V18F (p.Val18Phe) variant of NLGN3 (Neuroligin-3)
V18F (p.Val18Phe) in NLGN3 (Neuroligin-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
V18F (p.Val18Phe) variant details
- p.Val18Phe
- gnomAD X-71147801-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.275
- REVEL 0.26
- CADD 10.70
- PolyPhen-2 0.00
- SIFT 0.61
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available