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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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519461 SNVs 1 of 51947 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020043964670 chr10: 642 BM1 Intergenic T C
homozygote
MACSNP020043964673 chr10: 680 BM1 Intergenic A G
homozygote
MACSNP020043964703 chr10: 1162 BM1 Intergenic C A
homozygote
MACSNP020043964721 chr10: 3531 BM1 Intergenic C T
homozygote
MACSNP020043964723 chr10: 3635 BM1 Intergenic T C
homozygote
MACSNP020043964726 chr10: 3746 BM1 Intergenic A C
homozygote
MACSNP020043964727 chr10: 3752 BM1 Intergenic T C
homozygote
MACSNP020043964729 chr10: 3887 BM1 Intergenic G T
homozygote
MACSNP020043964732 chr10: 3985 BM1 Intergenic G A
homozygote
MACSNP020043964734 chr10: 4026 BM1 Intergenic C G
homozygote

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