NM_199420.4(POLQ):c.652T>C (p.Leu218=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004518297.1
Allele description [Variation Report for NM_199420.4(POLQ):c.652T>C (p.Leu218=)]
NM_199420.4(POLQ):c.652T>C (p.Leu218=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024