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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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585108 SNVs 1 of 58511 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017040365688 chr9: 2422 PM1 Intergenic C T
homozygote
MACSNP017040365692 chr9: 2579 PM1 Intergenic T A
homozygote
MACSNP017040365697 chr9: 2812 PM1 Intergenic G A
heterozygote
MACSNP017040365703 chr9: 2893 PM1 Intergenic A G
homozygote
MACSNP017040365706 chr9: 3205 PM1 Intergenic A G
homozygote
MACSNP017040365709 chr9: 3224 PM1 Intergenic T C
heterozygote
MACSNP017040365712 chr9: 3325 PM1 Intergenic T C
homozygote
MACSNP017040365713 chr9: 3379 PM1 Intergenic G T
homozygote
MACSNP017040365715 chr9: 3851 PM1 Intergenic A G
homozygote
MACSNP017040365717 chr9: 3960 PM1 Intergenic C T
heterozygote

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