Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.38414892G>CCA10588455FGFR1c.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
8g.38414892G>ACA185882FGFR1c.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

Number of alleles fetched