Variant · Snv
SLC37A3 NM_207113.3(SLC37A3):c.1174+5G>A
CI-VAR-00395048Explore in graph →NM_207113.3:c.1174+5G>AClinVar 4280740
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 |
|---|---|---|---|---|---|---|---|---|
| 4280740 | Benign | criteria provided, single submitter | 1 | Gastric cancer; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Ovarian cancer; Familial pancreatic carcinoma; Colorectal cancer; Nonpapillary renal cell carcinoma; Cervical cancer; Clear cell carcinoma of kidney; Colon adenocarcinoma; Sarcoma; Malignant tumor of esophagus; Lung cancer | germline | 2 | Oct 01, 2025 | clinvar |