Variant · Snv
DOCK7 NM_001367561.1(DOCK7):c.1872-8G>T
CI-VAR-00072399Explore in graph →NM_001367561.1:c.1872-8G>TClinVar 475131 rs79716948
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 |
|---|---|---|---|---|---|---|---|---|
| 475131 | Likely benign | criteria provided, single submitter | 1 | Developmental and epileptic encephalopathy, 23; Gastric cancer; Lung cancer; Uterine corpus endometrial carcinoma; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus | germline | 2 | Jan 15, 2026 | clinvar |