NM_000079.4(CHRNA1):c.1293C>T (p.Leu431=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003884493.7
Allele description [Variation Report for NM_000079.4(CHRNA1):c.1293C>T (p.Leu431=)]
NM_000079.4(CHRNA1):c.1293C>T (p.Leu431=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024