| 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 | 21 | 40667746 | 40667746 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-OR-A5J5-01A-11D-A29I-10 | TCGA-OR-A5J5-10A-01D-A29L-10 | g.chr21:40667746delT | c.532delA | c.(532-534)atgfs | p.M178fs |
| BLCA | 21 | 40559035 | 40559035 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chr21:40559035C>T | c.6880G>A | c.(6880-6882)Gaa>Aaa | p.E2294K |
| BLCA | 21 | 40559037 | 40559037 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A1A3-01A-11D-A13W-08 | TCGA-DK-A1A3-10A-01D-A13W-08 | g.chr21:40559037G>A | c.6878C>T | c.(6877-6879)tCt>tTt | p.S2293F |
| BLCA | 21 | 40559205 | 40559205 | + | Missense_Mutation | SNP | A | A | T | TCGA-XF-A9SZ-01A-11D-A391-08 | TCGA-XF-A9SZ-10A-01D-A394-08 | g.chr21:40559205A>T | c.6710T>A | c.(6709-6711)gTt>gAt | p.V2237D |
| BLCA | 21 | 40568278 | 40568278 | + | Intron | SNP | C | C | T | TCGA-BL-A13J-01A-11D-A10S-08 | TCGA-BL-A13J-10A-01D-A10S-08 | g.chr21:40568278C>T | | | |
| BLCA | 21 | 40569194 | 40569194 | + | Missense_Mutation | SNP | G | G | A | TCGA-FT-A3EE-01A-11D-A202-08 | TCGA-FT-A3EE-10A-01D-A202-08 | g.chr21:40569194G>A | c.5801C>T | c.(5800-5802)aCg>aTg | p.T1934M |
| BLCA | 21 | 40571073 | 40571073 | + | Missense_Mutation | SNP | C | C | T | TCGA-E5-A4U1-01A-11D-A31L-08 | TCGA-E5-A4U1-10B-01D-A31J-08 | g.chr21:40571073C>T | c.5269G>A | c.(5269-5271)Gag>Aag | p.E1757K |
| BLCA | 21 | 40574387 | 40574387 | + | Silent | SNP | C | C | T | TCGA-G2-A2ES-01A-11D-A17V-08 | TCGA-G2-A2ES-11A-31D-A17V-08 | g.chr21:40574387C>T | c.4449G>A | c.(4447-4449)agG>agA | p.R1483R |
| BLCA | 21 | 40578084 | 40578084 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A1A6-01A-11D-A13W-08 | TCGA-DK-A1A6-10A-01D-A13W-08 | g.chr21:40578084G>C | c.4314C>G | c.(4312-4314)ttC>ttG | p.F1438L |
| BLCA | 21 | 40581972 | 40581972 | + | Missense_Mutation | SNP | G | G | C | TCGA-4Z-AA80-01A-11D-A391-08 | TCGA-4Z-AA80-10A-01D-A394-08 | g.chr21:40581972G>C | c.4146C>G | c.(4144-4146)atC>atG | p.I1382M |
| BLCA | 21 | 40590434 | 40590434 | + | Missense_Mutation | SNP | G | G | T | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr21:40590434G>T | c.3535C>A | c.(3535-3537)Ctt>Att | p.L1179I |
| BLCA | 21 | 40590539 | 40590539 | + | Missense_Mutation | SNP | C | C | T | TCGA-GD-A6C6-01A-21D-A31L-08 | TCGA-GD-A6C6-10A-01D-A31J-08 | g.chr21:40590539C>T | c.3430G>A | c.(3430-3432)Gag>Aag | p.E1144K |
| BLCA | 21 | 40604198 | 40604198 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-BT-A20Q-01A-11D-A14W-08 | TCGA-BT-A20Q-11A-11D-A14W-08 | g.chr21:40604198G>A | c.2905C>T | c.(2905-2907)Cga>Tga | p.R969* |
| BLCA | 21 | 40622758 | 40622758 | + | Missense_Mutation | SNP | T | T | C | TCGA-XF-A9T0-01A-11D-A391-08 | TCGA-XF-A9T0-10A-01D-A394-08 | g.chr21:40622758T>C | c.2313A>G | c.(2311-2313)atA>atG | p.I771M |
| BLCA | 21 | 40627645 | 40627645 | + | Missense_Mutation | SNP | C | C | G | TCGA-GU-AATO-01A-11D-A391-08 | TCGA-GU-AATO-10A-01D-A394-08 | g.chr21:40627645C>G | c.2181G>C | c.(2179-2181)caG>caC | p.Q727H |
| BLCA | 21 | 40627734 | 40627734 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A3IT-01A-31D-A20D-08 | TCGA-DK-A3IT-10A-01D-A20D-08 | g.chr21:40627734C>G | c.2092G>C | c.(2092-2094)Gac>Cac | p.D698H |
| BLCA | 21 | 40636481 | 40636481 | + | Missense_Mutation | SNP | C | C | A | TCGA-DK-A1AD-01A-11D-A13W-08 | TCGA-DK-A1AD-10A-01D-A13W-08 | g.chr21:40636481C>A | c.1790G>T | c.(1789-1791)gGa>gTa | p.G597V |
| BLCA | 21 | 40636520 | 40636520 | + | Missense_Mutation | SNP | G | G | T | TCGA-E5-A2PC-01A-11D-A202-08 | TCGA-E5-A2PC-10B-01D-A202-08 | g.chr21:40636520G>T | c.1751C>A | c.(1750-1752)cCt>cAt | p.P584H |
| BLCA | 21 | 40636563 | 40636563 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1AD-01A-11D-A13W-08 | TCGA-DK-A1AD-10A-01D-A13W-08 | g.chr21:40636563C>T | c.1708G>A | c.(1708-1710)Gat>Aat | p.D570N |
| BLCA | 21 | 40636565 | 40636565 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1AD-01A-11D-A13W-08 | TCGA-DK-A1AD-10A-01D-A13W-08 | g.chr21:40636565C>T | c.1706G>A | c.(1705-1707)aGa>aAa | p.R569K |
| BLCA | 21 | 40636822 | 40636822 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1AD-01A-11D-A13W-08 | TCGA-DK-A1AD-10A-01D-A13W-08 | g.chr21:40636822C>T | c.1654G>A | c.(1654-1656)Gaa>Aaa | p.E552K |
| BLCA | 21 | 40636873 | 40636873 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A1AD-01A-11D-A13W-08 | TCGA-DK-A1AD-10A-01D-A13W-08 | g.chr21:40636873C>G | c.1603G>C | c.(1603-1605)Gat>Cat | p.D535H |
| BLCA | 21 | 40646305 | 40646305 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chr21:40646305G>C | c.1239C>G | c.(1237-1239)atC>atG | p.I413M |
| BLCA | 21 | 40650683 | 40650683 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A3PK-01A-21D-A21Z-08 | TCGA-BT-A3PK-10A-01D-A21Z-08 | g.chr21:40650683G>A | c.989C>T | c.(988-990)tCt>tTt | p.S330F |
| BLCA | 21 | 40650731 | 40650731 | + | Missense_Mutation | SNP | G | G | A | TCGA-YF-AA3M-01A-11D-A42E-08 | TCGA-YF-AA3M-10D-01D-A42H-08 | g.chr21:40650731G>A | c.941C>T | c.(940-942)cCc>cTc | p.P314L |
| BLCA | 21 | 40665770 | 40665770 | + | Silent | SNP | G | G | C | TCGA-KQ-A41Q-01A-11D-A339-08 | TCGA-KQ-A41Q-10D-01D-A339-08 | g.chr21:40665770G>C | c.798C>G | c.(796-798)ctC>ctG | p.L266L |
| BLCA | 21 | 40667668 | 40667668 | + | Splice_Site | SNP | C | C | G | TCGA-XF-A9SJ-01A-11D-A391-08 | TCGA-XF-A9SJ-10A-01D-A394-08 | g.chr21:40667668C>G | | c.e7+1 | |
| BLCA | 21 | 40670378 | 40670378 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-AA71-01A-31D-A391-08 | TCGA-DK-AA71-10A-01D-A394-08 | g.chr21:40670378G>C | c.329C>G | c.(328-330)tCt>tGt | p.S110C |
| BRCA | 21 | 40559077 | 40559078 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-AN-A0G0-01A-11W-A050-09 | TCGA-AN-A0G0-10A-01W-A055-09 | g.chr21:40559077_40559078insT | c.6837_6838insA | c.(6835-6840)aaattafs | p.L2280fs |
| BRCA | 21 | 40568403 | 40568403 | + | Intron | SNP | T | T | C | TCGA-AR-A5QM-01A-11D-A27P-09 | TCGA-AR-A5QM-10A-01D-A27P-09 | g.chr21:40568403T>C | | | |
| BRCA | 21 | 40569039 | 40569039 | + | Missense_Mutation | SNP | C | C | G | TCGA-A8-A09M-01A-11W-A019-09 | TCGA-A8-A09M-10A-01W-A021-09 | g.chr21:40569039C>G | c.5956G>C | c.(5956-5958)Gaa>Caa | p.E1986Q |
| BRCA | 21 | 40569277 | 40569277 | + | Silent | SNP | G | G | A | TCGA-AO-A12E-01A-11D-A10M-09 | TCGA-AO-A12E-10A-01D-A10M-09 | g.chr21:40569277G>A | c.5718C>T | c.(5716-5718)gaC>gaT | p.D1906D |
| BRCA | 21 | 40570751 | 40570751 | + | Missense_Mutation | SNP | C | C | T | TCGA-A2-A0CW-01A-21D-A10Y-09 | TCGA-A2-A0CW-10A-01D-A110-09 | g.chr21:40570751C>T | c.5591G>A | c.(5590-5592)gGa>gAa | p.G1864E |
