| 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 | 109380404 | 109380404 | + | Missense_Mutation | SNP | C | C | T | TCGA-OR-A5K9-01A-11D-A29I-10 | TCGA-OR-A5K9-11A-11D-A29L-10 | g.chr2:109380404C>T | c.3409C>T | c.(3409-3411)Cca>Tca | p.P1137S |
| ACC | 2 | 109382319 | 109382319 | + | Missense_Mutation | SNP | T | T | A | TCGA-OR-A5LP-01A-11D-A29I-10 | TCGA-OR-A5LP-10A-01D-A29L-10 | g.chr2:109382319T>A | c.5324T>A | c.(5323-5325)tTt>tAt | p.F1775Y |
| ACC | 2 | 109384075 | 109384075 | + | Missense_Mutation | SNP | A | A | C | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr2:109384075A>C | c.7080A>C | c.(7078-7080)ttA>ttC | p.L2360F |
| BLCA | 2 | 109336129 | 109336129 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-XF-AAN2-01A-11D-A42E-08 | TCGA-XF-AAN2-10A-01D-A42H-08 | g.chr2:109336129C>T | c.67C>T | c.(67-69)Cga>Tga | p.R23* |
| BLCA | 2 | 109347256 | 109347256 | + | Missense_Mutation | SNP | A | A | G | TCGA-ZF-A9RC-01A-11D-A38G-08 | TCGA-ZF-A9RC-10A-01D-A38J-08 | g.chr2:109347256A>G | c.167A>G | c.(166-168)cAa>cGa | p.Q56R |
| BLCA | 2 | 109347808 | 109347808 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9SP-01A-11D-A391-08 | TCGA-XF-A9SP-10A-01D-A394-08 | g.chr2:109347808G>A | c.283G>A | c.(283-285)Gat>Aat | p.D95N |
| BLCA | 2 | 109352069 | 109352069 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr2:109352069G>C | c.487G>C | c.(487-489)Gat>Cat | p.D163H |
| BLCA | 2 | 109356991 | 109356991 | + | Missense_Mutation | SNP | G | G | C | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr2:109356991G>C | c.829G>C | c.(829-831)Gaa>Caa | p.E277Q |
| BLCA | 2 | 109365525 | 109365525 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9RL-01A-11D-A38G-08 | TCGA-ZF-A9RL-10A-01D-A38J-08 | g.chr2:109365525G>C | c.1213G>C | c.(1213-1215)Gat>Cat | p.D405H |
| BLCA | 2 | 109369565 | 109369565 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A3SN-01A-12D-A22Z-08 | TCGA-FD-A3SN-10A-01D-A22Z-08 | g.chr2:109369565C>T | c.1867C>T | c.(1867-1869)Cct>Tct | p.P623S |
| BLCA | 2 | 109374920 | 109374920 | + | Missense_Mutation | SNP | C | C | T | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr2:109374920C>T | c.2518C>T | c.(2518-2520)Cgt>Tgt | p.R840C |
| BLCA | 2 | 109378569 | 109378569 | + | Missense_Mutation | SNP | G | G | C | TCGA-GU-A767-01A-11D-A32B-08 | TCGA-GU-A767-10A-01D-A329-08 | g.chr2:109378569G>C | c.2615G>C | c.(2614-2616)gGc>gCc | p.G872A |
| BLCA | 2 | 109379691 | 109379691 | + | Splice_Site | SNP | A | A | G | TCGA-GV-A3QG-01A-11D-A21Z-08 | TCGA-GV-A3QG-10A-01D-A21Z-08 | g.chr2:109379691A>G | | c.e20-1 | |
| BLCA | 2 | 109380185 | 109380185 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A2LA-01A-11D-A18F-08 | TCGA-BT-A2LA-11A-11D-A18F-08 | g.chr2:109380185G>A | c.3190G>A | c.(3190-3192)Gaa>Aaa | p.E1064K |
| BLCA | 2 | 109380497 | 109380497 | + | Missense_Mutation | SNP | G | G | T | TCGA-FD-A3N5-01A-11D-A21A-08 | TCGA-FD-A3N5-10A-01D-A21A-08 | g.chr2:109380497G>T | c.3502G>T | c.(3502-3504)Gac>Tac | p.D1168Y |
| BLCA | 2 | 109381406 | 109381406 | + | Missense_Mutation | SNP | G | G | T | TCGA-4Z-AA7R-01A-11D-A391-08 | TCGA-4Z-AA7R-10A-01D-A394-08 | g.chr2:109381406G>T | c.4411G>T | c.(4411-4413)Gat>Tat | p.D1471Y |
| BLCA | 2 | 109381658 | 109381658 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-E7-A4XJ-01A-11D-A26M-08 | TCGA-E7-A4XJ-10A-01D-A26K-08 | g.chr2:109381658C>T | c.4663C>T | c.(4663-4665)Cga>Tga | p.R1555* |
| BLCA | 2 | 109381763 | 109381763 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A3WW-01A-22D-A23M-08 | TCGA-DK-A3WW-10A-01D-A23K-08 | g.chr2:109381763G>A | c.4768G>A | c.(4768-4770)Gag>Aag | p.E1590K |
| BLCA | 2 | 109382168 | 109382168 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9T6-01A-11D-A42E-08 | TCGA-XF-A9T6-10A-01D-A42H-08 | g.chr2:109382168G>A | c.5173G>A | c.(5173-5175)Gaa>Aaa | p.E1725K |
| BLCA | 2 | 109382445 | 109382445 | + | Missense_Mutation | SNP | C | C | T | TCGA-E5-A2PC-01A-11D-A202-08 | TCGA-E5-A2PC-10B-01D-A202-08 | g.chr2:109382445C>T | c.5450C>T | c.(5449-5451)gCt>gTt | p.A1817V |
| BLCA | 2 | 109382490 | 109382490 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr2:109382490C>T | c.5495C>T | c.(5494-5496)tCt>tTt | p.S1832F |
| BLCA | 2 | 109382741 | 109382741 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9SJ-01A-11D-A391-08 | TCGA-XF-A9SJ-10A-01D-A394-08 | g.chr2:109382741C>G | c.5746C>G | c.(5746-5748)Ctt>Gtt | p.L1916V |
| BLCA | 2 | 109383083 | 109383083 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr2:109383083G>A | c.6088G>A | c.(6088-6090)Gaa>Aaa | p.E2030K |
| BLCA | 2 | 109383109 | 109383109 | + | Silent | SNP | G | G | A | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr2:109383109G>A | c.6114G>A | c.(6112-6114)caG>caA | p.Q2038Q |
| BLCA | 2 | 109383113 | 109383113 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A7PW-01A-11D-A34U-08 | TCGA-E7-A7PW-10A-01D-A34X-08 | g.chr2:109383113G>A | c.6118G>A | c.(6118-6120)Gta>Ata | p.V2040I |
| BLCA | 2 | 109383783 | 109383783 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-DK-A3IT-01A-31D-A20D-08 | TCGA-DK-A3IT-10A-01D-A20D-08 | g.chr2:109383783C>G | c.6788C>G | c.(6787-6789)tCa>tGa | p.S2263* |
| BLCA | 2 | 109384287 | 109384287 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A6TK-01A-42D-A339-08 | TCGA-FD-A6TK-10A-21D-A339-08 | g.chr2:109384287C>T | c.7292C>T | c.(7291-7293)tCg>tTg | p.S2431L |
| BLCA | 2 | 109384816 | 109384816 | + | Missense_Mutation | SNP | C | C | G | TCGA-GD-A2C5-01A-12D-A17V-08 | TCGA-GD-A2C5-10A-01D-A17V-08 | g.chr2:109384816C>G | c.7821C>G | c.(7819-7821)atC>atG | p.I2607M |
| BLCA | 2 | 109388219 | 109388219 | + | Silent | SNP | C | C | T | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr2:109388219C>T | c.7912C>T | c.(7912-7914)Cta>Tta | p.L2638L |
| BLCA | 2 | 109389434 | 109389434 | + | Missense_Mutation | SNP | G | G | C | TCGA-K4-A5RJ-01A-11D-A289-08 | TCGA-K4-A5RJ-10A-01D-A289-08 | g.chr2:109389434G>C | c.8224G>C | c.(8224-8226)Gat>Cat | p.D2742H |
| BLCA | 2 | 109392268 | 109392268 | + | Silent | SNP | T | T | C | TCGA-XF-A9T0-01A-11D-A391-08 | TCGA-XF-A9T0-10A-01D-A394-08 | g.chr2:109392268T>C | c.8373T>C | c.(8371-8373)tgT>tgC | p.C2791C |
| BLCA | 2 | 109393588 | 109393588 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-AAML-01A-11D-A42E-08 | TCGA-XF-AAML-10A-01D-A42H-08 | g.chr2:109393588G>A | c.8500G>A | c.(8500-8502)Gaa>Aaa | p.E2834K |
| BLCA | 2 | 109398587 | 109398587 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A1A3-01A-11D-A13W-08 | TCGA-DK-A1A3-10A-01D-A13W-08 | g.chr2:109398587G>A | c.8764G>A | c.(8764-8766)Gaa>Aaa | p.E2922K |
| BLCA | 2 | 109398640 | 109398640 | + | Silent | SNP | A | A | G | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr2:109398640A>G | c.8817A>G | c.(8815-8817)aaA>aaG | p.K2939K |
| BLCA | 2 | 109400167 | 109400167 | + | Missense_Mutation | SNP | A | A | G | TCGA-FD-A3SP-01A-31D-A22Z-08 | TCGA-FD-A3SP-10A-01D-A22Z-08 | g.chr2:109400167A>G | c.9485A>G | c.(9484-9486)aAt>aGt | p.N3162S |
| BRCA | 2 | 109347330 | 109347330 | + | Missense_Mutation | SNP | G | G | A | TCGA-E9-A1NF-01A-11D-A14G-09 | TCGA-E9-A1NF-10A-01D-A14G-09 | g.chr2:109347330G>A | c.241G>A | c.(241-243)Gaa>Aaa | p.E81K |
| BRCA | 2 | 109367878 | 109367878 | + | Missense_Mutation | SNP | T | T | G | TCGA-E9-A1N8-01A-11D-A142-09 | TCGA-E9-A1N8-10A-01D-A142-09 | g.chr2:109367878T>G | c.1432T>G | c.(1432-1434)Tca>Gca | p.S478A |
| BRCA | 2 | 109368406 | 109368406 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr2:109368406C>T | c.1711C>T | c.(1711-1713)Caa>Taa | p.Q571* |
| BRCA | 2 | 109371670 | 109371670 | + | Missense_Mutation | SNP | G | G | C | TCGA-A2-A0EQ-01A-11W-A050-09 | TCGA-A2-A0EQ-10A-01W-A055-09 | g.chr2:109371670G>C | c.2421G>C | c.(2419-2421)caG>caC | p.Q807H |
| BRCA | 2 | 109380048 | 109380048 | + | Missense_Mutation | SNP | C | C | G | TCGA-EW-A1OV-01A-11D-A142-09 | TCGA-EW-A1OV-10A-01D-A142-09 | g.chr2:109380048C>G | c.3053C>G | c.(3052-3054)tCt>tGt | p.S1018C |
| BRCA | 2 | 109380099 | 109380099 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-AR-A0TX-01A-11D-A099-09 | TCGA-AR-A0TX-10A-01D-A099-09 | g.chr2:109380099C>G | c.3104C>G | c.(3103-3105)tCa>tGa | p.S1035* |
| BRCA | 2 | 109380159 | 109380160 | + | Missense_Mutation | DNP | CC | CC | TA | TCGA-AR-A2LR-01A-12D-A18P-09 | TCGA-AR-A2LR-10A-01D-A18P-09 | g.chr2:109380159_109380160CC>TA | c.3164_3165CC>TA | c.(3163-3165)cCC>cTA | p.P1055L |
| BRCA | 2 | 109380363 | 109380363 | + | Missense_Mutation | SNP | C | C | G | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr2:109380363C>G | c.3368C>G | c.(3367-3369)tCt>tGt | p.S1123C |
| BRCA | 2 | 109380485 | 109380487 | + | In_Frame_Del | DEL | GAT | GAT | - | TCGA-AR-A255-01A-11D-A167-09 | TCGA-AR-A255-10A-01D-A167-09 | g.chr2:109380485_109380487delGAT | c.3490_3492delGAT | c.(3490-3492)gatdel | p.D1168del |
| BRCA | 2 | 109381005 | 109381005 | + | Missense_Mutation | SNP | C | C | G | TCGA-GM-A2D9-01A-11D-A18P-09 | TCGA-GM-A2D9-11A-42D-A18P-09 | g.chr2:109381005C>G | c.4010C>G | c.(4009-4011)tCt>tGt | p.S1337C |
