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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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521851 SNVs 1 of 52186 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006000000009 chr1: 9592 JM2 Intergenic A C
heterozygote
MACSNP006000000016 chr1: 9734 JM2 Intergenic T C
homozygote
MACSNP006000000019 chr1: 9773 JM2 Intergenic G A
homozygote
MACSNP006000000021 chr1: 9800 JM2 Intergenic G C
homozygote
MACSNP006000000033 chr1: 10053 JM2 Intergenic G A
heterozygote
MACSNP006000000051 chr1: 10493 JM2 Intergenic T C
heterozygote
MACSNP006000000056 chr1: 10569 JM2 Intergenic C T
homozygote
MACSNP006000000063 chr1: 10656 JM2 Intergenic G A
homozygote
MACSNP006000000070 chr1: 10885 JM2 Intergenic T C
homozygote
MACSNP006000000076 chr1: 10945 JM2 Intergenic G A
homozygote

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