NM_000553.6(WRN):c.3122G>C (p.Cys1041Ser) AND Werner syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003504618.1
Allele description [Variation Report for NM_000553.6(WRN):c.3122G>C (p.Cys1041Ser)]
NM_000553.6(WRN):c.3122G>C (p.Cys1041Ser)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024