V56I (p.Val56Ile) variant of NLGN3 (Neuroligin-3)
V56I (p.Val56Ile) in NLGN3 (Neuroligin-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
V56I (p.Val56Ile) variant details
- p.Val56Ile
- ExAC rs752463312
- gnomAD rs752463312
- Missense
- Variant Prioritization Score for Impact Estimate 0.385
- REVEL 0.19
- CADD 21.30
- PolyPhen-2 0.29
- SIFT 0.18
- Most common in the South Asian population (allele frequency 1.9e-05)
- Structural context available