G148W (p.Gly148Trp) variant of GRM5 (P41594)
G148W (p.Gly148Trp) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.92 / 1. The record also includes population frequency data.
G148W (p.Gly148Trp) variant details
- p.Gly148Trp
- cosmic curated COSV59606
- Ensembl rs2135150965
- Missense
- Variant Prioritization Score for Impact Estimate 0.92
- REVEL 0.98
- MetaLR 0.97
- MetaSVM 1.09
- CADD 27.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)