| 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 | 131346591 | 131346591 | + | Missense_Mutation | SNP | C | C | T | TCGA-PK-A5HB-01A-11D-A29I-10 | TCGA-PK-A5HB-11A-11D-A29L-10 | g.chr9:131346591C>T | c.2224C>T | c.(2224-2226)Cgc>Tgc | p.R742C |
| ACC | 9 | 131371246 | 131371246 | + | Missense_Mutation | SNP | G | G | T | TCGA-OR-A5JH-01A-11D-A30A-10 | TCGA-OR-A5JH-10A-01D-A30A-10 | g.chr9:131371246G>T | c.4585G>T | c.(4585-4587)Gtc>Ttc | p.V1529F |
| ACC | 9 | 131395498 | 131395498 | + | Missense_Mutation | SNP | G | G | A | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr9:131395498G>A | c.7304G>A | c.(7303-7305)cGg>cAg | p.R2435Q |
| BLCA | 9 | 131329130 | 131329130 | + | Silent | SNP | T | T | C | TCGA-DK-A1A7-01A-11D-A13W-08 | TCGA-DK-A1A7-10A-01D-A13W-08 | g.chr9:131329130T>C | c.111T>C | c.(109-111)cgT>cgC | p.R37R |
| BLCA | 9 | 131337056 | 131337056 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CF-A47S-01A-11D-A23U-08 | TCGA-CF-A47S-10A-01D-A23U-08 | g.chr9:131337056C>T | c.466C>T | c.(466-468)Cga>Tga | p.R156* |
| BLCA | 9 | 131339209 | 131339209 | + | Silent | SNP | G | G | T | TCGA-FD-A43N-01A-11D-A23U-08 | TCGA-FD-A43N-10A-01D-A23U-08 | g.chr9:131339209G>T | c.759G>T | c.(757-759)ggG>ggT | p.G253G |
| BLCA | 9 | 131339475 | 131339475 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CF-A9FF-01A-11D-A38G-08 | TCGA-CF-A9FF-10A-01D-A38J-08 | g.chr9:131339475C>T | c.853C>T | c.(853-855)Cga>Tga | p.R285* |
| BLCA | 9 | 131339520 | 131339520 | + | Silent | SNP | C | C | T | TCGA-ZF-AA54-01A-11D-A391-08 | TCGA-ZF-AA54-10A-01D-A394-08 | g.chr9:131339520C>T | c.898C>T | c.(898-900)Ctg>Ttg | p.L300L |
| BLCA | 9 | 131339534 | 131339535 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-CF-A9FH-01A-11D-A38G-08 | TCGA-CF-A9FH-10A-01D-A38J-08 | g.chr9:131339534_131339535insG | c.912_913insG | c.(913-915)gctfs | p.A305fs |
| BLCA | 9 | 131339779 | 131339779 | + | Missense_Mutation | SNP | C | C | T | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr9:131339779C>T | c.1079C>T | c.(1078-1080)tCa>tTa | p.S360L |
| BLCA | 9 | 131340465 | 131340465 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-G2-A3IE-01A-11D-A20D-08 | TCGA-G2-A3IE-10A-01D-A20D-08 | g.chr9:131340465G>T | c.1162G>T | c.(1162-1164)Gag>Tag | p.E388* |
| BLCA | 9 | 131340512 | 131340512 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-4Z-AA7O-01A-31D-A391-08 | TCGA-4Z-AA7O-10A-01D-A394-08 | g.chr9:131340512delC | c.1209delC | c.(1207-1209)cacfs | p.H403fs |
| BLCA | 9 | 131341958 | 131341958 | + | Missense_Mutation | SNP | G | G | A | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr9:131341958G>A | c.1264G>A | c.(1264-1266)Gaa>Aaa | p.E422K |
| BLCA | 9 | 131342000 | 131342000 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr9:131342000G>C | c.1306G>C | c.(1306-1308)Gat>Cat | p.D436H |
| BLCA | 9 | 131342008 | 131342008 | + | Silent | SNP | G | G | A | TCGA-DK-A3IS-01A-21D-A21A-08 | TCGA-DK-A3IS-10A-01D-A21A-08 | g.chr9:131342008G>A | c.1314G>A | c.(1312-1314)gtG>gtA | p.V438V |
| BLCA | 9 | 131343206 | 131343206 | + | Silent | SNP | C | C | T | TCGA-GD-A76B-01A-11D-A32B-08 | TCGA-GD-A76B-10A-01D-A329-08 | g.chr9:131343206C>T | c.1329C>T | c.(1327-1329)acC>acT | p.T443T |
| BLCA | 9 | 131345392 | 131345392 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-4Z-AA87-01A-11D-A391-08 | TCGA-4Z-AA87-10A-01D-A394-08 | g.chr9:131345392C>T | c.1843C>T | c.(1843-1845)Cag>Tag | p.Q615* |
| BLCA | 9 | 131345412 | 131345412 | + | Silent | SNP | C | C | T | TCGA-4Z-AA7W-01A-11D-A391-08 | TCGA-4Z-AA7W-10A-01D-A394-08 | g.chr9:131345412C>T | c.1863C>T | c.(1861-1863)ctC>ctT | p.L621L |
| BLCA | 9 | 131346585 | 131346585 | + | Missense_Mutation | SNP | C | C | G | TCGA-4Z-AA7W-01A-11D-A391-08 | TCGA-4Z-AA7W-10A-01D-A394-08 | g.chr9:131346585C>G | c.2218C>G | c.(2218-2220)Cag>Gag | p.Q740E |
| BLCA | 9 | 131346653 | 131346653 | + | Silent | SNP | C | C | T | TCGA-DK-A1A6-01A-11D-A13W-08 | TCGA-DK-A1A6-10A-01D-A13W-08 | g.chr9:131346653C>T | c.2286C>T | c.(2284-2286)ctC>ctT | p.L762L |
| BLCA | 9 | 131346674 | 131346674 | + | Silent | SNP | C | C | G | TCGA-XF-AAMY-01A-11D-A42E-08 | TCGA-XF-AAMY-10A-01D-A42H-08 | g.chr9:131346674C>G | c.2307C>G | c.(2305-2307)ctC>ctG | p.L769L |
| BLCA | 9 | 131346753 | 131346753 | + | Missense_Mutation | SNP | G | G | C | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chr9:131346753G>C | c.2386G>C | c.(2386-2388)Gag>Cag | p.E796Q |
| BLCA | 9 | 131346760 | 131346760 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A6TK-01A-42D-A339-08 | TCGA-FD-A6TK-10A-21D-A339-08 | g.chr9:131346760C>T | c.2393C>T | c.(2392-2394)aCg>aTg | p.T798M |
| BLCA | 9 | 131346793 | 131346793 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-AAMY-01A-11D-A42E-08 | TCGA-XF-AAMY-10A-01D-A42H-08 | g.chr9:131346793C>G | c.2426C>G | c.(2425-2427)tCt>tGt | p.S809C |
| BLCA | 9 | 131347041 | 131347041 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DK-A1A6-01A-11D-A13W-08 | TCGA-DK-A1A6-10A-01D-A13W-08 | g.chr9:131347041C>T | c.2479C>T | c.(2479-2481)Caa>Taa | p.Q827* |
| BLCA | 9 | 131348062 | 131348062 | + | Missense_Mutation | SNP | C | C | A | TCGA-CF-A47V-01A-11D-A23U-08 | TCGA-CF-A47V-10A-01D-A23U-08 | g.chr9:131348062C>A | c.2596C>A | c.(2596-2598)Cac>Aac | p.H866N |
| BLCA | 9 | 131348070 | 131348070 | + | Silent | SNP | G | G | A | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chr9:131348070G>A | c.2604G>A | c.(2602-2604)ctG>ctA | p.L868L |
| BLCA | 9 | 131348091 | 131348091 | + | Silent | SNP | G | G | A | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chr9:131348091G>A | c.2625G>A | c.(2623-2625)ctG>ctA | p.L875L |
| BLCA | 9 | 131348125 | 131348125 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-FD-A5BZ-01A-11D-A289-08 | TCGA-FD-A5BZ-10A-01D-A289-08 | g.chr9:131348125G>T | c.2659G>T | c.(2659-2661)Gag>Tag | p.E887* |
| BLCA | 9 | 131351141 | 131351141 | + | Silent | SNP | C | C | G | TCGA-DK-AA77-01A-11D-A391-08 | TCGA-DK-AA77-10A-01D-A394-08 | g.chr9:131351141C>G | c.2925C>G | c.(2923-2925)ctC>ctG | p.L975L |
| BLCA | 9 | 131351151 | 131351151 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-BT-A42E-01A-11D-A23U-08 | TCGA-BT-A42E-10A-01D-A23U-08 | g.chr9:131351151C>T | c.2935C>T | c.(2935-2937)Cag>Tag | p.Q979* |
| BLCA | 9 | 131351159 | 131351159 | + | Missense_Mutation | SNP | G | G | C | TCGA-4Z-AA7W-01A-11D-A391-08 | TCGA-4Z-AA7W-10A-01D-A394-08 | g.chr9:131351159G>C | c.2943G>C | c.(2941-2943)aaG>aaC | p.K981N |
| BLCA | 9 | 131355317 | 131355317 | + | Missense_Mutation | SNP | G | G | C | TCGA-CF-A47V-01A-11D-A23U-08 | TCGA-CF-A47V-10A-01D-A23U-08 | g.chr9:131355317G>C | c.3211G>C | c.(3211-3213)Gaa>Caa | p.E1071Q |
| BLCA | 9 | 131356499 | 131356499 | + | Silent | SNP | G | G | A | TCGA-BT-A42C-01A-11D-A23M-08 | TCGA-BT-A42C-10A-01D-A23K-08 | g.chr9:131356499G>A | c.3261G>A | c.(3259-3261)ttG>ttA | p.L1087L |
| BLCA | 9 | 131356505 | 131356505 | + | Missense_Mutation | SNP | G | G | C | TCGA-4Z-AA7W-01A-11D-A391-08 | TCGA-4Z-AA7W-10A-01D-A394-08 | g.chr9:131356505G>C | c.3267G>C | c.(3265-3267)aaG>aaC | p.K1089N |
| BLCA | 9 | 131356542 | 131356542 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-BT-A42C-01A-11D-A23M-08 | TCGA-BT-A42C-10A-01D-A23K-08 | g.chr9:131356542G>T | c.3304G>T | c.(3304-3306)Gaa>Taa | p.E1102* |
| BLCA | 9 | 131356617 | 131356617 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9T8-01A-11D-A391-08 | TCGA-XF-A9T8-10A-01D-A394-08 | g.chr9:131356617G>A | c.3379G>A | c.(3379-3381)Gag>Aag | p.E1127K |
| BLCA | 9 | 131362362 | 131362362 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A42C-01A-11D-A23M-08 | TCGA-BT-A42C-10A-01D-A23K-08 | g.chr9:131362362G>A | c.3547G>A | c.(3547-3549)Gaa>Aaa | p.E1183K |
| BLCA | 9 | 131362391 | 131362391 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DK-A6B5-01A-11D-A31L-08 | TCGA-DK-A6B5-10A-01D-A31J-08 | g.chr9:131362391G>A | c.3576G>A | c.(3574-3576)tgG>tgA | p.W1192* |
| BLCA | 9 | 131367332 | 131367332 | + | Missense_Mutation | SNP | G | G | C | TCGA-BT-A42C-01A-11D-A23M-08 | TCGA-BT-A42C-10A-01D-A23K-08 | g.chr9:131367332G>C | c.3739G>C | c.(3739-3741)Gaa>Caa | p.E1247Q |
| BLCA | 9 | 131367341 | 131367341 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A2I1-01A-11D-A17V-08 | TCGA-DK-A2I1-10A-01D-A17V-08 | g.chr9:131367341G>A | c.3748G>A | c.(3748-3750)Gaa>Aaa | p.E1250K |
| BLCA | 9 | 131367428 | 131367429 | + | Frame_Shift_Del | DEL | GA | GA | - | TCGA-G2-A2EC-01A-11D-A17V-08 | TCGA-G2-A2EC-10A-01D-A17V-08 | g.chr9:131367428_131367429delGA | c.3835_3836delGA | c.(3835-3837)gagfs | p.E1279fs |
| BLCA | 9 | 131369932 | 131369932 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-G2-A2EO-01A-11D-A17V-08 | TCGA-G2-A2EO-11A-21D-A17V-08 | g.chr9:131369932G>T | c.4096G>T | c.(4096-4098)Gag>Tag | p.E1366* |
| BLCA | 9 | 131370143 | 131370143 | + | Missense_Mutation | SNP | G | G | A | TCGA-GU-A766-01A-11D-A32B-08 | TCGA-GU-A766-10A-01D-A329-08 | g.chr9:131370143G>A | c.4159G>A | c.(4159-4161)Gaa>Aaa | p.E1387K |
