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Table 2 Distribution of types of effects of the variants predicted by snpEff, a complete list is found in Table S1

From: Genetic diversity and recent ancestry based on whole-genome sequencing of endangered Swedish cattle breeds

Type

Count

Percent

Disruptive inframe deletion

1,340

0.00%

Disruptive inframe insertion

823

0.00%

Exon loss variant

8

0.00%

Frameshift variant

6,321

0.02%

Missense variant

128,377

0.36%

Splice acceptor variant

6,472

0.02%

Splice donor variant

4,356

0.01%

Splice region variant

34,945

0.10%

Intron variant

16,382,594

46.29%

other

18,828,998

53.20%

Total

35,394,234

100%