CACNA1D NM_001128840.3(CACNA1D):c.5296G>C (p.Ala1766Pro)

CI-VAR-00093109Explore in graph →p.Ala1766ProNM_001128840.3:c.5296G>CClinVar 504809 rs199874790

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
504809	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Sinoatrial node dysfunction and deafness; Aldosterone-producing adenoma with seizures and neurological abnormalities; Inborn genetic diseases	germline	10	Apr 13, 2026	clinvar