NM_000784.4(CYP27A1):c.215T>A (p.Leu72Gln) AND not provided
- Germline classification:
- Uncertain significance (4 submissions)
- Last evaluated:
- Oct 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001579919.7
Allele description [Variation Report for NM_000784.4(CYP27A1):c.215T>A (p.Leu72Gln)]
NM_000784.4(CYP27A1):c.215T>A (p.Leu72Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024