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 | 3 | 36570404 | 36570406 | + | In_Frame_Del | DEL | AGA | AGA | - | TCGA-OR-A5LB-01A-11D-A29I-10 | TCGA-OR-A5LB-10A-01D-A29L-10 | g.chr3:36570404_36570406delAGA | c.1037_1039delAGA | c.(1036-1041)gagaag>gag | p.K347del |
BLCA | 3 | 36422160 | 36422160 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr3:36422160G>A | c.25G>A | c.(25-27)Gag>Aag | p.E9K |
BLCA | 3 | 36524568 | 36524568 | + | Missense_Mutation | SNP | G | G | A | TCGA-GD-A3OP-01A-21D-A21Z-08 | TCGA-GD-A3OP-10A-01D-A21Z-08 | g.chr3:36524568G>A | c.473G>A | c.(472-474)cGg>cAg | p.R158Q |
BLCA | 3 | 36527655 | 36527655 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-AAN2-01A-11D-A42E-08 | TCGA-XF-AAN2-10A-01D-A42H-08 | g.chr3:36527655G>A | c.601G>A | c.(601-603)Gag>Aag | p.E201K |
BLCA | 3 | 36527675 | 36527675 | + | Silent | SNP | C | C | T | TCGA-XF-A9ST-01A-11D-A42E-08 | TCGA-XF-A9ST-10A-01D-A42H-08 | g.chr3:36527675C>T | c.621C>T | c.(619-621)acC>acT | p.T207T |
BLCA | 3 | 36534667 | 36534667 | + | Missense_Mutation | SNP | G | G | C | TCGA-E5-A4TZ-01A-11D-A31L-08 | TCGA-E5-A4TZ-10B-01D-A31J-08 | g.chr3:36534667G>C | c.712G>C | c.(712-714)Gag>Cag | p.E238Q |
BLCA | 3 | 36547283 | 36547283 | + | Silent | SNP | T | T | C | TCGA-GU-A42P-01A-11D-A23U-08 | TCGA-GU-A42P-10A-01D-A23U-08 | g.chr3:36547283T>C | c.877T>C | c.(877-879)Ttg>Ctg | p.L293L |
BLCA | 3 | 36547287 | 36547287 | + | Missense_Mutation | SNP | A | A | G | TCGA-E7-A6ME-01A-22D-A32B-08 | TCGA-E7-A6ME-10B-01D-A329-08 | g.chr3:36547287A>G | c.881A>G | c.(880-882)tAc>tGc | p.Y294C |
BLCA | 3 | 36570456 | 36570456 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr3:36570456G>C | c.1089G>C | c.(1087-1089)caG>caC | p.Q363H |
BLCA | 3 | 36587698 | 36587698 | + | Missense_Mutation | SNP | G | G | A | TCGA-2F-A9KO-01A-11D-A38G-08 | TCGA-2F-A9KO-11A-12D-A38J-08 | g.chr3:36587698G>A | c.1126G>A | c.(1126-1128)Gaa>Aaa | p.E376K |
BLCA | 3 | 36587730 | 36587730 | + | Silent | SNP | C | C | T | TCGA-DK-A3WW-01A-22D-A23M-08 | TCGA-DK-A3WW-10A-01D-A23K-08 | g.chr3:36587730C>T | c.1158C>T | c.(1156-1158)ctC>ctT | p.L386L |
BLCA | 3 | 36587764 | 36587764 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-A9RF-01A-11D-A38G-08 | TCGA-ZF-A9RF-10A-01D-A38J-08 | g.chr3:36587764G>A | c.1192G>A | c.(1192-1194)Gta>Ata | p.V398I |
BRCA | 3 | 36484914 | 36484914 | + | Missense_Mutation | SNP | C | C | T | TCGA-A2-A0CK-01A-11D-A228-09 | TCGA-A2-A0CK-10A-01D-A22A-09 | g.chr3:36484914C>T | c.170C>T | c.(169-171)gCt>gTt | p.A57V |
BRCA | 3 | 36484978 | 36484978 | + | Silent | SNP | G | G | A | TCGA-D8-A1J9-01A-11D-A13L-09 | TCGA-D8-A1J9-10A-01D-A13O-09 | g.chr3:36484978G>A | c.234G>A | c.(232-234)gaG>gaA | p.E78E |
BRCA | 3 | 36485066 | 36485066 | + | Missense_Mutation | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr3:36485066C>T | c.322C>T | c.(322-324)Cat>Tat | p.H108Y |
