| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.38414265C>A | CA16605223 | FGFR1 | c.2073G>T (p.Trp691Cys) c.2061G>T (p.Trp687Cys) n.2966G>T n.1313G>T n.763G>T c.2253G>T (p.Trp751Cys) n.2761G>T c.1794G>T (p.Trp598Cys) c.*1719G>T (n.*1719G>T) c.*2040G>T (n.*2040G>T) n.3567G>T c.1800G>T (p.Trp600Cys) c.2043G>T (p.Trp681Cys) c.*1123G>T (n.*1123G>T) c.1806G>T (p.Trp602Cys) c.2067G>T (p.Trp689Cys) c.2166G>T (p.Trp722Cys) n.4352G>T c.273G>T (p.Trp91Cys) c.*968G>T (n.*968G>T) c.2049G>T (p.Trp683Cys) c.2172G>T (p.Trp724Cys) c.1905G>T (p.Trp635Cys) c.1899G>T (p.Trp633Cys) c.1782G>T (p.Trp594Cys) c.2160G>T (p.Trp720Cys) c.1893G>T (p.Trp631Cys) c.1101G>T (p.Trp367Cys) n.2346G>T | ClinVar dbSNP |
| 8 | g.38414265C>G | CA370729024 | FGFR1 | c.2073G>C (p.Trp691Cys) c.2061G>C (p.Trp687Cys) n.2966G>C n.1313G>C n.763G>C c.2253G>C (p.Trp751Cys) n.2761G>C c.1794G>C (p.Trp598Cys) c.*1719G>C (n.*1719G>C) c.*2040G>C (n.*2040G>C) n.3567G>C c.1800G>C (p.Trp600Cys) c.2043G>C (p.Trp681Cys) c.*1123G>C (n.*1123G>C) c.1806G>C (p.Trp602Cys) c.2067G>C (p.Trp689Cys) c.2166G>C (p.Trp722Cys) n.4352G>C c.273G>C (p.Trp91Cys) c.*968G>C (n.*968G>C) c.2049G>C (p.Trp683Cys) c.2172G>C (p.Trp724Cys) c.1905G>C (p.Trp635Cys) c.1899G>C (p.Trp633Cys) c.1782G>C (p.Trp594Cys) c.2160G>C (p.Trp720Cys) c.1893G>C (p.Trp631Cys) c.1101G>C (p.Trp367Cys) n.2346G>C | dbSNP |
| 8 | g.38414265C>T | CA370729026 | FGFR1 | c.2073G>A (p.Trp691Ter) c.2061G>A (p.Trp687Ter) n.2966G>A n.1313G>A n.763G>A c.2253G>A (p.Trp751Ter) n.2761G>A c.1794G>A (p.Trp598Ter) c.*1719G>A (n.*1719G>A) c.*2040G>A (n.*2040G>A) n.3567G>A c.1800G>A (p.Trp600Ter) c.2043G>A (p.Trp681Ter) c.*1123G>A (n.*1123G>A) c.1806G>A (p.Trp602Ter) c.2067G>A (p.Trp689Ter) c.2166G>A (p.Trp722Ter) n.4352G>A c.273G>A (p.Trp91Ter) c.*968G>A (n.*968G>A) c.2049G>A (p.Trp683Ter) c.2172G>A (p.Trp724Ter) c.1905G>A (p.Trp635Ter) c.1899G>A (p.Trp633Ter) c.1782G>A (p.Trp594Ter) c.2160G>A (p.Trp720Ter) c.1893G>A (p.Trp631Ter) c.1101G>A (p.Trp367Ter) n.2346G>A | dbSNP |