S39P (p.Ser39Pro) variant of GABRG2 (P18507)
S39P (p.Ser39Pro) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
S39P (p.Ser39Pro) variant details
- p.Ser39Pro
- rs949992069
- gnomAD 5-162036947-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.159
- CADD 8.15
- SIFT 0.20
- Population evidence available
- Structural context available
- Literature evidence available