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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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248593 SNVs 1 of 24860 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014063857290 chr16: 807 AM1 Intergenic T G
homozygote
MACSNP014063857294 chr16: 927 AM1 Intergenic G C
heterozygote
MACSNP014063857304 chr16: 1176 AM1 Intergenic T C
homozygote
MACSNP014063857322 chr16: 1683 AM1 Intergenic A G
homozygote
MACSNP014063857324 chr16: 1775 AM1 Intergenic T A
heterozygote
MACSNP014063857326 chr16: 1789 AM1 Intergenic G A
heterozygote
MACSNP014063857327 chr16: 1795 AM1 Intergenic A G
heterozygote
MACSNP014063857329 chr16: 2014 AM1 Intergenic G T
heterozygote
MACSNP014063857330 chr16: 2044 AM1 Intergenic T G
heterozygote
MACSNP014063857339 chr16: 2388 AM1 Intergenic C T
homozygote

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