| BRCA | 2 | 109381329 | 109381329 | + | Missense_Mutation | SNP | A | A | G | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr2:109381329A>G | c.4334A>G | c.(4333-4335)aAc>aGc | p.N1445S |
| BRCA | 2 | 109384012 | 109384012 | + | Silent | SNP | C | C | G | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr2:109384012C>G | c.7017C>G | c.(7015-7017)ctC>ctG | p.L2339L |
| BRCA | 2 | 109384566 | 109384566 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AN-A0AK-01A-21W-A019-09 | TCGA-AN-A0AK-10A-01W-A021-09 | g.chr2:109384566delT | c.7571delT | c.(7570-7572)attfs | p.I2524fs |
| BRCA | 2 | 109388956 | 109388956 | + | Missense_Mutation | SNP | G | G | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr2:109388956G>A | c.8032G>A | c.(8032-8034)Gaa>Aaa | p.E2678K |
| BRCA | 2 | 109389434 | 109389434 | + | Missense_Mutation | SNP | G | G | A | TCGA-EW-A1J5-01A-11D-A13L-09 | TCGA-EW-A1J5-10A-01D-A13O-09 | g.chr2:109389434G>A | c.8224G>A | c.(8224-8226)Gat>Aat | p.D2742N |
| CESC | 2 | 109345596 | 109345596 | + | Missense_Mutation | SNP | G | G | T | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr2:109345596G>T | c.81G>T | c.(79-81)atG>atT | p.M27I |
| CESC | 2 | 109347309 | 109347309 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A1BF-01B-11D-A13W-08 | TCGA-C5-A1BF-10A-01D-A13W-08 | g.chr2:109347309G>A | c.220G>A | c.(220-222)Gaa>Aaa | p.E74K |
| CESC | 2 | 109380099 | 109380099 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-Q1-A5R2-01A-11D-A28B-09 | TCGA-Q1-A5R2-10A-01D-A28E-09 | g.chr2:109380099C>G | c.3104C>G | c.(3103-3105)tCa>tGa | p.S1035* |
| CESC | 2 | 109381095 | 109381095 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr2:109381095C>T | c.4100C>T | c.(4099-4101)tCa>tTa | p.S1367L |
| CESC | 2 | 109381352 | 109381352 | + | Missense_Mutation | SNP | C | C | T | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr2:109381352C>T | c.4357C>T | c.(4357-4359)Cat>Tat | p.H1453Y |
| CESC | 2 | 109383853 | 109383853 | + | Missense_Mutation | SNP | G | G | C | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr2:109383853G>C | c.6858G>C | c.(6856-6858)caG>caC | p.Q2286H |
| CHOL | 2 | 109379749 | 109379749 | + | Silent | SNP | G | G | A | TCGA-ZU-A8S4-01A-11D-A417-09 | TCGA-ZU-A8S4-10A-01D-A41A-09 | g.chr2:109379749G>A | c.2754G>A | c.(2752-2754)ccG>ccA | p.P918P |
| COAD | 2 | 109347840 | 109347841 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr2:109347840_109347841insA | c.315_316insA | c.(316-318)aaafs | p.K106fs |
| COAD | 2 | 109352635 | 109352635 | + | Missense_Mutation | SNP | G | G | T | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr2:109352635G>T | c.712G>T | c.(712-714)Gcc>Tcc | p.A238S |
| COAD | 2 | 109352677 | 109352677 | + | Missense_Mutation | SNP | G | G | T | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr2:109352677G>T | c.754G>T | c.(754-756)Gtg>Ttg | p.V252L |
| COAD | 2 | 109368070 | 109368070 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3680-01A-01W-0900-09 | TCGA-AA-3680-10A-01W-0900-09 | g.chr2:109368070C>A | c.1542C>A | c.(1540-1542)tgC>tgA | p.C514* |
| COAD | 2 | 109368357 | 109368357 | + | Silent | SNP | A | A | G | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:109368357A>G | c.1662A>G | c.(1660-1662)ctA>ctG | p.L554L |
| COAD | 2 | 109379847 | 109379847 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3526-01A-02W-0831-10 | TCGA-AA-3526-10A-01W-0831-10 | g.chr2:109379847C>T | c.2852C>T | c.(2851-2853)aCg>aTg | p.T951M |
| COAD | 2 | 109379946 | 109379946 | + | Missense_Mutation | SNP | C | C | A | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr2:109379946C>A | c.2951C>A | c.(2950-2952)cCt>cAt | p.P984H |
| COAD | 2 | 109380297 | 109380297 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A28G-01A-11D-A16V-10 | TCGA-DM-A28G-10A-01D-A16V-10 | g.chr2:109380297T>C | c.3302T>C | c.(3301-3303)tTt>tCt | p.F1101S |
| COAD | 2 | 109380516 | 109380516 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr2:109380516C>T | c.3521C>T | c.(3520-3522)cCt>cTt | p.P1174L |
| COAD | 2 | 109380592 | 109380592 | + | Silent | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:109380592G>A | c.3597G>A | c.(3595-3597)gcG>gcA | p.A1199A |
| COAD | 2 | 109380602 | 109380602 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr2:109380602C>T | c.3607C>T | c.(3607-3609)Cgt>Tgt | p.R1203C |
| COAD | 2 | 109380686 | 109380686 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:109380686C>T | c.3691C>T | c.(3691-3693)Cgc>Tgc | p.R1231C |
| COAD | 2 | 109380720 | 109380720 | + | Missense_Mutation | SNP | T | T | G | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr2:109380720T>G | c.3725T>G | c.(3724-3726)aTc>aGc | p.I1242S |
| COAD | 2 | 109380968 | 109380968 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:109380968G>T | c.3973G>T | c.(3973-3975)Gaa>Taa | p.E1325* |
| COAD | 2 | 109381259 | 109381259 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr2:109381259A>G | c.4264A>G | c.(4264-4266)Agt>Ggt | p.S1422G |
| COAD | 2 | 109381730 | 109381730 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:109381730C>A | c.4735C>A | c.(4735-4737)Cca>Aca | p.P1579T |
| COAD | 2 | 109382689 | 109382689 | + | Silent | SNP | T | T | C | TCGA-AA-3980-01A-02W-0995-10 | TCGA-AA-3980-10A-01W-0999-10 | g.chr2:109382689T>C | c.5694T>C | c.(5692-5694)ttT>ttC | p.F1898F |
| COAD | 2 | 109383653 | 109383653 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr2:109383653C>T | c.6658C>T | c.(6658-6660)Ccc>Tcc | p.P2220S |
| COAD | 2 | 109383756 | 109383757 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AA-A02J-01A-01W-A00E-09 | TCGA-AA-A02J-10A-01W-A00E-09 | g.chr2:109383756_109383757insA | c.6761_6762insA | c.(6760-6765)agaaaafs | p.RK2254fs |
| COAD | 2 | 109384188 | 109384188 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:109384188C>T | c.7193C>T | c.(7192-7194)aCa>aTa | p.T2398I |
| COAD | 2 | 109384718 | 109384718 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr2:109384718delA | c.7723delA | c.(7723-7725)aaafs | p.K2576fs |
| COAD | 2 | 109384779 | 109384779 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:109384779A>C | c.7784A>C | c.(7783-7785)aAt>aCt | p.N2595T |
| COAD | 2 | 109389335 | 109389335 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr2:109389335G>T | c.8125G>T | c.(8125-8127)Gaa>Taa | p.E2709* |
| COAD | 2 | 109389413 | 109389413 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr2:109389413delT | c.8203delT | c.(8203-8205)tttfs | p.F2736fs |
| COAD | 2 | 109399069 | 109399069 | + | Missense_Mutation | SNP | T | T | G | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr2:109399069T>G | c.9120T>G | c.(9118-9120)tgT>tgG | p.C3040W |
| COAD | 2 | 109399172 | 109399172 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr2:109399172G>A | c.9223G>A | c.(9223-9225)Gaa>Aaa | p.E3075K |
| COAD | 2 | 109399283 | 109399284 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr2:109399283_109399284insT | c.9334_9335insT | c.(9334-9336)attfs | p.I3112fs |
| COADREAD | 2 | 109347840 | 109347841 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr2:109347840_109347841insA | c.315_316insA | c.(316-318)aaafs | p.K106fs |
| COADREAD | 2 | 109352028 | 109352028 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr2:109352028A>C | c.446A>C | c.(445-447)aAa>aCa | p.K149T |
| COADREAD | 2 | 109352635 | 109352635 | + | Missense_Mutation | SNP | G | G | T | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr2:109352635G>T | c.712G>T | c.(712-714)Gcc>Tcc | p.A238S |
| COADREAD | 2 | 109352677 | 109352677 | + | Missense_Mutation | SNP | G | G | T | TCGA-CM-4744-01A-01D-1408-10 | TCGA-CM-4744-10A-01D-1408-10 | g.chr2:109352677G>T | c.754G>T | c.(754-756)Gtg>Ttg | p.V252L |
| COADREAD | 2 | 109368070 | 109368070 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3680-01A-01W-0900-09 | TCGA-AA-3680-10A-01W-0900-09 | g.chr2:109368070C>A | c.1542C>A | c.(1540-1542)tgC>tgA | p.C514* |
| COADREAD | 2 | 109368357 | 109368357 | + | Silent | SNP | A | A | G | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:109368357A>G | c.1662A>G | c.(1660-1662)ctA>ctG | p.L554L |
| COADREAD | 2 | 109368375 | 109368375 | + | Silent | SNP | C | C | T | TCGA-F5-6813-01A-11D-1826-10 | TCGA-F5-6813-10A-01D-1826-10 | g.chr2:109368375C>T | c.1680C>T | c.(1678-1680)aaC>aaT | p.N560N |
| COADREAD | 2 | 109369470 | 109369470 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109369470C>A | c.1772C>A | c.(1771-1773)tCt>tAt | p.S591Y |
| COADREAD | 2 | 109379749 | 109379749 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109379749G>A | c.2754G>A | c.(2752-2754)ccG>ccA | p.P918P |
| COADREAD | 2 | 109379847 | 109379847 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3526-01A-02W-0831-10 | TCGA-AA-3526-10A-01W-0831-10 | g.chr2:109379847C>T | c.2852C>T | c.(2851-2853)aCg>aTg | p.T951M |
| COADREAD | 2 | 109379946 | 109379946 | + | Missense_Mutation | SNP | C | C | A | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr2:109379946C>A | c.2951C>A | c.(2950-2952)cCt>cAt | p.P984H |
| COADREAD | 2 | 109380297 | 109380297 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A28G-01A-11D-A16V-10 | TCGA-DM-A28G-10A-01D-A16V-10 | g.chr2:109380297T>C | c.3302T>C | c.(3301-3303)tTt>tCt | p.F1101S |
