NM_022095.4(ZNF335):c.2167T>G (p.Phe723Val) AND not provided
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Jul 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001511568.20
Allele description [Variation Report for NM_022095.4(ZNF335):c.2167T>G (p.Phe723Val)]
NM_022095.4(ZNF335):c.2167T>G (p.Phe723Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024