NM_002163.4(IRF8):c.1086C>A (p.Ser362=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003794558.1
Allele description [Variation Report for NM_002163.4(IRF8):c.1086C>A (p.Ser362=)]
NM_002163.4(IRF8):c.1086C>A (p.Ser362=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024