NM_000257.4(MYH7):c.5026C>T (p.Arg1676Trp) AND Cardiomyopathy
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Dec 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001177405.13
Allele description [Variation Report for NM_000257.4(MYH7):c.5026C>T (p.Arg1676Trp)]
NM_000257.4(MYH7):c.5026C>T (p.Arg1676Trp)
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 8, 2024