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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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624207 SNVs 1 of 62421 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016010706168 chr3: 6928 SM2 Intergenic A G
homozygote
MACSNP016010706174 chr3: 7039 SM2 Intergenic G A
homozygote
MACSNP016010706175 chr3: 7084 SM2 Intergenic A G
homozygote
MACSNP016010706181 chr3: 7473 SM2 Intergenic T G
homozygote
MACSNP016010706210 chr3: 9738 SM2 Intergenic G A
homozygote
MACSNP016010706236 chr3: 11625 SM2 Intergenic A T
homozygote
MACSNP016010706266 chr3: 12835 SM2 Intergenic A G
homozygote
MACSNP016010706268 chr3: 12985 SM2 Intergenic G A
homozygote
MACSNP016010706280 chr3: 13288 SM2 Intergenic T C
homozygote
MACSNP016010706286 chr3: 13556 SM2 Intergenic C T
homozygote

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