NM_173728.4(ARHGEF15):c.232C>T (p.Pro78Ser) AND Early infantile epileptic encephalopathy with suppression bursts
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 21, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000699664.8
Allele description [Variation Report for NM_173728.4(ARHGEF15):c.232C>T (p.Pro78Ser)]
NM_173728.4(ARHGEF15):c.232C>T (p.Pro78Ser)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024