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 | 31776739 | 31776739 | + | Silent | SNP | C | C | G | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr15:31776739C>G | c.1539G>C | c.(1537-1539)gtG>gtC | p.V513V |
BLCA | 15 | 31776332 | 31776332 | + | Missense_Mutation | SNP | A | A | G | TCGA-FJ-A3ZE-01A-11D-A23M-08 | TCGA-FJ-A3ZE-10A-01D-A23K-08 | g.chr15:31776332A>G | c.1946T>C | c.(1945-1947)tTc>tCc | p.F649S |
BLCA | 15 | 31776455 | 31776455 | + | Missense_Mutation | SNP | C | C | T | TCGA-C4-A0F6-01A-11D-A10S-08 | TCGA-C4-A0F6-10A-01D-A10S-08 | g.chr15:31776455C>T | c.1823G>A | c.(1822-1824)cGg>cAg | p.R608Q |
BLCA | 15 | 31793915 | 31793915 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A3SR-01A-11D-A22Z-08 | TCGA-FD-A3SR-10A-01D-A22Z-08 | g.chr15:31793915C>G | c.1128G>C | c.(1126-1128)caG>caC | p.Q376H |
BLCA | 15 | 31795993 | 31795993 | + | Missense_Mutation | SNP | C | C | T | TCGA-BL-A0C8-01A-11D-A10S-08 | TCGA-BL-A0C8-10A-01D-A10S-08 | g.chr15:31795993C>T | c.901G>A | c.(901-903)Gag>Aag | p.E301K |
BLCA | 15 | 31818621 | 31818621 | + | Missense_Mutation | SNP | G | G | A | TCGA-CF-A3MI-01A-11D-A20D-08 | TCGA-CF-A3MI-10A-01D-A20D-08 | g.chr15:31818621G>A | c.803C>T | c.(802-804)aCg>aTg | p.T268M |
BLCA | 15 | 31819389 | 31819389 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr15:31819389T>A | c.775A>T | c.(775-777)Aag>Tag | p.K259* |
BLCA | 15 | 31851205 | 31851205 | + | Missense_Mutation | SNP | C | C | G | TCGA-C4-A0EZ-01A-21D-A10S-08 | TCGA-C4-A0EZ-10A-01D-A10S-08 | g.chr15:31851205C>G | c.517G>C | c.(517-519)Gag>Cag | p.E173Q |
BLCA | 15 | 31851254 | 31851254 | + | Silent | SNP | C | C | T | TCGA-XF-AAMR-01A-31D-A42E-08 | TCGA-XF-AAMR-10A-01D-A42H-08 | g.chr15:31851254C>T | c.468G>A | c.(466-468)ctG>ctA | p.L156L |
BLCA | 15 | 31862286 | 31862286 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A20T-01A-11D-A14W-08 | TCGA-BT-A20T-11A-11D-A14W-08 | g.chr15:31862286C>T | c.266G>A | c.(265-267)cGa>cAa | p.R89Q |
BRCA | 15 | 31776558 | 31776558 | + | Missense_Mutation | SNP | C | C | T | TCGA-A7-A26G-01A-21D-A167-09 | TCGA-A7-A26G-10A-01D-A167-09 | g.chr15:31776558C>T | c.1720G>A | c.(1720-1722)Gag>Aag | p.E574K |
BRCA | 15 | 31776728 | 31776728 | + | Missense_Mutation | SNP | A | A | G | TCGA-D8-A1XK-01A-21D-A14K-09 | TCGA-D8-A1XK-10A-01D-A14K-09 | g.chr15:31776728A>G | c.1550T>C | c.(1549-1551)cTg>cCg | p.L517P |
BRCA | 15 | 31776741 | 31776741 | + | Missense_Mutation | SNP | C | C | T | TCGA-AO-A129-01A-21D-A10M-09 | TCGA-AO-A129-10A-01D-A10M-09 | g.chr15:31776741C>T | c.1537G>A | c.(1537-1539)Gtg>Atg | p.V513M |
BRCA | 15 | 31776839 | 31776839 | + | Missense_Mutation | SNP | G | G | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr15:31776839G>A | c.1439C>T | c.(1438-1440)tCg>tTg | p.S480L |
BRCA | 15 | 31779758 | 31779758 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-D8-A1XQ-01A-11D-A14K-09 | TCGA-D8-A1XQ-10A-01D-A14K-09 | g.chr15:31779758delG | c.1162delC | c.(1162-1164)ctgfs | p.L388fs |
