R97W (p.Arg97Trp) variant of NLGN3 (Neuroligin-3)
R97W (p.Arg97Trp) in NLGN3 (Neuroligin-3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
R97W (p.Arg97Trp) variant details
- p.Arg97Trp
- rs761085827
- ExAC rs761085827
- gnomAD rs761085827
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.662
- REVEL 0.62
- CADD 27.20
- PolyPhen-2 0.98
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.2e-05)
- Structural context available