Variant · Snv
CNKSR1 NM_006314.3(CNKSR1):c.1041G>A (p.Pro347=)
CI-VAR-00126265Explore in graph →p.Pro347=NM_006314.3:c.1041G>AClinVar 778230 rs148237566
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 |
|---|---|---|---|---|---|---|---|---|
| 778230 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Familial cancer of breast; Colorectal cancer; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Clear cell carcinoma of kidney; Acute myeloid leukemia; Cervical cancer; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus | germline | 4 | Dec 01, 2022 | clinvar |