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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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463343 SNVs 1 of 46335 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014060569850 chr15: 34795 AM1 Intergenic A G
heterozygote
MACSNP014060569993 chr15: 47681 AM1 Intergenic A C
homozygote
MACSNP014060569999 chr15: 47889 AM1 Intergenic T A
homozygote
MACSNP014060570027 chr15: 49135 AM1 Intergenic G A
homozygote
MACSNP014060570046 chr15: 49402 AM1 Intergenic A G
homozygote
MACSNP014060570055 chr15: 49671 AM1 Intergenic T C
homozygote
MACSNP014060570058 chr15: 49711 AM1 Intergenic C A
homozygote
MACSNP014060570065 chr15: 49852 AM1 Intergenic A G
homozygote
MACSNP014060570075 chr15: 50083 AM1 Intergenic C T
heterozygote
MACSNP014060570106 chr15: 51612 AM1 Intergenic T C
heterozygote

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