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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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602537 SNVs 1 of 60254 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018056871533 chr14: 3954 PM2 Intergenic A G
homozygote
MACSNP018056871539 chr14: 4190 PM2 Intergenic G A
homozygote
MACSNP018056871543 chr14: 4449 PM2 Intergenic C T
heterozygote
MACSNP018056871544 chr14: 4478 PM2 Intergenic C T
homozygote
MACSNP018056871551 chr14: 4684 PM2 Intergenic A T
homozygote
MACSNP018056871559 chr14: 4939 PM2 Intergenic T C
homozygote
MACSNP018056871563 chr14: 5042 PM2 Intergenic T C
heterozygote
MACSNP018056871564 chr14: 5121 PM2 Intergenic A C
heterozygote
MACSNP018056871566 chr14: 5319 PM2 Intergenic C T
heterozygote
MACSNP018056871568 chr14: 5398 PM2 Intergenic G T
heterozygote

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