Variant · Deletion
RXYLT1 NM_014254.3(RXYLT1):c.170-17_170-14del
CI-VAR-00227260Explore in graph →NM_014254.3:c.170-17_170-14delClinVar 1587287 rs571489273
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 |
|---|---|---|---|---|---|---|---|---|
| 1587287 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10; Familial cancer of breast | germline | 3 | Jan 01, 2026 | clinvar |