H101R (p.His101Arg) variant of GRM5 (P41594)
H101R (p.His101Arg) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data.
H101R (p.His101Arg) variant details
- p.His101Arg
- TOPMed rs1272209457
- Missense
- Variant Prioritization Score for Impact Estimate 0.459
- REVEL 0.50
- MetaLR 0.20
- MetaSVM -0.70
- CADD 24.80
- PolyPhen-2 0.65
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)