NM_001322934.2(NFKB2):c.279G>A (p.Val93=) AND Immunodeficiency, common variable, 10
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002186900.6
Allele description [Variation Report for NM_001322934.2(NFKB2):c.279G>A (p.Val93=)]
NM_001322934.2(NFKB2):c.279G>A (p.Val93=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024