NM_001110792.2(MECP2):c.333C>G (p.Thr111=) AND Rett syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003380474.1
Allele description [Variation Report for NM_001110792.2(MECP2):c.333C>G (p.Thr111=)]
NM_001110792.2(MECP2):c.333C>G (p.Thr111=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 28, 2023