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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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297784 SNVs 1 of 29779 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017063857301 chr16: 1077 PM1 Intergenic G C
heterozygote
MACSNP017063857309 chr16: 1242 PM1 Intergenic A C
homozygote
MACSNP017063857315 chr16: 1369 PM1 Intergenic G A
homozygote
MACSNP017063857319 chr16: 1601 PM1 Intergenic G A
heterozygote
MACSNP017063857328 chr16: 1903 PM1 Intergenic T C
homozygote
MACSNP017063857334 chr16: 2246 PM1 Intergenic A G
homozygote
MACSNP017063857335 chr16: 2264 PM1 Intergenic A G
homozygote
MACSNP017063857338 chr16: 2378 PM1 Intergenic G A
homozygote
MACSNP017063857342 chr16: 2636 PM1 Intergenic T G
heterozygote
MACSNP017063857348 chr16: 2981 PM1 Intergenic T A
heterozygote

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