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 | 1 | 235904873 | 235904873 | + | Missense_Mutation | SNP | C | C | G | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr1:235904873C>G | c.8207G>C | c.(8206-8208)tGt>tCt | p.C2736S |
ACC | 1 | 235966313 | 235966313 | + | Missense_Mutation | SNP | C | C | G | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr1:235966313C>G | c.3607G>C | c.(3607-3609)Gaa>Caa | p.E1203Q |
ACC | 1 | 235972428 | 235972428 | + | Missense_Mutation | SNP | C | C | A | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr1:235972428C>A | c.1690G>T | c.(1690-1692)Gct>Tct | p.A564S |
ACC | 1 | 235973763 | 235973763 | + | Missense_Mutation | SNP | G | G | C | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr1:235973763G>C | c.355C>G | c.(355-357)Cag>Gag | p.Q119E |
BLCA | 1 | 235826288 | 235826288 | + | Silent | SNP | C | C | T | TCGA-K4-A3WU-01B-11D-A23M-08 | TCGA-K4-A3WU-10A-01D-A23K-08 | g.chr1:235826288C>T | c.11358G>A | c.(11356-11358)ttG>ttA | p.L3786L |
BLCA | 1 | 235827817 | 235827817 | + | Missense_Mutation | SNP | C | C | G | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr1:235827817C>G | c.11143G>C | c.(11143-11145)Gag>Cag | p.E3715Q |
BLCA | 1 | 235884050 | 235884050 | + | Silent | SNP | G | G | A | TCGA-BT-A42C-01A-11D-A23M-08 | TCGA-BT-A42C-10A-01D-A23K-08 | g.chr1:235884050G>A | c.9471C>T | c.(9469-9471)ttC>ttT | p.F3157F |
BLCA | 1 | 235884083 | 235884083 | + | Silent | SNP | C | C | T | TCGA-XF-A9SG-01A-12D-A42E-08 | TCGA-XF-A9SG-10A-01D-A42H-08 | g.chr1:235884083C>T | c.9438G>A | c.(9436-9438)ttG>ttA | p.L3146L |
BLCA | 1 | 235884187 | 235884187 | + | Missense_Mutation | SNP | G | G | C | TCGA-FT-A3EE-01A-11D-A202-08 | TCGA-FT-A3EE-10A-01D-A202-08 | g.chr1:235884187G>C | c.9334C>G | c.(9334-9336)Cac>Gac | p.H3112D |
BLCA | 1 | 235887452 | 235887452 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr1:235887452G>T | c.9191C>A | c.(9190-9192)tCa>tAa | p.S3064* |
BLCA | 1 | 235887453 | 235887453 | + | Missense_Mutation | SNP | A | A | T | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr1:235887453A>T | c.9190T>A | c.(9190-9192)Tca>Aca | p.S3064T |
BLCA | 1 | 235892949 | 235892949 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A3SS-01A-12D-A22Z-08 | TCGA-FD-A3SS-10A-01D-A22Z-08 | g.chr1:235892949C>T | c.9053G>A | c.(9052-9054)cGa>cAa | p.R3018Q |
BLCA | 1 | 235894422 | 235894422 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A3IN-01A-11D-A20D-08 | TCGA-DK-A3IN-10A-01D-A20D-08 | g.chr1:235894422C>T | c.8857G>A | c.(8857-8859)Gaa>Aaa | p.E2953K |
BLCA | 1 | 235904826 | 235904826 | + | Missense_Mutation | SNP | A | A | C | TCGA-FT-A61P-01A-11D-A30E-08 | TCGA-FT-A61P-10A-01D-A30H-08 | g.chr1:235904826A>C | c.8254T>G | c.(8254-8256)Ttg>Gtg | p.L2752V |
BLCA | 1 | 235907429 | 235907429 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A3B5-01A-11D-A20D-08 | TCGA-FD-A3B5-10A-01D-A20D-08 | g.chr1:235907429C>G | c.8001G>C | c.(7999-8001)ttG>ttC | p.L2667F |
BLCA | 1 | 235907458 | 235907458 | + | Splice_Site | SNP | C | C | G | TCGA-FD-A3B5-01A-11D-A20D-08 | TCGA-FD-A3B5-10A-01D-A20D-08 | g.chr1:235907458C>G | | c.e30-1 | |
BLCA | 1 | 235915462 | 235915462 | + | Missense_Mutation | SNP | C | C | T | TCGA-S5-A6DX-01A-11D-A31L-08 | TCGA-S5-A6DX-10A-01D-A31J-08 | g.chr1:235915462C>T | c.7470G>A | c.(7468-7470)atG>atA | p.M2490I |
BLCA | 1 | 235920623 | 235920623 | + | Silent | SNP | G | G | A | TCGA-DK-A2I4-01A-11D-A21A-08 | TCGA-DK-A2I4-10A-01D-A21A-08 | g.chr1:235920623G>A | c.7017C>T | c.(7015-7017)ctC>ctT | p.L2339L |
BLCA | 1 | 235920751 | 235920751 | + | Missense_Mutation | SNP | C | C | T | TCGA-UY-A9PH-01A-11D-A38G-08 | TCGA-UY-A9PH-10A-01D-A38J-08 | g.chr1:235920751C>T | c.6889G>A | c.(6889-6891)Gaa>Aaa | p.E2297K |
BLCA | 1 | 235922510 | 235922510 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A2I1-01A-11D-A17V-08 | TCGA-DK-A2I1-10A-01D-A17V-08 | g.chr1:235922510C>T | c.6643G>A | c.(6643-6645)Gat>Aat | p.D2215N |
BLCA | 1 | 235922785 | 235922785 | + | Missense_Mutation | SNP | C | C | T | TCGA-R3-A69X-01A-22D-A30E-08 | TCGA-R3-A69X-10A-01D-A30H-08 | g.chr1:235922785C>T | c.6368G>A | c.(6367-6369)gGa>gAa | p.G2123E |
BLCA | 1 | 235922848 | 235922848 | + | Missense_Mutation | SNP | C | C | T | TCGA-GV-A3JV-01A-11D-A21Z-08 | TCGA-GV-A3JV-10B-01D-A21Z-08 | g.chr1:235922848C>T | c.6305G>A | c.(6304-6306)cGt>cAt | p.R2102H |
BLCA | 1 | 235929543 | 235929543 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A3PH-01A-11D-A21Z-08 | TCGA-BT-A3PH-10A-01D-A21Z-08 | g.chr1:235929543C>T | c.5957G>A | c.(5956-5958)cGa>cAa | p.R1986Q |
BLCA | 1 | 235940493 | 235940493 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-DK-AA6P-01A-11D-A391-08 | TCGA-DK-AA6P-10A-01D-A394-08 | g.chr1:235940493G>C | c.5330C>G | c.(5329-5331)tCa>tGa | p.S1777* |
BLCA | 1 | 235940598 | 235940598 | + | Missense_Mutation | SNP | G | G | A | TCGA-UY-A78O-01A-12D-A339-08 | TCGA-UY-A78O-10A-01D-A339-08 | g.chr1:235940598G>A | c.5225C>T | c.(5224-5226)tCa>tTa | p.S1742L |
BLCA | 1 | 235952011 | 235952011 | + | Missense_Mutation | SNP | G | G | C | TCGA-GC-A3RB-01A-12D-A21Z-08 | TCGA-GC-A3RB-10A-01D-A21Z-08 | g.chr1:235952011G>C | c.4678C>G | c.(4678-4680)Ctt>Gtt | p.L1560V |
BLCA | 1 | 235952067 | 235952067 | + | Missense_Mutation | SNP | G | G | A | TCGA-G2-A2EK-01A-22D-A18F-08 | TCGA-G2-A2EK-10A-01D-A18F-08 | g.chr1:235952067G>A | c.4622C>T | c.(4621-4623)tCa>tTa | p.S1541L |
BLCA | 1 | 235952110 | 235952110 | + | Missense_Mutation | SNP | G | G | C | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr1:235952110G>C | c.4579C>G | c.(4579-4581)Cct>Gct | p.P1527A |
BLCA | 1 | 235956879 | 235956879 | + | Missense_Mutation | SNP | G | G | C | TCGA-S5-AA26-01A-11D-A38G-08 | TCGA-S5-AA26-10A-01D-A38J-08 | g.chr1:235956879G>C | c.4040C>G | c.(4039-4041)tCt>tGt | p.S1347C |
BLCA | 1 | 235964228 | 235964228 | + | Silent | SNP | C | C | T | TCGA-GV-A3QI-01A-11D-A21Z-08 | TCGA-GV-A3QI-10A-01D-A21Z-08 | g.chr1:235964228C>T | c.3882G>A | c.(3880-3882)gaG>gaA | p.E1294E |
BLCA | 1 | 235966211 | 235966211 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1AG-01A-11D-A13W-08 | TCGA-DK-A1AG-10A-01D-A13W-08 | g.chr1:235966211C>T | c.3709G>A | c.(3709-3711)Gat>Aat | p.D1237N |
BLCA | 1 | 235967904 | 235967904 | + | Missense_Mutation | SNP | A | A | G | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr1:235967904A>G | c.3455T>C | c.(3454-3456)aTt>aCt | p.I1152T |
BLCA | 1 | 235969280 | 235969280 | + | Silent | SNP | T | T | C | TCGA-E7-A6ME-01A-22D-A32B-08 | TCGA-E7-A6ME-10B-01D-A329-08 | g.chr1:235969280T>C | c.3156A>G | c.(3154-3156)ctA>ctG | p.L1052L |
BLCA | 1 | 235969730 | 235969730 | + | Silent | SNP | G | G | C | TCGA-GC-A3YS-01A-11D-A23M-08 | TCGA-GC-A3YS-10A-01D-A23K-08 | g.chr1:235969730G>C | c.2706C>G | c.(2704-2706)ctC>ctG | p.L902L |
BLCA | 1 | 235969823 | 235969823 | + | Silent | SNP | G | G | A | TCGA-DK-A3IU-01A-11D-A20D-08 | TCGA-DK-A3IU-10A-01D-A20D-08 | g.chr1:235969823G>A | c.2613C>T | c.(2611-2613)ctC>ctT | p.L871L |
BLCA | 1 | 235971786 | 235971786 | + | Missense_Mutation | SNP | C | C | A | TCGA-E7-A677-01A-11D-A30E-08 | TCGA-E7-A677-10A-01D-A30H-08 | g.chr1:235971786C>A | c.2332G>T | c.(2332-2334)Gta>Tta | p.V778L |
BLCA | 1 | 235972029 | 235972029 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-BT-A20O-01A-21D-A14W-08 | TCGA-BT-A20O-11A-11D-A14W-08 | g.chr1:235972029G>A | c.2089C>T | c.(2089-2091)Cag>Tag | p.Q697* |
BLCA | 1 | 235972124 | 235972124 | + | Missense_Mutation | SNP | G | G | A | TCGA-K4-A3WU-01B-11D-A23M-08 | TCGA-K4-A3WU-10A-01D-A23K-08 | g.chr1:235972124G>A | c.1994C>T | c.(1993-1995)tCa>tTa | p.S665L |
BLCA | 1 | 235972598 | 235972598 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr1:235972598G>A | c.1520C>T | c.(1519-1521)tCt>tTt | p.S507F |
BLCA | 1 | 235972605 | 235972605 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-AA6U-01A-11D-A391-08 | TCGA-DK-AA6U-10A-01D-A394-08 | g.chr1:235972605C>G | c.1513G>C | c.(1513-1515)Gaa>Caa | p.E505Q |
BLCA | 1 | 235972637 | 235972637 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr1:235972637G>A | c.1481C>T | c.(1480-1482)tCg>tTg | p.S494L |
BLCA | 1 | 235972890 | 235972890 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-XF-A9T5-01A-11D-A42E-08 | TCGA-XF-A9T5-10A-01D-A42H-08 | g.chr1:235972890G>A | c.1228C>T | c.(1228-1230)Cag>Tag | p.Q410* |
BLCA | 1 | 235973008 | 235973008 | + | Silent | SNP | C | C | T | TCGA-DK-AA76-01A-11D-A391-08 | TCGA-DK-AA76-10A-01D-A394-08 | g.chr1:235973008C>T | c.1110G>A | c.(1108-1110)caG>caA | p.Q370Q |
BLCA | 1 | 235973317 | 235973317 | + | Silent | SNP | T | T | C | TCGA-XF-AAML-01A-11D-A42E-08 | TCGA-XF-AAML-10A-01D-A42H-08 | g.chr1:235973317T>C | c.801A>G | c.(799-801)aaA>aaG | p.K267K |
BLCA | 1 | 235973465 | 235973465 | + | Missense_Mutation | SNP | G | G | T | TCGA-DK-AA6W-01A-12D-A391-08 | TCGA-DK-AA6W-10A-01D-A394-08 | g.chr1:235973465G>T | c.653C>A | c.(652-654)gCt>gAt | p.A218D |
BLCA | 1 | 235973532 | 235973532 | + | Missense_Mutation | SNP | G | G | T | TCGA-GU-A42R-01A-11D-A23M-08 | TCGA-GU-A42R-10A-01D-A23K-08 | g.chr1:235973532G>T | c.586C>A | c.(586-588)Cct>Act | p.P196T |
BLCA | 1 | 235973621 | 235973621 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-G2-AA3D-01A-11D-A391-08 | TCGA-G2-AA3D-10A-01D-A394-08 | g.chr1:235973621G>C | c.497C>G | c.(496-498)tCa>tGa | p.S166* |
BLCA | 1 | 235973651 | 235973651 | + | Missense_Mutation | SNP | C | C | G | TCGA-CU-A3KJ-01A-11D-A21A-08 | TCGA-CU-A3KJ-10A-01D-A21A-08 | g.chr1:235973651C>G | c.467G>C | c.(466-468)aGa>aCa | p.R156T |
BLCA | 1 | 235973787 | 235973787 | + | Missense_Mutation | SNP | T | T | A | TCGA-E5-A2PC-01A-11D-A202-08 | TCGA-E5-A2PC-10B-01D-A202-08 | g.chr1:235973787T>A | c.331A>T | c.(331-333)Aac>Tac | p.N111Y |
BRCA | 1 | 235856727 | 235856727 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A18G-01A-11D-A12B-09 | TCGA-BH-A18G-10A-01D-A12B-09 | g.chr1:235856727C>T | c.10624G>A | c.(10624-10626)Gct>Act | p.A3542T |
BRCA | 1 | 235860498 | 235860498 | + | Silent | SNP | G | G | T | TCGA-AR-A256-01A-11D-A167-09 | TCGA-AR-A256-10A-01D-A167-09 | g.chr1:235860498G>T | c.10449C>A | c.(10447-10449)gtC>gtA | p.V3483V |
BRCA | 1 | 235872479 | 235872479 | + | Missense_Mutation | SNP | T | T | G | TCGA-A2-A04T-01A-21W-A050-09 | TCGA-A2-A04T-10A-01W-A055-09 | g.chr1:235872479T>G | c.10055A>C | c.(10054-10056)cAg>cCg | p.Q3352P |
BRCA | 1 | 235872544 | 235872544 | + | Silent | SNP | C | C | T | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr1:235872544C>T | c.9990G>A | c.(9988-9990)gcG>gcA | p.A3330A |
BRCA | 1 | 235872550 | 235872550 | + | Silent | SNP | A | A | C | TCGA-GM-A3NW-01A-21D-A228-09 | TCGA-GM-A3NW-10A-01D-A22A-09 | g.chr1:235872550A>C | c.9984T>G | c.(9982-9984)ccT>ccG | p.P3328P |
BRCA | 1 | 235875443 | 235875443 | + | Missense_Mutation | SNP | C | C | G | TCGA-A8-A07R-01A-21W-A050-09 | TCGA-A8-A07R-10B-01D-A047-09 | g.chr1:235875443C>G | c.9839G>C | c.(9838-9840)cGa>cCa | p.R3280P |
BRCA | 1 | 235884046 | 235884046 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr1:235884046C>T | c.9475G>A | c.(9475-9477)Gat>Aat | p.D3159N |
BRCA | 1 | 235891402 | 235891402 | + | Missense_Mutation | SNP | T | T | C | TCGA-A2-A25E-01A-11D-A167-09 | TCGA-A2-A25E-10A-01D-A167-09 | g.chr1:235891402T>C | c.9136A>G | c.(9136-9138)Aat>Gat | p.N3046D |
BRCA | 1 | 235904748 | 235904748 | + | Missense_Mutation | SNP | G | G | C | TCGA-D8-A1XK-01A-21D-A14K-09 | TCGA-D8-A1XK-10A-01D-A14K-09 | g.chr1:235904748G>C | c.8332C>G | c.(8332-8334)Cga>Gga | p.R2778G |
BRCA | 1 | 235907399 | 235907399 | + | Missense_Mutation | SNP | C | C | G | TCGA-E2-A1LH-01A-11D-A14G-09 | TCGA-E2-A1LH-11A-22D-A14G-09 | g.chr1:235907399C>G | c.8031G>C | c.(8029-8031)aaG>aaC | p.K2677N |
BRCA | 1 | 235909789 | 235909789 | + | Silent | SNP | G | G | A | TCGA-BH-A0B6-01A-11D-A19Y-09 | TCGA-BH-A0B6-10A-01D-A19Y-09 | g.chr1:235909789G>A | c.7819C>T | c.(7819-7821)Ctg>Ttg | p.L2607L |
BRCA | 1 | 235909794 | 235909794 | + | Missense_Mutation | SNP | G | G | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr1:235909794G>A | c.7814C>T | c.(7813-7815)tCg>tTg | p.S2605L |
