NM_001378120.1(MBD5):c.27A>T (p.Gly9=) AND Intellectual disability, autosomal dominant 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003601607.1
Allele description [Variation Report for NM_001378120.1(MBD5):c.27A>T (p.Gly9=)]
NM_001378120.1(MBD5):c.27A>T (p.Gly9=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024