V28M (p.Val28Met) variant of GRM5 (P41594)
V28M (p.Val28Met) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data.
V28M (p.Val28Met) variant details
- p.Val28Met
- ExAC rs764553864
- gnomAD rs764553864
- Missense
- Variant Prioritization Score for Impact Estimate 0.573
- REVEL 0.40
- MetaLR 0.74
- MetaSVM 0.45
- CADD 23.70
- PolyPhen-2 0.51
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)