PRKN NM_004562.3(PRKN):c.823C>T (p.Arg275Trp)

CI-VAR-00005663Explore in graph →p.Arg275TrpNM_004562.3:c.823C>TClinVar 7050 rs34424986

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
7050	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive juvenile Parkinson disease 2; Young-onset Parkinson disease; Ovarian neoplasm; Lung carcinoma; Leprosy, susceptibility to, 2; PRKN-related disorder; Ovarian cancer; Parkinson disease 12; Lung cancer; PARK2 & PRKN-related disorders	germline	36	Jun 01, 2026	clinvar