A32G (p.Ala32Gly) variant of APOL1 (Apolipoprotein L1)
A32G (p.Ala32Gly) in APOL1 (Apolipoprotein L1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
A32G (p.Ala32Gly) variant details
- p.Ala32Gly
- ExAC rs753380461
- TOPMed rs753380461
- gnomAD rs753380461
- Missense
- Variant Prioritization Score for Impact Estimate 0.0593
- REVEL 0.06
- CADD 0.00
- PolyPhen-2 0.02
- SIFT 0.31
- Most common in the Finnish in Finland (FIN) population (allele frequency 7.5e-05)
- Structural context available