NM_001079872.2(CUL4B):c.360CTC[5] (p.Ser128del) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 27, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000477980.1
Allele description
NM_001079872.2(CUL4B):c.360CTC[5] (p.Ser128del)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 24, 2021