NM_016203.4(PRKAG2):c.1372T>G (p.Ser458Ala) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 4, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000521039.2
Allele description [Variation Report for NM_016203.4(PRKAG2):c.1372T>G (p.Ser458Ala)]
NM_016203.4(PRKAG2):c.1372T>G (p.Ser458Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jul 29, 2023