Variant · Snv
DOCK6 NM_020812.4(DOCK6):c.4203G>A (p.Gln1401=)
CI-VAR-00196407Explore in graph →p.Gln1401=NM_020812.4:c.4203G>AClinVar 1166359 rs8110957
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 |
|---|---|---|---|---|---|---|---|---|
| 1166359 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Clear cell carcinoma of kidney; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Thymoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Colorectal cancer; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Lung cancer; Cervical cancer | germline | 4 | Feb 02, 2026 | clinvar |