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. 2022 Aug 3;6(21):5732–5736. doi: 10.1182/bloodadvances.2022007803

Table 1.

Results from the TruSight Myeloid Sequencing Panel for each participant at each time point evaluated after GT

Patient ID Age at GT (mo) Time point after GT (mo) Variant detected (pos/neg) Variant/description VAF, %
401 184 0 Negative
12 Negative
48 Negative
72 Negative
402 4 0 Positive KIT- VUS c.1700A>G (p.N567S) 50
120 Positive KIT- VUS c.1700A>G (p.N567S) 50
404 3 0 Positive KIT- VUS c.1700A>G (p.N567S) 49
96 Positive KIT- VUS c.1700A>G (p.N567S) 49
405 8 0 Negative
48 Negative
96 Negative
407 14 60 Negative
408 3 48 Negative
409 20 0 Negative
84 Negative
410 3 36 Positive TP53- LB c.1015G>A (p.E339K) 48
Controls ×5 N/A N/A Negative

LB, likely benign; VUS, variant of uncertain significance; N/A, not applicable.

0, baseline sample before exposure to busulfan.

Sibling donor.