G116A (p.Gly116Ala) variant of SLC2A2 (P11168)
G116A (p.Gly116Ala) in SLC2A2 (P11168) is a missense change. The record also includes structural context.
G116A (p.Gly116Ala) variant details
- p.Gly116Ala
- ExAC rs768407637
- TOPMed rs768407637
- gnomAD rs768407637
- Missense
- Structural context available