NM_001008537.3(NEXMIF):c.151C>A (p.Pro51Thr) AND History of neurodevelopmental disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 24, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000715971.2
Allele description
NM_001008537.3(NEXMIF):c.151C>A (p.Pro51Thr)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Aug 23, 2022