| 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 |
| BLCA | 10 | 21097558 | 21097558 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chr10:21097558G>C | c.2642C>G | c.(2641-2643)tCt>tGt | p.S881C |
| BLCA | 10 | 21097571 | 21097571 | + | Missense_Mutation | SNP | T | T | C | TCGA-UY-A78N-01A-12D-A339-08 | TCGA-UY-A78N-10A-01D-A339-08 | g.chr10:21097571T>C | c.2629A>G | c.(2629-2631)Agg>Ggg | p.R877G |
| BLCA | 10 | 21098812 | 21098812 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr10:21098812C>T | c.2534G>A | c.(2533-2535)cGc>cAc | p.R845H |
| BLCA | 10 | 21101749 | 21101749 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A5BZ-01A-11D-A289-08 | TCGA-FD-A5BZ-10A-01D-A289-08 | g.chr10:21101749C>G | c.2467G>C | c.(2467-2469)Ggg>Cgg | p.G823R |
| BLCA | 10 | 21102872 | 21102872 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-CU-A3KJ-01A-11D-A21A-08 | TCGA-CU-A3KJ-10A-01D-A21A-08 | g.chr10:21102872G>C | c.2342C>G | c.(2341-2343)tCa>tGa | p.S781* |
| BLCA | 10 | 21104628 | 21104628 | + | Missense_Mutation | SNP | G | G | T | TCGA-FD-A6TH-01A-11D-A32B-08 | TCGA-FD-A6TH-10A-01D-A329-08 | g.chr10:21104628G>T | c.2167C>A | c.(2167-2169)Ctg>Atg | p.L723M |
| BLCA | 10 | 21117520 | 21117520 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A1AB-01A-11D-A13W-08 | TCGA-DK-A1AB-10A-01D-A13W-08 | g.chr10:21117520G>A | c.1715C>T | c.(1714-1716)tCt>tTt | p.S572F |
| BLCA | 10 | 21117535 | 21117535 | + | Missense_Mutation | SNP | A | A | G | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chr10:21117535A>G | c.1700T>C | c.(1699-1701)aTg>aCg | p.M567T |
| BLCA | 10 | 21120438 | 21120438 | + | Silent | SNP | G | G | A | TCGA-S5-AA26-01A-11D-A38G-08 | TCGA-S5-AA26-10A-01D-A38J-08 | g.chr10:21120438G>A | c.1524C>T | c.(1522-1524)gtC>gtT | p.V508V |
| BLCA | 10 | 21139390 | 21139390 | + | Silent | SNP | T | T | A | TCGA-XF-A9T3-01A-11D-A42E-08 | TCGA-XF-A9T3-10A-01D-A42H-08 | g.chr10:21139390T>A | c.1050A>T | c.(1048-1050)ccA>ccT | p.P350P |
| BLCA | 10 | 21158753 | 21158753 | + | Silent | SNP | G | G | A | TCGA-E5-A4TZ-01A-11D-A31L-08 | TCGA-E5-A4TZ-10B-01D-A31J-08 | g.chr10:21158753G>A | c.498C>T | c.(496-498)gaC>gaT | p.D166D |
| BLCA | 10 | 21178818 | 21178818 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr10:21178818G>C | c.214C>G | c.(214-216)Cct>Gct | p.P72A |
| BLCA | 10 | 21462717 | 21462717 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-G2-AA3B-01A-11D-A391-08 | TCGA-G2-AA3B-10A-01D-A394-08 | g.chr10:21462717C>A | c.46G>T | c.(46-48)Gag>Tag | p.E16* |
| BRCA | 10 | 21097452 | 21097452 | + | Silent | SNP | C | C | T | TCGA-EW-A1IZ-01A-11D-A188-09 | TCGA-EW-A1IZ-10A-01D-A13O-09 | g.chr10:21097452C>T | c.2748G>A | c.(2746-2748)ccG>ccA | p.P916P |
| BRCA | 10 | 21097581 | 21097581 | + | Silent | SNP | C | C | A | TCGA-E2-A14R-01A-11D-A10Y-09 | TCGA-E2-A14R-10A-01D-A110-09 | g.chr10:21097581C>A | c.2619G>T | c.(2617-2619)gcG>gcT | p.A873A |
| BRCA | 10 | 21134276 | 21134276 | + | Missense_Mutation | SNP | C | C | G | TCGA-BH-A18P-01A-11D-A12B-09 | TCGA-BH-A18P-11A-43D-A12B-09 | g.chr10:21134276C>G | c.1138G>C | c.(1138-1140)Gag>Cag | p.E380Q |
| BRCA | 10 | 21157693 | 21157693 | + | Splice_Site | SNP | G | G | T | TCGA-BH-A0BP-01A-11D-A10Y-09 | TCGA-BH-A0BP-10A-01D-A110-09 | g.chr10:21157693G>T | c.584C>A | c.(583-585)gCa>gAa | p.A195E |
| BRCA | 10 | 21177025 | 21177025 | + | Splice_Site | SNP | C | C | A | TCGA-D8-A1JD-01A-11D-A13L-09 | TCGA-D8-A1JD-10A-01D-A13O-09 | g.chr10:21177025C>A | | c.e4+1 | |
| BRCA | 10 | 21186081 | 21186081 | + | Missense_Mutation | SNP | T | T | C | TCGA-AN-A0AM-01A-11W-A050-09 | TCGA-AN-A0AM-10A-01W-A055-09 | g.chr10:21186081T>C | c.54A>G | c.(52-54)atA>atG | p.I18M |
| BRCA | 10 | 21186095 | 21186095 | + | Missense_Mutation | SNP | C | C | T | TCGA-C8-A1HM-01A-12D-A135-09 | TCGA-C8-A1HM-10A-01D-A135-09 | g.chr10:21186095C>T | c.40G>A | c.(40-42)Gaa>Aaa | p.E14K |
| CESC | 10 | 21097533 | 21097533 | + | Silent | SNP | G | G | A | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr10:21097533G>A | c.2667C>T | c.(2665-2667)ttC>ttT | p.F889F |
| CESC | 10 | 21098823 | 21098823 | + | Silent | SNP | G | G | A | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr10:21098823G>A | c.2523C>T | c.(2521-2523)ctC>ctT | p.L841L |
| CESC | 10 | 21115385 | 21115385 | + | Silent | SNP | A | A | G | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chr10:21115385A>G | c.1860T>C | c.(1858-1860)aaT>aaC | p.N620N |
| CESC | 10 | 21141488 | 21141488 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A7UE-01A-11D-A33O-09 | TCGA-C5-A7UE-10A-01D-A33O-09 | g.chr10:21141488C>T | c.994G>A | c.(994-996)Gtc>Atc | p.V332I |
| CHOL | 10 | 21169808 | 21169808 | + | Missense_Mutation | SNP | G | G | T | TCGA-W5-AA2T-01A-12D-A417-09 | TCGA-W5-AA2T-10A-01D-A41A-09 | g.chr10:21169808G>T | c.395C>A | c.(394-396)gCt>gAt | p.A132D |
| COAD | 10 | 21074741 | 21074741 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-5254-01A-21D-1835-10 | TCGA-CA-5254-10A-01D-1835-10 | g.chr10:21074741C>T | c.2980G>A | c.(2980-2982)Ggc>Agc | p.G994S |
| COAD | 10 | 21074778 | 21074778 | + | Silent | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr10:21074778G>A | c.2943C>T | c.(2941-2943)atC>atT | p.I981I |
| COAD | 10 | 21074832 | 21074832 | + | Silent | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr10:21074832G>A | c.2889C>T | c.(2887-2889)taC>taT | p.Y963Y |
| COAD | 10 | 21097467 | 21097467 | + | Silent | SNP | A | A | G | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr10:21097467A>G | c.2733T>C | c.(2731-2733)agT>agC | p.S911S |
| COAD | 10 | 21098790 | 21098790 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr10:21098790G>A | c.2556C>T | c.(2554-2556)ttC>ttT | p.F852F |
| COAD | 10 | 21101810 | 21101810 | + | Silent | SNP | G | G | A | TCGA-CA-5254-01A-21D-1835-10 | TCGA-CA-5254-10A-01D-1835-10 | g.chr10:21101810G>A | c.2406C>T | c.(2404-2406)gaC>gaT | p.D802D |
| COAD | 10 | 21101810 | 21101810 | + | Silent | SNP | G | G | A | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr10:21101810G>A | c.2406C>T | c.(2404-2406)gaC>gaT | p.D802D |
| COAD | 10 | 21108382 | 21108383 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr10:21108382_21108383delCT | c.2025_2026delAG | c.(2023-2028)agagtgfs | p.RV675fs |
| COAD | 10 | 21115407 | 21115407 | + | Missense_Mutation | SNP | C | C | T | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr10:21115407C>T | c.1838G>A | c.(1837-1839)cGa>cAa | p.R613Q |
