TP53 NM_000546.6(TP53):c.766_770delinsCAGGTCAGGACATCCA (p.Thr256fs) — variant · CancerIndex

Variant · Indel

TP53 NM_000546.6(TP53):c.766_770delinsCAGGTCAGGACATCCA (p.Thr256fs)

CI-VAR-00042081Explore in graph →p.Thr256fsNM_000546.6:c.766_770delinsCAGGTCAGGACATCCAClinVar 231331 rs876659098

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
231331	Pathogenic	criteria provided, single submitter	1	Hereditary cancer-predisposing syndrome	germline	1	Apr 03, 2015	clinvar