NM_000744.7(CHRNA4):c.1047G>A (p.Leu349=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jun 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003430669.10
Allele description [Variation Report for NM_000744.7(CHRNA4):c.1047G>A (p.Leu349=)]
NM_000744.7(CHRNA4):c.1047G>A (p.Leu349=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024