MEN1 NM_001370259.2(MEN1):c.1621_1622delinsGA (p.Thr541Glu) — variant · CancerIndex

Variant · Indel

MEN1 NM_001370259.2(MEN1):c.1621_1622delinsGA (p.Thr541Glu)

CI-VAR-00178016Explore in graph →p.Thr541GluNM_001370259.2:c.1621_1622delinsGAClinVar 1039393 rs1941511781

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
1039393	Uncertain significance	criteria provided, single submitter	1	Multiple endocrine neoplasia, type 1	germline	1	Aug 28, 2021	clinvar