| COAD | 10 | 21124457 | 21124457 | + | Silent | SNP | T | T | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr10:21124457T>A | c.1434A>T | c.(1432-1434)gcA>gcT | p.A478A |
| COAD | 10 | 21129730 | 21129730 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-DM-A285-01A-11D-A16V-10 | TCGA-DM-A285-10A-01D-A16V-10 | g.chr10:21129730C>A | c.1276G>T | c.(1276-1278)Gaa>Taa | p.E426* |
| COAD | 10 | 21139325 | 21139325 | + | Splice_Site | SNP | T | T | C | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr10:21139325T>C | c.1115A>G | c.(1114-1116)gAa>gGa | p.E372G |
| COAD | 10 | 21147173 | 21147173 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr10:21147173C>T | c.899G>A | c.(898-900)aGc>aAc | p.S300N |
| COAD | 10 | 21178869 | 21178869 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr10:21178869T>C | c.163A>G | c.(163-165)Aaa>Gaa | p.K55E |
| COAD | 10 | 21186104 | 21186104 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr10:21186104C>A | c.31G>T | c.(31-33)Gat>Tat | p.D11Y |
| COAD | 10 | 21250693 | 21250693 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr10:21250693C>T | c.265G>A | c.(265-267)Gat>Aat | p.D89N |
| COAD | 10 | 21461365 | 21461365 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-5657-01A-01D-1650-10 | TCGA-A6-5657-10A-01D-1650-10 | g.chr10:21461365C>A | c.111G>T | c.(109-111)atG>atT | p.M37I |
| COADREAD | 10 | 21074741 | 21074741 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-5254-01A-21D-1835-10 | TCGA-CA-5254-10A-01D-1835-10 | g.chr10:21074741C>T | c.2980G>A | c.(2980-2982)Ggc>Agc | p.G994S |
| COADREAD | 10 | 21074778 | 21074778 | + | Silent | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr10:21074778G>A | c.2943C>T | c.(2941-2943)atC>atT | p.I981I |
| COADREAD | 10 | 21074816 | 21074816 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr10:21074816C>T | c.2905G>A | c.(2905-2907)Gat>Aat | p.D969N |
| COADREAD | 10 | 21074832 | 21074832 | + | Silent | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr10:21074832G>A | c.2889C>T | c.(2887-2889)taC>taT | p.Y963Y |
| COADREAD | 10 | 21097467 | 21097467 | + | Silent | SNP | A | A | G | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr10:21097467A>G | c.2733T>C | c.(2731-2733)agT>agC | p.S911S |
| COADREAD | 10 | 21098789 | 21098789 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:21098789C>T | c.2557G>A | c.(2557-2559)Gac>Aac | p.D853N |
| COADREAD | 10 | 21098790 | 21098790 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr10:21098790G>A | c.2556C>T | c.(2554-2556)ttC>ttT | p.F852F |
| COADREAD | 10 | 21101810 | 21101810 | + | Silent | SNP | G | G | A | TCGA-CA-5254-01A-21D-1835-10 | TCGA-CA-5254-10A-01D-1835-10 | g.chr10:21101810G>A | c.2406C>T | c.(2404-2406)gaC>gaT | p.D802D |
| COADREAD | 10 | 21101810 | 21101810 | + | Silent | SNP | G | G | A | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr10:21101810G>A | c.2406C>T | c.(2404-2406)gaC>gaT | p.D802D |
| COADREAD | 10 | 21108382 | 21108383 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr10:21108382_21108383delCT | c.2025_2026delAG | c.(2023-2028)agagtgfs | p.RV675fs |
| COADREAD | 10 | 21115407 | 21115407 | + | Missense_Mutation | SNP | C | C | T | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr10:21115407C>T | c.1838G>A | c.(1837-1839)cGa>cAa | p.R613Q |
| COADREAD | 10 | 21124457 | 21124457 | + | Silent | SNP | T | T | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr10:21124457T>A | c.1434A>T | c.(1432-1434)gcA>gcT | p.A478A |
| COADREAD | 10 | 21124510 | 21124510 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr10:21124510C>A | c.1381G>T | c.(1381-1383)Gga>Tga | p.G461* |
| COADREAD | 10 | 21129730 | 21129730 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-DM-A285-01A-11D-A16V-10 | TCGA-DM-A285-10A-01D-A16V-10 | g.chr10:21129730C>A | c.1276G>T | c.(1276-1278)Gaa>Taa | p.E426* |
| COADREAD | 10 | 21139325 | 21139325 | + | Splice_Site | SNP | T | T | C | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr10:21139325T>C | c.1115A>G | c.(1114-1116)gAa>gGa | p.E372G |
| COADREAD | 10 | 21139426 | 21139426 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:21139426T>G | c.1014A>C | c.(1012-1014)aaA>aaC | p.K338N |
| COADREAD | 10 | 21147173 | 21147173 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr10:21147173C>T | c.899G>A | c.(898-900)aGc>aAc | p.S300N |
| COADREAD | 10 | 21177028 | 21177028 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:21177028C>A | c.367G>T | c.(367-369)Gag>Tag | p.E123* |
| COADREAD | 10 | 21178869 | 21178869 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr10:21178869T>C | c.163A>G | c.(163-165)Aaa>Gaa | p.K55E |
| COADREAD | 10 | 21186104 | 21186104 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr10:21186104C>A | c.31G>T | c.(31-33)Gat>Tat | p.D11Y |
| COADREAD | 10 | 21250693 | 21250693 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr10:21250693C>T | c.265G>A | c.(265-267)Gat>Aat | p.D89N |
| COADREAD | 10 | 21461365 | 21461365 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-5657-01A-01D-1650-10 | TCGA-A6-5657-10A-01D-1650-10 | g.chr10:21461365C>A | c.111G>T | c.(109-111)atG>atT | p.M37I |
| DLBC | 10 | 21309077 | 21309077 | + | Missense_Mutation | SNP | C | C | T | TCGA-FA-A6HO-01A-11D-A31X-10 | TCGA-FA-A6HO-10A-01D-A31X-10 | g.chr10:21309077C>T | c.218G>A | c.(217-219)cGc>cAc | p.R73H |
| DLBC | 10 | 21309114 | 21309114 | + | Missense_Mutation | SNP | A | A | G | TCGA-GS-A9TW-01A-11D-A382-10 | TCGA-GS-A9TW-10A-01D-A385-10 | g.chr10:21309114A>G | c.181T>C | c.(181-183)Tcc>Ccc | p.S61P |
| ESCA | 10 | 21076223 | 21076223 | + | Missense_Mutation | SNP | C | C | T | TCGA-2H-A9GR-01A-12D-A37C-09 | TCGA-2H-A9GR-11A-11D-A37F-09 | g.chr10:21076223C>T | c.2776G>A | c.(2776-2778)Gga>Aga | p.G926R |
| ESCA | 10 | 21097518 | 21097518 | + | Silent | SNP | T | T | A | TCGA-JY-A6FA-01A-11D-A33E-09 | TCGA-JY-A6FA-10A-01D-A33H-09 | g.chr10:21097518T>A | c.2682A>T | c.(2680-2682)ggA>ggT | p.G894G |
| ESCA | 10 | 21108359 | 21108359 | + | Silent | SNP | C | C | T | TCGA-IG-A3I8-01A-11D-A247-09 | TCGA-IG-A3I8-10A-01D-A247-09 | g.chr10:21108359C>T | c.2049G>A | c.(2047-2049)ctG>ctA | p.L683L |
| ESCA | 10 | 21112176 | 21112176 | + | Silent | SNP | T | T | C | TCGA-R6-A8WG-01A-11D-A37C-09 | TCGA-R6-A8WG-10A-01D-A37F-09 | g.chr10:21112176T>C | c.1923A>G | c.(1921-1923)gaA>gaG | p.E641E |
| ESCA | 10 | 21250693 | 21250693 | + | Missense_Mutation | SNP | C | C | A | TCGA-L7-A6VZ-01A-12D-A33E-09 | TCGA-L7-A6VZ-10A-01D-A33H-09 | g.chr10:21250693C>A | c.265G>T | c.(265-267)Gat>Tat | p.D89Y |
