SLC2A1 NM_006516.4(SLC2A1):c.588G>A (p.Pro196=)

CI-VAR-00018228Explore in graph →p.Pro196=NM_006516.4:c.588G>AClinVar 95414 rs2229682

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
95414	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Dystonia 9; Encephalopathy due to GLUT1 deficiency; GLUT1 deficiency syndrome 1, autosomal recessive; Inborn genetic diseases; Hereditary cryohydrocytosis with reduced stomatin; Childhood onset GLUT1 deficiency syndrome 2; Epilepsy, idiopathic generalized, susceptibility to, 12; Uterine carcinosarcoma; Malignant lymphoma, large B-cell, diffuse	germline	19	Feb 04, 2026	clinvar