Q26H (p.Gln26His) variant of SMAD3 (SMAD family member 3)
Q26H (p.Gln26His) in SMAD3 (SMAD family member 3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Q26H (p.Gln26His) variant details
- p.Gln26His
- NCI-TCGA Cosmic COSV5928
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available