Variant · Snv
TPP1 NM_000391.4(TPP1):c.1266+5G>A
CI-VAR-00020501Explore in graph →NM_000391.4:c.1266+5G>AClinVar 130606 rs1800753
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 |
|---|---|---|---|---|---|---|---|---|
| 130606 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Neuronal ceroid lipofuscinosis 2; Inborn genetic diseases; Autosomal recessive spinocerebellar ataxia 7; Gastric cancer; Thymoma; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Lung cancer; Cervical cancer; Familial cancer of breast; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Sarcoma | germline | 17 | Feb 04, 2026 | clinvar |