ERG NM_182918.4(ERG):c.571_572insGGA (p.His191delinsArgAsn) — variant · CancerIndex

Variant · Insertion

ERG NM_182918.4(ERG):c.571_572insGGA (p.His191delinsArgAsn)

CI-VAR-00302288Explore in graph →p.His191delinsArgAsnNM_182918.4:c.571_572insGGAClinVar 2580269 rs2517045861

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
2580269	Uncertain significance	criteria provided, single submitter	1	Acute lymphoid leukemia	somatic	1	Sep 23, 2023	clinvar