NM_001110792.2(MECP2):c.336G>A (p.Leu112=) AND Severe neonatal-onset encephalopathy with microcephaly
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003524698.2
Allele description [Variation Report for NM_001110792.2(MECP2):c.336G>A (p.Leu112=)]
NM_001110792.2(MECP2):c.336G>A (p.Leu112=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024