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 | 9 | 133760173 | 133760173 | + | Silent | SNP | C | C | T | TCGA-OR-A5L2-01A-11D-A30A-10 | TCGA-OR-A5L2-10A-01D-A30A-10 | g.chr9:133760173C>T | c.2496C>T | c.(2494-2496)caC>caT | p.H832H |
BLCA | 9 | 133729477 | 133729477 | + | Missense_Mutation | SNP | G | G | A | TCGA-4Z-AA81-01A-11D-A391-08 | TCGA-4Z-AA81-10A-01D-A394-08 | g.chr9:133729477G>A | c.106G>A | c.(106-108)Gac>Aac | p.D36N |
BLCA | 9 | 133729585 | 133729585 | + | Missense_Mutation | SNP | T | T | G | TCGA-GD-A3OS-01A-12D-A21Z-08 | TCGA-GD-A3OS-10A-01D-A21Z-08 | g.chr9:133729585T>G | c.214T>G | c.(214-216)Ttt>Gtt | p.F72V |
BLCA | 9 | 133738201 | 133738201 | + | Missense_Mutation | SNP | C | C | T | TCGA-GC-A3RC-01A-11D-A22Z-08 | TCGA-GC-A3RC-10B-01D-A22Z-08 | g.chr9:133738201C>T | c.601C>T | c.(601-603)Cat>Tat | p.H201Y |
BLCA | 9 | 133738336 | 133738336 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A2LA-01A-11D-A18F-08 | TCGA-BT-A2LA-11A-11D-A18F-08 | g.chr9:133738336C>T | c.736C>T | c.(736-738)Cac>Tac | p.H246Y |
BLCA | 9 | 133750279 | 133750279 | + | Silent | SNP | G | G | A | TCGA-XF-A9T8-01A-11D-A391-08 | TCGA-XF-A9T8-10A-01D-A394-08 | g.chr9:133750279G>A | c.1110G>A | c.(1108-1110)ctG>ctA | p.L370L |
BLCA | 9 | 133750303 | 133750303 | + | Silent | SNP | G | G | A | TCGA-ZF-AA58-01A-12D-A42E-08 | TCGA-ZF-AA58-10A-01D-A42H-08 | g.chr9:133750303G>A | c.1134G>A | c.(1132-1134)aaG>aaA | p.K378K |
BLCA | 9 | 133759490 | 133759492 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-ZF-AA5N-01A-11D-A42E-08 | TCGA-ZF-AA5N-10A-01D-A42H-08 | g.chr9:133759490_133759492delAAG | c.1813_1815delAAG | c.(1813-1815)aagdel | p.K609del |
BLCA | 9 | 133759560 | 133759560 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9T6-01A-11D-A42E-08 | TCGA-XF-A9T6-10A-01D-A42H-08 | g.chr9:133759560C>G | c.1883C>G | c.(1882-1884)cCg>cGg | p.P628R |
BLCA | 9 | 133759600 | 133759600 | + | Silent | SNP | C | C | T | TCGA-CF-A47X-01A-31D-A23U-08 | TCGA-CF-A47X-10A-01D-A23U-08 | g.chr9:133759600C>T | c.1923C>T | c.(1921-1923)atC>atT | p.I641I |
BLCA | 9 | 133759700 | 133759700 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SN-01A-12D-A22Z-08 | TCGA-FD-A3SN-10A-01D-A22Z-08 | g.chr9:133759700G>A | c.2023G>A | c.(2023-2025)Gag>Aag | p.E675K |
BLCA | 9 | 133759972 | 133759972 | + | Silent | SNP | G | G | A | TCGA-GD-A3OP-01A-21D-A21Z-08 | TCGA-GD-A3OP-10A-01D-A21Z-08 | g.chr9:133759972G>A | c.2295G>A | c.(2293-2295)aaG>aaA | p.K765K |
BLCA | 9 | 133760298 | 133760298 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A1A3-01A-11D-A13W-08 | TCGA-DK-A1A3-10A-01D-A13W-08 | g.chr9:133760298G>A | c.2621G>A | c.(2620-2622)aGa>aAa | p.R874K |
BLCA | 9 | 133760714 | 133760714 | + | Missense_Mutation | SNP | C | C | T | TCGA-E7-A541-01A-11D-A26M-08 | TCGA-E7-A541-10A-01D-A26K-08 | g.chr9:133760714C>T | c.3037C>T | c.(3037-3039)Cgg>Tgg | p.R1013W |
BLCA | 9 | 133760866 | 133760866 | + | Silent | SNP | C | C | G | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr9:133760866C>G | c.3189C>G | c.(3187-3189)ctC>ctG | p.L1063L |
BRCA | 9 | 133589825 | 133589825 | + | IGR | SNP | A | A | G | TCGA-AC-A3EH-01A-22D-A228-09 | TCGA-AC-A3EH-11B-21D-A22A-09 | g.chr9:133589825A>G | | | |
BRCA | 9 | 133729582 | 133729582 | + | Missense_Mutation | SNP | G | G | A | TCGA-E2-A1LB-01A-11D-A142-09 | TCGA-E2-A1LB-11A-22D-A142-09 | g.chr9:133729582G>A | c.211G>A | c.(211-213)Gat>Aat | p.D71N |
BRCA | 9 | 133750254 | 133750254 | + | Splice_Site | SNP | G | G | C | TCGA-B6-A0RV-01A-11D-A099-09 | TCGA-B6-A0RV-10A-01D-A099-09 | g.chr9:133750254G>C | | c.e7-1 | |
BRCA | 9 | 133753849 | 133753849 | + | Missense_Mutation | SNP | T | T | C | TCGA-A8-A094-01A-11W-A019-09 | TCGA-A8-A094-10A-01W-A021-09 | g.chr9:133753849T>C | c.1318T>C | c.(1318-1320)Tac>Cac | p.Y440H |
BRCA | 9 | 133753945 | 133753945 | + | Missense_Mutation | SNP | A | A | T | TCGA-E9-A54X-01A-11D-A25Q-09 | TCGA-E9-A54X-10A-01D-A25Q-09 | g.chr9:133753945A>T | c.1414A>T | c.(1414-1416)Atg>Ttg | p.M472L |
BRCA | 9 | 133755477 | 133755477 | + | Missense_Mutation | SNP | C | C | A | TCGA-BH-A0B3-01A-11W-A071-09 | TCGA-BH-A0B3-11B-21W-A100-09 | g.chr9:133755477C>A | c.1446C>A | c.(1444-1446)gaC>gaA | p.D482E |
BRCA | 9 | 133759439 | 133759439 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr9:133759439G>C | c.1762G>C | c.(1762-1764)Gag>Cag | p.E588Q |
CESC | 9 | 133729451 | 133729451 | + | Splice_Site | SNP | A | A | T | TCGA-C5-A7CM-01A-11D-A33O-09 | TCGA-C5-A7CM-10A-01D-A33O-09 | g.chr9:133729451A>T | c.80A>T | c.(79-81)gAa>gTa | p.E27V |
CESC | 9 | 133729510 | 133729510 | + | Missense_Mutation | SNP | C | C | T | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr9:133729510C>T | c.139C>T | c.(139-141)Cgt>Tgt | p.R47C |
CESC | 9 | 133730462 | 133730462 | + | Silent | SNP | C | C | T | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr9:133730462C>T | c.528C>T | c.(526-528)atC>atT | p.I176I |
CESC | 9 | 133750392 | 133750392 | + | Missense_Mutation | SNP | C | C | G | TCGA-UC-A7PF-01A-11D-A351-09 | TCGA-UC-A7PF-11A-31D-A351-09 | g.chr9:133750392C>G | c.1223C>G | c.(1222-1224)cCc>cGc | p.P408R |
CESC | 9 | 133753889 | 133753891 | + | In_Frame_Del | DEL | AGA | AGA | - | TCGA-EA-A1QT-01A-11D-A14W-08 | TCGA-EA-A1QT-10A-01D-A14W-08 | g.chr9:133753889_133753891delAGA | c.1358_1360delAGA | c.(1357-1362)gagaag>gag | p.K454del |
CESC | 9 | 133759498 | 133759498 | + | Silent | SNP | G | G | A | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr9:133759498G>A | c.1821G>A | c.(1819-1821)aaG>aaA | p.K607K |
