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 | 2 | 214794743 | 214794743 | + | Missense_Mutation | SNP | A | A | C | TCGA-OR-A5K8-01A-11D-A29I-10 | TCGA-OR-A5K8-10A-01D-A29L-10 | g.chr2:214794743A>C | c.1274A>C | c.(1273-1275)aAa>aCa | p.K425T |
BLCA | 2 | 214149337 | 214149337 | + | Silent | SNP | C | C | T | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr2:214149337C>T | c.130C>T | c.(130-132)Ctg>Ttg | p.L44L |
BLCA | 2 | 214174842 | 214174842 | + | Silent | SNP | C | C | T | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr2:214174842C>T | c.339C>T | c.(337-339)ctC>ctT | p.L113L |
BLCA | 2 | 214204952 | 214204952 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr2:214204952G>A | c.602G>A | c.(601-603)cGa>cAa | p.R201Q |
BLCA | 2 | 214239745 | 214239745 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr2:214239745C>T | c.844C>T | c.(844-846)Cgt>Tgt | p.R282C |
BLCA | 2 | 214794778 | 214794778 | + | Missense_Mutation | SNP | C | C | T | TCGA-5N-A9KI-01A-31D-A42E-08 | TCGA-5N-A9KI-10A-01D-A42H-08 | g.chr2:214794778C>T | c.1309C>T | c.(1309-1311)Cgc>Tgc | p.R437C |
BLCA | 2 | 214794779 | 214794779 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-AAMZ-01A-11D-A42E-08 | TCGA-XF-AAMZ-10A-01D-A42H-08 | g.chr2:214794779G>A | c.1310G>A | c.(1309-1311)cGc>cAc | p.R437H |
BLCA | 2 | 214794833 | 214794833 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-SY-A9G5-01A-11D-A38G-08 | TCGA-SY-A9G5-10A-01D-A38J-08 | g.chr2:214794833C>G | c.1364C>G | c.(1363-1365)tCa>tGa | p.S455* |
BLCA | 2 | 214878727 | 214878727 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9RG-01A-21D-A42E-08 | TCGA-ZF-A9RG-10A-01D-A42H-08 | g.chr2:214878727G>C | c.1453G>C | c.(1453-1455)Gag>Cag | p.E485Q |
BLCA | 2 | 214972961 | 214972961 | + | Silent | SNP | C | C | T | TCGA-FD-A62P-01A-32D-A30E-08 | TCGA-FD-A62P-10A-01D-A30H-08 | g.chr2:214972961C>T | c.1569C>T | c.(1567-1569)atC>atT | p.I523I |
BLCA | 2 | 215274959 | 215274959 | + | Missense_Mutation | SNP | G | G | C | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr2:215274959G>C | c.1816G>C | c.(1816-1818)Gca>Cca | p.A606P |
BLCA | 2 | 215275015 | 215275015 | + | Silent | SNP | C | C | T | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr2:215275015C>T | c.1872C>T | c.(1870-1872)gaC>gaT | p.D624D |
BLCA | 2 | 215275025 | 215275025 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr2:215275025C>T | c.1882C>T | c.(1882-1884)Cga>Tga | p.R628* |
BRCA | 2 | 214149243 | 214149243 | + | Silent | SNP | G | G | C | TCGA-AC-A5XS-01A-11D-A29N-09 | TCGA-AC-A5XS-11A-13D-A29N-09 | g.chr2:214149243G>C | c.36G>C | c.(34-36)gtG>gtC | p.V12V |
BRCA | 2 | 214160797 | 214160797 | + | Missense_Mutation | SNP | T | T | C | TCGA-AR-A251-01A-12D-A167-09 | TCGA-AR-A251-10A-01D-A167-09 | g.chr2:214160797T>C | c.146T>C | c.(145-147)aTa>aCa | p.I49T |
BRCA | 2 | 214160807 | 214160807 | + | Silent | SNP | A | A | T | TCGA-EW-A1PC-01B-11D-A21Q-09 | TCGA-EW-A1PC-10A-01D-A21Q-09 | g.chr2:214160807A>T | c.156A>T | c.(154-156)gcA>gcT | p.A52A |
BRCA | 2 | 214181974 | 214181974 | + | Missense_Mutation | SNP | C | C | T | TCGA-AO-A12E-01A-11D-A10M-09 | TCGA-AO-A12E-10A-01D-A10M-09 | g.chr2:214181974C>T | c.430C>T | c.(430-432)Ctt>Ttt | p.L144F |
BRCA | 2 | 214215282 | 214215282 | + | Silent | SNP | G | G | A | TCGA-BH-A0H7-01A-13W-A071-09 | TCGA-BH-A0H7-11A-13W-A100-09 | g.chr2:214215282G>A | c.675G>A | c.(673-675)ccG>ccA | p.P225P |
BRCA | 2 | 214794711 | 214794711 | + | Silent | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr2:214794711T>G | c.1242T>G | c.(1240-1242)ggT>ggG | p.G414G |