BRCA | 1 | 235916501 | 235916501 | + | Missense_Mutation | SNP | C | C | G | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr1:235916501C>G | c.7303G>C | c.(7303-7305)Gag>Cag | p.E2435Q |
BRCA | 1 | 235922289 | 235922289 | + | Silent | SNP | T | T | A | TCGA-A7-A0DA-01A-31D-A10Y-09 | TCGA-A7-A0DA-10A-01D-A110-09 | g.chr1:235922289T>A | c.6864A>T | c.(6862-6864)cgA>cgT | p.R2288R |
BRCA | 1 | 235922292 | 235922292 | + | Missense_Mutation | SNP | G | G | T | TCGA-AC-A2FO-01A-11D-A17W-09 | TCGA-AC-A2FO-11A-12D-A17W-09 | g.chr1:235922292G>T | c.6861C>A | c.(6859-6861)aaC>aaA | p.N2287K |
BRCA | 1 | 235922444 | 235922444 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A2-A0CR-01A-11D-A228-09 | TCGA-A2-A0CR-10A-01D-A22A-09 | g.chr1:235922444G>A | c.6709C>T | c.(6709-6711)Cag>Tag | p.Q2237* |
BRCA | 1 | 235926116 | 235926116 | + | Missense_Mutation | SNP | T | T | C | TCGA-BH-A18G-01A-11D-A12B-09 | TCGA-BH-A18G-10A-01D-A12B-09 | g.chr1:235926116T>C | c.6157A>G | c.(6157-6159)Atg>Gtg | p.M2053V |
BRCA | 1 | 235929455 | 235929455 | + | Missense_Mutation | SNP | G | G | T | TCGA-BH-A5IZ-01A-11D-A27P-09 | TCGA-BH-A5IZ-11A-13D-A27P-09 | g.chr1:235929455G>T | c.6045C>A | c.(6043-6045)ttC>ttA | p.F2015L |
BRCA | 1 | 235940493 | 235940493 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-GM-A2DB-01A-31D-A19Y-09 | TCGA-GM-A2DB-10C-01D-A18P-09 | g.chr1:235940493G>C | c.5330C>G | c.(5329-5331)tCa>tGa | p.S1777* |
BRCA | 1 | 235945333 | 235945333 | + | Silent | SNP | A | A | G | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr1:235945333A>G | c.4917T>C | c.(4915-4917)tcT>tcC | p.S1639S |
BRCA | 1 | 235967816 | 235967816 | + | Silent | SNP | A | A | G | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr1:235967816A>G | c.3543T>C | c.(3541-3543)gcT>gcC | p.A1181A |
BRCA | 1 | 235969126 | 235969126 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr1:235969126G>C | c.3310C>G | c.(3310-3312)Cga>Gga | p.R1104G |
BRCA | 1 | 235969147 | 235969147 | + | Missense_Mutation | SNP | C | C | T | TCGA-D8-A27G-01A-11D-A16D-09 | TCGA-D8-A27G-10A-01D-A16D-09 | g.chr1:235969147C>T | c.3289G>A | c.(3289-3291)Gag>Aag | p.E1097K |
BRCA | 1 | 235969153 | 235969153 | + | Missense_Mutation | SNP | C | C | T | TCGA-A2-A0CT-01A-31W-A071-09 | TCGA-A2-A0CT-10A-01W-A071-09 | g.chr1:235969153C>T | c.3283G>A | c.(3283-3285)Gaa>Aaa | p.E1095K |
BRCA | 1 | 235969744 | 235969745 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr1:235969744_235969745insG | c.2691_2692insC | c.(2689-2694)acaatafs | p.I898fs |
BRCA | 1 | 235969747 | 235969748 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr1:235969747_235969748insC | c.2688_2689insG | c.(2686-2691)aacacafs | p.T897fs |
BRCA | 1 | 235969927 | 235969927 | + | Missense_Mutation | SNP | G | G | A | TCGA-AO-A03N-01B-11D-A10M-09 | TCGA-AO-A03N-10A-01D-A10M-09 | g.chr1:235969927G>A | c.2509C>T | c.(2509-2511)Cca>Tca | p.P837S |
BRCA | 1 | 235972478 | 235972478 | + | Missense_Mutation | SNP | C | C | A | TCGA-OL-A66I-01A-21D-A29N-09 | TCGA-OL-A66I-10A-01D-A29N-09 | g.chr1:235972478C>A | c.1640G>T | c.(1639-1641)tGc>tTc | p.C547F |
BRCA | 1 | 235972815 | 235972815 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr1:235972815C>A | c.1303G>T | c.(1303-1305)Gaa>Taa | p.E435* |
BRCA | 1 | 235972931 | 235972931 | + | Missense_Mutation | SNP | T | T | C | TCGA-BH-A18G-01A-11D-A12B-09 | TCGA-BH-A18G-10A-01D-A12B-09 | g.chr1:235972931T>C | c.1187A>G | c.(1186-1188)cAt>cGt | p.H396R |
BRCA | 1 | 235973301 | 235973301 | + | Missense_Mutation | SNP | C | C | T | TCGA-AO-A0JE-01A-11W-A071-09 | TCGA-AO-A0JE-10A-01W-A071-09 | g.chr1:235973301C>T | c.817G>A | c.(817-819)Gtt>Att | p.V273I |
CESC | 1 | 235850285 | 235850285 | + | Silent | SNP | G | G | A | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr1:235850285G>A | c.10764C>T | c.(10762-10764)gtC>gtT | p.V3588V |
CESC | 1 | 235944211 | 235944211 | + | Missense_Mutation | SNP | C | C | G | TCGA-IR-A3LI-01A-11D-A20U-09 | TCGA-IR-A3LI-10A-01D-A20U-09 | g.chr1:235944211C>G | c.5168G>C | c.(5167-5169)aGa>aCa | p.R1723T |
CESC | 1 | 235944340 | 235944340 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-C5-A1MH-01A-11D-A14W-08 | TCGA-C5-A1MH-10A-01D-A14W-08 | g.chr1:235944340G>C | c.5039C>G | c.(5038-5040)tCa>tGa | p.S1680* |
CESC | 1 | 235952024 | 235952024 | + | Silent | SNP | G | G | T | TCGA-RA-A741-01A-11D-A33O-09 | TCGA-RA-A741-10B-01D-A33O-09 | g.chr1:235952024G>T | c.4665C>A | c.(4663-4665)ccC>ccA | p.P1555P |
CESC | 1 | 235955247 | 235955247 | + | Missense_Mutation | SNP | G | G | A | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr1:235955247G>A | c.4295C>T | c.(4294-4296)tCa>tTa | p.S1432L |
CESC | 1 | 235964185 | 235964185 | + | Missense_Mutation | SNP | G | G | C | TCGA-IR-A3LH-01A-21D-A20U-09 | TCGA-IR-A3LH-10A-01D-A20U-09 | g.chr1:235964185G>C | c.3925C>G | c.(3925-3927)Ctg>Gtg | p.L1309V |
CESC | 1 | 235964366 | 235964366 | + | Silent | SNP | G | G | A | TCGA-IR-A3LH-01A-21D-A20U-09 | TCGA-IR-A3LH-10A-01D-A20U-09 | g.chr1:235964366G>A | c.3744C>T | c.(3742-3744)ttC>ttT | p.F1248F |
CESC | 1 | 235969198 | 235969198 | + | Missense_Mutation | SNP | C | C | G | TCGA-FU-A23K-01A-11D-A16O-08 | TCGA-FU-A23K-10A-01D-A16O-08 | g.chr1:235969198C>G | c.3238G>C | c.(3238-3240)Gct>Cct | p.A1080P |
CESC | 1 | 235969573 | 235969573 | + | Missense_Mutation | SNP | C | C | G | TCGA-FU-A23K-01A-11D-A16O-08 | TCGA-FU-A23K-10A-01D-A16O-08 | g.chr1:235969573C>G | c.2863G>C | c.(2863-2865)Gaa>Caa | p.E955Q |
CESC | 1 | 235973634 | 235973634 | + | Missense_Mutation | SNP | G | G | T | TCGA-HG-A2PA-01A-11D-A20U-09 | TCGA-HG-A2PA-10B-01D-A20U-09 | g.chr1:235973634G>T | c.484C>A | c.(484-486)Cag>Aag | p.Q162K |
CHOL | 1 | 235827341 | 235827341 | + | Missense_Mutation | SNP | C | C | A | TCGA-4G-AAZO-01A-12D-A417-09 | TCGA-4G-AAZO-11A-11D-A41A-09 | g.chr1:235827341C>A | c.11210G>T | c.(11209-11211)tGg>tTg | p.W3737L |
CHOL | 1 | 235878584 | 235878584 | + | Missense_Mutation | SNP | C | C | T | TCGA-4G-AAZO-01A-12D-A417-09 | TCGA-4G-AAZO-11A-11D-A41A-09 | g.chr1:235878584C>T | c.9701G>A | c.(9700-9702)gGc>gAc | p.G3234D |
CHOL | 1 | 235972607 | 235972607 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZH-A8Y6-01A-11D-A417-09 | TCGA-ZH-A8Y6-10A-01D-A41A-09 | g.chr1:235972607C>T | c.1511G>A | c.(1510-1512)tGt>tAt | p.C504Y |
COAD | 1 | 235826347 | 235826347 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A02W-01A-01W-A00E-09 | TCGA-AA-A02W-10A-01W-A00E-09 | g.chr1:235826347A>G | c.11299T>C | c.(11299-11301)Tac>Cac | p.Y3767H |
COAD | 1 | 235827874 | 235827874 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr1:235827874C>T | c.11086G>A | c.(11086-11088)Gtt>Att | p.V3696I |
COAD | 1 | 235850345 | 235850345 | + | Silent | SNP | C | C | G | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr1:235850345C>G | c.10704G>C | c.(10702-10704)gtG>gtC | p.V3568V |
COAD | 1 | 235856654 | 235856654 | + | Missense_Mutation | SNP | T | T | C | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr1:235856654T>C | c.10697A>G | c.(10696-10698)tAc>tGc | p.Y3566C |
COAD | 1 | 235860531 | 235860531 | + | Silent | SNP | G | G | A | TCGA-AD-6899-01A-11D-1924-10 | TCGA-AD-6899-10A-01D-1924-10 | g.chr1:235860531G>A | c.10416C>T | c.(10414-10416)taC>taT | p.Y3472Y |
COAD | 1 | 235860557 | 235860557 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr1:235860557T>C | c.10390A>G | c.(10390-10392)Ata>Gta | p.I3464V |
COAD | 1 | 235860568 | 235860568 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:235860568G>T | c.10379C>A | c.(10378-10380)cCt>cAt | p.P3460H |
COAD | 1 | 235884035 | 235884035 | + | Silent | SNP | C | C | T | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr1:235884035C>T | c.9486G>A | c.(9484-9486)caG>caA | p.Q3162Q |
COAD | 1 | 235884036 | 235884036 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-6652-01A-11D-1771-10 | TCGA-A6-6652-10A-01D-1771-10 | g.chr1:235884036T>C | c.9485A>G | c.(9484-9486)cAg>cGg | p.Q3162R |
COAD | 1 | 235884036 | 235884036 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr1:235884036T>C | c.9485A>G | c.(9484-9486)cAg>cGg | p.Q3162R |
COAD | 1 | 235884036 | 235884036 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr1:235884036T>C | c.9485A>G | c.(9484-9486)cAg>cGg | p.Q3162R |
COAD | 1 | 235884037 | 235884037 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A6-5666-01A-01D-1650-10 | TCGA-A6-5666-10A-01D-1650-10 | g.chr1:235884037G>A | c.9484C>T | c.(9484-9486)Cag>Tag | p.Q3162* |
COAD | 1 | 235884060 | 235884060 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr1:235884060C>T | c.9461G>A | c.(9460-9462)gGc>gAc | p.G3154D |
COAD | 1 | 235884120 | 235884120 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-AD-6888-01A-11D-1924-10 | TCGA-AD-6888-10A-01D-1924-10 | g.chr1:235884120A>C | c.9401T>G | c.(9400-9402)tTa>tGa | p.L3134* |
COAD | 1 | 235884128 | 235884128 | + | Silent | SNP | C | C | G | TCGA-AA-3526-01A-02W-0831-10 | TCGA-AA-3526-10A-01W-0831-10 | g.chr1:235884128C>G | c.9393G>C | c.(9391-9393)ctG>ctC | p.L3131L |
COAD | 1 | 235887410 | 235887410 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00A-01A-01W-A005-10 | TCGA-AA-A00A-10A-01W-A005-10 | g.chr1:235887410C>T | c.9233G>A | c.(9232-9234)cGt>cAt | p.R3078H |
COAD | 1 | 235897871 | 235897871 | + | Missense_Mutation | SNP | A | A | G | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr1:235897871A>G | c.8447T>C | c.(8446-8448)cTg>cCg | p.L2816P |
COAD | 1 | 235907315 | 235907315 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr1:235907315A>C | c.8115T>G | c.(8113-8115)atT>atG | p.I2705M |
COAD | 1 | 235920637 | 235920637 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr1:235920637T>C | c.7003A>G | c.(7003-7005)Aca>Gca | p.T2335A |
COAD | 1 | 235922642 | 235922642 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr1:235922642C>T | c.6511G>A | c.(6511-6513)Gca>Aca | p.A2171T |
COAD | 1 | 235922694 | 235922694 | + | Silent | SNP | G | G | A | TCGA-AA-3554-01A-01W-0833-10 | TCGA-AA-3554-10A-01W-0833-10 | g.chr1:235922694G>A | c.6459C>T | c.(6457-6459)tcC>tcT | p.S2153S |
COAD | 1 | 235922805 | 235922805 | + | Silent | SNP | C | C | T | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr1:235922805C>T | c.6348G>A | c.(6346-6348)acG>acA | p.T2116T |
COAD | 1 | 235938333 | 235938333 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-5662-01A-01D-1650-10 | TCGA-A6-5662-10A-01D-1650-10 | g.chr1:235938333T>C | c.5514A>G | c.(5512-5514)atA>atG | p.I1838M |
COAD | 1 | 235938333 | 235938333 | + | Silent | SNP | T | T | G | TCGA-D5-5539-01A-01D-1650-10 | TCGA-D5-5539-10A-01D-1650-10 | g.chr1:235938333T>G | c.5514A>C | c.(5512-5514)atA>atC | p.I1838I |
COAD | 1 | 235940533 | 235940533 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr1:235940533C>A | c.5290G>T | c.(5290-5292)Ggt>Tgt | p.G1764C |
COAD | 1 | 235944202 | 235944202 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:235944202A>C | c.5177T>G | c.(5176-5178)tTt>tGt | p.F1726C |
COAD | 1 | 235950518 | 235950518 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr1:235950518A>G | c.4844T>C | c.(4843-4845)aTa>aCa | p.I1615T |
COAD | 1 | 235955345 | 235955345 | + | Silent | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:235955345T>C | c.4197A>G | c.(4195-4197)ttA>ttG | p.L1399L |
COAD | 1 | 235956857 | 235956857 | + | Silent | SNP | A | A | G | TCGA-AD-6548-01A-11D-1835-10 | TCGA-AD-6548-10A-01D-1835-10 | g.chr1:235956857A>G | c.4062T>C | c.(4060-4062)tgT>tgC | p.C1354C |
COAD | 1 | 235969113 | 235969113 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr1:235969113G>A | c.3323C>T | c.(3322-3324)gCc>gTc | p.A1108V |
COAD | 1 | 235969311 | 235969311 | + | Missense_Mutation | SNP | G | G | C | TCGA-CM-6167-01A-11D-1650-10 | TCGA-CM-6167-10A-01D-1650-10 | g.chr1:235969311G>C | c.3125C>G | c.(3124-3126)gCt>gGt | p.A1042G |
COAD | 1 | 235969317 | 235969317 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr1:235969317G>T | c.3119C>A | c.(3118-3120)tCt>tAt | p.S1040Y |
