V2F (p.Val2Phe) variant of GRM5 (P41594)
V2F (p.Val2Phe) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data.
V2F (p.Val2Phe) variant details
- p.Val2Phe
- gnomAD rs1366355209
- Missense
- Variant Prioritization Score for Impact Estimate 0.579
- REVEL 0.58
- MetaLR 0.70
- MetaSVM 0.32
- CADD 21.30
- PolyPhen-2 0.06
- SIFT 0.05
- Most common in the East Asian population (allele frequency 2.5e-05)