V18A (p.Val18Ala) variant of NLGN3 (Neuroligin-3)
V18A (p.Val18Ala) 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 structural context.
V18A (p.Val18Ala) variant details
- p.Val18Ala
- TOPMed rs1193269621
- gnomAD rs1193269621
- Missense
- Variant Prioritization Score for Impact Estimate 0.182
- REVEL 0.15
- CADD 12.30
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 1.9e-05)
- Structural context available