RUNX1 NM_001754.5(RUNX1):c.586A>G (p.Thr196Ala)

CI-VAR-00169867Explore in graph →p.Thr196AlaNM_001754.5:c.586A>GClinVar 988811 rs2057541324

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
988811	Likely pathogenic	reviewed by expert panel	3	Thrombocytopenia; Abnormal bleeding; Hereditary thrombocytopenia and hematologic cancer predisposition syndrome; Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	germline	3	Jun 30, 2022	clinvar