BRCA | 15 | 31819475 | 31819475 | + | Missense_Mutation | SNP | C | C | T | TCGA-A7-A4SA-01A-11D-A25Q-09 | TCGA-A7-A4SA-10A-01D-A25Q-09 | g.chr15:31819475C>T | c.689G>A | c.(688-690)cGg>cAg | p.R230Q |
BRCA | 15 | 31822945 | 31822945 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A5EI-01A-11D-A27P-09 | TCGA-AC-A5EI-10A-01D-A27P-09 | g.chr15:31822945C>T | c.617G>A | c.(616-618)gGg>gAg | p.G206E |
BRCA | 15 | 31851321 | 31851321 | + | Missense_Mutation | SNP | G | G | A | TCGA-A8-A09M-01A-11W-A019-09 | TCGA-A8-A09M-10A-01W-A021-09 | g.chr15:31851321G>A | c.401C>T | c.(400-402)gCa>gTa | p.A134V |
BRCA | 15 | 31947336 | 31947336 | + | Silent | SNP | C | C | T | TCGA-AQ-A54O-01A-11D-A25Q-09 | TCGA-AQ-A54O-10A-01D-A25Q-09 | g.chr15:31947336C>T | c.114G>A | c.(112-114)acG>acA | p.T38T |
CESC | 15 | 31795972 | 31795972 | + | Missense_Mutation | SNP | C | C | T | TCGA-WL-A834-01A-11D-A351-09 | TCGA-WL-A834-10A-01D-A351-09 | g.chr15:31795972C>T | c.922G>A | c.(922-924)Gtt>Att | p.V308I |
CESC | 15 | 31851254 | 31851254 | + | Silent | SNP | C | C | T | TCGA-C5-A3HE-01A-21D-A22X-09 | TCGA-C5-A3HE-10A-01D-A22X-09 | g.chr15:31851254C>T | c.468G>A | c.(466-468)ctG>ctA | p.L156L |
CHOL | 15 | 31794022 | 31794022 | + | Missense_Mutation | SNP | C | C | T | TCGA-3X-AAVE-01A-11D-A417-09 | TCGA-3X-AAVE-10A-01D-A41A-09 | g.chr15:31794022C>T | c.1021G>A | c.(1021-1023)Gga>Aga | p.G341R |
COAD | 15 | 31776400 | 31776400 | + | Silent | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr15:31776400G>A | c.1878C>T | c.(1876-1878)cgC>cgT | p.R626R |
COAD | 15 | 31776402 | 31776402 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr15:31776402G>A | c.1876C>T | c.(1876-1878)Cgc>Tgc | p.R626C |
COAD | 15 | 31776458 | 31776458 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr15:31776458G>A | c.1820C>T | c.(1819-1821)cCg>cTg | p.P607L |
COAD | 15 | 31776490 | 31776490 | + | Silent | SNP | C | C | T | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr15:31776490C>T | c.1788G>A | c.(1786-1788)gcG>gcA | p.A596A |
COAD | 15 | 31776529 | 31776529 | + | Silent | SNP | C | C | T | TCGA-AA-3821-01A-01W-0995-10 | TCGA-AA-3821-10A-01W-0995-10 | g.chr15:31776529C>T | c.1749G>A | c.(1747-1749)ccG>ccA | p.P583P |
COAD | 15 | 31776529 | 31776529 | + | Silent | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr15:31776529C>T | c.1749G>A | c.(1747-1749)ccG>ccA | p.P583P |
COAD | 15 | 31776859 | 31776859 | + | Silent | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr15:31776859C>T | c.1419G>A | c.(1417-1419)tcG>tcA | p.S473S |
COAD | 15 | 31776899 | 31776899 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr15:31776899G>A | c.1379C>T | c.(1378-1380)aCg>aTg | p.T460M |
COAD | 15 | 31793950 | 31793950 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:31793950G>T | c.1093C>A | c.(1093-1095)Caa>Aaa | p.Q365K |
COAD | 15 | 31795898 | 31795898 | + | Silent | SNP | T | T | C | TCGA-CM-5864-01A-01D-1650-10 | TCGA-CM-5864-10A-01D-1650-10 | g.chr15:31795898T>C | c.996A>G | c.(994-996)ggA>ggG | p.G332G |
