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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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547263 SNVs 1 of 54727 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014046690011 chr11: 270 AM1 Intergenic T C
homozygote
MACSNP014046690022 chr11: 630 AM1 Intergenic G A
homozygote
MACSNP014046690039 chr11: 1070 AM1 Intergenic C T
heterozygote
MACSNP014046690042 chr11: 1220 AM1 Intergenic C T
homozygote
MACSNP014046690047 chr11: 1335 AM1 Intergenic C G
homozygote
MACSNP014046690068 chr11: 2121 AM1 Intergenic G A
heterozygote
MACSNP014046690078 chr11: 2352 AM1 Intergenic C A
heterozygote
MACSNP014046690121 chr11: 3289 AM1 Intergenic T C
heterozygote
MACSNP014046690128 chr11: 3462 AM1 Intergenic G T
heterozygote
MACSNP014046690178 chr11: 5013 AM1 Intergenic G A
heterozygote

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