NM_021072.4(HCN1):c.477C>G (p.Ile159Met) AND Early infantile epileptic encephalopathy with suppression bursts
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001066815.9
Allele description [Variation Report for NM_021072.4(HCN1):c.477C>G (p.Ile159Met)]
NM_021072.4(HCN1):c.477C>G (p.Ile159Met)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024