COAD | 1 | 235969412 | 235969412 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr1:235969412C>A | c.3024G>T | c.(3022-3024)gaG>gaT | p.E1008D |
COAD | 1 | 235969521 | 235969521 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr1:235969521A>G | c.2915T>C | c.(2914-2916)aTg>aCg | p.M972T |
COAD | 1 | 235969825 | 235969825 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr1:235969825G>A | c.2611C>T | c.(2611-2613)Ctc>Ttc | p.L871F |
COAD | 1 | 235969925 | 235969925 | + | Silent | SNP | T | T | C | TCGA-A6-5660-01A-01D-1650-10 | TCGA-A6-5660-10A-01D-1650-10 | g.chr1:235969925T>C | c.2511A>G | c.(2509-2511)ccA>ccG | p.P837P |
COAD | 1 | 235969925 | 235969925 | + | Silent | SNP | T | T | C | TCGA-D5-5539-01A-01D-1650-10 | TCGA-D5-5539-10A-01D-1650-10 | g.chr1:235969925T>C | c.2511A>G | c.(2509-2511)ccA>ccG | p.P837P |
COAD | 1 | 235969998 | 235969998 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr1:235969998C>T | c.2438G>A | c.(2437-2439)cGa>cAa | p.R813Q |
COAD | 1 | 235969998 | 235969998 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:235969998C>T | c.2438G>A | c.(2437-2439)cGa>cAa | p.R813Q |
COAD | 1 | 235970023 | 235970023 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr1:235970023C>T | c.2413G>A | c.(2413-2415)Gaa>Aaa | p.E805K |
COAD | 1 | 235971896 | 235971896 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr1:235971896C>T | c.2222G>A | c.(2221-2223)aGa>aAa | p.R741K |
COAD | 1 | 235972015 | 235972015 | + | Silent | SNP | A | A | G | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr1:235972015A>G | c.2103T>C | c.(2101-2103)ttT>ttC | p.F701F |
COAD | 1 | 235972336 | 235972336 | + | Silent | SNP | A | A | G | TCGA-CM-6161-01A-11D-1650-10 | TCGA-CM-6161-10A-01D-1650-10 | g.chr1:235972336A>G | c.1782T>C | c.(1780-1782)ccT>ccC | p.P594P |
COAD | 1 | 235972337 | 235972337 | + | Missense_Mutation | SNP | G | G | T | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr1:235972337G>T | c.1781C>A | c.(1780-1782)cCt>cAt | p.P594H |
COAD | 1 | 235972351 | 235972351 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:235972351T>G | c.1767A>C | c.(1765-1767)aaA>aaC | p.K589N |
COAD | 1 | 235972459 | 235972459 | + | Silent | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr1:235972459A>G | c.1659T>C | c.(1657-1659)tgT>tgC | p.C553C |
COAD | 1 | 235972482 | 235972482 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr1:235972482G>A | c.1636C>T | c.(1636-1638)Cgg>Tgg | p.R546W |
COAD | 1 | 235972592 | 235972592 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:235972592A>C | c.1526T>G | c.(1525-1527)tTt>tGt | p.F509C |
COAD | 1 | 235973040 | 235973040 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr1:235973040C>T | c.1078G>A | c.(1078-1080)Gct>Act | p.A360T |
COAD | 1 | 235973062 | 235973062 | + | Missense_Mutation | SNP | A | A | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr1:235973062A>T | c.1056T>A | c.(1054-1056)aaT>aaA | p.N352K |
COAD | 1 | 235973133 | 235973133 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr1:235973133G>A | c.985C>T | c.(985-987)Cga>Tga | p.R329* |
COAD | 1 | 235973203 | 235973204 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr1:235973203_235973204insT | c.914_915insA | c.(913-915)aacfs | p.N305fs |
COAD | 1 | 235973543 | 235973543 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr1:235973543delA | c.575delT | c.(574-576)ttafs | p.L192fs |
COAD | 1 | 235973559 | 235973559 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3514-01A-02W-0831-10 | TCGA-AA-3514-10A-01W-0831-10 | g.chr1:235973559G>T | c.559C>A | c.(559-561)Ctg>Atg | p.L187M |
COADREAD | 1 | 235826273 | 235826273 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235826273G>T | c.11373C>A | c.(11371-11373)ttC>ttA | p.F3791L |
COADREAD | 1 | 235826347 | 235826347 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A02W-01A-01W-A00E-09 | TCGA-AA-A02W-10A-01W-A00E-09 | g.chr1:235826347A>G | c.11299T>C | c.(11299-11301)Tac>Cac | p.Y3767H |
COADREAD | 1 | 235827874 | 235827874 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr1:235827874C>T | c.11086G>A | c.(11086-11088)Gtt>Att | p.V3696I |
COADREAD | 1 | 235840882 | 235840882 | + | Missense_Mutation | SNP | T | T | C | TCGA-F5-6702-01A-11D-1826-10 | TCGA-F5-6702-10A-01D-1826-10 | g.chr1:235840882T>C | c.10838A>G | c.(10837-10839)tAt>tGt | p.Y3613C |
COADREAD | 1 | 235840883 | 235840883 | + | Missense_Mutation | SNP | A | A | G | TCGA-DY-A1DG-01A-11D-A152-10 | TCGA-DY-A1DG-10A-01D-A152-10 | g.chr1:235840883A>G | c.10837T>C | c.(10837-10839)Tat>Cat | p.Y3613H |
COADREAD | 1 | 235850291 | 235850291 | + | Silent | SNP | G | G | A | TCGA-DC-5337-01A-01D-1657-10 | TCGA-DC-5337-10A-01D-1657-10 | g.chr1:235850291G>A | c.10758C>T | c.(10756-10758)tgC>tgT | p.C3586C |
COADREAD | 1 | 235850345 | 235850345 | + | Silent | SNP | C | C | G | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr1:235850345C>G | c.10704G>C | c.(10702-10704)gtG>gtC | p.V3568V |
COADREAD | 1 | 235856654 | 235856654 | + | Missense_Mutation | SNP | T | T | C | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr1:235856654T>C | c.10697A>G | c.(10696-10698)tAc>tGc | p.Y3566C |
COADREAD | 1 | 235860531 | 235860531 | + | Silent | SNP | G | G | A | TCGA-AD-6899-01A-11D-1924-10 | TCGA-AD-6899-10A-01D-1924-10 | g.chr1:235860531G>A | c.10416C>T | c.(10414-10416)taC>taT | p.Y3472Y |
COADREAD | 1 | 235860557 | 235860557 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr1:235860557T>C | c.10390A>G | c.(10390-10392)Ata>Gta | p.I3464V |
COADREAD | 1 | 235860568 | 235860568 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:235860568G>T | c.10379C>A | c.(10378-10380)cCt>cAt | p.P3460H |
COADREAD | 1 | 235884035 | 235884035 | + | Silent | SNP | C | C | T | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr1:235884035C>T | c.9486G>A | c.(9484-9486)caG>caA | p.Q3162Q |
COADREAD | 1 | 235884036 | 235884036 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-6652-01A-11D-1771-10 | TCGA-A6-6652-10A-01D-1771-10 | g.chr1:235884036T>C | c.9485A>G | c.(9484-9486)cAg>cGg | p.Q3162R |
COADREAD | 1 | 235884036 | 235884036 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr1:235884036T>C | c.9485A>G | c.(9484-9486)cAg>cGg | p.Q3162R |
COADREAD | 1 | 235884036 | 235884036 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr1:235884036T>C | c.9485A>G | c.(9484-9486)cAg>cGg | p.Q3162R |
COADREAD | 1 | 235884037 | 235884037 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A6-5666-01A-01D-1650-10 | TCGA-A6-5666-10A-01D-1650-10 | g.chr1:235884037G>A | c.9484C>T | c.(9484-9486)Cag>Tag | p.Q3162* |
COADREAD | 1 | 235884060 | 235884060 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr1:235884060C>T | c.9461G>A | c.(9460-9462)gGc>gAc | p.G3154D |
COADREAD | 1 | 235884120 | 235884120 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-AD-6888-01A-11D-1924-10 | TCGA-AD-6888-10A-01D-1924-10 | g.chr1:235884120A>C | c.9401T>G | c.(9400-9402)tTa>tGa | p.L3134* |
COADREAD | 1 | 235884128 | 235884128 | + | Silent | SNP | C | C | G | TCGA-AA-3526-01A-02W-0831-10 | TCGA-AA-3526-10A-01W-0831-10 | g.chr1:235884128C>G | c.9393G>C | c.(9391-9393)ctG>ctC | p.L3131L |
COADREAD | 1 | 235887410 | 235887410 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00A-01A-01W-A005-10 | TCGA-AA-A00A-10A-01W-A005-10 | g.chr1:235887410C>T | c.9233G>A | c.(9232-9234)cGt>cAt | p.R3078H |
COADREAD | 1 | 235897871 | 235897871 | + | Missense_Mutation | SNP | A | A | G | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr1:235897871A>G | c.8447T>C | c.(8446-8448)cTg>cCg | p.L2816P |
COADREAD | 1 | 235907315 | 235907315 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr1:235907315A>C | c.8115T>G | c.(8113-8115)atT>atG | p.I2705M |
COADREAD | 1 | 235920623 | 235920623 | + | Silent | SNP | G | G | A | TCGA-AG-3890-01A-01W-1073-09 | TCGA-AG-3890-10A-01W-1073-09 | g.chr1:235920623G>A | c.7017C>T | c.(7015-7017)ctC>ctT | p.L2339L |
COADREAD | 1 | 235920637 | 235920637 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr1:235920637T>C | c.7003A>G | c.(7003-7005)Aca>Gca | p.T2335A |
COADREAD | 1 | 235922642 | 235922642 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr1:235922642C>T | c.6511G>A | c.(6511-6513)Gca>Aca | p.A2171T |
COADREAD | 1 | 235922694 | 235922694 | + | Silent | SNP | G | G | A | TCGA-AA-3554-01A-01W-0833-10 | TCGA-AA-3554-10A-01W-0833-10 | g.chr1:235922694G>A | c.6459C>T | c.(6457-6459)tcC>tcT | p.S2153S |
COADREAD | 1 | 235922805 | 235922805 | + | Silent | SNP | C | C | T | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr1:235922805C>T | c.6348G>A | c.(6346-6348)acG>acA | p.T2116T |
COADREAD | 1 | 235938333 | 235938333 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-5662-01A-01D-1650-10 | TCGA-A6-5662-10A-01D-1650-10 | g.chr1:235938333T>C | c.5514A>G | c.(5512-5514)atA>atG | p.I1838M |
COADREAD | 1 | 235938333 | 235938333 | + | Silent | SNP | T | T | G | TCGA-D5-5539-01A-01D-1650-10 | TCGA-D5-5539-10A-01D-1650-10 | g.chr1:235938333T>G | c.5514A>C | c.(5512-5514)atA>atC | p.I1838I |
COADREAD | 1 | 235938335 | 235938335 | + | Missense_Mutation | SNP | T | T | C | TCGA-DY-A0XA-01A-11D-A152-10 | TCGA-DY-A0XA-10A-01D-A152-10 | g.chr1:235938335T>C | c.5512A>G | c.(5512-5514)Ata>Gta | p.I1838V |
COADREAD | 1 | 235940533 | 235940533 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr1:235940533C>A | c.5290G>T | c.(5290-5292)Ggt>Tgt | p.G1764C |
COADREAD | 1 | 235944202 | 235944202 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:235944202A>C | c.5177T>G | c.(5176-5178)tTt>tGt | p.F1726C |
COADREAD | 1 | 235950518 | 235950518 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr1:235950518A>G | c.4844T>C | c.(4843-4845)aTa>aCa | p.I1615T |
COADREAD | 1 | 235955020 | 235955020 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr1:235955020C>A | c.4522G>T | c.(4522-4524)Gat>Tat | p.D1508Y |
COADREAD | 1 | 235955345 | 235955345 | + | Silent | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:235955345T>C | c.4197A>G | c.(4195-4197)ttA>ttG | p.L1399L |
COADREAD | 1 | 235956857 | 235956857 | + | Silent | SNP | A | A | G | TCGA-AD-6548-01A-11D-1835-10 | TCGA-AD-6548-10A-01D-1835-10 | g.chr1:235956857A>G | c.4062T>C | c.(4060-4062)tgT>tgC | p.C1354C |
COADREAD | 1 | 235969113 | 235969113 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr1:235969113G>A | c.3323C>T | c.(3322-3324)gCc>gTc | p.A1108V |
COADREAD | 1 | 235969311 | 235969311 | + | Missense_Mutation | SNP | G | G | C | TCGA-CM-6167-01A-11D-1650-10 | TCGA-CM-6167-10A-01D-1650-10 | g.chr1:235969311G>C | c.3125C>G | c.(3124-3126)gCt>gGt | p.A1042G |
COADREAD | 1 | 235969317 | 235969317 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr1:235969317G>T | c.3119C>A | c.(3118-3120)tCt>tAt | p.S1040Y |
COADREAD | 1 | 235969412 | 235969412 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr1:235969412C>A | c.3024G>T | c.(3022-3024)gaG>gaT | p.E1008D |
COADREAD | 1 | 235969521 | 235969521 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr1:235969521A>G | c.2915T>C | c.(2914-2916)aTg>aCg | p.M972T |
COADREAD | 1 | 235969825 | 235969825 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr1:235969825G>A | c.2611C>T | c.(2611-2613)Ctc>Ttc | p.L871F |
COADREAD | 1 | 235969925 | 235969925 | + | Silent | SNP | T | T | C | TCGA-A6-5660-01A-01D-1650-10 | TCGA-A6-5660-10A-01D-1650-10 | g.chr1:235969925T>C | c.2511A>G | c.(2509-2511)ccA>ccG | p.P837P |
COADREAD | 1 | 235969925 | 235969925 | + | Silent | SNP | T | T | C | TCGA-D5-5539-01A-01D-1650-10 | TCGA-D5-5539-10A-01D-1650-10 | g.chr1:235969925T>C | c.2511A>G | c.(2509-2511)ccA>ccG | p.P837P |
COADREAD | 1 | 235969926 | 235969926 | + | Missense_Mutation | SNP | G | G | T | TCGA-F5-6464-01A-11D-1733-10 | TCGA-F5-6464-10A-01D-1733-10 | g.chr1:235969926G>T | c.2510C>A | c.(2509-2511)cCa>cAa | p.P837Q |
COADREAD | 1 | 235969998 | 235969998 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr1:235969998C>T | c.2438G>A | c.(2437-2439)cGa>cAa | p.R813Q |
COADREAD | 1 | 235969998 | 235969998 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:235969998C>T | c.2438G>A | c.(2437-2439)cGa>cAa | p.R813Q |
