Variant · Snv
PTCH1 Q787X
CI-VAR-00003592Explore in graph →CIViC 1592
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.
- 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
- 19726763
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Basal Cell Carcinoma1 | ||||||||
| PTCH1 Q787X | Vismodegib | Predictive | C | Supports Sensitivity Response | — | submitted | EID4683In a phase 1 study (NCT00607724), an advanced, chemotherapy-refractory basal cell carcinoma patient harboring a PTCH1 Q938* nonsense mutation was associated with a partial response to vismodegib monot… (full text at CIViC) PMID 19726763 · Von Hoff et al., 2009 · 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