NM_001032386.2(SUOX):c.1281G>C (p.Ser427=) AND Sulfite oxidase deficiency
- Germline classification:
- Benign (5 submissions)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000363638.25
Allele description [Variation Report for NM_001032386.2(SUOX):c.1281G>C (p.Ser427=)]
NM_001032386.2(SUOX):c.1281G>C (p.Ser427=)
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: Oct 13, 2024