NM_005263.5(GFI1):c.200G>A (p.Arg67Lys) AND Neutropenia, severe congenital, 2, autosomal dominant
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001464891.7
Allele description [Variation Report for NM_005263.5(GFI1):c.200G>A (p.Arg67Lys)]
NM_005263.5(GFI1):c.200G>A (p.Arg67Lys)
Condition(s)
Assertion and evidence details
Last Updated: Jun 2, 2024