Variant · Deletion
CARS2 NM_024537.4(CARS2):c.572-3_572-2del
CI-VAR-00067492Explore in graph →NM_024537.4:c.572-3_572-2delClinVar 421531 rs201758363
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 |
|---|---|---|---|---|---|---|---|---|
| 421531 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Combined oxidative phosphorylation defect type 27; Clear cell carcinoma of kidney; Papillary renal cell carcinoma type 1; Familial cancer of breast; Colon adenocarcinoma | germline | 5 | Apr 01, 2026 | clinvar |