NM_001110792.2(MECP2):c.462C>T (p.Phe154=) AND Severe neonatal-onset encephalopathy with microcephaly
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000645137.11
Allele description [Variation Report for NM_001110792.2(MECP2):c.462C>T (p.Phe154=)]
NM_001110792.2(MECP2):c.462C>T (p.Phe154=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024