NPM1 NM_002520.7(NPM1):c.864_873delinsTTTAAGGATTCGTC (p.Trp288fs) — variant · CancerIndex

Variant · Indel

NPM1 NM_002520.7(NPM1):c.864_873delinsTTTAAGGATTCGTC (p.Trp288fs)

CI-VAR-00134822Explore in graph →p.Trp288fsNM_002520.7:c.864_873delinsTTTAAGGATTCGTCClinVar 810668 rs1581263026

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
810668	Pathogenic	no assertion criteria provided	0	Acute myeloid leukemia with multilineage dysplasia	somatic	1	Jan 07, 2020	clinvar