NM_000162.5(GCK):c.477C>G (p.Ile159Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 30, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000518112.3
Allele description [Variation Report for NM_000162.5(GCK):c.477C>G (p.Ile159Met)]
NM_000162.5(GCK):c.477C>G (p.Ile159Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024