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 | 136648640 | 136648640 | + | Missense_Mutation | SNP | G | G | T | TCGA-OR-A5JA-01A-11D-A29I-10 | TCGA-OR-A5JA-10A-01D-A29L-10 | g.chr9:136648640G>T | c.1708C>A | c.(1708-1710)Cct>Act | p.P570T |
ACC | 9 | 136650966 | 136650966 | + | Silent | SNP | C | C | T | TCGA-OR-A5JQ-01A-11D-A29I-10 | TCGA-OR-A5JQ-10A-01D-A29L-10 | g.chr9:136650966C>T | c.1464G>A | c.(1462-1464)caG>caA | p.Q488Q |
BLCA | 9 | 136633664 | 136633664 | + | Missense_Mutation | SNP | C | C | T | TCGA-KQ-A41Q-01A-11D-A339-08 | TCGA-KQ-A41Q-10D-01D-A339-08 | g.chr9:136633664C>T | c.2489G>A | c.(2488-2490)cGa>cAa | p.R830Q |
BLCA | 9 | 136634579 | 136634579 | + | Silent | SNP | G | G | A | TCGA-GC-A3RB-01A-12D-A21Z-08 | TCGA-GC-A3RB-10A-01D-A21Z-08 | g.chr9:136634579G>A | c.2394C>T | c.(2392-2394)ctC>ctT | p.L798L |
BLCA | 9 | 136637093 | 136637093 | + | Missense_Mutation | SNP | G | G | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr9:136637093G>T | c.2211C>A | c.(2209-2211)ttC>ttA | p.F737L |
BLCA | 9 | 136653479 | 136653479 | + | Missense_Mutation | SNP | C | C | G | TCGA-CF-A47X-01A-31D-A23U-08 | TCGA-CF-A47X-10A-01D-A23U-08 | g.chr9:136653479C>G | c.1404G>C | c.(1402-1404)aaG>aaC | p.K468N |
BLCA | 9 | 136662855 | 136662855 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-A9ST-01A-11D-A42E-08 | TCGA-XF-A9ST-10A-01D-A42H-08 | g.chr9:136662855C>T | c.913G>A | c.(913-915)Gag>Aag | p.E305K |
BLCA | 9 | 136671208 | 136671208 | + | Silent | SNP | C | C | T | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chr9:136671208C>T | c.831G>A | c.(829-831)aaG>aaA | p.K277K |
BLCA | 9 | 136674200 | 136674200 | + | Missense_Mutation | SNP | C | C | T | TCGA-GU-A42P-01A-11D-A23U-08 | TCGA-GU-A42P-10A-01D-A23U-08 | g.chr9:136674200C>T | c.628G>A | c.(628-630)Gag>Aag | p.E210K |
BLCA | 9 | 136804249 | 136804249 | + | Silent | SNP | G | G | T | TCGA-DK-A1A5-01A-11D-A13W-08 | TCGA-DK-A1A5-10A-01D-A13W-08 | g.chr9:136804249G>T | c.297C>A | c.(295-297)ctC>ctA | p.L99L |
BLCA | 9 | 136804268 | 136804268 | + | Missense_Mutation | SNP | A | A | G | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr9:136804268A>G | c.278T>C | c.(277-279)cTg>cCg | p.L93P |
BLCA | 9 | 136804281 | 136804281 | + | Missense_Mutation | SNP | T | T | A | TCGA-UY-A9PA-01A-11D-A38G-08 | TCGA-UY-A9PA-10A-01D-A38J-08 | g.chr9:136804281T>A | c.265A>T | c.(265-267)Agg>Tgg | p.R89W |
BLCA | 9 | 136857251 | 136857251 | + | Silent | SNP | G | G | C | TCGA-UY-A78M-01A-21D-A34U-08 | TCGA-UY-A78M-10A-01D-A34X-08 | g.chr9:136857251G>C | c.150C>G | c.(148-150)ctC>ctG | p.L50L |
BLCA | 9 | 136857321 | 136857321 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9R7-01A-11D-A38G-08 | TCGA-ZF-A9R7-10A-01D-A38J-08 | g.chr9:136857321G>C | c.80C>G | c.(79-81)tCg>tGg | p.S27W |
BRCA | 9 | 136634607 | 136634607 | + | Missense_Mutation | SNP | T | T | C | TCGA-E2-A15J-01A-11D-A12Q-09 | TCGA-E2-A15J-10A-01D-A12Q-09 | g.chr9:136634607T>C | c.2366A>G | c.(2365-2367)aAc>aGc | p.N789S |
BRCA | 9 | 136635569 | 136635569 | + | Missense_Mutation | SNP | C | C | T | TCGA-AN-A0AK-01A-21W-A019-09 | TCGA-AN-A0AK-10A-01W-A021-09 | g.chr9:136635569C>T | c.2278G>A | c.(2278-2280)Gac>Aac | p.D760N |
