S2G (p.Ser2Gly) variant of GABRG2 (P18507)
S2G (p.Ser2Gly) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
S2G (p.Ser2Gly) variant details
- p.Ser2Gly
- ExAC rs747787220
- gnomAD rs747787220
- Missense
- Variant Prioritization Score for Impact Estimate 0.394
- CADD 23.40
- PolyPhen-2 0.00
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available