BRCA | 3 | 36485094 | 36485094 | + | Missense_Mutation | SNP | A | A | G | TCGA-D8-A1XL-01A-11D-A14K-09 | TCGA-D8-A1XL-10A-01D-A14K-09 | g.chr3:36485094A>G | c.350A>G | c.(349-351)aAg>aGg | p.K117R |
BRCA | 3 | 36534670 | 36534670 | + | Missense_Mutation | SNP | G | G | A | TCGA-D8-A27G-01A-11D-A16D-09 | TCGA-D8-A27G-10A-01D-A16D-09 | g.chr3:36534670G>A | c.715G>A | c.(715-717)Gaa>Aaa | p.E239K |
BRCA | 3 | 36547281 | 36547281 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-E2-A109-01A-11D-A10M-09 | TCGA-E2-A109-10A-01D-A10M-09 | g.chr3:36547281delC | c.875delC | c.(874-876)gccfs | p.A292fs |
BRCA | 3 | 36587735 | 36587735 | + | Missense_Mutation | SNP | G | G | T | TCGA-AC-A3EH-01A-22D-A228-09 | TCGA-AC-A3EH-11B-21D-A22A-09 | g.chr3:36587735G>T | c.1163G>T | c.(1162-1164)gGa>gTa | p.G388V |
CESC | 3 | 36534667 | 36534667 | + | Missense_Mutation | SNP | G | G | A | TCGA-FU-A3TQ-01A-11D-A22X-09 | TCGA-FU-A3TQ-10A-01D-A22X-09 | g.chr3:36534667G>A | c.712G>A | c.(712-714)Gag>Aag | p.E238K |
COAD | 3 | 36422209 | 36422209 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr3:36422209C>T | c.74C>T | c.(73-75)cCg>cTg | p.P25L |
COAD | 3 | 36484901 | 36484901 | + | Missense_Mutation | SNP | C | C | T | TCGA-F4-6854-01A-11D-1924-10 | TCGA-F4-6854-10A-01D-1924-10 | g.chr3:36484901C>T | c.157C>T | c.(157-159)Cgg>Tgg | p.R53W |
COAD | 3 | 36485048 | 36485048 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr3:36485048C>A | c.304C>A | c.(304-306)Cat>Aat | p.H102N |
COAD | 3 | 36485079 | 36485079 | + | Missense_Mutation | SNP | A | A | T | TCGA-A6-5656-01A-21D-1835-10 | TCGA-A6-5656-10A-01D-1835-10 | g.chr3:36485079A>T | c.335A>T | c.(334-336)gAa>gTa | p.E112V |
COAD | 3 | 36524507 | 36524507 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr3:36524507C>T | c.412C>T | c.(412-414)Cgc>Tgc | p.R138C |
COAD | 3 | 36527669 | 36527669 | + | Silent | SNP | C | C | T | TCGA-AY-4071-01A-01W-1073-09 | TCGA-AY-4071-10A-01W-1073-09 | g.chr3:36527669C>T | c.615C>T | c.(613-615)ttC>ttT | p.F205F |
COAD | 3 | 36534656 | 36534656 | + | Missense_Mutation | SNP | T | T | C | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr3:36534656T>C | c.701T>C | c.(700-702)gTg>gCg | p.V234A |
COAD | 3 | 36534691 | 36534691 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3831-01A-01W-0900-09 | TCGA-AA-3831-10A-01W-0900-09 | g.chr3:36534691G>A | c.736G>A | c.(736-738)Ggg>Agg | p.G246R |
COAD | 3 | 36534697 | 36534697 | + | Missense_Mutation | SNP | G | G | T | TCGA-AU-3779-01A-01D-1719-10 | TCGA-AU-3779-10A-01D-1719-10 | g.chr3:36534697G>T | c.742G>T | c.(742-744)Gac>Tac | p.D248Y |
COAD | 3 | 36534709 | 36534709 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr3:36534709C>T | c.754C>T | c.(754-756)Cgc>Tgc | p.R252C |
