P90H (p.Pro90His) variant of NLGN4X (Neuroligin-4, X-linked)
P90H (p.Pro90His) in NLGN4X (Neuroligin-4, X-linked) 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 0.56 / 1. The record also includes population frequency data and structural context.
P90H (p.Pro90His) variant details
- p.Pro90His
- rs1199804447
- gnomAD rs1199804447
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.557
- REVEL 0.54
- MetaLR 0.53
- MetaSVM 0.18
- CADD 23.50
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 3.8e-05)
- Structural context available