NM_001330260.2(SCN8A):c.4235T>C (p.Phe1412Ser) AND Developmental and epileptic encephalopathy, 13
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 20, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001330491.2
Allele description [Variation Report for NM_001330260.2(SCN8A):c.4235T>C (p.Phe1412Ser)]
NM_001330260.2(SCN8A):c.4235T>C (p.Phe1412Ser)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024