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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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579788 SNVs 1 of 57979 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013010706168 chr3: 6928 TM2 Intergenic A G
homozygote
MACSNP013010706170 chr3: 6976 TM2 Intergenic G A
heterozygote
MACSNP013010706174 chr3: 7039 TM2 Intergenic G A
heterozygote
MACSNP013010706175 chr3: 7084 TM2 Intergenic A G
homozygote
MACSNP013010706181 chr3: 7473 TM2 Intergenic T G
homozygote
MACSNP013010706184 chr3: 7734 TM2 Intergenic A G
homozygote
MACSNP013010706210 chr3: 9738 TM2 Intergenic G A
homozygote
MACSNP013010706234 chr3: 11575 TM2 Intergenic T C
homozygote
MACSNP013010706239 chr3: 11780 TM2 Intergenic T C
homozygote
MACSNP013010706240 chr3: 11867 TM2 Intergenic G C
homozygote

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