NM_006231.3(POLE):c.207C>T (p.Thr69=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 28, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000439361.2
Allele description
NM_006231.3(POLE):c.207C>T (p.Thr69=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 23, 2021