Variant · Snv
ANLN NM_018685.5(ANLN):c.2971-12T>G
CI-VAR-00196164Explore in graph →NM_018685.5:c.2971-12T>GClinVar 1168523 rs6954957
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1168523 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Focal segmental glomerulosclerosis 8; Ovarian serous cystadenocarcinoma; Thymoma; Acute myeloid leukemia; Malignant tumor of esophagus; Malignant lymphoma, large B-cell, diffuse; Gastric cancer; Lung cancer; Ovarian cancer; Uterine corpus endometrial carcinoma; Uveal melanoma; Sarcoma; Cervical cancer | germline | 5 | Apr 01, 2026 | clinvar |