 43345801 43345801 deletion of <=200bp T - intron_variant PACA-CA 15 43351431 43351431 single base substitution C T intron_variant PACA-CA 15 43355531 43355531 single base substitution C T intron_variant PACA-CA 15 43355531 43355531 single base substitution C T upstream_gene_variant PACA-CA 15 43356521 43356521 single base substitution G A intron_variant PACA-CA 15 43356521 43356521 single base substitution G A upstream_gene_variant PACA-CA 15 43357405 43357405 single base substitution A G intron_variant PACA-CA 15 43359507 43359507 single base substitution C A intron_variant PACA-CA 15 43360954 43360954 single base substitution G T intron_variant PACA-CA 15 43364969 43364969 single base substitution G A intron_variant PACA-CA 15 43367037 43367037 insertion of <=200bp - A intron_variant PACA-CA 15 43380986 43380986 single base substitution A G intron_variant PACA-CA 15 43384442 43384442 single base substitution G A intron_variant PACA-CA 15 43384607 43384607 single base substitution G C intron_variant PACA-CA 15 43387909 43387909 single base substitution G C intron_variant PACA-CA 15 43389671 43389671 single base substitution T G intron_variant PACA-CA 15 43389881 43389881 single base substitution G A intron_variant PACA-CA 15 43395945 43395945 single base substitution T C intron_variant PACA-CA 15 43400415 43400415 single base substitution G T upstream_gene_variant PACA-CA 15 43400922 43400922 single base substitution A C upstream_gene_variant PACA-CA 15 43402437 43402437 single base substitution C G upstream_gene_variant PACA-CA 15 43403029 43403029 single base substitution A T upstream_gene_variant PAEN-AU 15 43289860 43289860 single base substitution C T intron_variant PAEN-AU 15 43307004 43307004 single base substitution C T downstream_gene_variant PAEN-AU 15 43307004 43307004 single base substitution C T intron_variant PAEN-AU 15 43307050 43307050 single base substitution C T downstream_gene_variant PAEN-AU 15 43307050 43307050 single base substitution C T intron_variant PAEN-AU 15 43328734 43328734 single base substitution T C exon_variant PAEN-AU 15 43328734 43328734 single base substitution T C missense_variant M694V 2080A>G PAEN-AU 15 43365342 43365342 single base substitution C A intron_variant PAEN-IT 15 43253312 43253312 single base substitution T C intron_variant PAEN-IT 15 43302365 43302365 single base substitution C T intron_variant PAEN-IT 15 43317522 43317522 single base substitution T A intron_variant PAEN-IT 15 43375146 43375146 single base substitution C A intron_variant PAEN-IT 15 43395259 43395259 single base substitution G T intron_variant PBCA-DE 15 43230946 43230946 single base substitution C A downstream_gene_variant PBCA-DE 15 43239423 43239423 single base substitution C A intron_variant PBCA-DE 15 43241941 43241941 single base substitution G T intron_variant PBCA-DE 15 43263121 43263121 single base substitution C T intron_variant PBCA-DE 15 43282227 43282227 insertion of <=200bp - CCC splice_donor_variant PBCA-DE 15 43297772 43297786 deletion of <=200bp ACCCCGTCTGGGAGG - intron_variant PBCA-DE 15 43299593 43299593 single base substitution T A intron_variant PBCA-DE 15 43333549 43333549 single base substitution C A downstream_gene_variant PBCA-DE 15 43333549 43333549 single base substitution C A intron_variant PBCA-DE 15 43333549 43333549 single base substitution C A upstream_gene_variant PBCA-DE 15 43340534 43340534 single base substitution C T intron_variant PBCA-DE 15 43340617 43340617 single base substitution A T 3_prime_UTR_variant PBCA-DE 15 43340617 43340617 single base substitution A T exon_variant PBCA-DE 15 43340617 43340617 single base substitution A T intron_variant PBCA-DE 15 43340617 43340617 single base substitution A T synonymous_variant S504S 1512T>A PBCA-DE 15 43346181 43346181 single base substitution C T intron_variant PBCA-DE 15 43380796 43380796 single base substitution C G intron_variant PBCA-DE 15 43384892 43384892 single base substitution C T intron_variant PBCA-DE 15 43385640 43385640 single base substitution C A intron_variant PBCA-DE 15 43392710 43392710 single base substitution T C intron_variant PBCA-DE 15 43402881 43402881 insertion of <=200bp - A upstream_gene_variant PRAD-CA 15 43241420 43241420 single base substitution T A intron_variant PRAD-CA 15 43265505 43265505 single base substitution G A intron_variant PRAD-CA 15 43271185 43271185 single base substitution C T intron_variant PRAD-CA 15 43316373 43316373 single base substitution A C intron_variant PRAD-CA 15 43328878 43328878 single base substitution C G intron_variant PRAD-CA 15 43346753 43346753 single base substitution T G intron_variant PRAD-CA 15 43368252 43368252 single base substitution C G intron_variant PRAD-CA 15 43374815 43374815 single base substitution G A downstream_gene_variant PRAD-CA 15 43374815 43374815 single base substitution G A intron_variant PRAD-CA 15 43385103 43385103 single base substitution C G intron_variant PRAD-CA 15 43385791 43385791 single base substitution C T intron_variant PRAD-CA 15 43401568 43401568 single base substitution G A upstream_gene_variant PRAD-UK 15 43255824 43255824 single base substitution G A intron_variant PRAD-UK 15 43265535 43265535 single base substitution C A intron_variant PRAD-UK 15 43283063 43283063 single base substitution C A intron_variant PRAD-UK 15 43293086 43293086 single base substitution C A downstream_gene_variant PRAD-UK 15 43293086 43293086 single base substitution C A intron_variant PRAD-UK 15 43293086 43293086 single base substitution C A upstream_gene_variant PRAD-UK 15 43295770 43295770 insertion of <=200bp - T intron_variant PRAD-UK 15 43298135 43298135 single base substitution G T intron_variant PRAD-UK 15 43298258 43298258 single base substitution G T intron_variant PRAD-UK 15 43306523 43306524 deletion of <=200bp GT - downstream_gene_variant PRAD-UK 15 43306523 43306524 deletion of <=200bp GT - intron_variant PRAD-UK 15 43306524 43306525 deletion of <=200bp TC - downstream_gene_variant PRAD-UK 15 43306524 43306525 deletion of <=200bp TC - intron_variant PRAD-UK 15 43307716 43307716 single base substitution G A downstream_gene_variant PRAD-UK 15 43307716 43307716 single base substitution G A intron_variant PRAD-UK 15 43333430 43333430 single base substitution G A downstream_gene_variant PRAD-UK 15 43333430 43333430 single base substitution G A intron_variant PRAD-UK 15 43333430 43333430 single base substitution G A upstream_gene_variant PRAD-UK 15 43346651 43346651 single base substitution G A intron_variant PRAD-UK 15 43363071 43363071 single base substitution A C exon_variant PRAD-UK 15 43363071 43363071 single base substitution A C intron_variant PRAD-UK 15 43363071 43363071 single base substitution A C missense_variant F194C 581T>G PRAD-UK 15 43372229 43372229 single base substitution C T downstream_gene_variant PRAD-UK 15 43372229 43372229 single base substitution C T intron_variant PRAD-UK 15 43373780 43373780 single base substitution T G downstream_gene_variant PRAD-UK 15 43373780 43373780 single base substitution T G intron_variant PRAD-UK 15 43374547 43374547 insertion of <=200bp - GAGCAAAGAGCTCAAA downstream_gene_variant PRAD-UK 15 43374547 43374547 insertion of <=200bp - GAGCAAAGAGCTCAAA intron_variant PRAD-UK 15 43375677 43375677 single base substitution C T intron_variant PRAD-UK 15 43388129 43388129 single base substitution A T intron_variant PRAD-US 15 43242542 43242542 single base substitution C G 3_prime_UTR_variant PRAD-US 15 43242542 43242542 single base substitution C G exon_variant PRAD-US 15 43242542 43242542 single base substitution C G missense_variant V1676L 5026G>C PRAD-US 15 43262758 43262758 single base substitution C T 3_prime_UTR_variant PRAD-US 15 43262758 43262758 single base substitution C T missense_variant A1473T 4417G>A PRAD-US 15 43276106 43276106 single base substitution C T 3_prime_UTR_variant PRAD-US 15 43276106 43276106 single base substitution C T downstream_gene_variant PRAD-US 15 43276106 43276106 single base substitution C T