RASA1 NM_002890.3(RASA1):c.656C>G (p.Ser219Ter)

CI-VAR-00074730Explore in graph →p.Ser219TerNM_002890.3:c.656C>GClinVar 464870 rs1554044823

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
464870	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Basal cell carcinoma, susceptibility to, 1; Capillary malformation-arteriovenous malformation 1; Capillary malformation-arteriovenous malformation syndrome	germline	2	Jul 03, 2025	clinvar