FLT3 NM_004119.3(FLT3):c.2520_2521insGGATCC (p.Ser840_Asn841insGlySer) — variant · CancerIndex

Variant · Insertion

FLT3 NM_004119.3(FLT3):c.2520_2521insGGATCC (p.Ser840_Asn841insGlySer)

CI-VAR-00006369Explore in graph →p.Ser840_Asn841insGlySerNM_004119.3:c.2520_2521insGGATCCClinVar 16271 rs398122514

Curated evidence

Evidence by cancer (0 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.

Data not yet available

No curated evidence item references this variant yet.

ClinVar

Clinical significance (1)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
16271	Pathogenic	no assertion criteria provided	0	Acute myeloid leukemia	somatic	1	Nov 01, 2002	clinvar