NM_001032386.2(SUOX):c.556C>T (p.Leu186=) AND Sulfite oxidase deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003638185.1
Allele description [Variation Report for NM_001032386.2(SUOX):c.556C>T (p.Leu186=)]
NM_001032386.2(SUOX):c.556C>T (p.Leu186=)
Condition(s)
- Name:
- Sulfite oxidase deficiency
- Synonyms:
- Isolated sulfite oxidase deficiency
- Identifiers:
- MONDO: MONDO:0010089; MedGen: C0268624; Orphanet: 833; OMIM: 272300; Human Phenotype Ontology: HP:0003643
Assertion and evidence details
Last Updated: Feb 28, 2024