Variant · Snv
TTLL1 NM_012263.5(TTLL1):c.894G>A (p.Pro298=)
CI-VAR-00058693Explore in graph →p.Pro298=NM_012263.5:c.894G>AClinVar 403577 rs9607998
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 |
|---|---|---|---|---|---|---|---|---|
| 403577 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Colorectal cancer; Sarcoma; Gastric cancer; Uterine carcinosarcoma; Uveal melanoma; Thymoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Uterine corpus endometrial carcinoma; Cholangiocarcinoma; Malignant tumor of esophagus | germline | 3 | Mar 29, 2016 | clinvar |