| 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 | 152382545 | 152382545 | + | Missense_Mutation | SNP | T | T | A | TCGA-OR-A5L6-01A-11D-A29I-10 | TCGA-OR-A5L6-10C-01D-A29L-10 | g.chr2:152382545T>A | c.16985A>T | c.(16984-16986)cAg>cTg | p.Q5662L |
| ACC | 2 | 152484133 | 152484133 | + | Missense_Mutation | SNP | G | G | T | TCGA-OR-A5J8-01A-11D-A29I-10 | TCGA-OR-A5J8-10A-01D-A29L-10 | g.chr2:152484133G>T | c.9318C>A | c.(9316-9318)agC>agA | p.S3106R |
| ACC | 2 | 152499355 | 152499355 | + | Missense_Mutation | SNP | T | T | C | TCGA-OR-A5JK-01A-11D-A29I-10 | TCGA-OR-A5JK-10A-01D-A29L-10 | g.chr2:152499355T>C | c.8189A>G | c.(8188-8190)gAt>gGt | p.D2730G |
| ACC | 2 | 152515607 | 152515607 | + | Missense_Mutation | SNP | G | G | T | TCGA-OR-A5JA-01A-11D-A29I-10 | TCGA-OR-A5JA-10A-01D-A29L-10 | g.chr2:152515607G>T | c.6047C>A | c.(6046-6048)gCa>gAa | p.A2016E |
| ACC | 2 | 152521284 | 152521284 | + | Missense_Mutation | SNP | T | T | C | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr2:152521284T>C | c.5332A>G | c.(5332-5334)Acc>Gcc | p.T1778A |
| ACC | 2 | 152537258 | 152537258 | + | Missense_Mutation | SNP | C | C | A | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr2:152537258C>A | c.3028G>T | c.(3028-3030)Gcc>Tcc | p.A1010S |
| ACC | 2 | 152563490 | 152563490 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr2:152563490C>A | c.1057G>T | c.(1057-1059)Gaa>Taa | p.E353* |
| BLCA | 2 | 152342363 | 152342363 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-GV-A6ZA-01A-12D-A339-08 | TCGA-GV-A6ZA-10A-01D-A339-08 | g.chr2:152342363G>A | c.19921C>T | c.(19921-19923)Caa>Taa | p.Q6641* |
| BLCA | 2 | 152342373 | 152342373 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-AA71-01A-31D-A391-08 | TCGA-DK-AA71-10A-01D-A394-08 | g.chr2:152342373G>C | c.19911C>G | c.(19909-19911)atC>atG | p.I6637M |
| BLCA | 2 | 152346493 | 152346493 | + | Missense_Mutation | SNP | T | T | A | TCGA-XF-A9T6-01A-11D-A42E-08 | TCGA-XF-A9T6-10A-01D-A42H-08 | g.chr2:152346493T>A | c.19828A>T | c.(19828-19830)Act>Tct | p.T6610S |
| BLCA | 2 | 152348641 | 152348641 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-AA56-01A-31D-A391-08 | TCGA-ZF-AA56-10A-01D-A394-08 | g.chr2:152348641C>T | c.19460G>A | c.(19459-19461)cGg>cAg | p.R6487Q |
| BLCA | 2 | 152348672 | 152348672 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-ZF-A9R7-01A-11D-A38G-08 | TCGA-ZF-A9R7-10A-01D-A38J-08 | g.chr2:152348672G>A | c.19429C>T | c.(19429-19431)Cag>Tag | p.Q6477* |
| BLCA | 2 | 152348793 | 152348793 | + | Silent | SNP | C | C | A | TCGA-LC-A66R-01A-41D-A30E-08 | TCGA-LC-A66R-10A-01D-A30H-08 | g.chr2:152348793C>A | c.19308G>T | c.(19306-19308)gtG>gtT | p.V6436V |
| BLCA | 2 | 152348933 | 152348933 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A5BR-01A-11D-A26M-08 | TCGA-FD-A5BR-10A-01D-A26K-08 | g.chr2:152348933G>A | c.19273C>T | c.(19273-19275)Cgg>Tgg | p.R6425W |
| BLCA | 2 | 152349881 | 152349881 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1AB-01A-11D-A13W-08 | TCGA-DK-A1AB-10A-01D-A13W-08 | g.chr2:152349881C>T | c.19183G>A | c.(19183-19185)Gaa>Aaa | p.E6395K |
| BLCA | 2 | 152352870 | 152352870 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-AA6S-01A-21D-A391-08 | TCGA-DK-AA6S-10A-01D-A394-08 | g.chr2:152352870C>G | c.18838G>C | c.(18838-18840)Gaa>Caa | p.E6280Q |
| BLCA | 2 | 152362007 | 152362007 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A2I4-01A-11D-A21A-08 | TCGA-DK-A2I4-10A-01D-A21A-08 | g.chr2:152362007C>G | c.18624G>C | c.(18622-18624)caG>caC | p.Q6208H |
| BLCA | 2 | 152362056 | 152362056 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr2:152362056C>T | c.18575G>A | c.(18574-18576)gGa>gAa | p.G6192E |
| BLCA | 2 | 152369279 | 152369279 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9R7-01A-11D-A38G-08 | TCGA-ZF-A9R7-10A-01D-A38J-08 | g.chr2:152369279G>C | c.18211C>G | c.(18211-18213)Cat>Gat | p.H6071D |
| BLCA | 2 | 152374833 | 152374833 | + | Splice_Site | SNP | A | A | G | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr2:152374833A>G | c.17696T>C | c.(17695-17697)aTa>aCa | p.I5899T |
| BLCA | 2 | 152380907 | 152380907 | + | Missense_Mutation | SNP | C | C | T | TCGA-PQ-A6FI-01A-11D-A31L-08 | TCGA-PQ-A6FI-10A-01D-A31J-08 | g.chr2:152380907C>T | c.17294G>A | c.(17293-17295)cGc>cAc | p.R5765H |
| BLCA | 2 | 152381062 | 152381062 | + | Missense_Mutation | SNP | C | C | G | TCGA-G2-A3IE-01A-11D-A20D-08 | TCGA-G2-A3IE-10A-01D-A20D-08 | g.chr2:152381062C>G | c.17238G>C | c.(17236-17238)aaG>aaC | p.K5746N |
| BLCA | 2 | 152394433 | 152394433 | + | Missense_Mutation | SNP | G | G | A | TCGA-FJ-A3Z7-01A-12D-A23M-08 | TCGA-FJ-A3Z7-10A-01D-A23K-08 | g.chr2:152394433G>A | c.15952C>T | c.(15952-15954)Cgt>Tgt | p.R5318C |
| BLCA | 2 | 152394482 | 152394482 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-HQ-A2OE-01A-11D-A202-08 | TCGA-HQ-A2OE-10A-01D-A202-08 | g.chr2:152394482G>T | c.15903C>A | c.(15901-15903)taC>taA | p.Y5301* |
| BLCA | 2 | 152397312 | 152397312 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A3IS-01A-21D-A21A-08 | TCGA-DK-A3IS-10A-01D-A21A-08 | g.chr2:152397312G>C | c.15583C>G | c.(15583-15585)Ctg>Gtg | p.L5195V |
| BLCA | 2 | 152404175 | 152404175 | + | Silent | SNP | G | G | C | TCGA-XF-A9T8-01A-11D-A391-08 | TCGA-XF-A9T8-10A-01D-A394-08 | g.chr2:152404175G>C | c.15132C>G | c.(15130-15132)gtC>gtG | p.V5044V |
| BLCA | 2 | 152418632 | 152418632 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-XF-A9SI-01A-11D-A391-08 | TCGA-XF-A9SI-10A-01D-A394-08 | g.chr2:152418632G>A | c.13885C>T | c.(13885-13887)Cag>Tag | p.Q4629* |
| BLCA | 2 | 152420146 | 152420146 | + | Missense_Mutation | SNP | G | G | T | TCGA-FD-A5C0-01A-11D-A289-08 | TCGA-FD-A5C0-10A-01D-A289-08 | g.chr2:152420146G>T | c.13564C>A | c.(13564-13566)Ctg>Atg | p.L4522M |
| BLCA | 2 | 152420152 | 152420152 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chr2:152420152G>A | c.13558C>T | c.(13558-13560)Cac>Tac | p.H4520Y |
| BLCA | 2 | 152420419 | 152420419 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-E7-A3Y1-01A-11D-A22Z-08 | TCGA-E7-A3Y1-10A-01D-A22Z-08 | g.chr2:152420419delC | c.13394delG | c.(13393-13395)ggcfs | p.G4465fs |
| BLCA | 2 | 152426865 | 152426865 | + | Silent | SNP | G | G | A | TCGA-ZF-A9R7-01A-11D-A38G-08 | TCGA-ZF-A9R7-10A-01D-A38J-08 | g.chr2:152426865G>A | c.12057C>T | c.(12055-12057)taC>taT | p.Y4019Y |
| BLCA | 2 | 152432241 | 152432241 | + | Missense_Mutation | SNP | G | G | C | TCGA-CF-A47X-01A-31D-A23U-08 | TCGA-CF-A47X-10A-01D-A23U-08 | g.chr2:152432241G>C | c.11878C>G | c.(11878-11880)Ctc>Gtc | p.L3960V |
| BLCA | 2 | 152467029 | 152467029 | + | Splice_Site | SNP | C | C | T | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chr2:152467029C>T | | c.e76+1 | |
| BLCA | 2 | 152468805 | 152468805 | + | Silent | SNP | C | C | G | TCGA-GV-A3JZ-01A-11D-A21A-08 | TCGA-GV-A3JZ-10A-01D-A21A-08 | g.chr2:152468805C>G | c.10971G>C | c.(10969-10971)ctG>ctC | p.L3657L |
| BLCA | 2 | 152468823 | 152468823 | + | Missense_Mutation | SNP | C | C | G | TCGA-FJ-A3ZF-01A-11D-A23M-08 | TCGA-FJ-A3ZF-10A-01D-A23K-08 | g.chr2:152468823C>G | c.10953G>C | c.(10951-10953)aaG>aaC | p.K3651N |
| BLCA | 2 | 152468834 | 152468834 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A3WW-01A-22D-A23M-08 | TCGA-DK-A3WW-10A-01D-A23K-08 | g.chr2:152468834C>G | c.10942G>C | c.(10942-10944)Gag>Cag | p.E3648Q |
| BLCA | 2 | 152470790 | 152470790 | + | Splice_Site | SNP | A | A | G | TCGA-BT-A20R-01A-12D-A16O-08 | TCGA-BT-A20R-11A-11D-A16O-08 | g.chr2:152470790A>G | c.10872T>C | c.(10870-10872)gaT>gaC | p.D3624D |
| BLCA | 2 | 152470907 | 152470907 | + | Silent | SNP | C | C | T | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr2:152470907C>T | c.10755G>A | c.(10753-10755)aaG>aaA | p.K3585K |
| BLCA | 2 | 152470966 | 152470966 | + | Missense_Mutation | SNP | C | C | G | TCGA-KQ-A41S-01A-12D-A339-08 | TCGA-KQ-A41S-10C-01D-A339-08 | g.chr2:152470966C>G | c.10696G>C | c.(10696-10698)Gag>Cag | p.E3566Q |
| BLCA | 2 | 152471030 | 152471030 | + | Silent | SNP | C | C | T | TCGA-2F-A9KR-01A-11D-A38G-08 | TCGA-2F-A9KR-10A-01D-A38J-08 | g.chr2:152471030C>T | c.10632G>A | c.(10630-10632)ccG>ccA | p.P3544P |
| BLCA | 2 | 152474926 | 152474926 | + | Missense_Mutation | SNP | C | C | A | TCGA-UY-A78O-01A-12D-A339-08 | TCGA-UY-A78O-10A-01D-A339-08 | g.chr2:152474926C>A | c.10210G>T | c.(10210-10212)Gtt>Ttt | p.V3404F |
| BLCA | 2 | 152477490 | 152477490 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9SJ-01A-11D-A391-08 | TCGA-XF-A9SJ-10A-01D-A394-08 | g.chr2:152477490C>G | c.9774G>C | c.(9772-9774)ttG>ttC | p.L3258F |
| BLCA | 2 | 152477516 | 152477516 | + | Missense_Mutation | SNP | C | C | G | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr2:152477516C>G | c.9748G>C | c.(9748-9750)Gaa>Caa | p.E3250Q |
| BLCA | 2 | 152484043 | 152484043 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A3B3-01A-12D-A202-08 | TCGA-FD-A3B3-10A-01D-A202-08 | g.chr2:152484043C>G | c.9408G>C | c.(9406-9408)caG>caC | p.Q3136H |
| BLCA | 2 | 152484126 | 152484126 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A3IV-01A-22D-A21A-08 | TCGA-DK-A3IV-10A-01D-A21A-08 | g.chr2:152484126C>T | c.9325G>A | c.(9325-9327)Gac>Aac | p.D3109N |
| BLCA | 2 | 152486108 | 152486108 | + | Missense_Mutation | SNP | C | C | T | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr2:152486108C>T | c.9047G>A | c.(9046-9048)cGa>cAa | p.R3016Q |
| BLCA | 2 | 152487762 | 152487762 | + | Intron | SNP | C | C | T | TCGA-FD-A3SJ-01A-12D-A22Z-08 | TCGA-FD-A3SJ-10A-01D-A22Z-08 | g.chr2:152487762C>T | | | |
| BLCA | 2 | 152490339 | 152490339 | + | Intron | SNP | C | C | A | TCGA-YF-AA3L-01A-11D-A38G-08 | TCGA-YF-AA3L-10A-01D-A38J-08 | g.chr2:152490339C>A | | | |
| BLCA | 2 | 152492771 | 152492771 | + | Intron | SNP | C | C | T | TCGA-BT-A42C-01A-11D-A23M-08 | TCGA-BT-A42C-10A-01D-A23K-08 | g.chr2:152492771C>T | | | |
| BLCA | 2 | 152496415 | 152496415 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr2:152496415G>C | c.8845C>G | c.(8845-8847)Ctg>Gtg | p.L2949V |
| BLCA | 2 | 152496476 | 152496476 | + | Silent | SNP | C | C | T | TCGA-4Z-AA7Q-01A-11D-A391-08 | TCGA-4Z-AA7Q-10A-01D-A394-08 | g.chr2:152496476C>T | c.8784G>A | c.(8782-8784)ttG>ttA | p.L2928L |
| BLCA | 2 | 152496552 | 152496552 | + | Missense_Mutation | SNP | T | T | C | TCGA-UY-A78N-01A-12D-A339-08 | TCGA-UY-A78N-10A-01D-A339-08 | g.chr2:152496552T>C | c.8708A>G | c.(8707-8709)cAg>cGg | p.Q2903R |
| BLCA | 2 | 152496556 | 152496556 | + | Missense_Mutation | SNP | G | G | C | TCGA-BT-A20J-01A-11D-A14W-08 | TCGA-BT-A20J-11A-11D-A14W-08 | g.chr2:152496556G>C | c.8704C>G | c.(8704-8706)Ctc>Gtc | p.L2902V |
| BLCA | 2 | 152506791 | 152506791 | + | Missense_Mutation | SNP | C | C | T | TCGA-S5-A6DX-01A-11D-A31L-08 | TCGA-S5-A6DX-10A-01D-A31J-08 | g.chr2:152506791C>T | c.7330G>A | c.(7330-7332)Gag>Aag | p.E2444K |
| BLCA | 2 | 152512506 | 152512506 | + | Missense_Mutation | SNP | T | T | A | TCGA-XF-A9T3-01A-11D-A42E-08 | TCGA-XF-A9T3-10A-01D-A42H-08 | g.chr2:152512506T>A | c.6527A>T | c.(6526-6528)tAc>tTc | p.Y2176F |
| BLCA | 2 | 152512534 | 152512534 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr2:152512534C>A | c.6499G>T | c.(6499-6501)Gaa>Taa | p.E2167* |
| BLCA | 2 | 152512956 | 152512956 | + | Missense_Mutation | SNP | T | T | C | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr2:152512956T>C | c.6206A>G | c.(6205-6207)gAa>gGa | p.E2069G |
| BLCA | 2 | 152520102 | 152520102 | + | Missense_Mutation | SNP | C | C | T | TCGA-E7-A4IJ-01A-31D-A26M-08 | TCGA-E7-A4IJ-10A-01D-A26K-08 | g.chr2:152520102C>T | c.5723G>A | c.(5722-5724)aGc>aAc | p.S1908N |
| BLCA | 2 | 152520352 | 152520352 | + | Missense_Mutation | SNP | C | C | T | TCGA-GD-A76B-01A-11D-A32B-08 | TCGA-GD-A76B-10A-01D-A329-08 | g.chr2:152520352C>T | c.5473G>A | c.(5473-5475)Gaa>Aaa | p.E1825K |
| BLCA | 2 | 152522654 | 152522654 | + | Missense_Mutation | SNP | C | C | A | TCGA-ZF-A9RC-01A-11D-A38G-08 | TCGA-ZF-A9RC-10A-01D-A38J-08 | g.chr2:152522654C>A | c.4981G>T | c.(4981-4983)Gat>Tat | p.D1661Y |
| BLCA | 2 | 152528918 | 152528918 | + | Missense_Mutation | SNP | C | C | G | TCGA-BT-A2LA-01A-11D-A18F-08 | TCGA-BT-A2LA-11A-11D-A18F-08 | g.chr2:152528918C>G | c.4264G>C | c.(4264-4266)Gag>Cag | p.E1422Q |
| BLCA | 2 | 152528918 | 152528918 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chr2:152528918C>T | c.4264G>A | c.(4264-4266)Gag>Aag | p.E1422K |
| BLCA | 2 | 152529144 | 152529144 | + | Silent | SNP | G | G | A | TCGA-XF-A9T0-01A-11D-A391-08 | TCGA-XF-A9T0-10A-01D-A394-08 | g.chr2:152529144G>A | c.4038C>T | c.(4036-4038)ttC>ttT | p.F1346F |
| BLCA | 2 | 152529166 | 152529166 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-AA4T-01A-11D-A38G-08 | TCGA-ZF-AA4T-10A-01D-A38J-08 | g.chr2:152529166G>A | c.4016C>T | c.(4015-4017)tCa>tTa | p.S1339L |
| BLCA | 2 | 152534599 | 152534599 | + | Missense_Mutation | SNP | T | T | A | TCGA-E7-A97Q-01A-11D-A38G-08 | TCGA-E7-A97Q-10A-01D-A38J-08 | g.chr2:152534599T>A | c.3358A>T | c.(3358-3360)Ata>Tta | p.I1120L |
| BLCA | 2 | 152536298 | 152536298 | + | Silent | SNP | A | A | G | TCGA-BT-A3PK-01A-21D-A21Z-08 | TCGA-BT-A3PK-10A-01D-A21Z-08 | g.chr2:152536298A>G | c.3192T>C | c.(3190-3192)taT>taC | p.Y1064Y |
| BLCA | 2 | 152536438 | 152536438 | + | Missense_Mutation | SNP | G | G | C | TCGA-E7-A6MD-01A-41D-A34U-08 | TCGA-E7-A6MD-10B-01D-A34X-08 | g.chr2:152536438G>C | c.3141C>G | c.(3139-3141)atC>atG | p.I1047M |
| BLCA | 2 | 152536438 | 152536438 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-A9SY-01A-21D-A42E-08 | TCGA-XF-A9SY-10A-01D-A42H-08 | g.chr2:152536438G>C | c.3141C>G | c.(3139-3141)atC>atG | p.I1047M |
| BLCA | 2 | 152543972 | 152543972 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A3B8-01A-31D-A20D-08 | TCGA-FD-A3B8-10A-01D-A20D-08 | g.chr2:152543972C>G | c.2598G>C | c.(2596-2598)aaG>aaC | p.K866N |
| BLCA | 2 | 152553184 | 152553184 | + | Silent | SNP | T | T | C | TCGA-GD-A3OP-01A-21D-A21Z-08 | TCGA-GD-A3OP-10A-01D-A21Z-08 | g.chr2:152553184T>C | c.1536A>G | c.(1534-1536)ctA>ctG | p.L512L |
| BLCA | 2 | 152553691 | 152553691 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chr2:152553691C>T | c.1441G>A | c.(1441-1443)Gca>Aca | p.A481T |
| BLCA | 2 | 152579932 | 152579932 | + | Silent | SNP | C | C | G | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chr2:152579932C>G | c.681G>C | c.(679-681)ctG>ctC | p.L227L |
| BLCA | 2 | 152584365 | 152584365 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-XF-A9T8-01A-11D-A391-08 | TCGA-XF-A9T8-10A-01D-A394-08 | g.chr2:152584365G>T | c.134C>A | c.(133-135)tCa>tAa | p.S45* |
| BLCA | 2 | 152589670 | 152589670 | + | Start_Codon_Del | DEL | T | T | - | TCGA-CF-A47T-01A-11D-A23U-08 | TCGA-CF-A47T-10A-01D-A23U-08 | g.chr2:152589670delT | | | |
| BRCA | 2 | 152350316 | 152350316 | + | Silent | SNP | C | C | T | TCGA-BH-A0W7-01A-11D-A10Y-09 | TCGA-BH-A0W7-10A-01D-A110-09 | g.chr2:152350316C>T | c.19077G>A | c.(19075-19077)gtG>gtA | p.V6359V |
| BRCA | 2 | 152350381 | 152350381 | + | Splice_Site | SNP | C | C | G | TCGA-C8-A12T-01A-11D-A10Y-09 | TCGA-C8-A12T-10A-01D-A110-09 | g.chr2:152350381C>G | c.19012G>C | c.(19012-19014)Gtg>Ctg | p.V6338L |
| BRCA | 2 | 152352825 | 152352825 | + | Missense_Mutation | SNP | C | C | G | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr2:152352825C>G | c.18883G>C | c.(18883-18885)Gag>Cag | p.E6295Q |
| BRCA | 2 | 152362016 | 152362017 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-BH-A0GY-01A-11W-A071-09 | TCGA-BH-A0GY-10A-01W-A071-09 | g.chr2:152362016_152362017delCT | c.18614_18615delAG | c.(18613-18615)aagfs | p.K6205fs |
| BRCA | 2 | 152375530 | 152375532 | + | In_Frame_Del | DEL | CTT | CTT | - | TCGA-A8-A06R-01A-11D-A015-09 | TCGA-A8-A06R-10A-01W-A021-09 | g.chr2:152375530_152375532delCTT | c.17539_17541delAAG | c.(17539-17541)aagdel | p.K5847del |
| BRCA | 2 | 152381061 | 152381061 | + | Missense_Mutation | SNP | T | T | C | TCGA-B6-A0RG-01A-11W-A071-09 | TCGA-B6-A0RG-10A-01W-A071-09 | g.chr2:152381061T>C | c.17239A>G | c.(17239-17241)Aag>Gag | p.K5747E |
| BRCA | 2 | 152384078 | 152384078 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A18F-01A-11D-A12B-09 | TCGA-BH-A18F-11A-22D-A12B-09 | g.chr2:152384078C>T | c.16654G>A | c.(16654-16656)Gaa>Aaa | p.E5552K |
| BRCA | 2 | 152390790 | 152390790 | + | Missense_Mutation | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr2:152390790T>G | c.16253A>C | c.(16252-16254)cAc>cCc | p.H5418P |
| BRCA | 2 | 152394411 | 152394411 | + | Missense_Mutation | SNP | C | C | T | TCGA-A2-A0EV-01A-11W-A050-09 | TCGA-A2-A0EV-10A-01W-A055-09 | g.chr2:152394411C>T | c.15974G>A | c.(15973-15975)cGa>cAa | p.R5325Q |
| BRCA | 2 | 152402429 | 152402429 | + | Silent | SNP | C | C | T | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr2:152402429C>T | c.15447G>A | c.(15445-15447)gtG>gtA | p.V5149V |
| BRCA | 2 | 152402958 | 152402958 | + | Splice_Site | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr2:152402958C>T | | c.e106-1 | |
| BRCA | 2 | 152406191 | 152406191 | + | Missense_Mutation | SNP | G | G | C | TCGA-B6-A0RV-01A-11D-A099-09 | TCGA-B6-A0RV-10A-01D-A099-09 | g.chr2:152406191G>C | c.14905C>G | c.(14905-14907)Cac>Gac | p.H4969D |
| BRCA | 2 | 152409956 | 152409956 | + | Missense_Mutation | SNP | G | G | C | TCGA-D8-A27G-01A-11D-A16D-09 | TCGA-D8-A27G-10A-01D-A16D-09 | g.chr2:152409956G>C | c.14584C>G | c.(14584-14586)Cct>Gct | p.P4862A |
| BRCA | 2 | 152410473 | 152410473 | + | Missense_Mutation | SNP | T | T | C | TCGA-C8-A138-01A-11D-A10Y-09 | TCGA-C8-A138-10A-01D-A110-09 | g.chr2:152410473T>C | c.14392A>G | c.(14392-14394)Atg>Gtg | p.M4798V |
| BRCA | 2 | 152420119 | 152420119 | + | Splice_Site | SNP | C | C | A | TCGA-A2-A04Y-01A-21W-A050-09 | TCGA-A2-A04Y-10A-01W-A055-09 | g.chr2:152420119C>A | | c.e91+1 | |
| BRCA | 2 | 152421652 | 152421652 | + | Missense_Mutation | SNP | T | T | C | TCGA-OL-A5D6-01A-21D-A27P-09 | TCGA-OL-A5D6-10A-01D-A27P-09 | g.chr2:152421652T>C | c.13274A>G | c.(13273-13275)aAa>aGa | p.K4425R |
| BRCA | 2 | 152425880 | 152425880 | + | Missense_Mutation | SNP | A | A | C | TCGA-D8-A145-01A-11D-A10Y-09 | TCGA-D8-A145-10A-01D-A110-09 | g.chr2:152425880A>C | c.12334T>G | c.(12334-12336)Tac>Gac | p.Y4112D |
| BRCA | 2 | 152432783 | 152432783 | + | Missense_Mutation | SNP | G | G | T | TCGA-BH-A0GZ-01A-11W-A071-09 | TCGA-BH-A0GZ-10A-01W-A071-09 | g.chr2:152432783G>T | c.11687C>A | c.(11686-11688)gCc>gAc | p.A3896D |
| BRCA | 2 | 152435922 | 152435922 | + | Intron | SNP | T | T | G | TCGA-A2-A0T5-01A-21D-A099-09 | TCGA-A2-A0T5-10A-01D-A099-09 | g.chr2:152435922T>G | | | |
| BRCA | 2 | 152435968 | 152435968 | + | Intron | SNP | C | C | G | TCGA-EW-A1PB-01A-11D-A142-09 | TCGA-EW-A1PB-10A-01D-A142-09 | g.chr2:152435968C>G | | | |
| BRCA | 2 | 152450704 | 152450704 | + | Intron | SNP | T | T | C | TCGA-D8-A1XK-01A-21D-A14K-09 | TCGA-D8-A1XK-10A-01D-A14K-09 | g.chr2:152450704T>C | | | |
| BRCA | 2 | 152466467 | 152466467 | + | Silent | SNP | C | C | T | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chr2:152466467C>T | c.11457G>A | c.(11455-11457)gtG>gtA | p.V3819V |
| BRCA | 2 | 152466574 | 152466574 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-B6-A0WZ-01A-11D-A10G-09 | TCGA-B6-A0WZ-10A-01D-A10G-09 | g.chr2:152466574C>A | c.11350G>T | c.(11350-11352)Gaa>Taa | p.E3784* |
| BRCA | 2 | 152467080 | 152467080 | + | Missense_Mutation | SNP | C | C | G | TCGA-A2-A0EY-01A-11W-A050-09 | TCGA-A2-A0EY-10A-01W-A055-09 | g.chr2:152467080C>G | c.11239G>C | c.(11239-11241)Gat>Cat | p.D3747H |
| BRCA | 2 | 152467319 | 152467319 | + | Missense_Mutation | SNP | G | G | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr2:152467319G>T | c.11138C>A | c.(11137-11139)cCa>cAa | p.P3713Q |
| BRCA | 2 | 152472569 | 152472569 | + | Silent | SNP | G | G | A | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr2:152472569G>A | c.10507C>T | c.(10507-10509)Ctg>Ttg | p.L3503L |
| BRCA | 2 | 152474912 | 152474912 | + | Missense_Mutation | SNP | C | C | G | TCGA-GM-A2DO-01A-11D-A19Y-09 | TCGA-GM-A2DO-10D-01D-A18P-09 | g.chr2:152474912C>G | c.10224G>C | c.(10222-10224)aaG>aaC | p.K3408N |
| BRCA | 2 | 152483696 | 152483696 | + | Silent | SNP | C | C | T | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chr2:152483696C>T | c.9438G>A | c.(9436-9438)caG>caA | p.Q3146Q |
| BRCA | 2 | 152483718 | 152483718 | + | Splice_Site | SNP | T | T | C | TCGA-D8-A1JI-01A-11D-A13L-09 | TCGA-D8-A1JI-10A-01D-A13O-09 | g.chr2:152483718T>C | c.9416A>G | c.(9415-9417)aAc>aGc | p.N3139S |
| BRCA | 2 | 152483720 | 152483720 | + | Splice_Site | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr2:152483720C>T | | c.e66-1 | |
| BRCA | 2 | 152495886 | 152495886 | + | Intron | SNP | C | C | A | TCGA-AC-A3W6-01A-12D-A228-09 | TCGA-AC-A3W6-10A-01D-A22A-09 | g.chr2:152495886C>A | | | |
| BRCA | 2 | 152499685 | 152499686 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-BH-A0E2-01A-11W-A071-09 | TCGA-BH-A0E2-10A-01W-A071-09 | g.chr2:152499685_152499686insT | c.8138_8139insA | c.(8137-8139)aacfs | p.N2713fs |
| BRCA | 2 | 152500596 | 152500596 | + | Silent | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr2:152500596A>C | c.7692T>G | c.(7690-7692)ggT>ggG | p.G2564G |
| BRCA | 2 | 152501038 | 152501038 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A0E0-01A-11W-A071-09 | TCGA-BH-A0E0-10A-01W-A071-09 | g.chr2:152501038G>A | c.7588C>T | c.(7588-7590)Cct>Tct | p.P2530S |
| BRCA | 2 | 152506758 | 152506758 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-AC-A3W5-01A-11D-A228-09 | TCGA-AC-A3W5-10A-01D-A22A-09 | g.chr2:152506758T>A | c.7363A>T | c.(7363-7365)Aag>Tag | p.K2455* |
| BRCA | 2 | 152506885 | 152506885 | + | Silent | SNP | A | A | G | TCGA-PE-A5DC-01A-12D-A27P-09 | TCGA-PE-A5DC-10A-01D-A27P-09 | g.chr2:152506885A>G | c.7236T>C | c.(7234-7236)taT>taC | p.Y2412Y |
| BRCA | 2 | 152507221 | 152507221 | + | Missense_Mutation | SNP | C | C | G | TCGA-A2-A3XZ-01A-42D-A23C-09 | TCGA-A2-A3XZ-10A-01D-A23C-09 | g.chr2:152507221C>G | c.7094G>C | c.(7093-7095)gGa>gCa | p.G2365A |
| BRCA | 2 | 152507244 | 152507244 | + | Missense_Mutation | SNP | G | G | T | TCGA-AR-A1AH-01A-11D-A12B-09 | TCGA-AR-A1AH-10A-01D-A12B-09 | g.chr2:152507244G>T | c.7071C>A | c.(7069-7071)ttC>ttA | p.F2357L |
| BRCA | 2 | 152520097 | 152520097 | + | Missense_Mutation | SNP | C | C | G | TCGA-C8-A274-01A-11D-A16D-09 | TCGA-C8-A274-10A-01D-A16D-09 | g.chr2:152520097C>G | c.5728G>C | c.(5728-5730)Gaa>Caa | p.E1910Q |
| BRCA | 2 | 152527544 | 152527544 | + | Missense_Mutation | SNP | A | A | T | TCGA-E2-A14R-01A-11D-A10Y-09 | TCGA-E2-A14R-10A-01D-A110-09 | g.chr2:152527544A>T | c.4499T>A | c.(4498-4500)cTa>cAa | p.L1500Q |
| BRCA | 2 | 152531842 | 152531842 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr2:152531842G>C | c.3838C>G | c.(3838-3840)Cag>Gag | p.Q1280E |
| BRCA | 2 | 152534685 | 152534685 | + | Missense_Mutation | SNP | T | T | C | TCGA-EW-A2FS-01A-11D-A17D-09 | TCGA-EW-A2FS-10A-01D-A17D-09 | g.chr2:152534685T>C | c.3272A>G | c.(3271-3273)gAc>gGc | p.D1091G |
| BRCA | 2 | 152541307 | 152541307 | + | Silent | SNP | A | A | G | TCGA-E2-A1IN-01A-11D-A13L-09 | TCGA-E2-A1IN-10A-01D-A188-09 | g.chr2:152541307A>G | c.2820T>C | c.(2818-2820)taT>taC | p.Y940Y |
| BRCA | 2 | 152541344 | 152541344 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-D8-A1XK-01A-21D-A14K-09 | TCGA-D8-A1XK-10A-01D-A14K-09 | g.chr2:152541344delG | c.2783delC | c.(2782-2784)cctfs | p.P928fs |
| BRCA | 2 | 152543948 | 152543948 | + | Silent | SNP | G | G | A | TCGA-D8-A27H-01A-11D-A16D-09 | TCGA-D8-A27H-10A-01D-A16D-09 | g.chr2:152543948G>A | c.2622C>T | c.(2620-2622)gcC>gcT | p.A874A |
| BRCA | 2 | 152544005 | 152544005 | + | Missense_Mutation | SNP | C | C | G | TCGA-BH-A1F8-01A-11D-A13L-09 | TCGA-BH-A1F8-11B-21D-A188-09 | g.chr2:152544005C>G | c.2565G>C | c.(2563-2565)atG>atC | p.M855I |
| BRCA | 2 | 152547256 | 152547256 | + | Silent | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr2:152547256C>T | c.2295G>A | c.(2293-2295)acG>acA | p.T765T |
| BRCA | 2 | 152550949 | 152550949 | + | Splice_Site | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr2:152550949A>C | c.1784T>G | c.(1783-1785)gTg>gGg | p.V595G |
| BRCA | 2 | 152553955 | 152553955 | + | Missense_Mutation | SNP | G | G | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr2:152553955G>T | c.1274C>A | c.(1273-1275)tCc>tAc | p.S425Y |
| BRCA | 2 | 152573967 | 152573967 | + | Missense_Mutation | SNP | A | A | G | TCGA-E2-A1B0-01A-11D-A12Q-09 | TCGA-E2-A1B0-10A-01D-A12Q-09 | g.chr2:152573967A>G | c.785T>C | c.(784-786)aTa>aCa | p.I262T |
| BRCA | 2 | 152580858 | 152580858 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-E9-A1R2-01A-11D-A14G-09 | TCGA-E9-A1R2-10A-01D-A14G-09 | g.chr2:152580858C>T | c.528G>A | c.(526-528)tgG>tgA | p.W176* |
| CESC | 2 | 152348657 | 152348657 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr2:152348657C>A | c.19444G>T | c.(19444-19446)Gaa>Taa | p.E6482* |
| CESC | 2 | 152374864 | 152374864 | + | Missense_Mutation | SNP | G | G | T | TCGA-IR-A3LK-01A-12D-A20U-09 | TCGA-IR-A3LK-10A-01D-A20U-09 | g.chr2:152374864G>T | c.17665C>A | c.(17665-17667)Cac>Aac | p.H5889N |
| CESC | 2 | 152375507 | 152375507 | + | Missense_Mutation | SNP | A | A | T | TCGA-MU-A5YI-01A-11D-A32I-09 | TCGA-MU-A5YI-10A-01D-A32I-09 | g.chr2:152375507A>T | c.17564T>A | c.(17563-17565)gTc>gAc | p.V5855D |
| CESC | 2 | 152375533 | 152375533 | + | Missense_Mutation | SNP | C | C | T | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr2:152375533C>T | c.17538G>A | c.(17536-17538)atG>atA | p.M5846I |
| CESC | 2 | 152375560 | 152375560 | + | Missense_Mutation | SNP | C | C | G | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr2:152375560C>G | c.17511G>C | c.(17509-17511)aaG>aaC | p.K5837N |
| CESC | 2 | 152394431 | 152394431 | + | Silent | SNP | A | A | G | TCGA-LP-A4AW-01A-11D-A243-09 | TCGA-LP-A4AW-10A-01D-A243-09 | g.chr2:152394431A>G | c.15954T>C | c.(15952-15954)cgT>cgC | p.R5318R |
| CESC | 2 | 152409245 | 152409245 | + | Missense_Mutation | SNP | G | G | T | TCGA-Q1-A6DW-01A-11D-A32I-09 | TCGA-Q1-A6DW-10B-01D-A32I-09 | g.chr2:152409245G>T | c.14674C>A | c.(14674-14676)Ctt>Att | p.L4892I |
| CESC | 2 | 152419320 | 152419320 | + | Silent | SNP | C | C | T | TCGA-EK-A2RC-01A-11D-A18J-09 | TCGA-EK-A2RC-10A-01D-A18J-09 | g.chr2:152419320C>T | c.13593G>A | c.(13591-13593)ttG>ttA | p.L4531L |
| CESC | 2 | 152422319 | 152422319 | + | Missense_Mutation | SNP | C | C | G | TCGA-IR-A3LH-01A-21D-A20U-09 | TCGA-IR-A3LH-10A-01D-A20U-09 | g.chr2:152422319C>G | c.13069G>C | c.(13069-13071)Gac>Cac | p.D4357H |
| CESC | 2 | 152426701 | 152426701 | + | Missense_Mutation | SNP | G | G | T | TCGA-LP-A5U2-01A-11D-A28B-09 | TCGA-LP-A5U2-10A-01D-A28E-09 | g.chr2:152426701G>T | c.12221C>A | c.(12220-12222)gCt>gAt | p.A4074D |
| CESC | 2 | 152432303 | 152432303 | + | Missense_Mutation | SNP | C | C | G | TCGA-FU-A3HY-01A-11D-A21Q-09 | TCGA-FU-A3HY-10A-01D-A21Q-09 | g.chr2:152432303C>G | c.11816G>C | c.(11815-11817)aGa>aCa | p.R3939T |
| CESC | 2 | 152436012 | 152436012 | + | Intron | SNP | T | T | G | TCGA-C5-A3HE-01A-21D-A22X-09 | TCGA-C5-A3HE-10A-01D-A22X-09 | g.chr2:152436012T>G | | | |