| BLCA | 9 | 131370245 | 131370245 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131370245G>A | c.4261G>A | c.(4261-4263)Gat>Aat | p.D1421N |
| BLCA | 9 | 131370275 | 131370275 | + | Missense_Mutation | SNP | G | G | C | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131370275G>C | c.4291G>C | c.(4291-4293)Gag>Cag | p.E1431Q |
| BLCA | 9 | 131370487 | 131370487 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131370487G>A | c.4423G>A | c.(4423-4425)Gac>Aac | p.D1475N |
| BLCA | 9 | 131370491 | 131370491 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-UY-A9PH-01A-11D-A38G-08 | TCGA-UY-A9PH-10A-01D-A38J-08 | g.chr9:131370491C>G | c.4427C>G | c.(4426-4428)tCa>tGa | p.S1476* |
| BLCA | 9 | 131371153 | 131371154 | + | Splice_Site | INS | - | - | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131371153_131371154insA | c.4492_4493insA | c.(4492-4494)gaa>gAaa | p.E1498fs |
| BLCA | 9 | 131371219 | 131371219 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131371219G>A | c.4558G>A | c.(4558-4560)Gga>Aga | p.G1520R |
| BLCA | 9 | 131371243 | 131371243 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131371243G>A | c.4582G>A | c.(4582-4584)Gag>Aag | p.E1528K |
| BLCA | 9 | 131371429 | 131371429 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131371429G>A | c.4624G>A | c.(4624-4626)Gag>Aag | p.E1542K |
| BLCA | 9 | 131371450 | 131371450 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-DK-A3WY-01A-11D-A22Z-08 | TCGA-DK-A3WY-10A-01D-A22Z-08 | g.chr9:131371450G>T | c.4645G>T | c.(4645-4647)Gaa>Taa | p.E1549* |
| BLCA | 9 | 131371495 | 131371495 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131371495G>A | c.4690G>A | c.(4690-4692)Gag>Aag | p.E1564K |
| BLCA | 9 | 131374105 | 131374105 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131374105G>A | c.4871G>A | c.(4870-4872)gGc>gAc | p.G1624D |
| BLCA | 9 | 131374110 | 131374110 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131374110G>A | c.4876G>A | c.(4876-4878)Gag>Aag | p.E1626K |
| BLCA | 9 | 131374459 | 131374459 | + | Silent | SNP | G | G | A | TCGA-GU-A766-01A-11D-A32B-08 | TCGA-GU-A766-10A-01D-A329-08 | g.chr9:131374459G>A | c.4962G>A | c.(4960-4962)ctG>ctA | p.L1654L |
| BLCA | 9 | 131374468 | 131374469 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-DK-A1AA-01A-11D-A13W-08 | TCGA-DK-A1AA-10A-01D-A13W-08 | g.chr9:131374468_131374469insT | c.4971_4972insT | c.(4972-4974)aacfs | p.N1658fs |
| BLCA | 9 | 131375659 | 131375659 | + | Splice_Site | SNP | G | G | A | TCGA-ZF-A9RL-01A-11D-A38G-08 | TCGA-ZF-A9RL-10A-01D-A38J-08 | g.chr9:131375659G>A | | c.e39-1 | |
| BLCA | 9 | 131377919 | 131377919 | + | Silent | SNP | G | G | A | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131377919G>A | c.5142G>A | c.(5140-5142)ctG>ctA | p.L1714L |
| BLCA | 9 | 131378024 | 131378024 | + | Silent | SNP | C | C | T | TCGA-GU-A766-01A-11D-A32B-08 | TCGA-GU-A766-10A-01D-A329-08 | g.chr9:131378024C>T | c.5247C>T | c.(5245-5247)atC>atT | p.I1749I |
| BLCA | 9 | 131378027 | 131378027 | + | Missense_Mutation | SNP | G | G | C | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131378027G>C | c.5250G>C | c.(5248-5250)aaG>aaC | p.K1750N |
| BLCA | 9 | 131378038 | 131378038 | + | Missense_Mutation | SNP | C | C | T | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr9:131378038C>T | c.5261C>T | c.(5260-5262)gCc>gTc | p.A1754V |
| BLCA | 9 | 131378100 | 131378100 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A42C-01A-11D-A23M-08 | TCGA-BT-A42C-10A-01D-A23K-08 | g.chr9:131378100G>A | c.5323G>A | c.(5323-5325)Gac>Aac | p.D1775N |
| BLCA | 9 | 131379913 | 131379931 | + | Splice_Site | DEL | ATTCAGGGAGAAGAAGCTG | ATTCAGGGAGAAGAAGCTG | - | TCGA-FD-A6TI-01A-11D-A32B-08 | TCGA-FD-A6TI-10A-01D-A329-08 | g.chr9:131379913_131379931delATTCAGGGAGAAGAAGCTG | c.5342_5355delATTCAGGGAGAAGAAGCTG | c.(5341-5355)aattcagggagaaga>a | p.NSGRR1781fs |
| BLCA | 9 | 131379944 | 131379944 | + | Missense_Mutation | SNP | G | G | C | TCGA-GC-A3BM-01A-11D-A22Z-08 | TCGA-GC-A3BM-10A-01D-A22Z-08 | g.chr9:131379944G>C | c.5368G>C | c.(5368-5370)Gag>Cag | p.E1790Q |
| BLCA | 9 | 131379988 | 131379988 | + | Missense_Mutation | SNP | G | G | T | TCGA-GC-A3BM-01A-11D-A22Z-08 | TCGA-GC-A3BM-10A-01D-A22Z-08 | g.chr9:131379988G>T | c.5412G>T | c.(5410-5412)aaG>aaT | p.K1804N |
| BLCA | 9 | 131380380 | 131380380 | + | Missense_Mutation | SNP | G | G | T | TCGA-GC-A3BM-01A-11D-A22Z-08 | TCGA-GC-A3BM-10A-01D-A22Z-08 | g.chr9:131380380G>T | c.5578G>T | c.(5578-5580)Gct>Tct | p.A1860S |
| BLCA | 9 | 131381181 | 131381181 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-AAN0-01A-11D-A42E-08 | TCGA-XF-AAN0-10A-01D-A42H-08 | g.chr9:131381181C>G | c.5617C>G | c.(5617-5619)Cag>Gag | p.Q1873E |
| BLCA | 9 | 131381207 | 131381207 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-GC-A3BM-01A-11D-A22Z-08 | TCGA-GC-A3BM-10A-01D-A22Z-08 | g.chr9:131381207delG | c.5643delG | c.(5641-5643)gagfs | p.E1883fs |
| BLCA | 9 | 131381222 | 131381222 | + | Silent | SNP | C | C | A | TCGA-GU-A766-01A-11D-A32B-08 | TCGA-GU-A766-10A-01D-A329-08 | g.chr9:131381222C>A | c.5658C>A | c.(5656-5658)atC>atA | p.I1886I |
| BLCA | 9 | 131381226 | 131381226 | + | Missense_Mutation | SNP | G | G | A | TCGA-GC-A3BM-01A-11D-A22Z-08 | TCGA-GC-A3BM-10A-01D-A22Z-08 | g.chr9:131381226G>A | c.5662G>A | c.(5662-5664)Gag>Aag | p.E1888K |
| BLCA | 9 | 131386673 | 131386673 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-CF-A7I0-01A-22D-A34U-08 | TCGA-CF-A7I0-10A-01D-A34X-08 | g.chr9:131386673G>T | c.5884G>T | c.(5884-5886)Gag>Tag | p.E1962* |
| BLCA | 9 | 131386709 | 131386709 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A42F-01A-11D-A23U-08 | TCGA-BT-A42F-10A-01D-A23U-08 | g.chr9:131386709G>A | c.5920G>A | c.(5920-5922)Gag>Aag | p.E1974K |
| BLCA | 9 | 131386709 | 131386709 | + | Missense_Mutation | SNP | G | G | A | TCGA-GV-A6ZA-01A-12D-A339-08 | TCGA-GV-A6ZA-10A-01D-A339-08 | g.chr9:131386709G>A | c.5920G>A | c.(5920-5922)Gag>Aag | p.E1974K |
| BLCA | 9 | 131386754 | 131386754 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-GV-A6ZA-01A-12D-A339-08 | TCGA-GV-A6ZA-10A-01D-A339-08 | g.chr9:131386754G>T | c.5965G>T | c.(5965-5967)Gag>Tag | p.E1989* |
| BLCA | 9 | 131387392 | 131387392 | + | Silent | SNP | G | G | A | TCGA-DK-A3IK-01A-32D-A21A-08 | TCGA-DK-A3IK-10A-01D-A21A-08 | g.chr9:131387392G>A | c.5988G>A | c.(5986-5988)gaG>gaA | p.E1996E |
| BLCA | 9 | 131388155 | 131388155 | + | Silent | SNP | C | C | T | TCGA-BL-A3JM-01A-12D-A21A-08 | TCGA-BL-A3JM-11A-31D-A21A-08 | g.chr9:131388155C>T | c.6162C>T | c.(6160-6162)atC>atT | p.I2054I |
| BLCA | 9 | 131388257 | 131388257 | + | Splice_Site | SNP | G | G | A | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr9:131388257G>A | c.6264G>A | c.(6262-6264)aaG>aaA | p.K2088K |
| BLCA | 9 | 131388682 | 131388682 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-FD-A3SQ-01A-21D-A22Z-08 | TCGA-FD-A3SQ-10A-01D-A22Z-08 | g.chr9:131388682delT | c.6277delT | c.(6277-6279)ttcfs | p.F2093fs |
| BLCA | 9 | 131388736 | 131388736 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A20R-01A-12D-A16O-08 | TCGA-BT-A20R-11A-11D-A16O-08 | g.chr9:131388736G>A | c.6331G>A | c.(6331-6333)Gag>Aag | p.E2111K |
| BLCA | 9 | 131388859 | 131388859 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SR-01A-11D-A22Z-08 | TCGA-FD-A3SR-10A-01D-A22Z-08 | g.chr9:131388859G>A | c.6454G>A | c.(6454-6456)Gag>Aag | p.E2152K |
| BLCA | 9 | 131388960 | 131388960 | + | Silent | SNP | C | C | A | TCGA-CF-A5U8-01A-11D-A289-08 | TCGA-CF-A5U8-10A-01D-A289-08 | g.chr9:131388960C>A | c.6555C>A | c.(6553-6555)atC>atA | p.I2185I |
| BLCA | 9 | 131392643 | 131392643 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SN-01A-12D-A22Z-08 | TCGA-FD-A3SN-10A-01D-A22Z-08 | g.chr9:131392643G>A | c.6736G>A | c.(6736-6738)Gaa>Aaa | p.E2246K |
| BLCA | 9 | 131394415 | 131394415 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-2F-A9KQ-01A-11D-A38G-08 | TCGA-2F-A9KQ-11A-11D-A38J-08 | g.chr9:131394415C>T | c.6757C>T | c.(6757-6759)Cag>Tag | p.Q2253* |
| BLCA | 9 | 131394708 | 131394708 | + | Splice_Site | SNP | A | A | G | TCGA-XF-A9SV-01A-21D-A42E-08 | TCGA-XF-A9SV-10A-01D-A42H-08 | g.chr9:131394708A>G | | c.e53-1 | |
| BLCA | 9 | 131394948 | 131394948 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A42C-01A-11D-A23M-08 | TCGA-BT-A42C-10A-01D-A23K-08 | g.chr9:131394948G>A | c.7096G>A | c.(7096-7098)Gaa>Aaa | p.E2366K |
| BLCA | 9 | 131395126 | 131395126 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A0YX-01A-11D-A10S-08 | TCGA-BT-A0YX-10A-01D-A10S-08 | g.chr9:131395126G>A | c.7185G>A | c.(7183-7185)atG>atA | p.M2395I |
| BLCA | 9 | 131395173 | 131395182 | + | Frame_Shift_Del | DEL | GCGCCTTCCG | GCGCCTTCCG | - | TCGA-FD-A6TB-01A-12D-A339-08 | TCGA-FD-A6TB-10A-21D-A339-08 | g.chr9:131395173_131395182delGCGCCTTCCG | c.7232_7241delGCGCCTTCCG | c.(7231-7242)agcgccttccggfs | p.SAFR2411fs |
