| 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 | 7 | 122056123 | 122056123 | + | Missense_Mutation | SNP | G | G | C | TCGA-OR-A5JX-01A-11D-A29I-10 | TCGA-OR-A5JX-10B-01D-A29L-10 | g.chr7:122056123G>C | c.2572C>G | c.(2572-2574)Cat>Gat | p.H858D |
| ACC | 7 | 122130227 | 122130227 | + | Missense_Mutation | SNP | C | C | G | TCGA-OR-A5JF-01A-11D-A29I-10 | TCGA-OR-A5JF-10A-01D-A29L-10 | g.chr7:122130227C>G | c.1760G>C | c.(1759-1761)aGg>aCg | p.R587T |
| BLCA | 7 | 121960345 | 121960345 | + | Silent | SNP | C | C | T | TCGA-ZF-AA4X-01A-11D-A38G-08 | TCGA-ZF-AA4X-10A-01D-A38J-08 | g.chr7:121960345C>T | c.3765G>A | c.(3763-3765)ctG>ctA | p.L1255L |
| BLCA | 7 | 122033257 | 122033257 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A3B8-01A-31D-A20D-08 | TCGA-FD-A3B8-10A-01D-A20D-08 | g.chr7:122033257C>G | c.3001G>C | c.(3001-3003)Gag>Cag | p.E1001Q |
| BLCA | 7 | 122078510 | 122078510 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A43X-01A-11D-A23U-08 | TCGA-FD-A43X-10A-01D-A23U-08 | g.chr7:122078510C>T | c.2361G>A | c.(2359-2361)atG>atA | p.M787I |
| BLCA | 7 | 122091442 | 122091442 | + | Missense_Mutation | SNP | C | C | A | TCGA-SY-A9G5-01A-11D-A38G-08 | TCGA-SY-A9G5-10A-01D-A38J-08 | g.chr7:122091442C>A | c.2274G>T | c.(2272-2274)caG>caT | p.Q758H |
| BLCA | 7 | 122091483 | 122091483 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9SI-01A-11D-A391-08 | TCGA-XF-A9SI-10A-01D-A394-08 | g.chr7:122091483C>G | c.2233G>C | c.(2233-2235)Gag>Cag | p.E745Q |
| BLCA | 7 | 122111491 | 122111491 | + | Silent | SNP | G | G | A | TCGA-ZF-A9RL-01A-11D-A38G-08 | TCGA-ZF-A9RL-10A-01D-A38J-08 | g.chr7:122111491G>A | c.2124C>T | c.(2122-2124)gtC>gtT | p.V708V |
| BLCA | 7 | 122114542 | 122114542 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A6B5-01A-11D-A31L-08 | TCGA-DK-A6B5-10A-01D-A31J-08 | g.chr7:122114542C>G | c.1891G>C | c.(1891-1893)Gat>Cat | p.D631H |
| BLCA | 7 | 122130198 | 122130198 | + | Missense_Mutation | SNP | G | G | A | TCGA-GD-A3OP-01A-21D-A21Z-08 | TCGA-GD-A3OP-10A-01D-A21Z-08 | g.chr7:122130198G>A | c.1789C>T | c.(1789-1791)Cct>Tct | p.P597S |
| BLCA | 7 | 122130270 | 122130270 | + | Missense_Mutation | SNP | C | C | A | TCGA-DK-A3IQ-01A-31D-A20D-08 | TCGA-DK-A3IQ-10A-01D-A20D-08 | g.chr7:122130270C>A | c.1717G>T | c.(1717-1719)Gat>Tat | p.D573Y |
| BLCA | 7 | 122130285 | 122130285 | + | Missense_Mutation | SNP | C | C | A | TCGA-K4-A83P-01A-11D-A34U-08 | TCGA-K4-A83P-10A-01D-A34X-08 | g.chr7:122130285C>A | c.1702G>T | c.(1702-1704)Gta>Tta | p.V568L |
| BLCA | 7 | 122261650 | 122261650 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A43N-01A-11D-A23U-08 | TCGA-FD-A43N-10A-01D-A23U-08 | g.chr7:122261650G>A | c.989C>T | c.(988-990)cCg>cTg | p.P330L |
| BLCA | 7 | 122261661 | 122261661 | + | Silent | SNP | C | C | T | TCGA-FD-A3SR-01A-11D-A22Z-08 | TCGA-FD-A3SR-10A-01D-A22Z-08 | g.chr7:122261661C>T | c.978G>A | c.(976-978)tcG>tcA | p.S326S |
| BLCA | 7 | 122377026 | 122377026 | + | Missense_Mutation | SNP | C | C | T | TCGA-GV-A3QI-01A-11D-A21Z-08 | TCGA-GV-A3QI-10A-01D-A21Z-08 | g.chr7:122377026C>T | c.436G>A | c.(436-438)Gtt>Att | p.V146I |
| BLCA | 7 | 122526107 | 122526107 | + | Silent | SNP | G | G | A | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr7:122526107G>A | c.285C>T | c.(283-285)atC>atT | p.I95I |
| BRCA | 7 | 121960230 | 121960230 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A5XS-01A-11D-A29N-09 | TCGA-AC-A5XS-11A-13D-A29N-09 | g.chr7:121960230C>T | c.3880G>A | c.(3880-3882)Gaa>Aaa | p.E1294K |
| BRCA | 7 | 121985736 | 121985736 | + | Splice_Site | SNP | C | C | G | TCGA-D8-A1J8-01A-11D-A13L-09 | TCGA-D8-A1J8-10A-01D-A13O-09 | g.chr7:121985736C>G | | c.e28-1 | |
| BRCA | 7 | 122078500 | 122078500 | + | Missense_Mutation | SNP | C | C | A | TCGA-AC-A3W5-01A-11D-A228-09 | TCGA-AC-A3W5-10A-01D-A22A-09 | g.chr7:122078500C>A | c.2371G>T | c.(2371-2373)Gcc>Tcc | p.A791S |
| BRCA | 7 | 122111514 | 122111514 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-D8-A1J8-01A-11D-A13L-09 | TCGA-D8-A1J8-10A-01D-A13O-09 | g.chr7:122111514C>A | c.2101G>T | c.(2101-2103)Gaa>Taa | p.E701* |
| BRCA | 7 | 122114548 | 122114548 | + | Missense_Mutation | SNP | C | C | G | TCGA-BH-A0BP-01A-11D-A10Y-09 | TCGA-BH-A0BP-10A-01D-A110-09 | g.chr7:122114548C>G | c.1885G>C | c.(1885-1887)Ggt>Cgt | p.G629R |
| BRCA | 7 | 122153323 | 122153323 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A0AV-01A-31D-A10Y-09 | TCGA-BH-A0AV-10A-01D-A110-09 | g.chr7:122153323G>A | c.1522C>T | c.(1522-1524)Cgt>Tgt | p.R508C |
| BRCA | 7 | 122255307 | 122255307 | + | Missense_Mutation | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr7:122255307C>T | c.1151G>A | c.(1150-1152)cGa>cAa | p.R384Q |
| BRCA | 7 | 122269330 | 122269330 | + | Missense_Mutation | SNP | C | C | G | TCGA-A8-A084-01A-21W-A019-09 | TCGA-A8-A084-10A-01W-A021-09 | g.chr7:122269330C>G | c.839G>C | c.(838-840)cGg>cCg | p.R280P |
| BRCA | 7 | 122526107 | 122526107 | + | Silent | SNP | G | G | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr7:122526107G>T | c.285C>A | c.(283-285)atC>atA | p.I95I |
| CESC | 7 | 122114572 | 122114572 | + | Splice_Site | SNP | C | C | T | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr7:122114572C>T | | c.e13-1 | |
| CESC | 7 | 122255280 | 122255280 | + | Missense_Mutation | SNP | T | T | C | TCGA-C5-A1BE-01B-11D-A13W-08 | TCGA-C5-A1BE-10A-01D-A13W-08 | g.chr7:122255280T>C | c.1178A>G | c.(1177-1179)gAa>gGa | p.E393G |
| COAD | 7 | 121960257 | 121960257 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr7:121960257T>C | c.3853A>G | c.(3853-3855)Att>Gtt | p.I1285V |
| COAD | 7 | 121960374 | 121960374 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:121960374G>A | c.3736C>T | c.(3736-3738)Cga>Tga | p.R1246* |
| COAD | 7 | 121985686 | 121985686 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr7:121985686delT | c.3554delA | c.(3553-3555)aacfs | p.N1185fs |
| COAD | 7 | 122027176 | 122027176 | + | Missense_Mutation | SNP | G | G | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr7:122027176G>T | c.3216C>A | c.(3214-3216)gaC>gaA | p.D1072E |
| COAD | 7 | 122033593 | 122033593 | + | Silent | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:122033593G>T | c.2790C>A | c.(2788-2790)atC>atA | p.I930I |
