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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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579285 SNVs 1 of 57929 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018040365692 chr9: 2579 PM2 Intergenic T A
homozygote
MACSNP018040365697 chr9: 2812 PM2 Intergenic G A
heterozygote
MACSNP018040365712 chr9: 3325 PM2 Intergenic T C
homozygote
MACSNP018040365715 chr9: 3851 PM2 Intergenic A G
homozygote
MACSNP018040365717 chr9: 3960 PM2 Intergenic C T
heterozygote
MACSNP018040365720 chr9: 4206 PM2 Intergenic A C
homozygote
MACSNP018040365724 chr9: 4298 PM2 Intergenic T G
homozygote
MACSNP018040365726 chr9: 4318 PM2 Intergenic C A
heterozygote
MACSNP018040365729 chr9: 4408 PM2 Intergenic A G
heterozygote
MACSNP018040365746 chr9: 8358 PM2 Intergenic G C
heterozygote

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