NM_178544.5(ZNF546):c.791A>T (p.His264Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004305776.1
Allele description [Variation Report for NM_178544.5(ZNF546):c.791A>T (p.His264Leu)]
NM_178544.5(ZNF546):c.791A>T (p.His264Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024