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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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272164 SNVs 1 of 27217 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002040365698 chr9: 2851 CR2 Intergenic T A
heterozygote
MACSNP002040365710 chr9: 3264 CR2 Intergenic G C
homozygote
MACSNP002040365727 chr9: 4322 CR2 Intergenic C T
homozygote
MACSNP002040365731 chr9: 4566 CR2 Intergenic T C
heterozygote
MACSNP002040365735 chr9: 5098 CR2 Intergenic T C
homozygote
MACSNP002040365739 chr9: 5826 CR2 Intergenic G T
heterozygote
MACSNP002040365769 chr9: 12418 CR2 Intergenic G A
heterozygote
MACSNP002040365774 chr9: 13339 CR2 Intergenic A T
homozygote
MACSNP002040365778 chr9: 13967 CR2 Intergenic A G
homozygote
MACSNP002040365784 chr9: 14224 CR2 Intergenic C T
homozygote

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