PTPN11 NM_002834.5(PTPN11):c.1492C>T (p.Arg498Trp)

CI-VAR-00008014Explore in graph →p.Arg498TrpNM_002834.5:c.1492C>TClinVar 40553 rs397507541

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
40553	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	RASopathy; LEOPARD syndrome 1; Noonan syndrome 1; Noonan syndrome with multiple lentigines; Noonan syndrome; Noonan syndrome and Noonan-related syndrome; Juvenile myelomonocytic leukemia; Metachondromatosis; Cardiovascular phenotype; PTPN11-related disorder; Diffuse midline glioma, H3 K27M-mutant	germline/somatic	31	Apr 09, 2026	clinvar