L20D (p.Leu20Asp) variant of CHD8 (Q9HCK8)
L20D (p.Leu20Asp) in CHD8 (Q9HCK8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
L20D (p.Leu20Asp) variant details
- p.Leu20Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.