PTPN11 NM_002834.5(PTPN11):c.854T>C (p.Phe285Ser)

CI-VAR-00006200Explore in graph →p.Phe285SerNM_002834.5:c.854T>CClinVar 13335 rs121918463

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
13335	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Noonan syndrome 1; Noonan syndrome; Early T cell progenitor acute lymphoblastic leukemia; RASopathy; Non-immune hydrops fetalis; Noonan syndrome and Noonan-related syndrome; PTPN11-related disorder; LEOPARD syndrome 1; Metachondromatosis; Autosomal dominant PTPN11-related disorders; Pilocytic astrocytoma	germline/somatic	30	Feb 01, 2026	clinvar