V9I (p.Val9Ile) variant of GRM5 (P41594)
V9I (p.Val9Ile) 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 0.33 / 1. The record also includes population frequency data.
V9I (p.Val9Ile) variant details
- p.Val9Ile
- rs778784135
- ExAC rs778784135
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.329
- REVEL 0.21
- MetaLR 0.53
- MetaSVM -0.61
- CADD 13.40
- PolyPhen-2 0.00
- SIFT 0.42
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 2.3e-05)