Variant · Snv
SELENON NM_206926.2(SELENON):c.307A>G (p.Thr103Ala)
CI-VAR-00020484Explore in graph →p.Thr103AlaNM_206926.2:c.307A>GClinVar 130284 rs35019869
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 130284 | Benign | criteria provided, multiple submitters, no conflicts | 2 | SEPN1-related disorder; Eichsfeld type congenital muscular dystrophy; Cervical cancer; Clear cell carcinoma of kidney; Colon adenocarcinoma; Uterine corpus endometrial carcinoma; Thymoma; Colorectal cancer; Sarcoma; Melanoma; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia | germline | 12 | Feb 04, 2026 | clinvar |