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Table 3.

The association between the germline variant rs61757955 and genomic and histological variables

VariableMean or Percentage (Wild Type)Mean or Percentage (Mutant)P-value
CIC Mutated 15.9% 38.1% 0.017 
1p/19q Co-deletion 25.2% 47.6% 0.038 
Oligodendroglioma 33.7% 42.9% 0.475 
Total Somatic Mutation Count 30.9 30.0 0.766 
Percent Aneuploidy 15.1% 11.7% 0.524 
Astrocytoma 38.1% 42.9% 0.651 
Grade 3 53.0% 42.9% 0.497 
IDH Mutated 78.1% 85.7% 0.583 
1p/19q Co-deletion 25.2% 47.6% 0.038 
MGMT Promoter Methylation 77.8% 81.0% 1.000 
Chr 7 Gain/Chr 10 Loss 13.0% 9.5% 1.000 
Expression of GRB2 (FPKM) 45.7 44.4 0.636 
VariableMean or Percentage (Wild Type)Mean or Percentage (Mutant)P-value
CIC Mutated 15.9% 38.1% 0.017 
1p/19q Co-deletion 25.2% 47.6% 0.038 
Oligodendroglioma 33.7% 42.9% 0.475 
Total Somatic Mutation Count 30.9 30.0 0.766 
Percent Aneuploidy 15.1% 11.7% 0.524 
Astrocytoma 38.1% 42.9% 0.651 
Grade 3 53.0% 42.9% 0.497 
IDH Mutated 78.1% 85.7% 0.583 
1p/19q Co-deletion 25.2% 47.6% 0.038 
MGMT Promoter Methylation 77.8% 81.0% 1.000 
Chr 7 Gain/Chr 10 Loss 13.0% 9.5% 1.000 
Expression of GRB2 (FPKM) 45.7 44.4 0.636 

NOTE: Patients were divided based on whether or not they had the germline variant rs61757955. Patients with the germline variant rs61757955 were more likely (p < 0.05) to have CIC-mutated gliomas and the 1p/19q codeletion (bold).

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