NM_144573.4(NEXN):c.1112C>A (p.Pro371Gln) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002582140.1
Allele description [Variation Report for NM_144573.4(NEXN):c.1112C>A (p.Pro371Gln)]
NM_144573.4(NEXN):c.1112C>A (p.Pro371Gln)
Condition(s)
Assertion and evidence details
Last Updated: Feb 13, 2023