NM_021072.4(HCN1):c.1655G>C (p.Ser552Thr) AND Early infantile epileptic encephalopathy with suppression bursts
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001207378.7
Allele description [Variation Report for NM_021072.4(HCN1):c.1655G>C (p.Ser552Thr)]
NM_021072.4(HCN1):c.1655G>C (p.Ser552Thr)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024