Variant · Snv
TPCN1 NM_017901.6(TPCN1):c.2114-3C>T
CI-VAR-00132404Explore in graph →NM_017901.6:c.2114-3C>TClinVar 779354 rs11837633
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 |
|---|---|---|---|---|---|---|---|---|
| 779354 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Uterine carcinosarcoma; Melanoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Malignant tumor of esophagus; Colorectal cancer; Ovarian serous cystadenocarcinoma; Adrenocortical carcinoma, hereditary; Cervical cancer; Colon adenocarcinoma; Gastric cancer; Lung cancer | germline | 3 | Jul 13, 2018 | clinvar |