NM_000744.7(CHRNA4):c.1158C>G (p.Pro386=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 4, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000428571.1
Allele description [Variation Report for NM_000744.7(CHRNA4):c.1158C>G (p.Pro386=)]
NM_000744.7(CHRNA4):c.1158C>G (p.Pro386=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024