FANCG and colorectal carcinoma: For the CRC subgroup, only three patients were tested for a suspicion of germline variants in FANCL (c.31C>T, VAF: 41.9%, CTC: 40%), APC (c.1548 + 1G>T, VAF: 78.8%, CTC: 30%), and FANCG (c.313G>6, VAF: 53.4%, CTC: 30%) genes; however, no hereditary syndrome was confirmed in the first two cases.