NM_006231.4(POLE):c.3459+13T>G AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 5, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000418047.1
Allele description [Variation Report for NM_006231.4(POLE):c.3459+13T>G]
NM_006231.4(POLE):c.3459+13T>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024