BRCA | 2 | 214878674 | 214878675 | + | Splice_Site | INS | - | - | C | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr2:214878674_214878675insC | | c.e13-1 | |
CESC | 2 | 214354699 | 214354699 | + | Missense_Mutation | SNP | C | C | T | TCGA-FU-A3YQ-01A-11D-A22X-09 | TCGA-FU-A3YQ-10A-01D-A22X-09 | g.chr2:214354699C>T | c.955C>T | c.(955-957)Ccc>Tcc | p.P319S |
CESC | 2 | 214794778 | 214794778 | + | Missense_Mutation | SNP | C | C | T | TCGA-FU-A3TQ-01A-11D-A22X-09 | TCGA-FU-A3TQ-10A-01D-A22X-09 | g.chr2:214794778C>T | c.1309C>T | c.(1309-1311)Cgc>Tgc | p.R437C |
CHOL | 2 | 214794782 | 214794782 | + | Missense_Mutation | SNP | C | C | T | TCGA-4G-AAZT-01A-11D-A417-09 | TCGA-4G-AAZT-10A-01D-A41A-09 | g.chr2:214794782C>T | c.1313C>T | c.(1312-1314)gCa>gTa | p.A438V |
CHOL | 2 | 215275017 | 215275017 | + | Missense_Mutation | SNP | G | G | A | TCGA-4G-AAZO-01A-12D-A417-09 | TCGA-4G-AAZO-11A-11D-A41A-09 | g.chr2:215275017G>A | c.1874G>A | c.(1873-1875)gGc>gAc | p.G625D |
COAD | 2 | 214149312 | 214149312 | + | Silent | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr2:214149312G>A | c.105G>A | c.(103-105)gcG>gcA | p.A35A |
COAD | 2 | 214204963 | 214204964 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr2:214204963_214204964insA | c.613_614insA | c.(613-615)gaafs | p.E205fs |
COAD | 2 | 214215360 | 214215360 | + | Silent | SNP | A | A | C | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:214215360A>C | c.753A>C | c.(751-753)gtA>gtC | p.V251V |
COAD | 2 | 214228854 | 214228854 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6529-01A-11D-1771-10 | TCGA-D5-6529-10A-01D-1771-10 | g.chr2:214228854G>A | c.817G>A | c.(817-819)Ggt>Agt | p.G273S |
COAD | 2 | 214228856 | 214228856 | + | Silent | SNP | T | T | C | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr2:214228856T>C | c.819T>C | c.(817-819)ggT>ggC | p.G273G |
COAD | 2 | 214354773 | 214354773 | + | Silent | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:214354773G>A | c.1029G>A | c.(1027-1029)aaG>aaA | p.K343K |
COAD | 2 | 214354784 | 214354784 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr2:214354784delT | c.1040delT | c.(1039-1041)attfs | p.I347fs |
COAD | 2 | 214794684 | 214794684 | + | Splice_Site | SNP | T | T | C | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr2:214794684T>C | c.1215T>C | c.(1213-1215)agT>agC | p.S405S |
COAD | 2 | 214878766 | 214878766 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:214878766G>A | c.1492G>A | c.(1492-1494)Gca>Aca | p.A498T |
COAD | 2 | 214972925 | 214972925 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr2:214972925A>G | c.1533A>G | c.(1531-1533)atA>atG | p.I511M |
COAD | 2 | 214972975 | 214972975 | + | Missense_Mutation | SNP | T | T | G | TCGA-D5-6932-01A-11D-1924-10 | TCGA-D5-6932-10A-01D-1924-10 | g.chr2:214972975T>G | c.1583T>G | c.(1582-1584)tTt>tGt | p.F528C |
COAD | 2 | 215013920 | 215013920 | + | Silent | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:215013920G>A | c.1650G>A | c.(1648-1650)cgG>cgA | p.R550R |
COAD | 2 | 215274949 | 215274949 | + | Silent | SNP | C | C | T | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr2:215274949C>T | c.1806C>T | c.(1804-1806)caC>caT | p.H602H |
COAD | 2 | 215274978 | 215274978 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chr2:215274978C>A | c.1835C>A | c.(1834-1836)tCt>tAt | p.S612Y |
COAD | 2 | 215275017 | 215275017 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:215275017G>A | c.1874G>A | c.(1873-1875)gGc>gAc | p.G625D |
COAD | 2 | 215275026 | 215275026 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:215275026G>A | c.1883G>A | c.(1882-1884)cGa>cAa | p.R628Q |
