NM_006565.4(CTCF):c.1164C>T (p.Ser388=) AND History of neurodevelopmental disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 15, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000715378.2
Allele description
NM_006565.4(CTCF):c.1164C>T (p.Ser388=)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Jun 24, 2022