| COAD | 7 | 122221236 | 122221236 | + | Silent | SNP | T | T | C | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr7:122221236T>C | c.1332A>G | c.(1330-1332)ggA>ggG | p.G444G |
| COAD | 7 | 122261549 | 122261549 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:122261549A>G | c.1090T>C | c.(1090-1092)Tca>Cca | p.S364P |
| COAD | 7 | 122261711 | 122261711 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr7:122261711G>A | c.928C>T | c.(928-930)Cgg>Tgg | p.R310W |
| COAD | 7 | 122303526 | 122303526 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr7:122303526C>T | c.551G>A | c.(550-552)cGt>cAt | p.R184H |
| COAD | 7 | 122303536 | 122303536 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3681-01A-01W-0900-09 | TCGA-AA-3681-10A-01W-0900-09 | g.chr7:122303536T>A | c.541A>T | c.(541-543)Ata>Tta | p.I181L |
| COAD | 7 | 122303552 | 122303552 | + | Missense_Mutation | SNP | T | T | G | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr7:122303552T>G | c.525A>C | c.(523-525)gaA>gaC | p.E175D |
| COAD | 7 | 122303604 | 122303604 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr7:122303604C>T | c.473G>A | c.(472-474)cGa>cAa | p.R158Q |
| COAD | 7 | 122377044 | 122377044 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:122377044C>T | c.418G>A | c.(418-420)Gaa>Aaa | p.E140K |
| COAD | 7 | 122526082 | 122526082 | + | Missense_Mutation | SNP | G | G | T | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr7:122526082G>T | c.310C>A | c.(310-312)Ccc>Acc | p.P104T |
| COADREAD | 7 | 121960257 | 121960257 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr7:121960257T>C | c.3853A>G | c.(3853-3855)Att>Gtt | p.I1285V |
| COADREAD | 7 | 121960374 | 121960374 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:121960374G>A | c.3736C>T | c.(3736-3738)Cga>Tga | p.R1246* |
| COADREAD | 7 | 121985686 | 121985686 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr7:121985686delT | c.3554delA | c.(3553-3555)aacfs | p.N1185fs |
| COADREAD | 7 | 121985693 | 121985693 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:121985693G>A | c.3547C>T | c.(3547-3549)Cgg>Tgg | p.R1183W |
| COADREAD | 7 | 122027176 | 122027176 | + | Missense_Mutation | SNP | G | G | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr7:122027176G>T | c.3216C>A | c.(3214-3216)gaC>gaA | p.D1072E |
| COADREAD | 7 | 122033593 | 122033593 | + | Silent | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:122033593G>T | c.2790C>A | c.(2788-2790)atC>atA | p.I930I |
| COADREAD | 7 | 122047704 | 122047704 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:122047704A>C | c.2636T>G | c.(2635-2637)tTt>tGt | p.F879C |
| COADREAD | 7 | 122221236 | 122221236 | + | Silent | SNP | T | T | C | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr7:122221236T>C | c.1332A>G | c.(1330-1332)ggA>ggG | p.G444G |
| COADREAD | 7 | 122255279 | 122255279 | + | Missense_Mutation | SNP | T | T | G | TCGA-DC-5869-01A-01D-1657-10 | TCGA-DC-5869-10A-01D-1657-10 | g.chr7:122255279T>G | c.1179A>C | c.(1177-1179)gaA>gaC | p.E393D |
| COADREAD | 7 | 122261549 | 122261549 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:122261549A>G | c.1090T>C | c.(1090-1092)Tca>Cca | p.S364P |
| COADREAD | 7 | 122261711 | 122261711 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr7:122261711G>A | c.928C>T | c.(928-930)Cgg>Tgg | p.R310W |
| COADREAD | 7 | 122303293 | 122303293 | + | Missense_Mutation | SNP | G | G | C | TCGA-CI-6622-01A-11D-1826-10 | TCGA-CI-6622-10A-01D-1826-10 | g.chr7:122303293G>C | c.784C>G | c.(784-786)Cag>Gag | p.Q262E |
| COADREAD | 7 | 122303526 | 122303526 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr7:122303526C>T | c.551G>A | c.(550-552)cGt>cAt | p.R184H |
| COADREAD | 7 | 122303536 | 122303536 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3681-01A-01W-0900-09 | TCGA-AA-3681-10A-01W-0900-09 | g.chr7:122303536T>A | c.541A>T | c.(541-543)Ata>Tta | p.I181L |
| COADREAD | 7 | 122303552 | 122303552 | + | Missense_Mutation | SNP | T | T | G | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr7:122303552T>G | c.525A>C | c.(523-525)gaA>gaC | p.E175D |
| COADREAD | 7 | 122303604 | 122303604 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr7:122303604C>T | c.473G>A | c.(472-474)cGa>cAa | p.R158Q |
| COADREAD | 7 | 122377044 | 122377044 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:122377044C>T | c.418G>A | c.(418-420)Gaa>Aaa | p.E140K |
| COADREAD | 7 | 122526082 | 122526082 | + | Missense_Mutation | SNP | G | G | T | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr7:122526082G>T | c.310C>A | c.(310-312)Ccc>Acc | p.P104T |
| ESCA | 7 | 122033528 | 122033528 | + | Missense_Mutation | SNP | C | C | G | TCGA-R6-A6L6-01B-11D-A33E-09 | TCGA-R6-A6L6-10A-01D-A33H-09 | g.chr7:122033528C>G | c.2855G>C | c.(2854-2856)aGa>aCa | p.R952T |
| ESCA | 7 | 122194686 | 122194686 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A4OO-01A-11D-A27G-09 | TCGA-L5-A4OO-11A-12D-A27G-09 | g.chr7:122194686C>T | c.1393G>A | c.(1393-1395)Gtt>Att | p.V465I |
| GBM | 7 | 121960313 | 121960313 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-0781-01B-01D-1696-08 | TCGA-14-0781-10A-01D-1696-08 | g.chr7:121960313C>T | c.3797G>A | c.(3796-3798)cGt>cAt | p.R1266H |
| GBMLGG | 7 | 121960313 | 121960313 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-0781-01B-01D-1696-08 | TCGA-14-0781-10A-01D-1696-08 | g.chr7:121960313C>T | c.3797G>A | c.(3796-3798)cGt>cAt | p.R1266H |
| GBMLGG | 7 | 121965555 | 121965555 | + | Silent | SNP | C | C | G | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr7:121965555C>G | c.3693G>C | c.(3691-3693)ctG>ctC | p.L1231L |
| GBMLGG | 7 | 122047655 | 122047655 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:122047655C>T | c.2685G>A | c.(2683-2685)ccG>ccA | p.P895P |
| GBMLGG | 7 | 122111440 | 122111440 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:122111440C>T | c.2175G>A | c.(2173-2175)gtG>gtA | p.V725V |
| GBMLGG | 7 | 122130306 | 122130306 | + | Missense_Mutation | SNP | C | C | A | TCGA-HW-7495-01A-11D-2024-08 | TCGA-HW-7495-10A-01D-2024-08 | g.chr7:122130306C>A | c.1681G>T | c.(1681-1683)Gct>Tct | p.A561S |
| GBMLGG | 7 | 122261562 | 122261562 | + | Silent | SNP | G | G | A | TCGA-S9-A6WD-01A-12D-A33T-08 | TCGA-S9-A6WD-10A-01D-A33W-08 | g.chr7:122261562G>A | c.1077C>T | c.(1075-1077)tcC>tcT | p.S359S |
