N109S (p.Asn109Ser) variant of NLGN3 (Neuroligin-3)
N109S (p.Asn109Ser) in NLGN3 (Neuroligin-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
N109S (p.Asn109Ser) variant details
- p.Asn109Ser
- ExAC rs763800070
- gnomAD rs763800070
- Missense
- Variant Prioritization Score for Impact Estimate 0.263
- REVEL 0.09
- CADD 18.70
- PolyPhen-2 0.03
- SIFT 0.45
- Most common in the South Asian population (allele frequency 1.8e-05)
- Structural context available