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 | 15 | 67893072 | 67893072 | + | Missense_Mutation | SNP | G | G | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr15:67893072G>T | c.530G>T | c.(529-531)gGa>gTa | p.G177V |
BLCA | 15 | 67923241 | 67923241 | + | Silent | SNP | G | G | A | TCGA-XF-AAN2-01A-11D-A42E-08 | TCGA-XF-AAN2-10A-01D-A42H-08 | g.chr15:67923241G>A | c.561G>A | c.(559-561)ccG>ccA | p.P187P |
BLCA | 15 | 67938757 | 67938757 | + | Missense_Mutation | SNP | G | G | T | TCGA-ZF-A9RD-01A-11D-A42E-08 | TCGA-ZF-A9RD-10A-01D-A42H-08 | g.chr15:67938757G>T | c.686G>T | c.(685-687)gGa>gTa | p.G229V |
BLCA | 15 | 67950939 | 67950939 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chr15:67950939G>A | c.785G>A | c.(784-786)aGa>aAa | p.R262K |
BLCA | 15 | 68040934 | 68040934 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A6TA-01A-12D-A339-08 | TCGA-FD-A6TA-10A-21D-A339-08 | g.chr15:68040934G>A | c.1129G>A | c.(1129-1131)Gat>Aat | p.D377N |
BRCA | 15 | 67873162 | 67873162 | + | Splice_Site | SNP | G | G | C | TCGA-A2-A0YI-01A-31D-A10M-09 | TCGA-A2-A0YI-10A-01D-A10M-09 | g.chr15:67873162G>C | | c.e4+1 | |
BRCA | 15 | 68061993 | 68061993 | + | Silent | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr15:68061993C>T | c.1188C>T | c.(1186-1188)atC>atT | p.I396I |
COAD | 15 | 67835755 | 67835755 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:67835755G>A | c.82G>A | c.(82-84)Gcg>Acg | p.A28T |
COAD | 15 | 67855642 | 67855642 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr15:67855642G>A | c.206G>A | c.(205-207)cGa>cAa | p.R69Q |
COAD | 15 | 67873159 | 67873159 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-6782-01A-11D-1835-10 | TCGA-A6-6782-10A-01D-1835-10 | g.chr15:67873159G>T | c.320G>T | c.(319-321)aGa>aTa | p.R107I |
COAD | 15 | 67893022 | 67893022 | + | Splice_Site | SNP | G | G | T | TCGA-G4-6321-01A-11D-1719-10 | TCGA-G4-6321-10A-01D-1720-10 | g.chr15:67893022G>T | | c.e8-1 | |
COADREAD | 15 | 67835755 | 67835755 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:67835755G>A | c.82G>A | c.(82-84)Gcg>Acg | p.A28T |
COADREAD | 15 | 67855642 | 67855642 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr15:67855642G>A | c.206G>A | c.(205-207)cGa>cAa | p.R69Q |
COADREAD | 15 | 67873159 | 67873159 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-6782-01A-11D-1835-10 | TCGA-A6-6782-10A-01D-1835-10 | g.chr15:67873159G>T | c.320G>T | c.(319-321)aGa>aTa | p.R107I |
COADREAD | 15 | 67893022 | 67893022 | + | Splice_Site | SNP | G | G | T | TCGA-G4-6321-01A-11D-1719-10 | TCGA-G4-6321-10A-01D-1720-10 | g.chr15:67893022G>T | | c.e8-1 | |
COADREAD | 15 | 67985905 | 67985905 | + | Splice_Site | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:67985905C>T | c.971C>T | c.(970-972)gCg>gTg | p.A324V |
COADREAD | 15 | 67995740 | 67995740 | + | Missense_Mutation | SNP | T | T | A | TCGA-AG-3593-01A-01W-0831-10 | TCGA-AG-3593-10A-01W-0831-10 | g.chr15:67995740T>A | c.1038T>A | c.(1036-1038)ttT>ttA | p.F346L |
ESCA | 15 | 67878257 | 67878257 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A8NV-01A-11D-A37C-09 | TCGA-L5-A8NV-11A-11D-A37F-09 | g.chr15:67878257C>T | c.352C>T | c.(352-354)Cat>Tat | p.H118Y |
