NM_006502.3(POLH):c.2028C>T (p.Ala676=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001550335.23
Allele description [Variation Report for NM_006502.3(POLH):c.2028C>T (p.Ala676=)]
NM_006502.3(POLH):c.2028C>T (p.Ala676=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024