NM_012452.3(TNFRSF13B):c.542C>A (p.Ala181Glu) AND Common Variable Immune Deficiency, Dominant
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000263268.9
Allele description
NM_012452.3(TNFRSF13B):c.542C>A (p.Ala181Glu)
Condition(s)
- Name:
- Common Variable Immune Deficiency, Dominant
- Identifiers:
- MedGen: CN239265
Assertion and evidence details
Last Updated: Jan 26, 2024