| BLCA | 9 | 131395609 | 131395609 | + | Missense_Mutation | SNP | A | A | G | TCGA-XF-AAN1-01A-31D-A42E-08 | TCGA-XF-AAN1-10A-01D-A42H-08 | g.chr9:131395609A>G | c.7415A>G | c.(7414-7416)aAc>aGc | p.N2472S |
| BRCA | 9 | 131346108 | 131346108 | + | Missense_Mutation | SNP | C | C | T | TCGA-A7-A13E-01A-11D-A272-09 | TCGA-A7-A13E-10A-02D-A272-09 | g.chr9:131346108C>T | c.2053C>T | c.(2053-2055)Cgc>Tgc | p.R685C |
| BRCA | 9 | 131346738 | 131346738 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr9:131346738C>T | c.2371C>T | c.(2371-2373)Cgg>Tgg | p.R791W |
| BRCA | 9 | 131347092 | 131347092 | + | Missense_Mutation | SNP | A | A | G | TCGA-E9-A54Y-01A-11D-A25Q-09 | TCGA-E9-A54Y-10A-01D-A25Q-09 | g.chr9:131347092A>G | c.2530A>G | c.(2530-2532)Aca>Gca | p.T844A |
| BRCA | 9 | 131360679 | 131360679 | + | Splice_Site | SNP | G | G | C | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chr9:131360679G>C | c.3415G>C | c.(3415-3417)Gac>Cac | p.D1139H |
| BRCA | 9 | 131367318 | 131367318 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A27M-01A-11D-A16D-09 | TCGA-D8-A27M-10A-01D-A16D-09 | g.chr9:131367318C>G | c.3725C>G | c.(3724-3726)gCt>gGt | p.A1242G |
| BRCA | 9 | 131370243 | 131370243 | + | Missense_Mutation | SNP | T | T | G | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr9:131370243T>G | c.4259T>G | c.(4258-4260)cTt>cGt | p.L1420R |
| BRCA | 9 | 131371190 | 131371190 | + | Missense_Mutation | SNP | A | A | C | TCGA-E9-A1R5-01A-11D-A14K-09 | TCGA-E9-A1R5-10A-01D-A14K-09 | g.chr9:131371190A>C | c.4529A>C | c.(4528-4530)cAg>cCg | p.Q1510P |
| BRCA | 9 | 131371503 | 131371503 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr9:131371503G>C | c.4698G>C | c.(4696-4698)tgG>tgC | p.W1566C |
| BRCA | 9 | 131374449 | 131374450 | + | Missense_Mutation | DNP | GC | GC | AG | TCGA-AR-A254-01A-21D-A167-09 | TCGA-AR-A254-10A-01D-A167-09 | g.chr9:131374449_131374450GC>AG | c.4952_4953GC>AG | c.(4951-4953)aGC>aAG | p.S1651K |
| BRCA | 9 | 131378115 | 131378115 | + | Missense_Mutation | SNP | A | A | G | TCGA-BH-A0BW-01A-11D-A10Y-09 | TCGA-BH-A0BW-10A-01D-A110-09 | g.chr9:131378115A>G | c.5338A>G | c.(5338-5340)Atc>Gtc | p.I1780V |
| BRCA | 9 | 131380311 | 131380311 | + | Missense_Mutation | SNP | G | G | A | TCGA-A2-A0T1-01A-21D-A099-09 | TCGA-A2-A0T1-10A-01D-A099-09 | g.chr9:131380311G>A | c.5509G>A | c.(5509-5511)Ggg>Agg | p.G1837R |
| BRCA | 9 | 131394575 | 131394575 | + | Missense_Mutation | SNP | A | A | G | TCGA-A2-A3XY-01A-11D-A23C-09 | TCGA-A2-A3XY-10A-01D-A23C-09 | g.chr9:131394575A>G | c.6917A>G | c.(6916-6918)cAc>cGc | p.H2306R |
| CESC | 9 | 131331147 | 131331147 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A1BI-01B-11D-A13W-08 | TCGA-C5-A1BI-10A-01D-A13W-08 | g.chr9:131331147G>A | c.334G>A | c.(334-336)Gaa>Aaa | p.E112K |
| CESC | 9 | 131344825 | 131344825 | + | Missense_Mutation | SNP | G | G | A | TCGA-DS-A0VN-01A-21D-A10S-08 | TCGA-DS-A0VN-10A-01D-A10S-08 | g.chr9:131344825G>A | c.1640G>A | c.(1639-1641)cGc>cAc | p.R547H |
| CESC | 9 | 131345069 | 131345069 | + | Missense_Mutation | SNP | G | G | C | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr9:131345069G>C | c.1747G>C | c.(1747-1749)Gat>Cat | p.D583H |
| CESC | 9 | 131345416 | 131345416 | + | Missense_Mutation | SNP | G | G | A | TCGA-Q1-A73Q-01A-21D-A32I-09 | TCGA-Q1-A73Q-10B-01D-A32I-09 | g.chr9:131345416G>A | c.1867G>A | c.(1867-1869)Gca>Aca | p.A623T |
| CESC | 9 | 131346188 | 131346188 | + | Silent | SNP | C | C | G | TCGA-EK-A2RC-01A-11D-A18J-09 | TCGA-EK-A2RC-10A-01D-A18J-09 | g.chr9:131346188C>G | c.2133C>G | c.(2131-2133)acC>acG | p.T711T |
| CESC | 9 | 131346737 | 131346737 | + | Silent | SNP | C | C | T | TCGA-MY-A5BD-01A-11D-A26G-09 | TCGA-MY-A5BD-10A-01D-A26G-09 | g.chr9:131346737C>T | c.2370C>T | c.(2368-2370)ttC>ttT | p.F790F |
| CESC | 9 | 131348188 | 131348188 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-MY-A5BD-01A-11D-A26G-09 | TCGA-MY-A5BD-10A-01D-A26G-09 | g.chr9:131348188G>T | c.2722G>T | c.(2722-2724)Gag>Tag | p.E908* |
| CESC | 9 | 131351132 | 131351132 | + | Silent | SNP | C | C | G | TCGA-FU-A23K-01A-11D-A16O-08 | TCGA-FU-A23K-10A-01D-A16O-08 | g.chr9:131351132C>G | c.2916C>G | c.(2914-2916)gtC>gtG | p.V972V |
| CESC | 9 | 131356479 | 131356479 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr9:131356479G>A | c.3241G>A | c.(3241-3243)Gag>Aag | p.E1081K |
| CESC | 9 | 131362362 | 131362362 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-EK-A2RJ-01A-11D-A18J-09 | TCGA-EK-A2RJ-10A-01D-A18J-09 | g.chr9:131362362delG | c.3547delG | c.(3547-3549)gaafs | p.E1183fs |
| CESC | 9 | 131386727 | 131386727 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FU-A5XV-01A-11D-A28B-09 | TCGA-FU-A5XV-10A-01D-A28E-09 | g.chr9:131386727C>T | c.5938C>T | c.(5938-5940)Cag>Tag | p.Q1980* |
| CESC | 9 | 131386727 | 131386727 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-MU-A51Y-01A-11D-A26G-09 | TCGA-MU-A51Y-10A-01D-A26G-09 | g.chr9:131386727C>T | c.5938C>T | c.(5938-5940)Cag>Tag | p.Q1980* |
| CESC | 9 | 131389689 | 131389689 | + | Missense_Mutation | SNP | G | G | A | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr9:131389689G>A | c.6586G>A | c.(6586-6588)Gaa>Aaa | p.E2196K |
| CESC | 9 | 131395165 | 131395165 | + | Silent | SNP | G | G | A | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr9:131395165G>A | c.7224G>A | c.(7222-7224)gaG>gaA | p.E2408E |
| CESC | 9 | 131395181 | 131395181 | + | Missense_Mutation | SNP | C | C | T | TCGA-MU-A5YI-01A-11D-A32I-09 | TCGA-MU-A5YI-10A-01D-A32I-09 | g.chr9:131395181C>T | c.7240C>T | c.(7240-7242)Cgg>Tgg | p.R2414W |
| CHOL | 9 | 131348107 | 131348107 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-3X-AAVE-01A-11D-A417-09 | TCGA-3X-AAVE-10A-01D-A41A-09 | g.chr9:131348107C>T | c.2641C>T | c.(2641-2643)Cag>Tag | p.Q881* |
| COAD | 9 | 131344063 | 131344063 | + | Silent | SNP | G | G | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr9:131344063G>A | c.1464G>A | c.(1462-1464)gcG>gcA | p.A488A |
| COAD | 9 | 131344156 | 131344156 | + | Silent | SNP | G | G | A | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr9:131344156G>A | c.1557G>A | c.(1555-1557)caG>caA | p.Q519Q |
| COAD | 9 | 131344999 | 131344999 | + | Silent | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr9:131344999C>T | c.1677C>T | c.(1675-1677)caC>caT | p.H559H |
| COAD | 9 | 131345102 | 131345102 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr9:131345102delA | c.1780delA | c.(1780-1782)aaafs | p.K594fs |
| COAD | 9 | 131345476 | 131345476 | + | Missense_Mutation | SNP | C | C | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr9:131345476C>A | c.1927C>A | c.(1927-1929)Cac>Aac | p.H643N |
| COAD | 9 | 131346136 | 131346136 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr9:131346136T>C | c.2081T>C | c.(2080-2082)cTa>cCa | p.L694P |
| COAD | 9 | 131346164 | 131346164 | + | Silent | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr9:131346164G>A | c.2109G>A | c.(2107-2109)tcG>tcA | p.S703S |
| COAD | 9 | 131346595 | 131346595 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr9:131346595A>C | c.2228A>C | c.(2227-2229)cAg>cCg | p.Q743P |
| COAD | 9 | 131346768 | 131346768 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr9:131346768C>T | c.2401C>T | c.(2401-2403)Cga>Tga | p.R801* |
| COAD | 9 | 131348167 | 131348167 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr9:131348167G>A | c.2701G>A | c.(2701-2703)Gag>Aag | p.E901K |
| COAD | 9 | 131348235 | 131348236 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr9:131348235_131348236delCT | c.2769_2770delCT | c.(2767-2772)gactctfs | p.S924fs |
| COAD | 9 | 131351167 | 131351167 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr9:131351167G>A | c.2951G>A | c.(2950-2952)cGa>cAa | p.R984Q |
| COAD | 9 | 131353800 | 131353800 | + | Silent | SNP | G | G | A | TCGA-AY-6386-01A-21D-1719-10 | TCGA-AY-6386-10A-01D-1719-10 | g.chr9:131353800G>A | c.3051G>A | c.(3049-3051)ccG>ccA | p.P1017P |
| COAD | 9 | 131353800 | 131353800 | + | Silent | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr9:131353800G>A | c.3051G>A | c.(3049-3051)ccG>ccA | p.P1017P |
| COAD | 9 | 131353800 | 131353800 | + | Silent | SNP | G | G | A | TCGA-G4-6315-01A-11D-1719-10 | TCGA-G4-6315-10A-01D-1720-10 | g.chr9:131353800G>A | c.3051G>A | c.(3049-3051)ccG>ccA | p.P1017P |
| COAD | 9 | 131353809 | 131353809 | + | Silent | SNP | C | C | T | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr9:131353809C>T | c.3060C>T | c.(3058-3060)taC>taT | p.Y1020Y |
| COAD | 9 | 131353828 | 131353828 | + | Missense_Mutation | SNP | G | G | A | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr9:131353828G>A | c.3079G>A | c.(3079-3081)Gcc>Acc | p.A1027T |
| COAD | 9 | 131360733 | 131360733 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr9:131360733C>A | c.3469C>A | c.(3469-3471)Ctg>Atg | p.L1157M |
| COAD | 9 | 131360734 | 131360734 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6161-01A-11D-1650-10 | TCGA-CM-6161-10A-01D-1650-10 | g.chr9:131360734T>C | c.3470T>C | c.(3469-3471)cTg>cCg | p.L1157P |
