| Mutation - TCGA |
| Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
|---|
| BLCA | 3 | 120871362 | 120871362 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A6TB-01A-12D-A339-08 | TCGA-FD-A6TB-10A-21D-A339-08 | g.chr3:120871362G>C | c.708G>C | c.(706-708)tgG>tgC | p.W236C |
| BLCA | 3 | 120871392 | 120871392 | + | Missense_Mutation | SNP | A | A | C | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr3:120871392A>C | c.738A>C | c.(736-738)agA>agC | p.R246S |
| BLCA | 3 | 120941851 | 120941851 | + | Splice_Site | SNP | G | G | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr3:120941851G>A | c.958G>A | c.(958-960)Gaa>Aaa | p.E320K |
| BLCA | 3 | 120973778 | 120973778 | + | Missense_Mutation | SNP | A | A | T | TCGA-C4-A0F0-01A-12D-A10S-08 | TCGA-C4-A0F0-10A-01D-A10S-08 | g.chr3:120973778A>T | c.1478A>T | c.(1477-1479)aAa>aTa | p.K493I |
| BLCA | 3 | 120976135 | 120976135 | + | Missense_Mutation | SNP | C | C | G | TCGA-4Z-AA84-01A-11D-A391-08 | TCGA-4Z-AA84-10A-01D-A394-08 | g.chr3:120976135C>G | c.1787C>G | c.(1786-1788)aCt>aGt | p.T596S |
| BLCA | 3 | 120976150 | 120976150 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A5BZ-01A-11D-A289-08 | TCGA-FD-A5BZ-10A-01D-A289-08 | g.chr3:120976150G>C | c.1802G>C | c.(1801-1803)gGa>gCa | p.G601A |
| BLCA | 3 | 121001120 | 121001120 | + | Missense_Mutation | SNP | T | T | G | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr3:121001120T>G | c.2118T>G | c.(2116-2118)ttT>ttG | p.F706L |
| BLCA | 3 | 121037357 | 121037362 | + | In_Frame_Del | DEL | GAACTT | GAACTT | - | TCGA-GU-AATP-01A-11D-A391-08 | TCGA-GU-AATP-10A-01D-A394-08 | g.chr3:121037357_121037362delGAACTT | c.2218_2223delGAACTT | c.(2218-2223)gaacttdel | p.EL740del |
| BLCA | 3 | 121100143 | 121100143 | + | Missense_Mutation | SNP | A | A | C | TCGA-4Z-AA87-01A-11D-A391-08 | TCGA-4Z-AA87-10A-01D-A394-08 | g.chr3:121100143A>C | c.2423A>C | c.(2422-2424)aAc>aCc | p.N808T |
| BLCA | 3 | 121100203 | 121100203 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr3:121100203C>G | c.2483C>G | c.(2482-2484)tCt>tGt | p.S828C |
| BLCA | 3 | 121126442 | 121126442 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SN-01A-12D-A22Z-08 | TCGA-FD-A3SN-10A-01D-A22Z-08 | g.chr3:121126442G>A | c.3012G>A | c.(3010-3012)atG>atA | p.M1004I |
| BLCA | 3 | 121132110 | 121132110 | + | Silent | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr3:121132110C>T | c.3126C>T | c.(3124-3126)ctC>ctT | p.L1042L |
| BLCA | 3 | 121132123 | 121132123 | + | Missense_Mutation | SNP | G | G | C | TCGA-G2-AA3D-01A-11D-A391-08 | TCGA-G2-AA3D-10A-01D-A394-08 | g.chr3:121132123G>C | c.3139G>C | c.(3139-3141)Gaa>Caa | p.E1047Q |
| BLCA | 3 | 121134743 | 121134743 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A6B2-01A-11D-A30E-08 | TCGA-DK-A6B2-10A-01D-A30H-08 | g.chr3:121134743G>C | c.3226G>C | c.(3226-3228)Gaa>Caa | p.E1076Q |
| BLCA | 3 | 121137298 | 121137298 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A2LD-01A-12D-A20D-08 | TCGA-BT-A2LD-10A-01D-A20D-08 | g.chr3:121137298G>A | c.3413G>A | c.(3412-3414)cGt>cAt | p.R1138H |
| BLCA | 3 | 121137304 | 121137304 | + | Missense_Mutation | SNP | G | G | T | TCGA-FD-A3B3-01A-12D-A202-08 | TCGA-FD-A3B3-10A-01D-A202-08 | g.chr3:121137304G>T | c.3419G>T | c.(3418-3420)cGg>cTg | p.R1140L |
| BRCA | 3 | 120952485 | 120952485 | + | Silent | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr3:120952485C>T | c.1134C>T | c.(1132-1134)gtC>gtT | p.V378V |
| BRCA | 3 | 120957891 | 120957891 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr3:120957891G>C | c.1258G>C | c.(1258-1260)Gat>Cat | p.D420H |
| BRCA | 3 | 120973931 | 120973931 | + | Missense_Mutation | SNP | G | G | A | TCGA-A2-A0CX-01A-21W-A019-09 | TCGA-A2-A0CX-10A-01W-A021-09 | g.chr3:120973931G>A | c.1631G>A | c.(1630-1632)aGc>aAc | p.S544N |
| BRCA | 3 | 120977986 | 120977986 | + | Silent | SNP | T | T | C | TCGA-A7-A5ZV-01A-11D-A28B-09 | TCGA-A7-A5ZV-10A-01D-A28E-09 | g.chr3:120977986T>C | c.1929T>C | c.(1927-1929)acT>acC | p.T643T |
| BRCA | 3 | 121097679 | 121097679 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr3:121097679C>T | c.2365C>T | c.(2365-2367)Cga>Tga | p.R789* |
| BRCA | 3 | 121137241 | 121137241 | + | Missense_Mutation | SNP | C | C | T | TCGA-E9-A1R7-01A-11D-A14K-09 | TCGA-E9-A1R7-10A-01D-A14K-09 | g.chr3:121137241C>T | c.3356C>T | c.(3355-3357)cCa>cTa | p.P1119L |
| CESC | 3 | 120957831 | 120957831 | + | Missense_Mutation | SNP | G | G | C | TCGA-C5-A7CO-01A-11D-A351-09 | TCGA-C5-A7CO-10A-01D-A351-09 | g.chr3:120957831G>C | c.1198G>C | c.(1198-1200)Gaa>Caa | p.E400Q |
| CESC | 3 | 120998662 | 120998662 | + | Missense_Mutation | SNP | G | G | C | TCGA-C5-A2LX-01A-11D-A18J-09 | TCGA-C5-A2LX-10A-01D-A18J-09 | g.chr3:120998662G>C | c.1969G>C | c.(1969-1971)Ggg>Cgg | p.G657R |
| CESC | 3 | 121132054 | 121132054 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A2LX-01A-11D-A18J-09 | TCGA-C5-A2LX-10A-01D-A18J-09 | g.chr3:121132054G>A | c.3070G>A | c.(3070-3072)Gac>Aac | p.D1024N |
| COAD | 3 | 120628498 | 120628498 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr3:120628498G>T | c.73G>T | c.(73-75)Ggc>Tgc | p.G25C |
| COAD | 3 | 120673816 | 120673816 | + | Silent | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr3:120673816C>T | c.219C>T | c.(217-219)ccC>ccT | p.P73P |
| COAD | 3 | 120760617 | 120760617 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr3:120760617T>G | c.358T>G | c.(358-360)Ttg>Gtg | p.L120V |
| COAD | 3 | 120764286 | 120764286 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-5539-01A-01D-1650-10 | TCGA-D5-5539-10A-01D-1650-10 | g.chr3:120764286C>T | c.374C>T | c.(373-375)gCc>gTc | p.A125V |
| COAD | 3 | 120876375 | 120876375 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr3:120876375C>A | c.778C>A | c.(778-780)Cat>Aat | p.H260N |
| COAD | 3 | 120941991 | 120941991 | + | Silent | SNP | G | G | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr3:120941991G>A | c.1098G>A | c.(1096-1098)acG>acA | p.T366T |
| COAD | 3 | 120952519 | 120952519 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3982-01A-02W-0995-10 | TCGA-AA-3982-10A-01W-0999-10 | g.chr3:120952519G>T | c.1168G>T | c.(1168-1170)Gat>Tat | p.D390Y |
| COAD | 3 | 120957909 | 120957909 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr3:120957909A>G | c.1276A>G | c.(1276-1278)Att>Gtt | p.I426V |
| COAD | 3 | 120957910 | 120957910 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr3:120957910T>C | c.1277T>C | c.(1276-1278)aTt>aCt | p.I426T |
| COAD | 3 | 120957933 | 120957933 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr3:120957933G>A | c.1300G>A | c.(1300-1302)Gtc>Atc | p.V434I |
