NM_001110792.2(MECP2):c.727G>C (p.Gly243Arg) AND Severe neonatal-onset encephalopathy with microcephaly
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003640178.2
Allele description [Variation Report for NM_001110792.2(MECP2):c.727G>C (p.Gly243Arg)]
NM_001110792.2(MECP2):c.727G>C (p.Gly243Arg)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024