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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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264402 SNVs 1 of 26441 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004043964762 chr10: 4752 TW1 Intergenic G A
heterozygote
MACSNP004043964790 chr10: 5568 TW1 Intergenic C T
heterozygote
MACSNP004043964822 chr10: 6669 TW1 Intergenic C A
heterozygote
MACSNP004043964828 chr10: 6926 TW1 Intergenic C A
heterozygote
MACSNP004043964834 chr10: 7030 TW1 Intergenic C T
heterozygote
MACSNP004043964851 chr10: 7482 TW1 Intergenic A C
heterozygote
MACSNP004043964853 chr10: 7549 TW1 Intergenic G A
homozygote
MACSNP004043964861 chr10: 7805 TW1 Intergenic T C
homozygote
MACSNP004043964867 chr10: 7933 TW1 Intergenic C T
heterozygote
MACSNP004043964880 chr10: 8386 TW1 Intergenic G T
heterozygote

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