Variant · Snv
TASP1 NM_017714.3(TASP1):c.327G>T (p.Leu109=)
CI-VAR-00338715Explore in graph →p.Leu109=NM_017714.3:c.327G>TClinVar 3034428 rs117248024
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 3034428 | Benign | no assertion criteria provided | 0 | TASP1-related disorder; Sarcoma; Ovarian serous cystadenocarcinoma; Malignant tumor of urinary bladder; Malignant tumor of esophagus; Clear cell carcinoma of kidney; Cervical cancer; Familial cancer of breast; Thymoma; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Colorectal cancer; Gastric cancer; Hepatocellular carcinoma; Lung cancer | germline | 2 | Nov 12, 2019 | clinvar |