NM_000553.6(WRN):c.26C>T (p.Thr9Ile) AND Werner syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001057691.4
Allele description [Variation Report for NM_000553.6(WRN):c.26C>T (p.Thr9Ile)]
NM_000553.6(WRN):c.26C>T (p.Thr9Ile)
Condition(s)
-
Scyl1 SCY1 like pseudokinase 1 [Rattus norvegicus]
Scyl1 SCY1 like pseudokinase 1 [Rattus norvegicus]Gene ID:293684Gene
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Last Updated: Feb 20, 2024