Variant · Other
PRKRA NM_003690.5(PRKRA):c.610-11_610-10del
CI-VAR-00050358Explore in graph →NM_003690.5:c.610-11_610-10delClinVar 332625 rs138320145
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 |
|---|---|---|---|---|---|---|---|---|
| 332625 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Dystonia 16; Colon adenocarcinoma; Colorectal cancer; Lymphoma; Cholangiocarcinoma; Uveal melanoma; Malignant lymphoma, large B-cell, diffuse; Malignant tumor of esophagus; Familial cancer of breast; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Nonpapillary renal cell carcinoma; Ovarian cancer | germline | 4 | Feb 04, 2026 | clinvar |