NM_003384.3(VRK1):c.976C>T (p.Gln326Ter) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Feb 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001592942.12
Allele description [Variation Report for NM_003384.3(VRK1):c.976C>T (p.Gln326Ter)]
NM_003384.3(VRK1):c.976C>T (p.Gln326Ter)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Nov 24, 2024