NM_001382430.1(AKT1):c.1113G>C (p.Thr371=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002439016.1
Allele description [Variation Report for NM_001382430.1(AKT1):c.1113G>C (p.Thr371=)]
NM_001382430.1(AKT1):c.1113G>C (p.Thr371=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Feb 28, 2024