| BRCA | 21 | 40570851 | 40570851 | + | Missense_Mutation | SNP | C | C | G | TCGA-A2-A0CW-01A-21D-A10Y-09 | TCGA-A2-A0CW-10A-01D-A110-09 | g.chr21:40570851C>G | c.5491G>C | c.(5491-5493)Gat>Cat | p.D1831H |
| BRCA | 21 | 40570878 | 40570878 | + | Missense_Mutation | SNP | A | A | C | TCGA-C8-A12W-01A-11D-A10Y-09 | TCGA-C8-A12W-10A-01D-A110-09 | g.chr21:40570878A>C | c.5464T>G | c.(5464-5466)Tca>Gca | p.S1822A |
| BRCA | 21 | 40570906 | 40570906 | + | Missense_Mutation | SNP | G | G | C | TCGA-D8-A27G-01A-11D-A16D-09 | TCGA-D8-A27G-10A-01D-A16D-09 | g.chr21:40570906G>C | c.5436C>G | c.(5434-5436)ttC>ttG | p.F1812L |
| BRCA | 21 | 40570950 | 40570950 | + | Missense_Mutation | SNP | A | A | T | TCGA-EW-A1IZ-01A-11D-A188-09 | TCGA-EW-A1IZ-10A-01D-A13O-09 | g.chr21:40570950A>T | c.5392T>A | c.(5392-5394)Tct>Act | p.S1798T |
| BRCA | 21 | 40571052 | 40571052 | + | Missense_Mutation | SNP | C | C | G | TCGA-E2-A573-01A-11D-A29N-09 | TCGA-E2-A573-10A-01D-A29N-09 | g.chr21:40571052C>G | c.5290G>C | c.(5290-5292)Gat>Cat | p.D1764H |
| BRCA | 21 | 40571202 | 40571202 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-A8-A08R-01A-11W-A050-09 | TCGA-A8-A08R-10A-01W-A055-09 | g.chr21:40571202C>A | c.5140G>T | c.(5140-5142)Gaa>Taa | p.E1714* |
| BRCA | 21 | 40571242 | 40571242 | + | Silent | SNP | T | T | C | TCGA-AO-A1KT-01A-11D-A13L-09 | TCGA-AO-A1KT-10A-01D-A188-09 | g.chr21:40571242T>C | c.5100A>G | c.(5098-5100)ttA>ttG | p.L1700L |
| BRCA | 21 | 40571393 | 40571393 | + | Missense_Mutation | SNP | G | G | C | TCGA-BH-A0DZ-01A-11W-A019-09 | TCGA-BH-A0DZ-10A-01W-A021-09 | g.chr21:40571393G>C | c.4949C>G | c.(4948-4950)tCt>tGt | p.S1650C |
| BRCA | 21 | 40571558 | 40571558 | + | Missense_Mutation | SNP | C | C | G | TCGA-A2-A0CW-01A-21D-A10Y-09 | TCGA-A2-A0CW-10A-01D-A110-09 | g.chr21:40571558C>G | c.4784G>C | c.(4783-4785)aGa>aCa | p.R1595T |
| BRCA | 21 | 40587280 | 40587280 | + | Missense_Mutation | SNP | G | G | C | TCGA-AN-A0XR-01A-11D-A10G-09 | TCGA-AN-A0XR-10A-01D-A117-09 | g.chr21:40587280G>C | c.3668C>G | c.(3667-3669)tCt>tGt | p.S1223C |
| BRCA | 21 | 40590186 | 40590186 | + | Missense_Mutation | SNP | G | G | C | TCGA-A2-A3Y0-01A-11D-A23C-09 | TCGA-A2-A3Y0-10A-01D-A23C-09 | g.chr21:40590186G>C | c.3551C>G | c.(3550-3552)gCt>gGt | p.A1184G |
| BRCA | 21 | 40590533 | 40590533 | + | Missense_Mutation | SNP | C | C | G | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr21:40590533C>G | c.3436G>C | c.(3436-3438)Gag>Cag | p.E1146Q |
| BRCA | 21 | 40597087 | 40597087 | + | Missense_Mutation | SNP | C | C | G | TCGA-E2-A574-01A-11D-A29N-09 | TCGA-E2-A574-10A-01D-A29N-09 | g.chr21:40597087C>G | c.3245G>C | c.(3244-3246)tGg>tCg | p.W1082S |
| BRCA | 21 | 40600483 | 40600484 | + | Frame_Shift_Del | DEL | CA | CA | - | TCGA-EW-A1P8-01A-11D-A142-09 | TCGA-EW-A1P8-10A-01D-A142-09 | g.chr21:40600483_40600484delCA | c.3150_3151delTG | c.(3148-3153)attgacfs | p.D1051fs |
| BRCA | 21 | 40619685 | 40619685 | + | Missense_Mutation | SNP | C | C | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr21:40619685C>A | c.2423G>T | c.(2422-2424)aGa>aTa | p.R808I |
| BRCA | 21 | 40646341 | 40646341 | + | Missense_Mutation | SNP | T | T | A | TCGA-D8-A1XQ-01A-11D-A14K-09 | TCGA-D8-A1XQ-10A-01D-A14K-09 | g.chr21:40646341T>A | c.1203A>T | c.(1201-1203)gaA>gaT | p.E401D |
| BRCA | 21 | 40665954 | 40665954 | + | Missense_Mutation | SNP | G | G | A | TCGA-AR-A2LE-01A-11D-A17W-09 | TCGA-AR-A2LE-10A-01D-A17W-09 | g.chr21:40665954G>A | c.614C>T | c.(613-615)tCa>tTa | p.S205L |
| BRCA | 21 | 40670464 | 40670464 | + | Silent | SNP | G | G | A | TCGA-C8-A1HE-01A-11D-A188-09 | TCGA-C8-A1HE-10A-01D-A13O-09 | g.chr21:40670464G>A | c.243C>T | c.(241-243)atC>atT | p.I81I |
| CESC | 21 | 40568805 | 40568805 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1BI-01B-11D-A13W-08 | TCGA-C5-A1BI-10A-01D-A13W-08 | g.chr21:40568805C>T | c.6190G>A | c.(6190-6192)Gag>Aag | p.E2064K |
| CESC | 21 | 40570860 | 40570860 | + | Missense_Mutation | SNP | C | C | T | TCGA-IR-A3LF-01A-21D-A22X-09 | TCGA-IR-A3LF-10A-01D-A22X-09 | g.chr21:40570860C>T | c.5482G>A | c.(5482-5484)Gaa>Aaa | p.E1828K |
| CESC | 21 | 40570985 | 40570985 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1MH-01A-11D-A14W-08 | TCGA-C5-A1MH-10A-01D-A14W-08 | g.chr21:40570985C>T | c.5357G>A | c.(5356-5358)aGc>aAc | p.S1786N |
| CESC | 21 | 40608645 | 40608645 | + | Missense_Mutation | SNP | C | C | G | TCGA-JX-A3Q0-01A-11D-A21Q-09 | TCGA-JX-A3Q0-10A-01D-A21Q-09 | g.chr21:40608645C>G | c.2642G>C | c.(2641-2643)aGa>aCa | p.R881T |
| CESC | 21 | 40619650 | 40619650 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr21:40619650C>T | c.2458G>A | c.(2458-2460)Gag>Aag | p.E820K |
| CESC | 21 | 40619736 | 40619736 | + | Missense_Mutation | SNP | G | G | A | TCGA-Q1-A6DW-01A-11D-A32I-09 | TCGA-Q1-A6DW-10B-01D-A32I-09 | g.chr21:40619736G>A | c.2372C>T | c.(2371-2373)tCa>tTa | p.S791L |
| CESC | 21 | 40630548 | 40630548 | + | Missense_Mutation | SNP | C | C | G | TCGA-C5-A1MK-01A-11D-A14W-08 | TCGA-C5-A1MK-10A-01D-A14W-08 | g.chr21:40630548C>G | c.1936G>C | c.(1936-1938)Gat>Cat | p.D646H |
| CESC | 21 | 40641950 | 40641950 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A2PG-01A-11D-A18J-09 | TCGA-EK-A2PG-10A-01D-A18J-09 | g.chr21:40641950C>T | c.1405G>A | c.(1405-1407)Gat>Aat | p.D469N |
| CESC | 21 | 40667817 | 40667817 | + | Missense_Mutation | SNP | C | C | G | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr21:40667817C>G | c.461G>C | c.(460-462)cGa>cCa | p.R154P |
| CHOL | 21 | 40665822 | 40665822 | + | Missense_Mutation | SNP | T | T | C | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr21:40665822T>C | c.746A>G | c.(745-747)gAt>gGt | p.D249G |
| CHOL | 21 | 40668258 | 40668258 | + | Silent | SNP | G | G | T | TCGA-W5-AA2R-01A-11D-A417-09 | TCGA-W5-AA2R-10A-01D-A41A-09 | g.chr21:40668258G>T | c.381C>A | c.(379-381)gcC>gcA | p.A127A |
| COAD | 21 | 40559106 | 40559106 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr21:40559106C>T | c.6809G>A | c.(6808-6810)cGa>cAa | p.R2270Q |
| COAD | 21 | 40559109 | 40559110 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-D5-6927-01A-21D-1924-10 | TCGA-D5-6927-10A-01D-1924-10 | g.chr21:40559109_40559110insG | c.6805_6806insC | c.(6805-6807)catfs | p.H2269fs |
| COAD | 21 | 40568256 | 40568256 | + | Intron | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr21:40568256C>T | | | |
| COAD | 21 | 40569293 | 40569294 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr21:40569293_40569294insT | c.5701_5702insA | c.(5701-5703)aggfs | p.R1901fs |
| COAD | 21 | 40571490 | 40571490 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr21:40571490G>T | c.4852C>A | c.(4852-4854)Cta>Ata | p.L1618I |