COAD | 15 | 31796001 | 31796001 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr15:31796001G>A | c.893C>T | c.(892-894)cCc>cTc | p.P298L |
COAD | 15 | 31819422 | 31819422 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr15:31819422G>A | c.742C>T | c.(742-744)Cgg>Tgg | p.R248W |
COAD | 15 | 31819495 | 31819495 | + | Silent | SNP | G | G | A | TCGA-CA-6716-01A-11D-1835-10 | TCGA-CA-6716-10A-01D-1835-10 | g.chr15:31819495G>A | c.669C>T | c.(667-669)caC>caT | p.H223H |
COAD | 15 | 31851346 | 31851346 | + | Missense_Mutation | SNP | C | C | T | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr15:31851346C>T | c.376G>A | c.(376-378)Gtc>Atc | p.V126I |
COAD | 15 | 31851385 | 31851385 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr15:31851385G>A | c.337C>T | c.(337-339)Cgg>Tgg | p.R113W |
COAD | 15 | 31862368 | 31862368 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr15:31862368C>T | c.184G>A | c.(184-186)Gac>Aac | p.D62N |
COADREAD | 15 | 31776400 | 31776400 | + | Silent | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr15:31776400G>A | c.1878C>T | c.(1876-1878)cgC>cgT | p.R626R |
COADREAD | 15 | 31776402 | 31776402 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr15:31776402G>A | c.1876C>T | c.(1876-1878)Cgc>Tgc | p.R626C |
COADREAD | 15 | 31776458 | 31776458 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr15:31776458G>A | c.1820C>T | c.(1819-1821)cCg>cTg | p.P607L |
COADREAD | 15 | 31776490 | 31776490 | + | Silent | SNP | C | C | T | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr15:31776490C>T | c.1788G>A | c.(1786-1788)gcG>gcA | p.A596A |
COADREAD | 15 | 31776529 | 31776529 | + | Silent | SNP | C | C | T | TCGA-AA-3821-01A-01W-0995-10 | TCGA-AA-3821-10A-01W-0995-10 | g.chr15:31776529C>T | c.1749G>A | c.(1747-1749)ccG>ccA | p.P583P |
COADREAD | 15 | 31776529 | 31776529 | + | Silent | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr15:31776529C>T | c.1749G>A | c.(1747-1749)ccG>ccA | p.P583P |
COADREAD | 15 | 31776859 | 31776859 | + | Silent | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr15:31776859C>T | c.1419G>A | c.(1417-1419)tcG>tcA | p.S473S |
COADREAD | 15 | 31776899 | 31776899 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr15:31776899G>A | c.1379C>T | c.(1378-1380)aCg>aTg | p.T460M |
COADREAD | 15 | 31793950 | 31793950 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:31793950G>T | c.1093C>A | c.(1093-1095)Caa>Aaa | p.Q365K |
COADREAD | 15 | 31795898 | 31795898 | + | Silent | SNP | T | T | C | TCGA-CM-5864-01A-01D-1650-10 | TCGA-CM-5864-10A-01D-1650-10 | g.chr15:31795898T>C | c.996A>G | c.(994-996)ggA>ggG | p.G332G |
COADREAD | 15 | 31796001 | 31796001 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr15:31796001G>A | c.893C>T | c.(892-894)cCc>cTc | p.P298L |
COADREAD | 15 | 31796012 | 31796012 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:31796012G>T | c.882C>A | c.(880-882)aaC>aaA | p.N294K |