BRCA | 9 | 136649470 | 136649470 | + | Missense_Mutation | SNP | T | T | G | TCGA-D8-A1JD-01A-11D-A13L-09 | TCGA-D8-A1JD-10A-01D-A13O-09 | g.chr9:136649470T>G | c.1603A>C | c.(1603-1605)Acc>Ccc | p.T535P |
BRCA | 9 | 136661557 | 136661557 | + | Silent | SNP | G | G | C | TCGA-E2-A1IN-01A-11D-A13L-09 | TCGA-E2-A1IN-10A-01D-A188-09 | g.chr9:136661557G>C | c.1026C>G | c.(1024-1026)ctC>ctG | p.L342L |
CESC | 9 | 136641167 | 136641167 | + | Missense_Mutation | SNP | G | G | T | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr9:136641167G>T | c.2001C>A | c.(1999-2001)gaC>gaA | p.D667E |
CESC | 9 | 136649441 | 136649441 | + | Silent | SNP | G | G | C | TCGA-C5-A2M1-01A-11D-A18J-09 | TCGA-C5-A2M1-10A-01D-A18J-09 | g.chr9:136649441G>C | c.1632C>G | c.(1630-1632)ctC>ctG | p.L544L |
CESC | 9 | 136652376 | 136652376 | + | Missense_Mutation | SNP | C | C | T | TCGA-EA-A3HQ-01A-11D-A20U-09 | TCGA-EA-A3HQ-10A-01D-A20U-09 | g.chr9:136652376C>T | c.1414G>A | c.(1414-1416)Ggg>Agg | p.G472R |
CESC | 9 | 136857230 | 136857230 | + | Silent | SNP | G | G | C | TCGA-EK-A2RK-01A-11D-A18J-09 | TCGA-EK-A2RK-10A-01D-A18J-09 | g.chr9:136857230G>C | c.171C>G | c.(169-171)ctC>ctG | p.L57L |
CESC | 9 | 136857321 | 136857321 | + | Missense_Mutation | SNP | G | G | C | TCGA-EK-A2RK-01A-11D-A18J-09 | TCGA-EK-A2RK-10A-01D-A18J-09 | g.chr9:136857321G>C | c.80C>G | c.(79-81)tCg>tGg | p.S27W |
COAD | 9 | 136633570 | 136633570 | + | Silent | SNP | G | G | A | TCGA-AA-3994-01A-01W-1073-09 | TCGA-AA-3994-10A-01W-1073-09 | g.chr9:136633570G>A | c.2583C>T | c.(2581-2583)aaC>aaT | p.N861N |
COAD | 9 | 136633575 | 136633575 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr9:136633575T>C | c.2578A>G | c.(2578-2580)Acc>Gcc | p.T860A |
COAD | 9 | 136633630 | 136633630 | + | Silent | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr9:136633630G>A | c.2523C>T | c.(2521-2523)gaC>gaT | p.D841D |
COAD | 9 | 136633692 | 136633692 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr9:136633692C>A | c.2461G>T | c.(2461-2463)Gct>Tct | p.A821S |
COAD | 9 | 136635569 | 136635569 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr9:136635569C>T | c.2278G>A | c.(2278-2280)Gac>Aac | p.D760N |
COAD | 9 | 136637120 | 136637120 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3534-01A-01W-0831-10 | TCGA-AA-3534-10A-01W-0831-10 | g.chr9:136637120C>A | c.2184G>T | c.(2182-2184)tgG>tgT | p.W728C |
COAD | 9 | 136637156 | 136637156 | + | Missense_Mutation | SNP | C | C | A | TCGA-D5-6533-01A-11D-1719-10 | TCGA-D5-6533-10A-01D-1719-10 | g.chr9:136637156C>A | c.2148G>T | c.(2146-2148)gaG>gaT | p.E716D |
COAD | 9 | 136637156 | 136637156 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6626-01A-11D-1771-10 | TCGA-G4-6626-10A-01D-1771-10 | g.chr9:136637156C>A | c.2148G>T | c.(2146-2148)gaG>gaT | p.E716D |
COAD | 9 | 136637156 | 136637156 | + | Silent | SNP | C | C | T | TCGA-G4-6307-01A-11D-1719-10 | TCGA-G4-6307-10A-01D-1720-10 | g.chr9:136637156C>T | c.2148G>A | c.(2146-2148)gaG>gaA | p.E716E |
COAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr9:136637157T>A | c.2147A>T | c.(2146-2148)gAg>gTg | p.E716V |
COAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | A | TCGA-D5-6536-01A-11D-1719-10 | TCGA-D5-6536-10A-01D-1719-10 | g.chr9:136637157T>A | c.2147A>T | c.(2146-2148)gAg>gTg | p.E716V |
COAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chr9:136637157T>C | c.2147A>G | c.(2146-2148)gAg>gGg | p.E716G |
COAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6537-01A-11D-1719-10 | TCGA-D5-6537-10A-01D-1719-10 | g.chr9:136637157T>C | c.2147A>G | c.(2146-2148)gAg>gGg | p.E716G |
COAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr9:136637157T>C | c.2147A>G | c.(2146-2148)gAg>gGg | p.E716G |
COAD | 9 | 136637158 | 136637158 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr9:136637158C>T | c.2146G>A | c.(2146-2148)Gag>Aag | p.E716K |
COAD | 9 | 136637158 | 136637158 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CK-4947-01B-11D-1650-10 | TCGA-CK-4947-10A-01D-1650-10 | g.chr9:136637158C>A | c.2146G>T | c.(2146-2148)Gag>Tag | p.E716* |
COAD | 9 | 136640093 | 136640093 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr9:136640093C>T | c.2099G>A | c.(2098-2100)cGg>cAg | p.R700Q |
COAD | 9 | 136640122 | 136640122 | + | Silent | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr9:136640122G>A | c.2070C>T | c.(2068-2070)caC>caT | p.H690H |
COAD | 9 | 136641199 | 136641199 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr9:136641199G>A | c.1969C>T | c.(1969-1971)Ccc>Tcc | p.P657S |
COAD | 9 | 136650980 | 136650980 | + | Missense_Mutation | SNP | G | G | T | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr9:136650980G>T | c.1450C>A | c.(1450-1452)Ctt>Att | p.L484I |
COAD | 9 | 136726543 | 136726543 | + | Silent | SNP | C | C | A | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr9:136726543C>A | c.333G>T | c.(331-333)gcG>gcT | p.A111A |
COAD | 9 | 136804243 | 136804243 | + | Silent | SNP | A | A | G | TCGA-AZ-5407-01A-01D-1719-10 | TCGA-AZ-5407-10A-01D-1719-10 | g.chr9:136804243A>G | c.303T>C | c.(301-303)gaT>gaC | p.D101D |
COAD | 9 | 136804245 | 136804245 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6541-01A-11D-1719-10 | TCGA-D5-6541-10A-01D-1719-10 | g.chr9:136804245C>T | c.301G>A | c.(301-303)Gat>Aat | p.D101N |
COAD | 9 | 136804319 | 136804319 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr9:136804319C>T | c.227G>A | c.(226-228)cGc>cAc | p.R76H |
COADREAD | 9 | 136633570 | 136633570 | + | Silent | SNP | G | G | A | TCGA-AA-3994-01A-01W-1073-09 | TCGA-AA-3994-10A-01W-1073-09 | g.chr9:136633570G>A | c.2583C>T | c.(2581-2583)aaC>aaT | p.N861N |
COADREAD | 9 | 136633575 | 136633575 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr9:136633575T>C | c.2578A>G | c.(2578-2580)Acc>Gcc | p.T860A |
COADREAD | 9 | 136633630 | 136633630 | + | Silent | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr9:136633630G>A | c.2523C>T | c.(2521-2523)gaC>gaT | p.D841D |
COADREAD | 9 | 136633646 | 136633646 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:136633646G>A | c.2507C>T | c.(2506-2508)tCg>tTg | p.S836L |
