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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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374299 SNVs 1 of 37430 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019043964671 chr10: 654 LM1 Intergenic T G
homozygote
MACSNP019043964672 chr10: 667 LM1 Intergenic A G
homozygote
MACSNP019043964673 chr10: 680 LM1 Intergenic A G
homozygote
MACSNP019043964684 chr10: 809 LM1 Intergenic C T
homozygote
MACSNP019043964687 chr10: 857 LM1 Intergenic G A
homozygote
MACSNP019043964696 chr10: 956 LM1 Intergenic A G
homozygote
MACSNP019043964698 chr10: 983 LM1 Intergenic A G
homozygote
MACSNP019043964721 chr10: 3531 LM1 Intergenic C T
homozygote
MACSNP019043964727 chr10: 3752 LM1 Intergenic T C
homozygote
MACSNP019043964734 chr10: 4026 LM1 Intergenic C G
homozygote

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