Variant · Snv
TRAPPC9 NM_001160372.4(TRAPPC9):c.2799= (p.Gly933=)
CI-VAR-00020504Explore in graph →p.Gly933=NM_001160372.4:c.2799=ClinVar 130630 rs2614718
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 130630 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Inborn genetic diseases; Colon adenocarcinoma; Lymphoma; Hepatocellular carcinoma; Adrenocortical carcinoma, hereditary; Familial pancreatic carcinoma; Gastric cancer; Nonpapillary renal cell carcinoma; Lung cancer; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma; Acute myeloid leukemia; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Ovarian cancer | germline | 7 | Feb 03, 2026 | clinvar |