NM_000498.3(CYP11B2):c.1353C>T (p.Leu451=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000917179.9
Allele description [Variation Report for NM_000498.3(CYP11B2):c.1353C>T (p.Leu451=)]
NM_000498.3(CYP11B2):c.1353C>T (p.Leu451=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024