Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.28018500G>TCA483042234FLT3c.2508C>A (p.Ile836=)
c.*420C>A (n.*420C>A)
n.2722C>A
c.2451C>A (p.Ile817=)
c.1983C>A (p.Ile661=)
c.2292C>A (p.Ile764=)
c.1629C>A (p.Ile543=)
c.1611C>A (p.Ile537=)
n.2706C>A
dbSNP COSMIC
13g.28018500G>ACA483042233FLT3c.2508C>T (p.Ile836=)
c.*420C>T (n.*420C>T)
n.2722C>T
c.2451C>T (p.Ile817=)
c.1983C>T (p.Ile661=)
c.2292C>T (p.Ile764=)
c.1629C>T (p.Ile543=)
c.1611C>T (p.Ile537=)
n.2706C>T
dbSNP
13g.28018500G>CCA16602446FLT3c.2508C>G (p.Ile836Met)
c.*420C>G (n.*420C>G)
n.2722C>G
c.2451C>G (p.Ile817Met)
c.1983C>G (p.Ile661Met)
c.2292C>G (p.Ile764Met)
c.1629C>G (p.Ile543Met)
c.1611C>G (p.Ile537Met)
n.2706C>G
ClinVar dbSNP COSMIC

Number of alleles fetched