A59T (p.Ala59Thr) variant of GRM5 (P41594)
A59T (p.Ala59Thr) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data.
A59T (p.Ala59Thr) variant details
- p.Ala59Thr
- TOPMed rs1941671193
- Missense
- Variant Prioritization Score for Impact Estimate 0.362
- REVEL 0.12
- MetaLR 0.22
- MetaSVM -0.75
- CADD 23.00
- PolyPhen-2 0.23
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)