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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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351817 SNVs 1 of 35182 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017068733181 chr18: 276 PM1 Intergenic A T
homozygote
MACSNP017068733198 chr18: 625 PM1 Intergenic T C
heterozygote
MACSNP017068733199 chr18: 625 PM1 Intergenic T C
heterozygote
MACSNP017068733200 chr18: 633 PM1 Intergenic G T
heterozygote
MACSNP017068733201 chr18: 633 PM1 Intergenic G T
heterozygote
MACSNP017068733209 chr18: 757 PM1 Intergenic C T
homozygote
MACSNP017068733210 chr18: 757 PM1 Intergenic C T
homozygote
MACSNP017068733211 chr18: 817 PM1 Intergenic A G
heterozygote
MACSNP017068733212 chr18: 817 PM1 Intergenic A G
heterozygote
MACSNP017068733217 chr18: 931 PM1 Intergenic C T
homozygote

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