NM_000274.4(OAT):c.582C>G (p.Tyr194Ter) AND Ornithine aminotransferase deficiency
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- May 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003471625.1
Allele description [Variation Report for NM_000274.4(OAT):c.582C>G (p.Tyr194Ter)]
NM_000274.4(OAT):c.582C>G (p.Tyr194Ter)
Condition(s)
- Name:
- Ornithine aminotransferase deficiency (GACR)
- Synonyms:
- OAT deficiency; Ornithine ketoacid aminotransferase deficiency; Gyrate atrophy; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009796; MedGen: C0018425; Orphanet: 414; OMIM: 258870
Assertion and evidence details
Last Updated: Dec 30, 2023