COADREAD | 9 | 136633692 | 136633692 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr9:136633692C>A | c.2461G>T | c.(2461-2463)Gct>Tct | p.A821S |
COADREAD | 9 | 136635569 | 136635569 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr9:136635569C>T | c.2278G>A | c.(2278-2280)Gac>Aac | p.D760N |
COADREAD | 9 | 136637120 | 136637120 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3534-01A-01W-0831-10 | TCGA-AA-3534-10A-01W-0831-10 | g.chr9:136637120C>A | c.2184G>T | c.(2182-2184)tgG>tgT | p.W728C |
COADREAD | 9 | 136637156 | 136637156 | + | Missense_Mutation | SNP | C | C | A | TCGA-D5-6533-01A-11D-1719-10 | TCGA-D5-6533-10A-01D-1719-10 | g.chr9:136637156C>A | c.2148G>T | c.(2146-2148)gaG>gaT | p.E716D |
COADREAD | 9 | 136637156 | 136637156 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6626-01A-11D-1771-10 | TCGA-G4-6626-10A-01D-1771-10 | g.chr9:136637156C>A | c.2148G>T | c.(2146-2148)gaG>gaT | p.E716D |
COADREAD | 9 | 136637156 | 136637156 | + | Silent | SNP | C | C | T | TCGA-G4-6307-01A-11D-1719-10 | TCGA-G4-6307-10A-01D-1720-10 | g.chr9:136637156C>T | c.2148G>A | c.(2146-2148)gaG>gaA | p.E716E |
COADREAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr9:136637157T>A | c.2147A>T | c.(2146-2148)gAg>gTg | p.E716V |
COADREAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | A | TCGA-D5-6536-01A-11D-1719-10 | TCGA-D5-6536-10A-01D-1719-10 | g.chr9:136637157T>A | c.2147A>T | c.(2146-2148)gAg>gTg | p.E716V |
COADREAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chr9:136637157T>C | c.2147A>G | c.(2146-2148)gAg>gGg | p.E716G |
COADREAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6537-01A-11D-1719-10 | TCGA-D5-6537-10A-01D-1719-10 | g.chr9:136637157T>C | c.2147A>G | c.(2146-2148)gAg>gGg | p.E716G |
COADREAD | 9 | 136637157 | 136637157 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr9:136637157T>C | c.2147A>G | c.(2146-2148)gAg>gGg | p.E716G |
COADREAD | 9 | 136637158 | 136637158 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr9:136637158C>T | c.2146G>A | c.(2146-2148)Gag>Aag | p.E716K |
COADREAD | 9 | 136637158 | 136637158 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CK-4947-01B-11D-1650-10 | TCGA-CK-4947-10A-01D-1650-10 | g.chr9:136637158C>A | c.2146G>T | c.(2146-2148)Gag>Tag | p.E716* |
COADREAD | 9 | 136640093 | 136640093 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr9:136640093C>T | c.2099G>A | c.(2098-2100)cGg>cAg | p.R700Q |
COADREAD | 9 | 136640122 | 136640122 | + | Silent | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr9:136640122G>A | c.2070C>T | c.(2068-2070)caC>caT | p.H690H |
COADREAD | 9 | 136641199 | 136641199 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr9:136641199G>A | c.1969C>T | c.(1969-1971)Ccc>Tcc | p.P657S |
COADREAD | 9 | 136642532 | 136642532 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr9:136642532C>A | c.1944G>T | c.(1942-1944)aaG>aaT | p.K648N |
COADREAD | 9 | 136650980 | 136650980 | + | Missense_Mutation | SNP | G | G | T | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr9:136650980G>T | c.1450C>A | c.(1450-1452)Ctt>Att | p.L484I |
