Table 4 SNV consequence counts of WES versus WGS as determined by variant effect predictor.

From: A domestic cat whole exome sequencing resource for trait discovery

Impact

Consequence

WES (%)

WGS (%)

Common

Exclusive

Total

Common

Exclusive

Total

High

Splice acceptor

97 (97)

3 (3)

100

98 (89.9)

11 (10.1)

109

High

Splice donor

137 (97.9)

3 (2.1)

140

139 (88)

19 (12)

158

High

Start lost

63 (96.9)

2 (3.1)

65

63 (100)

0 (0)

63

High

Stop gained

237 (97.9)

5 (2.1)

242

232 (92.8)

18 (7.2)

250

High

Stop lost

35 (100)

0 (0)

35

36 (97.3)

1 (2.7)

37

High

All

569 (97.8)

13 (2.2)

582

568 (92.1)

49 (7.9)

617

Moderate

missense

43,518 (99.3)

309 (0.7)

43,827

43,419 (98.1)

821 (1.9)

44,240

Moderate

All

43,516 (99.3)

309 (0.7)

43,825

43,417 (98.1)

821 (1.9)

44,238

Low

3′ UTR

2022 (97.9)

43 (2.1)

2065

2031 (94.7)

114 (5.3)

2145

Low

5′ UTR

2458 (99.5)

13 (0.5)

2471

2459 (98.6)

35 (1.4)

2494

Low

Splice region

3938 (99.5)

21 (0.5)

3959

3923 (98.7)

50 (1.3)

3973

Low

Stop retained

60 (100)

0 (0)

60

58 (96.7)

2 (3.3)

60

Low

Synonymous

87,341 (99.6)

321 (0.4)

87,662

87,182 (98.9)

956 (1.1)

88,138

Low

All

88,584 (99.6)

336 (0.4)

88,920

88,417 (98.9)

975 (1.1)

89,392

All

All

144,012 (99.4)

834 (0.6)

144,846

143,745 (98.5)

2194 (1.5)

145,939