NM_005159.5(ACTC1):c.40A>G (p.Asn14Asp) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003815494.1
Allele description [Variation Report for NM_005159.5(ACTC1):c.40A>G (p.Asn14Asp)]
NM_005159.5(ACTC1):c.40A>G (p.Asn14Asp)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy 11
- Synonyms:
- Familial hypertrophic cardiomyopathy 11; ACTC1-Related Familial Hypertrophic Cardiomyopathy
- Identifiers:
- MONDO: MONDO:0012799; MedGen: C2677506; OMIM: 612098
Assertion and evidence details
Last Updated: Mar 5, 2024