G16C (p.Gly16Cys) variant of CHD8 (Q9HCK8)
G16C (p.Gly16Cys) in CHD8 (Q9HCK8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G16C (p.Gly16Cys) variant details
- p.Gly16Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.