Patient B had a 17:7576870 C > A (in GRCh37; TP53c.976 G > T) nonsense variant with a VAF of 0.22 in the tumor and a 17:7577095–7577123 deletion (in GRCh37; TP53c.815del29) in TP53 with a VAF 0.34 in the tumor. Here, TP53 is linked to neoplasm.