COAD | 2 | 215275035 | 215275035 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr2:215275035C>A | c.1892C>A | c.(1891-1893)tCt>tAt | p.S631Y |
COADREAD | 2 | 214149312 | 214149312 | + | Silent | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr2:214149312G>A | c.105G>A | c.(103-105)gcG>gcA | p.A35A |
COADREAD | 2 | 214162055 | 214162055 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:214162055G>T | c.253G>T | c.(253-255)Gaa>Taa | p.E85* |
COADREAD | 2 | 214174838 | 214174838 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr2:214174838T>G | c.335T>G | c.(334-336)tTt>tGt | p.F112C |
COADREAD | 2 | 214204890 | 214204890 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr2:214204890A>C | c.540A>C | c.(538-540)aaA>aaC | p.K180N |
COADREAD | 2 | 214204936 | 214204936 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:214204936C>T | c.586C>T | c.(586-588)Cga>Tga | p.R196* |
COADREAD | 2 | 214204963 | 214204964 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr2:214204963_214204964insA | c.613_614insA | c.(613-615)gaafs | p.E205fs |
COADREAD | 2 | 214215360 | 214215360 | + | Silent | SNP | A | A | C | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:214215360A>C | c.753A>C | c.(751-753)gtA>gtC | p.V251V |
COADREAD | 2 | 214228834 | 214228834 | + | Missense_Mutation | SNP | A | A | G | TCGA-AF-2693-01A-02D-1733-10 | TCGA-AF-2693-10A-01D-1733-10 | g.chr2:214228834A>G | c.797A>G | c.(796-798)cAa>cGa | p.Q266R |
COADREAD | 2 | 214228854 | 214228854 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6529-01A-11D-1771-10 | TCGA-D5-6529-10A-01D-1771-10 | g.chr2:214228854G>A | c.817G>A | c.(817-819)Ggt>Agt | p.G273S |
COADREAD | 2 | 214228856 | 214228856 | + | Silent | SNP | T | T | C | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr2:214228856T>C | c.819T>C | c.(817-819)ggT>ggC | p.G273G |
COADREAD | 2 | 214354773 | 214354773 | + | Silent | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:214354773G>A | c.1029G>A | c.(1027-1029)aaG>aaA | p.K343K |
COADREAD | 2 | 214354784 | 214354784 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr2:214354784delT | c.1040delT | c.(1039-1041)attfs | p.I347fs |
COADREAD | 2 | 214794684 | 214794684 | + | Splice_Site | SNP | T | T | C | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr2:214794684T>C | c.1215T>C | c.(1213-1215)agT>agC | p.S405S |
COADREAD | 2 | 214878766 | 214878766 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:214878766G>A | c.1492G>A | c.(1492-1494)Gca>Aca | p.A498T |
COADREAD | 2 | 214972925 | 214972925 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr2:214972925A>G | c.1533A>G | c.(1531-1533)atA>atG | p.I511M |
COADREAD | 2 | 214972975 | 214972975 | + | Missense_Mutation | SNP | T | T | G | TCGA-D5-6932-01A-11D-1924-10 | TCGA-D5-6932-10A-01D-1924-10 | g.chr2:214972975T>G | c.1583T>G | c.(1582-1584)tTt>tGt | p.F528C |
COADREAD | 2 | 215013920 | 215013920 | + | Silent | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:215013920G>A | c.1650G>A | c.(1648-1650)cgG>cgA | p.R550R |
COADREAD | 2 | 215274949 | 215274949 | + | Silent | SNP | C | C | T | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr2:215274949C>T | c.1806C>T | c.(1804-1806)caC>caT | p.H602H |
COADREAD | 2 | 215274978 | 215274978 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chr2:215274978C>A | c.1835C>A | c.(1834-1836)tCt>tAt | p.S612Y |
COADREAD | 2 | 215274985 | 215274985 | + | Silent | SNP | C | C | T | TCGA-AG-3598-01A-01W-0833-10 | TCGA-AG-3598-10A-01W-0833-10 | g.chr2:215274985C>T | c.1842C>T | c.(1840-1842)gaC>gaT | p.D614D |