COADREAD | 15 | 31819422 | 31819422 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr15:31819422G>A | c.742C>T | c.(742-744)Cgg>Tgg | p.R248W |
COADREAD | 15 | 31819495 | 31819495 | + | Silent | SNP | G | G | A | TCGA-CA-6716-01A-11D-1835-10 | TCGA-CA-6716-10A-01D-1835-10 | g.chr15:31819495G>A | c.669C>T | c.(667-669)caC>caT | p.H223H |
COADREAD | 15 | 31822970 | 31822970 | + | Missense_Mutation | SNP | G | G | A | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr15:31822970G>A | c.592C>T | c.(592-594)Cgg>Tgg | p.R198W |
COADREAD | 15 | 31851346 | 31851346 | + | Missense_Mutation | SNP | C | C | T | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr15:31851346C>T | c.376G>A | c.(376-378)Gtc>Atc | p.V126I |
COADREAD | 15 | 31851385 | 31851385 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr15:31851385G>A | c.337C>T | c.(337-339)Cgg>Tgg | p.R113W |
COADREAD | 15 | 31862368 | 31862368 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr15:31862368C>T | c.184G>A | c.(184-186)Gac>Aac | p.D62N |
DLBC | 15 | 31776837 | 31776837 | + | Missense_Mutation | SNP | C | C | G | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr15:31776837C>G | c.1441G>C | c.(1441-1443)Gtg>Ctg | p.V481L |
DLBC | 15 | 31776837 | 31776837 | + | Missense_Mutation | SNP | C | C | G | TCGA-G8-6914-01A-11D-2210-10 | TCGA-G8-6914-14A-01D-2210-10 | g.chr15:31776837C>G | c.1441G>C | c.(1441-1443)Gtg>Ctg | p.V481L |
ESCA | 15 | 31776544 | 31776544 | + | Silent | SNP | C | C | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr15:31776544C>A | c.1734G>T | c.(1732-1734)tcG>tcT | p.S578S |
ESCA | 15 | 31796012 | 31796012 | + | Missense_Mutation | SNP | G | G | T | TCGA-LN-A8I0-01A-11D-A36J-09 | TCGA-LN-A8I0-10A-01D-A36M-09 | g.chr15:31796012G>T | c.882C>A | c.(880-882)aaC>aaA | p.N294K |
ESCA | 15 | 31822940 | 31822940 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A7HZ-01A-31D-A351-09 | TCGA-LN-A7HZ-10A-01D-A351-09 | g.chr15:31822940C>T | c.622G>A | c.(622-624)Ggg>Agg | p.G208R |
GBM | 15 | 31776752 | 31776752 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-0789-01A-01W-0424-08 | TCGA-14-0789-10A-01W-0424-08 | g.chr15:31776752C>T | c.1526G>A | c.(1525-1527)cGc>cAc | p.R509H |
GBMLGG | 15 | 31776380 | 31776380 | + | Missense_Mutation | SNP | C | C | T | TCGA-HT-A4DS-01A-11D-A26M-08 | TCGA-HT-A4DS-10A-01D-A26K-08 | g.chr15:31776380C>T | c.1898G>A | c.(1897-1899)cGc>cAc | p.R633H |
GBMLGG | 15 | 31776752 | 31776752 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-0789-01A-01W-0424-08 | TCGA-14-0789-10A-01W-0424-08 | g.chr15:31776752C>T | c.1526G>A | c.(1525-1527)cGc>cAc | p.R509H |
GBMLGG | 15 | 31862287 | 31862287 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:31862287G>A | c.265C>T | c.(265-267)Cga>Tga | p.R89* |
HNSC | 15 | 31776457 | 31776457 | + | Silent | SNP | C | C | T | TCGA-DQ-7592-01A-11D-2078-08 | TCGA-DQ-7592-10A-01D-2078-08 | g.chr15:31776457C>T | c.1821G>A | c.(1819-1821)ccG>ccA | p.P607P |
