NM_006231.4(POLE):c.802-6C>T AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 6, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003493547.1
Allele description [Variation Report for NM_006231.4(POLE):c.802-6C>T]
NM_006231.4(POLE):c.802-6C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024