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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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299792 SNVs 1 of 29980 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006060569676 chr15: 14047 JM2 Intergenic G A
homozygote
MACSNP006060569781 chr15: 32600 JM2 Intergenic G A
heterozygote
MACSNP006060569783 chr15: 32671 JM2 Intergenic G A
homozygote
MACSNP006060569784 chr15: 32697 JM2 Intergenic C A
homozygote
MACSNP006060569785 chr15: 32721 JM2 Intergenic T C
homozygote
MACSNP006060569886 chr15: 36638 JM2 Intergenic G C
homozygote
MACSNP006060569888 chr15: 36677 JM2 Intergenic C T
heterozygote
MACSNP006060569891 chr15: 36724 JM2 Intergenic A G
homozygote
MACSNP006060569893 chr15: 36788 JM2 Intergenic G C
homozygote
MACSNP006060569898 chr15: 37107 JM2 Intergenic G A
homozygote

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