NM_001110792.2(MECP2):c.1150C>T (p.His384Tyr) AND Severe neonatal-onset encephalopathy with microcephaly
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001242465.7
Allele description [Variation Report for NM_001110792.2(MECP2):c.1150C>T (p.His384Tyr)]
NM_001110792.2(MECP2):c.1150C>T (p.His384Tyr)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024