| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | NPM1-related condition | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +3 more) | NPM1-related condition | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (inframe_deletion) | not specified | |
| | | Single nucleotide variant (synonymous variant) | NPM1-related condition +1 more | |
| | | Microsatellite (inframe_deletion +1 more) | NPM1-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (inframe_deletion +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +1 more | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | NPM1-related condition | |
| | | Deletion (intron variant) | NPM1-related condition | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Duplication (frameshift variant +1 more) | Myelodysplastic syndrome progressed to acute myeloid leukemia | |
| | | Insertion (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Insertion (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Insertion (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Insertion (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Insertion (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Insertion (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Insertion (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Indel (frameshift variant +1 more) | Acute myeloid leukemia with multilineage dysplasia | |
| | | Indel (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Deletion (frameshift variant +1 more) | Acute myeloid leukemia | |
| | | Deletion (non-coding transcript variant) | Acute myeloid leukemia | |
| | | Single nucleotide variant (synonymous variant +1 more) | Acute myeloid leukemia | |
| | | Deletion (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Acute myeloid leukemia | |