ARHGAP20 NM_001384657.1(ARHGAP20):c.2998G>A (p.Gly1000Arg) — variant · CancerIndex

Variant · Snv

ARHGAP20 NM_001384657.1(ARHGAP20):c.2998G>A (p.Gly1000Arg)

CI-VAR-00342119Explore in graph →p.Gly1000ArgNM_001384657.1:c.2998G>AClinVar 3128566 rs199551649

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
3128566	Uncertain significance	criteria provided, single submitter	1	Familial cancer of breast	germline	2	Apr 02, 2025	clinvar