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. 2011 May 9;208(5):901–908. doi: 10.1084/jem.20110580

Table I.

Patients with B cell precursor ALL and somatic mutations in IL7R

ID IL7R mutation DNA IL-7R mutation protein CRLF2 JAK2 Gender Age at Dx WBC/liter Events
yr
DS46 c.819 Ins 12 243 InsPPCL P2RY8-CRLF2 mut M 4.9 30.5 × 109 first CCR
DS92 c.642 A>T S185C IGHα translocation WT M 15.1 112.8 × 109 first CCR
M90 c.828 Ins7 Del T 246 InsKCH P2RY8-CRLF2 WT M 1.7 123 × 109 relapse
M112 c.642 A>T S185C P2RY8-CRLF2 mut F 14.3 9.7 × 109 relapse
M117 c.814 Ins13 Del A 241 InsFSCGP P2RY8-CRLF2 mut F 10.3 7 × 109 first CCR
M122 c.642 A>T S185C P2RY8-CRLF2 WT M 7.0 7.3 × 109 relapse
M124 c.820 Ins10 Del C 244 InsCHL High expression WT M 4.9 8.9 × 109 first CCR
M223 c.642 A>T S185C P2RY8-CRLF2 WT M 8.0 27 × 109 first CCR
M61 c.820 ins21 244 InsPPVCSVT CRLF2 not expressed WT M 10.7 152 × 109 relapse

DS, Down syndrome; M, male; F, female; mut, mutated at JAK2 R683; CCR, continuous complete remission; Dx, Diagnosis; Del, Deletion; Ins, Insertion; WBC, white blood cells count.