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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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431530 SNVs 1 of 43153 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006010706168 chr3: 6928 JM2 Intergenic A G
homozygote
MACSNP006010706169 chr3: 6939 JM2 Intergenic G A
heterozygote
MACSNP006010706195 chr3: 8548 JM2 Intergenic C T
homozygote
MACSNP006010706210 chr3: 9738 JM2 Intergenic G A
homozygote
MACSNP006010706241 chr3: 11894 JM2 Intergenic T G
heterozygote
MACSNP006010706264 chr3: 12740 JM2 Intergenic A T
homozygote
MACSNP006010706268 chr3: 12985 JM2 Intergenic G A
homozygote
MACSNP006010706305 chr3: 14324 JM2 Intergenic C T
homozygote
MACSNP006010706330 chr3: 15261 JM2 Intergenic T C
homozygote
MACSNP006010706349 chr3: 15741 JM2 Intergenic A T
heterozygote

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