NM_001353921.2(ARHGEF9):c.1452C>T (p.His484=) AND Developmental and epileptic encephalopathy, 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002103767.5
Allele description [Variation Report for NM_001353921.2(ARHGEF9):c.1452C>T (p.His484=)]
NM_001353921.2(ARHGEF9):c.1452C>T (p.His484=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024