| Mutation type:Deletion | Mutation effect:Frameshift | Nucleotide number:566 | |||
| Genome location:Exon7 | Subdomain:Linker | ||||
| Alpha missense prediction value:— | Alpha missense prediction class:— | ||||
| No. of patients reported: 5 | |||||
| Patient information: Monoallelic variation (5); Biallelic variation (0) | |||||
| Patient | Sex | Age | Genotype | PC: amidolytic act (%) | PC: clotting act (%) | PC: Ag (%) | PCD type | Clinical presentation (age) | First onset age | Country | Comments | Reference |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | NA | NA | hetero | 59 | 33 | 50 | I | NA | NA | Germany | NA | PMID: 7482420 |
| 2 | NA | NA | hetero | NA | NA | NA | I | NA | NA | Germany | NA | PMID: 7482420 |
| 3 | NA | NA | hetero | NA | NA | NA | I | NA | NA | Germany | NA | PMID: 7482420 |
| 4 | NA | NA | hetero | NA | NA | NA | I | NA | NA | Germany | NA | PMID: 7482420 |
| 5 | NA | NA | hetero | NA | NA | NA | I | NA | NA | Germany | NA | PMID: 7482420 |