Y78F (p.Tyr78Phe) variant of DNMT1 (P26358)
Y78F (p.Tyr78Phe) in DNMT1 (P26358) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Y78F (p.Tyr78Phe) variant details
- p.Tyr78Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available