CESC | 9 | 133759592 | 133759592 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EA-A3HR-01A-11D-A20U-09 | TCGA-EA-A3HR-10A-01D-A20U-09 | g.chr9:133759592C>T | c.1915C>T | c.(1915-1917)Cga>Tga | p.R639* |
CESC | 9 | 133759698 | 133759698 | + | Missense_Mutation | SNP | G | G | A | TCGA-HG-A2PA-01A-11D-A20U-09 | TCGA-HG-A2PA-10B-01D-A20U-09 | g.chr9:133759698G>A | c.2021G>A | c.(2020-2022)cGg>cAg | p.R674Q |
CESC | 9 | 133760373 | 133760373 | + | Missense_Mutation | SNP | C | C | T | TCGA-EA-A44S-01A-12D-A26G-09 | TCGA-EA-A44S-10A-01D-A26G-09 | g.chr9:133760373C>T | c.2696C>T | c.(2695-2697)cCg>cTg | p.P899L |
CESC | 9 | 133760730 | 133760730 | + | Missense_Mutation | SNP | C | C | A | TCGA-MU-A5YI-01A-11D-A32I-09 | TCGA-MU-A5YI-10A-01D-A32I-09 | g.chr9:133760730C>A | c.3053C>A | c.(3052-3054)cCt>cAt | p.P1018H |
COAD | 9 | 133729510 | 133729510 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr9:133729510C>T | c.139C>T | c.(139-141)Cgt>Tgt | p.R47C |
COAD | 9 | 133729511 | 133729511 | + | Missense_Mutation | SNP | G | G | T | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr9:133729511G>T | c.140G>T | c.(139-141)cGt>cTt | p.R47L |
COAD | 9 | 133729537 | 133729537 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr9:133729537G>A | c.166G>A | c.(166-168)Gct>Act | p.A56T |
COAD | 9 | 133729569 | 133729569 | + | Silent | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr9:133729569C>T | c.198C>T | c.(196-198)ttC>ttT | p.F66F |
COAD | 9 | 133730388 | 133730388 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr9:133730388C>T | c.454C>T | c.(454-456)Cgt>Tgt | p.R152C |
COAD | 9 | 133730432 | 133730432 | + | Silent | SNP | A | A | G | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr9:133730432A>G | c.498A>G | c.(496-498)agA>agG | p.R166R |
COAD | 9 | 133738331 | 133738331 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6161-01A-11D-1650-10 | TCGA-CM-6161-10A-01D-1650-10 | g.chr9:133738331T>C | c.731T>C | c.(730-732)aTg>aCg | p.M244T |
COAD | 9 | 133738358 | 133738358 | + | Missense_Mutation | SNP | A | A | T | TCGA-AZ-5407-01A-01D-1719-10 | TCGA-AZ-5407-10A-01D-1719-10 | g.chr9:133738358A>T | c.758A>T | c.(757-759)tAc>tTc | p.Y253F |
COAD | 9 | 133738359 | 133738359 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-A02K-01A-21W-A096-10 | TCGA-AA-A02K-10A-01W-A096-10 | g.chr9:133738359C>A | c.759C>A | c.(757-759)taC>taA | p.Y253* |
COAD | 9 | 133738364 | 133738364 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6321-01A-11D-1719-10 | TCGA-G4-6321-10A-01D-1720-10 | g.chr9:133738364A>G | c.764A>G | c.(763-765)gAg>gGg | p.E255G |
COAD | 9 | 133747520 | 133747520 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6310-01A-11D-1719-10 | TCGA-G4-6310-10A-01D-1720-10 | g.chr9:133747520A>G | c.827A>G | c.(826-828)gAc>gGc | p.D276G |
COAD | 9 | 133747529 | 133747529 | + | Missense_Mutation | SNP | A | A | G | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr9:133747529A>G | c.836A>G | c.(835-837)gAg>gGg | p.E279G |
COAD | 9 | 133747588 | 133747588 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-7000-01A-11D-1924-10 | TCGA-D5-7000-10A-01D-1924-10 | g.chr9:133747588G>A | c.895G>A | c.(895-897)Gtg>Atg | p.V299M |
COAD | 9 | 133748289 | 133748289 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr9:133748289T>C | c.950T>C | c.(949-951)tTc>tCc | p.F317S |
COAD | 9 | 133748328 | 133748328 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr9:133748328G>A | c.989G>A | c.(988-990)tGc>tAc | p.C330Y |
COAD | 9 | 133750278 | 133750278 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr9:133750278T>C | c.1109T>C | c.(1108-1110)cTg>cCg | p.L370P |
COAD | 9 | 133750298 | 133750298 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr9:133750298G>A | c.1129G>A | c.(1129-1131)Gtg>Atg | p.V377M |
COAD | 9 | 133750319 | 133750319 | + | Silent | SNP | C | C | T | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr9:133750319C>T | c.1150C>T | c.(1150-1152)Ctg>Ttg | p.L384L |
COAD | 9 | 133750320 | 133750320 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6536-01A-11D-1719-10 | TCGA-D5-6536-10A-01D-1719-10 | g.chr9:133750320T>C | c.1151T>C | c.(1150-1152)cTg>cCg | p.L384P |
COAD | 9 | 133750321 | 133750321 | + | Silent | SNP | G | G | A | TCGA-CM-5349-01A-21D-1719-10 | TCGA-CM-5349-10A-01D-1719-10 | g.chr9:133750321G>A | c.1152G>A | c.(1150-1152)ctG>ctA | p.L384L |
COAD | 9 | 133750356 | 133750356 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr9:133750356A>G | c.1187A>G | c.(1186-1188)cAt>cGt | p.H396R |
COAD | 9 | 133750357 | 133750357 | + | Silent | SNP | T | T | C | TCGA-CM-5863-01A-21D-1835-10 | TCGA-CM-5863-10A-01D-1835-10 | g.chr9:133750357T>C | c.1188T>C | c.(1186-1188)caT>caC | p.H396H |
COAD | 9 | 133750418 | 133750418 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6901-01A-11D-1924-10 | TCGA-AD-6901-10A-01D-1924-10 | g.chr9:133750418T>C | c.1249T>C | c.(1249-1251)Tcc>Ccc | p.S417P |
COAD | 9 | 133750420 | 133750420 | + | Silent | SNP | C | C | A | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr9:133750420C>A | c.1251C>A | c.(1249-1251)tcC>tcA | p.S417S |
COAD | 9 | 133753907 | 133753907 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr9:133753907A>G | c.1376A>G | c.(1375-1377)gAg>gGg | p.E459G |
COAD | 9 | 133753907 | 133753907 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6163-01A-11D-1650-10 | TCGA-CM-6163-10A-01D-1650-10 | g.chr9:133753907A>G | c.1376A>G | c.(1375-1377)gAg>gGg | p.E459G |
COAD | 9 | 133753908 | 133753908 | + | Missense_Mutation | SNP | G | G | T | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr9:133753908G>T | c.1377G>T | c.(1375-1377)gaG>gaT | p.E459D |
