P78R (p.Pro78Arg) variant of NLGN3 (Neuroligin-3)
P78R (p.Pro78Arg) in NLGN3 (Neuroligin-3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
P78R (p.Pro78Arg) variant details
- p.Pro78Arg
- NCI-TCGA Cosmic COSV6244
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available