S41N (p.Ser41Asn) variant of NLGN4X (Neuroligin-4, X-linked)
S41N (p.Ser41Asn) in NLGN4X (Neuroligin-4, X-linked) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of NLGN4X-related disorder. The record also includes structural context.
S41N (p.Ser41Asn) variant details
- p.Ser41Asn
- rs2519423008
- ClinGen CA412015422
- ClinVar RCV003399539
- Uncertain significance
- NLGN4X-related disorder
- Missense
- ClinVar: Uncertain significance (NLGN4X-related disorder)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available