NM_001110792.2(MECP2):c.1174G>A (p.Val392Met) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 22, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002321616.9
Allele description [Variation Report for NM_001110792.2(MECP2):c.1174G>A (p.Val392Met)]
NM_001110792.2(MECP2):c.1174G>A (p.Val392Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 8, 2024