NM_000104.4(CYP1B1):c.355G>T (p.Ala119Ser) AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Dec 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000078127.21
Allele description [Variation Report for NM_000104.4(CYP1B1):c.355G>T (p.Ala119Ser)]
NM_000104.4(CYP1B1):c.355G>T (p.Ala119Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024