Variant · Snv
SPEN NM_015001.3(SPEN):c.1635+6C>T
CI-VAR-00303675Explore in graph →NM_015001.3:c.1635+6C>TClinVar 2585664 rs114910457
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 |
|---|---|---|---|---|---|---|---|---|
| 2585664 | Benign | criteria provided, single submitter | 1 | Radio-Tartaglia syndrome; SPEN-related disorder; Uveal melanoma; Sarcoma; Cholangiocarcinoma; Pancreatic adenocarcinoma; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Lung cancer; Cervical cancer | germline | 3 | Apr 11, 2023 | clinvar |