| COADREAD | 2 | 109380516 | 109380516 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr2:109380516C>T | c.3521C>T | c.(3520-3522)cCt>cTt | p.P1174L |
| COADREAD | 2 | 109380592 | 109380592 | + | Silent | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr2:109380592G>A | c.3597G>A | c.(3595-3597)gcG>gcA | p.A1199A |
| COADREAD | 2 | 109380602 | 109380602 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr2:109380602C>T | c.3607C>T | c.(3607-3609)Cgt>Tgt | p.R1203C |
| COADREAD | 2 | 109380686 | 109380686 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr2:109380686C>T | c.3691C>T | c.(3691-3693)Cgc>Tgc | p.R1231C |
| COADREAD | 2 | 109380686 | 109380686 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109380686C>T | c.3691C>T | c.(3691-3693)Cgc>Tgc | p.R1231C |
| COADREAD | 2 | 109380720 | 109380720 | + | Missense_Mutation | SNP | T | T | G | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr2:109380720T>G | c.3725T>G | c.(3724-3726)aTc>aGc | p.I1242S |
| COADREAD | 2 | 109380930 | 109380930 | + | Missense_Mutation | SNP | T | T | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109380930T>C | c.3935T>C | c.(3934-3936)gTa>gCa | p.V1312A |
| COADREAD | 2 | 109380968 | 109380968 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr2:109380968G>T | c.3973G>T | c.(3973-3975)Gaa>Taa | p.E1325* |
| COADREAD | 2 | 109381259 | 109381259 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr2:109381259A>G | c.4264A>G | c.(4264-4266)Agt>Ggt | p.S1422G |
| COADREAD | 2 | 109381730 | 109381730 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr2:109381730C>A | c.4735C>A | c.(4735-4737)Cca>Aca | p.P1579T |
| COADREAD | 2 | 109382689 | 109382689 | + | Silent | SNP | T | T | C | TCGA-AA-3980-01A-02W-0995-10 | TCGA-AA-3980-10A-01W-0999-10 | g.chr2:109382689T>C | c.5694T>C | c.(5692-5694)ttT>ttC | p.F1898F |
| COADREAD | 2 | 109382902 | 109382902 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109382902G>T | c.5907G>T | c.(5905-5907)aaG>aaT | p.K1969N |
| COADREAD | 2 | 109382974 | 109382974 | + | Silent | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109382974C>T | c.5979C>T | c.(5977-5979)tcC>tcT | p.S1993S |
| COADREAD | 2 | 109383653 | 109383653 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr2:109383653C>T | c.6658C>T | c.(6658-6660)Ccc>Tcc | p.P2220S |
| COADREAD | 2 | 109383756 | 109383757 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AA-A02J-01A-01W-A00E-09 | TCGA-AA-A02J-10A-01W-A00E-09 | g.chr2:109383756_109383757insA | c.6761_6762insA | c.(6760-6765)agaaaafs | p.RK2254fs |
| COADREAD | 2 | 109384117 | 109384117 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr2:109384117G>T | c.7122G>T | c.(7120-7122)agG>agT | p.R2374S |
| COADREAD | 2 | 109384127 | 109384127 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109384127T>G | c.7132T>G | c.(7132-7134)Tta>Gta | p.L2378V |
| COADREAD | 2 | 109384188 | 109384188 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr2:109384188C>T | c.7193C>T | c.(7192-7194)aCa>aTa | p.T2398I |
| COADREAD | 2 | 109384299 | 109384299 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109384299T>G | c.7304T>G | c.(7303-7305)aTt>aGt | p.I2435S |
| COADREAD | 2 | 109384718 | 109384718 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr2:109384718delA | c.7723delA | c.(7723-7725)aaafs | p.K2576fs |
| COADREAD | 2 | 109384779 | 109384779 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr2:109384779A>C | c.7784A>C | c.(7783-7785)aAt>aCt | p.N2595T |
| COADREAD | 2 | 109389335 | 109389335 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr2:109389335G>T | c.8125G>T | c.(8125-8127)Gaa>Taa | p.E2709* |
| COADREAD | 2 | 109389413 | 109389413 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr2:109389413delT | c.8203delT | c.(8203-8205)tttfs | p.F2736fs |
| COADREAD | 2 | 109399069 | 109399069 | + | Missense_Mutation | SNP | T | T | G | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr2:109399069T>G | c.9120T>G | c.(9118-9120)tgT>tgG | p.C3040W |
| COADREAD | 2 | 109399172 | 109399172 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr2:109399172G>A | c.9223G>A | c.(9223-9225)Gaa>Aaa | p.E3075K |
| COADREAD | 2 | 109399283 | 109399284 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr2:109399283_109399284insT | c.9334_9335insT | c.(9334-9336)attfs | p.I3112fs |
| DLBC | 2 | 109347314 | 109347314 | + | Missense_Mutation | SNP | C | C | G | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr2:109347314C>G | c.225C>G | c.(223-225)aaC>aaG | p.N75K |
| DLBC | 2 | 109384665 | 109384665 | + | Missense_Mutation | SNP | A | A | G | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr2:109384665A>G | c.7670A>G | c.(7669-7671)aAt>aGt | p.N2557S |
| DLBC | 2 | 109392255 | 109392255 | + | Missense_Mutation | SNP | T | T | G | TCGA-GS-A9TV-01A-11D-A382-10 | TCGA-GS-A9TV-10A-01D-A385-10 | g.chr2:109392255T>G | c.8360T>G | c.(8359-8361)gTa>gGa | p.V2787G |
| ESCA | 2 | 109347782 | 109347782 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A4A6-01A-11D-A27G-09 | TCGA-LN-A4A6-10A-01D-A27G-09 | g.chr2:109347782C>T | c.257C>T | c.(256-258)tCa>tTa | p.S86L |
| ESCA | 2 | 109367786 | 109367786 | + | Missense_Mutation | SNP | T | T | C | TCGA-L5-A88S-01A-11D-A36J-09 | TCGA-L5-A88S-11A-21D-A36M-09 | g.chr2:109367786T>C | c.1340T>C | c.(1339-1341)tTg>tCg | p.L447S |
| ESCA | 2 | 109368085 | 109368085 | + | Silent | SNP | G | G | A | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr2:109368085G>A | c.1557G>A | c.(1555-1557)gtG>gtA | p.V519V |
| ESCA | 2 | 109371641 | 109371641 | + | Missense_Mutation | SNP | A | A | G | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr2:109371641A>G | c.2392A>G | c.(2392-2394)Aaa>Gaa | p.K798E |
| ESCA | 2 | 109381161 | 109381161 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A49P-01A-11D-A247-09 | TCGA-LN-A49P-10A-01D-A247-09 | g.chr2:109381161C>T | c.4166C>T | c.(4165-4167)cCa>cTa | p.P1389L |
| ESCA | 2 | 109382709 | 109382709 | + | Missense_Mutation | SNP | C | C | T | TCGA-JY-A93E-01A-11D-A37C-09 | TCGA-JY-A93E-10A-01D-A37F-09 | g.chr2:109382709C>T | c.5714C>T | c.(5713-5715)cCa>cTa | p.P1905L |
| ESCA | 2 | 109384333 | 109384333 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-L5-A893-01A-11D-A36J-09 | TCGA-L5-A893-11A-21D-A36M-09 | g.chr2:109384333delT | c.7338delT | c.(7336-7338)gatfs | p.D2446fs |
| GBM | 2 | 109388156 | 109388156 | + | Splice_Site | SNP | G | G | A | TCGA-27-2521-01A-01D-1494-08 | TCGA-27-2521-10A-01D-1494-08 | g.chr2:109388156G>A | | c.e21-1 | |
| GBMLGG | 2 | 109357066 | 109357066 | + | Missense_Mutation | SNP | C | C | A | TCGA-E1-A7Z4-01A-11D-A34J-08 | TCGA-E1-A7Z4-10A-01D-A34M-08 | g.chr2:109357066C>A | c.904C>A | c.(904-906)Cag>Aag | p.Q302K |
| GBMLGG | 2 | 109365547 | 109365547 | + | Missense_Mutation | SNP | G | G | A | TCGA-WH-A86K-01A-11D-A36O-08 | TCGA-WH-A86K-10A-01D-A367-08 | g.chr2:109365547G>A | c.1235G>A | c.(1234-1236)cGa>cAa | p.R412Q |
| GBMLGG | 2 | 109365585 | 109365585 | + | Splice_Site | SNP | G | G | T | TCGA-HT-8012-01A-11D-2395-08 | TCGA-HT-8012-10A-01D-2396-08 | g.chr2:109365585G>T | c.1273G>T | c.(1273-1275)Ggt>Tgt | p.G425C |
| GBMLGG | 2 | 109368336 | 109368336 | + | Silent | SNP | C | C | T | TCGA-TQ-A7RW-01A-11D-A33T-08 | TCGA-TQ-A7RW-10A-01D-A33W-08 | g.chr2:109368336C>T | c.1641C>T | c.(1639-1641)aaC>aaT | p.N547N |
| GBMLGG | 2 | 109368449 | 109368449 | + | Splice_Site | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:109368449C>T | c.1754C>T | c.(1753-1755)aCg>aTg | p.T585M |
| GBMLGG | 2 | 109370354 | 109370354 | + | Missense_Mutation | SNP | A | A | G | TCGA-R8-A73M-01A-11D-A32B-08 | TCGA-R8-A73M-10C-01D-A329-08 | g.chr2:109370354A>G | c.2129A>G | c.(2128-2130)tAt>tGt | p.Y710C |
| GBMLGG | 2 | 109380084 | 109380084 | + | Missense_Mutation | SNP | C | C | A | TCGA-VM-A8CB-01A-11D-A36O-08 | TCGA-VM-A8CB-10A-01D-A367-08 | g.chr2:109380084C>A | c.3089C>A | c.(3088-3090)cCt>cAt | p.P1030H |
| GBMLGG | 2 | 109382889 | 109382889 | + | Missense_Mutation | SNP | A | A | G | TCGA-HT-7687-01A-11D-2253-08 | TCGA-HT-7687-10A-01D-2253-08 | g.chr2:109382889A>G | c.5894A>G | c.(5893-5895)gAc>gGc | p.D1965G |
| GBMLGG | 2 | 109382974 | 109382974 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:109382974C>T | c.5979C>T | c.(5977-5979)tcC>tcT | p.S1993S |
| GBMLGG | 2 | 109383056 | 109383056 | + | Missense_Mutation | SNP | G | G | A | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr2:109383056G>A | c.6061G>A | c.(6061-6063)Gaa>Aaa | p.E2021K |
| GBMLGG | 2 | 109383804 | 109383804 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:109383804G>T | c.6809G>T | c.(6808-6810)aGt>aTt | p.S2270I |
| GBMLGG | 2 | 109384118 | 109384118 | + | Missense_Mutation | SNP | G | G | A | TCGA-P5-A72U-01A-31D-A32B-08 | TCGA-P5-A72U-10A-01D-A329-08 | g.chr2:109384118G>A | c.7123G>A | c.(7123-7125)Gac>Aac | p.D2375N |
| GBMLGG | 2 | 109384409 | 109384409 | + | Missense_Mutation | SNP | T | T | A | TCGA-WY-A85B-01A-11D-A36O-08 | TCGA-WY-A85B-10A-01D-A367-08 | g.chr2:109384409T>A | c.7414T>A | c.(7414-7416)Tta>Ata | p.L2472I |
