NM_001322934.2(NFKB2):c.45T>C (p.Tyr15=) AND Immunodeficiency, common variable, 10
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001394478.14
Allele description [Variation Report for NM_001322934.2(NFKB2):c.45T>C (p.Tyr15=)]
NM_001322934.2(NFKB2):c.45T>C (p.Tyr15=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 24, 2024