| 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 | 4 | 177061126 | 177061126 | + | Splice_Site | SNP | G | G | T | TCGA-OR-A5L6-01A-11D-A29I-10 | TCGA-OR-A5L6-10C-01D-A29L-10 | g.chr4:177061126G>T | | c.e11+1 | |
| ACC | 4 | 177098263 | 177098263 | + | Silent | SNP | T | T | A | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr4:177098263T>A | c.3621T>A | c.(3619-3621)tcT>tcA | p.S1207S |
| BLCA | 4 | 177032776 | 177032776 | + | Missense_Mutation | SNP | G | G | T | TCGA-FD-A6TG-01A-11D-A32B-08 | TCGA-FD-A6TG-10A-01D-A329-08 | g.chr4:177032776G>T | c.117G>T | c.(115-117)caG>caT | p.Q39H |
| BLCA | 4 | 177037064 | 177037064 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9SK-01A-11D-A42E-08 | TCGA-XF-A9SK-10A-01D-A42H-08 | g.chr4:177037064G>A | c.313G>A | c.(313-315)Gat>Aat | p.D105N |
| BLCA | 4 | 177041056 | 177041056 | + | Missense_Mutation | SNP | G | G | A | TCGA-4Z-AA86-01A-11D-A391-08 | TCGA-4Z-AA86-10A-01D-A394-08 | g.chr4:177041056G>A | c.418G>A | c.(418-420)Gat>Aat | p.D140N |
| BLCA | 4 | 177052851 | 177052851 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-AA53-01A-11D-A391-08 | TCGA-ZF-AA53-10A-01D-A394-08 | g.chr4:177052851G>A | c.1132G>A | c.(1132-1134)Gat>Aat | p.D378N |
| BLCA | 4 | 177052884 | 177052884 | + | Missense_Mutation | SNP | G | G | C | TCGA-BT-A0YX-01A-11D-A10S-08 | TCGA-BT-A0YX-10A-01D-A10S-08 | g.chr4:177052884G>C | c.1165G>C | c.(1165-1167)Gac>Cac | p.D389H |
| BLCA | 4 | 177058703 | 177058703 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FJ-A3Z7-01A-12D-A23M-08 | TCGA-FJ-A3Z7-10A-01D-A23K-08 | g.chr4:177058703C>T | c.1372C>T | c.(1372-1374)Cga>Tga | p.R458* |
| BLCA | 4 | 177081163 | 177081163 | + | Missense_Mutation | SNP | C | C | G | TCGA-ZF-A9R1-01A-11D-A391-08 | TCGA-ZF-A9R1-10A-01D-A394-08 | g.chr4:177081163C>G | c.2616C>G | c.(2614-2616)atC>atG | p.I872M |
| BLCA | 4 | 177083257 | 177083257 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr4:177083257G>T | c.2854G>T | c.(2854-2856)Gaa>Taa | p.E952* |
| BLCA | 4 | 177083305 | 177083305 | + | Missense_Mutation | SNP | C | C | T | TCGA-E5-A4U1-01A-11D-A31L-08 | TCGA-E5-A4U1-10B-01D-A31J-08 | g.chr4:177083305C>T | c.2902C>T | c.(2902-2904)Ctt>Ttt | p.L968F |
| BLCA | 4 | 177089822 | 177089822 | + | Missense_Mutation | SNP | G | G | A | TCGA-GV-A3QI-01A-11D-A21Z-08 | TCGA-GV-A3QI-10A-01D-A21Z-08 | g.chr4:177089822G>A | c.3107G>A | c.(3106-3108)aGg>aAg | p.R1036K |
| BLCA | 4 | 177093544 | 177093544 | + | Missense_Mutation | SNP | G | G | C | TCGA-4Z-AA86-01A-11D-A391-08 | TCGA-4Z-AA86-10A-01D-A394-08 | g.chr4:177093544G>C | c.3238G>C | c.(3238-3240)Gaa>Caa | p.E1080Q |
| BLCA | 4 | 177093565 | 177093565 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A7DU-01A-11D-A32B-08 | TCGA-E7-A7DU-10A-01D-A329-08 | g.chr4:177093565G>A | c.3259G>A | c.(3259-3261)Gag>Aag | p.E1087K |
| BLCA | 4 | 177093648 | 177093648 | + | Missense_Mutation | SNP | T | T | G | TCGA-S5-AA26-01A-11D-A38G-08 | TCGA-S5-AA26-10A-01D-A38J-08 | g.chr4:177093648T>G | c.3342T>G | c.(3340-3342)atT>atG | p.I1114M |
| BLCA | 4 | 177098267 | 177098267 | + | Missense_Mutation | SNP | G | G | A | TCGA-FJ-A3ZE-01A-11D-A23M-08 | TCGA-FJ-A3ZE-10A-01D-A23K-08 | g.chr4:177098267G>A | c.3625G>A | c.(3625-3627)Gaa>Aaa | p.E1209K |
| BLCA | 4 | 177098691 | 177098691 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A3X1-01A-12D-A22Z-08 | TCGA-DK-A3X1-10A-01D-A22Z-08 | g.chr4:177098691G>C | c.3735G>C | c.(3733-3735)aaG>aaC | p.K1245N |
| BLCA | 4 | 177100727 | 177100727 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9SM-01A-11D-A42E-08 | TCGA-XF-A9SM-10A-01D-A42H-08 | g.chr4:177100727C>G | c.3966C>G | c.(3964-3966)ttC>ttG | p.F1322L |
| BRCA | 4 | 177032726 | 177032726 | + | Splice_Site | SNP | G | G | A | TCGA-LL-A5YL-01A-12D-A29N-09 | TCGA-LL-A5YL-10A-01D-A29N-09 | g.chr4:177032726G>A | c.67G>A | c.(67-69)Gca>Aca | p.A23T |
| BRCA | 4 | 177032810 | 177032810 | + | Missense_Mutation | SNP | G | G | A | TCGA-GM-A2D9-01A-11D-A18P-09 | TCGA-GM-A2D9-11A-42D-A18P-09 | g.chr4:177032810G>A | c.151G>A | c.(151-153)Gac>Aac | p.D51N |
| BRCA | 4 | 177036997 | 177036998 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AO-A124-01A-11D-A10M-09 | TCGA-AO-A124-10A-01D-A10M-09 | g.chr4:177036997_177036998insA | c.246_247insA | c.(247-249)aaafs | p.K83fs |
| BRCA | 4 | 177041169 | 177041169 | + | Silent | SNP | T | T | C | TCGA-A7-A3J0-01A-11D-A20S-09 | TCGA-A7-A3J0-10A-01D-A20S-09 | g.chr4:177041169T>C | c.531T>C | c.(529-531)tgT>tgC | p.C177C |
| BRCA | 4 | 177041218 | 177041218 | + | Missense_Mutation | SNP | A | A | C | TCGA-AN-A0FD-01A-11W-A050-09 | TCGA-AN-A0FD-10A-01W-A055-09 | g.chr4:177041218A>C | c.580A>C | c.(580-582)Att>Ctt | p.I194L |
| BRCA | 4 | 177046468 | 177046468 | + | Missense_Mutation | SNP | C | C | T | TCGA-C8-A12P-01A-11D-A10Y-09 | TCGA-C8-A12P-10A-01D-A110-09 | g.chr4:177046468C>T | c.824C>T | c.(823-825)gCc>gTc | p.A275V |
| BRCA | 4 | 177049888 | 177049888 | + | Splice_Site | SNP | G | G | C | TCGA-E2-A159-01A-11D-A10Y-09 | TCGA-E2-A159-10A-01D-A110-09 | g.chr4:177049888G>C | | c.e7-1 | |
| BRCA | 4 | 177050008 | 177050008 | + | Missense_Mutation | SNP | A | A | G | TCGA-E9-A1NF-01A-11D-A14G-09 | TCGA-E9-A1NF-10A-01D-A14G-09 | g.chr4:177050008A>G | c.982A>G | c.(982-984)Aag>Gag | p.K328E |
| BRCA | 4 | 177052721 | 177052721 | + | Silent | SNP | A | A | G | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr4:177052721A>G | c.1002A>G | c.(1000-1002)ccA>ccG | p.P334P |
| BRCA | 4 | 177071638 | 177071638 | + | Missense_Mutation | SNP | A | A | G | TCGA-A8-A07F-01A-11W-A019-09 | TCGA-A8-A07F-10A-01W-A021-09 | g.chr4:177071638A>G | c.2270A>G | c.(2269-2271)aAt>aGt | p.N757S |
| BRCA | 4 | 177071740 | 177071740 | + | Missense_Mutation | SNP | G | G | C | TCGA-A8-A07C-01A-11D-A045-09 | TCGA-A8-A07C-10A-01W-A055-09 | g.chr4:177071740G>C | c.2372G>C | c.(2371-2373)aGa>aCa | p.R791T |
| BRCA | 4 | 177072997 | 177072997 | + | Missense_Mutation | SNP | C | C | G | TCGA-E9-A1ND-01A-11D-A142-09 | TCGA-E9-A1ND-10A-01W-A187-09 | g.chr4:177072997C>G | c.2411C>G | c.(2410-2412)tCt>tGt | p.S804C |
| BRCA | 4 | 177083309 | 177083309 | + | Missense_Mutation | SNP | C | C | T | TCGA-E9-A3HO-01A-11D-A20S-09 | TCGA-E9-A3HO-10A-02D-A20S-09 | g.chr4:177083309C>T | c.2906C>T | c.(2905-2907)gCc>gTc | p.A969V |
| BRCA | 4 | 177095863 | 177095863 | + | Missense_Mutation | SNP | A | A | G | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr4:177095863A>G | c.3560A>G | c.(3559-3561)tAc>tGc | p.Y1187C |
| CESC | 4 | 177046324 | 177046324 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A0TN-01A-21D-A14W-08 | TCGA-C5-A0TN-10B-01D-A14W-08 | g.chr4:177046324C>T | c.680C>T | c.(679-681)aCg>aTg | p.T227M |
