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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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475411 SNVs 1 of 47542 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004010706168 chr3: 6928 TW1 Intergenic A G
homozygote
MACSNP004010706183 chr3: 7656 TW1 Intergenic G A
homozygote
MACSNP004010706189 chr3: 8347 TW1 Intergenic A G
heterozygote
MACSNP004010706233 chr3: 11551 TW1 Intergenic C T
homozygote
MACSNP004010706252 chr3: 12286 TW1 Intergenic C T
homozygote
MACSNP004010706268 chr3: 12985 TW1 Intergenic G A
homozygote
MACSNP004010706287 chr3: 13576 TW1 Intergenic T C
heterozygote
MACSNP004010706291 chr3: 13841 TW1 Intergenic C T
homozygote
MACSNP004010706305 chr3: 14324 TW1 Intergenic C T
homozygote
MACSNP004010706323 chr3: 15005 TW1 Intergenic A C
heterozygote

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