P32L (p.Pro32Leu) variant of GRM5 (P41594)
P32L (p.Pro32Leu) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data.
P32L (p.Pro32Leu) variant details
- p.Pro32Leu
- rs1287949065
- cosmic curated COSV59588
- gnomAD rs1287949065
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.566
- REVEL 0.45
- MetaLR 0.62
- MetaSVM 0.20
- CADD 22.70
- PolyPhen-2 0.24
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available