POLE NM_006231.4(POLE):c.1741G>T (p.Ala581Ser)

CI-VAR-00109218Explore in graph →p.Ala581SerNM_006231.4:c.1741G>TClinVar 584837 rs755090755

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
584837	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Familial colorectal cancer; Hereditary cancer-predisposing syndrome; Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency; Colorectal cancer, susceptibility to, 12; Facial dysmorphism-immunodeficiency-livedo-short stature syndrome	germline	4	Jan 31, 2026	clinvar