D13Y (p.Asp13Tyr) variant of CHD7 (Q9P2D1)
D13Y (p.Asp13Tyr) in CHD7 (Q9P2D1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes experimental measurements and structural context.
D13Y (p.Asp13Tyr) variant details
- p.Asp13Tyr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- CHD7 BRK domain domainome 1.0: score -0.304