COADREAD | 1 | 235970023 | 235970023 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr1:235970023C>T | c.2413G>A | c.(2413-2415)Gaa>Aaa | p.E805K |
COADREAD | 1 | 235971896 | 235971896 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr1:235971896C>T | c.2222G>A | c.(2221-2223)aGa>aAa | p.R741K |
COADREAD | 1 | 235972015 | 235972015 | + | Silent | SNP | A | A | G | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr1:235972015A>G | c.2103T>C | c.(2101-2103)ttT>ttC | p.F701F |
COADREAD | 1 | 235972336 | 235972336 | + | Silent | SNP | A | A | G | TCGA-CM-6161-01A-11D-1650-10 | TCGA-CM-6161-10A-01D-1650-10 | g.chr1:235972336A>G | c.1782T>C | c.(1780-1782)ccT>ccC | p.P594P |
COADREAD | 1 | 235972337 | 235972337 | + | Missense_Mutation | SNP | G | G | T | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr1:235972337G>T | c.1781C>A | c.(1780-1782)cCt>cAt | p.P594H |
COADREAD | 1 | 235972351 | 235972351 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr1:235972351T>G | c.1767A>C | c.(1765-1767)aaA>aaC | p.K589N |
COADREAD | 1 | 235972459 | 235972459 | + | Silent | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr1:235972459A>G | c.1659T>C | c.(1657-1659)tgT>tgC | p.C553C |
COADREAD | 1 | 235972482 | 235972482 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr1:235972482G>A | c.1636C>T | c.(1636-1638)Cgg>Tgg | p.R546W |
COADREAD | 1 | 235972592 | 235972592 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr1:235972592A>C | c.1526T>G | c.(1525-1527)tTt>tGt | p.F509C |
COADREAD | 1 | 235972610 | 235972610 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235972610C>T | c.1508G>A | c.(1507-1509)cGa>cAa | p.R503Q |
COADREAD | 1 | 235972904 | 235972904 | + | Missense_Mutation | SNP | A | A | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235972904A>G | c.1214T>C | c.(1213-1215)tTg>tCg | p.L405S |
COADREAD | 1 | 235973040 | 235973040 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr1:235973040C>T | c.1078G>A | c.(1078-1080)Gct>Act | p.A360T |
COADREAD | 1 | 235973062 | 235973062 | + | Missense_Mutation | SNP | A | A | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr1:235973062A>T | c.1056T>A | c.(1054-1056)aaT>aaA | p.N352K |
COADREAD | 1 | 235973133 | 235973133 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr1:235973133G>A | c.985C>T | c.(985-987)Cga>Tga | p.R329* |
COADREAD | 1 | 235973133 | 235973133 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235973133G>A | c.985C>T | c.(985-987)Cga>Tga | p.R329* |
COADREAD | 1 | 235973203 | 235973204 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr1:235973203_235973204insT | c.914_915insA | c.(913-915)aacfs | p.N305fs |
COADREAD | 1 | 235973543 | 235973543 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr1:235973543delA | c.575delT | c.(574-576)ttafs | p.L192fs |
COADREAD | 1 | 235973559 | 235973559 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3514-01A-02W-0831-10 | TCGA-AA-3514-10A-01W-0831-10 | g.chr1:235973559G>T | c.559C>A | c.(559-561)Ctg>Atg | p.L187M |
COADREAD | 1 | 235973720 | 235973720 | + | Missense_Mutation | SNP | A | A | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235973720A>G | c.398T>C | c.(397-399)gTt>gCt | p.V133A |
DLBC | 1 | 235887393 | 235887393 | + | Missense_Mutation | SNP | C | C | T | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr1:235887393C>T | c.9250G>A | c.(9250-9252)Gat>Aat | p.D3084N |
DLBC | 1 | 235907279 | 235907279 | + | Splice_Site | SNP | A | A | G | TCGA-G8-6907-01A-11D-2210-10 | TCGA-G8-6907-14A-01D-2210-10 | g.chr1:235907279A>G | c.8151T>C | c.(8149-8151)atT>atC | p.I2717I |
DLBC | 1 | 235918870 | 235918870 | + | Silent | SNP | T | T | G | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr1:235918870T>G | c.7137A>C | c.(7135-7137)ctA>ctC | p.L2379L |
DLBC | 1 | 235933535 | 235933535 | + | Missense_Mutation | SNP | C | C | G | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr1:235933535C>G | c.5847G>C | c.(5845-5847)caG>caC | p.Q1949H |
DLBC | 1 | 235955276 | 235955276 | + | Silent | SNP | G | G | T | TCGA-G8-6914-01A-11D-2210-10 | TCGA-G8-6914-14A-01D-2210-10 | g.chr1:235955276G>T | c.4266C>A | c.(4264-4266)gcC>gcA | p.A1422A |
DLBC | 1 | 235966354 | 235966354 | + | Missense_Mutation | SNP | G | G | C | TCGA-GS-A9TZ-01A-11D-A38X-10 | TCGA-GS-A9TZ-10A-01D-A38X-10 | g.chr1:235966354G>C | c.3566C>G | c.(3565-3567)tCt>tGt | p.S1189C |
DLBC | 1 | 235971802 | 235971802 | + | Silent | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr1:235971802G>A | c.2316C>T | c.(2314-2316)gaC>gaT | p.D772D |
ESCA | 1 | 235827307 | 235827307 | + | Silent | SNP | G | G | A | TCGA-L5-A4OU-01A-11D-A28B-09 | TCGA-L5-A4OU-11A-11D-A28E-09 | g.chr1:235827307G>A | c.11244C>T | c.(11242-11244)ccC>ccT | p.P3748P |
ESCA | 1 | 235860435 | 235860435 | + | Missense_Mutation | SNP | G | G | C | TCGA-VR-A8EP-01A-31D-A403-09 | TCGA-VR-A8EP-10B-01D-A403-09 | g.chr1:235860435G>C | c.10512C>G | c.(10510-10512)atC>atG | p.I3504M |
ESCA | 1 | 235878571 | 235878571 | + | Silent | SNP | G | G | T | TCGA-JY-A6F8-01A-11D-A33E-09 | TCGA-JY-A6F8-10A-01D-A33H-09 | g.chr1:235878571G>T | c.9714C>A | c.(9712-9714)tcC>tcA | p.S3238S |
ESCA | 1 | 235896893 | 235896893 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-L5-A8NF-01A-11D-A37C-09 | TCGA-L5-A8NF-11A-11D-A37F-09 | g.chr1:235896893delT | c.8711delA | c.(8710-8712)aagfs | p.K2904fs |
ESCA | 1 | 235897834 | 235897834 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-IG-A4P3-01A-11D-A27G-09 | TCGA-IG-A4P3-10A-01D-A27G-09 | g.chr1:235897834G>T | c.8484C>A | c.(8482-8484)tgC>tgA | p.C2828* |
ESCA | 1 | 235897834 | 235897834 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr1:235897834G>T | c.8484C>A | c.(8482-8484)tgC>tgA | p.C2828* |
ESCA | 1 | 235914600 | 235914600 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr1:235914600C>T | c.7690G>A | c.(7690-7692)Gca>Aca | p.A2564T |
ESCA | 1 | 235918868 | 235918868 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OH-01A-11D-A27G-09 | TCGA-L5-A4OH-11A-11D-A27G-09 | g.chr1:235918868G>T | c.7139C>A | c.(7138-7140)gCc>gAc | p.A2380D |
ESCA | 1 | 235922855 | 235922855 | + | Missense_Mutation | SNP | T | T | C | TCGA-LN-A4MR-01A-11D-A28B-09 | TCGA-LN-A4MR-10A-01D-A28E-09 | g.chr1:235922855T>C | c.6298A>G | c.(6298-6300)Atg>Gtg | p.M2100V |
ESCA | 1 | 235972611 | 235972611 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-S8-A6BV-01A-21D-A31U-09 | TCGA-S8-A6BV-10A-01D-A31U-09 | g.chr1:235972611G>A | c.1507C>T | c.(1507-1509)Cga>Tga | p.R503* |
ESCA | 1 | 235972743 | 235972743 | + | Missense_Mutation | SNP | C | C | G | TCGA-LN-A4A6-01A-11D-A27G-09 | TCGA-LN-A4A6-10A-01D-A27G-09 | g.chr1:235972743C>G | c.1375G>C | c.(1375-1377)Gat>Cat | p.D459H |
ESCA | 1 | 235976294 | 235976294 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A8NL-01A-12D-A37C-09 | TCGA-L5-A8NL-11A-12D-A37F-09 | g.chr1:235976294G>A | c.260C>T | c.(259-261)cCt>cTt | p.P87L |
GBM | 1 | 235860518 | 235860518 | + | Missense_Mutation | SNP | T | T | C | TCGA-12-0619-01A-01D-1492-08 | TCGA-12-0619-10A-01D-1492-08 | g.chr1:235860518T>C | c.10429A>G | c.(10429-10431)Agt>Ggt | p.S3477G |
GBM | 1 | 235866229 | 235866229 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-12-3649-01A-01D-1495-08 | TCGA-12-3649-10A-01D-1495-08 | g.chr1:235866229G>A | c.10192C>T | c.(10192-10194)Cga>Tga | p.R3398* |
GBM | 1 | 235866238 | 235866238 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-4157-01A-01D-1353-08 | TCGA-14-4157-10A-01D-1353-08 | g.chr1:235866238C>T | c.10183G>A | c.(10183-10185)Gtt>Att | p.V3395I |
GBM | 1 | 235922440 | 235922440 | + | Missense_Mutation | SNP | C | C | T | TCGA-26-5132-01A-01D-1486-08 | TCGA-26-5132-10A-01D-1486-08 | g.chr1:235922440C>T | c.6713G>A | c.(6712-6714)cGa>cAa | p.R2238Q |
GBM | 1 | 235940405 | 235940405 | + | Silent | SNP | G | G | A | TCGA-06-0214-01A-02D-1491-08 | TCGA-06-0214-10A-01D-1491-08 | g.chr1:235940405G>A | c.5418C>T | c.(5416-5418)caC>caT | p.H1806H |
GBM | 1 | 235969724 | 235969724 | + | Silent | SNP | C | C | T | TCGA-06-0168-01A-01D-1491-08 | TCGA-06-0168-10A-01D-1491-08 | g.chr1:235969724C>T | c.2712G>A | c.(2710-2712)gtG>gtA | p.V904V |
GBM | 1 | 235993676 | 235993676 | + | Silent | SNP | G | G | A | TCGA-32-1982-01A-01D-1494-08 | TCGA-32-1982-10A-01D-1494-08 | g.chr1:235993676G>A | c.42C>T | c.(40-42)acC>acT | p.T14T |
GBMLGG | 1 | 235827839 | 235827839 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235827839G>A | c.11121C>T | c.(11119-11121)tcC>tcT | p.S3707S |
GBMLGG | 1 | 235860518 | 235860518 | + | Missense_Mutation | SNP | T | T | C | TCGA-12-0619-01A-01D-1492-08 | TCGA-12-0619-10A-01D-1492-08 | g.chr1:235860518T>C | c.10429A>G | c.(10429-10431)Agt>Ggt | p.S3477G |
GBMLGG | 1 | 235866229 | 235866229 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-12-3649-01A-01D-1495-08 | TCGA-12-3649-10A-01D-1495-08 | g.chr1:235866229G>A | c.10192C>T | c.(10192-10194)Cga>Tga | p.R3398* |
GBMLGG | 1 | 235866238 | 235866238 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-4157-01A-01D-1353-08 | TCGA-14-4157-10A-01D-1353-08 | g.chr1:235866238C>T | c.10183G>A | c.(10183-10185)Gtt>Att | p.V3395I |
GBMLGG | 1 | 235922440 | 235922440 | + | Missense_Mutation | SNP | C | C | T | TCGA-26-5132-01A-01D-1486-08 | TCGA-26-5132-10A-01D-1486-08 | g.chr1:235922440C>T | c.6713G>A | c.(6712-6714)cGa>cAa | p.R2238Q |
GBMLGG | 1 | 235922652 | 235922652 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235922652G>T | c.6501C>A | c.(6499-6501)agC>agA | p.S2167R |
GBMLGG | 1 | 235922740 | 235922740 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235922740G>T | c.6413C>A | c.(6412-6414)aCt>aAt | p.T2138N |
GBMLGG | 1 | 235926125 | 235926125 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235926125G>A | c.6148C>T | c.(6148-6150)Cgg>Tgg | p.R2050W |
GBMLGG | 1 | 235929502 | 235929502 | + | Missense_Mutation | SNP | G | G | A | TCGA-QH-A6CY-01A-11D-A32B-08 | TCGA-QH-A6CY-10A-01D-A329-08 | g.chr1:235929502G>A | c.5998C>T | c.(5998-6000)Ctt>Ttt | p.L2000F |
GBMLGG | 1 | 235929518 | 235929518 | + | Silent | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235929518T>C | c.5982A>G | c.(5980-5982)aaA>aaG | p.K1994K |
GBMLGG | 1 | 235940405 | 235940405 | + | Silent | SNP | G | G | A | TCGA-06-0214-01A-02D-1491-08 | TCGA-06-0214-10A-01D-1491-08 | g.chr1:235940405G>A | c.5418C>T | c.(5416-5418)caC>caT | p.H1806H |
GBMLGG | 1 | 235950608 | 235950608 | + | Missense_Mutation | SNP | T | T | C | TCGA-S9-A6WH-01A-12D-A33T-08 | TCGA-S9-A6WH-10A-01D-A33W-08 | g.chr1:235950608T>C | c.4754A>G | c.(4753-4755)aAt>aGt | p.N1585S |
GBMLGG | 1 | 235964233 | 235964233 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-7299-01A-21D-2024-08 | TCGA-DU-7299-10A-01D-2024-08 | g.chr1:235964233A>C | c.3877T>G | c.(3877-3879)Ttt>Gtt | p.F1293V |
GBMLGG | 1 | 235969400 | 235969400 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235969400C>A | c.3036G>T | c.(3034-3036)aaG>aaT | p.K1012N |
GBMLGG | 1 | 235969487 | 235969487 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235969487C>T | c.2949G>A | c.(2947-2949)agG>agA | p.R983R |
GBMLGG | 1 | 235969724 | 235969724 | + | Silent | SNP | C | C | T | TCGA-06-0168-01A-01D-1491-08 | TCGA-06-0168-10A-01D-1491-08 | g.chr1:235969724C>T | c.2712G>A | c.(2710-2712)gtG>gtA | p.V904V |
GBMLGG | 1 | 235972444 | 235972444 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235972444C>T | c.1674G>A | c.(1672-1674)ttG>ttA | p.L558L |
GBMLGG | 1 | 235973133 | 235973133 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235973133G>A | c.985C>T | c.(985-987)Cga>Tga | p.R329* |
GBMLGG | 1 | 235993676 | 235993676 | + | Silent | SNP | G | G | A | TCGA-32-1982-01A-01D-1494-08 | TCGA-32-1982-10A-01D-1494-08 | g.chr1:235993676G>A | c.42C>T | c.(40-42)acC>acT | p.T14T |
HNSC | 1 | 235827826 | 235827826 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-6954-01A-11D-1912-08 | TCGA-CV-6954-10A-01D-1912-08 | g.chr1:235827826T>C | c.11134A>G | c.(11134-11136)Aac>Gac | p.N3712D |
