Variant · Snv
DCTN1 NM_004082.5(DCTN1):c.3529+5G>A
CI-VAR-00049734Explore in graph →NM_004082.5:c.3529+5G>AClinVar 284990 rs72466494
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 |
|---|---|---|---|---|---|---|---|---|
| 284990 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Neuronopathy, distal hereditary motor, type 7B; Perry syndrome; Amyotrophic lateral sclerosis type 1; Inborn genetic diseases; DCTN1-related disorder; Clear cell carcinoma of kidney; Uveal melanoma; Familial pancreatic carcinoma; Colon adenocarcinoma; Ovarian cancer; Uterine corpus endometrial carcinoma; Sarcoma; Lymphoma; Uterine carcinosarcoma; Adrenocortical carcinoma, hereditary; Cervical cancer; Gastric cancer; Ovarian serous cystadenocarcinoma; Lung cancer; Familial cancer of breast; Cholangiocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma | germline | 15 | Jun 01, 2026 | clinvar |