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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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152470 SNVs 1 of 15247 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP003070912474 chr19: 27633 CR3 Intergenic A G
heterozygote
MACSNP003070912475 chr19: 27694 CR3 Intergenic A G
homozygote
MACSNP003070912478 chr19: 27867 CR3 Intergenic G A
heterozygote
MACSNP003070912492 chr19: 28259 CR3 Intergenic T C
heterozygote
MACSNP003070912516 chr19: 29339 CR3 Intergenic C G
heterozygote
MACSNP003070912523 chr19: 29498 CR3 Intergenic C T
heterozygote
MACSNP003070912549 chr19: 30045 CR3 Intergenic A G
homozygote
MACSNP003070912555 chr19: 30139 CR3 Intergenic T C
homozygote
MACSNP003070912573 chr19: 30680 CR3 Intergenic C T
heterozygote
MACSNP003070912587 chr19: 32938 CR3 Intergenic T G
heterozygote

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