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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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1067852 SNVs 1 of 106786 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020000000003 chr1: 9390 BM1 Intergenic G A
homozygote
MACSNP020000000005 chr1: 9428 BM1 Intergenic G T
homozygote
MACSNP020000000006 chr1: 9435 BM1 Intergenic C G
homozygote
MACSNP020000000010 chr1: 9596 BM1 Intergenic C A
homozygote
MACSNP020000000018 chr1: 9748 BM1 Intergenic A G
homozygote
MACSNP020000000021 chr1: 9800 BM1 Intergenic G C
homozygote
MACSNP020000000025 chr1: 9912 BM1 Intergenic T C
homozygote
MACSNP020000000031 chr1: 9979 BM1 Intergenic C T
heterozygote
MACSNP020000000035 chr1: 10109 BM1 Intergenic T C
homozygote
MACSNP020000000038 chr1: 10222 BM1 Intergenic T C
homozygote

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