COAD | 3 | 36534709 | 36534709 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6626-01A-11D-1771-10 | TCGA-G4-6626-10A-01D-1771-10 | g.chr3:36534709C>T | c.754C>T | c.(754-756)Cgc>Tgc | p.R252C |
COAD | 3 | 36534720 | 36534720 | + | Splice_Site | SNP | C | C | T | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr3:36534720C>T | c.765C>T | c.(763-765)agC>agT | p.S255S |
COAD | 3 | 36547293 | 36547293 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr3:36547293T>G | c.887T>G | c.(886-888)tTt>tGt | p.F296C |
COAD | 3 | 36587688 | 36587688 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr3:36587688C>A | c.1116C>A | c.(1114-1116)tgC>tgA | p.C372* |
COADREAD | 3 | 36422209 | 36422209 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr3:36422209C>T | c.74C>T | c.(73-75)cCg>cTg | p.P25L |
COADREAD | 3 | 36484894 | 36484894 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:36484894G>T | c.150G>T | c.(148-150)aaG>aaT | p.K50N |
COADREAD | 3 | 36484901 | 36484901 | + | Missense_Mutation | SNP | C | C | T | TCGA-F4-6854-01A-11D-1924-10 | TCGA-F4-6854-10A-01D-1924-10 | g.chr3:36484901C>T | c.157C>T | c.(157-159)Cgg>Tgg | p.R53W |
COADREAD | 3 | 36484923 | 36484923 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-3890-01A-01W-1073-09 | TCGA-AG-3890-10A-01W-1073-09 | g.chr3:36484923T>G | c.179T>G | c.(178-180)tTc>tGc | p.F60C |
COADREAD | 3 | 36485048 | 36485048 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr3:36485048C>A | c.304C>A | c.(304-306)Cat>Aat | p.H102N |
COADREAD | 3 | 36485079 | 36485079 | + | Missense_Mutation | SNP | A | A | T | TCGA-A6-5656-01A-21D-1835-10 | TCGA-A6-5656-10A-01D-1835-10 | g.chr3:36485079A>T | c.335A>T | c.(334-336)gAa>gTa | p.E112V |
COADREAD | 3 | 36524507 | 36524507 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr3:36524507C>T | c.412C>T | c.(412-414)Cgc>Tgc | p.R138C |
COADREAD | 3 | 36527669 | 36527669 | + | Silent | SNP | C | C | T | TCGA-AY-4071-01A-01W-1073-09 | TCGA-AY-4071-10A-01W-1073-09 | g.chr3:36527669C>T | c.615C>T | c.(613-615)ttC>ttT | p.F205F |
COADREAD | 3 | 36534656 | 36534656 | + | Missense_Mutation | SNP | T | T | C | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr3:36534656T>C | c.701T>C | c.(700-702)gTg>gCg | p.V234A |
COADREAD | 3 | 36534691 | 36534691 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3831-01A-01W-0900-09 | TCGA-AA-3831-10A-01W-0900-09 | g.chr3:36534691G>A | c.736G>A | c.(736-738)Ggg>Agg | p.G246R |
COADREAD | 3 | 36534697 | 36534697 | + | Missense_Mutation | SNP | G | G | T | TCGA-AU-3779-01A-01D-1719-10 | TCGA-AU-3779-10A-01D-1719-10 | g.chr3:36534697G>T | c.742G>T | c.(742-744)Gac>Tac | p.D248Y |
COADREAD | 3 | 36534709 | 36534709 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr3:36534709C>T | c.754C>T | c.(754-756)Cgc>Tgc | p.R252C |
COADREAD | 3 | 36534709 | 36534709 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6626-01A-11D-1771-10 | TCGA-G4-6626-10A-01D-1771-10 | g.chr3:36534709C>T | c.754C>T | c.(754-756)Cgc>Tgc | p.R252C |