| COAD | 9 | 131367424 | 131367424 | + | Silent | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr9:131367424C>T | c.3831C>T | c.(3829-3831)ggC>ggT | p.G1277G |
| COAD | 9 | 131367448 | 131367448 | + | Silent | SNP | C | C | T | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr9:131367448C>T | c.3855C>T | c.(3853-3855)ctC>ctT | p.L1285L |
| COAD | 9 | 131367602 | 131367602 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr9:131367602C>T | c.3892C>T | c.(3892-3894)Cgc>Tgc | p.R1298C |
| COAD | 9 | 131369974 | 131369974 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr9:131369974C>T | c.4138C>T | c.(4138-4140)Cga>Tga | p.R1380* |
| COAD | 9 | 131370209 | 131370209 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chr9:131370209G>A | c.4225G>A | c.(4225-4227)Gga>Aga | p.G1409R |
| COAD | 9 | 131370475 | 131370475 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr9:131370475G>A | c.4411G>A | c.(4411-4413)Gaa>Aaa | p.E1471K |
| COAD | 9 | 131371928 | 131371928 | + | Intron | SNP | A | A | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr9:131371928A>G | | | |
| COAD | 9 | 131374040 | 131374040 | + | Silent | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr9:131374040C>T | c.4806C>T | c.(4804-4806)aaC>aaT | p.N1602N |
| COAD | 9 | 131379957 | 131379957 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr9:131379957G>T | c.5381G>T | c.(5380-5382)cGg>cTg | p.R1794L |
| COAD | 9 | 131379981 | 131379981 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr9:131379981T>C | c.5405T>C | c.(5404-5406)cTg>cCg | p.L1802P |
| COAD | 9 | 131380387 | 131380387 | + | Splice_Site | SNP | G | G | A | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr9:131380387G>A | c.5585G>A | c.(5584-5586)cGg>cAg | p.R1862Q |
| COAD | 9 | 131383493 | 131383493 | + | Silent | SNP | C | C | T | TCGA-AA-3851-01A-01W-0995-10 | TCGA-AA-3851-10A-01W-0995-10 | g.chr9:131383493C>T | c.5775C>T | c.(5773-5775)cgC>cgT | p.R1925R |
| COAD | 9 | 131388112 | 131388112 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr9:131388112A>G | c.6119A>G | c.(6118-6120)aAa>aGa | p.K2040R |
| COAD | 9 | 131388738 | 131388738 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr9:131388738G>T | c.6333G>T | c.(6331-6333)gaG>gaT | p.E2111D |
| COAD | 9 | 131388794 | 131388794 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr9:131388794G>A | c.6389G>A | c.(6388-6390)cGc>cAc | p.R2130H |
| COAD | 9 | 131389748 | 131389748 | + | Silent | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr9:131389748C>T | c.6645C>T | c.(6643-6645)aaC>aaT | p.N2215N |
| COAD | 9 | 131394744 | 131394744 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr9:131394744G>T | c.6979G>T | c.(6979-6981)Gaa>Taa | p.E2327* |
| COAD | 9 | 131394910 | 131394910 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr9:131394910G>A | c.7058G>A | c.(7057-7059)cGc>cAc | p.R2353H |
| COAD | 9 | 131394992 | 131394992 | + | Silent | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr9:131394992G>A | c.7140G>A | c.(7138-7140)ccG>ccA | p.P2380P |
| COAD | 9 | 131395091 | 131395091 | + | Missense_Mutation | SNP | G | G | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr9:131395091G>T | c.7150G>T | c.(7150-7152)Ggc>Tgc | p.G2384C |
| COAD | 9 | 131395517 | 131395517 | + | Missense_Mutation | SNP | C | C | G | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr9:131395517C>G | c.7323C>G | c.(7321-7323)tgC>tgG | p.C2441W |
| COAD | 9 | 131395553 | 131395553 | + | Silent | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr9:131395553C>T | c.7359C>T | c.(7357-7359)ggC>ggT | p.G2453G |
| COADREAD | 9 | 131329190 | 131329190 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:131329190G>T | c.171G>T | c.(169-171)gaG>gaT | p.E57D |
| COADREAD | 9 | 131344063 | 131344063 | + | Silent | SNP | G | G | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr9:131344063G>A | c.1464G>A | c.(1462-1464)gcG>gcA | p.A488A |
| COADREAD | 9 | 131344156 | 131344156 | + | Silent | SNP | G | G | A | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr9:131344156G>A | c.1557G>A | c.(1555-1557)caG>caA | p.Q519Q |
| COADREAD | 9 | 131344999 | 131344999 | + | Silent | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr9:131344999C>T | c.1677C>T | c.(1675-1677)caC>caT | p.H559H |
| COADREAD | 9 | 131345102 | 131345102 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr9:131345102delA | c.1780delA | c.(1780-1782)aaafs | p.K594fs |
| COADREAD | 9 | 131345476 | 131345476 | + | Missense_Mutation | SNP | C | C | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr9:131345476C>A | c.1927C>A | c.(1927-1929)Cac>Aac | p.H643N |
| COADREAD | 9 | 131346136 | 131346136 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr9:131346136T>C | c.2081T>C | c.(2080-2082)cTa>cCa | p.L694P |
| COADREAD | 9 | 131346164 | 131346164 | + | Silent | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr9:131346164G>A | c.2109G>A | c.(2107-2109)tcG>tcA | p.S703S |
| COADREAD | 9 | 131346595 | 131346595 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr9:131346595A>C | c.2228A>C | c.(2227-2229)cAg>cCg | p.Q743P |
| COADREAD | 9 | 131346721 | 131346721 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3587-01A-01W-0831-10 | TCGA-AG-3587-10A-01W-0831-10 | g.chr9:131346721G>A | c.2354G>A | c.(2353-2355)cGg>cAg | p.R785Q |
| COADREAD | 9 | 131346768 | 131346768 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr9:131346768C>T | c.2401C>T | c.(2401-2403)Cga>Tga | p.R801* |
| COADREAD | 9 | 131348167 | 131348167 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr9:131348167G>A | c.2701G>A | c.(2701-2703)Gag>Aag | p.E901K |
| COADREAD | 9 | 131348235 | 131348236 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr9:131348235_131348236delCT | c.2769_2770delCT | c.(2767-2772)gactctfs | p.S924fs |
| COADREAD | 9 | 131351167 | 131351167 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr9:131351167G>A | c.2951G>A | c.(2950-2952)cGa>cAa | p.R984Q |
| COADREAD | 9 | 131353800 | 131353800 | + | Silent | SNP | G | G | A | TCGA-AY-6386-01A-21D-1719-10 | TCGA-AY-6386-10A-01D-1719-10 | g.chr9:131353800G>A | c.3051G>A | c.(3049-3051)ccG>ccA | p.P1017P |
| COADREAD | 9 | 131353800 | 131353800 | + | Silent | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr9:131353800G>A | c.3051G>A | c.(3049-3051)ccG>ccA | p.P1017P |
| COADREAD | 9 | 131353800 | 131353800 | + | Silent | SNP | G | G | A | TCGA-DY-A1H8-01A-21D-A152-10 | TCGA-DY-A1H8-10A-01D-A152-10 | g.chr9:131353800G>A | c.3051G>A | c.(3049-3051)ccG>ccA | p.P1017P |
| COADREAD | 9 | 131353800 | 131353800 | + | Silent | SNP | G | G | A | TCGA-G4-6315-01A-11D-1719-10 | TCGA-G4-6315-10A-01D-1720-10 | g.chr9:131353800G>A | c.3051G>A | c.(3049-3051)ccG>ccA | p.P1017P |
| COADREAD | 9 | 131353809 | 131353809 | + | Silent | SNP | C | C | T | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr9:131353809C>T | c.3060C>T | c.(3058-3060)taC>taT | p.Y1020Y |
| COADREAD | 9 | 131353828 | 131353828 | + | Missense_Mutation | SNP | G | G | A | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr9:131353828G>A | c.3079G>A | c.(3079-3081)Gcc>Acc | p.A1027T |
| COADREAD | 9 | 131360733 | 131360733 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr9:131360733C>A | c.3469C>A | c.(3469-3471)Ctg>Atg | p.L1157M |
| COADREAD | 9 | 131360734 | 131360734 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6161-01A-11D-1650-10 | TCGA-CM-6161-10A-01D-1650-10 | g.chr9:131360734T>C | c.3470T>C | c.(3469-3471)cTg>cCg | p.L1157P |
| COADREAD | 9 | 131367424 | 131367424 | + | Silent | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr9:131367424C>T | c.3831C>T | c.(3829-3831)ggC>ggT | p.G1277G |
| COADREAD | 9 | 131367448 | 131367448 | + | Silent | SNP | C | C | T | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr9:131367448C>T | c.3855C>T | c.(3853-3855)ctC>ctT | p.L1285L |
| COADREAD | 9 | 131367602 | 131367602 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr9:131367602C>T | c.3892C>T | c.(3892-3894)Cgc>Tgc | p.R1298C |
| COADREAD | 9 | 131369974 | 131369974 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr9:131369974C>T | c.4138C>T | c.(4138-4140)Cga>Tga | p.R1380* |
| COADREAD | 9 | 131370209 | 131370209 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chr9:131370209G>A | c.4225G>A | c.(4225-4227)Gga>Aga | p.G1409R |
| COADREAD | 9 | 131370209 | 131370209 | + | Missense_Mutation | SNP | G | G | A | TCGA-DY-A1DC-01A-31D-A152-10 | TCGA-DY-A1DC-10A-01D-A152-10 | g.chr9:131370209G>A | c.4225G>A | c.(4225-4227)Gga>Aga | p.G1409R |
| COADREAD | 9 | 131370475 | 131370475 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr9:131370475G>A | c.4411G>A | c.(4411-4413)Gaa>Aaa | p.E1471K |
| COADREAD | 9 | 131371928 | 131371928 | + | Intron | SNP | A | A | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr9:131371928A>G | | | |
| COADREAD | 9 | 131374040 | 131374040 | + | Silent | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr9:131374040C>T | c.4806C>T | c.(4804-4806)aaC>aaT | p.N1602N |
