SLC2A1 NM_006516.4(SLC2A1):c.902C>T (p.Ala301Val)

CI-VAR-00170703Explore in graph →p.Ala301ValNM_006516.4:c.902C>TClinVar 1008366 rs1425773776

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
1008366	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	GLUT1 deficiency syndrome 1, autosomal recessive; Encephalopathy due to GLUT1 deficiency; Gastric cancer; Inborn genetic diseases	germline	4	Feb 02, 2026	clinvar