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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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341094 SNVs 1 of 34110 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013043964673 chr10: 680 TM2 Intergenic A G
homozygote
MACSNP013043964721 chr10: 3531 TM2 Intergenic C T
homozygote
MACSNP013043964727 chr10: 3752 TM2 Intergenic T C
homozygote
MACSNP013043964731 chr10: 3974 TM2 Intergenic G A
homozygote
MACSNP013043964734 chr10: 4026 TM2 Intergenic C G
homozygote
MACSNP013043964741 chr10: 4246 TM2 Intergenic A G
homozygote
MACSNP013043964750 chr10: 4333 TM2 Intergenic A C
homozygote
MACSNP013043964754 chr10: 4417 TM2 Intergenic A G
homozygote
MACSNP013043964764 chr10: 4804 TM2 Intergenic G A
homozygote
MACSNP013043964777 chr10: 5313 TM2 Intergenic C T
homozygote

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