| GBMLGG | 2 | 109388156 | 109388156 | + | Splice_Site | SNP | G | G | A | TCGA-27-2521-01A-01D-1494-08 | TCGA-27-2521-10A-01D-1494-08 | g.chr2:109388156G>A | | c.e21-1 | |
| GBMLGG | 2 | 109400287 | 109400287 | + | Missense_Mutation | SNP | T | T | C | TCGA-FG-A4MU-01B-11D-A289-08 | TCGA-FG-A4MU-10A-01D-A289-08 | g.chr2:109400287T>C | c.9605T>C | c.(9604-9606)aTt>aCt | p.I3202T |
| HNSC | 2 | 109352601 | 109352601 | + | Silent | SNP | T | T | C | TCGA-CR-7391-01A-11D-2012-08 | TCGA-CR-7391-10A-01D-2013-08 | g.chr2:109352601T>C | c.678T>C | c.(676-678)agT>agC | p.S226S |
| HNSC | 2 | 109357008 | 109357008 | + | Missense_Mutation | SNP | C | C | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr2:109357008C>A | c.846C>A | c.(844-846)ttC>ttA | p.F282L |
| HNSC | 2 | 109357023 | 109357023 | + | Silent | SNP | A | A | T | TCGA-BA-A4IH-01A-11D-A25Y-08 | TCGA-BA-A4IH-10A-01D-A25Y-08 | g.chr2:109357023A>T | c.861A>T | c.(859-861)ggA>ggT | p.G287G |
| HNSC | 2 | 109367719 | 109367719 | + | Splice_Site | SNP | G | G | T | TCGA-CV-5432-01A-02D-1683-08 | TCGA-CV-5432-10A-01D-1870-08 | g.chr2:109367719G>T | | c.e10-1 | |
| HNSC | 2 | 109367852 | 109367852 | + | Missense_Mutation | SNP | C | C | T | TCGA-IQ-A61I-01A-11D-A30E-08 | TCGA-IQ-A61I-10A-01D-A30H-08 | g.chr2:109367852C>T | c.1406C>T | c.(1405-1407)tCa>tTa | p.S469L |
| HNSC | 2 | 109370370 | 109370370 | + | Silent | SNP | G | G | A | TCGA-CN-A6V6-01A-12D-A34J-08 | TCGA-CN-A6V6-10A-01D-A34M-08 | g.chr2:109370370G>A | c.2145G>A | c.(2143-2145)agG>agA | p.R715R |
| HNSC | 2 | 109371714 | 109371714 | + | Splice_Site | SNP | A | A | C | TCGA-CV-A6K1-01A-11D-A31L-08 | TCGA-CV-A6K1-10A-01D-A31J-08 | g.chr2:109371714A>C | c.2465A>C | c.(2464-2466)aAg>aCg | p.K822T |
| HNSC | 2 | 109379847 | 109379847 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-A499-01A-11D-A24D-08 | TCGA-CN-A499-10A-01D-A24F-08 | g.chr2:109379847C>T | c.2852C>T | c.(2851-2853)aCg>aTg | p.T951M |
| HNSC | 2 | 109380846 | 109380846 | + | Missense_Mutation | SNP | G | G | A | TCGA-QK-A8Z9-01B-11D-A391-08 | TCGA-QK-A8Z9-10A-01D-A394-08 | g.chr2:109380846G>A | c.3851G>A | c.(3850-3852)aGg>aAg | p.R1284K |
| HNSC | 2 | 109382140 | 109382140 | + | Silent | SNP | C | C | T | TCGA-CN-6989-01A-11D-1912-08 | TCGA-CN-6989-10A-01D-1912-08 | g.chr2:109382140C>T | c.5145C>T | c.(5143-5145)agC>agT | p.S1715S |
| HNSC | 2 | 109382596 | 109382596 | + | Silent | SNP | A | A | G | TCGA-BA-A4IG-01A-11D-A25Y-08 | TCGA-BA-A4IG-10A-01D-A25Y-08 | g.chr2:109382596A>G | c.5601A>G | c.(5599-5601)gaA>gaG | p.E1867E |
| HNSC | 2 | 109382704 | 109382704 | + | Silent | SNP | G | G | A | TCGA-UF-A7JV-01A-11D-A34J-08 | TCGA-UF-A7JV-10A-01D-A34M-08 | g.chr2:109382704G>A | c.5709G>A | c.(5707-5709)tcG>tcA | p.S1903S |
| HNSC | 2 | 109383191 | 109383191 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-5369-01A-01D-1434-08 | TCGA-CN-5369-10A-01D-1434-08 | g.chr2:109383191G>A | c.6196G>A | c.(6196-6198)Gag>Aag | p.E2066K |
| HNSC | 2 | 109383270 | 109383270 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-6022-01A-21D-1683-08 | TCGA-CN-6022-10A-01D-1683-08 | g.chr2:109383270C>T | c.6275C>T | c.(6274-6276)aCg>aTg | p.T2092M |
| HNSC | 2 | 109383857 | 109383857 | + | Missense_Mutation | SNP | G | G | A | TCGA-MT-A67F-01A-11D-A30E-08 | TCGA-MT-A67F-10A-01D-A30H-08 | g.chr2:109383857G>A | c.6862G>A | c.(6862-6864)Ggg>Agg | p.G2288R |
| HNSC | 2 | 109383938 | 109383938 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-A45Y-01A-11D-A25D-08 | TCGA-CV-A45Y-10A-01D-A25E-08 | g.chr2:109383938C>G | c.6943C>G | c.(6943-6945)Cct>Gct | p.P2315A |
| HNSC | 2 | 109383950 | 109383950 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-6954-01A-11D-1912-08 | TCGA-CV-6954-10A-01D-1912-08 | g.chr2:109383950C>G | c.6955C>G | c.(6955-6957)Cta>Gta | p.L2319V |
| HNSC | 2 | 109392196 | 109392196 | + | Missense_Mutation | SNP | G | G | C | TCGA-CV-7424-01A-11D-2078-08 | TCGA-CV-7424-10A-01D-2078-08 | g.chr2:109392196G>C | c.8301G>C | c.(8299-8301)caG>caC | p.Q2767H |
| HNSC | 2 | 109398721 | 109398721 | + | Silent | SNP | G | G | A | TCGA-TN-A7HL-01A-11D-A34J-08 | TCGA-TN-A7HL-10A-01D-A34M-08 | g.chr2:109398721G>A | c.8898G>A | c.(8896-8898)aaG>aaA | p.K2966K |
| HNSC | 2 | 109399034 | 109399034 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr2:109399034G>T | c.9085G>T | c.(9085-9087)Gta>Tta | p.V3029L |
| HNSC | 2 | 109399112 | 109399112 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-5327-01A-01D-1683-08 | TCGA-CQ-5327-10A-01D-1683-08 | g.chr2:109399112G>A | c.9163G>A | c.(9163-9165)Gca>Aca | p.A3055T |
| HNSC | 2 | 109399178 | 109399178 | + | Silent | SNP | C | C | T | TCGA-CQ-5333-01A-01D-2394-08 | TCGA-CQ-5333-10A-01D-2394-08 | g.chr2:109399178C>T | c.9229C>T | c.(9229-9231)Cta>Tta | p.L3077L |
| KICH | 2 | 109383357 | 109383357 | + | Missense_Mutation | SNP | A | A | G | TCGA-KL-8341-01A-11D-2310-10 | TCGA-KL-8341-11A-01D-2310-10 | g.chr2:109383357A>G | c.6362A>G | c.(6361-6363)cAg>cGg | p.Q2121R |
| KIPAN | 2 | 109357073 | 109357073 | + | Missense_Mutation | SNP | G | G | A | TCGA-CW-6093-01A-11D-1669-08 | TCGA-CW-6093-11A-01D-1669-08 | g.chr2:109357073G>A | c.911G>A | c.(910-912)aGt>aAt | p.S304N |
| KIPAN | 2 | 109365421 | 109365421 | + | Missense_Mutation | SNP | A | A | C | TCGA-BP-4993-01A-02D-1421-08 | TCGA-BP-4993-11A-01D-1421-08 | g.chr2:109365421A>C | c.1109A>C | c.(1108-1110)aAa>aCa | p.K370T |
| KIPAN | 2 | 109367746 | 109367746 | + | Missense_Mutation | SNP | C | C | A | TCGA-A3-3322-01A-01W-0886-08 | TCGA-A3-3322-11A-01D-0966-08 | g.chr2:109367746C>A | c.1300C>A | c.(1300-1302)Ctt>Att | p.L434I |
| KIPAN | 2 | 109371408 | 109371408 | + | Missense_Mutation | SNP | G | G | A | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr2:109371408G>A | c.2250G>A | c.(2248-2250)atG>atA | p.M750I |
| KIPAN | 2 | 109379713 | 109379713 | + | Silent | SNP | T | T | C | TCGA-BQ-7058-01A-11D-1961-08 | TCGA-BQ-7058-11A-01D-1961-08 | g.chr2:109379713T>C | c.2718T>C | c.(2716-2718)aaT>aaC | p.N906N |
| KIPAN | 2 | 109379866 | 109379866 | + | Missense_Mutation | SNP | G | G | C | TCGA-CW-5589-01A-01D-1534-10 | TCGA-CW-5589-11A-01D-1535-10 | g.chr2:109379866G>C | c.2871G>C | c.(2869-2871)agG>agC | p.R957S |
| KIPAN | 2 | 109379898 | 109379898 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-4985-01A-01D-1462-08 | TCGA-BP-4985-11A-01D-1462-08 | g.chr2:109379898A>G | c.2903A>G | c.(2902-2904)cAg>cGg | p.Q968R |
| KIPAN | 2 | 109380179 | 109380179 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-MH-A55W-01A-11D-A26P-10 | TCGA-MH-A55W-10A-01D-A26P-10 | g.chr2:109380179delA | c.3184delA | c.(3184-3186)aacfs | p.N1062fs |
| KIPAN | 2 | 109380509 | 109380509 | + | Missense_Mutation | SNP | T | T | G | TCGA-A4-8517-01A-11D-2396-08 | TCGA-A4-8517-10A-01D-2396-08 | g.chr2:109380509T>G | c.3514T>G | c.(3514-3516)Ttt>Gtt | p.F1172V |
| KIPAN | 2 | 109381095 | 109381095 | + | Missense_Mutation | SNP | C | C | T | TCGA-CZ-5466-01A-01D-1501-10 | TCGA-CZ-5466-11A-01D-1501-10 | g.chr2:109381095C>T | c.4100C>T | c.(4099-4101)tCa>tTa | p.S1367L |
| KIPAN | 2 | 109381490 | 109381490 | + | Missense_Mutation | SNP | T | T | C | TCGA-2K-A9WE-01A-11D-A382-10 | TCGA-2K-A9WE-10A-01D-A385-10 | g.chr2:109381490T>C | c.4495T>C | c.(4495-4497)Tgt>Cgt | p.C1499R |
| KIPAN | 2 | 109382975 | 109382975 | + | Missense_Mutation | SNP | G | G | C | TCGA-BP-4977-01A-01D-1462-08 | TCGA-BP-4977-11A-01D-1462-08 | g.chr2:109382975G>C | c.5980G>C | c.(5980-5982)Ggt>Cgt | p.G1994R |
| KIPAN | 2 | 109383218 | 109383218 | + | Missense_Mutation | SNP | A | A | C | TCGA-A4-7288-01A-11D-2136-08 | TCGA-A4-7288-11A-01D-2136-08 | g.chr2:109383218A>C | c.6223A>C | c.(6223-6225)Atg>Ctg | p.M2075L |
| KIPAN | 2 | 109383357 | 109383357 | + | Missense_Mutation | SNP | A | A | G | TCGA-KL-8341-01A-11D-2310-10 | TCGA-KL-8341-11A-01D-2310-10 | g.chr2:109383357A>G | c.6362A>G | c.(6361-6363)cAg>cGg | p.Q2121R |
| KIPAN | 2 | 109383602 | 109383603 | + | Missense_Mutation | DNP | GC | GC | AT | TCGA-CZ-5466-01A-01D-1501-10 | TCGA-CZ-5466-11A-01D-1501-10 | g.chr2:109383602_109383603GC>AT | c.6607_6608GC>AT | c.(6607-6609)GCg>ATg | p.A2203M |
| KIPAN | 2 | 109383605 | 109383605 | + | Missense_Mutation | SNP | G | G | A | TCGA-CZ-5466-01A-01D-1501-10 | TCGA-CZ-5466-11A-01D-1501-10 | g.chr2:109383605G>A | c.6610G>A | c.(6610-6612)Gcc>Acc | p.A2204T |
| KIPAN | 2 | 109384143 | 109384143 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-5107-01A-01D-1421-08 | TCGA-B0-5107-11A-01D-1421-08 | g.chr2:109384143A>G | c.7148A>G | c.(7147-7149)aAt>aGt | p.N2383S |
| KIPAN | 2 | 109384150 | 109384150 | + | Silent | SNP | A | A | G | TCGA-BP-5170-01A-01D-1429-08 | TCGA-BP-5170-11A-01D-1429-08 | g.chr2:109384150A>G | c.7155A>G | c.(7153-7155)agA>agG | p.R2385R |
| KIPAN | 2 | 109392304 | 109392304 | + | Silent | SNP | T | T | C | TCGA-BQ-5877-01A-11D-1589-08 | TCGA-BQ-5877-11A-01D-1589-08 | g.chr2:109392304T>C | c.8409T>C | c.(8407-8409)atT>atC | p.I2803I |
| KIPAN | 2 | 109399079 | 109399079 | + | Missense_Mutation | SNP | T | T | G | TCGA-AL-A5DJ-01A-11D-A26P-10 | TCGA-AL-A5DJ-10A-01D-A26P-10 | g.chr2:109399079T>G | c.9130T>G | c.(9130-9132)Tta>Gta | p.L3044V |