| COAD | 3 | 120973862 | 120973862 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5860-01A-01D-1650-10 | TCGA-CM-5860-10A-01D-1650-10 | g.chr3:120973862A>G | c.1562A>G | c.(1561-1563)tAc>tGc | p.Y521C |
| COAD | 3 | 121001127 | 121001127 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr3:121001127C>T | c.2125C>T | c.(2125-2127)Cgt>Tgt | p.R709C |
| COAD | 3 | 121097679 | 121097679 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr3:121097679C>T | c.2365C>T | c.(2365-2367)Cga>Tga | p.R789* |
| COAD | 3 | 121126141 | 121126141 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr3:121126141G>A | c.2711G>A | c.(2710-2712)cGa>cAa | p.R904Q |
| COAD | 3 | 121126405 | 121126405 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr3:121126405C>T | c.2975C>T | c.(2974-2976)gCc>gTc | p.A992V |
| COAD | 3 | 121132024 | 121132024 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3697-01A-01D-1719-10 | TCGA-AA-3697-11A-01D-1719-10 | g.chr3:121132024A>C | c.3040A>C | c.(3040-3042)Atg>Ctg | p.M1014L |
| COAD | 3 | 121134716 | 121134716 | + | Missense_Mutation | SNP | G | G | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr3:121134716G>T | c.3199G>T | c.(3199-3201)Gat>Tat | p.D1067Y |
| COAD | 3 | 121134764 | 121134764 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr3:121134764C>T | c.3247C>T | c.(3247-3249)Ctc>Ttc | p.L1083F |
| COAD | 3 | 121137247 | 121137247 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-6600-01A-11D-1771-10 | TCGA-AZ-6600-11A-01D-1771-10 | g.chr3:121137247G>T | c.3362G>T | c.(3361-3363)aGt>aTt | p.S1121I |
| COADREAD | 3 | 120628436 | 120628436 | + | Missense_Mutation | SNP | T | T | C | TCGA-F5-6702-01A-11D-1826-10 | TCGA-F5-6702-10A-01D-1826-10 | g.chr3:120628436T>C | c.11T>C | c.(10-12)tTt>tCt | p.F4S |
| COADREAD | 3 | 120628498 | 120628498 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr3:120628498G>T | c.73G>T | c.(73-75)Ggc>Tgc | p.G25C |
| COADREAD | 3 | 120673816 | 120673816 | + | Silent | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr3:120673816C>T | c.219C>T | c.(217-219)ccC>ccT | p.P73P |
| COADREAD | 3 | 120760617 | 120760617 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr3:120760617T>G | c.358T>G | c.(358-360)Ttg>Gtg | p.L120V |
| COADREAD | 3 | 120764286 | 120764286 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-5539-01A-01D-1650-10 | TCGA-D5-5539-10A-01D-1650-10 | g.chr3:120764286C>T | c.374C>T | c.(373-375)gCc>gTc | p.A125V |
| COADREAD | 3 | 120876375 | 120876375 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr3:120876375C>A | c.778C>A | c.(778-780)Cat>Aat | p.H260N |
| COADREAD | 3 | 120924773 | 120924773 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:120924773A>C | c.881A>C | c.(880-882)aAa>aCa | p.K294T |
| COADREAD | 3 | 120941991 | 120941991 | + | Silent | SNP | G | G | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr3:120941991G>A | c.1098G>A | c.(1096-1098)acG>acA | p.T366T |
| COADREAD | 3 | 120952519 | 120952519 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3982-01A-02W-0995-10 | TCGA-AA-3982-10A-01W-0999-10 | g.chr3:120952519G>T | c.1168G>T | c.(1168-1170)Gat>Tat | p.D390Y |
| COADREAD | 3 | 120957909 | 120957909 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr3:120957909A>G | c.1276A>G | c.(1276-1278)Att>Gtt | p.I426V |
| COADREAD | 3 | 120957910 | 120957910 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr3:120957910T>C | c.1277T>C | c.(1276-1278)aTt>aCt | p.I426T |
| COADREAD | 3 | 120957933 | 120957933 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr3:120957933G>A | c.1300G>A | c.(1300-1302)Gtc>Atc | p.V434I |
| COADREAD | 3 | 120973862 | 120973862 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5860-01A-01D-1650-10 | TCGA-CM-5860-10A-01D-1650-10 | g.chr3:120973862A>G | c.1562A>G | c.(1561-1563)tAc>tGc | p.Y521C |
| COADREAD | 3 | 120973920 | 120973920 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:120973920T>G | c.1620T>G | c.(1618-1620)atT>atG | p.I540M |
| COADREAD | 3 | 121001127 | 121001127 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr3:121001127C>T | c.2125C>T | c.(2125-2127)Cgt>Tgt | p.R709C |
| COADREAD | 3 | 121097652 | 121097652 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:121097652C>T | c.2338C>T | c.(2338-2340)Cgc>Tgc | p.R780C |
| COADREAD | 3 | 121097679 | 121097679 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr3:121097679C>T | c.2365C>T | c.(2365-2367)Cga>Tga | p.R789* |
| COADREAD | 3 | 121126141 | 121126141 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr3:121126141G>A | c.2711G>A | c.(2710-2712)cGa>cAa | p.R904Q |
| COADREAD | 3 | 121126405 | 121126405 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr3:121126405C>T | c.2975C>T | c.(2974-2976)gCc>gTc | p.A992V |
| COADREAD | 3 | 121132024 | 121132024 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3697-01A-01D-1719-10 | TCGA-AA-3697-11A-01D-1719-10 | g.chr3:121132024A>C | c.3040A>C | c.(3040-3042)Atg>Ctg | p.M1014L |
| COADREAD | 3 | 121134716 | 121134716 | + | Missense_Mutation | SNP | G | G | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr3:121134716G>T | c.3199G>T | c.(3199-3201)Gat>Tat | p.D1067Y |
| COADREAD | 3 | 121134764 | 121134764 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr3:121134764C>T | c.3247C>T | c.(3247-3249)Ctc>Ttc | p.L1083F |
| COADREAD | 3 | 121137247 | 121137247 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-6600-01A-11D-1771-10 | TCGA-AZ-6600-11A-01D-1771-10 | g.chr3:121137247G>T | c.3362G>T | c.(3361-3363)aGt>aTt | p.S1121I |
| ESCA | 3 | 120760584 | 120760584 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-VR-A8EX-01A-11D-A36J-09 | TCGA-VR-A8EX-10A-01D-A36M-09 | g.chr3:120760584G>T | c.325G>T | c.(325-327)Gaa>Taa | p.E109* |
| ESCA | 3 | 120840538 | 120840538 | + | Missense_Mutation | SNP | G | G | C | TCGA-LN-A4A9-01A-11D-A28B-09 | TCGA-LN-A4A9-10A-01D-A28E-09 | g.chr3:120840538G>C | c.656G>C | c.(655-657)aGa>aCa | p.R219T |
| ESCA | 3 | 120957831 | 120957831 | + | Missense_Mutation | SNP | G | G | A | TCGA-Z6-AAPN-01A-11D-A403-09 | TCGA-Z6-AAPN-10A-01D-A403-09 | g.chr3:120957831G>A | c.1198G>A | c.(1198-1200)Gaa>Aaa | p.E400K |
| ESCA | 3 | 121100248 | 121100248 | + | Missense_Mutation | SNP | G | G | A | TCGA-VR-A8EW-01A-11D-A36J-09 | TCGA-VR-A8EW-10A-01D-A36M-09 | g.chr3:121100248G>A | c.2528G>A | c.(2527-2529)cGg>cAg | p.R843Q |
| ESCA | 3 | 121100286 | 121100286 | + | Missense_Mutation | SNP | G | G | C | TCGA-XP-A8T8-01A-11D-A36J-09 | TCGA-XP-A8T8-10A-01D-A36M-09 | g.chr3:121100286G>C | c.2566G>C | c.(2566-2568)Gga>Cga | p.G856R |
| ESCA | 3 | 121126164 | 121126164 | + | Missense_Mutation | SNP | C | C | T | TCGA-JY-A93F-01A-21D-A37C-09 | TCGA-JY-A93F-10A-01D-A37F-09 | g.chr3:121126164C>T | c.2734C>T | c.(2734-2736)Cca>Tca | p.P912S |
