NM_000257.4(MYH7):c.3193A>G (p.Ser1065Gly) AND Cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004012688.2
Allele description [Variation Report for NM_000257.4(MYH7):c.3193A>G (p.Ser1065Gly)]
NM_000257.4(MYH7):c.3193A>G (p.Ser1065Gly)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
Assertion and evidence details
Last Updated: May 7, 2024