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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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585737 SNVs 1 of 58574 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020065724290 chr17: 37540 BM1 Intergenic G A
heterozygote
MACSNP020065724291 chr17: 37548 BM1 Intergenic C T
heterozygote
MACSNP020065724292 chr17: 37555 BM1 Intergenic T A
heterozygote
MACSNP020065724293 chr17: 37583 BM1 Intergenic A G
heterozygote
MACSNP020065724294 chr17: 37590 BM1 Intergenic G C
heterozygote
MACSNP020065724298 chr17: 37654 BM1 Intergenic A G
homozygote
MACSNP020065724302 chr17: 37705 BM1 Intergenic A T
heterozygote
MACSNP020065724304 chr17: 37735 BM1 Intergenic C T
heterozygote
MACSNP020065724308 chr17: 37776 BM1 Intergenic C T
homozygote
MACSNP020065724310 chr17: 37813 BM1 Intergenic T C
homozygote

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