NM_000744.7(CHRNA4):c.858C>T (p.Thr286=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 28, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000420019.1
Allele description
NM_000744.7(CHRNA4):c.858C>T (p.Thr286=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 8, 2021