NM_006790.3(MYOT):c.1401T>C (p.Asn467=) AND Myofibrillar myopathy 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001078699.11
Allele description [Variation Report for NM_006790.3(MYOT):c.1401T>C (p.Asn467=)]
NM_006790.3(MYOT):c.1401T>C (p.Asn467=)
Condition(s)
- Name:
- Myofibrillar myopathy 3 (MFM3)
- Synonyms:
- Limb-girdle muscular dystrophy, type 1A; Muscular dystrophy, proximal, type 1A; Spheroid body myopathy; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0012215; MedGen: C3714934; Orphanet: 266; Orphanet: 268129; OMIM: 609200
Assertion and evidence details
Last Updated: Oct 20, 2024