NM_014141.6(CNTNAP2):c.1581C>T (p.Asp527=) AND History of neurodevelopmental disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 21, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000719997.1
Allele description
NM_014141.6(CNTNAP2):c.1581C>T (p.Asp527=)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Aug 23, 2022