| CESC | 4 | 177046476 | 177046476 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr4:177046476C>T | c.832C>T | c.(832-834)Ccc>Tcc | p.P278S |
| CESC | 4 | 177046476 | 177046476 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A3HL-01A-11D-A20U-09 | TCGA-C5-A3HL-10A-01D-A20U-09 | g.chr4:177046476C>T | c.832C>T | c.(832-834)Ccc>Tcc | p.P278S |
| CESC | 4 | 177052785 | 177052785 | + | Missense_Mutation | SNP | C | C | G | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr4:177052785C>G | c.1066C>G | c.(1066-1068)Caa>Gaa | p.Q356E |
| CESC | 4 | 177058704 | 177058704 | + | Missense_Mutation | SNP | G | G | A | TCGA-JW-A69B-01A-11D-A32I-09 | TCGA-JW-A69B-10A-01D-A32I-09 | g.chr4:177058704G>A | c.1373G>A | c.(1372-1374)cGa>cAa | p.R458Q |
| CESC | 4 | 177082071 | 177082071 | + | Missense_Mutation | SNP | G | G | A | TCGA-IR-A3LA-01A-11D-A22X-09 | TCGA-IR-A3LA-10A-01D-A22X-09 | g.chr4:177082071G>A | c.2740G>A | c.(2740-2742)Gaa>Aaa | p.E914K |
| COAD | 4 | 177032829 | 177032829 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3554-01A-01W-0833-10 | TCGA-AA-3554-10A-01W-0833-10 | g.chr4:177032829C>T | c.170C>T | c.(169-171)gCg>gTg | p.A57V |
| COAD | 4 | 177032838 | 177032838 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3851-01A-01W-0995-10 | TCGA-AA-3851-10A-01W-0995-10 | g.chr4:177032838C>A | c.179C>A | c.(178-180)gCt>gAt | p.A60D |
| COAD | 4 | 177046287 | 177046287 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:177046287G>T | c.643G>T | c.(643-645)Gaa>Taa | p.E215* |
| COAD | 4 | 177046348 | 177046348 | + | Missense_Mutation | SNP | C | C | G | TCGA-CK-4947-01B-11D-1650-10 | TCGA-CK-4947-10A-01D-1650-10 | g.chr4:177046348C>G | c.704C>G | c.(703-705)tCt>tGt | p.S235C |
| COAD | 4 | 177046419 | 177046419 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr4:177046419A>G | c.775A>G | c.(775-777)Ata>Gta | p.I259V |
| COAD | 4 | 177046419 | 177046419 | + | Missense_Mutation | SNP | A | A | G | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr4:177046419A>G | c.775A>G | c.(775-777)Ata>Gta | p.I259V |
| COAD | 4 | 177046420 | 177046420 | + | Missense_Mutation | SNP | T | T | A | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr4:177046420T>A | c.776T>A | c.(775-777)aTa>aAa | p.I259K |
| COAD | 4 | 177046453 | 177046453 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr4:177046453C>A | c.809C>A | c.(808-810)tCt>tAt | p.S270Y |
| COAD | 4 | 177052795 | 177052795 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr4:177052795C>A | c.1076C>A | c.(1075-1077)tCt>tAt | p.S359Y |
| COAD | 4 | 177052822 | 177052822 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177052822G>A | c.1103G>A | c.(1102-1104)tGt>tAt | p.C368Y |
| COAD | 4 | 177058734 | 177058734 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6168-01A-11D-1650-10 | TCGA-CM-6168-10A-01D-1650-10 | g.chr4:177058734A>G | c.1403A>G | c.(1402-1404)aAg>aGg | p.K468R |
| COAD | 4 | 177067311 | 177067311 | + | Splice_Site | SNP | G | G | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr4:177067311G>A | | c.e13+1 | |
| COAD | 4 | 177069292 | 177069292 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr4:177069292G>A | c.1775G>A | c.(1774-1776)cGa>cAa | p.R592Q |
| COAD | 4 | 177071014 | 177071014 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177071014A>G | c.2026A>G | c.(2026-2028)Aca>Gca | p.T676A |
| COAD | 4 | 177071291 | 177071292 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr4:177071291_177071292insA | c.2217_2218insA | c.(2218-2220)aaafs | p.K740fs |
| COAD | 4 | 177071648 | 177071648 | + | Silent | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr4:177071648C>T | c.2280C>T | c.(2278-2280)aaC>aaT | p.N760N |
| COAD | 4 | 177072975 | 177072975 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177072975G>T | c.2389G>T | c.(2389-2391)Gaa>Taa | p.E797* |
| COAD | 4 | 177081145 | 177081145 | + | Splice_Site | SNP | G | G | A | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr4:177081145G>A | c.2598G>A | c.(2596-2598)agG>agA | p.R866R |
| COAD | 4 | 177081235 | 177081235 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177081235C>A | c.2688C>A | c.(2686-2688)ttC>ttA | p.F896L |
| COAD | 4 | 177081240 | 177081240 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr4:177081240C>T | c.2693C>T | c.(2692-2694)tCa>tTa | p.S898L |
| COAD | 4 | 177082100 | 177082100 | + | Silent | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr4:177082100C>T | c.2769C>T | c.(2767-2769)tcC>tcT | p.S923S |
| COAD | 4 | 177084326 | 177084326 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6920-01A-11D-1924-10 | TCGA-D5-6920-10A-01D-1924-10 | g.chr4:177084326C>T | c.2944C>T | c.(2944-2946)Cgc>Tgc | p.R982C |
| COAD | 4 | 177084327 | 177084327 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6606-01A-11D-1835-10 | TCGA-AZ-6606-11A-01D-1835-10 | g.chr4:177084327G>A | c.2945G>A | c.(2944-2946)cGc>cAc | p.R982H |
| COAD | 4 | 177084384 | 177084384 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6922-01A-11D-1924-10 | TCGA-D5-6922-10A-01D-1924-10 | g.chr4:177084384C>T | c.3002C>T | c.(3001-3003)gCa>gTa | p.A1001V |
| COAD | 4 | 177089878 | 177089878 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr4:177089878A>C | c.3163A>C | c.(3163-3165)Aaa>Caa | p.K1055Q |
| COAD | 4 | 177093625 | 177093625 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:177093625G>T | c.3319G>T | c.(3319-3321)Gaa>Taa | p.E1107* |
| COAD | 4 | 177093636 | 177093636 | + | Silent | SNP | A | A | G | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr4:177093636A>G | c.3330A>G | c.(3328-3330)aaA>aaG | p.K1110K |
| COAD | 4 | 177093644 | 177093644 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr4:177093644C>A | c.3338C>A | c.(3337-3339)cCt>cAt | p.P1113H |
| COAD | 4 | 177094469 | 177094469 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr4:177094469A>G | c.3413A>G | c.(3412-3414)gAc>gGc | p.D1138G |
| COAD | 4 | 177098258 | 177098258 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177098258C>A | c.3616C>A | c.(3616-3618)Ctt>Att | p.L1206I |
| COAD | 4 | 177098780 | 177098780 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr4:177098780C>A | c.3824C>A | c.(3823-3825)tCt>tAt | p.S1275Y |
| COAD | 4 | 177098789 | 177098789 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr4:177098789C>T | c.3833C>T | c.(3832-3834)aCg>aTg | p.T1278M |
| COAD | 4 | 177100691 | 177100691 | + | Silent | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:177100691C>T | c.3930C>T | c.(3928-3930)ttC>ttT | p.F1310F |
