NM_006231.4(POLE):c.16G>C (p.Gly6Arg) AND not specified
- Germline classification:
- Benign/Likely benign (6 submissions)
- Last evaluated:
- Aug 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000202795.17
Allele description [Variation Report for NM_006231.4(POLE):c.16G>C (p.Gly6Arg)]
NM_006231.4(POLE):c.16G>C (p.Gly6Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024