NM_001110792.2(MECP2):c.1197C>T (p.Pro399=) AND Rett syndrome
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Mar 14, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000172863.3
Allele description [Variation Report for NM_001110792.2(MECP2):c.1197C>T (p.Pro399=)]
NM_001110792.2(MECP2):c.1197C>T (p.Pro399=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024