NM_005862.3(STAG1):c.3241C>T (p.Arg1081Ter) AND Intellectual disability, autosomal dominant 47
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Dec 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003493272.1
Allele description [Variation Report for NM_005862.3(STAG1):c.3241C>T (p.Arg1081Ter)]
NM_005862.3(STAG1):c.3241C>T (p.Arg1081Ter)
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024