NM_000162.5(GCK):c.1190G>A (p.Arg397His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 10, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001288975.3
Allele description [Variation Report for NM_000162.5(GCK):c.1190G>A (p.Arg397His)]
NM_000162.5(GCK):c.1190G>A (p.Arg397His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024