S10C (p.Ser10Cys) variant of NPR1 (P16066)
S10C (p.Ser10Cys) in NPR1 (P16066) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S10C (p.Ser10Cys) variant details
- p.Ser10Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available