Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.38417333T>CCA16602864FGFR1c.1636A>G (p.Asn546Asp)
c.1624A>G (p.Asn542Asp)
n.2529A>G
n.402A>G
c.1816A>G (p.Asn606Asp)
n.2324A>G
c.1357A>G (p.Asn453Asp)
c.*1282A>G (n.*1282A>G)
c.*1603A>G (n.*1603A>G)
n.3130A>G
c.1363A>G (p.Asn455Asp)
c.1606A>G (p.Asn536Asp)
c.*686A>G (n.*686A>G)
c.1369A>G (p.Asn457Asp)
c.1630A>G (p.Asn544Asp)
c.1729A>G (p.Asn577Asp)
n.803A>G
c.1513A>G (n.1513A>G)
n.3915A>G
n.1158A>G
n.182A>G
c.*531A>G (n.*531A>G)
c.1612A>G (p.Asn538Asp)
c.1735A>G (p.Asn579Asp)
c.1468A>G (p.Asn490Asp)
c.1462A>G (p.Asn488Asp)
c.1345A>G (p.Asn449Asp)
c.1723A>G (p.Asn575Asp)
c.1456A>G (p.Asn486Asp)
c.664A>G (p.Asn222Asp)
n.1884A>G
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
8g.38417333T=CA1777536243FGFR1c.1636A= (p.Asn546=)
c.1624A= (p.Asn542=)
n.2529A=
n.402A=
c.1816A= (p.Asn606=)
n.2324A=
c.1357A= (p.Asn453=)
c.*1282A= (n.*1282A=)
c.*1603A= (n.*1603A=)
n.3130A=
c.1363A= (p.Asn455=)
c.1606A= (p.Asn536=)
c.*686A= (n.*686A=)
c.1369A= (p.Asn457=)
c.1630A= (p.Asn544=)
c.1729A= (p.Asn577=)
n.803A=
c.1513A= (n.1513A=)
n.3915A=
n.1158A=
n.182A=
c.*531A= (n.*531A=)
c.1612A= (p.Asn538=)
c.1735A= (p.Asn579=)
c.1468A= (p.Asn490=)
c.1462A= (p.Asn488=)
c.1345A= (p.Asn449=)
c.1723A= (p.Asn575=)
c.1456A= (p.Asn486=)
c.664A= (p.Asn222=)
n.1884A=
dbSNP

Number of alleles fetched