MET NM_000245.4(MET):c.948A>G (p.Ile316Met)

CI-VAR-00008232Explore in graph →p.Ile316MetNM_000245.4:c.948A>GClinVar 41629 rs35225896

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
41629	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Papillary renal cell carcinoma type 1; Hereditary cancer-predisposing syndrome; Renal cell carcinoma; Hepatocellular carcinoma; Autosomal recessive nonsyndromic hearing loss 97; Osteofibrous dysplasia; Arthrogryposis, distal, IIa 11	germline	21	Feb 03, 2026	clinvar