| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CBFA2T3, LOC101927793 (R284W +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (R280Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (R363W +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (R358H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (H266Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (P254L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (P338L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (K230Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (P222L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CBFA2T3, LOC101927793 (T209M +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | CBFA2T3, LOC101927793 (G205S +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
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