| COADREAD | 9 | 131374463 | 131374463 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:131374463G>T | c.4966G>T | c.(4966-4968)Gaa>Taa | p.E1656* |
| COADREAD | 9 | 131379957 | 131379957 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr9:131379957G>T | c.5381G>T | c.(5380-5382)cGg>cTg | p.R1794L |
| COADREAD | 9 | 131379971 | 131379971 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:131379971G>A | c.5395G>A | c.(5395-5397)Gtg>Atg | p.V1799M |
| COADREAD | 9 | 131379981 | 131379981 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr9:131379981T>C | c.5405T>C | c.(5404-5406)cTg>cCg | p.L1802P |
| COADREAD | 9 | 131380387 | 131380387 | + | Splice_Site | SNP | G | G | A | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr9:131380387G>A | c.5585G>A | c.(5584-5586)cGg>cAg | p.R1862Q |
| COADREAD | 9 | 131383493 | 131383493 | + | Silent | SNP | C | C | T | TCGA-AA-3851-01A-01W-0995-10 | TCGA-AA-3851-10A-01W-0995-10 | g.chr9:131383493C>T | c.5775C>T | c.(5773-5775)cgC>cgT | p.R1925R |
| COADREAD | 9 | 131388112 | 131388112 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr9:131388112A>G | c.6119A>G | c.(6118-6120)aAa>aGa | p.K2040R |
| COADREAD | 9 | 131388738 | 131388738 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr9:131388738G>T | c.6333G>T | c.(6331-6333)gaG>gaT | p.E2111D |
| COADREAD | 9 | 131388794 | 131388794 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr9:131388794G>A | c.6389G>A | c.(6388-6390)cGc>cAc | p.R2130H |
| COADREAD | 9 | 131389742 | 131389742 | + | Silent | SNP | C | C | T | TCGA-DY-A1DG-01A-11D-A152-10 | TCGA-DY-A1DG-10A-01D-A152-10 | g.chr9:131389742C>T | c.6639C>T | c.(6637-6639)caC>caT | p.H2213H |
| COADREAD | 9 | 131389748 | 131389748 | + | Silent | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr9:131389748C>T | c.6645C>T | c.(6643-6645)aaC>aaT | p.N2215N |
| COADREAD | 9 | 131394744 | 131394744 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr9:131394744G>T | c.6979G>T | c.(6979-6981)Gaa>Taa | p.E2327* |
| COADREAD | 9 | 131394910 | 131394910 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr9:131394910G>A | c.7058G>A | c.(7057-7059)cGc>cAc | p.R2353H |
| COADREAD | 9 | 131394992 | 131394992 | + | Silent | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr9:131394992G>A | c.7140G>A | c.(7138-7140)ccG>ccA | p.P2380P |
| COADREAD | 9 | 131395091 | 131395091 | + | Missense_Mutation | SNP | G | G | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr9:131395091G>T | c.7150G>T | c.(7150-7152)Ggc>Tgc | p.G2384C |
| COADREAD | 9 | 131395517 | 131395517 | + | Missense_Mutation | SNP | C | C | G | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr9:131395517C>G | c.7323C>G | c.(7321-7323)tgC>tgG | p.C2441W |
| COADREAD | 9 | 131395553 | 131395553 | + | Silent | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr9:131395553C>T | c.7359C>T | c.(7357-7359)ggC>ggT | p.G2453G |
| DLBC | 9 | 131362361 | 131362361 | + | Silent | SNP | T | T | C | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr9:131362361T>C | c.3546T>C | c.(3544-3546)gaT>gaC | p.D1182D |
| DLBC | 9 | 131371241 | 131371241 | + | Missense_Mutation | SNP | A | A | G | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr9:131371241A>G | c.4580A>G | c.(4579-4581)aAt>aGt | p.N1527S |
| DLBC | 9 | 131395568 | 131395568 | + | Silent | SNP | C | C | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr9:131395568C>T | c.7374C>T | c.(7372-7374)acC>acT | p.T2458T |
| ESCA | 9 | 131337616 | 131337616 | + | Missense_Mutation | SNP | C | C | G | TCGA-L5-A4OS-01A-11D-A28B-09 | TCGA-L5-A4OS-11A-11D-A28E-09 | g.chr9:131337616C>G | c.643C>G | c.(643-645)Ctc>Gtc | p.L215V |
| ESCA | 9 | 131339485 | 131339485 | + | Missense_Mutation | SNP | C | C | G | TCGA-L5-A891-01A-11D-A36J-09 | TCGA-L5-A891-11A-21D-A36M-09 | g.chr9:131339485C>G | c.863C>G | c.(862-864)gCa>gGa | p.A288G |
| ESCA | 9 | 131344063 | 131344063 | + | Silent | SNP | G | G | A | TCGA-R6-A6KZ-01A-11D-A31U-09 | TCGA-R6-A6KZ-10A-01D-A31U-09 | g.chr9:131344063G>A | c.1464G>A | c.(1462-1464)gcG>gcA | p.A488A |
| ESCA | 9 | 131345085 | 131345085 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A8NQ-01A-11D-A36J-09 | TCGA-L5-A8NQ-11A-11D-A36M-09 | g.chr9:131345085G>T | c.1763G>T | c.(1762-1764)tGg>tTg | p.W588L |
| ESCA | 9 | 131353868 | 131353868 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A8NI-01A-11D-A37C-09 | TCGA-L5-A8NI-11A-11D-A37F-09 | g.chr9:131353868G>A | c.3119G>A | c.(3118-3120)gGc>gAc | p.G1040D |
| ESCA | 9 | 131370264 | 131370264 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-IG-A3YB-01A-11D-A247-09 | TCGA-IG-A3YB-10A-01D-A247-09 | g.chr9:131370264delG | c.4280delG | c.(4279-4281)cgtfs | p.R1427fs |
| ESCA | 9 | 131370475 | 131370475 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-L5-A8NH-01A-11D-A37C-09 | TCGA-L5-A8NH-11A-11D-A37F-09 | g.chr9:131370475G>T | c.4411G>T | c.(4411-4413)Gaa>Taa | p.E1471* |
| ESCA | 9 | 131371514 | 131371514 | + | Missense_Mutation | SNP | A | A | T | TCGA-2H-A9GO-01A-11D-A37C-09 | TCGA-2H-A9GO-11A-11D-A37F-09 | g.chr9:131371514A>T | c.4709A>T | c.(4708-4710)aAa>aTa | p.K1570I |
| ESCA | 9 | 131371527 | 131371527 | + | Silent | SNP | G | G | A | TCGA-Z6-AAPN-01A-11D-A403-09 | TCGA-Z6-AAPN-10A-01D-A403-09 | g.chr9:131371527G>A | c.4722G>A | c.(4720-4722)gcG>gcA | p.A1574A |
| ESCA | 9 | 131388230 | 131388230 | + | Silent | SNP | T | T | G | TCGA-IG-A97I-01A-11D-A387-09 | TCGA-IG-A97I-10A-01D-A38A-09 | g.chr9:131388230T>G | c.6237T>G | c.(6235-6237)ctT>ctG | p.L2079L |
| ESCA | 9 | 131388793 | 131388793 | + | Missense_Mutation | SNP | C | C | T | TCGA-JY-A938-01A-11D-A37C-09 | TCGA-JY-A938-10A-01D-A37F-09 | g.chr9:131388793C>T | c.6388C>T | c.(6388-6390)Cgc>Tgc | p.R2130C |
| ESCA | 9 | 131394492 | 131394492 | + | Silent | SNP | G | G | T | TCGA-IG-A7DP-01A-31D-A33E-09 | TCGA-IG-A7DP-10A-01D-A33H-09 | g.chr9:131394492G>T | c.6834G>T | c.(6832-6834)ctG>ctT | p.L2278L |
| GBM | 9 | 131371470 | 131371470 | + | Missense_Mutation | SNP | G | G | C | TCGA-19-2623-01A-01D-1495-08 | TCGA-19-2623-10A-01D-1495-08 | g.chr9:131371470G>C | c.4665G>C | c.(4663-4665)caG>caC | p.Q1555H |
| GBM | 9 | 131381157 | 131381157 | + | Missense_Mutation | SNP | C | C | T | TCGA-76-6280-01A-21D-1845-08 | TCGA-76-6280-10A-01D-1845-08 | g.chr9:131381157C>T | c.5593C>T | c.(5593-5595)Cgg>Tgg | p.R1865W |
| GBM | 9 | 131395212 | 131395212 | + | Missense_Mutation | SNP | T | T | A | TCGA-06-0158-01A-01D-1491-08 | TCGA-06-0158-10A-01D-1491-08 | g.chr9:131395212T>A | c.7271T>A | c.(7270-7272)gTg>gAg | p.V2424E |
| GBMLGG | 9 | 131337005 | 131337005 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DH-5142-01A-01D-1468-08 | TCGA-DH-5142-10A-01D-1468-08 | g.chr9:131337005C>T | c.415C>T | c.(415-417)Cga>Tga | p.R139* |
| GBMLGG | 9 | 131353798 | 131353798 | + | Missense_Mutation | SNP | C | C | T | TCGA-S9-A7R3-01A-11D-A34J-08 | TCGA-S9-A7R3-10A-01D-A34M-08 | g.chr9:131353798C>T | c.3049C>T | c.(3049-3051)Ccg>Tcg | p.P1017S |
| GBMLGG | 9 | 131371422 | 131371422 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:131371422G>T | c.4617G>T | c.(4615-4617)caG>caT | p.Q1539H |
| GBMLGG | 9 | 131371470 | 131371470 | + | Missense_Mutation | SNP | G | G | C | TCGA-19-2623-01A-01D-1495-08 | TCGA-19-2623-10A-01D-1495-08 | g.chr9:131371470G>C | c.4665G>C | c.(4663-4665)caG>caC | p.Q1555H |
| GBMLGG | 9 | 131381157 | 131381157 | + | Missense_Mutation | SNP | C | C | T | TCGA-76-6280-01A-21D-1845-08 | TCGA-76-6280-10A-01D-1845-08 | g.chr9:131381157C>T | c.5593C>T | c.(5593-5595)Cgg>Tgg | p.R1865W |
| GBMLGG | 9 | 131388217 | 131388217 | + | Missense_Mutation | SNP | G | G | A | TCGA-HT-7875-01A-11D-2395-08 | TCGA-HT-7875-10A-01D-2396-08 | g.chr9:131388217G>A | c.6224G>A | c.(6223-6225)cGc>cAc | p.R2075H |
| GBMLGG | 9 | 131388869 | 131388869 | + | Missense_Mutation | SNP | G | G | A | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr9:131388869G>A | c.6464G>A | c.(6463-6465)cGc>cAc | p.R2155H |
| GBMLGG | 9 | 131395212 | 131395212 | + | Missense_Mutation | SNP | T | T | A | TCGA-06-0158-01A-01D-1491-08 | TCGA-06-0158-10A-01D-1491-08 | g.chr9:131395212T>A | c.7271T>A | c.(7270-7272)gTg>gAg | p.V2424E |
| HNSC | 9 | 131331097 | 131331097 | + | Missense_Mutation | SNP | A | A | T | TCGA-CR-7370-01A-11D-2129-08 | TCGA-CR-7370-10A-01D-2129-08 | g.chr9:131331097A>T | c.284A>T | c.(283-285)aAc>aTc | p.N95I |
| HNSC | 9 | 131339216 | 131339216 | + | Missense_Mutation | SNP | G | G | A | TCGA-UF-A7JT-01A-11D-A34J-08 | TCGA-UF-A7JT-10A-01D-A34M-08 | g.chr9:131339216G>A | c.766G>A | c.(766-768)Gaa>Aaa | p.E256K |
| HNSC | 9 | 131339447 | 131339447 | + | Silent | SNP | G | G | A | TCGA-P3-A6T5-01A-11D-A34J-08 | TCGA-P3-A6T5-10A-01D-A34M-08 | g.chr9:131339447G>A | c.825G>A | c.(823-825)gaG>gaA | p.E275E |
| HNSC | 9 | 131339461 | 131339461 | + | Missense_Mutation | SNP | C | C | G | TCGA-IQ-A61I-01A-11D-A30E-08 | TCGA-IQ-A61I-10A-01D-A30H-08 | g.chr9:131339461C>G | c.839C>G | c.(838-840)tCt>tGt | p.S280C |
