Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.38414790T>CCA358862FGFR1c.1966A>G (p.Lys656Glu)
c.1954A>G (p.Lys652Glu)
n.2859A>G
n.788A>G
n.656A>G
c.2146A>G (p.Lys716Glu)
n.2654A>G
c.1687A>G (p.Lys563Glu)
c.*1612A>G (n.*1612A>G)
c.*1933A>G (n.*1933A>G)
n.3460A>G
c.1693A>G (p.Lys565Glu)
c.1936A>G (p.Lys646Glu)
c.*1016A>G (n.*1016A>G)
c.1699A>G (p.Lys567Glu)
c.1960A>G (p.Lys654Glu)
c.2059A>G (p.Lys687Glu)
n.4245A>G
n.1488A>G
c.166A>G (p.Lys56Glu)
n.512A>G
c.*861A>G (n.*861A>G)
c.1942A>G (p.Lys648Glu)
c.2065A>G (p.Lys689Glu)
c.1798A>G (p.Lys600Glu)
c.1792A>G (p.Lys598Glu)
c.1675A>G (p.Lys559Glu)
c.2053A>G (p.Lys685Glu)
c.1786A>G (p.Lys596Glu)
c.994A>G (p.Lys332Glu)
n.2239A>G
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
8g.38414790T=CA1777534738FGFR1c.1966A= (p.Lys656=)
c.1954A= (p.Lys652=)
n.2859A=
n.788A=
n.656A=
c.2146A= (p.Lys716=)
n.2654A=
c.1687A= (p.Lys563=)
c.*1612A= (n.*1612A=)
c.*1933A= (n.*1933A=)
n.3460A=
c.1693A= (p.Lys565=)
c.1936A= (p.Lys646=)
c.*1016A= (n.*1016A=)
c.1699A= (p.Lys567=)
c.1960A= (p.Lys654=)
c.2059A= (p.Lys687=)
n.4245A=
n.1488A=
c.166A= (p.Lys56=)
n.512A=
c.*861A= (n.*861A=)
c.1942A= (p.Lys648=)
c.2065A= (p.Lys689=)
c.1798A= (p.Lys600=)
c.1792A= (p.Lys598=)
c.1675A= (p.Lys559=)
c.2053A= (p.Lys685=)
c.1786A= (p.Lys596=)
c.994A= (p.Lys332=)
n.2239A=
dbSNP

Number of alleles fetched