CNTN6 NM_001289080.2(CNTN6):c.288C>T (p.Gly96=)

CI-VAR-00126316Explore in graph →p.Gly96=NM_001289080.2:c.288C>TClinVar 773864 rs61739199

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
773864	Benign	criteria provided, multiple submitters, no conflicts	2	CNTN6-related disorder; Thymoma; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Gastric cancer; Sarcoma; Uterine carcinosarcoma	germline	4	Dec 31, 2019	clinvar