| | | Single nucleotide variant (intron variant) | Porcupine man +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Epidermolytic hyperkeratosis 2A, autosomal dominant +1 more | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma +3 more | |
| | | Single nucleotide variant (missense variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Indel (frameshift variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Deletion (splice donor variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Congenital reticular ichthyosiform erythroderma | |
| | | Microsatellite (inframe_insertion) | KRT10-related disorder +4 more | |
| | | Microsatellite (inframe_insertion) | Congenital reticular ichthyosiform erythroderma +3 more | |
| | | Duplication (frameshift variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Duplication (inframe_insertion) | KRT10-related disorder +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Deletion (frameshift variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Duplication (frameshift variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Single nucleotide variant (splice donor variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Congenital reticular ichthyosiform erythroderma | |
| | | Single nucleotide variant (missense variant) | KRT10-related disorder +5 more | |