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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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299188 SNVs 1 of 29919 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006053619734 chr13: 20681 JM2 Intergenic A G
heterozygote
MACSNP006053619898 chr13: 29795 JM2 Intergenic A T
homozygote
MACSNP006053619902 chr13: 29911 JM2 Intergenic C T
heterozygote
MACSNP006053619912 chr13: 30230 JM2 Intergenic G C
heterozygote
MACSNP006053619917 chr13: 30268 JM2 Intergenic G T
homozygote
MACSNP006053619922 chr13: 30399 JM2 Intergenic T C
homozygote
MACSNP006053619941 chr13: 31360 JM2 Intergenic G A
homozygote
MACSNP006053619955 chr13: 32036 JM2 Intergenic C T
heterozygote
MACSNP006053619994 chr13: 33375 JM2 Intergenic G A
heterozygote
MACSNP006053619997 chr13: 33491 JM2 Intergenic C T
homozygote

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