| | KRT5, LOC126861525 (R480G) | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (nonsense) | not provided | |
| | KRT5, LOC126861525 (E478K) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (E477G) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (E477K) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | KRT5, LOC126861525 (E477*) | Single nucleotide variant (nonsense) | Epidermolysis bullosa simplex 2A, generalized severe | |
| | KRT5, LOC126861525 (G476A) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (G476D) | Single nucleotide variant (missense variant) | Epidermolysis bullosa simplex 2B, generalized intermediate +2 more | |
| | KRT5, LOC126861525 (E475G) | Single nucleotide variant (missense variant) | Epidermolysis bullosa simplex 2A, generalized severe | |
| | KRT5, LOC126861525 (E475K) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (K472*) | Single nucleotide variant (nonsense) | Epidermolysis bullosa simplex 2B, generalized intermediate | |
| | KRT5, LOC126861525 (R471C) | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | KRT5, LOC126861525 (T469P) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (I467M) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (I467T) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (I467L) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (E466D) | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | KRT5, LOC126861525 (L463P) | Single nucleotide variant (missense variant) | Epidermolysis bullosa simplex +1 more | |
| | KRT5, LOC126861525 (E455fs) | Indel (frameshift variant) | not provided | |
| | KRT5, LOC126861525 (K443N) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (A438D) | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (inframe_deletion) | not provided | |
| | KRT5, LOC126861525 (A428V) | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | KRT5, LOC126861525 (A428T) | Single nucleotide variant (missense variant) | Epidermolysis bullosa simplex | |
| | KRT5, LOC126861525 (E418K) | Single nucleotide variant (missense variant) | Epidermolysis bullosa simplex 2C, localized, modifier of | |
| | KRT5, LOC126861525 (K404E) | Single nucleotide variant (missense variant) | not provided | |
| | KRT5, LOC126861525 (S387T) | Single nucleotide variant (missense variant) | not provided | |