| 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 | 8 | 103284937 | 103284937 | + | Silent | SNP | G | G | T | TCGA-OR-A5JA-01A-11D-A29I-10 | TCGA-OR-A5JA-10A-01D-A29L-10 | g.chr8:103284937G>T | c.6793C>A | c.(6793-6795)Cga>Aga | p.R2265R |
| ACC | 8 | 103297940 | 103297940 | + | Missense_Mutation | SNP | G | G | T | TCGA-OR-A5LB-01A-11D-A29I-10 | TCGA-OR-A5LB-10A-01D-A29L-10 | g.chr8:103297940G>T | c.5285C>A | c.(5284-5286)gCt>gAt | p.A1762D |
| ACC | 8 | 103297999 | 103297999 | + | Silent | SNP | C | C | T | TCGA-OR-A5LJ-01A-11D-A29I-10 | TCGA-OR-A5LJ-10A-01D-A29L-10 | g.chr8:103297999C>T | c.5226G>A | c.(5224-5226)gcG>gcA | p.A1742A |
| BLCA | 8 | 103266530 | 103266530 | + | Nonstop_Mutation | SNP | C | C | G | TCGA-FD-A5BX-01A-11D-A26M-08 | TCGA-FD-A5BX-10A-01D-A26K-08 | g.chr8:103266530C>G | c.8400G>C | c.(8398-8400)taG>taC | p.*2800Y |
| BLCA | 8 | 103266703 | 103266703 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A3WW-01A-22D-A23M-08 | TCGA-DK-A3WW-10A-01D-A23K-08 | g.chr8:103266703C>T | c.8227G>A | c.(8227-8229)Gaa>Aaa | p.E2743K |
| BLCA | 8 | 103277452 | 103277452 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A1AE-01A-11D-A13W-08 | TCGA-DK-A1AE-10A-01D-A13W-08 | g.chr8:103277452C>G | c.7477G>C | c.(7477-7479)Gat>Cat | p.D2493H |
| BLCA | 8 | 103277475 | 103277475 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr8:103277475C>T | c.7454G>A | c.(7453-7455)cGa>cAa | p.R2485Q |
| BLCA | 8 | 103277499 | 103277499 | + | Missense_Mutation | SNP | T | T | G | TCGA-2F-A9KR-01A-11D-A38G-08 | TCGA-2F-A9KR-10A-01D-A38J-08 | g.chr8:103277499T>G | c.7430A>C | c.(7429-7431)aAc>aCc | p.N2477T |
| BLCA | 8 | 103282413 | 103282414 | + | Splice_Site | DEL | TG | TG | - | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr8:103282413_103282414delTG | | c.e50-2 | |
| BLCA | 8 | 103284793 | 103284793 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9T8-01A-11D-A391-08 | TCGA-XF-A9T8-10A-01D-A394-08 | g.chr8:103284793C>G | c.6937G>C | c.(6937-6939)Gag>Cag | p.E2313Q |
| BLCA | 8 | 103284977 | 103284977 | + | Silent | SNP | G | G | A | TCGA-ZF-A9RC-01A-11D-A38G-08 | TCGA-ZF-A9RC-10A-01D-A38J-08 | g.chr8:103284977G>A | c.6753C>T | c.(6751-6753)ctC>ctT | p.L2251L |
| BLCA | 8 | 103284993 | 103284993 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A5BX-01A-11D-A26M-08 | TCGA-FD-A5BX-10A-01D-A26K-08 | g.chr8:103284993C>T | c.6737G>A | c.(6736-6738)cGg>cAg | p.R2246Q |
| BLCA | 8 | 103287765 | 103287765 | + | Missense_Mutation | SNP | C | C | G | TCGA-E7-A7DV-01A-11D-A339-08 | TCGA-E7-A7DV-10A-01D-A339-08 | g.chr8:103287765C>G | c.6713G>C | c.(6712-6714)aGa>aCa | p.R2238T |
| BLCA | 8 | 103287807 | 103287807 | + | Missense_Mutation | SNP | T | T | A | TCGA-DK-AA6U-01A-11D-A391-08 | TCGA-DK-AA6U-10A-01D-A394-08 | g.chr8:103287807T>A | c.6671A>T | c.(6670-6672)aAa>aTa | p.K2224I |
| BLCA | 8 | 103291056 | 103291056 | + | Missense_Mutation | SNP | C | C | G | TCGA-G2-AA3B-01A-11D-A391-08 | TCGA-G2-AA3B-10A-01D-A394-08 | g.chr8:103291056C>G | c.6286G>C | c.(6286-6288)Gag>Cag | p.E2096Q |
| BLCA | 8 | 103291080 | 103291080 | + | Missense_Mutation | SNP | C | C | A | TCGA-XF-A9SM-01A-11D-A42E-08 | TCGA-XF-A9SM-10A-01D-A42H-08 | g.chr8:103291080C>A | c.6262G>T | c.(6262-6264)Gtt>Ttt | p.V2088F |
| BLCA | 8 | 103291096 | 103291096 | + | Silent | SNP | C | C | T | TCGA-XF-AAN5-01A-11D-A42E-08 | TCGA-XF-AAN5-10A-01D-A42H-08 | g.chr8:103291096C>T | c.6246G>A | c.(6244-6246)ggG>ggA | p.G2082G |
| BLCA | 8 | 103291149 | 103291149 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A6TH-01A-11D-A32B-08 | TCGA-FD-A6TH-10A-01D-A329-08 | g.chr8:103291149C>T | c.6193G>A | c.(6193-6195)Gat>Aat | p.D2065N |
| BLCA | 8 | 103293664 | 103293664 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9RL-01A-11D-A38G-08 | TCGA-ZF-A9RL-10A-01D-A38J-08 | g.chr8:103293664G>C | c.5780C>G | c.(5779-5781)tCt>tGt | p.S1927C |
| BLCA | 8 | 103293699 | 103293699 | + | Silent | SNP | T | T | A | TCGA-ZF-A9RL-01A-11D-A38G-08 | TCGA-ZF-A9RL-10A-01D-A38J-08 | g.chr8:103293699T>A | c.5745A>T | c.(5743-5745)ggA>ggT | p.G1915G |
| BLCA | 8 | 103297768 | 103297768 | + | Missense_Mutation | SNP | C | C | G | TCGA-ZF-AA4X-01A-11D-A38G-08 | TCGA-ZF-AA4X-10A-01D-A38J-08 | g.chr8:103297768C>G | c.5457G>C | c.(5455-5457)ttG>ttC | p.L1819F |
| BLCA | 8 | 103298599 | 103298599 | + | Missense_Mutation | SNP | G | G | C | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr8:103298599G>C | c.5204C>G | c.(5203-5205)tCt>tGt | p.S1735C |
| BLCA | 8 | 103301731 | 103301731 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9SY-01A-21D-A42E-08 | TCGA-XF-A9SY-10A-01D-A42H-08 | g.chr8:103301731G>A | c.4663C>T | c.(4663-4665)Cgg>Tgg | p.R1555W |
| BLCA | 8 | 103301750 | 103301750 | + | Silent | SNP | G | G | T | TCGA-DK-A3IS-01A-21D-A21A-08 | TCGA-DK-A3IS-10A-01D-A21A-08 | g.chr8:103301750G>T | c.4644C>A | c.(4642-4644)atC>atA | p.I1548I |
| BLCA | 8 | 103305851 | 103305851 | + | Missense_Mutation | SNP | G | G | A | TCGA-GC-A3BM-01A-11D-A22Z-08 | TCGA-GC-A3BM-10A-01D-A22Z-08 | g.chr8:103305851G>A | c.4571C>T | c.(4570-4572)tCa>tTa | p.S1524L |
| BLCA | 8 | 103311099 | 103311099 | + | Silent | SNP | A | A | G | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr8:103311099A>G | c.3303T>C | c.(3301-3303)taT>taC | p.Y1101Y |
| BLCA | 8 | 103311734 | 103311734 | + | Missense_Mutation | SNP | G | G | C | TCGA-2F-A9KO-01A-11D-A38G-08 | TCGA-2F-A9KO-11A-12D-A38J-08 | g.chr8:103311734G>C | c.3148C>G | c.(3148-3150)Ctt>Gtt | p.L1050V |
| BLCA | 8 | 103323975 | 103323975 | + | Silent | SNP | G | G | A | TCGA-BT-A3PH-01A-11D-A21Z-08 | TCGA-BT-A3PH-10A-01D-A21Z-08 | g.chr8:103323975G>A | c.2406C>T | c.(2404-2406)ttC>ttT | p.F802F |
| BLCA | 8 | 103324050 | 103324050 | + | Silent | SNP | T | T | C | TCGA-YC-A9TC-01A-22D-A391-08 | TCGA-YC-A9TC-10A-01D-A394-08 | g.chr8:103324050T>C | c.2331A>G | c.(2329-2331)aaA>aaG | p.K777K |
| BLCA | 8 | 103324468 | 103324468 | + | Silent | SNP | G | G | C | TCGA-XF-AAMX-01A-11D-A42E-08 | TCGA-XF-AAMX-10A-01D-A42H-08 | g.chr8:103324468G>C | c.2157C>G | c.(2155-2157)gtC>gtG | p.V719V |
| BLCA | 8 | 103324700 | 103324700 | + | Missense_Mutation | SNP | T | T | C | TCGA-YF-AA3L-01A-11D-A38G-08 | TCGA-YF-AA3L-10A-01D-A38J-08 | g.chr8:103324700T>C | c.2021A>G | c.(2020-2022)gAt>gGt | p.D674G |
| BLCA | 8 | 103335546 | 103335546 | + | Missense_Mutation | SNP | C | C | T | TCGA-C4-A0F6-01A-11D-A10S-08 | TCGA-C4-A0F6-10A-01D-A10S-08 | g.chr8:103335546C>T | c.1777G>A | c.(1777-1779)Gaa>Aaa | p.E593K |
| BLCA | 8 | 103340046 | 103340046 | + | Missense_Mutation | SNP | G | G | T | TCGA-FD-A5BT-01A-11D-A26M-08 | TCGA-FD-A5BT-10A-01D-A26K-08 | g.chr8:103340046G>T | c.1405C>A | c.(1405-1407)Caa>Aaa | p.Q469K |
| BLCA | 8 | 103341574 | 103341574 | + | Silent | SNP | G | G | A | TCGA-DK-A3X1-01A-12D-A22Z-08 | TCGA-DK-A3X1-10A-01D-A22Z-08 | g.chr8:103341574G>A | c.1152C>T | c.(1150-1152)gtC>gtT | p.V384V |
| BLCA | 8 | 103354706 | 103354706 | + | Missense_Mutation | SNP | C | C | G | TCGA-H4-A2HQ-01A-11D-A17V-08 | TCGA-H4-A2HQ-10A-01D-A17V-08 | g.chr8:103354706C>G | c.1093G>C | c.(1093-1095)Gat>Cat | p.D365H |
| BLCA | 8 | 103357737 | 103357737 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SM-01A-11D-A22Z-08 | TCGA-FD-A3SM-10A-01D-A22Z-08 | g.chr8:103357737G>A | c.773C>T | c.(772-774)tCt>tTt | p.S258F |
| BLCA | 8 | 103357737 | 103357737 | + | Missense_Mutation | SNP | G | G | C | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr8:103357737G>C | c.773C>G | c.(772-774)tCt>tGt | p.S258C |
| BLCA | 8 | 103357753 | 103357753 | + | Missense_Mutation | SNP | C | C | G | TCGA-E7-A3X6-01A-12D-A22Z-08 | TCGA-E7-A3X6-10A-01D-A22Z-08 | g.chr8:103357753C>G | c.757G>C | c.(757-759)Gat>Cat | p.D253H |
| BLCA | 8 | 103358508 | 103358508 | + | Missense_Mutation | SNP | C | C | T | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chr8:103358508C>T | c.692G>A | c.(691-693)gGa>gAa | p.G231E |
| BLCA | 8 | 103358578 | 103358578 | + | Missense_Mutation | SNP | C | C | T | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chr8:103358578C>T | c.622G>A | c.(622-624)Gaa>Aaa | p.E208K |
| BLCA | 8 | 103359184 | 103359184 | + | Missense_Mutation | SNP | G | G | C | TCGA-4Z-AA87-01A-11D-A391-08 | TCGA-4Z-AA87-10A-01D-A394-08 | g.chr8:103359184G>C | c.523C>G | c.(523-525)Cag>Gag | p.Q175E |
| BLCA | 8 | 103372333 | 103372333 | + | Missense_Mutation | SNP | C | C | G | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr8:103372333C>G | c.352G>C | c.(352-354)Gag>Cag | p.E118Q |
| BLCA | 8 | 103373849 | 103373849 | + | Missense_Mutation | SNP | C | C | T | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chr8:103373849C>T | c.68G>A | c.(67-69)cGa>cAa | p.R23Q |
| BLCA | 8 | 103373850 | 103373850 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A3B5-01A-11D-A20D-08 | TCGA-FD-A3B5-10A-01D-A20D-08 | g.chr8:103373850G>C | c.67C>G | c.(67-69)Cga>Gga | p.R23G |
