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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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409598 SNVs 1 of 40960 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001046690003 chr11: 76 CR1 Intergenic A G
homozygote
MACSNP001046690011 chr11: 270 CR1 Intergenic T C
homozygote
MACSNP001046690012 chr11: 326 CR1 Intergenic T C
homozygote
MACSNP001046690014 chr11: 361 CR1 Intergenic G A
homozygote
MACSNP001046690016 chr11: 410 CR1 Intergenic A G
homozygote
MACSNP001046690018 chr11: 453 CR1 Intergenic G A
homozygote
MACSNP001046690019 chr11: 562 CR1 Intergenic G A
homozygote
MACSNP001046690021 chr11: 575 CR1 Intergenic A G
heterozygote
MACSNP001046690026 chr11: 745 CR1 Intergenic G A
heterozygote
MACSNP001046690029 chr11: 805 CR1 Intergenic C T
homozygote

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