| GBMLGG | 7 | 122526096 | 122526096 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:122526096A>G | c.296T>C | c.(295-297)tTc>tCc | p.F99S |
| HNSC | 7 | 121960236 | 121960236 | + | Missense_Mutation | SNP | C | C | T | TCGA-CR-5248-01A-01D-2012-08 | TCGA-CR-5248-10A-01D-2013-08 | g.chr7:121960236C>T | c.3874G>A | c.(3874-3876)Gaa>Aaa | p.E1292K |
| HNSC | 7 | 121960383 | 121960383 | + | Silent | SNP | T | T | G | TCGA-UF-A7J9-01A-12D-A34J-08 | TCGA-UF-A7J9-10A-01D-A34M-08 | g.chr7:121960383T>G | c.3727A>C | c.(3727-3729)Agg>Cgg | p.R1243R |
| HNSC | 7 | 122000987 | 122000987 | + | Missense_Mutation | SNP | G | G | C | TCGA-CQ-A4C6-01A-11D-A25D-08 | TCGA-CQ-A4C6-10A-01D-A25E-08 | g.chr7:122000987G>C | c.3468C>G | c.(3466-3468)ttC>ttG | p.F1156L |
| HNSC | 7 | 122028668 | 122028668 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-6960-01A-41D-2012-08 | TCGA-CV-6960-10A-01D-2013-08 | g.chr7:122028668C>T | c.3133G>A | c.(3133-3135)Gcc>Acc | p.A1045T |
| HNSC | 7 | 122033249 | 122033249 | + | Splice_Site | SNP | C | C | T | TCGA-CN-4734-01A-01D-1434-08 | TCGA-CN-4734-10A-01D-1434-08 | g.chr7:122033249C>T | | c.e22+1 | |
| HNSC | 7 | 122033559 | 122033559 | + | Missense_Mutation | SNP | T | T | G | TCGA-D6-A4ZB-01A-11D-A25D-08 | TCGA-D6-A4ZB-10A-01D-A25E-08 | g.chr7:122033559T>G | c.2824A>C | c.(2824-2826)Atg>Ctg | p.M942L |
| HNSC | 7 | 122047602 | 122047602 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr7:122047602C>T | c.2738G>A | c.(2737-2739)cGa>cAa | p.R913Q |
| HNSC | 7 | 122091450 | 122091450 | + | Missense_Mutation | SNP | C | C | G | TCGA-CN-6024-01A-11D-1683-08 | TCGA-CN-6024-10A-01D-1683-08 | g.chr7:122091450C>G | c.2266G>C | c.(2266-2268)Gaa>Caa | p.E756Q |
| HNSC | 7 | 122111562 | 122111562 | + | Missense_Mutation | SNP | C | C | T | TCGA-CR-6471-01A-11D-1870-08 | TCGA-CR-6471-10A-01D-1870-08 | g.chr7:122111562C>T | c.2053G>A | c.(2053-2055)Ggt>Agt | p.G685S |
| HNSC | 7 | 122130254 | 122130254 | + | Missense_Mutation | SNP | C | C | T | TCGA-P3-A5QF-01A-11D-A28R-08 | TCGA-P3-A5QF-10A-01D-A28U-08 | g.chr7:122130254C>T | c.1733G>A | c.(1732-1734)aGa>aAa | p.R578K |
| HNSC | 7 | 122153341 | 122153341 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CR-7367-01A-11D-2012-08 | TCGA-CR-7367-10A-01D-2013-08 | g.chr7:122153341delA | c.1504delT | c.(1504-1506)tggfs | p.W502fs |
| HNSC | 7 | 122194724 | 122194724 | + | Missense_Mutation | SNP | G | G | C | TCGA-CR-7397-01A-11D-2012-08 | TCGA-CR-7397-10A-01D-2013-08 | g.chr7:122194724G>C | c.1355C>G | c.(1354-1356)tCt>tGt | p.S452C |
| HNSC | 7 | 122221318 | 122221318 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-7242-01A-11D-2012-08 | TCGA-CV-7242-10A-01D-2013-08 | g.chr7:122221318G>T | c.1250C>A | c.(1249-1251)aCc>aAc | p.T417N |
| HNSC | 7 | 122261717 | 122261717 | + | Missense_Mutation | SNP | C | C | G | TCGA-BA-5152-01A-02D-1870-08 | TCGA-BA-5152-10A-01D-1870-08 | g.chr7:122261717C>G | c.922G>C | c.(922-924)Gag>Cag | p.E308Q |
| HNSC | 7 | 122269330 | 122269330 | + | Missense_Mutation | SNP | C | C | A | TCGA-UF-A7JT-01A-11D-A34J-08 | TCGA-UF-A7JT-10A-01D-A34M-08 | g.chr7:122269330C>A | c.839G>T | c.(838-840)cGg>cTg | p.R280L |
| HNSC | 7 | 122303468 | 122303468 | + | Missense_Mutation | SNP | C | C | G | TCGA-F7-8298-01A-11D-2394-08 | TCGA-F7-8298-10A-01D-2394-08 | g.chr7:122303468C>G | c.609G>C | c.(607-609)tgG>tgC | p.W203C |
| KIPAN | 7 | 121960313 | 121960313 | + | Missense_Mutation | SNP | C | C | T | TCGA-WN-AB4C-01A-11D-A42J-10 | TCGA-WN-AB4C-10A-01D-A42M-10 | g.chr7:121960313C>T | c.3797G>A | c.(3796-3798)cGt>cAt | p.R1266H |
| KIPAN | 7 | 122114547 | 122114547 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-B2-5641-01A-01D-1534-10 | TCGA-B2-5641-10A-01D-1535-10 | g.chr7:122114547delC | c.1886delG | c.(1885-1887)ggtfs | p.G629fs |
| KIPAN | 7 | 122130209 | 122130210 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-BQ-5892-01A-11D-1589-08 | TCGA-BQ-5892-11A-01D-1589-08 | g.chr7:122130209_122130210insA | c.1777_1778insT | c.(1777-1779)tatfs | p.Y593fs |
| KIPAN | 7 | 122269335 | 122269335 | + | Silent | SNP | A | A | G | TCGA-BQ-5886-01A-11D-1589-08 | TCGA-BQ-5886-11A-01D-1589-08 | g.chr7:122269335A>G | c.834T>C | c.(832-834)gaT>gaC | p.D278D |
| KIRC | 7 | 122114547 | 122114547 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-B2-5641-01A-01D-1534-10 | TCGA-B2-5641-10A-01D-1535-10 | g.chr7:122114547delC | c.1886delG | c.(1885-1887)ggtfs | p.G629fs |
| KIRP | 7 | 121960313 | 121960313 | + | Missense_Mutation | SNP | C | C | T | TCGA-WN-AB4C-01A-11D-A42J-10 | TCGA-WN-AB4C-10A-01D-A42M-10 | g.chr7:121960313C>T | c.3797G>A | c.(3796-3798)cGt>cAt | p.R1266H |
| KIRP | 7 | 122130209 | 122130210 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-BQ-5892-01A-11D-1589-08 | TCGA-BQ-5892-11A-01D-1589-08 | g.chr7:122130209_122130210insA | c.1777_1778insT | c.(1777-1779)tatfs | p.Y593fs |
| KIRP | 7 | 122269335 | 122269335 | + | Silent | SNP | A | A | G | TCGA-BQ-5886-01A-11D-1589-08 | TCGA-BQ-5886-11A-01D-1589-08 | g.chr7:122269335A>G | c.834T>C | c.(832-834)gaT>gaC | p.D278D |
| LGG | 7 | 121965555 | 121965555 | + | Silent | SNP | C | C | G | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr7:121965555C>G | c.3693G>C | c.(3691-3693)ctG>ctC | p.L1231L |
| LGG | 7 | 122047655 | 122047655 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:122047655C>T | c.2685G>A | c.(2683-2685)ccG>ccA | p.P895P |
| LGG | 7 | 122111440 | 122111440 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:122111440C>T | c.2175G>A | c.(2173-2175)gtG>gtA | p.V725V |
| LGG | 7 | 122130306 | 122130306 | + | Missense_Mutation | SNP | C | C | A | TCGA-HW-7495-01A-11D-2024-08 | TCGA-HW-7495-10A-01D-2024-08 | g.chr7:122130306C>A | c.1681G>T | c.(1681-1683)Gct>Tct | p.A561S |
| LGG | 7 | 122261562 | 122261562 | + | Silent | SNP | G | G | A | TCGA-S9-A6WD-01A-12D-A33T-08 | TCGA-S9-A6WD-10A-01D-A33W-08 | g.chr7:122261562G>A | c.1077C>T | c.(1075-1077)tcC>tcT | p.S359S |
| LGG | 7 | 122526096 | 122526096 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:122526096A>G | c.296T>C | c.(295-297)tTc>tCc | p.F99S |
| LIHC | 7 | 121985695 | 121985695 | + | Missense_Mutation | SNP | A | A | T | TCGA-DD-AADO-01A-11D-A40R-10 | TCGA-DD-AADO-10A-01D-A40U-10 | g.chr7:121985695A>T | c.3545T>A | c.(3544-3546)gTt>gAt | p.V1182D |
