A39P (p.Ala39Pro) variant of GRM5 (P41594)
A39P (p.Ala39Pro) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.85 / 1. The record also includes population frequency data.
A39P (p.Ala39Pro) variant details
- p.Ala39Pro
- Ensembl rs1565351102
- Missense
- Variant Prioritization Score for Impact Estimate 0.848
- REVEL 0.91
- MetaLR 0.80
- MetaSVM 0.63
- CADD 25.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)