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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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487782 SNVs 1 of 48779 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017065724298 chr17: 37654 PM1 Intergenic A G
homozygote
MACSNP017065724301 chr17: 37694 PM1 Intergenic G C
heterozygote
MACSNP017065724312 chr17: 37826 PM1 Intergenic C T
heterozygote
MACSNP017065724343 chr17: 38135 PM1 Intergenic G A
heterozygote
MACSNP017065724347 chr17: 38164 PM1 Intergenic A G
heterozygote
MACSNP017065724360 chr17: 38248 PM1 Intergenic A G
heterozygote
MACSNP017065724370 chr17: 38413 PM1 Intergenic A G
heterozygote
MACSNP017065724389 chr17: 38555 PM1 Intergenic G A
heterozygote
MACSNP017065724393 chr17: 38587 PM1 Intergenic C G
heterozygote
MACSNP017065724394 chr17: 38598 PM1 Intergenic A G
heterozygote

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