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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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657265 SNVs 1 of 65727 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013020528812 chr5: 517 TM2 Intergenic A G
heterozygote
MACSNP013020528852 chr5: 21121 TM2 Intergenic T C
homozygote
MACSNP013020528866 chr5: 22565 TM2 Intergenic T C
homozygote
MACSNP013020528874 chr5: 23316 TM2 Intergenic A C
heterozygote
MACSNP013020528875 chr5: 23394 TM2 Intergenic G A
homozygote
MACSNP013020528879 chr5: 23463 TM2 Intergenic G A
heterozygote
MACSNP013020528880 chr5: 23497 TM2 Intergenic A C
heterozygote
MACSNP013020528889 chr5: 23916 TM2 Intergenic A G
heterozygote
MACSNP013020528890 chr5: 24045 TM2 Intergenic A G
heterozygote
MACSNP013020528897 chr5: 24823 TM2 Intergenic G A
homozygote

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