P37S (p.Pro37Ser) variant of MOG (Q16653)
P37S (p.Pro37Ser) in MOG (Q16653) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
P37S (p.Pro37Ser) variant details
- p.Pro37Ser
- rs1450240079
- gnomAD rs1450240079
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.408
- AlphaMissense 0.27
- MetaLR 0.33
- MetaSVM -0.37
- PolyPhen-2 0.99
- SIFT 0.02
- EVE 0.20
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available