MAGT1 NM_001367916.1(MAGT1):c.297C>G (p.Ile99Met)

CI-VAR-00302422Explore in graph →p.Ile99MetNM_001367916.1:c.297C>GClinVar 2582378 rs781860795

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
2582378	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Congenital disorder of glycosylation, type ICC; X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia	germline	2	Dec 24, 2023	clinvar