| CESC | 2 | 152447960 | 152447960 | + | Intron | SNP | G | G | C | TCGA-C5-A2LZ-01A-11D-A20U-09 | TCGA-C5-A2LZ-10B-01D-A20U-09 | g.chr2:152447960G>C | | | |
| CESC | 2 | 152472532 | 152472532 | + | Missense_Mutation | SNP | C | C | G | TCGA-C5-A1BI-01B-11D-A13W-08 | TCGA-C5-A1BI-10A-01D-A13W-08 | g.chr2:152472532C>G | c.10544G>C | c.(10543-10545)aGa>aCa | p.R3515T |
| CESC | 2 | 152472557 | 152472557 | + | Missense_Mutation | SNP | G | G | C | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr2:152472557G>C | c.10519C>G | c.(10519-10521)Cca>Gca | p.P3507A |
| CESC | 2 | 152473963 | 152473963 | + | Missense_Mutation | SNP | C | C | G | TCGA-IR-A3LK-01A-12D-A20U-09 | TCGA-IR-A3LK-10A-01D-A20U-09 | g.chr2:152473963C>G | c.10367G>C | c.(10366-10368)tGg>tCg | p.W3456S |
| CESC | 2 | 152476025 | 152476025 | + | Silent | SNP | G | G | A | TCGA-BI-A0VS-01A-11D-A10S-08 | TCGA-BI-A0VS-10A-01D-A10S-08 | g.chr2:152476025G>A | c.10083C>T | c.(10081-10083)atC>atT | p.I3361I |
| CESC | 2 | 152476075 | 152476075 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-C5-A7CO-01A-11D-A351-09 | TCGA-C5-A7CO-10A-01D-A351-09 | g.chr2:152476075G>A | c.10033C>T | c.(10033-10035)Cag>Tag | p.Q3345* |
| CESC | 2 | 152492755 | 152492755 | + | Intron | SNP | C | C | T | TCGA-IR-A3LK-01A-12D-A20U-09 | TCGA-IR-A3LK-10A-01D-A20U-09 | g.chr2:152492755C>T | | | |
| CESC | 2 | 152499129 | 152499129 | + | Missense_Mutation | SNP | G | G | C | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr2:152499129G>C | c.8332C>G | c.(8332-8334)Cct>Gct | p.P2778A |
| CESC | 2 | 152507262 | 152507262 | + | Missense_Mutation | SNP | C | C | G | TCGA-EK-A2PG-01A-11D-A18J-09 | TCGA-EK-A2PG-10A-01D-A18J-09 | g.chr2:152507262C>G | c.7053G>C | c.(7051-7053)gaG>gaC | p.E2351D |
| CESC | 2 | 152518712 | 152518712 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr2:152518712A>C | c.5907T>G | c.(5905-5907)taT>taG | p.Y1969* |
| CESC | 2 | 152518812 | 152518812 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1BI-01B-11D-A13W-08 | TCGA-C5-A1BI-10A-01D-A13W-08 | g.chr2:152518812C>T | c.5807G>A | c.(5806-5808)gGa>gAa | p.G1936E |
| CESC | 2 | 152524371 | 152524371 | + | Missense_Mutation | SNP | G | G | T | TCGA-EK-A2RB-01A-11D-A18J-09 | TCGA-EK-A2RB-10A-01D-A18J-09 | g.chr2:152524371G>T | c.4666C>A | c.(4666-4668)Cca>Aca | p.P1556T |
| CESC | 2 | 152544883 | 152544883 | + | Missense_Mutation | SNP | C | C | T | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr2:152544883C>T | c.2338G>A | c.(2338-2340)Gag>Aag | p.E780K |
| CESC | 2 | 152547324 | 152547324 | + | Missense_Mutation | SNP | G | G | A | TCGA-UC-A7PF-01A-11D-A351-09 | TCGA-UC-A7PF-11A-31D-A351-09 | g.chr2:152547324G>A | c.2227C>T | c.(2227-2229)Cat>Tat | p.H743Y |
| CESC | 2 | 152580836 | 152580836 | + | Missense_Mutation | SNP | G | G | C | TCGA-EK-A2IP-01A-11D-A17W-09 | TCGA-EK-A2IP-10A-01D-A17W-09 | g.chr2:152580836G>C | c.550C>G | c.(550-552)Ctg>Gtg | p.L184V |
| CESC | 2 | 152581994 | 152581994 | + | Missense_Mutation | SNP | G | G | C | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr2:152581994G>C | c.375C>G | c.(373-375)atC>atG | p.I125M |
| CESC | 2 | 152586147 | 152586147 | + | Silent | SNP | G | G | A | TCGA-C5-A1BF-01B-11D-A13W-08 | TCGA-C5-A1BF-10A-01D-A13W-08 | g.chr2:152586147G>A | c.60C>T | c.(58-60)taC>taT | p.Y20Y |
| CHOL | 2 | 152354773 | 152354773 | + | Intron | SNP | C | C | T | TCGA-4G-AAZO-01A-12D-A417-09 | TCGA-4G-AAZO-11A-11D-A41A-09 | g.chr2:152354773C>T | | | |
| CHOL | 2 | 152384096 | 152384096 | + | Missense_Mutation | SNP | C | C | G | TCGA-ZH-A8Y2-01A-11D-A417-09 | TCGA-ZH-A8Y2-10A-01D-A41A-09 | g.chr2:152384096C>G | c.16636G>C | c.(16636-16638)Gac>Cac | p.D5546H |
| CHOL | 2 | 152426643 | 152426643 | + | Missense_Mutation | SNP | G | G | T | TCGA-ZH-A8Y8-01A-51D-A417-09 | TCGA-ZH-A8Y8-10A-01D-A41A-09 | g.chr2:152426643G>T | c.12279C>A | c.(12277-12279)gaC>gaA | p.D4093E |
| CHOL | 2 | 152547337 | 152547337 | + | Missense_Mutation | SNP | A | A | T | TCGA-4G-AAZO-01A-12D-A417-09 | TCGA-4G-AAZO-11A-11D-A41A-09 | g.chr2:152547337A>T | c.2214T>A | c.(2212-2214)caT>caA | p.H738Q |
| COAD | 2 | 152342281 | 152342281 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-4948-01B-11D-1650-10 | TCGA-CK-4948-10A-01D-1650-10 | g.chr2:152342281G>A | c.20003C>T | c.(20002-20004)gCt>gTt | p.A6668V |
| COAD | 2 | 152342310 | 152342310 | + | Silent | SNP | G | G | A | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr2:152342310G>A | c.19974C>T | c.(19972-19974)acC>acT | p.T6658T |
| COAD | 2 | 152342437 | 152342437 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3952-01A-01W-0995-10 | TCGA-AA-3952-10A-01W-0995-10 | g.chr2:152342437C>T | c.19847G>A | c.(19846-19848)cGt>cAt | p.R6616H |
| COAD | 2 | 152346574 | 152346574 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr2:152346574T>G | c.19747A>C | c.(19747-19749)Acc>Ccc | p.T6583P |
| COAD | 2 | 152346910 | 152346910 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr2:152346910C>T | c.19705G>A | c.(19705-19707)Ggg>Agg | p.G6569R |
| COAD | 2 | 152346910 | 152346910 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6537-01A-11D-1719-10 | TCGA-D5-6537-10A-01D-1719-10 | g.chr2:152346910C>T | c.19705G>A | c.(19705-19707)Ggg>Agg | p.G6569R |
| COAD | 2 | 152346914 | 152346914 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr2:152346914G>T | c.19701C>A | c.(19699-19701)agC>agA | p.S6567R |
| COAD | 2 | 152348274 | 152348274 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152348274C>T | c.19505G>A | c.(19504-19506)cGt>cAt | p.R6502H |
| COAD | 2 | 152348652 | 152348652 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152348652C>T | c.19449G>A | c.(19447-19449)atG>atA | p.M6483I |
| COAD | 2 | 152349890 | 152349890 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-5403-01A-01D-1650-10 | TCGA-AZ-5403-10A-01D-1650-10 | g.chr2:152349890G>A | c.19174C>T | c.(19174-19176)Cgc>Tgc | p.R6392C |
| COAD | 2 | 152350675 | 152350675 | + | Splice_Site | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152350675C>A | c.19011G>T | c.(19009-19011)tcG>tcT | p.S6337S |
| COAD | 2 | 152354774 | 152354774 | + | Intron | SNP | C | C | A | TCGA-A6-6648-01A-11D-1771-10 | TCGA-A6-6648-10A-01D-1771-10 | g.chr2:152354774C>A | | | |
| COAD | 2 | 152362070 | 152362070 | + | Silent | SNP | T | T | C | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr2:152362070T>C | c.18561A>G | c.(18559-18561)gaA>gaG | p.E6187E |
| COAD | 2 | 152362070 | 152362070 | + | Silent | SNP | T | T | C | TCGA-CM-5348-01A-21D-1719-10 | TCGA-CM-5348-10A-01D-1719-10 | g.chr2:152362070T>C | c.18561A>G | c.(18559-18561)gaA>gaG | p.E6187E |
| COAD | 2 | 152362072 | 152362072 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr2:152362072C>A | c.18559G>T | c.(18559-18561)Gaa>Taa | p.E6187* |
| COAD | 2 | 152363468 | 152363468 | + | Silent | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:152363468C>T | c.18408G>A | c.(18406-18408)acG>acA | p.T6136T |
| COAD | 2 | 152371377 | 152371377 | + | Silent | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr2:152371377C>T | c.17868G>A | c.(17866-17868)acG>acA | p.T5956T |
| COAD | 2 | 152374882 | 152374882 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152374882C>T | c.17647G>A | c.(17647-17649)Gat>Aat | p.D5883N |
| COAD | 2 | 152376262 | 152376262 | + | Silent | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152376262G>A | c.17397C>T | c.(17395-17397)ttC>ttT | p.F5799F |
| COAD | 2 | 152376267 | 152376267 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152376267T>G | c.17392A>C | c.(17392-17394)Aat>Cat | p.N5798H |
| COAD | 2 | 152381065 | 152381065 | + | Silent | SNP | G | G | T | TCGA-CK-4948-01B-11D-1650-10 | TCGA-CK-4948-10A-01D-1650-10 | g.chr2:152381065G>T | c.17235C>A | c.(17233-17235)atC>atA | p.I5745I |
| COAD | 2 | 152381066 | 152381066 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5860-01A-01D-1650-10 | TCGA-CM-5860-10A-01D-1650-10 | g.chr2:152381066A>G | c.17234T>C | c.(17233-17235)aTc>aCc | p.I5745T |
| COAD | 2 | 152381115 | 152381115 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152381115C>A | c.17185G>T | c.(17185-17187)Gat>Tat | p.D5729Y |
| COAD | 2 | 152381129 | 152381129 | + | Splice_Site | SNP | A | A | G | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152381129A>G | c.17171T>C | c.(17170-17172)gTc>gCc | p.V5724A |
| COAD | 2 | 152382515 | 152382515 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr2:152382515C>A | c.17015G>T | c.(17014-17016)cGg>cTg | p.R5672L |
| COAD | 2 | 152382515 | 152382515 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr2:152382515C>A | c.17015G>T | c.(17014-17016)cGg>cTg | p.R5672L |
| COAD | 2 | 152382515 | 152382515 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6600-01A-11D-1771-10 | TCGA-AZ-6600-11A-01D-1771-10 | g.chr2:152382515C>A | c.17015G>T | c.(17014-17016)cGg>cTg | p.R5672L |
| COAD | 2 | 152382515 | 152382515 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr2:152382515C>T | c.17015G>A | c.(17014-17016)cGg>cAg | p.R5672Q |
| COAD | 2 | 152382516 | 152382516 | + | Missense_Mutation | SNP | G | G | A | TCGA-DM-A28F-01A-11D-A16V-10 | TCGA-DM-A28F-10A-01D-A16V-10 | g.chr2:152382516G>A | c.17014C>T | c.(17014-17016)Cgg>Tgg | p.R5672W |
| COAD | 2 | 152382516 | 152382516 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6321-01A-11D-1719-10 | TCGA-G4-6321-10A-01D-1720-10 | g.chr2:152382516G>A | c.17014C>T | c.(17014-17016)Cgg>Tgg | p.R5672W |
| COAD | 2 | 152382718 | 152382718 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6654-01A-21D-1835-10 | TCGA-A6-6654-10A-01D-1835-10 | g.chr2:152382718G>A | c.16901C>T | c.(16900-16902)aCg>aTg | p.T5634M |
| COAD | 2 | 152383462 | 152383462 | + | Silent | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr2:152383462G>A | c.16812C>T | c.(16810-16812)ctC>ctT | p.L5604L |
| COAD | 2 | 152390002 | 152390002 | + | Intron | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr2:152390002C>T | | | |
| COAD | 2 | 152390743 | 152390743 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152390743C>T | c.16300G>A | c.(16300-16302)Gac>Aac | p.D5434N |
| COAD | 2 | 152393677 | 152393677 | + | Missense_Mutation | SNP | A | A | T | TCGA-DM-A1DA-01A-11D-A152-10 | TCGA-DM-A1DA-10A-01D-A152-10 | g.chr2:152393677A>T | c.16073T>A | c.(16072-16074)cTg>cAg | p.L5358Q |
| COAD | 2 | 152393704 | 152393704 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-6751-01A-11D-1835-10 | TCGA-CK-6751-10A-01D-1835-10 | g.chr2:152393704T>C | c.16046A>G | c.(16045-16047)tAt>tGt | p.Y5349C |
| COAD | 2 | 152394412 | 152394412 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr2:152394412G>A | c.15973C>T | c.(15973-15975)Cga>Tga | p.R5325* |
| COAD | 2 | 152394477 | 152394477 | + | Missense_Mutation | SNP | T | T | A | TCGA-CK-6747-01A-11D-1835-10 | TCGA-CK-6747-10A-01D-1835-10 | g.chr2:152394477T>A | c.15908A>T | c.(15907-15909)gAg>gTg | p.E5303V |
| COAD | 2 | 152396866 | 152396866 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr2:152396866C>T | c.15781G>A | c.(15781-15783)Gcc>Acc | p.A5261T |
| COAD | 2 | 152397299 | 152397299 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr2:152397299A>G | c.15596T>C | c.(15595-15597)cTt>cCt | p.L5199P |
| COAD | 2 | 152402491 | 152402491 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr2:152402491T>C | c.15385A>G | c.(15385-15387)Aag>Gag | p.K5129E |
| COAD | 2 | 152402870 | 152402870 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3655-01A-02D-1719-10 | TCGA-AA-3655-11A-01D-1719-10 | g.chr2:152402870G>A | c.15352C>T | c.(15352-15354)Cgg>Tgg | p.R5118W |
| COAD | 2 | 152402956 | 152402956 | + | Splice_Site | SNP | A | A | G | TCGA-D5-6529-01A-11D-1771-10 | TCGA-D5-6529-10A-01D-1771-10 | g.chr2:152402956A>G | c.15266T>C | c.(15265-15267)aTt>aCt | p.I5089T |
| COAD | 2 | 152408253 | 152408253 | + | Splice_Site | SNP | G | G | A | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr2:152408253G>A | c.14840C>T | c.(14839-14841)tCg>tTg | p.S4947L |
| COAD | 2 | 152408313 | 152408313 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr2:152408313G>A | c.14780C>T | c.(14779-14781)gCt>gTt | p.A4927V |
| COAD | 2 | 152409185 | 152409185 | + | Splice_Site | SNP | C | C | T | TCGA-CK-5912-01A-11D-1650-10 | TCGA-CK-5912-10A-01D-1650-10 | g.chr2:152409185C>T | | c.e100+1 | |
| COAD | 2 | 152409234 | 152409234 | + | Silent | SNP | A | A | G | TCGA-CM-6168-01A-11D-1650-10 | TCGA-CM-6168-10A-01D-1650-10 | g.chr2:152409234A>G | c.14685T>C | c.(14683-14685)gaT>gaC | p.D4895D |
| COAD | 2 | 152410410 | 152410410 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr2:152410410C>T | c.14455G>A | c.(14455-14457)Gaa>Aaa | p.E4819K |
| COAD | 2 | 152410418 | 152410418 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr2:152410418C>T | c.14447G>A | c.(14446-14448)cGc>cAc | p.R4816H |
| COAD | 2 | 152411488 | 152411488 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr2:152411488G>A | c.14282C>T | c.(14281-14283)cCg>cTg | p.P4761L |
| COAD | 2 | 152417136 | 152417136 | + | Silent | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr2:152417136G>A | c.14181C>T | c.(14179-14181)caC>caT | p.H4727H |
| COAD | 2 | 152417606 | 152417606 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152417606T>C | c.14015A>G | c.(14014-14016)aAt>aGt | p.N4672S |
| COAD | 2 | 152417610 | 152417610 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152417610C>A | c.14011G>T | c.(14011-14013)Gaa>Taa | p.E4671* |
| COAD | 2 | 152421647 | 152421647 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3848-01A-01W-0900-09 | TCGA-AA-3848-10A-01W-0900-09 | g.chr2:152421647T>A | c.13279A>T | c.(13279-13281)Aca>Tca | p.T4427S |
| COAD | 2 | 152421648 | 152421648 | + | Missense_Mutation | SNP | T | T | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152421648T>G | c.13278A>C | c.(13276-13278)gaA>gaC | p.E4426D |
| COAD | 2 | 152423723 | 152423723 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr2:152423723C>T | c.13012G>A | c.(13012-13014)Gat>Aat | p.D4338N |
| COAD | 2 | 152425130 | 152425130 | + | Splice_Site | SNP | A | A | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152425130A>G | | c.e83+1 | |
| COAD | 2 | 152426656 | 152426656 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152426656G>A | c.12266C>T | c.(12265-12267)aCc>aTc | p.T4089I |
| COAD | 2 | 152432753 | 152432753 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3848-01A-01W-0900-09 | TCGA-AA-3848-10A-01W-0900-09 | g.chr2:152432753C>T | c.11717G>A | c.(11716-11718)cGg>cAg | p.R3906Q |
| COAD | 2 | 152432808 | 152432808 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-3810-01A-01W-0995-10 | TCGA-A6-3810-11A-01W-0995-10 | g.chr2:152432808G>A | c.11662C>T | c.(11662-11664)Cct>Tct | p.P3888S |
| COAD | 2 | 152466495 | 152466495 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6607-01A-11D-1835-10 | TCGA-AZ-6607-11A-01D-1835-10 | g.chr2:152466495T>C | c.11429A>G | c.(11428-11430)aAg>aGg | p.K3810R |
| COAD | 2 | 152466553 | 152466553 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152466553A>G | c.11371T>C | c.(11371-11373)Tgt>Cgt | p.C3791R |
| COAD | 2 | 152467090 | 152467090 | + | Silent | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152467090A>G | c.11229T>C | c.(11227-11229)gaT>gaC | p.D3743D |
| COAD | 2 | 152468788 | 152468788 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152468788C>T | c.10988G>A | c.(10987-10989)cGc>cAc | p.R3663H |
| COAD | 2 | 152468789 | 152468789 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152468789G>A | c.10987C>T | c.(10987-10989)Cgc>Tgc | p.R3663C |
| COAD | 2 | 152470797 | 152470797 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6600-01A-11D-1771-10 | TCGA-AZ-6600-11A-01D-1771-10 | g.chr2:152470797T>C | c.10865A>G | c.(10864-10866)cAg>cGg | p.Q3622R |
| COAD | 2 | 152471030 | 152471030 | + | Silent | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152471030C>T | c.10632G>A | c.(10630-10632)ccG>ccA | p.P3544P |
| COAD | 2 | 152471049 | 152471049 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr2:152471049C>A | c.10613G>T | c.(10612-10614)cGg>cTg | p.R3538L |
| COAD | 2 | 152471049 | 152471049 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr2:152471049C>T | c.10613G>A | c.(10612-10614)cGg>cAg | p.R3538Q |
| COAD | 2 | 152471050 | 152471050 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr2:152471050G>A | c.10612C>T | c.(10612-10614)Cgg>Tgg | p.R3538W |
| COAD | 2 | 152471050 | 152471050 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-5348-01A-21D-1719-10 | TCGA-CM-5348-10A-01D-1719-10 | g.chr2:152471050G>A | c.10612C>T | c.(10612-10614)Cgg>Tgg | p.R3538W |
| COAD | 2 | 152476060 | 152476060 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152476060C>T | c.10048G>A | c.(10048-10050)Gat>Aat | p.D3350N |
| COAD | 2 | 152477450 | 152477450 | + | Silent | SNP | G | G | T | TCGA-G4-6299-01A-11D-1771-10 | TCGA-G4-6299-10A-01D-1771-10 | g.chr2:152477450G>T | c.9814C>A | c.(9814-9816)Cgg>Agg | p.R3272R |
| COAD | 2 | 152482051 | 152482051 | + | Silent | SNP | A | A | G | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr2:152482051A>G | c.9720T>C | c.(9718-9720)agT>agC | p.S3240S |
| COAD | 2 | 152482051 | 152482051 | + | Silent | SNP | A | A | G | TCGA-CM-6168-01A-11D-1650-10 | TCGA-CM-6168-10A-01D-1650-10 | g.chr2:152482051A>G | c.9720T>C | c.(9718-9720)agT>agC | p.S3240S |
| COAD | 2 | 152482077 | 152482077 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr2:152482077C>T | c.9694G>A | c.(9694-9696)Gca>Aca | p.A3232T |
| COAD | 2 | 152483635 | 152483635 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr2:152483635C>A | c.9499G>T | c.(9499-9501)Gct>Tct | p.A3167S |
| COAD | 2 | 152484190 | 152484190 | + | Silent | SNP | G | G | A | TCGA-AA-3818-01A-01W-0900-09 | TCGA-AA-3818-10A-01W-0900-09 | g.chr2:152484190G>A | c.9261C>T | c.(9259-9261)agC>agT | p.S3087S |
| COAD | 2 | 152496964 | 152496964 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152496964C>T | c.8590G>A | c.(8590-8592)Gat>Aat | p.D2864N |
| COAD | 2 | 152497158 | 152497158 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152497158C>T | c.8396G>A | c.(8395-8397)cGt>cAt | p.R2799H |
| COAD | 2 | 152500575 | 152500575 | + | Silent | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr2:152500575G>A | c.7713C>T | c.(7711-7713)gaC>gaT | p.D2571D |
| COAD | 2 | 152502711 | 152502711 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr2:152502711T>C | c.7469A>G | c.(7468-7470)cAg>cGg | p.Q2490R |
| COAD | 2 | 152506779 | 152506779 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152506779G>A | c.7342C>T | c.(7342-7344)Cgt>Tgt | p.R2448C |
| COAD | 2 | 152506779 | 152506779 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152506779G>A | c.7342C>T | c.(7342-7344)Cgt>Tgt | p.R2448C |
| COAD | 2 | 152506854 | 152506854 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152506854C>A | c.7267G>T | c.(7267-7269)Gga>Tga | p.G2423* |
| COAD | 2 | 152507181 | 152507181 | + | Silent | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr2:152507181G>A | c.7134C>T | c.(7132-7134)gaC>gaT | p.D2378D |
| COAD | 2 | 152507262 | 152507262 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152507262C>A | c.7053G>T | c.(7051-7053)gaG>gaT | p.E2351D |
| COAD | 2 | 152511795 | 152511795 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152511795G>A | c.6796C>T | c.(6796-6798)Ctg>Ttg | p.L2266L |
| COAD | 2 | 152512665 | 152512665 | + | Splice_Site | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152512665A>G | | c.e49+1 | |
| COAD | 2 | 152512773 | 152512773 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr2:152512773G>A | c.6389C>T | c.(6388-6390)gCc>gTc | p.A2130V |
| COAD | 2 | 152512926 | 152512926 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152512926C>T | c.6236G>A | c.(6235-6237)cGc>cAc | p.R2079H |
| COAD | 2 | 152514562 | 152514562 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr2:152514562A>G | c.6118T>C | c.(6118-6120)Tat>Cat | p.Y2040H |
| COAD | 2 | 152515676 | 152515676 | + | Missense_Mutation | SNP | T | T | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr2:152515676T>A | c.5978A>T | c.(5977-5979)tAc>tTc | p.Y1993F |
| COAD | 2 | 152518781 | 152518781 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152518781C>A | c.5838G>T | c.(5836-5838)gaG>gaT | p.E1946D |
| COAD | 2 | 152520264 | 152520264 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr2:152520264G>A | c.5561C>T | c.(5560-5562)tCa>tTa | p.S1854L |
| COAD | 2 | 152521901 | 152521901 | + | Silent | SNP | G | G | A | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr2:152521901G>A | c.5184C>T | c.(5182-5184)gcC>gcT | p.A1728A |
| COAD | 2 | 152521949 | 152521949 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152521949A>C | c.5136T>G | c.(5134-5136)agT>agG | p.S1712R |
| COAD | 2 | 152521993 | 152521993 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr2:152521993A>G | c.5092T>C | c.(5092-5094)Tcc>Ccc | p.S1698P |
| COAD | 2 | 152522794 | 152522794 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr2:152522794T>C | c.4841A>G | c.(4840-4842)tAc>tGc | p.Y1614C |
| COAD | 2 | 152522864 | 152522864 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152522864G>T | c.4771C>A | c.(4771-4773)Ctc>Atc | p.L1591I |
| COAD | 2 | 152522864 | 152522864 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152522864G>T | c.4771C>A | c.(4771-4773)Ctc>Atc | p.L1591I |
| COAD | 2 | 152527556 | 152527556 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152527556T>C | c.4487A>G | c.(4486-4488)aAc>aGc | p.N1496S |
| COAD | 2 | 152527651 | 152527651 | + | Silent | SNP | G | G | A | TCGA-AA-3837-01A-01W-0900-09 | TCGA-AA-3837-10A-01W-0900-09 | g.chr2:152527651G>A | c.4392C>T | c.(4390-4392)ggC>ggT | p.G1464G |
| COAD | 2 | 152527669 | 152527669 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152527669C>A | c.4374G>T | c.(4372-4374)gaG>gaT | p.E1458D |
| COAD | 2 | 152528901 | 152528901 | + | Silent | SNP | G | G | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr2:152528901G>T | c.4281C>A | c.(4279-4281)gtC>gtA | p.V1427V |
| COAD | 2 | 152528930 | 152528930 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr2:152528930C>T | c.4252G>A | c.(4252-4254)Gcc>Acc | p.A1418T |
| COAD | 2 | 152528931 | 152528931 | + | Silent | SNP | G | G | A | TCGA-D5-6534-01A-21D-1924-10 | TCGA-D5-6534-10A-01D-1924-10 | g.chr2:152528931G>A | c.4251C>T | c.(4249-4251)gaC>gaT | p.D1417D |
| COAD | 2 | 152529066 | 152529066 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152529066C>A | c.4116G>T | c.(4114-4116)aaG>aaT | p.K1372N |
| COAD | 2 | 152529149 | 152529149 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:152529149C>T | c.4033G>A | c.(4033-4035)Ggt>Agt | p.G1345S |
| COAD | 2 | 152534213 | 152534213 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152534213C>T | c.3640G>A | c.(3640-3642)Gaa>Aaa | p.E1214K |
| COAD | 2 | 152534213 | 152534213 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr2:152534213C>T | c.3640G>A | c.(3640-3642)Gaa>Aaa | p.E1214K |
| COAD | 2 | 152534219 | 152534219 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152534219C>T | c.3634G>A | c.(3634-3636)Gac>Aac | p.D1212N |
| COAD | 2 | 152534541 | 152534541 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6606-01A-11D-1835-10 | TCGA-AZ-6606-11A-01D-1835-10 | g.chr2:152534541G>A | c.3416C>T | c.(3415-3417)aCg>aTg | p.T1139M |
| COAD | 2 | 152534587 | 152534587 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152534587G>A | c.3370C>T | c.(3370-3372)Cgg>Tgg | p.R1124W |
| COAD | 2 | 152536255 | 152536255 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr2:152536255C>A | c.3235G>T | c.(3235-3237)Gcc>Tcc | p.A1079S |
| COAD | 2 | 152536488 | 152536488 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr2:152536488G>A | c.3091C>T | c.(3091-3093)Cca>Tca | p.P1031S |
| COAD | 2 | 152541326 | 152541326 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152541326T>C | c.2801A>G | c.(2800-2802)gAc>gGc | p.D934G |
| COAD | 2 | 152541391 | 152541391 | + | Silent | SNP | G | G | A | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr2:152541391G>A | c.2736C>T | c.(2734-2736)gcC>gcT | p.A912A |
| COAD | 2 | 152541479 | 152541479 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152541479C>T | c.2648G>A | c.(2647-2649)cGa>cAa | p.R883Q |
| COAD | 2 | 152543972 | 152543972 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr2:152543972C>A | c.2598G>T | c.(2596-2598)aaG>aaT | p.K866N |
| COAD | 2 | 152544143 | 152544143 | + | Silent | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr2:152544143G>A | c.2520C>T | c.(2518-2520)agC>agT | p.S840S |
| COAD | 2 | 152544209 | 152544209 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152544209C>A | c.2454G>T | c.(2452-2454)aaG>aaT | p.K818N |
| COAD | 2 | 152544228 | 152544228 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr2:152544228C>A | c.2435G>T | c.(2434-2436)tGg>tTg | p.W812L |
| COAD | 2 | 152548407 | 152548407 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152548407C>A | c.2182G>T | c.(2182-2184)Gca>Tca | p.A728S |
| COAD | 2 | 152548416 | 152548416 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152548416C>T | c.2173G>A | c.(2173-2175)Gaa>Aaa | p.E725K |
| COAD | 2 | 152548637 | 152548637 | + | Missense_Mutation | SNP | T | T | A | TCGA-DM-A1D7-01A-11D-A152-10 | TCGA-DM-A1D7-10A-01D-A152-10 | g.chr2:152548637T>A | c.2042A>T | c.(2041-2043)tAt>tTt | p.Y681F |
| COAD | 2 | 152548665 | 152548665 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152548665A>C | c.2014T>G | c.(2014-2016)Tta>Gta | p.L672V |
| COAD | 2 | 152548665 | 152548665 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152548665A>C | c.2014T>G | c.(2014-2016)Tta>Gta | p.L672V |
| COAD | 2 | 152548870 | 152548870 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152548870A>G | c.1903T>C | c.(1903-1905)Tac>Cac | p.Y635H |
| COAD | 2 | 152550884 | 152550884 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152550884C>T | c.1849G>A | c.(1849-1851)Gat>Aat | p.D617N |
| COAD | 2 | 152550885 | 152550885 | + | Silent | SNP | G | G | A | TCGA-A6-5657-01A-01D-1650-10 | TCGA-A6-5657-10A-01D-1650-10 | g.chr2:152550885G>A | c.1848C>T | c.(1846-1848)gaC>gaT | p.D616D |
| COAD | 2 | 152550899 | 152550899 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr2:152550899G>A | c.1834C>T | c.(1834-1836)Ctc>Ttc | p.L612F |
| COAD | 2 | 152550922 | 152550922 | + | Missense_Mutation | SNP | T | T | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152550922T>G | c.1811A>C | c.(1810-1812)aAc>aCc | p.N604T |
| COAD | 2 | 152550935 | 152550935 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152550935C>A | c.1798G>T | c.(1798-1800)Gac>Tac | p.D600Y |
| COAD | 2 | 152552108 | 152552108 | + | Missense_Mutation | SNP | G | G | A | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr2:152552108G>A | c.1658C>T | c.(1657-1659)gCc>gTc | p.A553V |
| COAD | 2 | 152552144 | 152552144 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr2:152552144delG | c.1622delC | c.(1621-1623)cctfs | p.P541fs |
