Variant · Snv
KPNA4 NM_002268.5(KPNA4):c.115-3A>T
CI-VAR-00306282Explore in graph →NM_002268.5:c.115-3A>TClinVar 2654259 rs1421471586
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 2654259 | Likely benign | criteria provided, single submitter | 1 | Gastric cancer; Cholangiocarcinoma; Acute myeloid leukemia; Malignant tumor of urinary bladder; Lung cancer | germline | 2 | Jul 01, 2023 | clinvar |