S19R (p.Ser19Arg) variant of GRM5 (P41594)
S19R (p.Ser19Arg) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data.
S19R (p.Ser19Arg) variant details
- p.Ser19Arg
- gnomAD rs1323109091
- Missense
- Variant Prioritization Score for Impact Estimate 0.375
- REVEL 0.48
- MetaLR 0.60
- MetaSVM -0.14
- CADD 15.00
- PolyPhen-2 0.02
- SIFT 0.03
- Most common in the East Asian population (allele frequency 0.0001)