C2CD3 NM_001286577.2(C2CD3):c.3911-2A>T

CI-VAR-00024901Explore in graph →NM_001286577.2:c.3911-2A>TClinVar 144040 rs149366137

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
144040	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Orofaciodigital syndrome type 14; Malignant tumor of urinary bladder; Fetal anomalies with a likely genetic cause	germline	5	Feb 03, 2026	clinvar