P16S (p.Pro16Ser) variant of NLGN3 (Neuroligin-3)
P16S (p.Pro16Ser) in NLGN3 (Neuroligin-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and published literature.
P16S (p.Pro16Ser) variant details
- p.Pro16Ser
- gnomAD X-71147795-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.184
- REVEL 0.03
- CADD 8.36
- PolyPhen-2 0.00
- SIFT 0.55
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Literature evidence available