COADREAD | 3 | 36534720 | 36534720 | + | Splice_Site | SNP | C | C | T | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr3:36534720C>T | c.765C>T | c.(763-765)agC>agT | p.S255S |
COADREAD | 3 | 36547293 | 36547293 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr3:36547293T>G | c.887T>G | c.(886-888)tTt>tGt | p.F296C |
COADREAD | 3 | 36587685 | 36587685 | + | Silent | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:36587685C>A | c.1113C>A | c.(1111-1113)atC>atA | p.I371I |
COADREAD | 3 | 36587688 | 36587688 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr3:36587688C>A | c.1116C>A | c.(1114-1116)tgC>tgA | p.C372* |
DLBC | 3 | 36422176 | 36422176 | + | Missense_Mutation | SNP | G | G | A | TCGA-GS-A9TZ-01A-11D-A38X-10 | TCGA-GS-A9TZ-10A-01D-A38X-10 | g.chr3:36422176G>A | c.41G>A | c.(40-42)gGg>gAg | p.G14E |
ESCA | 3 | 36526484 | 36526484 | + | Missense_Mutation | SNP | C | C | T | TCGA-2H-A9GF-01A-11D-A37C-09 | TCGA-2H-A9GF-11A-11D-A37F-09 | g.chr3:36526484C>T | c.505C>T | c.(505-507)Cgt>Tgt | p.R169C |
ESCA | 3 | 36534710 | 36534710 | + | Missense_Mutation | SNP | G | G | T | TCGA-LN-A4A6-01A-11D-A27G-09 | TCGA-LN-A4A6-10A-01D-A27G-09 | g.chr3:36534710G>T | c.755G>T | c.(754-756)cGc>cTc | p.R252L |
GBMLGG | 3 | 36570431 | 36570431 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:36570431T>G | c.1064T>G | c.(1063-1065)tTc>tGc | p.F355C |
HNSC | 3 | 36524549 | 36524549 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-5441-01A-01D-1512-08 | TCGA-CV-5441-11A-01D-1512-08 | g.chr3:36524549G>A | c.454G>A | c.(454-456)Gat>Aat | p.D152N |
HNSC | 3 | 36524575 | 36524575 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A460-01A-21D-A25D-08 | TCGA-CV-A460-10A-01D-A25E-08 | g.chr3:36524575G>A | c.480G>A | c.(478-480)atG>atA | p.M160I |
HNSC | 3 | 36527664 | 36527664 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-A499-01A-11D-A24D-08 | TCGA-CN-A499-10A-01D-A24F-08 | g.chr3:36527664C>T | c.610C>T | c.(610-612)Cgc>Tgc | p.R204C |
HNSC | 3 | 36545898 | 36545898 | + | Silent | SNP | A | A | T | TCGA-F7-7848-01A-11D-2129-08 | TCGA-F7-7848-10A-01D-2129-08 | g.chr3:36545898A>T | c.780A>T | c.(778-780)ccA>ccT | p.P260P |
HNSC | 3 | 36570191 | 36570191 | + | Silent | SNP | A | A | T | TCGA-CR-7399-01A-11D-2012-08 | TCGA-CR-7399-10A-01D-2013-08 | g.chr3:36570191A>T | c.924A>T | c.(922-924)ccA>ccT | p.P308P |
HNSC | 3 | 36587704 | 36587704 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-CQ-5333-01A-01D-2394-08 | TCGA-CQ-5333-10A-01D-2394-08 | g.chr3:36587704G>T | c.1132G>T | c.(1132-1134)Gaa>Taa | p.E378* |
HNSC | 3 | 36587780 | 36587780 | + | Nonstop_Mutation | SNP | G | G | T | TCGA-CQ-A4CB-01A-11D-A25D-08 | TCGA-CQ-A4CB-10A-01D-A25E-08 | g.chr3:36587780G>T | c.1208G>T | c.(1207-1209)tGa>tTa | p.*403L |