COAD | 9 | 133755462 | 133755462 | + | Silent | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr9:133755462G>A | c.1431G>A | c.(1429-1431)caG>caA | p.Q477Q |
COAD | 9 | 133755915 | 133755915 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr9:133755915C>T | c.1542C>T | c.(1540-1542)ggC>ggT | p.G514G |
COAD | 9 | 133759406 | 133759406 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr9:133759406C>T | c.1729C>T | c.(1729-1731)Cga>Tga | p.R577* |
COAD | 9 | 133759524 | 133759524 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr9:133759524A>G | c.1847A>G | c.(1846-1848)aAa>aGa | p.K616R |
COAD | 9 | 133759812 | 133759812 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr9:133759812G>A | c.2135G>A | c.(2134-2136)cGc>cAc | p.R712H |
COAD | 9 | 133760374 | 133760374 | + | Silent | SNP | G | G | A | TCGA-CM-4746-01A-01D-1408-10 | TCGA-CM-4746-10A-01D-1408-10 | g.chr9:133760374G>A | c.2697G>A | c.(2695-2697)ccG>ccA | p.P899P |
COAD | 9 | 133760392 | 133760392 | + | Silent | SNP | C | C | T | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr9:133760392C>T | c.2715C>T | c.(2713-2715)gcC>gcT | p.A905A |
COAD | 9 | 133760430 | 133760430 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr9:133760430C>T | c.2753C>T | c.(2752-2754)cCg>cTg | p.P918L |
COAD | 9 | 133760628 | 133760628 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6539-01A-11D-1719-10 | TCGA-D5-6539-10A-01D-1719-10 | g.chr9:133760628C>T | c.2951C>T | c.(2950-2952)aCg>aTg | p.T984M |
COAD | 9 | 133760743 | 133760743 | + | Silent | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr9:133760743C>T | c.3066C>T | c.(3064-3066)atC>atT | p.I1022I |
COAD | 9 | 133760818 | 133760818 | + | Silent | SNP | C | C | T | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr9:133760818C>T | c.3141C>T | c.(3139-3141)tcC>tcT | p.S1047S |
COAD | 9 | 133760833 | 133760833 | + | Silent | SNP | C | C | T | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr9:133760833C>T | c.3156C>T | c.(3154-3156)agC>agT | p.S1052S |
COAD | 9 | 133760960 | 133760960 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr9:133760960C>T | c.3283C>T | c.(3283-3285)Cgg>Tgg | p.R1095W |
COADREAD | 9 | 133729510 | 133729510 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr9:133729510C>T | c.139C>T | c.(139-141)Cgt>Tgt | p.R47C |
COADREAD | 9 | 133729511 | 133729511 | + | Missense_Mutation | SNP | G | G | T | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr9:133729511G>T | c.140G>T | c.(139-141)cGt>cTt | p.R47L |
COADREAD | 9 | 133729537 | 133729537 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr9:133729537G>A | c.166G>A | c.(166-168)Gct>Act | p.A56T |
COADREAD | 9 | 133729537 | 133729537 | + | Missense_Mutation | SNP | G | G | A | TCGA-AH-6644-01A-21D-1826-10 | TCGA-AH-6644-10A-01D-1826-10 | g.chr9:133729537G>A | c.166G>A | c.(166-168)Gct>Act | p.A56T |
COADREAD | 9 | 133729569 | 133729569 | + | Silent | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr9:133729569C>T | c.198C>T | c.(196-198)ttC>ttT | p.F66F |
COADREAD | 9 | 133729569 | 133729569 | + | Silent | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:133729569C>T | c.198C>T | c.(196-198)ttC>ttT | p.F66F |
COADREAD | 9 | 133730245 | 133730245 | + | Missense_Mutation | SNP | C | C | T | TCGA-DY-A0XA-01A-11D-A152-10 | TCGA-DY-A0XA-10A-01D-A152-10 | g.chr9:133730245C>T | c.311C>T | c.(310-312)aCc>aTc | p.T104I |
COADREAD | 9 | 133730388 | 133730388 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr9:133730388C>T | c.454C>T | c.(454-456)Cgt>Tgt | p.R152C |
COADREAD | 9 | 133730432 | 133730432 | + | Silent | SNP | A | A | G | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr9:133730432A>G | c.498A>G | c.(496-498)agA>agG | p.R166R |
COADREAD | 9 | 133738331 | 133738331 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6161-01A-11D-1650-10 | TCGA-CM-6161-10A-01D-1650-10 | g.chr9:133738331T>C | c.731T>C | c.(730-732)aTg>aCg | p.M244T |
COADREAD | 9 | 133738358 | 133738358 | + | Missense_Mutation | SNP | A | A | T | TCGA-AZ-5407-01A-01D-1719-10 | TCGA-AZ-5407-10A-01D-1719-10 | g.chr9:133738358A>T | c.758A>T | c.(757-759)tAc>tTc | p.Y253F |
COADREAD | 9 | 133738359 | 133738359 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-A02K-01A-21W-A096-10 | TCGA-AA-A02K-10A-01W-A096-10 | g.chr9:133738359C>A | c.759C>A | c.(757-759)taC>taA | p.Y253* |
COADREAD | 9 | 133738364 | 133738364 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6321-01A-11D-1719-10 | TCGA-G4-6321-10A-01D-1720-10 | g.chr9:133738364A>G | c.764A>G | c.(763-765)gAg>gGg | p.E255G |
COADREAD | 9 | 133747520 | 133747520 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6310-01A-11D-1719-10 | TCGA-G4-6310-10A-01D-1720-10 | g.chr9:133747520A>G | c.827A>G | c.(826-828)gAc>gGc | p.D276G |
COADREAD | 9 | 133747529 | 133747529 | + | Missense_Mutation | SNP | A | A | G | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr9:133747529A>G | c.836A>G | c.(835-837)gAg>gGg | p.E279G |
COADREAD | 9 | 133747588 | 133747588 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-7000-01A-11D-1924-10 | TCGA-D5-7000-10A-01D-1924-10 | g.chr9:133747588G>A | c.895G>A | c.(895-897)Gtg>Atg | p.V299M |
COADREAD | 9 | 133748289 | 133748289 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr9:133748289T>C | c.950T>C | c.(949-951)tTc>tCc | p.F317S |
COADREAD | 9 | 133748328 | 133748328 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr9:133748328G>A | c.989G>A | c.(988-990)tGc>tAc | p.C330Y |
COADREAD | 9 | 133748390 | 133748390 | + | Missense_Mutation | SNP | A | A | G | TCGA-EI-6508-01A-11D-1733-10 | TCGA-EI-6508-10A-01D-1733-10 | g.chr9:133748390A>G | c.1051A>G | c.(1051-1053)Atg>Gtg | p.M351V |
