Variant · Snv
ITPA NM_033453.4(ITPA):c.264-12T>G
CI-VAR-00196426Explore in graph →NM_033453.4:c.264-12T>GClinVar 1167141 rs8114386
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 |
|---|---|---|---|---|---|---|---|---|
| 1167141 | Benign | criteria provided, single submitter | 1 | Inosine triphosphatase deficiency; Uterine corpus endometrial carcinoma; Acute myeloid leukemia; Cervical cancer; Familial cancer of breast | germline | 2 | Feb 04, 2026 | clinvar |