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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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295886 SNVs 1 of 29589 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001043964752 chr10: 4353 CR1 Intergenic C T
heterozygote
MACSNP001043964765 chr10: 4866 CR1 Intergenic A G
heterozygote
MACSNP001043964795 chr10: 5693 CR1 Intergenic A G
heterozygote
MACSNP001043964818 chr10: 6526 CR1 Intergenic G A
heterozygote
MACSNP001043964841 chr10: 7291 CR1 Intergenic T C
heterozygote
MACSNP001043964848 chr10: 7397 CR1 Intergenic C T
homozygote
MACSNP001043964853 chr10: 7549 CR1 Intergenic G A
homozygote
MACSNP001043964861 chr10: 7805 CR1 Intergenic T C
homozygote
MACSNP001043964881 chr10: 8393 CR1 Intergenic G C
heterozygote
MACSNP001043964883 chr10: 8566 CR1 Intergenic G T
heterozygote

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