P69L (p.Pro69Leu) variant of NLGN4X (Neuroligin-4, X-linked)
P69L (p.Pro69Leu) in NLGN4X (Neuroligin-4, X-linked) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data and structural context.
P69L (p.Pro69Leu) variant details
- p.Pro69Leu
- gnomAD rs1355781670
- Missense
- Variant Prioritization Score for Impact Estimate 0.586
- REVEL 0.62
- MetaLR 0.46
- MetaSVM -0.00
- CADD 23.90
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 2.8e-05)
- Structural context available