NM_005263.5(GFI1):c.79C>T (p.Leu27Phe) AND Neutropenia, severe congenital, 2, autosomal dominant
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jan 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001298514.9
Allele description [Variation Report for NM_005263.5(GFI1):c.79C>T (p.Leu27Phe)]
NM_005263.5(GFI1):c.79C>T (p.Leu27Phe)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024