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Table 2 Predicted consequences of variants

From: Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation and homozygous truncating mutations

 

SNPs

Indels

Exonic SVs

Strain

Synonymous

Non-synonymous

Stop gain/loss

Frameshift variant

Inframe variant

Deletions

Insertions

BUB/BnJ

9751

6050

44

41

169

1247

720

C57BL/10J

581

298

0

4

8

57

102

C57BR/cdJ

4400

2948

18

26

52

288

227

C58/J

5238

3362

23

35

69

330

254

DBA/1J

9782

6198

39

53

149

419

389

I/LnJ

10389

6249

42

52

150

690

1671

KK/HiJ

10816

6197

50

56

140

599

462

MOLF/EiJ

33710

17,311

108

172

439

897

1305

NZB/B1NJ

10403

6367

43

62

146

500

390

NZW/LacJ

10434

6326

46

61

146

673

425

RF/J

9891

6174

39

56

140

2033

862

SEA/GnJ

9309

6027

38

57

138

1284

614

ST/bJ

9021

5578

45

59

133

713

413