Molecular and clinical analysis of 126 French VHL families tested for renal involvement revealed 92 different mutations. 90 of these families had renal involvement. The p.Q203Gfs*52 (c.607_608del) germline variant of the VHL gene was detected in a family (ID 399). Member 10025 had no renal involvement. Member 10024 had unknown renal involvement. Member 8840 presented with mild renal disease. The variant was reported as c.604_605del which was mapped to c.607_608del. The paper states that this family is previously reported in PMID 12202531.