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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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292722 SNVs 1 of 29273 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018063857295 chr16: 951 PM2 Intergenic G A
heterozygote
MACSNP018063857301 chr16: 1077 PM2 Intergenic G C
homozygote
MACSNP018063857302 chr16: 1090 PM2 Intergenic T C
heterozygote
MACSNP018063857311 chr16: 1303 PM2 Intergenic G C
homozygote
MACSNP018063857315 chr16: 1369 PM2 Intergenic G A
homozygote
MACSNP018063857328 chr16: 1903 PM2 Intergenic T C
homozygote
MACSNP018063857334 chr16: 2246 PM2 Intergenic A G
homozygote
MACSNP018063857335 chr16: 2264 PM2 Intergenic A G
homozygote
MACSNP018063857338 chr16: 2378 PM2 Intergenic G A
homozygote
MACSNP018063857342 chr16: 2636 PM2 Intergenic T G
homozygote

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