NM_005993.5(TBCD):c.625G>A (p.Val209Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 3, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000624872.2
Allele description [Variation Report for NM_005993.5(TBCD):c.625G>A (p.Val209Ile)]
NM_005993.5(TBCD):c.625G>A (p.Val209Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Feb 7, 2023