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Table 2 Genes disrupted by sequence validated somatic rearrangements discovered in breast cancers

From: Gene rearrangements in hormone receptor negative breast cancers revealed by mate pair sequencing

 

Sample ID

Chr 1

Breakpoint 1

Chr 2

Breakpoint 2

Disrupted genes

      

(affected regions/breakpoint locations)

Deletion

153 T

11

106618805

 

106622567

GUCY1A2 (exon 7)

 

154 T

8

72214170

 

72217978

EYA1 (intron 7–8)

 

119 T

5

134715922

 

134720809

H2AFY (intron 2–3)

 

149 T

2

12526265

 

12528008

 
 

149 T

2

65366656

 

65369602

 
 

149 T

10

22889925

 

22892366

PIP4K2A (intron 3–4)

 

149 T

15

45915722

 

45917969

 
 

152 T

12

2130488

 

2133385

 

Inversion

120 T

2

120331908

 

120335057

PCDP1 (intron 6–7)

 

116 T

5

129549038

 

129552347

 
 

149 T

10

24436405

 

24438757

KIAA1217 (intron 2–3)

 

153 T

2

172893909

 

175831452

METAP1D (intron 1–2), CHN1 (intron 1–2)

 

116 T

3

168893755

 

170864487

MECOM (intron 2–3), TNIK (intron 12–13)

 

151 T

5

137738030

 

137744577

KDM3B (intron 11–12)

Translocation

153 T

2

42052398

4

66411362

EPHA5 (intron 3–4)

 

153 T

6

104501617

X

152223450

 
 

153 T

7

54909974

19

29832131

 
 

153 T

8

57916723

19

30951050

ZNF536 (intron 2–3)

 

153 T

12

48517177

19

30945107

PFKM (intron 3–4), ZNF536 (intron 2–3)

 

153 T

19

30355201

X

153152399

LCA10 (intron 5–6)

 

153 T

5

174245601

10

65204015

JMJD1C (intron 1–2)

 

116 T

2

199768975

5

28258969

 
 

118 T

7

90081994

17

25904801

KSR1 (intron 3–4)

 

118 T

15

60231305

21

47148999

PCBP3 (intron 1–2)

 

118 T

15

60833617

21

35917066

RCAN1 (intron 1–2), RORA (intron 2–3)

 

118 T

15

61356378

21

41870300

DSCAM (intron 3–4), RORA (intron 1–2)

 

118 T

15

61375512

21

27982153

RORA (intron 1–2)

 

118 T

15

71750638

21

18023846

THSD4 (intron 6–7)

 

119 T

2

42052196

4

66411644

EPHA5 (intron 3–4)

 

119 T

4

4714578

17

38990874

TMEM99 (exon 3)

 

119 T

8

32833459

18

64563574

 
 

120 T

8

127068558

11

112588800

 
 

120 T

11

108583473

13

21735983

DDX10 (intron 10–11), SKA3 (exon 5)

 

120 T

13

103233303

16

77586406

 
 

148 T

2

65563071

8

80378299

SPRED2 (intron 2–3)

 

148 T

9

13526912

17

57745082

CLTC (intron 13–14)

 

149 T

1

247997045

10

27944748

 
 

149 T

3

47806974

4

151298580

LRBA (intron 48–49), SMARCC1 (intron 2–3)

 

149 T

5

15946143

17

67928932

 
 

149 T

11

108583658

13

21742368

DDX10 (intron 10–11), SKA3 (exon 4)

  1. Chr 1, the lower numbered chromosome in a rearrangement; Breakpoint 1, the breakpoint position on Chr 1 determined by Sanger sequencing; Chr 2, the other chromosome in a rearrangement; Breakpoint 2, the breakpoint position on Chr 2. Chromosome coordinates are based on human genome build HG19.