Variant · Snv
TTC12 NM_017868.4(TTC12):c.1446+2T>C
CI-VAR-00338610Explore in graph →NM_017868.4:c.1446+2T>CClinVar 3034669 rs77534773
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 |
|---|---|---|---|---|---|---|---|---|
| 3034669 | Benign | criteria provided, single submitter | 1 | TTC12-related disorder; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus; Cervical cancer; Familial cancer of breast; Sarcoma; Papillary renal cell carcinoma type 1; Hepatocellular carcinoma | germline | 3 | Apr 01, 2026 | clinvar |