TGM6 NM_198994.3(TGM6):c.789G>A (p.Lys263=)

CI-VAR-00054721Explore in graph →p.Lys263=NM_198994.3:c.789G>AClinVar 337911 rs6114033

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
337911	Benign	criteria provided, multiple submitters, no conflicts	2	Spinocerebellar ataxia type 35; Colorectal cancer	germline	9	Jan 28, 2026	clinvar