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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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208074 SNVs 1 of 20808 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001063857289 chr16: 708 CR1 Intergenic C T
heterozygote
MACSNP001063857297 chr16: 997 CR1 Intergenic T C
heterozygote
MACSNP001063857309 chr16: 1242 CR1 Intergenic A C
heterozygote
MACSNP001063857318 chr16: 1557 CR1 Intergenic G A
heterozygote
MACSNP001063857337 chr16: 2360 CR1 Intergenic A C
heterozygote
MACSNP001063857343 chr16: 2639 CR1 Intergenic T C
heterozygote
MACSNP001063857366 chr16: 3735 CR1 Intergenic C T
heterozygote
MACSNP001063857367 chr16: 3822 CR1 Intergenic T C
heterozygote
MACSNP001063857384 chr16: 4772 CR1 Intergenic T G
heterozygote
MACSNP001063857385 chr16: 4779 CR1 Intergenic T C
heterozygote

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