| BRCA | 8 | 103271312 | 103271312 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AQ-A04L-01B-21D-A10M-09 | TCGA-AQ-A04L-10A-01D-A12J-09 | g.chr8:103271312C>A | c.8002G>T | c.(8002-8004)Gaa>Taa | p.E2668* |
| BRCA | 8 | 103274157 | 103274157 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A0HK-01A-11W-A071-09 | TCGA-BH-A0HK-10A-01W-A071-09 | g.chr8:103274157C>T | c.7828G>A | c.(7828-7830)Gaa>Aaa | p.E2610K |
| BRCA | 8 | 103282400 | 103282400 | + | Missense_Mutation | SNP | C | C | A | TCGA-E2-A1LH-01A-11D-A14G-09 | TCGA-E2-A1LH-11A-22D-A14G-09 | g.chr8:103282400C>A | c.7097G>T | c.(7096-7098)aGa>aTa | p.R2366I |
| BRCA | 8 | 103284779 | 103284779 | + | Missense_Mutation | SNP | A | A | T | TCGA-B6-A0I1-01A-11D-A21Q-09 | TCGA-B6-A0I1-10A-01D-A21Q-09 | g.chr8:103284779A>T | c.6951T>A | c.(6949-6951)aaT>aaA | p.N2317K |
| BRCA | 8 | 103284880 | 103284880 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A2L8-01A-11D-A18P-09 | TCGA-BH-A2L8-10A-01D-A18P-09 | g.chr8:103284880C>T | c.6850G>A | c.(6850-6852)Gag>Aag | p.E2284K |
| BRCA | 8 | 103284901 | 103284901 | + | Missense_Mutation | SNP | C | C | T | TCGA-E2-A14P-01A-31D-A12B-09 | TCGA-E2-A14P-10A-01D-A12B-09 | g.chr8:103284901C>T | c.6829G>A | c.(6829-6831)Gta>Ata | p.V2277I |
| BRCA | 8 | 103284937 | 103284937 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr8:103284937G>A | c.6793C>T | c.(6793-6795)Cga>Tga | p.R2265* |
| BRCA | 8 | 103287948 | 103287948 | + | Silent | SNP | T | T | A | TCGA-A8-A09I-01A-22W-A050-09 | TCGA-A8-A09I-10A-01W-A055-09 | g.chr8:103287948T>A | c.6618A>T | c.(6616-6618)gcA>gcT | p.A2206A |
| BRCA | 8 | 103291157 | 103291157 | + | Missense_Mutation | SNP | C | C | T | TCGA-AO-A0J9-01A-11W-A050-09 | TCGA-AO-A0J9-10A-01W-A055-09 | g.chr8:103291157C>T | c.6185G>A | c.(6184-6186)aGa>aAa | p.R2062K |
| BRCA | 8 | 103291367 | 103291367 | + | Missense_Mutation | SNP | C | C | T | TCGA-A2-A3XZ-01A-42D-A23C-09 | TCGA-A2-A3XZ-10A-01D-A23C-09 | g.chr8:103291367C>T | c.6071G>A | c.(6070-6072)cGa>cAa | p.R2024Q |
| BRCA | 8 | 103297407 | 103297407 | + | Missense_Mutation | SNP | C | C | T | TCGA-C8-A27B-01A-11D-A167-09 | TCGA-C8-A27B-10A-01D-A167-09 | g.chr8:103297407C>T | c.5644G>A | c.(5644-5646)Gag>Aag | p.E1882K |
| BRCA | 8 | 103297830 | 103297830 | + | Missense_Mutation | SNP | T | T | C | TCGA-E2-A1II-01A-11D-A142-09 | TCGA-E2-A1II-10A-01D-A142-09 | g.chr8:103297830T>C | c.5395A>G | c.(5395-5397)Atg>Gtg | p.M1799V |
| BRCA | 8 | 103298762 | 103298762 | + | Missense_Mutation | SNP | T | T | A | TCGA-AN-A0FT-01A-11W-A050-09 | TCGA-AN-A0FT-10A-01W-A055-09 | g.chr8:103298762T>A | c.5041A>T | c.(5041-5043)Agt>Tgt | p.S1681C |
| BRCA | 8 | 103298799 | 103298799 | + | Silent | SNP | C | C | A | TCGA-BH-A0BD-01A-11W-A050-09 | TCGA-BH-A0BD-10A-01W-A055-09 | g.chr8:103298799C>A | c.5004G>T | c.(5002-5004)tcG>tcT | p.S1668S |
| BRCA | 8 | 103299695 | 103299695 | + | Silent | SNP | G | G | A | TCGA-A2-A0T0-01A-22D-A099-09 | TCGA-A2-A0T0-10A-01D-A099-09 | g.chr8:103299695G>A | c.4923C>T | c.(4921-4923)agC>agT | p.S1641S |
| BRCA | 8 | 103307462 | 103307462 | + | Missense_Mutation | SNP | A | A | T | TCGA-C8-A26Y-01A-11D-A16D-09 | TCGA-C8-A26Y-10A-01D-A16D-09 | g.chr8:103307462A>T | c.4028T>A | c.(4027-4029)aTt>aAt | p.I1343N |
| BRCA | 8 | 103307710 | 103307710 | + | Missense_Mutation | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr8:103307710A>C | c.3863T>G | c.(3862-3864)gTg>gGg | p.V1288G |
| BRCA | 8 | 103309809 | 103309809 | + | Silent | SNP | C | C | T | TCGA-A8-A09D-01A-11W-A019-09 | TCGA-A8-A09D-10A-01W-A021-09 | g.chr8:103309809C>T | c.3450G>A | c.(3448-3450)gaG>gaA | p.E1150E |
| BRCA | 8 | 103323670 | 103323670 | + | Missense_Mutation | SNP | C | C | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr8:103323670C>A | c.2473G>T | c.(2473-2475)Gat>Tat | p.D825Y |
| BRCA | 8 | 103324594 | 103324594 | + | Silent | SNP | C | C | T | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chr8:103324594C>T | c.2127G>A | c.(2125-2127)agG>agA | p.R709R |
| BRCA | 8 | 103324645 | 103324645 | + | Silent | SNP | C | C | T | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chr8:103324645C>T | c.2076G>A | c.(2074-2076)caG>caA | p.Q692Q |
| BRCA | 8 | 103335715 | 103335715 | + | Missense_Mutation | SNP | C | C | A | TCGA-A7-A0D9-01A-31W-A071-09 | TCGA-A7-A0D9-11A-53W-A100-09 | g.chr8:103335715C>A | c.1608G>T | c.(1606-1608)ttG>ttT | p.L536F |
| CESC | 8 | 103269876 | 103269876 | + | Missense_Mutation | SNP | G | G | T | TCGA-EK-A2RB-01A-11D-A18J-09 | TCGA-EK-A2RB-10A-01D-A18J-09 | g.chr8:103269876G>T | c.8171C>A | c.(8170-8172)aCa>aAa | p.T2724K |
| CESC | 8 | 103297358 | 103297358 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr8:103297358C>T | c.5693G>A | c.(5692-5694)aGa>aAa | p.R1898K |
| CESC | 8 | 103299757 | 103299757 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1MK-01A-11D-A14W-08 | TCGA-C5-A1MK-10A-01D-A14W-08 | g.chr8:103299757C>T | c.4861G>A | c.(4861-4863)Gaa>Aaa | p.E1621K |
| CESC | 8 | 103335715 | 103335715 | + | Missense_Mutation | SNP | C | C | G | TCGA-DS-A5RQ-01A-11D-A28B-09 | TCGA-DS-A5RQ-10A-01D-A28E-09 | g.chr8:103335715C>G | c.1608G>C | c.(1606-1608)ttG>ttC | p.L536F |
| CESC | 8 | 103338802 | 103338802 | + | Missense_Mutation | SNP | G | G | A | TCGA-IR-A3LH-01A-21D-A20U-09 | TCGA-IR-A3LH-10A-01D-A20U-09 | g.chr8:103338802G>A | c.1571C>T | c.(1570-1572)tCa>tTa | p.S524L |
| CESC | 8 | 103341421 | 103341421 | + | Missense_Mutation | SNP | G | G | A | TCGA-IR-A3LK-01A-12D-A20U-09 | TCGA-IR-A3LK-10A-01D-A20U-09 | g.chr8:103341421G>A | c.1223C>T | c.(1222-1224)tCa>tTa | p.S408L |
| CESC | 8 | 103358560 | 103358560 | + | Missense_Mutation | SNP | G | G | C | TCGA-EK-A2RJ-01A-11D-A18J-09 | TCGA-EK-A2RJ-10A-01D-A18J-09 | g.chr8:103358560G>C | c.640C>G | c.(640-642)Ctt>Gtt | p.L214V |
| CESC | 8 | 103358595 | 103358595 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr8:103358595C>T | c.605G>A | c.(604-606)aGa>aAa | p.R202K |
| CESC | 8 | 103359135 | 103359135 | + | Missense_Mutation | SNP | G | G | A | TCGA-EA-A3Y4-01A-51D-A243-09 | TCGA-EA-A3Y4-10A-01D-A243-09 | g.chr8:103359135G>A | c.572C>T | c.(571-573)tCa>tTa | p.S191L |
| CHOL | 8 | 103299709 | 103299709 | + | Missense_Mutation | SNP | T | T | C | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr8:103299709T>C | c.4909A>G | c.(4909-4911)Agt>Ggt | p.S1637G |
| CHOL | 8 | 103299714 | 103299714 | + | Missense_Mutation | SNP | T | T | G | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr8:103299714T>G | c.4904A>C | c.(4903-4905)aAt>aCt | p.N1635T |
| COAD | 8 | 103266583 | 103266583 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr8:103266583G>T | c.8347C>A | c.(8347-8349)Ctc>Atc | p.L2783I |
| COAD | 8 | 103271264 | 103271264 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr8:103271264C>T | c.8050G>A | c.(8050-8052)Gaa>Aaa | p.E2684K |
| COAD | 8 | 103274272 | 103274272 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr8:103274272delA | c.7713delT | c.(7711-7713)tttfs | p.F2571fs |
| COAD | 8 | 103277450 | 103277450 | + | Silent | SNP | A | A | G | TCGA-DM-A0XF-01A-11D-A152-10 | TCGA-DM-A0XF-10A-01D-A152-10 | g.chr8:103277450A>G | c.7479T>C | c.(7477-7479)gaT>gaC | p.D2493D |
| COAD | 8 | 103277450 | 103277450 | + | Silent | SNP | A | A | G | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr8:103277450A>G | c.7479T>C | c.(7477-7479)gaT>gaC | p.D2493D |
| COAD | 8 | 103277451 | 103277451 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr8:103277451T>C | c.7478A>G | c.(7477-7479)gAt>gGt | p.D2493G |
| COAD | 8 | 103277451 | 103277451 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr8:103277451T>C | c.7478A>G | c.(7477-7479)gAt>gGt | p.D2493G |
| COAD | 8 | 103277452 | 103277452 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6315-01A-11D-1719-10 | TCGA-G4-6315-10A-01D-1720-10 | g.chr8:103277452C>A | c.7477G>T | c.(7477-7479)Gat>Tat | p.D2493Y |
| COAD | 8 | 103277497 | 103277497 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DM-A0XF-01A-11D-A152-10 | TCGA-DM-A0XF-10A-01D-A152-10 | g.chr8:103277497G>A | c.7432C>T | c.(7432-7434)Cga>Tga | p.R2478* |
| COAD | 8 | 103287998 | 103287998 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr8:103287998G>A | c.6568C>T | c.(6568-6570)Cgc>Tgc | p.R2190C |
| COAD | 8 | 103291141 | 103291141 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr8:103291141delA | c.6201delT | c.(6199-6201)tttfs | p.F2067fs |
| COAD | 8 | 103291333 | 103291333 | + | Missense_Mutation | SNP | T | T | C | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr8:103291333T>C | c.6105A>G | c.(6103-6105)atA>atG | p.I2035M |
| COAD | 8 | 103291371 | 103291371 | + | Missense_Mutation | SNP | A | A | G | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr8:103291371A>G | c.6067T>C | c.(6067-6069)Ttc>Ctc | p.F2023L |
| COAD | 8 | 103292684 | 103292684 | + | Missense_Mutation | SNP | A | A | G | TCGA-DM-A1D7-01A-11D-A152-10 | TCGA-DM-A1D7-10A-01D-A152-10 | g.chr8:103292684A>G | c.5939T>C | c.(5938-5940)cTc>cCc | p.L1980P |
