NM_000553.6(WRN):c.59A>G (p.Asn20Ser) AND Werner syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002043071.4
Allele description [Variation Report for NM_000553.6(WRN):c.59A>G (p.Asn20Ser)]
NM_000553.6(WRN):c.59A>G (p.Asn20Ser)
Condition(s)
-
FAM110A family with sequence similarity 110 member A [Homo sapiens]
FAM110A family with sequence similarity 110 member A [Homo sapiens]Gene ID:83541Gene
-
Gene Links for GEO Profiles (Select 128625378) (1)
Gene
-
Taxonomy Links for Protein (Select 756761759) (1)
Taxonomy
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Last Updated: Dec 24, 2023