Variant · Snv
ANKRD26 NM_014915.3(ANKRD26):c.2697+58A>G
CI-VAR-00200730Explore in graph →NM_014915.3:c.2697+58A>GClinVar 1279852 rs41279940
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 |
|---|---|---|---|---|---|---|---|---|
| 1279852 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Thrombocytopenia 2; Thymoma; Malignant tumor of esophagus; Uveal melanoma; Malignant lymphoma, large B-cell, diffuse; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia | germline | 4 | Dec 05, 2021 | clinvar |