Variant · Snv
AIMP1 NM_001142416.2(AIMP1):c.-25-6C>A
CI-VAR-00200767Explore in graph →NM_001142416.2:c.-25-6C>AClinVar 1279491 rs3737498
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1279491 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Ovarian cancer; Uterine carcinosarcoma; Germ cell tumor of testis; Malignant lymphoma, large B-cell, diffuse; Nonpapillary renal cell carcinoma; Familial cancer of breast; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uveal melanoma | germline | 5 | Nov 26, 2024 | clinvar |