Variant · Snv
ST7 NM_001369598.1(ST7):c.1638+860G>T
CI-VAR-00126428Explore in graph →NM_001369598.1:c.1638+860G>TClinVar 774316 rs35196356
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 |
|---|---|---|---|---|---|---|---|---|
| 774316 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Lung cancer; Uterine corpus endometrial carcinoma; Gastric cancer; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary | germline | 3 | Dec 31, 2019 | clinvar |