D41H (p.Asp41His) variant of MYH6 (Myosin-6)
D41H (p.Asp41His) 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.
D41H (p.Asp41His) variant details
- p.Asp41His
- rs201161721
- ClinGen CA389032031
- ClinVar RCV004452498
- NCI-TCGA TCGA novel
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available