| GBM | 10 | 21112168 | 21112168 | + | Missense_Mutation | SNP | C | C | T | TCGA-76-4929-01A-01D-1486-08 | TCGA-76-4929-10A-01D-1486-08 | g.chr10:21112168C>T | c.1931G>A | c.(1930-1932)aGa>aAa | p.R644K |
| GBM | 10 | 21120216 | 21120216 | + | Missense_Mutation | SNP | A | A | G | TCGA-28-5213-01A-01D-1486-08 | TCGA-28-5213-10A-01D-1486-08 | g.chr10:21120216A>G | c.1580T>C | c.(1579-1581)tTa>tCa | p.L527S |
| GBM | 10 | 21124444 | 21124444 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-28-5207-01A-01D-1486-08 | TCGA-28-5207-10A-01D-1486-08 | g.chr10:21124444C>A | c.1447G>T | c.(1447-1449)Gag>Tag | p.E483* |
| GBM | 10 | 21185902 | 21185902 | + | Silent | SNP | C | C | T | TCGA-41-6646-01A-11D-1845-08 | TCGA-41-6646-10A-01D-1845-08 | g.chr10:21185902C>T | c.138G>A | c.(136-138)acG>acA | p.T46T |
| GBM | 10 | 21461321 | 21461321 | + | Missense_Mutation | SNP | T | T | C | TCGA-02-2470-01A-01D-1494-08 | TCGA-02-2470-10A-01D-1494-08 | g.chr10:21461321T>C | c.155A>G | c.(154-156)tAt>tGt | p.Y52C |
| GBMLGG | 10 | 21074807 | 21074807 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A7TI-01A-11D-A33T-08 | TCGA-DU-A7TI-10A-01D-A33W-08 | g.chr10:21074807C>T | c.2914G>A | c.(2914-2916)Gag>Aag | p.E972K |
| GBMLGG | 10 | 21074810 | 21074810 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:21074810C>A | c.2911G>T | c.(2911-2913)Gac>Tac | p.D971Y |
| GBMLGG | 10 | 21097453 | 21097453 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-8168-01A-11D-2253-08 | TCGA-DU-8168-10A-01D-2253-08 | g.chr10:21097453G>A | c.2747C>T | c.(2746-2748)cCg>cTg | p.P916L |
| GBMLGG | 10 | 21097515 | 21097515 | + | Silent | SNP | G | G | A | TCGA-E1-5304-01A-01D-1468-08 | TCGA-E1-5304-10A-01D-1468-08 | g.chr10:21097515G>A | c.2685C>T | c.(2683-2685)gaC>gaT | p.D895D |
| GBMLGG | 10 | 21098829 | 21098829 | + | Splice_Site | SNP | T | T | C | TCGA-FG-A87N-01A-11D-A36O-08 | TCGA-FG-A87N-10A-01D-A367-08 | g.chr10:21098829T>C | | c.e25-2 | |
| GBMLGG | 10 | 21101818 | 21101818 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:21101818C>T | c.2398G>A | c.(2398-2400)Gtc>Atc | p.V800I |
| GBMLGG | 10 | 21112168 | 21112168 | + | Missense_Mutation | SNP | C | C | T | TCGA-76-4929-01A-01D-1486-08 | TCGA-76-4929-10A-01D-1486-08 | g.chr10:21112168C>T | c.1931G>A | c.(1930-1932)aGa>aAa | p.R644K |
| GBMLGG | 10 | 21120204 | 21120204 | + | Missense_Mutation | SNP | A | A | C | TCGA-E1-A7YK-01A-11D-A34A-08 | TCGA-E1-A7YK-10A-01D-A34A-08 | g.chr10:21120204A>C | c.1592T>G | c.(1591-1593)aTt>aGt | p.I531S |
| GBMLGG | 10 | 21120216 | 21120216 | + | Missense_Mutation | SNP | A | A | G | TCGA-28-5213-01A-01D-1486-08 | TCGA-28-5213-10A-01D-1486-08 | g.chr10:21120216A>G | c.1580T>C | c.(1579-1581)tTa>tCa | p.L527S |
| GBMLGG | 10 | 21120450 | 21120450 | + | Missense_Mutation | SNP | G | G | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:21120450G>C | c.1512C>G | c.(1510-1512)gaC>gaG | p.D504E |
| GBMLGG | 10 | 21124444 | 21124444 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-28-5207-01A-01D-1486-08 | TCGA-28-5207-10A-01D-1486-08 | g.chr10:21124444C>A | c.1447G>T | c.(1447-1449)Gag>Tag | p.E483* |
| GBMLGG | 10 | 21139359 | 21139359 | + | Missense_Mutation | SNP | G | G | C | TCGA-DU-A7TA-01A-11D-A33T-08 | TCGA-DU-A7TA-10A-01D-A33W-08 | g.chr10:21139359G>C | c.1081C>G | c.(1081-1083)Caa>Gaa | p.Q361E |
| GBMLGG | 10 | 21185902 | 21185902 | + | Silent | SNP | C | C | T | TCGA-41-6646-01A-11D-1845-08 | TCGA-41-6646-10A-01D-1845-08 | g.chr10:21185902C>T | c.138G>A | c.(136-138)acG>acA | p.T46T |
| GBMLGG | 10 | 21185916 | 21185916 | + | Missense_Mutation | SNP | C | C | A | TCGA-E1-A7YI-01A-11D-A34A-08 | TCGA-E1-A7YI-10A-01D-A34A-08 | g.chr10:21185916C>A | c.124G>T | c.(124-126)Gcc>Tcc | p.A42S |
| GBMLGG | 10 | 21461321 | 21461321 | + | Missense_Mutation | SNP | T | T | C | TCGA-02-2470-01A-01D-1494-08 | TCGA-02-2470-10A-01D-1494-08 | g.chr10:21461321T>C | c.155A>G | c.(154-156)tAt>tGt | p.Y52C |
| GBMLGG | 10 | 21462709 | 21462709 | + | Silent | SNP | G | G | A | TCGA-VW-A8FI-01A-11D-A36O-08 | TCGA-VW-A8FI-10A-01D-A367-08 | g.chr10:21462709G>A | c.54C>T | c.(52-54)gtC>gtT | p.V18V |
| HNSC | 10 | 21097456 | 21097456 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr10:21097456C>T | c.2744G>A | c.(2743-2745)aGa>aAa | p.R915K |
| HNSC | 10 | 21097543 | 21097543 | + | Missense_Mutation | SNP | C | C | G | TCGA-F7-A50J-01A-21D-A28R-08 | TCGA-F7-A50J-10A-01D-A28U-08 | g.chr10:21097543C>G | c.2657G>C | c.(2656-2658)aGc>aCc | p.S886T |
| HNSC | 10 | 21098748 | 21098748 | + | Silent | SNP | G | G | C | TCGA-T2-A6WX-01A-12D-A34J-08 | TCGA-T2-A6WX-10B-01D-A34M-08 | g.chr10:21098748G>C | c.2598C>G | c.(2596-2598)ctC>ctG | p.L866L |
| HNSC | 10 | 21106596 | 21106596 | + | Missense_Mutation | SNP | C | C | T | TCGA-IQ-7630-01A-11D-2078-08 | TCGA-IQ-7630-10A-01D-2078-08 | g.chr10:21106596C>T | c.2081G>A | c.(2080-2082)cGg>cAg | p.R694Q |
| HNSC | 10 | 21108395 | 21108395 | + | Silent | SNP | C | C | T | TCGA-CN-A63T-01A-11D-A28R-08 | TCGA-CN-A63T-10A-01D-A28U-08 | g.chr10:21108395C>T | c.2013G>A | c.(2011-2013)ccG>ccA | p.P671P |
| HNSC | 10 | 21108419 | 21108419 | + | Silent | SNP | C | C | T | TCGA-CR-7402-01A-11D-2012-08 | TCGA-CR-7402-10A-01D-2013-08 | g.chr10:21108419C>T | c.1989G>A | c.(1987-1989)aaG>aaA | p.K663K |
| HNSC | 10 | 21117520 | 21117520 | + | Missense_Mutation | SNP | G | G | C | TCGA-KU-A6H7-01A-11D-A31L-08 | TCGA-KU-A6H7-10A-01D-A31J-08 | g.chr10:21117520G>C | c.1715C>G | c.(1714-1716)tCt>tGt | p.S572C |
| HNSC | 10 | 21139422 | 21139422 | + | Missense_Mutation | SNP | T | T | C | TCGA-CN-5356-01A-01D-1434-08 | TCGA-CN-5356-10A-01D-1434-08 | g.chr10:21139422T>C | c.1018A>G | c.(1018-1020)Aaa>Gaa | p.K340E |
| HNSC | 10 | 21139430 | 21139430 | + | Splice_Site | SNP | A | A | G | TCGA-CR-7374-01A-11D-2012-08 | TCGA-CR-7374-10A-01D-2013-08 | g.chr10:21139430A>G | c.1010T>C | c.(1009-1011)gTg>gCg | p.V337A |
| HNSC | 10 | 21141477 | 21141477 | + | Missense_Mutation | SNP | A | A | T | TCGA-UF-A71D-01A-12D-A34J-08 | TCGA-UF-A71D-10B-01D-A34M-08 | g.chr10:21141477A>T | c.1005T>A | c.(1003-1005)agT>agA | p.S335R |
| HNSC | 10 | 21141501 | 21141501 | + | Silent | SNP | A | A | G | TCGA-QK-A6VB-01A-12D-A34J-08 | TCGA-QK-A6VB-10B-01D-A34M-08 | g.chr10:21141501A>G | c.981T>C | c.(979-981)caT>caC | p.H327H |
| HNSC | 10 | 21178840 | 21178845 | + | In_Frame_Del | DEL | CTTATC | CTTATC | - | TCGA-P3-A6T4-01A-11D-A34J-08 | TCGA-P3-A6T4-10A-01D-A34M-08 | g.chr10:21178840_21178845delCTTATC | c.187_192delGATAAG | c.(187-192)gataagdel | p.DK63del |
