NM_001330260.2(SCN8A):c.666C>T (p.Phe222=) AND Early infantile epileptic encephalopathy with suppression bursts
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002212470.7
Allele description [Variation Report for NM_001330260.2(SCN8A):c.666C>T (p.Phe222=)]
NM_001330260.2(SCN8A):c.666C>T (p.Phe222=)
Condition(s)
-
Homo sapiens zinc finger protein 689 (ZNF689), transcript variant 2, non-coding ...
Homo sapiens zinc finger protein 689 (ZNF689), transcript variant 2, non-coding RNAgi|1676452926|ref|NR_073480.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024