NM_144573.4(NEXN):c.1372T>C (p.Leu458=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 18, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001404905.7
Allele description [Variation Report for NM_144573.4(NEXN):c.1372T>C (p.Leu458=)]
NM_144573.4(NEXN):c.1372T>C (p.Leu458=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024