COADREAD | 2 | 215275017 | 215275017 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:215275017G>A | c.1874G>A | c.(1873-1875)gGc>gAc | p.G625D |
COADREAD | 2 | 215275026 | 215275026 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:215275026G>A | c.1883G>A | c.(1882-1884)cGa>cAa | p.R628Q |
COADREAD | 2 | 215275035 | 215275035 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr2:215275035C>A | c.1892C>A | c.(1891-1893)tCt>tAt | p.S631Y |
DLBC | 2 | 214160817 | 214160817 | + | Missense_Mutation | SNP | G | G | A | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr2:214160817G>A | c.166G>A | c.(166-168)Gac>Aac | p.D56N |
DLBC | 2 | 214354811 | 214354811 | + | Missense_Mutation | SNP | G | G | A | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr2:214354811G>A | c.1067G>A | c.(1066-1068)aGc>aAc | p.S356N |
DLBC | 2 | 215013915 | 215013915 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-GR-7353-01A-11D-2210-10 | TCGA-GR-7353-10A-01D-2210-10 | g.chr2:215013915delT | c.1645delT | c.(1645-1647)tttfs | p.F549fs |
ESCA | 2 | 214160791 | 214160791 | + | Missense_Mutation | SNP | T | T | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr2:214160791T>A | c.140T>A | c.(139-141)gTc>gAc | p.V47D |
ESCA | 2 | 214354802 | 214354802 | + | Missense_Mutation | SNP | T | T | C | TCGA-ZR-A9CJ-01B-11D-A387-09 | TCGA-ZR-A9CJ-10A-01D-A38A-09 | g.chr2:214354802T>C | c.1058T>C | c.(1057-1059)cTt>cCt | p.L353P |
ESCA | 2 | 215013957 | 215013957 | + | Missense_Mutation | SNP | A | A | C | TCGA-IG-A4QS-01A-11D-A27G-09 | TCGA-IG-A4QS-10A-01D-A27G-09 | g.chr2:215013957A>C | c.1687A>C | c.(1687-1689)Agt>Cgt | p.S563R |
GBM | 2 | 214204919 | 214204919 | + | Missense_Mutation | SNP | A | A | G | TCGA-32-4213-01A-01D-1353-08 | TCGA-32-4213-10A-01D-1353-08 | g.chr2:214204919A>G | c.569A>G | c.(568-570)aAa>aGa | p.K190R |
GBMLGG | 2 | 214204919 | 214204919 | + | Missense_Mutation | SNP | A | A | G | TCGA-32-4213-01A-01D-1353-08 | TCGA-32-4213-10A-01D-1353-08 | g.chr2:214204919A>G | c.569A>G | c.(568-570)aAa>aGa | p.K190R |
GBMLGG | 2 | 214239746 | 214239746 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:214239746G>A | c.845G>A | c.(844-846)cGt>cAt | p.R282H |
HNSC | 2 | 214239796 | 214239796 | + | Missense_Mutation | SNP | G | G | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr2:214239796G>A | c.895G>A | c.(895-897)Gcc>Acc | p.A299T |
HNSC | 2 | 214794821 | 214794821 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-6960-01A-41D-2012-08 | TCGA-CV-6960-10A-01D-2013-08 | g.chr2:214794821T>C | c.1352T>C | c.(1351-1353)gTg>gCg | p.V451A |
HNSC | 2 | 214878680 | 214878680 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-6224-01A-11D-1912-08 | TCGA-CQ-6224-10A-01D-1912-08 | g.chr2:214878680G>A | c.1406G>A | c.(1405-1407)aGa>aAa | p.R469K |
HNSC | 2 | 215013944 | 215013944 | + | Silent | SNP | C | C | T | TCGA-TN-A7HL-01A-11D-A34J-08 | TCGA-TN-A7HL-10A-01D-A34M-08 | g.chr2:215013944C>T | c.1674C>T | c.(1672-1674)atC>atT | p.I558I |
HNSC | 2 | 215013969 | 215013969 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-7071-01A-12D-A30E-08 | TCGA-CQ-7071-10A-01D-A30H-08 | g.chr2:215013969G>A | c.1699G>A | c.(1699-1701)Gag>Aag | p.E567K |
HNSC | 2 | 215274872 | 215274872 | + | Silent | SNP | T | T | C | TCGA-CR-6474-01A-11D-1870-08 | TCGA-CR-6474-10A-01D-1870-08 | g.chr2:215274872T>C | c.1729T>C | c.(1729-1731)Tta>Cta | p.L577L |
HNSC | 2 | 215275038 | 215275038 | + | Nonstop_Mutation | SNP | G | G | C | TCGA-CN-6992-01A-11D-1912-08 | TCGA-CN-6992-10A-01D-1912-08 | g.chr2:215275038G>C | c.1895G>C | c.(1894-1896)tGa>tCa | p.*632S |
KIPAN | 2 | 214161997 | 214161997 | + | Missense_Mutation | SNP | C | C | G | TCGA-DW-7839-01A-11D-2136-08 | TCGA-DW-7839-10A-01D-2136-08 | g.chr2:214161997C>G | c.195C>G | c.(193-195)gaC>gaG | p.D65E |
KIRP | 2 | 214161997 | 214161997 | + | Missense_Mutation | SNP | C | C | G | TCGA-DW-7839-01A-11D-2136-08 | TCGA-DW-7839-10A-01D-2136-08 | g.chr2:214161997C>G | c.195C>G | c.(193-195)gaC>gaG | p.D65E |
LGG | 2 | 214239746 | 214239746 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:214239746G>A | c.845G>A | c.(844-846)cGt>cAt | p.R282H |
LIHC | 2 | 214354720 | 214354720 | + | Missense_Mutation | SNP | C | C | T | TCGA-FV-A4ZQ-01A-11D-A25V-10 | TCGA-FV-A4ZQ-10A-01D-A25V-10 | g.chr2:214354720C>T | c.976C>T | c.(976-978)Cca>Tca | p.P326S |
LIHC | 2 | 214727353 | 214727353 | + | Splice_Site | SNP | G | G | T | TCGA-BW-A5NO-01A-11D-A27I-10 | TCGA-BW-A5NO-10A-01D-A27I-10 | g.chr2:214727353G>T | | c.e11+1 | |
LIHC | 2 | 215274960 | 215274960 | + | Missense_Mutation | SNP | C | C | A | TCGA-HP-A5N0-01A-11D-A28X-10 | TCGA-HP-A5N0-10A-01D-A28X-10 | g.chr2:215274960C>A | c.1817C>A | c.(1816-1818)gCa>gAa | p.A606E |
LUAD | 2 | 214174813 | 214174813 | + | Missense_Mutation | SNP | G | G | T | TCGA-78-7155-01A-11D-2036-08 | TCGA-78-7155-10A-01D-2036-08 | g.chr2:214174813G>T | c.310G>T | c.(310-312)Gca>Tca | p.A104S |
LUAD | 2 | 214204937 | 214204937 | + | Missense_Mutation | SNP | G | G | T | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr2:214204937G>T | c.587G>T | c.(586-588)cGa>cTa | p.R196L |
LUAD | 2 | 214204941 | 214204941 | + | Missense_Mutation | SNP | G | G | T | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr2:214204941G>T | c.591G>T | c.(589-591)atG>atT | p.M197I |
LUAD | 2 | 214215278 | 214215278 | + | Missense_Mutation | SNP | A | A | T | TCGA-05-4420-01A-01D-1265-08 | TCGA-05-4420-10A-01D-1265-08 | g.chr2:214215278A>T | c.671A>T | c.(670-672)gAa>gTa | p.E224V |
LUAD | 2 | 214215336 | 214215336 | + | Silent | SNP | G | G | T | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr2:214215336G>T | c.729G>T | c.(727-729)ctG>ctT | p.L243L |
LUAD | 2 | 214215364 | 214215364 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z022-01A-01W-0746-08 | TCGA-17-Z022-11A-01W-0746-08 | g.chr2:214215364G>T | c.757G>T | c.(757-759)Ggg>Tgg | p.G253W |
LUAD | 2 | 214239765 | 214239765 | + | Silent | SNP | A | A | T | TCGA-99-8025-01A-11D-2238-08 | TCGA-99-8025-10A-01D-2238-08 | g.chr2:214239765A>T | c.864A>T | c.(862-864)ccA>ccT | p.P288P |
LUAD | 2 | 214354687 | 214354687 | + | Splice_Site | SNP | G | G | T | TCGA-50-5946-01A-11D-1753-08 | TCGA-50-5946-10A-01D-1753-08 | g.chr2:214354687G>T | c.943G>T | c.(943-945)Gat>Tat | p.D315Y |
LUAD | 2 | 214354705 | 214354705 | + | Missense_Mutation | SNP | G | G | C | TCGA-49-4486-01A-01D-1265-08 | TCGA-49-4486-11A-01D-1265-08 | g.chr2:214354705G>C | c.961G>C | c.(961-963)Gat>Cat | p.D321H |
LUAD | 2 | 214354753 | 214354753 | + | Missense_Mutation | SNP | C | C | G | TCGA-62-A470-01A-11D-A24D-08 | TCGA-62-A470-10A-01D-A24F-08 | g.chr2:214354753C>G | c.1009C>G | c.(1009-1011)Cca>Gca | p.P337A |
LUAD | 2 | 214727307 | 214727307 | + | Missense_Mutation | SNP | G | G | T | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr2:214727307G>T | c.1169G>T | c.(1168-1170)gGa>gTa | p.G390V |
LUAD | 2 | 214727351 | 214727351 | + | Splice_Site | SNP | A | A | T | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr2:214727351A>T | c.1213A>T | c.(1213-1215)Agt>Tgt | p.S405C |
LUAD | 2 | 214794716 | 214794716 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-A4DG-01A-11D-A24D-08 | TCGA-55-A4DG-10A-01D-A24F-08 | g.chr2:214794716C>A | c.1247C>A | c.(1246-1248)aCt>aAt | p.T416N |
