Q63H (p.Gln63His) variant of GRM5 (P41594)
Q63H (p.Gln63His) in GRM5 (P41594) is a missense change. Clinical records from EBI and UniProt describe it as benign. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data.
Q63H (p.Gln63His) variant details
- p.Gln63His
- 1000Genomes rs79165784
- ESP rs79165784
- ExAC rs79165784
- TOPMed rs79165784
- Benign
- Missense
- Variant Prioritization Score for Impact Estimate 0.448
- REVEL 0.52
- MetaLR 0.49
- MetaSVM -0.10
- CADD 23.50
- PolyPhen-2 0.98
- SIFT 0.00
- EBI: Benign
- UniProt: Benign
- Most common in the Non-Finnish European population (allele frequency 9e-07)