NM_001367624.2(ZNF469):c.8705C>T (p.Thr2902Met) AND not provided
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Jan 30, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000584880.24
Allele description [Variation Report for NM_001367624.2(ZNF469):c.8705C>T (p.Thr2902Met)]
NM_001367624.2(ZNF469):c.8705C>T (p.Thr2902Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024