PARN NM_002582.4(PARN):c.863dup (p.Asn288fs)

CI-VAR-00025917Explore in graph →p.Asn288fsNM_002582.4:c.863dupClinVar 190290 rs786201001

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
190290	Pathogenic	no assertion criteria provided	0	Dyskeratosis congenita, autosomal recessive 6	germline	1	May 01, 2015	clinvar