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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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356122 SNVs 1 of 35613 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016043964673 chr10: 680 SM2 Intergenic A G
homozygote
MACSNP016043964721 chr10: 3531 SM2 Intergenic C T
homozygote
MACSNP016043964725 chr10: 3730 SM2 Intergenic T A
homozygote
MACSNP016043964727 chr10: 3752 SM2 Intergenic T C
homozygote
MACSNP016043964731 chr10: 3974 SM2 Intergenic G A
homozygote
MACSNP016043964734 chr10: 4026 SM2 Intergenic C G
homozygote
MACSNP016043964737 chr10: 4068 SM2 Intergenic G A
heterozygote
MACSNP016043964740 chr10: 4196 SM2 Intergenic A T
homozygote
MACSNP016043964753 chr10: 4391 SM2 Intergenic G A
homozygote
MACSNP016043964754 chr10: 4417 SM2 Intergenic A G
homozygote

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