NM_000232.5(SGCB):c.151C>T (p.Arg51Cys) AND Autosomal recessive limb-girdle muscular dystrophy type 2E
- Germline classification:
- Uncertain significance (4 submissions)
- Last evaluated:
- Oct 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000697786.17
Allele description [Variation Report for NM_000232.5(SGCB):c.151C>T (p.Arg51Cys)]
NM_000232.5(SGCB):c.151C>T (p.Arg51Cys)
Condition(s)
- Name:
- Autosomal recessive limb-girdle muscular dystrophy type 2E (LGMDR4)
- Synonyms:
- Limb-girdle muscular dystrophy, type 2E; Muscular dystrophy limb-girdle with beta-sarcoglycan deficiency; Beta-sarcoglycan limb-girdle muscular dystrophy; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011423; MedGen: C1858593; Orphanet: 119; OMIM: 604286
Assertion and evidence details
Last Updated: Oct 8, 2024