KIPAN | 3 | 36587768 | 36587768 | + | Missense_Mutation | SNP | T | T | G | TCGA-BQ-5875-01A-11D-1589-08 | TCGA-BQ-5875-11A-01D-1589-08 | g.chr3:36587768T>G | c.1196T>G | c.(1195-1197)cTa>cGa | p.L399R |
KIRP | 3 | 36587768 | 36587768 | + | Missense_Mutation | SNP | T | T | G | TCGA-BQ-5875-01A-11D-1589-08 | TCGA-BQ-5875-11A-01D-1589-08 | g.chr3:36587768T>G | c.1196T>G | c.(1195-1197)cTa>cGa | p.L399R |
LGG | 3 | 36570431 | 36570431 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:36570431T>G | c.1064T>G | c.(1063-1065)tTc>tGc | p.F355C |
LIHC | 3 | 36485045 | 36485045 | + | Missense_Mutation | SNP | C | C | G | TCGA-RC-A6M4-01A-11D-A32G-10 | TCGA-RC-A6M4-10A-01D-A32G-10 | g.chr3:36485045C>G | c.301C>G | c.(301-303)Ctg>Gtg | p.L101V |
LIHC | 3 | 36534678 | 36534678 | + | Silent | SNP | T | T | C | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr3:36534678T>C | c.723T>C | c.(721-723)aaT>aaC | p.N241N |
LUAD | 3 | 36422206 | 36422206 | + | Missense_Mutation | SNP | A | A | T | TCGA-55-7570-01A-11D-2036-08 | TCGA-55-7570-10A-01D-2036-08 | g.chr3:36422206A>T | c.71A>T | c.(70-72)cAa>cTa | p.Q24L |
LUAD | 3 | 36422208 | 36422208 | + | Missense_Mutation | SNP | C | C | T | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr3:36422208C>T | c.73C>T | c.(73-75)Ccg>Tcg | p.P25S |
LUAD | 3 | 36484872 | 36484872 | + | Missense_Mutation | SNP | G | G | A | TCGA-50-6597-01A-11D-1855-08 | TCGA-50-6597-10A-01D-1855-08 | g.chr3:36484872G>A | c.128G>A | c.(127-129)cGa>cAa | p.R43Q |
LUAD | 3 | 36485037 | 36485037 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr3:36485037G>T | c.293G>T | c.(292-294)aGg>aTg | p.R98M |
LUAD | 3 | 36485097 | 36485097 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-7701-01A-11D-2167-08 | TCGA-86-7701-10A-01D-2167-08 | g.chr3:36485097C>A | c.353C>A | c.(352-354)cCc>cAc | p.P118H |
LUAD | 3 | 36485098 | 36485098 | + | Silent | SNP | C | C | A | TCGA-86-7701-01A-11D-2167-08 | TCGA-86-7701-10A-01D-2167-08 | g.chr3:36485098C>A | c.354C>A | c.(352-354)ccC>ccA | p.P118P |
LUAD | 3 | 36527655 | 36527655 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-50-5045-01A-01D-1625-08 | TCGA-50-5045-10A-01D-1625-08 | g.chr3:36527655G>T | c.601G>T | c.(601-603)Gag>Tag | p.E201* |
LUAD | 3 | 36527665 | 36527665 | + | Missense_Mutation | SNP | G | G | T | TCGA-73-4675-01A-01D-1265-08 | TCGA-73-4675-11A-01D-1265-08 | g.chr3:36527665G>T | c.611G>T | c.(610-612)cGc>cTc | p.R204L |
LUAD | 3 | 36545950 | 36545950 | + | Splice_Site | SNP | G | G | T | TCGA-17-Z053-01A-01W-0747-08 | TCGA-17-Z053-11A-01W-0747-08 | g.chr3:36545950G>T | | c.e7+1 | |
LUAD | 3 | 36570374 | 36570374 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr3:36570374C>T | c.1007C>T | c.(1006-1008)gCc>gTc | p.A336V |