| COAD | 21 | 40572234 | 40572234 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr21:40572234G>A | c.4664C>T | c.(4663-4665)tCc>tTc | p.S1555F |
| COAD | 21 | 40578101 | 40578101 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr21:40578101G>A | c.4297C>T | c.(4297-4299)Cga>Tga | p.R1433* |
| COAD | 21 | 40578154 | 40578155 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr21:40578154_40578155insT | c.4243_4244insA | c.(4243-4245)atgfs | p.M1415fs |
| COAD | 21 | 40582061 | 40582061 | + | Missense_Mutation | SNP | T | T | C | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr21:40582061T>C | c.4057A>G | c.(4057-4059)Att>Gtt | p.I1353V |
| COAD | 21 | 40582780 | 40582780 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3530-01A-01W-0995-10 | TCGA-AA-3530-10A-01W-0995-10 | g.chr21:40582780C>T | c.3976G>A | c.(3976-3978)Gtg>Atg | p.V1326M |
| COAD | 21 | 40582819 | 40582819 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3527-01A-01W-0831-10 | TCGA-AA-3527-10A-01W-0831-10 | g.chr21:40582819A>G | c.3937T>C | c.(3937-3939)Tat>Cat | p.Y1313H |
| COAD | 21 | 40582836 | 40582837 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr21:40582836_40582837insT | c.3919_3920insA | c.(3919-3921)agcfs | p.S1307fs |
| COAD | 21 | 40587201 | 40587201 | + | Silent | SNP | T | T | C | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr21:40587201T>C | c.3747A>G | c.(3745-3747)tcA>tcG | p.S1249S |
| COAD | 21 | 40600468 | 40600468 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chr21:40600468G>A | c.3166C>T | c.(3166-3168)Cgt>Tgt | p.R1056C |
| COAD | 21 | 40601356 | 40601356 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr21:40601356C>A | c.3007G>T | c.(3007-3009)Gaa>Taa | p.E1003* |
| COAD | 21 | 40604127 | 40604127 | + | Silent | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr21:40604127C>T | c.2976G>A | c.(2974-2976)gaG>gaA | p.E992E |
| COAD | 21 | 40608628 | 40608628 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3821-01A-01W-0995-10 | TCGA-AA-3821-10A-01W-0995-10 | g.chr21:40608628G>A | c.2659C>T | c.(2659-2661)Cga>Tga | p.R887* |
| COAD | 21 | 40608663 | 40608663 | + | Missense_Mutation | SNP | T | T | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr21:40608663T>G | c.2624A>C | c.(2623-2625)aAt>aCt | p.N875T |
| COAD | 21 | 40610416 | 40610416 | + | Silent | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr21:40610416G>A | c.2565C>T | c.(2563-2565)agC>agT | p.S855S |
| COAD | 21 | 40636536 | 40636536 | + | Missense_Mutation | SNP | G | G | T | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr21:40636536G>T | c.1735C>A | c.(1735-1737)Caa>Aaa | p.Q579K |
| COAD | 21 | 40646359 | 40646359 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A1DB-01A-11D-A152-10 | TCGA-DM-A1DB-10A-01D-A152-10 | g.chr21:40646359C>A | c.1185G>T | c.(1183-1185)tgG>tgT | p.W395C |
| COAD | 21 | 40646360 | 40646360 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A28K-01A-21D-A16V-10 | TCGA-DM-A28K-10A-01D-A16V-10 | g.chr21:40646360C>A | c.1184G>T | c.(1183-1185)tGg>tTg | p.W395L |
| COAD | 21 | 40667674 | 40667675 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr21:40667674_40667675delAG | c.603_604delCT | c.(601-606)atctttfs | p.F202fs |
| COAD | 21 | 40667675 | 40667675 | + | Silent | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr21:40667675G>T | c.603C>A | c.(601-603)atC>atA | p.I201I |
| COAD | 21 | 40670402 | 40670402 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr21:40670402G>T | c.305C>A | c.(304-306)tCt>tAt | p.S102Y |
| COADREAD | 21 | 40559097 | 40559097 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr21:40559097G>T | c.6818C>A | c.(6817-6819)tCt>tAt | p.S2273Y |
| COADREAD | 21 | 40559106 | 40559106 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr21:40559106C>T | c.6809G>A | c.(6808-6810)cGa>cAa | p.R2270Q |
| COADREAD | 21 | 40559109 | 40559110 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-D5-6927-01A-21D-1924-10 | TCGA-D5-6927-10A-01D-1924-10 | g.chr21:40559109_40559110insG | c.6805_6806insC | c.(6805-6807)catfs | p.H2269fs |
| COADREAD | 21 | 40568256 | 40568256 | + | Intron | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr21:40568256C>T | | | |
| COADREAD | 21 | 40568294 | 40568294 | + | Intron | SNP | C | C | T | TCGA-DC-6682-01A-11D-1826-10 | TCGA-DC-6682-10A-01D-1826-10 | g.chr21:40568294C>T | | | |
| COADREAD | 21 | 40569293 | 40569294 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr21:40569293_40569294insT | c.5701_5702insA | c.(5701-5703)aggfs | p.R1901fs |
| COADREAD | 21 | 40570895 | 40570895 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr21:40570895G>T | c.5447C>A | c.(5446-5448)aCc>aAc | p.T1816N |
| COADREAD | 21 | 40571490 | 40571490 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr21:40571490G>T | c.4852C>A | c.(4852-4854)Cta>Ata | p.L1618I |
| COADREAD | 21 | 40572234 | 40572234 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr21:40572234G>A | c.4664C>T | c.(4663-4665)tCc>tTc | p.S1555F |
| COADREAD | 21 | 40578101 | 40578101 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr21:40578101G>A | c.4297C>T | c.(4297-4299)Cga>Tga | p.R1433* |
| COADREAD | 21 | 40578154 | 40578155 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr21:40578154_40578155insT | c.4243_4244insA | c.(4243-4245)atgfs | p.M1415fs |
| COADREAD | 21 | 40578199 | 40578199 | + | Splice_Site | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr21:40578199A>C | c.4199T>G | c.(4198-4200)aTt>aGt | p.I1400S |
| COADREAD | 21 | 40582061 | 40582061 | + | Missense_Mutation | SNP | T | T | C | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr21:40582061T>C | c.4057A>G | c.(4057-4059)Att>Gtt | p.I1353V |
| COADREAD | 21 | 40582780 | 40582780 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3530-01A-01W-0995-10 | TCGA-AA-3530-10A-01W-0995-10 | g.chr21:40582780C>T | c.3976G>A | c.(3976-3978)Gtg>Atg | p.V1326M |
| COADREAD | 21 | 40582819 | 40582819 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3527-01A-01W-0831-10 | TCGA-AA-3527-10A-01W-0831-10 | g.chr21:40582819A>G | c.3937T>C | c.(3937-3939)Tat>Cat | p.Y1313H |
| COADREAD | 21 | 40582836 | 40582837 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr21:40582836_40582837insT | c.3919_3920insA | c.(3919-3921)agcfs | p.S1307fs |
| COADREAD | 21 | 40587201 | 40587201 | + | Silent | SNP | T | T | C | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr21:40587201T>C | c.3747A>G | c.(3745-3747)tcA>tcG | p.S1249S |