| ESCA | 3 | 121137298 | 121137298 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A43E-01A-11D-A247-09 | TCGA-L5-A43E-10A-01D-A247-09 | g.chr3:121137298G>A | c.3413G>A | c.(3412-3414)cGt>cAt | p.R1138H |
| GBM | 3 | 120764376 | 120764376 | + | Missense_Mutation | SNP | G | G | A | TCGA-32-1970-01A-01D-1494-08 | TCGA-32-1970-10A-01D-1494-08 | g.chr3:120764376G>A | c.464G>A | c.(463-465)cGg>cAg | p.R155Q |
| GBM | 3 | 120833881 | 120833881 | + | Missense_Mutation | SNP | A | A | G | TCGA-26-5139-01A-01D-1486-08 | TCGA-26-5139-10A-01D-1486-08 | g.chr3:120833881A>G | c.580A>G | c.(580-582)Atc>Gtc | p.I194V |
| GBM | 3 | 120871386 | 120871386 | + | Silent | SNP | A | A | G | TCGA-32-4209-01A-01D-1353-08 | TCGA-32-4209-10A-01D-1353-08 | g.chr3:120871386A>G | c.732A>G | c.(730-732)gaA>gaG | p.E244E |
| GBM | 3 | 120957900 | 120957900 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-5207-01A-01D-1486-08 | TCGA-28-5207-10A-01D-1486-08 | g.chr3:120957900C>T | c.1267C>T | c.(1267-1269)Ccg>Tcg | p.P423S |
| GBM | 3 | 120976169 | 120976169 | + | Missense_Mutation | SNP | T | T | G | TCGA-81-5910-01A-11D-1696-08 | TCGA-81-5910-10A-01D-1696-08 | g.chr3:120976169T>G | c.1821T>G | c.(1819-1821)atT>atG | p.I607M |
| GBM | 3 | 121126274 | 121126274 | + | Missense_Mutation | SNP | G | G | C | TCGA-06-0157-01A-01D-1491-08 | TCGA-06-0157-10A-01D-1491-08 | g.chr3:121126274G>C | c.2844G>C | c.(2842-2844)caG>caC | p.Q948H |
| GBMLGG | 3 | 120628568 | 120628569 | + | In_Frame_Ins | INS | - | - | CGC | TCGA-HT-7884-01B-11D-2395-08 | TCGA-HT-7884-10A-01D-2396-08 | g.chr3:120628568_120628569insCGC | c.143_144insCGC | c.(142-147)gaggaa>gaCGCggaa | p.48_48E>DA |
| GBMLGG | 3 | 120764376 | 120764376 | + | Missense_Mutation | SNP | G | G | A | TCGA-32-1970-01A-01D-1494-08 | TCGA-32-1970-10A-01D-1494-08 | g.chr3:120764376G>A | c.464G>A | c.(463-465)cGg>cAg | p.R155Q |
| GBMLGG | 3 | 120833881 | 120833881 | + | Missense_Mutation | SNP | A | A | G | TCGA-26-5139-01A-01D-1486-08 | TCGA-26-5139-10A-01D-1486-08 | g.chr3:120833881A>G | c.580A>G | c.(580-582)Atc>Gtc | p.I194V |
| GBMLGG | 3 | 120871386 | 120871386 | + | Silent | SNP | A | A | G | TCGA-32-4209-01A-01D-1353-08 | TCGA-32-4209-10A-01D-1353-08 | g.chr3:120871386A>G | c.732A>G | c.(730-732)gaA>gaG | p.E244E |
| GBMLGG | 3 | 120957900 | 120957900 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-5207-01A-01D-1486-08 | TCGA-28-5207-10A-01D-1486-08 | g.chr3:120957900C>T | c.1267C>T | c.(1267-1269)Ccg>Tcg | p.P423S |
| GBMLGG | 3 | 120976169 | 120976169 | + | Missense_Mutation | SNP | T | T | G | TCGA-81-5910-01A-11D-1696-08 | TCGA-81-5910-10A-01D-1696-08 | g.chr3:120976169T>G | c.1821T>G | c.(1819-1821)atT>atG | p.I607M |
| GBMLGG | 3 | 121097685 | 121097685 | + | Missense_Mutation | SNP | G | G | T | TCGA-HT-A5RC-01A-11D-A289-08 | TCGA-HT-A5RC-10A-01D-A289-08 | g.chr3:121097685G>T | c.2371G>T | c.(2371-2373)Gcc>Tcc | p.A791S |
| GBMLGG | 3 | 121126116 | 121126116 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:121126116G>A | c.2686G>A | c.(2686-2688)Gtg>Atg | p.V896M |
| GBMLGG | 3 | 121126125 | 121126125 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:121126125T>C | c.2695T>C | c.(2695-2697)Ttc>Ctc | p.F899L |
| GBMLGG | 3 | 121126274 | 121126274 | + | Missense_Mutation | SNP | G | G | C | TCGA-06-0157-01A-01D-1491-08 | TCGA-06-0157-10A-01D-1491-08 | g.chr3:121126274G>C | c.2844G>C | c.(2842-2844)caG>caC | p.Q948H |
| HNSC | 3 | 120760566 | 120760566 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-A63Y-01A-11D-A30E-08 | TCGA-CN-A63Y-10A-01D-A30H-08 | g.chr3:120760566G>A | c.307G>A | c.(307-309)Gat>Aat | p.D103N |
| HNSC | 3 | 120941894 | 120941894 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-6441-01A-11D-1683-08 | TCGA-CV-6441-11A-01D-1683-08 | g.chr3:120941894C>A | c.1001C>A | c.(1000-1002)gCt>gAt | p.A334D |
| HNSC | 3 | 120941922 | 120941922 | + | Missense_Mutation | SNP | G | G | T | TCGA-BA-A6DA-01A-31D-A31L-08 | TCGA-BA-A6DA-10A-01D-A31J-08 | g.chr3:120941922G>T | c.1029G>T | c.(1027-1029)atG>atT | p.M343I |
| HNSC | 3 | 120976074 | 120976074 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-A6V1-01A-12D-A34J-08 | TCGA-CN-A6V1-10B-01D-A34M-08 | g.chr3:120976074C>T | c.1726C>T | c.(1726-1728)Ccg>Tcg | p.P576S |
| HNSC | 3 | 120976119 | 120976119 | + | Missense_Mutation | SNP | T | T | A | TCGA-P3-A6T7-01A-11D-A34J-08 | TCGA-P3-A6T7-10A-01D-A34M-08 | g.chr3:120976119T>A | c.1771T>A | c.(1771-1773)Tct>Act | p.S591T |
| HNSC | 3 | 120977900 | 120977900 | + | Missense_Mutation | SNP | C | C | T | TCGA-CR-7394-01A-11D-2012-08 | TCGA-CR-7394-10A-01D-2013-08 | g.chr3:120977900C>T | c.1843C>T | c.(1843-1845)Cgg>Tgg | p.R615W |
| HNSC | 3 | 120977960 | 120977960 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-5369-01A-01D-1434-08 | TCGA-CN-5369-10A-01D-1434-08 | g.chr3:120977960G>C | c.1903G>C | c.(1903-1905)Gat>Cat | p.D635H |
| HNSC | 3 | 120998664 | 120998664 | + | Silent | SNP | G | G | T | TCGA-CR-7388-01A-11D-2012-08 | TCGA-CR-7388-10A-01D-2013-08 | g.chr3:120998664G>T | c.1971G>T | c.(1969-1971)ggG>ggT | p.G657G |
| HNSC | 3 | 120998674 | 120998674 | + | Missense_Mutation | SNP | G | G | A | TCGA-BA-A6DI-01A-11D-A30E-08 | TCGA-BA-A6DI-10A-01D-A30H-08 | g.chr3:120998674G>A | c.1981G>A | c.(1981-1983)Ggg>Agg | p.G661R |
| HNSC | 3 | 120998716 | 120998716 | + | Missense_Mutation | SNP | A | A | G | TCGA-CV-7097-01A-11D-2012-08 | TCGA-CV-7097-10A-01D-2013-08 | g.chr3:120998716A>G | c.2023A>G | c.(2023-2025)Agc>Ggc | p.S675G |
| HNSC | 3 | 120998727 | 120998727 | + | Silent | SNP | C | C | T | TCGA-CX-7086-01A-11D-2078-08 | TCGA-CX-7086-10D-01D-2078-08 | g.chr3:120998727C>T | c.2034C>T | c.(2032-2034)acC>acT | p.T678T |
| HNSC | 3 | 121001149 | 121001149 | + | Missense_Mutation | SNP | C | C | A | TCGA-CR-7402-01A-11D-2012-08 | TCGA-CR-7402-10A-01D-2013-08 | g.chr3:121001149C>A | c.2147C>A | c.(2146-2148)cCt>cAt | p.P716H |
| HNSC | 3 | 121097619 | 121097619 | + | Missense_Mutation | SNP | C | C | T | TCGA-QK-A6II-01A-11D-A31L-08 | TCGA-QK-A6II-10A-01D-A31J-08 | g.chr3:121097619C>T | c.2305C>T | c.(2305-2307)Cgt>Tgt | p.R769C |
| HNSC | 3 | 121100262 | 121100262 | + | Missense_Mutation | SNP | A | A | G | TCGA-CN-4735-01A-01D-1434-08 | TCGA-CN-4735-10A-01D-1434-08 | g.chr3:121100262A>G | c.2542A>G | c.(2542-2544)Acc>Gcc | p.T848A |
| HNSC | 3 | 121126200 | 121126200 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-A63Y-01A-11D-A30E-08 | TCGA-CN-A63Y-10A-01D-A30H-08 | g.chr3:121126200G>A | c.2770G>A | c.(2770-2772)Gaa>Aaa | p.E924K |
| HNSC | 3 | 121132062 | 121132062 | + | Silent | SNP | G | G | A | TCGA-CV-A463-01A-11D-A25Y-08 | TCGA-CV-A463-10A-01D-A25Y-08 | g.chr3:121132062G>A | c.3078G>A | c.(3076-3078)agG>agA | p.R1026R |
