NM_014780.5(CUL7):c.1215C>T (p.Asn405=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000974211.7
Allele description [Variation Report for NM_014780.5(CUL7):c.1215C>T (p.Asn405=)]
NM_014780.5(CUL7):c.1215C>T (p.Asn405=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024