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 | 1 | 233515177 | 233515177 | + | Missense_Mutation | SNP | A | A | T | TCGA-OR-A5KT-01A-11D-A29I-10 | TCGA-OR-A5KT-10A-01D-A29L-10 | g.chr1:233515177A>T | c.2425A>T | c.(2425-2427)Aca>Tca | p.T809S |
BLCA | 1 | 233464285 | 233464285 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A6MD-01A-41D-A34U-08 | TCGA-E7-A6MD-10B-01D-A34X-08 | g.chr1:233464285G>A | c.511G>A | c.(511-513)Gag>Aag | p.E171K |
BLCA | 1 | 233482330 | 233482330 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-AAML-01A-11D-A42E-08 | TCGA-XF-AAML-10A-01D-A42H-08 | g.chr1:233482330C>G | c.948C>G | c.(946-948)atC>atG | p.I316M |
BLCA | 1 | 233489599 | 233489599 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1A6-01A-11D-A13W-08 | TCGA-DK-A1A6-10A-01D-A13W-08 | g.chr1:233489599C>T | c.1033C>T | c.(1033-1035)Cgg>Tgg | p.R345W |
BLCA | 1 | 233497931 | 233497931 | + | Missense_Mutation | SNP | C | C | G | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr1:233497931C>G | c.1444C>G | c.(1444-1446)Ctg>Gtg | p.L482V |
BLCA | 1 | 233507842 | 233507842 | + | Silent | SNP | G | G | A | TCGA-DK-AA6S-01A-21D-A391-08 | TCGA-DK-AA6S-10A-01D-A394-08 | g.chr1:233507842G>A | c.1611G>A | c.(1609-1611)ctG>ctA | p.L537L |
BLCA | 1 | 233511790 | 233511790 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9T0-01A-11D-A391-08 | TCGA-XF-A9T0-10A-01D-A394-08 | g.chr1:233511790G>A | c.1804G>A | c.(1804-1806)Gat>Aat | p.D602N |
BLCA | 1 | 233512183 | 233512183 | + | Missense_Mutation | SNP | C | C | A | TCGA-FD-A3N5-01A-11D-A21A-08 | TCGA-FD-A3N5-10A-01D-A21A-08 | g.chr1:233512183C>A | c.1834C>A | c.(1834-1836)Cct>Act | p.P612T |
BLCA | 1 | 233515349 | 233515349 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-AAN7-01A-11D-A42E-08 | TCGA-XF-AAN7-10A-01D-A42H-08 | g.chr1:233515349C>T | c.2597C>T | c.(2596-2598)cCg>cTg | p.P866L |
BRCA | 1 | 233482294 | 233482294 | + | Silent | SNP | A | A | G | TCGA-E2-A1AZ-01A-11D-A12Q-09 | TCGA-E2-A1AZ-10A-01D-A12Q-09 | g.chr1:233482294A>G | c.912A>G | c.(910-912)acA>acG | p.T304T |
BRCA | 1 | 233490631 | 233490631 | + | Silent | SNP | C | C | A | TCGA-AR-A0TY-01A-12W-A12T-09 | TCGA-AR-A0TY-10A-01D-A110-09 | g.chr1:233490631C>A | c.1185C>A | c.(1183-1185)ctC>ctA | p.L395L |
BRCA | 1 | 233490734 | 233490734 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A2L8-01A-11D-A18P-09 | TCGA-BH-A2L8-10A-01D-A18P-09 | g.chr1:233490734G>A | c.1288G>A | c.(1288-1290)Gat>Aat | p.D430N |
BRCA | 1 | 233512266 | 233512266 | + | Silent | SNP | C | C | T | TCGA-A7-A3RF-01A-11D-A228-09 | TCGA-A7-A3RF-10A-01D-A22A-09 | g.chr1:233512266C>T | c.1917C>T | c.(1915-1917)gaC>gaT | p.D639D |
BRCA | 1 | 233515008 | 233515008 | + | Silent | SNP | G | G | A | TCGA-AN-A0AT-01A-11D-A045-09 | TCGA-AN-A0AT-10A-01W-A055-09 | g.chr1:233515008G>A | c.2256G>A | c.(2254-2256)ttG>ttA | p.L752L |
BRCA | 1 | 233515233 | 233515233 | + | Silent | SNP | C | C | G | TCGA-GM-A2D9-01A-11D-A18P-09 | TCGA-GM-A2D9-11A-42D-A18P-09 | g.chr1:233515233C>G | c.2481C>G | c.(2479-2481)gtC>gtG | p.V827V |
BRCA | 1 | 233518092 | 233518092 | + | Missense_Mutation | SNP | C | C | T | TCGA-EW-A1P4-01A-21D-A142-09 | TCGA-EW-A1P4-10A-01D-A142-09 | g.chr1:233518092C>T | c.2746C>T | c.(2746-2748)Cca>Tca | p.P916S |
BRCA | 1 | 233518401 | 233518401 | + | Missense_Mutation | SNP | A | A | G | TCGA-A8-A08Z-01A-21W-A019-09 | TCGA-A8-A08Z-10A-01W-A021-09 | g.chr1:233518401A>G | c.3055A>G | c.(3055-3057)Agg>Ggg | p.R1019G |
CESC | 1 | 233482309 | 233482309 | + | Silent | SNP | C | C | A | TCGA-EX-A69M-01A-11D-A32I-09 | TCGA-EX-A69M-10A-01D-A32I-09 | g.chr1:233482309C>A | c.927C>A | c.(925-927)gcC>gcA | p.A309A |
CESC | 1 | 233489616 | 233489616 | + | Silent | SNP | C | C | T | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chr1:233489616C>T | c.1050C>T | c.(1048-1050)ctC>ctT | p.L350L |
CESC | 1 | 233497990 | 233497990 | + | Missense_Mutation | SNP | G | G | C | TCGA-FU-A3HY-01A-11D-A21Q-09 | TCGA-FU-A3HY-10A-01D-A21Q-09 | g.chr1:233497990G>C | c.1503G>C | c.(1501-1503)aaG>aaC | p.K501N |
CESC | 1 | 233514845 | 233514845 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A7UH-01A-11D-A351-09 | TCGA-C5-A7UH-10A-01D-A351-09 | g.chr1:233514845C>T | c.2093C>T | c.(2092-2094)gCc>gTc | p.A698V |
CESC | 1 | 233518245 | 233518245 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FU-A5XV-01A-11D-A28B-09 | TCGA-FU-A5XV-10A-01D-A28E-09 | g.chr1:233518245C>T | c.2899C>T | c.(2899-2901)Cag>Tag | p.Q967* |
CESC | 1 | 233518365 | 233518365 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-C5-A7UH-01A-11D-A351-09 | TCGA-C5-A7UH-10A-01D-A351-09 | g.chr1:233518365C>T | c.3019C>T | c.(3019-3021)Cag>Tag | p.Q1007* |
CHOL | 1 | 233464401 | 233464409 | + | In_Frame_Del | DEL | CCGAGCGCT | CCGAGCGCT | - | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr1:233464401_233464409delCCGAGCGCT | c.627_635delCCGAGCGCT | c.(625-636)aaccgagcgctg>aag | p.209_212NRAL>K |
