P37Q (p.Pro37Gln) variant of MOG (Q16653)
P37Q (p.Pro37Gln) 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.
P37Q (p.Pro37Gln) variant details
- p.Pro37Gln
- NCI-TCGA Cosmic COSV1009
- cosmic curated COSV10097
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available