Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.128481270G>ACA128572GATA2c.1192C>T (p.Arg398Trp)
c.1474C>T (p.Arg492Trp)
c.167C>T (p.Pro56Leu)
c.1150C>T (p.Arg384Trp)
n.309C>T
ClinVar dbSNP gnomAD v4 COSMIC
3g.128481270G>CCA354413214GATA2c.1192C>G (p.Arg398Gly)
c.1474C>G (p.Arg492Gly)
c.167C>G (p.Pro56Arg)
c.1150C>G (p.Arg384Gly)
n.309C>G
ClinVar dbSNP
3g.128481270G=CA1400714294GATA2c.1192C= (p.Arg398=)
c.1474C= (p.Arg492=)
c.167C= (p.Pro56=)
c.1150C= (p.Arg384=)
n.309C=
dbSNP

Number of alleles fetched