missense_variant R1380H 4139G>A READ-US 15 43281141 43281141 single base substitution C A 3_prime_UTR_variant READ-US 15 43281141 43281141 single base substitution C A exon_variant READ-US 15 43281141 43281141 single base substitution C A missense_variant K1291N 3873G>T READ-US 15 43367232 43367232 single base substitution T G 3_prime_UTR_variant READ-US 15 43367232 43367232 single base substitution T G exon_variant READ-US 15 43367232 43367232 single base substitution T G missense_variant K158T 473A>C RECA-EU 15 43233590 43233590 single base substitution A C downstream_gene_variant RECA-EU 15 43237962 43237962 single base substitution T A intron_variant RECA-EU 15 43237963 43237963 single base substitution A T intron_variant RECA-EU 15 43283794 43283794 single base substitution T C intron_variant RECA-EU 15 43295713 43295713 single base substitution C T intron_variant RECA-EU 15 43295781 43295781 single base substitution G A intron_variant RECA-EU 15 43305661 43305661 single base substitution C T downstream_gene_variant RECA-EU 15 43305661 43305661 single base substitution C T intron_variant RECA-EU 15 43308651 43308651 single base substitution T C downstream_gene_variant RECA-EU 15 43308651 43308651 single base substitution T C intron_variant RECA-EU 15 43308651 43308651 single base substitution T C upstream_gene_variant RECA-EU 15 43310287 43310287 single base substitution G A downstream_gene_variant RECA-EU 15 43310287 43310287 single base substitution G A intron_variant RECA-EU 15 43310287 43310287 single base substitution G A upstream_gene_variant RECA-EU 15 43319198 43319198 single base substitution A G intron_variant RECA-EU 15 43319198 43319198 single base substitution A G upstream_gene_variant RECA-EU 15 43336452 43336452 single base substitution A G intron_variant RECA-EU 15 43339440 43339440 single base substitution A G 3_prime_UTR_variant RECA-EU 15 43339440 43339440 single base substitution A G exon_variant RECA-EU 15 43339440 43339440 single base substitution A G synonymous_variant D529D 1587T>C RECA-EU 15 43340806 43340806 single base substitution T G intron_variant RECA-EU 15 43357837 43357837 single base substitution A C intron_variant RECA-EU 15 43367284 43367284 single base substitution G T 3_prime_UTR_variant RECA-EU 15 43367284 43367284 single base substitution G T exon_variant RECA-EU 15 43367284 43367284 single base substitution G T missense_variant H141N 421C>A RECA-EU 15 43380034 43380034 single base substitution T A intron_variant RECA-EU 15 43381727 43381727 single base substitution A T intron_variant RECA-EU 15 43387668 43387668 single base substitution C T intron_variant RECA-EU 15 43387889 43387889 single base substitution T C intron_variant RECA-EU 15 43401434 43401434 single base substitution G A upstream_gene_variant SKCA-BR 15 43231327 43231327 single base substitution A C downstream_gene_variant SKCA-BR 15 43234271 43234271 single base substitution T A downstream_gene_variant SKCA-BR 15 43234302 43234302 single base substitution C T downstream_gene_variant SKCA-BR 15 43235366 43235366 single base substitution A G 3_prime_UTR_variant SKCA-BR 15 43235366 43235366 single base substitution A G downstream_gene_variant SKCA-BR 15 43237017 43237017 single base substitution A T 3_prime_UTR_variant SKCA-BR 15 43237017 43237017 single base substitution A T downstream_gene_variant SKCA-BR 15 43245635 43245635 single base substitution G A intron_variant SKCA-BR 15 43245635 43245635 single base substitution G A upstream_gene_variant SKCA-BR 15 43248505 43248505 single base substitution T C intron_variant SKCA-BR 15 43250158 43250158 single base substitution G A intron_variant SKCA-BR 15 43252219 43252219 single base substitution G A intron_variant SKCA-BR 15 43253180 43253180 single base substitution A C intron_variant SKCA-BR 15 43254119 43254119 insertion of <=200bp - AT intron_variant SKCA-BR 15 43257918 43257918 single base substitution G A intron_variant SKCA-BR 15 43258241 43258241 single base substitution G A intron_variant SKCA-BR 15 43258242 43258242 single base substitution G A intron_variant SKCA-BR 15 43259558 43259558 single base substitution G A intron_variant SKCA-BR 15 43264463 43264463 single base substitution G A intron_variant SKCA-BR 15 43266701 43266701 single base substitution A G intron_variant SKCA-BR 15 43270322 43270322 single base substitution G A intron_variant SKCA-BR 15 43273911 43273911 single base substitution A C intron_variant SKCA-BR 15 43275028 43275028 single base substitution C T intron_variant SKCA-BR 15 43276322 43276322 single base substitution C T downstream_gene_variant SKCA-BR 15 43276322 43276322 single base substitution C T intron_variant SKCA-BR 15 43280333 43280333 single base substitution C T downstream_gene_variant SKCA-BR 15 43280333 43280333 single base substitution C T intron_variant SKCA-BR 15 43280467 43280467 insertion of <=200bp - ATG downstream_gene_variant SKCA-BR 15 43280467 43280467 insertion of <=200bp - ATG intron_variant SKCA-BR 15 43280930 43280930 single base substitution G A exon_variant SKCA-BR 15 43280930 43280930 single base substitution G A intron_variant SKCA-BR 15 43281832 43281832 single base substitution G A intron_variant SKCA-BR 15 43286702 43286702 single base substitution C T intron_variant SKCA-BR 15 43286723 43286723 single base substitution A C intron_variant SKCA-BR 15 43287632 43287632 single base substitution T G intron_variant SKCA-BR 15 43287635 43287635 single base substitution A G intron_variant SKCA-BR 15 43289398 43289398 single base substitution G A intron_variant SKCA-BR 15 43289638 43289638 single base substitution G A intron_variant SKCA-BR 15 43291448 43291448 single base substitution C T downstream_gene_variant SKCA-BR 15 43291448 43291448 single base substitution C T intron_variant SKCA-BR 15 43291448 43291448 single base substitution C T upstream_gene_variant SKCA-BR 15 43294801 43294801 single base substitution C A 3_prime_UTR_variant SKCA-BR 15 43294801 43294801 single base substitution C A downstream_gene_variant SKCA-BR 15 43294801 43294801 single base substitution C A missense_variant C1204F 3611G>T SKCA-BR 15 43294801 43294801 single base substitution C A upstream_gene_variant SKCA-BR 15 43295582 43295582 single base substitution G A intron_variant SKCA-BR 15 43295582 43295582 single base substitution G A splice_region_variant SKCA-BR 15 43297523 43297523 single base substitution G A intron_variant SKCA-BR 15 43297663 43297663 single base substitution A G intron_variant SKCA-BR 15 43301101 43301101 single base substitution G A intron_variant SKCA-BR 15 43306174 43306174 single base substitution T C downstream_gene_variant SKCA-BR 15 43306174 43306174 single base substitution T C intron_variant SKCA-BR 15 43307207 43307211 deletion of <=200bp TGGGA - downstream_gene_variant SKCA-BR 15 43307207 43307211 deletion of <=200bp TGGGA - intron_variant SKCA-BR 15 43307600 43307600 single base substitution G A downstream_gene_variant SKCA-BR 15 43307600 43307600 single base substitution G A intron_variant SKCA-BR 15 43309018 43309018 single base substitution A C downstream_gene_variant SKCA-BR 15 43309018 43309018 single base substitution A C intron_variant SKCA-BR 15 43309018 43309018 single base substitution A C upstream_gene_variant SKCA-BR 15 43309022 43309022 single base substitution A C downstream_gene_variant SKCA-BR 15 43309022 43309022 single base substitution A C intron_variant SKCA-BR 15 43309022 43309022 single base substitution A C upstream_gene_variant SKCA-BR 15 43310392 43310392 single base substitution G C downstream_gene_variant SKCA-BR 15 43310392 43310392 single base substitution G C intron_variant SKCA-BR 15 43310392 43310392 single base substitution G C upstream_gene_variant SKCA-BR 15 43321440 43321440 single base substitution C T intron_variant SKCA-BR 15 43321440 43321440 single base substitution C T upstream_gene_variant SKCA-BR 15 43325846 43325846 single base substitution C T intron_variant SKCA-BR 15 43326435 43326447 