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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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301716 SNVs 1 of 30172 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007068733181 chr18: 276 CE1 Intergenic A T
homozygote
MACSNP007068733183 chr18: 310 CE1 Intergenic A G
homozygote
MACSNP007068733185 chr18: 387 CE1 Intergenic A G
homozygote
MACSNP007068733217 chr18: 931 CE1 Intergenic C T
homozygote
MACSNP007068733244 chr18: 2051 CE1 Intergenic T C
homozygote
MACSNP007068733248 chr18: 2220 CE1 Intergenic A G
homozygote
MACSNP007068733261 chr18: 2532 CE1 Intergenic G A
homozygote
MACSNP007068733269 chr18: 2752 CE1 Intergenic T G
homozygote
MACSNP007068733273 chr18: 2807 CE1 Intergenic T C
homozygote
MACSNP007068733293 chr18: 3450 CE1 Intergenic C T
heterozygote

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