VCP NM_007126.5(VCP):c.129+47G>A

CI-VAR-00047318Explore in graph →NM_007126.5:c.129+47G>AClinVar 260121 rs10972300

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
260121	Benign	criteria provided, multiple submitters, no conflicts	2	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1; Frontotemporal dementia and/or amyotrophic lateral sclerosis 6; Charcot-Marie-Tooth disease type 2Y; Familial cancer of breast; Malignant lymphoma, large B-cell, diffuse	germline	5	Dec 05, 2021	clinvar