Single nucleotide variations and indels detected by whole transcriptome sequencing. Only the genes with a variant allele frequency (Vaf) of ≥0.30 are included.

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Table 2Single nucleotide variations and indels detected by whole transcriptome sequencing. Only the genes with a variant allele frequency (Vaf) of ≥0.30 are included.

Blood Res 2016;51:17~22 https://doi.org/10.5045/br.2016.51.1.17