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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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655756 SNVs 1 of 65576 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019031370894 chr7: 18980 LM1 Intergenic G A
homozygote
MACSNP019031370896 chr7: 19006 LM1 Intergenic A G
homozygote
MACSNP019031370898 chr7: 19018 LM1 Intergenic T C
homozygote
MACSNP019031370899 chr7: 19035 LM1 Intergenic C T
homozygote
MACSNP019031370900 chr7: 19042 LM1 Intergenic G C
homozygote
MACSNP019031370930 chr7: 25705 LM1 Intergenic T G
homozygote
MACSNP019031370977 chr7: 28865 LM1 Intergenic G C
heterozygote
MACSNP019031370981 chr7: 29053 LM1 Intergenic G A
heterozygote
MACSNP019031370985 chr7: 29205 LM1 Intergenic G A
heterozygote
MACSNP019031370989 chr7: 29282 LM1 Intergenic G T
homozygote

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