C79T (p.Cys79Thr) variant of SIRT7 (Q9NRC8)
C79T (p.Cys79Thr) 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.
C79T (p.Cys79Thr) variant details
- p.Cys79Thr
- NCI-TCGA Cosmic COSV6081
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available