NTRK1 NM_002529.4(NTRK1):c.865C>A (p.Gln289Lys)

CI-VAR-00045843Explore in graph →p.Gln289LysNM_002529.4:c.865C>AClinVar 245652 rs137979116

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
245652	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Hereditary insensitivity to pain with anhidrosis; Inborn genetic diseases; Hereditary cancer; NTRK1-related disorder	germline	13	Mar 05, 2026	clinvar