| COADREAD | 4 | 177032829 | 177032829 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3554-01A-01W-0833-10 | TCGA-AA-3554-10A-01W-0833-10 | g.chr4:177032829C>T | c.170C>T | c.(169-171)gCg>gTg | p.A57V |
| COADREAD | 4 | 177032838 | 177032838 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3851-01A-01W-0995-10 | TCGA-AA-3851-10A-01W-0995-10 | g.chr4:177032838C>A | c.179C>A | c.(178-180)gCt>gAt | p.A60D |
| COADREAD | 4 | 177046287 | 177046287 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:177046287G>T | c.643G>T | c.(643-645)Gaa>Taa | p.E215* |
| COADREAD | 4 | 177046348 | 177046348 | + | Missense_Mutation | SNP | C | C | G | TCGA-CK-4947-01B-11D-1650-10 | TCGA-CK-4947-10A-01D-1650-10 | g.chr4:177046348C>G | c.704C>G | c.(703-705)tCt>tGt | p.S235C |
| COADREAD | 4 | 177046419 | 177046419 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr4:177046419A>G | c.775A>G | c.(775-777)Ata>Gta | p.I259V |
| COADREAD | 4 | 177046419 | 177046419 | + | Missense_Mutation | SNP | A | A | G | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr4:177046419A>G | c.775A>G | c.(775-777)Ata>Gta | p.I259V |
| COADREAD | 4 | 177046420 | 177046420 | + | Missense_Mutation | SNP | T | T | A | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr4:177046420T>A | c.776T>A | c.(775-777)aTa>aAa | p.I259K |
| COADREAD | 4 | 177046453 | 177046453 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr4:177046453C>A | c.809C>A | c.(808-810)tCt>tAt | p.S270Y |
| COADREAD | 4 | 177049909 | 177049909 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:177049909C>T | c.883C>T | c.(883-885)Cgc>Tgc | p.R295C |
| COADREAD | 4 | 177049909 | 177049909 | + | Missense_Mutation | SNP | C | C | T | TCGA-DY-A0XA-01A-11D-A152-10 | TCGA-DY-A0XA-10A-01D-A152-10 | g.chr4:177049909C>T | c.883C>T | c.(883-885)Cgc>Tgc | p.R295C |
| COADREAD | 4 | 177052795 | 177052795 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr4:177052795C>A | c.1076C>A | c.(1075-1077)tCt>tAt | p.S359Y |
| COADREAD | 4 | 177052822 | 177052822 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177052822G>A | c.1103G>A | c.(1102-1104)tGt>tAt | p.C368Y |
| COADREAD | 4 | 177058734 | 177058734 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6168-01A-11D-1650-10 | TCGA-CM-6168-10A-01D-1650-10 | g.chr4:177058734A>G | c.1403A>G | c.(1402-1404)aAg>aGg | p.K468R |
| COADREAD | 4 | 177067311 | 177067311 | + | Splice_Site | SNP | G | G | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr4:177067311G>A | | c.e13+1 | |
| COADREAD | 4 | 177069292 | 177069292 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr4:177069292G>A | c.1775G>A | c.(1774-1776)cGa>cAa | p.R592Q |
| COADREAD | 4 | 177069341 | 177069341 | + | Silent | SNP | C | C | T | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr4:177069341C>T | c.1824C>T | c.(1822-1824)caC>caT | p.H608H |
| COADREAD | 4 | 177071014 | 177071014 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177071014A>G | c.2026A>G | c.(2026-2028)Aca>Gca | p.T676A |
| COADREAD | 4 | 177071291 | 177071292 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr4:177071291_177071292insA | c.2217_2218insA | c.(2218-2220)aaafs | p.K740fs |
| COADREAD | 4 | 177071648 | 177071648 | + | Silent | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr4:177071648C>T | c.2280C>T | c.(2278-2280)aaC>aaT | p.N760N |
| COADREAD | 4 | 177072975 | 177072975 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177072975G>T | c.2389G>T | c.(2389-2391)Gaa>Taa | p.E797* |
| COADREAD | 4 | 177081145 | 177081145 | + | Splice_Site | SNP | G | G | A | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr4:177081145G>A | c.2598G>A | c.(2596-2598)agG>agA | p.R866R |
| COADREAD | 4 | 177081235 | 177081235 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177081235C>A | c.2688C>A | c.(2686-2688)ttC>ttA | p.F896L |
| COADREAD | 4 | 177081240 | 177081240 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr4:177081240C>T | c.2693C>T | c.(2692-2694)tCa>tTa | p.S898L |
| COADREAD | 4 | 177082100 | 177082100 | + | Silent | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr4:177082100C>T | c.2769C>T | c.(2767-2769)tcC>tcT | p.S923S |
| COADREAD | 4 | 177084326 | 177084326 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6920-01A-11D-1924-10 | TCGA-D5-6920-10A-01D-1924-10 | g.chr4:177084326C>T | c.2944C>T | c.(2944-2946)Cgc>Tgc | p.R982C |
| COADREAD | 4 | 177084327 | 177084327 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6606-01A-11D-1835-10 | TCGA-AZ-6606-11A-01D-1835-10 | g.chr4:177084327G>A | c.2945G>A | c.(2944-2946)cGc>cAc | p.R982H |
| COADREAD | 4 | 177084384 | 177084384 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6922-01A-11D-1924-10 | TCGA-D5-6922-10A-01D-1924-10 | g.chr4:177084384C>T | c.3002C>T | c.(3001-3003)gCa>gTa | p.A1001V |
| COADREAD | 4 | 177089878 | 177089878 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr4:177089878A>C | c.3163A>C | c.(3163-3165)Aaa>Caa | p.K1055Q |
| COADREAD | 4 | 177093609 | 177093609 | + | Nonsense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:177093609T>G | c.3303T>G | c.(3301-3303)taT>taG | p.Y1101* |
| COADREAD | 4 | 177093625 | 177093625 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:177093625G>T | c.3319G>T | c.(3319-3321)Gaa>Taa | p.E1107* |
| COADREAD | 4 | 177093636 | 177093636 | + | Silent | SNP | A | A | G | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr4:177093636A>G | c.3330A>G | c.(3328-3330)aaA>aaG | p.K1110K |
| COADREAD | 4 | 177093644 | 177093644 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr4:177093644C>A | c.3338C>A | c.(3337-3339)cCt>cAt | p.P1113H |
| COADREAD | 4 | 177094469 | 177094469 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr4:177094469A>G | c.3413A>G | c.(3412-3414)gAc>gGc | p.D1138G |
| COADREAD | 4 | 177098225 | 177098225 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:177098225C>T | c.3583C>T | c.(3583-3585)Cgg>Tgg | p.R1195W |
| COADREAD | 4 | 177098258 | 177098258 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:177098258C>A | c.3616C>A | c.(3616-3618)Ctt>Att | p.L1206I |
| COADREAD | 4 | 177098286 | 177098286 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:177098286C>T | c.3644C>T | c.(3643-3645)gCt>gTt | p.A1215V |
| COADREAD | 4 | 177098780 | 177098780 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr4:177098780C>A | c.3824C>A | c.(3823-3825)tCt>tAt | p.S1275Y |
| COADREAD | 4 | 177098789 | 177098789 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr4:177098789C>T | c.3833C>T | c.(3832-3834)aCg>aTg | p.T1278M |
