N71D (p.Asn71Asp) variant of SMAD2 (SMAD family member 2)
N71D (p.Asn71Asp) 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.
N71D (p.Asn71Asp) variant details
- p.Asn71Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available