NM_144573.4(NEXN):c.579A>G (p.Glu193=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 1, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000891702.3
Allele description
NM_144573.4(NEXN):c.579A>G (p.Glu193=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 7, 2023