| COAD | 8 | 103292684 | 103292684 | + | Missense_Mutation | SNP | A | A | G | TCGA-DM-A28H-01A-11D-A16V-10 | TCGA-DM-A28H-10A-01D-A16V-10 | g.chr8:103292684A>G | c.5939T>C | c.(5938-5940)cTc>cCc | p.L1980P |
| COAD | 8 | 103292689 | 103292689 | + | Silent | SNP | T | T | A | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr8:103292689T>A | c.5934A>T | c.(5932-5934)cgA>cgT | p.R1978R |
| COAD | 8 | 103292689 | 103292689 | + | Silent | SNP | T | T | C | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chr8:103292689T>C | c.5934A>G | c.(5932-5934)cgA>cgG | p.R1978R |
| COAD | 8 | 103292689 | 103292689 | + | Silent | SNP | T | T | C | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr8:103292689T>C | c.5934A>G | c.(5932-5934)cgA>cgG | p.R1978R |
| COAD | 8 | 103292691 | 103292691 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr8:103292691G>A | c.5932C>T | c.(5932-5934)Cga>Tga | p.R1978* |
| COAD | 8 | 103292692 | 103292692 | + | Silent | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr8:103292692C>T | c.5931G>A | c.(5929-5931)acG>acA | p.T1977T |
| COAD | 8 | 103297374 | 103297374 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr8:103297374G>A | c.5677C>T | c.(5677-5679)Cga>Tga | p.R1893* |
| COAD | 8 | 103300407 | 103300407 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-A01F-01A-01W-A005-10 | TCGA-AA-A01F-10A-01W-A005-10 | g.chr8:103300407G>A | c.4801C>T | c.(4801-4803)Caa>Taa | p.Q1601* |
| COAD | 8 | 103307431 | 103307431 | + | Splice_Site | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr8:103307431C>T | | c.e31+1 | |
| COAD | 8 | 103307432 | 103307432 | + | Splice_Site | SNP | G | G | A | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr8:103307432G>A | c.4058C>T | c.(4057-4059)cCt>cTt | p.P1353L |
| COAD | 8 | 103307499 | 103307499 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:103307499G>A | c.3991C>T | c.(3991-3993)Cgt>Tgt | p.R1331C |
| COAD | 8 | 103311189 | 103311189 | + | Silent | SNP | T | T | C | TCGA-AA-A01Q-01A-01W-A005-10 | TCGA-AA-A01Q-10A-01W-A005-10 | g.chr8:103311189T>C | c.3213A>G | c.(3211-3213)acA>acG | p.T1071T |
| COAD | 8 | 103316322 | 103316322 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6679-01A-11D-1835-10 | TCGA-CM-6679-10A-01D-1835-10 | g.chr8:103316322A>G | c.2903T>C | c.(2902-2904)gTt>gCt | p.V968A |
| COAD | 8 | 103323533 | 103323533 | + | Silent | SNP | A | A | G | TCGA-G4-6303-01A-11D-1771-10 | TCGA-G4-6303-10A-01D-1771-10 | g.chr8:103323533A>G | c.2610T>C | c.(2608-2610)gcT>gcC | p.A870A |
| COAD | 8 | 103323535 | 103323535 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A28G-01A-11D-A16V-10 | TCGA-DM-A28G-10A-01D-A16V-10 | g.chr8:103323535C>A | c.2608G>T | c.(2608-2610)Gct>Tct | p.A870S |
| COAD | 8 | 103323535 | 103323535 | + | Missense_Mutation | SNP | C | C | T | TCGA-DM-A0X9-01A-11D-A152-10 | TCGA-DM-A0X9-10A-01D-A152-10 | g.chr8:103323535C>T | c.2608G>A | c.(2608-2610)Gct>Act | p.A870T |
| COAD | 8 | 103324084 | 103324084 | + | Missense_Mutation | SNP | A | A | G | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr8:103324084A>G | c.2297T>C | c.(2296-2298)gTa>gCa | p.V766A |
| COAD | 8 | 103327018 | 103327018 | + | Silent | SNP | C | C | T | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr8:103327018C>T | c.1848G>A | c.(1846-1848)acG>acA | p.T616T |
| COAD | 8 | 103338852 | 103338852 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:103338852C>A | c.1521G>T | c.(1519-1521)gaG>gaT | p.E507D |
| COAD | 8 | 103354749 | 103354749 | + | Silent | SNP | A | A | G | TCGA-CA-6715-01A-21D-1835-10 | TCGA-CA-6715-10A-01D-1835-10 | g.chr8:103354749A>G | c.1050T>C | c.(1048-1050)gtT>gtC | p.V350V |
| COAD | 8 | 103354749 | 103354749 | + | Silent | SNP | A | A | G | TCGA-G4-6299-01A-11D-1771-10 | TCGA-G4-6299-10A-01D-1771-10 | g.chr8:103354749A>G | c.1050T>C | c.(1048-1050)gtT>gtC | p.V350V |
| COAD | 8 | 103354750 | 103354750 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6323-01A-11D-1719-10 | TCGA-G4-6323-10A-01D-1720-10 | g.chr8:103354750A>G | c.1049T>C | c.(1048-1050)gTt>gCt | p.V350A |
| COAD | 8 | 103354846 | 103354846 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr8:103354846C>T | c.953G>A | c.(952-954)cGt>cAt | p.R318H |
| COAD | 8 | 103354869 | 103354869 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr8:103354869T>A | c.930A>T | c.(928-930)gaA>gaT | p.E310D |
| COAD | 8 | 103358496 | 103358497 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr8:103358496_103358497insC | c.703_704insG | c.(703-705)gatfs | p.D235fs |
| COAD | 8 | 103359252 | 103359252 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-5538-01A-01D-1650-10 | TCGA-D5-5538-10A-02D-1650-10 | g.chr8:103359252C>T | c.455G>A | c.(454-456)cGa>cAa | p.R152Q |
| COAD | 8 | 103359262 | 103359262 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr8:103359262C>T | c.445G>A | c.(445-447)Gct>Act | p.A149T |
| COAD | 8 | 103372360 | 103372360 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr8:103372360C>T | c.325G>A | c.(325-327)Gac>Aac | p.D109N |
| COAD | 8 | 103372382 | 103372382 | + | Silent | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr8:103372382C>T | c.303G>A | c.(301-303)acG>acA | p.T101T |
| COADREAD | 8 | 103266583 | 103266583 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr8:103266583G>T | c.8347C>A | c.(8347-8349)Ctc>Atc | p.L2783I |
| COADREAD | 8 | 103266662 | 103266662 | + | Silent | SNP | T | T | G | TCGA-CL-5917-01A-11D-1657-10 | TCGA-CL-5917-10A-01D-1657-10 | g.chr8:103266662T>G | c.8268A>C | c.(8266-8268)ccA>ccC | p.P2756P |
| COADREAD | 8 | 103269876 | 103269876 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3575-01A-01W-0831-10 | TCGA-AG-3575-10A-01W-0831-10 | g.chr8:103269876G>A | c.8171C>T | c.(8170-8172)aCa>aTa | p.T2724I |
| COADREAD | 8 | 103271264 | 103271264 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr8:103271264C>T | c.8050G>A | c.(8050-8052)Gaa>Aaa | p.E2684K |
| COADREAD | 8 | 103274272 | 103274272 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr8:103274272delA | c.7713delT | c.(7711-7713)tttfs | p.F2571fs |
| COADREAD | 8 | 103277450 | 103277450 | + | Silent | SNP | A | A | G | TCGA-DM-A0XF-01A-11D-A152-10 | TCGA-DM-A0XF-10A-01D-A152-10 | g.chr8:103277450A>G | c.7479T>C | c.(7477-7479)gaT>gaC | p.D2493D |
| COADREAD | 8 | 103277450 | 103277450 | + | Silent | SNP | A | A | G | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr8:103277450A>G | c.7479T>C | c.(7477-7479)gaT>gaC | p.D2493D |
| COADREAD | 8 | 103277451 | 103277451 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr8:103277451T>C | c.7478A>G | c.(7477-7479)gAt>gGt | p.D2493G |
| COADREAD | 8 | 103277451 | 103277451 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr8:103277451T>C | c.7478A>G | c.(7477-7479)gAt>gGt | p.D2493G |
| COADREAD | 8 | 103277452 | 103277452 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6315-01A-11D-1719-10 | TCGA-G4-6315-10A-01D-1720-10 | g.chr8:103277452C>A | c.7477G>T | c.(7477-7479)Gat>Tat | p.D2493Y |
| COADREAD | 8 | 103277497 | 103277497 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DM-A0XF-01A-11D-A152-10 | TCGA-DM-A0XF-10A-01D-A152-10 | g.chr8:103277497G>A | c.7432C>T | c.(7432-7434)Cga>Tga | p.R2478* |
| COADREAD | 8 | 103284867 | 103284867 | + | Missense_Mutation | SNP | C | C | T | TCGA-F5-6465-01A-11D-1733-10 | TCGA-F5-6465-10A-01D-1733-10 | g.chr8:103284867C>T | c.6863G>A | c.(6862-6864)gGc>gAc | p.G2288D |
| COADREAD | 8 | 103287998 | 103287998 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr8:103287998G>A | c.6568C>T | c.(6568-6570)Cgc>Tgc | p.R2190C |
| COADREAD | 8 | 103291141 | 103291141 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr8:103291141delA | c.6201delT | c.(6199-6201)tttfs | p.F2067fs |
| COADREAD | 8 | 103291333 | 103291333 | + | Missense_Mutation | SNP | T | T | C | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr8:103291333T>C | c.6105A>G | c.(6103-6105)atA>atG | p.I2035M |
| COADREAD | 8 | 103291365 | 103291365 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr8:103291365G>A | c.6073C>T | c.(6073-6075)Cgt>Tgt | p.R2025C |
| COADREAD | 8 | 103291371 | 103291371 | + | Missense_Mutation | SNP | A | A | G | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr8:103291371A>G | c.6067T>C | c.(6067-6069)Ttc>Ctc | p.F2023L |
| COADREAD | 8 | 103292684 | 103292684 | + | Missense_Mutation | SNP | A | A | G | TCGA-DM-A1D7-01A-11D-A152-10 | TCGA-DM-A1D7-10A-01D-A152-10 | g.chr8:103292684A>G | c.5939T>C | c.(5938-5940)cTc>cCc | p.L1980P |
| COADREAD | 8 | 103292684 | 103292684 | + | Missense_Mutation | SNP | A | A | G | TCGA-DM-A28H-01A-11D-A16V-10 | TCGA-DM-A28H-10A-01D-A16V-10 | g.chr8:103292684A>G | c.5939T>C | c.(5938-5940)cTc>cCc | p.L1980P |
| COADREAD | 8 | 103292689 | 103292689 | + | Silent | SNP | T | T | A | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr8:103292689T>A | c.5934A>T | c.(5932-5934)cgA>cgT | p.R1978R |
