Figure 2.

SETD1B is frequently mutated or depleted in FL and DLBCL. (A) Schematic overview illustrating SETD1B mutations in FL and DLBCL. The mutations span all functional domains of the protein, with a notable hotspot mutation resulting in a premature stop codon at amino acid 30 (H8Pfs*30). (B and C) (B) Oncoprint representation of an integrated annotation of somatic mutations and DNA copy-number changes of KMT2 family genes in 216 FL and (C) 248 DLBCL samples from MSK database. SETD1B mutations showed a propensity to co-occur with KMT2D mutations (FL, P = 0.008; DLBCL, P = 0.064). P values were calculated by two-sided Fisher Exact test. (D and E) (D) Oncoprint representation of an integrated annotation of somatic mutations and DNA copy-number changes of SETD1B and TP53 genes in 216 FL and (E) 248 DLBCL from MSK database. SETD1B mutations showed a trend (non-significant) to a mutual exclusive relationship with loss of TP53 (FL, P = 0.256; DLBCL, P = 0.126). P values were calculated by two-sided Fisher Exact test. All samples are arranged in columns with genes labeled along rows. Only samples with alterations are shown.

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