C79A (p.Cys79Ala) variant of SIRT7 (Q9NRC8)
C79A (p.Cys79Ala) in SIRT7 (Q9NRC8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C79A (p.Cys79Ala) variant details
- p.Cys79Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available