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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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345785 SNVs 1 of 34579 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002010706135 chr3: 1386 CR2 Intergenic C G
heterozygote
MACSNP002010706138 chr3: 1585 CR2 Intergenic G A
heterozygote
MACSNP002010706193 chr3: 8490 CR2 Intergenic G A
heterozygote
MACSNP002010706268 chr3: 12985 CR2 Intergenic G A
heterozygote
MACSNP002010706274 chr3: 13096 CR2 Intergenic G T
heterozygote
MACSNP002010706331 chr3: 15306 CR2 Intergenic A G
heterozygote
MACSNP002010706381 chr3: 16730 CR2 Intergenic A G
heterozygote
MACSNP002010706392 chr3: 17059 CR2 Intergenic T C
heterozygote
MACSNP002010706420 chr3: 17774 CR2 Intergenic G C
heterozygote
MACSNP002010706441 chr3: 18446 CR2 Intergenic A G
heterozygote

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