A131G (p.Ala131Gly) variant of SLC2A2 (P11168)
A131G (p.Ala131Gly) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
A131G (p.Ala131Gly) variant details
- p.Ala131Gly
- TOPMed rs970550665
- gnomAD rs970550665
- Missense
- Variant Prioritization Score for Impact Estimate 0.523
- REVEL 0.36
- CADD 22.50
- PolyPhen-2 0.53
- SIFT 0.47
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available