CHOL | 1 | 233490614 | 233490614 | + | Missense_Mutation | SNP | T | T | A | TCGA-W5-AA2X-01A-11D-A417-09 | TCGA-W5-AA2X-10A-01D-A41A-09 | g.chr1:233490614T>A | c.1168T>A | c.(1168-1170)Tcg>Acg | p.S390T |
COAD | 1 | 233482225 | 233482226 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr1:233482225_233482226insA | c.843_844insA | c.(844-846)aatfs | p.N282fs |
COAD | 1 | 233482228 | 233482228 | + | Missense_Mutation | SNP | T | T | A | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr1:233482228T>A | c.846T>A | c.(844-846)aaT>aaA | p.N282K |
COAD | 1 | 233482229 | 233482229 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:233482229A>C | c.847A>C | c.(847-849)Aaa>Caa | p.K283Q |
COAD | 1 | 233482307 | 233482307 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr1:233482307G>A | c.925G>A | c.(925-927)Gcc>Acc | p.A309T |
COAD | 1 | 233482310 | 233482310 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr1:233482310T>C | c.928T>C | c.(928-930)Tgg>Cgg | p.W310R |
COAD | 1 | 233482322 | 233482322 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr1:233482322G>A | c.940G>A | c.(940-942)Gaa>Aaa | p.E314K |
COAD | 1 | 233482322 | 233482322 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr1:233482322G>A | c.940G>A | c.(940-942)Gaa>Aaa | p.E314K |
COAD | 1 | 233489657 | 233489657 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr1:233489657C>T | c.1091C>T | c.(1090-1092)cCc>cTc | p.P364L |
COAD | 1 | 233490667 | 233490667 | + | Silent | SNP | T | T | C | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr1:233490667T>C | c.1221T>C | c.(1219-1221)acT>acC | p.T407T |
COAD | 1 | 233490690 | 233490690 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:233490690A>G | c.1244A>G | c.(1243-1245)cAt>cGt | p.H415R |
COAD | 1 | 233490744 | 233490744 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:233490744G>A | c.1298G>A | c.(1297-1299)aGa>aAa | p.R433K |
COAD | 1 | 233497801 | 233497801 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:233497801G>T | c.1314G>T | c.(1312-1314)gaG>gaT | p.E438D |
COAD | 1 | 233497811 | 233497811 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr1:233497811C>T | c.1324C>T | c.(1324-1326)Cgg>Tgg | p.R442W |
COAD | 1 | 233497879 | 233497879 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr1:233497879G>T | c.1392G>T | c.(1390-1392)gaG>gaT | p.E464D |
COAD | 1 | 233507806 | 233507806 | + | Silent | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr1:233507806G>A | c.1575G>A | c.(1573-1575)gtG>gtA | p.V525V |
COAD | 1 | 233511709 | 233511709 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3688-01A-01W-0900-09 | TCGA-AA-3688-10A-01W-0900-09 | g.chr1:233511709C>T | c.1723C>T | c.(1723-1725)Cga>Tga | p.R575* |
COAD | 1 | 233514788 | 233514789 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr1:233514788_233514789delAG | c.2036_2037delAG | c.(2035-2037)cagfs | p.Q679fs |
COAD | 1 | 233514890 | 233514890 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr1:233514890delC | c.2138delC | c.(2137-2139)tccfs | p.S713fs |
COAD | 1 | 233515325 | 233515325 | + | Missense_Mutation | SNP | A | A | G | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr1:233515325A>G | c.2573A>G | c.(2572-2574)gAt>gGt | p.D858G |
COAD | 1 | 233515416 | 233515416 | + | Silent | SNP | A | A | G | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr1:233515416A>G | c.2664A>G | c.(2662-2664)tcA>tcG | p.S888S |
COAD | 1 | 233515420 | 233515420 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr1:233515420C>A | c.2668C>A | c.(2668-2670)Cac>Aac | p.H890N |
COAD | 1 | 233515421 | 233515421 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr1:233515421A>G | c.2669A>G | c.(2668-2670)cAc>cGc | p.H890R |
COAD | 1 | 233518219 | 233518219 | + | Missense_Mutation | SNP | A | A | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr1:233518219A>T | c.2873A>T | c.(2872-2874)cAg>cTg | p.Q958L |
COAD | 1 | 233518254 | 233518254 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr1:233518254C>T | c.2908C>T | c.(2908-2910)Cag>Tag | p.Q970* |
COADREAD | 1 | 233482225 | 233482226 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr1:233482225_233482226insA | c.843_844insA | c.(844-846)aatfs | p.N282fs |
COADREAD | 1 | 233482228 | 233482228 | + | Missense_Mutation | SNP | T | T | A | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr1:233482228T>A | c.846T>A | c.(844-846)aaT>aaA | p.N282K |
COADREAD | 1 | 233482229 | 233482229 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:233482229A>C | c.847A>C | c.(847-849)Aaa>Caa | p.K283Q |
COADREAD | 1 | 233482260 | 233482260 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3582-01A-01W-0831-10 | TCGA-AG-3582-10A-01W-0831-10 | g.chr1:233482260C>T | c.878C>T | c.(877-879)gCg>gTg | p.A293V |