ESCA | 15 | 67923233 | 67923233 | + | Missense_Mutation | SNP | C | C | G | TCGA-LN-A49R-01A-11D-A247-09 | TCGA-LN-A49R-10A-01D-A247-09 | g.chr15:67923233C>G | c.553C>G | c.(553-555)Cat>Gat | p.H185D |
ESCA | 15 | 68061972 | 68061972 | + | Silent | SNP | G | G | A | TCGA-2H-A9GL-01A-12D-A37C-09 | TCGA-2H-A9GL-11A-11D-A37F-09 | g.chr15:68061972G>A | c.1167G>A | c.(1165-1167)tcG>tcA | p.S389S |
GBMLGG | 15 | 67878228 | 67878228 | + | Splice_Site | SNP | C | C | T | TCGA-DH-A66B-01A-11D-A29Q-08 | TCGA-DH-A66B-10A-01D-A29Q-08 | g.chr15:67878228C>T | c.323C>T | c.(322-324)gCc>gTc | p.A108V |
GBMLGG | 15 | 67985893 | 67985893 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:67985893A>C | c.959A>C | c.(958-960)aAt>aCt | p.N320T |
HNSC | 15 | 67873100 | 67873100 | + | Silent | SNP | C | C | T | TCGA-CN-5360-01A-01D-1434-08 | TCGA-CN-5360-10A-01D-1434-08 | g.chr15:67873100C>T | c.261C>T | c.(259-261)tcC>tcT | p.S87S |
HNSC | 15 | 67873104 | 67873104 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-6995-01A-31D-2012-08 | TCGA-CN-6995-10A-01D-2013-08 | g.chr15:67873104G>T | c.265G>T | c.(265-267)Gta>Tta | p.V89L |
HNSC | 15 | 67995696 | 67995696 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-6934-01A-11D-1912-08 | TCGA-CV-6934-10A-01D-1912-08 | g.chr15:67995696C>A | c.994C>A | c.(994-996)Cag>Aag | p.Q332K |
HNSC | 15 | 68040920 | 68040920 | + | Missense_Mutation | SNP | T | T | A | TCGA-QK-A64Z-01A-11D-A30E-08 | TCGA-QK-A64Z-10A-01D-A30H-08 | g.chr15:68040920T>A | c.1115T>A | c.(1114-1116)cTg>cAg | p.L372Q |
KIPAN | 15 | 67956981 | 67956981 | + | Missense_Mutation | SNP | G | G | C | TCGA-BQ-5878-01A-11D-1589-08 | TCGA-BQ-5878-11A-01D-1589-08 | g.chr15:67956981G>C | c.845G>C | c.(844-846)aGa>aCa | p.R282T |
KIPAN | 15 | 67985904 | 67985904 | + | Missense_Mutation | SNP | G | G | T | TCGA-DW-7840-01A-11D-2136-08 | TCGA-DW-7840-10A-01D-2136-08 | g.chr15:67985904G>T | c.970G>T | c.(970-972)Gcg>Tcg | p.A324S |
KIPAN | 15 | 68099075 | 68099075 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-4804-01A-02D-1373-10 | TCGA-BP-4804-11A-01D-1373-10 | g.chr15:68099075A>G | c.1334A>G | c.(1333-1335)cAg>cGg | p.Q445R |
KIRC | 15 | 68099075 | 68099075 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-4804-01A-02D-1373-10 | TCGA-BP-4804-11A-01D-1373-10 | g.chr15:68099075A>G | c.1334A>G | c.(1333-1335)cAg>cGg | p.Q445R |
KIRP | 15 | 67956981 | 67956981 | + | Missense_Mutation | SNP | G | G | C | TCGA-BQ-5878-01A-11D-1589-08 | TCGA-BQ-5878-11A-01D-1589-08 | g.chr15:67956981G>C | c.845G>C | c.(844-846)aGa>aCa | p.R282T |
KIRP | 15 | 67985904 | 67985904 | + | Missense_Mutation | SNP | G | G | T | TCGA-DW-7840-01A-11D-2136-08 | TCGA-DW-7840-10A-01D-2136-08 | g.chr15:67985904G>T | c.970G>T | c.(970-972)Gcg>Tcg | p.A324S |
LGG | 15 | 67878228 | 67878228 | + | Splice_Site | SNP | C | C | T | TCGA-DH-A66B-01A-11D-A29Q-08 | TCGA-DH-A66B-10A-01D-A29Q-08 | g.chr15:67878228C>T | c.323C>T | c.(322-324)gCc>gTc | p.A108V |
LGG | 15 | 67985893 | 67985893 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:67985893A>C | c.959A>C | c.(958-960)aAt>aCt | p.N320T |
