NM_001194998.2(CEP152):c.4072C>G (p.Gln1358Glu) AND Seckel syndrome 5
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000381261.6
Allele description [Variation Report for NM_001194998.2(CEP152):c.4072C>G (p.Gln1358Glu)]
NM_001194998.2(CEP152):c.4072C>G (p.Gln1358Glu)
Condition(s)
Assertion and evidence details
Last Updated: Oct 26, 2024