deletion of <=200bp AAAATAAATAAAT - intron_variant SKCA-BR 15 43327086 43327091 deletion of <=200bp CAAAAA - intron_variant SKCA-BR 15 43327099 43327099 single base substitution A C intron_variant SKCA-BR 15 43327117 43327117 single base substitution G A intron_variant SKCA-BR 15 43333805 43333805 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 15 43333805 43333805 insertion of <=200bp - CA intron_variant SKCA-BR 15 43333805 43333805 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 15 43337417 43337417 single base substitution G A intron_variant SKCA-BR 15 43342259 43342259 single base substitution C T intron_variant SKCA-BR 15 43342260 43342260 single base substitution C T intron_variant SKCA-BR 15 43342921 43342921 insertion of <=200bp - TA intron_variant SKCA-BR 15 43348285 43348285 single base substitution T C intron_variant SKCA-BR 15 43351786 43351787 deletion of <=200bp CA - intron_variant SKCA-BR 15 43351803 43351803 single base substitution G A intron_variant SKCA-BR 15 43353660 43353660 single base substitution T A intron_variant SKCA-BR 15 43353660 43353660 single base substitution T A upstream_gene_variant SKCA-BR 15 43354652 43354652 single base substitution G A intron_variant SKCA-BR 15 43354652 43354652 single base substitution G A upstream_gene_variant SKCA-BR 15 43356775 43356775 insertion of <=200bp - CT intron_variant SKCA-BR 15 43356775 43356775 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 15 43359625 43359625 single base substitution G A intron_variant SKCA-BR 15 43360276 43360276 single base substitution T A intron_variant SKCA-BR 15 43360308 43360308 single base substitution C A intron_variant SKCA-BR 15 43361615 43361615 single base substitution C G intron_variant SKCA-BR 15 43364270 43364270 single base substitution G A intron_variant SKCA-BR 15 43364370 43364370 single base substitution C T intron_variant SKCA-BR 15 43368427 43368427 single base substitution G A intron_variant SKCA-BR 15 43368853 43368853 single base substitution A C intron_variant SKCA-BR 15 43369415 43369415 single base substitution A G intron_variant SKCA-BR 15 43369424 43369424 single base substitution A G intron_variant SKCA-BR 15 43371077 43371077 single base substitution G A downstream_gene_variant SKCA-BR 15 43371077 43371077 single base substitution G A intron_variant SKCA-BR 15 43372571 43372571 single base substitution T C downstream_gene_variant SKCA-BR 15 43372571 43372571 single base substitution T C intron_variant SKCA-BR 15 43379426 43379426 single base substitution A C intron_variant SKCA-BR 15 43390010 43390010 single base substitution T G intron_variant SKCA-BR 15 43390640 43390640 single base substitution A G intron_variant SKCA-BR 15 43391635 43391635 single base substitution C T intron_variant SKCA-BR 15 43391782 43391782 single base substitution C T intron_variant SKCA-BR 15 43392240 43392241 deletion of <=200bp AT - intron_variant SKCA-BR 15 43392904 43392904 single base substitution G A intron_variant SKCA-BR 15 43395322 43395322 single base substitution C A intron_variant SKCA-BR 15 43397838 43397838 single base substitution A C intron_variant SKCA-BR 15 43398035 43398035 single base substitution T C intron_variant SKCA-BR 15 43398108 43398108 single base substitution A G intron_variant SKCA-BR 15 43401597 43401597 single base substitution C T upstream_gene_variant SKCA-BR 15 43402919 43402919 single base substitution C T upstream_gene_variant SKCM-US 15 43244481 43244481 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43244481 43244481 single base substitution G A synonymous_variant F1667F 5001C>T SKCM-US 15 43244481 43244481 single base substitution G A upstream_gene_variant SKCM-US 15 43244516 43244516 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43244516 43244516 single base substitution G A missense_variant H1656Y 4966C>T SKCM-US 15 43244516 43244516 single base substitution G A upstream_gene_variant SKCM-US 15 43262760 43262760 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43262760 43262760 single base substitution G A missense_variant S1472F 4415C>T SKCM-US 15 43269007 43269007 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43269007 43269007 single base substitution G A missense_variant P1426L 4277C>T SKCM-US 15 43269030 43269030 single base substitution C T 3_prime_UTR_variant SKCM-US 15 43269030 43269030 single base substitution C T stop_gained W1418* 4254G>A SKCM-US 15 43269040 43269040 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43269040 43269040 single base substitution G A missense_variant S1415F 4244C>T SKCM-US 15 43299340 43299340 single base substitution C T 3_prime_UTR_variant SKCM-US 15 43299340 43299340 single base substitution C T exon_variant SKCM-US 15 43299340 43299340 single base substitution C T missense_variant A1118T 3352G>A SKCM-US 15 43299342 43299342 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43299342 43299342 single base substitution G A exon_variant SKCM-US 15 43299342 43299342 single base substitution G A missense_variant S1117L 3350C>T SKCM-US 15 43307948 43307948 single base substitution T C 3_prime_UTR_variant SKCM-US 15 43307948 43307948 single base substitution T C exon_variant SKCM-US 15 43307948 43307948 single base substitution T C synonymous_variant K1049K 3147A>G SKCM-US 15 43314912 43314912 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43314912 43314912 single base substitution G A exon_variant SKCM-US 15 43314912 43314912 single base substitution G A missense_variant H132Y 394C>T SKCM-US 15 43314912 43314912 single base substitution G A missense_variant H943Y 2827C>T SKCM-US 15 43317039 43317039 single base substitution C T 3_prime_UTR_variant SKCM-US 15 43317039 43317039 single base substitution C T exon_variant SKCM-US 15 43317039 43317039 single base substitution C T synonymous_variant G909G 2727G>A SKCM-US 15 43317039 43317039 single base substitution C T synonymous_variant G98G 294G>A SKCM-US 15 43318759 43318759 single base substitution C T 3_prime_UTR_variant SKCM-US 15 43318759 43318759 single base substitution C T splice_region_variant SKCM-US 15 43328430 43328430 deletion of <=200bp A - exon_variant SKCM-US 15 43328430 43328430 deletion of <=200bp A - frameshift_variant L712 SKCM-US 15 43339380 43339380 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43339380 43339380 single base substitution G A exon_variant SKCM-US 15 43339380 43339380 single base substitution G A synonymous_variant F549F 1647C>T SKCM-US 15 43339438 43339438 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43339438 43339438 single base substitution G A exon_variant SKCM-US 15 43339438 43339438 single base substitution G A missense_variant P530L 1589C>T SKCM-US 15 43340622 43340622 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43340622 43340622 single base substitution G A exon_variant SKCM-US 15 43340622 43340622 single base substitution G A intron_variant SKCM-US 15 43340622 43340622 single base substitution G A stop_gained R503* 1507C>T SKCM-US 15 43351289 43351289 single base substitution A G exon_variant SKCM-US 15 43351289 43351289 single base substitution A G intron_variant SKCM-US 15 43351289 43351289 single base substitution A G missense_variant Y363H 1087T>C SKCM-US 15 43351929 43351929 single base substitution G A exon_variant SKCM-US 15 43351929 43351929 single base substitution G A intron_variant SKCM-US 15 43351929 43351929 single base substitution G A missense_variant S319F 956C>T SKCM-US 15 43360109 43360109 single base substitution G C exon_variant SKCM-US 15 43360109 43360109 single base substitution G C intron_variant SKCM-US 15 43360109 43360109 single base substitution G C missense_variant A262G 785C>G SKCM-US 15 43363004 43363004 single base substitution T A exon_variant SKCM-US 15 43363004 43363004 single base substitution T A intron_variant SKCM-US 15 43363004 43363004 single base substitution T A missense_variant E216D 648A>T SKCM-US 15 43363063 43363063 single base substitution C T exon_variant SKCM-US 15 43363063 