| 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 | 14 | 20845643 | 20845643 | + | Missense_Mutation | SNP | C | C | A | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr14:20845643C>A | c.5884G>T | c.(5884-5886)Ggg>Tgg | p.G1962W |
| ACC | 14 | 20869174 | 20869174 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-OR-A5L2-01A-11D-A30A-10 | TCGA-OR-A5L2-10A-01D-A30A-10 | g.chr14:20869174delC | c.1518delG | c.(1516-1518)gggfs | p.G506fs |
| BLCA | 14 | 20836992 | 20836992 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A5BX-01A-11D-A26M-08 | TCGA-FD-A5BX-10A-01D-A26K-08 | g.chr14:20836992C>G | c.7726G>C | c.(7726-7728)Gat>Cat | p.D2576H |
| BLCA | 14 | 20837594 | 20837594 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-AA6P-01A-11D-A391-08 | TCGA-DK-AA6P-10A-01D-A394-08 | g.chr14:20837594G>C | c.7565C>G | c.(7564-7566)tCt>tGt | p.S2522C |
| BLCA | 14 | 20837625 | 20837625 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-A9T6-01A-11D-A42E-08 | TCGA-XF-A9T6-10A-01D-A42H-08 | g.chr14:20837625G>C | c.7534C>G | c.(7534-7536)Cca>Gca | p.P2512A |
| BLCA | 14 | 20841487 | 20841487 | + | Silent | SNP | G | G | A | TCGA-BT-A0YX-01A-11D-A10S-08 | TCGA-BT-A0YX-10A-01D-A10S-08 | g.chr14:20841487G>A | c.6756C>T | c.(6754-6756)ctC>ctT | p.L2252L |
| BLCA | 14 | 20841685 | 20841685 | + | Missense_Mutation | SNP | C | C | A | TCGA-DK-AA6R-01A-11D-A42E-08 | TCGA-DK-AA6R-10A-01D-A42H-08 | g.chr14:20841685C>A | c.6662G>T | c.(6661-6663)cGg>cTg | p.R2221L |
| BLCA | 14 | 20845844 | 20845844 | + | Silent | SNP | G | G | A | TCGA-GC-A6I1-01A-12D-A31L-08 | TCGA-GC-A6I1-10A-01D-A31J-08 | g.chr14:20845844G>A | c.5790C>T | c.(5788-5790)gcC>gcT | p.A1930A |
| BLCA | 14 | 20848088 | 20848088 | + | Splice_Site | SNP | C | C | A | TCGA-G2-A2ES-01A-11D-A17V-08 | TCGA-G2-A2ES-11A-31D-A17V-08 | g.chr14:20848088C>A | | c.e35+1 | |
| BLCA | 14 | 20848600 | 20848600 | + | Silent | SNP | G | G | A | TCGA-G2-A3IE-01A-11D-A20D-08 | TCGA-G2-A3IE-10A-01D-A20D-08 | g.chr14:20848600G>A | c.4797C>T | c.(4795-4797)ccC>ccT | p.P1599P |
| BLCA | 14 | 20850179 | 20850179 | + | Silent | SNP | C | C | T | TCGA-5N-A9KM-01A-11D-A42E-08 | TCGA-5N-A9KM-10A-01D-A42H-08 | g.chr14:20850179C>T | c.4317G>A | c.(4315-4317)cgG>cgA | p.R1439R |
| BLCA | 14 | 20851967 | 20851967 | + | Silent | SNP | G | G | A | TCGA-GC-A6I1-01A-12D-A31L-08 | TCGA-GC-A6I1-10A-01D-A31J-08 | g.chr14:20851967G>A | c.3645C>T | c.(3643-3645)ctC>ctT | p.L1215L |
| BLCA | 14 | 20852018 | 20852018 | + | Silent | SNP | G | G | A | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr14:20852018G>A | c.3594C>T | c.(3592-3594)ttC>ttT | p.F1198F |
| BLCA | 14 | 20852559 | 20852559 | + | Silent | SNP | G | G | A | TCGA-XF-A9T5-01A-11D-A42E-08 | TCGA-XF-A9T5-10A-01D-A42H-08 | g.chr14:20852559G>A | c.3330C>T | c.(3328-3330)ctC>ctT | p.L1110L |
| BLCA | 14 | 20852648 | 20852648 | + | Missense_Mutation | SNP | C | C | A | TCGA-YC-A9TC-01A-22D-A391-08 | TCGA-YC-A9TC-10A-01D-A394-08 | g.chr14:20852648C>A | c.3241G>T | c.(3241-3243)Ggt>Tgt | p.G1081C |
| BLCA | 14 | 20852874 | 20852874 | + | Splice_Site | SNP | T | T | G | TCGA-ZF-AA58-01A-12D-A42E-08 | TCGA-ZF-AA58-10A-01D-A42H-08 | g.chr14:20852874T>G | | c.e22-2 | |
| BLCA | 14 | 20853181 | 20853181 | + | Missense_Mutation | SNP | G | G | C | TCGA-K4-A5RI-01A-11D-A289-08 | TCGA-K4-A5RI-10A-01D-A289-08 | g.chr14:20853181G>C | c.3070C>G | c.(3070-3072)Caa>Gaa | p.Q1024E |
| BLCA | 14 | 20856168 | 20856168 | + | Missense_Mutation | SNP | G | G | C | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr14:20856168G>C | c.2580C>G | c.(2578-2580)gaC>gaG | p.D860E |
| BLCA | 14 | 20859211 | 20859211 | + | Silent | SNP | C | C | T | TCGA-GU-AATO-01A-11D-A391-08 | TCGA-GU-AATO-10A-01D-A394-08 | g.chr14:20859211C>T | c.2142G>A | c.(2140-2142)acG>acA | p.T714T |
| BLCA | 14 | 20871547 | 20871547 | + | Missense_Mutation | SNP | C | C | G | TCGA-BT-A2LB-01A-11D-A18F-08 | TCGA-BT-A2LB-10A-01D-A18F-08 | g.chr14:20871547C>G | c.1255G>C | c.(1255-1257)Gag>Cag | p.E419Q |
| BLCA | 14 | 20871889 | 20871889 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr14:20871889C>T | c.1187G>A | c.(1186-1188)cGc>cAc | p.R396H |
| BLCA | 14 | 20871927 | 20871927 | + | Silent | SNP | C | C | T | TCGA-ZF-AA4N-01A-11D-A38G-08 | TCGA-ZF-AA4N-10A-01D-A38J-08 | g.chr14:20871927C>T | c.1149G>A | c.(1147-1149)cgG>cgA | p.R383R |
| BLCA | 14 | 20876196 | 20876196 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A2I2-01A-11D-A17V-08 | TCGA-DK-A2I2-10A-01D-A17V-08 | g.chr14:20876196G>C | c.403C>G | c.(403-405)Cac>Gac | p.H135D |
| BLCA | 14 | 20876254 | 20876254 | + | Silent | SNP | G | G | A | TCGA-BT-A3PH-01A-11D-A21Z-08 | TCGA-BT-A3PH-10A-01D-A21Z-08 | g.chr14:20876254G>A | c.345C>T | c.(343-345)ctC>ctT | p.L115L |
| BLCA | 14 | 20876347 | 20876347 | + | Silent | SNP | T | T | A | TCGA-FJ-A3ZE-01A-11D-A23M-08 | TCGA-FJ-A3ZE-10A-01D-A23K-08 | g.chr14:20876347T>A | c.252A>T | c.(250-252)acA>acT | p.T84T |
| BLCA | 14 | 20876359 | 20876359 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr14:20876359C>G | c.240G>C | c.(238-240)caG>caC | p.Q80H |
| BLCA | 14 | 20876465 | 20876466 | + | Frame_Shift_Ins | INS | - | - | GGATATTC | TCGA-XF-A9ST-01A-11D-A42E-08 | TCGA-XF-A9ST-10A-01D-A42H-08 | g.chr14:20876465_20876466insGGATATTC | c.133_134insGAATATCC | c.(133-135)ctcfs | p.L45fs |
| BRCA | 14 | 20836967 | 20836967 | + | Missense_Mutation | SNP | C | C | T | TCGA-D8-A1XQ-01A-11D-A14K-09 | TCGA-D8-A1XQ-10A-01D-A14K-09 | g.chr14:20836967C>T | c.7751G>A | c.(7750-7752)aGt>aAt | p.S2584N |
| BRCA | 14 | 20837883 | 20837883 | + | Missense_Mutation | SNP | T | T | A | TCGA-BH-A0BZ-01A-31D-A12Q-09 | TCGA-BH-A0BZ-11A-61D-A12Q-09 | g.chr14:20837883T>A | c.7373A>T | c.(7372-7374)gAg>gTg | p.E2458V |
| BRCA | 14 | 20845601 | 20845601 | + | Missense_Mutation | SNP | C | C | A | TCGA-AN-A0FX-01A-11W-A050-09 | TCGA-AN-A0FX-10A-01W-A055-09 | g.chr14:20845601C>A | c.5926G>T | c.(5926-5928)Gcc>Tcc | p.A1976S |
| BRCA | 14 | 20846384 | 20846384 | + | Silent | SNP | T | T | G | TCGA-AN-A0XN-01A-21D-A10G-09 | TCGA-AN-A0XN-10A-01D-A10G-09 | g.chr14:20846384T>G | c.5520A>C | c.(5518-5520)gcA>gcC | p.A1840A |
| BRCA | 14 | 20848488 | 20848488 | + | Missense_Mutation | SNP | G | G | C | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr14:20848488G>C | c.4909C>G | c.(4909-4911)Ctt>Gtt | p.L1637V |
| BRCA | 14 | 20851645 | 20851645 | + | Splice_Site | SNP | A | A | C | TCGA-A2-A0T5-01A-21D-A099-09 | TCGA-A2-A0T5-10A-01D-A099-09 | g.chr14:20851645A>C | | c.e26+1 | |
| BRCA | 14 | 20852245 | 20852245 | + | Missense_Mutation | SNP | C | C | A | TCGA-OL-A66J-01A-11D-A29N-09 | TCGA-OL-A66J-10A-01D-A29N-09 | g.chr14:20852245C>A | c.3486G>T | c.(3484-3486)agG>agT | p.R1162S |
| BRCA | 14 | 20852647 | 20852647 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr14:20852647delC | c.3242delG | c.(3241-3243)ggtfs | p.G1081fs |
| BRCA | 14 | 20856087 | 20856087 | + | Silent | SNP | G | G | C | TCGA-C8-A1HM-01A-12D-A135-09 | TCGA-C8-A1HM-10A-01D-A135-09 | g.chr14:20856087G>C | c.2661C>G | c.(2659-2661)ccC>ccG | p.P887P |
| BRCA | 14 | 20863645 | 20863645 | + | Missense_Mutation | SNP | T | T | G | TCGA-E2-A10B-01A-11D-A10M-09 | TCGA-E2-A10B-10A-01D-A10M-09 | g.chr14:20863645T>G | c.1892A>C | c.(1891-1893)cAg>cCg | p.Q631P |
| BRCA | 14 | 20871929 | 20871929 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A1FU-01A-11D-A14G-09 | TCGA-BH-A1FU-11A-23D-A14G-09 | g.chr14:20871929G>A | c.1147C>T | c.(1147-1149)Cgg>Tgg | p.R383W |
| BRCA | 14 | 20871967 | 20871967 | + | Missense_Mutation | SNP | G | G | A | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr14:20871967G>A | c.1109C>T | c.(1108-1110)gCc>gTc | p.A370V |
| BRCA | 14 | 20872808 | 20872808 | + | Missense_Mutation | SNP | G | G | C | TCGA-A8-A085-01A-11W-A019-09 | TCGA-A8-A085-10A-01W-A021-09 | g.chr14:20872808G>C | c.994C>G | c.(994-996)Ctg>Gtg | p.L332V |
| BRCA | 14 | 20873630 | 20873630 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-C8-A131-01A-11D-A10Y-09 | TCGA-C8-A131-10A-01D-A110-09 | g.chr14:20873630C>A | c.850G>T | c.(850-852)Gag>Tag | p.E284* |
| BRCA | 14 | 20873681 | 20873681 | + | Missense_Mutation | SNP | C | C | T | TCGA-AN-A0XU-01A-11D-A10G-09 | TCGA-AN-A0XU-10A-01D-A10G-09 | g.chr14:20873681C>T | c.799G>A | c.(799-801)Gac>Aac | p.D267N |
| BRCA | 14 | 20874451 | 20874451 | + | Missense_Mutation | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr14:20874451T>G | c.676A>C | c.(676-678)Acc>Ccc | p.T226P |