| KICH | 10 | 21097515 | 21097515 | + | Silent | SNP | G | G | A | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr10:21097515G>A | c.2685C>T | c.(2683-2685)gaC>gaT | p.D895D |
| KIPAN | 10 | 21076186 | 21076186 | + | Missense_Mutation | SNP | T | T | C | TCGA-A3-3357-01A-02D-1421-08 | TCGA-A3-3357-11A-01D-1421-08 | g.chr10:21076186T>C | c.2813A>G | c.(2812-2814)tAc>tGc | p.Y938C |
| KIPAN | 10 | 21097515 | 21097515 | + | Silent | SNP | G | G | A | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr10:21097515G>A | c.2685C>T | c.(2683-2685)gaC>gaT | p.D895D |
| KIPAN | 10 | 21124510 | 21124510 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CJ-6027-01A-11D-1669-08 | TCGA-CJ-6027-11A-01D-1669-08 | g.chr10:21124510C>A | c.1381G>T | c.(1381-1383)Gga>Tga | p.G461* |
| KIPAN | 10 | 21158725 | 21158725 | + | Missense_Mutation | SNP | C | C | G | TCGA-B2-5635-01A-01D-1534-10 | TCGA-B2-5635-10A-01D-1535-10 | g.chr10:21158725C>G | c.526G>C | c.(526-528)Gaa>Caa | p.E176Q |
| KIPAN | 10 | 21309109 | 21309109 | + | Silent | SNP | G | G | A | TCGA-B3-4104-01A-01D-1458-08 | TCGA-B3-4104-10A-01D-1458-08 | g.chr10:21309109G>A | c.186C>T | c.(184-186)ttC>ttT | p.F62F |
| KIRC | 10 | 21076186 | 21076186 | + | Missense_Mutation | SNP | T | T | C | TCGA-A3-3357-01A-02D-1421-08 | TCGA-A3-3357-11A-01D-1421-08 | g.chr10:21076186T>C | c.2813A>G | c.(2812-2814)tAc>tGc | p.Y938C |
| KIRC | 10 | 21124510 | 21124510 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CJ-6027-01A-11D-1669-08 | TCGA-CJ-6027-11A-01D-1669-08 | g.chr10:21124510C>A | c.1381G>T | c.(1381-1383)Gga>Tga | p.G461* |
| KIRC | 10 | 21158725 | 21158725 | + | Missense_Mutation | SNP | C | C | G | TCGA-B2-5635-01A-01D-1534-10 | TCGA-B2-5635-10A-01D-1535-10 | g.chr10:21158725C>G | c.526G>C | c.(526-528)Gaa>Caa | p.E176Q |
| KIRP | 10 | 21309109 | 21309109 | + | Silent | SNP | G | G | A | TCGA-B3-4104-01A-01D-1458-08 | TCGA-B3-4104-10A-01D-1458-08 | g.chr10:21309109G>A | c.186C>T | c.(184-186)ttC>ttT | p.F62F |
| LGG | 10 | 21074807 | 21074807 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A7TI-01A-11D-A33T-08 | TCGA-DU-A7TI-10A-01D-A33W-08 | g.chr10:21074807C>T | c.2914G>A | c.(2914-2916)Gag>Aag | p.E972K |
| LGG | 10 | 21074810 | 21074810 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:21074810C>A | c.2911G>T | c.(2911-2913)Gac>Tac | p.D971Y |
| LGG | 10 | 21097453 | 21097453 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-8168-01A-11D-2253-08 | TCGA-DU-8168-10A-01D-2253-08 | g.chr10:21097453G>A | c.2747C>T | c.(2746-2748)cCg>cTg | p.P916L |
| LGG | 10 | 21097515 | 21097515 | + | Silent | SNP | G | G | A | TCGA-E1-5304-01A-01D-1468-08 | TCGA-E1-5304-10A-01D-1468-08 | g.chr10:21097515G>A | c.2685C>T | c.(2683-2685)gaC>gaT | p.D895D |
| LGG | 10 | 21098829 | 21098829 | + | Splice_Site | SNP | T | T | C | TCGA-FG-A87N-01A-11D-A36O-08 | TCGA-FG-A87N-10A-01D-A367-08 | g.chr10:21098829T>C | | c.e25-2 | |
| LGG | 10 | 21101818 | 21101818 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:21101818C>T | c.2398G>A | c.(2398-2400)Gtc>Atc | p.V800I |
| LGG | 10 | 21120204 | 21120204 | + | Missense_Mutation | SNP | A | A | C | TCGA-E1-A7YK-01A-11D-A34A-08 | TCGA-E1-A7YK-10A-01D-A34A-08 | g.chr10:21120204A>C | c.1592T>G | c.(1591-1593)aTt>aGt | p.I531S |
| LGG | 10 | 21120450 | 21120450 | + | Missense_Mutation | SNP | G | G | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:21120450G>C | c.1512C>G | c.(1510-1512)gaC>gaG | p.D504E |
| LGG | 10 | 21139359 | 21139359 | + | Missense_Mutation | SNP | G | G | C | TCGA-DU-A7TA-01A-11D-A33T-08 | TCGA-DU-A7TA-10A-01D-A33W-08 | g.chr10:21139359G>C | c.1081C>G | c.(1081-1083)Caa>Gaa | p.Q361E |
| LGG | 10 | 21185916 | 21185916 | + | Missense_Mutation | SNP | C | C | A | TCGA-E1-A7YI-01A-11D-A34A-08 | TCGA-E1-A7YI-10A-01D-A34A-08 | g.chr10:21185916C>A | c.124G>T | c.(124-126)Gcc>Tcc | p.A42S |
| LGG | 10 | 21462709 | 21462709 | + | Silent | SNP | G | G | A | TCGA-VW-A8FI-01A-11D-A36O-08 | TCGA-VW-A8FI-10A-01D-A367-08 | g.chr10:21462709G>A | c.54C>T | c.(52-54)gtC>gtT | p.V18V |
| LIHC | 10 | 21104614 | 21104614 | + | Silent | SNP | G | G | T | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr10:21104614G>T | c.2181C>A | c.(2179-2181)acC>acA | p.T727T |
| LIHC | 10 | 21134239 | 21134239 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr10:21134239T>C | c.1175A>G | c.(1174-1176)gAc>gGc | p.D392G |
| LIHC | 10 | 21134258 | 21134258 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A39Z-01A-11D-A20W-10 | TCGA-DD-A39Z-11A-21D-A20W-10 | g.chr10:21134258T>C | c.1156A>G | c.(1156-1158)Agg>Ggg | p.R386G |
| LIHC | 10 | 21169807 | 21169807 | + | Silent | SNP | A | A | T | TCGA-DD-AACI-01A-11D-A40R-10 | TCGA-DD-AACI-10A-01D-A40U-10 | g.chr10:21169807A>T | c.396T>A | c.(394-396)gcT>gcA | p.A132A |
| LIHC | 10 | 21178773 | 21178773 | + | Splice_Site | SNP | C | C | A | TCGA-CC-A7IH-01A-11D-A33K-10 | TCGA-CC-A7IH-10A-01D-A33K-10 | g.chr10:21178773C>A | | c.e3+1 | |
| LIHC | 10 | 21178791 | 21178791 | + | Missense_Mutation | SNP | C | C | A | TCGA-2Y-A9GT-01A-11D-A382-10 | TCGA-2Y-A9GT-10A-01D-A385-10 | g.chr10:21178791C>A | c.241G>T | c.(241-243)Ggt>Tgt | p.G81C |
| LIHC | 10 | 21178796 | 21178796 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr10:21178796delT | c.236delA | c.(235-237)aatfs | p.N79fs |
| LUAD | 10 | 21074742 | 21074742 | + | Silent | SNP | G | G | A | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr10:21074742G>A | c.2979C>T | c.(2977-2979)taC>taT | p.Y993Y |
| LUAD | 10 | 21074756 | 21074756 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4397-01A-01D-1265-08 | TCGA-05-4397-10A-01D-1265-08 | g.chr10:21074756C>A | c.2965G>T | c.(2965-2967)Gat>Tat | p.D989Y |
| LUAD | 10 | 21074853 | 21074853 | + | Splice_Site | SNP | C | C | T | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chr10:21074853C>T | | c.e28-1 | |
| LUAD | 10 | 21101712 | 21101712 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr10:21101712G>A | c.2504C>T | c.(2503-2505)cCt>cTt | p.P835L |
| LUAD | 10 | 21101754 | 21101754 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z014-01A-01W-0746-08 | TCGA-17-Z014-11A-01W-0746-08 | g.chr10:21101754T>C | c.2462A>G | c.(2461-2463)tAt>tGt | p.Y821C |
| LUAD | 10 | 21101768 | 21101768 | + | Silent | SNP | G | G | A | TCGA-50-5072-01A-21D-1855-08 | TCGA-50-5072-10A-01D-1855-08 | g.chr10:21101768G>A | c.2448C>T | c.(2446-2448)gtC>gtT | p.V816V |
| LUAD | 10 | 21101791 | 21101791 | + | Missense_Mutation | SNP | C | C | G | TCGA-NJ-A4YI-01A-11D-A25L-08 | TCGA-NJ-A4YI-10A-01D-A25L-08 | g.chr10:21101791C>G | c.2425G>C | c.(2425-2427)Gtg>Ctg | p.V809L |
