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. 2022 Feb 2;44(2):750–763. doi: 10.3390/cimb44020052

Table 4.

Variants per oncogene/tumor-suppressor gene that were detected in all sequenced CTCs within a subject (total number of variants per gene were combined from all seven subjects; variants detected in ≥1 subject were counted once only, adding up to a total of 598 variants).

Gene Number of Variants
NF1 69
BRCA2 33
PTCH1 33
NF2 27
ATM 25
EGFR 24
ERBB3 24
PIK3CA 19
APC 17
BRCA1 17
RB1 13
SMARCB1 13
TP53 13
CDH1 12
CSF1R 11
NOTCH1 11
SMO 11
TERT 11
ABL1 10
MLH1 10
EZH2 9
FGFR2 9
SMAD4 9
DNMT3A 8
FBXW7 8
MTOR 8
CTNNB1 7
ERBB2 7
HNF1A 7
KIT 7
PIK3R1 7
PTEN 7
ALK 6
CDKN2A 6
PTPN11 6
ERBB4 5
JAK2 5
JAK3 5
RET 5
BRAF 4
KRAS 4
LOC100507346 4
STK11 4
VHL 4
FGFR3 3
FLT3 3
HRAS 3
IDH1 3
IDH2 3
KDR 3
MET 3
NPM1 3
TSC1 3
AKT1 2
FGFR1 2
GNAQ 2
GNAS 2
NRAS 2
PDGFRA 2
ATM; C11orf65 1
FBXW7-AS1 1
GNA11 1
MAP2K1 1
MSH6 1