NM_002693.3(POLG):c.3294T>C (p.Asn1098=) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- May 19, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000127536.9
Allele description [Variation Report for NM_002693.3(POLG):c.3294T>C (p.Asn1098=)]
NM_002693.3(POLG):c.3294T>C (p.Asn1098=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024