G6D (p.Gly6Asp) variant of NLGN3 (Neuroligin-3)
G6D (p.Gly6Asp) 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.
G6D (p.Gly6Asp) variant details
- p.Gly6Asp
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10070
- NCI-TCGA Cosmic COSV6244
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available