CNTNAP2 NM_014141.6(CNTNAP2):c.3723G>A (p.Ala1241=)

CI-VAR-00018235Explore in graph →p.Ala1241=NM_014141.6:c.3723G>AClinVar 95573 rs9648691

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
95573	Benign	criteria provided, multiple submitters, no conflicts	2	Cortical dysplasia-focal epilepsy syndrome; Inborn genetic diseases; Familial cancer of breast	germline	16	Feb 04, 2026	clinvar