Variant · Snv
DDR1 NM_001297654.2(DDR1):c.2214C>T (p.Ile738=)
CI-VAR-00127014Explore in graph →p.Ile738=NM_001297654.2:c.2214C>TClinVar 782946 rs147091812
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 |
|---|---|---|---|---|---|---|---|---|
| 782946 | Benign | criteria provided, single submitter | 1 | Sarcoma; Gastric cancer; Lymphoma; Ovarian serous cystadenocarcinoma; Thymoma; Uterine corpus endometrial carcinoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Clear cell carcinoma of kidney; Colorectal cancer; Melanoma; Malignant tumor of esophagus; Familial cancer of breast | germline | 2 | Mar 05, 2018 | clinvar |