CHEK2 NM_007194.4(CHEK2):c.992_999delinsGCTT (p.Met331fs) — variant · CancerIndex

Variant · Indel

CHEK2 NM_007194.4(CHEK2):c.992_999delinsGCTT (p.Met331fs)

CI-VAR-00303410Explore in graph →p.Met331fsNM_007194.4:c.992_999delinsGCTTClinVar 2584141 rs2517847375

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
2584141	Pathogenic	criteria provided, single submitter	1	Familial cancer of breast	unknown	1	Jun 27, 2023	clinvar