| LUAD | 10 | 21104601 | 21104606 | + | In_Frame_Del | DEL | TTACAC | TTACAC | - | TCGA-05-4244-01A-01D-1105-08 | TCGA-05-4244-10A-01D-1105-08 | g.chr10:21104601_21104606delTTACAC | c.2189_2194delGTGTAA | c.(2188-2196)agtgtaact>act | p.SV730del |
| LUAD | 10 | 21108395 | 21108395 | + | Silent | SNP | C | C | T | TCGA-55-6712-01A-11D-1855-08 | TCGA-55-6712-10A-01D-1855-08 | g.chr10:21108395C>T | c.2013G>A | c.(2011-2013)ccG>ccA | p.P671P |
| LUAD | 10 | 21108432 | 21108432 | + | Missense_Mutation | SNP | T | T | C | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr10:21108432T>C | c.1976A>G | c.(1975-1977)gAg>gGg | p.E659G |
| LUAD | 10 | 21115394 | 21115394 | + | Missense_Mutation | SNP | A | A | C | TCGA-78-7159-01A-11D-2036-08 | TCGA-78-7159-10A-01D-2036-08 | g.chr10:21115394A>C | c.1851T>G | c.(1849-1851)aaT>aaG | p.N617K |
| LUAD | 10 | 21115407 | 21115407 | + | Missense_Mutation | SNP | C | C | T | TCGA-73-7499-01A-11D-2184-08 | TCGA-73-7499-10A-01D-2184-08 | g.chr10:21115407C>T | c.1838G>A | c.(1837-1839)cGa>cAa | p.R613Q |
| LUAD | 10 | 21117556 | 21117556 | + | Missense_Mutation | SNP | T | T | C | TCGA-86-8585-01A-11D-2393-08 | TCGA-86-8585-10A-01D-2393-08 | g.chr10:21117556T>C | c.1679A>G | c.(1678-1680)tAt>tGt | p.Y560C |
| LUAD | 10 | 21120401 | 21120401 | + | Splice_Site | SNP | C | C | A | TCGA-17-Z014-01A-01W-0746-08 | TCGA-17-Z014-11A-01W-0746-08 | g.chr10:21120401C>A | | c.e15+1 | |
| LUAD | 10 | 21120446 | 21120446 | + | Missense_Mutation | SNP | G | G | C | TCGA-78-7149-01A-11D-2036-08 | TCGA-78-7149-10A-01D-2036-08 | g.chr10:21120446G>C | c.1516C>G | c.(1516-1518)Ctt>Gtt | p.L506V |
| LUAD | 10 | 21120447 | 21120447 | + | Silent | SNP | A | A | C | TCGA-67-4679-01B-01D-1753-08 | TCGA-67-4679-10A-01D-1753-08 | g.chr10:21120447A>C | c.1515T>G | c.(1513-1515)acT>acG | p.T505T |
| LUAD | 10 | 21124440 | 21124440 | + | Splice_Site | SNP | A | A | C | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr10:21124440A>C | | c.e14+1 | |
| LUAD | 10 | 21124531 | 21124531 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-99-8028-01A-11D-2238-08 | TCGA-99-8028-10A-01D-2238-08 | g.chr10:21124531C>A | c.1360G>T | c.(1360-1362)Gag>Tag | p.E454* |
| LUAD | 10 | 21134261 | 21134261 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-17-Z016-01A-01W-0746-08 | TCGA-17-Z016-11A-01W-0746-08 | g.chr10:21134261C>A | c.1153G>T | c.(1153-1155)Gga>Tga | p.G385* |
| LUAD | 10 | 21147170 | 21147170 | + | Splice_Site | SNP | C | C | A | TCGA-17-Z042-01A-01W-0746-08 | TCGA-17-Z042-11A-01W-0746-08 | g.chr10:21147170C>A | c.902G>T | c.(901-903)gGc>gTc | p.G301V |
| LUAD | 10 | 21147230 | 21147230 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chr10:21147230G>A | c.842C>T | c.(841-843)tCa>tTa | p.S281L |
| LUAD | 10 | 21148756 | 21148756 | + | Splice_Site | SNP | C | C | A | TCGA-86-8672-01A-21D-2393-08 | TCGA-86-8672-10A-01D-2393-08 | g.chr10:21148756C>A | | c.e8-1 | |
| LUAD | 10 | 21158739 | 21158739 | + | Missense_Mutation | SNP | T | T | A | TCGA-05-4390-01A-02D-1753-08 | TCGA-05-4390-10A-01D-1753-08 | g.chr10:21158739T>A | c.512A>T | c.(511-513)cAc>cTc | p.H171L |
| LUAD | 10 | 21169750 | 21169750 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-17-Z013-01A-01W-0746-08 | TCGA-17-Z013-11A-01W-0746-08 | g.chr10:21169750delG | c.453delC | c.(451-453)gccfs | p.A151fs |
| LUAD | 10 | 21186113 | 21186113 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr10:21186113C>A | c.22G>T | c.(22-24)Gat>Tat | p.D8Y |
| LUAD | 10 | 21250670 | 21250670 | + | Silent | SNP | C | C | T | TCGA-86-A456-01A-11D-A24D-08 | TCGA-86-A456-10A-01D-A24F-08 | g.chr10:21250670C>T | c.288G>A | c.(286-288)agG>agA | p.R96R |
| LUAD | 10 | 21250675 | 21250675 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr10:21250675C>A | c.283G>T | c.(283-285)Ggg>Tgg | p.G95W |
| LUAD | 10 | 21461315 | 21461315 | + | Missense_Mutation | SNP | T | T | A | TCGA-83-5908-01A-21D-2284-08 | TCGA-83-5908-10A-01D-2284-08 | g.chr10:21461315T>A | c.161A>T | c.(160-162)aAt>aTt | p.N54I |
| LUAD | 10 | 21461326 | 21461326 | + | Silent | SNP | C | C | T | TCGA-86-7701-01A-11D-2167-08 | TCGA-86-7701-10A-01D-2167-08 | g.chr10:21461326C>T | c.150G>A | c.(148-150)aaG>aaA | p.K50K |
| LUAD | 10 | 21461395 | 21461395 | + | Missense_Mutation | SNP | T | T | A | TCGA-69-7973-01A-11D-2184-08 | TCGA-69-7973-10A-01D-2184-08 | g.chr10:21461395T>A | c.81A>T | c.(79-81)aaA>aaT | p.K27N |
| LUSC | 10 | 21097437 | 21097437 | + | Splice_Site | SNP | A | A | G | TCGA-66-2763-01A-01D-1522-08 | TCGA-66-2763-11A-01D-1522-08 | g.chr10:21097437A>G | | c.e26+1 | |
| LUSC | 10 | 21108409 | 21108409 | + | Missense_Mutation | SNP | C | C | A | TCGA-46-3765-01A-01D-0983-08 | TCGA-46-3765-10A-01D-0983-08 | g.chr10:21108409C>A | c.1999G>T | c.(1999-2001)Gta>Tta | p.V667L |
| LUSC | 10 | 21112199 | 21112199 | + | Missense_Mutation | SNP | T | T | C | TCGA-22-4601-01A-01D-1441-08 | TCGA-22-4601-11A-01D-1441-08 | g.chr10:21112199T>C | c.1900A>G | c.(1900-1902)Aca>Gca | p.T634A |
| LUSC | 10 | 21115440 | 21115440 | + | Missense_Mutation | SNP | C | C | T | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr10:21115440C>T | c.1805G>A | c.(1804-1806)gGc>gAc | p.G602D |
| LUSC | 10 | 21120411 | 21120411 | + | Missense_Mutation | SNP | C | C | T | TCGA-34-5927-01A-11D-1817-08 | TCGA-34-5927-10A-01D-1817-08 | g.chr10:21120411C>T | c.1551G>A | c.(1549-1551)atG>atA | p.M517I |
| LUSC | 10 | 21134270 | 21134270 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2767-01A-01D-1522-08 | TCGA-66-2767-11A-01D-1522-08 | g.chr10:21134270C>G | c.1144G>C | c.(1144-1146)Gag>Cag | p.E382Q |
| LUSC | 10 | 21169795 | 21169795 | + | Silent | SNP | G | G | A | TCGA-22-5489-01A-01D-1632-08 | TCGA-22-5489-11A-01D-1632-08 | g.chr10:21169795G>A | c.408C>T | c.(406-408)ttC>ttT | p.F136F |
| LUSC | 10 | 21177072 | 21177072 | + | Missense_Mutation | SNP | G | G | A | TCGA-60-2721-01A-01D-1522-08 | TCGA-60-2721-11A-01D-1522-08 | g.chr10:21177072G>A | c.323C>T | c.(322-324)aCa>aTa | p.T108I |
| LUSC | 10 | 21185952 | 21185952 | + | Missense_Mutation | SNP | A | A | T | TCGA-39-5036-01A-01D-1441-08 | TCGA-39-5036-11A-01D-1441-08 | g.chr10:21185952A>T | c.88T>A | c.(88-90)Tat>Aat | p.Y30N |
| LUSC | 10 | 21250653 | 21250653 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2789-01A-01D-0983-08 | TCGA-66-2789-11A-01D-0983-08 | g.chr10:21250653G>C | c.305C>G | c.(304-306)aCg>aGg | p.T102R |
