P52L (p.Pro52Leu) variant of MOG (Q16653)
P52L (p.Pro52Leu) in MOG (Q16653) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P52L (p.Pro52Leu) variant details
- p.Pro52Leu
- NCI-TCGA TCGA novel
- Ensembl rs1767961042
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available