ZFHX3 NM_006885.4(ZFHX3):c.10142_10165del (p.Arg3381_Gln3388del) — variant · CancerIndex

Variant · Deletion

ZFHX3 NM_006885.4(ZFHX3):c.10142_10165del (p.Arg3381_Gln3388del)

CI-VAR-00006510Explore in graph →p.Arg3381_Gln3388delNM_006885.4:c.10142_10165delClinVar 18167 rs727502780

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
18167	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Prostate cancer, somatic	germline/somatic	3	Apr 01, 2026	clinvar