MFSD6 and Lynch syndrome: We detected the MMR2 signature in tumors of four patients (PT_0SPKM4S8, PT_3CHB9PK5, PT_JNEV57VK, and PT_VTM2STE3) diagnosed with either constitutional mismatch repair deficiency (CMMRD) or Lynch syndrome (Table 2), genetic predisposition syndromes caused by a variant in a mismatch repair gene such as PMS2, MLH1, MSH2, MSH6, or others.52