NM_001100.4(ACTA1):c.990+3G>T AND Actin accumulation myopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002630645.3
Allele description [Variation Report for NM_001100.4(ACTA1):c.990+3G>T]
NM_001100.4(ACTA1):c.990+3G>T
Condition(s)
- Name:
- Actin accumulation myopathy (CMYO2A)
- Synonyms:
- Nemaline myopathy caused by mutation in the alpha-actin gene; CONGENITAL MYOPATHY 2A, TYPICAL, AUTOSOMAL DOMINANT; Myopathy, actin, congenital, with cores; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008070; MedGen: C3711389; OMIM: 161800
-
Acute hepatic steatosis
Acute hepatic steatosisMedGen
-
C4025020[conceptid] (1)
MedGen
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024