Variant · Snv
GET4 NM_015949.3(GET4):c.744C>T (p.Asp248=)
CI-VAR-00127528Explore in graph →p.Asp248=NM_015949.3:c.744C>TClinVar 710436 rs41273984
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 |
|---|---|---|---|---|---|---|---|---|
| 710436 | Benign | criteria provided, single submitter | 1 | Gastric cancer; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Lung cancer; Colorectal cancer; Lymphoma; Nonpapillary renal cell carcinoma; Cervical cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Familial cancer of breast; Ovarian cancer; Thymoma; Thyroid cancer, nonmedullary, 1; Melanoma; Cholangiocarcinoma | germline | 2 | Jun 26, 2018 | clinvar |