Variant · Snv
DYNC2I1 NM_018051.5(DYNC2I1):c.490G>A (p.Val164Ile)
CI-VAR-00093484Explore in graph →p.Val164IleNM_018051.5:c.490G>AClinVar 516235 rs78313003
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 |
|---|---|---|---|---|---|---|---|---|
| 516235 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Short-rib thoracic dysplasia 8 with or without polydactyly; Colorectal cancer; Gastric cancer; Nonpapillary renal cell carcinoma; Cervical cancer; Colon adenocarcinoma; Sarcoma; Lymphoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Thymoma; Cholangiocarcinoma; Acute myeloid leukemia; Hepatocellular carcinoma; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Ovarian cancer | germline | 5 | Feb 04, 2026 | clinvar |