| COADREAD | 8 | 103292689 | 103292689 | + | Silent | SNP | T | T | C | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chr8:103292689T>C | c.5934A>G | c.(5932-5934)cgA>cgG | p.R1978R |
| COADREAD | 8 | 103292689 | 103292689 | + | Silent | SNP | T | T | C | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr8:103292689T>C | c.5934A>G | c.(5932-5934)cgA>cgG | p.R1978R |
| COADREAD | 8 | 103292691 | 103292691 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr8:103292691G>A | c.5932C>T | c.(5932-5934)Cga>Tga | p.R1978* |
| COADREAD | 8 | 103292692 | 103292692 | + | Silent | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr8:103292692C>T | c.5931G>A | c.(5929-5931)acG>acA | p.T1977T |
| COADREAD | 8 | 103297374 | 103297374 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr8:103297374G>A | c.5677C>T | c.(5677-5679)Cga>Tga | p.R1893* |
| COADREAD | 8 | 103299706 | 103299706 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3999-01A-01W-1073-09 | TCGA-AG-3999-10A-01W-1073-09 | g.chr8:103299706C>T | c.4912G>A | c.(4912-4914)Ggg>Agg | p.G1638R |
| COADREAD | 8 | 103300407 | 103300407 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-A01F-01A-01W-A005-10 | TCGA-AA-A01F-10A-01W-A005-10 | g.chr8:103300407G>A | c.4801C>T | c.(4801-4803)Caa>Taa | p.Q1601* |
| COADREAD | 8 | 103307431 | 103307431 | + | Splice_Site | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr8:103307431C>T | | c.e31+1 | |
| COADREAD | 8 | 103307432 | 103307432 | + | Splice_Site | SNP | G | G | A | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr8:103307432G>A | c.4058C>T | c.(4057-4059)cCt>cTt | p.P1353L |
| COADREAD | 8 | 103307499 | 103307499 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:103307499G>A | c.3991C>T | c.(3991-3993)Cgt>Tgt | p.R1331C |
| COADREAD | 8 | 103311189 | 103311189 | + | Silent | SNP | T | T | C | TCGA-AA-A01Q-01A-01W-A005-10 | TCGA-AA-A01Q-10A-01W-A005-10 | g.chr8:103311189T>C | c.3213A>G | c.(3211-3213)acA>acG | p.T1071T |
| COADREAD | 8 | 103316322 | 103316322 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6679-01A-11D-1835-10 | TCGA-CM-6679-10A-01D-1835-10 | g.chr8:103316322A>G | c.2903T>C | c.(2902-2904)gTt>gCt | p.V968A |
| COADREAD | 8 | 103317375 | 103317375 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3584-01A-01W-0831-10 | TCGA-AG-3584-10A-01W-0831-10 | g.chr8:103317375A>C | c.2765T>G | c.(2764-2766)aTt>aGt | p.I922S |
| COADREAD | 8 | 103317461 | 103317461 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:103317461C>A | c.2679G>T | c.(2677-2679)atG>atT | p.M893I |
| COADREAD | 8 | 103323533 | 103323533 | + | Silent | SNP | A | A | G | TCGA-G4-6303-01A-11D-1771-10 | TCGA-G4-6303-10A-01D-1771-10 | g.chr8:103323533A>G | c.2610T>C | c.(2608-2610)gcT>gcC | p.A870A |
| COADREAD | 8 | 103323535 | 103323535 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A28G-01A-11D-A16V-10 | TCGA-DM-A28G-10A-01D-A16V-10 | g.chr8:103323535C>A | c.2608G>T | c.(2608-2610)Gct>Tct | p.A870S |
| COADREAD | 8 | 103323535 | 103323535 | + | Missense_Mutation | SNP | C | C | T | TCGA-DM-A0X9-01A-11D-A152-10 | TCGA-DM-A0X9-10A-01D-A152-10 | g.chr8:103323535C>T | c.2608G>A | c.(2608-2610)Gct>Act | p.A870T |
| COADREAD | 8 | 103324084 | 103324084 | + | Missense_Mutation | SNP | A | A | G | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr8:103324084A>G | c.2297T>C | c.(2296-2298)gTa>gCa | p.V766A |
| COADREAD | 8 | 103327018 | 103327018 | + | Silent | SNP | C | C | T | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr8:103327018C>T | c.1848G>A | c.(1846-1848)acG>acA | p.T616T |
| COADREAD | 8 | 103338852 | 103338852 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:103338852C>A | c.1521G>T | c.(1519-1521)gaG>gaT | p.E507D |
| COADREAD | 8 | 103341610 | 103341610 | + | Silent | SNP | G | G | A | TCGA-AG-3612-01A-01W-0833-10 | TCGA-AG-3612-10A-01W-0833-10 | g.chr8:103341610G>A | c.1116C>T | c.(1114-1116)atC>atT | p.I372I |
| COADREAD | 8 | 103354749 | 103354749 | + | Silent | SNP | A | A | G | TCGA-CA-6715-01A-21D-1835-10 | TCGA-CA-6715-10A-01D-1835-10 | g.chr8:103354749A>G | c.1050T>C | c.(1048-1050)gtT>gtC | p.V350V |
| COADREAD | 8 | 103354749 | 103354749 | + | Silent | SNP | A | A | G | TCGA-G4-6299-01A-11D-1771-10 | TCGA-G4-6299-10A-01D-1771-10 | g.chr8:103354749A>G | c.1050T>C | c.(1048-1050)gtT>gtC | p.V350V |
| COADREAD | 8 | 103354750 | 103354750 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6323-01A-11D-1719-10 | TCGA-G4-6323-10A-01D-1720-10 | g.chr8:103354750A>G | c.1049T>C | c.(1048-1050)gTt>gCt | p.V350A |
| COADREAD | 8 | 103354761 | 103354761 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:103354761C>A | c.1038G>T | c.(1036-1038)aaG>aaT | p.K346N |
| COADREAD | 8 | 103354846 | 103354846 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr8:103354846C>T | c.953G>A | c.(952-954)cGt>cAt | p.R318H |
| COADREAD | 8 | 103354869 | 103354869 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr8:103354869T>A | c.930A>T | c.(928-930)gaA>gaT | p.E310D |
| COADREAD | 8 | 103358496 | 103358497 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr8:103358496_103358497insC | c.703_704insG | c.(703-705)gatfs | p.D235fs |
| COADREAD | 8 | 103359252 | 103359252 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-5538-01A-01D-1650-10 | TCGA-D5-5538-10A-02D-1650-10 | g.chr8:103359252C>T | c.455G>A | c.(454-456)cGa>cAa | p.R152Q |
| COADREAD | 8 | 103359262 | 103359262 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr8:103359262C>T | c.445G>A | c.(445-447)Gct>Act | p.A149T |
| COADREAD | 8 | 103372360 | 103372360 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr8:103372360C>T | c.325G>A | c.(325-327)Gac>Aac | p.D109N |
| COADREAD | 8 | 103372382 | 103372382 | + | Silent | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr8:103372382C>T | c.303G>A | c.(301-303)acG>acA | p.T101T |
| COADREAD | 8 | 103373836 | 103373836 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:103373836C>A | c.81G>T | c.(79-81)gaG>gaT | p.E27D |
| DLBC | 8 | 103269903 | 103269903 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FF-8047-01A-11D-2210-10 | TCGA-FF-8047-10A-01D-2210-10 | g.chr8:103269903C>T | c.8144G>A | c.(8143-8145)tGg>tAg | p.W2715* |
| ESCA | 8 | 103269913 | 103269913 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A43I-01A-11D-A247-09 | TCGA-L5-A43I-11A-11D-A247-09 | g.chr8:103269913G>A | c.8134C>T | c.(8134-8136)Cgt>Tgt | p.R2712C |
| ESCA | 8 | 103271268 | 103271268 | + | Silent | SNP | G | G | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr8:103271268G>A | c.8046C>T | c.(8044-8046)tgC>tgT | p.C2682C |
| ESCA | 8 | 103274200 | 103274200 | + | Missense_Mutation | SNP | G | G | C | TCGA-Z6-AAPN-01A-11D-A403-09 | TCGA-Z6-AAPN-10A-01D-A403-09 | g.chr8:103274200G>C | c.7785C>G | c.(7783-7785)ttC>ttG | p.F2595L |
| ESCA | 8 | 103277382 | 103277382 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr8:103277382G>T | c.7547C>A | c.(7546-7548)cCa>cAa | p.P2516Q |
| ESCA | 8 | 103283449 | 103283449 | + | Missense_Mutation | SNP | C | C | T | TCGA-M9-A5M8-01A-11D-A28B-09 | TCGA-M9-A5M8-10A-01D-A28E-09 | g.chr8:103283449C>T | c.6998G>A | c.(6997-6999)cGa>cAa | p.R2333Q |
| ESCA | 8 | 103297931 | 103297931 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr8:103297931G>A | c.5294C>T | c.(5293-5295)gCa>gTa | p.A1765V |
| ESCA | 8 | 103309203 | 103309204 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr8:103309203_103309204insA | c.3582_3583insT | c.(3580-3585)tttgagfs | p.E1195fs |
| GBM | 8 | 103282370 | 103282370 | + | Missense_Mutation | SNP | C | C | A | TCGA-02-0003-01A-01D-1490-08 | TCGA-02-0003-10A-01D-1490-08 | g.chr8:103282370C>A | c.7127G>T | c.(7126-7128)aGa>aTa | p.R2376I |
| GBM | 8 | 103289358 | 103289358 | + | Silent | SNP | C | C | T | TCGA-27-1831-01A-01D-1494-08 | TCGA-27-1831-10A-01D-1494-08 | g.chr8:103289358C>T | c.6351G>A | c.(6349-6351)cgG>cgA | p.R2117R |
| GBM | 8 | 103297923 | 103297923 | + | Missense_Mutation | SNP | C | C | G | TCGA-32-2495-01A-01D-1353-08 | TCGA-32-2495-10B-01D-1353-08 | g.chr8:103297923C>G | c.5302G>C | c.(5302-5304)Gct>Cct | p.A1768P |
| GBM | 8 | 103340098 | 103340099 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-76-6657-01A-11D-1845-08 | TCGA-76-6657-10A-01D-1845-08 | g.chr8:103340098_103340099insA | c.1352_1353insT | c.(1351-1353)ttafs | p.L451fs |
| GBMLGG | 8 | 103266626 | 103266626 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103266626G>A | c.8304C>T | c.(8302-8304)tgC>tgT | p.C2768C |
| GBMLGG | 8 | 103266680 | 103266680 | + | Silent | SNP | G | G | A | TCGA-HT-7857-01A-11D-2395-08 | TCGA-HT-7857-10A-01D-2396-08 | g.chr8:103266680G>A | c.8250C>T | c.(8248-8250)ccC>ccT | p.P2750P |
| GBMLGG | 8 | 103269902 | 103269902 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-S9-A6TV-01A-12D-A34J-08 | TCGA-S9-A6TV-10B-01D-A34M-08 | g.chr8:103269902C>T | c.8145G>A | c.(8143-8145)tgG>tgA | p.W2715* |