| BRCA | 14 | 20876196 | 20876196 | + | Missense_Mutation | SNP | G | G | C | TCGA-E9-A1R7-01A-11D-A14K-09 | TCGA-E9-A1R7-10A-01D-A14K-09 | g.chr14:20876196G>C | c.403C>G | c.(403-405)Cac>Gac | p.H135D |
| BRCA | 14 | 20876336 | 20876336 | + | Missense_Mutation | SNP | A | A | T | TCGA-A2-A0D4-01A-11W-A019-09 | TCGA-A2-A0D4-10A-01W-A021-09 | g.chr14:20876336A>T | c.263T>A | c.(262-264)cTg>cAg | p.L88Q |
| CESC | 14 | 20841187 | 20841187 | + | Missense_Mutation | SNP | C | C | A | TCGA-Q1-A73Q-01A-21D-A32I-09 | TCGA-Q1-A73Q-10B-01D-A32I-09 | g.chr14:20841187C>A | c.6934G>T | c.(6934-6936)Gct>Tct | p.A2312S |
| CESC | 14 | 20841447 | 20841447 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EK-A3GN-01A-11D-A20U-09 | TCGA-EK-A3GN-10A-01D-A20U-09 | g.chr14:20841447G>A | c.6796C>T | c.(6796-6798)Cag>Tag | p.Q2266* |
| CESC | 14 | 20842653 | 20842653 | + | Missense_Mutation | SNP | C | C | G | TCGA-IR-A3LL-01A-11D-A20U-09 | TCGA-IR-A3LL-10A-01D-A20U-09 | g.chr14:20842653C>G | c.6406G>C | c.(6406-6408)Gag>Cag | p.E2136Q |
| CESC | 14 | 20845581 | 20845581 | + | Silent | SNP | T | T | A | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chr14:20845581T>A | c.5946A>T | c.(5944-5946)gtA>gtT | p.V1982V |
| CESC | 14 | 20849739 | 20849739 | + | Missense_Mutation | SNP | C | C | G | TCGA-FU-A3HY-01A-11D-A21Q-09 | TCGA-FU-A3HY-10A-01D-A21Q-09 | g.chr14:20849739C>G | c.4531G>C | c.(4531-4533)Gag>Cag | p.E1511Q |
| CESC | 14 | 20852329 | 20852329 | + | Silent | SNP | G | G | A | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr14:20852329G>A | c.3402C>T | c.(3400-3402)ttC>ttT | p.F1134F |
| CESC | 14 | 20852820 | 20852820 | + | Missense_Mutation | SNP | C | C | T | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chr14:20852820C>T | c.3160G>A | c.(3160-3162)Gca>Aca | p.A1054T |
| CESC | 14 | 20854746 | 20854746 | + | Silent | SNP | G | G | A | TCGA-IR-A3LA-01A-11D-A22X-09 | TCGA-IR-A3LA-10A-01D-A22X-09 | g.chr14:20854746G>A | c.2721C>T | c.(2719-2721)ttC>ttT | p.F907F |
| CESC | 14 | 20859825 | 20859825 | + | Missense_Mutation | SNP | C | C | T | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chr14:20859825C>T | c.2030G>A | c.(2029-2031)cGc>cAc | p.R677H |
| CESC | 14 | 20864069 | 20864069 | + | Missense_Mutation | SNP | G | G | C | TCGA-EK-A2H0-01A-11D-A17W-09 | TCGA-EK-A2H0-10A-01D-A17W-09 | g.chr14:20864069G>C | c.1699C>G | c.(1699-1701)Ctt>Gtt | p.L567V |
| CESC | 14 | 20873630 | 20873630 | + | Missense_Mutation | SNP | C | C | G | TCGA-C5-A1BK-01B-11D-A13W-08 | TCGA-C5-A1BK-10A-01D-A13W-08 | g.chr14:20873630C>G | c.850G>C | c.(850-852)Gag>Cag | p.E284Q |
| COAD | 14 | 20836606 | 20836606 | + | Missense_Mutation | SNP | T | T | C | TCGA-AY-6386-01A-21D-1719-10 | TCGA-AY-6386-10A-01D-1719-10 | g.chr14:20836606T>C | c.7874A>G | c.(7873-7875)aAt>aGt | p.N2625S |
| COAD | 14 | 20836631 | 20836631 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6923-01A-11D-1924-10 | TCGA-D5-6923-10A-01D-1924-10 | g.chr14:20836631C>T | c.7849G>A | c.(7849-7851)Gtg>Atg | p.V2617M |
| COAD | 14 | 20837644 | 20837644 | + | Missense_Mutation | SNP | C | C | G | TCGA-D5-6929-01A-31D-1924-10 | TCGA-D5-6929-10A-01D-1924-10 | g.chr14:20837644C>G | c.7515G>C | c.(7513-7515)tgG>tgC | p.W2505C |
| COAD | 14 | 20839723 | 20839723 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr14:20839723C>T | c.7145G>A | c.(7144-7146)gGt>gAt | p.G2382D |
| COAD | 14 | 20840909 | 20840909 | + | Silent | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr14:20840909C>T | c.7059G>A | c.(7057-7059)tcG>tcA | p.S2353S |
| COAD | 14 | 20845812 | 20845812 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr14:20845812C>T | c.5822G>A | c.(5821-5823)cGg>cAg | p.R1941Q |
| COAD | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| COAD | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| COAD | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| COAD | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| COAD | 14 | 20846381 | 20846381 | + | Silent | SNP | G | G | A | TCGA-A6-6137-01A-11D-1771-10 | TCGA-A6-6137-10A-01D-1806-10 | g.chr14:20846381G>A | c.5523C>T | c.(5521-5523)ccC>ccT | p.P1841P |
| COAD | 14 | 20846615 | 20846615 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr14:20846615T>C | c.5432A>G | c.(5431-5433)gAg>gGg | p.E1811G |
| COAD | 14 | 20848443 | 20848443 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2674-01A-02W-0831-10 | TCGA-A6-2674-10A-01W-0831-10 | g.chr14:20848443G>A | c.4954C>T | c.(4954-4956)Cac>Tac | p.H1652Y |
| COAD | 14 | 20848607 | 20848607 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr14:20848607delT | c.4790delA | c.(4789-4791)aagfs | p.K1597fs |
| COAD | 14 | 20849744 | 20849744 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6965-01A-11D-1924-10 | TCGA-AD-6965-10A-01D-1924-10 | g.chr14:20849744C>T | c.4526G>A | c.(4525-4527)gGg>gAg | p.G1509E |
| COAD | 14 | 20849775 | 20849775 | + | Missense_Mutation | SNP | C | C | T | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr14:20849775C>T | c.4495G>A | c.(4495-4497)Gca>Aca | p.A1499T |
| COAD | 14 | 20850836 | 20850836 | + | Silent | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr14:20850836C>T | c.4086G>A | c.(4084-4086)ccG>ccA | p.P1362P |
| COAD | 14 | 20852291 | 20852291 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr14:20852291C>T | c.3440G>A | c.(3439-3441)cGc>cAc | p.R1147H |
| COAD | 14 | 20852601 | 20852601 | + | Silent | SNP | C | C | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr14:20852601C>A | c.3288G>T | c.(3286-3288)ggG>ggT | p.G1096G |
| COAD | 14 | 20852618 | 20852618 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr14:20852618C>T | c.3271G>A | c.(3271-3273)Ggg>Agg | p.G1091R |
| COAD | 14 | 20852647 | 20852647 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr14:20852647delC | c.3242delG | c.(3241-3243)ggtfs | p.G1081fs |
| COAD | 14 | 20854324 | 20854324 | + | Silent | SNP | C | C | T | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr14:20854324C>T | c.2892G>A | c.(2890-2892)gaG>gaA | p.E964E |
| COAD | 14 | 20854650 | 20854650 | + | Silent | SNP | G | G | A | TCGA-A6-4105-01A-02D-1771-10 | TCGA-A6-4105-10A-01D-1771-10 | g.chr14:20854650G>A | c.2817C>T | c.(2815-2817)atC>atT | p.I939I |
| COAD | 14 | 20854727 | 20854727 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr14:20854727G>A | c.2740C>T | c.(2740-2742)Cgg>Tgg | p.R914W |
| COAD | 14 | 20856202 | 20856202 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr14:20856202G>A | c.2546C>T | c.(2545-2547)gCc>gTc | p.A849V |
| COAD | 14 | 20863728 | 20863728 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr14:20863728C>A | c.1809G>T | c.(1807-1809)aaG>aaT | p.K603N |
| COAD | 14 | 20864064 | 20864064 | + | Silent | SNP | G | G | A | TCGA-D5-6920-01A-11D-1924-10 | TCGA-D5-6920-10A-01D-1924-10 | g.chr14:20864064G>A | c.1704C>T | c.(1702-1704)aaC>aaT | p.N568N |
| COAD | 14 | 20864065 | 20864065 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr14:20864065T>C | c.1703A>G | c.(1702-1704)aAc>aGc | p.N568S |
| COAD | 14 | 20864835 | 20864835 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr14:20864835C>T | c.1604G>A | c.(1603-1605)cGg>cAg | p.R535Q |
| COAD | 14 | 20871889 | 20871889 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr14:20871889C>T | c.1187G>A | c.(1186-1188)cGc>cAc | p.R396H |
| COAD | 14 | 20871902 | 20871902 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr14:20871902delG | c.1174delC | c.(1174-1176)cgcfs | p.R393fs |
| COAD | 14 | 20873695 | 20873695 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr14:20873695A>G | c.785T>C | c.(784-786)aTg>aCg | p.M262T |
| COAD | 14 | 20876262 | 20876262 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr14:20876262C>T | c.337G>A | c.(337-339)Gcc>Acc | p.A113T |
| COAD | 14 | 20876271 | 20876271 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr14:20876271G>A | c.328C>T | c.(328-330)Cgg>Tgg | p.R110W |
| COADREAD | 14 | 20836606 | 20836606 | + | Missense_Mutation | SNP | T | T | C | TCGA-AY-6386-01A-21D-1719-10 | TCGA-AY-6386-10A-01D-1719-10 | g.chr14:20836606T>C | c.7874A>G | c.(7873-7875)aAt>aGt | p.N2625S |
| COADREAD | 14 | 20836631 | 20836631 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6923-01A-11D-1924-10 | TCGA-D5-6923-10A-01D-1924-10 | g.chr14:20836631C>T | c.7849G>A | c.(7849-7851)Gtg>Atg | p.V2617M |
| COADREAD | 14 | 20837644 | 20837644 | + | Missense_Mutation | SNP | C | C | G | TCGA-D5-6929-01A-31D-1924-10 | TCGA-D5-6929-10A-01D-1924-10 | g.chr14:20837644C>G | c.7515G>C | c.(7513-7515)tgG>tgC | p.W2505C |
| COADREAD | 14 | 20839723 | 20839723 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr14:20839723C>T | c.7145G>A | c.(7144-7146)gGt>gAt | p.G2382D |
