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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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464959 SNVs 1 of 46496 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP012060569761 chr15: 32146 TM1 Intergenic G T
homozygote
MACSNP012060569762 chr15: 32201 TM1 Intergenic A C
homozygote
MACSNP012060569765 chr15: 32286 TM1 Intergenic A C
homozygote
MACSNP012060569766 chr15: 32298 TM1 Intergenic C G
homozygote
MACSNP012060569768 chr15: 32355 TM1 Intergenic C T
heterozygote
MACSNP012060569782 chr15: 32616 TM1 Intergenic A G
homozygote
MACSNP012060569784 chr15: 32697 TM1 Intergenic C A
homozygote
MACSNP012060569785 chr15: 32721 TM1 Intergenic T C
homozygote
MACSNP012060569801 chr15: 33831 TM1 Intergenic G C
homozygote
MACSNP012060569803 chr15: 33867 TM1 Intergenic G A
homozygote

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