G116V (p.Gly116Val) variant of SLC2A2 (P11168)
G116V (p.Gly116Val) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.86 / 1. The record also includes population frequency data and structural context.
G116V (p.Gly116Val) variant details
- p.Gly116Val
- ExAC rs768407637
- TOPMed rs768407637
- gnomAD rs768407637
- Missense
- Variant Prioritization Score for Impact Estimate 0.859
- REVEL 0.92
- CADD 25.60
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available