S82P (p.Ser82Pro) variant of SMAD2 (SMAD family member 2)
S82P (p.Ser82Pro) in SMAD2 (SMAD family member 2) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
S82P (p.Ser82Pro) variant details
- p.Ser82Pro
- rs2511354421
- ClinGen CA402502449
- ClinVar RCV003568809
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available