NM_001330260.2(SCN8A):c.5943GAG[1] (p.Ter1981=) AND Early Infantile Epileptic Encephalopathy, Autosomal Dominant
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000359420.13
Allele description [Variation Report for NM_001330260.2(SCN8A):c.5943GAG[1] (p.Ter1981=)]
NM_001330260.2(SCN8A):c.5943GAG[1] (p.Ter1981=)
Condition(s)
- Name:
- Early Infantile Epileptic Encephalopathy, Autosomal Dominant
- Identifiers:
- MedGen: CN239232
-
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Last Updated: Oct 8, 2024