Variant · Snv
GLUL NM_001033044.4(GLUL):c.603+5G>A
CI-VAR-00050133Explore in graph →NM_001033044.4:c.603+5G>AClinVar 293945 rs140378060
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 |
|---|---|---|---|---|---|---|---|---|
| 293945 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Congenital brain dysgenesis due to glutamine synthetase deficiency; GLUL-related disorder; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uveal melanoma; Clear cell carcinoma of kidney; Nonpapillary renal cell carcinoma; Lung cancer; Colon adenocarcinoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Familial cancer of breast; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Thymoma | germline | 6 | Feb 01, 2026 | clinvar |