D47G (p.Asp47Gly) variant of GRN (Progranulin)
D47G (p.Asp47Gly) in GRN (Progranulin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D47G (p.Asp47Gly) variant details
- p.Asp47Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available