TERT NM_198253.3(TERT):c.1836C>G (p.Ala612=)

CI-VAR-00060442Explore in graph →p.Ala612=NM_198253.3:c.1836C>GClinVar 416316 rs34170122

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
416316	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Idiopathic Pulmonary Fibrosis; Dyskeratosis congenita, autosomal dominant 2; Acute myeloid leukemia; Dyskeratosis congenita; TERT-related disorder; Melanoma, cutaneous malignant, susceptibility to, 9	germline	6	Jan 24, 2026	clinvar