D89G (p.Asp89Gly) variant of MYH7 (Myosin-7)
D89G (p.Asp89Gly) in MYH7 (Myosin-7) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hypertrophic cardiomyopathy. The record also includes structural context.
D89G (p.Asp89Gly) variant details
- p.Asp89Gly
- rs2502320216
- ClinGen CA389053299
- ClinVar RCV003749073
- NCI-TCGA TCGA novel
- Uncertain significance
- Hypertrophic cardiomyopathy
- Missense
- ClinVar: Uncertain significance (Hypertrophic cardiomyopathy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available