| LIHC | 7 | 122033326 | 122033326 | + | Missense_Mutation | SNP | G | G | T | TCGA-CC-A9FS-01A-11D-A36X-10 | TCGA-CC-A9FS-10A-01D-A370-10 | g.chr7:122033326G>T | c.2932C>A | c.(2932-2934)Cca>Aca | p.P978T |
| LIHC | 7 | 122056186 | 122056186 | + | Missense_Mutation | SNP | G | G | T | TCGA-DD-AACF-01A-11D-A40R-10 | TCGA-DD-AACF-10A-01D-A40U-10 | g.chr7:122056186G>T | c.2509C>A | c.(2509-2511)Ctg>Atg | p.L837M |
| LIHC | 7 | 122255249 | 122255249 | + | Silent | SNP | T | T | C | TCGA-BC-A3KG-01A-11D-A20W-10 | TCGA-BC-A3KG-10A-01D-A20W-10 | g.chr7:122255249T>C | c.1209A>G | c.(1207-1209)gaA>gaG | p.E403E |
| LIHC | 7 | 122303420 | 122303420 | + | Silent | SNP | T | T | C | TCGA-CC-A5UE-01A-11D-A28X-10 | TCGA-CC-A5UE-10A-01D-A28X-10 | g.chr7:122303420T>C | c.657A>G | c.(655-657)aaA>aaG | p.K219K |
| LIHC | 7 | 122526154 | 122526154 | + | Missense_Mutation | SNP | C | C | G | TCGA-DD-A4NI-01A-11D-A27I-10 | TCGA-DD-A4NI-10A-01D-A27I-10 | g.chr7:122526154C>G | c.238G>C | c.(238-240)Gag>Cag | p.E80Q |
| LUAD | 7 | 121985699 | 121985699 | + | Missense_Mutation | SNP | A | A | G | TCGA-73-4668-01A-01D-1265-08 | TCGA-73-4668-11A-01D-1265-08 | g.chr7:121985699A>G | c.3541T>C | c.(3541-3543)Ttt>Ctt | p.F1181L |
| LUAD | 7 | 121985728 | 121985728 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-6851-01A-11D-1945-08 | TCGA-86-6851-10A-01D-1946-08 | g.chr7:121985728C>T | c.3512G>A | c.(3511-3513)gGa>gAa | p.G1171E |
| LUAD | 7 | 122091483 | 122091483 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-6562-01A-11D-1753-08 | TCGA-86-6562-10A-01D-1753-08 | g.chr7:122091483C>G | c.2233G>C | c.(2233-2235)Gag>Cag | p.E745Q |
| LUAD | 7 | 122091530 | 122091530 | + | Splice_Site | SNP | C | C | A | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr7:122091530C>A | | c.e15-1 | |
| LUAD | 7 | 122130324 | 122130324 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-A456-01A-11D-A24D-08 | TCGA-86-A456-10A-01D-A24F-08 | g.chr7:122130324C>A | c.1663G>T | c.(1663-1665)Ggt>Tgt | p.G555C |
| LUAD | 7 | 122131426 | 122131426 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-7574-01A-11D-2036-08 | TCGA-55-7574-10A-01D-2036-08 | g.chr7:122131426C>T | c.1591G>A | c.(1591-1593)Gaa>Aaa | p.E531K |
| LUAD | 7 | 122221323 | 122221323 | + | Silent | SNP | G | G | A | TCGA-69-7765-01A-11D-2167-08 | TCGA-69-7765-10A-01D-2167-08 | g.chr7:122221323G>A | c.1245C>T | c.(1243-1245)ttC>ttT | p.F415F |
| LUAD | 7 | 122221328 | 122221328 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-6987-01A-11D-1945-08 | TCGA-55-6987-11A-01D-1945-08 | g.chr7:122221328C>T | c.1240G>A | c.(1240-1242)Gat>Aat | p.D414N |
| LUAD | 7 | 122261580 | 122261580 | + | Silent | SNP | C | C | T | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr7:122261580C>T | c.1059G>A | c.(1057-1059)gaG>gaA | p.E353E |
| LUAD | 7 | 122261607 | 122261607 | + | Silent | SNP | T | T | C | TCGA-50-6590-01A-12D-1855-08 | TCGA-50-6590-11A-01D-1855-08 | g.chr7:122261607T>C | c.1032A>G | c.(1030-1032)gcA>gcG | p.A344A |
| LUAD | 7 | 122303304 | 122303304 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z053-01A-01W-0747-08 | TCGA-17-Z053-11A-01W-0747-08 | g.chr7:122303304T>C | c.773A>G | c.(772-774)tAt>tGt | p.Y258C |
| LUAD | 7 | 122303495 | 122303495 | + | Missense_Mutation | SNP | C | C | G | TCGA-17-Z056-01A-01W-0747-08 | TCGA-17-Z056-11A-01W-0747-08 | g.chr7:122303495C>G | c.582G>C | c.(580-582)ttG>ttC | p.L194F |
| LUSC | 7 | 121985692 | 121985692 | + | Missense_Mutation | SNP | C | C | G | TCGA-18-3415-01A-01D-0983-08 | TCGA-18-3415-11A-01D-0983-08 | g.chr7:121985692C>G | c.3548G>C | c.(3547-3549)cGg>cCg | p.R1183P |
| LUSC | 7 | 122027211 | 122027211 | + | Missense_Mutation | SNP | C | C | G | TCGA-34-5928-01A-11D-1817-08 | TCGA-34-5928-10A-01D-1817-08 | g.chr7:122027211C>G | c.3181G>C | c.(3181-3183)Gaa>Caa | p.E1061Q |
| LUSC | 7 | 122033251 | 122033251 | + | Splice_Site | SNP | T | T | A | TCGA-66-2758-01A-02D-1522-08 | TCGA-66-2758-11A-01D-1522-08 | g.chr7:122033251T>A | c.3007A>T | c.(3007-3009)Acc>Tcc | p.T1003S |
| LUSC | 7 | 122033627 | 122033627 | + | Missense_Mutation | SNP | C | C | A | TCGA-60-2723-01A-01D-1522-08 | TCGA-60-2723-11A-01D-1522-08 | g.chr7:122033627C>A | c.2756G>T | c.(2755-2757)tGt>tTt | p.C919F |
| LUSC | 7 | 122047603 | 122047603 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-22-5489-01A-01D-1632-08 | TCGA-22-5489-11A-01D-1632-08 | g.chr7:122047603G>A | c.2737C>T | c.(2737-2739)Cga>Tga | p.R913* |
| LUSC | 7 | 122047684 | 122047684 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2788-01A-01D-0983-08 | TCGA-66-2788-11A-01D-0983-08 | g.chr7:122047684C>A | c.2656G>T | c.(2656-2658)Gat>Tat | p.D886Y |
| LUSC | 7 | 122047709 | 122047709 | + | Missense_Mutation | SNP | C | C | A | TCGA-18-3414-01A-01D-0983-08 | TCGA-18-3414-11A-01D-0983-08 | g.chr7:122047709C>A | c.2631G>T | c.(2629-2631)gaG>gaT | p.E877D |
| LUSC | 7 | 122056162 | 122056162 | + | Missense_Mutation | SNP | C | C | G | TCGA-34-5928-01A-11D-1817-08 | TCGA-34-5928-10A-01D-1817-08 | g.chr7:122056162C>G | c.2533G>C | c.(2533-2535)Gag>Cag | p.E845Q |
| LUSC | 7 | 122111562 | 122111562 | + | Missense_Mutation | SNP | C | C | A | TCGA-43-3920-01A-01D-0983-08 | TCGA-43-3920-10A-01D-0983-08 | g.chr7:122111562C>A | c.2053G>T | c.(2053-2055)Ggt>Tgt | p.G685C |
| LUSC | 7 | 122111574 | 122111574 | + | Missense_Mutation | SNP | A | A | G | TCGA-33-4582-01A-01D-1441-08 | TCGA-33-4582-11A-01D-1441-08 | g.chr7:122111574A>G | c.2041T>C | c.(2041-2043)Tgt>Cgt | p.C681R |
| LUSC | 7 | 122111611 | 122111611 | + | Missense_Mutation | SNP | C | C | A | TCGA-46-3769-01A-01D-0983-08 | TCGA-46-3769-10A-01D-0983-08 | g.chr7:122111611C>A | c.2004G>T | c.(2002-2004)tgG>tgT | p.W668C |
| LUSC | 7 | 122114483 | 122114483 | + | Silent | SNP | G | G | A | TCGA-66-2789-01A-01D-0983-08 | TCGA-66-2789-11A-01D-0983-08 | g.chr7:122114483G>A | c.1950C>T | c.(1948-1950)ctC>ctT | p.L650L |
| LUSC | 7 | 122130223 | 122130223 | + | Silent | SNP | G | G | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr7:122130223G>T | c.1764C>A | c.(1762-1764)gcC>gcA | p.A588A |
| LUSC | 7 | 122130267 | 122130267 | + | Missense_Mutation | SNP | C | C | A | TCGA-51-4080-01A-01D-1458-08 | TCGA-51-4080-11A-01D-1458-08 | g.chr7:122130267C>A | c.1720G>T | c.(1720-1722)Gat>Tat | p.D574Y |
