NM_001110792.2(MECP2):c.723G>T (p.Ser241=) AND Severe neonatal-onset encephalopathy with microcephaly
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001087926.15
Allele description [Variation Report for NM_001110792.2(MECP2):c.723G>T (p.Ser241=)]
NM_001110792.2(MECP2):c.723G>T (p.Ser241=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024