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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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299090 SNVs 1 of 29909 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP003043964677 chr10: 746 CR3 Intergenic A T
heterozygote
MACSNP003043964707 chr10: 1526 CR3 Intergenic T A
heterozygote
MACSNP003043964712 chr10: 2084 CR3 Intergenic G A
heterozygote
MACSNP003043964728 chr10: 3865 CR3 Intergenic C T
heterozygote
MACSNP003043964740 chr10: 4196 CR3 Intergenic A T
heterozygote
MACSNP003043964748 chr10: 4298 CR3 Intergenic G T
heterozygote
MACSNP003043964749 chr10: 4330 CR3 Intergenic G A
heterozygote
MACSNP003043964752 chr10: 4353 CR3 Intergenic C T
heterozygote
MACSNP003043964766 chr10: 4873 CR3 Intergenic G T
heterozygote
MACSNP003043964853 chr10: 7549 CR3 Intergenic G A
homozygote

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