NM_000257.4(MYH7):c.297C>T (p.Pro99=) AND Hypertrophic cardiomyopathy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000231766.20
Allele description [Variation Report for NM_000257.4(MYH7):c.297C>T (p.Pro99=)]
NM_000257.4(MYH7):c.297C>T (p.Pro99=)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy
- Synonyms:
- HYPERTROPHIC MYOCARDIOPATHY
- Identifiers:
- MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639
Assertion and evidence details
Last Updated: Nov 24, 2024