CDKN2A NM_000077.5(CDKN2A):c.-16GGCGGCGGGGAGCAGCATGGAGCC[1] (p.Ala4_Pro11del)

CI-VAR-00033749Explore in graph →p.Ala4_Pro11delNM_000077.5:c.-16GGCGGCGGGGAGCAGCATGGAGCC[1]ClinVar 216277 rs587780668

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
216277	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Familial melanoma; Melanoma-pancreatic cancer syndrome; Hereditary cancer-predisposing syndrome; Melanoma and neural system tumor syndrome; Melanoma, cutaneous malignant, susceptibility to, 2	germline	14	Jan 27, 2026	clinvar