A68G (p.Ala68Gly) variant of ANKRD1 (Q15327)
A68G (p.Ala68Gly) in ANKRD1 (Q15327) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
A68G (p.Ala68Gly) variant details
- p.Ala68Gly
- rs2492962490
- ClinGen CA377553248
- ClinVar RCV004120701
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available