G16V (p.Gly16Val) variant of ANKRD1 (Q15327)
G16V (p.Gly16Val) in ANKRD1 (Q15327) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
G16V (p.Gly16Val) variant details
- p.Gly16Val
- TOPMed rs1847422812
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- UniProt: Uncertain significance
- Structural context available