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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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415808 SNVs 1 of 41581 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010065724290 chr17: 37540 CE4 Intergenic G A
heterozygote
MACSNP010065724291 chr17: 37548 CE4 Intergenic C T
heterozygote
MACSNP010065724296 chr17: 37610 CE4 Intergenic G A
heterozygote
MACSNP010065724298 chr17: 37654 CE4 Intergenic A G
homozygote
MACSNP010065724310 chr17: 37813 CE4 Intergenic T C
homozygote
MACSNP010065724330 chr17: 38006 CE4 Intergenic T C
homozygote
MACSNP010065724332 chr17: 38026 CE4 Intergenic T C
homozygote
MACSNP010065724336 chr17: 38086 CE4 Intergenic A T
heterozygote
MACSNP010065724351 chr17: 38201 CE4 Intergenic G C
homozygote
MACSNP010065724357 chr17: 38240 CE4 Intergenic T C
heterozygote

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