| KIRC | 2 | 109357073 | 109357073 | + | Missense_Mutation | SNP | G | G | A | TCGA-CW-6093-01A-11D-1669-08 | TCGA-CW-6093-11A-01D-1669-08 | g.chr2:109357073G>A | c.911G>A | c.(910-912)aGt>aAt | p.S304N |
| KIRC | 2 | 109365421 | 109365421 | + | Missense_Mutation | SNP | A | A | C | TCGA-BP-4993-01A-02D-1421-08 | TCGA-BP-4993-11A-01D-1421-08 | g.chr2:109365421A>C | c.1109A>C | c.(1108-1110)aAa>aCa | p.K370T |
| KIRC | 2 | 109367746 | 109367746 | + | Missense_Mutation | SNP | C | C | A | TCGA-A3-3322-01A-01W-0886-08 | TCGA-A3-3322-11A-01D-0966-08 | g.chr2:109367746C>A | c.1300C>A | c.(1300-1302)Ctt>Att | p.L434I |
| KIRC | 2 | 109371408 | 109371408 | + | Missense_Mutation | SNP | G | G | A | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr2:109371408G>A | c.2250G>A | c.(2248-2250)atG>atA | p.M750I |
| KIRC | 2 | 109379866 | 109379866 | + | Missense_Mutation | SNP | G | G | C | TCGA-CW-5589-01A-01D-1534-10 | TCGA-CW-5589-11A-01D-1535-10 | g.chr2:109379866G>C | c.2871G>C | c.(2869-2871)agG>agC | p.R957S |
| KIRC | 2 | 109379898 | 109379898 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-4985-01A-01D-1462-08 | TCGA-BP-4985-11A-01D-1462-08 | g.chr2:109379898A>G | c.2903A>G | c.(2902-2904)cAg>cGg | p.Q968R |
| KIRC | 2 | 109381095 | 109381095 | + | Missense_Mutation | SNP | C | C | T | TCGA-CZ-5466-01A-01D-1501-10 | TCGA-CZ-5466-11A-01D-1501-10 | g.chr2:109381095C>T | c.4100C>T | c.(4099-4101)tCa>tTa | p.S1367L |
| KIRC | 2 | 109382975 | 109382975 | + | Missense_Mutation | SNP | G | G | C | TCGA-BP-4977-01A-01D-1462-08 | TCGA-BP-4977-11A-01D-1462-08 | g.chr2:109382975G>C | c.5980G>C | c.(5980-5982)Ggt>Cgt | p.G1994R |
| KIRC | 2 | 109383602 | 109383603 | + | Missense_Mutation | DNP | GC | GC | AT | TCGA-CZ-5466-01A-01D-1501-10 | TCGA-CZ-5466-11A-01D-1501-10 | g.chr2:109383602_109383603GC>AT | c.6607_6608GC>AT | c.(6607-6609)GCg>ATg | p.A2203M |
| KIRC | 2 | 109383605 | 109383605 | + | Missense_Mutation | SNP | G | G | A | TCGA-CZ-5466-01A-01D-1501-10 | TCGA-CZ-5466-11A-01D-1501-10 | g.chr2:109383605G>A | c.6610G>A | c.(6610-6612)Gcc>Acc | p.A2204T |
| KIRC | 2 | 109384143 | 109384143 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-5107-01A-01D-1421-08 | TCGA-B0-5107-11A-01D-1421-08 | g.chr2:109384143A>G | c.7148A>G | c.(7147-7149)aAt>aGt | p.N2383S |
| KIRC | 2 | 109384150 | 109384150 | + | Silent | SNP | A | A | G | TCGA-BP-5170-01A-01D-1429-08 | TCGA-BP-5170-11A-01D-1429-08 | g.chr2:109384150A>G | c.7155A>G | c.(7153-7155)agA>agG | p.R2385R |
| KIRP | 2 | 109379713 | 109379713 | + | Silent | SNP | T | T | C | TCGA-BQ-7058-01A-11D-1961-08 | TCGA-BQ-7058-11A-01D-1961-08 | g.chr2:109379713T>C | c.2718T>C | c.(2716-2718)aaT>aaC | p.N906N |
| KIRP | 2 | 109380179 | 109380179 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-MH-A55W-01A-11D-A26P-10 | TCGA-MH-A55W-10A-01D-A26P-10 | g.chr2:109380179delA | c.3184delA | c.(3184-3186)aacfs | p.N1062fs |
| KIRP | 2 | 109380509 | 109380509 | + | Missense_Mutation | SNP | T | T | G | TCGA-A4-8517-01A-11D-2396-08 | TCGA-A4-8517-10A-01D-2396-08 | g.chr2:109380509T>G | c.3514T>G | c.(3514-3516)Ttt>Gtt | p.F1172V |
| KIRP | 2 | 109381490 | 109381490 | + | Missense_Mutation | SNP | T | T | C | TCGA-2K-A9WE-01A-11D-A382-10 | TCGA-2K-A9WE-10A-01D-A385-10 | g.chr2:109381490T>C | c.4495T>C | c.(4495-4497)Tgt>Cgt | p.C1499R |
| KIRP | 2 | 109383218 | 109383218 | + | Missense_Mutation | SNP | A | A | C | TCGA-A4-7288-01A-11D-2136-08 | TCGA-A4-7288-11A-01D-2136-08 | g.chr2:109383218A>C | c.6223A>C | c.(6223-6225)Atg>Ctg | p.M2075L |
| KIRP | 2 | 109392304 | 109392304 | + | Silent | SNP | T | T | C | TCGA-BQ-5877-01A-11D-1589-08 | TCGA-BQ-5877-11A-01D-1589-08 | g.chr2:109392304T>C | c.8409T>C | c.(8407-8409)atT>atC | p.I2803I |
| KIRP | 2 | 109399079 | 109399079 | + | Missense_Mutation | SNP | T | T | G | TCGA-AL-A5DJ-01A-11D-A26P-10 | TCGA-AL-A5DJ-10A-01D-A26P-10 | g.chr2:109399079T>G | c.9130T>G | c.(9130-9132)Tta>Gta | p.L3044V |
| LGG | 2 | 109357066 | 109357066 | + | Missense_Mutation | SNP | C | C | A | TCGA-E1-A7Z4-01A-11D-A34J-08 | TCGA-E1-A7Z4-10A-01D-A34M-08 | g.chr2:109357066C>A | c.904C>A | c.(904-906)Cag>Aag | p.Q302K |
| LGG | 2 | 109365547 | 109365547 | + | Missense_Mutation | SNP | G | G | A | TCGA-WH-A86K-01A-11D-A36O-08 | TCGA-WH-A86K-10A-01D-A367-08 | g.chr2:109365547G>A | c.1235G>A | c.(1234-1236)cGa>cAa | p.R412Q |
| LGG | 2 | 109365585 | 109365585 | + | Splice_Site | SNP | G | G | T | TCGA-HT-8012-01A-11D-2395-08 | TCGA-HT-8012-10A-01D-2396-08 | g.chr2:109365585G>T | c.1273G>T | c.(1273-1275)Ggt>Tgt | p.G425C |
| LGG | 2 | 109368336 | 109368336 | + | Silent | SNP | C | C | T | TCGA-TQ-A7RW-01A-11D-A33T-08 | TCGA-TQ-A7RW-10A-01D-A33W-08 | g.chr2:109368336C>T | c.1641C>T | c.(1639-1641)aaC>aaT | p.N547N |
| LGG | 2 | 109368449 | 109368449 | + | Splice_Site | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:109368449C>T | c.1754C>T | c.(1753-1755)aCg>aTg | p.T585M |
| LGG | 2 | 109370354 | 109370354 | + | Missense_Mutation | SNP | A | A | G | TCGA-R8-A73M-01A-11D-A32B-08 | TCGA-R8-A73M-10C-01D-A329-08 | g.chr2:109370354A>G | c.2129A>G | c.(2128-2130)tAt>tGt | p.Y710C |
| LGG | 2 | 109380084 | 109380084 | + | Missense_Mutation | SNP | C | C | A | TCGA-VM-A8CB-01A-11D-A36O-08 | TCGA-VM-A8CB-10A-01D-A367-08 | g.chr2:109380084C>A | c.3089C>A | c.(3088-3090)cCt>cAt | p.P1030H |
| LGG | 2 | 109382889 | 109382889 | + | Missense_Mutation | SNP | A | A | G | TCGA-HT-7687-01A-11D-2253-08 | TCGA-HT-7687-10A-01D-2253-08 | g.chr2:109382889A>G | c.5894A>G | c.(5893-5895)gAc>gGc | p.D1965G |
| LGG | 2 | 109382974 | 109382974 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:109382974C>T | c.5979C>T | c.(5977-5979)tcC>tcT | p.S1993S |
| LGG | 2 | 109383056 | 109383056 | + | Missense_Mutation | SNP | G | G | A | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr2:109383056G>A | c.6061G>A | c.(6061-6063)Gaa>Aaa | p.E2021K |
| LGG | 2 | 109383804 | 109383804 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr2:109383804G>T | c.6809G>T | c.(6808-6810)aGt>aTt | p.S2270I |
| LGG | 2 | 109384118 | 109384118 | + | Missense_Mutation | SNP | G | G | A | TCGA-P5-A72U-01A-31D-A32B-08 | TCGA-P5-A72U-10A-01D-A329-08 | g.chr2:109384118G>A | c.7123G>A | c.(7123-7125)Gac>Aac | p.D2375N |
| LGG | 2 | 109384409 | 109384409 | + | Missense_Mutation | SNP | T | T | A | TCGA-WY-A85B-01A-11D-A36O-08 | TCGA-WY-A85B-10A-01D-A367-08 | g.chr2:109384409T>A | c.7414T>A | c.(7414-7416)Tta>Ata | p.L2472I |
| LGG | 2 | 109400287 | 109400287 | + | Missense_Mutation | SNP | T | T | C | TCGA-FG-A4MU-01B-11D-A289-08 | TCGA-FG-A4MU-10A-01D-A289-08 | g.chr2:109400287T>C | c.9605T>C | c.(9604-9606)aTt>aCt | p.I3202T |
| LIHC | 2 | 109347859 | 109347859 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-G3-A25V-01A-11D-A16V-10 | TCGA-G3-A25V-10A-01D-A16V-10 | g.chr2:109347859G>T | c.334G>T | c.(334-336)Gga>Tga | p.G112* |
| LIHC | 2 | 109347864 | 109347864 | + | Missense_Mutation | SNP | A | A | T | TCGA-DD-AAC8-01A-11D-A40R-10 | TCGA-DD-AAC8-10A-01D-A40U-10 | g.chr2:109347864A>T | c.339A>T | c.(337-339)agA>agT | p.R113S |
| LIHC | 2 | 109369517 | 109369517 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CC-A5UE-01A-11D-A28X-10 | TCGA-CC-A5UE-10A-01D-A28X-10 | g.chr2:109369517delA | c.1819delA | c.(1819-1821)aagfs | p.K608fs |
| LIHC | 2 | 109379816 | 109379816 | + | Missense_Mutation | SNP | C | C | A | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr2:109379816C>A | c.2821C>A | c.(2821-2823)Cct>Act | p.P941T |
| LIHC | 2 | 109379840 | 109379840 | + | Missense_Mutation | SNP | C | C | G | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr2:109379840C>G | c.2845C>G | c.(2845-2847)Cct>Gct | p.P949A |
| LIHC | 2 | 109380318 | 109380318 | + | Missense_Mutation | SNP | G | G | T | TCGA-DD-A1EL-01A-11D-A152-10 | TCGA-DD-A1EL-10A-01D-A152-10 | g.chr2:109380318G>T | c.3323G>T | c.(3322-3324)gGa>gTa | p.G1108V |
| LIHC | 2 | 109380447 | 109380447 | + | Missense_Mutation | SNP | A | A | G | TCGA-BC-A10Q-01A-11D-A12Z-10 | TCGA-BC-A10Q-11A-11D-A12Z-10 | g.chr2:109380447A>G | c.3452A>G | c.(3451-3453)aAc>aGc | p.N1151S |
| LIHC | 2 | 109380985 | 109380985 | + | Silent | SNP | T | T | C | TCGA-DD-A73B-01A-12D-A32G-10 | TCGA-DD-A73B-10A-01D-A32G-10 | g.chr2:109380985T>C | c.3990T>C | c.(3988-3990)gaT>gaC | p.D1330D |
| LIHC | 2 | 109381074 | 109381074 | + | Missense_Mutation | SNP | G | G | A | TCGA-BC-A217-01A-11D-A152-10 | TCGA-BC-A217-10A-01D-A152-10 | g.chr2:109381074G>A | c.4079G>A | c.(4078-4080)aGc>aAc | p.S1360N |
| LIHC | 2 | 109381074 | 109381074 | + | Missense_Mutation | SNP | G | G | A | TCGA-DD-A1EE-01A-11D-A12Z-10 | TCGA-DD-A1EE-10A-01D-A12Z-10 | g.chr2:109381074G>A | c.4079G>A | c.(4078-4080)aGc>aAc | p.S1360N |
| LIHC | 2 | 109381547 | 109381547 | + | Missense_Mutation | SNP | C | C | T | TCGA-DD-AACJ-01A-11D-A40R-10 | TCGA-DD-AACJ-10A-01D-A40U-10 | g.chr2:109381547C>T | c.4552C>T | c.(4552-4554)Cct>Tct | p.P1518S |
| LIHC | 2 | 109383255 | 109383255 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-AAE7-01A-11D-A40R-10 | TCGA-DD-AAE7-10A-01D-A40U-10 | g.chr2:109383255A>G | c.6260A>G | c.(6259-6261)cAt>cGt | p.H2087R |
