NM_002693.3(POLG):c.3442C>T (p.Arg1148Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 19, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002456072.2
Allele description [Variation Report for NM_002693.3(POLG):c.3442C>T (p.Arg1148Cys)]
NM_002693.3(POLG):c.3442C>T (p.Arg1148Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 12, 2024