COADREAD | 1 | 233482307 | 233482307 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr1:233482307G>A | c.925G>A | c.(925-927)Gcc>Acc | p.A309T |
COADREAD | 1 | 233482308 | 233482308 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3898-01A-01W-1073-09 | TCGA-AG-3898-10A-01W-1073-09 | g.chr1:233482308C>T | c.926C>T | c.(925-927)gCc>gTc | p.A309V |
COADREAD | 1 | 233482310 | 233482310 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr1:233482310T>C | c.928T>C | c.(928-930)Tgg>Cgg | p.W310R |
COADREAD | 1 | 233482322 | 233482322 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr1:233482322G>A | c.940G>A | c.(940-942)Gaa>Aaa | p.E314K |
COADREAD | 1 | 233482322 | 233482322 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr1:233482322G>A | c.940G>A | c.(940-942)Gaa>Aaa | p.E314K |
COADREAD | 1 | 233489620 | 233489620 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr1:233489620G>A | c.1054G>A | c.(1054-1056)Gtg>Atg | p.V352M |
COADREAD | 1 | 233489656 | 233489656 | + | Missense_Mutation | SNP | C | C | G | TCGA-AG-3598-01A-01W-0833-10 | TCGA-AG-3598-10A-01W-0833-10 | g.chr1:233489656C>G | c.1090C>G | c.(1090-1092)Ccc>Gcc | p.P364A |
COADREAD | 1 | 233489657 | 233489657 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr1:233489657C>T | c.1091C>T | c.(1090-1092)cCc>cTc | p.P364L |
COADREAD | 1 | 233490632 | 233490632 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:233490632G>A | c.1186G>A | c.(1186-1188)Gaa>Aaa | p.E396K |
COADREAD | 1 | 233490667 | 233490667 | + | Silent | SNP | T | T | C | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr1:233490667T>C | c.1221T>C | c.(1219-1221)acT>acC | p.T407T |
COADREAD | 1 | 233490690 | 233490690 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:233490690A>G | c.1244A>G | c.(1243-1245)cAt>cGt | p.H415R |
COADREAD | 1 | 233490744 | 233490744 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:233490744G>A | c.1298G>A | c.(1297-1299)aGa>aAa | p.R433K |
COADREAD | 1 | 233497801 | 233497801 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:233497801G>T | c.1314G>T | c.(1312-1314)gaG>gaT | p.E438D |
COADREAD | 1 | 233497811 | 233497811 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr1:233497811C>T | c.1324C>T | c.(1324-1326)Cgg>Tgg | p.R442W |
COADREAD | 1 | 233497879 | 233497879 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr1:233497879G>T | c.1392G>T | c.(1390-1392)gaG>gaT | p.E464D |
COADREAD | 1 | 233497907 | 233497907 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3727-01A-01W-0899-10 | TCGA-AG-3727-10A-01W-0901-10 | g.chr1:233497907G>A | c.1420G>A | c.(1420-1422)Gtg>Atg | p.V474M |
COADREAD | 1 | 233497907 | 233497907 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr1:233497907G>A | c.1420G>A | c.(1420-1422)Gtg>Atg | p.V474M |
COADREAD | 1 | 233497916 | 233497916 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3602-01A-02W-0833-10 | TCGA-AG-3602-10A-01W-0833-10 | g.chr1:233497916C>T | c.1429C>T | c.(1429-1431)Cgg>Tgg | p.R477W |
COADREAD | 1 | 233497916 | 233497916 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A008-01A-01W-A005-10 | TCGA-AG-A008-10A-01W-A005-10 | g.chr1:233497916C>T | c.1429C>T | c.(1429-1431)Cgg>Tgg | p.R477W |
COADREAD | 1 | 233507792 | 233507792 | + | Missense_Mutation | SNP | C | C | G | TCGA-EI-6508-01A-11D-1733-10 | TCGA-EI-6508-10A-01D-1733-10 | g.chr1:233507792C>G | c.1561C>G | c.(1561-1563)Cac>Gac | p.H521D |
COADREAD | 1 | 233507806 | 233507806 | + | Silent | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr1:233507806G>A | c.1575G>A | c.(1573-1575)gtG>gtA | p.V525V |
COADREAD | 1 | 233511709 | 233511709 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3688-01A-01W-0900-09 | TCGA-AA-3688-10A-01W-0900-09 | g.chr1:233511709C>T | c.1723C>T | c.(1723-1725)Cga>Tga | p.R575* |
COADREAD | 1 | 233514788 | 233514789 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr1:233514788_233514789delAG | c.2036_2037delAG | c.(2035-2037)cagfs | p.Q679fs |
COADREAD | 1 | 233514890 | 233514890 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr1:233514890delC | c.2138delC | c.(2137-2139)tccfs | p.S713fs |
COADREAD | 1 | 233514916 | 233514916 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:233514916G>T | c.2164G>T | c.(2164-2166)Gct>Tct | p.A722S |
COADREAD | 1 | 233515325 | 233515325 | + | Missense_Mutation | SNP | A | A | G | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr1:233515325A>G | c.2573A>G | c.(2572-2574)gAt>gGt | p.D858G |
COADREAD | 1 | 233515416 | 233515416 | + | Silent | SNP | A | A | G | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr1:233515416A>G | c.2664A>G | c.(2662-2664)tcA>tcG | p.S888S |
COADREAD | 1 | 233515420 | 233515420 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr1:233515420C>A | c.2668C>A | c.(2668-2670)Cac>Aac | p.H890N |
