CEP164 and ciliopathy: The first variant, (NM_014956.5 c.1726C > T; NP_055771.4:p.R576*, NM_001271933.2:c.1735C > T, NP_001258862.1:p.R579*) was a known CEP164‐ciliopathy rare allele (Table 1, Table S1), with a gnomAD allele frequency of 0.0000087, 12 (Table 1).