GATA2 NM_032638.5(GATA2):c.1166_1181delinsCATG (p.Lys389_Gln394delinsThrTrp) — variant · CancerIndex

Variant · Indel

GATA2 NM_032638.5(GATA2):c.1166_1181delinsCATG (p.Lys389_Gln394delinsThrTrp)

CI-VAR-00167448Explore in graph →p.Lys389_Gln394delinsThrTrpNM_032638.5:c.1166_1181delinsCATGClinVar 966897 rs2068625186

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
966897	Uncertain significance	criteria provided, single submitter	1	Deafness-lymphedema-leukemia syndrome; Monocytopenia with susceptibility to infections	germline	1	Oct 23, 2019	clinvar