Variant · Snv
ARID4A NM_002892.4(ARID4A):c.3211+1G>A
CI-VAR-00049623Explore in graph →NM_002892.4:c.3211+1G>AClinVar 281165 rs62621193
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 |
|---|---|---|---|---|---|---|---|---|
| 281165 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Colorectal cancer; Gastric cancer; Acute myeloid leukemia; Malignant tumor of esophagus; Colon adenocarcinoma; Sarcoma; Melanoma; Hepatocellular carcinoma; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Uveal melanoma; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer; Familial cancer of breast; Lymphoma; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma; Thyroid cancer, nonmedullary, 1 | germline | 3 | May 28, 2019 | clinvar |