IFT172 NM_015662.3(IFT172):c.3401G>T (p.Arg1134Leu)

CI-VAR-00046375Explore in graph →p.Arg1134LeuNM_015662.3:c.3401G>TClinVar 252701 rs148624326

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
252701	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Short-rib thoracic dysplasia 10 with or without polydactyly; Retinitis pigmentosa 71; Melanoma; Lung cancer; Cervical cancer; Familial cancer of breast; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Gastric cancer; Uterine carcinosarcoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Colorectal cancer; Sarcoma	germline	11	Jun 01, 2026	clinvar