Variant · Indel
VHL F148Lfs*11 (c.444del)
CI-VAR-00001086Explore in graph →CIViC 3129
Curated evidence
Evidence by cancer (1 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.
civicProvenance
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 8641695
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Von Hippel-Lindau Disease1unmapped disease | ||||||||
| VHL F148Lfs*11 (c.444del) | (predisposing) | Predisposing | C | N/A N/A | 3 | submitted | EID8565A case report describes a a 29-year-old man presenting with recurrent spinal hemangioblastomas and a negative family history for VHL. PCR/SSCP analysis with primers from the VHL gene identified a dele… (full text at CIViC) PMID 8641695 · Decker et al., 1996 · Open in CIViC | civic |
ClinVar
Clinical significance (0)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
Data not yet available
No ClinVar interpretation attached to this variant.