| KIPAN | 3 | 121097679 | 121097679 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-B0-5115-01A-01D-1421-08 | TCGA-B0-5115-11A-01D-1421-08 | g.chr3:121097679C>T | c.2365C>T | c.(2365-2367)Cga>Tga | p.R789* |
| KIPAN | 3 | 121100364 | 121100367 | + | Frame_Shift_Del | DEL | ATGG | ATGG | - | TCGA-UZ-A9Q0-01A-12D-A42J-10 | TCGA-UZ-A9Q0-10A-01D-A42M-10 | g.chr3:121100364_121100367delATGG | c.2644_2647delATGG | c.(2644-2649)atggtafs | p.MV882fs |
| KIPAN | 3 | 121137382 | 121137382 | + | Missense_Mutation | SNP | C | C | T | TCGA-B0-5705-01A-11D-1534-10 | TCGA-B0-5705-11A-01D-1534-10 | g.chr3:121137382C>T | c.3497C>T | c.(3496-3498)gCa>gTa | p.A1166V |
| KIRC | 3 | 121097679 | 121097679 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-B0-5115-01A-01D-1421-08 | TCGA-B0-5115-11A-01D-1421-08 | g.chr3:121097679C>T | c.2365C>T | c.(2365-2367)Cga>Tga | p.R789* |
| KIRC | 3 | 121137382 | 121137382 | + | Missense_Mutation | SNP | C | C | T | TCGA-B0-5705-01A-11D-1534-10 | TCGA-B0-5705-11A-01D-1534-10 | g.chr3:121137382C>T | c.3497C>T | c.(3496-3498)gCa>gTa | p.A1166V |
| KIRP | 3 | 121100364 | 121100367 | + | Frame_Shift_Del | DEL | ATGG | ATGG | - | TCGA-UZ-A9Q0-01A-12D-A42J-10 | TCGA-UZ-A9Q0-10A-01D-A42M-10 | g.chr3:121100364_121100367delATGG | c.2644_2647delATGG | c.(2644-2649)atggtafs | p.MV882fs |
| LAML | 3 | 121097619 | 121097619 | + | Missense_Mutation | SNP | C | C | T | TCGA-AB-2833-03B-01W-0728-08 | TCGA-AB-2833-11B-01W-0729-08 | g.chr3:121097619C>T | c.2305C>T | c.(2305-2307)Cgt>Tgt | p.R769C |
| LGG | 3 | 120628568 | 120628569 | + | In_Frame_Ins | INS | - | - | CGC | TCGA-HT-7884-01B-11D-2395-08 | TCGA-HT-7884-10A-01D-2396-08 | g.chr3:120628568_120628569insCGC | c.143_144insCGC | c.(142-147)gaggaa>gaCGCggaa | p.48_48E>DA |
| LGG | 3 | 121097685 | 121097685 | + | Missense_Mutation | SNP | G | G | T | TCGA-HT-A5RC-01A-11D-A289-08 | TCGA-HT-A5RC-10A-01D-A289-08 | g.chr3:121097685G>T | c.2371G>T | c.(2371-2373)Gcc>Tcc | p.A791S |
| LGG | 3 | 121126116 | 121126116 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:121126116G>A | c.2686G>A | c.(2686-2688)Gtg>Atg | p.V896M |
| LGG | 3 | 121126125 | 121126125 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:121126125T>C | c.2695T>C | c.(2695-2697)Ttc>Ctc | p.F899L |
| LIHC | 3 | 120871322 | 120871322 | + | Splice_Site | SNP | A | A | G | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr3:120871322A>G | | c.e8-1 | |
| LIHC | 3 | 120876465 | 120876465 | + | Missense_Mutation | SNP | A | A | G | TCGA-FV-A23B-01A-11D-A16V-10 | TCGA-FV-A23B-11A-11D-A16V-10 | g.chr3:120876465A>G | c.868A>G | c.(868-870)Att>Gtt | p.I290V |
| LIHC | 3 | 120941851 | 120941851 | + | Splice_Site | SNP | G | G | A | TCGA-ED-A82E-01A-11D-A34Z-10 | TCGA-ED-A82E-10A-01D-A34Z-10 | g.chr3:120941851G>A | c.958G>A | c.(958-960)Gaa>Aaa | p.E320K |
| LIHC | 3 | 120941904 | 120941904 | + | Silent | SNP | A | A | G | TCGA-DD-A39X-01A-11D-A20W-10 | TCGA-DD-A39X-11A-11D-A20W-10 | g.chr3:120941904A>G | c.1011A>G | c.(1009-1011)agA>agG | p.R337R |
| LIHC | 3 | 120941989 | 120941989 | + | Missense_Mutation | SNP | A | A | G | TCGA-CC-A3MB-01A-11D-A20W-10 | TCGA-CC-A3MB-10A-01D-A20W-10 | g.chr3:120941989A>G | c.1096A>G | c.(1096-1098)Acg>Gcg | p.T366A |
| LIHC | 3 | 120959330 | 120959330 | + | Missense_Mutation | SNP | C | C | G | TCGA-DD-A73G-01A-22D-A32G-10 | TCGA-DD-A73G-10A-01D-A32G-10 | g.chr3:120959330C>G | c.1376C>G | c.(1375-1377)aCa>aGa | p.T459R |
| LIHC | 3 | 120976155 | 120976155 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-A3A1-01A-11D-A20W-10 | TCGA-DD-A3A1-11A-11D-A20W-10 | g.chr3:120976155A>G | c.1807A>G | c.(1807-1809)Aca>Gca | p.T603A |
| LIHC | 3 | 120998775 | 120998775 | + | Silent | SNP | T | T | A | TCGA-DD-AACV-01A-11D-A40R-10 | TCGA-DD-AACV-10A-01D-A40U-10 | g.chr3:120998775T>A | c.2082T>A | c.(2080-2082)tcT>tcA | p.S694S |
| LIHC | 3 | 121001118 | 121001118 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr3:121001118delT | c.2116delT | c.(2116-2118)tttfs | p.F706fs |
| LIHC | 3 | 121126301 | 121126301 | + | Missense_Mutation | SNP | A | A | T | TCGA-XR-A8TF-01A-11D-A35Z-10 | TCGA-XR-A8TF-10A-01D-A35Z-10 | g.chr3:121126301A>T | c.2871A>T | c.(2869-2871)caA>caT | p.Q957H |
| LUAD | 3 | 120628540 | 120628540 | + | Missense_Mutation | SNP | C | C | A | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr3:120628540C>A | c.115C>A | c.(115-117)Ccg>Acg | p.P39T |
| LUAD | 3 | 120673790 | 120673790 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z030-01A-01W-0746-08 | TCGA-17-Z030-11A-01W-0746-08 | g.chr3:120673790G>T | c.193G>T | c.(193-195)Gtt>Ttt | p.V65F |
| LUAD | 3 | 120673850 | 120673850 | + | Missense_Mutation | SNP | T | T | G | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr3:120673850T>G | c.253T>G | c.(253-255)Ttg>Gtg | p.L85V |
| LUAD | 3 | 120764291 | 120764291 | + | Missense_Mutation | SNP | G | G | A | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr3:120764291G>A | c.379G>A | c.(379-381)Gtc>Atc | p.V127I |
| LUAD | 3 | 120764330 | 120764330 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr3:120764330C>A | c.418C>A | c.(418-420)Ctt>Att | p.L140I |
| LUAD | 3 | 120871405 | 120871405 | + | Missense_Mutation | SNP | G | G | A | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr3:120871405G>A | c.751G>A | c.(751-753)Gag>Aag | p.E251K |
| LUAD | 3 | 120871407 | 120871407 | + | Splice_Site | SNP | G | G | T | TCGA-78-7536-01A-11D-2063-08 | TCGA-78-7536-10A-01D-2063-08 | g.chr3:120871407G>T | c.753G>T | c.(751-753)gaG>gaT | p.E251D |
| LUAD | 3 | 120876378 | 120876378 | + | Missense_Mutation | SNP | G | G | A | TCGA-49-6761-01A-31D-1945-08 | TCGA-49-6761-11A-01D-1945-08 | g.chr3:120876378G>A | c.781G>A | c.(781-783)Gag>Aag | p.E261K |
| LUAD | 3 | 120876380 | 120876380 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-A491-01A-11D-A24D-08 | TCGA-55-A491-10A-01D-A24F-08 | g.chr3:120876380G>T | c.783G>T | c.(781-783)gaG>gaT | p.E261D |
| LUAD | 3 | 120876382 | 120876382 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z058-01A-01W-0747-08 | TCGA-17-Z058-11A-01W-0747-08 | g.chr3:120876382G>A | c.785G>A | c.(784-786)gGc>gAc | p.G262D |
| LUAD | 3 | 120876387 | 120876387 | + | Missense_Mutation | SNP | C | C | G | TCGA-49-4505-01A-01D-1931-08 | TCGA-49-4505-11A-01D-1265-08 | g.chr3:120876387C>G | c.790C>G | c.(790-792)Cag>Gag | p.Q264E |
| LUAD | 3 | 120941999 | 120941999 | + | Missense_Mutation | SNP | C | C | G | TCGA-99-8032-01A-11D-2238-08 | TCGA-99-8032-10A-01D-2238-08 | g.chr3:120941999C>G | c.1106C>G | c.(1105-1107)cCa>cGa | p.P369R |
| LUAD | 3 | 120957869 | 120957869 | + | Silent | SNP | T | T | A | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr3:120957869T>A | c.1236T>A | c.(1234-1236)gtT>gtA | p.V412V |
