TERT NM_198253.3(TERT):c.1892G>A (p.Arg631Gln)

CI-VAR-00006720Explore in graph →p.Arg631GlnNM_198253.3:c.1892G>AClinVar 29899 rs199422294

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
29899	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Dyskeratosis congenita, autosomal dominant 2; Interstitial lung disease 2; Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1; Telomere syndrome; Idiopathic Pulmonary Fibrosis; Pulmonary fibrosis; Dyskeratosis congenita	germline	12	Feb 05, 2026	clinvar