A16G (p.Ala16Gly) variant of CYP21A2 (Steroid 21-hydroxylase)
A16G (p.Ala16Gly) in CYP21A2 (Steroid 21-hydroxylase) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance in the context of in AH3. The record also includes structural context.
A16G (p.Ala16Gly) variant details
- p.Ala16Gly
- gnomAD rs1350215986
- Uncertain significance
- in AH3
- Missense
- EBI: uncertain significance (in AH3)
- UniProt: Uncertain significance (in AH3)
- Structural context available