LUAD | 2 | 214794721 | 214794721 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z030-01A-01W-0746-08 | TCGA-17-Z030-11A-01W-0746-08 | g.chr2:214794721G>T | c.1252G>T | c.(1252-1254)Gtt>Ttt | p.V418F |
LUAD | 2 | 214794784 | 214794784 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4432-01A-01D-1265-08 | TCGA-05-4432-10A-01D-1265-08 | g.chr2:214794784G>T | c.1315G>T | c.(1315-1317)Gtg>Ttg | p.V439L |
LUAD | 2 | 214794784 | 214794784 | + | Missense_Mutation | SNP | G | G | T | TCGA-38-4629-01A-02D-1265-08 | TCGA-38-4629-11A-01D-1265-08 | g.chr2:214794784G>T | c.1315G>T | c.(1315-1317)Gtg>Ttg | p.V439L |
LUAD | 2 | 214794788 | 214794788 | + | Missense_Mutation | SNP | G | G | T | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr2:214794788G>T | c.1319G>T | c.(1318-1320)tGg>tTg | p.W440L |
LUAD | 2 | 214878756 | 214878756 | + | Silent | SNP | C | C | A | TCGA-17-Z016-01A-01W-0746-08 | TCGA-17-Z016-11A-01W-0746-08 | g.chr2:214878756C>A | c.1482C>A | c.(1480-1482)ctC>ctA | p.L494L |
LUAD | 2 | 215013863 | 215013863 | + | Splice_Site | SNP | G | G | A | TCGA-55-A48Z-01A-12D-A24P-08 | TCGA-55-A48Z-10A-01D-A24P-08 | g.chr2:215013863G>A | | c.e15-1 | |
LUAD | 2 | 215274880 | 215274880 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5946-01A-11D-1753-08 | TCGA-50-5946-10A-01D-1753-08 | g.chr2:215274880G>T | c.1737G>T | c.(1735-1737)caG>caT | p.Q579H |
LUAD | 2 | 215274887 | 215274887 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-3396-01A-01D-1553-08 | TCGA-44-3396-10A-01D-1265-08 | g.chr2:215274887G>T | c.1744G>T | c.(1744-1746)Ggc>Tgc | p.G582C |
LUAD | 2 | 215274946 | 215274946 | + | Silent | SNP | C | C | A | TCGA-49-4514-01A-21D-1855-08 | TCGA-49-4514-11A-01D-1855-08 | g.chr2:215274946C>A | c.1803C>A | c.(1801-1803)ggC>ggA | p.G601G |
LUSC | 2 | 214181977 | 214181977 | + | Silent | SNP | A | A | C | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr2:214181977A>C | c.433A>C | c.(433-435)Aga>Cga | p.R145R |
LUSC | 2 | 214181983 | 214181983 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr2:214181983G>C | c.439G>C | c.(439-441)Gtt>Ctt | p.V147L |
LUSC | 2 | 214204974 | 214204974 | + | Silent | SNP | A | A | G | TCGA-66-2766-01A-01D-1522-08 | TCGA-66-2766-11A-01D-1522-08 | g.chr2:214204974A>G | c.624A>G | c.(622-624)aaA>aaG | p.K208K |
LUSC | 2 | 214215364 | 214215364 | + | Missense_Mutation | SNP | G | G | T | TCGA-66-2770-01A-01D-1522-08 | TCGA-66-2770-11A-01D-1522-08 | g.chr2:214215364G>T | c.757G>T | c.(757-759)Ggg>Tgg | p.G253W |
LUSC | 2 | 214727276 | 214727276 | + | Missense_Mutation | SNP | G | G | T | TCGA-22-4595-01A-01D-1267-08 | TCGA-22-4595-11A-01D-1267-08 | g.chr2:214727276G>T | c.1138G>T | c.(1138-1140)Ggc>Tgc | p.G380C |
LUSC | 2 | 214794706 | 214794706 | + | Missense_Mutation | SNP | A | A | G | TCGA-43-5668-01A-01D-1632-08 | TCGA-43-5668-11A-01D-1632-08 | g.chr2:214794706A>G | c.1237A>G | c.(1237-1239)Agt>Ggt | p.S413G |
LUSC | 2 | 214794767 | 214794767 | + | Missense_Mutation | SNP | A | A | T | TCGA-21-1081-01A-01D-1521-08 | TCGA-21-1081-10B-01D-1521-08 | g.chr2:214794767A>T | c.1298A>T | c.(1297-1299)gAa>gTa | p.E433V |
LUSC | 2 | 214878777 | 214878777 | + | Silent | SNP | C | C | A | TCGA-66-2759-01A-01D-1522-08 | TCGA-66-2759-11A-01D-1522-08 | g.chr2:214878777C>A | c.1503C>A | c.(1501-1503)acC>acA | p.T501T |
LUSC | 2 | 214878802 | 214878802 | + | Splice_Site | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr2:214878802G>A | | c.e13+1 | |
LUSC | 2 | 215274863 | 215274863 | + | Splice_Site | SNP | G | G | T | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr2:215274863G>T | | c.e16-1 | |
