A38D (p.Ala38Asp) variant of SPTBN4 (Q9H254)
A38D (p.Ala38Asp) in SPTBN4 (Q9H254) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A38D (p.Ala38Asp) variant details
- p.Ala38Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available