G116D (p.Gly116Asp) variant of SLC2A1 (P11166)
G116D (p.Gly116Asp) in SLC2A1 (P11166) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
G116D (p.Gly116Asp) variant details
- p.Gly116Asp
- ExAC rs769786931
- gnomAD rs769786931
- Missense
- Variant Prioritization Score for Impact Estimate 0.454
- REVEL 0.52
- CADD 22.30
- PolyPhen-2 0.20
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 4.5e-05)
- Structural context available