| COADREAD | 4 | 177100635 | 177100635 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-4007-01A-01W-1073-09 | TCGA-AG-4007-10A-01W-1073-09 | g.chr4:177100635G>A | c.3874G>A | c.(3874-3876)Ggg>Agg | p.G1292R |
| COADREAD | 4 | 177100691 | 177100691 | + | Silent | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:177100691C>T | c.3930C>T | c.(3928-3930)ttC>ttT | p.F1310F |
| DLBC | 4 | 177089839 | 177089839 | + | Missense_Mutation | SNP | C | C | G | TCGA-G8-6906-01A-11D-2210-10 | TCGA-G8-6906-14A-01D-2210-10 | g.chr4:177089839C>G | c.3124C>G | c.(3124-3126)Ctt>Gtt | p.L1042V |
| ESCA | 4 | 177037078 | 177037078 | + | Silent | SNP | C | C | A | TCGA-L5-A891-01A-11D-A36J-09 | TCGA-L5-A891-11A-21D-A36M-09 | g.chr4:177037078C>A | c.327C>A | c.(325-327)atC>atA | p.I109I |
| ESCA | 4 | 177041086 | 177041086 | + | Missense_Mutation | SNP | C | C | T | TCGA-IG-A50L-01A-11D-A27G-09 | TCGA-IG-A50L-10A-01D-A27G-09 | g.chr4:177041086C>T | c.448C>T | c.(448-450)Cca>Tca | p.P150S |
| ESCA | 4 | 177046415 | 177046415 | + | Silent | SNP | T | T | C | TCGA-IG-A4QS-01A-11D-A27G-09 | TCGA-IG-A4QS-10A-01D-A27G-09 | g.chr4:177046415T>C | c.771T>C | c.(769-771)tcT>tcC | p.S257S |
| ESCA | 4 | 177052812 | 177052812 | + | Missense_Mutation | SNP | G | G | A | TCGA-JY-A93F-01A-21D-A37C-09 | TCGA-JY-A93F-10A-01D-A37F-09 | g.chr4:177052812G>A | c.1093G>A | c.(1093-1095)Gca>Aca | p.A365T |
| ESCA | 4 | 177052846 | 177052846 | + | Missense_Mutation | SNP | T | T | G | TCGA-IG-A4QS-01A-11D-A27G-09 | TCGA-IG-A4QS-10A-01D-A27G-09 | g.chr4:177052846T>G | c.1127T>G | c.(1126-1128)cTt>cGt | p.L376R |
| ESCA | 4 | 177052858 | 177052858 | + | Missense_Mutation | SNP | G | G | C | TCGA-IG-A4P3-01A-11D-A27G-09 | TCGA-IG-A4P3-10A-01D-A27G-09 | g.chr4:177052858G>C | c.1139G>C | c.(1138-1140)gGa>gCa | p.G380A |
| ESCA | 4 | 177056320 | 177056320 | + | Missense_Mutation | SNP | C | C | A | TCGA-RE-A7BO-01A-11D-A33E-09 | TCGA-RE-A7BO-10A-01D-A33H-09 | g.chr4:177056320C>A | c.1232C>A | c.(1231-1233)aCa>aAa | p.T411K |
| ESCA | 4 | 177058691 | 177058691 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr4:177058691delG | c.1360delG | c.(1360-1362)gggfs | p.G455fs |
| ESCA | 4 | 177061048 | 177061048 | + | Silent | SNP | A | A | T | TCGA-L5-A8NU-01A-11D-A36J-09 | TCGA-L5-A8NU-11A-11D-A36M-09 | g.chr4:177061048A>T | c.1437A>T | c.(1435-1437)ggA>ggT | p.G479G |
| ESCA | 4 | 177067295 | 177067295 | + | Missense_Mutation | SNP | G | G | T | TCGA-KH-A6WC-01A-11D-A33E-09 | TCGA-KH-A6WC-10B-01D-A33H-09 | g.chr4:177067295G>T | c.1751G>T | c.(1750-1752)aGt>aTt | p.S584I |
| ESCA | 4 | 177071685 | 177071685 | + | Missense_Mutation | SNP | C | C | T | TCGA-R6-A6Y0-01B-11D-A33E-09 | TCGA-R6-A6Y0-10A-01D-A33H-09 | g.chr4:177071685C>T | c.2317C>T | c.(2317-2319)Ctt>Ttt | p.L773F |
| ESCA | 4 | 177072975 | 177072975 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-R6-A6XQ-01B-11D-A33E-09 | TCGA-R6-A6XQ-10A-01D-A33H-09 | g.chr4:177072975G>T | c.2389G>T | c.(2389-2391)Gaa>Taa | p.E797* |
| ESCA | 4 | 177094439 | 177094439 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OH-01A-11D-A27G-09 | TCGA-L5-A4OH-11A-11D-A27G-09 | g.chr4:177094439G>T | c.3383G>T | c.(3382-3384)tGg>tTg | p.W1128L |
| ESCA | 4 | 177094487 | 177094487 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4ON-01A-11D-A27G-09 | TCGA-L5-A4ON-11A-21D-A27G-09 | g.chr4:177094487G>T | c.3431G>T | c.(3430-3432)cGt>cTt | p.R1144L |
| ESCA | 4 | 177095823 | 177095823 | + | Missense_Mutation | SNP | A | A | G | TCGA-2H-A9GI-01A-11D-A37C-09 | TCGA-2H-A9GI-11A-11D-A37F-09 | g.chr4:177095823A>G | c.3520A>G | c.(3520-3522)Aga>Gga | p.R1174G |
| ESCA | 4 | 177098797 | 177098797 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-R6-A6L4-01A-11D-A31U-09 | TCGA-R6-A6L4-10A-01D-A31U-09 | g.chr4:177098797A>T | c.3841A>T | c.(3841-3843)Aaa>Taa | p.K1281* |
| GBMLGG | 4 | 177032847 | 177032847 | + | Missense_Mutation | SNP | T | T | C | TCGA-DH-A66B-01A-11D-A29Q-08 | TCGA-DH-A66B-10A-01D-A29Q-08 | g.chr4:177032847T>C | c.188T>C | c.(187-189)aTt>aCt | p.I63T |
| GBMLGG | 4 | 177052789 | 177052789 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:177052789C>T | c.1070C>T | c.(1069-1071)gCa>gTa | p.A357V |
| GBMLGG | 4 | 177067236 | 177067236 | + | Silent | SNP | G | G | A | TCGA-S9-A6WL-01A-21D-A33T-08 | TCGA-S9-A6WL-10A-01D-A33W-08 | g.chr4:177067236G>A | c.1692G>A | c.(1690-1692)ggG>ggA | p.G564G |
| GBMLGG | 4 | 177094487 | 177094487 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:177094487G>A | c.3431G>A | c.(3430-3432)cGt>cAt | p.R1144H |
| HNSC | 4 | 177032852 | 177032852 | + | Missense_Mutation | SNP | C | C | A | TCGA-D6-8569-01A-11D-2394-08 | TCGA-D6-8569-10A-01D-2394-08 | g.chr4:177032852C>A | c.193C>A | c.(193-195)Cag>Aag | p.Q65K |
| HNSC | 4 | 177041154 | 177041154 | + | Silent | SNP | C | C | T | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr4:177041154C>T | c.516C>T | c.(514-516)ttC>ttT | p.F172F |
| HNSC | 4 | 177041161 | 177041161 | + | Missense_Mutation | SNP | G | G | T | TCGA-CR-5248-01A-01D-2012-08 | TCGA-CR-5248-10A-01D-2013-08 | g.chr4:177041161G>T | c.523G>T | c.(523-525)Gat>Tat | p.D175Y |
| HNSC | 4 | 177046431 | 177046431 | + | Missense_Mutation | SNP | A | A | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr4:177046431A>T | c.787A>T | c.(787-789)Aat>Tat | p.N263Y |
| HNSC | 4 | 177052705 | 177052705 | + | Splice_Site | SNP | T | T | C | TCGA-P3-A6T8-01A-11D-A34J-08 | TCGA-P3-A6T8-10A-01D-A34M-08 | g.chr4:177052705T>C | c.986T>C | c.(985-987)tTt>tCt | p.F329S |
| HNSC | 4 | 177052728 | 177052728 | + | Missense_Mutation | SNP | A | A | C | TCGA-D6-A74Q-01A-11D-A34J-08 | TCGA-D6-A74Q-10A-02D-A34M-08 | g.chr4:177052728A>C | c.1009A>C | c.(1009-1011)Aat>Cat | p.N337H |
| HNSC | 4 | 177052768 | 177052768 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-5356-01A-01D-1434-08 | TCGA-CN-5356-10A-01D-1434-08 | g.chr4:177052768C>T | c.1049C>T | c.(1048-1050)cCa>cTa | p.P350L |
| HNSC | 4 | 177056261 | 177056261 | + | Silent | SNP | A | A | T | TCGA-BA-A6DA-01A-31D-A31L-08 | TCGA-BA-A6DA-10A-01D-A31J-08 | g.chr4:177056261A>T | c.1173A>T | c.(1171-1173)ggA>ggT | p.G391G |
| HNSC | 4 | 177056354 | 177056354 | + | Silent | SNP | T | T | C | TCGA-CR-7364-01A-11D-2012-08 | TCGA-CR-7364-10A-01D-2013-08 | g.chr4:177056354T>C | c.1266T>C | c.(1264-1266)gaT>gaC | p.D422D |
| HNSC | 4 | 177067180 | 177067180 | + | Missense_Mutation | SNP | G | G | C | TCGA-F7-A50J-01A-21D-A28R-08 | TCGA-F7-A50J-10A-01D-A28U-08 | g.chr4:177067180G>C | c.1636G>C | c.(1636-1638)Gtt>Ctt | p.V546L |
