Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.38414892G>C | CA10588455 | FGFR1 | c.1864C>G (p.Arg622Gly) c.1852C>G (p.Arg618Gly) n.2757C>G n.686C>G n.554C>G c.2044C>G (p.Arg682Gly) n.2552C>G c.1585C>G (p.Arg529Gly) c.*1510C>G (n.*1510C>G) c.*1831C>G (n.*1831C>G) n.3358C>G c.1591C>G (p.Arg531Gly) c.1834C>G (p.Arg612Gly) c.*914C>G (n.*914C>G) c.1597C>G (p.Arg533Gly) c.1858C>G (p.Arg620Gly) c.1957C>G (p.Arg653Gly) n.4143C>G n.1386C>G c.64C>G (p.Arg22Gly) n.410C>G c.*759C>G (n.*759C>G) c.1840C>G (p.Arg614Gly) c.1963C>G (p.Arg655Gly) c.1696C>G (p.Arg566Gly) c.1690C>G (p.Arg564Gly) c.1573C>G (p.Arg525Gly) c.1951C>G (p.Arg651Gly) c.1684C>G (p.Arg562Gly) c.892C>G (p.Arg298Gly) n.2137C>G | ClinVar dbSNP |
8 | g.38414892G>A | CA185882 | FGFR1 | c.1864C>T (p.Arg622Ter) c.1852C>T (p.Arg618Ter) n.2757C>T n.686C>T n.554C>T c.2044C>T (p.Arg682Ter) n.2552C>T c.1585C>T (p.Arg529Ter) c.*1510C>T (n.*1510C>T) c.*1831C>T (n.*1831C>T) n.3358C>T c.1591C>T (p.Arg531Ter) c.1834C>T (p.Arg612Ter) c.*914C>T (n.*914C>T) c.1597C>T (p.Arg533Ter) c.1858C>T (p.Arg620Ter) c.1957C>T (p.Arg653Ter) n.4143C>T n.1386C>T c.64C>T (p.Arg22Ter) n.410C>T c.*759C>T (n.*759C>T) c.1840C>T (p.Arg614Ter) c.1963C>T (p.Arg655Ter) c.1696C>T (p.Arg566Ter) c.1690C>T (p.Arg564Ter) c.1573C>T (p.Arg525Ter) c.1951C>T (p.Arg651Ter) c.1684C>T (p.Arg562Ter) c.892C>T (p.Arg298Ter) n.2137C>T | ClinVar dbSNP |