NM_174916.3(UBR1):c.888T>C (p.His296=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003849896.1
Allele description [Variation Report for NM_174916.3(UBR1):c.888T>C (p.His296=)]
NM_174916.3(UBR1):c.888T>C (p.His296=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024