R37G (p.Arg37Gly) variant of F10 (Coagulation factor X)
R37G (p.Arg37Gly) in F10 (Coagulation factor X) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R37G (p.Arg37Gly) variant details
- p.Arg37Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available