R61H (p.Arg61His) variant of GRM5 (P41594)
R61H (p.Arg61His) 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 0.56 / 1. The record also includes population frequency data.
R61H (p.Arg61His) variant details
- p.Arg61His
- rs781430828
- NCI-TCGA Cosmic COSV5963
- cosmic curated COSV59630
- ExAC rs781430828
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.563
- REVEL 0.45
- MetaLR 0.48
- MetaSVM -0.18
- CADD 25.80
- PolyPhen-2 0.99
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)