D97N (p.Asp97Asn) variant of SMAD2 (SMAD family member 2)
D97N (p.Asp97Asn) in SMAD2 (SMAD family member 2) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
D97N (p.Asp97Asn) variant details
- p.Asp97Asn
- Ensembl rs2144384343
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available