RUNX1 NM_001754.5(RUNX1):c.1267_1269delinsTGT (p.Arg423Cys) — variant · CancerIndex

Variant · Indel

RUNX1 NM_001754.5(RUNX1):c.1267_1269delinsTGT (p.Arg423Cys)

CI-VAR-00385609Explore in graph →p.Arg423CysNM_001754.5:c.1267_1269delinsTGTClinVar 3948840

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
3948840	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Inborn genetic diseases; Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	germline	2	Feb 11, 2026	clinvar