COADREAD | 1 | 233515421 | 233515421 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr1:233515421A>G | c.2669A>G | c.(2668-2670)cAc>cGc | p.H890R |
COADREAD | 1 | 233518135 | 233518135 | + | Missense_Mutation | SNP | A | A | T | TCGA-AF-2691-01A-01W-0831-10 | TCGA-AF-2691-10A-01W-0831-10 | g.chr1:233518135A>T | c.2789A>T | c.(2788-2790)gAg>gTg | p.E930V |
COADREAD | 1 | 233518219 | 233518219 | + | Missense_Mutation | SNP | A | A | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr1:233518219A>T | c.2873A>T | c.(2872-2874)cAg>cTg | p.Q958L |
COADREAD | 1 | 233518254 | 233518254 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr1:233518254C>T | c.2908C>T | c.(2908-2910)Cag>Tag | p.Q970* |
DLBC | 1 | 233489682 | 233489682 | + | Silent | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr1:233489682G>A | c.1116G>A | c.(1114-1116)ccG>ccA | p.P372P |
DLBC | 1 | 233511675 | 233511675 | + | Missense_Mutation | SNP | A | A | C | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr1:233511675A>C | c.1689A>C | c.(1687-1689)gaA>gaC | p.E563D |
ESCA | 1 | 233511698 | 233511699 | + | Frame_Shift_Del | DEL | AC | AC | - | TCGA-L5-A4OJ-01A-11D-A27G-09 | TCGA-L5-A4OJ-11A-12D-A27G-09 | g.chr1:233511698_233511699delAC | c.1712_1713delAC | c.(1711-1713)aacfs | p.N571fs |
ESCA | 1 | 233512219 | 233512219 | + | Missense_Mutation | SNP | T | T | A | TCGA-L5-A4OW-01A-11D-A28B-09 | TCGA-L5-A4OW-11A-11D-A28E-09 | g.chr1:233512219T>A | c.1870T>A | c.(1870-1872)Tta>Ata | p.L624I |
GBM | 1 | 233511808 | 233511808 | + | Missense_Mutation | SNP | G | G | C | TCGA-14-1395-01B-11D-1845-08 | TCGA-14-1395-10A-01D-1845-08 | g.chr1:233511808G>C | c.1822G>C | c.(1822-1824)Gaa>Caa | p.E608Q |
GBM | 1 | 233515030 | 233515030 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-27-1835-01A-01D-1494-08 | TCGA-27-1835-10A-01D-1494-08 | g.chr1:233515030C>T | c.2278C>T | c.(2278-2280)Cga>Tga | p.R760* |
GBM | 1 | 233518426 | 233518426 | + | Missense_Mutation | SNP | T | T | C | TCGA-28-5218-01A-01D-1486-08 | TCGA-28-5218-10A-01D-1486-08 | g.chr1:233518426T>C | c.3080T>C | c.(3079-3081)aTa>aCa | p.I1027T |
GBMLGG | 1 | 233497841 | 233497841 | + | Missense_Mutation | SNP | C | C | G | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr1:233497841C>G | c.1354C>G | c.(1354-1356)Cag>Gag | p.Q452E |
GBMLGG | 1 | 233511808 | 233511808 | + | Missense_Mutation | SNP | G | G | C | TCGA-14-1395-01B-11D-1845-08 | TCGA-14-1395-10A-01D-1845-08 | g.chr1:233511808G>C | c.1822G>C | c.(1822-1824)Gaa>Caa | p.E608Q |
GBMLGG | 1 | 233515030 | 233515030 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-27-1835-01A-01D-1494-08 | TCGA-27-1835-10A-01D-1494-08 | g.chr1:233515030C>T | c.2278C>T | c.(2278-2280)Cga>Tga | p.R760* |
GBMLGG | 1 | 233518142 | 233518142 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:233518142A>G | c.2796A>G | c.(2794-2796)tcA>tcG | p.S932S |
GBMLGG | 1 | 233518415 | 233518415 | + | Silent | SNP | C | C | T | TCGA-TQ-A7RP-01A-21D-A34A-08 | TCGA-TQ-A7RP-10A-01D-A34A-08 | g.chr1:233518415C>T | c.3069C>T | c.(3067-3069)agC>agT | p.S1023S |
GBMLGG | 1 | 233518426 | 233518426 | + | Missense_Mutation | SNP | T | T | C | TCGA-28-5218-01A-01D-1486-08 | TCGA-28-5218-10A-01D-1486-08 | g.chr1:233518426T>C | c.3080T>C | c.(3079-3081)aTa>aCa | p.I1027T |
HNSC | 1 | 233482322 | 233482322 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr1:233482322G>A | c.940G>A | c.(940-942)Gaa>Aaa | p.E314K |
HNSC | 1 | 233482347 | 233482347 | + | Missense_Mutation | SNP | C | C | G | TCGA-P3-A6T5-01A-11D-A34J-08 | TCGA-P3-A6T5-10A-01D-A34M-08 | g.chr1:233482347C>G | c.965C>G | c.(964-966)tCt>tGt | p.S322C |
HNSC | 1 | 233489592 | 233489592 | + | Silent | SNP | C | C | T | TCGA-CV-7252-01A-11D-2012-08 | TCGA-CV-7252-10A-01D-2013-08 | g.chr1:233489592C>T | c.1026C>T | c.(1024-1026)gtC>gtT | p.V342V |
HNSC | 1 | 233514966 | 233514966 | + | Silent | SNP | C | C | T | TCGA-QK-A8Z9-01B-11D-A391-08 | TCGA-QK-A8Z9-10A-01D-A394-08 | g.chr1:233514966C>T | c.2214C>T | c.(2212-2214)gaC>gaT | p.D738D |
HNSC | 1 | 233515058 | 233515058 | + | Missense_Mutation | SNP | A | A | G | TCGA-CN-A497-01A-11D-A24D-08 | TCGA-CN-A497-10A-01D-A24F-08 | g.chr1:233515058A>G | c.2306A>G | c.(2305-2307)aAg>aGg | p.K769R |
KIPAN | 1 | 233518317 | 233518317 | + | Missense_Mutation | SNP | A | A | G | TCGA-BQ-5890-01A-11D-1589-08 | TCGA-BQ-5890-11A-01D-1589-08 | g.chr1:233518317A>G | c.2971A>G | c.(2971-2973)Aga>Gga | p.R991G |
KIPAN | 1 | 233518353 | 233518353 | + | Missense_Mutation | SNP | G | G | T | TCGA-2Z-A9JP-01A-11D-A42J-10 | TCGA-2Z-A9JP-10A-01D-A42M-10 | g.chr1:233518353G>T | c.3007G>T | c.(3007-3009)Gac>Tac | p.D1003Y |
KIRP | 1 | 233518317 | 233518317 | + | Missense_Mutation | SNP | A | A | G | TCGA-BQ-5890-01A-11D-1589-08 | TCGA-BQ-5890-11A-01D-1589-08 | g.chr1:233518317A>G | c.2971A>G | c.(2971-2973)Aga>Gga | p.R991G |