| HNSC | 4 | 177067239 | 177067239 | + | Silent | SNP | T | T | C | TCGA-BA-4074-01A-01D-1434-08 | TCGA-BA-4074-10A-01D-1434-08 | g.chr4:177067239T>C | c.1695T>C | c.(1693-1695)caT>caC | p.H565H |
| HNSC | 4 | 177071078 | 177071078 | + | Missense_Mutation | SNP | G | G | C | TCGA-CQ-6218-01A-11D-1912-08 | TCGA-CQ-6218-10A-01D-1912-08 | g.chr4:177071078G>C | c.2090G>C | c.(2089-2091)aGa>aCa | p.R697T |
| HNSC | 4 | 177071209 | 177071209 | + | Missense_Mutation | SNP | C | C | A | TCGA-D6-A74Q-01A-11D-A34J-08 | TCGA-D6-A74Q-10A-02D-A34M-08 | g.chr4:177071209C>A | c.2135C>A | c.(2134-2136)cCa>cAa | p.P712Q |
| HNSC | 4 | 177071267 | 177071267 | + | Silent | SNP | A | A | G | TCGA-CV-5978-01A-11D-1683-08 | TCGA-CV-5978-11A-01D-1683-08 | g.chr4:177071267A>G | c.2193A>G | c.(2191-2193)gaA>gaG | p.E731E |
| HNSC | 4 | 177071286 | 177071286 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-QK-AA3J-01A-11D-A391-08 | TCGA-QK-AA3J-10A-01D-A394-08 | g.chr4:177071286C>T | c.2212C>T | c.(2212-2214)Caa>Taa | p.Q738* |
| HNSC | 4 | 177071305 | 177071305 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-A461-01A-41D-A25Y-08 | TCGA-CV-A461-10A-01D-A25Y-08 | g.chr4:177071305G>T | c.2231G>T | c.(2230-2232)tGg>tTg | p.W744L |
| HNSC | 4 | 177077229 | 177077229 | + | Splice_Site | SNP | G | G | T | TCGA-CV-6956-01A-21D-2012-08 | TCGA-CV-6956-10A-01D-2013-08 | g.chr4:177077229G>T | | c.e19-1 | |
| HNSC | 4 | 177077242 | 177077242 | + | Silent | SNP | C | C | T | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr4:177077242C>T | c.2545C>T | c.(2545-2547)Ctg>Ttg | p.L849L |
| HNSC | 4 | 177081214 | 177081214 | + | Silent | SNP | G | G | A | TCGA-CR-7379-01A-11D-2012-08 | TCGA-CR-7379-10A-01D-2013-08 | g.chr4:177081214G>A | c.2667G>A | c.(2665-2667)gtG>gtA | p.V889V |
| HNSC | 4 | 177084311 | 177084311 | + | Missense_Mutation | SNP | A | A | G | TCGA-BA-A6DL-01A-21D-A30E-08 | TCGA-BA-A6DL-10A-01D-A30H-08 | g.chr4:177084311A>G | c.2929A>G | c.(2929-2931)Atg>Gtg | p.M977V |
| HNSC | 4 | 177084360 | 177084360 | + | Missense_Mutation | SNP | G | G | C | TCGA-KU-A6H7-01A-11D-A31L-08 | TCGA-KU-A6H7-10A-01D-A31J-08 | g.chr4:177084360G>C | c.2978G>C | c.(2977-2979)gGc>gCc | p.G993A |
| HNSC | 4 | 177084375 | 177084375 | + | Missense_Mutation | SNP | A | A | T | TCGA-CR-7364-01A-11D-2012-08 | TCGA-CR-7364-10A-01D-2013-08 | g.chr4:177084375A>T | c.2993A>T | c.(2992-2994)gAg>gTg | p.E998V |
| HNSC | 4 | 177089908 | 177089908 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr4:177089908G>A | c.3193G>A | c.(3193-3195)Gaa>Aaa | p.E1065K |
| HNSC | 4 | 177094455 | 177094455 | + | Missense_Mutation | SNP | A | A | G | TCGA-CV-A461-01A-41D-A25Y-08 | TCGA-CV-A461-10A-01D-A25Y-08 | g.chr4:177094455A>G | c.3399A>G | c.(3397-3399)atA>atG | p.I1133M |
| HNSC | 4 | 177094477 | 177094477 | + | Missense_Mutation | SNP | A | A | T | TCGA-BA-A6DA-01A-31D-A31L-08 | TCGA-BA-A6DA-10A-01D-A31J-08 | g.chr4:177094477A>T | c.3421A>T | c.(3421-3423)Agc>Tgc | p.S1141C |
| HNSC | 4 | 177098210 | 177098210 | + | Splice_Site | SNP | C | C | A | TCGA-CR-7399-01A-11D-2012-08 | TCGA-CR-7399-10A-01D-2013-08 | g.chr4:177098210C>A | c.3568C>A | c.(3568-3570)Cag>Aag | p.Q1190K |
| HNSC | 4 | 177098223 | 177098223 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-A63U-01A-11D-A30E-08 | TCGA-CN-A63U-10A-01D-A30H-08 | g.chr4:177098223G>T | c.3581G>T | c.(3580-3582)cGt>cTt | p.R1194L |
| HNSC | 4 | 177098636 | 177098636 | + | Missense_Mutation | SNP | C | C | A | TCGA-CN-5356-01A-01D-1434-08 | TCGA-CN-5356-10A-01D-1434-08 | g.chr4:177098636C>A | c.3680C>A | c.(3679-3681)tCt>tAt | p.S1227Y |
| KIPAN | 4 | 177050013 | 177050013 | + | Splice_Site | SNP | T | T | C | TCGA-B4-5836-01A-11D-1669-08 | TCGA-B4-5836-10A-01D-1669-08 | g.chr4:177050013T>C | | c.e7+2 | |
| KIPAN | 4 | 177056301 | 177056301 | + | Missense_Mutation | SNP | G | G | A | TCGA-HE-A5NL-01A-11D-A26P-10 | TCGA-HE-A5NL-10A-01D-A26P-10 | g.chr4:177056301G>A | c.1213G>A | c.(1213-1215)Gat>Aat | p.D405N |
| KIPAN | 4 | 177084327 | 177084327 | + | Missense_Mutation | SNP | G | G | A | TCGA-B8-5553-01A-01D-1534-10 | TCGA-B8-5553-10A-01D-1535-10 | g.chr4:177084327G>A | c.2945G>A | c.(2944-2946)cGc>cAc | p.R982H |
| KIPAN | 4 | 177089815 | 177089815 | + | Missense_Mutation | SNP | G | G | C | TCGA-MH-A55Z-01A-11D-A26P-10 | TCGA-MH-A55Z-10A-01D-A26P-10 | g.chr4:177089815G>C | c.3100G>C | c.(3100-3102)Gtt>Ctt | p.V1034L |
| KIPAN | 4 | 177094493 | 177094493 | + | Missense_Mutation | SNP | A | A | T | TCGA-CJ-4875-01A-01D-1373-10 | TCGA-CJ-4875-11A-01D-1373-10 | g.chr4:177094493A>T | c.3437A>T | c.(3436-3438)gAa>gTa | p.E1146V |
| KIPAN | 4 | 177098210 | 177098210 | + | Splice_Site | SNP | C | C | A | TCGA-5P-A9JW-01A-11D-A42J-10 | TCGA-5P-A9JW-10A-01D-A42M-10 | g.chr4:177098210C>A | c.3568C>A | c.(3568-3570)Cag>Aag | p.Q1190K |
| KIPAN | 4 | 177098622 | 177098622 | + | Splice_Site | SNP | A | A | G | TCGA-SX-A71S-01A-11D-A33Q-10 | TCGA-SX-A71S-10A-01D-A33Q-10 | g.chr4:177098622A>G | c.3666A>G | c.(3664-3666)agA>agG | p.R1222R |
| KIRC | 4 | 177050013 | 177050013 | + | Splice_Site | SNP | T | T | C | TCGA-B4-5836-01A-11D-1669-08 | TCGA-B4-5836-10A-01D-1669-08 | g.chr4:177050013T>C | | c.e7+2 | |
| KIRC | 4 | 177084327 | 177084327 | + | Missense_Mutation | SNP | G | G | A | TCGA-B8-5553-01A-01D-1534-10 | TCGA-B8-5553-10A-01D-1535-10 | g.chr4:177084327G>A | c.2945G>A | c.(2944-2946)cGc>cAc | p.R982H |
| KIRC | 4 | 177094493 | 177094493 | + | Missense_Mutation | SNP | A | A | T | TCGA-CJ-4875-01A-01D-1373-10 | TCGA-CJ-4875-11A-01D-1373-10 | g.chr4:177094493A>T | c.3437A>T | c.(3436-3438)gAa>gTa | p.E1146V |
| KIRP | 4 | 177056301 | 177056301 | + | Missense_Mutation | SNP | G | G | A | TCGA-HE-A5NL-01A-11D-A26P-10 | TCGA-HE-A5NL-10A-01D-A26P-10 | g.chr4:177056301G>A | c.1213G>A | c.(1213-1215)Gat>Aat | p.D405N |
| KIRP | 4 | 177089815 | 177089815 | + | Missense_Mutation | SNP | G | G | C | TCGA-MH-A55Z-01A-11D-A26P-10 | TCGA-MH-A55Z-10A-01D-A26P-10 | g.chr4:177089815G>C | c.3100G>C | c.(3100-3102)Gtt>Ctt | p.V1034L |
| KIRP | 4 | 177098210 | 177098210 | + | Splice_Site | SNP | C | C | A | TCGA-5P-A9JW-01A-11D-A42J-10 | TCGA-5P-A9JW-10A-01D-A42M-10 | g.chr4:177098210C>A | c.3568C>A | c.(3568-3570)Cag>Aag | p.Q1190K |
| KIRP | 4 | 177098622 | 177098622 | + | Splice_Site | SNP | A | A | G | TCGA-SX-A71S-01A-11D-A33Q-10 | TCGA-SX-A71S-10A-01D-A33Q-10 | g.chr4:177098622A>G | c.3666A>G | c.(3664-3666)agA>agG | p.R1222R |
| LGG | 4 | 177032847 | 177032847 | + | Missense_Mutation | SNP | T | T | C | TCGA-DH-A66B-01A-11D-A29Q-08 | TCGA-DH-A66B-10A-01D-A29Q-08 | g.chr4:177032847T>C | c.188T>C | c.(187-189)aTt>aCt | p.I63T |
