FLT3 Q338E

CI-VAR-00003534Explore in graph →CIViC 5185

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.

civicCuratedShowing 1–1 of 1 evidence items across 1 cancer context on this page · levels, directions and significance as curated at the source; each row links to its CIViC record.

Molecular profile	Therapy	Type	Level	Direction · significance	Rating (1–5)	Status	Evidence	Source
Malignant Neoplasm1
FLT3 Q338E	(oncogenic)	Oncogenic	C	Does Not Support Oncogenicity	2	submitted	EID12427 The variant has been identified in the following tumors. Tumors from the AACR GENIE Project are likely somatic, but most testing was unmatched with a germline sample (https://www.aacr.org/wp-content/u… (full text at CIViC) PMID 37668528 · de Bruijn et al., 2023 · 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.