| COADREAD | 14 | 20840909 | 20840909 | + | Silent | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr14:20840909C>T | c.7059G>A | c.(7057-7059)tcG>tcA | p.S2353S |
| COADREAD | 14 | 20845812 | 20845812 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr14:20845812C>T | c.5822G>A | c.(5821-5823)cGg>cAg | p.R1941Q |
| COADREAD | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| COADREAD | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| COADREAD | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| COADREAD | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| COADREAD | 14 | 20846381 | 20846381 | + | Silent | SNP | G | G | A | TCGA-A6-6137-01A-11D-1771-10 | TCGA-A6-6137-10A-01D-1806-10 | g.chr14:20846381G>A | c.5523C>T | c.(5521-5523)ccC>ccT | p.P1841P |
| COADREAD | 14 | 20846615 | 20846615 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr14:20846615T>C | c.5432A>G | c.(5431-5433)gAg>gGg | p.E1811G |
| COADREAD | 14 | 20848443 | 20848443 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2674-01A-02W-0831-10 | TCGA-A6-2674-10A-01W-0831-10 | g.chr14:20848443G>A | c.4954C>T | c.(4954-4956)Cac>Tac | p.H1652Y |
| COADREAD | 14 | 20848607 | 20848607 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr14:20848607delT | c.4790delA | c.(4789-4791)aagfs | p.K1597fs |
| COADREAD | 14 | 20849744 | 20849744 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6965-01A-11D-1924-10 | TCGA-AD-6965-10A-01D-1924-10 | g.chr14:20849744C>T | c.4526G>A | c.(4525-4527)gGg>gAg | p.G1509E |
| COADREAD | 14 | 20849775 | 20849775 | + | Missense_Mutation | SNP | C | C | T | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr14:20849775C>T | c.4495G>A | c.(4495-4497)Gca>Aca | p.A1499T |
| COADREAD | 14 | 20850836 | 20850836 | + | Silent | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr14:20850836C>T | c.4086G>A | c.(4084-4086)ccG>ccA | p.P1362P |
| COADREAD | 14 | 20852291 | 20852291 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr14:20852291C>T | c.3440G>A | c.(3439-3441)cGc>cAc | p.R1147H |
| COADREAD | 14 | 20852601 | 20852601 | + | Silent | SNP | C | C | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr14:20852601C>A | c.3288G>T | c.(3286-3288)ggG>ggT | p.G1096G |
| COADREAD | 14 | 20852618 | 20852618 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr14:20852618C>T | c.3271G>A | c.(3271-3273)Ggg>Agg | p.G1091R |
| COADREAD | 14 | 20852647 | 20852647 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr14:20852647delC | c.3242delG | c.(3241-3243)ggtfs | p.G1081fs |
| COADREAD | 14 | 20854324 | 20854324 | + | Silent | SNP | C | C | T | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr14:20854324C>T | c.2892G>A | c.(2890-2892)gaG>gaA | p.E964E |
| COADREAD | 14 | 20854650 | 20854650 | + | Silent | SNP | G | G | A | TCGA-A6-4105-01A-02D-1771-10 | TCGA-A6-4105-10A-01D-1771-10 | g.chr14:20854650G>A | c.2817C>T | c.(2815-2817)atC>atT | p.I939I |
| COADREAD | 14 | 20854727 | 20854727 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr14:20854727G>A | c.2740C>T | c.(2740-2742)Cgg>Tgg | p.R914W |
| COADREAD | 14 | 20856202 | 20856202 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr14:20856202G>A | c.2546C>T | c.(2545-2547)gCc>gTc | p.A849V |
| COADREAD | 14 | 20857405 | 20857405 | + | Silent | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr14:20857405C>T | c.2517G>A | c.(2515-2517)gcG>gcA | p.A839A |
| COADREAD | 14 | 20859205 | 20859205 | + | Silent | SNP | C | C | T | TCGA-CL-5917-01A-11D-1657-10 | TCGA-CL-5917-10A-01D-1657-10 | g.chr14:20859205C>T | c.2148G>A | c.(2146-2148)gcG>gcA | p.A716A |
| COADREAD | 14 | 20863728 | 20863728 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr14:20863728C>A | c.1809G>T | c.(1807-1809)aaG>aaT | p.K603N |
| COADREAD | 14 | 20864064 | 20864064 | + | Silent | SNP | G | G | A | TCGA-D5-6920-01A-11D-1924-10 | TCGA-D5-6920-10A-01D-1924-10 | g.chr14:20864064G>A | c.1704C>T | c.(1702-1704)aaC>aaT | p.N568N |
| COADREAD | 14 | 20864065 | 20864065 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr14:20864065T>C | c.1703A>G | c.(1702-1704)aAc>aGc | p.N568S |
| COADREAD | 14 | 20864835 | 20864835 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr14:20864835C>T | c.1604G>A | c.(1603-1605)cGg>cAg | p.R535Q |
| COADREAD | 14 | 20871889 | 20871889 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr14:20871889C>T | c.1187G>A | c.(1186-1188)cGc>cAc | p.R396H |
| COADREAD | 14 | 20871902 | 20871902 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr14:20871902delG | c.1174delC | c.(1174-1176)cgcfs | p.R393fs |
| COADREAD | 14 | 20873695 | 20873695 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr14:20873695A>G | c.785T>C | c.(784-786)aTg>aCg | p.M262T |
| COADREAD | 14 | 20876262 | 20876262 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr14:20876262C>T | c.337G>A | c.(337-339)Gcc>Acc | p.A113T |
| COADREAD | 14 | 20876271 | 20876271 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr14:20876271G>A | c.328C>T | c.(328-330)Cgg>Tgg | p.R110W |
| DLBC | 14 | 20871901 | 20871901 | + | Missense_Mutation | SNP | C | C | T | TCGA-G8-6914-01A-11D-2210-10 | TCGA-G8-6914-14A-01D-2210-10 | g.chr14:20871901C>T | c.1175G>A | c.(1174-1176)cGc>cAc | p.R392H |
| DLBC | 14 | 20873695 | 20873695 | + | Missense_Mutation | SNP | A | A | G | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr14:20873695A>G | c.785T>C | c.(784-786)aTg>aCg | p.M262T |
| ESCA | 14 | 20844365 | 20844365 | + | Silent | SNP | T | T | C | TCGA-L5-A88S-01A-11D-A36J-09 | TCGA-L5-A88S-11A-21D-A36M-09 | g.chr14:20844365T>C | c.6147A>G | c.(6145-6147)gaA>gaG | p.E2049E |
| ESCA | 14 | 20845785 | 20845785 | + | Missense_Mutation | SNP | C | C | A | TCGA-L5-A43J-01A-12D-A247-09 | TCGA-L5-A43J-11A-11D-A247-09 | g.chr14:20845785C>A | c.5849G>T | c.(5848-5850)gGc>gTc | p.G1950V |
| ESCA | 14 | 20851740 | 20851740 | + | Silent | SNP | G | G | T | TCGA-IG-A4QT-01A-21D-A27G-09 | TCGA-IG-A4QT-10A-02D-A27G-09 | g.chr14:20851740G>T | c.3774C>A | c.(3772-3774)ggC>ggA | p.G1258G |
| ESCA | 14 | 20876111 | 20876111 | + | Missense_Mutation | SNP | G | G | A | TCGA-XP-A8T6-01A-11D-A36J-09 | TCGA-XP-A8T6-10A-01D-A36M-09 | g.chr14:20876111G>A | c.488C>T | c.(487-489)tCt>tTt | p.S163F |
| GBM | 14 | 20841727 | 20841727 | + | Missense_Mutation | SNP | G | G | A | TCGA-14-0740-01B-01D-1845-08 | TCGA-14-0740-10B-01D-1845-08 | g.chr14:20841727G>A | c.6620C>T | c.(6619-6621)tCa>tTa | p.S2207L |
| GBM | 14 | 20846241 | 20846241 | + | Missense_Mutation | SNP | G | G | A | TCGA-87-5896-01A-01D-1696-08 | TCGA-87-5896-10A-01D-1696-08 | g.chr14:20846241G>A | c.5663C>T | c.(5662-5664)gCt>gTt | p.A1888V |
| GBM | 14 | 20848171 | 20848171 | + | Missense_Mutation | SNP | A | A | G | TCGA-06-5413-01A-01D-1696-08 | TCGA-06-5413-10A-01D-1696-08 | g.chr14:20848171A>G | c.5045T>C | c.(5044-5046)gTg>gCg | p.V1682A |
| GBM | 14 | 20871545 | 20871545 | + | Silent | SNP | C | C | T | TCGA-14-1450-01B-01D-1845-08 | TCGA-14-1450-10B-01D-1845-08 | g.chr14:20871545C>T | c.1257G>A | c.(1255-1257)gaG>gaA | p.E419E |
| GBM | 14 | 20873722 | 20873722 | + | Missense_Mutation | SNP | C | C | G | TCGA-19-5955-01A-11D-1696-08 | TCGA-19-5955-11A-01D-1696-08 | g.chr14:20873722C>G | c.758G>C | c.(757-759)tGc>tCc | p.C253S |
| GBM | 14 | 20873724 | 20873724 | + | Silent | SNP | C | C | G | TCGA-19-5955-01A-11D-1696-08 | TCGA-19-5955-11A-01D-1696-08 | g.chr14:20873724C>G | c.756G>C | c.(754-756)ctG>ctC | p.L252L |
| GBMLGG | 14 | 20841727 | 20841727 | + | Missense_Mutation | SNP | G | G | A | TCGA-14-0740-01B-01D-1845-08 | TCGA-14-0740-10B-01D-1845-08 | g.chr14:20841727G>A | c.6620C>T | c.(6619-6621)tCa>tTa | p.S2207L |
| GBMLGG | 14 | 20845586 | 20845586 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20845586T>C | c.5941A>G | c.(5941-5943)Aag>Gag | p.K1981E |
| GBMLGG | 14 | 20845812 | 20845812 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20845812C>T | c.5822G>A | c.(5821-5823)cGg>cAg | p.R1941Q |
| GBMLGG | 14 | 20846220 | 20846220 | + | Missense_Mutation | SNP | G | G | A | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr14:20846220G>A | c.5684C>T | c.(5683-5685)gCg>gTg | p.A1895V |
| GBMLGG | 14 | 20846241 | 20846241 | + | Missense_Mutation | SNP | G | G | A | TCGA-87-5896-01A-01D-1696-08 | TCGA-87-5896-10A-01D-1696-08 | g.chr14:20846241G>A | c.5663C>T | c.(5662-5664)gCt>gTt | p.A1888V |
| GBMLGG | 14 | 20848171 | 20848171 | + | Missense_Mutation | SNP | A | A | G | TCGA-06-5413-01A-01D-1696-08 | TCGA-06-5413-10A-01D-1696-08 | g.chr14:20848171A>G | c.5045T>C | c.(5044-5046)gTg>gCg | p.V1682A |
