NM_004380.3(CREBBP):c.7212A>G (p.Glu2404=) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 17, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002311618.9
Allele description [Variation Report for NM_004380.3(CREBBP):c.7212A>G (p.Glu2404=)]
NM_004380.3(CREBBP):c.7212A>G (p.Glu2404=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 19, 2024