IFT172 NM_015662.3(IFT172):c.1522C>T (p.Arg508Cys)

CI-VAR-00164927Explore in graph →p.Arg508CysNM_015662.3:c.1522C>TClinVar 961445 rs371011000

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
961445	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Retinitis pigmentosa 71; Short-rib thoracic dysplasia 10 with or without polydactyly; IFT172-related disorder; Inborn genetic diseases; Bardet-Biedl syndrome 20; Melanoma	germline	6	Sep 01, 2025	clinvar