S82C (p.Ser82Cys) variant of SMAD2 (SMAD family member 2)
S82C (p.Ser82Cys) 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.
S82C (p.Ser82Cys) variant details
- p.Ser82Cys
- NCI-TCGA Cosmic COSV5099
- cosmic curated COSV50997
- Ensembl rs2144384859
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available