| LIHC | 2 | 109384438 | 109384438 | + | Silent | SNP | T | T | C | TCGA-DD-AADO-01A-11D-A40R-10 | TCGA-DD-AADO-10A-01D-A40U-10 | g.chr2:109384438T>C | c.7443T>C | c.(7441-7443)gaT>gaC | p.D2481D |
| LIHC | 2 | 109392277 | 109392277 | + | Silent | SNP | A | A | G | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr2:109392277A>G | c.8382A>G | c.(8380-8382)gaA>gaG | p.E2794E |
| LUAD | 2 | 109345601 | 109345601 | + | Missense_Mutation | SNP | G | G | C | TCGA-78-8662-01A-11D-2393-08 | TCGA-78-8662-10A-01D-2393-08 | g.chr2:109345601G>C | c.86G>C | c.(85-87)gGa>gCa | p.G29A |
| LUAD | 2 | 109347334 | 109347334 | + | Missense_Mutation | SNP | G | G | A | TCGA-97-7941-01A-11D-2184-08 | TCGA-97-7941-10A-01D-2184-08 | g.chr2:109347334G>A | c.245G>A | c.(244-246)tGt>tAt | p.C82Y |
| LUAD | 2 | 109347872 | 109347872 | + | Missense_Mutation | SNP | A | A | G | TCGA-NJ-A4YI-01A-11D-A25L-08 | TCGA-NJ-A4YI-10A-01D-A25L-08 | g.chr2:109347872A>G | c.347A>G | c.(346-348)tAc>tGc | p.Y116C |
| LUAD | 2 | 109352197 | 109352197 | + | Silent | SNP | G | G | T | TCGA-91-6836-01A-21D-1855-08 | TCGA-91-6836-11A-01D-1855-08 | g.chr2:109352197G>T | c.615G>T | c.(613-615)tcG>tcT | p.S205S |
| LUAD | 2 | 109352661 | 109352661 | + | Silent | SNP | G | G | T | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr2:109352661G>T | c.738G>T | c.(736-738)acG>acT | p.T246T |
| LUAD | 2 | 109365489 | 109365489 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-86-A456-01A-11D-A24D-08 | TCGA-86-A456-10A-01D-A24F-08 | g.chr2:109365489C>T | c.1177C>T | c.(1177-1179)Cag>Tag | p.Q393* |
| LUAD | 2 | 109365543 | 109365543 | + | Missense_Mutation | SNP | G | G | T | TCGA-J2-A4AD-01A-11D-A24D-08 | TCGA-J2-A4AD-10A-01D-A24F-08 | g.chr2:109365543G>T | c.1231G>T | c.(1231-1233)Gta>Tta | p.V411L |
| LUAD | 2 | 109365555 | 109365555 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-53-7813-01A-11D-2167-08 | TCGA-53-7813-10A-01D-2167-08 | g.chr2:109365555G>T | c.1243G>T | c.(1243-1245)Gag>Tag | p.E415* |
| LUAD | 2 | 109367852 | 109367852 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-73-4658-01A-01D-1753-08 | TCGA-73-4658-11A-01D-1753-08 | g.chr2:109367852C>G | c.1406C>G | c.(1405-1407)tCa>tGa | p.S469* |
| LUAD | 2 | 109371430 | 109371430 | + | Missense_Mutation | SNP | G | G | A | TCGA-38-4626-01A-01D-1553-08 | TCGA-38-4626-11A-01D-1553-08 | g.chr2:109371430G>A | c.2272G>A | c.(2272-2274)Gaa>Aaa | p.E758K |
| LUAD | 2 | 109371641 | 109371641 | + | Missense_Mutation | SNP | A | A | G | TCGA-62-8402-01A-11D-2323-08 | TCGA-62-8402-10A-01D-2323-08 | g.chr2:109371641A>G | c.2392A>G | c.(2392-2394)Aaa>Gaa | p.K798E |
| LUAD | 2 | 109371669 | 109371669 | + | Missense_Mutation | SNP | A | A | G | TCGA-62-8402-01A-11D-2323-08 | TCGA-62-8402-10A-01D-2323-08 | g.chr2:109371669A>G | c.2420A>G | c.(2419-2421)cAg>cGg | p.Q807R |
| LUAD | 2 | 109374925 | 109374925 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-6777-01A-11D-1855-08 | TCGA-44-6777-10A-01D-1855-08 | g.chr2:109374925G>T | c.2523G>T | c.(2521-2523)tgG>tgT | p.W841C |
| LUAD | 2 | 109379948 | 109379948 | + | Missense_Mutation | SNP | C | C | G | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr2:109379948C>G | c.2953C>G | c.(2953-2955)Ccg>Gcg | p.P985A |
| LUAD | 2 | 109380142 | 109380142 | + | Silent | SNP | A | A | G | TCGA-38-4631-01A-01D-1753-08 | TCGA-38-4631-11A-01D-1753-08 | g.chr2:109380142A>G | c.3147A>G | c.(3145-3147)ccA>ccG | p.P1049P |
| LUAD | 2 | 109380702 | 109380702 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5941-01A-11D-1753-08 | TCGA-50-5941-10A-01D-1753-08 | g.chr2:109380702G>T | c.3707G>T | c.(3706-3708)cGa>cTa | p.R1236L |
| LUAD | 2 | 109380884 | 109380884 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-17-Z001-01A-01W-0746-08 | TCGA-17-Z001-11A-01W-0746-08 | g.chr2:109380884A>T | c.3889A>T | c.(3889-3891)Aag>Tag | p.K1297* |
| LUAD | 2 | 109381162 | 109381162 | + | Silent | SNP | A | A | T | TCGA-49-4510-01A-01D-1265-08 | TCGA-49-4510-11A-01D-1265-08 | g.chr2:109381162A>T | c.4167A>T | c.(4165-4167)ccA>ccT | p.P1389P |
| LUAD | 2 | 109381205 | 109381205 | + | Missense_Mutation | SNP | G | G | T | TCGA-49-4487-01A-21D-1855-08 | TCGA-49-4487-11A-01D-1855-08 | g.chr2:109381205G>T | c.4210G>T | c.(4210-4212)Gtt>Ttt | p.V1404F |
| LUAD | 2 | 109381301 | 109381301 | + | Missense_Mutation | SNP | A | A | G | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr2:109381301A>G | c.4306A>G | c.(4306-4308)Att>Gtt | p.I1436V |
| LUAD | 2 | 109381580 | 109381580 | + | Missense_Mutation | SNP | A | A | T | TCGA-55-A4DF-01A-11D-A24D-08 | TCGA-55-A4DF-10A-01D-A24F-08 | g.chr2:109381580A>T | c.4585A>T | c.(4585-4587)Agt>Tgt | p.S1529C |
| LUAD | 2 | 109381702 | 109381702 | + | Silent | SNP | G | G | T | TCGA-95-A4VK-01A-11D-A25L-08 | TCGA-95-A4VK-10A-01D-A25L-08 | g.chr2:109381702G>T | c.4707G>T | c.(4705-4707)ccG>ccT | p.P1569P |
| LUAD | 2 | 109381727 | 109381727 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-8207-01A-11D-2238-08 | TCGA-55-8207-10A-01D-2238-08 | g.chr2:109381727G>A | c.4732G>A | c.(4732-4734)Gtt>Att | p.V1578I |
| LUAD | 2 | 109382286 | 109382286 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr2:109382286C>T | c.5291C>T | c.(5290-5292)tCt>tTt | p.S1764F |
| LUAD | 2 | 109382540 | 109382540 | + | Missense_Mutation | SNP | G | G | A | TCGA-50-5941-01A-11D-1753-08 | TCGA-50-5941-10A-01D-1753-08 | g.chr2:109382540G>A | c.5545G>A | c.(5545-5547)Gct>Act | p.A1849T |
| LUAD | 2 | 109382771 | 109382771 | + | Missense_Mutation | SNP | G | G | T | TCGA-78-7539-01A-11D-2063-08 | TCGA-78-7539-10A-01D-2063-08 | g.chr2:109382771G>T | c.5776G>T | c.(5776-5778)Gat>Tat | p.D1926Y |
| LUAD | 2 | 109382946 | 109382946 | + | Missense_Mutation | SNP | G | G | T | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr2:109382946G>T | c.5951G>T | c.(5950-5952)gGt>gTt | p.G1984V |
| LUAD | 2 | 109383078 | 109383078 | + | Missense_Mutation | SNP | G | G | C | TCGA-78-8640-01A-11D-2393-08 | TCGA-78-8640-11A-01D-2393-08 | g.chr2:109383078G>C | c.6083G>C | c.(6082-6084)gGa>gCa | p.G2028A |
| LUAD | 2 | 109383270 | 109383270 | + | Missense_Mutation | SNP | C | C | T | TCGA-17-Z028-01A-01W-0746-08 | TCGA-17-Z028-11A-01W-0746-08 | g.chr2:109383270C>T | c.6275C>T | c.(6274-6276)aCg>aTg | p.T2092M |
| LUAD | 2 | 109383271 | 109383271 | + | Silent | SNP | G | G | T | TCGA-L4-A4E5-01A-11D-A24P-08 | TCGA-L4-A4E5-10A-01D-A24P-08 | g.chr2:109383271G>T | c.6276G>T | c.(6274-6276)acG>acT | p.T2092T |
| LUAD | 2 | 109383283 | 109383283 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-A491-01A-11D-A24D-08 | TCGA-55-A491-10A-01D-A24F-08 | g.chr2:109383283G>T | c.6288G>T | c.(6286-6288)aaG>aaT | p.K2096N |
| LUAD | 2 | 109383771 | 109383771 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-6774-01A-21D-1855-08 | TCGA-44-6774-10A-01D-1855-08 | g.chr2:109383771G>T | c.6776G>T | c.(6775-6777)cGt>cTt | p.R2259L |
| LUAD | 2 | 109384162 | 109384162 | + | Missense_Mutation | SNP | C | C | G | TCGA-44-A4SS-01A-11D-A24P-08 | TCGA-44-A4SS-10A-01D-A24P-08 | g.chr2:109384162C>G | c.7167C>G | c.(7165-7167)gaC>gaG | p.D2389E |
| LUAD | 2 | 109384184 | 109384184 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-6981-01A-11D-1945-08 | TCGA-55-6981-11A-01D-1945-08 | g.chr2:109384184G>C | c.7189G>C | c.(7189-7191)Ggg>Cgg | p.G2397R |
| LUAD | 2 | 109384607 | 109384607 | + | Missense_Mutation | SNP | A | A | T | TCGA-78-7166-01A-12D-2063-08 | TCGA-78-7166-11A-01D-2063-08 | g.chr2:109384607A>T | c.7612A>T | c.(7612-7614)Agt>Tgt | p.S2538C |
| LUAD | 2 | 109384690 | 109384690 | + | Missense_Mutation | SNP | G | G | T | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr2:109384690G>T | c.7695G>T | c.(7693-7695)caG>caT | p.Q2565H |
| LUAD | 2 | 109388295 | 109388295 | + | Missense_Mutation | SNP | G | G | C | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr2:109388295G>C | c.7988G>C | c.(7987-7989)aGa>aCa | p.R2663T |
| LUAD | 2 | 109388981 | 109388981 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-5644-01A-21D-2036-08 | TCGA-44-5644-10A-01D-2036-08 | g.chr2:109388981G>T | c.8057G>T | c.(8056-8058)gGa>gTa | p.G2686V |
| LUAD | 2 | 109398747 | 109398747 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr2:109398747G>C | c.8924G>C | c.(8923-8925)aGa>aCa | p.R2975T |
| LUAD | 2 | 109399221 | 109399221 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4418-01A-01D-1265-08 | TCGA-05-4418-10A-01D-1265-08 | g.chr2:109399221G>T | c.9272G>T | c.(9271-9273)cGg>cTg | p.R3091L |
| LUSC | 2 | 109347290 | 109347290 | + | Silent | SNP | T | T | C | TCGA-66-2766-01A-01D-1522-08 | TCGA-66-2766-11A-01D-1522-08 | g.chr2:109347290T>C | c.201T>C | c.(199-201)ggT>ggC | p.G67G |
| LUSC | 2 | 109365585 | 109365585 | + | Splice_Site | SNP | G | G | T | TCGA-18-3416-01A-01D-0983-08 | TCGA-18-3416-11A-01D-0983-08 | g.chr2:109365585G>T | c.1273G>T | c.(1273-1275)Ggt>Tgt | p.G425C |
| LUSC | 2 | 109378557 | 109378557 | + | Splice_Site | SNP | T | T | G | TCGA-22-4613-01A-01D-1441-08 | TCGA-22-4613-11A-01D-1441-08 | g.chr2:109378557T>G | c.2603T>G | c.(2602-2604)gTt>gGt | p.V868G |
