IFT172 NM_015662.3(IFT172):c.1685C>G (p.Thr562Ser)

CI-VAR-00072662Explore in graph →p.Thr562SerNM_015662.3:c.1685C>GClinVar 476042 rs61743977

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
476042	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Short-rib thoracic dysplasia 10 with or without polydactyly; Retinitis pigmentosa 71; Oligodontia-cancer predisposition syndrome	germline	11	Jun 01, 2026	clinvar