| COADREAD | 21 | 40587276 | 40587276 | + | Silent | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr21:40587276C>T | c.3672G>A | c.(3670-3672)gcG>gcA | p.A1224A |
| COADREAD | 21 | 40600468 | 40600468 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chr21:40600468G>A | c.3166C>T | c.(3166-3168)Cgt>Tgt | p.R1056C |
| COADREAD | 21 | 40601356 | 40601356 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr21:40601356C>A | c.3007G>T | c.(3007-3009)Gaa>Taa | p.E1003* |
| COADREAD | 21 | 40604127 | 40604127 | + | Silent | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr21:40604127C>T | c.2976G>A | c.(2974-2976)gaG>gaA | p.E992E |
| COADREAD | 21 | 40608628 | 40608628 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3821-01A-01W-0995-10 | TCGA-AA-3821-10A-01W-0995-10 | g.chr21:40608628G>A | c.2659C>T | c.(2659-2661)Cga>Tga | p.R887* |
| COADREAD | 21 | 40608663 | 40608663 | + | Missense_Mutation | SNP | T | T | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr21:40608663T>G | c.2624A>C | c.(2623-2625)aAt>aCt | p.N875T |
| COADREAD | 21 | 40610416 | 40610416 | + | Silent | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr21:40610416G>A | c.2565C>T | c.(2563-2565)agC>agT | p.S855S |
| COADREAD | 21 | 40610476 | 40610476 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A01Y-01A-41W-A096-10 | TCGA-AG-A01Y-11A-11W-A096-10 | g.chr21:40610476T>G | c.2505A>C | c.(2503-2505)gaA>gaC | p.E835D |
| COADREAD | 21 | 40636536 | 40636536 | + | Missense_Mutation | SNP | G | G | T | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr21:40636536G>T | c.1735C>A | c.(1735-1737)Caa>Aaa | p.Q579K |
| COADREAD | 21 | 40646359 | 40646359 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A1DB-01A-11D-A152-10 | TCGA-DM-A1DB-10A-01D-A152-10 | g.chr21:40646359C>A | c.1185G>T | c.(1183-1185)tgG>tgT | p.W395C |
| COADREAD | 21 | 40646360 | 40646360 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A28K-01A-21D-A16V-10 | TCGA-DM-A28K-10A-01D-A16V-10 | g.chr21:40646360C>A | c.1184G>T | c.(1183-1185)tGg>tTg | p.W395L |
| COADREAD | 21 | 40667674 | 40667675 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr21:40667674_40667675delAG | c.603_604delCT | c.(601-606)atctttfs | p.F202fs |
| COADREAD | 21 | 40667675 | 40667675 | + | Silent | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr21:40667675G>T | c.603C>A | c.(601-603)atC>atA | p.I201I |
| COADREAD | 21 | 40670402 | 40670402 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr21:40670402G>T | c.305C>A | c.(304-306)tCt>tAt | p.S102Y |
| DLBC | 21 | 40570830 | 40570830 | + | Missense_Mutation | SNP | G | G | C | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr21:40570830G>C | c.5512C>G | c.(5512-5514)Cat>Gat | p.H1838D |
| DLBC | 21 | 40574434 | 40574434 | + | Missense_Mutation | SNP | T | T | C | TCGA-GR-7353-01A-11D-2210-10 | TCGA-GR-7353-10A-01D-2210-10 | g.chr21:40574434T>C | c.4402A>G | c.(4402-4404)Ata>Gta | p.I1468V |
| DLBC | 21 | 40582823 | 40582823 | + | Silent | SNP | C | C | T | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr21:40582823C>T | c.3933G>A | c.(3931-3933)acG>acA | p.T1311T |
| DLBC | 21 | 40590176 | 40590176 | + | Silent | SNP | G | G | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr21:40590176G>T | c.3561C>A | c.(3559-3561)ggC>ggA | p.G1187G |
| DLBC | 21 | 40608530 | 40608530 | + | Silent | SNP | A | A | C | TCGA-G8-6909-01A-11D-2210-10 | TCGA-G8-6909-14A-01D-2210-10 | g.chr21:40608530A>C | c.2757T>G | c.(2755-2757)ccT>ccG | p.P919P |
| ESCA | 21 | 40569302 | 40569302 | + | Missense_Mutation | SNP | G | G | A | TCGA-JY-A6FB-01A-11D-A33E-09 | TCGA-JY-A6FB-10A-01D-A33H-09 | g.chr21:40569302G>A | c.5693C>T | c.(5692-5694)tCc>tTc | p.S1898F |
| ESCA | 21 | 40571099 | 40571099 | + | Missense_Mutation | SNP | G | G | T | TCGA-VR-A8EZ-01A-11D-A36J-09 | TCGA-VR-A8EZ-10A-01D-A36M-09 | g.chr21:40571099G>T | c.5243C>A | c.(5242-5244)aCa>aAa | p.T1748K |
| ESCA | 21 | 40571465 | 40571465 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A8I0-01A-11D-A36J-09 | TCGA-LN-A8I0-10A-01D-A36M-09 | g.chr21:40571465C>T | c.4877G>A | c.(4876-4878)cGa>cAa | p.R1626Q |
| ESCA | 21 | 40587221 | 40587221 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-JY-A6F8-01A-11D-A33E-09 | TCGA-JY-A6F8-10A-01D-A33H-09 | g.chr21:40587221C>A | c.3727G>T | c.(3727-3729)Gag>Tag | p.E1243* |
| ESCA | 21 | 40590524 | 40590524 | + | Missense_Mutation | SNP | G | G | A | TCGA-R6-A6DQ-01B-11D-A31U-09 | TCGA-R6-A6DQ-10A-01D-A31U-09 | g.chr21:40590524G>A | c.3445C>T | c.(3445-3447)Ctc>Ttc | p.L1149F |
| ESCA | 21 | 40619643 | 40619643 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr21:40619643G>A | c.2465C>T | c.(2464-2466)tCa>tTa | p.S822L |
| GBM | 21 | 40571510 | 40571510 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-16-1045-01B-01W-0611-08 | TCGA-16-1045-10B-01W-0611-08 | g.chr21:40571510G>T | c.4832C>A | c.(4831-4833)tCa>tAa | p.S1611* |
| GBMLGG | 21 | 40568686 | 40568686 | + | Silent | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40568686G>T | c.6309C>A | c.(6307-6309)acC>acA | p.T2103T |
| GBMLGG | 21 | 40570809 | 40570809 | + | Missense_Mutation | SNP | T | T | C | TCGA-S9-A6WO-01A-21D-A34A-08 | TCGA-S9-A6WO-10A-01D-A34A-08 | g.chr21:40570809T>C | c.5533A>G | c.(5533-5535)Att>Gtt | p.I1845V |
| GBMLGG | 21 | 40570895 | 40570895 | + | Missense_Mutation | SNP | G | G | T | TCGA-FG-A710-01A-12D-A33T-08 | TCGA-FG-A710-10A-01D-A33W-08 | g.chr21:40570895G>T | c.5447C>A | c.(5446-5448)aCc>aAc | p.T1816N |
| GBMLGG | 21 | 40571510 | 40571510 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-16-1045-01B-01W-0611-08 | TCGA-16-1045-10B-01W-0611-08 | g.chr21:40571510G>T | c.4832C>A | c.(4831-4833)tCa>tAa | p.S1611* |
| GBMLGG | 21 | 40572205 | 40572205 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40572205C>T | c.4693G>A | c.(4693-4695)Ggg>Agg | p.G1565R |
| GBMLGG | 21 | 40578093 | 40578093 | + | Missense_Mutation | SNP | G | G | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40578093G>C | c.4305C>G | c.(4303-4305)agC>agG | p.S1435R |
| GBMLGG | 21 | 40587227 | 40587227 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40587227C>T | c.3721G>A | c.(3721-3723)Gaa>Aaa | p.E1241K |
| GBMLGG | 21 | 40590181 | 40590181 | + | Missense_Mutation | SNP | C | C | T | TCGA-E1-5318-01A-01D-1468-08 | TCGA-E1-5318-10A-01D-1468-08 | g.chr21:40590181C>T | c.3556G>A | c.(3556-3558)Gca>Aca | p.A1186T |
| GBMLGG | 21 | 40604415 | 40604415 | + | Missense_Mutation | SNP | T | T | C | TCGA-QH-A6CZ-01A-11D-A32B-08 | TCGA-QH-A6CZ-10B-01D-A329-08 | g.chr21:40604415T>C | c.2776A>G | c.(2776-2778)Agg>Ggg | p.R926G |
| GBMLGG | 21 | 40610438 | 40610438 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40610438T>C | c.2543A>G | c.(2542-2544)gAc>gGc | p.D848G |