43363063 single base substitution C T intron_variant SKCM-US 15 43363063 43363063 single base substitution C T missense_variant V197M 589G>A SKCM-US 15 43363110 43363110 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43363110 43363110 single base substitution G A exon_variant SKCM-US 15 43363110 43363110 single base substitution G A missense_variant P181L 542C>T SKCM-US 15 43367225 43367225 single base substitution G A 3_prime_UTR_variant SKCM-US 15 43367225 43367225 single base substitution G A exon_variant SKCM-US 15 43367225 43367225 single base substitution G A synonymous_variant G160G 480C>T STAD-US 15 43237587 43237587 single base substitution C T 3_prime_UTR_variant STAD-US 15 43237587 43237587 single base substitution C T exon_variant STAD-US 15 43237587 43237587 single base substitution C T synonymous_variant E1730E 5190G>A STAD-US 15 43237655 43237655 deletion of <=200bp G - 3_prime_UTR_variant STAD-US 15 43237655 43237655 deletion of <=200bp G - exon_variant STAD-US 15 43237655 43237655 deletion of <=200bp G - frameshift_variant L1708 STAD-US 15 43244513 43244513 single base substitution C T 3_prime_UTR_variant STAD-US 15 43244513 43244513 single base substitution C T missense_variant A1657T 4969G>A STAD-US 15 43244513 43244513 single base substitution C T upstream_gene_variant STAD-US 15 43252855 43252855 insertion of <=200bp - T 3_prime_UTR_variant STAD-US 15 43252855 43252855 insertion of <=200bp - T frameshift_variant N1582K? STAD-US 15 43258414 43258414 single base substitution G A 3_prime_UTR_variant STAD-US 15 43258414 43258414 single base substitution G A missense_variant R1510C 4528C>T STAD-US 15 43299296 43299296 deletion of <=200bp T - 3_prime_UTR_variant STAD-US 15 43299296 43299296 deletion of <=200bp T - exon_variant STAD-US 15 43299296 43299296 deletion of <=200bp T - frameshift_variant K1132 STAD-US 15 43308000 43308000 single base substitution T G 3_prime_UTR_variant STAD-US 15 43308000 43308000 single base substitution T G exon_variant STAD-US 15 43308000 43308000 single base substitution T G missense_variant K1032T 3095A>C STAD-US 15 43317086 43317086 single base substitution C T 3_prime_UTR_variant STAD-US 15 43317086 43317086 single base substitution C T exon_variant STAD-US 15 43317086 43317086 single base substitution C T missense_variant V83I 247G>A STAD-US 15 43317086 43317086 single base substitution C T missense_variant V894I 2680G>A STAD-US 15 43350584 43350584 deletion of <=200bp A - exon_variant STAD-US 15 43350584 43350584 deletion of <=200bp A - frameshift_variant F379 STAD-US 15 43350584 43350584 deletion of <=200bp A - intron_variant STAD-US 15 43351982 43351982 single base substitution T C exon_variant STAD-US 15 43351982 43351982 single base substitution T C intron_variant STAD-US 15 43351982 43351982 single base substitution T C synonymous_variant E301E 903A>G STAD-US 15 43367236 43367236 single base substitution A G 3_prime_UTR_variant STAD-US 15 43367236 43367236 single base substitution A G exon_variant STAD-US 15 43367236 43367236 single base substitution A G missense_variant W157R 469T>C STAD-US 15 43378309 43378309 single base substitution A G 3_prime_UTR_variant STAD-US 15 43378309 43378309 single base substitution A G exon_variant STAD-US 15 43378309 43378309 single base substitution A G intron_variant STAD-US 15 43378309 43378309 single base substitution A G missense_variant F71L 211T>C THCA-SA 15 43236612 43236612 single base substitution C T 3_prime_UTR_variant THCA-SA 15 43236612 43236612 single base substitution C T downstream_gene_variant THCA-SA 15 43237203 43237203 single base substitution T C 3_prime_UTR_variant THCA-SA 15 43237203 43237203 single base substitution T C downstream_gene_variant THCA-SA 15 43237414 43237414 single base substitution C T 3_prime_UTR_variant THCA-SA 15 43237414 43237414 single base substitution C T exon_variant THCA-US 15 43270075 43270075 insertion of <=200bp - A splice_region_variant THCA-US 15 43348594 43348594 single base substitution C G 3_prime_UTR_variant THCA-US 15 43348594 43348594 single base substitution C G exon_variant THCA-US 15 43348594 43348594 single base substitution C G intron_variant THCA-US 15 43348594 43348594 single base substitution C G missense_variant R410T 1229G>C UCEC-US 15 43237582 43237582 single base substitution G T 3_prime_UTR_variant UCEC-US 15 43237582 43237582 single base substitution G T exon_variant UCEC-US 15 43237582 43237582 single base substitution G T missense_variant A1732D 5195C>A UCEC-US 15 43250252 43250252 single base substitution A G 3_prime_UTR_variant UCEC-US 15 43250252 43250252 single base substitution A G synonymous_variant P1598P 4794T>C UCEC-US 15 43277128 43277128 single base substitution C T 3_prime_UTR_variant UCEC-US 15 43277128 43277128 single base substitution C T downstream_gene_variant UCEC-US 15 43277128 43277128 single base substitution C T missense_variant G1337E 4010G>A UCEC-US 15 43282296 43282296 single base substitution G T 3_prime_UTR_variant UCEC-US 15 43282296 43282296 single base substitution G T exon_variant UCEC-US 15 43282296 43282296 single base substitution G T missense_variant F1260L 3780C>A UCEC-US 15 43294867 43294867 single base substitution C T 3_prime_UTR_variant UCEC-US 15 43294867 43294867 single base substitution C T downstream_gene_variant UCEC-US 15 43294867 43294867 single base substitution C T missense_variant R1182H 3545G>A UCEC-US 15 43294867 43294867 single base substitution C T upstream_gene_variant UCEC-US 15 43296048 43296048 single base substitution C T 3_prime_UTR_variant UCEC-US 15 43296048 43296048 single base substitution C T exon_variant UCEC-US 15 43296048 43296048 single base substitution C T missense_variant V1166M 3496G>A UCEC-US 15 43307911 43307911 single base substitution C A 3_prime_UTR_variant UCEC-US 15 43307911 43307911 single base substitution C A exon_variant UCEC-US 15 43307911 43307911 single base substitution C A stop_gained E1062* 3184G>T UCEC-US 15 43308052 43308052 single base substitution C A 3_prime_UTR_variant UCEC-US 15 43308052 43308052 single base substitution C A exon_variant UCEC-US 15 43308052 43308052 single base substitution C A stop_gained E1015* 3043G>T UCEC-US 15 43317044 43317044 single base substitution C T 3_prime_UTR_variant UCEC-US 15 43317044 43317044 single base substitution C T exon_variant UCEC-US 15 43317044 43317044 single base substitution C T missense_variant E908K 2722G>A UCEC-US 15 43317044 43317044 single base substitution C T missense_variant E97K 289G>A UCEC-US 15 43318806 43318806 single base substitution C A 3_prime_UTR_variant UCEC-US 15 43318806 43318806 single base substitution C A exon_variant UCEC-US 15 43318806 43318806 single base substitution C A missense_variant D19Y 55G>T UCEC-US 15 43318806 43318806 single base substitution C A missense_variant D830Y 2488G>T UCEC-US 15 43324803 43324803 single base substitution T C exon_variant UCEC-US 15 43324803 43324803 single base substitution T C synonymous_variant L739L 2217A>G UCEC-US 15 43324803 43324803 single base substitution T C upstream_gene_variant UCEC-US 15 43328731 43328731 single base substitution G A exon_variant UCEC-US 15 43328731 43328731 single base substitution G A missense_variant L695F 2083C>T UCEC-US 15 43328743 43328743 single base substitution C A exon_variant UCEC-US 15 43328743 43328743 single base substitution C A missense_variant D691Y 2071G>T UCEC-US 15 43329975 43329975 single base substitution C A exon_variant UCEC-US 15 43329975 43329975 single base substitution C A missense_variant S673I 2018G>T UCEC-US 15 43339390 43339390 single base substitution A C 3_prime_UTR_variant UCEC-US 15 43339390 43339390 single base substitution A C exon_variant UCEC-US 15 43339390 43339390 single base substitution A C stop_gained L546* 1637T>G UCEC-US 15 43340621 43340621 single base substitution C T 3_prime_UTR_variant UCEC-US 15 43340621 43340621 single base substitution C T exon_variant UCEC-US 15 43340621 43340621 single base substitution C T