P16H (p.Pro16His) variant of NLGN3 (Neuroligin-3)
P16H (p.Pro16His) in NLGN3 (Neuroligin-3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P16H (p.Pro16His) variant details
- p.Pro16His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.