CDKN2A NM_000077.5(CDKN2A):c.95_112del (p.Leu32_Leu37del) — variant · CancerIndex

Variant · Deletion

CDKN2A NM_000077.5(CDKN2A):c.95_112del (p.Leu32_Leu37del)

CI-VAR-00215447Explore in graph →p.Leu32_Leu37delNM_000077.5:c.95_112delClinVar 1409909 rs1819949737

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
1409909	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Familial melanoma; Hereditary cancer-predisposing syndrome; Gastric cancer; Spindle cell sarcoma; Melanoma	germline/somatic	4	Jan 26, 2024	clinvar