| LUAD | 3 | 120957921 | 120957921 | + | Missense_Mutation | SNP | T | T | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr3:120957921T>A | c.1288T>A | c.(1288-1290)Tat>Aat | p.Y430N |
| LUAD | 3 | 120959336 | 120959336 | + | Missense_Mutation | SNP | C | C | G | TCGA-49-6744-01A-11D-1855-08 | TCGA-49-6744-11A-01D-1855-08 | g.chr3:120959336C>G | c.1382C>G | c.(1381-1383)cCa>cGa | p.P461R |
| LUAD | 3 | 120973802 | 120973802 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr3:120973802G>T | c.1502G>T | c.(1501-1503)gGa>gTa | p.G501V |
| LUAD | 3 | 120973837 | 120973837 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-4112-01A-01D-1105-08 | TCGA-44-4112-10A-01D-1458-08 | g.chr3:120973837G>T | c.1537G>T | c.(1537-1539)Gac>Tac | p.D513Y |
| LUAD | 3 | 120973916 | 120973916 | + | Missense_Mutation | SNP | T | T | C | TCGA-44-6778-01A-11D-1855-08 | TCGA-44-6778-10A-01D-1855-08 | g.chr3:120973916T>C | c.1616T>C | c.(1615-1617)aTa>aCa | p.I539T |
| LUAD | 3 | 120976087 | 120976087 | + | Missense_Mutation | SNP | T | T | C | TCGA-91-6836-01A-21D-1855-08 | TCGA-91-6836-11A-01D-1855-08 | g.chr3:120976087T>C | c.1739T>C | c.(1738-1740)cTc>cCc | p.L580P |
| LUAD | 3 | 120976095 | 120976095 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z056-01A-01W-0747-08 | TCGA-17-Z056-11A-01W-0747-08 | g.chr3:120976095C>A | c.1747C>A | c.(1747-1749)Cag>Aag | p.Q583K |
| LUAD | 3 | 120976175 | 120976175 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-44-8120-01A-11D-2238-08 | TCGA-44-8120-10A-01D-2238-08 | g.chr3:120976175C>A | c.1827C>A | c.(1825-1827)tgC>tgA | p.C609* |
| LUAD | 3 | 120998722 | 120998722 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8203-01A-11D-2238-08 | TCGA-55-8203-10A-01D-2238-08 | g.chr3:120998722G>T | c.2029G>T | c.(2029-2031)Ggg>Tgg | p.G677W |
| LUAD | 3 | 120998738 | 120998738 | + | Missense_Mutation | SNP | A | A | G | TCGA-55-8205-01A-11D-2238-08 | TCGA-55-8205-10A-01D-2238-08 | g.chr3:120998738A>G | c.2045A>G | c.(2044-2046)tAt>tGt | p.Y682C |
| LUAD | 3 | 120998777 | 120998777 | + | Missense_Mutation | SNP | C | C | A | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr3:120998777C>A | c.2084C>A | c.(2083-2085)cCt>cAt | p.P695H |
| LUAD | 3 | 120998798 | 120998798 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-67-6217-01A-11D-1753-08 | TCGA-67-6217-10A-01D-1753-08 | g.chr3:120998798delT | c.2105delT | c.(2104-2106)attfs | p.I702fs |
| LUAD | 3 | 121126216 | 121126216 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-38-4626-01A-01D-1553-08 | TCGA-38-4626-11A-01D-1553-08 | g.chr3:121126216delG | c.2786delG | c.(2785-2787)tggfs | p.W929fs |
| LUAD | 3 | 121126217 | 121126217 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr3:121126217G>T | c.2787G>T | c.(2785-2787)tgG>tgT | p.W929C |
| LUAD | 3 | 121126342 | 121126342 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z027-01A-01W-0746-08 | TCGA-17-Z027-11A-01W-0746-08 | g.chr3:121126342T>C | c.2912T>C | c.(2911-2913)gTt>gCt | p.V971A |
| LUAD | 3 | 121134767 | 121134767 | + | Missense_Mutation | SNP | A | A | G | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr3:121134767A>G | c.3250A>G | c.(3250-3252)Aag>Gag | p.K1084E |
| LUAD | 3 | 121137243 | 121137243 | + | Missense_Mutation | SNP | G | G | C | TCGA-50-5941-01A-11D-1753-08 | TCGA-50-5941-10A-01D-1753-08 | g.chr3:121137243G>C | c.3358G>C | c.(3358-3360)Ggt>Cgt | p.G1120R |
| LUAD | 3 | 121137303 | 121137303 | + | Missense_Mutation | SNP | C | C | G | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr3:121137303C>G | c.3418C>G | c.(3418-3420)Cgg>Ggg | p.R1140G |
| LUSC | 3 | 120876471 | 120876471 | + | Missense_Mutation | SNP | C | C | G | TCGA-37-3789-01A-01D-0983-08 | TCGA-37-3789-10A-01D-0983-08 | g.chr3:120876471C>G | c.874C>G | c.(874-876)Cat>Gat | p.H292D |
| LUSC | 3 | 120941900 | 120941900 | + | Missense_Mutation | SNP | G | G | T | TCGA-33-4566-01A-01D-1441-08 | TCGA-33-4566-11A-01D-1441-08 | g.chr3:120941900G>T | c.1007G>T | c.(1006-1008)aGa>aTa | p.R336I |
| LUSC | 3 | 120976075 | 120976075 | + | Missense_Mutation | SNP | C | C | T | TCGA-43-5668-01A-01D-1632-08 | TCGA-43-5668-11A-01D-1632-08 | g.chr3:120976075C>T | c.1727C>T | c.(1726-1728)cCg>cTg | p.P576L |
| LUSC | 3 | 120977893 | 120977893 | + | Silent | SNP | G | G | T | TCGA-46-3769-01A-01D-0983-08 | TCGA-46-3769-10A-01D-0983-08 | g.chr3:120977893G>T | c.1836G>T | c.(1834-1836)gtG>gtT | p.V612V |
| LUSC | 3 | 120977942 | 120977942 | + | Missense_Mutation | SNP | A | A | G | TCGA-66-2788-01A-01D-0983-08 | TCGA-66-2788-11A-01D-0983-08 | g.chr3:120977942A>G | c.1885A>G | c.(1885-1887)Att>Gtt | p.I629V |
| LUSC | 3 | 121100357 | 121100357 | + | Missense_Mutation | SNP | G | G | T | TCGA-18-3415-01A-01D-0983-08 | TCGA-18-3415-11A-01D-0983-08 | g.chr3:121100357G>T | c.2637G>T | c.(2635-2637)gaG>gaT | p.E879D |
| LUSC | 3 | 121126218 | 121126218 | + | Missense_Mutation | SNP | A | A | G | TCGA-85-6560-01A-11D-1817-08 | TCGA-85-6560-10A-01D-1817-08 | g.chr3:121126218A>G | c.2788A>G | c.(2788-2790)Aga>Gga | p.R930G |
| LUSC | 3 | 121137260 | 121137260 | + | Missense_Mutation | SNP | G | G | A | TCGA-33-4547-01A-01D-1267-08 | TCGA-33-4547-11A-01D-1267-08 | g.chr3:121137260G>A | c.3375G>A | c.(3373-3375)atG>atA | p.M1125I |
| LUSC | 3 | 121137266 | 121137266 | + | Silent | SNP | C | C | G | TCGA-60-2713-01A-01D-1522-08 | TCGA-60-2713-11A-01D-1522-08 | g.chr3:121137266C>G | c.3381C>G | c.(3379-3381)ggC>ggG | p.G1127G |
| OV | 3 | 120628437 | 120628437 | + | Silent | SNP | T | T | C | TCGA-23-1120-01A-02W-0484-10 | TCGA-23-1120-10A-01W-0484-10 | g.chr3:120628437T>C | c.12T>C | c.(10-12)ttT>ttC | p.F4F |
| OV | 3 | 120764285 | 120764285 | + | Missense_Mutation | SNP | G | G | T | TCGA-61-2002-01A-01W-0722-08 | TCGA-61-2002-11A-01W-0722-08 | g.chr3:120764285G>T | c.373G>T | c.(373-375)Gcc>Tcc | p.A125S |
| OV | 3 | 120764381 | 120764381 | + | Splice_Site | SNP | C | C | T | TCGA-10-0926-01A-01W-0420-08 | TCGA-10-0926-11A-01D-0399-08 | g.chr3:120764381C>T | c.469C>T | c.(469-471)Cga>Tga | p.R157* |
| OV | 3 | 120957911 | 120957911 | + | Missense_Mutation | SNP | T | T | G | TCGA-24-1423-01A-01W-0545-08 | TCGA-24-1423-10A-01W-0545-08 | g.chr3:120957911T>G | c.1278T>G | c.(1276-1278)atT>atG | p.I426M |
| OV | 3 | 120973862 | 120973862 | + | Missense_Mutation | SNP | A | A | G | TCGA-24-0982-01A-01W-0488-09 | TCGA-24-0982-10C-01W-0488-09 | g.chr3:120973862A>G | c.1562A>G | c.(1561-1563)tAc>tGc | p.Y521C |
| OV | 3 | 120976115 | 120976115 | + | Missense_Mutation | SNP | T | T | A | TCGA-09-2045-01A-01W-0799-08 | TCGA-09-2045-11A-01W-0799-08 | g.chr3:120976115T>A | c.1767T>A | c.(1765-1767)agT>agA | p.S589R |
