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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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728667 SNVs 1 of 72867 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011026079066 chr6: 17623 CE5 Intergenic C T
heterozygote
MACSNP011026079076 chr6: 23595 CE5 Intergenic A T
heterozygote
MACSNP011026079096 chr6: 25707 CE5 Intergenic C T
heterozygote
MACSNP011026079110 chr6: 28795 CE5 Intergenic A T
homozygote
MACSNP011026079116 chr6: 30333 CE5 Intergenic A G
heterozygote
MACSNP011026079118 chr6: 30945 CE5 Intergenic A G
heterozygote
MACSNP011026079127 chr6: 38929 CE5 Intergenic C T
homozygote
MACSNP011026079130 chr6: 39077 CE5 Intergenic T C
homozygote
MACSNP011026079135 chr6: 39552 CE5 Intergenic T A
homozygote
MACSNP011026079137 chr6: 39682 CE5 Intergenic A G
heterozygote

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