STK11 NM_000455.5(STK11):c.892_903dup (p.Arg301_Gln302insPheSerIleArg) — variant · CancerIndex

Variant · Insertion

STK11 NM_000455.5(STK11):c.892_903dup (p.Arg301_Gln302insPheSerIleArg)

CI-VAR-00257670Explore in graph →p.Arg301_Gln302insPheSerIleArgNM_000455.5:c.892_903dupClinVar 1765130 rs2512946630

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
1765130	Uncertain significance	criteria provided, single submitter	1	Hereditary cancer-predisposing syndrome	germline	1	Oct 09, 2017	clinvar