| COAD | 2 | 152552161 | 152552161 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr2:152552161G>T | c.1605C>A | c.(1603-1605)ttC>ttA | p.F535L |
| COAD | 2 | 152563485 | 152563485 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152563485C>A | c.1062G>T | c.(1060-1062)aaG>aaT | p.K354N |
| COAD | 2 | 152579948 | 152579948 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152579948T>G | c.665A>C | c.(664-666)aAt>aCt | p.N222T |
| COAD | 2 | 152580800 | 152580800 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr2:152580800C>T | c.586G>A | c.(586-588)Gtt>Att | p.V196I |
| COAD | 2 | 152582036 | 152582036 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr2:152582036C>A | c.333G>T | c.(331-333)caG>caT | p.Q111H |
| COAD | 2 | 152582046 | 152582046 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr2:152582046G>A | c.323C>T | c.(322-324)aCa>aTa | p.T108I |
| COAD | 2 | 152582047 | 152582047 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3712-01A-21D-1719-10 | TCGA-AA-3712-11A-01D-1719-10 | g.chr2:152582047T>C | c.322A>G | c.(322-324)Aca>Gca | p.T108A |
| COAD | 2 | 152584337 | 152584337 | + | Silent | SNP | C | C | T | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr2:152584337C>T | c.162G>A | c.(160-162)caG>caA | p.Q54Q |
| COAD | 2 | 152589659 | 152589659 | + | Silent | SNP | G | G | A | TCGA-G4-6303-01A-11D-1771-10 | TCGA-G4-6303-10A-01D-1771-10 | g.chr2:152589659G>A | c.12C>T | c.(10-12)gaC>gaT | p.D4D |
| COADREAD | 2 | 152342281 | 152342281 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-4948-01B-11D-1650-10 | TCGA-CK-4948-10A-01D-1650-10 | g.chr2:152342281G>A | c.20003C>T | c.(20002-20004)gCt>gTt | p.A6668V |
| COADREAD | 2 | 152342310 | 152342310 | + | Silent | SNP | G | G | A | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr2:152342310G>A | c.19974C>T | c.(19972-19974)acC>acT | p.T6658T |
| COADREAD | 2 | 152342437 | 152342437 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3952-01A-01W-0995-10 | TCGA-AA-3952-10A-01W-0995-10 | g.chr2:152342437C>T | c.19847G>A | c.(19846-19848)cGt>cAt | p.R6616H |
| COADREAD | 2 | 152346574 | 152346574 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr2:152346574T>G | c.19747A>C | c.(19747-19749)Acc>Ccc | p.T6583P |
| COADREAD | 2 | 152346910 | 152346910 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr2:152346910C>T | c.19705G>A | c.(19705-19707)Ggg>Agg | p.G6569R |
| COADREAD | 2 | 152346910 | 152346910 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6537-01A-11D-1719-10 | TCGA-D5-6537-10A-01D-1719-10 | g.chr2:152346910C>T | c.19705G>A | c.(19705-19707)Ggg>Agg | p.G6569R |
| COADREAD | 2 | 152346914 | 152346914 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr2:152346914G>T | c.19701C>A | c.(19699-19701)agC>agA | p.S6567R |
| COADREAD | 2 | 152348274 | 152348274 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152348274C>T | c.19505G>A | c.(19504-19506)cGt>cAt | p.R6502H |
| COADREAD | 2 | 152348652 | 152348652 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152348652C>T | c.19449G>A | c.(19447-19449)atG>atA | p.M6483I |
| COADREAD | 2 | 152349881 | 152349881 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152349881C>A | c.19183G>T | c.(19183-19185)Gaa>Taa | p.E6395* |
| COADREAD | 2 | 152349890 | 152349890 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-5403-01A-01D-1650-10 | TCGA-AZ-5403-10A-01D-1650-10 | g.chr2:152349890G>A | c.19174C>T | c.(19174-19176)Cgc>Tgc | p.R6392C |
| COADREAD | 2 | 152350675 | 152350675 | + | Splice_Site | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152350675C>A | c.19011G>T | c.(19009-19011)tcG>tcT | p.S6337S |
| COADREAD | 2 | 152350697 | 152350697 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152350697C>T | c.18989G>A | c.(18988-18990)cGc>cAc | p.R6330H |
| COADREAD | 2 | 152354774 | 152354774 | + | Intron | SNP | C | C | A | TCGA-A6-6648-01A-11D-1771-10 | TCGA-A6-6648-10A-01D-1771-10 | g.chr2:152354774C>A | | | |
| COADREAD | 2 | 152359931 | 152359931 | + | Missense_Mutation | SNP | T | T | C | TCGA-AF-6672-01A-11D-1826-10 | TCGA-AF-6672-10A-01D-1826-10 | g.chr2:152359931T>C | c.18664A>G | c.(18664-18666)Aca>Gca | p.T6222A |
| COADREAD | 2 | 152362070 | 152362070 | + | Silent | SNP | T | T | C | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr2:152362070T>C | c.18561A>G | c.(18559-18561)gaA>gaG | p.E6187E |
| COADREAD | 2 | 152362070 | 152362070 | + | Silent | SNP | T | T | C | TCGA-CM-5348-01A-21D-1719-10 | TCGA-CM-5348-10A-01D-1719-10 | g.chr2:152362070T>C | c.18561A>G | c.(18559-18561)gaA>gaG | p.E6187E |
| COADREAD | 2 | 152362072 | 152362072 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr2:152362072C>A | c.18559G>T | c.(18559-18561)Gaa>Taa | p.E6187* |
| COADREAD | 2 | 152363468 | 152363468 | + | Silent | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:152363468C>T | c.18408G>A | c.(18406-18408)acG>acA | p.T6136T |
| COADREAD | 2 | 152371377 | 152371377 | + | Silent | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr2:152371377C>T | c.17868G>A | c.(17866-17868)acG>acA | p.T5956T |
| COADREAD | 2 | 152374882 | 152374882 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152374882C>T | c.17647G>A | c.(17647-17649)Gat>Aat | p.D5883N |
| COADREAD | 2 | 152375525 | 152375525 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152375525G>T | c.17546C>A | c.(17545-17547)tCt>tAt | p.S5849Y |
| COADREAD | 2 | 152376261 | 152376261 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152376261C>T | c.17398G>A | c.(17398-17400)Gat>Aat | p.D5800N |
| COADREAD | 2 | 152376262 | 152376262 | + | Silent | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152376262G>A | c.17397C>T | c.(17395-17397)ttC>ttT | p.F5799F |
| COADREAD | 2 | 152376267 | 152376267 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152376267T>G | c.17392A>C | c.(17392-17394)Aat>Cat | p.N5798H |
| COADREAD | 2 | 152380919 | 152380919 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152380919C>A | c.17282G>T | c.(17281-17283)aGa>aTa | p.R5761I |
| COADREAD | 2 | 152381065 | 152381065 | + | Silent | SNP | G | G | T | TCGA-CK-4948-01B-11D-1650-10 | TCGA-CK-4948-10A-01D-1650-10 | g.chr2:152381065G>T | c.17235C>A | c.(17233-17235)atC>atA | p.I5745I |
| COADREAD | 2 | 152381066 | 152381066 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5860-01A-01D-1650-10 | TCGA-CM-5860-10A-01D-1650-10 | g.chr2:152381066A>G | c.17234T>C | c.(17233-17235)aTc>aCc | p.I5745T |
| COADREAD | 2 | 152381115 | 152381115 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152381115C>A | c.17185G>T | c.(17185-17187)Gat>Tat | p.D5729Y |
| COADREAD | 2 | 152381129 | 152381129 | + | Splice_Site | SNP | A | A | G | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152381129A>G | c.17171T>C | c.(17170-17172)gTc>gCc | p.V5724A |
| COADREAD | 2 | 152381773 | 152381773 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152381773C>A | c.17073G>T | c.(17071-17073)aaG>aaT | p.K5691N |
| COADREAD | 2 | 152382515 | 152382515 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr2:152382515C>A | c.17015G>T | c.(17014-17016)cGg>cTg | p.R5672L |
| COADREAD | 2 | 152382515 | 152382515 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr2:152382515C>A | c.17015G>T | c.(17014-17016)cGg>cTg | p.R5672L |
| COADREAD | 2 | 152382515 | 152382515 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6600-01A-11D-1771-10 | TCGA-AZ-6600-11A-01D-1771-10 | g.chr2:152382515C>A | c.17015G>T | c.(17014-17016)cGg>cTg | p.R5672L |
| COADREAD | 2 | 152382515 | 152382515 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr2:152382515C>T | c.17015G>A | c.(17014-17016)cGg>cAg | p.R5672Q |
| COADREAD | 2 | 152382516 | 152382516 | + | Missense_Mutation | SNP | G | G | A | TCGA-DM-A28F-01A-11D-A16V-10 | TCGA-DM-A28F-10A-01D-A16V-10 | g.chr2:152382516G>A | c.17014C>T | c.(17014-17016)Cgg>Tgg | p.R5672W |
| COADREAD | 2 | 152382516 | 152382516 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6321-01A-11D-1719-10 | TCGA-G4-6321-10A-01D-1720-10 | g.chr2:152382516G>A | c.17014C>T | c.(17014-17016)Cgg>Tgg | p.R5672W |
| COADREAD | 2 | 152382718 | 152382718 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6654-01A-21D-1835-10 | TCGA-A6-6654-10A-01D-1835-10 | g.chr2:152382718G>A | c.16901C>T | c.(16900-16902)aCg>aTg | p.T5634M |
| COADREAD | 2 | 152383462 | 152383462 | + | Silent | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr2:152383462G>A | c.16812C>T | c.(16810-16812)ctC>ctT | p.L5604L |
| COADREAD | 2 | 152390002 | 152390002 | + | Intron | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr2:152390002C>T | | | |
| COADREAD | 2 | 152390743 | 152390743 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152390743C>T | c.16300G>A | c.(16300-16302)Gac>Aac | p.D5434N |
| COADREAD | 2 | 152390743 | 152390743 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152390743C>T | c.16300G>A | c.(16300-16302)Gac>Aac | p.D5434N |
| COADREAD | 2 | 152390749 | 152390749 | + | Missense_Mutation | SNP | C | C | T | TCGA-DC-6158-01A-11D-1657-10 | TCGA-DC-6158-10A-01D-1657-10 | g.chr2:152390749C>T | c.16294G>A | c.(16294-16296)Gca>Aca | p.A5432T |
| COADREAD | 2 | 152393677 | 152393677 | + | Missense_Mutation | SNP | A | A | T | TCGA-DM-A1DA-01A-11D-A152-10 | TCGA-DM-A1DA-10A-01D-A152-10 | g.chr2:152393677A>T | c.16073T>A | c.(16072-16074)cTg>cAg | p.L5358Q |
| COADREAD | 2 | 152393704 | 152393704 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-6751-01A-11D-1835-10 | TCGA-CK-6751-10A-01D-1835-10 | g.chr2:152393704T>C | c.16046A>G | c.(16045-16047)tAt>tGt | p.Y5349C |
| COADREAD | 2 | 152393738 | 152393738 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr2:152393738C>A | c.16012G>T | c.(16012-16014)Gaa>Taa | p.E5338* |
| COADREAD | 2 | 152394412 | 152394412 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr2:152394412G>A | c.15973C>T | c.(15973-15975)Cga>Tga | p.R5325* |
| COADREAD | 2 | 152394477 | 152394477 | + | Missense_Mutation | SNP | T | T | A | TCGA-CK-6747-01A-11D-1835-10 | TCGA-CK-6747-10A-01D-1835-10 | g.chr2:152394477T>A | c.15908A>T | c.(15907-15909)gAg>gTg | p.E5303V |
| COADREAD | 2 | 152396866 | 152396866 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr2:152396866C>T | c.15781G>A | c.(15781-15783)Gcc>Acc | p.A5261T |
| COADREAD | 2 | 152397299 | 152397299 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr2:152397299A>G | c.15596T>C | c.(15595-15597)cTt>cCt | p.L5199P |
| COADREAD | 2 | 152402489 | 152402489 | + | Silent | SNP | C | C | T | TCGA-DC-6682-01A-11D-1826-10 | TCGA-DC-6682-10A-01D-1826-10 | g.chr2:152402489C>T | c.15387G>A | c.(15385-15387)aaG>aaA | p.K5129K |
| COADREAD | 2 | 152402491 | 152402491 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr2:152402491T>C | c.15385A>G | c.(15385-15387)Aag>Gag | p.K5129E |
| COADREAD | 2 | 152402870 | 152402870 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3655-01A-02D-1719-10 | TCGA-AA-3655-11A-01D-1719-10 | g.chr2:152402870G>A | c.15352C>T | c.(15352-15354)Cgg>Tgg | p.R5118W |
| COADREAD | 2 | 152402956 | 152402956 | + | Splice_Site | SNP | A | A | G | TCGA-D5-6529-01A-11D-1771-10 | TCGA-D5-6529-10A-01D-1771-10 | g.chr2:152402956A>G | c.15266T>C | c.(15265-15267)aTt>aCt | p.I5089T |
| COADREAD | 2 | 152406166 | 152406166 | + | Missense_Mutation | SNP | C | C | T | TCGA-AF-6672-01A-11D-1826-10 | TCGA-AF-6672-10A-01D-1826-10 | g.chr2:152406166C>T | c.14930G>A | c.(14929-14931)cGt>cAt | p.R4977H |
| COADREAD | 2 | 152408253 | 152408253 | + | Splice_Site | SNP | G | G | A | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr2:152408253G>A | c.14840C>T | c.(14839-14841)tCg>tTg | p.S4947L |
| COADREAD | 2 | 152408313 | 152408313 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr2:152408313G>A | c.14780C>T | c.(14779-14781)gCt>gTt | p.A4927V |
| COADREAD | 2 | 152409185 | 152409185 | + | Splice_Site | SNP | C | C | T | TCGA-CK-5912-01A-11D-1650-10 | TCGA-CK-5912-10A-01D-1650-10 | g.chr2:152409185C>T | | c.e100+1 | |
| COADREAD | 2 | 152409234 | 152409234 | + | Silent | SNP | A | A | G | TCGA-CM-6168-01A-11D-1650-10 | TCGA-CM-6168-10A-01D-1650-10 | g.chr2:152409234A>G | c.14685T>C | c.(14683-14685)gaT>gaC | p.D4895D |
| COADREAD | 2 | 152410410 | 152410410 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr2:152410410C>T | c.14455G>A | c.(14455-14457)Gaa>Aaa | p.E4819K |
| COADREAD | 2 | 152410418 | 152410418 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr2:152410418C>T | c.14447G>A | c.(14446-14448)cGc>cAc | p.R4816H |
| COADREAD | 2 | 152411488 | 152411488 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr2:152411488G>A | c.14282C>T | c.(14281-14283)cCg>cTg | p.P4761L |
| COADREAD | 2 | 152417136 | 152417136 | + | Silent | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr2:152417136G>A | c.14181C>T | c.(14179-14181)caC>caT | p.H4727H |
| COADREAD | 2 | 152417606 | 152417606 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152417606T>C | c.14015A>G | c.(14014-14016)aAt>aGt | p.N4672S |
| COADREAD | 2 | 152417610 | 152417610 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152417610C>A | c.14011G>T | c.(14011-14013)Gaa>Taa | p.E4671* |
| COADREAD | 2 | 152419150 | 152419150 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152419150C>T | c.13763G>A | c.(13762-13764)cGa>cAa | p.R4588Q |
| COADREAD | 2 | 152421647 | 152421647 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3848-01A-01W-0900-09 | TCGA-AA-3848-10A-01W-0900-09 | g.chr2:152421647T>A | c.13279A>T | c.(13279-13281)Aca>Tca | p.T4427S |
| COADREAD | 2 | 152421648 | 152421648 | + | Missense_Mutation | SNP | T | T | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152421648T>G | c.13278A>C | c.(13276-13278)gaA>gaC | p.E4426D |
| COADREAD | 2 | 152423723 | 152423723 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr2:152423723C>T | c.13012G>A | c.(13012-13014)Gat>Aat | p.D4338N |
| COADREAD | 2 | 152423966 | 152423966 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152423966G>A | c.12769C>T | c.(12769-12771)Caa>Taa | p.Q4257* |
| COADREAD | 2 | 152425130 | 152425130 | + | Splice_Site | SNP | A | A | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152425130A>G | | c.e83+1 | |
| COADREAD | 2 | 152426656 | 152426656 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152426656G>A | c.12266C>T | c.(12265-12267)aCc>aTc | p.T4089I |
| COADREAD | 2 | 152432753 | 152432753 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3848-01A-01W-0900-09 | TCGA-AA-3848-10A-01W-0900-09 | g.chr2:152432753C>T | c.11717G>A | c.(11716-11718)cGg>cAg | p.R3906Q |
| COADREAD | 2 | 152432808 | 152432808 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-3810-01A-01W-0995-10 | TCGA-A6-3810-11A-01W-0995-10 | g.chr2:152432808G>A | c.11662C>T | c.(11662-11664)Cct>Tct | p.P3888S |
| COADREAD | 2 | 152466495 | 152466495 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6607-01A-11D-1835-10 | TCGA-AZ-6607-11A-01D-1835-10 | g.chr2:152466495T>C | c.11429A>G | c.(11428-11430)aAg>aGg | p.K3810R |
| COADREAD | 2 | 152466553 | 152466553 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152466553A>G | c.11371T>C | c.(11371-11373)Tgt>Cgt | p.C3791R |
| COADREAD | 2 | 152467090 | 152467090 | + | Silent | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152467090A>G | c.11229T>C | c.(11227-11229)gaT>gaC | p.D3743D |
| COADREAD | 2 | 152468788 | 152468788 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152468788C>T | c.10988G>A | c.(10987-10989)cGc>cAc | p.R3663H |
| COADREAD | 2 | 152468789 | 152468789 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152468789G>A | c.10987C>T | c.(10987-10989)Cgc>Tgc | p.R3663C |
| COADREAD | 2 | 152470797 | 152470797 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6600-01A-11D-1771-10 | TCGA-AZ-6600-11A-01D-1771-10 | g.chr2:152470797T>C | c.10865A>G | c.(10864-10866)cAg>cGg | p.Q3622R |
| COADREAD | 2 | 152471030 | 152471030 | + | Silent | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152471030C>T | c.10632G>A | c.(10630-10632)ccG>ccA | p.P3544P |
| COADREAD | 2 | 152471049 | 152471049 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr2:152471049C>A | c.10613G>T | c.(10612-10614)cGg>cTg | p.R3538L |
| COADREAD | 2 | 152471049 | 152471049 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr2:152471049C>T | c.10613G>A | c.(10612-10614)cGg>cAg | p.R3538Q |
| COADREAD | 2 | 152471050 | 152471050 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr2:152471050G>A | c.10612C>T | c.(10612-10614)Cgg>Tgg | p.R3538W |
| COADREAD | 2 | 152471050 | 152471050 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-5348-01A-21D-1719-10 | TCGA-CM-5348-10A-01D-1719-10 | g.chr2:152471050G>A | c.10612C>T | c.(10612-10614)Cgg>Tgg | p.R3538W |
| COADREAD | 2 | 152472613 | 152472613 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152472613T>G | c.10463A>C | c.(10462-10464)aAa>aCa | p.K3488T |
| COADREAD | 2 | 152476060 | 152476060 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152476060C>T | c.10048G>A | c.(10048-10050)Gat>Aat | p.D3350N |
| COADREAD | 2 | 152477450 | 152477450 | + | Silent | SNP | G | G | T | TCGA-G4-6299-01A-11D-1771-10 | TCGA-G4-6299-10A-01D-1771-10 | g.chr2:152477450G>T | c.9814C>A | c.(9814-9816)Cgg>Agg | p.R3272R |
| COADREAD | 2 | 152482051 | 152482051 | + | Silent | SNP | A | A | G | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr2:152482051A>G | c.9720T>C | c.(9718-9720)agT>agC | p.S3240S |
| COADREAD | 2 | 152482051 | 152482051 | + | Silent | SNP | A | A | G | TCGA-CM-6168-01A-11D-1650-10 | TCGA-CM-6168-10A-01D-1650-10 | g.chr2:152482051A>G | c.9720T>C | c.(9718-9720)agT>agC | p.S3240S |
| COADREAD | 2 | 152482077 | 152482077 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr2:152482077C>T | c.9694G>A | c.(9694-9696)Gca>Aca | p.A3232T |
| COADREAD | 2 | 152483635 | 152483635 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr2:152483635C>A | c.9499G>T | c.(9499-9501)Gct>Tct | p.A3167S |
| COADREAD | 2 | 152484190 | 152484190 | + | Silent | SNP | G | G | A | TCGA-AA-3818-01A-01W-0900-09 | TCGA-AA-3818-10A-01W-0900-09 | g.chr2:152484190G>A | c.9261C>T | c.(9259-9261)agC>agT | p.S3087S |
| COADREAD | 2 | 152484275 | 152484275 | + | Missense_Mutation | SNP | T | T | C | TCGA-DY-A1DF-01A-11D-A152-10 | TCGA-DY-A1DF-10A-01D-A152-10 | g.chr2:152484275T>C | c.9176A>G | c.(9175-9177)aAg>aGg | p.K3059R |
| COADREAD | 2 | 152496964 | 152496964 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152496964C>T | c.8590G>A | c.(8590-8592)Gat>Aat | p.D2864N |
| COADREAD | 2 | 152497158 | 152497158 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152497158C>T | c.8396G>A | c.(8395-8397)cGt>cAt | p.R2799H |
| COADREAD | 2 | 152500443 | 152500443 | + | Silent | SNP | G | G | A | TCGA-AG-4005-01A-01W-1073-09 | TCGA-AG-4005-10A-01W-1073-09 | g.chr2:152500443G>A | c.7845C>T | c.(7843-7845)tgC>tgT | p.C2615C |
| COADREAD | 2 | 152500575 | 152500575 | + | Silent | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr2:152500575G>A | c.7713C>T | c.(7711-7713)gaC>gaT | p.D2571D |
| COADREAD | 2 | 152501066 | 152501066 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152501066C>A | c.7560G>T | c.(7558-7560)gaG>gaT | p.E2520D |
| COADREAD | 2 | 152502711 | 152502711 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr2:152502711T>C | c.7469A>G | c.(7468-7470)cAg>cGg | p.Q2490R |
| COADREAD | 2 | 152502747 | 152502747 | + | Splice_Site | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152502747C>T | c.7433G>A | c.(7432-7434)aGa>aAa | p.R2478K |
| COADREAD | 2 | 152506778 | 152506778 | + | Missense_Mutation | SNP | C | C | T | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr2:152506778C>T | c.7343G>A | c.(7342-7344)cGt>cAt | p.R2448H |
| COADREAD | 2 | 152506779 | 152506779 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152506779G>A | c.7342C>T | c.(7342-7344)Cgt>Tgt | p.R2448C |
| COADREAD | 2 | 152506779 | 152506779 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152506779G>A | c.7342C>T | c.(7342-7344)Cgt>Tgt | p.R2448C |
| COADREAD | 2 | 152506794 | 152506794 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A01W-01A-21W-A096-10 | TCGA-AG-A01W-11A-11W-A096-10 | g.chr2:152506794T>G | c.7327A>C | c.(7327-7329)Agt>Cgt | p.S2443R |
| COADREAD | 2 | 152506854 | 152506854 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152506854C>A | c.7267G>T | c.(7267-7269)Gga>Tga | p.G2423* |
| COADREAD | 2 | 152507181 | 152507181 | + | Silent | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr2:152507181G>A | c.7134C>T | c.(7132-7134)gaC>gaT | p.D2378D |
| COADREAD | 2 | 152507262 | 152507262 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152507262C>A | c.7053G>T | c.(7051-7053)gaG>gaT | p.E2351D |
| COADREAD | 2 | 152511795 | 152511795 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152511795G>A | c.6796C>T | c.(6796-6798)Ctg>Ttg | p.L2266L |
| COADREAD | 2 | 152512413 | 152512413 | + | Missense_Mutation | SNP | T | T | C | TCGA-DY-A1DG-01A-11D-A152-10 | TCGA-DY-A1DG-10A-01D-A152-10 | g.chr2:152512413T>C | c.6620A>G | c.(6619-6621)cAc>cGc | p.H2207R |
| COADREAD | 2 | 152512665 | 152512665 | + | Splice_Site | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152512665A>G | | c.e49+1 | |
| COADREAD | 2 | 152512773 | 152512773 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr2:152512773G>A | c.6389C>T | c.(6388-6390)gCc>gTc | p.A2130V |
| COADREAD | 2 | 152512926 | 152512926 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152512926C>T | c.6236G>A | c.(6235-6237)cGc>cAc | p.R2079H |
| COADREAD | 2 | 152514562 | 152514562 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr2:152514562A>G | c.6118T>C | c.(6118-6120)Tat>Cat | p.Y2040H |
| COADREAD | 2 | 152515676 | 152515676 | + | Missense_Mutation | SNP | T | T | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr2:152515676T>A | c.5978A>T | c.(5977-5979)tAc>tTc | p.Y1993F |
| COADREAD | 2 | 152518760 | 152518760 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152518760C>A | c.5859G>T | c.(5857-5859)gaG>gaT | p.E1953D |
| COADREAD | 2 | 152518781 | 152518781 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152518781C>A | c.5838G>T | c.(5836-5838)gaG>gaT | p.E1946D |
| COADREAD | 2 | 152520264 | 152520264 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr2:152520264G>A | c.5561C>T | c.(5560-5562)tCa>tTa | p.S1854L |
| COADREAD | 2 | 152521901 | 152521901 | + | Silent | SNP | G | G | A | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr2:152521901G>A | c.5184C>T | c.(5182-5184)gcC>gcT | p.A1728A |
| COADREAD | 2 | 152521949 | 152521949 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152521949A>C | c.5136T>G | c.(5134-5136)agT>agG | p.S1712R |
| COADREAD | 2 | 152521993 | 152521993 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr2:152521993A>G | c.5092T>C | c.(5092-5094)Tcc>Ccc | p.S1698P |
| COADREAD | 2 | 152522794 | 152522794 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr2:152522794T>C | c.4841A>G | c.(4840-4842)tAc>tGc | p.Y1614C |
| COADREAD | 2 | 152522864 | 152522864 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152522864G>T | c.4771C>A | c.(4771-4773)Ctc>Atc | p.L1591I |
| COADREAD | 2 | 152522864 | 152522864 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152522864G>T | c.4771C>A | c.(4771-4773)Ctc>Atc | p.L1591I |
| COADREAD | 2 | 152522908 | 152522908 | + | Missense_Mutation | SNP | T | T | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr2:152522908T>C | c.4727A>G | c.(4726-4728)tAt>tGt | p.Y1576C |
| COADREAD | 2 | 152527556 | 152527556 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:152527556T>C | c.4487A>G | c.(4486-4488)aAc>aGc | p.N1496S |
| COADREAD | 2 | 152527651 | 152527651 | + | Silent | SNP | G | G | A | TCGA-AA-3837-01A-01W-0900-09 | TCGA-AA-3837-10A-01W-0900-09 | g.chr2:152527651G>A | c.4392C>T | c.(4390-4392)ggC>ggT | p.G1464G |
| COADREAD | 2 | 152527669 | 152527669 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152527669C>A | c.4374G>T | c.(4372-4374)gaG>gaT | p.E1458D |
| COADREAD | 2 | 152528901 | 152528901 | + | Silent | SNP | G | G | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr2:152528901G>T | c.4281C>A | c.(4279-4281)gtC>gtA | p.V1427V |
| COADREAD | 2 | 152528930 | 152528930 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr2:152528930C>T | c.4252G>A | c.(4252-4254)Gcc>Acc | p.A1418T |
| COADREAD | 2 | 152528931 | 152528931 | + | Silent | SNP | G | G | A | TCGA-D5-6534-01A-21D-1924-10 | TCGA-D5-6534-10A-01D-1924-10 | g.chr2:152528931G>A | c.4251C>T | c.(4249-4251)gaC>gaT | p.D1417D |
| COADREAD | 2 | 152529066 | 152529066 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152529066C>A | c.4116G>T | c.(4114-4116)aaG>aaT | p.K1372N |
| COADREAD | 2 | 152529149 | 152529149 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:152529149C>T | c.4033G>A | c.(4033-4035)Ggt>Agt | p.G1345S |
| COADREAD | 2 | 152534213 | 152534213 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152534213C>T | c.3640G>A | c.(3640-3642)Gaa>Aaa | p.E1214K |
| COADREAD | 2 | 152534213 | 152534213 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr2:152534213C>T | c.3640G>A | c.(3640-3642)Gaa>Aaa | p.E1214K |
| COADREAD | 2 | 152534219 | 152534219 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152534219C>T | c.3634G>A | c.(3634-3636)Gac>Aac | p.D1212N |
| COADREAD | 2 | 152534541 | 152534541 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6606-01A-11D-1835-10 | TCGA-AZ-6606-11A-01D-1835-10 | g.chr2:152534541G>A | c.3416C>T | c.(3415-3417)aCg>aTg | p.T1139M |
| COADREAD | 2 | 152534587 | 152534587 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152534587G>A | c.3370C>T | c.(3370-3372)Cgg>Tgg | p.R1124W |
| COADREAD | 2 | 152536255 | 152536255 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr2:152536255C>A | c.3235G>T | c.(3235-3237)Gcc>Tcc | p.A1079S |
| COADREAD | 2 | 152536488 | 152536488 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr2:152536488G>A | c.3091C>T | c.(3091-3093)Cca>Tca | p.P1031S |
| COADREAD | 2 | 152541326 | 152541326 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152541326T>C | c.2801A>G | c.(2800-2802)gAc>gGc | p.D934G |
| COADREAD | 2 | 152541391 | 152541391 | + | Silent | SNP | G | G | A | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr2:152541391G>A | c.2736C>T | c.(2734-2736)gcC>gcT | p.A912A |
| COADREAD | 2 | 152541479 | 152541479 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152541479C>T | c.2648G>A | c.(2647-2649)cGa>cAa | p.R883Q |
| COADREAD | 2 | 152543972 | 152543972 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr2:152543972C>A | c.2598G>T | c.(2596-2598)aaG>aaT | p.K866N |
| COADREAD | 2 | 152544143 | 152544143 | + | Silent | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr2:152544143G>A | c.2520C>T | c.(2518-2520)agC>agT | p.S840S |
| COADREAD | 2 | 152544209 | 152544209 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152544209C>A | c.2454G>T | c.(2452-2454)aaG>aaT | p.K818N |
| COADREAD | 2 | 152544228 | 152544228 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr2:152544228C>A | c.2435G>T | c.(2434-2436)tGg>tTg | p.W812L |
