PRC1 NM_003981.3(PRC1):c.1351-124_1351-123insoAC068831.17:g.63209_63266 — variant · CancerIndex

Variant · Insertion

PRC1 NM_003981.3(PRC1):c.1351-124_1351-123insoAC068831.17:g.63209_63266

CI-VAR-00025036Explore in graph →NM_003981.3:c.1351-124_1351-123insoAC068831.17:g.63209_63266ClinVar 157647

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
157647	Uncertain significance	no assertion criteria provided	0	Familial cancer of breast	germline	1	Feb 01, 2014	clinvar