Variant · Snv
PDGFRA T674I
CI-VAR-00004335Explore in graph →NP_006197.1:p.Thr674IleNM_006206.5:c.2021C>TClinVar 13550 CIViC 577 rs121908587
Curated evidence
Evidence by cancer (4 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
- 19212337
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Myeloid/Lymphoid Neoplasms with Eosinophilia and Tyrosine Kinase Gene Fusions4 | ||||||||
| FIP1L1::PDGFRA Fusion AND PDGFRA T674I | Dasatinib | Predictive | D | Supports Resistance | 2 | submitted | EID4420In an in vitro study, a Ba/F3 cell line stably expressing the T674I mutation in the PDGFRA portion of the FIPL1-PDGFRA fusion protein was found to have reduced sensitivity to dasatinib treatment (IC50… (full text at CIViC) PMID 19212337 · Lierman et al., 2009 · Open in CIViC | civic |
| FIP1L1::PDGFRA Fusion AND PDGFRA T674I | Imatinib | Predictive | C | Supports Resistance | 2 | accepted | EID1446A patient treated with imatinib for a FIP1L1-PDGFRA mutation relapsed during treatment. A T674I mutation in the PDGFRA split kinase domain was hypothesized to confer resistance, due to the strong evid… (full text at CIViC) PMID 12660384 · Cools et al., 2003 · | |
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 13550 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Hypereosinophilic syndrome, idiopathic, resistant to imatinib; Gastrointestinal stromal tumor; Hereditary cancer-predisposing syndrome | germline | 3 | Jul 31, 2025 | clinvar |