intron_variant UCEC-US 15 43340621 43340621 single base substitution C T missense_variant R503Q 1508G>A UCEC-US 15 43347006 43347006 single base substitution T G exon_variant UCEC-US 15 43347006 43347006 single base substitution T G intron_variant UCEC-US 15 43347006 43347006 single base substitution T G missense_variant K458T 1373A>C UCEC-US 15 43347065 43347065 single base substitution G T exon_variant UCEC-US 15 43347065 43347065 single base substitution G T intron_variant UCEC-US 15 43347065 43347065 single base substitution G T synonymous_variant I438I 1314C>A UCEC-US 15 43351915 43351915 single base substitution T C exon_variant UCEC-US 15 43351915 43351915 single base substitution T C intron_variant UCEC-US 15 43351915 43351915 single base substitution T C missense_variant I324V 970A>G UCEC-US 15 43352006 43352006 single base substitution G A exon_variant UCEC-US 15 43352006 43352006 single base substitution G A intron_variant UCEC-US 15 43352006 43352006 single base substitution G A synonymous_variant V293V 879C>T UCEC-US 15 43352006 43352006 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LC_C12 COSM1188988 c.911A>G p.H304R Substitution - Missense 15:43059776-43059776 - CSCC-10-T COSM4453847 c.358A>G p.T120A Substitution - Missense 15:43082697-43082697 - TCGA-AP-A0LF-01 COSM961881 c.327C>A p.T109T Substitution - coding silent 15:43085995-43085995 - TCGA-B0-5696-01 COSM470658 c.4036G>A p.A1346T Substitution - Missense 15:42984904-42984904 - PD3890a COSM3664753 c.4460C>A p.S1487Y Substitution - Missense 15:42966284-42966284 - CHC892T COSM4960476 c.995G>A p.R332K Substitution - Missense 15:43059183-43059183 - CHC892T COSM4795602 c.1872G>A p.R624R Substitution - coding silent 15:43038210-43038210 - PT08_1 COSM5893851 c.4172C>T p.S1391L Substitution - Missense 15:42977926-42977926 - U343 COSM5712685 c.759C>T p.L253L Substitution - coding silent 15:43067937-43067937 - LUAD-5V8LT COSM401545 c.3495A>T p.A1165A Substitution - coding silent 15:43003851-43003851 - YUBER COSM1708067 c.802C>A p.R268S Substitution - Missense 15:43060111-43060111 - TCGA-BR-7703-01 COSM4054765 c.2680G>A p.V894I Substitution - Missense 15:43024888-43024888 - TCGA-B5-A11E-01 COSM961877 c.1373A>C p.K458T Substitution - Missense 15:43054808-43054808 - HCC017T COSM5815201 c.4912A>T p.N1638Y Substitution - Missense 15:42952372-42952372 - B80-3 COSM1749146 c.4548C>G p.F1516L Substitution - Missense 15:42966196-42966196 - HCC063T COSM5812590 c.3383A>T p.Q1128L Substitution - Missense 15:43007111-43007111 - SNUH_G16_S1 COSM3678189 c.4077G>A p.M1359I Substitution - Missense 15:42983970-42983970 - CSCC-6-T COSM4452726 c.208A>T p.I70L Substitution - Missense 15:43086114-43086114 - cSCCP6 COSM136999 c.3773C>T p.P1258L Substitution - Missense 15:42990105-42990105 - TCGA-FS-A4FC-06 COSM3501336 c.4277C>T p.P1426L Substitution - Missense 15:42976809-42976809 - TCGA-EE-A29D-06 COSM3501345 c.1087T>C p.Y363H Substitution - Missense 15:43059091-43059091 - ESO-224 COSM1269655 c.587C>T p.S196L Substitution - Missense 15:43070867-43070867 - 345973 COSM3726648 c.2678C>T p.T893I Substitution - Missense 15:43024890-43024890 - TCGA-BP-4176-01 COSM3361396 c.2392A>G p.T798A Substitution - Missense 15:43027816-43027816 - TCGA-BS-A0UF-01 COSM961876 c.1637T>G p.L546* Substitution - Nonsense 15:43047192-43047192 - PT49 COSM4054763 c.4528C>T p.R1510C Substitution - Missense 15:42966216-42966216 - TCGA-MU-A51Y-01 COSM4836566 c.1984G>A p.E662K Substitution - Missense 15:43037811-43037811 - LS180 COSM2187798 c.5122delC p.L1708fs*21 Deletion - Frameshift 15:42945457-42945457 - RMS109_ COSM4987052 c.16G>C p.A6P Substitution - Missense 15:43106007-43106007 - TCGA-22-4595-01 COSM700542 c.2812A>G p.T938A Substitution - Missense 15:43022729-43022729 - 2521249 COSM5888268 c.1648C>T p.Q550* Substitution - Nonsense 15:43047181-43047181 - T3094 COSM4738801 c.1861C>T p.R621C Substitution - Missense 15:43038221-43038221 - 3N36-VS-3T36 COSM4981172 c.4386G>T p.Q1462H Substitution - Missense 15:42970591-42970591 - TCGA-FD-A3SO-01 COSM3794177 c.3550C>T p.H1184Y Substitution - Missense 15:43002664-43002664 - Pat_41_B COSM5849204 c.463G>A p.E155K Substitution - Missense 15:43075044-43075044 - T70 COSM4054765 c.2680G>A p.V894I Substitution - Missense 15:43024888-43024888 - C658 COSM4054765 c.2680G>A p.V894I Substitution - Missense 15:43024888-43024888 - HCC2998 COSM4631599 c.402A>G p.K134K Substitution - coding silent 15:43082653-43082653 - LUAD-E00443 COSM363731 c.2887A>G p.K963E Substitution - Missense 15:43021328-43021328 - TCGA-G4-6588-01 COSM1372962 c.4117C>A p.L1373M Substitution - Missense 15:42983930-42983930 - CHC1754T COSM4792764 c.3451G>A p.A1151T Substitution - Missense 15:43003895-43003895 - SNU-283 COSM2187862 c.1539G>A p.Q513Q Substitution - coding silent 15:43048392-43048392 - TCGA-B8-4621-01 COSM470661 c.3209+1G>T p.? Unknown 15:43015687-43015687 - TCGA-A8-A092-01 COSM433887 c.3841G>A p.E1281K Substitution - Missense 15:42990037-42990037 - TCGA-FS-A1ZR-06 COSM2187863 c.1507C>T p.R503* Substitution - Nonsense 15:43048424-43048424 - Pat_41_B COSM5849201 c.1318G>A p.V440I Substitution - Missense 15:43054863-43054863 - pfg016T COSM1640243 c.1138_1139insT p.M380fs*18 Insertion - Frameshift 15:43058384-43058385 - ESCC-069T COSM3936757 c.2794G>A p.A932T Substitution - Missense 15:43022747-43022747 - sysucc-1507T COSM5766379 c.338+5G>A p.? Unknown 15:43085979-43085979 - YUVEME COSM5383340 c.3030T>C p.I1010I Substitution - coding silent 15:43015867-43015867 - 2492710 COSM2187797 c.5139G>A p.E1713E Substitution - coding silent 15:42945440-42945440 - TCGA-DD-A39Y-01 COSM4934526 c.2789A>G p.Q930R Substitution - Missense 15:43022752-43022752 - HCC066T COSM5821437 c.1450A>G p.I484V Substitution - Missense 15:43048481-43048481 - CSCC-11-T COSM4521223 c.10G>A p.E4K Substitution - Missense 15:43106013-43106013 - YUGAFFE COSM1708068 c.542C>T p.P181L Substitution - Missense 15:43070912-43070912 - TCGA-F5-6814-01 COSM3420309 c.473A>C p.K158T Substitution - Missense 15:43075034-43075034 - TCGA-AZ-4615-01 COSM3690403 c.904G>A p.V302I Substitution - Missense 15:43059783-43059783 - TCGA-BR-6452-01 COSM2187887 c.469T>C p.W157R Substitution - Missense 15:43075038-43075038 - 587222 COSM1231606 c.5152C>T p.L1718F Substitution - Missense 15:42945427-42945427 - 587376 COSM1231608 c.2368T>G p.L790V Substitution - Missense 15:43029955-43029955 - Pat_14_B COSM5849200 c.1951C>T p.R651C Substitution - Missense 15:43037844-43037844 - TCGA-DA-A1I5-06 COSM3501347 c.589G>A p.V197M Substitution - Missense 15:43070865-43070865 - TCGA-CG-5721-01 COSM4054763 c.4528C>T p.R1510C Substitution - Missense 15:42966216-42966216 - sysucc-311T COSM5478880 c.3154T>C p.Y1052H Substitution - Missense 15:43015743-43015743 - B59-Tumor COSM1756900 c.1510T>C p.S504P Substitution - Missense 15:43048421-43048421 - TCGA-GN-A26C-01 COSM3501339 c.3147A>G p.K1049K Substitution - coding silent 15:43015750-43015750 - 255 COSM3731857 c.1849+8T>C p.? Unknown 15:43043207-43043207 - 2492720 COSM5724190 c.4245C>T p.S1415S Substitution - coding silent 15:42976841-42976841 - HCT-15 COSM1678396 c.2257G>T p.E753* Substitution - Nonsense 15:43030066-43030066 - SC_9047 COSM5570771 c.4874T>C p.V1625A Substitution - Missense 15:42952410-42952410 - TCGA-06-6390 COSM2153434 c.2570A>G p.E857G Substitution - Missense 15:43025395-43025395 - TCGA-EE-A3JD-06 COSM4397136 c.4254G>A p.W1418* Substitution - Nonsense 15:42976832-42976832 - TCGA-EJ-7784-01 COSM1470819 c.5026G>C p.V1676L Substitution - Missense 15:42950344-42950344 - Pat_58_A COSM5849203 c.806G>A p.R269Q Substitution - Missense 15:43060107-43060107 - YUKAT COSM5383338 c.4050G>A p.R1350R Substitution - coding silent 15:42984890-42984890 - ATL059 COSM5705875 c.40A>T p.I14F Substitution - Missense 15:43105983-43105983 - ATL058 COSM5705874 c.3586C>A p.L1196I Substitution - Missense 15:43002628-43002628 - B105-Tumor COSM1756899 c.4415C>T p.S1472F Substitution - Missense 15:42970562-42970562 - SNU-C4 COSM4615557 c.4745delA p.N1582fs*13 Deletion - Frameshift 