PTPN11 NM_002834.5(PTPN11):c.255C>T (p.His85=)

CI-VAR-00006933Explore in graph →p.His85=NM_002834.5:c.255C>TClinVar 36708 rs61736914

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
36708	Benign	reviewed by expert panel	3	Noonan syndrome; RASopathy; Cardiovascular phenotype; LEOPARD syndrome 1; Metachondromatosis; Noonan syndrome 1; Noonan syndrome and Noonan-related syndrome; Juvenile myelomonocytic leukemia; Hereditary cancer-predisposing syndrome	germline	20	Apr 18, 2017	clinvar