NM_000257.4(MYH7):c.4869T>C (p.Asn1623=) AND Hypertrophic cardiomyopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002063237.5
Allele description [Variation Report for NM_000257.4(MYH7):c.4869T>C (p.Asn1623=)]
NM_000257.4(MYH7):c.4869T>C (p.Asn1623=)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy
- Synonyms:
- HYPERTROPHIC MYOCARDIOPATHY
- Identifiers:
- MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639
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xl11044H06F_1376830 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clon...
xl11044H06F_1376830 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clone xl11044H06 5', mRNA sequencegi|798017101|gnl|dbEST|79648324|gb| 622.1|Nucleotide
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Last Updated: Feb 20, 2024