15:42960657-42960657 - CHEWS002 COSM165380 c.4659C>T p.L1553L Substitution - coding silent 15:42963976-42963976 - ESCC_143 COSM2187873 c.1137delT p.F379fs*15 Deletion - Frameshift 15:43058386-43058386 - 425 COSM4432712 c.49G>A p.E17K Substitution - Missense 15:43105974-43105974 - PD3890a COSM3664753 c.4460C>A p.S1487Y Substitution - Missense 15:42966284-42966284 - YUPAT COSM1708069 c.471G>A p.W157* Substitution - Nonsense 15:43075036-43075036 - B59 COSM1756900 c.1510T>C p.S504P Substitution - Missense 15:43048421-43048421 - TCGA-D1-A17Q-01 COSM961870 c.2722G>A p.E908K Substitution - Missense 15:43024846-43024846 - TCGA-EE-A29V-06 COSM3501348 c.480C>T p.G160G Substitution - coding silent 15:43075027-43075027 - RK169_C01 COSM3700958 c.3694C>G p.L1232V Substitution - Missense 15:42998231-42998231 - CCK81 COSM2187866 c.1451T>C p.I484T Substitution - Missense 15:43048480-43048480 - TCGA-Q1-A73P-01 COSM4825884 c.4204C>T p.L1402L Substitution - coding silent 15:42977894-42977894 - TCGA-C8-A26Y-01 COSM3816106 c.4259A>T p.D1420V Substitution - Missense 15:42976827-42976827 - TCGA-EE-A2GJ-06 COSM3501346 c.785C>G p.A262G Substitution - Missense 15:43067911-43067911 - TCGA-AX-A05Z-01 COSM961864 c.4010G>A p.G1337E Substitution - Missense 15:42984930-42984930 - Gp5D COSM2187808 c.4709C>T p.A1570V Substitution - Missense 15:42960693-42960693 - S00944 COSM316338 c.2575A>G p.K859E Substitution - Missense 15:43025390-43025390 - RKO COSM2187816 c.4242A>G p.P1414P Substitution - coding silent 15:42976844-42976844 - TCGA-CF-A1HS-01 COSM416930 c.1555C>T p.R519* Substitution - Nonsense 15:43047274-43047274 - S02139 COSM5674179 c.1600G>A p.A534T Substitution - Missense 15:43047229-43047229 - CSCC-19-T COSM4474831 c.1946C>T p.P649L Substitution - Missense 15:43037849-43037849 - HCT-15 COSM1678395 c.2258A>T p.E753V Substitution - Missense 15:43030065-43030065 - S00944 COSM316338 c.2575A>G p.K859E Substitution - Missense 15:43025390-43025390 - TCGA-33-6737-01 COSM700546 c.4411C>T p.H1471Y Substitution - Missense 15:42970566-42970566 - 1257T COSM5762556 c.2080A>G p.M694V Substitution - Missense 15:43036536-43036536 - TCGA-33-6737-01 COSM700543 c.2899C>T p.Q967* Substitution - Nonsense 15:43021316-43021316 - TCGA-AP-A051-01 COSM961863 c.4794T>C p.P1598P Substitution - coding silent 15:42958054-42958054 - 1N56-VS-1T56 COSM4977183 c.1932A>G p.V644V Substitution - coding silent 15:43037863-43037863 - S00936 COSM316337 c.4409C>T p.A1470V Substitution - Missense 15:42970568-42970568 - TCGA-56-6546-01 COSM700544 c.3960G>T p.L1320L Substitution - coding silent 15:42988856-42988856 - CHC892T COSM4960476 c.995G>A p.R332K Substitution - Missense 15:43059183-43059183 - HCC109T COSM5816791 c.4926G>T p.Q1642H Substitution - Missense 15:42952358-42952358 - ESO-049 COSM1269653 c.660-8_660-7insT p.? Unknown 15:43068043-43068044 - T3094 COSM961870 c.2722G>A p.E908K Substitution - Missense 15:43024846-43024846 - Capan-1 COSM328350 c.264G>A p.E88E Substitution - coding silent 15:43086058-43086058 - HCT8 COSM2187892 c.183G>A p.K61K Substitution - coding silent 15:43086139-43086139 - TCGA-A3-3376-01 COSM470662 c.2574C>G p.N858K Substitution - Missense 15:43025391-43025391 - TCGA-18-3419-01 COSM700538 c.437G>T p.G146V Substitution - Missense 15:43075070-43075070 - SNU-C4 COSM4652599 c.4166T>C p.I1389T Substitution - Missense 15:42977932-42977932 - T3118 COSM4738797 c.3694C>A p.L1232M Substitution - Missense 15:42998231-42998231 - ESO-0061 COSM1269654 c.1459C>A p.P487T Substitution - Missense 15:43048472-43048472 - HCC2998 COSM1678397 c.1552A>C p.I518L Substitution - Missense 15:43047277-43047277 - TCGA-FS-A1ZA-06 COSM3501335 c.4966C>T p.H1656Y Substitution - Missense 15:42952318-42952318 - 507 COSM5611925 c.2261G>C p.R754P Substitution - Missense 15:43030062-43030062 - CSCC-27-T COSM4566015 c.2898_2899CC>TT p.Q967* Substitution - Nonsense 15:43021316-43021317 - TCGA-B0-5092-01 COSM470663 c.2344C>T p.P782S Substitution - Missense 15:43029979-43029979 - SW48 COSM2187881 c.717C>A p.D239E Substitution - Missense 15:43067979-43067979 - P-Thy015 COSM5095233 c.541C>A p.P181T Substitution - Missense 15:43070913-43070913 - TCGA-BR-7851-01 COSM4054767 c.211T>C p.F71L Substitution - Missense 15:43086111-43086111 - TCGA-A7-A4SF-01 COSM3816109 c.781A>G p.T261A Substitution - Missense 15:43067915-43067915 - TCGA-E2-A2P6-01 COSM3816111 c.628G>A p.E210K Substitution - Missense 15:43070826-43070826 - TCGA-DK-A1AC-01 COSM1301138 c.3167C>T p.S1056L Substitution - Missense 15:43015730-43015730 - TCGA-ER-A193-06 COSM3501337 c.4244C>T p.S1415F Substitution - Missense 15:42976842-42976842 - TCGA-B5-A11E-01 COSM961867 c.3496G>A p.V1166M Substitution - Missense 15:43003850-43003850 - TCGA-BG-A0VW-01 COSM961873 c.2083C>T p.L695F Substitution - Missense 15:43036533-43036533 - 19 COSM5747635 c.2963T>C p.L988S Substitution - Missense 15:43017159-43017159 - 145 COSM3735137 c.2896C>T p.P966S Substitution - Missense 15:43021319-43021319 - TCGA-CA-6717-01 COSM3690402 c.4766G>T p.R1589I Substitution - Missense 15:42958082-42958082 - TCGA-DA-A3F8-06 COSM1708068 c.542C>T p.P181L Substitution - Missense 15:43070912-43070912 - TCGA-E2-A108-01 COSM433886 c.4945G>C p.E1649Q Substitution - Missense 15:42952339-42952339 - TCGA-B5-A11E-01 COSM961871 c.2488G>T p.D830Y Substitution - Missense 15:43026608-43026608 - TC32 COSM4578257 c.1177G>A p.V393M Substitution - Missense 15:43058346-43058346 - TCGA-G7-6795-01 COSM3987957 c.3310G>A p.E1104K Substitution - Missense 15:43007184-43007184 - PDA_019 COSM4998976 c.5195C>T p.A1732V Substitution - Missense 15:42945384-42945384 - PT36 COSM5916462 c.5062C>T p.P1688S Substitution - Missense 15:42950308-42950308 - PT35 COSM5913721 c.247C>T p.P83S Substitution - Missense 15:43086075-43086075 - RK080_C01 COSM1629563 c.862-6T>A p.? Unknown 15:43059831-43059831 - RK175_C01 COSM3744612 c.134A>T p.Q45L Substitution - Missense 15:43086188-43086188 - CSCC-40-T COSM4450210 c.488delG p.C163fs*2 Deletion - Frameshift 15:43075019-43075019 - HCC2998 COSM2187864 c.1500A>C p.E500D Substitution - Missense 15:43048431-43048431 - TCGA-A4-7288-01 COSM3987958 c.3210-1G>T p.? Unknown 15:43007285-43007285 - ESO-251 COSM1269656 c.4418C>T p.A1473V Substitution - Missense 15:42970559-42970559 - CSCC-40-T COSM4571539 c.486T>C p.F162F Substitution - coding silent 15:43075021-43075021 - T2269 COSM4738798 c.3359T>C p.V1120A Substitution - Missense 15:43007135-43007135 - T2269 COSM4738803 c.1156A>C p.K386Q Substitution - Missense 15:43058367-43058367 - C658 COSM416930 c.1555C>T p.R519* Substitution - Nonsense 15:43047274-43047274 - YUHEF COSM1708066 c.3011C>T p.S1004F Substitution - Missense 15:43017111-43017111 - RKO COSM2187815 c.4371C>T p.G1457G Substitution - coding silent 15:42970606-42970606 - 2492723 COSM5724190 c.4245C>T p.S1415S Substitution - coding silent 15:42976841-42976841 - TCGA-DK-A2I1-01 COSM1301139 c.674G>C p.R225T Substitution - Missense 15:43068022-43068022 - TCGA-G4-6628-01 COSM1372964 c.3290C>T p.T1097M Substitution - Missense 15:43007204-43007204 - 2334194 COSM41444 c.3466A>G p.T1156A Substitution - Missense 15:43003880-43003880 - sysucc-1247T COSM5764613 c.2366A>C p.N789T Substitution - Missense 15:43029957-43029957 - TCGA-EJ-7314-01 COSM1470818 c.4417G>A p.A1473T Substitution - Missense 15:42970560-42970560 - TCGA-BR-8487-01 COSM4054766 c.903A>G p.E301E Substitution - coding silent 15:43059784-43059784 - TCGA-AK-3429-01 COSM470660 c.3239T>G p.I1080S Substitution - Missense 15:43007255-43007255 - HCC2998 COSM1678397 c.1552A>C p.I518L Substitution - Missense 15:43047277-43047277 - PT19_2 COSM5900316 c.4378C>T p.L1460F Substitution - Missense 15:42970599-42970599 - TCGA-R2-A69V-01 COSM4851221 c.1782A>G p.E594E Substitution - coding silent 15:43043282-43043282 - DLD1 COSM2187892 c.183G>A p.K61K Substitution - coding silent 15:43086139-43086139 - B80 COSM1749147 c.3616A>G p.T1206A Substitution - Missense 15:43002598-43002598 - TCGA-D1-A15X-01 COSM961866 c.3545G>A p.R1182H Substitution - Missense 15:43002669-43002669 - TCGA-33-6737-01 