B3GLCT NM_194318.4(B3GLCT):c.660+1G>A

CI-VAR-00005221Explore in graph →NM_194318.4:c.660+1G>AClinVar 1264 rs80338851

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
1264	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Peters plus syndrome; B3GLCT-related disorder; Inborn genetic diseases; Thyroid cancer, nonmedullary, 1; Clear cell carcinoma of kidney; Lung cancer; Familial cancer of breast; B3GLCT-related disorders	germline	33	Jun 01, 2026	clinvar