A64V (p.Ala64Val) variant of SMAD2 (SMAD family member 2)
A64V (p.Ala64Val) 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.
A64V (p.Ala64Val) variant details
- p.Ala64Val
- NCI-TCGA TCGA novel
- Ensembl rs2144474353
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available