NM_001110792.2(MECP2):c.563C>T (p.Pro188Leu) AND Rett syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 6, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002244934.2
Allele description [Variation Report for NM_001110792.2(MECP2):c.563C>T (p.Pro188Leu)]
NM_001110792.2(MECP2):c.563C>T (p.Pro188Leu)
Condition(s)
Assertion and evidence details
Last Updated: Feb 7, 2023