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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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328848 SNVs 1 of 32885 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006040365706 chr9: 3205 JM2 Intergenic A G
homozygote
MACSNP006040365778 chr9: 13967 JM2 Intergenic A G
homozygote
MACSNP006040365787 chr9: 14278 JM2 Intergenic G A
homozygote
MACSNP006040365795 chr9: 14439 JM2 Intergenic G A
homozygote
MACSNP006040365819 chr9: 15093 JM2 Intergenic G A
homozygote
MACSNP006040365848 chr9: 15777 JM2 Intergenic C T
homozygote
MACSNP006040365861 chr9: 16086 JM2 Intergenic A C
homozygote
MACSNP006040365864 chr9: 16130 JM2 Intergenic T C
homozygote
MACSNP006040365889 chr9: 17689 JM2 Intergenic G T
homozygote
MACSNP006040365911 chr9: 18462 JM2 Intergenic A C
homozygote

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