NM_001194998.2(CEP152):c.3727C>G (p.Pro1243Ala) AND Microcephaly 9, primary, autosomal recessive
- Germline classification:
- Uncertain significance (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:
- RCV001117855.4
Allele description [Variation Report for NM_001194998.2(CEP152):c.3727C>G (p.Pro1243Ala)]
NM_001194998.2(CEP152):c.3727C>G (p.Pro1243Ala)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023