Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121488052A>TCA16618938FGFR2c.1928T>A (p.Ile643Lys)
c.1919T>A (p.Ile640Lys)
c.749T>A (p.Ile250Lys)
n.1267T>A
c.1574T>A (p.Ile525Lys)
n.745T>A
n.337T>A
c.*627T>A (n.*627T>A)
n.4266T>A
n.2938T>A
c.1925T>A (p.Ile642Lys)
c.1652T>A (p.Ile551Lys)
c.1658T>A (p.Ile553Lys)
c.1661T>A (p.Ile554Lys)
c.1583T>A (p.Ile528Lys)
c.1577T>A (p.Ile526Lys)
c.1589T>A (p.Ile530Lys)
c.701T>A (p.Ile234Lys)
c.1241T>A (p.Ile414Lys)
c.*972T>A (n.*972T>A)
c.1580T>A (p.Ile527Lys)
n.2375T>A
c.1979T>A (p.Ile660Lys)
c.1976T>A (p.Ile659Lys)
c.1985T>A (p.Ile662Lys)
c.1718T>A (p.Ile573Lys)
c.1640T>A (p.Ile547Lys)
c.1982T>A (p.Ile661Lys)
c.1637T>A (p.Ile546Lys)
c.1631T>A (p.Ile544Lys)
c.1715T>A (p.Ile572Lys)
c.1712T>A (p.Ile571Lys)
c.1709T>A (p.Ile570Lys)
c.755T>A (p.Ile252Lys)
n.2361T>A
ClinVar dbSNP
10g.121488052A>CCA378314675FGFR2c.1928T>G (p.Ile643Arg)
c.1919T>G (p.Ile640Arg)
c.749T>G (p.Ile250Arg)
n.1267T>G
c.1574T>G (p.Ile525Arg)
n.745T>G
n.337T>G
c.*627T>G (n.*627T>G)
n.4266T>G
n.2938T>G
c.1925T>G (p.Ile642Arg)
c.1652T>G (p.Ile551Arg)
c.1658T>G (p.Ile553Arg)
c.1661T>G (p.Ile554Arg)
c.1583T>G (p.Ile528Arg)
c.1577T>G (p.Ile526Arg)
c.1589T>G (p.Ile530Arg)
c.701T>G (p.Ile234Arg)
c.1241T>G (p.Ile414Arg)
c.*972T>G (n.*972T>G)
c.1580T>G (p.Ile527Arg)
n.2375T>G
c.1979T>G (p.Ile660Arg)
c.1976T>G (p.Ile659Arg)
c.1985T>G (p.Ile662Arg)
c.1718T>G (p.Ile573Arg)
c.1640T>G (p.Ile547Arg)
c.1982T>G (p.Ile661Arg)
c.1637T>G (p.Ile546Arg)
c.1631T>G (p.Ile544Arg)
c.1715T>G (p.Ile572Arg)
c.1712T>G (p.Ile571Arg)
c.1709T>G (p.Ile570Arg)
c.755T>G (p.Ile252Arg)
n.2361T>G
dbSNP

Number of alleles fetched