| COADREAD | 2 | 152548407 | 152548407 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152548407C>A | c.2182G>T | c.(2182-2184)Gca>Tca | p.A728S |
| COADREAD | 2 | 152548416 | 152548416 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152548416C>T | c.2173G>A | c.(2173-2175)Gaa>Aaa | p.E725K |
| COADREAD | 2 | 152548637 | 152548637 | + | Missense_Mutation | SNP | T | T | A | TCGA-DM-A1D7-01A-11D-A152-10 | TCGA-DM-A1D7-10A-01D-A152-10 | g.chr2:152548637T>A | c.2042A>T | c.(2041-2043)tAt>tTt | p.Y681F |
| COADREAD | 2 | 152548665 | 152548665 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:152548665A>C | c.2014T>G | c.(2014-2016)Tta>Gta | p.L672V |
| COADREAD | 2 | 152548665 | 152548665 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152548665A>C | c.2014T>G | c.(2014-2016)Tta>Gta | p.L672V |
| COADREAD | 2 | 152548870 | 152548870 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152548870A>G | c.1903T>C | c.(1903-1905)Tac>Cac | p.Y635H |
| COADREAD | 2 | 152550884 | 152550884 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr2:152550884C>T | c.1849G>A | c.(1849-1851)Gat>Aat | p.D617N |
| COADREAD | 2 | 152550885 | 152550885 | + | Silent | SNP | G | G | A | TCGA-A6-5657-01A-01D-1650-10 | TCGA-A6-5657-10A-01D-1650-10 | g.chr2:152550885G>A | c.1848C>T | c.(1846-1848)gaC>gaT | p.D616D |
| COADREAD | 2 | 152550899 | 152550899 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr2:152550899G>A | c.1834C>T | c.(1834-1836)Ctc>Ttc | p.L612F |
| COADREAD | 2 | 152550922 | 152550922 | + | Missense_Mutation | SNP | T | T | G | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:152550922T>G | c.1811A>C | c.(1810-1812)aAc>aCc | p.N604T |
| COADREAD | 2 | 152550935 | 152550935 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152550935C>A | c.1798G>T | c.(1798-1800)Gac>Tac | p.D600Y |
| COADREAD | 2 | 152552108 | 152552108 | + | Missense_Mutation | SNP | G | G | A | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr2:152552108G>A | c.1658C>T | c.(1657-1659)gCc>gTc | p.A553V |
| COADREAD | 2 | 152552144 | 152552144 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr2:152552144delG | c.1622delC | c.(1621-1623)cctfs | p.P541fs |
| COADREAD | 2 | 152552161 | 152552161 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr2:152552161G>T | c.1605C>A | c.(1603-1605)ttC>ttA | p.F535L |
| COADREAD | 2 | 152554088 | 152554088 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152554088G>A | c.1227C>T | c.(1225-1227)ctC>ctT | p.L409L |
| COADREAD | 2 | 152563485 | 152563485 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:152563485C>A | c.1062G>T | c.(1060-1062)aaG>aaT | p.K354N |
| COADREAD | 2 | 152566209 | 152566209 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152566209C>A | c.996G>T | c.(994-996)gaG>gaT | p.E332D |
| COADREAD | 2 | 152579948 | 152579948 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:152579948T>G | c.665A>C | c.(664-666)aAt>aCt | p.N222T |
| COADREAD | 2 | 152580800 | 152580800 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr2:152580800C>T | c.586G>A | c.(586-588)Gtt>Att | p.V196I |
| COADREAD | 2 | 152582036 | 152582036 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr2:152582036C>A | c.333G>T | c.(331-333)caG>caT | p.Q111H |
| COADREAD | 2 | 152582046 | 152582046 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr2:152582046G>A | c.323C>T | c.(322-324)aCa>aTa | p.T108I |
| COADREAD | 2 | 152582047 | 152582047 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3712-01A-21D-1719-10 | TCGA-AA-3712-11A-01D-1719-10 | g.chr2:152582047T>C | c.322A>G | c.(322-324)Aca>Gca | p.T108A |
| COADREAD | 2 | 152582047 | 152582047 | + | Missense_Mutation | SNP | T | T | C | TCGA-DT-5265-01A-21D-1826-10 | TCGA-DT-5265-10A-01D-1826-10 | g.chr2:152582047T>C | c.322A>G | c.(322-324)Aca>Gca | p.T108A |
| COADREAD | 2 | 152584337 | 152584337 | + | Silent | SNP | C | C | T | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr2:152584337C>T | c.162G>A | c.(160-162)caG>caA | p.Q54Q |
| COADREAD | 2 | 152589659 | 152589659 | + | Silent | SNP | G | G | A | TCGA-G4-6303-01A-11D-1771-10 | TCGA-G4-6303-10A-01D-1771-10 | g.chr2:152589659G>A | c.12C>T | c.(10-12)gaC>gaT | p.D4D |
| DLBC | 2 | 152382759 | 152382759 | + | Silent | SNP | T | T | C | TCGA-G8-6909-01A-11D-2210-10 | TCGA-G8-6909-14A-01D-2210-10 | g.chr2:152382759T>C | c.16860A>G | c.(16858-16860)aaA>aaG | p.K5620K |
| DLBC | 2 | 152389991 | 152389991 | + | Intron | SNP | A | A | G | TCGA-G8-6909-01A-11D-2210-10 | TCGA-G8-6909-14A-01D-2210-10 | g.chr2:152389991A>G | | | |
| DLBC | 2 | 152420390 | 152420390 | + | Missense_Mutation | SNP | C | C | T | TCGA-RQ-A68N-01A-11D-A31X-10 | TCGA-RQ-A68N-10A-01D-A31X-10 | g.chr2:152420390C>T | c.13423G>A | c.(13423-13425)Gag>Aag | p.E4475K |
| DLBC | 2 | 152432215 | 152432215 | + | Silent | SNP | C | C | A | TCGA-FF-8046-01A-11D-2210-10 | TCGA-FF-8046-10A-01D-2210-10 | g.chr2:152432215C>A | c.11904G>T | c.(11902-11904)gtG>gtT | p.V3968V |
| DLBC | 2 | 152432838 | 152432838 | + | Missense_Mutation | SNP | G | G | A | TCGA-FA-A7DS-01A-11D-A382-10 | TCGA-FA-A7DS-10A-01D-A385-10 | g.chr2:152432838G>A | c.11632C>T | c.(11632-11634)Cgt>Tgt | p.R3878C |
| DLBC | 2 | 152470904 | 152470904 | + | Silent | SNP | C | C | T | TCGA-FF-8061-01A-11D-2210-10 | TCGA-FF-8061-10A-01D-2210-10 | g.chr2:152470904C>T | c.10758G>A | c.(10756-10758)aaG>aaA | p.K3586K |
| DLBC | 2 | 152486080 | 152486080 | + | Silent | SNP | G | G | T | TCGA-FA-A6HN-01A-11D-A31X-10 | TCGA-FA-A6HN-10A-01D-A31X-10 | g.chr2:152486080G>T | c.9075C>A | c.(9073-9075)gcC>gcA | p.A3025A |
| DLBC | 2 | 152486101 | 152486101 | + | Silent | SNP | G | G | A | TCGA-FA-A7Q1-01A-11D-A382-10 | TCGA-FA-A7Q1-10A-01D-A385-10 | g.chr2:152486101G>A | c.9054C>T | c.(9052-9054)gaC>gaT | p.D3018D |
| DLBC | 2 | 152536281 | 152536281 | + | Missense_Mutation | SNP | G | G | A | TCGA-FF-8047-01A-11D-2210-10 | TCGA-FF-8047-10A-01D-2210-10 | g.chr2:152536281G>A | c.3209C>T | c.(3208-3210)gCg>gTg | p.A1070V |
| DLBC | 2 | 152547268 | 152547268 | + | Silent | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr2:152547268G>A | c.2283C>T | c.(2281-2283)gcC>gcT | p.A761A |
| ESCA | 2 | 152348691 | 152348691 | + | Missense_Mutation | SNP | G | G | T | TCGA-LN-A7HX-01A-11D-A33E-09 | TCGA-LN-A7HX-10A-01D-A33H-09 | g.chr2:152348691G>T | c.19410C>A | c.(19408-19410)gaC>gaA | p.D6470E |
| ESCA | 2 | 152348986 | 152348986 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A4OF-01A-11D-A27G-09 | TCGA-L5-A4OF-11A-12D-A27G-09 | g.chr2:152348986C>T | c.19220G>A | c.(19219-19221)cGg>cAg | p.R6407Q |
| ESCA | 2 | 152350344 | 152350344 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr2:152350344G>T | c.19049C>A | c.(19048-19050)aCa>aAa | p.T6350K |
| ESCA | 2 | 152362681 | 152362681 | + | Splice_Site | SNP | G | G | A | TCGA-2H-A9GI-01A-11D-A37C-09 | TCGA-2H-A9GI-11A-11D-A37F-09 | g.chr2:152362681G>A | c.18545C>T | c.(18544-18546)tCg>tTg | p.S6182L |
| ESCA | 2 | 152392295 | 152392295 | + | Missense_Mutation | SNP | T | T | G | TCGA-R6-A6KZ-01A-11D-A31U-09 | TCGA-R6-A6KZ-10A-01D-A31U-09 | g.chr2:152392295T>G | c.16119A>C | c.(16117-16119)gaA>gaC | p.E5373D |
| ESCA | 2 | 152402931 | 152402931 | + | Silent | SNP | G | G | T | TCGA-L5-A4OQ-01A-11D-A27G-09 | TCGA-L5-A4OQ-11A-12D-A27G-09 | g.chr2:152402931G>T | c.15291C>A | c.(15289-15291)gtC>gtA | p.V5097V |
| ESCA | 2 | 152409288 | 152409288 | + | Silent | SNP | G | G | T | TCGA-L5-A4OE-01A-11D-A27G-09 | TCGA-L5-A4OE-11A-11D-A27G-09 | g.chr2:152409288G>T | c.14631C>A | c.(14629-14631)atC>atA | p.I4877I |
| ESCA | 2 | 152410372 | 152410372 | + | Silent | SNP | G | G | A | TCGA-L5-A43J-01A-12D-A247-09 | TCGA-L5-A43J-11A-11D-A247-09 | g.chr2:152410372G>A | c.14493C>T | c.(14491-14493)caC>caT | p.H4831H |
| ESCA | 2 | 152411479 | 152411479 | + | Missense_Mutation | SNP | G | G | A | TCGA-LN-A49U-01A-31D-A27G-09 | TCGA-LN-A49U-10A-01D-A27G-09 | g.chr2:152411479G>A | c.14291C>T | c.(14290-14292)gCa>gTa | p.A4764V |
| ESCA | 2 | 152420128 | 152420128 | + | Silent | SNP | T | T | G | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr2:152420128T>G | c.13582A>C | c.(13582-13584)Agg>Cgg | p.R4528R |
| ESCA | 2 | 152424871 | 152424871 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr2:152424871delG | c.12592delC | c.(12592-12594)ctgfs | p.L4199fs |
| ESCA | 2 | 152425154 | 152425154 | + | Missense_Mutation | SNP | T | T | C | TCGA-LN-A4A5-01A-21D-A27G-09 | TCGA-LN-A4A5-10A-01D-A27G-09 | g.chr2:152425154T>C | c.12509A>G | c.(12508-12510)cAa>cGa | p.Q4170R |
| ESCA | 2 | 152432749 | 152432749 | + | Silent | SNP | C | C | T | TCGA-Z6-A9VB-01A-21D-A37C-09 | TCGA-Z6-A9VB-10A-01D-A37F-09 | g.chr2:152432749C>T | c.11721G>A | c.(11719-11721)acG>acA | p.T3907T |
| ESCA | 2 | 152435902 | 152435902 | + | Intron | SNP | C | C | T | TCGA-LN-A7HZ-01A-31D-A351-09 | TCGA-LN-A7HZ-10A-01D-A351-09 | g.chr2:152435902C>T | | | |
| ESCA | 2 | 152436107 | 152436107 | + | Intron | SNP | G | G | A | TCGA-L5-A88W-01A-11D-A351-09 | TCGA-L5-A88W-11A-11D-A351-09 | g.chr2:152436107G>A | | | |
| ESCA | 2 | 152448643 | 152448643 | + | Intron | SNP | G | G | A | TCGA-IG-A8O2-01A-11D-A36J-09 | TCGA-IG-A8O2-10A-01D-A36M-09 | g.chr2:152448643G>A | | | |
| ESCA | 2 | 152450810 | 152450810 | + | Intron | SNP | C | C | T | TCGA-ZR-A9CJ-01B-11D-A387-09 | TCGA-ZR-A9CJ-10A-01D-A38A-09 | g.chr2:152450810C>T | | | |
| ESCA | 2 | 152466583 | 152466583 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-L5-A88V-01A-11D-A351-09 | TCGA-L5-A88V-11A-11D-A351-09 | g.chr2:152466583G>A | c.11341C>T | c.(11341-11343)Cag>Tag | p.Q3781* |
| ESCA | 2 | 152468716 | 152468716 | + | Missense_Mutation | SNP | G | G | A | TCGA-IG-A97H-01A-11D-A387-09 | TCGA-IG-A97H-10A-01D-A38A-09 | g.chr2:152468716G>A | c.11060C>T | c.(11059-11061)gCc>gTc | p.A3687V |
| ESCA | 2 | 152471049 | 152471049 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A4A3-01A-11D-A27G-09 | TCGA-LN-A4A3-10A-01D-A27G-09 | g.chr2:152471049C>T | c.10613G>A | c.(10612-10614)cGg>cAg | p.R3538Q |
| ESCA | 2 | 152471079 | 152471079 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A8NI-01A-11D-A37C-09 | TCGA-L5-A8NI-11A-11D-A37F-09 | g.chr2:152471079C>T | c.10583G>A | c.(10582-10584)cGc>cAc | p.R3528H |
| ESCA | 2 | 152492780 | 152492780 | + | Intron | SNP | G | G | T | TCGA-2H-A9GF-01A-11D-A37C-09 | TCGA-2H-A9GF-11A-11D-A37F-09 | g.chr2:152492780G>T | | | |
| ESCA | 2 | 152512796 | 152512796 | + | Silent | SNP | G | G | T | TCGA-VR-AA7B-01A-31D-A403-09 | TCGA-VR-AA7B-10A-01D-A403-09 | g.chr2:152512796G>T | c.6366C>A | c.(6364-6366)gtC>gtA | p.V2122V |
| ESCA | 2 | 152521956 | 152521956 | + | Missense_Mutation | SNP | A | A | C | TCGA-L5-A8NH-01A-11D-A37C-09 | TCGA-L5-A8NH-11A-11D-A37F-09 | g.chr2:152521956A>C | c.5129T>G | c.(5128-5130)aTt>aGt | p.I1710S |
| ESCA | 2 | 152525591 | 152525591 | + | Missense_Mutation | SNP | C | C | T | TCGA-IG-A3YB-01A-11D-A247-09 | TCGA-IG-A3YB-10A-01D-A247-09 | g.chr2:152525591C>T | c.4561G>A | c.(4561-4563)Gaa>Aaa | p.E1521K |
| ESCA | 2 | 152528931 | 152528931 | + | Silent | SNP | G | G | A | TCGA-V5-A7RB-01A-11D-A351-09 | TCGA-V5-A7RB-10A-01D-A351-09 | g.chr2:152528931G>A | c.4251C>T | c.(4249-4251)gaC>gaT | p.D1417D |
| ESCA | 2 | 152531850 | 152531850 | + | Missense_Mutation | SNP | T | T | C | TCGA-V5-A7RE-01A-11D-A351-09 | TCGA-V5-A7RE-10A-01D-A351-09 | g.chr2:152531850T>C | c.3830A>G | c.(3829-3831)gAt>gGt | p.D1277G |
| ESCA | 2 | 152534587 | 152534587 | + | Silent | SNP | G | G | T | TCGA-L5-A8NN-01A-11D-A37C-09 | TCGA-L5-A8NN-11A-11D-A37F-09 | g.chr2:152534587G>T | c.3370C>A | c.(3370-3372)Cgg>Agg | p.R1124R |
| ESCA | 2 | 152544898 | 152544898 | + | Missense_Mutation | SNP | C | C | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr2:152544898C>A | c.2323G>T | c.(2323-2325)Gca>Tca | p.A775S |
| ESCA | 2 | 152548623 | 152548623 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-XP-A8T7-01A-11D-A36J-09 | TCGA-XP-A8T7-10A-01D-A36M-09 | g.chr2:152548623C>A | c.2056G>T | c.(2056-2058)Gag>Tag | p.E686* |
| ESCA | 2 | 152550851 | 152550851 | + | Missense_Mutation | SNP | T | T | G | TCGA-L5-A4OH-01A-11D-A27G-09 | TCGA-L5-A4OH-11A-11D-A27G-09 | g.chr2:152550851T>G | c.1882A>C | c.(1882-1884)Aaa>Caa | p.K628Q |
| GBM | 2 | 152363440 | 152363440 | + | Missense_Mutation | SNP | G | G | T | TCGA-28-5211-01C-11D-1845-08 | TCGA-28-5211-10B-01D-1845-08 | g.chr2:152363440G>T | c.18436C>A | c.(18436-18438)Cag>Aag | p.Q6146K |
| GBM | 2 | 152425820 | 152425820 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-1823-01A-01W-0643-08 | TCGA-14-1823-10A-01W-0644-08 | g.chr2:152425820C>T | c.12394G>A | c.(12394-12396)Gtc>Atc | p.V4132I |
| GBM | 2 | 152470900 | 152470900 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-19-2623-01A-01D-1495-08 | TCGA-19-2623-10A-01D-1495-08 | g.chr2:152470900G>A | c.10762C>T | c.(10762-10764)Cag>Tag | p.Q3588* |
| GBM | 2 | 152476016 | 152476016 | + | Silent | SNP | G | G | A | TCGA-06-6391-01A-11D-1696-08 | TCGA-06-6391-10A-01D-1696-08 | g.chr2:152476016G>A | c.10092C>T | c.(10090-10092)ccC>ccT | p.P3364P |
| GBM | 2 | 152477436 | 152477436 | + | Silent | SNP | A | A | G | TCGA-12-0616-01A-01D-1492-08 | TCGA-12-0616-10A-01D-1492-08 | g.chr2:152477436A>G | c.9828T>C | c.(9826-9828)agT>agC | p.S3276S |
| GBM | 2 | 152484105 | 152484105 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-1753-01A-01D-1494-08 | TCGA-28-1753-10B-01D-1494-08 | g.chr2:152484105C>T | c.9346G>A | c.(9346-9348)Gag>Aag | p.E3116K |
| GBM | 2 | 152518698 | 152518698 | + | Missense_Mutation | SNP | T | T | C | TCGA-19-2629-01A-01D-1495-08 | TCGA-19-2629-10A-01D-1495-08 | g.chr2:152518698T>C | c.5921A>G | c.(5920-5922)gAc>gGc | p.D1974G |
| GBM | 2 | 152580858 | 152580858 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-41-3392-01A-01D-1495-08 | TCGA-41-3392-10A-01D-1495-08 | g.chr2:152580858C>T | c.528G>A | c.(526-528)tgG>tgA | p.W176* |
| GBMLGG | 2 | 152342397 | 152342397 | + | Silent | SNP | C | C | T | TCGA-DH-5142-01A-01D-1468-08 | TCGA-DH-5142-10A-01D-1468-08 | g.chr2:152342397C>T | c.19887G>A | c.(19885-19887)gtG>gtA | p.V6629V |
| GBMLGG | 2 | 152363440 | 152363440 | + | Missense_Mutation | SNP | G | G | T | TCGA-28-5211-01C-11D-1845-08 | TCGA-28-5211-10B-01D-1845-08 | g.chr2:152363440G>T | c.18436C>A | c.(18436-18438)Cag>Aag | p.Q6146K |
| GBMLGG | 2 | 152374910 | 152374910 | + | Missense_Mutation | SNP | C | C | G | TCGA-E1-5307-01A-01D-1893-08 | TCGA-E1-5307-10A-01D-1893-08 | g.chr2:152374910C>G | c.17619G>C | c.(17617-17619)aaG>aaC | p.K5873N |
| GBMLGG | 2 | 152376199 | 152376199 | + | Missense_Mutation | SNP | C | C | T | TCGA-E1-5307-01A-01D-1893-08 | TCGA-E1-5307-10A-01D-1893-08 | g.chr2:152376199C>T | c.17460G>A | c.(17458-17460)atG>atA | p.M5820I |
| GBMLGG | 2 | 152383461 | 152383461 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-7301-01A-11D-2086-08 | TCGA-DU-7301-10A-01D-2086-08 | g.chr2:152383461C>T | c.16813G>A | c.(16813-16815)Gcc>Acc | p.A5605T |
| GBMLGG | 2 | 152406213 | 152406213 | + | Silent | SNP | A | A | G | TCGA-DB-5273-01A-01D-1468-08 | TCGA-DB-5273-10A-01D-1468-08 | g.chr2:152406213A>G | c.14883T>C | c.(14881-14883)taT>taC | p.Y4961Y |
| GBMLGG | 2 | 152409920 | 152409920 | + | Missense_Mutation | SNP | G | G | A | TCGA-CS-5396-01A-02D-1468-08 | TCGA-CS-5396-10A-01D-1468-08 | g.chr2:152409920G>A | c.14620C>T | c.(14620-14622)Cgt>Tgt | p.R4874C |
| GBMLGG | 2 | 152409936 | 152409936 | + | Silent | SNP | C | C | T | TCGA-P5-A5ET-01A-11D-A27K-08 | TCGA-P5-A5ET-10A-01D-A27N-08 | g.chr2:152409936C>T | c.14604G>A | c.(14602-14604)aaG>aaA | p.K4868K |
| GBMLGG | 2 | 152410491 | 152410491 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152410491C>T | c.14374G>A | c.(14374-14376)Gtg>Atg | p.V4792M |
| GBMLGG | 2 | 152420364 | 152420364 | + | Silent | SNP | G | G | A | TCGA-TQ-A7RN-01A-11D-A33T-08 | TCGA-TQ-A7RN-10A-01D-A33W-08 | g.chr2:152420364G>A | c.13449C>T | c.(13447-13449)gcC>gcT | p.A4483A |
| GBMLGG | 2 | 152422294 | 152422294 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152422294C>T | c.13094G>A | c.(13093-13095)gGc>gAc | p.G4365D |
| GBMLGG | 2 | 152423688 | 152423688 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152423688C>A | c.13047G>T | c.(13045-13047)caG>caT | p.Q4349H |
| GBMLGG | 2 | 152425801 | 152425801 | + | Missense_Mutation | SNP | G | G | A | TCGA-VW-A7QS-01A-12D-A33T-08 | TCGA-VW-A7QS-10A-02D-A33W-08 | g.chr2:152425801G>A | c.12413C>T | c.(12412-12414)gCc>gTc | p.A4138V |
| GBMLGG | 2 | 152425820 | 152425820 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-1823-01A-01W-0643-08 | TCGA-14-1823-10A-01W-0644-08 | g.chr2:152425820C>T | c.12394G>A | c.(12394-12396)Gtc>Atc | p.V4132I |
| GBMLGG | 2 | 152470900 | 152470900 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-19-2623-01A-01D-1495-08 | TCGA-19-2623-10A-01D-1495-08 | g.chr2:152470900G>A | c.10762C>T | c.(10762-10764)Cag>Tag | p.Q3588* |
| GBMLGG | 2 | 152474871 | 152474871 | + | Missense_Mutation | SNP | C | C | T | TCGA-CS-5393-01A-01D-1468-08 | TCGA-CS-5393-10A-01D-1468-08 | g.chr2:152474871C>T | c.10265G>A | c.(10264-10266)cGt>cAt | p.R3422H |
| GBMLGG | 2 | 152476016 | 152476016 | + | Silent | SNP | G | G | A | TCGA-06-6391-01A-11D-1696-08 | TCGA-06-6391-10A-01D-1696-08 | g.chr2:152476016G>A | c.10092C>T | c.(10090-10092)ccC>ccT | p.P3364P |
| GBMLGG | 2 | 152476093 | 152476093 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152476093C>T | c.10015G>A | c.(10015-10017)Gtt>Att | p.V3339I |
| GBMLGG | 2 | 152477436 | 152477436 | + | Silent | SNP | A | A | G | TCGA-12-0616-01A-01D-1492-08 | TCGA-12-0616-10A-01D-1492-08 | g.chr2:152477436A>G | c.9828T>C | c.(9826-9828)agT>agC | p.S3276S |
| GBMLGG | 2 | 152483595 | 152483595 | + | Missense_Mutation | SNP | G | G | A | TCGA-DB-A64R-01A-11D-A29Q-08 | TCGA-DB-A64R-10A-01D-A29Q-08 | g.chr2:152483595G>A | c.9539C>T | c.(9538-9540)cCg>cTg | p.P3180L |
| GBMLGG | 2 | 152484105 | 152484105 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-1753-01A-01D-1494-08 | TCGA-28-1753-10B-01D-1494-08 | g.chr2:152484105C>T | c.9346G>A | c.(9346-9348)Gag>Aag | p.E3116K |
| GBMLGG | 2 | 152497084 | 152497084 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152497084C>T | c.8470G>A | c.(8470-8472)Gcc>Acc | p.A2824T |
| GBMLGG | 2 | 152497171 | 152497171 | + | Missense_Mutation | SNP | T | T | C | TCGA-DB-A64P-01A-11D-A29Q-08 | TCGA-DB-A64P-10A-01D-A29Q-08 | g.chr2:152497171T>C | c.8383A>G | c.(8383-8385)Aaa>Gaa | p.K2795E |
| GBMLGG | 2 | 152502668 | 152502668 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-QH-A65S-01A-11D-A29Q-08 | TCGA-QH-A65S-10A-01D-A29Q-08 | g.chr2:152502668delT | c.7512delA | c.(7510-7512)aaafs | p.K2504fs |
| GBMLGG | 2 | 152506778 | 152506778 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152506778C>T | c.7343G>A | c.(7342-7344)cGt>cAt | p.R2448H |
| GBMLGG | 2 | 152506786 | 152506786 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152506786C>A | c.7335G>T | c.(7333-7335)aaG>aaT | p.K2445N |
| GBMLGG | 2 | 152507377 | 152507377 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152507377C>T | c.6938G>A | c.(6937-6939)cGa>cAa | p.R2313Q |
| GBMLGG | 2 | 152518698 | 152518698 | + | Missense_Mutation | SNP | T | T | C | TCGA-19-2629-01A-01D-1495-08 | TCGA-19-2629-10A-01D-1495-08 | g.chr2:152518698T>C | c.5921A>G | c.(5920-5922)gAc>gGc | p.D1974G |
| GBMLGG | 2 | 152521900 | 152521900 | + | Missense_Mutation | SNP | T | T | A | TCGA-E1-5318-01A-01D-1468-08 | TCGA-E1-5318-10A-01D-1468-08 | g.chr2:152521900T>A | c.5185A>T | c.(5185-5187)Atg>Ttg | p.M1729L |
| GBMLGG | 2 | 152534196 | 152534196 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152534196G>A | c.3657C>T | c.(3655-3657)gcC>gcT | p.A1219A |
| GBMLGG | 2 | 152534214 | 152534214 | + | Silent | SNP | G | G | A | TCGA-HT-8111-01A-11D-2395-08 | TCGA-HT-8111-10A-01D-2396-08 | g.chr2:152534214G>A | c.3639C>T | c.(3637-3639)gtC>gtT | p.V1213V |
| GBMLGG | 2 | 152544001 | 152544004 | + | Frame_Shift_Del | DEL | CAAT | CAAT | - | TCGA-DU-7019-01A-11D-2024-08 | TCGA-DU-7019-10A-01D-2024-08 | g.chr2:152544001_152544004delCAAT | c.2566_2569delATTG | c.(2566-2571)attggafs | p.IG856fs |
| GBMLGG | 2 | 152580858 | 152580858 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-41-3392-01A-01D-1495-08 | TCGA-41-3392-10A-01D-1495-08 | g.chr2:152580858C>T | c.528G>A | c.(526-528)tgG>tgA | p.W176* |
| GBMLGG | 2 | 152581430 | 152581430 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152581430C>T | c.448G>A | c.(448-450)Gta>Ata | p.V150I |
| HNSC | 2 | 152348774 | 152348774 | + | Missense_Mutation | SNP | C | C | G | TCGA-RS-A6TO-01A-32D-A34J-08 | TCGA-RS-A6TO-10A-01D-A34M-08 | g.chr2:152348774C>G | c.19327G>C | c.(19327-19329)Gag>Cag | p.E6443Q |
| HNSC | 2 | 152363454 | 152363454 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-6012-01A-11D-1683-08 | TCGA-CN-6012-10A-01D-1683-08 | g.chr2:152363454C>T | c.18422G>A | c.(18421-18423)cGt>cAt | p.R6141H |
| HNSC | 2 | 152375496 | 152375496 | + | Missense_Mutation | SNP | T | T | G | TCGA-CV-6934-01A-11D-1912-08 | TCGA-CV-6934-10A-01D-1912-08 | g.chr2:152375496T>G | c.17575A>C | c.(17575-17577)Agc>Cgc | p.S5859R |
| HNSC | 2 | 152381070 | 152381070 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-6961-01A-21D-1912-08 | TCGA-CV-6961-10A-01D-1912-08 | g.chr2:152381070C>G | c.17230G>C | c.(17230-17232)Gac>Cac | p.D5744H |
| HNSC | 2 | 152383456 | 152383456 | + | Silent | SNP | G | G | C | TCGA-D6-A6ES-01A-12D-A31L-08 | TCGA-D6-A6ES-10A-01D-A31J-08 | g.chr2:152383456G>C | c.16818C>G | c.(16816-16818)ctC>ctG | p.L5606L |
| HNSC | 2 | 152383461 | 152383461 | + | Missense_Mutation | SNP | C | C | A | TCGA-CQ-5331-01A-02D-1870-08 | TCGA-CQ-5331-10A-01D-1870-08 | g.chr2:152383461C>A | c.16813G>T | c.(16813-16815)Gcc>Tcc | p.A5605S |
| HNSC | 2 | 152385794 | 152385794 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-6020-01A-11D-1683-08 | TCGA-CN-6020-10A-01D-1683-08 | g.chr2:152385794G>C | c.16562C>G | c.(16561-16563)tCc>tGc | p.S5521C |
| HNSC | 2 | 152394687 | 152394687 | + | Silent | SNP | G | G | C | TCGA-CQ-7071-01A-12D-A30E-08 | TCGA-CQ-7071-10A-01D-A30H-08 | g.chr2:152394687G>C | c.15861C>G | c.(15859-15861)gtC>gtG | p.V5287V |
| HNSC | 2 | 152397296 | 152397296 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-6956-01A-21D-2012-08 | TCGA-CV-6956-10A-01D-2013-08 | g.chr2:152397296G>T | c.15599C>A | c.(15598-15600)gCc>gAc | p.A5200D |
| HNSC | 2 | 152398013 | 152398013 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-6024-01A-11D-1683-08 | TCGA-CN-6024-10A-01D-1683-08 | g.chr2:152398013G>T | c.15527C>A | c.(15526-15528)cCt>cAt | p.P5176H |
| HNSC | 2 | 152398055 | 152398055 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7414-01A-11D-2078-08 | TCGA-CV-7414-10A-01D-2078-08 | g.chr2:152398055C>T | c.15485G>A | c.(15484-15486)aGa>aAa | p.R5162K |
| HNSC | 2 | 152417174 | 152417174 | + | Missense_Mutation | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr2:152417174T>C | c.14143A>G | c.(14143-14145)Agc>Ggc | p.S4715G |
| HNSC | 2 | 152419202 | 152419202 | + | Missense_Mutation | SNP | A | A | G | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr2:152419202A>G | c.13711T>C | c.(13711-13713)Tat>Cat | p.Y4571H |
| HNSC | 2 | 152420376 | 152420376 | + | Silent | SNP | G | G | T | TCGA-F7-A620-01A-11D-A28R-08 | TCGA-F7-A620-10A-01D-A28U-08 | g.chr2:152420376G>T | c.13437C>A | c.(13435-13437)ccC>ccA | p.P4479P |
| HNSC | 2 | 152423805 | 152423805 | + | Silent | SNP | G | G | A | TCGA-CV-7250-01A-11D-2012-08 | TCGA-CV-7250-10A-01D-2013-08 | g.chr2:152423805G>A | c.12930C>T | c.(12928-12930)gcC>gcT | p.A4310A |
| HNSC | 2 | 152423811 | 152423811 | + | Silent | SNP | G | G | C | TCGA-P3-A6T4-01A-11D-A34J-08 | TCGA-P3-A6T4-10A-01D-A34M-08 | g.chr2:152423811G>C | c.12924C>G | c.(12922-12924)gtC>gtG | p.V4308V |
| HNSC | 2 | 152423820 | 152423820 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-A461-01A-41D-A25Y-08 | TCGA-CV-A461-10A-01D-A25Y-08 | g.chr2:152423820C>A | c.12915G>T | c.(12913-12915)atG>atT | p.M4305I |
| HNSC | 2 | 152425879 | 152425879 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-A6JZ-01A-11D-A31L-08 | TCGA-CV-A6JZ-10A-01D-A31J-08 | g.chr2:152425879T>C | c.12335A>G | c.(12334-12336)tAc>tGc | p.Y4112C |
| HNSC | 2 | 152426612 | 152426612 | + | Missense_Mutation | SNP | A | A | C | TCGA-CV-7421-01A-11D-2078-08 | TCGA-CV-7421-10A-01D-2078-08 | g.chr2:152426612A>C | c.12310T>G | c.(12310-12312)Tac>Gac | p.Y4104D |
| HNSC | 2 | 152432252 | 152432252 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A45W-01A-11D-A25D-08 | TCGA-CV-A45W-10A-01D-A25E-08 | g.chr2:152432252G>A | c.11867C>T | c.(11866-11868)cCa>cTa | p.P3956L |
| HNSC | 2 | 152466344 | 152466345 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr2:152466344_152466345insT | c.11579_11580insA | c.(11578-11580)aagfs | p.K3860fs |
| HNSC | 2 | 152467061 | 152467062 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr2:152467061_152467062insT | c.11257_11258insA | c.(11257-11259)agtfs | p.S3753fs |
| HNSC | 2 | 152472608 | 152472608 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-A45W-01A-11D-A25D-08 | TCGA-CV-A45W-10A-01D-A25E-08 | g.chr2:152472608C>A | c.10468G>T | c.(10468-10470)Gct>Tct | p.A3490S |
| HNSC | 2 | 152483523 | 152483523 | + | Missense_Mutation | SNP | A | A | G | TCGA-CN-6016-01A-11D-1683-08 | TCGA-CN-6016-10A-01D-1683-08 | g.chr2:152483523A>G | c.9611T>C | c.(9610-9612)aTg>aCg | p.M3204T |
| HNSC | 2 | 152483591 | 152483591 | + | Missense_Mutation | SNP | G | G | C | TCGA-CV-7250-01A-11D-2012-08 | TCGA-CV-7250-10A-01D-2013-08 | g.chr2:152483591G>C | c.9543C>G | c.(9541-9543)gaC>gaG | p.D3181E |
| HNSC | 2 | 152486055 | 152486055 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-5432-01A-02D-1683-08 | TCGA-CV-5432-10A-01D-1870-08 | g.chr2:152486055C>A | c.9100G>T | c.(9100-9102)Gat>Tat | p.D3034Y |
| HNSC | 2 | 152490306 | 152490306 | + | Intron | SNP | C | C | A | TCGA-D6-A6EK-01A-11D-A31L-08 | TCGA-D6-A6EK-10A-01D-A31J-08 | g.chr2:152490306C>A | | | |
| HNSC | 2 | 152496975 | 152496975 | + | Missense_Mutation | SNP | G | G | A | TCGA-P3-A6T4-01A-11D-A34J-08 | TCGA-P3-A6T4-10A-01D-A34M-08 | g.chr2:152496975G>A | c.8579C>T | c.(8578-8580)aCc>aTc | p.T2860I |
| HNSC | 2 | 152497159 | 152497159 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr2:152497159G>A | c.8395C>T | c.(8395-8397)Cgt>Tgt | p.R2799C |
| HNSC | 2 | 152499769 | 152499769 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-6936-01A-11D-1912-08 | TCGA-CV-6936-10A-01D-1912-08 | g.chr2:152499769C>G | c.8055G>C | c.(8053-8055)ttG>ttC | p.L2685F |
| HNSC | 2 | 152500621 | 152500621 | + | Missense_Mutation | SNP | C | C | T | TCGA-IQ-A61J-01A-11D-A30E-08 | TCGA-IQ-A61J-10A-01D-A30H-08 | g.chr2:152500621C>T | c.7667G>A | c.(7666-7668)cGc>cAc | p.R2556H |
| HNSC | 2 | 152501079 | 152501079 | + | Missense_Mutation | SNP | C | C | A | TCGA-BB-4228-01A-01D-1434-08 | TCGA-BB-4228-10A-01D-1434-08 | g.chr2:152501079C>A | c.7547G>T | c.(7546-7548)cGa>cTa | p.R2516L |
| HNSC | 2 | 152507244 | 152507244 | + | Silent | SNP | G | G | A | TCGA-CR-6472-01A-11D-1870-08 | TCGA-CR-6472-10A-01D-1870-08 | g.chr2:152507244G>A | c.7071C>T | c.(7069-7071)ttC>ttT | p.F2357F |
