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 | 16 | 1364365 | 1364365 | + | Silent | SNP | A | A | G | TCGA-OR-A5LJ-01A-11D-A29I-10 | TCGA-OR-A5LJ-10A-01D-A29L-10 | g.chr16:1364365A>G | c.138A>G | c.(136-138)ccA>ccG | p.P46P |
BLCA | 16 | 1374763 | 1374763 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A3IU-01A-11D-A20D-08 | TCGA-DK-A3IU-10A-01D-A20D-08 | g.chr16:1374763G>A | c.446G>A | c.(445-447)cGa>cAa | p.R149Q |
CESC | 16 | 1370260 | 1370260 | + | Missense_Mutation | SNP | G | G | C | TCGA-C5-A2LX-01A-11D-A18J-09 | TCGA-C5-A2LX-10A-01D-A18J-09 | g.chr16:1370260G>C | c.309G>C | c.(307-309)tgG>tgC | p.W103C |
CESC | 16 | 1374764 | 1374764 | + | Silent | SNP | A | A | G | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr16:1374764A>G | c.447A>G | c.(445-447)cgA>cgG | p.R149R |
COAD | 16 | 1364044 | 1364044 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr16:1364044G>A | c.13G>A | c.(13-15)Gcc>Acc | p.A5T |
COAD | 16 | 1364336 | 1364336 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3655-01A-02D-1719-10 | TCGA-AA-3655-11A-01D-1719-10 | g.chr16:1364336A>G | c.109A>G | c.(109-111)Aac>Gac | p.N37D |
COAD | 16 | 1364337 | 1364337 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6541-01A-11D-1719-10 | TCGA-D5-6541-10A-01D-1719-10 | g.chr16:1364337A>G | c.110A>G | c.(109-111)aAc>aGc | p.N37S |
COAD | 16 | 1364356 | 1364356 | + | Silent | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr16:1364356C>T | c.129C>T | c.(127-129)tgC>tgT | p.C43C |
COAD | 16 | 1374749 | 1374749 | + | Silent | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr16:1374749C>T | c.432C>T | c.(430-432)taC>taT | p.Y144Y |
COADREAD | 16 | 1364044 | 1364044 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr16:1364044G>A | c.13G>A | c.(13-15)Gcc>Acc | p.A5T |
COADREAD | 16 | 1364336 | 1364336 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3655-01A-02D-1719-10 | TCGA-AA-3655-11A-01D-1719-10 | g.chr16:1364336A>G | c.109A>G | c.(109-111)Aac>Gac | p.N37D |
COADREAD | 16 | 1364337 | 1364337 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6541-01A-11D-1719-10 | TCGA-D5-6541-10A-01D-1719-10 | g.chr16:1364337A>G | c.110A>G | c.(109-111)aAc>aGc | p.N37S |
COADREAD | 16 | 1364356 | 1364356 | + | Silent | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr16:1364356C>T | c.129C>T | c.(127-129)tgC>tgT | p.C43C |
COADREAD | 16 | 1370198 | 1370198 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr16:1370198C>A | c.247C>A | c.(247-249)Cac>Aac | p.H83N |
COADREAD | 16 | 1374749 | 1374749 | + | Silent | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr16:1374749C>T | c.432C>T | c.(430-432)taC>taT | p.Y144Y |
HNSC | 16 | 1364314 | 1364314 | + | Silent | SNP | A | A | C | TCGA-P3-A6T3-01A-11D-A34J-08 | TCGA-P3-A6T3-10A-01D-A34M-08 | g.chr16:1364314A>C | c.87A>C | c.(85-87)acA>acC | p.T29T |
HNSC | 16 | 1374785 | 1374785 | + | Silent | SNP | G | G | T | TCGA-CN-5356-01A-01D-1434-08 | TCGA-CN-5356-10A-01D-1434-08 | g.chr16:1374785G>T | c.468G>T | c.(466-468)gcG>gcT | p.A156A |
KIPAN | 16 | 1370453 | 1370453 | + | Missense_Mutation | SNP | A | A | G | TCGA-P4-A5EA-01A-11D-A28G-10 | TCGA-P4-A5EA-11A-11D-A28G-10 | g.chr16:1370453A>G | c.348A>G | c.(346-348)atA>atG | p.I116M |
KIRP | 16 | 1370453 | 1370453 | + | Missense_Mutation | SNP | A | A | G | TCGA-P4-A5EA-01A-11D-A28G-10 | TCGA-P4-A5EA-11A-11D-A28G-10 | g.chr16:1370453A>G | c.348A>G | c.(346-348)atA>atG | p.I116M |
LUAD | 16 | 1364038 | 1364038 | + | Missense_Mutation | SNP | G | G | T | TCGA-86-A456-01A-11D-A24D-08 | TCGA-86-A456-10A-01D-A24F-08 | g.chr16:1364038G>T | c.7G>T | c.(7-9)Ggg>Tgg | p.G3W |
LUAD | 16 | 1374771 | 1374771 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z022-01A-01W-0746-08 | TCGA-17-Z022-11A-01W-0746-08 | g.chr16:1374771G>T | c.454G>T | c.(454-456)Gcc>Tcc | p.A152S |
PRAD | 16 | 1365672 | 1365672 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr16:1365672C>T | c.168C>T | c.(166-168)ggC>ggT | p.G56G |
PRAD | 16 | 1370473 | 1370473 | + | Missense_Mutation | SNP | C | C | T | TCGA-EJ-7314-01A-31D-2114-08 | TCGA-EJ-7314-10A-01D-2114-08 | g.chr16:1370473C>T | c.368C>T | c.(367-369)cCa>cTa | p.P123L |
READ | 16 | 1370198 | 1370198 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr16:1370198C>A | c.247C>A | c.(247-249)Cac>Aac | p.H83N |
SARC | 16 | 1364372 | 1364372 | + | Missense_Mutation | SNP | A | A | G | TCGA-DX-AB2Z-01A-11D-A387-09 | TCGA-DX-AB2Z-10A-01D-A38A-09 | g.chr16:1364372A>G | c.145A>G | c.(145-147)Aaa>Gaa | p.K49E |
SKCM | 16 | 1364364 | 1364364 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr16:1364364C>T | c.137C>T | c.(136-138)cCa>cTa | p.P46L |
SKCM | 16 | 1370212 | 1370212 | + | Silent | SNP | C | C | T | TCGA-DA-A1I8-06A-11D-A197-08 | TCGA-DA-A1I8-10A-01D-A199-08 | g.chr16:1370212C>T | c.261C>T | c.(259-261)taC>taT | p.Y87Y |
SKCM | 16 | 1370212 | 1370212 | + | Silent | SNP | C | C | T | TCGA-EB-A5UN-06A-11D-A30X-08 | TCGA-EB-A5UN-10A-01D-A30X-08 | g.chr16:1370212C>T | c.261C>T | c.(259-261)taC>taT | p.Y87Y |
SKCM | 16 | 1370213 | 1370213 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1I8-06A-11D-A197-08 | TCGA-DA-A1I8-10A-01D-A199-08 | g.chr16:1370213C>T | c.262C>T | c.(262-264)Cct>Tct | p.P88S |