V16I (p.Val16Ile) variant of GRM5 (P41594)
V16I (p.Val16Ile) in GRM5 (P41594) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data.
V16I (p.Val16Ile) variant details
- p.Val16Ile
- gnomAD rs1229855231
- Missense
- Variant Prioritization Score for Impact Estimate 0.481
- REVEL 0.32
- MetaLR 0.65
- MetaSVM -0.23
- CADD 18.40
- PolyPhen-2 0.01
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 9e-07)