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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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436789 SNVs 1 of 43679 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010060569765 chr15: 32286 CE4 Intergenic A C
homozygote
MACSNP010060569809 chr15: 34064 CE4 Intergenic T G
heterozygote
MACSNP010060569810 chr15: 34073 CE4 Intergenic T G
heterozygote
MACSNP010060569812 chr15: 34093 CE4 Intergenic G A
heterozygote
MACSNP010060569815 chr15: 34131 CE4 Intergenic G A
heterozygote
MACSNP010060569871 chr15: 36140 CE4 Intergenic A C
homozygote
MACSNP010060569882 chr15: 36589 CE4 Intergenic T C
homozygote
MACSNP010060569886 chr15: 36638 CE4 Intergenic G C
homozygote
MACSNP010060569891 chr15: 36724 CE4 Intergenic A G
homozygote
MACSNP010060569896 chr15: 36858 CE4 Intergenic G A
homozygote

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