DNAJB2 NM_006736.6(DNAJB2):c.571C>T (p.Arg191Trp)

CI-VAR-00072563Explore in graph →p.Arg191TrpNM_006736.6:c.571C>TClinVar 473304 rs776893562

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
473304	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Neuronopathy, distal hereditary motor, autosomal recessive 5; Inborn genetic diseases; Uterine corpus endometrial carcinoma; Malignant lymphoma, large B-cell, diffuse	germline	5	Dec 14, 2025	clinvar