| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.38414254G>A | CA269809 | FGFR1 | c.2084C>T (p.Thr695Ile) c.2072C>T (p.Thr691Ile) n.2977C>T n.1324C>T n.774C>T c.2264C>T (p.Thr755Ile) n.2772C>T c.1805C>T (p.Thr602Ile) c.*1730C>T (n.*1730C>T) c.*2051C>T (n.*2051C>T) n.3578C>T c.1811C>T (p.Thr604Ile) c.2054C>T (p.Thr685Ile) c.*1134C>T (n.*1134C>T) c.1817C>T (p.Thr606Ile) c.2078C>T (p.Thr693Ile) c.2177C>T (p.Thr726Ile) n.4363C>T c.284C>T (p.Thr95Ile) c.*979C>T (n.*979C>T) c.2060C>T (p.Thr687Ile) c.2183C>T (p.Thr728Ile) c.1916C>T (p.Thr639Ile) c.1910C>T (p.Thr637Ile) c.1793C>T (p.Thr598Ile) c.2171C>T (p.Thr724Ile) c.1904C>T (p.Thr635Ile) c.1112C>T (p.Thr371Ile) n.2357C>T | ClinVar dbSNP |
| 8 | g.38414254G>C | CA370728939 | FGFR1 | c.2084C>G (p.Thr695Ser) c.2072C>G (p.Thr691Ser) n.2977C>G n.1324C>G n.774C>G c.2264C>G (p.Thr755Ser) n.2772C>G c.1805C>G (p.Thr602Ser) c.*1730C>G (n.*1730C>G) c.*2051C>G (n.*2051C>G) n.3578C>G c.1811C>G (p.Thr604Ser) c.2054C>G (p.Thr685Ser) c.*1134C>G (n.*1134C>G) c.1817C>G (p.Thr606Ser) c.2078C>G (p.Thr693Ser) c.2177C>G (p.Thr726Ser) n.4363C>G c.284C>G (p.Thr95Ser) c.*979C>G (n.*979C>G) c.2060C>G (p.Thr687Ser) c.2183C>G (p.Thr728Ser) c.1916C>G (p.Thr639Ser) c.1910C>G (p.Thr637Ser) c.1793C>G (p.Thr598Ser) c.2171C>G (p.Thr724Ser) c.1904C>G (p.Thr635Ser) c.1112C>G (p.Thr371Ser) n.2357C>G | dbSNP |