L79P (p.Leu79Pro) variant of DNMT1 (P26358)
L79P (p.Leu79Pro) 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.
L79P (p.Leu79Pro) variant details
- p.Leu79Pro
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10053
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available