| GBMLGG | 14 | 20850092 | 20850092 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20850092G>A | c.4404C>T | c.(4402-4404)tgC>tgT | p.C1468C |
| GBMLGG | 14 | 20851712 | 20851712 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20851712C>T | c.3802G>A | c.(3802-3804)Gct>Act | p.A1268T |
| GBMLGG | 14 | 20852291 | 20852291 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20852291C>T | c.3440G>A | c.(3439-3441)cGc>cAc | p.R1147H |
| GBMLGG | 14 | 20852762 | 20852762 | + | Missense_Mutation | SNP | C | C | T | TCGA-TM-A7C4-01A-11D-A32B-08 | TCGA-TM-A7C4-10A-01D-A329-08 | g.chr14:20852762C>T | c.3218G>A | c.(3217-3219)cGc>cAc | p.R1073H |
| GBMLGG | 14 | 20854314 | 20854314 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20854314G>A | c.2902C>T | c.(2902-2904)Ctg>Ttg | p.L968L |
| GBMLGG | 14 | 20854643 | 20854643 | + | Missense_Mutation | SNP | G | G | A | TCGA-P5-A5EZ-01A-11D-A27K-08 | TCGA-P5-A5EZ-10A-01D-A27N-08 | g.chr14:20854643G>A | c.2824C>T | c.(2824-2826)Cgc>Tgc | p.R942C |
| GBMLGG | 14 | 20871545 | 20871545 | + | Silent | SNP | C | C | T | TCGA-14-1450-01B-01D-1845-08 | TCGA-14-1450-10B-01D-1845-08 | g.chr14:20871545C>T | c.1257G>A | c.(1255-1257)gaG>gaA | p.E419E |
| GBMLGG | 14 | 20871901 | 20871901 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20871901C>T | c.1175G>A | c.(1174-1176)cGc>cAc | p.R392H |
| GBMLGG | 14 | 20873722 | 20873722 | + | Missense_Mutation | SNP | C | C | G | TCGA-19-5955-01A-11D-1696-08 | TCGA-19-5955-11A-01D-1696-08 | g.chr14:20873722C>G | c.758G>C | c.(757-759)tGc>tCc | p.C253S |
| GBMLGG | 14 | 20873724 | 20873724 | + | Silent | SNP | C | C | G | TCGA-19-5955-01A-11D-1696-08 | TCGA-19-5955-11A-01D-1696-08 | g.chr14:20873724C>G | c.756G>C | c.(754-756)ctG>ctC | p.L252L |
| HNSC | 14 | 20836610 | 20836610 | + | Missense_Mutation | SNP | G | G | T | TCGA-P3-A5QF-01A-11D-A28R-08 | TCGA-P3-A5QF-10A-01D-A28U-08 | g.chr14:20836610G>T | c.7870C>A | c.(7870-7872)Ctg>Atg | p.L2624M |
| HNSC | 14 | 20836706 | 20836706 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-F7-A620-01A-11D-A28R-08 | TCGA-F7-A620-10A-01D-A28U-08 | g.chr14:20836706G>A | c.7774C>T | c.(7774-7776)Cga>Tga | p.R2592* |
| HNSC | 14 | 20836999 | 20836999 | + | Silent | SNP | C | C | T | TCGA-CN-A63T-01A-11D-A28R-08 | TCGA-CN-A63T-10A-01D-A28U-08 | g.chr14:20836999C>T | c.7719G>A | c.(7717-7719)aaG>aaA | p.K2573K |
| HNSC | 14 | 20837659 | 20837659 | + | Silent | SNP | G | G | A | TCGA-CV-7418-01A-11D-2078-08 | TCGA-CV-7418-10A-01D-2078-08 | g.chr14:20837659G>A | c.7500C>T | c.(7498-7500)acC>acT | p.T2500T |
| HNSC | 14 | 20841549 | 20841549 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A6JE-01A-11D-A31L-08 | TCGA-CV-A6JE-10A-01D-A31J-08 | g.chr14:20841549G>A | c.6694C>T | c.(6694-6696)Cac>Tac | p.H2232Y |
| HNSC | 14 | 20841840 | 20841840 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-A45Y-01A-11D-A25D-08 | TCGA-CV-A45Y-10A-01D-A25E-08 | g.chr14:20841840C>T | c.6601G>A | c.(6601-6603)Gca>Aca | p.A2201T |
| HNSC | 14 | 20845880 | 20845880 | + | Silent | SNP | G | G | A | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr14:20845880G>A | c.5754C>T | c.(5752-5754)ccC>ccT | p.P1918P |
| HNSC | 14 | 20845894 | 20845894 | + | Missense_Mutation | SNP | A | A | T | TCGA-CR-7389-01A-11D-2012-08 | TCGA-CR-7389-10A-01D-2013-08 | g.chr14:20845894A>T | c.5740T>A | c.(5740-5742)Tct>Act | p.S1914T |
| HNSC | 14 | 20846329 | 20846329 | + | Missense_Mutation | SNP | C | C | G | TCGA-BA-4078-01A-01D-1434-08 | TCGA-BA-4078-10A-01D-1434-08 | g.chr14:20846329C>G | c.5575G>C | c.(5575-5577)Gtg>Ctg | p.V1859L |
| HNSC | 14 | 20848553 | 20848553 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-F7-A623-01A-11D-A28R-08 | TCGA-F7-A623-10A-01D-A28U-08 | g.chr14:20848553G>C | c.4844C>G | c.(4843-4845)tCa>tGa | p.S1615* |
| HNSC | 14 | 20849089 | 20849089 | + | Splice_Site | SNP | C | C | T | TCGA-BA-5555-01A-01D-1512-08 | TCGA-BA-5555-10A-01D-1512-08 | g.chr14:20849089C>T | | c.e33+1 | |
| HNSC | 14 | 20849805 | 20849805 | + | Silent | SNP | G | G | A | TCGA-CR-7371-01A-11D-2012-08 | TCGA-CR-7371-10A-01D-2013-08 | g.chr14:20849805G>A | c.4465C>T | c.(4465-4467)Ctg>Ttg | p.L1489L |
| HNSC | 14 | 20852060 | 20852060 | + | Silent | SNP | G | G | A | TCGA-MZ-A5BI-01A-31D-A34J-08 | TCGA-MZ-A5BI-10C-01D-A34M-08 | g.chr14:20852060G>A | c.3552C>T | c.(3550-3552)gcC>gcT | p.A1184A |
| HNSC | 14 | 20852263 | 20852263 | + | Silent | SNP | C | C | T | TCGA-DQ-7588-01A-11D-2078-08 | TCGA-DQ-7588-10B-01D-2078-08 | g.chr14:20852263C>T | c.3468G>A | c.(3466-3468)ctG>ctA | p.L1156L |
| HNSC | 14 | 20854732 | 20854732 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-4737-01A-01D-1434-08 | TCGA-CN-4737-10A-01D-1434-08 | g.chr14:20854732C>T | c.2735G>A | c.(2734-2736)gGg>gAg | p.G912E |
| HNSC | 14 | 20856088 | 20856088 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-5442-01A-01D-1512-08 | TCGA-CV-5442-11A-01D-1512-08 | g.chr14:20856088G>T | c.2660C>A | c.(2659-2661)cCc>cAc | p.P887H |
| HNSC | 14 | 20858878 | 20858879 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr14:20858878_20858879insA | c.2295_2296insT | c.(2293-2298)tttgggfs | p.G766fs |
| HNSC | 14 | 20871907 | 20871907 | + | Missense_Mutation | SNP | T | T | A | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr14:20871907T>A | c.1169A>T | c.(1168-1170)cAc>cTc | p.H390L |
| HNSC | 14 | 20872897 | 20872897 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-A640-01A-21D-A30E-08 | TCGA-CN-A640-10A-01D-A30H-08 | g.chr14:20872897C>T | c.905G>A | c.(904-906)cGg>cAg | p.R302Q |
| HNSC | 14 | 20874441 | 20874441 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-A6K1-01A-11D-A31L-08 | TCGA-CV-A6K1-10A-01D-A31J-08 | g.chr14:20874441T>C | c.686A>G | c.(685-687)gAc>gGc | p.D229G |
| HNSC | 14 | 20874489 | 20874489 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7242-01A-11D-2012-08 | TCGA-CV-7242-10A-01D-2013-08 | g.chr14:20874489C>T | c.638G>A | c.(637-639)gGa>gAa | p.G213E |
| HNSC | 14 | 20876232 | 20876233 | + | Frame_Shift_Del | DEL | AC | AC | - | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr14:20876232_20876233delAC | c.366_367delGT | c.(364-369)gtgtctfs | p.S123fs |
| HNSC | 14 | 20876530 | 20876530 | + | Silent | SNP | A | A | G | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr14:20876530A>G | c.69T>C | c.(67-69)gcT>gcC | p.A23A |
| KICH | 14 | 20854663 | 20854663 | + | Missense_Mutation | SNP | C | C | A | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr14:20854663C>A | c.2804G>T | c.(2803-2805)aGc>aTc | p.S935I |
| KIPAN | 14 | 20839416 | 20839416 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-SX-A7SR-01A-12D-A35Z-10 | TCGA-SX-A7SR-10A-01D-A35Z-10 | g.chr14:20839416delA | c.7278delT | c.(7276-7278)tttfs | p.F2426fs |
| KIPAN | 14 | 20841196 | 20841196 | + | Missense_Mutation | SNP | C | C | T | TCGA-BQ-7060-01A-11D-1961-08 | TCGA-BQ-7060-11A-01D-1961-08 | g.chr14:20841196C>T | c.6925G>A | c.(6925-6927)Gaa>Aaa | p.E2309K |
| KIPAN | 14 | 20845481 | 20845481 | + | Silent | SNP | G | G | A | TCGA-BQ-7051-01A-12D-1961-08 | TCGA-BQ-7051-11A-02D-1961-08 | g.chr14:20845481G>A | c.6046C>T | c.(6046-6048)Cta>Tta | p.L2016L |
| KIPAN | 14 | 20845648 | 20845648 | + | Missense_Mutation | SNP | G | G | T | TCGA-HE-A5NF-01A-11D-A26P-10 | TCGA-HE-A5NF-10A-01D-A26P-10 | g.chr14:20845648G>T | c.5879C>A | c.(5878-5880)tCc>tAc | p.S1960Y |
| KIPAN | 14 | 20846267 | 20846267 | + | Silent | SNP | G | G | C | TCGA-A4-A57E-01A-11D-A26P-10 | TCGA-A4-A57E-10A-01D-A26P-10 | g.chr14:20846267G>C | c.5637C>G | c.(5635-5637)gcC>gcG | p.A1879A |
| KIPAN | 14 | 20846278 | 20846278 | + | Missense_Mutation | SNP | G | G | A | TCGA-2Z-A9J3-01A-12D-A382-10 | TCGA-2Z-A9J3-10A-01D-A385-10 | g.chr14:20846278G>A | c.5626C>T | c.(5626-5628)Cgg>Tgg | p.R1876W |
| KIPAN | 14 | 20847178 | 20847178 | + | Silent | SNP | G | G | A | TCGA-BP-5178-01A-01D-1429-08 | TCGA-BP-5178-11A-01D-1429-08 | g.chr14:20847178G>A | c.5214C>T | c.(5212-5214)gaC>gaT | p.D1738D |
| KIPAN | 14 | 20854663 | 20854663 | + | Missense_Mutation | SNP | C | C | A | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr14:20854663C>A | c.2804G>T | c.(2803-2805)aGc>aTc | p.S935I |
| KIPAN | 14 | 20857434 | 20857434 | + | Missense_Mutation | SNP | C | C | T | TCGA-A4-7286-01A-11D-2136-08 | TCGA-A4-7286-10A-01D-2136-08 | g.chr14:20857434C>T | c.2488G>A | c.(2488-2490)Gat>Aat | p.D830N |
| KIPAN | 14 | 20864842 | 20864842 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-4170-01A-02D-1366-10 | TCGA-BP-4170-11A-01D-1366-10 | g.chr14:20864842G>T | c.1597C>A | c.(1597-1599)Ctg>Atg | p.L533M |
