NM_000106.6(CYP2D6):c.886C>T (p.Arg296Cys) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 27, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000616933.2
Allele description
NM_000106.6(CYP2D6):c.886C>T (p.Arg296Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 26, 2023