| LGG | 4 | 177052789 | 177052789 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:177052789C>T | c.1070C>T | c.(1069-1071)gCa>gTa | p.A357V |
| LGG | 4 | 177067236 | 177067236 | + | Silent | SNP | G | G | A | TCGA-S9-A6WL-01A-21D-A33T-08 | TCGA-S9-A6WL-10A-01D-A33W-08 | g.chr4:177067236G>A | c.1692G>A | c.(1690-1692)ggG>ggA | p.G564G |
| LGG | 4 | 177094487 | 177094487 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:177094487G>A | c.3431G>A | c.(3430-3432)cGt>cAt | p.R1144H |
| LIHC | 4 | 177041041 | 177041041 | + | Missense_Mutation | SNP | T | T | C | TCGA-ED-A7XO-01A-11D-A34Z-10 | TCGA-ED-A7XO-10A-01D-A34Z-10 | g.chr4:177041041T>C | c.403T>C | c.(403-405)Tgc>Cgc | p.C135R |
| LIHC | 4 | 177052791 | 177052791 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr4:177052791delT | c.1072delT | c.(1072-1074)tttfs | p.F358fs |
| LIHC | 4 | 177056301 | 177056301 | + | Missense_Mutation | SNP | G | G | A | TCGA-DD-AADU-01A-11D-A40R-10 | TCGA-DD-AADU-10A-01D-A40U-10 | g.chr4:177056301G>A | c.1213G>A | c.(1213-1215)Gat>Aat | p.D405N |
| LIHC | 4 | 177058704 | 177058704 | + | Missense_Mutation | SNP | G | G | A | TCGA-DD-A4NN-01A-11D-A28X-10 | TCGA-DD-A4NN-10A-01D-A28X-10 | g.chr4:177058704G>A | c.1373G>A | c.(1372-1374)cGa>cAa | p.R458Q |
| LIHC | 4 | 177067183 | 177067183 | + | Missense_Mutation | SNP | C | C | T | TCGA-G3-A5SL-01A-11D-A27I-10 | TCGA-G3-A5SL-10A-01D-A27I-10 | g.chr4:177067183C>T | c.1639C>T | c.(1639-1641)Cgt>Tgt | p.R547C |
| LIHC | 4 | 177071048 | 177071048 | + | Missense_Mutation | SNP | C | C | A | TCGA-RC-A7SK-01A-11D-A34Z-10 | TCGA-RC-A7SK-10A-01D-A34Z-10 | g.chr4:177071048C>A | c.2060C>A | c.(2059-2061)aCt>aAt | p.T687N |
| LIHC | 4 | 177093632 | 177093632 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chr4:177093632delA | c.3326delA | c.(3325-3327)gaafs | p.E1109fs |
| LIHC | 4 | 177098697 | 177098697 | + | Silent | SNP | A | A | G | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr4:177098697A>G | c.3741A>G | c.(3739-3741)ctA>ctG | p.L1247L |
| LUAD | 4 | 177017722 | 177017722 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z020-01A-01W-0746-08 | TCGA-17-Z020-11A-01W-0746-08 | g.chr4:177017722G>C | c.52G>C | c.(52-54)Gaa>Caa | p.E18Q |
| LUAD | 4 | 177032808 | 177032808 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr4:177032808G>T | c.149G>T | c.(148-150)gGa>gTa | p.G50V |
| LUAD | 4 | 177041039 | 177041039 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-17-Z014-01A-01W-0746-08 | TCGA-17-Z014-11A-01W-0746-08 | g.chr4:177041039G>A | c.401G>A | c.(400-402)tGg>tAg | p.W134* |
| LUAD | 4 | 177041116 | 177041116 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-8585-01A-11D-2393-08 | TCGA-86-8585-10A-01D-2393-08 | g.chr4:177041116G>C | c.478G>C | c.(478-480)Gat>Cat | p.D160H |
| LUAD | 4 | 177046336 | 177046336 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-44-8119-01A-11D-2238-08 | TCGA-44-8119-10A-01D-2238-08 | g.chr4:177046336delG | c.692delG | c.(691-693)tggfs | p.W231fs |
| LUAD | 4 | 177049931 | 177049931 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8089-01A-11D-2238-08 | TCGA-55-8089-10A-01D-2238-08 | g.chr4:177049931C>T | c.905C>T | c.(904-906)aCa>aTa | p.T302I |
| LUAD | 4 | 177056385 | 177056385 | + | Missense_Mutation | SNP | C | C | T | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chr4:177056385C>T | c.1297C>T | c.(1297-1299)Ccg>Tcg | p.P433S |
| LUAD | 4 | 177058693 | 177058693 | + | Silent | SNP | G | G | T | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr4:177058693G>T | c.1362G>T | c.(1360-1362)ggG>ggT | p.G454G |
| LUAD | 4 | 177061070 | 177061070 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z044-01A-01W-0746-08 | TCGA-17-Z044-11A-01W-0746-08 | g.chr4:177061070G>C | c.1459G>C | c.(1459-1461)Gcc>Ccc | p.A487P |
| LUAD | 4 | 177061073 | 177061073 | + | Missense_Mutation | SNP | T | T | A | TCGA-50-6593-01A-11D-1753-08 | TCGA-50-6593-11A-01D-1753-08 | g.chr4:177061073T>A | c.1462T>A | c.(1462-1464)Tgg>Agg | p.W488R |
| LUAD | 4 | 177063217 | 177063217 | + | Missense_Mutation | SNP | A | A | G | TCGA-50-6594-01A-11D-1753-08 | TCGA-50-6594-11A-01D-1753-08 | g.chr4:177063217A>G | c.1598A>G | c.(1597-1599)aAt>aGt | p.N533S |
| LUAD | 4 | 177067163 | 177067163 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-7570-01A-11D-2036-08 | TCGA-55-7570-10A-01D-2036-08 | g.chr4:177067163G>T | c.1619G>T | c.(1618-1620)gGc>gTc | p.G540V |
| LUAD | 4 | 177067216 | 177067216 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr4:177067216C>A | c.1672C>A | c.(1672-1674)Cca>Aca | p.P558T |
| LUAD | 4 | 177069351 | 177069351 | + | Missense_Mutation | SNP | G | G | T | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr4:177069351G>T | c.1834G>T | c.(1834-1836)Gtg>Ttg | p.V612L |
| LUAD | 4 | 177069408 | 177069408 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z062-01A-01W-0747-08 | TCGA-17-Z062-11A-01W-0747-08 | g.chr4:177069408G>T | c.1891G>T | c.(1891-1893)Gac>Tac | p.D631Y |
| LUAD | 4 | 177069477 | 177069477 | + | Missense_Mutation | SNP | G | G | T | TCGA-64-1676-01A-01D-0969-08 | TCGA-64-1676-10A-01D-0969-08 | g.chr4:177069477G>T | c.1960G>T | c.(1960-1962)Gat>Tat | p.D654Y |
| LUAD | 4 | 177069485 | 177069485 | + | Splice_Site | SNP | T | T | C | TCGA-49-4506-01A-01D-1265-08 | TCGA-49-4506-11A-01D-1265-08 | g.chr4:177069485T>C | c.1968T>C | c.(1966-1968)taT>taC | p.Y656Y |
| LUAD | 4 | 177070978 | 177070978 | + | Missense_Mutation | SNP | C | C | A | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr4:177070978C>A | c.1990C>A | c.(1990-1992)Cgc>Agc | p.R664S |
| LUAD | 4 | 177071008 | 177071008 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z052-01A-01W-0747-08 | TCGA-17-Z052-11A-01W-0747-08 | g.chr4:177071008G>T | c.2020G>T | c.(2020-2022)Gac>Tac | p.D674Y |
| LUAD | 4 | 177071009 | 177071009 | + | Missense_Mutation | SNP | A | A | T | TCGA-17-Z023-01A-01W-0746-08 | TCGA-17-Z023-11A-01W-0746-08 | g.chr4:177071009A>T | c.2021A>T | c.(2020-2022)gAc>gTc | p.D674V |
| LUAD | 4 | 177071727 | 177071727 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-7980-01A-11D-2184-08 | TCGA-69-7980-10A-01D-2184-08 | g.chr4:177071727C>A | c.2359C>A | c.(2359-2361)Ctg>Atg | p.L787M |
| LUAD | 4 | 177073085 | 177073085 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr4:177073085G>T | c.2499G>T | c.(2497-2499)caG>caT | p.Q833H |
| LUAD | 4 | 177077246 | 177077246 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-44-5643-01A-01D-1625-08 | TCGA-44-5643-10A-01D-1625-08 | g.chr4:177077246C>A | c.2549C>A | c.(2548-2550)tCa>tAa | p.S850* |
| LUAD | 4 | 177083284 | 177083284 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr4:177083284G>T | c.2881G>T | c.(2881-2883)Gta>Tta | p.V961L |
