Table 3.
Common alterations seen with progression of SAMD9/9L syndrome
Event
.
Frequency (Pastor et al
15
)
.
Frequency (Wong et al
16
)
.
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
Event
.
Frequency (Pastor et al
15
)
.
Frequency (Wong et al
16
)
.
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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