STK11 NM_000455.5(STK11):c.1189_1190delinsTT (p.Ala397Leu) — variant · CancerIndex

Variant · Indel

STK11 NM_000455.5(STK11):c.1189_1190delinsTT (p.Ala397Leu)

CI-VAR-00315493Explore in graph →p.Ala397LeuNM_000455.5:c.1189_1190delinsTTClinVar 2739269 rs2512954977

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
2739269	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Peutz-Jeghers syndrome; Hereditary cancer-predisposing syndrome	germline	2	Mar 08, 2025	clinvar