NM_000553.6(WRN):c.3120T>C (p.Ile1040=) AND Werner syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003614650.1
Allele description [Variation Report for NM_000553.6(WRN):c.3120T>C (p.Ile1040=)]
NM_000553.6(WRN):c.3120T>C (p.Ile1040=)
Condition(s)
-
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Last Updated: Feb 28, 2024