Q78H (p.Gln78His) variant of MYH6 (Myosin-6)
Q78H (p.Gln78His) 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.
Q78H (p.Gln78His) variant details
- p.Gln78His
- rs1891766127
- ClinGen CA389031769
- ClinVar RCV004136868
- gnomAD rs1891766127
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available