NM_000626.4(CD79B):c.498G>A (p.Thr166=) AND Agammaglobulinemia 6, autosomal recessive
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001407040.7
Allele description [Variation Report for NM_000626.4(CD79B):c.498G>A (p.Thr166=)]
NM_000626.4(CD79B):c.498G>A (p.Thr166=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024