NM_014687.4(RUBCN):c.2898C>T (p.Ala966=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000974351.9
Allele description [Variation Report for NM_014687.4(RUBCN):c.2898C>T (p.Ala966=)]
NM_014687.4(RUBCN):c.2898C>T (p.Ala966=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024