KIRP | 1 | 233518353 | 233518353 | + | Missense_Mutation | SNP | G | G | T | TCGA-2Z-A9JP-01A-11D-A42J-10 | TCGA-2Z-A9JP-10A-01D-A42M-10 | g.chr1:233518353G>T | c.3007G>T | c.(3007-3009)Gac>Tac | p.D1003Y |
LGG | 1 | 233497841 | 233497841 | + | Missense_Mutation | SNP | C | C | G | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr1:233497841C>G | c.1354C>G | c.(1354-1356)Cag>Gag | p.Q452E |
LGG | 1 | 233518142 | 233518142 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:233518142A>G | c.2796A>G | c.(2794-2796)tcA>tcG | p.S932S |
LGG | 1 | 233518415 | 233518415 | + | Silent | SNP | C | C | T | TCGA-TQ-A7RP-01A-21D-A34A-08 | TCGA-TQ-A7RP-10A-01D-A34A-08 | g.chr1:233518415C>T | c.3069C>T | c.(3067-3069)agC>agT | p.S1023S |
LIHC | 1 | 233489695 | 233489695 | + | Missense_Mutation | SNP | A | A | G | TCGA-WX-AA47-01A-11D-A38X-10 | TCGA-WX-AA47-10A-01D-A38X-10 | g.chr1:233489695A>G | c.1129A>G | c.(1129-1131)Atg>Gtg | p.M377V |
LIHC | 1 | 233514789 | 233514789 | + | Missense_Mutation | SNP | G | G | T | TCGA-XR-A8TG-01A-11D-A35Z-10 | TCGA-XR-A8TG-10A-01D-A35Z-10 | g.chr1:233514789G>T | c.2037G>T | c.(2035-2037)caG>caT | p.Q679H |
LIHC | 1 | 233518139 | 233518139 | + | Silent | SNP | C | C | T | TCGA-DD-AADE-01A-11D-A40R-10 | TCGA-DD-AADE-10A-01D-A40U-10 | g.chr1:233518139C>T | c.2793C>T | c.(2791-2793)gtC>gtT | p.V931V |
LUAD | 1 | 233464509 | 233464509 | + | Silent | SNP | G | G | C | TCGA-95-A4VK-01A-11D-A25L-08 | TCGA-95-A4VK-10A-01D-A25L-08 | g.chr1:233464509G>C | c.735G>C | c.(733-735)gcG>gcC | p.A245A |
LUAD | 1 | 233464558 | 233464558 | + | Missense_Mutation | SNP | C | C | T | TCGA-97-7938-01A-11D-2167-08 | TCGA-97-7938-10A-01D-2167-08 | g.chr1:233464558C>T | c.784C>T | c.(784-786)Cgg>Tgg | p.R262W |
LUAD | 1 | 233490644 | 233490644 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr1:233490644G>T | c.1198G>T | c.(1198-1200)Gct>Tct | p.A400S |
LUAD | 1 | 233497909 | 233497909 | + | Silent | SNP | G | G | T | TCGA-05-5425-01A-02D-1625-08 | TCGA-05-5425-10A-01D-1625-08 | g.chr1:233497909G>T | c.1422G>T | c.(1420-1422)gtG>gtT | p.V474V |
LUAD | 1 | 233507807 | 233507807 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr1:233507807C>T | c.1576C>T | c.(1576-1578)Cag>Tag | p.Q526* |
LUAD | 1 | 233507808 | 233507808 | + | Missense_Mutation | SNP | A | A | G | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr1:233507808A>G | c.1577A>G | c.(1576-1578)cAg>cGg | p.Q526R |
LUAD | 1 | 233511714 | 233511714 | + | Silent | SNP | A | A | G | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr1:233511714A>G | c.1728A>G | c.(1726-1728)caA>caG | p.Q576Q |
LUAD | 1 | 233514864 | 233514864 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4389-01A-01D-1265-08 | TCGA-05-4389-10A-01D-1265-08 | g.chr1:233514864G>T | c.2112G>T | c.(2110-2112)atG>atT | p.M704I |
LUAD | 1 | 233514942 | 233514942 | + | Silent | SNP | G | G | T | TCGA-50-5946-01A-11D-1753-08 | TCGA-50-5946-10A-01D-1753-08 | g.chr1:233514942G>T | c.2190G>T | c.(2188-2190)ctG>ctT | p.L730L |
LUAD | 1 | 233514969 | 233514969 | + | Silent | SNP | C | C | T | TCGA-55-6972-01A-11D-1945-08 | TCGA-55-6972-11A-01D-1945-08 | g.chr1:233514969C>T | c.2217C>T | c.(2215-2217)ctC>ctT | p.L739L |
LUAD | 1 | 233514980 | 233514980 | + | Missense_Mutation | SNP | A | A | T | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr1:233514980A>T | c.2228A>T | c.(2227-2229)cAt>cTt | p.H743L |
LUAD | 1 | 233518100 | 233518100 | + | Silent | SNP | C | C | T | TCGA-49-4514-01A-21D-1855-08 | TCGA-49-4514-11A-01D-1855-08 | g.chr1:233518100C>T | c.2754C>T | c.(2752-2754)tgC>tgT | p.C918C |
LUAD | 1 | 233518218 | 233518218 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr1:233518218C>T | c.2872C>T | c.(2872-2874)Cag>Tag | p.Q958* |
LUSC | 1 | 233482294 | 233482294 | + | Silent | SNP | A | A | T | TCGA-22-1012-01A-01D-1521-08 | TCGA-22-1012-11A-01D-1521-08 | g.chr1:233482294A>T | c.912A>T | c.(910-912)acA>acT | p.T304T |
LUSC | 1 | 233497839 | 233497839 | + | Missense_Mutation | SNP | T | T | G | TCGA-46-3765-01A-01D-0983-08 | TCGA-46-3765-10A-01D-0983-08 | g.chr1:233497839T>G | c.1352T>G | c.(1351-1353)cTg>cGg | p.L451R |
LUSC | 1 | 233497881 | 233497881 | + | Missense_Mutation | SNP | A | A | T | TCGA-22-4593-01A-21D-1817-08 | TCGA-22-4593-11A-01D-1817-08 | g.chr1:233497881A>T | c.1394A>T | c.(1393-1395)cAg>cTg | p.Q465L |
LUSC | 1 | 233507832 | 233507832 | + | Missense_Mutation | SNP | G | G | A | TCGA-46-6026-01A-11D-1817-08 | TCGA-46-6026-10A-01D-1817-08 | g.chr1:233507832G>A | c.1601G>A | c.(1600-1602)cGg>cAg | p.R534Q |
LUSC | 1 | 233507859 | 233507859 | + | Missense_Mutation | SNP | G | G | T | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr1:233507859G>T | c.1628G>T | c.(1627-1629)aGt>aTt | p.S543I |
LUSC | 1 | 233515049 | 233515049 | + | Missense_Mutation | SNP | G | G | T | TCGA-18-5592-01A-01D-1632-08 | TCGA-18-5592-11A-11D-1632-08 | g.chr1:233515049G>T | c.2297G>T | c.(2296-2298)cGg>cTg | p.R766L |
