| | | Single nucleotide variant (intron variant) | KRT10-related condition | |
| | | Single nucleotide variant (synonymous variant) | KRT10-related condition | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | KRT10, KRT10-AS1
+1 more (V312A) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | KRT10, KRT10-AS1
+1 more (R245H) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | KRT10, KRT10-AS1
+1 more (V248M) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (splice donor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | KRT10-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KRT10-AS1, LOC126862559
+1 more (R333C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Epidermolytic hyperkeratosis 2A, autosomal dominant +1 more | |
| | KRT10, KRT10-AS1
+1 more (A409T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KRT10, KRT10-AS1
+1 more (Q403H) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Annular epidermolytic ichthyosis | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Variation (no sequence alteration) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (splice donor variant) | Congenital reticular ichthyosiform erythroderma | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Congenital reticular ichthyosiform erythroderma | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (inframe_insertion) | Bullous ichthyosiform erythroderma +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (missense variant) | KRT10-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (inframe_deletion) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Indel (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Insertion (frameshift variant) | Bullous ichthyosiform erythroderma | |
| | | Indel (nonsense) | not provided | |
| | | Single nucleotide variant (intron variant) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (nonsense) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (nonsense) | Bullous 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 | |
| | | Indel (missense variant) | Annular epidermolytic ichthyosis | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (missense variant) | Epidermolytic nevus +5 more | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma | |
| | | Single nucleotide variant (missense variant) | Bullous ichthyosiform erythroderma | |