NM_000256.3(MYBPC3):c.1191C>T (p.Leu397=) AND Cardiomyopathy
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Dec 9, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001188575.11
Allele description [Variation Report for NM_000256.3(MYBPC3):c.1191C>T (p.Leu397=)]
NM_000256.3(MYBPC3):c.1191C>T (p.Leu397=)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
Assertion and evidence details
Last Updated: Oct 13, 2024