FGFR3 NM_000142.5(FGFR3):c.393G>A (p.Ser131=)

CI-VAR-00033087Explore in graph →p.Ser131=NM_000142.5:c.393G>AClinVar 211004 rs55662109

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
211004	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Connective tissue disorder; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Hepatocellular carcinoma; Adrenocortical carcinoma, hereditary; Clear cell carcinoma of kidney; Cervical cancer; Colon adenocarcinoma; Lung cancer	germline	15	Mar 01, 2026	clinvar