NM_005787.6(ALG3):c.579C>T (p.Arg193=) AND ALG3-congenital disorder of glycosylation
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003022728.2
Allele description [Variation Report for NM_005787.6(ALG3):c.579C>T (p.Arg193=)]
NM_005787.6(ALG3):c.579C>T (p.Arg193=)
Condition(s)
- Name:
- ALG3-congenital disorder of glycosylation
- Synonyms:
- CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG Id; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE IV; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0010998; MedGen: C1832736; Orphanet: 79321; OMIM: 601110
Assertion and evidence details
Last Updated: Feb 20, 2024