Distribution of mutations in the 62 analyzed genes in the whole series of 76 tumor samples. Analysis of genomic alterations by target sequencing panel for primary lymphomas in patients with AITL, PTCL-TFH, and PTCL-NOS. A total of 46 368,287 mapped reads were generated, and 81.8% of the total bases were aligned to the complete human genome (UCSC hg19, GRCh37, February 2009). The mean coverage was 993X (range: 31-1379) for tumor samples. Rows correspond to sequenced genes; columns represent individual PTCL patients. Color coding: blue, missense; green, synonymous; purple, frameshift; red, stop gained; yellow, splice sit; pink, UTR; orange, in frame; gray, start gained.