COL9A3 NM_001853.4(COL9A3):c.909G>A (p.Pro303=)

CI-VAR-00047847Explore in graph →p.Pro303=NM_001853.4:c.909G>AClinVar 258437 rs2249903

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
258437	Benign	criteria provided, multiple submitters, no conflicts	2	Epiphyseal dysplasia, multiple, 3; Uterine carcinosarcoma; Colorectal cancer	germline	13	May 08, 2026	clinvar