NM_001365902.3(NFIX):c.564C>T (p.Ser188=) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002914716.2
Allele description [Variation Report for NM_001365902.3(NFIX):c.564C>T (p.Ser188=)]
NM_001365902.3(NFIX):c.564C>T (p.Ser188=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024