NM_133433.4(NIPBL):c.2768G>T (p.Gly923Val) AND Cornelia de Lange syndrome 1
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Dec 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000793633.18
Allele description [Variation Report for NM_133433.4(NIPBL):c.2768G>T (p.Gly923Val)]
NM_133433.4(NIPBL):c.2768G>T (p.Gly923Val)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024