P91Q (p.Pro91Gln) variant of NLGN4X (Neuroligin-4, X-linked)
P91Q (p.Pro91Gln) in NLGN4X (Neuroligin-4, X-linked) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
P91Q (p.Pro91Gln) variant details
- p.Pro91Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.74
- MetaSVM 0.69
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available