NM_001165963.4(SCN1A):c.1377+20T>C AND Early infantile epileptic encephalopathy with suppression bursts
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 18, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002122278.6
Allele description [Variation Report for NM_001165963.4(SCN1A):c.1377+20T>C]
NM_001165963.4(SCN1A):c.1377+20T>C
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024