Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.28018501A>CCA16603127FLT3c.2507T>G (p.Ile836Ser)
c.*419T>G (n.*419T>G)
n.2721T>G
c.2450T>G (p.Ile817Ser)
c.1982T>G (p.Ile661Ser)
c.2291T>G (p.Ile764Ser)
c.1628T>G (p.Ile543Ser)
c.1610T>G (p.Ile537Ser)
n.2705T>G
ClinVar dbSNP COSMIC
13g.28018501A>TCA387650199FLT3c.2507T>A (p.Ile836Asn)
c.*419T>A (n.*419T>A)
n.2721T>A
c.2450T>A (p.Ile817Asn)
c.1982T>A (p.Ile661Asn)
c.2291T>A (p.Ile764Asn)
c.1628T>A (p.Ile543Asn)
c.1610T>A (p.Ile537Asn)
n.2705T>A
dbSNP
13g.28018501A>GCA387650198FLT3c.2507T>C (p.Ile836Thr)
c.*419T>C (n.*419T>C)
n.2721T>C
c.2450T>C (p.Ile817Thr)
c.1982T>C (p.Ile661Thr)
c.2291T>C (p.Ile764Thr)
c.1628T>C (p.Ile543Thr)
c.1610T>C (p.Ile537Thr)
n.2705T>C
dbSNP COSMIC

Number of alleles fetched