DEPDC5 NM_001242896.3(DEPDC5):c.1218-13_1218-10del

CI-VAR-00047895Explore in graph →NM_001242896.3:c.1218-13_1218-10delClinVar 264754 rs150103661

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
264754	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Epilepsy, familial focal, with variable foci 1; Familial focal epilepsy with variable foci; Malignant tumor of esophagus; Uterine corpus endometrial carcinoma	germline	7	Mar 01, 2026	clinvar