Variant · Snv
DYNC2LI1 NM_016008.4(DYNC2LI1):c.732-5C>T
CI-VAR-00200334Explore in graph →NM_016008.4:c.732-5C>TClinVar 1267824 rs17495522
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 |
|---|---|---|---|---|---|---|---|---|
| 1267824 | Benign | criteria provided, multiple submitters, no conflicts | 2 | DYNC2LI1-related disorder; Uterine carcinosarcoma; Thymoma; Acute myeloid leukemia; Malignant tumor of esophagus; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Uveal melanoma; Colorectal cancer; Gastric cancer; Nonpapillary renal cell carcinoma; Lung cancer; Colon adenocarcinoma; Sarcoma; Adrenocortical carcinoma, hereditary; Cervical cancer | germline | 4 | Jan 27, 2026 | clinvar |