| GBMLGG | 21 | 40630542 | 40630542 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40630542G>A | c.1942C>T | c.(1942-1944)Cgc>Tgc | p.R648C |
| GBMLGG | 21 | 40670402 | 40670402 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40670402G>T | c.305C>A | c.(304-306)tCt>tAt | p.S102Y |
| GBMLGG | 21 | 40670456 | 40670456 | + | Missense_Mutation | SNP | C | C | T | TCGA-KT-A74X-01A-11D-A32B-08 | TCGA-KT-A74X-10A-01D-A329-08 | g.chr21:40670456C>T | c.251G>A | c.(250-252)cGc>cAc | p.R84H |
| GBMLGG | 21 | 40685224 | 40685224 | + | Splice_Site | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40685224C>A | c.51G>T | c.(49-51)gaG>gaT | p.E17D |
| HNSC | 21 | 40558961 | 40558961 | + | Silent | SNP | A | A | G | TCGA-CN-A497-01A-11D-A24D-08 | TCGA-CN-A497-10A-01D-A24F-08 | g.chr21:40558961A>G | c.6954T>C | c.(6952-6954)aaT>aaC | p.N2318N |
| HNSC | 21 | 40559107 | 40559107 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CV-A6JD-01A-11D-A31L-08 | TCGA-CV-A6JD-10A-01D-A31J-08 | g.chr21:40559107G>A | c.6808C>T | c.(6808-6810)Cga>Tga | p.R2270* |
| HNSC | 21 | 40568320 | 40568320 | + | Intron | SNP | A | A | G | TCGA-CR-6492-01A-12D-2078-08 | TCGA-CR-6492-10A-01D-2078-08 | g.chr21:40568320A>G | | | |
| HNSC | 21 | 40571183 | 40571183 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-P3-A5QF-01A-11D-A28R-08 | TCGA-P3-A5QF-10A-01D-A28U-08 | g.chr21:40571183G>C | c.5159C>G | c.(5158-5160)tCa>tGa | p.S1720* |
| HNSC | 21 | 40572223 | 40572223 | + | Missense_Mutation | SNP | C | C | T | TCGA-CX-7086-01A-11D-2078-08 | TCGA-CX-7086-10D-01D-2078-08 | g.chr21:40572223C>T | c.4675G>A | c.(4675-4677)Gaa>Aaa | p.E1559K |
| HNSC | 21 | 40574319 | 40574319 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-CN-4723-01A-01D-1434-08 | TCGA-CN-4723-10A-01D-1434-08 | g.chr21:40574319G>C | c.4517C>G | c.(4516-4518)tCa>tGa | p.S1506* |
| HNSC | 21 | 40578121 | 40578121 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr21:40578121T>C | c.4277A>G | c.(4276-4278)cAa>cGa | p.Q1426R |
| HNSC | 21 | 40604128 | 40604128 | + | Missense_Mutation | SNP | T | T | A | TCGA-CR-6478-01A-11D-1870-08 | TCGA-CR-6478-10A-01D-1870-08 | g.chr21:40604128T>A | c.2975A>T | c.(2974-2976)gAg>gTg | p.E992V |
| HNSC | 21 | 40610451 | 40610451 | + | Missense_Mutation | SNP | C | C | T | TCGA-UF-A719-01A-12D-A34J-08 | TCGA-UF-A719-10A-01D-A34M-08 | g.chr21:40610451C>T | c.2530G>A | c.(2530-2532)Gaa>Aaa | p.E844K |
| HNSC | 21 | 40627656 | 40627656 | + | Missense_Mutation | SNP | G | G | C | TCGA-KU-A66S-01A-21D-A30E-08 | TCGA-KU-A66S-10A-01D-A30H-08 | g.chr21:40627656G>C | c.2170C>G | c.(2170-2172)Cca>Gca | p.P724A |
| HNSC | 21 | 40630422 | 40630422 | + | Missense_Mutation | SNP | G | G | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr21:40630422G>A | c.2062C>T | c.(2062-2064)Ccc>Tcc | p.P688S |
| HNSC | 21 | 40649223 | 40649223 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CV-A6K1-01A-11D-A31L-08 | TCGA-CV-A6K1-10A-01D-A31J-08 | g.chr21:40649223delA | c.1058delT | c.(1057-1059)ttgfs | p.L353fs |
| HNSC | 21 | 40650700 | 40650700 | + | Silent | SNP | G | G | A | TCGA-CR-7383-01A-11D-2129-08 | TCGA-CR-7383-10A-01D-2129-08 | g.chr21:40650700G>A | c.972C>T | c.(970-972)ggC>ggT | p.G324G |
| HNSC | 21 | 40650738 | 40650738 | + | Splice_Site | SNP | G | G | A | TCGA-HD-8634-01A-11D-2394-08 | TCGA-HD-8634-10A-01D-2394-08 | g.chr21:40650738G>A | c.934C>T | c.(934-936)Cca>Tca | p.P312S |
| HNSC | 21 | 40667757 | 40667757 | + | Missense_Mutation | SNP | T | T | A | TCGA-CV-A6JU-01A-11D-A31L-08 | TCGA-CV-A6JU-10A-01D-A31J-08 | g.chr21:40667757T>A | c.521A>T | c.(520-522)cAg>cTg | p.Q174L |
| KICH | 21 | 40649185 | 40649185 | + | Missense_Mutation | SNP | T | T | C | TCGA-KL-8332-01A-11D-2310-10 | TCGA-KL-8332-11A-01D-2310-10 | g.chr21:40649185T>C | c.1096A>G | c.(1096-1098)Agc>Ggc | p.S366G |
| KIPAN | 21 | 40559338 | 40559338 | + | Missense_Mutation | SNP | C | C | A | TCGA-CZ-5459-01A-01D-1501-10 | TCGA-CZ-5459-11A-01D-1501-10 | g.chr21:40559338C>A | c.6577G>T | c.(6577-6579)Gtt>Ttt | p.V2193F |
| KIPAN | 21 | 40568354 | 40568354 | + | Intron | SNP | C | C | A | TCGA-CW-5589-01A-01D-1534-10 | TCGA-CW-5589-11A-01D-1535-10 | g.chr21:40568354C>A | | | |
| KIPAN | 21 | 40568620 | 40568620 | + | Missense_Mutation | SNP | T | T | G | TCGA-CJ-5682-01A-11D-1534-10 | TCGA-CJ-5682-11A-01D-1535-10 | g.chr21:40568620T>G | c.6375A>C | c.(6373-6375)gaA>gaC | p.E2125D |
| KIPAN | 21 | 40568695 | 40568695 | + | Silent | SNP | T | T | C | TCGA-CZ-5460-01A-01D-1501-10 | TCGA-CZ-5460-11A-01D-1501-10 | g.chr21:40568695T>C | c.6300A>G | c.(6298-6300)agA>agG | p.R2100R |
| KIPAN | 21 | 40571019 | 40571019 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-4176-01A-02D-1366-10 | TCGA-BP-4176-11A-01D-1366-10 | g.chr21:40571019G>T | c.5323C>A | c.(5323-5325)Cca>Aca | p.P1775T |
| KIPAN | 21 | 40572254 | 40572254 | + | Silent | SNP | A | A | G | TCGA-B0-4852-01A-01D-1501-10 | TCGA-B0-4852-11A-01D-1501-10 | g.chr21:40572254A>G | c.4644T>C | c.(4642-4644)tcT>tcC | p.S1548S |
| KIPAN | 21 | 40582046 | 40582046 | + | Missense_Mutation | SNP | T | T | C | TCGA-B4-5844-01A-11D-1669-08 | TCGA-B4-5844-10A-01D-1669-08 | g.chr21:40582046T>C | c.4072A>G | c.(4072-4074)Atg>Gtg | p.M1358V |
| KIPAN | 21 | 40590148 | 40590148 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-4989-01A-01D-1462-08 | TCGA-BP-4989-11A-01D-1462-08 | g.chr21:40590148A>G | c.3589T>C | c.(3589-3591)Tac>Cac | p.Y1197H |
| KIPAN | 21 | 40636400 | 40636400 | + | Missense_Mutation | SNP | C | C | G | TCGA-A3-3357-01A-02D-1421-08 | TCGA-A3-3357-11A-01D-1421-08 | g.chr21:40636400C>G | c.1871G>C | c.(1870-1872)gGc>gCc | p.G624A |
| KIPAN | 21 | 40641908 | 40641908 | + | Missense_Mutation | SNP | T | T | A | TCGA-IZ-8196-01A-11D-2396-08 | TCGA-IZ-8196-10A-01D-2396-08 | g.chr21:40641908T>A | c.1447A>T | c.(1447-1449)Att>Ttt | p.I483F |
| KIPAN | 21 | 40649185 | 40649185 | + | Missense_Mutation | SNP | T | T | C | TCGA-KL-8332-01A-11D-2310-10 | TCGA-KL-8332-11A-01D-2310-10 | g.chr21:40649185T>C | c.1096A>G | c.(1096-1098)Agc>Ggc | p.S366G |
| KIPAN | 21 | 40649200 | 40649200 | + | Missense_Mutation | SNP | T | T | G | TCGA-CJ-4635-01A-02D-1373-10 | TCGA-CJ-4635-11B-01D-1373-10 | g.chr21:40649200T>G | c.1081A>C | c.(1081-1083)Atc>Ctc | p.I361L |
| KIPAN | 21 | 40665927 | 40665927 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-B1-A655-01A-11D-A31Z-10 | TCGA-B1-A655-10A-01D-A31X-10 | g.chr21:40665927G>T | c.641C>A | c.(640-642)tCa>tAa | p.S214* |
