CASR NM_000388.4(CASR):c.1631G>A (p.Arg544Gln)

CI-VAR-00042820Explore in graph →p.Arg544GlnNM_000388.4:c.1631G>AClinVar 237758 rs115230894

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
237758	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Autosomal dominant hypocalcemia 1; Familial hypocalciuric hypercalcemia 1; Familial hypoparathyroidism; Neonatal severe primary hyperparathyroidism; Familial hypocalciuric hypercalcemia; Hereditary cancer-predisposing syndrome; Epilepsy, idiopathic generalized, susceptibility to, 8; Nephrolithiasis/nephrocalcinosis; Familial hyperparathyroidism or Hypocalciuric hypercalcaemia	germline	17	May 15, 2026	clinvar