NM_000257.4(MYH7):c.732+17C>A AND Hypertrophic cardiomyopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002637584.3
Allele description [Variation Report for NM_000257.4(MYH7):c.732+17C>A]
NM_000257.4(MYH7):c.732+17C>A
Condition(s)
- Name:
- Hypertrophic cardiomyopathy
- Synonyms:
- HYPERTROPHIC MYOCARDIOPATHY
- Identifiers:
- MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639
-
Homo sapiens guided entry of tail-anchored proteins factor 4 (GET4), mRNA
Homo sapiens guided entry of tail-anchored proteins factor 4 (GET4), mRNAgi|1519312250|ref|NM_015949.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024