S39F (p.Ser39Phe) variant of GABRG2 (P18507)
S39F (p.Ser39Phe) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
S39F (p.Ser39Phe) variant details
- p.Ser39Phe
- gnomAD 5-162036948-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.145
- CADD 2.79
- SIFT 0.66
- Population evidence available
- Structural context available
- Literature evidence available