NM_032415.7(CARD11):c.3113C>T (p.Ala1038Val) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003160258.2
Allele description [Variation Report for NM_032415.7(CARD11):c.3113C>T (p.Ala1038Val)]
NM_032415.7(CARD11):c.3113C>T (p.Ala1038Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024