PAAD | 1 | 233482283 | 233482283 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-FB-AAQ6-01A-11D-A40W-08 | TCGA-FB-AAQ6-11A-11D-A40W-08 | g.chr1:233482283delA | c.901delA | c.(901-903)aaafs | p.K301fs |
PAAD | 1 | 233482285 | 233482285 | + | Missense_Mutation | SNP | A | A | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:233482285A>C | c.903A>C | c.(901-903)aaA>aaC | p.K301N |
PAAD | 1 | 233489598 | 233489598 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:233489598T>A | c.1032T>A | c.(1030-1032)taT>taA | p.Y344* |
PAAD | 1 | 233489603 | 233489603 | + | Missense_Mutation | SNP | G | G | A | TCGA-HV-A7OP-01A-11D-A33T-08 | TCGA-HV-A7OP-10A-01D-A33W-08 | g.chr1:233489603G>A | c.1037G>A | c.(1036-1038)gGc>gAc | p.G346D |
PAAD | 1 | 233497954 | 233497954 | + | Missense_Mutation | SNP | G | G | T | TCGA-FB-AAPQ-01A-11D-A40W-08 | TCGA-FB-AAPQ-11A-11D-A40W-08 | g.chr1:233497954G>T | c.1467G>T | c.(1465-1467)gaG>gaT | p.E489D |
PAAD | 1 | 233507804 | 233507804 | + | Missense_Mutation | SNP | G | G | A | TCGA-2L-AAQJ-01A-12D-A397-08 | TCGA-2L-AAQJ-11A-11D-A39A-08 | g.chr1:233507804G>A | c.1573G>A | c.(1573-1575)Gtg>Atg | p.V525M |
PAAD | 1 | 233507831 | 233507831 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:233507831C>T | c.1600C>T | c.(1600-1602)Cgg>Tgg | p.R534W |
PAAD | 1 | 233511709 | 233511709 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-2J-AAB8-01A-12D-A40W-08 | TCGA-2J-AAB8-10A-01D-A40W-08 | g.chr1:233511709C>T | c.1723C>T | c.(1723-1725)Cga>Tga | p.R575* |
PAAD | 1 | 233514763 | 233514763 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:233514763G>A | c.2011G>A | c.(2011-2013)Gat>Aat | p.D671N |
PAAD | 1 | 233514924 | 233514924 | + | Nonsense_Mutation | SNP | T | T | G | TCGA-2L-AAQI-01A-12D-A397-08 | TCGA-2L-AAQI-11A-11D-A39A-08 | g.chr1:233514924T>G | c.2172T>G | c.(2170-2172)taT>taG | p.Y724* |
PAAD | 1 | 233514930 | 233514930 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:233514930C>T | c.2178C>T | c.(2176-2178)tgC>tgT | p.C726C |
PAAD | 1 | 233515284 | 233515284 | + | Silent | SNP | A | A | G | TCGA-3A-A9I5-01A-11D-A38G-08 | TCGA-3A-A9I5-10A-01D-A38J-08 | g.chr1:233515284A>G | c.2532A>G | c.(2530-2532)ggA>ggG | p.G844G |
PRAD | 1 | 233482217 | 233482219 | + | In_Frame_Del | DEL | GAC | GAC | - | TCGA-V1-A9OF-01A-11D-A41K-08 | TCGA-V1-A9OF-10A-01D-A41N-08 | g.chr1:233482217_233482219delGAC | c.835_837delGAC | c.(835-837)gacdel | p.D279del |
PRAD | 1 | 233482357 | 233482357 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr1:233482357C>T | c.975C>T | c.(973-975)agC>agT | p.S325S |
PRAD | 1 | 233518097 | 233518097 | + | Silent | SNP | C | C | G | TCGA-HC-7230-01A-11D-2114-08 | TCGA-HC-7230-10A-01D-2115-08 | g.chr1:233518097C>G | c.2751C>G | c.(2749-2751)ctC>ctG | p.L917L |
READ | 1 | 233482260 | 233482260 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3582-01A-01W-0831-10 | TCGA-AG-3582-10A-01W-0831-10 | g.chr1:233482260C>T | c.878C>T | c.(877-879)gCg>gTg | p.A293V |
READ | 1 | 233482308 | 233482308 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3898-01A-01W-1073-09 | TCGA-AG-3898-10A-01W-1073-09 | g.chr1:233482308C>T | c.926C>T | c.(925-927)gCc>gTc | p.A309V |
READ | 1 | 233489620 | 233489620 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr1:233489620G>A | c.1054G>A | c.(1054-1056)Gtg>Atg | p.V352M |
READ | 1 | 233489656 | 233489656 | + | Missense_Mutation | SNP | C | C | G | TCGA-AG-3598-01A-01W-0833-10 | TCGA-AG-3598-10A-01W-0833-10 | g.chr1:233489656C>G | c.1090C>G | c.(1090-1092)Ccc>Gcc | p.P364A |
READ | 1 | 233490632 | 233490632 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:233490632G>A | c.1186G>A | c.(1186-1188)Gaa>Aaa | p.E396K |
READ | 1 | 233497907 | 233497907 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3727-01A-01W-0899-10 | TCGA-AG-3727-10A-01W-0901-10 | g.chr1:233497907G>A | c.1420G>A | c.(1420-1422)Gtg>Atg | p.V474M |
READ | 1 | 233497907 | 233497907 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr1:233497907G>A | c.1420G>A | c.(1420-1422)Gtg>Atg | p.V474M |
READ | 1 | 233497916 | 233497916 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3602-01A-02W-0833-10 | TCGA-AG-3602-10A-01W-0833-10 | g.chr1:233497916C>T | c.1429C>T | c.(1429-1431)Cgg>Tgg | p.R477W |
READ | 1 | 233497916 | 233497916 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A008-01A-01W-A005-10 | TCGA-AG-A008-10A-01W-A005-10 | g.chr1:233497916C>T | c.1429C>T | c.(1429-1431)Cgg>Tgg | p.R477W |
READ | 1 | 233507792 | 233507792 | + | Missense_Mutation | SNP | C | C | G | TCGA-EI-6508-01A-11D-1733-10 | TCGA-EI-6508-10A-01D-1733-10 | g.chr1:233507792C>G | c.1561C>G | c.(1561-1563)Cac>Gac | p.H521D |
READ | 1 | 233514916 | 233514916 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:233514916G>T | c.2164G>T | c.(2164-2166)Gct>Tct | p.A722S |