LUSC | 2 | 215274882 | 215274882 | + | Missense_Mutation | SNP | C | C | A | TCGA-34-5231-01A-21D-1817-08 | TCGA-34-5231-10A-01D-1817-08 | g.chr2:215274882C>A | c.1739C>A | c.(1738-1740)gCa>gAa | p.A580E |
OV | 2 | 214228856 | 214228856 | + | Silent | SNP | T | T | C | TCGA-24-0982-01A-01W-0488-09 | TCGA-24-0982-10C-01W-0488-09 | g.chr2:214228856T>C | c.819T>C | c.(817-819)ggT>ggC | p.G273G |
OV | 2 | 214794702 | 214794702 | + | Silent | SNP | T | T | C | TCGA-29-2431-01A-01D-1526-09 | TCGA-29-2431-10A-01D-1526-09 | g.chr2:214794702T>C | c.1233T>C | c.(1231-1233)acT>acC | p.T411T |
PAAD | 2 | 214182035 | 214182035 | + | Missense_Mutation | SNP | A | A | C | TCGA-HZ-A8P1-01A-11D-A377-08 | TCGA-HZ-A8P1-10A-01D-A37A-08 | g.chr2:214182035A>C | c.491A>C | c.(490-492)aAc>aCc | p.N164T |
PAAD | 2 | 214354799 | 214354799 | + | Missense_Mutation | SNP | A | A | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:214354799A>C | c.1055A>C | c.(1054-1056)gAa>gCa | p.E352A |
PRAD | 2 | 214174863 | 214174863 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZG-A8QX-01A-11D-A377-08 | TCGA-ZG-A8QX-10A-01D-A37A-08 | g.chr2:214174863G>C | c.360G>C | c.(358-360)atG>atC | p.M120I |
PRAD | 2 | 214794778 | 214794778 | + | Missense_Mutation | SNP | C | C | T | TCGA-G9-6496-01A-11D-1786-08 | TCGA-G9-6496-10A-01D-1786-08 | g.chr2:214794778C>T | c.1309C>T | c.(1309-1311)Cgc>Tgc | p.R437C |
PRAD | 2 | 214878685 | 214878685 | + | Missense_Mutation | SNP | A | A | G | TCGA-EJ-5509-01A-01D-1576-08 | TCGA-EJ-5509-10A-01D-1577-08 | g.chr2:214878685A>G | c.1411A>G | c.(1411-1413)Aga>Gga | p.R471G |
PRAD | 2 | 215013934 | 215013934 | + | Missense_Mutation | SNP | T | T | G | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr2:215013934T>G | c.1664T>G | c.(1663-1665)aTt>aGt | p.I555S |
PRAD | 2 | 215274874 | 215274874 | + | Silent | SNP | A | A | G | TCGA-V1-A8WL-01A-11D-A377-08 | TCGA-V1-A8WL-10A-01D-A37A-08 | g.chr2:215274874A>G | c.1731A>G | c.(1729-1731)ttA>ttG | p.L577L |
READ | 2 | 214162055 | 214162055 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:214162055G>T | c.253G>T | c.(253-255)Gaa>Taa | p.E85* |
READ | 2 | 214174838 | 214174838 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr2:214174838T>G | c.335T>G | c.(334-336)tTt>tGt | p.F112C |
READ | 2 | 214204890 | 214204890 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr2:214204890A>C | c.540A>C | c.(538-540)aaA>aaC | p.K180N |
READ | 2 | 214204936 | 214204936 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:214204936C>T | c.586C>T | c.(586-588)Cga>Tga | p.R196* |
READ | 2 | 214228834 | 214228834 | + | Missense_Mutation | SNP | A | A | G | TCGA-AF-2693-01A-02D-1733-10 | TCGA-AF-2693-10A-01D-1733-10 | g.chr2:214228834A>G | c.797A>G | c.(796-798)cAa>cGa | p.Q266R |
READ | 2 | 215274985 | 215274985 | + | Silent | SNP | C | C | T | TCGA-AG-3598-01A-01W-0833-10 | TCGA-AG-3598-10A-01W-0833-10 | g.chr2:215274985C>T | c.1842C>T | c.(1840-1842)gaC>gaT | p.D614D |
SKCM | 2 | 214174822 | 214174822 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AD-06A-11D-A196-08 | TCGA-EE-A3AD-10A-01D-A198-08 | g.chr2:214174822G>A | c.319G>A | c.(319-321)Gaa>Aaa | p.E107K |
SKCM | 2 | 214204952 | 214204952 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr2:214204952G>A | c.602G>A | c.(601-603)cGa>cAa | p.R201Q |
SKCM | 2 | 214228839 | 214228839 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:214228839G>A | c.802G>A | c.(802-804)Gga>Aga | p.G268R |
SKCM | 2 | 214239754 | 214239754 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2A5-06A-11D-A197-08 | TCGA-EE-A2A5-10A-01D-A199-08 | g.chr2:214239754G>A | c.853G>A | c.(853-855)Gaa>Aaa | p.E285K |
