NM_001191061.2(SLC25A22):c.500G>A (p.Arg167Gln) AND Early infantile epileptic encephalopathy with suppression bursts
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001083871.15
Allele description [Variation Report for NM_001191061.2(SLC25A22):c.500G>A (p.Arg167Gln)]
NM_001191061.2(SLC25A22):c.500G>A (p.Arg167Gln)
Condition(s)
Assertion and evidence details
Last Updated: Apr 20, 2024