NM_024426.6(WT1):c.162C>G (p.Ser54Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003165825.1
Allele description [Variation Report for NM_024426.6(WT1):c.162C>G (p.Ser54Arg)]
NM_024426.6(WT1):c.162C>G (p.Ser54Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Jun 9, 2024