NM_006790.3(MYOT):c.149A>G (p.Gln50Arg) AND Myofibrillar myopathy 3
- Germline classification:
- Benign (5 submissions)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000576436.23
Allele description [Variation Report for NM_006790.3(MYOT):c.149A>G (p.Gln50Arg)]
NM_006790.3(MYOT):c.149A>G (p.Gln50Arg)
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
-
unnamed protein product [Albugo candida]
unnamed protein product [Albugo candida]gi|635360496|emb|CCI50233.1|Protein
-
ugt1a5 UDP glucuronosyltransferase 1 family, polypeptide A5 [Danio rerio]
ugt1a5 UDP glucuronosyltransferase 1 family, polypeptide A5 [Danio rerio]Gene ID:100384897Gene
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024