S9S (p.Ser9Ser) variant of NLGN3 (Neuroligin-3)
S9S (p.Ser9Ser) in NLGN3 (Neuroligin-3) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and published literature.
S9S (p.Ser9Ser) variant details
- p.Ser9Ser
- rs781426057
- gnomAD X-71147776-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.232
- CADD 8.43
- Most common in the African/African-American population (allele frequency 0.00016)
- Literature evidence available