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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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426444 SNVs 1 of 42645 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016060569807 chr15: 34032 SM2 Intergenic A G
heterozygote
MACSNP016060569915 chr15: 37650 SM2 Intergenic T C
homozygote
MACSNP016060569917 chr15: 37725 SM2 Intergenic A G
homozygote
MACSNP016060570024 chr15: 49112 SM2 Intergenic C A
homozygote
MACSNP016060570048 chr15: 49447 SM2 Intergenic C T
homozygote
MACSNP016060570055 chr15: 49671 SM2 Intergenic T C
homozygote
MACSNP016060570058 chr15: 49711 SM2 Intergenic C A
homozygote
MACSNP016060570064 chr15: 49825 SM2 Intergenic T C
homozygote
MACSNP016060570065 chr15: 49852 SM2 Intergenic A G
homozygote
MACSNP016060570067 chr15: 49876 SM2 Intergenic T A
homozygote

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