Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.128485741G>CCA354405115GATA2c.857C>G (p.Ala286Gly)
c.1139C>G (p.Ala380Gly)
ClinVar dbSNP
3g.128485741G>ACA207231GATA2c.857C>T (p.Ala286Val)
c.1139C>T (p.Ala380Val)
ClinVar dbSNP
3g.128485741G=CA1400718892GATA2c.857C= (p.Ala286=)
c.1139C= (p.Ala380=)
dbSNP
3g.128485741G>TCA354405116GATA2c.857C>A (p.Ala286Asp)
c.1139C>A (p.Ala380Asp)
dbSNP gnomAD v4

Number of alleles fetched