IFT140 NM_014714.4(IFT140):c.1010-1G>A

CI-VAR-00049565Explore in graph →NM_014714.4:c.1010-1G>AClinVar 280884 rs770185023

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
280884	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Jeune thoracic dystrophy; Saldino-Mainzer syndrome; Retinitis pigmentosa 80; Retinitis pigmentosa; Inborn genetic diseases; Acute myeloid leukemia; IFT140-related disorders	germline	10	Oct 09, 2025	clinvar