Variant · Snv
SPTAN1 NM_001130438.3(SPTAN1):c.6708-7C>T
CI-VAR-00022556Explore in graph →NM_001130438.3:c.6708-7C>TClinVar 139312 rs16930539
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 |
|---|---|---|---|---|---|---|---|---|
| 139312 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Developmental and epileptic encephalopathy, 5; Clear cell carcinoma of kidney; Thyroid cancer, nonmedullary, 1; Nonpapillary renal cell carcinoma; Uterine corpus endometrial carcinoma; Malignant tumor of esophagus; Lung cancer; Cervical cancer; Early-infantile DEE; Sarcoma; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma | germline | 8 | Feb 03, 2026 | clinvar |