PTEN NM_000314.8(PTEN):c.885_886del (p.Leu295_Cys296insTer) — variant · CancerIndex

Variant · Deletion

PTEN NM_000314.8(PTEN):c.885_886del (p.Leu295_Cys296insTer)

CI-VAR-00109426Explore in graph →p.Leu295_Cys296insTerNM_000314.8:c.885_886delClinVar 586388 rs1564568350

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
586388	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Global developmental delay; Cowden syndrome 1; Hereditary cancer-predisposing syndrome; PTEN hamartoma tumor syndrome	germline	5	Feb 26, 2025	clinvar