| LUSC | 2 | 109379712 | 109379712 | + | Missense_Mutation | SNP | A | A | G | TCGA-46-3768-01A-01D-0983-08 | TCGA-46-3768-10A-01D-0983-08 | g.chr2:109379712A>G | c.2717A>G | c.(2716-2718)aAt>aGt | p.N906S |
| LUSC | 2 | 109379867 | 109379867 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2767-01A-01D-1522-08 | TCGA-66-2767-11A-01D-1522-08 | g.chr2:109379867G>C | c.2872G>C | c.(2872-2874)Ggt>Cgt | p.G958R |
| LUSC | 2 | 109380026 | 109380026 | + | Missense_Mutation | SNP | C | C | T | TCGA-66-2767-01A-01D-1522-08 | TCGA-66-2767-11A-01D-1522-08 | g.chr2:109380026C>T | c.3031C>T | c.(3031-3033)Ccg>Tcg | p.P1011S |
| LUSC | 2 | 109380371 | 109380371 | + | Missense_Mutation | SNP | C | C | T | TCGA-34-5928-01A-11D-1817-08 | TCGA-34-5928-10A-01D-1817-08 | g.chr2:109380371C>T | c.3376C>T | c.(3376-3378)Cgg>Tgg | p.R1126W |
| LUSC | 2 | 109380809 | 109380809 | + | Missense_Mutation | SNP | G | G | A | TCGA-66-2781-01A-01D-1522-08 | TCGA-66-2781-11A-01D-1522-08 | g.chr2:109380809G>A | c.3814G>A | c.(3814-3816)Gca>Aca | p.A1272T |
| LUSC | 2 | 109381112 | 109381112 | + | Missense_Mutation | SNP | G | G | C | TCGA-60-2713-01A-01D-1522-08 | TCGA-60-2713-11A-01D-1522-08 | g.chr2:109381112G>C | c.4117G>C | c.(4117-4119)Gta>Cta | p.V1373L |
| LUSC | 2 | 109381368 | 109381368 | + | Missense_Mutation | SNP | A | A | G | TCGA-21-1070-01A-01D-1521-08 | TCGA-21-1070-11A-01D-1521-08 | g.chr2:109381368A>G | c.4373A>G | c.(4372-4374)aAa>aGa | p.K1458R |
| LUSC | 2 | 109383184 | 109383184 | + | Silent | SNP | C | C | G | TCGA-34-5928-01A-11D-1817-08 | TCGA-34-5928-10A-01D-1817-08 | g.chr2:109383184C>G | c.6189C>G | c.(6187-6189)ctC>ctG | p.L2063L |
| LUSC | 2 | 109383853 | 109383853 | + | Silent | SNP | G | G | A | TCGA-33-4547-01A-01D-1267-08 | TCGA-33-4547-11A-01D-1267-08 | g.chr2:109383853G>A | c.6858G>A | c.(6856-6858)caG>caA | p.Q2286Q |
| LUSC | 2 | 109384025 | 109384025 | + | Missense_Mutation | SNP | A | A | G | TCGA-18-3414-01A-01D-0983-08 | TCGA-18-3414-11A-01D-0983-08 | g.chr2:109384025A>G | c.7030A>G | c.(7030-7032)Aaa>Gaa | p.K2344E |
| LUSC | 2 | 109384287 | 109384287 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr2:109384287C>A | c.7292C>A | c.(7291-7293)tCg>tAg | p.S2431* |
| LUSC | 2 | 109389037 | 109389037 | + | Splice_Site | SNP | G | G | T | TCGA-39-5027-01A-21D-1817-08 | TCGA-39-5027-11A-01D-1817-08 | g.chr2:109389037G>T | c.8113G>T | c.(8113-8115)Gat>Tat | p.D2705Y |
| LUSC | 2 | 109397776 | 109397776 | + | Missense_Mutation | SNP | C | C | T | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr2:109397776C>T | c.8651C>T | c.(8650-8652)tCa>tTa | p.S2884L |
| LUSC | 2 | 109398838 | 109398838 | + | Missense_Mutation | SNP | G | G | T | TCGA-56-1622-01A-01D-1521-08 | TCGA-56-1622-11A-01D-1521-08 | g.chr2:109398838G>T | c.9015G>T | c.(9013-9015)tgG>tgT | p.W3005C |
| OV | 2 | 109368063 | 109368063 | + | Missense_Mutation | SNP | C | C | T | TCGA-04-1638-01A-01W-0639-09 | TCGA-04-1638-11A-01W-0639-09 | g.chr2:109368063C>T | c.1535C>T | c.(1534-1536)cCg>cTg | p.P512L |
| OV | 2 | 109369927 | 109369927 | + | Missense_Mutation | SNP | G | G | C | TCGA-29-1691-01A-01W-0633-09 | TCGA-29-1691-10A-01W-0633-09 | g.chr2:109369927G>C | c.1963G>C | c.(1963-1965)Gct>Cct | p.A655P |
| OV | 2 | 109381770 | 109381770 | + | Missense_Mutation | SNP | G | G | T | TCGA-61-1895-01A-01W-0639-09 | TCGA-61-1895-11A-01W-0639-09 | g.chr2:109381770G>T | c.4775G>T | c.(4774-4776)aGc>aTc | p.S1592I |
| PAAD | 2 | 109352168 | 109352168 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:109352168G>T | c.586G>T | c.(586-588)Gct>Tct | p.A196S |
| PAAD | 2 | 109367778 | 109367778 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-LB-A7SX-01A-11D-A33T-08 | TCGA-LB-A7SX-10A-01D-A33W-08 | g.chr2:109367778G>A | c.1332G>A | c.(1330-1332)tgG>tgA | p.W444* |
| PAAD | 2 | 109367806 | 109367806 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:109367806C>T | c.1360C>T | c.(1360-1362)Cga>Tga | p.R454* |
| PAAD | 2 | 109371669 | 109371669 | + | Missense_Mutation | SNP | A | A | G | TCGA-HZ-A77O-01A-11D-A33T-08 | TCGA-HZ-A77O-10A-01D-A33W-08 | g.chr2:109371669A>G | c.2420A>G | c.(2419-2421)cAg>cGg | p.Q807R |
| PAAD | 2 | 109371669 | 109371669 | + | Missense_Mutation | SNP | A | A | G | TCGA-IB-A6UF-01A-23D-A33T-08 | TCGA-IB-A6UF-10A-01D-A33W-08 | g.chr2:109371669A>G | c.2420A>G | c.(2419-2421)cAg>cGg | p.Q807R |
| PAAD | 2 | 109371685 | 109371685 | + | Missense_Mutation | SNP | A | A | T | TCGA-2J-AABR-01A-11D-A40W-08 | TCGA-2J-AABR-10A-01D-A40W-08 | g.chr2:109371685A>T | c.2436A>T | c.(2434-2436)aaA>aaT | p.K812N |
| PAAD | 2 | 109371685 | 109371685 | + | Missense_Mutation | SNP | A | A | T | TCGA-FB-A78T-01A-12D-A32N-08 | TCGA-FB-A78T-10A-01D-A32N-08 | g.chr2:109371685A>T | c.2436A>T | c.(2434-2436)aaA>aaT | p.K812N |
| PAAD | 2 | 109371685 | 109371685 | + | Missense_Mutation | SNP | A | A | T | TCGA-HV-AA8V-01A-11D-A40W-08 | TCGA-HV-AA8V-10A-01D-A40W-08 | g.chr2:109371685A>T | c.2436A>T | c.(2434-2436)aaA>aaT | p.K812N |
| PAAD | 2 | 109371685 | 109371685 | + | Missense_Mutation | SNP | A | A | T | TCGA-HZ-A77O-01A-11D-A33T-08 | TCGA-HZ-A77O-10A-01D-A33W-08 | g.chr2:109371685A>T | c.2436A>T | c.(2434-2436)aaA>aaT | p.K812N |
| PAAD | 2 | 109371685 | 109371685 | + | Missense_Mutation | SNP | A | A | T | TCGA-HZ-A9TJ-01A-11D-A40W-08 | TCGA-HZ-A9TJ-10A-01D-A40W-08 | g.chr2:109371685A>T | c.2436A>T | c.(2434-2436)aaA>aaT | p.K812N |
| PAAD | 2 | 109371685 | 109371685 | + | Missense_Mutation | SNP | A | A | T | TCGA-IB-A6UF-01A-23D-A33T-08 | TCGA-IB-A6UF-10A-01D-A33W-08 | g.chr2:109371685A>T | c.2436A>T | c.(2434-2436)aaA>aaT | p.K812N |
| PAAD | 2 | 109371685 | 109371685 | + | Missense_Mutation | SNP | A | A | T | TCGA-LB-A9Q5-01A-11D-A397-08 | TCGA-LB-A9Q5-10A-01D-A39A-08 | g.chr2:109371685A>T | c.2436A>T | c.(2434-2436)aaA>aaT | p.K812N |
| PAAD | 2 | 109371685 | 109371685 | + | Missense_Mutation | SNP | A | A | T | TCGA-XD-AAUL-01A-21D-A397-08 | TCGA-XD-AAUL-10A-01D-A39A-08 | g.chr2:109371685A>T | c.2436A>T | c.(2434-2436)aaA>aaT | p.K812N |
| PAAD | 2 | 109380402 | 109380402 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:109380402G>A | c.3407G>A | c.(3406-3408)gGt>gAt | p.G1136D |
| PAAD | 2 | 109380485 | 109380487 | + | In_Frame_Del | DEL | GAT | GAT | - | TCGA-2J-AABU-01A-11D-A40W-08 | TCGA-2J-AABU-10A-01D-A40W-08 | g.chr2:109380485_109380487delGAT | c.3490_3492delGAT | c.(3490-3492)gatdel | p.D1168del |
| PAAD | 2 | 109380485 | 109380487 | + | In_Frame_Del | DEL | GAT | GAT | - | TCGA-FB-A5VM-01A-11D-A32N-08 | TCGA-FB-A5VM-10A-01D-A32N-08 | g.chr2:109380485_109380487delGAT | c.3490_3492delGAT | c.(3490-3492)gatdel | p.D1168del |
| PAAD | 2 | 109380485 | 109380487 | + | In_Frame_Del | DEL | GAT | GAT | - | TCGA-HV-A7OP-01A-11D-A33T-08 | TCGA-HV-A7OP-10A-01D-A33W-08 | g.chr2:109380485_109380487delGAT | c.3490_3492delGAT | c.(3490-3492)gatdel | p.D1168del |
| PAAD | 2 | 109380485 | 109380487 | + | In_Frame_Del | DEL | GAT | GAT | - | TCGA-US-A776-01A-13D-A33T-08 | TCGA-US-A776-11A-11D-A33W-08 | g.chr2:109380485_109380487delGAT | c.3490_3492delGAT | c.(3490-3492)gatdel | p.D1168del |
| PAAD | 2 | 109382805 | 109382805 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-HZ-A77O-01A-11D-A33T-08 | TCGA-HZ-A77O-10A-01D-A33W-08 | g.chr2:109382805delT | c.5810delT | c.(5809-5811)attfs | p.I1937fs |
| PAAD | 2 | 109383227 | 109383227 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:109383227G>T | c.6232G>T | c.(6232-6234)Gaa>Taa | p.E2078* |
| PAAD | 2 | 109389383 | 109389383 | + | Missense_Mutation | SNP | A | A | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr2:109389383A>C | c.8173A>C | c.(8173-8175)Aaa>Caa | p.K2725Q |
| PCPG | 2 | 109382805 | 109382805 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-RW-A7CZ-01A-11D-A35D-08 | TCGA-RW-A7CZ-10B-01D-A35B-08 | g.chr2:109382805delT | c.5810delT | c.(5809-5811)attfs | p.I1937fs |
| PCPG | 2 | 109384207 | 109384207 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-QR-A6GW-01A-11D-A35D-08 | TCGA-QR-A6GW-10A-01D-A35B-08 | g.chr2:109384207G>A | c.7212G>A | c.(7210-7212)tgG>tgA | p.W2404* |
| PRAD | 2 | 109347896 | 109347897 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-KK-A8I4-01A-11D-A364-08 | TCGA-KK-A8I4-11A-11D-A362-08 | g.chr2:109347896_109347897delTT | c.371_372delTT | c.(370-372)cttfs | p.L124fs |
| PRAD | 2 | 109357021 | 109357021 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr2:109357021G>A | c.859G>A | c.(859-861)Gga>Aga | p.G287R |
| PRAD | 2 | 109365424 | 109365424 | + | Missense_Mutation | SNP | A | A | T | TCGA-G9-7509-01A-11D-A41K-08 | TCGA-G9-7509-10A-01D-A41N-08 | g.chr2:109365424A>T | c.1112A>T | c.(1111-1113)gAg>gTg | p.E371V |
| PRAD | 2 | 109365426 | 109365426 | + | Missense_Mutation | SNP | A | A | G | TCGA-G9-7509-01A-11D-A41K-08 | TCGA-G9-7509-10A-01D-A41N-08 | g.chr2:109365426A>G | c.1114A>G | c.(1114-1116)Att>Gtt | p.I372V |
| PRAD | 2 | 109365442 | 109365442 | + | Missense_Mutation | SNP | C | C | T | TCGA-YL-A8SK-01B-21D-A377-08 | TCGA-YL-A8SK-10A-01D-A37A-08 | g.chr2:109365442C>T | c.1130C>T | c.(1129-1131)gCc>gTc | p.A377V |
