P91S (p.Pro91Ser) variant of NLGN4X (Neuroligin-4, X-linked)
P91S (p.Pro91Ser) in NLGN4X (Neuroligin-4, X-linked) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data and structural context.
P91S (p.Pro91Ser) variant details
- p.Pro91Ser
- cosmic curated COSV10877
- Missense
- Variant Prioritization Score for Impact Estimate 0.799
- REVEL 0.92
- MetaLR 0.78
- MetaSVM 0.82
- CADD 23.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available