NM_001081.4(CUBN):c.1659C>T (p.Leu553=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 23, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000976059.3
Allele description [Variation Report for NM_001081.4(CUBN):c.1659C>T (p.Leu553=)]
NM_001081.4(CUBN):c.1659C>T (p.Leu553=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022