Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.28018502T>CCA16603129FLT3c.2506A>G (p.Ile836Val)
c.*418A>G (n.*418A>G)
n.2720A>G
c.2449A>G (p.Ile817Val)
c.1981A>G (p.Ile661Val)
c.2290A>G (p.Ile764Val)
c.1627A>G (p.Ile543Val)
c.1609A>G (p.Ile537Val)
n.2704A>G
ClinVar dbSNP
13g.28018502T>GCA16602447FLT3c.2506A>C (p.Ile836Leu)
c.*418A>C (n.*418A>C)
n.2720A>C
c.2449A>C (p.Ile817Leu)
c.1981A>C (p.Ile661Leu)
c.2290A>C (p.Ile764Leu)
c.1627A>C (p.Ile543Leu)
c.1609A>C (p.Ile537Leu)
n.2704A>C
ClinVar dbSNP COSMIC
13g.28018502T>ACA16603131FLT3c.2506A>T (p.Ile836Phe)
c.*418A>T (n.*418A>T)
n.2720A>T
c.2449A>T (p.Ile817Phe)
c.1981A>T (p.Ile661Phe)
c.2290A>T (p.Ile764Phe)
c.1627A>T (p.Ile543Phe)
c.1609A>T (p.Ile537Phe)
n.2704A>T
ClinVar dbSNP

Number of alleles fetched