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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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402414 SNVs 1 of 40242 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP015043964663 chr10: 460 SM1 Intergenic G A
homozygote
MACSNP015043964673 chr10: 680 SM1 Intergenic A G
homozygote
MACSNP015043964674 chr10: 717 SM1 Intergenic C T
homozygote
MACSNP015043964690 chr10: 867 SM1 Intergenic G A
homozygote
MACSNP015043964698 chr10: 983 SM1 Intergenic A G
homozygote
MACSNP015043964715 chr10: 2454 SM1 Intergenic G A
homozygote
MACSNP015043964721 chr10: 3531 SM1 Intergenic C T
homozygote
MACSNP015043964723 chr10: 3635 SM1 Intergenic T C
heterozygote
MACSNP015043964724 chr10: 3691 SM1 Intergenic T C
heterozygote
MACSNP015043964725 chr10: 3730 SM1 Intergenic T A
homozygote

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