NM_001353921.2(ARHGEF9):c.1420T>C (p.Ser474Pro) AND Developmental and epileptic encephalopathy, 8
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000543215.6
Allele description [Variation Report for NM_001353921.2(ARHGEF9):c.1420T>C (p.Ser474Pro)]
NM_001353921.2(ARHGEF9):c.1420T>C (p.Ser474Pro)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024