| KIPAN | 21 | 40670471 | 40670471 | + | Missense_Mutation | SNP | A | A | C | TCGA-PJ-A8JU-01A-11D-A35Z-10 | TCGA-PJ-A8JU-10A-01D-A35Z-10 | g.chr21:40670471A>C | c.236T>G | c.(235-237)tTg>tGg | p.L79W |
| KIRC | 21 | 40559338 | 40559338 | + | Missense_Mutation | SNP | C | C | A | TCGA-CZ-5459-01A-01D-1501-10 | TCGA-CZ-5459-11A-01D-1501-10 | g.chr21:40559338C>A | c.6577G>T | c.(6577-6579)Gtt>Ttt | p.V2193F |
| KIRC | 21 | 40568354 | 40568354 | + | Intron | SNP | C | C | A | TCGA-CW-5589-01A-01D-1534-10 | TCGA-CW-5589-11A-01D-1535-10 | g.chr21:40568354C>A | | | |
| KIRC | 21 | 40568620 | 40568620 | + | Missense_Mutation | SNP | T | T | G | TCGA-CJ-5682-01A-11D-1534-10 | TCGA-CJ-5682-11A-01D-1535-10 | g.chr21:40568620T>G | c.6375A>C | c.(6373-6375)gaA>gaC | p.E2125D |
| KIRC | 21 | 40568695 | 40568695 | + | Silent | SNP | T | T | C | TCGA-CZ-5460-01A-01D-1501-10 | TCGA-CZ-5460-11A-01D-1501-10 | g.chr21:40568695T>C | c.6300A>G | c.(6298-6300)agA>agG | p.R2100R |
| KIRC | 21 | 40571019 | 40571019 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-4176-01A-02D-1366-10 | TCGA-BP-4176-11A-01D-1366-10 | g.chr21:40571019G>T | c.5323C>A | c.(5323-5325)Cca>Aca | p.P1775T |
| KIRC | 21 | 40572254 | 40572254 | + | Silent | SNP | A | A | G | TCGA-B0-4852-01A-01D-1501-10 | TCGA-B0-4852-11A-01D-1501-10 | g.chr21:40572254A>G | c.4644T>C | c.(4642-4644)tcT>tcC | p.S1548S |
| KIRC | 21 | 40582046 | 40582046 | + | Missense_Mutation | SNP | T | T | C | TCGA-B4-5844-01A-11D-1669-08 | TCGA-B4-5844-10A-01D-1669-08 | g.chr21:40582046T>C | c.4072A>G | c.(4072-4074)Atg>Gtg | p.M1358V |
| KIRC | 21 | 40590148 | 40590148 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-4989-01A-01D-1462-08 | TCGA-BP-4989-11A-01D-1462-08 | g.chr21:40590148A>G | c.3589T>C | c.(3589-3591)Tac>Cac | p.Y1197H |
| KIRC | 21 | 40636400 | 40636400 | + | Missense_Mutation | SNP | C | C | G | TCGA-A3-3357-01A-02D-1421-08 | TCGA-A3-3357-11A-01D-1421-08 | g.chr21:40636400C>G | c.1871G>C | c.(1870-1872)gGc>gCc | p.G624A |
| KIRC | 21 | 40649200 | 40649200 | + | Missense_Mutation | SNP | T | T | G | TCGA-CJ-4635-01A-02D-1373-10 | TCGA-CJ-4635-11B-01D-1373-10 | g.chr21:40649200T>G | c.1081A>C | c.(1081-1083)Atc>Ctc | p.I361L |
| KIRP | 21 | 40641908 | 40641908 | + | Missense_Mutation | SNP | T | T | A | TCGA-IZ-8196-01A-11D-2396-08 | TCGA-IZ-8196-10A-01D-2396-08 | g.chr21:40641908T>A | c.1447A>T | c.(1447-1449)Att>Ttt | p.I483F |
| KIRP | 21 | 40665927 | 40665927 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-B1-A655-01A-11D-A31Z-10 | TCGA-B1-A655-10A-01D-A31X-10 | g.chr21:40665927G>T | c.641C>A | c.(640-642)tCa>tAa | p.S214* |
| KIRP | 21 | 40670471 | 40670471 | + | Missense_Mutation | SNP | A | A | C | TCGA-PJ-A8JU-01A-11D-A35Z-10 | TCGA-PJ-A8JU-10A-01D-A35Z-10 | g.chr21:40670471A>C | c.236T>G | c.(235-237)tTg>tGg | p.L79W |
| LGG | 21 | 40568686 | 40568686 | + | Silent | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40568686G>T | c.6309C>A | c.(6307-6309)acC>acA | p.T2103T |
| LGG | 21 | 40570809 | 40570809 | + | Missense_Mutation | SNP | T | T | C | TCGA-S9-A6WO-01A-21D-A34A-08 | TCGA-S9-A6WO-10A-01D-A34A-08 | g.chr21:40570809T>C | c.5533A>G | c.(5533-5535)Att>Gtt | p.I1845V |
| LGG | 21 | 40570895 | 40570895 | + | Missense_Mutation | SNP | G | G | T | TCGA-FG-A710-01A-12D-A33T-08 | TCGA-FG-A710-10A-01D-A33W-08 | g.chr21:40570895G>T | c.5447C>A | c.(5446-5448)aCc>aAc | p.T1816N |
| LGG | 21 | 40572205 | 40572205 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40572205C>T | c.4693G>A | c.(4693-4695)Ggg>Agg | p.G1565R |
| LGG | 21 | 40578093 | 40578093 | + | Missense_Mutation | SNP | G | G | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40578093G>C | c.4305C>G | c.(4303-4305)agC>agG | p.S1435R |
| LGG | 21 | 40587227 | 40587227 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40587227C>T | c.3721G>A | c.(3721-3723)Gaa>Aaa | p.E1241K |
| LGG | 21 | 40590181 | 40590181 | + | Missense_Mutation | SNP | C | C | T | TCGA-E1-5318-01A-01D-1468-08 | TCGA-E1-5318-10A-01D-1468-08 | g.chr21:40590181C>T | c.3556G>A | c.(3556-3558)Gca>Aca | p.A1186T |
| LGG | 21 | 40604415 | 40604415 | + | Missense_Mutation | SNP | T | T | C | TCGA-QH-A6CZ-01A-11D-A32B-08 | TCGA-QH-A6CZ-10B-01D-A329-08 | g.chr21:40604415T>C | c.2776A>G | c.(2776-2778)Agg>Ggg | p.R926G |
| LGG | 21 | 40610438 | 40610438 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40610438T>C | c.2543A>G | c.(2542-2544)gAc>gGc | p.D848G |
| LGG | 21 | 40630542 | 40630542 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40630542G>A | c.1942C>T | c.(1942-1944)Cgc>Tgc | p.R648C |
| LGG | 21 | 40670402 | 40670402 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40670402G>T | c.305C>A | c.(304-306)tCt>tAt | p.S102Y |
| LGG | 21 | 40670456 | 40670456 | + | Missense_Mutation | SNP | C | C | T | TCGA-KT-A74X-01A-11D-A32B-08 | TCGA-KT-A74X-10A-01D-A329-08 | g.chr21:40670456C>T | c.251G>A | c.(250-252)cGc>cAc | p.R84H |
| LGG | 21 | 40685224 | 40685224 | + | Splice_Site | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr21:40685224C>A | c.51G>T | c.(49-51)gaG>gaT | p.E17D |
| LIHC | 21 | 40558988 | 40558988 | + | Missense_Mutation | SNP | T | T | G | TCGA-DD-AAVZ-01A-11D-A40R-10 | TCGA-DD-AAVZ-10A-01D-A40U-10 | g.chr21:40558988T>G | c.6927A>C | c.(6925-6927)ttA>ttC | p.L2309F |
| LIHC | 21 | 40568678 | 40568678 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AACG-01A-11D-A40R-10 | TCGA-DD-AACG-10A-01D-A40U-10 | g.chr21:40568678T>C | c.6317A>G | c.(6316-6318)aAg>aGg | p.K2106R |
| LIHC | 21 | 40568902 | 40568902 | + | Silent | SNP | C | C | T | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr21:40568902C>T | c.6093G>A | c.(6091-6093)agG>agA | p.R2031R |
| LIHC | 21 | 40570714 | 40570714 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AADD-01A-11D-A40R-10 | TCGA-DD-AADD-10A-01D-A40U-10 | g.chr21:40570714T>C | c.5628A>G | c.(5626-5628)atA>atG | p.I1876M |
| LIHC | 21 | 40571299 | 40571299 | + | Silent | SNP | T | T | C | TCGA-BC-A3KG-01A-11D-A20W-10 | TCGA-BC-A3KG-10A-01D-A20W-10 | g.chr21:40571299T>C | c.5043A>G | c.(5041-5043)gaA>gaG | p.E1681E |
| LIHC | 21 | 40590495 | 40590495 | + | Silent | SNP | A | A | G | TCGA-CC-A3MB-01A-11D-A20W-10 | TCGA-CC-A3MB-10A-01D-A20W-10 | g.chr21:40590495A>G | c.3474T>C | c.(3472-3474)ggT>ggC | p.G1158G |
| LIHC | 21 | 40608663 | 40608663 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AACH-01A-11D-A40R-10 | TCGA-DD-AACH-10A-01D-A40U-10 | g.chr21:40608663T>C | c.2624A>G | c.(2623-2625)aAt>aGt | p.N875S |
| LIHC | 21 | 40619671 | 40619671 | + | Missense_Mutation | SNP | G | G | T | TCGA-K7-A6G5-01A-11D-A30V-10 | TCGA-K7-A6G5-10A-01D-A30V-10 | g.chr21:40619671G>T | c.2437C>A | c.(2437-2439)Cgt>Agt | p.R813S |