COSM700545 c.4384C>G p.Q1462E Substitution - Missense 15:42970593-42970593 - TCGA-AF-2689-01 COSM287720 c.3140C>G p.T1047S Substitution - Missense 15:43015757-43015757 - 585223 COSM324162 c.1745G>T p.S582I Substitution - Missense 15:43043319-43043319 - TCGA-BS-A0UV-01 COSM961879 c.970A>G p.I324V Substitution - Missense 15:43059717-43059717 - TCGA-EE-A3J4-06 COSM3887001 c.648A>T p.E216D Substitution - Missense 15:43070806-43070806 - TCGA-18-4721-01 COSM700540 c.634G>T p.E212* Substitution - Nonsense 15:43070820-43070820 - LUAD-S01315 COSM344351 c.4111C>G p.Q1371E Substitution - Missense 15:42983936-42983936 - 401 COSM4429591 c.443T>G p.F148C Substitution - Missense 15:43075064-43075064 - TCGA-CH-5771-01 COSM1129202 c.4139G>A p.R1380H Substitution - Missense 15:42983908-42983908 - ME002T COSM222291 c.4975C>T p.H1659Y Substitution - Missense 15:42952309-42952309 - ESCC_13 COSM5625144 c.1200G>A p.Q400Q Substitution - coding silent 15:43056425-43056425 - TCGA-AO-A0JB-01 COSM433888 c.1353G>T p.E451D Substitution - Missense 15:43054828-43054828 - TCGA-CJ-4913-01 COSM470659 c.3913G>T p.G1305* Substitution - Nonsense 15:42988903-42988903 - HCT15 COSM1678395 c.2258A>T p.E753V Substitution - Missense 15:43030065-43030065 - TCGA-EE-A29M-06 COSM3501343 c.1647C>T p.F549F Substitution - coding silent 15:43047182-43047182 - CSCC-44-T COSM4506585 c.723C>T p.V241V Substitution - coding silent 15:43067973-43067973 - TCGA-GL-A4EM-01 COSM3987959 c.88G>A p.D30N Substitution - Missense 15:43086234-43086234 - TCGA-B0-4818-01 COSM470664 c.748G>A p.D250N Substitution - Missense 15:43067948-43067948 - PR-09-5446 COSM248182 c.898G>A p.V300I Substitution - Missense 15:43059789-43059789 - sysucc-311T COSM5478881 c.192A>C p.E64D Substitution - Missense 15:43086130-43086130 - TCGA-D3-A1Q6-06 COSM3501338 c.3352G>A p.A1118T Substitution - Missense 15:43007142-43007142 - TCGA-AX-A05Z-01 COSM961874 c.2071G>T p.D691Y Substitution - Missense 15:43036545-43036545 - TCGA-EW-A1J5-01 COSM1478130 c.3870C>G p.I1290M Substitution - Missense 15:42988946-42988946 - RK190_C01 COSM3744611 c.989A>T p.D330V Substitution - Missense 15:43059189-43059189 - PD3890a COSM3664753 c.4460C>A p.S1487Y Substitution - Missense 15:42966284-42966284 - TCGA-AX-A0J0-01 COSM961869 c.3043G>T p.E1015* Substitution - Nonsense 15:43015854-43015854 - YUKLAB COSM1708065 c.3088C>T p.R1030C Substitution - Missense 15:43015809-43015809 - UM-SCC-2 COSM3678189 c.4077G>A p.M1359I Substitution - Missense 15:42983970-42983970 - TCGA-AA-3715-01 COSM270496 c.2855C>T p.A952V Substitution - Missense 15:43021360-43021360 - HCT15 COSM1678396 c.2257G>T p.E753* Substitution - Nonsense 15:43030066-43030066 - TCGA-BS-A0UF-01 COSM961878 c.1314C>A p.I438I Substitution - coding silent 15:43054867-43054867 - TCGA-ED-A4XI-01 COSM4913218 c.2435A>C p.K812T Substitution - Missense 15:43026661-43026661 - TCGA-AX-A0J0-01 COSM961865 c.3780C>A p.F1260L Substitution - Missense 15:42990098-42990098 - T3024 COSM4738799 c.3337G>C p.A1113P Substitution - Missense 15:43007157-43007157 - TCGA-EE-A29E-06 COSM3501343 c.1647C>T p.F549F Substitution - coding silent 15:43047182-43047182 - SNUH_G76_S1 COSM4419640 c.5205A>G p.Q1735Q Substitution - coding silent 15:42945374-42945374 - C0062T COSM4150944 c.421C>A p.H141N Substitution - Missense 15:43075086-43075086 - LC_C23 COSM1188989 c.98T>A p.V33D Substitution - Missense 15:43086224-43086224 - B80-Tumor COSM1749147 c.3616A>G p.T1206A Substitution - Missense 15:43002598-43002598 - PACA46 COSM1158203 c.3888C>A p.L1296L Substitution - coding silent 15:42988928-42988928 - 1604875 COSM141450 c.1099C>T p.R367C Substitution - Missense 15:43058424-43058424 - TCGA-EE-A29L-06 COSM3501344 c.1589C>T p.P530L Substitution - Missense 15:43047240-43047240 - CHC1754T COSM4792764 c.3451G>A p.A1151T Substitution - Missense 15:43003895-43003895 - HN_00761 COSM130048 c.700G>C p.E234Q Substitution - Missense 15:43067996-43067996 - ME049T COSM230301 c.3860C>T p.S1287L Substitution - Missense 15:42988956-42988956 - TCGA-CG-5721-01 COSM4054762 c.4969G>A p.A1657T Substitution - Missense 15:42952315-42952315 - TCGA-BR-8687-01 COSM4054764 c.3095A>C p.K1032T Substitution - Missense 15:43015802-43015802 - TCGA-39-5036-01 COSM700539 c.534A>T p.S178S Substitution - coding silent 15:43070920-43070920 - B105 COSM1756899 c.4415C>T p.S1472F Substitution - Missense 15:42970562-42970562 - LAU618 COSM233702 c.4562G>T p.G1521V Substitution - Missense 15:42966182-42966182 - TCGA-E2-A2P6-01 COSM3816110 c.634G>A p.E212K Substitution - Missense 15:43070820-43070820 - TCGA-D3-A2JO-06 COSM3501341 c.2727G>A p.G909G Substitution - coding silent 15:43024841-43024841 - B80-3-Tumor COSM1749146 c.4548C>G p.F1516L Substitution - Missense 15:42966196-42966196 - BK0051 COSM4188049 c.2832G>C p.K944N Substitution - Missense 15:43022709-43022709 - QC2-32-T2 COSM4419640 c.5205A>G p.Q1735Q Substitution - coding silent 15:42945374-42945374 - GC_343T-GC_343N_a COSM4772387 c.2781A>G p.Q927Q Substitution - coding silent 15:43022760-43022760 - LUAD-CHTN-MAD06-00668 COSM358925 c.165G>T p.M55I Substitution - Missense 15:43086157-43086157 - EW8 COSM2187848 c.2153C>A p.A718D Substitution - Missense 15:43036215-43036215 - YUGURT COSM5383339 c.4027C>T p.L1343L Substitution - coding silent 15:42984913-42984913 - LUAD-B02594 COSM336478 c.1862G>T p.R621L Substitution - Missense 15:43038220-43038220 - TCGA-DK-A3WW-01 COSM3794176 c.3607C>T p.L1203L Substitution - coding silent 15:43002607-43002607 - 440 COSM4434401 c.3848+4A>G p.? Unknown 15:42990026-42990026 - 587376 COSM1231609 c.2056G>T p.E686* Substitution - Nonsense 15:43036560-43036560 - TCGA-EK-A3GK-01 COSM4853808 c.2011C>G p.L671V Substitution - Missense 15:43037784-43037784 - TCGA-AX-A05Z-01 COSM170963 c.1508G>A p.R503Q Substitution - Missense 15:43048423-43048423 - TCGA-EE-A2MN-06 COSM3501334 c.5001C>T p.F1667F Substitution - coding silent 15:42952283-42952283 - TCGA-D1-A103-01 COSM961872 c.2217A>G p.L739L Substitution - coding silent 15:43032605-43032605 - ESCC_53 COSM5631270 c.2094T>C p.G698G Substitution - coding silent 15:43036274-43036274 - CHC892T COSM4795602 c.1872G>A p.R624R Substitution - coding silent 15:43038210-43038210 - TCGA-G2-A2EO-01 COSM1301137 c.3918G>C p.L1306F Substitution - Missense 15:42988898-42988898 - TCGA-EE-A2M5-06 COSM3501342 c.2535G>A p.K845K Substitution - coding silent 15:43026561-43026561 - TCGA-AP-A056-01 COSM961868 c.3184G>T p.E1062* Substitution - Nonsense 15:43015713-43015713 - TCGA-87-5896-01 COSM3401739 c.4256A>T p.D1419V Substitution - Missense 15:42976830-42976830 - ccRCC-92 COSM1664863 c.4073T>A p.L1358* Substitution - Nonsense 15:42983974-42983974 - TCGA-FW-A3R5-06 COSM3887000 c.956C>T p.S319F Substitution - Missense 15:43059731-43059731 - 2492721 COSM5724190 c.4245C>T p.S1415S Substitution - coding silent 15:42976841-42976841 - TCGA-A5-A0VQ-01 COSM961880 c.879C>T p.V293V Substitution - coding silent 15:43059808-43059808 - 587376 COSM1231607 c.5146C>T p.R1716W Substitution - Missense 15:42945433-42945433 - TCGA-FW-A3R5-06 COSM3886999 c.3350C>T p.S1117L Substitution - Missense 15:43007144-43007144 - TCGA-F4-6856-01 COSM1372967 c.447T>C p.C149C Substitution - coding silent 15:43075060-43075060 - TCGA-DO-A2HM-01 COSM3370171 c.1229G>C p.R410T Substitution - Missense 15:43056396-43056396 - DN1307F COSM5962435 c.3740A>G p.N1247S Substitution - Missense 15:42998185-42998185 - sysucc-743T COSM5450994 c.3150C>T p.L1050L Substitution - coding silent 15:43015747-43015747 - ESO-859 COSM1240599 c.1993C>T p.R665* Substitution - Nonsense 15:43037802-43037802 - T272 COSM4738804 c.763G>A p.E255K Substitution - Missense 15:43067933-43067933 - 2492722 COSM5724190 c.4245C>T p.S1415S Substitution - coding silent 15:42976841-42976841 - LUAD-5V8LT COSM401544 c.4481G>T p.G1494V Substitution - Missense 15:42966263-42966263 - TCGA-CM-6171-01 COSM1372965 c.1778T>C p.L593S Substitution - Missense 15:43043286-43043286 - LC_C27 COSM1188987 c.4345C>G p.Q1449E Substitution - Missense 15:42976741-42976741 - 53M COSM5595530 c.5125C>T