L29F (p.Leu29Phe) variant of NLGN3 (Neuroligin-3)
L29F (p.Leu29Phe) in NLGN3 (Neuroligin-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
L29F (p.Leu29Phe) variant details
- p.Leu29Phe
- gnomAD rs1197857679
- Missense
- Variant Prioritization Score for Impact Estimate 0.225
- REVEL 0.09
- CADD 20.40
- PolyPhen-2 0.11
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 7.1e-06)
- Structural context available