| HNSC | 2 | 152512709 | 152512709 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7099-01A-41D-2012-08 | TCGA-CV-7099-10A-01D-2013-08 | g.chr2:152512709C>T | c.6453G>A | c.(6451-6453)atG>atA | p.M2151I |
| HNSC | 2 | 152512971 | 152512971 | + | Missense_Mutation | SNP | T | T | C | TCGA-CQ-6220-01A-11D-1912-08 | TCGA-CQ-6220-10A-01D-1912-08 | g.chr2:152512971T>C | c.6191A>G | c.(6190-6192)tAc>tGc | p.Y2064C |
| HNSC | 2 | 152518695 | 152518695 | + | Missense_Mutation | SNP | G | G | A | TCGA-D6-A6EN-01A-11D-A31L-08 | TCGA-D6-A6EN-10A-01D-A31J-08 | g.chr2:152518695G>A | c.5924C>T | c.(5923-5925)tCg>tTg | p.S1975L |
| HNSC | 2 | 152520126 | 152520126 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-7253-01A-11D-2012-08 | TCGA-CV-7253-10A-01D-2013-08 | g.chr2:152520126T>C | c.5699A>G | c.(5698-5700)tAc>tGc | p.Y1900C |
| HNSC | 2 | 152521102 | 152521102 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CR-7404-01A-11D-2129-08 | TCGA-CR-7404-10A-01D-2129-08 | g.chr2:152521102C>T | c.5364G>A | c.(5362-5364)tgG>tgA | p.W1788* |
| HNSC | 2 | 152522033 | 152522033 | + | Silent | SNP | G | G | A | TCGA-CN-A63Y-01A-11D-A30E-08 | TCGA-CN-A63Y-10A-01D-A30H-08 | g.chr2:152522033G>A | c.5052C>T | c.(5050-5052)ttC>ttT | p.F1684F |
| HNSC | 2 | 152534129 | 152534129 | + | Missense_Mutation | SNP | C | C | A | TCGA-CN-6997-01A-11D-2012-08 | TCGA-CN-6997-10A-01D-2013-08 | g.chr2:152534129C>A | c.3724G>T | c.(3724-3726)Gac>Tac | p.D1242Y |
| HNSC | 2 | 152534283 | 152534283 | + | Silent | SNP | G | G | A | TCGA-CV-7180-01A-11D-2012-08 | TCGA-CV-7180-10A-01D-2013-08 | g.chr2:152534283G>A | c.3570C>T | c.(3568-3570)aaC>aaT | p.N1190N |
| HNSC | 2 | 152534436 | 152534436 | + | Missense_Mutation | SNP | G | G | A | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr2:152534436G>A | c.3521C>T | c.(3520-3522)gCc>gTc | p.A1174V |
| HNSC | 2 | 152536301 | 152536301 | + | Silent | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr2:152536301T>C | c.3189A>G | c.(3187-3189)ggA>ggG | p.G1063G |
| HNSC | 2 | 152539188 | 152539188 | + | Silent | SNP | G | G | A | TCGA-CV-5977-01A-11D-1683-08 | TCGA-CV-5977-11A-01D-1683-08 | g.chr2:152539188G>A | c.2931C>T | c.(2929-2931)gaC>gaT | p.D977D |
| HNSC | 2 | 152539240 | 152539240 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7438-01A-21D-2129-08 | TCGA-CV-7438-10A-01D-2129-08 | g.chr2:152539240C>G | c.2879G>C | c.(2878-2880)gGc>gCc | p.G960A |
| HNSC | 2 | 152543963 | 152543963 | + | Missense_Mutation | SNP | G | G | C | TCGA-DQ-5631-01A-01D-1870-08 | TCGA-DQ-5631-10A-01D-1870-08 | g.chr2:152543963G>C | c.2607C>G | c.(2605-2607)caC>caG | p.H869Q |
| HNSC | 2 | 152548584 | 152548584 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-4723-01A-01D-1434-08 | TCGA-CN-4723-10A-01D-1434-08 | g.chr2:152548584G>C | c.2095C>G | c.(2095-2097)Caa>Gaa | p.Q699E |
| HNSC | 2 | 152563504 | 152563504 | + | Missense_Mutation | SNP | T | T | C | TCGA-BA-6869-01A-11D-1870-08 | TCGA-BA-6869-10A-01D-1870-08 | g.chr2:152563504T>C | c.1043A>G | c.(1042-1044)tAc>tGc | p.Y348C |
| HNSC | 2 | 152574009 | 152574009 | + | Missense_Mutation | SNP | T | T | C | TCGA-QK-A6IG-01A-11D-A31L-08 | TCGA-QK-A6IG-10A-01D-A31J-08 | g.chr2:152574009T>C | c.743A>G | c.(742-744)gAa>gGa | p.E248G |
| HNSC | 2 | 152580789 | 152580789 | + | Silent | SNP | G | G | A | TCGA-F7-A50J-01A-21D-A28R-08 | TCGA-F7-A50J-10A-01D-A28U-08 | g.chr2:152580789G>A | c.597C>T | c.(595-597)acC>acT | p.T199T |
| HNSC | 2 | 152580789 | 152580789 | + | Silent | SNP | G | G | C | TCGA-CN-5365-01A-01D-1434-08 | TCGA-CN-5365-10A-01D-1434-08 | g.chr2:152580789G>C | c.597C>G | c.(595-597)acC>acG | p.T199T |
| HNSC | 2 | 152586143 | 152586143 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7091-01A-11D-2012-08 | TCGA-CV-7091-10A-01D-2013-08 | g.chr2:152586143C>T | c.64G>A | c.(64-66)Gag>Aag | p.E22K |
| KICH | 2 | 152350685 | 152350685 | + | Missense_Mutation | SNP | T | T | C | TCGA-KL-8323-01A-21D-2310-10 | TCGA-KL-8323-11A-01D-2310-10 | g.chr2:152350685T>C | c.19001A>G | c.(19000-19002)aAc>aGc | p.N6334S |
| KIPAN | 2 | 152346999 | 152346999 | + | Missense_Mutation | SNP | C | C | T | TCGA-B0-5095-01A-01D-1421-08 | TCGA-B0-5095-11A-01D-1421-08 | g.chr2:152346999C>T | c.19616G>A | c.(19615-19617)cGa>cAa | p.R6539Q |
| KIPAN | 2 | 152347020 | 152347020 | + | Missense_Mutation | SNP | C | C | A | TCGA-AK-3454-01A-02D-1361-10 | TCGA-AK-3454-10A-01D-1361-10 | g.chr2:152347020C>A | c.19595G>T | c.(19594-19596)cGc>cTc | p.R6532L |
| KIPAN | 2 | 152348619 | 152348619 | + | Silent | SNP | A | A | C | TCGA-B2-3924-01A-02D-1386-10 | TCGA-B2-3924-11A-01D-1251-10 | g.chr2:152348619A>C | c.19482T>G | c.(19480-19482)acT>acG | p.T6494T |
| KIPAN | 2 | 152350685 | 152350685 | + | Missense_Mutation | SNP | T | T | C | TCGA-KL-8323-01A-21D-2310-10 | TCGA-KL-8323-11A-01D-2310-10 | g.chr2:152350685T>C | c.19001A>G | c.(19000-19002)aAc>aGc | p.N6334S |
| KIPAN | 2 | 152352797 | 152352797 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-5107-01A-01D-1421-08 | TCGA-B0-5107-11A-01D-1421-08 | g.chr2:152352797A>G | c.18911T>C | c.(18910-18912)aTt>aCt | p.I6304T |
| KIPAN | 2 | 152359933 | 152359933 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-Y8-A8S0-01A-11D-A36X-10 | TCGA-Y8-A8S0-10A-01D-A370-10 | g.chr2:152359933delC | c.18662delG | c.(18661-18663)ggafs | p.G6221fs |
| KIPAN | 2 | 152362014 | 152362014 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-BP-4967-01A-01D-1462-08 | TCGA-BP-4967-11A-01D-1462-08 | g.chr2:152362014delT | c.18617delA | c.(18616-18618)gagfs | p.E6206fs |
| KIPAN | 2 | 152382499 | 152382499 | + | Silent | SNP | G | G | A | TCGA-IZ-A6M9-01A-11D-A31X-10 | TCGA-IZ-A6M9-10A-01D-A31X-10 | g.chr2:152382499G>A | c.17031C>T | c.(17029-17031)gtC>gtT | p.V5677V |
| KIPAN | 2 | 152390040 | 152390040 | + | Intron | SNP | G | G | T | TCGA-GL-A59R-01A-11D-A26P-10 | TCGA-GL-A59R-10A-01D-A26P-10 | g.chr2:152390040G>T | | | |
| KIPAN | 2 | 152397301 | 152397301 | + | Silent | SNP | T | T | C | TCGA-CJ-4905-01A-02D-1429-08 | TCGA-CJ-4905-11A-01D-1429-08 | g.chr2:152397301T>C | c.15594A>G | c.(15592-15594)gaA>gaG | p.E5198E |
| KIPAN | 2 | 152410531 | 152410531 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-2Z-A9JO-01A-11D-A42J-10 | TCGA-2Z-A9JO-10A-01D-A42M-10 | g.chr2:152410531G>T | c.14334C>A | c.(14332-14334)taC>taA | p.Y4778* |
| KIPAN | 2 | 152467134 | 152467134 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-4761-01A-01D-1366-10 | TCGA-BP-4761-11A-01D-1366-10 | g.chr2:152467134G>T | c.11185C>A | c.(11185-11187)Ctt>Att | p.L3729I |
| KIPAN | 2 | 152471015 | 152471015 | + | Silent | SNP | G | G | T | TCGA-B4-5835-01A-11D-1669-08 | TCGA-B4-5835-10A-01D-1669-08 | g.chr2:152471015G>T | c.10647C>A | c.(10645-10647)tcC>tcA | p.S3549S |
| KIPAN | 2 | 152476170 | 152476170 | + | Missense_Mutation | SNP | T | T | C | TCGA-B0-5701-01A-11D-1534-10 | TCGA-B0-5701-11A-01D-1534-10 | g.chr2:152476170T>C | c.9938A>G | c.(9937-9939)cAg>cGg | p.Q3313R |
| KIPAN | 2 | 152482148 | 152482148 | + | Missense_Mutation | SNP | A | A | G | TCGA-A4-8310-01A-11D-2396-08 | TCGA-A4-8310-10A-01D-2396-08 | g.chr2:152482148A>G | c.9623T>C | c.(9622-9624)tTa>tCa | p.L3208S |
| KIPAN | 2 | 152507333 | 152507333 | + | Missense_Mutation | SNP | C | C | T | TCGA-B9-7268-01A-11D-2136-08 | TCGA-B9-7268-10A-01D-2136-08 | g.chr2:152507333C>T | c.6982G>A | c.(6982-6984)Gac>Aac | p.D2328N |
| KIPAN | 2 | 152512859 | 152512859 | + | Silent | SNP | C | C | T | TCGA-DW-5560-01A-01D-1589-08 | TCGA-DW-5560-10A-01D-1589-08 | g.chr2:152512859C>T | c.6303G>A | c.(6301-6303)gaG>gaA | p.E2101E |
| KIPAN | 2 | 152522655 | 152522655 | + | Silent | SNP | G | G | T | TCGA-G7-6795-01A-11D-1961-08 | TCGA-G7-6795-10A-01D-1962-08 | g.chr2:152522655G>T | c.4980C>A | c.(4978-4980)ccC>ccA | p.P1660P |
| KIPAN | 2 | 152529113 | 152529113 | + | Missense_Mutation | SNP | G | G | T | TCGA-B0-5102-01A-01D-1421-08 | TCGA-B0-5102-11A-01D-1421-08 | g.chr2:152529113G>T | c.4069C>A | c.(4069-4071)Cac>Aac | p.H1357N |
| KIPAN | 2 | 152534241 | 152534241 | + | Silent | SNP | G | G | C | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr2:152534241G>C | c.3612C>G | c.(3610-3612)ggC>ggG | p.G1204G |
| KIPAN | 2 | 152548582 | 152548582 | + | Silent | SNP | T | T | C | TCGA-BP-5000-01A-01D-1462-08 | TCGA-BP-5000-11A-01D-1462-08 | g.chr2:152548582T>C | c.2097A>G | c.(2095-2097)caA>caG | p.Q699Q |
| KIPAN | 2 | 152551064 | 152551064 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-5182-01A-01D-1429-08 | TCGA-BP-5182-11A-01D-1429-08 | g.chr2:152551064G>T | c.1754C>A | c.(1753-1755)gCc>gAc | p.A585D |
| KIPAN | 2 | 152552137 | 152552137 | + | Silent | SNP | A | A | T | TCGA-BP-4174-01A-02D-1366-10 | TCGA-BP-4174-11A-01D-1366-10 | g.chr2:152552137A>T | c.1629T>A | c.(1627-1629)acT>acA | p.T543T |
| KIPAN | 2 | 152553192 | 152553192 | + | Missense_Mutation | SNP | C | C | A | TCGA-CZ-5467-01A-01D-1501-10 | TCGA-CZ-5467-11A-01D-1501-10 | g.chr2:152553192C>A | c.1528G>T | c.(1528-1530)Gtt>Ttt | p.V510F |
| KIPAN | 2 | 152554080 | 152554080 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-4693-01A-01D-1361-10 | TCGA-B0-4693-11A-01D-1361-10 | g.chr2:152554080A>G | c.1235T>C | c.(1234-1236)gTt>gCt | p.V412A |
| KIPAN | 2 | 152579988 | 152579989 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AT-A5NU-01A-11D-A28G-10 | TCGA-AT-A5NU-10A-01D-A28G-10 | g.chr2:152579988_152579989insA | c.624_625insT | c.(622-627)actgaafs | p.E209fs |
| KIRC | 2 | 152346999 | 152346999 | + | Missense_Mutation | SNP | C | C | T | TCGA-B0-5095-01A-01D-1421-08 | TCGA-B0-5095-11A-01D-1421-08 | g.chr2:152346999C>T | c.19616G>A | c.(19615-19617)cGa>cAa | p.R6539Q |
| KIRC | 2 | 152347020 | 152347020 | + | Missense_Mutation | SNP | C | C | A | TCGA-AK-3454-01A-02D-1361-10 | TCGA-AK-3454-10A-01D-1361-10 | g.chr2:152347020C>A | c.19595G>T | c.(19594-19596)cGc>cTc | p.R6532L |
| KIRC | 2 | 152348619 | 152348619 | + | Silent | SNP | A | A | C | TCGA-B2-3924-01A-02D-1386-10 | TCGA-B2-3924-11A-01D-1251-10 | g.chr2:152348619A>C | c.19482T>G | c.(19480-19482)acT>acG | p.T6494T |
| KIRC | 2 | 152352797 | 152352797 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-5107-01A-01D-1421-08 | TCGA-B0-5107-11A-01D-1421-08 | g.chr2:152352797A>G | c.18911T>C | c.(18910-18912)aTt>aCt | p.I6304T |
| KIRC | 2 | 152362014 | 152362014 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-BP-4967-01A-01D-1462-08 | TCGA-BP-4967-11A-01D-1462-08 | g.chr2:152362014delT | c.18617delA | c.(18616-18618)gagfs | p.E6206fs |
| KIRC | 2 | 152397301 | 152397301 | + | Silent | SNP | T | T | C | TCGA-CJ-4905-01A-02D-1429-08 | TCGA-CJ-4905-11A-01D-1429-08 | g.chr2:152397301T>C | c.15594A>G | c.(15592-15594)gaA>gaG | p.E5198E |
| KIRC | 2 | 152467134 | 152467134 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-4761-01A-01D-1366-10 | TCGA-BP-4761-11A-01D-1366-10 | g.chr2:152467134G>T | c.11185C>A | c.(11185-11187)Ctt>Att | p.L3729I |
| KIRC | 2 | 152471015 | 152471015 | + | Silent | SNP | G | G | T | TCGA-B4-5835-01A-11D-1669-08 | TCGA-B4-5835-10A-01D-1669-08 | g.chr2:152471015G>T | c.10647C>A | c.(10645-10647)tcC>tcA | p.S3549S |
| KIRC | 2 | 152476170 | 152476170 | + | Missense_Mutation | SNP | T | T | C | TCGA-B0-5701-01A-11D-1534-10 | TCGA-B0-5701-11A-01D-1534-10 | g.chr2:152476170T>C | c.9938A>G | c.(9937-9939)cAg>cGg | p.Q3313R |
| KIRC | 2 | 152529113 | 152529113 | + | Missense_Mutation | SNP | G | G | T | TCGA-B0-5102-01A-01D-1421-08 | TCGA-B0-5102-11A-01D-1421-08 | g.chr2:152529113G>T | c.4069C>A | c.(4069-4071)Cac>Aac | p.H1357N |
| KIRC | 2 | 152534241 | 152534241 | + | Silent | SNP | G | G | C | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr2:152534241G>C | c.3612C>G | c.(3610-3612)ggC>ggG | p.G1204G |
| KIRC | 2 | 152548582 | 152548582 | + | Silent | SNP | T | T | C | TCGA-BP-5000-01A-01D-1462-08 | TCGA-BP-5000-11A-01D-1462-08 | g.chr2:152548582T>C | c.2097A>G | c.(2095-2097)caA>caG | p.Q699Q |
| KIRC | 2 | 152551064 | 152551064 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-5182-01A-01D-1429-08 | TCGA-BP-5182-11A-01D-1429-08 | g.chr2:152551064G>T | c.1754C>A | c.(1753-1755)gCc>gAc | p.A585D |
| KIRC | 2 | 152552137 | 152552137 | + | Silent | SNP | A | A | T | TCGA-BP-4174-01A-02D-1366-10 | TCGA-BP-4174-11A-01D-1366-10 | g.chr2:152552137A>T | c.1629T>A | c.(1627-1629)acT>acA | p.T543T |
| KIRC | 2 | 152553192 | 152553192 | + | Missense_Mutation | SNP | C | C | A | TCGA-CZ-5467-01A-01D-1501-10 | TCGA-CZ-5467-11A-01D-1501-10 | g.chr2:152553192C>A | c.1528G>T | c.(1528-1530)Gtt>Ttt | p.V510F |
| KIRC | 2 | 152554080 | 152554080 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-4693-01A-01D-1361-10 | TCGA-B0-4693-11A-01D-1361-10 | g.chr2:152554080A>G | c.1235T>C | c.(1234-1236)gTt>gCt | p.V412A |
| KIRP | 2 | 152359933 | 152359933 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-Y8-A8S0-01A-11D-A36X-10 | TCGA-Y8-A8S0-10A-01D-A370-10 | g.chr2:152359933delC | c.18662delG | c.(18661-18663)ggafs | p.G6221fs |
| KIRP | 2 | 152382499 | 152382499 | + | Silent | SNP | G | G | A | TCGA-IZ-A6M9-01A-11D-A31X-10 | TCGA-IZ-A6M9-10A-01D-A31X-10 | g.chr2:152382499G>A | c.17031C>T | c.(17029-17031)gtC>gtT | p.V5677V |
| KIRP | 2 | 152390040 | 152390040 | + | Intron | SNP | G | G | T | TCGA-GL-A59R-01A-11D-A26P-10 | TCGA-GL-A59R-10A-01D-A26P-10 | g.chr2:152390040G>T | | | |
| KIRP | 2 | 152410531 | 152410531 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-2Z-A9JO-01A-11D-A42J-10 | TCGA-2Z-A9JO-10A-01D-A42M-10 | g.chr2:152410531G>T | c.14334C>A | c.(14332-14334)taC>taA | p.Y4778* |
| KIRP | 2 | 152482148 | 152482148 | + | Missense_Mutation | SNP | A | A | G | TCGA-A4-8310-01A-11D-2396-08 | TCGA-A4-8310-10A-01D-2396-08 | g.chr2:152482148A>G | c.9623T>C | c.(9622-9624)tTa>tCa | p.L3208S |
| KIRP | 2 | 152507333 | 152507333 | + | Missense_Mutation | SNP | C | C | T | TCGA-B9-7268-01A-11D-2136-08 | TCGA-B9-7268-10A-01D-2136-08 | g.chr2:152507333C>T | c.6982G>A | c.(6982-6984)Gac>Aac | p.D2328N |
| KIRP | 2 | 152512859 | 152512859 | + | Silent | SNP | C | C | T | TCGA-DW-5560-01A-01D-1589-08 | TCGA-DW-5560-10A-01D-1589-08 | g.chr2:152512859C>T | c.6303G>A | c.(6301-6303)gaG>gaA | p.E2101E |
| KIRP | 2 | 152522655 | 152522655 | + | Silent | SNP | G | G | T | TCGA-G7-6795-01A-11D-1961-08 | TCGA-G7-6795-10A-01D-1962-08 | g.chr2:152522655G>T | c.4980C>A | c.(4978-4980)ccC>ccA | p.P1660P |
| KIRP | 2 | 152579988 | 152579989 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AT-A5NU-01A-11D-A28G-10 | TCGA-AT-A5NU-10A-01D-A28G-10 | g.chr2:152579988_152579989insA | c.624_625insT | c.(622-627)actgaafs | p.E209fs |
| LAML | 2 | 152419193 | 152419193 | + | Missense_Mutation | SNP | G | G | T | TCGA-AB-2871-03A-01W-0732-08 | TCGA-AB-2871-11A-01W-0732-08 | g.chr2:152419193G>T | c.13720C>A | c.(13720-13722)Cag>Aag | p.Q4574K |
| LGG | 2 | 152342397 | 152342397 | + | Silent | SNP | C | C | T | TCGA-DH-5142-01A-01D-1468-08 | TCGA-DH-5142-10A-01D-1468-08 | g.chr2:152342397C>T | c.19887G>A | c.(19885-19887)gtG>gtA | p.V6629V |
| LGG | 2 | 152374910 | 152374910 | + | Missense_Mutation | SNP | C | C | G | TCGA-E1-5307-01A-01D-1893-08 | TCGA-E1-5307-10A-01D-1893-08 | g.chr2:152374910C>G | c.17619G>C | c.(17617-17619)aaG>aaC | p.K5873N |
| LGG | 2 | 152376199 | 152376199 | + | Missense_Mutation | SNP | C | C | T | TCGA-E1-5307-01A-01D-1893-08 | TCGA-E1-5307-10A-01D-1893-08 | g.chr2:152376199C>T | c.17460G>A | c.(17458-17460)atG>atA | p.M5820I |
| LGG | 2 | 152383461 | 152383461 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-7301-01A-11D-2086-08 | TCGA-DU-7301-10A-01D-2086-08 | g.chr2:152383461C>T | c.16813G>A | c.(16813-16815)Gcc>Acc | p.A5605T |
| LGG | 2 | 152406213 | 152406213 | + | Silent | SNP | A | A | G | TCGA-DB-5273-01A-01D-1468-08 | TCGA-DB-5273-10A-01D-1468-08 | g.chr2:152406213A>G | c.14883T>C | c.(14881-14883)taT>taC | p.Y4961Y |
| LGG | 2 | 152409920 | 152409920 | + | Missense_Mutation | SNP | G | G | A | TCGA-CS-5396-01A-02D-1468-08 | TCGA-CS-5396-10A-01D-1468-08 | g.chr2:152409920G>A | c.14620C>T | c.(14620-14622)Cgt>Tgt | p.R4874C |
| LGG | 2 | 152409936 | 152409936 | + | Silent | SNP | C | C | T | TCGA-P5-A5ET-01A-11D-A27K-08 | TCGA-P5-A5ET-10A-01D-A27N-08 | g.chr2:152409936C>T | c.14604G>A | c.(14602-14604)aaG>aaA | p.K4868K |
| LGG | 2 | 152410491 | 152410491 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152410491C>T | c.14374G>A | c.(14374-14376)Gtg>Atg | p.V4792M |
| LGG | 2 | 152420364 | 152420364 | + | Silent | SNP | G | G | A | TCGA-TQ-A7RN-01A-11D-A33T-08 | TCGA-TQ-A7RN-10A-01D-A33W-08 | g.chr2:152420364G>A | c.13449C>T | c.(13447-13449)gcC>gcT | p.A4483A |
| LGG | 2 | 152422294 | 152422294 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152422294C>T | c.13094G>A | c.(13093-13095)gGc>gAc | p.G4365D |
| LGG | 2 | 152423688 | 152423688 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152423688C>A | c.13047G>T | c.(13045-13047)caG>caT | p.Q4349H |
| LGG | 2 | 152425801 | 152425801 | + | Missense_Mutation | SNP | G | G | A | TCGA-VW-A7QS-01A-12D-A33T-08 | TCGA-VW-A7QS-10A-02D-A33W-08 | g.chr2:152425801G>A | c.12413C>T | c.(12412-12414)gCc>gTc | p.A4138V |
| LGG | 2 | 152474871 | 152474871 | + | Missense_Mutation | SNP | C | C | T | TCGA-CS-5393-01A-01D-1468-08 | TCGA-CS-5393-10A-01D-1468-08 | g.chr2:152474871C>T | c.10265G>A | c.(10264-10266)cGt>cAt | p.R3422H |
| LGG | 2 | 152476093 | 152476093 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152476093C>T | c.10015G>A | c.(10015-10017)Gtt>Att | p.V3339I |
| LGG | 2 | 152483595 | 152483595 | + | Missense_Mutation | SNP | G | G | A | TCGA-DB-A64R-01A-11D-A29Q-08 | TCGA-DB-A64R-10A-01D-A29Q-08 | g.chr2:152483595G>A | c.9539C>T | c.(9538-9540)cCg>cTg | p.P3180L |
| LGG | 2 | 152497084 | 152497084 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152497084C>T | c.8470G>A | c.(8470-8472)Gcc>Acc | p.A2824T |
| LGG | 2 | 152497171 | 152497171 | + | Missense_Mutation | SNP | T | T | C | TCGA-DB-A64P-01A-11D-A29Q-08 | TCGA-DB-A64P-10A-01D-A29Q-08 | g.chr2:152497171T>C | c.8383A>G | c.(8383-8385)Aaa>Gaa | p.K2795E |
| LGG | 2 | 152502668 | 152502668 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-QH-A65S-01A-11D-A29Q-08 | TCGA-QH-A65S-10A-01D-A29Q-08 | g.chr2:152502668delT | c.7512delA | c.(7510-7512)aaafs | p.K2504fs |
| LGG | 2 | 152506778 | 152506778 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152506778C>T | c.7343G>A | c.(7342-7344)cGt>cAt | p.R2448H |
| LGG | 2 | 152506786 | 152506786 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152506786C>A | c.7335G>T | c.(7333-7335)aaG>aaT | p.K2445N |
| LGG | 2 | 152507377 | 152507377 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152507377C>T | c.6938G>A | c.(6937-6939)cGa>cAa | p.R2313Q |
| LGG | 2 | 152521900 | 152521900 | + | Missense_Mutation | SNP | T | T | A | TCGA-E1-5318-01A-01D-1468-08 | TCGA-E1-5318-10A-01D-1468-08 | g.chr2:152521900T>A | c.5185A>T | c.(5185-5187)Atg>Ttg | p.M1729L |
| LGG | 2 | 152534196 | 152534196 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152534196G>A | c.3657C>T | c.(3655-3657)gcC>gcT | p.A1219A |
| LGG | 2 | 152534214 | 152534214 | + | Silent | SNP | G | G | A | TCGA-HT-8111-01A-11D-2395-08 | TCGA-HT-8111-10A-01D-2396-08 | g.chr2:152534214G>A | c.3639C>T | c.(3637-3639)gtC>gtT | p.V1213V |
| LGG | 2 | 152544001 | 152544004 | + | Frame_Shift_Del | DEL | CAAT | CAAT | - | TCGA-DU-7019-01A-11D-2024-08 | TCGA-DU-7019-10A-01D-2024-08 | g.chr2:152544001_152544004delCAAT | c.2566_2569delATTG | c.(2566-2571)attggafs | p.IG856fs |
| LGG | 2 | 152581430 | 152581430 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:152581430C>T | c.448G>A | c.(448-450)Gta>Ata | p.V150I |
| LIHC | 2 | 152350375 | 152350375 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-AAEA-01A-11D-A40R-10 | TCGA-DD-AAEA-10A-01D-A40U-10 | g.chr2:152350375A>G | c.19018T>C | c.(19018-19020)Tac>Cac | p.Y6340H |
| LIHC | 2 | 152392260 | 152392260 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-A39Z-01A-11D-A20W-10 | TCGA-DD-A39Z-11A-21D-A20W-10 | g.chr2:152392260A>G | c.16154T>C | c.(16153-16155)gTt>gCt | p.V5385A |
| LIHC | 2 | 152402893 | 152402893 | + | Missense_Mutation | SNP | T | T | C | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr2:152402893T>C | c.15329A>G | c.(15328-15330)gAc>gGc | p.D5110G |
| LIHC | 2 | 152424933 | 152424933 | + | Splice_Site | SNP | T | T | A | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr2:152424933T>A | | c.e84-2 | |
| LIHC | 2 | 152426620 | 152426620 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-AAVR-01A-11D-A40R-10 | TCGA-DD-AAVR-10A-01D-A40U-10 | g.chr2:152426620delT | c.12302delA | c.(12301-12303)aagfs | p.K4102fs |
| LIHC | 2 | 152466364 | 152466364 | + | Missense_Mutation | SNP | C | C | G | TCGA-FV-A496-01A-11D-A25V-10 | TCGA-FV-A496-10A-01D-A25V-10 | g.chr2:152466364C>G | c.11560G>C | c.(11560-11562)Gac>Cac | p.D3854H |
| LIHC | 2 | 152466364 | 152466364 | + | Missense_Mutation | SNP | C | C | G | TCGA-G3-A3CI-01A-11D-A20W-10 | TCGA-G3-A3CI-10A-01D-A20W-10 | g.chr2:152466364C>G | c.11560G>C | c.(11560-11562)Gac>Cac | p.D3854H |
| LIHC | 2 | 152466569 | 152466569 | + | Silent | SNP | A | A | G | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr2:152466569A>G | c.11355T>C | c.(11353-11355)gaT>gaC | p.D3785D |
| LIHC | 2 | 152467281 | 152467281 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr2:152467281delT | c.11176delA | c.(11176-11178)agcfs | p.S3726fs |
| LIHC | 2 | 152473927 | 152473927 | + | Missense_Mutation | SNP | T | T | A | TCGA-ZP-A9D1-01A-11D-A382-10 | TCGA-ZP-A9D1-10B-01D-A385-10 | g.chr2:152473927T>A | c.10403A>T | c.(10402-10404)gAt>gTt | p.D3468V |
| LIHC | 2 | 152497166 | 152497166 | + | Missense_Mutation | SNP | T | T | G | TCGA-QA-A7B7-01A-11D-A32G-10 | TCGA-QA-A7B7-10A-01D-A32G-10 | g.chr2:152497166T>G | c.8388A>C | c.(8386-8388)gaA>gaC | p.E2796D |
| LIHC | 2 | 152499357 | 152499357 | + | Silent | SNP | T | T | C | TCGA-RC-A7SB-01A-21D-A34Z-10 | TCGA-RC-A7SB-10A-01D-A34Z-10 | g.chr2:152499357T>C | c.8187A>G | c.(8185-8187)aaA>aaG | p.K2729K |
| LIHC | 2 | 152506778 | 152506778 | + | Missense_Mutation | SNP | C | C | T | TCGA-DD-A4ND-01A-11D-A25V-10 | TCGA-DD-A4ND-11A-11D-A25V-10 | g.chr2:152506778C>T | c.7343G>A | c.(7342-7344)cGt>cAt | p.R2448H |
| LIHC | 2 | 152512686 | 152512686 | + | Missense_Mutation | SNP | A | A | G | TCGA-CC-A7IK-01A-12D-A33Q-10 | TCGA-CC-A7IK-10A-01D-A33Q-10 | g.chr2:152512686A>G | c.6476T>C | c.(6475-6477)aTg>aCg | p.M2159T |
| LIHC | 2 | 152522831 | 152522831 | + | Missense_Mutation | SNP | A | A | T | TCGA-CC-A7IH-01A-11D-A33K-10 | TCGA-CC-A7IH-10A-01D-A33K-10 | g.chr2:152522831A>T | c.4804T>A | c.(4804-4806)Tac>Aac | p.Y1602N |
| LIHC | 2 | 152528994 | 152528994 | + | Silent | SNP | G | G | T | TCGA-HP-A5N0-01A-11D-A28X-10 | TCGA-HP-A5N0-10A-01D-A28X-10 | g.chr2:152528994G>T | c.4188C>A | c.(4186-4188)gcC>gcA | p.A1396A |
| LIHC | 2 | 152529088 | 152529088 | + | Missense_Mutation | SNP | T | T | A | TCGA-DD-AACK-01A-11D-A40R-10 | TCGA-DD-AACK-10A-01D-A40U-10 | g.chr2:152529088T>A | c.4094A>T | c.(4093-4095)cAg>cTg | p.Q1365L |
| LIHC | 2 | 152534508 | 152534508 | + | Missense_Mutation | SNP | T | T | A | TCGA-ZP-A9D1-01A-11D-A382-10 | TCGA-ZP-A9D1-10B-01D-A385-10 | g.chr2:152534508T>A | c.3449A>T | c.(3448-3450)aAg>aTg | p.K1150M |
| LIHC | 2 | 152534626 | 152534626 | + | Silent | SNP | G | G | A | TCGA-DD-A39Z-01A-11D-A20W-10 | TCGA-DD-A39Z-11A-21D-A20W-10 | g.chr2:152534626G>A | c.3331C>T | c.(3331-3333)Ctg>Ttg | p.L1111L |
| LIHC | 2 | 152539201 | 152539201 | + | Missense_Mutation | SNP | T | T | A | TCGA-CC-A5UD-01A-11D-A28X-10 | TCGA-CC-A5UD-10A-01D-A28X-10 | g.chr2:152539201T>A | c.2918A>T | c.(2917-2919)aAg>aTg | p.K973M |
| LIHC | 2 | 152552146 | 152552146 | + | Silent | SNP | G | G | C | TCGA-DD-A11A-01A-11D-A12Z-10 | TCGA-DD-A11A-10A-01D-A12Z-10 | g.chr2:152552146G>C | c.1620C>G | c.(1618-1620)ccC>ccG | p.P540P |
| LIHC | 2 | 152581406 | 152581406 | + | Missense_Mutation | SNP | C | C | T | TCGA-DD-AAEI-01A-11D-A40R-10 | TCGA-DD-AAEI-10A-01D-A40U-10 | g.chr2:152581406C>T | c.472G>A | c.(472-474)Gaa>Aaa | p.E158K |
| LUAD | 2 | 152348631 | 152348631 | + | Missense_Mutation | SNP | T | T | A | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr2:152348631T>A | c.19470A>T | c.(19468-19470)caA>caT | p.Q6490H |
| LUAD | 2 | 152361993 | 152361993 | + | Splice_Site | SNP | G | G | T | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr2:152361993G>T | c.18638C>A | c.(18637-18639)tCg>tAg | p.S6213* |
| LUAD | 2 | 152362721 | 152362721 | + | Missense_Mutation | SNP | C | C | T | TCGA-50-5946-01A-11D-1753-08 | TCGA-50-5946-10A-01D-1753-08 | g.chr2:152362721C>T | c.18505G>A | c.(18505-18507)Gag>Aag | p.E6169K |
| LUAD | 2 | 152363473 | 152363473 | + | Missense_Mutation | SNP | C | C | T | TCGA-73-7499-01A-11D-2184-08 | TCGA-73-7499-10A-01D-2184-08 | g.chr2:152363473C>T | c.18403G>A | c.(18403-18405)Gac>Aac | p.D6135N |
| LUAD | 2 | 152381116 | 152381117 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr2:152381116_152381117delTT | c.17183_17184delAA | c.(17182-17184)aaafs | p.K5728fs |
| LUAD | 2 | 152383524 | 152383524 | + | Missense_Mutation | SNP | G | G | T | TCGA-91-6849-01A-11D-1945-08 | TCGA-91-6849-11A-01D-1945-08 | g.chr2:152383524G>T | c.16750C>A | c.(16750-16752)Ctg>Atg | p.L5584M |
| LUAD | 2 | 152387542 | 152387542 | + | Missense_Mutation | SNP | A | A | T | TCGA-44-2657-01A-01D-1105-08 | TCGA-44-2657-10A-01D-1105-08 | g.chr2:152387542A>T | c.16493T>A | c.(16492-16494)cTg>cAg | p.L5498Q |
| LUAD | 2 | 152394467 | 152394467 | + | Missense_Mutation | SNP | C | C | G | TCGA-44-A47A-01A-21D-A24D-08 | TCGA-44-A47A-10A-01D-A24F-08 | g.chr2:152394467C>G | c.15918G>C | c.(15916-15918)atG>atC | p.M5306I |
| LUAD | 2 | 152404226 | 152404226 | + | Missense_Mutation | SNP | T | T | A | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr2:152404226T>A | c.15081A>T | c.(15079-15081)aaA>aaT | p.K5027N |
| LUAD | 2 | 152404840 | 152404840 | + | Silent | SNP | G | G | T | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr2:152404840G>T | c.15036C>A | c.(15034-15036)gtC>gtA | p.V5012V |
| LUAD | 2 | 152406213 | 152406213 | + | Silent | SNP | A | A | G | TCGA-55-8301-01A-11D-2284-08 | TCGA-55-8301-10A-01D-2284-08 | g.chr2:152406213A>G | c.14883T>C | c.(14881-14883)taT>taC | p.Y4961Y |
| LUAD | 2 | 152408338 | 152408338 | + | Missense_Mutation | SNP | C | C | A | TCGA-97-7937-01A-11D-2167-08 | TCGA-97-7937-10A-01D-2167-08 | g.chr2:152408338C>A | c.14755G>T | c.(14755-14757)Gtg>Ttg | p.V4919L |
| LUAD | 2 | 152410453 | 152410453 | + | Silent | SNP | G | G | C | TCGA-86-8672-01A-21D-2393-08 | TCGA-86-8672-10A-01D-2393-08 | g.chr2:152410453G>C | c.14412C>G | c.(14410-14412)tcC>tcG | p.S4804S |
| LUAD | 2 | 152410462 | 152410462 | + | Silent | SNP | G | G | T | TCGA-05-4398-01A-01D-1265-08 | TCGA-05-4398-10A-01D-1265-08 | g.chr2:152410462G>T | c.14403C>A | c.(14401-14403)gcC>gcA | p.A4801A |
| LUAD | 2 | 152410485 | 152410485 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr2:152410485C>A | c.14380G>T | c.(14380-14382)Gac>Tac | p.D4794Y |
