NM_004380.3(CREBBP):c.879G>A (p.Val293=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 12, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002377024.3
Allele description [Variation Report for NM_004380.3(CREBBP):c.879G>A (p.Val293=)]
NM_004380.3(CREBBP):c.879G>A (p.Val293=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
histone H2B type 2-E [Homo sapiens]
histone H2B type 2-E [Homo sapiens]gi|4504277|ref|NP_003519.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 8, 2024