HNSC | 1 | 235850334 | 235850334 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-6021-01A-11D-1683-08 | TCGA-CN-6021-10A-01D-1683-08 | g.chr1:235850334G>A | c.10715C>T | c.(10714-10716)gCt>gTt | p.A3572V |
HNSC | 1 | 235860530 | 235860530 | + | Missense_Mutation | SNP | C | C | T | TCGA-CX-7082-01A-11D-2012-08 | TCGA-CX-7082-10A-01D-2013-08 | g.chr1:235860530C>T | c.10417G>A | c.(10417-10419)Gtg>Atg | p.V3473M |
HNSC | 1 | 235866193 | 235866193 | + | Missense_Mutation | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr1:235866193T>C | c.10228A>G | c.(10228-10230)Act>Gct | p.T3410A |
HNSC | 1 | 235904812 | 235904812 | + | Silent | SNP | G | G | A | TCGA-CV-7250-01A-11D-2012-08 | TCGA-CV-7250-10A-01D-2013-08 | g.chr1:235904812G>A | c.8268C>T | c.(8266-8268)caC>caT | p.H2756H |
HNSC | 1 | 235904814 | 235904814 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-6478-01A-11D-1870-08 | TCGA-CR-6478-10A-01D-1870-08 | g.chr1:235904814G>A | c.8266C>T | c.(8266-8268)Cac>Tac | p.H2756Y |
HNSC | 1 | 235915332 | 235915332 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CR-6481-01A-11D-1870-08 | TCGA-CR-6481-10A-01D-1870-08 | g.chr1:235915332G>A | c.7600C>T | c.(7600-7602)Caa>Taa | p.Q2534* |
HNSC | 1 | 235915397 | 235915397 | + | Missense_Mutation | SNP | C | C | T | TCGA-TN-A7HL-01A-11D-A34J-08 | TCGA-TN-A7HL-10A-01D-A34M-08 | g.chr1:235915397C>T | c.7535G>A | c.(7534-7536)tGc>tAc | p.C2512Y |
HNSC | 1 | 235915445 | 235915445 | + | Missense_Mutation | SNP | A | A | G | TCGA-CN-5373-01A-01D-1434-08 | TCGA-CN-5373-10A-01D-1434-08 | g.chr1:235915445A>G | c.7487T>C | c.(7486-7488)cTt>cCt | p.L2496P |
HNSC | 1 | 235922444 | 235922444 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CQ-A4CD-01A-21D-A25D-08 | TCGA-CQ-A4CD-10A-01D-A25E-08 | g.chr1:235922444G>A | c.6709C>T | c.(6709-6711)Cag>Tag | p.Q2237* |
HNSC | 1 | 235922480 | 235922480 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-6481-01A-11D-1870-08 | TCGA-CR-6481-10A-01D-1870-08 | g.chr1:235922480G>A | c.6673C>T | c.(6673-6675)Cgc>Tgc | p.R2225C |
HNSC | 1 | 235933543 | 235933543 | + | Missense_Mutation | SNP | G | G | C | TCGA-CV-A45Q-01A-11D-A24D-08 | TCGA-CV-A45Q-10A-01D-A24F-08 | g.chr1:235933543G>C | c.5839C>G | c.(5839-5841)Cac>Gac | p.H1947D |
HNSC | 1 | 235940477 | 235940477 | + | Silent | SNP | G | G | A | TCGA-CR-7401-01A-11D-2012-08 | TCGA-CR-7401-10A-01D-2013-08 | g.chr1:235940477G>A | c.5346C>T | c.(5344-5346)agC>agT | p.S1782S |
HNSC | 1 | 235945231 | 235945231 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-A6UY-01A-12D-A34J-08 | TCGA-CN-A6UY-10B-01D-A34M-08 | g.chr1:235945231G>T | c.5019C>A | c.(5017-5019)ttC>ttA | p.F1673L |
HNSC | 1 | 235952058 | 235952058 | + | Missense_Mutation | SNP | G | G | T | TCGA-BA-7269-01A-11D-2012-08 | TCGA-BA-7269-10A-01D-2013-08 | g.chr1:235952058G>T | c.4631C>A | c.(4630-4632)tCc>tAc | p.S1544Y |
HNSC | 1 | 235964315 | 235964327 | + | Frame_Shift_Del | DEL | TTCCCCTTGAGTG | TTCCCCTTGAGTG | - | TCGA-BB-4227-01A-01D-1870-08 | TCGA-BB-4227-10A-01D-1870-08 | g.chr1:235964315_235964327delTTCCCCTTGAGTG | c.3783_3795delCACTCAAGGGGAA | c.(3781-3795)ctcactcaaggggaafs | p.LTQGE1261fs |
HNSC | 1 | 235966293 | 235966293 | + | Silent | SNP | A | A | G | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr1:235966293A>G | c.3627T>C | c.(3625-3627)tgT>tgC | p.C1209C |
HNSC | 1 | 235969554 | 235969554 | + | Missense_Mutation | SNP | G | G | C | TCGA-F7-A622-01A-11D-A28R-08 | TCGA-F7-A622-10A-01D-A28U-08 | g.chr1:235969554G>C | c.2882C>G | c.(2881-2883)gCa>gGa | p.A961G |
HNSC | 1 | 235972380 | 235972385 | + | In_Frame_Del | DEL | TGTTAT | TGTTAT | - | TCGA-CV-7177-01A-11D-2012-08 | TCGA-CV-7177-10A-01D-2013-08 | g.chr1:235972380_235972385delTGTTAT | c.1733_1738delATAACA | c.(1732-1740)cataacatt>ctt | p.578_580HNI>L |
HNSC | 1 | 235972988 | 235972988 | + | Missense_Mutation | SNP | C | C | G | TCGA-BB-4223-01A-01D-1434-08 | TCGA-BB-4223-10A-01D-1434-08 | g.chr1:235972988C>G | c.1130G>C | c.(1129-1131)aGa>aCa | p.R377T |
HNSC | 1 | 235972999 | 235972999 | + | Silent | SNP | A | A | G | TCGA-D6-6515-01A-21D-1870-08 | TCGA-D6-6515-10A-01D-1870-08 | g.chr1:235972999A>G | c.1119T>C | c.(1117-1119)ccT>ccC | p.P373P |
HNSC | 1 | 235973499 | 235973499 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-7068-01A-11D-2078-08 | TCGA-CQ-7068-10A-01D-2078-08 | g.chr1:235973499G>A | c.619C>T | c.(619-621)Cgc>Tgc | p.R207C |
HNSC | 1 | 235973763 | 235973763 | + | Missense_Mutation | SNP | G | G | T | TCGA-CQ-A4C6-01A-11D-A25D-08 | TCGA-CQ-A4C6-10A-01D-A25E-08 | g.chr1:235973763G>T | c.355C>A | c.(355-357)Cag>Aag | p.Q119K |
HNSC | 1 | 235993528 | 235993528 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-P3-A6T3-01A-11D-A34J-08 | TCGA-P3-A6T3-10A-01D-A34M-08 | g.chr1:235993528G>A | c.190C>T | c.(190-192)Cag>Tag | p.Q64* |
HNSC | 1 | 235993708 | 235993708 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-A6JO-01B-11D-A34J-08 | TCGA-CV-A6JO-10A-01D-A34M-08 | g.chr1:235993708C>T | c.10G>A | c.(10-12)Gac>Aac | p.D4N |
KICH | 1 | 235964396 | 235964396 | + | Splice_Site | SNP | C | C | T | TCGA-KL-8343-01A-11D-2310-10 | TCGA-KL-8343-11A-01D-2310-10 | g.chr1:235964396C>T | c.3714G>A | c.(3712-3714)ggG>ggA | p.G1238G |
KIPAN | 1 | 235827769 | 235827769 | + | Missense_Mutation | SNP | C | C | A | TCGA-MH-A857-01A-11D-A34Z-10 | TCGA-MH-A857-10A-01D-A34Z-10 | g.chr1:235827769C>A | c.11191G>T | c.(11191-11193)Gta>Tta | p.V3731L |
KIPAN | 1 | 235872510 | 235872510 | + | Missense_Mutation | SNP | G | G | A | TCGA-HE-A5NL-01A-11D-A26P-10 | TCGA-HE-A5NL-10A-01D-A26P-10 | g.chr1:235872510G>A | c.10024C>T | c.(10024-10026)Cgg>Tgg | p.R3342W |
KIPAN | 1 | 235884146 | 235884146 | + | Silent | SNP | A | A | G | TCGA-CZ-4865-01A-02D-1501-10 | TCGA-CZ-4865-11A-01D-1501-10 | g.chr1:235884146A>G | c.9375T>C | c.(9373-9375)taT>taC | p.Y3125Y |
KIPAN | 1 | 235884164 | 235884164 | + | Silent | SNP | G | G | A | TCGA-MH-A55Z-01A-11D-A26P-10 | TCGA-MH-A55Z-10A-01D-A26P-10 | g.chr1:235884164G>A | c.9357C>T | c.(9355-9357)ctC>ctT | p.L3119L |
KIPAN | 1 | 235894212 | 235894212 | + | Missense_Mutation | SNP | A | A | C | TCGA-B0-5088-01A-01D-1462-08 | TCGA-B0-5088-11A-01D-1462-08 | g.chr1:235894212A>C | c.8979T>G | c.(8977-8979)ttT>ttG | p.F2993L |
KIPAN | 1 | 235904811 | 235904811 | + | Missense_Mutation | SNP | C | C | T | TCGA-SX-A7SL-01A-11D-A34Z-10 | TCGA-SX-A7SL-10A-01D-A34Z-10 | g.chr1:235904811C>T | c.8269G>A | c.(8269-8271)Gct>Act | p.A2757T |
KIPAN | 1 | 235904825 | 235904825 | + | Missense_Mutation | SNP | A | A | C | TCGA-CJ-4873-01A-01D-1373-10 | TCGA-CJ-4873-11A-01D-1373-10 | g.chr1:235904825A>C | c.8255T>G | c.(8254-8256)tTg>tGg | p.L2752W |
KIPAN | 1 | 235907322 | 235907322 | + | Missense_Mutation | SNP | T | T | C | TCGA-BP-4782-01A-02D-1421-08 | TCGA-BP-4782-11A-01D-1421-08 | g.chr1:235907322T>C | c.8108A>G | c.(8107-8109)aAa>aGa | p.K2703R |
KIPAN | 1 | 235918806 | 235918806 | + | Missense_Mutation | SNP | A | A | C | TCGA-BP-5191-01A-01D-1429-08 | TCGA-BP-5191-11A-01D-1429-08 | g.chr1:235918806A>C | c.7201T>G | c.(7201-7203)Ttt>Gtt | p.F2401V |
KIPAN | 1 | 235918888 | 235918889 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CJ-4640-01A-02D-1386-10 | TCGA-CJ-4640-11A-01D-1251-10 | g.chr1:235918888_235918889insT | c.7118_7119insA | c.(7117-7119)aatfs | p.N2373fs |
KIPAN | 1 | 235922372 | 235922372 | + | Missense_Mutation | SNP | G | G | A | TCGA-A3-3322-01A-01W-0886-08 | TCGA-A3-3322-11A-01D-0966-08 | g.chr1:235922372G>A | c.6781C>T | c.(6781-6783)Cgt>Tgt | p.R2261C |
KIPAN | 1 | 235944201 | 235944201 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-BP-4976-01A-01D-1462-08 | TCGA-BP-4976-11A-01D-1462-08 | g.chr1:235944201delA | c.5178delT | c.(5176-5178)tttfs | p.F1726fs |
KIPAN | 1 | 235950642 | 235950643 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CJ-6028-01A-11D-1669-08 | TCGA-CJ-6028-11A-01D-1669-08 | g.chr1:235950642_235950643insT | c.4719_4720insA | c.(4717-4722)aaagctfs | p.A1574fs |
KIPAN | 1 | 235964396 | 235964396 | + | Splice_Site | SNP | C | C | T | TCGA-KL-8343-01A-11D-2310-10 | TCGA-KL-8343-11A-01D-2310-10 | g.chr1:235964396C>T | c.3714G>A | c.(3712-3714)ggG>ggA | p.G1238G |
KIPAN | 1 | 235969775 | 235969775 | + | Silent | SNP | C | C | T | TCGA-CJ-5672-01A-11D-1534-10 | TCGA-CJ-5672-11A-01D-1534-10 | g.chr1:235969775C>T | c.2661G>A | c.(2659-2661)aaG>aaA | p.K887K |
KIPAN | 1 | 235969849 | 235969849 | + | Missense_Mutation | SNP | C | C | T | TCGA-GL-A9DE-01A-11D-A36X-10 | TCGA-GL-A9DE-10A-01D-A370-10 | g.chr1:235969849C>T | c.2587G>A | c.(2587-2589)Gct>Act | p.A863T |
KIPAN | 1 | 235971939 | 235971939 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CZ-5452-01A-01D-1501-10 | TCGA-CZ-5452-11A-01D-1501-10 | g.chr1:235971939G>A | c.2179C>T | c.(2179-2181)Cag>Tag | p.Q727* |
KIRC | 1 | 235884146 | 235884146 | + | Silent | SNP | A | A | G | TCGA-CZ-4865-01A-02D-1501-10 | TCGA-CZ-4865-11A-01D-1501-10 | g.chr1:235884146A>G | c.9375T>C | c.(9373-9375)taT>taC | p.Y3125Y |
KIRC | 1 | 235894212 | 235894212 | + | Missense_Mutation | SNP | A | A | C | TCGA-B0-5088-01A-01D-1462-08 | TCGA-B0-5088-11A-01D-1462-08 | g.chr1:235894212A>C | c.8979T>G | c.(8977-8979)ttT>ttG | p.F2993L |
KIRC | 1 | 235904825 | 235904825 | + | Missense_Mutation | SNP | A | A | C | TCGA-CJ-4873-01A-01D-1373-10 | TCGA-CJ-4873-11A-01D-1373-10 | g.chr1:235904825A>C | c.8255T>G | c.(8254-8256)tTg>tGg | p.L2752W |
KIRC | 1 | 235907322 | 235907322 | + | Missense_Mutation | SNP | T | T | C | TCGA-BP-4782-01A-02D-1421-08 | TCGA-BP-4782-11A-01D-1421-08 | g.chr1:235907322T>C | c.8108A>G | c.(8107-8109)aAa>aGa | p.K2703R |
KIRC | 1 | 235918806 | 235918806 | + | Missense_Mutation | SNP | A | A | C | TCGA-BP-5191-01A-01D-1429-08 | TCGA-BP-5191-11A-01D-1429-08 | g.chr1:235918806A>C | c.7201T>G | c.(7201-7203)Ttt>Gtt | p.F2401V |
KIRC | 1 | 235918888 | 235918889 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CJ-4640-01A-02D-1386-10 | TCGA-CJ-4640-11A-01D-1251-10 | g.chr1:235918888_235918889insT | c.7118_7119insA | c.(7117-7119)aatfs | p.N2373fs |
KIRC | 1 | 235922372 | 235922372 | + | Missense_Mutation | SNP | G | G | A | TCGA-A3-3322-01A-01W-0886-08 | TCGA-A3-3322-11A-01D-0966-08 | g.chr1:235922372G>A | c.6781C>T | c.(6781-6783)Cgt>Tgt | p.R2261C |
KIRC | 1 | 235944201 | 235944201 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-BP-4976-01A-01D-1462-08 | TCGA-BP-4976-11A-01D-1462-08 | g.chr1:235944201delA | c.5178delT | c.(5176-5178)tttfs | p.F1726fs |
KIRC | 1 | 235950642 | 235950643 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CJ-6028-01A-11D-1669-08 | TCGA-CJ-6028-11A-01D-1669-08 | g.chr1:235950642_235950643insT | c.4719_4720insA | c.(4717-4722)aaagctfs | p.A1574fs |
KIRC | 1 | 235969775 | 235969775 | + | Silent | SNP | C | C | T | TCGA-CJ-5672-01A-11D-1534-10 | TCGA-CJ-5672-11A-01D-1534-10 | g.chr1:235969775C>T | c.2661G>A | c.(2659-2661)aaG>aaA | p.K887K |
KIRC | 1 | 235971939 | 235971939 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CZ-5452-01A-01D-1501-10 | TCGA-CZ-5452-11A-01D-1501-10 | g.chr1:235971939G>A | c.2179C>T | c.(2179-2181)Cag>Tag | p.Q727* |
KIRP | 1 | 235827769 | 235827769 | + | Missense_Mutation | SNP | C | C | A | TCGA-MH-A857-01A-11D-A34Z-10 | TCGA-MH-A857-10A-01D-A34Z-10 | g.chr1:235827769C>A | c.11191G>T | c.(11191-11193)Gta>Tta | p.V3731L |
KIRP | 1 | 235872510 | 235872510 | + | Missense_Mutation | SNP | G | G | A | TCGA-HE-A5NL-01A-11D-A26P-10 | TCGA-HE-A5NL-10A-01D-A26P-10 | g.chr1:235872510G>A | c.10024C>T | c.(10024-10026)Cgg>Tgg | p.R3342W |
KIRP | 1 | 235884164 | 235884164 | + | Silent | SNP | G | G | A | TCGA-MH-A55Z-01A-11D-A26P-10 | TCGA-MH-A55Z-10A-01D-A26P-10 | g.chr1:235884164G>A | c.9357C>T | c.(9355-9357)ctC>ctT | p.L3119L |
KIRP | 1 | 235904811 | 235904811 | + | Missense_Mutation | SNP | C | C | T | TCGA-SX-A7SL-01A-11D-A34Z-10 | TCGA-SX-A7SL-10A-01D-A34Z-10 | g.chr1:235904811C>T | c.8269G>A | c.(8269-8271)Gct>Act | p.A2757T |
KIRP | 1 | 235969849 | 235969849 | + | Missense_Mutation | SNP | C | C | T | TCGA-GL-A9DE-01A-11D-A36X-10 | TCGA-GL-A9DE-10A-01D-A370-10 | g.chr1:235969849C>T | c.2587G>A | c.(2587-2589)Gct>Act | p.A863T |