HNSC | 15 | 31776545 | 31776545 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A6K2-01A-11D-A31L-08 | TCGA-CV-A6K2-10A-01D-A31J-08 | g.chr15:31776545G>A | c.1733C>T | c.(1732-1734)tCg>tTg | p.S578L |
HNSC | 15 | 31776656 | 31776656 | + | Missense_Mutation | SNP | C | C | T | TCGA-QK-A6VB-01A-12D-A34J-08 | TCGA-QK-A6VB-10B-01D-A34M-08 | g.chr15:31776656C>T | c.1622G>A | c.(1621-1623)gGc>gAc | p.G541D |
HNSC | 15 | 31818596 | 31818596 | + | Silent | SNP | G | G | A | TCGA-F7-A50J-01A-21D-A28R-08 | TCGA-F7-A50J-10A-01D-A28U-08 | g.chr15:31818596G>A | c.828C>T | c.(826-828)agC>agT | p.S276S |
HNSC | 15 | 31819495 | 31819495 | + | Missense_Mutation | SNP | G | G | C | TCGA-F7-7848-01A-11D-2129-08 | TCGA-F7-7848-10A-01D-2129-08 | g.chr15:31819495G>C | c.669C>G | c.(667-669)caC>caG | p.H223Q |
HNSC | 15 | 31947302 | 31947302 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CV-A45X-01A-21D-A25D-08 | TCGA-CV-A45X-10A-01D-A25E-08 | g.chr15:31947302C>A | c.148G>T | c.(148-150)Gaa>Taa | p.E50* |
KICH | 15 | 31779425 | 31779425 | + | Missense_Mutation | SNP | G | G | A | TCGA-KL-8329-01A-11D-2310-10 | TCGA-KL-8329-11A-01D-2310-10 | g.chr15:31779425G>A | c.1322C>T | c.(1321-1323)aCg>aTg | p.T441M |
KICH | 15 | 31779681 | 31779681 | + | Silent | SNP | G | G | A | TCGA-KL-8324-01A-11D-2310-10 | TCGA-KL-8324-11A-01D-2310-10 | g.chr15:31779681G>A | c.1239C>T | c.(1237-1239)gaC>gaT | p.D413D |
KIPAN | 15 | 31779425 | 31779425 | + | Missense_Mutation | SNP | G | G | A | TCGA-KL-8329-01A-11D-2310-10 | TCGA-KL-8329-11A-01D-2310-10 | g.chr15:31779425G>A | c.1322C>T | c.(1321-1323)aCg>aTg | p.T441M |
KIPAN | 15 | 31779681 | 31779681 | + | Silent | SNP | G | G | A | TCGA-KL-8324-01A-11D-2310-10 | TCGA-KL-8324-11A-01D-2310-10 | g.chr15:31779681G>A | c.1239C>T | c.(1237-1239)gaC>gaT | p.D413D |
KIPAN | 15 | 31818596 | 31818596 | + | Silent | SNP | G | G | A | TCGA-P4-A5E6-01A-11D-A28G-10 | TCGA-P4-A5E6-11A-22D-A28G-10 | g.chr15:31818596G>A | c.828C>T | c.(826-828)agC>agT | p.S276S |
KIRP | 15 | 31818596 | 31818596 | + | Silent | SNP | G | G | A | TCGA-P4-A5E6-01A-11D-A28G-10 | TCGA-P4-A5E6-11A-22D-A28G-10 | g.chr15:31818596G>A | c.828C>T | c.(826-828)agC>agT | p.S276S |
LGG | 15 | 31776380 | 31776380 | + | Missense_Mutation | SNP | C | C | T | TCGA-HT-A4DS-01A-11D-A26M-08 | TCGA-HT-A4DS-10A-01D-A26K-08 | g.chr15:31776380C>T | c.1898G>A | c.(1897-1899)cGc>cAc | p.R633H |
LGG | 15 | 31862287 | 31862287 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:31862287G>A | c.265C>T | c.(265-267)Cga>Tga | p.R89* |
LIHC | 15 | 31776404 | 31776404 | + | Missense_Mutation | SNP | A | A | C | TCGA-CC-A7IK-01A-12D-A33Q-10 | TCGA-CC-A7IK-10A-01D-A33Q-10 | g.chr15:31776404A>C | c.1874T>G | c.(1873-1875)cTg>cGg | p.L625R |
LIHC | 15 | 31776670 | 31776670 | + | Silent | SNP | G | G | A | TCGA-5R-AA1D-01A-11D-A382-10 | TCGA-5R-AA1D-10A-01D-A385-10 | g.chr15:31776670G>A | c.1608C>T | c.(1606-1608)ggC>ggT | p.G536G |