| KIPAN | 14 | 20864870 | 20864870 | + | Missense_Mutation | SNP | G | G | T | TCGA-AK-3461-01A-02D-1361-10 | TCGA-AK-3461-10A-01D-1361-10 | g.chr14:20864870G>T | c.1569C>A | c.(1567-1569)ttC>ttA | p.F523L |
| KIRC | 14 | 20847178 | 20847178 | + | Silent | SNP | G | G | A | TCGA-BP-5178-01A-01D-1429-08 | TCGA-BP-5178-11A-01D-1429-08 | g.chr14:20847178G>A | c.5214C>T | c.(5212-5214)gaC>gaT | p.D1738D |
| KIRC | 14 | 20864842 | 20864842 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-4170-01A-02D-1366-10 | TCGA-BP-4170-11A-01D-1366-10 | g.chr14:20864842G>T | c.1597C>A | c.(1597-1599)Ctg>Atg | p.L533M |
| KIRC | 14 | 20864870 | 20864870 | + | Missense_Mutation | SNP | G | G | T | TCGA-AK-3461-01A-02D-1361-10 | TCGA-AK-3461-10A-01D-1361-10 | g.chr14:20864870G>T | c.1569C>A | c.(1567-1569)ttC>ttA | p.F523L |
| KIRP | 14 | 20839416 | 20839416 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-SX-A7SR-01A-12D-A35Z-10 | TCGA-SX-A7SR-10A-01D-A35Z-10 | g.chr14:20839416delA | c.7278delT | c.(7276-7278)tttfs | p.F2426fs |
| KIRP | 14 | 20841196 | 20841196 | + | Missense_Mutation | SNP | C | C | T | TCGA-BQ-7060-01A-11D-1961-08 | TCGA-BQ-7060-11A-01D-1961-08 | g.chr14:20841196C>T | c.6925G>A | c.(6925-6927)Gaa>Aaa | p.E2309K |
| KIRP | 14 | 20845481 | 20845481 | + | Silent | SNP | G | G | A | TCGA-BQ-7051-01A-12D-1961-08 | TCGA-BQ-7051-11A-02D-1961-08 | g.chr14:20845481G>A | c.6046C>T | c.(6046-6048)Cta>Tta | p.L2016L |
| KIRP | 14 | 20845648 | 20845648 | + | Missense_Mutation | SNP | G | G | T | TCGA-HE-A5NF-01A-11D-A26P-10 | TCGA-HE-A5NF-10A-01D-A26P-10 | g.chr14:20845648G>T | c.5879C>A | c.(5878-5880)tCc>tAc | p.S1960Y |
| KIRP | 14 | 20846267 | 20846267 | + | Silent | SNP | G | G | C | TCGA-A4-A57E-01A-11D-A26P-10 | TCGA-A4-A57E-10A-01D-A26P-10 | g.chr14:20846267G>C | c.5637C>G | c.(5635-5637)gcC>gcG | p.A1879A |
| KIRP | 14 | 20846278 | 20846278 | + | Missense_Mutation | SNP | G | G | A | TCGA-2Z-A9J3-01A-12D-A382-10 | TCGA-2Z-A9J3-10A-01D-A385-10 | g.chr14:20846278G>A | c.5626C>T | c.(5626-5628)Cgg>Tgg | p.R1876W |
| KIRP | 14 | 20857434 | 20857434 | + | Missense_Mutation | SNP | C | C | T | TCGA-A4-7286-01A-11D-2136-08 | TCGA-A4-7286-10A-01D-2136-08 | g.chr14:20857434C>T | c.2488G>A | c.(2488-2490)Gat>Aat | p.D830N |
| LGG | 14 | 20845586 | 20845586 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20845586T>C | c.5941A>G | c.(5941-5943)Aag>Gag | p.K1981E |
| LGG | 14 | 20845812 | 20845812 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20845812C>T | c.5822G>A | c.(5821-5823)cGg>cAg | p.R1941Q |
| LGG | 14 | 20846220 | 20846220 | + | Missense_Mutation | SNP | G | G | A | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr14:20846220G>A | c.5684C>T | c.(5683-5685)gCg>gTg | p.A1895V |
| LGG | 14 | 20850092 | 20850092 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20850092G>A | c.4404C>T | c.(4402-4404)tgC>tgT | p.C1468C |
| LGG | 14 | 20851712 | 20851712 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20851712C>T | c.3802G>A | c.(3802-3804)Gct>Act | p.A1268T |
| LGG | 14 | 20852291 | 20852291 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20852291C>T | c.3440G>A | c.(3439-3441)cGc>cAc | p.R1147H |
| LGG | 14 | 20852762 | 20852762 | + | Missense_Mutation | SNP | C | C | T | TCGA-TM-A7C4-01A-11D-A32B-08 | TCGA-TM-A7C4-10A-01D-A329-08 | g.chr14:20852762C>T | c.3218G>A | c.(3217-3219)cGc>cAc | p.R1073H |
| LGG | 14 | 20854314 | 20854314 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20854314G>A | c.2902C>T | c.(2902-2904)Ctg>Ttg | p.L968L |
| LGG | 14 | 20854643 | 20854643 | + | Missense_Mutation | SNP | G | G | A | TCGA-P5-A5EZ-01A-11D-A27K-08 | TCGA-P5-A5EZ-10A-01D-A27N-08 | g.chr14:20854643G>A | c.2824C>T | c.(2824-2826)Cgc>Tgc | p.R942C |
| LGG | 14 | 20871901 | 20871901 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:20871901C>T | c.1175G>A | c.(1174-1176)cGc>cAc | p.R392H |
| LIHC | 14 | 20840992 | 20840992 | + | Missense_Mutation | SNP | T | T | C | TCGA-BC-A3KF-01A-11D-A20W-10 | TCGA-BC-A3KF-10A-01D-A20W-10 | g.chr14:20840992T>C | c.6976A>G | c.(6976-6978)Atc>Gtc | p.I2326V |
| LIHC | 14 | 20841220 | 20841226 | + | Frame_Shift_Del | DEL | CTTGATT | CTTGATT | - | TCGA-2Y-A9GZ-01A-11D-A38X-10 | TCGA-2Y-A9GZ-10A-01D-A38X-10 | g.chr14:20841220_20841226delCTTGATT | c.6895_6901delAATCAAG | c.(6895-6903)aatcaagctfs | p.NQA2299fs |
| LIHC | 14 | 20846338 | 20846338 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr14:20846338delC | c.5566delG | c.(5566-5568)gttfs | p.V1857fs |
| LIHC | 14 | 20847004 | 20847004 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AADA-01A-11D-A40R-10 | TCGA-DD-AADA-10A-01D-A40U-10 | g.chr14:20847004T>C | c.5261A>G | c.(5260-5262)cAg>cGg | p.Q1754R |
| LIHC | 14 | 20848600 | 20848600 | + | Silent | SNP | G | G | T | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr14:20848600G>T | c.4797C>A | c.(4795-4797)ccC>ccA | p.P1599P |
| LIHC | 14 | 20850191 | 20850191 | + | Silent | SNP | C | C | T | TCGA-CC-A8HS-01A-11D-A35Z-10 | TCGA-CC-A8HS-10A-01D-A35Z-10 | g.chr14:20850191C>T | c.4305G>A | c.(4303-4305)ctG>ctA | p.L1435L |
| LIHC | 14 | 20851687 | 20851687 | + | Missense_Mutation | SNP | C | C | A | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr14:20851687C>A | c.3827G>T | c.(3826-3828)gGg>gTg | p.G1276V |
| LIHC | 14 | 20851711 | 20851711 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-DD-AACJ-01A-11D-A40R-10 | TCGA-DD-AACJ-10A-01D-A40U-10 | g.chr14:20851711delG | c.3803delC | c.(3802-3804)gctfs | p.A1268fs |
| LIHC | 14 | 20852626 | 20852626 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AAE1-01A-11D-A40R-10 | TCGA-DD-AAE1-10A-01D-A40U-10 | g.chr14:20852626T>C | c.3263A>G | c.(3262-3264)tAt>tGt | p.Y1088C |
| LIHC | 14 | 20853228 | 20853228 | + | Missense_Mutation | SNP | T | T | C | TCGA-G3-A3CG-01A-11D-A20W-10 | TCGA-G3-A3CG-10A-01D-A20W-10 | g.chr14:20853228T>C | c.3023A>G | c.(3022-3024)gAg>gGg | p.E1008G |
| LIHC | 14 | 20859791 | 20859791 | + | Silent | SNP | T | T | C | TCGA-CC-A3MA-01A-11D-A20W-10 | TCGA-CC-A3MA-10A-01D-A20W-10 | g.chr14:20859791T>C | c.2064A>G | c.(2062-2064)gcA>gcG | p.A688A |
| LIHC | 14 | 20871535 | 20871535 | + | Splice_Site | SNP | C | C | A | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr14:20871535C>A | | c.e7+1 | |
| LIHC | 14 | 20872028 | 20872028 | + | Missense_Mutation | SNP | C | C | A | TCGA-DD-A116-01A-11D-A12Z-10 | TCGA-DD-A116-10A-01D-A12Z-10 | g.chr14:20872028C>A | c.1048G>T | c.(1048-1050)Gat>Tat | p.D350Y |
| LIHC | 14 | 20872802 | 20872802 | + | Missense_Mutation | SNP | A | A | G | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr14:20872802A>G | c.1000T>C | c.(1000-1002)Tct>Cct | p.S334P |
| LIHC | 14 | 20874483 | 20874483 | + | Missense_Mutation | SNP | T | T | C | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr14:20874483T>C | c.644A>G | c.(643-645)gAg>gGg | p.E215G |
| LIHC | 14 | 20876328 | 20876328 | + | Missense_Mutation | SNP | T | T | G | TCGA-G3-A6UC-01A-21D-A33K-10 | TCGA-G3-A6UC-10A-01D-A33K-10 | g.chr14:20876328T>G | c.271A>C | c.(271-273)Atg>Ctg | p.M91L |
| LIHC | 14 | 20876563 | 20876563 | + | Silent | SNP | T | T | A | TCGA-DD-AAE3-01A-11D-A40R-10 | TCGA-DD-AAE3-10A-01D-A40U-10 | g.chr14:20876563T>A | c.36A>T | c.(34-36)ccA>ccT | p.P12P |
| LUAD | 14 | 20837502 | 20837502 | + | Splice_Site | SNP | C | C | A | TCGA-55-8302-01A-11D-2323-08 | TCGA-55-8302-10A-01D-2323-08 | g.chr14:20837502C>A | | c.e53+1 | |
| LUAD | 14 | 20837598 | 20837598 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z021-01A-01W-0746-08 | TCGA-17-Z021-11A-01W-0746-08 | g.chr14:20837598G>C | c.7561C>G | c.(7561-7563)Cca>Gca | p.P2521A |
| LUAD | 14 | 20837665 | 20837665 | + | Silent | SNP | T | T | C | TCGA-17-Z045-01A-01W-0746-08 | TCGA-17-Z045-11A-01W-0747-08 | g.chr14:20837665T>C | c.7494A>G | c.(7492-7494)gaA>gaG | p.E2498E |
| LUAD | 14 | 20841524 | 20841524 | + | Missense_Mutation | SNP | G | G | C | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr14:20841524G>C | c.6719C>G | c.(6718-6720)cCa>cGa | p.P2240R |
| LUAD | 14 | 20841837 | 20841837 | + | Splice_Site | SNP | C | C | A | TCGA-91-6848-01A-11D-1945-08 | TCGA-91-6848-11A-01D-1945-08 | g.chr14:20841837C>A | c.6604G>T | c.(6604-6606)Gct>Tct | p.A2202S |
| LUAD | 14 | 20841881 | 20841881 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr14:20841881G>C | c.6560C>G | c.(6559-6561)tCa>tGa | p.S2187* |
| LUAD | 14 | 20843947 | 20843947 | + | Silent | SNP | G | G | A | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr14:20843947G>A | c.6330C>T | c.(6328-6330)gtC>gtT | p.V2110V |
