NM_001110792.2(MECP2):c.737C>A (p.Ala246Asp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 8, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000194296.6
Allele description [Variation Report for NM_001110792.2(MECP2):c.737C>A (p.Ala246Asp)]
NM_001110792.2(MECP2):c.737C>A (p.Ala246Asp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 9, 2023