Variant · Snv
DONSON NM_017613.4(DONSON):c.1388G>T (p.Gly463Val)
CI-VAR-00235004Explore in graph →p.Gly463ValNM_017613.4:c.1388G>TClinVar 1565389 rs190773441
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 |
|---|---|---|---|---|---|---|---|---|
| 1565389 | Benign | criteria provided, multiple submitters, no conflicts | 2 | DONSON-related disorder; Malignant lymphoma, large B-cell, diffuse; Thymoma; Hepatocellular carcinoma; Uterine corpus endometrial carcinoma | germline | 4 | Nov 24, 2025 | clinvar |