Variant · Snv
TMED3 NM_007364.4(TMED3):c.168+1G>A
CI-VAR-00306113Explore in graph →NM_007364.4:c.168+1G>AClinVar 2645626 rs141194056
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 |
|---|---|---|---|---|---|---|---|---|
| 2645626 | Likely benign | criteria provided, single submitter | 1 | Ovarian serous cystadenocarcinoma; Melanoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Gastric cancer; Colorectal cancer; Sarcoma; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Malignant tumor of urinary bladder; Malignant tumor of esophagus; Lung cancer; Familial cancer of breast | germline | 2 | Apr 01, 2023 | clinvar |