NM_001379286.1(ZNF423):c.2211C>T (p.Phe737=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003426341.10
Allele description [Variation Report for NM_001379286.1(ZNF423):c.2211C>T (p.Phe737=)]
NM_001379286.1(ZNF423):c.2211C>T (p.Phe737=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024