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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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237885 SNVs 1 of 23789 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001068733177 chr18: 138 CR1 Intergenic A G
heterozygote
MACSNP001068733178 chr18: 182 CR1 Intergenic A G
homozygote
MACSNP001068733181 chr18: 276 CR1 Intergenic A T
homozygote
MACSNP001068733183 chr18: 310 CR1 Intergenic A G
homozygote
MACSNP001068733217 chr18: 931 CR1 Intergenic C T
homozygote
MACSNP001068733218 chr18: 952 CR1 Intergenic C T
heterozygote
MACSNP001068733237 chr18: 1846 CR1 Intergenic C T
heterozygote
MACSNP001068733248 chr18: 2220 CR1 Intergenic A G
homozygote
MACSNP001068733266 chr18: 2616 CR1 Intergenic G A
heterozygote
MACSNP001068733276 chr18: 2862 CR1 Intergenic A G
heterozygote

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