READ | 1 | 233518135 | 233518135 | + | Missense_Mutation | SNP | A | A | T | TCGA-AF-2691-01A-01W-0831-10 | TCGA-AF-2691-10A-01W-0831-10 | g.chr1:233518135A>T | c.2789A>T | c.(2788-2790)gAg>gTg | p.E930V |
SARC | 1 | 233482270 | 233482270 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DX-A6B8-01A-11D-A307-09 | TCGA-DX-A6B8-10A-01D-A307-09 | g.chr1:233482270G>A | c.888G>A | c.(886-888)tgG>tgA | p.W296* |
SARC | 1 | 233518139 | 233518139 | + | Silent | SNP | C | C | T | TCGA-DX-A3UC-01A-11D-A307-09 | TCGA-DX-A3UC-10A-01D-A307-09 | g.chr1:233518139C>T | c.2793C>T | c.(2791-2793)gtC>gtT | p.V931V |
SKCM | 1 | 233482258 | 233482258 | + | Silent | SNP | G | G | A | TCGA-FS-A4FC-06A-11D-A24R-08 | TCGA-FS-A4FC-10A-01D-A24R-08 | g.chr1:233482258G>A | c.876G>A | c.(874-876)ttG>ttA | p.L292L |
SKCM | 1 | 233482261 | 233482261 | + | Silent | SNP | G | G | A | TCGA-EE-A3AC-06A-11D-A196-08 | TCGA-EE-A3AC-10A-01D-A198-08 | g.chr1:233482261G>A | c.879G>A | c.(877-879)gcG>gcA | p.A293A |
SKCM | 1 | 233482338 | 233482338 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr1:233482338C>T | c.956C>T | c.(955-957)tCc>tTc | p.S319F |
SKCM | 1 | 233489572 | 233489572 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr1:233489572G>A | c.1006G>A | c.(1006-1008)Gaa>Aaa | p.E336K |
SKCM | 1 | 233489572 | 233489572 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr1:233489572G>A | c.1006G>A | c.(1006-1008)Gaa>Aaa | p.E336K |
SKCM | 1 | 233489594 | 233489594 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr1:233489594C>T | c.1028C>T | c.(1027-1029)cCc>cTc | p.P343L |
SKCM | 1 | 233489630 | 233489630 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A198-06A-11D-A196-08 | TCGA-ER-A198-10A-01D-A198-08 | g.chr1:233489630G>A | c.1064G>A | c.(1063-1065)gGg>gAg | p.G355E |
SKCM | 1 | 233489632 | 233489632 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr1:233489632G>A | c.1066G>A | c.(1066-1068)Gta>Ata | p.V356I |
SKCM | 1 | 233489663 | 233489663 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr1:233489663C>T | c.1097C>T | c.(1096-1098)cCa>cTa | p.P366L |
SKCM | 1 | 233490615 | 233490615 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GU-06A-11D-A27K-08 | TCGA-D3-A5GU-10A-01D-A27N-08 | g.chr1:233490615C>T | c.1169C>T | c.(1168-1170)tCg>tTg | p.S390L |
SKCM | 1 | 233490631 | 233490631 | + | Silent | SNP | C | C | T | TCGA-OD-A75X-06A-12D-A32N-08 | TCGA-OD-A75X-10A-01D-A32N-08 | g.chr1:233490631C>T | c.1185C>T | c.(1183-1185)ctC>ctT | p.L395L |
SKCM | 1 | 233490664 | 233490664 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GB-06A-11D-A197-08 | TCGA-EE-A2GB-10A-01D-A199-08 | g.chr1:233490664G>A | c.1218G>A | c.(1216-1218)atG>atA | p.M406I |
SKCM | 1 | 233507856 | 233507856 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A267-06A-21D-A196-08 | TCGA-GN-A267-10A-01D-A198-08 | g.chr1:233507856C>T | c.1625C>T | c.(1624-1626)tCc>tTc | p.S542F |
SKCM | 1 | 233507873 | 233507873 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr1:233507873C>T | c.1642C>T | c.(1642-1644)Ccc>Tcc | p.P548S |
SKCM | 1 | 233507881 | 233507881 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr1:233507881G>A | c.1650G>A | c.(1648-1650)atG>atA | p.M550I |
SKCM | 1 | 233511738 | 233511738 | + | Silent | SNP | G | G | A | TCGA-EE-A2GB-06A-11D-A197-08 | TCGA-EE-A2GB-10A-01D-A199-08 | g.chr1:233511738G>A | c.1752G>A | c.(1750-1752)agG>agA | p.R584R |
SKCM | 1 | 233511738 | 233511738 | + | Silent | SNP | G | G | A | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr1:233511738G>A | c.1752G>A | c.(1750-1752)agG>agA | p.R584R |
SKCM | 1 | 233511738 | 233511738 | + | Silent | SNP | G | G | A | TCGA-EE-A2GU-06A-11D-A196-08 | TCGA-EE-A2GU-10A-01D-A198-08 | g.chr1:233511738G>A | c.1752G>A | c.(1750-1752)agG>agA | p.R584R |
SKCM | 1 | 233511808 | 233511808 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2ML-06A-11D-A197-08 | TCGA-EE-A2ML-10A-01D-A199-08 | g.chr1:233511808G>A | c.1822G>A | c.(1822-1824)Gaa>Aaa | p.E608K |
SKCM | 1 | 233512192 | 233512192 | + | Missense_Mutation | SNP | G | G | A | TCGA-RP-A694-06A-11D-A30X-08 | TCGA-RP-A694-10A-01D-A30X-08 | g.chr1:233512192G>A | c.1843G>A | c.(1843-1845)Gat>Aat | p.D615N |
SKCM | 1 | 233512202 | 233512202 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr1:233512202G>A | c.1853G>A | c.(1852-1854)aGt>aAt | p.S618N |
SKCM | 1 | 233512231 | 233512231 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr1:233512231C>T | c.1882C>T | c.(1882-1884)Cag>Tag | p.Q628* |
SKCM | 1 | 233512253 | 233512253 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr1:233512253C>T | c.1904C>T | c.(1903-1905)tCa>tTa | p.S635L |
SKCM | 1 | 233514709 | 233514709 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A1Q8-06A-11D-A19A-08 | TCGA-D3-A1Q8-10A-01D-A19A-08 | g.chr1:233514709G>A | c.1957G>A | c.(1957-1959)Gga>Aga | p.G653R |