| LIHC | 21 | 40627715 | 40627715 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A3A7-01A-11D-A22F-10 | TCGA-DD-A3A7-11A-11D-A22F-10 | g.chr21:40627715T>C | c.2111A>G | c.(2110-2112)aAt>aGt | p.N704S |
| LUAD | 21 | 40559157 | 40559157 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr21:40559157G>C | c.6758C>G | c.(6757-6759)tCa>tGa | p.S2253* |
| LUAD | 21 | 40559292 | 40559292 | + | Missense_Mutation | SNP | T | T | A | TCGA-97-7938-01A-11D-2167-08 | TCGA-97-7938-10A-01D-2167-08 | g.chr21:40559292T>A | c.6623A>T | c.(6622-6624)cAt>cTt | p.H2208L |
| LUAD | 21 | 40568221 | 40568221 | + | Intron | SNP | T | T | A | TCGA-55-A492-01A-11D-A24D-08 | TCGA-55-A492-10A-01D-A24F-08 | g.chr21:40568221T>A | | | |
| LUAD | 21 | 40568276 | 40568276 | + | Intron | SNP | C | C | G | TCGA-55-6968-01A-11D-1945-08 | TCGA-55-6968-11A-01D-1945-08 | g.chr21:40568276C>G | | | |
| LUAD | 21 | 40568393 | 40568393 | + | Intron | SNP | G | G | A | TCGA-50-5049-01A-01D-1625-08 | TCGA-50-5049-10A-01D-1625-08 | g.chr21:40568393G>A | | | |
| LUAD | 21 | 40569067 | 40569067 | + | Missense_Mutation | SNP | C | C | G | TCGA-93-8067-01A-11D-2284-08 | TCGA-93-8067-10A-01D-2284-08 | g.chr21:40569067C>G | c.5928G>C | c.(5926-5928)ttG>ttC | p.L1976F |
| LUAD | 21 | 40569284 | 40569284 | + | Missense_Mutation | SNP | G | G | C | TCGA-49-4501-01A-01D-1265-08 | TCGA-49-4501-11A-01D-1265-08 | g.chr21:40569284G>C | c.5711C>G | c.(5710-5712)tCc>tGc | p.S1904C |
| LUAD | 21 | 40569301 | 40569301 | + | Silent | SNP | G | G | A | TCGA-78-8660-01A-11D-2393-08 | TCGA-78-8660-10A-01D-2393-08 | g.chr21:40569301G>A | c.5694C>T | c.(5692-5694)tcC>tcT | p.S1898S |
| LUAD | 21 | 40570870 | 40570870 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z023-01A-01W-0746-08 | TCGA-17-Z023-11A-01W-0746-08 | g.chr21:40570870G>C | c.5472C>G | c.(5470-5472)gaC>gaG | p.D1824E |
| LUAD | 21 | 40571250 | 40571250 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr21:40571250G>A | c.5092C>T | c.(5092-5094)Caa>Taa | p.Q1698* |
| LUAD | 21 | 40601363 | 40601363 | + | Splice_Site | SNP | C | C | A | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr21:40601363C>A | | c.e26-1 | |
| LUAD | 21 | 40604114 | 40604114 | + | Missense_Mutation | SNP | T | T | C | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr21:40604114T>C | c.2989A>G | c.(2989-2991)Atg>Gtg | p.M997V |
| LUAD | 21 | 40608649 | 40608649 | + | Missense_Mutation | SNP | A | A | C | TCGA-17-Z048-01A-01W-0746-08 | TCGA-17-Z048-11A-01W-0746-08 | g.chr21:40608649A>C | c.2638T>G | c.(2638-2640)Tta>Gta | p.L880V |
| LUAD | 21 | 40630520 | 40630520 | + | Missense_Mutation | SNP | A | A | G | TCGA-MP-A4TC-01A-11D-A24P-08 | TCGA-MP-A4TC-10A-01D-A24P-08 | g.chr21:40630520A>G | c.1964T>C | c.(1963-1965)cTt>cCt | p.L655P |
| LUSC | 21 | 40558971 | 40558971 | + | Missense_Mutation | SNP | C | C | A | TCGA-37-4133-01A-01D-1352-08 | TCGA-37-4133-10A-01D-1352-08 | g.chr21:40558971C>A | c.6944G>T | c.(6943-6945)tGg>tTg | p.W2315L |
| LUSC | 21 | 40559097 | 40559097 | + | Missense_Mutation | SNP | G | G | C | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr21:40559097G>C | c.6818C>G | c.(6817-6819)tCt>tGt | p.S2273C |
| LUSC | 21 | 40568985 | 40568985 | + | Missense_Mutation | SNP | C | C | T | TCGA-39-5031-01A-01D-1441-08 | TCGA-39-5031-11A-01D-1441-08 | g.chr21:40568985C>T | c.6010G>A | c.(6010-6012)Gaa>Aaa | p.E2004K |
| LUSC | 21 | 40570728 | 40570728 | + | Missense_Mutation | SNP | C | C | G | TCGA-39-5024-01A-21D-1817-08 | TCGA-39-5024-11A-01D-1817-08 | g.chr21:40570728C>G | c.5614G>C | c.(5614-5616)Gat>Cat | p.D1872H |
| LUSC | 21 | 40570785 | 40570785 | + | Missense_Mutation | SNP | G | G | T | TCGA-46-3765-01A-01D-0983-08 | TCGA-46-3765-10A-01D-0983-08 | g.chr21:40570785G>T | c.5557C>A | c.(5557-5559)Cct>Act | p.P1853T |
| LUSC | 21 | 40572204 | 40572204 | + | Missense_Mutation | SNP | C | C | A | TCGA-18-3410-01A-01D-0983-08 | TCGA-18-3410-11A-01D-0983-08 | g.chr21:40572204C>A | c.4694G>T | c.(4693-4695)gGg>gTg | p.G1565V |
| LUSC | 21 | 40582738 | 40582738 | + | Missense_Mutation | SNP | G | G | T | TCGA-33-4582-01A-01D-1441-08 | TCGA-33-4582-11A-01D-1441-08 | g.chr21:40582738G>T | c.4018C>A | c.(4018-4020)Caa>Aaa | p.Q1340K |
| LUSC | 21 | 40670440 | 40670440 | + | Missense_Mutation | SNP | C | C | A | TCGA-21-5782-01A-01D-1632-08 | TCGA-21-5782-10A-01D-1632-08 | g.chr21:40670440C>A | c.267G>T | c.(265-267)ttG>ttT | p.L89F |
| OV | 21 | 40584593 | 40584593 | + | Splice_Site | SNP | C | C | A | TCGA-29-2434-01A-01D-1526-09 | TCGA-29-2434-10A-01D-1526-09 | g.chr21:40584593C>A | c.3899G>T | c.(3898-3900)aGa>aTa | p.R1300I |
| OV | 21 | 40646359 | 40646359 | + | Missense_Mutation | SNP | C | C | A | TCGA-10-0930-01A-02W-0421-09 | TCGA-10-0930-11A-01W-0977-09 | g.chr21:40646359C>A | c.1185G>T | c.(1183-1185)tgG>tgT | p.W395C |
| OV | 21 | 40668205 | 40668205 | + | Missense_Mutation | SNP | G | G | A | TCGA-61-1899-01A-01W-0639-09 | TCGA-61-1899-11A-01W-0639-09 | g.chr21:40668205G>A | c.434C>T | c.(433-435)tCc>tTc | p.S145F |
| OV | 21 | 40670383 | 40670383 | + | Missense_Mutation | SNP | C | C | G | TCGA-59-2372-01A-01D-1526-09 | TCGA-59-2372-10A-01D-1526-09 | g.chr21:40670383C>G | c.324G>C | c.(322-324)agG>agC | p.R108S |
| PAAD | 21 | 40559106 | 40559106 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr21:40559106C>T | c.6809G>A | c.(6808-6810)cGa>cAa | p.R2270Q |
| PAAD | 21 | 40571514 | 40571514 | + | Missense_Mutation | SNP | T | T | A | TCGA-3A-A9I9-01A-11D-A38G-08 | TCGA-3A-A9I9-10A-01D-A38J-08 | g.chr21:40571514T>A | c.4828A>T | c.(4828-4830)Aat>Tat | p.N1610Y |
| PAAD | 21 | 40578075 | 40578075 | + | Silent | SNP | C | C | T | TCGA-3A-A9IO-01A-11D-A38G-08 | TCGA-3A-A9IO-10A-01D-A38J-08 | g.chr21:40578075C>T | c.4323G>A | c.(4321-4323)cgG>cgA | p.R1441R |
| PAAD | 21 | 40578076 | 40578076 | + | Missense_Mutation | SNP | C | C | A | TCGA-HZ-A77Q-01A-11D-A36O-08 | TCGA-HZ-A77Q-10A-01D-A367-08 | g.chr21:40578076C>A | c.4322G>T | c.(4321-4323)cGg>cTg | p.R1441L |
| PAAD | 21 | 40578077 | 40578077 | + | Missense_Mutation | SNP | G | G | A | TCGA-2J-AAB1-01A-11D-A40W-08 | TCGA-2J-AAB1-10A-01D-A40W-08 | g.chr21:40578077G>A | c.4321C>T | c.(4321-4323)Cgg>Tgg | p.R1441W |
| PAAD | 21 | 40582011 | 40582011 | + | Silent | SNP | C | C | A | TCGA-XN-A8T3-01A-11D-A36O-08 | TCGA-XN-A8T3-10A-01D-A367-08 | g.chr21:40582011C>A | c.4107G>T | c.(4105-4107)gcG>gcT | p.A1369A |
| PAAD | 21 | 40604155 | 40604155 | + | Missense_Mutation | SNP | T | T | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr21:40604155T>G | c.2948A>C | c.(2947-2949)aAt>aCt | p.N983T |
