Table 5.

Clone features of patients with CH that developed hematologic malignancy over the course of the study

Patient IDNumber of mutationsMutationMaximum VAFHigh risk geneAverage VAFType of malignancy
0004 TET2 R1516X 0.398 No 0.217 MDS 
  TET2 Q695X 0.369 No   
  SRSF2 P95H 0.177 Yes   
  JAK2 V617F 0.02 Yes   
1060 SF3B1 R625C 0.241 Yes 0.236 MDS 
1073 TET2 Q742X 0.422 No 0.237 CMML 
  SRSF2 P95R 0.330 Yes   
  TET2 Y1245Lfs∗22 0.270 No   
  TET2 N535Kfs∗6 0.033 No   
1096 TET2 G1288D 0.796 No 0.758 CMML 
2026 TP53 Y220C 0.676 Yes 0.676 AML 
2038 TET2 Q749Rfs∗15 0.021 No 0.021 MDS 
Patient IDNumber of mutationsMutationMaximum VAFHigh risk geneAverage VAFType of malignancy
0004 TET2 R1516X 0.398 No 0.217 MDS 
  TET2 Q695X 0.369 No   
  SRSF2 P95H 0.177 Yes   
  JAK2 V617F 0.02 Yes   
1060 SF3B1 R625C 0.241 Yes 0.236 MDS 
1073 TET2 Q742X 0.422 No 0.237 CMML 
  SRSF2 P95R 0.330 Yes   
  TET2 Y1245Lfs∗22 0.270 No   
  TET2 N535Kfs∗6 0.033 No   
1096 TET2 G1288D 0.796 No 0.758 CMML 
2026 TP53 Y220C 0.676 Yes 0.676 AML 
2038 TET2 Q749Rfs∗15 0.021 No 0.021 MDS 

Clone features considered to be high-risk include total number of mutations, VAF, and mutation(s) in high-risk genes.

AML, acute myeloid leukemia; CMML, chronic myelomonocytic leukemia; MDS, myelodysplastic syndrome.

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