V52I (p.Val52Ile) variant of GRM5 (P41594)
V52I (p.Val52Ile) 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 0.55 / 1. The record also includes population frequency data.
V52I (p.Val52Ile) variant details
- p.Val52Ile
- NCI-TCGA Cosmic COSV5960
- cosmic curated COSV59607
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.554
- REVEL 0.38
- MetaLR 0.71
- MetaSVM 0.34
- CADD 23.30
- PolyPhen-2 0.86
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)