NM_001379286.1(ZNF423):c.1176G>A (p.Pro392=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 17, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000592535.4
Allele description [Variation Report for NM_001379286.1(ZNF423):c.1176G>A (p.Pro392=)]
NM_001379286.1(ZNF423):c.1176G>A (p.Pro392=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024