NM_181552.4(CUX1):c.2995T>A (p.Phe999Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003443476.1
Allele description [Variation Report for NM_181552.4(CUX1):c.2995T>A (p.Phe999Ile)]
NM_181552.4(CUX1):c.2995T>A (p.Phe999Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Nov 25, 2023