S79F (p.Ser79Phe) variant of UNC13D (Protein unc-13 homolog D)
S79F (p.Ser79Phe) in UNC13D (Protein unc-13 homolog D) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S79F (p.Ser79Phe) variant details
- p.Ser79Phe
- NCI-TCGA Cosmic COSV5288
- cosmic curated COSV52884
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available