TINF2 NM_001099274.3(TINF2):c.936C>A (p.Tyr312Ter)

CI-VAR-00049553Explore in graph →p.Tyr312TerNM_001099274.3:c.936C>AClinVar 280299 rs201677741

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
280299	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Dyskeratosis congenita; Hoyeraal-Hreidarsson syndrome; Dyskeratosis congenita, autosomal dominant 3; Revesz syndrome; Dyskeratosis congenita, autosomal dominant 1	germline	5	Dec 29, 2025	clinvar