NM_001904.4(CTNNB1):c.283C>T (p.Arg95Ter) AND Inborn genetic diseases
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Nov 6, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000624646.2
Allele description [Variation Report for NM_001904.4(CTNNB1):c.283C>T (p.Arg95Ter)]
NM_001904.4(CTNNB1):c.283C>T (p.Arg95Ter)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Mar 10, 2024