S2W (p.Ser2Trp) variant of SMAD2 (SMAD family member 2)
S2W (p.Ser2Trp) 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.
S2W (p.Ser2Trp) variant details
- p.Ser2Trp
- NCI-TCGA Cosmic COSV1000
- NCI-TCGA Cosmic COSV5099
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available