BAP1 NM_004656.4(BAP1):c.1201_1212del (p.Tyr401_Asp404del) — variant · CancerIndex

Variant · Deletion

BAP1 NM_004656.4(BAP1):c.1201_1212del (p.Tyr401_Asp404del)

CI-VAR-00059915Explore in graph →p.Tyr401_Asp404delNM_004656.4:c.1201_1212delClinVar 412428 rs776606194

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
412428	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	BAP1-related tumor predisposition syndrome; Hereditary cancer-predisposing syndrome; BAP1-related disorder; Melanoma, uveal, susceptibility to, 2; Kury-Isidor syndrome; Neoplasm; Hereditary cancer	germline/somatic	12	Jan 20, 2026	clinvar