Variant · Snv
ZBTB49 NM_145291.4(ZBTB49):c.1186G>A (p.Ala396Thr)
CI-VAR-00126361Explore in graph →p.Ala396ThrNM_145291.4:c.1186G>AClinVar 777803 rs114306264
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 |
|---|---|---|---|---|---|---|---|---|
| 777803 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma; Uterine corpus endometrial carcinoma; Colorectal cancer; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Clear cell carcinoma of kidney; Gastric cancer; Lung cancer | germline | 3 | Nov 03, 2017 | clinvar |