| PAAD | 21 | 40630429 | 40630429 | + | Silent | SNP | T | T | C | TCGA-Q3-A5QY-01A-12D-A32N-08 | TCGA-Q3-A5QY-10A-01D-A32N-08 | g.chr21:40630429T>C | c.2055A>G | c.(2053-2055)gaA>gaG | p.E685E |
| PAAD | 21 | 40646333 | 40646333 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr21:40646333C>T | c.1211G>A | c.(1210-1212)aGc>aAc | p.S404N |
| PAAD | 21 | 40650700 | 40650700 | + | Silent | SNP | G | G | A | TCGA-HZ-A49I-01A-12D-A26I-08 | TCGA-HZ-A49I-10A-01D-A26I-08 | g.chr21:40650700G>A | c.972C>T | c.(970-972)ggC>ggT | p.G324G |
| PRAD | 21 | 40568702 | 40568702 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr21:40568702C>T | c.6293G>A | c.(6292-6294)gGc>gAc | p.G2098D |
| PRAD | 21 | 40571323 | 40571324 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr21:40571323_40571324insT | c.5018_5019insA | c.(5017-5019)aagfs | p.K1673fs |
| PRAD | 21 | 40582837 | 40582837 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr21:40582837delT | c.3919delA | c.(3919-3921)agcfs | p.S1307fs |
| PRAD | 21 | 40584626 | 40584626 | + | Missense_Mutation | SNP | C | C | A | TCGA-HC-A9TE-01A-11D-A41K-08 | TCGA-HC-A9TE-10A-01D-A41N-08 | g.chr21:40584626C>A | c.3866G>T | c.(3865-3867)aGt>aTt | p.S1289I |
| PRAD | 21 | 40596364 | 40596364 | + | Missense_Mutation | SNP | G | G | A | TCGA-KK-A7B3-01A-11D-A33T-08 | TCGA-KK-A7B3-11A-21D-A33W-08 | g.chr21:40596364G>A | c.3352C>T | c.(3352-3354)Cca>Tca | p.P1118S |
| PRAD | 21 | 40668227 | 40668227 | + | Missense_Mutation | SNP | C | C | T | TCGA-HC-7744-01A-11D-2114-08 | TCGA-HC-7744-10A-01D-2115-08 | g.chr21:40668227C>T | c.412G>A | c.(412-414)Gaa>Aaa | p.E138K |
| READ | 21 | 40559097 | 40559097 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr21:40559097G>T | c.6818C>A | c.(6817-6819)tCt>tAt | p.S2273Y |
| READ | 21 | 40568294 | 40568294 | + | Intron | SNP | C | C | T | TCGA-DC-6682-01A-11D-1826-10 | TCGA-DC-6682-10A-01D-1826-10 | g.chr21:40568294C>T | | | |
| READ | 21 | 40570895 | 40570895 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr21:40570895G>T | c.5447C>A | c.(5446-5448)aCc>aAc | p.T1816N |
| READ | 21 | 40578199 | 40578199 | + | Splice_Site | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr21:40578199A>C | c.4199T>G | c.(4198-4200)aTt>aGt | p.I1400S |
| READ | 21 | 40587276 | 40587276 | + | Silent | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr21:40587276C>T | c.3672G>A | c.(3670-3672)gcG>gcA | p.A1224A |
| READ | 21 | 40610476 | 40610476 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A01Y-01A-41W-A096-10 | TCGA-AG-A01Y-11A-11W-A096-10 | g.chr21:40610476T>G | c.2505A>C | c.(2503-2505)gaA>gaC | p.E835D |
| SKCM | 21 | 40568855 | 40568855 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr21:40568855G>A | c.6140C>T | c.(6139-6141)tCc>tTc | p.S2047F |
| SKCM | 21 | 40571405 | 40571405 | + | Missense_Mutation | SNP | A | A | G | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr21:40571405A>G | c.4937T>C | c.(4936-4938)gTa>gCa | p.V1646A |
| SKCM | 21 | 40571568 | 40571568 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr21:40571568C>T | c.4774G>A | c.(4774-4776)Gga>Aga | p.G1592R |
| SKCM | 21 | 40572226 | 40572226 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr21:40572226G>A | c.4672C>T | c.(4672-4674)Cgt>Tgt | p.R1558C |
| SKCM | 21 | 40574327 | 40574327 | + | Silent | SNP | A | A | G | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr21:40574327A>G | c.4509T>C | c.(4507-4509)ggT>ggC | p.G1503G |
| SKCM | 21 | 40574346 | 40574346 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr21:40574346G>A | c.4490C>T | c.(4489-4491)tCt>tTt | p.S1497F |
| SKCM | 21 | 40581929 | 40581929 | + | Silent | SNP | T | T | G | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr21:40581929T>G | c.4189A>C | c.(4189-4191)Aga>Cga | p.R1397R |
| SKCM | 21 | 40587164 | 40587164 | + | Splice_Site | SNP | T | T | C | TCGA-D3-A1QB-06A-11D-A19A-08 | TCGA-D3-A1QB-10A-01D-A19A-08 | g.chr21:40587164T>C | c.3784A>G | c.(3784-3786)Aag>Gag | p.K1262E |
| SKCM | 21 | 40590094 | 40590094 | + | Missense_Mutation | SNP | C | C | G | TCGA-EE-A2A0-06A-11D-A196-08 | TCGA-EE-A2A0-10A-01D-A198-08 | g.chr21:40590094C>G | c.3643G>C | c.(3643-3645)Gtt>Ctt | p.V1215L |
| SKCM | 21 | 40590106 | 40590106 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr21:40590106G>A | c.3631C>T | c.(3631-3633)Cga>Tga | p.R1211* |
| SKCM | 21 | 40590178 | 40590178 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr21:40590178C>T | c.3559G>A | c.(3559-3561)Ggc>Agc | p.G1187S |
| SKCM | 21 | 40597051 | 40597051 | + | Missense_Mutation | SNP | G | G | T | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr21:40597051G>T | c.3281C>A | c.(3280-3282)cCa>cAa | p.P1094Q |
| SKCM | 21 | 40601257 | 40601257 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A198-06A-11D-A196-08 | TCGA-ER-A198-10A-01D-A198-08 | g.chr21:40601257C>T | c.3106G>A | c.(3106-3108)Gac>Aac | p.D1036N |
| SKCM | 21 | 40627740 | 40627740 | + | Missense_Mutation | SNP | T | T | G | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr21:40627740T>G | c.2086A>C | c.(2086-2088)Agc>Cgc | p.S696R |
| SKCM | 21 | 40642347 | 40642347 | + | Silent | SNP | G | G | A | TCGA-D9-A3Z1-06A-11D-A23B-08 | TCGA-D9-A3Z1-10A-01D-A23B-08 | g.chr21:40642347G>A | c.1257C>T | c.(1255-1257)tcC>tcT | p.S419S |
| SKCM | 21 | 40642348 | 40642348 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A3Z1-06A-11D-A23B-08 | TCGA-D9-A3Z1-10A-01D-A23B-08 | g.chr21:40642348G>A | c.1256C>T | c.(1255-1257)tCc>tTc | p.S419F |
| SKCM | 21 | 40646331 | 40646331 | + | Missense_Mutation | SNP | T | T | A | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr21:40646331T>A | c.1213A>T | c.(1213-1215)Att>Ttt | p.I405F |
| SKCM | 21 | 40648100 | 40648100 | + | Splice_Site | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr21:40648100G>A | c.1144C>T | c.(1144-1146)Cgg>Tgg | p.R382W |
| SKCM | 21 | 40649245 | 40649245 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr21:40649245G>A | c.1036C>T | c.(1036-1038)Cat>Tat | p.H346Y |
| SKCM | 21 | 40652086 | 40652086 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr21:40652086G>A | c.920C>T | c.(919-921)tCc>tTc | p.S307F |
| SKCM | 21 | 40652152 | 40652152 | + | Missense_Mutation | SNP | G | G | C | TCGA-EE-A2GT-06A-12D-A197-08 | TCGA-EE-A2GT-10A-01D-A199-08 | g.chr21:40652152G>C | c.854C>G | c.(853-855)tCt>tGt | p.S285C |
| SKCM | 21 | 40665885 | 40665885 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr21:40665885G>A | c.683C>T | c.(682-684)tCt>tTt | p.S228F |
| SKCM | 21 | 40670378 | 40670378 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr21:40670378G>A | c.329C>T | c.(328-330)tCt>tTt | p.S110F |