| OV | 10 | 21101810 | 21101810 | + | Silent | SNP | G | G | A | TCGA-24-1564-01A-01W-0551-08 | TCGA-24-1564-10A-01W-0551-08 | g.chr10:21101810G>A | c.2406C>T | c.(2404-2406)gaC>gaT | p.D802D |
| OV | 10 | 21134191 | 21134191 | + | Missense_Mutation | SNP | C | C | T | TCGA-25-2404-01A-01W-0799-08 | TCGA-25-2404-10A-01W-0799-08 | g.chr10:21134191C>T | c.1223G>A | c.(1222-1224)aGg>aAg | p.R408K |
| OV | 10 | 21185902 | 21185902 | + | Silent | SNP | C | C | T | TCGA-42-2588-01A-01D-1526-09 | TCGA-42-2588-10A-01D-1526-09 | g.chr10:21185902C>T | c.138G>A | c.(136-138)acG>acA | p.T46T |
| OV | 10 | 21461356 | 21461356 | + | Silent | SNP | G | G | A | TCGA-61-1915-01A-01W-0639-09 | TCGA-61-1915-11A-01W-0640-09 | g.chr10:21461356G>A | c.120C>T | c.(118-120)aaC>aaT | p.N40N |
| PAAD | 10 | 21074742 | 21074742 | + | Silent | SNP | G | G | A | TCGA-US-A77E-01A-11D-A32N-08 | TCGA-US-A77E-11A-11D-A32N-08 | g.chr10:21074742G>A | c.2979C>T | c.(2977-2979)taC>taT | p.Y993Y |
| PAAD | 10 | 21098813 | 21098813 | + | Missense_Mutation | SNP | G | G | A | TCGA-2J-AAB1-01A-11D-A40W-08 | TCGA-2J-AAB1-10A-01D-A40W-08 | g.chr10:21098813G>A | c.2533C>T | c.(2533-2535)Cgc>Tgc | p.R845C |
| PAAD | 10 | 21158753 | 21158753 | + | Silent | SNP | G | G | A | TCGA-2J-AABA-01A-21D-A40W-08 | TCGA-2J-AABA-10A-01D-A40W-08 | g.chr10:21158753G>A | c.498C>T | c.(496-498)gaC>gaT | p.D166D |
| PAAD | 10 | 21178809 | 21178809 | + | Missense_Mutation | SNP | T | T | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:21178809T>G | c.223A>C | c.(223-225)Aac>Cac | p.N75H |
| PAAD | 10 | 21309118 | 21309118 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:21309118C>T | c.177G>A | c.(175-177)aaG>aaA | p.K59K |
| PCPG | 10 | 21158716 | 21158716 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-SP-A6QG-01A-12D-A35I-08 | TCGA-SP-A6QG-10A-01D-A35G-08 | g.chr10:21158716G>A | c.535C>T | c.(535-537)Cga>Tga | p.R179* |
| PRAD | 10 | 21120417 | 21120417 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr10:21120417G>A | c.1545C>T | c.(1543-1545)tcC>tcT | p.S515S |
| PRAD | 10 | 21139370 | 21139370 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr10:21139370G>A | c.1070C>T | c.(1069-1071)aCa>aTa | p.T357I |
| PRAD | 10 | 21158736 | 21158736 | + | Missense_Mutation | SNP | G | G | A | TCGA-HC-A6AN-01A-11D-A30E-08 | TCGA-HC-A6AN-10A-01D-A30H-08 | g.chr10:21158736G>A | c.515C>T | c.(514-516)aCg>aTg | p.T172M |
| PRAD | 10 | 21169734 | 21169734 | + | Missense_Mutation | SNP | G | G | A | TCGA-V1-A8WV-01A-11D-A377-08 | TCGA-V1-A8WV-10A-01D-A37A-08 | g.chr10:21169734G>A | c.469C>T | c.(469-471)Cac>Tac | p.H157Y |
| PRAD | 10 | 21250654 | 21250654 | + | Missense_Mutation | SNP | T | T | C | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr10:21250654T>C | c.304A>G | c.(304-306)Acg>Gcg | p.T102A |
| READ | 10 | 21074816 | 21074816 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr10:21074816C>T | c.2905G>A | c.(2905-2907)Gat>Aat | p.D969N |
| READ | 10 | 21098789 | 21098789 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:21098789C>T | c.2557G>A | c.(2557-2559)Gac>Aac | p.D853N |
| READ | 10 | 21124510 | 21124510 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr10:21124510C>A | c.1381G>T | c.(1381-1383)Gga>Tga | p.G461* |
| READ | 10 | 21139426 | 21139426 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:21139426T>G | c.1014A>C | c.(1012-1014)aaA>aaC | p.K338N |
| READ | 10 | 21177028 | 21177028 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:21177028C>A | c.367G>T | c.(367-369)Gag>Tag | p.E123* |
| SARC | 10 | 21129758 | 21129758 | + | Silent | SNP | C | C | T | TCGA-X6-A7WD-01A-21D-A351-09 | TCGA-X6-A7WD-10A-01D-A351-09 | g.chr10:21129758C>T | c.1248G>A | c.(1246-1248)ttG>ttA | p.L416L |
| SKCM | 10 | 21074700 | 21074700 | + | Silent | SNP | C | C | T | TCGA-EE-A29V-06A-12D-A197-08 | TCGA-EE-A29V-10A-01D-A199-08 | g.chr10:21074700C>T | c.3021G>A | c.(3019-3021)gcG>gcA | p.A1007A |
| SKCM | 10 | 21074722 | 21074722 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1Q6-06A-11D-A196-08 | TCGA-D3-A1Q6-10A-01D-A198-08 | g.chr10:21074722C>T | c.2999G>A | c.(2998-3000)gGg>gAg | p.G1000E |
| SKCM | 10 | 21074740 | 21074740 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JD-06A-11D-A19A-08 | TCGA-D3-A2JD-10A-01D-A19A-08 | g.chr10:21074740C>T | c.2981G>A | c.(2980-2982)gGc>gAc | p.G994D |
| SKCM | 10 | 21074778 | 21074778 | + | Silent | SNP | G | G | A | TCGA-EE-A3JE-06A-11D-A20D-08 | TCGA-EE-A3JE-10A-01D-A20D-08 | g.chr10:21074778G>A | c.2943C>T | c.(2941-2943)atC>atT | p.I981I |
| SKCM | 10 | 21074807 | 21074807 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21074807C>T | c.2914G>A | c.(2914-2916)Gag>Aag | p.E972K |
| SKCM | 10 | 21074810 | 21074810 | + | Missense_Mutation | SNP | C | C | T | TCGA-RP-A694-06A-11D-A30X-08 | TCGA-RP-A694-10A-01D-A30X-08 | g.chr10:21074810C>T | c.2911G>A | c.(2911-2913)Gac>Aac | p.D971N |
| SKCM | 10 | 21074831 | 21074831 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A195-06A-11D-A196-08 | TCGA-ER-A195-10A-01D-A198-08 | g.chr10:21074831C>T | c.2890G>A | c.(2890-2892)Gat>Aat | p.D964N |
| SKCM | 10 | 21076194 | 21076194 | + | Silent | SNP | G | G | A | TCGA-EE-A2MP-06A-11D-A197-08 | TCGA-EE-A2MP-10A-01D-A199-08 | g.chr10:21076194G>A | c.2805C>T | c.(2803-2805)ggC>ggT | p.G935G |
| SKCM | 10 | 21097533 | 21097533 | + | Silent | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr10:21097533G>A | c.2667C>T | c.(2665-2667)ttC>ttT | p.F889F |
| SKCM | 10 | 21097533 | 21097533 | + | Silent | SNP | G | G | A | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr10:21097533G>A | c.2667C>T | c.(2665-2667)ttC>ttT | p.F889F |
| SKCM | 10 | 21097555 | 21097555 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:21097555C>T | c.2645G>A | c.(2644-2646)cGa>cAa | p.R882Q |
| SKCM | 10 | 21097567 | 21097567 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19D-06A-11D-A197-08 | TCGA-ER-A19D-10A-01D-A199-08 | g.chr10:21097567C>T | c.2633G>A | c.(2632-2634)cGa>cAa | p.R878Q |
| SKCM | 10 | 21098760 | 21098760 | + | Silent | SNP | C | C | T | TCGA-D3-A3C8-06A-12D-A19A-08 | TCGA-D3-A3C8-10A-01D-A19A-08 | g.chr10:21098760C>T | c.2586G>A | c.(2584-2586)caG>caA | p.Q862Q |
| SKCM | 10 | 21098779 | 21098779 | + | Missense_Mutation | SNP | G | G | A | TCGA-RP-A695-06A-11D-A30X-08 | TCGA-RP-A695-10A-01D-A30X-08 | g.chr10:21098779G>A | c.2567C>T | c.(2566-2568)cCc>cTc | p.P856L |
| SKCM | 10 | 21098807 | 21098807 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr10:21098807C>T | c.2539G>A | c.(2539-2541)Gat>Aat | p.D847N |