COADREAD | 9 | 133750278 | 133750278 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr9:133750278T>C | c.1109T>C | c.(1108-1110)cTg>cCg | p.L370P |
COADREAD | 9 | 133750298 | 133750298 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr9:133750298G>A | c.1129G>A | c.(1129-1131)Gtg>Atg | p.V377M |
COADREAD | 9 | 133750319 | 133750319 | + | Silent | SNP | C | C | T | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr9:133750319C>T | c.1150C>T | c.(1150-1152)Ctg>Ttg | p.L384L |
COADREAD | 9 | 133750320 | 133750320 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6536-01A-11D-1719-10 | TCGA-D5-6536-10A-01D-1719-10 | g.chr9:133750320T>C | c.1151T>C | c.(1150-1152)cTg>cCg | p.L384P |
COADREAD | 9 | 133750321 | 133750321 | + | Silent | SNP | G | G | A | TCGA-CM-5349-01A-21D-1719-10 | TCGA-CM-5349-10A-01D-1719-10 | g.chr9:133750321G>A | c.1152G>A | c.(1150-1152)ctG>ctA | p.L384L |
COADREAD | 9 | 133750356 | 133750356 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr9:133750356A>G | c.1187A>G | c.(1186-1188)cAt>cGt | p.H396R |
COADREAD | 9 | 133750357 | 133750357 | + | Silent | SNP | T | T | C | TCGA-CM-5863-01A-21D-1835-10 | TCGA-CM-5863-10A-01D-1835-10 | g.chr9:133750357T>C | c.1188T>C | c.(1186-1188)caT>caC | p.H396H |
COADREAD | 9 | 133750418 | 133750418 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6901-01A-11D-1924-10 | TCGA-AD-6901-10A-01D-1924-10 | g.chr9:133750418T>C | c.1249T>C | c.(1249-1251)Tcc>Ccc | p.S417P |
COADREAD | 9 | 133750420 | 133750420 | + | Silent | SNP | C | C | A | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr9:133750420C>A | c.1251C>A | c.(1249-1251)tcC>tcA | p.S417S |
COADREAD | 9 | 133753907 | 133753907 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr9:133753907A>G | c.1376A>G | c.(1375-1377)gAg>gGg | p.E459G |
COADREAD | 9 | 133753907 | 133753907 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6163-01A-11D-1650-10 | TCGA-CM-6163-10A-01D-1650-10 | g.chr9:133753907A>G | c.1376A>G | c.(1375-1377)gAg>gGg | p.E459G |
COADREAD | 9 | 133753908 | 133753908 | + | Missense_Mutation | SNP | G | G | T | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr9:133753908G>T | c.1377G>T | c.(1375-1377)gaG>gaT | p.E459D |
COADREAD | 9 | 133755462 | 133755462 | + | Silent | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr9:133755462G>A | c.1431G>A | c.(1429-1431)caG>caA | p.Q477Q |
COADREAD | 9 | 133755915 | 133755915 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr9:133755915C>T | c.1542C>T | c.(1540-1542)ggC>ggT | p.G514G |
COADREAD | 9 | 133759406 | 133759406 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr9:133759406C>T | c.1729C>T | c.(1729-1731)Cga>Tga | p.R577* |
COADREAD | 9 | 133759524 | 133759524 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr9:133759524A>G | c.1847A>G | c.(1846-1848)aAa>aGa | p.K616R |
COADREAD | 9 | 133759812 | 133759812 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr9:133759812G>A | c.2135G>A | c.(2134-2136)cGc>cAc | p.R712H |
COADREAD | 9 | 133760130 | 133760130 | + | Missense_Mutation | SNP | T | T | C | TCGA-EF-5830-01A-01D-1657-10 | TCGA-EF-5830-10A-01D-1657-10 | g.chr9:133760130T>C | c.2453T>C | c.(2452-2454)cTc>cCc | p.L818P |
COADREAD | 9 | 133760374 | 133760374 | + | Silent | SNP | G | G | A | TCGA-CM-4746-01A-01D-1408-10 | TCGA-CM-4746-10A-01D-1408-10 | g.chr9:133760374G>A | c.2697G>A | c.(2695-2697)ccG>ccA | p.P899P |
COADREAD | 9 | 133760392 | 133760392 | + | Silent | SNP | C | C | T | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr9:133760392C>T | c.2715C>T | c.(2713-2715)gcC>gcT | p.A905A |
COADREAD | 9 | 133760430 | 133760430 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr9:133760430C>T | c.2753C>T | c.(2752-2754)cCg>cTg | p.P918L |
COADREAD | 9 | 133760628 | 133760628 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6539-01A-11D-1719-10 | TCGA-D5-6539-10A-01D-1719-10 | g.chr9:133760628C>T | c.2951C>T | c.(2950-2952)aCg>aTg | p.T984M |
COADREAD | 9 | 133760743 | 133760743 | + | Silent | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr9:133760743C>T | c.3066C>T | c.(3064-3066)atC>atT | p.I1022I |
COADREAD | 9 | 133760818 | 133760818 | + | Silent | SNP | C | C | T | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr9:133760818C>T | c.3141C>T | c.(3139-3141)tcC>tcT | p.S1047S |
COADREAD | 9 | 133760833 | 133760833 | + | Silent | SNP | C | C | T | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr9:133760833C>T | c.3156C>T | c.(3154-3156)agC>agT | p.S1052S |
COADREAD | 9 | 133760960 | 133760960 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr9:133760960C>T | c.3283C>T | c.(3283-3285)Cgg>Tgg | p.R1095W |
DLBC | 9 | 133729485 | 133729485 | + | Silent | SNP | G | G | A | TCGA-FF-A7CR-01A-11D-A382-10 | TCGA-FF-A7CR-10A-01D-A385-10 | g.chr9:133729485G>A | c.114G>A | c.(112-114)gaG>gaA | p.E38E |
DLBC | 9 | 133755528 | 133755528 | + | Silent | SNP | A | A | G | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr9:133755528A>G | c.1497A>G | c.(1495-1497)gaA>gaG | p.E499E |
DLBC | 9 | 133755528 | 133755528 | + | Silent | SNP | A | A | G | TCGA-G8-6914-01A-11D-2210-10 | TCGA-G8-6914-14A-01D-2210-10 | g.chr9:133755528A>G | c.1497A>G | c.(1495-1497)gaA>gaG | p.E499E |
DLBC | 9 | 133759546 | 133759546 | + | Silent | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr9:133759546G>A | c.1869G>A | c.(1867-1869)gaG>gaA | p.E623E |
DLBC | 9 | 133759686 | 133759686 | + | Missense_Mutation | SNP | A | A | G | TCGA-G8-6907-01A-11D-2210-10 | TCGA-G8-6907-14A-01D-2210-10 | g.chr9:133759686A>G | c.2009A>G | c.(2008-2010)aAt>aGt | p.N670S |
DLBC | 9 | 133760029 | 133760029 | + | Silent | SNP | C | C | G | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr9:133760029C>G | c.2352C>G | c.(2350-2352)ccC>ccG | p.P784P |
