KRAS NM_004985.5(KRAS):c.27_28insCTC (p.Val9_Gly10insLeu) — variant · CancerIndex

Variant · Insertion

KRAS NM_004985.5(KRAS):c.27_28insCTC (p.Val9_Gly10insLeu)

CI-VAR-00242246Explore in graph →p.Val9_Gly10insLeuNM_004985.5:c.27_28insCTCClinVar 1711011 rs2548933366

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
1711011	Uncertain significance	no assertion criteria provided	0	Prostate cancer, hereditary, 1	germline	1	Jul 29, 2022	clinvar