LIHC | 15 | 67835762 | 67835762 | + | Missense_Mutation | SNP | A | A | G | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr15:67835762A>G | c.89A>G | c.(88-90)gAc>gGc | p.D30G |
LUAD | 15 | 67878233 | 67878233 | + | Missense_Mutation | SNP | A | A | C | TCGA-55-6968-01A-11D-1945-08 | TCGA-55-6968-11A-01D-1945-08 | g.chr15:67878233A>C | c.328A>C | c.(328-330)Aag>Cag | p.K110Q |
LUAD | 15 | 67878235 | 67878235 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-6968-01A-11D-1945-08 | TCGA-55-6968-11A-01D-1945-08 | g.chr15:67878235G>C | c.330G>C | c.(328-330)aaG>aaC | p.K110N |
LUAD | 15 | 67879196 | 67879196 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-6985-01A-11D-1945-08 | TCGA-55-6985-11A-01D-1945-08 | g.chr15:67879196G>T | c.376G>T | c.(376-378)Gcc>Tcc | p.A126S |
LUAD | 15 | 67885300 | 67885300 | + | Silent | SNP | A | A | T | TCGA-69-8255-01A-11D-2284-08 | TCGA-69-8255-10A-01D-2284-08 | g.chr15:67885300A>T | c.468A>T | c.(466-468)ctA>ctT | p.L156L |
LUAD | 15 | 67893060 | 67893060 | + | Missense_Mutation | SNP | G | G | C | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr15:67893060G>C | c.518G>C | c.(517-519)gGt>gCt | p.G173A |
LUAD | 15 | 68065081 | 68065081 | + | Silent | SNP | A | A | G | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr15:68065081A>G | c.1233A>G | c.(1231-1233)gaA>gaG | p.E411E |
LUSC | 15 | 67950889 | 67950889 | + | Splice_Site | SNP | A | A | T | TCGA-63-5128-01A-01D-1441-08 | TCGA-63-5128-10A-01D-1441-08 | g.chr15:67950889A>T | | c.e12-1 | |
READ | 15 | 67985905 | 67985905 | + | Splice_Site | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:67985905C>T | c.971C>T | c.(970-972)gCg>gTg | p.A324V |
READ | 15 | 67995740 | 67995740 | + | Missense_Mutation | SNP | T | T | A | TCGA-AG-3593-01A-01W-0831-10 | TCGA-AG-3593-10A-01W-0831-10 | g.chr15:67995740T>A | c.1038T>A | c.(1036-1038)ttT>ttA | p.F346L |
SARC | 15 | 67950923 | 67950923 | + | Missense_Mutation | SNP | G | G | C | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr15:67950923G>C | c.769G>C | c.(769-771)Gaa>Caa | p.E257Q |
SKCM | 15 | 67878236 | 67878236 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr15:67878236C>T | c.331C>T | c.(331-333)Cct>Tct | p.P111S |
SKCM | 15 | 67923225 | 67923225 | + | Splice_Site | SNP | G | G | A | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr15:67923225G>A | | c.e9-1 | |
SKCM | 15 | 67985858 | 67985858 | + | Silent | SNP | G | G | T | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr15:67985858G>T | c.924G>T | c.(922-924)ctG>ctT | p.L308L |
SKCM | 15 | 67995676 | 67995676 | + | Splice_Site | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:67995676C>T | c.974C>T | c.(973-975)cCt>cTt | p.P325L |
SKCM | 15 | 68020265 | 68020265 | + | Silent | SNP | G | G | A | TCGA-D3-A51J-06A-11D-A25O-08 | TCGA-D3-A51J-10A-01D-A25O-08 | g.chr15:68020265G>A | c.1056G>A | c.(1054-1056)ggG>ggA | p.G352G |
SKCM | 15 | 68040913 | 68040913 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr15:68040913C>T | c.1108C>T | c.(1108-1110)Cag>Tag | p.Q370* |
SKCM | 15 | 68061944 | 68061944 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19W-06A-41D-A23B-08 | TCGA-ER-A19W-10A-01D-A23B-08 | g.chr15:68061944C>T | c.1139C>T | c.(1138-1140)tCg>tTg | p.S380L |