SKCM | 1 | 233514709 | 233514709 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr1:233514709G>A | c.1957G>A | c.(1957-1959)Gga>Aga | p.G653R |
SKCM | 1 | 233514713 | 233514713 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr1:233514713T>A | c.1961T>A | c.(1960-1962)tTa>tAa | p.L654* |
SKCM | 1 | 233514787 | 233514787 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr1:233514787C>T | c.2035C>T | c.(2035-2037)Cag>Tag | p.Q679* |
SKCM | 1 | 233514855 | 233514855 | + | Silent | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr1:233514855C>T | c.2103C>T | c.(2101-2103)tcC>tcT | p.S701S |
SKCM | 1 | 233514855 | 233514855 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr1:233514855C>T | c.2103C>T | c.(2101-2103)tcC>tcT | p.S701S |
SKCM | 1 | 233514909 | 233514909 | + | Silent | SNP | G | G | A | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr1:233514909G>A | c.2157G>A | c.(2155-2157)acG>acA | p.T719T |
SKCM | 1 | 233514917 | 233514917 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr1:233514917C>T | c.2165C>T | c.(2164-2166)gCt>gTt | p.A722V |
SKCM | 1 | 233514925 | 233514925 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GM-06B-11D-A196-08 | TCGA-EE-A2GM-10A-01D-A198-08 | g.chr1:233514925G>A | c.2173G>A | c.(2173-2175)Ggg>Agg | p.G725R |
SKCM | 1 | 233514925 | 233514925 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MM-06A-11D-A196-08 | TCGA-EE-A2MM-10A-01D-A198-08 | g.chr1:233514925G>A | c.2173G>A | c.(2173-2175)Ggg>Agg | p.G725R |
SKCM | 1 | 233514953 | 233514953 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr1:233514953C>T | c.2201C>T | c.(2200-2202)gCt>gTt | p.A734V |
SKCM | 1 | 233514958 | 233514958 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr1:233514958G>A | c.2206G>A | c.(2206-2208)Gga>Aga | p.G736R |
SKCM | 1 | 233515037 | 233515037 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr1:233515037G>A | c.2285G>A | c.(2284-2286)gGa>gAa | p.G762E |
SKCM | 1 | 233515097 | 233515097 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GU-06A-11D-A196-08 | TCGA-EE-A2GU-10A-01D-A198-08 | g.chr1:233515097C>T | c.2345C>T | c.(2344-2346)tCc>tTc | p.S782F |
SKCM | 1 | 233515107 | 233515107 | + | Silent | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr1:233515107G>A | c.2355G>A | c.(2353-2355)ggG>ggA | p.G785G |
SKCM | 1 | 233515108 | 233515108 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr1:233515108G>A | c.2356G>A | c.(2356-2358)Gag>Aag | p.E786K |
SKCM | 1 | 233515109 | 233515109 | + | Missense_Mutation | SNP | A | A | T | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr1:233515109A>T | c.2357A>T | c.(2356-2358)gAg>gTg | p.E786V |
SKCM | 1 | 233515161 | 233515161 | + | Silent | SNP | C | C | T | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr1:233515161C>T | c.2409C>T | c.(2407-2409)tcC>tcT | p.S803S |
SKCM | 1 | 233515261 | 233515261 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29Q-06A-11D-A197-08 | TCGA-EE-A29Q-10A-01D-A199-08 | g.chr1:233515261G>A | c.2509G>A | c.(2509-2511)Gat>Aat | p.D837N |
SKCM | 1 | 233515271 | 233515271 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr1:233515271C>T | c.2519C>T | c.(2518-2520)cCc>cTc | p.P840L |
SKCM | 1 | 233515348 | 233515348 | + | Missense_Mutation | SNP | C | C | A | TCGA-EE-A2GM-06B-11D-A196-08 | TCGA-EE-A2GM-10A-01D-A198-08 | g.chr1:233515348C>A | c.2596C>A | c.(2596-2598)Ccg>Acg | p.P866T |
SKCM | 1 | 233515349 | 233515349 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GM-06B-11D-A196-08 | TCGA-EE-A2GM-10A-01D-A198-08 | g.chr1:233515349C>T | c.2597C>T | c.(2596-2598)cCg>cTg | p.P866L |
SKCM | 1 | 233515355 | 233515355 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr1:233515355C>T | c.2603C>T | c.(2602-2604)tCc>tTc | p.S868F |
SKCM | 1 | 233518133 | 233518133 | + | Silent | SNP | G | G | A | TCGA-DA-A1I0-06A-11D-A20D-08 | TCGA-DA-A1I0-10B-01D-A20D-08 | g.chr1:233518133G>A | c.2787G>A | c.(2785-2787)agG>agA | p.R929R |
SKCM | 1 | 233518169 | 233518169 | + | Silent | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr1:233518169C>T | c.2823C>T | c.(2821-2823)atC>atT | p.I941I |
SKCM | 1 | 233518193 | 233518193 | + | Silent | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr1:233518193C>T | c.2847C>T | c.(2845-2847)tcC>tcT | p.S949S |
SKCM | 1 | 233518316 | 233518316 | + | Silent | SNP | G | G | A | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr1:233518316G>A | c.2970G>A | c.(2968-2970)gaG>gaA | p.E990E |
SKCM | 1 | 233518327 | 233518327 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr1:233518327C>T | c.2981C>T | c.(2980-2982)tCc>tTc | p.S994F |
SKCM | 1 | 233518359 | 233518359 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr1:233518359G>A | c.3013G>A | c.(3013-3015)Gaa>Aaa | p.E1005K |
SKCM | 1 | 233518443 | 233518443 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr1:233518443G>A | c.3097G>A | c.(3097-3099)Gaa>Aaa | p.E1033K |