NM_012452.3(TNFRSF13B):c.41G>A (p.Arg14His) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001811468.13
Allele description [Variation Report for NM_012452.3(TNFRSF13B):c.41G>A (p.Arg14His)]
NM_012452.3(TNFRSF13B):c.41G>A (p.Arg14His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024