Table 1 Somatic point mutations in all time-point samples

From: Erratum: Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis

Chromosome

Position

Reference

Observed

Gene

Exonic function

AAChange

016-T00

016-T02

016-T05

016-T11

1

78425887

G

A

FUBP1

stopgain SNV

NM_003902:c.C1558T:p.Q541X

+

+

+

+

1

186277552

A

G

PRG4

nonsynonymous SNV

NM_001127710:c.A2299G:p.T901A

+

+

+

+

3

141163154

C

T

ZBTB38

nonsynonymous SNV

NM_001080412:c.C1924T:p.P643S

+

+

+

+

6

44230329

C

A

NFKBIE

stopgain SNV

NM_004556:c.G853T:p.E285X

+

6

132892234

A

C

TAAR6

nonsynonymous SNV

NM_175067:c.A774C:p.K258N

+

+

+

+

6

146264389

T

C

SHPRH

nonsynonymous SNV

NM_001042683:c.A2128G:p.M710V

+

+

+

+

11

108114749

G

C

ATM

nonsynonymous SNV

NM_000051:c.G566C:p.R189T

+

+

+

+

12

21358921

C

A

SLCO1B1

nonsynonymous SNV

NM_006446:c.C1451A:p.P484H

+

+

+

+

15

45409873

A

G

DUOXA1

nonsynonymous SNV

NM_144565:c.T1292C:p.V431A

+

+

+

+

16

745751

T

C

FBXL16

nonsynonymous SNV

NM_153350:c.A806G:p.N269S

+

+

+

+

17

42463002

G

A

ITGA2B

nonsynonymous SNV

NM_000419:c.C491T:p.A164V

+

+

+

+

19

19431945

G

A

MAU2

splicing site

NA

+

+

+

+

19

56173950

A

T

U2AF2

nonsynonymous SNV

NM_001012478:c.A569T:p.Q190L

+

+

+

X

125299321

C

A

DCAF12L2

nonsynonymous SNV

NM_001013628:c.G587T:p.W196L

+

+

+

+

  1. +, present; −, absent.