Sequence Mutations
Non-silent SNV
  • Exon
  • Intron
  • Missense
  • Nonsense
  • RNA Gene
  • Splice/Splice-Region
Other SNV
  • 3' UTR
  • 5' UTR
  • Silent
Indels
  • Frameshift
  • Inframe indel
Chromosomal Alterations
Copy Number Changes
  • Amplification
  • Deletion
Structural Variations
  • Deletion, Insertion, Inversion
  • Inter-/intra-chromosomal translocation
Patients appearing in...
  • BLACK indicates "Discovery Patients"
  • RED indicates "Recurrence Patients"
  • BOLD indicates mutation/lesion
  • Click on the 'Pathway, Gene Symbol or % Alt (% Alterations)' column headings to sort the data.
  • The % alteration for each Gene Symbol is calculated by identifying affected patients over total patients displayed in the matrix plot.
  • The % alteration for each Patient is calculated by identifying number of genes mutated over total genes displayed in the matrix plot.
Stop Spinner
Unreasonably Slow?
Give us feedback.

PCGP Explore - What's New

Click here to view Release Notes
Stop Spinner
Unreasonably Slow?
Give us feedback.