MET NM_000245.4(MET):c.534C>T (p.Ser178=)

CI-VAR-00018146Explore in graph →p.Ser178=NM_000245.4:c.534C>TClinVar 93578 rs35775721

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
93578	Benign	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Papillary renal cell carcinoma type 1; Renal cell carcinoma; Autosomal recessive nonsyndromic hearing loss 97	germline	18	Feb 04, 2026	clinvar