Variant · Snv
ALG3 NM_005787.6(ALG3):c.319A>G (p.Ile107Val)
CI-VAR-00050893Explore in graph →p.Ile107ValNM_005787.6:c.319A>GClinVar 344358 rs2233463
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 |
|---|---|---|---|---|---|---|---|---|
| 344358 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | ALG3-congenital disorder of glycosylation; Thyroid cancer, nonmedullary, 1; Melanoma; Cholangiocarcinoma; Acute myeloid leukemia; Colon adenocarcinoma; Sarcoma; Malignant tumor of esophagus; Lung cancer; Clear cell carcinoma of kidney; Uveal melanoma; Cervical cancer; Colorectal cancer; Thymoma; Hepatocellular carcinoma; Adrenocortical carcinoma, hereditary | germline | 7 | Jun 01, 2026 | clinvar |