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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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633299 SNVs 1 of 63330 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020053619579 chr13: 1675 BM1 Intergenic A G
homozygote
MACSNP020053619724 chr13: 20220 BM1 Intergenic C T
homozygote
MACSNP020053619732 chr13: 20663 BM1 Intergenic C T
heterozygote
MACSNP020053619734 chr13: 20681 BM1 Intergenic A G
heterozygote
MACSNP020053619740 chr13: 20775 BM1 Intergenic G A
heterozygote
MACSNP020053619748 chr13: 20995 BM1 Intergenic G C
homozygote
MACSNP020053619844 chr13: 28055 BM1 Intergenic T C
homozygote
MACSNP020053619851 chr13: 28411 BM1 Intergenic C T
homozygote
MACSNP020053619855 chr13: 28576 BM1 Intergenic G T
homozygote
MACSNP020053619856 chr13: 28590 BM1 Intergenic C G
homozygote

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