G17C (p.Gly17Cys) variant of GNA13 (Q14344)
G17C (p.Gly17Cys) in GNA13 (Q14344) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not specified.
G17C (p.Gly17Cys) variant details
- p.Gly17Cys
- TOPMed rs1421154389
- gnomAD rs1421154389
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance