G68V (p.Gly68Val) variant of NLGN4X (Neuroligin-4, X-linked)
G68V (p.Gly68Val) 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 0.47 / 1. The record also includes population frequency data and structural context.
G68V (p.Gly68Val) variant details
- p.Gly68Val
- NCI-TCGA Cosmic COSV9931
- cosmic curated COSV99319
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.471
- REVEL 0.41
- MetaLR 0.38
- MetaSVM -0.25
- CADD 21.00
- 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-06)
- Structural context available