ARHGEF40 NM_018071.5(ARHGEF40):c.1760_1771del (p.Gly587_Leu591delinsVal) — variant · CancerIndex

Variant · Deletion

ARHGEF40 NM_018071.5(ARHGEF40):c.1760_1771del (p.Gly587_Leu591delinsVal)

CI-VAR-00270438Explore in graph →p.Gly587_Leu591delinsValNM_018071.5:c.1760_1771delClinVar 1801797 rs2502666544

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
1801797	Uncertain significance	no assertion criteria provided	0	Myoepithelial tumor	somatic	1	Nov 01, 2022	clinvar