| LUAD | 2 | 152417107 | 152417107 | + | Splice_Site | SNP | T | T | C | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr2:152417107T>C | c.14210A>G | c.(14209-14211)cAt>cGt | p.H4737R |
| LUAD | 2 | 152417530 | 152417530 | + | Silent | SNP | A | A | G | TCGA-95-A4VP-01A-21D-A25L-08 | TCGA-95-A4VP-10A-01D-A25L-08 | g.chr2:152417530A>G | c.14091T>C | c.(14089-14091)aaT>aaC | p.N4697N |
| LUAD | 2 | 152419190 | 152419190 | + | Missense_Mutation | SNP | A | A | C | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr2:152419190A>C | c.13723T>G | c.(13723-13725)Tgg>Ggg | p.W4575G |
| LUAD | 2 | 152420221 | 152420221 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr2:152420221C>G | c.13489G>C | c.(13489-13491)Gag>Cag | p.E4497Q |
| LUAD | 2 | 152422283 | 152422283 | + | Missense_Mutation | SNP | G | G | C | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr2:152422283G>C | c.13105C>G | c.(13105-13107)Ctg>Gtg | p.L4369V |
| LUAD | 2 | 152423688 | 152423688 | + | Silent | SNP | C | C | T | TCGA-05-4397-01A-01D-1265-08 | TCGA-05-4397-10A-01D-1265-08 | g.chr2:152423688C>T | c.13047G>A | c.(13045-13047)caG>caA | p.Q4349Q |
| LUAD | 2 | 152423858 | 152423858 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8299-01A-11D-2284-08 | TCGA-55-8299-10B-01D-2323-08 | g.chr2:152423858G>T | c.12877C>A | c.(12877-12879)Cac>Aac | p.H4293N |
| LUAD | 2 | 152423892 | 152423892 | + | Silent | SNP | C | C | T | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr2:152423892C>T | c.12843G>A | c.(12841-12843)caG>caA | p.Q4281Q |
| LUAD | 2 | 152425821 | 152425821 | + | Silent | SNP | G | G | A | TCGA-86-7701-01A-11D-2167-08 | TCGA-86-7701-10A-01D-2167-08 | g.chr2:152425821G>A | c.12393C>T | c.(12391-12393)tcC>tcT | p.S4131S |
| LUAD | 2 | 152426637 | 152426637 | + | Silent | SNP | G | G | A | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr2:152426637G>A | c.12285C>T | c.(12283-12285)aaC>aaT | p.N4095N |
| LUAD | 2 | 152426643 | 152426643 | + | Silent | SNP | G | G | A | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr2:152426643G>A | c.12279C>T | c.(12277-12279)gaC>gaT | p.D4093D |
| LUAD | 2 | 152426724 | 152426724 | + | Silent | SNP | G | G | T | TCGA-05-4244-01A-01D-1105-08 | TCGA-05-4244-10A-01D-1105-08 | g.chr2:152426724G>T | c.12198C>A | c.(12196-12198)atC>atA | p.I4066I |
| LUAD | 2 | 152426796 | 152426796 | + | Missense_Mutation | SNP | A | A | C | TCGA-17-Z051-01A-01W-0747-08 | TCGA-17-Z051-11A-01W-0747-08 | g.chr2:152426796A>C | c.12126T>G | c.(12124-12126)aaT>aaG | p.N4042K |
| LUAD | 2 | 152426863 | 152426863 | + | Missense_Mutation | SNP | A | A | T | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr2:152426863A>T | c.12059T>A | c.(12058-12060)gTg>gAg | p.V4020E |
| LUAD | 2 | 152426864 | 152426864 | + | Missense_Mutation | SNP | C | C | A | TCGA-62-8399-01A-21D-2323-08 | TCGA-62-8399-10A-01D-2323-08 | g.chr2:152426864C>A | c.12058G>T | c.(12058-12060)Gtg>Ttg | p.V4020L |
| LUAD | 2 | 152432208 | 152432208 | + | Splice_Site | SNP | C | C | T | TCGA-38-4631-01A-01D-1753-08 | TCGA-38-4631-11A-01D-1753-08 | g.chr2:152432208C>T | | c.e79+1 | |
| LUAD | 2 | 152432670 | 152432670 | + | Missense_Mutation | SNP | T | T | C | TCGA-91-6849-01A-11D-1945-08 | TCGA-91-6849-11A-01D-1945-08 | g.chr2:152432670T>C | c.11800A>G | c.(11800-11802)Agt>Ggt | p.S3934G |
| LUAD | 2 | 152432764 | 152432764 | + | Missense_Mutation | SNP | G | G | C | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr2:152432764G>C | c.11706C>G | c.(11704-11706)gaC>gaG | p.D3902E |
| LUAD | 2 | 152466325 | 152466325 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr2:152466325C>T | c.11599G>A | c.(11599-11601)Gat>Aat | p.D3867N |
| LUAD | 2 | 152466583 | 152466583 | + | Missense_Mutation | SNP | G | G | T | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr2:152466583G>T | c.11341C>A | c.(11341-11343)Cag>Aag | p.Q3781K |
| LUAD | 2 | 152466584 | 152466584 | + | Silent | SNP | G | G | T | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr2:152466584G>T | c.11340C>A | c.(11338-11340)gcC>gcA | p.A3780A |
| LUAD | 2 | 152467042 | 152467042 | + | Silent | SNP | G | G | A | TCGA-55-8299-01A-11D-2284-08 | TCGA-55-8299-10B-01D-2323-08 | g.chr2:152467042G>A | c.11277C>T | c.(11275-11277)gaC>gaT | p.D3759D |
| LUAD | 2 | 152467372 | 152467372 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-17-Z045-01A-01W-0746-08 | TCGA-17-Z045-11A-01W-0747-08 | g.chr2:152467372G>T | c.11085C>A | c.(11083-11085)taC>taA | p.Y3695* |
| LUAD | 2 | 152470789 | 152470789 | + | Splice_Site | SNP | C | C | A | TCGA-55-7570-01A-11D-2036-08 | TCGA-55-7570-10A-01D-2036-08 | g.chr2:152470789C>A | | c.e73+1 | |
| LUAD | 2 | 152470889 | 152470889 | + | Silent | SNP | T | T | A | TCGA-69-7979-01A-11D-2184-08 | TCGA-69-7979-10A-01D-2184-08 | g.chr2:152470889T>A | c.10773A>T | c.(10771-10773)gtA>gtT | p.V3591V |
| LUAD | 2 | 152470891 | 152470891 | + | Missense_Mutation | SNP | C | C | A | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr2:152470891C>A | c.10771G>T | c.(10771-10773)Gta>Tta | p.V3591L |
| LUAD | 2 | 152470916 | 152470916 | + | Silent | SNP | C | C | A | TCGA-75-7027-01A-11D-1945-08 | TCGA-75-7027-10A-01D-1946-08 | g.chr2:152470916C>A | c.10746G>T | c.(10744-10746)gtG>gtT | p.V3582V |
| LUAD | 2 | 152470990 | 152470990 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr2:152470990C>G | c.10672G>C | c.(10672-10674)Gac>Cac | p.D3558H |
| LUAD | 2 | 152472515 | 152472515 | + | Splice_Site | SNP | C | C | G | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr2:152472515C>G | | c.e72+1 | |
| LUAD | 2 | 152472566 | 152472566 | + | Missense_Mutation | SNP | C | C | G | TCGA-50-5941-01A-11D-1753-08 | TCGA-50-5941-10A-01D-1753-08 | g.chr2:152472566C>G | c.10510G>C | c.(10510-10512)Gat>Cat | p.D3504H |
| LUAD | 2 | 152472617 | 152472617 | + | Missense_Mutation | SNP | A | A | T | TCGA-55-7227-01A-11D-2036-08 | TCGA-55-7227-10A-01D-2036-08 | g.chr2:152472617A>T | c.10459T>A | c.(10459-10461)Tat>Aat | p.Y3487N |
| LUAD | 2 | 152474831 | 152474831 | + | Silent | SNP | C | C | A | TCGA-MP-A4TC-01A-11D-A24P-08 | TCGA-MP-A4TC-10A-01D-A24P-08 | g.chr2:152474831C>A | c.10305G>T | c.(10303-10305)ccG>ccT | p.P3435P |
| LUAD | 2 | 152476160 | 152476160 | + | Silent | SNP | A | A | G | TCGA-55-8614-01A-11D-2393-08 | TCGA-55-8614-10A-01D-2393-08 | g.chr2:152476160A>G | c.9948T>C | c.(9946-9948)cgT>cgC | p.R3316R |
| LUAD | 2 | 152476249 | 152476249 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-8203-01A-11D-2238-08 | TCGA-55-8203-10A-01D-2238-08 | g.chr2:152476249G>C | c.9859C>G | c.(9859-9861)Cag>Gag | p.Q3287E |
| LUAD | 2 | 152482118 | 152482118 | + | Missense_Mutation | SNP | G | G | A | TCGA-L4-A4E5-01A-11D-A24P-08 | TCGA-L4-A4E5-10A-01D-A24P-08 | g.chr2:152482118G>A | c.9653C>T | c.(9652-9654)aCc>aTc | p.T3218I |
| LUAD | 2 | 152483651 | 152483651 | + | Silent | SNP | C | C | T | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr2:152483651C>T | c.9483G>A | c.(9481-9483)gtG>gtA | p.V3161V |
| LUAD | 2 | 152483676 | 152483676 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5946-01A-11D-1753-08 | TCGA-50-5946-10A-01D-1753-08 | g.chr2:152483676C>A | c.9458G>T | c.(9457-9459)tGg>tTg | p.W3153L |
| LUAD | 2 | 152484098 | 152484098 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr2:152484098G>A | c.9353C>T | c.(9352-9354)aCg>aTg | p.T3118M |
| LUAD | 2 | 152484188 | 152484188 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8510-01A-11D-2393-08 | TCGA-55-8510-10A-01D-2393-08 | g.chr2:152484188C>A | c.9263G>T | c.(9262-9264)aGc>aTc | p.S3088I |
| LUAD | 2 | 152484282 | 152484282 | + | Missense_Mutation | SNP | C | C | T | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr2:152484282C>T | c.9169G>A | c.(9169-9171)Gac>Aac | p.D3057N |
| LUAD | 2 | 152484310 | 152484310 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z022-01A-01W-0746-08 | TCGA-17-Z022-11A-01W-0746-08 | g.chr2:152484310G>T | c.9141C>A | c.(9139-9141)caC>caA | p.H3047Q |
| LUAD | 2 | 152487259 | 152487259 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-7980-01A-11D-2184-08 | TCGA-69-7980-10A-01D-2184-08 | g.chr2:152487259C>A | c.8964G>T | c.(8962-8964)ttG>ttT | p.L2988F |
| LUAD | 2 | 152487674 | 152487674 | + | Intron | SNP | C | C | A | TCGA-44-6774-01A-21D-1855-08 | TCGA-44-6774-10A-01D-1855-08 | g.chr2:152487674C>A | | | |
| LUAD | 2 | 152490372 | 152490372 | + | Intron | SNP | C | C | T | TCGA-86-8056-01A-11D-2238-08 | TCGA-86-8056-10A-01D-2238-08 | g.chr2:152490372C>T | | | |
| LUAD | 2 | 152492776 | 152492776 | + | Intron | SNP | C | C | A | TCGA-MN-A4N1-01A-11D-A24P-08 | TCGA-MN-A4N1-10A-01D-A24P-08 | g.chr2:152492776C>A | | | |
| LUAD | 2 | 152492824 | 152492824 | + | Intron | SNP | C | C | A | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr2:152492824C>A | | | |
| LUAD | 2 | 152496381 | 152496382 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-17-Z015-01A-01W-0746-08 | TCGA-17-Z015-11A-01W-0746-08 | g.chr2:152496381_152496382insA | c.8878_8879insT | c.(8878-8880)actfs | p.T2960fs |
| LUAD | 2 | 152497098 | 152497098 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr2:152497098C>G | c.8456G>C | c.(8455-8457)tGg>tCg | p.W2819S |
| LUAD | 2 | 152499151 | 152499151 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-91-6836-01A-21D-1855-08 | TCGA-91-6836-11A-01D-1855-08 | g.chr2:152499151A>C | c.8310T>G | c.(8308-8310)taT>taG | p.Y2770* |
| LUAD | 2 | 152499796 | 152499796 | + | Silent | SNP | C | C | T | TCGA-95-8039-01A-11D-2238-08 | TCGA-95-8039-10A-01D-2238-08 | g.chr2:152499796C>T | c.8028G>A | c.(8026-8028)gaG>gaA | p.E2676E |
| LUAD | 2 | 152500419 | 152500419 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr2:152500419G>T | c.7869C>A | c.(7867-7869)gaC>gaA | p.D2623E |
| LUAD | 2 | 152500536 | 152500536 | + | Silent | SNP | C | C | T | TCGA-78-7539-01A-11D-2063-08 | TCGA-78-7539-10A-01D-2063-08 | g.chr2:152500536C>T | c.7752G>A | c.(7750-7752)caG>caA | p.Q2584Q |
| LUAD | 2 | 152500637 | 152500637 | + | Missense_Mutation | SNP | A | A | G | TCGA-73-4658-01A-01D-1753-08 | TCGA-73-4658-11A-01D-1753-08 | g.chr2:152500637A>G | c.7651T>C | c.(7651-7653)Tac>Cac | p.Y2551H |
| LUAD | 2 | 152506707 | 152506707 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-6969-01A-11D-1945-08 | TCGA-55-6969-11A-01D-1945-08 | g.chr2:152506707C>G | c.7414G>C | c.(7414-7416)Gcc>Ccc | p.A2472P |
| LUAD | 2 | 152506830 | 152506830 | + | Missense_Mutation | SNP | C | C | G | TCGA-69-7980-01A-11D-2184-08 | TCGA-69-7980-10A-01D-2184-08 | g.chr2:152506830C>G | c.7291G>C | c.(7291-7293)Gag>Cag | p.E2431Q |
| LUAD | 2 | 152507090 | 152507090 | + | Missense_Mutation | SNP | C | C | G | TCGA-69-7765-01A-11D-2167-08 | TCGA-69-7765-10A-01D-2167-08 | g.chr2:152507090C>G | c.7225G>C | c.(7225-7227)Gag>Cag | p.E2409Q |
| LUAD | 2 | 152507102 | 152507102 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-17-Z022-01A-01W-0746-08 | TCGA-17-Z022-11A-01W-0746-08 | g.chr2:152507102C>A | c.7213G>T | c.(7213-7215)Gaa>Taa | p.E2405* |
| LUAD | 2 | 152507197 | 152507197 | + | Missense_Mutation | SNP | T | T | A | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr2:152507197T>A | c.7118A>T | c.(7117-7119)cAg>cTg | p.Q2373L |
| LUAD | 2 | 152507201 | 152507201 | + | Missense_Mutation | SNP | A | A | T | TCGA-78-7166-01A-12D-2063-08 | TCGA-78-7166-11A-01D-2063-08 | g.chr2:152507201A>T | c.7114T>A | c.(7114-7116)Tgt>Agt | p.C2372S |
| LUAD | 2 | 152507221 | 152507221 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8616-01A-11D-2393-08 | TCGA-55-8616-10A-01D-2393-08 | g.chr2:152507221C>A | c.7094G>T | c.(7093-7095)gGa>gTa | p.G2365V |
| LUAD | 2 | 152507232 | 152507232 | + | Silent | SNP | C | C | A | TCGA-NJ-A4YF-01A-12D-A25L-08 | TCGA-NJ-A4YF-10A-01D-A25L-08 | g.chr2:152507232C>A | c.7083G>T | c.(7081-7083)gtG>gtT | p.V2361V |
| LUAD | 2 | 152507313 | 152507313 | + | Silent | SNP | G | G | T | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr2:152507313G>T | c.7002C>A | c.(7000-7002)tcC>tcA | p.S2334S |
| LUAD | 2 | 152512820 | 152512820 | + | Silent | SNP | G | G | A | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr2:152512820G>A | c.6342C>T | c.(6340-6342)caC>caT | p.H2114H |
| LUAD | 2 | 152512848 | 152512870 | + | Frame_Shift_Del | DEL | TTTTTCTTGTACTCCCGATCAGA | TTTTTCTTGTACTCCCGATCAGA | - | TCGA-78-7158-01A-11D-2036-08 | TCGA-78-7158-10A-01D-2036-08 | g.chr2:152512848_152512870delTTTTTCTTGTACTCCCGATCAGA | c.6292_6314delTCTGATCGGGAGTACAAGAAAAA | c.(6292-6315)tctgatcgggagtacaagaaaaacfs | p.SDREYKKN2098fs |
| LUAD | 2 | 152514544 | 152514544 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-6969-01A-11D-1945-08 | TCGA-55-6969-11A-01D-1945-08 | g.chr2:152514544C>G | c.6136G>C | c.(6136-6138)Gca>Cca | p.A2046P |
| LUAD | 2 | 152518729 | 152518729 | + | Missense_Mutation | SNP | G | G | T | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr2:152518729G>T | c.5890C>A | c.(5890-5892)Cca>Aca | p.P1964T |
| LUAD | 2 | 152518738 | 152518738 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr2:152518738G>T | c.5881C>A | c.(5881-5883)Cgc>Agc | p.R1961S |
| LUAD | 2 | 152521350 | 152521350 | + | Missense_Mutation | SNP | C | C | A | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr2:152521350C>A | c.5266G>T | c.(5266-5268)Gac>Tac | p.D1756Y |
| LUAD | 2 | 152521350 | 152521350 | + | Missense_Mutation | SNP | C | C | A | TCGA-MP-A4TC-01A-11D-A24P-08 | TCGA-MP-A4TC-10A-01D-A24P-08 | g.chr2:152521350C>A | c.5266G>T | c.(5266-5268)Gac>Tac | p.D1756Y |
| LUAD | 2 | 152521351 | 152521351 | + | Missense_Mutation | SNP | C | C | A | TCGA-MP-A4TC-01A-11D-A24P-08 | TCGA-MP-A4TC-10A-01D-A24P-08 | g.chr2:152521351C>A | c.5265G>T | c.(5263-5265)aaG>aaT | p.K1755N |
| LUAD | 2 | 152521927 | 152521927 | + | Missense_Mutation | SNP | G | G | T | TCGA-91-6831-01A-11D-1855-08 | TCGA-91-6831-11A-02D-1855-08 | g.chr2:152521927G>T | c.5158C>A | c.(5158-5160)Ccc>Acc | p.P1720T |
| LUAD | 2 | 152522011 | 152522011 | + | Missense_Mutation | SNP | C | C | T | TCGA-17-Z015-01A-01W-0746-08 | TCGA-17-Z015-11A-01W-0746-08 | g.chr2:152522011C>T | c.5074G>A | c.(5074-5076)Ggc>Agc | p.G1692S |
| LUAD | 2 | 152522015 | 152522015 | + | Silent | SNP | C | C | A | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr2:152522015C>A | c.5070G>T | c.(5068-5070)ggG>ggT | p.G1690G |
| LUAD | 2 | 152522052 | 152522052 | + | Splice_Site | SNP | T | T | A | TCGA-05-4249-01A-01D-1105-08 | TCGA-05-4249-10A-01D-1105-08 | g.chr2:152522052T>A | c.5033A>T | c.(5032-5034)aAt>aTt | p.N1678I |
| LUAD | 2 | 152522680 | 152522680 | + | Missense_Mutation | SNP | G | G | A | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr2:152522680G>A | c.4955C>T | c.(4954-4956)tCa>tTa | p.S1652L |
| LUAD | 2 | 152522697 | 152522697 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr2:152522697G>T | c.4938C>A | c.(4936-4938)aaC>aaA | p.N1646K |
| LUAD | 2 | 152527651 | 152527651 | + | Silent | SNP | G | G | A | TCGA-49-4505-01A-01D-1931-08 | TCGA-49-4505-11A-01D-1265-08 | g.chr2:152527651G>A | c.4392C>T | c.(4390-4392)ggC>ggT | p.G1464G |
| LUAD | 2 | 152527689 | 152527689 | + | Missense_Mutation | SNP | T | T | C | TCGA-05-4430-01A-02D-1265-08 | TCGA-05-4430-10A-01D-1265-08 | g.chr2:152527689T>C | c.4354A>G | c.(4354-4356)Att>Gtt | p.I1452V |
| LUAD | 2 | 152529000 | 152529000 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr2:152529000C>A | c.4182G>T | c.(4180-4182)aaG>aaT | p.K1394N |
| LUAD | 2 | 152529152 | 152529152 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-8281-01A-11D-2284-08 | TCGA-86-8281-10A-01D-2284-08 | g.chr2:152529152C>G | c.4030G>C | c.(4030-4032)Gtg>Ctg | p.V1344L |
| LUAD | 2 | 152531009 | 152531009 | + | Silent | SNP | C | C | G | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr2:152531009C>G | c.3969G>C | c.(3967-3969)tcG>tcC | p.S1323S |
| LUAD | 2 | 152534389 | 152534389 | + | Splice_Site | SNP | C | C | A | TCGA-55-A48X-01A-11D-A24D-08 | TCGA-55-A48X-10A-01D-A24F-08 | g.chr2:152534389C>A | | c.e33+1 | |
| LUAD | 2 | 152534533 | 152534533 | + | Missense_Mutation | SNP | C | C | A | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr2:152534533C>A | c.3424G>T | c.(3424-3426)Gat>Tat | p.D1142Y |
| LUAD | 2 | 152534572 | 152534573 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr2:152534572_152534573insT | c.3384_3385insA | c.(3382-3387)aaagacfs | p.D1129fs |
| LUAD | 2 | 152534675 | 152534675 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4398-01A-01D-1265-08 | TCGA-05-4398-10A-01D-1265-08 | g.chr2:152534675C>A | c.3282G>T | c.(3280-3282)aaG>aaT | p.K1094N |
| LUAD | 2 | 152536264 | 152536264 | + | Missense_Mutation | SNP | C | C | A | TCGA-91-A4BC-01A-11D-A24D-08 | TCGA-91-A4BC-10A-01D-A24F-08 | g.chr2:152536264C>A | c.3226G>T | c.(3226-3228)Gcc>Tcc | p.A1076S |
| LUAD | 2 | 152537297 | 152537297 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8089-01A-11D-2238-08 | TCGA-55-8089-10A-01D-2238-08 | g.chr2:152537297C>T | c.2989G>A | c.(2989-2991)Gaa>Aaa | p.E997K |
| LUAD | 2 | 152539283 | 152539283 | + | Splice_Site | SNP | C | C | A | TCGA-17-Z060-01A-01W-0747-08 | TCGA-17-Z060-11A-01W-0747-08 | g.chr2:152539283C>A | c.2836G>T | c.(2836-2838)Gtt>Ttt | p.V946F |
| LUAD | 2 | 152541305 | 152541305 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z015-01A-01W-0746-08 | TCGA-17-Z015-11A-01W-0746-08 | g.chr2:152541305G>A | c.2822C>T | c.(2821-2823)gCg>gTg | p.A941V |
| LUAD | 2 | 152543993 | 152543993 | + | Silent | SNP | G | G | A | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr2:152543993G>A | c.2577C>T | c.(2575-2577)ctC>ctT | p.L859L |
| LUAD | 2 | 152544162 | 152544162 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr2:152544162G>A | c.2501C>T | c.(2500-2502)gCc>gTc | p.A834V |
| LUAD | 2 | 152544853 | 152544853 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-A492-01A-11D-A24D-08 | TCGA-55-A492-10A-01D-A24F-08 | g.chr2:152544853C>A | c.2368G>T | c.(2368-2370)Gct>Tct | p.A790S |
| LUAD | 2 | 152544853 | 152544853 | + | Missense_Mutation | SNP | C | C | A | TCGA-62-8399-01A-21D-2323-08 | TCGA-62-8399-10A-01D-2323-08 | g.chr2:152544853C>A | c.2368G>T | c.(2368-2370)Gct>Tct | p.A790S |
| LUAD | 2 | 152544855 | 152544855 | + | Missense_Mutation | SNP | T | T | A | TCGA-44-A4SU-01A-11D-A24P-08 | TCGA-44-A4SU-10A-01D-A24P-08 | g.chr2:152544855T>A | c.2366A>T | c.(2365-2367)gAt>gTt | p.D789V |
| LUAD | 2 | 152544861 | 152544861 | + | Missense_Mutation | SNP | G | G | T | TCGA-NJ-A4YI-01A-11D-A25L-08 | TCGA-NJ-A4YI-10A-01D-A25L-08 | g.chr2:152544861G>T | c.2360C>A | c.(2359-2361)cCa>cAa | p.P787Q |
| LUAD | 2 | 152548389 | 152548389 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-MP-A4T4-01A-11D-A25L-08 | TCGA-MP-A4T4-10A-01D-A25L-08 | g.chr2:152548389G>A | c.2200C>T | c.(2200-2202)Cag>Tag | p.Q734* |
| LUAD | 2 | 152548676 | 152548676 | + | Missense_Mutation | SNP | C | C | G | TCGA-78-7161-01A-11D-2036-08 | TCGA-78-7161-10A-01D-2036-08 | g.chr2:152548676C>G | c.2003G>C | c.(2002-2004)aGa>aCa | p.R668T |
| LUAD | 2 | 152551035 | 152551035 | + | Splice_Site | SNP | C | C | G | TCGA-44-6145-01A-11D-1753-08 | TCGA-44-6145-10A-01D-1753-08 | g.chr2:152551035C>G | | c.e19+1 | |
| LUAD | 2 | 152552143 | 152552143 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-97-7547-01A-11D-2036-08 | TCGA-97-7547-10A-01D-2036-08 | g.chr2:152552143delA | c.1623delT | c.(1621-1623)cctfs | p.P541fs |
| LUAD | 2 | 152553214 | 152553214 | + | Silent | SNP | G | G | A | TCGA-17-Z056-01A-01W-0747-08 | TCGA-17-Z056-11A-01W-0747-08 | g.chr2:152553214G>A | c.1506C>T | c.(1504-1506)ttC>ttT | p.F502F |
| LUAD | 2 | 152553228 | 152553228 | + | Missense_Mutation | SNP | C | C | G | TCGA-J2-A4AD-01A-11D-A24D-08 | TCGA-J2-A4AD-10A-01D-A24F-08 | g.chr2:152553228C>G | c.1492G>C | c.(1492-1494)Gat>Cat | p.D498H |
| LUAD | 2 | 152553887 | 152553887 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr2:152553887T>A | c.1342A>T | c.(1342-1344)Aaa>Taa | p.K448* |
| LUAD | 2 | 152553915 | 152553915 | + | Silent | SNP | G | G | A | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr2:152553915G>A | c.1314C>T | c.(1312-1314)ttC>ttT | p.F438F |
| LUAD | 2 | 152553948 | 152553948 | + | Silent | SNP | T | T | C | TCGA-86-8358-01A-11D-2323-08 | TCGA-86-8358-10A-01D-2323-08 | g.chr2:152553948T>C | c.1281A>G | c.(1279-1281)ttA>ttG | p.L427L |
| LUAD | 2 | 152553972 | 152553972 | + | Splice_Site | SNP | C | C | T | TCGA-44-A4SS-01A-11D-A24P-08 | TCGA-44-A4SS-10A-01D-A24P-08 | g.chr2:152553972C>T | | c.e15-1 | |
| LUAD | 2 | 152554106 | 152554106 | + | Silent | SNP | C | C | T | TCGA-91-6836-01A-21D-1855-08 | TCGA-91-6836-11A-01D-1855-08 | g.chr2:152554106C>T | c.1209G>A | c.(1207-1209)gaG>gaA | p.E403E |
| LUAD | 2 | 152554122 | 152554122 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z030-01A-01W-0746-08 | TCGA-17-Z030-11A-01W-0746-08 | g.chr2:152554122C>A | c.1193G>T | c.(1192-1194)aGc>aTc | p.S398I |
| LUAD | 2 | 152566225 | 152566225 | + | Missense_Mutation | SNP | T | T | A | TCGA-64-1676-01A-01D-0969-08 | TCGA-64-1676-10A-01D-0969-08 | g.chr2:152566225T>A | c.980A>T | c.(979-981)cAg>cTg | p.Q327L |
| LUAD | 2 | 152579940 | 152579940 | + | Missense_Mutation | SNP | G | G | C | TCGA-69-A59K-01A-11D-A25L-08 | TCGA-69-A59K-10A-01D-A25L-08 | g.chr2:152579940G>C | c.673C>G | c.(673-675)Ccg>Gcg | p.P225A |
| LUAD | 2 | 152581406 | 152581406 | + | Missense_Mutation | SNP | C | C | T | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr2:152581406C>T | c.472G>A | c.(472-474)Gaa>Aaa | p.E158K |
| LUAD | 2 | 152582033 | 152582033 | + | Silent | SNP | T | T | C | TCGA-78-7161-01A-11D-2036-08 | TCGA-78-7161-10A-01D-2036-08 | g.chr2:152582033T>C | c.336A>G | c.(334-336)ccA>ccG | p.P112P |
| LUSC | 2 | 152348670 | 152348670 | + | Silent | SNP | C | C | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr2:152348670C>T | c.19431G>A | c.(19429-19431)caG>caA | p.Q6477Q |
| LUSC | 2 | 152373009 | 152373009 | + | Silent | SNP | G | G | A | TCGA-66-2793-01A-01D-1267-08 | TCGA-66-2793-11A-01D-1267-08 | g.chr2:152373009G>A | c.17766C>T | c.(17764-17766)taC>taT | p.Y5922Y |
| LUSC | 2 | 152374923 | 152374923 | + | Missense_Mutation | SNP | T | T | C | TCGA-46-3769-01A-01D-0983-08 | TCGA-46-3769-10A-01D-0983-08 | g.chr2:152374923T>C | c.17606A>G | c.(17605-17607)aAg>aGg | p.K5869R |
| LUSC | 2 | 152382499 | 152382499 | + | Silent | SNP | G | G | C | TCGA-66-2783-01A-01D-1267-08 | TCGA-66-2783-11A-01D-1267-08 | g.chr2:152382499G>C | c.17031C>G | c.(17029-17031)gtC>gtG | p.V5677V |
| LUSC | 2 | 152385743 | 152385743 | + | Missense_Mutation | SNP | G | G | T | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr2:152385743G>T | c.16613C>A | c.(16612-16614)gCc>gAc | p.A5538D |
| LUSC | 2 | 152402505 | 152402505 | + | Missense_Mutation | SNP | T | T | A | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr2:152402505T>A | c.15371A>T | c.(15370-15372)tAc>tTc | p.Y5124F |
| LUSC | 2 | 152404000 | 152404000 | + | Silent | SNP | A | A | C | TCGA-33-4566-01A-01D-1441-08 | TCGA-33-4566-11A-01D-1441-08 | g.chr2:152404000A>C | c.15207T>G | c.(15205-15207)tcT>tcG | p.S5069S |
| LUSC | 2 | 152410492 | 152410492 | + | Silent | SNP | G | G | A | TCGA-39-5030-01A-01D-1441-08 | TCGA-39-5030-11A-01D-1441-08 | g.chr2:152410492G>A | c.14373C>T | c.(14371-14373)atC>atT | p.I4791I |
| LUSC | 2 | 152410492 | 152410492 | + | Silent | SNP | G | G | A | TCGA-66-2778-01A-02D-1522-08 | TCGA-66-2778-11A-01D-1522-08 | g.chr2:152410492G>A | c.14373C>T | c.(14371-14373)atC>atT | p.I4791I |
| LUSC | 2 | 152420154 | 152420154 | + | Missense_Mutation | SNP | A | A | G | TCGA-63-5128-01A-01D-1441-08 | TCGA-63-5128-10A-01D-1441-08 | g.chr2:152420154A>G | c.13556T>C | c.(13555-13557)gTt>gCt | p.V4519A |
| LUSC | 2 | 152422331 | 152422331 | + | Missense_Mutation | SNP | C | C | T | TCGA-60-2726-01A-01D-1522-08 | TCGA-60-2726-11A-01D-1522-08 | g.chr2:152422331C>T | c.13057G>A | c.(13057-13059)Gtc>Atc | p.V4353I |
| LUSC | 2 | 152427027 | 152427027 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2786-01A-01D-1522-08 | TCGA-66-2786-11A-01D-1522-08 | g.chr2:152427027C>A | c.11999G>T | c.(11998-12000)aGg>aTg | p.R4000M |
| LUSC | 2 | 152427061 | 152427061 | + | Missense_Mutation | SNP | C | C | T | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr2:152427061C>T | c.11965G>A | c.(11965-11967)Gat>Aat | p.D3989N |
| LUSC | 2 | 152427088 | 152427088 | + | Missense_Mutation | SNP | T | T | C | TCGA-18-3414-01A-01D-0983-08 | TCGA-18-3414-11A-01D-0983-08 | g.chr2:152427088T>C | c.11938A>G | c.(11938-11940)Atg>Gtg | p.M3980V |
| LUSC | 2 | 152470912 | 152470913 | + | Missense_Mutation | DNP | CC | CC | AA | TCGA-22-5472-01A-01D-1632-08 | TCGA-22-5472-11A-11D-1632-08 | g.chr2:152470912_152470913CC>AA | c.10749_10750GG>TT | c.(10747-10752)ctGGcc>ctTTcc | p.A3584S |
| LUSC | 2 | 152473910 | 152473910 | + | Missense_Mutation | SNP | A | A | C | TCGA-22-5491-01A-01D-1632-08 | TCGA-22-5491-11A-01D-1632-08 | g.chr2:152473910A>C | c.10420T>G | c.(10420-10422)Tta>Gta | p.L3474V |
| LUSC | 2 | 152483674 | 152483674 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2768-01A-01D-1522-08 | TCGA-66-2768-11A-01D-1522-08 | g.chr2:152483674C>A | c.9460G>T | c.(9460-9462)Gtc>Ttc | p.V3154F |
| LUSC | 2 | 152487332 | 152487332 | + | Splice_Site | SNP | C | C | T | TCGA-18-5592-01A-01D-1632-08 | TCGA-18-5592-11A-11D-1632-08 | g.chr2:152487332C>T | c.8891G>A | c.(8890-8892)cGt>cAt | p.R2964H |
| LUSC | 2 | 152496966 | 152496966 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr2:152496966C>G | c.8588G>C | c.(8587-8589)aGc>aCc | p.S2863T |
| LUSC | 2 | 152497110 | 152497110 | + | Missense_Mutation | SNP | G | G | C | TCGA-56-6545-01A-11D-1817-08 | TCGA-56-6545-10A-01D-1817-08 | g.chr2:152497110G>C | c.8444C>G | c.(8443-8445)cCc>cGc | p.P2815R |
| LUSC | 2 | 152500339 | 152500339 | + | Missense_Mutation | SNP | T | T | A | TCGA-22-4604-01A-01D-1267-08 | TCGA-22-4604-11A-01D-1267-08 | g.chr2:152500339T>A | c.7949A>T | c.(7948-7950)cAg>cTg | p.Q2650L |
| LUSC | 2 | 152501057 | 152501057 | + | Missense_Mutation | SNP | C | C | A | TCGA-21-5784-01A-01D-1632-08 | TCGA-21-5784-10A-01D-1632-08 | g.chr2:152501057C>A | c.7569G>T | c.(7567-7569)aaG>aaT | p.K2523N |
| LUSC | 2 | 152512352 | 152512352 | + | Silent | SNP | C | C | T | TCGA-21-1077-01A-01D-1521-08 | TCGA-21-1077-11A-01D-1521-08 | g.chr2:152512352C>T | c.6681G>A | c.(6679-6681)caG>caA | p.Q2227Q |
| LUSC | 2 | 152512796 | 152512796 | + | Silent | SNP | G | G | C | TCGA-18-3416-01A-01D-0983-08 | TCGA-18-3416-11A-01D-0983-08 | g.chr2:152512796G>C | c.6366C>G | c.(6364-6366)gtC>gtG | p.V2122V |
| LUSC | 2 | 152520196 | 152520196 | + | Missense_Mutation | SNP | T | T | A | TCGA-18-3417-01A-01D-1441-08 | TCGA-18-3417-11A-01D-1441-08 | g.chr2:152520196T>A | c.5629A>T | c.(5629-5631)Agt>Tgt | p.S1877C |
| LUSC | 2 | 152520222 | 152520222 | + | Missense_Mutation | SNP | G | G | A | TCGA-21-5787-01A-01D-1632-08 | TCGA-21-5787-10A-01D-1632-08 | g.chr2:152520222G>A | c.5603C>T | c.(5602-5604)tCc>tTc | p.S1868F |
| LUSC | 2 | 152520262 | 152520262 | + | Missense_Mutation | SNP | C | C | A | TCGA-34-5239-01A-21D-1817-08 | TCGA-34-5239-10A-01D-1817-08 | g.chr2:152520262C>A | c.5563G>T | c.(5563-5565)Gac>Tac | p.D1855Y |
