NM_001278716.2(FBXL4):c.1555C>T (p.Gln519Ter) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Dec 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001090674.21
Allele description [Variation Report for NM_001278716.2(FBXL4):c.1555C>T (p.Gln519Ter)]
NM_001278716.2(FBXL4):c.1555C>T (p.Gln519Ter)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024