LGG | 1 | 235827839 | 235827839 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235827839G>A | c.11121C>T | c.(11119-11121)tcC>tcT | p.S3707S |
LGG | 1 | 235922652 | 235922652 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235922652G>T | c.6501C>A | c.(6499-6501)agC>agA | p.S2167R |
LGG | 1 | 235922740 | 235922740 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235922740G>T | c.6413C>A | c.(6412-6414)aCt>aAt | p.T2138N |
LGG | 1 | 235926125 | 235926125 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235926125G>A | c.6148C>T | c.(6148-6150)Cgg>Tgg | p.R2050W |
LGG | 1 | 235929502 | 235929502 | + | Missense_Mutation | SNP | G | G | A | TCGA-QH-A6CY-01A-11D-A32B-08 | TCGA-QH-A6CY-10A-01D-A329-08 | g.chr1:235929502G>A | c.5998C>T | c.(5998-6000)Ctt>Ttt | p.L2000F |
LGG | 1 | 235929518 | 235929518 | + | Silent | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235929518T>C | c.5982A>G | c.(5980-5982)aaA>aaG | p.K1994K |
LGG | 1 | 235950608 | 235950608 | + | Missense_Mutation | SNP | T | T | C | TCGA-S9-A6WH-01A-12D-A33T-08 | TCGA-S9-A6WH-10A-01D-A33W-08 | g.chr1:235950608T>C | c.4754A>G | c.(4753-4755)aAt>aGt | p.N1585S |
LGG | 1 | 235964233 | 235964233 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-7299-01A-21D-2024-08 | TCGA-DU-7299-10A-01D-2024-08 | g.chr1:235964233A>C | c.3877T>G | c.(3877-3879)Ttt>Gtt | p.F1293V |
LGG | 1 | 235969400 | 235969400 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235969400C>A | c.3036G>T | c.(3034-3036)aaG>aaT | p.K1012N |
LGG | 1 | 235969487 | 235969487 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235969487C>T | c.2949G>A | c.(2947-2949)agG>agA | p.R983R |
LGG | 1 | 235972444 | 235972444 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235972444C>T | c.1674G>A | c.(1672-1674)ttG>ttA | p.L558L |
LGG | 1 | 235973133 | 235973133 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:235973133G>A | c.985C>T | c.(985-987)Cga>Tga | p.R329* |
LIHC | 1 | 235860518 | 235860519 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr1:235860518_235860519insG | c.10428_10429insC | c.(10426-10431)cccagtfs | p.S3477fs |
LIHC | 1 | 235880039 | 235880039 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr1:235880039delT | c.9600delA | c.(9598-9600)aaafs | p.K3200fs |
LIHC | 1 | 235887447 | 235887447 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr1:235887447delA | c.9196delT | c.(9196-9198)tccfs | p.S3066fs |
LIHC | 1 | 235892901 | 235892901 | + | Missense_Mutation | SNP | A | A | G | TCGA-WX-AA44-01A-11D-A38X-10 | TCGA-WX-AA44-10A-01D-A38X-10 | g.chr1:235892901A>G | c.9101T>C | c.(9100-9102)tTa>tCa | p.L3034S |
LIHC | 1 | 235897870 | 235897870 | + | Silent | SNP | C | C | A | TCGA-DD-AADN-01A-11D-A40R-10 | TCGA-DD-AADN-10A-01D-A40U-10 | g.chr1:235897870C>A | c.8448G>T | c.(8446-8448)ctG>ctT | p.L2816L |
LIHC | 1 | 235915327 | 235915327 | + | Silent | SNP | A | A | G | TCGA-DD-A73B-01A-12D-A32G-10 | TCGA-DD-A73B-10A-01D-A32G-10 | g.chr1:235915327A>G | c.7605T>C | c.(7603-7605)aaT>aaC | p.N2535N |
LIHC | 1 | 235916449 | 235916451 | + | In_Frame_Del | DEL | AGA | AGA | - | TCGA-DD-AADR-01A-11D-A40R-10 | TCGA-DD-AADR-10A-01D-A40U-10 | g.chr1:235916449_235916451delAGA | c.7353_7355delTCT | c.(7351-7356)cttctc>ctc | p.2451_2452LL>L |
LIHC | 1 | 235922305 | 235922305 | + | Missense_Mutation | SNP | T | T | C | TCGA-BC-A10W-01A-11D-A12Z-10 | TCGA-BC-A10W-11A-11D-A12Z-10 | g.chr1:235922305T>C | c.6848A>G | c.(6847-6849)gAg>gGg | p.E2283G |
LIHC | 1 | 235922871 | 235922871 | + | Silent | SNP | T | T | C | TCGA-DD-AAE3-01A-11D-A40R-10 | TCGA-DD-AAE3-10A-01D-A40U-10 | g.chr1:235922871T>C | c.6282A>G | c.(6280-6282)caA>caG | p.Q2094Q |
LIHC | 1 | 235937265 | 235937265 | + | Missense_Mutation | SNP | T | T | A | TCGA-G3-A3CH-01A-11D-A22F-10 | TCGA-G3-A3CH-11A-11D-A22F-10 | g.chr1:235937265T>A | c.5661A>T | c.(5659-5661)gaA>gaT | p.E1887D |
LIHC | 1 | 235940366 | 235940366 | + | Silent | SNP | G | G | A | TCGA-DD-A4NH-01A-11D-A27I-10 | TCGA-DD-A4NH-10A-01D-A27I-10 | g.chr1:235940366G>A | c.5457C>T | c.(5455-5457)gcC>gcT | p.A1819A |
LIHC | 1 | 235945311 | 235945311 | + | Missense_Mutation | SNP | T | T | C | TCGA-CC-A3MB-01A-11D-A20W-10 | TCGA-CC-A3MB-10A-01D-A20W-10 | g.chr1:235945311T>C | c.4939A>G | c.(4939-4941)Atg>Gtg | p.M1647V |
LIHC | 1 | 235955183 | 235955183 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AACJ-01A-11D-A40R-10 | TCGA-DD-AACJ-10A-01D-A40U-10 | g.chr1:235955183T>C | c.4359A>G | c.(4357-4359)atA>atG | p.I1453M |
LIHC | 1 | 235955200 | 235955200 | + | Missense_Mutation | SNP | G | G | C | TCGA-RC-A7S9-01A-11D-A33Q-10 | TCGA-RC-A7S9-10A-02D-A33Q-10 | g.chr1:235955200G>C | c.4342C>G | c.(4342-4344)Ctt>Gtt | p.L1448V |
LIHC | 1 | 235964220 | 235964220 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr1:235964220delA | c.3890delT | c.(3889-3891)ttgfs | p.L1297fs |
LIHC | 1 | 235964399 | 235964399 | + | Splice_Site | SNP | T | T | A | TCGA-G3-A5SJ-01A-11D-A27I-10 | TCGA-G3-A5SJ-10A-01D-A27I-10 | g.chr1:235964399T>A | | c.e9-2 | |
LIHC | 1 | 235973623 | 235973623 | + | Silent | SNP | G | G | T | TCGA-DD-A4NQ-01A-21D-A28X-10 | TCGA-DD-A4NQ-10A-01D-A28X-10 | g.chr1:235973623G>T | c.495C>A | c.(493-495)acC>acA | p.T165T |
LUAD | 1 | 235826260 | 235826260 | + | Missense_Mutation | SNP | T | T | C | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr1:235826260T>C | c.11386A>G | c.(11386-11388)Agc>Ggc | p.S3796G |
LUAD | 1 | 235826344 | 235826344 | + | Missense_Mutation | SNP | T | T | C | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr1:235826344T>C | c.11302A>G | c.(11302-11304)Aca>Gca | p.T3768A |
LUAD | 1 | 235826359 | 235826359 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8510-01A-11D-2393-08 | TCGA-55-8510-10A-01D-2393-08 | g.chr1:235826359C>A | c.11287G>T | c.(11287-11289)Ggc>Tgc | p.G3763C |
LUAD | 1 | 235827894 | 235827894 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z049-01A-01W-0746-08 | TCGA-17-Z049-11A-01W-0747-08 | g.chr1:235827894C>A | c.11066G>T | c.(11065-11067)tGg>tTg | p.W3689L |
LUAD | 1 | 235840794 | 235840794 | + | Silent | SNP | T | T | A | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chr1:235840794T>A | c.10926A>T | c.(10924-10926)atA>atT | p.I3642I |
LUAD | 1 | 235840796 | 235840796 | + | Missense_Mutation | SNP | T | T | G | TCGA-95-8039-01A-11D-2238-08 | TCGA-95-8039-10A-01D-2238-08 | g.chr1:235840796T>G | c.10924A>C | c.(10924-10926)Ata>Cta | p.I3642L |
LUAD | 1 | 235850271 | 235850271 | + | Missense_Mutation | SNP | G | G | T | TCGA-62-8399-01A-21D-2323-08 | TCGA-62-8399-10A-01D-2323-08 | g.chr1:235850271G>T | c.10778C>A | c.(10777-10779)aCa>aAa | p.T3593K |
LUAD | 1 | 235850271 | 235850271 | + | Missense_Mutation | SNP | G | G | T | TCGA-91-6835-01A-11D-1855-08 | TCGA-91-6835-11A-01D-1855-08 | g.chr1:235850271G>T | c.10778C>A | c.(10777-10779)aCa>aAa | p.T3593K |
LUAD | 1 | 235860531 | 235860531 | + | Silent | SNP | G | G | A | TCGA-50-5941-01A-11D-1753-08 | TCGA-50-5941-10A-01D-1753-08 | g.chr1:235860531G>A | c.10416C>T | c.(10414-10416)taC>taT | p.Y3472Y |
LUAD | 1 | 235860540 | 235860540 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8089-01A-11D-2238-08 | TCGA-55-8089-10A-01D-2238-08 | g.chr1:235860540C>A | c.10407G>T | c.(10405-10407)tgG>tgT | p.W3469C |
LUAD | 1 | 235866047 | 235866047 | + | Splice_Site | SNP | C | C | G | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr1:235866047C>G | c.10374G>C | c.(10372-10374)ccG>ccC | p.P3458P |
LUAD | 1 | 235878548 | 235878548 | + | Missense_Mutation | SNP | A | A | G | TCGA-86-8674-01A-21D-2393-08 | TCGA-86-8674-10A-01D-2393-08 | g.chr1:235878548A>G | c.9737T>C | c.(9736-9738)tTc>tCc | p.F3246S |
LUAD | 1 | 235878603 | 235878603 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr1:235878603C>A | c.9682G>T | c.(9682-9684)Gtg>Ttg | p.V3228L |
LUAD | 1 | 235883977 | 235883977 | + | Missense_Mutation | SNP | C | C | G | TCGA-44-7662-01A-11D-2063-08 | TCGA-44-7662-10A-01D-2063-08 | g.chr1:235883977C>G | c.9544G>C | c.(9544-9546)Gat>Cat | p.D3182H |
LUAD | 1 | 235894397 | 235894397 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-5425-01A-02D-1625-08 | TCGA-05-5425-10A-01D-1625-08 | g.chr1:235894397C>A | c.8882G>T | c.(8881-8883)cGt>cTt | p.R2961L |
LUAD | 1 | 235896917 | 235896917 | + | Missense_Mutation | SNP | A | A | T | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr1:235896917A>T | c.8687T>A | c.(8686-8688)cTc>cAc | p.L2896H |
LUAD | 1 | 235897896 | 235897896 | + | Missense_Mutation | SNP | C | C | T | TCGA-44-A47A-01A-21D-A24D-08 | TCGA-44-A47A-10A-01D-A24F-08 | g.chr1:235897896C>T | c.8422G>A | c.(8422-8424)Gaa>Aaa | p.E2808K |
LUAD | 1 | 235904858 | 235904858 | + | Missense_Mutation | SNP | C | C | G | TCGA-17-Z015-01A-01W-0746-08 | TCGA-17-Z015-11A-01W-0746-08 | g.chr1:235904858C>G | c.8222G>C | c.(8221-8223)cGa>cCa | p.R2741P |
LUAD | 1 | 235907394 | 235907394 | + | Missense_Mutation | SNP | G | G | A | TCGA-50-6590-01A-12D-1855-08 | TCGA-50-6590-11A-01D-1855-08 | g.chr1:235907394G>A | c.8036C>T | c.(8035-8037)tCa>tTa | p.S2679L |
LUAD | 1 | 235909637 | 235909637 | + | Splice_Site | SNP | T | T | G | TCGA-MN-A4N5-01A-11D-A24P-08 | TCGA-MN-A4N5-10A-01D-A24P-08 | g.chr1:235909637T>G | c.7971A>C | c.(7969-7971)caA>caC | p.Q2657H |
LUAD | 1 | 235914598 | 235914598 | + | Silent | SNP | T | T | A | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr1:235914598T>A | c.7692A>T | c.(7690-7692)gcA>gcT | p.A2564A |
LUAD | 1 | 235915417 | 235915417 | + | Missense_Mutation | SNP | T | T | C | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr1:235915417T>C | c.7515A>G | c.(7513-7515)atA>atG | p.I2505M |
LUAD | 1 | 235918832 | 235918832 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr1:235918832A>T | c.7175T>A | c.(7174-7176)tTg>tAg | p.L2392* |
LUAD | 1 | 235918847 | 235918847 | + | Missense_Mutation | SNP | C | C | T | TCGA-91-8497-01A-11D-2393-08 | TCGA-91-8497-10A-01D-2393-08 | g.chr1:235918847C>T | c.7160G>A | c.(7159-7161)cGa>cAa | p.R2387Q |
LUAD | 1 | 235918893 | 235918893 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-44-6145-01A-11D-1753-08 | TCGA-44-6145-10A-01D-1753-08 | g.chr1:235918893T>A | c.7114A>T | c.(7114-7116)Aag>Tag | p.K2372* |
LUAD | 1 | 235918941 | 235918941 | + | Missense_Mutation | SNP | C | C | G | TCGA-93-A4JQ-01A-11D-A24P-08 | TCGA-93-A4JQ-10A-01D-A24P-08 | g.chr1:235918941C>G | c.7066G>C | c.(7066-7068)Gat>Cat | p.D2356H |
LUAD | 1 | 235922575 | 235922575 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-05-4405-01A-21D-1855-08 | TCGA-05-4405-10A-01D-1855-08 | g.chr1:235922575delC | c.6578delG | c.(6577-6579)ggafs | p.G2193fs |
LUAD | 1 | 235922757 | 235922757 | + | Missense_Mutation | SNP | T | T | A | TCGA-55-7913-01B-11D-2238-08 | TCGA-55-7913-10A-01D-2238-08 | g.chr1:235922757T>A | c.6396A>T | c.(6394-6396)ttA>ttT | p.L2132F |
LUAD | 1 | 235929473 | 235929473 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-A4P7-01A-11D-A24P-08 | TCGA-86-A4P7-10A-01D-A24P-08 | g.chr1:235929473C>G | c.6027G>C | c.(6025-6027)ttG>ttC | p.L2009F |
LUAD | 1 | 235929520 | 235929520 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr1:235929520T>A | c.5980A>T | c.(5980-5982)Aaa>Taa | p.K1994* |
LUAD | 1 | 235933492 | 235933492 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-A47A-01A-21D-A24D-08 | TCGA-44-A47A-10A-01D-A24F-08 | g.chr1:235933492G>A | c.5890C>T | c.(5890-5892)Cat>Tat | p.H1964Y |
LUAD | 1 | 235937220 | 235937220 | + | Silent | SNP | T | T | C | TCGA-78-7537-01A-11D-2063-08 | TCGA-78-7537-10A-01D-2063-08 | g.chr1:235937220T>C | c.5706A>G | c.(5704-5706)gtA>gtG | p.V1902V |
LUAD | 1 | 235938216 | 235938216 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-8585-01A-11D-2393-08 | TCGA-86-8585-10A-01D-2393-08 | g.chr1:235938216C>G | c.5631G>C | c.(5629-5631)ttG>ttC | p.L1877F |
LUAD | 1 | 235944170 | 235944170 | + | Missense_Mutation | SNP | A | A | T | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr1:235944170A>T | c.5209T>A | c.(5209-5211)Tta>Ata | p.L1737I |
LUAD | 1 | 235945360 | 235945360 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr1:235945360C>A | c.4890G>T | c.(4888-4890)atG>atT | p.M1630I |
