STK11 NM_000455.5(STK11):c.112C>G (p.Pro38Ala)

CI-VAR-00080281Explore in graph →p.Pro38AlaNM_000455.5:c.112C>GClinVar 458014 rs1060499954

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
458014	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Peutz-Jeghers syndrome; Hereditary cancer-predisposing syndrome; Breast and/or ovarian cancer; Familial pancreatic carcinoma	germline	10	Dec 09, 2025	clinvar