TERT NM_198253.3(TERT):c.1569_1570delinsAA (p.Ser523_Pro524delinsArgThr) — variant · CancerIndex

Variant · Indel

TERT NM_198253.3(TERT):c.1569_1570delinsAA (p.Ser523_Pro524delinsArgThr)

CI-VAR-00282838Explore in graph →p.Ser523_Pro524delinsArgThrNM_198253.3:c.1569_1570delinsAAClinVar 2009240 rs2478407475

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
2009240	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Dyskeratosis congenita, autosomal dominant 2; Idiopathic Pulmonary Fibrosis; Dyskeratosis congenita	germline	2	Oct 03, 2025	clinvar