LUAD | 1 | 235950500 | 235950500 | + | Splice_Site | SNP | C | C | A | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr1:235950500C>A | c.4862G>T | c.(4861-4863)aGg>aTg | p.R1621M |
LUAD | 1 | 235950598 | 235950598 | + | Silent | SNP | G | G | A | TCGA-49-4512-01A-21D-1855-08 | TCGA-49-4512-11A-01D-1855-08 | g.chr1:235950598G>A | c.4764C>T | c.(4762-4764)ctC>ctT | p.L1588L |
LUAD | 1 | 235955264 | 235955264 | + | Silent | SNP | C | C | T | TCGA-69-A59K-01A-11D-A25L-08 | TCGA-69-A59K-10A-01D-A25L-08 | g.chr1:235955264C>T | c.4278G>A | c.(4276-4278)ttG>ttA | p.L1426L |
LUAD | 1 | 235956906 | 235956906 | + | Missense_Mutation | SNP | T | T | G | TCGA-55-8299-01A-11D-2284-08 | TCGA-55-8299-10B-01D-2323-08 | g.chr1:235956906T>G | c.4013A>C | c.(4012-4014)cAg>cCg | p.Q1338P |
LUAD | 1 | 235967931 | 235967931 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-7995-01A-11D-2184-08 | TCGA-55-7995-10A-01D-2184-08 | g.chr1:235967931C>A | c.3428G>T | c.(3427-3429)aGg>aTg | p.R1143M |
LUAD | 1 | 235969162 | 235969162 | + | Missense_Mutation | SNP | T | T | C | TCGA-49-6767-01A-11D-1855-08 | TCGA-49-6767-11A-01D-1855-08 | g.chr1:235969162T>C | c.3274A>G | c.(3274-3276)Aca>Gca | p.T1092A |
LUAD | 1 | 235969330 | 235969330 | + | Missense_Mutation | SNP | C | C | T | TCGA-MP-A4TA-01A-21D-A24P-08 | TCGA-MP-A4TA-10A-01D-A24P-08 | g.chr1:235969330C>T | c.3106G>A | c.(3106-3108)Gaa>Aaa | p.E1036K |
LUAD | 1 | 235969372 | 235969372 | + | Missense_Mutation | SNP | G | G | T | TCGA-64-5778-01A-01D-1625-08 | TCGA-64-5778-10A-01D-1625-08 | g.chr1:235969372G>T | c.3064C>A | c.(3064-3066)Cag>Aag | p.Q1022K |
LUAD | 1 | 235969480 | 235969480 | + | Missense_Mutation | SNP | C | C | T | TCGA-80-5611-01A-01D-1625-08 | TCGA-80-5611-10A-01D-1625-08 | g.chr1:235969480C>T | c.2956G>A | c.(2956-2958)Ggt>Agt | p.G986S |
LUAD | 1 | 235969542 | 235969542 | + | Missense_Mutation | SNP | G | G | C | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr1:235969542G>C | c.2894C>G | c.(2893-2895)tCt>tGt | p.S965C |
LUAD | 1 | 235969785 | 235969785 | + | Missense_Mutation | SNP | T | T | C | TCGA-50-5049-01A-01D-1625-08 | TCGA-50-5049-10A-01D-1625-08 | g.chr1:235969785T>C | c.2651A>G | c.(2650-2652)aAg>aGg | p.K884R |
LUAD | 1 | 235969806 | 235969806 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-5428-01A-01D-1625-08 | TCGA-05-5428-10A-01D-1625-08 | g.chr1:235969806C>A | c.2630G>T | c.(2629-2631)gGc>gTc | p.G877V |
LUAD | 1 | 235970013 | 235970013 | + | Missense_Mutation | SNP | C | C | T | TCGA-17-Z020-01A-01W-0746-08 | TCGA-17-Z020-11A-01W-0746-08 | g.chr1:235970013C>T | c.2423G>A | c.(2422-2424)tGc>tAc | p.C808Y |
LUAD | 1 | 235971799 | 235971799 | + | Silent | SNP | C | C | G | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr1:235971799C>G | c.2319G>C | c.(2317-2319)gtG>gtC | p.V773V |
LUAD | 1 | 235972070 | 235972070 | + | Missense_Mutation | SNP | G | G | C | TCGA-49-4514-01A-21D-1855-08 | TCGA-49-4514-11A-01D-1855-08 | g.chr1:235972070G>C | c.2048C>G | c.(2047-2049)tCt>tGt | p.S683C |
LUAD | 1 | 235972212 | 235972212 | + | Missense_Mutation | SNP | C | C | G | TCGA-17-Z045-01A-01W-0746-08 | TCGA-17-Z045-11A-01W-0747-08 | g.chr1:235972212C>G | c.1906G>C | c.(1906-1908)Gct>Cct | p.A636P |
LUAD | 1 | 235972423 | 235972423 | + | Silent | SNP | G | G | A | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr1:235972423G>A | c.1695C>T | c.(1693-1695)tcC>tcT | p.S565S |
LUAD | 1 | 235973040 | 235973040 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chr1:235973040C>A | c.1078G>T | c.(1078-1080)Gct>Tct | p.A360S |
LUAD | 1 | 235973322 | 235973322 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-7913-01B-11D-2238-08 | TCGA-55-7913-10A-01D-2238-08 | g.chr1:235973322C>G | c.796G>C | c.(796-798)Gaa>Caa | p.E266Q |
LUAD | 1 | 235973489 | 235973489 | + | Missense_Mutation | SNP | G | G | A | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr1:235973489G>A | c.629C>T | c.(628-630)aCc>aTc | p.T210I |
LUAD | 1 | 235973558 | 235973558 | + | Missense_Mutation | SNP | A | A | G | TCGA-17-Z021-01A-01W-0746-08 | TCGA-17-Z021-11A-01W-0746-08 | g.chr1:235973558A>G | c.560T>C | c.(559-561)cTg>cCg | p.L187P |
LUAD | 1 | 235973570 | 235973570 | + | Missense_Mutation | SNP | C | C | G | TCGA-MP-A4SV-01A-11D-A24P-08 | TCGA-MP-A4SV-10A-01D-A24P-08 | g.chr1:235973570C>G | c.548G>C | c.(547-549)aGa>aCa | p.R183T |
LUAD | 1 | 235973688 | 235973688 | + | Missense_Mutation | SNP | T | T | C | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr1:235973688T>C | c.430A>G | c.(430-432)Aga>Gga | p.R144G |
LUAD | 1 | 235976294 | 235976294 | + | Missense_Mutation | SNP | G | G | A | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr1:235976294G>A | c.260C>T | c.(259-261)cCt>cTt | p.P87L |
LUAD | 1 | 235993607 | 235993607 | + | Silent | SNP | C | C | A | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr1:235993607C>A | c.111G>T | c.(109-111)acG>acT | p.T37T |
LUSC | 1 | 235827887 | 235827887 | + | Silent | SNP | C | C | G | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr1:235827887C>G | c.11073G>C | c.(11071-11073)gtG>gtC | p.V3691V |
LUSC | 1 | 235840490 | 235840490 | + | Splice_Site | SNP | T | T | A | TCGA-18-3414-01A-01D-0983-08 | TCGA-18-3414-11A-01D-0983-08 | g.chr1:235840490T>A | | c.e50-2 | |
LUSC | 1 | 235860456 | 235860456 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2742-01A-01D-0983-08 | TCGA-66-2742-11A-01D-0983-08 | g.chr1:235860456C>A | c.10491G>T | c.(10489-10491)caG>caT | p.Q3497H |
LUSC | 1 | 235866082 | 235866082 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2778-01A-02D-1522-08 | TCGA-66-2778-11A-01D-1522-08 | g.chr1:235866082C>G | c.10339G>C | c.(10339-10341)Gag>Cag | p.E3447Q |
LUSC | 1 | 235892930 | 235892930 | + | Silent | SNP | T | T | C | TCGA-85-6560-01A-11D-1817-08 | TCGA-85-6560-10A-01D-1817-08 | g.chr1:235892930T>C | c.9072A>G | c.(9070-9072)gcA>gcG | p.A3024A |
LUSC | 1 | 235896901 | 235896901 | + | Missense_Mutation | SNP | C | C | A | TCGA-22-5482-01A-01D-1632-08 | TCGA-22-5482-11A-01D-1632-08 | g.chr1:235896901C>A | c.8703G>T | c.(8701-8703)gaG>gaT | p.E2901D |
LUSC | 1 | 235929511 | 235929511 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr1:235929511C>A | c.5989G>T | c.(5989-5991)Gca>Tca | p.A1997S |
LUSC | 1 | 235937219 | 235937219 | + | Missense_Mutation | SNP | C | C | G | TCGA-37-3783-01A-01D-1267-08 | TCGA-37-3783-10A-01D-1267-08 | g.chr1:235937219C>G | c.5707G>C | c.(5707-5709)Gac>Cac | p.D1903H |
LUSC | 1 | 235944340 | 235944340 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr1:235944340G>C | c.5039C>G | c.(5038-5040)tCa>tGa | p.S1680* |
LUSC | 1 | 235945292 | 235945292 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-33-4547-01A-01D-1267-08 | TCGA-33-4547-11A-01D-1267-08 | g.chr1:235945292G>T | c.4958C>A | c.(4957-4959)tCa>tAa | p.S1653* |
LUSC | 1 | 235955020 | 235955020 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr1:235955020C>A | c.4522G>T | c.(4522-4524)Gat>Tat | p.D1508Y |
LUSC | 1 | 235967923 | 235967923 | + | Missense_Mutation | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr1:235967923G>A | c.3436C>T | c.(3436-3438)Ctt>Ttt | p.L1146F |
LUSC | 1 | 235969140 | 235969140 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-66-2795-01A-02D-0983-08 | TCGA-66-2795-11A-01D-0983-08 | g.chr1:235969140G>T | c.3296C>A | c.(3295-3297)tCa>tAa | p.S1099* |
LUSC | 1 | 235969541 | 235969541 | + | Silent | SNP | A | A | T | TCGA-37-4135-01A-01D-1352-08 | TCGA-37-4135-10A-01D-1352-08 | g.chr1:235969541A>T | c.2895T>A | c.(2893-2895)tcT>tcA | p.S965S |
LUSC | 1 | 235972254 | 235972254 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-22-5489-01A-01D-1632-08 | TCGA-22-5489-11A-01D-1632-08 | g.chr1:235972254G>A | c.1864C>T | c.(1864-1866)Cag>Tag | p.Q622* |
LUSC | 1 | 235972330 | 235972330 | + | Silent | SNP | G | G | C | TCGA-22-5489-01A-01D-1632-08 | TCGA-22-5489-11A-01D-1632-08 | g.chr1:235972330G>C | c.1788C>G | c.(1786-1788)ctC>ctG | p.L596L |
LUSC | 1 | 235972415 | 235972415 | + | Missense_Mutation | SNP | C | C | A | TCGA-46-6025-01A-11D-1817-08 | TCGA-46-6025-10A-01D-1817-08 | g.chr1:235972415C>A | c.1703G>T | c.(1702-1704)aGc>aTc | p.S568I |
LUSC | 1 | 235973326 | 235973326 | + | Missense_Mutation | SNP | T | T | G | TCGA-33-4583-01A-01D-1441-08 | TCGA-33-4583-11A-01D-1441-08 | g.chr1:235973326T>G | c.792A>C | c.(790-792)ttA>ttC | p.L264F |
OV | 1 | 235840882 | 235840882 | + | Missense_Mutation | SNP | T | T | C | TCGA-23-2072-01A-01W-0722-08 | TCGA-23-2072-10A-01W-0722-08 | g.chr1:235840882T>C | c.10838A>G | c.(10837-10839)tAt>tGt | p.Y3613C |
OV | 1 | 235897870 | 235897870 | + | Silent | SNP | C | C | T | TCGA-13-1411-01A-01W-0494-09 | TCGA-13-1411-10A-01W-0495-09 | g.chr1:235897870C>T | c.8448G>A | c.(8446-8448)ctG>ctA | p.L2816L |
OV | 1 | 235929573 | 235929573 | + | Missense_Mutation | SNP | T | T | C | TCGA-61-1740-01A-01W-0639-09 | TCGA-61-1740-11A-01W-0639-09 | g.chr1:235929573T>C | c.5927A>G | c.(5926-5928)tAc>tGc | p.Y1976C |
OV | 1 | 235966296 | 235966296 | + | Missense_Mutation | SNP | C | C | A | TCGA-23-1123-01A-01W-0488-09 | TCGA-23-1123-10A-01W-0488-09 | g.chr1:235966296C>A | c.3624G>T | c.(3622-3624)caG>caT | p.Q1208H |
OV | 1 | 235969927 | 235969927 | + | Missense_Mutation | SNP | G | G | A | TCGA-13-0903-01A-01W-0421-09 | TCGA-13-0903-10A-01W-0421-09 | g.chr1:235969927G>A | c.2509C>T | c.(2509-2511)Cca>Tca | p.P837S |
OV | 1 | 235972337 | 235972337 | + | Missense_Mutation | SNP | G | G | T | TCGA-25-1313-01A-01W-0492-08 | TCGA-25-1313-10A-01W-0492-08 | g.chr1:235972337G>T | c.1781C>A | c.(1780-1782)cCt>cAt | p.P594H |
OV | 1 | 235993636 | 235993636 | + | Missense_Mutation | SNP | C | C | T | TCGA-25-1319-01A-01W-0492-08 | TCGA-25-1319-10A-01W-0492-08 | g.chr1:235993636C>T | c.82G>A | c.(82-84)Gag>Aag | p.E28K |
PAAD | 1 | 235826308 | 235826308 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235826308G>A | c.11338C>T | c.(11338-11340)Cgg>Tgg | p.R3780W |
PAAD | 1 | 235866228 | 235866228 | + | Missense_Mutation | SNP | C | C | A | TCGA-HZ-A77Q-01A-11D-A36O-08 | TCGA-HZ-A77Q-10A-01D-A367-08 | g.chr1:235866228C>A | c.10193G>T | c.(10192-10194)cGa>cTa | p.R3398L |
PAAD | 1 | 235909723 | 235909723 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235909723C>T | c.7885G>A | c.(7885-7887)Gag>Aag | p.E2629K |
PAAD | 1 | 235944227 | 235944227 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-IB-A7M4-01A-11D-A36O-08 | TCGA-IB-A7M4-10A-01D-A367-08 | g.chr1:235944227G>A | c.5152C>T | c.(5152-5154)Cga>Tga | p.R1718* |
PAAD | 1 | 235952092 | 235952092 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235952092C>T | c.4597G>A | c.(4597-4599)Gaa>Aaa | p.E1533K |
PAAD | 1 | 235955384 | 235955384 | + | Silent | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235955384A>G | c.4158T>C | c.(4156-4158)gaT>gaC | p.D1386D |
PAAD | 1 | 235964335 | 235964335 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235964335C>T | c.3775G>A | c.(3775-3777)Gaa>Aaa | p.E1259K |
PAAD | 1 | 235969949 | 235969949 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235969949C>A | c.2487G>T | c.(2485-2487)gaG>gaT | p.E829D |
PAAD | 1 | 235970023 | 235970023 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235970023C>T | c.2413G>A | c.(2413-2415)Gaa>Aaa | p.E805K |
PAAD | 1 | 235972089 | 235972089 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235972089T>C | c.2029A>G | c.(2029-2031)Atc>Gtc | p.I677V |
PAAD | 1 | 235973135 | 235973135 | + | Missense_Mutation | SNP | A | A | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr1:235973135A>C | c.983T>G | c.(982-984)tTt>tGt | p.F328C |
PCPG | 1 | 235929422 | 235929422 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-S7-A7WN-01A-12D-A35I-08 | TCGA-S7-A7WN-10A-01D-A35G-08 | g.chr1:235929422G>T | c.6078C>A | c.(6076-6078)taC>taA | p.Y2026* |
PCPG | 1 | 235940409 | 235940409 | + | Missense_Mutation | SNP | A | A | G | TCGA-RW-A680-01A-11D-A35D-08 | TCGA-RW-A680-10B-01D-A35B-08 | g.chr1:235940409A>G | c.5414T>C | c.(5413-5415)cTg>cCg | p.L1805P |
