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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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394775 SNVs 1 of 39478 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013053619619 chr13: 9281 TM2 Intergenic A G
homozygote
MACSNP013053619695 chr13: 18606 TM2 Intergenic T G
homozygote
MACSNP013053619696 chr13: 18702 TM2 Intergenic C T
homozygote
MACSNP013053619697 chr13: 18784 TM2 Intergenic T C
homozygote
MACSNP013053619698 chr13: 18826 TM2 Intergenic C A
homozygote
MACSNP013053619709 chr13: 19684 TM2 Intergenic C T
homozygote
MACSNP013053619710 chr13: 19833 TM2 Intergenic G A
homozygote
MACSNP013053619714 chr13: 19993 TM2 Intergenic A G
homozygote
MACSNP013053619717 chr13: 20101 TM2 Intergenic T G
homozygote
MACSNP013053619733 chr13: 20664 TM2 Intergenic C T
homozygote

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