| GBMLGG | 8 | 103282370 | 103282370 | + | Missense_Mutation | SNP | C | C | A | TCGA-02-0003-01A-01D-1490-08 | TCGA-02-0003-10A-01D-1490-08 | g.chr8:103282370C>A | c.7127G>T | c.(7126-7128)aGa>aTa | p.R2376I |
| GBMLGG | 8 | 103288036 | 103288036 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103288036C>T | c.6530G>A | c.(6529-6531)gGa>gAa | p.G2177E |
| GBMLGG | 8 | 103289358 | 103289358 | + | Silent | SNP | C | C | T | TCGA-27-1831-01A-01D-1494-08 | TCGA-27-1831-10A-01D-1494-08 | g.chr8:103289358C>T | c.6351G>A | c.(6349-6351)cgG>cgA | p.R2117R |
| GBMLGG | 8 | 103297901 | 103297901 | + | Missense_Mutation | SNP | C | C | T | TCGA-HT-7467-01A-11D-2024-08 | TCGA-HT-7467-10A-01D-2024-08 | g.chr8:103297901C>T | c.5324G>A | c.(5323-5325)aGc>aAc | p.S1775N |
| GBMLGG | 8 | 103297923 | 103297923 | + | Missense_Mutation | SNP | C | C | G | TCGA-32-2495-01A-01D-1353-08 | TCGA-32-2495-10B-01D-1353-08 | g.chr8:103297923C>G | c.5302G>C | c.(5302-5304)Gct>Cct | p.A1768P |
| GBMLGG | 8 | 103312275 | 103312275 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103312275G>T | c.3059C>A | c.(3058-3060)cCc>cAc | p.P1020H |
| GBMLGG | 8 | 103312351 | 103312351 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103312351A>G | c.2983T>C | c.(2983-2985)Tcg>Ccg | p.S995P |
| GBMLGG | 8 | 103327066 | 103327066 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103327066C>A | c.1800G>T | c.(1798-1800)caG>caT | p.Q600H |
| GBMLGG | 8 | 103335639 | 103335639 | + | Missense_Mutation | SNP | T | T | C | TCGA-S9-A89Z-01A-11D-A36O-08 | TCGA-S9-A89Z-10A-01D-A367-08 | g.chr8:103335639T>C | c.1684A>G | c.(1684-1686)Atg>Gtg | p.M562V |
| GBMLGG | 8 | 103340098 | 103340099 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-76-6657-01A-11D-1845-08 | TCGA-76-6657-10A-01D-1845-08 | g.chr8:103340098_103340099insA | c.1352_1353insT | c.(1351-1353)ttafs | p.L451fs |
| GBMLGG | 8 | 103341316 | 103341316 | + | Splice_Site | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103341316A>G | | c.e11+1 | |
| GBMLGG | 8 | 103354859 | 103354859 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103354859C>T | c.940G>A | c.(940-942)Gtt>Att | p.V314I |
| GBMLGG | 8 | 103359284 | 103359284 | + | Silent | SNP | T | T | C | TCGA-DU-6395-01A-12D-1705-08 | TCGA-DU-6395-10A-01D-1705-08 | g.chr8:103359284T>C | c.423A>G | c.(421-423)ggA>ggG | p.G141G |
| HNSC | 8 | 103279210 | 103279210 | + | Missense_Mutation | SNP | C | C | G | TCGA-MT-A67F-01A-11D-A30E-08 | TCGA-MT-A67F-10A-01D-A30H-08 | g.chr8:103279210C>G | c.7387G>C | c.(7387-7389)Gat>Cat | p.D2463H |
| HNSC | 8 | 103281237 | 103281237 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CR-6471-01A-11D-1870-08 | TCGA-CR-6471-10A-01D-1870-08 | g.chr8:103281237C>A | c.7330G>T | c.(7330-7332)Gag>Tag | p.E2444* |
| HNSC | 8 | 103287969 | 103287969 | + | Silent | SNP | T | T | A | TCGA-CV-6950-01A-11D-1912-08 | TCGA-CV-6950-10A-01D-1912-08 | g.chr8:103287969T>A | c.6597A>T | c.(6595-6597)gtA>gtT | p.V2199V |
| HNSC | 8 | 103289202 | 103289202 | + | Silent | SNP | G | G | A | TCGA-CN-4723-01A-01D-1434-08 | TCGA-CN-4723-10A-01D-1434-08 | g.chr8:103289202G>A | c.6507C>T | c.(6505-6507)ttC>ttT | p.F2169F |
| HNSC | 8 | 103291308 | 103291308 | + | Silent | SNP | G | G | A | TCGA-CV-5444-01A-02D-1512-08 | TCGA-CV-5444-11A-01D-1512-08 | g.chr8:103291308G>A | c.6130C>T | c.(6130-6132)Ctg>Ttg | p.L2044L |
| HNSC | 8 | 103293651 | 103293651 | + | Silent | SNP | C | C | T | TCGA-HD-7831-01A-11D-2129-08 | TCGA-HD-7831-10A-01D-2129-08 | g.chr8:103293651C>T | c.5793G>A | c.(5791-5793)gaG>gaA | p.E1931E |
| HNSC | 8 | 103293654 | 103293654 | + | Silent | SNP | A | A | G | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr8:103293654A>G | c.5790T>C | c.(5788-5790)gaT>gaC | p.D1930D |
| HNSC | 8 | 103297762 | 103297762 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-CR-7398-01A-11D-2012-08 | TCGA-CR-7398-10A-01D-2013-08 | g.chr8:103297762G>C | c.5463C>G | c.(5461-5463)taC>taG | p.Y1821* |
| HNSC | 8 | 103301699 | 103301699 | + | Silent | SNP | A | A | T | TCGA-CQ-6221-01A-11D-2078-08 | TCGA-CQ-6221-10A-01D-2078-08 | g.chr8:103301699A>T | c.4695T>A | c.(4693-4695)gtT>gtA | p.V1565V |
| HNSC | 8 | 103305835 | 103305835 | + | Silent | SNP | G | G | A | TCGA-CR-7382-01A-11D-2129-08 | TCGA-CR-7382-10A-01D-2129-08 | g.chr8:103305835G>A | c.4587C>T | c.(4585-4587)agC>agT | p.S1529S |
| HNSC | 8 | 103305964 | 103305964 | + | Silent | SNP | G | G | C | TCGA-CQ-5334-01A-01D-1683-08 | TCGA-CQ-5334-10A-01D-1683-08 | g.chr8:103305964G>C | c.4458C>G | c.(4456-4458)gtC>gtG | p.V1486V |
| HNSC | 8 | 103309160 | 103309160 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7423-01A-11D-2078-08 | TCGA-CV-7423-10A-01D-2078-08 | g.chr8:103309160G>A | c.3626C>T | c.(3625-3627)aCg>aTg | p.T1209M |
| HNSC | 8 | 103310705 | 103310705 | + | Silent | SNP | C | C | T | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr8:103310705C>T | c.3339G>A | c.(3337-3339)ggG>ggA | p.G1113G |
| HNSC | 8 | 103317373 | 103317373 | + | Silent | SNP | A | A | G | TCGA-CV-7425-01A-11D-2078-08 | TCGA-CV-7425-10A-01D-2078-08 | g.chr8:103317373A>G | c.2767T>C | c.(2767-2769)Ttg>Ctg | p.L923L |
| HNSC | 8 | 103323529 | 103323529 | + | Missense_Mutation | SNP | C | C | G | TCGA-CN-4723-01A-01D-1434-08 | TCGA-CN-4723-10A-01D-1434-08 | g.chr8:103323529C>G | c.2614G>C | c.(2614-2616)Gag>Cag | p.E872Q |
| HNSC | 8 | 103324678 | 103324678 | + | Silent | SNP | T | T | C | TCGA-CV-A468-01A-11D-A25Y-08 | TCGA-CV-A468-10A-01D-A25Y-08 | g.chr8:103324678T>C | c.2043A>G | c.(2041-2043)aaA>aaG | p.K681K |
| HNSC | 8 | 103326146 | 103326146 | + | Splice_Site | SNP | T | T | C | TCGA-F7-7848-01A-11D-2129-08 | TCGA-F7-7848-10A-01D-2129-08 | g.chr8:103326146T>C | | c.e16-2 | |
| HNSC | 8 | 103335611 | 103335611 | + | Missense_Mutation | SNP | C | C | A | TCGA-CR-7374-01A-11D-2012-08 | TCGA-CR-7374-10A-01D-2013-08 | g.chr8:103335611C>A | c.1712G>T | c.(1711-1713)aGc>aTc | p.S571I |
| HNSC | 8 | 103338797 | 103338797 | + | Missense_Mutation | SNP | G | G | A | TCGA-BA-A6DI-01A-11D-A30E-08 | TCGA-BA-A6DI-10A-01D-A30H-08 | g.chr8:103338797G>A | c.1576C>T | c.(1576-1578)Ccg>Tcg | p.P526S |
| HNSC | 8 | 103354705 | 103354705 | + | Missense_Mutation | SNP | T | T | C | TCGA-CR-7369-01A-11D-2129-08 | TCGA-CR-7369-10A-01D-2129-08 | g.chr8:103354705T>C | c.1094A>G | c.(1093-1095)gAt>gGt | p.D365G |
| HNSC | 8 | 103354814 | 103354814 | + | Missense_Mutation | SNP | C | C | G | TCGA-QK-A6VC-01A-23D-A34J-08 | TCGA-QK-A6VC-10B-01D-A34M-08 | g.chr8:103354814C>G | c.985G>C | c.(985-987)Gat>Cat | p.D329H |
| HNSC | 8 | 103354904 | 103354904 | + | Missense_Mutation | SNP | G | G | C | TCGA-CQ-7064-01A-11D-2394-08 | TCGA-CQ-7064-10A-01D-2394-08 | g.chr8:103354904G>C | c.895C>G | c.(895-897)Ctt>Gtt | p.L299V |
| HNSC | 8 | 103358499 | 103358499 | + | Missense_Mutation | SNP | C | C | A | TCGA-CN-6988-01A-11D-1912-08 | TCGA-CN-6988-10A-01D-1912-08 | g.chr8:103358499C>A | c.701G>T | c.(700-702)gGg>gTg | p.G234V |
| HNSC | 8 | 103358503 | 103358503 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-6943-01A-11D-1912-08 | TCGA-CV-6943-10A-01D-1912-08 | g.chr8:103358503C>T | c.697G>A | c.(697-699)Gat>Aat | p.D233N |
| HNSC | 8 | 103359213 | 103359213 | + | Missense_Mutation | SNP | C | C | T | TCGA-IQ-A61J-01A-11D-A30E-08 | TCGA-IQ-A61J-10A-01D-A30H-08 | g.chr8:103359213C>T | c.494G>A | c.(493-495)cGg>cAg | p.R165Q |
| HNSC | 8 | 103359220 | 103359220 | + | Missense_Mutation | SNP | T | T | A | TCGA-CV-7438-01A-21D-2129-08 | TCGA-CV-7438-10A-01D-2129-08 | g.chr8:103359220T>A | c.487A>T | c.(487-489)Aca>Tca | p.T163S |
| HNSC | 8 | 103359222 | 103359222 | + | Missense_Mutation | SNP | C | C | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr8:103359222C>T | c.485G>A | c.(484-486)cGg>cAg | p.R162Q |
| HNSC | 8 | 103359282 | 103359282 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-A45Q-01A-11D-A24D-08 | TCGA-CV-A45Q-10A-01D-A24F-08 | g.chr8:103359282C>T | c.425G>A | c.(424-426)gGa>gAa | p.G142E |
| HNSC | 8 | 103359294 | 103359294 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-A45U-01A-12D-A24D-08 | TCGA-CV-A45U-10A-01D-A24F-08 | g.chr8:103359294C>G | c.413G>C | c.(412-414)gGa>gCa | p.G138A |
| HNSC | 8 | 103373366 | 103373366 | + | Missense_Mutation | SNP | G | G | A | TCGA-DQ-5629-01A-01D-1870-08 | TCGA-DQ-5629-10A-01D-1870-08 | g.chr8:103373366G>A | c.176C>T | c.(175-177)gCc>gTc | p.A59V |
| KICH | 8 | 103277497 | 103277497 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-KL-8341-01A-11D-2310-10 | TCGA-KL-8341-11A-01D-2310-10 | g.chr8:103277497G>A | c.7432C>T | c.(7432-7434)Cga>Tga | p.R2478* |
| KICH | 8 | 103324629 | 103324629 | + | Missense_Mutation | SNP | C | C | G | TCGA-KO-8413-01A-11D-2310-10 | TCGA-KO-8413-11A-01D-2311-10 | g.chr8:103324629C>G | c.2092G>C | c.(2092-2094)Gat>Cat | p.D698H |
