NM_016203.4(PRKAG2):c.1102G>T (p.Ala368Ser) AND Hypertrophic cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004006496.2
Allele description [Variation Report for NM_016203.4(PRKAG2):c.1102G>T (p.Ala368Ser)]
NM_016203.4(PRKAG2):c.1102G>T (p.Ala368Ser)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy
- Synonyms:
- HYPERTROPHIC MYOCARDIOPATHY
- Identifiers:
- MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639
Assertion and evidence details
Last Updated: Sep 29, 2024