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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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377630 SNVs 1 of 37763 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014043964721 chr10: 3531 AM1 Intergenic C T
homozygote
MACSNP014043964722 chr10: 3613 AM1 Intergenic T C
heterozygote
MACSNP014043964727 chr10: 3752 AM1 Intergenic T C
homozygote
MACSNP014043964730 chr10: 3950 AM1 Intergenic A C
heterozygote
MACSNP014043964731 chr10: 3974 AM1 Intergenic G A
homozygote
MACSNP014043964734 chr10: 4026 AM1 Intergenic C G
homozygote
MACSNP014043964735 chr10: 4046 AM1 Intergenic C T
heterozygote
MACSNP014043964736 chr10: 4067 AM1 Intergenic C A
heterozygote
MACSNP014043964738 chr10: 4076 AM1 Intergenic T C
heterozygote
MACSNP014043964741 chr10: 4246 AM1 Intergenic A G
homozygote

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