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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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332511 SNVs 1 of 33252 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001053619681 chr13: 16581 CR1 Intergenic C T
heterozygote
MACSNP001053619683 chr13: 16661 CR1 Intergenic T C
heterozygote
MACSNP001053619691 chr13: 17587 CR1 Intergenic G A
heterozygote
MACSNP001053619713 chr13: 19992 CR1 Intergenic C T
heterozygote
MACSNP001053619726 chr13: 20449 CR1 Intergenic A C
heterozygote
MACSNP001053619738 chr13: 20767 CR1 Intergenic T G
homozygote
MACSNP001053619739 chr13: 20774 CR1 Intergenic C T
heterozygote
MACSNP001053619744 chr13: 20911 CR1 Intergenic C A
heterozygote
MACSNP001053619748 chr13: 20995 CR1 Intergenic G C
homozygote
MACSNP001053619749 chr13: 21014 CR1 Intergenic A G
heterozygote

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