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Table 2 The variant allele frequency (VAF) information of the representative mutations in patient original cervical cancer (F0) and cervical cancer PDX models (F2 and F3)

From: Establishment and genetically characterization of patient-derived xenograft models of cervical cancer

Gene-symbol

Variant type

cDNA

Amino acid

VAF

F0

F2

F3

F0

F2

F3

F0

F2

F3

F0

F2

F3

PLCB1

SNP

c.1977C > G

p. D659E

41.54%

58.93%

47.30%

SNP

c.2438C > G

p. P813R

35.09%

42.86%

41.51%

KMT2D

SNP

c.4129C > T

p. Q1377*

25.00%

26.92%

37.50%

LRP1B

SNP

c.6688G > C

p. D2230H

26.67%

33.33%

40.00%

NAV3

DEL

c.6134del

p. N2045Tfs*7

23.53%

52.63%

44.44%

TP53

SNP

c.796G > T

p. G266*

69.57%

100.00%

100.00%

MKI67

SNP

c.7774G > C

p. E2592Q

61.90%

96.55%

100.00%

FAT1

SNP

c.9472C > T

p. R3158W

51.61%

97.22%

100.00%

PKHD1L1

SNP

c.5986G > C

p. E1996Q

18.42%

29.58%

29.73%

SPAG17

SNP

c.1314G > C

p. E438D

31.82%

42.86%

57.14%

KIAA1109

SNP

c.763G > T

p. E255*

72.41%

92.31%

100.00%