D131G (p.Asp131Gly) variant of GRM5 (P41594)
D131G (p.Asp131Gly) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data.
D131G (p.Asp131Gly) variant details
- p.Asp131Gly
- gnomAD rs1482344412
- Missense
- Variant Prioritization Score for Impact Estimate 0.528
- REVEL 0.52
- MetaLR 0.50
- MetaSVM -0.04
- CADD 22.60
- PolyPhen-2 0.03
- SIFT 0.03
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.7e-05)