LUSC | 3 | 36422172 | 36422172 | + | Missense_Mutation | SNP | G | G | T | TCGA-46-3769-01A-01D-0983-08 | TCGA-46-3769-10A-01D-0983-08 | g.chr3:36422172G>T | c.37G>T | c.(37-39)Gac>Tac | p.D13Y |
LUSC | 3 | 36484932 | 36484932 | + | Missense_Mutation | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr3:36484932G>A | c.188G>A | c.(187-189)cGa>cAa | p.R63Q |
LUSC | 3 | 36485038 | 36485038 | + | Missense_Mutation | SNP | G | G | T | TCGA-18-3417-01A-01D-1441-08 | TCGA-18-3417-11A-01D-1441-08 | g.chr3:36485038G>T | c.294G>T | c.(292-294)agG>agT | p.R98S |
LUSC | 3 | 36570437 | 36570437 | + | Missense_Mutation | SNP | G | G | T | TCGA-22-4601-01A-01D-1441-08 | TCGA-22-4601-11A-01D-1441-08 | g.chr3:36570437G>T | c.1070G>T | c.(1069-1071)gGg>gTg | p.G357V |
LUSC | 3 | 36587757 | 36587757 | + | Silent | SNP | C | C | A | TCGA-66-2766-01A-01D-1522-08 | TCGA-66-2766-11A-01D-1522-08 | g.chr3:36587757C>A | c.1185C>A | c.(1183-1185)ccC>ccA | p.P395P |
OV | 3 | 36534720 | 36534720 | + | Splice_Site | SNP | C | C | T | TCGA-13-1487-01A-01D-0472-08 | TCGA-13-1487-10A-01W-0545-08 | g.chr3:36534720C>T | c.765C>T | c.(763-765)agC>agT | p.S255S |
PAAD | 3 | 36547239 | 36547239 | + | Splice_Site | SNP | G | G | A | TCGA-3A-A9J0-01A-11D-A40W-08 | TCGA-3A-A9J0-10A-01D-A40W-08 | g.chr3:36547239G>A | c.833G>A | c.(832-834)gGa>gAa | p.G278E |
PRAD | 3 | 36484942 | 36484942 | + | Silent | SNP | C | C | T | TCGA-EJ-7312-01B-21D-A32B-08 | TCGA-EJ-7312-10A-01D-A329-08 | g.chr3:36484942C>T | c.198C>T | c.(196-198)agC>agT | p.S66S |
PRAD | 3 | 36485034 | 36485034 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:36485034C>T | c.290C>T | c.(289-291)gCc>gTc | p.A97V |
PRAD | 3 | 36524554 | 36524554 | + | Silent | SNP | C | C | T | TCGA-CH-5754-01A-11D-1576-08 | TCGA-CH-5754-10A-01D-1576-08 | g.chr3:36524554C>T | c.459C>T | c.(457-459)ggC>ggT | p.G153G |
PRAD | 3 | 36570362 | 36570362 | + | Missense_Mutation | SNP | G | G | T | TCGA-HC-A76W-01A-11D-A33T-08 | TCGA-HC-A76W-10A-01D-A33W-08 | g.chr3:36570362G>T | c.995G>T | c.(994-996)gGc>gTc | p.G332V |
READ | 3 | 36484894 | 36484894 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:36484894G>T | c.150G>T | c.(148-150)aaG>aaT | p.K50N |
READ | 3 | 36484923 | 36484923 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-3890-01A-01W-1073-09 | TCGA-AG-3890-10A-01W-1073-09 | g.chr3:36484923T>G | c.179T>G | c.(178-180)tTc>tGc | p.F60C |
READ | 3 | 36587685 | 36587685 | + | Silent | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:36587685C>A | c.1113C>A | c.(1111-1113)atC>atA | p.I371I |
SARC | 3 | 36570342 | 36570342 | + | Silent | SNP | G | G | A | TCGA-DX-AB2E-01A-11D-A38Z-09 | TCGA-DX-AB2E-10A-01D-A38Z-09 | g.chr3:36570342G>A | c.975G>A | c.(973-975)ggG>ggA | p.G325G |
SKCM | 3 | 36422171 | 36422171 | + | Silent | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr3:36422171G>A | c.36G>A | c.(34-36)gtG>gtA | p.V12V |