COADREAD | 9 | 136726543 | 136726543 | + | Silent | SNP | C | C | A | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr9:136726543C>A | c.333G>T | c.(331-333)gcG>gcT | p.A111A |
COADREAD | 9 | 136804243 | 136804243 | + | Silent | SNP | A | A | G | TCGA-AZ-5407-01A-01D-1719-10 | TCGA-AZ-5407-10A-01D-1719-10 | g.chr9:136804243A>G | c.303T>C | c.(301-303)gaT>gaC | p.D101D |
COADREAD | 9 | 136804245 | 136804245 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6541-01A-11D-1719-10 | TCGA-D5-6541-10A-01D-1719-10 | g.chr9:136804245C>T | c.301G>A | c.(301-303)Gat>Aat | p.D101N |
COADREAD | 9 | 136804319 | 136804319 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr9:136804319C>T | c.227G>A | c.(226-228)cGc>cAc | p.R76H |
DLBC | 9 | 136640122 | 136640122 | + | Silent | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr9:136640122G>A | c.2070C>T | c.(2068-2070)caC>caT | p.H690H |
ESCA | 9 | 136662837 | 136662837 | + | Missense_Mutation | SNP | C | C | T | TCGA-IC-A6RE-01A-11D-A33E-09 | TCGA-IC-A6RE-10A-01D-A33H-09 | g.chr9:136662837C>T | c.931G>A | c.(931-933)Gtc>Atc | p.V311I |
ESCA | 9 | 136671268 | 136671268 | + | Silent | SNP | G | G | T | TCGA-L5-A4OJ-01A-11D-A27G-09 | TCGA-L5-A4OJ-11A-12D-A27G-09 | g.chr9:136671268G>T | c.771C>A | c.(769-771)gcC>gcA | p.A257A |
ESCA | 9 | 136726534 | 136726534 | + | Silent | SNP | C | C | T | TCGA-L5-A43J-01A-12D-A247-09 | TCGA-L5-A43J-11A-11D-A247-09 | g.chr9:136726534C>T | c.342G>A | c.(340-342)agG>agA | p.R114R |
GBM | 9 | 136653541 | 136653541 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0174-01A-01D-1491-08 | TCGA-06-0174-10B-01D-1491-08 | g.chr9:136653541C>T | c.1342G>A | c.(1342-1344)Gag>Aag | p.E448K |
GBM | 9 | 136656960 | 136656960 | + | Missense_Mutation | SNP | C | C | T | TCGA-32-4719-01A-01D-1353-08 | TCGA-32-4719-10A-01D-1353-08 | g.chr9:136656960C>T | c.1133G>A | c.(1132-1134)cGg>cAg | p.R378Q |
GBMLGG | 9 | 136641200 | 136641200 | + | Silent | SNP | C | C | T | TCGA-FG-A4MY-01A-11D-A26M-08 | TCGA-FG-A4MY-10A-01D-A26K-08 | g.chr9:136641200C>T | c.1968G>A | c.(1966-1968)ccG>ccA | p.P656P |
GBMLGG | 9 | 136648690 | 136648691 | + | Frame_Shift_Ins | INS | - | - | TG | TCGA-FG-A87N-01A-11D-A36O-08 | TCGA-FG-A87N-10A-01D-A367-08 | g.chr9:136648690_136648691insTG | c.1657_1658insCA | c.(1657-1659)atgfs | p.M553fs |
GBMLGG | 9 | 136653541 | 136653541 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0174-01A-01D-1491-08 | TCGA-06-0174-10B-01D-1491-08 | g.chr9:136653541C>T | c.1342G>A | c.(1342-1344)Gag>Aag | p.E448K |
GBMLGG | 9 | 136656960 | 136656960 | + | Missense_Mutation | SNP | C | C | T | TCGA-32-4719-01A-01D-1353-08 | TCGA-32-4719-10A-01D-1353-08 | g.chr9:136656960C>T | c.1133G>A | c.(1132-1134)cGg>cAg | p.R378Q |
GBMLGG | 9 | 136661642 | 136661642 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:136661642C>T | c.941G>A | c.(940-942)tGc>tAc | p.C314Y |
HNSC | 9 | 136629201 | 136629201 | + | Missense_Mutation | SNP | C | C | T | TCGA-CR-6481-01A-11D-1870-08 | TCGA-CR-6481-10A-01D-1870-08 | g.chr9:136629201C>T | c.2620G>A | c.(2620-2622)Gag>Aag | p.E874K |