| SKCM | 10 | 21101729 | 21101729 | + | Silent | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:21101729C>T | c.2487G>A | c.(2485-2487)gtG>gtA | p.V829V |
| SKCM | 10 | 21101732 | 21101732 | + | Silent | SNP | G | G | A | TCGA-D3-A2JF-06A-11D-A196-08 | TCGA-D3-A2JF-10A-01D-A198-08 | g.chr10:21101732G>A | c.2484C>T | c.(2482-2484)atC>atT | p.I828I |
| SKCM | 10 | 21101732 | 21101732 | + | Silent | SNP | G | G | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr10:21101732G>A | c.2484C>T | c.(2482-2484)atC>atT | p.I828I |
| SKCM | 10 | 21101786 | 21101786 | + | Silent | SNP | C | C | T | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr10:21101786C>T | c.2430G>A | c.(2428-2430)agG>agA | p.R810R |
| SKCM | 10 | 21101806 | 21101806 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr10:21101806G>A | c.2410C>T | c.(2410-2412)Cct>Tct | p.P804S |
| SKCM | 10 | 21101818 | 21101818 | + | Missense_Mutation | SNP | C | C | T | TCGA-EB-A5KH-06A-11D-A27K-08 | TCGA-EB-A5KH-10A-01D-A27N-08 | g.chr10:21101818C>T | c.2398G>A | c.(2398-2400)Gtc>Atc | p.V800I |
| SKCM | 10 | 21101828 | 21101828 | + | Silent | SNP | G | G | A | TCGA-EE-A2MM-06A-11D-A196-08 | TCGA-EE-A2MM-10A-01D-A198-08 | g.chr10:21101828G>A | c.2388C>T | c.(2386-2388)ggC>ggT | p.G796G |
| SKCM | 10 | 21101837 | 21101837 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr10:21101837C>T | c.2379G>A | c.(2377-2379)aaG>aaA | p.K793K |
| SKCM | 10 | 21102879 | 21102879 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr10:21102879G>A | c.2335C>T | c.(2335-2337)Cat>Tat | p.H779Y |
| SKCM | 10 | 21102879 | 21102879 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr10:21102879G>A | c.2335C>T | c.(2335-2337)Cat>Tat | p.H779Y |
| SKCM | 10 | 21102932 | 21102932 | + | Missense_Mutation | SNP | G | G | T | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr10:21102932G>T | c.2282C>A | c.(2281-2283)cCa>cAa | p.P761Q |
| SKCM | 10 | 21102957 | 21102957 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21102957C>T | c.2257G>A | c.(2257-2259)Gac>Aac | p.D753N |
| SKCM | 10 | 21104619 | 21104619 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr10:21104619C>T | c.2176G>A | c.(2176-2178)Gct>Act | p.A726T |
| SKCM | 10 | 21106570 | 21106570 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr10:21106570C>T | c.2107G>A | c.(2107-2109)Gag>Aag | p.E703K |
| SKCM | 10 | 21106608 | 21106608 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr10:21106608C>T | c.2069G>A | c.(2068-2070)gGa>gAa | p.G690E |
| SKCM | 10 | 21108351 | 21108351 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr10:21108351G>A | | c.e20+1 | |
| SKCM | 10 | 21108367 | 21108367 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21108367C>T | c.2041G>A | c.(2041-2043)Gag>Aag | p.E681K |
| SKCM | 10 | 21108375 | 21108375 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1Q6-06A-11D-A196-08 | TCGA-D3-A1Q6-10A-01D-A198-08 | g.chr10:21108375C>T | c.2033G>A | c.(2032-2034)cGa>cAa | p.R678Q |
| SKCM | 10 | 21108375 | 21108375 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr10:21108375C>T | c.2033G>A | c.(2032-2034)cGa>cAa | p.R678Q |
| SKCM | 10 | 21108397 | 21108397 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr10:21108397G>A | c.2011C>T | c.(2011-2013)Ccg>Tcg | p.P671S |
| SKCM | 10 | 21108411 | 21108411 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr10:21108411G>A | c.1997C>T | c.(1996-1998)cCg>cTg | p.P666L |
| SKCM | 10 | 21112212 | 21112212 | + | Silent | SNP | C | C | T | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr10:21112212C>T | c.1887G>A | c.(1885-1887)gaG>gaA | p.E629E |
| SKCM | 10 | 21115400 | 21115400 | + | Silent | SNP | C | C | T | TCGA-EB-A5UN-06A-11D-A30X-08 | TCGA-EB-A5UN-10A-01D-A30X-08 | g.chr10:21115400C>T | c.1845G>A | c.(1843-1845)aaG>aaA | p.K615K |
| SKCM | 10 | 21115400 | 21115400 | + | Silent | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr10:21115400C>T | c.1845G>A | c.(1843-1845)aaG>aaA | p.K615K |
| SKCM | 10 | 21115411 | 21115411 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3MU-06A-11D-A21A-08 | TCGA-D3-A3MU-10A-01D-A21A-08 | g.chr10:21115411C>T | c.1834G>A | c.(1834-1836)Gaa>Aaa | p.E612K |
| SKCM | 10 | 21115453 | 21115453 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr10:21115453C>T | c.1792G>A | c.(1792-1794)Gaa>Aaa | p.E598K |
| SKCM | 10 | 21120139 | 21120139 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GM-06B-11D-A196-08 | TCGA-EE-A2GM-10A-01D-A198-08 | g.chr10:21120139C>T | c.1657G>A | c.(1657-1659)Gaa>Aaa | p.E553K |
| SKCM | 10 | 21120147 | 21120147 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21120147C>T | c.1649G>A | c.(1648-1650)aGg>aAg | p.R550K |
| SKCM | 10 | 21120160 | 21120160 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51J-06A-11D-A25O-08 | TCGA-D3-A51J-10A-01D-A25O-08 | g.chr10:21120160G>A | c.1636C>T | c.(1636-1638)Ctt>Ttt | p.L546F |
| SKCM | 10 | 21120162 | 21120162 | + | Missense_Mutation | SNP | A | A | C | TCGA-D9-A1JW-06A-11D-A19A-08 | TCGA-D9-A1JW-10A-01D-A19A-08 | g.chr10:21120162A>C | c.1634T>G | c.(1633-1635)aTc>aGc | p.I545S |
| SKCM | 10 | 21120176 | 21120176 | + | Missense_Mutation | SNP | C | C | T | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr10:21120176C>T | c.1620G>A | c.(1618-1620)atG>atA | p.M540I |
| SKCM | 10 | 21120193 | 21120193 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21120193C>T | c.1603G>A | c.(1603-1605)Gga>Aga | p.G535R |
| SKCM | 10 | 21120197 | 21120197 | + | Silent | SNP | C | C | T | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr10:21120197C>T | c.1599G>A | c.(1597-1599)ggG>ggA | p.G533G |
| SKCM | 10 | 21120197 | 21120197 | + | Silent | SNP | C | C | T | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr10:21120197C>T | c.1599G>A | c.(1597-1599)ggG>ggA | p.G533G |
| SKCM | 10 | 21120416 | 21120416 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JF-06A-11D-A196-08 | TCGA-D3-A2JF-10A-01D-A198-08 | g.chr10:21120416C>T | c.1546G>A | c.(1546-1548)Gag>Aag | p.E516K |
| SKCM | 10 | 21120418 | 21120418 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A5GN-06A-11D-A27K-08 | TCGA-D3-A5GN-10A-01D-A27N-08 | g.chr10:21120418G>A | c.1544C>T | c.(1543-1545)tCc>tTc | p.S515F |
| SKCM | 10 | 21120485 | 21120485 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19D-06A-11D-A197-08 | TCGA-ER-A19D-10A-01D-A199-08 | g.chr10:21120485C>T | c.1477G>A | c.(1477-1479)Gaa>Aaa | p.E493K |
| SKCM | 10 | 21120489 | 21120489 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21120489C>T | c.1473G>A | c.(1471-1473)gaG>gaA | p.E491E |
