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Table 2 Mutations identified by whole-exome sequencing

From: Simulation and estimation of gene number in a biological pathway using almost complete saturation mutagenesis screening of haploid mouse cells

   

(SnpEff§) High

Moderate

Low

Modifier

Clone name

Responsible genes*

Total no. of mutations

Nonsense mutations

Splice site alterations

Frameshift mutations

Loss of start codon

Nonsynonymous mutations etc.||

Synonymous mutations

Others¶

 

B3-1

Pigt

220

6

5

0

0

115

39

1

54

B5-1

Dpm1

297

6

3

0

1

128

60

2

97

B7-2

Pigo

218

5

1

0

0

103

38

1

70

B102

Pigb

10

0

0

1

0

4

0

0

5

B201

Pigk

41

1

1

0

0

14

7

0

18

B502

Dpm1, Pigv

511

13

12

1

1

241

110

5

128

B1001

Pigv

306

8

2

0

0

127

55

1

113

B1002

Pigs

330

10

2

1

0

152

63

0

102

B1007

Gpaa1

23

1

1

0

0

9

2

1

9

F-43

Pigo

375

12

4

2

0

153

83

2

119

Average

233.1

10

104.6

47

71.5

  1. *Genes whose mutations are responsible for the host cell phenotypes.
  2. †All exons are deleted (Additional file 7: Figure S4).
  3. ‡Undetectable because of an exome design defect (Additional file 2: Figure S2).
  4. §Also explained in Additional file 6: Table S12.
  5. ||The remainder: one codon insertion in clone B102.
  6. ¶Others: start gained; synonymous stop.