F37V (p.Phe37Val) variant of GABRG2 (P18507)
F37V (p.Phe37Val) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
F37V (p.Phe37Val) variant details
- p.Phe37Val
- ExAC rs753427115
- gnomAD rs753427115
- Missense
- Variant Prioritization Score for Impact Estimate 0.443
- CADD 19.40
- PolyPhen-2 0.00
- SIFT 0.55
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available