DLBC | 9 | 133760029 | 133760029 | + | Silent | SNP | C | C | G | TCGA-G8-6914-01A-11D-2210-10 | TCGA-G8-6914-14A-01D-2210-10 | g.chr9:133760029C>G | c.2352C>G | c.(2350-2352)ccC>ccG | p.P784P |
DLBC | 9 | 133760106 | 133760106 | + | Missense_Mutation | SNP | C | C | T | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr9:133760106C>T | c.2429C>T | c.(2428-2430)cCg>cTg | p.P810L |
DLBC | 9 | 133760380 | 133760380 | + | Silent | SNP | C | C | G | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr9:133760380C>G | c.2703C>G | c.(2701-2703)ccC>ccG | p.P901P |
DLBC | 9 | 133760592 | 133760592 | + | Missense_Mutation | SNP | C | C | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr9:133760592C>T | c.2915C>T | c.(2914-2916)tCg>tTg | p.S972L |
DLBC | 9 | 133761001 | 133761001 | + | Silent | SNP | A | A | G | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr9:133761001A>G | c.3324A>G | c.(3322-3324)ccA>ccG | p.P1108P |
DLBC | 9 | 133761001 | 133761001 | + | Silent | SNP | A | A | G | TCGA-G8-6914-01A-11D-2210-10 | TCGA-G8-6914-14A-01D-2210-10 | g.chr9:133761001A>G | c.3324A>G | c.(3322-3324)ccA>ccG | p.P1108P |
ESCA | 9 | 133738375 | 133738375 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A4OH-01A-11D-A27G-09 | TCGA-L5-A4OH-11A-11D-A27G-09 | g.chr9:133738375G>A | c.775G>A | c.(775-777)Ggc>Agc | p.G259S |
ESCA | 9 | 133750256 | 133750256 | + | Splice_Site | SNP | G | G | C | TCGA-VR-A8EX-01A-11D-A36J-09 | TCGA-VR-A8EX-10A-01D-A36M-09 | g.chr9:133750256G>C | c.1087G>C | c.(1087-1089)Gat>Cat | p.D363H |
ESCA | 9 | 133760107 | 133760107 | + | Silent | SNP | G | G | A | TCGA-JY-A6FH-01A-11D-A33E-09 | TCGA-JY-A6FH-10A-01D-A33H-09 | g.chr9:133760107G>A | c.2430G>A | c.(2428-2430)ccG>ccA | p.P810P |
GBM | 9 | 133750310 | 133750310 | + | Missense_Mutation | SNP | G | G | T | TCGA-06-5859-01A-01D-1696-08 | TCGA-06-5859-10A-01D-1696-08 | g.chr9:133750310G>T | c.1141G>T | c.(1141-1143)Gat>Tat | p.D381Y |
GBM | 9 | 133760582 | 133760582 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-5412-01A-01D-1696-08 | TCGA-06-5412-10A-01D-1696-08 | g.chr9:133760582G>A | c.2905G>A | c.(2905-2907)Gcc>Acc | p.A969T |
GBMLGG | 9 | 133729608 | 133729608 | + | Silent | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133729608T>G | c.237T>G | c.(235-237)acT>acG | p.T79T |
GBMLGG | 9 | 133750263 | 133750263 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133750263C>A | c.1094C>A | c.(1093-1095)gCt>gAt | p.A365D |
GBMLGG | 9 | 133750310 | 133750310 | + | Missense_Mutation | SNP | G | G | T | TCGA-06-5859-01A-01D-1696-08 | TCGA-06-5859-10A-01D-1696-08 | g.chr9:133750310G>T | c.1141G>T | c.(1141-1143)Gat>Tat | p.D381Y |
GBMLGG | 9 | 133753948 | 133753948 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133753948C>T | c.1417C>T | c.(1417-1419)Cga>Tga | p.R473* |
GBMLGG | 9 | 133760330 | 133760330 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133760330C>T | c.2653C>T | c.(2653-2655)Cca>Tca | p.P885S |
GBMLGG | 9 | 133760582 | 133760582 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-5412-01A-01D-1696-08 | TCGA-06-5412-10A-01D-1696-08 | g.chr9:133760582G>A | c.2905G>A | c.(2905-2907)Gcc>Acc | p.A969T |
GBMLGG | 9 | 133761036 | 133761036 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133761036C>T | c.3359C>T | c.(3358-3360)tCg>tTg | p.S1120L |
HNSC | 9 | 133729579 | 133729579 | + | Missense_Mutation | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr9:133729579T>C | c.208T>C | c.(208-210)Tat>Cat | p.Y70H |
HNSC | 9 | 133738189 | 133738189 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-CN-A6V3-01A-12D-A34J-08 | TCGA-CN-A6V3-10A-01D-A34M-08 | g.chr9:133738189G>T | c.589G>T | c.(589-591)Gag>Tag | p.E197* |
HNSC | 9 | 133738362 | 133738362 | + | Silent | SNP | G | G | A | TCGA-CV-7254-01A-11D-2012-08 | TCGA-CV-7254-10A-01D-2013-08 | g.chr9:133738362G>A | c.762G>A | c.(760-762)ggG>ggA | p.G254G |
HNSC | 9 | 133748276 | 133748276 | + | Missense_Mutation | SNP | A | A | G | TCGA-IQ-A61L-01A-11D-A30E-08 | TCGA-IQ-A61L-10A-01D-A30H-08 | g.chr9:133748276A>G | c.937A>G | c.(937-939)Atc>Gtc | p.I313V |
HNSC | 9 | 133748417 | 133748417 | + | Missense_Mutation | SNP | A | A | G | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr9:133748417A>G | c.1078A>G | c.(1078-1080)Atc>Gtc | p.I360V |
HNSC | 9 | 133750435 | 133750435 | + | Silent | SNP | C | C | A | TCGA-CV-A6JZ-01A-11D-A31L-08 | TCGA-CV-A6JZ-10A-01D-A31J-08 | g.chr9:133750435C>A | c.1266C>A | c.(1264-1266)gtC>gtA | p.V422V |
HNSC | 9 | 133755972 | 133755972 | + | Missense_Mutation | SNP | G | G | T | TCGA-BA-A6DD-01A-12D-A31L-08 | TCGA-BA-A6DD-10A-01D-A31J-08 | g.chr9:133755972G>T | c.1599G>T | c.(1597-1599)agG>agT | p.R533S |
HNSC | 9 | 133759490 | 133759492 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-CQ-5332-01A-01D-1683-08 | TCGA-CQ-5332-10A-01D-1683-08 | g.chr9:133759490_133759492delAAG | c.1813_1815delAAG | c.(1813-1815)aagdel | p.K609del |
HNSC | 9 | 133759490 | 133759492 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-MZ-A5BI-01A-31D-A34J-08 | TCGA-MZ-A5BI-10C-01D-A34M-08 | g.chr9:133759490_133759492delAAG | c.1813_1815delAAG | c.(1813-1815)aagdel | p.K609del |
HNSC | 9 | 133760374 | 133760374 | + | Silent | SNP | G | G | A | TCGA-UF-A71D-01A-12D-A34J-08 | TCGA-UF-A71D-10B-01D-A34M-08 | g.chr9:133760374G>A | c.2697G>A | c.(2695-2697)ccG>ccA | p.P899P |
HNSC | 9 | 133760623 | 133760623 | + | Silent | SNP | C | C | A | TCGA-CN-6018-01A-11D-1683-08 | TCGA-CN-6018-10A-01D-1683-08 | g.chr9:133760623C>A | c.2946C>A | c.(2944-2946)ccC>ccA | p.P982P |
