Table 3.

Common alterations seen with progression of SAMD9/9L syndrome

EventFrequency (Pastor et al15)Frequency (Wong et al16)
Chromosome alterations   
Monosomy 7 86% 58% 
Del7q 14% 11% 
UPD7q 29% 16% 
Potential revertant
SAMD9/L mutations 
29% 63% 
Somatic mutations SETBP1 RUNX1 
 EZH2 SETBP1 
 KRAS CBL 
 RUNX1 BRAF 
  KRAS 
  ETV6 
EventFrequency (Pastor et al15)Frequency (Wong et al16)
Chromosome alterations   
Monosomy 7 86% 58% 
Del7q 14% 11% 
UPD7q 29% 16% 
Potential revertant
SAMD9/L mutations 
29% 63% 
Somatic mutations SETBP1 RUNX1 
 EZH2 SETBP1 
 KRAS CBL 
 RUNX1 BRAF 
  KRAS 
  ETV6 

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