NM_000257.4(MYH7):c.183C>T (p.Ala61=) AND Hypertrophic cardiomyopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000460452.10
Allele description [Variation Report for NM_000257.4(MYH7):c.183C>T (p.Ala61=)]
NM_000257.4(MYH7):c.183C>T (p.Ala61=)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy
- Synonyms:
- HYPERTROPHIC MYOCARDIOPATHY
- Identifiers:
- MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639
-
Homo sapiens zinc finger CCCH-type containing 14 (ZC3H14), transcript variant 14...
Homo sapiens zinc finger CCCH-type containing 14 (ZC3H14), transcript variant 14, mRNAgi|1676440329|ref|NM_001326302.2|Nucleotide
-
Rattus norvegicus cytochrome P450 CYP2B21 mRNA, complete cds
Rattus norvegicus cytochrome P450 CYP2B21 mRNA, complete cdsgi|15826837|gb|AF159245.2|Nucleotide
-
KIRREL2 [Dasypus novemcinctus]
KIRREL2 [Dasypus novemcinctus]Gene ID:105746736Gene
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Last Updated: Sep 29, 2024