LUAD | 15 | 31776342 | 31776342 | + | Missense_Mutation | SNP | G | G | A | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr15:31776342G>A | c.1936C>T | c.(1936-1938)Cgg>Tgg | p.R646W |
LUAD | 15 | 31776389 | 31776389 | + | Missense_Mutation | SNP | T | T | A | TCGA-78-7539-01A-11D-2063-08 | TCGA-78-7539-10A-01D-2063-08 | g.chr15:31776389T>A | c.1889A>T | c.(1888-1890)cAg>cTg | p.Q630L |
LUAD | 15 | 31776661 | 31776661 | + | Silent | SNP | C | C | A | TCGA-53-A4EZ-01A-12D-A24P-08 | TCGA-53-A4EZ-10A-01D-A24P-08 | g.chr15:31776661C>A | c.1617G>T | c.(1615-1617)gtG>gtT | p.V539V |
LUAD | 15 | 31776742 | 31776742 | + | Silent | SNP | G | G | C | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr15:31776742G>C | c.1536C>G | c.(1534-1536)tcC>tcG | p.S512S |
LUAD | 15 | 31776743 | 31776743 | + | Missense_Mutation | SNP | G | G | T | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr15:31776743G>T | c.1535C>A | c.(1534-1536)tCc>tAc | p.S512Y |
LUAD | 15 | 31779707 | 31779707 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr15:31779707C>A | c.1213G>T | c.(1213-1215)Ggc>Tgc | p.G405C |
LUAD | 15 | 31779767 | 31779767 | + | Missense_Mutation | SNP | C | C | T | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr15:31779767C>T | c.1153G>A | c.(1153-1155)Gtg>Atg | p.V385M |
LUAD | 15 | 31796019 | 31796019 | + | Missense_Mutation | SNP | A | A | T | TCGA-55-5899-01A-11D-1625-08 | TCGA-55-5899-10A-01D-1625-08 | g.chr15:31796019A>T | c.875T>A | c.(874-876)gTg>gAg | p.V292E |
LUAD | 15 | 31818568 | 31818568 | + | Missense_Mutation | SNP | C | C | T | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr15:31818568C>T | c.856G>A | c.(856-858)Ggc>Agc | p.G286S |
LUAD | 15 | 31819434 | 31819434 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-8585-01A-11D-2393-08 | TCGA-86-8585-10A-01D-2393-08 | g.chr15:31819434C>T | c.730G>A | c.(730-732)Gaa>Aaa | p.E244K |
LUAD | 15 | 31819480 | 31819480 | + | Silent | SNP | C | C | A | TCGA-50-5072-01A-21D-1855-08 | TCGA-50-5072-10A-01D-1855-08 | g.chr15:31819480C>A | c.684G>T | c.(682-684)gtG>gtT | p.V228V |
LUAD | 15 | 31819488 | 31819488 | + | Missense_Mutation | SNP | C | C | T | TCGA-78-7156-01A-11D-2036-08 | TCGA-78-7156-10A-01D-2036-08 | g.chr15:31819488C>T | c.676G>A | c.(676-678)Gac>Aac | p.D226N |
LUAD | 15 | 31819497 | 31819497 | + | Missense_Mutation | SNP | G | G | C | TCGA-49-4514-01A-21D-1855-08 | TCGA-49-4514-11A-01D-1855-08 | g.chr15:31819497G>C | c.667C>G | c.(667-669)Cac>Gac | p.H223D |
LUAD | 15 | 31822943 | 31822943 | + | Missense_Mutation | SNP | C | C | A | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr15:31822943C>A | c.619G>T | c.(619-621)Gat>Tat | p.D207Y |
LUAD | 15 | 31851205 | 31851205 | + | Missense_Mutation | SNP | C | C | T | TCGA-49-4514-01A-21D-1855-08 | TCGA-49-4514-11A-01D-1855-08 | g.chr15:31851205C>T | c.517G>A | c.(517-519)Gag>Aag | p.E173K |
LUAD | 15 | 31851274 | 31851274 | + | Missense_Mutation | SNP | T | T | G | TCGA-44-8120-01A-11D-2238-08 | TCGA-44-8120-10A-01D-2238-08 | g.chr15:31851274T>G | c.448A>C | c.(448-450)Aca>Cca | p.T150P |
