NPM1 NM_002520.7(NPM1):c.863_864insCCTG (p.Trp288fs)

CI-VAR-00006299Explore in graph →p.Trp288fsNM_002520.7:c.863_864insCCTGClinVar 14001 rs1554138189

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
14001	Pathogenic	no assertion criteria provided	0	Acute myeloid leukemia; Acute myeloid leukemia with NPM1 somatic mutations	somatic	2	Jan 20, 2005	clinvar