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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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768608 SNVs 1 of 76861 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018031370925 chr7: 25484 PM2 Intergenic T C
homozygote
MACSNP018031370936 chr7: 25961 PM2 Intergenic G A
homozygote
MACSNP018031370938 chr7: 26115 PM2 Intergenic G T
homozygote
MACSNP018031370939 chr7: 26343 PM2 Intergenic A G
homozygote
MACSNP018031370947 chr7: 27294 PM2 Intergenic T C
homozygote
MACSNP018031370951 chr7: 27692 PM2 Intergenic C G
homozygote
MACSNP018031370965 chr7: 28412 PM2 Intergenic A T
heterozygote
MACSNP018031370971 chr7: 28645 PM2 Intergenic G C
heterozygote
MACSNP018031370972 chr7: 28684 PM2 Intergenic G A
heterozygote
MACSNP018031370992 chr7: 29412 PM2 Intergenic C T
homozygote

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