NM_002485.5(NBN):c.1563C>T (p.Asn521=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 26, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001697387.9
Allele description [Variation Report for NM_002485.5(NBN):c.1563C>T (p.Asn521=)]
NM_002485.5(NBN):c.1563C>T (p.Asn521=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 26, 2024