| LUSC | 2 | 152521924 | 152521924 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr2:152521924C>A | c.5161G>T | c.(5161-5163)Gag>Tag | p.E1721* |
| LUSC | 2 | 152522777 | 152522777 | + | Missense_Mutation | SNP | C | C | A | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr2:152522777C>A | c.4858G>T | c.(4858-4860)Gcc>Tcc | p.A1620S |
| LUSC | 2 | 152522861 | 152522861 | + | Missense_Mutation | SNP | T | T | G | TCGA-39-5029-01A-01D-1441-08 | TCGA-39-5029-11A-01D-1441-08 | g.chr2:152522861T>G | c.4774A>C | c.(4774-4776)Agt>Cgt | p.S1592R |
| LUSC | 2 | 152525607 | 152525607 | + | Silent | SNP | C | C | T | TCGA-22-5482-01A-01D-1632-08 | TCGA-22-5482-11A-01D-1632-08 | g.chr2:152525607C>T | c.4545G>A | c.(4543-4545)aaG>aaA | p.K1515K |
| LUSC | 2 | 152527701 | 152527701 | + | Missense_Mutation | SNP | C | C | T | TCGA-21-1077-01A-01D-1521-08 | TCGA-21-1077-11A-01D-1521-08 | g.chr2:152527701C>T | c.4342G>A | c.(4342-4344)Gga>Aga | p.G1448R |
| LUSC | 2 | 152529031 | 152529031 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-66-2757-01A-01D-1522-08 | TCGA-66-2757-11A-01D-1522-08 | g.chr2:152529031delG | c.4151delC | c.(4150-4152)cctfs | p.P1384fs |
| LUSC | 2 | 152529046 | 152529046 | + | Missense_Mutation | SNP | G | G | T | TCGA-56-5897-01A-11D-1632-08 | TCGA-56-5897-10A-01D-1632-08 | g.chr2:152529046G>T | c.4136C>A | c.(4135-4137)aCc>aAc | p.T1379N |
| LUSC | 2 | 152529183 | 152529183 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2767-01A-01D-1522-08 | TCGA-66-2767-11A-01D-1522-08 | g.chr2:152529183C>A | c.3999G>T | c.(3997-3999)aaG>aaT | p.K1333N |
| LUSC | 2 | 152543961 | 152543961 | + | Missense_Mutation | SNP | G | G | A | TCGA-85-6561-01A-11D-1817-08 | TCGA-85-6561-10A-01D-1817-08 | g.chr2:152543961G>A | c.2609C>T | c.(2608-2610)tCc>tTc | p.S870F |
| LUSC | 2 | 152544034 | 152544035 | + | Nonsense_Mutation | DNP | TC | TC | AT | TCGA-34-5928-01A-11D-1817-08 | TCGA-34-5928-10A-01D-1817-08 | g.chr2:152544034_152544035TC>AT | c.2535_2536GA>AT | c.(2533-2538)aaGAaa>aaATaa | p.K846* |
| LUSC | 2 | 152553725 | 152553725 | + | Silent | SNP | G | G | A | TCGA-34-2600-01A-01D-1522-08 | TCGA-34-2600-11A-01D-1522-08 | g.chr2:152553725G>A | c.1407C>T | c.(1405-1407)ggC>ggT | p.G469G |
| LUSC | 2 | 152580773 | 152580773 | + | Splice_Site | SNP | C | C | A | TCGA-66-2795-01A-02D-0983-08 | TCGA-66-2795-11A-01D-0983-08 | g.chr2:152580773C>A | | c.e8+1 | |
| LUSC | 2 | 152582017 | 152582017 | + | Missense_Mutation | SNP | C | C | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr2:152582017C>T | c.352G>A | c.(352-354)Gat>Aat | p.D118N |
| OV | 2 | 152346909 | 152346909 | + | Missense_Mutation | SNP | C | C | T | TCGA-13-0887-01A-01W-0421-09 | TCGA-13-0887-10A-01W-0421-09 | g.chr2:152346909C>T | c.19706G>A | c.(19705-19707)gGg>gAg | p.G6569E |
| OV | 2 | 152362072 | 152362072 | + | Missense_Mutation | SNP | C | C | G | TCGA-13-0923-01A-01W-0420-08 | TCGA-13-0923-10A-01D-0399-08 | g.chr2:152362072C>G | c.18559G>C | c.(18559-18561)Gaa>Caa | p.E6187Q |
| OV | 2 | 152393705 | 152393705 | + | Missense_Mutation | SNP | A | A | C | TCGA-13-1492-01A-01D-0472-08 | TCGA-13-1492-10A-01W-0545-08 | g.chr2:152393705A>C | c.16045T>G | c.(16045-16047)Tat>Gat | p.Y5349D |
| OV | 2 | 152397960 | 152397960 | + | Splice_Site | DEL | C | C | - | TCGA-23-1122-01A-01W-0486-08 | TCGA-23-1122-10A-01W-0486-08 | g.chr2:152397960delC | | c.e108+1 | |
| OV | 2 | 152409234 | 152409234 | + | Silent | SNP | A | A | G | TCGA-24-1464-01A-01W-0549-09 | TCGA-24-1464-10A-01W-0549-09 | g.chr2:152409234A>G | c.14685T>C | c.(14683-14685)gaT>gaC | p.D4895D |
| OV | 2 | 152423804 | 152423804 | + | Missense_Mutation | SNP | C | C | T | TCGA-24-1843-01A-01W-0639-09 | TCGA-24-1843-10A-01W-0639-09 | g.chr2:152423804C>T | c.12931G>A | c.(12931-12933)Gcc>Acc | p.A4311T |
| OV | 2 | 152427044 | 152427044 | + | Missense_Mutation | SNP | C | C | A | TCGA-29-1766-01A-01W-0633-09 | TCGA-29-1766-10A-01W-0634-09 | g.chr2:152427044C>A | c.11982G>T | c.(11980-11982)caG>caT | p.Q3994H |
| OV | 2 | 152499124 | 152499124 | + | Silent | SNP | G | G | T | TCGA-25-1326-01A-01W-0492-08 | TCGA-25-1326-10A-01W-0492-08 | g.chr2:152499124G>T | c.8337C>A | c.(8335-8337)atC>atA | p.I2779I |
| OV | 2 | 152500388 | 152500388 | + | Silent | SNP | G | G | A | TCGA-23-1809-01A-01W-0633-09 | TCGA-23-1809-10A-01W-0634-09 | g.chr2:152500388G>A | c.7900C>T | c.(7900-7902)Ctg>Ttg | p.L2634L |
| OV | 2 | 152512413 | 152512413 | + | Missense_Mutation | SNP | T | T | G | TCGA-13-1499-01A-01W-0549-09 | TCGA-13-1499-10A-01W-0549-09 | g.chr2:152512413T>G | c.6620A>C | c.(6619-6621)cAc>cCc | p.H2207P |
| OV | 2 | 152553150 | 152553150 | + | Splice_Site | SNP | C | C | T | TCGA-29-1775-01A-01W-0639-09 | TCGA-29-1775-10A-01W-0639-09 | g.chr2:152553150C>T | | c.e17+1 | |
| OV | 2 | 152566216 | 152566217 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-04-1331-01A-01W-0486-08 | TCGA-04-1331-10A-01W-0486-08 | g.chr2:152566216_152566217insT | c.988_989insA | c.(988-990)acafs | p.T330fs |
| PAAD | 2 | 152346952 | 152346952 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152346952G>A | c.19663C>T | c.(19663-19665)Cat>Tat | p.H6555Y |
| PAAD | 2 | 152352790 | 152352790 | + | Splice_Site | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152352790C>T | c.18918G>A | c.(18916-18918)tcG>tcA | p.S6306S |
| PAAD | 2 | 152364595 | 152364595 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152364595G>A | c.18272C>T | c.(18271-18273)tCc>tTc | p.S6091F |
| PAAD | 2 | 152376273 | 152376273 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FB-AAQ0-01A-31D-A40W-08 | TCGA-FB-AAQ0-11A-11D-A40W-08 | g.chr2:152376273G>A | c.17386C>T | c.(17386-17388)Cga>Tga | p.R5796* |
| PAAD | 2 | 152381050 | 152381050 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152381050C>A | c.17250G>T | c.(17248-17250)caG>caT | p.Q5750H |
| PAAD | 2 | 152419185 | 152419185 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152419185C>T | c.13728G>A | c.(13726-13728)acG>acA | p.T4576T |
| PAAD | 2 | 152420121 | 152420121 | + | Splice_Site | SNP | G | G | A | TCGA-HV-AA8X-01A-11D-A397-08 | TCGA-HV-AA8X-10A-01D-A39A-08 | g.chr2:152420121G>A | c.13589C>T | c.(13588-13590)gCg>gTg | p.A4530V |
| PAAD | 2 | 152420173 | 152420173 | + | Missense_Mutation | SNP | C | C | A | TCGA-HZ-A77Q-01A-11D-A36O-08 | TCGA-HZ-A77Q-10A-01D-A367-08 | g.chr2:152420173C>A | c.13537G>T | c.(13537-13539)Ggt>Tgt | p.G4513C |
| PAAD | 2 | 152466345 | 152466345 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-HZ-8637-01A-11D-2396-08 | TCGA-HZ-8637-10A-01D-2396-08 | g.chr2:152466345delT | c.11579delA | c.(11578-11580)aagfs | p.K3860fs |
| PAAD | 2 | 152466350 | 152466350 | + | Silent | SNP | T | T | C | TCGA-HZ-A8P0-01A-11D-A36O-08 | TCGA-HZ-A8P0-10A-01D-A367-08 | g.chr2:152466350T>C | c.11574A>G | c.(11572-11574)gcA>gcG | p.A3858A |
| PAAD | 2 | 152466579 | 152466579 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152466579C>T | c.11345G>A | c.(11344-11346)aGc>aAc | p.S3782N |
| PAAD | 2 | 152468847 | 152468847 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152468847G>A | c.10929C>T | c.(10927-10929)ggC>ggT | p.G3643G |
| PAAD | 2 | 152471039 | 152471039 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152471039C>A | c.10623G>T | c.(10621-10623)aaG>aaT | p.K3541N |
| PAAD | 2 | 152476229 | 152476229 | + | Silent | SNP | G | G | A | TCGA-FB-AAPP-01A-12D-A40W-08 | TCGA-FB-AAPP-11A-11D-A40W-08 | g.chr2:152476229G>A | c.9879C>T | c.(9877-9879)ggC>ggT | p.G3293G |
| PAAD | 2 | 152484296 | 152484296 | + | Missense_Mutation | SNP | C | C | A | TCGA-HZ-A77Q-01A-11D-A36O-08 | TCGA-HZ-A77Q-10A-01D-A367-08 | g.chr2:152484296C>A | c.9155G>T | c.(9154-9156)cGg>cTg | p.R3052L |
| PAAD | 2 | 152506868 | 152506868 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152506868C>T | c.7253G>A | c.(7252-7254)tGg>tAg | p.W2418* |
| PAAD | 2 | 152512680 | 152512680 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152512680C>T | c.6482G>A | c.(6481-6483)cGc>cAc | p.R2161H |
| PAAD | 2 | 152518831 | 152518831 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152518831C>T | c.5788G>A | c.(5788-5790)Gac>Aac | p.D1930N |
| PAAD | 2 | 152520341 | 152520341 | + | Missense_Mutation | SNP | T | T | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152520341T>G | c.5484A>C | c.(5482-5484)aaA>aaC | p.K1828N |
| PAAD | 2 | 152527556 | 152527556 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152527556T>C | c.4487A>G | c.(4486-4488)aAc>aGc | p.N1496S |
| PAAD | 2 | 152528985 | 152528985 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152528985G>A | c.4197C>T | c.(4195-4197)gtC>gtT | p.V1399V |
| PAAD | 2 | 152537333 | 152537333 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152537333G>A | c.2953C>T | c.(2953-2955)Cgc>Tgc | p.R985C |
| PAAD | 2 | 152552104 | 152552104 | + | Silent | SNP | A | A | G | TCGA-2J-AABR-01A-11D-A40W-08 | TCGA-2J-AABR-10A-01D-A40W-08 | g.chr2:152552104A>G | c.1662T>C | c.(1660-1662)taT>taC | p.Y554Y |
| PAAD | 2 | 152584236 | 152584236 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:152584236T>C | c.263A>G | c.(262-264)cAc>cGc | p.H88R |
| PAAD | 2 | 152586137 | 152586137 | + | Missense_Mutation | SNP | G | G | A | TCGA-LB-A7SX-01A-11D-A33T-08 | TCGA-LB-A7SX-10A-01D-A33W-08 | g.chr2:152586137G>A | c.70C>T | c.(70-72)Ccg>Tcg | p.P24S |
| PAAD | 2 | 152586146 | 152586146 | + | Missense_Mutation | SNP | C | C | G | TCGA-US-A77J-01A-11D-A32N-08 | TCGA-US-A77J-11A-11D-A32N-08 | g.chr2:152586146C>G | c.61G>C | c.(61-63)Gaa>Caa | p.E21Q |
| PCPG | 2 | 152466570 | 152466570 | + | Missense_Mutation | SNP | T | T | C | TCGA-WB-A81Q-01A-11D-A35I-08 | TCGA-WB-A81Q-10A-01D-A35G-08 | g.chr2:152466570T>C | c.11354A>G | c.(11353-11355)gAt>gGt | p.D3785G |
| PRAD | 2 | 152359340 | 152359340 | + | Silent | SNP | C | C | T | TCGA-VP-A87E-01A-31D-A34U-08 | TCGA-VP-A87E-10A-01D-A34X-08 | g.chr2:152359340C>T | c.18792G>A | c.(18790-18792)gaG>gaA | p.E6264E |
| PRAD | 2 | 152364588 | 152364588 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr2:152364588C>T | c.18279G>A | c.(18277-18279)tcG>tcA | p.S6093S |
| PRAD | 2 | 152381049 | 152381049 | + | Missense_Mutation | SNP | C | C | T | TCGA-KK-A8I6-01A-11D-A364-08 | TCGA-KK-A8I6-11A-12D-A362-08 | g.chr2:152381049C>T | c.17251G>A | c.(17251-17253)Gca>Aca | p.A5751T |
| PRAD | 2 | 152387573 | 152387573 | + | Missense_Mutation | SNP | A | A | C | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr2:152387573A>C | c.16462T>G | c.(16462-16464)Tac>Gac | p.Y5488D |
| PRAD | 2 | 152410424 | 152410424 | + | Missense_Mutation | SNP | C | C | T | TCGA-KK-A6E1-01A-11D-A30X-08 | TCGA-KK-A6E1-11A-21D-A30X-08 | g.chr2:152410424C>T | c.14441G>A | c.(14440-14442)cGc>cAc | p.R4814H |
| PRAD | 2 | 152420177 | 152420177 | + | Silent | SNP | C | C | G | TCGA-KK-A7AY-01A-11D-A33T-08 | TCGA-KK-A7AY-11A-21D-A33W-08 | g.chr2:152420177C>G | c.13533G>C | c.(13531-13533)gtG>gtC | p.V4511V |
| PRAD | 2 | 152474877 | 152474877 | + | Missense_Mutation | SNP | C | C | T | TCGA-EJ-AB27-01A-11D-A41K-08 | TCGA-EJ-AB27-10A-01D-A41N-08 | g.chr2:152474877C>T | c.10259G>A | c.(10258-10260)cGt>cAt | p.R3420H |
| PRAD | 2 | 152484040 | 152484040 | + | Silent | SNP | G | G | A | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr2:152484040G>A | c.9411C>T | c.(9409-9411)agC>agT | p.S3137S |
| PRAD | 2 | 152486104 | 152486104 | + | Missense_Mutation | SNP | A | A | T | TCGA-EJ-A65F-01A-21D-A30X-08 | TCGA-EJ-A65F-10A-01D-A30X-08 | g.chr2:152486104A>T | c.9051T>A | c.(9049-9051)agT>agA | p.S3017R |
| PRAD | 2 | 152490260 | 152490260 | + | Intron | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr2:152490260C>T | | | |
| PRAD | 2 | 152512437 | 152512437 | + | Missense_Mutation | SNP | G | G | A | TCGA-EJ-5542-01A-01D-1576-08 | TCGA-EJ-5542-10A-01D-1577-08 | g.chr2:152512437G>A | c.6596C>T | c.(6595-6597)gCc>gTc | p.A2199V |
| PRAD | 2 | 152515628 | 152515628 | + | Missense_Mutation | SNP | T | T | C | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr2:152515628T>C | c.6026A>G | c.(6025-6027)gAt>gGt | p.D2009G |
| PRAD | 2 | 152521933 | 152521933 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-EJ-7784-01A-11D-2114-08 | TCGA-EJ-7784-10A-01D-2114-08 | g.chr2:152521933delG | c.5152delC | c.(5152-5154)cagfs | p.Q1718fs |
| PRAD | 2 | 152529086 | 152529086 | + | Missense_Mutation | SNP | A | A | G | TCGA-X4-A8KQ-01A-12D-A364-08 | TCGA-X4-A8KQ-10A-01D-A362-08 | g.chr2:152529086A>G | c.4096T>C | c.(4096-4098)Tct>Cct | p.S1366P |
| READ | 2 | 152349881 | 152349881 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152349881C>A | c.19183G>T | c.(19183-19185)Gaa>Taa | p.E6395* |
| READ | 2 | 152350697 | 152350697 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152350697C>T | c.18989G>A | c.(18988-18990)cGc>cAc | p.R6330H |
| READ | 2 | 152359931 | 152359931 | + | Missense_Mutation | SNP | T | T | C | TCGA-AF-6672-01A-11D-1826-10 | TCGA-AF-6672-10A-01D-1826-10 | g.chr2:152359931T>C | c.18664A>G | c.(18664-18666)Aca>Gca | p.T6222A |
| READ | 2 | 152375525 | 152375525 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152375525G>T | c.17546C>A | c.(17545-17547)tCt>tAt | p.S5849Y |
| READ | 2 | 152376261 | 152376261 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152376261C>T | c.17398G>A | c.(17398-17400)Gat>Aat | p.D5800N |
| READ | 2 | 152380919 | 152380919 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152380919C>A | c.17282G>T | c.(17281-17283)aGa>aTa | p.R5761I |
| READ | 2 | 152381773 | 152381773 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152381773C>A | c.17073G>T | c.(17071-17073)aaG>aaT | p.K5691N |
| READ | 2 | 152390743 | 152390743 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152390743C>T | c.16300G>A | c.(16300-16302)Gac>Aac | p.D5434N |
| READ | 2 | 152390749 | 152390749 | + | Missense_Mutation | SNP | C | C | T | TCGA-DC-6158-01A-11D-1657-10 | TCGA-DC-6158-10A-01D-1657-10 | g.chr2:152390749C>T | c.16294G>A | c.(16294-16296)Gca>Aca | p.A5432T |
| READ | 2 | 152393738 | 152393738 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr2:152393738C>A | c.16012G>T | c.(16012-16014)Gaa>Taa | p.E5338* |
| READ | 2 | 152402489 | 152402489 | + | Silent | SNP | C | C | T | TCGA-DC-6682-01A-11D-1826-10 | TCGA-DC-6682-10A-01D-1826-10 | g.chr2:152402489C>T | c.15387G>A | c.(15385-15387)aaG>aaA | p.K5129K |
| READ | 2 | 152406166 | 152406166 | + | Missense_Mutation | SNP | C | C | T | TCGA-AF-6672-01A-11D-1826-10 | TCGA-AF-6672-10A-01D-1826-10 | g.chr2:152406166C>T | c.14930G>A | c.(14929-14931)cGt>cAt | p.R4977H |
| READ | 2 | 152419150 | 152419150 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152419150C>T | c.13763G>A | c.(13762-13764)cGa>cAa | p.R4588Q |
| READ | 2 | 152423966 | 152423966 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152423966G>A | c.12769C>T | c.(12769-12771)Caa>Taa | p.Q4257* |
| READ | 2 | 152472613 | 152472613 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152472613T>G | c.10463A>C | c.(10462-10464)aAa>aCa | p.K3488T |
| READ | 2 | 152484275 | 152484275 | + | Missense_Mutation | SNP | T | T | C | TCGA-DY-A1DF-01A-11D-A152-10 | TCGA-DY-A1DF-10A-01D-A152-10 | g.chr2:152484275T>C | c.9176A>G | c.(9175-9177)aAg>aGg | p.K3059R |
| READ | 2 | 152500443 | 152500443 | + | Silent | SNP | G | G | A | TCGA-AG-4005-01A-01W-1073-09 | TCGA-AG-4005-10A-01W-1073-09 | g.chr2:152500443G>A | c.7845C>T | c.(7843-7845)tgC>tgT | p.C2615C |
| READ | 2 | 152501066 | 152501066 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152501066C>A | c.7560G>T | c.(7558-7560)gaG>gaT | p.E2520D |
| READ | 2 | 152502747 | 152502747 | + | Splice_Site | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152502747C>T | c.7433G>A | c.(7432-7434)aGa>aAa | p.R2478K |
| READ | 2 | 152506778 | 152506778 | + | Missense_Mutation | SNP | C | C | T | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr2:152506778C>T | c.7343G>A | c.(7342-7344)cGt>cAt | p.R2448H |
| READ | 2 | 152506794 | 152506794 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A01W-01A-21W-A096-10 | TCGA-AG-A01W-11A-11W-A096-10 | g.chr2:152506794T>G | c.7327A>C | c.(7327-7329)Agt>Cgt | p.S2443R |
| READ | 2 | 152512413 | 152512413 | + | Missense_Mutation | SNP | T | T | C | TCGA-DY-A1DG-01A-11D-A152-10 | TCGA-DY-A1DG-10A-01D-A152-10 | g.chr2:152512413T>C | c.6620A>G | c.(6619-6621)cAc>cGc | p.H2207R |
| READ | 2 | 152518760 | 152518760 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152518760C>A | c.5859G>T | c.(5857-5859)gaG>gaT | p.E1953D |
| READ | 2 | 152522908 | 152522908 | + | Missense_Mutation | SNP | T | T | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr2:152522908T>C | c.4727A>G | c.(4726-4728)tAt>tGt | p.Y1576C |
| READ | 2 | 152554088 | 152554088 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152554088G>A | c.1227C>T | c.(1225-1227)ctC>ctT | p.L409L |
| READ | 2 | 152566209 | 152566209 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:152566209C>A | c.996G>T | c.(994-996)gaG>gaT | p.E332D |
| READ | 2 | 152582047 | 152582047 | + | Missense_Mutation | SNP | T | T | C | TCGA-DT-5265-01A-21D-1826-10 | TCGA-DT-5265-10A-01D-1826-10 | g.chr2:152582047T>C | c.322A>G | c.(322-324)Aca>Gca | p.T108A |
| SARC | 2 | 152381747 | 152381747 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr2:152381747G>A | c.17099C>T | c.(17098-17100)tCc>tTc | p.S5700F |
| SARC | 2 | 152425138 | 152425138 | + | Silent | SNP | G | G | A | TCGA-DX-A48R-01A-11D-A307-09 | TCGA-DX-A48R-10A-01D-A307-09 | g.chr2:152425138G>A | c.12525C>T | c.(12523-12525)ctC>ctT | p.L4175L |
| SARC | 2 | 152426886 | 152426886 | + | Silent | SNP | A | A | G | TCGA-IW-A3M6-01A-11D-A21Q-09 | TCGA-IW-A3M6-10A-01D-A21Q-09 | g.chr2:152426886A>G | c.12036T>C | c.(12034-12036)caT>caC | p.H4012H |
| SARC | 2 | 152463201 | 152463201 | + | Intron | SNP | G | G | A | TCGA-DX-A23R-01A-11D-A26G-09 | TCGA-DX-A23R-10A-01D-A26G-09 | g.chr2:152463201G>A | | | |
| SARC | 2 | 152477456 | 152477456 | + | Missense_Mutation | SNP | C | C | T | TCGA-DX-A8BP-01A-11D-A37C-09 | TCGA-DX-A8BP-10A-01D-A37F-09 | g.chr2:152477456C>T | c.9808G>A | c.(9808-9810)Gcc>Acc | p.A3270T |
| SARC | 2 | 152477457 | 152477457 | + | Silent | SNP | C | C | T | TCGA-DX-A8BP-01A-11D-A37C-09 | TCGA-DX-A8BP-10A-01D-A37F-09 | g.chr2:152477457C>T | c.9807G>A | c.(9805-9807)aaG>aaA | p.K3269K |
| SARC | 2 | 152512421 | 152512421 | + | Silent | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr2:152512421G>A | c.6612C>T | c.(6610-6612)taC>taT | p.Y2204Y |
| SARC | 2 | 152512817 | 152512817 | + | Silent | SNP | G | G | T | TCGA-K1-A6RT-01A-32D-A33E-09 | TCGA-K1-A6RT-10A-01D-A33H-09 | g.chr2:152512817G>T | c.6345C>A | c.(6343-6345)acC>acA | p.T2115T |
| SARC | 2 | 152521285 | 152521285 | + | Silent | SNP | G | G | A | TCGA-PT-A8TR-01A-11D-A37C-09 | TCGA-PT-A8TR-10A-01D-A37F-09 | g.chr2:152521285G>A | c.5331C>T | c.(5329-5331)atC>atT | p.I1777I |
| SARC | 2 | 152521285 | 152521285 | + | Silent | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr2:152521285G>A | c.5331C>T | c.(5329-5331)atC>atT | p.I1777I |
| SARC | 2 | 152521904 | 152521904 | + | Silent | SNP | G | G | A | TCGA-HB-A2OT-01A-11D-A21Q-09 | TCGA-HB-A2OT-10A-01D-A21Q-09 | g.chr2:152521904G>A | c.5181C>T | c.(5179-5181)taC>taT | p.Y1727Y |
| SARC | 2 | 152527713 | 152527713 | + | Silent | SNP | A | A | G | TCGA-X6-A7WD-01A-21D-A351-09 | TCGA-X6-A7WD-10A-01D-A351-09 | g.chr2:152527713A>G | c.4330T>C | c.(4330-4332)Ttg>Ctg | p.L1444L |
| SARC | 2 | 152548372 | 152548377 | + | Splice_Site | DEL | ACTTAC | ACTTAC | - | TCGA-QQ-A5V9-01A-11D-A32I-09 | TCGA-QQ-A5V9-11A-31D-A32I-09 | g.chr2:152548372_152548377delACTTAC | | c.e23+1 | |
| SARC | 2 | 152581369 | 152581369 | + | Splice_Site | SNP | A | A | C | TCGA-MO-A47R-01A-11D-A24N-09 | TCGA-MO-A47R-10A-01D-A24N-09 | g.chr2:152581369A>C | | c.e7+1 | |
| SARC | 2 | 152582033 | 152582033 | + | Silent | SNP | T | T | G | TCGA-DX-A8BU-01A-11D-A37C-09 | TCGA-DX-A8BU-10A-01D-A37F-09 | g.chr2:152582033T>G | c.336A>C | c.(334-336)ccA>ccC | p.P112P |
| SKCM | 2 | 152342309 | 152342309 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr2:152342309C>T | c.19975G>A | c.(19975-19977)Gga>Aga | p.G6659R |
| SKCM | 2 | 152348943 | 152348943 | + | Silent | SNP | G | G | A | TCGA-DA-A1IA-06A-11D-A196-08 | TCGA-DA-A1IA-10A-01D-A198-08 | g.chr2:152348943G>A | c.19263C>T | c.(19261-19263)ccC>ccT | p.P6421P |
| SKCM | 2 | 152348944 | 152348944 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1IA-06A-11D-A196-08 | TCGA-DA-A1IA-10A-01D-A198-08 | g.chr2:152348944G>A | c.19262C>T | c.(19261-19263)cCc>cTc | p.P6421L |
| SKCM | 2 | 152349000 | 152349001 | + | Frame_Shift_Del | DEL | AT | AT | - | TCGA-D3-A5GS-06A-11D-A27K-08 | TCGA-D3-A5GS-10A-01D-A27N-08 | g.chr2:152349000_152349001delAT | c.19205_19206delAT | c.(19204-19206)tatfs | p.Y6402fs |
| SKCM | 2 | 152350316 | 152350316 | + | Silent | SNP | C | C | T | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr2:152350316C>T | c.19077G>A | c.(19075-19077)gtG>gtA | p.V6359V |
| SKCM | 2 | 152352862 | 152352862 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:152352862C>T | c.18846G>A | c.(18844-18846)atG>atA | p.M6282I |
| SKCM | 2 | 152352869 | 152352869 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:152352869T>A | c.18839A>T | c.(18838-18840)gAa>gTa | p.E6280V |
| SKCM | 2 | 152354181 | 152354181 | + | Intron | SNP | C | C | T | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr2:152354181C>T | | | |
| SKCM | 2 | 152359376 | 152359376 | + | Silent | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr2:152359376C>T | c.18756G>A | c.(18754-18756)ggG>ggA | p.G6252G |
| SKCM | 2 | 152359377 | 152359377 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZA-06A-11D-A197-08 | TCGA-FS-A1ZA-10A-01D-A199-08 | g.chr2:152359377C>T | c.18755G>A | c.(18754-18756)gGg>gAg | p.G6252E |
| SKCM | 2 | 152369315 | 152369315 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A183-06A-11D-A196-08 | TCGA-EE-A183-10A-01D-A198-08 | g.chr2:152369315T>C | c.18175A>G | c.(18175-18177)Aat>Gat | p.N6059D |
| SKCM | 2 | 152370118 | 152370118 | + | Silent | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152370118C>T | c.18114G>A | c.(18112-18114)agG>agA | p.R6038R |
| SKCM | 2 | 152370931 | 152370931 | + | Silent | SNP | C | C | T | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chr2:152370931C>T | c.17925G>A | c.(17923-17925)agG>agA | p.R5975R |
| SKCM | 2 | 152373030 | 152373030 | + | Silent | SNP | C | C | T | TCGA-EE-A183-06A-11D-A196-08 | TCGA-EE-A183-10A-01D-A198-08 | g.chr2:152373030C>T | c.17745G>A | c.(17743-17745)ctG>ctA | p.L5915L |
| SKCM | 2 | 152374874 | 152374874 | + | Silent | SNP | C | C | T | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr2:152374874C>T | c.17655G>A | c.(17653-17655)ctG>ctA | p.L5885L |
| SKCM | 2 | 152376255 | 152376255 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr2:152376255C>T | c.17404G>A | c.(17404-17406)Gaa>Aaa | p.E5802K |
| SKCM | 2 | 152381753 | 152381753 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152381753C>T | c.17093G>A | c.(17092-17094)gGa>gAa | p.G5698E |
| SKCM | 2 | 152381774 | 152381774 | + | Missense_Mutation | SNP | T | T | A | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr2:152381774T>A | c.17072A>T | c.(17071-17073)aAg>aTg | p.K5691M |
| SKCM | 2 | 152382699 | 152382699 | + | Silent | SNP | C | C | T | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr2:152382699C>T | c.16920G>A | c.(16918-16920)gcG>gcA | p.A5640A |
| SKCM | 2 | 152384066 | 152384066 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A4U4-06A-11D-A32N-08 | TCGA-GN-A4U4-10B-01D-A32N-08 | g.chr2:152384066C>T | c.16666G>A | c.(16666-16668)Gcc>Acc | p.A5556T |
| SKCM | 2 | 152388399 | 152388399 | + | Silent | SNP | C | C | T | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr2:152388399C>T | c.16326G>A | c.(16324-16326)agG>agA | p.R5442R |
| SKCM | 2 | 152394450 | 152394450 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152394450C>T | c.15935G>A | c.(15934-15936)tGg>tAg | p.W5312* |
| SKCM | 2 | 152394723 | 152394723 | + | Silent | SNP | C | C | T | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr2:152394723C>T | c.15825G>A | c.(15823-15825)ggG>ggA | p.G5275G |
| SKCM | 2 | 152397999 | 152397999 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:152397999G>A | c.15541C>T | c.(15541-15543)Ctt>Ttt | p.L5181F |
| SKCM | 2 | 152402475 | 152402475 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152402475C>T | c.15401G>A | c.(15400-15402)cGa>cAa | p.R5134Q |
| SKCM | 2 | 152404006 | 152404006 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr2:152404006C>T | c.15201G>A | c.(15199-15201)atG>atA | p.M5067I |
| SKCM | 2 | 152404158 | 152404158 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A2NH-06A-11D-A196-08 | TCGA-ER-A2NH-10A-01D-A198-08 | g.chr2:152404158G>A | c.15149C>T | c.(15148-15150)gCt>gTt | p.A5050V |
| SKCM | 2 | 152404231 | 152404231 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr2:152404231G>A | c.15076C>T | c.(15076-15078)Cac>Tac | p.H5026Y |
| SKCM | 2 | 152404824 | 152404824 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A183-06A-11D-A196-08 | TCGA-EE-A183-10A-01D-A198-08 | g.chr2:152404824C>T | c.15052G>A | c.(15052-15054)Gag>Aag | p.E5018K |
| SKCM | 2 | 152404847 | 152404847 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr2:152404847C>T | c.15029G>A | c.(15028-15030)cGg>cAg | p.R5010Q |
| SKCM | 2 | 152404848 | 152404848 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19N-06A-11D-A197-08 | TCGA-ER-A19N-10A-01D-A199-08 | g.chr2:152404848G>A | c.15028C>T | c.(15028-15030)Cgg>Tgg | p.R5010W |
| SKCM | 2 | 152408283 | 152408283 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MQ-06A-11D-A197-08 | TCGA-EE-A2MQ-10A-01D-A199-08 | g.chr2:152408283C>T | c.14810G>A | c.(14809-14811)cGg>cAg | p.R4937Q |
| SKCM | 2 | 152409917 | 152409917 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr2:152409917C>T | c.14623G>A | c.(14623-14625)Gat>Aat | p.D4875N |
| SKCM | 2 | 152410366 | 152410366 | + | Silent | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:152410366C>T | c.14499G>A | c.(14497-14499)agG>agA | p.R4833R |
| SKCM | 2 | 152410392 | 152410392 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152410392C>T | c.14473G>A | c.(14473-14475)Gac>Aac | p.D4825N |
| SKCM | 2 | 152410454 | 152410454 | + | Missense_Mutation | SNP | G | G | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr2:152410454G>T | c.14411C>A | c.(14410-14412)tCc>tAc | p.S4804Y |
| SKCM | 2 | 152410459 | 152410459 | + | Silent | SNP | C | C | T | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr2:152410459C>T | c.14406G>A | c.(14404-14406)aaG>aaA | p.K4802K |
| SKCM | 2 | 152417610 | 152417610 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr2:152417610C>T | c.14011G>A | c.(14011-14013)Gaa>Aaa | p.E4671K |
| SKCM | 2 | 152418643 | 152418643 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr2:152418643G>A | c.13874C>T | c.(13873-13875)tCa>tTa | p.S4625L |
| SKCM | 2 | 152419197 | 152419197 | + | Silent | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:152419197G>A | c.13716C>T | c.(13714-13716)ttC>ttT | p.F4572F |
