DDX41 NM_016222.4(DDX41):c.415_418dup (p.Asp140delinsGlyTer) — variant · CancerIndex

Variant · Insertion

DDX41 NM_016222.4(DDX41):c.415_418dup (p.Asp140delinsGlyTer)

CI-VAR-00033091Explore in graph →p.Asp140delinsGlyTerNM_016222.4:c.415_418dupClinVar 210843 rs762890562

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
210843	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Acute myeloid leukemia; DDX41-related hematologic malignancy predisposition syndrome; DDX41-related disorder; Inborn genetic diseases; DDX41-related disorders	germline	18	Feb 12, 2026	clinvar