| | HOXA10, HOXA10-HOXA9 (P246L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (G229D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (K224E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (D176N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (G6S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (G52C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (M389I) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | HOXA10-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXA10-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXA10-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXA10-related disorder | |
| | | Deletion (inframe deletion) | HOXA10-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXA10-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXA10-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXA10-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXA10-related disorder | |
| | | Single nucleotide variant (intron variant) | HOXA10-related disorder | |
| | HOXA10, HOXA10-HOXA9 (R268Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (D198N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (P94Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (P152Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (Y7C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (A201S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (A305T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (S313L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (G221R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (D262N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (G50E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (Q138P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (R265G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (G207W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (A269S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (R268P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (G283C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (P304S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (G194D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (R248S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (Q379E) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | HOXA10-HOXA9, HOXA10 (Q140P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HOXA10, HOXA10-HOXA9 (Y57C) | Single nucleotide variant (missense variant) | not specified | |
| | HOXA10-HOXA9, HOXA10 (P122S) | Single nucleotide variant (missense variant) | HOXA10-related disorder +1 more | |