Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype: genes and variants

Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype is linked to 1 analyzed protein (TP53). 1 DNA variants are known to cause it; 6 more are uncertain, and 0 of those already look disease-causing on computable evidence.

Last updated 2026-09-30. Research information, not medical advice.

Genes linked to Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype

Weakly linked (only a few uncertain records): PIK3CA, FANCA, PDGFRA, FBXW7, FGFR3, IDH1, PMS2, POLE and 2 more.

Known disease-causing variants in Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype

VariantPositionProtein partClinical label
TP53 R282W282DNA bindingDisease-causing (★★)

Same protein, different disease

Diseases related to Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype

Frequently asked questions

Which genes are linked to Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype?

In CATVariant, Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype is linked to 1 analyzed protein: TP53 (Cellular tumor antigen p53).

How many genetic variants are linked to Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype?

16 variants: 1 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 6 are of uncertain significance or have conflicting reports.

Which uncertain variants in Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype look disease-causing?

None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.

About this data

Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.

Download every variant as CSV · Browse all diseases · Methods · About the Center