| OV | 3 | 121137248 | 121137248 | + | Missense_Mutation | SNP | T | T | G | TCGA-13-1489-01A-01W-0549-09 | TCGA-13-1489-10A-01W-0549-09 | g.chr3:121137248T>G | c.3363T>G | c.(3361-3363)agT>agG | p.S1121R |
| PAAD | 3 | 120941850 | 120941850 | + | Splice_Site | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:120941850C>T | c.957C>T | c.(955-957)agC>agT | p.S319S |
| PAAD | 3 | 120957910 | 120957910 | + | Missense_Mutation | SNP | T | T | C | TCGA-LB-A7SX-01A-11D-A33T-08 | TCGA-LB-A7SX-10A-01D-A33W-08 | g.chr3:120957910T>C | c.1277T>C | c.(1276-1278)aTt>aCt | p.I426T |
| PAAD | 3 | 120959317 | 120959317 | + | Missense_Mutation | SNP | C | C | A | TCGA-2J-AAB6-01A-11D-A40W-08 | TCGA-2J-AAB6-10A-01D-A40W-08 | g.chr3:120959317C>A | c.1363C>A | c.(1363-1365)Ctt>Att | p.L455I |
| PAAD | 3 | 120976165 | 120976165 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:120976165G>A | c.1817G>A | c.(1816-1818)aGt>aAt | p.S606N |
| PAAD | 3 | 121097633 | 121097633 | + | Silent | SNP | C | C | T | TCGA-IB-A5SQ-01A-11D-A32N-08 | TCGA-IB-A5SQ-10A-01D-A32N-08 | g.chr3:121097633C>T | c.2319C>T | c.(2317-2319)gcC>gcT | p.A773A |
| PAAD | 3 | 121126092 | 121126092 | + | Missense_Mutation | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:121126092A>G | c.2662A>G | c.(2662-2664)Aca>Gca | p.T888A |
| PAAD | 3 | 121126282 | 121126282 | + | Missense_Mutation | SNP | T | T | C | TCGA-3A-A9IR-01A-11D-A38G-08 | TCGA-3A-A9IR-10A-01D-A38J-08 | g.chr3:121126282T>C | c.2852T>C | c.(2851-2853)aTa>aCa | p.I951T |
| PAAD | 3 | 121126378 | 121126378 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:121126378C>T | c.2948C>T | c.(2947-2949)gCa>gTa | p.A983V |
| PAAD | 3 | 121132069 | 121132069 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:121132069C>T | c.3085C>T | c.(3085-3087)Cga>Tga | p.R1029* |
| PAAD | 3 | 121137938 | 121137938 | + | Missense_Mutation | SNP | A | A | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:121137938A>C | c.3555A>C | c.(3553-3555)caA>caC | p.Q1185H |
| PRAD | 3 | 120871393 | 120871393 | + | Missense_Mutation | SNP | G | G | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:120871393G>T | c.739G>T | c.(739-741)Gtt>Ttt | p.V247F |
| PRAD | 3 | 120969598 | 120969598 | + | Missense_Mutation | SNP | G | G | A | TCGA-EJ-A65D-01A-11D-A30E-08 | TCGA-EJ-A65D-10A-01D-A30H-08 | g.chr3:120969598G>A | c.1429G>A | c.(1429-1431)Gat>Aat | p.D477N |
| PRAD | 3 | 120976076 | 120976076 | + | Silent | SNP | G | G | A | TCGA-YL-A8S9-01A-11D-A377-08 | TCGA-YL-A8S9-10A-01D-A37A-08 | g.chr3:120976076G>A | c.1728G>A | c.(1726-1728)ccG>ccA | p.P576P |
| PRAD | 3 | 120998787 | 120998787 | + | Missense_Mutation | SNP | C | C | A | TCGA-2A-A8VO-01A-11D-A377-08 | TCGA-2A-A8VO-10A-01D-A37A-08 | g.chr3:120998787C>A | c.2094C>A | c.(2092-2094)aaC>aaA | p.N698K |
| PRAD | 3 | 121137219 | 121137219 | + | Missense_Mutation | SNP | C | C | A | TCGA-EJ-5511-01A-01D-1576-08 | TCGA-EJ-5511-10A-01D-1577-08 | g.chr3:121137219C>A | c.3334C>A | c.(3334-3336)Ctt>Att | p.L1112I |
| READ | 3 | 120628436 | 120628436 | + | Missense_Mutation | SNP | T | T | C | TCGA-F5-6702-01A-11D-1826-10 | TCGA-F5-6702-10A-01D-1826-10 | g.chr3:120628436T>C | c.11T>C | c.(10-12)tTt>tCt | p.F4S |
| READ | 3 | 120924773 | 120924773 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:120924773A>C | c.881A>C | c.(880-882)aAa>aCa | p.K294T |
| READ | 3 | 120973920 | 120973920 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:120973920T>G | c.1620T>G | c.(1618-1620)atT>atG | p.I540M |
| READ | 3 | 121097652 | 121097652 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:121097652C>T | c.2338C>T | c.(2338-2340)Cgc>Tgc | p.R780C |
| SARC | 3 | 120840490 | 120840490 | + | Missense_Mutation | SNP | C | C | T | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr3:120840490C>T | c.608C>T | c.(607-609)tCc>tTc | p.S203F |
| SARC | 3 | 120840491 | 120840491 | + | Silent | SNP | C | C | T | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr3:120840491C>T | c.609C>T | c.(607-609)tcC>tcT | p.S203S |
| SARC | 3 | 120941941 | 120941941 | + | Missense_Mutation | SNP | G | G | T | TCGA-FX-A8OO-01A-11D-A36J-09 | TCGA-FX-A8OO-10A-01D-A36M-09 | g.chr3:120941941G>T | c.1048G>T | c.(1048-1050)Gta>Tta | p.V350L |
| SARC | 3 | 121132018 | 121132018 | + | Missense_Mutation | SNP | C | C | T | TCGA-DX-AB32-01A-11D-A417-09 | TCGA-DX-AB32-10A-01D-A41A-09 | g.chr3:121132018C>T | c.3034C>T | c.(3034-3036)Cgc>Tgc | p.R1012C |
| SKCM | 3 | 120628589 | 120628589 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19D-06A-11D-A197-08 | TCGA-ER-A19D-10A-01D-A199-08 | g.chr3:120628589C>T | c.164C>T | c.(163-165)aCt>aTt | p.T55I |
| SKCM | 3 | 120673793 | 120673793 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A42K-06A-11D-A24R-08 | TCGA-ER-A42K-10A-01D-A24R-08 | g.chr3:120673793C>T | c.196C>T | c.(196-198)Cgg>Tgg | p.R66W |
| SKCM | 3 | 120673799 | 120673799 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr3:120673799G>A | c.202G>A | c.(202-204)Ggt>Agt | p.G68S |
| SKCM | 3 | 120673799 | 120673799 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr3:120673799G>A | c.202G>A | c.(202-204)Ggt>Agt | p.G68S |
| SKCM | 3 | 120673835 | 120673835 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chr3:120673835C>T | c.238C>T | c.(238-240)Cca>Tca | p.P80S |
| SKCM | 3 | 120673881 | 120673881 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29R-06A-11D-A197-08 | TCGA-EE-A29R-10A-01D-A199-08 | g.chr3:120673881G>A | c.284G>A | c.(283-285)cGa>cAa | p.R95Q |
| SKCM | 3 | 120673881 | 120673881 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr3:120673881G>A | c.284G>A | c.(283-285)cGa>cAa | p.R95Q |
| SKCM | 3 | 120760550 | 120760550 | + | Silent | SNP | C | C | T | TCGA-FR-A44A-06A-11D-A24R-08 | TCGA-FR-A44A-10A-01D-A24R-08 | g.chr3:120760550C>T | c.291C>T | c.(289-291)ctC>ctT | p.L97L |
| SKCM | 3 | 120760567 | 120760567 | + | Missense_Mutation | SNP | A | A | T | TCGA-D3-A5GR-06A-11D-A27K-08 | TCGA-D3-A5GR-10A-01D-A27N-08 | g.chr3:120760567A>T | c.308A>T | c.(307-309)gAt>gTt | p.D103V |
| SKCM | 3 | 120760584 | 120760584 | + | Missense_Mutation | SNP | G | G | A | TCGA-RP-A694-06A-11D-A30X-08 | TCGA-RP-A694-10A-01D-A30X-08 | g.chr3:120760584G>A | c.325G>A | c.(325-327)Gaa>Aaa | p.E109K |
| SKCM | 3 | 120760603 | 120760603 | + | Missense_Mutation | SNP | T | T | C | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr3:120760603T>C | c.344T>C | c.(343-345)cTa>cCa | p.L115P |
| SKCM | 3 | 120764282 | 120764282 | + | Splice_Site | SNP | G | G | A | TCGA-D3-A5GN-06A-11D-A27K-08 | TCGA-D3-A5GN-10A-01D-A27N-08 | g.chr3:120764282G>A | c.370G>A | c.(370-372)Ggt>Agt | p.G124S |
