RUNX1 NM_001754.5(RUNX1):c.167T>C (p.Leu56Ser)

CI-VAR-00045747Explore in graph →p.Leu56SerNM_001754.5:c.167T>CClinVar 239045 rs111527738

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
239045	Benign	reviewed by expert panel	3	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1; Hereditary cancer-predisposing syndrome; Acute myeloid leukemia; RUNX1-related disorder; Inborn genetic diseases	germline/somatic	18	Jul 26, 2019	clinvar