HNSC | 9 | 136633698 | 136633698 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-A6JD-01A-11D-A31L-08 | TCGA-CV-A6JD-10A-01D-A31J-08 | g.chr9:136633698C>T | c.2455G>A | c.(2455-2457)Ggc>Agc | p.G819S |
HNSC | 9 | 136635537 | 136635537 | + | Silent | SNP | C | C | A | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr9:136635537C>A | c.2310G>T | c.(2308-2310)cgG>cgT | p.R770R |
HNSC | 9 | 136643922 | 136643922 | + | Missense_Mutation | SNP | C | C | G | TCGA-P3-A5QF-01A-11D-A28R-08 | TCGA-P3-A5QF-10A-01D-A28U-08 | g.chr9:136643922C>G | c.1852G>C | c.(1852-1854)Gag>Cag | p.E618Q |
HNSC | 9 | 136671217 | 136671217 | + | Silent | SNP | G | G | A | TCGA-CV-5444-01A-02D-1512-08 | TCGA-CV-5444-11A-01D-1512-08 | g.chr9:136671217G>A | c.822C>T | c.(820-822)ctC>ctT | p.L274L |
HNSC | 9 | 136671256 | 136671256 | + | Silent | SNP | G | G | A | TCGA-IQ-A61O-01A-11D-A30E-08 | TCGA-IQ-A61O-10A-01D-A30H-08 | g.chr9:136671256G>A | c.783C>T | c.(781-783)tcC>tcT | p.S261S |
HNSC | 9 | 136726538 | 136726538 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-A63U-01A-11D-A30E-08 | TCGA-CN-A63U-10A-01D-A30H-08 | g.chr9:136726538G>C | c.338C>G | c.(337-339)tCg>tGg | p.S113W |
KIPAN | 9 | 136633699 | 136633699 | + | Missense_Mutation | SNP | G | G | C | TCGA-CZ-4857-01A-01D-1373-10 | TCGA-CZ-4857-11A-01D-1373-10 | g.chr9:136633699G>C | c.2454C>G | c.(2452-2454)atC>atG | p.I818M |
KIPAN | 9 | 136642527 | 136642527 | + | Missense_Mutation | SNP | C | C | T | TCGA-A3-3373-01A-02D-1421-08 | TCGA-A3-3373-11A-01D-1421-08 | g.chr9:136642527C>T | c.1949G>A | c.(1948-1950)tGc>tAc | p.C650Y |
KIPAN | 9 | 136674238 | 136674238 | + | Missense_Mutation | SNP | T | T | A | TCGA-CZ-5989-01A-11D-1669-08 | TCGA-CZ-5989-11A-01D-1669-08 | g.chr9:136674238T>A | c.590A>T | c.(589-591)gAc>gTc | p.D197V |
KIRC | 9 | 136633699 | 136633699 | + | Missense_Mutation | SNP | G | G | C | TCGA-CZ-4857-01A-01D-1373-10 | TCGA-CZ-4857-11A-01D-1373-10 | g.chr9:136633699G>C | c.2454C>G | c.(2452-2454)atC>atG | p.I818M |
KIRC | 9 | 136642527 | 136642527 | + | Missense_Mutation | SNP | C | C | T | TCGA-A3-3373-01A-02D-1421-08 | TCGA-A3-3373-11A-01D-1421-08 | g.chr9:136642527C>T | c.1949G>A | c.(1948-1950)tGc>tAc | p.C650Y |
KIRC | 9 | 136674238 | 136674238 | + | Missense_Mutation | SNP | T | T | A | TCGA-CZ-5989-01A-11D-1669-08 | TCGA-CZ-5989-11A-01D-1669-08 | g.chr9:136674238T>A | c.590A>T | c.(589-591)gAc>gTc | p.D197V |
LGG | 9 | 136641200 | 136641200 | + | Silent | SNP | C | C | T | TCGA-FG-A4MY-01A-11D-A26M-08 | TCGA-FG-A4MY-10A-01D-A26K-08 | g.chr9:136641200C>T | c.1968G>A | c.(1966-1968)ccG>ccA | p.P656P |
LGG | 9 | 136648690 | 136648691 | + | Frame_Shift_Ins | INS | - | - | TG | TCGA-FG-A87N-01A-11D-A36O-08 | TCGA-FG-A87N-10A-01D-A367-08 | g.chr9:136648690_136648691insTG | c.1657_1658insCA | c.(1657-1659)atgfs | p.M553fs |
LGG | 9 | 136661642 | 136661642 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:136661642C>T | c.941G>A | c.(940-942)tGc>tAc | p.C314Y |
LUAD | 9 | 136633629 | 136633629 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-5778-01A-01D-1625-08 | TCGA-64-5778-10A-01D-1625-08 | g.chr9:136633629C>A | c.2524G>T | c.(2524-2526)Gtg>Ttg | p.V842L |
