NM_001378120.1(MBD5):c.5014C>T (p.Arg1672Cys) AND Intellectual disability, autosomal dominant 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001034501.8
Allele description [Variation Report for NM_001378120.1(MBD5):c.5014C>T (p.Arg1672Cys)]
NM_001378120.1(MBD5):c.5014C>T (p.Arg1672Cys)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024