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Table 1 PRKAR1A mutations detected within the tissues

From: Somatic PRKAR1A mutation in sporadic atrial myxoma with cerebral parenchymal metastases: a case report

  1. CCP Ion AmpliSeq™ Comprehensive Cancer Panel, CNV copy number variation, VAF variant allelic fraction, WES whole exome sequencing. Read depth is the total number of reads covering the site of the mutation, except for the amplification, for which read depth refers to the mean read depth across the entire amplified region. The mean read depth for the amplified region in normal DNA was 107. The amplified region in both the heart and brain lesions contains PRKAR1A and the gene WIPI1
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Journal of Medical Case Reports

ISSN: 1752-1947