NM_133433.4(NIPBL):c.198C>G (p.Val66=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 13, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002415583.2
Allele description [Variation Report for NM_133433.4(NIPBL):c.198C>G (p.Val66=)]
NM_133433.4(NIPBL):c.198C>G (p.Val66=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024