| HNSC | 9 | 131339527 | 131339527 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A6JM-01A-11D-A31L-08 | TCGA-CV-A6JM-10A-01D-A31J-08 | g.chr9:131339527G>A | c.905G>A | c.(904-906)aGa>aAa | p.R302K |
| HNSC | 9 | 131339679 | 131339679 | + | Silent | SNP | C | C | T | TCGA-IQ-A61I-01A-11D-A30E-08 | TCGA-IQ-A61I-10A-01D-A30H-08 | g.chr9:131339679C>T | c.979C>T | c.(979-981)Ctg>Ttg | p.L327L |
| HNSC | 9 | 131339775 | 131339775 | + | Missense_Mutation | SNP | G | G | A | TCGA-TN-A7HL-01A-11D-A34J-08 | TCGA-TN-A7HL-10A-01D-A34M-08 | g.chr9:131339775G>A | c.1075G>A | c.(1075-1077)Gat>Aat | p.D359N |
| HNSC | 9 | 131343203 | 131343203 | + | Silent | SNP | G | G | T | TCGA-CV-A6JU-01A-11D-A31L-08 | TCGA-CV-A6JU-10A-01D-A31J-08 | g.chr9:131343203G>T | c.1326G>T | c.(1324-1326)ctG>ctT | p.L442L |
| HNSC | 9 | 131345356 | 131345356 | + | Splice_Site | SNP | G | G | T | TCGA-CV-7411-01A-11D-2078-08 | TCGA-CV-7411-10A-01D-2078-08 | g.chr9:131345356G>T | c.1807G>T | c.(1807-1809)Gat>Tat | p.D603Y |
| HNSC | 9 | 131346592 | 131346592 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-4725-01A-01D-1434-08 | TCGA-CN-4725-10A-01D-1434-08 | g.chr9:131346592G>A | c.2225G>A | c.(2224-2226)cGc>cAc | p.R742H |
| HNSC | 9 | 131348114 | 131348114 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-5326-01A-01D-1870-08 | TCGA-CQ-5326-10A-01D-1870-08 | g.chr9:131348114G>A | c.2648G>A | c.(2647-2649)cGg>cAg | p.R883Q |
| HNSC | 9 | 131348158 | 131348158 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-A6V1-01A-12D-A34J-08 | TCGA-CN-A6V1-10B-01D-A34M-08 | g.chr9:131348158G>A | c.2692G>A | c.(2692-2694)Gat>Aat | p.D898N |
| HNSC | 9 | 131348167 | 131348167 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-6938-01A-11D-1912-08 | TCGA-CV-6938-10A-01D-1912-08 | g.chr9:131348167G>A | c.2701G>A | c.(2701-2703)Gag>Aag | p.E901K |
| HNSC | 9 | 131348215 | 131348215 | + | Missense_Mutation | SNP | G | G | A | TCGA-MZ-A7D7-01A-21D-A34J-08 | TCGA-MZ-A7D7-10A-01D-A34M-08 | g.chr9:131348215G>A | c.2749G>A | c.(2749-2751)Gac>Aac | p.D917N |
| HNSC | 9 | 131351145 | 131351145 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-A63U-01A-11D-A30E-08 | TCGA-CN-A63U-10A-01D-A30H-08 | g.chr9:131351145G>T | c.2929G>T | c.(2929-2931)Gac>Tac | p.D977Y |
| HNSC | 9 | 131362396 | 131362396 | + | Splice_Site | SNP | T | T | G | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr9:131362396T>G | | c.e27+2 | |
| HNSC | 9 | 131367378 | 131367378 | + | Missense_Mutation | SNP | G | G | C | TCGA-CR-7379-01A-11D-2012-08 | TCGA-CR-7379-10A-01D-2013-08 | g.chr9:131367378G>C | c.3785G>C | c.(3784-3786)gGa>gCa | p.G1262A |
| HNSC | 9 | 131370227 | 131370227 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-4741-01A-01D-1434-08 | TCGA-CN-4741-10A-01D-1434-08 | g.chr9:131370227G>A | c.4243G>A | c.(4243-4245)Gag>Aag | p.E1415K |
| HNSC | 9 | 131371248 | 131371248 | + | Silent | SNP | C | C | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr9:131371248C>T | c.4587C>T | c.(4585-4587)gtC>gtT | p.V1529V |
| HNSC | 9 | 131388129 | 131388129 | + | Missense_Mutation | SNP | G | G | A | TCGA-BA-5153-01A-01D-1434-08 | TCGA-BA-5153-10A-01D-1434-08 | g.chr9:131388129G>A | c.6136G>A | c.(6136-6138)Gcc>Acc | p.A2046T |
| HNSC | 9 | 131388253 | 131388253 | + | Missense_Mutation | SNP | G | G | T | TCGA-UF-A7JT-01A-11D-A34J-08 | TCGA-UF-A7JT-10A-01D-A34M-08 | g.chr9:131388253G>T | c.6260G>T | c.(6259-6261)cGc>cTc | p.R2087L |
| HNSC | 9 | 131388796 | 131388796 | + | Missense_Mutation | SNP | G | G | A | TCGA-HD-A4C1-01A-11D-A24D-08 | TCGA-HD-A4C1-10A-02D-A24F-08 | g.chr9:131388796G>A | c.6391G>A | c.(6391-6393)Gag>Aag | p.E2131K |
| HNSC | 9 | 131388879 | 131388879 | + | Missense_Mutation | SNP | G | G | C | TCGA-CR-6481-01A-11D-1870-08 | TCGA-CR-6481-10A-01D-1870-08 | g.chr9:131388879G>C | c.6474G>C | c.(6472-6474)aaG>aaC | p.K2158N |
| HNSC | 9 | 131394416 | 131394416 | + | Missense_Mutation | SNP | A | A | T | TCGA-P3-A6T7-01A-11D-A34J-08 | TCGA-P3-A6T7-10A-01D-A34M-08 | g.chr9:131394416A>T | c.6758A>T | c.(6757-6759)cAg>cTg | p.Q2253L |
| HNSC | 9 | 131394439 | 131394439 | + | Missense_Mutation | SNP | C | C | G | TCGA-DQ-5625-01A-01D-1870-08 | TCGA-DQ-5625-10A-01D-1870-08 | g.chr9:131394439C>G | c.6781C>G | c.(6781-6783)Cag>Gag | p.Q2261E |
| HNSC | 9 | 131395123 | 131395123 | + | Missense_Mutation | SNP | C | C | G | TCGA-DQ-5625-01A-01D-1870-08 | TCGA-DQ-5625-10A-01D-1870-08 | g.chr9:131395123C>G | c.7182C>G | c.(7180-7182)ttC>ttG | p.F2394L |
| HNSC | 9 | 131395129 | 131395129 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-A6K2-01A-11D-A31L-08 | TCGA-CV-A6K2-10A-01D-A31J-08 | g.chr9:131395129C>G | c.7188C>G | c.(7186-7188)atC>atG | p.I2396M |
| KICH | 9 | 131329101 | 131329101 | + | Missense_Mutation | SNP | C | C | T | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr9:131329101C>T | c.82C>T | c.(82-84)Cgc>Tgc | p.R28C |
| KICH | 9 | 131388829 | 131388829 | + | Missense_Mutation | SNP | T | T | C | TCGA-KL-8340-01A-11D-2310-10 | TCGA-KL-8340-11A-01D-2310-10 | g.chr9:131388829T>C | c.6424T>C | c.(6424-6426)Tct>Cct | p.S2142P |
| KIPAN | 9 | 131329101 | 131329101 | + | Missense_Mutation | SNP | C | C | T | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr9:131329101C>T | c.82C>T | c.(82-84)Cgc>Tgc | p.R28C |
| KIPAN | 9 | 131331096 | 131331096 | + | Missense_Mutation | SNP | A | A | T | TCGA-CW-6090-01A-11D-1669-08 | TCGA-CW-6090-11A-01D-1669-08 | g.chr9:131331096A>T | c.283A>T | c.(283-285)Aac>Tac | p.N95Y |
| KIPAN | 9 | 131339498 | 131339498 | + | Silent | SNP | T | T | C | TCGA-B1-5398-01A-02D-1589-08 | TCGA-B1-5398-10A-01D-1589-08 | g.chr9:131339498T>C | c.876T>C | c.(874-876)gcT>gcC | p.A292A |
| KIPAN | 9 | 131343279 | 131343279 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-4807-01A-01D-1373-10 | TCGA-BP-4807-11A-01D-1373-10 | g.chr9:131343279G>T | c.1402G>T | c.(1402-1404)Gac>Tac | p.D468Y |
| KIPAN | 9 | 131345086 | 131345086 | + | Missense_Mutation | SNP | G | G | C | TCGA-B0-5109-01A-02D-1421-08 | TCGA-B0-5109-11A-01D-1421-08 | g.chr9:131345086G>C | c.1764G>C | c.(1762-1764)tgG>tgC | p.W588C |
| KIPAN | 9 | 131361264 | 131361264 | + | Splice_Site | SNP | G | G | T | TCGA-DZ-6135-01A-11D-1961-08 | TCGA-DZ-6135-10A-01D-1962-08 | g.chr9:131361264G>T | c.3542G>T | c.(3541-3543)aGg>aTg | p.R1181M |
| KIPAN | 9 | 131362363 | 131362363 | + | Missense_Mutation | SNP | A | A | T | TCGA-HE-A5NF-01A-11D-A26P-10 | TCGA-HE-A5NF-10A-01D-A26P-10 | g.chr9:131362363A>T | c.3548A>T | c.(3547-3549)gAa>gTa | p.E1183V |
| KIPAN | 9 | 131370474 | 131370474 | + | Silent | SNP | C | C | A | TCGA-DZ-6133-01A-11D-1961-08 | TCGA-DZ-6133-10A-01D-1962-08 | g.chr9:131370474C>A | c.4410C>A | c.(4408-4410)acC>acA | p.T1470T |
| KIPAN | 9 | 131371420 | 131371420 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CJ-4638-01A-02D-1386-10 | TCGA-CJ-4638-11A-01D-1251-10 | g.chr9:131371420C>T | c.4615C>T | c.(4615-4617)Cag>Tag | p.Q1539* |
| KIPAN | 9 | 131374049 | 131374049 | + | Silent | SNP | G | G | A | TCGA-CZ-4857-01A-01D-1373-10 | TCGA-CZ-4857-11A-01D-1373-10 | g.chr9:131374049G>A | c.4815G>A | c.(4813-4815)cgG>cgA | p.R1605R |
| KIPAN | 9 | 131374053 | 131374053 | + | Missense_Mutation | SNP | C | C | G | TCGA-CZ-4857-01A-01D-1373-10 | TCGA-CZ-4857-11A-01D-1373-10 | g.chr9:131374053C>G | c.4819C>G | c.(4819-4821)Cgt>Ggt | p.R1607G |
| KIPAN | 9 | 131379924 | 131379924 | + | Missense_Mutation | SNP | A | A | G | TCGA-A4-A5Y1-01A-11D-A28G-10 | TCGA-A4-A5Y1-11A-11D-A28G-10 | g.chr9:131379924A>G | c.5348A>G | c.(5347-5349)aAg>aGg | p.K1783R |
| KIPAN | 9 | 131386741 | 131386741 | + | Silent | SNP | G | G | A | TCGA-HE-A5NI-01A-11D-A26P-10 | TCGA-HE-A5NI-10A-01D-A26P-10 | g.chr9:131386741G>A | c.5952G>A | c.(5950-5952)aaG>aaA | p.K1984K |
| KIPAN | 9 | 131388829 | 131388829 | + | Missense_Mutation | SNP | T | T | C | TCGA-KL-8340-01A-11D-2310-10 | TCGA-KL-8340-11A-01D-2310-10 | g.chr9:131388829T>C | c.6424T>C | c.(6424-6426)Tct>Cct | p.S2142P |
| KIRC | 9 | 131331096 | 131331096 | + | Missense_Mutation | SNP | A | A | T | TCGA-CW-6090-01A-11D-1669-08 | TCGA-CW-6090-11A-01D-1669-08 | g.chr9:131331096A>T | c.283A>T | c.(283-285)Aac>Tac | p.N95Y |
| KIRC | 9 | 131343279 | 131343279 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-4807-01A-01D-1373-10 | TCGA-BP-4807-11A-01D-1373-10 | g.chr9:131343279G>T | c.1402G>T | c.(1402-1404)Gac>Tac | p.D468Y |
| KIRC | 9 | 131345086 | 131345086 | + | Missense_Mutation | SNP | G | G | C | TCGA-B0-5109-01A-02D-1421-08 | TCGA-B0-5109-11A-01D-1421-08 | g.chr9:131345086G>C | c.1764G>C | c.(1762-1764)tgG>tgC | p.W588C |
| KIRC | 9 | 131371420 | 131371420 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CJ-4638-01A-02D-1386-10 | TCGA-CJ-4638-11A-01D-1251-10 | g.chr9:131371420C>T | c.4615C>T | c.(4615-4617)Cag>Tag | p.Q1539* |
| KIRC | 9 | 131374049 | 131374049 | + | Silent | SNP | G | G | A | TCGA-CZ-4857-01A-01D-1373-10 | TCGA-CZ-4857-11A-01D-1373-10 | g.chr9:131374049G>A | c.4815G>A | c.(4813-4815)cgG>cgA | p.R1605R |