LUAD | 15 | 31862303 | 31862303 | + | Silent | SNP | A | A | G | TCGA-55-1592-01A-01D-0969-08 | TCGA-55-1592-11A-01D-0969-08 | g.chr15:31862303A>G | c.249T>C | c.(247-249)ggT>ggC | p.G83G |
LUAD | 15 | 31862369 | 31862369 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr15:31862369G>T | c.183C>A | c.(181-183)agC>agA | p.S61R |
LUAD | 15 | 31862380 | 31862380 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z045-01A-01W-0746-08 | TCGA-17-Z045-11A-01W-0747-08 | g.chr15:31862380C>A | c.172G>T | c.(172-174)Gcc>Tcc | p.A58S |
LUSC | 15 | 31776442 | 31776442 | + | Missense_Mutation | SNP | C | C | A | TCGA-34-5231-01A-21D-1817-08 | TCGA-34-5231-10A-01D-1817-08 | g.chr15:31776442C>A | c.1836G>T | c.(1834-1836)tgG>tgT | p.W612C |
LUSC | 15 | 31776570 | 31776570 | + | Missense_Mutation | SNP | C | C | A | TCGA-22-5485-01A-01D-1632-08 | TCGA-22-5485-11A-01D-1632-08 | g.chr15:31776570C>A | c.1708G>T | c.(1708-1710)Ggc>Tgc | p.G570C |
LUSC | 15 | 31776859 | 31776859 | + | Silent | SNP | C | C | A | TCGA-33-4532-01A-01D-1267-08 | TCGA-33-4532-11A-01D-1267-08 | g.chr15:31776859C>A | c.1419G>T | c.(1417-1419)tcG>tcT | p.S473S |
LUSC | 15 | 31862290 | 31862290 | + | Missense_Mutation | SNP | C | C | G | TCGA-22-5477-01A-01D-1632-08 | TCGA-22-5477-11A-11D-1632-08 | g.chr15:31862290C>G | c.262G>C | c.(262-264)Gag>Cag | p.E88Q |
PAAD | 15 | 31793994 | 31793994 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:31793994G>T | c.1049C>A | c.(1048-1050)cCt>cAt | p.P350H |
PAAD | 15 | 31818563 | 31818563 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:31818563G>A | c.861C>T | c.(859-861)ggC>ggT | p.G287G |
PAAD | 15 | 31822993 | 31822993 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:31822993G>T | c.569C>A | c.(568-570)tCc>tAc | p.S190Y |
PRAD | 15 | 31776773 | 31776773 | + | Missense_Mutation | SNP | C | C | T | TCGA-HC-7821-01A-12D-2114-08 | TCGA-HC-7821-10A-01D-2115-08 | g.chr15:31776773C>T | c.1505G>A | c.(1504-1506)cGc>cAc | p.R502H |
PRAD | 15 | 31851385 | 31851385 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr15:31851385G>A | c.337C>T | c.(337-339)Cgg>Tgg | p.R113W |
READ | 15 | 31796012 | 31796012 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:31796012G>T | c.882C>A | c.(880-882)aaC>aaA | p.N294K |
READ | 15 | 31822970 | 31822970 | + | Missense_Mutation | SNP | G | G | A | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr15:31822970G>A | c.592C>T | c.(592-594)Cgg>Tgg | p.R198W |
SARC | 15 | 31819495 | 31819495 | + | Silent | SNP | G | G | A | TCGA-DX-AB32-01A-11D-A417-09 | TCGA-DX-AB32-10A-01D-A41A-09 | g.chr15:31819495G>A | c.669C>T | c.(667-669)caC>caT | p.H223H |
SKCM | 15 | 31776364 | 31776364 | + | Silent | SNP | G | G | A | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr15:31776364G>A | c.1914C>T | c.(1912-1914)gcC>gcT | p.A638A |
SKCM | 15 | 31776365 | 31776365 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr15:31776365G>A | c.1913C>T | c.(1912-1914)gCc>gTc | p.A638V |
