Variant · Snv
SLC35D1 NM_015139.3(SLC35D1):c.729+5G>C
CI-VAR-00196031Explore in graph →NM_015139.3:c.729+5G>CClinVar 1168661 rs7539628
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 |
|---|---|---|---|---|---|---|---|---|
| 1168661 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Schneckenbecken dysplasia; Clear cell carcinoma of kidney; Cholangiocarcinoma; Malignant tumor of esophagus; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Thymoma; Acute myeloid leukemia; Colorectal cancer; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer | germline | 4 | Feb 01, 2026 | clinvar |