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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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356697 SNVs 1 of 35670 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP003060569699 chr15: 17080 CR3 Intergenic A G
heterozygote
MACSNP003060569700 chr15: 17111 CR3 Intergenic T C
heterozygote
MACSNP003060569762 chr15: 32201 CR3 Intergenic A C
heterozygote
MACSNP003060569765 chr15: 32286 CR3 Intergenic A C
heterozygote
MACSNP003060569773 chr15: 32508 CR3 Intergenic G A
heterozygote
MACSNP003060569774 chr15: 32516 CR3 Intergenic C T
heterozygote
MACSNP003060569778 chr15: 32570 CR3 Intergenic T A
heterozygote
MACSNP003060569782 chr15: 32616 CR3 Intergenic A G
homozygote
MACSNP003060569784 chr15: 32697 CR3 Intergenic C A
heterozygote
MACSNP003060569785 chr15: 32721 CR3 Intergenic T C
heterozygote

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