CDKN2A NM_000077.5(CDKN2A):c.381_393delinsGATGCG (p.Arg128fs) — variant · CancerIndex

Variant · Indel

CDKN2A NM_000077.5(CDKN2A):c.381_393delinsGATGCG (p.Arg128fs)

CI-VAR-00075748Explore in graph →p.Arg128fsNM_000077.5:c.381_393delinsGATGCGClinVar 463503 rs1554653915

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
463503	Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Familial melanoma; Hereditary cancer-predisposing syndrome	germline	2	Apr 02, 2026	clinvar