P7Q (p.Pro7Gln) variant of NLGN3 (Neuroligin-3)
P7Q (p.Pro7Gln) in NLGN3 (Neuroligin-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data, published literature, and structural context.
P7Q (p.Pro7Gln) variant details
- p.Pro7Gln
- gnomAD X-71147769-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0706
- REVEL 0.07
- CADD 0.59
- PolyPhen-2 0.12
- SIFT 0.36
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available