| LUSC | 7 | 122261611 | 122261611 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr7:122261611G>C | c.1028C>G | c.(1027-1029)tCt>tGt | p.S343C |
| LUSC | 7 | 122261629 | 122261629 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr7:122261629A>C | c.1010T>G | c.(1009-1011)tTa>tGa | p.L337* |
| LUSC | 7 | 122261657 | 122261657 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2786-01A-01D-1522-08 | TCGA-66-2786-11A-01D-1522-08 | g.chr7:122261657C>A | c.982G>T | c.(982-984)Ggt>Tgt | p.G328C |
| LUSC | 7 | 122303469 | 122303469 | + | Missense_Mutation | SNP | C | C | A | TCGA-46-3767-01A-01D-0983-08 | TCGA-46-3767-10A-01D-0983-08 | g.chr7:122303469C>A | c.608G>T | c.(607-609)tGg>tTg | p.W203L |
| OV | 7 | 122033544 | 122033544 | + | Missense_Mutation | SNP | C | C | T | TCGA-24-1842-01A-01W-0639-09 | TCGA-24-1842-10A-01W-0639-09 | g.chr7:122033544C>T | c.2839G>A | c.(2839-2841)Gcc>Acc | p.A947T |
| OV | 7 | 122269374 | 122269374 | + | Silent | SNP | G | G | A | TCGA-13-0762-01A-01W-0370-10 | TCGA-13-0762-10A-01W-0370-10 | g.chr7:122269374G>A | c.795C>T | c.(793-795)aaC>aaT | p.N265N |
| OV | 7 | 122303605 | 122303605 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-09-1673-01A-01W-0633-09 | TCGA-09-1673-10A-01W-0633-09 | g.chr7:122303605G>A | c.472C>T | c.(472-474)Cga>Tga | p.R158* |
| PAAD | 7 | 122091518 | 122091518 | + | Missense_Mutation | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:122091518A>G | c.2198T>C | c.(2197-2199)aTt>aCt | p.I733T |
| PAAD | 7 | 122377080 | 122377080 | + | Missense_Mutation | SNP | C | C | A | TCGA-2J-AABF-01A-31D-A40W-08 | TCGA-2J-AABF-10A-01D-A40W-08 | g.chr7:122377080C>A | c.382G>T | c.(382-384)Gcc>Tcc | p.A128S |
| PRAD | 7 | 122078450 | 122078450 | + | Silent | SNP | G | G | A | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr7:122078450G>A | c.2421C>T | c.(2419-2421)ctC>ctT | p.L807L |
| PRAD | 7 | 122111518 | 122111518 | + | Silent | SNP | C | C | G | TCGA-YL-A9WH-01A-11D-A377-08 | TCGA-YL-A9WH-10A-01D-A37A-08 | g.chr7:122111518C>G | c.2097G>C | c.(2095-2097)ctG>ctC | p.L699L |
| PRAD | 7 | 122261737 | 122261737 | + | Missense_Mutation | SNP | A | A | G | TCGA-J9-A52C-01A-11D-A26M-08 | TCGA-J9-A52C-10A-01D-A26K-08 | g.chr7:122261737A>G | c.902T>C | c.(901-903)aTg>aCg | p.M301T |
| PRAD | 7 | 122303546 | 122303546 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-QU-A6IL-01A-11D-A31L-08 | TCGA-QU-A6IL-10A-01D-A31J-08 | g.chr7:122303546delA | c.531delT | c.(529-531)tttfs | p.F177fs |
| READ | 7 | 121985693 | 121985693 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:121985693G>A | c.3547C>T | c.(3547-3549)Cgg>Tgg | p.R1183W |
| READ | 7 | 122047704 | 122047704 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:122047704A>C | c.2636T>G | c.(2635-2637)tTt>tGt | p.F879C |
| READ | 7 | 122255279 | 122255279 | + | Missense_Mutation | SNP | T | T | G | TCGA-DC-5869-01A-01D-1657-10 | TCGA-DC-5869-10A-01D-1657-10 | g.chr7:122255279T>G | c.1179A>C | c.(1177-1179)gaA>gaC | p.E393D |
| READ | 7 | 122303293 | 122303293 | + | Missense_Mutation | SNP | G | G | C | TCGA-CI-6622-01A-11D-1826-10 | TCGA-CI-6622-10A-01D-1826-10 | g.chr7:122303293G>C | c.784C>G | c.(784-786)Cag>Gag | p.Q262E |
| SARC | 7 | 122526253 | 122526253 | + | Missense_Mutation | SNP | G | G | T | TCGA-DX-A6BF-01A-11D-A307-09 | TCGA-DX-A6BF-10A-01D-A307-09 | g.chr7:122526253G>T | c.139C>A | c.(139-141)Cgc>Agc | p.R47S |
| SKCM | 7 | 121960249 | 121960249 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2J9-06A-11D-A196-08 | TCGA-D3-A2J9-10A-01D-A198-08 | g.chr7:121960249C>T | c.3861G>A | c.(3859-3861)atG>atA | p.M1287I |
| SKCM | 7 | 121960374 | 121960374 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:121960374G>A | c.3736C>T | c.(3736-3738)Cga>Tga | p.R1246* |
| SKCM | 7 | 121960381 | 121960381 | + | Silent | SNP | C | C | T | TCGA-D9-A1JW-06A-11D-A19A-08 | TCGA-D9-A1JW-10A-01D-A19A-08 | g.chr7:121960381C>T | c.3729G>A | c.(3727-3729)agG>agA | p.R1243R |
| SKCM | 7 | 121960387 | 121960387 | + | Silent | SNP | G | G | A | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr7:121960387G>A | c.3723C>T | c.(3721-3723)acC>acT | p.T1241T |
| SKCM | 7 | 121985671 | 121985671 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr7:121985671C>T | c.3569G>A | c.(3568-3570)cGa>cAa | p.R1190Q |
| SKCM | 7 | 121985724 | 121985724 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51R-06A-11D-A25O-08 | TCGA-D3-A51R-10A-01D-A25O-08 | g.chr7:121985724C>T | c.3516G>A | c.(3514-3516)atG>atA | p.M1172I |
| SKCM | 7 | 122001057 | 122001057 | + | Missense_Mutation | SNP | A | A | C | TCGA-FS-A4F8-06A-11D-A25O-08 | TCGA-FS-A4F8-10B-01D-A25O-08 | g.chr7:122001057A>C | c.3398T>G | c.(3397-3399)gTg>gGg | p.V1133G |
| SKCM | 7 | 122019443 | 122019443 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr7:122019443G>A | c.3366C>T | c.(3364-3366)atC>atT | p.I1122I |
| SKCM | 7 | 122033335 | 122033335 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1Z3-06A-11D-A197-08 | TCGA-FS-A1Z3-10A-01D-A199-08 | g.chr7:122033335G>A | c.2923C>T | c.(2923-2925)Cca>Tca | p.P975S |
| SKCM | 7 | 122033545 | 122033545 | + | Silent | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr7:122033545G>A | c.2838C>T | c.(2836-2838)atC>atT | p.I946I |
| SKCM | 7 | 122033565 | 122033565 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr7:122033565C>T | c.2818G>A | c.(2818-2820)Gat>Aat | p.D940N |
| SKCM | 7 | 122047607 | 122047607 | + | Silent | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr7:122047607G>A | c.2733C>T | c.(2731-2733)ttC>ttT | p.F911F |
| SKCM | 7 | 122078450 | 122078450 | + | Silent | SNP | G | G | A | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr7:122078450G>A | c.2421C>T | c.(2419-2421)ctC>ctT | p.L807L |
| SKCM | 7 | 122078506 | 122078506 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr7:122078506C>T | c.2365G>A | c.(2365-2367)Gat>Aat | p.D789N |
| SKCM | 7 | 122091457 | 122091457 | + | Silent | SNP | G | G | A | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr7:122091457G>A | c.2259C>T | c.(2257-2259)tcC>tcT | p.S753S |
| SKCM | 7 | 122091462 | 122091462 | + | Missense_Mutation | SNP | A | A | G | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr7:122091462A>G | c.2254T>C | c.(2254-2256)Tct>Cct | p.S752P |
