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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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484899 SNVs 1 of 48490 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018065724301 chr17: 37694 PM2 Intergenic G C
heterozygote
MACSNP018065724310 chr17: 37813 PM2 Intergenic T C
homozygote
MACSNP018065724339 chr17: 38109 PM2 Intergenic C G
heterozygote
MACSNP018065724343 chr17: 38135 PM2 Intergenic G A
heterozygote
MACSNP018065724347 chr17: 38164 PM2 Intergenic A G
heterozygote
MACSNP018065724349 chr17: 38172 PM2 Intergenic G A
heterozygote
MACSNP018065724353 chr17: 38216 PM2 Intergenic C G
heterozygote
MACSNP018065724358 chr17: 38241 PM2 Intergenic T C
heterozygote
MACSNP018065724360 chr17: 38248 PM2 Intergenic A G
heterozygote
MACSNP018065724361 chr17: 38256 PM2 Intergenic C T
heterozygote

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