PTPN11 NM_002834.5(PTPN11):c.214G>A (p.Ala72Thr)

CI-VAR-00025802Explore in graph →p.Ala72ThrNM_002834.5:c.214G>AClinVar 177754 rs121918453

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
177754	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	RASopathy; Juvenile myelomonocytic leukemia; Noonan syndrome; Noonan syndrome 1; Noonan syndrome and Noonan-related syndrome; Rosette-forming glioneuronal tumor; Pilocytic astrocytoma; Low grade glioma; PTPN11-related disorder	germline/somatic	11	Oct 02, 2025	clinvar