| SKCM | 7 | 122091463 | 122091463 | + | Silent | SNP | G | G | A | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr7:122091463G>A | c.2253C>T | c.(2251-2253)ctC>ctT | p.L751L |
| SKCM | 7 | 122111485 | 122111485 | + | Silent | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr7:122111485G>A | c.2130C>T | c.(2128-2130)gaC>gaT | p.D710D |
| SKCM | 7 | 122114438 | 122114438 | + | Silent | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr7:122114438G>A | c.1995C>T | c.(1993-1995)tgC>tgT | p.C665C |
| SKCM | 7 | 122114448 | 122114448 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr7:122114448G>A | c.1985C>T | c.(1984-1986)tCc>tTc | p.S662F |
| SKCM | 7 | 122114506 | 122114506 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:122114506G>A | c.1927C>T | c.(1927-1929)Cat>Tat | p.H643Y |
| SKCM | 7 | 122114563 | 122114563 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29H-06A-12D-A197-08 | TCGA-EE-A29H-10A-01D-A199-08 | g.chr7:122114563G>A | c.1870C>T | c.(1870-1872)Cgt>Tgt | p.R624C |
| SKCM | 7 | 122130171 | 122130171 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A4U4-06A-11D-A32N-08 | TCGA-GN-A4U4-10B-01D-A32N-08 | g.chr7:122130171G>A | c.1816C>T | c.(1816-1818)Cct>Tct | p.P606S |
| SKCM | 7 | 122131379 | 122131379 | + | Silent | SNP | G | G | A | TCGA-EE-A3J8-06A-11D-A20D-08 | TCGA-EE-A3J8-10A-01D-A20D-08 | g.chr7:122131379G>A | c.1638C>T | c.(1636-1638)acC>acT | p.T546T |
| SKCM | 7 | 122194651 | 122194651 | + | Silent | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr7:122194651G>A | c.1428C>T | c.(1426-1428)atC>atT | p.I476I |
| SKCM | 7 | 122194668 | 122194668 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A183-06A-11D-A196-08 | TCGA-EE-A183-10A-01D-A198-08 | g.chr7:122194668C>T | c.1411G>A | c.(1411-1413)Gat>Aat | p.D471N |
| SKCM | 7 | 122221237 | 122221237 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr7:122221237C>T | c.1331G>A | c.(1330-1332)gGa>gAa | p.G444E |
| SKCM | 7 | 122221238 | 122221238 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr7:122221238C>T | c.1330G>A | c.(1330-1332)Gga>Aga | p.G444R |
| SKCM | 7 | 122261582 | 122261582 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:122261582C>T | c.1057G>A | c.(1057-1059)Gag>Aag | p.E353K |
| SKCM | 7 | 122261735 | 122261735 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr7:122261735C>T | c.904G>A | c.(904-906)Gag>Aag | p.E302K |
| SKCM | 7 | 122261757 | 122261757 | + | Silent | SNP | G | G | A | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr7:122261757G>A | c.882C>T | c.(880-882)ccC>ccT | p.P294P |
| SKCM | 7 | 122377021 | 122377021 | + | Silent | SNP | C | C | T | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr7:122377021C>T | c.441G>A | c.(439-441)cgG>cgA | p.R147R |
| SKCM | 7 | 122377072 | 122377072 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:122377072G>A | c.390C>T | c.(388-390)ctC>ctT | p.L130L |
| BLCA | 12 | 75676043 | 75676043 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-G2-A2EF-01A-12D-A18F-08 | TCGA-G2-A2EF-10A-01D-A18F-08 | g.chr12:75676043G>A | c.1657C>T | c.(1657-1659)Caa>Taa | p.Q553* |
| BLCA | 12 | 75683421 | 75683421 | + | Missense_Mutation | SNP | G | G | T | TCGA-XF-A9SY-01A-21D-A42E-08 | TCGA-XF-A9SY-10A-01D-A42H-08 | g.chr12:75683421G>T | c.1432C>A | c.(1432-1434)Cac>Aac | p.H478N |
| BLCA | 12 | 75693620 | 75693620 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-AAN2-01A-11D-A42E-08 | TCGA-XF-AAN2-10A-01D-A42H-08 | g.chr12:75693620G>A | c.908C>T | c.(907-909)tCa>tTa | p.S303L |
| BLCA | 12 | 75698550 | 75698550 | + | Missense_Mutation | SNP | G | G | C | TCGA-S5-AA26-01A-11D-A38G-08 | TCGA-S5-AA26-10A-01D-A38J-08 | g.chr12:75698550G>C | c.823C>G | c.(823-825)Cta>Gta | p.L275V |
| BRCA | 12 | 75685560 | 75685560 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr12:75685560C>T | c.1261G>A | c.(1261-1263)Gaa>Aaa | p.E421K |
| BRCA | 12 | 75692473 | 75692473 | + | Missense_Mutation | SNP | A | A | C | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr12:75692473A>C | c.1095T>G | c.(1093-1095)ttT>ttG | p.F365L |
| BRCA | 12 | 75715242 | 75715242 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A18T-01A-11D-A12B-09 | TCGA-BH-A18T-11A-42D-A12B-09 | g.chr12:75715242C>T | c.463G>A | c.(463-465)Gca>Aca | p.A155T |
| BRCA | 12 | 75716789 | 75716789 | + | Missense_Mutation | SNP | G | G | C | TCGA-D8-A147-01A-11D-A10Y-09 | TCGA-D8-A147-10A-01D-A110-09 | g.chr12:75716789G>C | c.313C>G | c.(313-315)Caa>Gaa | p.Q105E |
| CESC | 12 | 75678767 | 75678767 | + | Missense_Mutation | SNP | C | C | G | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr12:75678767C>G | c.1546G>C | c.(1546-1548)Gaa>Caa | p.E516Q |
| COAD | 12 | 75676116 | 75676116 | + | Silent | SNP | T | T | C | TCGA-F4-6569-01A-11D-1771-10 | TCGA-F4-6569-10A-01D-1771-10 | g.chr12:75676116T>C | c.1584A>G | c.(1582-1584)aaA>aaG | p.K528K |
| COAD | 12 | 75676117 | 75676117 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr12:75676117T>C | c.1583A>G | c.(1582-1584)aAa>aGa | p.K528R |
| COAD | 12 | 75676118 | 75676118 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr12:75676118T>C | c.1582A>G | c.(1582-1584)Aaa>Gaa | p.K528E |
| COAD | 12 | 75676118 | 75676118 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5341-01A-01D-1408-10 | TCGA-CM-5341-10A-01D-1408-10 | g.chr12:75676118T>C | c.1582A>G | c.(1582-1584)Aaa>Gaa | p.K528E |
| COAD | 12 | 75678791 | 75678791 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-5914-01A-11D-1650-10 | TCGA-CK-5914-10A-01D-1650-10 | g.chr12:75678791G>A | c.1522C>T | c.(1522-1524)Cgt>Tgt | p.R508C |
| COAD | 12 | 75678851 | 75678851 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr12:75678851A>G | c.1462T>C | c.(1462-1464)Tct>Cct | p.S488P |
| COAD | 12 | 75683480 | 75683480 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr12:75683480T>C | c.1373A>G | c.(1372-1374)gAc>gGc | p.D458G |
| COAD | 12 | 75687068 | 75687068 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5666-01A-01D-1650-10 | TCGA-A6-5666-10A-01D-1650-10 | g.chr12:75687068C>T | c.1181G>A | c.(1180-1182)cGa>cAa | p.R394Q |
| COAD | 12 | 75687097 | 75687097 | + | Silent | SNP | G | G | A | TCGA-D5-6539-01A-11D-1719-10 | TCGA-D5-6539-10A-01D-1719-10 | g.chr12:75687097G>A | c.1152C>T | c.(1150-1152)agC>agT | p.S384S |
