TPP2 NM_001330588.2(TPP2):c.3144-13_3144-11del

CI-VAR-00229515Explore in graph →NM_001330588.2:c.3144-13_3144-11delClinVar 1554877 rs764336466

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
1554877	Likely benign	criteria provided, single submitter	1	Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency; Familial cancer of breast	germline	2	Feb 01, 2026	clinvar