NM_000432.4(MYL2):c.501G>A (p.Ter167=) AND Hypertrophic cardiomyopathy 10
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 25, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002090285.5
Allele description [Variation Report for NM_000432.4(MYL2):c.501G>A (p.Ter167=)]
NM_000432.4(MYL2):c.501G>A (p.Ter167=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024