A68T (p.Ala68Thr) variant of GATA2 (P23769)
A68T (p.Ala68Thr) in GATA2 (P23769) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
A68T (p.Ala68Thr) variant details
- p.Ala68Thr
- 1000Genomes rs534541303
- TOPMed rs534541303
- gnomAD rs534541303
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available