Variant · Snv
FUS NM_004960.4(FUS):c.153C>T (p.Gly51=)
CI-VAR-00047557Explore in graph →p.Gly51=NM_004960.4:c.153C>TClinVar 259595 rs61733962
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 |
|---|---|---|---|---|---|---|---|---|
| 259595 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Amyotrophic lateral sclerosis type 6; Tremor, hereditary essential, 4; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Uterine corpus endometrial carcinoma; Uveal melanoma; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Adrenocortical carcinoma, hereditary; Cervical cancer; Colon adenocarcinoma; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Clear cell carcinoma of kidney; Thymoma; Melanoma; Lung cancer | germline | 9 | Feb 02, 2026 | clinvar |