| SKCM | 3 | 120764302 | 120764302 | + | Missense_Mutation | SNP | T | T | G | TCGA-EE-A2GP-06A-11D-A197-08 | TCGA-EE-A2GP-10A-01D-A199-08 | g.chr3:120764302T>G | c.390T>G | c.(388-390)agT>agG | p.S130R |
| SKCM | 3 | 120764302 | 120764302 | + | Silent | SNP | T | T | C | TCGA-D3-A51N-06A-11D-A25O-08 | TCGA-D3-A51N-10A-01D-A25O-08 | g.chr3:120764302T>C | c.390T>C | c.(388-390)agT>agC | p.S130S |
| SKCM | 3 | 120764309 | 120764309 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:120764309G>A | c.397G>A | c.(397-399)Gat>Aat | p.D133N |
| SKCM | 3 | 120764346 | 120764346 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A4EO-06A-12D-A24R-08 | TCGA-GF-A4EO-10A-01D-A24R-08 | g.chr3:120764346C>T | c.434C>T | c.(433-435)cCa>cTa | p.P145L |
| SKCM | 3 | 120764363 | 120764363 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A1A1-06A-11D-A197-08 | TCGA-ER-A1A1-10A-01D-A199-08 | g.chr3:120764363C>T | c.451C>T | c.(451-453)Ctt>Ttt | p.L151F |
| SKCM | 3 | 120833873 | 120833873 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr3:120833873G>A | c.572G>A | c.(571-573)gGa>gAa | p.G191E |
| SKCM | 3 | 120840528 | 120840528 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2JF-06A-11D-A196-08 | TCGA-D3-A2JF-10A-01D-A198-08 | g.chr3:120840528G>A | c.646G>A | c.(646-648)Gat>Aat | p.D216N |
| SKCM | 3 | 120840528 | 120840528 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A4U4-06A-11D-A32N-08 | TCGA-GN-A4U4-10B-01D-A32N-08 | g.chr3:120840528G>A | c.646G>A | c.(646-648)Gat>Aat | p.D216N |
| SKCM | 3 | 120871407 | 120871407 | + | Splice_Site | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:120871407G>A | c.753G>A | c.(751-753)gaG>gaA | p.E251E |
| SKCM | 3 | 120876350 | 120876350 | + | Splice_Site | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:120876350G>A | | c.e9-1 | |
| SKCM | 3 | 120876375 | 120876375 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr3:120876375C>T | c.778C>T | c.(778-780)Cat>Tat | p.H260Y |
| SKCM | 3 | 120876451 | 120876451 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr3:120876451C>T | c.854C>T | c.(853-855)cCt>cTt | p.P285L |
| SKCM | 3 | 120876453 | 120876453 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A20F-06A-21D-A196-08 | TCGA-EE-A20F-10A-01D-A198-08 | g.chr3:120876453T>A | c.856T>A | c.(856-858)Ttc>Atc | p.F286I |
| SKCM | 3 | 120876460 | 120876460 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AH-06A-11D-A196-08 | TCGA-EE-A3AH-10A-01D-A198-08 | g.chr3:120876460C>T | c.863C>T | c.(862-864)aCc>aTc | p.T288I |
| SKCM | 3 | 120924788 | 120924788 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr3:120924788G>A | c.896G>A | c.(895-897)gGa>gAa | p.G299E |
| SKCM | 3 | 120924811 | 120924811 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr3:120924811C>T | c.919C>T | c.(919-921)Cca>Tca | p.P307S |
| SKCM | 3 | 120924817 | 120924817 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr3:120924817C>T | c.925C>T | c.(925-927)Ctt>Ttt | p.L309F |
| SKCM | 3 | 120924828 | 120924828 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr3:120924828A>T | c.936A>T | c.(934-936)gaA>gaT | p.E312D |
| SKCM | 3 | 120941851 | 120941851 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr3:120941851G>A | c.958G>A | c.(958-960)Gaa>Aaa | p.E320K |
| SKCM | 3 | 120941855 | 120941855 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr3:120941855C>T | c.962C>T | c.(961-963)cCa>cTa | p.P321L |
| SKCM | 3 | 120941953 | 120941953 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A2NH-06A-11D-A196-08 | TCGA-ER-A2NH-10A-01D-A198-08 | g.chr3:120941953G>A | c.1060G>A | c.(1060-1062)Gat>Aat | p.D354N |
| SKCM | 3 | 120941960 | 120941960 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AH-06A-11D-A196-08 | TCGA-EE-A3AH-10A-01D-A198-08 | g.chr3:120941960C>T | c.1067C>T | c.(1066-1068)cCt>cTt | p.P356L |
| SKCM | 3 | 120941994 | 120941994 | + | Silent | SNP | C | C | T | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr3:120941994C>T | c.1101C>T | c.(1099-1101)ccC>ccT | p.P367P |
| SKCM | 3 | 120952497 | 120952497 | + | Silent | SNP | G | G | A | TCGA-EE-A29P-06A-11D-A197-08 | TCGA-EE-A29P-10A-01D-A199-08 | g.chr3:120952497G>A | c.1146G>A | c.(1144-1146)ctG>ctA | p.L382L |
| SKCM | 3 | 120952509 | 120952509 | + | Silent | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr3:120952509C>T | c.1158C>T | c.(1156-1158)ctC>ctT | p.L386L |
| SKCM | 3 | 120952509 | 120952509 | + | Silent | SNP | C | C | T | TCGA-FR-A3YO-06A-11D-A23B-08 | TCGA-FR-A3YO-10A-01D-A23B-08 | g.chr3:120952509C>T | c.1158C>T | c.(1156-1158)ctC>ctT | p.L386L |
| SKCM | 3 | 120957823 | 120957823 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1Q4-06A-11D-A196-08 | TCGA-D3-A1Q4-10A-01D-A198-08 | g.chr3:120957823C>T | c.1190C>T | c.(1189-1191)cCa>cTa | p.P397L |
| SKCM | 3 | 120957823 | 120957823 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GU-06A-11D-A196-08 | TCGA-EE-A2GU-10A-01D-A198-08 | g.chr3:120957823C>T | c.1190C>T | c.(1189-1191)cCa>cTa | p.P397L |
| SKCM | 3 | 120957838 | 120957838 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr3:120957838C>T | c.1205C>T | c.(1204-1206)cCa>cTa | p.P402L |
| SKCM | 3 | 120957858 | 120957858 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr3:120957858G>A | c.1225G>A | c.(1225-1227)Gaa>Aaa | p.E409K |
| SKCM | 3 | 120959317 | 120959317 | + | Missense_Mutation | SNP | C | C | T | TCGA-EB-A5UL-06A-11D-A30X-08 | TCGA-EB-A5UL-10A-01D-A30X-08 | g.chr3:120959317C>T | c.1363C>T | c.(1363-1365)Ctt>Ttt | p.L455F |
| SKCM | 3 | 120969581 | 120969581 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:120969581G>A | c.1412G>A | c.(1411-1413)gGa>gAa | p.G471E |
| SKCM | 3 | 120969584 | 120969584 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:120969584C>T | c.1415C>T | c.(1414-1416)tCa>tTa | p.S472L |
| SKCM | 3 | 120973774 | 120973774 | + | Missense_Mutation | SNP | T | T | G | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr3:120973774T>G | c.1474T>G | c.(1474-1476)Tca>Gca | p.S492A |
| SKCM | 3 | 120973775 | 120973775 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3MV-06A-11D-A21A-08 | TCGA-D3-A3MV-10A-01D-A21A-08 | g.chr3:120973775C>T | c.1475C>T | c.(1474-1476)tCa>tTa | p.S492L |
| SKCM | 3 | 120973808 | 120973808 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr3:120973808G>A | c.1508G>A | c.(1507-1509)gGa>gAa | p.G503E |
| SKCM | 3 | 120973834 | 120973834 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr3:120973834G>A | c.1534G>A | c.(1534-1536)Gaa>Aaa | p.E512K |
| SKCM | 3 | 120973939 | 120973939 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr3:120973939G>A | c.1639G>A | c.(1639-1641)Gaa>Aaa | p.E547K |
| SKCM | 3 | 120976026 | 120976026 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D3-A2JH-06A-11D-A196-08 | TCGA-D3-A2JH-10A-01D-A198-08 | g.chr3:120976026C>T | c.1678C>T | c.(1678-1680)Cag>Tag | p.Q560* |