| LUAD | 4 | 177083325 | 177083325 | + | Splice_Site | SNP | G | G | T | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr4:177083325G>T | c.2922G>T | c.(2920-2922)gaG>gaT | p.E974D |
| LUAD | 4 | 177093569 | 177093569 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr4:177093569C>T | c.3263C>T | c.(3262-3264)aCa>aTa | p.T1088I |
| LUAD | 4 | 177095826 | 177095826 | + | Missense_Mutation | SNP | A | A | G | TCGA-05-5425-01A-02D-1625-08 | TCGA-05-5425-10A-01D-1625-08 | g.chr4:177095826A>G | c.3523A>G | c.(3523-3525)Aga>Gga | p.R1175G |
| LUSC | 4 | 177017731 | 177017731 | + | Missense_Mutation | SNP | C | C | A | TCGA-34-5239-01A-21D-1817-08 | TCGA-34-5239-10A-01D-1817-08 | g.chr4:177017731C>A | c.61C>A | c.(61-63)Caa>Aaa | p.Q21K |
| LUSC | 4 | 177032734 | 177032734 | + | Missense_Mutation | SNP | G | G | A | TCGA-56-6546-01A-11D-1817-08 | TCGA-56-6546-10A-01D-1817-08 | g.chr4:177032734G>A | c.75G>A | c.(73-75)atG>atA | p.M25I |
| LUSC | 4 | 177032751 | 177032751 | + | Missense_Mutation | SNP | T | T | A | TCGA-51-4081-01A-01D-1458-08 | TCGA-51-4081-11A-01D-1458-08 | g.chr4:177032751T>A | c.92T>A | c.(91-93)gTg>gAg | p.V31E |
| LUSC | 4 | 177032792 | 177032792 | + | Missense_Mutation | SNP | G | G | A | TCGA-66-2758-01A-02D-1522-08 | TCGA-66-2758-11A-01D-1522-08 | g.chr4:177032792G>A | c.133G>A | c.(133-135)Gta>Ata | p.V45I |
| LUSC | 4 | 177032832 | 177032833 | + | Missense_Mutation | DNP | CC | CC | AA | TCGA-60-2724-01A-01D-1522-08 | TCGA-60-2724-11A-01D-1522-08 | g.chr4:177032832_177032833CC>AA | c.173_174CC>AA | c.(172-174)aCC>aAA | p.T58K |
| LUSC | 4 | 177052713 | 177052713 | + | Missense_Mutation | SNP | C | C | A | TCGA-34-2600-01A-01D-1522-08 | TCGA-34-2600-11A-01D-1522-08 | g.chr4:177052713C>A | c.994C>A | c.(994-996)Caa>Aaa | p.Q332K |
| LUSC | 4 | 177052851 | 177052851 | + | Missense_Mutation | SNP | G | G | T | TCGA-18-3406-01A-01D-0983-08 | TCGA-18-3406-11A-01D-0983-08 | g.chr4:177052851G>T | c.1132G>T | c.(1132-1134)Gat>Tat | p.D378Y |
| LUSC | 4 | 177056260 | 177056260 | + | Splice_Site | SNP | G | G | A | TCGA-34-5929-01A-11D-1817-08 | TCGA-34-5929-11A-01D-1817-08 | g.chr4:177056260G>A | c.1172G>A | c.(1171-1173)gGa>gAa | p.G391E |
| LUSC | 4 | 177061074 | 177061074 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr4:177061074G>A | c.1463G>A | c.(1462-1464)tGg>tAg | p.W488* |
| LUSC | 4 | 177070988 | 177070988 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr4:177070988C>G | c.2000C>G | c.(1999-2001)aCt>aGt | p.T667S |
| LUSC | 4 | 177070997 | 177070997 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr4:177070997C>G | c.2009C>G | c.(2008-2010)tCt>tGt | p.S670C |
| LUSC | 4 | 177071097 | 177071097 | + | Silent | SNP | T | T | A | TCGA-22-5471-01A-01D-1632-08 | TCGA-22-5471-11A-01D-1632-08 | g.chr4:177071097T>A | c.2109T>A | c.(2107-2109)atT>atA | p.I703I |
| LUSC | 4 | 177072999 | 177072999 | + | Missense_Mutation | SNP | A | A | G | TCGA-85-6560-01A-11D-1817-08 | TCGA-85-6560-10A-01D-1817-08 | g.chr4:177072999A>G | c.2413A>G | c.(2413-2415)Aaa>Gaa | p.K805E |
| LUSC | 4 | 177073061 | 177073061 | + | Silent | SNP | C | C | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr4:177073061C>T | c.2475C>T | c.(2473-2475)atC>atT | p.I825I |
| LUSC | 4 | 177081166 | 177081166 | + | Missense_Mutation | SNP | G | G | T | TCGA-39-5039-01A-01D-1441-08 | TCGA-39-5039-11A-01D-1441-08 | g.chr4:177081166G>T | c.2619G>T | c.(2617-2619)caG>caT | p.Q873H |
| LUSC | 4 | 177081224 | 177081224 | + | Missense_Mutation | SNP | G | G | T | TCGA-21-1076-01A-02D-1521-08 | TCGA-21-1076-11A-01D-1521-08 | g.chr4:177081224G>T | c.2677G>T | c.(2677-2679)Gtc>Ttc | p.V893F |
| LUSC | 4 | 177084335 | 177084335 | + | Missense_Mutation | SNP | G | G | A | TCGA-18-3417-01A-01D-1441-08 | TCGA-18-3417-11A-01D-1441-08 | g.chr4:177084335G>A | c.2953G>A | c.(2953-2955)Gaa>Aaa | p.E985K |
| LUSC | 4 | 177089850 | 177089850 | + | Missense_Mutation | SNP | G | G | T | TCGA-21-5782-01A-01D-1632-08 | TCGA-21-5782-10A-01D-1632-08 | g.chr4:177089850G>T | c.3135G>T | c.(3133-3135)atG>atT | p.M1045I |
| LUSC | 4 | 177094441 | 177094441 | + | Missense_Mutation | SNP | A | A | T | TCGA-46-3767-01A-01D-0983-08 | TCGA-46-3767-10A-01D-0983-08 | g.chr4:177094441A>T | c.3385A>T | c.(3385-3387)Act>Tct | p.T1129S |
| LUSC | 4 | 177098242 | 177098242 | + | Silent | SNP | T | T | A | TCGA-66-2755-01A-01D-1522-08 | TCGA-66-2755-11A-01D-1522-08 | g.chr4:177098242T>A | c.3600T>A | c.(3598-3600)ccT>ccA | p.P1200P |
| LUSC | 4 | 177098633 | 177098633 | + | Missense_Mutation | SNP | A | A | T | TCGA-51-4081-01A-01D-1458-08 | TCGA-51-4081-11A-01D-1458-08 | g.chr4:177098633A>T | c.3677A>T | c.(3676-3678)gAc>gTc | p.D1226V |
| LUSC | 4 | 177098642 | 177098642 | + | Missense_Mutation | SNP | A | A | C | TCGA-22-5471-01A-01D-1632-08 | TCGA-22-5471-11A-01D-1632-08 | g.chr4:177098642A>C | c.3686A>C | c.(3685-3687)tAt>tCt | p.Y1229S |
| LUSC | 4 | 177100702 | 177100702 | + | Missense_Mutation | SNP | G | G | T | TCGA-34-5231-01A-21D-1817-08 | TCGA-34-5231-10A-01D-1817-08 | g.chr4:177100702G>T | c.3941G>T | c.(3940-3942)gGg>gTg | p.G1314V |
| OV | 4 | 177046420 | 177046420 | + | Missense_Mutation | SNP | T | T | C | TCGA-23-1032-01A-02W-0486-08 | TCGA-23-1032-10A-01W-0486-08 | g.chr4:177046420T>C | c.776T>C | c.(775-777)aTa>aCa | p.I259T |
| OV | 4 | 177089798 | 177089798 | + | Splice_Site | SNP | G | G | T | TCGA-61-2012-01A-01W-0722-08 | TCGA-61-2012-11A-01W-0722-08 | g.chr4:177089798G>T | | c.e25-1 | |
| PAAD | 4 | 177052725 | 177052725 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-IB-A7LX-01A-12D-A36O-08 | TCGA-IB-A7LX-10A-01D-A367-08 | g.chr4:177052725delA | c.1006delA | c.(1006-1008)aaafs | p.K336fs |
| PAAD | 4 | 177069319 | 177069319 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr4:177069319G>A | c.1802G>A | c.(1801-1803)tGc>tAc | p.C601Y |
| PAAD | 4 | 177069371 | 177069371 | + | Missense_Mutation | SNP | T | T | A | TCGA-HZ-A8P1-01A-11D-A377-08 | TCGA-HZ-A8P1-10A-01D-A37A-08 | g.chr4:177069371T>A | c.1854T>A | c.(1852-1854)aaT>aaA | p.N618K |
| PAAD | 4 | 177073091 | 177073091 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr4:177073091C>A | c.2505C>A | c.(2503-2505)taC>taA | p.Y835* |
| PAAD | 4 | 177073110 | 177073110 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr4:177073110C>A | c.2524C>A | c.(2524-2526)Ctt>Att | p.L842I |
| PAAD | 4 | 177100634 | 177100634 | + | Silent | SNP | C | C | T | TCGA-FZ-5923-01A-12D-1609-08 | TCGA-FZ-5923-11A-01D-1609-08 | g.chr4:177100634C>T | c.3873C>T | c.(3871-3873)gaC>gaT | p.D1291D |
