NM_000497.4(CYP11B1):c.369T>C (p.Arg123=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000936782.7
Allele description [Variation Report for NM_000497.4(CYP11B1):c.369T>C (p.Arg123=)]
NM_000497.4(CYP11B1):c.369T>C (p.Arg123=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024