| SKCM | 3 | 120976071 | 120976071 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr3:120976071C>T | c.1723C>T | c.(1723-1725)Cct>Tct | p.P575S |
| SKCM | 3 | 120976074 | 120976074 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A3F8-06A-11D-A20D-08 | TCGA-DA-A3F8-10A-01D-A20D-08 | g.chr3:120976074C>T | c.1726C>T | c.(1726-1728)Ccg>Tcg | p.P576S |
| SKCM | 3 | 120976086 | 120976086 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19G-06A-11D-A196-08 | TCGA-ER-A19G-10A-01D-A198-08 | g.chr3:120976086C>T | c.1738C>T | c.(1738-1740)Ctc>Ttc | p.L580F |
| SKCM | 3 | 120976108 | 120976108 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr3:120976108C>T | c.1760C>T | c.(1759-1761)tCa>tTa | p.S587L |
| SKCM | 3 | 120976149 | 120976149 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr3:120976149G>A | c.1801G>A | c.(1801-1803)Gga>Aga | p.G601R |
| SKCM | 3 | 120977918 | 120977918 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr3:120977918C>T | c.1861C>T | c.(1861-1863)Cca>Tca | p.P621S |
| SKCM | 3 | 120977920 | 120977920 | + | Silent | SNP | A | A | G | TCGA-GF-A3OT-06A-23D-A23B-08 | TCGA-GF-A3OT-10A-01D-A23B-08 | g.chr3:120977920A>G | c.1863A>G | c.(1861-1863)ccA>ccG | p.P621P |
| SKCM | 3 | 120977927 | 120977927 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D3-A2JA-06A-11D-A196-08 | TCGA-D3-A2JA-10A-01D-A198-08 | g.chr3:120977927C>T | c.1870C>T | c.(1870-1872)Caa>Taa | p.Q624* |
| SKCM | 3 | 120977966 | 120977966 | + | Missense_Mutation | SNP | G | G | A | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr3:120977966G>A | c.1909G>A | c.(1909-1911)Gaa>Aaa | p.E637K |
| SKCM | 3 | 120998689 | 120998689 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr3:120998689G>A | c.1996G>A | c.(1996-1998)Gat>Aat | p.D666N |
| SKCM | 3 | 120998772 | 120998772 | + | Silent | SNP | G | G | A | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr3:120998772G>A | c.2079G>A | c.(2077-2079)cgG>cgA | p.R693R |
| SKCM | 3 | 120998780 | 120998780 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr3:120998780G>A | c.2087G>A | c.(2086-2088)cGa>cAa | p.R696Q |
| SKCM | 3 | 121001140 | 121001140 | + | Missense_Mutation | SNP | A | A | G | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr3:121001140A>G | c.2138A>G | c.(2137-2139)aAc>aGc | p.N713S |
| SKCM | 3 | 121001148 | 121001148 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr3:121001148C>T | c.2146C>T | c.(2146-2148)Cct>Tct | p.P716S |
| SKCM | 3 | 121001148 | 121001148 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AH-06A-11D-A196-08 | TCGA-EE-A3AH-10A-01D-A198-08 | g.chr3:121001148C>T | c.2146C>T | c.(2146-2148)Cct>Tct | p.P716S |
| SKCM | 3 | 121001168 | 121001168 | + | Silent | SNP | C | C | T | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr3:121001168C>T | c.2166C>T | c.(2164-2166)atC>atT | p.I722I |
| SKCM | 3 | 121097679 | 121097679 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr3:121097679C>T | c.2365C>T | c.(2365-2367)Cga>Tga | p.R789* |
| SKCM | 3 | 121097680 | 121097680 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr3:121097680G>A | c.2366G>A | c.(2365-2367)cGa>cAa | p.R789Q |
| SKCM | 3 | 121097730 | 121097730 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr3:121097730G>A | c.2416G>A | c.(2416-2418)Gaa>Aaa | p.E806K |
| SKCM | 3 | 121100148 | 121100148 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr3:121100148G>A | c.2428G>A | c.(2428-2430)Gaa>Aaa | p.E810K |
| SKCM | 3 | 121100150 | 121100150 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr3:121100150A>T | c.2430A>T | c.(2428-2430)gaA>gaT | p.E810D |
| SKCM | 3 | 121100155 | 121100155 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GP-06A-11D-A197-08 | TCGA-EE-A2GP-10A-01D-A199-08 | g.chr3:121100155C>T | c.2435C>T | c.(2434-2436)tCc>tTc | p.S812F |
| SKCM | 3 | 121100155 | 121100155 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1Z0-06A-11D-A197-08 | TCGA-FS-A1Z0-10A-01D-A199-08 | g.chr3:121100155C>T | c.2435C>T | c.(2434-2436)tCc>tTc | p.S812F |
| SKCM | 3 | 121100199 | 121100199 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AF-06A-11D-A196-08 | TCGA-EE-A3AF-10A-01D-A198-08 | g.chr3:121100199G>A | c.2479G>A | c.(2479-2481)Gat>Aat | p.D827N |
| SKCM | 3 | 121100282 | 121100282 | + | Silent | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr3:121100282C>T | c.2562C>T | c.(2560-2562)ttC>ttT | p.F854F |
| SKCM | 3 | 121100318 | 121100318 | + | Silent | SNP | C | C | T | TCGA-D3-A1Q4-06A-11D-A196-08 | TCGA-D3-A1Q4-10A-01D-A198-08 | g.chr3:121100318C>T | c.2598C>T | c.(2596-2598)tcC>tcT | p.S866S |
| SKCM | 3 | 121100379 | 121100379 | + | Splice_Site | SNP | G | G | A | TCGA-FS-A1Z3-06A-11D-A197-08 | TCGA-FS-A1Z3-10A-01D-A199-08 | g.chr3:121100379G>A | c.2659G>A | c.(2659-2661)Ggt>Agt | p.G887S |
| SKCM | 3 | 121126146 | 121126146 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr3:121126146G>A | c.2716G>A | c.(2716-2718)Ggt>Agt | p.G906S |
| SKCM | 3 | 121126203 | 121126203 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr3:121126203A>T | c.2773A>T | c.(2773-2775)Aat>Tat | p.N925Y |
| SKCM | 3 | 121126206 | 121126206 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr3:121126206G>A | c.2776G>A | c.(2776-2778)Gaa>Aaa | p.E926K |
| SKCM | 3 | 121126223 | 121126223 | + | Silent | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr3:121126223G>A | c.2793G>A | c.(2791-2793)agG>agA | p.R931R |
| SKCM | 3 | 121126317 | 121126317 | + | Silent | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr3:121126317C>T | c.2887C>T | c.(2887-2889)Ctg>Ttg | p.L963L |
| SKCM | 3 | 121126335 | 121126335 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr3:121126335C>T | c.2905C>T | c.(2905-2907)Ctt>Ttt | p.L969F |
| SKCM | 3 | 121132123 | 121132123 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr3:121132123G>A | c.3139G>A | c.(3139-3141)Gaa>Aaa | p.E1047K |
| SKCM | 3 | 121137196 | 121137196 | + | Missense_Mutation | SNP | C | C | T | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr3:121137196C>T | c.3311C>T | c.(3310-3312)tCg>tTg | p.S1104L |
| SKCM | 3 | 121137201 | 121137201 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29H-06A-12D-A197-08 | TCGA-EE-A29H-10A-01D-A199-08 | g.chr3:121137201G>A | c.3316G>A | c.(3316-3318)Gga>Aga | p.G1106R |
| SKCM | 3 | 121137202 | 121137202 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr3:121137202G>A | c.3317G>A | c.(3316-3318)gGa>gAa | p.G1106E |
| SKCM | 3 | 121137202 | 121137202 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A3OT-06A-23D-A23B-08 | TCGA-GF-A3OT-10A-01D-A23B-08 | g.chr3:121137202G>A | c.3317G>A | c.(3316-3318)gGa>gAa | p.G1106E |