| LUAD | 14 | 20845891 | 20845891 | + | Silent | SNP | G | G | A | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr14:20845891G>A | c.5743C>T | c.(5743-5745)Ctg>Ttg | p.L1915L |
| LUAD | 14 | 20845902 | 20845902 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr14:20845902C>A | c.5732G>T | c.(5731-5733)tGg>tTg | p.W1911L |
| LUAD | 14 | 20845913 | 20845913 | + | Splice_Site | SNP | C | C | A | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr14:20845913C>A | | c.e40-1 | |
| LUAD | 14 | 20847204 | 20847204 | + | Missense_Mutation | SNP | C | C | T | TCGA-78-8662-01A-11D-2393-08 | TCGA-78-8662-10A-01D-2393-08 | g.chr14:20847204C>T | c.5188G>A | c.(5188-5190)Gat>Aat | p.D1730N |
| LUAD | 14 | 20848504 | 20848504 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-7978-01A-11D-2184-08 | TCGA-69-7978-10A-01D-2184-08 | g.chr14:20848504C>A | c.4893G>T | c.(4891-4893)caG>caT | p.Q1631H |
| LUAD | 14 | 20849099 | 20849099 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr14:20849099C>T | c.4753G>A | c.(4753-4755)Gcc>Acc | p.A1585T |
| LUAD | 14 | 20849471 | 20849471 | + | Splice_Site | SNP | C | C | A | TCGA-64-1679-01A-21D-2063-08 | TCGA-64-1679-10A-01D-2063-08 | g.chr14:20849471C>A | | c.e32+1 | |
| LUAD | 14 | 20849739 | 20849739 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr14:20849739C>A | c.4531G>T | c.(4531-4533)Gag>Tag | p.E1511* |
| LUAD | 14 | 20849819 | 20849819 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-7659-01A-11D-2063-08 | TCGA-44-7659-10A-01D-2063-08 | g.chr14:20849819C>A | c.4451G>T | c.(4450-4452)cGc>cTc | p.R1484L |
| LUAD | 14 | 20849833 | 20849833 | + | Missense_Mutation | SNP | C | C | A | TCGA-97-7937-01A-11D-2167-08 | TCGA-97-7937-10A-01D-2167-08 | g.chr14:20849833C>A | c.4437G>T | c.(4435-4437)gaG>gaT | p.E1479D |
| LUAD | 14 | 20850171 | 20850171 | + | Missense_Mutation | SNP | G | G | A | TCGA-62-8395-01A-11D-2323-08 | TCGA-62-8395-10A-01D-2323-08 | g.chr14:20850171G>A | c.4325C>T | c.(4324-4326)cCg>cTg | p.P1442L |
| LUAD | 14 | 20850472 | 20850472 | + | Missense_Mutation | SNP | A | A | T | TCGA-17-Z057-01A-01W-0747-08 | TCGA-17-Z057-11A-01W-0747-08 | g.chr14:20850472A>T | c.4184T>A | c.(4183-4185)cTg>cAg | p.L1395Q |
| LUAD | 14 | 20850850 | 20850850 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-05-4250-01A-01D-1105-08 | TCGA-05-4250-10A-01D-1105-08 | g.chr14:20850850C>A | c.4072G>T | c.(4072-4074)Gaa>Taa | p.E1358* |
| LUAD | 14 | 20851369 | 20851369 | + | Silent | SNP | G | G | A | TCGA-97-A4M0-01A-11D-A24P-08 | TCGA-97-A4M0-10A-01D-A24P-08 | g.chr14:20851369G>A | c.4011C>T | c.(4009-4011)taC>taT | p.Y1337Y |
| LUAD | 14 | 20851649 | 20851649 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-44-A47A-01A-21D-A24D-08 | TCGA-44-A47A-10A-01D-A24F-08 | g.chr14:20851649delG | c.3865delC | c.(3865-3867)cggfs | p.R1289fs |
| LUAD | 14 | 20851722 | 20851722 | + | Silent | SNP | G | G | T | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr14:20851722G>T | c.3792C>A | c.(3790-3792)atC>atA | p.I1264I |
| LUAD | 14 | 20852618 | 20852618 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4432-01A-01D-1265-08 | TCGA-05-4432-10A-01D-1265-08 | g.chr14:20852618C>A | c.3271G>T | c.(3271-3273)Ggg>Tgg | p.G1091W |
| LUAD | 14 | 20852648 | 20852648 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr14:20852648C>T | c.3241G>A | c.(3241-3243)Ggt>Agt | p.G1081S |
| LUAD | 14 | 20854332 | 20854332 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-55-6642-01A-11D-1855-08 | TCGA-55-6642-11A-01D-1855-08 | g.chr14:20854332C>A | c.2884G>T | c.(2884-2886)Gag>Tag | p.E962* |
| LUAD | 14 | 20856064 | 20856064 | + | Splice_Site | SNP | C | C | A | TCGA-50-5049-01A-01D-1625-08 | TCGA-50-5049-10A-01D-1625-08 | g.chr14:20856064C>A | c.2684G>T | c.(2683-2685)gGa>gTa | p.G895V |
| LUAD | 14 | 20856104 | 20856104 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr14:20856104C>A | c.2644G>T | c.(2644-2646)Gag>Tag | p.E882* |
| LUAD | 14 | 20857777 | 20857777 | + | Silent | SNP | T | T | A | TCGA-73-4659-01A-01D-1265-08 | TCGA-73-4659-11A-01D-1265-08 | g.chr14:20857777T>A | c.2457A>T | c.(2455-2457)gtA>gtT | p.V819V |
| LUAD | 14 | 20859155 | 20859155 | + | Missense_Mutation | SNP | A | A | C | TCGA-17-Z058-01A-01W-0747-08 | TCGA-17-Z058-11A-01W-0747-08 | g.chr14:20859155A>C | c.2198T>G | c.(2197-2199)gTg>gGg | p.V733G |
| LUAD | 14 | 20859156 | 20859156 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-7159-01A-11D-2036-08 | TCGA-78-7159-10A-01D-2036-08 | g.chr14:20859156C>A | c.2197G>T | c.(2197-2199)Gtg>Ttg | p.V733L |
| LUAD | 14 | 20859842 | 20859842 | + | Silent | SNP | C | C | A | TCGA-86-8054-01A-11D-2238-08 | TCGA-86-8054-10A-01D-2238-08 | g.chr14:20859842C>A | c.2013G>T | c.(2011-2013)ctG>ctT | p.L671L |
| LUAD | 14 | 20859894 | 20859894 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-1592-01A-01D-0969-08 | TCGA-55-1592-11A-01D-0969-08 | g.chr14:20859894C>G | c.1961G>C | c.(1960-1962)aGg>aCg | p.R654T |
| LUAD | 14 | 20859920 | 20859920 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-38-4629-01A-02D-1265-08 | TCGA-38-4629-11A-01D-1265-08 | g.chr14:20859920C>T | c.1935G>A | c.(1933-1935)tgG>tgA | p.W645* |
| LUAD | 14 | 20864037 | 20864037 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8281-01A-11D-2284-08 | TCGA-86-8281-10A-01D-2284-08 | g.chr14:20864037C>A | c.1731G>T | c.(1729-1731)gaG>gaT | p.E577D |
| LUAD | 14 | 20864787 | 20864787 | + | Missense_Mutation | SNP | T | T | A | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr14:20864787T>A | c.1652A>T | c.(1651-1653)cAg>cTg | p.Q551L |
| LUAD | 14 | 20864809 | 20864809 | + | Missense_Mutation | SNP | C | C | T | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr14:20864809C>T | c.1630G>A | c.(1630-1632)Gag>Aag | p.E544K |
| LUAD | 14 | 20864835 | 20864835 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-5779-01A-01D-1625-08 | TCGA-64-5779-10A-01D-1625-08 | g.chr14:20864835C>A | c.1604G>T | c.(1603-1605)cGg>cTg | p.R535L |
| LUAD | 14 | 20864840 | 20864840 | + | Silent | SNP | C | C | G | TCGA-91-6848-01A-11D-1945-08 | TCGA-91-6848-11A-01D-1945-08 | g.chr14:20864840C>G | c.1599G>C | c.(1597-1599)ctG>ctC | p.L533L |
| LUAD | 14 | 20869741 | 20869741 | + | Splice_Site | SNP | C | C | A | TCGA-55-8616-01A-11D-2393-08 | TCGA-55-8616-10A-01D-2393-08 | g.chr14:20869741C>A | | c.e8-1 | |
| LUAD | 14 | 20871902 | 20871902 | + | Missense_Mutation | SNP | G | G | A | TCGA-50-6594-01A-11D-1753-08 | TCGA-50-6594-11A-01D-1753-08 | g.chr14:20871902G>A | c.1174C>T | c.(1174-1176)Cgc>Tgc | p.R392C |
| LUAD | 14 | 20872001 | 20872001 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr14:20872001C>A | c.1075G>T | c.(1075-1077)Gcc>Tcc | p.A359S |
| LUAD | 14 | 20872851 | 20872851 | + | Silent | SNP | C | C | T | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr14:20872851C>T | c.951G>A | c.(949-951)gcG>gcA | p.A317A |
| LUAD | 14 | 20873650 | 20873650 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8302-01A-11D-2323-08 | TCGA-55-8302-10A-01D-2323-08 | g.chr14:20873650C>A | c.830G>T | c.(829-831)tGt>tTt | p.C277F |
| LUAD | 14 | 20876106 | 20876106 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-38-4631-01A-01D-1753-08 | TCGA-38-4631-11A-01D-1753-08 | g.chr14:20876106C>A | c.493G>T | c.(493-495)Gga>Tga | p.G165* |
| LUAD | 14 | 20876171 | 20876171 | + | Missense_Mutation | SNP | C | C | T | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr14:20876171C>T | c.428G>A | c.(427-429)cGt>cAt | p.R143H |
| LUAD | 14 | 20876303 | 20876303 | + | Missense_Mutation | SNP | G | G | C | TCGA-97-7941-01A-11D-2184-08 | TCGA-97-7941-10A-01D-2184-08 | g.chr14:20876303G>C | c.296C>G | c.(295-297)tCt>tGt | p.S99C |
| LUAD | 14 | 20876539 | 20876539 | + | Silent | SNP | C | C | A | TCGA-55-A4DG-01A-11D-A24D-08 | TCGA-55-A4DG-10A-01D-A24F-08 | g.chr14:20876539C>A | c.60G>T | c.(58-60)cgG>cgT | p.R20R |
| LUAD | 14 | 20876563 | 20876563 | + | Silent | SNP | T | T | A | TCGA-69-7974-01A-11D-2184-08 | TCGA-69-7974-10A-01D-2184-08 | g.chr14:20876563T>A | c.36A>T | c.(34-36)ccA>ccT | p.P12P |
| LUSC | 14 | 20837529 | 20837529 | + | Missense_Mutation | SNP | G | G | A | TCGA-60-2723-01A-01D-1522-08 | TCGA-60-2723-11A-01D-1522-08 | g.chr14:20837529G>A | c.7630C>T | c.(7630-7632)Cat>Tat | p.H2544Y |
| LUSC | 14 | 20845477 | 20845477 | + | Missense_Mutation | SNP | C | C | T | TCGA-33-4566-01A-01D-1441-08 | TCGA-33-4566-11A-01D-1441-08 | g.chr14:20845477C>T | c.6050G>A | c.(6049-6051)gGa>gAa | p.G2017E |
