F37L (p.Phe37Leu) variant of MYL3 (Myosin light chain 3)
F37L (p.Phe37Leu) in MYL3 (Myosin light chain 3) 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.
F37L (p.Phe37Leu) variant details
- p.Phe37Leu
- cosmic curated COSV99439
- Ensembl rs2106914309
- Uncertain significance
- Hypertrophic cardiomyopathy
- Missense
- ClinVar: Uncertain significance (Hypertrophic cardiomyopathy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available