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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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416618 SNVs 1 of 41662 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010053619584 chr13: 1834 CE4 Intergenic G T
homozygote
MACSNP010053619707 chr13: 19579 CE4 Intergenic G A
homozygote
MACSNP010053619711 chr13: 19946 CE4 Intergenic C T
homozygote
MACSNP010053619714 chr13: 19993 CE4 Intergenic A G
homozygote
MACSNP010053619718 chr13: 20116 CE4 Intergenic C T
heterozygote
MACSNP010053619721 chr13: 20194 CE4 Intergenic T G
heterozygote
MACSNP010053619722 chr13: 20202 CE4 Intergenic A G
heterozygote
MACSNP010053619731 chr13: 20625 CE4 Intergenic T C
heterozygote
MACSNP010053619732 chr13: 20663 CE4 Intergenic C T
heterozygote
MACSNP010053619740 chr13: 20775 CE4 Intergenic G A
heterozygote

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