S59C (p.Ser59Cys) variant of GNA13 (Q14344)
S59C (p.Ser59Cys) in GNA13 (Q14344) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S59C (p.Ser59Cys) variant details
- p.Ser59Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available