HNSC | 9 | 133760654 | 133760654 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-A63U-01A-11D-A30E-08 | TCGA-CN-A63U-10A-01D-A30H-08 | g.chr9:133760654G>C | c.2977G>C | c.(2977-2979)Gca>Cca | p.A993P |
KICH | 9 | 133748274 | 133748274 | + | Missense_Mutation | SNP | A | A | G | TCGA-KM-8443-01A-11D-2310-10 | TCGA-KM-8443-10A-01D-2311-10 | g.chr9:133748274A>G | c.935A>G | c.(934-936)tAt>tGt | p.Y312C |
KIPAN | 9 | 133729596 | 133729596 | + | Missense_Mutation | SNP | T | T | G | TCGA-B0-5696-01A-11D-1534-10 | TCGA-B0-5696-11A-01D-1534-10 | g.chr9:133729596T>G | c.225T>G | c.(223-225)agT>agG | p.S75R |
KIPAN | 9 | 133730265 | 133730265 | + | Missense_Mutation | SNP | G | G | C | TCGA-EV-5903-01A-11D-1589-08 | TCGA-EV-5903-10A-01D-1589-08 | g.chr9:133730265G>C | c.331G>C | c.(331-333)Gtc>Ctc | p.V111L |
KIPAN | 9 | 133730431 | 133730431 | + | Missense_Mutation | SNP | G | G | A | TCGA-BP-4159-01A-02D-1366-10 | TCGA-BP-4159-11A-01D-1366-10 | g.chr9:133730431G>A | c.497G>A | c.(496-498)aGa>aAa | p.R166K |
KIPAN | 9 | 133738356 | 133738356 | + | Silent | SNP | G | G | A | TCGA-CJ-4889-01A-01D-1373-10 | TCGA-CJ-4889-11A-01D-1373-10 | g.chr9:133738356G>A | c.756G>A | c.(754-756)caG>caA | p.Q252Q |
KIPAN | 9 | 133748274 | 133748274 | + | Missense_Mutation | SNP | A | A | G | TCGA-KM-8443-01A-11D-2310-10 | TCGA-KM-8443-10A-01D-2311-10 | g.chr9:133748274A>G | c.935A>G | c.(934-936)tAt>tGt | p.Y312C |
KIPAN | 9 | 133748371 | 133748371 | + | Silent | SNP | C | C | T | TCGA-B9-4114-01A-01D-1252-08 | TCGA-B9-4114-10A-01D-1252-08 | g.chr9:133748371C>T | c.1032C>T | c.(1030-1032)gcC>gcT | p.A344A |
KIPAN | 9 | 133748374 | 133748374 | + | Silent | SNP | T | T | C | TCGA-2Z-A9JD-01A-11D-A42J-10 | TCGA-2Z-A9JD-10A-01D-A42M-10 | g.chr9:133748374T>C | c.1035T>C | c.(1033-1035)acT>acC | p.T345T |
KIPAN | 9 | 133750263 | 133750263 | + | Missense_Mutation | SNP | C | C | T | TCGA-CJ-4920-01A-01D-1429-08 | TCGA-CJ-4920-11A-01D-1429-08 | g.chr9:133750263C>T | c.1094C>T | c.(1093-1095)gCt>gTt | p.A365V |
KIPAN | 9 | 133760875 | 133760875 | + | Silent | SNP | C | C | T | TCGA-BP-4998-01A-01D-1462-08 | TCGA-BP-4998-11A-01D-1462-08 | g.chr9:133760875C>T | c.3198C>T | c.(3196-3198)ttC>ttT | p.F1066F |
KIRC | 9 | 133729596 | 133729596 | + | Missense_Mutation | SNP | T | T | G | TCGA-B0-5696-01A-11D-1534-10 | TCGA-B0-5696-11A-01D-1534-10 | g.chr9:133729596T>G | c.225T>G | c.(223-225)agT>agG | p.S75R |
KIRC | 9 | 133730431 | 133730431 | + | Missense_Mutation | SNP | G | G | A | TCGA-BP-4159-01A-02D-1366-10 | TCGA-BP-4159-11A-01D-1366-10 | g.chr9:133730431G>A | c.497G>A | c.(496-498)aGa>aAa | p.R166K |
KIRC | 9 | 133738356 | 133738356 | + | Silent | SNP | G | G | A | TCGA-CJ-4889-01A-01D-1373-10 | TCGA-CJ-4889-11A-01D-1373-10 | g.chr9:133738356G>A | c.756G>A | c.(754-756)caG>caA | p.Q252Q |
KIRC | 9 | 133750263 | 133750263 | + | Missense_Mutation | SNP | C | C | T | TCGA-CJ-4920-01A-01D-1429-08 | TCGA-CJ-4920-11A-01D-1429-08 | g.chr9:133750263C>T | c.1094C>T | c.(1093-1095)gCt>gTt | p.A365V |
KIRC | 9 | 133760875 | 133760875 | + | Silent | SNP | C | C | T | TCGA-BP-4998-01A-01D-1462-08 | TCGA-BP-4998-11A-01D-1462-08 | g.chr9:133760875C>T | c.3198C>T | c.(3196-3198)ttC>ttT | p.F1066F |
KIRP | 9 | 133730265 | 133730265 | + | Missense_Mutation | SNP | G | G | C | TCGA-EV-5903-01A-11D-1589-08 | TCGA-EV-5903-10A-01D-1589-08 | g.chr9:133730265G>C | c.331G>C | c.(331-333)Gtc>Ctc | p.V111L |
KIRP | 9 | 133748371 | 133748371 | + | Silent | SNP | C | C | T | TCGA-B9-4114-01A-01D-1252-08 | TCGA-B9-4114-10A-01D-1252-08 | g.chr9:133748371C>T | c.1032C>T | c.(1030-1032)gcC>gcT | p.A344A |
KIRP | 9 | 133748374 | 133748374 | + | Silent | SNP | T | T | C | TCGA-2Z-A9JD-01A-11D-A42J-10 | TCGA-2Z-A9JD-10A-01D-A42M-10 | g.chr9:133748374T>C | c.1035T>C | c.(1033-1035)acT>acC | p.T345T |
LAML | 9 | 133760430 | 133760430 | + | Missense_Mutation | SNP | C | C | T | TCGA-AB-2999-03A-01D-0739-09 | TCGA-AB-2999-11A-01D-0739-09 | g.chr9:133760430C>T | c.2753C>T | c.(2752-2754)cCg>cTg | p.P918L |
LGG | 9 | 133729608 | 133729608 | + | Silent | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133729608T>G | c.237T>G | c.(235-237)acT>acG | p.T79T |
LGG | 9 | 133750263 | 133750263 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133750263C>A | c.1094C>A | c.(1093-1095)gCt>gAt | p.A365D |
LGG | 9 | 133753948 | 133753948 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133753948C>T | c.1417C>T | c.(1417-1419)Cga>Tga | p.R473* |
LGG | 9 | 133760330 | 133760330 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133760330C>T | c.2653C>T | c.(2653-2655)Cca>Tca | p.P885S |
LGG | 9 | 133761036 | 133761036 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:133761036C>T | c.3359C>T | c.(3358-3360)tCg>tTg | p.S1120L |
LIHC | 9 | 133759735 | 133759735 | + | Silent | SNP | G | G | C | TCGA-2Y-A9HB-01A-11D-A38X-10 | TCGA-2Y-A9HB-10A-01D-A38X-10 | g.chr9:133759735G>C | c.2058G>C | c.(2056-2058)ctG>ctC | p.L686L |
LIHC | 9 | 133759741 | 133759741 | + | Missense_Mutation | SNP | G | G | T | TCGA-2Y-A9HB-01A-11D-A38X-10 | TCGA-2Y-A9HB-10A-01D-A38X-10 | g.chr9:133759741G>T | c.2064G>T | c.(2062-2064)aaG>aaT | p.K688N |
LIHC | 9 | 133759994 | 133759995 | + | Frame_Shift_Del | DEL | GA | GA | - | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr9:133759994_133759995delGA | c.2317_2318delGA | c.(2317-2319)gacfs | p.D773fs |
LIHC | 9 | 133761037 | 133761037 | + | Silent | SNP | G | G | T | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr9:133761037G>T | c.3360G>T | c.(3358-3360)tcG>tcT | p.S1120S |
LUAD | 9 | 133730335 | 133730335 | + | Missense_Mutation | SNP | G | G | T | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chr9:133730335G>T | c.401G>T | c.(400-402)cGc>cTc | p.R134L |
