CACNA1S NM_000069.3(CACNA1S):c.1711G>A (p.Val571Ile)

CI-VAR-00047007Explore in graph →p.Val571IleNM_000069.3:c.1711G>AClinVar 254802 rs114191482

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
254802	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Hypokalemic periodic paralysis, type 1; Malignant hyperthermia, susceptibility to, 5; Inborn genetic diseases; Thyrotoxic periodic paralysis, susceptibility to, 1; Congenital myopathy 18	germline	11	Jan 27, 2026	clinvar