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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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243087 SNVs 1 of 24309 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP003068733175 chr18: 99 CR3 Intergenic G A
homozygote
MACSNP003068733181 chr18: 276 CR3 Intergenic A T
homozygote
MACSNP003068733183 chr18: 310 CR3 Intergenic A G
homozygote
MACSNP003068733189 chr18: 566 CR3 Intergenic G A
homozygote
MACSNP003068733190 chr18: 566 CR3 Intergenic G A
homozygote
MACSNP003068733205 chr18: 698 CR3 Intergenic A G
homozygote
MACSNP003068733206 chr18: 698 CR3 Intergenic A G
homozygote
MACSNP003068733217 chr18: 931 CR3 Intergenic C T
homozygote
MACSNP003068733233 chr18: 1614 CR3 Intergenic C T
homozygote
MACSNP003068733241 chr18: 1908 CR3 Intergenic C T
homozygote

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