COL18A1 NM_001379500.1(COL18A1):c.3532_3533del (p.Gly1178fs) — variant · CancerIndex

Variant · Deletion

COL18A1 NM_001379500.1(COL18A1):c.3532_3533del (p.Gly1178fs)

CI-VAR-00169365Explore in graph →p.Gly1178fsNM_001379500.1:c.3532_3533delClinVar 976335 rs2037488871

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
976335	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Knobloch syndrome; Knobloch syndrome 1; Cowden syndrome 1	germline	3	Sep 10, 2025	clinvar