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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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383460 SNVs 1 of 38346 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP008043964708 chr10: 1577 CE2 Intergenic G A
heterozygote
MACSNP008043964709 chr10: 1586 CE2 Intergenic A G
heterozygote
MACSNP008043964710 chr10: 1610 CE2 Intergenic C G
heterozygote
MACSNP008043964711 chr10: 1648 CE2 Intergenic G A
heterozygote
MACSNP008043964713 chr10: 2295 CE2 Intergenic T A
homozygote
MACSNP008043964714 chr10: 2452 CE2 Intergenic T G
heterozygote
MACSNP008043964716 chr10: 2836 CE2 Intergenic T A
homozygote
MACSNP008043964719 chr10: 3416 CE2 Intergenic C A
heterozygote
MACSNP008043964763 chr10: 4798 CE2 Intergenic G A
homozygote
MACSNP008043964770 chr10: 5026 CE2 Intergenic C T
heterozygote

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