Variant · Snv
ACTG1 NM_001614.5(ACTG1):c.-7+135C>T
CI-VAR-00094069Explore in graph →NM_001614.5:c.-7+135C>TClinVar 516171 rs28698582
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 |
|---|---|---|---|---|---|---|---|---|
| 516171 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Sarcoma; Uterine carcinosarcoma; Thymoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Malignant tumor of esophagus; Cervical cancer; Lung cancer; Familial cancer of breast | germline | 3 | Jun 05, 2017 | clinvar |