Y79F (p.Tyr79Phe) variant of DDC (P20711)
Y79F (p.Tyr79Phe) in DDC (P20711) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Y79F (p.Tyr79Phe) variant details
- p.Tyr79Phe
- NCI-TCGA Cosmic COSV6356
- cosmic curated COSV63565
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available