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. Author manuscript; available in PMC: 2021 Jun 14.
Published in final edited form as: Cancer. 2018 Dec 12;125(7):1060–1069. doi: 10.1002/cncr.31908

Figure 1.

Figure 1.

Flow chart of the study design and the filtration of pathogenic variants and variants of unknown clinical significance. Indel indicates insertion or deletion; MAF, minor allele frequency; SNP, single-nucleotide polymorphism; SNV, single-nucleotide variant.