NM_001322934.2(NFKB2):c.66C>T (p.Ser22=) AND Immunodeficiency, common variable, 10
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 11, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001423795.8
Allele description [Variation Report for NM_001322934.2(NFKB2):c.66C>T (p.Ser22=)]
NM_001322934.2(NFKB2):c.66C>T (p.Ser22=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024