NM_016203.4(PRKAG2):c.477CTC[2] (p.Ser162del) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002265863.1
Allele description [Variation Report for NM_016203.4(PRKAG2):c.477CTC[2] (p.Ser162del)]
NM_016203.4(PRKAG2):c.477CTC[2] (p.Ser162del)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024