EGFR NM_005228.5(EGFR):c.474C>G (p.Asn158Lys)

CI-VAR-00242620Explore in graph →p.Asn158LysNM_005228.5:c.474C>GClinVar 1717846 rs2072454

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
1717846	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	EGFR-related lung cancer; Hereditary cancer-predisposing syndrome; Thyroid cancer, nonmedullary, 1; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma	germline	3	Mar 25, 2025	clinvar