| LUSC | 14 | 20848129 | 20848130 | + | Missense_Mutation | DNP | GC | GC | TA | TCGA-46-6025-01A-11D-1817-08 | TCGA-46-6025-10A-01D-1817-08 | g.chr14:20848129_20848130GC>TA | c.5086_5087GC>TA | c.(5086-5088)GCc>TAc | p.A1696Y |
| LUSC | 14 | 20849731 | 20849731 | + | Silent | SNP | C | C | A | TCGA-46-6026-01A-11D-1817-08 | TCGA-46-6026-10A-01D-1817-08 | g.chr14:20849731C>A | c.4539G>T | c.(4537-4539)acG>acT | p.T1513T |
| LUSC | 14 | 20852761 | 20852761 | + | Silent | SNP | G | G | T | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr14:20852761G>T | c.3219C>A | c.(3217-3219)cgC>cgA | p.R1073R |
| LUSC | 14 | 20854783 | 20854783 | + | Splice_Site | SNP | C | C | G | TCGA-33-4533-01A-01D-1267-08 | TCGA-33-4533-11A-01D-1267-08 | g.chr14:20854783C>G | | c.e19-1 | |
| LUSC | 14 | 20857439 | 20857439 | + | Missense_Mutation | SNP | G | G | T | TCGA-18-3406-01A-01D-0983-08 | TCGA-18-3406-11A-01D-0983-08 | g.chr14:20857439G>T | c.2483C>A | c.(2482-2484)cCc>cAc | p.P828H |
| LUSC | 14 | 20864797 | 20864797 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr14:20864797G>A | c.1642C>T | c.(1642-1644)Cag>Tag | p.Q548* |
| LUSC | 14 | 20864868 | 20864868 | + | Missense_Mutation | SNP | A | A | T | TCGA-66-2758-01A-02D-1522-08 | TCGA-66-2758-11A-01D-1522-08 | g.chr14:20864868A>T | c.1571T>A | c.(1570-1572)aTg>aAg | p.M524K |
| OV | 14 | 20836605 | 20836605 | + | Silent | SNP | A | A | G | TCGA-13-1492-01A-01D-0472-08 | TCGA-13-1492-10A-01W-0545-08 | g.chr14:20836605A>G | c.7875T>C | c.(7873-7875)aaT>aaC | p.N2625N |
| OV | 14 | 20841695 | 20841695 | + | Missense_Mutation | SNP | C | C | T | TCGA-13-2059-01A-01D-1526-09 | TCGA-13-2059-10A-01D-1526-09 | g.chr14:20841695C>T | c.6652G>A | c.(6652-6654)Ggg>Agg | p.G2218R |
| OV | 14 | 20844277 | 20844277 | + | Missense_Mutation | SNP | C | C | T | TCGA-23-2643-01A-01D-1526-09 | TCGA-23-2643-10A-01D-1526-09 | g.chr14:20844277C>T | c.6235G>A | c.(6235-6237)Ggg>Agg | p.G2079R |
| OV | 14 | 20846616 | 20846616 | + | Missense_Mutation | SNP | C | C | G | TCGA-25-2392-01A-01W-0799-08 | TCGA-25-2392-10A-01W-0799-08 | g.chr14:20846616C>G | c.5431G>C | c.(5431-5433)Gag>Cag | p.E1811Q |
| OV | 14 | 20847231 | 20847231 | + | Missense_Mutation | SNP | T | T | C | TCGA-61-1904-01A-01W-0639-09 | TCGA-61-1904-11A-01W-0640-09 | g.chr14:20847231T>C | c.5161A>G | c.(5161-5163)Atc>Gtc | p.I1721V |
| OV | 14 | 20851397 | 20851397 | + | Missense_Mutation | SNP | C | C | T | TCGA-30-1714-01A-02W-0633-09 | TCGA-30-1714-10A-01W-0633-09 | g.chr14:20851397C>T | c.3983G>A | c.(3982-3984)cGg>cAg | p.R1328Q |
| OV | 14 | 20851455 | 20851455 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-24-1604-01A-01W-0552-10 | TCGA-24-1604-10A-01W-0552-10 | g.chr14:20851455G>A | c.3925C>T | c.(3925-3927)Cag>Tag | p.Q1309* |
| OV | 14 | 20851795 | 20851795 | + | Missense_Mutation | SNP | A | A | G | TCGA-13-0801-01A-01W-0370-10 | TCGA-13-0801-10A-01W-0370-10 | g.chr14:20851795A>G | c.3719T>C | c.(3718-3720)gTg>gCg | p.V1240A |
| OV | 14 | 20864064 | 20864064 | + | Silent | SNP | G | G | A | TCGA-61-2110-01A-01W-0722-08 | TCGA-61-2110-11A-01W-0723-08 | g.chr14:20864064G>A | c.1704C>T | c.(1702-1704)aaC>aaT | p.N568N |
| OV | 14 | 20869265 | 20869265 | + | Missense_Mutation | SNP | C | C | T | TCGA-61-1919-01A-01W-0699-08 | TCGA-61-1919-11A-01W-0700-08 | g.chr14:20869265C>T | c.1427G>A | c.(1426-1428)cGc>cAc | p.R476H |
| OV | 14 | 20876541 | 20876541 | + | Missense_Mutation | SNP | G | G | A | TCGA-13-2057-01A-02D-1526-09 | TCGA-13-2057-10A-01D-1526-09 | g.chr14:20876541G>A | c.58C>T | c.(58-60)Cgg>Tgg | p.R20W |
| PAAD | 14 | 20841221 | 20841221 | + | Silent | SNP | T | T | C | TCGA-IB-A7LX-01A-12D-A36O-08 | TCGA-IB-A7LX-10A-01D-A367-08 | g.chr14:20841221T>C | c.6900A>G | c.(6898-6900)caA>caG | p.Q2300Q |
| PAAD | 14 | 20841224 | 20841224 | + | Silent | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:20841224A>G | c.6897T>C | c.(6895-6897)aaT>aaC | p.N2299N |
| PAAD | 14 | 20841276 | 20841276 | + | Missense_Mutation | SNP | G | G | A | TCGA-HZ-A77O-01A-11D-A33T-08 | TCGA-HZ-A77O-10A-01D-A33W-08 | g.chr14:20841276G>A | c.6845C>T | c.(6844-6846)gCc>gTc | p.A2282V |
| PAAD | 14 | 20841685 | 20841685 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:20841685C>T | c.6662G>A | c.(6661-6663)cGg>cAg | p.R2221Q |
| PAAD | 14 | 20841723 | 20841723 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:20841723C>T | c.6624G>A | c.(6622-6624)gaG>gaA | p.E2208E |
| PAAD | 14 | 20843925 | 20843925 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:20843925C>T | c.6352G>A | c.(6352-6354)Gat>Aat | p.D2118N |
| PAAD | 14 | 20850180 | 20850180 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:20850180C>T | c.4316G>A | c.(4315-4317)cGg>cAg | p.R1439Q |
| PAAD | 14 | 20851408 | 20851408 | + | Silent | SNP | A | A | C | TCGA-HZ-8637-01A-11D-2396-08 | TCGA-HZ-8637-10A-01D-2396-08 | g.chr14:20851408A>C | c.3972T>G | c.(3970-3972)tcT>tcG | p.S1324S |
| PAAD | 14 | 20852647 | 20852647 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-IB-A5SS-01A-11D-A32N-08 | TCGA-IB-A5SS-10A-01D-A32N-08 | g.chr14:20852647delC | c.3242delG | c.(3241-3243)ggtfs | p.G1081fs |
| PAAD | 14 | 20852647 | 20852647 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-IB-A6UF-01A-23D-A33T-08 | TCGA-IB-A6UF-10A-01D-A33W-08 | g.chr14:20852647delC | c.3242delG | c.(3241-3243)ggtfs | p.G1081fs |
| PAAD | 14 | 20852647 | 20852647 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-US-A77J-01A-11D-A32N-08 | TCGA-US-A77J-11A-11D-A32N-08 | g.chr14:20852647delC | c.3242delG | c.(3241-3243)ggtfs | p.G1081fs |
| PAAD | 14 | 20854270 | 20854270 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-OE-A75W-01A-12D-A32N-08 | TCGA-OE-A75W-10A-01D-A32N-08 | g.chr14:20854270delG | c.2946delC | c.(2944-2946)cccfs | p.P982fs |
| PAAD | 14 | 20858856 | 20858856 | + | Missense_Mutation | SNP | G | G | A | TCGA-3A-A9IX-01A-11D-A40W-08 | TCGA-3A-A9IX-10A-01D-A40W-08 | g.chr14:20858856G>A | c.2318C>T | c.(2317-2319)gCt>gTt | p.A773V |
| PAAD | 14 | 20869179 | 20869179 | + | Missense_Mutation | SNP | G | G | A | TCGA-2L-AAQL-01A-11D-A38G-08 | TCGA-2L-AAQL-11A-11D-A38J-08 | g.chr14:20869179G>A | c.1513C>T | c.(1513-1515)Cgg>Tgg | p.R505W |
| PAAD | 14 | 20872901 | 20872901 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:20872901C>T | c.901G>A | c.(901-903)Gtc>Atc | p.V301I |
| PAAD | 14 | 20874475 | 20874477 | + | In_Frame_Del | DEL | CCT | CCT | - | TCGA-3A-A9IR-01A-11D-A38G-08 | TCGA-3A-A9IR-10A-01D-A38J-08 | g.chr14:20874475_20874477delCCT | c.650_652delAGG | c.(649-654)gaggtg>gtg | p.E217del |
| PCPG | 14 | 20837625 | 20837625 | + | Missense_Mutation | SNP | G | G | A | TCGA-QR-A70A-01A-11D-A35D-08 | TCGA-QR-A70A-10A-01D-A35B-08 | g.chr14:20837625G>A | c.7534C>T | c.(7534-7536)Cca>Tca | p.P2512S |
| PRAD | 14 | 20845843 | 20845843 | + | Missense_Mutation | SNP | G | G | A | TCGA-HC-7233-01A-11D-2114-08 | TCGA-HC-7233-10A-01D-2115-08 | g.chr14:20845843G>A | c.5791C>T | c.(5791-5793)Ctc>Ttc | p.L1931F |
| PRAD | 14 | 20846220 | 20846220 | + | Missense_Mutation | SNP | G | G | A | TCGA-CH-5794-01A-11D-1576-08 | TCGA-CH-5794-10A-01D-1577-08 | g.chr14:20846220G>A | c.5684C>T | c.(5683-5685)gCg>gTg | p.A1895V |
| PRAD | 14 | 20847208 | 20847208 | + | Silent | SNP | G | G | A | TCGA-HC-A9TE-01A-11D-A41K-08 | TCGA-HC-A9TE-10A-01D-A41N-08 | g.chr14:20847208G>A | c.5184C>T | c.(5182-5184)tcC>tcT | p.S1728S |
| PRAD | 14 | 20856080 | 20856080 | + | Missense_Mutation | SNP | G | G | A | TCGA-HC-7820-01A-11D-2114-08 | TCGA-HC-7820-10A-01D-2115-08 | g.chr14:20856080G>A | c.2668C>T | c.(2668-2670)Cct>Tct | p.P890S |
| PRAD | 14 | 20871916 | 20871916 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr14:20871916G>A | c.1160C>T | c.(1159-1161)gCc>gTc | p.A387V |
| PRAD | 14 | 20871919 | 20871919 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr14:20871919C>T | c.1157G>A | c.(1156-1158)cGg>cAg | p.R386Q |
| READ | 14 | 20857405 | 20857405 | + | Silent | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr14:20857405C>T | c.2517G>A | c.(2515-2517)gcG>gcA | p.A839A |
| READ | 14 | 20859205 | 20859205 | + | Silent | SNP | C | C | T | TCGA-CL-5917-01A-11D-1657-10 | TCGA-CL-5917-10A-01D-1657-10 | g.chr14:20859205C>T | c.2148G>A | c.(2146-2148)gcG>gcA | p.A716A |
| SARC | 14 | 20848393 | 20848393 | + | Splice_Site | SNP | C | C | G | TCGA-X6-A8C4-01A-11D-A36J-09 | TCGA-X6-A8C4-10A-01D-A36M-09 | g.chr14:20848393C>G | | c.e34+1 | |
| SARC | 14 | 20848597 | 20848597 | + | Silent | SNP | C | C | T | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr14:20848597C>T | c.4800G>A | c.(4798-4800)gaG>gaA | p.E1600E |