| PRAD | 2 | 109365452 | 109365452 | + | Silent | SNP | C | C | T | TCGA-HC-7747-01A-11D-2114-08 | TCGA-HC-7747-10A-01D-2115-08 | g.chr2:109365452C>T | c.1140C>T | c.(1138-1140)agC>agT | p.S380S |
| PRAD | 2 | 109371409 | 109371409 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr2:109371409C>T | c.2251C>T | c.(2251-2253)Cag>Tag | p.Q751* |
| PRAD | 2 | 109382805 | 109382805 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-YL-A8SK-01B-21D-A377-08 | TCGA-YL-A8SK-10A-01D-A37A-08 | g.chr2:109382805delT | c.5810delT | c.(5809-5811)attfs | p.I1937fs |
| PRAD | 2 | 109388168 | 109388168 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr2:109388168delA | c.7861delA | c.(7861-7863)aaafs | p.K2622fs |
| READ | 2 | 109352028 | 109352028 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr2:109352028A>C | c.446A>C | c.(445-447)aAa>aCa | p.K149T |
| READ | 2 | 109368375 | 109368375 | + | Silent | SNP | C | C | T | TCGA-F5-6813-01A-11D-1826-10 | TCGA-F5-6813-10A-01D-1826-10 | g.chr2:109368375C>T | c.1680C>T | c.(1678-1680)aaC>aaT | p.N560N |
| READ | 2 | 109369470 | 109369470 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109369470C>A | c.1772C>A | c.(1771-1773)tCt>tAt | p.S591Y |
| READ | 2 | 109379749 | 109379749 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109379749G>A | c.2754G>A | c.(2752-2754)ccG>ccA | p.P918P |
| READ | 2 | 109380686 | 109380686 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109380686C>T | c.3691C>T | c.(3691-3693)Cgc>Tgc | p.R1231C |
| READ | 2 | 109380930 | 109380930 | + | Missense_Mutation | SNP | T | T | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109380930T>C | c.3935T>C | c.(3934-3936)gTa>gCa | p.V1312A |
| READ | 2 | 109382902 | 109382902 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109382902G>T | c.5907G>T | c.(5905-5907)aaG>aaT | p.K1969N |
| READ | 2 | 109382974 | 109382974 | + | Silent | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109382974C>T | c.5979C>T | c.(5977-5979)tcC>tcT | p.S1993S |
| READ | 2 | 109384117 | 109384117 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr2:109384117G>T | c.7122G>T | c.(7120-7122)agG>agT | p.R2374S |
| READ | 2 | 109384127 | 109384127 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109384127T>G | c.7132T>G | c.(7132-7134)Tta>Gta | p.L2378V |
| READ | 2 | 109384299 | 109384299 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr2:109384299T>G | c.7304T>G | c.(7303-7305)aTt>aGt | p.I2435S |
| SARC | 2 | 109368152 | 109368152 | + | Missense_Mutation | SNP | A | A | G | TCGA-WK-A8XX-01A-11D-A37C-09 | TCGA-WK-A8XX-10A-01D-A37F-09 | g.chr2:109368152A>G | c.1624A>G | c.(1624-1626)Aaa>Gaa | p.K542E |
| SARC | 2 | 109383182 | 109383182 | + | Missense_Mutation | SNP | C | C | T | TCGA-DX-AB2E-01A-11D-A38Z-09 | TCGA-DX-AB2E-10A-01D-A38Z-09 | g.chr2:109383182C>T | c.6187C>T | c.(6187-6189)Ctc>Ttc | p.L2063F |
| SARC | 2 | 109384259 | 109384259 | + | Missense_Mutation | SNP | C | C | T | TCGA-DX-AB2E-01A-11D-A38Z-09 | TCGA-DX-AB2E-10A-01D-A38Z-09 | g.chr2:109384259C>T | c.7264C>T | c.(7264-7266)Cgt>Tgt | p.R2422C |
| SARC | 2 | 109384558 | 109384558 | + | Silent | SNP | T | T | A | TCGA-3B-A9I1-01A-11D-A38Z-09 | TCGA-3B-A9I1-10A-01D-A38Z-09 | g.chr2:109384558T>A | c.7563T>A | c.(7561-7563)gtT>gtA | p.V2521V |
| SKCM | 2 | 109347931 | 109347931 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr2:109347931G>A | | c.e4+1 | |
| SKCM | 2 | 109352090 | 109352090 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr2:109352090C>T | c.508C>T | c.(508-510)Cgg>Tgg | p.R170W |
| SKCM | 2 | 109356974 | 109356974 | + | Missense_Mutation | SNP | C | C | T | TCGA-RP-A695-06A-11D-A30X-08 | TCGA-RP-A695-10A-01D-A30X-08 | g.chr2:109356974C>T | c.812C>T | c.(811-813)tCt>tTt | p.S271F |
| SKCM | 2 | 109365414 | 109365414 | + | Missense_Mutation | SNP | T | T | C | TCGA-GF-A6C8-06A-12D-A30X-08 | TCGA-GF-A6C8-10A-01D-A30X-08 | g.chr2:109365414T>C | c.1102T>C | c.(1102-1104)Ttt>Ctt | p.F368L |
| SKCM | 2 | 109367805 | 109367805 | + | Silent | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr2:109367805C>T | c.1359C>T | c.(1357-1359)atC>atT | p.I453I |
| SKCM | 2 | 109367830 | 109367830 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JI-06A-11D-A21A-08 | TCGA-EE-A3JI-10A-01D-A21A-08 | g.chr2:109367830C>T | c.1384C>T | c.(1384-1386)Cat>Tat | p.H462Y |
| SKCM | 2 | 109370326 | 109370326 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr2:109370326C>T | c.2101C>T | c.(2101-2103)Cct>Tct | p.P701S |
| SKCM | 2 | 109371668 | 109371668 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr2:109371668C>T | c.2419C>T | c.(2419-2421)Cag>Tag | p.Q807* |
| SKCM | 2 | 109374986 | 109374986 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr2:109374986C>T | c.2584C>T | c.(2584-2586)Cat>Tat | p.H862Y |
| SKCM | 2 | 109378609 | 109378609 | + | Silent | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr2:109378609C>T | c.2655C>T | c.(2653-2655)tcC>tcT | p.S885S |
| SKCM | 2 | 109379918 | 109379918 | + | Silent | SNP | T | T | C | TCGA-EE-A2GD-06A-11D-A196-08 | TCGA-EE-A2GD-10A-01D-A198-08 | g.chr2:109379918T>C | c.2923T>C | c.(2923-2925)Ttg>Ctg | p.L975L |
| SKCM | 2 | 109380827 | 109380827 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr2:109380827C>T | c.3832C>T | c.(3832-3834)Cca>Tca | p.P1278S |
| SKCM | 2 | 109381019 | 109381019 | + | Silent | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr2:109381019C>T | c.4024C>T | c.(4024-4026)Ctg>Ttg | p.L1342L |
| SKCM | 2 | 109381664 | 109381664 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JI-06A-11D-A21A-08 | TCGA-EE-A3JI-10A-01D-A21A-08 | g.chr2:109381664G>A | c.4669G>A | c.(4669-4671)Gaa>Aaa | p.E1557K |
| SKCM | 2 | 109382422 | 109382422 | + | Silent | SNP | A | A | C | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr2:109382422A>C | c.5427A>C | c.(5425-5427)ccA>ccC | p.P1809P |
| SKCM | 2 | 109382601 | 109382601 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GM-06B-11D-A196-08 | TCGA-EE-A2GM-10A-01D-A198-08 | g.chr2:109382601C>T | c.5606C>T | c.(5605-5607)tCa>tTa | p.S1869L |
| SKCM | 2 | 109382703 | 109382703 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr2:109382703C>T | c.5708C>T | c.(5707-5709)tCg>tTg | p.S1903L |
| SKCM | 2 | 109382770 | 109382770 | + | Silent | SNP | G | G | A | TCGA-DA-A1I1-06A-12D-A196-08 | TCGA-DA-A1I1-10A-01D-A198-08 | g.chr2:109382770G>A | c.5775G>A | c.(5773-5775)caG>caA | p.Q1925Q |
| SKCM | 2 | 109383173 | 109383173 | + | Missense_Mutation | SNP | T | T | G | TCGA-FS-A4F5-06A-11D-A25O-08 | TCGA-FS-A4F5-10B-01D-A25O-08 | g.chr2:109383173T>G | c.6178T>G | c.(6178-6180)Tta>Gta | p.L2060V |
| SKCM | 2 | 109383182 | 109383182 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr2:109383182C>T | c.6187C>T | c.(6187-6189)Ctc>Ttc | p.L2063F |
| SKCM | 2 | 109383769 | 109383769 | + | Silent | SNP | C | C | T | TCGA-D9-A6EA-06A-11D-A30X-08 | TCGA-D9-A6EA-10A-01D-A30X-08 | g.chr2:109383769C>T | c.6774C>T | c.(6772-6774)ttC>ttT | p.F2258F |
| SKCM | 2 | 109383770 | 109383770 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr2:109383770C>T | c.6775C>T | c.(6775-6777)Cgt>Tgt | p.R2259C |
| SKCM | 2 | 109383802 | 109383802 | + | Silent | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr2:109383802C>T | c.6807C>T | c.(6805-6807)ttC>ttT | p.F2269F |
| SKCM | 2 | 109384184 | 109384184 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GT-06A-12D-A197-08 | TCGA-EE-A2GT-10A-01D-A199-08 | g.chr2:109384184G>A | c.7189G>A | c.(7189-7191)Ggg>Agg | p.G2397R |
| SKCM | 2 | 109384259 | 109384259 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr2:109384259C>T | c.7264C>T | c.(7264-7266)Cgt>Tgt | p.R2422C |
| SKCM | 2 | 109384259 | 109384259 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr2:109384259C>T | c.7264C>T | c.(7264-7266)Cgt>Tgt | p.R2422C |
| SKCM | 2 | 109384422 | 109384422 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A183-06A-11D-A196-08 | TCGA-EE-A183-10A-01D-A198-08 | g.chr2:109384422C>T | c.7427C>T | c.(7426-7428)aCa>aTa | p.T2476I |
| SKCM | 2 | 109384509 | 109384509 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1Q6-06A-11D-A196-08 | TCGA-D3-A1Q6-10A-01D-A198-08 | g.chr2:109384509C>T | c.7514C>T | c.(7513-7515)cCa>cTa | p.P2505L |
| SKCM | 2 | 109384791 | 109384791 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C8-06A-12D-A30X-08 | TCGA-GF-A6C8-10A-01D-A30X-08 | g.chr2:109384791C>T | c.7796C>T | c.(7795-7797)tCc>tTc | p.S2599F |
| SKCM | 2 | 109388184 | 109388184 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A267-06A-21D-A196-08 | TCGA-GN-A267-10A-01D-A198-08 | g.chr2:109388184C>T | c.7877C>T | c.(7876-7878)tCt>tTt | p.S2626F |
| SKCM | 2 | 109389502 | 109389502 | + | Splice_Site | SNP | A | A | C | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr2:109389502A>C | c.8292A>C | c.(8290-8292)caA>caC | p.Q2764H |
| SKCM | 2 | 109398752 | 109398752 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr2:109398752C>T | c.8929C>T | c.(8929-8931)Cag>Tag | p.Q2977* |
| SKCM | 2 | 109400092 | 109400092 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A20H-06A-11D-A197-08 | TCGA-EE-A20H-10A-01D-A199-08 | g.chr2:109400092C>T | c.9410C>T | c.(9409-9411)tCc>tTc | p.S3137F |