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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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478593 SNVs 1 of 47860 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010040365689 chr9: 2457 CE4 Intergenic G A
homozygote
MACSNP010040365692 chr9: 2579 CE4 Intergenic T A
homozygote
MACSNP010040365703 chr9: 2893 CE4 Intergenic A G
homozygote
MACSNP010040365706 chr9: 3205 CE4 Intergenic A G
homozygote
MACSNP010040365711 chr9: 3288 CE4 Intergenic T C
heterozygote
MACSNP010040365712 chr9: 3325 CE4 Intergenic T C
homozygote
MACSNP010040365713 chr9: 3379 CE4 Intergenic G T
homozygote
MACSNP010040365720 chr9: 4206 CE4 Intergenic A C
homozygote
MACSNP010040365724 chr9: 4298 CE4 Intergenic T G
homozygote
MACSNP010040365751 chr9: 8790 CE4 Intergenic T C
homozygote

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