NM_000257.4(MYH7):c.786C>T (p.Asp262=) AND Cardiomyopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001187744.2
Allele description [Variation Report for NM_000257.4(MYH7):c.786C>T (p.Asp262=)]
NM_000257.4(MYH7):c.786C>T (p.Asp262=)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
-
B4GALT7 [Bison bison bison]
B4GALT7 [Bison bison bison]Gene ID:104993320Gene
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Last Updated: Nov 5, 2022