NM_000626.4(CD79B):c.338G>A (p.Arg113Gln) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004027938.1
Allele description [Variation Report for NM_000626.4(CD79B):c.338G>A (p.Arg113Gln)]
NM_000626.4(CD79B):c.338G>A (p.Arg113Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024