NM_001110792.2(MECP2):c.246C>T (p.Ser82=) AND History of neurodevelopmental disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 17, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000717918.2
Allele description [Variation Report for NM_001110792.2(MECP2):c.246C>T (p.Ser82=)]
NM_001110792.2(MECP2):c.246C>T (p.Ser82=)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Sep 8, 2024