F137Y (p.Phe137Tyr) variant of GRM5 (P41594)
F137Y (p.Phe137Tyr) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data.
F137Y (p.Phe137Tyr) variant details
- p.Phe137Tyr
- 1000Genomes rs72954992
- ExAC rs72954992
- gnomAD rs72954992
- Missense
- Variant Prioritization Score for Impact Estimate 0.339
- REVEL 0.31
- MetaLR 0.34
- MetaSVM -0.25
- CADD 19.30
- PolyPhen-2 0.23
- SIFT 0.10
- Most common in the South Asian population (allele frequency 1.2e-05)