R52M (p.Arg52Met) variant of NLGN3 (Neuroligin-3)
R52M (p.Arg52Met) in NLGN3 (Neuroligin-3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R52M (p.Arg52Met) variant details
- p.Arg52Met
- NCI-TCGA Cosmic COSV6244
- cosmic curated COSV62444
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available