PCPG | 1 | 235969125 | 235969125 | + | Missense_Mutation | SNP | C | C | T | TCGA-RW-A67W-01A-11D-A35D-08 | TCGA-RW-A67W-10A-01D-A35B-08 | g.chr1:235969125C>T | c.3311G>A | c.(3310-3312)cGa>cAa | p.R1104Q |
PRAD | 1 | 235840808 | 235840808 | + | Missense_Mutation | SNP | C | C | T | TCGA-EJ-5498-01A-01D-1576-08 | TCGA-EJ-5498-10A-01D-1577-08 | g.chr1:235840808C>T | c.10912G>A | c.(10912-10914)Gga>Aga | p.G3638R |
PRAD | 1 | 235840908 | 235840908 | + | Missense_Mutation | SNP | T | T | C | TCGA-ZG-A9KY-01A-11D-A41K-08 | TCGA-ZG-A9KY-10A-01D-A41N-08 | g.chr1:235840908T>C | c.10812A>G | c.(10810-10812)atA>atG | p.I3604M |
PRAD | 1 | 235887435 | 235887435 | + | Missense_Mutation | SNP | C | C | T | TCGA-V1-A9ZG-01A-11D-A41K-08 | TCGA-V1-A9ZG-10A-01D-A41N-08 | g.chr1:235887435C>T | c.9208G>A | c.(9208-9210)Gaa>Aaa | p.E3070K |
PRAD | 1 | 235922371 | 235922371 | + | Missense_Mutation | SNP | C | C | T | TCGA-G9-A9S4-01A-11D-A41K-08 | TCGA-G9-A9S4-10A-01D-A41N-08 | g.chr1:235922371C>T | c.6782G>A | c.(6781-6783)cGt>cAt | p.R2261H |
PRAD | 1 | 235933474 | 235933482 | + | In_Frame_Del | DEL | AAGTCAGTA | AAGTCAGTA | - | TCGA-XA-A8JR-01A-11D-A364-08 | TCGA-XA-A8JR-10A-01D-A362-08 | g.chr1:235933474_235933482delAAGTCAGTA | c.5900_5908delTACTGACTT | c.(5899-5910)ctactgacttgt>cgt | p.1967_1970LLTC>R |
PRAD | 1 | 235944227 | 235944227 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-V1-A8WW-01A-11D-A377-08 | TCGA-V1-A8WW-10A-01D-A37A-08 | g.chr1:235944227G>A | c.5152C>T | c.(5152-5154)Cga>Tga | p.R1718* |
PRAD | 1 | 235944227 | 235944227 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr1:235944227G>A | c.5152C>T | c.(5152-5154)Cga>Tga | p.R1718* |
PRAD | 1 | 235950607 | 235950607 | + | Silent | SNP | A | A | G | TCGA-CH-5739-01A-11D-1576-08 | TCGA-CH-5739-10A-01D-1576-08 | g.chr1:235950607A>G | c.4755T>C | c.(4753-4755)aaT>aaC | p.N1585N |
PRAD | 1 | 235964219 | 235964220 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr1:235964219_235964220insA | c.3890_3891insT | c.(3889-3891)ttgfs | p.L1297fs |
PRAD | 1 | 235973754 | 235973754 | + | Missense_Mutation | SNP | A | A | T | TCGA-KK-A7AV-01A-11D-A32B-08 | TCGA-KK-A7AV-11A-11D-A329-08 | g.chr1:235973754A>T | c.364T>A | c.(364-366)Tta>Ata | p.L122I |
READ | 1 | 235826273 | 235826273 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235826273G>T | c.11373C>A | c.(11371-11373)ttC>ttA | p.F3791L |
READ | 1 | 235840882 | 235840882 | + | Missense_Mutation | SNP | T | T | C | TCGA-F5-6702-01A-11D-1826-10 | TCGA-F5-6702-10A-01D-1826-10 | g.chr1:235840882T>C | c.10838A>G | c.(10837-10839)tAt>tGt | p.Y3613C |
READ | 1 | 235840883 | 235840883 | + | Missense_Mutation | SNP | A | A | G | TCGA-DY-A1DG-01A-11D-A152-10 | TCGA-DY-A1DG-10A-01D-A152-10 | g.chr1:235840883A>G | c.10837T>C | c.(10837-10839)Tat>Cat | p.Y3613H |
READ | 1 | 235850291 | 235850291 | + | Silent | SNP | G | G | A | TCGA-DC-5337-01A-01D-1657-10 | TCGA-DC-5337-10A-01D-1657-10 | g.chr1:235850291G>A | c.10758C>T | c.(10756-10758)tgC>tgT | p.C3586C |
READ | 1 | 235920623 | 235920623 | + | Silent | SNP | G | G | A | TCGA-AG-3890-01A-01W-1073-09 | TCGA-AG-3890-10A-01W-1073-09 | g.chr1:235920623G>A | c.7017C>T | c.(7015-7017)ctC>ctT | p.L2339L |
READ | 1 | 235938335 | 235938335 | + | Missense_Mutation | SNP | T | T | C | TCGA-DY-A0XA-01A-11D-A152-10 | TCGA-DY-A0XA-10A-01D-A152-10 | g.chr1:235938335T>C | c.5512A>G | c.(5512-5514)Ata>Gta | p.I1838V |
READ | 1 | 235955020 | 235955020 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr1:235955020C>A | c.4522G>T | c.(4522-4524)Gat>Tat | p.D1508Y |
READ | 1 | 235969926 | 235969926 | + | Missense_Mutation | SNP | G | G | T | TCGA-F5-6464-01A-11D-1733-10 | TCGA-F5-6464-10A-01D-1733-10 | g.chr1:235969926G>T | c.2510C>A | c.(2509-2511)cCa>cAa | p.P837Q |
READ | 1 | 235972610 | 235972610 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235972610C>T | c.1508G>A | c.(1507-1509)cGa>cAa | p.R503Q |
READ | 1 | 235972904 | 235972904 | + | Missense_Mutation | SNP | A | A | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235972904A>G | c.1214T>C | c.(1213-1215)tTg>tCg | p.L405S |
READ | 1 | 235973133 | 235973133 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235973133G>A | c.985C>T | c.(985-987)Cga>Tga | p.R329* |
READ | 1 | 235973720 | 235973720 | + | Missense_Mutation | SNP | A | A | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr1:235973720A>G | c.398T>C | c.(397-399)gTt>gCt | p.V133A |
SARC | 1 | 235929492 | 235929492 | + | Missense_Mutation | SNP | G | G | A | TCGA-QQ-A5VD-01A-21D-A32I-09 | TCGA-QQ-A5VD-10A-01D-A32I-09 | g.chr1:235929492G>A | c.6008C>T | c.(6007-6009)cCt>cTt | p.P2003L |
SARC | 1 | 235929493 | 235929493 | + | Missense_Mutation | SNP | G | G | A | TCGA-QQ-A5VD-01A-21D-A32I-09 | TCGA-QQ-A5VD-10A-01D-A32I-09 | g.chr1:235929493G>A | c.6007C>T | c.(6007-6009)Cct>Tct | p.P2003S |
SARC | 1 | 235950617 | 235950617 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-IW-A3M4-01A-11D-A21Q-09 | TCGA-IW-A3M4-10B-01D-A21Q-09 | g.chr1:235950617G>T | c.4745C>A | c.(4744-4746)tCa>tAa | p.S1582* |
SARC | 1 | 235972736 | 235972736 | + | Missense_Mutation | SNP | A | A | G | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr1:235972736A>G | c.1382T>C | c.(1381-1383)gTt>gCt | p.V461A |
SKCM | 1 | 235827771 | 235827771 | + | Missense_Mutation | SNP | A | A | C | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr1:235827771A>C | c.11189T>G | c.(11188-11190)aTt>aGt | p.I3730S |
SKCM | 1 | 235840451 | 235840451 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr1:235840451G>A | c.10978C>T | c.(10978-10980)Cct>Tct | p.P3660S |
SKCM | 1 | 235860390 | 235860390 | + | Silent | SNP | C | C | T | TCGA-ER-A3PL-06A-11D-A23B-08 | TCGA-ER-A3PL-10A-01D-A23B-08 | g.chr1:235860390C>T | c.10557G>A | c.(10555-10557)aaG>aaA | p.K3519K |
SKCM | 1 | 235860522 | 235860522 | + | Silent | SNP | G | G | A | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr1:235860522G>A | c.10425C>T | c.(10423-10425)tcC>tcT | p.S3475S |
SKCM | 1 | 235866166 | 235866166 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr1:235866166G>A | c.10255C>T | c.(10255-10257)Cat>Tat | p.H3419Y |
SKCM | 1 | 235866167 | 235866167 | + | Silent | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr1:235866167G>A | c.10254C>T | c.(10252-10254)gcC>gcT | p.A3418A |
SKCM | 1 | 235866213 | 235866213 | + | Missense_Mutation | SNP | A | A | G | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr1:235866213A>G | c.10208T>C | c.(10207-10209)aTg>aCg | p.M3403T |
SKCM | 1 | 235884159 | 235884159 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr1:235884159T>A | c.9362A>T | c.(9361-9363)aAt>aTt | p.N3121I |
SKCM | 1 | 235887328 | 235887328 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr1:235887328C>T | c.9315G>A | c.(9313-9315)aaG>aaA | p.K3105K |
SKCM | 1 | 235891379 | 235891379 | + | Silent | SNP | A | A | G | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr1:235891379A>G | c.9159T>C | c.(9157-9159)agT>agC | p.S3053S |
SKCM | 1 | 235904728 | 235904728 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr1:235904728G>A | c.8352C>T | c.(8350-8352)tcC>tcT | p.S2784S |
SKCM | 1 | 235907411 | 235907411 | + | Silent | SNP | T | T | G | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr1:235907411T>G | c.8019A>C | c.(8017-8019)gtA>gtC | p.V2673V |
SKCM | 1 | 235915467 | 235915467 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr1:235915467G>A | c.7465C>T | c.(7465-7467)Ccc>Tcc | p.P2489S |
SKCM | 1 | 235922487 | 235922487 | + | Silent | SNP | G | G | A | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr1:235922487G>A | c.6666C>T | c.(6664-6666)tcC>tcT | p.S2222S |
SKCM | 1 | 235929509 | 235929509 | + | Silent | SNP | T | T | C | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr1:235929509T>C | c.5991A>G | c.(5989-5991)gcA>gcG | p.A1997A |
SKCM | 1 | 235950601 | 235950601 | + | Silent | SNP | G | G | A | TCGA-D3-A51J-06A-11D-A25O-08 | TCGA-D3-A51J-10A-01D-A25O-08 | g.chr1:235950601G>A | c.4761C>T | c.(4759-4761)ttC>ttT | p.F1587F |
SKCM | 1 | 235950643 | 235950643 | + | Silent | SNP | T | T | C | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr1:235950643T>C | c.4719A>G | c.(4717-4719)aaA>aaG | p.K1573K |
SKCM | 1 | 235955205 | 235955205 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3C8-06A-12D-A19A-08 | TCGA-D3-A3C8-10A-01D-A19A-08 | g.chr1:235955205C>T | c.4337G>A | c.(4336-4338)cGg>cAg | p.R1446Q |
SKCM | 1 | 235955367 | 235955367 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-FS-A1Z3-06A-11D-A197-08 | TCGA-FS-A1Z3-10A-01D-A199-08 | g.chr1:235955367G>T | c.4175C>A | c.(4174-4176)tCa>tAa | p.S1392* |
SKCM | 1 | 235956850 | 235956850 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JB-06A-11D-A21A-08 | TCGA-EE-A3JB-10A-01D-A21A-08 | g.chr1:235956850C>T | c.4069G>A | c.(4069-4071)Gag>Aag | p.E1357K |
SKCM | 1 | 235967804 | 235967804 | + | Splice_Site | SNP | C | C | T | TCGA-D3-A5GR-06A-11D-A27K-08 | TCGA-D3-A5GR-10A-01D-A27N-08 | g.chr1:235967804C>T | c.3555G>A | c.(3553-3555)aaG>aaA | p.K1185K |
SKCM | 1 | 235969062 | 235969062 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr1:235969062T>C | c.3374A>G | c.(3373-3375)gAa>gGa | p.E1125G |
SKCM | 1 | 235969138 | 235969138 | + | Missense_Mutation | SNP | G | G | A | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr1:235969138G>A | c.3298C>T | c.(3298-3300)Ctt>Ttt | p.L1100F |
SKCM | 1 | 235969221 | 235969221 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr1:235969221G>A | c.3215C>T | c.(3214-3216)tCc>tTc | p.S1072F |
SKCM | 1 | 235969576 | 235969576 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr1:235969576G>A | c.2860C>T | c.(2860-2862)Cct>Tct | p.P954S |
SKCM | 1 | 235969602 | 235969602 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZQ-06A-11D-A197-08 | TCGA-FS-A1ZQ-10A-01D-A199-08 | g.chr1:235969602G>A | c.2834C>T | c.(2833-2835)tCt>tTt | p.S945F |
SKCM | 1 | 235972340 | 235972340 | + | Missense_Mutation | SNP | A | A | G | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr1:235972340A>G | c.1778T>C | c.(1777-1779)aTt>aCt | p.I593T |
SKCM | 1 | 235972583 | 235972583 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr1:235972583T>C | c.1535A>G | c.(1534-1536)cAt>cGt | p.H512R |
SKCM | 1 | 235972605 | 235972605 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr1:235972605C>T | c.1513G>A | c.(1513-1515)Gaa>Aaa | p.E505K |
SKCM | 1 | 235972806 | 235972806 | + | Missense_Mutation | SNP | G | G | C | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr1:235972806G>C | c.1312C>G | c.(1312-1314)Cag>Gag | p.Q438E |
SKCM | 1 | 235973240 | 235973240 | + | Missense_Mutation | SNP | A | A | G | TCGA-ER-A19O-06A-11D-A197-08 | TCGA-ER-A19O-10A-01D-A199-08 | g.chr1:235973240A>G | c.878T>C | c.(877-879)cTa>cCa | p.L293P |
SKCM | 1 | 235973317 | 235973317 | + | Silent | SNP | T | T | C | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr1:235973317T>C | c.801A>G | c.(799-801)aaA>aaG | p.K267K |
SKCM | 1 | 235973358 | 235973358 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr1:235973358G>A | c.760C>T | c.(760-762)Cca>Tca | p.P254S |
SKCM | 1 | 235973516 | 235973516 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZM-06A-12D-A197-08 | TCGA-FS-A1ZM-10A-01D-A199-08 | g.chr1:235973516G>A | c.602C>T | c.(601-603)cCc>cTc | p.P201L |
SKCM | 1 | 235973692 | 235973692 | + | Missense_Mutation | SNP | T | T | G | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr1:235973692T>G | c.426A>C | c.(424-426)aaA>aaC | p.K142N |
SKCM | 1 | 235973733 | 235973733 | + | Silent | SNP | G | G | A | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr1:235973733G>A | c.385C>T | c.(385-387)Ctg>Ttg | p.L129L |
SKCM | 1 | 235973803 | 235973803 | + | Silent | SNP | G | G | A | TCGA-D3-A51J-06A-11D-A25O-08 | TCGA-D3-A51J-10A-01D-A25O-08 | g.chr1:235973803G>A | c.315C>T | c.(313-315)atC>atT | p.I105I |
SKCM | 1 | 235973814 | 235973814 | + | Missense_Mutation | SNP | C | C | G | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr1:235973814C>G | c.304G>C | c.(304-306)Gca>Cca | p.A102P |