| SKCM | 2 | 152419208 | 152419208 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-GF-A4EO-06A-12D-A24R-08 | TCGA-GF-A4EO-10A-01D-A24R-08 | g.chr2:152419208G>A | c.13705C>T | c.(13705-13707)Cga>Tga | p.R4569* |
| SKCM | 2 | 152420119 | 152420119 | + | Splice_Site | SNP | C | C | T | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr2:152420119C>T | | c.e91+1 | |
| SKCM | 2 | 152420200 | 152420200 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:152420200C>T | c.13510G>A | c.(13510-13512)Ggt>Agt | p.G4504S |
| SKCM | 2 | 152420423 | 152420423 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr2:152420423C>T | c.13390G>A | c.(13390-13392)Gag>Aag | p.E4464K |
| SKCM | 2 | 152420431 | 152420431 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr2:152420431C>T | c.13382G>A | c.(13381-13383)gGg>gAg | p.G4461E |
| SKCM | 2 | 152421650 | 152421650 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:152421650C>T | c.13276G>A | c.(13276-13278)Gaa>Aaa | p.E4426K |
| SKCM | 2 | 152422108 | 152422108 | + | Silent | SNP | C | C | T | TCGA-ER-A19E-06A-11D-A197-08 | TCGA-ER-A19E-10A-01D-A199-08 | g.chr2:152422108C>T | c.13170G>A | c.(13168-13170)aaG>aaA | p.K4390K |
| SKCM | 2 | 152422239 | 152422239 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1I1-06A-12D-A196-08 | TCGA-DA-A1I1-10A-01D-A198-08 | g.chr2:152422239C>T | c.13149G>A | c.(13147-13149)atG>atA | p.M4383I |
| SKCM | 2 | 152422268 | 152422268 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:152422268G>A | c.13120C>T | c.(13120-13122)Cat>Tat | p.H4374Y |
| SKCM | 2 | 152423746 | 152423746 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152423746C>T | c.12989G>A | c.(12988-12990)tGg>tAg | p.W4330* |
| SKCM | 2 | 152423779 | 152423779 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr2:152423779C>T | c.12956G>A | c.(12955-12957)aGt>aAt | p.S4319N |
| SKCM | 2 | 152424920 | 152424920 | + | Silent | SNP | C | C | T | TCGA-EE-A2M6-06A-12D-A197-08 | TCGA-EE-A2M6-10A-01D-A199-08 | g.chr2:152424920C>T | c.12543G>A | c.(12541-12543)cgG>cgA | p.R4181R |
| SKCM | 2 | 152424922 | 152424922 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr2:152424922G>A | c.12541C>T | c.(12541-12543)Cgg>Tgg | p.R4181W |
| SKCM | 2 | 152424923 | 152424923 | + | Silent | SNP | G | G | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr2:152424923G>A | c.12540C>T | c.(12538-12540)taC>taT | p.Y4180Y |
| SKCM | 2 | 152425865 | 152425865 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr2:152425865C>T | c.12349G>A | c.(12349-12351)Gaa>Aaa | p.E4117K |
| SKCM | 2 | 152426609 | 152426609 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1I1-06A-12D-A196-08 | TCGA-DA-A1I1-10A-01D-A198-08 | g.chr2:152426609C>T | c.12313G>A | c.(12313-12315)Gaa>Aaa | p.E4105K |
| SKCM | 2 | 152426609 | 152426609 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr2:152426609C>T | c.12313G>A | c.(12313-12315)Gaa>Aaa | p.E4105K |
| SKCM | 2 | 152426748 | 152426748 | + | Silent | SNP | C | C | T | TCGA-FS-A4F5-06A-11D-A25O-08 | TCGA-FS-A4F5-10B-01D-A25O-08 | g.chr2:152426748C>T | c.12174G>A | c.(12172-12174)caG>caA | p.Q4058Q |
| SKCM | 2 | 152426873 | 152426873 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A4EO-06A-12D-A24R-08 | TCGA-GF-A4EO-10A-01D-A24R-08 | g.chr2:152426873C>T | c.12049G>A | c.(12049-12051)Gga>Aga | p.G4017R |
| SKCM | 2 | 152427047 | 152427047 | + | Silent | SNP | G | G | A | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr2:152427047G>A | c.11979C>T | c.(11977-11979)atC>atT | p.I3993I |
| SKCM | 2 | 152432234 | 152432234 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr2:152432234C>T | c.11885G>A | c.(11884-11886)aGa>aAa | p.R3962K |
| SKCM | 2 | 152432249 | 152432249 | + | Missense_Mutation | SNP | T | T | G | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152432249T>G | c.11870A>C | c.(11869-11871)gAa>gCa | p.E3957A |
| SKCM | 2 | 152432772 | 152432772 | + | Missense_Mutation | SNP | A | A | T | TCGA-FW-A3TV-06A-11D-A23B-08 | TCGA-FW-A3TV-10A-01D-A23B-08 | g.chr2:152432772A>T | c.11698T>A | c.(11698-11700)Ttt>Att | p.F3900I |
| SKCM | 2 | 152432773 | 152432773 | + | Silent | SNP | G | G | A | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr2:152432773G>A | c.11697C>T | c.(11695-11697)atC>atT | p.I3899I |
| SKCM | 2 | 152432773 | 152432773 | + | Silent | SNP | G | G | A | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr2:152432773G>A | c.11697C>T | c.(11695-11697)atC>atT | p.I3899I |
| SKCM | 2 | 152432838 | 152432838 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A5GR-06A-11D-A27K-08 | TCGA-D3-A5GR-10A-01D-A27N-08 | g.chr2:152432838G>A | c.11632C>T | c.(11632-11634)Cgt>Tgt | p.R3878C |
| SKCM | 2 | 152466492 | 152466492 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr2:152466492C>T | c.11432G>A | c.(11431-11433)tGg>tAg | p.W3811* |
| SKCM | 2 | 152466568 | 152466568 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr2:152466568C>T | c.11356G>A | c.(11356-11358)Gat>Aat | p.D3786N |
| SKCM | 2 | 152467039 | 152467039 | + | Silent | SNP | G | G | A | TCGA-ER-A19W-06A-41D-A23B-08 | TCGA-ER-A19W-10A-01D-A23B-08 | g.chr2:152467039G>A | c.11280C>T | c.(11278-11280)atC>atT | p.I3760I |
| SKCM | 2 | 152468714 | 152468714 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152468714G>A | c.11062C>T | c.(11062-11064)Ctg>Ttg | p.L3688L |
| SKCM | 2 | 152470822 | 152470822 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152470822G>A | c.10840C>T | c.(10840-10842)Cag>Tag | p.Q3614* |
| SKCM | 2 | 152470873 | 152470873 | + | Missense_Mutation | SNP | T | T | C | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr2:152470873T>C | c.10789A>G | c.(10789-10791)Aag>Gag | p.K3597E |
| SKCM | 2 | 152471012 | 152471012 | + | Silent | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr2:152471012G>A | c.10650C>T | c.(10648-10650)atC>atT | p.I3550I |
| SKCM | 2 | 152471030 | 152471030 | + | Silent | SNP | C | C | T | TCGA-D3-A2JN-06A-11D-A196-08 | TCGA-D3-A2JN-10A-01D-A198-08 | g.chr2:152471030C>T | c.10632G>A | c.(10630-10632)ccG>ccA | p.P3544P |
| SKCM | 2 | 152472610 | 152472610 | + | Missense_Mutation | SNP | A | A | C | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:152472610A>C | c.10466T>G | c.(10465-10467)cTt>cGt | p.L3489R |
| SKCM | 2 | 152474840 | 152474840 | + | Silent | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr2:152474840C>T | c.10296G>A | c.(10294-10296)acG>acA | p.T3432T |
| SKCM | 2 | 152474902 | 152474902 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3MU-06A-11D-A21A-08 | TCGA-D3-A3MU-10A-01D-A21A-08 | g.chr2:152474902C>T | c.10234G>A | c.(10234-10236)Gaa>Aaa | p.E3412K |
| SKCM | 2 | 152482132 | 152482132 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A17X-06A-11D-A197-08 | TCGA-EE-A17X-10A-01D-A199-08 | g.chr2:152482132C>T | c.9639G>A | c.(9637-9639)tgG>tgA | p.W3213* |
| SKCM | 2 | 152483634 | 152483634 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152483634G>A | c.9500C>T | c.(9499-9501)gCt>gTt | p.A3167V |
| SKCM | 2 | 152483671 | 152483671 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:152483671G>A | c.9463C>T | c.(9463-9465)Ccc>Tcc | p.P3155S |
| SKCM | 2 | 152484039 | 152484039 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GB-06A-11D-A197-08 | TCGA-EE-A2GB-10A-01D-A199-08 | g.chr2:152484039C>T | c.9412G>A | c.(9412-9414)Gat>Aat | p.D3138N |
| SKCM | 2 | 152484119 | 152484119 | + | Missense_Mutation | SNP | T | T | C | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:152484119T>C | c.9332A>G | c.(9331-9333)aAg>aGg | p.K3111R |
| SKCM | 2 | 152484210 | 152484210 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr2:152484210T>A | c.9241A>T | c.(9241-9243)Aag>Tag | p.K3081* |
| SKCM | 2 | 152484282 | 152484282 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr2:152484282C>T | c.9169G>A | c.(9169-9171)Gac>Aac | p.D3057N |
| SKCM | 2 | 152490301 | 152490301 | + | Intron | SNP | C | C | T | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr2:152490301C>T | | | |
| SKCM | 2 | 152490354 | 152490354 | + | Intron | SNP | T | T | C | TCGA-FS-A1ZM-06A-12D-A197-08 | TCGA-FS-A1ZM-10A-01D-A199-08 | g.chr2:152490354T>C | | | |
| SKCM | 2 | 152490363 | 152490363 | + | Intron | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr2:152490363C>T | | | |
| SKCM | 2 | 152490375 | 152490375 | + | Intron | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152490375G>A | | | |
| SKCM | 2 | 152490409 | 152490409 | + | Intron | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152490409G>A | | | |
| SKCM | 2 | 152492815 | 152492815 | + | Intron | SNP | T | T | G | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr2:152492815T>G | | | |
| SKCM | 2 | 152492816 | 152492816 | + | Intron | SNP | C | C | T | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr2:152492816C>T | | | |
| SKCM | 2 | 152496516 | 152496516 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3MU-06A-11D-A21A-08 | TCGA-D3-A3MU-10A-01D-A21A-08 | g.chr2:152496516G>A | c.8744C>T | c.(8743-8745)tCt>tTt | p.S2915F |
| SKCM | 2 | 152496526 | 152496526 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-FS-A1ZE-06A-11D-A197-08 | TCGA-FS-A1ZE-10A-01D-A199-08 | g.chr2:152496526delA | c.8734delT | c.(8734-8736)tccfs | p.S2912fs |
| SKCM | 2 | 152496542 | 152496542 | + | Silent | SNP | T | T | C | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:152496542T>C | c.8718A>G | c.(8716-8718)agA>agG | p.R2906R |
| SKCM | 2 | 152496875 | 152496875 | + | Silent | SNP | C | C | T | TCGA-ER-A19G-06A-11D-A196-08 | TCGA-ER-A19G-10A-01D-A198-08 | g.chr2:152496875C>T | c.8679G>A | c.(8677-8679)caG>caA | p.Q2893Q |
| SKCM | 2 | 152496920 | 152496920 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152496920G>A | c.8634C>T | c.(8632-8634)ccC>ccT | p.P2878P |
| SKCM | 2 | 152496921 | 152496921 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2JF-06A-11D-A196-08 | TCGA-D3-A2JF-10A-01D-A198-08 | g.chr2:152496921G>A | c.8633C>T | c.(8632-8634)cCc>cTc | p.P2878L |
| SKCM | 2 | 152496921 | 152496921 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152496921G>A | c.8633C>T | c.(8632-8634)cCc>cTc | p.P2878L |
| SKCM | 2 | 152497000 | 152497000 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2ML-06A-11D-A197-08 | TCGA-EE-A2ML-10A-01D-A199-08 | g.chr2:152497000C>T | c.8554G>A | c.(8554-8556)Gtg>Atg | p.V2852M |
| SKCM | 2 | 152497159 | 152497159 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr2:152497159G>A | c.8395C>T | c.(8395-8397)Cgt>Tgt | p.R2799C |
| SKCM | 2 | 152499129 | 152499129 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr2:152499129G>A | c.8332C>T | c.(8332-8334)Cct>Tct | p.P2778S |
| SKCM | 2 | 152499715 | 152499715 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr2:152499715C>T | c.8109G>A | c.(8107-8109)atG>atA | p.M2703I |
| SKCM | 2 | 152499777 | 152499777 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr2:152499777G>A | c.8047C>T | c.(8047-8049)Cag>Tag | p.Q2683* |
| SKCM | 2 | 152499804 | 152499804 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152499804C>T | c.8020G>A | c.(8020-8022)Gag>Aag | p.E2674K |
| SKCM | 2 | 152500364 | 152500364 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr2:152500364G>A | c.7924C>T | c.(7924-7926)Cat>Tat | p.H2642Y |
| SKCM | 2 | 152500373 | 152500373 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr2:152500373C>T | c.7915G>A | c.(7915-7917)Gat>Aat | p.D2639N |
| SKCM | 2 | 152500476 | 152500476 | + | Silent | SNP | C | C | T | TCGA-EE-A20H-06A-11D-A197-08 | TCGA-EE-A20H-10A-01D-A199-08 | g.chr2:152500476C>T | c.7812G>A | c.(7810-7812)gtG>gtA | p.V2604V |
| SKCM | 2 | 152500514 | 152500514 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1I8-06A-11D-A197-08 | TCGA-DA-A1I8-10A-01D-A199-08 | g.chr2:152500514C>T | c.7774G>A | c.(7774-7776)Gac>Aac | p.D2592N |
| SKCM | 2 | 152500515 | 152500515 | + | Silent | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:152500515C>T | c.7773G>A | c.(7771-7773)aaG>aaA | p.K2591K |
| SKCM | 2 | 152500560 | 152500560 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D9-A3Z1-06A-11D-A23B-08 | TCGA-D9-A3Z1-10A-01D-A23B-08 | g.chr2:152500560C>T | c.7728G>A | c.(7726-7728)tgG>tgA | p.W2576* |
| SKCM | 2 | 152500622 | 152500622 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr2:152500622G>A | c.7666C>T | c.(7666-7668)Cgc>Tgc | p.R2556C |
| SKCM | 2 | 152500996 | 152500996 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr2:152500996C>T | c.7630G>A | c.(7630-7632)Gaa>Aaa | p.E2544K |
| SKCM | 2 | 152501044 | 152501044 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MT-06A-11D-A197-08 | TCGA-EE-A2MT-10A-01D-A199-08 | g.chr2:152501044C>T | c.7582G>A | c.(7582-7584)Gat>Aat | p.D2528N |
| SKCM | 2 | 152506743 | 152506743 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr2:152506743G>A | c.7378C>T | c.(7378-7380)Cct>Tct | p.P2460S |
| SKCM | 2 | 152506779 | 152506779 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19A-06A-21D-A197-08 | TCGA-ER-A19A-10A-01D-A199-08 | g.chr2:152506779G>A | c.7342C>T | c.(7342-7344)Cgt>Tgt | p.R2448C |
| SKCM | 2 | 152506828 | 152506828 | + | Silent | SNP | C | C | T | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr2:152506828C>T | c.7293G>A | c.(7291-7293)gaG>gaA | p.E2431E |
| SKCM | 2 | 152506845 | 152506845 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A183-06A-11D-A196-08 | TCGA-EE-A183-10A-01D-A198-08 | g.chr2:152506845G>A | c.7276C>T | c.(7276-7278)Ccc>Tcc | p.P2426S |
| SKCM | 2 | 152506890 | 152506890 | + | Silent | SNP | G | G | A | TCGA-ER-A19M-06A-61D-A23B-08 | TCGA-ER-A19M-10A-01D-A23B-08 | g.chr2:152506890G>A | c.7231C>T | c.(7231-7233)Cta>Tta | p.L2411L |
| SKCM | 2 | 152507129 | 152507129 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr2:152507129C>T | c.7186G>A | c.(7186-7188)Gat>Aat | p.D2396N |
| SKCM | 2 | 152507129 | 152507129 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr2:152507129C>T | c.7186G>A | c.(7186-7188)Gat>Aat | p.D2396N |
| SKCM | 2 | 152507129 | 152507129 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152507129C>T | c.7186G>A | c.(7186-7188)Gat>Aat | p.D2396N |
| SKCM | 2 | 152507246 | 152507246 | + | Missense_Mutation | SNP | A | A | T | TCGA-FS-A1ZD-06A-11D-A197-08 | TCGA-FS-A1ZD-10A-01D-A199-08 | g.chr2:152507246A>T | c.7069T>A | c.(7069-7071)Ttc>Atc | p.F2357I |
| SKCM | 2 | 152507370 | 152507370 | + | Silent | SNP | T | T | C | TCGA-EE-A3AF-06A-11D-A196-08 | TCGA-EE-A3AF-10A-01D-A198-08 | g.chr2:152507370T>C | c.6945A>G | c.(6943-6945)caA>caG | p.Q2315Q |
| SKCM | 2 | 152507377 | 152507377 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr2:152507377C>T | c.6938G>A | c.(6937-6939)cGa>cAa | p.R2313Q |
| SKCM | 2 | 152507377 | 152507377 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152507377C>T | c.6938G>A | c.(6937-6939)cGa>cAa | p.R2313Q |
| SKCM | 2 | 152510568 | 152510568 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr2:152510568C>T | c.6853G>A | c.(6853-6855)Gat>Aat | p.D2285N |
| SKCM | 2 | 152510568 | 152510568 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MN-06A-11D-A197-08 | TCGA-EE-A2MN-10A-01D-A199-08 | g.chr2:152510568C>T | c.6853G>A | c.(6853-6855)Gat>Aat | p.D2285N |
| SKCM | 2 | 152510592 | 152510592 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6E9-06A-12D-A30X-08 | TCGA-D9-A6E9-10A-01D-A30X-08 | g.chr2:152510592C>T | c.6829G>A | c.(6829-6831)Gaa>Aaa | p.E2277K |
| SKCM | 2 | 152512464 | 152512464 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A2MH-06A-11D-A197-08 | TCGA-EE-A2MH-10A-01D-A199-08 | g.chr2:152512464T>C | c.6569A>G | c.(6568-6570)gAg>gGg | p.E2190G |
| SKCM | 2 | 152512466 | 152512466 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr2:152512466C>T | c.6567G>A | c.(6565-6567)gtG>gtA | p.V2189V |
| SKCM | 2 | 152512673 | 152512673 | + | Silent | SNP | C | C | T | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr2:152512673C>T | c.6489G>A | c.(6487-6489)caG>caA | p.Q2163Q |
| SKCM | 2 | 152512757 | 152512757 | + | Silent | SNP | A | A | G | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:152512757A>G | c.6405T>C | c.(6403-6405)acT>acC | p.T2135T |
| SKCM | 2 | 152512872 | 152512872 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr2:152512872T>C | c.6290A>G | c.(6289-6291)cAa>cGa | p.Q2097R |
| SKCM | 2 | 152512907 | 152512907 | + | Silent | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr2:152512907G>A | c.6255C>T | c.(6253-6255)ccC>ccT | p.P2085P |
| SKCM | 2 | 152512943 | 152512943 | + | Silent | SNP | C | C | T | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr2:152512943C>T | c.6219G>A | c.(6217-6219)ggG>ggA | p.G2073G |
| SKCM | 2 | 152512943 | 152512943 | + | Silent | SNP | C | C | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr2:152512943C>T | c.6219G>A | c.(6217-6219)ggG>ggA | p.G2073G |
| SKCM | 2 | 152512945 | 152512945 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A199-06A-11D-A197-08 | TCGA-ER-A199-10A-01D-A199-08 | g.chr2:152512945C>T | c.6217G>A | c.(6217-6219)Ggg>Agg | p.G2073R |
| SKCM | 2 | 152514587 | 152514587 | + | Silent | SNP | G | G | A | TCGA-GN-A4U7-06A-21D-A32N-08 | TCGA-GN-A4U7-10B-01D-A32N-08 | g.chr2:152514587G>A | c.6093C>T | c.(6091-6093)tcC>tcT | p.S2031S |
| SKCM | 2 | 152514605 | 152514605 | + | Splice_Site | SNP | C | C | T | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr2:152514605C>T | | c.e48-1 | |
| SKCM | 2 | 152515621 | 152515621 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZC-06A-11D-A197-08 | TCGA-FS-A1ZC-10A-01D-A199-08 | g.chr2:152515621G>A | c.6033C>T | c.(6031-6033)ccC>ccT | p.P2011P |
| SKCM | 2 | 152515623 | 152515623 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152515623G>A | c.6031C>T | c.(6031-6033)Ccc>Tcc | p.P2011S |
| SKCM | 2 | 152515633 | 152515633 | + | Missense_Mutation | SNP | C | C | A | TCGA-FS-A1ZP-06A-11D-A197-08 | TCGA-FS-A1ZP-10A-01D-A199-08 | g.chr2:152515633C>A | c.6021G>T | c.(6019-6021)atG>atT | p.M2007I |
| SKCM | 2 | 152518823 | 152518823 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152518823C>T | c.5796G>A | c.(5794-5796)atG>atA | p.M1932I |
| SKCM | 2 | 152520064 | 152520064 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1QB-06A-11D-A19A-08 | TCGA-D3-A1QB-10A-01D-A19A-08 | g.chr2:152520064C>T | c.5761G>A | c.(5761-5763)Gat>Aat | p.D1921N |
| SKCM | 2 | 152520169 | 152520169 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AF-06A-11D-A196-08 | TCGA-EE-A3AF-10A-01D-A198-08 | g.chr2:152520169C>T | c.5656G>A | c.(5656-5658)Gaa>Aaa | p.E1886K |
| SKCM | 2 | 152520238 | 152520238 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:152520238C>T | c.5587G>A | c.(5587-5589)Gag>Aag | p.E1863K |
| SKCM | 2 | 152520287 | 152520287 | + | Silent | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr2:152520287G>A | c.5538C>T | c.(5536-5538)ttC>ttT | p.F1846F |
| SKCM | 2 | 152520314 | 152520314 | + | Silent | SNP | C | C | T | TCGA-EE-A2GP-06A-11D-A197-08 | TCGA-EE-A2GP-10A-01D-A199-08 | g.chr2:152520314C>T | c.5511G>A | c.(5509-5511)ctG>ctA | p.L1837L |
| SKCM | 2 | 152520314 | 152520314 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152520314C>T | c.5511G>A | c.(5509-5511)ctG>ctA | p.L1837L |
| SKCM | 2 | 152521954 | 152521954 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1I8-06A-11D-A197-08 | TCGA-DA-A1I8-10A-01D-A199-08 | g.chr2:152521954G>A | c.5131C>T | c.(5131-5133)Ctt>Ttt | p.L1711F |
| SKCM | 2 | 152521994 | 152521994 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152521994C>T | c.5091G>A | c.(5089-5091)gaG>gaA | p.E1697E |
| SKCM | 2 | 152522714 | 152522714 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr2:152522714G>A | c.4921C>T | c.(4921-4923)Cag>Tag | p.Q1641* |
| SKCM | 2 | 152522747 | 152522747 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr2:152522747C>T | c.4888G>A | c.(4888-4890)Gat>Aat | p.D1630N |
| SKCM | 2 | 152522759 | 152522759 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr2:152522759G>A | c.4876C>T | c.(4876-4878)Cac>Tac | p.H1626Y |
| SKCM | 2 | 152522801 | 152522801 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr2:152522801G>A | c.4834C>T | c.(4834-4836)Cgt>Tgt | p.R1612C |
| SKCM | 2 | 152524385 | 152524385 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152524385C>T | c.4652G>A | c.(4651-4653)gGc>gAc | p.G1551D |
| SKCM | 2 | 152525626 | 152525626 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZD-06A-11D-A197-08 | TCGA-FS-A1ZD-10A-01D-A199-08 | g.chr2:152525626C>T | c.4526G>A | c.(4525-4527)gGa>gAa | p.G1509E |
| SKCM | 2 | 152527573 | 152527573 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr2:152527573C>T | c.4470G>A | c.(4468-4470)atG>atA | p.M1490I |
| SKCM | 2 | 152527582 | 152527582 | + | Silent | SNP | G | G | A | TCGA-ER-A19M-06A-61D-A23B-08 | TCGA-ER-A19M-10A-01D-A23B-08 | g.chr2:152527582G>A | c.4461C>T | c.(4459-4461)tcC>tcT | p.S1487S |
| SKCM | 2 | 152527697 | 152527697 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152527697C>T | c.4346G>A | c.(4345-4347)tGg>tAg | p.W1449* |
| SKCM | 2 | 152528985 | 152528985 | + | Silent | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr2:152528985G>A | c.4197C>T | c.(4195-4197)gtC>gtT | p.V1399V |
| SKCM | 2 | 152529052 | 152529052 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GB-06A-11D-A197-08 | TCGA-EE-A2GB-10A-01D-A199-08 | g.chr2:152529052G>A | c.4130C>T | c.(4129-4131)aCc>aTc | p.T1377I |
| SKCM | 2 | 152529135 | 152529135 | + | Silent | SNP | G | G | A | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr2:152529135G>A | c.4047C>T | c.(4045-4047)ctC>ctT | p.L1349L |
| SKCM | 2 | 152531836 | 152531836 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-11A-11D-A23B-08 | g.chr2:152531836G>A | c.3844C>T | c.(3844-3846)Ctc>Ttc | p.L1282F |
| SKCM | 2 | 152534098 | 152534098 | + | Missense_Mutation | SNP | T | T | A | TCGA-FR-A3YO-06A-11D-A23B-08 | TCGA-FR-A3YO-10A-01D-A23B-08 | g.chr2:152534098T>A | c.3755A>T | c.(3754-3756)aAc>aTc | p.N1252I |
| SKCM | 2 | 152534195 | 152534195 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr2:152534195C>T | c.3658G>A | c.(3658-3660)Ggt>Agt | p.G1220S |
| SKCM | 2 | 152534213 | 152534213 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr2:152534213C>T | c.3640G>A | c.(3640-3642)Gaa>Aaa | p.E1214K |
| SKCM | 2 | 152534253 | 152534253 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152534253C>T | c.3600G>A | c.(3598-3600)atG>atA | p.M1200I |
| SKCM | 2 | 152534256 | 152534256 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A2GB-06A-11D-A197-08 | TCGA-EE-A2GB-10A-01D-A199-08 | g.chr2:152534256C>T | c.3597G>A | c.(3595-3597)tgG>tgA | p.W1199* |
| SKCM | 2 | 152534274 | 152534274 | + | Silent | SNP | C | C | T | TCGA-EE-A2GL-06A-11D-A196-08 | TCGA-EE-A2GL-10A-01D-A198-08 | g.chr2:152534274C>T | c.3579G>A | c.(3577-3579)aaG>aaA | p.K1193K |
| SKCM | 2 | 152534436 | 152534436 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51E-06A-11D-A25O-08 | TCGA-D3-A51E-10A-01D-A25O-08 | g.chr2:152534436G>A | c.3521C>T | c.(3520-3522)gCc>gTc | p.A1174V |
| SKCM | 2 | 152534673 | 152534673 | + | Missense_Mutation | SNP | G | G | C | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr2:152534673G>C | c.3284C>G | c.(3283-3285)gCt>gGt | p.A1095G |
| SKCM | 2 | 152536512 | 152536512 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GM-06B-11D-A196-08 | TCGA-EE-A2GM-10A-01D-A198-08 | g.chr2:152536512C>T | c.3067G>A | c.(3067-3069)Gaa>Aaa | p.E1023K |
| SKCM | 2 | 152537302 | 152537302 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr2:152537302G>A | c.2984C>T | c.(2983-2985)tCg>tTg | p.S995L |
| SKCM | 2 | 152541387 | 152541387 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr2:152541387C>T | c.2740G>A | c.(2740-2742)Gac>Aac | p.D914N |
| SKCM | 2 | 152541388 | 152541388 | + | Silent | SNP | G | G | A | TCGA-GF-A3OT-06A-23D-A23B-08 | TCGA-GF-A3OT-10A-01D-A23B-08 | g.chr2:152541388G>A | c.2739C>T | c.(2737-2739)agC>agT | p.S913S |
| SKCM | 2 | 152544005 | 152544005 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152544005C>T | c.2565G>A | c.(2563-2565)atG>atA | p.M855I |
| SKCM | 2 | 152544142 | 152544142 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29N-06A-12D-A197-08 | TCGA-EE-A29N-10A-01D-A199-08 | g.chr2:152544142C>T | c.2521G>A | c.(2521-2523)Gat>Aat | p.D841N |
| SKCM | 2 | 152544864 | 152544864 | + | Missense_Mutation | SNP | A | A | G | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:152544864A>G | c.2357T>C | c.(2356-2358)aTa>aCa | p.I786T |
| SKCM | 2 | 152548448 | 152548448 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr2:152548448C>T | c.2141G>A | c.(2140-2142)gGa>gAa | p.G714E |
| SKCM | 2 | 152548668 | 152548668 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr2:152548668C>T | c.2011G>A | c.(2011-2013)Gac>Aac | p.D671N |
| SKCM | 2 | 152550864 | 152550864 | + | Silent | SNP | G | G | A | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr2:152550864G>A | c.1869C>T | c.(1867-1869)tcC>tcT | p.S623S |
| SKCM | 2 | 152550884 | 152550884 | + | Missense_Mutation | SNP | C | C | T | TCGA-RP-A694-06A-11D-A30X-08 | TCGA-RP-A694-10A-01D-A30X-08 | g.chr2:152550884C>T | c.1849G>A | c.(1849-1851)Gat>Aat | p.D617N |
| SKCM | 2 | 152550915 | 152550915 | + | Silent | SNP | C | C | T | TCGA-EE-A2MT-06A-11D-A197-08 | TCGA-EE-A2MT-10A-01D-A199-08 | g.chr2:152550915C>T | c.1818G>A | c.(1816-1818)ggG>ggA | p.G606G |
| SKCM | 2 | 152553214 | 152553214 | + | Silent | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:152553214G>A | c.1506C>T | c.(1504-1506)ttC>ttT | p.F502F |
| SKCM | 2 | 152553713 | 152553713 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152553713C>T | c.1419G>A | c.(1417-1419)caG>caA | p.Q473Q |
| SKCM | 2 | 152553955 | 152553955 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr2:152553955G>A | c.1274C>T | c.(1273-1275)tCc>tTc | p.S425F |
| SKCM | 2 | 152554067 | 152554067 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr2:152554067G>A | c.1248C>T | c.(1246-1248)ttC>ttT | p.F416F |
| SKCM | 2 | 152554087 | 152554087 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr2:152554087C>T | c.1228G>A | c.(1228-1230)Gat>Aat | p.D410N |
| SKCM | 2 | 152554150 | 152554150 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A3Z3-06A-11D-A23B-08 | TCGA-D9-A3Z3-10A-01D-A23B-08 | g.chr2:152554150C>T | c.1165G>A | c.(1165-1167)Gaa>Aaa | p.E389K |
| SKCM | 2 | 152566275 | 152566275 | + | Silent | SNP | C | C | T | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr2:152566275C>T | c.930G>A | c.(928-930)agG>agA | p.R310R |
| SKCM | 2 | 152579986 | 152579986 | + | Silent | SNP | T | T | C | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr2:152579986T>C | c.627A>G | c.(625-627)gaA>gaG | p.E209E |
| SKCM | 2 | 152582002 | 152582002 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51E-06A-11D-A25O-08 | TCGA-D3-A51E-10A-01D-A25O-08 | g.chr2:152582002G>A | c.367C>T | c.(367-369)Cgc>Tgc | p.R123C |
| SKCM | 2 | 152584256 | 152584256 | + | Silent | SNP | G | G | A | TCGA-D3-A51J-06A-11D-A25O-08 | TCGA-D3-A51J-10A-01D-A25O-08 | g.chr2:152584256G>A | c.243C>T | c.(241-243)ttC>ttT | p.F81F |