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Filter SNVs Using Feature Selection

Chromosome chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20
Individual All CR1 CR2 CR3 TW1 JM1 JM2 CE1 CE2 CE3 CE4 CE5 TM1 TM2 AM1 SM1 SM2 PM1 PM2 LM1 BM1
Gene feature All CDS EXON 3'UTR INTRON 5'UTR Genotype All homozygote heterozygote Mutation All non-synonymous synonymous
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353904 SNVs 1 of 35391 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009043964665 chr10: 526 CE3 Intergenic T C
heterozygote
MACSNP009043964666 chr10: 554 CE3 Intergenic C T
heterozygote
MACSNP009043964667 chr10: 607 CE3 Intergenic C A
heterozygote
MACSNP009043964668 chr10: 614 CE3 Intergenic C T
heterozygote
MACSNP009043964669 chr10: 624 CE3 Intergenic C G
heterozygote
MACSNP009043964700 chr10: 1029 CE3 Intergenic A G
heterozygote
MACSNP009043964701 chr10: 1042 CE3 Intergenic A G
heterozygote
MACSNP009043964727 chr10: 3752 CE3 Intergenic T C
heterozygote
MACSNP009043964755 chr10: 4470 CE3 Intergenic A T
heterozygote
MACSNP009043964769 chr10: 4922 CE3 Intergenic T C
heterozygote

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