LUAD | 9 | 133738212 | 133738212 | + | Silent | SNP | G | G | C | TCGA-99-8032-01A-11D-2238-08 | TCGA-99-8032-10A-01D-2238-08 | g.chr9:133738212G>C | c.612G>C | c.(610-612)acG>acC | p.T204T |
LUAD | 9 | 133738224 | 133738224 | + | Silent | SNP | G | G | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr9:133738224G>T | c.624G>T | c.(622-624)ggG>ggT | p.G208G |
LUAD | 9 | 133747590 | 133747590 | + | Silent | SNP | G | G | A | TCGA-99-8033-01A-11D-2238-08 | TCGA-99-8033-10A-01D-2238-08 | g.chr9:133747590G>A | c.897G>A | c.(895-897)gtG>gtA | p.V299V |
LUAD | 9 | 133753854 | 133753854 | + | Silent | SNP | G | G | A | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr9:133753854G>A | c.1323G>A | c.(1321-1323)ccG>ccA | p.P441P |
LUAD | 9 | 133759423 | 133759423 | + | Silent | SNP | C | C | A | TCGA-55-7576-01A-11D-2063-08 | TCGA-55-7576-10A-01D-2063-08 | g.chr9:133759423C>A | c.1746C>A | c.(1744-1746)ggC>ggA | p.G582G |
LUAD | 9 | 133759424 | 133759424 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-7576-01A-11D-2063-08 | TCGA-55-7576-10A-01D-2063-08 | g.chr9:133759424G>A | c.1747G>A | c.(1747-1749)Ggc>Agc | p.G583S |
LUAD | 9 | 133759490 | 133759492 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-44-7669-01A-21D-2063-08 | TCGA-44-7669-10A-01D-2063-08 | g.chr9:133759490_133759492delAAG | c.1813_1815delAAG | c.(1813-1815)aagdel | p.K609del |
LUAD | 9 | 133759490 | 133759492 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-49-4505-01A-01D-1931-08 | TCGA-49-4505-11A-01D-1265-08 | g.chr9:133759490_133759492delAAG | c.1813_1815delAAG | c.(1813-1815)aagdel | p.K609del |
LUAD | 9 | 133759670 | 133759671 | + | Missense_Mutation | DNP | GG | GG | TT | TCGA-67-4679-01B-01D-1753-08 | TCGA-67-4679-10A-01D-1753-08 | g.chr9:133759670_133759671GG>TT | c.1993_1994GG>TT | c.(1993-1995)GGg>TTg | p.G665L |
LUAD | 9 | 133760409 | 133760409 | + | Missense_Mutation | SNP | G | G | T | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr9:133760409G>T | c.2732G>T | c.(2731-2733)gGa>gTa | p.G911V |
LUAD | 9 | 133760560 | 133760560 | + | Silent | SNP | G | G | T | TCGA-93-8067-01A-11D-2284-08 | TCGA-93-8067-10A-01D-2284-08 | g.chr9:133760560G>T | c.2883G>T | c.(2881-2883)ccG>ccT | p.P961P |
LUAD | 9 | 133760589 | 133760589 | + | Missense_Mutation | SNP | C | C | T | TCGA-93-A4JN-01A-11D-A24P-08 | TCGA-93-A4JN-10A-01D-A24P-08 | g.chr9:133760589C>T | c.2912C>T | c.(2911-2913)cCg>cTg | p.P971L |
LUAD | 9 | 133760658 | 133760658 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-7669-01A-21D-2063-08 | TCGA-44-7669-10A-01D-2063-08 | g.chr9:133760658G>T | c.2981G>T | c.(2980-2982)gGg>gTg | p.G994V |
LUAD | 9 | 133760684 | 133760684 | + | Missense_Mutation | SNP | A | A | G | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr9:133760684A>G | c.3007A>G | c.(3007-3009)Atc>Gtc | p.I1003V |
LUAD | 9 | 133760830 | 133760830 | + | Silent | SNP | C | C | T | TCGA-73-7498-01A-12D-2184-08 | TCGA-73-7498-10A-01D-2184-08 | g.chr9:133760830C>T | c.3153C>T | c.(3151-3153)gcC>gcT | p.A1051A |
LUSC | 9 | 133750280 | 133750280 | + | Missense_Mutation | SNP | G | G | T | TCGA-39-5016-01A-01D-1441-08 | TCGA-39-5016-11A-01D-1441-08 | g.chr9:133750280G>T | c.1111G>T | c.(1111-1113)Gta>Tta | p.V371L |
LUSC | 9 | 133753888 | 133753888 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2786-01A-01D-1522-08 | TCGA-66-2786-11A-01D-1522-08 | g.chr9:133753888G>C | c.1357G>C | c.(1357-1359)Gag>Cag | p.E453Q |
LUSC | 9 | 133760253 | 133760253 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr9:133760253C>G | c.2576C>G | c.(2575-2577)tCa>tGa | p.S859* |
LUSC | 9 | 133760617 | 133760617 | + | Silent | SNP | C | C | A | TCGA-33-4532-01A-01D-1267-08 | TCGA-33-4532-11A-01D-1267-08 | g.chr9:133760617C>A | c.2940C>A | c.(2938-2940)ccC>ccA | p.P980P |
LUSC | 9 | 133760965 | 133760965 | + | Silent | SNP | G | G | A | TCGA-66-2754-01A-01D-0983-08 | TCGA-66-2754-11A-01D-0983-08 | g.chr9:133760965G>A | c.3288G>A | c.(3286-3288)gaG>gaA | p.E1096E |
OV | 9 | 133760930 | 133760930 | + | Missense_Mutation | SNP | G | G | C | TCGA-36-2534-01A-01D-1526-09 | TCGA-36-2534-10A-01D-1526-09 | g.chr9:133760930G>C | c.3253G>C | c.(3253-3255)Gag>Cag | p.E1085Q |
PAAD | 9 | 133730325 | 133730325 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:133730325C>T | c.391C>T | c.(391-393)Cct>Tct | p.P131S |
PAAD | 9 | 133755491 | 133755491 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:133755491C>A | c.1460C>A | c.(1459-1461)gCt>gAt | p.A487D |
PAAD | 9 | 133759474 | 133759474 | + | Missense_Mutation | SNP | G | G | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:133759474G>C | c.1797G>C | c.(1795-1797)ttG>ttC | p.L599F |
PAAD | 9 | 133760702 | 133760702 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:133760702C>T | c.3025C>T | c.(3025-3027)Cga>Tga | p.R1009* |
PAAD | 9 | 133760790 | 133760790 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:133760790C>T | c.3113C>T | c.(3112-3114)gCg>gTg | p.A1038V |
PRAD | 9 | 133738400 | 133738400 | + | Missense_Mutation | SNP | C | C | T | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr9:133738400C>T | c.800C>T | c.(799-801)aCg>aTg | p.T267M |
PRAD | 9 | 133753877 | 133753877 | + | Missense_Mutation | SNP | A | A | G | TCGA-HC-7209-01A-11D-2114-08 | TCGA-HC-7209-10A-01D-2115-08 | g.chr9:133753877A>G | c.1346A>G | c.(1345-1347)tAt>tGt | p.Y449C |
PRAD | 9 | 133759490 | 133759492 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-EJ-5531-01A-01D-1576-08 | TCGA-EJ-5531-10A-01D-1577-08 | g.chr9:133759490_133759492delAAG | c.1813_1815delAAG | c.(1813-1815)aagdel | p.K609del |
