Variant · Snv
TOR1AIP1 NM_015602.4(TOR1AIP1):c.964+1G>A
CI-VAR-00072121Explore in graph →NM_015602.4:c.964+1G>AClinVar 476292 rs2274955
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 |
|---|---|---|---|---|---|---|---|---|
| 476292 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Autosomal recessive limb-girdle muscular dystrophy type 2Y; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Malignant tumor of urinary bladder; Hepatocellular carcinoma; Gastric cancer; Papillary renal cell carcinoma type 1; Malignant tumor of esophagus; Colon adenocarcinoma; Uterine carcinosarcoma; Cervical cancer; Adrenocortical carcinoma, hereditary; Familial cancer of breast; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Ovarian cancer | germline | 6 | Feb 01, 2026 | clinvar |