| PRAD | 4 | 177032828 | 177032828 | + | Missense_Mutation | SNP | G | G | A | TCGA-KC-A7FD-01A-11D-A33T-08 | TCGA-KC-A7FD-10A-01D-A33W-08 | g.chr4:177032828G>A | c.169G>A | c.(169-171)Gcg>Acg | p.A57T |
| PRAD | 4 | 177058695 | 177058695 | + | Missense_Mutation | SNP | G | G | A | TCGA-HI-7170-01A-11D-2114-08 | TCGA-HI-7170-10A-01D-2115-08 | g.chr4:177058695G>A | c.1364G>A | c.(1363-1365)gGa>gAa | p.G455E |
| PRAD | 4 | 177058761 | 177058761 | + | Splice_Site | SNP | A | A | G | TCGA-G9-6329-01A-13D-1961-08 | TCGA-G9-6329-10A-01D-1961-08 | g.chr4:177058761A>G | c.1430A>G | c.(1429-1431)gAg>gGg | p.E477G |
| PRAD | 4 | 177069450 | 177069450 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr4:177069450G>A | c.1933G>A | c.(1933-1935)Gtg>Atg | p.V645M |
| PRAD | 4 | 177071069 | 177071069 | + | Missense_Mutation | SNP | T | T | C | TCGA-J4-A67L-01A-11D-A30E-08 | TCGA-J4-A67L-10A-01D-A30H-08 | g.chr4:177071069T>C | c.2081T>C | c.(2080-2082)cTg>cCg | p.L694P |
| PRAD | 4 | 177083293 | 177083293 | + | Missense_Mutation | SNP | G | G | A | TCGA-EJ-5521-01A-01D-1576-08 | TCGA-EJ-5521-10A-01D-1577-08 | g.chr4:177083293G>A | c.2890G>A | c.(2890-2892)Gca>Aca | p.A964T |
| READ | 4 | 177049909 | 177049909 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:177049909C>T | c.883C>T | c.(883-885)Cgc>Tgc | p.R295C |
| READ | 4 | 177049909 | 177049909 | + | Missense_Mutation | SNP | C | C | T | TCGA-DY-A0XA-01A-11D-A152-10 | TCGA-DY-A0XA-10A-01D-A152-10 | g.chr4:177049909C>T | c.883C>T | c.(883-885)Cgc>Tgc | p.R295C |
| READ | 4 | 177069341 | 177069341 | + | Silent | SNP | C | C | T | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr4:177069341C>T | c.1824C>T | c.(1822-1824)caC>caT | p.H608H |
| READ | 4 | 177093609 | 177093609 | + | Nonsense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:177093609T>G | c.3303T>G | c.(3301-3303)taT>taG | p.Y1101* |
| READ | 4 | 177098225 | 177098225 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:177098225C>T | c.3583C>T | c.(3583-3585)Cgg>Tgg | p.R1195W |
| READ | 4 | 177098286 | 177098286 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:177098286C>T | c.3644C>T | c.(3643-3645)gCt>gTt | p.A1215V |
| READ | 4 | 177100635 | 177100635 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-4007-01A-01W-1073-09 | TCGA-AG-4007-10A-01W-1073-09 | g.chr4:177100635G>A | c.3874G>A | c.(3874-3876)Ggg>Agg | p.G1292R |
| SARC | 4 | 177094499 | 177094499 | + | Nonsense_Mutation | SNP | T | T | G | TCGA-DX-A8BJ-01A-11D-A417-09 | TCGA-DX-A8BJ-10B-01D-A41A-09 | g.chr4:177094499T>G | c.3443T>G | c.(3442-3444)tTa>tGa | p.L1148* |
| SKCM | 4 | 177041199 | 177041199 | + | Silent | SNP | G | G | A | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr4:177041199G>A | c.561G>A | c.(559-561)ggG>ggA | p.G187G |
| SKCM | 4 | 177041212 | 177041212 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr4:177041212G>A | c.574G>A | c.(574-576)Ggt>Agt | p.G192S |
| SKCM | 4 | 177041242 | 177041242 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr4:177041242C>T | c.604C>T | c.(604-606)Cat>Tat | p.H202Y |
| SKCM | 4 | 177041242 | 177041242 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr4:177041242C>T | c.604C>T | c.(604-606)Cat>Tat | p.H202Y |
| SKCM | 4 | 177052741 | 177052741 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr4:177052741C>T | c.1022C>T | c.(1021-1023)tCc>tTc | p.S341F |
| SKCM | 4 | 177052800 | 177052800 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A3F8-06A-11D-A20D-08 | TCGA-DA-A3F8-10A-01D-A20D-08 | g.chr4:177052800C>T | c.1081C>T | c.(1081-1083)Cct>Tct | p.P361S |
| SKCM | 4 | 177056375 | 177056375 | + | Silent | SNP | G | G | A | TCGA-EE-A3JB-06A-11D-A21A-08 | TCGA-EE-A3JB-10A-01D-A21A-08 | g.chr4:177056375G>A | c.1287G>A | c.(1285-1287)gtG>gtA | p.V429V |
| SKCM | 4 | 177056383 | 177056383 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A267-06A-21D-A196-08 | TCGA-GN-A267-10A-01D-A198-08 | g.chr4:177056383C>T | c.1295C>T | c.(1294-1296)tCc>tTc | p.S432F |
| SKCM | 4 | 177056427 | 177056427 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A2A1-06A-11D-A197-08 | TCGA-EE-A2A1-10A-01D-A199-08 | g.chr4:177056427G>A | c.1339G>A | c.(1339-1341)Ggt>Agt | p.G447S |
| SKCM | 4 | 177063141 | 177063141 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr4:177063141C>T | c.1522C>T | c.(1522-1524)Cga>Tga | p.R508* |
| SKCM | 4 | 177067188 | 177067188 | + | Silent | SNP | T | T | A | TCGA-DA-A1I8-06A-11D-A197-08 | TCGA-DA-A1I8-10A-01D-A199-08 | g.chr4:177067188T>A | c.1644T>A | c.(1642-1644)gtT>gtA | p.V548V |
| SKCM | 4 | 177067288 | 177067288 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr4:177067288C>T | c.1744C>T | c.(1744-1746)Ctt>Ttt | p.L582F |
| SKCM | 4 | 177069353 | 177069353 | + | Silent | SNP | G | G | A | TCGA-EE-A29G-06A-12D-A196-08 | TCGA-EE-A29G-10A-01D-A198-08 | g.chr4:177069353G>A | c.1836G>A | c.(1834-1836)gtG>gtA | p.V612V |
| SKCM | 4 | 177069382 | 177069382 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr4:177069382C>T | c.1865C>T | c.(1864-1866)cCa>cTa | p.P622L |
| SKCM | 4 | 177071078 | 177071078 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr4:177071078G>A | c.2090G>A | c.(2089-2091)aGa>aAa | p.R697K |
| SKCM | 4 | 177093643 | 177093643 | + | Missense_Mutation | SNP | C | C | T | TCGA-RP-A695-06A-11D-A30X-08 | TCGA-RP-A695-10A-01D-A30X-08 | g.chr4:177093643C>T | c.3337C>T | c.(3337-3339)Cct>Tct | p.P1113S |
| SKCM | 4 | 177094490 | 177094490 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr4:177094490C>T | c.3434C>T | c.(3433-3435)aCt>aTt | p.T1145I |
| SKCM | 4 | 177098301 | 177098301 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr4:177098301C>T | c.3659C>T | c.(3658-3660)aCc>aTc | p.T1220I |
| SKCM | 4 | 177098682 | 177098682 | + | Silent | SNP | T | T | G | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr4:177098682T>G | c.3726T>G | c.(3724-3726)acT>acG | p.T1242T |
| SKCM | 4 | 177098790 | 177098790 | + | Silent | SNP | G | G | A | TCGA-D3-A51F-06A-11D-A25O-08 | TCGA-D3-A51F-10A-01D-A25O-08 | g.chr4:177098790G>A | c.3834G>A | c.(3832-3834)acG>acA | p.T1278T |
| SKCM | 4 | 177100651 | 177100651 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GN-06A-11D-A27K-08 | TCGA-D3-A5GN-10A-01D-A27N-08 | g.chr4:177100651C>T | c.3890C>T | c.(3889-3891)tCc>tTc | p.S1297F |
| SKCM | 4 | 177100682 | 177100682 | + | Silent | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr4:177100682G>A | c.3921G>A | c.(3919-3921)gtG>gtA | p.V1307V |
| SKCM | 4 | 177100687 | 177100687 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr4:177100687C>T | c.3926C>T | c.(3925-3927)cCa>cTa | p.P1309L |