Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.34880598G>TCA248628RUNX1c.467C>A (p.Ala156Glu)
c.386C>A (p.Ala129Glu)
c.431C>A (p.Ala144Glu)
c.*57C>A (n.*57C>A)
c.428C>A (p.Ala143Glu)
n.646C>A
c.314C>A (p.Ala105Glu)
n.693C>A
ClinVar dbSNP
21g.34880598G>ACA410202550RUNX1c.467C>T (p.Ala156Val)
c.386C>T (p.Ala129Val)
c.431C>T (p.Ala144Val)
c.*57C>T (n.*57C>T)
c.428C>T (p.Ala143Val)
n.646C>T
c.314C>T (p.Ala105Val)
n.693C>T
dbSNP
21g.34880598G>CCA410202551RUNX1c.467C>G (p.Ala156Gly)
c.386C>G (p.Ala129Gly)
c.431C>G (p.Ala144Gly)
c.*57C>G (n.*57C>G)
c.428C>G (p.Ala143Gly)
n.646C>G
c.314C>G (p.Ala105Gly)
n.693C>G
dbSNP

Number of alleles fetched