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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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387224 SNVs 1 of 38723 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP003040365687 chr9: 2227 CR3 Intergenic C G
homozygote
MACSNP003040365706 chr9: 3205 CR3 Intergenic A G
homozygote
MACSNP003040365733 chr9: 4678 CR3 Intergenic T G
heterozygote
MACSNP003040365770 chr9: 12463 CR3 Intergenic T G
homozygote
MACSNP003040365773 chr9: 13037 CR3 Intergenic G C
homozygote
MACSNP003040365778 chr9: 13967 CR3 Intergenic A G
homozygote
MACSNP003040365787 chr9: 14278 CR3 Intergenic G A
homozygote
MACSNP003040365795 chr9: 14439 CR3 Intergenic G A
homozygote
MACSNP003040365799 chr9: 14536 CR3 Intergenic A G
heterozygote
MACSNP003040365834 chr9: 15396 CR3 Intergenic A T
heterozygote

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