LUAD | 9 | 136633700 | 136633700 | + | Missense_Mutation | SNP | A | A | G | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr9:136633700A>G | c.2453T>C | c.(2452-2454)aTc>aCc | p.I818T |
LUAD | 9 | 136642532 | 136642532 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-7150-01A-21D-2036-08 | TCGA-78-7150-10A-01D-2036-08 | g.chr9:136642532C>A | c.1944G>T | c.(1942-1944)aaG>aaT | p.K648N |
LUAD | 9 | 136649542 | 136649542 | + | Splice_Site | SNP | T | T | G | TCGA-99-8028-01A-11D-2238-08 | TCGA-99-8028-10A-01D-2238-08 | g.chr9:136649542T>G | | c.e18-2 | |
LUAD | 9 | 136650949 | 136650949 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8358-01A-11D-2323-08 | TCGA-86-8358-10A-01D-2323-08 | g.chr9:136650949C>A | c.1481G>T | c.(1480-1482)tGc>tTc | p.C494F |
LUAD | 9 | 136654437 | 136654437 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-A4DG-01A-11D-A24D-08 | TCGA-55-A4DG-10A-01D-A24F-08 | g.chr9:136654437G>C | c.1217C>G | c.(1216-1218)cCa>cGa | p.P406R |
LUAD | 9 | 136656922 | 136656922 | + | Missense_Mutation | SNP | T | T | A | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr9:136656922T>A | c.1171A>T | c.(1171-1173)Agt>Tgt | p.S391C |
LUAD | 9 | 136804229 | 136804229 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-95-A4VN-01A-11D-A25L-08 | TCGA-95-A4VN-10A-01D-A25L-08 | g.chr9:136804229delC | c.317delG | c.(316-318)ggafs | p.G106fs |
LUSC | 9 | 136635533 | 136635533 | + | Missense_Mutation | SNP | G | G | A | TCGA-39-5030-01A-01D-1441-08 | TCGA-39-5030-11A-01D-1441-08 | g.chr9:136635533G>A | c.2314C>T | c.(2314-2316)Cgt>Tgt | p.R772C |
LUSC | 9 | 136661648 | 136661648 | + | Splice_Site | SNP | T | T | A | TCGA-18-3412-01A-01D-0983-08 | TCGA-18-3412-11A-01D-0983-08 | g.chr9:136661648T>A | | c.e11-2 | |
LUSC | 9 | 136662858 | 136662858 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2742-01A-01D-0983-08 | TCGA-66-2742-11A-01D-0983-08 | g.chr9:136662858G>C | c.910C>G | c.(910-912)Cgg>Ggg | p.R304G |
LUSC | 9 | 136662864 | 136662864 | + | Missense_Mutation | SNP | C | C | T | TCGA-37-3783-01A-01D-1267-08 | TCGA-37-3783-10A-01D-1267-08 | g.chr9:136662864C>T | c.904G>A | c.(904-906)Gcc>Acc | p.A302T |
LUSC | 9 | 136671274 | 136671274 | + | Silent | SNP | C | C | T | TCGA-33-4547-01A-01D-1267-08 | TCGA-33-4547-11A-01D-1267-08 | g.chr9:136671274C>T | c.765G>A | c.(763-765)ctG>ctA | p.L255L |
LUSC | 9 | 136726513 | 136726513 | + | Silent | SNP | C | C | A | TCGA-66-2742-01A-01D-0983-08 | TCGA-66-2742-11A-01D-0983-08 | g.chr9:136726513C>A | c.363G>T | c.(361-363)gcG>gcT | p.A121A |
OV | 9 | 136640099 | 136640099 | + | Missense_Mutation | SNP | C | C | A | TCGA-13-2065-01A-01D-1526-09 | TCGA-13-2065-10A-01D-1526-09 | g.chr9:136640099C>A | c.2093G>T | c.(2092-2094)aGg>aTg | p.R698M |
OV | 9 | 136656967 | 136656967 | + | Missense_Mutation | SNP | C | C | A | TCGA-25-1315-01A-01W-0494-09 | TCGA-25-1315-10A-01W-0494-09 | g.chr9:136656967C>A | c.1126G>T | c.(1126-1128)Gtt>Ttt | p.V376F |
OV | 9 | 136661570 | 136661570 | + | Missense_Mutation | SNP | T | T | A | TCGA-29-1764-01A-01W-0633-09 | TCGA-29-1764-10A-01W-0634-09 | g.chr9:136661570T>A | c.1013A>T | c.(1012-1014)aAa>aTa | p.K338I |