| COAD | 12 | 75687098 | 75687098 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr12:75687098C>T | c.1151G>A | c.(1150-1152)aGc>aAc | p.S384N |
| COAD | 12 | 75693617 | 75693617 | + | Splice_Site | SNP | C | C | T | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr12:75693617C>T | c.911G>A | c.(910-912)cGt>cAt | p.R304H |
| COAD | 12 | 75710124 | 75710124 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr12:75710124C>T | c.616G>A | c.(616-618)Gat>Aat | p.D206N |
| COAD | 12 | 75716994 | 75716994 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr12:75716994C>T | c.197G>A | c.(196-198)cGa>cAa | p.R66Q |
| COADREAD | 12 | 75676116 | 75676116 | + | Silent | SNP | T | T | C | TCGA-F4-6569-01A-11D-1771-10 | TCGA-F4-6569-10A-01D-1771-10 | g.chr12:75676116T>C | c.1584A>G | c.(1582-1584)aaA>aaG | p.K528K |
| COADREAD | 12 | 75676117 | 75676117 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr12:75676117T>C | c.1583A>G | c.(1582-1584)aAa>aGa | p.K528R |
| COADREAD | 12 | 75676118 | 75676118 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr12:75676118T>C | c.1582A>G | c.(1582-1584)Aaa>Gaa | p.K528E |
| COADREAD | 12 | 75676118 | 75676118 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5341-01A-01D-1408-10 | TCGA-CM-5341-10A-01D-1408-10 | g.chr12:75676118T>C | c.1582A>G | c.(1582-1584)Aaa>Gaa | p.K528E |
| COADREAD | 12 | 75678791 | 75678791 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-5914-01A-11D-1650-10 | TCGA-CK-5914-10A-01D-1650-10 | g.chr12:75678791G>A | c.1522C>T | c.(1522-1524)Cgt>Tgt | p.R508C |
| COADREAD | 12 | 75678851 | 75678851 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr12:75678851A>G | c.1462T>C | c.(1462-1464)Tct>Cct | p.S488P |
| COADREAD | 12 | 75683480 | 75683480 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr12:75683480T>C | c.1373A>G | c.(1372-1374)gAc>gGc | p.D458G |
| COADREAD | 12 | 75687068 | 75687068 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5666-01A-01D-1650-10 | TCGA-A6-5666-10A-01D-1650-10 | g.chr12:75687068C>T | c.1181G>A | c.(1180-1182)cGa>cAa | p.R394Q |
| COADREAD | 12 | 75687097 | 75687097 | + | Silent | SNP | G | G | A | TCGA-D5-6539-01A-11D-1719-10 | TCGA-D5-6539-10A-01D-1719-10 | g.chr12:75687097G>A | c.1152C>T | c.(1150-1152)agC>agT | p.S384S |
| COADREAD | 12 | 75687098 | 75687098 | + | Missense_Mutation | SNP | C | C | T | TCGA-AF-6655-01A-11D-1826-10 | TCGA-AF-6655-10A-01D-1826-10 | g.chr12:75687098C>T | c.1151G>A | c.(1150-1152)aGc>aAc | p.S384N |
| COADREAD | 12 | 75687098 | 75687098 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr12:75687098C>T | c.1151G>A | c.(1150-1152)aGc>aAc | p.S384N |
| COADREAD | 12 | 75693617 | 75693617 | + | Splice_Site | SNP | C | C | T | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr12:75693617C>T | c.911G>A | c.(910-912)cGt>cAt | p.R304H |
| COADREAD | 12 | 75710124 | 75710124 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr12:75710124C>T | c.616G>A | c.(616-618)Gat>Aat | p.D206N |
| COADREAD | 12 | 75716994 | 75716994 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr12:75716994C>T | c.197G>A | c.(196-198)cGa>cAa | p.R66Q |
| ESCA | 12 | 75710093 | 75710093 | + | Splice_Site | SNP | G | G | A | TCGA-VR-A8EP-01A-31D-A403-09 | TCGA-VR-A8EP-10B-01D-A403-09 | g.chr12:75710093G>A | c.647C>T | c.(646-648)gCa>gTa | p.A216V |
| ESCA | 12 | 75710108 | 75710108 | + | Missense_Mutation | SNP | G | G | T | TCGA-V5-AASW-01A-11D-A403-09 | TCGA-V5-AASW-10A-01D-A403-09 | g.chr12:75710108G>T | c.632C>A | c.(631-633)gCa>gAa | p.A211E |
| ESCA | 12 | 75716828 | 75716828 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OU-01A-11D-A28B-09 | TCGA-L5-A4OU-11A-11D-A28E-09 | g.chr12:75716828G>T | c.274C>A | c.(274-276)Cca>Aca | p.P92T |
| ESCA | 12 | 75719046 | 75719046 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-L5-A8NI-01A-11D-A37C-09 | TCGA-L5-A8NI-11A-11D-A37F-09 | g.chr12:75719046C>T | c.161G>A | c.(160-162)tGg>tAg | p.W54* |
| GBM | 12 | 75678781 | 75678781 | + | Missense_Mutation | SNP | A | A | G | TCGA-06-2562-01A-01D-1494-08 | TCGA-06-2562-10A-01D-1494-08 | g.chr12:75678781A>G | c.1532T>C | c.(1531-1533)aTt>aCt | p.I511T |
| GBM | 12 | 75692734 | 75692734 | + | Missense_Mutation | SNP | A | A | C | TCGA-06-5415-01A-01D-1486-08 | TCGA-06-5415-10A-01D-1486-08 | g.chr12:75692734A>C | c.924T>G | c.(922-924)gaT>gaG | p.D308E |
| GBMLGG | 12 | 75678781 | 75678781 | + | Missense_Mutation | SNP | A | A | G | TCGA-06-2562-01A-01D-1494-08 | TCGA-06-2562-10A-01D-1494-08 | g.chr12:75678781A>G | c.1532T>C | c.(1531-1533)aTt>aCt | p.I511T |
| GBMLGG | 12 | 75692508 | 75692508 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-HT-8105-01A-11D-2395-08 | TCGA-HT-8105-10A-01D-2396-08 | g.chr12:75692508G>A | c.1060C>T | c.(1060-1062)Cga>Tga | p.R354* |
| GBMLGG | 12 | 75692734 | 75692734 | + | Missense_Mutation | SNP | A | A | C | TCGA-06-5415-01A-01D-1486-08 | TCGA-06-5415-10A-01D-1486-08 | g.chr12:75692734A>C | c.924T>G | c.(922-924)gaT>gaG | p.D308E |
| HNSC | 12 | 75687068 | 75687068 | + | Missense_Mutation | SNP | C | C | A | TCGA-CR-7402-01A-11D-2012-08 | TCGA-CR-7402-10A-01D-2013-08 | g.chr12:75687068C>A | c.1181G>T | c.(1180-1182)cGa>cTa | p.R394L |
| HNSC | 12 | 75692498 | 75692498 | + | Missense_Mutation | SNP | C | C | T | TCGA-BA-5152-01A-02D-1870-08 | TCGA-BA-5152-10A-01D-1870-08 | g.chr12:75692498C>T | c.1070G>A | c.(1069-1071)gGa>gAa | p.G357E |
| HNSC | 12 | 75692714 | 75692714 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-5441-01A-01D-1512-08 | TCGA-CV-5441-11A-01D-1512-08 | g.chr12:75692714C>A | c.944G>T | c.(943-945)gGg>gTg | p.G315V |
| HNSC | 12 | 75693620 | 75693620 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-A6V1-01A-12D-A34J-08 | TCGA-CN-A6V1-10B-01D-A34M-08 | g.chr12:75693620G>A | c.908C>T | c.(907-909)tCa>tTa | p.S303L |
| HNSC | 12 | 75706697 | 75706697 | + | Splice_Site | SNP | T | T | A | TCGA-IQ-A61H-01A-11D-A30E-08 | TCGA-IQ-A61H-10A-01D-A30H-08 | g.chr12:75706697T>A | | c.e8-2 | |
| KIPAN | 12 | 75716783 | 75716783 | + | Missense_Mutation | SNP | G | G | A | TCGA-B8-5550-01A-01D-1534-10 | TCGA-B8-5550-10A-01D-1535-10 | g.chr12:75716783G>A | c.319C>T | c.(319-321)Cca>Tca | p.P107S |
| KIRC | 12 | 75716783 | 75716783 | + | Missense_Mutation | SNP | G | G | A | TCGA-B8-5550-01A-01D-1534-10 | TCGA-B8-5550-10A-01D-1535-10 | g.chr12:75716783G>A | c.319C>T | c.(319-321)Cca>Tca | p.P107S |
