COL9A3 NM_001853.4(COL9A3):c.307C>T (p.Arg103Trp)

CI-VAR-00006455Explore in graph →p.Arg103TrpNM_001853.4:c.307C>TClinVar 17139 rs61734651

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
17139	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Intervertebral disc disease, susceptibility to; Connective tissue disorder; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Uveal melanoma; Stickler syndrome; Colorectal cancer; Uterine carcinosarcoma; Thymoma; Cholangiocarcinoma; Adrenocortical carcinoma, hereditary	germline	15	May 09, 2026	clinvar