NM_002691.4(POLD1):c.378C>T (p.Arg126=) AND not specified
- Germline classification:
- Benign/Likely benign (5 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:
- RCV000427145.23
Allele description [Variation Report for NM_002691.4(POLD1):c.378C>T (p.Arg126=)]
NM_002691.4(POLD1):c.378C>T (p.Arg126=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 4, 2024