NM_014795.4(ZEB2):c.2361T>C (p.Asn787=) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Dec 3, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000126370.15
Allele description [Variation Report for NM_014795.4(ZEB2):c.2361T>C (p.Asn787=)]
NM_014795.4(ZEB2):c.2361T>C (p.Asn787=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024