Fig. 5: Mutational overlap with cHL and DLBCL. | Leukemia

Fig. 5: Mutational overlap with cHL and DLBCL.

From: Genetic lesions in nodular lymphocyte-predominant Hodgkin lymphoma and T cell/histiocyte-rich large B-cell lymphoma identified by whole genome sequencing

Fig. 5

Considered were all nonsynonymous SNV present in at least one case in the present study (excluding the hypermutated case 6) and/or recurrently mutated in at least one of the publications on 639 cHL patients [38,39,40,41,42] and/or 878 DLBCL patients [43, 44]. Genes that were affected by nonsynonymous SNVs in more than one case in the present study are printed in bold.

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