NM_030665.4(RAI1):c.851_852insACAGCAGCAGCA (p.Gln288_Gln291dup) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 1, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002314600.9
Allele description [Variation Report for NM_030665.4(RAI1):c.851_852insACAGCAGCAGCA (p.Gln288_Gln291dup)]
NM_030665.4(RAI1):c.851_852insACAGCAGCAGCA (p.Gln288_Gln291dup)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 8, 2024