NM_207395.3(ZNF324B):c.1282G>C (p.Ala428Pro) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002788493.1
Allele description [Variation Report for NM_207395.3(ZNF324B):c.1282G>C (p.Ala428Pro)]
NM_207395.3(ZNF324B):c.1282G>C (p.Ala428Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Feb 13, 2023