NM_000103.4(CYP19A1):c.501C>A (p.Ser167=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000926434.8
Allele description [Variation Report for NM_000103.4(CYP19A1):c.501C>A (p.Ser167=)]
NM_000103.4(CYP19A1):c.501C>A (p.Ser167=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024