COL12A1 NM_004370.6(COL12A1):c.7633G>T (p.Gly2545Trp)

CI-VAR-00281806Explore in graph →p.Gly2545TrpNM_004370.6:c.7633G>TClinVar 2010557 rs2533181046

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
2010557	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2; Inborn genetic diseases; Thyroid cancer, nonmedullary, 1	germline	3	Oct 20, 2023	clinvar