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. 2020 Jul;21(7):2003–2012. doi: 10.31557/APJCP.2020.21.7.2003

Table 4.

The Observed Frequency of BCR-ABL1 TKD Mutations in Different Studies

Study Method of the detection Overall frequency of
BCR-ABL1 mutations (%)
Common hotspot BCR-ABL1 TKD mutations (%) CML phases
This study
(Thai study)
Direct sequencing 20 (49/245) Single mutation (13)
Q252H (0.4)            F317L (1)
Y253H (0.4)            A350T (0.4)
E255K (2)            F359I/V (1)
D276G (0.4)            E455K (0.4)
F311I (0.4)            E459K (0.4)
T315I (7)            F486S (0.4)
Compound/polyclonal mutations (7)
NA
Elias et al., (2014 )(Malaysian study)
(Elias et al., 2014)
D-HPLC and Direct sequencing 22 (28/125) Single mutation
G250E (2)            M351T (2)
G251E (1)            E355A/G (2)
Y253H (1)            F359C (2)
E255K (4)            N368S (1)
D276G (1          L387M (1)
V289F (1)            H396R (1)
T315I (7)            A397P (1)
Compound/polyclonal mutation (NA)
CP,AP,BP
Meggyesi et al., (2012) Direct sequencing 20 (15/74) Single mutation CP,AP,BP, Ph positive ALL
(Hungarian study)
(Meggyesi et al., 2012)
M244K/V (8)           M351T (5)
G250E (1)            E355G (1)
Y253H (1)            F359I/V (3)
E255V (4)            L384M (1)
D276G (1)            L387M (1)
E279K (1)            H396R (1)
T315I (5)
Compound/polyclonal mutation (NA)
Kim et al., (2009) (Korean syudy)
(Kim et al., 2009)
Direct sequencing and ASO-PCR 51 (70/137) Single mutation
M244V (9)          E355G (1)
G250E (10)           F359C (1)
Q252H (4)            F359I/V (5)
Y253F/H (14)           H396P/R (2)
E255K/V (17)           S417Y (1)
T315I (23)            E450K (1)
F317L (4)            E459K (4)
M351T (2)            P480L (1)
Compound/polyclonal mutation (NA)
CP,AP,BP
Branford et al., (2003) (Australian study)
(Branford et al., 2003)
Direct sequencing 19 (27/144) Single mutation (14)
M244V (1)            M351T (6)
L248V (1)            E355G (2)
G250E (1)            F359V (1)
Q252H (3)            H396R (1)
Y253F (1)            S417Y (1)
E255K/V (4)            E459K (1)
T315I (1)            F486S (1)
F317L (1)           
Compound/polyclonal mutations (5)
CP,AP