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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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149391 SNVs 1 of 14940 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001070912492 chr19: 28259 CR1 Intergenic T C
heterozygote
MACSNP001070912508 chr19: 28571 CR1 Intergenic A G
heterozygote
MACSNP001070912516 chr19: 29339 CR1 Intergenic C G
heterozygote
MACSNP001070912549 chr19: 30045 CR1 Intergenic A G
homozygote
MACSNP001070912555 chr19: 30139 CR1 Intergenic T C
homozygote
MACSNP001070912586 chr19: 30981 CR1 Intergenic T C
heterozygote
MACSNP001070912603 chr19: 33491 CR1 Intergenic A G
heterozygote
MACSNP001070912607 chr19: 33526 CR1 Intergenic A G
homozygote
MACSNP001070912609 chr19: 33571 CR1 Intergenic A G
heterozygote
MACSNP001070912614 chr19: 33682 CR1 Intergenic T C
homozygote

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