D97A (p.Asp97Ala) variant of SMAD2 (SMAD family member 2)
D97A (p.Asp97Ala) in SMAD2 (SMAD family member 2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D97A (p.Asp97Ala) variant details
- p.Asp97Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available