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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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364824 SNVs 1 of 36483 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010043964678 chr10: 750 CE4 Intergenic C T
heterozygote
MACSNP010043964716 chr10: 2836 CE4 Intergenic T A
homozygote
MACSNP010043964724 chr10: 3691 CE4 Intergenic T C
heterozygote
MACSNP010043964742 chr10: 4256 CE4 Intergenic A G
heterozygote
MACSNP010043964743 chr10: 4262 CE4 Intergenic G A
heterozygote
MACSNP010043964746 chr10: 4280 CE4 Intergenic A G
heterozygote
MACSNP010043964748 chr10: 4298 CE4 Intergenic G T
heterozygote
MACSNP010043964763 chr10: 4798 CE4 Intergenic G A
homozygote
MACSNP010043964778 chr10: 5315 CE4 Intergenic G A
heterozygote
MACSNP010043964826 chr10: 6820 CE4 Intergenic C T
homozygote

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