W17C (p.Trp17Cys) variant of REN (Renin)
W17C (p.Trp17Cys) in REN (Renin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
W17C (p.Trp17Cys) variant details
- p.Trp17Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available