| KIPAN | 8 | 103266717 | 103266717 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-B0-4693-01A-01D-1361-10 | TCGA-B0-4693-11A-01D-1361-10 | g.chr8:103266717G>T | c.8213C>A | c.(8212-8214)tCa>tAa | p.S2738* |
| KIPAN | 8 | 103266727 | 103266727 | + | Missense_Mutation | SNP | A | A | T | TCGA-V9-A7HT-01A-11D-A33Q-10 | TCGA-V9-A7HT-10A-01D-A33Q-10 | g.chr8:103266727A>T | c.8203T>A | c.(8203-8205)Tca>Aca | p.S2735T |
| KIPAN | 8 | 103273473 | 103273473 | + | Silent | SNP | A | A | T | TCGA-G7-A8LB-01A-11D-A35Z-10 | TCGA-G7-A8LB-10A-01D-A35Z-10 | g.chr8:103273473A>T | c.7857T>A | c.(7855-7857)ccT>ccA | p.P2619P |
| KIPAN | 8 | 103274282 | 103274282 | + | Missense_Mutation | SNP | A | A | T | TCGA-DV-5574-01A-01D-1534-10 | TCGA-DV-5574-10A-01D-1535-10 | g.chr8:103274282A>T | c.7703T>A | c.(7702-7704)tTt>tAt | p.F2568Y |
| KIPAN | 8 | 103277497 | 103277497 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-KL-8341-01A-11D-2310-10 | TCGA-KL-8341-11A-01D-2310-10 | g.chr8:103277497G>A | c.7432C>T | c.(7432-7434)Cga>Tga | p.R2478* |
| KIPAN | 8 | 103297526 | 103297526 | + | Missense_Mutation | SNP | A | A | G | TCGA-CJ-5678-01A-11D-1534-10 | TCGA-CJ-5678-11A-01D-1534-10 | g.chr8:103297526A>G | c.5525T>C | c.(5524-5526)aTg>aCg | p.M1842T |
| KIPAN | 8 | 103324629 | 103324629 | + | Missense_Mutation | SNP | C | C | G | TCGA-KO-8413-01A-11D-2310-10 | TCGA-KO-8413-11A-01D-2311-10 | g.chr8:103324629C>G | c.2092G>C | c.(2092-2094)Gat>Cat | p.D698H |
| KIPAN | 8 | 103327008 | 103327008 | + | Missense_Mutation | SNP | C | C | T | TCGA-EU-5905-01A-11D-1669-08 | TCGA-EU-5905-10A-01D-1669-08 | g.chr8:103327008C>T | c.1858G>A | c.(1858-1860)Gca>Aca | p.A620T |
| KIPAN | 8 | 103341320 | 103341324 | + | Frame_Shift_Del | DEL | TGTTA | TGTTA | - | TCGA-A3-3313-01A-01D-0966-08 | TCGA-A3-3313-11A-01D-0966-08 | g.chr8:103341320_103341324delTGTTA | c.1320_1324delTAACA | c.(1318-1326)aataacaagfs | p.NN440fs |
| KIPAN | 8 | 103341598 | 103341598 | + | Silent | SNP | A | A | G | TCGA-B0-5075-01A-01D-1462-08 | TCGA-B0-5075-11A-01D-1462-08 | g.chr8:103341598A>G | c.1128T>C | c.(1126-1128)gcT>gcC | p.A376A |
| KIPAN | 8 | 103372381 | 103372381 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr8:103372381A>G | c.304T>C | c.(304-306)Tca>Cca | p.S102P |
| KIRC | 8 | 103266717 | 103266717 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-B0-4693-01A-01D-1361-10 | TCGA-B0-4693-11A-01D-1361-10 | g.chr8:103266717G>T | c.8213C>A | c.(8212-8214)tCa>tAa | p.S2738* |
| KIRC | 8 | 103274282 | 103274282 | + | Missense_Mutation | SNP | A | A | T | TCGA-DV-5574-01A-01D-1534-10 | TCGA-DV-5574-10A-01D-1535-10 | g.chr8:103274282A>T | c.7703T>A | c.(7702-7704)tTt>tAt | p.F2568Y |
| KIRC | 8 | 103297526 | 103297526 | + | Missense_Mutation | SNP | A | A | G | TCGA-CJ-5678-01A-11D-1534-10 | TCGA-CJ-5678-11A-01D-1534-10 | g.chr8:103297526A>G | c.5525T>C | c.(5524-5526)aTg>aCg | p.M1842T |
| KIRC | 8 | 103327008 | 103327008 | + | Missense_Mutation | SNP | C | C | T | TCGA-EU-5905-01A-11D-1669-08 | TCGA-EU-5905-10A-01D-1669-08 | g.chr8:103327008C>T | c.1858G>A | c.(1858-1860)Gca>Aca | p.A620T |
| KIRC | 8 | 103341320 | 103341324 | + | Frame_Shift_Del | DEL | TGTTA | TGTTA | - | TCGA-A3-3313-01A-01D-0966-08 | TCGA-A3-3313-11A-01D-0966-08 | g.chr8:103341320_103341324delTGTTA | c.1320_1324delTAACA | c.(1318-1326)aataacaagfs | p.NN440fs |
| KIRC | 8 | 103341598 | 103341598 | + | Silent | SNP | A | A | G | TCGA-B0-5075-01A-01D-1462-08 | TCGA-B0-5075-11A-01D-1462-08 | g.chr8:103341598A>G | c.1128T>C | c.(1126-1128)gcT>gcC | p.A376A |
| KIRC | 8 | 103372381 | 103372381 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr8:103372381A>G | c.304T>C | c.(304-306)Tca>Cca | p.S102P |
| KIRP | 8 | 103266727 | 103266727 | + | Missense_Mutation | SNP | A | A | T | TCGA-V9-A7HT-01A-11D-A33Q-10 | TCGA-V9-A7HT-10A-01D-A33Q-10 | g.chr8:103266727A>T | c.8203T>A | c.(8203-8205)Tca>Aca | p.S2735T |
| KIRP | 8 | 103273473 | 103273473 | + | Silent | SNP | A | A | T | TCGA-G7-A8LB-01A-11D-A35Z-10 | TCGA-G7-A8LB-10A-01D-A35Z-10 | g.chr8:103273473A>T | c.7857T>A | c.(7855-7857)ccT>ccA | p.P2619P |
| LGG | 8 | 103266626 | 103266626 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103266626G>A | c.8304C>T | c.(8302-8304)tgC>tgT | p.C2768C |
| LGG | 8 | 103266680 | 103266680 | + | Silent | SNP | G | G | A | TCGA-HT-7857-01A-11D-2395-08 | TCGA-HT-7857-10A-01D-2396-08 | g.chr8:103266680G>A | c.8250C>T | c.(8248-8250)ccC>ccT | p.P2750P |
| LGG | 8 | 103269902 | 103269902 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-S9-A6TV-01A-12D-A34J-08 | TCGA-S9-A6TV-10B-01D-A34M-08 | g.chr8:103269902C>T | c.8145G>A | c.(8143-8145)tgG>tgA | p.W2715* |
| LGG | 8 | 103288036 | 103288036 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103288036C>T | c.6530G>A | c.(6529-6531)gGa>gAa | p.G2177E |
| LGG | 8 | 103297901 | 103297901 | + | Missense_Mutation | SNP | C | C | T | TCGA-HT-7467-01A-11D-2024-08 | TCGA-HT-7467-10A-01D-2024-08 | g.chr8:103297901C>T | c.5324G>A | c.(5323-5325)aGc>aAc | p.S1775N |
| LGG | 8 | 103312275 | 103312275 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103312275G>T | c.3059C>A | c.(3058-3060)cCc>cAc | p.P1020H |
| LGG | 8 | 103312351 | 103312351 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103312351A>G | c.2983T>C | c.(2983-2985)Tcg>Ccg | p.S995P |
| LGG | 8 | 103327066 | 103327066 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103327066C>A | c.1800G>T | c.(1798-1800)caG>caT | p.Q600H |
| LGG | 8 | 103335639 | 103335639 | + | Missense_Mutation | SNP | T | T | C | TCGA-S9-A89Z-01A-11D-A36O-08 | TCGA-S9-A89Z-10A-01D-A367-08 | g.chr8:103335639T>C | c.1684A>G | c.(1684-1686)Atg>Gtg | p.M562V |
| LGG | 8 | 103341316 | 103341316 | + | Splice_Site | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103341316A>G | | c.e11+1 | |
| LGG | 8 | 103354859 | 103354859 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:103354859C>T | c.940G>A | c.(940-942)Gtt>Att | p.V314I |
| LGG | 8 | 103359284 | 103359284 | + | Silent | SNP | T | T | C | TCGA-DU-6395-01A-12D-1705-08 | TCGA-DU-6395-10A-01D-1705-08 | g.chr8:103359284T>C | c.423A>G | c.(421-423)ggA>ggG | p.G141G |
| LIHC | 8 | 103293516 | 103293516 | + | Splice_Site | SNP | C | C | T | TCGA-DD-A1EF-01A-11D-A12Z-10 | TCGA-DD-A1EF-10A-01D-A12Z-10 | g.chr8:103293516C>T | | c.e41+1 | |
| LIHC | 8 | 103300480 | 103300480 | + | Silent | SNP | C | C | T | TCGA-BC-A3KF-01A-11D-A20W-10 | TCGA-BC-A3KF-10A-01D-A20W-10 | g.chr8:103300480C>T | c.4728G>A | c.(4726-4728)gaG>gaA | p.E1576E |
| LIHC | 8 | 103324043 | 103324043 | + | Missense_Mutation | SNP | G | G | C | TCGA-DD-A4NJ-01A-11D-A27I-10 | TCGA-DD-A4NJ-10A-01D-A27I-10 | g.chr8:103324043G>C | c.2338C>G | c.(2338-2340)Cag>Gag | p.Q780E |
| LIHC | 8 | 103335715 | 103335715 | + | Missense_Mutation | SNP | C | C | G | TCGA-CC-A9FU-01A-11D-A36X-10 | TCGA-CC-A9FU-10A-01D-A370-10 | g.chr8:103335715C>G | c.1608G>C | c.(1606-1608)ttG>ttC | p.L536F |
| LUAD | 8 | 103273473 | 103273473 | + | Silent | SNP | A | A | G | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr8:103273473A>G | c.7857T>C | c.(7855-7857)ccT>ccC | p.P2619P |
| LUAD | 8 | 103277369 | 103277369 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr8:103277369C>G | c.7560G>C | c.(7558-7560)aaG>aaC | p.K2520N |
| LUAD | 8 | 103277397 | 103277397 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-6851-01A-11D-1945-08 | TCGA-86-6851-10A-01D-1946-08 | g.chr8:103277397C>G | c.7532G>C | c.(7531-7533)aGa>aCa | p.R2511T |
| LUAD | 8 | 103277449 | 103277449 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr8:103277449C>T | c.7480G>A | c.(7480-7482)Gat>Aat | p.D2494N |
| LUAD | 8 | 103282300 | 103282300 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8089-01A-11D-2238-08 | TCGA-55-8089-10A-01D-2238-08 | g.chr8:103282300C>A | c.7197G>T | c.(7195-7197)gaG>gaT | p.E2399D |
| LUAD | 8 | 103284883 | 103284883 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr8:103284883C>A | c.6847G>T | c.(6847-6849)Gat>Tat | p.D2283Y |
| LUAD | 8 | 103287796 | 103287796 | + | Missense_Mutation | SNP | C | C | T | TCGA-64-1681-01A-11D-2063-08 | TCGA-64-1681-10A-01D-2063-08 | g.chr8:103287796C>T | c.6682G>A | c.(6682-6684)Gaa>Aaa | p.E2228K |
| LUAD | 8 | 103287962 | 103287962 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-44-5644-01A-21D-2036-08 | TCGA-44-5644-10A-01D-2036-08 | g.chr8:103287962C>A | c.6604G>T | c.(6604-6606)Gaa>Taa | p.E2202* |
| LUAD | 8 | 103289393 | 103289393 | + | Missense_Mutation | SNP | C | C | T | TCGA-L4-A4E5-01A-11D-A24P-08 | TCGA-L4-A4E5-10A-01D-A24P-08 | g.chr8:103289393C>T | c.6316G>A | c.(6316-6318)Gcc>Acc | p.A2106T |
| LUAD | 8 | 103291157 | 103291157 | + | Missense_Mutation | SNP | C | C | G | TCGA-05-4402-01A-01D-1265-08 | TCGA-05-4402-10A-01D-1265-08 | g.chr8:103291157C>G | c.6185G>C | c.(6184-6186)aGa>aCa | p.R2062T |
| LUAD | 8 | 103293656 | 103293656 | + | Missense_Mutation | SNP | C | C | T | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr8:103293656C>T | c.5788G>A | c.(5788-5790)Gat>Aat | p.D1930N |
