NM_001330260.2(SCN8A):c.5466C>T (p.Pro1822=) AND Early infantile epileptic encephalopathy with suppression bursts
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002215070.6
Allele description [Variation Report for NM_001330260.2(SCN8A):c.5466C>T (p.Pro1822=)]
NM_001330260.2(SCN8A):c.5466C>T (p.Pro1822=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024