| SKCM | 10 | 21124456 | 21124456 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr10:21124456C>A | c.1435G>T | c.(1435-1437)Gag>Tag | p.E479* |
| SKCM | 10 | 21124509 | 21124509 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr10:21124509C>T | c.1382G>A | c.(1381-1383)gGa>gAa | p.G461E |
| SKCM | 10 | 21124516 | 21124516 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A265-06A-21D-A197-08 | TCGA-GN-A265-10A-01D-A199-08 | g.chr10:21124516C>T | c.1375G>A | c.(1375-1377)Ggg>Agg | p.G459R |
| SKCM | 10 | 21129735 | 21129735 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr10:21129735C>T | c.1271G>A | c.(1270-1272)gGa>gAa | p.G424E |
| SKCM | 10 | 21129740 | 21129740 | + | Silent | SNP | C | C | T | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr10:21129740C>T | c.1266G>A | c.(1264-1266)ggG>ggA | p.G422G |
| SKCM | 10 | 21129757 | 21129757 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr10:21129757C>T | c.1249G>A | c.(1249-1251)Gaa>Aaa | p.E417K |
| SKCM | 10 | 21129779 | 21129779 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chr10:21129779C>T | | c.e13-1 | |
| SKCM | 10 | 21134200 | 21134200 | + | Missense_Mutation | SNP | T | T | C | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr10:21134200T>C | c.1214A>G | c.(1213-1215)aAc>aGc | p.N405S |
| SKCM | 10 | 21134298 | 21134298 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A2MT-06A-11D-A197-08 | TCGA-EE-A2MT-10A-01D-A199-08 | g.chr10:21134298C>T | | c.e12-1 | |
| SKCM | 10 | 21139336 | 21139336 | + | Silent | SNP | C | C | T | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr10:21139336C>T | c.1104G>A | c.(1102-1104)aaG>aaA | p.K368K |
| SKCM | 10 | 21141544 | 21141544 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr10:21141544C>T | c.938G>A | c.(937-939)gGa>gAa | p.G313E |
| SKCM | 10 | 21141544 | 21141544 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19E-06A-11D-A197-08 | TCGA-ER-A19E-10A-01D-A199-08 | g.chr10:21141544C>T | c.938G>A | c.(937-939)gGa>gAa | p.G313E |
| SKCM | 10 | 21141545 | 21141545 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JP-06A-11D-A19A-08 | TCGA-D3-A2JP-10A-01D-A19A-08 | g.chr10:21141545C>T | c.937G>A | c.(937-939)Gga>Aga | p.G313R |
| SKCM | 10 | 21141554 | 21141554 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chr10:21141554C>T | c.928G>A | c.(928-930)Gaa>Aaa | p.E310K |
| SKCM | 10 | 21148696 | 21148696 | + | Silent | SNP | A | A | C | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr10:21148696A>C | c.744T>G | c.(742-744)ccT>ccG | p.P248P |
| SKCM | 10 | 21148719 | 21148719 | + | Missense_Mutation | SNP | C | C | T | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr10:21148719C>T | c.721G>A | c.(721-723)Gat>Aat | p.D241N |
| SKCM | 10 | 21148728 | 21148728 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr10:21148728C>T | c.712G>A | c.(712-714)Gaa>Aaa | p.E238K |
| SKCM | 10 | 21157616 | 21157616 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21157616C>T | c.661G>A | c.(661-663)Gaa>Aaa | p.E221K |
| SKCM | 10 | 21158759 | 21158759 | + | Silent | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr10:21158759C>T | c.492G>A | c.(490-492)agG>agA | p.R164R |
| SKCM | 10 | 21158759 | 21158759 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21158759C>T | c.492G>A | c.(490-492)agG>agA | p.R164R |
| SKCM | 10 | 21169763 | 21169763 | + | Missense_Mutation | SNP | T | T | G | TCGA-EE-A3AD-06A-11D-A196-08 | TCGA-EE-A3AD-10A-01D-A198-08 | g.chr10:21169763T>G | c.440A>C | c.(439-441)gAg>gCg | p.E147A |
| SKCM | 10 | 21169768 | 21169768 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZA-06A-11D-A197-08 | TCGA-FS-A1ZA-10A-01D-A199-08 | g.chr10:21169768G>A | c.435C>T | c.(433-435)ccC>ccT | p.P145P |
| SKCM | 10 | 21169773 | 21169773 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr10:21169773C>T | c.430G>A | c.(430-432)Gag>Aag | p.E144K |
| SKCM | 10 | 21169800 | 21169800 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chr10:21169800C>T | c.403G>A | c.(403-405)Gga>Aga | p.G135R |
| SKCM | 10 | 21178778 | 21178778 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21178778G>A | c.254C>T | c.(253-255)tCt>tTt | p.S85F |
| SKCM | 10 | 21178791 | 21178791 | + | Missense_Mutation | SNP | C | C | T | TCGA-OD-A75X-06A-12D-A32N-08 | TCGA-OD-A75X-10A-01D-A32N-08 | g.chr10:21178791C>T | c.241G>A | c.(241-243)Ggt>Agt | p.G81S |
| SKCM | 10 | 21178808 | 21178808 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr10:21178808T>A | c.224A>T | c.(223-225)aAc>aTc | p.N75I |
| SKCM | 10 | 21178817 | 21178817 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr10:21178817G>A | c.215C>T | c.(214-216)cCt>cTt | p.P72L |
| SKCM | 10 | 21185889 | 21185889 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A17X-06A-11D-A197-08 | TCGA-EE-A17X-10A-01D-A199-08 | g.chr10:21185889C>T | c.151G>A | c.(151-153)Gat>Aat | p.D51N |
| SKCM | 10 | 21185901 | 21185901 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr10:21185901C>T | c.139G>A | c.(139-141)Gaa>Aaa | p.E47K |
| SKCM | 10 | 21185923 | 21185923 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZS-06A-12D-A197-08 | TCGA-FS-A1ZS-10A-01D-A199-08 | g.chr10:21185923C>T | c.117G>A | c.(115-117)atG>atA | p.M39I |
| SKCM | 10 | 21185941 | 21185941 | + | Silent | SNP | A | A | C | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:21185941A>C | c.99T>G | c.(97-99)gtT>gtG | p.V33V |
| SKCM | 10 | 21186092 | 21186092 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21186092C>T | c.43G>A | c.(43-45)Gaa>Aaa | p.E15K |
| SKCM | 10 | 21250658 | 21250658 | + | Silent | SNP | G | G | A | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr10:21250658G>A | c.300C>T | c.(298-300)atC>atT | p.I100I |
| SKCM | 10 | 21250658 | 21250658 | + | Silent | SNP | G | G | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr10:21250658G>A | c.300C>T | c.(298-300)atC>atT | p.I100I |
| SKCM | 10 | 21250667 | 21250667 | + | Silent | SNP | G | G | A | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr10:21250667G>A | c.291C>T | c.(289-291)ggC>ggT | p.G97G |
| SKCM | 10 | 21309073 | 21309073 | + | Silent | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr10:21309073C>T | c.222G>A | c.(220-222)ctG>ctA | p.L74L |
| SKCM | 10 | 21309078 | 21309078 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr10:21309078G>A | c.217C>T | c.(217-219)Cgc>Tgc | p.R73C |
| SKCM | 10 | 21309123 | 21309123 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:21309123G>A | c.172C>T | c.(172-174)Ccg>Tcg | p.P58S |