| SARC | 14 | 20876097 | 20876097 | + | Missense_Mutation | SNP | G | G | C | TCGA-PC-A5DL-01A-11D-A26G-09 | TCGA-PC-A5DL-10A-01D-A26G-09 | g.chr14:20876097G>C | c.502C>G | c.(502-504)Ctt>Gtt | p.L168V |
| SKCM | 14 | 20840970 | 20840970 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr14:20840970A>T | c.6998T>A | c.(6997-6999)tTt>tAt | p.F2333Y |
| SKCM | 14 | 20841843 | 20841843 | + | Missense_Mutation | SNP | G | G | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr14:20841843G>T | c.6598C>A | c.(6598-6600)Cgt>Agt | p.R2200S |
| SKCM | 14 | 20842691 | 20842691 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A4FD-06A-11D-A25O-08 | TCGA-FS-A4FD-10B-01D-A25O-08 | g.chr14:20842691G>A | c.6368C>T | c.(6367-6369)tCc>tTc | p.S2123F |
| SKCM | 14 | 20845516 | 20845516 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr14:20845516G>A | c.6011C>T | c.(6010-6012)tCc>tTc | p.S2004F |
| SKCM | 14 | 20845562 | 20845562 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3TV-06A-11D-A23B-08 | TCGA-FW-A3TV-10A-01D-A23B-08 | g.chr14:20845562C>T | c.5965G>A | c.(5965-5967)Gat>Aat | p.D1989N |
| SKCM | 14 | 20845648 | 20845648 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr14:20845648G>A | c.5879C>T | c.(5878-5880)tCc>tTc | p.S1960F |
| SKCM | 14 | 20845893 | 20845893 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2JK-06A-11D-A196-08 | TCGA-D3-A2JK-10A-01D-A198-08 | g.chr14:20845893G>A | c.5741C>T | c.(5740-5742)tCt>tTt | p.S1914F |
| SKCM | 14 | 20846357 | 20846357 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:20846357G>A | c.5547C>T | c.(5545-5547)gcC>gcT | p.A1849A |
| SKCM | 14 | 20846375 | 20846375 | + | Silent | SNP | G | G | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr14:20846375G>A | c.5529C>T | c.(5527-5529)gcC>gcT | p.A1843A |
| SKCM | 14 | 20846376 | 20846376 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr14:20846376G>A | c.5528C>T | c.(5527-5529)gCc>gTc | p.A1843V |
| SKCM | 14 | 20846559 | 20846559 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr14:20846559C>T | c.5488G>A | c.(5488-5490)Gat>Aat | p.D1830N |
| SKCM | 14 | 20846647 | 20846647 | + | Silent | SNP | G | G | A | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr14:20846647G>A | c.5400C>T | c.(5398-5400)ccC>ccT | p.P1800P |
| SKCM | 14 | 20848177 | 20848177 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr14:20848177G>A | c.5039C>T | c.(5038-5040)aCt>aTt | p.T1680I |
| SKCM | 14 | 20848394 | 20848394 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr14:20848394C>T | c.5003G>A | c.(5002-5004)aGc>aAc | p.S1668N |
| SKCM | 14 | 20848472 | 20848472 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:20848472G>A | c.4925C>T | c.(4924-4926)tCg>tTg | p.S1642L |
| SKCM | 14 | 20848535 | 20848535 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J3-06A-11D-A20D-08 | TCGA-EE-A3J3-10A-01D-A20D-08 | g.chr14:20848535G>A | c.4862C>T | c.(4861-4863)cCc>cTc | p.P1621L |
| SKCM | 14 | 20848538 | 20848538 | + | Missense_Mutation | SNP | T | T | C | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr14:20848538T>C | c.4859A>G | c.(4858-4860)tAc>tGc | p.Y1620C |
| SKCM | 14 | 20848605 | 20848605 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JI-06A-11D-A21A-08 | TCGA-EE-A3JI-10A-01D-A21A-08 | g.chr14:20848605G>A | c.4792C>T | c.(4792-4794)Ctc>Ttc | p.L1598F |
| SKCM | 14 | 20849134 | 20849134 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr14:20849134T>C | c.4718A>G | c.(4717-4719)gAa>gGa | p.E1573G |
| SKCM | 14 | 20849176 | 20849176 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51E-06A-11D-A25O-08 | TCGA-D3-A51E-10A-01D-A25O-08 | g.chr14:20849176G>A | c.4676C>T | c.(4675-4677)tCg>tTg | p.S1559L |
| SKCM | 14 | 20849204 | 20849204 | + | Splice_Site | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:20849204G>A | c.4648C>T | c.(4648-4650)Ctc>Ttc | p.L1550F |
| SKCM | 14 | 20850797 | 20850797 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:20850797G>A | c.4125C>T | c.(4123-4125)ttC>ttT | p.F1375F |
| SKCM | 14 | 20851703 | 20851703 | + | Silent | SNP | A | A | G | TCGA-EE-A2MT-06A-11D-A197-08 | TCGA-EE-A2MT-10A-01D-A199-08 | g.chr14:20851703A>G | c.3811T>C | c.(3811-3813)Tta>Cta | p.L1271L |
| SKCM | 14 | 20851800 | 20851800 | + | Silent | SNP | G | G | A | TCGA-ER-A19O-06A-11D-A197-08 | TCGA-ER-A19O-10A-01D-A199-08 | g.chr14:20851800G>A | c.3714C>T | c.(3712-3714)agC>agT | p.S1238S |
| SKCM | 14 | 20851952 | 20851952 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:20851952G>A | c.3660C>T | c.(3658-3660)acC>acT | p.T1220T |
| SKCM | 14 | 20852269 | 20852269 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-EE-A29N-06A-12D-A197-08 | TCGA-EE-A29N-10A-01D-A199-08 | g.chr14:20852269delT | c.3462delA | c.(3460-3462)caafs | p.Q1154fs |
| SKCM | 14 | 20852297 | 20852297 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29N-06A-12D-A197-08 | TCGA-EE-A29N-10A-01D-A199-08 | g.chr14:20852297C>T | c.3434G>A | c.(3433-3435)cGg>cAg | p.R1145Q |
| SKCM | 14 | 20852304 | 20852304 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr14:20852304G>A | c.3427C>T | c.(3427-3429)Cct>Tct | p.P1143S |
| SKCM | 14 | 20852647 | 20852647 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-D3-A2JL-06A-11D-A196-08 | TCGA-D3-A2JL-10A-01D-A198-08 | g.chr14:20852647delC | c.3242delG | c.(3241-3243)ggtfs | p.G1081fs |
| SKCM | 14 | 20852664 | 20852664 | + | Silent | SNP | G | G | A | TCGA-ER-A19E-06A-11D-A197-08 | TCGA-ER-A19E-10A-01D-A199-08 | g.chr14:20852664G>A | c.3225C>T | c.(3223-3225)taC>taT | p.Y1075Y |
| SKCM | 14 | 20853249 | 20853249 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A20B-06A-11D-A196-08 | TCGA-EE-A20B-10A-01D-A198-08 | g.chr14:20853249C>T | c.3002G>A | c.(3001-3003)gGg>gAg | p.G1001E |
| SKCM | 14 | 20853250 | 20853250 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A20B-06A-11D-A196-08 | TCGA-EE-A20B-10A-01D-A198-08 | g.chr14:20853250C>T | c.3001G>A | c.(3001-3003)Ggg>Agg | p.G1001R |
| SKCM | 14 | 20854287 | 20854287 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-D9-A1JW-06A-11D-A19A-08 | TCGA-D9-A1JW-10A-01D-A19A-08 | g.chr14:20854287delA | c.2929delT | c.(2929-2931)tatfs | p.Y977fs |
| SKCM | 14 | 20854292 | 20854292 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr14:20854292G>A | c.2924C>T | c.(2923-2925)tCc>tTc | p.S975F |
| SKCM | 14 | 20856088 | 20856088 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr14:20856088G>A | c.2660C>T | c.(2659-2661)cCc>cTc | p.P887L |
| SKCM | 14 | 20856143 | 20856143 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:20856143G>A | c.2605C>T | c.(2605-2607)Cca>Tca | p.P869S |
| SKCM | 14 | 20856222 | 20856222 | + | Splice_Site | SNP | C | C | G | TCGA-ER-A19D-06A-11D-A197-08 | TCGA-ER-A19D-10A-01D-A199-08 | g.chr14:20856222C>G | c.2526G>C | c.(2524-2526)aaG>aaC | p.K842N |
| SKCM | 14 | 20864104 | 20864104 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr14:20864104G>A | c.1664C>T | c.(1663-1665)tCg>tTg | p.S555L |
| SKCM | 14 | 20869274 | 20869274 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr14:20869274G>A | c.1418C>T | c.(1417-1419)tCt>tTt | p.S473F |
| SKCM | 14 | 20871883 | 20871883 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr14:20871883G>A | c.1193C>T | c.(1192-1194)cCa>cTa | p.P398L |
| SKCM | 14 | 20871927 | 20871927 | + | Silent | SNP | C | C | T | TCGA-EE-A3AD-06A-11D-A196-08 | TCGA-EE-A3AD-10A-01D-A198-08 | g.chr14:20871927C>T | c.1149G>A | c.(1147-1149)cgG>cgA | p.R383R |
| SKCM | 14 | 20872010 | 20872010 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr14:20872010G>A | c.1066C>T | c.(1066-1068)Ccc>Tcc | p.P356S |
| SKCM | 14 | 20873656 | 20873656 | + | Missense_Mutation | SNP | T | T | C | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr14:20873656T>C | c.824A>G | c.(823-825)gAa>gGa | p.E275G |
| SKCM | 14 | 20874556 | 20874556 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr14:20874556G>A | c.571C>T | c.(571-573)Cgt>Tgt | p.R191C |
| SKCM | 14 | 20876165 | 20876165 | + | Missense_Mutation | SNP | T | T | A | TCGA-D3-A5GL-06A-11D-A27K-08 | TCGA-D3-A5GL-10A-01D-A27N-08 | g.chr14:20876165T>A | c.434A>T | c.(433-435)aAc>aTc | p.N145I |
| SKCM | 14 | 20876287 | 20876287 | + | Silent | SNP | G | G | A | TCGA-D3-A2JK-06A-11D-A196-08 | TCGA-D3-A2JK-10A-01D-A198-08 | g.chr14:20876287G>A | c.312C>T | c.(310-312)atC>atT | p.I104I |
| SKCM | 14 | 20876479 | 20876479 | + | Silent | SNP | G | G | A | TCGA-D3-A3C8-06A-12D-A19A-08 | TCGA-D3-A3C8-10A-01D-A19A-08 | g.chr14:20876479G>A | c.120C>T | c.(118-120)acC>acT | p.T40T |