OV | 9 | 136726544 | 136726544 | + | Missense_Mutation | SNP | G | G | A | TCGA-09-0369-01A-01W-0372-09 | TCGA-09-0369-10C-01W-0372-09 | g.chr9:136726544G>A | c.332C>T | c.(331-333)gCg>gTg | p.A111V |
PRAD | 9 | 136634554 | 136634554 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr9:136634554C>T | c.2419G>A | c.(2419-2421)Gct>Act | p.A807T |
PRAD | 9 | 136641200 | 136641200 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr9:136641200C>T | c.1968G>A | c.(1966-1968)ccG>ccA | p.P656P |
PRAD | 9 | 136642579 | 136642579 | + | Missense_Mutation | SNP | G | G | C | TCGA-M7-A71Y-01A-22D-A32B-08 | TCGA-M7-A71Y-10A-01D-A329-08 | g.chr9:136642579G>C | c.1897C>G | c.(1897-1899)Ctg>Gtg | p.L633V |
PRAD | 9 | 136857224 | 136857224 | + | Missense_Mutation | SNP | G | G | T | TCGA-J4-A6M7-01A-11D-A31L-08 | TCGA-J4-A6M7-10A-01D-A31J-08 | g.chr9:136857224G>T | c.177C>A | c.(175-177)gaC>gaA | p.D59E |
READ | 9 | 136633646 | 136633646 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:136633646G>A | c.2507C>T | c.(2506-2508)tCg>tTg | p.S836L |
READ | 9 | 136642532 | 136642532 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr9:136642532C>A | c.1944G>T | c.(1942-1944)aaG>aaT | p.K648N |
SARC | 9 | 136634550 | 136634550 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr9:136634550G>A | c.2423C>T | c.(2422-2424)cCc>cTc | p.P808L |
SARC | 9 | 136634551 | 136634551 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr9:136634551G>A | c.2422C>T | c.(2422-2424)Ccc>Tcc | p.P808S |
SARC | 9 | 136857268 | 136857268 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-Z4-A9VC-01A-11D-A37C-09 | TCGA-Z4-A9VC-10A-01D-A37F-09 | g.chr9:136857268G>A | c.133C>T | c.(133-135)Cag>Tag | p.Q45* |
SKCM | 9 | 136635505 | 136635505 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr9:136635505G>A | c.2342C>T | c.(2341-2343)tCc>tTc | p.S781F |
SKCM | 9 | 136637129 | 136637129 | + | Silent | SNP | C | C | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr9:136637129C>T | c.2175G>A | c.(2173-2175)aaG>aaA | p.K725K |
SKCM | 9 | 136641194 | 136641194 | + | Silent | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr9:136641194G>A | c.1974C>T | c.(1972-1974)atC>atT | p.I658I |
SKCM | 9 | 136645046 | 136645046 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GL-06A-11D-A196-08 | TCGA-EE-A2GL-10A-01D-A198-08 | g.chr9:136645046C>T | c.1756G>A | c.(1756-1758)Gga>Aga | p.G586R |
SKCM | 9 | 136650974 | 136650974 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-FS-A1ZW-06A-12D-A197-08 | TCGA-FS-A1ZW-10A-01D-A199-08 | g.chr9:136650974C>A | c.1456G>T | c.(1456-1458)Gga>Tga | p.G486* |
SKCM | 9 | 136654406 | 136654406 | + | Silent | SNP | G | G | A | TCGA-EE-A3AB-06A-11D-A196-08 | TCGA-EE-A3AB-10A-01D-A198-08 | g.chr9:136654406G>A | c.1248C>T | c.(1246-1248)tcC>tcT | p.S416S |
SKCM | 9 | 136661588 | 136661588 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr9:136661588G>A | c.995C>T | c.(994-996)cCc>cTc | p.P332L |
SKCM | 9 | 136661589 | 136661589 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr9:136661589G>A | c.994C>T | c.(994-996)Ccc>Tcc | p.P332S |