NM_001556.3(IKBKB):c.477+7G>A AND Severe combined immunodeficiency due to IKK2 deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003053169.2
Allele description [Variation Report for NM_001556.3(IKBKB):c.477+7G>A]
NM_001556.3(IKBKB):c.477+7G>A
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024