TNFRSF11A NM_003839.4(TNFRSF11A):c.1514C>T (p.Ala505Val)

CI-VAR-00276153Explore in graph →p.Ala505ValNM_003839.4:c.1514C>TClinVar 1895846 rs761595131

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
1895846	Uncertain significance	criteria provided, single submitter	1	Lung cancer	germline	2	Dec 22, 2025	clinvar