NM_001365902.3(NFIX):c.1179C>T (p.His393=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003000126.2
Allele description [Variation Report for NM_001365902.3(NFIX):c.1179C>T (p.His393=)]
NM_001365902.3(NFIX):c.1179C>T (p.His393=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024