D78G (p.Asp78Gly) variant of CARD11 (Q9BXL7)
D78G (p.Asp78Gly) in CARD11 (Q9BXL7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D78G (p.Asp78Gly) variant details
- p.Asp78Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available