| LGG | 12 | 75692508 | 75692508 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-HT-8105-01A-11D-2395-08 | TCGA-HT-8105-10A-01D-2396-08 | g.chr12:75692508G>A | c.1060C>T | c.(1060-1062)Cga>Tga | p.R354* |
| LIHC | 12 | 75678791 | 75678791 | + | Missense_Mutation | SNP | G | G | A | TCGA-WQ-A9G7-01A-11D-A36X-10 | TCGA-WQ-A9G7-10A-01D-A370-10 | g.chr12:75678791G>A | c.1522C>T | c.(1522-1524)Cgt>Tgt | p.R508C |
| LIHC | 12 | 75683540 | 75683540 | + | Missense_Mutation | SNP | T | T | C | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr12:75683540T>C | c.1313A>G | c.(1312-1314)aAa>aGa | p.K438R |
| LIHC | 12 | 75692472 | 75692472 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr12:75692472delA | c.1096delT | c.(1096-1098)tatfs | p.Y366fs |
| LIHC | 12 | 75692559 | 75692559 | + | Splice_Site | SNP | T | T | C | TCGA-G3-A25V-01A-11D-A16V-10 | TCGA-G3-A25V-10A-01D-A16V-10 | g.chr12:75692559T>C | c.1009A>G | c.(1009-1011)Aca>Gca | p.T337A |
| LIHC | 12 | 75716791 | 75716791 | + | Missense_Mutation | SNP | C | C | A | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr12:75716791C>A | c.311G>T | c.(310-312)tGt>tTt | p.C104F |
| LIHC | 12 | 75720286 | 75720286 | + | Missense_Mutation | SNP | C | C | G | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr12:75720286C>G | c.50G>C | c.(49-51)gGa>gCa | p.G17A |
| LUAD | 12 | 75676059 | 75676059 | + | Missense_Mutation | SNP | A | A | C | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr12:75676059A>C | c.1641T>G | c.(1639-1641)tgT>tgG | p.C547W |
| LUAD | 12 | 75676095 | 75676095 | + | Silent | SNP | G | G | A | TCGA-55-8204-01A-11D-2238-08 | TCGA-55-8204-10A-01D-2238-08 | g.chr12:75676095G>A | c.1605C>T | c.(1603-1605)ggC>ggT | p.G535G |
| LUAD | 12 | 75678809 | 75678809 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-1676-01A-01D-0969-08 | TCGA-64-1676-10A-01D-0969-08 | g.chr12:75678809C>A | c.1504G>T | c.(1504-1506)Gat>Tat | p.D502Y |
| LUAD | 12 | 75678818 | 75678818 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-7667-01A-31D-2063-08 | TCGA-44-7667-10A-01D-2063-08 | g.chr12:75678818C>A | c.1495G>T | c.(1495-1497)Ggc>Tgc | p.G499C |
| LUAD | 12 | 75692486 | 75692486 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4432-01A-01D-1265-08 | TCGA-05-4432-10A-01D-1265-08 | g.chr12:75692486C>A | c.1082G>T | c.(1081-1083)cGa>cTa | p.R361L |
| LUAD | 12 | 75692561 | 75692561 | + | Splice_Site | SNP | C | C | G | TCGA-62-A46P-01A-11D-A24D-08 | TCGA-62-A46P-10A-01D-A24F-08 | g.chr12:75692561C>G | | c.e12-1 | |
| LUAD | 12 | 75692720 | 75692720 | + | Missense_Mutation | SNP | A | A | T | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr12:75692720A>T | c.938T>A | c.(937-939)cTc>cAc | p.L313H |
| LUAD | 12 | 75692736 | 75692736 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z030-01A-01W-0746-08 | TCGA-17-Z030-11A-01W-0746-08 | g.chr12:75692736C>A | c.922G>T | c.(922-924)Gat>Tat | p.D308Y |
| LUAD | 12 | 75698574 | 75698574 | + | Missense_Mutation | SNP | G | G | T | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr12:75698574G>T | c.799C>A | c.(799-801)Cct>Act | p.P267T |
| LUAD | 12 | 75706659 | 75706659 | + | Missense_Mutation | SNP | C | C | G | TCGA-44-7669-01A-21D-2063-08 | TCGA-44-7669-10A-01D-2063-08 | g.chr12:75706659C>G | c.685G>C | c.(685-687)Gca>Cca | p.A229P |
| LUSC | 12 | 75687147 | 75687147 | + | Splice_Site | SNP | C | C | T | TCGA-46-6026-01A-11D-1817-08 | TCGA-46-6026-10A-01D-1817-08 | g.chr12:75687147C>T | c.1102G>A | c.(1102-1104)Ggt>Agt | p.G368S |
| OV | 12 | 75676116 | 75676116 | + | Missense_Mutation | SNP | T | T | G | TCGA-23-1022-01A-02W-0488-09 | TCGA-23-1022-10A-01W-0488-09 | g.chr12:75676116T>G | c.1584A>C | c.(1582-1584)aaA>aaC | p.K528N |
| OV | 12 | 75687068 | 75687068 | + | Missense_Mutation | SNP | C | C | T | TCGA-24-1843-01A-01W-0639-09 | TCGA-24-1843-10A-01W-0639-09 | g.chr12:75687068C>T | c.1181G>A | c.(1180-1182)cGa>cAa | p.R394Q |
| OV | 12 | 75687098 | 75687098 | + | Missense_Mutation | SNP | C | C | A | TCGA-61-2097-01A-02W-0722-08 | TCGA-61-2097-11A-01W-0723-08 | g.chr12:75687098C>A | c.1151G>T | c.(1150-1152)aGc>aTc | p.S384I |
| PAAD | 12 | 75678746 | 75678746 | + | Silent | SNP | G | G | T | TCGA-HZ-A77Q-01A-11D-A36O-08 | TCGA-HZ-A77Q-10A-01D-A367-08 | g.chr12:75678746G>T | c.1567C>A | c.(1567-1569)Cga>Aga | p.R523R |
| PAAD | 12 | 75692696 | 75692696 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr12:75692696T>C | c.962A>G | c.(961-963)gAc>gGc | p.D321G |
| PRAD | 12 | 75678791 | 75678791 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr12:75678791G>A | c.1522C>T | c.(1522-1524)Cgt>Tgt | p.R508C |
| READ | 12 | 75687098 | 75687098 | + | Missense_Mutation | SNP | C | C | T | TCGA-AF-6655-01A-11D-1826-10 | TCGA-AF-6655-10A-01D-1826-10 | g.chr12:75687098C>T | c.1151G>A | c.(1150-1152)aGc>aAc | p.S384N |
| SARC | 12 | 75676046 | 75676046 | + | Missense_Mutation | SNP | A | A | T | TCGA-DX-A6BA-01A-11D-A307-09 | TCGA-DX-A6BA-10A-01D-A307-09 | g.chr12:75676046A>T | c.1654T>A | c.(1654-1656)Tct>Act | p.S552T |
| SARC | 12 | 75678836 | 75678836 | + | Silent | SNP | G | G | A | TCGA-DX-A6BF-01A-11D-A307-09 | TCGA-DX-A6BF-10A-01D-A307-09 | g.chr12:75678836G>A | c.1477C>T | c.(1477-1479)Ctg>Ttg | p.L493L |
| SARC | 12 | 75687052 | 75687052 | + | Missense_Mutation | SNP | A | A | T | TCGA-HB-A3YV-01A-11D-A24N-09 | TCGA-HB-A3YV-10A-01D-A24N-09 | g.chr12:75687052A>T | c.1197T>A | c.(1195-1197)gaT>gaA | p.D399E |
| SKCM | 12 | 75683475 | 75683475 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr12:75683475C>T | c.1378G>A | c.(1378-1380)Gaa>Aaa | p.E460K |
| SKCM | 12 | 75683520 | 75683520 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr12:75683520G>A | c.1333C>T | c.(1333-1335)Cgt>Tgt | p.R445C |
| SKCM | 12 | 75685567 | 75685567 | + | Silent | SNP | G | G | A | TCGA-EE-A20B-06A-11D-A196-08 | TCGA-EE-A20B-10A-01D-A198-08 | g.chr12:75685567G>A | c.1254C>T | c.(1252-1254)atC>atT | p.I418I |
| SKCM | 12 | 75698579 | 75698579 | + | Missense_Mutation | SNP | A | A | C | TCGA-EE-A3J4-06A-11D-A20D-08 | TCGA-EE-A3J4-10A-01D-A20D-08 | g.chr12:75698579A>C | c.794T>G | c.(793-795)aTg>aGg | p.M265R |
| SKCM | 12 | 75698650 | 75698650 | + | Silent | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr12:75698650G>A | c.723C>T | c.(721-723)gtC>gtT | p.V241V |