S39S (p.Ser39Ser) variant of GABRG2 (P18507)
S39S (p.Ser39Ser) in GABRG2 (P18507) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
S39S (p.Ser39Ser) variant details
- p.Ser39Ser
- rs575089001
- gnomAD 5-162036949-C-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0889
- CADD 1.17
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available
- Literature evidence available