S69C (p.Ser69Cys) variant of CHRNA4 (P43681)
S69C (p.Ser69Cys) in CHRNA4 (P43681) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S69C (p.Ser69Cys) variant details
- p.Ser69Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.