NM_001077365.2(POMT1):c.1705A>C (p.Ile569Leu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000806701.5
Allele description [Variation Report for NM_001077365.2(POMT1):c.1705A>C (p.Ile569Leu)]
NM_001077365.2(POMT1):c.1705A>C (p.Ile569Leu)
Condition(s)
- Name:
- Autosomal recessive limb-girdle muscular dystrophy type 2K
- Synonyms:
- MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; Limb-girdle muscular dystrophy-dystroglycanopathy, type C1
- Identifiers:
- MONDO: MONDO:0012248; MedGen: C1836373; Orphanet: 86812; OMIM: 609308
- Name:
- Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1 (MDDGB1)
- Synonyms:
- MUSCULAR DYSTROPHY, CONGENITAL, POMT1-RELATED; MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 1
- Identifiers:
- MONDO: MONDO:0013159; MedGen: C5436962; OMIM: 613155
-
Bruinsmia styracoides ATP synthase alpha subunit (atp1) gene, partial cds; mitoc...
Bruinsmia styracoides ATP synthase alpha subunit (atp1) gene, partial cds; mitochondrialgi|57868913|gb|AY725914.1|Nucleotide
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Last Updated: Sep 29, 2024