SKCM | 3 | 36422186 | 36422186 | + | Silent | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr3:36422186G>A | c.51G>A | c.(49-51)aaG>aaA | p.K17K |
SKCM | 3 | 36422196 | 36422196 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A5GS-06A-11D-A27K-08 | TCGA-D3-A5GS-10A-01D-A27N-08 | g.chr3:36422196G>A | c.61G>A | c.(61-63)Ggc>Agc | p.G21S |
SKCM | 3 | 36484943 | 36484943 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr3:36484943G>A | c.199G>A | c.(199-201)Gaa>Aaa | p.E67K |
SKCM | 3 | 36484998 | 36484998 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr3:36484998C>T | c.254C>T | c.(253-255)cCa>cTa | p.P85L |
SKCM | 3 | 36524562 | 36524562 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:36524562C>T | c.467C>T | c.(466-468)cCc>cTc | p.P156L |
SKCM | 3 | 36526476 | 36526476 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GU-06A-11D-A196-08 | TCGA-EE-A2GU-10A-01D-A198-08 | g.chr3:36526476G>A | c.497G>A | c.(496-498)gGg>gAg | p.G166E |
SKCM | 3 | 36527669 | 36527669 | + | Silent | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr3:36527669C>T | c.615C>T | c.(613-615)ttC>ttT | p.F205F |
SKCM | 3 | 36545914 | 36545914 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr3:36545914G>A | c.796G>A | c.(796-798)Gat>Aat | p.D266N |
SKCM | 3 | 36545919 | 36545919 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZC-06A-11D-A197-08 | TCGA-FS-A1ZC-10A-01D-A199-08 | g.chr3:36545919C>T | c.801C>T | c.(799-801)ttC>ttT | p.F267F |
SKCM | 3 | 36545950 | 36545950 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr3:36545950G>A | | c.e7+1 | |
SKCM | 3 | 36547238 | 36547238 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr3:36547238G>A | c.832G>A | c.(832-834)Gga>Aga | p.G278R |
SKCM | 3 | 36547239 | 36547239 | + | Splice_Site | SNP | G | G | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr3:36547239G>T | c.833G>T | c.(832-834)gGa>gTa | p.G278V |
SKCM | 3 | 36547319 | 36547319 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr3:36547319G>A | c.913G>A | c.(913-915)Gaa>Aaa | p.E305K |
SKCM | 3 | 36570342 | 36570342 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:36570342G>A | c.975G>A | c.(973-975)ggG>ggA | p.G325G |
SKCM | 3 | 36570349 | 36570349 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D3-A1Q5-06A-11D-A196-08 | TCGA-D3-A1Q5-10A-01D-A198-08 | g.chr3:36570349C>T | c.982C>T | c.(982-984)Caa>Taa | p.Q328* |
SKCM | 3 | 36570432 | 36570432 | + | Silent | SNP | C | C | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr3:36570432C>T | c.1065C>T | c.(1063-1065)ttC>ttT | p.F355F |
SKCM | 3 | 36587747 | 36587747 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr3:36587747G>A | c.1175G>A | c.(1174-1176)gGc>gAc | p.G392D |
SKCM | 3 | 36587754 | 36587754 | + | Silent | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr3:36587754C>T | c.1182C>T | c.(1180-1182)atC>atT | p.I394I |