| KIRC | 9 | 131374053 | 131374053 | + | Missense_Mutation | SNP | C | C | G | TCGA-CZ-4857-01A-01D-1373-10 | TCGA-CZ-4857-11A-01D-1373-10 | g.chr9:131374053C>G | c.4819C>G | c.(4819-4821)Cgt>Ggt | p.R1607G |
| KIRP | 9 | 131339498 | 131339498 | + | Silent | SNP | T | T | C | TCGA-B1-5398-01A-02D-1589-08 | TCGA-B1-5398-10A-01D-1589-08 | g.chr9:131339498T>C | c.876T>C | c.(874-876)gcT>gcC | p.A292A |
| KIRP | 9 | 131361264 | 131361264 | + | Splice_Site | SNP | G | G | T | TCGA-DZ-6135-01A-11D-1961-08 | TCGA-DZ-6135-10A-01D-1962-08 | g.chr9:131361264G>T | c.3542G>T | c.(3541-3543)aGg>aTg | p.R1181M |
| KIRP | 9 | 131362363 | 131362363 | + | Missense_Mutation | SNP | A | A | T | TCGA-HE-A5NF-01A-11D-A26P-10 | TCGA-HE-A5NF-10A-01D-A26P-10 | g.chr9:131362363A>T | c.3548A>T | c.(3547-3549)gAa>gTa | p.E1183V |
| KIRP | 9 | 131370474 | 131370474 | + | Silent | SNP | C | C | A | TCGA-DZ-6133-01A-11D-1961-08 | TCGA-DZ-6133-10A-01D-1962-08 | g.chr9:131370474C>A | c.4410C>A | c.(4408-4410)acC>acA | p.T1470T |
| KIRP | 9 | 131379924 | 131379924 | + | Missense_Mutation | SNP | A | A | G | TCGA-A4-A5Y1-01A-11D-A28G-10 | TCGA-A4-A5Y1-11A-11D-A28G-10 | g.chr9:131379924A>G | c.5348A>G | c.(5347-5349)aAg>aGg | p.K1783R |
| KIRP | 9 | 131386741 | 131386741 | + | Silent | SNP | G | G | A | TCGA-HE-A5NI-01A-11D-A26P-10 | TCGA-HE-A5NI-10A-01D-A26P-10 | g.chr9:131386741G>A | c.5952G>A | c.(5950-5952)aaG>aaA | p.K1984K |
| LGG | 9 | 131337005 | 131337005 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DH-5142-01A-01D-1468-08 | TCGA-DH-5142-10A-01D-1468-08 | g.chr9:131337005C>T | c.415C>T | c.(415-417)Cga>Tga | p.R139* |
| LGG | 9 | 131353798 | 131353798 | + | Missense_Mutation | SNP | C | C | T | TCGA-S9-A7R3-01A-11D-A34J-08 | TCGA-S9-A7R3-10A-01D-A34M-08 | g.chr9:131353798C>T | c.3049C>T | c.(3049-3051)Ccg>Tcg | p.P1017S |
| LGG | 9 | 131371422 | 131371422 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr9:131371422G>T | c.4617G>T | c.(4615-4617)caG>caT | p.Q1539H |
| LGG | 9 | 131388217 | 131388217 | + | Missense_Mutation | SNP | G | G | A | TCGA-HT-7875-01A-11D-2395-08 | TCGA-HT-7875-10A-01D-2396-08 | g.chr9:131388217G>A | c.6224G>A | c.(6223-6225)cGc>cAc | p.R2075H |
| LGG | 9 | 131388869 | 131388869 | + | Missense_Mutation | SNP | G | G | A | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr9:131388869G>A | c.6464G>A | c.(6463-6465)cGc>cAc | p.R2155H |
| LIHC | 9 | 131329101 | 131329101 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZS-A9CE-01A-11D-A36X-10 | TCGA-ZS-A9CE-10A-01D-A370-10 | g.chr9:131329101C>T | c.82C>T | c.(82-84)Cgc>Tgc | p.R28C |
| LIHC | 9 | 131337065 | 131337065 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr9:131337065G>T | c.475G>T | c.(475-477)Gag>Tag | p.E159* |
| LIHC | 9 | 131339464 | 131339464 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-A73D-01A-12D-A32G-10 | TCGA-DD-A73D-10A-01D-A32G-10 | g.chr9:131339464A>G | c.842A>G | c.(841-843)gAt>gGt | p.D281G |
| LIHC | 9 | 131339545 | 131339545 | + | Missense_Mutation | SNP | A | A | G | TCGA-2Y-A9H3-01A-11D-A382-10 | TCGA-2Y-A9H3-10A-01D-A385-10 | g.chr9:131339545A>G | c.923A>G | c.(922-924)gAa>gGa | p.E308G |
| LIHC | 9 | 131344805 | 131344805 | + | Silent | SNP | A | A | G | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr9:131344805A>G | c.1620A>G | c.(1618-1620)gcA>gcG | p.A540A |
| LIHC | 9 | 131353846 | 131353846 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-UB-AA0U-01A-11D-A382-10 | TCGA-UB-AA0U-10A-01D-A385-10 | g.chr9:131353846G>T | c.3097G>T | c.(3097-3099)Gag>Tag | p.E1033* |
| LIHC | 9 | 131369944 | 131369944 | + | Missense_Mutation | SNP | G | G | T | TCGA-RC-A6M6-01A-11D-A32G-10 | TCGA-RC-A6M6-10A-01D-A32G-10 | g.chr9:131369944G>T | c.4108G>T | c.(4108-4110)Gat>Tat | p.D1370Y |
| LIHC | 9 | 131374459 | 131374459 | + | Silent | SNP | G | G | C | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr9:131374459G>C | c.4962G>C | c.(4960-4962)ctG>ctC | p.L1654L |
| LIHC | 9 | 131378105 | 131378121 | + | Splice_Site | DEL | GGAGTCCTGGATCAAGT | GGAGTCCTGGATCAAGT | - | TCGA-DD-AADY-01A-11D-A40R-10 | TCGA-DD-AADY-10A-01D-A40U-10 | g.chr9:131378105_131378121delGGAGTCCTGGATCAAGT | c.5328_5342delGGAGTCCTGGATCAAGT | c.(5326-5343)gaggagtcctggatcaag>gag | p.ESWIK1777fs |
| LUAD | 9 | 131331147 | 131331147 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-8302-01A-11D-2323-08 | TCGA-55-8302-10A-01D-2323-08 | g.chr9:131331147G>C | c.334G>C | c.(334-336)Gaa>Caa | p.E112Q |
| LUAD | 9 | 131337584 | 131337584 | + | Missense_Mutation | SNP | G | G | T | TCGA-97-A4M3-01A-11D-A24P-08 | TCGA-97-A4M3-10A-01D-A24P-08 | g.chr9:131337584G>T | c.611G>T | c.(610-612)aGa>aTa | p.R204I |
| LUAD | 9 | 131343323 | 131343323 | + | Missense_Mutation | SNP | G | G | C | TCGA-44-7662-01A-11D-2063-08 | TCGA-44-7662-10A-01D-2063-08 | g.chr9:131343323G>C | c.1446G>C | c.(1444-1446)tgG>tgC | p.W482C |
| LUAD | 9 | 131344062 | 131344062 | + | Splice_Site | SNP | C | C | T | TCGA-80-5607-01A-31D-1945-08 | TCGA-80-5607-10A-01D-1946-08 | g.chr9:131344062C>T | c.1463C>T | c.(1462-1464)gCg>gTg | p.A488V |
| LUAD | 9 | 131344978 | 131344978 | + | Missense_Mutation | SNP | G | G | C | TCGA-91-6836-01A-21D-1855-08 | TCGA-91-6836-11A-01D-1855-08 | g.chr9:131344978G>C | c.1656G>C | c.(1654-1656)ttG>ttC | p.L552F |
| LUAD | 9 | 131345394 | 131345394 | + | Missense_Mutation | SNP | G | G | T | TCGA-49-4488-01A-01D-1753-08 | TCGA-49-4488-11A-01D-1753-08 | g.chr9:131345394G>T | c.1845G>T | c.(1843-1845)caG>caT | p.Q615H |
| LUAD | 9 | 131346727 | 131346727 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-17-Z062-01A-01W-0747-08 | TCGA-17-Z062-11A-01W-0747-08 | g.chr9:131346727delA | c.2360delA | c.(2359-2361)cagfs | p.Q788fs |
| LUAD | 9 | 131347026 | 131347026 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr9:131347026C>G | c.2464C>G | c.(2464-2466)Ctg>Gtg | p.L822V |
| LUAD | 9 | 131347078 | 131347078 | + | Missense_Mutation | SNP | G | G | A | TCGA-05-4415-01A-22D-1855-08 | TCGA-05-4415-10A-01D-1855-08 | g.chr9:131347078G>A | c.2516G>A | c.(2515-2517)cGc>cAc | p.R839H |
| LUAD | 9 | 131348057 | 131348057 | + | Missense_Mutation | SNP | A | A | G | TCGA-17-Z001-01A-01W-0746-08 | TCGA-17-Z001-11A-01W-0746-08 | g.chr9:131348057A>G | c.2591A>G | c.(2590-2592)aAg>aGg | p.K864R |
| LUAD | 9 | 131356466 | 131356466 | + | Silent | SNP | G | G | T | TCGA-49-6767-01A-11D-1855-08 | TCGA-49-6767-11A-01D-1855-08 | g.chr9:131356466G>T | c.3228G>T | c.(3226-3228)ctG>ctT | p.L1076L |
| LUAD | 9 | 131356476 | 131356476 | + | Missense_Mutation | SNP | G | G | T | TCGA-69-A59K-01A-11D-A25L-08 | TCGA-69-A59K-10A-01D-A25L-08 | g.chr9:131356476G>T | c.3238G>T | c.(3238-3240)Ggt>Tgt | p.G1080C |
| LUAD | 9 | 131360769 | 131360769 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8089-01A-11D-2238-08 | TCGA-55-8089-10A-01D-2238-08 | g.chr9:131360769G>T | c.3505G>T | c.(3505-3507)Gct>Tct | p.A1169S |
| LUAD | 9 | 131367432 | 131367432 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-50-6590-01A-12D-1855-08 | TCGA-50-6590-11A-01D-1855-08 | g.chr9:131367432delG | c.3839delG | c.(3838-3840)aggfs | p.R1280fs |
| LUAD | 9 | 131369912 | 131369912 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr9:131369912G>T | c.4076G>T | c.(4075-4077)cGg>cTg | p.R1359L |
| LUAD | 9 | 131369914 | 131369914 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5049-01A-01D-1625-08 | TCGA-50-5049-10A-01D-1625-08 | g.chr9:131369914G>T | c.4078G>T | c.(4078-4080)Ggg>Tgg | p.G1360W |
| LUAD | 9 | 131370275 | 131370275 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-8205-01A-11D-2238-08 | TCGA-55-8205-10A-01D-2238-08 | g.chr9:131370275G>C | c.4291G>C | c.(4291-4293)Gag>Cag | p.E1431Q |
| LUAD | 9 | 131370516 | 131370516 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-6979-01A-11D-1945-08 | TCGA-55-6979-11A-01D-1945-08 | g.chr9:131370516C>G | c.4452C>G | c.(4450-4452)atC>atG | p.I1484M |
| LUAD | 9 | 131371197 | 131371197 | + | Silent | SNP | C | C | T | TCGA-78-7156-01A-11D-2036-08 | TCGA-78-7156-10A-01D-2036-08 | g.chr9:131371197C>T | c.4536C>T | c.(4534-4536)atC>atT | p.I1512I |
| LUAD | 9 | 131371236 | 131371236 | + | Silent | SNP | G | G | T | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr9:131371236G>T | c.4575G>T | c.(4573-4575)cgG>cgT | p.R1525R |
| LUAD | 9 | 131371243 | 131371243 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7537-01A-11D-2063-08 | TCGA-78-7537-10A-01D-2063-08 | g.chr9:131371243G>A | c.4582G>A | c.(4582-4584)Gag>Aag | p.E1528K |
| LUAD | 9 | 131371399 | 131371399 | + | Splice_Site | SNP | A | A | G | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr9:131371399A>G | | c.e36-1 | |
| LUAD | 9 | 131388123 | 131388123 | + | Missense_Mutation | SNP | C | C | G | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr9:131388123C>G | c.6130C>G | c.(6130-6132)Ctc>Gtc | p.L2044V |
| LUAD | 9 | 131390214 | 131390214 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-7911-01A-11D-2167-08 | TCGA-55-7911-10A-01D-2167-08 | g.chr9:131390214C>G | c.6685C>G | c.(6685-6687)Ctc>Gtc | p.L2229V |
