NM_001110792.2(MECP2):c.1032C>T (p.Ser344=) AND MECP2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004544320.1
Allele description [Variation Report for NM_001110792.2(MECP2):c.1032C>T (p.Ser344=)]
NM_001110792.2(MECP2):c.1032C>T (p.Ser344=)
Condition(s)
- Name:
- MECP2-related disorder
- Synonyms:
- MECP2-Related Disorders; MECP2-related condition
- Identifiers:
- MedGen: C5880921
Assertion and evidence details
Last Updated: Sep 29, 2024