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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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437617 SNVs 1 of 43762 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013040365693 chr9: 2583 TM2 Intergenic T C
homozygote
MACSNP013040365706 chr9: 3205 TM2 Intergenic A G
homozygote
MACSNP013040365757 chr9: 9756 TM2 Intergenic A G
homozygote
MACSNP013040365778 chr9: 13967 TM2 Intergenic A G
homozygote
MACSNP013040365784 chr9: 14224 TM2 Intergenic C T
homozygote
MACSNP013040365807 chr9: 14698 TM2 Intergenic C G
homozygote
MACSNP013040365810 chr9: 14822 TM2 Intergenic C T
homozygote
MACSNP013040365812 chr9: 14855 TM2 Intergenic G A
homozygote
MACSNP013040365827 chr9: 15294 TM2 Intergenic G A
homozygote
MACSNP013040365838 chr9: 15505 TM2 Intergenic A G
homozygote

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