NM_005159.5(ACTC1):c.456C>T (p.Gly152=) AND Cardiomyopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 3, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001184023.9
Allele description [Variation Report for NM_005159.5(ACTC1):c.456C>T (p.Gly152=)]
NM_005159.5(ACTC1):c.456C>T (p.Gly152=)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
Assertion and evidence details
Last Updated: Nov 24, 2024