S39T (p.Ser39Thr) variant of GABRG2 (P18507)
S39T (p.Ser39Thr) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
S39T (p.Ser39Thr) variant details
- p.Ser39Thr
- gnomAD 5-162036947-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.12
- CADD 2.27
- SIFT 0.39
- Population evidence available
- Structural context available
- Literature evidence available