| LUAD | 8 | 103297392 | 103297392 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-97-7937-01A-11D-2167-08 | TCGA-97-7937-10A-01D-2167-08 | g.chr8:103297392G>A | c.5659C>T | c.(5659-5661)Cga>Tga | p.R1887* |
| LUAD | 8 | 103298663 | 103298663 | + | Missense_Mutation | SNP | T | T | G | TCGA-44-8120-01A-11D-2238-08 | TCGA-44-8120-10A-01D-2238-08 | g.chr8:103298663T>G | c.5140A>C | c.(5140-5142)Atg>Ctg | p.M1714L |
| LUAD | 8 | 103298773 | 103298773 | + | Missense_Mutation | SNP | C | C | T | TCGA-78-8662-01A-11D-2393-08 | TCGA-78-8662-10A-01D-2393-08 | g.chr8:103298773C>T | c.5030G>A | c.(5029-5031)aGt>aAt | p.S1677N |
| LUAD | 8 | 103301722 | 103301722 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr8:103301722C>A | c.4672G>T | c.(4672-4674)Gat>Tat | p.D1558Y |
| LUAD | 8 | 103306336 | 103306336 | + | Missense_Mutation | SNP | T | T | A | TCGA-95-A4VP-01A-21D-A25L-08 | TCGA-95-A4VP-10A-01D-A25L-08 | g.chr8:103306336T>A | c.4196A>T | c.(4195-4197)gAt>gTt | p.D1399V |
| LUAD | 8 | 103309166 | 103309166 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-7159-01A-11D-2036-08 | TCGA-78-7159-10A-01D-2036-08 | g.chr8:103309166C>A | c.3620G>T | c.(3619-3621)tGt>tTt | p.C1207F |
| LUAD | 8 | 103311753 | 103311753 | + | Silent | SNP | C | C | A | TCGA-86-8585-01A-11D-2393-08 | TCGA-86-8585-10A-01D-2393-08 | g.chr8:103311753C>A | c.3129G>T | c.(3127-3129)ctG>ctT | p.L1043L |
| LUAD | 8 | 103316347 | 103316347 | + | Missense_Mutation | SNP | C | C | T | TCGA-50-5066-01A-01D-1625-08 | TCGA-50-5066-10A-01D-1625-08 | g.chr8:103316347C>T | c.2878G>A | c.(2878-2880)Gag>Aag | p.E960K |
| LUAD | 8 | 103316394 | 103316394 | + | Missense_Mutation | SNP | G | G | A | TCGA-MP-A4TA-01A-21D-A24P-08 | TCGA-MP-A4TA-10A-01D-A24P-08 | g.chr8:103316394G>A | c.2831C>T | c.(2830-2832)gCg>gTg | p.A944V |
| LUAD | 8 | 103317388 | 103317388 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-8358-01A-11D-2323-08 | TCGA-86-8358-10A-01D-2323-08 | g.chr8:103317388C>G | c.2752G>C | c.(2752-2754)Gga>Cga | p.G918R |
| LUAD | 8 | 103317410 | 103317410 | + | Silent | SNP | T | T | C | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr8:103317410T>C | c.2730A>G | c.(2728-2730)acA>acG | p.T910T |
| LUAD | 8 | 103324705 | 103324705 | + | Missense_Mutation | SNP | T | T | G | TCGA-67-6215-01A-11D-1753-08 | TCGA-67-6215-10A-01D-1753-08 | g.chr8:103324705T>G | c.2016A>C | c.(2014-2016)aaA>aaC | p.K672N |
| LUAD | 8 | 103327008 | 103327008 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr8:103327008C>A | c.1858G>T | c.(1858-1860)Gca>Tca | p.A620S |
| LUAD | 8 | 103338891 | 103338891 | + | Splice_Site | SNP | C | C | A | TCGA-17-Z025-01A-01W-0746-08 | TCGA-17-Z025-11A-01W-0746-08 | g.chr8:103338891C>A | c.1482G>T | c.(1480-1482)tgG>tgT | p.W494C |
| LUAD | 8 | 103339998 | 103339998 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-8255-01A-11D-2284-08 | TCGA-69-8255-10A-01D-2284-08 | g.chr8:103339998C>A | c.1453G>T | c.(1453-1455)Gct>Tct | p.A485S |
| LUAD | 8 | 103341407 | 103341407 | + | Missense_Mutation | SNP | G | G | C | TCGA-91-6848-01A-11D-1945-08 | TCGA-91-6848-11A-01D-1945-08 | g.chr8:103341407G>C | c.1237C>G | c.(1237-1239)Cga>Gga | p.R413G |
| LUAD | 8 | 103354709 | 103354709 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr8:103354709G>A | c.1090C>T | c.(1090-1092)Cct>Tct | p.P364S |
| LUAD | 8 | 103357641 | 103357641 | + | Missense_Mutation | SNP | C | C | A | TCGA-NJ-A4YF-01A-12D-A25L-08 | TCGA-NJ-A4YF-10A-01D-A25L-08 | g.chr8:103357641C>A | c.869G>T | c.(868-870)aGg>aTg | p.R290M |
| LUAD | 8 | 103358466 | 103358466 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-8585-01A-11D-2393-08 | TCGA-86-8585-10A-01D-2393-08 | g.chr8:103358466C>T | c.734G>A | c.(733-735)gGa>gAa | p.G245E |
| LUAD | 8 | 103358521 | 103358521 | + | Missense_Mutation | SNP | C | C | T | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr8:103358521C>T | c.679G>A | c.(679-681)Gat>Aat | p.D227N |
| LUAD | 8 | 103359295 | 103359295 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-38-4631-01A-01D-1753-08 | TCGA-38-4631-11A-01D-1753-08 | g.chr8:103359295C>A | c.412G>T | c.(412-414)Gga>Tga | p.G138* |
| LUSC | 8 | 103274250 | 103274250 | + | Silent | SNP | A | A | G | TCGA-39-5030-01A-01D-1441-08 | TCGA-39-5030-11A-01D-1441-08 | g.chr8:103274250A>G | c.7735T>C | c.(7735-7737)Ttg>Ctg | p.L2579L |
| LUSC | 8 | 103284843 | 103284843 | + | Missense_Mutation | SNP | T | T | C | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr8:103284843T>C | c.6887A>G | c.(6886-6888)tAt>tGt | p.Y2296C |
| LUSC | 8 | 103297515 | 103297515 | + | Missense_Mutation | SNP | T | T | C | TCGA-66-2754-01A-01D-0983-08 | TCGA-66-2754-11A-01D-0983-08 | g.chr8:103297515T>C | c.5536A>G | c.(5536-5538)Atg>Gtg | p.M1846V |
| LUSC | 8 | 103298627 | 103298627 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2759-01A-01D-1522-08 | TCGA-66-2759-11A-01D-1522-08 | g.chr8:103298627C>A | c.5176G>T | c.(5176-5178)Gca>Tca | p.A1726S |
| LUSC | 8 | 103299699 | 103299699 | + | Missense_Mutation | SNP | C | C | G | TCGA-21-5782-01A-01D-1632-08 | TCGA-21-5782-10A-01D-1632-08 | g.chr8:103299699C>G | c.4919G>C | c.(4918-4920)aGa>aCa | p.R1640T |
| LUSC | 8 | 103299702 | 103299702 | + | Missense_Mutation | SNP | C | C | G | TCGA-18-3410-01A-01D-0983-08 | TCGA-18-3410-11A-01D-0983-08 | g.chr8:103299702C>G | c.4916G>C | c.(4915-4917)cGc>cCc | p.R1639P |
| LUSC | 8 | 103301779 | 103301779 | + | Missense_Mutation | SNP | T | T | C | TCGA-66-2734-01A-01D-0983-08 | TCGA-66-2734-11A-01D-0983-08 | g.chr8:103301779T>C | c.4615A>G | c.(4615-4617)Atc>Gtc | p.I1539V |
| LUSC | 8 | 103306322 | 103306322 | + | Missense_Mutation | SNP | T | T | A | TCGA-43-5668-01A-01D-1632-08 | TCGA-43-5668-11A-01D-1632-08 | g.chr8:103306322T>A | c.4210A>T | c.(4210-4212)Aca>Tca | p.T1404S |
| LUSC | 8 | 103309124 | 103309124 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2792-01A-01D-0983-08 | TCGA-66-2792-11A-01D-0983-08 | g.chr8:103309124C>A | c.3662G>T | c.(3661-3663)tGc>tTc | p.C1221F |
| LUSC | 8 | 103312247 | 103312247 | + | Silent | SNP | G | G | A | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr8:103312247G>A | c.3087C>T | c.(3085-3087)gaC>gaT | p.D1029D |
| LUSC | 8 | 103324640 | 103324640 | + | Missense_Mutation | SNP | C | C | A | TCGA-33-4566-01A-01D-1441-08 | TCGA-33-4566-11A-01D-1441-08 | g.chr8:103324640C>A | c.2081G>T | c.(2080-2082)aGc>aTc | p.S694I |
| LUSC | 8 | 103340026 | 103340026 | + | Silent | SNP | A | A | T | TCGA-66-2777-01A-01D-1267-08 | TCGA-66-2777-11A-01D-1267-08 | g.chr8:103340026A>T | c.1425T>A | c.(1423-1425)tcT>tcA | p.S475S |
| LUSC | 8 | 103341406 | 103341406 | + | Missense_Mutation | SNP | C | C | A | TCGA-85-6561-01A-11D-1817-08 | TCGA-85-6561-10A-01D-1817-08 | g.chr8:103341406C>A | c.1238G>T | c.(1237-1239)cGa>cTa | p.R413L |
| LUSC | 8 | 103359276 | 103359276 | + | Missense_Mutation | SNP | G | G | T | TCGA-85-6561-01A-11D-1817-08 | TCGA-85-6561-10A-01D-1817-08 | g.chr8:103359276G>T | c.431C>A | c.(430-432)tCt>tAt | p.S144Y |
| OV | 8 | 103271255 | 103271255 | + | Missense_Mutation | SNP | C | C | T | TCGA-61-1738-01A-01W-0639-09 | TCGA-61-1738-11A-01W-0639-09 | g.chr8:103271255C>T | c.8059G>A | c.(8059-8061)Gtg>Atg | p.V2687M |
| OV | 8 | 103277451 | 103277451 | + | Missense_Mutation | SNP | T | T | A | TCGA-13-0905-01B-01W-0492-08 | TCGA-13-0905-10A-01W-0492-08 | g.chr8:103277451T>A | c.7478A>T | c.(7477-7479)gAt>gTt | p.D2493V |
| OV | 8 | 103298812 | 103298812 | + | Missense_Mutation | SNP | T | T | C | TCGA-61-1727-01A-01W-0639-09 | TCGA-61-1727-11A-01W-0639-09 | g.chr8:103298812T>C | c.4991A>G | c.(4990-4992)gAt>gGt | p.D1664G |
| OV | 8 | 103317451 | 103317451 | + | Missense_Mutation | SNP | G | G | T | TCGA-36-2543-01A-01D-1526-09 | TCGA-36-2543-10A-01D-1526-09 | g.chr8:103317451G>T | c.2689C>A | c.(2689-2691)Caa>Aaa | p.Q897K |
| OV | 8 | 103323725 | 103323725 | + | Splice_Site | SNP | C | C | T | TCGA-13-0720-01A-01W-0370-10 | TCGA-13-0720-10B-01W-0370-10 | g.chr8:103323725C>T | | c.e20-1 | |
| OV | 8 | 103354762 | 103354762 | + | Missense_Mutation | SNP | T | T | C | TCGA-30-1862-01A-02W-0699-08 | TCGA-30-1862-10A-01W-0699-08 | g.chr8:103354762T>C | c.1037A>G | c.(1036-1038)aAg>aGg | p.K346R |
| OV | 8 | 103354864 | 103354864 | + | Missense_Mutation | SNP | T | T | G | TCGA-10-0927-01A-02W-0419-10 | TCGA-10-0927-11A-01W-0419-10 | g.chr8:103354864T>G | c.935A>C | c.(934-936)gAa>gCa | p.E312A |
| PAAD | 8 | 103266610 | 103266610 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr8:103266610C>T | c.8320G>A | c.(8320-8322)Gtc>Atc | p.V2774I |
| PAAD | 8 | 103274267 | 103274267 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr8:103274267G>T | c.7718C>A | c.(7717-7719)cCt>cAt | p.P2573H |
| PAAD | 8 | 103307906 | 103307906 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr8:103307906C>T | c.3770G>A | c.(3769-3771)cGc>cAc | p.R1257H |
