NM_001137608.3(ZNF732):c.722A>T (p.His241Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004244474.1
Allele description [Variation Report for NM_001137608.3(ZNF732):c.722A>T (p.His241Leu)]
NM_001137608.3(ZNF732):c.722A>T (p.His241Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024