SKCM | 15 | 31776565 | 31776565 | + | Missense_Mutation | SNP | G | G | C | TCGA-FS-A1YW-06A-11D-A197-08 | TCGA-FS-A1YW-10A-01D-A199-08 | g.chr15:31776565G>C | c.1713C>G | c.(1711-1713)agC>agG | p.S571R |
SKCM | 15 | 31776795 | 31776795 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr15:31776795C>T | c.1483G>A | c.(1483-1485)Gac>Aac | p.D495N |
SKCM | 15 | 31779421 | 31779421 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FR-A3YO-06A-11D-A23B-08 | TCGA-FR-A3YO-10A-01D-A23B-08 | g.chr15:31779421C>T | c.1326G>A | c.(1324-1326)tgG>tgA | p.W442* |
SKCM | 15 | 31779660 | 31779660 | + | Silent | SNP | C | C | T | TCGA-EE-A17X-06A-11D-A197-08 | TCGA-EE-A17X-10A-01D-A199-08 | g.chr15:31779660C>T | c.1260G>A | c.(1258-1260)ctG>ctA | p.L420L |
SKCM | 15 | 31793901 | 31793901 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A148-06A-11D-A19A-08 | TCGA-D9-A148-10A-01D-A19A-08 | g.chr15:31793901C>T | c.1142G>A | c.(1141-1143)aGa>aAa | p.R381K |
SKCM | 15 | 31793992 | 31793992 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr15:31793992G>A | c.1051C>T | c.(1051-1053)Ccc>Tcc | p.P351S |
SKCM | 15 | 31795975 | 31795975 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr15:31795975G>A | c.919C>T | c.(919-921)Cac>Tac | p.H307Y |
SKCM | 15 | 31795993 | 31795993 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr15:31795993C>T | c.901G>A | c.(901-903)Gag>Aag | p.E301K |
SKCM | 15 | 31819474 | 31819474 | + | Silent | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr15:31819474C>T | c.690G>A | c.(688-690)cgG>cgA | p.R230R |
SKCM | 15 | 31819489 | 31819489 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr15:31819489C>T | c.675G>A | c.(673-675)cgG>cgA | p.R225R |
SKCM | 15 | 31822943 | 31822943 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr15:31822943C>T | c.619G>A | c.(619-621)Gat>Aat | p.D207N |
SKCM | 15 | 31822961 | 31822961 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3C8-06A-12D-A19A-08 | TCGA-D3-A3C8-10A-01D-A19A-08 | g.chr15:31822961G>A | c.601C>T | c.(601-603)Cct>Tct | p.P201S |
SKCM | 15 | 31822993 | 31822993 | + | Missense_Mutation | SNP | G | G | T | TCGA-FR-A44A-06A-11D-A24R-08 | TCGA-FR-A44A-10A-01D-A24R-08 | g.chr15:31822993G>T | c.569C>A | c.(568-570)tCc>tAc | p.S190Y |
SKCM | 15 | 31851206 | 31851206 | + | Silent | SNP | G | G | A | TCGA-EE-A3AF-06A-11D-A196-08 | TCGA-EE-A3AF-10A-01D-A198-08 | g.chr15:31851206G>A | c.516C>T | c.(514-516)atC>atT | p.I172I |
SKCM | 15 | 31851329 | 31851329 | + | Silent | SNP | G | G | A | TCGA-EE-A2M6-06A-12D-A197-08 | TCGA-EE-A2M6-10A-01D-A199-08 | g.chr15:31851329G>A | c.393C>T | c.(391-393)tcC>tcT | p.S131S |
SKCM | 15 | 31862347 | 31862347 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr15:31862347C>T | c.205G>A | c.(205-207)Gtg>Atg | p.V69M |
SKCM | 15 | 31862357 | 31862357 | + | Silent | SNP | C | C | T | TCGA-ER-A19L-06A-12D-A197-08 | TCGA-ER-A19L-10A-01D-A199-08 | g.chr15:31862357C>T | c.195G>A | c.(193-195)caG>caA | p.Q65Q |