NM_000162.5(GCK):c.397T>C (p.Phe133Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001844289.1
Allele description [Variation Report for NM_000162.5(GCK):c.397T>C (p.Phe133Leu)]
NM_000162.5(GCK):c.397T>C (p.Phe133Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024