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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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220857 SNVs 1 of 22086 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002065724298 chr17: 37654 CR2 Intergenic A G
heterozygote
MACSNP002065724309 chr17: 37778 CR2 Intergenic T C
heterozygote
MACSNP002065724310 chr17: 37813 CR2 Intergenic T C
homozygote
MACSNP002065724313 chr17: 37841 CR2 Intergenic C T
heterozygote
MACSNP002065724316 chr17: 37873 CR2 Intergenic G A
homozygote
MACSNP002065724330 chr17: 38006 CR2 Intergenic T C
homozygote
MACSNP002065724342 chr17: 38130 CR2 Intergenic A T
heterozygote
MACSNP002065724351 chr17: 38201 CR2 Intergenic G C
homozygote
MACSNP002065724356 chr17: 38234 CR2 Intergenic G A
heterozygote
MACSNP002065724359 chr17: 38243 CR2 Intergenic C T
heterozygote

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