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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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492494 SNVs 1 of 49250 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011056871533 chr14: 3954 CE5 Intergenic A G
homozygote
MACSNP011056871551 chr14: 4684 CE5 Intergenic A T
homozygote
MACSNP011056871577 chr14: 5577 CE5 Intergenic C T
homozygote
MACSNP011056871580 chr14: 5697 CE5 Intergenic A T
homozygote
MACSNP011056871581 chr14: 5726 CE5 Intergenic T C
homozygote
MACSNP011056871589 chr14: 5898 CE5 Intergenic G A
homozygote
MACSNP011056871597 chr14: 6242 CE5 Intergenic T C
homozygote
MACSNP011056871604 chr14: 6463 CE5 Intergenic T C
homozygote
MACSNP011056871649 chr14: 8378 CE5 ENSMMUG00000011502: Intron
 C G
homozygote
MACSNP011056871659 chr14: 8928 CE5 ENSMMUG00000011502: Intron
 C T
homozygote

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