Variant · Snv
PDGFRA D842V
CI-VAR-00000587Explore in graph →NP_006197.1:p.Asp842ValNM_006206.4:c.2525A>TClinVar 13543 CIViC 99 rs121908585
Curated evidence
Evidence by cancer (18 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
- 19039322
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Chronic Myeloid Leukemia, BCR-ABL1 Positive1 | ||||||||
| PDGFRA D842V | Bosutinib | Predictive | D | Supports Sensitivity Response | 2 | submitted | EID7514In an in vitro kinase study, the recombinant PDGFRA D842V mutant kinase demonstrated sensitivity to bosutinib treatment at concentrations of 1μM and 10μM (activity %: 25 and 6) when compared to wild t… (full text at CIViC) PMID 19039322 · Remsing Rix et al., 2009 · Open in CIViC | civic |
| Gastrointestinal Stromal Tumor13 | ||||||||
| PDGFRA D842V | (diagnostic) | Diagnostic | B | Supports Negative | 3 | accepted | EID2GIST tumors harboring PDGFRA D842V mutation are more likely to be benign than malignant. PMID 15146165 · Lasota et al., 2004 · Open in CIViC | |
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
- 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 |
|---|---|---|---|---|---|---|---|---|
| 13543 | Conflicting classifications of pathogenicity | no assertion criteria provided | 0 | Gastrointestinal stromal tumor; Primary intracranial sarcoma, DICER1-mutant; Diffuse midline glioma, H3 K27M-mutant | somatic | 4 | Dec 01, 2006 | clinvar |