NM_001160372.4(TRAPPC9):c.1693G>A (p.Val565Met) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004020346.1
Allele description [Variation Report for NM_001160372.4(TRAPPC9):c.1693G>A (p.Val565Met)]
NM_001160372.4(TRAPPC9):c.1693G>A (p.Val565Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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UI-R-CT0s-cau-h-03-0-UI.s1 UI-R-CT0s Rattus norvegicus cDNA clone UI-R-CT0s-cau-...
UI-R-CT0s-cau-h-03-0-UI.s1 UI-R-CT0s Rattus norvegicus cDNA clone UI-R-CT0s-cau-h-03-0-UI 3', mRNA sequencegi|14931592|gnl|dbEST|9084605|gb|BI 9.1|Nucleotide
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Last Updated: May 26, 2024