Variant · Snv
GLB1 NM_000404.4(GLB1):c.458-11T>C
CI-VAR-00018037Explore in graph →NM_000404.4:c.458-11T>CClinVar 92909 rs34204221
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 92909 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Mucopolysaccharidosis, MPS-IV-B; GM1 gangliosidosis; Infantile GM1 gangliosidosis; Thymoma; Nonpapillary renal cell carcinoma; Familial cancer of breast; Ovarian cancer; Familial pancreatic carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Gastric cancer | germline | 12 | Feb 04, 2026 | clinvar |