NM_000104.4(CYP1B1):c.142C>G (p.Arg48Gly) 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:
- RCV000078125.21
Allele description [Variation Report for NM_000104.4(CYP1B1):c.142C>G (p.Arg48Gly)]
NM_000104.4(CYP1B1):c.142C>G (p.Arg48Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024