p.H1709Y Substitution - Missense 15:42945454-42945454 - HN_62532 COSM130047 c.3998A>G p.E1333G Substitution - Missense 15:42984942-42984942 - PT33 COSM5909477 c.2690G>A p.R897Q Substitution - Missense 15:43024878-43024878 - ESCC-078T COSM3936758 c.1253C>G p.S418* Substitution - Nonsense 15:43056372-43056372 - TCGA-AN-A046-01 COSM3816108 c.1204G>T p.E402* Substitution - Nonsense 15:43056421-43056421 - 61 COSM5740312 c.1868G>A p.S623N Substitution - Missense 15:43038214-43038214 - UM-SCC-17B COSM4598329 c.2888A>G p.K963R Substitution - Missense 15:43021327-43021327 - T3262 COSM4738802 c.1684G>A p.V562M Substitution - Missense 15:43043380-43043380 - 13280 COSM5616813 c.4370-3C>T p.? Unknown 15:42970610-42970610 - CSCC-55-T COSM4547915 c.4347G>A p.Q1449Q Substitution - coding silent 15:42976739-42976739 - T2269 COSM4738800 c.2311G>T p.E771* Substitution - Nonsense 15:43030012-43030012 - TCGA-AZ-4315-01 COSM1372968 c.365T>C p.V122A Substitution - Missense 15:43082690-43082690 - TCGA-AX-A06L-01 COSM961875 c.2018G>T p.S673I Substitution - Missense 15:43037777-43037777 - HCC2998 COSM2187843 c.2572A>C p.N858H Substitution - Missense 15:43025393-43025393 - D-13 COSM4766893 c.3490C>T p.H1164Y Substitution - Missense 15:43003856-43003856 - TCGA-EB-A41A-01 COSM1756899 c.4415C>T p.S1472F Substitution - Missense 15:42970562-42970562 - TCGA-D9-A1JW-06 COSM3501340 c.2827C>T p.H943Y Substitution - Missense 15:43022714-43022714 - TCGA-C8-A26Y-01 COSM3816107 c.4258G>A p.D1420N Substitution - Missense 15:42976828-42976828 - PT36 COSM5916463 c.4442C>T p.S1481F Substitution - Missense 15:42970535-42970535 - NCI-H209 COSM41444 c.3466A>G p.T1156A Substitution - Missense 15:43003880-43003880 - TCGA-EI-6917-01 COSM3420308 c.3873G>T p.K1291N Substitution - Missense 15:42988943-42988943 - TCGA-BS-A0UJ-01 COSM961862 c.5195C>A p.A1732D Substitution - Missense 15:42945384-42945384 - S0049 COSM5882572 c.152A>C p.Y51S Substitution - Missense 15:43086170-43086170 - TCGA-AK-3460-01 COSM3361397 c.476C>G p.T159S Substitution - Missense 15:43075031-43075031 - TCGA-A3-3363-01 COSM1493442 c.2689C>T p.R897W Substitution - Missense 15:43024879-43024879 - HCC32T COSM1608385 c.1282-9A>T p.? Unknown 15:43054908-43054908 - HCC32 COSM1608385 c.1282-9A>T p.? Unknown 15:43054908-43054908 - T3202 COSM4738805 c.343T>C p.C115R Substitution - Missense 15:43082712-43082712 - Pat_41_B COSM5849202 c.889C>T p.P297S Substitution - Missense 15:43059798-43059798 - ESCC_44 COSM5630010 c.3366A>G p.K1122K Substitution - coding silent 15:43007128-43007128 - PD4203a COSM165380 c.4659C>T p.L1553L Substitution - coding silent 15:42963976-42963976 - HCA7 COSM2187807 c.4745_4746insA p.N1582fs*8 Insertion - Frameshift 15:42960656-42960657 - TCGA-BR-A4QL-01 COSM4054761 c.5190G>A p.E1730E Substitution - coding silent 15:42945389-42945389 - C0008T COSM4150943 c.1587T>C p.D529D Substitution - coding silent 15:43047242-43047242 - 8044826 COSM1158203 c.3888C>A p.L1296L Substitution - coding silent 15:42988928-42988928 - HCT15 COSM2187892 c.183G>A p.K61K Substitution - coding silent 15:43086139-43086139 - Au1 COSM5597833 c.2746C>T p.H916Y Substitution - Missense 15:43022795-43022795 - YUKAT COSM5383341 c.1829C>T p.P610L Substitution - Missense 15:43043235-43043235 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.591121 15q13 605981

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.I1080S c.3239T>G 15 43299453 RCCC - A Frameshift p.M380Yfs*18 c.1137dupT 15 43350585 STAD A - Frameshift p.Q713Rfs*20 c.2136delT 15 43328430 CM - A SpliceDonorInsertion . c.4218+2dupT 15 43270076 THCA A T IntronicSNV . c.2536-8T>A 15 43317635 CM A T Missense p.F810I c.2428T>A 15 43319978 CM C A IntronicSNV . c.2536-40G>T 15 43317667 NSCLC C A Missense p.E451D c.1353G>T 15 43347026 BRCA C A Missense p.G146V c.437G>T 15 43367268 LUSC C A Missense p.G1647W c.4939G>T 15 43244543 LUAD C A Missense p.S582I c.1745G>T 15 43335517 SCLC C A Missense p.S673I c.2018G>T 15 43329975 UCEC C A Missense p.V419F c.1255G>T 15 43348568 LUAD C A Nonsense p.E212* c.634G>T 15 43363018 LUSC C A Nonsense p.G1305* c.3913G>T 15 43281101 RCCC C A SpliceDonorSNV . c.3209+1G>T 15 43307885 RCCC C A Synonymous p.L1320L c.3960G>T 15 43281054 LUSC CC AT Missense p.G1705I c.5113_5114delinsAT 15 43237663 CM C G Missense p.E1649Q c.4945G>C 15 43244537 BRCA C G Missense p.E234Q c.700G>C 15 43360194 HNSC C G Missense p.E301Q c.901G>C 15 43351984 HNSC C G Missense p.L1306F c.3918G>C 15 43281096 BLCA C G Missense p.Q1449H c.4347G>C 15 43268937 LUAD C G Missense p.R225T c.674G>C 15 43360220 BLCA C G Missense p.R410T c.1229G>C 15 43348594 THCA C G Missense p.V1676L c.5026G>C 15 43242542 PRAD C T 3-UTRSNV . c.5247+161G>A 15 43237369 CM C T IntronicSNV . c.3209+1749G>A 15 43306137 CLL C T Missense p.A1118T c.3352G>A 15 43299340 CM C T Missense p.A1473T c.4417G>A 15 43262758 PRAD C T Missense p.D1314N c.3940G>A 15 43281074 STAD C T Missense p.D250N c.748G>A 15 43360146 RCCC C T Missense p.E1281K c.3841G>A 15 43282235 BRCA C T Missense p.R1182H c.3545G>A 15 43294867 STAD C T Missense p.R1380H c.4139G>A 15 43276106 PRAD C T Missense p.V197M c.589G>A 15 43363063 CM C T Missense p.V241I c.721G>A 15 43360173 HNSC C T Nonsense p.W1418* c.4254G>A 15 43269030 CM C T Synonymous p.G909G c.2727G>A 15 43317039 CM C T Synonymous p.K507K c.1521G>A 15 43340608 CM C T Synonymous p.K845K c.2535G>A 15 43318759 CM G A IntronicSNV . c.4370-3C>T 15 43262808 NSCLC G A Missense p.A1470V c.4409C>T 15 43262766 SCLC G A Missense p.A1473V c.4418C>T 15 43262757 ESCA G A Missense p.H1471Y c.4411C>T 15 43262764 LUSC G A Missense p.H1656Y c.4966C>T 15 43244516 CM G A Missense p.H1659Y c.4975C>T 15 43244507 CM G A Missense p.H943Y c.2827C>T 15 43314912 CM G A Missense p.L695F c.2083C>T 15 43328731 UCEC G A Missense p.P1507L c.4520C>T 15 43258422 LUAD G A Missense p.P181L c.542C>T 15 43363110 CM G A Missense p.P297L c.890C>T 15 43351995 CM G A Missense p.P530L c.1589C>T 15 43339438 CM G A Missense p.R651C c.1951C>T 15 43330042 HNSC G A Missense p.S1287L c.3860C>T 15 43281154 CM G A Missense p.S1415F c.4244C>T 15 43269040 CM G A Missense p.S196L c.587C>T 15 43363065 ESCA G A Nonsense p.Q967* c.2899C>T 15 43313514 LUSC G A Nonsense p.R503* c.1507C>T 15 43340622 CM G A Nonsense p.R519* c.1555C>T 15 43339472 BLCA G A Nonsense p.R665* c.1993C>T 15 43330000 ESCA G A Synonymous p.A1686A c.5058C>T 15 43242510 CM G A Synonymous p.F1260F c.3780C>T 15 43282296 CM G A Synonymous p.F1667F c.5001C>T 15 43244481 CM G A Synonymous p.F549F c.1647C>T 15 43339380 CM G A Synonymous p.G160G c.480C>T 15 43367225 CM G A Synonymous p.L1553L c.4659C>T 15 43256174 BRCA G A Synonymous p.S1323S c.3969C>T 15 43281045 LUAD G A Synonymous p.S1432S c.4296C>T 15 43268988 CM G A Synonymous p.V293V c.879C>T 15 43352006 UCEC G C Missense p.A1227G c.3680C>G 15 43290443 STAD G C Missense p.A262G c.785C>G 15 43360109 CM G C Missense p.L1203V c.3607C>G 15 43294805 COREAD G C Missense p.N858K c.2574C>G 15 43317589 RCCC G C Missense p.Q1036E c.3106C>G 15 43307989 BRCA G C Missense p.Q1462E c.4384C>G 15 43262791 LUSC G C Missense p.Q967E c.2899C>G 15 43313514 CM G C Missense p.T1047S c.3140C>G 15 43307955 COREAD G C Missense p.T159S c.476C>G 15 43367229 RCCC G C Synonymous p.L962L c.2886C>G 15 43313527 LUAD G T Missense p.H837N c.2509C>A 15 43318785 CM G T Missense p.P487T c.1459C>A 15 43340670 ESCA T A Missense p.D1419V c.4256A>T 15 43269028 GBM T A Missense p.E216D c.648A>T 15 43363004 CM T A Missense p.Q1580L c.4739A>T 15 43252861 LUAD T A Missense p.Q466L c.1397A>T 15 43346982 HNSC T A Synonymous p.S178S c.534A>T 15 43363118 LUSC T C Missense p.E1333G c.3998A>G 15 43277140 HNSC T C Missense p.E857G c.2570A>G 15 43317593 GBM T C Missense p.K1390E c.4168A>G 15 43270128 COREAD T C Missense p.K859E c.2575A>G 15 43317588 SCLC T C Missense p.T1156A c.3466A>G 15 43296078 SCLC T C Missense p.T798A c.2392A>G 15 43320014 RCCC T C Missense p.T938A c.2812A>G 15 43314927 LUSC T C Synonymous p.K1049K c.3147A>G 15 43307948 CM - T Frameshift p.N1582Kfs*8 c.4745dupA 15 43252855 STAD