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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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874193 SNVs 1 of 87420 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017026079066 chr6: 17623 PM1 Intergenic C T
homozygote
MACSNP017026079088 chr6: 24613 PM1 Intergenic C T
homozygote
MACSNP017026079090 chr6: 25025 PM1 Intergenic G C
homozygote
MACSNP017026079100 chr6: 26867 PM1 Intergenic G C
homozygote
MACSNP017026079107 chr6: 28178 PM1 Intergenic C T
homozygote
MACSNP017026079117 chr6: 30507 PM1 Intergenic G A
homozygote
MACSNP017026079127 chr6: 38929 PM1 Intergenic C T
homozygote
MACSNP017026079130 chr6: 39077 PM1 Intergenic T C
homozygote
MACSNP017026079138 chr6: 39787 PM1 Intergenic C A
homozygote
MACSNP017026079142 chr6: 40659 PM1 Intergenic G A
homozygote

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