| LUAD | 9 | 131395180 | 131395180 | + | Silent | SNP | C | C | T | TCGA-55-7284-01B-11D-2238-08 | TCGA-55-7284-10A-01D-2238-08 | g.chr9:131395180C>T | c.7239C>T | c.(7237-7239)ttC>ttT | p.F2413F |
| LUSC | 9 | 131337068 | 131337068 | + | Missense_Mutation | SNP | G | G | T | TCGA-56-1622-01A-01D-1521-08 | TCGA-56-1622-11A-01D-1521-08 | g.chr9:131337068G>T | c.478G>T | c.(478-480)Gac>Tac | p.D160Y |
| LUSC | 9 | 131339714 | 131339714 | + | Missense_Mutation | SNP | A | A | T | TCGA-60-2709-01A-21D-1817-08 | TCGA-60-2709-11A-01D-1817-08 | g.chr9:131339714A>T | c.1014A>T | c.(1012-1014)gaA>gaT | p.E338D |
| LUSC | 9 | 131345357 | 131345357 | + | Splice_Site | SNP | A | A | G | TCGA-66-2791-01A-01D-0983-08 | TCGA-66-2791-11A-01D-0983-08 | g.chr9:131345357A>G | c.1808A>G | c.(1807-1809)gAt>gGt | p.D603G |
| LUSC | 9 | 131345472 | 131345472 | + | Silent | SNP | C | C | A | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr9:131345472C>A | c.1923C>A | c.(1921-1923)gtC>gtA | p.V641V |
| LUSC | 9 | 131374420 | 131374420 | + | Silent | SNP | G | G | A | TCGA-18-3411-01A-01D-0983-08 | TCGA-18-3411-11A-01D-0983-08 | g.chr9:131374420G>A | c.4923G>A | c.(4921-4923)caG>caA | p.Q1641Q |
| LUSC | 9 | 131381253 | 131381253 | + | Missense_Mutation | SNP | G | G | C | TCGA-21-1077-01A-01D-1521-08 | TCGA-21-1077-11A-01D-1521-08 | g.chr9:131381253G>C | c.5689G>C | c.(5689-5691)Gat>Cat | p.D1897H |
| LUSC | 9 | 131383448 | 131383448 | + | Silent | SNP | G | G | A | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr9:131383448G>A | c.5730G>A | c.(5728-5730)aaG>aaA | p.K1910K |
| OV | 9 | 131329147 | 131329147 | + | Missense_Mutation | SNP | C | C | T | TCGA-61-2012-01A-01W-0722-08 | TCGA-61-2012-11A-01W-0722-08 | g.chr9:131329147C>T | c.128C>T | c.(127-129)tCc>tTc | p.S43F |
| OV | 9 | 131349970 | 131349970 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-13-0920-01A-01W-0421-09 | TCGA-13-0920-10A-01W-0421-09 | g.chr9:131349970delC | c.2864delC | c.(2863-2865)tccfs | p.S955fs |
| OV | 9 | 131360733 | 131360733 | + | Missense_Mutation | SNP | C | C | G | TCGA-61-2102-01A-01W-0722-08 | TCGA-61-2102-11A-01W-0723-08 | g.chr9:131360733C>G | c.3469C>G | c.(3469-3471)Ctg>Gtg | p.L1157V |
| OV | 9 | 131386698 | 131386698 | + | Missense_Mutation | SNP | C | C | T | TCGA-24-1603-01A-01W-0551-08 | TCGA-24-1603-10A-01W-0551-08 | g.chr9:131386698C>T | c.5909C>T | c.(5908-5910)gCg>gTg | p.A1970V |
| PAAD | 9 | 131329137 | 131329137 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:131329137C>T | c.118C>T | c.(118-120)Ctg>Ttg | p.L40L |
| PAAD | 9 | 131365846 | 131365846 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:131365846G>A | c.3604G>A | c.(3604-3606)Gtg>Atg | p.V1202M |
| PAAD | 9 | 131369983 | 131369983 | + | Splice_Site | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:131369983G>A | | c.e32+1 | |
| PRAD | 9 | 131370160 | 131370160 | + | Silent | SNP | T | T | G | TCGA-V1-A9Z8-01A-11D-A41K-08 | TCGA-V1-A9Z8-10A-01D-A41N-08 | g.chr9:131370160T>G | c.4176T>G | c.(4174-4176)gcT>gcG | p.A1392A |
| PRAD | 9 | 131370264 | 131370264 | + | Missense_Mutation | SNP | G | G | A | TCGA-EJ-A7NH-01A-12D-A33T-08 | TCGA-EJ-A7NH-10A-01D-A33W-08 | g.chr9:131370264G>A | c.4280G>A | c.(4279-4281)cGt>cAt | p.R1427H |
| PRAD | 9 | 131381261 | 131381261 | + | Silent | SNP | C | C | T | TCGA-J9-A52C-01A-11D-A26M-08 | TCGA-J9-A52C-10A-01D-A26K-08 | g.chr9:131381261C>T | c.5697C>T | c.(5695-5697)ggC>ggT | p.G1899G |
| PRAD | 9 | 131394422 | 131394422 | + | Missense_Mutation | SNP | T | T | G | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr9:131394422T>G | c.6764T>G | c.(6763-6765)aTc>aGc | p.I2255S |
| READ | 9 | 131329190 | 131329190 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:131329190G>T | c.171G>T | c.(169-171)gaG>gaT | p.E57D |
| READ | 9 | 131346721 | 131346721 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3587-01A-01W-0831-10 | TCGA-AG-3587-10A-01W-0831-10 | g.chr9:131346721G>A | c.2354G>A | c.(2353-2355)cGg>cAg | p.R785Q |
| READ | 9 | 131353800 | 131353800 | + | Silent | SNP | G | G | A | TCGA-DY-A1H8-01A-21D-A152-10 | TCGA-DY-A1H8-10A-01D-A152-10 | g.chr9:131353800G>A | c.3051G>A | c.(3049-3051)ccG>ccA | p.P1017P |
| READ | 9 | 131370209 | 131370209 | + | Missense_Mutation | SNP | G | G | A | TCGA-DY-A1DC-01A-31D-A152-10 | TCGA-DY-A1DC-10A-01D-A152-10 | g.chr9:131370209G>A | c.4225G>A | c.(4225-4227)Gga>Aga | p.G1409R |
| READ | 9 | 131374463 | 131374463 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:131374463G>T | c.4966G>T | c.(4966-4968)Gaa>Taa | p.E1656* |
| READ | 9 | 131379971 | 131379971 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr9:131379971G>A | c.5395G>A | c.(5395-5397)Gtg>Atg | p.V1799M |
| READ | 9 | 131389742 | 131389742 | + | Silent | SNP | C | C | T | TCGA-DY-A1DG-01A-11D-A152-10 | TCGA-DY-A1DG-10A-01D-A152-10 | g.chr9:131389742C>T | c.6639C>T | c.(6637-6639)caC>caT | p.H2213H |
| SARC | 9 | 131347005 | 131347019 | + | In_Frame_Del | DEL | GATTTAATTGGGGTC | GATTTAATTGGGGTC | - | TCGA-DX-AB2O-01A-12D-A38Z-09 | TCGA-DX-AB2O-10A-01D-A38Z-09 | g.chr9:131347005_131347019delGATTTAATTGGGGTC | c.2443_2457delGATTTAATTGGGGTC | c.(2443-2457)gatttaattggggtcdel | p.DLIGV815del |
| SARC | 9 | 131347022 | 131347027 | + | In_Frame_Del | DEL | GAATCT | GAATCT | - | TCGA-DX-AB2O-01A-12D-A38Z-09 | TCGA-DX-AB2O-10A-01D-A38Z-09 | g.chr9:131347022_131347027delGAATCT | c.2460_2465delGAATCT | c.(2458-2466)cagaatctg>cag | p.NL821del |
| SARC | 9 | 131378035 | 131378035 | + | Missense_Mutation | SNP | C | C | T | TCGA-X6-A8C5-01A-11D-A36J-09 | TCGA-X6-A8C5-10A-01D-A36M-09 | g.chr9:131378035C>T | c.5258C>T | c.(5257-5259)gCg>gTg | p.A1753V |
| SKCM | 9 | 131329157 | 131329157 | + | Silent | SNP | C | C | T | TCGA-EE-A2GN-06A-11D-A196-08 | TCGA-EE-A2GN-10A-01D-A198-08 | g.chr9:131329157C>T | c.138C>T | c.(136-138)ttC>ttT | p.F46F |
| SKCM | 9 | 131329158 | 131329158 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A2GN-06A-11D-A196-08 | TCGA-EE-A2GN-10A-01D-A198-08 | g.chr9:131329158C>T | c.139C>T | c.(139-141)Cag>Tag | p.Q47* |
| SKCM | 9 | 131337034 | 131337034 | + | Silent | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr9:131337034C>T | c.444C>T | c.(442-444)gcC>gcT | p.A148A |
| SKCM | 9 | 131339657 | 131339657 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr9:131339657C>T | c.957C>T | c.(955-957)gaC>gaT | p.D319D |
| SKCM | 9 | 131339676 | 131339676 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr9:131339676C>T | c.976C>T | c.(976-978)Cct>Tct | p.P326S |
| SKCM | 9 | 131344084 | 131344084 | + | Missense_Mutation | SNP | G | G | T | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr9:131344084G>T | c.1485G>T | c.(1483-1485)ttG>ttT | p.L495F |
| SKCM | 9 | 131344997 | 131344997 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GT-06A-12D-A197-08 | TCGA-EE-A2GT-10A-01D-A199-08 | g.chr9:131344997C>T | c.1675C>T | c.(1675-1677)Cac>Tac | p.H559Y |
| SKCM | 9 | 131345360 | 131345360 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3C8-06A-12D-A19A-08 | TCGA-D3-A3C8-10A-01D-A19A-08 | g.chr9:131345360C>T | c.1811C>T | c.(1810-1812)cCa>cTa | p.P604L |
| SKCM | 9 | 131346081 | 131346081 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A5GU-06A-11D-A27K-08 | TCGA-D3-A5GU-10A-01D-A27N-08 | g.chr9:131346081G>A | c.2026G>A | c.(2026-2028)Gaa>Aaa | p.E676K |
| SKCM | 9 | 131346163 | 131346163 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr9:131346163C>T | c.2108C>T | c.(2107-2109)tCg>tTg | p.S703L |
| SKCM | 9 | 131353841 | 131353841 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GN-06A-11D-A27K-08 | TCGA-D3-A5GN-10A-01D-A27N-08 | g.chr9:131353841C>T | c.3092C>T | c.(3091-3093)tCc>tTc | p.S1031F |
| SKCM | 9 | 131353854 | 131353854 | + | Silent | SNP | C | C | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr9:131353854C>T | c.3105C>T | c.(3103-3105)ctC>ctT | p.L1035L |
| SKCM | 9 | 131370322 | 131370322 | + | Silent | SNP | A | A | G | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr9:131370322A>G | c.4338A>G | c.(4336-4338)gaA>gaG | p.E1446E |
| SKCM | 9 | 131371229 | 131371229 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr9:131371229C>T | c.4568C>T | c.(4567-4569)tCt>tTt | p.S1523F |
| SKCM | 9 | 131375669 | 131375669 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr9:131375669C>T | c.5038C>T | c.(5038-5040)Ctg>Ttg | p.L1680L |
| SKCM | 9 | 131379952 | 131379952 | + | Silent | SNP | C | C | T | TCGA-EE-A2GU-06A-11D-A196-08 | TCGA-EE-A2GU-10A-01D-A198-08 | g.chr9:131379952C>T | c.5376C>T | c.(5374-5376)taC>taT | p.Y1792Y |
| SKCM | 9 | 131390214 | 131390214 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr9:131390214C>T | c.6685C>T | c.(6685-6687)Ctc>Ttc | p.L2229F |
| SKCM | 9 | 131395598 | 131395598 | + | Silent | SNP | G | G | A | TCGA-EE-A2GM-06B-11D-A196-08 | TCGA-EE-A2GM-10A-01D-A198-08 | g.chr9:131395598G>A | c.7404G>A | c.(7402-7404)tcG>tcA | p.S2468S |