NM_006282.5(STK4):c.1092A>G (p.Gln364=) AND Combined immunodeficiency due to STK4 deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002785288.2
Allele description [Variation Report for NM_006282.5(STK4):c.1092A>G (p.Gln364=)]
NM_006282.5(STK4):c.1092A>G (p.Gln364=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024