Variant · Snv
ATIC NM_004044.7(ATIC):c.1443A>G (p.Gly481=)
CI-VAR-00236073Explore in graph →p.Gly481=NM_004044.7:c.1443A>GClinVar 1600148 rs112288749
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 |
|---|---|---|---|---|---|---|---|---|
| 1600148 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Thymoma; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Uveal melanoma; Germ cell tumor of testis; Lung cancer; Cervical cancer; Colon adenocarcinoma; Sarcoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Colorectal cancer; Gastric cancer; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma | germline | 3 | Dec 19, 2025 | clinvar |