FigureĀ 4.
Mutation patterns and effect on all Tier 1 genes. Genes in Tier 1 on any of the FL, DLBCL, or BL lists are shown. Because genes can exist in >1 list and may not be assigned the same tier, the tier for each entity is indicated on the right (Tier 1, green; Tier 2, yellow; Tier 3, amber). The heat map shows the proportion of cases with mutations in that gene is shown above each entity with deeper red indicating a higher incidence. Genes known to be affected by aberrant somatic hypermutation (aSHM) are indicated with a gray rectangle to the right. The existence of functional data is indicated on the far right. The color shows whether mutations have been functionally determined to represent a loss of function (violet), gain of function (red), or neomorph (yellow). The studies demonstrating this result for these genes are as follows: ARID1A,68ID3,51TCF3,51CCND3,51FOXO1,69GNA13,59S1PR2,59RHOA,59P2RY8,59KMT2D,70,71SMARCA4,72BCL6,73BCL7A,74DDX3X,66FBXO11,75TFAP4,76CREBBP,77,78EP300,28EZH2,79,80IRF8,81PIM1,82BTG1,83,84CDKN2A,85CD79B,86DTX1,87NOTCH1,43POU2AF1,88POU2F2,89B2M, CD58,47BCL10,90CARD11,25FAS,91RRAGC,60ATP6V1B2,60ATP6AP1,60STAT6,92TBL1XR1,93TNFAIP3,94KLHL6,95MEF2B,96SGK1,97SOCS1,98MYD88,99 and TMEM30A.100 The citations for these and all remaining genes are included in the supplemental Tables.

Mutation patterns and effect on all Tier 1 genes. Genes in Tier 1 on any of the FL, DLBCL, or BL lists are shown. Because genes can exist in >1 list and may not be assigned the same tier, the tier for each entity is indicated on the right (Tier 1, green; Tier 2, yellow; Tier 3, amber). The heat map shows the proportion of cases with mutations in that gene is shown above each entity with deeper red indicating a higher incidence. Genes known to be affected by aberrant somatic hypermutation (aSHM) are indicated with a gray rectangle to the right. The existence of functional data is indicated on the far right. The color shows whether mutations have been functionally determined to represent a loss of function (violet), gain of function (red), or neomorph (yellow). The studies demonstrating this result for these genes are as follows: ARID1A,68,ID3,51,TCF3,51,CCND3,51,FOXO1,69,GNA13,59,S1PR2,59,RHOA,59,P2RY8,59,KMT2D,70,71,SMARCA4,72,BCL6,73,BCL7A,74,DDX3X,66,FBXO11,75,TFAP4,76,CREBBP,77,78,EP300,28,EZH2,79,80,IRF8,81,PIM1,82,BTG1,83,84,CDKN2A,85,CD79B,86,DTX1,87,NOTCH1,43,POU2AF1,88,POU2F2,89,B2M, CD58,47,BCL10,90,CARD11,25,FAS,91,RRAGC,60,ATP6V1B2,60,ATP6AP1,60,STAT6,92,TBL1XR1,93,TNFAIP3,94,KLHL6,95,MEF2B,96,SGK1,97,SOCS1,98,MYD88,99 and TMEM30A.100 The citations for these and all remaining genes are included in the supplemental Tables.

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