D11H (p.Asp11His) variant of DNMT3A (Q9Y6K1)
D11H (p.Asp11His) in DNMT3A (Q9Y6K1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
D11H (p.Asp11His) variant details
- p.Asp11His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available