| PAAD | 8 | 103338880 | 103338880 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr8:103338880G>A | c.1493C>T | c.(1492-1494)cCt>cTt | p.P498L |
| PAAD | 8 | 103357683 | 103357683 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr8:103357683C>A | c.827G>T | c.(826-828)aGc>aTc | p.S276I |
| PRAD | 8 | 103291134 | 103291134 | + | Missense_Mutation | SNP | G | G | T | TCGA-VN-A88O-01A-11D-A34U-08 | TCGA-VN-A88O-10A-01D-A34X-08 | g.chr8:103291134G>T | c.6208C>A | c.(6208-6210)Cca>Aca | p.P2070T |
| PRAD | 8 | 103291368 | 103291368 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-G9-7519-01A-11D-2260-08 | TCGA-G9-7519-10A-01D-2260-08 | g.chr8:103291368G>A | c.6070C>T | c.(6070-6072)Cga>Tga | p.R2024* |
| PRAD | 8 | 103293668 | 103293668 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr8:103293668G>A | c.5776C>T | c.(5776-5778)Cgg>Tgg | p.R1926W |
| PRAD | 8 | 103298847 | 103298847 | + | Splice_Site | SNP | T | T | C | TCGA-EJ-7791-01A-11D-2114-08 | TCGA-EJ-7791-10A-01D-2115-08 | g.chr8:103298847T>C | | c.e38-2 | |
| PRAD | 8 | 103310685 | 103310685 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr8:103310685G>A | c.3359C>T | c.(3358-3360)gCt>gTt | p.A1120V |
| PRAD | 8 | 103317441 | 103317441 | + | Missense_Mutation | SNP | A | A | G | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr8:103317441A>G | c.2699T>C | c.(2698-2700)gTt>gCt | p.V900A |
| READ | 8 | 103266662 | 103266662 | + | Silent | SNP | T | T | G | TCGA-CL-5917-01A-11D-1657-10 | TCGA-CL-5917-10A-01D-1657-10 | g.chr8:103266662T>G | c.8268A>C | c.(8266-8268)ccA>ccC | p.P2756P |
| READ | 8 | 103269876 | 103269876 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3575-01A-01W-0831-10 | TCGA-AG-3575-10A-01W-0831-10 | g.chr8:103269876G>A | c.8171C>T | c.(8170-8172)aCa>aTa | p.T2724I |
| READ | 8 | 103284867 | 103284867 | + | Missense_Mutation | SNP | C | C | T | TCGA-F5-6465-01A-11D-1733-10 | TCGA-F5-6465-10A-01D-1733-10 | g.chr8:103284867C>T | c.6863G>A | c.(6862-6864)gGc>gAc | p.G2288D |
| READ | 8 | 103291365 | 103291365 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr8:103291365G>A | c.6073C>T | c.(6073-6075)Cgt>Tgt | p.R2025C |
| READ | 8 | 103299706 | 103299706 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3999-01A-01W-1073-09 | TCGA-AG-3999-10A-01W-1073-09 | g.chr8:103299706C>T | c.4912G>A | c.(4912-4914)Ggg>Agg | p.G1638R |
| READ | 8 | 103317375 | 103317375 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3584-01A-01W-0831-10 | TCGA-AG-3584-10A-01W-0831-10 | g.chr8:103317375A>C | c.2765T>G | c.(2764-2766)aTt>aGt | p.I922S |
| READ | 8 | 103317461 | 103317461 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:103317461C>A | c.2679G>T | c.(2677-2679)atG>atT | p.M893I |
| READ | 8 | 103341610 | 103341610 | + | Silent | SNP | G | G | A | TCGA-AG-3612-01A-01W-0833-10 | TCGA-AG-3612-10A-01W-0833-10 | g.chr8:103341610G>A | c.1116C>T | c.(1114-1116)atC>atT | p.I372I |
| READ | 8 | 103354761 | 103354761 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:103354761C>A | c.1038G>T | c.(1036-1038)aaG>aaT | p.K346N |
| READ | 8 | 103373836 | 103373836 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:103373836C>A | c.81G>T | c.(79-81)gaG>gaT | p.E27D |
| SKCM | 8 | 103266681 | 103266681 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JI-06A-11D-A21A-08 | TCGA-EE-A3JI-10A-01D-A21A-08 | g.chr8:103266681G>A | c.8249C>T | c.(8248-8250)cCc>cTc | p.P2750L |
| SKCM | 8 | 103269903 | 103269903 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr8:103269903C>T | c.8144G>A | c.(8143-8145)tGg>tAg | p.W2715* |
| SKCM | 8 | 103271215 | 103271215 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr8:103271215G>A | c.8099C>T | c.(8098-8100)tCa>tTa | p.S2700L |
| SKCM | 8 | 103271215 | 103271215 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr8:103271215G>T | c.8099C>A | c.(8098-8100)tCa>tAa | p.S2700* |
| SKCM | 8 | 103271216 | 103271216 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr8:103271216A>T | c.8098T>A | c.(8098-8100)Tca>Aca | p.S2700T |
| SKCM | 8 | 103274169 | 103274169 | + | Missense_Mutation | SNP | G | G | C | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr8:103274169G>C | c.7816C>G | c.(7816-7818)Ctg>Gtg | p.L2606V |
| SKCM | 8 | 103274276 | 103274276 | + | Missense_Mutation | SNP | A | A | C | TCGA-EE-A3J8-06A-11D-A20D-08 | TCGA-EE-A3J8-10A-01D-A20D-08 | g.chr8:103274276A>C | c.7709T>G | c.(7708-7710)tTt>tGt | p.F2570C |
| SKCM | 8 | 103279190 | 103279190 | + | Silent | SNP | G | G | A | TCGA-EE-A2GN-06A-11D-A196-08 | TCGA-EE-A2GN-10A-01D-A198-08 | g.chr8:103279190G>A | c.7407C>T | c.(7405-7407)tcC>tcT | p.S2469S |
| SKCM | 8 | 103289399 | 103289399 | + | Missense_Mutation | SNP | A | A | G | TCGA-FR-A3YN-06A-11D-A23B-08 | TCGA-FR-A3YN-10A-01D-A23B-08 | g.chr8:103289399A>G | c.6310T>C | c.(6310-6312)Tat>Cat | p.Y2104H |
| SKCM | 8 | 103291105 | 103291105 | + | Silent | SNP | G | G | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr8:103291105G>T | c.6237C>A | c.(6235-6237)gcC>gcA | p.A2079A |
| SKCM | 8 | 103293623 | 103293623 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr8:103293623C>T | c.5821G>A | c.(5821-5823)Gtt>Att | p.V1941I |
| SKCM | 8 | 103297818 | 103297818 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr8:103297818G>A | c.5407C>T | c.(5407-5409)Cct>Tct | p.P1803S |
| SKCM | 8 | 103306290 | 103306290 | + | Silent | SNP | T | T | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr8:103306290T>A | c.4242A>T | c.(4240-4242)acA>acT | p.T1414T |
| SKCM | 8 | 103307719 | 103307719 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr8:103307719C>T | c.3854G>A | c.(3853-3855)aGg>aAg | p.R1285K |
| SKCM | 8 | 103307739 | 103307739 | + | Silent | SNP | G | G | A | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr8:103307739G>A | c.3834C>T | c.(3832-3834)ttC>ttT | p.F1278F |
| SKCM | 8 | 103307750 | 103307750 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr8:103307750G>A | c.3823C>T | c.(3823-3825)Ctc>Ttc | p.L1275F |
| SKCM | 8 | 103308007 | 103308007 | + | Silent | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr8:103308007G>A | c.3669C>T | c.(3667-3669)ctC>ctT | p.L1223L |
| SKCM | 8 | 103311078 | 103311078 | + | Silent | SNP | G | G | A | TCGA-EE-A29C-06A-21D-A197-08 | TCGA-EE-A29C-10A-01D-A199-08 | g.chr8:103311078G>A | c.3324C>T | c.(3322-3324)gcC>gcT | p.A1108A |
| SKCM | 8 | 103311161 | 103311161 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr8:103311161G>A | c.3241C>T | c.(3241-3243)Cga>Tga | p.R1081* |
| SKCM | 8 | 103311700 | 103311700 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr8:103311700G>A | c.3182C>T | c.(3181-3183)cCa>cTa | p.P1061L |
| SKCM | 8 | 103311701 | 103311701 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr8:103311701G>A | c.3181C>T | c.(3181-3183)Cca>Tca | p.P1061S |
| SKCM | 8 | 103316393 | 103316393 | + | Silent | SNP | C | C | A | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr8:103316393C>A | c.2832G>T | c.(2830-2832)gcG>gcT | p.A944A |
| SKCM | 8 | 103317392 | 103317392 | + | Missense_Mutation | SNP | A | A | C | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr8:103317392A>C | c.2748T>G | c.(2746-2748)tgT>tgG | p.C916W |
| SKCM | 8 | 103323563 | 103323563 | + | Silent | SNP | G | G | A | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr8:103323563G>A | c.2580C>T | c.(2578-2580)atC>atT | p.I860I |
| SKCM | 8 | 103323718 | 103323718 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr8:103323718G>A | c.2425C>T | c.(2425-2427)Ccc>Tcc | p.P809S |
| SKCM | 8 | 103324674 | 103324674 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GP-06A-11D-A197-08 | TCGA-EE-A2GP-10A-01D-A199-08 | g.chr8:103324674G>A | c.2047C>T | c.(2047-2049)Cca>Tca | p.P683S |
| SKCM | 8 | 103326079 | 103326079 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr8:103326079G>A | c.1960C>T | c.(1960-1962)Cgg>Tgg | p.R654W |
| SKCM | 8 | 103338881 | 103338881 | + | Missense_Mutation | SNP | G | G | C | TCGA-EE-A29C-06A-21D-A197-08 | TCGA-EE-A29C-10A-01D-A199-08 | g.chr8:103338881G>C | c.1492C>G | c.(1492-1494)Cct>Gct | p.P498A |
| SKCM | 8 | 103340049 | 103340049 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr8:103340049G>A | c.1402C>T | c.(1402-1404)Ctt>Ttt | p.L468F |
| SKCM | 8 | 103354800 | 103354800 | + | Silent | SNP | A | A | G | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr8:103354800A>G | c.999T>C | c.(997-999)ggT>ggC | p.G333G |
| SKCM | 8 | 103359151 | 103359151 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3C3-06A-12D-A19A-08 | TCGA-D3-A3C3-10A-01D-A19A-08 | g.chr8:103359151G>A | c.556C>T | c.(556-558)Cca>Tca | p.P186S |
| SKCM | 8 | 103359165 | 103359165 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr8:103359165G>A | c.542C>T | c.(541-543)cCa>cTa | p.P181L |
| SKCM | 8 | 103372302 | 103372302 | + | Missense_Mutation | SNP | A | A | G | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr8:103372302A>G | c.383T>C | c.(382-384)tTa>tCa | p.L128S |