NM_001110792.2(MECP2):c.1120C>G (p.Pro374Ala) AND Severe neonatal-onset encephalopathy with microcephaly
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000547379.9
Allele description [Variation Report for NM_001110792.2(MECP2):c.1120C>G (p.Pro374Ala)]
NM_001110792.2(MECP2):c.1120C>G (p.Pro374Ala)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024