NM_016203.4(PRKAG2):c.1015T>A (p.Tyr339Asn) AND Lethal congenital glycogen storage disease of heart
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001958049.6
Allele description [Variation Report for NM_016203.4(PRKAG2):c.1015T>A (p.Tyr339Asn)]
NM_016203.4(PRKAG2):c.1015T>A (p.Tyr339Asn)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024