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. 2011 Feb;2(1):11–19. doi: 10.1177/2040620710393391

Table 1.

Summary of patients with myeloproliferative neoplasms with nonsynonymous LNK mutations.

LNK mutation Domains affected Diagnosis Study
DEL PH + SH2 PMF [Oh et al. 2010]
E208Q PH ET [Oh et al. 2010]
E208X PH + SH2 JAK2-negative erythrocytosis [Lasho et al. 2010]
A215V PH JAK2-negative erythrocytosis [Lasho et al. 2010]
A215V PH Post-PMF AML1 [Pardanani et al. 2010]
A215V PH Post-PMF AML1 [Pardanani et al. 2010]
G220R PH PMF2 [Pardanani et al. 2010]
G220V PH PMF2 [Pardanani et al. 2010]
A223V D234N PH Post-PMF AML3 [Pardanani et al. 2010]
G229S PH Post-PMF AML4 [Pardanani et al. 2010]
685–691_delGGCCCCG; 955_delA PH + SH2; SH2 PMF/AML5 PMF/AML5 [Pardanani et al. 2010]
1

Mutation not present at the chronic phase.

2

Mutation not detected at the blast phase.

3

Both mutations detected in the same patient and not present in the chronic phase.

4

Chronic phase samples not available for analysis.

5

Both deletion mutations detected in the same patient and present in both chronic and blast phases.

PH, pleckstrin homology; SH2, Src homology 2; PMF, primary myelofibrosis; ET, essential thrombocythemia; AML, acute myeloid leukemia.