WT1 NM_024426.6(WT1):c.1020_1021delinsAC (p.His340_Ser341delinsGlnArg) — variant · CancerIndex

Variant · Indel

WT1 NM_024426.6(WT1):c.1020_1021delinsAC (p.His340_Ser341delinsGlnArg)

CI-VAR-00104990Explore in graph →p.His340_Ser341delinsGlnArgNM_024426.6:c.1020_1021delinsACClinVar 581715 rs1564975891

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
581715	Uncertain significance	criteria provided, single submitter	1	Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome; Drash syndrome	germline	1	May 30, 2018	clinvar