PRAD | 9 | 133759623 | 133759623 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr9:133759623delC | c.1946delC | c.(1945-1947)accfs | p.T649fs |
PRAD | 9 | 133760700 | 133760700 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr9:133760700C>T | c.3023C>T | c.(3022-3024)aCc>aTc | p.T1008I |
READ | 9 | 133729537 | 133729537 | + | Missense_Mutation | SNP | G | G | A | TCGA-AH-6644-01A-21D-1826-10 | TCGA-AH-6644-10A-01D-1826-10 | g.chr9:133729537G>A | c.166G>A | c.(166-168)Gct>Act | p.A56T |
READ | 9 | 133729569 | 133729569 | + | Silent | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:133729569C>T | c.198C>T | c.(196-198)ttC>ttT | p.F66F |
READ | 9 | 133730245 | 133730245 | + | Missense_Mutation | SNP | C | C | T | TCGA-DY-A0XA-01A-11D-A152-10 | TCGA-DY-A0XA-10A-01D-A152-10 | g.chr9:133730245C>T | c.311C>T | c.(310-312)aCc>aTc | p.T104I |
READ | 9 | 133748390 | 133748390 | + | Missense_Mutation | SNP | A | A | G | TCGA-EI-6508-01A-11D-1733-10 | TCGA-EI-6508-10A-01D-1733-10 | g.chr9:133748390A>G | c.1051A>G | c.(1051-1053)Atg>Gtg | p.M351V |
READ | 9 | 133760130 | 133760130 | + | Missense_Mutation | SNP | T | T | C | TCGA-EF-5830-01A-01D-1657-10 | TCGA-EF-5830-10A-01D-1657-10 | g.chr9:133760130T>C | c.2453T>C | c.(2452-2454)cTc>cCc | p.L818P |
SARC | 9 | 133738153 | 133738156 | + | Frame_Shift_Del | DEL | TACG | TACG | - | TCGA-DX-AB3C-01A-11D-A417-09 | TCGA-DX-AB3C-10A-01D-A41A-09 | g.chr9:133738153_133738156delTACG | c.553_556delTACG | c.(553-558)tacgtcfs | p.YV185fs |
SARC | 9 | 133750394 | 133750394 | + | Missense_Mutation | SNP | G | G | A | TCGA-QQ-A5VD-01A-21D-A32I-09 | TCGA-QQ-A5VD-10A-01D-A32I-09 | g.chr9:133750394G>A | c.1225G>A | c.(1225-1227)Gag>Aag | p.E409K |
SKCM | 9 | 133738217 | 133738217 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZF-06A-12D-A197-08 | TCGA-FS-A1ZF-10A-01D-A199-08 | g.chr9:133738217C>T | c.617C>T | c.(616-618)gCc>gTc | p.A206V |
SKCM | 9 | 133747523 | 133747523 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr9:133747523C>T | c.830C>T | c.(829-831)aCc>aTc | p.T277I |
SKCM | 9 | 133747600 | 133747600 | + | Splice_Site | SNP | G | G | A | TCGA-D9-A148-06A-11D-A19A-08 | TCGA-D9-A148-10A-01D-A19A-08 | g.chr9:133747600G>A | c.907G>A | c.(907-909)Ggg>Agg | p.G303R |
SKCM | 9 | 133748267 | 133748267 | + | Missense_Mutation | SNP | C | C | A | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr9:133748267C>A | c.928C>A | c.(928-930)Ccg>Acg | p.P310T |
SKCM | 9 | 133748268 | 133748268 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr9:133748268C>T | c.929C>T | c.(928-930)cCg>cTg | p.P310L |
SKCM | 9 | 133748382 | 133748382 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr9:133748382C>T | c.1043C>T | c.(1042-1044)tCg>tTg | p.S348L |
SKCM | 9 | 133755498 | 133755498 | + | Silent | SNP | C | C | T | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr9:133755498C>T | c.1467C>T | c.(1465-1467)atC>atT | p.I489I |
SKCM | 9 | 133755522 | 133755522 | + | Silent | SNP | C | C | T | TCGA-DA-A3F5-06A-11D-A20D-08 | TCGA-DA-A3F5-10A-01D-A20D-08 | g.chr9:133755522C>T | c.1491C>T | c.(1489-1491)ttC>ttT | p.F497F |
SKCM | 9 | 133755918 | 133755918 | + | Silent | SNP | C | C | T | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr9:133755918C>T | c.1545C>T | c.(1543-1545)gtC>gtT | p.V515V |
SKCM | 9 | 133755918 | 133755918 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZC-06A-11D-A197-08 | TCGA-FS-A1ZC-10A-01D-A199-08 | g.chr9:133755918C>T | c.1545C>T | c.(1543-1545)gtC>gtT | p.V515V |
SKCM | 9 | 133756025 | 133756025 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1YY-06A-11D-A197-08 | TCGA-FS-A1YY-10A-01D-A199-08 | g.chr9:133756025C>T | c.1652C>T | c.(1651-1653)cCt>cTt | p.P551L |
SKCM | 9 | 133759490 | 133759492 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-EE-A29G-06A-12D-A196-08 | TCGA-EE-A29G-10A-01D-A198-08 | g.chr9:133759490_133759492delAAG | c.1813_1815delAAG | c.(1813-1815)aagdel | p.K609del |
SKCM | 9 | 133759737 | 133759737 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-D3-A3C3-06A-12D-A19A-08 | TCGA-D3-A3C3-10A-01D-A19A-08 | g.chr9:133759737G>A | c.2060G>A | c.(2059-2061)tGg>tAg | p.W687* |
SKCM | 9 | 133759803 | 133759803 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A198-06A-11D-A196-08 | TCGA-ER-A198-10A-01D-A198-08 | g.chr9:133759803C>T | c.2126C>T | c.(2125-2127)tCc>tTc | p.S709F |
SKCM | 9 | 133759967 | 133759967 | + | Missense_Mutation | SNP | C | C | G | TCGA-ER-A2NE-06A-21D-A196-08 | TCGA-ER-A2NE-10A-01D-A198-08 | g.chr9:133759967C>G | c.2290C>G | c.(2290-2292)Cgg>Ggg | p.R764G |
SKCM | 9 | 133760068 | 133760068 | + | Silent | SNP | C | C | T | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr9:133760068C>T | c.2391C>T | c.(2389-2391)gtC>gtT | p.V797V |
SKCM | 9 | 133760199 | 133760199 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr9:133760199C>T | c.2522C>T | c.(2521-2523)gCc>gTc | p.A841V |
SKCM | 9 | 133760200 | 133760200 | + | Silent | SNP | C | C | T | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr9:133760200C>T | c.2523C>T | c.(2521-2523)gcC>gcT | p.A841A |
SKCM | 9 | 133760588 | 133760588 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr9:133760588C>T | c.2911C>T | c.(2911-2913)Ccg>Tcg | p.P971S |
SKCM | 9 | 133760622 | 133760622 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr9:133760622C>T | c.2945C>T | c.(2944-2946)cCc>cTc | p.P982L |
SKCM | 9 | 133760887 | 133760888 | + | Frame_Shift_Del | DEL | TG | TG | - | TCGA-FS-A4F9-06A-11D-A24R-08 | TCGA-FS-A4F9-10A-01D-A24R-08 | g.chr9:133760887_133760888delTG | c.3210_3211delTG | c.(3208-3213)tatgtgfs | p.V1071fs |