V19F (p.Val19Phe) variant of NLGN4X (Neuroligin-4, X-linked)
V19F (p.Val19Phe) in NLGN4X (Neuroligin-4, X-linked) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V19F (p.Val19Phe) variant details
- p.Val19Phe
- NCI-TCGA Cosmic COSV9932
- cosmic curated COSV99321
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available