Variant · Snv
TCF3 NM_003200.5(TCF3):c.302A>G (p.Lys101Arg)
CI-VAR-00134882Explore in graph →p.Lys101ArgNM_003200.5:c.302A>GClinVar 810990 rs41275842
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 |
|---|---|---|---|---|---|---|---|---|
| 810990 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | TCF3-related disorder; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Cervical cancer; Thyroid cancer, nonmedullary, 1; Melanoma; Cholangiocarcinoma; Acute myeloid leukemia; Hepatocellular carcinoma; Uterine corpus endometrial carcinoma; Uveal melanoma; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Gastric cancer; Uterine carcinosarcoma; Thymoma; Nonpapillary renal cell carcinoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Lung cancer | germline | 7 | Jun 01, 2026 | clinvar |