V69E (p.Val69Glu) variant of MYH6 (Myosin-6)
V69E (p.Val69Glu) in MYH6 (Myosin-6) 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.
V69E (p.Val69Glu) variant details
- p.Val69Glu
- rs2502209394
- ClinGen CA389031829
- ClinVar RCV002422112
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available