NM_001378120.1(MBD5):c.2162C>T (p.Pro721Leu) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002314732.8
Allele description [Variation Report for NM_001378120.1(MBD5):c.2162C>T (p.Pro721Leu)]
NM_001378120.1(MBD5):c.2162C>T (p.Pro721Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Jun 29, 2024