<p>This study investigated the contribution of germline genetic variants in protein-coding genes in carfilzomib-related cardiovascular adverse events among patients with multiple myeloma using whole-exome sequencing (WES) analysis. We analyzed 247 patients with multiple myeloma who had been treated with carfilzomib at the Moffitt Cancer Center. We identified a missense mutation in the <a href="https://www.ncbi.nlm.nih.gov/gene/9168">TMSB10</a>/<a href="https://www.ncbi.nlm.nih.gov/gene/129293">TRABD2A</a> locus that appeared to be associated with a higher risk for cardiovascular adverse events in these patients. In this submission, we will provide all the genotype data along with the phenotype data of whether or not a patient developed cardiovascular adverse events after carfilzomib treatment and all the covariates used in this analysis.</p>

Whole Exome Sequencing Analysis of Carfilzomib-Related Cardiotoxicity in    Multiple Myeloma Patients

14 variables across Demographics, Race and Ethnicity

Whole Exome Sequencing Analysis of Carfilzomib-Related Cardiotoxicity in Multiple Myeloma Patients

Demographics (2)

Race and Ethnicity (1)

Other (11)