Variant · Snv
RAB3GAP2 NM_012414.4(RAB3GAP2):c.2587A>G (p.Thr863Ala)
CI-VAR-00020463Explore in graph →p.Thr863AlaNM_012414.4:c.2587A>GClinVar 130078 rs12045447
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 |
|---|---|---|---|---|---|---|---|---|
| 130078 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Warburg micro syndrome 2; Martsolf syndrome; Acute myeloid leukemia; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Lymphoma; Thymoma; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Colorectal cancer; Uterine carcinosarcoma; Cholangiocarcinoma | germline | 10 | Feb 03, 2026 | clinvar |