KIDINS220 NM_020738.4(KIDINS220):c.3323A>G (p.Asn1108Ser) — variant · CancerIndex

Variant · Snv

KIDINS220 NM_020738.4(KIDINS220):c.3323A>G (p.Asn1108Ser)

CI-VAR-00127850Explore in graph →p.Asn1108SerNM_020738.4:c.3323A>GClinVar 712924 rs145408226

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
712924	Likely benign	criteria provided, multiple submitters, no conflicts	2	Inborn genetic diseases; Thyroid cancer, nonmedullary, 1; Nonpapillary renal cell carcinoma	germline	5	Jul 01, 2026	clinvar