SKCM | 2 | 214354699 | 214354699 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JN-06A-11D-A196-08 | TCGA-D3-A2JN-10A-01D-A198-08 | g.chr2:214354699C>T | c.955C>T | c.(955-957)Ccc>Tcc | p.P319S |
SKCM | 2 | 214354720 | 214354720 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JA-06A-11D-A196-08 | TCGA-D3-A2JA-10A-01D-A198-08 | g.chr2:214354720C>T | c.976C>T | c.(976-978)Cca>Tca | p.P326S |
SKCM | 2 | 214354720 | 214354720 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:214354720C>T | c.976C>T | c.(976-978)Cca>Tca | p.P326S |
SKCM | 2 | 214354720 | 214354721 | + | Missense_Mutation | DNP | CC | CC | TT | TCGA-FS-A4F0-06A-11D-A24R-08 | TCGA-FS-A4F0-10A-01D-A24R-08 | g.chr2:214354720_214354721CC>TT | c.976_977CC>TT | c.(976-978)CCa>TTa | p.P326L |
SKCM | 2 | 214354721 | 214354721 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:214354721C>T | c.977C>T | c.(976-978)cCa>cTa | p.P326L |
SKCM | 2 | 214727214 | 214727214 | + | Missense_Mutation | SNP | C | C | G | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr2:214727214C>G | c.1076C>G | c.(1075-1077)tCc>tGc | p.S359C |
SKCM | 2 | 214727255 | 214727255 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:214727255G>A | c.1117G>A | c.(1117-1119)Gac>Aac | p.D373N |
SKCM | 2 | 214794732 | 214794732 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FS-A1ZW-06A-12D-A197-08 | TCGA-FS-A1ZW-10A-01D-A199-08 | g.chr2:214794732G>A | c.1263G>A | c.(1261-1263)tgG>tgA | p.W421* |
SKCM | 2 | 214794733 | 214794733 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1Z7-06A-11D-A197-08 | TCGA-FS-A1Z7-10A-01D-A199-08 | g.chr2:214794733G>A | c.1264G>A | c.(1264-1266)Gat>Aat | p.D422N |
SKCM | 2 | 214794769 | 214794769 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J3-06A-11D-A20D-08 | TCGA-EE-A3J3-10A-01D-A20D-08 | g.chr2:214794769G>A | c.1300G>A | c.(1300-1302)Gga>Aga | p.G434R |
SKCM | 2 | 214794828 | 214794828 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:214794828C>T | c.1359C>T | c.(1357-1359)tcC>tcT | p.S453S |
SKCM | 2 | 214794838 | 214794838 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr2:214794838G>A | c.1369G>A | c.(1369-1371)Gat>Aat | p.D457N |
SKCM | 2 | 214878736 | 214878736 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:214878736C>T | c.1462C>T | c.(1462-1464)Cct>Tct | p.P488S |
SKCM | 2 | 214878736 | 214878736 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29N-06A-12D-A197-08 | TCGA-EE-A29N-10A-01D-A199-08 | g.chr2:214878736C>T | c.1462C>T | c.(1462-1464)Cct>Tct | p.P488S |
SKCM | 2 | 214878736 | 214878736 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr2:214878736C>T | c.1462C>T | c.(1462-1464)Cct>Tct | p.P488S |
SKCM | 2 | 214878736 | 214878736 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr2:214878736C>T | c.1462C>T | c.(1462-1464)Cct>Tct | p.P488S |
SKCM | 2 | 214878736 | 214878736 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr2:214878736C>T | c.1462C>T | c.(1462-1464)Cct>Tct | p.P488S |
SKCM | 2 | 214878744 | 214878744 | + | Silent | SNP | C | C | T | TCGA-EB-A5UL-06A-11D-A30X-08 | TCGA-EB-A5UL-10A-01D-A30X-08 | g.chr2:214878744C>T | c.1470C>T | c.(1468-1470)tcC>tcT | p.S490S |
SKCM | 2 | 214972961 | 214972961 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr2:214972961C>T | c.1569C>T | c.(1567-1569)atC>atT | p.I523I |
SKCM | 2 | 215274924 | 215274924 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29X-06A-11D-A196-08 | TCGA-EE-A29X-10A-01D-A198-08 | g.chr2:215274924G>A | c.1781G>A | c.(1780-1782)gGg>gAg | p.G594E |