V38D (p.Val38Asp) variant of PDGFRA (P16234)
V38D (p.Val38Asp) in PDGFRA (P16234) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V38D (p.Val38Asp) variant details
- p.Val38Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available