Variant · Snv
SPG11 NM_025137.4(SPG11):c.5121G>T (p.Glu1707Asp)
CI-VAR-00063420Explore in graph →p.Glu1707AspNM_025137.4:c.5121G>TClinVar 406519 rs145643238
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 |
|---|---|---|---|---|---|---|---|---|
| 406519 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Hereditary spastic paraplegia 11; Intellectual disability; Inborn genetic diseases; Amyotrophic lateral sclerosis type 5; Charcot-Marie-Tooth disease axonal type 2X; SPG11-related disorder; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus | germline | 19 | Feb 01, 2026 | clinvar |