TRNT1 NM_182916.3(TRNT1):c.482-3dup

CI-VAR-00066737Explore in graph →NM_182916.3:c.482-3dupClinVar 420888 rs766154756

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
420888	Likely benign	criteria provided, multiple submitters, no conflicts	2	Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome; TRNT1-related disorder; Chronic lymphocytic leukemia/small lymphocytic lymphoma	germline	6	Jan 27, 2026	clinvar