NM_144573.4(NEXN):c.1739G>A (p.Gly580Glu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000822424.4
Allele description [Variation Report for NM_144573.4(NEXN):c.1739G>A (p.Gly580Glu)]
NM_144573.4(NEXN):c.1739G>A (p.Gly580Glu)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024