Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.28027222A>CCA16602564FLT3c.2073T>G (p.Phe691Leu)
n.2155T>G
c.2016T>G (p.Phe672Leu)
c.1548T>G (p.Phe516Leu)
c.1857T>G (p.Phe619Leu)
c.1194T>G (p.Phe398Leu)
c.1176T>G (p.Phe392Leu)
n.2139T>G
ClinVar dbSNP gnomAD v4 COSMIC
13g.28027222A>TCA16602565FLT3c.2073T>A (p.Phe691Leu)
n.2155T>A
c.2016T>A (p.Phe672Leu)
c.1548T>A (p.Phe516Leu)
c.1857T>A (p.Phe619Leu)
c.1194T>A (p.Phe398Leu)
c.1176T>A (p.Phe392Leu)
n.2139T>A
ClinVar dbSNP

Number of alleles fetched