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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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439888 SNVs 1 of 43989 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011053619571 chr13: 1413 CE5 Intergenic A C
heterozygote
MACSNP011053619576 chr13: 1609 CE5 Intergenic T C
heterozygote
MACSNP011053619584 chr13: 1834 CE5 Intergenic G T
homozygote
MACSNP011053619622 chr13: 9696 CE5 Intergenic A G
heterozygote
MACSNP011053619707 chr13: 19579 CE5 Intergenic G A
heterozygote
MACSNP011053619711 chr13: 19946 CE5 Intergenic C T
heterozygote
MACSNP011053619712 chr13: 19957 CE5 Intergenic A G
heterozygote
MACSNP011053619715 chr13: 20036 CE5 Intergenic A T
heterozygote
MACSNP011053619731 chr13: 20625 CE5 Intergenic T C
heterozygote
MACSNP011053619741 chr13: 20835 CE5 Intergenic T G
heterozygote

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