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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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409325 SNVs 1 of 40933 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007065724298 chr17: 37654 CE1 Intergenic A G
heterozygote
MACSNP007065724299 chr17: 37677 CE1 Intergenic G A
heterozygote
MACSNP007065724305 chr17: 37752 CE1 Intergenic G A
heterozygote
MACSNP007065724309 chr17: 37778 CE1 Intergenic T C
heterozygote
MACSNP007065724313 chr17: 37841 CE1 Intergenic C T
heterozygote
MACSNP007065724314 chr17: 37854 CE1 Intergenic G A
heterozygote
MACSNP007065724320 chr17: 37929 CE1 Intergenic G A
heterozygote
MACSNP007065724322 chr17: 37946 CE1 Intergenic C A
homozygote
MACSNP007065724324 chr17: 37955 CE1 Intergenic G A
heterozygote
MACSNP007065724334 chr17: 38044 CE1 Intergenic T C
heterozygote

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