NM_001199107.2(TBC1D24):c.759G>A (p.Lys253=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 26, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002390662.2
Allele description [Variation Report for NM_001199107.2(TBC1D24):c.759G>A (p.Lys253=)]
NM_001199107.2(TBC1D24):c.759G>A (p.Lys253=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024