Variant · Snv
DYNC2I1 NM_018051.5(DYNC2I1):c.990+3A>T
CI-VAR-00168897Explore in graph →NM_018051.5:c.990+3A>TClinVar 968954 rs374608321
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 968954 | Uncertain significance | criteria provided, single submitter | 1 | Short-rib thoracic dysplasia 8 with or without polydactyly; Clear cell carcinoma of kidney; Lung cancer | germline | 2 | Oct 22, 2024 | clinvar |