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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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461203 SNVs 1 of 46121 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP008060569644 chr15: 1303 CE2 Intergenic G A
heterozygote
MACSNP008060569645 chr15: 1393 CE2 Intergenic G A
heterozygote
MACSNP008060569646 chr15: 1681 CE2 Intergenic G A
heterozygote
MACSNP008060569647 chr15: 1718 CE2 Intergenic T G
heterozygote
MACSNP008060569648 chr15: 1844 CE2 Intergenic C T
heterozygote
MACSNP008060569649 chr15: 1880 CE2 Intergenic T C
heterozygote
MACSNP008060569650 chr15: 3081 CE2 Intergenic G A
heterozygote
MACSNP008060569651 chr15: 3350 CE2 Intergenic G T
heterozygote
MACSNP008060569652 chr15: 3375 CE2 Intergenic C T
heterozygote
MACSNP008060569653 chr15: 3913 CE2 Intergenic C G
heterozygote

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